PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 2557841-1 1989 Treatment of human platelets with concentrations of benzyl alcohol up to 50 mM augmented adenylate cyclase activity when it was assayed in the basal state and when stimulated by prostaglandin E1 (PGE1), isoprenaline or NaF. Benzyl Alcohol 52-66 C-X-C motif chemokine ligand 8 Homo sapiens 219-222 2686646-2 1989 Potent inhibition of IL-8-induced migration was observed in response to nifedipine (IC50 = 10 nM), verapamil (IC50 = 60 nM) and diltiazem (IC50 = 10 nM). Nifedipine 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 2686646-2 1989 Potent inhibition of IL-8-induced migration was observed in response to nifedipine (IC50 = 10 nM), verapamil (IC50 = 60 nM) and diltiazem (IC50 = 10 nM). Verapamil 99-108 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 2686646-2 1989 Potent inhibition of IL-8-induced migration was observed in response to nifedipine (IC50 = 10 nM), verapamil (IC50 = 60 nM) and diltiazem (IC50 = 10 nM). Diltiazem 128-137 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 2478657-0 1989 The neutrophil-activating peptide NAF/NAP-1 induces histamine and leukotriene release by interleukin 3-primed basophils. Histamine 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 2681204-2 1989 The 1H-NMR spectrum of IL-8 is assigned in a sequential manner and regular elements of secondary structure are identified on the basis of a qualitative interpretation of the nuclear Overhauser, coupling constant and amide exchange data. Hydrogen 4-6 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 2681204-4 1989 It is shown that IL-8 is a dimer in solution in which the interface is principally formed by six backbone hydrogen bonds between residues 25, 27, and 29 of one monomer and residues 29, 27, and 25, respectively, of the other. Hydrogen 106-114 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 2478657-0 1989 The neutrophil-activating peptide NAF/NAP-1 induces histamine and leukotriene release by interleukin 3-primed basophils. Histamine 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 2478657-0 1989 The neutrophil-activating peptide NAF/NAP-1 induces histamine and leukotriene release by interleukin 3-primed basophils. Leukotrienes 66-77 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 2549106-1 1989 This report reviews the methods and findings of published clinical studies comparing dentifrices containing sodium fluoride (NaF) and sodium monofluorophosphate (Na2PO3F) for the purpose of determining whether sodium fluoride formulations have superior cariostatic effects. Sodium Fluoride 108-123 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 2478657-0 1989 The neutrophil-activating peptide NAF/NAP-1 induces histamine and leukotriene release by interleukin 3-primed basophils. Leukotrienes 66-77 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 2478657-2 1989 This study demonstrates that after exposure to IL-3, basophils release histamine and leukotrienes in response to the neutrophil-activating peptide NAF/NAP-1. Histamine 71-80 C-X-C motif chemokine ligand 8 Homo sapiens 147-150 2478657-2 1989 This study demonstrates that after exposure to IL-3, basophils release histamine and leukotrienes in response to the neutrophil-activating peptide NAF/NAP-1. Histamine 71-80 C-X-C motif chemokine ligand 8 Homo sapiens 151-156 2478657-2 1989 This study demonstrates that after exposure to IL-3, basophils release histamine and leukotrienes in response to the neutrophil-activating peptide NAF/NAP-1. Leukotrienes 85-97 C-X-C motif chemokine ligand 8 Homo sapiens 147-150 2478657-2 1989 This study demonstrates that after exposure to IL-3, basophils release histamine and leukotrienes in response to the neutrophil-activating peptide NAF/NAP-1. Leukotrienes 85-97 C-X-C motif chemokine ligand 8 Homo sapiens 151-156 2560871-5 1989 After administration of sulprostone the adenylate cyclase activity was decreased 3- and 4.5-fold in response to specific stimulators NaF and forskolin, respectively, thus indicating that content and activity of G protein, and apparently of catalytic subunits, were decreased. sulprostone 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 133-136 2677006-1 1989 The interaction of 125I-labeled recombinant human neutrophil activating factor (NAF) with polymorphonuclear leukocytes (PMN) was studied by means of a radioreceptor assay. Iodine-125 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 50-78 2677006-1 1989 The interaction of 125I-labeled recombinant human neutrophil activating factor (NAF) with polymorphonuclear leukocytes (PMN) was studied by means of a radioreceptor assay. Iodine-125 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 2677006-3 1989 Internalized iodinated NAF was processed into trichloroacetic acid-soluble forms. Trichloroacetic Acid 46-66 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 2675839-2 1989 Native LUCT and LU10 specifically induced the phosphorylation of 64 kD protein of PMN, and serine residue in the 64 kD protein was major phosphorylated amino acid. Serine 91-97 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 2675839-3 1989 Furthermore, native LUCT enhanced the release of myeloperoxidase and beta-glucuronidase from PMN in the presence of cytochalasin B and FMLP, but LU10 did not. Cytochalasin B 116-130 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 2504305-5 1989 Markedly increased levels of GM-CSF mRNA occurred in these cells after exposure to sodium fluoride (NaF) and the effect of NaF was slightly enhanced by aluminum chloride; these results suggest that accumulation of GM-CSF mRNA can occur by activating a G-binding protein. Aluminum Chloride 152-169 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 2561629-4 1989 The combination consisting of 0.3% triclosan/2% PVM/MA copolymer/1100 ppm NaF was found to be highly effective on reducing smooth and fissure caries, and plaque extent compared to to 1100 ppm/NaF by itself in rats when applied topically. Triclosan 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 2561629-4 1989 The combination consisting of 0.3% triclosan/2% PVM/MA copolymer/1100 ppm NaF was found to be highly effective on reducing smooth and fissure caries, and plaque extent compared to to 1100 ppm/NaF by itself in rats when applied topically. copolymer 55-64 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 2638180-6 1989 It was concluded that the 0.3% triclosan/PVM/MA copolymer/NaF test dentifrice provided effective delivery and bioavailability of the antiplaque agent, triclosan. Triclosan 151-160 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 2547872-2 1989 Previous studies demonstrating hydrolysis of phosphatidylinositol bisphosphate (PIP2) and generation of inositol phosphates in neutrophils exposed to 20.0 mM NaF provide indirect evidence that activation of phospholipase-associated guanine nucleotide regulatory protein, a guanine nucleotide binding protein which regulates the activation of a membrane inositol-specific phospholipase C, is an early event in the neutrophil stimulus-response pathway triggered by fluoride. phosphatidylinositol bisphosphate 45-78 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 2547872-2 1989 Previous studies demonstrating hydrolysis of phosphatidylinositol bisphosphate (PIP2) and generation of inositol phosphates in neutrophils exposed to 20.0 mM NaF provide indirect evidence that activation of phospholipase-associated guanine nucleotide regulatory protein, a guanine nucleotide binding protein which regulates the activation of a membrane inositol-specific phospholipase C, is an early event in the neutrophil stimulus-response pathway triggered by fluoride. Phosphates 113-123 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 2547872-2 1989 Previous studies demonstrating hydrolysis of phosphatidylinositol bisphosphate (PIP2) and generation of inositol phosphates in neutrophils exposed to 20.0 mM NaF provide indirect evidence that activation of phospholipase-associated guanine nucleotide regulatory protein, a guanine nucleotide binding protein which regulates the activation of a membrane inositol-specific phospholipase C, is an early event in the neutrophil stimulus-response pathway triggered by fluoride. Phosphatidylinositol 4,5-Diphosphate 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 2788065-2 1989 One hundred and forty-two children, of whom 56 had participated in a fluoride tablet program of 0.5/1.0 mg NaF per day were examined blindly for possible fluoride-induced enamel changes. Fluorides 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 2547872-2 1989 Previous studies demonstrating hydrolysis of phosphatidylinositol bisphosphate (PIP2) and generation of inositol phosphates in neutrophils exposed to 20.0 mM NaF provide indirect evidence that activation of phospholipase-associated guanine nucleotide regulatory protein, a guanine nucleotide binding protein which regulates the activation of a membrane inositol-specific phospholipase C, is an early event in the neutrophil stimulus-response pathway triggered by fluoride. Fluorides 463-471 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 2547872-3 1989 Consistent with this hypothesis, exposure of a plasma membrane rich preparation isolated from 32P labeled neutrophils to 20.0 mM NaF resulted in hydrolysis of labeled PIP2. Phosphorus-32 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 2547872-3 1989 Consistent with this hypothesis, exposure of a plasma membrane rich preparation isolated from 32P labeled neutrophils to 20.0 mM NaF resulted in hydrolysis of labeled PIP2. Phosphatidylinositol 4,5-Diphosphate 167-171 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 2549166-0 1989 The monocyte-derived neutrophil activating peptide (NAP/interleukin 8) stimulates human neutrophil arachidonate-5-lipoxygenase, but not the release of cellular arachidonate. Arachidonic Acid 99-111 C-X-C motif chemokine ligand 8 Homo sapiens 4-50 2549166-0 1989 The monocyte-derived neutrophil activating peptide (NAP/interleukin 8) stimulates human neutrophil arachidonate-5-lipoxygenase, but not the release of cellular arachidonate. Arachidonic Acid 99-111 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 2476383-0 1989 Neutrophil attractant/activation protein-1 (NAP-1) causes human basophil histamine release. Histamine 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 0-42 2510716-3 1989 In the present study, we have attempted to locate the site of action of phorbol ester by comparing thrombin-induced (i.e. receptor-mediated) platelet activation with that induced by guanosine 5"-[gamma-thio]triphosphate (GTP[S]) and NaF, two agents which by-pass the receptor and initiate platelet responses by directly modulating G-protein function. Phorbol Esters 72-85 C-X-C motif chemokine ligand 8 Homo sapiens 233-236 2510716-4 1989 After a 10 s pre-treatment with PMA (16 nM), dense-granule secretion induced by thrombin (0.2 unit/ml), GTP[S] (40 microM) and NaF (30 mM) was potentiated, resulting in a greater than additive response to agent plus PMA. Tetradecanoylphorbol Acetate 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 2510716-4 1989 After a 10 s pre-treatment with PMA (16 nM), dense-granule secretion induced by thrombin (0.2 unit/ml), GTP[S] (40 microM) and NaF (30 mM) was potentiated, resulting in a greater than additive response to agent plus PMA. Tetradecanoylphorbol Acetate 216-219 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 2510716-5 1989 However, after a 5 min pre-treatment, thrombin-induced secretion alone was inhibited, whereas PMA plus GTP[S]/NaF-induced release remained greater than additive. Guanosine Triphosphate 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 2776689-1 1989 Exposure of fresh water crab Barytelphusa querini to a sublethal concentration of NaF (30 ppm) caused significant alterations in the carbohydrate metabolism. Carbohydrates 133-145 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 2476383-1 1989 Basophils from five of six human donors released histamine in response to neutrophil attractant/activation protein-1 (NAP-1). Histamine 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 2476383-0 1989 Neutrophil attractant/activation protein-1 (NAP-1) causes human basophil histamine release. Histamine 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 44-49 2510716-7 1989 That secretion induced by these agents is a protein kinase C-dependent event was demonstrable by using staurosporine, a protein kinase C inhibitor which at concentrations of 1-10 nM inhibited (70-90%) PMA-induced as well as thrombin- and NaF-induced secretion and protein phosphorylation. Staurosporine 103-116 C-X-C motif chemokine ligand 8 Homo sapiens 238-241 2510716-7 1989 That secretion induced by these agents is a protein kinase C-dependent event was demonstrable by using staurosporine, a protein kinase C inhibitor which at concentrations of 1-10 nM inhibited (70-90%) PMA-induced as well as thrombin- and NaF-induced secretion and protein phosphorylation. Tetradecanoylphorbol Acetate 201-204 C-X-C motif chemokine ligand 8 Homo sapiens 238-241 2476383-1 1989 Basophils from five of six human donors released histamine in response to neutrophil attractant/activation protein-1 (NAP-1). Histamine 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 74-116 2746239-8 1989 Preincubation of aluminum with citrate, NADP+, EDTA, NaF, ATP, and apotransferrin protected the G6PD isozymes against aluminum inactivation. Aluminum 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 2768695-1 1989 This study determined the effect of brushing with 0.4% stannous fluoride (SnF2) or 0.22% sodium fluoride (NaF) on clinical and microbial parameters associated with gingivitis. Sodium Fluoride 89-104 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 2746239-8 1989 Preincubation of aluminum with citrate, NADP+, EDTA, NaF, ATP, and apotransferrin protected the G6PD isozymes against aluminum inactivation. Aluminum 118-126 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 2746239-10 1989 The dissociation constants for the enzyme-aluminum complex of the isozymes varied from 2 to 4 microM, as measured by using NaF, a known chelator for aluminum. Aluminum 42-50 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 2746239-10 1989 The dissociation constants for the enzyme-aluminum complex of the isozymes varied from 2 to 4 microM, as measured by using NaF, a known chelator for aluminum. Aluminum 149-157 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 2659722-1 1989 A chemotactic protein for polymorphonuclear leukocytes (lung carcinoma-derived chemotaxin [LUCT]) was purified from culture fluid of the human lung giant cell carcinoma LU65C cells to electrophoretically homogeneous form through five sequential purification steps: DEAE-Sepharose, CM-Sepharose, HPLC on carboxyl-methylated-polyvinylalcohol resin, hydrophobic, and reversed-phase. deae-sepharose 265-279 C-X-C motif chemokine ligand 8 Homo sapiens 56-89 2668365-1 1989 A three-year clinical trial was conducted to determine whether a sodium fluoride (NaF) dentifrice had greater cariostatic effects than a sodium monofluorophosphate (Na2PO3F) dentifrice. Sodium Fluoride 65-80 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 2662972-6 1989 Amino acid composition of CINC showed that CINC has a resemblance to human monocyte-derived neutrophil chemotactic factor (MDNCF) rather than human complement fragment, C5a. Zinc 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 75-121 2662972-6 1989 Amino acid composition of CINC showed that CINC has a resemblance to human monocyte-derived neutrophil chemotactic factor (MDNCF) rather than human complement fragment, C5a. Zinc 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 75-121 2662972-6 1989 Amino acid composition of CINC showed that CINC has a resemblance to human monocyte-derived neutrophil chemotactic factor (MDNCF) rather than human complement fragment, C5a. Zinc 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 2550298-6 1989 NaF (20 mM) mimicked the stimulatory effect of PGF2 alpha on inositol phosphate accumulation suggesting the involvement of a guanine nucleotide regulatory protein in the activation of phospholipase C. In contrast, hCG but not PGF2 alpha or NaF stimulated cAMP accumulation in 30 min incubations. Dinoprost 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2550298-6 1989 NaF (20 mM) mimicked the stimulatory effect of PGF2 alpha on inositol phosphate accumulation suggesting the involvement of a guanine nucleotide regulatory protein in the activation of phospholipase C. In contrast, hCG but not PGF2 alpha or NaF stimulated cAMP accumulation in 30 min incubations. Dinoprost 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 240-243 2550298-6 1989 NaF (20 mM) mimicked the stimulatory effect of PGF2 alpha on inositol phosphate accumulation suggesting the involvement of a guanine nucleotide regulatory protein in the activation of phospholipase C. In contrast, hCG but not PGF2 alpha or NaF stimulated cAMP accumulation in 30 min incubations. Inositol Phosphates 61-79 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2550298-6 1989 NaF (20 mM) mimicked the stimulatory effect of PGF2 alpha on inositol phosphate accumulation suggesting the involvement of a guanine nucleotide regulatory protein in the activation of phospholipase C. In contrast, hCG but not PGF2 alpha or NaF stimulated cAMP accumulation in 30 min incubations. Dinoprost 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2550298-6 1989 NaF (20 mM) mimicked the stimulatory effect of PGF2 alpha on inositol phosphate accumulation suggesting the involvement of a guanine nucleotide regulatory protein in the activation of phospholipase C. In contrast, hCG but not PGF2 alpha or NaF stimulated cAMP accumulation in 30 min incubations. Dinoprost 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 240-243 2550298-6 1989 NaF (20 mM) mimicked the stimulatory effect of PGF2 alpha on inositol phosphate accumulation suggesting the involvement of a guanine nucleotide regulatory protein in the activation of phospholipase C. In contrast, hCG but not PGF2 alpha or NaF stimulated cAMP accumulation in 30 min incubations. Cyclic AMP 255-259 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 9992051-0 1989 Spin-multiplet electronic transition energies in NaF:Cu+ by the self-interaction-corrected local-spin-density approximation. Copper 53-55 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 2659722-1 1989 A chemotactic protein for polymorphonuclear leukocytes (lung carcinoma-derived chemotaxin [LUCT]) was purified from culture fluid of the human lung giant cell carcinoma LU65C cells to electrophoretically homogeneous form through five sequential purification steps: DEAE-Sepharose, CM-Sepharose, HPLC on carboxyl-methylated-polyvinylalcohol resin, hydrophobic, and reversed-phase. deae-sepharose 265-279 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 2659722-1 1989 A chemotactic protein for polymorphonuclear leukocytes (lung carcinoma-derived chemotaxin [LUCT]) was purified from culture fluid of the human lung giant cell carcinoma LU65C cells to electrophoretically homogeneous form through five sequential purification steps: DEAE-Sepharose, CM-Sepharose, HPLC on carboxyl-methylated-polyvinylalcohol resin, hydrophobic, and reversed-phase. Curium 281-284 C-X-C motif chemokine ligand 8 Homo sapiens 56-89 2659722-1 1989 A chemotactic protein for polymorphonuclear leukocytes (lung carcinoma-derived chemotaxin [LUCT]) was purified from culture fluid of the human lung giant cell carcinoma LU65C cells to electrophoretically homogeneous form through five sequential purification steps: DEAE-Sepharose, CM-Sepharose, HPLC on carboxyl-methylated-polyvinylalcohol resin, hydrophobic, and reversed-phase. Curium 281-284 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 2659722-1 1989 A chemotactic protein for polymorphonuclear leukocytes (lung carcinoma-derived chemotaxin [LUCT]) was purified from culture fluid of the human lung giant cell carcinoma LU65C cells to electrophoretically homogeneous form through five sequential purification steps: DEAE-Sepharose, CM-Sepharose, HPLC on carboxyl-methylated-polyvinylalcohol resin, hydrophobic, and reversed-phase. Sepharose 270-279 C-X-C motif chemokine ligand 8 Homo sapiens 56-89 2659722-1 1989 A chemotactic protein for polymorphonuclear leukocytes (lung carcinoma-derived chemotaxin [LUCT]) was purified from culture fluid of the human lung giant cell carcinoma LU65C cells to electrophoretically homogeneous form through five sequential purification steps: DEAE-Sepharose, CM-Sepharose, HPLC on carboxyl-methylated-polyvinylalcohol resin, hydrophobic, and reversed-phase. Sepharose 270-279 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 2659722-1 1989 A chemotactic protein for polymorphonuclear leukocytes (lung carcinoma-derived chemotaxin [LUCT]) was purified from culture fluid of the human lung giant cell carcinoma LU65C cells to electrophoretically homogeneous form through five sequential purification steps: DEAE-Sepharose, CM-Sepharose, HPLC on carboxyl-methylated-polyvinylalcohol resin, hydrophobic, and reversed-phase. carboxyl-methylated-polyvinylalcohol 303-339 C-X-C motif chemokine ligand 8 Homo sapiens 56-89 2659722-1 1989 A chemotactic protein for polymorphonuclear leukocytes (lung carcinoma-derived chemotaxin [LUCT]) was purified from culture fluid of the human lung giant cell carcinoma LU65C cells to electrophoretically homogeneous form through five sequential purification steps: DEAE-Sepharose, CM-Sepharose, HPLC on carboxyl-methylated-polyvinylalcohol resin, hydrophobic, and reversed-phase. carboxyl-methylated-polyvinylalcohol 303-339 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 9948930-0 1989 Molecular-dynamics simulation of positive-ion and neutral halogen desorption following Na K-shell Auger cascades in the NaF crystal. Halogens 58-65 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 2666307-3 1989 When combined with prostaglandin E2(PGE2), MONAP caused a marked and synergistic increase in PMNL infiltration and plasma extravasation into the injected skin sites. Dinoprostone 19-35 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 2666307-3 1989 When combined with prostaglandin E2(PGE2), MONAP caused a marked and synergistic increase in PMNL infiltration and plasma extravasation into the injected skin sites. Dinoprostone 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 2523801-3 1989 Although GCP/IL-8 and beta-thromboglobulin had a similar affinity for heparin, they could be separated on a cation-exchange column. Heparin 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 2732364-4 1989 Addition of NaF solution to aluminium- and calcium-containing abrasives resulted in losses of 60-90 per cent of the added F after 1 week"s storage at room temperature. Aluminum 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 2732364-4 1989 Addition of NaF solution to aluminium- and calcium-containing abrasives resulted in losses of 60-90 per cent of the added F after 1 week"s storage at room temperature. Calcium 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 2732364-7 1989 Silica was inert in binding and inactivating F of NaF and Na2PO3F (MFP). Silicon Dioxide 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 2732364-8 1989 Calcium-containing abrasives were markedly more compatible with MFP than with NaF. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 2500593-12 1989 The types of aberrations, mostly deletions and gaps, the induction of endoreduplicated cells, the cell-cycle delay and the sensitivity of G2 cells to NaF observed are similar to that reported in the literature for DNA synthesis/repair inhibitors like aphidicolin (APC). Aphidicolin 251-262 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 2664463-5 1989 Actinomycin D chase experiments yielded evidence that cytoplasmic stabilization was one of the means of regulation of MONAP expression. Dactinomycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 2557868-0 1989 Fluoride uptake from NaF/pyrophosphate anticalculus dentifrices in vitro: effect of pyrophosphate dose. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 2484420-3 1989 Using laser microprobe mass analysis, the localization of lead and fluoride was studied in the different layers or tooth germs that had been cultured in a medium to which PbCl2 of NaF had been added in different concentrations. lead chloride 171-176 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 2648385-6 1989 Thus, GDCF and MDNCF have a similar gross secondary structure because of the loops formed by the clustered disulfides, and their different leukocyte specificities are most likely determined by the large differences in primary sequence. Disulfides 107-117 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 2918134-1 1989 Previous work showed that plaque fluoride increased with increasing NaF content of mouthwashes following daily use. Fluorides 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 2918136-1 1989 Submandibular/sublingual saliva and blood were collected from five subjects after ingestion of 1 mg fluoride as NaF. Fluorides 100-108 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 2647892-4 1989 Based on the SDS-PAGE analysis of chemically crosslinked 125I-MDNCF receptor complex, there are two polypeptides that bind MDNCF; the molecular weight of these two MDNCF receptors were estimated to be 67,000 and 59,000. Sodium Dodecyl Sulfate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 2647892-4 1989 Based on the SDS-PAGE analysis of chemically crosslinked 125I-MDNCF receptor complex, there are two polypeptides that bind MDNCF; the molecular weight of these two MDNCF receptors were estimated to be 67,000 and 59,000. Sodium Dodecyl Sulfate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 2647892-4 1989 Based on the SDS-PAGE analysis of chemically crosslinked 125I-MDNCF receptor complex, there are two polypeptides that bind MDNCF; the molecular weight of these two MDNCF receptors were estimated to be 67,000 and 59,000. Sodium Dodecyl Sulfate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 2566599-3 1989 The chemical shifts, which are referenced to 20 mM NaF in 50 mM sodium phosphate, pH 7.0, were 6.0, 8.2, and 11.9 ppm for free o-, m-, and p-fluorobenzoates, respectively, while those of o-, m-, and p-fluorobenzoates bound to DAO were 12.5, 5.4, and 13.1 ppm, respectively. sodium phosphate 64-80 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 2566599-3 1989 The chemical shifts, which are referenced to 20 mM NaF in 50 mM sodium phosphate, pH 7.0, were 6.0, 8.2, and 11.9 ppm for free o-, m-, and p-fluorobenzoates, respectively, while those of o-, m-, and p-fluorobenzoates bound to DAO were 12.5, 5.4, and 13.1 ppm, respectively. fluorobenzoates 141-156 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 2566599-3 1989 The chemical shifts, which are referenced to 20 mM NaF in 50 mM sodium phosphate, pH 7.0, were 6.0, 8.2, and 11.9 ppm for free o-, m-, and p-fluorobenzoates, respectively, while those of o-, m-, and p-fluorobenzoates bound to DAO were 12.5, 5.4, and 13.1 ppm, respectively. , and p-fluorobenzoates 133-156 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 2736581-5 1989 The results show that F absorption from MFP in milk is as high as that of NaF in water under fasting conditions and that the F bioavailability decrease from NaF in water is more important than that of MFP in milk when F ingestion occurs simultaneously with food intake. Water 81-86 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 2790854-1 1989 Specimens of human dental enamel were topically applied with solutions of sodium fluoride (NaF) or acidulated phosphate fluoride (APF) before and after laser irradiation. Sodium Fluoride 74-89 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 2790854-5 1989 NaF application caused lesser acid resistance and lesser fluoride uptake than APF application, even when the enamel was treated with laser irradiation. Fluorides 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2790857-2 1989 The saliva was collected continuously for 120 min after ingestion of 1 mg fluoride as NaF. Fluorides 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 2561943-2 1989 LiCl, BeCl2 and NaF inhibited the hydrolysis of both monophosphates with half maximal inhibition occurring at 1.2 mM, 0.3 microM, 0.25 mM (Ins 1P) and 0.14 mM, 0.56 microM, 0.28 mM (Ins 4P) respectively. monophosphates 53-67 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 2736581-5 1989 The results show that F absorption from MFP in milk is as high as that of NaF in water under fasting conditions and that the F bioavailability decrease from NaF in water is more important than that of MFP in milk when F ingestion occurs simultaneously with food intake. Water 164-169 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 2910959-0 1989 Influence of milk and food on fluoride bioavailability from NaF and Na2FPO3 in man. Fluorides 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 2714300-3 1989 The uptake of 67Ga into tumor cells was inhibited by adding NaF which is an inhibitor of ATP production. Adenosine Triphosphate 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 2648135-1 1989 Human monocyte-derived neutrophil chemotactic factor (MDNCF) was purified from culture supernatant of lipopolysaccharide-stimulated human peripheral blood mononuclear leukocytes on a column of Sepharose-bound murine monoclonal anti-MDNCF. Sepharose 193-202 C-X-C motif chemokine ligand 8 Homo sapiens 6-52 2642504-7 1989 beta-ENAP shows biochemical and biologic similarities to monocyte- and lymphocyte-derived neutrophil-activating peptides MONAP and LYNAP, which recently were purified and sequenced. (2-benzoylethyl)trimethylammonium 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 131-136 2642504-7 1989 beta-ENAP shows biochemical and biologic similarities to monocyte- and lymphocyte-derived neutrophil-activating peptides MONAP and LYNAP, which recently were purified and sequenced. Enalapril maleate 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 131-136 2648135-1 1989 Human monocyte-derived neutrophil chemotactic factor (MDNCF) was purified from culture supernatant of lipopolysaccharide-stimulated human peripheral blood mononuclear leukocytes on a column of Sepharose-bound murine monoclonal anti-MDNCF. Sepharose 193-202 C-X-C motif chemokine ligand 8 Homo sapiens 54-59 2689542-8 1989 CaF2 production amounts were relatively higher in a group of one time 2% NaF application with the use of F-ion than those of control group as only fluoride solution applicated and it were the most in a group of 10 times fluoride application with the use of F-ion, through the examining by X-ray diffractometer, so it was estimated that F-ion technique of fluoride application would increase the fluoride penetration effect. Fluorides 147-155 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 2850702-3 1988 The results showed that the CaF2-like material deposited on enamel after a topical treatment with 2% NaF dissolved almost completely in the 1 M HClO4 and 1.6 N HCl/70% glycerol solutions. Perchloric Acid 144-149 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 2848025-5 1988 Incubation of the cells with NaF also induced mobilization of the same Ca2+ stores released in response to extracellular ATP; this provided indirect evidence that the transmembrane signaling actions of P2-purinergic receptors may be mediated by GTP-binding regulatory proteins. Adenosine Triphosphate 121-124 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 2850702-3 1988 The results showed that the CaF2-like material deposited on enamel after a topical treatment with 2% NaF dissolved almost completely in the 1 M HClO4 and 1.6 N HCl/70% glycerol solutions. Hydrochloric Acid 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 2848025-5 1988 Incubation of the cells with NaF also induced mobilization of the same Ca2+ stores released in response to extracellular ATP; this provided indirect evidence that the transmembrane signaling actions of P2-purinergic receptors may be mediated by GTP-binding regulatory proteins. Guanosine Triphosphate 245-248 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 3057503-5 1988 Recombinant NAF purified to homogeneity had identical amino- and carboxyl-terminal sequences to the 72-amino acid natural NAF. 72-amino acid 100-113 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 2904148-3 1988 The identical pattern of inhibition of F1-type ATPase activity obtained in the presence of ADP and NaF with beryllium, a metal that forms fluoride complexes strictly tetracoordinated, suggests that aluminum acts through a tetrahedral complex. Beryllium 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 3213443-5 1988 Calcium fluoride-like material, formed on enamel by treatment with 2% NaF solution, was shown by scanning electron microscopy to have higher stability in saliva than in water after 3 weeks" incubation. Calcium Fluoride 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 3213443-5 1988 Calcium fluoride-like material, formed on enamel by treatment with 2% NaF solution, was shown by scanning electron microscopy to have higher stability in saliva than in water after 3 weeks" incubation. Water 169-174 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 2904148-3 1988 The identical pattern of inhibition of F1-type ATPase activity obtained in the presence of ADP and NaF with beryllium, a metal that forms fluoride complexes strictly tetracoordinated, suggests that aluminum acts through a tetrahedral complex. Metals 121-126 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 3057503-5 1988 Recombinant NAF purified to homogeneity had identical amino- and carboxyl-terminal sequences to the 72-amino acid natural NAF. 72-amino acid 100-113 C-X-C motif chemokine ligand 8 Homo sapiens 122-125 2904148-3 1988 The identical pattern of inhibition of F1-type ATPase activity obtained in the presence of ADP and NaF with beryllium, a metal that forms fluoride complexes strictly tetracoordinated, suggests that aluminum acts through a tetrahedral complex. Fluorides 138-146 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 3044830-3 1988 MDNCF forms two loops via a neighboring pair of disulfide bridges, the probable locations of which are residues 7-34 and 9-50. Disulfides 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 2904148-3 1988 The identical pattern of inhibition of F1-type ATPase activity obtained in the presence of ADP and NaF with beryllium, a metal that forms fluoride complexes strictly tetracoordinated, suggests that aluminum acts through a tetrahedral complex. Aluminum 198-206 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 3211715-7 1988 NaF (5 mmol/l) increased [Cai2+] to 412 +/- 88 nmol/l in control cells and was equally effective in cells desensitized to bradykinin. cai2+ 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2846571-3 1988 Adenylate cyclase can be stimulated by vanadate, which, like NaF, probably acts through Gs. Vanadates 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 9945944-0 1988 Electronic structure and optical properties of the impurity Cu+ in NaF. Copper 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 3165239-7 1988 Daily fluoride mouth rinsing with a 0.2% solution sodium fluoride (NaF) retarded lesion development significantly, whereas the fluoride solution with low pH inhibited lesion formation completely. Fluorides 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 3165239-7 1988 Daily fluoride mouth rinsing with a 0.2% solution sodium fluoride (NaF) retarded lesion development significantly, whereas the fluoride solution with low pH inhibited lesion formation completely. Sodium Fluoride 50-65 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 3165239-7 1988 Daily fluoride mouth rinsing with a 0.2% solution sodium fluoride (NaF) retarded lesion development significantly, whereas the fluoride solution with low pH inhibited lesion formation completely. Fluorides 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 3260265-3 1988 Comparison of the deduced amino acid sequence with the NH2-terminal amino acid sequence of natural MDNCF shows that the mature functional protein comprises 72 amino acids, beginning with serine at residue 28. Serine 187-193 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 3214557-0 1988 In situ fluoride uptake from NaF dentifrices: dose response and effects of a novel enhanced delivery system. Fluorides 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 3214558-0 1988 In situ fluoride uptake from 0.05% neutral NaF mouthrinses: effects of a novel enhanced delivery system. Fluorides 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 2845938-9 1988 AlF4- probably binds to the phosphate-binding site of the ATPase, as the Ki for inhibition of the (Na+ + K+)-ATPase and of the plasmalemmal (Ca2+ + Mg2+)-ATPase is shifted in the presence of respectively 5 and 50 mM-Pi to higher concentrations of NaF. Phosphates 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 247-250 2840318-5 1988 Two conclusions are drawn from these results: 1) neutrophil activation by NAF (as by fMLP) is dependent on a GTP-binding protein and on protein kinase C; 2) a similar, or even identical, mechanism of signal transduction must be assumed on stimulation of human neutrophils with NAF, fMLP, and other chemotactic agonists. Guanosine Triphosphate 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 3282512-3 1988 Analytic isoelecto-focusing of pure MONAP (single line upon sodiumdodecylsulfate polyacrylamide gel electrophoresis, single peak after RP-18-HPLC), obtained by size exclusion HPLC followed by two different reversed phase HPLC steps revealed charge heterogeneity giving major components with isoelectric points at 4.7, 4.9, 6.4 and 6.9, all of which exhibited chemotactic activity. Sodium Dodecyl Sulfate 60-80 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 3283118-5 1988 Ins-1,4,5-P3 formation was also increased by NaF, further indicating the involvement of a guanine nucleotide regulatory protein. Inositol 1,4,5-Trisphosphate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 3283239-5 1988 LYNAP stimulated neutrophil chemotaxis (ED50 of 3 +/- 3 ng/ml), chemokinesis (ED50 of 2 +/- 2 ng/ml), and caused degranulation of cytochalasin B pretreated human neutrophils (ED50 of 20 ng/ml). Cytochalasin B 130-144 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 3282512-3 1988 Analytic isoelecto-focusing of pure MONAP (single line upon sodiumdodecylsulfate polyacrylamide gel electrophoresis, single peak after RP-18-HPLC), obtained by size exclusion HPLC followed by two different reversed phase HPLC steps revealed charge heterogeneity giving major components with isoelectric points at 4.7, 4.9, 6.4 and 6.9, all of which exhibited chemotactic activity. polyacrylamide 81-95 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 2833319-2 1988 In both groups, significant inverse correlations were observed when 24-hr urinary catecholamine levels were examined in relation to measures of both receptor-mediated (prostaglandin D2 and alpha 2-adrenergic) and postreceptor-mediated (NaF) platelet AC enzyme activities, suggesting that circulating catecholamines may regulate platelet AC by heterologous (agonist-nonspecific) desensitization of the AC enzyme complex. Catecholamines 82-95 C-X-C motif chemokine ligand 8 Homo sapiens 236-239 3271662-0 1988 [Trials of increasing the ability of enamel enrichment with fluorine by adding NaF and Na2PO3F to toothpastes. Fluorine 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 3366793-1 1988 Con A, NaF, and eserine (lysosomotropic agents) induced marked translocation of acidic [3H] nonhistone proteins (NHP) from the cytoplasm to the nucleus in lymphocytes prelabeled with [3H]-2-mannose. Tritium 88-90 C-X-C motif chemokine ligand 8 Homo sapiens 7-10 3366793-1 1988 Con A, NaF, and eserine (lysosomotropic agents) induced marked translocation of acidic [3H] nonhistone proteins (NHP) from the cytoplasm to the nucleus in lymphocytes prelabeled with [3H]-2-mannose. Tritium 184-186 C-X-C motif chemokine ligand 8 Homo sapiens 7-10 3366793-1 1988 Con A, NaF, and eserine (lysosomotropic agents) induced marked translocation of acidic [3H] nonhistone proteins (NHP) from the cytoplasm to the nucleus in lymphocytes prelabeled with [3H]-2-mannose. 2-mannose 188-197 C-X-C motif chemokine ligand 8 Homo sapiens 7-10 3366793-5 1988 Con A and NaF caused also nuclear translocation of acidic [3H] NHP in cells labeled with [3H] glucosamine, [3H] galactose, or [3H] fucose. Tritium 59-61 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 3366793-5 1988 Con A and NaF caused also nuclear translocation of acidic [3H] NHP in cells labeled with [3H] glucosamine, [3H] galactose, or [3H] fucose. [3h] glucosamine 89-105 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 3366793-5 1988 Con A and NaF caused also nuclear translocation of acidic [3H] NHP in cells labeled with [3H] glucosamine, [3H] galactose, or [3H] fucose. 3h] galactose 108-121 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 3366793-5 1988 Con A and NaF caused also nuclear translocation of acidic [3H] NHP in cells labeled with [3H] glucosamine, [3H] galactose, or [3H] fucose. Tritium 90-92 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 3366793-5 1988 Con A and NaF caused also nuclear translocation of acidic [3H] NHP in cells labeled with [3H] glucosamine, [3H] galactose, or [3H] fucose. Fucose 131-137 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 3248408-0 1988 [Fluorine content of the superficial enamel layer after application in vitro of pastes with varying concentrations of Na2PO3F or NaF]. Fluorine 1-9 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 3123517-11 1988 Lactate, the principal product of resting neutrophil glucose catabolism, was demonstrable in cell-free supernatants after incubation at 37 degrees C. Lactate accumulation was inhibited by NaF and decreased temperature of incubation. Lactic Acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 188-191 2452749-7 1988 The diminished response of the enzyme to GTP and NaF pointed to an involvement of the stimulatory guanyl nucleotide-binding protein (Gs) in iloprost-induced heterologous desensitization. Iloprost 140-148 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 3348776-1 1988 The ability of sodium fluoride (NaF) and thrombin to stimulate aggregation and protein phosphorylation in intact human platelets was measured and compared. Sodium Fluoride 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 3348776-5 1988 Phosphoamino acid analysis showed that the phosphorylated amino acids of the 47 KDa protein from platelets activated by NaF and thrombin were slightly different. Phosphoamino Acids 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 3123517-11 1988 Lactate, the principal product of resting neutrophil glucose catabolism, was demonstrable in cell-free supernatants after incubation at 37 degrees C. Lactate accumulation was inhibited by NaF and decreased temperature of incubation. Lactic Acid 150-157 C-X-C motif chemokine ligand 8 Homo sapiens 188-191 3126375-1 1988 The sensitivity of fibroblasts (L cells) to low concentrations of sodium fluoride (NaF) was examined using the same cell during a series of stimuli. Sodium Fluoride 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 2838616-4 1988 0.2-0.3 mM fatty acids increased adenylate cyclase activity, while higher concentrations of arachidonic and linoleic acids, but not oleic acid, inhibited basal, beta-agonist- and NaF-stimulated activities in membranes of A431 and C6 cells. Fatty Acids 11-22 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 2838616-4 1988 0.2-0.3 mM fatty acids increased adenylate cyclase activity, while higher concentrations of arachidonic and linoleic acids, but not oleic acid, inhibited basal, beta-agonist- and NaF-stimulated activities in membranes of A431 and C6 cells. arachidonic 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 2838616-4 1988 0.2-0.3 mM fatty acids increased adenylate cyclase activity, while higher concentrations of arachidonic and linoleic acids, but not oleic acid, inhibited basal, beta-agonist- and NaF-stimulated activities in membranes of A431 and C6 cells. Linoleic Acids 108-122 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 2838616-4 1988 0.2-0.3 mM fatty acids increased adenylate cyclase activity, while higher concentrations of arachidonic and linoleic acids, but not oleic acid, inhibited basal, beta-agonist- and NaF-stimulated activities in membranes of A431 and C6 cells. Oleic Acid 111-121 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 2824608-1 1987 A novel monocyte-derived neutrophil-activating peptide (MONAP) produced by lipopolysaccharide- and phorbol myristate acetate-stimulated human peripheral blood monocytes was purified by sequential ion exchange-high performance liquid chromatography (HPLC), size exclusion HPLC, and reversed phase HPLC. Tetradecanoylphorbol Acetate 99-124 C-X-C motif chemokine ligand 8 Homo sapiens 8-54 2826233-1 1987 The free modulator subunit of the ATP,Mg-dependent phosphatase is phosphorylated up to 1 mol per mol by casein kinase-1, up to 1.85 mol per mol after dephosphorylation by the PCSH1 phosphatase, but 10-fold less when purified in the presence of NaF, suggesting an in vivo phosphorylation of the casein kinase-1 sites. Adenosine Triphosphate 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 244-247 2839752-4 1988 In the presence of AlCl3 NaF stimulated the release of inositol phosphates in the cytotoxin-treated JURKAT cells. Inositol Phosphates 55-74 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 2839752-5 1988 NaF plus AlCl3 induced increases in inositol tris-, bis-, and mono-phosphates and decreases in PtdIns(4,5)P2, phosphatidylinositol 4-phosphate, and phosphatidylinositol within 5 min after addition to the cytotoxin-treated cells at 37 C. GTP gamma S stimulated, to some extent, polyphosphoinositide hydrolysis in the cytotoxin-treated JURKAT. inositol tris-, bis-, and mono-phosphates 36-77 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2839752-5 1988 NaF plus AlCl3 induced increases in inositol tris-, bis-, and mono-phosphates and decreases in PtdIns(4,5)P2, phosphatidylinositol 4-phosphate, and phosphatidylinositol within 5 min after addition to the cytotoxin-treated cells at 37 C. GTP gamma S stimulated, to some extent, polyphosphoinositide hydrolysis in the cytotoxin-treated JURKAT. Phosphatidylinositol 4,5-Diphosphate 95-108 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2839752-5 1988 NaF plus AlCl3 induced increases in inositol tris-, bis-, and mono-phosphates and decreases in PtdIns(4,5)P2, phosphatidylinositol 4-phosphate, and phosphatidylinositol within 5 min after addition to the cytotoxin-treated cells at 37 C. GTP gamma S stimulated, to some extent, polyphosphoinositide hydrolysis in the cytotoxin-treated JURKAT. phosphatidylinositol 4-phosphate 110-142 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2839752-5 1988 NaF plus AlCl3 induced increases in inositol tris-, bis-, and mono-phosphates and decreases in PtdIns(4,5)P2, phosphatidylinositol 4-phosphate, and phosphatidylinositol within 5 min after addition to the cytotoxin-treated cells at 37 C. GTP gamma S stimulated, to some extent, polyphosphoinositide hydrolysis in the cytotoxin-treated JURKAT. Phosphatidylinositols 110-130 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2839752-5 1988 NaF plus AlCl3 induced increases in inositol tris-, bis-, and mono-phosphates and decreases in PtdIns(4,5)P2, phosphatidylinositol 4-phosphate, and phosphatidylinositol within 5 min after addition to the cytotoxin-treated cells at 37 C. GTP gamma S stimulated, to some extent, polyphosphoinositide hydrolysis in the cytotoxin-treated JURKAT. Guanosine Triphosphate 237-240 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2839752-5 1988 NaF plus AlCl3 induced increases in inositol tris-, bis-, and mono-phosphates and decreases in PtdIns(4,5)P2, phosphatidylinositol 4-phosphate, and phosphatidylinositol within 5 min after addition to the cytotoxin-treated cells at 37 C. GTP gamma S stimulated, to some extent, polyphosphoinositide hydrolysis in the cytotoxin-treated JURKAT. Phosphatidylinositol Phosphates 277-297 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3322281-4 1987 Crude and pure NAF stimulated human neutrophils to release granule enzymes and to produce superoxide and H2O2. Superoxides 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 3322281-4 1987 Crude and pure NAF stimulated human neutrophils to release granule enzymes and to produce superoxide and H2O2. Hydrogen Peroxide 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 2824608-1 1987 A novel monocyte-derived neutrophil-activating peptide (MONAP) produced by lipopolysaccharide- and phorbol myristate acetate-stimulated human peripheral blood monocytes was purified by sequential ion exchange-high performance liquid chromatography (HPLC), size exclusion HPLC, and reversed phase HPLC. Tetradecanoylphorbol Acetate 99-124 C-X-C motif chemokine ligand 8 Homo sapiens 56-61 2824608-3 1987 Purified MONAP was found to be homogeneous, giving a single peak on size-exclusion HPLC, reversed-phase HPLC, as well as a single 10-kDa band on silver-stained polyacrylamide gels. polyacrylamide 160-174 C-X-C motif chemokine ligand 8 Homo sapiens 9-14 2824608-4 1987 Purified MONAP stimulate human neutrophil chemotaxis at an estimated molarity of 5 x 10(-11) M. Half-maximal enzyme release of cytochalasin B pretreated neutrophils occurred at 2 to 3 x 10(-10) M, whereas superoxide anion production elicited by various concentrations of MONAP was found to be low. Cytochalasin B 127-141 C-X-C motif chemokine ligand 8 Homo sapiens 9-14 2824608-4 1987 Purified MONAP stimulate human neutrophil chemotaxis at an estimated molarity of 5 x 10(-11) M. Half-maximal enzyme release of cytochalasin B pretreated neutrophils occurred at 2 to 3 x 10(-10) M, whereas superoxide anion production elicited by various concentrations of MONAP was found to be low. Cytochalasin B 127-141 C-X-C motif chemokine ligand 8 Homo sapiens 271-276 3120720-4 1987 Moreover, the dose-response effects of NaF on arachidonate release and DG formation were different. Arachidonic Acid 46-58 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 2824608-4 1987 Purified MONAP stimulate human neutrophil chemotaxis at an estimated molarity of 5 x 10(-11) M. Half-maximal enzyme release of cytochalasin B pretreated neutrophils occurred at 2 to 3 x 10(-10) M, whereas superoxide anion production elicited by various concentrations of MONAP was found to be low. Superoxides 205-221 C-X-C motif chemokine ligand 8 Homo sapiens 9-14 3429387-3 1987 Elimination of O2-dependent antimicrobial systems with retention of phagocytic activity was achieved by using polymorphs from children with chronic granulomatous disease NaF-pulsed normal polymorphs. Oxygen 15-17 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 2825101-6 1987 In addition, the corticosteroidogenic effect of forskolin and NaF (which respectively stimulate the adenylate-cyclase subunit and the guanyl nucleotide regularly protein) was not affected by vinblastine. guanyl nucleotide 134-151 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 10872408-1 1987 The purpose of this investigation was to examine the potential genotoxic influence of sodium fluoride (NaF) on mammalian cells by means of a mouse bone-marrow micronucleus test. Sodium Fluoride 86-101 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 10872408-8 1987 The results indicated that doses of NaF up to the MTD did not significantly increase the frequencies of MN-PCE when compared with the negative controls, although the bone fluoride content increased as the dose of NaF was increased. Fluorides 171-179 C-X-C motif chemokine ligand 8 Homo sapiens 213-216 2825667-2 1987 NAF also induced the generation of 5(S),12(R)-dihydroxy-6,14-cis-8,10-trans-eicosatetraenoic acid [Leukotriene B4 (LTB4)] by PMNs which was enhanced in the presence of exogenous arachidonic acid (AA). 5(s),12(r)-dihydroxy-6,14-cis-8,10-trans-eicosatetraenoic acid 35-97 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2825667-2 1987 NAF also induced the generation of 5(S),12(R)-dihydroxy-6,14-cis-8,10-trans-eicosatetraenoic acid [Leukotriene B4 (LTB4)] by PMNs which was enhanced in the presence of exogenous arachidonic acid (AA). Leukotriene B4 99-113 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2825667-2 1987 NAF also induced the generation of 5(S),12(R)-dihydroxy-6,14-cis-8,10-trans-eicosatetraenoic acid [Leukotriene B4 (LTB4)] by PMNs which was enhanced in the presence of exogenous arachidonic acid (AA). Leukotriene B4 115-119 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2825667-2 1987 NAF also induced the generation of 5(S),12(R)-dihydroxy-6,14-cis-8,10-trans-eicosatetraenoic acid [Leukotriene B4 (LTB4)] by PMNs which was enhanced in the presence of exogenous arachidonic acid (AA). Arachidonic Acid 178-194 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2825667-4 1987 15(S)-hydroxy-5,8,11-cis-13-trans-eicosatetraenoic acid (15-HETE), a product of the 15-lipoxy-genation of AA in PMNS, caused a concentration-dependent suppression of degranulation and LTB4 generation by PMNs in contact with NAF. 15(s)-hydroxy-5,8,11-cis-13-trans-eicosatetraenoic acid 0-55 C-X-C motif chemokine ligand 8 Homo sapiens 224-227 2825667-4 1987 15(S)-hydroxy-5,8,11-cis-13-trans-eicosatetraenoic acid (15-HETE), a product of the 15-lipoxy-genation of AA in PMNS, caused a concentration-dependent suppression of degranulation and LTB4 generation by PMNs in contact with NAF. 15-Hete 57-64 C-X-C motif chemokine ligand 8 Homo sapiens 224-227 2825667-5 1987 15-HETE also inhibited the rise in cytosolic-free calcium [( Ca2+]i) observed in NAF activated PMNs. 15-Hete 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 2825667-5 1987 15-HETE also inhibited the rise in cytosolic-free calcium [( Ca2+]i) observed in NAF activated PMNs. Calcium 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 3114629-3 1987 Sodium fluoride (NaF) has previously been shown to be clastogenic in vitro in Syrian hamster cells and human fibroblasts. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 3114629-8 1987 (2) NaCl is weakly clastogenic at 1000 times the threshold dose for NaF. Sodium Chloride 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 3038870-7 1987 The same holds true for NaF and guanosine 5"-(beta, gamma-imido)trisphosphate, indicating a constant activity of the guanine nucleotide regulatory unit which mediates hormonal stimulation of adenylate cyclase (Ns). Guanine Nucleotides 117-135 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 3657146-1 1987 Desmethylnafoxidine aziridine (Naf-Az), an affinity label for the estrogen receptor based structurally on the antiestrogen nafoxidine, has been prepared in unlabeled and in high specific activity, tritium-labeled form and has been evaluated for its apparent competitive binding, and time-dependent irreversible, covalent attachment to the estrogen receptor. desmethylnafoxidine aziridine 0-29 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 3657146-1 1987 Desmethylnafoxidine aziridine (Naf-Az), an affinity label for the estrogen receptor based structurally on the antiestrogen nafoxidine, has been prepared in unlabeled and in high specific activity, tritium-labeled form and has been evaluated for its apparent competitive binding, and time-dependent irreversible, covalent attachment to the estrogen receptor. Nafoxidine 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 3657146-1 1987 Desmethylnafoxidine aziridine (Naf-Az), an affinity label for the estrogen receptor based structurally on the antiestrogen nafoxidine, has been prepared in unlabeled and in high specific activity, tritium-labeled form and has been evaluated for its apparent competitive binding, and time-dependent irreversible, covalent attachment to the estrogen receptor. Tritium 197-204 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 3657146-2 1987 Naf-Az was synthesized through a key 1,2-diaryl-3,4-dihydronaphthalene intermediate that was prepared from 6-methoxy-1-tetralone by two routes involving alternate strategies for arylation. 1,2-diaryl-3,4-dihydronaphthalene 37-70 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3657146-2 1987 Naf-Az was synthesized through a key 1,2-diaryl-3,4-dihydronaphthalene intermediate that was prepared from 6-methoxy-1-tetralone by two routes involving alternate strategies for arylation. 6-Methoxy-1-tetralone 107-128 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3657146-3 1987 Conversion of the diaryldihydronaphthalene to Naf-Az through a series of deprotection-activation reactions culminated in ethyleneimine displacement of a methanesulfonate. diaryldihydronaphthalene 18-42 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 3657146-3 1987 Conversion of the diaryldihydronaphthalene to Naf-Az through a series of deprotection-activation reactions culminated in ethyleneimine displacement of a methanesulfonate. aziridine 121-134 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 3657146-3 1987 Conversion of the diaryldihydronaphthalene to Naf-Az through a series of deprotection-activation reactions culminated in ethyleneimine displacement of a methanesulfonate. methanesulfonic acid 153-169 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 3657146-5 1987 Compared to our previously-prepared reagent tamoxifen aziridine (Tam-Az), Naf-Az has a higher apparent competitive binding affinity, and it reacts with the estrogen receptor in cytosol preparations and in intact MCF-7 breast cancer cells rapidly and with at least comparable efficiency and selectivity. Tamoxifen 44-53 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 3657146-5 1987 Compared to our previously-prepared reagent tamoxifen aziridine (Tam-Az), Naf-Az has a higher apparent competitive binding affinity, and it reacts with the estrogen receptor in cytosol preparations and in intact MCF-7 breast cancer cells rapidly and with at least comparable efficiency and selectivity. aziridine 54-63 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 3657146-5 1987 Compared to our previously-prepared reagent tamoxifen aziridine (Tam-Az), Naf-Az has a higher apparent competitive binding affinity, and it reacts with the estrogen receptor in cytosol preparations and in intact MCF-7 breast cancer cells rapidly and with at least comparable efficiency and selectivity. tamoxifen aziridine 65-71 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 3028538-2 1987 At lower concentrations, with a peak activity between 30 and 40 mmol/L, NaF induced aggregation and release of adenosine 5"-triphosphate (ATP) that was associated with increased formation of inositol phosphates, a rise in cytosolic free Ca2+, and phosphorylation of 20-kd and 40-kd proteins. Adenosine Triphosphate 111-136 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 3111669-1 1987 Daily treatment with 30 mg of sodium fluoride (NaF) and 1 g of calcium over a 3-year period increased the bone mineral content (BMC) in the spines of women (n = 25) with osteoporosis. Sodium Fluoride 30-45 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 2882783-3 1987 Human but not bovine serum albumin in the presence of NaF abolished activation of heme-containing guanylate cyclase by NO and nitroso compounds, whereas enzyme activation by arachidonic acid was markedly enhanced. Nitroso Compounds 126-143 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 2885225-2 1987 The formation of inositol bis- and trisphosphates was stimulated in a buffer with 110 nM free Ca2+ with a nonhydrolyzable GTP analogue, GTP gamma S, and NaF plus AlCl3 in a time- and concentration-dependent manner. inositol bis- and trisphosphates 17-49 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 2885225-4 1987 AlCl3 enhanced the NaF-stimulated release of inositol polyphosphates. Aluminum Chloride 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 2885225-4 1987 AlCl3 enhanced the NaF-stimulated release of inositol polyphosphates. inositol polyphosphates 45-68 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 2885225-5 1987 Optimum concentrations of NaF and AlCl3 produced 1.5-fold more inositol polyphosphates than that produced by optimum concentration of GTP gamma S. OKT3 monoclonal antibody, an antibody against the T-cell receptor complex, did not stimulate the inositol polyphosphate formation by JURKAT membranes even in the presence of GTP, although the antibody at the concentrations used markedly stimulated the hydrolysis of polyphosphoinositides in intact JURKAT cells. inositol polyphosphates 63-86 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 2885225-5 1987 Optimum concentrations of NaF and AlCl3 produced 1.5-fold more inositol polyphosphates than that produced by optimum concentration of GTP gamma S. OKT3 monoclonal antibody, an antibody against the T-cell receptor complex, did not stimulate the inositol polyphosphate formation by JURKAT membranes even in the presence of GTP, although the antibody at the concentrations used markedly stimulated the hydrolysis of polyphosphoinositides in intact JURKAT cells. Phytic Acid 63-85 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 2885225-5 1987 Optimum concentrations of NaF and AlCl3 produced 1.5-fold more inositol polyphosphates than that produced by optimum concentration of GTP gamma S. OKT3 monoclonal antibody, an antibody against the T-cell receptor complex, did not stimulate the inositol polyphosphate formation by JURKAT membranes even in the presence of GTP, although the antibody at the concentrations used markedly stimulated the hydrolysis of polyphosphoinositides in intact JURKAT cells. Guanosine Triphosphate 321-324 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 2885225-5 1987 Optimum concentrations of NaF and AlCl3 produced 1.5-fold more inositol polyphosphates than that produced by optimum concentration of GTP gamma S. OKT3 monoclonal antibody, an antibody against the T-cell receptor complex, did not stimulate the inositol polyphosphate formation by JURKAT membranes even in the presence of GTP, although the antibody at the concentrations used markedly stimulated the hydrolysis of polyphosphoinositides in intact JURKAT cells. Phosphatidylinositol Phosphates 413-434 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 3032933-3 1987 PtdIns-P2 phospholipase C was also activated by nucleoside triphosphates, citrate, EDTA, and NaF. Phosphatidylinositol 4,5-Diphosphate 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 3028538-2 1987 At lower concentrations, with a peak activity between 30 and 40 mmol/L, NaF induced aggregation and release of adenosine 5"-triphosphate (ATP) that was associated with increased formation of inositol phosphates, a rise in cytosolic free Ca2+, and phosphorylation of 20-kd and 40-kd proteins. Adenosine Triphosphate 138-141 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 3028538-2 1987 At lower concentrations, with a peak activity between 30 and 40 mmol/L, NaF induced aggregation and release of adenosine 5"-triphosphate (ATP) that was associated with increased formation of inositol phosphates, a rise in cytosolic free Ca2+, and phosphorylation of 20-kd and 40-kd proteins. Inositol Phosphates 191-210 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 2436701-2 1987 Results are presented which show that prolonged incubation of platelets with iloprost (a stable prostacyclin analogue) results in a reduction in the capacity for adenylate cyclase activation by the adenosine analogue 5"-(N-ethyl)-carboxamidoadenosine (NECA), NaF, guanyl-5"-yl imidodiphosphate or GTP. Epoprostenol 96-108 C-X-C motif chemokine ligand 8 Homo sapiens 259-262 3028538-3 1987 At NaF concentrations greater than 40 mmol/L, aggregation and ATP release decreased dose-dependently in parallel with a decrease in Ca2+ mobilization, whereas neither inositol phosphate formation nor 40-kd protein phosphorylation was reduced. Adenosine Triphosphate 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 3-6 3028538-4 1987 At these concentrations, NaF caused a dose-dependent transient rise in platelet cyclic adenosine 3",5"-monophosphate (cAMP) levels that was sufficient to account for the observed reduction in Ca2+ mobilization, aggregation, and ATP release. Cyclic AMP 80-116 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 2436701-2 1987 Results are presented which show that prolonged incubation of platelets with iloprost (a stable prostacyclin analogue) results in a reduction in the capacity for adenylate cyclase activation by the adenosine analogue 5"-(N-ethyl)-carboxamidoadenosine (NECA), NaF, guanyl-5"-yl imidodiphosphate or GTP. Iloprost 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 259-262 3028538-4 1987 At these concentrations, NaF caused a dose-dependent transient rise in platelet cyclic adenosine 3",5"-monophosphate (cAMP) levels that was sufficient to account for the observed reduction in Ca2+ mobilization, aggregation, and ATP release. Cyclic AMP 118-122 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 3028538-4 1987 At these concentrations, NaF caused a dose-dependent transient rise in platelet cyclic adenosine 3",5"-monophosphate (cAMP) levels that was sufficient to account for the observed reduction in Ca2+ mobilization, aggregation, and ATP release. Adenosine Triphosphate 228-231 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 3028538-5 1987 Stimulated cAMP levels started declining rapidly within 30 seconds of addition of NaF, however. Cyclic AMP 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 3028538-6 1987 Similarly, prostacyclin (PGI2)-induced cAMP accumulation was temporarily enhanced but subsequently suppressed by NaF, suggesting either stimulation of a cAMP phosphodiesterase or delayed inhibition of adenylate cyclase. Epoprostenol 11-23 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 3028538-6 1987 Similarly, prostacyclin (PGI2)-induced cAMP accumulation was temporarily enhanced but subsequently suppressed by NaF, suggesting either stimulation of a cAMP phosphodiesterase or delayed inhibition of adenylate cyclase. Epoprostenol 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 3028538-7 1987 Evidence for the latter was provided by the finding that NaF pretreatment of platelets resulted in partial inhibition of PGI2-stimulated cAMP formation in the presence of the cAMP phosphodiesterase inhibitor 3-isobutyl-1-methyl-xanthine (MIX). Epoprostenol 121-125 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 3028538-7 1987 Evidence for the latter was provided by the finding that NaF pretreatment of platelets resulted in partial inhibition of PGI2-stimulated cAMP formation in the presence of the cAMP phosphodiesterase inhibitor 3-isobutyl-1-methyl-xanthine (MIX). Cyclic AMP 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 3028538-7 1987 Evidence for the latter was provided by the finding that NaF pretreatment of platelets resulted in partial inhibition of PGI2-stimulated cAMP formation in the presence of the cAMP phosphodiesterase inhibitor 3-isobutyl-1-methyl-xanthine (MIX). 1-Methyl-3-isobutylxanthine 208-236 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 3453041-7 1987 NaF, an activator of adenylate cyclase, like adrenaline, stimulated the incorporation of linoleic acid into ghost membrane phospholipids. Epinephrine 45-55 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3550448-1 1987 The mutagenicity of fluoride (as sodium fluoride, NaF) was investigated with Ames Salmonella/microsome assays in strains of TA97a, TA98, TA100, TA102 and TA1535. Fluorides 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 3453041-7 1987 NaF, an activator of adenylate cyclase, like adrenaline, stimulated the incorporation of linoleic acid into ghost membrane phospholipids. Linoleic Acid 89-102 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3453041-7 1987 NaF, an activator of adenylate cyclase, like adrenaline, stimulated the incorporation of linoleic acid into ghost membrane phospholipids. Phospholipids 123-136 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3800973-8 1986 Millimolar concentrations of NaF also stimulated the formation of inositol phosphates in membrane preparations from 1321N1 cells. Inositol Phosphates 66-85 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 3463564-3 1986 The Bmax for [3H]forskolin binding is increased to 455 and 425 fmol/mg of protein in the presence of 100 microM guanyl-5"-yl imidodiphosphate (Gpp(NH)p) and 10 mM NaF, respectively. Tritium 14-16 C-X-C motif chemokine ligand 8 Homo sapiens 163-166 3463564-3 1986 The Bmax for [3H]forskolin binding is increased to 455 and 425 fmol/mg of protein in the presence of 100 microM guanyl-5"-yl imidodiphosphate (Gpp(NH)p) and 10 mM NaF, respectively. Colforsin 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 163-166 3463564-4 1986 The increase in the Bmax for [3H]forskolin in the presence of Gpp(NH)p or NaF is not observed in the absence of MgCl2. Tritium 30-32 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 3463564-4 1986 The increase in the Bmax for [3H]forskolin in the presence of Gpp(NH)p or NaF is not observed in the absence of MgCl2. Colforsin 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 3463564-5 1986 The EC50 values for the increase in the number of binding sites for [3H]forskolin by Gpp(NH)p and NaF are 600 nM and 4 mM, respectively. Tritium 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 3463564-5 1986 The EC50 values for the increase in the number of binding sites for [3H]forskolin by Gpp(NH)p and NaF are 600 nM and 4 mM, respectively. Colforsin 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 3463564-7 1986 The increase in the number of [3H]forskolin binding sites observed in the presence of NaF is unaffected by prostaglandins. Tritium 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 3463564-7 1986 The increase in the number of [3H]forskolin binding sites observed in the presence of NaF is unaffected by prostaglandins. Colforsin 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 3435503-6 1987 Highly purified sarcolemmal membranes, exhibiting an NaF-stimulated activity of 3.46 +/- 0.65 nmol cAMP formed min-1 mg-1 of protein, were exposed to free radicals formation of which was induced by Fe++/ascorbate. Cyclic AMP 99-103 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 3435503-6 1987 Highly purified sarcolemmal membranes, exhibiting an NaF-stimulated activity of 3.46 +/- 0.65 nmol cAMP formed min-1 mg-1 of protein, were exposed to free radicals formation of which was induced by Fe++/ascorbate. Iron 198-202 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 3435503-6 1987 Highly purified sarcolemmal membranes, exhibiting an NaF-stimulated activity of 3.46 +/- 0.65 nmol cAMP formed min-1 mg-1 of protein, were exposed to free radicals formation of which was induced by Fe++/ascorbate. Ascorbic Acid 203-212 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 16665178-10 1986 When 0.3 millimolar PEP either alone or with 0.1 millimolar ATP and 0.3 millimolar NaF is present during preincubation, the effect of malate in a following assay is to activate the reaction. malic acid 134-140 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 3762571-1 1986 Sodium fluoride (NaF) was assayed for the induction of DNA-repair synthesis in WI-38 human diploid fibroblasts and in primary cultures of rat hepatocytes. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 3743666-3 1986 The lysosomotropic agents conA, NaF, eserine and atropine have two parallel effects on resting lymphocytes, after they have endocytosed [3H]NHP: inhibition of degradation and increased translocation of [3H]NHP from the cytoplasm to the nucleus. Tritium 137-139 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 3743666-3 1986 The lysosomotropic agents conA, NaF, eserine and atropine have two parallel effects on resting lymphocytes, after they have endocytosed [3H]NHP: inhibition of degradation and increased translocation of [3H]NHP from the cytoplasm to the nucleus. Tritium 203-205 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 3762571-7 1986 Published reports (Hellung-Larsen and Klenow, 1969; Srivastava et al., 1981) describe the formation of precipitable complexes of Mg2+, F-, and [3H]thymidine triphosphate which suggests that autoradiographic measurement of UDS may lead to artifacts when testing NaF unless extensive washing of the cultures is employed. magnesium ion 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 261-264 3762571-7 1986 Published reports (Hellung-Larsen and Klenow, 1969; Srivastava et al., 1981) describe the formation of precipitable complexes of Mg2+, F-, and [3H]thymidine triphosphate which suggests that autoradiographic measurement of UDS may lead to artifacts when testing NaF unless extensive washing of the cultures is employed. Tritium 144-146 C-X-C motif chemokine ligand 8 Homo sapiens 261-264 3762571-7 1986 Published reports (Hellung-Larsen and Klenow, 1969; Srivastava et al., 1981) describe the formation of precipitable complexes of Mg2+, F-, and [3H]thymidine triphosphate which suggests that autoradiographic measurement of UDS may lead to artifacts when testing NaF unless extensive washing of the cultures is employed. thymidine 5'-triphosphate 147-169 C-X-C motif chemokine ligand 8 Homo sapiens 261-264 3015678-1 1986 Partially purified plasma membranes prepared from myo-[3H]inositol-prelabeled WRK1 cells exhibit a phosphatidylinositol 4,5-biphosphate (PIP2) phospholipase C activity sensitive to NaF. myo-[3h]inositol 50-66 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 3747724-1 1986 Low, micromolar concentrations of aluminum (in the presence of NaF) were shown to strongly activate human platelet adenylate cyclase and provided a useful probe for evaluating cyclic AMP second messenger function distal to the receptor: The effect of normal aging and disease state on second messenger activity in man was studied by measurements of the aluminum-activated enzyme. Aluminum 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 3747724-1 1986 Low, micromolar concentrations of aluminum (in the presence of NaF) were shown to strongly activate human platelet adenylate cyclase and provided a useful probe for evaluating cyclic AMP second messenger function distal to the receptor: The effect of normal aging and disease state on second messenger activity in man was studied by measurements of the aluminum-activated enzyme. Cyclic AMP 176-186 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 3747724-1 1986 Low, micromolar concentrations of aluminum (in the presence of NaF) were shown to strongly activate human platelet adenylate cyclase and provided a useful probe for evaluating cyclic AMP second messenger function distal to the receptor: The effect of normal aging and disease state on second messenger activity in man was studied by measurements of the aluminum-activated enzyme. Aluminum 353-361 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 3747724-3 1986 An age-associated decline in NaF-stimulated cyclic AMP synthesis was also demonstrated for normal, non-demented subjects. Cyclic AMP 44-54 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 3015678-1 1986 Partially purified plasma membranes prepared from myo-[3H]inositol-prelabeled WRK1 cells exhibit a phosphatidylinositol 4,5-biphosphate (PIP2) phospholipase C activity sensitive to NaF. Phosphatidylinositol 4,5-Diphosphate 99-135 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 3015678-1 1986 Partially purified plasma membranes prepared from myo-[3H]inositol-prelabeled WRK1 cells exhibit a phosphatidylinositol 4,5-biphosphate (PIP2) phospholipase C activity sensitive to NaF. Phosphatidylinositol 4,5-Diphosphate 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 3015678-2 1986 NaF increased the production of IP2 and IP3 in a time- and concentration-dependent manner. Inositol 1,4,5-Trisphosphate 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3950443-3 1986 Neutralization of O2-dependent antimicrobial systems with retention of phagocytic capacity was achieved with use of PMNLs from four children with chronic granulomatous disease (CGD) or NaF-pulsed normal PMNLs. Oxygen 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 3085731-6 1986 Mitochondrial inhibitors (KCN, NaN3, antimycin A, FCCP and dinitrophenol) inhibited the potential oscillation, whereas glycolytic inhibitors (iodoacetic acid and NaF) had no effects. Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 3028102-0 1986 On the role of guanine nucleotide binding regulatory proteins (G-proteins) in signal transduction in human platelets: studies with sodium fluoride (NaF). Sodium Fluoride 131-146 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 3010521-2 1986 Gpp(NH)p and NaF are shown to be tightly bound to GTP-binding proteins (G-proteins) of outer segments of optic rods, additional activation of phosphodiesterase in the presence of Gpp(NH)p being observed after preincubation with NaF and subsequent washing of the membrane. Guanylyl Imidodiphosphate 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 228-231 3010521-2 1986 Gpp(NH)p and NaF are shown to be tightly bound to GTP-binding proteins (G-proteins) of outer segments of optic rods, additional activation of phosphodiesterase in the presence of Gpp(NH)p being observed after preincubation with NaF and subsequent washing of the membrane. Guanosine Triphosphate 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 3010521-2 1986 Gpp(NH)p and NaF are shown to be tightly bound to GTP-binding proteins (G-proteins) of outer segments of optic rods, additional activation of phosphodiesterase in the presence of Gpp(NH)p being observed after preincubation with NaF and subsequent washing of the membrane. Guanylyl Imidodiphosphate 179-187 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 3010521-4 1986 It is found that (NH4)2SO4 does not affect the basal activity of phosphodiesterase but inhibits the activating effect of Gpp(NH)p and NaF on the enzyme. Ammonium Sulfate 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 3010521-6 1986 Changes in the concentration of Mg2+ in the medium influence insignificantly the basal activity of phosphodiesterase but are necessary for manifestation of the activating effect of Gpp(NH)p and NaF. magnesium ion 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 194-197 3085668-1 1986 Addition of NaF to washed platelets produces a dose-dependent and transient elevation of the intracellular free calcium concentration ([Ca++]i), thromboxane B2 (TxB2) generation and dense granule release, all of which are significantly inhibited when the extracellular calcium concentration ([Ca++]e) is reduced with EGTA. Calcium 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 3085668-1 1986 Addition of NaF to washed platelets produces a dose-dependent and transient elevation of the intracellular free calcium concentration ([Ca++]i), thromboxane B2 (TxB2) generation and dense granule release, all of which are significantly inhibited when the extracellular calcium concentration ([Ca++]e) is reduced with EGTA. Thromboxane B2 145-159 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 3085668-1 1986 Addition of NaF to washed platelets produces a dose-dependent and transient elevation of the intracellular free calcium concentration ([Ca++]i), thromboxane B2 (TxB2) generation and dense granule release, all of which are significantly inhibited when the extracellular calcium concentration ([Ca++]e) is reduced with EGTA. Calcium 269-276 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 3085668-1 1986 Addition of NaF to washed platelets produces a dose-dependent and transient elevation of the intracellular free calcium concentration ([Ca++]i), thromboxane B2 (TxB2) generation and dense granule release, all of which are significantly inhibited when the extracellular calcium concentration ([Ca++]e) is reduced with EGTA. Egtazic Acid 317-321 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 3085668-4 1986 Pretreatment of the platelets with the selective protein kinase C inhibitor H7 prevents TPA induced inhibition of NaF mediated rise in [Ca++]i and TxB2 generation. Tetradecanoylphorbol Acetate 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 114-117 3085668-5 1986 Thus we propose that NaF induced calcium mobilisation is analogous to receptor-operated calcium mobilisation in platelets, as it is readily inhibited by protein kinase C activation or by the reduction of [Ca++]e and is independent of platelet cyclo-oxygenase activity. Calcium 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 3085668-5 1986 Thus we propose that NaF induced calcium mobilisation is analogous to receptor-operated calcium mobilisation in platelets, as it is readily inhibited by protein kinase C activation or by the reduction of [Ca++]e and is independent of platelet cyclo-oxygenase activity. Calcium 88-95 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 3001042-2 1986 At millimolar concentrations, reagent grade NaF inhibited glucose-6-P hydrolysis and protected the enzyme against inactivation induced by heat in the presence of 0.025% (w/v) Triton X-100 or by reaction of the catalytic site with the histidine-specific reagent, diethyl pyrocarbonate. Histidine 234-243 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 3001042-2 1986 At millimolar concentrations, reagent grade NaF inhibited glucose-6-P hydrolysis and protected the enzyme against inactivation induced by heat in the presence of 0.025% (w/v) Triton X-100 or by reaction of the catalytic site with the histidine-specific reagent, diethyl pyrocarbonate. Diethyl Pyrocarbonate 262-283 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 3001042-3 1986 The presence of millimolar EDTA in all test systems abolished the effectiveness of NaF, yet EDTA by itself was without significant influence on the kinetics of phosphohydrolase reaction, the thermal stability of the enzyme or its reactivity with diethyl pyrocarbonate. Edetic Acid 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 3001042-4 1986 Although ultrapure NaF was ineffectual in all test systems, its potency as a competitive inhibitor or protective agent was markedly increased by micromolar AlCl3 or when assays were carried out in flint glass test tubes. Aluminum Chloride 156-161 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 3768209-5 1986 Fourteen-day-old chicks treated with NaF (4.2 mM NaF in the drinking water) for 2 weeks showed increases in bone-forming surface in the tibial metaphysis (130% of untreated controls, P less than 0.002), with no change in the number of osteoblasts per length of forming surface (104% of control). Drinking Water 60-74 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 3768198-1 1986 The benefit of sodium fluoride (NaF) in the therapy of osteoporosis is still controversial. Sodium Fluoride 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 3768209-1 1986 Sodium fluoride (NaF) is the single most effective agent for increasing bone volume in the osteoporotic skeleton. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 3768209-6 1986 The NaF dose dependence of the change in bone-forming surface was biphasic, being optimal at 23 microM fluoride. Fluorides 103-111 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 3768209-5 1986 Fourteen-day-old chicks treated with NaF (4.2 mM NaF in the drinking water) for 2 weeks showed increases in bone-forming surface in the tibial metaphysis (130% of untreated controls, P less than 0.002), with no change in the number of osteoblasts per length of forming surface (104% of control). Drinking Water 60-74 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 3768209-7 1986 Linear correlations were observed between dietary NaF and serum fluoride (r = 0.996, P less than 0.001), and serum fluoride and bone fluoride concentrations (r = 0.98, P less than 0.001). Fluorides 64-72 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 3793326-8 1986 Clofazimine is not an oxidising agent nor did it stimulate membrane-associated oxidative metabolism in CGD or NaF-pulsed normal PMNL. Clofazimine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 3013404-0 1986 Fluoride uptake from an anti-calculus NaF dentifrice in vitro. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 3457629-3 1986 A carboxylic esterase isoenzyme which can be inhibited completely and selectively by sodium fluoride (NaF) was demonstrated by isoelectric focusing on horizontal polyacrylamide gels. Sodium Fluoride 85-100 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 3457629-3 1986 A carboxylic esterase isoenzyme which can be inhibited completely and selectively by sodium fluoride (NaF) was demonstrated by isoelectric focusing on horizontal polyacrylamide gels. polyacrylamide 162-176 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 3025924-10 1986 Human adenylate cyclase obtained from platelets and lymphocytes is activated by micromolar amounts of aluminum in the presence of NaF. Aluminum 102-110 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 3868620-3 1985 One isoenzyme consisting of one or two components (bands) could be completely and selectively inhibited by addition of 40 mM sodium fluoride (NaF) to the staining bath. Sodium Fluoride 125-140 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 4092416-1 1985 In sixteen patients subjected to intestinal surgery, the transport of sodium fluorescein (Na-F) was measured between the mucosal and serosal-muscular layers. Fluorescein 70-88 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 2933233-2 1985 Fluorescein flowmetry implies the measurement of capillary blood flow, expressed as an index between the maximum fluorescence after the first circulatory passage of sodium fluorescein (NaF) and the rise time, defined as the time interval between ten and 90 percent of the maximum fluorescence. Fluorescein 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 2933233-2 1985 Fluorescein flowmetry implies the measurement of capillary blood flow, expressed as an index between the maximum fluorescence after the first circulatory passage of sodium fluorescein (NaF) and the rise time, defined as the time interval between ten and 90 percent of the maximum fluorescence. Fluorescein 165-183 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 2997209-2 1985 Treatment of isolated hepatocytes with NaF produced a concentration-dependent activation of phosphorylase, inactivation of glycogen synthase, efflux of Ca2+, rise in cytosolic free Ca2+ ([Ca2+]i), increase in myo-inositol-1,4,5,-P3 levels, decrease in phosphatidylinositol-4,5-P2 levels, and increase in 1,2-diacylglycerol levels. myo-inositol-1,4,5,-p3 209-231 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 2997209-6 1985 The effects of low doses of NaF (2-15 mM) to inhibit basal or glucagon-stimulated cAMP accumulation, mobilize Ca2+, activate phosphorylase, and inactivate glycogen synthase were all potentiated by AlCl3. Aluminum Chloride 197-202 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 2997209-6 1985 The effects of low doses of NaF (2-15 mM) to inhibit basal or glucagon-stimulated cAMP accumulation, mobilize Ca2+, activate phosphorylase, and inactivate glycogen synthase were all potentiated by AlCl3. Cyclic AMP 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 2997209-2 1985 Treatment of isolated hepatocytes with NaF produced a concentration-dependent activation of phosphorylase, inactivation of glycogen synthase, efflux of Ca2+, rise in cytosolic free Ca2+ ([Ca2+]i), increase in myo-inositol-1,4,5,-P3 levels, decrease in phosphatidylinositol-4,5-P2 levels, and increase in 1,2-diacylglycerol levels. phosphatidylinositol-4,5-p2 252-279 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 2997209-2 1985 Treatment of isolated hepatocytes with NaF produced a concentration-dependent activation of phosphorylase, inactivation of glycogen synthase, efflux of Ca2+, rise in cytosolic free Ca2+ ([Ca2+]i), increase in myo-inositol-1,4,5,-P3 levels, decrease in phosphatidylinositol-4,5-P2 levels, and increase in 1,2-diacylglycerol levels. 1,2-diacylglycerol 304-322 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 2997209-4 1985 Maximum effects on Ca2+ efflux, [Ca2+]i, glycogen synthase, and phosphorylase were observed with 15 mM NaF, whereas myo-inositol-1,4,5-P3 and 1,2-diacylglycerol levels were maximally stimulated by 50 mM NaF. 1,2-diacylglycerol 142-160 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 2997209-5 1985 The levels of intracellular cAMP were decreased by NaF (up to 10 mM) in the absence or presence of glucagon (0.1-1 nM) or forskolin (2 microM). Cyclic AMP 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 2997209-6 1985 The effects of low doses of NaF (2-15 mM) to inhibit basal or glucagon-stimulated cAMP accumulation, mobilize Ca2+, activate phosphorylase, and inactivate glycogen synthase were all potentiated by AlCl3. Glucagon 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 2995338-3 1985 Gs and Gi can be activated by NaF with AlCl3 as well as by agonists acting through specific receptors. Aluminum Chloride 39-44 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 2995338-6 1985 Inhibition by NaF was enhanced synergistically by AlCl3 which alone only slightly inhibited GTPase activity. Aluminum Chloride 50-55 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 4006409-1 1985 The present work represents an attempt to develop a method for measuring relative blood flow in intestinal capillaries, by the use of sodium fluorescein (Na-F) as an indicator substance. Fluorescein 134-152 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 2994645-2 1985 When G-protein was present NaF, at millimolar concentrations, stimulated PDE activity however, in a G-protein free extract, cGMP hydrolysis was inhibited by high fluoride concentrations. Fluorides 162-170 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 2415257-7 1985 The binding of tritium-labeled alpha-BT and GABA to the membranes was depressed by both ouabain-containing and K-free solutions and also by compounds (theophylline and NaF) which increase the levels of intracellular ATP. Tritium 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 2415257-7 1985 The binding of tritium-labeled alpha-BT and GABA to the membranes was depressed by both ouabain-containing and K-free solutions and also by compounds (theophylline and NaF) which increase the levels of intracellular ATP. alpha-bt 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 2415257-7 1985 The binding of tritium-labeled alpha-BT and GABA to the membranes was depressed by both ouabain-containing and K-free solutions and also by compounds (theophylline and NaF) which increase the levels of intracellular ATP. gamma-Aminobutyric Acid 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 2415257-7 1985 The binding of tritium-labeled alpha-BT and GABA to the membranes was depressed by both ouabain-containing and K-free solutions and also by compounds (theophylline and NaF) which increase the levels of intracellular ATP. Adenosine Triphosphate 216-219 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 2985653-5 1985 Gel filtration of AM culture supernatants with a G-50 Sephadex column allowed isolation of a 6,000-D neutrophil-activating factor (NAF) that was resistant to heat (56 degrees C, 30 min). sephadex 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 4039272-2 1985 There is an increase in the number of [3H]forskolin binding sites when membranes are incubated with GppNHp or NaF in the presence of magnesium. Magnesium 133-142 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 4040041-2 1985 Ethanol up to a concentration of 5% (v/v) was without effect on basal luteal adenylyl cyclase activity, but markedly potentiated stimulation of NaF and hCG in a dose-dependent manner. Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 144-147 4040041-4 1985 Maximal NaF and hCG responsiveness of adenylyl cyclase activity was observed at 5% ethanol and reached values 80% and 100% higher than controls without ethanol, respectively. Ethanol 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 4040041-4 1985 Maximal NaF and hCG responsiveness of adenylyl cyclase activity was observed at 5% ethanol and reached values 80% and 100% higher than controls without ethanol, respectively. Ethanol 152-159 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 4040041-9 1985 These data indicate that the acute effects of ethanol inhibit forskolin-stimulated adenylyl cyclase at concentrations potentiating stimulatory effects of NaF and of hCG, and that the synergistic interaction of ethanol and gonadotropin stimulation of adenylyl cyclase is, at least in part, due to an increase in the functional coupling of the occupied hCG-receptor complex with the components of the enzyme system. Ethanol 46-53 C-X-C motif chemokine ligand 8 Homo sapiens 154-157 4040041-9 1985 These data indicate that the acute effects of ethanol inhibit forskolin-stimulated adenylyl cyclase at concentrations potentiating stimulatory effects of NaF and of hCG, and that the synergistic interaction of ethanol and gonadotropin stimulation of adenylyl cyclase is, at least in part, due to an increase in the functional coupling of the occupied hCG-receptor complex with the components of the enzyme system. Colforsin 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 154-157 4039272-0 1985 Regulation of [3H]forskolin binding to human platelet membranes by GppNHp, NaF, and prostaglandin E1. Tritium 15-17 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 4039272-0 1985 Regulation of [3H]forskolin binding to human platelet membranes by GppNHp, NaF, and prostaglandin E1. Colforsin 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 4039272-2 1985 There is an increase in the number of [3H]forskolin binding sites when membranes are incubated with GppNHp or NaF in the presence of magnesium. Tritium 39-41 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 4039272-2 1985 There is an increase in the number of [3H]forskolin binding sites when membranes are incubated with GppNHp or NaF in the presence of magnesium. Colforsin 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 2984996-2 1985 Bone resorption was increased when embryonic chick tibiae were exposed to ethanol at 0.03-0.3% (v/v), and bone formation was inhibited when tibiae were exposed to 0.2% ethanol in the presence of NaF or parathyroid hormone (P less than 0.01 for each). Ethanol 168-175 C-X-C motif chemokine ligand 8 Homo sapiens 195-198 2984996-5 1985 Paradoxically, mitogenic doses of ethanol prevented the effects of two other mitogens, NaF and human skeletal growth factor, to increase bone cell proliferation (P less than 0.001). Ethanol 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 2985653-8 1985 NAF was only minimally chemotactic and eluted from Sephadex G-50 with particles of a different molecular size than those of AM-derived chemotactic factors (i.e., approximately 10,000 D and less than 500 D). sephadex 51-64 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2985653-9 1985 Preincubation of neutrophils with NAF resulted in greater release of superoxide anion upon their subsequent stimulation by either bacterial phagocytosis or by phorbol myristate acetate, as compared with control neutrophils stimulated in a like manner. Superoxides 69-85 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 2985653-9 1985 Preincubation of neutrophils with NAF resulted in greater release of superoxide anion upon their subsequent stimulation by either bacterial phagocytosis or by phorbol myristate acetate, as compared with control neutrophils stimulated in a like manner. Tetradecanoylphorbol Acetate 159-184 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 3977849-7 1985 Addition of La3+ directly to the adenylate cyclase assay resulted in a partial inhibition of TSH- and NaF-stimulated activity, with 50% inhibition produced by 5.1 microM and 4.0 microM-La3+ respectively. lanthanum(3+) 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 10031523-0 1985 Observation of surface optical phonons in NaF(001) by inelastic He-atom scattering. Helium 64-66 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 2983174-6 1985 We also found that calcium reduced enzyme stimulation by forskolin and the GTP analog, guanyl 5"-yl imidodiphosphate [GMP-P(NH)P] in a dose-related manner and that activation by NaF was less sensitive to inhibition by calcium. Calcium 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 2983174-6 1985 We also found that calcium reduced enzyme stimulation by forskolin and the GTP analog, guanyl 5"-yl imidodiphosphate [GMP-P(NH)P] in a dose-related manner and that activation by NaF was less sensitive to inhibition by calcium. Colforsin 57-66 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 2983174-6 1985 We also found that calcium reduced enzyme stimulation by forskolin and the GTP analog, guanyl 5"-yl imidodiphosphate [GMP-P(NH)P] in a dose-related manner and that activation by NaF was less sensitive to inhibition by calcium. Guanosine Triphosphate 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 2983174-6 1985 We also found that calcium reduced enzyme stimulation by forskolin and the GTP analog, guanyl 5"-yl imidodiphosphate [GMP-P(NH)P] in a dose-related manner and that activation by NaF was less sensitive to inhibition by calcium. guanyl 5"-yl imidodiphosphate 87-116 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 2983174-6 1985 We also found that calcium reduced enzyme stimulation by forskolin and the GTP analog, guanyl 5"-yl imidodiphosphate [GMP-P(NH)P] in a dose-related manner and that activation by NaF was less sensitive to inhibition by calcium. Guanylyl Imidodiphosphate 118-128 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 2983174-6 1985 We also found that calcium reduced enzyme stimulation by forskolin and the GTP analog, guanyl 5"-yl imidodiphosphate [GMP-P(NH)P] in a dose-related manner and that activation by NaF was less sensitive to inhibition by calcium. Calcium 218-225 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 2983174-7 1985 Accordingly, at 2.5 mM CaCl2, guanyl nucleotide and forskolin stimulations were inhibited 96% and 86%, respectively, while NaF stimulation was reduced by 40%. Calcium Chloride 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 18963835-0 1985 Effect of EDTA/NaF solutions on the orion Cu(II) ion-selective electrode. cu(ii) 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 18963835-2 1985 This effect has been found to arise from an enhanced rate of response to changes in EDTA concentration when the electrode has been exposed to an EDTA/NaF medium for prolonged periods. Edetic Acid 84-88 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 18963835-2 1985 This effect has been found to arise from an enhanced rate of response to changes in EDTA concentration when the electrode has been exposed to an EDTA/NaF medium for prolonged periods. Edetic Acid 145-149 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 3977849-7 1985 Addition of La3+ directly to the adenylate cyclase assay resulted in a partial inhibition of TSH- and NaF-stimulated activity, with 50% inhibition produced by 5.1 microM and 4.0 microM-La3+ respectively. lanthanum(3+) 185-189 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 3977849-8 1985 Particulate preparations with La3+ showed a decrease of TSH- and NaF-stimulated adenylate cyclase activity (approx. lanthanum(3+) 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 3855886-6 1985 The enamel biopsy data showed that the fluoride uptake resulting from 0.2% NaF alone was not statistically significant, whereas uptake produced by the DCPD-forming plus NaF rinses was significant. Fluorides 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 2982913-8 1985 NaF (10 mM) also activated the cyclase system and produced the same magnitude of response as maximum glucagon activation. Glucagon 101-109 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3873544-3 1985 NaF-activated preparations were also subjected to gel filtration in the presence of CHAPS. 3-((3-cholamidopropyl)dimethylammonium)-1-propanesulfonate 84-89 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 3857545-0 1985 [Effects of NaF on phenol and indole production in human saliva]. Phenol 19-25 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 2984059-2 1985 The response to Gpp(NH)p, ACTH1-24 + Gpp(NH)p and NaF was significantly lower in membranes from fetuses than from neonate lambs, whereas the response to forskolin was similar. Phosphorus 7-8 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 3857545-0 1985 [Effects of NaF on phenol and indole production in human saliva]. indole 30-36 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 3857030-4 1985 Increasing the packing density of killed plaque residue of Streptococcus sanguis cells reduced D. Pre-incubation of plaque residue with sucrose or sucrose + NaF reduced D for lactate. Lactic Acid 175-182 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 3857987-0 1985 Fluoride uptake by dentin surfaces following topical application of TiF4, NaF and fluoride varnishes in vivo. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 6440486-4 1984 NaF-Activated preparations were also subjected to gel filtration in the presence of Chaps, in which case both the catalytic activity and G/F emerged in the activated state. 3-((3-cholamidopropyl)dimethylammonium)-1-propanesulfonate 84-89 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 6440486-6 1984 NaF and guanine nucleotide sensitivity could be reconstituted in nonactivated preparations of C by G/F in the presence of NaF or guanylylimidodiphosphate. Guanine Nucleotides 8-26 C-X-C motif chemokine ligand 8 Homo sapiens 122-125 6440486-6 1984 NaF and guanine nucleotide sensitivity could be reconstituted in nonactivated preparations of C by G/F in the presence of NaF or guanylylimidodiphosphate. Guanylyl Imidodiphosphate 129-153 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 6397354-0 1984 [Fluoride loss from demineralized enamel after the application of different concentrations of NaF and Na-MFP solutions in an artificial mouth]. Fluorides 1-9 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 6209573-3 1984 The action of beta-aminoethylisothiouronium bromide hydrobromide (AET) and sodium fluoride (NaF) on the clastogenic activity of Trenimon, cyclophosphamide, and bleomycin was tested on cultures of human peripheral lymphocytes with and without the addition of rat liver S9 mix. Bleomycin 160-169 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 18963717-1 1984 The solubilities of LiF, NaF, KF, RbF and CsF in acetonitrile, acetone, tetrahydrofuran, dimethylformamide, benzene and cyclohexane have been determined with and without a crown ether (usually 0.1 M 18-crown-6) present. Cyclohexane 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 3864545-0 1985 Time dependence of F uptake in demineralized enamel from 1,000-ppm fluoride NaF and Na2FPO3 solutions. Fluorine 19-20 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 6434290-8 1984 NaF- and forskolin-stimulated enzyme activities were significantly increased by Gs in both the presence and absence of Gpp(NH)p (100 microM). Guanylyl Imidodiphosphate 119-127 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 6373000-4 1984 Furthermore, the nonspecific esterase activity of TPA-treated cells and weak activity in 10% of untreated cells was strongly inhibited by NaF, a characteristic of monocytic series of cells. Tetradecanoylphorbol Acetate 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 138-141 6592201-4 1984 The enamel in white spots from users of the 0.243% NaF dentifrice had a mean fluoride content higher than that from users of the 0.4% SnF2 dentifrice. Fluorides 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 6588075-0 1984 Fluoride levels in dentin after iontophoresis of 2% NaF. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 6086524-5 1984 The neutrophil"s response to NaF was blunted by sulfinpyrazone (KI50 = 400 microM) and phenylbutazone (KI50 = 65 microM), but was unaffected by indomethacin. Sulfinpyrazone 48-62 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 6086524-5 1984 The neutrophil"s response to NaF was blunted by sulfinpyrazone (KI50 = 400 microM) and phenylbutazone (KI50 = 65 microM), but was unaffected by indomethacin. ki50 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 6086524-5 1984 The neutrophil"s response to NaF was blunted by sulfinpyrazone (KI50 = 400 microM) and phenylbutazone (KI50 = 65 microM), but was unaffected by indomethacin. Phenylbutazone 87-101 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 6738571-1 1984 The effect of treatment of cultured human oral keratinocytes with sodium fluoride (NaF) has been investigated with respect to induction of unscheduled DNA synthesis (UDS). Sodium Fluoride 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 6325278-4 1984 Within an alkali cation series (e.g. NaCH3CO2, NaF, NaCl, NaBr, NaNO3, NaI or a similar potassium series) the affinity decreased with decreasing B coefficient of viscosity. Sodium Chloride 52-56 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 6325411-12 1984 Whereas extracts from control and butyrate-treated HeLa were equally effective in restoring NaF-stimulated activity in cyc- membranes, extracts from control HeLa were less efficient in reconstituting isoproterenol- and prostaglandin E1-stimulated activities. Butyrates 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 6325278-4 1984 Within an alkali cation series (e.g. NaCH3CO2, NaF, NaCl, NaBr, NaNO3, NaI or a similar potassium series) the affinity decreased with decreasing B coefficient of viscosity. Sodium Iodide 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 6325278-4 1984 Within an alkali cation series (e.g. NaCH3CO2, NaF, NaCl, NaBr, NaNO3, NaI or a similar potassium series) the affinity decreased with decreasing B coefficient of viscosity. Potassium 88-97 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 6322840-8 1984 On photoactivation with 30 microM DAN, the NaF-stimulated adenylate cyclase was inhibited, but this effect was completely prevented by added GSH. dan 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 6230119-4 1984 Inhibition studies of cytochemical ANAE activity with sodium fluoride (NaF) show that the presence of NaF-sensitive or NaF-resistant ANAE enzymes is often unrelated to the diagnostic category of acute leukemia. Sodium Fluoride 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 6230119-4 1984 Inhibition studies of cytochemical ANAE activity with sodium fluoride (NaF) show that the presence of NaF-sensitive or NaF-resistant ANAE enzymes is often unrelated to the diagnostic category of acute leukemia. Sodium Fluoride 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 6230119-4 1984 Inhibition studies of cytochemical ANAE activity with sodium fluoride (NaF) show that the presence of NaF-sensitive or NaF-resistant ANAE enzymes is often unrelated to the diagnostic category of acute leukemia. Sodium Fluoride 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 6322840-8 1984 On photoactivation with 30 microM DAN, the NaF-stimulated adenylate cyclase was inhibited, but this effect was completely prevented by added GSH. Glutathione 141-144 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 6418524-6 1984 Addition of 0.5 mM EGTA to the reaction mixture resulted in an approximate 30% increase in basal adenylate cyclase activity and a similar percentage increase in the activity measured in the presence of guanosine triphosphate or NaF, known activators of parathyroid adenylate cyclase. Egtazic Acid 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 228-231 6690596-2 1984 NaF and ouabain were used to inhibit adenosine triphosphatases (ATP) and NaF and isoproterenol were used as activators of AC. Ouabain 8-15 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 6594786-11 1984 It was concluded that the posteruptively increased enamel fluorine concentration probably contributes to the caries-preventive effect of NaF tablets. Fluorine 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 137-140 6293548-1 1982 We have previously described a phosphotyrosylprotein phosphatase in membrane vesicles from human epidermoid carcinoma A431 cells which is inhibited by micromolar concentration of Zn2+ and is insensitive to ethylenediaminetetraacetic acid (EDTA) and NaF [Brautigan, D. L., Bornstein, P., & Gallis, B. Zinc 179-183 C-X-C motif chemokine ligand 8 Homo sapiens 249-252 6315795-3 1983 Thus, upon exposure of C62B cells to catecholamine a rapid decline (t 1/2 = 6-8 min) in isoproterenol-stimulated adenylate cyclase activity occurs with minimal loss in basal or NaF-stimulated activity. Catecholamines 37-50 C-X-C motif chemokine ligand 8 Homo sapiens 177-180 6836584-1 1983 The present study describes the effect of fluoride (10 mg NaF/kg body weight/day) on the total protein-bound sialic acid and ceruloplasmin levels in rabbit serum after receiving sodium fluoride intragastrically for 3, 5, 8 and 10 months. Fluorides 42-50 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 6961976-4 1982 The addition of fluoride (NaF or MFP) in mouthrinses and toothpastes significantly reduced the number of new carious lesions. Fluorides 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 6294425-5 1982 The production of cAMP following direct stimulation of adenylate cyclase by NaF was contrasted with receptor mediated activation of adenylate cyclase by prostaglandin E1 (PGE1) in disrupted platelet preparations from schizophrenics and normal controls. Cyclic AMP 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 6294425-6 1982 cAMP formation stimulated by NaF was not different in platelets of schizophrenics as compared to controls, however, platelets of schizophrenics showed reduced response to PGE1 stimulation. Cyclic AMP 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 6712979-5 1984 The formation of [3H]cholesteryl esters was not significantly affected by energy poisons (NaF and KCN) but was inhibited (to 50%) by chloroquine at 50 microM. [3h]cholesteryl esters 17-39 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 6296138-5 1983 GDP also inhibited cyclase activity stimulated by NaF with UDP but did only slightly without UDP. Guanosine Diphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 6296138-5 1983 GDP also inhibited cyclase activity stimulated by NaF with UDP but did only slightly without UDP. Uridine Diphosphate 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 6836584-1 1983 The present study describes the effect of fluoride (10 mg NaF/kg body weight/day) on the total protein-bound sialic acid and ceruloplasmin levels in rabbit serum after receiving sodium fluoride intragastrically for 3, 5, 8 and 10 months. N-Acetylneuraminic Acid 109-120 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 6293548-1 1982 We have previously described a phosphotyrosylprotein phosphatase in membrane vesicles from human epidermoid carcinoma A431 cells which is inhibited by micromolar concentration of Zn2+ and is insensitive to ethylenediaminetetraacetic acid (EDTA) and NaF [Brautigan, D. L., Bornstein, P., & Gallis, B. Edetic Acid 239-243 C-X-C motif chemokine ligand 8 Homo sapiens 249-252 6293548-9 1982 The phosphatase was inhibited by Zn2+ at micromolar concentrations (K0.5 with EGF receptor kinase = 5 X 10(-6) M; with CM-SC phosphorylase = 3.3 X 10(-5) M) but not by millimolar concentrations of EDTA and NaF. Zinc 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 206-209 7115353-3 1982 In plasma membranes from control cells in the presence of heat-inactivated human erythrocyte membranes both guanosine 5"-[beta, gamma-imido]triphosphate (p[NH]ppG) plus lutropin and NaF caused a 45--50-fold increase in cyclic AMP production over 30 min compared with 12--13 fold p[NH[ppG and 2--3-fold with lutropin alone. Cyclic AMP 219-229 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 7153474-4 1982 Only the second peak reduced the NaF stimulated cAMP production. Cyclic AMP 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 6291624-4 1982 Effects of GTP and GDP were indistinguishable in regard to their inhibitory effects on NaF-stimulated activities. Guanosine Triphosphate 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 6291624-4 1982 Effects of GTP and GDP were indistinguishable in regard to their inhibitory effects on NaF-stimulated activities. Guanosine Diphosphate 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 6291624-10 1982 GDP was less inhibitory than Gpp(NH)p to the NaF-stimulated adenylate cyclase activity. Guanosine Diphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 6291624-10 1982 GDP was less inhibitory than Gpp(NH)p to the NaF-stimulated adenylate cyclase activity. Guanylyl Imidodiphosphate 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 6291624-13 1982 (3) The nucleotide regulatory site is more inhibitory to the stimulation of the enzyme by NaF when occupied by Gpp[NH]p than GDP. Guanylyl Imidodiphosphate 111-119 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 6291624-13 1982 (3) The nucleotide regulatory site is more inhibitory to the stimulation of the enzyme by NaF when occupied by Gpp[NH]p than GDP. Guanosine Diphosphate 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 7115353-3 1982 In plasma membranes from control cells in the presence of heat-inactivated human erythrocyte membranes both guanosine 5"-[beta, gamma-imido]triphosphate (p[NH]ppG) plus lutropin and NaF caused a 45--50-fold increase in cyclic AMP production over 30 min compared with 12--13 fold p[NH[ppG and 2--3-fold with lutropin alone. nh[ppg 281-287 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 7115353-3 1982 In plasma membranes from control cells in the presence of heat-inactivated human erythrocyte membranes both guanosine 5"-[beta, gamma-imido]triphosphate (p[NH]ppG) plus lutropin and NaF caused a 45--50-fold increase in cyclic AMP production over 30 min compared with 12--13 fold p[NH[ppG and 2--3-fold with lutropin alone. Luteinizing Hormone 307-315 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 6177249-7 1982 In fact, the role of NaF therapy could already be taken over by diphosphonates currently under study. Diphosphonates 64-78 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 6951705-0 1982 [Fluoride uptake and retention in the dental enamel of adults after the application of NaF tablets and NaF gel in vivo]. Fluorides 1-9 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 6951705-0 1982 [Fluoride uptake and retention in the dental enamel of adults after the application of NaF tablets and NaF gel in vivo]. Fluorides 1-9 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 6961914-0 1982 Effect of extracellular polysaccharides on diffusion of NaF and [14C]-sucrose in human dental plaque and in sediments of the bacterium Streptococcus sanguis 804 (NCTC 10904). Polysaccharides 24-39 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 6961914-3 1982 sanguis 804 at 37 degrees C. There was a tendency for NaF and [14C]-sucrose to diffuse faster as the carbohydrate concentration in the sediments increased. Carbohydrates 101-113 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 6961914-4 1982 NaF diffused only 38 per cent more slowly in cell-free glucan sediment than in water, suggesting that glucan per se does not form a barrier to diffusion. Glucans 55-61 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 6961914-5 1982 The diffusion coefficient for NaF was positively correlated with carbohydrate concentration in individual plaque samples from 15 subjects and incubation of 3 plaque samples with sucrose resulted in both an increase in carbohydrate concentration in the plaque and an increase in D for NaF. Carbohydrates 65-77 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 6961914-5 1982 The diffusion coefficient for NaF was positively correlated with carbohydrate concentration in individual plaque samples from 15 subjects and incubation of 3 plaque samples with sucrose resulted in both an increase in carbohydrate concentration in the plaque and an increase in D for NaF. Sucrose 178-185 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 6961914-5 1982 The diffusion coefficient for NaF was positively correlated with carbohydrate concentration in individual plaque samples from 15 subjects and incubation of 3 plaque samples with sucrose resulted in both an increase in carbohydrate concentration in the plaque and an increase in D for NaF. Sucrose 178-185 C-X-C motif chemokine ligand 8 Homo sapiens 284-287 6961914-5 1982 The diffusion coefficient for NaF was positively correlated with carbohydrate concentration in individual plaque samples from 15 subjects and incubation of 3 plaque samples with sucrose resulted in both an increase in carbohydrate concentration in the plaque and an increase in D for NaF. Carbohydrates 218-230 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 7121252-2 1982 The dose of NaF was modified according to the serum fluoride concentration, which was kept as constant as possible between 0.20 and 0.25 microgram/ml. Fluorides 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 6263877-3 1981 The reconstitution process in the presence of guanyl-5"-yl imidodiphosphate or NaF is time-dependent, directly proportional to the quantity of erythrocyte protein added to the reconstitution system, and is only observed when Mg-ATP is used as substrate. Adenosine Triphosphate 225-231 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 7287864-3 1981 The activity of the enzyme was inhibited by preincubation of microsomes with ATP (4 mM) and was greatly reduced when microsomes were prepared from tissue homogenized in the presence of NaF (50 mM). Adenosine Triphosphate 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 19701426-0 1981 Laser-active, defect-stabilized F2+ center in NAF:OH- and dynamics of defect-stabilized center formation. f2+ 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 6946109-0 1981 Fluoride uptake from in situ brushing with a SnF2 and a NaF dentifrice. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 6946109-1 1981 Fluoride uptake into decalcified human enamel was determined from in situ brushing with a 0.40% SnF2-calcium pyrophosphate abrasive dentifrice, a 0.243% NaF-silica abrasive dentifrice, and a non-fluoride-silica abrasive placebo dentifrice. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 6946109-1 1981 Fluoride uptake into decalcified human enamel was determined from in situ brushing with a 0.40% SnF2-calcium pyrophosphate abrasive dentifrice, a 0.243% NaF-silica abrasive dentifrice, and a non-fluoride-silica abrasive placebo dentifrice. Silicon Dioxide 157-163 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 6946109-4 1981 The mean fluoride contents after use of the test dentifrices were 16.0, 8.4, and 4.6 micro/cm2 for the 0.243% NaF, the 0.40% SnF2, and the placebo dentifrice, respectively. Fluorides 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 7317821-5 1981 Activation of the heart and skeletal muscle enzyme by NaF and GPP(NH)P greatly reduced the Mg2+ requirement; this was seen with both particulate and solubilized preparations. magnesium ion 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 7315114-8 1981 Prior to incubation the erythrocytes were stored with NaF in order to reduce the total adenylate concentration. Adenosine Monophosphate 87-96 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 7207691-0 1981 A subacute fluoride intoxication during treatment of osteoporosis with sodium fluoride (NaF): case report. Fluorides 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 6935392-3 1981 The most elevated release of fluoride from the NaF containing--and the most protracted from the CaF2 containing--plates may be related to the solubilities of the compounds. Fluorides 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 7207691-0 1981 A subacute fluoride intoxication during treatment of osteoporosis with sodium fluoride (NaF): case report. Sodium Fluoride 71-86 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 7417708-3 1980 This drug-induced movement of 45Ca to membrane sites was blocked by depleting erythrocytes of adenosine triphosphate (ATP) or by incubating them with known inhibitors of endocytosis, NaF of N-ethylmaleimide (NEM). Ethylmaleimide 190-206 C-X-C motif chemokine ligand 8 Homo sapiens 183-186 7291201-6 1981 Prior to incubation the erythrocytes were stored with NaF in order to reduce the total adenylate concentration. Adenosine Monophosphate 87-96 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 7204643-2 1980 To test for the possible origin of these labeled cells from monocytes, we examined them for the presence of sodium fluoride- (NaF) sensitive non-specific esterase (NSE), an enzyme characteristic of monocytes. Sodium Fluoride 108-123 C-X-C motif chemokine ligand 8 Homo sapiens 126-129 6258579-11 1980 Half-maximum inhibition of the phosphatase by 5,5"-dithiobis-(2-nitrobenzoate), EDTA and NaF is obtained at 0.5 microM, 1 mM and 4 mM respectively. 5,5"-dithiobis-(2-nitrobenzoate) 46-78 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 6935963-1 1980 A laboratory study was carried out to evaluate the effectiveness of NaF and SnF2, when incorporated into zinc oxyphosphate cement, in reducing the solubility and increasing the microhardness of human enamel. zinc oxyphosphate 105-122 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 7417708-3 1980 This drug-induced movement of 45Ca to membrane sites was blocked by depleting erythrocytes of adenosine triphosphate (ATP) or by incubating them with known inhibitors of endocytosis, NaF of N-ethylmaleimide (NEM). Ethylmaleimide 208-211 C-X-C motif chemokine ligand 8 Homo sapiens 183-186 6932085-0 1980 Effect of mouthrinses with SnF2, LaCl3, NaF and chlorhexidine on the amount of lipoteichoic acid formed in plaque. lipoteichoic acid 79-96 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 6931113-2 1980 The sustained F-release was achieved by embedding NaF in ethyl cellulose and silicone polymer, both known to be nontoxic and insoluble in saliva. ethyl cellulose 57-72 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 7419155-1 1980 The plasma fluoride concentration after oral administration of 40 mg of NaF in delayed and nondelayed form depending on the thyroid function]. Fluorides 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 6251111-4 1980 Glutamic acid and aspartic acid together accounted for a total of 18 and 19% of the amino acids in purified preparations of NAF I and NAF II, respectively, whereas the basic amino acids lysine, arginine, and histidine represented <2 and 3% of the total residues. Glutamic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 6251111-4 1980 Glutamic acid and aspartic acid together accounted for a total of 18 and 19% of the amino acids in purified preparations of NAF I and NAF II, respectively, whereas the basic amino acids lysine, arginine, and histidine represented <2 and 3% of the total residues. Glutamic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 6251111-4 1980 Glutamic acid and aspartic acid together accounted for a total of 18 and 19% of the amino acids in purified preparations of NAF I and NAF II, respectively, whereas the basic amino acids lysine, arginine, and histidine represented <2 and 3% of the total residues. Aspartic Acid 18-31 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 6251111-4 1980 Glutamic acid and aspartic acid together accounted for a total of 18 and 19% of the amino acids in purified preparations of NAF I and NAF II, respectively, whereas the basic amino acids lysine, arginine, and histidine represented <2 and 3% of the total residues. Aspartic Acid 18-31 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 6768782-2 1980 Surfaces remineralized 25 hours in 0.4 mM NaF (8 ppm F-) dissolved slower in acid or in EDTA than those remineralized in the absence of F-. Edetic Acid 88-92 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 6108993-12 1980 The ATP hydrolysis activity was inhibited by NaF but unaffected by ouabain, vanadate, cytochalasin B, and various drugs known to influence ATPase activity of mitochondria. Adenosine Triphosphate 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 6934618-4 1980 Sucking NaF tablets caused a fall in initial pH and an increase in total calcium, while the amount of ionized calcium remained unchanged. Calcium 73-80 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 6934618-5 1980 The content of fluoride was high in saliva during sucking of NaF tablets. Fluorides 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 6929286-0 1980 Fluroide concentration in enamel treated with 50% phosphoric acid and NaF with subsequent decalcification in "acid-gel". fluroide 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 6246514-11 1980 Time course studies utilizing pyrophosphate as the phosphate source showed only one phase of phosphorylation that was strongly inhibited by micromolar levels of ATP as well as by NaF (5 mM). diphosphoric acid 30-43 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 7396871-9 1980 At high concentrations (greater than 3 mM) N alpha-tosylarginine methyl ester also inhibited NaF- and guanosine 5"-[beta gamma-imidol]-triphosphate-stimulated cyclase but in a reversible manner. n alpha-tosylarginine methyl ester 43-77 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 7396871-10 1980 7-Amino-1-chloro-3-L-tosylamidoheptan-2-one inhibited NaF-stimulated adenylate cyclase in two ways, as for human-choriogonadotropin-stimulated adenylate cyclase, but required 10--20-fold higher concentrations. 7-amino-1-chloro-3-l-tosylamidoheptan-2-one 0-43 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 6935030-0 1980 [Fluoride uptake and retention in the dental enamel after the application of NaF tablets in schoolchildren]. Fluorides 1-9 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 6246514-11 1980 Time course studies utilizing pyrophosphate as the phosphate source showed only one phase of phosphorylation that was strongly inhibited by micromolar levels of ATP as well as by NaF (5 mM). Phosphates 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 7009669-2 1980 Results indicated that 2.5% NaF in the etchant prevent the sealant bond, but addition of 0.02% NaF resulted in an increase in fluoride content of the enamel surface without a decrease in bond strength. Fluorides 126-134 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 6103847-3 1980 The present study analyzes the effects of heparin and sodium fluoride (NaF) on these changes. Sodium Fluoride 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 40394-5 1979 Incorporation of leucine was then stimulated by low fluoride concentrations (0.5 and 0.9 mM), and the effect on thymidine incorporation was eradicated up to 1.3 mM-NaF. Leucine 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 164-167 6928001-4 1980 Smooth surface adherence by both fluoride-sensitive and -resistant strains of S. mutans 6715 in a tooth model system was slightly diminished by 1% NaF gel. Fluorides 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 147-150 6938993-1 1980 Three types of sustained and controlled release dosage forms of sodium fluoride (NaF) for the prevention of dental caries are reviewed. Sodium Fluoride 64-79 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 6938993-2 1980 Sustained release NaF tablets or capsules have prolonged the elevation of saliva and plasma fluoride levels in both animal and human studies when compared to conventional NaF tablets. Fluorides 92-100 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 6938993-3 1980 In vitro studies have shown that aerosol application of NaF-containing microcapsules to the tooth surface may prolong the retention of a given dose of fluoride in the mouth and also increase enamel uptake of fluoride. Fluorides 151-159 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 6938993-3 1980 In vitro studies have shown that aerosol application of NaF-containing microcapsules to the tooth surface may prolong the retention of a given dose of fluoride in the mouth and also increase enamel uptake of fluoride. Fluorides 208-216 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 41586-5 1979 The solubilized monoacylglycerol hydrolase from platelets was optimally active at pH between 7 and 8 and at ionic strength corresponding to [NaCl] between 0.1 and 0.3 M. The optimal assay temperature was 37 degrees C. The enzyme activity was sensitive to HgCl2 but not to NaF. Sodium Chloride 141-145 C-X-C motif chemokine ligand 8 Homo sapiens 272-275 28310569-0 1980 The simultaneous effect of soil-borne NaF and air pollutant SO2 on CO2-uptake and pollutant accumulation. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 263633-1 1979 The complete neglect of differential overlap method is used to investigate the binding of LiF, LiCl, NaF, and NaCl to N-methyl acetamide (NMA) as a model for these ions binding to a peptide moiety. N-methylacetamide 118-136 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 263633-1 1979 The complete neglect of differential overlap method is used to investigate the binding of LiF, LiCl, NaF, and NaCl to N-methyl acetamide (NMA) as a model for these ions binding to a peptide moiety. N-methylacetamide 138-141 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 40394-5 1979 Incorporation of leucine was then stimulated by low fluoride concentrations (0.5 and 0.9 mM), and the effect on thymidine incorporation was eradicated up to 1.3 mM-NaF. Thymidine 112-121 C-X-C motif chemokine ligand 8 Homo sapiens 164-167 427219-6 1979 Stimulation by adenosine was additive with the effects of GMP-P(NH)P, and alpha- or beta-adrenergic stimulation, but was abolished by prostaglandin E1 or by NaF. Adenosine 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 379285-1 1979 The tensile bond strength of Epoxylite 9075 and Enamelite to enamel treated with NaF and SnF2, at two concentrations, in the etching acid (H3PO4) was determined. epoxylite 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 379285-1 1979 The tensile bond strength of Epoxylite 9075 and Enamelite to enamel treated with NaF and SnF2, at two concentrations, in the etching acid (H3PO4) was determined. etching acid 125-137 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 379285-4 1979 Incorporation of NaF or SnF2 in the etching solutions highly increased the fluoride concentration of enamel. Fluorides 75-83 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 379285-5 1979 The fluoride increase dependend on the fluoride concentration of the etching solution and was greater for NaF than SnF2. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 379285-5 1979 The fluoride increase dependend on the fluoride concentration of the etching solution and was greater for NaF than SnF2. Fluorides 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 293239-2 1979 The combined effect of fissure sealing and topical fluoride therapy with 2% NaF gel resulted over the 2 years in an increase in the proportion of caries-free permanent first molars from 50% to 81% in the 1st grade. Fluorides 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 427219-7 1979 Prostaglandin E1 and NaF increased the sensitivity of adenylate cyclase to inhibition by adenosine. Adenosine 89-98 C-X-C motif chemokine ligand 8 Homo sapiens 0-24 368092-0 1979 Treatment of enamel with 50% phosphoric acid containing 0.5% and 2% NaF. phosphoric acid 29-44 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 292158-2 1979 The amount of fluoride extractable from dentrifrices containing 0.1% NaF and the fluoride ion activity were not reduced by the addition of 2% chlorhexidine digluconate. Fluorides 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 25551-3 1978 NaF, at 1 and 5 mM, progressively increased this parameter while norepinephrine caused a similar effect at 10(-3) but not at 10(-6) M. Phentolamine (1 mM) blocked the stimulatory action of TSH; propranolol and atropine did not. Phentolamine 135-147 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 759278-1 1979 The bioavailability of Ossin, a drug for the treatment of osteoporosis, containing 40 mg of NaF, was investigated. Sodium Fluoride 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 580872-1 1978 Thyrotropin (TSH)- and sodium fluoride (NaF)-sensitive adenylate cyclase (AC) activity was measured in ten cases of "cold" thyroid nodules and compared with perinodular tissue. Sodium Fluoride 23-38 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 207727-2 1978 The present study examined PMN CL in the absence of phagocytosis using sodium fluoride (NaF), a nonparticulate agent and known stimulator of cellular oxidative metabolism. Sodium Fluoride 71-86 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 207727-5 1978 Superoxide anion production correlated closely with CL responses in NaF-treated human PMNs. Superoxides 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 207727-6 1978 CL responses were completely suppressed in the presence of the oxidative metabolic inhibitors, iodoacetamide, and N-ethylmalemide; and were partially suppressed in the presence of either superoxide dismutase or sodium azide.CL responses of NaF-treated PMNs were significantly lower than responses generated by PMNs phagocytizing opsonized yeast. Iodoacetamide 95-108 C-X-C motif chemokine ligand 8 Homo sapiens 240-243 207727-6 1978 CL responses were completely suppressed in the presence of the oxidative metabolic inhibitors, iodoacetamide, and N-ethylmalemide; and were partially suppressed in the presence of either superoxide dismutase or sodium azide.CL responses of NaF-treated PMNs were significantly lower than responses generated by PMNs phagocytizing opsonized yeast. n-ethylmalemide 114-129 C-X-C motif chemokine ligand 8 Homo sapiens 240-243 207727-6 1978 CL responses were completely suppressed in the presence of the oxidative metabolic inhibitors, iodoacetamide, and N-ethylmalemide; and were partially suppressed in the presence of either superoxide dismutase or sodium azide.CL responses of NaF-treated PMNs were significantly lower than responses generated by PMNs phagocytizing opsonized yeast. Sodium Azide 211-223 C-X-C motif chemokine ligand 8 Homo sapiens 240-243 212438-5 1978 It is reported herein that the degradation of receptor-bound human choriogonadotropin is an energy-dependent process, which can be inhibited by compounds that interfere with glycolysis or oxidative phosphorylation (e.g. NaF, NaN3, NaCN, and 2-deoxyglucose). Sodium Azide 225-229 C-X-C motif chemokine ligand 8 Homo sapiens 220-223 212438-5 1978 It is reported herein that the degradation of receptor-bound human choriogonadotropin is an energy-dependent process, which can be inhibited by compounds that interfere with glycolysis or oxidative phosphorylation (e.g. NaF, NaN3, NaCN, and 2-deoxyglucose). Sodium Cyanide 231-235 C-X-C motif chemokine ligand 8 Homo sapiens 220-223 212438-5 1978 It is reported herein that the degradation of receptor-bound human choriogonadotropin is an energy-dependent process, which can be inhibited by compounds that interfere with glycolysis or oxidative phosphorylation (e.g. NaF, NaN3, NaCN, and 2-deoxyglucose). Deoxyglucose 241-255 C-X-C motif chemokine ligand 8 Homo sapiens 220-223 707137-2 1978 In intact, sensitive cells, 6 mM NaF had no effect on glycolysis, whereas in homogenates, from both resistant and sensitive cells, lactate production was blocked by 6 mM NaF, indicating the cell membrane to be a barrier to fluoride. Lactic Acid 131-138 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 707137-2 1978 In intact, sensitive cells, 6 mM NaF had no effect on glycolysis, whereas in homogenates, from both resistant and sensitive cells, lactate production was blocked by 6 mM NaF, indicating the cell membrane to be a barrier to fluoride. Fluorides 223-231 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 684703-0 1978 [Discontinuing NAF-drugs oral morphine and peteridine/preparations--tablets from digitalis leaves]. Morphine 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 278984-1 1978 The mechanism of activation of adenylate cyclase by guanylyl-5"-imidodiphosphate [Gpp(NH)p] and NaF has been investigated by studying the reconstitution of Gpp(NH)p and NaF sensitivity of an enzyme rendered insensitive to these agents by differential detergent extraction of a particulate brain enzyme. guanylyl-5"-imidodiphosphate 52-80 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 278984-1 1978 The mechanism of activation of adenylate cyclase by guanylyl-5"-imidodiphosphate [Gpp(NH)p] and NaF has been investigated by studying the reconstitution of Gpp(NH)p and NaF sensitivity of an enzyme rendered insensitive to these agents by differential detergent extraction of a particulate brain enzyme. Guanylyl Imidodiphosphate 82-90 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 25551-3 1978 NaF, at 1 and 5 mM, progressively increased this parameter while norepinephrine caused a similar effect at 10(-3) but not at 10(-6) M. Phentolamine (1 mM) blocked the stimulatory action of TSH; propranolol and atropine did not. Thyrotropin 189-192 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 25551-3 1978 NaF, at 1 and 5 mM, progressively increased this parameter while norepinephrine caused a similar effect at 10(-3) but not at 10(-6) M. Phentolamine (1 mM) blocked the stimulatory action of TSH; propranolol and atropine did not. Propranolol 194-205 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 25551-3 1978 NaF, at 1 and 5 mM, progressively increased this parameter while norepinephrine caused a similar effect at 10(-3) but not at 10(-6) M. Phentolamine (1 mM) blocked the stimulatory action of TSH; propranolol and atropine did not. Atropine 210-218 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 208916-0 1978 The relationship between contractile tension and intracellular cyclic AMP level in frog atrium: an analysis by using NaF, verapamil and ouabain. Cyclic AMP 63-73 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 274261-4 1978 The highest initial fluoride concentration was achieved with NaF (pH 4.0) and Na3FeF6 in combination with NaF, CaF2 and MgF2 (pH 4.0) whereas the greatest stability was reached with NaF. Fluorides 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 274261-4 1978 The highest initial fluoride concentration was achieved with NaF (pH 4.0) and Na3FeF6 in combination with NaF, CaF2 and MgF2 (pH 4.0) whereas the greatest stability was reached with NaF. Fluorides 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 274261-4 1978 The highest initial fluoride concentration was achieved with NaF (pH 4.0) and Na3FeF6 in combination with NaF, CaF2 and MgF2 (pH 4.0) whereas the greatest stability was reached with NaF. Fluorides 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 623787-1 1978 At a temperature just above the collagen denaturation point the aluminium walls of the pans used in microcalorimetric measurements react exothermically with NaF in test solutions. Aluminum 64-73 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 624406-0 1978 The monovalent anions chloride and azide as potent activators of NaF- and p(NH)ppG-stimulation of pancreatic adenylate cyclase. Chlorides 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 624406-0 1978 The monovalent anions chloride and azide as potent activators of NaF- and p(NH)ppG-stimulation of pancreatic adenylate cyclase. Azides 35-40 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 738539-6 1978 Since basal, NaF- and guanylyl-imidodiphosphate-stimulated enzyme activities were also affected by this compound, we may conclude that RMI 12330 A is a non-specific inhibitor of the human colonic adenylate cyclase system. RMI 12330A 135-146 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 269079-2 1977 It was shown that the fluoride concentration was highest when NaF was administered. Fluorides 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 412926-2 1977 NaF in CO2-free solutions increased the rates of calcium and phosphate uptake during remineralization. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 7-10 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 412926-2 1977 NaF in CO2-free solutions increased the rates of calcium and phosphate uptake during remineralization. Calcium 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 412926-2 1977 NaF in CO2-free solutions increased the rates of calcium and phosphate uptake during remineralization. Phosphates 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 412926-3 1977 Bicarbonate in NaF-free solutions caused small increases of calcium and phosphate uptake. Bicarbonates 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 412926-3 1977 Bicarbonate in NaF-free solutions caused small increases of calcium and phosphate uptake. Calcium 60-67 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 412926-3 1977 Bicarbonate in NaF-free solutions caused small increases of calcium and phosphate uptake. Phosphates 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 412926-4 1977 Bicarbonate with NaF in solutions synergistically increased calcium uptake, but did not affect phosphate uptake. Bicarbonates 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 412926-4 1977 Bicarbonate with NaF in solutions synergistically increased calcium uptake, but did not affect phosphate uptake. Calcium 60-67 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 199608-2 1977 Two relatively specific inhibitors of glycolysis (iodoacetate [IA], and sodium fluoride [NaF]) and a sulfhydryl-binding agent (N-ethylmaleimide [NEM] markedly inhibited phagocytosis and reduced cell deformability. Sodium Fluoride 72-87 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 272381-1 1977 Upon exposure to laser radiation, enamel powder mixed with NaF underwent an increase in crystallite size and/or perfection with a significant uptake of fluoride. Fluorides 152-160 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 272381-2 1977 Incisor teeth lased in the presence of NaF released significantly less calcium and phosphorus into sodium acetate (pH 4.0) compared with unlased controls, suggesting a possible role for the laser in caries prevention. Calcium 71-78 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 272381-2 1977 Incisor teeth lased in the presence of NaF released significantly less calcium and phosphorus into sodium acetate (pH 4.0) compared with unlased controls, suggesting a possible role for the laser in caries prevention. Phosphorus 83-93 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 272381-2 1977 Incisor teeth lased in the presence of NaF released significantly less calcium and phosphorus into sodium acetate (pH 4.0) compared with unlased controls, suggesting a possible role for the laser in caries prevention. Sodium Acetate 99-113 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 910903-5 1977 The intake of about 10 mg fluoride per day, given as NaF, resulted in a two- to threefold increase of the urinary and fecal fluoride excretion. Fluorides 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 910903-5 1977 The intake of about 10 mg fluoride per day, given as NaF, resulted in a two- to threefold increase of the urinary and fecal fluoride excretion. Fluorides 124-132 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 603776-5 1977 A histiocytic lymphoma cell line was strongly esterase positive with naphtol AS-D acetate esterase inhibited by NaF. naphtol 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 890460-5 1977 After restoration of uptake with SMP the amino acid uptake was resistant to NaF, but was markedly more sensitive to arsenite and oligomycin. smp 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 303821-4 1977 A 15 minutes incubation produced a similar effect as that observed in winter (32.8% P less than 0.05) A 15 minutes maintenance of muscles in a weak solution of NaF while increasing their resistance to the inhibitor was found to decrease their resistance to an injurious ethanol solution (3.48 M), and to 36 degrees, by 58 and 53%, respectively. Ethanol 270-277 C-X-C motif chemokine ligand 8 Homo sapiens 160-163 196990-2 1977 Clofibrate reduced basal as well as hormone-NaF)stimulated adenylate cyclase activities to about the same extent (45% inhibition at 1 mg/ml clofibrate). Clofibrate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 873155-1 1977 The adenylate cyclase system of human fundic gastric mucosa was found to respond to histamine, prostaglandin E 2 and the non-hormonal activators NaF and 5"-guanylyl-imidodiphosphate (GMP(PNP)). 4-nitrophenol 187-190 C-X-C motif chemokine ligand 8 Homo sapiens 145-148 873155-6 1977 NaF and GMP(PNP) by inducing an about 3.5-fold increase of enzyme activity were more potent in stimulating the human enzyme system than histamine and prostaglandin E 2. 4-nitrophenol 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 873155-6 1977 NaF and GMP(PNP) by inducing an about 3.5-fold increase of enzyme activity were more potent in stimulating the human enzyme system than histamine and prostaglandin E 2. Histamine 136-145 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 873155-6 1977 NaF and GMP(PNP) by inducing an about 3.5-fold increase of enzyme activity were more potent in stimulating the human enzyme system than histamine and prostaglandin E 2. Dinoprostone 150-167 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 18332-3 1977 To demonstrate fluorine availability at the enamel surface daily profiles of fluorine concentration in the saliva of seven subjects after a single administration of a NaF and Na3FeF6 tablet are presented and their effect on the remineralization of the dental enamel described. Fluorine 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 186585-8 1976 Dithiobisnitrobenzoic acid and alloxan, inhibitors of adenylate cyclase, impaired neuromuscular transmission and prevented the effects of NaF, but they did not change the responses to dibutyryl cAMP. Dithionitrobenzoic Acid 0-26 C-X-C motif chemokine ligand 8 Homo sapiens 138-141 836841-4 1977 Carnitine uptake is suppressed 90% by NaF (24MM). Carnitine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 189821-2 1977 The glycolysis inhibitors, NaF and monoiodoacetate, inhibited epinephrine or theophylline-stimulated lipolysis and parallely reduced the intracellular cyclic AMP and ATP levels; however, neither NaF nor monoidoacetate significantly affected dibutyryl cyclic AMP-induced lipolysis. Epinephrine 62-73 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 189821-2 1977 The glycolysis inhibitors, NaF and monoiodoacetate, inhibited epinephrine or theophylline-stimulated lipolysis and parallely reduced the intracellular cyclic AMP and ATP levels; however, neither NaF nor monoidoacetate significantly affected dibutyryl cyclic AMP-induced lipolysis. Theophylline 77-89 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 189821-2 1977 The glycolysis inhibitors, NaF and monoiodoacetate, inhibited epinephrine or theophylline-stimulated lipolysis and parallely reduced the intracellular cyclic AMP and ATP levels; however, neither NaF nor monoidoacetate significantly affected dibutyryl cyclic AMP-induced lipolysis. Cyclic AMP 151-161 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 189821-2 1977 The glycolysis inhibitors, NaF and monoiodoacetate, inhibited epinephrine or theophylline-stimulated lipolysis and parallely reduced the intracellular cyclic AMP and ATP levels; however, neither NaF nor monoidoacetate significantly affected dibutyryl cyclic AMP-induced lipolysis. Adenosine Triphosphate 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 189821-2 1977 The glycolysis inhibitors, NaF and monoiodoacetate, inhibited epinephrine or theophylline-stimulated lipolysis and parallely reduced the intracellular cyclic AMP and ATP levels; however, neither NaF nor monoidoacetate significantly affected dibutyryl cyclic AMP-induced lipolysis. monoidoacetate 203-217 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 189821-2 1977 The glycolysis inhibitors, NaF and monoiodoacetate, inhibited epinephrine or theophylline-stimulated lipolysis and parallely reduced the intracellular cyclic AMP and ATP levels; however, neither NaF nor monoidoacetate significantly affected dibutyryl cyclic AMP-induced lipolysis. dibutyryl 241-250 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 189821-2 1977 The glycolysis inhibitors, NaF and monoiodoacetate, inhibited epinephrine or theophylline-stimulated lipolysis and parallely reduced the intracellular cyclic AMP and ATP levels; however, neither NaF nor monoidoacetate significantly affected dibutyryl cyclic AMP-induced lipolysis. Cyclic AMP 251-261 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 1000801-2 1976 The most commonly used preservative, NaF, makes analysis of other serum constituents such as sodium and calcium and urea difficult or impossible, an especially serious limitation when sample size must be restricted. Sodium 93-99 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 1000801-2 1976 The most commonly used preservative, NaF, makes analysis of other serum constituents such as sodium and calcium and urea difficult or impossible, an especially serious limitation when sample size must be restricted. Calcium 104-111 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 1000801-2 1976 The most commonly used preservative, NaF, makes analysis of other serum constituents such as sodium and calcium and urea difficult or impossible, an especially serious limitation when sample size must be restricted. Urea 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 186585-8 1976 Dithiobisnitrobenzoic acid and alloxan, inhibitors of adenylate cyclase, impaired neuromuscular transmission and prevented the effects of NaF, but they did not change the responses to dibutyryl cAMP. Alloxan 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 138-141 1024309-5 1976 A study of non-specificity of the adaptive effect of low alcohol decreased their resistance to 0.12 M NaF by 33.3% (P less than 0.05) The same concentration of ethyl alcohol applied for periods from 15 mintes to 2 hours either caused no change or decreased significantly the resistance of muscle tissue to the temperature 36 degrees C. This effect of decrease in resistance was even more significant when the resistance to 38 degrees C was challenged. Alcohols 57-64 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 1004515-6 1976 Continuous treatment of the cells with 10(-3) M NaF had no effect on [3H]TdR labelling or mitotic indices in otherwise untreated cultures, but led to an impressive effect on DNA synthesis in Trenimon-treated cultures, without a considerable effect on the mitotic indices. Triaziquone 191-199 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 1067316-1 1976 The acid resistance of powdered human dentin increased linearly after pretreatments in 2.5, 25, 250, and 1,000 mM NaF in water. Water 121-126 C-X-C motif chemokine ligand 8 Homo sapiens 114-117 1068502-4 1976 The F uptake by enamel surfaces from 0.25 mM NaF in 175 mM NaCl, corresponding to a dish prepared with salt containing 500 parts/106 F, was about 80% greater than from the same NaF concentration in water. Sodium Chloride 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 10891-13 1976 Inorganic salts (e.g. NaCl, KCl, LiBr, NaF) produced inhibition of particulate enzyme; the degree of inhibition of Triton X-100-stimulated activity was less than that of unstimulated activity. inorganic salts 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 10891-13 1976 Inorganic salts (e.g. NaCl, KCl, LiBr, NaF) produced inhibition of particulate enzyme; the degree of inhibition of Triton X-100-stimulated activity was less than that of unstimulated activity. Octoxynol 115-127 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 184132-1 1976 The data obtained in this in vitro study indicate that contact with pit and fissure sealants to which NaF has been added in amounts ranging from 2 to 5% substantially increases the fluoride content of the enamel and reduces its solubility in acid. Fluorides 181-189 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 822869-6 1976 Inhibition of reinitiation with NaF or poly (AUG) reduced the rate of amino acid polymerization by 45% but the aldosterone to control ratio remained significantly high. Aldosterone 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 1068502-4 1976 The F uptake by enamel surfaces from 0.25 mM NaF in 175 mM NaCl, corresponding to a dish prepared with salt containing 500 parts/106 F, was about 80% greater than from the same NaF concentration in water. Salts 103-107 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 179579-2 1976 This enzymatic activity is strongly stimulated by NaF and 5"-guanylimidodiphosphate, is slightly stimulated by epinephrine, norepinephrine, isoproterenol, and prostaglandin E1 and is inhibited by calcium. Calcium 196-203 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 179579-2 1976 This enzymatic activity is strongly stimulated by NaF and 5"-guanylimidodiphosphate, is slightly stimulated by epinephrine, norepinephrine, isoproterenol, and prostaglandin E1 and is inhibited by calcium. Epinephrine 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 179579-2 1976 This enzymatic activity is strongly stimulated by NaF and 5"-guanylimidodiphosphate, is slightly stimulated by epinephrine, norepinephrine, isoproterenol, and prostaglandin E1 and is inhibited by calcium. Norepinephrine 124-138 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 1225875-5 1975 Prerinsing with sodium lauryl sulfate or cetylaminechloride annihilated the F clearance superiority of cetylaminefluoride over NaF. cetylaminechloride 41-59 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 179579-2 1976 This enzymatic activity is strongly stimulated by NaF and 5"-guanylimidodiphosphate, is slightly stimulated by epinephrine, norepinephrine, isoproterenol, and prostaglandin E1 and is inhibited by calcium. Isoproterenol 140-153 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 179579-2 1976 This enzymatic activity is strongly stimulated by NaF and 5"-guanylimidodiphosphate, is slightly stimulated by epinephrine, norepinephrine, isoproterenol, and prostaglandin E1 and is inhibited by calcium. Alprostadil 159-175 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 1062433-0 1976 Floride uptake by root dentin after immersion in 2% NaF solution with iontophoresis. floride 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 1225875-4 1975 Fluoride clearance was significantly slower after cetylaminefluoride rinses than after NaF rinses. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 1225875-5 1975 Prerinsing with sodium lauryl sulfate or cetylaminechloride annihilated the F clearance superiority of cetylaminefluoride over NaF. Sodium Dodecyl Sulfate 16-37 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 1032054-2 1976 Administration of NaF, NaCl, and mammalian calcitonin resulted in varying degree of hypolcalcaemia and hyperphosphataemia, whereas hypercalcaemia and hypophosphataemia developed during CaCl2 treatment. Calcium Chloride 185-190 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1067527-9 1976 The highest F-uptake was observed when a fluoride varnish, Duraphat (5% NaF) was applied three times at one weeks" interval. Fluorides 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 1067527-9 1976 The highest F-uptake was observed when a fluoride varnish, Duraphat (5% NaF) was applied three times at one weeks" interval. sodium fluoride topical preparation 59-67 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 1029317-0 1976 [Serum fluoride level in the NaF treatment of osteoporosis]. Fluorides 7-15 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 5277704-0 1970 The fluoride uptake by the enamel of human teeth "in vitro" after immersion in 2 per cent NaF solution with iontophoresis. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 167852-7 1975 The data is rationalized by the postulation of two independent enzyme components in brain cortex: one component is about six-fold activated by NaF and the NaF effect is enhanced by low concentrations of Ca2+ and Mg2+. magnesium ion 212-216 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 167852-10 1975 On this basis, Triton X-100 treatment results in about a three-fold increase in specific activity of the Ca2+ dependent cyclase component but a complete abolition of the NaF stimulated component. Octoxynol 15-27 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 238919-1 1975 A new telemetric system was used to determine, simultaneously, plaque pH and salivary fluoride when sucrose-containing fluoride tablets of 0.25 mg and 1.0 mg NaF were dissolved in the oral cavity. Sucrose 100-107 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 165496-3 1975 In 5-fluorouracil and 5-chlorouracil, however, the halogen is evidently abstracted by the Na to form NaF or NaC1 and the neutral uracil radical. Fluorouracil 3-17 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 165496-3 1975 In 5-fluorouracil and 5-chlorouracil, however, the halogen is evidently abstracted by the Na to form NaF or NaC1 and the neutral uracil radical. 5-chlorouracil 22-36 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 165496-3 1975 In 5-fluorouracil and 5-chlorouracil, however, the halogen is evidently abstracted by the Na to form NaF or NaC1 and the neutral uracil radical. Halogens 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 4703037-0 1973 The effects of 0.05 to 5.0 mM NaF on calcium phosphate mineral accretion and subsequent acid dissolution at enamel surfaces. calcium phosphate 37-54 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 5284490-0 1971 [Fluoride excretion in urine following administration of NaF and CaF 2 tablets]. Fluorides 1-9 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 5277132-0 1971 A method for in vitro studies of enamel fluoride uptake in single tooth surfaces with reference to NaF, NaF-H3PO4 and Na2SnF6. Fluorides 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 5458884-1 1970 Tablets of prednisolone-promethazine 40mg--25mg NAF]. prednisolone-promethazine 11-36 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 235523-3 1975 The 32P labeling of this component increased several fold when NaF was included in the incubation medium. Phosphorus-32 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 4202670-12 1974 Blood collected in EDTA-47 mM NaF had a stable, reproducible UBBC with no significant in vitro increment with time.EDTA-NaF UBBC was 640+/-168 (range 380-921 pg B(12) bound/ml plasma) for 12 normal adult men and 809+/-232 (range 505-1208) for normal adult women. ubbc 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 4202670-12 1974 Blood collected in EDTA-47 mM NaF had a stable, reproducible UBBC with no significant in vitro increment with time.EDTA-NaF UBBC was 640+/-168 (range 380-921 pg B(12) bound/ml plasma) for 12 normal adult men and 809+/-232 (range 505-1208) for normal adult women. ubbc 124-128 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 4641417-6 1972 Inhibition of triglyceride hydrolysis was observed when postheparin plasma was preincubated in 2 m NaCl, 10(-4) m protamine, 10 mm Na(4)P(2)O(7), and 0.1 m NaF. Triglycerides 14-26 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 4322665-12 1971 The activity was increased by NaF and by prostaglandin PGE(1) and was decreased by epinephrine. Epinephrine 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 5501055-14 1970 Following an 18-164 min perfusion period with 300 mM-NaF, the delayed K currents with 300 mM-KF were reduced in amplitude to less than one-tenth the initial level. lysylphenylalanine 93-95 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 5501055-18 1970 In axons perfused with 300 mM-KF, following removal of the delayed rectifier by 300 mM-NaF, the ratio of steady-state Na current: peak Na current was estimated to be about half the value obtained with NaF. lysylphenylalanine 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 5501055-18 1970 In axons perfused with 300 mM-KF, following removal of the delayed rectifier by 300 mM-NaF, the ratio of steady-state Na current: peak Na current was estimated to be about half the value obtained with NaF. lysylphenylalanine 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 201-204 5229987-0 1966 NaF inhibition of the initial binding of aminoacyl-sRNA to reticulocyte ribosomes. aminoacyl-srna 41-55 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 4237373-0 1968 ATP protection of myometrial adenosinetriphosphatase from the inhibitory effects of n-ethyl maleimide, urea and NaF. Adenosine Triphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 5982419-0 1966 [Behavior of calcemia, phosphoremia, calciuria, phosphaturia and alkaline phosphatase in normal subjects treated with sodium fluoride (NaF)]. Sodium Fluoride 118-133 C-X-C motif chemokine ligand 8 Homo sapiens 135-138 14238892-0 1964 REACTIONS OF NAF AND SNF2 WITH DENTAL ENAMEL HAVING VARYING CA:P RATIOS. Phosphorus 63-64 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 13563565-2 1958 The division of cell potassium into two fractions during incubation with 0.025 M NaF. Potassium 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 33581669-3 2021 This study aimed at exploring the role of sodium or other fluorides (NaF), which are intentionally added to flux-cored wire electrodes for stainless steel welding, on the solubility (in phosphate buffered saline) and toxicity of the generated welding fume particles. Sodium 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 13245009-0 1955 [Acid solubility and fluorine content of dental enamel treated with NaF under different conditions; preliminary report]. Fluorine 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 33581669-3 2021 This study aimed at exploring the role of sodium or other fluorides (NaF), which are intentionally added to flux-cored wire electrodes for stainless steel welding, on the solubility (in phosphate buffered saline) and toxicity of the generated welding fume particles. Fluorides 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 33581669-3 2021 This study aimed at exploring the role of sodium or other fluorides (NaF), which are intentionally added to flux-cored wire electrodes for stainless steel welding, on the solubility (in phosphate buffered saline) and toxicity of the generated welding fume particles. Phosphate-Buffered Saline 186-211 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 33848541-10 2021 In contrast, the non-pairing of the Ibuprofen:Colistin and Ibuprofen:Tadim combinations showed a significant decrease in IL-8 secretion at both the concentrations. Ibuprofen 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 33848541-10 2021 In contrast, the non-pairing of the Ibuprofen:Colistin and Ibuprofen:Tadim combinations showed a significant decrease in IL-8 secretion at both the concentrations. Ibuprofen 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 33581669-6 2021 The welding fume particles containing NaF released significantly higher amounts of Cr(VI) compared with solid wire reference fumes, which was associated with increased cytotoxicity and genotoxicity in-vitro. chromium hexavalent ion 83-89 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 33848541-10 2021 In contrast, the non-pairing of the Ibuprofen:Colistin and Ibuprofen:Tadim combinations showed a significant decrease in IL-8 secretion at both the concentrations. tadim 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 33982762-3 2021 The results of ELISA and reverse transcription-quantitative PCR revealed that THCA reduced the secretion and mRNA expression levels of interleukin (IL)-6; IL-8; thymus and activation-regulated chemokine; macrophage-derived chemokine; regulated upon activation, normal T cell expressed and secreted; and monocyte chemoattractant protein-1 in TI mixture-stimulated HaCaT cells. thca 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 33781846-11 2021 After independent confirmation, poly(I:C)-EVs upregulated BMP6 (p = 0.035) and flagellin-EVs upregulated CXCL8 (p = 0.005), VEGFA (p = 0.018) and PTGS2 (p = 0.020) compared to control-EVs. flagellin-evs 79-92 C-X-C motif chemokine ligand 8 Homo sapiens 105-110 33934954-2 2021 In the current meta-analysis, we attempted to clarify the efficacy of curcumin/turmeric supplementation in reducing concentrations of interleukin (IL)-1, IL-6, IL-8, and tumor necrosis factor (TNF)-alpha in patients with an inflammatory background. Curcumin 70-78 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 33934954-3 2021 The main databases were searched to identify eligible trials evaluating the effect of curcumin in reducing IL-1, IL-6, IL-8, and TNF-alpha in serum up to March 2021. Curcumin 86-94 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 33934954-7 2021 Nonetheless, curcumin/turmeric supplementation was non-significantly associated with reduced levels of IL-6 (WMD = -0.33 pg/ml, 95% CI = -0.99-0.34, P = 0.33) and increased levels of IL-8 (WMD = 0.52 pg/ml, 95% CI = -1.13-2.17, P = 0.53). Curcumin 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 33934954-8 2021 The dose-responses analysis indicated that curcumin/turmeric supplementation resulted in IL-1 and IL-8 alteration in a non-linear model. Curcumin 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 33683746-9 2021 Indeed, palmitate, a major free fatty acid with elevated plasma levels in diabetic patients, induced the expression of inflammatory cytokines found in the ocular fluid of DR patients such as CXCL8 (IL-8) and ANGPTL4. Palmitates 8-17 C-X-C motif chemokine ligand 8 Homo sapiens 191-196 33683746-9 2021 Indeed, palmitate, a major free fatty acid with elevated plasma levels in diabetic patients, induced the expression of inflammatory cytokines found in the ocular fluid of DR patients such as CXCL8 (IL-8) and ANGPTL4. Palmitates 8-17 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 33683746-10 2021 Moreover, the analysis of palmitate-treated hiMGC secretome showed an upregulation of proangiogenic factors strongly related to DR, including ANG2, Endoglin, IL-1beta, CXCL8, MMP-9, PDGF-AA, and VEGF. Palmitates 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 168-173 33930649-11 2021 The green tea extract and EGCG also had a dose-dependent inhibitory effect on irinotecan-induced secretion of interleukin-6 and interleukin-8 by oral epithelial cells. epigallocatechin gallate 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 33895548-5 2021 Exogenous 17beta-estradiol (E2) stimulated endothelial exocytosis of Weibel-Palade bodies (WPBs), releasing von Willebrand factor (vWF) and interleukin-8 (IL-8). Estradiol 10-26 C-X-C motif chemokine ligand 8 Homo sapiens 140-153 33895548-5 2021 Exogenous 17beta-estradiol (E2) stimulated endothelial exocytosis of Weibel-Palade bodies (WPBs), releasing von Willebrand factor (vWF) and interleukin-8 (IL-8). Estradiol 10-26 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 33895548-5 2021 Exogenous 17beta-estradiol (E2) stimulated endothelial exocytosis of Weibel-Palade bodies (WPBs), releasing von Willebrand factor (vWF) and interleukin-8 (IL-8). Estradiol 28-30 C-X-C motif chemokine ligand 8 Homo sapiens 140-153 33895548-5 2021 Exogenous 17beta-estradiol (E2) stimulated endothelial exocytosis of Weibel-Palade bodies (WPBs), releasing von Willebrand factor (vWF) and interleukin-8 (IL-8). Estradiol 28-30 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 33930649-11 2021 The green tea extract and EGCG also had a dose-dependent inhibitory effect on irinotecan-induced secretion of interleukin-6 and interleukin-8 by oral epithelial cells. Irinotecan 78-88 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 33350460-6 2021 RESULTS: Among the 30 samples, the mean decrease in glucose levels was highest in the SSJ tube (0.38 mmol/L), followed by 0.16 mmol/L in Na citrate tube and 0.14 mmol/L in NaF-KOx tube. Glucose 52-59 C-X-C motif chemokine ligand 8 Homo sapiens 172-175 33781652-0 2021 Glycosaminoglycans located on neutrophils and monocytes impact on CXCL8- and CCL2-induced cell migration. Glycosaminoglycans 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 66-71 33781652-4 2021 Subsequent analysis of CXCL8- and CCL2-induced chemotaxis revealed that leukocyte migration was strongly reduced after eliminating heparan sulfate from the surface of neutrophils and monocytes. Heparitin Sulfate 131-146 C-X-C motif chemokine ligand 8 Homo sapiens 23-28 33604932-0 2021 The role of IL-8 in skin lesions of a patient with erythema elevatum diutinum. diutinum 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 33857626-2 2021 Although induction of death receptor-initiated extrinsic apoptosis by sodium fluoride (NaF) has been reported, its mechanism of action is still not clearly defined. Sodium Fluoride 70-85 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 33857626-7 2021 Notably, we demonstrated that NaF could induce a significant increase in intracellular reactive oxygen species (ROS) level derived from nicotinamide adenine dinucleotide phosphate oxidase 4 (NOX4). Reactive Oxygen Species 87-110 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 33857626-7 2021 Notably, we demonstrated that NaF could induce a significant increase in intracellular reactive oxygen species (ROS) level derived from nicotinamide adenine dinucleotide phosphate oxidase 4 (NOX4). Reactive Oxygen Species 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 33857626-8 2021 Specifically, NOX4 knockdown inhibited NaF-induced the activation of p53/DR5 axis by reducing NOX4-derived ROS production. Reactive Oxygen Species 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 33857626-9 2021 Further in vivo investigation demonstrated that NOX4 deficiency markedly attenuates NaF-induced lung injury, apoptosis, and ROS levels in the lung. Reactive Oxygen Species 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 33677254-0 2021 Tumor-associated macrophages-mediated CXCL8 infiltration enhances breast cancer metastasis: Suppression by Danirixin. danirixin 107-116 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 33677254-6 2021 Then, we showed that TAMs-released CXCL8 could markedly elevate the migration, invasion and EMT events in breast cancer cells, as well as the self-renewal of BCSCs in vitro. tams 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 33677254-8 2021 Consistently, the in vivo analysis confirmed that CXCL8 suppression using Danirixin effectively reduced the tumor growth, lung metastasis and repressed the self-renewal of BCSCs. danirixin 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 33677254-9 2021 Collectively, TAMs/CXCL8 could enhance BCSCs self-renewal and breast cancer metastasis, and these effects could be markedly abolished by Danirixin treatment, suppressing breast cancer progression consequently. danirixin 137-146 C-X-C motif chemokine ligand 8 Homo sapiens 19-24 34036759-0 2021 Loading of capsaicin-in-cyclodextrin inclusion complexes into PEGylated liposomes and the inhibitory effect on IL-8 production by MDA-MB-231 and A549 cancer cell lines. capsaicin-in-cyclodextrin 11-36 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 33830449-0 2021 Ellagitannins from Rosa roxburghii suppress poly(I:C)-induced IL-8 production in human keratinocytes. Hydrolyzable Tannins 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 33830449-0 2021 Ellagitannins from Rosa roxburghii suppress poly(I:C)-induced IL-8 production in human keratinocytes. Poly I-C 44-53 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 33830449-2 2021 The RRFE inhibited interleukin-8 (IL-8) mRNA expression in normal human epidermal keratinocytes (NHEKs) stimulated with polyinosinic:polycytidylic acid (poly(I:C)), a ligand of toll-like receptor-3 (TLR-3). polyinosinic 120-132 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 33830449-2 2021 The RRFE inhibited interleukin-8 (IL-8) mRNA expression in normal human epidermal keratinocytes (NHEKs) stimulated with polyinosinic:polycytidylic acid (poly(I:C)), a ligand of toll-like receptor-3 (TLR-3). polyinosinic 120-132 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 33830449-4 2021 The purified compounds, strictinin and casuarictin, inhibited the IL-8 mRNA expression and IL-8 release induced in NHEKs by poly(I:C). strictinin 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 33830449-4 2021 The purified compounds, strictinin and casuarictin, inhibited the IL-8 mRNA expression and IL-8 release induced in NHEKs by poly(I:C). strictinin 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 33639259-1 2021 OBJECTIVE: Molecular information derived from dynamic [18F]sodium fluoride ([18F]NaF) PET imaging holds promise as a quantitative marker of bone metabolism. [18f]sodium fluoride 54-74 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 33843989-12 2021 Therefore, in a high-glucose environment, IL-8 activated the Akt signaling pathway, promoted paracrine mechanisms of BMSCs, and improved the proliferation and migration of HUVECs. Glucose 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 33830449-4 2021 The purified compounds, strictinin and casuarictin, inhibited the IL-8 mRNA expression and IL-8 release induced in NHEKs by poly(I:C). casuarictin 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 33830449-4 2021 The purified compounds, strictinin and casuarictin, inhibited the IL-8 mRNA expression and IL-8 release induced in NHEKs by poly(I:C). casuarictin 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 33830449-4 2021 The purified compounds, strictinin and casuarictin, inhibited the IL-8 mRNA expression and IL-8 release induced in NHEKs by poly(I:C). Poly I-C 124-133 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 33830449-4 2021 The purified compounds, strictinin and casuarictin, inhibited the IL-8 mRNA expression and IL-8 release induced in NHEKs by poly(I:C). Poly I-C 124-133 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 33846813-8 2021 Furthermore, the results also revealed a decrease in IL1B-induced IL8, MMP-1, and MMP-9 expression in response to celastrol treatment. celastrol 114-123 C-X-C motif chemokine ligand 8 Homo sapiens 66-69 34057209-11 2021 Long-term exposure of HGFs to nicotine or CSC significantly suppressed their cellular proliferation and migration and upregulated type I collagen, type III collagen, interleukin (IL)-6, IL-8, p16, p21, and p53 mRNA expression, and IL-6 and IL-8 protein expression. Nicotine 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 34057209-11 2021 Long-term exposure of HGFs to nicotine or CSC significantly suppressed their cellular proliferation and migration and upregulated type I collagen, type III collagen, interleukin (IL)-6, IL-8, p16, p21, and p53 mRNA expression, and IL-6 and IL-8 protein expression. Nicotine 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 240-244 34050537-5 2022 Particles comprising high copper (Cu) and zinc (Zn) content activated human endothelial cells via a non-ROS-mediated mechanism that triggered immune activation (IL-8, GM-CSF), leukocyte adhesion to the endothelium (soluble intercellular adhesion molecule 1 (sICAM-1)), and secretion of regulators of the acute-phase protein synthesis (interleukin 6 (IL-6)). Copper 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 34050537-5 2022 Particles comprising high copper (Cu) and zinc (Zn) content activated human endothelial cells via a non-ROS-mediated mechanism that triggered immune activation (IL-8, GM-CSF), leukocyte adhesion to the endothelium (soluble intercellular adhesion molecule 1 (sICAM-1)), and secretion of regulators of the acute-phase protein synthesis (interleukin 6 (IL-6)). Zinc 48-50 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 34033222-2 2021 We investigated whether use of reparixin for blockade of the CXCL8 pathway would improve islet engraftment and insulin independence after TPIAT. reparixin 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 61-66 33689220-3 2021 Herein, a low-cost 19 m (m: mol kg -1) bi-salts WISE with a wide ESW of 2.8 V was designed, where the low-cost 17 m NaClO4 extends the anodic limiting potential to 4.4 V, while the fluorine-containing salt (2 m NaOTF) extends the cathodic limiting potential to 1.6 V by forming a NaF-Na2O-NaOH SEI on anodes. bi-salts 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 280-283 34030480-9 2021 Moreover, Poly(I:C)-HMW/LyoVec and Poly(I:C)-HMW were the only ligands that significantly increased IL-8 secretion. Poly I-C 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 34030480-10 2021 Interestingly, HBV infection reduced IL-8 secretion induced by Poly(I:C)-HMW and to a lesser extent Poly(I:C)-HMW/LyoVec. Poly I-C 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 34006909-9 2021 The integration of metabolic and immune data indicated a molecular signature constituted by IL-6, IL1-ra, DMG, CCL4, Ile, Gly and IL-8, which could discriminate patients and healthy subjects and could represent a candidate tool in the diagnosis of new-onset psoriasis. dimethylglycine 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 34018029-11 2021 Among patients with IRRs, those receiving ibrutinib-obinutuzumab had lower post-obinutuzumab increases in IL-6, IL-8, IL-10, and MCP-1 (P < 0.04) than patients receiving chlorambucil-obinutuzumab. ibrutinib 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 34020271-3 2021 Our previous work has confirmed that premature senescent hepatocytes induced by Cr(VI) expressed high level of Clusterin (CLU) and secrete interleukin-6 (IL-6) and IL-8. chromium hexavalent ion 80-86 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 34020271-5 2021 In this study we demonstrated that Cr(VI) induced the secretion of tumor promoting components of SASP such as IL-6, IL-8, and granulocyte-macrophage colony stimulating factor (GM-CSF) in senescent L-02 hepatocytes, while the levels of the anti-tumor components of SASP such as chemokine (c-x-c motif) ligand-1 (CXCL-1) and monocyte chemoattractant protein-1 (MCP-1) were not altered. chromium hexavalent ion 35-41 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 34020271-7 2021 The NF-kappaB inhibitor PDTC significantly alleviated Cr(VI)-induced increase of IL-6, IL-8, and GM-CSF, confirming that NF-kappaB can regulate the tumor promoting components of SASP. prolinedithiocarbamate 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 34020271-7 2021 The NF-kappaB inhibitor PDTC significantly alleviated Cr(VI)-induced increase of IL-6, IL-8, and GM-CSF, confirming that NF-kappaB can regulate the tumor promoting components of SASP. chromium hexavalent ion 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 34001091-8 2021 Time course studies showed that ORMDL3-deficient A549 and NHBE cells had an attenuated IL-6 and IL-8 response to poly I:C stimulation. Poly I-C 113-121 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 33689220-3 2021 Herein, a low-cost 19 m (m: mol kg -1) bi-salts WISE with a wide ESW of 2.8 V was designed, where the low-cost 17 m NaClO4 extends the anodic limiting potential to 4.4 V, while the fluorine-containing salt (2 m NaOTF) extends the cathodic limiting potential to 1.6 V by forming a NaF-Na2O-NaOH SEI on anodes. sodium perchlorate 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 280-283 33993290-9 2021 The A2B agonist BAY60-6583 significantly elevated levels of IL6 and CXCL8, a result also obtained with adenosine and its analogue NECA. BAY 60-6583 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 68-73 33989405-6 2021 Conditions of 60 mM glucose potentiated secretion of the cytokine IL-8 suggesting that cytokine secretion during hyperglycemia may be a source of tissue inflammation. Glucose 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 33675827-7 2021 The loading of LVOX into CH/ZA induced its anti-inflammatory effect against the cytokine production (IL-6 and IL-8) within the human bronchial epithelia cells (NL20). Levofloxacin 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 33989405-7 2021 TNFalpha measurably increased secretion of IL-8 and IL-1beta, which was enhanced at 60 mM glucose. Glucose 90-97 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 34007158-9 2021 FTY720 reduced the secretion of IL-1beta, IL-6, and IL-8 from TNF-alpha-stimulated MH7A cells in a dose-dependent manner. Fingolimod Hydrochloride 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 33990437-8 2021 PSB reduced postoperative inflammatory response by limiting concentrations of proinflammatory cytokines IL-8, IL-18, IL-23, IL-33 and MCP-1 measured in the first 7-day after surgery (p<0.05). psb 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 33958662-6 2021 Both epoxygenated fatty acids significantly decreased IL-8 expression in IL-1beta-induced MC and TNFalpha in PA-induced MC. epoxygenated fatty acids 5-29 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 34040530-15 2021 Upstream regulators of cathine and cathinone were found to potentially target several molecules including interleukin-8, MMP2, PLAU, and micro-RNAs. norpseudoephedrine 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 106-119 34040530-15 2021 Upstream regulators of cathine and cathinone were found to potentially target several molecules including interleukin-8, MMP2, PLAU, and micro-RNAs. cathinone 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 106-119 33964033-13 2021 Fluvastatin reduced IL8, IL6, CCL21, AQP9 (p<0.001) and MMP9 (p<0.05) in the ex-vivo pulpitis model, while dequalinium chloride reduced AQP9 (p<0.001) but had no significant effect on the other biomarkers. Fluvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 33960079-3 2021 Among them, GCP-1 (Cycle-(Trp-Glu-His-Thr)) inhibited proliferation and induced human cervical cancer (HeLa) cells apoptosis and blocked the HeLa cells in G0/G1 phase significantly. Tryptophan 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 12-17 33960079-3 2021 Among them, GCP-1 (Cycle-(Trp-Glu-His-Thr)) inhibited proliferation and induced human cervical cancer (HeLa) cells apoptosis and blocked the HeLa cells in G0/G1 phase significantly. Glu-His 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 12-17 33960079-3 2021 Among them, GCP-1 (Cycle-(Trp-Glu-His-Thr)) inhibited proliferation and induced human cervical cancer (HeLa) cells apoptosis and blocked the HeLa cells in G0/G1 phase significantly. Threonine 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 12-17 33960079-5 2021 Moreover, GCP-1 suppressed the cyclin expression and activated the caspase cascade and poly(ADP-ribose) polymerase. Poly Adenosine Diphosphate Ribose 87-103 C-X-C motif chemokine ligand 8 Homo sapiens 10-15 33950330-1 2021 To examine 2-year changes in carotid and aortic 18F-sodium fluoride (NaF) uptake in both healthy controls and angina pectoris patients. 18f-sodium fluoride 48-67 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 33949204-8 2021 p55PIK deficiency and TAT-N15 significantly inhibited the cigarette smoke extract-induced IL-6, IL-8, and activation of the Akt and the NF-kappaB pathway in BEAS-2B. tat-n15 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 33421881-6 2021 The levels of interleukin (IL)-1beta, IL-6, IL-8 and IL-13 were about 1.5 times higher in the PFOA-treated A549 and L-02 cells than in the controls. perfluorooctanoic acid 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 33421881-8 2021 Arginine and vitamin B6 supplemented into cell culture effectively decreased the levels of IL-6 and IL-8. Arginine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 33421881-8 2021 Arginine and vitamin B6 supplemented into cell culture effectively decreased the levels of IL-6 and IL-8. Vitamin B 6 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 33947432-0 2021 Correction to: Genistein inhibits stemness of SKOV3 cells induced by macrophages co-cultured with ovarian cancer stem-like cells through IL-8/STAT3 axis. Genistein 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 32697835-6 2021 E2 levels were negatively correlated with IL-2R, IL-6, IL-8 and TNFalpha in luteal phase (Pearson Correlation=-0.592, -0.558, -0.545, -0.623; p=0.033, 0.048, 0.054, 0.023), and with C3 in follicular phase (Pearson Correlation=-0.651; p=0.030). Estradiol 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 33484111-6 2021 MP and SP groups were significantly different in terms of IL8, IL10 and sSELE levels. 6-trimethylsilylthio-9-trimethylsilylpurine 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 33947407-12 2021 DISCUSSION: Our study revealed elevated plasma levels of inflammatory mediators in different PAH subgroups and CTEPH at baseline and at 1-year follow-up, whereby CXCL9 and IL-8 may prove to be prognostic markers for CTEPH patients. cteph 216-221 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 33484111-6 2021 MP and SP groups were significantly different in terms of IL8, IL10 and sSELE levels. sp 7-9 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 33550164-7 2021 We found that TNF-alpha, IL-1beta, IL-6, and IL-8 were the four immune mediators that elevated in most of the samples derived from patients with CP/CPPS and the EAP models. phosphorylethanolamine 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 33222241-4 2021 RESULTS: Levels of IL-16, CXCL8, CXCL10, CCL17, and CCL22 were significantly increased in reactions (1+, 2+) to thiurams and fragrances compared to their petrolatum controls, except for PT reactions to FM I/II with negative breakdown testing in which, however, decreased levels of NMF were observed. Thiram 112-120 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 33144047-10 2021 On the contrary, RHE treated with PM or TS after preconditioning by a semi-dry airflow show a lower increase in IL-1alpha, IL-8, and RANTES compared to preconditioning by a humid airflow. Promethium 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 33176493-8 2021 Besides, we found correlations of interleukin-8 with age, glucose, and lipid profile in the overfat group. Glucose 58-65 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 33091430-8 2021 In contrast, bisphenols significantly reduced the production of CXCL8/IL-8 by neutrophils, an effect found to be greater with the glucuronidated metabolites. bis(4-hydroxyphenyl)sulfone 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 64-69 33091430-8 2021 In contrast, bisphenols significantly reduced the production of CXCL8/IL-8 by neutrophils, an effect found to be greater with the glucuronidated metabolites. bis(4-hydroxyphenyl)sulfone 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 33747166-6 2021 In comparison with the control group, patients in the Dex group exhibited a significant increase in cardiac function, as indicated by an increase in HR, MAP and IL-10 levels, and a significant decrease in cTnI, IL-8, MDA and glucose levels. Dexmedetomidine 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 33649784-11 2021 The pharmacological induction of autophagy with rapamycin or metformin attenuated the pro-migratory effects of IL-8. Sirolimus 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 33649784-11 2021 The pharmacological induction of autophagy with rapamycin or metformin attenuated the pro-migratory effects of IL-8. Metformin 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 33649784-12 2021 Neutralizing anti-IL-8 antibody counteracted the inhibitory effect of OVCAF-CM on basal autophagy. ovcaf-cm 70-78 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 33596158-0 2021 l-Cysteine Stimulates the Effect of Vitamin D on Inhibition of Oxidative Stress, IL-8, and MCP-1 Secretion in High Glucose Treated Monocytes. Cysteine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 31914352-9 2021 There was significant positive correlation between serum vitamin D and Th1 cytokines IL-2 and IL-8 as well as Th2 cytokines (ILs-3, 4, 5 and 9), but negative correlation with IL-13Conclusions: Serum Vitamin D and cytokines were lower in a sample of Nigerian children with asthma than controls. Vitamin D 57-66 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 33596158-0 2021 l-Cysteine Stimulates the Effect of Vitamin D on Inhibition of Oxidative Stress, IL-8, and MCP-1 Secretion in High Glucose Treated Monocytes. Vitamin D 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 33596158-3 2021 This study examined the hypothesis that supplementation with vitamin D, in combination with l-cysteine (LC), is better at reducing oxidative stress and thereby, more effective, at inhibiting the secretion of the pro-inflammatory cytokines, Interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1) in U937 monocytes exposed to high glucose concentrations. Vitamin D 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 240-253 33596158-3 2021 This study examined the hypothesis that supplementation with vitamin D, in combination with l-cysteine (LC), is better at reducing oxidative stress and thereby, more effective, at inhibiting the secretion of the pro-inflammatory cytokines, Interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1) in U937 monocytes exposed to high glucose concentrations. Vitamin D 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 255-259 33596158-3 2021 This study examined the hypothesis that supplementation with vitamin D, in combination with l-cysteine (LC), is better at reducing oxidative stress and thereby, more effective, at inhibiting the secretion of the pro-inflammatory cytokines, Interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1) in U937 monocytes exposed to high glucose concentrations. Cysteine 104-106 C-X-C motif chemokine ligand 8 Homo sapiens 240-253 33596158-3 2021 This study examined the hypothesis that supplementation with vitamin D, in combination with l-cysteine (LC), is better at reducing oxidative stress and thereby, more effective, at inhibiting the secretion of the pro-inflammatory cytokines, Interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1) in U937 monocytes exposed to high glucose concentrations. Cysteine 104-106 C-X-C motif chemokine ligand 8 Homo sapiens 255-259 33219895-8 2021 Furthermore, we detected elevated levels of IL-8, IL-6, and TNF-alpha in EH patients could activate platelets/ECs and induce elevated PS exposure on their membranes. Phosphatidylserines 134-136 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 33711406-1 2021 OBJECTIVE: To examine the biochemical components of multi-species biofilm on the arginine (Arg)-sodium fluoride (NaF) varnish-treated enamel following bacterial pH-cycling. Arginine 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 33711406-1 2021 OBJECTIVE: To examine the biochemical components of multi-species biofilm on the arginine (Arg)-sodium fluoride (NaF) varnish-treated enamel following bacterial pH-cycling. Arginine 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 33711406-1 2021 OBJECTIVE: To examine the biochemical components of multi-species biofilm on the arginine (Arg)-sodium fluoride (NaF) varnish-treated enamel following bacterial pH-cycling. Sodium Fluoride 96-111 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 33711406-4 2021 The experimental and control groups were: 1%, 2%, 4% Arg-NaF, NaF, and no treatment. Arginine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 33711406-8 2021 RESULTS: The total carbohydrate content of the biofilm was the lowest for the 2% and 4% Arg-NaF (p < 0.05). Carbohydrates 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 33711406-8 2021 RESULTS: The total carbohydrate content of the biofilm was the lowest for the 2% and 4% Arg-NaF (p < 0.05). Arginine 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 33711406-9 2021 Except for 2% Arg-NaF, the biofilm proteins for 4% Arg-NaF were significantly higher than the other groups (p < 0.05). Arginine 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 33711406-9 2021 Except for 2% Arg-NaF, the biofilm proteins for 4% Arg-NaF were significantly higher than the other groups (p < 0.05). Arginine 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 33711406-10 2021 The amyloids for Arg-NaF groups were significantly lower than the controls (p < 0.05). Arginine 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 33711406-11 2021 The eDNA for 4% Arg-NaF was significantly higher than the controls (p < 0.05). Arginine 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 33711406-12 2021 The 2% and 4% Arg-NaF-treated enamel had increased biofilm Pi and F compared to the NaF-treated enamel (p < 0.05). Arginine 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 33711406-13 2021 The proportion of biofilm EPS matrix to bacteria was significantly reduced in Arg-NaF groups compared to the controls (p < 0.05). eps 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 33711406-13 2021 The proportion of biofilm EPS matrix to bacteria was significantly reduced in Arg-NaF groups compared to the controls (p < 0.05). Arginine 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 33711406-14 2021 The dead bacterial proportions of 4% Arg-NaF were significantly higher than the controls (p < 0.05). Arginine 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 33711406-15 2021 CONCLUSION: Higher concentrations (i.e. 2%/4%) of Arg in 5% NaF varnish have the potential to modulate the biochemical composition of the biofilm growing on the treated enamel. Arginine 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 33760117-11 2021 Inhibition of CXCL8 in combination with miR-302c-3p and/or miR-520a-3p overexpression exerted proliferation-suppressive and apoptosis-stimulating effects on CC cells, whereas restoring CXCL8 attenuated the miR-302c-3p- and miR-520a-3p-induced anti-proliferative and pro-apoptotic effects. mir-302c-3p 206-217 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 33632872-2 2021 Surprisingly though, DCs cultured in the presence of supernatant derived from VPA-treated cancer cells showed a reduced allostimulatory capacity and an increased release of IL-10 and IL-8 cytokines in comparison to those exposed to TSA-treated cells culture supernatant. Valproic Acid 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 33760162-0 2021 Escin inhibits angiogenesis by suppressing interleukin-8 and vascular endothelial growth factor production by blocking nuclear factor-kappaB activation in pancreatic cancer cell lines. Escin 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 43-56 33576698-7 2021 ZnO NPs delivered at 1.0 microg/cm2 in the NACIVT system, mimicking occupational exposure, induced significant increases in metabolic activity and release of the cytokines IL-8 and MCP-1, but no differences were observed using traditional exposures. Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 33576698-7 2021 ZnO NPs delivered at 1.0 microg/cm2 in the NACIVT system, mimicking occupational exposure, induced significant increases in metabolic activity and release of the cytokines IL-8 and MCP-1, but no differences were observed using traditional exposures. nacivt 43-49 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 33760162-8 2021 Furthermore, ELISA confirmed that NF-kappaB activity in the escin-treated PaCa cells was significantly inhibited and reverse transcription-quantitative PCR showed that the mRNA expression levels of tumor necrosis factor-alpha-induced IL-8 and VEGF were significantly suppressed following escin treatment in the PaCa cell lines. Escin 288-293 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 34033999-0 2021 Sulforaphane inhibits the expression of interleukin-6 and interleukin-8 induced in bronchial epithelial IB3-1 cells by exposure to the SARS-CoV-2 Spike protein. sulforaphane 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 34035660-8 2021 Results: In IL-1beta-primed cells, preincubation with Vanillin reduced IL-6, IL-8, COX-2, and iNOS expression and NO release, compared to IL-1beta-primed cells. vanillin 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 34035660-10 2021 Furthermore, in presence of mechanical injury, the Vanillin preincubation, wound closure may be reducing the expression and release of IL-6 and TNF-alpha and upregulation of COX-2 and IL-8. vanillin 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 33760162-9 2021 ELISA also showed that escin decreased the secretion of IL-8 and VEGF from the PaCa cells. Escin 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 33760162-8 2021 Furthermore, ELISA confirmed that NF-kappaB activity in the escin-treated PaCa cells was significantly inhibited and reverse transcription-quantitative PCR showed that the mRNA expression levels of tumor necrosis factor-alpha-induced IL-8 and VEGF were significantly suppressed following escin treatment in the PaCa cell lines. Escin 60-65 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 33760162-11 2021 These results indicated that escin inhibited angiogenesis by reducing the secretion of IL-8 and VEGF by blocking NF-kappaB activity in PaCa. Escin 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 33893805-5 2022 To one of the aliquots sodium fluoride (NaF, 1% w/v) was added. Sodium Fluoride 23-38 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 33984751-10 2021 Interaction network construction and topological analysis yielded 60 hub targets, of which 18 were major hub targets, among which IL-6, IL-8, TNF, PI3K, MAPK, and NF-kappaB (RELA) are the most important in LYT"s treatment of AAD-induced MetS. L-2-Aminoadipic acid 225-228 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 33876932-0 2021 Kosmotropic Electrolyte (Na2CO3, NaF) Perturbs the Air/Water Interface through Anion Hydration Shell without Forming a Well-Defined Electric Double Layer. Water 55-60 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 33876932-2 2021 By combining heterodyne-detected vibrational sum frequency generation (HD-VSFG) with differential spectroscopy involving simultaneous curve fitting (DS-SCF) analysis, we retrieve electrolyte (Na2CO3 and NaF)-correlated OH-stretch spectra of water at the air/water interface. Water 241-246 C-X-C motif chemokine ligand 8 Homo sapiens 203-206 33876932-2 2021 By combining heterodyne-detected vibrational sum frequency generation (HD-VSFG) with differential spectroscopy involving simultaneous curve fitting (DS-SCF) analysis, we retrieve electrolyte (Na2CO3 and NaF)-correlated OH-stretch spectra of water at the air/water interface. Water 258-263 C-X-C motif chemokine ligand 8 Homo sapiens 203-206 33987174-6 2021 More specifically, chloroquine elution down-regulates interleukin 8 (IL-8) and matrix metalloproteinase nine secretion while up-regulating hepatocyte growth factor, vascular endothelial growth factor A, and IL-22 secretion, suggesting a potential shift toward a resolving neutrophil phenotype. Chloroquine 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 33987174-6 2021 More specifically, chloroquine elution down-regulates interleukin 8 (IL-8) and matrix metalloproteinase nine secretion while up-regulating hepatocyte growth factor, vascular endothelial growth factor A, and IL-22 secretion, suggesting a potential shift toward a resolving neutrophil phenotype. Chloroquine 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 33899586-9 2021 Interestingly; the over expression of Nrf2 using Nrf2-Ad-WT or Sulforaphane was also associated with significant upregulation of IL-8 compared to controls. sulforaphane 63-75 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 33913531-1 2021 The aim of this study was to assess the modulatory effect of TcpA in the expression of CEACAM1 adhesin molecule and IL-1, IL-8 and TNFalpha pro-inflammatiory cytokines in the co-culture model of Caco-2/PBMC that can mimic the intestinal milieu. chlorfenac 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 33913531-9 2021 In conclusion, V.cholerae TcpA induces statistically significant dose-dependent stimulatory effect on TNFalpha, IL-1 and IL-8 pro-inflammatory cytokines expression. chlorfenac 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 33900421-4 2021 IL6-174 GC and IL8-251 T allele showed a protective effect in women against ACG development and, conversely, IL8-251 polymorphism showed a risk for men. acg 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 33923126-1 2021 ACRIN 6687, a multi-center clinical trial evaluating differential response of bone metastases to dasatinib in men with metastatic castration-resistant prostate cancer (mCRPC), used [18F]-fluoride (NaF) PET imaging. acrin 6687 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 197-200 33923126-8 2021 Pharmacodynamic changes with dasatinib in tumor bone can be identified by WB NaF PET in men with mCRPC. Dasatinib 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 33903806-7 2021 In the case of GCF, taurine levels were positively correlated with IL-8 levels in both groups (all P < 0.05). Taurine 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 33893193-1 2022 Coronary 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) and computed tomography (CT) angiography-based quantitative plaque analysis have shown promise in refining risk stratification in patients with coronary artery disease. 18f-sodium fluoride 9-28 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 33900308-6 2021 Syringic acid and kuromanin, standard compounds found in FBBBR, significantly decreased the interleukin (IL)-1beta, IL-6 and IL-8 levels in PM2.5-treated HaCaT cells. syringic acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 33919366-2 2021 The current study addressed the question of how palmitate might interact with insulin or PGE2 to induce the formation of the chemotactic pro-inflammatory cytokine interleukin-8 (IL-8). Palmitates 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 163-176 33919366-2 2021 The current study addressed the question of how palmitate might interact with insulin or PGE2 to induce the formation of the chemotactic pro-inflammatory cytokine interleukin-8 (IL-8). Palmitates 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 33919366-0 2021 Enhanced Palmitate-Induced Interleukin-8 Formation in Human Macrophages by Insulin or Prostaglandin E2. Palmitates 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 33919366-0 2021 Enhanced Palmitate-Induced Interleukin-8 Formation in Human Macrophages by Insulin or Prostaglandin E2. Dinoprostone 86-102 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 33919366-2 2021 The current study addressed the question of how palmitate might interact with insulin or PGE2 to induce the formation of the chemotactic pro-inflammatory cytokine interleukin-8 (IL-8). Dinoprostone 89-93 C-X-C motif chemokine ligand 8 Homo sapiens 163-176 33900308-6 2021 Syringic acid and kuromanin, standard compounds found in FBBBR, significantly decreased the interleukin (IL)-1beta, IL-6 and IL-8 levels in PM2.5-treated HaCaT cells. cyanidin 3-O-glucopyranoside 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 33919366-2 2021 The current study addressed the question of how palmitate might interact with insulin or PGE2 to induce the formation of the chemotactic pro-inflammatory cytokine interleukin-8 (IL-8). Dinoprostone 89-93 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 33919366-4 2021 In these macrophages, palmitate induced IL-8 formation. Palmitates 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 33919366-5 2021 Insulin enhanced the induction of IL-8 formation by palmitate as well as the palmitate-dependent stimulation of PGE2 synthesis. Palmitates 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 33850164-5 2021 Cromolyn and a new fluorinated analog dramatically reduced the secretion of a wide spectrum of inflammatory mediators, which included cytokines such as IL-1beta, IL-6, IL-8 and IFN-gamma, and chemokines such as CXCL10, CCL2, CCL3 and CCL4. Cromolyn Sodium 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 33919366-6 2021 PGE2 in turn elicited IL-8 formation on its own and enhanced the induction of IL-8 release by palmitate, most likely by activating the EP4 receptor. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 33919366-6 2021 PGE2 in turn elicited IL-8 formation on its own and enhanced the induction of IL-8 release by palmitate, most likely by activating the EP4 receptor. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 33919366-6 2021 PGE2 in turn elicited IL-8 formation on its own and enhanced the induction of IL-8 release by palmitate, most likely by activating the EP4 receptor. Palmitates 94-103 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 33919366-7 2021 Since IL-8 causes insulin resistance and fosters inflammation, the increase in palmitate-induced IL-8 formation that is caused by hyperinsulinemia and locally produced PGE2 in chronically inflamed adipose tissue might favor disease progression in a vicious feed-forward cycle. Palmitates 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 33919366-7 2021 Since IL-8 causes insulin resistance and fosters inflammation, the increase in palmitate-induced IL-8 formation that is caused by hyperinsulinemia and locally produced PGE2 in chronically inflamed adipose tissue might favor disease progression in a vicious feed-forward cycle. Palmitates 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 33919366-7 2021 Since IL-8 causes insulin resistance and fosters inflammation, the increase in palmitate-induced IL-8 formation that is caused by hyperinsulinemia and locally produced PGE2 in chronically inflamed adipose tissue might favor disease progression in a vicious feed-forward cycle. Dinoprostone 168-172 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 33882577-8 2021 A concentration-dependent significant increase in pro-inflammatory markers C-C motif chemokine ligand 2, interleukin (IL)6, and IL8 was observed for EB-exposed A549 cells compared to CA. ethylbenzene 149-151 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 33959001-11 2021 In MSCs, atorvastatin and aspirin combination reduced the release of pro-inflammatory cytokines such as IL-6, IL-8, MCP-1 and IFN-gamma. Atorvastatin 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 33959001-11 2021 In MSCs, atorvastatin and aspirin combination reduced the release of pro-inflammatory cytokines such as IL-6, IL-8, MCP-1 and IFN-gamma. Aspirin 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 33959001-12 2021 Atorvastatin alone reduced the release of IL-6, IL-8 and MCP-1 from co-cultures of stroke monocytes and MSCs. Atorvastatin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 33921615-12 2021 In addition, lipoxin A4 inhibited the infiltration of neutrophils and the production of cytokines and pro-inflammatory chemokines, such as interleukin (Il-1beta, Il-6, Il-8) and tumor necrosis factor-alpha (TNF-alpha). lipoxin A4 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 33857948-5 2021 Using flow cytometric methods, we determined that the IL-8-induced cellular activity was largely dependent on specific ion channels and transporters, such as the sodium-proton exchanger 1 (NHE1) and non-NHE1-dependent sodium flux. Sodium 162-168 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 33857948-5 2021 Using flow cytometric methods, we determined that the IL-8-induced cellular activity was largely dependent on specific ion channels and transporters, such as the sodium-proton exchanger 1 (NHE1) and non-NHE1-dependent sodium flux. Sodium 218-224 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 33855585-9 2022 CONCLUSION: IL-6 and IL-8 baseline values predicted outcomes of sorafenib-treated patients in this well-characterized prospective cohort of the SORAMIC trial. Sorafenib 64-73 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 33854135-6 2021 We did find evidence of an increase in IL-8 production by epithelial cells with increasing bioavailable iron (p = 0.01), however, this was not linked to the pyrite content of the coal (p = 0.75) and we did not see any evidence of a positive association in the other cell types. Iron 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 33887366-8 2021 Our findings demonstrated that these specific non-traditional biomarkers measured together with more conventional ones (e.g., CDT, EtG, IL8, ALT, AST, GGT) could represent novel key parameters for monitoring alcohol use disorders and withdrawal being also suggestive of the complexity of psychoneuroimmune response to alcohol. Alcohols 208-215 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 33860869-10 2021 Further experiments revealed that S1-induced increase in the production of TNFalpha, IL-6, IL-1beta and IL-8 was reduced in the presence of BAY11-7082 and SKF 86002, while CRID3 pre-treatment resulted in the reduction of IL-1beta production. 3-(4-methylphenylsulfonyl)-2-propenenitrile 140-150 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 33860869-10 2021 Further experiments revealed that S1-induced increase in the production of TNFalpha, IL-6, IL-1beta and IL-8 was reduced in the presence of BAY11-7082 and SKF 86002, while CRID3 pre-treatment resulted in the reduction of IL-1beta production. 6-(4-fluorophenyl)-2,3-dihydro-5-(4-pyridinyl)imidazo(2,1-b)thiazole 155-164 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 33860562-0 2021 5-Aminolaevulinic acid photodynamic therapy amplifies intense inflammatory response in the treatment of acne vulgaris via CXCL8. Aminolevulinic Acid 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 33860562-6 2021 Besides, ALA-PDT could up-regulate the expression of CXCL8 in vivo and in vitro, amplifying the inflammatory response by recruiting T cells, B cells, neutrophils and macrophages. Alanine 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 53-58 33860562-7 2021 We also found that ALA-PDT elevated the expression of CXCL8 via p38 pathway. Alanine 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 54-59 33860562-8 2021 SB203580, a p38 pathway inhibitor, decreased the expression of CXCL8 in sebocytes after ALA-PDT. SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 63-68 33860562-8 2021 SB203580, a p38 pathway inhibitor, decreased the expression of CXCL8 in sebocytes after ALA-PDT. Alanine 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 63-68 33860562-9 2021 These findings indicate that ALA-PDT amplifies the intense inflammatory response in treatment of acne vulgaris via CXCL8. Alanine 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 115-120 33937285-5 2021 Among such class of drugs, azithromycin is described as azalide and is well-known for its ability to decrease the production of pro-inflammatory cytokines, including matrix metalloproteinases, tumor necrosis factor-alpha, interleukin (IL)-6, and IL-8. Azithromycin 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 33937285-5 2021 Among such class of drugs, azithromycin is described as azalide and is well-known for its ability to decrease the production of pro-inflammatory cytokines, including matrix metalloproteinases, tumor necrosis factor-alpha, interleukin (IL)-6, and IL-8. azalide 56-63 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 32865318-12 2021 Isorhamnetin significantly decreased the expression of interleukin (IL)-1beta, IL-6, IL-8, and C-X-C motif chemokine ligand 10 in BEAS-2B cells induced by TNF-alpha. 3-methylquercetin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 33921194-4 2021 In vitro decitabine administration increased bacterial phagocytosis and IL-8 release, but impaired microbicidal activity of monocytes. Decitabine 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 33846374-9 2021 DEHP exposure led to a proinflammatory state in SGBS-derived adipocytes (e.g., increased secretion of IL8 and MCP1). Diethylhexyl Phthalate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 33508282-9 2021 However, a prolonged exposure with each of the antihistamines impaires the increase in COX-2 and IL-8 mRNA levels induced by histamine, even after ligand removal. Histamine 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 33481051-6 2021 A significant release of IL-8 was found after 72 h of exposure to 2.5 mug/cm2 BCDPs. bcdps 78-83 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 33210765-13 2021 LTA-stimulated DPSCs released IL-6 and IL-8 in a dose-dependent manner (P <= 0.0001). lipoteichoic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 33021119-0 2021 Pyrvinium pamoate induces in-vitro suppression of IL-6 and IL-8 produced by human endometriotic stromal cells. pyrvinium 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 33021119-7 2021 Our Findings showed that pyrvinium pamoate suppresses the mRNA gene expression and secretion of IL-6 and IL-8 in human endometriotic stromal cells. pyrvinium 25-42 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 33834669-9 2021 Sitagliptin suppressed 5 microg mL-1 of LPS-induced IL-6, IL-8, CCL2, and SOD2 gene expression levels in HGF in a concentration-dependent manner. Sitagliptin Phosphate 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 33834669-10 2021 Furthermore, sitagliptin significantly decreased the elevated secretion of IL-6, IL-8, and CCL2 protein induced by LPS. Sitagliptin Phosphate 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 33834669-12 2021 Results of qRT-PCR analysis indicated that 0.5 micromol L-1 of sitagliptin and 5 micromol L-1 of BAY11-7082 significantly inhibited LPS-induced IL-6, IL-8, CCL2, and SOD2 gene expressions. Sitagliptin Phosphate 63-74 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 33834669-12 2021 Results of qRT-PCR analysis indicated that 0.5 micromol L-1 of sitagliptin and 5 micromol L-1 of BAY11-7082 significantly inhibited LPS-induced IL-6, IL-8, CCL2, and SOD2 gene expressions. 3-(4-methylphenylsulfonyl)-2-propenenitrile 97-107 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 33393728-3 2021 The present study was designed to characterize the mechanisms by which mangiferin protects against NaF-induced neurotoxicity. mangiferin 71-81 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 33830910-10 2021 Interleukin-8 secretion was induced in TLR4/MD2/CD14-transfected, but not in TLR2-transfected, HEK 293 T cells following TcdB or CDT exposure.Conclusion. trimethylaminocarboxyldihydroboran 121-125 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 33830910-10 2021 Interleukin-8 secretion was induced in TLR4/MD2/CD14-transfected, but not in TLR2-transfected, HEK 293 T cells following TcdB or CDT exposure.Conclusion. 1,5,9-cyclododecatriene 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 33582555-3 2021 C/EBPbeta is a leucine-zipper transcription factor that regulates expression of a variety of inflammatory cytokines or chemokines, such as IL-8, G-CSF (granulocyte colony stimulating factor), and GM-CSF (granulocyte macrophage colony stimulating factor) which induce neutrophil infiltration and differentiation. Leucine 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 33207020-6 2021 For soft tissues, agarose gels with varying concentrations of agarose, gadolinium (Gd) and sodium fluoride (NaF) were developed. Sepharose 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 32559758-7 2021 RESULTS: IL-6 and IL-8 were highly expressed in pediatric Q-CPs, and the transcription level of IL-6 was the highest in the severe group. q-cps 58-63 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 33116000-1 2021 The aim of this study was to investigate the effects of potassium fluoride (KF) and sodium fluoride (NaF) in different concentrations on micro-shear bond strength (microSBS) and their protective effects against acid. Sodium Fluoride 84-99 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 33859989-8 2021 Furthermore, the serum and urine Zn concentrations negatively correlated with the serum IL-6 and IL-8 concentrations. Zinc 33-35 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 33346953-7 2021 PAR1 activation also enhanced polyinosinic:polycytodylic acid induction of IL-8 in a human endothelial cell line. polycytodylic acid 43-61 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 33306627-1 2021 OBJECTIVES: F-sodium fluoride (NaF) is a radiotracer used in PET that reflects calcium metabolism and osteoblastic activity. f-sodium fluoride 12-29 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 33306627-1 2021 OBJECTIVES: F-sodium fluoride (NaF) is a radiotracer used in PET that reflects calcium metabolism and osteoblastic activity. Calcium 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 33849824-7 2021 Amentoflavone down-regulated the mRNA expressions of IL-6 and TNF-alpha, up-regulated mRNA expressions of IL-8 and TGF-beta mRNA (P < 0.05), and increased the protein expressions of PPAR-alpha/gamma, Arg-1 and Fizz1. amentoflavone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 33841413-7 2021 The TLR4 signaling inhibitor, TAK-242, inhibited HUVEC IL-8 secretion in response to SS plasma by 85%. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 33753826-8 2021 In addition, puerarin reduced the activities of aspartate aminotransferase and alkaline phosphatase, the ratio of serum aspartate aminotransferase to serum alanine aminotransferase, the number of white blood cells and neutrophils, and the plasma concentrations of interleukin-6, interleukin-8 and tumor necrosis factor-alpha, as well as protein abundances of heat shock protein-70 in PEDV-infected piglets. puerarin 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 279-292 33782320-8 2021 Inflammatory cytokines such as IL-1alpha, IL-8, and tumor necrosis factor-alpha were suppressed by selenium in cultured orbital fibroblasts of patients with GO. Selenium 99-107 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 33730343-12 2021 The manuscript provides evidence that the phototherapy can interfere with MAPK signaling via cAMP in order to attenuate the IL-8 secretion from CSE-stimulated BEAS. Cyclic AMP 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 33524139-7 2021 Following DAAs therapy, the levels of ROS, IL-1beta, IL-6, IL-8 and TNF-alpha were significantly decreased in the three HCV groups. daas 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 33738852-3 2021 The objective of the present study was to investigate the protective effects of glycine on sodium fluoride (NaF) exposure and the possible underlying mechanisms in a porcine testicular Sertoli cell line model. Glycine 80-87 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 33738852-3 2021 The objective of the present study was to investigate the protective effects of glycine on sodium fluoride (NaF) exposure and the possible underlying mechanisms in a porcine testicular Sertoli cell line model. Sodium Fluoride 91-106 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 33738852-4 2021 Cellular viability and proliferation were examined following NaF exposure and glycine supplementation, and glycine dramatically ameliorated the decreases in NaF-induced porcine testicular Sertoli cell viability and proliferation. Glycine 107-114 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 33738852-5 2021 Further investigations revealed that glycine decreased NaF-induced intracellular reactive oxygen species production, DNA fragment accumulation, and the apoptosis incidence in the porcine testicular Sertoli cell line; in addition, glycine improved mitochondrial function and ATP production. Glycine 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 33738852-5 2021 Further investigations revealed that glycine decreased NaF-induced intracellular reactive oxygen species production, DNA fragment accumulation, and the apoptosis incidence in the porcine testicular Sertoli cell line; in addition, glycine improved mitochondrial function and ATP production. Oxygen 90-96 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 33738852-5 2021 Further investigations revealed that glycine decreased NaF-induced intracellular reactive oxygen species production, DNA fragment accumulation, and the apoptosis incidence in the porcine testicular Sertoli cell line; in addition, glycine improved mitochondrial function and ATP production. Glycine 230-237 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 33738852-5 2021 Further investigations revealed that glycine decreased NaF-induced intracellular reactive oxygen species production, DNA fragment accumulation, and the apoptosis incidence in the porcine testicular Sertoli cell line; in addition, glycine improved mitochondrial function and ATP production. Adenosine Triphosphate 274-277 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 33738852-6 2021 Notably, results of the SPiDER-beta-Gal analysis suggested that glycine alleviated NaF-induced cellular senescence and downregulated P53, P21, HMGA2, and P16INK4a gene expression in the porcine testicular Sertoli cell line. Glycine 64-71 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 33738852-7 2021 Collectively, the beneficial effects of glycine alleviate NaF-induced oxidative stress, apoptosis and senescence, and together with our previous findings, support the hypothesis that glycine plays an important role in protecting against NaF exposure-induced impairments in the porcine testicular Sertoli cell line. Glycine 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 33738852-7 2021 Collectively, the beneficial effects of glycine alleviate NaF-induced oxidative stress, apoptosis and senescence, and together with our previous findings, support the hypothesis that glycine plays an important role in protecting against NaF exposure-induced impairments in the porcine testicular Sertoli cell line. Glycine 183-190 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 33738852-7 2021 Collectively, the beneficial effects of glycine alleviate NaF-induced oxidative stress, apoptosis and senescence, and together with our previous findings, support the hypothesis that glycine plays an important role in protecting against NaF exposure-induced impairments in the porcine testicular Sertoli cell line. Glycine 183-190 C-X-C motif chemokine ligand 8 Homo sapiens 237-240 33730343-15 2021 The dexamethasone corticoid produces a significant inhibitory effect on IL-8 as well as ROS secretion, but on the other hand, the corticoid blocked the IL-10 secretion. Dexamethasone 4-17 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 32789453-1 2021 OBJECTIVE: Sodium fluoride (NaF) has been applied to inhibit glycolysis in venous specimens for decades. Sodium Fluoride 11-26 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 33189376-7 2021 Likewise, serum Cu was positively associated with HO-1 (beta = 0.0004, P = 0.03) and negatively associated with MCP-1 (beta = -0.0006, P = 0.003) and IL-8 (beta = -0.002, P = 0.03). Copper 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 33790807-6 2021 Induction of IL-6, IL-8, and ICAM-1 synthesis from cultured PTECs incubated with IgA-HMC conditioned medium was significantly suppressed by treatment with the Syk inhibitor R406 compared to that from healthy control. R406 173-177 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 33723220-3 2021 Whether IL-8 predicts depression response to ketamine and in a sex-specific manner is not known. Ketamine 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 33710470-8 2021 CONCLUSION: Peripheral blood IL-6 and IL-8 levels could play a role in the severity of DME and UME, respectively. dme 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 33842407-0 2021 Ascorbic Acid Suppresses House Dust Mite-Induced Expression of Interleukin-8 in Human Respiratory Epithelial Cells. Ascorbic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 33842407-6 2021 The present study was aimed to investigate whether HDM could induce IL-8 expression through activation of MAPKs, NF-kappaB, and AP-1 and whether ascorbic acid could inhibit HDM-stimulated IL-8 expression by reducing ROS and suppressing activation of MAPKs, NF-kappaB, and AP-1 in respiratory epithelial H292 cells. Ascorbic Acid 145-158 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 33723220-6 2021 Baseline levels of IL-8 had a trending association with response to ketamine, depending upon sex (responder status x sex interaction: p = 0.096), in which lower baseline levels of IL-8 in females (p = 0.095) but not males (p = 0.96) trended with treatment response. Ketamine 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 33723220-6 2021 Baseline levels of IL-8 had a trending association with response to ketamine, depending upon sex (responder status x sex interaction: p = 0.096), in which lower baseline levels of IL-8 in females (p = 0.095) but not males (p = 0.96) trended with treatment response. Ketamine 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 33723275-11 2021 In particular, gossypol suppressed the expression of genes coding for CLAUDIN1, ELK1, FAS, GAPDH, IL2, IL8 and ZFAND5 mRNAs, but enhanced the expression of the gene coding for GLUT3 mRNA. Gossypol 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 33201565-12 2021 Cell experiments showed that overexpression of miR-221-5p significantly inhibited the expression of inflammatory factors tumor necrosis factor-alpha, IL-8, and IL-1beta, while down-regulation of miR-221-5p was the opposite. -221-5p 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 33567990-7 2022 Medroxyprogesterone acetate (MPA)/progesterone (P4) and IL-1beta/IL-8 treatment resulted in altered TFV-DP levels in VK2 and PM1 cells. Dipyridamole 104-106 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 33567990-8 2022 MPA and P4 at concentrations above 0.1 microM, as well as IL-1beta and IL-8 at concentrations above 10 ng/mL significantly decreased HIV-1BaL inhibition in PM1 cells when 1 microM TFV was added. Tenofovir 180-183 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 33555876-4 2021 Tests for reactive oxygen species (ROS), biomarker expressions (CYP1A1, IL8, COX-2), and mutagenicity (Ames) show that RNG exhaust has toxicity that is comparable or lower than CNG exhaust. Benzene 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 33155332-9 2021 Moreover, L-lactic acid level was positively associated with serum CXCL8 level. Lactic Acid 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 67-72 33483132-13 2021 In healthy volunteers, phenylephrine enhanced the LPS-induced IL-10 response (+76%, P=0.0008) while attenuating plasma concentrations of pro-inflammatory mediators including IL-8 (-15%, P=0.03). Phenylephrine 23-36 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 33646017-1 2021 Background: Patients with osteoblastic bone metastases are candidates for radium-223 (223RaCl2) therapy and may undergo sodium fluoride-18 (18F-NaF) positron emission tomography-computed tomography imaging to identify bone lesions. Sodium Fluoride 120-135 C-X-C motif chemokine ligand 8 Homo sapiens 144-147 33646017-2 2021 18F-NaF has been shown to predict 223RaCl2 uptake, but intratumor distributions of these two agents remain unclear. 223racl2 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 33570794-7 2021 Moreover, PARP-1 silencing and PARP inhibitor olaparib can suppress UVB-induced COX-2 and MMP-1 expression, but enhance TNF-alpha and IL-8 expression. olaparib 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 33570794-8 2021 In addition, EGFR silencing or EGFR inhibition by gefitinib can decrease UVB-induced COX-2, TNF-alpha, and IL-8 expression, suggesting EGFR activation via paracrine action can mediate UVB-induced inflammation responses. Gefitinib 50-59 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 33755043-7 2021 SNPs in the CXCL8 gene encoding IL-8 was significantly associated with protection from SICs (chr4: rs1126647, odds ratio [OR] = 0.3, P = 0.005, rs2227543, OR = 0.4, P = 0.007, and rs2227307, OR = 0.4, P = 0.02) after adjusting for age, sex, steroids prediagnosis, and herpes simplex keratitis (HSK) misdiagnosis. Steroids 241-249 C-X-C motif chemokine ligand 8 Homo sapiens 12-17 33755043-7 2021 SNPs in the CXCL8 gene encoding IL-8 was significantly associated with protection from SICs (chr4: rs1126647, odds ratio [OR] = 0.3, P = 0.005, rs2227543, OR = 0.4, P = 0.007, and rs2227307, OR = 0.4, P = 0.02) after adjusting for age, sex, steroids prediagnosis, and herpes simplex keratitis (HSK) misdiagnosis. Steroids 241-249 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 33854720-8 2021 Compared with those in the Ctrl, only ARISTIN showed a significant reduction in IL-8 level, whereas TIMP1 levels were significantly upregulated in the Lyc gel and ARISTIN sites. aristin 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 33249645-10 2021 Furthermore, significantly higher expression of the pro-inflammatory cytokines IL-6 and IL-8 is detected after FLS cells interacted with NETs which derived from neutrophils stimulated with ACPA-containing IgG antibodies. arachidonylcyclopropylamide 189-193 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 33404125-2 2021 Tumor necrosis factor (TNF)-alpha/interleukin (IL)-23/IL-17 inflammatory pathway may be involved in the pathogenesis of PPP, and the skin lesions manifest the enhanced expression of IL-8 in keratinocytes and increased levels of antimicrobial peptide cathelicidin, leucine leucine-37 in vesicles/pustules. Leucine 264-271 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 33039404-10 2021 Gene reporter assays and ChIP-PCR demonstrated that NFAT response element in its promoter played a key role in BA-induced human IL-8 expression. Bile Acids and Salts 111-113 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 33227158-1 2021 Historically, blood alcohol concentration (BAC) studies utilized a 1% concentration of the preservative sodium fluoride (NaF), leaving an information gap supporting usage of lower concentrations of NaF to preserve ethanol. Sodium Fluoride 104-119 C-X-C motif chemokine ligand 8 Homo sapiens 121-124 33653802-13 2021 BCG-induced cytokines showed a progressive increase in IL-8 (p=0.02) and TNF-alpha (p=0.04) over time for patients on rapamycin 2.0 mg, whereas patients receiving placebo had no significant change in urinary cytokines. Sirolimus 118-127 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 33142344-8 2021 Furthermore P. pubescens extract and vouacapan diterpene furan isomer"s mixture significantly decreased IL-8 levels. vouacapan diterpene furan 37-62 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 33544929-7 2021 The 18Co-CM-induced increase in CD133+CD44+ cells was attenuated by IL-6- and IL-8-neutralizing antibodies. 18co 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 30664079-9 2021 One month after intravitreal steroid injection, the IL-8 levels normalized to 13.28 pg/mL. Steroids 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 33671042-8 2021 Butyrate (0.1 mM), propionate (0.3 mM), and TSA inhibited the IL-8 production and activation of NF-kappaB. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 33671042-2 2021 The aim of this study was to investigate whether intracellular IL-33 mediates the effects of butyrate and propionate on TNFalpha-induced IL-8 production and vascular cell adhesion molecule-1 (VCAM-1) expression. Butyrates 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 33707464-8 2021 PGD2 induced IL-8 production by human group 2 innate lymphoid cells, suggesting that PGD2-producing MCs induce neutrophil recruitment into the synovium of RA patients. Prostaglandin D2 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 33707464-8 2021 PGD2 induced IL-8 production by human group 2 innate lymphoid cells, suggesting that PGD2-producing MCs induce neutrophil recruitment into the synovium of RA patients. Prostaglandin D2 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 33639877-13 2021 Eyes with FUS had significantly higher aqueous humor (AH) cytokine levels (VEGF, bFGF, IL-6, IL-8 and IL-10) compared with the control eyes (P < 0.05). fusarubin 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 33652978-8 2021 RESV cooperated with PRI-2191 in regulating the expression of IL-8 in EGFRmut cells, while OPN in KRASmut cells and PD-L1 in both cell subtypes. 1 alpha,24-dihydroxyvitamin D3 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 33671042-2 2021 The aim of this study was to investigate whether intracellular IL-33 mediates the effects of butyrate and propionate on TNFalpha-induced IL-8 production and vascular cell adhesion molecule-1 (VCAM-1) expression. Propionates 106-116 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 33671042-8 2021 Butyrate (0.1 mM), propionate (0.3 mM), and TSA inhibited the IL-8 production and activation of NF-kappaB. Propionates 19-29 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 33671042-11 2021 In conclusion, we showed that the inhibitory effects of butyrate and propionate on TNFalpha-induced IL-8 production were mediated by the HDACs/IL-33/NF-kappaB pathway, while their effects on VCAM-1 expression might be associated with the HDACs/MAPK signaling pathway, independently of IL-33. Butyrates 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 33671042-8 2021 Butyrate (0.1 mM), propionate (0.3 mM), and TSA inhibited the IL-8 production and activation of NF-kappaB. trichostatin A 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 33671042-11 2021 In conclusion, we showed that the inhibitory effects of butyrate and propionate on TNFalpha-induced IL-8 production were mediated by the HDACs/IL-33/NF-kappaB pathway, while their effects on VCAM-1 expression might be associated with the HDACs/MAPK signaling pathway, independently of IL-33. Propionates 69-79 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 33539102-2 2021 Superoxide anion species (O2-) are detected on the Pt(111) surface in an O2-saturated solution with a NaF/HClO4 mixture with pH 5.5 by the observation of a O-O vibration band at ca. superoxide anion species 0-24 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 33732225-7 2021 After infection of AGS cells, H. pylori DeltadppA induced a higher level of NF-kappaB activation and IL-8 production compared with wild-type. deltadppa 40-49 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 33600064-8 2021 The study demonstrated the ultrasound-triggered release of sodium fluorescein (NaF), bovine serum albumin (BSA), and bone morphogenetic protein 2 (BMP-2) from the hydrogels. Fluorescein 59-77 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 33708766-7 2020 Furthermore, rCdtC reduces H. pylori CagA translocation, which decreases nuclear factor kappa-B activation and interleukin-8 production, resulting in the mitigation of gastric epithelial cell inflammation. rcdtc 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 33622325-8 2021 Olodaterol reduced RSV-mediated IL-8 secretion in both COPD and control ALIs and also significantly reduced Muc5AC staining in COPD-ALIs infected with RSV. olodaterol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 33622325-10 2021 Gene silencing of the beta2-adrenergic receptor in NCI-H292 negated the ability of olodaterol to inhibit IL-8 secretion from both RSV infection and lipopolysaccharide stimulus, as did blocking of the receptor with ICI 118,551 and butaxamine. olodaterol 83-93 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 33609028-11 2021 The synthetic LXR agonist GW3965 led to a decreased nuclear positivity of the p65 subunit of nuclear factor kappa B, a phosphorylation ratio of the p44-42 MAP kinase, and the expression of CCL-28 and IL-8 in IL-1beta-stimulated Caco-2 cells. GW 3965 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 33539102-2 2021 Superoxide anion species (O2-) are detected on the Pt(111) surface in an O2-saturated solution with a NaF/HClO4 mixture with pH 5.5 by the observation of a O-O vibration band at ca. Oxygen 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 33539102-2 2021 Superoxide anion species (O2-) are detected on the Pt(111) surface in an O2-saturated solution with a NaF/HClO4 mixture with pH 5.5 by the observation of a O-O vibration band at ca. Platinum 51-53 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 33539102-2 2021 Superoxide anion species (O2-) are detected on the Pt(111) surface in an O2-saturated solution with a NaF/HClO4 mixture with pH 5.5 by the observation of a O-O vibration band at ca. Oxygen 26-28 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 33359650-5 2021 We demonstrate the ICS fluticasone propionate (FP) and two selective non-steroidal (GRT7) and steroidal (GRT10) glucocorticoid receptor (GR) agonists significantly suppress pro-inflammatory (IL-6 and IL-8) and antiviral (IFN-lambda1) cytokine production and the expression of the interferon-stimulated genes (ISGs) OAS and viperin in RV-infected bronchial epithelial cells, with a consequent increase of viral replication. Fluticasone 23-45 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 33597583-6 2021 Non-DAUs- (n = 15) showed improved brachial flow-mediated dilation (FMD) and reduced circulating IL-8, IL-12, and leptin. daus 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 33578781-5 2021 Moreover, the stimulatory effects of H2O2 on cellular senescence are associated with oxidative stress induction, such as excessive ROS production and NADPH consumption, telomere DNA damage induction, and upregulation of senescence-associated secretory phenotype factors (IL-1beta, IL-6, IL-8, COX-2, and TNF-alpha) as well as NF-kappaB activation, which were all blocked by FK866. Hydrogen Peroxide 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 287-291 33581965-10 2021 Also, the AGEs-elicited production of IL-6 and IL-8 was inhibited by Magnolol. magnolol 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 33643049-9 2021 mRNA expression of CXCL8, CYR61, FGF16 and FGFRL1 was significantly elevated by the Rb2/Rg3 treatment, and representative signaling pathways induced by these genes were found. ginsenoside Rg3 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 19-24 33643049-11 2021 The present study provides the hypothesis that SBP, via ginsenosides Rb2 and Rg3, involves the CXCR1/2 CXCL8 (IL8)-mediated PI3K/Akt and MAPK/ERK signaling pathways in achieving its proangiogenic effects. ginsenoside Rg3 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 103-108 33643049-11 2021 The present study provides the hypothesis that SBP, via ginsenosides Rb2 and Rg3, involves the CXCR1/2 CXCL8 (IL8)-mediated PI3K/Akt and MAPK/ERK signaling pathways in achieving its proangiogenic effects. ginsenoside Rg3 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 33559204-5 2021 The results showed that SiO2 stimulated the production of reactive oxygen species and malondialdehyde in the supernatant of THP-1-derived macrophages and increased the secretion of TGF-beta1, TNF-alpha, and IL-8. Silicon Dioxide 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 33644593-6 2021 In addition, feprazone prevented FFA-induced expression and secretion of proinflammatory cytokines and chemokines, such as chemokine ligand 5 (CCL5), interleukin-6 (IL-6), and interleukin-8 (IL-8). Feprazone 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 33644593-6 2021 In addition, feprazone prevented FFA-induced expression and secretion of proinflammatory cytokines and chemokines, such as chemokine ligand 5 (CCL5), interleukin-6 (IL-6), and interleukin-8 (IL-8). Feprazone 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 33562298-7 2021 However, co-treatment with TUDCA alleviated inflammatory response induced by IL-1beta, as shown by down regulation of Il-1beta, Il-6, Il-8 and Cox2, and increased the expression of antioxidant enzyme Sod2. ursodoxicoltaurine 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 33567596-6 2021 Our results showed that (i) caffeic acid targets COX-2 and its product PGE2 as well as the biosynthesis of IL-8 in the IL-1beta-treated cells and (ii) inhibits AGE formation, which could be related to (iii) the high chelating activity exerted. caffeic acid 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 33302150-5 2021 To immobilise well-controlled soluble gradients of interleukin-8 (CXCL8), an inflammatory chemokine, we developed a simple procedure using a heparin-coated PDMS-microfluidic device. Heparin 141-148 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 33539038-12 2021 According to the cytokine antibody array results, hOBs pretreated with AZA had significantly increased production of several inflammatory cytokines (P<0.05), in which the expression levels of IL-6 and IL-8 were the most dramatically increased upon LTA stimulation (P<0.01). hobs 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 33539038-12 2021 According to the cytokine antibody array results, hOBs pretreated with AZA had significantly increased production of several inflammatory cytokines (P<0.05), in which the expression levels of IL-6 and IL-8 were the most dramatically increased upon LTA stimulation (P<0.01). Decitabine 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 33539038-12 2021 According to the cytokine antibody array results, hOBs pretreated with AZA had significantly increased production of several inflammatory cytokines (P<0.05), in which the expression levels of IL-6 and IL-8 were the most dramatically increased upon LTA stimulation (P<0.01). lipoteichoic acid 248-251 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 33557291-9 2021 Solely in the open surgery group, cortisol dynamics paralleled changes in interleukin (IL)-1beta, IL-10, IL-1ra, IL-7, IL-8 and tumor necrosis factor (TNF)-alpha but did not correlate with changes in IL-6 or interferon (IFN)-gamma at any time-point. Hydrocortisone 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 33302150-5 2021 To immobilise well-controlled soluble gradients of interleukin-8 (CXCL8), an inflammatory chemokine, we developed a simple procedure using a heparin-coated PDMS-microfluidic device. Heparin 141-148 C-X-C motif chemokine ligand 8 Homo sapiens 66-71 33352397-0 2021 IL-8 exacerbates alcohol-induced fatty liver disease via the Akt/HIF-1alpha pathway in human IL-8-expressing mice. Alcohols 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 33022353-6 2021 Overexpression of duIKKalpha dramatically increased NF-kappaB activity and induced the expression of duck cytokines IFN-beta, IL-1beta, IL-6, IL-8 and RANTES in DEFs. duikkalpha 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 33352397-0 2021 IL-8 exacerbates alcohol-induced fatty liver disease via the Akt/HIF-1alpha pathway in human IL-8-expressing mice. Alcohols 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 33352397-6 2021 We found that hIL-8 can exacerbate alcohol-induced fatty liver disease via the Akt/HIF-1alpha pathway. Alcohols 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 33352397-8 2021 Moreover, hIL-8 could increase the alcohol-induced release of ROS in fatty liver caused by alcohol and exacerbate fatty liver disease. Alcohols 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 10-15 33352397-8 2021 Moreover, hIL-8 could increase the alcohol-induced release of ROS in fatty liver caused by alcohol and exacerbate fatty liver disease. Alcohols 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 10-15 33175611-11 2021 Among the inflammatory factors examined (IL-6, IL-8, IL-10, and TNF-alpha), we found that IL-8 was significantly increased after treatment with 3OC12HSL and its expression was inhibited when TLR2 was specifically blocked or silenced. N-(3-oxododecanoyl)homoserine lactone 144-152 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 33175611-11 2021 Among the inflammatory factors examined (IL-6, IL-8, IL-10, and TNF-alpha), we found that IL-8 was significantly increased after treatment with 3OC12HSL and its expression was inhibited when TLR2 was specifically blocked or silenced. N-(3-oxododecanoyl)homoserine lactone 144-152 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 33336605-10 2021 A final concentration of 9 microg/mL of azithromycin was sufficient to decrease IL-6, IL-8 mRNA, and extracellular IL-8 levels. Azithromycin 40-52 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 32725797-0 2021 Azithromycin and ciprofloxacin inhibit interleukin-8 secretion without disrupting human sinonasal epithelial integrity in vitro. Azithromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 33336605-10 2021 A final concentration of 9 microg/mL of azithromycin was sufficient to decrease IL-6, IL-8 mRNA, and extracellular IL-8 levels. Azithromycin 40-52 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 33336605-11 2021 Conclusion: Pretreatment with azithromycin decreased the expression of IL-6 and IL-8 mRNA and the release of IL-8 in bronchial epithelial cells exposed to cigarette smoke. Azithromycin 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 33336605-11 2021 Conclusion: Pretreatment with azithromycin decreased the expression of IL-6 and IL-8 mRNA and the release of IL-8 in bronchial epithelial cells exposed to cigarette smoke. Azithromycin 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 33417258-7 2021 Our data provide the first complete transcriptome for aldosterone on a human renal cell line and identifies pro-inflammatory markers (IL6, IL11, CCL7, and CXCL8) as aldosterone-repressed genes. Aldosterone 165-176 C-X-C motif chemokine ligand 8 Homo sapiens 155-160 32725797-0 2021 Azithromycin and ciprofloxacin inhibit interleukin-8 secretion without disrupting human sinonasal epithelial integrity in vitro. Ciprofloxacin 17-30 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 33499425-4 2021 The aim of the study was to verify the possibility of using [18F]F-sodium fluoride ([18F]F-NaF) and [18F]F-fluorodeoxyglucose ([18F]F-FDG) positron emission tomography/computed tomography (PET/CT) in assessing the intensity of TAVI valve degenerative processes. f-sodium fluoride 65-82 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 33300083-12 2021 The levels of interleukin-8, matrix metalloproteinase 9 and C-reactive protein were increased in the conditioned media (CM) of rGal-10-treated gingival fibroblasts. rgal-10 127-134 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 33251898-7 2021 RESULTS: Etidronate down-regulated IL-8 and MCP-1 production and NF-kappaB p65 activation induced by Pam3CSK4, but not lipid A, in U937 cells. Etidronic Acid 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 33524223-11 2021 Furthermore, ELISA experiments revealed that the SASP-CM of Dox treated cells contain inflammatory cytokines IL8 and IP10. Doxorubicin 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 33575345-4 2021 Sudachitin inhibited IL-1beta-induced IL-6, IL-8, CXC chemokine ligand (CXCL)10, CC chemokine ligand (CCL)2, MMP-1, and MMP-3 production in HPDLC. sudachitin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 33474695-2 2021 We describe aortic microcalcification activity (AMA), a novel method for quantifying 18F-sodium fluoride (18F-NaF) uptake in the thoracic aorta. 18f-sodium fluoride 85-104 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 33498195-8 2021 Indeed, it was observed that both FM and DFM decreased the IL-6, IL-8, and nitric oxide (NO) release similarly to the reference anti-inflammatory drug dexamethasone. N-ACETYL-L-PHENYLALANYL-4-[DIFLUORO(PHOSPHONO)METHYL]-L-PHENYLALANINAMIDE 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 33396024-0 2021 HER2 overexpression triggers the IL-8 to promote arsenic-induced EMT and stem cell-like phenotypes in human bladder epithelial cells. Arsenic 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 33396024-6 2021 Phosphorylation of the human epidermal growth factor receptor 2 (HER2) was key for arsenic-induced IL-8 overexpression and depended on the simultaneous activation of the MAPK, JNK, PI3K/AKT and GSK3beta signaling pathways. Arsenic 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 33396024-8 2021 These results demonstrate that the HER2/IL-8 axis is related to the acquisition of an EMT phenotype and CSCs in arsenic-treated cells. Arsenic 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 32390406-13 2021 Furthermore, astragalin reduced the level of phosphorylated IkappaBalpha and decreased the production of the inflammatory cytokines IL-6, IL-8, and TNF-alpha in the DSS-treated colon mucosa. astragalin 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 33396129-4 2021 Treatment with NPs-Nd2O3 induced an inflammatory response in human bronchial epithelial cells (16HBE) by upregulating the expression of interleukin-6 (IL-6) and interleukin-8 (IL-8). nps-nd2o3 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 33396129-4 2021 Treatment with NPs-Nd2O3 induced an inflammatory response in human bronchial epithelial cells (16HBE) by upregulating the expression of interleukin-6 (IL-6) and interleukin-8 (IL-8). nps-nd2o3 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 33396131-6 2021 This study aimed to determine the effect of sodium fluoride (NaF) on human RBC under in vitro conditions. Sodium Fluoride 44-59 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 33396131-8 2021 Treatment of RBC with NaF enhanced the generation of reactive oxygen and nitrogen species. Nitrogen 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 33396131-10 2021 NaF treatment increased the degradation of heme causing release of free iron from its porphyrin ring. Heme 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 33396131-10 2021 NaF treatment increased the degradation of heme causing release of free iron from its porphyrin ring. Iron 72-76 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 33396131-11 2021 Cellular antioxidant power was significantly decreased in NaF-treated RBC, lowering the metal reducing and free radical quenching ability of cells. Metals 88-93 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 32390406-13 2021 Furthermore, astragalin reduced the level of phosphorylated IkappaBalpha and decreased the production of the inflammatory cytokines IL-6, IL-8, and TNF-alpha in the DSS-treated colon mucosa. Dextran Sulfate 165-168 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 33746631-1 2021 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) has emerged as a promising noninvasive imaging tool for the assessment of active calcification processes in coronary artery disease. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 33431859-6 2021 As proof-of-principle, we show that inhibition of CXCL8 receptor by the small-molecule non-competitive inhibitor repertaxin attenuated the progression of UC phenotypes in vitro and in vivo. reparixin 113-123 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 33505496-2 2021 However, TACE-induced hypoxia may promote the angiogenesis and section of some cytokines, such as IL-8, and, thereby, lead to tumor metastasis. Chlorotrianisene 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 33505496-5 2021 TACE induced significant increases of neutrophil lymphocyte ratio (NLR), platelet lymphocyte ratio (PLR), IL-1beta, IL-2R, IL-6, and IL-8. Chlorotrianisene 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 33505496-9 2021 Both hypoxia and IL-8 may promote angiogenesis which was suppressed by JR. Western blot showed that IL-8 upregulated the expression of phosphorylation of AKT, ERK, NF-kappaB, and VEGFR, which were inhibited by JR. On the other hand, effects of IL-8 on the increase of p-AKT and p-ERK were also blocked by LY294002 and U0126, respectively. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 305-313 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 33505496-9 2021 Both hypoxia and IL-8 may promote angiogenesis which was suppressed by JR. Western blot showed that IL-8 upregulated the expression of phosphorylation of AKT, ERK, NF-kappaB, and VEGFR, which were inhibited by JR. On the other hand, effects of IL-8 on the increase of p-AKT and p-ERK were also blocked by LY294002 and U0126, respectively. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 305-313 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 33505496-9 2021 Both hypoxia and IL-8 may promote angiogenesis which was suppressed by JR. Western blot showed that IL-8 upregulated the expression of phosphorylation of AKT, ERK, NF-kappaB, and VEGFR, which were inhibited by JR. On the other hand, effects of IL-8 on the increase of p-AKT and p-ERK were also blocked by LY294002 and U0126, respectively. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 305-313 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 33505496-9 2021 Both hypoxia and IL-8 may promote angiogenesis which was suppressed by JR. Western blot showed that IL-8 upregulated the expression of phosphorylation of AKT, ERK, NF-kappaB, and VEGFR, which were inhibited by JR. On the other hand, effects of IL-8 on the increase of p-AKT and p-ERK were also blocked by LY294002 and U0126, respectively. U 0126 318-323 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 33505496-9 2021 Both hypoxia and IL-8 may promote angiogenesis which was suppressed by JR. Western blot showed that IL-8 upregulated the expression of phosphorylation of AKT, ERK, NF-kappaB, and VEGFR, which were inhibited by JR. On the other hand, effects of IL-8 on the increase of p-AKT and p-ERK were also blocked by LY294002 and U0126, respectively. U 0126 318-323 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 33301812-8 2021 Pretreatment of PK 11195 suppressed while AC-5216 potentiated CSM-induced apoptosis, collapse of DeltaPsim, elevation of cytoplasmic/mitochondrial ROS levels and IL-8 release. N-benzyl-N-ethyl-2-(7,8-dihydro-7-methyl-8-oxo-2-phenyl-9H-purin-9-yl)acetamide 42-49 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 32792028-6 2021 Dietary OxBC supplementation decreased the TNF-alpha and IL-8 levels in colostrum, as well as the TNF-alpha and IL-18 levels in 14-d milk. dietary oxbc 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 33521454-5 2021 Additionally, roflumilast prevented IL-18-induced expressions and secretions of pro-inflammatory cytokines such as IL-6, IL-8, and TNF-alpha. Roflumilast 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 33505496-9 2021 Both hypoxia and IL-8 may promote angiogenesis which was suppressed by JR. Western blot showed that IL-8 upregulated the expression of phosphorylation of AKT, ERK, NF-kappaB, and VEGFR, which were inhibited by JR. On the other hand, effects of IL-8 on the increase of p-AKT and p-ERK were also blocked by LY294002 and U0126, respectively. U 0126 318-323 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 33420112-5 2021 Proteomics analysis of OCT-treated skin wounds revealed significant lower levels of key players in tissue remodeling as well as reepithelization after wounding such as pro-inflammatory cytokines (IL-8, IL-6) and matrix-metalloproteinases (MMP1, MMP2, MMP3, MMP9) when compared to controls. octenidine 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 33505216-6 2021 The anti-inflammatory mechanism of GL and GA is realized via cytokines like interferon-gamma, tumor necrotizing factor-alpha, interleukin- (IL-) 1beta, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12, and IL-17. gl 35-37 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 33413425-3 2021 Different concentrations of Dex were used to attenuate the inflammation induced by IL-1beta, and its effect was assessed via RT-PCR to detect inflammatory cytokine-related mRNA levels, including those of IKbeta-alpha, IKKbeta, IL-6, IL-8, and TNF-alpha. Dexamethasone 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 33505216-6 2021 The anti-inflammatory mechanism of GL and GA is realized via cytokines like interferon-gamma, tumor necrotizing factor-alpha, interleukin- (IL-) 1beta, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12, and IL-17. Glycyrrhetinic Acid 42-44 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 33055419-7 2021 We identified fluvastatin as an inducer of galectin-7 expression by connectivity map (cMAP) analysis, confirmed this effect in keratinocytes, and demonstrated that fluvastatin attenuated IL-6 and IL-8 production induced by IL-17A. Fluvastatin 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 32763720-10 2021 Finally, NaOH and HF solutions were used to prepare high-purity NaF (>98 %) to treat the waste solutions. Sodium Hydroxide 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 32763720-10 2021 Finally, NaOH and HF solutions were used to prepare high-purity NaF (>98 %) to treat the waste solutions. Hafnium 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 33055419-7 2021 We identified fluvastatin as an inducer of galectin-7 expression by connectivity map (cMAP) analysis, confirmed this effect in keratinocytes, and demonstrated that fluvastatin attenuated IL-6 and IL-8 production induced by IL-17A. Fluvastatin 164-175 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 33389640-6 2021 RESULTS: There was a significant difference between the NaF uptake in the thoracic aorta of myeloma and HC groups [AA (myeloma = 1.82 +- 0.21, HC = 1.24 +- 0.02), AR (myeloma = 1.71 +- 0.19, HC = 1.28 +- 0.03) and DA (myeloma = 1.96 +- 0.28, HC = 1.38 +- 0.03); P-values < 0.001]. amsonic acid 214-216 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 33267660-2 2021 18F-sodium fluoride positron emission tomography (18F-NaF PET) detects early and active calcifications within the vasculature. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 33861459-7 2021 Treatment with MgSO4 results in a significant reduction in serum levels of NGAL, Hb, T.Bill, IL-6, IL-8, SNSE, S100B, EGF, PAF, CRP and IgG. Magnesium Sulfate 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 33861459-9 2021 Moreover, reduction of IL-6, IL-8, SNSE, EGF and APACHE score and increase in RASS score were significantly higher in MgSO4 group compared with placebo. Magnesium Sulfate 118-123 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 33267660-7 2021 We compared the proportion of CCS progressors in 18F-NaF PET-positive versus 18F-NaF PET-negative coronary arteries. Fluorine-18 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 33267660-11 2021 All subjects (100%, 15/15) with >=2 18F-NaF-positive coronary arteries progressed in CCS. Fluorine-18 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 33540416-13 2021 In contrast, 1,25 (OH)2 D3 pretreatment increased the production of IL-8 by LPS- and LTA-stimulated endometrial cells. Calcitriol 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 33509458-5 2021 Significantly stronger inhibition of TNF-alpha-induced IL-8 production was found in cells pre-treated with different concentrations of mixtures of BtA and the phenolic metabolites than individual compounds. Butyric Acid 147-150 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 33540416-13 2021 In contrast, 1,25 (OH)2 D3 pretreatment increased the production of IL-8 by LPS- and LTA-stimulated endometrial cells. lipoteichoic acid 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 33218942-8 2021 The expressions of TLR4/NF-kappaBp65, IL-1beta, IL-6, IL-8, and TNF-alpha significantly increased in the model group while they were down-regulated in the rebamipide pretreatment group (p < 0.05). rebamipide 155-165 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 33285354-6 2021 The highest levels of IL-1beta, IL-6, CCL2 and IL-8 were observed with MSU at 0.5 mg/ml, CPP at 0.01-0.05 mg/ml and BCP at 1 mg/ml after 18-48 h and then decreased. Uric Acid 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 33285354-6 2021 The highest levels of IL-1beta, IL-6, CCL2 and IL-8 were observed with MSU at 0.5 mg/ml, CPP at 0.01-0.05 mg/ml and BCP at 1 mg/ml after 18-48 h and then decreased. bcp 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 33866338-1 2021 OBJECTIVE: The goal of this study was to test if changes in coronary microcalcification over a two year period assessed by fluorine-18-sodium fluoride (18F-NaF) positron emission tomography/computed tomography (PET/CT) are associated with baseline subject characteristics. fluorine-18-sodium fluoride 123-150 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 32510596-1 2021 Proteasome inhibitor MG132 was shown to enhance the secretion of interleukin 8 (IL-8) by various cells. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 33390798-13 2021 Release of IL-8 into cell supernatant was increased after stimulation with suture material and was further enhanced if minor amounts of bacterial lipoteichoic acid (LTA) were added. lipoteichoic acid 146-163 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 33390798-13 2021 Release of IL-8 into cell supernatant was increased after stimulation with suture material and was further enhanced if minor amounts of bacterial lipoteichoic acid (LTA) were added. lipoteichoic acid 165-168 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 32791248-7 2021 T2 POS was positively associated with eosinophils, IgE, and FeNO, and negatively with AQLQ, sputum neutrophils, IL-17A, IL-8, and TNF-alpha. t2 pos 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 32510596-4 2021 The purpose of the present study was to explore the combinations of the AP-1 family proteins that contribute to MG132-driven IL-8 secretion. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 112-117 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 32510596-6 2021 IL-8 secretion was augmented by MG132 in both cell lines. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 32510596-12 2021 In contrast to our expectations, MG132-induced IL-8 secretion was significantly reduced in all the transfectants suggesting that other c-Jun members might form homodimers with c-Jun and contribute to IL-8 enhancement. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 33325132-0 2021 Resveratrol treatment reduces expression of MCP-1, IL-6, IL-8 and RANTES in endometriotic stromal cells. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 32510596-12 2021 In contrast to our expectations, MG132-induced IL-8 secretion was significantly reduced in all the transfectants suggesting that other c-Jun members might form homodimers with c-Jun and contribute to IL-8 enhancement. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 33325132-3 2021 In this study, we evaluated the effects of resveratrol treatment on expression of monocyte chemotactic protein-1 (MCP-1), interleukin-6 (IL-6), IL-8, and regulated upon activation, normal T cell expressed and secreted (RANTES) in endometrial stromal cells from patients with endometriosis compared with non-endometriotic controls. Resveratrol 43-54 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 33131809-11 2021 Expression of TNF and IL1B was upregulated when exposed to LPS (P < 0.001), and expression of CXCL2 and CXCL8 increased following LPS exposure with SCFA (medium x LPS; P < 0.001). Fatty Acids, Volatile 148-152 C-X-C motif chemokine ligand 8 Homo sapiens 104-109 33325132-5 2021 Resveratrol treatment significantly reduced gene and protein expression of MCP-1, IL-6, and IL-8 in EuESCs and EESCs compared with CESCs (P < .05-.001, P < .05-.001 and P < .05-<.01, respectively), and this reduction was more noticeable in EESCs than EuESCs (P < .05-<.001). Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 33325132-7 2021 Resveratrol treatment significantly reduced the expression of MCP-1, IL-6, IL-8 and RANTES in EESCs. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 33011099-12 2021 Sputum neutrophils, eosinophils, and neutrophil elastase were numerically reduced, and significant (p<0.05) reductions in IL-8 and immunoglobulin G levels occurred with lenabasum. lenabasum 169-178 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 33188848-1 2021 OBJECTIVES: To examine the enamel fluoride uptake and remineralization potential of arginine-fluoride (Arg-NaF) varnishes in a simulated clinical condition using a multi-species bacterial pH-cycling model. arginine-fluoride 84-101 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 33188848-13 2021 in a 5% NaF varnish enhanced the enamel fluoride uptake and remineralization potential of the conventional 5% NaF varnish. Fluorides 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 33188848-14 2021 CLINICAL SIGNIFICANCE: The Arg-NaF varnish addresses the limitations of fluorides on cariogenic biofilms. Fluorides 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 32866050-11 2021 In conclusion, protocol B, which applied a 25% AgNO3 solution followed by a commercially available 5% NaF varnish with fTCP semiannually, is more effective in arresting dentine caries in primary teeth as compared with protocol A, which applied a 25% AgNO3 solution followed by another commercially available 5% NaF varnish without fTCP semiannually (ClinicalTrials.gov NCT03423797). 4-Fluoro-1-(1-(2-thienyl)cyclohexyl)piperidine 119-123 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 33188848-4 2021 Experimental and control groups were: 1% Arg-NaF; 2% Arg-NaF; 4% Arg-NaF; NaF and no treatment. Arginine 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 33188848-15 2021 The Arg-NaF varnish appears a promising caries-preventive regimen that counters the pathogenic biofilms by Arg and promotes remineralization with fluorides. Arginine 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 33188848-15 2021 The Arg-NaF varnish appears a promising caries-preventive regimen that counters the pathogenic biofilms by Arg and promotes remineralization with fluorides. Arginine 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 33188848-4 2021 Experimental and control groups were: 1% Arg-NaF; 2% Arg-NaF; 4% Arg-NaF; NaF and no treatment. Arginine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 33188848-15 2021 The Arg-NaF varnish appears a promising caries-preventive regimen that counters the pathogenic biofilms by Arg and promotes remineralization with fluorides. Fluorides 146-155 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 33188848-4 2021 Experimental and control groups were: 1% Arg-NaF; 2% Arg-NaF; 4% Arg-NaF; NaF and no treatment. Arginine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 33188848-4 2021 Experimental and control groups were: 1% Arg-NaF; 2% Arg-NaF; 4% Arg-NaF; NaF and no treatment. Arginine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 33188848-4 2021 Experimental and control groups were: 1% Arg-NaF; 2% Arg-NaF; 4% Arg-NaF; NaF and no treatment. Arginine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 33188848-8 2021 RESULTS: Increasing concentrations of Arg in NaF varnish significantly increased the EFU of incipient caries-like lesions (p < 0.001). Arginine 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 33384825-2 2021 The purpose of this study was to evaluate the surface changes of resin-modified glass ionomer (RMGI) when immersed in a sodium fluoride (NaF) solution according to pH and time. Sodium Fluoride 120-135 C-X-C motif chemokine ligand 8 Homo sapiens 137-140 33140461-4 2021 The Km values of GCP1 toward H2 O2 and guaiacol were lower than GCP2. Hydrogen Peroxide 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 33188848-9 2021 The PFU for 1% Arg-NaF was significantly higher than 4% Arg-NaF and the control NaF (p < 0.05). PBMF protocol 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 33140461-4 2021 The Km values of GCP1 toward H2 O2 and guaiacol were lower than GCP2. Guaiacol 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 33140461-8 2021 Both peroxidases showed the same thermal stability range 20-50 C. GCP2 was more resistant against the effect of metal ions than GCP1. Metals 112-117 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 33140461-14 2021 Cationic peroxidase GCP1, as a natural scavenger, had high affinity toward H2 O2 coupled to oxidation of some plant phenolic compounds suggesting its role in consuming of excess H2 O2 . Hydrogen Peroxide 75-80 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 33384825-5 2021 Results: Rougher topography and increased roughness was exhibited in NaF groups, owing to the disintegration of the polysalt matrix. polysalt 116-124 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 33384825-6 2021 Reduced Sr and F was exhibited in all groups, whereas NaF group showed a decrease in Al and inorganic components. Aluminum 85-87 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 33188848-9 2021 The PFU for 1% Arg-NaF was significantly higher than 4% Arg-NaF and the control NaF (p < 0.05). Arginine 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 33140461-14 2021 Cationic peroxidase GCP1, as a natural scavenger, had high affinity toward H2 O2 coupled to oxidation of some plant phenolic compounds suggesting its role in consuming of excess H2 O2 . Hydrogen Peroxide 178-183 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 33188848-9 2021 The PFU for 1% Arg-NaF was significantly higher than 4% Arg-NaF and the control NaF (p < 0.05). Arginine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 33188848-9 2021 The PFU for 1% Arg-NaF was significantly higher than 4% Arg-NaF and the control NaF (p < 0.05). Arginine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 33188848-10 2021 Post pH-cycling, Ca/P ratio with 1%/2% Arg-NaF was closest to hydroxyapatite (1.67). Phosphorus 0-1 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 32360175-11 2021 The application of SP600125 (10 muM) significantly suppressed the induction of IL-6 and IL-8 by GroEL-treated cells. pyrazolanthrone 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 33188848-10 2021 Post pH-cycling, Ca/P ratio with 1%/2% Arg-NaF was closest to hydroxyapatite (1.67). Arginine 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 33188848-10 2021 Post pH-cycling, Ca/P ratio with 1%/2% Arg-NaF was closest to hydroxyapatite (1.67). Durapatite 62-76 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 33249629-2 2021 The anti-inflammatory potential of Naringenin-LCNs evaluated by qPCR revealed a decreased expression of IL-6, IL-8, IL-1beta, and TNF-alpha in lipopolysaccharide-induced BCi-NS1.1 cells. naringenin-lcns 35-50 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 33249629-8 2021 In addition, Naringenin-loaded LCNs efficiently reduced the levels of pro-inflammatory markers, namely, IL-1beta, IL-6, TNF-alpha, and IL-8. naringenin 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 33188848-11 2021 Mineral gain and % remineralization of 1%/2% Arg-NaF was significantly higher than the control NaF varnish (p < 0.05). Arginine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 33283480-8 2021 C-NP nanoparticles also stimulate the release of IL-lbeta, MCP-1, TNF-alpha, IL-8, IL-12p70, IL-17, IL-18, and IL-23 from MDM. c-np 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 33249629-8 2021 In addition, Naringenin-loaded LCNs efficiently reduced the levels of pro-inflammatory markers, namely, IL-1beta, IL-6, TNF-alpha, and IL-8. lcns 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 33885393-5 2021 Aim: This study aimed to evaluate the clinical effectiveness of biannual application of 38% SDF followed by 5% sodium fluoride (NaF) varnish for arresting dental caries in children and its parental acceptance. Sodium Fluoride 111-126 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 33952789-3 2021 Furthermore, fibroblasts exposed to CP-BSA, which is a model of extracellular CPs, had upregulated expression levels of mRNAs encoding matrix metalloproteinase-1 (MMP-1) and interleukin-8/CXCL8 (IL-8/CXCL8). cps 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 174-193 33952789-3 2021 Furthermore, fibroblasts exposed to CP-BSA, which is a model of extracellular CPs, had upregulated expression levels of mRNAs encoding matrix metalloproteinase-1 (MMP-1) and interleukin-8/CXCL8 (IL-8/CXCL8). cps 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 33952789-3 2021 Furthermore, fibroblasts exposed to CP-BSA, which is a model of extracellular CPs, had upregulated expression levels of mRNAs encoding matrix metalloproteinase-1 (MMP-1) and interleukin-8/CXCL8 (IL-8/CXCL8). cps 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 188-193 32294652-11 2021 RESULTS: Combined administration of vinpocetine and dexamethasone lowered the expression levels of serum inflammatory cytokines, including TLR2, TLR4, interleukin (IL)-20, IL-8, tumor necrosis factor-alpha, interferon-gamma, monocyte chemoattractant protein 2, and interferon-induced protein 20, when compared to dexamethasone monotherapy. vinpocetine 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 32294652-11 2021 RESULTS: Combined administration of vinpocetine and dexamethasone lowered the expression levels of serum inflammatory cytokines, including TLR2, TLR4, interleukin (IL)-20, IL-8, tumor necrosis factor-alpha, interferon-gamma, monocyte chemoattractant protein 2, and interferon-induced protein 20, when compared to dexamethasone monotherapy. Dexamethasone 52-65 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 33356884-6 2021 Nicaraven suppressed TNFalpha-induced mRNA expression of multiple adhesion molecules and pro-inflammatory cytokines, including VCAM-1, ICAM-1, E-selectin, MCP-1, TNFalpha, IL-1beta, IL-6 and IL-8. nicaraven 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 33491385-0 2021 Preventive effect of subacidic 1% NaF-HF gel on dental caries in 6- to 7-year-old schoolchildren: a randomized controlled trial. Hafnium 38-40 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 33396644-7 2020 In response to LPS stimulation, the gene expression levels of IL-6 and IL-8 in hGFs increased due to AZM in a concentration-dependent manner, and phosphorylation of nuclear factor kappa B (NF-kappaB) was also promoted. Azithromycin 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 33396644-10 2020 Thus, AZM may increase the expression of IL-6 and IL-8 under LPS stimulation to modify the inflammatory response and increase the expression of MMP-1 to promote connective tissue remodeling. Azithromycin 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 33371832-7 2021 Furthermore, NAC decreases TNF-alpha, IL-1beta, IL-6, IL-8, IL-10, and IL-17 serum levels in patients with sepsis, severe burns, acute liver failure, or peritoneal dialysis and may also reduce cytokine storm in COVID-19. Acetylcysteine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 33374148-2 2020 Fluorocholine-18 (FCH) and sodium fluoride-18 (NaF) have been used to assess PCa associated skeletal disease in thousands of patients by demonstrating different mechanism of uptake-cell membrane (lipid) synthesis and bone mineralization. sodium fluoride-18 27-45 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 33374148-11 2020 Total accelerated osteoblastic (bone demineralization) activity for NaF (TBA varied from 0.25 to 13.6 [kg] in M group and varied from 0.000 to 1.09 [kg] in N group. tba 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 33441226-8 2021 Interestingly, while SB203580 inhibited the activation of p38 MAPK signaling pathway, it only inhibited the mRNA levels of IL-6 and IL-8 in HDM-induced 16HBE cells, but had no effect on their protein levels. SB 203580 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 33380519-0 2021 18F-Sodium Fluoride (NaF) PET/CT in obese patients on LYSO PET/CT system: Patient dosimetry, optimization of injected activity and acquisition time. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 33380519-1 2021 Purpose: 18F-Sodium fluoride (NaF) PET/CT has a rapid single-pass extraction and fast clearance from soft tissues resulting in a better target to background ratio. 18f-sodium fluoride 9-28 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 33380519-13 2021 Patients were injected a mean activity of 215.4+-31.3 MBq with estimated mean effective absorbed doses of 4.09+-0.59mSv for 18F-NaF PET and 7.88+-1.66 mSv for CT alone. Fluorine-18 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 33614926-6 2021 Roxithromycin increased levels of IP-10 (P = .049) and decreased levels of MCP-1 (P < .001), MIP-1alpha (P < .016), ENA-78 (P < .001), and IL-8 (P < .001). Roxithromycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 33463132-9 2020 The serum concentration of IL-1beta, IL-6, and IL-8 was significantly higher in children with steroid-sensitive nephrotic syndrome (SSNS), compared with steroid-resistant nephrotic syndrome (SRNS). Steroids 94-101 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 33463132-9 2020 The serum concentration of IL-1beta, IL-6, and IL-8 was significantly higher in children with steroid-sensitive nephrotic syndrome (SSNS), compared with steroid-resistant nephrotic syndrome (SRNS). Steroids 153-160 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 33463132-11 2020 Our findings suggested the pathogenic role of pro-inflammatory cytokines in children with INS, of which IL-1beta, IL-6, and IL-8 were accurate biomarkers for the prediction of steroid response in these patients. Steroids 176-183 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 33938176-0 2021 HDAC8 promotes daunorubicin resistance of human acute myeloid leukemia cells via regulation of IL-6 and IL-8. Daunorubicin 15-27 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 32993961-11 2020 The up-regulated IL-6, IL-8, ROS, and NAPDH in the LPS-induced cells were reduced by miR-27a-3p mimic while inhibited by FOXO3. mir-27a-3p 85-95 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 33938176-7 2021 Collectively, our data suggested that HDAC8 promotes DNR resistance of human AML cells via regulation of IL-6 and IL-8. Daunorubicin 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 33339152-0 2020 Physicochemical Characteristics of Arginine Enriched NaF Varnish: An In Vitro Study. Arginine 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 33335138-5 2020 Treatment of neoplastic cells with PL alone or with annexin A1 mimic peptide reduced cell proliferation and viability and modulated the expression of MCP-1 chemokine, IL-8 cytokine and genes involved in inflammatory processes. piplartine 35-37 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 33370225-10 2022 RESULTS: In the presence of xanthine oxidase, hypoxanthine, alone and in combination with RBC supernatants, caused increases of TNF-alpha- and IL-8-positive cells after 5 hours of treatment. Hypoxanthine 46-58 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 33390996-9 2020 Amongst these index compounds a lead chemotype: 1H-pyrazolo [3,4 d] pyrimidin-4-amine, effectively suppressed CXCL8, and TNF production by THP-1 cells when stimulated with LPS, TNF or IL-1ss. 8-aza-7-deazaadenine 48-85 C-X-C motif chemokine ligand 8 Homo sapiens 110-115 33329929-2 2020 We compared the atherosclerotic burden in non-lower extremity arteries in patients with and without PAD using 18F-sodium fluoride (NaF)-PET/CT. 18f-sodium fluoride 110-129 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 33329933-2 2020 Therefore, we hypothesize that ASCVD risk score is correlated to global cardiac microcalcification, as assessed by 18F-sodium fluoride-positron emission tomography/computed tomography (NaF-PET/CT). 18f-sodium fluoride 115-134 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 33339152-1 2020 The in vitro study objectives were to investigate the effect of arginine (Arg) incorporation in a 5% sodium fluoride (NaF) varnish on its physical and chemical properties including F/Arg release. Arginine 64-72 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 33339152-1 2020 The in vitro study objectives were to investigate the effect of arginine (Arg) incorporation in a 5% sodium fluoride (NaF) varnish on its physical and chemical properties including F/Arg release. Arginine 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 33339152-1 2020 The in vitro study objectives were to investigate the effect of arginine (Arg) incorporation in a 5% sodium fluoride (NaF) varnish on its physical and chemical properties including F/Arg release. Sodium Fluoride 101-116 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 33339152-4 2020 Molecular dynamics were simulated to identify post-dynamics total energy for NaF=Arg/Arg>NaF/ArgNaF/ArgNaF/ArgArg concentration denotes the stabilized environment compared to NaF1 mM, while concentration range 0.25-1 mM were nontoxic and did not lead to oxidative stress, and also did not alter the levels of intracellular melanin or cellular tyrosinase activity, indicating that treatment up to 1 mM NaF is generally safe to melanocytes from both pigmentation phototypes. Melanins 300-307 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 33911791-10 2020 Poly(I:C) increased the expression of psoriasis-related cytokines including tumor necrosis factor-alpha, interleukin-8, and CCL20, and KDM2A inhibitor daminozide enhanced the poly(I:C)-induced cytokine expression. Poly I-C 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 32815062-5 2020 We report that Ad-MSCs treated by DFX resulted in a significantly enhanced mRNA expression of MAPK4 (associated with MAPK signaling pathway), INPP4B (associated with Inositol polyphosphate pathway), VEGF-A and VEGF-C (associated with cytokine-cytokine receptor pathways), IL-8 and its receptor, CXCR2 (associated with IL-8 signaling pathway). Deferoxamine 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 272-276 32815062-5 2020 We report that Ad-MSCs treated by DFX resulted in a significantly enhanced mRNA expression of MAPK4 (associated with MAPK signaling pathway), INPP4B (associated with Inositol polyphosphate pathway), VEGF-A and VEGF-C (associated with cytokine-cytokine receptor pathways), IL-8 and its receptor, CXCR2 (associated with IL-8 signaling pathway). Deferoxamine 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 318-322 33095981-4 2020 Here, we report that ROCK inhibition by Y-27632 reduces levels of IL-1alpha, IL-1beta, IL-6 and IL-8 secreted by senescent normal and dysplastic oral keratinocytes without affecting the permanent cell growth arrest. Y 27632 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 33363521-7 2020 Butyrate administration significantly decreased LPS-induced rise in the clinical score of piglets and colonic histological scores and reduced the susceptibility to LPS-induced severe inflammatory response by decreasing proinflammatory (IL-1beta, IL-6, IL-8, and TNF-alpha) cytokines. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 33113418-9 2020 Here, we summarize the mounting evidence where ASX is shown to exert protective effect by regulating the expression of pro-inflammatory factors IL-1beta, IL-6, IL-8 and TNF-alpha. astaxanthine 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 33357720-5 2020 Additionally, TCDCA decreased tumour necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), IL-6, IL-8 and IL-12 through nuclear factor kappa light chain enhancer of activated B cells (NF-kappaB) activity. Taurochenodeoxycholic Acid 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 33057826-7 2020 RESULTS: In terms of WSL prevention, sodium fluoride (NaF) varnish had the highest cumulative ranking for the short-term decalcification index (99.3%); acidulated phosphate fluoride (APF) foam ranked first for long-term incidence (96.9%), followed by difluorosilane (Dfs) varnish and high-concentration fluoride toothpaste (HFT) (79.4% and 77.4%, respectively). Sodium Fluoride 37-52 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 33057826-7 2020 RESULTS: In terms of WSL prevention, sodium fluoride (NaF) varnish had the highest cumulative ranking for the short-term decalcification index (99.3%); acidulated phosphate fluoride (APF) foam ranked first for long-term incidence (96.9%), followed by difluorosilane (Dfs) varnish and high-concentration fluoride toothpaste (HFT) (79.4% and 77.4%, respectively). Fluorides 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 33075509-11 2020 Following the treatment of epithelial cells with C.jejuni or C.coli, IL-8 and TNF-alpha were significantly increased compared to untreated Caco-2 cells, and the highest IL-8 expression was observed in both C.jejuni and C.coli expressing all CDTs (cdtA, cdtB, and cdtC). 1,5,9-cyclododecatriene 241-245 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 32853623-8 2020 Indeed, structural and sequence analysis evidenced for specificity of molecular interactions with cognate receptor (CXCR1) and glycosaminoglycan (heparin), thus providing evidence for a noticeable functional specificity and divergence between the two IL8 orthologs. Heparin 146-153 C-X-C motif chemokine ligand 8 Homo sapiens 251-254 33045562-5 2020 The results showed that the in vitro treatment of monocytes from preeclamptic women with Sb downregulated the endogenous activation of NF-kappaB and the expression of surface receptors TLR4 and CD64, and reduced the synthesis of the pro-inflammatory cytokines interleukin 1 (IL-1beta), IL-6, IL-8, IL-12p70, IL-23, and tumour necrosis factor alpha (TNF-alpha) compared with cultures not treated with Sb. Silybin 89-91 C-X-C motif chemokine ligand 8 Homo sapiens 292-296 33075509-11 2020 Following the treatment of epithelial cells with C.jejuni or C.coli, IL-8 and TNF-alpha were significantly increased compared to untreated Caco-2 cells, and the highest IL-8 expression was observed in both C.jejuni and C.coli expressing all CDTs (cdtA, cdtB, and cdtC). CDTA 247-251 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 33075509-11 2020 Following the treatment of epithelial cells with C.jejuni or C.coli, IL-8 and TNF-alpha were significantly increased compared to untreated Caco-2 cells, and the highest IL-8 expression was observed in both C.jejuni and C.coli expressing all CDTs (cdtA, cdtB, and cdtC). cdtc 263-267 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 32870388-9 2020 CONCLUSION: Our data suggest an important role of HSC senescence caused by DCA for the malignant biological behaviors of HCC via induction of SASP factors, particularly IL8 and TGFbeta. Deoxycholic Acid 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 32682627-1 2020 OBJECTIVES: The purpose of the current investigation was to evaluate the diagnostic accuracy of amyloid and F-18 sodium fluoride (NaF) positron emission tomography/computed tomography (PET/CT) for the detection of cardiac amyloidosis (CA) using diagnostic accuracy test. f-18 sodium fluoride 108-128 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 32662566-9 2020 beta-TmU had higher IL-8 than their controls while beta-TmN had higher IL-6 and IL-8 than their controls. beta-tmu 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 32662566-9 2020 beta-TmU had higher IL-8 than their controls while beta-TmN had higher IL-6 and IL-8 than their controls. beta-tmn 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 33157159-1 2020 OBJECTIVES: To investigate the remineralising and staining effects of sodium fluoride (NaF) with silver nanoparticles (AgNPs) on artificial dentine caries. Sodium Fluoride 70-85 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 32930782-12 2020 Adequate adherence with aspirin results in an increase in ATL and IL-10 with reduced IL-8 plasma concentration. Aspirin 24-31 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 33157159-1 2020 OBJECTIVES: To investigate the remineralising and staining effects of sodium fluoride (NaF) with silver nanoparticles (AgNPs) on artificial dentine caries. Silver 97-103 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 33281999-8 2020 Beside this, the 18F-NaF detected SM in body segments not routinely scanned in MRI and CT. Samarium 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 33075233-1 2020 Cadmium (Cd) is accumulated in human astrocytes and induces the production of interleukin (IL)-6 and IL-8. Cadmium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 32731110-17 2020 Subsequently, in human osteoblasts treated with sodium fluoride (NaF), the results also showed that NaF caused low expression of miR-4755-5p and increased expression of Cyclin D1. Sodium Fluoride 48-63 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 32731110-17 2020 Subsequently, in human osteoblasts treated with sodium fluoride (NaF), the results also showed that NaF caused low expression of miR-4755-5p and increased expression of Cyclin D1. Sodium Fluoride 48-63 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 33174050-5 2020 ELISA showed that SFN was associated with a time- and dose-dependent reduction in poly(I:C)-stimulated production of interleukin (IL)-8, chemoattractant protein-1, IL-6, MMP-1 and MMP-3 by HCFs. Poly I-C 82-91 C-X-C motif chemokine ligand 8 Homo sapiens 117-135 33075233-1 2020 Cadmium (Cd) is accumulated in human astrocytes and induces the production of interleukin (IL)-6 and IL-8. Cadmium 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 32949185-10 2020 Meta-analysis including the discovery cohort, also showed that binary IL-8 levels >9.3 pg/ml from patients treated with ADT alone was prognostic for poorer OS (HR 1.8, 95% CI: 1.2-2.7, p = .007) and shorter time to CRPC (HR 1.4, 95% CI: 0.99-1.9, p = .057). adt 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 32949185-11 2020 CONCLUSIONS: In the phase 3 CHAARTED study of men with mHSPC at ADT initiation, elevated IL-8 portended worse survival and shorter time to castration-resistant prostate cancer independent of docetaxel administration, metastatic burden, and metachronous versus de novo metastatic presentation. adt 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 33708368-9 2020 Results: Nintedanib addition to HLFs resulted in significant elevations in Gal-3, phospho-signal transducer and activator of transcription 3 (pSTAT3), as well as IL-8 mRNA levels (p < 0.05). nintedanib 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 33006723-3 2020 In conclusion, our study suggests that SARS-CoV-2 antibodies need to be searched in the serum and CSF in patients with GBS living in endemic areas, even in the absence of a clinically severe COVID-19 infection, and that IL-8 pathway can be relevant in Si-GBS pathogenesis. Silicon 252-254 C-X-C motif chemokine ligand 8 Homo sapiens 220-224 32950532-4 2020 VITROCELL cloud chamber exposure of BEAS-2B monolayers increased mitochondrial protein oxidation, expression of the antioxidant enzyme SOD2, activation of NF-kappaB, and secretion of inflammatory cytokines (IL-6 and IL-8). beas 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 33329539-7 2020 This study demonstrates that Z-AAT variant significantly increases the expression of pro-inflammatory cytokines including CXCL-8, CXCL1, LTB4, and TNFalpha in LPS-treated macrophages. z-aat 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 122-128 33208502-6 2020 ACPA-positive B cells in blood and synovial fluid secreted increased amounts of the chemoattractant interleukin-8, which attracted neutrophils, the most abundant immune cell in arthritic joints. arachidonylcyclopropylamide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 32961113-5 2020 This study aims to highlight for the first time the capability of theobromine in protecting the intestinal cell monolayer from a mixture of dietary oxysterols showing an inflammatory action in terms of IL-8 and MCP-1 overproduction. Theobromine 66-77 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 33263062-0 2020 CXCL-8-dependent and -independent neutrophil activation in COPD: experiences from a pilot study of the CXCR2 antagonist danirixin. danirixin 120-129 C-X-C motif chemokine ligand 8 Homo sapiens 0-6 33553467-9 2021 Compared with healthy blood donor controls, CCP donors had significantly higher plasma levels of interferon (IFN)-gamma, interleukin (IL)-10, IL-15, IL-21, and macrophage-inflammatory protein-1, but lower levels of IL-1RA, IL-8, IL-16, and vascular endothelial growth factor-A (P < .0014). ccp 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 33266406-8 2020 At the same time, NaF reacts with active CaCO3 and converts into CaF2. Calcium Carbonate 41-46 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 33244226-7 2020 Moreover, miR-486-5p expression was significantly correlated with the expression of IL-6, IL-8, TNF-alpha, and IFN-gamma. mir-486-5p 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 33223825-6 2020 In addition, we found a positive correlation between CD4+ IL-10+ T lymphocytes and lower limb muscle strength and a negative correlation between CD4+ IL-8+ T lymphocytes and peripheral oxygen saturation and steps per day. Oxygen 185-191 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 33170220-10 2021 Following exposure to deoxynivalenol, the secretion of interleukin (IL)-1beta, IL-6, IL-8, and/or tumor necrosis factor (TNF)-alpha in BEAS-2B cells, as well as EoL-1 cells, increased significantly. deoxynivalenol 22-36 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 33171063-0 2020 Enterobactin induces the chemokine, interleukin-8, from intestinal epithelia by chelating intracellular iron. Iron 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 36-49 33171063-6 2020 Using three human IEC cell-lines with differential basal levels of Lcn2 (i.e. HT29 < DLD-1 < Caco-2/BBe), we demonstrated that iron-free Ent could induce a dose-dependent secretion of the pro-inflammatory chemokine, interleukin 8 (IL-8), in HT29 and DLD-1 IECs, but not in Caco-2/BBe. Iron 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 216-229 33171063-6 2020 Using three human IEC cell-lines with differential basal levels of Lcn2 (i.e. HT29 < DLD-1 < Caco-2/BBe), we demonstrated that iron-free Ent could induce a dose-dependent secretion of the pro-inflammatory chemokine, interleukin 8 (IL-8), in HT29 and DLD-1 IECs, but not in Caco-2/BBe. Iron 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 231-235 33171063-7 2020 Ent-induced IL-8 secretion was dependent on chelation of the labile iron pool and on the levels of intracellular Lcn2. Iron 68-72 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 33171063-8 2020 Accordingly, IL-8 secretion by Ent-treated HT29 cells could be substantially inhibited by either saturating Ent with iron or by adding exogenous Lcn2 to the cells. Iron 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 33171063-11 2020 Intriguingly, formyl peptide receptor (FPR) antagonists (i.e. Boc2, cyclosporine H) abrogated Ent-induced IL-8, implicating that such IEC response could be, in part, dependent on FPR. boc2 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 33171063-11 2020 Intriguingly, formyl peptide receptor (FPR) antagonists (i.e. Boc2, cyclosporine H) abrogated Ent-induced IL-8, implicating that such IEC response could be, in part, dependent on FPR. cyclosporin H 68-82 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 33224901-7 2020 sEVs from TVV-negative but not TVV-positive parasites cultured alone caused NF-kappaB activation and increase of IL-8 and RANTES expression by uterine endocervical cells, which provide innate immune defense at the gate to the upper reproductive tract. tvv 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 32975550-6 2020 Moreover, when PBMC were cultured with degradable Mg, the expression of migration/wound healing related cytokines (interleukin 8, granulocyte-macrophage colony-stimulating factor, monocyte chemoattractant protein 1 and macrophage inflammatory protein 1alpha/beta) was upregulated, accompanied by an increase in the migration ability of HUCPV (cell scratch assay). Magnesium 50-52 C-X-C motif chemokine ligand 8 Homo sapiens 115-178 33174867-5 2020 Our findings indicate that pretreatment with memantine significantly reduced the expression of interleukin (IL)-6 and IL-8, which are both serum markers if AMI severity. Memantine 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 32777211-9 2020 On the other hand, cell area, circularity or aspect ratio were affected by staurosporine in CXCL8 or CXCL10-activated cells, demonstrating a role of PKCalpha in the rearrangement of the cytoskeleton regardless of the effect on the migration. Staurosporine 75-88 C-X-C motif chemokine ligand 8 Homo sapiens 92-97 33251227-16 2020 In multiple linear regression analysis, both peak IL-6 (p = 0.002) and IL-8 (p = 0.01) concentrations remained significantly correlated with GFRiohexol, without collinearity. gfriohexol 141-151 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 33145738-2 2020 This exploratory study sought to assess the potential of hybrid positron-emission tomography (PET)/magnetic resonance imaging (MRI) using 18F-sodium fluoride (18F-NaF) to check simultaneously 18F-NaF uptake, a marker of microcalcifications, and morphological criteria of vulnerability. 18f-sodium fluoride 138-157 C-X-C motif chemokine ligand 8 Homo sapiens 163-166 33145738-9 2020 We found a positive correlation between 18F-NaF uptake and calcium plaque volume and ratio but not with circulating tissue-nonspecific alkaline phosphatase (TNAP) activity and inorganic pyrophosphate (PPi) levels. Calcium 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 33145838-4 2021 We observed inhibition of IL-6 and CXCL8 secretion from both lung fibroblast models by dexamethasone (maximal inhibition 40 - 90%) and the p38 MAPK inhibitor BIRB (maximal inhibition 30 - 60%), used alone and evidence of increased anti-inflammatory effects when used in combination. Dexamethasone 87-100 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 33145838-4 2021 We observed inhibition of IL-6 and CXCL8 secretion from both lung fibroblast models by dexamethasone (maximal inhibition 40 - 90%) and the p38 MAPK inhibitor BIRB (maximal inhibition 30 - 60%), used alone and evidence of increased anti-inflammatory effects when used in combination. birb 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 32889778-10 2020 Icaritin treatment-induced dynamics of serum cytokines IL-6, IL-8, IL-10 and TNF-alpha, and soluble immune checkpoint proteins TIM3, LAG3, CD28, CD80, and CTLA-4 were assessed. icaritin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 32730122-0 2020 Salivary fluoride concentration and retention after rinsing with 0.05 and 0.2% sodium fluoride (NaF) compared with a new high F rinse containing 0.32% NaF. Fluorides 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 33222465-7 2020 Similarly,4-Octyl Itaconate inhibited the secretion of inflammatory cytokines (TNF-alpha, IL-1beta, IL6, and IL-8) by MCs, which was induced by LPS, but SIRT4 knockdown decreases the inhibition of 4-Octyl Itaconate. 4-Octyl Itaconate 10-27 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 33146789-10 2021 In addition, using the ROS inhibitor N-acetyl-L-cysteine (NAC), we observed abrogated mRNA expression of several ARPs and production of inflammatory cytokines/chemokines (IL-6, IL-8, MCP-1, and CCL-5) in the CSE-challenged cells suggesting an important role of ROS in regulating CSE-induced autophagy. ros 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 33146789-10 2021 In addition, using the ROS inhibitor N-acetyl-L-cysteine (NAC), we observed abrogated mRNA expression of several ARPs and production of inflammatory cytokines/chemokines (IL-6, IL-8, MCP-1, and CCL-5) in the CSE-challenged cells suggesting an important role of ROS in regulating CSE-induced autophagy. Acetylcysteine 37-56 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 33146789-10 2021 In addition, using the ROS inhibitor N-acetyl-L-cysteine (NAC), we observed abrogated mRNA expression of several ARPs and production of inflammatory cytokines/chemokines (IL-6, IL-8, MCP-1, and CCL-5) in the CSE-challenged cells suggesting an important role of ROS in regulating CSE-induced autophagy. Acetylcysteine 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 32236723-9 2020 DeltaZ of hydroxypropyl-beta-cyclodextrin:TiF4 72 h was higher than negative control, hydroxypropyl-beta-cyclodextrin, gamma-cyclodextrin, gamma-cyclodextrin:TiF4 1 2 h, gamma-cyclodextrin:TiF4 72 h, and NaF (p < 0.05) and similar to TiF4 and hydroxypropyl-beta-cyclodextrin:TiF4 12 h (p > 0.05). 2-Hydroxypropyl-beta-cyclodextrin 10-41 C-X-C motif chemokine ligand 8 Homo sapiens 204-207 33139632-6 2020 Vadadustat caused a marked decrease in the secretion of IL6 (by 51%), HGF (by 47%), CCL7 (MCP3) (by 42%) and CXCL8 (by 40%). vadadustat 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 109-114 32236723-9 2020 DeltaZ of hydroxypropyl-beta-cyclodextrin:TiF4 72 h was higher than negative control, hydroxypropyl-beta-cyclodextrin, gamma-cyclodextrin, gamma-cyclodextrin:TiF4 1 2 h, gamma-cyclodextrin:TiF4 72 h, and NaF (p < 0.05) and similar to TiF4 and hydroxypropyl-beta-cyclodextrin:TiF4 12 h (p > 0.05). titanium tetrafluoride 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 204-207 32946851-8 2020 Besides, patients with higher fasting plasma glucose (FPG) had higher IL-6, IL-8, CRP, and mortality. Glucose 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 32736336-10 2020 The expression of CXCL8 induced by WNT5A has been significantly reduced by MEK inhibitor, binimetinib. binimetinib 90-101 C-X-C motif chemokine ligand 8 Homo sapiens 18-23 32769069-7 2020 EGCG has been shown to prevent production and mRNA expression of TSLP, interleukin (IL)-1beta, IL-6, and IL-8 by RANKL without cytotoxicity. epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 32629210-0 2020 Upregulation of miR-200c-3p induced by NaF promotes endothelial apoptosis by activating Fas pathway. mir-200c-3p 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 32629210-5 2020 And miR-200c-3p was found to be upregulated in NaF treated HUVECs. mir-200c-3p 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 32815403-9 2020 Paclitaxel exposure reduced IL-8 levels in cancer cell lines, whilst no cytotoxic effect was observed in all cell lines at treatment concentration levels (<= 0.1% (w/v) paclitaxel in silicone). Paclitaxel 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 32246208-1 2020 AIM: To compare the effects of high-dose therapy (HDT consisting of high-dose chemotherapy followed by autologous stem cell transplantation) and conventional-dose chemotherapy (non-HDT) on the uptake of 18F-sodium fluoride (NaF) in the whole bone, pelvis, and femoral neck of multiple myeloma (MM) patients. Sodium Fluoride 207-222 C-X-C motif chemokine ligand 8 Homo sapiens 224-227 32898511-9 2020 LPS, Poly I:C and TNFalpha significantly induce the secretion of IL-6 and IL-8 at all tested time points. Poly I-C 5-13 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 32968431-6 2020 Isoflurane pretreatment decreased HR-induced IL-6 and IL-8 expression levels in A549 cells. Isoflurane 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 31729901-7 2020 Moreover, p38/MAPK inhibitor SB203580 and NF-kappaB inhibitor BAY11-7082 could block the IL-8 up-regulated by X-rays but JNK inhibitor SP600125, ERK inhibitor U0126, ROS Scavenger NAC could not inhibit this phenomenon.Conclusions: X-rays could induce IL-8 production in lung cancer cells, which may be related to the activation of p38/MAPK and NF-kappaB signaling pathway, providing a new point for elucidating the mechanism of radiation pneumonitis. SB 203580 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 33182021-13 2020 Knocking down NEAT1 expression with an ASO suppressed the expression of CXCL8 and TNF-alpha in PMA/ionomycin-stimulated Jurkat cells. Tetradecanoylphorbol Acetate 95-98 C-X-C motif chemokine ligand 8 Homo sapiens 72-77 33182021-13 2020 Knocking down NEAT1 expression with an ASO suppressed the expression of CXCL8 and TNF-alpha in PMA/ionomycin-stimulated Jurkat cells. Ionomycin 99-108 C-X-C motif chemokine ligand 8 Homo sapiens 72-77 31729901-7 2020 Moreover, p38/MAPK inhibitor SB203580 and NF-kappaB inhibitor BAY11-7082 could block the IL-8 up-regulated by X-rays but JNK inhibitor SP600125, ERK inhibitor U0126, ROS Scavenger NAC could not inhibit this phenomenon.Conclusions: X-rays could induce IL-8 production in lung cancer cells, which may be related to the activation of p38/MAPK and NF-kappaB signaling pathway, providing a new point for elucidating the mechanism of radiation pneumonitis. SB 203580 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 31729901-7 2020 Moreover, p38/MAPK inhibitor SB203580 and NF-kappaB inhibitor BAY11-7082 could block the IL-8 up-regulated by X-rays but JNK inhibitor SP600125, ERK inhibitor U0126, ROS Scavenger NAC could not inhibit this phenomenon.Conclusions: X-rays could induce IL-8 production in lung cancer cells, which may be related to the activation of p38/MAPK and NF-kappaB signaling pathway, providing a new point for elucidating the mechanism of radiation pneumonitis. 3-(4-methylphenylsulfonyl)-2-propenenitrile 62-72 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 32660201-8 2020 Conclusion: The obtained results demonstrate that IL-8 and IL-15 could be proposed as potential markers in their optimal cut-off points for distinguishing CD from the NCGS and the healthy control. Cadmium 155-157 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 31729901-7 2020 Moreover, p38/MAPK inhibitor SB203580 and NF-kappaB inhibitor BAY11-7082 could block the IL-8 up-regulated by X-rays but JNK inhibitor SP600125, ERK inhibitor U0126, ROS Scavenger NAC could not inhibit this phenomenon.Conclusions: X-rays could induce IL-8 production in lung cancer cells, which may be related to the activation of p38/MAPK and NF-kappaB signaling pathway, providing a new point for elucidating the mechanism of radiation pneumonitis. 3-(4-methylphenylsulfonyl)-2-propenenitrile 62-72 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 31729901-7 2020 Moreover, p38/MAPK inhibitor SB203580 and NF-kappaB inhibitor BAY11-7082 could block the IL-8 up-regulated by X-rays but JNK inhibitor SP600125, ERK inhibitor U0126, ROS Scavenger NAC could not inhibit this phenomenon.Conclusions: X-rays could induce IL-8 production in lung cancer cells, which may be related to the activation of p38/MAPK and NF-kappaB signaling pathway, providing a new point for elucidating the mechanism of radiation pneumonitis. U 0126 159-164 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 31729901-7 2020 Moreover, p38/MAPK inhibitor SB203580 and NF-kappaB inhibitor BAY11-7082 could block the IL-8 up-regulated by X-rays but JNK inhibitor SP600125, ERK inhibitor U0126, ROS Scavenger NAC could not inhibit this phenomenon.Conclusions: X-rays could induce IL-8 production in lung cancer cells, which may be related to the activation of p38/MAPK and NF-kappaB signaling pathway, providing a new point for elucidating the mechanism of radiation pneumonitis. N-acetylcysteine lysinate 180-183 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 32557721-8 2020 Results indicated that pre-treatment with BaP increased expression of IL-8 in house dust mite-activated EOL-1, BEAS-2B, and A549 cells. Benzo(a)pyrene 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 32614486-9 2020 Similar 18F-NaF tracer uptake patterns were observed between 3 and 12 weeks for the BCP-coated TPU and titanium implants, but not for the uncoated implants. hydroxyapatite-beta tricalcium phosphate 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 32162384-5 2020 Treatment with teneligliptin significantly reduced IL-1beta-induced expression of tumor necrosis factor alpha, IL-6, and IL-8, generation of reactive oxygen species, increase in metalloproteinase 3 (MMP-3) and MMP-13, reduction of tissue inhibitors of matrix metalloproteinase 1 (TIMP-1) and TIMP-2, release of lactate dehydrogenase, and activation of the mitogen-activated protein kinase p38 and nuclear factor kappaB intracellular signaling pathways, among other things. 3-(4-(4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl)pyrrolidin-2-ylcarbonyl)thiazolidine 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 32614486-9 2020 Similar 18F-NaF tracer uptake patterns were observed between 3 and 12 weeks for the BCP-coated TPU and titanium implants, but not for the uncoated implants. Titanium 103-111 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 32830258-8 2020 CDEC exposed to MCM from IgA1-stimulated THP-1 cells (THP-1-IgA-MCM) exhibited markedly increased expression of neutrophil-associated gelatinase (NGAL) and proinflammatory cytokinesinterleukin (IL)-1beta, tumour necrosis factor-alpha, IL-6 and IL-8 compared with MCM from non-IgA-stimulated THP-1 cells (THP-1-MCM). CDEC 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 32979781-11 2020 When conditions of ROS decrease were experienced, an increase in LL37 antimicrobial peptide and a modulation of IL-8 inflammatory response were noted, suggesting improvement in acne signs. Reactive Oxygen Species 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 33130987-9 2020 Autocrine GH-mediated IL-6, IL-8, IL-10 expressions were downregulated by curcumin treatment. Curcumin 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 32898874-7 2020 However, an inhibitory effect of the identified quercetin-3-O-rhamnoside and its aglycone, quercetin, on the release of IL-8 and IL-6 could not be demonstrated. quercitrin 48-72 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 32985128-7 2020 RESULTS: Children exposed to higher IL-1beta, IL-6, IL-8, and IL-10 concentrations had lower BMIz at birth but higher BMIz during childhood. bmiz 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 32985128-7 2020 RESULTS: Children exposed to higher IL-1beta, IL-6, IL-8, and IL-10 concentrations had lower BMIz at birth but higher BMIz during childhood. bmiz 118-122 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 32985128-8 2020 Higher concentrations of IL-8 and IL-1beta were also associated with higher BMIz during infancy (B per log increase in IL-8 = 0.04; 95% CI: 0.02 to 0.07; B per log increase in IL-1beta = 0.03; 95% CI: 0.001 to 0.06). bmiz 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 32985128-8 2020 Higher concentrations of IL-8 and IL-1beta were also associated with higher BMIz during infancy (B per log increase in IL-8 = 0.04; 95% CI: 0.02 to 0.07; B per log increase in IL-1beta = 0.03; 95% CI: 0.001 to 0.06). bmiz 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 32898874-7 2020 However, an inhibitory effect of the identified quercetin-3-O-rhamnoside and its aglycone, quercetin, on the release of IL-8 and IL-6 could not be demonstrated. scutellarein 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 32898874-7 2020 However, an inhibitory effect of the identified quercetin-3-O-rhamnoside and its aglycone, quercetin, on the release of IL-8 and IL-6 could not be demonstrated. Quercetin 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 32920000-6 2020 Chloroquine/hydroxychloroquine + azithromycin interacted with 6 genes (CCL2, CTSB, CXCL8, IL1B, IL6 and TNF), whereas chloroquine and azithromycin affected two additional genes (BCL2L1 and CYP3A4), which might be a reason behind a greater number of consequential diseases. Chloroquine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 33139990-1 2020 Background: The present study aimed to investigate whether dual-phase F-18 sodium-fluoride (NaF) positron emission tomography/computed tomography (PET/CT) could improve the diagnostic accuracy of detecting bone metastasis in cancer patients with a solitary bone lesion compared to conventional F-18 NaF PET/CT. Sodium Fluoride 75-90 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 33139990-1 2020 Background: The present study aimed to investigate whether dual-phase F-18 sodium-fluoride (NaF) positron emission tomography/computed tomography (PET/CT) could improve the diagnostic accuracy of detecting bone metastasis in cancer patients with a solitary bone lesion compared to conventional F-18 NaF PET/CT. Sodium Fluoride 75-90 C-X-C motif chemokine ligand 8 Homo sapiens 299-302 32920000-6 2020 Chloroquine/hydroxychloroquine + azithromycin interacted with 6 genes (CCL2, CTSB, CXCL8, IL1B, IL6 and TNF), whereas chloroquine and azithromycin affected two additional genes (BCL2L1 and CYP3A4), which might be a reason behind a greater number of consequential diseases. Hydroxychloroquine 12-30 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 32918926-5 2020 Interestingly, we found that lebecetin reduced the levels of the pro-inflammatory cytokines TNF-alpha, IL-6, and IL-8 while it partially increased LPS-induced secretion of the immunomodulatory cytokine IL-10. lebecetin 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 32920000-6 2020 Chloroquine/hydroxychloroquine + azithromycin interacted with 6 genes (CCL2, CTSB, CXCL8, IL1B, IL6 and TNF), whereas chloroquine and azithromycin affected two additional genes (BCL2L1 and CYP3A4), which might be a reason behind a greater number of consequential diseases. Azithromycin 33-45 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 32920000-6 2020 Chloroquine/hydroxychloroquine + azithromycin interacted with 6 genes (CCL2, CTSB, CXCL8, IL1B, IL6 and TNF), whereas chloroquine and azithromycin affected two additional genes (BCL2L1 and CYP3A4), which might be a reason behind a greater number of consequential diseases. Chloroquine 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 33114240-9 2020 One of the latter compounds-7,10-diisobutyryloxy-8,9-epoxythymyl isobutyrate-at concentrations 0.5, 1.0 and 2.5 muM, significantly reduced IL-8, IL-1beta and CCL2 excretion by LPS-stimulated human neutrophils. 7,10-diisobutyryloxy-8,9-epoxythymyl isobutyrate 28-76 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 32898567-5 2020 The upregulation of TAZ increased the expression of IL-8 in HCC/CDDP and HCC/Dox cells. Cisplatin 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 33120982-11 2020 18F-NaF wall uptake correlated with CS in the femoral arteries, and aortic wall PWV. Cesium 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 33107041-12 2021 Therefore, the mRNA levels of MCP-1 and IL-8 in hPDLCs were significantly decreased through the vitamin D pathway. Vitamin D 96-105 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 32898567-5 2020 The upregulation of TAZ increased the expression of IL-8 in HCC/CDDP and HCC/Dox cells. Doxorubicin 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 33194843-8 2020 There was some variation between the human isolates, but the water isolate seemed to display the greatest pathogenic potential, demonstrated by the highest levels of virulence gene expression, adhesion to epithelial cells and IL-8 induction. Water 61-66 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 33344897-6 2020 AGN 225660 inhibited RANTES, IL-8, and MCP-1 secretion by at least 50%, from TNFalpha activated human macrophages. agn 225660 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 33114438-13 2020 As a result, we identified that Ac2-26 significantly decreased the expression of TNF-alpha/IFN-gamma-stimulated pro-inflammatory chemokines, including IL-1beta, IL-6, IL-8, MDC, TARC, and TNF-alpha, by inhibiting the activation of MAPK, NF-kappaB, and JAK/STAT pathway in TNF-alpha/IFN-gamma-stimulated HaCaT human keratinocytes. annexin A1 peptide (2-26) 32-38 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 33144864-12 2020 Namely, similar to BM-MSCs, SV-MSCs secreted increased amount of IL-6 and IL-8 after 12- or 24-hour treatment with LPS, PolyI:C, TNFalpha, or IL-1beta, compared to untreated controls. Poly I-C 120-127 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 33192540-4 2020 Imaging with positron emission tomography/computed tomography (PET/CT) using 18F-fluorodeoxyglucose (FDG) and 18F-sodium fluoride (NaF) can non-invasively assess arterial inflammation and microcalcification, respectively. 18f-sodium fluoride 110-129 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 33192540-6 2020 By contrast, NaF uptake reflects the exchange of hydroxyl groups of hydroxyapatite crystals for fluoride producing fluorapatite, a key biochemical step in calcification of atherosclerotic plaque. Durapatite 68-82 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 33192540-6 2020 By contrast, NaF uptake reflects the exchange of hydroxyl groups of hydroxyapatite crystals for fluoride producing fluorapatite, a key biochemical step in calcification of atherosclerotic plaque. Fluorides 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 33192540-6 2020 By contrast, NaF uptake reflects the exchange of hydroxyl groups of hydroxyapatite crystals for fluoride producing fluorapatite, a key biochemical step in calcification of atherosclerotic plaque. fluorapatite 115-127 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 33092250-1 2020 The evidence on atherosclerosis imaging with 18F-sodium-fluoride (NaF) positron emission tomography (PET) is hotly debated because of the different patient characteristics, methodology, vascular beds, etc. 18f-sodium-fluoride 45-64 C-X-C motif chemokine ligand 8 Homo sapiens 66-69 33068297-10 2021 Human VF fibroblasts encapsulated in alginate microspheres induced the production of interleukin (IL)-8 and IL-4 at 24 hours. Alginates 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 85-103 33078100-9 2020 Both TNFalpha and IL-8 in the aqueous humor of PAH group were transiently elevated 1wk post-operation and recovered to normal levels at 1 and 3mo post-operation. p-Aminohippuric Acid 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 33083468-10 2020 Conclusion: Dexmedetomidine can reduce the level of plasma IL-8 and upregulate the expression of AQP1 in the lung tissue of patients undergoing thoracoscopic surgery under one-lung ventilation, but it has no significant effect on the incidence of postoperative PPCs. Dexmedetomidine 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 32829163-6 2020 Similar to the known CXCR2 antagonist SB265610, compound 52 inhibited CXCL8-CXCR2 induced phosphorylation of ERK1/2. 1-(2-bromophenyl)-3-(7-cyano-3H-benzotriazol-4-yl)urea 38-46 C-X-C motif chemokine ligand 8 Homo sapiens 70-75 32829163-7 2020 TUTP compounds also inhibited CXCL8-mediated cell migration and showed synergy with doxorubicin in ovarian cancer cells, thereby supporting TUTPs as promising compounds for cancer treatment. tutp 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 30-35 32829163-7 2020 TUTP compounds also inhibited CXCL8-mediated cell migration and showed synergy with doxorubicin in ovarian cancer cells, thereby supporting TUTPs as promising compounds for cancer treatment. tutps 140-145 C-X-C motif chemokine ligand 8 Homo sapiens 30-35 33066024-12 2020 Quininib significantly downregulated IL-2 and IL-6 in Mel285 cells (p < 0.05) but significantly upregulated IL-10, IL-1beta, IL-2 (p < 0.0001), IL-13, IL-8 (p < 0.001), IL-12p70 and IL-6 (p < 0.05) in OMM2.5 cells. quininib 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 33066647-6 2020 The in vitro results showed that naringenin significantly attenuated CSE-induced up-regulation of IL-8 and TNF-alpha. naringenin 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 32856891-10 2020 Overall, NaF is a better salt than NaCl by having 2.3-fold higher sensitivity, which was confirmed in a DNA sensing assay. Salts 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 32618142-17 2020 Further multivariable analysis showed that phenylalanine >= 112 muM predicted death over 1 year independently of age, APACHE II and SOFA scores, atrial fibrillation, C-reactive protein, cholesterol, pre-albumin, transferrin, and interleukin-8 and interleukin-10. Phenylalanine 43-56 C-X-C motif chemokine ligand 8 Homo sapiens 229-242 32726657-11 2020 NAC significantly decreased malondialdehyde (MDA) (SMD = -1.44 mumol/L; 95% CI: -2.05, -0.84; P < 0.001), IL-8 (WMD = -2.56 pg/ml; 95% CI: -3.89, -1.23; P < 0.001) and homocysteine (WMD = -1.45 pg/ml; 95% CI: -2.74, -0.17; P = 0.027) levels. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 32726657-14 2020 NAC significantly decreased MDA, IL-8, and homocysteine levels. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 32598947-7 2020 The ability of the colchicine analogues with the predicted highest affinity for betaVI-tubulin to dampen neutrophil responses to MSU was determined with in vitro assays that measure MSU-induced production of ROS, release of IL-1 and IL-8, and the increase in the concentration of cytoplasmic calcium. Colchicine 19-29 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 32232846-10 2020 The proportion of leukaemic cells in bone marrow on infusion day and the peaks of IL-6, TNF-alpha and IL-8 levels were correlated with CRS levels. 3-cresol 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 32814232-8 2020 RESULTS: We found that punicalagin and curcumin significantly supressed TNF-induced pro-inflammatory cytokine (IL1A, IL1B, and IL6) and chemokine (CCL2-4, CXCL1, CXCL5 and CXCL8) expression in human placenta, VAT and SAT. Curcumin 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 172-177 32589777-8 2020 The concentration of CBM (12.5%) inhibited the production of IL-6 (p<0.05), IL-8 (p<0.01) and MCP-1 (p<0.005) and augmented the production of IL-10 (p<0.05). N-(4-chlorobenzoyl)melatonin 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 33107903-5 2020 Results: In laser-induced CNV, fursultiamine significantly decreased vascular leakage and lesion size, as well as the numbers of both choroidal and retinal inflammatory cytokines, including IL-1beta, IL-6, IL-8, and TNF-alpha. Fursultiamin 31-44 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 33107903-7 2020 Furthermore, fursultiamine suppressed LPS-induced upregulation of IL-6, IL-8, and monocyte chemoattractant protein-1 in a dose-dependent and time-dependent manner in primary hRPE cells. Fursultiamin 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 33456597-9 2020 Addition of synbiotic to allopurinol leads to a blood uric acid lowering (18.7% vs. 13.3%, p <0.01), CRP reduction (75% vs. 26.3%, p <0.01) as well as decrease of cytokines level: IL-1beta, IL-6, IL-8, IL-10 and TNFalpha (all p <0.001). Allopurinol 25-36 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 32735798-13 2020 All agonists induced the secretion of IL-1ss, IL-8, and TNFalpha in microglia cells while in real-time PCR, LPS and Pam induced the expression of IL-6, IL-1ss and iNOS. pam 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 32578917-9 2020 Aggregation, soft-agar, clonogenic, and scratch assays as well as gene expression analysis collectively confirmed that 4-FPAC minimizes the metastatic property of A549 by downregulating Snail, matrix metalloproteinase 9, and interleukin-8. 4-fpac 119-125 C-X-C motif chemokine ligand 8 Homo sapiens 225-238 33159774-0 2020 Incidental brain metastasis of breast cancer detected on 18F-Sodium Fluoride (NaF) PET-CT. 18F- Sodium Fluoride (NaF) is an excellent bone imaging agent used for skeletal staging but can also be localized in extra osseous calcifying lesions. 18f-sodium fluoride 57-76 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 33159774-0 2020 Incidental brain metastasis of breast cancer detected on 18F-Sodium Fluoride (NaF) PET-CT. 18F- Sodium Fluoride (NaF) is an excellent bone imaging agent used for skeletal staging but can also be localized in extra osseous calcifying lesions. 18f-sodium fluoride 57-76 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 33159774-0 2020 Incidental brain metastasis of breast cancer detected on 18F-Sodium Fluoride (NaF) PET-CT. 18F- Sodium Fluoride (NaF) is an excellent bone imaging agent used for skeletal staging but can also be localized in extra osseous calcifying lesions. 18f- sodium fluoride 91-111 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 33159774-0 2020 Incidental brain metastasis of breast cancer detected on 18F-Sodium Fluoride (NaF) PET-CT. 18F- Sodium Fluoride (NaF) is an excellent bone imaging agent used for skeletal staging but can also be localized in extra osseous calcifying lesions. 18f- sodium fluoride 91-111 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 32794617-4 2020 Uric acid sodium salt induces caspase-1 activation, cell death, and the expression of proinflammatory cytokines, including IL-1alpha, IL-6, and IL-8, in the human keratinocyte HOK-16B cell line. Uric acid sodium salt 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 32768370-1 2020 In recent years, 18F-Sodium Fluoride (NaF)-PET/CT has seen its role in the detection and management of osteoporosis increase. 18f-sodium fluoride 17-36 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 32957145-2 2020 In initial investigations, the dichloromethane extract from the aerial parts of S. orientalis showed distinct inhibitory effects on the release of interleukin-8 in human neutrophils. Methylene Chloride 31-46 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 32957145-7 2020 Three germacranolide sesquiterpene lactones inhibited interleukin-8 production with IC50 values between 1.6 and 6.3 microM, respectively, and tumor necrosis factor-alpha production with IC50 values between 0.9 and 3.3 microM, respectively. germacranolide 6-20 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 32739154-5 2020 For the peroxynitrite-modified proteins, we found a strongly enhanced activation of TLR4 and the pro-inflammatory transcription factor NF-kappaB in stable reporter cell lines as well as increased mRNA expression and secretion of the pro-inflammatory cytokines TNF-alpha, IL-1beta, and IL-8 in human monocytes (THP-1). Peroxynitrous Acid 8-21 C-X-C motif chemokine ligand 8 Homo sapiens 285-289 32957145-7 2020 Three germacranolide sesquiterpene lactones inhibited interleukin-8 production with IC50 values between 1.6 and 6.3 microM, respectively, and tumor necrosis factor-alpha production with IC50 values between 0.9 and 3.3 microM, respectively. sesquiterpene lactones 21-43 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 32730864-8 2020 Abacavir, carbamazepine and clozapine gave positive results with CD86 upregulation and/or IL-8 release, with abacavir also inducing HLA-DR. abacavir 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 32730864-8 2020 Abacavir, carbamazepine and clozapine gave positive results with CD86 upregulation and/or IL-8 release, with abacavir also inducing HLA-DR. Carbamazepine 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 32730864-8 2020 Abacavir, carbamazepine and clozapine gave positive results with CD86 upregulation and/or IL-8 release, with abacavir also inducing HLA-DR. Clozapine 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 32783763-6 2020 CBNPs induced a significant increase in the expressions of IL-8 and IL-6, accompanied by a high level of intracellular HDAC6 mRNA when compared with a blank control group (p < 0.05). cbnps 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 32840447-12 2020 A limited amount of IL-6 and IL-8 was released by ionomycin-exposed HMC-1 cells. Ionomycin 50-59 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 32998161-11 2020 In presence of IL-1beta, TCs showed an upregulation of ADORA2A, SCX and COL3A1 expression and an increase of IL-6, IL-8, PGE2 and VEGF secretion. 9-ethyl-N-(3,4,5-trimethoxyphenyl)carbazole-3-sulfonamide 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 32991579-4 2020 Interaction of the above-mentioned alkaloids with acetylcholinesterase enzyme and interleukins IL-6 and IL-8 was investigated in silico by molecular docking. Alkaloids 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 33093965-8 2020 Results: There was a significant difference between the mean vitamin 25(OH)D (p = 0.001) and IL-8 levels (p = 0.002) before and after vitamin D supplementation. Vitamin D 134-143 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 33003647-11 2020 MiR-342-3p was negatively correlated with TIMP-1, IL-6, IL-8, TNF-alpha, HbA1c and CXCR2, whilst miR-342-5p was negatively correlated with TIMP-1, IL-6, IL-8 and HbA1c. mir-342-3p 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 33093965-0 2020 Modulation of Interleukin-8 Production by Vitamin D Supplementation in Indonesian Patients with Diabetic Polyneuropathy: A Randomized Clinical Trial. Vitamin D 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 33093965-1 2020 Objectives: We sought to assess the modulation of interleukin-8 (IL-8) production by vitamin D supplementation in Indonesian patients with diabetic polyneuropathy (DPN). Vitamin D 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 33093965-1 2020 Objectives: We sought to assess the modulation of interleukin-8 (IL-8) production by vitamin D supplementation in Indonesian patients with diabetic polyneuropathy (DPN). Vitamin D 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 32991579-11 2020 Stepharine inhibited considerably the production of IL-8 in comparison to 5-N-methylmaytenine, which showed a dose dependent action (inhibitory at the IC50 dose, and stimulatory at the twofold IC50 one). stepharine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 32993127-5 2020 LPS alone or together with cyclic dinucleotides elevated IL-8 levels. cyclic dinucleotides 27-47 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 32975624-14 2021 Additionally, SSNB and ANB with DEX tended to result in a later mean timing of rebound pain accompanied by significant changes in IL-8, IL-1beta, and serotonin levels within 48 h after the operation. ssnb 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 33101052-10 2020 We also found that ouabain (100 nM) promoted the secretion of IL-6, IL-8, GM-CSF, and TNF-alpha from the skeletal muscle cells of healthy subjects, and the secretion of GM-CSF from cells of subjects with the type 2 diabetes. Ouabain 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 32975624-14 2021 Additionally, SSNB and ANB with DEX tended to result in a later mean timing of rebound pain accompanied by significant changes in IL-8, IL-1beta, and serotonin levels within 48 h after the operation. alpha-naphthyl butyrate 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 32975624-14 2021 Additionally, SSNB and ANB with DEX tended to result in a later mean timing of rebound pain accompanied by significant changes in IL-8, IL-1beta, and serotonin levels within 48 h after the operation. Dexmedetomidine 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 32973190-10 2020 In human corneal epithelial cells, secretion of IL-6 and IL-8 in both apical and basolateral media was promoted significantly by perfluorooctanoic acid treatment. perfluorooctanoic acid 129-151 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 32610185-5 2020 Additionally, TJ and siMyD88 significantly attenuated cell migration and invasion, inhibited EMT-like progression and reduced cytokine (IL-6, IL-8, TGF-beta1 and TNF-alpha) secretion induced by LPS. simyd88 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 32794529-8 2020 Moreover, as compared to the control group, sows and newborn piglets in the Na2SeO3 and HMSeBA groups had a lower serum interleukin-6 (p < 0.05) concentration, and placentas in the HMSeBA group had lower IL-1beta, IL-6 and IL-8 gene expression (p < 0.05). na2seo3 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 33230450-7 2020 Mechanically, miR-146b-5p suppressed nuclear factor kappaB (NF-kappaB) activity and NF-kappaB-related IL-6 and IL-8 production by targeting IRAK1. mir-146b-5p 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 32977686-9 2020 Finally, the inflammatory response in the HGF-1 cells after their exposure to GSH-AgNPs was measured as the production of immune markers (interleukins 6 and 8 (IL-6 and IL-8) and tumor necrosis factor-alpha (TNF-alpha)). gsh-agnps 78-87 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 32961947-6 2020 The hexane fraction exerted the most potent anti-inflammatory effect, suppressing C. acnes-induced interleukin-8 (IL-8) production by 36%. Hexanes 4-10 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 32961947-7 2020 The ethanol-soluble fraction (ESF), which was separated from the n-hexane fraction, significantly inhibited C. acnes-induced activation of mitogen-activated protein kinase (MAPK)-mediated cellular IL-8 production. Ethanol 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 32961947-7 2020 The ethanol-soluble fraction (ESF), which was separated from the n-hexane fraction, significantly inhibited C. acnes-induced activation of mitogen-activated protein kinase (MAPK)-mediated cellular IL-8 production. n-hexane 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 32961947-10 2020 Using co-cultures of C. acnes and THP-1 cells, beta-ionone, a compound of the ESF, reduced the production of IL-1beta and IL-8 up to 40% and 18%, respectively. beta-ionone 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 32915344-13 2020 The BPL can reduce PET acquisition to 90 s/bed in 18F-NaF PET/CT imaging. Fluorine-18 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 32973970-1 2020 Pyrazolyl-urea and dihydro-imidazo-pyrazolyl-urea compounds (STIRUR 13, STIRUR 41 and BUR 12) have been demonstrated to exert a strong inhibitory effect on interleukin 8 or N-formyl-methionyl-leucyl-phenylalanine-induced chemotaxis of human neutrophils. Urea 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 156-169 32973970-1 2020 Pyrazolyl-urea and dihydro-imidazo-pyrazolyl-urea compounds (STIRUR 13, STIRUR 41 and BUR 12) have been demonstrated to exert a strong inhibitory effect on interleukin 8 or N-formyl-methionyl-leucyl-phenylalanine-induced chemotaxis of human neutrophils. Urea 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 156-169 32867889-9 2020 Gender-differentiated correlations of VFA with clinical and inflammatory variables were observed in age, FeNO, immunoglobulin E, blood total white cells and neutrophils, and sputum IL-1beta and IL-8. Fatty Acids, Volatile 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 32886659-7 2020 In CS relative to OS, there were numerous differentially expressed genes including pro-inflammatory cytokines (IL17A, IL8, IL19, IL20 and OSM) and chemokines involved in immune cell activation and recruitment (CCL20, CCL27 and CXCL6). Cesium 3-5 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 32927792-7 2020 Both formulations, however, delivered sufficient amounts of DXM to effectively suppress the production of interleukin-6 (IL-6), interleukin-8 (IL-8) and Thymic Stromal Lymphopoietin (TSLP). Dexamethasone 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 32927792-7 2020 Both formulations, however, delivered sufficient amounts of DXM to effectively suppress the production of interleukin-6 (IL-6), interleukin-8 (IL-8) and Thymic Stromal Lymphopoietin (TSLP). Dexamethasone 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 32669746-4 2020 In this model, indole modulates transcription factor nuclear factor kappa B (NF-kappaB) and produces the chemokine interleukin-8 (IL-8) through the activation of the aryl hydrocarbon receptor (AhR). indole 15-21 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 32825908-0 2020 Metabolomic profiling of parapneumonic effusion reveals a regulatory role of dipeptides in interleukin-8 production in neutrophil-like cells. Dipeptides 77-87 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 32825908-6 2020 Furthermore, with integrated proteomic and transcriptomic analyses of PPEs, the levels of dipeptides were strongly associated with the production of interleukin-8 (IL-8), an inflammation-associated cytokine. Dipeptides 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 32825908-6 2020 Furthermore, with integrated proteomic and transcriptomic analyses of PPEs, the levels of dipeptides were strongly associated with the production of interleukin-8 (IL-8), an inflammation-associated cytokine. Dipeptides 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 32825908-7 2020 The production of IL-8 indeed increased upon the treatment of HL-60-derived neutrophilic cells with dipeptides, Gly-Val and Gly-Tyr. Dipeptides 100-110 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 32825908-7 2020 The production of IL-8 indeed increased upon the treatment of HL-60-derived neutrophilic cells with dipeptides, Gly-Val and Gly-Tyr. glycylvaline 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 32825908-7 2020 The production of IL-8 indeed increased upon the treatment of HL-60-derived neutrophilic cells with dipeptides, Gly-Val and Gly-Tyr. glycyltyrosine 124-131 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 32448093-4 2020 The active mixture also reduced the production of PGE2 and IL-8 in PMA-induced A549 cells. Tetradecanoylphorbol Acetate 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 32564453-8 2020 RESULTS: Compared to PF and PQ groups, mRNA and protein expression of IL-6, IL-8, and IL-1beta increased in samples from the BAK group in a time-dependent fashion, whereas all other cytokines showed a non-significant increase. Benzalkonium Compounds 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 31804143-1 2020 Positron emission tomography (PET) with 18F-Sodium fluoride (18F-NaF) has emerged as a promising non-invasive imaging modality to identify high-risk and ruptured atherosclerotic plaques. Sodium Fluoride 40-59 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 31804143-1 2020 Positron emission tomography (PET) with 18F-Sodium fluoride (18F-NaF) has emerged as a promising non-invasive imaging modality to identify high-risk and ruptured atherosclerotic plaques. CP-18 compound 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 31804143-2 2020 By visualizing microcalcification, 18F-NaF PET holds clinical promise in refining how we evaluate coronary artery disease, shifting our focus from assessing disease burden to atherosclerosis activity. CP-18 compound 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 31804143-3 2020 In this review we provide an overview of studies that have utilized 18F-NaF PET for imaging atherosclerosis. CP-18 compound 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 31804143-4 2020 We discuss the associations between traditional coronary artery disease measures (risk factors) and 18F-NaF plaque activity. CP-18 compound 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 31804143-5 2020 We also present the data on the histological validation as well as show how 18F-NaF uptake is associated with plaque morphology on intravascular and computed tomography imaging. CP-18 compound 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 31804143-6 2020 Finally, we discuss the technical challenges associated with 18F-NaF coronary PET highlighting recent advances in this area. CP-18 compound 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 32383139-5 2020 Moreover, CXCL8, CXCL10, CXCL11, PLSCR1, RIPK2 and USP18 were found to be potentially associated with chemo-resistance related to CAFs and prognosis of BC. cafs 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 10-15 32532788-0 2020 Plasma Interleukin-8 is a biomarker for TAK1 activation and predicts resistance to nanoliposomal irinotecan in patients with gemcitabine-refractory pancreatic cancer. Irinotecan 97-107 C-X-C motif chemokine ligand 8 Homo sapiens 7-20 32532788-0 2020 Plasma Interleukin-8 is a biomarker for TAK1 activation and predicts resistance to nanoliposomal irinotecan in patients with gemcitabine-refractory pancreatic cancer. gemcitabine 125-136 C-X-C motif chemokine ligand 8 Homo sapiens 7-20 32554157-15 2020 Methylprednisolone administration in six patients had no significant influence on the studied surface receptors but led to lower IL-8 and higher IL-10 plasma concentrations. Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 32532788-12 2020 Conclusion Our study identified interleukin-8 as the most significant circulating factor for TAK1 pathway activation and candidates interleukin-8 as a potential predictive biomarker of resistance to nal-IRI in gemcitabine-refractory pancreatic cancer patients. gemcitabine 210-221 C-X-C motif chemokine ligand 8 Homo sapiens 132-145 32921364-5 2020 Administration of fish oil resulted in lower total blood leukocyte number (P = 0.04), CRP (P = 0.013), interleukin-8 (P = 0.05) and intercellular adhesion molecule 1 (P = 0.01) concentrations, multiple organ dysfunction score, sequential organ failure assessment score (P = 0.004), early warning score (P = 0.01), and systemic inflammatory response syndrome (P = 0.03) compared to the control group. Fish Oils 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 103-116 32293791-7 2020 In addition, NaF exposure increased the protein expression of p-ERK1/2 and decreased the protein expressions of Nrf2 and HO-1, as well as facilitated increasing ROS, 4-hydroxynonenal (4-HNE), and 8-Hydroxy-2"-deoxyguanosine (8-OHdG). 8-ohdg 196-223 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 32293791-5 2020 Moreover, pretreatment with emodin was used to shed light on the neuroprotective effects in NaF-induced toxicity in SH-SY5Y cells. Emodin 28-34 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 32293791-7 2020 In addition, NaF exposure increased the protein expression of p-ERK1/2 and decreased the protein expressions of Nrf2 and HO-1, as well as facilitated increasing ROS, 4-hydroxynonenal (4-HNE), and 8-Hydroxy-2"-deoxyguanosine (8-OHdG). ros 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 32293791-7 2020 In addition, NaF exposure increased the protein expression of p-ERK1/2 and decreased the protein expressions of Nrf2 and HO-1, as well as facilitated increasing ROS, 4-hydroxynonenal (4-HNE), and 8-Hydroxy-2"-deoxyguanosine (8-OHdG). 8-ohdg 225-231 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 32293791-7 2020 In addition, NaF exposure increased the protein expression of p-ERK1/2 and decreased the protein expressions of Nrf2 and HO-1, as well as facilitated increasing ROS, 4-hydroxynonenal (4-HNE), and 8-Hydroxy-2"-deoxyguanosine (8-OHdG). 4-hydroxy-2-nonenal 166-182 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 32293791-7 2020 In addition, NaF exposure increased the protein expression of p-ERK1/2 and decreased the protein expressions of Nrf2 and HO-1, as well as facilitated increasing ROS, 4-hydroxynonenal (4-HNE), and 8-Hydroxy-2"-deoxyguanosine (8-OHdG). 4-hydroxy-2-nonenal 184-189 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 32293791-8 2020 Pretreatment with emodin significantly recovered these alterations caused by NaF. Emodin 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 32515014-13 2020 The expression of IL-8 gene was high for all materials, ProRoot MTA caused significant overexpression, and the addition of RSV reduced the expression of IL-8 in the Calcimol LC, TheraCal LC and ProRoot MTA groups and led to increased expression of IL-10 in the Calcimol LC, Life and Biodentine groups. Resveratrol 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 32964957-12 2020 Moreover, relative levels of IL-6, IL-8, TNF-alpha, and MMP3/9/13 were significantly suppressed by SF1670 stimuli compared with IL-1beta group. SF1670 99-105 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 32717131-0 2020 Interleukin-8 drives CD38 to form NAADP from NADP+ and NAAD in the endolysosomes to mobilize Ca2+ and effect cell migration. NAADP 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 32717131-0 2020 Interleukin-8 drives CD38 to form NAADP from NADP+ and NAAD in the endolysosomes to mobilize Ca2+ and effect cell migration. NADP 45-50 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. NAADP 47-52 C-X-C motif chemokine ligand 8 Homo sapiens 234-247 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. NAADP 47-52 C-X-C motif chemokine ligand 8 Homo sapiens 249-252 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. Niacinamide 71-83 C-X-C motif chemokine ligand 8 Homo sapiens 234-247 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. Niacinamide 71-83 C-X-C motif chemokine ligand 8 Homo sapiens 249-252 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. NADP 94-137 C-X-C motif chemokine ligand 8 Homo sapiens 234-247 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. NADP 94-137 C-X-C motif chemokine ligand 8 Homo sapiens 249-252 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. NADP 139-144 C-X-C motif chemokine ligand 8 Homo sapiens 234-247 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. NADP 139-144 C-X-C motif chemokine ligand 8 Homo sapiens 249-252 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. nicotinic acid adenine dinucleotide 167-202 C-X-C motif chemokine ligand 8 Homo sapiens 234-247 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. nicotinic acid adenine dinucleotide 167-202 C-X-C motif chemokine ligand 8 Homo sapiens 249-252 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. nicotinic acid adenine dinucleotide 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 234-247 32717131-3 2020 We discovered that CD38 catalyzes synthesis of NAADP by exchanging the nicotinamide moiety of nicotinamide adenine dinucleotide phosphate (NADP+ ) for the NA group of nicotinic acid adenine dinucleotide (NAAD) inside endolysosomes of interleukin 8 (IL8)-treated lymphokine-activated killer (LAK) cells. nicotinic acid adenine dinucleotide 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 249-252 32717131-4 2020 Upon IL8 stimulation, cytosolic NADP+ is transported to acidified endolysosomes via connexin 43 (Cx43) and gated by cAMP-EPAC-RAP1-PP2A signaling. NADP 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 32717131-4 2020 Upon IL8 stimulation, cytosolic NADP+ is transported to acidified endolysosomes via connexin 43 (Cx43) and gated by cAMP-EPAC-RAP1-PP2A signaling. Cyclic AMP 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 32962811-4 2020 The expression of four key genes involved in inflammation and apoptosis including IL-8, IL-1beta, IL-10 and Bcl2 depicted that the MTX-SA had controversial behavior in different doses on the inflammatory transcription. mtx-sa 131-137 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 32645629-7 2020 We found that DMF significantly improved cell viability and reduced the expression of pro-inflammatory cytokines and chemokines, including IL-6, IL-8, and MCP-1. Dimethyl Fumarate 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 32515014-13 2020 The expression of IL-8 gene was high for all materials, ProRoot MTA caused significant overexpression, and the addition of RSV reduced the expression of IL-8 in the Calcimol LC, TheraCal LC and ProRoot MTA groups and led to increased expression of IL-10 in the Calcimol LC, Life and Biodentine groups. Resveratrol 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 32726647-4 2020 OxLDL priming induced a proinflammatory memory with increased production of inflammatory cytokines such as IL-6, IL-8 and MCP-1 in response to PAM3cys4 restimulation. pam3cys4 143-151 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 32729244-3 2020 In this randomized, placebo-controlled trial, we aimed to evaluate the potential reflection of short-term xylitol consumption on pro-inflammatory cytokines (TNF-alpha, IL-6 and IL-8) and S. mutans counts by ELISA and qPCR (Quantitative real-time PCR), respectively. Xylitol 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 33181840-11 2020 CONCLUSION(S): The CFDs containing NaF only have higher concentrations of bioavailable fluoride. Fluorides 87-95 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 32945158-9 2020 Histamine is involved in the expression of chemokine IL-8 and cytokine IL-6, an effect that can be inhibited by histamine receptor antagonists. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 32945158-9 2020 Histamine is involved in the expression of chemokine IL-8 and cytokine IL-6, an effect that can be inhibited by histamine receptor antagonists. Histamine 112-121 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 32387042-7 2020 However, in CF macrophages lenabasum downregulated macrophage polarization into the pro-inflammatory M1 phenotype and secretion of the pro-inflammatory cytokines IL-8 and TNF-alpha in a dose-dependent manner. lenabasum 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 32015430-6 2020 Mono-n-butyl phthalate (MBP) was correlated with higher IL-1beta, IL-6, and CRP expression in placentae of male fetuses and with higher IL-6, CRP, MCP-1, IL-8, IL-10, and CD68 expression in placentae of female fetuses. monobutyl phthalate 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 32015430-6 2020 Mono-n-butyl phthalate (MBP) was correlated with higher IL-1beta, IL-6, and CRP expression in placentae of male fetuses and with higher IL-6, CRP, MCP-1, IL-8, IL-10, and CD68 expression in placentae of female fetuses. monobutyl phthalate 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 32780615-2 2020 CXCL8 harbors 2 disulfide bonds for its stability. Disulfides 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 32534879-1 2020 In this work, a multifunctional hierarchical nanoformulation composed of biodegradable chitosan (CS) coated poly (lactic-co-glycolic acid) (PLGA) nanocarriers loaded with docetaxel (Doc) and interleukin-8 (IL-8) small interfering RNA (siRNA) electrostatically bound to upconversion nanoparticles (UCNPs), is developed to treat castration-resistant prostate cancer (CRPC). Chitosan 97-99 C-X-C motif chemokine ligand 8 Homo sapiens 191-204 32534879-1 2020 In this work, a multifunctional hierarchical nanoformulation composed of biodegradable chitosan (CS) coated poly (lactic-co-glycolic acid) (PLGA) nanocarriers loaded with docetaxel (Doc) and interleukin-8 (IL-8) small interfering RNA (siRNA) electrostatically bound to upconversion nanoparticles (UCNPs), is developed to treat castration-resistant prostate cancer (CRPC). Chitosan 97-99 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 31907823-8 2020 RESULTS: The results showed that AS-IV significantly reduced the levels of ROS, LDH, MDA, IL-8, IL-1beta, and IL-6, and increased the level of SOD in intermittent hypoxia-induced Beas-2B cells. astragaloside A 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 32249518-8 2020 Carvacrol had a positive effect on the reduction of interleukin (IL)-1beta, IL-4, IL-8 and malondialdehyde (MDA); however, the analysis indicated that carvacrol had no effect on IL-6 and tumor necrosis factor alpha (TNF-alpha), probably due to the methodological quality of the studies and their heterogeneity. carvacrol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 32542667-7 2020 The effect of a combination with two natural compounds, oleanolic acid (OA) and ursolic acid (UA), was evaluated on the expression of the IL-8 axis and epithelial cell growth. Oleanolic Acid 56-70 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 32542667-7 2020 The effect of a combination with two natural compounds, oleanolic acid (OA) and ursolic acid (UA), was evaluated on the expression of the IL-8 axis and epithelial cell growth. Oleanolic Acid 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 32542667-7 2020 The effect of a combination with two natural compounds, oleanolic acid (OA) and ursolic acid (UA), was evaluated on the expression of the IL-8 axis and epithelial cell growth. ursolic acid 80-92 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 32542667-7 2020 The effect of a combination with two natural compounds, oleanolic acid (OA) and ursolic acid (UA), was evaluated on the expression of the IL-8 axis and epithelial cell growth. ursolic acid 94-96 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 32198119-4 2020 PURPOSE: To examine fluorine-18 sodium fluoride (18F-NaF) PET/computed tomography (PET/CT) findings in patients with inflammatory low back pain and evaluate the utility of this modality in the diagnosis of ankylosing spondylitis (AS) according to the Assessment of SpondyloArthritis International Society (ASAS) criteria. fluorine-18 sodium fluoride 20-47 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 32198119-14 2020 CONCLUSION: 18F-NaF PET/CT yielded significantly different findings between the two groups according to the ASAS criteria and is useful for diagnosing AS. asas 108-112 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 33629550-8 2020 Conclusion: 100 mug/ml Nano-SiO2 combined with 31C cold exposure can synergistically reduce the activity of A549 cells and increase the expression level of inflammatory factors IL-6 and IL-8 . Silicon Dioxide 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 32859169-6 2020 RESULTS: In non-DS patients, IL-8 plasma levels were significantly reduced in the seventh day of ATRA treatment (34.16; 6.99 to 147.11 pg mL- 1 in D0 vs. 10.9; 0 to 26.81 pg mL- 1 in D7; p = 0.02) whereas their levels did not discriminate between DS and non-DS development during the entire induction period (all p > 0.05 in D0, D3, and D7). Tretinoin 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 32929393-2 2020 18F-sodium fluoride (18F-NaF) is a sensitive PET radiotracer for detection of abnormal bone metabolism and, therefore, is particularly suited to assess the degree of bone involvement in MM patients. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 32786371-1 2021 Calcium minerals such as hydroxyapatite (HAp) can be detected non-invasively in vivo using nuclear imaging agents such as [18F]NaF (available from cyclotrons), for positron emission tomography (PET) and 99mTc-radiolabelled bisphosphonates (BP; available from 99mTc generators for single photon emission computed tomography (SPECT) or scintigraphy). Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 32786371-1 2021 Calcium minerals such as hydroxyapatite (HAp) can be detected non-invasively in vivo using nuclear imaging agents such as [18F]NaF (available from cyclotrons), for positron emission tomography (PET) and 99mTc-radiolabelled bisphosphonates (BP; available from 99mTc generators for single photon emission computed tomography (SPECT) or scintigraphy). Durapatite 25-39 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 32786865-5 2020 Cytokines IL-8 and IL-6, production was significantly reduced by 40% and 51%, respectively with 1 mM pre-treatment of gamma-EV. gamma-ev 118-126 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 32641497-3 2020 Herein, we demonstrate that 2-12(S)-HETE-lysophospholipids as well as non-esterified 12(S)-HETE are potent lipid mediators that activate THP-1 human monocytic cells to generate tumor necrosis factor alpha (TNFalpha) and interleukin 8 (IL8). 2-12(s)-hete-lysophospholipids 28-58 C-X-C motif chemokine ligand 8 Homo sapiens 220-233 32974315-13 2020 In all scenarios, among the tested mediators the most pronounced anti-inflammatory effect of MP was observed for IL-8. Methylprednisolone 93-95 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 32641497-3 2020 Herein, we demonstrate that 2-12(S)-HETE-lysophospholipids as well as non-esterified 12(S)-HETE are potent lipid mediators that activate THP-1 human monocytic cells to generate tumor necrosis factor alpha (TNFalpha) and interleukin 8 (IL8). 2-12(s)-hete-lysophospholipids 28-58 C-X-C motif chemokine ligand 8 Homo sapiens 235-238 32641497-3 2020 Herein, we demonstrate that 2-12(S)-HETE-lysophospholipids as well as non-esterified 12(S)-HETE are potent lipid mediators that activate THP-1 human monocytic cells to generate tumor necrosis factor alpha (TNFalpha) and interleukin 8 (IL8). 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 220-233 32641497-3 2020 Herein, we demonstrate that 2-12(S)-HETE-lysophospholipids as well as non-esterified 12(S)-HETE are potent lipid mediators that activate THP-1 human monocytic cells to generate tumor necrosis factor alpha (TNFalpha) and interleukin 8 (IL8). 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 235-238 32923106-11 2020 CONCLUSION: There was a positive correlation between TG/HDL ratio with global cardiac microcalcification assessed by NaF-PET/CT imaging. Triglycerides 53-55 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 32814567-8 2020 Chitin surface was used to develop a sandwich ELISA to detect the chimeric human protein c-myc-GST-IL8 cloned and expressed in Escherichia coli. Chitin 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 32827640-14 2020 The capacity of PM10 to promote pro-inflammatory cytokines such as IL-8 and IL-23, likely to promote a Th2 profile, suggests these effects might be linked to worsening of chronic respiratory disease as these mediators are linked to asthma. pm10 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 32827640-14 2020 The capacity of PM10 to promote pro-inflammatory cytokines such as IL-8 and IL-23, likely to promote a Th2 profile, suggests these effects might be linked to worsening of chronic respiratory disease as these mediators are linked to asthma. th2 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 32512068-4 2020 TAMs in IBC secrete high levels of the cytokines interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1/CCL2) compared to non-IBC patients. tams 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 32913546-0 2020 Nintedanib ameliorates tracheal stenosis by activating HDAC2 and suppressing IL-8 and VEGF in rabbit. nintedanib 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 32913546-10 2020 The mRNA of HDAC2 was increased and that of IL-8 and VEGF was decreased significantly in the tracheal tissue following nintedanib treatment. nintedanib 119-129 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 32913546-12 2020 Budesonide treatment also resulted in increased HDAC2 expression and decreased IL-8 and VEGF expression. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 32913546-15 2020 Therefore, it is concluded that nintedanib alleviates the acquired tracheal stenosis by activating HDAC2 expression and suppressing IL-8 and VEGF expression, and may offer new option to medical treatment for the disease. nintedanib 32-42 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 32512068-4 2020 TAMs in IBC secrete high levels of the cytokines interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1/CCL2) compared to non-IBC patients. tams 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 32512068-8 2020 Dasatinib, an inhibitor of p-Src, and U0126, an inhibitor of p-Erk1/2, down-regulated invasion and expression of CTSB by HCC70 and SUM149 cells, a mechanism that is reversed by IL-8 and MCP-1/CCL2. Dasatinib 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 32512068-8 2020 Dasatinib, an inhibitor of p-Src, and U0126, an inhibitor of p-Erk1/2, down-regulated invasion and expression of CTSB by HCC70 and SUM149 cells, a mechanism that is reversed by IL-8 and MCP-1/CCL2. U 0126 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 32691597-0 2020 Synthesis of Acyl Fluorides from Carboxylic Acids Using NaF-Assisted Deoxofluorination with XtalFluor-E. deoxofluorination 69-86 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 32633119-0 2020 NaF/RbF treated Cu(In,Ga)Se2 thin-film solar cell absorbers: Distinct surface modifications caused by two different types of Rubidium chemistry. Copper 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 32691597-0 2020 Synthesis of Acyl Fluorides from Carboxylic Acids Using NaF-Assisted Deoxofluorination with XtalFluor-E. diethylaminodifluorosulfinium tetrafluoroborate 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 32691597-2 2020 This transformation, assisted by a catalytic amount of NaF, occurs at room temperature in EtOAc, where XtalFluor-E behaves as the activating agent and the fluoride source. diethylaminodifluorosulfinium tetrafluoroborate 103-114 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 32691597-2 2020 This transformation, assisted by a catalytic amount of NaF, occurs at room temperature in EtOAc, where XtalFluor-E behaves as the activating agent and the fluoride source. Fluorides 155-163 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 32691597-0 2020 Synthesis of Acyl Fluorides from Carboxylic Acids Using NaF-Assisted Deoxofluorination with XtalFluor-E. acyl fluorides 13-27 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 32691597-0 2020 Synthesis of Acyl Fluorides from Carboxylic Acids Using NaF-Assisted Deoxofluorination with XtalFluor-E. Carboxylic Acids 33-49 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 32633119-0 2020 NaF/RbF treated Cu(In,Ga)Se2 thin-film solar cell absorbers: Distinct surface modifications caused by two different types of Rubidium chemistry. Rubidium 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 32633119-3 2020 The already Cu deficient surface region after NaF PDT, which is modeled as a Cu:(In+Ga):Se = 1:5:8 phase, shows further depletion after NaF/RbF PDT and seems to incorporate some Rb. Copper 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 32633119-3 2020 The already Cu deficient surface region after NaF PDT, which is modeled as a Cu:(In+Ga):Se = 1:5:8 phase, shows further depletion after NaF/RbF PDT and seems to incorporate some Rb. Copper 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 32633119-3 2020 The already Cu deficient surface region after NaF PDT, which is modeled as a Cu:(In+Ga):Se = 1:5:8 phase, shows further depletion after NaF/RbF PDT and seems to incorporate some Rb. Copper 77-79 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 32633119-3 2020 The already Cu deficient surface region after NaF PDT, which is modeled as a Cu:(In+Ga):Se = 1:5:8 phase, shows further depletion after NaF/RbF PDT and seems to incorporate some Rb. Rubidium 140-142 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 32633119-4 2020 Additionally, we have found strong indications for the NaF/RbF PDT induced formation of a Rb-In-Se-type compound with a 1:1:2 stoichiometry partially covering the absorber surface. rb-in 90-95 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 32543782-8 2020 RESULTS: The release of IL-8 was significantly increased after exposure to TEGDMA, Bis-GMA, UDMA, or TEGDMA in combination with Bis-GMA or UDMA compared to the unstimulated controls. triethylene glycol dimethacrylate 75-81 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 32691592-1 2020 NaMoO3F and Na5W3O9F5 were synthesized by solvothermal reaction of MoO3 and WO3, respectively, with NaF in nonaqueous solvents. namoo3f 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 32691592-1 2020 NaMoO3F and Na5W3O9F5 were synthesized by solvothermal reaction of MoO3 and WO3, respectively, with NaF in nonaqueous solvents. na5w3o9f5 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 32691592-1 2020 NaMoO3F and Na5W3O9F5 were synthesized by solvothermal reaction of MoO3 and WO3, respectively, with NaF in nonaqueous solvents. molybdenum trioxide 2-6 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 32691592-1 2020 NaMoO3F and Na5W3O9F5 were synthesized by solvothermal reaction of MoO3 and WO3, respectively, with NaF in nonaqueous solvents. wo3 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 32691592-4 2020 In the case of the reaction of MoO3 with NaF, the kind of solvent largely affected the obtained morphologies of NaMoO3F. molybdenum trioxide 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 32691592-4 2020 In the case of the reaction of MoO3 with NaF, the kind of solvent largely affected the obtained morphologies of NaMoO3F. namoo3f 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 32691592-6 2020 In addition, the solvothermal reaction of WO3 with NaF led to the formation of Na5W3O9F5. wo3 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 32691592-6 2020 In addition, the solvothermal reaction of WO3 with NaF led to the formation of Na5W3O9F5. na5w3o9f5 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 32691592-8 2020 The effect of the solvents on the morphologies of the obtained oxyfluorides probably resulted from the difference of the solubility of NaF and the subsequent dissolution ratio of MoO3 or WO3 in the used solvents. fluorine monoxide 63-75 C-X-C motif chemokine ligand 8 Homo sapiens 135-138 32785678-8 2020 Results: Trehalose reduced the proinflammatory mediators TNF-alpha, IL-1beta, IL-6, and IL-8 in primary HCECs at 450 mOsM. Trehalose 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 32335896-5 2020 KEY RESULTS: Impaired inhibition of IL-8 production by dexamethasone was detected in PBMCs from COPD patients and in CSE-exposed U937 cells, together with reduced levels of nuclear factor erythroid 2-related factor 2 (Nrf2) and histone deacetylase-2 (HDAC2). Dexamethasone 55-68 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 32335896-6 2020 In both PBMCs and CSE-exposed U937 cells, andrographolide restored dexamethasone inhibition of IL-8 production, accompanied by the up-regulation of Nrf2 and HDAC2 levels. andrographolide 42-57 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 32335896-6 2020 In both PBMCs and CSE-exposed U937 cells, andrographolide restored dexamethasone inhibition of IL-8 production, accompanied by the up-regulation of Nrf2 and HDAC2 levels. Dexamethasone 67-80 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 32464779-4 2020 Urinary metabolites of PAHs (i.e., OH-PAHs), measured as indicators of total PAH exposure, showed significant associations with markers of respiratory and systemic inflammation, including exhaled nitric oxide, interleukin (IL)-6 in exhaled breath condensate, and blood IL-2 and IL-8 levels and leucocyte count. oh-pahs 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 278-282 32464779-4 2020 Urinary metabolites of PAHs (i.e., OH-PAHs), measured as indicators of total PAH exposure, showed significant associations with markers of respiratory and systemic inflammation, including exhaled nitric oxide, interleukin (IL)-6 in exhaled breath condensate, and blood IL-2 and IL-8 levels and leucocyte count. Polycyclic Aromatic Hydrocarbons 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 278-282 32299619-1 2020 AIM: To analyse the relationship between 18F-labelled sodium fluoride (NaF) uptake and lumbar back pain in patients with lumbosacral transitional vertebra (LSTV) a congenital malformation of the lumbosacral spine. Sodium Fluoride 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 32543782-8 2020 RESULTS: The release of IL-8 was significantly increased after exposure to TEGDMA, Bis-GMA, UDMA, or TEGDMA in combination with Bis-GMA or UDMA compared to the unstimulated controls. Bisphenol A-Glycidyl Methacrylate 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 32299619-8 2020 The sensitivity and specificity of 18F-NaF uptake at LSTV as a cause of pain were 82% (95% confidence interval [CI]: 65-93%) and 86% (95% CI: 64-97%). lstv 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 32299619-10 2020 CONCLUSIONS: 18F-NaF PET/CT can be useful in evaluating back pain and 18F-NaF may be used as an adjunctive biological maker for assessing LSTV as a potential cause of pain. lstv 138-142 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 32543782-8 2020 RESULTS: The release of IL-8 was significantly increased after exposure to TEGDMA, Bis-GMA, UDMA, or TEGDMA in combination with Bis-GMA or UDMA compared to the unstimulated controls. urethane dimethacrylate luting resin 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 32543782-8 2020 RESULTS: The release of IL-8 was significantly increased after exposure to TEGDMA, Bis-GMA, UDMA, or TEGDMA in combination with Bis-GMA or UDMA compared to the unstimulated controls. triethylene glycol dimethacrylate 101-107 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 32543782-8 2020 RESULTS: The release of IL-8 was significantly increased after exposure to TEGDMA, Bis-GMA, UDMA, or TEGDMA in combination with Bis-GMA or UDMA compared to the unstimulated controls. urethane dimethacrylate luting resin 139-143 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 32543782-11 2020 CONCLUSION: The combination of TEGDMA and Bis-GMA had a synergistic proinflammatory effect on neutrophils by increasing the release of IL-8 and the formation of NET structures. triethylene glycol dimethacrylate 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 32543782-11 2020 CONCLUSION: The combination of TEGDMA and Bis-GMA had a synergistic proinflammatory effect on neutrophils by increasing the release of IL-8 and the formation of NET structures. Bisphenol A-Glycidyl Methacrylate 42-49 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 32342245-1 2020 18F-sodium fluoride (18F-NaF) has been used to access aortic stenosis in clinical research setting. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 32445015-12 2020 A significant increase in activation of NF-kappaB and production of pro-inflammatory cytokines IL-6 and IL-8 was observed after treatment with 4-HNE. 4-hydroxy-2-nonenal 143-148 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 31667675-2 2020 We sought to address this limitation by utilizing the distinctively high bone uptake rate constant Ki expected from 18F-Sodium Fluoride (18F-NaF) to segment bones from PET data and support 5-class hybrid PET/MR-driven AC for 18F-NaF and 18F-Fluorodeoxyglucose (18F-FDG) PET/MR cardiovascular imaging. Sodium Fluoride 116-135 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 32534189-4 2020 In vitro studies have demonstrated the capacity of azithromycin in reducing production of pro-inflammatory cytokines such as IL-8, IL-6, TNF alpha, reduce oxidative stress, and modulate T-helper functions. Azithromycin 51-63 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 32588186-10 2020 Namely, butyrate ameliorated the overproduction of adhesion molecules, including VCAM-1 and E-selectin, reduced oxidative stress by reducing the levels of ROS and 4-HNE, and suppressed inflammation via inhibition of MCP-1 and IL-8. Butyrates 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 32428523-1 2020 OBJECTIVES: The study aimed to compare the effectiveness of 38% silver diamine fluoride (SDF) solution, and 5% sodium fluoride (NaF) varnish applied semiannually in arresting dentin caries in young children with high caries risk. Sodium Fluoride 111-126 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 32531710-7 2020 C-BF and NFN treatment decreased (P < 0.05) IL-6, IL-8, IL-22, IL-10 and transforming growth factor-beta (TGF-beta) production in the jejunum and ileum compared with the control group. nfn 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 32752252-6 2020 Aesculetin inhibited alveolar epithelial induction of the mesenchymal markers in mCM-exposed/IL-8-loaded A549 cells ( 47-51% inhibition), while epithelial markers were induced in aesculetin-treated cells subject to mCM/IL-8 ( 1.5-2.3-fold induction). esculetin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 32382745-11 2020 NaF-EDTA plasma T Cavg for oral TU group was 403 +- 128 ng/dL (~14 +- 4 nmol/L; mean +- SD) [serum T equivalent ~ 489 +- 155 ng/dL (17 +- 5 nmol/L)] and for topical T was 391 +- 140 ng/dL (~14 +- 5 nmol/L). Edetic Acid 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 31667675-2 2020 We sought to address this limitation by utilizing the distinctively high bone uptake rate constant Ki expected from 18F-Sodium Fluoride (18F-NaF) to segment bones from PET data and support 5-class hybrid PET/MR-driven AC for 18F-NaF and 18F-Fluorodeoxyglucose (18F-FDG) PET/MR cardiovascular imaging. Fluorodeoxyglucose F18 237-259 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 31667675-2 2020 We sought to address this limitation by utilizing the distinctively high bone uptake rate constant Ki expected from 18F-Sodium Fluoride (18F-NaF) to segment bones from PET data and support 5-class hybrid PET/MR-driven AC for 18F-NaF and 18F-Fluorodeoxyglucose (18F-FDG) PET/MR cardiovascular imaging. Fluorodeoxyglucose F18 261-268 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 31667675-9 2020 In the R4:1 human cohort, the mean 18F-FDG:18F-NaF TBR increased by 12.2% at carotid bifurcations wall and 19.9% at vertebral bones. Fluorodeoxyglucose F18 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 32627003-0 2020 Molecular mechanism of gossypol mediating CCL2 and IL-8 attenuation in triple-negative breast cancer cells. Gossypol 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 33149453-3 2020 Hence, the aim and objective of the study was to assess and compare the root caries remineralization effect of plain milk, 5ppm of fluoridated milk, and 5ppm of NaF in deionized water. Water 178-183 C-X-C motif chemokine ligand 8 Homo sapiens 161-164 32487373-1 2020 In this study, we report the silver molybdate nanoparticles (beta-Ag2MoO4 NPs) based non-invasive and sensitive electrochemical immunosensor for label-free detection of Interleukin-8 (IL-8) biomarker. beta-ag2moo4 61-73 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 32487373-0 2020 Silver molybdate nanoparticles based immunosensor for the non-invasive detection of Interleukin-8 biomarker. Silver molybdate 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 32487373-1 2020 In this study, we report the silver molybdate nanoparticles (beta-Ag2MoO4 NPs) based non-invasive and sensitive electrochemical immunosensor for label-free detection of Interleukin-8 (IL-8) biomarker. Silver molybdate 29-45 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 32487373-1 2020 In this study, we report the silver molybdate nanoparticles (beta-Ag2MoO4 NPs) based non-invasive and sensitive electrochemical immunosensor for label-free detection of Interleukin-8 (IL-8) biomarker. Silver molybdate 29-45 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 32487373-1 2020 In this study, we report the silver molybdate nanoparticles (beta-Ag2MoO4 NPs) based non-invasive and sensitive electrochemical immunosensor for label-free detection of Interleukin-8 (IL-8) biomarker. beta-ag2moo4 61-73 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 31945773-9 2020 This molecule is developmentally functional in immature but not mature intestinal enterocytes; ILA reduces the interleukin-8 (IL-8) response after IL-1beta stimulus. indole-3-lactic acid 95-98 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 32311229-5 2020 Here, we examined the interaction between Ef.LTA and Pg.LPS on IL-8 induction in human periodontal ligament (PDL) cells. Leukotriene A4 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 32311229-5 2020 Here, we examined the interaction between Ef.LTA and Pg.LPS on IL-8 induction in human periodontal ligament (PDL) cells. pg 53-55 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 32311229-6 2020 Pg.LPS, but not Ef.LTA, induced IL-8 expression at both mRNA and protein levels, which was suppressed in the presence of Ef.LTA. pg 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 32311229-9 2020 Furthermore, Ef.LTA suppressed Pg.LPS-induced IL-8 promoter activity as well as AP-1, NF-IL6 and NF-kappaB transcription factors, which are indispensable for IL-8 expression. Leukotriene A4 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 32311229-9 2020 Furthermore, Ef.LTA suppressed Pg.LPS-induced IL-8 promoter activity as well as AP-1, NF-IL6 and NF-kappaB transcription factors, which are indispensable for IL-8 expression. Leukotriene A4 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 32311229-9 2020 Furthermore, Ef.LTA suppressed Pg.LPS-induced IL-8 promoter activity as well as AP-1, NF-IL6 and NF-kappaB transcription factors, which are indispensable for IL-8 expression. pg 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 32311229-9 2020 Furthermore, Ef.LTA suppressed Pg.LPS-induced IL-8 promoter activity as well as AP-1, NF-IL6 and NF-kappaB transcription factors, which are indispensable for IL-8 expression. pg 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 32311229-11 2020 In addition, silencing IRAK-M restored the decreased IL-8 expression by Ef.LTA in the presence of Pg.LPS. Leukotriene A4 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 32311229-11 2020 In addition, silencing IRAK-M restored the decreased IL-8 expression by Ef.LTA in the presence of Pg.LPS. pg 98-100 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 32311229-12 2020 Collectively, these results suggest that Ef.LTA inhibits Pg.LPS-induced IL-8 expression in human PDL cells via inducing the expression of a negative regulator of TLR signaling cascades, IRAK-M. pg 57-59 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 31945773-9 2020 This molecule is developmentally functional in immature but not mature intestinal enterocytes; ILA reduces the interleukin-8 (IL-8) response after IL-1beta stimulus. indole-3-lactic acid 95-98 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 32848840-12 2020 Inhibition of CFTR, significantly increased intracellular ROS and H2O2 levels over 30 min and significantly decreased Nrf2 expression by 70% while increasing SOD-2 expression over 24 h. CFTR siRNA significantly increased constitutive expression of IL-8 by HLMVECs. Hydrogen Peroxide 66-70 C-X-C motif chemokine ligand 8 Homo sapiens 248-252 32802081-12 2020 Atenolol increased IL-1RA in stroke-Mo and decreased IL-8 secretion from MSCs indicating an anti-inflammatory effect of atenolol on secretomes of these cells. Atenolol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 32802081-13 2020 Captopril increased IL-8 from stroke-Mo and increased IL-6, IL-8, and MCP-1 secretions from MSCs. Captopril 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 32802081-13 2020 Captopril increased IL-8 from stroke-Mo and increased IL-6, IL-8, and MCP-1 secretions from MSCs. Captopril 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 32802081-15 2020 Atenolol increased the secretion of IL-8 and MCP-1 while captopril increased the secretion of IL-6 and MCP-1 from MSCs. Atenolol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 32802081-17 2020 Losartan reduced MCP-1 and TNF-alpha from stroke-Mo and reduced IL-8 from cocultures of stroke-Mo and MSCs. Losartan 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 32727400-12 2020 Gene expression of the tumor-promoting cytokines and mediators, such as transforming growth factor (TGF)-beta1, vascular endothelial growth factor (VEGF), interleukin (IL)-8, and IL-6 were significantly suppressed by statins and zoledronic acid by up to 90% (p < 0.001). Zoledronic Acid 229-244 C-X-C motif chemokine ligand 8 Homo sapiens 155-173 32848840-15 2020 The effects of TNF-alpha and GlyH-101 on IL-8 expression were additive and inhibited by AG1478. N-(2-naphthalenyl)-((3,5-dibromo-2,4-dihydroxyphenyl)methylene)glycine hydrazide 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 32848840-15 2020 The effects of TNF-alpha and GlyH-101 on IL-8 expression were additive and inhibited by AG1478. RTKI cpd 88-94 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 32848840-17 2020 The antioxidant N-acetyl cysteine significantly reduced ROS production and the increase in IL-8 and VEGF expression following CFTR inhibition. Acetylcysteine 16-33 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 32792990-6 2020 In subsequent dose response studies, medroxyprogesterone acetate, but not progesterone, at doses of 10-6-10-8 M inhibited interleukin-1beta induced interleukin-8 and matrix metalloproteinase 1 mRNA expression. Medroxyprogesterone Acetate 37-64 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 32720061-0 2022 18F-NaF PET uptake characteristics of coronary artery culprit lesions in a cohort of patients of acute coronary syndrome with ST-elevation myocardial infarction and chronic stable angina: A hybrid fluoride PET/CTCA study. Fluorides 197-205 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 32792990-6 2020 In subsequent dose response studies, medroxyprogesterone acetate, but not progesterone, at doses of 10-6-10-8 M inhibited interleukin-1beta induced interleukin-8 and matrix metalloproteinase 1 mRNA expression. Progesterone 44-56 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 32792990-7 2020 We further demonstrated that inhibition of glucocorticoid receptor expression, but not progesterone receptor membrane component 1 knockdown with small interfering RNA transfection, resulted in a reversal in medroxyprogesterone acetate"s (10-7 M) inhibition of interleukin-1beta- induced matrix metalloproteinase 1 mRNA expression and interleukin-8 mRNA expression and protein expression. Medroxyprogesterone Acetate 207-234 C-X-C motif chemokine ligand 8 Homo sapiens 334-347 32694172-10 2020 Because increased IL-8 and CXCL1 production in tumors is associated with increased metastatic potential and cell seeding, poor prognosis, and enhanced recruitment of tumor-associated macrophages and fibroblasts, we propose that inhibition of host-cell binding and invasion, potentially through vaccination or novel galactoside compounds, could be an effective strategy for reducing F. nucleatum-associated CRC metastasis. Galactosides 315-326 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 33013263-0 2020 Development of a novel in vitro assay to evaluate environmental water using an IL-8 reporter cell line. Water 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 33013263-2 2020 Considering these characteristics, we examined the ability of the IL-8 luciferase assay using THP-G8 cells to evaluate water pollution. Water 119-124 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 33013263-9 2020 These data suggest the potential of the IL-8 luciferase assay for evaluating environmental water pollution both quantitatively and qualitatively. Water 91-96 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 32703950-3 2020 An intermediate liquid phase-Na2Mo2O7 is formed through a eutectic reaction of MoO3 and NaF, followed by being sulfurized into MoS2. na2mo2o7 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 32703950-3 2020 An intermediate liquid phase-Na2Mo2O7 is formed through a eutectic reaction of MoO3 and NaF, followed by being sulfurized into MoS2. mos2 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 32515977-8 2020 Among all the tested parameters, only ROS concentrations exhibited consistency with cell viability, and showed significant correlations with the expression levels of CYP1A1, HIF-1a, and especially with IL-8 (the marker for oxidative stress within the cell). Reactive Oxygen Species 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 32223225-5 2020 Our in vitro data demonstrate an increase in pro-inflammatory cytokines IL-6 and IL-8 levels in response to vaped PG and GLY exposures. Propylene Glycol 114-116 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 32223225-5 2020 Our in vitro data demonstrate an increase in pro-inflammatory cytokines IL-6 and IL-8 levels in response to vaped PG and GLY exposures. Glycerol 121-124 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 32685389-9 2020 Inhibiting ERK1/2 phosphorylation by LY3214996 reversed changes in VEGFR2 knockdown-induced IL-8 upregulation at the mRNA and the protein levels with no effects on cell viability. LY3214996 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 32601180-3 2020 We had shown that the peptide neurotensin (NT) is increased in the serum of children with ASD and stimulates cultured adult human microglia to secrete the proinflammatory molecules IL-1beta and CXCL8. Peptides 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 194-199 32676905-1 2021 BACKGROUND: Increased uptake of 18F-Sodium fluoride (18F-NaF) PET has potential to identify atherosclerotic plaques that are vulnerable to rupture. 18f-sodium fluoride 32-51 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 32708494-8 2020 SCFAs (except hexanoic acid) increased ApoA-I mRNA transcription in both normal and inflammatory conditions and lowered IL-8 mRNA expression. hexanoic acid 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 31036393-11 2020 CONCLUSION: Plant derived essential oils and related active compounds have potential therapeutic activity for the treatment of asthma by modulating the release of pro-inflammatory (TNF-alpha, IL-1beta, IL-8), Th17 (IL-17), anti-inflammatory (IL-10), Th1 (IFN-gamma, IL-2, IL-12) and Th2 (IL-4, IL-5, IL-6, IL-13) cytokines and the suppression of inflammatory cell accumulation. Oils, Volatile 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 32674502-6 2020 In addition, PCG significantly decreased PAR2-induced increases in ICAM-1 and VCAM-1 as well as in IL-8, IFN-gamma, and TNF-alpha expression. punicalagin 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 32510220-8 2020 However, concentrations of PFOS and 6:2 Cl-PFESA were both significantly and positively associated with MCP-1 levels, while PFOA was inversely associated with IL-8. perfluorooctanoic acid 124-128 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 32238729-4 2020 Administration of steroid and high-dose intravenous immunoglobulin (1 g/kg) did not alleviate fever or reduce cytokine production; however, after administration of etoposide (an antineoplastic agent), fever decreased immediately, the patient"s general condition improved, and levels of IL-6, IL-10, IL-8, MCP-1, IFN-gamma, and TNF-alpha declined after etoposide administration. Etoposide 164-173 C-X-C motif chemokine ligand 8 Homo sapiens 299-303 32615949-10 2020 CONCLUSION: Collectively, the unique mechanism of etoposide with G-CSF-induced mobilization is associated with IL-8 secretion from the BMSCs, which is responsible for the enhanced proliferation and mobilization of HSCs in the bone marrow; this was not observed with mobilization using cyclophosphamide with G-CSF or G-CSF alone. Etoposide 50-59 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 32684872-0 2020 Tritiated Water Induces Toxicity in Human Umbilical Vein Vascular Endothelial Cells via IL8. Water 10-15 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 32615949-10 2020 CONCLUSION: Collectively, the unique mechanism of etoposide with G-CSF-induced mobilization is associated with IL-8 secretion from the BMSCs, which is responsible for the enhanced proliferation and mobilization of HSCs in the bone marrow; this was not observed with mobilization using cyclophosphamide with G-CSF or G-CSF alone. Cyclophosphamide 285-301 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 32615949-0 2020 Etoposide-mediated interleukin-8 secretion from bone marrow stromal cells induces hematopoietic stem cell mobilization. Etoposide 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 32608284-0 2020 Up-regulation of miR-20a weakens inflammation and apoptosis in high-glucose-induced renal tubular cell mediating diabetic kidney disease by repressing CXCL8 expression. Glucose 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 151-156 32615949-6 2020 In in vitro experiments, etoposide triggered interleukin (IL)-8 secretion from the BMSCs and caused long-term BMSC toxicity. Etoposide 25-34 C-X-C motif chemokine ligand 8 Homo sapiens 45-63 32615949-9 2020 In animal studies, the etoposide with G-CSF mobilization group presented higher IL-8-related cytokine and MMP9 expression and lower SDF-1 expression in the BM, compared to the groups not treated with etoposide. Etoposide 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 32661687-13 2020 In contrast, TiO2 significantly decreased cell viability and increased interleukin-8 release in fibroblast monolayers. titanium dioxide 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 32375543-0 2020 18F-Sodium Fluoride (18F-NaF) for Imaging Microcalcification Activity in the Cardiovascular System. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 32375543-2 2020 Calcification activity can now be imaged using 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) in combination with either computed tomography or magnetic resonance. 18f-sodium fluoride 47-66 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 31734781-1 2020 AIMS: To investigate the benefit of utilizing 18F-sodium fluoride (NaF) PET/CT over calcium and Framingham scoring for potential preventative coronary artery disease (CAD) intervention. Sodium Fluoride 46-65 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 32388485-8 2020 Notably, longifolioside A disrupted the interaction between human TLR4 and the TIR domain-containing adaptor protein (TIRAP), an early step during TLR4 activation, thereby reducing IL-8 secretion in 293/HA-hTLR4 cells. Longifolioside A 9-25 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 31786626-6 2020 18F-fluorodeoxyglucose (FDG) (49/53) and 18F-sodium fluoride (NaF) (5/53) were the most utilized tracers to visualize carotid wall inflammation and microcalcification, respectively. Sodium Fluoride 41-60 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 32141941-6 2020 RESULTS: Pretreatment with 10 M DHT or 17-beta-estradiol inhibited the high osmolarity-induced expression of TNF-alpha, IL-8, and IL-6. Dihydrotestosterone 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 32141941-6 2020 RESULTS: Pretreatment with 10 M DHT or 17-beta-estradiol inhibited the high osmolarity-induced expression of TNF-alpha, IL-8, and IL-6. Estradiol 39-56 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 32352600-0 2020 The association between interleukin-8 levels and the development of withdrawal symptoms during methamphetamine abstinence. Methamphetamine 95-110 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 32550884-7 2020 Furthermore, icariin significantly increased protein expression of the anti-inflammatory factor interleukin (IL)-10 and significantly decreased protein expression of the pro-inflammatory factors IL-8 and tumor necrosis factor alpha. icariin 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 31897585-1 2020 PURPOSE: 18F-Sodium fluoride (18F-NaF) positron emission tomography (PET) has the potential to detect high-risk coronary plaques. 18f-sodium fluoride 9-28 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 31897585-8 2020 Focal 18F-NaF uptake in each plaque was quantified using the maximum tissue-to-background ratio (TBRmax). tbrmax 97-103 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 31897586-1 2020 PURPOSE: 18F-sodium fluoride (18F-NaF) has shown promise in assessing disease activity in coronary arteries, but currently used measures of activity - such as maximum target to background ratio (TBRmax) - are defined by single pixel count values. 18f-sodium fluoride 9-28 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 32352600-8 2020 Serum IL-8 levels remained associated with the severity of METH withdrawal symptoms (beta = .363, p = .023), after adjusting for potential confounders. Methamphetamine 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 32352600-13 2020 CONCLUSIONS: Our study demonstrated that higher serum IL-8 levels may predict more severe withdrawal symptoms at 2 weeks after METH abstinence. Methamphetamine 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 31629684-1 2020 PURPOSE: This study aimed to elucidate the effects of hydrogen peroxide (H2O2) and sodium fluoride (NaF) on titanium surfaces under conditions mimicking those encountered during dental treatment. Sodium Fluoride 83-98 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 32361568-9 2020 DMSO-HL and ATRA-HL cells both produced TNF-alpha and IL-8 after lipopolysaccharide (LPS) or PM treatment, whereas non-differentiated HL-60 cells did not. Tretinoin 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 33149400-4 2020 They were allocated to group I (GI) (5% NaF), group II (GII) [5% NaF with amorphous calcium phosphate (ACP)], and group III (GIII) [5% NaF with casein phosphopeptides - amorphous calcium phosphate (CPP -ACP)]. amorphous 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 33149400-4 2020 They were allocated to group I (GI) (5% NaF), group II (GII) [5% NaF with amorphous calcium phosphate (ACP)], and group III (GIII) [5% NaF with casein phosphopeptides - amorphous calcium phosphate (CPP -ACP)]. amorphous 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 33149400-4 2020 They were allocated to group I (GI) (5% NaF), group II (GII) [5% NaF with amorphous calcium phosphate (ACP)], and group III (GIII) [5% NaF with casein phosphopeptides - amorphous calcium phosphate (CPP -ACP)]. amorphous calcium phosphate 74-101 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 33149400-4 2020 They were allocated to group I (GI) (5% NaF), group II (GII) [5% NaF with amorphous calcium phosphate (ACP)], and group III (GIII) [5% NaF with casein phosphopeptides - amorphous calcium phosphate (CPP -ACP)]. amorphous calcium phosphate 74-101 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 32380135-13 2020 CONCLUSIONS: Dab-on with NaF and SnF2 or brushing with SnF2 reduces DH in eroded dentine. diazobenzenesulfonic acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 31629684-1 2020 PURPOSE: This study aimed to elucidate the effects of hydrogen peroxide (H2O2) and sodium fluoride (NaF) on titanium surfaces under conditions mimicking those encountered during dental treatment. Titanium 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 32377746-8 2020 It was also demonstrated that DHMEQ exposure significantly decreased the levels of interleukin (IL)-8 and monocyte chemoattractant protein-1 (MCP-1) in the supernatant of cultured ARPE-19 cells as determined by ELISA. dehydroxymethylepoxyquinomicin 30-35 C-X-C motif chemokine ligand 8 Homo sapiens 83-101 31773201-13 2020 In addition, ISB with DEX showed lower mean plasma IL-6 and IL-8 levels than ISB alone within 48 h postoperatively, with delayed rebound pain. Dexmedetomidine 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 32030555-10 2020 After 10 days, compared to after 5 days, a reduced tissue loss was observed in all groups treated with AmF/NaF/SnCl2 solution. stannous chloride 111-116 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 32030555-12 2020 Short-pulsed CO2 9.3 mum laser irradiation followed by additional application of AmF/NaF/SnCl2 solution significantly reduces the progression of dental enamel erosion in vitro. Amphotericin B 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 32030555-12 2020 Short-pulsed CO2 9.3 mum laser irradiation followed by additional application of AmF/NaF/SnCl2 solution significantly reduces the progression of dental enamel erosion in vitro. stannous chloride 89-94 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 32377746-9 2020 Moreover, the protein expression levels of IL-8 and MCP-1 were significantly reduced in ARPE-19 cells exposed to DHMEQ compared with cells exposed to dexamethasone. dehydroxymethylepoxyquinomicin 113-118 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 32377746-9 2020 Moreover, the protein expression levels of IL-8 and MCP-1 were significantly reduced in ARPE-19 cells exposed to DHMEQ compared with cells exposed to dexamethasone. Dexamethasone 150-163 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 32490857-6 2020 The polyphenols and their microbial metabolites alleviate IBD through reduction of oxidative stress, inhibition of inflammatory cytokines secretion (TNF-alpha, IL-6, IL-8, and IL-1beta), suppression of NF-kappaB, upregulation of Nrf2, gut barrier protection, and modulation of immune function. Polyphenols 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 32452426-0 2020 Glibenclamide alters interleukin-8 and interleukin-1beta of primary human monocytes from diabetes patients against Mycobacterium tuberculosis infection. Glyburide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 32452426-2 2020 Our previous study showed glibenclamide, an anti-diabetic drug used to control blood glucose concentration, reduced interleukin (IL)-8 secretion from primary human monocytes challenged with M. tuberculosis (Mtb). Glyburide 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 116-134 32452426-6 2020 We demonstrate that monocytes from diabetes patients who were being treated with glibenclamide showed reduced IL-1beta and IL-8 secretion when exposed to Mtb. Glyburide 81-94 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 32452426-9 2020 Taken together, our data show that glibenclamide might exacerbate susceptibility of diabetes patients to Mtb infection by reducing IL-1beta and IL-8 production by monocytes. Glyburide 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 32605011-0 2020 In Vitro and In Vivo Assessment of PEGylated PEI for Anti-IL-8/CxCL-1 siRNA Delivery to the Lungs. pegylated pei 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 32573468-9 2020 Higher stability of remdesivir and metabolite was observed on NaF-plasma. remdesivir 20-30 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 32553260-2 2020 Coronary 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) provides an assessment of atherosclerosis activity. 18f-sodium fluoride 9-28 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 32685267-1 2020 BACKGROUND: We used 18F-sodium fluoride (NaF) to assess early atherosclerosis in the global heart in asymptomatic individuals with a coronary calcium score of zero and without a formal diagnosis of hypertension. 18f-sodium fluoride 20-39 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 32564053-7 2020 RESULTS Compared with the healthy controls, the serum expression of IL-18, IL-33, IFN-gamma, IL-5, IL-6, IL-8, and IL-13 were significantly higher in the MPP and NMPP groups. nmpp 162-166 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 32569211-4 2020 Meanwhile, MIR103 and MIR107 were negatively correlated with acute pathologic and chronic health evaluation (APACHE) II score, sequential organ failure assessment (SOFA) score, serum creatinine, C-reactive protein, tumor necrosis factor, interleukin 1beta, interleukin 6 and interleukin 8, while positively correlated with albumin in sepsis patients. mir103 11-17 C-X-C motif chemokine ligand 8 Homo sapiens 275-288 32570911-6 2020 RESULTS: Our data showed that ZnO was able to reduce the inflammatory response of DECs, in terms of vascular cell adhesion molecule-1 (VCAM-1), interleukin (IL)-8, IL-6, tumor necrosis factor-alpha (TNF-alpha) and monocyte chemoattractant protein-1 (MCP-1) expression induced by TNF-alpha stimulation. Zinc Oxide 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 144-162 32676215-0 2020 Interleukin-8 in Hyperlipidemia and Coronary Heart Disease in Thai Patients Taking Statin Cholesterol-Lowering Medication While Undergoing Coronary Artery Bypass Grafting Treatment. statin cholesterol 83-101 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 32676215-2 2020 This cross-sectional study investigates the association of the IL-8 expression in hyperlipidemia (H) and CHD patients who have been treated with statin cholesterol-lowering drugs while undergoing coronary artery bypass grafting treatment. Cholesterol 152-163 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 32595508-4 2020 A dichloromethane extract (OS1), mainly composed of isoflavonoids and triterpenes as characterized by LC-MS, showed a concentration-dependent (25-100 mug/ml) inhibition of IL-8 and TNF-alpha release from LPS-stimulated human neutrophils. Methylene Chloride 2-17 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 31759072-0 2020 Acute alcohol consumption alters the peripheral cytokines IL-8 and TNF-alpha. Alcohols 6-13 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 32545315-1 2020 The study aimed to analyze morphological and functional changes of Staphylococcus aureus cells due to trans-anethole (a terpenoid and the major constituent of fennel, anise, or star anise essential oils) exposition, and their consequences for human neutrophils phagocytic activity as well as IL-8 production (recognized as the major chemoattractant). anethole 102-116 C-X-C motif chemokine ligand 8 Homo sapiens 292-296 32545315-7 2020 Additionally, IL-8 production was at a higher level for trans-anethole modified bacteria. anethole 56-70 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 32551386-6 2020 NAC-related increase in glutathione was associated with significant alterations in tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-6, IL-8 and IL-10 levels secreted in the culture medium. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 32551386-6 2020 NAC-related increase in glutathione was associated with significant alterations in tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-6, IL-8 and IL-10 levels secreted in the culture medium. Glutathione 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 32551386-7 2020 A substantial decrease in the IL-6, IL-8 and TNF-alpha levels in the culture medium supplemented with NAC was obvious in hepatocytes recovered 14 days after differentiation. Acetylcysteine 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 32595508-4 2020 A dichloromethane extract (OS1), mainly composed of isoflavonoids and triterpenes as characterized by LC-MS, showed a concentration-dependent (25-100 mug/ml) inhibition of IL-8 and TNF-alpha release from LPS-stimulated human neutrophils. Triterpenes 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 31759072-7 2020 RESULTS: The pro-inflammatory chemokine IL-8 significantly increased 6 hours after alcohol (F(1,34)=4.13, p=0.0002, d"=0.5). Alcohols 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 31759072-10 2020 CONCLUSIONS: In our exploratory data, acute alcohol challenge (120 mg/dL) elicits dynamic changes in the pro-inflammatory molecules IL-8 and TNF-alpha. Alcohols 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 33911737-6 2020 Results: Interleukin-8 (IL-8) and tumor necrosis factor (TNF)-alpha release was suppressed when keratinocytes were co-treated with oligo-HAs and LL-37 compared with keratinocytes treated with LL-37 only. Oligosaccharides 131-140 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 33911737-6 2020 Results: Interleukin-8 (IL-8) and tumor necrosis factor (TNF)-alpha release was suppressed when keratinocytes were co-treated with oligo-HAs and LL-37 compared with keratinocytes treated with LL-37 only. Oligosaccharides 131-140 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 32028158-6 2020 Phosphorus transformed from water-soluble phosphorus (Ca(H2PO4)2, Ca(HPO4)) into insoluble Ca3(PO4)2.20 reducing-oxidizing cycles were investigated, and a less and less fluorine content in oxygen carrier was found because its phase transformation from solid NaF to gaseous HF, and the phosphorus content in oxygen carrier changed slightly under the current conditions. Phosphorus 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 258-261 31840936-12 2020 Metformin or AICAR presence decreased spontaneous production of IL-6, IL-8 and MCP-1 in RA synovial explants and SFCs (n=5-7). Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 31840936-12 2020 Metformin or AICAR presence decreased spontaneous production of IL-6, IL-8 and MCP-1 in RA synovial explants and SFCs (n=5-7). AICA ribonucleotide 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 32058033-9 2020 EPA and DHA also significantly lowered production of monocyte chemoattractant protein 1, interleukin (IL)-6 and IL-8. Eicosapentaenoic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 32058033-9 2020 EPA and DHA also significantly lowered production of monocyte chemoattractant protein 1, interleukin (IL)-6 and IL-8. Docosahexaenoic Acids 8-11 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 32361849-8 2020 CXCL8 level was significantly upgraded after NAC in CXCR1/2+ patients and downgraded after NAC in CXCR1/2- patients. nac 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 32361849-8 2020 CXCL8 level was significantly upgraded after NAC in CXCR1/2+ patients and downgraded after NAC in CXCR1/2- patients. nac 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 32361849-13 2020 The CXCL8-CXCR1/2 might play an important role in tailoring and modifying the NAC strategy for advanced TNBCs; however, further confirmatory studies are needed. nac 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 4-9 32286869-15 2020 Fluorine-18-labeled NaF PET/CT showed axial bone lesions with bone formation and can be used as a monitoring tool in patients with AS receiving anti-TNF-alpha drugs. Fluorine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 32088457-5 2020 30% RM converted water-soluble NaF into more stable CaF2 than did SPL at 850 C, thus reducing the leaching rate by 45.15%. Water 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 32602468-10 2020 At the T1D onset, the concentrations of Fetuin-A (p=0.031) and IL-8 (p=0.042) were significantly higher in patients compared to those without CPR. cpr 142-145 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 32088457-8 2020 SiO2 and Al2O3 exerted a thermally positive effect on NaF turning into CaF2. Silicon Dioxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 32088457-8 2020 SiO2 and Al2O3 exerted a thermally positive effect on NaF turning into CaF2. Aluminum Oxide 9-14 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 32088457-9 2020 The fluoride retention of the bottom ash was mainly dominated by CaF2 and NaF with(out) RM. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 32199215-3 2020 Our study showed that treating human bronchial epithelial (16HBE) cells with neodymium oxide caused an inflammatory response by upregulating the expression of interleukin-8 (IL-8) and interleukin-1 beta (IL-1beta). neodymium oxide 77-92 C-X-C motif chemokine ligand 8 Homo sapiens 159-172 32199215-3 2020 Our study showed that treating human bronchial epithelial (16HBE) cells with neodymium oxide caused an inflammatory response by upregulating the expression of interleukin-8 (IL-8) and interleukin-1 beta (IL-1beta). neodymium oxide 77-92 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 32199215-7 2020 Moreover, circ_0000638 reduced the expression of IL-8 and IL-1beta by inhibiting NF-kappaB activation in neodymium oxide-treated 16HBE cells. circ_0000638 10-22 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 32199215-7 2020 Moreover, circ_0000638 reduced the expression of IL-8 and IL-1beta by inhibiting NF-kappaB activation in neodymium oxide-treated 16HBE cells. neodymium oxide 105-120 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 32199215-7 2020 Moreover, circ_0000638 reduced the expression of IL-8 and IL-1beta by inhibiting NF-kappaB activation in neodymium oxide-treated 16HBE cells. 16hbe 129-134 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 32199215-8 2020 These results suggest that circ_0000638 can inhibit NF-kappaB activation by competitively binding to miR-498-5p, further downregulating the expression of IL-8 and IL-1beta in neodymium oxide-treated 16HBE cells. circ_0000638 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 32199215-8 2020 These results suggest that circ_0000638 can inhibit NF-kappaB activation by competitively binding to miR-498-5p, further downregulating the expression of IL-8 and IL-1beta in neodymium oxide-treated 16HBE cells. neodymium oxide 175-190 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 32199215-8 2020 These results suggest that circ_0000638 can inhibit NF-kappaB activation by competitively binding to miR-498-5p, further downregulating the expression of IL-8 and IL-1beta in neodymium oxide-treated 16HBE cells. 16hbe 199-204 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 31609478-8 2020 Gene expression analysis in PDAC tumors (n = 63) showed a positive correlation between the expression of NOS2 and the tryptophan/kynurenine pathway genes, including indoleamine-2,3-dioxygenase 1 (IDO1) and several aryl hydrocarbon receptor (AHR)-target genes including NFE2L2 (NRF2), SERPINB2, IL1b, IL6 and IL8, which are implicated in pancreatic cancer. Kynurenine 129-139 C-X-C motif chemokine ligand 8 Homo sapiens 308-311 32179246-4 2020 Our results indicate that alogliptin treatment ameliorated IL-1beta-induced production of reactive oxygen species, the expression of matrix metalloproteinase-3 (MMP-3) and MMP-13, secretions of tumor necrosis factor-alpha (TNF-alpha), IL-6, and IL-8. alogliptin 26-36 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 31773235-1 2020 PURPOSE: We examined the literature to elucidate the role of 18F-sodium fluoride (NaF)-PET in atherosclerosis. Sodium Fluoride 61-80 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 31925623-3 2020 The results showed that THP-1 cells, which were stimulated by LAMPs after pretreatment with H2S, had decreased production of interleukin-6 (IL-6) and interleukin-8 (IL-8) by inhibiting the mitogen-activated protein kinases (MAPKs)/nuclear factor-kappa B (NF-kappaB) signaling pathway and increased expression of HO-1 by activating the nuclear factor E2-related factor 2 (Nrf2) signaling pathway. hydrogen sulfite 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 31925623-3 2020 The results showed that THP-1 cells, which were stimulated by LAMPs after pretreatment with H2S, had decreased production of interleukin-6 (IL-6) and interleukin-8 (IL-8) by inhibiting the mitogen-activated protein kinases (MAPKs)/nuclear factor-kappa B (NF-kappaB) signaling pathway and increased expression of HO-1 by activating the nuclear factor E2-related factor 2 (Nrf2) signaling pathway. hydrogen sulfite 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 31925623-4 2020 Our results indicate that H2S may play an important role in attenuating inflammation induced by M. pneumoniae LAMPs due to its ability to decrease the production of IL-6 and IL-8 and increase the expression of the HO-1. hydrogen sulfite 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 32602468-11 2020 CONCLUSION: Evaluation of Fetuin-A and IL-8 levels in patients with a newly diagnosed T1D can differentiate between patients with or without CPR. cpr 141-144 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 32431334-3 2020 CPH digests significantly inhibited the expression of cyclooxygenase-2 and inducible nitric oxide synthase, and reduced the secretion of interleukin-8 in TNF-alpha-induced inflammation in Caco-2 cells. cph 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 137-150 32037273-11 2020 Methylprednisolone reduced the proinflammatory cytokines interleukin-6 and interleukin-8 and increased the anti-inflammatory cytokine interleukin-10 postoperatively. Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 75-88 32374474-5 2020 In the present study, silvestrol down-regulated several pro- and anti-inflammatory cytokines (IL-6, IL-8, IL-10, CCL2, CCL18) and increased TNF-alpha during differentiation and activation of M1-macrophages, suggesting that the effects of silvestrol might cancel each other out. silvestrol 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 32374474-6 2020 However, silvestrol amplified the anti-inflammatory potential of M2-macrophages by increasing expression of anti-inflammatory surface markers CD206, TREM2 and reducing release of pro-inflammatory IL-8 and CCL2. silvestrol 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 32589092-5 2020 Moreover, AZM can inhibit the ability of TNF-alpha-to induce interleukin (IL)-8 production. Azithromycin 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 61-79 32589092-6 2020 This review focuses on the effects on AZM that may be beneficial in inhibiting MUC5AC, matrix metalloprotease-9 and IL-8 production in airway epithelial cells. Azithromycin 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 32179074-3 2020 KEY FINDINGS: Pre-treatment with quercetin significantly reversed the LPS-induced upregulation of pro-fibrotic factors (IL-6, IL-8, COL-1, COL-3, LC3) and fibrotic signaling mediators (mTOR and AKT), and it induced the downregulation of ATG5 in the WI-38 cells. Quercetin 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 32069432-6 2020 MCP-1 and GM-CSF levels, as well as gene expressions of IL-6 and IL-8 in HTR8/SVneo cells were greatly increased by TNF-alpha (5, 10 and 20 ng/mL), but reversed by sevoflurane and SB203580. sevoflurane 164-175 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 32069432-6 2020 MCP-1 and GM-CSF levels, as well as gene expressions of IL-6 and IL-8 in HTR8/SVneo cells were greatly increased by TNF-alpha (5, 10 and 20 ng/mL), but reversed by sevoflurane and SB203580. SB 203580 180-188 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 30684262-1 2020 INTRODUCTION: 18F-Sodium Fluoride Positron Emission Tomography (18F-NaF PET) is a novel molecular imaging modality with promise for use as a risk stratification tool in cardiovascular disease. 18f-sodium fluoride 14-33 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 32219875-7 2020 DSR-6434 triggered 20-fold lower levels of IFN-alpha by pDCs, but higher production of IL-6, IL-8 and TNF, compared to RNA-IC. DSR-6434 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 31833613-8 2020 Diosmetin treatment resulted in an increase in apoptotic rates and a reduction in TNF-alpha-induced production of IL-1beta, IL-6, IL-8, and MMP-1 in MH7A cells. diosmetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 32483313-5 2020 Increased cytokines IL-6 as well as IL-8 were released by resistant cells, along with increased mammospheres and induction of EMT, all of which was inhibited by propofol. Propofol 161-169 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 32615160-12 2020 In addition, combining bergenin and dexamethasone (DEX) yielded additive effects on the reduction of IL-6 and IL-8 expression. bergenin 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 32615160-12 2020 In addition, combining bergenin and dexamethasone (DEX) yielded additive effects on the reduction of IL-6 and IL-8 expression. Dexamethasone 36-49 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 32615160-12 2020 In addition, combining bergenin and dexamethasone (DEX) yielded additive effects on the reduction of IL-6 and IL-8 expression. Dexamethasone 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 32596498-8 2020 IL-8 and TNF-alpha cytokines showed milder increases of DAPI, MPO, and CitH3 positive cells. DAPI 56-60 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 32062016-0 2020 Soluble silver ions from silver nanoparticles induce a polarised secretion of interleukin-8 in differentiated Caco-2 cells. Silver 8-14 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 32062016-0 2020 Soluble silver ions from silver nanoparticles induce a polarised secretion of interleukin-8 in differentiated Caco-2 cells. Silver 25-31 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 32062016-4 2020 In this context, the present study aims at assessing the impact of silver nanoparticles on the secretion of the pro-inflammatory chemokine interleukin-8 by Caco-2 cells forming an in vitro model of the intestinal mucosal barrier. Silver 67-73 C-X-C motif chemokine ligand 8 Homo sapiens 139-152 32062016-5 2020 Silver nanoparticles induced a vectorized secretion of interleukin-8 towards the apical compartment, which is found in the medium 21 hours after the incubation. Silver 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 32062016-7 2020 The soluble silver fraction of silver nanoparticles suspensions led to a similar amount of secreted interleukin-8 than silver nanoparticles, suggesting an involvement of silver ions in this interleukin-8 secretion. Silver 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 32062016-7 2020 The soluble silver fraction of silver nanoparticles suspensions led to a similar amount of secreted interleukin-8 than silver nanoparticles, suggesting an involvement of silver ions in this interleukin-8 secretion. Silver 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 190-203 32062016-7 2020 The soluble silver fraction of silver nanoparticles suspensions led to a similar amount of secreted interleukin-8 than silver nanoparticles, suggesting an involvement of silver ions in this interleukin-8 secretion. Silver 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 32062016-7 2020 The soluble silver fraction of silver nanoparticles suspensions led to a similar amount of secreted interleukin-8 than silver nanoparticles, suggesting an involvement of silver ions in this interleukin-8 secretion. Silver 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 190-203 32062016-7 2020 The soluble silver fraction of silver nanoparticles suspensions led to a similar amount of secreted interleukin-8 than silver nanoparticles, suggesting an involvement of silver ions in this interleukin-8 secretion. Silver 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 32062016-7 2020 The soluble silver fraction of silver nanoparticles suspensions led to a similar amount of secreted interleukin-8 than silver nanoparticles, suggesting an involvement of silver ions in this interleukin-8 secretion. Silver 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 190-203 32062016-7 2020 The soluble silver fraction of silver nanoparticles suspensions led to a similar amount of secreted interleukin-8 than silver nanoparticles, suggesting an involvement of silver ions in this interleukin-8 secretion. Silver 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 32062016-7 2020 The soluble silver fraction of silver nanoparticles suspensions led to a similar amount of secreted interleukin-8 than silver nanoparticles, suggesting an involvement of silver ions in this interleukin-8 secretion. Silver 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 190-203 32469940-4 2020 In the present study carried out in whole blood, heparin and selectively desulfated heparin reduced histone induced inflammatory markers such as interleukin 6 (IL 6), interleukin 8 (IL 8) and tissue factor and C3a, a complement component. Heparin 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 32469940-4 2020 In the present study carried out in whole blood, heparin and selectively desulfated heparin reduced histone induced inflammatory markers such as interleukin 6 (IL 6), interleukin 8 (IL 8) and tissue factor and C3a, a complement component. Heparin 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 32469940-4 2020 In the present study carried out in whole blood, heparin and selectively desulfated heparin reduced histone induced inflammatory markers such as interleukin 6 (IL 6), interleukin 8 (IL 8) and tissue factor and C3a, a complement component. Heparin 84-91 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 32469940-4 2020 In the present study carried out in whole blood, heparin and selectively desulfated heparin reduced histone induced inflammatory markers such as interleukin 6 (IL 6), interleukin 8 (IL 8) and tissue factor and C3a, a complement component. Heparin 84-91 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 32456181-2 2020 Sodium fluoride (18F-NaF) is a highly sensitive tracer of bone reconstruction, evolving as an important imaging agent for the assessment of malignant bone diseases. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 32509050-9 2020 The IL-8 level was suppressed more significantly by quercetin metabolites in the perfusion co-culture, as compared to static culture. Quercetin 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 32466509-9 2020 Our study indicates that 17-aminogeldanamycin can be used for efficient inhibition of NF-kappaB activity and the simultaneous diminution of IL-8 and VEGF levels in the extracellular milieu of melanoma. 17-aminogeldanamycin 25-45 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 32319286-9 2020 Exposure of differentiated Caco-2 cells to positively or negatively surface-charged SiO2 NPs also upregulated interleukin-8 expression. Silicon Dioxide 84-88 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 31770582-6 2020 The dexamethasone (Dex) concentration required to achieve 50% inhibition of TNF-alpha-induced interleukin (IL)-8 production was determined and the mitogen-activated protein kinase (MAPK)/Activator protein-1 (AP-1) pathway was also evaluated. Dexamethasone 4-17 C-X-C motif chemokine ligand 8 Homo sapiens 94-112 31770582-6 2020 The dexamethasone (Dex) concentration required to achieve 50% inhibition of TNF-alpha-induced interleukin (IL)-8 production was determined and the mitogen-activated protein kinase (MAPK)/Activator protein-1 (AP-1) pathway was also evaluated. Dexamethasone 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 94-112 32481266-9 2020 Meanwhile, the area under the curve (AUC) of IL-8 in EBC was significantly lower at T2 and the AUC of IL-6 in EBC was significantly higher at T4 than in serum (P < .05). NSC638702 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 32434541-11 2020 Cisplatin but not erlotinib increased both IL-6 and IL-8 secretion and only IL-6 increased cellular migration and proliferation. Cisplatin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 32418407-7 2020 RESULTS: Results obtained in this work demonstrated that CKG is able to prevent the impairment of intestinal barrier function induced by inflammation, ameliorating the transepithelial electrical resistance and the paracellular permeability of the Caco-2 monolayer; moreover, CKG is able to counteract the increased release of TNF-a and IL-8 induced by inflammatory stimulus, thus reducing the intestinal inflammation. CHEMBL1171949 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 336-340 32414118-7 2020 Consequentially, resveratrol reduced PM-induced cyclooxygenase-2/prostaglandin E2 and proinflammatory cytokine expression, including that of matrix metalloproteinase (MMP)-1, MMP-9, and interleukin-8, all of which are known to be central mediators of various inflammatory conditions and aging. Resveratrol 17-28 C-X-C motif chemokine ligand 8 Homo sapiens 186-199 32494176-11 2020 Furthermore, deficient 25(OH)D individuals with low HDL-C levels had higher circulatory IL-6 and IL-8 levels, and higher serum soluble TM compared to individuals with sufficient 25(OH)D and normal lipid profiles (median, IL-6 pg/mL 0.82 vs 1.71, P=0.001; median, IL-8 pg/mL 51.31 vs 145.6, P=0.003; and median, soluble TM ng/mL 5.19 vs 7.38, P<0.0001; in sufficient vs deficient groups, respectively). 25(oh)d 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 32494176-11 2020 Furthermore, deficient 25(OH)D individuals with low HDL-C levels had higher circulatory IL-6 and IL-8 levels, and higher serum soluble TM compared to individuals with sufficient 25(OH)D and normal lipid profiles (median, IL-6 pg/mL 0.82 vs 1.71, P=0.001; median, IL-8 pg/mL 51.31 vs 145.6, P=0.003; and median, soluble TM ng/mL 5.19 vs 7.38, P<0.0001; in sufficient vs deficient groups, respectively). 25(oh)d 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 263-267 32370749-10 2020 Meanwhile, sinensetin treatment significantly decreased IAV-induced expression of pro-inflammatory mediators at mRNA and protein levels, including IL-6, TNF-alpha, IP-10, IL-8 and MCP-1. sinensetin 11-21 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 32397252-2 2020 Our aim was to quantify vascular calcification in the arteries and the deposition of 18F-sodium-fluoride (18F-NaF) in the skin and vessel walls with positron emission tomography/computed tomography. 18f-sodium-fluoride 85-104 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 32440119-1 2020 Objectives: The first objective of this study was to prepare sodium fluoride (NaF) solution with various concentrations of polyethylene glycol-coated silver nanoparticles (PEG-AgNPs). Sodium Fluoride 61-76 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 32440119-1 2020 Objectives: The first objective of this study was to prepare sodium fluoride (NaF) solution with various concentrations of polyethylene glycol-coated silver nanoparticles (PEG-AgNPs). polyethylene glycol-coated silver nanoparticles 123-170 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 32440119-1 2020 Objectives: The first objective of this study was to prepare sodium fluoride (NaF) solution with various concentrations of polyethylene glycol-coated silver nanoparticles (PEG-AgNPs). peg-agnps 172-181 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 32440119-6 2020 The staining effect on dentin and enamel for the 2.5% NaF solutions with PEG-AgNPs at 12,800, 6400, 1600, and 400 ppm was investigated using digital spectrophotometry. Polyethylene Glycols 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 32440119-6 2020 The staining effect on dentin and enamel for the 2.5% NaF solutions with PEG-AgNPs at 12,800, 6400, 1600, and 400 ppm was investigated using digital spectrophotometry. agnps 77-82 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 32440119-8 2020 Results: The PEG-AgNPs have an average diameter of 2.56+-0.43 nm and showed excellent stability at high ionic strength (2.5% NaF) for 18 months. Polyethylene Glycols 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 32440119-12 2020 Conclusion: A biocompatible solution of NaF with PEG-AgNPs was developed. peg-agnps 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 32366417-9 2020 CONCLUSION: The paracrine interaction between BCa cells and TAMs led to enhanced BCa cell growth, migration, and invasiveness, and moreover, increased IL-8 and CCL5 cytokine production in tumor microenvironment. Tamoxifen 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 32431615-0 2020 Free Fatty Acid Receptor 1 Signaling Contributes to Migration, MMP-9 Activity, and Expression of IL-8 Induced by Linoleic Acid in HaCaT Cells. Fatty Acids, Nonesterified 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 32431615-0 2020 Free Fatty Acid Receptor 1 Signaling Contributes to Migration, MMP-9 Activity, and Expression of IL-8 Induced by Linoleic Acid in HaCaT Cells. Linoleic Acid 113-126 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 32431615-8 2020 Besides, HaCaT cells stimulated with LA or GW9508 increased the activity of MMP-9 and the expression of IL-8. GW9508 43-49 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 32431615-12 2020 Furthermore, IL-8 secreted by HaCaT cells stimulated with LA or GW9508, contributed to neutrophil chemotaxis. GW9508 64-70 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 32200535-4 2020 By inhibition of NF-kappaB, 1,8-cineole, at relevant plasma concentrations (1.5 microg/ml), strongly and significantly inhibited in normal human monocyte lipopolysaccharide (LPS)-stimulated cytokines relevant for exacerbation (tumour necrosis factor alpha (TNFalpha), interleukin (IL)-1beta and systemic inflammation (IL-6, IL-8). Eucalyptol 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 324-328 32312819-4 2020 To explore this issue, we analyzed secretomes from glucose-deprived cells, which revealed up-regulation of multiple cytokines and chemokines, including IL-6 and IL-8, in response to starvation stress. Glucose 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 32312819-7 2020 Furthermore, glutamine deprivation, as well as the antimetabolic drugs 2-deoxyglucose and metformin, also promoted the release of IL-6 and IL-8. Glutamine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 32312819-7 2020 Furthermore, glutamine deprivation, as well as the antimetabolic drugs 2-deoxyglucose and metformin, also promoted the release of IL-6 and IL-8. Deoxyglucose 71-85 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 32312819-7 2020 Furthermore, glutamine deprivation, as well as the antimetabolic drugs 2-deoxyglucose and metformin, also promoted the release of IL-6 and IL-8. Metformin 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 31935110-7 2020 The metabolites produced by our consortium increased glycogen synthesis by ~57% and decreased proinflammatory markers such as IL-8 by 12%, thus elucidating the positive effect of our consortium on metabolic function and low-grade inflammation. Glycogen 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 32275470-7 2020 Additionally, the upregulated expression of inflammatory cytokines, IL-6 and IL-8, after histamine stimulation was abolished by silencing Orai1 or STIM1 with RNAi in LECs. Histamine 89-98 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 28861755-0 2020 Clarithromycin decreases rhinovirus replication and cytokine production in nasal epithelial cells from subjects with bronchial asthma: effects on IL-6, IL-8 and IL-33. Clarithromycin 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 32088265-4 2020 Chloroquine and hydroxychloroquine increased IL-1beta-induced CXCL8 secretion in macrophages which was critically dependent on the lysosomotropic character and inhibition of macroautophagy but independent from the NLRP3 inflammasome. Chloroquine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 32058018-12 2020 RESULTS: There was a statistically significant correlation between fluoride activity in the 18F-NaF PET scan and histomorphometric parameters such as bone formation rate, activation frequency and osteoclast and osteoblast surfaces and mineralized surfaces. Fluorides 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 32088265-4 2020 Chloroquine and hydroxychloroquine increased IL-1beta-induced CXCL8 secretion in macrophages which was critically dependent on the lysosomotropic character and inhibition of macroautophagy but independent from the NLRP3 inflammasome. Hydroxychloroquine 16-34 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 32058018-15 2020 CONCLUSIONS: A clear correlation between histomorphometric parameters and fluoride activity in the 18F-NaF PET scan was established. Fluorides 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 32205228-10 2020 Cadmium exposures were associated with increased IL-1beta (beta = 77.8 +- 26.3, p = 0.003) and IL-8 (beta = 419.5 +- 201.2, p = 0.04). Cadmium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 31677006-10 2020 Plasma levels of IL-1beta, IL-6 and IL-8 were significantly repressed by geniposide treatment in TBI rats, whereas IL-10 level was upregulated. geniposide 73-83 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 31943712-5 2020 The results showed that nickel could induce cell apoptosis, increase oxidative stress, and promote the expression of pro-inflammatory cytokines, including tumor necrosis factor-alpha, interleukin (IL)-1beta, IL-6, IL-8, C-reaction protein. Nickel 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 33073254-7 2020 As expected, DEX treatment suppressed multiple LPS-induced pro-inflammatory cytokines (IFN-gamma, IL-6, IL-8, IL-1beta, .TNF-alpha) by >85% and increased the anti-inflammatory cytokine IL-10 by 80%. Dexamethasone 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 32277559-9 2020 In addition, incubation of PMN with N-Gel effectively reduced both TNF-alpha and IL-8 mRNA levels. Nitrogen 29-30 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 32269608-6 2020 IC50-Dex was determined through observation of Dex inhibition of tumor necrosis factor-alpha (TNF-alpha)-induced interleukin (IL)-8 release. Dexamethasone 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 113-131 32269608-6 2020 IC50-Dex was determined through observation of Dex inhibition of tumor necrosis factor-alpha (TNF-alpha)-induced interleukin (IL)-8 release. Dexamethasone 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 113-131 32269608-8 2020 Theophylline and Dex pre-treatment was shown to significantly reduce the CSE-induced release of IL-8 and TNF-alpha. Theophylline 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 32269608-8 2020 Theophylline and Dex pre-treatment was shown to significantly reduce the CSE-induced release of IL-8 and TNF-alpha. Dexamethasone 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 32205228-12 2020 Among obese participants (n = 108), benzene, lead, and cadmium were each positively associated with CK18 M30, IL-1beta, IL-6, and IL-8. Benzene 36-43 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 32205228-12 2020 Among obese participants (n = 108), benzene, lead, and cadmium were each positively associated with CK18 M30, IL-1beta, IL-6, and IL-8. Cadmium 55-62 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 31760503-2 2020 BT may be identified and characterized using 18-F-sodium fluoride-positron-emission-tomography/computed tomography (18F-NaF-PET/CT). 18-f-sodium fluoride 45-65 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 32045605-14 2020 Slp2 and LC2029 inhibited Il-8 production in Caco-2 and HT-29 cells induced by MALP-2 and increased production of anti-inflammatory cytokine Il-6. macrophage stimulatory lipopeptide 2 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 32141631-5 2020 The HC with high levels of IgA-ACPA (n = 27) also had significantly higher levels of total IgG, total IgA, and IL-8 in the GCF than the HC with low levels of IgA-ACPA in the GCF (n = 124). 3-[3-[3-[(4~{s})-6-Azanyl-5-Cyano-3-Methyl-4-Propan-2-Yl-2~{h}-Pyrano[2,3-C]pyrazol-4-Yl]-5-(Trifluoromethyl)phenyl]phenyl]propanoic Acid 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 32142400-11 2020 Among the reviewed self-applied topical fluoride methods, daily use of a 0.2% sodium fluoride (NaF) mouth rinse is most likely to be the most effective, followed by 1100 ppm to 1500 ppm fluoride toothpaste plus 0.05% NaF mouth rinse, and 1100 ppm to 1500 ppm fluoride toothpaste. Fluorides 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 32142400-11 2020 Among the reviewed self-applied topical fluoride methods, daily use of a 0.2% sodium fluoride (NaF) mouth rinse is most likely to be the most effective, followed by 1100 ppm to 1500 ppm fluoride toothpaste plus 0.05% NaF mouth rinse, and 1100 ppm to 1500 ppm fluoride toothpaste. Sodium Fluoride 78-93 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 32142400-11 2020 Among the reviewed self-applied topical fluoride methods, daily use of a 0.2% sodium fluoride (NaF) mouth rinse is most likely to be the most effective, followed by 1100 ppm to 1500 ppm fluoride toothpaste plus 0.05% NaF mouth rinse, and 1100 ppm to 1500 ppm fluoride toothpaste. Fluorides 85-93 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 32142400-11 2020 Among the reviewed self-applied topical fluoride methods, daily use of a 0.2% sodium fluoride (NaF) mouth rinse is most likely to be the most effective, followed by 1100 ppm to 1500 ppm fluoride toothpaste plus 0.05% NaF mouth rinse, and 1100 ppm to 1500 ppm fluoride toothpaste. Fluorides 85-93 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 32171180-8 2020 Stimulation of hpGCs with DHT resulted in downregulation of PEDF mRNA expression, concomitantly with a significant increase in IL-6 and IL-8 mRNAs expression. Dihydrotestosterone 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 31896762-7 2020 DMPA-cytokine associations frequently differed by vaginal microbiome; in non-Lactobacillus-dominant women, DMPA was associated with elevated IL-8, MCP-1, and IP-10 concentrations. N,N-dimethyl-4-anisidine 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 32029577-10 2020 Cin significantly inhibited IL-1beta-induced interleukin-6 (IL-6), interleukin-8 (IL-8), and tumor necrosis factor-alpha (TNF-alpha) release from human synoviocyte cells. cinnamaldehyde 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 32029577-10 2020 Cin significantly inhibited IL-1beta-induced interleukin-6 (IL-6), interleukin-8 (IL-8), and tumor necrosis factor-alpha (TNF-alpha) release from human synoviocyte cells. cinnamaldehyde 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 31896762-7 2020 DMPA-cytokine associations frequently differed by vaginal microbiome; in non-Lactobacillus-dominant women, DMPA was associated with elevated IL-8, MCP-1, and IP-10 concentrations. N,N-dimethyl-4-anisidine 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 32370100-8 2020 Cell cycle analysis demonstrated that K562 cells treated with Br-Ell-SO3Na were arrested in the phase S. Moreover, the production of IL-6 increased and the expression of IL-8 was inhibited in the human PBMC treated with Br-Ell-SO3Na. br-ell-so3na 62-74 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 32370100-8 2020 Cell cycle analysis demonstrated that K562 cells treated with Br-Ell-SO3Na were arrested in the phase S. Moreover, the production of IL-6 increased and the expression of IL-8 was inhibited in the human PBMC treated with Br-Ell-SO3Na. br-ell-so3na 220-232 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 32405062-2 2020 Here, using a large-scale retrospective analysis, we show that elevated baseline serum IL-8 levels are associated with poor outcome in patients (n = 1,344) with advanced cancers treated with nivolumab and/or ipilimumab, everolimus or docetaxel in phase 3 clinical trials, revealing the importance of assessing serum IL-8 levels in identifying unfavorable tumor immunobiology and as an independent biomarker in patients receiving immune-checkpoint inhibitors. Everolimus 220-230 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 32405062-2 2020 Here, using a large-scale retrospective analysis, we show that elevated baseline serum IL-8 levels are associated with poor outcome in patients (n = 1,344) with advanced cancers treated with nivolumab and/or ipilimumab, everolimus or docetaxel in phase 3 clinical trials, revealing the importance of assessing serum IL-8 levels in identifying unfavorable tumor immunobiology and as an independent biomarker in patients receiving immune-checkpoint inhibitors. Docetaxel 234-243 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 32126272-3 2020 Owing to its potent antioxidant properties, lycopene can potentially alleviate enhanced levels of proinflammatory mediators (e.g., proinflammatory cytokines IL-8, -6, and -1, and oxidized phospholipids) and prevent NF-kappaB activation by modulating oxidative stress. Lycopene 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 157-173 32326355-7 2020 Both trichothecenes also enhanced transcript levels of the known NF-kappaB-dependent pro-inflammatory cytokines IL-8, IL-6, TNF-alpha and IL-1beta. Trichothecenes 5-19 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 32186753-9 2020 Further mechanistic studies indicated that resveratrol exerted anti-inflammatory activity by activating the ERK1/2 pathway, decreasing the secretion of interleukin (IL)-6 and IL-8 induced by TNF-alpha, and enhancing hPDLSCs osteogenesis. Resveratrol 43-54 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 32354131-6 2020 The DOX-stimulated expression of IkappaBalpha, NF-kappaB, COX-2, and IL-8 were all downregulated by exercise as well as the fibrosis factors (TGF-beta1, phosphorylated ERK, Sp1, and CTGF). Doxorubicin 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 32368057-1 2020 Objective: To investigate the remineralizing and staining effects of sodium fluoride (NaF) solution with polyethylene glycol-coated silver nanoparticles (PEG-AgNPs) on artificial dentine caries. Sodium Fluoride 69-84 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 32368057-1 2020 Objective: To investigate the remineralizing and staining effects of sodium fluoride (NaF) solution with polyethylene glycol-coated silver nanoparticles (PEG-AgNPs) on artificial dentine caries. Polyethylene Glycols 105-124 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 32368057-1 2020 Objective: To investigate the remineralizing and staining effects of sodium fluoride (NaF) solution with polyethylene glycol-coated silver nanoparticles (PEG-AgNPs) on artificial dentine caries. Silver 132-152 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 32368057-14 2020 Conclusion: The use of NaF solution with PEG-AgNPs can remineralize artificial dentine caries and inhibit collagen degradation without causing significant tooth staining. Polyethylene Glycols 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 32368057-14 2020 Conclusion: The use of NaF solution with PEG-AgNPs can remineralize artificial dentine caries and inhibit collagen degradation without causing significant tooth staining. agnps 45-50 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 32365773-0 2020 Sildenafil Reduces Expression and Release of IL-6 and IL-8 Induced by Reactive Oxygen Species in Systemic Sclerosis Fibroblasts. Sildenafil Citrate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 32365773-5 2020 Treatment with sildenafil significantly reduced dermal fibroblast gene expression and cellular release of IL-6, known to play a central role in the pathogenesis of tissue damage in SSc and IL-8, directly induced by ROS. Sildenafil Citrate 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 32365773-5 2020 Treatment with sildenafil significantly reduced dermal fibroblast gene expression and cellular release of IL-6, known to play a central role in the pathogenesis of tissue damage in SSc and IL-8, directly induced by ROS. Reactive Oxygen Species 215-218 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 32598720-9 2020 68% of patients with exacerbation of CP, receiving in addition to the standard regimen rifaximin, achieved clinical improvement, normalization of intestinal biocenosis, reduced concentrations of cytokines in tissues, reducing signs of chronic inflammation in the colon mucosa with reducing concentrations of IL-2, IL-6, IL-8 in colon mucosa (p0.05). Rifaximin 87-96 C-X-C motif chemokine ligand 8 Homo sapiens 320-324 32322697-1 2020 Objectives: To evaluate effectiveness of a nasal resveratrol/carboxymethyl-beta-glucan solution compared to nasal saline solution: a) on common cold symptoms by means of a validated measure scale (CARIFS score), b) on Rhinovirus infection and CCL2, CCL5, IL8, IL6, CXCL10 and TLR2 expression in nasal swabs, c) on frequency of relapses after 30 days of follow-up. Resveratrol 49-60 C-X-C motif chemokine ligand 8 Homo sapiens 255-258 32315368-2 2020 The platelet, one of the main activators of neutrophils, contains Interleukin 8 (IL-8), a potent neutrophil chemo-attractant and P-selectin that induces excretion of superoxide in the neutrophils, forming platelet-neutrophil aggregates that are increased in individuals with active UC, hence an index of both cells could produce a monitoring tool. Superoxides 166-176 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 32315368-2 2020 The platelet, one of the main activators of neutrophils, contains Interleukin 8 (IL-8), a potent neutrophil chemo-attractant and P-selectin that induces excretion of superoxide in the neutrophils, forming platelet-neutrophil aggregates that are increased in individuals with active UC, hence an index of both cells could produce a monitoring tool. Superoxides 166-176 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 32316988-5 2020 RESULTS: Exposure to both Si10 and Min-U-Sil induced gene expression and release of CXCL8, interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-alpha), interleukin-1alpha (IL-1alpha) and interleukin-1beta (IL-1beta) in a concentration-dependent manner. si10 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 84-89 33611501-4 2020 METHODS AND RESULTS: After a structured PubMed search, we identified 18F-sodium fluoride (18F-NaF) PET as the most suitable technique for detecting micro-calcification. 18f-sodium fluoride 69-88 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 32022261-7 2020 RESULTS: Treatment with APG-157 resulted in circulating concentrations of curcumin and analogs peaking at 3 hours with reduced IL-1beta, IL-6, and IL-8 concentrations in the salivary supernatant fluid of patients with cancer. apg 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 32316237-1 2020 This study measures the total graft of 18F-sodium fluoride (NaF) uptake in non-instrumented posterolateral lumbar fusion (niPLF) patients one month after surgery and correlates it with the difference in the clinical findings between the baseline and one year after surgery. 18f-sodium fluoride 39-58 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 32015100-3 2020 In the present report, we present clear evidence that these senescence-related active fibroblasts can dedifferentiate proliferating primary human luminal cells to multipotent stem cells in an interleukin-8 (IL-8)-dependent manner. Phenobarbital 146-153 C-X-C motif chemokine ligand 8 Homo sapiens 192-205 32419980-1 2020 The goal of this study was to assess pulmonary artery calcification in healthy controls and subjects with suspicion of stable angina pectoris through the usage of quantitative 18F-sodium fluoride positron emission tomography/computed tomography (NaF-PET/CT). 18f-sodium fluoride 176-195 C-X-C motif chemokine ligand 8 Homo sapiens 246-249 32419980-8 2020 For global SUVmean (0.79 compared to 0.58), global TBRmean (1.15 compared to 0.93), and global SUVmax (1.78 compared to 1.60), the NaF uptake was significantly higher in the at-risk patients compared to the controls (all P<0.05). tbrmean 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 32326546-6 2020 Among patients with CF, IL-6 and IL-8 were significantly higher in patients with NTH, while TNF-alpha was significantly lower in patients with NP. SUCCINIC ACID MONO-(13-METHYL-3-OXO-2,3,6,7,8,9,10,11,12,13,14,15,16,17-TETRADECAHYDRO-1H-CYCLOPENTA[A]PHENANTHREN-17-YL) ESTER 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 32015100-3 2020 In the present report, we present clear evidence that these senescence-related active fibroblasts can dedifferentiate proliferating primary human luminal cells to multipotent stem cells in an interleukin-8 (IL-8)-dependent manner. Phenobarbital 146-153 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 32015100-5 2020 This IL-8-related dedifferentiation of luminal cells was mediated through the STAT3-dependent downregulation of p16INK4A and the microRNA miR-141. Phenobarbital 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 31525453-9 2020 CONCLUSION: Infection of cervicovaginal epithelial cells by U. urealyticum stimulates production of ammonia from urea and induces elevated IL-8 production possibly leading to significantly higher cytotoxicity. Urea 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 32271889-13 2020 Cis-UCA decreased the release of IL-6, IL-8, and LDH in a time-dependent manner when administered to HCE-2 cells after UV-B exposure. cis-Urocanic acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 32271889-15 2020 Cis-UCA can prevent the secretion of IL-1beta and IL-18 and therapeutically reduces the levels of IL-6, IL-8, and LDH in UV-B-stressed HCE cells. cis-Urocanic acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 32055907-3 2020 In principle, target IL-8 is first treated with the reducing agent tris(2-carboxyethyl)phosphine (TCEP) to yield active thiols and then captured by antibody-functionalized magnetic beads (MBs). tris(2-carboxyethyl)phosphine 67-96 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 32150447-3 2020 We found that a single treatment with 50 microM cisplatin induces hepatitis A virus cellular receptor 1 (HAVCR1) and C-X-C motif chemokine ligand 8 (CXCL8) expression, DNA damage (gammaH2AX), and cell death in the organoids but greatly impairs organoid viability. Cisplatin 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 117-147 32150447-3 2020 We found that a single treatment with 50 microM cisplatin induces hepatitis A virus cellular receptor 1 (HAVCR1) and C-X-C motif chemokine ligand 8 (CXCL8) expression, DNA damage (gammaH2AX), and cell death in the organoids but greatly impairs organoid viability. Cisplatin 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 149-154 32055907-3 2020 In principle, target IL-8 is first treated with the reducing agent tris(2-carboxyethyl)phosphine (TCEP) to yield active thiols and then captured by antibody-functionalized magnetic beads (MBs). tris(2-carboxyethyl)phosphine 98-102 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 32055907-3 2020 In principle, target IL-8 is first treated with the reducing agent tris(2-carboxyethyl)phosphine (TCEP) to yield active thiols and then captured by antibody-functionalized magnetic beads (MBs). Sulfhydryl Compounds 120-126 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 32070866-7 2020 Palmitate also induced apoptosis and mRNA expression of IL-6 and IL-8 in the PDLSCs. Palmitates 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 29948889-1 2020 We investigated the impact of reconstruction parameters and cardiac motion-correction in 18F Sodium Fluoride (18F-NaF) PET. Sodium Fluoride 93-108 C-X-C motif chemokine ligand 8 Homo sapiens 114-117 31270902-1 2020 The aim of this study was to assess the influence of ketorolac tromethamine and dexamethasone on substance P and IL-8 expression when used as a root canal irrigant for single visit root canal treatment for acute irreversible pulpitis. Ketorolac Tromethamine 53-75 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 31270902-1 2020 The aim of this study was to assess the influence of ketorolac tromethamine and dexamethasone on substance P and IL-8 expression when used as a root canal irrigant for single visit root canal treatment for acute irreversible pulpitis. Dexamethasone 80-93 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 31270902-8 2020 The sodium hypochlorite group had a higher mean expression of substance P and IL-8 values. Sodium Hypochlorite 4-23 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 31479623-6 2020 Chromosome conformation capture (3C) analysis demonstrated the strengthening or loss of specific long-range chromatin interactions in response to rapamycin and quiescence induction, including a cluster of genes containing Interleukin-8 and several chemokine genes on chromosome 4. Sirolimus 146-155 C-X-C motif chemokine ligand 8 Homo sapiens 222-235 32047095-6 2020 We also found suggestive cross-associated loci for neonatal and maternal vitamin D near immune genes, such as CXCL6-IL8 and ACKR1 We found no interactions with ASD. Vitamin D 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 32041439-10 2020 Sulforaphane significantly inhibited the levels of inflammatory mediators including TSLP, tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, IL-6, and IL-8 in a dose-dependent manner. sulforaphane 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 31773440-6 2020 Results disclosed that ar-turmerone dose-dependently suppressed proliferation, facilitated apoptosis, and reduced TNF-alpha-mediated production of interleukin (IL)-1beta, IL-6, and IL-8 in HaCaT cells. ar-turmerone 23-35 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 31974519-4 2020 The production of interleukin (IL)-6 and IL-8 by human epidermal keratinocytes stimulated by heat-killed Cutibacterium acnes was significantly inhibited by ozenoxacin at concentrations from 1 to 30 mug ml-1. ozenoxacin 156-166 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 31974519-5 2020 Likewise, the production of IL-6, IL-8, and tumor necrosis factor alpha by stimulated THP-1 cells, a human monocyte cell line, was inhibited by ozenoxacin at concentrations from 1 to 30 mug ml-1. ozenoxacin 144-154 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 31950542-3 2020 Pre-exposure of 1.5% isoflurane for 0.5 h induced anti-inflammatory effects (measured by cytokine production of TNF-alpha, IL-8, and IL-1beta) in both human THP-1 cells and primary human peripheral blood monocytes stimulated by lipopolysaccharide. Isoflurane 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 31691303-11 2020 CONCLUSIONS: NaF and NaOCl solutions were able to electrochemically dissolve PTU F1 and WOGS instruments. Propylthiouracil 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 31782556-5 2020 The dextran sulfate plasma adsorption system reduced IFN-gamma, IL-8, IL-1ra, eotaxin, TNF, MCP-1, PDGF-BB, MIP-1beta, and IP-10 (P < .05). Sulfates 12-19 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 31935586-2 2020 Ag nanoparticles were employed in freestanding and binder-free F-GNS electrode (the composite film electrode was labeled as FGA) as catalyst, which were shown to strongly facilitate the decomposition of NaF during charge process in sodium/carbon fluorides (Na/CFx) secondary batteries. Sodium 232-238 C-X-C motif chemokine ligand 8 Homo sapiens 203-206 31935586-2 2020 Ag nanoparticles were employed in freestanding and binder-free F-GNS electrode (the composite film electrode was labeled as FGA) as catalyst, which were shown to strongly facilitate the decomposition of NaF during charge process in sodium/carbon fluorides (Na/CFx) secondary batteries. Carbon 239-255 C-X-C motif chemokine ligand 8 Homo sapiens 203-206 31202739-8 2020 The predictive value of both 18F-FDG (cut-off TBRmax value of 1.98) and 18F-NaF (cut-off TBRmax value of 2.11) uptake demonstrated excellent discrimination in predicting 1-year restenosis (Kaplan Meier estimator, log-rank p < 0.001). tbrmax 89-95 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 32885098-7 2020 Both 15% Ag-SiO2 and CuO exposure produced significantly higher levels of IL-8 in the co-culture compared with A549 cells alone. Silicon Dioxide 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 30961342-11 2020 After conventional therapy, levels of IL-6 (P=0.001) and IL-8 (P=0.001) significantly decreased in caffeine citrate prevention group compared with those in caffeine citrate treatment group. caffeine citrate 99-115 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 32308752-9 2020 Results: Both in vivo and in vitro experiments showed that sodium fluoride (NaF) caused mitochondrial dysfunction and impaired mitochondrial biogenesis. Sodium Fluoride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 31954196-6 2020 Furthermore, the levels of IL-6 and IL-8 showed a stronger correlation with corneal fluorescein staining (CFS) (P<0.05), and the levels of IL-6 and ICAM-1 were most consistent with fluorescein tear film break-up time (TBUT) (P<0.05). Fluorescein 84-95 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 31893611-0 2020 Methyl linderone suppresses TPA-stimulated IL-8 and MMP-9 expression via the ERK/STAT3 pathway in MCF-7 breast cancer cells. linderone A 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 31893611-0 2020 Methyl linderone suppresses TPA-stimulated IL-8 and MMP-9 expression via the ERK/STAT3 pathway in MCF-7 breast cancer cells. Tetradecanoylphorbol Acetate 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 31893611-6 2020 Moreover, it inhibited two metastasis-related factors, matrix metalloproteinase-9 (MMP-9) and interleukin-8 (IL-8), at the mRNA and protein expression levels, in TPA-treated MCF-7 cells. Tetradecanoylphorbol Acetate 162-165 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 31893611-6 2020 Moreover, it inhibited two metastasis-related factors, matrix metalloproteinase-9 (MMP-9) and interleukin-8 (IL-8), at the mRNA and protein expression levels, in TPA-treated MCF-7 cells. Tetradecanoylphorbol Acetate 162-165 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 32292492-7 2020 Methylprednisolone group, compared to Cytosorb and Control had significantly lower levels of TNF-alpha (until the end of surgery, p < 0.001), IL-6 (until 48 h after surgery, p < 0.001), and IL-8 (until 24 h after surgery, p < 0.016). Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 32218354-5 2020 Vildagliptin is able to limit inflammation by suppression of the NF-kappaB (nuclear factor kappa-light-chain-enhancer of activated B cells) signaling pathway and proinflammatory agents such as TNF-alpha (tumor necrosis factor alpha), IL-1beta (Interleukin-1beta), and IL-8 (Interleukin 8). Vildagliptin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 268-272 32218354-5 2020 Vildagliptin is able to limit inflammation by suppression of the NF-kappaB (nuclear factor kappa-light-chain-enhancer of activated B cells) signaling pathway and proinflammatory agents such as TNF-alpha (tumor necrosis factor alpha), IL-1beta (Interleukin-1beta), and IL-8 (Interleukin 8). Vildagliptin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 274-287 32183324-1 2020 The anodic polarization response of magnesium alloy AZ31 was first characterized during exposure to aerated 0.1 M NaCl solutions with millimolar additions of NaVO3, Na3PO4, Na2HPO4, NaF and various pairings to assess their ability to inhibit corrosion kinetics and retard localized corrosion. Magnesium 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 32197426-0 2020 Identification of Interleukin-8-Reducing Lead Compounds Based on SAR Studies on Dihydrochalcone-Related Compounds in Human Gingival Fibroblasts (HGF-1 cells) In Vitro. dihydrochalcone 80-95 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 32256360-9 2020 The in vitro anti-inflammatory activity was carried out on monosodium urate (MSU) crystal-induced pro-inflammatory cytokines (i.e., interleukin (IL)1alpha, IL-1beta, IL-6, IL-8, and tumor necrosis factor (TNF)-alpha) secretion using human peripheral blood mononuclear cells and ELISA technique, and prostaglandin E2 (PGE2)secretion using radioimmunoassay. Uric Acid 59-75 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 32256360-9 2020 The in vitro anti-inflammatory activity was carried out on monosodium urate (MSU) crystal-induced pro-inflammatory cytokines (i.e., interleukin (IL)1alpha, IL-1beta, IL-6, IL-8, and tumor necrosis factor (TNF)-alpha) secretion using human peripheral blood mononuclear cells and ELISA technique, and prostaglandin E2 (PGE2)secretion using radioimmunoassay. Uric Acid 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 32185685-7 2021 Higher CT calcium mass, total cholesterol, and HbA1c were associated with higher 18F-NaF TBR after adjusting. Calcium 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 32185685-8 2021 CONCLUSION: This study shows that several modifiable cardiovascular risk factors (total cholesterol, triglycerides, HbA1c) are associated with femoral 18F-NaF tracer uptake in patients with type 2 diabetes. Cholesterol 88-99 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 32185685-8 2021 CONCLUSION: This study shows that several modifiable cardiovascular risk factors (total cholesterol, triglycerides, HbA1c) are associated with femoral 18F-NaF tracer uptake in patients with type 2 diabetes. Triglycerides 101-114 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 32192002-4 2020 According to our knowledge, the present study is the first to evaluate the clinical usefulness of serum CXCL-8 (C-X-C motif chemokine 8) in the diagnosis and progression of CRC compared to classical tumor marker CEA (carcinoembryonic antigen) and marker of inflammation CRP (C-reactive protein). c-x-c 112-117 C-X-C motif chemokine ligand 8 Homo sapiens 104-110 32226841-4 2020 The results indicated that Na2UF8 on the NaF sorbent was stable under 300 C in the argon atmosphere, and it started to decompose into UF6 and NaF rapidly when the temperature was above 300 C. Meanwhile, a small amount of Na2UF8 was converted to Na3UF7, and it was stable in the temperature range from 350 to 450 C. The decomposition mechanism of the Na2UF8 and the formation mechanism of Na3UF7 on the NaF sorbent were speculated according to the experimental results. na2uf8 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 32226841-4 2020 The results indicated that Na2UF8 on the NaF sorbent was stable under 300 C in the argon atmosphere, and it started to decompose into UF6 and NaF rapidly when the temperature was above 300 C. Meanwhile, a small amount of Na2UF8 was converted to Na3UF7, and it was stable in the temperature range from 350 to 450 C. The decomposition mechanism of the Na2UF8 and the formation mechanism of Na3UF7 on the NaF sorbent were speculated according to the experimental results. na2uf8 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 143-146 32226841-4 2020 The results indicated that Na2UF8 on the NaF sorbent was stable under 300 C in the argon atmosphere, and it started to decompose into UF6 and NaF rapidly when the temperature was above 300 C. Meanwhile, a small amount of Na2UF8 was converted to Na3UF7, and it was stable in the temperature range from 350 to 450 C. The decomposition mechanism of the Na2UF8 and the formation mechanism of Na3UF7 on the NaF sorbent were speculated according to the experimental results. na2uf8 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 143-146 32226841-4 2020 The results indicated that Na2UF8 on the NaF sorbent was stable under 300 C in the argon atmosphere, and it started to decompose into UF6 and NaF rapidly when the temperature was above 300 C. Meanwhile, a small amount of Na2UF8 was converted to Na3UF7, and it was stable in the temperature range from 350 to 450 C. The decomposition mechanism of the Na2UF8 and the formation mechanism of Na3UF7 on the NaF sorbent were speculated according to the experimental results. Argon 84-89 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 32256360-16 2020 In vitro anti-inflammatory assay showed that extract of MPP roots inhibited MSU crystals-induced secretion of IL-1alpha, IL-1beta, IL-8, TNF-alpha, and PGE2 with IC50 values of 36, 25, 38, 18, and 46 mug/mL, respectively. Uric Acid 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 32196098-6 2020 Results: Treatment with noncytotoxic concentrations of GS resulted in the dose-dependent inhibition of IL-1beta-induced inflammatory cytokines, including IL-6, IL-8, MCP-1, and COX-2, at both mRNA and protein levels. pregna-4,17-diene-3,16-dione 55-57 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 32218789-13 2020 IC87114 decreased poly I:C-induced PD-L1 expression on PBECs and secretion of IL-6 and IL-8 into culture supernatants. Poly I 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 32218789-13 2020 IC87114 decreased poly I:C-induced PD-L1 expression on PBECs and secretion of IL-6 and IL-8 into culture supernatants. Carbon 1-2 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 32064872-4 2020 In porcine intestinal epithelial cells (IPEC-J2), L-arginine obviously suppressed (p < 0.05) the levels of IL-6 (220.63 +- 2.82), IL-8 (333.95 +- 3.75), IL-1beta (693.08 +- 2.38) and TNF-alpha (258.04 +- 4.14) induced by LPS. Arginine 50-60 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 32150886-7 2020 The release of IL-1beta, IL-8, MCP-1 and M-CSF proteins was mainly affected in macrophages after metal ion exposure (100 microM), indicating a higher impact on pro-inflammatory activity. Metals 97-102 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 32210955-8 2020 Concentrations of VCAM-1, intercellular adhesion molecule-1 (ICAM-1), and IL-8 strongly correlated with total heme levels in CSF. Heme 110-114 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 32139669-4 2020 In vitro, both knockdown of TRPC6 expression with shRNA and TRPC6 blockage markedly attenuated the release of cytokines IL-6 and IL-8 induced by O3 or H2O2 in 16HBE cells (human bronchial epithelial cell line). Ozone 145-147 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 32139669-4 2020 In vitro, both knockdown of TRPC6 expression with shRNA and TRPC6 blockage markedly attenuated the release of cytokines IL-6 and IL-8 induced by O3 or H2O2 in 16HBE cells (human bronchial epithelial cell line). Hydrogen Peroxide 151-155 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 32139808-0 2021 Hippocampal TNF-death receptors, caspase cell death cascades, and IL-8 in alcohol use disorder. Alcohols 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 32065293-9 2020 Notably, DON-induced interleukin-8 transcription and secretion were diminished by the presence of 10 and 25 ng/mL CER after short-term (5 h) incubation, indicating immunosuppressive properties. deoxynivalenol 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 32135490-8 2020 Pristimerin dramatically inhibited the expression of TNF-alpha-induced endothelial adhesion molecules (intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1)) and the pro-inflammatory cytokine (IL-6, IL-8 and monocyte chemoattractant protein-1 (MCP-1)). pristimerin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 31486595-8 2020 RESULTS: Tear levels of IL-8 were significantly increased in patients with oMMP (260.1 +- 70 pg/ml) when compared to both HCs (98.5 +- 71.35 pg/ml; p = 0.001) and patients with pSS (96.3 +- 87.5 pg/ml; p = 0.001). ommp 75-79 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 31486595-8 2020 RESULTS: Tear levels of IL-8 were significantly increased in patients with oMMP (260.1 +- 70 pg/ml) when compared to both HCs (98.5 +- 71.35 pg/ml; p = 0.001) and patients with pSS (96.3 +- 87.5 pg/ml; p = 0.001). pss 177-180 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 32065293-9 2020 Notably, DON-induced interleukin-8 transcription and secretion were diminished by the presence of 10 and 25 ng/mL CER after short-term (5 h) incubation, indicating immunosuppressive properties. cereulide 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 31927406-8 2020 SBU supernatant increased the frequency of monocytes expressing IL-8 and decreased the monocytes expressing IL-10. sbu 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 31927406-9 2020 Considering S. mutans-stimulated cells, while SBU increased the frequency of IL-8+ monocytes, CSEB reduced the frequency of IL-6 and TNF-alpha positive monocytes. sbu 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 31962250-4 2020 BmV at 50 and 75 microg/mL reduced CXCL8/IL-8 (p < 0.001 and p < 0.01, respectively) and CCL2/MCP-1 production (p < 0.05), while BmooLAAO-I at the same concentrations reduced only CCL2/MCP-1 production (p < 0.01). 7-cyano-2,3,4,5-tetrahydro-1-(1H-imidazol-4-ylmethyl)-3-(phenylmethyl)-4-(2-thienylsulfonyl)-1H-1,4-benzodiazepine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 32113050-1 2020 BACKGROUND AND AIMS: Molecular imaging with 18Fluorodeoxyglucose (FDG) and 18F-sodium-fluoride (NaF) captures arterial inflammation and micro-calcification and can reveal potentially unstable atherosclerotic plaques. 18f-sodium-fluoride 75-94 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 31327083-8 2020 DOXY group exhibited a significant increase in the levels of anti-inflammatory interleukin (IL)-10 and a reduction in IL-8, IFN-y, IL-6, and IL-17 (p < 0.05), significant reduction in periodontal pathogens (p < 0.05), and a lower mean percentage of HbA1C at 3 months (p < 0.05). Doxycycline 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 31758423-9 2020 IGU, MTX, and DXM dose dependently decreased the secretion of TNF-alpha, IL-1beta, IL-6, and IL-8 in neutrophils and PBMCs (P < 0.05); the inhibitory effect of IGU was not significantly different from that of MTX and DXM. Methotrexate 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 31758423-9 2020 IGU, MTX, and DXM dose dependently decreased the secretion of TNF-alpha, IL-1beta, IL-6, and IL-8 in neutrophils and PBMCs (P < 0.05); the inhibitory effect of IGU was not significantly different from that of MTX and DXM. Dexamethasone 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 31754794-0 2020 18F-Fluoride (18F-NaF) PET/CT in medullary thyroid carcinoma: far from evidence, far from guidelines! Fluorides 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 31754794-0 2020 18F-Fluoride (18F-NaF) PET/CT in medullary thyroid carcinoma: far from evidence, far from guidelines! CP-18 compound 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 32015511-7 2020 Nintedanib greatly reduced the levels of cancer-promoting cytokines, such as interleukin (IL)-6 (IL-6) and IL-8, secreted by CAFs. nintedanib 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 32556016-8 2020 However, when analyzing the TSL, it was observed that Ca2+-MSNs, TiF4, and NaF were more effective in preventing dental erosion versus CPP-ACP, CPP-ACP/F-, and Milli-Q water (p< 0.05). Water 169-174 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 32164454-3 2020 This study investigates (1) 18F-fluorodeoxyglucose (FDG) and 18F-sodium fluoride (NaF) uptake in culprit versus nonculprit carotid atheroma, (2) spatial distributions of uptake, and (3) how macrocalcification affects this relationship. 18f-sodium fluoride 61-80 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 31972422-5 2020 The following proteins were found to occur in both RA-associated networks and triptolide target networks: CD274, RELA, MCL1, MAPK8, CXCL8, STAT1, STAT3, c-JUN, JNK, c-Fos, NF-kappaB, and TNF-alpha. triptolide 78-88 C-X-C motif chemokine ligand 8 Homo sapiens 132-137 31972422-6 2020 Docking studies suggested that triptolide can fit in the binding pocket of the six top candidate triptolide target proteins (CD274, RELA, MCL1, MAPK8, CXCL8 and STAT1). triptolide 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 151-156 31972422-6 2020 Docking studies suggested that triptolide can fit in the binding pocket of the six top candidate triptolide target proteins (CD274, RELA, MCL1, MAPK8, CXCL8 and STAT1). triptolide 97-107 C-X-C motif chemokine ligand 8 Homo sapiens 151-156 31962250-4 2020 BmV at 50 and 75 microg/mL reduced CXCL8/IL-8 (p < 0.001 and p < 0.01, respectively) and CCL2/MCP-1 production (p < 0.05), while BmooLAAO-I at the same concentrations reduced only CCL2/MCP-1 production (p < 0.01). 7-cyano-2,3,4,5-tetrahydro-1-(1H-imidazol-4-ylmethyl)-3-(phenylmethyl)-4-(2-thienylsulfonyl)-1H-1,4-benzodiazepine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 32274105-8 2020 Also, Sch A downregulated the expression of IL-8 and upregulated the expression of HO-1 mRNA in lung epithelial cells and cell supernatants, and resulted in the downregulation of the protein expression level of phosphorylated nuclear factor-kappaB. schizandrin A 6-11 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 31811067-4 2020 Though 18F-sodium fluoride (18F-NaF) was one of the oldest medical tracers but was replaced by other tracers until recently, owing to its physical properties. Sodium Fluoride 7-26 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 31811067-4 2020 Though 18F-sodium fluoride (18F-NaF) was one of the oldest medical tracers but was replaced by other tracers until recently, owing to its physical properties. CP-18 compound 7-10 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 31811067-5 2020 Continued development of positron emission tomographic (PET) scanners have opened a new era for 18F-NaF and given its higher sensitivity, there have been increasing applications in imaging. CP-18 compound 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 31811067-7 2020 Finally, we compared the accuracy of 18F-NaF PET with other conventional imaging for detection of osseous metastasis. CP-18 compound 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 31899823-16 2020 Patients with a detectable PSA after ADT had elevated levels of IL-6 (P = .049) and IL-8 (P = .013) at PSA progression as compared with those with an undetectable PSA. adt 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 31904489-11 2020 An increase in IL-8 during the 6 weeks of KJD was associated with significantly greater improvement in KOOS4 over 12 months. koos4 103-108 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 31927915-9 2020 Finally, we performed functional secretory analysis of interleukin-8 and tumor necrosis factor alpha from human neutrophils and monocytes, stimulated with various doses of lipopolysaccharide and phorbol 12-myristate 13-acetate-ionomycin, respectively. phorbol 12-myristate 13-acetate-ionomycin 195-236 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 32101144-7 2020 Large agglomerates of 17 nm TiO2 induced stronger responses than small agglomerates for glutathione depletion, IL-8 and IL-1beta increase, and DNA damage in THP-1, while no effect of agglomeration was observed with 117 nm TiO2. titanium dioxide 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 32112175-9 2020 In vitro, the PI3K inhibitors (BZE235 and LY294002) ameliorated GC insensitivity in H2O2/TNFalpha-induced IL-8 release from U937 cells by independently restoring the activity of HDAC2 or inhibiting the activation of transcription factors. bze235 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 32112175-9 2020 In vitro, the PI3K inhibitors (BZE235 and LY294002) ameliorated GC insensitivity in H2O2/TNFalpha-induced IL-8 release from U937 cells by independently restoring the activity of HDAC2 or inhibiting the activation of transcription factors. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 42-50 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 32112175-9 2020 In vitro, the PI3K inhibitors (BZE235 and LY294002) ameliorated GC insensitivity in H2O2/TNFalpha-induced IL-8 release from U937 cells by independently restoring the activity of HDAC2 or inhibiting the activation of transcription factors. Hydrogen Peroxide 84-88 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 32120344-6 2020 Of interest, we observed that 1alpha,25(OH)2D3 inhibits NF-kappaB activation and subsequent synthesis and secretion of IL-6 and IL-8 by promoting VDR and NF-kappaB p65 interaction. 25(oh)2d3 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 32211217-9 2020 A preliminary study has shown that [99m Tc]-labelled IL8 may be a possible candidate for imaging of peripheral OM. Technetium 40-42 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 32211218-4 2020 In this study, we aimed to assess 18F-sodium fluoride (18F-NaF) uptake by the aortic valve on PET/CT scans performed in two age groups; 25-35 and 50-75 years of age. 18f-sodium fluoride 34-53 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 31843963-7 2020 Moreover, IpaJ was efficient in the prevention of NF-kappaB translocation to the nucleus and ultimately interfered with the secretion of the proinflammatory cytokines IL-1beta, IL-6, and IL-8 in infected HeLa cells. ipaj 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 33005593-3 2020 Here, we investigated whether sodium fluoride (NaF) has the ability to induce DNA damage and chromosomal abnormalities in human osteosarcoma cells after 48 and 72 h of exposure. Sodium Fluoride 30-45 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 31912731-2 2020 Chemical bath deposited (CBD) CdS layers of different thickness on NaF PDT (CIGSeNaF) and on NaF+KF PDT (CIGSeNaF+KF) Cu(In,Ga)Se2 absorbers prepared at low temperature (to facilitate the use of flexible, e.g. polyimide, substrates) were studied. Cadmium 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 32057253-3 2020 The levels of cytokine and chemokine were analysed with ELISA and real-time PCR.Results: Astragaloside IV significantly inhibited the levels of CCL5, MCP-1, IL-6 and IL-8. astragaloside A 89-102 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 32104118-9 2020 Multiple linear regression analyses led to the identification of ArI (beta=0.026, P<0.05) and TST (beta=-0.054, P<0.05) as significant positive and negative predictors of the IL-8 level, respectively. BAL-ARI8 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 31863766-5 2020 In this study, we found that rapamycin (an mTOR inhibitor) and p70S6K siRNA diminished thrombin-induced IL-8/CXCL8 release. Sirolimus 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 32075981-9 2020 Celecoxib was responsible for only 5% of the variance in bacterial community composition but celecoxib-exposed microbiota preserved barrier function and decreased concentrations of IL-8 and CXCL16 in a donor-dependent manner in our two models simulating gut inflammatory milieu. celecoxib 93-102 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 32079388-6 2020 Sodium fluoride (NaF) PET/CT is a promising imaging modality in evaluation of skeletal system. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 32296583-12 2020 Subsequently, IL-8 recruited neutrophils which in turn mediated NETs formation via the PI3K/AKT/ROS axis in TINs. ros 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 32296583-12 2020 Subsequently, IL-8 recruited neutrophils which in turn mediated NETs formation via the PI3K/AKT/ROS axis in TINs. tins 108-112 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 32296583-13 2020 Conclusions: Our results suggest that NETs produced by TINs mediate the crosstalk between glioma progression and the tumor microenvironment by regulating the HMGB1/RAGE/IL-8 axis. tins 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 32075287-11 2020 The use of curcumin reduces the subjective perception of the intensity of muscle pain; reduces muscle damage through the decrease of creatine kinase (CK); increases muscle performance; has an anti-inflammatory effect by modulating the pro-inflammatory cytokines, such as TNF-alpha, IL-6, and IL-8; and may have a slight antioxidant effect. Curcumin 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 292-296 32117213-6 2019 The relative expression and secretion of IL-6, IL-8, and TNF-alpha in lipopolysaccharide-stimulated microglia were up-regulated in the GSC supernatant group, which could be reversed by dimethyl amiloride (DMA) (EV secretion inhibitor) co-administration or si-MALAT1 pre-transfection of GSCs. 5-dimethylamiloride 185-203 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 32117213-6 2019 The relative expression and secretion of IL-6, IL-8, and TNF-alpha in lipopolysaccharide-stimulated microglia were up-regulated in the GSC supernatant group, which could be reversed by dimethyl amiloride (DMA) (EV secretion inhibitor) co-administration or si-MALAT1 pre-transfection of GSCs. 5-dimethylamiloride 205-208 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 31863766-5 2020 In this study, we found that rapamycin (an mTOR inhibitor) and p70S6K siRNA diminished thrombin-induced IL-8/CXCL8 release. Sirolimus 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 109-114 32010486-6 2020 Upon adding sMICA, the release of cytokines IFN-gamma, TNF-alpha, and IL-8 by NK cell line (NKL) under stimulation of immobilized rMICA was blocked. MHC class I-related chain A 130-135 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 31629806-3 2020 Modulation of basal level and poly(I:C)-induced IL-8 secretion varied between bacterial species, and between heat treated and non-heat treated bacterial cells. Poly I-C 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 31887433-8 2020 The mRNA expression of IL-6, IL-8 and PTGS2 in HT-29 cells decreased by more than 60% upon incubation with CD + SPM138 co-cultures as compared to the levels observed after treatment with CD supernatant only. cd + 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 31887433-9 2020 The concentration of IL-8 also decreased by more than 60% upon treatment with CD + SPM138 co-culture supernatant. cd + 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 31498191-10 2020 RESULTS: Ropivacaine exposure dose-dependently induced apoptosis and an increased release of IL-6, IL-8, and PGE2 from HUVECs and TBs. Ropivacaine 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 31887433-9 2020 The concentration of IL-8 also decreased by more than 60% upon treatment with CD + SPM138 co-culture supernatant. spm138 83-89 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 31498191-14 2020 Conversely, lidocaine exhibited repression of IL-6 and IL-8 release over all time points, and early downregulation of COX2 and cell adhesion molecules, which was followed by a late overshooting reaction. Lidocaine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 32024069-0 2020 Nicotine Induces IL-8 Secretion from Pancreatic Cancer Stroma and Worsens Cancer-Induced Cachexia. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 31855746-6 2020 RESULTS: rDPP dose-dependently reduced the expression of lipopolysaccharide-induced inflammatory genes, such as TNFalpha, IL-1beta, and IL-8, and TNF-alpha protein secretion from the macrophages. rdpp 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 31735734-0 2020 Benzoylaconitine inhibits production of IL-6 and IL-8 via MAPK, Akt, NF-kappaB signaling in IL-1beta-induced human synovial cells. benzoylaconine 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 31735734-2 2020 In this study, the effects and mechanisms of BAC on production of inflammatory cytokines interleukin (IL)-6 and IL-8 were investigated in IL-1beta-stimulated human synovial SW982 cells. 4-deoxyneosamine C 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 31735734-4 2020 The results revealed that BAC suppressed gene and protein expression of IL-6 and IL-8 induced by IL-1beta. 4-deoxyneosamine C 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 31619441-8 2020 However, in the intervention but not the control group, change in urinary PG as a marker of e-cig use and inhalation, was significantly correlated with change in cell counts (cell concentrations, macrophages, and lymphocytes) and cytokines (IL-8, IL-13, and TNF-alpha), although the absolute magnitude of changes was small. Propylene Glycol 74-76 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 31622892-6 2020 PBDEs (47, 99 and 209) exposure decreased TEER, ZO-1 and pH values, and increased IL-8, Muc5AC, Muc5B (mRNAs and proteins), NOX-4 (mRNA), and rheological parameters (G", G"") in ALI cultures of A549 cell line and pHBEC. Halogenated Diphenyl Ethers 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 31769560-9 2020 Pretreatment with BAY 11-7082 significantly inhibited vibration-induced IL-6 and IL-8 mRNA and protein expression in hPDL cells. 3-(4-methylphenylsulfonyl)-2-propenenitrile 18-29 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 32024069-6 2020 Nicotine induced secretion of interleukin 8 (IL-8) by tumor-associated stroma cells in an extracellular signal-regulated kinase (ERK)-dependent fashion. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 32024069-6 2020 Nicotine induced secretion of interleukin 8 (IL-8) by tumor-associated stroma cells in an extracellular signal-regulated kinase (ERK)-dependent fashion. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 31898754-11 2020 However, only IL-8 significantly increased after adding LPS or Poly (I:C) to the AT-MSC media. poly If 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 31821660-10 2020 Extracellular ATP stimulates the secretion of IL8 from epithelial cells to promote the process of in vitro decidualization. Adenosine Triphosphate 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 31634687-4 2020 H295R cells stimulated with either interleukin-1beta (IL-1beta) or phorbol ester also showed elevated IL-8 mRNA levels and higher IL-8 promoter activities. Phorbol Esters 67-80 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 31634687-4 2020 H295R cells stimulated with either interleukin-1beta (IL-1beta) or phorbol ester also showed elevated IL-8 mRNA levels and higher IL-8 promoter activities. Phorbol Esters 67-80 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 31634687-7 2020 Upregulation of IL-8 expression in IL-1beta-treated H295R cells required NF-kappaB while the phorbol ester TPA used both the AP-1 and NF-kappaB sites of the IL-8 gene to stimulate IL-8 expression. Phorbol Esters 93-110 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 31631328-6 2020 Moreover, it was observed that nicotine decreases the production of interleukin (IL)-6 and C-C chemokine ligand (CCL)5 during Mtb infection in epithelial cells (EpCs), whereas in macrophages derived from human monocytes (MDMs) there is a decrease in IL-8, IL-6, tumor necrosis factor (TNF)-alpha, IL-10, CCL2, C-X-C chemokine ligand (CXCL)9 and CXCL10 only during infection with Mtb. Nicotine 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 31372914-6 2020 While conventional amphotericin B further increased IL-6 and to a smaller extent IL-8 levels, this was not the case for its liposomal formulation. Amphotericin B 19-33 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 32080341-10 2020 Pharmacological inhibition of PAP1 with propranolol suppressed UVB-induced production of IL-6 and IL-8 in NHEKs and reconstituted human skin models. Propranolol 40-51 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 31634687-7 2020 Upregulation of IL-8 expression in IL-1beta-treated H295R cells required NF-kappaB while the phorbol ester TPA used both the AP-1 and NF-kappaB sites of the IL-8 gene to stimulate IL-8 expression. Phorbol Esters 93-110 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 31806428-4 2020 RESULTS: In multivariable regression urinary Il-1 alpha correlated positively with podocalyxin and NAG (p < 0.0001, R2= 0.57); urinary IL-8 correlated directly with synaptopodin, NAG, nephrin, and KIM-1 (p < 0.0001, R2 = 0.67); urinary IL-18 correlated directly with synaptopodin, NAG, and nephrin (p < 0.0001, R2 = 0.59). synaptopodin 168-180 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 31135098-6 2020 We also assessed the production of inflammatory factors interleukin-8 and chemokine ligand-2 induced by benzo(a)pyrene exposure at both mRNA and protein levels. Benzo(a)pyrene 104-118 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 31806428-5 2020 Serum IL-1 alpha correlated positively with nephrin, synaptopodin, NAG (P < 0.0001, R2 = 0.68); serum IL-8 correlated directly with synaptopodin and NAG (p < 0.0001, R2 = 0.66); serum IL-18 correlated directly with NAG, KIM-1, and podocalyxin (p < 0.0001, R2=0.647). synaptopodin 135-147 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 31475386-6 2020 The proline mutation in the TMD of beta2 completely inhibited arrest of rolling HL-60 cells in response to the chemokine IL-8. Proline 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 31383073-1 2020 N and F co-doped La-TiO2 (La-TONF) samples were prepared through the solvothermal method by using HMT and NaF as precursors. la-tio2 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 32554850-10 2020 Pretreatment of A-T cells with alpha-LA inhibited IL-1beta-induced activation of NF-kappaB, IL-8 expression, and mitochondrial dysfunction by reducing ROS levels. Thioctic Acid 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 32554850-0 2020 Inhibitory effect of alpha-lipoic acid on mitochondrial dysfunction and interleukin-8 expression in interleukin-1beta-stimulated ataxia teleangiectasia fibroblasts. Thioctic Acid 21-38 C-X-C motif chemokine ligand 8 Homo sapiens 72-85 32554850-4 2020 ROS are related to mitochondrial dysfunction and activation of nuclear factor kappa B (NF-kappaB) to induce IL-8 expression. Reactive Oxygen Species 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 31347162-0 2020 CD73-dependent adenosine dampens interleukin 1beta-induced CXCL8 production in gingival fibroblasts: Association with heme oxygenase-1 and adenosine monophosphate-activated protein kinase. Adenosine 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 59-64 31347162-3 2020 Here, we investigated whether CD73-mediated hydrolysis of extracellular ATP (eATP) could affect interleukin (IL)-1beta-induced CXCL8 secretion. Adenosine Triphosphate 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 127-132 31347162-7 2020 The effect of eATP degradation to adenosine on CXCL8 levels was investigated using agonist and antagonist of adenosine receptors. Adenosine 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 47-52 31347162-9 2020 ATP pretreatment impaired IL-1beta-induced CXCL8 secretion and required activation of heme oxygenase-1 (HO-1) and phosphorylated adenosine monophosphate-activated protein kinase (pAMPK). Adenosine Triphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 31347162-10 2020 The inhibition of CD73 or the inhibition of adenosine receptors abrogated the ATP effect on CXCL8 secretion. Adenosine Triphosphate 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 92-97 31347162-11 2020 CONCLUSIONS: CD73-generated adenosine dampens IL-1beta-induced CXCL8 in HGFs and involves HO-1 and pAMPK signaling. Adenosine 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 63-68 32554850-6 2020 This study is aimed to determine if alpha-LA confers protection against NF-kappaB activation, IL-8 expression, and mitochondrial dysfunction in A-T cells which are exposed to the inflammatory cytokine IL-1beta. Thioctic Acid 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 32554850-11 2020 In conclusion, supplementation with alpha-LA may be beneficial for reducing the oxidative stress-induced mitochondrial dysfunction and IL-8 production associated with A-T. Thioctic Acid 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 31860524-1 2020 OBJECTIVES: Atherosclerotic plaque molecular imaging with F-sodium fluoride (NaF) PET with computed tomography (PET-CT) may identify active unstable microcalcification. Sodium Fluoride 58-75 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 32001775-7 2020 ROS-derived 4-hydroxy-2-nonenal induced interleukin IL-8 release from monocytes. 4-hydroxy-2-nonenal 12-31 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 31639410-5 2020 In nitrogen-mustard-exposed cultured immortalized human keratinocytes (HaCaT cells), Fra-1 in the nucleus functioned as an inhibitor of inflammatory cytokine interleukin (IL)-8. Nitrogen 3-11 C-X-C motif chemokine ligand 8 Homo sapiens 158-176 31757425-7 2020 Moreover, we found that PEPT1 knockdown in differentiated keratinocytes significantly suppressed the influence of a bacterial-derived peptide, muramyl dipeptide (MDP), on the production of proinflammatory cytokine interleukin-8, implying that bacteria-derived oligopeptides can be transported by PEPT1 in advanced differentiated keratinocytes. Acetylmuramyl-Alanyl-Isoglutamine 143-160 C-X-C motif chemokine ligand 8 Homo sapiens 214-227 31757425-7 2020 Moreover, we found that PEPT1 knockdown in differentiated keratinocytes significantly suppressed the influence of a bacterial-derived peptide, muramyl dipeptide (MDP), on the production of proinflammatory cytokine interleukin-8, implying that bacteria-derived oligopeptides can be transported by PEPT1 in advanced differentiated keratinocytes. Acetylmuramyl-Alanyl-Isoglutamine 162-165 C-X-C motif chemokine ligand 8 Homo sapiens 214-227 31680128-5 2020 RESULTS: Fipronil treatment increased pro-inflammatory cytokine interleukin (IL)-1beta, IL-6, IL-8, and MUC5AC expression in human primary nasal epithelial cells. fipronil 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 31680128-9 2020 CONCLUSIONS: Fipronil induced pro-inflammatory cytokine IL-1beta, IL-6, IL-8, and MUC5AC expression via ERK1/2 MAPK, p38 MAPK, and NF-kB in human primary nasal epithelial cells. fipronil 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 31536757-7 2020 Moderate concentrations of PFOS suppressed release of the chemokines CXCL8 and CXCL10, whereas both PFOS and PFOA stimulated the release of the pro-inflammatory cytokine IL-1beta in immune stimulated human bronchial epithelial cells. perfluorooctane sulfonic acid 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 69-74 33329788-8 2020 Results: Curcumin attenuated expression of TNF-alpha, IL-6, and IL-8 and the phosphorylation levels of p38 and JNK, but not ERK1/2, in LPS-stimulated neutrophils. Curcumin 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 31825424-5 2020 They also showed anti-inflammatory potential in tumor necrosis factor (TNF)-alpha-, interleukin (IL)-1beta- and H2O2-stimulated Caco-2 cells by suppressing the secretion of IL-8 and the expression of cyclooxygenase 2 (COX-2) and inducible nitric oxide synthase (iNOS). Water 112-116 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 31971958-8 2020 RESULTS: Dolutegravir reduced inflammation by decreasing NFkappaB activation and IL-6/IL-8/sICAM-1/sVCAM-1 secretion, as did maraviroc with a milder effect. dolutegravir 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 32025384-10 2020 Cholesterol and magnesium intake exerted enhancing effects on the positive relationship between the relative abundance of Comamonas and IL-8 concentration (p < 0.05). Cholesterol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 32025384-10 2020 Cholesterol and magnesium intake exerted enhancing effects on the positive relationship between the relative abundance of Comamonas and IL-8 concentration (p < 0.05). Magnesium 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 31975332-1 2021 BACKGROUND: Microcalcifications cannot be identified with the present resolution of CT; however, 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) imaging has been proposed for non-invasive identification of microcalcification. Sodium Fluoride 97-116 C-X-C motif chemokine ligand 8 Homo sapiens 122-125 31975332-1 2021 BACKGROUND: Microcalcifications cannot be identified with the present resolution of CT; however, 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) imaging has been proposed for non-invasive identification of microcalcification. CP-18 compound 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 122-125 31975332-2 2021 The primary objective of this study was to assess whether 18F-NaF activity can assess the presence and predict the progression of CT detectable vascular calcification. CP-18 compound 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 31975332-3 2021 METHODS AND RESULTS: The data of two longitudinal studies in which patients received a 18F-NaF PET-CT at baseline and after 6 months or 1-year follow-up were used. CP-18 compound 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 31975332-8 2021 CONCLUSION: The activity of 18F-NaF is related to the amount of calcification and calcification progression. CP-18 compound 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 31886641-3 2020 The optimum amount of FEC (10 vol.%) renders a stable LiF/NaF-rich SEI on Sb electrodes that can suppress the continuous electrolytes decomposition and accommodate the volume variation. vinyl fluoride 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 31964911-4 2020 In M0 macrophages, cyH induced a pro-inflammatory phenotype characterized by an increase in TNFalpha and IL-8/MIP-2 secretion. cyclohexanone 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 31886641-3 2020 The optimum amount of FEC (10 vol.%) renders a stable LiF/NaF-rich SEI on Sb electrodes that can suppress the continuous electrolytes decomposition and accommodate the volume variation. Antimony 74-76 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 31928157-8 2020 Medin induced EC immune activation (increased interleukin-8, interleukin-6, intercellular adhesion molecule-1, and plasminogen activator inhibitor-1) and reduced EC viability, which were reversed by monosialoganglioside-containing nanoliposomes. sialogangliosides 199-219 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 31960968-9 2020 RESULTS: We report here that UDCA significantly reduced the IL1beta and TNFalpha-induced expression of IL1, IL6 and IL8 in gingival fibroblasts and the HSC-2 cell line. Ursodeoxycholic Acid 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 31931830-6 2020 From pre- to post-deployment/bTBI, levels of interleukin 8 (IL-8) were decreased among both mild cases (mu = - 83.43 pg/ml; s.e. btbi 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 31931830-6 2020 From pre- to post-deployment/bTBI, levels of interleukin 8 (IL-8) were decreased among both mild cases (mu = - 83.43 pg/ml; s.e. btbi 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 31931830-14 2020 CONCLUSION: The findings of this longitudinal study indicate that in the chronic phase of bTBI, levels of IL-8 and MMP3 may be substantially lower than pre-injury. btbi 90-94 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 31902928-5 2020 Regarding neutrophilic airway inflammation in steroid-resistant asthma, IL-17 derived from Th17 cells and IL-8 and tumor necrosis factor-alpha derived mainly from macrophages were reported to be involved in the pathogenesis. Steroids 46-53 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 31825618-5 2020 Meanwhile, 80 muM kaempferol alleviated the drop of TEER, the increase of FITC flux, and the overexpression of interleukin-8 (IL-8) induced by 1 mug/mL lipopolysaccharide (LPS). kaempferol 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 31825618-5 2020 Meanwhile, 80 muM kaempferol alleviated the drop of TEER, the increase of FITC flux, and the overexpression of interleukin-8 (IL-8) induced by 1 mug/mL lipopolysaccharide (LPS). kaempferol 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 31825618-7 2020 Our results suggest that kaempferol alleviates the IL-8 secretion and barrier dysfunction of the Caco-2 monolayer in the LPS-induced epithelial-endothelial coculture model via inhibiting the NF-kappaB signaling pathway activation. kaempferol 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 33176315-1 2020 The aim of this study was to evaluate the protective effect of propylene glycol alginate (PGA) associated with sodium fluoride (NaF) against enamel erosion and erosion-abrasion. propylene glycol alginate ester 63-88 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 31509822-9 2020 IL-8 and IL-6 clearance were higher with Hemofeel (continuous venovenous hemodiafiltration) than with EMiC2 (continuous venovenous hemodialysis) because the polymethyl methacrylate (PMMA)-based membrane Hemofeel is able to remove these 2 cytokines by adsorption. hemofeel 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 31509822-9 2020 IL-8 and IL-6 clearance were higher with Hemofeel (continuous venovenous hemodiafiltration) than with EMiC2 (continuous venovenous hemodialysis) because the polymethyl methacrylate (PMMA)-based membrane Hemofeel is able to remove these 2 cytokines by adsorption. Polymethyl Methacrylate 157-180 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 31509822-9 2020 IL-8 and IL-6 clearance were higher with Hemofeel (continuous venovenous hemodiafiltration) than with EMiC2 (continuous venovenous hemodialysis) because the polymethyl methacrylate (PMMA)-based membrane Hemofeel is able to remove these 2 cytokines by adsorption. hemofeel 203-211 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 33176315-1 2020 The aim of this study was to evaluate the protective effect of propylene glycol alginate (PGA) associated with sodium fluoride (NaF) against enamel erosion and erosion-abrasion. Sodium Fluoride 111-126 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 31522271-1 2020 PURPOSE: We evaluated the prognostic value of 18F-sodium fluoride (NaF) PET/CT in patients with urological malignancies treated with cabozantinib and nivolumab with or without ipilimumab. 18f-sodium fluoride 46-65 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 32056981-8 2020 Moreover, glucose-containing CM reduced the macrophage secretion of TNFalpha and IL-8 but elevated the IL-12 and IL-23 levels, showing an opposite pattern of distinct pro-inflammatory cytokines modulated by cancer glucose metabolites. Glucose 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 31814524-0 2020 4-phenylbutyric acid promotes migration of gastric cancer cells by histone deacetylase inhibition-mediated IL-8 upregulation. 4-phenylbutyric acid 0-20 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 31814524-6 2020 Based on the expression profile microarray, IL-8 was the most significantly up-regulated gene by 4-PBA, and was selected for further investigation. 4-phenylbutyric acid 97-102 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 31814524-7 2020 Knockdown of IL-8 partially prevented 4-PBA-induced-EMT by blocking the activation of the downstream Gab2-ERK pathway. 4-phenylbutyric acid 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 31814524-8 2020 Furthermore, CHIP assay confirmed that acetyl-H3 directly combined with the promoter region of IL-8 to promote its transcription. acetyl phosphate 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 31814524-9 2020 Therefore, the results of this study demonstrated that 4-PBA-mediated inhibition of HDAC activity could induce EMT in gastric cancer cells via acetyl-histone-mediated IL-8 upregulation, and the downstream Gab2/ERK activation. 4-phenylbutyric acid 55-60 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 31814524-9 2020 Therefore, the results of this study demonstrated that 4-PBA-mediated inhibition of HDAC activity could induce EMT in gastric cancer cells via acetyl-histone-mediated IL-8 upregulation, and the downstream Gab2/ERK activation. acetyl phosphate 143-149 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 31715382-2 2020 Diagnosis of bone metabolic activity is currently through integrating Positron Emission Tomography (PET) with Sodium Fluoride (18F-NaF) biomarkers. Sodium Fluoride 110-125 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 30417790-0 2020 Efficacy of beta-D-mannuronic acid [M2000] on pro-apoptotic process and inflammatory related molecules NFkB, IL-8 and Cd49d using healthy donor PBMC. mannuronic acid 12-34 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 30417790-1 2020 This investigation evaluates the pro-apoptotic and anti-inflammatory effects of beta-D-mannuronic acid [M2000] compared to diclofenac, based on gene expression involved in apoptosis and inflammation process [including Bcl2, NFkappaB, IL-8 and Cd49d] in peripheral blood mononuclear cells [PBMCs] of healthy donors under exvivo conditions. mannuronic acid 80-102 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 32484090-11 2020 These PET scanners are mainly utilized with 18F-sodium-fluoride (NaF), in order to visualize the skeleton and possible changes. 18f-sodium-fluoride 44-63 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 31442679-7 2020 In the correlation analysis, albumin/creatinine ratio was significantly and positively correlated with IP-10/CXCL10, MCP-1/CCL2, MIG/CXCL9, IL-8/CXCL8, TNF, IL-10, and IL-6. Creatinine 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 31442679-7 2020 In the correlation analysis, albumin/creatinine ratio was significantly and positively correlated with IP-10/CXCL10, MCP-1/CCL2, MIG/CXCL9, IL-8/CXCL8, TNF, IL-10, and IL-6. Creatinine 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 145-150 31522271-1 2020 PURPOSE: We evaluated the prognostic value of 18F-sodium fluoride (NaF) PET/CT in patients with urological malignancies treated with cabozantinib and nivolumab with or without ipilimumab. cabozantinib 133-145 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 32071494-4 2020 The aim is to study the pre-analytical variations on the glucose estimation of using sodium fluoride-disodium EDTA (NaF-Na2EDTA) plasma (glycolysis inhibiting anticoagulant) and determine the fact behind the activity of glycolysis inhibition on the same. Glucose 57-64 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 32114586-8 2020 CONCLUSION: Edaravone can improve the neurological function of patients without causing evident adverse reactions, thereby improving quality of life, which may be correlated to decreased serum TNF-alpha and IL-8 levels. Edaravone 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 33118610-9 2020 Moreover, the protein levels of IL-8, TNF-alpha, and PGE2 were considerably reduced in IL-1beta-induced chondrocytes treated with different concentrations of TCA. cinnamaldehyde 158-161 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 32361718-0 2020 Spectrum of false positive 18F-sodium fluoride (NaF) bone PET/CT findings in Oncology imaging; A narrative pictorial review of cases from a single institution. 18f-sodium fluoride 27-46 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 32361718-1 2020 Fluorine-18-sodium fluoride (18F-NaF) is a positron emission tomography (PET) bone imaging agent mainly used for oncology staging but may also be used in the evaluation of benign bone and joint pathology conditions. fluorine-18-sodium fluoride 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 32071494-4 2020 The aim is to study the pre-analytical variations on the glucose estimation of using sodium fluoride-disodium EDTA (NaF-Na2EDTA) plasma (glycolysis inhibiting anticoagulant) and determine the fact behind the activity of glycolysis inhibition on the same. Edetic Acid 85-114 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 30843768-5 2020 Treatment with alpha-tocopherol (10, 100, and 1,000 muM) and ascorbic acid (15, 150, and 1,500 muM) at the same time that the dextrose was added reduced IL-1beta, IL-6, and IL-8 levels in culture media from cells maintained at 5.5 mM dextrose but had no effect on IL-1beta, IL-6, and IL-8 levels in cells exposed to 27.5 mM dextrose. alpha-Tocopherol 15-31 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 31821937-4 2020 The results demonstrated that treatment with xanthone reduced the production of pro-inflammatory cytokines and chemokines including interleukin (IL)-1beta, IL-6, IL-8, and expression of chemokines thymus and activation-regulated chemokine (TARC) and macrophage-derived chemokine (MDC) in tumor necrosis factor (TNF)-alpha and interferon (IFN)-gamma-stimulated HaCaT cells. Xanthones 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 31598775-4 2020 Various storage conditions, that is 4 C or room temperature (RT) and the addition of sodium fluoride (NaF), were compared during storage up to 30 days. Sodium Fluoride 86-101 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 31598775-12 2020 The increase of GHB in HB samples with NaF was significantly lower than that without preservation. Sodium Oxybate 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 30843768-5 2020 Treatment with alpha-tocopherol (10, 100, and 1,000 muM) and ascorbic acid (15, 150, and 1,500 muM) at the same time that the dextrose was added reduced IL-1beta, IL-6, and IL-8 levels in culture media from cells maintained at 5.5 mM dextrose but had no effect on IL-1beta, IL-6, and IL-8 levels in cells exposed to 27.5 mM dextrose. alpha-Tocopherol 15-31 C-X-C motif chemokine ligand 8 Homo sapiens 284-288 30843768-5 2020 Treatment with alpha-tocopherol (10, 100, and 1,000 muM) and ascorbic acid (15, 150, and 1,500 muM) at the same time that the dextrose was added reduced IL-1beta, IL-6, and IL-8 levels in culture media from cells maintained at 5.5 mM dextrose but had no effect on IL-1beta, IL-6, and IL-8 levels in cells exposed to 27.5 mM dextrose. Glucose 126-134 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 30843768-5 2020 Treatment with alpha-tocopherol (10, 100, and 1,000 muM) and ascorbic acid (15, 150, and 1,500 muM) at the same time that the dextrose was added reduced IL-1beta, IL-6, and IL-8 levels in culture media from cells maintained at 5.5 mM dextrose but had no effect on IL-1beta, IL-6, and IL-8 levels in cells exposed to 27.5 mM dextrose. Glucose 126-134 C-X-C motif chemokine ligand 8 Homo sapiens 284-288 30843768-6 2020 However, ebselen treatment reduced IL-1beta, IL-6, and IL-8 levels in cells maintained in either 5.5 or 27.5 mM dextrose. ebselen 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 30843768-5 2020 Treatment with alpha-tocopherol (10, 100, and 1,000 muM) and ascorbic acid (15, 150, and 1,500 muM) at the same time that the dextrose was added reduced IL-1beta, IL-6, and IL-8 levels in culture media from cells maintained at 5.5 mM dextrose but had no effect on IL-1beta, IL-6, and IL-8 levels in cells exposed to 27.5 mM dextrose. Ascorbic Acid 61-74 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 30843768-5 2020 Treatment with alpha-tocopherol (10, 100, and 1,000 muM) and ascorbic acid (15, 150, and 1,500 muM) at the same time that the dextrose was added reduced IL-1beta, IL-6, and IL-8 levels in culture media from cells maintained at 5.5 mM dextrose but had no effect on IL-1beta, IL-6, and IL-8 levels in cells exposed to 27.5 mM dextrose. Ascorbic Acid 61-74 C-X-C motif chemokine ligand 8 Homo sapiens 284-288 31791492-5 2020 Moreover, 1 mug/mL to 10 mug/mL carbon particle treatments disrupted the keratinocyte differentiation, and up-regulated inflammation- and psoriasis-related genes, such as IL-1beta, IL-6, CXCL1, CXCL2, CXCL3, CCL20, CXCL8, and S100A7 and S100A9, respectively. Carbon 32-38 C-X-C motif chemokine ligand 8 Homo sapiens 215-220 32345772-6 2020 We found that RSV infection caused a marked increase in interleukin (IL)-6, IL-8, IL-1beta and tumor necrosis factor (TNF)- alpha production and release, which was concentration-dependently attenuated by EPB treatment. ephedrannin B 204-207 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 32508149-0 2020 The Influence of Hypericin-Mediated Photodynamic Therapy on Interleukin-8 and -10 Secretion in Colon Cancer Cells. hypericin 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 60-81 32508149-1 2020 The aim of this study was to measure the secretion of interleukin (IL)-8 and -10 during an elicited immune response following sublethal doses of hypericin-mediated photodynamic therapy (HY-PDT) in experimental models of residual colon cancer cells in vitro. hypericin 145-154 C-X-C motif chemokine ligand 8 Homo sapiens 54-80 33223648-1 2020 Aim: The aim is to compare the effects of diode laser, GC tooth mousse, and sodium fluoride (NaF) varnish on dentinal hypersensitivity by scanning electron microscopic (SEM) evaluation. Sodium Fluoride 76-91 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 32586185-5 2020 The control and NaF-treated cells were subjected to the influence of SMF with a moderate induction. smf 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 32863303-5 2020 Moreover, the mRNA expression of anti-inflammation cytokine (TGF-beta), tight junction (Occludin, ZO-1) in the jejunum by different ZnO administration were significantly increased compared with the NC group, while mRNA expression of pro-inflammatory (IL-8), membrane channels that transport water (AQP3) and miR-122a were significantly decreased. Zinc Oxide 132-135 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 32444566-12 2020 The secretion of IL-8 in 45% FiO2 with xenon at 32 C was greater than that of other groups. Xenon 39-44 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 31939174-3 2020 In this chapter, we describe a protocol for the analysis of TNBC cell invasion induced by IL-8 in response to proteasome inhibition by bortezomib (BZ). bortezomib 135-145 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 32581181-7 2020 In pretreated gingival fibroblasts and HSC-2 cells, TCA considerably reduced the expression of IL1beta, IL6, and IL8. Taurocholic Acid 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 31939174-3 2020 In this chapter, we describe a protocol for the analysis of TNBC cell invasion induced by IL-8 in response to proteasome inhibition by bortezomib (BZ). bortezomib 147-149 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 31939174-4 2020 Using this approach, we show that BZ increases the invasion ability of TNBC cells, and that the BZ-increased TNBC cell invasion is suppressed by IkappaB kinase (IKK) inhibition, which also decreases the IL-8 expression. bortezomib 96-98 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 31604846-10 2020 Likewise, AR knockdown in androgen-dependent cells induced IL-8 expression, further demonstrating that AR represses IL-8 expression. Androgens 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 31604846-10 2020 Likewise, AR knockdown in androgen-dependent cells induced IL-8 expression, further demonstrating that AR represses IL-8 expression. Androgens 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 33198933-7 2020 After 6 h incubation with MMC, both HCAEC and HITAEC displayed a decrease in IL8 concentration and the mRNA level of IL6 and IL8 compared to control cells. Mitomycin 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 33198933-7 2020 After 6 h incubation with MMC, both HCAEC and HITAEC displayed a decrease in IL8 concentration and the mRNA level of IL6 and IL8 compared to control cells. Mitomycin 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 33198933-10 2020 These findings suggest that the MMC-induced genotoxic stress in endothelial cells derived from different arteries is associated with differential secretion and gene expression of proinflammatory cytokines IL6 and IL8. Mitomycin 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 213-216 32441198-3 2020 In addition, serum levels of TNF-alpha, IL-1beta, IL-6, IL-8, and tumor marker CEA were decreased significantly in omega-3, vitamin D, and co-supplementation of them, compared with baseline. Fatty Acids, Omega-3 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 32894857-9 2020 Five days after the last dose, serum IL-2 and IL-8 levels dropped significantly in the azithromycin group. Azithromycin 87-99 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 32294654-11 2020 RESULTS: Treating cultured hCMEC/D3 human cells with poly IC induced the expression of CXCL1 as well as another chemokine CXCL8. Poly I-C 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 31764599-8 2020 The overall burden of calcium deposition was also significantly correlated with metabolic syndrome (P = 0.002) and 10-year cardiovascular disease risk score (P = 0.004) CONCLUSION: F-NaF uptake is closely related to diabetes mellitus, whereas aortic calcification on CT is closely related to hypertension. Calcium 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 183-186 32454491-7 2020 Furthermore, YiQi GuBen formula suppressed PDGF-BB-induced expression of phosphorylated p65 and the release of inflammatory factors TNF-alpha, IL-1beta, IL-6, and IL-8 in ASMCs. yiqi guben 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 32441198-3 2020 In addition, serum levels of TNF-alpha, IL-1beta, IL-6, IL-8, and tumor marker CEA were decreased significantly in omega-3, vitamin D, and co-supplementation of them, compared with baseline. Vitamin D 124-133 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 32515426-1 2020 PURPOSE: To assess the effects of experimental titanium tetrafluoride (TiF4) varnish and commercial sodium fluoride (NaF) varnish with CO2 laser on enamel hardness. Sodium Fluoride 100-115 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 32515426-6 2020 NaF varnish (2.26%) with CO2 laser (NFL); 6. Carbon Dioxide 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 31888596-7 2019 The group comparison between filtered air and ZnO exposures showed statistically significant increases of neutrophils and interleukin-8 (IL-8), interleukin-6 (IL-6), matrix metalloproteinase (MMP-9) and tissue inhibitors of metalloproteinases (TIMP-1) in sputum starting at the lowest ZnO concentration of 0.5 mg/m3. Zinc Oxide 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 122-135 31705795-2 2020 Using an in vitro model, we previously reported that hyperglycemic levels of glucose induced a pro-inflammatory (IL-1beta, IL-8, RANTES, GRO-alpha), anti-angiogenic (sFlt-1) and anti-migratory profile in a human trophoblast cell line. Glucose 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 31705795-6 2020 Under excess glucose conditions, allopurinol significantly inhibited trophoblast secretion of inflammatory IL-1beta; caspase-1 activity; IL-8; RANTES; and GRO-alpha. Allopurinol 33-44 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 31705795-8 2020 The presence of IL1Ra significantly inhibited excess glucose-induced trophoblast IL-8 and GRO-alpha secretion but had no effect on RANTES or sFlt-1. Glucose 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 31888596-7 2019 The group comparison between filtered air and ZnO exposures showed statistically significant increases of neutrophils and interleukin-8 (IL-8), interleukin-6 (IL-6), matrix metalloproteinase (MMP-9) and tissue inhibitors of metalloproteinases (TIMP-1) in sputum starting at the lowest ZnO concentration of 0.5 mg/m3. Zinc Oxide 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 31888640-7 2019 RESULTS: Ticagrelor and clopidogrel can inhibit the degradation of IKBalpha and phosphorylation of p65, prevent p65 from entering the nucleus, reduce the production of TNFalpha, IL-1, IL-8, IL-6 and IL-2, and alleviate the decrease in cell viability, cell migration and angiogenesis, the changes of cell cycle and apoptosis induced by LPS. Ticagrelor 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 31888640-7 2019 RESULTS: Ticagrelor and clopidogrel can inhibit the degradation of IKBalpha and phosphorylation of p65, prevent p65 from entering the nucleus, reduce the production of TNFalpha, IL-1, IL-8, IL-6 and IL-2, and alleviate the decrease in cell viability, cell migration and angiogenesis, the changes of cell cycle and apoptosis induced by LPS. Clopidogrel 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 31864360-8 2019 RESULTS: CF cells exposed to digitoxin exhibited significant suppression of both TNFalpha/NFkappaB signaling and downstream secretion of IL-8, IL-6 and GM-CSF, with or without co-treatment with VX drugs. Digitoxin 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 31892218-5 2019 The hDPSCs exposed to HEMA let to an increment of ROS formation and in the expression of high levels of inflammatory mediators such as nuclear factor-kappaB (NFkB), inflammatory cytokines such as interleukin IL6, IL8, interferon (IFN)gamma and monocyte chemoattractant protein (MCP)1. poly(2-hydroxyethylmethacrylate)-TiO2 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 213-239 31877842-4 2019 By using a combined salt of 95%NaCl + 5%NaF, an effective liquid reaction medium was formed, greatly facilitating the Al8B4C7 formation. aluminum boride 118-125 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 31877739-10 2019 Cytotoxic effects of P6 peptide, colchicine, and colchicine-P6 peptide on macrophages were compared and the inhibition of ROS generation and interleukin-8 (IL-8) secretion in MSU-stimulated macrophages treated with P6 peptide, colchicine, or colchicine-P6 peptide was studied. Uric Acid 175-178 C-X-C motif chemokine ligand 8 Homo sapiens 141-154 31877739-14 2019 The colchicine-P6 peptide significantly reduced ROS generation and IL-8 secretion compared to the P6 peptide alone at 1 and 10 muM concentrations. Colchicine 4-14 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 31526917-5 2019 CCL2 (p = 0.039), and CCL5 (p = 0.001) levels were significantly higher in fingolimod-treated patients than healthy controls, whereas end-of-study serum levels of IL-6, IL-8, IL-17A, IL-22, IL-23, TNF-alpha, CXCL10, and CXCL13 were comparable to the baseline levels. Fingolimod Hydrochloride 75-85 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 31862943-6 2019 The duration of action of intravitreal dexamethasone implants in DME patients was associated with the level of aqueous IL-8 and the number of HF using OCT. Dexamethasone 39-52 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 31888128-5 2019 The effect of the extracts, diosmin, 1-octen-3-ol on the secretion of pro-inflammatory cytokines, IL-6 (A) and IL-8 (B) by human dermal fibroblasts was significant (p < 0.001). 1-octen-3-ol 37-49 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 31610186-4 2019 Among the 17 flavonoids tested, only apigenin (flavones), luteolin (flavones), daidzein (isoflavones) and genistein (isoflavones) reduced LPS-induced release of inflammatory cytokines/chemokines interleukin (IL)-6, IL-8 and monocyte chemoattractant protein-1 in BEAS-2B cells. Genistein 106-115 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 31610186-5 2019 Quercetin caused further increase in LPS-induced IL-6 and IL-8 levels. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 31610186-8 2019 Apigenin and genistein, but not quercetin, increased the cAMP level in BEAS-2B cells, and the cell-permeable cAMP analogue, 8-Br-cAMP, inhibited LPS-induced increase of IL-8 level. Apigenin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 31851935-3 2019 Metformin interrupts bidirectional signaling between tumor and mesothelial cells by blocking OvCa cell TGF-beta signaling and mesothelial cell production of CCL2 and IL-8. Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 31851935-6 2019 Disruption of HIF1alpha-driven IL-8 signaling in mesothelial cells by metformin results in reduced OvCa invasion in an organotypic 3D model. Metformin 70-79 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 31844123-9 2019 In addition, Sch A decreased the DON-induced cyclooxygenase-2 expression and prostaglandin E2 production and pro-inflammatory cytokine interleukin 8 expression and secretion. schizandrin A 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 135-148 31610186-8 2019 Apigenin and genistein, but not quercetin, increased the cAMP level in BEAS-2B cells, and the cell-permeable cAMP analogue, 8-Br-cAMP, inhibited LPS-induced increase of IL-8 level. Genistein 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 31610186-8 2019 Apigenin and genistein, but not quercetin, increased the cAMP level in BEAS-2B cells, and the cell-permeable cAMP analogue, 8-Br-cAMP, inhibited LPS-induced increase of IL-8 level. Cyclic AMP 109-113 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 31610186-8 2019 Apigenin and genistein, but not quercetin, increased the cAMP level in BEAS-2B cells, and the cell-permeable cAMP analogue, 8-Br-cAMP, inhibited LPS-induced increase of IL-8 level. 8-Bromo Cyclic Adenosine Monophosphate 124-133 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 31811113-4 2019 RESULTS Cells predisposed to MG demonstrated an increase in oxidative stress with augmented (P<0.01) inflammatory cytokines such as cyclooxygenase (COX)-2, chemokine receptor CXCR4, interleukin (IL)-6, IL-8, monocyte chemoattractant protein-1 (MCP-1), and intercellular adhesion molecule 1 (ICAM-1) genes. Pyruvaldehyde 29-31 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 31733592-6 2019 This was demonstrated using the argininocalix[4]arene 1 in miRNA therapeutic approaches performed on three well-described experimental model systems: (1) the induction of apoptosis by antimiR-221 in glioma U251 cells; (2) the induction of apoptosis by premiR-124 in U251 cells; and (3) the inhibition of pro-inflammatory IL-8 and IL-6 genes in cystic fibrosis IB3-1 cells. calix(4)arene 32-53 C-X-C motif chemokine ligand 8 Homo sapiens 321-325 31817562-7 2019 High-glucose conditions increased glucose transporters, glucose influx, ROS, all the high-glucose-induced harmful pathways, TGF-beta1 and IL-8, cell apoptosis, and MMT. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 31849953-8 2019 On the other hand, Toll-like receptor 4 blockade significantly reduced PA-induced IL-8 secretion by osteoblasts, while blocking Toll-like receptor 2 had no effect. Palmitic Acid 71-73 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 31805999-0 2019 PTPRD-inactivation-induced CXCL8 promotes angiogenesis and metastasis in gastric cancer and is inhibited by metformin. Metformin 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 27-32 31824163-9 2019 Supplementation with CoQ10 demonstrated a significant decrease in IL-8 and IL-6 serum levels compared to placebo (P< 0.05). coenzyme Q10 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 31849953-9 2019 In osteoclasts, IL-8 secretion was enhanced by PA and LA particularly at the earliest time point of differentiation. Palmitic Acid 47-49 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 31571042-2 2019 The present study aimed to evaluate the association between carotid 18F-sodium fluoride (NaF) and 18F-fluorodeoxyglucose (FDG) uptake with the severity of ischemic vascular brain disease on MRI in patients with carotid artery disease. Sodium Fluoride 68-87 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 31470141-0 2019 Reversine inhibits MMP-3, IL-6 and IL-8 expression through suppression of ROS and JNK/AP-1 activation in interleukin-1beta-stimulated human gingival fibroblasts. 2-(4-morpholinoanilino)-6-cyclohexylaminopurine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 31297987-11 2019 In THP-1 cell assays, MSU crystals grown with healthy cartilage homogenate increased the release of interleukin-8, whereas MSU crystals grown with type II collagen or albumin had no effect on inflammatory cytokine release. Uric Acid 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 31407195-12 2019 The levels of plasma inflammatory markers were significantly decreased in BA group after 7 days of intervention in TNF-alpha, IL-1beta, IL-6, IL-8, and PGE2. boswellic acid 74-76 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 31751886-10 2019 Besides, Curcumin and Capsaicin down-regulated expression of pro-inflammatory cytokines TNF-alpha, IL-6, and CXCL8/IL-8 and up regulated the expression of IL-10, a sign of lowered M1/M2 ratio relating to abrogation of inflammation. Curcumin 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 109-114 31751886-10 2019 Besides, Curcumin and Capsaicin down-regulated expression of pro-inflammatory cytokines TNF-alpha, IL-6, and CXCL8/IL-8 and up regulated the expression of IL-10, a sign of lowered M1/M2 ratio relating to abrogation of inflammation. Curcumin 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 31751886-10 2019 Besides, Curcumin and Capsaicin down-regulated expression of pro-inflammatory cytokines TNF-alpha, IL-6, and CXCL8/IL-8 and up regulated the expression of IL-10, a sign of lowered M1/M2 ratio relating to abrogation of inflammation. Capsaicin 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 109-114 31751886-10 2019 Besides, Curcumin and Capsaicin down-regulated expression of pro-inflammatory cytokines TNF-alpha, IL-6, and CXCL8/IL-8 and up regulated the expression of IL-10, a sign of lowered M1/M2 ratio relating to abrogation of inflammation. Capsaicin 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 31546097-5 2019 Exposure to HA mineral in scaffolds increased the expression of pro-tumorigenic interleukin-8 (IL-8) among transformed but not benign cells. Durapatite 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 80-93 31546097-5 2019 Exposure to HA mineral in scaffolds increased the expression of pro-tumorigenic interleukin-8 (IL-8) among transformed but not benign cells. Durapatite 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 30997568-11 2019 CLINICAL RELEVANCE: Brushing with a NaF-containing dentifrice can rapidly improve remineralisation, enamel erosion resistance and fluoride uptake. Fluorides 130-138 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 31949929-10 2019 Results: Ex vivo drug treatment of 49 primary gastric cultures from naive patients revealed a significant correlation between basal levels of IL-8 and chemosensitivity to cisplatin (P=0.001) and oxaliplatin (P=0.001). Cisplatin 171-180 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 31612365-4 2019 Therefore, the aim of the study was to investigate influence of NADPH oxidase inhibition on the expression of IL-6, IL-8, TNF, TSLP, CD59, and PPAR-gamma in vitro. NADP 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 31612365-8 2019 The time-response and dose-response study showed that apocynin significantly influenced the relative expression of chosen genes (IL-6, IL-8, TNF, PPAR-gamma, TSLP, and CD59). acetovanillone 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 31949929-11 2019 IL-8 protein expression levels were significantly decreased in the early phase after cisplatin and oxaliplatin treatments leading to an increase in cell sensitivity to drug treatments. Cisplatin 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 31949929-11 2019 IL-8 protein expression levels were significantly decreased in the early phase after cisplatin and oxaliplatin treatments leading to an increase in cell sensitivity to drug treatments. oxaliplatin 99-110 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 31949929-16 2019 The established primary gastric culture could serve as a valuable tool for chemotherapy screening, while the repeated usage of platinum drugs may result in drug resistance via upregulation of IL-8 levels. Platinum 127-135 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 31578786-8 2019 The secretion of SASP components, including interleukin (IL)-8, IL-6, and C-C motif chemokine ligand 2 was also substantially reduced in the presence of PC. Phosphatidylcholines 153-155 C-X-C motif chemokine ligand 8 Homo sapiens 44-62 31424110-1 2019 This study characterized the distribution of [18 F]-sodium fluoride (NaF) uptake and blood flow in the femur and acetabulum in hip osteoarthritis (OA) patients to find associations between bone remodeling and cartilage composition in the presence of morphological abnormalities using simultaneous positron emission tomography and magnetic resonance imaging (PET/MR), quantitative magnetic resonance imaging (MRI) and femur shape modeling. Sodium Fluoride 52-67 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 31866771-5 2019 Results: (1) The levels of hs-CRP, IL-6, and IL-8 were significantly increased in the UAP and AMI groups compared with the CPS group (P < 0.01). 4-Deoxy-2-O-Sulfo-Alpha-L-Threo-Hex-4-Enopyranuronic Acid 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 31147402-1 2019 The aim of this study was to determine if additional 18F-sodium fluoride PET/CT (NaF PET/CT) improves the prognostic accuracy in the initial staging of prostate cancer patients with normal bone scintigraphy undergoing prostatectomy. 18f-sodium fluoride 53-72 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 31639635-5 2019 We observed a dramatic reduction of neutrophils oxidative burst, Fc gamma receptors (FcgammaRs)-mediated degranulation and IL-8 plasma levels already after the first forty-eight hours of therapy with ibrutinib. ibrutinib 200-209 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 31520180-9 2019 The secreted levels of IL-8, TNF-alpha, IL-6 and IL-17A induced by silica particles were also significantly lower from CTGF siRNA-transfected cells than that from normal 16HBE cells (P < 0.05). Silicon Dioxide 67-73 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 31520180-7 2019 The secretions of IL-8, TNF-alpha, IL-6 and IL-17A were also significantly increased by silica particles (P < 0.05). Silicon Dioxide 88-94 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 31639635-9 2019 In conclusion, during the initial phases of ibrutinib therapy, the reduction of IL-8, NE, myeloperoxidase (MPO) levels and oxidative burst negatively impacted on mechanisms involved in neutrophils microbicidal activity. ibrutinib 44-53 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 31515297-11 2019 Notably, combination fenretinide-tocilizumab-reparixin treatment significantly suppressed IL-6 and IL-8 release, stem cell gene expression, and invasion in these diverse CSCE populations. Fenretinide 21-32 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 31515297-11 2019 Notably, combination fenretinide-tocilizumab-reparixin treatment significantly suppressed IL-6 and IL-8 release, stem cell gene expression, and invasion in these diverse CSCE populations. reparixin 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 31808632-8 2019 RESULTS: In the appointment of lercanidipine, there was a more rapid decrease in levels of IL-8, VEGF, MS-1, GM-CSF in serum (21 days), and an improvement in renal function, compared with the group that did not receive nephroprotective therapy. lercanidipine 31-44 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 31885477-6 2019 DB103 inhibited the induced-release of angiogenic factors such as monocyte chemotactic protein-1, interleukin-6 (IL-6) and angiopoietin-2 but not IL-8, while apigenin reduced the IL-6 and IL-8 release. Apigenin 158-166 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 31493545-6 2019 It was found as expected that AgNP induced significant release of IL-1beta, IL-6, IL-8 and TNF-alpha in THP1 monocytes more than the basal level. agnp 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 31493545-8 2019 In TDMs, AgNP and Lipo-AgNP induced IL-8 release (p < .0001), but Lipo-AgNP maintained IL-8 release at levels significantly lower than that of AgNP (p < .01). agnp 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 31493545-8 2019 In TDMs, AgNP and Lipo-AgNP induced IL-8 release (p < .0001), but Lipo-AgNP maintained IL-8 release at levels significantly lower than that of AgNP (p < .01). lipo-agnp 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 31493545-8 2019 In TDMs, AgNP and Lipo-AgNP induced IL-8 release (p < .0001), but Lipo-AgNP maintained IL-8 release at levels significantly lower than that of AgNP (p < .01). lipo-agnp 66-75 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 31493545-8 2019 In TDMs, AgNP and Lipo-AgNP induced IL-8 release (p < .0001), but Lipo-AgNP maintained IL-8 release at levels significantly lower than that of AgNP (p < .01). agnp 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 31779275-6 2019 Transcriptional profiling revealed that various genes coding for cytokines and other proinflammatory proteins were upregulated upon recombinant alpha-MMC treatment in THP-1 cells, including MCP-1, IL-8, IL-1beta, and TNF-alpha. MK 316 144-153 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 31720603-3 2019 It is revealed that the SEI layer contains a large amount of NaF and O-As-O polymer which enables the stable cycling of sodium metal anodes. Sodium 120-126 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. Glutathione 46-59 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. Glutathione 46-59 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. Calcium 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. Calcium 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. Oxygen 130-136 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. Ouabain 169-176 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 31548455-7 2019 Pre-incubation of the cells with BAPTA-AM and L-glutathione increased IL-8 secretion, which indicates that Ca2+ ions and reactive oxygen species are associated with the ouabain-mediated reduction in IL-8 levels. Ouabain 169-176 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 31725301-8 2019 In contrast, the stability of C12GlyNa-containing foams followed the trend NaF > NaCl > NaSCN, which is in agreement with NaF promoting and NaSCN breaking intersurfactant H-bonds. c12glyna 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 31725301-8 2019 In contrast, the stability of C12GlyNa-containing foams followed the trend NaF > NaCl > NaSCN, which is in agreement with NaF promoting and NaSCN breaking intersurfactant H-bonds. c12glyna 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 122-125 31725301-8 2019 In contrast, the stability of C12GlyNa-containing foams followed the trend NaF > NaCl > NaSCN, which is in agreement with NaF promoting and NaSCN breaking intersurfactant H-bonds. sodium thiocyanate 88-93 C-X-C motif chemokine ligand 8 Homo sapiens 122-125 31769424-7 2019 Mechanistically, IL-8-induced myotube atrophy is inhibited by treatment with the CXCR2 antagonist, SB225002, or by treatment with the ERK1/2 inhibitor, U0126. SB 225002 99-107 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 31766770-10 2019 BIRB796 and SB203580 reduced TNFalpha-induced IL-8. SB 203580 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 31769424-7 2019 Mechanistically, IL-8-induced myotube atrophy is inhibited by treatment with the CXCR2 antagonist, SB225002, or by treatment with the ERK1/2 inhibitor, U0126. U 0126 152-157 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 31871502-8 2019 However, IL-12, IP-10, and TNF-alpha had no correlation with DR and DME, whereas there was a significant relationship between IL-8 and DME (1.68 (0.97, 2.40)). dimethylethylsilylimidazole 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 31766770-11 2019 SB203580 reduced LPS-induced IL-8. SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 31766770-12 2019 Fluticasone/formoterol, fluticasone/salmeterol, and fluticasone/BIRB796, but not fluticasone/SB203580 combinations, reduced TNFalpha-induced IL-8 stronger than single treatments. fp 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 31766770-12 2019 Fluticasone/formoterol, fluticasone/salmeterol, and fluticasone/BIRB796, but not fluticasone/SB203580 combinations, reduced TNFalpha-induced IL-8 stronger than single treatments. fp 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 31766770-12 2019 Fluticasone/formoterol, fluticasone/salmeterol, and fluticasone/BIRB796, but not fluticasone/SB203580 combinations, reduced TNFalpha-induced IL-8 stronger than single treatments. fp 52-63 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 31766770-12 2019 Fluticasone/formoterol, fluticasone/salmeterol, and fluticasone/BIRB796, but not fluticasone/SB203580 combinations, reduced TNFalpha-induced IL-8 stronger than single treatments. fp 52-63 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 31766770-13 2019 All combinations including fluticasone/SB203580 reduced LPS-induced IL-8 stronger than single treatments. fp 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 31766770-13 2019 All combinations including fluticasone/SB203580 reduced LPS-induced IL-8 stronger than single treatments. SB 203580 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 31752330-7 2019 Cluster analysis demonstrated that patients from cluster three, with the lowest 25(OH)D levels, presented the lowermost vitamin D intake, IL-10 (1.0 +- 0.9 pg/mL), and IL-12p70 (0.5 +- 0.4 pg/mL), but the highest TNF-alpha (9.1 +- 3.5 pg/mL), IL-8 (55.6 +- 117.1 pg/mL), IL-17A (3.5 +- 2.0 pg/mL), total-cholesterol (193.9 +- 61.4 mg/dL), LDL-cholesterol (127.7 +- 58.2 mg/dL), and Apo-B (101.4 +- 33.4 mg/dL) levels, compared with patients from cluster one. 25(oh)d 80-87 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 31257245-5 2019 The children with RMPP had significantly higher BALF levels of IL-8, IL-17 and TNF-alpha than the children with GMPP (P<0.05), and the elevated levels of IL-17 correlated with the focal size of the lung lesions (P<0.05). rmpp 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 31741329-1 2021 BACKGROUND: Fluoride-18 sodium fluoride (18F-NaF) localizes in microcalcifications in atheroma. Sodium Fluoride 12-39 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 31741329-1 2021 BACKGROUND: Fluoride-18 sodium fluoride (18F-NaF) localizes in microcalcifications in atheroma. CP-18 compound 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 31741329-9 2021 NaF uptake correlated with calcium volume on the baseline scan (P = .60, < .0001 ) and calcium volume increment, especially from 1.0 to 1.5 years (r = .79, P < .0001 ). Calcium 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 31741329-9 2021 NaF uptake correlated with calcium volume on the baseline scan (P = .60, < .0001 ) and calcium volume increment, especially from 1.0 to 1.5 years (r = .79, P < .0001 ). Calcium 90-97 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 31741329-10 2021 Patients with persistently high NaF uptake showed a higher calcium volume increment (0-1.5 years) than patients with low or transiently high NaF uptake. Calcium 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 31741329-12 2021 NaF uptake on the baseline scans and high NaF uptake on the serial scans preceded an increase in calcium volume, especially by 1.0-1.5 years. Calcium 97-104 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 31741329-13 2021 Persistently high NaF uptake was associated with a greater increment in calcium volume than patients with transiently elevated or persistently low fluoride uptake. Calcium 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 31722538-3 2021 Results showed that the levels of Benzo[a]pyrene diol epoxide (BPDE) DNA adduct in blood and IL-8 in serum in case group were significantly higher than those in control group (p < 0.01). benzo(a)pyrene 4,5-epoxide 34-61 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 31585112-11 2019 However, the increased secretion of inflammatory cytokines (IL-6 and IL-8) is sustained and these mediators may be involved in the pathophysiology of bladder toxicity following intravesical epirubicin treatment. Epirubicin 190-200 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 31827376-10 2019 Furthermore, the pretreatment of THP-1 cells with either NAC or a selective EGFR inhibitor significantly blocked DEP-induced IL-8 expression, implying that oxidative stress and subsequent EGFR activation mediated DEP-induced inflammatory response. Acetylcysteine 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 31730488-11 2019 Conditioned medium of IPTD-MSCs treated with a combination of DMOG and TNF-alpha contained higher levels of pro-angiogenic (VEGF, IL-6, and IL-8) compared to controls, promoting angiogenesis of human endothelial cells in vitro. Glyprothiazol 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 31730488-11 2019 Conditioned medium of IPTD-MSCs treated with a combination of DMOG and TNF-alpha contained higher levels of pro-angiogenic (VEGF, IL-6, and IL-8) compared to controls, promoting angiogenesis of human endothelial cells in vitro. dimethyloxallyl glycine 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 31323583-7 2019 We found that DEHP at the indicated concentration plus 50.00muM BaP increased cellular and mitochondrial ROS levels, IL-6 and IL-8 secretions at 24 and 48h as well as MDA levels and GSH-Px activities at 48h, compared to the solvent control. Diethylhexyl Phthalate 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 31323583-7 2019 We found that DEHP at the indicated concentration plus 50.00muM BaP increased cellular and mitochondrial ROS levels, IL-6 and IL-8 secretions at 24 and 48h as well as MDA levels and GSH-Px activities at 48h, compared to the solvent control. Benzo(a)pyrene 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 31739592-7 2019 In addition, celastrol suppressed the release of pro-inflammatory cytokines TNF-alpha and IL-8 in HGC27 and AGS cells, which was reversed by over-expression BGN. celastrol 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 31718684-0 2019 Acetyl-L-Carnitine downregulates invasion (CXCR4/CXCL12, MMP-9) and angiogenesis (VEGF, CXCL8) pathways in prostate cancer cells: rationale for prevention and interception strategies. Acetylcarnitine 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 88-93 31718684-13 2019 ALCAR exerts angiopreventive activities on PCa by reducing production/release of pro angiogenic factors (VEGF, CXCL8, CCL2, angiogenin) and metalloprotease MMP-9. Acetylcarnitine 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 111-116 31708994-7 2019 Initial exposure to H2O2 or TNFalpha enhanced SF senescence and increased mRNA expression of IL6, CXCL8, CCL2 and MMP3 and proteins secretion. Water 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 98-103 31703101-5 2019 Significantly elevated faecal sIgA levels during administration of metformin, and its correlation with the expression of genes associated with immune response (CXCR4, HLA-DQA1, MAP3K14, TNFRSF21, CCL4, ACVR1B, PF4, EPOR, CXCL8) supports a novel hypothesis of strong association between metformin and intestinal immune system, and for the first time provide evidence for altered RNA expression as a contributing mechanism of metformin"s action. Metformin 67-76 C-X-C motif chemokine ligand 8 Homo sapiens 221-226 31708994-9 2019 Treatment of senescent SF with the senolytic drug fenofibrate normalized IL6, CXCL8 and CCL2 mRNA expression. Fenofibrate 50-61 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 31411059-12 2019 mRNA expression of proinflammatory and profibrotic factors (TNF-alpha, IL-1, IL-8, MMP3) was elevated by hyperoxia or etoposide. Etoposide 118-127 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 31741708-7 2019 In NHT cells, phenformin affected cell-viability only at the maximal dose but interestingly it inhibited CXCL8 secretion at all the concentrations not affecting cell-viability. Phenformin 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 105-110 31741708-9 2019 Thus, phenformin exerts anti-cancer effects on both cancer cells (cell death induction) and surrounding normal cells (inhibition of CXCL8 secretion). Phenformin 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 132-137 31684995-10 2019 When we stimulated HCC cells with exogenous IL-8, cell invasion and the levels of integrin beta3, p-PI3K, and p-Akt increased, which could be effectively reversed by adding PI3K inhibitor LY294002. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 188-196 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 31385011-1 2019 PURPOSE: To improve the test-retest reproducibility of coronary plaque 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) uptake measurements. 18f-sodium fluoride 71-90 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 31257011-9 2019 Furthermore, montelukast reduced IL-8 (P<.001) production by LPS-treated human neutrophils. montelukast 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 31496351-9 2019 PMA-induced NETosis directly upregulated the TLR9/NF-kappaB pathway in macrophages and subsequently initiated the release of IL-8. Tetradecanoylphorbol Acetate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 30580454-5 2019 Secretion of interleukin-8 from adipose tissue explants was reduced after saxagliptin (median fold-change from baseline: 0.8 saxagliptin vs 3.3 placebo; P=0.02). saxagliptin 74-85 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 30580454-5 2019 Secretion of interleukin-8 from adipose tissue explants was reduced after saxagliptin (median fold-change from baseline: 0.8 saxagliptin vs 3.3 placebo; P=0.02). saxagliptin 125-136 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 31385012-2 2019 Imaging studies using [18F]-sodium fluoride ([18F]NaF) have found changes in tracer kinetics in animals after subjecting bones to strain, indicating an acute physiological response. [18f]-sodium fluoride 22-43 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 31408726-8 2019 Furthermore, exposure of primary human monocyte-derived DCs (moDC) to 8-oxoG base resulted in significantly enhanced expression of cell surface molecules (CD40, CD86, CD83, HLA-DQ) and augmented the secretion of pro-inflammatory mediators IL-6, TNF and IL-8, whereas it did not considerably influence the production of the anti-inflammatory cytokine IL-10. 8-oxog base 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 31545398-8 2019 The present study also demonstrated that bexarotene exerted an anti-inflammatory effect by downregulating expression of interleukin (IL)-6, IL-8, monocyte chemoattractant protein-1, and high mobility group box-1. Bexarotene 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 31683341-0 2019 Treatment with Metformin and Combination of Metformin Plus Pioglitazone on Serum Levels of IL-6 and IL-8 in Polycystic Ovary Syndrome: A Randomized Clinical Trial. Metformin 44-53 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 31683341-0 2019 Treatment with Metformin and Combination of Metformin Plus Pioglitazone on Serum Levels of IL-6 and IL-8 in Polycystic Ovary Syndrome: A Randomized Clinical Trial. Pioglitazone 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 31683341-14 2019 Combination of metformin and pioglitazone therapy was more effective as compared to metformin alone in reducing the levels of IL-6 and IL-8 as well as insulin resistance in PCOS. Metformin 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 31683341-14 2019 Combination of metformin and pioglitazone therapy was more effective as compared to metformin alone in reducing the levels of IL-6 and IL-8 as well as insulin resistance in PCOS. Pioglitazone 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 31683341-14 2019 Combination of metformin and pioglitazone therapy was more effective as compared to metformin alone in reducing the levels of IL-6 and IL-8 as well as insulin resistance in PCOS. Metformin 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 31065903-5 2019 RESULTS: IL-8 levels were significantly higher in the AqH of patients with BU and FUS than in the AqH of control subjects (p < 0.001 and p < 0.001, respectively). bu 75-77 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 31065903-5 2019 RESULTS: IL-8 levels were significantly higher in the AqH of patients with BU and FUS than in the AqH of control subjects (p < 0.001 and p < 0.001, respectively). fusarubin 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 31437494-7 2019 CBD significantly attenuated LPS-induced NF-kappaB activity, IL-8, and MCP-1 release from macrophages. Cannabidiol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 31546233-3 2019 24 and/or 48 hours exposure to BPA 0.1 nM elicited significant increase of the inflammatory molecules interleukin-6 (IL-6), interleukin-8 (IL-8), Monocyte chemo-attractant protein 1alpha (MCP1alpha) and induced G protein-coupled estrogen receptor 30 (GPR30) levels more than 2-fold both in mature adipocytes and SVF cells. bisphenol A 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 31546233-3 2019 24 and/or 48 hours exposure to BPA 0.1 nM elicited significant increase of the inflammatory molecules interleukin-6 (IL-6), interleukin-8 (IL-8), Monocyte chemo-attractant protein 1alpha (MCP1alpha) and induced G protein-coupled estrogen receptor 30 (GPR30) levels more than 2-fold both in mature adipocytes and SVF cells. bisphenol A 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 31546233-8 2019 Interestingly, the action of BPA on SVF cell growth was mimicked by IL-8 treatment and was reverted by incubation with anti-IL8 antibodies. bisphenol A 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 31546233-8 2019 Interestingly, the action of BPA on SVF cell growth was mimicked by IL-8 treatment and was reverted by incubation with anti-IL8 antibodies. bisphenol A 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 31546233-9 2019 All these data suggest that BPA at 0.1nM, a 10 times lower concentration than environmental exposure, increases the expression of pro-inflammatory cytokines via GPR30 both in mature mammary adipocytes and in SVF cells with a possible involvement of IL-8. bisphenol A 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 249-253 31553301-15 2019 ML1899 enhanced ROS/NO production and up-regulated pro-inflammatory cytokines and chemokine including TNF-alpha, IFN-gamma, IL-6 and IL-8 in macrophages. A 1899 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 31439713-8 2019 Following IL-8 inhibition with its receptor inhibitor Reparixin or siRNA knockdown, LCSC features of HCC cells were repressed and sensitivity of cells to Sorafenib increased significantly. Sorafenib 154-163 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 31439713-9 2019 Furthermore, inflammatory cytokines (IL-8, IL-1beta and IL-11) were also up-regulated upon treatment with HCC approved kinase inhibitors Sorafenib and Regorafenib. Sorafenib 137-146 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 31439713-9 2019 Furthermore, inflammatory cytokines (IL-8, IL-1beta and IL-11) were also up-regulated upon treatment with HCC approved kinase inhibitors Sorafenib and Regorafenib. regorafenib 151-162 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 31545444-6 2019 Consistently, senescent astrocytic CRT cells induced by D-galactose exhibited increases in the levels of IL-6 and IL-8 via NF-kappaB activation, which are major SASP components and inflammatory cytokines. Galactose 56-67 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 30611605-6 2019 18F-Sodium fluoride (18F-NaF) is a promising biological tracer that detects microcalcification related to active disease and cellular necrosis within the vessel wall. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 31393642-6 2019 Mechanistically, EVOO phenols counteracts IkappaB degradation and translocation of NF-kappaB to the nucleus, a transcription factor of essential significance to TSLP and IL-8 transcriptional activity; this is evidenced by immunoblotting. evoo phenols 17-29 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 31214736-6 2019 Besides, IL-8-induced invasion and EMT process of TSCC cells were impeded in the present of the NF-kappaB inhibitor, PDTC or BAY117082. 3-(4-methylphenylsulfonyl)-2-propenenitrile 125-134 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 31437494-10 2019 CBD and dexamethasone treatments reduced the IL-8 level induced by LPS when the cells were treated individually, but showed antagonistic effects when used in combination via MCPIP (monocytic chemotactic protein-induced protein). Cannabidiol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 31437494-10 2019 CBD and dexamethasone treatments reduced the IL-8 level induced by LPS when the cells were treated individually, but showed antagonistic effects when used in combination via MCPIP (monocytic chemotactic protein-induced protein). Dexamethasone 8-21 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 31591201-6 2019 Pretreatment of cultured human microglia from normal adult brains with human recombinant IL-37 (1 to 100 ng/mL) inhibits neurotensin (NT)-stimulated secretion and gene expression of IL-1beta and CXCL8. Neurotensin 121-132 C-X-C motif chemokine ligand 8 Homo sapiens 195-200 31671764-5 2019 Our results revealed that stybenpropol A reduced soluble intercellular cell adhesion molecule-1 (sICAM-1), soluble vascular cell adhesion molecule-1 (sVCAM-1), interleukin-8 (IL-8), and interleukin-1beta (IL-1beta) expression by ELISA, inhibited apoptosis, and accelerated nitric oxide (NO) release in TNF-alpha-treated HUVECs. stybenpropol a 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 160-173 31671764-5 2019 Our results revealed that stybenpropol A reduced soluble intercellular cell adhesion molecule-1 (sICAM-1), soluble vascular cell adhesion molecule-1 (sVCAM-1), interleukin-8 (IL-8), and interleukin-1beta (IL-1beta) expression by ELISA, inhibited apoptosis, and accelerated nitric oxide (NO) release in TNF-alpha-treated HUVECs. stybenpropol a 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 31476115-7 2019 Our results show that APZ and the known DHCR7 inhibitor, AY9944, increase 7-DHC levels in airway epithelial cells and potentiate O3-induced IL-6 and IL-8 expression and cytokine release. Aripiprazole 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 31476115-7 2019 Our results show that APZ and the known DHCR7 inhibitor, AY9944, increase 7-DHC levels in airway epithelial cells and potentiate O3-induced IL-6 and IL-8 expression and cytokine release. trans-1,4-Bis(2-chlorobenzaminomethyl)cyclohexane Dihydrochloride 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 31476115-7 2019 Our results show that APZ and the known DHCR7 inhibitor, AY9944, increase 7-DHC levels in airway epithelial cells and potentiate O3-induced IL-6 and IL-8 expression and cytokine release. Ozone 129-131 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 31476115-9 2019 Additionally, we find that APZ increases O3-induced IL-6 and IL-8 expression in human nasal epithelial cells from male but not female donors. Aripiprazole 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 31476115-9 2019 Additionally, we find that APZ increases O3-induced IL-6 and IL-8 expression in human nasal epithelial cells from male but not female donors. Ozone 41-43 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 31647861-8 2019 Additionally, BITC-induced dying U937 cells released lower levels of chemoattractants, such as IL-8 and MCP-1, when compared to cells undergoing classical apoptosis. benzyl isothiocyanate 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 31591201-6 2019 Pretreatment of cultured human microglia from normal adult brains with human recombinant IL-37 (1 to 100 ng/mL) inhibits neurotensin (NT)-stimulated secretion and gene expression of IL-1beta and CXCL8. Neurotensin 134-136 C-X-C motif chemokine ligand 8 Homo sapiens 195-200 31680969-3 2019 In this study, a pH-responsive micelle based on polycaprolactone-block-poly 2-(dimethylamino)ethyl methacrylate (PCL-PDEM) cationic copolymer was developed to carry short interfering RNA (siRNA) for silencing interleukin 8 (IL-8) gene in hepatoma cancer cells. starch polycaprolactone 48-64 C-X-C motif chemokine ligand 8 Homo sapiens 209-222 31636329-7 2019 Budesonide strongly suppressed the production of neutrophil attractant CXCL8, and promoted epithelial integrity in A549 wild-type cells, while A549 Rho-0 cells displayed reduced corticosteroid sensitivity compared to wild-type cells. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 31636329-8 2019 The reduced corticosteroid responsiveness may be mediated by glycolytic reprogramming, specifically glycolysis-associated PI3K signaling, as PI3K inhibitor LY294002 restored the sensitivity of CXCL8 secretion to corticosteroids in A549 Rho-0 cells. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 156-164 C-X-C motif chemokine ligand 8 Homo sapiens 193-198 31618900-7 2019 In addition to the activation of apoptotic pathways, TRAIL-mediated inflammatory responses were attenuated by GlcN pretreatment reducing nuclear NF-kB levels and the expression of downstream target genes IL-6 and IL-8. Glucosamine 110-114 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 31532197-6 2019 Moreover, Cu current collector with NaF-PVDF protective layer also delivers good cycle stability at 5 mA cm-2 and ultrahigh DOD (80%). Copper 10-12 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 31680969-3 2019 In this study, a pH-responsive micelle based on polycaprolactone-block-poly 2-(dimethylamino)ethyl methacrylate (PCL-PDEM) cationic copolymer was developed to carry short interfering RNA (siRNA) for silencing interleukin 8 (IL-8) gene in hepatoma cancer cells. starch polycaprolactone 48-64 C-X-C motif chemokine ligand 8 Homo sapiens 224-228 31680969-3 2019 In this study, a pH-responsive micelle based on polycaprolactone-block-poly 2-(dimethylamino)ethyl methacrylate (PCL-PDEM) cationic copolymer was developed to carry short interfering RNA (siRNA) for silencing interleukin 8 (IL-8) gene in hepatoma cancer cells. poly(2-(dimethylamino)ethyl methacrylate) 71-111 C-X-C motif chemokine ligand 8 Homo sapiens 209-222 31680969-3 2019 In this study, a pH-responsive micelle based on polycaprolactone-block-poly 2-(dimethylamino)ethyl methacrylate (PCL-PDEM) cationic copolymer was developed to carry short interfering RNA (siRNA) for silencing interleukin 8 (IL-8) gene in hepatoma cancer cells. poly(2-(dimethylamino)ethyl methacrylate) 71-111 C-X-C motif chemokine ligand 8 Homo sapiens 224-228 31591378-8 2019 Functional analysis revealed that treatment of transgenic P2Y12+ U937 cells with the receptor agonist 2-MeSADP induced ERK1/2 and Akt phosphorylation and increased the secretion of the chemokines CXCL2, CXCL7, and CXCL8. methylthio-ADP 102-110 C-X-C motif chemokine ligand 8 Homo sapiens 214-219 31686980-11 2019 Immediately after the marathon race, we observed a negative correlation between IL-8 and daily EI, carbohydrate, fiber, fat, iron, calcium, potassium, and sodium intakes, and higher levels of IL-8 on runners with <3 g/kg/day of carbohydrate intake compared to runners with >5 g/kg/day. Carbohydrates 99-111 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 31686980-11 2019 Immediately after the marathon race, we observed a negative correlation between IL-8 and daily EI, carbohydrate, fiber, fat, iron, calcium, potassium, and sodium intakes, and higher levels of IL-8 on runners with <3 g/kg/day of carbohydrate intake compared to runners with >5 g/kg/day. Iron 125-129 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 31686980-11 2019 Immediately after the marathon race, we observed a negative correlation between IL-8 and daily EI, carbohydrate, fiber, fat, iron, calcium, potassium, and sodium intakes, and higher levels of IL-8 on runners with <3 g/kg/day of carbohydrate intake compared to runners with >5 g/kg/day. Calcium 131-138 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 31686980-11 2019 Immediately after the marathon race, we observed a negative correlation between IL-8 and daily EI, carbohydrate, fiber, fat, iron, calcium, potassium, and sodium intakes, and higher levels of IL-8 on runners with <3 g/kg/day of carbohydrate intake compared to runners with >5 g/kg/day. Potassium 140-149 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 31686980-11 2019 Immediately after the marathon race, we observed a negative correlation between IL-8 and daily EI, carbohydrate, fiber, fat, iron, calcium, potassium, and sodium intakes, and higher levels of IL-8 on runners with <3 g/kg/day of carbohydrate intake compared to runners with >5 g/kg/day. Sodium 155-161 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 31686980-11 2019 Immediately after the marathon race, we observed a negative correlation between IL-8 and daily EI, carbohydrate, fiber, fat, iron, calcium, potassium, and sodium intakes, and higher levels of IL-8 on runners with <3 g/kg/day of carbohydrate intake compared to runners with >5 g/kg/day. Carbohydrates 228-240 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 31545276-10 2019 After GSZD treatment, the adhesive and invasive abilities of MH7A cells were reduced, and secretions of MMPs, IL-6 and IL-8 were also reduced. gszd 6-10 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 31490211-10 2019 Cannabis-plus-cocaine use increased CRP, IL-8 and IL-6/IL-10 ratio, but decreased thiol content, and inflammatory and activated-classic monocyte percentages. Cocaine 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 31377467-6 2019 In in vitro, minocycline reduced cytopathic effects (CPEs), viral protein expressions, viral titers, the levels of interleukin (IL)-6 and IL-8 and relative mRNA expressions of IL-12p40, IL-1beta, and tumor necrosis factor (TNF) after EV71 infection. Minocycline 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 31377467-7 2019 The levels of TNF, IL-1beta, IL-6, and IL-8 decreased with a single dose of minocycline in EV71-infected THP-1 cells. Minocycline 76-87 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 31632299-8 2019 Although the promiscuous TAS2R agonists, quinine and denatonium, inhibited the LPS-induced release of TNF-alpha, CCL3 and CXCL8, diphenidol was inactive. Quinine 41-48 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 31632299-8 2019 Although the promiscuous TAS2R agonists, quinine and denatonium, inhibited the LPS-induced release of TNF-alpha, CCL3 and CXCL8, diphenidol was inactive. denatonium 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 31387121-15 2019 CONCLUSION: MK-7 supplementation tended to increase active calcification measured with 18F-NaF PET activity compared with placebo, but no effect was found on conventional CT. Additional research investigating the interpretation of 18F-NaF PET activity is necessary. vitamin MK 7 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 31387121-15 2019 CONCLUSION: MK-7 supplementation tended to increase active calcification measured with 18F-NaF PET activity compared with placebo, but no effect was found on conventional CT. Additional research investigating the interpretation of 18F-NaF PET activity is necessary. vitamin MK 7 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 235-238 31351299-9 2019 Cell-based assays have shown that TBBPA can induce reactive oxygen species in a concentration-dependent manner, and it promotes the production of inflammatory factors such as TNF alpha, IL-6, and IL-8. tetrabromobisphenol A 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. 3-Aminophenylboronic acid 122-147 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. 3-Aminophenylboronic acid 122-147 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. m-apba 149-155 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. m-apba 149-155 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. m-apba 149-155 C-X-C motif chemokine ligand 8 Homo sapiens 218-221 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. Magnesium Chloride 222-228 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. Magnesium Chloride 222-228 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. (nh 4 ) 230-237 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 31305007-2 2019 Here, the phenomena underlying the adsorption of an anti-human interleukin-8 (anti-IL8) monoclonal antibody (mAb) onto an m-aminophenylboronic acid (m-APBA) ligand in the presence of different mobile-phase modulators (NaF/MgCl 2 /(NH 4 ) 2 SO 4 ) and under different pH values (7.5/8.5/9.0) is investigated. (nh 4 ) 230-237 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 31305007-4 2019 Results show that the adsorption of anti-IL8 mAb to m-APBA is enthalpically driven, corroborating the presence of the reversible esterification reaction between boronic acid or boronates and cis-diol-containing molecules. m-apba 52-58 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 31305007-4 2019 Results show that the adsorption of anti-IL8 mAb to m-APBA is enthalpically driven, corroborating the presence of the reversible esterification reaction between boronic acid or boronates and cis-diol-containing molecules. Boronic Acids 161-173 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 31305007-4 2019 Results show that the adsorption of anti-IL8 mAb to m-APBA is enthalpically driven, corroborating the presence of the reversible esterification reaction between boronic acid or boronates and cis-diol-containing molecules. boronates 177-186 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 31305007-4 2019 Results show that the adsorption of anti-IL8 mAb to m-APBA is enthalpically driven, corroborating the presence of the reversible esterification reaction between boronic acid or boronates and cis-diol-containing molecules. cis-diol 191-199 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 31444999-14 2019 Ponatinib treatment significantly increased plasma VEGF, soluble (s)VEGFR1, sVEGFR2, sTIE2, interferon gamma (IFNgamma), tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-6, IL-8, and IL-10 and decreased sVEGFR2. ponatinib 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 31198997-6 2019 Unlike keratinocytes, normal human fibroblasts expressed high levels of TLR4 mRNA and induced interleukin-8 expression upon stimulation with nickel or cobalt. Nickel 141-147 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 31198997-6 2019 Unlike keratinocytes, normal human fibroblasts expressed high levels of TLR4 mRNA and induced interleukin-8 expression upon stimulation with nickel or cobalt. Cobalt 151-157 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 31247373-6 2019 The influence of selected TLR7 agonists on cytokine production is also reported showing that N-cyclopropyl-2-(trifluoromethyl)quinazolin-4-amine (46) is able to induce increased levels of IL-6 and IL-8. n-cyclopropyl-2-(trifluoromethyl)quinazolin-4-amine 93-144 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 31220426-11 2019 RESULTS: Overall Mo from control subjects exposed to ASA showed increased secretion of IL-1RA, IL-8, MCP-1, and TNF-alpha and Mo from stroke patients showed greater release of IL-1RA and MCP-1. Aspirin 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 31220426-13 2019 In addition, in co-cultures independent of Mo origin, ASA reduced IL-6, IL-8, MCP-1, and TNF-alpha. Aspirin 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 29703573-0 2019 IL-8 negatively regulates ABCA1 expression and cholesterol efflux via upregulating miR-183 in THP-1 macrophage-derived foam cells. Cholesterol 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 29703573-1 2019 OBJECTIVE: Previous studies suggest that IL-8 has an important role in the regulation of cholesterol efflux, but whether miRNAs are involved in this process is still unknown. Cholesterol 89-100 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 29703573-2 2019 The purpose of this study is to explore whether IL-8 promotes cholesterol accumulation by enhancing miR-183 expression in macrophages and its underlying mechanism. Cholesterol 62-73 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 29703573-3 2019 METHODS AND RESULTS: Treatment of THP-1 macrophage-derived foam cells with IL-8 decreased ABCA1 expression and cholesterol efflux. Cholesterol 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 29703573-7 2019 Cholesterol transport assays confirmed that IL-8 dramatically inhibited apolipoprotein AI-mediated ABCA1-dependent cholesterol efflux by increasing miR-183 expression. Cholesterol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 29703573-7 2019 Cholesterol transport assays confirmed that IL-8 dramatically inhibited apolipoprotein AI-mediated ABCA1-dependent cholesterol efflux by increasing miR-183 expression. Cholesterol 115-126 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 29703573-9 2019 CONCLUSION: IL-8 enhances the expression of miR-183, which then inhibits ABCA1 expression and cholesterol efflux. Cholesterol 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 31172286-3 2019 Therefore, we introduce a new technique to assess graft viability using 18F-sodium fluoride (18F-NaF) PET-CT for femoral allografts in reverse total shoulder arthroplasty (RSA). 18f-sodium fluoride 72-91 C-X-C motif chemokine ligand 8 Homo sapiens 97-100 31165327-10 2019 In conclusion, combination of resveratrol and silymarin could significantly inhibit inflammatory effects of histamine on cultured HGFs by reduction of IL-6, IL-8, TPA-1, and TNF-alpha. Resveratrol 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 31065104-7 2019 The Spearman correlation test showed that the concentration of IL-8 in the aqueous humor was significantly associated with the aqueous level of Cu (p = 0.009, r = 0.646) and Se (p = 0.031, r = 0.558). Copper 144-146 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 31517562-7 2019 Fluticasone propionate (FP) and dexamethasone (DEX) suppressed IL-6 and IL-8 production in BEAS-2B cells, but clarithromycin (CAM) failed to do so. Fluticasone 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 31517562-7 2019 Fluticasone propionate (FP) and dexamethasone (DEX) suppressed IL-6 and IL-8 production in BEAS-2B cells, but clarithromycin (CAM) failed to do so. Fluticasone 24-26 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 31517562-7 2019 Fluticasone propionate (FP) and dexamethasone (DEX) suppressed IL-6 and IL-8 production in BEAS-2B cells, but clarithromycin (CAM) failed to do so. Dexamethasone 32-45 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 31517562-7 2019 Fluticasone propionate (FP) and dexamethasone (DEX) suppressed IL-6 and IL-8 production in BEAS-2B cells, but clarithromycin (CAM) failed to do so. Dexamethasone 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 31165327-10 2019 In conclusion, combination of resveratrol and silymarin could significantly inhibit inflammatory effects of histamine on cultured HGFs by reduction of IL-6, IL-8, TPA-1, and TNF-alpha. Silymarin 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 31165327-10 2019 In conclusion, combination of resveratrol and silymarin could significantly inhibit inflammatory effects of histamine on cultured HGFs by reduction of IL-6, IL-8, TPA-1, and TNF-alpha. Histamine 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 31049957-7 2019 RESULTS: Production of IL-6, IL-8, MCP-1, and OPG was significantly increased by Poly I:C or Pam3CSK4 to a similar extent. Poly I-C 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 31593984-5 2019 Results: Treatment with curcumin resulted in a dose- and time-dependent decrease in IL-1beta-induced synthesis of inflammatory cytokines, including IL-6, IL-8, MCP-1, and ICAM-1 at both mRNA and protein levels. Curcumin 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 31001928-10 2019 This study suggests that PBM accelerates tooth movement during molar intrusion, due to modulation of IL-6, IL-8 and IL-1beta during bone remodeling. pbm 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 31579207-0 2019 Diffuse Skeletal Uptake on 18F-Fluoro-2-Deoxy-d-glucose Positron Emission Tomography/Computed Tomography Scan in a Patient with Acute Lymphoblastic Leukemia: A Typical Superscan Pattern Resembling NaF Positron Emission Tomography Scan. 4-fluoro-4-deoxyglucose 27-55 C-X-C motif chemokine ligand 8 Homo sapiens 197-200 31584250-6 2019 AOH significantly reduces IL-1beta transcription after 5 h but shows an increasing tendency on IL-8 transcript levels after long-term exposure (20 h). alternariol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 30772226-1 2019 OBJECTIVES: This study aimed to assess the association between increased lesion peri-coronary adipose tissue (PCAT) density and coronary 18F-sodium fluoride (18F-NaF) uptake on positron emission tomography (PET) in stable patients with high-risk coronary plaques (HRPs) shown on coronary computed tomography angiography (CTA). 18f-sodium fluoride 137-156 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 30772226-10 2019 Lesions with 18F-NaF uptake had higher surrounding PCAT density than those without 18F-NaF uptake (-73 HU; interquartile range -79 to -68 vs. -86 HU; interquartile range -94 to -80 HU; p < 0.001). Fluorine-18 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 31584250-7 2019 In IL-1beta-stimulated cells, AOH (20-40 microm) augments TNF-alpha transcripts while repressing IL-8, IL-6, and IL-1beta transcription as well as IL-8 secretion. alternariol 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 31584250-7 2019 In IL-1beta-stimulated cells, AOH (20-40 microm) augments TNF-alpha transcripts while repressing IL-8, IL-6, and IL-1beta transcription as well as IL-8 secretion. alternariol 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 31363829-7 2019 Among the entire patient population, SUA levels significantly increased 3 months after starting treatment with TNFis (279.5 [84.0] vs. 299.0 [102.0] mumol/l, p < 0.0001), while the levels of CRP, IL-6, IL-8, and MCP-1 significantly decreased. sua 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 31348843-12 2019 Galiellalactone reduced the levels of IL8 and granulocyte macrophage-colony stimulating factor in prostate cancer cells per se. galiellalactone 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 31569368-6 2019 In addition, PhIP-mediated PTHrP up-regulated as well as increased IL-8 secretion in 786-O cells, and then contributed to 786-O-mediated bone resorption. 2-amino-1-methyl-6-phenylimidazo(4,5-b)pyridine 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 30676542-1 2019 OBJECTIVE: The main objectives of this article were to assess the effect of preoperative transdermal fentanyl patch (TFP) on interleukin (IL)-6 and IL-8 levels and pain after laparoscopic cholecystectomy. Fentanyl 101-109 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 31430501-6 2019 GNP-HCIm significantly inhibited proliferation and viability inducing apoptosis of LFs and effectively reduced IL-8 release, viability and M2 polarization in alveolar macrophages. gnp-hcim 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 31048000-14 2019 The COX-2 specific celecoxib was identified as the most potent drug to reduce IL-6, IL-8 and TNF-alpha formation after SM exposures in vitro. Celecoxib 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 31557846-5 2019 The transported polyphenols were able to prevent IL-8 production and suppress the gene expression of proinflammatory mediators (TNF-alpha, ICAM-1, VCAM-1, and COX-2) in the TNF-alpha or oxidized low-density lipoprotein (ox-LDL) treated EA.hy926 cells. Polyphenols 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 31620139-9 2019 Within Bangladeshi 1-year-olds, stunting (as measured by height-for-age z-scores) was found to be associated with IL-8 and TGFbeta expression in PMA-ionomycin stimulated samples. Ionomycin 145-158 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 31407890-7 2019 Concentrations of interleukin (IL)-1beta, IL-6, IL-8, and tumor necrosis factor-alpha in macrophage supernatant increased following 100 mug/mL silica exposure for 24 h. Treatment of AMs with 500 muM FAC decreased both oxidant generation and cytokine release associated with silica exposure, supporting a dependence of these effects on sequestration of cell metal by the particle surface. Silicon Dioxide 143-149 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 31548589-11 2019 The immunomodulatory role of histamine on CCL2 and CXCL8 was detected at the transcript and protein levels. Histamine 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 51-56 31482532-1 2021 BACKGROUND: Uptake of 18F-sodium fluoride (18F-NaF) on positron emission tomography (PET) reflects active calcification. 18f-sodium fluoride 22-41 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 31059760-7 2019 Compared to the treatment with LPS only, LPS/APAP co-exposures induced the production of interleukin (IL)-8, a pro-inflammatory cytokine, but suppressed the secretion of IL-6, a cytokine regulating hepatic regeneration, along with the increase in APAP dosages. Acetaminophen 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 89-107 31411318-5 2019 In this study, we treated hESCs with lipopolysaccharide (LPS) and found that LPS treatment increased the mRNA levels of pro-inflammatory cytokines, such as interleukin (IL)-1beta, IL-6, IL-8, IL-18, and TNFalpha, and the secretion of IL-6. hescs 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 31488175-1 2019 INTRODUCTION: In prostate cancer patients, imaging of bone metastases is enhanced through the use of sodium fluoride positron emission tomography (18F-NaF PET/CT). Sodium Fluoride 101-116 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 31488175-3 2019 In this work, 18F-NaF PET/CT was investigated for response assessment to single fraction stereotactic ablative body radiotherapy (SABR) to bone metastases in prostate cancer patients. sabr 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 31488175-13 2019 CONCLUSION: 18F-NaF PET/CT for response assessment of bone metastases to single fraction SABR indicates high rates of reduction of osteoblastic activity in the tumour and non-tumour bone receiving high doses. sabr 89-93 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 31540059-11 2019 HT29/C1 colonic epithelial cells treated with zerumbone suppressed BFT-induced NF-kappaB signaling and IL-8 secretion. zerumbone 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 31491033-8 2019 An enzyme-linked immunosorbent assay (ELISA)-based cytokine array identified interleukin (IL)-6 and IL-8, which show pleiotropic regulatory effects on lung cancer cells, to be specifically produced in higher amounts by the three types of asbestos-exposed lung fibroblasts than normal lung fibroblasts. Asbestos 238-246 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 30861304-2 2019 Previously, we have shown that silica nanoparticles sized 50 nm (Si50) induce release of CXCL8 and IL-6 from BEAS-2B cells, via mechanisms involving NFkappaB, p38 MAP kinase and TGF-alpha-activated EGF receptor. Silicon Dioxide 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 89-94 30565018-2 2019 Accumulating evidence demonstrates that vitamin C administration ameliorate sodium fluoride (NaF)-induced oxidative stress. Ascorbic Acid 40-49 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 30861304-3 2019 In the present study, the role of ROS-mediated mechanisms in the concentration-dependent Si50 induction of CXCL8 and IL-6 responses was examined. Reactive Oxygen Species 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 107-112 30565018-2 2019 Accumulating evidence demonstrates that vitamin C administration ameliorate sodium fluoride (NaF)-induced oxidative stress. Sodium Fluoride 76-91 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 30565018-3 2019 However, the potentially beneficial effects of vitamin C against NaF-induced cytotoxicity and the underlying molecular mechanisms of this protection are not fully understood. Ascorbic Acid 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 30861304-5 2019 Pre-treatment with the ROS inhibitors N-acetyl cysteine (NAC) and diphenyleneiodonium (DPI) partially attenuated CXCL8 and IL-6 responses to 200 microg/mL, but not to 100 microg/mL Si50. Reactive Oxygen Species 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 113-118 30565018-4 2019 Here, we found that NaF stimulated cytotoxicity, increased mitochondrial reactive oxygen species (mROS) production, and induced apoptosis in F9 embryonic carcinoma cells. Reactive Oxygen Species 73-96 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 30565018-4 2019 Here, we found that NaF stimulated cytotoxicity, increased mitochondrial reactive oxygen species (mROS) production, and induced apoptosis in F9 embryonic carcinoma cells. mros 98-102 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 30565018-6 2019 However, all NaF-induced mitochondrial oxidative injuries were efficiently ameliorated by overexpression of Sirt1 or incubation with Mito-TEMPO (a SOD2 mimetic). MitoTEMPO 133-143 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 30565018-7 2019 Moreover, pretreatment with vitamin C enhanced the expression of Sirt1 and decreased NaF-induced mitochondrial oxidative stress and apoptosis. Ascorbic Acid 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 30861304-5 2019 Pre-treatment with the ROS inhibitors N-acetyl cysteine (NAC) and diphenyleneiodonium (DPI) partially attenuated CXCL8 and IL-6 responses to 200 microg/mL, but not to 100 microg/mL Si50. Acetylcysteine 38-55 C-X-C motif chemokine ligand 8 Homo sapiens 113-118 30565018-10 2019 In summary, our data indicate that Sirt1 plays a pivotal role in the ability of vitamin C to stimulate SOD2 activity and attenuate mitochondrial oxidative stress, which partially through vitamin C receptor in NaF-induced F9 cells injury. Ascorbic Acid 80-89 C-X-C motif chemokine ligand 8 Homo sapiens 209-212 30861304-5 2019 Pre-treatment with the ROS inhibitors N-acetyl cysteine (NAC) and diphenyleneiodonium (DPI) partially attenuated CXCL8 and IL-6 responses to 200 microg/mL, but not to 100 microg/mL Si50. Acetylcysteine 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 113-118 30565018-10 2019 In summary, our data indicate that Sirt1 plays a pivotal role in the ability of vitamin C to stimulate SOD2 activity and attenuate mitochondrial oxidative stress, which partially through vitamin C receptor in NaF-induced F9 cells injury. Ascorbic Acid 187-196 C-X-C motif chemokine ligand 8 Homo sapiens 209-212 30861304-5 2019 Pre-treatment with the ROS inhibitors N-acetyl cysteine (NAC) and diphenyleneiodonium (DPI) partially attenuated CXCL8 and IL-6 responses to 200 microg/mL, but not to 100 microg/mL Si50. diphenyleneiodonium 66-85 C-X-C motif chemokine ligand 8 Homo sapiens 113-118 30861304-5 2019 Pre-treatment with the ROS inhibitors N-acetyl cysteine (NAC) and diphenyleneiodonium (DPI) partially attenuated CXCL8 and IL-6 responses to 200 microg/mL, but not to 100 microg/mL Si50. diphenyleneiodonium 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 113-118 30861304-10 2019 In conclusion, Si50-induced CXCL8 and IL-6 involved both ROS-dependent and ROS-independent mechanisms. Reactive Oxygen Species 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 28-33 31211861-7 2019 The results showed that esculetin suppressed histamine-induced expression and secretion of IL-6, IL-8, and MUC5AC in HNEpCs. esculetin 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 30767875-12 2019 Cerulenin repressed the expressions of IL-6, CCL20 and IL-8 in RASFs stimulated by LTF. Cerulenin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 31211861-7 2019 The results showed that esculetin suppressed histamine-induced expression and secretion of IL-6, IL-8, and MUC5AC in HNEpCs. Histamine 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 31211861-10 2019 Inhibiting NF-kappaB pathway suppressed histamine-induced production of IL-6, IL-8, and MUC5AC in HNEpCs. Histamine 40-49 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 31233937-6 2019 In this study, we report that LPA markedly enhanced IL-6 and CXCL15 (mouse homologue of human IL-8) production in MLO-Y4 cells and that this enhancement was suppressed by the LPA1/3-selective antagonist Ki16425, the Gi/o protein inhibitor PTX or the protein kinase C (PKC) inhibitor sotrastaurin. lysophosphatidic acid 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 31252119-4 2019 Moreover, ROS accelerate the translocation and phosphorylation of NF-kappaB in nucleic and promote the expression of inflammatory, such as IL-8 and IL-6. Reactive Oxygen Species 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 31441829-2 2019 METHODS: Comfilcon A, balafilcon A, omafilcon A, and etafilcon A were soaked in 500 and 100 pg/mL of interleukin-8 (IL-8), matrix metalloproteinase-9 (MMP-9), or interleukin-1 receptor antagonist (IL-1Ra), and also in combined solutions of inflammatory mediators (500 pg/mL or 100 pg/mL) separately. etafilcon 53-64 C-X-C motif chemokine ligand 8 Homo sapiens 101-114 31441829-8 2019 There were no differences in IL-8 absorption between lenses; however, more IL-8 remained firmly bound to omafilcon A (P=0.01; 336+-25 pg/mL) than etafilcon A (106+-133 pg/mL) when soaked in 500 pg/mL. omafilcon a 105-116 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 30692654-11 2019 Tamoxifen decreased breast tissue levels of IL-8 and IL-18. Tamoxifen 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 31441829-10 2019 When the mediators were combined, IL-8 was absorbed more in etafilcon A (P=0.03) than in other lens materials, but the absorbed IL-8 did not remain firmly bound. etafilcon 60-71 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 31233937-6 2019 In this study, we report that LPA markedly enhanced IL-6 and CXCL15 (mouse homologue of human IL-8) production in MLO-Y4 cells and that this enhancement was suppressed by the LPA1/3-selective antagonist Ki16425, the Gi/o protein inhibitor PTX or the protein kinase C (PKC) inhibitor sotrastaurin. 3-(4-(4-((1-(2-chlorophenyl)ethoxy)carbonyl amino)-3-methyl-5-isoxazolyl) benzylsulfanyl) propanoic acid 203-210 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 31233937-6 2019 In this study, we report that LPA markedly enhanced IL-6 and CXCL15 (mouse homologue of human IL-8) production in MLO-Y4 cells and that this enhancement was suppressed by the LPA1/3-selective antagonist Ki16425, the Gi/o protein inhibitor PTX or the protein kinase C (PKC) inhibitor sotrastaurin. ptx 239-242 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 31233937-6 2019 In this study, we report that LPA markedly enhanced IL-6 and CXCL15 (mouse homologue of human IL-8) production in MLO-Y4 cells and that this enhancement was suppressed by the LPA1/3-selective antagonist Ki16425, the Gi/o protein inhibitor PTX or the protein kinase C (PKC) inhibitor sotrastaurin. sotrastaurin 283-295 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 31299413-3 2019 We now show mechanistically that EC activation induces the secretion of interleukin-8 (IL-8) leading to significant expansion of non-adherent AML cells and resistance to cytarabine (Ara-C). Cytarabine 182-187 C-X-C motif chemokine ligand 8 Homo sapiens 72-85 31009103-5 2019 Eriodictyol significantly reduced RA-FLS secretion of tumor necrosis factor alpha, interleukin 6 (IL-6), IL-8, and IL-1beta. eriodictyol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 32821713-1 2019 Objective: The objective of this study was to analyze uptake patterns and intensity of 18F-fluorodeoxyglucose (FDG) and 18F-sodium fluoride (NaF) radioligands in carotid atheroma among stroke patients according to carotid atheroma characteristics. 18f-sodium fluoride 120-139 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 32821713-6 2019 FDG uptake at symptomatic carotid arteries was significantly more increased than that at asymptomatic arteries (TBR: 1.17+-0.23 vs. 1.01+-0.15, Mann-Whitney U-test, p=0.02), but NaF uptake was not different (TBR: 1.38+-0.49 vs. 1.51+-0.40, p=0.40). Fluorodeoxyglucose F18 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 31299413-3 2019 We now show mechanistically that EC activation induces the secretion of interleukin-8 (IL-8) leading to significant expansion of non-adherent AML cells and resistance to cytarabine (Ara-C). Cytarabine 170-180 C-X-C motif chemokine ligand 8 Homo sapiens 72-85 31299413-3 2019 We now show mechanistically that EC activation induces the secretion of interleukin-8 (IL-8) leading to significant expansion of non-adherent AML cells and resistance to cytarabine (Ara-C). Cytarabine 182-187 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 31299413-3 2019 We now show mechanistically that EC activation induces the secretion of interleukin-8 (IL-8) leading to significant expansion of non-adherent AML cells and resistance to cytarabine (Ara-C). Cytarabine 170-180 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 31452801-12 2019 Reverse transcription-quantitative PCR analysis performed on docetaxel-sensitive and docetaxel-resistant prostate cancer cell lines demonstrated that certain hub genes, including CDK1, 2"-5"-oligoadenylate synthetase 3, CXCL8 and CDH1, were highly expressed in the docetaxel-resistant cell lines, which confirmed the bioinformatics results. Docetaxel 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 220-225 31283028-10 2019 There was a significant decrease in the serum interleukin-8(IL-8), interleukin-4(IL-4), and eotaxin levels following 3 weeks of clarithromycin therapy. Clarithromycin 128-142 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 31283028-10 2019 There was a significant decrease in the serum interleukin-8(IL-8), interleukin-4(IL-4), and eotaxin levels following 3 weeks of clarithromycin therapy. Clarithromycin 128-142 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 31283028-12 2019 The macrolides may reduce the IL-8 levels in the airway and plasma, but failed to demonstrate an antiviral effect in children with bronchiolitis. Macrolides 4-14 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 31349755-7 2019 Cytochalasin D and amiloride treatment of differentiated THP-1 cells reduced cell-associated MWCNTs and IL-8 induction. Amiloride 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 31452801-12 2019 Reverse transcription-quantitative PCR analysis performed on docetaxel-sensitive and docetaxel-resistant prostate cancer cell lines demonstrated that certain hub genes, including CDK1, 2"-5"-oligoadenylate synthetase 3, CXCL8 and CDH1, were highly expressed in the docetaxel-resistant cell lines, which confirmed the bioinformatics results. Docetaxel 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 220-225 31452801-12 2019 Reverse transcription-quantitative PCR analysis performed on docetaxel-sensitive and docetaxel-resistant prostate cancer cell lines demonstrated that certain hub genes, including CDK1, 2"-5"-oligoadenylate synthetase 3, CXCL8 and CDH1, were highly expressed in the docetaxel-resistant cell lines, which confirmed the bioinformatics results. Docetaxel 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 220-225 31480533-9 2019 The produced EGCG microparticles reduced the expression of inflammatory (IL-6, IL-8, COX-2) and catabolic (MMP1, MMP3, MMP13) mediators in pro-inflammatory 3D cell cultures. epigallocatechin gallate 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 31543817-10 2019 The muscarinic receptor antagonist (MRA) tiotropium, but not aclidinium, caused minor inhibition of the endotoxin-induced release of IL-26 and IL-8, paralleled by a decreased phosphorylation of NF-kappaB. tiotropium 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 31543817-9 2019 The glucocorticoid hydrocortisone caused substantial inhibition of the endotoxin-induced release of IL-26, IL-6, and IL-8, an effect paralleled by a decrease of the phosphorylation of NF-kappaB, p38, and ERK1/2. Hydrocortisone 19-33 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 30542936-10 2019 Additionally, before sleep nNO was also positively associated with IL-6 (r = 0.586, p = 0.005) and IL-8 (r = 0.520, p = 0.016) concentration. Nitrous Oxide 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 31480284-0 2019 Disruption of the NF-kappaB/IL-8 Signaling Axis by Sulconazole Inhibits Human Breast Cancer Stem Cell Formation. sulconazole 51-62 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 31480284-5 2019 Sulconazole inhibited mammosphere formation, reduced the protein level of nuclear NF-kappaB, and reduced extracellular IL-8 levels in mammospheres. sulconazole 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 31480284-7 2019 Sulconazole reduced nuclear NF-kappaB protein levels and secreted IL-8 levels in mammospheres. sulconazole 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 31480284-8 2019 These new findings show that sulconazole blocks the NF-kappaB/IL-8 signaling pathway and CSC formation. sulconazole 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 31469844-4 2019 RESULTS: AL tissues had elevated levels of TNF-family members sTNFR2, TNFSF14, sFasL, sBAFF, cytokines/chemokines IL8, CCL2, IL1RA/IL36, sIL6R, and growth factors sAREG, CSF1, comparing to non-AL. Aluminum 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 114-117 31543817-11 2019 The beta2-adrenoceptor agonist salbutamol caused modest inhibition of the endotoxin-induced release of IL-26 and IL-8, paralleled by a decreased phosphorylation of NF-kappaB, JNK1-3, and p38. Albuterol 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 31531360-8 2019 Our results demonstrated that quercetin inhibited the LPS-induced production of IL-1beta, IL-6, IL-8, and TNF-alpha in a dose-dependent manner. Quercetin 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 31429784-15 2019 Expression of CXCL1 and IL-8 in human endothelial cells was enhanced by LPA, but was inhibited by LA-01. lysophosphatidic acid 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 31534438-6 2019 We found that poly I:C induced increased expression of the proinflammatory cytokines IL1beta, IL6, CXCL8, and TNF and IFN-beta1 in AECs from both control subjects and COPD patients. Poly I-C 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 31443599-0 2019 TNF-alpha in Combination with Palmitate Enhances IL-8 Production via The MyD88- Independent TLR4 Signaling Pathway: Potential Relevance to Metabolic Inflammation. Palmitates 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 31443599-5 2019 We found that co-stimulation of human monocytes with palmitate and TNF-alpha led to increased IL-8 production as compared to those stimulated with palmitate or TNF-alpha alone. Palmitates 53-62 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 31443599-11 2019 These findings suggest that the signaling cross-talk between saturated fatty acid palmitate and TNF-alpha may be a key driver in obesity-associated chronic inflammation via an excessive production of IL-8. saturated fatty acid palmitate 61-91 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 31531360-11 2019 In conclusion, these results suggested that quercetin attenuated the production of IL-1beta, IL-6, IL-8, and TNF-alpha in P. gingivalis LPS-treated HGFs by activating PPAR-gamma which subsequently suppressed the activation of NF-kappaB. Quercetin 44-53 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 31429784-15 2019 Expression of CXCL1 and IL-8 in human endothelial cells was enhanced by LPA, but was inhibited by LA-01. la-01 98-103 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 31409858-0 2019 DF2726A, a new IL-8 signalling inhibitor, is able to counteract chemotherapy-induced neuropathic pain. df2726a 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 31415645-9 2019 Finally, a combined panel of IL-8, IL-15 and gender demonstrated diagnostic accuracy (AUC = 0.830, p < 0.0001) in distinguishing PDAC in the presence of jaundice from benign controls with either jaundice, choledocholithiasis or common bile duct injury. pdac 132-136 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 31313775-4 2019 The calculated results for the ionic structure indicate that molten 1.3(KF + NaF)-AlF3 electrolytes have a high ionic polymerization degree, which is unfavorable for the transport properties of low-temperature 1.3(KF + NaF)-AlF3 electrolytes. lysylphenylalanine 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 31313775-4 2019 The calculated results for the ionic structure indicate that molten 1.3(KF + NaF)-AlF3 electrolytes have a high ionic polymerization degree, which is unfavorable for the transport properties of low-temperature 1.3(KF + NaF)-AlF3 electrolytes. lysylphenylalanine 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 219-222 31409858-4 2019 Exposure to oxaliplatin triggers alterations in peripheral neuropathic pathways previously linked to IL-8 pathway. Oxaliplatin 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 31409858-5 2019 We investigated a novel selective inhibitor of IL-8 receptors, DF2726A, and showed its effects in counteracting CINP pathways, extending the relevance of the activation of IL-8 pathway to the class of platinum chemotherapeutics. df2726a 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 31399091-11 2019 In sputum, compared with placebo both CHF6001 doses significantly decreased leukotriene B4, C-X-C motif chemokine ligand 8, macrophage inflammatory protein 1beta, matrix metalloproteinase 9, and tumour necrosis factor alpha (TNFalpha). 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(cyclopropylmethoxy)-4-(methylsulfonamido)benzoyloxy)ethyl)pyridine 1-oxide 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 76-161 31447857-7 2019 The P2Y11 receptor agonist ATPgammaS and NAD+ could independently stimulate the production of IL-8 in M2 macrophages, however, only the ATPgammaS-induced response was mediated by P2Y11 receptor. adenosine 5'-O-(3-thiotriphosphate) 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 31447857-7 2019 The P2Y11 receptor agonist ATPgammaS and NAD+ could independently stimulate the production of IL-8 in M2 macrophages, however, only the ATPgammaS-induced response was mediated by P2Y11 receptor. NAD 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 30884982-8 2019 Travatan and Lumigan 0.03% increased concentrations of Interleukin (IL)-6 and IL-8 in culture media. Travoprost 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 30905242-1 2019 Objective: The objective of this study was to compare the remineralizing effect of sodium fluoride (NaF) mouth rinse or NaF gel as an adjunct to NaF dentifrice on incipient caries-like lesions in an in situ cross-over design study, with three sessions of 30 days each. Sodium Fluoride 83-98 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 30874442-5 2019 Key contributions from COPDGene include identification of DNA methylation effects from smoking and genetic variation, new transcriptomic signatures in the blood, identification of protein biomarkers associated with severity and progression (e.g., sRAGE [soluble receptor for advanced glycosylation end products], inflammatory cytokines IL-6 and IL-8), and identification of small molecules (ceramides and sphingomyelin) that may be pathogenic. copdgene 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 345-349 30690929-7 2019 The study demonstrated a correlation between venular retinal blood oxygen saturation and proangiogenic factors HGF (r = 0.558, p = 0.038), Ang2 (r = 0.556, p = 0.039) and EGF (r = -0.554, p = 0.040), but did not find any correlation for IL-8 (r = 0.330, p = 0.249) even though this biomarker was significantly higher in the diabetic group. Oxygen 67-73 C-X-C motif chemokine ligand 8 Homo sapiens 237-241 31211863-11 2019 An increased mRNA expression of IL-6, IL-8, and MCP-1 by FAEEs is key finding to suggest a metabolic basis of EtOH-induced inflammatory response. Ethanol 110-114 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 30884982-8 2019 Travatan and Lumigan 0.03% increased concentrations of Interleukin (IL)-6 and IL-8 in culture media. Bimatoprost 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 31005727-8 2019 In presence of OSCC an increased concentration of IL-8(p = 0.004), IL-6(p = 0.005), VEGF(p = 0.014), MIP-1ss(p = 0.033), IP-10(p = 0.047), IL-1beta(p = 0.049) was observed; conversely the concentration of IFN-gamma(p = 0.036) and IL-5(P = 0.048) decreased. oscc 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 31172435-5 2019 Among the three types of SOA, m-xylene-derived SOA showed the strongest induction of the HMOX1 and IL8 genes, and transcriptional activity via the antioxidant response element (ARE). Xylenes 32-38 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 30902292-3 2019 In addition, the glycated TM by glucose, maltotriose, maltopentaose and maltoheptaose inhibited the proliferation and IL-8 secretion of Caco-2, and the CD63 and CD203c expression, MAPK signaling of KU812 basophils, while the glycated TM by maltose had insignificant suppression on the allergy reactivities of Caco-2 cells and KU812 basophils. Glucose 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 30902292-3 2019 In addition, the glycated TM by glucose, maltotriose, maltopentaose and maltoheptaose inhibited the proliferation and IL-8 secretion of Caco-2, and the CD63 and CD203c expression, MAPK signaling of KU812 basophils, while the glycated TM by maltose had insignificant suppression on the allergy reactivities of Caco-2 cells and KU812 basophils. maltotriose 41-52 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 30902292-3 2019 In addition, the glycated TM by glucose, maltotriose, maltopentaose and maltoheptaose inhibited the proliferation and IL-8 secretion of Caco-2, and the CD63 and CD203c expression, MAPK signaling of KU812 basophils, while the glycated TM by maltose had insignificant suppression on the allergy reactivities of Caco-2 cells and KU812 basophils. maltoheptaose 72-85 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 30971437-6 2019 IPE supplementation decreased proinflammatory interleukin-8 levels compared with cellulose, while inulin had no impact on the systemic inflammatory markers studied. ipe 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 30472681-8 2019 In humans, preoperative administration of prucalopride, but not of VNS, decreased Il6 and Il8 expression in the muscularis externa and improved clinical recovery. prucalopride 42-54 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 30738171-10 2019 GBR 830 induced significant progressive reductions in TH1 (IFN-gamma/CXCL10), TH2 (IL-31/CCL11/CCL17), and TH17/TH22 (IL-23p19/IL-8/S100A12) mRNA expression in lesional skin. gbr 830 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 31356535-12 2019 The IL-6 and IL-8 concentrations in the DEX group were dramatically increased at 6 hours after CPB (P < 0.05). Dexmedetomidine 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 31017309-7 2019 A significant (P < 0.05) release of interleukin-8 was observed after Ap exposure to ZnO NPs at 100 mug/mL and after Bl exposure to sono ZnO NPs at 100 mug/mL. Zinc Oxide 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 30558829-11 2019 SB203580 showed little effect on IL-1beta-induced sICAM-1 secretion, but effectively inhibited its induction of IL-8 secretion in pulp cells. SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 31313790-5 2019 Exposure to As(iii) and As(v) generates an increase in the release of the pro-inflammatory cytokine IL-8 (57-1135%) and an increase in the generation of reactive oxygen and/or nitrogen species (130-340%) in both cell lines. Arsenic 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 31158307-0 2019 Human alpha defensins promote the expression of the inflammatory cytokine interleukin-8 under high-glucose conditions: Novel insights into the poor healing of diabetic foot ulcers. Glucose 99-106 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 30515817-5 2019 IL-6 and IL-8 upregulation were blocked by broad-acting HDAC inhibitors SAHA and LBH589. Panobinostat 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 31112773-2 2019 We analyzed impact of this diversity, in relation to carriage and expression of cytholethal distending toxin B (cdtB), on alteration of IL-8, TNF-alpha, TLR2, TLR4, TLR5, CASP3 mRNA and cytokine levels in HT-29 cell line. cytholethal 80-91 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 31272325-2 2019 Two tracers of recent interest for carotid plaque imaging are 18F-fluorodeoxyglucose (18F-FDG) and 18F-sodium fluoride (18F-NaF). 18f-sodium fluoride 99-118 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 31456857-1 2019 Purpose: To determine the utility of 18F-sodium fluoride positron emission tomography-computed tomography (18F-NaF PET/CT) in the imaging assessment of therapy response in men with osseous-only metastatic prostate cancer. 18f-sodium fluoride 37-56 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 30919009-11 2019 alpha-ZOL + beta-ZOL showed antagonistic effects on inflammation for IL-1beta and TNF-alpha, but act synergic for IL-8 at high toxin concentrations. zearalenol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 30919009-11 2019 alpha-ZOL + beta-ZOL showed antagonistic effects on inflammation for IL-1beta and TNF-alpha, but act synergic for IL-8 at high toxin concentrations. zearalenol 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 31357568-5 2019 L-PRPs prepared at 100x g and 100 + 400x g released higher levels of transforming growth factor (TGF)-beta1 and platelet-derived growth factor (PDGF)-BB due to the increased platelet concentration, while inflammatory cytokines interleukin (IL)-8 and tumor necrosis factor (TNF)-alpha were more significantly released from L-PRPs prepared via two centrifugation steps (100 + 400x g and 800 + 400x g) due to the increased concentration of leukocytes. l-prps 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 227-245 31357693-3 2019 The results showed that 1.0 mM H2O2 pre-exposure for 3 h significantly decreased cell viability, and increased interleukin 8 (IL-8) secretion and the intracellular reactive oxygen species (ROS) level. Hydrogen Peroxide 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 31357693-6 2019 Furthermore, the IL-8 secretion and ROS level were significantly blocked by RDE, accompanied by the enhanced gene expression of hemeoxygenase-1 (HO-1), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px), and the enhanced protein expression of the nuclear factor (erythroid-derived 2)-like 2 (Nrf-2). Glutathione 208-211 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 31357693-3 2019 The results showed that 1.0 mM H2O2 pre-exposure for 3 h significantly decreased cell viability, and increased interleukin 8 (IL-8) secretion and the intracellular reactive oxygen species (ROS) level. Hydrogen Peroxide 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 31277614-7 2019 The potential for succinic acid to have anti-inflammatory effects was assessed by measuring the release of inflammatory cytokines IL-1alpha, IL-1beta, IL-8 and TNFalpha, and the inflammatory messenger PGE2, from THP-1 human macrophages after treatment with succinic acid and LPS. Succinic Acid 18-31 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 31324844-5 2019 Production of TNF-alpha, IL-1ss, IL-1RA, MCP-1 and IL-8 was assessed upon addition of 200 microM UA, 500 microM UA or monosodium urate (MSU) crystals in the presence or absence of 5 ng/ml lipopolysaccharide (LPS). Uric Acid 136-139 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 30978440-0 2019 Cancer-associated fibroblasts-derived IL-8 mediates resistance to cisplatin in human gastric cancer. Cisplatin 66-75 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 30978440-2 2019 We identified the high pretherapeutical serum IL-8 level in gastric cancer patients was associated with poor response to platinum-based therapy, and it increased gradually during neoadjuvant chemotherapy and it decreased after radical surgery. Platinum 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 30978440-5 2019 IL-8 increased the IC50 of cisplatin (CDDP) in AGS or MGC-803 in vitro. Cisplatin 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30978440-5 2019 IL-8 increased the IC50 of cisplatin (CDDP) in AGS or MGC-803 in vitro. cddp 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30978440-5 2019 IL-8 increased the IC50 of cisplatin (CDDP) in AGS or MGC-803 in vitro. mgc-803 54-61 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 31241125-4 2019 (2) Dietary putrescine increased the lysozyme and acid phosphatase activities and the amount of immunoglobulin M, antibacterial peptides, and transforming growth factor beta1, but decreased the mRNA levels of tumor necrosis factor alpha, interleukin-6, interleukin-8 and inducible nitric oxide synthase (P < 0.05). Putrescine 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 253-266 31354900-0 2019 Corrigendum to "Cafestol Inhibits Cyclic-Strain-Induced Interleukin-8, Intercellular Adhesion Molecule-1, and Monocyte Chemoattractant Protein-1 Production in Vascular Endothelial Cells". cafestol 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 31278356-6 2019 Kinetic cell viability testing showed that 500 mug/mL of moxifloxacin exposure induced significant decrease (29%) in the viability as early as 1 h. When the inflammatory effects of the antibiotics were examined, a significant induction of IL-8 was observed especially by RVECs after exposure to cefuroxime or vancomycin which was exacerbated by L-alanyl-gamma-D-glutamyl-meso-diaminopimelic acid (Tri-DAP), a NOD1 ligand. Moxifloxacin 57-69 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 31278356-6 2019 Kinetic cell viability testing showed that 500 mug/mL of moxifloxacin exposure induced significant decrease (29%) in the viability as early as 1 h. When the inflammatory effects of the antibiotics were examined, a significant induction of IL-8 was observed especially by RVECs after exposure to cefuroxime or vancomycin which was exacerbated by L-alanyl-gamma-D-glutamyl-meso-diaminopimelic acid (Tri-DAP), a NOD1 ligand. Cefuroxime 295-305 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 31278356-6 2019 Kinetic cell viability testing showed that 500 mug/mL of moxifloxacin exposure induced significant decrease (29%) in the viability as early as 1 h. When the inflammatory effects of the antibiotics were examined, a significant induction of IL-8 was observed especially by RVECs after exposure to cefuroxime or vancomycin which was exacerbated by L-alanyl-gamma-D-glutamyl-meso-diaminopimelic acid (Tri-DAP), a NOD1 ligand. Vancomycin 309-319 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 31333667-4 2019 PolyI:C increased the expression of interferon-beta (IFN-beta), interleukin-6 (IL-6), interleukin-8 (IL-8), monocyte chemoattractant protein (MCP-1), and interleukin-1beta (IL-1beta) in HCT116 cells, and these up-regulations were significantly altered when cells were pre-stimulated with LAB isolated from Korean fermented foods. Poly I-C 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 31278356-6 2019 Kinetic cell viability testing showed that 500 mug/mL of moxifloxacin exposure induced significant decrease (29%) in the viability as early as 1 h. When the inflammatory effects of the antibiotics were examined, a significant induction of IL-8 was observed especially by RVECs after exposure to cefuroxime or vancomycin which was exacerbated by L-alanyl-gamma-D-glutamyl-meso-diaminopimelic acid (Tri-DAP), a NOD1 ligand. L-Ala-gamma-D-Glu-meso-Dap 345-395 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 31278356-6 2019 Kinetic cell viability testing showed that 500 mug/mL of moxifloxacin exposure induced significant decrease (29%) in the viability as early as 1 h. When the inflammatory effects of the antibiotics were examined, a significant induction of IL-8 was observed especially by RVECs after exposure to cefuroxime or vancomycin which was exacerbated by L-alanyl-gamma-D-glutamyl-meso-diaminopimelic acid (Tri-DAP), a NOD1 ligand. tri-dap 397-404 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 31333667-4 2019 PolyI:C increased the expression of interferon-beta (IFN-beta), interleukin-6 (IL-6), interleukin-8 (IL-8), monocyte chemoattractant protein (MCP-1), and interleukin-1beta (IL-1beta) in HCT116 cells, and these up-regulations were significantly altered when cells were pre-stimulated with LAB isolated from Korean fermented foods. Poly I-C 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 31059842-10 2019 Fenofibrate, in presence of IFNgamma plus TNFalpha, dose-dependently inhibited both CXCL10 and CXCL8 release. Fenofibrate 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 31005040-5 2019 The results showed that oridonin significantly inhibited inflammatory mediators PGE2, NO, IL-6, and IL-8 production. oridonin 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 31128992-1 2019 We report a study that seeks to find a correlation between the overall sensitization potential quantified by the expression of IL-8 by stimulated monocytes and the chemical structure of a model contact allergen, 2,4-dinitrochlorobenzene (DNCB). Dinitrochlorobenzene 212-236 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 31128992-1 2019 We report a study that seeks to find a correlation between the overall sensitization potential quantified by the expression of IL-8 by stimulated monocytes and the chemical structure of a model contact allergen, 2,4-dinitrochlorobenzene (DNCB). Dinitrochlorobenzene 238-242 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 31293316-2 2019 18F-Sodium fluoride (18F-NaF) is increasingly used in diagnosing skeletal pain which is not identified on radiographs. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 30203224-4 2019 Both dentifrices contained fluoride in the form of NaF/SiO2. Fluorides 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 30963716-9 2019 Compared to cells treated with oxLDL alone, reactive oxygen species (ROS) generation via nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activation and subsequent activation of p38 mitogen-activated protein kinases followed by nuclear factor kappa B (NF-kappaB) activation and related inflammatory responses including adhesion molecule expression, adhesiveness of monocytic cells, and IL-8 release were also aggravated in cells treated with galectin-3 combined with oxLDL. Reactive Oxygen Species 44-67 C-X-C motif chemokine ligand 8 Homo sapiens 397-401 30963716-9 2019 Compared to cells treated with oxLDL alone, reactive oxygen species (ROS) generation via nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activation and subsequent activation of p38 mitogen-activated protein kinases followed by nuclear factor kappa B (NF-kappaB) activation and related inflammatory responses including adhesion molecule expression, adhesiveness of monocytic cells, and IL-8 release were also aggravated in cells treated with galectin-3 combined with oxLDL. Reactive Oxygen Species 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 397-401 31005040-8 2019 Further studies showed that PPARgamma inhibitor GW9662 could reverse the inhibition of oridonin on PGE2, NO, IL-6, and IL-8 production. 2-chloro-5-nitrobenzanilide 48-54 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 31005040-8 2019 Further studies showed that PPARgamma inhibitor GW9662 could reverse the inhibition of oridonin on PGE2, NO, IL-6, and IL-8 production. oridonin 87-95 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 30895589-11 2019 Apart from a massive airway inflammation indicated by elevated numbers of total cells and neutrophils, the CBA analysis showed increased levels of IL-6 and IL-8 (p < 0.01). cba 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 31326154-9 2019 Among the single plant extracts the Iberis amara extract (IBE) induced high IL-8 releases under non-inflammatory (441 +- 177 pg/ml) and inflammatory (625+- 121 pg/ml) conditions. ibe 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 31326154-16 2019 CONCLUSION: In Het-1A, STW5 inhibited Il-8 releases, although one of its components (IBE) stimulated IL-8 strongly. ibe 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 30903189-4 2019 Nd2O3 exposure initiated an inflammatory response in 16HBE cells via the release of the proinflammatory cytokines interleukin (IL)-6 and IL-8. neodymium oxide 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 30928379-9 2019 Lastly, Treg-secreted high level of IL-8 further induced TGF-beta production from TAMs, and promoted the immunosuppressive tumor microenvironment in MPE. tams 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 31243304-6 2019 Moreover, the attenuated ASC response to TNFalpha priming under smicrog was manifested in decreased production of TNFalpha-dependent pleiotropic cytokines (IL-8 and MCP-1), matrix remodeling proteases, and downregulation of some genes encoding growth factors and cytokines. smicrog 64-71 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 30952010-4 2019 Pretreatment with the DNMT inhibitor 5-Aza-2"-deoxycytidine (5-Aza-CdR) significantly enhanced the expression of the inflammatory cytokines IL-6 and IL-8 in LPS-stimulated hDPCs, indicating that DNA methylation may play a role in hDPC inflammation. Decitabine 37-59 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 30481303-0 2019 Endothelial cells exposed to phosphate and indoxyl sulphate promote vascular calcification through interleukin-8 secretion. Phosphates 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 99-112 30481303-0 2019 Endothelial cells exposed to phosphate and indoxyl sulphate promote vascular calcification through interleukin-8 secretion. Indoxyl sulfate 43-59 C-X-C motif chemokine ligand 8 Homo sapiens 99-112 31084774-1 2019 PET with fluorodeoxyglucose and sodium fluoride (NaF) radiotracers has shown a great promise in assessing patients with multiple myeloma (MM). Sodium Fluoride 32-47 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 31215467-8 2019 RESULTS: The increase of bioactive fluoride in supernatant saliva was higher after application of NaF or AmF compared to fluoridated bioactive glass. Fluorides 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 31242600-5 2019 TNFalpha stimulation led to inducible recruitment of TOP1 to the gene body of IL8, where its inhibition by camptothecin reduced transcription elongation and also led to altered histone H3 acetylation. Camptothecin 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 31212975-11 2019 Taken together, these results provide evidence that quercetin protects ARPE-19 cells from the IL-1beta-stimulated increase in ICAM-1, sICAM-1, IL-6, IL-8 and MCP-1 production by blocking the activation of MAPK and NF-kappaB signaling pathways to ameliorate the inflammatory response. Quercetin 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 31212975-5 2019 The results showed that quercetin could dose-dependently decrease the mRNA and protein levels of ICAM-1, IL-6, IL-8 and monocyte chemoattractant protein-1 (MCP-1). Quercetin 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 31117505-2 2019 All three astaxanthin isomers at 1.2 muM significantly reduced the TNF-alpha-induced secretion of IL-8 by 22-27%. astaxanthine 10-21 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 31212975-9 2019 U0126 and SB202190 could inhibit the expression of IL-6, IL-8 and MCP-1, but SP600125 could not. U 0126 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 31212975-9 2019 U0126 and SB202190 could inhibit the expression of IL-6, IL-8 and MCP-1, but SP600125 could not. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 31212975-10 2019 An NF-kappaB inhibitor (Bay 11-7082) also reduced the expression of ICAM-1, sICAM-1, IL-6, IL-8 and MCP-1. 3-(4-methylphenylsulfonyl)-2-propenenitrile 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 31245395-7 2019 18F-Fluoride (18F-NaF) is an excellent osseous tracer, useful in assessing bone involvement of primary tumors or osseous metastasis. Fluoride ion f-18 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 30865473-6 2019 Moreover, palmitate induced gene expression (monocyte chemoattractant protein 1, matrix metalloproteinase-2, IL-1beta, IL-6, IL-8, and TNF-alpha) and intracellular protein content (plasminogen activator inhibitor-1 and urokinase plasminogen activator) of inflammatory mediators. Palmitates 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 31004595-10 2019 Araloside A concentration-dependently curbed the production of interleukin-6, interleukin-8, prostaglandin E2 and nitric oxide in MH7A cells. araloside A 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 33911592-7 2019 Results: When skin keratinocytes were pre-treated with SAA, it significantly inhibited poly (I:C)-induced expression of inflammatory cytokines including interleukin (IL)-1beta, IL-6, IL-8, tumor necrosis factor-alpha, and CCL20. Poly I-C 87-97 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 31010851-5 2019 Despite possessing an intact N terminus and preserved disulfide bonds, SpyCEP-cleaved CXCL8 had impaired binding to both CXCR1 and CXCR2, pointing to a requirement for the C-terminal alpha-helix. Disulfides 54-63 C-X-C motif chemokine ligand 8 Homo sapiens 86-91 30466341-4 2019 Results: LPS-induced expressions of pro-inflammatory genes IL-6, IL-8, TNF-alpha, IL-1beta, MCP-1, MMP-9, iNOS and COX-2 were significantly and dose-dependently suppressed by XAV939. XAV939 175-181 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 30415310-0 2019 The phosphodiesterase 5 inhibitor sildenafil decreases the proinflammatory chemokine IL-8 in diabetic cardiomyopathy: in vivo and in vitro evidence. Sildenafil Citrate 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 30415310-4 2019 METHODS: IL-8 was quantified: in sera of (30) DCM subjects before (baseline) and after sildenafil (100 mg/day, 3-months) vs. (16) placebo and (15) healthy subjects, by multiplatform array; in supernatants from inflammation-challenged cells after sildenafil (1 microM), by ELISA. Sildenafil Citrate 87-97 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 30415310-6 2019 Sildenafil, not placebo, significantly reduced serum IL-8 (23.7 +- 5.9 pg/ml, p < 0.05 vs. baseline). Sildenafil Citrate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 30415310-8 2019 Sildenafil significantly decreased IL-8 protein release by inflammation-induced Hfaec and PBMC and downregulated IL-8 mRNA in PBMC, without affecting cell number or PDE5 expression. Sildenafil Citrate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 30415310-8 2019 Sildenafil significantly decreased IL-8 protein release by inflammation-induced Hfaec and PBMC and downregulated IL-8 mRNA in PBMC, without affecting cell number or PDE5 expression. Sildenafil Citrate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 30415310-9 2019 CONCLUSION: Sildenafil might be suggested as potential novel pharmacological tool to control DCM progression through IL-8 targeting at systemic and cellular level. Sildenafil Citrate 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 30478740-9 2019 Remarkable, after 6 h CdCl2-treatment, a relevant increase in TNF-alpha, IL-6 and IL-8 mRNA was observed and this effect was blocked by the presence of an ERbeta-selective antagonist. Cadmium Chloride 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 31101589-6 2019 Rifamycin also antagonized TNFalpha and LPS-induced NFkappaB activities and inhibited IL1beta-induced synthesis of inflammatory chemokine, IL8. rifamycin SV 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 31101589-8 2019 Thus, rifamycin exhibits potent anti-inflammatory activities, characterized by in vitro PXR activation and concomitant CYP3A4 and PgP induction, in parallel with potent NFkappaB inhibition and concomitant IL8 inhibition. rifamycin SV 6-15 C-X-C motif chemokine ligand 8 Homo sapiens 205-208 30888047-6 2019 In human cells, while Cr induced a release of ATP, IL-6, and IL-8 from BEAS-2B cells, whole blood cells, such as eosinophils, and CD4+ T cells, P2 x 7 receptor inhibitor (A740003) reduced such effects, as denoted by reduced levels of ATP, IL-6, and IL-8. Creatine 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 30888047-6 2019 In human cells, while Cr induced a release of ATP, IL-6, and IL-8 from BEAS-2B cells, whole blood cells, such as eosinophils, and CD4+ T cells, P2 x 7 receptor inhibitor (A740003) reduced such effects, as denoted by reduced levels of ATP, IL-6, and IL-8. Creatine 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 249-253 31183190-3 2019 Levocetirizine is a second generation H1 antihistamine with anti-inflammatory and IL-8 suppression properties. levocetirizine 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 31010851-6 2019 SpyCEP-cleaved CXCL8 had similarly impaired binding to the glycosaminoglycan heparin. glycosaminoglycan heparin 59-84 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 31010851-7 2019 Enzymatic removal of neutrophil glycosaminoglycans was observed to ablate neutrophil navigation of a CXCL8 gradient, whereas navigation of an fMLF gradient remained largely intact. Glycosaminoglycans 32-50 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 31002348-0 2019 Acquisition of gemcitabine resistance enhances angiogenesis via upregulation of IL-8 production in pancreatic cancer. gemcitabine 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30688757-1 2019 BACKGROUND: Fluorine-18-labeled sodium fluoride (F-NaF) uptake measured with PET in the vessel walls can indicate active microcalcification, a potential biomarker of higher-risk plaques, which are not indicated by macrocalcification measured with computed tomography (CT). Fluorine-18 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 30688757-1 2019 BACKGROUND: Fluorine-18-labeled sodium fluoride (F-NaF) uptake measured with PET in the vessel walls can indicate active microcalcification, a potential biomarker of higher-risk plaques, which are not indicated by macrocalcification measured with computed tomography (CT). Sodium Fluoride 32-47 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 30688757-2 2019 The aim of this study was to determine the extent to which F-NaF uptake is correlated with calcification at arterial plaques in cancer patients undergoing whole-body PET/CT imaging. Fluorine 59-60 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 30688757-7 2019 We found a weak but statistically significant positive correlation between CS and F-NaF uptake. Cesium 75-77 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 31028903-5 2019 Exposure of these cells to lipogenic (insulin, glucose, fatty acids) and pro-inflammatory factors (IL-1beta, TNF-alpha, TGF-beta) resulted in a characteristic NASH response, as indicated by intracellular lipid accumulation, modulation of NASH-specific gene expression, increased caspase-3/7 activity and the expression and/or secretion of inflammatory markers, including CCL2, CCL5, CCL7, CCL8, CXCL5, CXCL8, IL1a, IL6 and IL11. Fatty Acids 56-67 C-X-C motif chemokine ligand 8 Homo sapiens 402-407 31245005-9 2019 For example, women who had elevated DGLA (highest quartile) were twice as (adjusted OR 2.06, 95% CI 1.42 to 2.98) likely to have higher interleukin (IL)-8 (p<0.0001) levels. 8,11,14-Eicosatrienoic Acid 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 136-154 31292053-4 2019 Reverse transcription PCR was used to test the effect of U0126 at different concentrations (0, 1, 5, 10 mumol/L) on the mRNA expression of IL-8 induced by Stattic in THP-1 cells. U 0126 57-62 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 31292053-9 2019 In addition, U0126, a selective inhibitor of ERK pathway, inhibited Stattic-induced IL-8 expression in a concentration-dependent manner. U 0126 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 31070650-6 2019 Furthermore, TPA obviously assuaged TNF-alpha-evoked up-regulation of IL-8 and IL-6 expression, down-regulation of occludin and ZO-3 expression, and markedly suppressed the activation and protein expression of NF-kappaB p65. Tetradecanoylphorbol Acetate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 31231362-9 2019 C-SVMP was able to induce increased production of the cytokines IL-1beta and IL-6 and the chemokines CXCL8/IL-8, CCL2/MCP-1, and CXCL9/MIG in the human whole blood model. c-svmp 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 31231362-9 2019 C-SVMP was able to induce increased production of the cytokines IL-1beta and IL-6 and the chemokines CXCL8/IL-8, CCL2/MCP-1, and CXCL9/MIG in the human whole blood model. c-svmp 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 31231362-10 2019 The addition of compstatin to the reactions caused a significant reduction in the production of IL-1beta, CXCL8/IL-8, and CCL2/MCP-1 in cells treated with C-SVMP. c-svmp 155-161 C-X-C motif chemokine ligand 8 Homo sapiens 106-111 31113462-9 2019 CuO NMs and CuSO4 stimulated an increase in IL-8 secretion, which was greatest in the Caco-2/HT29-MTX co-culture model. cupric oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 31113462-9 2019 CuO NMs and CuSO4 stimulated an increase in IL-8 secretion, which was greatest in the Caco-2/HT29-MTX co-culture model. Copper Sulfate 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 31113462-9 2019 CuO NMs and CuSO4 stimulated an increase in IL-8 secretion, which was greatest in the Caco-2/HT29-MTX co-culture model. Methotrexate 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 30851105-4 2019 First, we demonstrated that levels of Cinc-1, the rat homolog of IL-8, are increased in the lung fluid and tissue compartment in a rat model of DA-induced BO. amsonic acid 144-146 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 30851105-6 2019 We then tested the hypothesis that DA-induced epithelial IL-8 protein occurs in an epidermal growth factor receptor (EGFR)-dependent manner. amsonic acid 35-37 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 30851105-7 2019 In these in vitro experiments we demonstrated that epithelial IL-8 protein is blocked by the EGFR tyrosine kinase inhibitor AG1478 and by inhibition of tumor necrosis factor-alpha converting enzyme using the small molecule inhibitor, TAPI-1. RTKI cpd 124-130 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 30851105-8 2019 Finally, we demonstrated that DA-induced IL-8 is dependent upon ERK1/2 and Mitogen activated protein kinase kinase activation downstream of EGFR signaling using the small molecule inhibitors AG1478 and PD98059. amsonic acid 30-32 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 30851105-8 2019 Finally, we demonstrated that DA-induced IL-8 is dependent upon ERK1/2 and Mitogen activated protein kinase kinase activation downstream of EGFR signaling using the small molecule inhibitors AG1478 and PD98059. RTKI cpd 191-197 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 30851105-8 2019 Finally, we demonstrated that DA-induced IL-8 is dependent upon ERK1/2 and Mitogen activated protein kinase kinase activation downstream of EGFR signaling using the small molecule inhibitors AG1478 and PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 202-209 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 31130634-5 2019 The results showed that Phlor (10-50 muM) decreased the synthesis of PGE2 and IL-8 and the formation of AGEs by different mechanisms. Phloretin 24-29 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 31245005-10 2019 Conversely, women with high palmitoleic, oleic, and linolenic acid levels had reduced odds (>=2-fold, p<0.01 to p<0.001) for having higher IL-8, IL-6 or tumor necrosis factor-alpha levels. oleic 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 31245005-10 2019 Conversely, women with high palmitoleic, oleic, and linolenic acid levels had reduced odds (>=2-fold, p<0.01 to p<0.001) for having higher IL-8, IL-6 or tumor necrosis factor-alpha levels. alpha-Linolenic Acid 52-66 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 31139184-3 2019 Pretreatment of human RASFs with JWH-015 (10-20 muM) markedly inhibited the ability of pro-inflammatory cytokine interleukin-1beta (IL-1beta) to induce production of IL-6 and IL-8 and cellular expression of inflammatory cyclooxygenase-2 (COX-2). JHW 015 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 30996116-6 2019 DOX influenced inflammatory responses by inducing a significant increase in the expression of pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha) and cyclooxigenase-2 (COX-2), of inflammatory interleukins (IL), such as interleukin-6 (IL-6) and interleukin-8 (IL-8), and the inflammatory proteins mediators metalloproteinase-2 and metalloproteinase-9 (MMP2 and MMP9). Doxorubicin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 268-281 30996116-6 2019 DOX influenced inflammatory responses by inducing a significant increase in the expression of pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha) and cyclooxigenase-2 (COX-2), of inflammatory interleukins (IL), such as interleukin-6 (IL-6) and interleukin-8 (IL-8), and the inflammatory proteins mediators metalloproteinase-2 and metalloproteinase-9 (MMP2 and MMP9). Doxorubicin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 283-287 30996116-7 2019 IL-8 secretion in the culture supernatants and MMP9 activity also significantly raised after DOX treatment. Doxorubicin 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 31105936-2 2019 Uptake of 18F-sodium fluoride (18F-NaF) in the aortic wall reflects metabolically active areas of calcification. 18f-sodium fluoride 10-29 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 31053727-7 2019 Furthermore, transfected chondrocytes with miR-125b mimic in the presence of IL-1beta also showed marked inhibition in the secretion of several proinflammatory cytokines, chemokines and growth factors including IL-6, IL-8, INF-gamma, TGF-beta1, IGFBP-1 and PGDF-BB. mir-125b 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 31105936-11 2019 Conclusion: In a cohort of postmenopausal women, 18F-NaF uptake as measured by TBR in the lumbar aorta did not predict progression of aortic calcification as detected by computed tomography over a four-year follow-up. tbr 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 29232287-7 2019 Similar effects on IL-1beta, IL-6, and IL-8 levels were observed when cells were treated with simvastatin, pravastatin, and the renin-angiotensin system inhibitors spironolactone, captopril, lisinopril, candesartan, and losartan. Simvastatin 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 31052583-8 2019 NM-200 induced production of IL-8, a potent attractor and activator of neutrophils, growth factors (VEGF and IGF-1) and superoxide. nm-200 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 31052583-8 2019 NM-200 induced production of IL-8, a potent attractor and activator of neutrophils, growth factors (VEGF and IGF-1) and superoxide. Superoxides 120-130 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 29232287-7 2019 Similar effects on IL-1beta, IL-6, and IL-8 levels were observed when cells were treated with simvastatin, pravastatin, and the renin-angiotensin system inhibitors spironolactone, captopril, lisinopril, candesartan, and losartan. Pravastatin 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 30648905-5 2019 In both cell types, challenge with arachidonic acid (AA) (omega-6 PUFA) and poly(I:C) or LTA led to substantially greater IL-6 and CXCL8 release than either challenge alone, demonstrating synergy. Arachidonic Acid 35-51 C-X-C motif chemokine ligand 8 Homo sapiens 131-136 30726114-5 2019 Meanwhile, fMLF or IL-8 stimulation yields the longer terminating time than that on PMA stimulation but results in a similar shedding extent for PMNs. Tetradecanoylphorbol Acetate 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 30648905-5 2019 In both cell types, challenge with arachidonic acid (AA) (omega-6 PUFA) and poly(I:C) or LTA led to substantially greater IL-6 and CXCL8 release than either challenge alone, demonstrating synergy. omega-6 pufa 58-70 C-X-C motif chemokine ligand 8 Homo sapiens 131-136 30851246-3 2019 When tested in vitro on human dendritic cells (DCs), CHF6001 decreased the release of pro-inflammatory cytokines (TNF-alpha and IL-6), chemokines (CXCL8, CCL3, CXCL10 and CCL19) and of Th1- and Th17-polarizing cytokines (IL-12, IL-23 and IL-1beta). 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(cyclopropylmethoxy)-4-(methylsulfonamido)benzoyloxy)ethyl)pyridine 1-oxide 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 147-152 30846359-0 2019 Decitabine improves platelet recovery by down-regulating IL-8 level in MDS/AML patients with thrombocytopenia. Decitabine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 30922967-5 2019 However, the intracellular superoxide, Zn ions, or release of interleukin-8 after ZnO NP exposure were not significantly affected by the presence of CC. zno np 82-88 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 30888996-1 2019 PURPOSE: [F]-sodium fluoride ([F]NaF) is a well-established bone-seeking agent that has shown promise to assess bone turnover in a variety of disorders, but its distribution in healthy knee joints has not been explored. Sodium Fluoride 13-28 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 30884698-7 2019 Storage of TiO2 nanoparticles inside the cells affected enterocytes viability and triggered the production of pro-inflammatory cytokines, including TNF-alpha and IL-8. titanium dioxide 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 30306335-11 2019 However, only NaF-gel2 and NaF-TP induced remineralization. neotetrazolium 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 30867226-0 2019 Role of Protein Tyrosine Phosphatase Epsilon (PTPepsilon) in Leukotriene D4-Induced CXCL8 Expression. Leukotriene D4 61-75 C-X-C motif chemokine ligand 8 Homo sapiens 84-89 31934009-5 2019 Pearson correlation analysis showed that the serum 25(OH)D level in patients with T2DM had a negative correlation with HOMA-IR (r=-0.750, P<0.001), TNF-alpha (r=-0.705, P<0.001), IL-1beta (r=-0.661, P<0.001), IL-8 (r=-0.645, P<0.001), and IL-6 (r=-0.609, P<0.001). 25-hydroxyvitamin D3-bromoacetate 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 31005721-8 2019 EGCG treatment reduced CSM-induced inflammatory chemokine interleukin (IL)-8 productions in the supernatant via the inhibition of ERK1/2, p38 MAPK and NF-kappaB pathways. epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 58-76 30535530-5 2019 More importantly, treatment of HepG2 cells with rAGAP downregulated protein expression of HIF-1alpha, suppressed activities of HIF, reduced secretion of VEGF and IL-8, and suppressed HepG2-induced tube formation by HUVEC, which was reversed by co-incubation with SC-79 (an AKT activator). ragap 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 30426301-6 2019 Treatment of the senescent hHSCs with ERK1/2 inhibitor, SCH772984, significantly decreased the levels of angiopoietin like 4 (ANGPTL4), C-C motif chemokine ligand 7 (CCL7), Interleukin-8 (IL-8), platelet factor 4 variant 1 (PF4V1), and TNF superfamily member 15 (TNFSF15) mRNA levels in a dose-dependent manner. SCH772984 56-65 C-X-C motif chemokine ligand 8 Homo sapiens 173-186 30426301-6 2019 Treatment of the senescent hHSCs with ERK1/2 inhibitor, SCH772984, significantly decreased the levels of angiopoietin like 4 (ANGPTL4), C-C motif chemokine ligand 7 (CCL7), Interleukin-8 (IL-8), platelet factor 4 variant 1 (PF4V1), and TNF superfamily member 15 (TNFSF15) mRNA levels in a dose-dependent manner. SCH772984 56-65 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 30461332-6 2019 Moreover, only co-exposure to ZnO NPs and SA significantly promoted the release of interleukin-8. Zinc Oxide 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 30248704-0 2019 Serine Protease Mauritanicain from Euphorbia mauritanica and Phorbol-12-myristate-13-acetate Modulate the IL-8 Release in Fibroblasts and HaCaT Keratinocytes. Tetradecanoylphorbol Acetate 61-92 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 30248704-7 2019 The results indicated that the combination of the protease mauritanicain from Euphorbia mauritanica and phorbol-12-myristate-13-acetate induced a significantly increased IL-8 release in HaCaT keratinocytes compared to single treatments. Tetradecanoylphorbol Acetate 104-135 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 30461332-6 2019 Moreover, only co-exposure to ZnO NPs and SA significantly promoted the release of interleukin-8. stearic acid 42-44 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 31110480-8 2019 Results: In the present study, RIPC treatment significantly reduced plasma levels of cardiac troponin T (p < 0.05), heart-type fatty acid binding protein (p < 0.05), ischemia modified albumin (p < 0.05), malondialdehyde (p < 0.05), as well as plasma levels of pro-inflammatory cytokines including IL-6, IL-8, and TNF-alpha (P < 0.05, respectively). ripc 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 315-319 31101174-14 2019 The rejection group maintained higher levels of IL-8 for 11 days (range: 7-30) compared to the SGF group (P = .002) and the IL-8 levels correlated with serum creatinine levels (r = 0.621, P = .001). Creatinine 158-168 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 31044584-4 2019 Furthermore, by potentially up-regulating A2A and A3 adenosine receptors, EMF increases cAMP accumulation from astrocytes and reduces the expression of inflammatory cytokines TNF alpha and IL-8, thus initiating neurorestoration. Adenosine 53-62 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 30753461-5 2019 We further showed that treatment with FK506 (tacrolimus) possibly inhibits the increase in IL-8 levels in RA patients with anti-RANKL Ab, and in vitro assay confirmed that FK506 suppressed IL-8 production in pre-OCLs. Tacrolimus 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 30753461-5 2019 We further showed that treatment with FK506 (tacrolimus) possibly inhibits the increase in IL-8 levels in RA patients with anti-RANKL Ab, and in vitro assay confirmed that FK506 suppressed IL-8 production in pre-OCLs. Tacrolimus 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 30753461-5 2019 We further showed that treatment with FK506 (tacrolimus) possibly inhibits the increase in IL-8 levels in RA patients with anti-RANKL Ab, and in vitro assay confirmed that FK506 suppressed IL-8 production in pre-OCLs. Tacrolimus 45-55 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 30753461-5 2019 We further showed that treatment with FK506 (tacrolimus) possibly inhibits the increase in IL-8 levels in RA patients with anti-RANKL Ab, and in vitro assay confirmed that FK506 suppressed IL-8 production in pre-OCLs. Tacrolimus 45-55 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 30753461-5 2019 We further showed that treatment with FK506 (tacrolimus) possibly inhibits the increase in IL-8 levels in RA patients with anti-RANKL Ab, and in vitro assay confirmed that FK506 suppressed IL-8 production in pre-OCLs. Tacrolimus 172-177 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 30753461-5 2019 We further showed that treatment with FK506 (tacrolimus) possibly inhibits the increase in IL-8 levels in RA patients with anti-RANKL Ab, and in vitro assay confirmed that FK506 suppressed IL-8 production in pre-OCLs. Tacrolimus 172-177 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 31008484-6 2019 EP1/EP3 agonist 17-phenyl-trinor-PGE2 stimulated IL-6 and TNFalpha whilst suppressing IL-1beta and CXCL8 output. 17-phenyltrinorprostaglandin E2 16-37 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 31008484-5 2019 The results showed that, PGE2 increased interleukin 6 (IL-6) and tumor necrosis factor alpha (TNFalpha) output, decreased chemokine (c-x-c motif) ligand 8 (CXCL8) output in a dose-dependent manner, but had no effect on IL-1beta and chemokine (c-c motif) ligand 2 (CCL-2) secretion of HUSMCs. Dinoprostone 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 156-161 31008484-7 2019 The effects of 17-phenyl-trinor-PGE2 on IL-1beta and CXCL8 secretion were remained whereas its effect on IL-6 and TNFalpha output did not occur in the cells with EP3 knockdown. 17-phenyltrinorprostaglandin E2 15-36 C-X-C motif chemokine ligand 8 Homo sapiens 53-58 31017900-9 2019 ML2044-stimulated IL-4 and CXCL8/IL-8 achieved the highest sensitivity (85.71% and 100%) and the highest specificity (95.24% and 84.21%) for discriminating PB patients from HHCs and TB patients, respectively. pladienolide B 156-158 C-X-C motif chemokine ligand 8 Homo sapiens 27-32 31105691-5 2019 DAPT also inhibited the contact-dependent induction of CXCL8, but not of CCL5, in TNFalpha- and IL-1beta-stimulated TNBC:MSC/CAF co-cultures; some level of heterogeneity between the responses of different TNBC cell lines was noted, with MDA-MB-231:MSC/CAF co-cultures being the most sensitive to DAPT. dapt 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 55-60 31017900-9 2019 ML2044-stimulated IL-4 and CXCL8/IL-8 achieved the highest sensitivity (85.71% and 100%) and the highest specificity (95.24% and 84.21%) for discriminating PB patients from HHCs and TB patients, respectively. pladienolide B 156-158 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 31105821-6 2019 Notably, our findings indicate that sitagliptin possesses an anti-inflammatory effect against H/R-induced expression of IL-6, IL-8, and TNF-alpha as well as secretion of HMGB1. Sitagliptin Phosphate 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 30084946-0 2019 Chronic Resveratrol Treatment Reduces the Pro-angiogenic Effect of Human Fibroblast "Senescent-Associated Secretory Phenotype" on Endothelial Colony-Forming Cells: The Role of IL8. Resveratrol 8-19 C-X-C motif chemokine ligand 8 Homo sapiens 176-179 30084946-6 2019 IL8-subtraction mitigated the pro-angiogenic features of CM sen and the associated intracellular signaling in ECFCs, indicating a prominent role of IL8 in the pro-angiogenic effects of CM sen. cm sen 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 30084946-6 2019 IL8-subtraction mitigated the pro-angiogenic features of CM sen and the associated intracellular signaling in ECFCs, indicating a prominent role of IL8 in the pro-angiogenic effects of CM sen. cm sen 185-191 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 30084946-6 2019 IL8-subtraction mitigated the pro-angiogenic features of CM sen and the associated intracellular signaling in ECFCs, indicating a prominent role of IL8 in the pro-angiogenic effects of CM sen. cm sen 185-191 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 30084946-7 2019 IL8 modulation is an important mechanism underlying the antiangiogenic activity of resveratrol on MRC5 SASP. Resveratrol 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 30797108-1 2019 In the present work, for the first time we takes the advantages of chitosan-Nafion (Chit-Naf) composite as a highly conductive surface platform and a novel CNT-based signal amplification strategy to develop a lable-free impedimetricaptamer-based sensor for highly sensitive detection of As(III). as(iii) 287-294 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 30797108-2 2019 The electrochemical impedance spectroscopy (EIS) investigations surprisingly revealed that the glassy carbon electrode (GC) electrode modified with Chit-Naf composite had higher electron transfer kinetics compared the bare GC, GC/Naf and GC/Chit electrodes, which promises a great potential as an efficient platform in construction of biosensing assays. Carbon 102-108 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 30797108-2 2019 The electrochemical impedance spectroscopy (EIS) investigations surprisingly revealed that the glassy carbon electrode (GC) electrode modified with Chit-Naf composite had higher electron transfer kinetics compared the bare GC, GC/Naf and GC/Chit electrodes, which promises a great potential as an efficient platform in construction of biosensing assays. Carbon 102-108 C-X-C motif chemokine ligand 8 Homo sapiens 230-233 31010106-11 2019 The levels of IL-8, C reactive protein (CRP), and cyclooxygenase (COX)-2 increased only after exposure to I-PM2.5. i-pm2 106-111 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 31015845-11 2019 Conclusion: We speculate that in young children with sleep-related CIH, an enhanced production capacity of IL-8 precedes the development of systemic inflammatory markers. cih 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 31105821-6 2019 Notably, our findings indicate that sitagliptin possesses an anti-inflammatory effect against H/R-induced expression of IL-6, IL-8, and TNF-alpha as well as secretion of HMGB1. r 96-97 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 30969964-6 2019 Mutations of the CXCL8-UTR-reporter revealed that cell type-specific expression required: 1) a 3" UTR of at least three hundred bases; and 2) an AU base content that exceeds fifty percent in the first hundred bases of the 3" UTR immediately after the stop codon, which we dub AU-rich proximal UTR sequences (APS). Gold 145-147 C-X-C motif chemokine ligand 8 Homo sapiens 17-22 30796179-9 2019 Q0bolton-AAT bound IL-8 and leukotriene B4, comparable to healthy control M-AAT, and significantly decreased leukotriene B4-induced neutrophil adhesion (p = 0.04). q0bolton-aat 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 30664962-10 2019 Pyrazinib (P3) significantly reduced the secretions of IL-6 (p = 0.0006), IL-8 (p = 0.0488), and IL-4 (p = 0.0111) in OE33R cells. SCHEMBL9791651 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 30836753-5 2019 Moreover, the adsorption property with respect to Cd2+ and Ni2+ in wastewater has been largely effected by the pH and was less influenced by the ionic strength and humic acid, and the GCP1:2:4 hydrogel possessed excellent adsorptive and recyclable properties. Nickel(2+) 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 30972350-6 2019 The effect of LPNs on lipopolysaccharide (LPS)-induced IL-8 production from human NuLi-1 BECs was tested by ELISA. lpns 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 30972350-10 2019 Nebulised miR-17-loaded LPNs downregulated LPS-induced IL-8 secretion by >40% in BECs. lpns 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 30860845-0 2019 Quantum Dynamics Calculations of Na (32S, 32P) + HF NaF + H Reactions. 32S 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 30860845-0 2019 Quantum Dynamics Calculations of Na (32S, 32P) + HF NaF + H Reactions. Phosphorus-32 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 30860845-6 2019 For the Na(3P) + HF scattering, which can lead to the formation of either the ground state NaF + H product or Na(3S) + HF reactant via the harpooning process, the calculated result for the integral cross section shows excellent agreement with the available experimental result indicating the reasonable accuracy of the interstate coupling term of the employed PES. na(3p) 8-14 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 30860845-6 2019 For the Na(3P) + HF scattering, which can lead to the formation of either the ground state NaF + H product or Na(3S) + HF reactant via the harpooning process, the calculated result for the integral cross section shows excellent agreement with the available experimental result indicating the reasonable accuracy of the interstate coupling term of the employed PES. na(3s) 110-116 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 30864448-0 2019 Structural Origins of RF3/NaRF4 Nanocrystal Precipitation from Phase-Separated SiO2-Al2O3-RF3-NaF Glasses: A Molecular Dynamics Simulation Study. 1-(thiophen-2-ylacetyl)-4-(3-thiophen-2-yl-1,2,4-oxadiazol-5-yl)piperidine 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 31041358-10 2019 Interleukin-8 levels increased in nasal samples (using synthetic absorptive matrix strips) and decreased serum neutrophil-elastase-mediated degradation of elastin decreased in danirixin-treated participants, suggesting effective target engagement. danirixin 176-185 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 30864448-0 2019 Structural Origins of RF3/NaRF4 Nanocrystal Precipitation from Phase-Separated SiO2-Al2O3-RF3-NaF Glasses: A Molecular Dynamics Simulation Study. narf4 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 30864448-4 2019 These fluoride-enriched regions can serve as the precursor for RF3, cubic and hexagonal NaRF4, and NaF crystal precipitation. Fluorides 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 30864448-5 2019 The results also confirm that the concentration of Na+ in the fluoride phase plays a key role in determining the crystal phases (RF3, NaRF4, or NaF) and crystal structure (cubic vs hexagonal NaRF4) to be precipitated. Fluorides 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 144-147 30836753-6 2019 These results demonstrated that the GCP1:2:4 hydrogel could serve as a desirable adsorbent to get rid of heavy metal ions in sewage. Metals 111-116 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 30846336-1 2019 BACKGROUND: Fluorine-18 sodium fluoride (NaF), a bone-seeking radiopharmaceutical used to detect osseous metastases, localizes in regions of microcalcification in atherosclerosis. fluorine-18 sodium fluoride 12-39 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 29931577-4 2019 The results showed that sodium fluoride (NaF) induced deacetylation and decreased expression of the p16 gene via inhibition of specificity protein 1 (Sp1) binding to its response element, which accounts for NaF increasing cell viability and promoting proliferation in human primary osteoblasts. Sodium Fluoride 24-39 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 30652495-12 2019 The antioxidant N-acetylcysteine prevents CSE-induced miR-29b downregulation and BRD4 and IL-8 upregulation. Acetylcysteine 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 29931577-4 2019 The results showed that sodium fluoride (NaF) induced deacetylation and decreased expression of the p16 gene via inhibition of specificity protein 1 (Sp1) binding to its response element, which accounts for NaF increasing cell viability and promoting proliferation in human primary osteoblasts. Sodium Fluoride 24-39 C-X-C motif chemokine ligand 8 Homo sapiens 207-210 30660785-7 2019 RESULTS: Bacterial biomass, neutrophil percentage, IL-8, and IL-1beta levels were significantly higher in children with PBB compared with control patients. pbb 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 31025289-10 2019 A significant increase in CXCL8 and FGF-2 expression was observed with HPAF-CD11/CAFs co-culture and to a lower extent with HPAF/CAFs co-culture. hpaf-cd11 71-80 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 31025289-10 2019 A significant increase in CXCL8 and FGF-2 expression was observed with HPAF-CD11/CAFs co-culture and to a lower extent with HPAF/CAFs co-culture. hpaf 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 30548842-5 2019 The affinity of the resulting tetramethylrhodamine-labeled macrocyclic peptomers to CXCL8 is increased by at least 1 order of magnitude compared to the original linear sequences. tetramethylrhodamine 30-50 C-X-C motif chemokine ligand 8 Homo sapiens 84-89 30585832-9 2019 In contrast, acetylsalicylic acid treatment resulted in enhanced plasma levels of tumor necrosis factor-alpha (+53%; p = 0.02), interleukin-6 (+91%; p = 0.03), and interleukin-8 (+42%; p = 0.02) upon the second challenge, whereas plasma levels of the key antiinflammatory cytokine interleukin-10 were attenuated (-40%; p = 0.003). Aspirin 13-33 C-X-C motif chemokine ligand 8 Homo sapiens 164-177 30906451-10 2019 Puerarin preconditioning can reduce the NF-kappaB activation and the overexpression of IL-6 and IL-8 in neutrophils, and it inhibits the release of myocardial enzyme cTnI and CK-MB reflecting myocardial cell protection. puerarin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 30823334-11 2019 Interleukin 8 was inversely associated with PFOS and PFNA. perfluorooctane sulfonic acid 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 30341641-5 2019 Hybrid imaging with bone-seeking tracers such as SPECT/CT with 99mTc-labelled bisphosphonates or PET/CT with 18F-labelled sodium fluoride (18F-NaF) combines high radionuclide uptake with morphological details and provides accurate diagnosis of osteoid osteoma and additional information for treatment planning. Sodium Fluoride 122-137 C-X-C motif chemokine ligand 8 Homo sapiens 143-146 30935522-6 2019 DISCUSSION: GTP play a role in reducing TNF-alpha, Interleukin 1beta (IL-1beta), IL-6, IL-8, and 17; downregulate cyclooxygenase-mediated I kappa B kinase and transcription of NFkappaB. Guanosine Triphosphate 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 30623574-2 2019 Proinflammatory cytokines IL-6 and IL-8 are related to steroid-insensitive asthma. Steroids 55-62 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 30623574-7 2019 Both Erlotinib (Tarceva) and Osimertinib (AZD-9291) reduced the levels of HDM-stimulated IL-6 and IL-8 levels in BEAS-2B cells. Erlotinib Hydrochloride 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 30623574-7 2019 Both Erlotinib (Tarceva) and Osimertinib (AZD-9291) reduced the levels of HDM-stimulated IL-6 and IL-8 levels in BEAS-2B cells. Erlotinib Hydrochloride 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 30623574-7 2019 Both Erlotinib (Tarceva) and Osimertinib (AZD-9291) reduced the levels of HDM-stimulated IL-6 and IL-8 levels in BEAS-2B cells. osimertinib 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 30623574-7 2019 Both Erlotinib (Tarceva) and Osimertinib (AZD-9291) reduced the levels of HDM-stimulated IL-6 and IL-8 levels in BEAS-2B cells. osimertinib 42-50 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 30623574-10 2019 Our findings highlight EGFR-TKIs, Tarceva, and AZD-9291, attenuate HDM-induced inflammatory IL-6 and IL-8 cytokines via EGFR signaling axis pathway, but not AMPK signaling pathway. Erlotinib Hydrochloride 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 30623574-10 2019 Our findings highlight EGFR-TKIs, Tarceva, and AZD-9291, attenuate HDM-induced inflammatory IL-6 and IL-8 cytokines via EGFR signaling axis pathway, but not AMPK signaling pathway. osimertinib 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 30906451-7 2019 The positive rates of NF-kappaB, IL-6 and IL-8 at different time-points were lower in patients of the puerarin group than in those of the control group (and the differences at T3 were statistically significant). puerarin 102-110 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 30739130-7 2019 Biomarker profiling indicated potential modest effects of toreforant on gene expression of histamine-1-receptor, tumor necrosis factor-alpha, and interleukin-8 in synovium. Toreforant 58-68 C-X-C motif chemokine ligand 8 Homo sapiens 146-159 30592634-5 2019 To elucidate the function of paracrine CXCL8 in AML, we blocked CXCL8 binding to the C-X-C motif chemokine receptor (CXCR)2 in the AML cells using SB225002. SB 225002 147-155 C-X-C motif chemokine ligand 8 Homo sapiens 64-69 30295316-16 2019 Vitamin D inhibited IL-6 and IL-8 production stimulated by G-HSA or HSA + IL-1beta or IL-1beta + IL-17. g-hsa 59-64 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 29524030-5 2019 The vitreous IL-8 level of DME patients with subretinal fluid was significantly higher than both control (p = 0.002) and DME without subretinal fluid groups (p = 0.019). dme 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 29524030-5 2019 The vitreous IL-8 level of DME patients with subretinal fluid was significantly higher than both control (p = 0.002) and DME without subretinal fluid groups (p = 0.019). dme 121-124 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 29524030-8 2019 CONCLUSIONS: IL-8 level in vitreous samples was higher in DME patients with subretinal fluid than those without subretinal fluid, suggesting that inflammation is an important factor in the progression of DME leading to the subretinal fluid formation in diabetic patients. dme 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 29524030-8 2019 CONCLUSIONS: IL-8 level in vitreous samples was higher in DME patients with subretinal fluid than those without subretinal fluid, suggesting that inflammation is an important factor in the progression of DME leading to the subretinal fluid formation in diabetic patients. dme 204-207 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 31010609-10 2019 Dexamethasone, but not maxacalcitol nor the phosphodiesterase 4 inhibitor apremilast, partially inhibited the CXCL8 and CCL20 secretion. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 110-115 30213848-1 2019 Coronary 18F-sodium fluoride (18F-NaF) PET identifies ruptured plaques in patients with recent myocardial infarction and localizes to atherosclerotic lesions with active calcification. 18f-sodium fluoride 9-28 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 30295316-13 2019 G-HSA or HSA when combined with IL-1beta or IL-1beta + IL-17 synergistically stimulated IL-6 and IL-8. g-hsa 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 30295316-16 2019 Vitamin D inhibited IL-6 and IL-8 production stimulated by G-HSA or HSA + IL-1beta or IL-1beta + IL-17. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 30726064-5 2019 The CXCL8-Arg6His analogue stimulated calcium release, phosphorylation of ERK1/2, and chemotaxis in cells expressing CXCR1. Calcium 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 4-9 30794923-11 2019 Ibuprofen-acyl glucuronide, but not ibuprofen, inhibited the release of IL-8 evoked by AITC from cultured bronchial epithelial cells. Ibuprofen 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 30794923-11 2019 Ibuprofen-acyl glucuronide, but not ibuprofen, inhibited the release of IL-8 evoked by AITC from cultured bronchial epithelial cells. acyl glucuronide 10-26 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 30769285-8 2019 The mechanical study revealed that tumoral NOX4-induced reactive oxygen species (ROS) stimulated various cytokine production, including CCL7, IL8, CSF-1 and VEGF-C, via PI3K/Akt signaling-dependent manner. Reactive Oxygen Species 56-79 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 30769285-8 2019 The mechanical study revealed that tumoral NOX4-induced reactive oxygen species (ROS) stimulated various cytokine production, including CCL7, IL8, CSF-1 and VEGF-C, via PI3K/Akt signaling-dependent manner. Reactive Oxygen Species 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 30677406-2 2019 HAT enhanced release of interleukin-8 (IL-8) from HBECs at 10-100 mU/mL and the enhanced release was almost completely abolished by 50 muM leupeptin, a serine protease inhibitor. leupeptin 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 30677406-2 2019 HAT enhanced release of interleukin-8 (IL-8) from HBECs at 10-100 mU/mL and the enhanced release was almost completely abolished by 50 muM leupeptin, a serine protease inhibitor. leupeptin 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 30677406-2 2019 HAT enhanced release of interleukin-8 (IL-8) from HBECs at 10-100 mU/mL and the enhanced release was almost completely abolished by 50 muM leupeptin, a serine protease inhibitor. Serine 152-158 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 30677406-2 2019 HAT enhanced release of interleukin-8 (IL-8) from HBECs at 10-100 mU/mL and the enhanced release was almost completely abolished by 50 muM leupeptin, a serine protease inhibitor. Serine 152-158 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 30409612-4 2019 When lycopene was paired with the methoxylated anthocyanins, the anti-inflammatory effect on the inhibition of the cytokine IL-8, which is a pro-inflammatory biomarker, was increased by 15-69% of the expected additive activity, indicating synergistic interaction between the compounds. Lycopene 5-13 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 30409612-4 2019 When lycopene was paired with the methoxylated anthocyanins, the anti-inflammatory effect on the inhibition of the cytokine IL-8, which is a pro-inflammatory biomarker, was increased by 15-69% of the expected additive activity, indicating synergistic interaction between the compounds. Anthocyanins 47-59 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 30716336-7 2019 Our study proved that exosomes arising from KG1A cells could propel BMSCs to generate IL-8, which could regulate the effect of etoposide treatment. Etoposide 127-136 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 30716336-8 2019 Furthermore, IL-8 inhibition by its antibody increased the sensitivity of AML cells to cell death triggered via etoposide. Etoposide 112-121 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 30871567-12 2019 The levels of TNF-a, IL-6, and IL-8 were positively correlated with increases in BMI, serum glucose and cholesterol levels. Glucose 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 30871567-12 2019 The levels of TNF-a, IL-6, and IL-8 were positively correlated with increases in BMI, serum glucose and cholesterol levels. Cholesterol 104-115 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 30867499-0 2019 The BRAF-inhibitor PLX4720 inhibits CXCL8 secretion in BRAFV600E mutated and normal thyroid cells: a further anti-cancer effect of BRAF-inhibitors. PLX 4720 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 30767051-8 2019 In contrast, while the silica response was not augmented in the A549 cells by the addition of iron oxide, iron oxide particles alone were sufficient to induce IL-8 production in these cells. ferric oxide 106-116 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 30797069-0 2019 Sinomenine inhibits osteolysis in breast cancer by reducing IL-8/CXCR1 and c-Fos/NFATc1 signaling. sinomenine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 30984167-15 2019 Peficitinib decreased also the MMP-3, CXCL8, and CXCL1 release at 5 muM. peficitinib 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 31061956-6 2019 Spearman correlations of change of an immune marker from baseline to day 90 with change in serum bilirubin revealed that an increase in total bilirubin correlated with 1) increased percentage of HLA-DR+CD38+ NK cells and expression of NK cell activation markers CD69 and HLA-DR, 2) decreased percentage of regulatory T cells, and 3) increased interleukin (IL)-8 and associated neutrophil products (elastase and neutrophil extracellular traps). Bilirubin 142-151 C-X-C motif chemokine ligand 8 Homo sapiens 343-361 30936860-9 2019 Treatment of differentiated Caco-2 cells monolayer with BGZLS10-17 supernatant containing GABA alleviated inflammation (production of IL-8) caused by IL-1beta and significantly stimulated the expression of tight junction proteins (zonulin, occludin, and claudin 4), as well as the expression of TGF-beta cytokine leading to the conclusion that immunosuppression and strengthening the tight junctions can have significant role in the maintenance of intestinal epithelial barrier integrity. gamma-Aminobutyric Acid 90-94 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 30972180-6 2019 PA significantly increased several markers of the inflammatory and profibrotic process including gene expression of collagens, alpha-sma, tissue inhibitor of matrix metalloprotease 1 (timp1) and the stellate cell activation marker pdgfrbeta as well as secreted CXCL8 (IL8) levels. Palmitic Acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 261-266 30972180-6 2019 PA significantly increased several markers of the inflammatory and profibrotic process including gene expression of collagens, alpha-sma, tissue inhibitor of matrix metalloprotease 1 (timp1) and the stellate cell activation marker pdgfrbeta as well as secreted CXCL8 (IL8) levels. Palmitic Acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 268-271 31057757-4 2019 Here we present an extremely simple approach to introduce a compact NaF-rich interphase on a Na surface via chemical reactions between fluoroethylene carbonate-Na+ and Na metal, resulting in a compatible Na anode/SN-based electrolyte interface. 4-fluoro-1,3-dioxolan-2-one 135-159 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 30726064-7 2019 The CXCL8-Glu4AlaLeu5AlaArg6His analogue was inactive in cells expressing CXCR1 and CXCR2. glu4alaleu5alaarg6his 10-31 C-X-C motif chemokine ligand 8 Homo sapiens 4-9 31057757-4 2019 Here we present an extremely simple approach to introduce a compact NaF-rich interphase on a Na surface via chemical reactions between fluoroethylene carbonate-Na+ and Na metal, resulting in a compatible Na anode/SN-based electrolyte interface. na metal 168-176 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 30726064-8 2019 These findings suggest that the Glu4Leu5 motif in CXCL8 is essential for activation of CXCR1 and CXCR2. glu4leu5 32-40 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 31057757-4 2019 Here we present an extremely simple approach to introduce a compact NaF-rich interphase on a Na surface via chemical reactions between fluoroethylene carbonate-Na+ and Na metal, resulting in a compatible Na anode/SN-based electrolyte interface. succinonitrile 213-215 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 31057757-5 2019 The in situ formed NaF-rich interphase can not only prevent side reactions between the SN-based electrolyte and Na anode but also regulate the uniform deposition of dendrite-free Na. sn-based electrolyte 87-107 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 30726064-9 2019 Importantly, CXCL8-Glu4AlaLeu5AlaArg6His blocked specifically the calcium release and chemotaxis of cells expressing CXCR1 but not of cells expressing CXCR2. Calcium 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 13-18 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Zinc 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Zinc 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Zinc 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 119-126 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 119-126 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 119-126 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. zinc chloride 139-144 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. zinc chloride 139-144 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. zinc chloride 139-144 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 188-195 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 188-195 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 188-195 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 188-195 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 188-195 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30726064-11 2019 The binding of CXCL8-ELR6H to CXCR1 created a Zn2+ coordination site at the receptor activation domain responsible for calcium release, as ZnCl2 specifically blocked CXCL8-Arg6His-induced calcium release without affecting CXCL8-induced calcium release. Calcium 188-195 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 30857165-1 2019 18F-Sodium Fluoride (NaF) accumulates in areas of active hydroxyapatite deposition and potentially unstable atherosclerotic plaques. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 30832675-11 2019 This change in GSK-3 activity decreased the C/EBPss phosphorylation levels of the threonine 235, a residue whose phosphorylation is known to increase C/EBPss transactivation potential, and consequently modified IL-8 expression. Threonine 82-91 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 30915077-5 2019 PMA-induced NETs were decorated with annexins, azurocidin and histone H3, whereas A23187-induced NETs were decorated with granule proteins including CAMP/LL37, CRISP3, lipocalin and MMP8, histones H1.0, H1.4, and H1.5, interleukin-8, protein-arginine deiminase-4 (PADI4), and alpha-enolase. Calcimycin 82-88 C-X-C motif chemokine ligand 8 Homo sapiens 219-232 30866458-9 2019 In particular, menadione inhibited nuclear factor kappa-light-chain-enhancer of activated B cell (NF-kappaB) activation and thereby reduced expression of the proinflammatory cytokines such as IL-1beta, IL-6, IL-8, and TNF-alpha in AGS as well as in THP-1 (monocytic leukemia cell) cell lines. Vitamin K 3 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 30866565-5 2019 Several fatty acids were associated with interferon-gamma (IFNgamma) and interleukins (ILs) IL-6, IL-8, and IL-10 at baseline and additionally also with IL-1b at 1 year. Fatty Acids 8-19 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 30866565-6 2019 Omega-6 fatty acids were consistently positively associated with pro-inflammatory IL-6 and IL-8 at baseline. Fatty Acids, Omega-6 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 30341773-10 2019 CONCLUSION: Resting salivary flow rate was significantly reduced in head-and-neck cancer patients following radiotherapy and use of CPP-ACP with SnF2 /NaF significantly lowered caries progression compared with SnF2 /NaF alone. cpp-acp 132-139 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 30553868-6 2019 IL-8 secretion was inhibited by intracellular TLR4-domain antagonist TAK-242 with an IC50-value of 259.6 nM, by ecto-domain TLR4 antagonistic mianserin with 10-51 muM and by anti-CD14-IgA. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30659323-3 2019 Here in human neuroblastoma SH-SY5Y cells treated with sodium fluoride (NaF, 20, 40 and 60 mg/L), mitochondrial fission suppression exerted a central role in NaF-induced mitochondrial abnormalities and the resulting autophagy deficiency, apoptosis augmentation, and compromised neuronal survival. Sodium Fluoride 55-70 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 30659323-3 2019 Here in human neuroblastoma SH-SY5Y cells treated with sodium fluoride (NaF, 20, 40 and 60 mg/L), mitochondrial fission suppression exerted a central role in NaF-induced mitochondrial abnormalities and the resulting autophagy deficiency, apoptosis augmentation, and compromised neuronal survival. Sodium Fluoride 55-70 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 30659323-7 2019 Consistently, using Sprague-Dawley rats developmentally exposed to NaF (10, 50, and 100 mg/L) from pre-pregnancy until 2 months of delivery to mimic human exposure, we showed that perinatal exposure to environmentally relevant levels of fluoride caused learning and memory impairments, accompanied by hippocampal mitochondrial morphological alterations manifested as fission suppression and fusion acceleration, along with defective autophagy, excessive apoptosis and neuronal loss. Fluorides 237-245 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 30626802-5 2019 Consistent with decreased expression of TLR2, PGN-dependent interleukin-8 (IL-8) gene up-regulation was markedly reduced by 40 microM of curcumin treatment. Curcumin 137-145 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 30594784-6 2019 The addition of zafirlukast to culture media suppressed TNF-alpha-induced expression of endothelial vascular adhesion molecules, such as ICAM-1, VCAM-1, and induction of cytokines, including IL-1beta, IL-6, and IL-8. zafirlukast 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 30626802-5 2019 Consistent with decreased expression of TLR2, PGN-dependent interleukin-8 (IL-8) gene up-regulation was markedly reduced by 40 microM of curcumin treatment. Curcumin 137-145 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 30265130-11 2019 A statistically significant decrease in IL-8 was noted for all TiO2NP at the highest concentrations due to the adsorption of IL-8 by TiO2. tio2np 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 30944833-7 2019 Furthermore, OCT reduced both pro- and anti-inflammatory mediators (IL-8, IL-33, and IL-10), while angiogenesis and growth factor mediators (VEGF and TGF-beta1) remained unchanged in skin explant cultures. octenidine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 30148447-2 2019 This study determined monosodium urate crystal-induced MIF production and its interaction with interleukin (IL)-8 in gout. Uric Acid 22-38 C-X-C motif chemokine ligand 8 Homo sapiens 95-113 30265130-11 2019 A statistically significant decrease in IL-8 was noted for all TiO2NP at the highest concentrations due to the adsorption of IL-8 by TiO2. tio2np 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 30478770-7 2019 Multiple linear regression models predicted significant association between transcript levels of Ki-67, NF-kB (p65), PPARgamma, COX-2 and IL-8, CDC25A, and CXCL10 with duration of drug (5-ASA) exposure (P <= 0.05). Mesalamine 186-191 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 30265130-11 2019 A statistically significant decrease in IL-8 was noted for all TiO2NP at the highest concentrations due to the adsorption of IL-8 by TiO2. titanium dioxide 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 30265130-11 2019 A statistically significant decrease in IL-8 was noted for all TiO2NP at the highest concentrations due to the adsorption of IL-8 by TiO2. titanium dioxide 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 30354488-4 2019 The p65 subunit of NF-kappaB was translocated into the nucleus of the cells treated with 100 microg mL-1 PM2.5 at 6 and 24 h. Bay11-7082 partly inhibited PM2.5-induced increases of IL-6 and IL-8 secretion. 3-(4-methylphenylsulfonyl)-2-propenenitrile 126-136 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 30964194-10 2019 The cytoprotective effects of SDX resulted from a reduction in a) ROS production, b) neo-synthesis and release of pro-inflammatory cytokines (TNFalpha, IL1, IL6, IL8), c) DNA damage induced by MGO or IR. glucuronyl glucosamine glycan sulfate 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 30783447-8 2019 Notably, IL-8 was positively correlated with AHI, morning systolic and diastolic pressure (r=0.337, 0.413 and 0.629; P<0.05), and negatively correlated with MSaO2 and LSaO2 (r=-0.329 and -0.417; P<0.05). msao2 160-165 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 30783447-8 2019 Notably, IL-8 was positively correlated with AHI, morning systolic and diastolic pressure (r=0.337, 0.413 and 0.629; P<0.05), and negatively correlated with MSaO2 and LSaO2 (r=-0.329 and -0.417; P<0.05). lsao2 170-175 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 31777853-1 2019 Objectives: This study aimed to assess the effect of 0.05% sodium fluoride (NaF) mouthwash on the surface roughness and friction between ceramic brackets and rhodium-coated (RC) and uncoated stainless steel (SS) wires. Sodium Fluoride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 31777853-1 2019 Objectives: This study aimed to assess the effect of 0.05% sodium fluoride (NaF) mouthwash on the surface roughness and friction between ceramic brackets and rhodium-coated (RC) and uncoated stainless steel (SS) wires. Rhodium 158-165 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 30443903-0 2019 L-selectin expression is regulated by CXCL8-induced reactive oxygen species produced during human neutrophil rolling. Reactive Oxygen Species 52-75 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 30443903-4 2019 Flow experiments using dihydroethidium-preloaded human neutrophils showed that these cells initiate an early production of intracellular ROS during the rolling phase of the adhesion cascade, a phenomenon that required cell rolling, and the interaction of the chemokine receptor CXCR2 with their ligand CXCL8. dihydroethidium 23-38 C-X-C motif chemokine ligand 8 Homo sapiens 302-307 30443903-4 2019 Flow experiments using dihydroethidium-preloaded human neutrophils showed that these cells initiate an early production of intracellular ROS during the rolling phase of the adhesion cascade, a phenomenon that required cell rolling, and the interaction of the chemokine receptor CXCR2 with their ligand CXCL8. Reactive Oxygen Species 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 302-307 30443903-8 2019 These findings indicate that, in response to CXCL8, neutrophils initiate ROS production during the rolling phase of the inflammatory response. Reactive Oxygen Species 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 45-50 30059697-8 2019 A 30% increase in IL-8 suppression by FLU (P = .04) and a trend for increased TNF-alpha suppression by FLU between V0 and V6 (P = .07) were observed in patients with easy-to-control asthma. Fluticasone 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 30686699-9 2019 Patients treated with azithromycin demonstrated less airway inflammation, with lower bronchoalveolar lavage (BAL) neutrophilia and BAL interleukin-8 protein levels at Day 30 (p = 0.09 and p = 0.04, respectively) and Day 90 (p = 0.002 and p = 0.08, respectively) after LTx. Azithromycin 22-34 C-X-C motif chemokine ligand 8 Homo sapiens 135-148 30378164-12 2019 In HCT 116 cells stimulated with TNF-alpha, TUDCA significantly inhibited IL-8 and IL-1alpha expression and suppressed TNF-alpha-induced IkappaBalpha phosphorylation/degradation and DNA-binding activity of NF-kappaB. ursodoxicoltaurine 44-49 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 30761568-9 2019 Levels of IL-6 and IL-8 were significantly lower in TG than CG at 3 months. Thioguanine 52-54 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 30569138-7 2019 Treatment of HepG2 cells for 5 h with the BA-loaded liposomes coated with chitosan at 5 mM lowered the extent of the increase in IL-8, IL-6, TNF-alpha and TGF-beta expression of approximately 64, 58, 85 and 73.8%, respectively, when compared to the untreated cells. Butyric Acid 42-44 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 30139886-1 2019 Our objective was to test the hypothesis that variability in SUV normalized by skeletal volume (SV) in 18F-fluoride (18F-NaF) PET/CT studies is lower than variability in SUV normalized by body weight (BW). Fluoride ion f-18 103-115 C-X-C motif chemokine ligand 8 Homo sapiens 121-124 30882648-1 2019 F-18 sodium-fluoride (NaF) bone positron emission tomography (PET/CT) has been used for diagnosing various bone and joint diseases, and, with using dual-phase scan protocol, it could give the same information obtained by the 3-phase bone scintigraphy. Sodium Fluoride 5-20 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 30519866-7 2019 Our data show that dopamine treatment of human macrophages isolated from healthy and cART-treated donors promotes production of inflammatory mediators including IL-1beta, IL-6, IL-18, CCL2, CXCL8, CXCL9, and CXCL10. Dopamine 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 190-195 30269694-6 2019 The rapid release of CXCL-8, a preformed chemokine contained in Weibel-Palade bodies, confirmed that haemozoin induces a perturbation of the intracellular endothelial trafficking, including the exocytosis of MTT-formazan containing vesicles. MTT formazan 208-220 C-X-C motif chemokine ligand 8 Homo sapiens 21-27 30629076-0 2019 Glycosylated naphthalimides and naphthalimide Troger"s bases as fluorescent aggregation probes for Con A. Herein we report the synthesis of fluorescent, glycosylated 4-amino-1,8-naphthalimide (Nap) 1, and the related 1,8-naphthalimides Troger"s bases (TBNap) 2 and 3, from 1,8-naphthalic anhydride precursors, the alpha-mannosides being introduced through the use of CuAAC mediated "click" chemistry. Naphthalimides 13-27 C-X-C motif chemokine ligand 8 Homo sapiens 166-199 30547277-10 2019 Using an ATP model of stimulation, we further demonstrated that extracellular ATP stimulation to IL-1beta containing LPS microparticles induces release of its content, which when subjected to epithelial cells induced IL-8. Adenosine Triphosphate 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 30547277-10 2019 Using an ATP model of stimulation, we further demonstrated that extracellular ATP stimulation to IL-1beta containing LPS microparticles induces release of its content, which when subjected to epithelial cells induced IL-8. Adenosine Triphosphate 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 30653318-0 2019 Eupatoriopicrin Inhibits Pro-inflammatory Functions of Neutrophils via Suppression of IL-8 and TNF-alpha Production and p38 and ERK 1/2 MAP Kinases. eupatoriopicrine 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 30629076-0 2019 Glycosylated naphthalimides and naphthalimide Troger"s bases as fluorescent aggregation probes for Con A. Herein we report the synthesis of fluorescent, glycosylated 4-amino-1,8-naphthalimide (Nap) 1, and the related 1,8-naphthalimides Troger"s bases (TBNap) 2 and 3, from 1,8-naphthalic anhydride precursors, the alpha-mannosides being introduced through the use of CuAAC mediated "click" chemistry. alpha-mannosides 314-330 C-X-C motif chemokine ligand 8 Homo sapiens 166-199 30629076-0 2019 Glycosylated naphthalimides and naphthalimide Troger"s bases as fluorescent aggregation probes for Con A. Herein we report the synthesis of fluorescent, glycosylated 4-amino-1,8-naphthalimide (Nap) 1, and the related 1,8-naphthalimides Troger"s bases (TBNap) 2 and 3, from 1,8-naphthalic anhydride precursors, the alpha-mannosides being introduced through the use of CuAAC mediated "click" chemistry. tbnap 252-257 C-X-C motif chemokine ligand 8 Homo sapiens 166-199 30629076-0 2019 Glycosylated naphthalimides and naphthalimide Troger"s bases as fluorescent aggregation probes for Con A. Herein we report the synthesis of fluorescent, glycosylated 4-amino-1,8-naphthalimide (Nap) 1, and the related 1,8-naphthalimides Troger"s bases (TBNap) 2 and 3, from 1,8-naphthalic anhydride precursors, the alpha-mannosides being introduced through the use of CuAAC mediated "click" chemistry. 8-naphthalic anhydride 275-297 C-X-C motif chemokine ligand 8 Homo sapiens 166-199 30765785-2 2019 This study systematically reviewed the dentine caries arrest capabilities of silver diamine fluoride (SDF) and sodium fluoride (NaF). Sodium Fluoride 111-126 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 30778158-9 2019 In addition, our results indicated that iron overload enhanced the release of interleukin-8 (IL-8), a chemokine that activates neutrophils, and subsequently elevated intracellular calcium concentration ([Ca2+]i). Iron 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 30778158-9 2019 In addition, our results indicated that iron overload enhanced the release of interleukin-8 (IL-8), a chemokine that activates neutrophils, and subsequently elevated intracellular calcium concentration ([Ca2+]i). Iron 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 30778158-11 2019 These findings suggest that the iron overload caused by engulfed MWCNTs results in the increase of IL-8 production and the elevation of [Ca2+]i, thereby activating the mitochondria-mediated apoptotic pathway. Iron 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 30828266-0 2019 Extracellular acidification-induced CXCL8 production through a proton-sensing receptor OGR1 in human airway smooth muscle cells: a response inhibited by dexamethasone. Dexamethasone 153-166 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 30828266-7 2019 CXCL8 secreted from ASMCs was measured by enzyme-linked immunosorbent assay (ELISA). asmcs 20-25 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 30828266-10 2019 ASMCs transfected with small interfering RNA (siRNA) targeted for OGR1 produced less CXCL8 compared with those transfected with non-targeting siRNA. asmcs 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 85-90 30828266-11 2019 Protein kinase C (PKC) inhibitor, MEK1/2 inhibitor, and the inhibitor of IkappaB phosphorylation reduced acidic pH-stimulated CXCL8 production in ASMCs. asmcs 146-151 C-X-C motif chemokine ligand 8 Homo sapiens 126-131 30828266-12 2019 Dexamethasone also inhibited acidic pH-stimulated CXCL8 production of ASMCs in a dose-dependent manner. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 30828266-12 2019 Dexamethasone also inhibited acidic pH-stimulated CXCL8 production of ASMCs in a dose-dependent manner. asmcs 70-75 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 30828266-14 2019 Conclusions: CXCL8 released from ASMCs by extracellular acidification may play a pivotal role in airway accumulation of neutrophils. asmcs 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 13-18 30767218-7 2019 ALP activity, ALP protein, and messenger RNA (mRNA) expression showed that 0.5 mM was the optimal concentration for the induction of SCAPs by NaF. scaps 133-138 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 30767218-8 2019 0.5 mM NaF-treated SCAPs induced more mineralized nodules as compared with untreated cells. scaps 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 7-10 30765814-0 2019 Metformin inhibits lithocholic acid-induced interleukin 8 upregulation in colorectal cancer cells by suppressing ROS production and NF-kB activity. Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 30765814-0 2019 Metformin inhibits lithocholic acid-induced interleukin 8 upregulation in colorectal cancer cells by suppressing ROS production and NF-kB activity. Lithocholic Acid 19-35 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 30765814-0 2019 Metformin inhibits lithocholic acid-induced interleukin 8 upregulation in colorectal cancer cells by suppressing ROS production and NF-kB activity. Reactive Oxygen Species 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 30765814-2 2019 In this study, we describe the inhibitory effect of metformin in interleukin 8 (IL-8) upregulation by lithocholic acid (LCA) in HCT116 colorectal cancer (CRC) cells. Metformin 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 30765814-2 2019 In this study, we describe the inhibitory effect of metformin in interleukin 8 (IL-8) upregulation by lithocholic acid (LCA) in HCT116 colorectal cancer (CRC) cells. Metformin 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30765814-2 2019 In this study, we describe the inhibitory effect of metformin in interleukin 8 (IL-8) upregulation by lithocholic acid (LCA) in HCT116 colorectal cancer (CRC) cells. Lithocholic Acid 102-118 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 30765814-2 2019 In this study, we describe the inhibitory effect of metformin in interleukin 8 (IL-8) upregulation by lithocholic acid (LCA) in HCT116 colorectal cancer (CRC) cells. Lithocholic Acid 102-118 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30765814-2 2019 In this study, we describe the inhibitory effect of metformin in interleukin 8 (IL-8) upregulation by lithocholic acid (LCA) in HCT116 colorectal cancer (CRC) cells. Lithocholic Acid 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 30765814-2 2019 In this study, we describe the inhibitory effect of metformin in interleukin 8 (IL-8) upregulation by lithocholic acid (LCA) in HCT116 colorectal cancer (CRC) cells. Lithocholic Acid 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30765814-3 2019 Pharmacological inhibition studies indicated that reactive oxygen species (ROS) were involved in LCA-induced IL-8 upregulation through activation of the transcription factor NF-kappaB. Reactive Oxygen Species 50-73 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 30765814-3 2019 Pharmacological inhibition studies indicated that reactive oxygen species (ROS) were involved in LCA-induced IL-8 upregulation through activation of the transcription factor NF-kappaB. Reactive Oxygen Species 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 30702103-6 2019 And in medium-polarity solvents, because of the relatively weaker solvation-induced stabilization of the CT state, its energy could be equal to or slightly lower than that of the LE state, leading to a smaller driving force for LE CT interconversion; therefore complete LE CT interconversion cannot take place. Carbon Tetrachloride 105-107 C-X-C motif chemokine ligand 8 Homo sapiens 228-235 30765814-3 2019 Pharmacological inhibition studies indicated that reactive oxygen species (ROS) were involved in LCA-induced IL-8 upregulation through activation of the transcription factor NF-kappaB. Lithocholic Acid 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 30765814-4 2019 Metformin was demonstrated to block LCA-stimulated ROS production, in turn suppressing NF-kappaB signaling that was critical for IL-8 upregulation. Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 30765814-4 2019 Metformin was demonstrated to block LCA-stimulated ROS production, in turn suppressing NF-kappaB signaling that was critical for IL-8 upregulation. Lithocholic Acid 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 30765814-7 2019 In conclusion, metformin inhibited NADPH oxidase, which in turn suppressed ROS production and NF-kappaB activation to prevent IL-8 upregulation stimulated by LCA; this prevention thus obstructed endothelial cell proliferation and tubelike formation. Metformin 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 30765814-7 2019 In conclusion, metformin inhibited NADPH oxidase, which in turn suppressed ROS production and NF-kappaB activation to prevent IL-8 upregulation stimulated by LCA; this prevention thus obstructed endothelial cell proliferation and tubelike formation. Lithocholic Acid 158-161 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 30702103-6 2019 And in medium-polarity solvents, because of the relatively weaker solvation-induced stabilization of the CT state, its energy could be equal to or slightly lower than that of the LE state, leading to a smaller driving force for LE CT interconversion; therefore complete LE CT interconversion cannot take place. Carbon Tetrachloride 105-107 C-X-C motif chemokine ligand 8 Homo sapiens 272-279 30761406-5 2019 RESULTS: SLNs provided significant encapsulation of atRA and also sustained its release over 72 h. A549 cells were viable following the addition of atRA SLNs and showed a reduction in IL-6 and IL-8 levels. Tretinoin 148-152 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 30624061-7 2019 By using this ultrasensitive SERS-microdroplet method, the VEGF and IL-8 secretions from several cells in one droplet were explored and the data show that the cell-cell interaction may promote angiogenesis of cancer cells through the up-regulation of VEGF and IL-8. sers 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 30809216-13 2019 Finally, PGE2 treatment in THP-1 cells triggered downmodulation of pro-inflammatory mediators and upregulation of IL-8 and IL-10. Dinoprostone 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 30733507-4 2019 Long-term treatment of olanzapine caused metabolic symptoms, including IR, by markedly elevating the plasma levels of pro-inflammatory cytokines, including IL-1ss, IL-6, IL-8 and TNFalpha; these findings are consistent with observations from schizophrenia patients chronically treated with olanzapine. Olanzapine 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 30719765-6 2019 The results showed that erlotinib alleviated CXCL8-induced metastasis of the colon cancer cells. Erlotinib Hydrochloride 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 45-50 30624061-7 2019 By using this ultrasensitive SERS-microdroplet method, the VEGF and IL-8 secretions from several cells in one droplet were explored and the data show that the cell-cell interaction may promote angiogenesis of cancer cells through the up-regulation of VEGF and IL-8. sers 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 260-264 30580559-3 2019 Approach and Results- We performed coronary atherosclerosis with 18F-sodium fluoride (NaF) positron emission tomography/computed tomography and gated chest computed tomography for coronary artery calcium in 88 consecutive ambulatory patients with DM on a stable medical regimen. 18f-sodium fluoride 65-84 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 30549424-7 2019 By maintaining the same topology as the parental cells, these dexamethasone-loaded ghost nanovesicles derived from human U937 monocytes reduce the release of interleukin-8 from OMV-treated endothelial cells in vitro, and mitigate the symptoms of OMV-induced SIRS in vivo. Dexamethasone 62-75 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 30549424-7 2019 By maintaining the same topology as the parental cells, these dexamethasone-loaded ghost nanovesicles derived from human U937 monocytes reduce the release of interleukin-8 from OMV-treated endothelial cells in vitro, and mitigate the symptoms of OMV-induced SIRS in vivo. 1-ethylcyclopentyl [(2R,6S,12Z,13aS,14aR,16aS)-2-[(7-methoxy-3-methylquinoxalin-2-yl)oxy]-14a-{[(1-methylcyclopropyl)sulfonyl]carbamoyl}-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-6-yl]carbamate 177-180 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 30580559-5 2019 NaF activity was measured as target (coronary arteries)-to-background (left ventricular pool) ratio (TBR). tbr 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 30340750-0 2019 The clinical significance of incidental soft tissue uptake on whole body 18F-sodium fluoride bone PET-CT. 18F-sodium fluoride (NaF) is a PET bone imaging agent and is commonly used in imaging patients with cancer; however, similar to technetium-99m medronic acid (99mTc-MDP), it can be useful in the evaluation of benign bone and joint conditions. Sodium Fluoride 77-92 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 30312114-5 2019 In human myometrial cells, simvastatin reduced proinflammatory mediator mRNA and protein expression (IL-6 and IL-8) and increased anti-inflammatory cytokine mRNA expression (IL-10 and IL-13). Simvastatin 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 30622078-9 2019 Additionally, peripheral counts of white blood cells, and the concentrations of interleukin-8 and tumor necrosis factor-alpha, in Guiyu children were greater than in Haojiang children, and were positively associated with CDI. 1,1'-Carbonyldiimidazole 221-224 C-X-C motif chemokine ligand 8 Homo sapiens 80-125 30585659-6 2019 We demonstrate that dapsone suppresses production of specific cytokine signatures interleukin (IL)1alpha and IL8 in human epidermal keratinocytes and IL1beta, IL6, IL8 and tumor necrosis factor-alpha in THP-1 cells in response to P. acnes. Dapsone 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 29512317-1 2019 FOCUS QUESTION: What is the efficacy of a chlorhexidine (CHX) mouthwash (MW) containing sodium fluoride (NaF) compared to a CHX - MW alone on the parameters of plaque, gingivitis and discoloration? Chlorhexidine 42-55 C-X-C motif chemokine ligand 8 Homo sapiens 105-108 30698875-8 2019 Furthermore, CPs caused alterations of mRNA expression levels of dermal matrix-related proteins, such as upregulating MMP-1 and IL-8. cps 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 29512317-1 2019 FOCUS QUESTION: What is the efficacy of a chlorhexidine (CHX) mouthwash (MW) containing sodium fluoride (NaF) compared to a CHX - MW alone on the parameters of plaque, gingivitis and discoloration? Sodium Fluoride 88-103 C-X-C motif chemokine ligand 8 Homo sapiens 105-108 29512317-1 2019 FOCUS QUESTION: What is the efficacy of a chlorhexidine (CHX) mouthwash (MW) containing sodium fluoride (NaF) compared to a CHX - MW alone on the parameters of plaque, gingivitis and discoloration? Chlorhexidine 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 105-108 30378182-10 2019 Following inflammatory stimulation and treatment with ASA CM, tenocytes downregulated IL-8 gene expression, a pro-inflammatory cytokine normally elevated during the inflammatory phase of tendon healing. Aspirin 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 30078219-5 2019 Further, significant increase in phosphorylation of signal transducer and activator of transcription 1 (STAT-1) and STAT-3 (both at ser727 residue) is observed on treating HTR-8/SVneo cells with 25 microM of H2 O2 accompanied by an increase in the secretion of interleukin-8 (IL-8) and macrophage inflammatory protein-1beta (MIP-1beta). Hydrogen Peroxide 208-213 C-X-C motif chemokine ligand 8 Homo sapiens 261-274 30078219-5 2019 Further, significant increase in phosphorylation of signal transducer and activator of transcription 1 (STAT-1) and STAT-3 (both at ser727 residue) is observed on treating HTR-8/SVneo cells with 25 microM of H2 O2 accompanied by an increase in the secretion of interleukin-8 (IL-8) and macrophage inflammatory protein-1beta (MIP-1beta). Hydrogen Peroxide 208-213 C-X-C motif chemokine ligand 8 Homo sapiens 276-280 30078219-6 2019 A significant decrease in H2 O2 -mediated invasion of HTR-8/SVneo cells and reduced expression of IL-8 and MIP-1beta accompanied by decrease in MMP-9/TIMP-1 ratio are observed on inhibiting STAT-1 and STAT-3 by small interfering RNA (siRNA). Hydrogen Peroxide 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 30078219-8 2019 Inhibition of IL-8 and MIP-1beta by siRNA also leads to a significant decrease in both basal and H2 O2 -mediated invasion. Hydrogen Peroxide 97-102 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 30078219-9 2019 Interestingly, inhibition of MIP-1beta by siRNA leads to a significant reduction in H2 O2 -mediated increase in IL-8. Hydrogen Peroxide 84-89 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 30078219-11 2019 From the above results, it can be concluded that H2 O2 activates STAT signaling, MIP-1beta & IL-8 secretion and increases MMP-9/TIMP-1 ratio leading to an increased invasion of HTR-8/SVneo cells without affecting their viability. Hydrogen Peroxide 49-54 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 30553912-5 2019 In addition, we found that the mRNA expression of IL-1beta, IL-6, IL-8 and IL-17A were markedly down-regulated by treatment with betulinic acid in TNF-alpha-induced RA FLSs. betulinic acid 129-143 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 30305725-0 2019 IL-8-induced O-GlcNAc modification via GLUT3 and GFAT regulates cancer stem cell-like properties in colon and lung cancer cells. o-glcnac 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30476578-5 2019 The results demonstrated that plantamajoside decreased the production of PGE2, NO, IL-6, and IL-8 in LPS-stimulated HGFs. plantamajoside 30-44 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 30030777-6 2019 Nicotine, 4-NQO, and their combinational applications with Pg LPS induced the secretions of IL-1beta and IL-1Ra, while that of IL-8 was inhibited by the presence of Pg LPS. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 30030777-6 2019 Nicotine, 4-NQO, and their combinational applications with Pg LPS induced the secretions of IL-1beta and IL-1Ra, while that of IL-8 was inhibited by the presence of Pg LPS. 4-Nitroquinoline-1-oxide 10-15 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 30305725-6 2019 We also showed that IL-8 stimulation of colon and lung cancer cells-induced glucose uptake and expressions of glucose transporter 3 (GLUT3) and glucosamine fructose-6-phosphate aminotransferase (GFAT), a regulator of glucose flux to the hexosamine biosynthetic pathway, resulting in enhancement of protein O-GlcNAcylation. Glucose 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 30305725-6 2019 We also showed that IL-8 stimulation of colon and lung cancer cells-induced glucose uptake and expressions of glucose transporter 3 (GLUT3) and glucosamine fructose-6-phosphate aminotransferase (GFAT), a regulator of glucose flux to the hexosamine biosynthetic pathway, resulting in enhancement of protein O-GlcNAcylation. Glucose 110-117 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 30305725-6 2019 We also showed that IL-8 stimulation of colon and lung cancer cells-induced glucose uptake and expressions of glucose transporter 3 (GLUT3) and glucosamine fructose-6-phosphate aminotransferase (GFAT), a regulator of glucose flux to the hexosamine biosynthetic pathway, resulting in enhancement of protein O-GlcNAcylation. Hexosamines 237-247 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 30719005-5 2018 Oleic acid alone had opposite effects due to its different capacity of controlling these metabolic pathways, in particular by reduction of the ROS levels and MMP-2 activity, down-regulation of BiP, eIF2alpha, ATF6, XBP1u, CHOP, IL6, IL8 and by SOD2 and PTP-1B overexpression. Oleic Acid 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 233-236 30674715-7 2019 Furthermore, GL-2045 administration to nonhuman primates (NHPs) transiently increased systemic levels of the antiinflammatory cytokines IL-10 and IL-1RA, reduced the proinflammatory cytokine IL-8, and decreased surface expression of CD14 and HLA-DR on monocytes. glycylleucine 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 30592197-8 2019 The NaF/KF-PDT-induced changes in the HAXPES spectra for different alkali exposures are best reproduced by additional contributions from KInSe2, with some indications that the formation of a pronounced K-In-Se-type surface species might crucially depend on the amount of K available during PDT. Selenium 140-142 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 30247740-4 2019 TVX inhibited find-me signal release in apoptotic HepG2 hepatocytes, decelerated freshly isolated human neutrophils toward IL-8 and f-MLF, and decreased the liver expression of ICAM-1. trovafloxacin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 30782274-9 2019 TAK-242 inhibited the mRNA and protein expression of TLR4 and NF-kappaB and mRNA expression of IL-8 (P<0.05). ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 30782274-12 2019 Glycyrrhizin inhibited the mRNA expression of HMGB1 and the mRNA and protein expression of TLR4 and NF-kappaB and then reduced the mRNA expression of IL-8 (P<0.05). Glycyrrhizic Acid 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 30670536-6 2019 Platelets treated with aspirin did not activate the Akt pathway, resulting in reduced IL-8 secretion and impaired tumor cell invasion. Aspirin 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 30670536-7 2019 Of note, patients with breast cancer receiving aspirin had lower circulating IL-8, and their platelets did not increase tumor cell invasion compared with patients not receiving aspirin. Aspirin 47-54 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 30719005-6 2018 The supplementation of saturated palmitic acid with the monounsaturated oleic acid reversed the negative effects of palmitic acid alone regulating insulin secretion from pancreatic beta cells through ROS, MMP-2, ATF6, XBP1u, IL8 reduction and SOD2, PTP-1B activation. saturated palmitic acid 23-46 C-X-C motif chemokine ligand 8 Homo sapiens 225-228 30719005-6 2018 The supplementation of saturated palmitic acid with the monounsaturated oleic acid reversed the negative effects of palmitic acid alone regulating insulin secretion from pancreatic beta cells through ROS, MMP-2, ATF6, XBP1u, IL8 reduction and SOD2, PTP-1B activation. monounsaturated oleic acid 56-82 C-X-C motif chemokine ligand 8 Homo sapiens 225-228 30719005-6 2018 The supplementation of saturated palmitic acid with the monounsaturated oleic acid reversed the negative effects of palmitic acid alone regulating insulin secretion from pancreatic beta cells through ROS, MMP-2, ATF6, XBP1u, IL8 reduction and SOD2, PTP-1B activation. Palmitic Acid 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 225-228 30687301-8 2018 Levels of pro-inflammatory cytokines IL-8 and TNFalpha were also increased in DHF patients as compared with those in healthy and DF subjects. dhf 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 30646963-0 2019 Genistein inhibits stemness of SKOV3 cells induced by macrophages co-cultured with ovarian cancer stem-like cells through IL-8/STAT3 axis. Genistein 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 30646963-7 2019 Moreover, depletion or addition of IL-8 enhanced or attenuated the effect of GEN. Additionally, knockdown or overepression of STAT3 in THP-1 macrophages potentiated or attenuated the inhibitory effects of GEN. Genistein 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 30622698-6 2019 In vitro experiments demonstrated that PLAG inhibited NADPH oxidase 2 (NOX2)-mediated reactive oxygen species production induced by gemcitabine, which is the upstream of MIP-2 and/or CXCL8. gemcitabine 132-143 C-X-C motif chemokine ligand 8 Homo sapiens 183-188 30397077-5 2019 When senescent, luminal cells activated stromal fibroblasts in an IL-8-dependent manner, through the activation of the STAT3 pathway. Phenobarbital 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 30397077-7 2019 These results show the role of senescent breast luminal cells in promoting the inflammatory/carcinogenic microenvironment through the activation of fibroblasts in an IL-8-dependent manner. Phenobarbital 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 29929938-0 2019 PGE2 enhanced TNFalpha-mediated IL-8 induction in monocytic cell lines and PBMC. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 30407866-6 2019 On the contrary, challenge with supraphysiological concentrations (10-25 mM), as might be used therapeutically, of propionate or butyrate in combination with TNFalpha resulted in substantially greater IL-6 and CXCL8 release from HLFs and ASM cells than challenge with TNFalpha alone, demonstrating synergistic effects. Propionates 115-125 C-X-C motif chemokine ligand 8 Homo sapiens 210-215 30384152-10 2019 Intriguingly, both resveratrol and JNK inhibitor SP600125 suppressed TNFalpha-induced IL6 and IL8 mRNA expression (P < 0.05). Resveratrol 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 30384152-10 2019 Intriguingly, both resveratrol and JNK inhibitor SP600125 suppressed TNFalpha-induced IL6 and IL8 mRNA expression (P < 0.05). pyrazolanthrone 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 30521103-0 2019 Chondroitin sulfate inhibits secretion of TNF and CXCL8 from human mast cells stimulated by IL-33. Chondroitin Sulfates 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 30521103-5 2019 Preincubation with CS had no effect on MC degranulation stimulated by SP, but inhibited TNF (60%) and CXCL8 (45%) secretion from LAD2 cells stimulated by IL-33. Chondroitin Sulfates 19-21 C-X-C motif chemokine ligand 8 Homo sapiens 102-107 30521103-12 2019 The findings in this article show that CS inhibits secretion of TNF and CXCL8 from human cultured MC stimulated by IL-33. Chondroitin Sulfates 39-41 C-X-C motif chemokine ligand 8 Homo sapiens 72-77 31582650-4 2019 2FL reduced PM10-induced excess expression of interleukin (IL)-6, IL-8, IL-1alpha and IL-1beta in HaCaT keratinocytes. 2'-fucosyllactose 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 29874648-1 2019 This study investigated the effect of surfactants associated with sodium fluoride (NaF) on enamel erosion prevention, using an erosion-remineralization in vitro model. Sodium Fluoride 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 30520054-4 2019 Our results demonstrated that metformin significantly decreased the mRNA and protein levels of tumour necrosis factor-alpha (TNFalpha), interleukin (IL)-6, IL-8, and IL-1beta induced by TNFalpha. Metformin 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 30314969-7 2019 TSH significantly upregulated VEGF-A and CXCL8 expressions in BHP10-3SCp cells via AKT and ERK signaling, resulting in higher concentrations of VEGF-A and CXCL8 in conditioned medium of TSH-treated BHP10-3SCp cells (TSH-CM) compared with controls. Thyrotropin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 41-46 30314969-7 2019 TSH significantly upregulated VEGF-A and CXCL8 expressions in BHP10-3SCp cells via AKT and ERK signaling, resulting in higher concentrations of VEGF-A and CXCL8 in conditioned medium of TSH-treated BHP10-3SCp cells (TSH-CM) compared with controls. Thyrotropin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 155-160 30314969-7 2019 TSH significantly upregulated VEGF-A and CXCL8 expressions in BHP10-3SCp cells via AKT and ERK signaling, resulting in higher concentrations of VEGF-A and CXCL8 in conditioned medium of TSH-treated BHP10-3SCp cells (TSH-CM) compared with controls. Thyrotropin 186-189 C-X-C motif chemokine ligand 8 Homo sapiens 41-46 30314969-7 2019 TSH significantly upregulated VEGF-A and CXCL8 expressions in BHP10-3SCp cells via AKT and ERK signaling, resulting in higher concentrations of VEGF-A and CXCL8 in conditioned medium of TSH-treated BHP10-3SCp cells (TSH-CM) compared with controls. Thyrotropin 186-189 C-X-C motif chemokine ligand 8 Homo sapiens 155-160 30314969-8 2019 TSH-CM treatment enhanced tube formation potentials of endothelial cells, and blocking VEGF and/or CXCL8 reduced them. Thyrotropin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 30314969-9 2019 Blocking VEGF and/or CXCL8 also reduced TSH-dependent tumor growth with reduced tumor vasculature in vivo. Thyrotropin 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 21-26 29934049-8 2019 Analysis in vitro by MTT test and Boyden chamber assay showed exogenous IL-6 and IL-8 (a relatively short period of treatment with recombinant IL-6 or IL-8 equivalent to the autocrine levels) could significantly promote the proliferation of human osteoblastic, endothelial and monocytic cells, as well as the migration of human endothelial cells. monooxyethylene trimethylolpropane tristearate 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 30844798-9 2019 Chenodeoxycholic acid (CDCA) significantly decreased TEER, increased permeability, and increased interleukin-8 (IL-8) release from Caco-2 cells. Chenodeoxycholic Acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 30844798-9 2019 Chenodeoxycholic acid (CDCA) significantly decreased TEER, increased permeability, and increased interleukin-8 (IL-8) release from Caco-2 cells. Chenodeoxycholic Acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 30844798-9 2019 Chenodeoxycholic acid (CDCA) significantly decreased TEER, increased permeability, and increased interleukin-8 (IL-8) release from Caco-2 cells. Chenodeoxycholic Acid 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 30844798-9 2019 Chenodeoxycholic acid (CDCA) significantly decreased TEER, increased permeability, and increased interleukin-8 (IL-8) release from Caco-2 cells. Chenodeoxycholic Acid 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 30844798-10 2019 Pre-incubation with guggulsterone blocked CDCA-mediated IL-8 release; however, the decrease in TEER was not reversed. pregna-4,17-diene-3,16-dione 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 30844798-10 2019 Pre-incubation with guggulsterone blocked CDCA-mediated IL-8 release; however, the decrease in TEER was not reversed. Chenodeoxycholic Acid 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 30844798-11 2019 CDCA-induced IL-6 and IL-8 mRNA levels were blocked by guggulsterone. Chenodeoxycholic Acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 30844798-11 2019 CDCA-induced IL-6 and IL-8 mRNA levels were blocked by guggulsterone. pregna-4,17-diene-3,16-dione 55-68 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 30259626-7 2019 Studies with cell cultures of osteoblasts revealed in response to sodium fluoride (NaF) treatment, there was an induction of p16 hypermethylation and decreased expression, leading to increased cell proliferation, a longer S-phase of the cell cycle, and development of skeletal fluorosis. Sodium Fluoride 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 30259626-8 2019 Further, the methylation inhibitor, 5-aza-2-deoxycytidine, reversed the p16 hypermethylation and expression in response to NaF. Decitabine 36-57 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 30366059-5 2019 Induction of an inflammatory response was observed after LPS treatment and the addition of RESV led to decreases in expression of the inflammatory mediators, tumor necrosis factor-alpha (TNF-alpha), interleukin-8 (IL-8), and monocyte chemoattractant protein-1 (MCP-1), without cytotoxicity. Resveratrol 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 199-212 30366059-5 2019 Induction of an inflammatory response was observed after LPS treatment and the addition of RESV led to decreases in expression of the inflammatory mediators, tumor necrosis factor-alpha (TNF-alpha), interleukin-8 (IL-8), and monocyte chemoattractant protein-1 (MCP-1), without cytotoxicity. Resveratrol 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 30407866-6 2019 On the contrary, challenge with supraphysiological concentrations (10-25 mM), as might be used therapeutically, of propionate or butyrate in combination with TNFalpha resulted in substantially greater IL-6 and CXCL8 release from HLFs and ASM cells than challenge with TNFalpha alone, demonstrating synergistic effects. Butyrates 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 210-215 30257245-8 2019 Postradiotherapy treatment with different solutions (CHX, NaF, and EGCG) led to lower fluorescence intensity/mm2 in irradiated teeth than in the control group (distilled water; p < 0.05), as a result of MMP inactivation. Water 170-175 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 30651831-0 2019 Protective effects of astragaloside IV on IL-8-treated diaphragmatic muscle cells. astragaloside 22-35 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 30651831-4 2019 Diaphragmatic muscle cells extracted from neonatal rats were treated with a series of AS-IV concentrations (5, 10 or 20 mg/l) and the AKT inhibitor GSK690693 in the presence of interleukin-8 (IL-8). GSK690693 148-157 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 30651831-8 2019 IL-8 treatment resulted in decreased rates of cell proliferation and increased rates of AKT phosphorylation, cell apoptosis, caspase 3/9 activity, ROS production and proinflammatory factor production. Reactive Oxygen Species 147-150 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30651831-9 2019 AS-IV and GSK690693 treatment reversed the effects of IL-8. GSK690693 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 30777526-15 2019 Serum interleukin 8 levels were significantly higher in patients who received sevoflurane on postoperative days 1 (P = .045) and 7 (P = .037). Sevoflurane 78-89 C-X-C motif chemokine ligand 8 Homo sapiens 6-19 30777526-18 2019 CONCLUSIONS: Although sevoflurane seemed to produce higher interleukin 8 levels posttransplant, both desflurane and sevoflurane had similar effects on posttransplant kidney function. Sevoflurane 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 30957871-8 2019 RESULTS: Blocking of CD44H by anti-CD44H mAb on monocytes decreased the engulfment of TMVs and the secretion of CCL4 and CCL5, but had no effect on CCL2, CCL3 and CXCL8. cd44h 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 163-168 29929938-1 2019 BACKGROUND & PURPOSE: Recent studies suggested a role of prostaglandin E2 (PGE2) in the expression of the chemokine IL-8 by monocytes. Adenosine Monophosphate 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 29929938-1 2019 BACKGROUND & PURPOSE: Recent studies suggested a role of prostaglandin E2 (PGE2) in the expression of the chemokine IL-8 by monocytes. Dinoprostone 61-77 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 29929938-1 2019 BACKGROUND & PURPOSE: Recent studies suggested a role of prostaglandin E2 (PGE2) in the expression of the chemokine IL-8 by monocytes. Dinoprostone 79-83 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 29929938-4 2019 KEY RESULTS: In monocytic cell lines THP-1, MonoMac and U937 PGE2 had only a marginal impact on IL-8 induction but strongly enhanced TNFalpha-induced IL-8 mRNA and protein synthesis. Dinoprostone 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 29929938-4 2019 KEY RESULTS: In monocytic cell lines THP-1, MonoMac and U937 PGE2 had only a marginal impact on IL-8 induction but strongly enhanced TNFalpha-induced IL-8 mRNA and protein synthesis. Dinoprostone 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 30843005-1 2019 OBJECTIVE: We aimed to assess the feasibility of quantifying fluorine-18-fluorodexoglucose (18F-FDG) and 18F-sodium fluoride (18F-NaF) uptake in abdominal aorta and examine their association with age and cardiovascular risk factors. 18f-sodium fluoride 105-124 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 29929938-5 2019 Similarly, in PBMC IL-8 mRNA induction was larger by simultaneous stimulation with TNFalpha and PGE2 than by either stimulus alone. Dinoprostone 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 29929938-8 2019 In HEK293 cells expressing EP4, but not in wild type HEK293 cells lacking EP4, PGE2 enhanced TNFalpha-induced IL-8 protein and mRNA synthesis. Dinoprostone 79-83 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 29929938-9 2019 In THP-1 cells, the enhancement of TNFalpha-mediated IL-8 mRNA induction by PGE2 was mimicked by a PKA-activator. Dinoprostone 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 29929938-11 2019 PGE2 and TNFalpha synergistically activated transcription factor CREB, induced C/EBPss expression and enhanced the activity of an IL-8 promoter fragment containing -223 bp upstream of the transcription start site. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 29929938-12 2019 CONCLUSIONS AND IMPLICATIONS: These findings suggest that a combined stimulation of TNFalpha and PGE2/EP4 signal chains in monocytic cells leads to maximal IL-8 promoter activity, as well as IL-8 mRNA and protein induction, by activating the PKA/CREB/C/EBPss as well as NF-kappaB signal chains. Dinoprostone 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 29929938-12 2019 CONCLUSIONS AND IMPLICATIONS: These findings suggest that a combined stimulation of TNFalpha and PGE2/EP4 signal chains in monocytic cells leads to maximal IL-8 promoter activity, as well as IL-8 mRNA and protein induction, by activating the PKA/CREB/C/EBPss as well as NF-kappaB signal chains. Dinoprostone 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 29934049-4 2019 Here we demonstrated that in human osteoblastic MG-63, U2-OS and Saos-2 cells, besides VEGF, the other two pro-angiogenic factors IL-6 and IL-8 were also up-regulated by hypoxia and CoCl2 (a mimic of hypoxia). cobaltous chloride 182-187 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 30466028-6 2019 Moreover, linagliptin suppresses TNF-alpha-induced production of pro-inflammatory and pro-adhesive vascular cytokines including IL-6, IL-8, ICAM-1, and VCAM-1. Linagliptin 10-21 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 30471617-14 2019 In Mrgprx2 knockdown LAD2 cells, the effect of Quercetin (200 muM) reduced C48/80 induced calcium flux and the release of beta-hexosaminidase, histamine, MCP-1 and IL-8 compared with non-atopic control (NC) transfected LAD2 human mast cells, suggesting that Quercetin anti-pseudo-allergic effect was related to Mrgprx2. Quercetin 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 31146075-11 2019 In particular, 0.5 g of tungsten showed a significant rise of IL-6 which could also be found for IL-1beta and IL-8. Tungsten 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 30630560-10 2019 CONCLUSION: Compared with fentanyl combined anesthesia, the remifentanil combined anesthesia can significantly reduce serum levels of cytokines IL-8, IL-6, CRP, TNF- &alpha; and oxidative stress level, and is, therefore, more secure for patients undergoing laparoscopic surgery for colon cancer. Remifentanil 60-72 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 31560593-1 2019 Objective(s): The incorporation of Arginine (Arg) in NaF-containing child dentifrice might enhance its remineralizing potential, reducing fluorosis risk with significant anti-caries benefit. Arginine 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 31560593-1 2019 Objective(s): The incorporation of Arginine (Arg) in NaF-containing child dentifrice might enhance its remineralizing potential, reducing fluorosis risk with significant anti-caries benefit. Arginine 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 31560593-5 2019 Results: The percentage remineralization of the 2% Arg-NaF and 1100-ppm NaF groups was significantly higher than the 600-ppm NaF group (p<0.001). Arginine 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 31560593-7 2019 The EFU, Ca/P ratio, PO43- content of the 2% Arg-NaF group were significantly higher than the 600-ppm NaF group (p<0.01); while no significant difference was found between the 2% Arg-NaF and 1100-ppm NaF groups. Arginine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 31560593-8 2019 Conclusion: Within the limitations of the present study, incorporation of 2% arginine in 600-ppm NaF child formula dentifrice enhanced the remineralization potential of artificial enamel caries, to a level comparable to 1100-ppm NaF adult formula dentifrice. Arginine 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 97-100 30266621-9 2019 In vitro adsorption of AMI and Naf to the MD membrane was strong (RRvt,AMI = 4.4%, RRvt,Naf = 1.5%) but unspecific adsorption to cOFM was negligibly small (RRvt,AMI = 98% and RRvt,Naf = 98%). Amitriptyline 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 30056444-4 2019 PGN-induced secretion of inflammatory factors TNF-alpha and IL-8 in human SZ95 sebocytes was suppressed after knockdown of AhR and pretreatment with the AhR antagonist CH223191. 2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amide 168-176 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 30056444-5 2019 In addition, the AhR agonist 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) enhanced TNF-alpha and IL-8 secretion in PGN-pretreated sebocytes. Polychlorinated Dibenzodioxins 29-64 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 30056444-5 2019 In addition, the AhR agonist 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) enhanced TNF-alpha and IL-8 secretion in PGN-pretreated sebocytes. Polychlorinated Dibenzodioxins 66-70 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 30266621-9 2019 In vitro adsorption of AMI and Naf to the MD membrane was strong (RRvt,AMI = 4.4%, RRvt,Naf = 1.5%) but unspecific adsorption to cOFM was negligibly small (RRvt,AMI = 98% and RRvt,Naf = 98%). Amitriptyline 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 30507116-8 2018 The benzopyrene directionally led the bronchial epithelium to present observable cell shrinkage, cytoskeleton disintegration, Caspase-3 activation, overproduction of reactive oxygen species, and various inflammatory cytokine (TNF-alpha, IL-6, and IL-8) secretion, suggesting its significant inflammatory and cytotoxic effects on respiratory system. Benzopyrenes 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 30584842-9 2019 RESULTS: By FM, NAF-induced FI were higher in CZ than in surrounding skin (P <= 0.001). carzinophilin 46-48 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 30584842-10 2019 Highest NAF-FI were induced in skin pretreated with a thin CZ (CZ-20 microm), assessed by both FM and FCM and in particular, FI were higher than in skin pretreated with no CZ (CZ-0 microm) (FM P <= 0.041, FCM P < 0.012). carzinophilin 59-61 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 30584842-10 2019 Highest NAF-FI were induced in skin pretreated with a thin CZ (CZ-20 microm), assessed by both FM and FCM and in particular, FI were higher than in skin pretreated with no CZ (CZ-0 microm) (FM P <= 0.041, FCM P < 0.012). carzinophilin 63-65 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 30584842-10 2019 Highest NAF-FI were induced in skin pretreated with a thin CZ (CZ-20 microm), assessed by both FM and FCM and in particular, FI were higher than in skin pretreated with no CZ (CZ-0 microm) (FM P <= 0.041, FCM P < 0.012). Fosfomycin 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 30584842-10 2019 Highest NAF-FI were induced in skin pretreated with a thin CZ (CZ-20 microm), assessed by both FM and FCM and in particular, FI were higher than in skin pretreated with no CZ (CZ-0 microm) (FM P <= 0.041, FCM P < 0.012). carzinophilin 63-65 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 30584842-10 2019 Highest NAF-FI were induced in skin pretreated with a thin CZ (CZ-20 microm), assessed by both FM and FCM and in particular, FI were higher than in skin pretreated with no CZ (CZ-0 microm) (FM P <= 0.041, FCM P < 0.012). carzinophilin 63-65 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 30584842-10 2019 Highest NAF-FI were induced in skin pretreated with a thin CZ (CZ-20 microm), assessed by both FM and FCM and in particular, FI were higher than in skin pretreated with no CZ (CZ-0 microm) (FM P <= 0.041, FCM P < 0.012). Fosfomycin 208-211 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 30584842-13 2019 NAF-FI were higher than CAF-FI (P <= 0.036), and highest CAF-FI were induced by CZ-0 microm and CZ-20 microm compared to CZ-80 microm (P <= 0.009). cz-20 99-104 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 30315378-9 2019 Notably, vinpocetine increased TLR3 mRNA levels, as well as protein levels of the downstream signalling molecules TRIF-beta and IRF-3, and serum levels of the anti-inflammatory cytokines IL-10 and IL-8. vinpocetine 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 31418610-3 2019 Relapsed DME cases (T3) showed significantly higher levels of IL-6 (p = .028), IL-8 (p = .005), IP-10 (p = .013) and MCP-1 (p = .005) compared to T2.Conclusion: IP-10 and MCP-1 AH levels seem to be related to DEX intraocular action, decreasing after injection and increasing when DME relapses. dme 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 31418610-4 2019 In addition, IL-6 and IL-8 may play a role in DME late evolution and clinical relapse beyond DEX effect. dme 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 30445053-10 2019 In addition, pretreatment with PPT or DPN increased the expression of IL-8 in activated EoL-1 cells. 4,4',4''-(4-propyl-((1)H)-pyrazole-1,3,5-triyl) tris-phenol 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 30445053-10 2019 In addition, pretreatment with PPT or DPN increased the expression of IL-8 in activated EoL-1 cells. diarylpropionitrile 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 30598040-6 2018 DHS diminished interleukin-6 (IL-6) and interleukin-8 (IL-8) secretion but induced the significant upregulation of IL-8 mRNA associated with NF-kappaB and AP-1 activation. Silybin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 30598040-6 2018 DHS diminished interleukin-6 (IL-6) and interleukin-8 (IL-8) secretion but induced the significant upregulation of IL-8 mRNA associated with NF-kappaB and AP-1 activation. Silybin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 30598040-6 2018 DHS diminished interleukin-6 (IL-6) and interleukin-8 (IL-8) secretion but induced the significant upregulation of IL-8 mRNA associated with NF-kappaB and AP-1 activation. Silybin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 30420215-2 2019 Fluorine-18 (18F)-sodium fluoride (NaF) PET similarly portrays osteoblastic activity but with improved spatial and contrast resolution and more accurate anatomic localization. fluorine-18 (18f)-sodium fluoride 0-33 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 30252571-11 2019 The concentration of IL-8 and IL-10 were decreased in patients with half and standard-dose ticagrelor group. Ticagrelor 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 30665751-0 2019 Clinical usefulness of two-phase 18F-sodium-fluoride (18F-NaF) bone PET/CT for evaluating treatment response of bone metastases from breast cancer: Case report. 18f-sodium-fluoride 33-52 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 30665751-1 2019 We report the case of a breast cancer patient in whom a two-phase 18F-sodium-fluoride (18F-NaF) bone PET/CT was useful for detecting hidden bone metastases and assessing treatment response. 18f-sodium-fluoride 66-85 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 30622945-10 2018 Moreover, PL induced an early and transient increase of the pro-inflammatory response triggered by IL-1alpha, by inducing COX-2 expression and secretion of a large amount of PGE2, IL-6, and IL-8. pl 10-12 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 30582047-1 2018 The separation and recovery of NaF from fluorine containing solution by the common ion effect of Na+ was studied. Fluorine 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 30323026-5 2019 Suppression of IL-8 in human embryonic kidney (HEK293) cells that were transformed to express TLR5 was observed not only upon inflammatory stimulation by flagellin but also in response to tumor necrosis factor alpha (TNF-alpha) and phorbol myristate acetate (PMA), despite the fact that the TNF-alpha- and PMA-induced inflammatory pathways reportedly are not TLR5 mediated. Tetradecanoylphorbol Acetate 232-257 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 30323026-5 2019 Suppression of IL-8 in human embryonic kidney (HEK293) cells that were transformed to express TLR5 was observed not only upon inflammatory stimulation by flagellin but also in response to tumor necrosis factor alpha (TNF-alpha) and phorbol myristate acetate (PMA), despite the fact that the TNF-alpha- and PMA-induced inflammatory pathways reportedly are not TLR5 mediated. Tetradecanoylphorbol Acetate 259-262 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 30323026-5 2019 Suppression of IL-8 in human embryonic kidney (HEK293) cells that were transformed to express TLR5 was observed not only upon inflammatory stimulation by flagellin but also in response to tumor necrosis factor alpha (TNF-alpha) and phorbol myristate acetate (PMA), despite the fact that the TNF-alpha- and PMA-induced inflammatory pathways reportedly are not TLR5 mediated. Tetradecanoylphorbol Acetate 306-309 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 30582047-3 2018 It was found that when the compound containing sodium, such as Na2CO3 or Na2SO4 was added into NaF saturated solution to product the common ion effect of Na+, most of the NaF can be crystallized without evaporating concentration, and the added Na2CO3 or Na2SO4 can be recovered by cooling crystallization. sodium carbonate 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 30582047-3 2018 It was found that when the compound containing sodium, such as Na2CO3 or Na2SO4 was added into NaF saturated solution to product the common ion effect of Na+, most of the NaF can be crystallized without evaporating concentration, and the added Na2CO3 or Na2SO4 can be recovered by cooling crystallization. sodium sulfate 73-79 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 30582047-3 2018 It was found that when the compound containing sodium, such as Na2CO3 or Na2SO4 was added into NaF saturated solution to product the common ion effect of Na+, most of the NaF can be crystallized without evaporating concentration, and the added Na2CO3 or Na2SO4 can be recovered by cooling crystallization. sodium sulfate 73-79 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 30582047-3 2018 It was found that when the compound containing sodium, such as Na2CO3 or Na2SO4 was added into NaF saturated solution to product the common ion effect of Na+, most of the NaF can be crystallized without evaporating concentration, and the added Na2CO3 or Na2SO4 can be recovered by cooling crystallization. sodium carbonate 244-250 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 30582047-3 2018 It was found that when the compound containing sodium, such as Na2CO3 or Na2SO4 was added into NaF saturated solution to product the common ion effect of Na+, most of the NaF can be crystallized without evaporating concentration, and the added Na2CO3 or Na2SO4 can be recovered by cooling crystallization. sodium sulfate 254-260 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 30582047-4 2018 Combining cooling crystallization with the common ion effect of Na+, different processes can be designed to recover NaF from different fluorine containing solutions. Fluorine 135-143 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 30582047-2 2018 The solubility of NaF in the solutions of NaCl, NaNO3, Na2CO3, Na2SO4 and NaOH at 30 C was determined. Sodium Chloride 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 30582047-2 2018 The solubility of NaF in the solutions of NaCl, NaNO3, Na2CO3, Na2SO4 and NaOH at 30 C was determined. sodium nitrate 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 30582047-2 2018 The solubility of NaF in the solutions of NaCl, NaNO3, Na2CO3, Na2SO4 and NaOH at 30 C was determined. sodium carbonate 55-61 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 30582047-2 2018 The solubility of NaF in the solutions of NaCl, NaNO3, Na2CO3, Na2SO4 and NaOH at 30 C was determined. sodium sulfate 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 30582047-2 2018 The solubility of NaF in the solutions of NaCl, NaNO3, Na2CO3, Na2SO4 and NaOH at 30 C was determined. Sodium Hydroxide 74-78 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 30582047-3 2018 It was found that when the compound containing sodium, such as Na2CO3 or Na2SO4 was added into NaF saturated solution to product the common ion effect of Na+, most of the NaF can be crystallized without evaporating concentration, and the added Na2CO3 or Na2SO4 can be recovered by cooling crystallization. Sodium 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 30582047-3 2018 It was found that when the compound containing sodium, such as Na2CO3 or Na2SO4 was added into NaF saturated solution to product the common ion effect of Na+, most of the NaF can be crystallized without evaporating concentration, and the added Na2CO3 or Na2SO4 can be recovered by cooling crystallization. Sodium 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 30582047-3 2018 It was found that when the compound containing sodium, such as Na2CO3 or Na2SO4 was added into NaF saturated solution to product the common ion effect of Na+, most of the NaF can be crystallized without evaporating concentration, and the added Na2CO3 or Na2SO4 can be recovered by cooling crystallization. sodium carbonate 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 30273544-11 2018 Collectively, our data showed that HDAC6 mediated upregulation of IL-8 can regulate the Dox sensitivity of OS cells via transcriptionally regulating the expression of ABCB1. Doxorubicin 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 30547786-15 2018 TNFalpha treatment elicited strong induction of the chemokine CXCL8, the kinases MAP3K8, MAP4K4 and negative regulators of cytokine signaling, i.e. SOCS2&SOCS3. Adenosine Monophosphate 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 30651923-8 2018 Dynamic upward variations were also observed with respect to IL-8 levels in sunitinib-refractory individuals: 28.5 pg/mL at baseline vs. 38.3 pg/mL at 3 months, p-value=0.024. Sunitinib 76-85 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 31458330-6 2018 It is deduced that the new phases of AlNi, NaF, and KH that were formed in situ during the dehydrogenation process are the key factors for the improvement of dehydrogenation properties of NaAlH4. sodium aluminum hydride 188-194 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 30273544-0 2018 Histone deacetylase 6 regulated expression of IL-8 is involved in the doxorubicin (Dox) resistance of osteosarcoma cells via modulating ABCB1 transcription. Doxorubicin 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 30273544-12 2018 Targeted inhibition of IL-8 might be a potent potential approach for overcome the Dox resistance of OS cells and helpful for clinical therapy of OS patients. Doxorubicin 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 30273544-0 2018 Histone deacetylase 6 regulated expression of IL-8 is involved in the doxorubicin (Dox) resistance of osteosarcoma cells via modulating ABCB1 transcription. Doxorubicin 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 30273544-3 2018 The expression of IL-8, while not VEGFA, IL-32, or IL-34, was significantly increased in OS/Dox cells as compared with that in the parental cells. Doxorubicin 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 30426751-4 2018 Pretreatment of intestinal Caco-2 cells with resveratrol suppressed the TNF-alpha-induced production of IL-8 (control 1.00 +- 0.04, TNFalpha 3.40 +- 0.16, TNFalpha+Res 1.81 +- 0.28 AU, p < 0.05) and phosphorylation of the inflammatory signaling molecules including NF-kappaB, extracellular signal-regulated kinase and stress c-Jun N-terminal protein kinase. Resveratrol 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 30178199-3 2018 In this retrospective study, we aimed to assess the uptake of the bone-specific PET radiotracer, F-18 fluoride (NaF), in primary breast cancers to determine its sensitivity and to identify any differences in NaF uptake between calcified and non-calcified tumors, histological subtypes, and patients with or without axillary lymphadenopathy. f-18 fluoride 97-110 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 30518116-0 2018 Chlorogenic Acid (CGA) Isomers Alleviate Interleukin 8 (IL-8) Production in Caco-2 Cells by Decreasing Phosphorylation of p38 and Increasing Cell Integrity. Chlorogenic Acid 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 41-54 30518116-0 2018 Chlorogenic Acid (CGA) Isomers Alleviate Interleukin 8 (IL-8) Production in Caco-2 Cells by Decreasing Phosphorylation of p38 and Increasing Cell Integrity. Chlorogenic Acid 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 30518116-0 2018 Chlorogenic Acid (CGA) Isomers Alleviate Interleukin 8 (IL-8) Production in Caco-2 Cells by Decreasing Phosphorylation of p38 and Increasing Cell Integrity. Chlorogenic Acid 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 41-54 30518116-0 2018 Chlorogenic Acid (CGA) Isomers Alleviate Interleukin 8 (IL-8) Production in Caco-2 Cells by Decreasing Phosphorylation of p38 and Increasing Cell Integrity. Chlorogenic Acid 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 30273544-4 2018 IL-8 neutralization antibody can significantly increase the Dox sensitivity of OS/Dox cells. Doxorubicin 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30273544-4 2018 IL-8 neutralization antibody can significantly increase the Dox sensitivity of OS/Dox cells. Doxorubicin 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30563042-4 2018 H2O2 at low concentrations can trigger a transient anti-inflammatory adiponectin secretion and reduced gene expression of toll-like receptors (TLRs) in PBMCs but may act as a stimulator of proinflammatory genes (IL6, IL8) and mitochondrial dynamics-related proteins (Mtf2, NRF2, Tfam). Hydrogen Peroxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 217-220 30178199-5 2018 F-18 fluoride uptake as maximum standardized uptake value (NaF SUVmax) was measured in the primary tumor, enlarged axillary lymph nodes and contralateral normal/non-tumoral breast tissue. Fluorides 5-13 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 29457379-8 2018 Subjects with urate deposits had higher IL-6 (257.2 versus 47.0 pg/ml; P = 0.005), IL-8 (73.2 versus 12.0 pg/ml; P = 0.026), and miR-155 (0.21 versus 0.16; P = 0.015) levels than those without deposition findings. Uric Acid 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 30372880-10 2018 Furthermore, in vitro studies demonstrated that AJE inhibits TNF-alpha-induced IL-8, IL-1beta, and COX-2 expression in human intestinal epithelial HT-29 cells and tert-butyl hydroperoxide-induced reduction of ZO-1 and occludin expression in human intestinal epithelial Caco-2 cells. aje 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 29457379-9 2018 CONCLUSION: In individuals with chronic asymptomatic hyperuricemia, the presence of synovitis and double contour sign by US may represent a subclinical manifestation of monosodium urate crystal nucleation, capable of triggering inflammatory pathways (IL-6 and IL-8) and mechanisms of intercellular communication (miR-155), similar to what is observed in patients with gout. Uric Acid 169-185 C-X-C motif chemokine ligand 8 Homo sapiens 260-264 30372883-6 2018 Vildagliptin potently suppresses high glucose-induced generation of reactive oxygen species (ROS) and production of vascular inflammatory factors including tumor necrosis factor-alpha (TNF-alpha), interleukin-8 (IL-8), intercellular cell adhesion molecule-1 (ICAM-1) and monocyte chemotactic protein 1 (MCP-1). Vildagliptin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 197-210 30372883-6 2018 Vildagliptin potently suppresses high glucose-induced generation of reactive oxygen species (ROS) and production of vascular inflammatory factors including tumor necrosis factor-alpha (TNF-alpha), interleukin-8 (IL-8), intercellular cell adhesion molecule-1 (ICAM-1) and monocyte chemotactic protein 1 (MCP-1). Vildagliptin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 30372883-6 2018 Vildagliptin potently suppresses high glucose-induced generation of reactive oxygen species (ROS) and production of vascular inflammatory factors including tumor necrosis factor-alpha (TNF-alpha), interleukin-8 (IL-8), intercellular cell adhesion molecule-1 (ICAM-1) and monocyte chemotactic protein 1 (MCP-1). Glucose 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 30134219-15 2018 Both curcumin-loaded liposomes formulation (1 mug/mL, 5 mug/mL) resulted in significant (p < 0.05) reduction in the level of pro-inflammatory marker expression such as IL-6, IL-8, IL-1beta and TNF-a compared to positive control group. Curcumin 5-13 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 30325822-5 2018 Although previous publications have reported F-NaF uptake portraying calcification in soft tissue, these findings demonstrate a new domain in which to assess calcium metabolism using F-NaF PET/CT. Calcium 158-165 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 30276439-0 2018 NaF uptake in unstable plaque: what does fluoride uptake mean? Fluorides 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 30482611-6 2018 The crystallization reaction was performed by incubating hydroxyapatite powder with NaF or SDF for 48h. Durapatite 57-71 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 30591798-7 2018 The results from RT-PCR analysis revealed a significant reduction in the expression of genes involved in inflammation including, HMGB1, IL-6 and IL-8 on treatment of DU-145 cells with crocetin. crocetin 184-192 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 30513776-9 2018 Serum IL-8 level was positively correlated with CC status, weight loss, sarcopenia, but was negatively correlated with total psoas area (TPA). Tetradecanoylphorbol Acetate 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 30221352-11 2018 Sr2+ reversed LPS-stimulated proinflammatory cytokine expressions such as tumor necrosis factor alpha, interleukin (IL)-1beta, IL-6 and IL-8. strontium cation 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 30111198-7 2018 Several studies have shown intriguing pharmacologic effects associated with curcumin, which inhibits NF-kappaB expression by regulating NF-kappaB/IkB pathway and down-regulation expression of pro-inflammatory cytokines, such as Interleukin (IL)-1, IL-6, IL-8, and tumor necrosis factor (TNF)-alpha. Curcumin 76-84 C-X-C motif chemokine ligand 8 Homo sapiens 254-258 30153075-2 2018 Recently, we found that verbascoside, the major component in the sweet olive ethanolic extract (OFE), inhibited IL-8 secretion in human colorectal adenocarcinoma WiDr cells. acteoside 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 30153075-5 2018 In the IL-8 secretion assay, both OFE (100 mug/mL) and verbascoside (10 muM) significantly inhibited IL-8 production in WiDr cells. acteoside 55-67 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 30153075-5 2018 In the IL-8 secretion assay, both OFE (100 mug/mL) and verbascoside (10 muM) significantly inhibited IL-8 production in WiDr cells. acteoside 55-67 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 30360960-7 2018 AlaGln supplementation also reduced peritoneal protein loss, increased ex vivo stimulated tumor necrosis factor (TNF)-alpha release, and reduced systemic IL-8 levels. alanylglutamine 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 29941296-8 2018 RESULTS: Those patients who were randomly assigned to risperidone had higher levels of IL-8 (p = 0.000) and MIP-1beta (p = 0.007) than healthy volunteers at baseline, whereas no differences were found between patients initially assigned to aripiprazole and healthy volunteers. Risperidone 54-65 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 30012425-6 2018 Blocking interaction between hCXCL8 and tsCXCR1/2 with allosteric antagonists (reparixin and SB265610) significantly decreased tree shrew PBMC transmigration. reparixin 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 29-35 30130557-3 2018 Using Sprague-Dawley rats developmentally exposed to sodium fluoride (NaF) from pregnancy until 6 months of delivery as in vivo model, we showed that fluoride impaired the cognitive abilities of offspring rats, decreased the density of dendritic spines and the expression of synapse proteins synaptophysin (SYN) and postsynaptic density protein-95 (PSD-95) in hippocampus, suggesting fluoride-induced cognitive deficit associates with synaptic impairment. Sodium Fluoride 53-68 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 30130557-3 2018 Using Sprague-Dawley rats developmentally exposed to sodium fluoride (NaF) from pregnancy until 6 months of delivery as in vivo model, we showed that fluoride impaired the cognitive abilities of offspring rats, decreased the density of dendritic spines and the expression of synapse proteins synaptophysin (SYN) and postsynaptic density protein-95 (PSD-95) in hippocampus, suggesting fluoride-induced cognitive deficit associates with synaptic impairment. Fluorides 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 30130557-3 2018 Using Sprague-Dawley rats developmentally exposed to sodium fluoride (NaF) from pregnancy until 6 months of delivery as in vivo model, we showed that fluoride impaired the cognitive abilities of offspring rats, decreased the density of dendritic spines and the expression of synapse proteins synaptophysin (SYN) and postsynaptic density protein-95 (PSD-95) in hippocampus, suggesting fluoride-induced cognitive deficit associates with synaptic impairment. Fluorides 150-158 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 30130557-6 2018 Importantly, fluoride treatment increased phospho-extracellular signal-regulated kinases 1 and 2 (p-ERK1/2) expression, while inhibition of p-ERK1/2 significantly attenuated the effects of NaF, indicating a regulating role of p-ERK1/2 in BDNF-TrkB signaling disruption. Fluorides 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 189-192 30012425-6 2018 Blocking interaction between hCXCL8 and tsCXCR1/2 with allosteric antagonists (reparixin and SB265610) significantly decreased tree shrew PBMC transmigration. 1-(2-bromophenyl)-3-(7-cyano-3H-benzotriazol-4-yl)urea 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 29-35 30546347-9 2018 Conclusion: Overall, our findings demonstrated that infertile women with PCOS, who were candidate for IVF benefited from chromium supplementation for 8 weeks in terms of lowering hs-CRP and improving gene expression of PPAR-gamma, GLUT-1, LDLR, and IL-1, though chromium had no effect on the gene expression of IL-8, TNF-alpha, TGF-beta, and VEGF. Chromium 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 311-315 30485517-10 2018 The production of inflammatory cytokines, including tumor necrosis factor alpha, interleukin (IL)- 6, and IL-8, was reduced by carvacrol in LPS-induced RA-FLSs. carvacrol 127-136 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 30456862-5 2018 A water-soluble fraction of urban dust (UD-WS) induces pro-inflammatory cytokine release (IL-8) from NHEKs (measured via ELISA). Water 2-7 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 30456862-5 2018 A water-soluble fraction of urban dust (UD-WS) induces pro-inflammatory cytokine release (IL-8) from NHEKs (measured via ELISA). ud-ws 40-45 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 30456862-7 2018 RESULTS: In vitro studies using NHEKs demonstrate SIG-1273 protects against urban dust-induced cell toxicity, reducing cell death by 66% and concentration dependently inhibits UD-WS-induced IL-8 production (IC50 = 20 nmol/L), outperforming niacinamide, ascorbic acid, and alpha-tocopherol, commonly used actives in antipollution skin-care products. ud-ws 176-181 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 30646653-7 2018 Conclusion: Macrophages and IL-8 may play an important role in the pathogenesis of airway inflammation after long-term inhalation of iron and its compounds, the airway function in patients of occupational pulmonary thesaurosis was found damaged. Iron 133-137 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 30359018-4 2018 Moreover, in the presence of NaF, a ligand exchange was observed by NMR spectroscopy in hafnocene diiodide (Cp2HfI2) to afford hafnocene difluoride (Cp2HfF2). cp2hff2 149-156 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 30466990-0 2018 Orientin inhibits invasion by suppressing MMP-9 and IL-8 expression via the PKCalpha/ ERK/AP-1/STAT3-mediated signaling pathways in TPA-treated MCF-7 breast cancer cells. Tetradecanoylphorbol Acetate 132-135 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 30442959-10 2018 tRF5-AlaCGC activates p65, subsequently leading to enhanced secretion of IL-8 in arsenite response. arsenite 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 30359018-3 2018 For a catalytic reductive coupling, the addition of sodium fluoride (NaF) to the reaction system is required. Sodium Fluoride 52-67 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 30359018-4 2018 Moreover, in the presence of NaF, a ligand exchange was observed by NMR spectroscopy in hafnocene diiodide (Cp2HfI2) to afford hafnocene difluoride (Cp2HfF2). hafnocene diiodide 88-106 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 30359018-4 2018 Moreover, in the presence of NaF, a ligand exchange was observed by NMR spectroscopy in hafnocene diiodide (Cp2HfI2) to afford hafnocene difluoride (Cp2HfF2). cp2hfi2 108-115 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 30359018-4 2018 Moreover, in the presence of NaF, a ligand exchange was observed by NMR spectroscopy in hafnocene diiodide (Cp2HfI2) to afford hafnocene difluoride (Cp2HfF2). hafnocene difluoride 127-147 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 30466991-0 2018 Berberine down-regulates IL-8 expression through inhibition of the EGFR/MEK/ERK pathway in triple-negative breast cancer cells. Berberine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 30466990-9 2018 CONCLUSION: Orientin inhibits migratory and invasive responses by suppressing MMP-9 and IL-8 expression through mitigation of TPA-induced PKCalpha and ERK activation, as well as the nuclear translocation of AP-1 and STAT3. Tetradecanoylphorbol Acetate 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 30336048-6 2018 Measurements on micron-sized hematite particles terminated by the charged and amphoteric (012) and the relatively uncharged (001) faces point to the formation of salt loadings of similar composition to those of cryosalts of NaCl, NaBr, NaI, and NaF. Salts 162-166 C-X-C motif chemokine ligand 8 Homo sapiens 245-248 30466991-2 2018 PURPOSE: Here, we investigated the regulatory mechanism of IL-8 expression as well as the pharmacological effect of berberine (BBR) on IL-8 expression in triple-negative breast cancer (TNBC) cells. Berberine 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 30466991-2 2018 PURPOSE: Here, we investigated the regulatory mechanism of IL-8 expression as well as the pharmacological effect of berberine (BBR) on IL-8 expression in triple-negative breast cancer (TNBC) cells. Berberine 127-130 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 30466991-10 2018 These IL-8 levels were decreased by EGFR (Neratinib and Afatinib) and MEK (PD98059) inhibitors in TNBC cells. neratinib 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 30466991-10 2018 These IL-8 levels were decreased by EGFR (Neratinib and Afatinib) and MEK (PD98059) inhibitors in TNBC cells. Afatinib 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 30466991-10 2018 These IL-8 levels were decreased by EGFR (Neratinib and Afatinib) and MEK (PD98059) inhibitors in TNBC cells. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 30429487-6 2018 In addition, a single intra-discal injection of NTG-101 into the injured IVD-NPs resulted in sustained expression of healthy extra-cellular matrix (ECM) proteins (aggrecan, collagen 2A1) and reduced expression of inflammation associated proteins and molecules (IL-1beta, IL-6, IL-8, MMP-13, Cox-2 and PGE2) as compared to vehicle controls. ntg-101 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 277-281 30255322-0 2018 Molecular recognition of IL-8, IL-10, IL-12, and IL-15 in biological fluids using phthalocyanine-based stochastic sensors. phthalocyanine 82-96 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 30400326-4 2018 Exposing monocytes to CaP-CHI-HA resulted in a secretion of pro-healing VEGF and TGF-beta growth factors, TNF-alpha, MCP-1, IL-6 and IL-8 pro-inflammatory mediators but also IL-10 anti-inflammatory cytokine along with an inflammatory index below 1.5 (versus 2.5 and 7.5 following CaP and LPS stimulation, respectively). cap 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 30295964-4 2018 RESULTS: Poly (I:C) induced the expression of the interferon-stimulated genes (ISG) MxA, OAS2 and APOBEC3G, and the cytokines MCP-1, IL-8, IL-6, CCL20, IFNbeta and RANTES by fibroblasts from all three sites. Poly I-C 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 30390648-6 2018 RESULTS: Challenge with the omega-6 PUFA arachidonic acid (AA), but not omega-3 PUFAs or SFAs, resulted in increased IL-6 and CXCL8 release from fibroblasts, however IL-6 and CXCL8 release was reduced in COPD (n = 19) compared to non-COPD (n = 36). omega-6 pufa 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 126-131 30390648-6 2018 RESULTS: Challenge with the omega-6 PUFA arachidonic acid (AA), but not omega-3 PUFAs or SFAs, resulted in increased IL-6 and CXCL8 release from fibroblasts, however IL-6 and CXCL8 release was reduced in COPD (n = 19) compared to non-COPD (n = 36). omega-6 pufa 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 175-180 30390648-6 2018 RESULTS: Challenge with the omega-6 PUFA arachidonic acid (AA), but not omega-3 PUFAs or SFAs, resulted in increased IL-6 and CXCL8 release from fibroblasts, however IL-6 and CXCL8 release was reduced in COPD (n = 19) compared to non-COPD (n = 36). Arachidonic Acid 41-57 C-X-C motif chemokine ligand 8 Homo sapiens 126-131 30390648-6 2018 RESULTS: Challenge with the omega-6 PUFA arachidonic acid (AA), but not omega-3 PUFAs or SFAs, resulted in increased IL-6 and CXCL8 release from fibroblasts, however IL-6 and CXCL8 release was reduced in COPD (n = 19) compared to non-COPD (n = 36). Arachidonic Acid 41-57 C-X-C motif chemokine ligand 8 Homo sapiens 175-180 30175447-10 2018 RESULTS: Excess glucose triggered a trophoblast sterile inflammatory IL-8 and antimigratory response through HMGB1 activation of TLR4. Glucose 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 30019285-0 2018 Technical feasibility, radiation dosimetry and clinical use of 18F-sodium fluoride (NaF) in evaluation of metastatic bone disease in pediatric population. 18f-sodium fluoride 63-82 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 30019285-1 2018 PURPOSE: The role of 18F-fluoride (18F-NaF) PET-CT for the detection of bone metastases in adults is well established and is considered superior to conventional bone scintigraphy. Fluoride ion f-18 21-33 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 30255322-1 2018 Two stochastic sensors based on the modification of graphite paste with the complexes formed by phthalocyanine (PhCN) with Ni and Cu were designed and used for molecular recognition of IL-8, IL-10, IL-12, and IL-15. Graphite 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 30255322-1 2018 Two stochastic sensors based on the modification of graphite paste with the complexes formed by phthalocyanine (PhCN) with Ni and Cu were designed and used for molecular recognition of IL-8, IL-10, IL-12, and IL-15. phthalocyanine 96-110 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 30255322-1 2018 Two stochastic sensors based on the modification of graphite paste with the complexes formed by phthalocyanine (PhCN) with Ni and Cu were designed and used for molecular recognition of IL-8, IL-10, IL-12, and IL-15. phthalocyanine 112-116 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 30255322-1 2018 Two stochastic sensors based on the modification of graphite paste with the complexes formed by phthalocyanine (PhCN) with Ni and Cu were designed and used for molecular recognition of IL-8, IL-10, IL-12, and IL-15. Copper 130-132 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 30175388-6 2018 In THP-1 derived macrophages, AOH (1-20 microM) was found to suppress lipopolysaccharide (LPS)-induced NF-kappaB pathway activation, decrease secretion of the proinflammatory cytokines IL-8, IL-6, TNF-alpha and to induce secretion of the anti-inflammatory IL-10. alternariol 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 30774881-4 2019 Through an experimental and computational approach using fluorescence polarization, ITC, docking and molecular dynamics simulations we investigate the binding of these functionalized GAG derivatives to ten representative regulatory proteins including IL-8, IL-10, BMP-2, sclerostin, TIMP-3, CXCL-12, TGF-beta, FGF-1, FGF-2, and AT-III, and we establish structure-activity relationships for GAG recognition. Glycosaminoglycans 183-186 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 30178114-0 2018 Changes in plasma interleukin-8 and tumor necrosis factor-alpha levels during the early treatment period as a predictor of the response to sorafenib in patients with unresectable hepatocellular carcinoma. Sorafenib 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 30178114-9 2018 CONCLUSIONS: Changes in plasma interleukin-8 and TNF-alpha levels during the first few days could predict the response to sorafenib therapy in HCC patients. Sorafenib 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 30193010-1 2018 In an initial screening, the dichloromethane extract from the leaves of Melodorum fruticosum showed distinct inhibitory effects on the release of interleukin-8 (IL-8) in human neutrophils. Methylene Chloride 29-44 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 30193010-5 2018 Three constituents, melodamide A, 2",4"-dihydroxy-4,6"-dimethoxychalcone, and 2",6"-dihydroxy-4"-methoxychalcone, showed significant inhibition of IL-8 release (IC50 =6.6, 8.6, and 11.6 mum, respectively) and TNF-alpha production (IC50 =4.5, 13.3, and 6.2 mum, respectively). melodamide A 20-32 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 30014900-4 2018 Our results demonstrate that PCCVC but not Calbuco ash particles induce cytotoxicity on human conjunctival epithelial cells viewed as a decrease in cell proliferation and the transmembrane mucin MUC1 expression; a pro-inflammatory response mediated by IL-6 and IL-8; and an imbalance of the redox environment leading to protein oxidative damage. pccvc 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 261-265 30193010-5 2018 Three constituents, melodamide A, 2",4"-dihydroxy-4,6"-dimethoxychalcone, and 2",6"-dihydroxy-4"-methoxychalcone, showed significant inhibition of IL-8 release (IC50 =6.6, 8.6, and 11.6 mum, respectively) and TNF-alpha production (IC50 =4.5, 13.3, and 6.2 mum, respectively). 2",4"-dihydroxy-4,6"-dimethoxychalcone 34-72 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 30193010-5 2018 Three constituents, melodamide A, 2",4"-dihydroxy-4,6"-dimethoxychalcone, and 2",6"-dihydroxy-4"-methoxychalcone, showed significant inhibition of IL-8 release (IC50 =6.6, 8.6, and 11.6 mum, respectively) and TNF-alpha production (IC50 =4.5, 13.3, and 6.2 mum, respectively). 2',6'-dihydroxy-4'-methoxychalcone 78-112 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 30179909-1 2018 F-fluoride (F-NaF) uptake in soft tissue metastases of medullary thyroid carcinoma (MTC) has been reported. f-fluoride 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 30133131-8 2018 These results indicate that mLU8C-PU inhibits migratory and invasive responses in MCF-7 breast cancer cells by suppressing MMP-9 and IL-8 expression through mitigating TPA-induced PKCalpha, JNK activation, and the nuclear translocation of AP-1 and NF-kappaB. mlu8c-pu 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 30133131-8 2018 These results indicate that mLU8C-PU inhibits migratory and invasive responses in MCF-7 breast cancer cells by suppressing MMP-9 and IL-8 expression through mitigating TPA-induced PKCalpha, JNK activation, and the nuclear translocation of AP-1 and NF-kappaB. Tetradecanoylphorbol Acetate 168-171 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 30783327-0 2018 Sulfated polysaccharides of seagrass Halophila ovalis suppresses tumor necrosis factor-alpha-induced chemokine interleukin-8 secretion in HT-29 cell line. Polysaccharides 9-24 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 30171271-1 2018 OBJECTIVES: The aim of this study was to evaluate the 18F-sodium fluoride (18F-NaF) coronary uptake compared to coronary intravascular ultrasound (IVUS) in patients with symptomatic coronary artery disease. 18f-sodium fluoride 54-73 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 30171271-2 2018 BACKGROUND: 18F-NaF PET enables the assessment of vascular osteogenesis by interaction with surface hydroxyapatite, while IVUS enables both identification and quantification of intra-plaque components. Durapatite 100-114 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 30125599-0 2018 IL-8 analogue CXCL8 (3-72) K11R/G31P, modulates LPS-induced inflammation via AKT1-NF-kbeta and ERK1/2-AP-1 pathways in THP-1 monocytes. g31p 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30125599-0 2018 IL-8 analogue CXCL8 (3-72) K11R/G31P, modulates LPS-induced inflammation via AKT1-NF-kbeta and ERK1/2-AP-1 pathways in THP-1 monocytes. g31p 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 30125599-2 2018 Its antagonist, CXCL8 (3-72) K11R/G31P (G31P), represses inflammatory reactions via competitive binding to CXC chemokine family, preferentially G protein-couple receptors (GPCRs) CXCR1/2. g31p 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 16-21 30125599-4 2018 LPS (1 microg/ml) induced elevation of IL-8 was significantly reduced by G31P (20 microg/ml and 30 microg/ml), with relatively increased inhibition of CXCR2 than CXCR1. g31p 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 30125599-10 2018 Collectively, the IL-8 analogue, G31P, modulates the inflammatory profile of LPS induced inflammation in THP-1 monocytes via AKT1-NF-kbeta and ERK1/2-AP-1 pathways. g31p 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 30783327-6 2018 CONCLUSION: Overall, the results presented in this study suggest that purified fraction Ho FrIV of Ho-SP could suppress the TNF-alpha-induced secretion of IL-8 in HT-29 and thus could be used as a promising antioxidant and anti-inflammatory candidate with potential benefits. spiropyran 99-104 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 30114464-5 2018 r-SP potently induced interleukin (IL)-6 and IL-8 at both mRNA and protein levels in a dose- and time-dependent manner, whereas h-SP and f-SP poorly induced them. r-sp 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 29964032-5 2018 Vaccination of mice with CAMP factor considerably reduced the growth of P. acnes and production of MIP-2, a murine counterpart of human IL-8. Cyclic AMP 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 29964032-8 2018 Incubation of ex vivo acne explants with monoclonal antibodies to CAMP factor markedly attenuated the amounts of IL-8 and IL-1beta. Cyclic AMP 66-70 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 30276549-11 2018 ELISA analysis showed that aspirin significantly decreased the production of inflammatory cytokines IFN-gamma (p value < 0.05) and IL-8 (p value < 0.001) in PE-DMSCs. Aspirin 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 30276549-11 2018 ELISA analysis showed that aspirin significantly decreased the production of inflammatory cytokines IFN-gamma (p value < 0.05) and IL-8 (p value < 0.001) in PE-DMSCs. dmscs 166-171 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 30114464-6 2018 Of note, the mRNA levels of IL-6 and IL-8 were approximately two-fold higher when cells were stimulated with 3 x 107 CFU/ml of r-SP for 3 h, while the protein levels of IL-6 and IL-8 were approximately five-fold higher after stimulation with 3 x 107 CFU/ml of r-SP for 24 h. Furthermore, r-SP exhibited potent activation of Toll-like receptor 2 compared with h-SP or f-SP. f-sp 367-371 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 30610810-1 2018 PURPOSE: Acute monocytic leukemia remains a big challenge, and there are a series of non-specific esterases which can be inhibited by sodium fluoride (NaF) in mononuclear cells, providing insights into the leukemia targeted therapy. Sodium Fluoride 134-149 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 30610810-5 2018 The 3-(4, 5-dimethylthiazol-2-yl)-2), 5-diphenyltetrazolium bromide (MTT) assay was used to detect the antitumor effect of NaF on THP-1 cells in vitro. thiazolyl blue 4-67 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 30610810-9 2018 After 24hrs of exposure to NaF at greater than 1mmol/L, typical apoptotic changes were observed, accompanied by the alpha-NAE positive reaction and decreased intensity. alpha-nae 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 30610810-13 2018 CONCLUSION: NaF inhibited the proliferation of THP-1 cells and the activation of alpha-NAE by adversely regulating the expression of Bax and Bcl-2. alpha-nae 81-90 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 31099333-6 2018 Quantitative results of RT-PCR demonstrated that magnesium supplementation downregulated gene expression levels of interleukin-8 (IL-8) (P = 0.03) and tumor necrosis factor-alpha (TNF-alpha) (P = 0.006) and upregulated gene expression levels of transforming growth factor beta (TGF-beta) (P = 0.03) in PBMCs of women with GDM, compared with placebo. Magnesium 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 31099333-6 2018 Quantitative results of RT-PCR demonstrated that magnesium supplementation downregulated gene expression levels of interleukin-8 (IL-8) (P = 0.03) and tumor necrosis factor-alpha (TNF-alpha) (P = 0.006) and upregulated gene expression levels of transforming growth factor beta (TGF-beta) (P = 0.03) in PBMCs of women with GDM, compared with placebo. Magnesium 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 31099333-9 2018 Overall, magnesium supplementation for six weeks significantly decreased gene expression levels of IL-8 and TNF-alpha, and increased TGF-beta in women with GDM. Magnesium 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 30114464-7 2018 The expression of IL-6 and IL-8 induced by r-SP was mediated through the activation of mitogen-activated protein kinases. r-sp 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 30114464-9 2018 Taken together, we suggest that r-SP stimulates the human respiratory epithelial cells to produce the cytokines IL-6 and IL-8, which might influence the induction of adaptive immune responses. r-sp 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 30114464-6 2018 Of note, the mRNA levels of IL-6 and IL-8 were approximately two-fold higher when cells were stimulated with 3 x 107 CFU/ml of r-SP for 3 h, while the protein levels of IL-6 and IL-8 were approximately five-fold higher after stimulation with 3 x 107 CFU/ml of r-SP for 24 h. Furthermore, r-SP exhibited potent activation of Toll-like receptor 2 compared with h-SP or f-SP. r-sp 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 30114464-6 2018 Of note, the mRNA levels of IL-6 and IL-8 were approximately two-fold higher when cells were stimulated with 3 x 107 CFU/ml of r-SP for 3 h, while the protein levels of IL-6 and IL-8 were approximately five-fold higher after stimulation with 3 x 107 CFU/ml of r-SP for 24 h. Furthermore, r-SP exhibited potent activation of Toll-like receptor 2 compared with h-SP or f-SP. r-sp 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 30114464-6 2018 Of note, the mRNA levels of IL-6 and IL-8 were approximately two-fold higher when cells were stimulated with 3 x 107 CFU/ml of r-SP for 3 h, while the protein levels of IL-6 and IL-8 were approximately five-fold higher after stimulation with 3 x 107 CFU/ml of r-SP for 24 h. Furthermore, r-SP exhibited potent activation of Toll-like receptor 2 compared with h-SP or f-SP. r-sp 260-264 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 30114464-6 2018 Of note, the mRNA levels of IL-6 and IL-8 were approximately two-fold higher when cells were stimulated with 3 x 107 CFU/ml of r-SP for 3 h, while the protein levels of IL-6 and IL-8 were approximately five-fold higher after stimulation with 3 x 107 CFU/ml of r-SP for 24 h. Furthermore, r-SP exhibited potent activation of Toll-like receptor 2 compared with h-SP or f-SP. r-sp 260-264 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 30114464-6 2018 Of note, the mRNA levels of IL-6 and IL-8 were approximately two-fold higher when cells were stimulated with 3 x 107 CFU/ml of r-SP for 3 h, while the protein levels of IL-6 and IL-8 were approximately five-fold higher after stimulation with 3 x 107 CFU/ml of r-SP for 24 h. Furthermore, r-SP exhibited potent activation of Toll-like receptor 2 compared with h-SP or f-SP. h-sp 359-363 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 30373224-3 2018 It was found that only NaF + HCl solution was effective for synthesizing highly pure V2C MXene. v2c mxene 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 30630805-1 2018 Present investigation is conducted to investigate the clinical efficacy of mesalazine in combination with the Bifid Triple Viable Capsules on the ulcerative colitis (UC) and the resultant effect on the inflammatory factors (TNF-alpha, IL-8 and IL-10) of UC patients. Mesalamine 75-85 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 30322479-5 2018 This review highlights the use of 18F-sodium fluoride (NaF) with PET (NaF-PET), NaF-PET/CT, or NaF-PET/MRI in the evaluation of osteoporosis and osteopenia in the lumbar spine and hip. 18f-sodium fluoride 34-53 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 30384436-4 2018 Here, using backbone 15N-relaxation nuclear magnetic resonance (NMR) data, we characterized the dynamic properties of the CXCL8 monomer and the CXCR1 N-domain in the free and bound states. 15n 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 30261438-6 2018 Polarized T84 monolayers responded to apically applied C3a with increased CXCL8 mRNA more rapidly than if the C3a was applied basolaterally. T84 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 74-79 30376894-8 2018 The mAb from clone KH4-8 effectively inhibited increases in interleukin-6 (IL-6) and IL-8 expression in recombinant adiponectin-stimulated human osteoblasts and human umbilical vein endothelial cells. kh4-8 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 30230320-0 2018 Distinct Differences in Structural States of Conserved Histidines in Two Related Proteins: NMR Studies of the Chemokines CXCL1 and CXCL8 in the Free Form and Macromolecular Complexes. Histidine 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 131-136 30259744-9 2018 diCQA isomers were relatively more effective at reducing IL-8 ( p < 0.05). dicqa 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 30405600-8 2018 Intestinal crypts cultured with supernatants from BI119-treated commensal-specific CD4+ T cells showed decreased expression of CXCL1, CXCL8 and CCL20. bi119 50-55 C-X-C motif chemokine ligand 8 Homo sapiens 134-139 30405600-10 2018 BI119 has a more profound effect in ileal CD with additional significant downregulation of IL23R, CSF2, CXCL1, CXCL8, and S100A8, and upregulation of DEFA5. bi119 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 111-116 30230320-3 2018 Here, we characterized the structural features of histidines in the chemokines CXCL8 and CXCL1 in the free, GAG heparin-bound, and CXCR2 receptor N-terminal domain-bound states using solution NMR spectroscopy. Histidine 50-60 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 30230320-3 2018 Here, we characterized the structural features of histidines in the chemokines CXCL8 and CXCL1 in the free, GAG heparin-bound, and CXCR2 receptor N-terminal domain-bound states using solution NMR spectroscopy. gag heparin 108-119 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 30230320-4 2018 CXCL8 and CXCL1 share two conserved histidines, one in the N-loop and the other in the 30s loop. Histidine 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 30546959-7 2019 Mechanistically, MALAT1 recruited Brahma-related gene 1 (BRG1), a catalytic subunit of chromatin remodeling complex switching/sucrose non-fermentable (SWI/SNF), to the promoter region of IL-6 and CXCL8, and thus facilitated NF-kappaB to induce the expression of these inflammatory factors. Sucrose 126-133 C-X-C motif chemokine ligand 8 Homo sapiens 196-201 30230320-5 2018 In CXCL8, both histidines exist in the Nepsilon2 tautomeric state in the free, GAG-bound, and receptor-bound forms. Histidine 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 3-8 30230320-5 2018 In CXCL8, both histidines exist in the Nepsilon2 tautomeric state in the free, GAG-bound, and receptor-bound forms. Glycosaminoglycans 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 3-8 30314357-3 2018 At IC50, 2-AmPh caused decrease in nuclear content of NF-kappaB p65 polypeptide and mRNA expression of NF-kappaB target genes encoding interleukin-8 and anti-apoptotic protein BIRC3. 2-amph 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 135-148 30014946-0 2018 A highly selective electrochemical immunosensor based on conductive carbon black and star PGMA polymer composite material for IL-8 biomarker detection in human serum and saliva. Polymers 95-102 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 30014946-2 2018 In this study, we developed an electrochemical IL 8 biosensor by modification with a conductive composite including Super P, polyvinylidene fluoride (PVDF) and star polymer (SPGMA) of disposable ITO electrode surface. polyvinylidene fluoride 125-148 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 30014946-2 2018 In this study, we developed an electrochemical IL 8 biosensor by modification with a conductive composite including Super P, polyvinylidene fluoride (PVDF) and star polymer (SPGMA) of disposable ITO electrode surface. polyvinylidene fluoride 150-154 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 30014946-4 2018 Anti-IL 8 antibodies were utilized as biorecognition molecules and bound to epoxy groups of star polymer covalently. star polymer 92-104 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 30014946-9 2018 Super P-star polymer composite modified immunosensor was easy, sensitive, cheap and reliable analytical method for IL 8 detection. Polymers 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 30402038-7 2018 Lonafarnib significantly suppressed LPS-, IL-1beta-, or TNF-alpha-induced IL-6, IL-8, MCP-1, and GRO-alpha expression and secretion in placental tissue. lonafarnib 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30333797-9 2018 CPA patients did not differ significantly in the BALF cytokine profile compared to patients with respiratory disorders without CPA, but showed significant higher values for IFN-gamma, IL-1b, IL-6, IL-8, and TNF-alpha compared to healthy individuals. cpa 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 30199234-10 2018 After addition of TNF-alpha to the monolayer, two compounds (butyrate and gallic acid) suppressed IL-8 production, suggesting their potential anti-inflammatory effects, whereas the dietary factor forskolin significantly increased IL-8 production. Gallic Acid 74-85 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 30199234-10 2018 After addition of TNF-alpha to the monolayer, two compounds (butyrate and gallic acid) suppressed IL-8 production, suggesting their potential anti-inflammatory effects, whereas the dietary factor forskolin significantly increased IL-8 production. Colforsin 196-205 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 30199234-10 2018 After addition of TNF-alpha to the monolayer, two compounds (butyrate and gallic acid) suppressed IL-8 production, suggesting their potential anti-inflammatory effects, whereas the dietary factor forskolin significantly increased IL-8 production. Butyrates 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 30194878-9 2018 RESULTS: Compared to excess glucose alone, combination excess glucose and low-dose aPL (a) further augmented trophoblast inflammatory IL-1beta, inflammasome-associated uric acid and caspase-1, and pro-angiogenic PlGF; (b) dampened trophoblast inflammatory IL-8, anti-angiogenic sEndoglin, and sFlt-1; and (c) further reduced trophoblast migration. Glucose 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 30390734-37 2018 Nicotinamide can inhibit cytokine release (IL-1, IL-6, IL-8, and TNF-alpha) from immune cells, inhibit chemotaxis and degranulation of immune cells, inhibit lymphocyte blast transformation, and suppress T-cell activity (6). Niacinamide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 29435831-2 2018 With the exception of the control group, human umbilical vein endothelial cells (HUVECs) were treated with sodium fluoride (NaF) (1.2 mug/mL) for 24 h, with or without a 2-h pretreatment with 100 nM insulin-like growth factor 1 (IGF-1, a PI3K/AKT agonist), or 10 muM histamine (HIS, a eNOS agonist). Sodium Fluoride 107-122 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 29800615-9 2018 Levels of inflammatory cytokines IL-8, IL-10, IL-6, TNFR2, INF-alpha, and INF-beta were reduced after ruxolitinib treatment. ruxolitinib 102-113 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 30022772-0 2018 TRPV4 Channel-Regulated ATP Release Contributes to gamma-Irradiation-Induced Production of IL-6 and IL-8 in Epidermal Keratinocytes. Adenosine Triphosphate 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 30022772-5 2018 HaCaT cells treated with TRPV4 channel agonist GSK1016790A also showed increased IL-6 and IL-8 production. N-(1-((4-(2-(((2,4-dichlorophenyl)sulfonyl)amino)-3-hydroxypropanoyl)-1-piperazinyl)carbonyl)-3-methylbutyl)-1-benzothiophene-2-carboxamide 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 30022772-6 2018 In both cases, IL-6/IL-8 production was not increased at 24 h after stimulation, but was increased at 48 h. ATP was released from cells exposed to gamma-irradiation or TRPV4 channel agonist, and the release was suppressed by TRPV4 channel inhibitors. Adenosine Triphosphate 108-111 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 30022772-7 2018 The gamma-irradiation-induced increase in IL-6 and IL-8 production was suppressed by apyrase (ecto-nucleotidase), NF157 (selective P2Y11 receptor antagonist) and SB203580 (p38 MAPK inhibitor). SB 203580 162-170 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 30022772-9 2018 Our results suggest that gamma-irradiation of keratinocytes induces ATP release via activation of the TRPV4 channel, and then ATP activates P2Y11 receptor and p38 MAPK-NF-kappaB signaling, resulting in IL-6/IL-8 production. Adenosine Triphosphate 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 30119218-6 2018 The presence of loratadine in endothelial culture efficiently suppressed ox-LDL-induced attachment of monocytes to endothelial cells, production of ROS and vascular adhesion molecules, and induction cytokines including VCAM-1, E-selectin, TNF-alpha, IL-6 and IL-8. Loratadine 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 30119221-4 2018 Results showed that treatment with prunetin (10, 30, and 50 muM) inhibited lipopolysaccharide (LPS)-induced expression and secretion of interleukin (IL)-6, IL-8, and mucin 5 AC (MUC5 AC) in RPMI2650 cells, and attenuated the effect of LPS on toll-like receptor 4 (TLR4) and myeloid differentiation primary response 88 (MyD88) expression. prunetin 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 30119221-5 2018 TAK-242 (an inhibitor of TLR4) treatment or TLR4 knockdown attenuated LPS-induced expression and secretion of IL-6, IL-8 and MUC5 AC. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 29435831-4 2018 The levels of NO significantly decreased in all experimental groups; however, the levels of NO were obviously higher in the NaF + HIS and NaF + IGF-1 groups, compared to the NaF group. Histamine 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 29435831-5 2018 The p-eNOS/eNOS ratios dropped clearly in NaF and NaF + HIS groups, while that in the NaF + HIS group was distinctly higher than that in the NaF group. Histamine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 29435831-5 2018 The p-eNOS/eNOS ratios dropped clearly in NaF and NaF + HIS groups, while that in the NaF + HIS group was distinctly higher than that in the NaF group. Histamine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 29435831-5 2018 The p-eNOS/eNOS ratios dropped clearly in NaF and NaF + HIS groups, while that in the NaF + HIS group was distinctly higher than that in the NaF group. Histamine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 30059431-0 2018 Targeted Therapy With Anaplastic Lymphoma Kinase Inhibitor (Alectinib) in Adolescent Metastatic Non-Small Cell Lung Carcinoma: 18F-NaF PET/CT in Response Evaluation. alectinib 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 29934223-3 2018 OMVs from both EHEC O157:H7 and sorbitol-fermenting (SF) EHEC O157:H- induced production of interleukin-8 (IL-8) in Caco-2, HCT-8, and HT-29 intestinal epithelial cell lines. Sorbitol 32-40 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 29951871-5 2018 The results showed that taraxasterol not only reduced the production of TNF-alpha, IL-8, PGE2, and NO induced by LPS, but also reduced the expression of iNOS and COX-2. taraxasterol 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 29951871-8 2018 The inhibition of taraxasterol on TNF-alpha, IL-8, PGE2, and NO production can be reversed by geranylgeranyl diphosphate (GGPP, the LXRalpha inhibitor). taraxasterol 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 29951871-8 2018 The inhibition of taraxasterol on TNF-alpha, IL-8, PGE2, and NO production can be reversed by geranylgeranyl diphosphate (GGPP, the LXRalpha inhibitor). geranylgeranyl pyrophosphate 94-120 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 29951871-8 2018 The inhibition of taraxasterol on TNF-alpha, IL-8, PGE2, and NO production can be reversed by geranylgeranyl diphosphate (GGPP, the LXRalpha inhibitor). geranylgeranyl pyrophosphate 122-126 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 29983334-5 2018 Here, we show that primary human monocytes stimulated with Shiga toxin 1a (Stx1a) through the glycolipid receptor globotriaosylceramide released larger amounts of proinflammatory molecules (IL-1beta, TNFalpha, IL-6, G-CSF, CXCL8, CCL2, CCL4) than Stx1a-treated neutrophils. globotriaosylceramide 114-135 C-X-C motif chemokine ligand 8 Homo sapiens 223-228 30015917-8 2018 Overall, the present results suggested that wogonin inhibited the 5-LO/BLT2/ERK/IL-8/MMP-9 signaling cascade and demonstrated that this cascade may be an important target through which wogonin exerts its anticancer effects in breast cancer. wogonin 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30102465-7 2018 PA, but not OA, enhances the production of IL-6 and IL-8 in response to TNF-alpha. Palmitic Acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 28852897-1 2018 PURPOSE: In this study, we elucidated the effects of berberine, a major alkaloid component contained in medicinal herbs, such as Phellodendri Cortex and Coptidis Rhizoma, on expression of monocyte chemotactic protein-1 (MCP-1) and interleukin-8 (IL-8) in a human retinal pigment epithelial cell line (ARPE-19) caused by lipopolysaccharide (LPS) stimulation. Berberine 53-62 C-X-C motif chemokine ligand 8 Homo sapiens 231-244 28852897-1 2018 PURPOSE: In this study, we elucidated the effects of berberine, a major alkaloid component contained in medicinal herbs, such as Phellodendri Cortex and Coptidis Rhizoma, on expression of monocyte chemotactic protein-1 (MCP-1) and interleukin-8 (IL-8) in a human retinal pigment epithelial cell line (ARPE-19) caused by lipopolysaccharide (LPS) stimulation. Berberine 53-62 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 28852897-7 2018 CONCLUSIONS: These findings indicate that berberine inhibited the expression of MCP-1 and IL-8 induced by LPS. Berberine 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 29030990-6 2018 Moreover, nanohydrogel of quercetin was able to reduce significantly IL-8, IL-6, and VEGF production in pro-inflammatory conditions with interesting implications on the mechanism of glioblastoma cells drug resistance. Quercetin 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 30203575-7 2018 RESULTS: In the substance P-induced inflammation model, 2% diosmin cream exhibited significant vasoconstrictive (proportion of dilated capillaries: -29%, capillary luminal area: -49% vs no cream + stress) and anti-inflammatory (IL-8 release: -36% vs no cream + stress) effects. Diosmin 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 228-232 28176254-2 2018 18Fluorine-labeled sodium fluoride (18F-NaF) is a widely available radioisotope and PET imaging allows for absolute quantification of tracer uptake. Fluorine-18 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 28176254-2 2018 18Fluorine-labeled sodium fluoride (18F-NaF) is a widely available radioisotope and PET imaging allows for absolute quantification of tracer uptake. Sodium Fluoride 19-34 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 30100024-14 2018 RESULTS: Simvastatin reduced TLR4-induced ICAM-1, IL-8, and MCP-1 expression in AVICs. Simvastatin 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 29992525-6 2018 In particular, 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) has shown promise in the detection of both high-risk atherosclerotic plaque features and vascular calcification activity, which predicts future development of new vascular calcium deposits. 18f-sodium fluoride 15-34 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 29992525-6 2018 In particular, 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) has shown promise in the detection of both high-risk atherosclerotic plaque features and vascular calcification activity, which predicts future development of new vascular calcium deposits. Calcium 252-259 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 29882686-10 2018 ZnO and CuO nanoparticles displayed severe cytotoxicity and enhanced gene expression of heme oxygenase-1 (HO-1) and interleukin-8 (IL-8). Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 30217257-8 2018 RESULTS: Honokiol significantly decreased pro-inflammatory cytokine (IL1A, IL6) and chemokine (CXCL8, CXCL1, CCL2) mRNA expression and secretion from fetal membranes (amnion and choriodecidua) and myometrium stimulated with LPS, fsl-1 or poly(I:C). honokiol 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 30217943-9 2018 The levels of TNF-alpha, IL-8, CC16, and ICAM-1 in EBC were significantly lower, and SOD activity was higher, at T2 in the NAC group; similar data were found in serum at T2, T3, and T4. Acetylcysteine 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 30033171-1 2018 The aim of this work was to investigate the complex phenomena underlying the adsorption of an anti-human IL-8 (anti-IL8) monoclonal antibody (mAb) to m-aminophenylboronate (m-APBA) by Flow Microcalorimetry (FMC) and to understand the role of non-specific interactions in the adsorption process. m-aminophenylboronate 150-171 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 30033171-1 2018 The aim of this work was to investigate the complex phenomena underlying the adsorption of an anti-human IL-8 (anti-IL8) monoclonal antibody (mAb) to m-aminophenylboronate (m-APBA) by Flow Microcalorimetry (FMC) and to understand the role of non-specific interactions in the adsorption process. m-aminophenylboronate 150-171 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 30033171-1 2018 The aim of this work was to investigate the complex phenomena underlying the adsorption of an anti-human IL-8 (anti-IL8) monoclonal antibody (mAb) to m-aminophenylboronate (m-APBA) by Flow Microcalorimetry (FMC) and to understand the role of non-specific interactions in the adsorption process. m-apba 173-179 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 30033171-1 2018 The aim of this work was to investigate the complex phenomena underlying the adsorption of an anti-human IL-8 (anti-IL8) monoclonal antibody (mAb) to m-aminophenylboronate (m-APBA) by Flow Microcalorimetry (FMC) and to understand the role of non-specific interactions in the adsorption process. m-apba 173-179 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 30033171-3 2018 Results showed that the adsorption of anti-IL8 mAb to m-APBA is enthalpically driven (DeltaHads<0), as expected for the predominant reversible esterification reaction between boronates and cis-diols-containing molecules. deltahads 86-95 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 30033171-3 2018 Results showed that the adsorption of anti-IL8 mAb to m-APBA is enthalpically driven (DeltaHads<0), as expected for the predominant reversible esterification reaction between boronates and cis-diols-containing molecules. boronates 178-187 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 30033171-3 2018 Results showed that the adsorption of anti-IL8 mAb to m-APBA is enthalpically driven (DeltaHads<0), as expected for the predominant reversible esterification reaction between boronates and cis-diols-containing molecules. cis-diols 192-201 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 30266096-8 2018 RESULTS: Ingenol mebutat significantly and dose-dependently induced the expression of proinflammatory chemokines (CXCL8, CCL2) and AMP (RNase7, HBD3) in HEK and epithelial cancer cell lines. ingenol 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 114-119 30261896-11 2018 In the CSF, methylprednisolone enhanced the interleukin-8 release (p < 0.001) but did not affect postoperative changes in CSF levels of tumor necrosis factor alpha. Methylprednisolone 12-30 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 30086077-1 2018 OBJECTIVE: The aim of this study was to describe osseous metabolic activity with respect to age and weight in the spine as expressed through fluorine-18-sodium fluoride (F-NaF) uptake in a healthy male population. fluorine-18-sodium fluoride 141-168 C-X-C motif chemokine ligand 8 Homo sapiens 172-175 30219183-1 2018 18F-sodium fluoride (18F-NaF) PET/CT provides high sensitivity and specificity for the assessment of bone and joint diseases. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 30505227-1 2018 The use of F-18 sodium fluoride (NaF) positron emission tomography/computed tomography (PET/CT) bone scan is increasing because of its higher sensitivity and specificity over standard bone scintigraphy (BS). Fluorine-18 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 30505227-1 2018 The use of F-18 sodium fluoride (NaF) positron emission tomography/computed tomography (PET/CT) bone scan is increasing because of its higher sensitivity and specificity over standard bone scintigraphy (BS). Sodium Fluoride 16-31 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 30486522-3 2018 The mechanism is mainly by inhibiting the activation of nuclear factor (NF-kappaB), mitogen-activated protein kinase (MAPKs) and signal transducers and activators of transcription (STAT) signaling pathways and down-regulating the inflammatory gene expression including tumor necrosis factor-alpha (TNF-alpha), prostaglandin E2 (PGE2), nitric oxide (NO), interleukin-1(IL-1), IL-6, IL-8 and other inflammatory factors. Dinoprostone 310-326 C-X-C motif chemokine ligand 8 Homo sapiens 381-385 30486522-3 2018 The mechanism is mainly by inhibiting the activation of nuclear factor (NF-kappaB), mitogen-activated protein kinase (MAPKs) and signal transducers and activators of transcription (STAT) signaling pathways and down-regulating the inflammatory gene expression including tumor necrosis factor-alpha (TNF-alpha), prostaglandin E2 (PGE2), nitric oxide (NO), interleukin-1(IL-1), IL-6, IL-8 and other inflammatory factors. Dinoprostone 328-332 C-X-C motif chemokine ligand 8 Homo sapiens 381-385 30486522-3 2018 The mechanism is mainly by inhibiting the activation of nuclear factor (NF-kappaB), mitogen-activated protein kinase (MAPKs) and signal transducers and activators of transcription (STAT) signaling pathways and down-regulating the inflammatory gene expression including tumor necrosis factor-alpha (TNF-alpha), prostaglandin E2 (PGE2), nitric oxide (NO), interleukin-1(IL-1), IL-6, IL-8 and other inflammatory factors. Nitric Oxide 335-347 C-X-C motif chemokine ligand 8 Homo sapiens 381-385 29882686-10 2018 ZnO and CuO nanoparticles displayed severe cytotoxicity and enhanced gene expression of heme oxygenase-1 (HO-1) and interleukin-8 (IL-8). Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 29882686-11 2018 The IL-8 gene expression was also increased from Bi2O3 exposure. bi2o3 49-54 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 29882686-14 2018 The enhancement of HO-1, IL-8, and MT2A gene expressions was related to the cytotoxic activity of metal oxide nanoparticles. metal oxide 98-109 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 30236152-8 2018 In contrast, DEX was the strongest inhibitor of IL-6, IL-8, and tissue-destructive enzymes in RASF. Dexamethasone 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 30236078-2 2018 The purpose of this study is to assess the role of 18F-Sodium fluoride (18F-NaF) positron emission tomography-computed tomography (PET/CT) bone scans in evaluating patients with limited ankle range of motion (ROM) after trauma. 18f-sodium fluoride 51-70 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 29402343-10 2018 The increased phosphorylations of PI3K, AKT, and mTOR, and the upregulation of CXCL8 induced by miR-204 suppression were all abolished by the addition of LY294002 and AZD8055 (inhibitors of PI3K/AKT and mTOR, respectively). 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 154-162 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 30188700-0 2018 Cell Motility Facilitated by Mono(2-ethylhexyl) Phthalate via Activation of the AKT-beta-Catenin-IL-8 Axis in Colorectal Cancer. mono-(2-ethylhexyl)phthalate 29-57 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 30188700-6 2018 Our results showed that treatment with MEHP enriched the population of cancer-stem-cell (CSC)-like cells and upregulated IL-8 expression by inducing the AKT-beta-catenin-TCF4 signaling pathway. mono-(2-ethylhexyl)phthalate 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 30188700-7 2018 Blocking beta-catenin-TCF4-mediated IL-8 expression reversed the MEHP-induced migration and enrichment of CSC-like cells. mono-(2-ethylhexyl)phthalate 65-69 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 29402343-10 2018 The increased phosphorylations of PI3K, AKT, and mTOR, and the upregulation of CXCL8 induced by miR-204 suppression were all abolished by the addition of LY294002 and AZD8055 (inhibitors of PI3K/AKT and mTOR, respectively). (5-(2,4-bis((3S)-3-methylmorpholin-4-yl)pyrido(2,3-d)pyrimidin-7-yl)-2-methoxyphenyl)methanol 167-174 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 30258441-1 2018 The glutamic acid-leucine-arginine (ELR) motif is a hallmark feature shared by mammalian inflammatory CXC chemokines such the granulocyte chemo-attractant CXCL8 (interleukin-8, IL-8). glutamic acid-leucine-arginine 4-34 C-X-C motif chemokine ligand 8 Homo sapiens 155-160 30223511-2 2018 The aim of this paper was to investigate the influence of Dentin Caries-like Lesions (DCLL)-Producing Model on microtensile bond strength (muTBS) of etch and rinse adhesive systems and investigate the effect of remineralizing agents such as Sodium Fluoride (NaF), MI Paste (MP) and Curodont Repair (CR) on caries-affected dentin (n = 6). dcll 86-90 C-X-C motif chemokine ligand 8 Homo sapiens 258-261 30258441-1 2018 The glutamic acid-leucine-arginine (ELR) motif is a hallmark feature shared by mammalian inflammatory CXC chemokines such the granulocyte chemo-attractant CXCL8 (interleukin-8, IL-8). glutamic acid-leucine-arginine 4-34 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 30258441-1 2018 The glutamic acid-leucine-arginine (ELR) motif is a hallmark feature shared by mammalian inflammatory CXC chemokines such the granulocyte chemo-attractant CXCL8 (interleukin-8, IL-8). glutamic acid-leucine-arginine 4-34 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 30258441-1 2018 The glutamic acid-leucine-arginine (ELR) motif is a hallmark feature shared by mammalian inflammatory CXC chemokines such the granulocyte chemo-attractant CXCL8 (interleukin-8, IL-8). elr 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 155-160 30258441-1 2018 The glutamic acid-leucine-arginine (ELR) motif is a hallmark feature shared by mammalian inflammatory CXC chemokines such the granulocyte chemo-attractant CXCL8 (interleukin-8, IL-8). elr 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 30258441-1 2018 The glutamic acid-leucine-arginine (ELR) motif is a hallmark feature shared by mammalian inflammatory CXC chemokines such the granulocyte chemo-attractant CXCL8 (interleukin-8, IL-8). elr 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 30205620-7 2018 PE concentrations of ENA-78/VEGF/IL-8/MDC/PCS/indoxyl sulphate correlate with serum creatinine concentrations. Creatinine 84-94 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 30204781-9 2018 CONCLUSIONS: The IL-8 concentration in the aqueous humor was associated with responsiveness to IVB in DME patients. dme 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 30254551-8 2018 The sensitivity, specificity, and agreement rate of 18F-NaF PET/CT for detecting bone metastatic lesions were 98.3%, 65.7%, and 92.9%, respectively; these values were 42.9%, 97.1%, and 51.9%, respectively, for 18F-FDG PET/CT. Fluorine-18 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 30233225-8 2018 Results: Dextran sulfate strongly and significantly inhibited PMA-induced PGE2 production, inhibited KLK5 and MMP-9 mRNA expression, and IL-8, IL-1alpha and VEGF production, and displayed a highly significant inhibitory effect on VEGF-induced pseudotube formation. Dextran Sulfate 9-24 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 30233225-9 2018 In SP-stimulated human skin explants, HMC significantly decreased the proportion of dilated vessels, total vessel area, and IL-8 production. TFF2 protein, human 3-5 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 29758106-9 2018 Among all subjects, sputum H2 S levels showed a trend to decrease with FEV1 %predicted and significantly positive correlations with sputum neutrophils (%), sputum IL-8 and serum IL-8. Deuterium 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 30193323-9 2018 Treatment with idelalisib inhibited the IL-1beta-induced expression of IL-6 and IL-8. idelalisib 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30254686-7 2018 As a result, ALE showed significant antioxidant activities and inhibited the production of reactive oxygen species (ROS), matrix metalloproteinases (MMPs), and interleukin-8 (IL-8) as well as suppressed mitogen-activated proteins kinases (MAPKs) such as extracellular signal regulated kinases (ERK), c-Jun N terminal kinases (JNK), and p38 MAPK triggered by heat shock treatment in human dermal fibroblasts (HDFs). Epinephrine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 160-173 30254686-7 2018 As a result, ALE showed significant antioxidant activities and inhibited the production of reactive oxygen species (ROS), matrix metalloproteinases (MMPs), and interleukin-8 (IL-8) as well as suppressed mitogen-activated proteins kinases (MAPKs) such as extracellular signal regulated kinases (ERK), c-Jun N terminal kinases (JNK), and p38 MAPK triggered by heat shock treatment in human dermal fibroblasts (HDFs). Epinephrine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 29758106-9 2018 Among all subjects, sputum H2 S levels showed a trend to decrease with FEV1 %predicted and significantly positive correlations with sputum neutrophils (%), sputum IL-8 and serum IL-8. Deuterium 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 29524267-0 2018 Cytokine patterns in vitro, in particular IL-5/IL-8 ratio, to detect patients with nickel contact allergy. Nickel 83-89 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 30411727-4 2018 SUBJECTS AND METHODS: This study was part of the cardiovascular molecular calcification assessed by 18F-sodium fluoride (NaF) (CAMONA) PET/computed tomography (CT) study. Sodium Fluoride 104-119 C-X-C motif chemokine ligand 8 Homo sapiens 121-124 29931171-9 2018 Stimulation of primary trophoblasts with palmitate led to increased mRNA expression and protein release of the cytokine IL6 and the chemokine IL8. Palmitates 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 30080191-1 2018 F-sodium fluoride (NaF) is a bone-seeking agent that can also localize extraosseous calcifying lesions. f-sodium fluoride 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 29990693-8 2018 Furthermore, the levels of inflammatory factors IL-1beta, IFN-gamma and TNF-alpha were decreased after CXCL8-IP10, dexamethasone or ceftazidime treatment. Ceftazidime 132-143 C-X-C motif chemokine ligand 8 Homo sapiens 103-108 30015877-6 2018 Furthermore, RA inhibited the production of pro-angiogenic factors, including matrix metalloproteinase (MMP)-9, pentraxin-3, interleukin-8, VEGF and placental growth factor under normoxic and hypoxic conditions, and suppressed the phorbol 12-myristate 13-acetate-induced increase in the gelatinolytic MMP-9 activity and MMP-9 expression in HT1080 cells. rhapontin 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 125-138 30175192-7 2018 Imiquimod-induced expression of interleukin (IL)-6, IL-8, and vascular endothelial growth factor (VEGF) was inhibited by TLR7 siRNA in HIOEC cells as determined by reverse transcription polymerase chain reaction (RT-PCR). Imiquimod 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 30025786-5 2018 RESULTS: While IP-10 levels were significantly reduced in TB+ subjects in all the sub-groups, IL-8 levels were significantly reduced in NDM-TB+ and increased in KDM-TB+ subjects. Terbium 140-142 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 30015902-5 2018 Pretreatment with spilanthol decreased TNF-alpha-induced COX-2 expression by western blotting and suppressed the expression of pro-inflammatory mediators, including interleukin (IL)-6, IL-8 and monocyte chemotactic protein 1 using ELISA. N-isobutyl-2E-decenamide 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 29761497-9 2018 The indomethacin significantly attenuated the increases of PGE2 , IL-6, and IL-8 expression in cells stimulated with compressive force or mechanical vibration combined with compressive force. Indomethacin 4-16 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 29761497-10 2018 In addition, exogenous PGE2 increased IL-6 and IL-8 mRNA and protein expressions in hPDL cells. Dinoprostone 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 30181697-4 2018 Result demonstrated that IL-8 and IL-11 expression were upregulated in LPA-treated MDA-MB-231 cells. lysophosphatidic acid 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 30181697-7 2018 In the case of PKC activation, it was observed that PKCdelta and PKCmu might regulate LPA-induced expression of IL-11 and IL-8, respectively, by using specific PKC subtype inhibitors. lysophosphatidic acid 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 30181697-9 2018 In conclusion, LPA induced the expression of osteolytic cytokines (IL-8 and IL-11) in breast cancer cells by involving different LPA receptors. lysophosphatidic acid 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 30181697-10 2018 Enhanced expression of IL-8 by LPA may be via ROCK, PKCu, PI3K, and NFkB signaling pathways, while enhanced expression of IL-11 might involve PKCdelta signaling pathway. lysophosphatidic acid 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 30110956-5 2018 Only the combination of lutein with malvidin-3-glucoside showed anti-inflammatory synergy in the suppression of interleukin-8, and the synergy was seen at all three ratios tested. 3-glucoside 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 30016752-2 2018 The aim of the study was to evaluate the influence of PDT with delta-aminolevulinic acid (ALA-PDT) used in sub-lethal dose on the interleukins secretion (IL-6, IL-8 and IL-10) by the residual colon cancer cells (CCC) under hypoxia-like conditions (addition of cobalt chloride- CoCl2). Aminolevulinic Acid 63-88 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 30016752-2 2018 The aim of the study was to evaluate the influence of PDT with delta-aminolevulinic acid (ALA-PDT) used in sub-lethal dose on the interleukins secretion (IL-6, IL-8 and IL-10) by the residual colon cancer cells (CCC) under hypoxia-like conditions (addition of cobalt chloride- CoCl2). Alanine 90-93 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 30016752-6 2018 After ALA-PDT we found no change in the IL-6 level secreted by SW480 cells, but decrease of IL-6, IL-10 secretion by SW620 cells, an increase in the IL-8 secreted by both cells lines. Alanine 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 29901427-8 2018 Ferulic acid significantly ameliorated HUVEC radiation injury, as evidenced by increases in cell viability and angiogenesis and decreases in G2/M cell cycle arrest and levels of high mobility group box 1 protein (HMGB1), interleukin (IL)-6 and IL-8. ferulic acid 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 30157189-9 2018 Pre-treatment with vitamin D decreased CXCL8 and further decreased IL-6 production in PM-stimulated cultures, an effect abrogated by inhibition of G6PD with DHEA, supporting a role for this pathway in the anti-inflammatory actions of vitamin D. Vitamin D 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 39-44 29953960-0 2018 Exosomes derived from calcium oxalate-exposed macrophages enhance IL-8 production from renal cells, neutrophil migration and crystal invasion through extracellular matrix. Calcium Oxalate 22-37 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 30089134-5 2018 Suppression or neutralization of the BZ-induced IL-8 potentiates the BZ cytotoxic and anti-proliferative effect in TNBC cells. Bortezomib 37-39 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 30089134-5 2018 Suppression or neutralization of the BZ-induced IL-8 potentiates the BZ cytotoxic and anti-proliferative effect in TNBC cells. Bortezomib 69-71 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 30123110-0 2018 Role of CXCR1 and Interleukin-8 in Methamphetamine-Induced Neuronal Apoptosis. Methamphetamine 35-50 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 30123110-10 2018 In addition, IL-8 expression and release were increased in METH-exposed U87MG cells, which is regulated by NF-kappaB pathway. Methamphetamine 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 30123110-11 2018 Neuronal apoptosis was attenuated by siCXCR1 after METH treatment in the co-cultured cells, which can be reversed after exposure to recombinant IL-8. Methamphetamine 51-55 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 30123110-13 2018 Highlights -Methamphetamine exposure upregulated the expression of CXCR1.-Methamphetamine exposure increased the expression of interleukin-8 through nuclear factor-kappa B pathway.-Activation of CXCR1 by interleukin-8 induces an increase in methamphetamine-related neuronal apoptosis. Methamphetamine 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 30123110-13 2018 Highlights -Methamphetamine exposure upregulated the expression of CXCR1.-Methamphetamine exposure increased the expression of interleukin-8 through nuclear factor-kappa B pathway.-Activation of CXCR1 by interleukin-8 induces an increase in methamphetamine-related neuronal apoptosis. Methamphetamine 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 204-217 30123110-13 2018 Highlights -Methamphetamine exposure upregulated the expression of CXCR1.-Methamphetamine exposure increased the expression of interleukin-8 through nuclear factor-kappa B pathway.-Activation of CXCR1 by interleukin-8 induces an increase in methamphetamine-related neuronal apoptosis. Methamphetamine 74-89 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 30123110-13 2018 Highlights -Methamphetamine exposure upregulated the expression of CXCR1.-Methamphetamine exposure increased the expression of interleukin-8 through nuclear factor-kappa B pathway.-Activation of CXCR1 by interleukin-8 induces an increase in methamphetamine-related neuronal apoptosis. Methamphetamine 74-89 C-X-C motif chemokine ligand 8 Homo sapiens 204-217 30123110-13 2018 Highlights -Methamphetamine exposure upregulated the expression of CXCR1.-Methamphetamine exposure increased the expression of interleukin-8 through nuclear factor-kappa B pathway.-Activation of CXCR1 by interleukin-8 induces an increase in methamphetamine-related neuronal apoptosis. Methamphetamine 241-256 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 30123110-13 2018 Highlights -Methamphetamine exposure upregulated the expression of CXCR1.-Methamphetamine exposure increased the expression of interleukin-8 through nuclear factor-kappa B pathway.-Activation of CXCR1 by interleukin-8 induces an increase in methamphetamine-related neuronal apoptosis. Methamphetamine 241-256 C-X-C motif chemokine ligand 8 Homo sapiens 204-217 30174784-3 2018 The redox cascade during sepsis is mainly initiated by IL-6 and IL-8 stimulation in newborns and includes multiple noxious processes, as direct cell damage induced by reactive oxygen species, activation of gene expression leading to amplification of inflammation and oxidative stress, and impairment of mitochondrial function. Reactive Oxygen Species 167-190 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 30186283-9 2018 Results: Both primary monocytes and THP-1 cells, a human monocytic cell line, respond strongly to CaOx crystals in a dose-dependent manner producing TNF-alpha, IL-1beta, IL-8, and IL-10 transcripts. caox crystals 98-111 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 30109169-9 2018 IL-8 was increased in sunitinib-resistant Caki-2 and SN12K1 cells and decreased in 786-0 without any significant changes in Caki-1. Sunitinib 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 30021676-8 2018 Remarkably, CIC formation was significantly inhibited by IL-8 knockdown and enhanced upon recombinant IL-8 treatment, which correlated with altered cell-cell adhesion and expression of adhesive molecules such as P-cadherin and gamma-catenin. cic 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 29902421-0 2018 An impedimetric immunosensor for highly sensitive detection of IL-8 in human serum and saliva samples: A new surface modification method by 6-phosphonohexanoic acid for biosensing applications. 6-phosphonohexanoic Acid 140-164 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 29902421-1 2018 In this study, we fabricated a sensitive and label-free impedimetric immunosensor based on 6-phosphonohexanoic acid (PHA) modified ITO electrode for detection of interleukin-8 (IL-8) in human serum and saliva. 6-phosphonohexanoic Acid 91-115 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 29902421-1 2018 In this study, we fabricated a sensitive and label-free impedimetric immunosensor based on 6-phosphonohexanoic acid (PHA) modified ITO electrode for detection of interleukin-8 (IL-8) in human serum and saliva. 6-phosphonohexanoic Acid 91-115 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 29902421-1 2018 In this study, we fabricated a sensitive and label-free impedimetric immunosensor based on 6-phosphonohexanoic acid (PHA) modified ITO electrode for detection of interleukin-8 (IL-8) in human serum and saliva. 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-hexanoylamine 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 29902421-1 2018 In this study, we fabricated a sensitive and label-free impedimetric immunosensor based on 6-phosphonohexanoic acid (PHA) modified ITO electrode for detection of interleukin-8 (IL-8) in human serum and saliva. 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-hexanoylamine 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 30197422-3 2018 2% agarose gel electrophoresis revealed a predominance of IL-8 in the chronic inflammatory palatine tonsil group compared to tonsillar hyperplasia. Sepharose 3-10 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 30208836-5 2018 SO, ED, and GL stimulated production of pro-inflammatory IFN-gamma, IL-1beta, IL-2, IL-6, IL-8, TNF-alpha and anti-inflammatory IL-10. glycylleucine 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 30021676-8 2018 Remarkably, CIC formation was significantly inhibited by IL-8 knockdown and enhanced upon recombinant IL-8 treatment, which correlated with altered cell-cell adhesion and expression of adhesive molecules such as P-cadherin and gamma-catenin. cic 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 29709340-12 2018 Pretreatment and co-incubation of pulp cells by 5z-7oxozeaenol (1 and 2.5 muM) and U0126 (10 and 20 muM) prevented the IL-1beta-induced IL-8 and uPA expression. 5-7-oxo-zeaenol 48-62 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 29701288-16 2018 Within the limit of this study, the results showed that 12 weeks after BAHS implantation the gene expression of some inflammatory cytokines (IL-8 and IL-1beta) is still relatively high compared with the baseline, steady-state, expression. bahs 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 29890415-6 2018 Montelukast has an inhibitory effect on the inflammatory microenvironment of RA by decreasing the secretion of IL-6, IL-8, MMP-3 and MMP-13 in FLSs induced by IL-1beta. montelukast 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 29935159-5 2018 In a glucocorticoid resistance model using human monocytes (THP-1 cell line) differentiated into macrophage-like cells we observed that exposure to 1 mM tertiary butyl hydroperoxide (t-BuOOH) for 4 h significantly hampered the anti-inflammatory action of cortisol assessed as attenuation of the interleukin (IL)-8 production. n-Butylhydroperoxide 162-181 C-X-C motif chemokine ligand 8 Homo sapiens 295-313 29935159-5 2018 In a glucocorticoid resistance model using human monocytes (THP-1 cell line) differentiated into macrophage-like cells we observed that exposure to 1 mM tertiary butyl hydroperoxide (t-BuOOH) for 4 h significantly hampered the anti-inflammatory action of cortisol assessed as attenuation of the interleukin (IL)-8 production. di-tert-butyl peroxide 183-190 C-X-C motif chemokine ligand 8 Homo sapiens 295-313 29396047-0 2018 Fisetin inhibits TNF-alpha/NF-kappaB-induced IL-8 expression by targeting PKCdelta in human airway epithelial cells. fisetin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 30092684-5 2018 Our findings indicate that SBDE-mediated pro-inflammatory effects are predominantly due to the induction of neutrophilic chemokine IL-8. sbde 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 28679068-0 2018 Berberine hydrochloride counteracts enhanced IL-8 expression induced by SN 38 in AGS cells. berberine chloride 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 28679068-0 2018 Berberine hydrochloride counteracts enhanced IL-8 expression induced by SN 38 in AGS cells. Irinotecan 72-77 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 28679068-3 2018 BER could down-regulate the enhanced IL-8 expression through down-regulating ERK1/2 and p38 MAPK over-activation induced by SN 38. Irinotecan 124-129 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 28679068-4 2018 The increased IL-8 mediated adhesive ability of AGS cells to HUVECs induced by SN 38, could be reduced by BER. Irinotecan 79-84 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 29709340-12 2018 Pretreatment and co-incubation of pulp cells by 5z-7oxozeaenol (1 and 2.5 muM) and U0126 (10 and 20 muM) prevented the IL-1beta-induced IL-8 and uPA expression. U 0126 83-88 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 29709340-13 2018 5z-7oxozeaenol and U0126 also attenuated the IL-1beta-induced IL-8 and uPA secretion. 5-7-oxo-zeaenol 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 29709340-13 2018 5z-7oxozeaenol and U0126 also attenuated the IL-1beta-induced IL-8 and uPA secretion. U 0126 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 30018026-4 2018 Mutational analysis of the IL-8 promoter revealed that it was not the AP-1 binding site, but rather the NF-kappaB site that was essential to connect resveratrol stimulation with the transcriptional activation of the IL-8 gene. Resveratrol 149-160 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 29928974-5 2018 We found that the ability to inhibit IL-8 secretion correlated with the amount of proanthocyanidins and was associated to the not edible parts of chestnut in all the tested varieties. Proanthocyanidins 82-99 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 29928974-8 2018 The bioactive components of chestnut fruits inhibit IL-8 secretion by impairing NF-kappaB signaling and by other mechanisms, thus opening new applications of proanthocyanidins for inflammation-based diseases. Proanthocyanidins 158-175 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 29901202-0 2018 CXCL8 and CXCL11 chemokine secretion in dermal fibroblasts is differentially modulated by vanadium pentoxide. vanadium pentoxide 90-108 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 30018026-0 2018 Resveratrol stimulation induces interleukin-8 gene transcription via NF-kappaB. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 30018026-4 2018 Mutational analysis of the IL-8 promoter revealed that it was not the AP-1 binding site, but rather the NF-kappaB site that was essential to connect resveratrol stimulation with the transcriptional activation of the IL-8 gene. Resveratrol 149-160 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 30018026-2 2018 As part of a search for resveratrol-regulated target genes we analyzed the gene encoding the chemokine interleukin-8 (IL-8) which is regulated by AP-1. Resveratrol 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 103-116 30018026-2 2018 As part of a search for resveratrol-regulated target genes we analyzed the gene encoding the chemokine interleukin-8 (IL-8) which is regulated by AP-1. Resveratrol 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 30018026-5 2018 Thus, the NF-kappaB site of the IL-8 gene functions as resveratrol-responsive element. Resveratrol 55-66 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 30018026-3 2018 Here, we show that treatment of HEK293 cells with resveratrol induced the expression of IL-8 and activated transcription of a chromatin-embedded IL-8 promoter-controlled reporter gene. Resveratrol 50-61 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 30018026-3 2018 Here, we show that treatment of HEK293 cells with resveratrol induced the expression of IL-8 and activated transcription of a chromatin-embedded IL-8 promoter-controlled reporter gene. Resveratrol 50-61 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 30018026-7 2018 These data were corroborated by an experiment showing that incubation of the cells with the NF-kappaB inhibitor JSH-23 attenuated resveratrol-induced activation of the IL-8 promoter and reduced the cellular NF-kappaB activity following stimulation of the cells with resveratrol. Resveratrol 130-141 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 30018026-8 2018 The protein kinase extracellular signal-regulated protein kinase ERK1/2 was identified to function as signal transducer connecting resveratrol stimulation with the activation of NF-kappaB and IL-8 promoter-controlled transcription. Resveratrol 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 30018026-9 2018 We conclude that resveratrol, proposed to exhibit anti-inflammatory activity, stimulates expression of the pro-inflammatory chemokine IL-8 via NF-kappaB, which is known as an important mediator of inflammatory processes. Resveratrol 17-28 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 30078983-10 2018 Both CE-CKC emulsions inhibited the secretion of IL-17 (from anti-CD3/anti-CD28-stimulated TCD4), TNFalpha, IFN-gamma, and IL-2 (from anti-CD3-/anti-CD28-stimulated PBMCs), and IL-6 and IL-8 (from LPS-stimulated HCE-2). ce-ckc 5-11 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 29105595-12 2018 The 1,25-(OH)2 induction of cathelicidin and suppression of IL-8 highlights a mechanism by which 1,25-(OH)2 supplementation could enhance the pregnant innate immune defenses. 1,25-(oh)2 97-107 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 32559970-8 2018 Silicon, tin and fluoride ions were recovered together (Na2SiF6 + Na2SnF6 + NaF) by careful evaporation of the aqueous solution after SX of nickel. Silicon 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 32559970-8 2018 Silicon, tin and fluoride ions were recovered together (Na2SiF6 + Na2SnF6 + NaF) by careful evaporation of the aqueous solution after SX of nickel. Fluorides 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 30040868-14 2018 CONCLUSION: CS exposure downregulates the expression levels of EP2 and EP4 receptors and stimulates the production of PGE2 and the proinflammatory cytokine IL-8 and TNF-alpha in polyp tissues of CRS patients. Cesium 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 30078983-12 2018 In addition, tyloxapol, another excipient, showed some anti-inflammatory activity on IL-6 and IL-8 in the LPS-stimulated HCE-2 cells. tyloxapol 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 30026883-10 2018 The antioxidant N-acetyl-L-cysteine significantly inhibited the increases in interleukin-8 induced by solutions with particulate matter, regardless of ozone exposure. Acetylcysteine 16-35 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 30026883-12 2018 Conclusion: Ozone may augment the production of interleukin-8 in response to ambient particulate matter by a mechanism unrelated to reactive oxygen species. Ozone 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 28736254-0 2018 Bisphenol A affects trophoblast invasion by inhibiting CXCL8 expression in decidual stromal cells. bisphenol A 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 55-60 30093956-9 2018 Vincamine also exerted anti-inflammatory activities by decreasing IL-6, IL-8, IL-1beta, TNF-alpha, TGF-beta expression. Vincamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 28736254-4 2018 We found that BPA significantly inhibited CXCL8 expression in DSCs, which hindered trophoblast invasion, and activated the phosphorylation of ERK in DSCs. bisphenol A 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 42-47 28736254-5 2018 U0126, an inhibitor of ERK activation, remarkably rescued trophoblast invasion and the inhibition of CXCL8 expression caused by BPA treatment. U 0126 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 28736254-5 2018 U0126, an inhibitor of ERK activation, remarkably rescued trophoblast invasion and the inhibition of CXCL8 expression caused by BPA treatment. bisphenol A 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 29678503-6 2018 Cytokine levels of IL-8, MIP-1beta, IL-6, IFN-gamma, GM-CSF, TNF, IL-2, IL-4, MCP-1, and IL-10 were decreased significantly with caffeine treatment. Caffeine 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 29980718-9 2018 In addition, EhJAB1 binding blocked EhMIF-induced IL-8 production by human epithelial cells. ehmif 36-41 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 30022950-3 2018 TMA also demonstrated anti-inflammatory properties, via reduction of IL-8 expression, thus making TMA a promising agent for treatment of cystic fibrosis. 4,4',6-trimethylangelicin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 30022950-3 2018 TMA also demonstrated anti-inflammatory properties, via reduction of IL-8 expression, thus making TMA a promising agent for treatment of cystic fibrosis. 4,4',6-trimethylangelicin 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 29473951-7 2018 By contrast, low concentrations of 4-HNE, niacin and 3-OHBA down-regulated the expression of pro-inflammatory cytokines IL-6 and IL-8. 4-hydroxy-2-nonenal 35-40 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 29473951-7 2018 By contrast, low concentrations of 4-HNE, niacin and 3-OHBA down-regulated the expression of pro-inflammatory cytokines IL-6 and IL-8. Niacin 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 29473951-7 2018 By contrast, low concentrations of 4-HNE, niacin and 3-OHBA down-regulated the expression of pro-inflammatory cytokines IL-6 and IL-8. 3-ohba 53-59 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 30002111-1 2018 The aim of this research study was to determine the role of 18F-Sodium fluoride (NaF) PET/CT imaging in the assessment of physiologic molecular calcification in the intra-cranial structures. Sodium Fluoride 64-79 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 30002111-10 2018 NaF uptake significantly correlated with HU in the right choroid plexus (r=0.52, P < 0.0001), left choroid plexus (r=0.57, p<0.0001), and epithalamus (r=0.25, P = 0.03). Hydroxyurea 41-43 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 29980681-4 2018 Blocking ERK activation using a MEK inhibitor (U0126) suppressed NE-induced IL-8 secretion and knockdown of proteinase-activated receptor 2 (PAR2) using siRNAs inhibited both NE-induced ERK activation and subsequent IL-8 release, suggesting that NE-induced IL-8 production is dependent on PAR2-mediated ERK activation. U 0126 47-52 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 29973256-2 2018 Functionalized tricalcium phosphate (fTCP) has been incorporated into sodium fluoride (NaF) varnish to enhance the remineralization process. tricalcium phosphate 15-35 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 29973256-2 2018 Functionalized tricalcium phosphate (fTCP) has been incorporated into sodium fluoride (NaF) varnish to enhance the remineralization process. 4-Fluoro-1-(1-(2-thienyl)cyclohexyl)piperidine 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 29973256-2 2018 Functionalized tricalcium phosphate (fTCP) has been incorporated into sodium fluoride (NaF) varnish to enhance the remineralization process. Sodium Fluoride 70-85 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 29973256-3 2018 NaF varnish with the adjunctive application of silver nitrate (AgNO3) solution is effective in arresting dentine caries. Silver Nitrate 47-61 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 29973256-3 2018 NaF varnish with the adjunctive application of silver nitrate (AgNO3) solution is effective in arresting dentine caries. Silver Nitrate 63-68 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 29973256-12 2018 DISCUSSION: The effectiveness of the topical application of a 25% AgNO3 solution followed by a 5% NaF varnish with fTCP in arresting coronal dentine caries among preschool children remains unknown. 4-Fluoro-1-(1-(2-thienyl)cyclohexyl)piperidine 115-119 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 29512121-10 2018 Paradoxically, ketorolac increased the release of CXCL1 and IL-8 in prostaglandin E2 and chondroitin sulphate-stimulated synovial cells in vitro. Ketorolac 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 29512121-10 2018 Paradoxically, ketorolac increased the release of CXCL1 and IL-8 in prostaglandin E2 and chondroitin sulphate-stimulated synovial cells in vitro. Dinoprostone 68-84 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 29512121-10 2018 Paradoxically, ketorolac increased the release of CXCL1 and IL-8 in prostaglandin E2 and chondroitin sulphate-stimulated synovial cells in vitro. Chondroitin Sulfates 89-109 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 29702023-1 2018 OBJECTIVE: The aim of this article is to present examples in which sodium fluoride labelled with 18F (NaF) bone PET/CT would be a useful adjunct to guide complex clinical decisions about the staging, restaging, and treatment approach for patients with skeletal metastases and benign causes of NaF activity that can be mistaken for bone metastases. Sodium Fluoride 67-82 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 29702023-1 2018 OBJECTIVE: The aim of this article is to present examples in which sodium fluoride labelled with 18F (NaF) bone PET/CT would be a useful adjunct to guide complex clinical decisions about the staging, restaging, and treatment approach for patients with skeletal metastases and benign causes of NaF activity that can be mistaken for bone metastases. Sodium Fluoride 67-82 C-X-C motif chemokine ligand 8 Homo sapiens 293-296 29221667-12 2018 In vitro IL-8 production by IL-27 and IL-37 pre-treated neutrophils and monocytes was significantly inhibited even after heme addition. Heme 121-125 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 29555399-2 2018 Given the similarities in vascular calcification and bone formation, 18F-sodium fluoride (18F-NaF) is now considered a novel marker of vascular calcification. 18f-sodium fluoride 69-88 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 29749433-11 2018 Results from the present study suggested that reparixin and SCH527123 may be promising therapeutic agents for the treatment of pancreatic cancer by inhibiting the IL-8/CXCR1/2 signaling cascade. 2-hydroxy-N,N-dimethyl-3-(2-((1-(5-methylfuran-2-yl)propyl)amino)-3,4-dioxocyclobut-1-enylamino)benzamide 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 30016181-13 2018 As expected, UFH decreased LPS-induced IL-1beta, TNF-alpha, IL-6, IL-8, and IL-18 protein levels, suggesting that UFH has an anti-inflammatory effect on THP-1 cells by interrupting the MAPK, NF-kappaB, and c-Jun signaling pathways. Heparin 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 29630729-0 2018 Rho-kinase inhibitor Y-27632 downregulates LPS-induced IL-6 and IL-8 production via blocking p38 MAPK and NF-kappaB pathways in human gingival fibroblasts. Y 27632 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 29630729-13 2018 CONCLUSIONS: Rho-kinase inhibitor Y-27632 downregulates LPS-induced IL-6 and IL-8 production by blocking NF-kappaB and p38 MAPK activation in HGFs. Y 27632 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 29803436-13 2018 Interestingly, a microbial combination producing high amounts of butyrate was able to reduce IL-8 expression in HT-29 cells co-incubated with TNFalpha. Butyrates 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 29758489-4 2018 Fisetin significantly inhibited COX-2 expression and reduced prostaglandin E2 production, and it suppressed the levels of IL-8, CCL5, monocyte chemotactic protein 1, tumor necrosis factor alpha, and IL-6. fisetin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 29749433-8 2018 Treatment with either reparixin or SCH527123 yielded dose-dependent growth suppressive effects on HPAC, Capan-1 and AsPC-1 cells that may have otherwise undergone robust proliferation upon IL-8 stimulation. reparixin 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 29749433-8 2018 Treatment with either reparixin or SCH527123 yielded dose-dependent growth suppressive effects on HPAC, Capan-1 and AsPC-1 cells that may have otherwise undergone robust proliferation upon IL-8 stimulation. 2-hydroxy-N,N-dimethyl-3-(2-((1-(5-methylfuran-2-yl)propyl)amino)-3,4-dioxocyclobut-1-enylamino)benzamide 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 29749433-9 2018 In addition, reparixin or SCH527123 treatment inhibited CXCR1/2-mediated signal transduction, as demonstrated by the decreased phosphorylation levels of effector molecules STAT3, AKT, ERK and S6 that are downstream of the IL-8/CXCR1/2 signaling cascade in HPAC cells. reparixin 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 29749433-9 2018 In addition, reparixin or SCH527123 treatment inhibited CXCR1/2-mediated signal transduction, as demonstrated by the decreased phosphorylation levels of effector molecules STAT3, AKT, ERK and S6 that are downstream of the IL-8/CXCR1/2 signaling cascade in HPAC cells. 2-hydroxy-N,N-dimethyl-3-(2-((1-(5-methylfuran-2-yl)propyl)amino)-3,4-dioxocyclobut-1-enylamino)benzamide 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 29749433-11 2018 Results from the present study suggested that reparixin and SCH527123 may be promising therapeutic agents for the treatment of pancreatic cancer by inhibiting the IL-8/CXCR1/2 signaling cascade. reparixin 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 30016181-13 2018 As expected, UFH decreased LPS-induced IL-1beta, TNF-alpha, IL-6, IL-8, and IL-18 protein levels, suggesting that UFH has an anti-inflammatory effect on THP-1 cells by interrupting the MAPK, NF-kappaB, and c-Jun signaling pathways. Heparin 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 30938600-2 2018 In previous studies, povidone iodine (PVP-I), a widely used bactericidal antiseptic, and sodium fluoride (NaF), used to foster remineralization of enamel, were applied sequentially topically and shown to be safe and effective. Sodium Fluoride 89-104 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 30938600-3 2018 The study aim was to characterize the kinetics of iodine and fluoride following topical application of a single combination PVP-I and NaF anticaries varnish in healthy adults. Iodine 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 30938600-3 2018 The study aim was to characterize the kinetics of iodine and fluoride following topical application of a single combination PVP-I and NaF anticaries varnish in healthy adults. Fluorides 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 29555399-11 2018 A negative correlation was observed between 18F-NaF uptake and smooth muscle cell staining (IOD: r = -.710, P = .049). Fluorine-18 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 29966605-0 2018 Clioquinol increases the expression of interleukin-8 by down-regulating GATA-2 and GATA-3. Clioquinol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 29704670-5 2018 The results demonstrated that isorhamnetin attenuated LPS-induced release of PGE2, NO, IL-6, and IL-8 in HGFs. 3-methylquercetin 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 29966605-10 2018 Electrophoresis mobility shift assays using a probe corresponding to -159/-113 of the human IL-8 gene revealed two major shifted bands, one of which was increased and the other was decreased by clioquinol. Clioquinol 194-204 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 29966605-5 2018 The global analysis and quantitative PCR demonstrated that the mRNA level of interleukin-8 (IL-8) was significantly increased when SH-SY5Y neuroblastoma cells were treated with clioquinol. Clioquinol 177-187 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 29966605-5 2018 The global analysis and quantitative PCR demonstrated that the mRNA level of interleukin-8 (IL-8) was significantly increased when SH-SY5Y neuroblastoma cells were treated with clioquinol. Clioquinol 177-187 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 29966605-13 2018 Genome editing against GATA-2 or GATA-3, not GATA-4 significantly enhanced clioquinol-induced IL-8 mRNA expression. Clioquinol 75-85 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 29966605-6 2018 An enzyme-linked immunosorbent assay also demonstrated that clioquinol induced the secretion of IL-8 into culture media. Clioquinol 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 29966605-14 2018 On the other hand, the stable expression of GATA-2 or GATA-3 attenuated clioquinol-induced IL-8 mRNA expression and IL-8 secretion. Clioquinol 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 29966605-7 2018 Promoter analyses on SH-SY5Y cells revealed that a region responsive to clioquinol exists between -152 and -144 of the human IL-8 gene, which contains a consensus GATA-binding site sequence. Clioquinol 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 29966605-14 2018 On the other hand, the stable expression of GATA-2 or GATA-3 attenuated clioquinol-induced IL-8 mRNA expression and IL-8 secretion. Clioquinol 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 29966605-15 2018 These results suggest that the clioquinol-induced suppression of GATA-2 and GATA-3 expression mediates the up-regulation of IL-8. Clioquinol 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 29508465-7 2018 Knockdown of Nrf2 attenuated the effect of casticin on production of IL-6 and IL-8, expression of MUC5AC, collagen type I, and fibronectin in 16-HBE cells. casticin 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 29508465-5 2018 The results showed that lipopolysaccharide induced the mRNA and protein levels of IL-6, IL-8, MUC5AC, collagen type I, and fibronectin in 16-HBE cells, whereas casticin treatment significantly inhibited the induction of lipopolysaccharide. casticin 160-168 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 29425105-5 2018 RESULTS: In this study, using R&D Systems ELISA kits, EDTA plasma samples and serum samples with a pre-centrifugation delay longer than 24 h had an IL16 concentration higher than 313 pg/mL, and an IL8 concentration higher than 125 pg/mL, respectively. Edetic Acid 58-62 C-X-C motif chemokine ligand 8 Homo sapiens 201-204 29793168-5 2018 Oxysterols treatment significantly altered differentiated Caco-2 cells redox status, leading to oxidant species production and a decrease of GSH levels, after 1 h exposure, followed by an increase of cytokines production, IL-6 and IL-8, after 24 h. Oxysterol cell treatment also induced after 48 h an increase of NO release, due to the induction of iNOS. Oxysterols 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 231-235 29793168-5 2018 Oxysterols treatment significantly altered differentiated Caco-2 cells redox status, leading to oxidant species production and a decrease of GSH levels, after 1 h exposure, followed by an increase of cytokines production, IL-6 and IL-8, after 24 h. Oxysterol cell treatment also induced after 48 h an increase of NO release, due to the induction of iNOS. Oxysterols 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 231-235 30034287-1 2018 We incidentally identified gallbladder activity on 18F sodium fluoride (NaF) positron emission tomography/computed tomography (PET/CT) bone images in five patients. Sodium Fluoride 55-70 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 29425105-6 2018 EDTA plasma samples with a pre-centrifugation delay longer than 48 h had an IL16 concentration higher than 897 pg/mL, citrate plasma samples had an IL8 concentration higher than 21.5 pg/mL and serum samples had an IL8 concentration higher than 528 pg/mL. Edetic Acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 214-217 29425105-6 2018 EDTA plasma samples with a pre-centrifugation delay longer than 48 h had an IL16 concentration higher than 897 pg/mL, citrate plasma samples had an IL8 concentration higher than 21.5 pg/mL and serum samples had an IL8 concentration higher than 528 pg/mL. Citric Acid 118-125 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 29925859-8 2018 We observed a significant correlation between ERK1/2 phosphorylation and IL-8 expression, suggesting that ERK1/2 modulates the ozone-mediated IL-8 response; however, we found that simultaneous inhibition of both kinases was required to achieve the greatest IL-8 inhibition. Ozone 127-132 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 29940963-6 2018 RESULTS: TBEC and AMs showed stronger pro-inflammatory cytokine (e.g., IL-8) responses to PIC and LPS, respectively. tbec 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 29940963-6 2018 RESULTS: TBEC and AMs showed stronger pro-inflammatory cytokine (e.g., IL-8) responses to PIC and LPS, respectively. Poly I-C 90-93 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 29940963-11 2018 PIC-stimulated TBEC and LPS-stimulated AMs from smokers vs. non-smokers produced more IL-8. Poly I-C 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 29932110-6 2018 Of these, only (2-(1,2-diphenyl-1H-indol-3-yl)ethanamine (DPIE) showed a synergistic increase in inflammatory molecules and cytokine production (IL-6, IL-8, and COX-2) at both mRNA and protein levels in IL-1&beta;-stimulated GFs. 1,2-Diphenyltryptamine 16-56 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 29932110-6 2018 Of these, only (2-(1,2-diphenyl-1H-indol-3-yl)ethanamine (DPIE) showed a synergistic increase in inflammatory molecules and cytokine production (IL-6, IL-8, and COX-2) at both mRNA and protein levels in IL-1&beta;-stimulated GFs. dpie 58-62 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 29925859-7 2018 Recent evidence suggests that the MAP kinases ERK1/2 and p38 mediate ozone-induced IL-8 transcription, thus we hypothesized that differences in their activation may control IL-8 inter-individual variability. Ozone 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 29925859-7 2018 Recent evidence suggests that the MAP kinases ERK1/2 and p38 mediate ozone-induced IL-8 transcription, thus we hypothesized that differences in their activation may control IL-8 inter-individual variability. Ozone 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 29924840-9 2018 In general, the crude leaf extracts amplified the anti-inflammatory response when compared with ketoprofen, particularly reducing the production of IL-8, a mediator involved in neutrophil recruitment during tissue damage. Ketoprofen 96-106 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 29925859-8 2018 We observed a significant correlation between ERK1/2 phosphorylation and IL-8 expression, suggesting that ERK1/2 modulates the ozone-mediated IL-8 response; however, we found that simultaneous inhibition of both kinases was required to achieve the greatest IL-8 inhibition. Ozone 127-132 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 29925859-8 2018 We observed a significant correlation between ERK1/2 phosphorylation and IL-8 expression, suggesting that ERK1/2 modulates the ozone-mediated IL-8 response; however, we found that simultaneous inhibition of both kinases was required to achieve the greatest IL-8 inhibition. Ozone 127-132 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 29865262-6 2018 Simvastatin or fluvastatin caused IL-8 (interleukin-8) suppression, but increased hBD-2 mRNA expression in Salmonella-infected SW480 cells. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 29704506-10 2018 RSV also inhibited inflammation injury of HaCaT cells by reducing productions of IL-6, IL-8, and TNF-alpha. Resveratrol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 29660434-8 2018 BDP/FOR and SB203580 showed the highest inhibitory effect on epithelial IL-8, whereas endothelial ICAM-1 was never affected by BDP/FOR and PDTC. SB 203580 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 29899223-8 2018 In contrast, patients with high pre-interventional IL-6 and IL-8 serum levels not only poorly responded to TACE but had a significantly impaired overall survival. Chlorotrianisene 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 29922598-8 2018 Psoralen and angelicin also markedly decreased the mRNA expression and release of inflammatory cytokines (interleukin [IL]-1beta and IL-8) by THP-1 cells in a dose-dependent manner. Ficusin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 29922598-8 2018 Psoralen and angelicin also markedly decreased the mRNA expression and release of inflammatory cytokines (interleukin [IL]-1beta and IL-8) by THP-1 cells in a dose-dependent manner. angelicin 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 29895782-2 2018 EtOH increased senescence activity, levels of reactive oxygen species (ROS) and the expression of cell cycle regulators (p53, p21 and p16) and senescence-associated secretory phenotype (SASP) genes (interleukin [IL]-1beta, IL-6, IL-8 and tumor necrosis factor-alpha) in HPDLCs and cementoblasts. Ethanol 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 229-265 29865262-6 2018 Simvastatin or fluvastatin caused IL-8 (interleukin-8) suppression, but increased hBD-2 mRNA expression in Salmonella-infected SW480 cells. Fluvastatin 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 29446169-5 2018 RESULTS: Physiological normoxia (5% O2 ) decreased SA-beta-Gal-positive cells and SASP including interleukin-6 (IL-6) and IL-8 compared with cultured cells in 21% O2 . Oxygen 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 29368548-5 2018 We found that the omega-6 PUFA arachidonic acid (AA), but not omega-3 PUFAs or SFAs, upregulates IL-6 and CXCL8 release. omega-6 pufa 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 106-111 29693201-0 2018 IL-8 regulates the doxorubicin resistance of colorectal cancer cells via modulation of multidrug resistance 1 (MDR1). Doxorubicin 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 29368548-5 2018 We found that the omega-6 PUFA arachidonic acid (AA), but not omega-3 PUFAs or SFAs, upregulates IL-6 and CXCL8 release. Arachidonic Acid 31-47 C-X-C motif chemokine ligand 8 Homo sapiens 106-111 29334172-1 2018 We have previously reported that silica nanoparticles (SiNPs) of nominal size 50 nm (Si50) induce the pro-inflammatory cytokines CXCL8 and IL-6 in BEAS-2B cells, via mechanisms involving MAPK p38, TACE-mediated TGF-alpha release and the NF-kappaB pathway. Silicon Dioxide 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 129-134 29693201-3 2018 Cytokine expression analysis revealed that IL-8, while not FGF-2, EGF, TGF-beta, IL-6, or IL-10, was significantly increased in Dox-resistant CRC cells as compared with their corresponding parental cells. Doxorubicin 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 29693201-4 2018 Targeted inhibition of IL-8 via siRNAs or its inhibitor reparixin can increase the Dox sensitivity of HCT-116/Dox and SW480/Dox cells. Doxorubicin 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 29693201-4 2018 Targeted inhibition of IL-8 via siRNAs or its inhibitor reparixin can increase the Dox sensitivity of HCT-116/Dox and SW480/Dox cells. Doxorubicin 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 29693201-4 2018 Targeted inhibition of IL-8 via siRNAs or its inhibitor reparixin can increase the Dox sensitivity of HCT-116/Dox and SW480/Dox cells. Doxorubicin 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 29693201-5 2018 The si-IL-8 can decrease the mRNA and protein expression of multidrug resistance 1 (MDR1, encoded by ABCB1), while has no effect on the expression of multidrug resistance-associated protein 1 (ABCC1), in CRC Dox-resistant cells. Doxorubicin 208-211 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 29693201-7 2018 BAY 11-7082, the inhibitor of NF-kappaB, suppressed the recombination IL-8 (rIL-8) induced upregulation of ABCB1. 3-(4-methylphenylsulfonyl)-2-propenenitrile 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 29693201-10 2018 These results suggested that IL-8 regulates the Dox resistance of CRC cells via modulation of MDR1 through IKK-beta/p65 signals. Doxorubicin 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 29693201-11 2018 The targeted inhibition of IL-8 might be an important potential approach to overcome the clinical Dox resistance in CRC patients. Doxorubicin 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 29581231-0 2018 Intestinal mucin activates human dendritic cells and IL-8 production in a glycan-specific manner. Polysaccharides 74-80 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 29604316-4 2018 Where present, F was 1150 ppm as NaF; Zn was 0.3% as ZnCl2. Fluorine 15-16 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 29404796-9 2018 Plasma IL-6 and IL-8 levels after surgery were significantly lower in the PMMA group than in the PS group, while other cytokines measured in this study were not significantly different. Polymethyl Methacrylate 74-78 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 29404796-11 2018 The continuous use of PMMA-CRRT throughout the perioperative period suppressed serum IL-6 and IL-8 concentrations, although there were no differences in clinical outcomes. Polymethyl Methacrylate 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 29431349-3 2018 The aim of our study was to evaluate the effect of active vitamin D3 (VD) on the expression of pro-inflammatory and anti-inflammatory cytokines (IL-6, IL-8, IL-10 and IL-12) in human gingival fibroblasts (hGF) and human periodontal ligament cells (hPDLc) triggered by Porphyromonas gingivalis and Streptococcus pyogenes. Cholecalciferol 58-68 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 30069319-14 2018 In 16HBE airway cells, H2O2 increased IL-6 and IL-8 secretion in conjunction with ERK1/2 and NF-kappaB activation. Hydrogen Peroxide 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 29704403-6 2018 In differentiated Caco-2 cell monolayers as a model of the small intestinal epithelium, complexation of gliadin with GTE reduces gliadin-stimulated monolayer permeability and the release of interleukin (IL)-6 and IL-8. gte 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 29658573-7 2018 The results indicated that A549 had increased levels of IL-6, IL-8 and TNF-alpha when cultured with nicotine when compared with the control cells. Nicotine 100-108 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 29027074-0 2018 Uptake of Radium-223 Dichloride and Early [18F]NaF PET Response Are Driven by Baseline [18F]NaF Parameters: a Pilot Study in Castration-Resistant Prostate Cancer Patients. radium Ra 223 dichloride 10-31 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 29027074-1 2018 PURPOSE: The purpose of this study is to identify predictive factors on baseline [18F]NaF positron emission tomography (PET)/computed tomography (CT) of early response to radium-223 dichloride after 3 cycles of treatment in metastatic castration-resistant prostate cancer patients. 223 dichloride 178-192 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 29027074-14 2018 CONCLUSIONS: SUVmax and SUVmean on baseline [18F]NaF PET/CT are independent predictors of bone lesions" response to 3 cycles of radium-223 dichloride, supporting the use of NaF to select patients more likely to respond to treatment. radium Ra 223 dichloride 128-149 C-X-C motif chemokine ligand 8 Homo sapiens 173-176 29805673-0 2018 Anesthetic drug propofol inhibits the expression of interleukin-6, interleukin-8 and cyclooxygenase-2, a potential mechanism for propofol in suppressing tumor development and metastasis. Propofol 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 29805673-2 2018 The present study demonstrated that propofol may suppress the proliferation of MCF-7 cells and inhibit the expression of interleukin (IL)-6 and IL-8. Propofol 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 29805673-0 2018 Anesthetic drug propofol inhibits the expression of interleukin-6, interleukin-8 and cyclooxygenase-2, a potential mechanism for propofol in suppressing tumor development and metastasis. Propofol 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 29805673-4 2018 Therefore, the mechanism of propofol in suppressing tumor development and metastasis may be associated with the inhibition of IL-6, IL-8 and COX-2. Propofol 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 29672044-0 2018 Andrographolide Antagonizes TNF-alpha-Induced IL-8 via Inhibition of NADPH Oxidase/ROS/NF-kappaB and Src/MAPKs/AP-1 Axis in Human Colorectal Cancer HCT116 Cells. andrographolide 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 29656143-2 2018 DESIGN: Both knees of 15 participants with unilateral reconstructed ACL tears and unaffected contralateral knees were scanned using a simultaneous 3.0T PET-MRI system following injection of 18F-sodium fluoride (18F-NaF). 18f-sodium fluoride 190-209 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 29573703-4 2018 The aim of this work was to study the extent of the protective effect of the antioxidant N-acetylcysteine (NAC) over the proinflammatory state (IL-6 and IL-8), oxidative stress (reactive oxygen species, ROS), and CFTR levels, caused by Cigarette Smoke Extract (CSE) in Calu-3 airway epithelial cells. Acetylcysteine 89-105 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 29573703-4 2018 The aim of this work was to study the extent of the protective effect of the antioxidant N-acetylcysteine (NAC) over the proinflammatory state (IL-6 and IL-8), oxidative stress (reactive oxygen species, ROS), and CFTR levels, caused by Cigarette Smoke Extract (CSE) in Calu-3 airway epithelial cells. Acetylcysteine 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 29802207-5 2018 We report that human basophils are refractory to Treg-mediated suppression and found that Tregs stimulate resting basophils to induce the expression of activation markers including CD69, CD203c, and CD13 and the release of basophil cytokines including IL-13, IL-8, and IL-4. tregs 90-95 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 29510260-7 2018 CONCLUSIONS: ALA-PDT in sublethal doses might influence colon cancer cell"s progression and invasion by reducing the secretion of IL-6, IL-10 and increasing the IL-8 concentration with higher values in the more malignant cell line. Alanine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 29477863-7 2018 These divergences in ROS production seem to be correlated with the different extension of intracellular signaling pathways activation and, by consequence, with distinct transcription kinetics of genes such as HMOX1, IL8, IL1B and CD86. Reactive Oxygen Species 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 216-219 29501468-10 2018 Moderate direct correlations were observed between vitamin D and IL-8, IL-10, and IFN-gamma in the prospective group of 16 brain-dead patients (IL-8: r = 0.5, p = 0.049; IL-10 r = 0.67, p = 0.005; IFN-gamma r = 0.6, p = 0.015). Vitamin D 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 29501468-10 2018 Moderate direct correlations were observed between vitamin D and IL-8, IL-10, and IFN-gamma in the prospective group of 16 brain-dead patients (IL-8: r = 0.5, p = 0.049; IL-10 r = 0.67, p = 0.005; IFN-gamma r = 0.6, p = 0.015). Vitamin D 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 29501468-13 2018 In brain-dead patients, vitamin D serum levels correlated with plasma IL-8, IL-10 and IFN-gamma. Vitamin D 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 29672044-4 2018 However, the effect and molecular mechanisms of IL-8 expression by andrographolide remain obscure in human colorectal cancer cells. andrographolide 67-82 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 29672044-5 2018 The present study was aimed to investigate the effects of andrographolide on TNF-alpha-induced IL-8 expression and its underlying mechanisms. andrographolide 58-73 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 29875665-10 2018 The GLPG and/or SHB treatments restored the inhibitory effects of acetate on IL-6 and IL-8 production and the inhibitory effects of butyrate or propionate on IL-6 production, but not on IL-8. Acetates 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 29672044-6 2018 We found that andrographolide concentration-dependently inhibited TNF-alpha-induced IL-8 mRNA (2.23 +- 0.15 fold at 20 muM) and protein expression (4.78 +- 0.31 fold at 20 muM) and reduced the IL-8 transcriptional activity (2.59 +- 0.25 fold at 20 muM). andrographolide 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 29672044-6 2018 We found that andrographolide concentration-dependently inhibited TNF-alpha-induced IL-8 mRNA (2.23 +- 0.15 fold at 20 muM) and protein expression (4.78 +- 0.31 fold at 20 muM) and reduced the IL-8 transcriptional activity (2.59 +- 0.25 fold at 20 muM). andrographolide 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 29672044-12 2018 Taken together, andrographolide antagonizes TNF-alpha-induced IL-8 via inhibition of NADPH oxidase/ROS/NF-kappaB and Src/MAPKs/AP-1 signaling pathways in HCT116 colorectal cancer cells and then suppresses angiogenesis in the tumor microenvironment. andrographolide 16-31 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 29672044-12 2018 Taken together, andrographolide antagonizes TNF-alpha-induced IL-8 via inhibition of NADPH oxidase/ROS/NF-kappaB and Src/MAPKs/AP-1 signaling pathways in HCT116 colorectal cancer cells and then suppresses angiogenesis in the tumor microenvironment. Reactive Oxygen Species 99-102 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 29882863-1 2018 This work provides a cost-effective approach for preparing functional polymeric fibers used for removing uranium (U(VI)) from carbonate solution containing NaF. Uranium 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 29875665-12 2018 TSA showed similar effects on IL-8 production and VCAM-1 expression as butyrate and propionate. trichostatin A 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 29882863-1 2018 This work provides a cost-effective approach for preparing functional polymeric fibers used for removing uranium (U(VI)) from carbonate solution containing NaF. Carbonates 126-135 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 29875665-14 2018 Conclusion: Activation of GPR41/43 mediates the effects of acetate on IL-6 and IL-8 production and the effects of butyrate and propionate on IL-6 production. Acetates 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 29875665-15 2018 Furthermore, inhibition of HDACs mediates the effects of butyrate and propionate on IL-8 production, VCAM-1 expression, and PBMC adhesion to an endothelial monolayer. Butyrates 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 32254344-7 2018 In human whole blood, CS@OVA-13 and CS@OVA-65 were phagocytosed with a significantly higher ratio by granulocytes and monocytes, leading to the higher secretion of TNF-alpha, IL-1beta and IL-8, and a larger extent of platelet activation than CS@HSA-10 and CS@HSA-57, respectively. Chitosan 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 32254344-7 2018 In human whole blood, CS@OVA-13 and CS@OVA-65 were phagocytosed with a significantly higher ratio by granulocytes and monocytes, leading to the higher secretion of TNF-alpha, IL-1beta and IL-8, and a larger extent of platelet activation than CS@HSA-10 and CS@HSA-57, respectively. Chitosan 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 32254344-7 2018 In human whole blood, CS@OVA-13 and CS@OVA-65 were phagocytosed with a significantly higher ratio by granulocytes and monocytes, leading to the higher secretion of TNF-alpha, IL-1beta and IL-8, and a larger extent of platelet activation than CS@HSA-10 and CS@HSA-57, respectively. Chitosan 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 32254344-7 2018 In human whole blood, CS@OVA-13 and CS@OVA-65 were phagocytosed with a significantly higher ratio by granulocytes and monocytes, leading to the higher secretion of TNF-alpha, IL-1beta and IL-8, and a larger extent of platelet activation than CS@HSA-10 and CS@HSA-57, respectively. Chitosan 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 29683320-4 2018 KCO-4 inhibited the oversecretion of inflammatory mediators (i.e., NO, TNF-alpha, IL-1beta, IL-8, iNOS, and COX-2). kco-4 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 29793566-3 2018 Test group lesions were treated using resin infiltration followed by five percent topical sodium fluoride (NaF) application versus five percent NaF alone in the control group. Sodium Fluoride 90-105 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 29785126-11 2018 Suppression of TGF-beta signaling by OT-101 led to upregulation of IL-8, IL-15, IP-10, and HGF. ot-101 37-43 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 29785126-13 2018 The mixed analysis of covariance model that examined the levels of 19 cyto-/chemokines with OS as the covariate at each of the time points resulted in IL-8 and IL-15 exhibiting a significant association with OS during Cycle 1 of therapy. Osmium 92-94 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 29785126-14 2018 In the whole-blood culture model, the cytokines with the most pronounced increase after OT-101 treatment were IL-1beta, IL-8, and MCP-1. ot-101 88-94 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 29785126-16 2018 Levels of IL-8 and IL-15 during Cycle 1 were positively associated with OS across 12 patients with PAC and served as potential biomarkers for treatment outcome following OT-101 therapy. ot-101 170-176 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 29634256-2 2018 Mild hydrothermal reactions with uranyl acetate as a precursor yielded 1, 7, and the monoclinic polymorph of NaU2F9, whereas direct reactions between UF4 and NaF led to the formation of 2 and orthorhombic NaU2F9 (3). uf4 150-153 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 29634256-2 2018 Mild hydrothermal reactions with uranyl acetate as a precursor yielded 1, 7, and the monoclinic polymorph of NaU2F9, whereas direct reactions between UF4 and NaF led to the formation of 2 and orthorhombic NaU2F9 (3). nau2f9 205-211 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 29439091-8 2018 In vitro, CXL induced significant release of Gal-1 in keratocyte supernatants (116+-18 ng/mL, P<0.05) and decreased inflammatory biomarkers as interleukin (IL)-6, IL-8, matrix metalloproteinase (MMP)-2 and MMP-9. Cyclohexanols 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 29648435-5 2018 The FEC-NaFSI constructs the mechanically strong and ion-permeable interlayer containing NaF and ionic compounds such as Na2CO3 and sodium alkylcarbonates. sodium carbonate 121-127 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 29648435-5 2018 The FEC-NaFSI constructs the mechanically strong and ion-permeable interlayer containing NaF and ionic compounds such as Na2CO3 and sodium alkylcarbonates. sodium alkylcarbonates 132-154 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 29471239-5 2018 NaF increased expression of miR-200c-3p and miR-200c-3p inhibitor reduced activation of SaoS2 induced by NaF via targeting Noggin to repress BMP4/Smad. saos2 88-93 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 29471239-5 2018 NaF increased expression of miR-200c-3p and miR-200c-3p inhibitor reduced activation of SaoS2 induced by NaF via targeting Noggin to repress BMP4/Smad. saos2 88-93 C-X-C motif chemokine ligand 8 Homo sapiens 105-108 30052195-7 2018 Taurine and aloe extract significantly (p < 0.05) reduced IL-lalpha and IL-8 production in vitro and in vivo after topical application of formulations containing AlCl3. Taurine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 61-79 29143360-10 2018 In addition, FPTHQ treatment increased the protein levels of MMP3 and the mRNA levels of IL-6 and IL-8 in A2780 cells, indicating the appearance of senescence-associated secretary phenotype (SASP) in the cells. fpthq 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 29410518-10 2018 Furthermore, rifaximin reduced IL-8 secretion from pregnane X receptor-expressing T84 colonic epithelial cells. Rifaximin 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 30398154-4 2018 LPS-treated HUVECs cultured in low magnesium showed up-regulation of mRNA expression for pro-inflammatory factors and the expression of cytokine proteins, including IL-2, IL-3, IL-8, IL-15 and MCP-1. Magnesium 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 29568907-0 2018 Differential modulation by vanadium pentoxide of the secretion of CXCL8 and CXCL11 chemokines in thyroid cells. vanadium pentoxide 27-45 C-X-C motif chemokine ligand 8 Homo sapiens 66-71 29575797-6 2018 RESULT: NTHi induced production of large amounts of IL-1beta, IL-6, and IL-8 in adult-control BAL cells, however BAL cells from PBB airways appeared refractory to NTHi stimulation. nthi 8-12 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 29908644-12 2018 Concomitantly, LY294002 inhibited CdCl2-induced IL-8 in JEG-3 cells. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 29908644-12 2018 Concomitantly, LY294002 inhibited CdCl2-induced IL-8 in JEG-3 cells. Cadmium Chloride 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 29300263-8 2018 The level of proinflammatory cytokine IL-8 was elevated in BAK-treated cells. Benzalkonium Compounds 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 30006643-10 2018 Body mass index positively correlated with 18F-FDG uptake in the soft tissue (r=0.53, P<0.0001), osseous compartment (r=0.58, P<0.0001) and 18F-NaF uptake in the joint (r=0.37, P=0.0001). Fluorodeoxyglucose F18 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 29243408-6 2018 RESULTS: Micronucleated cells (P < .00) and MN (P < .00) were higher in individuals exposed to chlorhexidine (CHX), followed by chlorine dioxide (ClO2 ), potassium nitrate (KNO3 ), and sodium fluoride (NaF), amine fluoride (AmF), and normal saline. Chlorhexidine 101-114 C-X-C motif chemokine ligand 8 Homo sapiens 208-211 29243408-6 2018 RESULTS: Micronucleated cells (P < .00) and MN (P < .00) were higher in individuals exposed to chlorhexidine (CHX), followed by chlorine dioxide (ClO2 ), potassium nitrate (KNO3 ), and sodium fluoride (NaF), amine fluoride (AmF), and normal saline. Chlorhexidine 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 208-211 29550716-5 2018 The NaF treatment associated with CSE recovered the bond strength values of SD/CSE and associated with CSE demonstrated lower microTBS than other groups, although significantly higher than DD (p < 0.05). microtbs 126-134 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 29616124-4 2018 Incubation with sodium citrate for 24 h revealed that the levels of interleukin-1beta (IL-1beta), IL-8 and tumor necrosis factor increased with an increasing of dose of sodium citrate, whereas the IL-6 levels exhibited only a slight alteration. Sodium Citrate 16-30 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 29616124-4 2018 Incubation with sodium citrate for 24 h revealed that the levels of interleukin-1beta (IL-1beta), IL-8 and tumor necrosis factor increased with an increasing of dose of sodium citrate, whereas the IL-6 levels exhibited only a slight alteration. Sodium Citrate 169-183 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 29908644-6 2018 RESULTS: TNF-alpha, IL-8 and IL-6 mRNAs were elevated in CdCl2-treated JEG-3 cells. Cadmium Chloride 57-62 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 29908644-8 2018 Moreover, keratinocyte chemokine (KC), a functional analogue of human IL-8, was increased in maternal serum and amniotic fluid from CdCl2-exposed mice. Cadmium Chloride 132-137 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 29413962-5 2018 Moreover, we demonstrated that the expression of NF-kappaB, COX-2, IL-8, and MMP-13 were elevated subsequent to inhibition of SIRT1/AMPK/PGC-1alpha/PPAR-gamma pathway by homocysteine, thereby causing detrimental effects on chondrocytes. Homocysteine 170-182 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 29413957-7 2018 2-ClHA and its alkyne analogue interfered with protein palmitoylation, induced ER-stress markers, reduced the ER ATP content, and activated transcription and secretion of interleukin (IL)-6 as well as IL-8. 2-chlorohexadecanoic acid 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 29413957-7 2018 2-ClHA and its alkyne analogue interfered with protein palmitoylation, induced ER-stress markers, reduced the ER ATP content, and activated transcription and secretion of interleukin (IL)-6 as well as IL-8. Alkynes 15-21 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 30052195-7 2018 Taurine and aloe extract significantly (p < 0.05) reduced IL-lalpha and IL-8 production in vitro and in vivo after topical application of formulations containing AlCl3. Aluminum Chloride 165-170 C-X-C motif chemokine ligand 8 Homo sapiens 61-79 29570290-3 2018 The addition of NaF as a mineralizer increases the crystallinity of gamma-zirconium phosphate, which forms micrometer-sized uniformly shaped rectangular platelets. gamma-zirconium phosphate 68-93 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 29854096-0 2018 Cafestol Inhibits Cyclic-Strain-Induced Interleukin-8, Intercellular Adhesion Molecule-1, and Monocyte Chemoattractant Protein-1 Production in Vascular Endothelial Cells. cafestol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 29854096-9 2018 The addition of zinc protoporphyrin IX, sirtinol, or Sirt1 silencing (transfected with Sirt1 siRNA) significantly attenuated cafestol-mediated modulatory effects on cyclic-strain-stimulated ICAM-1, MCP-1, and IL-8 secretion. cafestol 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 29755453-7 2018 The binding of a CLEC10A-specific bivalent ligand (the MUC-1 peptide glycosylated with N-acetylgalactosamine) is limited to CD1c+ DCs and enhances the cytokine secretion (namely TNFalpha, IL-8, and IL-10) induced by TLR 7/8 stimulation. Acetylgalactosamine 87-108 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 29922277-9 2018 Interleukin (IL)-6 and IL-8 mRNA and protein were induced in both cell types after treatment with AMC particles, whereas exposure to CoCr particles resulted in significantly upregulated IL-6 and IL-8 protein contents in PBMCs only. 7-amino-4-methylcoumarin 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 29922277-9 2018 Interleukin (IL)-6 and IL-8 mRNA and protein were induced in both cell types after treatment with AMC particles, whereas exposure to CoCr particles resulted in significantly upregulated IL-6 and IL-8 protein contents in PBMCs only. 7-amino-4-methylcoumarin 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 29850636-2 2018 Our objective was to analyze any association between the oxygen levels at blood sampling and plasma levels of the interleukins IL-6, IL-1beta, IL-10, and IL-8 and TNF-alpha in preterm newborns under mechanical ventilation (MV) in their first two days. Oxygen 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 29850636-11 2018 In the high oxygen group, IL-6, IL-8, and TNF-alpha plasma levels increased significantly after two hours under MV. Oxygen 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 29713062-9 2018 siRNA downregulation of 2-deoxy-D-ribose 5-phosphate (DR5P) aldolase, which is needed for DR5P to enter glycolysis, also suppressed the induction of NADPH and IL-8 in TP-expressing cells. dr5p 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 29731195-8 2018 Cellular ROS production was increased by PM treatment, and antioxidant N-acetyl cysteine pretreatment prevented induction of inflammatory cytokines IL-8 and MMP-1. Acetylcysteine 71-88 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 29702553-13 2018 Hydroxyethyl starch 70 kDa significantly increased the recovery of interleukin (IL)-8 in human serum in vitro when compared with Ringer&rsquo;s lactate. Hydroxyethyl starch 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 67-85 29507072-4 2018 IL-8 levels were negatively correlated with the number of ceftriaxone doses administered (r = -0.315; P = 0.031). Ceftriaxone 58-69 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 29713468-13 2018 However, we observed that the mRNA expression of IL-8 in placenta was reduced by maternal resveratrol. Resveratrol 90-101 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 29626212-7 2018 Co-treatment of high glucose with palmitic acid potentiated the expression of several DR-relevant angiogenic and inflammatory targets, including PTGS2 (COX-2) and CXCL8 (IL-8). Glucose 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 163-168 29518371-4 2018 The aim of this study was to elucidate the underlying mechanism of NTAPP-induced IL-8 expression in human keratinocyte HaCaT cells. Plasma Gases 67-72 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 29518371-8 2018 High intracellular K+ concentrations suppressed NTAPP-induced IL-8 mRNA expression, and the K+ ionophore valinomycin (Val) enhanced the induction of IL-8 mRNA. Plasma Gases 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 29518371-8 2018 High intracellular K+ concentrations suppressed NTAPP-induced IL-8 mRNA expression, and the K+ ionophore valinomycin (Val) enhanced the induction of IL-8 mRNA. Valinomycin 105-116 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 29518371-8 2018 High intracellular K+ concentrations suppressed NTAPP-induced IL-8 mRNA expression, and the K+ ionophore valinomycin (Val) enhanced the induction of IL-8 mRNA. Valinomycin 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 29518371-9 2018 Moreover, NTAPP stimulated activation of ERK MAP kinase and the ERK inhibitor prevented NTAPP-induced IL-8 mRNA expression. Plasma Gases 10-15 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 29518371-9 2018 Moreover, NTAPP stimulated activation of ERK MAP kinase and the ERK inhibitor prevented NTAPP-induced IL-8 mRNA expression. Plasma Gases 88-93 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 29268188-10 2018 Semi-quantitative detection of IL-8 consumption in HUVEC cells in low oxygen condition was also achieved. Oxygen 70-76 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 29626212-7 2018 Co-treatment of high glucose with palmitic acid potentiated the expression of several DR-relevant angiogenic and inflammatory targets, including PTGS2 (COX-2) and CXCL8 (IL-8). Glucose 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 29626212-7 2018 Co-treatment of high glucose with palmitic acid potentiated the expression of several DR-relevant angiogenic and inflammatory targets, including PTGS2 (COX-2) and CXCL8 (IL-8). Palmitic Acid 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 163-168 29626212-7 2018 Co-treatment of high glucose with palmitic acid potentiated the expression of several DR-relevant angiogenic and inflammatory targets, including PTGS2 (COX-2) and CXCL8 (IL-8). Palmitic Acid 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 29293370-0 2018 Initial experience with 18F-sodium fluoride (NaF) PET-CT: a viable functional biomarker in symptomatic Os acromiale. 18f-sodium fluoride 24-43 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 29293370-4 2018 18F Sodium Fluoride (NaF) Positron Emission Tomography -CT (PET-CT) is an emerging and highly sensitive modality for oncological skeletal staging, and can show a variety of non-malignant uptake. Sodium Fluoride 4-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 29293370-5 2018 We have analysed the relationship between 18F-NaF uptake in OA and associated symptoms of shoulder pain. Fluorine-18 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 29452068-5 2018 Here, we found that glycyrrhizin (20 or 40 muM) inhibited histamine-induced the mRNA expression and secretion of mucin 5 subtype AC (MUC5AC), interleukin (IL)-6 and IL-8 in HNEpCs. Histamine 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 29176750-3 2018 High levels of C-X-C motif chemokine ligand 8/interleukin-8 (CXCL8/IL-8), the most potent chemokine to attract neutrophils to sites of infection, are detected in the sputum of both patient groups and might cause the high neutrophil influx in the airways. c-x-c 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 61-66 29176750-3 2018 High levels of C-X-C motif chemokine ligand 8/interleukin-8 (CXCL8/IL-8), the most potent chemokine to attract neutrophils to sites of infection, are detected in the sputum of both patient groups and might cause the high neutrophil influx in the airways. c-x-c 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 29452068-5 2018 Here, we found that glycyrrhizin (20 or 40 muM) inhibited histamine-induced the mRNA expression and secretion of mucin 5 subtype AC (MUC5AC), interleukin (IL)-6 and IL-8 in HNEpCs. Glycyrrhizic Acid 20-32 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 29875577-9 2018 The presence of glycerol-supplemented L. reuteri significantly reduced the expression of IL-8 and hBD-2 on HaCat cells (P < 0.05). Glycerol 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 29405435-8 2018 Increased IL-8 levels, measured within 24 hours, were associated with PGD3, more ECMO use, higher donor paO2 , younger donor age, but not with other short-or long-term outcome. pao2 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 29223613-1 2018 AIM: To investigate the usefulness of a quantitative parameter (maximum standardised uptake value [SUVmax]) of 18F-sodium fluoride (NaF) positron-emission tomography (PET)/computed tomography (CT) for the evaluation of temporomandibular joint (TMJ) disorder (TMD). 18f-sodium fluoride 111-130 C-X-C motif chemokine ligand 8 Homo sapiens 132-135 29875577-10 2018 Conclusion: Glycerol-supplemented L. reuteri reduced the expression of IL-8 and hBD-2, and the results may be proof of principle for a probiotic approach to combating inflammation. Glycerol 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 29256007-5 2018 RESULTS: IL-1beta decreased genomic methylation of human intestinal epithelial cells and induced demethylation at cg-specific sites at the promoter of pro-inflammatory genes IL6 and IL8; conversely it did not change the methylation of the IL10 promoter. cysteinylglycine 114-116 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 29643687-3 2018 18F-sodium fluoride positron emission tomography-computed tomography (18F-NaF PET-CT) demonstrates increased radiotracer uptake at body of D4 vertebra. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 29230506-5 2018 The effect of iPA on IL-8 and RANTES secretion was determined by ELISA, and the activation and expression of signaling molecules and selenoproteins were studied by Western blot. Isopentenyladenosine 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 29230506-7 2018 RESULTS: We demonstrated for the first time that iPA prevents IL-8 and RANTES release in TNFalpha-stimulated CF cells and this effect is mediated by increasing the expression of the direct NFkappaB inhibitor IkappaBalpha and decreasing the levels of STAT3. Isopentenyladenosine 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 29127842-8 2018 Dynamic compliance was significantly improved in the budesonide group on days 3 (p=0.018) and 5 (p=0.011) The levels of CXCL-8 and IL-6 diminished on days 3-5 after start of budesonide (p<0.05). Budesonide 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 120-126 29127842-9 2018 CONCLUSION: In COPD patients on MV, nebulized budesonide was associated with reduced BAL CXCL8 and IL-6 levels and neutrophil numbers as well as an improvement in ventilatory mechanics and facilitated weaning. Budesonide 46-56 C-X-C motif chemokine ligand 8 Homo sapiens 89-94 29353318-9 2018 CONCLUSIONS: VEGF and IL-8 production in the pleural cavity appear to accelerate the progression of PPE to empyema, by enhancing vascular permeability associated with inflammation. ppe 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 29380034-6 2018 In the absence of an airway insult, we expected to find no evidence of airway inflammation; however, transcripts for several asthma-associated cytokines, including IL17A, IL1A, and IL8, were elevated in the tracheas of bethanechol-treated piglets. Bethanechol 219-230 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 29614734-3 2018 A preliminary bioactive study shows that (+)-liphagal is a selective kinase (PI3K alpha) inhibitor, while (+)-frondosin B is shown to inhibit the binding of the cytokine interleukin-8 (IL-8) to its receptor, CX-CLR1/2. liphagal 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 170-183 29351123-1 2018 OBJECTIVE: Determination of the accuracy of sodium fluorine-18-fluoride (F-NaF) PET/computed tomography (CT) for the evaluation of bone metastases, and the impact on patient management in breast cancer patients. sodium fluorine-18-fluoride 44-71 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 29166379-6 2018 In stimulated Caco-2 cells, vernix-MAG was more effective than vernix-FFA in suppressing IL-8 and NF-kappaB. vernix-mag 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 29166379-6 2018 In stimulated Caco-2 cells, vernix-MAG was more effective than vernix-FFA in suppressing IL-8 and NF-kappaB. vernix-ffa 63-73 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 29408666-5 2018 Acute exposure to high MPA or ROQ C concentrations induced an increase of IL-8 secretion. roquefortine 30-35 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 29337216-0 2018 In vitro lung epithelial cell transport and anti-interleukin-8 releasing activity of liposomal ciprofloxacin. Ciprofloxacin 95-108 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 29337216-5 2018 The inhibitory activities of Lipo-CPFX and CPFX against lipopolysaccharide (LPS)-induced IL-8 release were assessed in a co-incubation or pre-incubation mode. lipo-cpfx 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 29337216-5 2018 The inhibitory activities of Lipo-CPFX and CPFX against lipopolysaccharide (LPS)-induced IL-8 release were assessed in a co-incubation or pre-incubation mode. Ciprofloxacin 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 29337216-8 2018 Lipo-CPFX was equipotent to CPFX in the anti-IL-8 releasing activity upon 24 h co-incubation with LPS. lipo-cpfx 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 29337216-8 2018 Lipo-CPFX was equipotent to CPFX in the anti-IL-8 releasing activity upon 24 h co-incubation with LPS. Ciprofloxacin 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 29337216-9 2018 Additionally, Lipo-CPFX, but not CPFX, retained the anti-IL-8 releasing activity even 24 h after pre-incubation. lipo-cpfx 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 29436743-3 2018 Plasma eCBs and NAE profiles were correlated with self-rated oral cavity pain intensities, depressive symptomatology and plasma IL-8 levels. ecbs 7-11 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 29436743-3 2018 Plasma eCBs and NAE profiles were correlated with self-rated oral cavity pain intensities, depressive symptomatology and plasma IL-8 levels. N-acylethanolamines 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 29614734-3 2018 A preliminary bioactive study shows that (+)-liphagal is a selective kinase (PI3K alpha) inhibitor, while (+)-frondosin B is shown to inhibit the binding of the cytokine interleukin-8 (IL-8) to its receptor, CX-CLR1/2. frondosin B 106-121 C-X-C motif chemokine ligand 8 Homo sapiens 170-183 29337216-9 2018 Additionally, Lipo-CPFX, but not CPFX, retained the anti-IL-8 releasing activity even 24 h after pre-incubation. Ciprofloxacin 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 29337216-10 2018 In conclusion, Lipo-CPFX enabled slower absorptive lung epithelial cell transport and uptake of ciprofloxacin, apparently via the lipid bilayer fusion mechanism, and the sustained inhibitory activity against LPS-induced IL-8 release, compared to CPFX. lipo-cpfx 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 220-224 29614734-3 2018 A preliminary bioactive study shows that (+)-liphagal is a selective kinase (PI3K alpha) inhibitor, while (+)-frondosin B is shown to inhibit the binding of the cytokine interleukin-8 (IL-8) to its receptor, CX-CLR1/2. frondosin B 106-121 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 29337216-10 2018 In conclusion, Lipo-CPFX enabled slower absorptive lung epithelial cell transport and uptake of ciprofloxacin, apparently via the lipid bilayer fusion mechanism, and the sustained inhibitory activity against LPS-induced IL-8 release, compared to CPFX. Ciprofloxacin 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 220-224 29596311-6 2018 However, interleukin-8 was different between pre- and post-tests (p < 0.001) in both groups (&Delta; = 7.61 and 5.61 pg/mL) as were cholesterol levels (p < 0.05), with no interaction between groups. Adenosine Monophosphate 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 29615908-7 2018 Acetate, butyrate and propionate reduced IL-6 and IL-8 levels and the magnitude was dependent on the incubation times. Acetates 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 29615908-7 2018 Acetate, butyrate and propionate reduced IL-6 and IL-8 levels and the magnitude was dependent on the incubation times. Butyrates 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 29615908-7 2018 Acetate, butyrate and propionate reduced IL-6 and IL-8 levels and the magnitude was dependent on the incubation times. Propionates 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 29615908-12 2018 Conclusion: SCFA, including acetate, butyrate and propionate, influenced LPS- or TNFalpha-induced endothelial activation by inhibiting the production of IL-6 and IL-8, and reducing the expression of VCAM-1 and subsequent cell adhesion. Acetates 28-35 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 29615908-12 2018 Conclusion: SCFA, including acetate, butyrate and propionate, influenced LPS- or TNFalpha-induced endothelial activation by inhibiting the production of IL-6 and IL-8, and reducing the expression of VCAM-1 and subsequent cell adhesion. Propionates 50-60 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 29965469-6 2018 To effectively regenerate TiO2, the removal efficiency of Si polymers on TiO2 via sodium fluoride (NaF) was studied. Silicon 58-60 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 29713361-4 2018 AGNE reduced histamine secretion, production of proinflammatory cytokines including interleukin- (IL-) 1beta, IL-4, IL-6, IL-8, and IL-10, and expression of cyclooxygenase- (COX-) 2 in HMC-1 cells. agne 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 29306057-7 2018 In addition, compared with the placebo, omega-3 and vitamin E co-supplementation down-regulated interleukin-8 (IL-8) (P = 0.003) and tumor necrosis factor alpha (TNF-alpha) expression (P = 0.001) in PBMC of PCOS women. Fatty Acids, Omega-3 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 29306057-7 2018 In addition, compared with the placebo, omega-3 and vitamin E co-supplementation down-regulated interleukin-8 (IL-8) (P = 0.003) and tumor necrosis factor alpha (TNF-alpha) expression (P = 0.001) in PBMC of PCOS women. Fatty Acids, Omega-3 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 29306057-7 2018 In addition, compared with the placebo, omega-3 and vitamin E co-supplementation down-regulated interleukin-8 (IL-8) (P = 0.003) and tumor necrosis factor alpha (TNF-alpha) expression (P = 0.001) in PBMC of PCOS women. Vitamin E 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 29306057-7 2018 In addition, compared with the placebo, omega-3 and vitamin E co-supplementation down-regulated interleukin-8 (IL-8) (P = 0.003) and tumor necrosis factor alpha (TNF-alpha) expression (P = 0.001) in PBMC of PCOS women. Vitamin E 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 29306057-9 2018 CONCLUSION: Omega-3 and vitamin E co-supplementation was effective in improving parameters of mental health, and gene expression of PPAR-gamma, IL-8 and TNF-alpha of women with PCOS. Fatty Acids, Omega-3 12-19 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 29306057-9 2018 CONCLUSION: Omega-3 and vitamin E co-supplementation was effective in improving parameters of mental health, and gene expression of PPAR-gamma, IL-8 and TNF-alpha of women with PCOS. Vitamin E 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 29965469-6 2018 To effectively regenerate TiO2, the removal efficiency of Si polymers on TiO2 via sodium fluoride (NaF) was studied. titanium dioxide 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 29965469-6 2018 To effectively regenerate TiO2, the removal efficiency of Si polymers on TiO2 via sodium fluoride (NaF) was studied. Sodium Fluoride 82-97 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 29965469-7 2018 The results showed that NaF could remove Si monomer and polymer from TiO2, and the regenerated TiO2 could be reused with a stable adsorption performance. Silicon 41-43 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 29515108-4 2018 Our studies reveal that sunitinib triggers two resistance-promoting signaling pathways in RCC cells, which emanate from the endoplasmic reticulum (ER) stress response: a PERK-driven ER stress response that induces expression of the pro-tumorigenic cytokines IL-6, IL-8, and TNF-alpha, and a TRAF2-mediated NF-kappaB survival program that protects tumor cells against cell death. Sunitinib 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 29965469-7 2018 The results showed that NaF could remove Si monomer and polymer from TiO2, and the regenerated TiO2 could be reused with a stable adsorption performance. titanium dioxide 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 29515108-5 2018 PERK blockade completely prevents sunitinib-induced expression of IL-6, IL-8 and TNF-alpha, whereas NF-kappaB inhibition reinstates sensitivity of RCC cells to sunitinib both in vitro and in vivo. Sunitinib 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 29965469-7 2018 The results showed that NaF could remove Si monomer and polymer from TiO2, and the regenerated TiO2 could be reused with a stable adsorption performance. titanium dioxide 95-99 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 29965469-8 2018 In situ ATR-FTIR spectroscopy suggested that NaF desorbed the Si monomer and polymer effectively. Silicon 62-64 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 29965469-9 2018 When spent TiO2 was regenerated with NaOH and NaF in three treatment cycles, As and Si desorption rates were 86.8%-100.3% and 67.9%-82.0%, respectively. titanium dioxide 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 29331857-7 2018 Baicalin alleviated IL-1beta-induced inflammatory injury, as it increased cell viability, decreased cell apoptosis and repressed the production of IL-6, IL-8 and TNF-alpha. baicalin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 29513760-6 2018 Several inflammatory molecules upregulated by tumor necrosis factor-alpha in human retinal vascular endothelial cells were markedly reduced by metformin, including nuclear factor kappa B p65 (NFkappaB p65), intercellular adhesion molecule-1 (ICAM-1), monocyte chemotactic protein-1 (MCP-1), and interleukin-8 (IL-8). Metformin 143-152 C-X-C motif chemokine ligand 8 Homo sapiens 295-308 29513760-6 2018 Several inflammatory molecules upregulated by tumor necrosis factor-alpha in human retinal vascular endothelial cells were markedly reduced by metformin, including nuclear factor kappa B p65 (NFkappaB p65), intercellular adhesion molecule-1 (ICAM-1), monocyte chemotactic protein-1 (MCP-1), and interleukin-8 (IL-8). Metformin 143-152 C-X-C motif chemokine ligand 8 Homo sapiens 310-314 29692858-10 2018 Dieckol and eckol attenuated the expression of inflammatory cytokines such as tumor necrosis factor- (TNF-) alpha, interleukin- (IL-) 1beta, IL-6, and IL-8 in human epidermal keratinocytes stimulated with PM10. dieckol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 29155016-3 2018 In this report, we demonstrated that in vitro, DZ2002 significantly decreased the expression of pro-inflammatory cytokines and adhesion molecule including IL-1alpha, IL-1beta, IL-6, IL-8, TNF-alpha and ICAM-1 by inhibiting the phosphorylation of p38 MAPK, ERK and JNK in TNF-alpha/IFN-gamma-stimulated HaCaT human keratinocytes. methyl 4-(adenin-9-yl)-2-hydroxybutanoate 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 29412148-6 2018 A specific inhibitor of p38MAPK, SB203580 significantly decreased the secretion of IL-6 and IL-8, the major components of SASPs. SB 203580 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 29412148-7 2018 Additionally, treatment of senescent astrocytes with NF-kappaB inhibitor, BAY 11-7092, also suppressed the secretion of IL-6 and IL-8, suggesting NF-kappaB was required for SASP. bay 11-7092 74-85 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 29520786-9 2018 IL-8 and monocyte chemotactic protein-1 mRNA expression could be suppressed by the vitamin D pathway. Vitamin D 83-92 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 29450421-3 2018 The decomposition of FEC provides a NaF-containing solid electrolyte interphase with homogenous morphology and high modulus, leading to stable sodium deposition and high Coulombic efficiency (88% over 50 cycles) of the sodium metal anode. Sodium 143-149 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 29450421-3 2018 The decomposition of FEC provides a NaF-containing solid electrolyte interphase with homogenous morphology and high modulus, leading to stable sodium deposition and high Coulombic efficiency (88% over 50 cycles) of the sodium metal anode. Sodium 219-231 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 29284672-1 2018 We have previously reported that PET using 18F-fluoride (NaF PET) for assessment of osseous metastatic disease was associated with substantial changes in intended management in Medicare beneficiaries participating in the National Oncologic PET Registry (NOPR). Fluoride ion f-18 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 29531654-9 2018 Results: Plasma TNF-alpha, IL-8, and ET-1 were significantly elevated in the BPC group than in the steady state group and the controls. bpc 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 29486738-10 2018 IL-6, IL-8 and XIAP showed increased expressions in PTX-treated cells and this over-production effect was inhibited in TLR4-transient knockdown cells. Paclitaxel 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 29427404-6 2018 For some experiments, human neutrophils were incubated with Reparixin (IL-8/CXCL8 receptor blocker) and then analysed as in the in vitro experiments mentioned above. reparixin 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 29427404-6 2018 For some experiments, human neutrophils were incubated with Reparixin (IL-8/CXCL8 receptor blocker) and then analysed as in the in vitro experiments mentioned above. reparixin 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 76-81 29427404-10 2018 Reparixin inhibited human neutrophil activation by both pig and human IL-8 in a dose-dependent fashion. reparixin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 29427404-11 2018 At 0.1 mg/mL, Reparixin inhibited the adhesion of IL-8-activated human neutrophils to pAECs by 84 +- 2.5%. reparixin 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 29644004-6 2018 Glioblastoma stem cells (GSCs) of the mesenchymal (MES) subtype showed dramatically higher expression of IL8 when compared to proneural (PN) GSCs. 2-(N-morpholino)ethanesulfonic acid 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 105-108 29644004-7 2018 Secreted IL-8 derived from MES GSCs induced endothelial proliferation and tube formation, and the MES GBMs had increased counts of proliferating endothelial cells. 2-(N-morpholino)ethanesulfonic acid 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 29644004-7 2018 Secreted IL-8 derived from MES GSCs induced endothelial proliferation and tube formation, and the MES GBMs had increased counts of proliferating endothelial cells. 2-(N-morpholino)ethanesulfonic acid 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 29644004-8 2018 Our results highlight a critical pro-angiogenic role of IL-8 in MES GBMs. 2-(N-morpholino)ethanesulfonic acid 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 29486738-13 2018 CpdA could significantly decrease expressions of IL-6, XIAP and IL-8, as well as excreted IL-8 levels together with reduced cancer viability after PTX treatment. CPDA 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 29486738-13 2018 CpdA could significantly decrease expressions of IL-6, XIAP and IL-8, as well as excreted IL-8 levels together with reduced cancer viability after PTX treatment. CPDA 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 29486738-14 2018 CONCLUSIONS: The acquired TLR4-mediated PTX resistance in BCA and melanoma is explained partly by the paracrine effect of IL-6 and IL-8 released into the tumor microenvironment and over-production of anti-apoptotic protein, XIAP, in BCA cells and importantly CpdA could reduce this effect and sensitize PTX-induced apoptosis in a synergistic manner. Paclitaxel 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 29441606-5 2018 The results showed the mRNA and protein levels of iNOS, VEGF and IL-2, IL-8 and TNF-alpha were significantly increased in PCa and BPH+HP groups compared with BPH group (p < .05), while the AR was significantly lower than those in PCa and BPH+HP groups (p < .05). Hematoporphyrins 134-136 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 29407945-3 2018 Among these derivatives, 4,5-dihydropyridazinone representatives possess promising activity, selectivity towards PDE4 isoenzymes and are able to reduce IL-8 production by human primary polymorphonuclear cells. 4,5-dihydropyridazinone 25-48 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 29355601-0 2018 Nickel ions bind to HSP90beta and enhance HIF-1alpha-mediated IL-8 expression. Nickel 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 29355601-4 2018 In the present study, we compared the effects of Ni2+ and Co2+ on the expression of interleukin (IL)-8 in human monocyte THP-1 cells. Nickel(2+) 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 84-102 29355601-4 2018 In the present study, we compared the effects of Ni2+ and Co2+ on the expression of interleukin (IL)-8 in human monocyte THP-1 cells. Cobalt(2+) 58-62 C-X-C motif chemokine ligand 8 Homo sapiens 84-102 29355601-5 2018 We report that NiCl2 but not CoCl2 induced the expression of IL-8; in contrast, CoCl2 elicited a higher expression of hypoxia-inducible factor-1alpha (HIF-1alpha). nickel chloride 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 29355601-6 2018 The NiCl2-induced expression of IL-8 in late phase was blocked by a HIF-1alpha inhibitor, PX-478, indicating that NiCl2 targets additional factors responsible for activating HIF-1alpha. nickel chloride 4-9 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 29355601-6 2018 The NiCl2-induced expression of IL-8 in late phase was blocked by a HIF-1alpha inhibitor, PX-478, indicating that NiCl2 targets additional factors responsible for activating HIF-1alpha. 2-amino-3-(4'-N,N-bis(2-chloroethyl)amino)phenylpropionic acid N-oxide 90-96 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 29355601-11 2018 These results suggest that HSP90beta plays important roles in Ni2+-induced production of IL-8 and could be a potential target for the regulation of Ni2+-induced inflammation. Nickel(2+) 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 29355601-11 2018 These results suggest that HSP90beta plays important roles in Ni2+-induced production of IL-8 and could be a potential target for the regulation of Ni2+-induced inflammation. Nickel(2+) 148-152 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 29670468-8 2018 Results: SAA-stimulated levels of released IL-6, IL-8, and sVCAM-1 from HCAEC were significantly attenuated by methotrexate, fluvastatin, and etoricoxib. Methotrexate 111-123 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 29444128-7 2018 Regardless of the type of keratinocyte stimulation used, reduction of cytokine IL-8, IL-20 and CCL2 production (both at RNA and protein level) following genistein treatment was visible. Genistein 153-162 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 29670468-8 2018 Results: SAA-stimulated levels of released IL-6, IL-8, and sVCAM-1 from HCAEC were significantly attenuated by methotrexate, fluvastatin, and etoricoxib. Fluvastatin 125-136 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 29670468-8 2018 Results: SAA-stimulated levels of released IL-6, IL-8, and sVCAM-1 from HCAEC were significantly attenuated by methotrexate, fluvastatin, and etoricoxib. Etoricoxib 142-152 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 29670468-12 2018 Methotrexate showed strong beneficial effects for lowering released Il-6, IL-8, and sVCAM-1. Methotrexate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 29393918-6 2018 Pro-inflammatory cytokine expression, including IL-1beta, IL-8, and IL-10, is known to be modulated by TGR5, and was dependent on NP composition, with LCA-modified cores downregulating inflammation. Lithocholic Acid 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 29440746-6 2018 Furthermore, ZnCl2 inhibited Ni2+-induced IL-8 production, correlating with the inhibition of Ni2+ uptake. zinc chloride 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 29440746-6 2018 Furthermore, ZnCl2 inhibited Ni2+-induced IL-8 production, correlating with the inhibition of Ni2+ uptake. Nickel(2+) 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 29440746-6 2018 Furthermore, ZnCl2 inhibited Ni2+-induced IL-8 production, correlating with the inhibition of Ni2+ uptake. Nickel(2+) 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 29440746-7 2018 These results suggested that Ni2+ uptake occurred through Zn2+, Mn2+, and Co2+-sensitive transporters and that the inhibition of Ni2+ uptake resulted in the inhibition of IL-8 production. Nickel(2+) 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 29205563-4 2018 Exceptionally, by addition of 1 % NaF to a suspension of the foldamer in H2 O/THF (95:5), the fluorescence quenching efficiency by TNT vapor significantly increased from about 20 % to more than 90 %. Water 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 29205563-4 2018 Exceptionally, by addition of 1 % NaF to a suspension of the foldamer in H2 O/THF (95:5), the fluorescence quenching efficiency by TNT vapor significantly increased from about 20 % to more than 90 %. tetrahydrofuran 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 29440746-4 2018 In the present study, we investigated the effects of various divalent cations on Ni2+ uptake and Ni2+-induced interleukin (IL)-8 production in the human monocytic cell line, THP-1. Nickel(2+) 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 110-128 29406857-1 2018 BACKGROUND: Fluorine-18-sodium fluoride (18F-NaF) uptake is a marker of active vascular calcification associated with high-risk atherosclerotic plaque. fluorine-18-sodium fluoride 12-39 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 29246853-0 2018 Cafestol, a coffee diterpene, inhibits urotensin II-induced interleukin-8 expression in human umbilical vein endothelial cells. cafestol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 29246853-0 2018 Cafestol, a coffee diterpene, inhibits urotensin II-induced interleukin-8 expression in human umbilical vein endothelial cells. Diterpenes 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 29246853-8 2018 Moreover, cafestol inhibited expression of urotensin II-induced interleukin-8. cafestol 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 64-77 29246853-9 2018 Cafestol"s inhibitory effects on interleukin-8 expression and cellular proliferation induced by urotensin II were significantly abrogated by heme oxygenase-1 silencing, suggesting it may be involved in mediating the effects of cafestol. cafestol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 29246853-10 2018 This study reports that cafestol inhibits urotensin II-induced interleukin-8 expression and cell proliferation via Nrf2/heme oxygenase-1-dependent mechanism in endothelial cells. cafestol 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 29402921-4 2018 Piglets fed the lysine-restricted diet exhibited overexpression of interleukin-8 (IL-8) in the kidney (P < 0.05) and IL-6 and IL-4 in the spleen (P < 0.05). Lysine 16-22 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 29402921-4 2018 Piglets fed the lysine-restricted diet exhibited overexpression of interleukin-8 (IL-8) in the kidney (P < 0.05) and IL-6 and IL-4 in the spleen (P < 0.05). Lysine 16-22 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 29100748-2 2018 This study aimed to explore the roles of endoplasmic reticulum (ER) stress and autophagy in sodium fluoride (NaF)-induced neurotoxicity, focusing on the regulating role of ER stress in autophagy. Sodium Fluoride 92-107 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 29245047-0 2018 Polyriboinosinic-polyribocytidylic acid facilitates interleukin-6, and interleukin-8 secretion in human dermal fibroblasts via the JAK/STAT3 and p38 MAPK signal transduction pathways. Poly I-C 0-39 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 29245047-3 2018 Here, we found that polyI:C enhances IL-6 and IL-8 mRNA expression and induces of IL-6 and IL-8 production in a concentration-dependent and time-dependent manner in HDFs. Poly I-C 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 29245047-3 2018 Here, we found that polyI:C enhances IL-6 and IL-8 mRNA expression and induces of IL-6 and IL-8 production in a concentration-dependent and time-dependent manner in HDFs. Poly I-C 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 29245047-5 2018 Moreover, pretreatment with AG490, a Janus kinase (JAK) inhibitor, inhibited polyI:C-induced STAT3 phosphorylation and subsequent IL-6 and IL-8 release. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 28-33 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 29245047-5 2018 Moreover, pretreatment with AG490, a Janus kinase (JAK) inhibitor, inhibited polyI:C-induced STAT3 phosphorylation and subsequent IL-6 and IL-8 release. Poly I-C 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 29366441-7 2018 Furthermore, hypoxia-induced inflammation by HMGB1 translocation into the cytoplasm results in the release of IL-8 through a ROS-dependent mechanism in upper airway epithelium. ros 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 29245047-6 2018 Conversely, pretreatment with SB203580, a selective inhibitor of p38 MAPK, blocked p38 MAPK phosphorylation and IL-6 and IL-8 expression. SB 203580 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 29245047-7 2018 In conclusion, polyI:C induces IL-6 and IL-8 production in HDFs via the JAK/STAT3 and p38 MAPK signaling pathways. Poly I-C 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 29100748-6 2018 Notably, inhibition of autophagy in NaF-treated SH-SY5Y cells with Wortmannin or Chloroquine decreased, while induction of autophagy by Rapamycin increased the cell viability. Wortmannin 67-77 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 29100748-6 2018 Notably, inhibition of autophagy in NaF-treated SH-SY5Y cells with Wortmannin or Chloroquine decreased, while induction of autophagy by Rapamycin increased the cell viability. Chloroquine 81-92 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 29100748-6 2018 Notably, inhibition of autophagy in NaF-treated SH-SY5Y cells with Wortmannin or Chloroquine decreased, while induction of autophagy by Rapamycin increased the cell viability. Sirolimus 136-145 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 29100748-8 2018 Importantly, mitigation of ER stress by 4-phenylbutyrate in NaF-treated SH-SY5Y cells inhibited the expressions of autophagy markers, and decreased cell apoptosis. 4-phenylbutyric acid 40-56 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 31938199-6 2018 Co-immunoprecipitation (co-IP) was used for identifying interaction of CXCL1 and CXCL8 with CXCR2 in GC cells. 12-(4'-azido-2'-nitrophenoxy)dodecanoyl-coenzyme A 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 81-86 29331734-4 2018 AgNP alone induced dose-related IL-8 production in all models, with higher response observed in THP-1 cells, possibly connected to different protein corona formation in bovine versus human serum. agnp 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 29331734-5 2018 AgNP potentiated LPS-induced IL-8 and TNF-alpha, but not LPS-induced IL-10. agnp 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 29434821-6 2018 Preconditioning with physiological 5% CS for 30, 60 and 120 min was demonstrated to significantly attenuate the release of pathologically mechanical stretch-induced early pro-inflammatory cytokines (TNF-alpha, IL-1beta and IL-8) in alveolar epithelial cells (P<0.05) and significantly reduce the expression of NF-kappaB (P<0.05). Cesium 38-40 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 29434821-8 2018 In the second set of experiments, it was demonstrated that mechanical stretch-induced release of TNF-alpha, IL-1beta and IL-8 was significantly inhibited by both PDTC pretreatment and 5% CS pretreatment alone (all P<0.05). Cesium 187-189 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 29236553-5 2018 lipopolysaccharide co-treatment with progesterone significantly decreased the bacterial endotoxin-induced IL-1beta, TNF-alpha, IL-6, IL-8, and MIP-1alpha secretion. Progesterone 37-49 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 29191392-7 2018 RESULTS: We observed that CAP significantly induces the expression of Artemin, EGF, EG-VEGF (PK1), Endothelin-1 (ET-1), FGF-2 (FGF basic), IL-8 (CXCL8) and uPA in keratinocytes and Angiogenin (ANG), Endostatin (Col18A1), MCP-1 (CCL2), MMP-9, TIMP-1, uPA and VEGF in fibroblasts. cap 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 29415357-3 2018 A urinary IL-8 level of less than 61.25 pg/mL was more sensitive for prediction of CR in IMN patients. Chromium 83-85 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 28600879-10 2018 After N-acetyl cysteine treatment ROS level was partly abolished providing additional enhancement of IL-6 and suppression of IL-8 and VEGF production. Acetylcysteine 6-23 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 28600879-10 2018 After N-acetyl cysteine treatment ROS level was partly abolished providing additional enhancement of IL-6 and suppression of IL-8 and VEGF production. ros 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 29191392-7 2018 RESULTS: We observed that CAP significantly induces the expression of Artemin, EGF, EG-VEGF (PK1), Endothelin-1 (ET-1), FGF-2 (FGF basic), IL-8 (CXCL8) and uPA in keratinocytes and Angiogenin (ANG), Endostatin (Col18A1), MCP-1 (CCL2), MMP-9, TIMP-1, uPA and VEGF in fibroblasts. cap 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 145-150 29207110-0 2018 Acetylshikonin suppresses invasion of Porphyromonas gingivalis-infected YD10B oral cancer cells by modulating the interleukin-8/matrix metalloproteinase axis. acetylshikonin 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 114-127 28801702-7 2018 Then we curiously studied whether the aging MRC-5 cell-conditioned medium could induce EMT in premalignant HaCaT cells, and the results showed that paeonol significantly reduced the clonogenic, migratory, and invasive capacities of premalignant HaCaT cells potentially induced by IL-6 and IL-8. paeonol 148-155 C-X-C motif chemokine ligand 8 Homo sapiens 289-293 29388547-11 2018 Ruxolitinib caused a significant increase in the production of IL-6, IL-8 and TNF-alpha in stimulated cells. ruxolitinib 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 28941582-4 2018 Topical application of the strong contact sensitizer 2,4-dinitrochlorobenzene (DNCB) induced IL-6 and IL-8 secretion in RHS with LC-like cells, whereas no change was observed in reference models. Dinitrochlorobenzene 53-77 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 28941582-4 2018 Topical application of the strong contact sensitizer 2,4-dinitrochlorobenzene (DNCB) induced IL-6 and IL-8 secretion in RHS with LC-like cells, whereas no change was observed in reference models. Dinitrochlorobenzene 79-83 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 28947239-5 2018 In the ALI setup, all three aldehydes caused increased secretion of IL-8, acrolein and crotonaldehyde also increased the gene expression of inflammatory and oxidative stress markers. Aldehydes 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 29113965-8 2018 The increased mitochondrial reactive oxygen species levels of atherosclerotic-MSCs promoted a phenotypic switch characterized by enhanced glycolysis and an altered cytokine secretion (interleukin-6 P<0.0001, interleukin-8/C-X-C motif chemokine ligand 8 P=0.04, and monocyte chemoattractant protein-1/chemokine ligand 2 P=0.01). Reactive Oxygen Species 28-51 C-X-C motif chemokine ligand 8 Homo sapiens 225-255 29441020-4 2018 The elevated levels of IL-6, CRP, IL-8, and TNF-alpha were effectively reduced by EDT treatment. eriodictyol 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 29374001-1 2018 BACKGROUND: Titanium tetrafluoride (TiF4) has regained interest due to new formulations that have been shown to be more effective against tooth demineralization than sodium fluoride (NaF) formulations in vitro and in situ. Sodium Fluoride 166-181 C-X-C motif chemokine ligand 8 Homo sapiens 183-186 29373608-8 2018 Moreover, IL-33-induced IL-8 mRNA and secretion were also suppressed by SP600125. pyrazolanthrone 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 29497482-12 2017 In MCF-7 cells, interleukin-8, angiogenin and vascular endothelial growth factor secretion was significantly increased by high fractional oxygen. Oxygen 138-144 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 29350745-0 2018 TiO2 nanoparticles can selectively bind CXCL8 impacting on neutrophil chemotaxis. titanium dioxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 40-45 29113965-9 2018 Furthermore, treatment of atherosclerotic-MSCs with the reactive oxygen species scavenger N-acetyl-l-cysteine reduced the levels of interleukin-6, interleukin-8/C-X-C motif chemokine ligand 8, and monocyte chemoattractant protein-1/chemokine ligand 2 in the MSC secretome and improved MSCs immunosuppressive capacity (P=0.03). Reactive Oxygen Species 56-79 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 29350745-3 2018 TiO2 NPs were shown to bind to CXCL8 in vitro, causing perturbation of quantification of CXCL8 by ELISA, in both simple and complex protein panels, in a dose-dependent manner. titanium dioxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 31-36 29350745-3 2018 TiO2 NPs were shown to bind to CXCL8 in vitro, causing perturbation of quantification of CXCL8 by ELISA, in both simple and complex protein panels, in a dose-dependent manner. titanium dioxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 89-94 29350745-4 2018 Binding between TiO2 NPs and CXCL8 was demonstrated by protein gel electrophoresis. titanium dioxide 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 29-34 29113965-9 2018 Furthermore, treatment of atherosclerotic-MSCs with the reactive oxygen species scavenger N-acetyl-l-cysteine reduced the levels of interleukin-6, interleukin-8/C-X-C motif chemokine ligand 8, and monocyte chemoattractant protein-1/chemokine ligand 2 in the MSC secretome and improved MSCs immunosuppressive capacity (P=0.03). Reactive Oxygen Species 56-79 C-X-C motif chemokine ligand 8 Homo sapiens 161-191 29350745-5 2018 TiO2 NPs were also shown to inactivate the chemoattractant property of CXCL8 in a dose-dependent manner, suggesting that the binding between TiO2 NPs and CXCL8 is likely to be clinically relevant. titanium dioxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 29350745-5 2018 TiO2 NPs were also shown to inactivate the chemoattractant property of CXCL8 in a dose-dependent manner, suggesting that the binding between TiO2 NPs and CXCL8 is likely to be clinically relevant. titanium dioxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 154-159 29113965-9 2018 Furthermore, treatment of atherosclerotic-MSCs with the reactive oxygen species scavenger N-acetyl-l-cysteine reduced the levels of interleukin-6, interleukin-8/C-X-C motif chemokine ligand 8, and monocyte chemoattractant protein-1/chemokine ligand 2 in the MSC secretome and improved MSCs immunosuppressive capacity (P=0.03). Acetylcysteine 90-109 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 29350745-5 2018 TiO2 NPs were also shown to inactivate the chemoattractant property of CXCL8 in a dose-dependent manner, suggesting that the binding between TiO2 NPs and CXCL8 is likely to be clinically relevant. titanium dioxide 141-145 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 29350745-5 2018 TiO2 NPs were also shown to inactivate the chemoattractant property of CXCL8 in a dose-dependent manner, suggesting that the binding between TiO2 NPs and CXCL8 is likely to be clinically relevant. titanium dioxide 141-145 C-X-C motif chemokine ligand 8 Homo sapiens 154-159 29350745-6 2018 The results of this study disputed the applicability of detection of CXCL8 by ELISA in systems where TiO2 NPs were present. titanium dioxide 101-105 C-X-C motif chemokine ligand 8 Homo sapiens 69-74 29113965-9 2018 Furthermore, treatment of atherosclerotic-MSCs with the reactive oxygen species scavenger N-acetyl-l-cysteine reduced the levels of interleukin-6, interleukin-8/C-X-C motif chemokine ligand 8, and monocyte chemoattractant protein-1/chemokine ligand 2 in the MSC secretome and improved MSCs immunosuppressive capacity (P=0.03). Acetylcysteine 90-109 C-X-C motif chemokine ligand 8 Homo sapiens 161-191 29350745-7 2018 Clinically, the disruption of chemotaxis of neutrophils in response to CXCL8 in the presence of TiO2 might mean a hampered immune response to inflammation in tissues containing TiO2 NPs. titanium dioxide 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 29895165-6 2018 In addition, at a concentration of 25 and 50 mumol/l Kaempferol could significantly reduce the expression of inflammatory mediators such as tumor necrosis factor alpha (TNF-alpha), interleukin-8 (IL-8) and macrophage inflammatory protein 1 alpha (MIP-1alpha) in human promonocytic U937 cells-derived macrophages (dU937) in response to lipopolysaccharides (LPS) stimulation. kaempferol 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 181-194 29350745-7 2018 Clinically, the disruption of chemotaxis of neutrophils in response to CXCL8 in the presence of TiO2 might mean a hampered immune response to inflammation in tissues containing TiO2 NPs. titanium dioxide 177-181 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 29269075-6 2018 Monocytes treated with Docetaxel also displayed an elevated secretion of IL-8 and IL-1beta, but did not promote generation of monocytic myeloid-derived suppressor cells. Docetaxel 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 29321495-5 2018 Moreover, treatment with STS (10 mug/ml) reduced CS extract (CSE)-induced IL-6 and IL-8 secretion in human bronchial epithelial (16HBE) cells. Cesium 49-51 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 29068113-2 2018 Experiments with NaF, NaCl, NaBr, and NaI salts indicate that the Raman shifts of the Au-X- SERS bands correlate with the bond strength of the corresponding covalent interaction. au-x- 86-91 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 29068113-2 2018 Experiments with NaF, NaCl, NaBr, and NaI salts indicate that the Raman shifts of the Au-X- SERS bands correlate with the bond strength of the corresponding covalent interaction. sers 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 28962868-9 2018 HaCaT cells pretreated/treated with FITOPROT also showed normal expression of TNF-R1 and NF-kappaB inflammatory proteins and decreased levels of pro-inflammatory cytokines (TNF, IL-1beta, IL-6 and IL-8). fitoprot 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 29321495-5 2018 Moreover, treatment with STS (10 mug/ml) reduced CS extract (CSE)-induced IL-6 and IL-8 secretion in human bronchial epithelial (16HBE) cells. tanshinone II A sodium sulfonate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 29478513-2 2018 Although glycolysis inhibitors such as sodium fluoride (NaF) in combination with potassium oxalate (KOx) are currently used for overcoming this drawback, their efficacy for stabilizing blood glucose is seemingly limited, and probably lower than that of newer additives such as the citrate buffer. Sodium Fluoride 39-54 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 29478513-2 2018 Although glycolysis inhibitors such as sodium fluoride (NaF) in combination with potassium oxalate (KOx) are currently used for overcoming this drawback, their efficacy for stabilizing blood glucose is seemingly limited, and probably lower than that of newer additives such as the citrate buffer. Glucose 191-198 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 29478513-2 2018 Although glycolysis inhibitors such as sodium fluoride (NaF) in combination with potassium oxalate (KOx) are currently used for overcoming this drawback, their efficacy for stabilizing blood glucose is seemingly limited, and probably lower than that of newer additives such as the citrate buffer. Citric Acid 281-288 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 29895165-6 2018 In addition, at a concentration of 25 and 50 mumol/l Kaempferol could significantly reduce the expression of inflammatory mediators such as tumor necrosis factor alpha (TNF-alpha), interleukin-8 (IL-8) and macrophage inflammatory protein 1 alpha (MIP-1alpha) in human promonocytic U937 cells-derived macrophages (dU937) in response to lipopolysaccharides (LPS) stimulation. kaempferol 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 29856363-9 2018 In addition, alanine aminotransferase elevation during PEG-IFN therapy and lower serum interleukin-8 level at the end of PEG-IFN treatment were also significantly associated with HBsAg reduction by 1 year after PEG-IFN treatment (P=0.038, P=0.044, respectively). peg-ifn 121-128 C-X-C motif chemokine ligand 8 Homo sapiens 87-100 29162452-5 2018 Enzyme-linked immunosorbent assay (ELISA) results demonstrated that DT-13 could suppress the TNF-alpha-induced upregulation of reactive oxygen species (ROS), tumor necrosis factor receptor (TNFR), interleukin-8 (IL-8), monocyte chemoattractant protein-1 (MCP-1) and nitric oxide in vivo dose-dependently and suppressed production of nitric oxide in vitro as shown by DAF-FMDA. DT-13 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 197-210 29162452-7 2018 Taken together, we speculate that DT-13 inhibits endothelium vascular inflammation through regulating nitric oxide production and the expression of ROS, TNFR, IL-8, MCP-1, which are associated with inflammation. DT-13 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 29162452-5 2018 Enzyme-linked immunosorbent assay (ELISA) results demonstrated that DT-13 could suppress the TNF-alpha-induced upregulation of reactive oxygen species (ROS), tumor necrosis factor receptor (TNFR), interleukin-8 (IL-8), monocyte chemoattractant protein-1 (MCP-1) and nitric oxide in vivo dose-dependently and suppressed production of nitric oxide in vitro as shown by DAF-FMDA. DT-13 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 29923797-9 2018 Tumors previously exposed to niraparib had activated the ERK1/2 and AKT-mTOR pathways that correlated with increased plasma levels of IL-8, MIF, EGF, uPA and IL-12. niraparib 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 29121426-9 2018 Immunohistochemistry revealed that xanthohumol inhibited Ki-67 expression, CD31-positive microvessel density, NF-kappaB p65 expression, and VEGF and IL-8 levels. xanthohumol 35-46 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 30024813-13 2018 This finding argues that IL-8/ERK/AKT signaling may be an evolutionary survival response to [SRA737 + niraparib]. SRA737 93-99 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 30024813-13 2018 This finding argues that IL-8/ERK/AKT signaling may be an evolutionary survival response to [SRA737 + niraparib]. niraparib 102-111 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 29900007-9 2018 A differential inflammatory/matrix signature emerged in anthracycline induced cardiomyopathy patients compared to normal including increased interleukin-8 and MMP levels. Anthracyclines 56-69 C-X-C motif chemokine ligand 8 Homo sapiens 141-154 29614502-8 2018 Salivary fluoride levels at 4, 6, and 26 h decreased at each time point and were generally significantly higher for 5% NaF and 5% NaF + TCP. Fluorides 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 119-122 29614502-8 2018 Salivary fluoride levels at 4, 6, and 26 h decreased at each time point and were generally significantly higher for 5% NaF and 5% NaF + TCP. Fluorides 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 29614502-0 2018 Fluoride Levels in Unstimulated Whole Saliva following Clinical Application of Different 5% NaF Varnishes. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 29614502-1 2018 The aim of this study was to evaluate the fluoride release from differently formulated 5% NaF varnishes into unstimulated whole saliva in vivo. Fluorides 42-50 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 29782597-14 2018 Moreover PET/CT is performed in 1.5 h while Bone SPECT requires at least 3.5 h. Conclusions: The 18F-Fluoride PET/CT procedure could be performed with 2.9 MBq/Kg (minimum 185 MBq, recommended at least 200 MBq) of 18F-NaF to minimize the effective radiation dose received, maintaining the quality of the scan. Fluoride ion f-18 97-109 C-X-C motif chemokine ligand 8 Homo sapiens 217-220 30308495-1 2018 BACKGROUND/AIMS: We investigated the combined toxic effect of sodium fluoride (NaF) and sulfur dioxide (SO2) on kidney morphological changes and DNA damage in male Wistar rats. Sodium Fluoride 62-77 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 29723847-8 2018 LPS treatment dose-dependently increased the pro-inflammatory cytokine, such as interleukin (IL)-8, whereas EGCG significantly reduced the LPS-stimulated IL-8 production. epigallocatechin gallate 108-112 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 29723847-10 2018 In particular, in the result from an RNA interference-mediated assay, our finding showed that silencing of Tollip resulted in abrogation of the inhibitory action of EGCG on LPS-induced production of pro-inflammatory mediators (inducible nitric oxide synthase-mediated NO/COX2, and IL-8) and activation of MAPKs and NF-kappaB signaling pathways. epigallocatechin gallate 165-169 C-X-C motif chemokine ligand 8 Homo sapiens 281-285 30513523-10 2018 MiR-15 mimics induced nuclear translocation of NF-kappaB p65 and upregulated the expression of IL-8 and IFN-gamma in colonic epithelial cells; these effects were reversed by an miR-15 inhibitor. mir-15 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 30513523-10 2018 MiR-15 mimics induced nuclear translocation of NF-kappaB p65 and upregulated the expression of IL-8 and IFN-gamma in colonic epithelial cells; these effects were reversed by an miR-15 inhibitor. mir-15 177-183 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 28984080-5 2018 Our results demonstrated that the expression level of interleukin (IL)-6 and IL-8 were decreased after exposure of GMI and the myofibroblast activities, including collagen gel contraction, migration, invasion, and wound healing abilities were inhibited as well. misonidazole-glutathione conjugate 115-118 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 29030692-8 2018 IL-8 was significantly increased in the IVBe + STTA group (p = 0.003) but the changes in the VEGF levels were smaller than in the IVBe group (p = 0.025). 3-Buten-2-one, 1,1,1-trifluoro-4-mercapto-4-(2-thienyl)- 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 29030692-9 2018 CONCLUSION: Intravitreal bevacizumab and subtenon triamcinolone injection reduces the VEGF, MCP-1 and PDGF-AA levels and increases the IL-8 level in the plural cytokine profiles of patients with DME, which might explain the limited therapeutic effect of combination therapy. Triamcinolone 50-63 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 29030692-9 2018 CONCLUSION: Intravitreal bevacizumab and subtenon triamcinolone injection reduces the VEGF, MCP-1 and PDGF-AA levels and increases the IL-8 level in the plural cytokine profiles of patients with DME, which might explain the limited therapeutic effect of combination therapy. dme 195-198 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 29649811-11 2018 Moreover, budesonide decreased CDK9 phosphorylation and markedly inhibited IL-17F-induced IL-8 production. Budesonide 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28113517-7 2018 Applying 1H-15N Heteronuclear Single Quantum Coherence NMR measurements, we determined the putative regions at IL-8 that are potentially responsible for interactions with the pepsin. Hydrogen 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 28113517-7 2018 Applying 1H-15N Heteronuclear Single Quantum Coherence NMR measurements, we determined the putative regions at IL-8 that are potentially responsible for interactions with the pepsin. 15n 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 29398016-15 2018 The allergens (Der p2 and Der p3)-induced IL-6/IL-8 expression and NCA released from Beas-2B could be downregulated by dexamethasone and transcription factor inhibitor SP600125. Dexamethasone 119-132 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 29398016-15 2018 The allergens (Der p2 and Der p3)-induced IL-6/IL-8 expression and NCA released from Beas-2B could be downregulated by dexamethasone and transcription factor inhibitor SP600125. pyrazolanthrone 168-176 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 29193173-4 2018 Further, LSCM can image sodium fluorescein (NaF) fluorescence with 488 nm excitation (fluorescence confocal microcopy (FCM)), a small hydrophilic test molecule (370 MW, log P -1.52), which may simulate uptake, bio-distribution and kinetics of small hydrophilic drugs. Fluorescein 24-42 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 29482476-6 2018 In addition, PFDA and PFUnA enhanced gene expression of pro-inflammatory cytokines, such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, IL-6, and IL-8 by activation of nuclear factor-kappaB in IgE-stimulated mast cells. perfluorodecanoic acid 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 30518712-2 2018 However, our previous study suggested the superiority of the modified IL-8 Luc assay (mIL-8 Luc), in which X-VIVOTM 15 is used to dissolve chemicals, over the original assay using DMSO (oIL-8 Luc). x-vivotm 15 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 29175450-6 2018 HCh-3 and LY294002 (alone or in combination) as well as Tiotropium (Spiriva ) or Olodaterol (alone or in combination) all reduced the levels of pPEBP1, pbeta2AR, pERK1/2, ROS, NOX-4, and IL-8 in 16HBE LECSE compared to untreated cells. hch-3 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 29175450-6 2018 HCh-3 and LY294002 (alone or in combination) as well as Tiotropium (Spiriva ) or Olodaterol (alone or in combination) all reduced the levels of pPEBP1, pbeta2AR, pERK1/2, ROS, NOX-4, and IL-8 in 16HBE LECSE compared to untreated cells. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 29175450-6 2018 HCh-3 and LY294002 (alone or in combination) as well as Tiotropium (Spiriva ) or Olodaterol (alone or in combination) all reduced the levels of pPEBP1, pbeta2AR, pERK1/2, ROS, NOX-4, and IL-8 in 16HBE LECSE compared to untreated cells. Tiotropium Bromide 56-66 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 28439952-10 2018 Higher levels of IL-6, IL-8 and TNF-alpha were found in cell supernatant after stimulation with multimethacrylate (Real Seal) compared to all other sealers tested (P < 0.05). multimethacrylate 96-113 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 29439331-9 2018 Higher CSF sAbetaPPbeta levels were associated with higher plasma markers only (IL-8; MCP-1). sabetappbeta 11-23 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 27818276-3 2018 Recent evidence shows that vitamin D acts to maintain the integrity of the gut mucosal barrier by enhancement of intercellular junctions that control mucosal permeability and reduction of pro-inflammatory cytokines such as IL-8. Vitamin D 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 28920187-6 2018 Five percent NaF varnish was used as fluoride preparate. fluoride preparate 37-55 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 29175450-6 2018 HCh-3 and LY294002 (alone or in combination) as well as Tiotropium (Spiriva ) or Olodaterol (alone or in combination) all reduced the levels of pPEBP1, pbeta2AR, pERK1/2, ROS, NOX-4, and IL-8 in 16HBE LECSE compared to untreated cells. Tiotropium Bromide 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 29193173-4 2018 Further, LSCM can image sodium fluorescein (NaF) fluorescence with 488 nm excitation (fluorescence confocal microcopy (FCM)), a small hydrophilic test molecule (370 MW, log P -1.52), which may simulate uptake, bio-distribution and kinetics of small hydrophilic drugs. Fosfomycin 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 29145158-6 2018 rOmpU-induced IL-8 expression was inhibited by interference of lipid raft formation with nystatin, but not by blocking the formation of clathrin-coated pits with chlorpromazine. Nystatin 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 29175450-6 2018 HCh-3 and LY294002 (alone or in combination) as well as Tiotropium (Spiriva ) or Olodaterol (alone or in combination) all reduced the levels of pPEBP1, pbeta2AR, pERK1/2, ROS, NOX-4, and IL-8 in 16HBE LECSE compared to untreated cells. olodaterol 81-91 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 29859938-9 2018 TvSP-induced migration, ROS generation, CD63 expression and IL-8 release were significantly suppressed by pretreatment with OGT inhibitor ST045849 or OGT siRNA. tvsp 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 29145158-3 2018 In this study, we evaluated the role of OmpU in induction of IL-8, a representative chemokine that recruits various inflammatory immune cells, in the human intestinal epithelial cell (IEC) line, HT-29. ompu 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 29145158-7 2018 In addition, rOmpU-induced IL-8 expression was mediated via ERK1/2 and p38 kinase pathways, but not via JNK signaling pathway. rompu 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 29051319-7 2018 When LoVo-P and HT29-C cells were cocultured with TAMs, CCL26 binding to the CCR3 receptor enhanced the invasiveness of LoVo-P and HT29-C cells by mobilizing intracellular Ca2+of TAMs to increase the expression of IL6 and IL8. Tamoxifen 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 222-225 29051319-7 2018 When LoVo-P and HT29-C cells were cocultured with TAMs, CCL26 binding to the CCR3 receptor enhanced the invasiveness of LoVo-P and HT29-C cells by mobilizing intracellular Ca2+of TAMs to increase the expression of IL6 and IL8. lovo-p 5-11 C-X-C motif chemokine ligand 8 Homo sapiens 222-225 29258450-10 2017 Patients who survived more than 2 years after sorafenib treatment exhibited higher serum levels of IL-10, IL-12, TNF-a, IL-8, SDF-1, EGF, PDGF-BB, SCF, and TGF-alpha. Sorafenib 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 29115434-7 2018 The addition of n-butanol extract from Folium isatidis inhibited this LPS-induced downregulation of CXCR1, CXCR2 and CD62L, and decreased the expression of IL-8 on neutrophils. 1-Butanol 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 29115448-8 2018 BDCM inhibited the inflammation-triggered production of cytokines including interleukin (IL)-6, IL-8, and tumor necrosis factor (TNF)-alpha. bromodichloromethane 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 29115448-12 2018 In conclusion, BDCM suppresses the expression of TNF-alpha, IL-8, and IL-6 by inhibiting the NF-kappaB and mitogen activated protein kinase signaling pathways. bromodichloromethane 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 29055264-7 2018 Venlafaxine treatment caused greater decreases in the levels of interferon gamma (IFN-gamma), tumor necrosis factor alpha (TNF-alpha), interleukin 4 (IL-4), IL-5, IL-1beta, and IL-8 than did paroxetine. Venlafaxine Hydrochloride 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 29375548-9 2017 Finally, we demonstrate that increased mitochondrial ROS enhanced phosphorylation of ERK1/2, and induced production of IL8, findings that correlate with previous observations of increased MAPK activation and inflammatory cytokine production in CGD cells. Reactive Oxygen Species 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 119-122 29145158-8 2018 Finally, V. cholerae lacking ompU elicited decreased IL-8 expression and adherence to HT-29 cells compared to the parental strain. ompu 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 31258241-12 2018 However, only the perovskite and CaIrO3 structures are stable with respect to dissociation into NaF and MgF2. perovskite 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 30116274-9 2018 The level of serum IL-8 was significant higher in patients with FE than that of patients with NFE (209.0 pg/mL (ranged: 115-472) vs 65.6 pg/mL (ranged: 11.2-149.3), P=0.008). Iron 64-66 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 30116274-9 2018 The level of serum IL-8 was significant higher in patients with FE than that of patients with NFE (209.0 pg/mL (ranged: 115-472) vs 65.6 pg/mL (ranged: 11.2-149.3), P=0.008). nfe 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 29348982-0 2017 Pictorial atlas of symptomatic accessory ossicles by 18F-Sodium Fluoride (NaF) PET-CT. Accessory ossicles are developmental variants which are often asymptomatic. 18f-sodium fluoride 53-72 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 29348982-4 2017 18F-Sodium Fluoride (NaF) is a PET imaging agent used in bone imaging. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 29262362-3 2017 Here, we describe 1H-detected magic angle spinning solid-state NMR studies of monomeric IL-8 (1-66) bound to full-length and truncated constructs of CXCR1 in phospholipid bilayers under physiological conditions. Hydrogen 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 29262362-3 2017 Here, we describe 1H-detected magic angle spinning solid-state NMR studies of monomeric IL-8 (1-66) bound to full-length and truncated constructs of CXCR1 in phospholipid bilayers under physiological conditions. Phospholipids 158-170 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 29262362-4 2017 Cross-polarization experiments demonstrate that most backbone amide sites of IL-8 (1-66) are immobilized and that their chemical shifts are perturbed upon binding to CXCR1, demonstrating that the dynamics and environments of chemokine residues are affected by interactions with the chemokine receptor. Amides 62-67 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 29258201-4 2017 Supplementation of the culture medium with particular fatty acids was found to have a promoting effect on cellular production of the cytokines IL-6, IL-8, GM-CSF, and MCP-1. Fatty Acids 54-65 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 29262362-6 2017 Intermolecular paramagnetic relaxation enhancement broadening of IL-8 (1-66) signals results from interactions of the chemokine with CXCR1 (1-350) containing Mn2+ chelated to an unnatural amino acid assists in the characterization of the receptor-bound form of the chemokine. Manganese(2+) 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 29260335-3 2017 It is found that the emission intensity of green and red light is enhanced for several times by the way of using NaBF4 as a fluoride source with the comparison of NH4F and NaF. Sodium tetrafluoroborate 113-118 C-X-C motif chemokine ligand 8 Homo sapiens 172-175 29236068-15 2017 To support the ability to inhibit p38 MAPK, the treatment of javamide-II-ethyl and -methyl esters could suppress the production of IL-8 and MCP-1 protein significantly by 22-73% (p < 0.05) in the differentiated THP-1 cells, and the inhibition was slightly stronger by the ethyl ester than the methyl ester. javamide-ii-ethyl and -methyl esters 61-97 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 29236068-15 2017 To support the ability to inhibit p38 MAPK, the treatment of javamide-II-ethyl and -methyl esters could suppress the production of IL-8 and MCP-1 protein significantly by 22-73% (p < 0.05) in the differentiated THP-1 cells, and the inhibition was slightly stronger by the ethyl ester than the methyl ester. ethyl ester 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 29236068-15 2017 To support the ability to inhibit p38 MAPK, the treatment of javamide-II-ethyl and -methyl esters could suppress the production of IL-8 and MCP-1 protein significantly by 22-73% (p < 0.05) in the differentiated THP-1 cells, and the inhibition was slightly stronger by the ethyl ester than the methyl ester. methyl ester 84-96 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 29207957-12 2017 At high percentiles of IL-1beta, IFN-gamma and IL-8, women with CDMR had higher expression levels compared to women with VD. cdmr 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 29416683-4 2018 In particular, H2O2-treated CCAR2-depleted cells showed a significant increase in interleukin-8 (IL-8) production, indicating a negative regulation of IL-8 by CCAR2. Hydrogen Peroxide 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 29416683-4 2018 In particular, H2O2-treated CCAR2-depleted cells showed a significant increase in interleukin-8 (IL-8) production, indicating a negative regulation of IL-8 by CCAR2. Hydrogen Peroxide 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 29416683-4 2018 In particular, H2O2-treated CCAR2-depleted cells showed a significant increase in interleukin-8 (IL-8) production, indicating a negative regulation of IL-8 by CCAR2. Hydrogen Peroxide 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 29228979-8 2017 RESULTS: We demonstrate that bryostatin-1 induces secretion of chemokines CCL2 and IL-8 and proinflammatory cytokines IL-6 and GM-CSF, whereas their production is repressed by JQ1. bryostatin 1 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 29207957-13 2017 Women with CDMI had higher levels at median percentiles of IL-1beta, IFN-gamma and IL-8. 2-(2-methyl-4-chlorophenylamino)-2-imidazoline 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 29207576-7 2017 Enzymatic GAG depolymerization via heparinase III and chondroitinase ABC was used to emulate the effect of glycocalyx remodeling on CXCL8-induced endothelial downstream signaling. Glycosaminoglycans 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 132-137 29207957-15 2017 It is worth noting that at high percentiles, compared with normal delivery, the expression of IL-1beta, IFN-gamma, IL-8 and HO-1 have significantly altered in women with CDMR. cdmr 170-174 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 29230430-10 2018 Conclusions: TEGDMA affects production of proinflammatory cytokines IL-1beta, IL-6, IL-8, IL-18 and TNF-alpha. triethylene glycol dimethacrylate 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 29213094-3 2017 In this study, we investigated the toxic effect of sodium fluoride (NaF) exposure on porcine oocyte maturation and its possible underlying mechanisms. Sodium Fluoride 51-66 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 29213094-7 2017 NaF exposure also induced oxidative stress, decreased GSH level, and increased cathepsin B activity in and impaired the further development potential of porcine oocytes, as indicated by a decrease in blastocyst formation rate, increase in apoptosis, and inhibition of cell proliferation. Glutathione 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 28976240-8 2017 H2O2 and LPS up-regulated IL-8. Hydrogen Peroxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 29058460-2 2017 In the present study, we demonstrated that ginsenoside Rg1 induced secretion of cytokines, including interleukin (IL)-6, tumor necrosis factor-alpha (TNF-alpha), and IL-1beta, and chemokines such as IL-8 and IP-10 in a dose-dependent manner by human peripheral blood mononuclear cell (PBMC)-derived dendritic cells. Ginsenosides 43-54 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 28210997-1 2017 BACKGROUND: Sodium fluoride (NaF) positron emission tomography combined with computer tomography (PET/CT) has shown to be more sensitive than the whole-body bone scan in the detection of skeletal uptake due to metastases in prostate cancer. Sodium Fluoride 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 28704260-6 2017 In vitro, we demonstrated, using cultured human PASMC from PAH patients, that alpha-solanine reversed dysfunctional AXIN2, beta-catenin and bone morphogenetic protein receptor type-2 signaling, whereas restored [Ca]i, IL-6 and IL-8, contributing to the decrease of PAH-PASMC proliferation and resistance to apoptosis. alpha-solanine 78-92 C-X-C motif chemokine ligand 8 Homo sapiens 227-231 29193074-4 2017 Using quantitative real-time polymerase chain reaction, we measure mRNA expression of pro-inflammatory cytokines: TNF-alpha, Interleukin (IL)-1beta, IL-6, and chemokine IL-8 under PA and 1alpha,25(OH)2 D3 influence. Palmitic Acid 180-182 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 28643937-7 2017 RESULTS: S100A9 and S100A8/A9 significantly upregulated IL-6 and IL-8 expression, which was inhibited upon treatment with the TLR4 inhibitor TAK242. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 141-147 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 27197820-3 2017 F-18 sodium fluoride (NaF) has been used to image inflammation in coronary artery plaques and has low background myocardial uptake. Sodium Fluoride 5-20 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 29285177-8 2017 The results demonstrated that after Simvastatin treatment of patients with acute cerebral hemorrhage at the ICU, the plasma concentrations of IL-4, IL-6, IL-8 and IL-10 were downregulated compared with those in placebo-treated controls. Simvastatin 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 29242736-0 2017 Inguinal Herniation of Urinary Bladder on F-18 Sodium Fluoride (NaF) PET-CT. Inguinal herniation of urinary bladder is uncommon and usually an incidental finding in asymptomatic patients. Fluorine-18 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 28953207-2 2017 Fluorine-18-sodium fluoride (F-NaF) PET-computed tomography (CT) has rapid single-pass extraction, fast clearance from the soft tissues and a better target to background ratio. fluorine-18-sodium fluoride 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 27894951-0 2017 A pilot study of CXCL8 levels in crystal proven gout patients during allopurinol treatment and their association with cardiovascular disease. Allopurinol 69-80 C-X-C motif chemokine ligand 8 Homo sapiens 17-22 27894951-3 2017 We hypothesized that the well-known cardiovascular protective effects of allopurinol could be related to effects of this drug on CXCL8 levels. Allopurinol 73-84 C-X-C motif chemokine ligand 8 Homo sapiens 129-134 28242869-8 2017 Peripheral monocyte response to lipopolysaccharide stimulation was lower in alcohol-dependent subjects compared with controls for the proinflammatory cytokines interleukin-6 and interleukin-8. Alcohols 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 178-191 29038158-6 2017 CFA treatment induced CXCL1 and interleukin-8 mRNA in BEAS-2B and primary human bronchial epithelial cells through activation of both TRPM8 and TRPV1. 3-chloro-4-fluoroaniline 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 29242735-2 2017 Achievements from F-18 NaF PET/CT are: higher sensitivity of positron imaging, higher target background ratio with higher tracer accumulation in bone hydroxyapatite and higher specificity through CT correlation. Durapatite 150-164 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 28065790-5 2017 Moreover, oxidative stress was evidenced only after exposure to CS, with a decrease secretion of GRO-alpha from 8min and of IL-8 and MCP-1 after 48min exposure. Cesium 64-66 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 29242736-0 2017 Inguinal Herniation of Urinary Bladder on F-18 Sodium Fluoride (NaF) PET-CT. Inguinal herniation of urinary bladder is uncommon and usually an incidental finding in asymptomatic patients. Sodium Fluoride 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 29083169-5 2017 All three astaxanthin isomers were effective in maintaining cellular redox homeostasis as seen in the antioxidant enzyme (CAT, SOD) activities ; 9Z- and 13Z- astaxanthins exhibited a higher protective effect than all-E-astaxanthin against oxidative stress as demonstrated by the lower cellular uptake of Z-astaxanthins and lower secretion and gene expression of the pro-inflammatory cytokine IL-8 in Caco-2 cells treated with H2O2. astaxanthine 10-21 C-X-C motif chemokine ligand 8 Homo sapiens 392-396 28987380-7 2017 Ex vivo incubation with quercetin in blood of both IPF patients and healthy controls reduces LPS-induced production of the pro-inflammatory cytokines IL-8 and TNFalpha. Quercetin 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 29083169-5 2017 All three astaxanthin isomers were effective in maintaining cellular redox homeostasis as seen in the antioxidant enzyme (CAT, SOD) activities ; 9Z- and 13Z- astaxanthins exhibited a higher protective effect than all-E-astaxanthin against oxidative stress as demonstrated by the lower cellular uptake of Z-astaxanthins and lower secretion and gene expression of the pro-inflammatory cytokine IL-8 in Caco-2 cells treated with H2O2. 9z- and 13z- astaxanthins 145-170 C-X-C motif chemokine ligand 8 Homo sapiens 392-396 29285315-7 2017 In indirect co-cultures, not only signal pathway inhibitors but also neutralizing antibodies against CXCL8, CXCR1 and CXCR2 suppressed these phenotypes induced by TAM-like PBMo-derived macrophages. tam 163-166 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 29172280-2 2017 SKOV3 cells displayed platinum-inducedIL-6 and IL-8 overproduction whereas wild type A2780 displayed no detectable cytokine production. Platinum 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 29172280-5 2017 However, carboplatin-induced IL-6 and IL-8 production had a significant association withthe clinical response to chemotherapy (P=0.016 and P=0.038 respectively). Carboplatin 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 29172280-6 2017 Carboplatin-induced IL-8 overproductionwas correlated with FIGO staging III-IV (P=0.026), but no correlation between carboplatin-induced IL-6 and FIGOstaging (P= 0.061) was noted. Carboplatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 29209219-2 2017 Signaling through p38MAPK, ERK, Rho kinase, and MSK-CREB contributes to LPA-mediated IL-8 production in fibroblast-like synoviocytes (FLS) from rheumatoid arthritis (RA) patients. lysophosphatidic acid 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 29209219-12 2017 In TNFalpha-primed RAFLS the super-production of IL-8 and IL-6 induced by LPA occurs mainly via MSK-independent pathways, and simultaneous inhibition of at least two MAPK signaling pathways was required to block their synthesis. lysophosphatidic acid 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 29209219-13 2017 Since simultaneous inhibition of both the p38MAPK and ERK-MSK-CREB pathways are required to significantly reduce LPA-mediated IL-8 and IL-6 production in TNFalpha-preconditioned RAFLS, drug combinations targeting these two pathways are potential new strategies to treat rheumatoid arthritis. lysophosphatidic acid 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 29178922-12 2017 LPA induced the release of IL-8 from ESCs but did not affect cell proliferation and VEGF production. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 29160802-9 2017 Contrariwise, the modification of the surface chemistry increased the apparent dielectric constant of NaF-water solution by promoting fluoride transmission. Water 106-111 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 29160802-9 2017 Contrariwise, the modification of the surface chemistry increased the apparent dielectric constant of NaF-water solution by promoting fluoride transmission. Fluorides 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 29312586-9 2017 Thus, glucose affects tamoxifen responsiveness directly modulating CTGF in BC cells, and indirectly promoting IL8 release by adipocytes. Glucose 6-13 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 29147010-8 2017 The effects of TDI exposure on FLCN production was investigated by treating HAECs (A549 cells) with TDI-human serum albumin conjugate, which showed increased expression and release of FLCN and interleukin-8 from HAECs. Toluene 2,4-Diisocyanate 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 193-206 29131834-7 2017 Pathway analysis of potential mRNAs targets of these miRNA revealed in the DLBCL group potential up-regulation of STAT3, IL8, p13k/AKT and TGF-B signaling, and potential down-regulation of the PTEN and p53 pathways; while in the HL group we have found the cAMP-mediated pathway and p53 pathway to be potentially down-regulated. Cyclic AMP 256-260 C-X-C motif chemokine ligand 8 Homo sapiens 121-124 28842514-10 2017 The poly(I:C)-induced release of inflammatory mediators, including CXCL8, interleukin (IL)-6 and CXCL1, from ASMCs from cough patients was significantly impaired compared with healthy non-cough subjects. poly 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 67-72 28842514-10 2017 The poly(I:C)-induced release of inflammatory mediators, including CXCL8, interleukin (IL)-6 and CXCL1, from ASMCs from cough patients was significantly impaired compared with healthy non-cough subjects. Iodine 9-10 C-X-C motif chemokine ligand 8 Homo sapiens 67-72 28842514-10 2017 The poly(I:C)-induced release of inflammatory mediators, including CXCL8, interleukin (IL)-6 and CXCL1, from ASMCs from cough patients was significantly impaired compared with healthy non-cough subjects. asmcs 109-114 C-X-C motif chemokine ligand 8 Homo sapiens 67-72 29750184-6 2018 Results: In samples from 14 patients we confirmed a strongly compartmentalized immune response at the disease site and found that prednisolone significantly reduced IL-6 concentrations in plasma by 8 hours of treatment, IL-1beta concentrations in saliva, as well as IL-8 concentrations in both pericardial fluid and saliva by 24 hours. Prednisolone 130-142 C-X-C motif chemokine ligand 8 Homo sapiens 266-270 29290940-0 2017 Lysophosphatidylcholine induces cytotoxicity/apoptosis and IL-8 production of human endothelial cells: Related mechanisms. Lysophosphatidylcholines 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 29290940-15 2017 LPC-induced apoptosis, and IL-8 expression/secretion was attenuated by LY294002, a PI3K/Akt inhibitor. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 29133478-1 2017 BACKGROUND: 18F-sodium fluoride (18F-NaF) positron-emission tomography has been introduced as a potential noninvasive imaging tool to identify plaques with high-risk characteristics in patients with coronary artery disease. 18f-sodium fluoride 12-31 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 29096855-9 2017 Moreover, excretion of IL-8 into the medium rapidly increased up to 1.7 +- 0.3 fold in response to treatment of ADSCs with DHA. Docosahexaenoic Acids 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 28866366-1 2017 Interleukin-8 (CXCL8) was originally described asa chemokine whose main function is the attraction of a polymorphonuclear inflammatory leukocyte infiltrate acting on CXCR1/2. Aspirin 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 28866366-1 2017 Interleukin-8 (CXCL8) was originally described asa chemokine whose main function is the attraction of a polymorphonuclear inflammatory leukocyte infiltrate acting on CXCR1/2. Aspirin 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 28866366-5 2017 Thus, IL-8 serum concentrations have been shown to be useful asa pharmacodynamic biomarker to early detect response to immunotherapy. Aspirin 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 29093275-4 2017 HuMax-IL8 was shown to revert mesenchymalization in claudin-low TNBC models both in vitro and in vivo as well as to significantly decrease the recruitment of polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) at the tumor site, an effect substantiated when used in combination with docetaxel. Docetaxel 294-303 C-X-C motif chemokine ligand 8 Homo sapiens 0-9 28852782-1 2017 An ultrasensitive surface-enhanced Raman scattering (SERS) immunoassay based on diatom biosilica with integrated gold nanoparticles (AuNPs) for the detection of interleukin 8 (IL-8) in blood plasma has been developed. sers 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 28852782-1 2017 An ultrasensitive surface-enhanced Raman scattering (SERS) immunoassay based on diatom biosilica with integrated gold nanoparticles (AuNPs) for the detection of interleukin 8 (IL-8) in blood plasma has been developed. sers 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 28852782-8 2017 To the best of our knowledge, this is the first report on the recognition of IL-8 in human samples using a SERS-based method. sers 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 28852782-11 2017 This SERS immunoassay also exhibits high biological specificity for the detection of IL-8 antigens. sers 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 28852782-13 2017 Graphical Abstract The SERS-based immunoassay based on naturally generated photonic biosilica for the detection of interleukin 8 (IL-8) in human plasma samples. sers 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 28852782-13 2017 Graphical Abstract The SERS-based immunoassay based on naturally generated photonic biosilica for the detection of interleukin 8 (IL-8) in human plasma samples. sers 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 28012895-2 2017 The cells were treated with sodium fluoride (NaF) alone and in combination with PCAME for different time points (0-24 h) and evaluated for intracellular reactive oxygen species (ROS) production, F- content, oxidative stress markers, apoptosis and mRNA expression of redox signaling and inflammatory genes. Sodium Fluoride 28-43 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 28872551-0 2017 Diagnostic Challenge of Staging Metastatic Bone Disease in the Morbidly Obese Patients: A Primary Study Evaluating the Usefulness of 18F-Sodium Fluoride (NaF) PET-CT. PURPOSE: Optimizing diagnostic imaging may be challenging in obese patients. 18f-sodium fluoride 133-152 C-X-C motif chemokine ligand 8 Homo sapiens 154-157 28872551-2 2017 In comparison, sodium fluoride (F-NaF PET-CT) has a better target-to-background ratio attributed to rapid single-pass extraction and fast clearance from the soft tissues. Sodium Fluoride 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 28872551-3 2017 The aim of the present study is to assess the diagnostic efficacy of F-NaF PET-CT in the evaluation of bone metastases in obese cancer patients. Fluorine 69-70 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 26663823-9 2017 The GSH/GSSG ratio negatively correlated with IL-6 (P: 0.014), IL-8 (P: 0.014) and IL-10 (P: 0.033). Glutathione Disulfide 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 26663823-9 2017 The GSH/GSSG ratio negatively correlated with IL-6 (P: 0.014), IL-8 (P: 0.014) and IL-10 (P: 0.033). Glutathione Disulfide 8-12 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 28901414-6 2017 Brassinin treatment also markedly decreased the mRNA expression levels of interleukin-8 in a dose-dependent manner. brassinin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 28736998-0 2017 Evasin-displaying lactic acid bacteria bind different chemokines and neutralize CXCL8 production in Caco-2 cells. Lactic Acid 18-29 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 28901435-7 2017 The nuclear factor-kappaB inhibitor, Bay 11-7082, decreased the TNF-alpha-mediated expression of IL-8 and CXCL10 in the absence, and presence of IFN-gamma. 3-(4-methylphenylsulfonyl)-2-propenenitrile 37-48 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 28912098-2 2017 Melatonin, an indolamine synthesized in the pineal gland, was previously shown to protect against sodium fluoride (NaF)-induced hepatotoxicity. Melatonin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 28912098-2 2017 Melatonin, an indolamine synthesized in the pineal gland, was previously shown to protect against sodium fluoride (NaF)-induced hepatotoxicity. indolamine 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 28912098-2 2017 Melatonin, an indolamine synthesized in the pineal gland, was previously shown to protect against sodium fluoride (NaF)-induced hepatotoxicity. Sodium Fluoride 98-113 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 28912098-3 2017 This study investigated the protective effects of melatonin pretreatment on NaF-induced hepatotoxicity and elucidates the potential mechanism of melatonin-mediated protection. Melatonin 50-59 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 28912098-4 2017 Reducing mitochondrial ROS by melatonin substantially attenuated NaF-induced NADPH oxidase 4 (Nox4) upregulation and cytotoxicity in L-02 cells. Reactive Oxygen Species 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 28912098-4 2017 Reducing mitochondrial ROS by melatonin substantially attenuated NaF-induced NADPH oxidase 4 (Nox4) upregulation and cytotoxicity in L-02 cells. Melatonin 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 28912098-11 2017 Our findings provided a theoretical basis that melatonin mitigated NaF-induced hepatotoxicity, which, in part, was mediated through the activation of the Sirt3 pathway. Melatonin 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 28657808-9 2017 Among the fluoride compounds, NaF was mentioned more frequently than SnF2, Na2PO3F, amine fluoride, and acidulated phosphate fluoride during the years 1986 to 2015. Fluorides 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 28798033-11 2017 Conclusion:18F-NaF PET/CT and whole-body SPECT/CT resulted in a significant reduction of equivocal readings compared with pBS, which implies an improved diagnostic confidence. pbs 122-125 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 28849160-4 2017 The results indicated that GBP and PGB suppressed the SP-induced production of IL-6, and IL-8 in U373 MG cells. Pregabalin 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 28849160-6 2017 Together, these observations suggest that GBP and PGB likely prevent SP-induced IL-6 and IL-8 production in U373 MG cells via the inhibition of signaling molecules, including p38 MAPK and NF-kappaB, thereby exhibiting antineuroinflammatory effects. Pregabalin 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 29068698-4 2017 Polyphenols influence the inflammatory process by controlling and inhibiting pro-inflammatory cytokines such as IL-1beta, IL-6, IL-8, and TNF-alpha, and cyclooxygenase-2 (COX-2) enzyme involved in the metabolism of arachidonic acid. Polyphenols 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 28877084-1 2017 OBJECTIVE: Coronary artery fluorine-18-sodium fluoride (F-NaF) uptake reflects coronary artery calcification metabolism and is considered to be an early prognostic marker of coronary heart disease. fluorine-18-sodium fluoride 27-54 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 28865757-7 2017 Only the highest concentration tested of L-AmB (400mug/ml) yielded transient significant 6-fold and 4-fold induction of TNF-alpha and IL-8 mRNAs, respectively. liposomal amphotericin B 41-46 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 28494217-5 2017 The IL-8 concentration determined on day 1 was significantly negatively correlated with creatinine clearance early after renal transplantation (on days 1, 7, 14 and 30), as well as during long-term observations. Creatinine 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 28865757-9 2017 Significant 4-fold, 7-fold and 3-fold inductions of TNF-alpha, IL-8 and IL-33 mRNAs were also observed at 6h with 50mug/ml of D-AmB. Deoxycholate-AmB 126-131 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 28766731-13 2017 Levels of CXCL-8 (C-X-C motif chemokine ligand 1) and interleukin-6 were significantly higher after treatment with RMPs. rmps 115-119 C-X-C motif chemokine ligand 8 Homo sapiens 10-16 29168724-2 2017 Thermodynamic analysis of four possible additives, Na2CO3, Na2C2O4, NaF and Na2SO4, indicated that both carbonate and oxalate could potentially provide effective separation of Ca via precipitation from Mg in FGD wastewater. Carbonates 104-113 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 29168724-2 2017 Thermodynamic analysis of four possible additives, Na2CO3, Na2C2O4, NaF and Na2SO4, indicated that both carbonate and oxalate could potentially provide effective separation of Ca via precipitation from Mg in FGD wastewater. Oxalates 118-125 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 28883082-4 2017 In our study, we found that CXCL8 was highly expressed in cervical cancer tissues compared with normal cervical tissues in microarray datasets (GSE9750 and GSE7803). gse9750 144-151 C-X-C motif chemokine ligand 8 Homo sapiens 28-33 29085059-9 2017 However, KL excess via overexpression or supplementation decreased IL-8 secretion by inhibiting Smad 3 phosphorylation. Kraft lignin 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 28823917-2 2017 To examine an alternative approach of integrin-based anti-osteosacoma strategy, acurhagin-C, a Glu-Cys-Asp (ECD)-disintegrin, was isolated and evaluated for its application in combination with two potent inhibitors of basic fibroblast growth factor (bFGF) and interleukin-8 (IL-8). acurhagin-c 80-91 C-X-C motif chemokine ligand 8 Homo sapiens 260-273 28823917-2 2017 To examine an alternative approach of integrin-based anti-osteosacoma strategy, acurhagin-C, a Glu-Cys-Asp (ECD)-disintegrin, was isolated and evaluated for its application in combination with two potent inhibitors of basic fibroblast growth factor (bFGF) and interleukin-8 (IL-8). acurhagin-c 80-91 C-X-C motif chemokine ligand 8 Homo sapiens 275-279 28899503-10 2017 RESULTS: Under non-inflammatory conditions P. tremula E and ASA increased cellular proteins (P) IL-8 and IL-10; S. virgaurea E modulated IL-1alpha, IL-10, IL-15 and Groalpha (P). Aspirin 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 28899503-16 2017 Secretion of IL-8 and IL-6 was reduced by STW1 and ASA. Aspirin 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 28883082-4 2017 In our study, we found that CXCL8 was highly expressed in cervical cancer tissues compared with normal cervical tissues in microarray datasets (GSE9750 and GSE7803). gse7803 156-163 C-X-C motif chemokine ligand 8 Homo sapiens 28-33 28836077-7 2017 CONCLUSIONS: Patients with T2D display a marked elevation of circulating IL-8 levels which identify subjects with worse inflammatory, glycometabolic and lipid profile and lower vitamin D levels. Vitamin D 177-186 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 28986583-6 2017 Nicotine at 10 micromol/L significantly downregulated the release of TNF-alpha, but showed a lesser effect on IL-8 secretion and no effect on TGF-beta. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 28864214-4 2017 Moreover, levels of serum miR-218 positively correlated with FEV1/FVC% and negatively correlated with levels of serum IL-6 and IL-8. mir-218 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 28976943-9 2017 High glucose-induced secretion of IL-8, TNF-alpha, ICAM-1, and VCAM-1 was reduced, and translocation of the p65 subunit of NF-kappaB to the endothelial cell nucleus was inhibited by EOFAZ. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 28860213-1 2017 Our aim was to prospectively evaluate the relationship between low back pain-related disability and quantitative measures from [18F]-sodium fluoride ([18F]-NaF) MR imaging. [18f]-sodium fluoride 127-148 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 28701056-7 2017 Treatment of IL-1beta stimulated fibroblasts in combination with PHMG-P or CHX at concentrations of 0.000045 or 0.0.00009% resulted in significantly decreased PGE2, IL-6, IL-8 and MMP-1 levels. polyhexamethyleneguanidine 65-71 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 28701056-7 2017 Treatment of IL-1beta stimulated fibroblasts in combination with PHMG-P or CHX at concentrations of 0.000045 or 0.0.00009% resulted in significantly decreased PGE2, IL-6, IL-8 and MMP-1 levels. Chlorhexidine 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 28860213-5 2017 These data suggest that dynamic [18F]-NaF PET may serve as a useful biomarker for facetogenic disability. Fluorine-18 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 28928970-9 2017 While UA significantly inhibited NO expression with time course- and dose- dependent manner in the cultured ECs, 10 mg/dl UA also increased expression of inflammation cytokine interleukin (IL)-6, IL-8 and tumor necrosis factor-alpha in vitro. Uric Acid 122-124 C-X-C motif chemokine ligand 8 Homo sapiens 196-232 28601733-0 2017 Effect of 1.2% of simvastatin gel as a local drug delivery system on Gingival Crevicular Fluid interleukin-6 & interleukin-8 levels in non surgical treatment of chronic periodontitis patients. Simvastatin 18-29 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 28601733-1 2017 AIM: The present study was carried out to evaluate the effect of 1.2% simvastatin gel as local drug delivery (LDD) system on Gingival Crevicular Fluid (GCF) Interleukin -6 (IL-6) and Interleukin-8 (IL-8) levels in chronic periodontitis patients, in addition to scaling and root planing (SRP). Simvastatin 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 183-196 28601733-1 2017 AIM: The present study was carried out to evaluate the effect of 1.2% simvastatin gel as local drug delivery (LDD) system on Gingival Crevicular Fluid (GCF) Interleukin -6 (IL-6) and Interleukin-8 (IL-8) levels in chronic periodontitis patients, in addition to scaling and root planing (SRP). Simvastatin 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 28892713-7 2017 SA also impairs CAC function and increases pro-inflammatory molecule (IL-1beta, IL-6, IL-8, MCP-1 and TNFalpha) gene expression and secretion in CACs starting from 3 h of incubation. stearic acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 29084500-12 2017 Driving pressures >= 19 cmH2O before ECMO were associated with higher IL8 levels. cmh2o 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 28550976-7 2017 The effect of anti-proliferative agent Mitomycin C upon secretion of pro-inflammatory cytokines IL-6 and IL-8 was assessed. Mitomycin 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 28966687-8 2017 A significant positive correlation was identified between the neutrophil polys and expression levels of four of these candidate genes, including CXCL2, IL8, TRIM58, and IGSF3 (all P<0.01; R2>=0.64). polys 73-78 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 28512018-6 2017 Moreover, NC-DFZ reduced the lipopolysaccharide (LPS) mediated secretion of the inflammatory marker IL-8. nc-dfz 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 28849137-5 2017 Furthermore, NW-PM2.5 and W-PM2.5 significantly reduced sebaceous lipid synthesis and markedly promoted the production of inflammatory cytokines, including interleukin-1alpha (IL-1alpha), IL-6 and IL-8 in SZ95 sebocytes. nw-pm2 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 28730511-0 2017 Intermediate Molecular Mass Hyaluronan and CD44 Receptor Interactions Enhance Neutrophil Phagocytosis and IL-8 Production via p38- and ERK1/2-MAPK Signalling Pathways. Hyaluronic Acid 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 28849137-5 2017 Furthermore, NW-PM2.5 and W-PM2.5 significantly reduced sebaceous lipid synthesis and markedly promoted the production of inflammatory cytokines, including interleukin-1alpha (IL-1alpha), IL-6 and IL-8 in SZ95 sebocytes. w-pm2 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 28109921-1 2017 OBJECTIVES: The aims of this study were to describe the authors" initial experience with combined coronary artery positron emission tomographic (PET) and magnetic resonance (MR) imaging using 18F-fluorodeoxyglucose (18F-FDG) and 18F-sodium fluoride (18F-NaF) radiotracers, describe common problems and their solutions, and demonstrate the feasibility of coronary PET/MR imaging in appropriate patients. Fluorodeoxyglucose F18 192-214 C-X-C motif chemokine ligand 8 Homo sapiens 254-257 29058282-8 2017 4-PBA significantly reduced the expression of CXCL-8 protein (P<0.05) and neutrophil migration (P<0.05). 4-phenylbutylamine 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 46-52 28743324-3 2017 Triptolide pretreatment significantly inhibited tumor necrosis factor-alpha-induced expression of the interleukin (IL)-1beta, IL-6, and IL-8 genes in MH7A cells. triptolide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 29055398-3 2017 While corticosteroid therapy is currently the recommended treatment for HSP, dapsone, an anti-leprosy agent, has also recently been suggested to have therapeutic efficacy due to its ability to suppress IL-8. Dapsone 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 29132841-6 2017 Pg-3-glc and PGA at 0.08 mumol/L increased the concentration of IL-10 (P<.01 and P<.001, respectively), but there was no effect on tumor necrosis factor-alpha, IL-1beta, IL-6, and IL-8, and there were no effects of the other compounds. pelargonidin-3-glucoside 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 28691370-7 2017 Subsequent experiment using an inflamed Caco-2 BBe1/THP-1 co-culture cell model showed these transported anthocyanins inhibited IL-8 and TNF-alpha secretion,and expression of pro-inflammatory cytokines by blocking NF-kappaB, and MAPK mediated inflammatory cellular signaling cascades, but with varying degrees due to structural features. Anthocyanins 105-117 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 28427103-10 2017 Kaempferol-3-O-sophoroside (10-50 microM), but not saffron flower acetone extract, inhibited TNF-alpha-induced IL-8 secretion. kaempferol 3-O-sophoroside 0-26 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 29132841-6 2017 Pg-3-glc and PGA at 0.08 mumol/L increased the concentration of IL-10 (P<.01 and P<.001, respectively), but there was no effect on tumor necrosis factor-alpha, IL-1beta, IL-6, and IL-8, and there were no effects of the other compounds. Folic Acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 28777220-0 2017 Normal bone and soft tissue distribution of fluorine-18-sodium fluoride and artifacts on 18F-NaF PET/CT bone scan: a pictorial review. fluorine-18-sodium fluoride 44-71 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 28777220-1 2017 Fluorine-18-sodium fluoride (F-NaF) PET/CT is a relatively new and high-resolution bone imaging modality. fluorine-18-sodium fluoride 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 28929009-13 2017 Furthermore, the results showed that IL-7, IL-8, IL-10, TGF-b, and VEGFR2 display peak differences between DF and SDI during or before the critical phase (day 4-5) of SDI. sdi 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 28823947-17 2017 Moreover, inhalation of GSK2269557 resulted in suppression of sputum IL-8 and IL-6 levels, consistent with the known anti-inflammatory activity of a PI3Kdelta inhibitor. gsk2269557 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 29033853-9 2017 Results: The major findings of these analyses were: (1) MCs secreted HMGB1 from the nucleus during exposure to high glucose levels; HMGB1 acted in an autocrine fashion on the MCs to promote the production of MCP-1 and IL-8; (2) HMGB1 had little effect on high-glucose-induced apoptosis of the MCs; and (3) HMGB1-mediated MCP-1 and IL-8 production depended on the activation of MAPK signaling pathways. mcs 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 29033853-9 2017 Results: The major findings of these analyses were: (1) MCs secreted HMGB1 from the nucleus during exposure to high glucose levels; HMGB1 acted in an autocrine fashion on the MCs to promote the production of MCP-1 and IL-8; (2) HMGB1 had little effect on high-glucose-induced apoptosis of the MCs; and (3) HMGB1-mediated MCP-1 and IL-8 production depended on the activation of MAPK signaling pathways. mcs 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 331-335 29033853-9 2017 Results: The major findings of these analyses were: (1) MCs secreted HMGB1 from the nucleus during exposure to high glucose levels; HMGB1 acted in an autocrine fashion on the MCs to promote the production of MCP-1 and IL-8; (2) HMGB1 had little effect on high-glucose-induced apoptosis of the MCs; and (3) HMGB1-mediated MCP-1 and IL-8 production depended on the activation of MAPK signaling pathways. mcs 175-178 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 29033853-9 2017 Results: The major findings of these analyses were: (1) MCs secreted HMGB1 from the nucleus during exposure to high glucose levels; HMGB1 acted in an autocrine fashion on the MCs to promote the production of MCP-1 and IL-8; (2) HMGB1 had little effect on high-glucose-induced apoptosis of the MCs; and (3) HMGB1-mediated MCP-1 and IL-8 production depended on the activation of MAPK signaling pathways. mcs 175-178 C-X-C motif chemokine ligand 8 Homo sapiens 331-335 29033853-9 2017 Results: The major findings of these analyses were: (1) MCs secreted HMGB1 from the nucleus during exposure to high glucose levels; HMGB1 acted in an autocrine fashion on the MCs to promote the production of MCP-1 and IL-8; (2) HMGB1 had little effect on high-glucose-induced apoptosis of the MCs; and (3) HMGB1-mediated MCP-1 and IL-8 production depended on the activation of MAPK signaling pathways. mcs 175-178 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 29033853-9 2017 Results: The major findings of these analyses were: (1) MCs secreted HMGB1 from the nucleus during exposure to high glucose levels; HMGB1 acted in an autocrine fashion on the MCs to promote the production of MCP-1 and IL-8; (2) HMGB1 had little effect on high-glucose-induced apoptosis of the MCs; and (3) HMGB1-mediated MCP-1 and IL-8 production depended on the activation of MAPK signaling pathways. mcs 175-178 C-X-C motif chemokine ligand 8 Homo sapiens 331-335 28929009-14 2017 DISCUSSION: This meta-analysis suggests that IL-7, IL-8, IL-10, TGF-b, and VEGFR2 may be used as potential early laboratory biomarkers in the diagnosis of SDI. sdi 155-158 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 28820234-1 2017 We developed a method of chemically welding silver nanowires (AgNWs) using an aqueous solution containing sodium halide salts (NaF, NaCl, NaBr, or NaI). sodium halide salts 106-125 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 28891967-7 2017 Ginsenoside Rg3 (10 mug/mL) effectively suppressed the expressions of IL-6 and IL-8, which is associated with regulations of NF-kappaB and p38MAPK activation. Ginsenosides 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 28878123-5 2017 SOD mimetic (Mn (III) tetrakis (N-ethylpyridinium-2-yl) porphyrin) attenuated Alternaria-induced expression of IL-33 and IL-8 release in BEAS-2B cells. mn (iii) tetrakis (n-ethylpyridinium-2-yl) porphyrin 13-65 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 29254155-4 2017 Casticin decreased levels of IL-6, tumor necrosis factor alpha, and IL-8 and suppressed COX-2 expression and prostaglandin E2 production. casticin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 28650029-8 2017 The present study shows that the amine-modified MSNs could encapsulate BA and BE, and nano-encapsulation greatly enhances the drug delivery rate and prolongs the release of BA and BE up to 216 h. Moreover, both Nano-BA and Nano-BE could be internalized by hGECs and retained intracellularly in nanoparticle-free media for at least 24 h. Note that Nano-BE pre-treatment effectively down-regulates the IL-1beta-induced expression of IL-6 and IL-8 in hGECs. Amines 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 440-444 28736978-1 2017 Chemokine cysteine-X-cysteine motif ligand 8 (CXCL8) is up-regulated in many malignancies, indicating that CXCL8 takes part in tumor progression. cysteine-x-cysteine 10-29 C-X-C motif chemokine ligand 8 Homo sapiens 46-51 28869519-6 2017 A cleft containing the predicted sulfotyrosine-binding pocket was identified as a principal hot spot for ligand binding on the structures of CXCL1, CXCL2, CXCL7, and CXCL8, but not CXCL5. tyrosine O-sulfate 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 28869519-7 2017 Sulfotyrosine titrations monitored via NMR spectroscopy showed specific binding to CXCL8, but not to CXCL5, which is consistent with the predictions from the computational solvent mapping. tyrosine O-sulfate 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 28869519-8 2017 The lack of CXCL5-sulfotyrosine interaction and the presence of CXCL8-sulfotyrosine binding suggests a role for receptor post-translational modifications regulating ligand selectivity. tyrosine O-sulfate 70-83 C-X-C motif chemokine ligand 8 Homo sapiens 64-69 28736978-1 2017 Chemokine cysteine-X-cysteine motif ligand 8 (CXCL8) is up-regulated in many malignancies, indicating that CXCL8 takes part in tumor progression. cysteine-x-cysteine 10-29 C-X-C motif chemokine ligand 8 Homo sapiens 107-112 28412861-7 2017 The change in IL8 mRNA was negatively associated with AR expression in the presence of NETA. Norethindrone Acetate 87-91 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 28111709-1 2017 Sodium fluoride (NaF) is a source of fluoride ions used in many applications. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 28111709-1 2017 Sodium fluoride (NaF) is a source of fluoride ions used in many applications. Fluorides 7-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 28111709-12 2017 Further, the fluorescence intensities of ROS in the NaF groups were higher than those in the control group, and the membrane potential of mitochondria in the NaF group was significantly lower than that of the control group (P < 0.05). ros 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 28700977-6 2017 Hypoxia-induced Tumor Necrosis Factor-alpha (TNF-alpha), Interleukin 6 (IL-6), and Interleukin 8 (IL-8) release were significantly reduced in the neferine pretreated samples indicating its anti-inflammatory role. neferine 146-154 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 28700977-6 2017 Hypoxia-induced Tumor Necrosis Factor-alpha (TNF-alpha), Interleukin 6 (IL-6), and Interleukin 8 (IL-8) release were significantly reduced in the neferine pretreated samples indicating its anti-inflammatory role. neferine 146-154 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 28437599-7 2017 The ASMCs were cultured with HBD-3 for 24 hour, and then the supernatant level of IL-8 was evaluated by ELISA and the cell viability was examined by WST-1 assay. asmcs 4-9 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 28437599-12 2017 Mitochondrial ROS regulated both HBD-3-induced IL-8 production and cell apoptosis. ros 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 28738247-7 2017 In vivo, asiatic acid significantly inhibited LPS-induced IL-6 and IL-8 expression levels in gingival tissues. asiatic acid 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 28738247-8 2017 In vitro, LPS-induced PGE2, NO, IL-6, and IL-8 production was significantly attenuated by asiatic acid. asiatic acid 90-102 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 28692879-3 2017 The results showed that pitavastatin inhibited the expression of inflammatory mediators IL-6 and IL-8. pitavastatin 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 28738247-11 2017 Furthermore, GW9662, a PPAR-gamma inhibitor, attenuated the inhibitory effect of asiatic acid on PGE2, NO, IL-6, and IL-8 production. 2-chloro-5-nitrobenzanilide 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 28692879-6 2017 These findings suggest that the mechanism underlying the inhibitory effects of pitavastatin on IL-1beta-induced IL-6 and IL-8 release might be mediated by the suppression of mitogen-activated protein kinase (MAPK), Akt, and nuclear factor-kappaB (NF-kappaB) signaling pathways. pitavastatin 79-91 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 28738247-11 2017 Furthermore, GW9662, a PPAR-gamma inhibitor, attenuated the inhibitory effect of asiatic acid on PGE2, NO, IL-6, and IL-8 production. asiatic acid 81-93 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 28883755-3 2017 Here, we demonstrate that hypoxia, reactive oxygen species (ROS), and differential concentration of glucose influence the expression of cytokines and chemokines, such as IL-6, IL-8, and IP-10, in human glial cell lines. Reactive Oxygen Species 35-58 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 28713941-5 2017 Celecoxib and simvastatin alone as well as a combined treatment showed a significant reduction in tumor cell viability, proliferation and secretion of IL-6 and IL-8 compared to the control group. Celecoxib 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 28713941-5 2017 Celecoxib and simvastatin alone as well as a combined treatment showed a significant reduction in tumor cell viability, proliferation and secretion of IL-6 and IL-8 compared to the control group. Simvastatin 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 28547650-9 2017 Exposure to Leu-Leu-OMe significantly promoted the production of IL-6 and IL-8 in primed HUVECs; this effect was prevented by the pre-treatment of cells with an IL-1RA. leucyl-leucine-methyl ester 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 28764952-0 2017 Prospective comparison of 18F-NaF PET/CT versus 18F-FDG PET/CT imaging in mandibular extension of head and neck squamous cell carcinoma with dedicated analysis software and validation with surgical specimen. Fluorine-18 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 28247965-0 2017 Lithocholic Acid Stimulates IL-8 Expression in Human Colorectal Cancer Cells Via Activation of Erk1/2 MAPK and Suppression of STAT3 Activity. Lithocholic Acid 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 28247965-3 2017 However, the effect of LCA on IL-8 expression is still undefined. Lithocholic Acid 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 28247965-4 2017 In this study, we observed that LCA treatment induced IL-8 expression in CRC HCT116 cells. Lithocholic Acid 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 28247965-5 2017 Pharmacological inhibition and mutagenesis studies indicated that Erk1/2 is critical for LCA-induced IL-8 expression. Lithocholic Acid 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 28247965-6 2017 Furthermore, LCA reduced the phosphorylation of STAT3, and the STAT3 inhibitor Stattic, accelerated LCA-induced IL-8 expression, suggesting that STAT3 is involved in LCA-induced IL-8 expression. Lithocholic Acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 28247965-6 2017 Furthermore, LCA reduced the phosphorylation of STAT3, and the STAT3 inhibitor Stattic, accelerated LCA-induced IL-8 expression, suggesting that STAT3 is involved in LCA-induced IL-8 expression. Lithocholic Acid 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 28247965-6 2017 Furthermore, LCA reduced the phosphorylation of STAT3, and the STAT3 inhibitor Stattic, accelerated LCA-induced IL-8 expression, suggesting that STAT3 is involved in LCA-induced IL-8 expression. Lithocholic Acid 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 28247965-6 2017 Furthermore, LCA reduced the phosphorylation of STAT3, and the STAT3 inhibitor Stattic, accelerated LCA-induced IL-8 expression, suggesting that STAT3 is involved in LCA-induced IL-8 expression. Lithocholic Acid 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 28247965-6 2017 Furthermore, LCA reduced the phosphorylation of STAT3, and the STAT3 inhibitor Stattic, accelerated LCA-induced IL-8 expression, suggesting that STAT3 is involved in LCA-induced IL-8 expression. Lithocholic Acid 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 28247965-8 2017 In conclusion, LCA activated Erk1/2 and in turn, suppressed STAT3 phosphorylation to induce IL-8 expression in HCT116 cells, thus stimulating endothelial cell proliferation and tube like formation. Lithocholic Acid 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 28883755-3 2017 Here, we demonstrate that hypoxia, reactive oxygen species (ROS), and differential concentration of glucose influence the expression of cytokines and chemokines, such as IL-6, IL-8, and IP-10, in human glial cell lines. Reactive Oxygen Species 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 28652177-0 2017 Inhibition of IL-6 and IL-8 production in LPS-stimulated human gingival fibroblasts by glycyrrhizin via activating LXRalpha. Glycyrrhizic Acid 87-99 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 28883755-3 2017 Here, we demonstrate that hypoxia, reactive oxygen species (ROS), and differential concentration of glucose influence the expression of cytokines and chemokines, such as IL-6, IL-8, and IP-10, in human glial cell lines. Glucose 100-107 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 28652177-5 2017 The results showed that glycyrrhizin significantly inhibited LPS-induced IL-6 and IL-8 production, as well as COX-2 and iNOS expression. Glycyrrhizic Acid 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 28652177-8 2017 In addition, the inhibition of glycyrrhizin on IL-6 and IL-8 production was reversed by LXRalpha inhibitor GGPP. Glycyrrhizic Acid 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 28883755-4 2017 Treatment with cobalt chloride (CoCl2) and hydrogen peroxide (H2O2) significantly increased the expression levels of IL-6, IL-8, and IP-10 in a dose-dependent manner in CRT-MG and U251-MG astroglioma cells, but not in microglia cells. cobaltous chloride 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 28883755-4 2017 Treatment with cobalt chloride (CoCl2) and hydrogen peroxide (H2O2) significantly increased the expression levels of IL-6, IL-8, and IP-10 in a dose-dependent manner in CRT-MG and U251-MG astroglioma cells, but not in microglia cells. cobaltous chloride 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 28883755-4 2017 Treatment with cobalt chloride (CoCl2) and hydrogen peroxide (H2O2) significantly increased the expression levels of IL-6, IL-8, and IP-10 in a dose-dependent manner in CRT-MG and U251-MG astroglioma cells, but not in microglia cells. Hydrogen Peroxide 43-60 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 28883755-4 2017 Treatment with cobalt chloride (CoCl2) and hydrogen peroxide (H2O2) significantly increased the expression levels of IL-6, IL-8, and IP-10 in a dose-dependent manner in CRT-MG and U251-MG astroglioma cells, but not in microglia cells. Hydrogen Peroxide 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 28713935-10 2017 ELISA analysis demonstrated that curcumin reduced PM2.5-induced oxLDL, TNF-alpha and IL-8 levels. Curcumin 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 28161237-5 2017 Here we report that LMWHs induce a profound change in the ability of human neutrophils to generate NETs and to mobilize the content of the primary granules in response to unrelated inflammatory stimuli, such as IL-8, PMA and HMGB1. Heparin, Low-Molecular-Weight 20-25 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 28958187-9 2017 At 6 h, n-Zn, b-Zn and n-Ag induced various immunity related genes associating to pattern recognition (including toll-like receptor), macrophage maturation, inflammatory response (TNF and IL-1beta), chemotaxis (CXCL8) and leucocyte migration (CXCL2-3 and CXCL14). n-zn 8-12 C-X-C motif chemokine ligand 8 Homo sapiens 211-216 28958187-9 2017 At 6 h, n-Zn, b-Zn and n-Ag induced various immunity related genes associating to pattern recognition (including toll-like receptor), macrophage maturation, inflammatory response (TNF and IL-1beta), chemotaxis (CXCL8) and leucocyte migration (CXCL2-3 and CXCL14). b-zn 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 211-216 28958187-9 2017 At 6 h, n-Zn, b-Zn and n-Ag induced various immunity related genes associating to pattern recognition (including toll-like receptor), macrophage maturation, inflammatory response (TNF and IL-1beta), chemotaxis (CXCL8) and leucocyte migration (CXCL2-3 and CXCL14). Acetylglucosamine 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 211-216 28878857-0 2017 Unusual Soft Tissue Uptake of F-18 Sodium Fluoride in Three Patients Undergoing F-18 NaF PET/CT Bone Scans for Prostate Cancer. Fluorine-18 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 28878857-0 2017 Unusual Soft Tissue Uptake of F-18 Sodium Fluoride in Three Patients Undergoing F-18 NaF PET/CT Bone Scans for Prostate Cancer. Sodium Fluoride 35-50 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 28723715-1 2017 BACKGROUND: Fluorine-18-sodium fluoride (F-NaF) PET/CT is an important tool for detecting and evaluating metastatic bone cancer. fluorine-18-sodium fluoride 12-39 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 28734155-6 2017 The mTOR inhibitor rapamycin (100nM) could attenuate the elevated expression of TF and IL-8. Sirolimus 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 28459633-6 2017 DOX would add up stimulation of CMPK1 by DTT and overcome inhibition of CMPK1 by NaF, EDTA. Doxorubicin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 28860481-8 2017 In conclusion, Siglec-9 was complementarily increased to induce a negative feedback loop to limit neutrophil activation in COPD, sSiglce-9 enhanced neutrophil ROS and chemotaxis toward IL-8 likely via competitively inhibiting ligands binding to Siglec-9. ssiglce-9 129-138 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 28836948-3 2017 Previous studies have shown that IL-8 expression is induced by pneumococcal virulence factors (e.g. pneumolysin, peptidoglycan-polysaccharides, pneumococcal surface protein A (PspA) etc. peptidoglycan-polysaccharides 113-142 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 28284032-3 2017 Recently, Greiner introduced the Vacuette FC-Mix NaF-EDTA-citrate tube, currently the only NaF-citrate tube without volume-disturbing liquid additions available on the European market. edta citrate 54-66 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 28711657-5 2017 Kaempferol decreased the production and mRNA expression of pro-inflammatory cytokines, in this case thymic stromal lymphopoietin (TSLP), IL-1beta, tumor necrosis factor (TNF)-alpha, and IL-8. kaempferol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 28711657-7 2017 Kaempferol also ameliorated the lipopolysaccharide-induced production of the inflammatory mediators TSLP, IL-1beta, TNF-alpha, IL-8, and nitric oxide of macrophage-like cells differentiated by IL-32. kaempferol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 28835236-7 2017 Interleukin-8 (IL-8) production by undifferentiated and differentiated Caco-2 cells following exposure to CuO NMs and CuSO4 was determined using an ELISA. cuo nms 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 28741944-2 2017 To analyze how UGGT recognizes non-native glycoproteins, we chemically synthesized site-specifically 15N-labeled interleukin 8 (IL-8) C-terminal (34-72) glycopeptides bearing a Man9GlcNAc2 (M9) oligosaccharide. 15n 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 28835236-7 2017 Interleukin-8 (IL-8) production by undifferentiated and differentiated Caco-2 cells following exposure to CuO NMs and CuSO4 was determined using an ELISA. cuo nms 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 28741944-2 2017 To analyze how UGGT recognizes non-native glycoproteins, we chemically synthesized site-specifically 15N-labeled interleukin 8 (IL-8) C-terminal (34-72) glycopeptides bearing a Man9GlcNAc2 (M9) oligosaccharide. 15n 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 28741944-2 2017 To analyze how UGGT recognizes non-native glycoproteins, we chemically synthesized site-specifically 15N-labeled interleukin 8 (IL-8) C-terminal (34-72) glycopeptides bearing a Man9GlcNAc2 (M9) oligosaccharide. Glycopeptides 153-166 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 28835236-15 2017 CONCLUSIONS: CuO NMs and CuSO4 stimulated IL-8 production by Caco-2 cells, decreased barrier integrity and thereby increased the Papp and translocation of Cu. Copper Sulfate 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 28741944-2 2017 To analyze how UGGT recognizes non-native glycoproteins, we chemically synthesized site-specifically 15N-labeled interleukin 8 (IL-8) C-terminal (34-72) glycopeptides bearing a Man9GlcNAc2 (M9) oligosaccharide. Glycopeptides 153-166 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 28835236-15 2017 CONCLUSIONS: CuO NMs and CuSO4 stimulated IL-8 production by Caco-2 cells, decreased barrier integrity and thereby increased the Papp and translocation of Cu. Copper 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 28624457-8 2017 The enhanced release of interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha) by the THP-1 macrophages suggested that the needle-shaped CaCO3 particles trigger a pro-inflammatory response. Calcium Carbonate 147-152 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 28643827-7 2017 We also studied the effect of sulfated alginate on the ability of IL-1beta to stimulate inflammatory genes in human chondrocytes and found decreased expression of the pro-inflammatory markers IL-6 and CXCL8, which inversely correlated with the sulfation degree. Alginates 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 201-206 28829835-5 2017 We furthermore show that vemurafenib and trametinib abrogated the activity of ERK1/2, arrested cells in G0/G1 cell cycle phase, triggered apoptosis, induced changes in the expression of CXCL8, CCND1 and CTGF and the frequency of Ki-67high and CD271high cells. Vemurafenib 25-36 C-X-C motif chemokine ligand 8 Homo sapiens 186-191 28829835-5 2017 We furthermore show that vemurafenib and trametinib abrogated the activity of ERK1/2, arrested cells in G0/G1 cell cycle phase, triggered apoptosis, induced changes in the expression of CXCL8, CCND1 and CTGF and the frequency of Ki-67high and CD271high cells. trametinib 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 186-191 28624457-8 2017 The enhanced release of interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha) by the THP-1 macrophages suggested that the needle-shaped CaCO3 particles trigger a pro-inflammatory response. Calcium Carbonate 147-152 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 28532672-1 2017 In this study, we found that catechins found in green tea (EGCG, EGC, and EC) differentially interfere with the IL-1beta signaling pathway which regulates the expression of pro-inflammatory mediators (IL-6 and IL-8) and Cox-2 in primary human rheumatoid arthritis synovial fibroblasts (RASFs). Catechin 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 28819180-5 2017 In NP cells, thrombin caused an increase in phosphorylation of the EGFR at the Tyr1068, and treatment with the pharmacological EGFR inhibitor, AG1473 effectively blocked thrombin-enhanced CXCL8 production. ag1473 143-149 C-X-C motif chemokine ligand 8 Homo sapiens 188-193 28532672-1 2017 In this study, we found that catechins found in green tea (EGCG, EGC, and EC) differentially interfere with the IL-1beta signaling pathway which regulates the expression of pro-inflammatory mediators (IL-6 and IL-8) and Cox-2 in primary human rheumatoid arthritis synovial fibroblasts (RASFs). epigallocatechin gallate 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 28532672-1 2017 In this study, we found that catechins found in green tea (EGCG, EGC, and EC) differentially interfere with the IL-1beta signaling pathway which regulates the expression of pro-inflammatory mediators (IL-6 and IL-8) and Cox-2 in primary human rheumatoid arthritis synovial fibroblasts (RASFs). gallocatechol 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 28532672-1 2017 In this study, we found that catechins found in green tea (EGCG, EGC, and EC) differentially interfere with the IL-1beta signaling pathway which regulates the expression of pro-inflammatory mediators (IL-6 and IL-8) and Cox-2 in primary human rheumatoid arthritis synovial fibroblasts (RASFs). ec 74-76 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 28532672-2 2017 EGCG and EGC inhibited IL-6, IL-8, and MMP-2 production and selectively inhibited Cox-2 expression. epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 28532672-2 2017 EGCG and EGC inhibited IL-6, IL-8, and MMP-2 production and selectively inhibited Cox-2 expression. gallocatechol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 28535933-11 2017 Additional ex vivo studies confirmed reduced induction of IL-6 (P = 0.017) and CXCL8/IL-8 (P = 0.005) with azithromycin. Azithromycin 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 28811543-0 2017 4-(E)-{(p-tolylimino)-methylbenzene-1,2-diol} (TIMBD) suppresses HIV1-gp120 mediated production of IL6 and IL8 but not CCL5. 4-(E)-((p-tolylimino)-methylbenzene-1,2-diol) 0-44 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 28328096-7 2017 Tri-DAP further increased IL-8 secretion from DSCs via JNK pathway and facilitated both MMP-2 production and trophoblast invasion compared with control. L-Ala-gamma-D-Glu-meso-diaminopimelic acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 28535933-11 2017 Additional ex vivo studies confirmed reduced induction of IL-6 (P = 0.017) and CXCL8/IL-8 (P = 0.005) with azithromycin. Azithromycin 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 28369741-6 2017 Baricitinib decreased the rate of chemotaxis towards interleukin (IL)-8, but not f-Met-Leu-Phe (fMLP) in RA neutrophils. baricitinib 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 53-71 28528743-1 2017 BACKGROUND AND AIMS: We aimed at evaluating the relation of 18F-sodium fluoride (18F-NaF) uptake on positron emission tomography (PET) to coronary atherosclerosis detected and assessed by computed tomography (CT). 18f-sodium fluoride 60-79 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 28528743-4 2017 Focal 18F-NaF uptake of each lesion was quantified using maximum tissue-to-background ratio (TBRmax). tbrmax 93-99 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 28554732-6 2017 However, atorvastatin treatment resulted in an improved St. Georges Respiratory Questionnaire (-5.62 points; P = .016) and reduced serum levels of CXCL8 (P = .04), tumor necrosis factor (P = .01), and intercellular adhesion molecule 1 (P = .04). Atorvastatin 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 147-152 28585102-7 2017 PGE2 has been shown to stimulate interleukin-8, an inflammatory cytokine that promotes the influx of neutrophils and induces remodeling of the cervical extracellular matrix, and to induce functional progesterone withdrawal. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 28371087-9 2017 Gene expressions of inflammatory markers IL-8 and MCP1 were reduced after clopidogrel treatment (P<.05); however, only MCP-1 remained reduced at protein level. Clopidogrel 74-85 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 28639412-4 2017 MATERIALS AND METHODS: The expression pattern of IL-8, TIMP-1, AP-1 transcription factor-Fra2 and ROS induction in peripheral blood monocytes following DZNep (histone methyltransferase inhibitor) and TLR8 agonist stimulation was investigated. 3-deazaneplanocin 152-157 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 28646302-9 2017 Interleukin (IL)-1beta, IL-6, IL-8 and IL-10 levels in the serum all increased POST-1h (P > 0.05) but returned to pre-exercise levels POST-1d. Hydrogen 84-86 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 28485095-9 2017 CONCLUSIONS: Overall, taking myo-inositol, compared with metformin, for 12 weeks in patients with PCOS with hyperinsulinism and normoinsulinism had beneficial effects on total testosterone, mFG scores, serum hs-CRP levels and gene expression of IL-1, but did not affect other hormonal profiles, NO levels or gene expression of IL-8 and TNF-alpha. Inositol 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 327-331 28349280-12 2017 PET/CT using 18F-NaF may be able to predict calcium score progression which is known to be the major characteristic of atherosclerosis. Calcium 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 27295033-8 2017 RESULTS: In comparison with PGOS, FOS and inulin, VGOS showed the most pronounced protective effect on the DON-induced impairment of the monolayer integrity, acceleration of the tight junction reassembly and the subsequent CXCL8 release. deoxynivalenol 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 223-228 28853522-11 2017 The addition of vitamin D significantly down-regulated IL6 and IL8 secretion and up-regulated ADAMST13 expression. Vitamin D 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 28349280-6 2017 We then evaluated the relationship between 18F-NaF uptake (using the maximum target-to-background ratio, TBRmax, and the maximum blood-subtracted 18F-NaF activity, bsNaFmax, which was obtained by subtracting the SUVmax of each calcified plaque lesion and NaF-avid site from the SUVmean in the right atrium blood pool) and the change in calcified plaque volume and characteristics obtained after 1 year. Fluorine-18 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 28349280-8 2017 18F-NaF uptake showed very weak correlations with CTmax, CTmean, CVS, CVS after 1 year, AU and AU after 1 year on both baseline and follow-up PET/CT scans for each site. ctmax 50-55 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 28349280-8 2017 18F-NaF uptake showed very weak correlations with CTmax, CTmean, CVS, CVS after 1 year, AU and AU after 1 year on both baseline and follow-up PET/CT scans for each site. ctmean 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 28349280-8 2017 18F-NaF uptake showed very weak correlations with CTmax, CTmean, CVS, CVS after 1 year, AU and AU after 1 year on both baseline and follow-up PET/CT scans for each site. Gold 88-90 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 28349280-8 2017 18F-NaF uptake showed very weak correlations with CTmax, CTmean, CVS, CVS after 1 year, AU and AU after 1 year on both baseline and follow-up PET/CT scans for each site. Gold 95-97 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 28349280-11 2017 CONCLUSION: 18F-NaF uptake has a strong correlation with calcium score progression which was a predictor of future cardiovascular disease risk. Calcium 57-64 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 28969290-3 2017 AIM: The aim of this study was to assess and compare the efficacy of iontophoresis with 0.33% Sodium Fluoride (NaF) gel and diode laser alone in dentinal tubule occlusion. Sodium Fluoride 94-109 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 28577438-5 2017 The effects of SchB on TNF-alpha and IL-8 production were detected by ELISA. schizandrin B 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 28577438-6 2017 The results showed that SchB strongly suppressed the production of TNF-alpha and IL-8 in HUVECs stimulated with LPS. schizandrin B 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 27925206-5 2017 Consistent with this mechanism, GSH depletion and hypoxia also increased ASC secretion of VEGF, IL-8, leptin, Angiopoitein-2, and PDGF-BB. Glutathione 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 28600799-5 2017 We found that PDMCs significantly reduced cardiomyocyte apoptosis and ROS production through the paracrine factors GRO-alpha, HGF and IL-8. pdmcs 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 28577438-10 2017 And the inhibition of TNF-alpha and IL-8 production by SchB was blocked by transfection with Nrf2 siRNA. schizandrin B 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 28371277-7 2017 The miR-138 mimic and LY294002 groups showed decreased concentrations of TNF-alpha, IL-6, IL-8 and NO and reduced activities of LDH and eNOS, while opposite trends were observed in the miR-138 inhibitor group. mir-138 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28371277-7 2017 The miR-138 mimic and LY294002 groups showed decreased concentrations of TNF-alpha, IL-6, IL-8 and NO and reduced activities of LDH and eNOS, while opposite trends were observed in the miR-138 inhibitor group. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28932561-8 2017 The concentrations of tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-2R, IL-6, IL-8 and IL-10 in plasma on the first postoperative day significantly increased in the GAL group than in the non-GAL group (P<0.05). Galactose 177-180 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28671329-8 2017 Moreover, OFE (1 to 100 mug/mL) showed a potent, dose-dependent inhibitory effect on H2 O2 -induced IL-8 secretion in WiDr cells. Hydrogen Peroxide 85-90 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 28671329-10 2017 Of these compounds, 5 phenolic compounds-verbascoside, phillygenin, tyrosol, methyl 4-hydroxycinnamate, and eutigoside A-reduced IL-8 secretion at 10 mug/mL treatment concentrations. phenolic 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 28671329-10 2017 Of these compounds, 5 phenolic compounds-verbascoside, phillygenin, tyrosol, methyl 4-hydroxycinnamate, and eutigoside A-reduced IL-8 secretion at 10 mug/mL treatment concentrations. acteoside 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 28671329-10 2017 Of these compounds, 5 phenolic compounds-verbascoside, phillygenin, tyrosol, methyl 4-hydroxycinnamate, and eutigoside A-reduced IL-8 secretion at 10 mug/mL treatment concentrations. phillygenin 55-66 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 28671329-10 2017 Of these compounds, 5 phenolic compounds-verbascoside, phillygenin, tyrosol, methyl 4-hydroxycinnamate, and eutigoside A-reduced IL-8 secretion at 10 mug/mL treatment concentrations. 4-hydroxyphenylethanol 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 28671329-10 2017 Of these compounds, 5 phenolic compounds-verbascoside, phillygenin, tyrosol, methyl 4-hydroxycinnamate, and eutigoside A-reduced IL-8 secretion at 10 mug/mL treatment concentrations. protocatechuic acid methyl ester 77-102 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 28671329-10 2017 Of these compounds, 5 phenolic compounds-verbascoside, phillygenin, tyrosol, methyl 4-hydroxycinnamate, and eutigoside A-reduced IL-8 secretion at 10 mug/mL treatment concentrations. eutigoside A 108-120 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 28611093-4 2017 Danirixin is a competitive antagonist against CXCL8 in Ca2+-mobilization assays, with a KB (the concentration of antagonist that binds 50% of the receptor population) of 6.5 nM and antagonist potency (pA2) of 8.44, and is fully reversible in washout experiments over 180 minutes. danirixin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 46-51 28247536-7 2017 The interaction between the telomeric repeat-containing RNA (TERRA) and PARP-1 stimulates the SASP, which was attenuated by 67.9% (illustrated by the case of IL8) by treatment with melatonin. Melatonin 181-190 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 28411127-0 2017 Preventing false-negatives in the in vitro skin sensitization testing of acid anhydrides using interleukin-8 release assays. acid anhydrides 73-88 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 28586015-4 2017 The results indicated that Met, UC-II, CS, MSM and AO slightly or moderately suppressed the IL-1beta-stimulated IL-8 production by human synovial MH7A cells. Chondroitin Sulfates 39-41 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 28586015-5 2017 The same compounds further decreased the IL-8 level lowered by GlcN. Glucosamine 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 28867672-8 2017 IL-8 secretion increased with flavor and nicotine, while TNFalpha, IL-1beta, IL-6, MIP-1alpha, MIP-1beta, and MCP-1 decreased after exposure to most flavors and nicotine. Nicotine 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 28414142-9 2017 However, when we examine the effect of doxofylline on secretion of the interleukin 8 from ASM cells stimulated by tumour necrosis factor (an in vitro surrogate measure of inflammation), there was no repression of inflammation. doxofylline 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 28411127-6 2017 Additionally, treatment of THP-1 cells with PAH and phthalic acid using LP dispersion medium for 5min resulted in a 32-fold increase in IL-8 release for PAH as compared with that in the vehicle control. phthalic anhydride 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 28411127-6 2017 Additionally, treatment of THP-1 cells with PAH and phthalic acid using LP dispersion medium for 5min resulted in a 32-fold increase in IL-8 release for PAH as compared with that in the vehicle control. phthalic acid 52-65 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 28411127-6 2017 Additionally, treatment of THP-1 cells with PAH and phthalic acid using LP dispersion medium for 5min resulted in a 32-fold increase in IL-8 release for PAH as compared with that in the vehicle control. Mineral Oil 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 28411127-6 2017 Additionally, treatment of THP-1 cells with PAH and phthalic acid using LP dispersion medium for 5min resulted in a 32-fold increase in IL-8 release for PAH as compared with that in the vehicle control. phthalic anhydride 153-156 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 28411127-8 2017 Similarly, using LP dispersion medium, trimellitic anhydride significantly increased IL-8 release was observed. Mineral Oil 17-19 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 28773202-6 2017 Furthermore, the bio-composites that included bio-lignin at 0.1% have been able to modulate the expression of pro-inflammatory cytokines (Tumor Necrosis Factor-alpha, IL-1alpha, and IL8), lipopolysaccharide (LPS)-induced, and matrix metalloproteinases (MMPs) and human beta-defensin 2 (HBD-2) expression in HaCat cells, suggesting an anti-inflammatory and immunomodulatory role. Lignin 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 28756770-14 2017 Additionally, elevated RNF183 expression partly reduced the inhibitory effect of trametinib on IL-8 expression. trametinib 81-91 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 28756770-16 2017 CONCLUSION: The RNF183-IL-8 axis is responsible for the resistance of CRC cells to the MEK1/2 inhibitor trametinib and may serve as a candidate target for combined therapy for CRC. trametinib 104-114 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 28749642-0 2017 Combination Therapy with Low Copper Diet, Penicillamine and Gamma Knife Radiosurgery Reduces VEGF and IL-8 In Patients with Recurrent Glioblastoma Purpose: Vascular Endothelial Growth Factor (VEGF) and interleukin-8 (IL-8) appear important in tumor growth. Copper 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 28749642-0 2017 Combination Therapy with Low Copper Diet, Penicillamine and Gamma Knife Radiosurgery Reduces VEGF and IL-8 In Patients with Recurrent Glioblastoma Purpose: Vascular Endothelial Growth Factor (VEGF) and interleukin-8 (IL-8) appear important in tumor growth. Penicillamine 42-55 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 28749642-1 2017 Inthis study, we have investigated the effect of copper reduction along with gamma knife radiosurgery on IL-8 and VEGFin patients with recurrent glioblastoma multiforme (GBM). Copper 49-55 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 28724795-8 2017 SAA and aliquots of LXA4loSAAhi BAL fluid induced IL-8 production by lung epithelial cells expressing ALX receptors, which was inhibited by coincubation with 15-epi-LXA4. lipoxin A4 158-169 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 28947965-11 2017 Significantly, inhibition of the IL-8 signaling pathway by reparixin, an inhibitor of the IL-8 receptor, CXCR1/2, reduced MDA-MB-231 tumor growth and metastasis. reparixin 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 28947965-11 2017 Significantly, inhibition of the IL-8 signaling pathway by reparixin, an inhibitor of the IL-8 receptor, CXCR1/2, reduced MDA-MB-231 tumor growth and metastasis. reparixin 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28703802-5 2017 It can also be diminished by IL8-neutralizing antibody or blockade of IL8 receptors CXCR1/2 with reparixin. reparixin 97-106 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 29798256-5 2017 The levels of IL-1beta, IL-8 and TNF-alpha in saliva were lower on the third day and fifth day (P< 0.05).Conclusion:Applying Cetylpyridinium Chloride Buccal Tablets during perioperative period can effectively relieve postoperative pharyngeal pain and inflammatory response in patients with OSAHS. cetylpyridinium chloride buccal 128-159 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 28288142-7 2017 Unbiased large-scale metabolomic analysis and transcriptome-wide mRNA expression profiling identified reduced levels of several metabolites of the amino sugar and nucleotide sugar metabolic pathways, including sialic acid N-acetylneuraminic acid (Neu5Ac), and downregulation of pro-oncogenic cytokines interleukin-6 and 8 (IL-6 and IL-8) as unexpected outcomes of SHMT1 loss. Amino Sugars 147-158 C-X-C motif chemokine ligand 8 Homo sapiens 332-336 28288142-7 2017 Unbiased large-scale metabolomic analysis and transcriptome-wide mRNA expression profiling identified reduced levels of several metabolites of the amino sugar and nucleotide sugar metabolic pathways, including sialic acid N-acetylneuraminic acid (Neu5Ac), and downregulation of pro-oncogenic cytokines interleukin-6 and 8 (IL-6 and IL-8) as unexpected outcomes of SHMT1 loss. N-Acetylneuraminic Acid 210-221 C-X-C motif chemokine ligand 8 Homo sapiens 332-336 28288142-9 2017 Supplementation of culture medium with Neu5Ac stimulated expression of IL-6 and IL-8 and rescued the tumor growth and migratory phenotypes of ovarian cancer cells expressing SHMT1 shRNAs. N-Acetylneuraminic Acid 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30090537-5 2017 The mRNA levels of IL-6, IL-8, TNF-alpha and IL-1beta were upregulated by SiO2 NP or cold exposure, and more so in the combined group. sio2 np 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 28347830-7 2017 RESULTS: In human keratinocytic HaCaT cells, PS extract inhibited the production of IL-8, and TARC, which had been increased by TNF-alpha and IFN-gamma. ps 45-47 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 30090537-6 2017 The expressions of the proinflammatory cytokine genes IL-6, IL-8, TNF-alpha and IL-1beta increased highly significantly (P < 0.01) in the SiO2 NP alone group and the combined group, compared with the control. sio2 np 141-148 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 28369685-5 2017 Effects of isorhapontigenin and resveratrol on the release of IL-6 and chemokine (C-X-C motif) ligand 8 (CXCL8), and the activation of NF-kappaB, activator protein-1 (AP-1), MAPKs and PI3K/Akt/FoxO3A pathways were determined and compared with those of dexamethasone. Resveratrol 32-43 C-X-C motif chemokine ligand 8 Homo sapiens 105-110 28643288-6 2017 H2O2 treatment increased both the protein and mRNA levels of IL-1beta, IL-8, and TNF-alpha, as well as those of SAPK/JNK. Hydrogen Peroxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 28643288-8 2017 In summary, the PAR2 antagonist peptide, FSLLRY-NH2, reduces the level of the pro-inflammatory genes IL-8, IL-1beta, and TNF-alpha induced by H2O2, through the SAPK/JNK pathways in HepG2 cells. Hydrogen Peroxide 142-146 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 28229451-5 2017 RESULTS: Honokiol at 10 mum reduced IL-1alpha production by 3.4 folds (P < 0.05) and at 10 and 20 mum reduced IL-8 by 23.9% and 53.1% (P < 0.001), respectively, in HaCat keratinocytes. honokiol 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 28176455-12 2017 Additionally, WZ4003 and SB203580 could suppress the APN-induced overexpression of CXCL1 and CXCL8. WZ4003 14-20 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 28176455-12 2017 Additionally, WZ4003 and SB203580 could suppress the APN-induced overexpression of CXCL1 and CXCL8. SB 203580 25-33 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 28220523-9 2017 Palmitic acid also up-regulated interleukin-8 (a key chemokine for human neutrophil recruitment) expression in human hepatocytes, which was attenuated and enhanced by cotreatment with a PPARgamma agonist and antagonist, respectively. Palmitic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 28534957-6 2017 Pretreatment with GSP before LPS treatment significantly suppressed the mRNA expression of pro-inflammatory cytokines such as IL-1beta, IL-6 and IL-8. Grape Seed Proanthocyanidins 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 28671563-5 2017 The results showed that I3C and DIM pretreatment, at higher concentrations of 50 and 10 muM, respectively, significantly increased PMA/ionomycin-induced interleukin-2 (IL-2), interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha) production, measured by real time polymerase chain reaction (RT-PCR) and enzyme linked immunosorbent assay (ELISA). Ionomycin 135-144 C-X-C motif chemokine ligand 8 Homo sapiens 175-188 28671563-5 2017 The results showed that I3C and DIM pretreatment, at higher concentrations of 50 and 10 muM, respectively, significantly increased PMA/ionomycin-induced interleukin-2 (IL-2), interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha) production, measured by real time polymerase chain reaction (RT-PCR) and enzyme linked immunosorbent assay (ELISA). Ionomycin 135-144 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 28099236-9 2017 After 3 days, perfluorohexane treatment significantly (P < .05) increased lung dynamic compliance, and reduced alveolar-arterial oxygen gradient, Acute Physiology and Chronic Health Evaluation II score, percentage of neutrophils, and levels of interleukin-6, interleukin-8, and tumor necrosis factor alpha in bronchoalveolar lavage fluid; there was no significant change in the control group before and after treatment. perflexane 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 262-275 29285030-10 2017 Resveratrol significantly inhibited LPS-induced IL-6 and IL-8 secretion by HGFs, but silymarin did not show such a significant effect. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 28369685-8 2017 KEY RESULTS: Isorhapontigenin concentration-dependently inhibited IL-6 and CXCL8 release, with IC50 values at least twofold lower than those of resveratrol. isorhapontigenin 13-29 C-X-C motif chemokine ligand 8 Homo sapiens 75-80 28643000-0 2017 Interaction of the interleukin 8 protein with a sodium dodecyl sulfate micelle: A computer simulation study. Sodium Dodecyl Sulfate 48-70 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 27977904-0 2017 Adenosine triphosphate induces P2Y2 activation and interleukin-8 release in human esophageal epithelial cells. Adenosine Triphosphate 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 27977904-3 2017 This study characterized and identified human esophageal epithelial P2 receptors that are responsible for ATP-mediated release of IL-8 by using a human esophageal stratified squamous epithelial model. Adenosine Triphosphate 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 27977904-8 2017 RESULTS: Adenosine triphosphate-gamma-S induced IL-8 release through the P2Y2 receptor. adenosine triphosphate-gamma-s 9-39 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 27977904-9 2017 A P2Y2 receptor antagonist but not a P2X3 receptor antagonist or a P2Y1 receptor antagonist blocked ATP-gamma-S-mediated IL-8 release. adenosine 5'-O-(3-thiotriphosphate) 100-111 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 27977904-12 2017 Inhibition of extracellular signal-regulated kinase but not of protein kinase C blocked the ATP-mediated release of IL-8. Adenosine Triphosphate 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 27977904-15 2017 ATP-induced IL-8 release maybe involved in the pathogenesis of refractory gastroesophageal reflux disease. Adenosine Triphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 28643000-2 2017 Simulations for an SDS micelle with an IL8 protein show that both aggregates, which were initially separated, eventually approach each other to form a single complex. Sodium Dodecyl Sulfate 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 28643000-6 2017 Graphical Abstract Attachment of the interleukin 8 protein with a sodium dodecyl sulfate (SDS) micelle is given by the charged positive amino acids as indicated by the interaction of those amino acids with the SDS headgroups. Sodium Dodecyl Sulfate 66-88 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 28643000-6 2017 Graphical Abstract Attachment of the interleukin 8 protein with a sodium dodecyl sulfate (SDS) micelle is given by the charged positive amino acids as indicated by the interaction of those amino acids with the SDS headgroups. Sodium Dodecyl Sulfate 90-93 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 28643000-6 2017 Graphical Abstract Attachment of the interleukin 8 protein with a sodium dodecyl sulfate (SDS) micelle is given by the charged positive amino acids as indicated by the interaction of those amino acids with the SDS headgroups. Sodium Dodecyl Sulfate 210-213 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 28412309-3 2017 In analogy to endogenous androgens, nandrolone induced a dose-related increase in RACK1 transcriptional activity and protein expression, resulting in increased LPS-induced IL-8 and TNF-alpha production and proliferation in THP-1 cells. Nandrolone 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 28667247-10 2017 Compared with the other groups, the combination of Astragaloside and Baicalin more efficiently reduced IL-1beta, IL-8, and TNF-alpha levels in the LPS-induced MSCs model, and ERK inhibitor was capable of recovering the inflammatory effect. astragaloside 51-64 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 28667247-10 2017 Compared with the other groups, the combination of Astragaloside and Baicalin more efficiently reduced IL-1beta, IL-8, and TNF-alpha levels in the LPS-induced MSCs model, and ERK inhibitor was capable of recovering the inflammatory effect. baicalin 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 28356331-9 2017 Quiescent human prostate stroma exposed to genotoxic agents (e.g., mitoxantrone) in vivo resulted in significant upregulation (2.7- to 5.7-fold; P <= 0.01) of growth factors and cytokines including IL1beta, MMP3, IL6, and IL8. Mitoxantrone 67-79 C-X-C motif chemokine ligand 8 Homo sapiens 225-228 28670183-1 2017 We evaluated the association between serum prostate specific antigen (PSA) level and kinetics to predict 18F-sodium fluoride positron emission tomography-computed tomography (18F-NaF PET-CT) positivity for first bone metastases in men with biochemical recurrence after radical prostatectomy. Sodium Fluoride 109-124 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 28442557-5 2017 Incubation of cells in an HP (3.3 mM) medium caused an increased expression of the pro-inflammatory mediators intercellular adhesion molecule 1 (ICAM-1), interleukins (ILs) IL-1beta, IL-6, IL-8 and tumour necrosis factor alpha (TNF-alpha) (not corroborated at the protein levels for ICAM-1), as well as an increase in reactive oxygen/nitrogen species (ROS/RNS) production. Hematoporphyrins 26-28 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 28392494-2 2017 First, the preparation of nanoparticles in the presence of sodium fluoride (NaF) as the active ingredient by ionic gelation was investigated followed by an evaluation of their drug entrapment and release properties. Sodium Fluoride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 28392494-5 2017 A steady increase in the fluoride release was observed for chitosan nanoparticles prepared in 0.2% NaF both in pH5 and 7 until it reached a maximum at time point 4h and maintained at this level for at least 24h. Fluorides 25-33 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 28392494-6 2017 Similar profiles were observed for formulations prepared in 0.4% NaF; however the fluoride was released at a higher level at pH5. Fluorides 82-90 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 28527783-9 2017 In addition, TIM-38 inhibited UDP-induced interleukin-8 release in a dose-dependent manner without affecting releases caused by other stimulus such as interleukin-1beta or tumour necrosis factor-alpha. 3-nitro-2-(trifluoromethyl)-2H-chromene 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 28527783-9 2017 In addition, TIM-38 inhibited UDP-induced interleukin-8 release in a dose-dependent manner without affecting releases caused by other stimulus such as interleukin-1beta or tumour necrosis factor-alpha. Uridine Diphosphate 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 28808406-9 2017 RESULTS: Peimine inhibited the production of pro-inflammatory cytokines, such as IL-6, IL-8, and TNF-alpha. verticine 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 28808406-13 2017 SUMMARY: Peimine inhibited the production of pro-inflammatory cytokines, such as IL-6, IL-8, and TNF-alphaPeimine reduced MAPKs phosphorylation and the nuclear NF-kappaB expression in PMACI-induced HMC-1Peimine decreased PCA reactions in ratsPeimine has anti-allergic effect through regulation of pro-inflammatory mechanism on mast cell. verticine 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 28665978-9 2017 Our results demonstrated testosterone not only suppressed the invasion and colonization of UPEC, but also inhibited the expression of pro-inflammatory IL-1beta, IL-6 and IL-8 cytokines expression induced by UPEC in a dose-dependent manner. Testosterone 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 28730070-1 2017 AIM: To study the effects of curcumin on the secretion of interleukin (IL)-6 and IL-8 by corneal limbus epithelial cells. Curcumin 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 28730070-8 2017 Various signal pathway inhibitors, including SP600125 (JNK inhibitor), SB203580 (p38 MAPK inhibitor) and BAY11-7082 (NF-kappaB inhibitor) significantly decreased the UVB-induced secretion of IL-6 and IL-8 secretion (P<0.05). 3-(4-methylphenylsulfonyl)-2-propenenitrile 105-115 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 28730070-9 2017 Curcumin at 5-20 micromol/L significantly inhibited UVB-induced secretion of IL-6 and IL-8 by limbus epithelial cells in a dose-dependent manner; while curcumin alone did not affect the secretion of IL-6 and IL-8. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 28730070-9 2017 Curcumin at 5-20 micromol/L significantly inhibited UVB-induced secretion of IL-6 and IL-8 by limbus epithelial cells in a dose-dependent manner; while curcumin alone did not affect the secretion of IL-6 and IL-8. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 28730070-10 2017 The upregulation of NF-kappaB and MAPK pathways induced by UVB treatment was significantly inhibited by curcumin, suggesting that NF-kappaB and MAPK pathways are involved in the inhibitory effect of curcumin on UVB-induced production of IL-6 and IL-8. Curcumin 104-112 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 28730070-10 2017 The upregulation of NF-kappaB and MAPK pathways induced by UVB treatment was significantly inhibited by curcumin, suggesting that NF-kappaB and MAPK pathways are involved in the inhibitory effect of curcumin on UVB-induced production of IL-6 and IL-8. Curcumin 199-207 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 28418782-10 2017 Increased levels of p-Akt and decreased levels of FOXO3a protein expression suggested that reactive oxygen species played a role in the initiation and maintenance of senescence in IL-8-silenced PMSCs. Reactive Oxygen Species 91-114 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 28606092-6 2017 In addition, we found an increase in the cytokine secretion of IL-6 and chemokine IL-8 in FFA-treated HC in comparison to the untreated HC. Fatty Acids, Nonesterified 90-93 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 28614381-0 2017 The cytotoxic effect of TiF4 and NaF on fibroblasts is influenced by the experimental model, fluoride concentration and exposure time. Fluorides 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 28600524-9 2017 In addition, cotinine and nicotine-cotinine mixture suppressed VEGF and IL-8 expression and upregulated TIMP-2 expression. Cotinine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 28664168-1 2017 This article contains the data showing illustrative examples of plaque classification on coronary computed tomography angiography (CCTA) and measurement of 18F-sodium fluoride (18F-NaF) uptake in coronary atherosclerotic lesions on positron emission tomography (PET). 18f-sodium fluoride 156-175 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 28600524-9 2017 In addition, cotinine and nicotine-cotinine mixture suppressed VEGF and IL-8 expression and upregulated TIMP-2 expression. Nicotine 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 28600524-9 2017 In addition, cotinine and nicotine-cotinine mixture suppressed VEGF and IL-8 expression and upregulated TIMP-2 expression. Cotinine 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 28238270-6 2017 TMZ treatment led to a decrease in IL-2 concentrations before TET, as well as it prevented the increase of IL-8 following the second TET. tet 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 28575053-8 2017 Treatment of HUVECs with U0126, an ERK1/2 signaling inhibitor, attenuated autocrine production of IL-8 induced by Mxi1-0 overexpression. U 0126 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 28238270-0 2017 Effects of trimetazidine on interleukin-2 and interleukin-8 concentrations in patients with coronary artery disease. Trimetazidine 11-24 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 28238270-7 2017 Obtained results confirmed the improvement in TET performance during TMZ treatment and they revealed a significant influence of TMZ on IL-2 and IL-8 concentrations both before and after TET. Trimetazidine 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 28238270-6 2017 TMZ treatment led to a decrease in IL-2 concentrations before TET, as well as it prevented the increase of IL-8 following the second TET. Trimetazidine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 30087790-2 2017 Early events in inflammation involve the recruitment of neutrophils to the site of injury or damage where changes in intracellular calcium can cause the activation of pro-inflammatory mediators from neutrophils including superoxide generation, degranulation and release of myeloperoxidase (MPO), productions of interleukin (IL)-8 and tumor necrosis factor alpha (TNF-alpha), and adhesion to the vascular endothelium. Calcium 131-138 C-X-C motif chemokine ligand 8 Homo sapiens 311-329 28317149-9 2017 CONCLUSION: In the PCPT finasteride arm, variation in genes involved in the immune response, including possibly IL8 and IL10 as in the placebo arm, may be associated with prostate cancer, especially higher-grade disease, but not with intraprostatic inflammation. pcpt 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 28333279-14 2017 In human foetal membranes, PIM1 inhibitors SMI-4a and AZD1208 significantly decreased the expression of pro-inflammatory cytokine interleukin-6 (IL6) and chemokines CXCL8 and CCL2 mRNA and release, prostaglandin prostaglandin F2alpha (PGF2alpha) release, adhesion molecule intercellular adhesion molecule 1 mRNA expression and release, and oxidative stress marker 8-isoprostane release after stimulation with either LPS or flagellin. AZD1208 54-61 C-X-C motif chemokine ligand 8 Homo sapiens 165-170 28317149-9 2017 CONCLUSION: In the PCPT finasteride arm, variation in genes involved in the immune response, including possibly IL8 and IL10 as in the placebo arm, may be associated with prostate cancer, especially higher-grade disease, but not with intraprostatic inflammation. Finasteride 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 29849682-4 2017 The level of serum IL-8 was compared between the glucocorticosteroid groups, receiving inhaled corticosteroids (ICs), oral corticosteroids (OCs), and intravenous corticosteroids (GCs), respectively. glucocorticosteroid 49-68 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 29849682-4 2017 The level of serum IL-8 was compared between the glucocorticosteroid groups, receiving inhaled corticosteroids (ICs), oral corticosteroids (OCs), and intravenous corticosteroids (GCs), respectively. Iron-Sulfur-Molybdenum Cluster With Interstitial Carbon 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 28214551-3 2017 The BAK effect at 10-4% or 5.10-3% on the gene expressions of interleukin-6 (IL-6), interleukin-8 (IL-8) and matrix metalloproteinase (MMP-9) was investigated using qRT-PCR in 2D and 3D p-hTMC cultures. Benzalkonium Compounds 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 28214551-3 2017 The BAK effect at 10-4% or 5.10-3% on the gene expressions of interleukin-6 (IL-6), interleukin-8 (IL-8) and matrix metalloproteinase (MMP-9) was investigated using qRT-PCR in 2D and 3D p-hTMC cultures. Benzalkonium Compounds 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 29849682-4 2017 The level of serum IL-8 was compared between the glucocorticosteroid groups, receiving inhaled corticosteroids (ICs), oral corticosteroids (OCs), and intravenous corticosteroids (GCs), respectively. L-Cysteic acid 140-143 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 28214551-5 2017 IL-6 and IL-8 gene expressions increased in presence of BAK in 2D and in 3D p-hTMC cultures. Benzalkonium Compounds 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 29849682-5 2017 Changes in the serum IL-8 level were compared between asthmatics with good and poor glucocorticosteroid responsiveness. glucocorticosteroid 84-103 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 29849682-8 2017 The area under curve (AUC) for serum IL-8 level, indicative of uncontrolled asthma, was 0.816 (95% CI, 0.7605 to 0.8721; P< 0.0001), which was greater than the AUC of fractional exhaled nitric oxide (AUC, 0.711; 95% CI, 0.6057 to 0.8153; P= .0188). Nitric Oxide 189-201 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 29849682-13 2017 The change in IL-8 level also reflects the response to glucocorticosteroids in uncontrolled asthma. glucocorticosteroids 55-75 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 28363866-9 2017 Transfection of poly(I-C) enhanced IL8 and BST2 mRNA expression and inhibited HBsAg secretion from PLC/PRF/5 cells. Poly I-C 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 28539592-7 2017 Furthermore, atorvastatin was able to block the induction of interleukins IL-6 and IL-8 triggered by pathologic stimuli relevant to AMD, such as cholesterol crystals and ox-LDL. Atorvastatin 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 28539592-7 2017 Furthermore, atorvastatin was able to block the induction of interleukins IL-6 and IL-8 triggered by pathologic stimuli relevant to AMD, such as cholesterol crystals and ox-LDL. Cholesterol 145-156 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 28169521-8 2017 AY254, but not AY77 or DF253, attenuated cytokine-induced caspase 3/8 activation, promoted scratch-wound healing, and induced IL-8 secretion, all via PAR2-ERK1/2 signaling. ay254 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 27821605-9 2017 Multivariate analyses identified IL6 and IL8 as independent predictors of OS.Conclusions: Foretinib demonstrated promising antitumor activity and good tolerability in the first-line setting in Asian advanced hepatocellular carcinoma patients. GSK 1363089 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 28396316-7 2017 Neutralization studies identified IL-6 and CXCL8 as factors secreted by EVTs that induce endothelial cell CCL14 and CXCL6 expression. evts 72-76 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 28486961-6 2017 Heparin reduced the expression of pro-inflammatory markers (TNF-alpha and IL-6) in hAM and deactivated the NF-kss pathway in hATII, diminishing the expression of IRAK1 and MyD88 and their effectors, IL-6, MCP-1 and IL-8. Heparin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 28487429-9 2017 Additional cytokine secretion screening identified molecules that induce levels of tumor necrosis factor alpha (TNF-alpha) and interleukin-8 (IL-8) comparable to the levels induced by phosphorylated hexa-acyl disaccharide (PHAD). UNII-5A35GQS15R 223-227 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 28539656-3 2017 Here, we show that Tat-induced CXCL8 production is essentially dependent on the activation of PKC delta isoform, as shown a) by the capacity of PKC delta dominant negative (DN), and Rottlerin, a selective PKC delta pharmacological inhibitor, to inhibit Tat-induced CXCL8 production and b) by the ability of the constitutively active (CAT) isoform of PKC delta to induce CXCL8 production in a HEK cell line in the absence of Tat stimulation. rottlerin 182-191 C-X-C motif chemokine ligand 8 Homo sapiens 31-36 28235736-6 2017 The receptor R is able to detect sodium salts of flouride (NaF) and acetate (NaAcO) in aqueous medium and it exhibited dramatic color change from pale yellow to red. sodium salts 33-45 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 28235736-6 2017 The receptor R is able to detect sodium salts of flouride (NaF) and acetate (NaAcO) in aqueous medium and it exhibited dramatic color change from pale yellow to red. flouride 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 28235736-6 2017 The receptor R is able to detect sodium salts of flouride (NaF) and acetate (NaAcO) in aqueous medium and it exhibited dramatic color change from pale yellow to red. naaco 77-82 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 29029391-6 2017 Down-regulation of interleukin 8 (IL-8) in a dose- and time-dependent manner was observed in ginsenoside Rg3-treated stromal cells, and over-expression or addition of IL-8 reversed the anti-senescence role of Rg3 in prostate stromal cells. Ginsenosides 93-104 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 29029391-0 2017 Ginsenoside Rg3 inhibits the senescence of prostate stromal cells through down-regulation of interleukin 8 expression. Ginsenosides 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 93-106 29029391-6 2017 Down-regulation of interleukin 8 (IL-8) in a dose- and time-dependent manner was observed in ginsenoside Rg3-treated stromal cells, and over-expression or addition of IL-8 reversed the anti-senescence role of Rg3 in prostate stromal cells. Ginsenosides 93-104 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 29029391-6 2017 Down-regulation of interleukin 8 (IL-8) in a dose- and time-dependent manner was observed in ginsenoside Rg3-treated stromal cells, and over-expression or addition of IL-8 reversed the anti-senescence role of Rg3 in prostate stromal cells. Ginsenosides 93-104 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 29029391-7 2017 Furthermore, ginsenoside Rg3 down-regulated IL-8 expression by decreasing the reactive oxygen species level in prostatic stromal cells and reducing the transcriptional activity of IL-8 promoter by damping the transcription factors C/EBP beta and p65 binding to IL-8 promoter. Ginsenosides 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 29029391-7 2017 Furthermore, ginsenoside Rg3 down-regulated IL-8 expression by decreasing the reactive oxygen species level in prostatic stromal cells and reducing the transcriptional activity of IL-8 promoter by damping the transcription factors C/EBP beta and p65 binding to IL-8 promoter. Ginsenosides 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 29029391-7 2017 Furthermore, ginsenoside Rg3 down-regulated IL-8 expression by decreasing the reactive oxygen species level in prostatic stromal cells and reducing the transcriptional activity of IL-8 promoter by damping the transcription factors C/EBP beta and p65 binding to IL-8 promoter. Ginsenosides 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 29029391-7 2017 Furthermore, ginsenoside Rg3 down-regulated IL-8 expression by decreasing the reactive oxygen species level in prostatic stromal cells and reducing the transcriptional activity of IL-8 promoter by damping the transcription factors C/EBP beta and p65 binding to IL-8 promoter. Reactive Oxygen Species 78-101 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 29029391-8 2017 Our research revealed that ginsenoside Rg3 was able to inhibit prostate stromal cell senescence by down-regulating IL-8 expression. Ginsenosides 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 28339192-8 2017 Using the optimized inverted ALI/postincubation procedure, pro-inflammatory immune responses, in terms of interleukin (IL)-8 promoter and nuclear factor kappa B (NFkappaB) activity, were observed within short time, i.e. One hour exposure to ALI-deposited CuO-NPs and 2.5 h postincubation. ali 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 106-124 28429305-4 2017 Macrolide antibiotics have demonstrated great benefit when used for their anti-inflammatory or immunomodulatory properties, which include the blockage of pro-inflammatory cytokines, such as interleukin (IL)-8 and tumor necrosis factor-alpha (TNF-alpha). macrolide antibiotics 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 190-208 28292012-4 2017 DEHP treatment also increased the expression of interleukin-6 (IL-6) and IL-8. Diethylhexyl Phthalate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 27639185-5 2017 VPA and lithium both induce significant down-regulation of group I CD1 expression and secretion of IL-6 during differentiation of human monocyte-derived immature DC, while they differ in the induction of CD83 and CD86 expression, secretion of IL-8, IL-10, and TNF-alpha. Valproic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 28101945-8 2017 And using the erlotinib as an inhibitor of EGFR, we identified the erlotinib impaired the phosphorylation of EGFR, ERK1/2, acetylation of NF-kappaB proteins and decreased IL-8. Erlotinib Hydrochloride 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 27798431-6 2017 RESULTS: We show that, in contrast to RAL, ritonavir treatment significantly increases mRNA expression levels of HO-1, IL-8, TNFalpha, CCL5, and MCP-1 in vitro in a dose-dependent manner. Ritonavir 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 27917510-9 2017 N-acetyl-l-cysteine suppressed MeHg-induced activation of IL-6 and IL-8 mRNA expression in U937 macrophages, indicating the effectiveness of N-acetyl-l-cysteine as a therapeutic drug in MeHg-induced inflammation. Acetylcysteine 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 27917510-9 2017 N-acetyl-l-cysteine suppressed MeHg-induced activation of IL-6 and IL-8 mRNA expression in U937 macrophages, indicating the effectiveness of N-acetyl-l-cysteine as a therapeutic drug in MeHg-induced inflammation. Acetylcysteine 141-160 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 28101945-8 2017 And using the erlotinib as an inhibitor of EGFR, we identified the erlotinib impaired the phosphorylation of EGFR, ERK1/2, acetylation of NF-kappaB proteins and decreased IL-8. Erlotinib Hydrochloride 67-76 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 27682001-6 2017 PFOA enhanced gene expression of several pro-inflammatory cytokines, including tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, IL-6, and IL-8 by the activation of nuclear factor (NF)-kappaB in IgE-stimulated mast cells. perfluorooctanoic acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 27639185-5 2017 VPA and lithium both induce significant down-regulation of group I CD1 expression and secretion of IL-6 during differentiation of human monocyte-derived immature DC, while they differ in the induction of CD83 and CD86 expression, secretion of IL-8, IL-10, and TNF-alpha. Lithium 8-15 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 27881328-8 2017 The alloy-exposed culture media tested contained sufficient stimulatory metal ions to induce detectable IL-8 production in THP-1 cells, except for the Ni-Cr and stainless steel exposed media. Metals 72-77 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 28532624-6 2017 METHODS: The effects of AG-related compounds on H2O2-induced changes in intracellular Ca2+ concentrations, extracellular signal-regulated kinase (ERK) activation, and CXCL8 secretion were assessed using U937 cells. Hydrogen Peroxide 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 167-172 28532624-9 2017 CONCLUSION: Our results show that AG-related compounds inhibit H2O2-induced CXCL8 secretion following ERK activation, which is mediated by TRPM2-dependent and -independent mechanisms in U937 cells. Hydrogen Peroxide 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 76-81 27881328-9 2017 Au and Pd-Cu alloys were also most effective in potentiating LPS responsiveness as measured by IL-8 production. Gold 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 27881328-9 2017 Au and Pd-Cu alloys were also most effective in potentiating LPS responsiveness as measured by IL-8 production. pd-cu 7-12 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 27624778-0 2017 ROS-dependent HMGB1 secretion upregulates IL-8 in upper airway epithelial cells under hypoxic condition. Reactive Oxygen Species 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 28288823-0 2017 Cadmium-induced IL-6 and IL-8 expression and release from astrocytes are mediated by MAPK and NF-kappaB pathways. Cadmium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 28288823-3 2017 In the peripheral system, cadmium promotes interleukin-6 (IL-6) and IL-8 production and release. Cadmium 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 28288823-12 2017 Pretreatment with U0126-an inhibitor of MEK1 and MEK2 kinases-SB203580-a p38 MAPK inhibitor-and SC-514-an IKKbeta inhibitor-suppressed cadmium-induced IL-8 expression and release. SB 203580 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 28288823-6 2017 Herein, the effects of non-toxic concentrations of cadmium on the production of IL-6 and IL-8 and the underlying mechanisms were investigated. Cadmium 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 28288823-12 2017 Pretreatment with U0126-an inhibitor of MEK1 and MEK2 kinases-SB203580-a p38 MAPK inhibitor-and SC-514-an IKKbeta inhibitor-suppressed cadmium-induced IL-8 expression and release. Cadmium 135-142 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 28288823-15 2017 In conclusion, non-toxic concentrations of cadmium can stimulate IL-6 and IL-8 release through MAPK phosphorylation and NF-kappaB activation. Cadmium 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 28288823-10 2017 IL-6 and IL-8 mRNA levels and secretion increased in dose- and time-dependent manners post cadmium exposure. Cadmium 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 28288823-16 2017 Suppressing IL-6 and IL-8 production could be novel approaches to prevent cadmium-induced angiogenesis in gliomas and inflammation in the brain. Cadmium 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 28288823-12 2017 Pretreatment with U0126-an inhibitor of MEK1 and MEK2 kinases-SB203580-a p38 MAPK inhibitor-and SC-514-an IKKbeta inhibitor-suppressed cadmium-induced IL-8 expression and release. U 0126 18-23 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 28438162-12 2017 Comparably, the in vitro experiments showed that FK866 also inhibited IL-8 production and NF-kappaB activation in human alveolar epithelial cells exposed to H/R. N-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamide 49-54 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 28496415-4 2017 We previously reported that exposure of human bronchial epithelial cells (HBECs) to non-menthol cigarette smoke extract (Non-M-CSE) triggers a cascade of inflammatory signaling leading to IL-8 induction. Menthol 88-95 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 28438134-0 2017 Poly I:C induces collective migration of HaCaT keratinocytes via IL-8. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 28438134-8 2017 Poly I:C also increased IL-8 and bFGF production, and anti-IL-8 antibodies significantly inhibited the migration caused by poly I:C. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 28438134-8 2017 Poly I:C also increased IL-8 and bFGF production, and anti-IL-8 antibodies significantly inhibited the migration caused by poly I:C. Poly I-C 123-131 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 28438134-12 2017 CONCLUSION: Our findings demonstrated that poly I:C accelerated collective HaCaT cell migration via autocrine/paracrine secretions of IL-8 and the subsequent incomplete epithelial-mesenchymal transition (EMT). Poly I-C 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 28554966-9 2017 While PiC and CDCA increased IL-8 production, LCA reduced both basal and PiC +- CDCA-induced IL-8 production. pic 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 28554966-9 2017 While PiC and CDCA increased IL-8 production, LCA reduced both basal and PiC +- CDCA-induced IL-8 production. Chenodeoxycholic Acid 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 28554966-9 2017 While PiC and CDCA increased IL-8 production, LCA reduced both basal and PiC +- CDCA-induced IL-8 production. Lithocholic Acid 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 28554966-9 2017 While PiC and CDCA increased IL-8 production, LCA reduced both basal and PiC +- CDCA-induced IL-8 production. pic + 73-78 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 28554966-9 2017 While PiC and CDCA increased IL-8 production, LCA reduced both basal and PiC +- CDCA-induced IL-8 production. Chenodeoxycholic Acid 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 28496415-10 2017 The activation of the MAPK/NF-kappaB signaling and induction of IL-8 to both CSE types were suppressed to similar levels by NAC, AMTB, or EGTA. Acetylcysteine 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 28496415-10 2017 The activation of the MAPK/NF-kappaB signaling and induction of IL-8 to both CSE types were suppressed to similar levels by NAC, AMTB, or EGTA. adenosylmethionine tosylate bis(sulfate) 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 28496415-10 2017 The activation of the MAPK/NF-kappaB signaling and induction of IL-8 to both CSE types were suppressed to similar levels by NAC, AMTB, or EGTA. Egtazic Acid 138-142 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 28496415-12 2017 We also found that menthol combined with Non-M-CSE induced greater responses of intracellular Ca2+ and IL-8 compared with Non-M-CSE alone. Menthol 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 28238931-0 2017 Effect of interleukin (IL)-8 on benzo[a]pyrene metabolism and DNA damage in human lung epithelial cells. Benzo(a)pyrene 32-46 C-X-C motif chemokine ligand 8 Homo sapiens 10-28 28425504-5 2017 Mechanistically, chaetocin reduced the SUV39H1 and H3K9me3 levels in the native IL-8 promoter in normal HSAEpCs, which mimicked unstimulated COPD HSAEpCs and led to decreased HP-1alpha levels and increased RNA polymerase II levels. chaetocin 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 28416823-15 2017 Using cDNA microarray we found that the expression of a panel of invasion/metastasis-related genes was significantly changed, including the increased expression of interleukin (IL)-8 and matrix metalloproteinase-3 (MMP-3) after ATP treatment. Adenosine Triphosphate 228-231 C-X-C motif chemokine ligand 8 Homo sapiens 164-182 28238931-2 2017 To elucidate the role of the inflammatory cytokine IL-8 in this process, we studied its effect on the activation and deactivation of the chemical mutagen benzo[a]pyrene B[a]P in the immortalized pulmonary BEAS-2B cell line. pyrene b 162-170 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 28238931-4 2017 Consistent with these findings, we observed higher concentration of the metabolite B[a]P-7,8-diol under concurrent IL-8 treatment conditions. 7,8-diol 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 28238931-6 2017 IL-8 lowered the intracellular NADPH level, but this effect could not explain the changes in B[a]P metabolism. NADP 31-36 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 28238931-7 2017 IL-8 also significantly depleted intracellular glutathione (GSH), which also resulted in enhanced levels of unmetabolized B[a]P, but increased concentrations of the metabolite B[a]P-7,8-diol. Glutathione 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 28238931-7 2017 IL-8 also significantly depleted intracellular glutathione (GSH), which also resulted in enhanced levels of unmetabolized B[a]P, but increased concentrations of the metabolite B[a]P-7,8-diol. Glutathione 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 28238931-7 2017 IL-8 also significantly depleted intracellular glutathione (GSH), which also resulted in enhanced levels of unmetabolized B[a]P, but increased concentrations of the metabolite B[a]P-7,8-diol. 7,8-diol 182-190 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 28238931-9 2017 These findings suggest that IL-8 increased the formation of B[a]P-7,8-diol despite an overall delayed B[a]P metabolism via depletion of GSH, but DNA damage levels were unaffected due to an increase in NER capacity. Benzo(a)pyrene 60-65 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 28238931-9 2017 These findings suggest that IL-8 increased the formation of B[a]P-7,8-diol despite an overall delayed B[a]P metabolism via depletion of GSH, but DNA damage levels were unaffected due to an increase in NER capacity. 7,8-diol 66-74 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 28238931-9 2017 These findings suggest that IL-8 increased the formation of B[a]P-7,8-diol despite an overall delayed B[a]P metabolism via depletion of GSH, but DNA damage levels were unaffected due to an increase in NER capacity. Glutathione 136-139 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 28388885-9 2017 After pre-treatment with Cytochalasin D alone, IL-8 expression and JNK phosphorylation levels were not significantly different at 6 h but were significantly increased by approximately 1.2-fold (1.18 +- 0.05; P<0.01) and 3.0-fold (3.01 +- 0.02; P<0.01) at 24 h, respectively. Cytochalasin D 25-39 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 28383530-9 2017 Decarine showed anti-inflammatory activity on human colon cells by reducing IL-6 and IL-8 production in TNF-alpha+IL-1beta-induced Caco-2 cells. Decarine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 28772744-5 2017 Sodium fluoride (NaF), which has been widely used as a desensitizing agent, is regarded as positive control. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 28101847-1 2017 We have found that a well-characterized P2X7 receptor antagonist AZ11645373 blocked production of pro-inflammatory chemokine IL-8 in endothelial cells treated with OxPAPC. AZ 11645373 65-75 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 28074216-6 2017 The results showed that increasing the concentration of ADO effectively restored the LPS-inhibited neutrophil chemotaxis to IL-8. Adenosine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 28052863-5 2017 Poly(I:C) increased the production of IL-6, IL-8, monocyte chemoattractant protein-1, and ICAM-1. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 28299617-6 2017 In particular, methyl caffeate down-regulated SASP factors such as IL-1alpha, IL-1beta, IL-6, IL-8, GM-CSF, CXCL1, MCP-2, and MMP-3. methyl caffeate 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 27896541-4 2017 Gomisin N inhibited interleukin (IL)-6, IL-8, CC chemokine ligand (CCL) 2, and CCL20 production in TNF-alpha-stimulated HPDLC in a dose-dependent manner. schizandrin B 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 28101847-1 2017 We have found that a well-characterized P2X7 receptor antagonist AZ11645373 blocked production of pro-inflammatory chemokine IL-8 in endothelial cells treated with OxPAPC. oxidized-L-alpha-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine 164-170 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 28101847-6 2017 The inhibitory action of AZ11645373 was observed at the level of IL-8 protein and messenger RNA (mRNA) induction. AZ 11645373 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 28101847-7 2017 Furthermore, AZ11645373 inhibited induction of mRNA encoding for COX-2 (PTGS2) suggesting that its anti-inflammatory potential is not limited to suppression of IL-8 production. AZ 11645373 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 28101847-8 2017 In addition to inhibiting stimulation by OxPAPC, AZ11645373 suppressed induction of IL-8 by TNFalpha and LPS. AZ 11645373 49-59 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 27397896-8 2017 RESULTS: High glucose stimulated a significant increase in the production of IL-6 and IL-8 by HGFs compared with normal glucose. Glucose 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 28349908-11 2017 Miswak impregnated with 0.5% NaF resulted in a higher concentration of fluoride in saliva than brushing with 1450 ppm fluoride toothpaste. Fluorides 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 28349908-12 2017 CLINICAL SIGNIFICANCE: Miswak impregnated with 0.5% NaF and toothbrushing results in comparable plaque removal and about the same fluoride concentration in saliva even it was somewhat higher for impregnated miswak. Fluorides 130-138 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 27397896-10 2017 When both LPS and AGE-BSA were present, especially at high concentrations (>= 500 mug/mL of LPS and >= 25 mug/mL of AGE-BSA), a synergistic effect on IL-8 production was found in the high-glucose condition. Glucose 194-201 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 27965148-4 2017 The up-regulation of ATF3 and IL-8, or DNAJB4 and GCLM induced by the representative sensitizer 2,4-dinitrochlorobenzene in human keratinocytes was significantly suppressed by a P2X7 specific antagonist KN-62, or by Nrf2 siRNA, respectively, which supported mechanistic relevance of marker genes. Dinitrochlorobenzene 96-120 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 27397896-11 2017 CONCLUSIONS: A synergistic effect of the production of IL-8 could be induced in HGFs with the combination of high glucose, LPS and AGEs. Glucose 114-121 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 28089818-9 2017 Enzyme-linked immunosorbent assay results revealed distinct differences in IL-6 and IL-8 secretions by NP cells in response to etoposide in the presence of NCCM. Etoposide 127-136 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 28315997-6 2017 Ruminant TFA, including tVA, tPA and the mixture of tVA and tPA, significantly reduced the TNF-alpha-induced gene expression of TNF, VCAM-1 and SOD2 in HUVEC, as well as TNF and IL-8 in HepG2 cells. Trans Fatty Acids 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 28315997-6 2017 Ruminant TFA, including tVA, tPA and the mixture of tVA and tPA, significantly reduced the TNF-alpha-induced gene expression of TNF, VCAM-1 and SOD2 in HUVEC, as well as TNF and IL-8 in HepG2 cells. 11-octadecenoic acid 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 28315997-6 2017 Ruminant TFA, including tVA, tPA and the mixture of tVA and tPA, significantly reduced the TNF-alpha-induced gene expression of TNF, VCAM-1 and SOD2 in HUVEC, as well as TNF and IL-8 in HepG2 cells. palmitoleic acid 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 28315997-6 2017 Ruminant TFA, including tVA, tPA and the mixture of tVA and tPA, significantly reduced the TNF-alpha-induced gene expression of TNF, VCAM-1 and SOD2 in HUVEC, as well as TNF and IL-8 in HepG2 cells. palmitoleic acid 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 28259918-2 2017 The plasmid vector containing CXCL8 cDNA was transfected into LoVo cells using Lipofectamine 2000 reagent. lipofectamine 2000 reagent 79-105 C-X-C motif chemokine ligand 8 Homo sapiens 30-35 28078769-8 2017 IL-1alpha induced IL-8 in bronchial epithelial cells, which was dose-dependently inhibited by dexamethasone but not by azithromycin. Dexamethasone 94-107 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 28078769-12 2017 We established an in vitro model wherein steroids inhibit the IL-1alpha-induced IL-8 production, while azithromycin was ineffective. Steroids 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 30090515-7 2017 In addition, ATF2 knockdown did not decrease the expressions of pro-inflammatory cytokines induced by arsenite in SV-HUC-1 cells, but dramatically increased mRNA expressions of TNFalpha, TGFalpha and IL-8 under arsenite and non-arsenite conditions. arsenite 211-219 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 30090515-7 2017 In addition, ATF2 knockdown did not decrease the expressions of pro-inflammatory cytokines induced by arsenite in SV-HUC-1 cells, but dramatically increased mRNA expressions of TNFalpha, TGFalpha and IL-8 under arsenite and non-arsenite conditions. arsenite 211-219 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 28344983-10 2017 Challenge with bile acids at physiological levels also led to a significant increase in the release of IL-8 and IL6 from BEAS-2B. Bile Acids and Salts 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 28167529-4 2017 Suppression or neutralization of vorinostat-induced IL-8/CXCL8 potentiates the vorinostat inhibitory effect on cell viability and proliferation. Vorinostat 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 57-62 28167529-4 2017 Suppression or neutralization of vorinostat-induced IL-8/CXCL8 potentiates the vorinostat inhibitory effect on cell viability and proliferation. Vorinostat 79-89 C-X-C motif chemokine ligand 8 Homo sapiens 57-62 28167529-5 2017 The IL-8/CXCL8 expression induced by vorinostat in EOC cells is dependent on IkappaB kinase (IKK) activity and associated with a gene-specific recruitment of IKKbeta and IKK-dependent recruitment of p65 NFkappaB to the IL-8/CXCL8 promoter. Vorinostat 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 9-14 28167529-5 2017 The IL-8/CXCL8 expression induced by vorinostat in EOC cells is dependent on IkappaB kinase (IKK) activity and associated with a gene-specific recruitment of IKKbeta and IKK-dependent recruitment of p65 NFkappaB to the IL-8/CXCL8 promoter. Vorinostat 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 224-229 28345644-5 2017 Vitamin D had no effect on BEAS-2B cells but enhanced the production of IL-8 in neutrophils (p = 0.007) and IL-1beta in macrophages (p = 0.007) in response to LPS. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 28189686-0 2017 Interleukin-8 enhances the effect of colchicine on cell death. Colchicine 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 28189686-6 2017 The effect of colchicine on cell death was enhanced in cells overexpressing IL-8. Colchicine 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 28189686-7 2017 Moreover, the effect of colchicine on cell death was enhanced in cells overexpressing two IL-8 up-regulators, NF-kappaB and IL-6, but not in cells overexpressing an IL-8 down-regulator, splicing factor proline/glutamine-rich (SFPQ). Colchicine 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28189686-8 2017 Synergistic effects of IL-8 and colchicine were also observed in cells overexpressing IL-8 isoforms lacking the signal peptide. Colchicine 32-42 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 28189686-9 2017 Therefore, IL-8 appeared to function as an enhancer of cell death in cancer cells treated with colchicine. Colchicine 95-105 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 28278187-6 2017 Treatment with resveratrol significantly reduced the expression and secretion of pro-inflammatory cytokines IL-6, IL-1alpha, IL-1beta and pro-inflammatory chemokines IL-8 and MCP-1 in human placenta and omental and subcutaneous adipose tissue. Resveratrol 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 28323848-7 2017 These results indicate that 7-oxygenated cholesterol derivatives have differential effects on monocyte/macrophage expression of IL-8 and C5a receptor and that C5a receptor is involved in 7alphaOHChol-induced IL-8 expression via PI3K and MEK. Cholesterol 41-52 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 28323848-7 2017 These results indicate that 7-oxygenated cholesterol derivatives have differential effects on monocyte/macrophage expression of IL-8 and C5a receptor and that C5a receptor is involved in 7alphaOHChol-induced IL-8 expression via PI3K and MEK. 7alphaohchol 187-199 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 27997850-1 2017 Here a simple yet cost-effective strategy is developed to fabricate fluorine-doped graphene nanosheets, we successfully, prepared fluorine doped graphene via thermal treatment of graphene oxide and NaF (sodium fluoride) in H2SO4 solution phase. Fluorine 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 198-201 27997850-1 2017 Here a simple yet cost-effective strategy is developed to fabricate fluorine-doped graphene nanosheets, we successfully, prepared fluorine doped graphene via thermal treatment of graphene oxide and NaF (sodium fluoride) in H2SO4 solution phase. Graphite 83-91 C-X-C motif chemokine ligand 8 Homo sapiens 198-201 27997850-1 2017 Here a simple yet cost-effective strategy is developed to fabricate fluorine-doped graphene nanosheets, we successfully, prepared fluorine doped graphene via thermal treatment of graphene oxide and NaF (sodium fluoride) in H2SO4 solution phase. fluorine doped 130-144 C-X-C motif chemokine ligand 8 Homo sapiens 198-201 27997850-1 2017 Here a simple yet cost-effective strategy is developed to fabricate fluorine-doped graphene nanosheets, we successfully, prepared fluorine doped graphene via thermal treatment of graphene oxide and NaF (sodium fluoride) in H2SO4 solution phase. Graphite 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 198-201 27997850-1 2017 Here a simple yet cost-effective strategy is developed to fabricate fluorine-doped graphene nanosheets, we successfully, prepared fluorine doped graphene via thermal treatment of graphene oxide and NaF (sodium fluoride) in H2SO4 solution phase. Sodium Fluoride 203-218 C-X-C motif chemokine ligand 8 Homo sapiens 198-201 27997850-1 2017 Here a simple yet cost-effective strategy is developed to fabricate fluorine-doped graphene nanosheets, we successfully, prepared fluorine doped graphene via thermal treatment of graphene oxide and NaF (sodium fluoride) in H2SO4 solution phase. sulfuric acid 223-228 C-X-C motif chemokine ligand 8 Homo sapiens 198-201 28323848-0 2017 7alpha-Hydroxycholesterol induces monocyte/macrophage cell expression of interleukin-8 via C5a receptor. cholest-5-en-3 beta,7 alpha-diol 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 28323848-2 2017 Transcript levels of IL-8 and secretion of its corresponding gene product by monocytes/macrophages were enhanced by treatment with 7alphaOHChol and, to a lesser extent, 7K, but not by 7betaOHChol. 7alphaohchol 131-143 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 28323848-2 2017 Transcript levels of IL-8 and secretion of its corresponding gene product by monocytes/macrophages were enhanced by treatment with 7alphaOHChol and, to a lesser extent, 7K, but not by 7betaOHChol. 7betaohchol 184-195 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 28323848-4 2017 7alphaOHChol-induced IL-8 gene transcription was inhibited by cycloheximide and Akt1 downregulation, but not by OxPAPC. 7alphaohchol 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 28323848-4 2017 7alphaOHChol-induced IL-8 gene transcription was inhibited by cycloheximide and Akt1 downregulation, but not by OxPAPC. Cycloheximide 62-75 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 28323848-5 2017 Expression of C5a receptor was upregulated after stimulation with 7alphaOHChol, but not with 7K and 7betaOHChol, and a specific antagonist of C5a receptor inhibited 7alphaOHChol-induced IL-8 gene expression in a dose dependent manner. 7alphaohchol 66-78 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 28323848-5 2017 Expression of C5a receptor was upregulated after stimulation with 7alphaOHChol, but not with 7K and 7betaOHChol, and a specific antagonist of C5a receptor inhibited 7alphaOHChol-induced IL-8 gene expression in a dose dependent manner. 7alphaohchol 165-177 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 28323848-6 2017 Pharmacological inhibitors of PI3K and MEK almost completely inhibited expression of both IL-8 and cell-surface C5a receptor induced by 7alphaOHChol. 7alphaohchol 136-148 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28323848-7 2017 These results indicate that 7-oxygenated cholesterol derivatives have differential effects on monocyte/macrophage expression of IL-8 and C5a receptor and that C5a receptor is involved in 7alphaOHChol-induced IL-8 expression via PI3K and MEK. Cholesterol 41-52 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 28386331-4 2017 We devised this study to determine whether Hcy could affect the expression and secretion of VEGF and IL-8 from EPCs. Homocysteine 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 28386331-5 2017 We found that high levels of Hcy (100-500 muM) decreased the EPC-mediated protein secretion and mRNA expression of VEGF and IL-8. Homocysteine 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 28081470-7 2017 The expression level of cytokines and chemokines influenced by eleutheroside B1 was further demonstrated, the IL-6, CXCL-8, CCL-2 expression were all inhibited by the eleuthe roside B1 at concentration 200mug/ml. Eleutheroside B1 63-79 C-X-C motif chemokine ligand 8 Homo sapiens 116-122 28003224-5 2017 We found that a corticosteroid (methylprednisolone) and an anti-VEGF agent (bevacizumab) prevented mCRP-induced ARPE-19 barrier disruption and IL-8 production. Methylprednisolone 32-50 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 28337465-8 2017 Acetoin and diacetyl treatment induced IL-8 release in Beas2B cells. Acetoin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 28337465-8 2017 Acetoin and diacetyl treatment induced IL-8 release in Beas2B cells. Diacetyl 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 28337465-9 2017 Acetoin- and pentanedione-treated HFL-1 cells produced a differential, but significant response for IL-8 release compared to controls and TNFalpha. Acetoin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 28337465-9 2017 Acetoin- and pentanedione-treated HFL-1 cells produced a differential, but significant response for IL-8 release compared to controls and TNFalpha. acetylacetone 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 28337465-10 2017 Flavorings, such as ortho-vanillin and maltol, induced IL-8 release in Beas2B cells, but not in H292 cells. vanillin 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 28337465-10 2017 Flavorings, such as ortho-vanillin and maltol, induced IL-8 release in Beas2B cells, but not in H292 cells. maltol 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 28337465-11 2017 Of all the flavoring chemicals tested, acetoin and maltol were more potent inducers of IL-8 release than TNFalpha in Beas2B and HFL-1 cells. Acetoin 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 28337465-11 2017 Of all the flavoring chemicals tested, acetoin and maltol were more potent inducers of IL-8 release than TNFalpha in Beas2B and HFL-1 cells. maltol 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 28081470-7 2017 The expression level of cytokines and chemokines influenced by eleutheroside B1 was further demonstrated, the IL-6, CXCL-8, CCL-2 expression were all inhibited by the eleuthe roside B1 at concentration 200mug/ml. eleuthe roside b1 167-184 C-X-C motif chemokine ligand 8 Homo sapiens 116-122 28013079-5 2017 We found that the responses of AP-1, BTG2, and IL8 biosensors in assessing the toxicity of silver nanoparticles (Ag NPs) showed good dose-related increases after exposure to Ag NPs and were consistent with data acquired by conventional assays, such as western blot, real-time polymerase chain reaction, and immunofluorescence. Silver 91-97 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 27913196-10 2017 In addition, miR-155, IL-6, and IL-8 were over-expressed in the serum of arsenite exposure group. arsenite 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 27651218-8 2017 RESULTS: After 12 weeks of rimonabant treatment, there was a significant increase in VEGF (99 2 +- 17 6 vs 116 2 +- 15 8 pg/ml, P < 0 01) and IL-8 (7 4 +- 11 0 vs 18 1 +- 13 2 pg/ml, P < 0 05) but not after metformin (VEGF P = 0 7; IL-8 P = 0 9). Rimonabant 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 27651218-8 2017 RESULTS: After 12 weeks of rimonabant treatment, there was a significant increase in VEGF (99 2 +- 17 6 vs 116 2 +- 15 8 pg/ml, P < 0 01) and IL-8 (7 4 +- 11 0 vs 18 1 +- 13 2 pg/ml, P < 0 05) but not after metformin (VEGF P = 0 7; IL-8 P = 0 9). Rimonabant 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 27651218-10 2017 CONCLUSION: This study suggests that rimonabant CB-I blockade paradoxically raised VEGF and the cytokine IL-8 in obese women with PCOS that may have offset the potential benefit associated with weight loss. cobinamide 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 28314697-5 2017 Upon FXa stimulation, the expressions of pro-inflammatory genes such as monocyte chemoattractant protein-1 (MCP-1), intracellular adhesion molecule-1, and interleukin-8 were maximally increased at 4 h after stimulation, and were suppressed by rivaroxaban. Rivaroxaban 243-254 C-X-C motif chemokine ligand 8 Homo sapiens 155-168 27719921-7 2017 Betalains dampened cyclooxygenase-2 and interleukin-8 mRNA expression after lipopolysaccharide induction in CaCo-2, showing an anti-inflammatory action. Betalains 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 28204809-0 2017 Ketamine suppresses the substance P-induced production of IL-6 and IL-8 by human U373MG glioblastoma/astrocytoma cells. Ketamine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 28204809-5 2017 The results from our experiments indicated that ketamine suppressed the production of interleukin (IL)-6 and IL-8 by the U373MG cells. Ketamine 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 28204809-7 2017 Taken together, these observations suggest that ketamine may suppress the SP-induced activation (IL-6 and IL-8 production) of U373MG cells by inhibiting the phosphorylation of signaling molecules (namely ERK1/2, p38 MAPK and NF-kappaB), thereby exerting anti-inflammatory effects. Ketamine 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 28454334-0 2017 Taxotere-induced elevated expression of IL8 in carcinoma-associated fibroblasts of breast invasive ductal cancer. Docetaxel 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 26826259-7 2017 Glutamine, arginine, and vitamin D3, but not ALA, significantly attenuated IL-8 production. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 26826259-7 2017 Glutamine, arginine, and vitamin D3, but not ALA, significantly attenuated IL-8 production. Arginine 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 26826259-7 2017 Glutamine, arginine, and vitamin D3, but not ALA, significantly attenuated IL-8 production. Cholecalciferol 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 26826259-9 2017 Combining glutamine, arginine, and curcumin at optimal concentrations completely abolished the IL-8 response. Glutamine 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 26826259-9 2017 Combining glutamine, arginine, and curcumin at optimal concentrations completely abolished the IL-8 response. Arginine 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 26826259-9 2017 Combining glutamine, arginine, and curcumin at optimal concentrations completely abolished the IL-8 response. Curcumin 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 28454334-9 2017 Overall, elevated expression of IL8 induced by Taxotere in CAFs potentially supports the association between IL8 and chemotherapy response. cafs 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 28454334-8 2017 It was observed that the expression of the candidate gene IL8 in the CAFs of breast invasive cancer following treatment with Taxotere was increased (P<0.05). cafs 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 28454334-8 2017 It was observed that the expression of the candidate gene IL8 in the CAFs of breast invasive cancer following treatment with Taxotere was increased (P<0.05). Docetaxel 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 28454334-9 2017 Overall, elevated expression of IL8 induced by Taxotere in CAFs potentially supports the association between IL8 and chemotherapy response. Docetaxel 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 28454334-9 2017 Overall, elevated expression of IL8 induced by Taxotere in CAFs potentially supports the association between IL8 and chemotherapy response. Docetaxel 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 28454334-9 2017 Overall, elevated expression of IL8 induced by Taxotere in CAFs potentially supports the association between IL8 and chemotherapy response. cafs 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 27444775-7 2017 RESULTS: The gene expression and protein secretion of IL-8 in endometriotic stromal cells after incubation with lignocaine 0.1 mg/mL were significantly decreased after 24 hours compared to the controls ( P = .028 and P = .018). Lidocaine 112-122 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 28087464-5 2017 Furthermore, the mitochondrial ROS scavenger Mito-TEMPO, which inhibited MAPK and AP-1, significantly reduced MCP-1 and IL-1beta mRNA expression and reduced HL-60 cell migration through the suppression of MCP-1 and IL-8 protein secretion. Reactive Oxygen Species 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 29250282-6 2017 Results: Immediate post ablation levels of inflammatory cytokines were lower in the steroid group when compared to the placebo group; IL-6: 9.0 +-7 vs 15.8 +-13 p=0.031; IL-8: 10.5 +-9 vs 15.3 +-8; p=0.047 respectively. Steroids 84-91 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 28106172-0 2017 Carrageenan activates monocytes via type-specific binding with interleukin-8: an implication for design of immuno-active biomaterials. Carrageenan 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 28082672-5 2017 We show here that in both squamous cell carcinoma cells and melanoma tumor cells, CQ induced NF-kappaB activation and the expression of its target genes HIF-1alpha, IL-8, BCL-2, and BCL-XL through the accumulation of autophagosomes, p62, and JNK signaling. Chloroquine 82-84 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 28230729-1 2017 Chlorogenic acid (CHA) and caffeic acid (CA) are phenolic compounds found in coffee, which inhibit oxidative stress-induced interleukin (IL)-8 production in intestinal epithelial cells, thereby suppressing serious cellular injury and inflammatory intestinal diseases. caffeic acid 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 124-142 28235416-8 2017 RESULTS: Pretreatment with low-dose (1 or 5 muM), long-term (72 h) CAM inhibited H2O2-induced IL-8 levels, NF-kappaB activity, and IL-8 mRNA expression, and improved the GSH/GSSG ratio via the maintenance of gamma-GCS expression levels. Clarithromycin 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 28235416-8 2017 RESULTS: Pretreatment with low-dose (1 or 5 muM), long-term (72 h) CAM inhibited H2O2-induced IL-8 levels, NF-kappaB activity, and IL-8 mRNA expression, and improved the GSH/GSSG ratio via the maintenance of gamma-GCS expression levels. Clarithromycin 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 28235416-8 2017 RESULTS: Pretreatment with low-dose (1 or 5 muM), long-term (72 h) CAM inhibited H2O2-induced IL-8 levels, NF-kappaB activity, and IL-8 mRNA expression, and improved the GSH/GSSG ratio via the maintenance of gamma-GCS expression levels. Hydrogen Peroxide 81-85 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 28231837-8 2017 RESULTS: PBMCs from nAMD patients secreted higher levels of IL-8, CCL2 and VEGF, especially following LPS and 1% oxygen stimulation, than those from controls. Oxygen 113-119 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 28260873-10 2017 COPD patients with CRS had a higher percentage of eosinophils, higher levels of IL-8, IL-6, and MMP-9 in sputum as compared to those without CRS. 3-cresol 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 28251074-8 2017 LPS at concentrations of 300 ng/mL for 1h significantly stimulated the mRNA expression of IL-8, IL-6, IL-1beta, TNF-alpha, and TGF-beta in HCECs, while the stimulation effects were significantly inhibited by AA (20 micromol/L). Hydrogen 39-41 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28055957-6 2017 Furthermore, 5-FU significantly induced c-Jun N-terminal kinase (JNK) activation and the expression of pro-inflammatory genes IL-8 and ICAM-1. Fluorouracil 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 28230729-0 2017 Catechol Groups Enable Reactive Oxygen Species Scavenging-Mediated Suppression of PKD-NFkappaB-IL-8 Signaling Pathway by Chlorogenic and Caffeic Acids in Human Intestinal Cells. catechol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 28230729-0 2017 Catechol Groups Enable Reactive Oxygen Species Scavenging-Mediated Suppression of PKD-NFkappaB-IL-8 Signaling Pathway by Chlorogenic and Caffeic Acids in Human Intestinal Cells. Reactive Oxygen Species 23-46 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 28230729-0 2017 Catechol Groups Enable Reactive Oxygen Species Scavenging-Mediated Suppression of PKD-NFkappaB-IL-8 Signaling Pathway by Chlorogenic and Caffeic Acids in Human Intestinal Cells. Caffeic Acids 137-150 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 28230729-1 2017 Chlorogenic acid (CHA) and caffeic acid (CA) are phenolic compounds found in coffee, which inhibit oxidative stress-induced interleukin (IL)-8 production in intestinal epithelial cells, thereby suppressing serious cellular injury and inflammatory intestinal diseases. Chlorogenic Acid 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 124-142 28230729-1 2017 Chlorogenic acid (CHA) and caffeic acid (CA) are phenolic compounds found in coffee, which inhibit oxidative stress-induced interleukin (IL)-8 production in intestinal epithelial cells, thereby suppressing serious cellular injury and inflammatory intestinal diseases. Chlorogenic Acid 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 124-142 28230729-2 2017 Therefore, we investigated the anti-inflammatory mechanism of CHA and CA, both of which inhibited hydrogen peroxide (H2O2)-induced IL-8 transcriptional activity. Chlorogenic Acid 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 28230729-2 2017 Therefore, we investigated the anti-inflammatory mechanism of CHA and CA, both of which inhibited hydrogen peroxide (H2O2)-induced IL-8 transcriptional activity. Hydrogen Peroxide 98-115 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 28230729-2 2017 Therefore, we investigated the anti-inflammatory mechanism of CHA and CA, both of which inhibited hydrogen peroxide (H2O2)-induced IL-8 transcriptional activity. Hydrogen Peroxide 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 28230729-6 2017 Therefore, we conclude that the presence of catechol groups in CHA and CA allows scavenging of intracellular ROS, thereby inhibiting H2O2-induced IL-8 production via suppression of PKD-NF-kappaB signaling in human intestinal epithelial cells. catechol 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 28230729-6 2017 Therefore, we conclude that the presence of catechol groups in CHA and CA allows scavenging of intracellular ROS, thereby inhibiting H2O2-induced IL-8 production via suppression of PKD-NF-kappaB signaling in human intestinal epithelial cells. Reactive Oxygen Species 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 28230729-6 2017 Therefore, we conclude that the presence of catechol groups in CHA and CA allows scavenging of intracellular ROS, thereby inhibiting H2O2-induced IL-8 production via suppression of PKD-NF-kappaB signaling in human intestinal epithelial cells. Hydrogen Peroxide 133-137 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 28178959-14 2017 CONCLUSION: IL-8 is a target to explore further as a predictor of 28 days mortality, in patients with AHRF treated with NPPV. nppv 120-124 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 27940299-4 2017 Moreover, like E2 and G1, Cd leads to a rapid activation of ERK/AKT, and then nuclear translocation of NF-kappaB, increased expression of cyclin A and D1, and secretion of IL-8, all of which are significantly attenuated by GPER blockage or knock-down in both WRO and FRO cells. Cadmium 26-28 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 28108387-4 2017 Pretreatment with MAO-B selective inhibitor selegiline reversed the CSM-induced changes in MAO-B activity, ROS levels and IL-8 release in a dose-dependent manner. Selegiline 44-54 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 27998979-11 2017 Dexamethasone induces the recruitment of ACTN4 and GR to putative GREs in dexamethasone-transactivated promoters, SERPINE1, ANGPLT4, CCL20, and SAA1 as well as the NF-kappaB (p65) binding sites on GR-transrepressed promoters such as IL-1beta, IL-6, and IL-8 Taken together, our data establish ACTN4 as a transcriptional co-regulator that modulates both dexamethasone-transactivated and -transrepressed genes in podocytes. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 27998979-11 2017 Dexamethasone induces the recruitment of ACTN4 and GR to putative GREs in dexamethasone-transactivated promoters, SERPINE1, ANGPLT4, CCL20, and SAA1 as well as the NF-kappaB (p65) binding sites on GR-transrepressed promoters such as IL-1beta, IL-6, and IL-8 Taken together, our data establish ACTN4 as a transcriptional co-regulator that modulates both dexamethasone-transactivated and -transrepressed genes in podocytes. Dexamethasone 74-87 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 27618139-0 2017 Significant Decrease in Plasma Levels of D-Dimer, Interleukin-8, and Interleukin-12 After a 12-Month Treatment with Rosuvastatin in HIV-Infected Patients Under Antiretroviral Therapy. Rosuvastatin Calcium 116-128 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 28058843-0 2017 Formation of a K-In-Se Surface Species by NaF/KF Postdeposition Treatment of Cu(In,Ga)Se2 Thin-Film Solar Cell Absorbers. Selenium 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 30090494-5 2017 Exposure to 50 or 200 muM paraquat for 24 h elevated the release of interleukin 8 and gene expression of tumor necrosis factor-alpha. Paraquat 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 27618139-10 2017 CONCLUSIONS: Our findings show that a 12-month treatment with rosuvastatin associated with an effective cART can significantly decrease the plasma levels of D-dimer, IL-8, and IL-12, and suggest a potential role for this statin to reduce activated coagulation and systemic inflammation among HIV-infected persons. Rosuvastatin Calcium 62-74 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 28058843-0 2017 Formation of a K-In-Se Surface Species by NaF/KF Postdeposition Treatment of Cu(In,Ga)Se2 Thin-Film Solar Cell Absorbers. Copper 77-79 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 28058843-1 2017 A NaF/KF postdeposition treatment (PDT) has recently been employed to achieve new record efficiencies of Cu(In,Ga)Se2 (CIGSe) thin film solar cells. Copper 105-107 C-X-C motif chemokine ligand 8 Homo sapiens 2-5 28006108-5 2017 The primary objective was to measure the effects of digitoxin on IL-8 and neutrophil counts in induced sputum. Digitoxin 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 28058843-5 2017 The NaF/KF-PDT, however, leads to the formation of bilayer structure in which a K-In-Se species covers the CIGSe compound that in composition is identical to the chalcopyrite structure of the alkali-free and NaF-PDT absorber. lysylphenylalanine 8-10 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 28058843-5 2017 The NaF/KF-PDT, however, leads to the formation of bilayer structure in which a K-In-Se species covers the CIGSe compound that in composition is identical to the chalcopyrite structure of the alkali-free and NaF-PDT absorber. lysylphenylalanine 8-10 C-X-C motif chemokine ligand 8 Homo sapiens 208-211 28058843-5 2017 The NaF/KF-PDT, however, leads to the formation of bilayer structure in which a K-In-Se species covers the CIGSe compound that in composition is identical to the chalcopyrite structure of the alkali-free and NaF-PDT absorber. k-in-se 80-87 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 28058843-5 2017 The NaF/KF-PDT, however, leads to the formation of bilayer structure in which a K-In-Se species covers the CIGSe compound that in composition is identical to the chalcopyrite structure of the alkali-free and NaF-PDT absorber. chalcopyrite 162-174 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 27796814-14 2017 Interleukin-8 may be an important mediator for hepatic fibrosis in nonalcoholic fatty liver disease patients with low vitamin D status. Vitamin D 118-127 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 26965496-8 2017 Global proteome analysis showed that the NRF2-mediated stress response and the CXCL8 (IL-8) pathway were induced by ketoconazole treatment under co-culture conditions. Ketoconazole 116-128 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 26965496-8 2017 Global proteome analysis showed that the NRF2-mediated stress response and the CXCL8 (IL-8) pathway were induced by ketoconazole treatment under co-culture conditions. Ketoconazole 116-128 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 26965496-9 2017 The upregulation and ketoconazole-induced secretion of several pro-inflammatory cytokines, including CXCL8, TNF-alpha and CCL3, was observed in the co-culture system only, but not in single cell cultures. Ketoconazole 21-33 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 27879488-0 2017 18F-NaF PET Demonstrating Unusual Focal Tracer Activity in the Brain. Fluorine-18 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 27863334-7 2017 Conversely, in phorbol 12-myristate 13-acetate and ionomycin (PMA/Io) stimulated Caco-2 cells, lactobacilli from the omnivorous group and all bifidobacteria significantly down-regulated IL-8. Tetradecanoylphorbol Acetate 15-46 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 27863334-7 2017 Conversely, in phorbol 12-myristate 13-acetate and ionomycin (PMA/Io) stimulated Caco-2 cells, lactobacilli from the omnivorous group and all bifidobacteria significantly down-regulated IL-8. Ionomycin 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 27863334-7 2017 Conversely, in phorbol 12-myristate 13-acetate and ionomycin (PMA/Io) stimulated Caco-2 cells, lactobacilli from the omnivorous group and all bifidobacteria significantly down-regulated IL-8. Tetradecanoylphorbol Acetate 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 27988459-4 2017 One of these derivatives, (Z)-2-((5-(hydroxymethyl) furan-2-yl) methylene) benzofuran-3(2H)-one (aurone 1), was found to inhibit LPS-induced secretion of the pro-inflammatory cytokines, tumor-necrosis factor alpha (TNFalpha), interleukin 1beta (IL-1beta), and IL-8 by THP-1 cells. (z)-2-((5-(hydroxymethyl) furan-2-yl) methylene) benzofuran-3(2h)-one 26-95 C-X-C motif chemokine ligand 8 Homo sapiens 260-264 28013186-7 2017 RESULTS: Treatment with PT or PO inhibited the secretion of interleukin (IL)-8 and tumor necrosis factor (TNF) in ethanol- or LPS-stimulated KATO III cells. Ethanol 114-121 C-X-C motif chemokine ligand 8 Homo sapiens 60-78 27966575-8 2017 The combined group of vitamin D2 and D3 treated patients decreased plasma IL-8 (P<0.05). Ergocalciferols 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 27966575-8 2017 The combined group of vitamin D2 and D3 treated patients decreased plasma IL-8 (P<0.05). Cholecalciferol 37-39 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 27739345-0 2017 Rosuvastatin Inhibits Interleukin (IL)-8 and IL-6 Production in Human Coronary Artery Endothelial Cells Stimulated With Aggregatibacter actinomycetemcomitans Serotype b. Rosuvastatin Calcium 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 22-40 27186953-5 2017 Unexpectedly, NaW further induced IL-6, IL-8, and MCP-1 secretion in both N- and D-RPTEC, together with lower levels of IL-1 RA, IL-4, IL-10, and GM-CSF, suggesting that it may contribute to the extent of renal damage/repair during DKD. naw 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 28000839-9 2017 IL-6 and IL-8 expression was inhibited completely by treatment with the NF-kappaB inhibitor, BAY11-7082. 3-(4-methylphenylsulfonyl)-2-propenenitrile 93-103 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 28035387-10 2017 Additionally, levels of IL-6 and IL-8 were significantly decreased by prednisone, ibuprofen and betamethasone. Prednisone 70-80 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 28067893-0 2017 Vemurafenib and trametinib reduce expression of CTGF and IL-8 in V600EBRAF melanoma cells. Vemurafenib 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 28067893-0 2017 Vemurafenib and trametinib reduce expression of CTGF and IL-8 in V600EBRAF melanoma cells. trametinib 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 28067893-11 2017 Interestingly, expression of IL-8 and CTGF was significantly reduced by treatment with vemurafenib and trametinib. Vemurafenib 87-98 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 28067893-11 2017 Interestingly, expression of IL-8 and CTGF was significantly reduced by treatment with vemurafenib and trametinib. trametinib 103-113 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 28064076-7 2017 Drospirenone significantly decreased IL-6, IL-8, VEGF and NGF mRNA expression by ESC. drospirenone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 28064076-8 2017 Drospirenone (10-5M) significantly decreased IL-6 secretion and 10-7M drospirenone decreased IL-8 and VEGF secretion. drospirenone 70-82 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 28151872-2 2017 The aim of this study was to elucidate whether serum levels of IL-6 and IL-8 at diagnosis could predict the tumor progression pattern of PDAC, especially in extensive hepatic metastasis.According to the tumor burden of hepatic metastasis at the last follow-up, tumor progression pattern was defined as follows: no or limited (unilobar involvement and 5 or less in the within liver, limited group) and extensive hepatic metastasis (bilobar or more than 5, progressed group). pdac 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 28035387-12 2017 In combination with IL-6 or IL-8, prednisone, ibuprofen and betamethasone significantly reduced the levels of collagen I, MMP-1 and MMP-13, and inactivated NF-kappaB and STAT3 pathways. Betamethasone 60-73 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 28035387-13 2017 In conclusion, prednisone, ibuprofen and betamethasone may prevent OA by suppressing the expression of IL-6 and IL-8, subsequently inactivating NF-kappaB and STAT3 pathways, and ultimately, leading to decreased levels of collagen I, MMP-1, and MMP-13. Prednisone 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 28035387-10 2017 Additionally, levels of IL-6 and IL-8 were significantly decreased by prednisone, ibuprofen and betamethasone. Ibuprofen 82-91 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 28035387-13 2017 In conclusion, prednisone, ibuprofen and betamethasone may prevent OA by suppressing the expression of IL-6 and IL-8, subsequently inactivating NF-kappaB and STAT3 pathways, and ultimately, leading to decreased levels of collagen I, MMP-1, and MMP-13. Ibuprofen 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 28035387-10 2017 Additionally, levels of IL-6 and IL-8 were significantly decreased by prednisone, ibuprofen and betamethasone. Betamethasone 96-109 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 28035387-13 2017 In conclusion, prednisone, ibuprofen and betamethasone may prevent OA by suppressing the expression of IL-6 and IL-8, subsequently inactivating NF-kappaB and STAT3 pathways, and ultimately, leading to decreased levels of collagen I, MMP-1, and MMP-13. Betamethasone 41-54 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 27546737-2 2017 METHODS AND RESULTS: Irisolidone and kakkalide inhibited IL-8 secretion and NF-kappaB activation in lipopolysaccharide-stimulated KATO III cells. irisolidone 21-32 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 28035387-12 2017 In combination with IL-6 or IL-8, prednisone, ibuprofen and betamethasone significantly reduced the levels of collagen I, MMP-1 and MMP-13, and inactivated NF-kappaB and STAT3 pathways. Ibuprofen 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 27546737-2 2017 METHODS AND RESULTS: Irisolidone and kakkalide inhibited IL-8 secretion and NF-kappaB activation in lipopolysaccharide-stimulated KATO III cells. kakkalide 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 27574898-7 2017 In the SW1353 cell line model, zingerone efficiently suppressed the expression of TNF-alpha, interleukin-6, and interleukin-8 mRNA levels and tended to reduce the levels of both p38 and c-Jun N-terminal kinase phosphorylation. zingerone 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 27561918-3 2017 The transported polyphenols were able to downregulate the secretion of pro-inflammatory markers, i.e. IL-8, monocyte chemoattractant protein 1, vascular endothelial growth factor, and intercellular adhesion molecule 1, under normal and tumor necrosis factor alpha induced inflammatory conditions. Polyphenols 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 28007550-9 2017 Transient changes in urothelial ATP and PGE2 release were observed, with significant increase in release of interleukin-6, interleukin-8 and interleukin-1beta from urothelial cells treated with gemcitabine. gemcitabine 194-205 C-X-C motif chemokine ligand 8 Homo sapiens 123-136 27736317-6 2017 OACs in coculture with AMs expressed significantly higher levels of MMP-1, MMP-3, MMP-9, MMP-13, IL-1beta, TNF-alpha, IL-6, IL-8, and IFN-gamma compared to OACs in mono-culture, indicating that proinflammatory macrophages may intensify the abnormal matrix degradation and cytokine secretion already associated with OACs. oacs 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 27746371-9 2017 Moreover, IL-8 production induced by PHMB was completely suppressed by a NF-kappaB inhibitor, but not by a ROS scavenger. polihexanide 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 27596523-6 2017 We also analyzed the effects of CS exposure on the inflammatory response, and observed a significant increase in secretion of IL-8, GRO-alpha, IL-1beta, and GM-CSF. Cesium 32-34 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 28118826-8 2017 Concentrations of NAC >=300 muM inhibited the inflammatory response (release of IL-1beta, IL-8, and TNF-alpha) of human airways induced by the overnight stimulation with LPS, whereas lower concentrations of NAC (>=1 muM) were sufficient to reduce the release of IL-6 elicited by LPS. Acetylcysteine 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 27913418-6 2017 Subsequently, we demonstrated that DG-EPS displays immunostimulating properties by enhancing the gene expression of the proinflammatory cytokines tumor necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6), and particularly that of the chemokines IL-8 and CCL20, in the human monocytic cell line THP-1. dg-eps 35-41 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 28004929-1 2017 23Na MAS NMR spectra of sodium-oxygen (Na-O2) cathodes reveals a combination of degradation species: newly observed sodium fluoride (NaF) and the expected sodium carbonate (Na2CO3), as well as the desired reaction product sodium peroxide (Na2O2). sodium-oxygen (na-o2) cathodes 24-54 C-X-C motif chemokine ligand 8 Homo sapiens 133-136 28004929-1 2017 23Na MAS NMR spectra of sodium-oxygen (Na-O2) cathodes reveals a combination of degradation species: newly observed sodium fluoride (NaF) and the expected sodium carbonate (Na2CO3), as well as the desired reaction product sodium peroxide (Na2O2). Sodium Fluoride 116-131 C-X-C motif chemokine ligand 8 Homo sapiens 133-136 28004929-3 2017 The reactivity of solid NaO2 is probed further, and NaF is found to be formed through a reaction between the electrochemically generated NaO2 and the electrode binder, polyvinylidene fluoride (PVDF). NaO2 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 28107509-6 2017 RESULTS: Exposing the 3D models to Pd nanoparticles induced increased secretion of IL-8, yet the chronic bronchitis-like model released significantly more IL-8 than the normal model. Palladium 35-37 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 28107509-6 2017 RESULTS: Exposing the 3D models to Pd nanoparticles induced increased secretion of IL-8, yet the chronic bronchitis-like model released significantly more IL-8 than the normal model. Palladium 35-37 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 28149283-7 2016 In the alcohol group, CXCL8 concentrations were increased in patients with liver and pancreas diseases and there was a significant correlation to aspartate transaminase (r = +0.456, p < 0.001) and gamma-glutamyltransferase (r = +0.647, p < 0.001). Alcohols 7-14 C-X-C motif chemokine ligand 8 Homo sapiens 22-27 28004929-3 2017 The reactivity of solid NaO2 is probed further, and NaF is found to be formed through a reaction between the electrochemically generated NaO2 and the electrode binder, polyvinylidene fluoride (PVDF). NaO2 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 28456799-10 2017 In addition, allicin attenuated the LPS-induced inflammatory responses, including endothelial cell adhesion and TNF-alpha and IL-8 production. allicin 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 28004929-3 2017 The reactivity of solid NaO2 is probed further, and NaF is found to be formed through a reaction between the electrochemically generated NaO2 and the electrode binder, polyvinylidene fluoride (PVDF). polyvinylidene fluoride 168-191 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 28004929-3 2017 The reactivity of solid NaO2 is probed further, and NaF is found to be formed through a reaction between the electrochemically generated NaO2 and the electrode binder, polyvinylidene fluoride (PVDF). polyvinylidene fluoride 193-197 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 27988394-5 2017 UFP-induced IL-8 could be reduced by SB203580, indicating a role of p38MAPK activation in IL-8 production. SB 203580 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 27988394-5 2017 UFP-induced IL-8 could be reduced by SB203580, indicating a role of p38MAPK activation in IL-8 production. SB 203580 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 28849490-7 2017 Treatment with Tau-Ribose significantly modulated the production of IL-8 and IL-6. tau-ribose 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 28977796-9 2017 Under normal flow, SnF/NaF showed higher efficacy, with a significant difference compared to NaF/Sn/Ch, NaF, and placebo (p < 0.05). Tin 19-21 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 28977796-11 2017 Comparing salivary conditions, there were significant differences for SnF/NaF for %SMH after the in situ phase (%SMHtotal)), %RHL and for all toothpastes in case of %RER. N-(2-Ethoxyethyl)-N-{(2s)-2-Hydroxy-3-[(2r)-6-Hydroxy-4-Oxo-3,4-Dihydro-1'h-Spiro[chromene-2,3'-Piperidin]-1'-Yl]propyl}-2,6-Dimethylbenzenesulfonamide 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 28214842-10 2017 The in vitro AGEs generation was also able to be enhanced by the exposure of HaCaT cells to MGO, which reduced dose-dependently cellular viability, damaged mitochondrial function, triggered secretion of interleukin (IL)-6 and IL-8, activated NF-kappaB and upregulated MMP-9 expression. Pyruvaldehyde 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 28002795-0 2017 Sodium fluoride (NaF) causes toxic effects on splenic development in mice. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 28002795-1 2017 At present, very limited studies focus on the toxic effect of sodium fluoride (NaF) on splenic development of human and animals in vivo. Sodium Fluoride 62-77 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 27832944-9 2017 The results indicated that CAPE inhibits LPS-induced IL-6, IL-8, iNOS, and COX-2 production in a dose-dependent manner. caffeic acid phenethyl ester 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 29250545-10 2017 Simvastatin significantly reduced the levels of cTnT, CK-MB, TNF-alpha, IL-6, and IL-8 (P < 0.05), reduced the expression of LC3-II/LC3-I and Beclin 1, and increased the expression of phosphorylation of AMPK. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 28027722-4 2017 Celastrol significantly inhibited poly(I:C)-induced expression of adhesion molecules, such as ICAM-1/VCAM-1, and chemokines, such as CCL2, CXCL8, and CXCL10, in CRT-MG human astroglioma cells. celastrol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 139-144 27846001-5 2017 Although the skeletal uptake of F-NaF was without signs of focal metastasis, the F-NaF PET/CT scanning surprisingly revealed diffuse high accumulation of F-NaF in the lung parenchyma, possibly because of calcium deposition in the lung parenchyma associated to amyloidosis seen in patients with myelomatosis. Calcium 204-211 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 28680337-5 2017 Glutathione treatment decreased the serum levels of asparaginic acid transaminase, alanine aminotransferase, total bilirubin, total bile acids, haluronic acid, collagen IV, laminin, transforming growth factor-beta1, tumour necrosis factor-alpha, interleukin-6, and interleukin-8, compared with the control group. Glutathione 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 265-278 27883241-7 2017 RESULTS: Untreated and IL-8-treated PBNs from the SA group produced higher autophagy and NET levels compared with those from the NSA group (P < 0.01). pbns 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 27883241-7 2017 RESULTS: Untreated and IL-8-treated PBNs from the SA group produced higher autophagy and NET levels compared with those from the NSA group (P < 0.01). sa 50-52 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 27883241-8 2017 IL-8 increased autophagy and NET levels in PBNs from the SA group, but not from the NSA group. pbns 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 27883241-8 2017 IL-8 increased autophagy and NET levels in PBNs from the SA group, but not from the NSA group. sa 57-59 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 28124586-8 2017 RESULTS: High glucose (30.5 mM) increased mRNA expression of interleukin (IL)-6 and secretion of both IL-6 and IL-8 by astrocytes. Glucose 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 29721026-8 2017 Preincubation of ozone at 50 mug/ml decreases IL-8, IL-6, and IL-1beta production by 50, 56, and 70%, respectively, compared to untreated cells. Ozone 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 27573638-11 2017 Follow-up 18F-NaF PET/CT showed persistence of 81.5 % of the baseline 18F-NaF positive MM lesions after treatment, despite the fact that 64.7 % of them had turned to 18F-FDG negative. Fluorine-18 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 27573638-11 2017 Follow-up 18F-NaF PET/CT showed persistence of 81.5 % of the baseline 18F-NaF positive MM lesions after treatment, despite the fact that 64.7 % of them had turned to 18F-FDG negative. Fluorine-18 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 29227717-6 2017 Corticosteroid sensitivity was determined as the dexamethasone concentration causing 40% inhibition of tumor necrosis factor alpha-induced CXCL8 production (Dex-IC40) in the presence or absence of quercetin. Dexamethasone 49-62 C-X-C motif chemokine ligand 8 Homo sapiens 139-144 29256349-5 2017 Notably, analysis of the drug-resistant melanoma cell line selected after prolonged exposure to chemotherapeutic drug dacarbazine revealed higher levels of CXCL8 and CXCR2 compared with parent cells as a signature of drug resistance. Dacarbazine 118-129 C-X-C motif chemokine ligand 8 Homo sapiens 156-161 27865894-7 2017 CYLD induction mediated, at least in part, the TZD-mediated downregulation of tumor necrosis factor alpha (TNFalpha)-induced interleukin 8 (IL-8). tzd 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 125-138 27821648-6 2017 The MAPK and NF-kappaB pathways are involved in both the PKC-mediated and bufalin-promoted PKC regulation of COX-2/IL-8 production. bufalin 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 27821648-10 2017 Bufalin significantly enhances breast cancer xenograft growth, which is accompanied by an elevation in COX-2/IL-8 expression. bufalin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 27821648-5 2017 Using MB-231 breast cancer cells, bufalin augments PKC induction of COX-2/IL-8 at both the protein and mRNA levels, and the production of prostaglandin E2 (PGE2) and IL-8. bufalin 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 27821648-5 2017 Using MB-231 breast cancer cells, bufalin augments PKC induction of COX-2/IL-8 at both the protein and mRNA levels, and the production of prostaglandin E2 (PGE2) and IL-8. bufalin 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 27865894-7 2017 CYLD induction mediated, at least in part, the TZD-mediated downregulation of tumor necrosis factor alpha (TNFalpha)-induced interleukin 8 (IL-8). tzd 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 28751819-7 2017 Tryptase, PAR2 agonists, histamine, and TNF-alpha all enhanced interleukin 8 production by RPE cells, while only tryptase enhanced VEGF production. Histamine 25-34 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 29683134-5 2017 DHA administration resulted in approximately a doubling of plasma and red cell phospholipid and adipose tissue DHA content but no change in systemic markers of inflammation, such as circulating C-reactive protein (CRP) or interleukins (IL) 6, 8 and 10 (IL-6, IL-8, IL-10). Docosahexaenoic Acids 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 29225318-8 2017 Protein microarray analysis showed caffeine suppresses the secretion of inflammatory cytokines, interleukin-8 and plasminogen activator inhibitor-1 from Caco-2 cells. Caffeine 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 96-147 27329245-7 2017 In a study of SASP markers, the expressions of IL6 and IL8 were also more upregulated in human non-pathological prostatic glands after ADT than in untreated specimens. adt 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 27329245-8 2017 IL6, IL8, and MMP2 were expressed more strongly in human prostate cancer specimens resected after ADT than in untreated tumors. adt 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 28163398-0 2017 kappa-Carrageenan Enhances Lipopolysaccharide-Induced Interleukin-8 Secretion by Stimulating the Bcl10-NF-kappaB Pathway in HT-29 Cells and Aggravates C. freundii-Induced Inflammation in Mice. Carrageenan 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 28163398-5 2017 We investigated whether the kappa-carrageenan could enhance lipopolysaccharide-induced IL-8 expression by studying its actions on the TLR4-NF-kappaB pathway. Carrageenan 28-45 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 28163398-8 2017 Our data show that kappa-carrageenan pretreatment promoted LPS-induced IL-8 expression in HT-29 cells. Carrageenan 19-36 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 27878250-2 2017 This study aimed to examine the effects and mechanisms of action of SN38 (a metabolite of the camptothecin derivative, CPT-11) on IL-8 expression in HCT8 cells, using ELISA, CCK-8 and western blot analysis. Camptothecin 94-106 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 27878250-4 2017 Of the other agents, evodiamine was found to inhibit both IL-8 secretion and cell proliferation, and jatrorrhizine was found to increase IL-8 secretion without any obvious inhibitory effect on cell proliferation. evodiamine 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 27878250-4 2017 Of the other agents, evodiamine was found to inhibit both IL-8 secretion and cell proliferation, and jatrorrhizine was found to increase IL-8 secretion without any obvious inhibitory effect on cell proliferation. jatrorrhizine 101-114 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 27878250-7 2017 Thus, the potential benefit of the use of a combination of camptothecin-11 with other chemical drugs with inhibitory effects on IL-8 expression, should be paid more attention in treating colon cancer. Irinotecan 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 27793704-9 2017 RESULTS: For %KHNalt, the polymers alone did not reduce enamel demineralization when compared to the negative control, but Carbopol associated with NaF significantly improved its protective effect. carboxypolymethylene 123-131 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 27793704-11 2017 CONCLUSIONS: It is concluded that Carbopol enhanced NaF"s protection against initial erosion. carboxypolymethylene 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 27903742-11 2017 Our results indicate that the P2Y6/store-operated calcium entry/IL-8 axis is involved in MSU crystal-induced aggregated NET formation, but MRS2578 could have additional effects affecting PMN migration. Calcium 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 27541080-9 2017 Pharmacologic inhibition of AT1R through losartan modulated mRNA transcription of IL-6 and IL-8 in HPLF but not in HGF. Losartan 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 27541080-11 2017 CONCLUSION: These results suggest that AT1R knockdown and AT1R pharmacologic blockade by losartan may differently control balance of inflammatory cytokines, such as IL-6 and IL-8, in primary human periodontal fibroblasts. Losartan 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 29089668-1 2017 The angelicin analogue 4,6,4"-trimethylangelicin (TMA) was recently reported as a strong inhibitor of nuclear factor-kappaB (NF-kappaB) activity and of the expression of the interleukin-8 (IL-8) gene in bronchial epithelial cells in which the inflammatory response has been challenged with P. aeruginosa, the most common bacterium found in the airways of patients affected by cystic fibrosis (CF). angelicin 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 29089668-1 2017 The angelicin analogue 4,6,4"-trimethylangelicin (TMA) was recently reported as a strong inhibitor of nuclear factor-kappaB (NF-kappaB) activity and of the expression of the interleukin-8 (IL-8) gene in bronchial epithelial cells in which the inflammatory response has been challenged with P. aeruginosa, the most common bacterium found in the airways of patients affected by cystic fibrosis (CF). 4,4',6-trimethylangelicin 23-48 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 29089668-1 2017 The angelicin analogue 4,6,4"-trimethylangelicin (TMA) was recently reported as a strong inhibitor of nuclear factor-kappaB (NF-kappaB) activity and of the expression of the interleukin-8 (IL-8) gene in bronchial epithelial cells in which the inflammatory response has been challenged with P. aeruginosa, the most common bacterium found in the airways of patients affected by cystic fibrosis (CF). 4,4',6-trimethylangelicin 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 28592115-3 2017 Among the inflammation-associated cytokines assayed, high level of chemokines CXCL8/IL-8 (6.82-fold increase) and CXCL10/IP-10 (16.45-fold increase) in TCS than that in paired NCS were evidently identified. 9-ethyl-N-(3,4,5-trimethoxyphenyl)carbazole-3-sulfonamide 152-155 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 28592115-3 2017 Among the inflammation-associated cytokines assayed, high level of chemokines CXCL8/IL-8 (6.82-fold increase) and CXCL10/IP-10 (16.45-fold increase) in TCS than that in paired NCS were evidently identified. 9-ethyl-N-(3,4,5-trimethoxyphenyl)carbazole-3-sulfonamide 152-155 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 29558759-7 2017 RESULTS: Treatment with antipsychotic drugs plus vitamin B12 led to a decreased expression of IL-8 and TNF-alpha and an increased expression of TGF-beta. Vitamin B 12 49-60 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 29514151-13 2017 Dopamine significantly increased IL-8 production in human macrophages, an effect that was partially reduced by propranolol. Dopamine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 27819395-3 2017 Here, we describe the mechanisms through which TCA affects human astrocytes, demonstrating: a late apoptotic process, mediated by caspases 9 and 3 activation, involving the Bcl2-Bak-axis; an early and late p38 MAPK activation; an interference with the IL-8 and MCP-1 secretory response. Trichloroacetic Acid 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 29514151-13 2017 Dopamine significantly increased IL-8 production in human macrophages, an effect that was partially reduced by propranolol. Propranolol 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 29558759-5 2017 Thus, the main aim of this clinical trial study was to determine the effects of treatment with risperidone and quetiapine, as antipsychotic drugs, with and without vitamin B12 on the psychotic symptoms of AD patients and the expression of IL-6, IL-8, tumor growth factor (TGF)-beta, tumor necrosis factor (TNF)-alpha, and endothelin (ET)-1). Risperidone 95-106 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 27813716-9 2017 PGF around nonirradiated mini-implants showed higher levels of IL-8. Prostaglandins F 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 28831459-9 2017 CONCLUSION: The AmF/NaF/SnCl2 solution proved to be effective in reducing dental enamel surface loss and its use twice a day potentiated its anti-erosive effect. stannous chloride 24-29 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 29147073-0 2017 Metformin Suppressed CXCL8 Expression and Cell Migration in HEK293/TLR4 Cell Line. Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 21-26 29147073-5 2017 This study intended to address the role of metformin in regulation of CXCL8 expression and cell proliferation and migration. Metformin 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 70-75 29147073-6 2017 Our data indicated that metformin suppressed LPS-induced CXCL8 expression in a dose-dependent manner through inhibiting NF-kappaB, but not AP-1 and C/EBP, activities under the conditions we used. Metformin 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 57-62 28804534-6 2017 In addition, when infected by prominent periodontal pathogens, Porphyromonas gingivalis (ATCC 33277), rapamycin-pretreated groups decreased the expression of inflammatory cytokines (IL-6 and IL-8) compared with the control group. Sirolimus 102-111 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 28088291-5 2017 Both anteiso- and iso- BCFA reduce IL-8. anteiso- and iso- bcfa 5-27 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 28088291-0 2017 BCFA suppresses LPS induced IL-8 mRNA expression in human intestinal epithelial cells. bcfa 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 28088291-6 2017 Anteiso-BCFA more effectively suppressed IL-8 than iso-BCFA in LPS stimulated Caco-2 cells. anteiso-bcfa 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 28462713-11 2017 Full length PMAP-23 induced IL-8 production in porcine epithelial cells, however, this activity was lost in all truncated peptides. pmap 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 28088291-6 2017 Anteiso-BCFA more effectively suppressed IL-8 than iso-BCFA in LPS stimulated Caco-2 cells. bcfa 8-12 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 27411707-7 2016 Interestingly, although very high concentrations (25-50 microM) of Simvastatin resulted in dramatically less IL-6 and IL-8 pro-inflammatory cytokine secretion, 2.5 microM Simvastatin did not reduce the total amount of pro-inflammatory cytokines secreted during mechanical stimulation. Simvastatin 67-78 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 27989874-9 2016 RESULTS: Ingestion of DT suppressed CD4+ T cell expression of IL-1beta and Il-8 (p<0.05) and up-regulated the expression of IL-10 and the Treg/IL-17 ratio (p<0.05) which was not shown in PL. Thymidine 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 28039491-0 2016 Sodium fluoride (NaF) induces the splenic apoptosis via endoplasmic reticulum (ER) stress pathway in vivo and in vitro. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 28039491-2 2016 Therefore, the aim of this study was to define sodium fluoride (NaF)-induced apoptosis mediated by ER stress in the spleen of mice in vivo and in vitro. Sodium Fluoride 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 27935985-0 2016 miR-125b Enhances IL-8 Production in Early-Onset Severe Preeclampsia by Targeting Sphingosine-1-Phosphate Lyase 1. mir-125b 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 27935985-5 2016 We also found that miR-125b enhanced IL-8 production by directly targeting sphingosine-1-phosphate lyase 1 (SGPL1), and this effect could be reversed by SGPL1 overexpression. mir-125b 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 27935985-7 2016 Our data demonstrated a critical role of miR-125b in IL-8 production and the development of PE. mir-125b 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 27789120-8 2016 Curcumin was found to exert diverse immunomodulatory effects, including suppression of IL-4, IL-8, and tumor necrosis factor alpha and increased production of IL-10 and soluble intercellular adhesion molecule. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 27489081-0 2016 Activation of liver X receptor attenuates lysophosphatidylcholine-induced IL-8 expression in endothelial cells via the NF-kappaB pathway and SUMOylation. Lysophosphatidylcholines 42-65 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 27810785-0 2016 Gallic acid reduces cell growth by induction of apoptosis and reduction of IL-8 in HepG2 cells. Gallic Acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 27567939-5 2016 RESULTS: The glucose median value was 4.72mmol/L in SST tubes, 4.67mmol/L in lithium-heparin and 4.44mmol/L in NaF-KOx tubes. Glucose 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 26303504-5 2016 The water-soluble and insoluble fractions of PM2.5 suspension were both shown to induce IL-8 expression. Water 4-9 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 26303504-8 2016 Employment of the transition metal chelators including TPEN (N,N,N",N"-tetrakis (2-pyridylmethyl) ethylenediamine) or DFO (desferrioxamine) inhibited IL-8 expression induced by PM2.5 by over 20% in BEAS-2B cells, but had minimal effect in THP-1 cells. Metals 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 26303504-8 2016 Employment of the transition metal chelators including TPEN (N,N,N",N"-tetrakis (2-pyridylmethyl) ethylenediamine) or DFO (desferrioxamine) inhibited IL-8 expression induced by PM2.5 by over 20% in BEAS-2B cells, but had minimal effect in THP-1 cells. N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 26303504-8 2016 Employment of the transition metal chelators including TPEN (N,N,N",N"-tetrakis (2-pyridylmethyl) ethylenediamine) or DFO (desferrioxamine) inhibited IL-8 expression induced by PM2.5 by over 20% in BEAS-2B cells, but had minimal effect in THP-1 cells. Deferoxamine 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 26303504-8 2016 Employment of the transition metal chelators including TPEN (N,N,N",N"-tetrakis (2-pyridylmethyl) ethylenediamine) or DFO (desferrioxamine) inhibited IL-8 expression induced by PM2.5 by over 20% in BEAS-2B cells, but had minimal effect in THP-1 cells. Deferoxamine 123-138 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 27553225-4 2016 Palmitate inhibited IGFBP-3 secretion by THP-1 macrophages and enhanced IL-8 expression. Palmitates 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 27553225-5 2016 Exposure of palmitate-treated THP-1 macrophages to IGFBP-3-deficient conditioned medium led to a 20-fold increase in palmitate-induced IL-8 expression by hepatocytes. Palmitates 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 27553225-5 2016 Exposure of palmitate-treated THP-1 macrophages to IGFBP-3-deficient conditioned medium led to a 20-fold increase in palmitate-induced IL-8 expression by hepatocytes. Palmitates 117-126 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 27553225-6 2016 Conversely, overexpression of IGFBP-3 suppressed JNK and NF-kappaB activation and blocked palmitate-induced IL-8 expression in hepatocytes. Palmitates 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 27553225-7 2016 Silencing IGFBP-3 in Huh7 cells enhanced JNK and NF-kappaB activity and increased palmitate-induced IL-8 secretion. Palmitates 82-91 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 27553225-9 2016 Under lipotoxic conditions, palmitate inhibits hepatic macrophage secretion of IGFBP-3, thereby releasing the brake and enhancing palmitate-induced IL-8 synthesis and secretion.-Min, H.-K., Maruyama, H., Jang, B. K., Shimada, M., Mirshahi, F., Ren, S., Oh, Y., Puri, P., Sanyal, A. J. Suppression of IGF binding protein-3 by palmitate promotes hepatic inflammatory responses. Palmitates 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 27553225-9 2016 Under lipotoxic conditions, palmitate inhibits hepatic macrophage secretion of IGFBP-3, thereby releasing the brake and enhancing palmitate-induced IL-8 synthesis and secretion.-Min, H.-K., Maruyama, H., Jang, B. K., Shimada, M., Mirshahi, F., Ren, S., Oh, Y., Puri, P., Sanyal, A. J. Suppression of IGF binding protein-3 by palmitate promotes hepatic inflammatory responses. Palmitates 130-139 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 27553225-9 2016 Under lipotoxic conditions, palmitate inhibits hepatic macrophage secretion of IGFBP-3, thereby releasing the brake and enhancing palmitate-induced IL-8 synthesis and secretion.-Min, H.-K., Maruyama, H., Jang, B. K., Shimada, M., Mirshahi, F., Ren, S., Oh, Y., Puri, P., Sanyal, A. J. Suppression of IGF binding protein-3 by palmitate promotes hepatic inflammatory responses. Palmitates 130-139 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 27680872-9 2016 Furthermore, the expression of IL-6 and IL-8 increased in LPA-stimulated human primary granulosa cells (P < .01). lysophosphatidic acid 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 27680872-10 2016 Co-stimulation with rPEDF decreased the expression of LPA-induced IL-6 and IL-8 mRNA and protein by 4- and 2- to 5-fold, respectively. lysophosphatidic acid 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 28164553-2 2016 The emergence of DTC may be affected by various predisposing genetic alterations and environmental factors The aim of this study was to investigate the role of VEGF C936T and IL-8 A251T gene polymorphisms in the pathogenesis and metastasis of differentiated thyroid cancer. dtc 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 28164553-11 2016 The frequency of IL-8 TT was higher in the DTC group with lymph gland metastasis (TT 92%) than in the group without lymph gland metastasis (TT 45.9%) (p < 0.05). dtc 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 28164553-12 2016 CONCLUSIONS: We consider that the VEGF 936 TT genotype may play a protective role in the development of DTC and that the IL-8 A-251 TT genotype may contribute to the DTC lymph node metastasis. dtc 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 27444747-13 2016 Conversely, sex-hormone binding globulin, abdominal visceral fat, interleukin-8, adiponectin were stronger correlates of triglycerides; abdominal visceral fat, and testosterone of high-density lipoprotein cholesterol; and age of both non high-density lipoprotein and low-density lipoprotein in postmenopausal than premenopausal women. Triglycerides 121-134 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 28391662-2 2016 This study aimed to determine whether a dentifrice containing 5% CSPS and fluoride as sodium fluoride (NaF; "Test dentifrice") was non-inferior to a dentifrice containing 5% CSPS and fluoride as sodium monofluorophosphate (SMFP; "Comparator dentifrice") in reducing DH after eight weeks" twice-daily brushing. Fluorides 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 28391662-2 2016 This study aimed to determine whether a dentifrice containing 5% CSPS and fluoride as sodium fluoride (NaF; "Test dentifrice") was non-inferior to a dentifrice containing 5% CSPS and fluoride as sodium monofluorophosphate (SMFP; "Comparator dentifrice") in reducing DH after eight weeks" twice-daily brushing. Sodium Fluoride 86-101 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 27489081-4 2016 The LXR agonist significantly inhibited lysophosphatidylcholine (LPC)-induced IL-8 production in a dose-dependent manner without appreciable cytotoxicity. Lysophosphatidylcholines 40-63 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 27489081-4 2016 The LXR agonist significantly inhibited lysophosphatidylcholine (LPC)-induced IL-8 production in a dose-dependent manner without appreciable cytotoxicity. Lysophosphatidylcholines 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 27445292-17 2016 18F-NaF PET demonstrates repeatability levels useful for clinically quantifying the response of bone lesions to therapy. Fluorine-18 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 28066685-6 2016 Linoleic acid also significantly increased IL-6 by 2.9-fold and IL-8 by 5.7-fold. Linoleic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 28066685-8 2016 Linoleic acid increased IL-8 concentrations by 56% in human RMEC conditioned medium. Linoleic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 27779898-7 2016 The active form of VD is 1,25(OH)2D3 that produces biological effects via the nuclear hormone receptor named VD receptor (VDR), which may interfere with the immune cells and macrophages leading to the suppression of the inflammatory process by decreasing the release of TNF-alpha, IL-1, IL-6, and IL-8, IL-12, and IL-23. Calcitriol 25-36 C-X-C motif chemokine ligand 8 Homo sapiens 297-301 27634981-1 2016 We describe the role of 18F-sodium fluoride (18F-NaF) PET/CT bone scanning in the staging of breast and prostate cancer. 18f-sodium fluoride 24-43 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 28039406-13 2016 Polyphenol supplementation may attenuate the IL-8 response, however, did not affect granulocyte percentage and adhesion molecule expression in peripheral blood following resistance exercise. Polyphenols 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 27906095-0 2016 Resveratrol and acetyl-resveratrol modulate activity of VEGF and IL-8 in ovarian cancer cell aggregates via attenuation of the NF-kappaB protein. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 27906095-0 2016 Resveratrol and acetyl-resveratrol modulate activity of VEGF and IL-8 in ovarian cancer cell aggregates via attenuation of the NF-kappaB protein. acetyl-resveratrol 16-34 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 27416953-5 2016 Then, cells were kept in contact with inflammatory cytokines (TNF-alpha, IL-1beta, IL-6, and IL-8) in serum-free DMEM for 24 hours. dmem 113-117 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 27090657-3 2016 Monomer 2,7-(2-hydroxy-3-methacryloyloxypropoxy)naphthalene (2,7-NAF.DM) with luminophoric properties was immobilized on silica and carbon nanotubes in two ways: mechanical mixing with previously obtained polymer and by in situ oligomerization with chemisorption after carrier"s modification with vinyl groups. HNPM 8-59 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 27090657-3 2016 Monomer 2,7-(2-hydroxy-3-methacryloyloxypropoxy)naphthalene (2,7-NAF.DM) with luminophoric properties was immobilized on silica and carbon nanotubes in two ways: mechanical mixing with previously obtained polymer and by in situ oligomerization with chemisorption after carrier"s modification with vinyl groups. dm 69-71 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 27090657-3 2016 Monomer 2,7-(2-hydroxy-3-methacryloyloxypropoxy)naphthalene (2,7-NAF.DM) with luminophoric properties was immobilized on silica and carbon nanotubes in two ways: mechanical mixing with previously obtained polymer and by in situ oligomerization with chemisorption after carrier"s modification with vinyl groups. Silicon Dioxide 121-127 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 27782292-5 2016 DMA significantly attenuated the secretion of TNFalpha, IL-6, IL-10, and granulocyte macrophage colony stimulating factor (GM-CSF) from LPS-stimulated RAW 264.7 cells, IL-6 secretion from TNFalpha-stimulated JEG-3 cells and TNFalpha, IL-6, IL-10, GM-CSF and Interleukin-8 (IL-8) from LPS-stimulated human placental explants. dimethylacetamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 258-271 27782292-5 2016 DMA significantly attenuated the secretion of TNFalpha, IL-6, IL-10, and granulocyte macrophage colony stimulating factor (GM-CSF) from LPS-stimulated RAW 264.7 cells, IL-6 secretion from TNFalpha-stimulated JEG-3 cells and TNFalpha, IL-6, IL-10, GM-CSF and Interleukin-8 (IL-8) from LPS-stimulated human placental explants. dimethylacetamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 273-277 27889107-6 2016 However, supplementing adipocytes with an equal combination of malvidin plus peonidin followed by LPS treatment decreased the mRNA levels of interleukin (IL)-6, IL-1beta, IL-8, monocyte chemoattractant protein-1, toll-like receptor-2, tumor necrosis factor alpha, cyclooxygenase-2, and interferon gamma-induced protein-10. peonidin 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 27558640-4 2016 In vitro, treatment with ramalin produced significantly less inflammatory chemokines and cytokines, including TARC, MCP-1, RANTES, and IL-8 in TNF-alpha-stimulated HaCaT cells. Ramalin 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 27892491-9 2016 IL-1alpha and IL-8, HSPA1A and FOSL1 were significantly upregulated following 24-h treatment with CuCl2 and Cu(OAc)2 at 58 and 580 muM without concomitant inhibition in cell viability. cupric chloride 98-103 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 27349353-8 2016 The anti-inflammatory potency of DXM-loaded CMS (10-E-15-350) nanocarriers was assessed in TNFalpha supplemented skin models, where a significant reduction of the pro-inflammatory cytokine IL-8 was seen, with markedly greater efficacy than commercial DXM cream. Dexamethasone 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 27886000-15 2016 CONCLUSIONS: In this study, micro layered esthetic nickel titanium wires are found biocompatible among other wires and NaF and CHX mouthwashes can be recommend for their good corrosion resistance during fixed orthodontic therapy. Nickel 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 119-122 27892491-9 2016 IL-1alpha and IL-8, HSPA1A and FOSL1 were significantly upregulated following 24-h treatment with CuCl2 and Cu(OAc)2 at 58 and 580 muM without concomitant inhibition in cell viability. cupric acetate 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 27874084-6 2016 Moreover, silymarin attenuated CSE-induced upregulation of inflammatory cytokines TNF-alpha, IL-6 and IL-8 which could also be dampened by ERK/p38 MAPK inhibitors and siRNAs for Beclin-1 and Atg5. Silymarin 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 27933092-6 2016 The decrease in the CXCL8 level was negatively correlated with the increase in the how-density lipoprotein-cholesterol (HDL-C) level and was positively correlated with the decrease in the soluble P-selectin (sP-selectin) level in the anthocyanin group. Cholesterol 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 20-25 27933092-6 2016 The decrease in the CXCL8 level was negatively correlated with the increase in the how-density lipoprotein-cholesterol (HDL-C) level and was positively correlated with the decrease in the soluble P-selectin (sP-selectin) level in the anthocyanin group. TFF2 protein, human 208-210 C-X-C motif chemokine ligand 8 Homo sapiens 20-25 27933092-6 2016 The decrease in the CXCL8 level was negatively correlated with the increase in the how-density lipoprotein-cholesterol (HDL-C) level and was positively correlated with the decrease in the soluble P-selectin (sP-selectin) level in the anthocyanin group. Anthocyanins 234-245 C-X-C motif chemokine ligand 8 Homo sapiens 20-25 27835611-4 2016 We also studied the role of TLR4 in Co2+-mediated adhesion molecule expression in MonoMac 6 macrophages.We show that Co2+ increases secretion of inflammatory cytokines, including IL-6 and IL-8, in HMEC-1. Cobalt(2+) 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 27956797-13 2016 We also showed that subjects with CD seem to have a lowered production of IL8 in response to MDP in the presence of LB. lb 116-118 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 27849035-8 2016 Sodium iodate also increased expression of FGF-2, but suppressed expression of IL-8, PDGF, TIMP-2 and VEGF. sodium iodate 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 27869178-9 2016 We conclude that interactions of nickel ions with histidine residues in domain B help to maintain the conformation of the C-terminal region to conserve the integrity of the HpGroES structure and modulate IL-8 release. Nickel 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 27869178-9 2016 We conclude that interactions of nickel ions with histidine residues in domain B help to maintain the conformation of the C-terminal region to conserve the integrity of the HpGroES structure and modulate IL-8 release. Histidine 50-59 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 27575568-6 2016 As a result from the inflammatory response, IPOH [50muM] induced an increase of both IL-6 and IL-8 secretion in A549 (1.5-fold change) and in 16HBE14o- (2.8- and 7-fold change respectively). ipoh 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 27575568-7 2016 4-OPA [50muM] treatment of A549 increased IL-6 (1.4-times) and IL-8 (1.3-times) levels, while in 16HBE14o- had an opposite effect. 4-oxopentanal 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 27575568-8 2016 A549 treated with 4-AMCH [50muM] elevate both IL-6 and IL-8 levels by 1.2-times, while in 16HBE14o- had an opposite effect. 4-acetyl-1-methylcyclohexene 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 27740938-0 2016 7-Ketocholesterol induces ATM/ATR, Chk1/Chk2, PI3K/Akt signalings, cytotoxicity and IL-8 production in endothelial cells. 7-ketocholesterol 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 27852250-11 2016 Greater inhibition of IL-8 production was observed in neutrophils from patients with SS asthma treated with DEX/atopic asthmatic serum combination compared with SR asthma patients, though DEX alone showed the same effect on neutrophils from SS and SR asthma patients. Dexamethasone 108-111 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 27904665-11 2016 (3) ELISA showed IL-8 in the supernatant increased significantly in a time dependent manner after HCY treatment (P<0.01), but curcumin could significantly inhibit the IL-8 secretion in endothelial cells after HCY treatment. Homocysteine 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 27904665-11 2016 (3) ELISA showed IL-8 in the supernatant increased significantly in a time dependent manner after HCY treatment (P<0.01), but curcumin could significantly inhibit the IL-8 secretion in endothelial cells after HCY treatment. Curcumin 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 27904665-13 2016 CONCLUSION: Curcumin is able to protect the endothelial cells against HCY induced injury through inhibiting NF-kappaB activation and down-regulating IL-8 expression. Curcumin 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 27849062-4 2016 Herein, we show that FTY720-P enhances TNF-induced PP2A phosphatase activity and significantly represses TNF-induced interleukin 6 (IL-6) and IL-8 mRNA expression and protein secretion from A549 lung epithelial cells. FTY 720P 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 27740938-10 2016 LY294002 attenuated the 7-KC-induced apoptosis and IL-8 mRNA expression of endothelial cells. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 27713966-0 2016 Hydroxysafflor yellow A inhibits IL-1beta-induced release of IL-6, IL-8, and MMP-1 via suppression of ERK, NF-kappaB and AP-1 signaling in SW982 human synovial cells. hydroxysafflor yellow A 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 27877060-6 2016 RESULTS: In a keratinocyte model, ES0 inhibited the expression of the inflammatory mediators, thymic stromal lymphopoietin, interleukin (IL)-18, IL-4R, IL-8, monocyte chemoattractant protein-3, macrophage inflammatory protein-3alpha, and macrophage-derived chemokine and induced the expression of involucrin, which is involved in skin barrier keratinocyte terminal differentiation. 2-amino-1H-Benzimidazol-7-ol 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 27713966-7 2016 These results indicate that the inhibitory effects of HSYA on IL-1beta-induced IL-6, IL-8 and MMP-1 release might be mediated via suppression of ERK, nuclear factor-kappaB (NF-kappaB) and activator protein-1 (AP-1) signaling pathways. hydroxysafflor yellow A 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 27398628-4 2016 One of these is based on the use of the old sulfone antibiotic dapsone that has demonstrated several interleukin-8 system inhibiting actions. Sulfones 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 101-114 27753495-3 2016 We found the transition concentration is ion-specific, and the capacity of sodium halide salts to inhibit bubble coalescence follows the order of NaF > NaCl > NaBr > NaI. sodium halide salts 75-94 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 27753495-3 2016 We found the transition concentration is ion-specific, and the capacity of sodium halide salts to inhibit bubble coalescence follows the order of NaF > NaCl > NaBr > NaI. Sodium Chloride 155-159 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 27753495-3 2016 We found the transition concentration is ion-specific, and the capacity of sodium halide salts to inhibit bubble coalescence follows the order of NaF > NaCl > NaBr > NaI. sodium bromide 165-169 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 27753495-3 2016 We found the transition concentration is ion-specific, and the capacity of sodium halide salts to inhibit bubble coalescence follows the order of NaF > NaCl > NaBr > NaI. Sodium Iodide 175-178 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 27281349-5 2016 Budesonide suppressed secreted chemokines IL-8 and CCL2 (MCP-1) within 4 hours, reaching a 90% decrease at 12 hours, which was fully reversed 72 hours after removal of the steroid. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 27890374-6 2016 The serum concentrations of IL-8 from MASP group and SAP group obviously increased at day 1, and there was significant difference between MASP group and MAP group, SAP group and MSAP group (P < 0.05), while the difference between MAP group and control group was not obvious (P > 0.05); The serum concentrations of MCP-1, TNF-alpha and IL-8 from MAP group all reached the highest level at day 4, which were significantly higher than the detection levels at day 1. msap 178-182 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 27890374-7 2016 In MSAP group and SAP group, the serum concentrations of MCP-1, TNF-alpha and IL-8 were the highest at day 1, which were significantly higher than the detection levels at day 4 and 7. msap 3-7 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 27890374-8 2016 At each detecting timing, the serum concentrations of MCP-1, TNF-alpha and IL-8 from MSAP group and SAP group were all higher than those of MAP group and MSAP group, respectively. msap 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 26147617-9 2016 In the symptomatic group, the mean 18F-NaF TBR was 2 12 +- 0 44, and in the asymptomatic group, it was 1 85 +- 0 46. tbr 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 26147617-10 2016 The 18F-NaF/18F-FDG showed that, overall, 18F-NaF uptake is higher than 18F-FDG. Fluorodeoxyglucose F18 12-19 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 26147617-10 2016 The 18F-NaF/18F-FDG showed that, overall, 18F-NaF uptake is higher than 18F-FDG. Fluorodeoxyglucose F18 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 26147617-11 2016 In the symptomatic plaques, the 18F-NaF was higher for the low calcium content and the lowest for the high. Calcium 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 27655676-4 2016 Using an under agarose chemotaxis assay, we observed that the bacterial fMLP-induced neutrophil chemotaxis signal overrode interleukin 8 (IL-8)- and leukotriene B4 (LTB4)-induced chemotaxis signals. Sepharose 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 123-136 27655676-4 2016 Using an under agarose chemotaxis assay, we observed that the bacterial fMLP-induced neutrophil chemotaxis signal overrode interleukin 8 (IL-8)- and leukotriene B4 (LTB4)-induced chemotaxis signals. Sepharose 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 27591243-13 2016 14,15-EET treatment resulted in a significant reduction in IL-6, IL-8, and MCP-1 secretion, and increased accumulation of Nrf2 and expression of HO-1. 14,15-epoxy-5,8,11-eicosatrienoic acid 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 27890374-9 2016 CONCLUSIONS: The dynamic changes of serum levels of MCP-1, TNF-alpha and IL-8 in patients with acute pancreatitis have their rules, and the change rule of MAP group was different with that of MSAP and SAP group, which showed the reference value for the diagnosis and illness severity evaluation of acute pancreatitis. msap 192-196 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 27398628-4 2016 One of these is based on the use of the old sulfone antibiotic dapsone that has demonstrated several interleukin-8 system inhibiting actions. Dapsone 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 101-114 27398628-5 2016 Erlotinib typically gives a rash that has recently been proven to come out via up-regulated keratinocyte interleukin-8 synthesis with histological features reminiscent of typical neutrophilic dermatoses. Erlotinib Hydrochloride 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 27398628-6 2016 In this review, we report experimental evidence that shows the use of dapsone to improve quality of life in erlotinib-treated patients by ameliorating rash as well as short-circuiting a growth-enhancing aspect of erlotinib based on increased interleukin-8 secretion. Dapsone 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 242-255 27398628-6 2016 In this review, we report experimental evidence that shows the use of dapsone to improve quality of life in erlotinib-treated patients by ameliorating rash as well as short-circuiting a growth-enhancing aspect of erlotinib based on increased interleukin-8 secretion. Erlotinib Hydrochloride 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 242-255 27882140-11 2016 Thus, HES 130/0.4 resuscitation could decrease the IL-1 and IL-8 levels, shorten the duration of positive FB, and preserve the patient"s immune status as well as renal function during the early phase of SAP. Hydroxyethyl Starch Derivatives 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 27404512-7 2016 Using an ELISArray approach for the simultaneous detection of several analytes (cytokines/chemokines), it was found that only ZnO and AgNP20 increased the production of different analytes including the potent pro-inflammatory CXCL8 (IL-8) chemokine. Zinc Oxide 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 226-231 27598863-9 2016 Pearson correlation exhibited a relationship between the ABTS assay and the expression of three out of five analyzed genes; IL-1beta, IL-6 and IL-8. 2,2'-azino-di-(3-ethylbenzothiazoline)-6-sulfonic acid 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 27012464-9 2016 MPAID also inhibited TNF-alpha-induced NF-kappaB transcriptional activity, the mRNA expression of IL-6 and IL-8, and IL-6 production. mpaid 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 26744271-0 2016 Elevated mRNA expression of PGF2alpha receptor splice variant 2(FP-V2) in human decidua is associated with incomplete mifepristone-misoprostol-induced early medical abortion by regulation of interleukin-8. Misoprostol 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 191-204 27404512-7 2016 Using an ELISArray approach for the simultaneous detection of several analytes (cytokines/chemokines), it was found that only ZnO and AgNP20 increased the production of different analytes including the potent pro-inflammatory CXCL8 (IL-8) chemokine. Zinc Oxide 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 27542947-17 2016 However, the secretion patterns of hIGF1 and IL8 differed in the luteal phase when comparing steroid treatment with follicle co-culture. Steroids 93-100 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 27538572-4 2016 In primary human cell cultures, we found that hepta-1855 functioned as a potent TLR4 agonist by priming neutrophil respiratory burst and stimulating strong IL-8 from monocytes and neutrophils. hepta-1855 46-56 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 27538572-8 2016 We found that penta-1447 lacked immunostimulatory activity but interfered with inflammatory IL-8 synthesis in response to hexa-1685. PENTA 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 27538572-9 2016 Together, these observations suggest a potential contribution of hepta-1855 to maintenance of the inflammatory burden in late-stage CF by recruiting neutrophils via IL-8 and promoting their survival, an effect presumably amplified by the absence of penta-1447. hepta-1855 65-75 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 26558835-5 2016 The long-distance sculling intensity variables such as the average rating of perceived exertion, HR and blood lactate were correlated with changes in IL-8, IL-1alpha and IL-1beta levels (r=0.47 to r=0.59; P<0.05). Lactic Acid 110-117 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 27861337-9 2016 The changes in IL-8 also differed significantly between LDV/SOF + RBV and LDV/SOF groups (P < 0.05). Ribavirin 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 27345703-9 2016 Interleukin-8 (IL-8) release was increased by all particulates, avobenzone, homosalate and octylsalicylate. avobenzone 64-74 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 27345703-9 2016 Interleukin-8 (IL-8) release was increased by all particulates, avobenzone, homosalate and octylsalicylate. avobenzone 64-74 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 27345703-9 2016 Interleukin-8 (IL-8) release was increased by all particulates, avobenzone, homosalate and octylsalicylate. homosalate and octylsalicylate 76-106 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 27345703-9 2016 Interleukin-8 (IL-8) release was increased by all particulates, avobenzone, homosalate and octylsalicylate. homosalate and octylsalicylate 76-106 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 27542947-19 2016 In co-culture, IL8 secretion was also suppressed on luteal phase day 15 (P = 0.013) versus follicular phase day 7, but IL8 secretion increased continuously under high E2/progesterone treatment (P = 0.003 for D13 versus D3). Progesterone 170-182 C-X-C motif chemokine ligand 8 Homo sapiens 119-122 27287090-13 2016 Lysed neutrophils inhibited RV16-induced IL-6 and CXCL8 from monocytes. rv16 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 27490714-7 2016 RESULTS: Following intramuscular capsaicin injection, pro-inflammatory cytokines [TNFalpha, IL-6, IL-8] significantly increased (percent rise from baseline) in both groups, whereas IL-1beta significantly increased in the PTSD group only. Capsaicin 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 27494070-8 2016 In vitro, dexamethasone reduced the IL-8-mediated release of MMP-9 from neutrophils, indicating that glucocorticoids may exert rapid effects on neutrophil activation. Dexamethasone 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 27287090-14 2016 Neutrophil intracellular components alone effectively inhibited RV16-induced monocyte-derived IL-6 and CXCL8. rv16 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 103-108 27287090-15 2016 Neutrophil intracellular components reduced RV16-induced IL-6 and CXCL8 mRNA in monocytes. rv16 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 66-71 27770804-9 2016 Dust extract induction of IL-8 gene expression was associated with increased DHE-fluorescence and 4-HNE staining, and antioxidants suppressed inflammatory gene induction. dihydroethidium 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 27852393-5 2016 Results: The mRNA levels of Acanthamoeba-induced TLR4, MyD88, NF-kappaB, TNF-alpha, IFN-beta and IL-8 in THCEs under hypoxia was down-regulated by 47%, 41%, 45%, 53%, 36% and 50% respectively, compared to control group. thces 105-110 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 27791031-6 2016 IL-8 knockdown inhibits tamoxifen-resistant cell growth and invasion and partially attenuates the effect of overexpressed FOXA1. Tamoxifen 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 27776166-7 2016 Furthermore, GlcN suppressed the expression of proinflammatory cytokine genes (such as IL-6, IL-8, IL-24 and TNF-alpha genes). Glucosamine 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 27664576-9 2016 The metabolites of CTH and CBS, l-cystathionine and l-cysteine, attenuated the formaldehyde-induced upregulation of pro-inflammatory DEGs, MMP1, PTGS2, and CXCL8, suggesting that CTH and CBS play a role in the negative feedback regulation of formaldehyde-induced pro-inflammatory responses in NHKs. Cystathionine 32-47 C-X-C motif chemokine ligand 8 Homo sapiens 156-161 27664576-9 2016 The metabolites of CTH and CBS, l-cystathionine and l-cysteine, attenuated the formaldehyde-induced upregulation of pro-inflammatory DEGs, MMP1, PTGS2, and CXCL8, suggesting that CTH and CBS play a role in the negative feedback regulation of formaldehyde-induced pro-inflammatory responses in NHKs. Cysteine 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 156-161 27664576-9 2016 The metabolites of CTH and CBS, l-cystathionine and l-cysteine, attenuated the formaldehyde-induced upregulation of pro-inflammatory DEGs, MMP1, PTGS2, and CXCL8, suggesting that CTH and CBS play a role in the negative feedback regulation of formaldehyde-induced pro-inflammatory responses in NHKs. Formaldehyde 79-91 C-X-C motif chemokine ligand 8 Homo sapiens 156-161 27768727-8 2016 In patients with a history of peritonitis (5 of 20), AlaGln supplementation decreased dialysate interleukin-8 levels. alanylglutamine 53-59 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 27776166-8 2016 In addition, GlcN-mediated O-GlcNAc modification was involved in the downregulation of TNF-alpha and IL-8 genes but not IL-6 and IL-24 genes, based on the effects of alloxan, an O-GlcNAc transferase inhibitor. Glucosamine 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 27776166-8 2016 In addition, GlcN-mediated O-GlcNAc modification was involved in the downregulation of TNF-alpha and IL-8 genes but not IL-6 and IL-24 genes, based on the effects of alloxan, an O-GlcNAc transferase inhibitor. o-glcnac 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 27980779-8 2016 Conversely, several immunological effects of ProMune like IL-8 secretion are independent of CG-motifs and could be ascribed to the phosphorothioate-modifications of its DNA backbone, which may have caused the side effects of ProMune in clinical trials. Parathion 132-148 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 27799756-5 2016 OBJECTIVE: The objective of the study was to test whether the daily inhalation of the registered ectoine-containing medical device (Ectoin inhalation solution) leads to a reduction of neutrophilic cells and interleukin-8 (IL-8) levels in the sputum of persons with mild symptoms of airway disease due to lifelong exposure to environmental air pollution. ectoine 97-104 C-X-C motif chemokine ligand 8 Homo sapiens 208-221 27799756-5 2016 OBJECTIVE: The objective of the study was to test whether the daily inhalation of the registered ectoine-containing medical device (Ectoin inhalation solution) leads to a reduction of neutrophilic cells and interleukin-8 (IL-8) levels in the sputum of persons with mild symptoms of airway disease due to lifelong exposure to environmental air pollution. ectoine 97-104 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 27700067-3 2016 The best estimates of the Gibbs free energies characterizing the AlF4- and NaF2- fragmentation reactions in a water solvent are evaluated as equal to 33-34 and 12-14 kcal/mol, respectively (assuming the F- and AlF3/NaF products) or 14-15 and 26-28 kcal/mol, respectively (assuming the HF and AlF3OH-/NaFOH- products). Water 110-115 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 27700067-3 2016 The best estimates of the Gibbs free energies characterizing the AlF4- and NaF2- fragmentation reactions in a water solvent are evaluated as equal to 33-34 and 12-14 kcal/mol, respectively (assuming the F- and AlF3/NaF products) or 14-15 and 26-28 kcal/mol, respectively (assuming the HF and AlF3OH-/NaFOH- products). nafoh 300-305 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 27455900-6 2016 Results from enzyme linked immunosorbent assays revealed that 1,8-cineole suppressed LPS-induced secretion of interleukin-6 and interleukin-8, and recovered nitric oxide to normal levels. Eucalyptol 62-73 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 27716424-7 2016 In BEAS-2B cells, both SE-A and SE-R inhibited the increase in production of the inflammatory cytokines IL-6 and IL-8. se-a 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 27125951-3 2016 Additional tracers such as 18F-sodium fluoride (18F-NaF) provide additional avenues for characterizing atherosclerosis development. 18f-sodium fluoride 27-46 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 27739445-6 2016 Using ex vivo human CRC explants, quininib significantly reduced the secretions of IL-6, IL-8, VEGF, ENA-78, GRO-alpha, TNF, IL-1beta and MCP-1 ex vivo (all values p < 0.01). quininib 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 27716424-7 2016 In BEAS-2B cells, both SE-A and SE-R inhibited the increase in production of the inflammatory cytokines IL-6 and IL-8. Serine 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 27705794-7 2016 Finally, gene expression and epistasis analysis indicated that CXCL8(IL-8) was a functional target of vitamin D3-mediated HSPC regulation. Cholecalciferol 102-112 C-X-C motif chemokine ligand 8 Homo sapiens 63-68 27705794-7 2016 Finally, gene expression and epistasis analysis indicated that CXCL8(IL-8) was a functional target of vitamin D3-mediated HSPC regulation. Cholecalciferol 102-112 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 27104742-11 2016 IL-6 and IL-8 release in unstimulated cultures was higher for CPT-isolated PBMCs compared to Ficoll- and SepMate-isolated PBMCs. sepmate 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 27867948-0 2016 Supra-therapeutic plasma concentrations of haloperidol induce moderate inhibition of lipopolysaccharide-induced interleukin-8 release in human monocytes. Haloperidol 43-54 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 27867948-4 2016 This study examined the effects of the mood-stabilizing drugs carbamazepine and valproic acid and of the antipsychotic drugs olanzapine, risperidone and haloperidol on the production of the pro-inflammatory chemokine interleukin-8 (IL-8), which is released from human monocytes when activated by Gram-negative lipopolysaccharide (LPS). Haloperidol 153-164 C-X-C motif chemokine ligand 8 Homo sapiens 217-230 27867948-4 2016 This study examined the effects of the mood-stabilizing drugs carbamazepine and valproic acid and of the antipsychotic drugs olanzapine, risperidone and haloperidol on the production of the pro-inflammatory chemokine interleukin-8 (IL-8), which is released from human monocytes when activated by Gram-negative lipopolysaccharide (LPS). Haloperidol 153-164 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 27867948-7 2016 RESULTS: At supra-therapeutic concentrations of 100 microM, haloperidol inhibited the LPS-induced release of IL-8 in peripheral human monocytes moderately, whereas olanzapine, risperidone, carbamazepine and valproic acid showed no such effect. Haloperidol 60-71 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 27455449-11 2016 Proteasome inhibitors, bortezomib and MG132, enhanced IL-8 production in both sides, apical and basolateral. Bortezomib 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 27455449-11 2016 Proteasome inhibitors, bortezomib and MG132, enhanced IL-8 production in both sides, apical and basolateral. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 27560195-7 2016 The polyphenol intervention significantly reduced the levels of VEGF, ROS, IL-8 and ICAM-1, with a more pronounced effect in TNF-alpha-activated endothelial cells. Polyphenols 4-14 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 27281236-6 2016 The results showed that OEA suppressed the expression of interleukin-6, interleukin-8, vascular adhesion molecule-1, and intercellular adhesion molecule-1 in a dose-dependent manner. N-oleoylethanolamine 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 72-85 27503790-6 2016 K1 inhibited both TNF- and phorbol 12-myristate 13-acetate (PMA)-induced NF-kappaB activation, as detected by transcription of synthetic (e.g. luciferase) and natural (e.g. CXCL8) genes controlled by NF-kappaB. Tetradecanoylphorbol Acetate 27-58 C-X-C motif chemokine ligand 8 Homo sapiens 173-178 27503790-6 2016 K1 inhibited both TNF- and phorbol 12-myristate 13-acetate (PMA)-induced NF-kappaB activation, as detected by transcription of synthetic (e.g. luciferase) and natural (e.g. CXCL8) genes controlled by NF-kappaB. Tetradecanoylphorbol Acetate 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 173-178 27423378-11 2016 Low IL-8 level (p=0.053) was marginally associated with platinum resistant disease. Platinum 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 27694173-6 2016 In summary, 18F-NaF PET/CT is a highly sensitive method, but 18F-fluorocholine PET/CT can detect early bone marrow metastases and provide greater specificity in the detection of bone metastases in patients with prostate cancer. Fluorine-18 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 27452280-0 2016 Human eosinophils are direct targets to nanoparticles: Zinc oxide nanoparticles (ZnO) delay apoptosis and increase the production of the pro-inflammatory cytokines IL-1beta and IL-8. Zinc Oxide 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 27599556-7 2016 Heparin also decreased the TNF-alpha-induced mRNA and protein expression levels of IL-6, IL-8, TNF-alpha and cyclin D1 in a dose-dependent manner. Heparin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 27473010-9 2016 CONCLUSION: MCZ may have preventive roles in the clinical management of IP in ELBWI by the suppression of IL-8 and HMGB-1. Miconazole 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 27427241-4 2016 Exposure to Cd(2+), Zn(2+) and As(3+) induced CXCL8 and IL-6 release at concentrations below 100muM, and Mn(2+) and Ni(2+) at concentrations above 200muM. Cadmium 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 46-51 27427241-4 2016 Exposure to Cd(2+), Zn(2+) and As(3+) induced CXCL8 and IL-6 release at concentrations below 100muM, and Mn(2+) and Ni(2+) at concentrations above 200muM. Zinc 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 46-51 27309886-0 2016 Effect of intravenous lidocaine combined with amitriptyline on pain intensity, clinical manifestations and the concentrations of IL-1, IL-6 and IL-8 in patients with fibromyalgia: A randomized double-blind study. Lidocaine 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 27206713-8 2016 RESULTS: Exposure of monocytes/macrophages to MSU crystals alone induced the moderate release of IL-8 but not of IL-1beta. Uric Acid 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 27427241-7 2016 The most potent metals, Cd(2+), Zn(2+) and As(3+) induced highest levels of oxidative activity, and ROS appeared to be central in their CXCL8 and IL-6 responses. Cadmium 24-26 C-X-C motif chemokine ligand 8 Homo sapiens 136-141 27427241-7 2016 The most potent metals, Cd(2+), Zn(2+) and As(3+) induced highest levels of oxidative activity, and ROS appeared to be central in their CXCL8 and IL-6 responses. Arsenic 43-45 C-X-C motif chemokine ligand 8 Homo sapiens 136-141 27427241-7 2016 The most potent metals, Cd(2+), Zn(2+) and As(3+) induced highest levels of oxidative activity, and ROS appeared to be central in their CXCL8 and IL-6 responses. ros 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 136-141 27427241-9 2016 However, the NF-kappaB pathway appeared predominately to be involved only in Zn(2+)- and As(3+)-induced CXCL8 and IL-6 responses. Zinc 77-79 C-X-C motif chemokine ligand 8 Homo sapiens 104-109 27452280-0 2016 Human eosinophils are direct targets to nanoparticles: Zinc oxide nanoparticles (ZnO) delay apoptosis and increase the production of the pro-inflammatory cytokines IL-1beta and IL-8. Zinc Oxide 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 27452280-7 2016 In addition, ZnO were found to increase the production of the proinflammatory IL-1beta and IL-8 cytokines. Zinc Oxide 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 27452280-8 2016 Using a pharmacological approach, we demonstrated that inhibition of caspase-1 reversed the ability of ZnO to induce IL-1beta and IL-8 production, whereas inhibition of caspase-4 only reversed that of IL-8. Zinc Oxide 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 27108256-8 2016 The independent sensing platform of Fe(2+), Fe(3+), and Cu(2+)could be established by using NaF as a complexing agent and by regulating the reaction time between NaF and metal ions. ammonium ferrous sulfate 36-42 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 27040396-8 2016 Interestingly, the latter response was driven by CXCL8 autocrine signaling because it was abolished by SB225002, an antagonist that prevents CXCL8 from binding to CXCR2. SB 225002 103-111 C-X-C motif chemokine ligand 8 Homo sapiens 49-54 27040396-8 2016 Interestingly, the latter response was driven by CXCL8 autocrine signaling because it was abolished by SB225002, an antagonist that prevents CXCL8 from binding to CXCR2. SB 225002 103-111 C-X-C motif chemokine ligand 8 Homo sapiens 141-146 27531902-9 2016 IL-8 released by cancer cells also activated pancreatic stellate cell (PSC) to increase GEM resistance. gemcitabine 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 27296843-3 2016 SMG was either incorporated within the alginate microbeads or used as a secondary coat on poly-l-lysine (PLL)-containing microcapsules, resulting in reduction of the inflammatory cytokines (IL-1beta, TNF, IL-6, IL-8, MIP-1alpha). N-SUCCINYL METHIONINE 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. beta-pinene 43-54 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. beta-pinene 43-54 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. sabinene 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. sabinene 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. gamma-terpinene 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. gamma-terpinene 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. geranylacetone 83-97 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. geranylacetone 83-97 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. pichtosin 103-120 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 27586050-4 2016 In addition, treatment of neutrophils with beta-pinene, sabinene, gamma-terpinene, geranylacetone, and isobornyl acetate desensitized the cells to N-formyl-Met-Leu-Phe (fMLF)- and interleukin-8 (IL-8)-induced [Ca(2+)]i flux and inhibited fMLF-induced chemotaxis. pichtosin 103-120 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 27586050-7 2016 In contrast, myristicin inhibited neutrophil [Ca(2+)]i flux stimulated by fMLF and IL-8 and inhibited capsaicin-induced Ca(2+) influx in TRPV1-transfected HEK293 cells. myristicin 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 27108256-8 2016 The independent sensing platform of Fe(2+), Fe(3+), and Cu(2+)could be established by using NaF as a complexing agent and by regulating the reaction time between NaF and metal ions. ammonium ferrous sulfate 36-42 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 27108256-8 2016 The independent sensing platform of Fe(2+), Fe(3+), and Cu(2+)could be established by using NaF as a complexing agent and by regulating the reaction time between NaF and metal ions. ferric sulfate 44-50 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 27108256-8 2016 The independent sensing platform of Fe(2+), Fe(3+), and Cu(2+)could be established by using NaF as a complexing agent and by regulating the reaction time between NaF and metal ions. ferric sulfate 44-50 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 27108256-8 2016 The independent sensing platform of Fe(2+), Fe(3+), and Cu(2+)could be established by using NaF as a complexing agent and by regulating the reaction time between NaF and metal ions. cupric ion 56-62 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 27108256-8 2016 The independent sensing platform of Fe(2+), Fe(3+), and Cu(2+)could be established by using NaF as a complexing agent and by regulating the reaction time between NaF and metal ions. cupric ion 56-62 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 27108256-8 2016 The independent sensing platform of Fe(2+), Fe(3+), and Cu(2+)could be established by using NaF as a complexing agent and by regulating the reaction time between NaF and metal ions. Metals 170-175 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 27108256-8 2016 The independent sensing platform of Fe(2+), Fe(3+), and Cu(2+)could be established by using NaF as a complexing agent and by regulating the reaction time between NaF and metal ions. Metals 170-175 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 27397760-8 2016 In conclusion, ceftaroline is able to counteract the effects of CSE on the innate immunity and pro-inflammatory responses modulating TLR2, LPS binding, NFkB activation and activity, HBD2 and IL-8 expression in bronchial epithelial cells. T 91825 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 27604412-6 2016 The ensuing Ca(2+) entry then activates NFAT/calcineurin signaling to induce transcriptional production of the proinflammatory cytokines IL-6 and IL-8. nfat 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 27515449-2 2016 Previous studies have demonstrated that both TLR2 agonists Pam3CSK4 and PGN stimulated IL-8 release in human mast cells. pgn 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 28028949-10 2016 CONCLUSIONS: In COP patients, response to clarithromycin treatment was associated with decreases in serum concentrations of IL-6, IL-8 and TGF-beta, and of rations, and of the BAL-f concentration of IL-6. Clarithromycin 42-56 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 27397760-6 2016 Ceftaroline counteracted the CSE effect on TLR2 expression, on LPS binding, on IL-8 mRNA, HBD2 and NFkB in 16HBE. T 91825 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 27490211-12 2016 Tideglusib reported a significant dose-dependent increase in pro-apoptotic proteins (PARP, Caspase-9, Caspase-7, Caspase-3) and tumor-related genes (FasL, TNF-alpha, Cox-2, IL-8, Caspase-3). tideglusib 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 27260851-7 2016 Besides, DHEA inhibited the anchorage-independent growth on agar and decreased the size of spheroids, and also reduced the secretion of IL-1alpha, IL-6, IL-8, and TNF-alpha in all cell lines. Dehydroepiandrosterone 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 26641773-4 2016 In this study, we demonstrate that treatment of HL-60 cells with allopurinol significantly increased the mRNA expression levels of interleukin-8, monocyte chemotactic protein-1 and tumor necrosis factor alpha in a time- and concentration-dependent manner. Allopurinol 65-76 C-X-C motif chemokine ligand 8 Homo sapiens 131-144 27759405-3 2016 24 patients of the test group (TG) rinsed after tooth brushing with a fluoride mouth rinse (100 ppm AmF/150 ppm NaF) while 21 patients of the control group (CG) did not. fluoride mouth rinse 70-90 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 27593287-8 2016 Cr was positively correlated with both IL-6 and IL-8 release, while Si was only associated with the increase of IL-6. Chromium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 27904616-7 2016 After folic acid and metformin administration, mean of Hcy, HOMA-IR, TNF-alpha, and IL-8 decreased significantly (P < 0.05). Folic Acid 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 27904616-7 2016 After folic acid and metformin administration, mean of Hcy, HOMA-IR, TNF-alpha, and IL-8 decreased significantly (P < 0.05). Metformin 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 27515207-7 2016 Thus, gelsolin inhibits the release of IL-8 from human neutrophils subjected to lipoteichoic acid, lipopolysaccharide and heat-inactivated bacteria treatment. lipoteichoic acid 80-97 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 27588140-6 2016 Furthermore, IL-8 could induce AKT phosphorylation, and the phosphatidylinositol-4,5-bisphosphate 3-kinase inhibitor LY294002 could inhibit the EMT of RCC cells that was induced by IL-8. phosphatidylinositol-4, 60-83 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 27484716-7 2016 The results demonstrated that celastrol significantly attenuated the expression of IL-6, IL-8, cyclooxygenase (COX)-2 and intercellular adhesion molecule-1 (ICAM-1), and inhibited IL-1beta-induced increases in the expression of IL-6, IL-8, ICAM-1 and COX-2. celastrol 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 27484716-7 2016 The results demonstrated that celastrol significantly attenuated the expression of IL-6, IL-8, cyclooxygenase (COX)-2 and intercellular adhesion molecule-1 (ICAM-1), and inhibited IL-1beta-induced increases in the expression of IL-6, IL-8, ICAM-1 and COX-2. celastrol 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 27171647-0 2016 High glucose-induced oxidative stress increases IL-8 production in human gingival epithelial cells. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 27171647-7 2016 Increased IL-8 secretion in HG was inhibited by pretreatment with an antioxidant, N-acetylcysteine, or a protein kinase C inhibitor, Ro31-8220. Acetylcysteine 82-98 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 27171647-7 2016 Increased IL-8 secretion in HG was inhibited by pretreatment with an antioxidant, N-acetylcysteine, or a protein kinase C inhibitor, Ro31-8220. Ro 31-8220 133-142 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 28390203-10 2016 The addition of stannous fluoride suppressed production of TNF-a, IFN-g, IL12p70, IL10, IL-1b, IL2, and IL-6, and also increased secretion of Il-8 in dose response fashion. Tin Fluorides 16-33 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 27540423-8 2016 The applications of F-18 fluorodeoxyglucose (FDG) and F-18 sodium fluoride (NaF) to cardiovascular diseases have revealed details on the basic pathophysiology of ischemic heart diseases. f-18 sodium fluoride 54-74 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 27588140-6 2016 Furthermore, IL-8 could induce AKT phosphorylation, and the phosphatidylinositol-4,5-bisphosphate 3-kinase inhibitor LY294002 could inhibit the EMT of RCC cells that was induced by IL-8. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 117-125 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 27468646-4 2016 CAM treatment led to a significant reduction in poly I:C- and RSV-mediated IL-8, CCL5, IFN-beta and -lambda production. Clarithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 27468646-4 2016 CAM treatment led to a significant reduction in poly I:C- and RSV-mediated IL-8, CCL5, IFN-beta and -lambda production. Poly I 48-54 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 27473819-6 2016 By using pure compounds, we found that casuarictin may act as a pure NF-kappaB inhibitor while agrimoniin inhibits IL-8 secretion also acting on other biological targets; in our system procyanidin B1 prevents the TNFalpha-induced effects without interfering with the NF-kappaB pathway. agrimoniin 95-105 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 27468646-4 2016 CAM treatment led to a significant reduction in poly I:C- and RSV-mediated IL-8, CCL5, IFN-beta and -lambda production. Carbon 0-1 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 27216470-6 2016 Tannic acid-modified but not unmodified AgNPs down-regulated TNF-alpha and LPS-triggered production of IL-8 in VK2-E6/E7 but not in HaCaT cells. Tannins 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 29620823-12 2016 Duraphat (5%NaF) and Clinprotm(5%NaF+TCP) had the highestrelease of fluoride at 3-month evaluation. sodium fluoride topical preparation 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 29620823-12 2016 Duraphat (5%NaF) and Clinprotm(5%NaF+TCP) had the highestrelease of fluoride at 3-month evaluation. clinprotm 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 27311854-5 2016 Although gemcitabine also enhanced CXCL8 expression, anti-CXCL8 antibody failed to reduce gemcitabine-induced increases in SA beta-Gal-positive cell numbers. gemcitabine 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 29620823-12 2016 Duraphat (5%NaF) and Clinprotm(5%NaF+TCP) had the highestrelease of fluoride at 3-month evaluation. Fluorides 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 27557865-3 2016 This study aimed to compare dental stain control of twice-daily brushing with a sodium fluoride (NaF) dentifrice containing 67 % sodium bicarbonate (NaHCO3) or a commercially available NaF silica dentifrice without NaHCO3, while using a mouthwash containing 0.2 % CHX. Sodium Fluoride 80-95 C-X-C motif chemokine ligand 8 Homo sapiens 97-100 27557865-3 2016 This study aimed to compare dental stain control of twice-daily brushing with a sodium fluoride (NaF) dentifrice containing 67 % sodium bicarbonate (NaHCO3) or a commercially available NaF silica dentifrice without NaHCO3, while using a mouthwash containing 0.2 % CHX. Silicon Dioxide 189-195 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 27405388-4 2016 In this work, a high-throughput microfluidic platform was developed for the optimization of chromatographic conditions regarding the capture of an anti-interleukin 8 mAb, using a multimodal ligand (2-benzamido-4-mercaptobutanoic acid), under a wide range of buffer pH and conductivities. SCHEMBL2330376 198-233 C-X-C motif chemokine ligand 8 Homo sapiens 152-165 27571064-12 2016 p38 MAPK inhibitor SB239063 significantly attenuated IL-6 and IL-8 release the most (p <= 0.05). SB 239063 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 27301357-7 2016 In fact, the effect of bortezomib on IL-8 production was higher than that exerted by stromal-MM cell interactions. Bortezomib 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 27529418-7 2016 Additionally, miR-200c delivered using polyethylenimine (PEI) nanoparticles effectively inhibits IL-6, IL-8 and CCL-5 in primary human periodontal ligament fibroblasts and increases the biomarkers of osteogenic differentiation in human bone marrow mesenchymal stem cells (MSCs), including calcium content, ALP, and Runx2. Polyethyleneimine 39-55 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 27529418-7 2016 Additionally, miR-200c delivered using polyethylenimine (PEI) nanoparticles effectively inhibits IL-6, IL-8 and CCL-5 in primary human periodontal ligament fibroblasts and increases the biomarkers of osteogenic differentiation in human bone marrow mesenchymal stem cells (MSCs), including calcium content, ALP, and Runx2. Polyethyleneimine 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 27269729-4 2016 In this study, PF6 was shown to form unimodal nanocomplexes with miR-146a mimic that entered into human primary keratinocytes, where miR-146a inhibited the expression of its direct targets from the NF-kappaB pathway and the genes known to be activated by NF-kappaB, C-C motif ligand (CCL)5 and interleukin (IL)-8. pf6 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 294-312 27240956-4 2016 Under basal conditions CF cells had increased bromodomain (Brd)3 and Brd4 recruitment and enhanced NF-kappaB and C/EBPbeta binding to the CXCL8 promoter compared to non-CF cells due to trimethylation of histone H3 at lysine 4 (H3K4me3) and DNA hypomethylation at CpG6. Lysine 217-223 C-X-C motif chemokine ligand 8 Homo sapiens 138-143 27301357-6 2016 Interestingly, IL8 expression also increased in HMCLs, stromal cells, and osteoclasts after treatment with the antimyeloma drugs melphalan and bortezomib. Bortezomib 143-153 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 27216995-7 2016 Efavirenz induced a marked concentration-dependent increase in interleukin-8 expression and release whereas elvitregravir had little effect. efavirenz 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 27340129-0 2016 Ursodeoxycholic acid inhibits TNFalpha-induced IL-8 release from monocytes. Ursodeoxycholic Acid 0-20 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 27301549-1 2016 (18)F-sodium fluoride (NaF) as an imaging tracer portrays calcium metabolic activity either in the osseous structures or in soft tissue. Sodium Fluoride 6-21 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 27301549-6 2016 Several studies have evaluated the efficacy of bisphosphonates and their lasting effects as treatment for osteoporosis using bone turnover measured by NaF-PET. Diphosphonates 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 27301549-1 2016 (18)F-sodium fluoride (NaF) as an imaging tracer portrays calcium metabolic activity either in the osseous structures or in soft tissue. Calcium 58-65 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 27159450-4 2016 We developed a biocompatible, cationic polylactide (CPLA) nanocarrier to complex with and efficiently deliver IL-8 small interfering RNA (siRNA) to CaP cells in vitro and in vivo. poly(lactide) 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 27177354-15 2016 The induction of IL-8 in Beas-2B cells was significantly associated with Cu, Ni and Zn and endotoxin. Copper 73-75 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 27177354-15 2016 The induction of IL-8 in Beas-2B cells was significantly associated with Cu, Ni and Zn and endotoxin. Zinc 84-86 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 27159450-4 2016 We developed a biocompatible, cationic polylactide (CPLA) nanocarrier to complex with and efficiently deliver IL-8 small interfering RNA (siRNA) to CaP cells in vitro and in vivo. cpla 52-56 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 27312705-5 2016 First, NS-398, instead of reducing inflammation, appeared to further enhance IL-1beta-mediated COX-2 and IL-8 production. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 7-13 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 27312705-0 2016 Novel effects of the cyclooxygenase-2-selective inhibitor NS-398 on IL-1beta-induced cyclooxygenase-2 and IL-8 expression in human ovarian granulosa cells. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 58-64 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 27043920-12 2016 In addition, baicalin also inhibited the productions of inflammatory cytokines such as IL-1beta, IL-6, IL-8 and TNF-alpha and suppressed the phosphorylation of JAK2, STAT5, IKKbeta, IkappaBalpha and the nuclear translocation of NF-kappaB (p65) subunit in LPS-stimulated human mast cells. baicalin 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 27556215-7 2016 Further studies demonstrated that curcumin treatment (20 muM) significantly inhibited proinflammatory factors, including IL-6, ELAM-1, IL-1alpha, and IL-8, whereas it decreased activities of senescence marker SA-beta-gal, and lowered levels of carbonylated proteins and apoptotic cell numbers. Curcumin 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 27086089-11 2016 Plasma concentrations of IL-6, IL-8, and TNFalpha, and peritoneal concentrations of IL-6 and IL-8, were significantly lower in the simvastatin group postoperatively. Simvastatin 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 27086089-11 2016 Plasma concentrations of IL-6, IL-8, and TNFalpha, and peritoneal concentrations of IL-6 and IL-8, were significantly lower in the simvastatin group postoperatively. Simvastatin 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 27312705-8 2016 Flow cytometry analysis demonstrated that NS-398, in combination with IL-1beta, significantly enhanced cell cycle progression involving IL-8. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 26403145-2 2016 We emphasize the role of [18F]-sodium fluoride (NaF) PET/CT as a potential noninvasive tool to identify and differentiate the transthyretin-related cardiac amyloidosis from the light-chain cardiac amyloidosis. [18f]-sodium fluoride 25-46 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 27234962-7 2016 Furthermore, treatment with 24,25-[OH]2D3 increased IL-1beta, IL-6, and IL-8 expression by HepG2 cells. 24,25-Dihydroxyvitamin D 3 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 27278862-0 2016 MAPK pathways are involved in the inhibitory effect of berberine hydrochloride on gastric cancer MGC 803 cell proliferation and IL-8 secretion in vitro and in vivo. berberine chloride 55-78 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 26446985-7 2016 The gingival crevicular fluid IL-8 levels were significantly higher in the S-GAgP group compared with the N-GAgP group and in the S-CP group compared with the N-CP group (p < 0.05); differences between the SG and NG and the SH and NH groups were not statistically significant (p > 0.05). gagp 77-81 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 26446985-7 2016 The gingival crevicular fluid IL-8 levels were significantly higher in the S-GAgP group compared with the N-GAgP group and in the S-CP group compared with the N-CP group (p < 0.05); differences between the SG and NG and the SH and NH groups were not statistically significant (p > 0.05). n-gagp 106-112 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 27300134-10 2016 Moreover, palmitic acid stimulated caspase-3 activation and inflammatory cytokine secretion (e.g., IL-6 and IL-8). Palmitic Acid 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 27300134-12 2016 In addition, palmitic acid-induced IL-1beta, IL-6, and IL-8 secretion was depended on reactive oxygen species (ROS) generation. Palmitic Acid 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 27300134-12 2016 In addition, palmitic acid-induced IL-1beta, IL-6, and IL-8 secretion was depended on reactive oxygen species (ROS) generation. Reactive Oxygen Species 86-109 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 27300134-12 2016 In addition, palmitic acid-induced IL-1beta, IL-6, and IL-8 secretion was depended on reactive oxygen species (ROS) generation. Reactive Oxygen Species 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 27300134-13 2016 In conclusion, palmitic acid caused activation of NLRP3 inflammasomes and inflammatory responses, inducing IL-1beta, IL-6, and IL-8 secretion, which is associated with ROS generation, in human Sw.71 placental cells. Palmitic Acid 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 27278862-7 2016 However, there was no significant synergistic inhibitory effect of combined BER and evodiamine (EVO) treatment on tumorigenesis, and BER reduced the upregulation of IL-8 induced by EVO in vivo. evodiamine 181-184 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 27446449-3 2016 The data showed that atorvastatin decreased the visfatin-induced expression of interleukin (IL)-6 and IL-8 in HCAECs. Atorvastatin 21-33 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 27271044-5 2016 G1 inhibited the secretion of two proinflammatory cytokines, interleukin (IL)-6 and IL-8, in cells stimulated by adenosine 5"-(gamma-thio)triphosphate (ATPgammaS). adenosine 5'-O-(3-thiotriphosphate) 113-150 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 27271044-5 2016 G1 inhibited the secretion of two proinflammatory cytokines, interleukin (IL)-6 and IL-8, in cells stimulated by adenosine 5"-(gamma-thio)triphosphate (ATPgammaS). adenosine 5'-O-(3-thiotriphosphate) 152-161 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 27467268-8 2016 Live imaging demonstrated that in WM-15-treated neutrophils, where homotypic aggregation was evident, the number of cells entering IL-8 impregnated collagen I gels was significantly reduced. wm-15 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 27406216-9 2016 Significant differences in basal KC cytokine secretion (IL-1alpha, IL-18, and CXCL8) were only observed between KC-Prim and KC-HPV. kc-hpv 124-130 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 27335135-4 2016 TP/BF showed highest microTBS, while NaF polymers decreased microTBS. microtbs 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 27335135-7 2016 NaF addition enhanced acid resistance but decreased microTBS. microtbs 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 27455959-10 2016 In patients, prednisolone abolished symptoms, normalized C-reactive protein, and reduced melatonin, IL-6, IL-8, and TNF-alpha concentrations (2P < 0.05), while IL-10 increased between 10:00 and 14:00. Prednisolone 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 27453994-6 2016 Treatment with the inflammatory agents lipopolysaccharide (LPS) or palmitate augmented the secretion of many myokines including: GROa, IL6, IL8, IL15, and TNFa, but did not consistently alter the protein content and/or phosphorylation of IkBa, p44/42 MAPK, p38 MAPK, c-Jun N-terminal kinase (JNK) and NF-kB, nor lead to consistent changes in basal and insulin-stimulated glucose uptake or free fatty acid oxidation. Palmitates 67-76 C-X-C motif chemokine ligand 8 Homo sapiens 140-143 27430279-5 2016 Cholesterol and sphingomyelin-containing liposomes designed to sequester pneumolysin were highly effective at reducing CXCL8 levels from epithelial cells exposed to different clinical pneumococcal isolates. Cholesterol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 119-124 27389658-3 2016 Here, for the first time, we address the electrochemical actuation and the associated stress-charge coefficients of bulk nanoporous nickel (np-Ni) in both strongly (NaOH) and weakly (NaF) adsorbed electrolytes. Nickel 132-138 C-X-C motif chemokine ligand 8 Homo sapiens 183-186 27430279-5 2016 Cholesterol and sphingomyelin-containing liposomes designed to sequester pneumolysin were highly effective at reducing CXCL8 levels from epithelial cells exposed to different clinical pneumococcal isolates. Sphingomyelins 16-29 C-X-C motif chemokine ligand 8 Homo sapiens 119-124 27312995-8 2016 Acidic stimulation increased IL-8 production in LECs, whereas a selective transient receptor potential vanilloid subtype 1 (TRPV1) antagonist, 5"-iodoresiniferatoxin, decreased IL-8 production. iodoresiniferatoxin 143-165 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 27436995-5 2016 RESULTS: At the non-toxic dosages, chemical compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics dose-dependently increased IL-8 reporter gene expression. Nicotine 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 27436995-5 2016 RESULTS: At the non-toxic dosages, chemical compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics dose-dependently increased IL-8 reporter gene expression. aromatic amines 77-92 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 27436995-5 2016 RESULTS: At the non-toxic dosages, chemical compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics dose-dependently increased IL-8 reporter gene expression. Benzopyrenes 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 27436995-5 2016 RESULTS: At the non-toxic dosages, chemical compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics dose-dependently increased IL-8 reporter gene expression. Phenols 107-114 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 27436995-5 2016 RESULTS: At the non-toxic dosages, chemical compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics dose-dependently increased IL-8 reporter gene expression. Aldehydes 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Nicotine 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Nicotine 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 326-330 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. aromatic amines 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. aromatic amines 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 326-330 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Benzopyrenes 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Benzopyrenes 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 326-330 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Phenols 96-103 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Phenols 96-103 C-X-C motif chemokine ligand 8 Homo sapiens 326-330 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Aldehydes 105-114 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Aldehydes 105-114 C-X-C motif chemokine ligand 8 Homo sapiens 326-330 27436995-6 2016 Consistently, the representative compounds belonging to nicotine, aromatic amines, benzopyrene, phenols, aldehydes, and some other volatile organics significantly and dose-dependently increased IL-8 levels in the culture supernatants of 16HBE cells, among these compounds, benzopyrene is a most potent stimulator for inducing IL-8 production. Benzopyrenes 273-284 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 28955928-4 2016 Recent studies have demonstrated that cobalt ions from metal-on-metal joints also activate human TLR4, increasing cellular secretion of inflammatory chemokines including interleukin-8 (IL-8, CXCL8) and CCL2. Cobalt 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 170-183 28955928-4 2016 Recent studies have demonstrated that cobalt ions from metal-on-metal joints also activate human TLR4, increasing cellular secretion of inflammatory chemokines including interleukin-8 (IL-8, CXCL8) and CCL2. Cobalt 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 191-196 28955928-4 2016 Recent studies have demonstrated that cobalt ions from metal-on-metal joints also activate human TLR4, increasing cellular secretion of inflammatory chemokines including interleukin-8 (IL-8, CXCL8) and CCL2. Metals 55-60 C-X-C motif chemokine ligand 8 Homo sapiens 170-183 27415000-11 2016 Importantly, stimulated expression of IL-1beta and IL-8 in HaCaT-TNF-alpha were blocked by Quercetin, a flavanol shown to possess anti-TNF-alpha activities. Quercetin 91-100 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 27415000-11 2016 Importantly, stimulated expression of IL-1beta and IL-8 in HaCaT-TNF-alpha were blocked by Quercetin, a flavanol shown to possess anti-TNF-alpha activities. flavanol 104-112 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 28955928-4 2016 Recent studies have demonstrated that cobalt ions from metal-on-metal joints also activate human TLR4, increasing cellular secretion of inflammatory chemokines including interleukin-8 (IL-8, CXCL8) and CCL2. Metals 55-60 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 28955928-4 2016 Recent studies have demonstrated that cobalt ions from metal-on-metal joints also activate human TLR4, increasing cellular secretion of inflammatory chemokines including interleukin-8 (IL-8, CXCL8) and CCL2. Metals 55-60 C-X-C motif chemokine ligand 8 Homo sapiens 191-196 28955928-4 2016 Recent studies have demonstrated that cobalt ions from metal-on-metal joints also activate human TLR4, increasing cellular secretion of inflammatory chemokines including interleukin-8 (IL-8, CXCL8) and CCL2. Cobalt 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 26990648-0 2016 The differential effects of 1,25-dihydroxyvitamin D3 on Salmonella-induced interleukin-8 and human beta-defensin-2 in intestinal epithelial cells. Calcitriol 28-52 C-X-C motif chemokine ligand 8 Homo sapiens 75-88 28773666-7 2016 The biosensor based on TiO2/NAF/LAC presented the best electro-chemical properties with regard to sensitivity, stability and detection limit after a period of 22 days. titanium dioxide 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 28773666-7 2016 The biosensor based on TiO2/NAF/LAC presented the best electro-chemical properties with regard to sensitivity, stability and detection limit after a period of 22 days. lac 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 27248176-0 2016 IL-8 signaling is involved in resistance of lung carcinoma cells to erlotinib. Erlotinib Hydrochloride 68-77 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 27248176-4 2016 We report here that generation of erlotinib-resistant lung cancer cells in vitro resulted in a phenotypic alteration reminiscent of an epithelial-mesenchymal transition (EMT) concomitant with a robust upregulation of the IL-8/IL-8R axis. Erlotinib Hydrochloride 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 27248176-5 2016 Our results also demonstrate that upregulation of p38 MAPK signaling is responsible for the enhanced IL-8 secretion in the erlotinib-resistant tumor cells. Erlotinib Hydrochloride 123-132 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 27248176-6 2016 Blockade of IL-8 signaling effectively reduced mesenchymal features of the resistant cells and also markedly enhanced their susceptibility to erlotinib. Erlotinib Hydrochloride 142-151 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 25532488-6 2016 OTA-induced NO, TNF-alpha, IL-6, and IL-8 were significantly reduced in the quercetin pretreated samples indicating its anti-inflammatory role. Quercetin 76-85 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 26997430-5 2016 As a bone-specific tracer, there is accumulating evidence to support the use of sodium (18)F-fluoride ((18)F-NaF) PET-CT in the diagnosis of skeletal metastases in breast and prostate cancer, although relatively little data are available to support its use for assessment of treatment response. sodium (18)f-fluoride 80-101 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 27118044-7 2016 Although there is no evidence that AML pathophysiology is related to hypoxia, leukemic blasts still show several distinct biological features when exposed to reduced pO2: they down- or upregulate membrane receptors such as CXCR4 or FLT3, activate or inhibit intracellular signaling pathways such as PI3K, and specifically secrete cytokines (IL-8). PO-2 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 341-345 27347105-1 2016 The aim of the retrospective study was to analyze the effect of pioglitazone on the expression of tumor tissue inflammation factor interleukin (IL)-8, macrophage colony-stimulating factor (M-CSF) and vascular endothelial growth factor (VEGF) of type II diabetes in bladder cancer patients. Pioglitazone 64-76 C-X-C motif chemokine ligand 8 Homo sapiens 131-149 27120567-4 2016 The assay was compared to a bioassay in which tumor necrosis factor-alpha-induced interleukin-8 secretion from HT-29 cells was assessed after addition of IFX to ADA-containing sera or control sera. N-(2-acetamido)iminodiacetic acid 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 27308826-10 2016 Interestingly, there was a mean increase in all inflammatory cytokines (IL-1beta, IL-6, and IL-8) during the saline treatment from day 1 to week 3, whereas during the Tyloxapol treatment, all cytokines decreased. Sodium Chloride 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 27018308-4 2016 Furthermore, we found that TAM-derived CXCL8 mediated the loss of ERalpha and cancer invasion via HOXB13. tam 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 39-44 27106081-7 2016 The bromodomain inhibitors effectively decreased etoposide-induced release of IL-6 and IL-8. Etoposide 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 27210890-7 2016 KEY FINDINGS: RA significantly inhibited poly(I:C)-induced expression of inflammatory cytokines including IL-1beta, IL-6, IL-8, CCL20, and TNF-alpha, and downregulated NF-kappaB signaling pathway in human keratinocytes. rosmarinic acid 14-16 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 27210890-7 2016 KEY FINDINGS: RA significantly inhibited poly(I:C)-induced expression of inflammatory cytokines including IL-1beta, IL-6, IL-8, CCL20, and TNF-alpha, and downregulated NF-kappaB signaling pathway in human keratinocytes. Poly I-C 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 27076634-8 2016 Although dexamethasone treatment reduced RNA polymerase II occupancy of TNF targets such as IL8 and TNFAIP2, we were unable to correlate specific binding sequences for GR or occupancy patterns with repressive effects on transcription. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 27393034-0 2016 Carbon monoxide releasing molecule-2 ameliorates IL-1beta-induced IL-8 in human gastric cancer cells. Carbon Monoxide 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 27393034-8 2016 Pharmacological inhibition and mutagenesis studies indicated that NOX, ROS, Erk1/2, and p38 MAPK are involved in IL-1beta-induced IL-8 expression. Reactive Oxygen Species 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 27393034-11 2016 CORM-2 pretreatment significantly mitigated IL-1beta-induced activation of ROS/NF-kB and Erk1/2/AP-1 cascades, blocking IL-8 expression and thus significantly reducing endothelial cell proliferation in the tumor microenvironment. Reactive Oxygen Species 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 26347463-7 2016 CONCLUSION: Higher intakes of total cholesterol and saturated FA seem to correlate with increased serum IL8 levels, being a possible mechanism by which this pro-atherogenic intake pattern may increase the risk of age-related chronic diseases with important inflammatory contribution. Cholesterol 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 27622485-0 2016 Dendritic cells generated in the presence of vitamin D3 and stimulated with lipopolysaccharide secrete IL-8, IL-1beta, IL-10 and induce relatively low levels of CD4+CD25hiFoxp3+ T cells. Cholecalciferol 45-55 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 26574643-0 2016 Theophylline Represses IL-8 Secretion from Airway Smooth Muscle Cells Independently of Phosphodiesterase Inhibition. Theophylline 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 26574643-8 2016 However, theophylline (at 10 muM) was antiinflammatory and repressed secretion of the neutrophil chemoattractant cytokine IL-8, which is produced in response to TNF-alpha. Theophylline 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 26342602-13 2016 In HSC-2 cells, Glandosane significantly increased CXCL8 expression. Glandosane 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 52-57 27056727-9 2016 Hydrocortisone significantly attenuated IL-1beta-induced inflammatory responses in the immature human gut when administered at the time of the proinflammatory insult: IL-1beta-induced IL-8 and IL-6 secretion in the fetal ileum as well as H4 cells were significantly reduced. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 27056727-10 2016 Hydrocortisone also inhibited IL-8 secretion in response to TNF-alpha. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 26894321-7 2016 KEY RESULTS: Sulindac inhibited the transcriptional activity of NF-kappaB and decreased IL-8 transcription and secretion in TNF-alpha stimulated CF cells via a cyclooxygenase-independent mechanism. Sulindac 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 26993523-3 2016 A preconditioning of 18% CS also increased in a time-dependent fashion the release of soluble ICAM1 (sICAM1) and IL-8. Cesium 25-27 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 27473957-7 2016 Our results indicated that the isoquercitrin treatment of PMACI-stimulated KU812 cells significantly reduced the production of histamine and the pro-inflammatory cytokines, such as interleukin (IL)-6, IL-8, IL-1beta, and tumor necrosis factor (TNF)-alpha. isoquercitrin 31-44 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 27473957-7 2016 Our results indicated that the isoquercitrin treatment of PMACI-stimulated KU812 cells significantly reduced the production of histamine and the pro-inflammatory cytokines, such as interleukin (IL)-6, IL-8, IL-1beta, and tumor necrosis factor (TNF)-alpha. pmaci 58-63 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. n-octadecyl mercaptan 71-86 C-X-C motif chemokine ligand 8 Homo sapiens 41-46 26342602-16 2016 Epithelial cells have a differential response to artificial saliva with Glandosane changing CXCL8 expression. Glandosane 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. amino undecanethiol 121-140 C-X-C motif chemokine ligand 8 Homo sapiens 41-46 27072015-6 2016 Shikonin prevented IL-1beta- or tumor necrosis factor (TNF)-alpha-mediated IL-6, IL-8, and CCL20 production in HPDLC. shikonin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. amino undecanethiol 121-140 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. amino undecanethiol 121-140 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. Heparin 184-191 C-X-C motif chemokine ligand 8 Homo sapiens 41-46 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. Heparin 184-191 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. Heparin 184-191 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. Aminothiol 195-205 C-X-C motif chemokine ligand 8 Homo sapiens 41-46 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. Aminothiol 195-205 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 26970827-6 2016 We could show that more cells adhered to CXCL8 adsorbed to hydrophobic octadecanethiol than on CXCL8 covalently bound to amino undecanethiol or CXCL8 specifically bound to immobilized heparin on aminothiol. Aminothiol 195-205 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 27170049-10 2016 Orbital fibroblasts expressed HRH1 and loratadine and SC-514 both blocked histamine-induced IL-6, IL-8 and CCL2 production by orbital fibroblasts. SC 514 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 27170049-10 2016 Orbital fibroblasts expressed HRH1 and loratadine and SC-514 both blocked histamine-induced IL-6, IL-8 and CCL2 production by orbital fibroblasts. Histamine 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 27016717-0 2016 Oleic acid, hydroxytyrosol and n-3 fatty acids collectively modulate colitis through reduction of oxidative stress and IL-8 synthesis; in vitro and in vivo studies. Oleic Acid 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 27016717-0 2016 Oleic acid, hydroxytyrosol and n-3 fatty acids collectively modulate colitis through reduction of oxidative stress and IL-8 synthesis; in vitro and in vivo studies. 3,4-dihydroxyphenylethanol 12-26 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 27016717-0 2016 Oleic acid, hydroxytyrosol and n-3 fatty acids collectively modulate colitis through reduction of oxidative stress and IL-8 synthesis; in vitro and in vivo studies. Fatty Acids, Omega-3 31-46 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 27016717-3 2016 Caco-2 cells grown in medium chain fatty acids enriched medium has exaggerated t-butyl hydroperoxide induced cell damage, GSH depletion, and IL-1beta induced IL-8 synthesis, compared to the cells grown in oleic acid & hydroxytyrosol (OT) enriched medium. chain fatty acids 29-46 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 27016717-4 2016 Further, combined treatment of cells with eicosapentaenoic acid, docosahexaenoic acid, and OT has remarkably attenuated the cell damage, and IL-8 synthesis, compared to individual treatments. Eicosapentaenoic Acid 42-63 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 27016717-4 2016 Further, combined treatment of cells with eicosapentaenoic acid, docosahexaenoic acid, and OT has remarkably attenuated the cell damage, and IL-8 synthesis, compared to individual treatments. Docosahexaenoic Acids 65-85 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 27170049-9 2016 Histamine stimulated the production of IL-6, IL-8 and CCL2 by orbital fibroblasts, while it had no effect on the production of CCL5, CCL7, CXCL10, CXCL11 and hyaluronan. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 27170049-10 2016 Orbital fibroblasts expressed HRH1 and loratadine and SC-514 both blocked histamine-induced IL-6, IL-8 and CCL2 production by orbital fibroblasts. Loratadine 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 26644386-11 2016 The production of TNF-alpha, IL-1beta, and IL-8 by monocytes from PBC patients after stimulation with lipopolysaccharide and lipoteichoic acid was significantly increased when TIPE2 was knocked down. lipoteichoic acid 125-142 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 27035829-11 2016 RESULTS: In vitro studies showed that 1,25(OH)2D3 significantly reduced IL-1beta- or TNF-alpha-induced inflammatory responses, such as IL-8 expression and prostaglandin activity. Calcitriol 38-49 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 26641976-18 2016 No significant change was observed in the IL-8 profile in tryptophan-treated U251 cells except that L-kynurenine at 10 microg/mL produced significantly high level of an inflammatory cytokine IL-8. Kynurenine 100-112 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 27038552-7 2016 Antagomir-mediated inactivation of miR-424-5p prevented the IL-8-induced cell migration and invasion, indicating that miR-424-5p is required for IL-8-induced cellular invasiveness. -424-5p 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 26701134-9 2016 In vitro culture with supernatants from cortisol-treated peripheral blood monocyte-derived macrophages resulted in altered endometrial endothelial cell expression of the angiogenic genes, CXCL2, CXCL8, CTGF, and VEGFC These data highlight the importance of local cortisol in regulating paracrine actions of macrophages in the endometrium. Hydrocortisone 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 195-200 26944408-14 2016 Finally, aloin pretreatment also inhibited saliva-induced IL-8 production. alloin 9-14 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 26944408-15 2016 CONCLUSIONS: Results indicated that IL-1beta in saliva stimulates epithelial cells to produce IL-8 and that aloin effectively inhibits salivary IL-1beta-induced IL-8 production by mitigating the p38 and ERK pathway. alloin 108-113 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 27145239-10 2016 LCFA (oleic acid) up-regulated tumor necrosis fator-alpha, monocyte chemoattractant-1 and interleukin-1beta while down-regulated IL-6 and IL-8 secretion to a higher extent than MCFA in mRNA and protein levels. lcfa 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 27145239-10 2016 LCFA (oleic acid) up-regulated tumor necrosis fator-alpha, monocyte chemoattractant-1 and interleukin-1beta while down-regulated IL-6 and IL-8 secretion to a higher extent than MCFA in mRNA and protein levels. Oleic Acid 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 26823290-8 2016 After 24 h pre-treatment with 5 muM laquinimod, manHD monocytes released lower levels of IL-1beta, IL-5, IL-8, IL-10, IL-13 and TNFalpha in response to stimulation. 5 mum laquinimod 30-46 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 26944408-0 2016 Aloin Inhibits Interleukin (IL)-1beta-Stimulated IL-8 Production in KB Cells. alloin 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 26944408-2 2016 This study investigates stimulatory effects of salivary IL-1beta in IL-8 production and determines if aloin inhibits IL-1beta-stimulated IL-8 production in epithelial cells. alloin 102-107 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 26944408-8 2016 KB cells were pretreated with aloin, and its effect on IL-1beta-induced IL-8 production was examined by ELISA and Western blot analysis. alloin 30-35 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 26944408-13 2016 Aloin pretreatment inhibited IL-1beta-induced IL-8 production in a dose-dependent manner and inhibited activation of the p38 and ERK signaling pathway. alloin 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 27038552-7 2016 Antagomir-mediated inactivation of miR-424-5p prevented the IL-8-induced cell migration and invasion, indicating that miR-424-5p is required for IL-8-induced cellular invasiveness. -424-5p 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 27188901-10 2016 In addition, HMB supplementation was likely (78%-87% likelihood) to reduce interferon-gamma, interleukin 8, CX3CL1, and increase muscle volume for the adductor magnus (77% likelihood) compared to PL. beta-hydroxyisovaleric acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 93-106 27131284-9 2016 However, dabigatran at low concentrations (3-300nM) increased significantly the expression levels of CXCL1, CXCL2, IL-8, ELAM-1, MCP-1, and tissue factor. Dabigatran 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 27262815-7 2016 Moreover, PFKFB3 modulated toll like receptor 4 (TLR4) and MyD88 expression as well as interleukin (IL)-6 and IL-8 release from breast cancer cells in response to paclitaxel exposure. Paclitaxel 163-173 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 27262815-9 2016 The enhanced lactate contributed to TLR4 signaling activation, IL-6 and IL-8 generation, and cell viability promotion in MCF-7 cells. Lactic Acid 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 27229886-7 2016 In immortalized human airway smooth muscle (ASM) cells, Sul-121 dose-dependently prevented cigarette smoke extract-induced IL-8 release parallel with inhibition of nuclear translocation of the NF-kappaB subunit, p65 (each ~90%). Sulfisoxazole 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 27223137-3 2016 The amount of F and TMP released were directly related to NaF and TMP concentrations in the varnishes. trimetaphosphoric acid 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 27162363-4 2016 Using an in vitro model of colonic epithelial cells challenged with Escherichia coli K12, we showed that inhibition of histone deacetylases (HDAC) by trichostatin A dramatically enhanced induction of HBD2 expression, without affecting expression of IL-8. trichostatin A 150-164 C-X-C motif chemokine ligand 8 Homo sapiens 249-253 27223137-5 2016 However, the simultaneous addition of NaF and TMP to varnishes significantly reduced the amount of F and TMP released from the products. trimetaphosphoric acid 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 27274225-2 2016 In primary bronchial epithelial cells, exposure of toll-like receptor (TLR) ligands or tumor necrosis factor-alpha (TNF-alpha) increased TLR2 mRNA expression and reduced interleukin-8 (IL-8) release when coincubated with glucocorticosteroids. glucocorticosteroids 221-241 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 26926379-2 2016 Study shows that NaF:Mg,Cu,P phosphor possess good OSL properties having sensitivity comparable to that of commercially available Al2O3:C (Landauer Inc.). Magnesium 21-23 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 27146088-4 2016 Flagellin-induced interaction between the COOH region of Nox4 and the TIR domain of TLR5 led to H2O2 generation, which in turn promoted the secretion of pro-inflammatory cytokines including IL-8, as well as the expression of ICAM-1 in human aortic endothelial cells (HAECs). Hydrogen Peroxide 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 27140710-6 2016 Tumor necrosis factor alpha, IL-6 and IL-8 levels on the fourth day after treatment showed significant decrease in the somatostatin + ulinastatin, the somatostatin + gabexate and the somatostatin + ulinastatin + gabexate subgroups compared with the somatostatin subgroup. Gabexate 166-174 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 26926379-1 2016 OSL in doped NaF is studied. osl 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 26926379-2 2016 Study shows that NaF:Mg,Cu,P phosphor possess good OSL properties having sensitivity comparable to that of commercially available Al2O3:C (Landauer Inc.). p phosphor 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 26926379-2 2016 Study shows that NaF:Mg,Cu,P phosphor possess good OSL properties having sensitivity comparable to that of commercially available Al2O3:C (Landauer Inc.). osl 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 27383709-5 2016 RESULTS: Budlein A inhibited MPO activity, IL-6, CXCL8, IL-10, and IL-12 production and induces neutrophil apoptosis. budlein A 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 49-54 26960744-7 2016 Along with the lower levels of inflammatory cytokine gene expressions in the extract, treatment of the 2D IHOKs with Zn(2+) alone and treatment of the 3D IHOKs with Zn(2+) plus eugenol resulted in significantly lower expression levels of IL-1beta, IL-6, and IL-8 (P<0.05). Zinc 117-119 C-X-C motif chemokine ligand 8 Homo sapiens 258-262 26960744-7 2016 Along with the lower levels of inflammatory cytokine gene expressions in the extract, treatment of the 2D IHOKs with Zn(2+) alone and treatment of the 3D IHOKs with Zn(2+) plus eugenol resulted in significantly lower expression levels of IL-1beta, IL-6, and IL-8 (P<0.05). Zinc 165-167 C-X-C motif chemokine ligand 8 Homo sapiens 258-262 26960744-7 2016 Along with the lower levels of inflammatory cytokine gene expressions in the extract, treatment of the 2D IHOKs with Zn(2+) alone and treatment of the 3D IHOKs with Zn(2+) plus eugenol resulted in significantly lower expression levels of IL-1beta, IL-6, and IL-8 (P<0.05). Eugenol 177-184 C-X-C motif chemokine ligand 8 Homo sapiens 258-262 27269887-12 2016 Corticosteroids such as fluticasone propionate and dexamethasone, but not salmeterol, partially suppressed the IL-17A and TNF-alpha-induced IL-8 production. Fluticasone 24-46 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 27269887-12 2016 Corticosteroids such as fluticasone propionate and dexamethasone, but not salmeterol, partially suppressed the IL-17A and TNF-alpha-induced IL-8 production. Dexamethasone 51-64 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 26400651-6 2016 Chelation of Zn(2+) by the membrane permeable chelator N,N,N",N"-tetrakis-(2-pyridylmethyl)-ethylenediamine (TPEN) reduced granulocyte migration toward N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLF) and IL-8, indicating a role of free intracellular Zn(2+) in chemotaxis. Zinc 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 26400651-6 2016 Chelation of Zn(2+) by the membrane permeable chelator N,N,N",N"-tetrakis-(2-pyridylmethyl)-ethylenediamine (TPEN) reduced granulocyte migration toward N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLF) and IL-8, indicating a role of free intracellular Zn(2+) in chemotaxis. N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine 55-107 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 26400651-6 2016 Chelation of Zn(2+) by the membrane permeable chelator N,N,N",N"-tetrakis-(2-pyridylmethyl)-ethylenediamine (TPEN) reduced granulocyte migration toward N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLF) and IL-8, indicating a role of free intracellular Zn(2+) in chemotaxis. N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine 109-113 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 26400651-10 2016 TPEN inhibited the lipopolysaccharide-induced secretion of chemotactic IL-8 and also anti-inflammatory IL-1ra. N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 26647918-7 2016 In sharp contrast, dexamethasone left the local release of acute-phase mediators in the lungs virtually unchanged: bronchoalveolar lavage levels of IL-6 were only 18% lower and levels of IL-8 were even higher with dexamethasone compared with placebo, although the differences between treatments were not statistically significant (P = 0.07 and P = 0.08, respectively). Dexamethasone 214-227 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 27195204-2 2016 The present study aims to evaluate the in vivo effect of subgingivally delivered SMV gel (1.2 mg) as a local drug-delivery agent on clinical parameters and on interleukin-6 (IL-6), interleukin-8 (IL-8) and interleukin-10 (IL-10) levels in gingival crevicular fluid (GCF) of chronic periodontitis patients. Simvastatin 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 27195204-7 2016 RESULTS: SMV has an inhibitory effect on pro-inflammatory cytokines (IL-6, IL-8) and stimulatory effect on anti-inflammatory cytokines (IL-10) in GCF of periodontitis patients and has significantly positive effect on all clinical parameters except relative attachment level (RAL). Simvastatin 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 27038884-8 2016 KEY FINDINGS: IL-8 and IL-17A levels were higher in ISS from COPD patients and HSs than from HCs. ISS 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 26952447-4 2016 When the phosphoric acid solution contains NaF, fluorine is also incorporated into the oxide layer. phosphoric acid 9-24 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 27038884-8 2016 KEY FINDINGS: IL-8 and IL-17A levels were higher in ISS from COPD patients and HSs than from HCs. hepatic stimulator substance 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 27084536-0 2016 Thymoquinone inhibits growth of human medulloblastoma cells by inducing oxidative stress and caspase-dependent apoptosis while suppressing NF-kappaB signaling and IL-8 expression. thymoquinone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 26945908-0 2016 Suppression of IL-8-Src signalling axis by 17beta-estradiol inhibits human mesenchymal stem cells-mediated gastric cancer invasion. Estradiol 43-59 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 26945908-11 2016 We further observed that 17beta -estradiol inhibit HBMMSCS-induced cell motility via suppressing activation of IL8-Src signalling in human gastric cancer cells. Estradiol 25-42 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 26945908-12 2016 17beta-estradiol inhibits IL8-up-regulated Src downstream target proteins including p-Cas, p-paxillin, p-ERK1/2, p-JNK1/2, MMP9, tPA and uPA. Estradiol 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 26945908-12 2016 17beta-estradiol inhibits IL8-up-regulated Src downstream target proteins including p-Cas, p-paxillin, p-ERK1/2, p-JNK1/2, MMP9, tPA and uPA. p-paxillin 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 26945908-12 2016 17beta-estradiol inhibits IL8-up-regulated Src downstream target proteins including p-Cas, p-paxillin, p-ERK1/2, p-JNK1/2, MMP9, tPA and uPA. Tetradecanoylphorbol Acetate 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 26945908-13 2016 These results suggest that 17beta-estradiol significantly inhibits HBMMSCS-induced invasive motility through suppressing IL8-Src signalling axis in human gastric cancer cells. Estradiol 27-43 C-X-C motif chemokine ligand 8 Homo sapiens 121-124 26495785-8 2016 Controlling other independent factors, the relative hazard ratio for PDAC with higher IL-8-positive TIIC levels compared with those with lower TIIC levels was 1.588 (95% confidence interval, 1.04-2.42). pdac 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 27141896-7 2016 For an IQR increase in PM2.5, black carbon and PNC100-200, respective increases of 0.17 ng/ml (95% CI: 0.02-0.33), 0.12 ng/ml (95% CI: 0.01-0.24) and 0.13 ng/ml (95% CI:0.02-0.24) in interleukin-8 in EBC reflecting airway inflammation were also observed. Carbon 36-42 C-X-C motif chemokine ligand 8 Homo sapiens 183-196 27134560-1 2016 Understanding the range and variability of normal, benign degenerative, and malignant (18)F sodium fluoride ((18)F NaF) positron emission tomography/computed tomography (PET/CT) uptake is important in influencing clinical interpretation. Sodium Fluoride 92-107 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 27126933-7 2016 Effect of IL-8 overexpression on proliferation, cell cycle and migration in BT549 cells was respectively investigated by MTT assay, flow cytometry and wound-healing test. monooxyethylene trimethylolpropane tristearate 121-124 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 27128976-4 2016 18% CS increased surface expression of endothelial adhesion molecule ICAM1 and release of its soluble form (sICAM1) and inflammatory cytokine IL-8 by CS-stimulated pulmonary endothelial cells (EC). Cesium 4-6 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 27128976-4 2016 18% CS increased surface expression of endothelial adhesion molecule ICAM1 and release of its soluble form (sICAM1) and inflammatory cytokine IL-8 by CS-stimulated pulmonary endothelial cells (EC). Cesium 150-152 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 27128976-6 2016 Chronic exposure to 18% CS, but not to 5% CS, augmented ICAM1 and IL-8 production and EC monolayer barrier disruption induced by LPS. Cesium 24-26 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 27173229-7 2016 In a high-glucose environment, TLR-2/4 expression was significantly upregulated in RGCs (while their viability decreased); additionally, NF-kappaB expression and secretion of TNF-alpha and IL-8 were significantly increased. Glucose 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 27005483-7 2016 It is believed that the in situ formation of the active species of NaMgF3, NaF and Fe during the heating process could enhance the hydrogen storage properties of MgH2, due to the catalytic effects of these new species. Hydrogen 131-139 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 27005483-7 2016 It is believed that the in situ formation of the active species of NaMgF3, NaF and Fe during the heating process could enhance the hydrogen storage properties of MgH2, due to the catalytic effects of these new species. magnesium;hydride 162-166 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 27001463-5 2016 After treatment with nicotine (0.1-10 muM for 24 h), the HUVECs released chemotactic factors (IL-8) to attract monocytes into the tunica intima of the artery, and the monocytes then transformed into foam cells. Nicotine 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 27175089-7 2016 However, subjects with deficient levels of vitamin D and high CRP produced significantly higher levels of the proinflammatory cytokines (TNF-alpha and IL-8) as compared to subjects with low CRP levels with nondeficient and deficient levels of vitamin D. Vitamin D 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 26918409-1 2016 A carbonylative esterification reaction between aryl bromides and alcohols, promoted by Pd/C and NaF in the presence of oxiranes, has been developed. aryl bromides 48-61 C-X-C motif chemokine ligand 8 Homo sapiens 91-100 26918409-1 2016 A carbonylative esterification reaction between aryl bromides and alcohols, promoted by Pd/C and NaF in the presence of oxiranes, has been developed. Alcohols 66-74 C-X-C motif chemokine ligand 8 Homo sapiens 91-100 26918409-1 2016 A carbonylative esterification reaction between aryl bromides and alcohols, promoted by Pd/C and NaF in the presence of oxiranes, has been developed. Palladium 88-90 C-X-C motif chemokine ligand 8 Homo sapiens 91-100 26918409-1 2016 A carbonylative esterification reaction between aryl bromides and alcohols, promoted by Pd/C and NaF in the presence of oxiranes, has been developed. Epoxy Compounds 120-128 C-X-C motif chemokine ligand 8 Homo sapiens 91-100 27091625-5 2016 Transcriptomic profiling revealed the up-regulation of three NF-kappaB-regulated CXC-chemokines, CXCL8, CXCL1 and CXCL2, in the resistant cells that were more efficiently down-regulated after OXA + Curcumin treatment as compared to the sensitive cells. Curcumin 198-206 C-X-C motif chemokine ligand 8 Homo sapiens 97-102 27002382-6 2016 TE and betulin treatment led to increased mRNA levels of chemokines, pro-inflammatory cytokines, and mediators important in wound healing, e.g., IL-6, TNFalpha, IL-8, and RANTES. betulin 7-14 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 27104513-8 2016 Gallic acid and chlorogenic acid could suppress the release of pro-inflammatory cytokine IL-6 and chemokine CCL7 and CXCL8, respectively, in IL-31- and IL-33-treated eosinophils-dermal fibroblasts co-culture; while berberine could suppress the release of IL-6, CXCL8, CCL2 and CCL7 in the eosinophil culture and eosinophils-dermal fibroblasts co-culture (all p < 0.05). Gallic Acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 117-122 27104513-8 2016 Gallic acid and chlorogenic acid could suppress the release of pro-inflammatory cytokine IL-6 and chemokine CCL7 and CXCL8, respectively, in IL-31- and IL-33-treated eosinophils-dermal fibroblasts co-culture; while berberine could suppress the release of IL-6, CXCL8, CCL2 and CCL7 in the eosinophil culture and eosinophils-dermal fibroblasts co-culture (all p < 0.05). Gallic Acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 261-266 27104513-8 2016 Gallic acid and chlorogenic acid could suppress the release of pro-inflammatory cytokine IL-6 and chemokine CCL7 and CXCL8, respectively, in IL-31- and IL-33-treated eosinophils-dermal fibroblasts co-culture; while berberine could suppress the release of IL-6, CXCL8, CCL2 and CCL7 in the eosinophil culture and eosinophils-dermal fibroblasts co-culture (all p < 0.05). Chlorogenic Acid 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 117-122 27104513-8 2016 Gallic acid and chlorogenic acid could suppress the release of pro-inflammatory cytokine IL-6 and chemokine CCL7 and CXCL8, respectively, in IL-31- and IL-33-treated eosinophils-dermal fibroblasts co-culture; while berberine could suppress the release of IL-6, CXCL8, CCL2 and CCL7 in the eosinophil culture and eosinophils-dermal fibroblasts co-culture (all p < 0.05). Chlorogenic Acid 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 261-266 27091625-5 2016 Transcriptomic profiling revealed the up-regulation of three NF-kappaB-regulated CXC-chemokines, CXCL8, CXCL1 and CXCL2, in the resistant cells that were more efficiently down-regulated after OXA + Curcumin treatment as compared to the sensitive cells. Oxaliplatin 192-195 C-X-C motif chemokine ligand 8 Homo sapiens 97-102 27091625-6 2016 Moreover, CXCL8 and CXCL1 gene silencing made resistant cells more sensitive to OXA through the inhibition of the Akt/NF-kappaB pathway. Oxaliplatin 80-83 C-X-C motif chemokine ligand 8 Homo sapiens 10-15 26276563-11 2016 The results showed that the expression levels of IL-6, IL-8, TNF-alpha, and NF-kappaB which seemed to be a critical mediator in the inflammatory response tended to increase in the birds chronically treated with As2O3. Arsenic Trioxide 211-216 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 26975834-2 2016 Here, for the first time, we show that the coupling of hydrogen adsorption and absorption could trigger giant reversible strain in bulk nanoporous Pd (np-Pd) in a weakly adsorbed NaF electrolyte. Hydrogen 55-63 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 26975834-2 2016 Here, for the first time, we show that the coupling of hydrogen adsorption and absorption could trigger giant reversible strain in bulk nanoporous Pd (np-Pd) in a weakly adsorbed NaF electrolyte. Palladium 147-149 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 26893158-7 2016 However, 1,25-dihydroxyvitamin D3 exhibited superior anti-inflammatory effects as it furthermore reduced cytokine-induced NF-kappaB nuclear translocation and interleukin-8 mRNA stability and secretion. Calcitriol 9-33 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 27069129-0 2016 Unfractionated Heparin Selectively Modulates the Expression of CXCL8, CCL2 and CCL5 in Endometrial Carcinoma Cells. Heparin 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 63-68 27069129-5 2016 UFH attenuated the secretion of CXCL8 and CCL2, and enhanced that of CCL5. Heparin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 32-37 27069129-7 2016 CONCLUSION: UFH has selective modulating effects on the secretion of CXCL8, CCL2 and CCL5 in different endometrial adenocarcinoma cell lines. Heparin 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 69-74 27433050-16 2016 CONCLUSION: Subsequent to the use of NaF (0.05%) daily mouthrinse and MFP dentifrice (1000 ppm) the fluoride concentration in saliva remained elevated to a level of 0.12 ppm for mouthrinse and 0.14 ppm for dentifrice compared to baseline (0.03 ppm) up to 20 hrs postuse. Fluorides 100-108 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 26774572-5 2016 In addition, the anti-inflammatory properties of the modified Co-Cr surfaces were assessed by measuring IL-8 and IL-6 expression levels in human endothelial cell cultures. co-cr 62-67 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 26774572-7 2016 Interestingly, ASP- and PROP-containing substrates not only showed reduced adhesion of platelets and delayed coagulation time, but also drastically reduced the expression level of IL-8 and IL-6. Aspirin 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 26774572-7 2016 Interestingly, ASP- and PROP-containing substrates not only showed reduced adhesion of platelets and delayed coagulation time, but also drastically reduced the expression level of IL-8 and IL-6. Propolis 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 26934431-4 2016 CuONPs treatment caused a significant increase in IL-6 and IL-8 mRNA expression and protein levels in H292 cells in a concentration-dependent manner. cuonps 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 26071024-8 2016 In addition, adenosine-uridine-rich elements (AREs) of the CXCL8/IL-8 3"-untranslated region (3"-UTR) reduce CXCL8/IL-8 mRNA stability. adenosine-uridine 13-30 C-X-C motif chemokine ligand 8 Homo sapiens 59-64 26071024-8 2016 In addition, adenosine-uridine-rich elements (AREs) of the CXCL8/IL-8 3"-untranslated region (3"-UTR) reduce CXCL8/IL-8 mRNA stability. adenosine-uridine 13-30 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 26071024-8 2016 In addition, adenosine-uridine-rich elements (AREs) of the CXCL8/IL-8 3"-untranslated region (3"-UTR) reduce CXCL8/IL-8 mRNA stability. adenosine-uridine 13-30 C-X-C motif chemokine ligand 8 Homo sapiens 109-114 26071024-8 2016 In addition, adenosine-uridine-rich elements (AREs) of the CXCL8/IL-8 3"-untranslated region (3"-UTR) reduce CXCL8/IL-8 mRNA stability. adenosine-uridine 13-30 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 27135904-7 2016 Oral lansoprazole therapy decreased the frequency of acute exacerbation of COPD by alleviating gastroesophageal reflux and lowering the levels of IL-1beta, IL-6, IL-8, TNF-alpha and GM-CSF in the sputum. Lansoprazole 5-17 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 26658749-10 2016 Treatment of HUVECs with citral significantly inhibited TNF-alpha and IL-8 expression induced by LPS. citral 25-31 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 26921254-4 2016 Additionally,L-cys suppressed the LPS-induced intestinal inflammation and oxidative stress, as demonstrated by down-regulated TNF-alpha, IL-6 and IL-8 mRNA levels, increased catalase, superoxide dismutase, glutathione peroxidase activity, glutathione (GSH) contents and the ratio of GSH and oxidized glutathione in jejunum and ileum. Cysteine 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 26418512-2 2016 Nicotine is the most extensively investigated component of cigarette smoke, and a comprehensive analysis of the genes induced by nicotine stimulation revealed that interleukin-8 (IL-8) was induced in oral squamous cell carcinoma cell (OSCC). Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 164-177 26179980-5 2016 The results showed that exposure of monocytes to non-toxic doses of U-PM alone caused generation of reactive oxygen species (ROS), increased phosphorylation of p38, and activation of monocytes which was reflected by up-regulation of MMP-2, MMP-9 and proinflammatory cytokines IL-1beta and IL-8 expression and increased activity of pro-MMP-2 and pro-MMP-9. u-pm 68-72 C-X-C motif chemokine ligand 8 Homo sapiens 289-293 26418512-0 2016 Nicotine-Mediated Ca(2+)-Influx Induces IL-8 Secretion in Oral Squamous Cell Carcinoma Cell. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 26914908-14 2016 Nine women (60%) had L. crispatus detected post-DMPA, which significantly correlated with reduced IL-6 (P < 0.01) and IL-8 (P = 0.02). Medroxyprogesterone Acetate 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 26825457-5 2016 AZO significantly reduced TSLP levels as well as interleukin (IL)-6, IL-8, and tumor necrosis factor (TNF)-alpha without inducing cytotoxicity. anthrone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 26825457-6 2016 Furthermore, AZO more effectively reduced TSLP, IL-6, IL-8, and TNF-alpha levels than ZO-NP. anthrone 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 26418512-2 2016 Nicotine is the most extensively investigated component of cigarette smoke, and a comprehensive analysis of the genes induced by nicotine stimulation revealed that interleukin-8 (IL-8) was induced in oral squamous cell carcinoma cell (OSCC). Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 26418512-2 2016 Nicotine is the most extensively investigated component of cigarette smoke, and a comprehensive analysis of the genes induced by nicotine stimulation revealed that interleukin-8 (IL-8) was induced in oral squamous cell carcinoma cell (OSCC). Nicotine 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 164-177 26418512-2 2016 Nicotine is the most extensively investigated component of cigarette smoke, and a comprehensive analysis of the genes induced by nicotine stimulation revealed that interleukin-8 (IL-8) was induced in oral squamous cell carcinoma cell (OSCC). Nicotine 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 26418512-3 2016 Based on this background, the signaling mechanisms of nicotine-mediated IL-8 induction in OSCC was investigated. Nicotine 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 26418512-4 2016 Augmented IL-8 secretion by Ca9-22 cells was blocked by the NF-kappaB inhibitor L-1-4"-tosylamino-phenylethyl-chloromethyl ketone (TPCK) and the nicotinic acetylcholine receptor (nAChR)-specific inhibitor alpha-bungarotoxin (alphaBtx). Tosylphenylalanyl Chloromethyl Ketone 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 26418512-6 2016 Only the CaMK II inhibitor was found to exert an inhibitory effect on nicotine-mediated IL-8 secretion. Nicotine 70-78 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 26418512-7 2016 Pre-treatment of the Ca9-22 cells with the Ca(2+) chelator BAPTA-AM drastically inhibited IL-8 secretion. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 59-67 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 26418512-11 2016 Nicotine-mediated IL-8 induction should be a trigger for the initiation of various diseases. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 26332444-8 2016 NODs agonist, Tri-DAP and MDP, led to the production of IL-8 and MAPK activation. L-Ala-gamma-D-Glu-meso-diaminopimelic acid 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 26332444-8 2016 NODs agonist, Tri-DAP and MDP, led to the production of IL-8 and MAPK activation. Acetylmuramyl-Alanyl-Isoglutamine 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 26687822-10 2016 Blocking of ERK, SAPK/JNK, and p38 MAPK inhibited the CTS-induced stimulation of COX-2 and IL-8, while IL-6 expression was mediated only by SAPK/JNK and p38 MAPK. castanospermine 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 26780941-0 2016 MEK activity controls IL-8 expression in tamoxifen-resistant MCF-7 breast cancer cells. Tamoxifen 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 26780941-2 2016 In the present study, we investigated the possibility that interleukin-8 (IL-8) is a prognostic marker for tamoxifen resistance and aimed to clarify the regulation of IL-8 expression in tamoxifen-resistant cells. Tamoxifen 107-116 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 26780941-2 2016 In the present study, we investigated the possibility that interleukin-8 (IL-8) is a prognostic marker for tamoxifen resistance and aimed to clarify the regulation of IL-8 expression in tamoxifen-resistant cells. Tamoxifen 186-195 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 26780941-4 2016 In addition, the levels of IL-8 mRNA and protein expression were significantly increased in tamoxifen-resistant (TamR) cells compared to tamoxifen-sensitive (TamS) cells. Tamoxifen 92-101 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 26780941-4 2016 In addition, the levels of IL-8 mRNA and protein expression were significantly increased in tamoxifen-resistant (TamR) cells compared to tamoxifen-sensitive (TamS) cells. tamr 113-117 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 26780941-4 2016 In addition, the levels of IL-8 mRNA and protein expression were significantly increased in tamoxifen-resistant (TamR) cells compared to tamoxifen-sensitive (TamS) cells. Tamoxifen 137-146 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 26780941-4 2016 In addition, the levels of IL-8 mRNA and protein expression were significantly increased in tamoxifen-resistant (TamR) cells compared to tamoxifen-sensitive (TamS) cells. tams 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 26537370-8 2016 RESULTS: High glucose levels inhibited PDLSC proliferation and differentiation into osteoblasts but induced NF-kappaB activation and subsequent interleukin (IL)-6 and IL-8 expression. Glucose 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 26975648-5 2016 Furthermore, methylglyoxal induced carbonyl stress promotes the expression of the pro-inflammatory interleukins IL-6 and IL-8. Pyruvaldehyde 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 26990318-8 2016 At 90 min, the nVNS group had a greater percent decrease in IL-8 concentration (p < 0.05) compared to SST group. nvns 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 26780941-7 2016 On the contrary, we observed that elevated IL-8 mRNA expression was suppressed by a specific MEK1/2 inhibitor, UO126, but not by the specific PI-3K inhibitor LY294002, in TamR cells, whereas, we found that overexpression of constitutively active-MEK (CA-MEK) significantly increased the levels of IL-8 mRNA expression in TamS cells. U 0126 111-116 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 26811545-9 2016 Concordantly, the ERK inhibitor U0126 significantly decreased IL1B-induced IL6, CXCL8, CCL2 and PTGS2 mRNA abundance; IL6, CXCL8, CCL2 and PGF2 alpha release; and NF-kappaB activation. U 0126 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 26780941-9 2016 Taken together, our results demonstrate that IL-8 expression is regulated through a MEK/ERK-dependent pathway in TamR cells, suggesting that IL-8 and its receptors may be promising therapeutic targets for overcoming tamoxifen resistance. Tamoxifen 216-225 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 26780941-9 2016 Taken together, our results demonstrate that IL-8 expression is regulated through a MEK/ERK-dependent pathway in TamR cells, suggesting that IL-8 and its receptors may be promising therapeutic targets for overcoming tamoxifen resistance. Tamoxifen 216-225 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 26504904-6 2016 Patients who had higher levels of IL-1beta and IL-8 were more responsive to topical sulfasalazine therapy. Sulfasalazine 84-97 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 26504904-8 2016 Furthermore, high concentrations of IL-1beta and IL-8 in the saliva are useful indicators for the application of topical sulfasalazine in OLP patients refractory to steroid treatment. Sulfasalazine 121-134 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 26811545-9 2016 Concordantly, the ERK inhibitor U0126 significantly decreased IL1B-induced IL6, CXCL8, CCL2 and PTGS2 mRNA abundance; IL6, CXCL8, CCL2 and PGF2 alpha release; and NF-kappaB activation. U 0126 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 26503211-8 2016 Multivariate Cox regression analysis identified IL-8 as an independent adverse prognostic factor of CSS (P < 0.001) and RFS (P < 0.001), which could be incorporated into the traditional TNM staging system to improve the prognostic value for CSS and RFS in ccRCC patients. thiocysteine 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 26537583-6 2016 We observed that elevated IL-8 mRNA expression and protein secretion were suppressed by a specific MEK1/2 inhibitor, UO126. U 0126 117-122 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 26503211-8 2016 Multivariate Cox regression analysis identified IL-8 as an independent adverse prognostic factor of CSS (P < 0.001) and RFS (P < 0.001), which could be incorporated into the traditional TNM staging system to improve the prognostic value for CSS and RFS in ccRCC patients. thiocysteine 247-250 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 26503211-10 2016 Increased expression of IL-8 is a potential independent adverse prognostic biomarker for CSS and RFS in patients with ccRCC after nephrectomy. thiocysteine 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 27011164-7 2016 The ER stress inhibitor salubrinal repressed, but inducer tunicamycin enhanced, the production of IL-6, IL-8, MMP-8, and MMP-9 in hPDLCs. salubrinal 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 27076279-1 2016 A sensitive and convenient electrochemical method was developed for the determination of rhodamine B by a silica-pillared zirconium phosphate/nafion composite (SPZP/NAF) modified glassy carbon electrode. rhodamine B 89-100 C-X-C motif chemokine ligand 8 Homo sapiens 165-168 27076279-1 2016 A sensitive and convenient electrochemical method was developed for the determination of rhodamine B by a silica-pillared zirconium phosphate/nafion composite (SPZP/NAF) modified glassy carbon electrode. Silicon Dioxide 106-112 C-X-C motif chemokine ligand 8 Homo sapiens 165-168 27076279-3 2016 Because of the layer structure and large specific surface area of SPZP, the SPZP/NAF modified glassy carbon electrode showed high electrocatalytic activity toward the oxidation of rhodamine B. spzp 66-70 C-X-C motif chemokine ligand 8 Homo sapiens 76-84 27076279-3 2016 Because of the layer structure and large specific surface area of SPZP, the SPZP/NAF modified glassy carbon electrode showed high electrocatalytic activity toward the oxidation of rhodamine B. Carbon 101-107 C-X-C motif chemokine ligand 8 Homo sapiens 76-84 27076279-3 2016 Because of the layer structure and large specific surface area of SPZP, the SPZP/NAF modified glassy carbon electrode showed high electrocatalytic activity toward the oxidation of rhodamine B. rhodamine B 180-191 C-X-C motif chemokine ligand 8 Homo sapiens 76-84 27076279-4 2016 Under optimal experimental conditions, the SPZP/NAF modified electrode exhibited a wide linear response to rhodamine B ranging from 0.01 to 5.0 muM and a low detection limit down to 4.3 nM (S/N = 3). spzp 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 27076279-4 2016 Under optimal experimental conditions, the SPZP/NAF modified electrode exhibited a wide linear response to rhodamine B ranging from 0.01 to 5.0 muM and a low detection limit down to 4.3 nM (S/N = 3). rhodamine B 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 26956674-7 2016 RESULTS: ASM cell migration toward CSE-stimulated A549 cells was markedly reduced by Ac-RRWWCR-NH2 (IL-8 inhibitor) and SB431542 (TGF-beta1 inhibitor). antileukinate 85-98 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 26803523-7 2016 The results showed that acanthoic acid dose-dependently inhibited LPS-induced TNF-alpha and IL-8 production. acanthoic acid 24-38 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 25589513-10 2016 RESULTS: Butyrate decreased C16.0+MSU-induced production of IL-1beta, IL-6, IL-8 and IL-1beta mRNA in PBMCs from healthy donors. Butyrates 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 26695197-9 2016 The decrease in glucose observed for serum and NaF/KOx tubes was clinically significant at all specified time points while the bias for Glucomedics tubes did not exceed the criteria even with a centrifugation delay of 180 min. Glucose 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 26803523-8 2016 Acanthoic acid also inhibited TNF-alpha-induced IL-8 and IL-6 production. acanthoic acid 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 28390210-7 2016 The reference toothpaste contained 927 ppm fluoride as NaF in a conventional amorphous silica abrasive base. Fluorides 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 26370214-8 2016 MWCNTs-COOH induced interleukin-6 (IL-6) and IL-8 release in A549 cells whereas p-MWCNTs induced IL-8 release in BEAS-2B cells. Carbonic Acid 7-11 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 26609182-5 2016 We previously developed a (99m)Tc-labeled CXCL8 preparation in preclinical models including colitis and clinical studies. Technetium 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 42-47 26908203-0 2016 Induction of IL-8(CXCL8) and MCP-1(CCL2) with oxidative stress and its inhibition with N-acetyl cysteine (NAC) in cell culture model using HK-2 cell. Acetylcysteine 87-104 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 26706024-6 2016 Glutamine supplementation significantly (P < 0.05) attenuated the release of IL-10 at 4 h and IL-8 at 24 h, compared with conditions without glutamine. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 26786756-9 2016 CONCLUSIONS: The present study suggests that controlled exposure to Al2O3 particles at levels below PEL (TWA) induces airway inflammation in healthy humans marked by elevated neutrophils and elevated IL-8. Aluminum Oxide 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 26926362-0 2016 Prostaglandin E2 possesses different potencies in inducing Vascular Endothelial Growth Factor and Interleukin-8 production in COPD human lung fibroblasts. Dinoprostone 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 26926362-1 2016 We studied the role of PGE2, its biosynthetic enzymes and its receptors, in regulating the functions of lung fibroblasts through the production of Vascular Endothelial Growth Factor (VEGF) and Interleukin-8 (IL-8) in COPD subjects. Dinoprostone 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 193-206 26926362-1 2016 We studied the role of PGE2, its biosynthetic enzymes and its receptors, in regulating the functions of lung fibroblasts through the production of Vascular Endothelial Growth Factor (VEGF) and Interleukin-8 (IL-8) in COPD subjects. Dinoprostone 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 26926362-6 2016 Low concentrations of synthetic PGE2 increased the release of VEGF in HFL-1, but higher concentrations were needed to induce the release of IL-8. Dinoprostone 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 26926362-8 2016 In the airways of COPD subjects, fibroblast-derived PGE2 may regulate angiogenesis and inflammation through the production of VEGF and IL-8 respectively, suggesting that the increase in expression of COX-2, EP2 and EP4 observed in COPD fibroblasts may contribute to steering the role of PGE2 from homeostatic to pro-inflammatory. Dinoprostone 52-56 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 24193047-4 2016 Therefore, in this study, we investigated the effects of sodium fluoride (NaF) and/or lead acetate (PbAc) on development of apoptosis, cell vitality, and proliferation in the liver cell line HepG2. Sodium Fluoride 57-72 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 24193047-6 2016 Incubation of the hepatocytes with NaF or PbAc increased apoptosis, more when fluoride and Pb were used simultaneously. Fluorides 78-86 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 26908203-0 2016 Induction of IL-8(CXCL8) and MCP-1(CCL2) with oxidative stress and its inhibition with N-acetyl cysteine (NAC) in cell culture model using HK-2 cell. Acetylcysteine 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 26908203-9 2016 Exposure to hydrogen peroxide induced a significant increase in the activity of the antioxidant enzyme glutathione peroxidase and the levels of the chemokines Interleukin-8 (IL-8; CXCL8) and MCP-1 (CCL2). Hydrogen Peroxide 12-29 C-X-C motif chemokine ligand 8 Homo sapiens 159-172 26908203-9 2016 Exposure to hydrogen peroxide induced a significant increase in the activity of the antioxidant enzyme glutathione peroxidase and the levels of the chemokines Interleukin-8 (IL-8; CXCL8) and MCP-1 (CCL2). Hydrogen Peroxide 12-29 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 26908203-9 2016 Exposure to hydrogen peroxide induced a significant increase in the activity of the antioxidant enzyme glutathione peroxidase and the levels of the chemokines Interleukin-8 (IL-8; CXCL8) and MCP-1 (CCL2). Hydrogen Peroxide 12-29 C-X-C motif chemokine ligand 8 Homo sapiens 180-185 26908203-11 2016 The cytokine Interleukin-1beta (IL-1beta) at 1 ng/ml significantly potentiated the expression of both IL-8 (CXCL8) and MCP-1 (CCL2) which showed synergistic response in the presence of hydrogen peroxide. Hydrogen Peroxide 185-202 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 26908203-11 2016 The cytokine Interleukin-1beta (IL-1beta) at 1 ng/ml significantly potentiated the expression of both IL-8 (CXCL8) and MCP-1 (CCL2) which showed synergistic response in the presence of hydrogen peroxide. Hydrogen Peroxide 185-202 C-X-C motif chemokine ligand 8 Homo sapiens 108-113 26908203-12 2016 Pre-incubation of the cells with the anti-oxidant N-acetyl cysteine (NAC) strongly suppressed the induction of both IL-8 and MCP-1 when stimulated with hydrogen peroxide and IL-1beta. Acetylcysteine 50-67 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26908203-12 2016 Pre-incubation of the cells with the anti-oxidant N-acetyl cysteine (NAC) strongly suppressed the induction of both IL-8 and MCP-1 when stimulated with hydrogen peroxide and IL-1beta. Acetylcysteine 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26908203-12 2016 Pre-incubation of the cells with the anti-oxidant N-acetyl cysteine (NAC) strongly suppressed the induction of both IL-8 and MCP-1 when stimulated with hydrogen peroxide and IL-1beta. Hydrogen Peroxide 152-169 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26840091-7 2016 This study shows that a monoclonal anti-TLR4 antibody inhibited cobalt-mediated increases in pro-inflammatory IL8, CCL20 and IL1A expression, as well as IL-8 secretion. Cobalt 64-70 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 27212782-2 2016 It has been recently shown that active microcalcification in the coronary arteries, one of the features that characterizes vulnerable plaques at risk of rupture, can be imaged using cardiac gated 18F-sodium fluoride (18F-NaF) PET. 18f-sodium fluoride 196-215 C-X-C motif chemokine ligand 8 Homo sapiens 221-224 26721883-7 2016 One domain, consisting of N-loop and C-helical residues (defined as alpha-domain) has also been identified previously as the GAG-binding domain for the related chemokine CXCL8/IL-8. Glycosaminoglycans 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 170-175 26721883-7 2016 One domain, consisting of N-loop and C-helical residues (defined as alpha-domain) has also been identified previously as the GAG-binding domain for the related chemokine CXCL8/IL-8. Glycosaminoglycans 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 26846189-2 2016 Here, we successfully demonstrate the novel use of zinc oxide nanorods (ZnO NRs) in the ultrasensitive and quantitative detection of two acute kidney injury (AKI)-related protein biomarkers, tumor necrosis factor (TNF)-alpha and interleukin (IL)-8, directly from patient samples. Zinc Oxide 51-61 C-X-C motif chemokine ligand 8 Homo sapiens 229-247 26846189-2 2016 Here, we successfully demonstrate the novel use of zinc oxide nanorods (ZnO NRs) in the ultrasensitive and quantitative detection of two acute kidney injury (AKI)-related protein biomarkers, tumor necrosis factor (TNF)-alpha and interleukin (IL)-8, directly from patient samples. Zinc Oxide 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 229-247 26846189-3 2016 We first validate the ZnO NRs-based IL-8 results via comparison with those obtained from using a conventional enzyme-linked immunosorbent method in samples from 38 individuals. Zinc Oxide 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 26719146-8 2016 Stimulation of BEAS-2B cells with supernatant of CS-induced necrotic cells induced a significant increase in the release of CXCL8 and IL-6, in a myeloid differentiation primary response gene 88-dependent fashion. Cesium 49-51 C-X-C motif chemokine ligand 8 Homo sapiens 124-129 26857501-7 2016 In high, non-toxic concentrations all transition metals except Cr induced IL-8 and IL-6 production in microglia, with Ni and Co providing the strongest stimulation. Chromium 63-65 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 26857501-8 2016 When using near-physiological doses (up to 10x the normal plasma concentration), only Zn and Cu induced significant IL-8 production. Zinc 86-88 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26857501-8 2016 When using near-physiological doses (up to 10x the normal plasma concentration), only Zn and Cu induced significant IL-8 production. Copper 93-95 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26611525-9 2016 Aspect of patients, 0.45% NaCl group and 0.9% NaCl+ambroxol group were significantly different in the levels of SP-A, IL-6, IL-8 and TNF-alpha (P<0.01). Sodium Chloride 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 26611525-9 2016 Aspect of patients, 0.45% NaCl group and 0.9% NaCl+ambroxol group were significantly different in the levels of SP-A, IL-6, IL-8 and TNF-alpha (P<0.01). Sodium Chloride 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 26848751-9 2016 These results show that EGCG suppresses the IL-1beta-induced expression of IL-8 through inhibition of the NF-kappaB, p38, and ERK pathways. epigallocatechin gallate 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 26848751-0 2016 The Effect of (-)-Epigallocatechin-3-Gallate on IL-1beta Induced IL-8 Expression in Orbital Fibroblast from Patients with Thyroid-Associated Ophthalmopathy. epigallocatechin gallate 14-44 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 26859301-5 2016 Both higher serum IL-8 (95% CI = 0.10,3.84) and poor sleep (95% CI = 0.03,0.28) served as significant mediators linking lower DHA:AA ratios with shorter gestation. Docosahexaenoic Acids 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 26859301-6 2016 Further, a serial mediation model moving from the DHA:AA ratio sleep IL-8 length of gestation was statistically significant (95% CI = 0.02, 0.79). Docosahexaenoic Acids 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 26861339-5 2016 In comparison, sIPNs containing 300% w/w linear polymer showed an average area reduction of ~45% when the temperature was raised from 20 C to 70 C, ~36% when immersed in 1% NaF w/w salt solution and ~10% after 30 min exposure to white light irradiation, respectively. sipns 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 26861339-5 2016 In comparison, sIPNs containing 300% w/w linear polymer showed an average area reduction of ~45% when the temperature was raised from 20 C to 70 C, ~36% when immersed in 1% NaF w/w salt solution and ~10% after 30 min exposure to white light irradiation, respectively. Polymers 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 26861339-5 2016 In comparison, sIPNs containing 300% w/w linear polymer showed an average area reduction of ~45% when the temperature was raised from 20 C to 70 C, ~36% when immersed in 1% NaF w/w salt solution and ~10% after 30 min exposure to white light irradiation, respectively. Salts 183-187 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 26848751-5 2016 Treatment with EGCG significantly reduced the level of IL-1beta-induced secretion of IL-8 and the expression of IL-8 mRNA. epigallocatechin gallate 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 26848751-5 2016 Treatment with EGCG significantly reduced the level of IL-1beta-induced secretion of IL-8 and the expression of IL-8 mRNA. epigallocatechin gallate 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 26870616-4 2016 Our results revealed that the wound healing induced by CXCL8 was greatly attenuated by removal of HS. Heparitin Sulfate 98-100 C-X-C motif chemokine ligand 8 Homo sapiens 55-60 26848751-6 2016 IL-1beta-induced the degradation of IkappaBalpha, and the phosphorylation of p38 and ERK, and the IL-1beta-induced expression of IL-8 mRNA was inhibited by specific inhibitors, such as BAY-117085 for NF-kB, SB203580 for p38, and PD98059 for ERK. BAY 11-7085 185-195 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 26848751-6 2016 IL-1beta-induced the degradation of IkappaBalpha, and the phosphorylation of p38 and ERK, and the IL-1beta-induced expression of IL-8 mRNA was inhibited by specific inhibitors, such as BAY-117085 for NF-kB, SB203580 for p38, and PD98059 for ERK. SB 203580 207-215 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 26848751-6 2016 IL-1beta-induced the degradation of IkappaBalpha, and the phosphorylation of p38 and ERK, and the IL-1beta-induced expression of IL-8 mRNA was inhibited by specific inhibitors, such as BAY-117085 for NF-kB, SB203580 for p38, and PD98059 for ERK. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 229-236 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 26870616-0 2016 Role of heparan sulfate in mediating CXCL8-induced endothelial cell migration. Heparitin Sulfate 8-23 C-X-C motif chemokine ligand 8 Homo sapiens 37-42 26870616-7 2016 Taken together, our results demonstrated an essential role of HS in mediating CXCL8-induced endothelial cell migration, and highlighted the biological importance of the interaction between CXCL8 and heparan sulfate in wound healing. Heparitin Sulfate 62-64 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 26870616-7 2016 Taken together, our results demonstrated an essential role of HS in mediating CXCL8-induced endothelial cell migration, and highlighted the biological importance of the interaction between CXCL8 and heparan sulfate in wound healing. Heparitin Sulfate 199-214 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 26615574-0 2016 Farrerol inhibits IL-6 and IL-8 production in LPS-stimulated human gingival fibroblasts by suppressing PI3K/AKT/NF-kappaB signaling pathway. farrerol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 26615574-2 2016 In the present study, we investigated the anti-inflammatory effects of farrerol on the production of IL-6 and IL-8 in human gingival fibroblasts (HGFs) treated with lipopolysaccharide (LPS). farrerol 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 26615574-6 2016 RESULTS: These results showed that farrerol inhibited LPS-induced IL-6 and IL-8 production in a dose dependent manner. farrerol 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 26603163-10 2016 The Interleukin 8-251A > T SNP was significantly correlated with an increased tumor (p = 0.048), PTE (p = 0.033) and necrosis volume (p = 0.028). pte 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 4-17 26615574-9 2016 CONCLUSION: These results indicated that farrerol attenuated IL-6 and IL-8 production by inhibition of PI3K and AKT phosphorylation, resulting in an inhibition of NF-kappaB activation. farrerol 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 26136303-15 2016 The replacement of NaF/KOx with Glucomedics tubes substantially impacts glucose results, giving marked rise in diabetes prevalence. Glucose 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 26387832-5 2016 Our results were analogous to previous reports in that Meth up-regulates TNF-alpha and IL-8 after two hours of exposure. Methamphetamine 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 26677054-8 2016 Treating A549 cells with either EtOH or EtP significantly reduced the IL-1beta- or TNF-induced IL-8 release, whereas treating Huh7 cells did not significantly alter IL-6 release. Ethanol 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 26677054-8 2016 Treating A549 cells with either EtOH or EtP significantly reduced the IL-1beta- or TNF-induced IL-8 release, whereas treating Huh7 cells did not significantly alter IL-6 release. ethyl pyruvate 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 26212931-6 2016 Remarkably, reduction of DG levels using the phosphatidylcholine-specific phospholipase C inhibitor D609 inhibited the secretion of VEGF and Angiopoietin-2, but increased the secretion of interleukin-8, without affecting significantly their respective mRNA levels. Phosphatidylcholines 45-64 C-X-C motif chemokine ligand 8 Homo sapiens 188-201 26212931-6 2016 Remarkably, reduction of DG levels using the phosphatidylcholine-specific phospholipase C inhibitor D609 inhibited the secretion of VEGF and Angiopoietin-2, but increased the secretion of interleukin-8, without affecting significantly their respective mRNA levels. tricyclodecane-9-yl-xanthogenate 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 188-201 26136303-8 2016 The regression equation obtained comparing citrate to NaF/KOx tubes was used to recalculate glucose results retrieved from the laboratory information system. Glucose 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 26136303-9 2016 RESULTS: Glucose measured in Glucomedics was higher (9.9%; p<0.001), while glucose in NaF/KOx and serum was lower compared to LiH (2.4%; p<0.001 and 3.2%; p<0.001, respectively). Glucose 78-85 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 26501345-8 2016 Alcohol ingestion after resistance exercise affected aspects of inflammatory capacity (IL-6 and IL-8 production). Alcohols 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 26329367-0 2016 Veratric Acid Inhibits LPS-Induced IL-6 and IL-8 Production in Human Gingival Fibroblasts. veratric acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 26329367-6 2016 The results showed that veratric acid inhibited LPS-induced IL-6 and IL-8 production, as well as iNOS and COX-2 expression. veratric acid 24-37 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 26378248-8 2016 Messenger RNA and protein levels of the inflammatory marker, interleukin-8, also increased following exposure to indium release ITO. Indium 113-119 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 25610950-5 2016 RESULTS: We found that BP IgG-induced IL-6 and IL-8 release from HaCaT cells was reduced in the presence of non-toxic doses of calcitriol. Calcitriol 127-137 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 26893718-8 2016 Furthermore, IA (0.1-10 micromol/l) significantly inhibited PGE2 production and COX2 expression in cells with LPS-induced IL-8, in a concentration-dependent manner. Dinoprostone 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 26701795-10 2016 GOS reduced TNF-alpha- and IL-1beta-induced inflammatory responses to 25-26% and pathogen-induced IL-8 and MCP-1 to 36-39% of positive controls (P < 0.001). D-Glucitol-1,6-bisphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 26553025-10 2016 However, a trend toward decreased IL-6, IL-8, and IFN-gamma levels, and favorable clinical outcomes were present in the macrolide group. Macrolides 120-129 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 26359174-6 2016 RESULTS: Beyond the factors included in the definition, SLE patients with MetS have a significantly higher serum level of uric acid (6.88 +- 2.20 vs 4.45 +- 1.17, p < 0.001) and some inflammatory biomarkers such as homocysteine, IL-8, sICAM-1 or complement molecules. Uric Acid 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 26334623-7 2016 Upon MC-A treatment, hMSCs decreased the expression levels of various cytokines including TNF-alpha, VEGF, IL-6, IL-8 and FGF-2. myrtucommulone A 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 26871861-9 2016 HE and MT staining showed that the cartilage defect sites of the group receiving the combination of IL-8 and BMC were regenerated with cartilage-like tissues showing chondrocyte morphology. Helium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 26871861-9 2016 HE and MT staining showed that the cartilage defect sites of the group receiving the combination of IL-8 and BMC were regenerated with cartilage-like tissues showing chondrocyte morphology. Meitnerium 7-9 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 26814891-5 2016 Women using injectable DMPA had increased concentration of several soluble proteins of the innate and adaptive immune system, including IL-1alpha, IL-1beta, IL-2, MIP-1beta, IP-10, IL-8, TGF-beta, HBD4, IgA, IgG1, and IgG2. N,N-dimethyl-4-anisidine 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 26871861-10 2016 Safranin O staining showed hyaline cartilage regeneration in the group receiving IL-8 and BMC, whereas fibrous-like tissues were formed in the other groups. phenosafranine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 27078994-9 2016 Compared with the HSP group, levels of IL-8, TNF-alpha, and NO significantly decreased after intervention of TFB (1.0 and 0.5 mg/mL; P < 0.05, P < 0.01). tfb 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 27078994-12 2016 CONCLUSION: TFB could protect vascular damage by inhibiting in vivo high expression of NF-kappaB, reducing the production of IL-8, TNF-alpha, and NO in vascular endothelial cells of HSP children patients. tfb 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 26834946-1 2016 AIM: To investigating the relationship between thoracic and cardiac (18)F-Natrium-Fluoride (18F-NaF) uptake, as a marker of ongoing calcification and cardiovascular risk factors. Sodium Fluoride 74-90 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 26808546-10 2016 Among all patients, elevated levels of interleukin-8 (IL-8), carcinoembryonic antigen (CEA), hypoxia-inducible factor 1-alpha (HIF-1 alpha), and interleukin-6 were independently associated with lower OS, while IL-8, CEA, platelet-derived growth factor receptor alpha and mucin-1 were associated with metastatic disease. Osmium 200-202 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 26546780-7 2016 The expression of interleukin-8 (IL-8) in HL-60 cells treated with conditioned media from HepaRG cells (HL-60/HepaRG) exhibited the highest ROC-AUC value of 0.758, followed by the expression of IL-1beta in HL-60/HepaRG (ROC-AUC: 0.726). heparg 90-96 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 26546780-7 2016 The expression of interleukin-8 (IL-8) in HL-60 cells treated with conditioned media from HepaRG cells (HL-60/HepaRG) exhibited the highest ROC-AUC value of 0.758, followed by the expression of IL-1beta in HL-60/HepaRG (ROC-AUC: 0.726). heparg 90-96 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 26789270-7 2016 Tbeta4 activation with a Tbeta4 peptide attenuated the H2O2-induced production of NO and PGE2 and up-regulated iNOS, COX-2, and osteoclastogenic cytokines (TNF-alpha, IL-1beta, IL-6, IL-8, and IL-17) as well as reversed the effect on RANKL and OPG in PDLCs. Hydrogen Peroxide 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 26949603-7 2016 RESULTS: Triptolide inhibited the zymosan-induced release of IL-6, IL-8, and MCP-1 from HCFs in a concentration- and time-dependent manner. triptolide 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26589477-7 2016 Interestingly, poly(I:C), but neither lipopolysaccharide nor R848, increased IL-8 and chemokine (C-C motif) ligand 5 secretion. poly 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 77-116 26781963-7 2016 We found that accumulation of cholesterol was essential for IL-17A signaling as reduced total cholesterol levels by methyl beta cyclodextrin (MBCD), significantly decreased IL-17A induced secretion of CCL20, IL-8 and S100A7 from the keratinocytes. Cholesterol 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 26949603-7 2016 RESULTS: Triptolide inhibited the zymosan-induced release of IL-6, IL-8, and MCP-1 from HCFs in a concentration- and time-dependent manner. Zymosan 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26609552-8 2016 The inhibition efficiency of sodium fluoride (NaF) also received good results in pyrophosphatase inhibitor screening research. Sodium Fluoride 29-44 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 26762579-8 2016 Plasma concentrations of VEGFA, FLT3L, c-MET, AXL, Gas6A, bone-specific alkaline phosphatase, interleukin-8 and the hypoxia markers CA9 and clusterin significantly increased during treatment with cabozantinib irrespective of response. cabozantinib 196-208 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 26759169-8 2016 However, MSC pretreatment with cisplatin led to changes in phosphorylation profiles of many kinases and also increased secretion of IL-6 and IL-8 cytokines. Cisplatin 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 26747811-1 2016 The ionic stochastic motions in the molten alkali halide NaF are investigated by quasielastic neutron scattering and first principles molecular dynamics simulation. Alkalies 43-49 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 26747811-1 2016 The ionic stochastic motions in the molten alkali halide NaF are investigated by quasielastic neutron scattering and first principles molecular dynamics simulation. halide 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 26727989-1 2016 It was the aim of this study to investigate differences in fluoride bioavailability in different oral areas after the application of amine fluoride (AmF) and sodium fluoride (NaF). Fluorides 59-67 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 26727989-1 2016 It was the aim of this study to investigate differences in fluoride bioavailability in different oral areas after the application of amine fluoride (AmF) and sodium fluoride (NaF). Sodium Fluoride 158-173 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 26727989-8 2016 In the tongue coating, fluoride concentration increased faster after NaF application than after AmF application. Fluorides 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 26727989-9 2016 After 30 minutes, the fluoride concentration decreased and remained stable until 120 minutes after AmF application and returned to baseline after NaF application. Fluorides 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 26987326-3 2016 The present study was performed to assess the correlation between concentrations of IL-1beta, IL-6, IL-8, and TGF-beta1 in the serum with response to clarithromycin (CAM) treatment in patients with COP. Clarithromycin 150-164 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 26987326-9 2016 We conclude that IL-6, IL-8, and TGF-beta1 may play a role in the pathogenesis of COP, as their decreased concentrations were associated with a positive response to CAM treatment. Clarithromycin 165-168 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 26986079-2 2016 Sodium fluoride (NaF) has previously been shown to inhibit recombinant MMP-2 and MMP-9. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 26867523-4 2016 METHODS: The in vitro effects of AG1478 treatment of cultured NCI-H292 cells on lipopolysaccharide (LPS) induced or tumor necrosis factor (TNF) alpha induced MUC5AC mucin and IL-8 secretion were evaluated. RTKI cpd 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 27251500-5 2016 In addition, ferulic acid and kaempferol showed inhibition against interleukin-8 (IL-8) and interleukin-1beta (IL-1beta) expression while ferulic acid and caffeic acid showed comparatively higher inhibition of ED associated tumor necrosis factor-alpha (TNF-alpha) expression. ferulic acid 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 27251500-5 2016 In addition, ferulic acid and kaempferol showed inhibition against interleukin-8 (IL-8) and interleukin-1beta (IL-1beta) expression while ferulic acid and caffeic acid showed comparatively higher inhibition of ED associated tumor necrosis factor-alpha (TNF-alpha) expression. ferulic acid 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 27251500-5 2016 In addition, ferulic acid and kaempferol showed inhibition against interleukin-8 (IL-8) and interleukin-1beta (IL-1beta) expression while ferulic acid and caffeic acid showed comparatively higher inhibition of ED associated tumor necrosis factor-alpha (TNF-alpha) expression. kaempferol 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 27251500-5 2016 In addition, ferulic acid and kaempferol showed inhibition against interleukin-8 (IL-8) and interleukin-1beta (IL-1beta) expression while ferulic acid and caffeic acid showed comparatively higher inhibition of ED associated tumor necrosis factor-alpha (TNF-alpha) expression. kaempferol 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 27080946-0 2016 Tanshinone IIA Induces Heme Oxygenase 1 Expression and Inhibits Cyclic Strain-Induced Interleukin 8 Expression in Vascular Endothelial Cells. tanshinone 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 27080946-6 2016 HO-1 silencing significantly abrogated the repressive effects of tanshinone IIA on strain-induced IL-8 expression, which suggests HO-1 has a role in mediating the effects of tanshinone IIA. tanshinone 65-75 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 27080946-6 2016 HO-1 silencing significantly abrogated the repressive effects of tanshinone IIA on strain-induced IL-8 expression, which suggests HO-1 has a role in mediating the effects of tanshinone IIA. tanshinone 65-79 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 27080946-7 2016 This study reports for the first time that tanshinone IIA inhibits cyclic strain-induced IL-8 expression via the induction of HO-1 in endothelial cells, providing valuable new insight into the molecular pathways that may contribute to the effects of tanshinone IIA. tanshinone 43-53 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 27080946-7 2016 This study reports for the first time that tanshinone IIA inhibits cyclic strain-induced IL-8 expression via the induction of HO-1 in endothelial cells, providing valuable new insight into the molecular pathways that may contribute to the effects of tanshinone IIA. tanshinone 250-260 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 26353790-10 2016 In PsA explant, tofacitinib significantly decreased spontaneous secretion of IL-6, IL-8, MCP-1, MMP9/MMP2, MMP3 (all p<0.05) and decreased the MMP3/TIMP3 ratio (p<0.05), with no effect observed for IP-10 or IL-10. tofacitinib 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 27833438-0 2016 The inhibitory effect of flavonoids on interleukin-8 release by human gastric adenocarcinoma (AGS) cells infected with cag PAI (+) Helicobacter pylori. Flavonoids 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 26982743-10 2016 Both the B2 receptor antagonist MEN16132 and TLR-2 silencing inhibited IL-6 and IL-8 secretion in human OA synoviocytes. (4-amino-5-(4-(4-(2,4-dichloro-3-(2,4-dimethyl-8-quinolyloxymethyl)phenylsulfonamido)tetrahydro-2H-4-pyranoylcarbonyl)piperazino)-5-oxopentyl)(trimethyl)ammonium 32-40 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 27889767-8 2016 RESULTS: Upon Lipopolysaccharide (LPS)-induced inflammatory response in HUVECs, Crocetin ameliorated cell cytotoxicity, suppressed MCP-1 and IL-8 expressions through blocking NF-kappaB p65 signaling transduction. crocetin 80-88 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 27833443-12 2016 The cutoff value for detection of inflammatory changes in the DMSA scan for IL-8 was 120 pg/mg creatinine (Cr) and 40 pg/mg Cr for TGF-beta1. Succimer 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 27833443-12 2016 The cutoff value for detection of inflammatory changes in the DMSA scan for IL-8 was 120 pg/mg creatinine (Cr) and 40 pg/mg Cr for TGF-beta1. Creatinine 95-105 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 27833443-12 2016 The cutoff value for detection of inflammatory changes in the DMSA scan for IL-8 was 120 pg/mg creatinine (Cr) and 40 pg/mg Cr for TGF-beta1. Creatinine 107-109 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 26459323-4 2016 The overproduction of serum IL8 level was most significant in the CADM group with active period. cadm 66-70 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 27156328-0 2016 Glucose Stability Study: NaF/Citrate Plasma Versus Serum. Glucose 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 27156328-13 2016 CONCLUSIONS: Compared to the serum tube, NaF/citrate plasma tube is suitable for shipping venous whole blood samples within 10 hours at room temperature without undergoing significant glycolysis. Citric Acid 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 26402127-5 2016 Currently, little evidence has accrued to support the superiority of 18F-fluoride (18F-NaF) PET in diagnosing osseous metastases or monitoring treatment response in breast cancer when compared with conventional imaging. Fluoride ion f-18 69-81 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 27630735-8 2016 In vitro studies using TNF-alpha and IFN-gamma treated HaCaT cells revealed that VAL inhibited the exaggerated expression of Th2 chemokines including TARC/CCL17, MDC/CCL22, and proinflammatory chemokines such as CXCL8, GM-CSF, and I-CAM through blockade of the NF-kappaB pathway. valencene 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 212-217 26457748-13 2016 CONCLUSION: These data point to neutrophil Toll-like receptor 9 expression in acetaminophen-induced acute liver failure being mediated both by circulating endogenous DNA as well as ammonia and interleukin-8 in a synergistic manner inducing systemic inflammation, neutrophil exhaustion, and exacerbating hepatic encephalopathy. Acetaminophen 78-91 C-X-C motif chemokine ligand 8 Homo sapiens 193-206 27041244-3 2016 We studied the effect of rosuvastatin monotherapy or its combination at a lower dose with omega-3 polyunsaturated fatty acids (omega-3 PUFAs) in the VEGF and IL-8 plasma levels in patients with mixed dyslipidaemia. Rosuvastatin Calcium 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 27041244-3 2016 We studied the effect of rosuvastatin monotherapy or its combination at a lower dose with omega-3 polyunsaturated fatty acids (omega-3 PUFAs) in the VEGF and IL-8 plasma levels in patients with mixed dyslipidaemia. Fatty Acids, Omega-3 90-125 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 27041244-3 2016 We studied the effect of rosuvastatin monotherapy or its combination at a lower dose with omega-3 polyunsaturated fatty acids (omega-3 PUFAs) in the VEGF and IL-8 plasma levels in patients with mixed dyslipidaemia. Fatty Acids, Omega-3 127-140 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 27041244-11 2016 CONCLUSIONS: We show for the first time that either rosuvastatin monotherapy or its combination at a lower dose with omega-3 PUFAs reduces IL-8 levels in mixed dyslipidaemic patients. Rosuvastatin Calcium 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 27041244-11 2016 CONCLUSIONS: We show for the first time that either rosuvastatin monotherapy or its combination at a lower dose with omega-3 PUFAs reduces IL-8 levels in mixed dyslipidaemic patients. Fatty Acids, Omega-3 117-124 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 25045119-0 2016 Involvement of L-type Ca2+ channel and toll-like receptor-4 in nickel-induced interleukin-8 gene expression. Nickel 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 25045119-5 2016 The underlying mechanisms of nickel-induced IL-8 were investigated. Nickel 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 25045119-6 2016 We found that nickel induced IL-8 gene expression via the L-type Ca(2+) channel, Toll-like receptor-4 (TRL-4) and nuclear factor NF-kappaB signal transduction pathways. Nickel 14-20 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 25045119-7 2016 Nickel activated NF-kappaB expression through extracellular signal-regulated kinase 1/2 phosphorylation and then increased IL-8 expression. Nickel 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 25045158-8 2016 Exposure to pure canola oil (PCO) exhaust did not increase mediator production, but resulted in a significant decrease in IL-8 and RANTES in some cases. Rapeseed Oil 17-27 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 25045158-8 2016 Exposure to pure canola oil (PCO) exhaust did not increase mediator production, but resulted in a significant decrease in IL-8 and RANTES in some cases. PANTOTHENOYLAMINOETHENETHIOL 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 27820923-6 2016 The coexposure of 0.1 ppm NO2 and Der p 1, or 1 ppm NO2 and Der p 1 significantly increased both IL-6 and IL-8 release. Nitrogen Dioxide 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 26602157-5 2016 Furthermore, manumycin A was found to inhibit IL-1beta, IL-6, and IL-8 production in TNF alpha stimulated THP-1 cells and peripheral blood monocytes in a dose dependent manner (0.25-1 muM of manumycin A) without affecting cell viability. manumycin 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 26355467-11 2016 At week 14, IL-8 levels were significantly lower in the low vitamin D group compared with the normal vitamin D group (11.2 [9.1-13.8] versus 20.5 [17.9-37.2] pg/mL, P = 0.005). Vitamin D 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 27820923-6 2016 The coexposure of 0.1 ppm NO2 and Der p 1, or 1 ppm NO2 and Der p 1 significantly increased both IL-6 and IL-8 release. Nitrogen Dioxide 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 26530812-6 2016 LY-294002 blocked IL-8-induced p-AKT1 activation resulting in reduction of DNMT1 and increase of E-cadherin expression, whereas forced demethylation using 5-aza-2"-deoxycytidine restored E-cadherin expression. Decitabine 155-177 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 27579328-9 2016 Plasma IL-8 and IL-6 levels were significantly higher in patients with PaO2/FiO2 <= 200 mmHg and nonsurvivors than in those with PaO2/FiO2 > 200 mmHg and survivors. pao2 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 28078163-1 2016 A catalase-based (NAF/MWCNTs) nanocomposite film modified glassy carbon electrode for hydrogen peroxide (H2O2) detection was developed. Carbon 65-71 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 28078163-1 2016 A catalase-based (NAF/MWCNTs) nanocomposite film modified glassy carbon electrode for hydrogen peroxide (H2O2) detection was developed. Hydrogen Peroxide 86-103 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 28078163-1 2016 A catalase-based (NAF/MWCNTs) nanocomposite film modified glassy carbon electrode for hydrogen peroxide (H2O2) detection was developed. Hydrogen Peroxide 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 28116315-0 2016 LPS Cooperates with Poly-L-Arginine to Promote IL-6 and IL-8 Release via the JNK Signaling Pathway in NCI-H292 Cells. polyarginine 20-35 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 28116315-2 2016 Herein, we aimed to study the mechanism whereby poly-L-arginine (PLA) and lipopolysaccharide (LPS) can synergistically induce the release of interleukin-6 (IL-6) and IL-8 in NCI-H292 cells. polyarginine 48-63 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 28116315-2 2016 Herein, we aimed to study the mechanism whereby poly-L-arginine (PLA) and lipopolysaccharide (LPS) can synergistically induce the release of interleukin-6 (IL-6) and IL-8 in NCI-H292 cells. polyarginine 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 28116315-7 2016 The effects of SP600125, an inhibitor of the JNK pathway, on the increase of p-JNK, IL-6, and IL-8 were also studied. pyrazolanthrone 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 27294162-7 2016 The placental extravillous layer of the MGH showed high levels of IL-4, IL-6, IL-10, IL-17, and IFN-gamma and low levels of IL-1beta and IL-8, whereas the placental villous layer contained high levels of IL-17 and IFN-gamma. mgh 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 27579328-9 2016 Plasma IL-8 and IL-6 levels were significantly higher in patients with PaO2/FiO2 <= 200 mmHg and nonsurvivors than in those with PaO2/FiO2 > 200 mmHg and survivors. pao2 132-136 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 28116315-11 2016 Furthermore, SP600125 significantly inhibited the activation of JNK signal, as well as reducing the productions of IL-6 and IL-8 in response to PLA+LPS stimulation. pyrazolanthrone 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 27579328-9 2016 Plasma IL-8 and IL-6 levels were significantly higher in patients with PaO2/FiO2 <= 200 mmHg and nonsurvivors than in those with PaO2/FiO2 > 200 mmHg and survivors. fio2 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 26507542-6 2016 Quercetin also prevented INDO-induced ICAM-1 and P-selectin expressions and the increase of myeloperoxidase activity in gastric and ileal tissues and NF-kappaB activation and IL-8 production in Caco-2 cells. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 26431069-9 2016 Administration of 10 muM PD98059 significantly decreased IL-6 levels in the AF-MPhi coculture, and decreased the levels of TNF alpha and IL-8 in both the AF-MPhi and NP-MPhi cocultures. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 27713770-9 2016 Discussion:Altered levels of Vit D affect the balance between LL-37, IL-8 and SAA, suggesting an association with AAU, an extra-articular manifestation of AS. Vitamin D 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 26507542-6 2016 Quercetin also prevented INDO-induced ICAM-1 and P-selectin expressions and the increase of myeloperoxidase activity in gastric and ileal tissues and NF-kappaB activation and IL-8 production in Caco-2 cells. Indomethacin 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 26804595-14 2016 IL-8 antagonist and other anti-inflammation drugs like macrolides antibiotics, glucocorticoid and atorvastatin might be optional to resist the liquid cavity expanding as actually occurs obvious bleeding soon. Macrolides 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 25798666-3 2016 The exposure of human glomerulus renal endothelial cells to cadmium promotes a polarized apical secretion of IL-6 and IL-8, two pivotal proinflammatory cytokines known to play a significant role in renal inflammation. Cadmium 60-67 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 31529920-9 2016 The content of angiotensin II and endothelin I-21 correlates with level of interleukin-6 (r=0.416 and 0.445 correspondingly) and concentration of homocysteine with content of interleukin-8 (r=0.0459). Homocysteine 146-158 C-X-C motif chemokine ligand 8 Homo sapiens 175-188 27924706-7 2016 No significant association was found between airborne metal concentrations and biomarkers of inflammation in NALF, whereas increasing metal concentrations in NALF resulted in increased concentrations of total protein, IL-8, MMP-9, and TIMP-1. Metals 134-139 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 26804595-14 2016 IL-8 antagonist and other anti-inflammation drugs like macrolides antibiotics, glucocorticoid and atorvastatin might be optional to resist the liquid cavity expanding as actually occurs obvious bleeding soon. Atorvastatin 98-110 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 27651560-4 2016 Differentiation (BAP) and IL-8 production remained unchanged or decreased irrespective of the coating and surface; only the serum and plasma/platelets-coated ZrO2 exhibited higher BAP and IL-8 expression. zirconium oxide 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 27725392-5 2016 Under the gaseous phase administration, acetic acid and mixed acids caused a slight increase, decrease and increase on the interleukin-8 production, the mRNA expression of the heme oxygenase-1 (HO-1) gene and the HO-1 production, respectively, at one or more time points. Acetic Acid 40-51 C-X-C motif chemokine ligand 8 Homo sapiens 123-136 26140472-1 2016 OBJECTIVE: To compare the findings in rheumatoid arthritis (RA)-affected joints between (18)F-fluorodeoxyglucose (FDG) and (18)F-fluoride (NaF) positron emission tomography (PET)/computed tomography (CT). f-fluoride 127-137 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 26140472-7 2016 The SUVmax of (18)F-FDG correlated with that of (18)F-NaF in individual joints (r = 0.65), though detail distribution was different between two tracers. Fluorodeoxyglucose F18 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 26510735-10 2016 Stimulation with PAF + LPS resulted in higher IL-8 release (1959.3 +- 52.3) than control (141.2 +- 12.4), LPS (167.3 +- 65.8), or PAF (1527.2 +- 129.4) treatment (p < 0.05). Platelet Activating Factor 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 27994266-8 2016 In both RA and OA patient groups, stimulation of SAAT explants with IL-1beta (1 ng/ml/100 mg tissue) significantly up-regulated release of pro-(IL-6, IL-8, tumor necrosis factor - TNF) and anti-inflammatory (IL-10) cytokines but had no effect on the secretion of adiponectin, leptin, MIF and hepatocyte growth factor (HGF). saat 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 26740864-8 2016 Changes in IL-8, MIP-1beta, and MCP-1 serum concentrations may be associated with efficacy of pegIFNalpha- and ribavirin-based therapies in patients coinfected by HCV and HIV. pegifnalpha 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 26740864-8 2016 Changes in IL-8, MIP-1beta, and MCP-1 serum concentrations may be associated with efficacy of pegIFNalpha- and ribavirin-based therapies in patients coinfected by HCV and HIV. Ribavirin 111-120 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 28654417-4 2016 PROCEDURES: In this article, bone turnover and remodeling was studied using [18F]-sodium fluoride (NaF) PET data. Sodium Fluoride 82-97 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 27050899-0 2016 Nicorandil Inhibits Cyclic Strain-Induced Interleukin-8 Expression in Human Umbilical Vein Endothelial Cells. Nicorandil 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 27050899-2 2016 This study examined the effect of nicorandil on cyclic strain-induced interleukin-8 (IL-8) expression in human umbilical vein endothelial cells (HUVECs). Nicorandil 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 27050899-2 2016 This study examined the effect of nicorandil on cyclic strain-induced interleukin-8 (IL-8) expression in human umbilical vein endothelial cells (HUVECs). Nicorandil 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 27050899-6 2016 Nicorandil (1-10 mumol/l) inhibited cyclic strain-induced IL-8 expression, whereas 5-hydroxydecanoate (100 mumol/l), a selective inhibitor of the mitoKATP channel, completely reversed the inhibitory effects of nicorandil on cyclic strain-induced IL-8 expression. Nicorandil 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 27050899-6 2016 Nicorandil (1-10 mumol/l) inhibited cyclic strain-induced IL-8 expression, whereas 5-hydroxydecanoate (100 mumol/l), a selective inhibitor of the mitoKATP channel, completely reversed the inhibitory effects of nicorandil on cyclic strain-induced IL-8 expression. 5-hydroxydecanoic acid 83-101 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 27050899-8 2016 In addition, cobalt protoporphyrin (10 mumol/l), an inducer of HO-1 expression, mimicked the effects of nicorandil and inhibited IL-8 expression under cyclic strain, whereas zinc protoporphyrin IX (10 mumol/l), an inhibitor of HO-1 expression, antagonized the effect of nicorandil. cobaltiprotoporphyrin 13-34 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 27050899-9 2016 HO-1 silencing significantly abrogated the inhibitory effects of nicorandil on cyclic strain-induced IL-8 expression, suggesting that HO-1 plays a role in the mechanism of action of nicorandil. Nicorandil 65-75 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 27050899-9 2016 HO-1 silencing significantly abrogated the inhibitory effects of nicorandil on cyclic strain-induced IL-8 expression, suggesting that HO-1 plays a role in the mechanism of action of nicorandil. Nicorandil 182-192 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 27050899-10 2016 KEY MESSAGES: This study is the first to report that nicorandil inhibits cyclic strain-induced IL-8 expression through the induction of HO-1 expression in HUVECs. Nicorandil 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 26477783-6 2016 RESULTS: LPS, fMLP, imiquimod and R848 stimulated the release of CXCL8, NE and MMP-9 whereas poly I:C selectively induced CXCL8 release only. Poly I-C 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 26202066-6 2016 In addition, the NOD2 pathway up-regulation was functional, as stimulation of PBMCs with muramyl dipeptide (MDP) induced the production of higher amounts of tumour necrosis factor (TNF)-alpha, interleukin (IL)-8, and IL-1beta compared with OA PBMCs. Acetylmuramyl-Alanyl-Isoglutamine 89-106 C-X-C motif chemokine ligand 8 Homo sapiens 193-211 27014812-6 2016 CONCLUSION: Formaldehyde exposure can cause imbalance between Th1 and Th2 cytokines secreted by 16HBE cells, as well as increased expression of IL-8 and TNF-alpha. Formaldehyde 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 26782552-0 2015 Sevoflurane downregulates interleukin-6 and interleukin-8 levels in patients after cardiopulmonary bypass surgery: a meta-analysis. Sevoflurane 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 26782552-1 2015 This study aimed to investigate the effect of sevoflurane on serum levels of interleukin (IL)-6 and IL-8 in patients who underwent cardiopulmonary bypass (CPB). Sevoflurane 46-57 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 26782552-2 2015 The strength of the association between sevoflurane treatment and serum level of IL-6 and IL-8 was determined in patients who underwent CPB by summary standard mean differences (SMDs); 95% confidence interval (CI) was used. Sevoflurane 40-51 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 26782552-3 2015 In total, seven case-control studies showed decreased IL-6 and IL-8 levels in sevoflurane-treated patients than in controls (IL-6: SMD = 1.56, 95%CI: 0.95-2.17, P < 0.001; IL-8: SMD = 1.63, 95%CI: 0.30-2.96, P < 0.001, respectively). Sevoflurane 78-89 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 26782552-3 2015 In total, seven case-control studies showed decreased IL-6 and IL-8 levels in sevoflurane-treated patients than in controls (IL-6: SMD = 1.56, 95%CI: 0.95-2.17, P < 0.001; IL-8: SMD = 1.63, 95%CI: 0.30-2.96, P < 0.001, respectively). Sevoflurane 78-89 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 26782552-4 2015 Further, IL-6 and IL-8 levels were significantly higher in sevoflurane-treated patients than in sevoflurane-pretreated patients (IL-6 post vs pre: SMD = 2.17, 95%CI: 1.40-2.95, P < 0.001; IL-8 post vs pre: SMD = 4.01, 95%CI: 2.80-5.21, P < 0.001, respectively). Sevoflurane 59-70 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 26782552-4 2015 Further, IL-6 and IL-8 levels were significantly higher in sevoflurane-treated patients than in sevoflurane-pretreated patients (IL-6 post vs pre: SMD = 2.17, 95%CI: 1.40-2.95, P < 0.001; IL-8 post vs pre: SMD = 4.01, 95%CI: 2.80-5.21, P < 0.001, respectively). Sevoflurane 59-70 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 26782552-4 2015 Further, IL-6 and IL-8 levels were significantly higher in sevoflurane-treated patients than in sevoflurane-pretreated patients (IL-6 post vs pre: SMD = 2.17, 95%CI: 1.40-2.95, P < 0.001; IL-8 post vs pre: SMD = 4.01, 95%CI: 2.80-5.21, P < 0.001, respectively). Sevoflurane 96-107 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 26782552-5 2015 CPB-stratified analysis showed significant decrease in IL-6 and IL-8 levels in sevoflurane-treated patients than in controls, irrespective of the time after CPB surgery (P < 0.05). Sevoflurane 79-90 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 26782552-6 2015 Moreover, sevoflurane-pretreated patients under the <12-h subgroup showed decreased IL-6 levels (P = 0.698), while all other subgroups showed decreased IL-8 levels (P < 0.05). Sevoflurane 10-21 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 26782552-7 2015 Further, subgroup analysis by different dose of sevoflurane showed decreased IL-6 and IL-8 levels in subgroups administered with a dose of <2 and >= 2% sevoflurane under the case vs control and pre- vs post-treatment of sevoflurane models. Sevoflurane 48-59 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 26782552-7 2015 Further, subgroup analysis by different dose of sevoflurane showed decreased IL-6 and IL-8 levels in subgroups administered with a dose of <2 and >= 2% sevoflurane under the case vs control and pre- vs post-treatment of sevoflurane models. Sevoflurane 158-169 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 26782552-7 2015 Further, subgroup analysis by different dose of sevoflurane showed decreased IL-6 and IL-8 levels in subgroups administered with a dose of <2 and >= 2% sevoflurane under the case vs control and pre- vs post-treatment of sevoflurane models. Sevoflurane 158-169 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 26782552-8 2015 Serum IL-6 and IL-8 levels were significantly lower in sevoflurane-treated patients who underwent CPB, suggesting sevoflurane pretreatment to be more beneficial than post-treatment. Sevoflurane 55-66 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 26782552-8 2015 Serum IL-6 and IL-8 levels were significantly lower in sevoflurane-treated patients who underwent CPB, suggesting sevoflurane pretreatment to be more beneficial than post-treatment. Sevoflurane 114-125 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 26689258-7 2015 However, when the peptides were mutated on two lysine residues (K15 and K20), the inhibition effects were greatly reduced indicating these two amino acids are key residues for the initial binding of CXCL8 to CXCR1. Lysine 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 199-204 26491069-9 2015 Finally, activation of ATM and DNA damage signaling suppress cytokine production and can abrogate the overproduction of IL-8 in ROS-deficient cells. Reactive Oxygen Species 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 26629712-4 2015 Nucleus-independent chemical shift was employed to monitor the ionic processes of NaF aqueous electrolyte in nanopores of carbon supercapacitors. Carbon 122-128 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 26672987-5 2015 RESULTS: Healthy individuals supplemented with omega-3 FA had differential responses in prostaglandin-endoperoxide synthase 1 (PTGS1), prostaglandin-endoperoxide synthase 2 (PTGS2), arachidonate 12-lipoxygenase (ALOX12), and interleukin 8 (IL-8) gene expression in isolated PBMCs. Fatty Acids, Omega-3 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 225-238 26674118-3 2015 Here we identify IL-8 as a hypoxia-regulated cytokine in both AML cell lines and primary AML samples that is induced within 48 hours of severe hypoxia (1% O2). Oxygen 155-157 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 26633568-2 2015 We find a large surface band gap (E(g)(Surf), up to 2.52 eV) for a NaF/KF-postdeposition treated (PDT) absorber significantly increases compared to the CIGSe bulk band gap and to the Eg(Surf) of 1.61 eV found for an absorber treated with NaF only. surf 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 26633568-2 2015 We find a large surface band gap (E(g)(Surf), up to 2.52 eV) for a NaF/KF-postdeposition treated (PDT) absorber significantly increases compared to the CIGSe bulk band gap and to the Eg(Surf) of 1.61 eV found for an absorber treated with NaF only. surf 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 238-241 26633568-2 2015 We find a large surface band gap (E(g)(Surf), up to 2.52 eV) for a NaF/KF-postdeposition treated (PDT) absorber significantly increases compared to the CIGSe bulk band gap and to the Eg(Surf) of 1.61 eV found for an absorber treated with NaF only. lysylphenylalanine 71-73 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 26633568-2 2015 We find a large surface band gap (E(g)(Surf), up to 2.52 eV) for a NaF/KF-postdeposition treated (PDT) absorber significantly increases compared to the CIGSe bulk band gap and to the Eg(Surf) of 1.61 eV found for an absorber treated with NaF only. lysylphenylalanine 71-73 C-X-C motif chemokine ligand 8 Homo sapiens 238-241 26633568-2 2015 We find a large surface band gap (E(g)(Surf), up to 2.52 eV) for a NaF/KF-postdeposition treated (PDT) absorber significantly increases compared to the CIGSe bulk band gap and to the Eg(Surf) of 1.61 eV found for an absorber treated with NaF only. surf 186-190 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 26672987-5 2015 RESULTS: Healthy individuals supplemented with omega-3 FA had differential responses in prostaglandin-endoperoxide synthase 1 (PTGS1), prostaglandin-endoperoxide synthase 2 (PTGS2), arachidonate 12-lipoxygenase (ALOX12), and interleukin 8 (IL-8) gene expression in isolated PBMCs. Fatty Acids, Omega-3 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 240-244 26515417-7 2015 In contrast to clopidogrel, ticagrelor also significantly reduced peak levels of IL-8 and growth colony-stimulating factor and increased peak levels of the anti-inflammatory cytokine IL-10. Ticagrelor 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 26677330-9 2015 Baseline serum levels of interleukin-6 (Z=-2.155; P=0.031) and interleukin-8 (Z=-2.616; P=0.009) were significantly higher when moderate-to-severe AEs were present (n=13 patients with moderate-to-severe AEs). aes 147-150 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 26641100-7 2015 ANCE-induced IL-6, IL-8, and MCP-1 release was inhibited by IL-1 receptor antagonist and by an IKK2 inhibitor (a blocker of NF-kappaB signaling) in a concentration-dependent manner, but was not affected by a pan-caspase inhibitor (Z-VAD-FMK). ance 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 26420839-9 2015 Patient hTEC produced and secreted elevated amounts of the pro-inflammatory cytokine IL8, which was highly correlated with the acridine orange staining. Acridine Orange 127-142 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 26420839-10 2015 Summarizing, hTEC of MMAuria patients are characterized by disturbed energy metabolism and ROS production that lead to increased autophagy and IL8 secretion. Reactive Oxygen Species 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 143-146 26677330-11 2015 CONCLUSION: These results demonstrate that serum levels of interleukin-6, interleukin-8, and macrophage inflammatory protein-1beta as potential blood biomarkers could be utilized to identify the responsiveness of patients to serotonin and norepinephrine reuptake inhibitor like milnacipran, or to identify those patients who may experience AEs strong enough to warrant discontinuation of treatment. Serotonin 225-234 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 26266556-13 2015 SCFAs induced a dose-dependent and pertussis toxin-sensitive IL-8 response in bronchial epithelial cells, with a higher production of IL-8 in CFBE41o(-) than in 16HBE14o(-) cells. Fatty Acids, Volatile 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 26266556-13 2015 SCFAs induced a dose-dependent and pertussis toxin-sensitive IL-8 response in bronchial epithelial cells, with a higher production of IL-8 in CFBE41o(-) than in 16HBE14o(-) cells. Fatty Acids, Volatile 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 25969431-9 2015 In human OA synovium, paquinimod blocked proinflammatory (interleukin (IL)-6, IL-8, tumour necrosis factor-alpha) and catabolic (matrix metalloproteinases 1 and 3) factors induced by S100A9 (n=5). paquinimod 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 26163999-8 2015 In conclusion, pretreatment serum IL-8 is a useful prognostic marker for TACE refractoriness and LT-free survival in TACE-treated patients with HBV-associated HCC. Chlorotrianisene 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 26373407-4 2015 The chloride ions can, in a third step, be exchanged with fluoride ions by immersion of the ionomer in NaF solution. Chlorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 26373407-4 2015 The chloride ions can, in a third step, be exchanged with fluoride ions by immersion of the ionomer in NaF solution. Fluorides 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 26396142-6 2015 Mechanistic studies have shown that calcitriol-active form of vitamin D-influences inflammatory processes involved in cancer progression, including the enzyme cyclooxygenase 2, the NF-kappaB pathway, and the expression of the cytokines TNFalpha, IL1beta, IL6, IL8, IL17, and TGFbeta1. Calcitriol 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 260-263 26396142-6 2015 Mechanistic studies have shown that calcitriol-active form of vitamin D-influences inflammatory processes involved in cancer progression, including the enzyme cyclooxygenase 2, the NF-kappaB pathway, and the expression of the cytokines TNFalpha, IL1beta, IL6, IL8, IL17, and TGFbeta1. Vitamin D 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 260-263 26387812-0 2015 Association of single nucleotide polymorphisms in IL8 and IL13 with sunitinib-induced toxicity in patients with metastatic renal cell carcinoma. Sunitinib 68-77 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 26303011-0 2015 PA401, a novel CXCL8-based biologic therapeutic with increased glycosaminoglycan binding, reduces bronchoalveolar lavage neutrophils and systemic inflammatory markers in a murine model of LPS-induced lung inflammation. pa401 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 26303011-0 2015 PA401, a novel CXCL8-based biologic therapeutic with increased glycosaminoglycan binding, reduces bronchoalveolar lavage neutrophils and systemic inflammatory markers in a murine model of LPS-induced lung inflammation. Glycosaminoglycans 63-80 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 26303011-3 2015 CXCL8 exerts its chemotactic activity by binding to its GPCR receptors (CXCR1/R2) located on neutrophils, as well as through interactions with glycosaminoglycans (GAGs) on cell surfaces including those of the microvascular endothelium. Glycosaminoglycans 143-161 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 26303011-3 2015 CXCL8 exerts its chemotactic activity by binding to its GPCR receptors (CXCR1/R2) located on neutrophils, as well as through interactions with glycosaminoglycans (GAGs) on cell surfaces including those of the microvascular endothelium. Glycosaminoglycans 163-167 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 26303011-5 2015 METHODS: We have engineered increased GAG-binding affinity into human CXCL8, thereby obtaining a competitive inhibitor that displaces wild-type IL-8/CXCL8 from GAGs. Glycosaminoglycans 160-164 C-X-C motif chemokine ligand 8 Homo sapiens 70-75 26303011-5 2015 METHODS: We have engineered increased GAG-binding affinity into human CXCL8, thereby obtaining a competitive inhibitor that displaces wild-type IL-8/CXCL8 from GAGs. Glycosaminoglycans 160-164 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 26303011-5 2015 METHODS: We have engineered increased GAG-binding affinity into human CXCL8, thereby obtaining a competitive inhibitor that displaces wild-type IL-8/CXCL8 from GAGs. Glycosaminoglycans 160-164 C-X-C motif chemokine ligand 8 Homo sapiens 149-154 26387812-4 2015 METHODS: In this exploratory study, we selected SNPs in genes CYP3A4, NR1I2, POR, IL8, IL13, IL4-R, HIF1A and MET that might possibly be associated with sunitinib treatment outcome. Sunitinib 153-162 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 26387812-10 2015 CONCLUSIONS: We show that polymorphisms in IL8 rs1126647 and IL13 rs1800925 are associated with sunitinib-induced toxicities. Sunitinib 96-105 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 26964198-5 2015 The samples upconversion luminescent spectra showed the intensity enhancement of red and green light emission peaks with increasement of the ratio of NaF/RE3+. re3+ 154-158 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 26964198-7 2015 The chromaticity coordinate diagram exhibited that the change of the luminescent color of samples could be achieved by adjusting the ratio of NaF/RE3+. re3+ 146-150 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 26964198-8 2015 With the increasing of NaF/RE3+ ratio, for the whole light-emitting colors of samples, the shift from yellow region to near red region could be realized. re3+ 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 26507163-6 2015 mRNA and protein expressions of IL-1beta and IL-8 decreased significantly when pretreated HCECs with recombinant human SP-D for 4h before A. fumigatus stimulation, while IL-1beta and IL-8 increased when pretreated with SP-D antibody for 1h. Hydrogen 237-239 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 26453510-5 2015 Levels of thymic stromal lymphopoietin, tumor necrosis factor (TNF)-alpha, IL-1beta, and IL-8 increased by IL-32 or LPS were significantly reduced by treatment with acteoside in THP-1 cells. acteoside 165-174 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 26453510-7 2015 In IL-32-induced macrophages, acteoside significantly reduced LPS-induced TNF-alpha, IL-1beta, IL-6, and IL-8 production. acteoside 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 26590116-6 2015 Artesunate reduced methacholine-induced airway hyper-responsiveness, suppressed pulmonary inflammation cell recruitment and IL-4, IL-8, IL-13 and TNF-alpha levels, selectively inhibited PI3Kdelta/Akt pathway, and restored HDAC2 activity. Artesunate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 26590116-8 2015 Glucocorticoid sensitivity was evaluated by the inhibition of TNF-alpha-induced IL-8 production by dexamethasone. Dexamethasone 99-112 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 26613389-13 2015 Combinations of BMI >= 30 with elevated IL-6, IL-8, hsCRP, TNF-alpha, and leptin predicted improved response to L-methylfolate calcium in MDD patients with an inadequate antidepressant response. levomefolate calcium 115-137 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 25715004-5 2015 RESULTS: Latanoprost stimulated the release of IL-6, IL-8, and MCP-1 from HTFs in a concentration-dependent and time-dependent manner, whereas timolol maleate and pilocarpine had no such effects. Latanoprost 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 26156812-5 2015 Calcitriol inhibited interleukin (IL)-6, IL-8, CC chemokine ligand (CCL) 20, CXC chemokine ligand (CXCL) 10, and matrix metalloproteinase (MMP)-3 release from IL-1beta-stimulated HPDLC. Calcitriol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 26156812-7 2015 Moreover, we found c-jun N-terminal kinase (JNK) phosphorylation and IkappaB-alpha degradation in IL-1beta-stimulated HPDLC were inhibited by calcitriol, and JNK and nuclear factor (NF)-kappaB inhibitors could decrease IL-6, IL-8, CCL20, CXCL10, and MMP-3 productions in IL-1beta-treated HPDLC. Calcitriol 142-152 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 26507164-8 2015 We found that icariin inhibited TNF-alpha/IFN-gamma-induced IL-6, IL-8, IL-1beta, and MCP-1 production in a dose-dependent manner; meanwhile, the icariin treatment inhibited the gene expression of IL-8, IL-1beta, ICAM-1 and TACR1 in HaCaT cells in a time- and dose-dependent manner. icariin 146-153 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 26507164-8 2015 We found that icariin inhibited TNF-alpha/IFN-gamma-induced IL-6, IL-8, IL-1beta, and MCP-1 production in a dose-dependent manner; meanwhile, the icariin treatment inhibited the gene expression of IL-8, IL-1beta, ICAM-1 and TACR1 in HaCaT cells in a time- and dose-dependent manner. icariin 146-153 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 26454222-14 2015 In contrast, NaF reduced step height when applied after citric acid immersion, but only in the presence of saliva. Citric Acid 56-67 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 25715004-7 2015 The latanoprost-induced release of IL-6, IL-8, and MCP-1 was attenuated by inhibitors of MAPK (PD98059, SB203580, or JNK inhibitor II) or NF-kappaB (IkappaB kinase 2 inhibitor) signaling pathways. Latanoprost 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 26297794-8 2015 Furthermore, the selective CXC chemokine receptor 2 and formyl peptide receptor 2 antagonists, SB225002 and WRW4, respectively, blocked the synergy between IL-8/CXC chemokine ligand 8 and serum amyloid A1alpha in neutrophil chemotaxis in vitro, indicating that for synergy their corresponding G protein-coupled receptors are required. SB 225002 95-103 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 26507164-8 2015 We found that icariin inhibited TNF-alpha/IFN-gamma-induced IL-6, IL-8, IL-1beta, and MCP-1 production in a dose-dependent manner; meanwhile, the icariin treatment inhibited the gene expression of IL-8, IL-1beta, ICAM-1 and TACR1 in HaCaT cells in a time- and dose-dependent manner. icariin 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 26507164-8 2015 We found that icariin inhibited TNF-alpha/IFN-gamma-induced IL-6, IL-8, IL-1beta, and MCP-1 production in a dose-dependent manner; meanwhile, the icariin treatment inhibited the gene expression of IL-8, IL-1beta, ICAM-1 and TACR1 in HaCaT cells in a time- and dose-dependent manner. icariin 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 26407807-7 2015 Activation of AMPK, using two pharmacologically distinct compounds, AICAR or phenformin, significantly suppressed LPS- or IL-1beta-induced gene expression and secretion of pro-inflammatory cytokine IL-6, the chemokines IL-8 and MCP-1, and COX-2 and subsequent prostaglandin release from adipose tissue and skeletal muscle. Phenformin 77-87 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 25712856-6 2015 RESULTS: In HGFs, histamine induced expression of CCL20 and IL8 genes in a time-dependent manner (p < 0.05). Histamine 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 25712856-7 2015 Combined stimulation with histamine and Pam3CSK4 or LPS led to a significant amplification in expression of CCL20 and IL-8 when compared with treatment with each stimulant alone (p < 0.05), and this effect was mediated via pathways involving the H1R (p < 0.05). Histamine 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 26350254-7 2015 These results were supported by experiments in the human colonic epithelial cell line Caco-2, where ALA supplementation was shown to be effective in inhibiting inflammation induced by IL-1beta by down-regulating mRNA levels of pro-inflammatory genes including IL-8, COX2 and inducible nitric oxide synthase. alpha-Linolenic Acid 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 260-264 26334245-9 2015 Pharmacologic and siRNA-mediated inhibition of PLD1 and PLD2 attenuated the nicotine- and LPS-induced upregulation of inducible nitric oxide (NO) synthase and cyclooxygenase-2, production of NO, and prostaglandin E2, and mRNA expression and secretion of tumor necrosis factor-alpha, interleukin (IL)-1beta, and IL-8. Nicotine 76-84 C-X-C motif chemokine ligand 8 Homo sapiens 311-315 26378490-1 2015 BACKGROUND: PET/computed tomography (CT) imaging with the sodium-(F)-fluoride/2-(F)-fluoro-2-deoxy-D-glucose (F-NaF/F-FDG) cocktail has been proposed for patients with osseous metastases. 2-(f)-fluoro-2-deoxy-d-glucose 78-108 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 26378490-12 2015 When the F-NaF : F-FDG ratio changed from 1 : 8 to 1 : 2, the typical SUV on the generated PET images increased by 50%, whereas the change in the uptake visual pattern was hardly noticeable. f-fdg 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 26378490-13 2015 CONCLUSION: F-NaF and F-FDG in the cocktail contribute equally to image formation when the F-NaF : F-FDG ratio is 1 : 5. f-fdg 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 26319029-4 2015 On the contrary, increased upregulation of CD86 and interleukin 8 (IL-8) production were observed in THP-1 cells exposed to combinations of citral (Cit) or imidazolidinyl urea (IMZ) with DBP, indicative of an adjuvant effect. citral 140-146 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 26549126-10 2015 Treatments with IL-8, LPS, ET-1 and dexamethasone were able to increase three to fourfold Ucn1 release from cultured endothelial cells. Dexamethasone 36-49 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 26270575-6 2015 RESULTS: DHA significantly attenuated IL-1beta induced proinflammatory IL-8 and IL-6 protein and mRNA in fetal H4, NEC-IEC, and mature Caco2, NCM460 IEC, compared to control and PAL treatment. Docosahexaenoic Acids 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 26270575-8 2015 ARA had potent anti-inflammatory effects with lower IL-8 and IL-6 (protein and mRNA) in fetal H4 but not in NEC-IEC or adult IEC. Arachidonic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 26319029-4 2015 On the contrary, increased upregulation of CD86 and interleukin 8 (IL-8) production were observed in THP-1 cells exposed to combinations of citral (Cit) or imidazolidinyl urea (IMZ) with DBP, indicative of an adjuvant effect. citral 140-146 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26319029-4 2015 On the contrary, increased upregulation of CD86 and interleukin 8 (IL-8) production were observed in THP-1 cells exposed to combinations of citral (Cit) or imidazolidinyl urea (IMZ) with DBP, indicative of an adjuvant effect. citral 148-151 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 26319029-4 2015 On the contrary, increased upregulation of CD86 and interleukin 8 (IL-8) production were observed in THP-1 cells exposed to combinations of citral (Cit) or imidazolidinyl urea (IMZ) with DBP, indicative of an adjuvant effect. citral 148-151 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26319029-4 2015 On the contrary, increased upregulation of CD86 and interleukin 8 (IL-8) production were observed in THP-1 cells exposed to combinations of citral (Cit) or imidazolidinyl urea (IMZ) with DBP, indicative of an adjuvant effect. imidazolidinyl urea 156-175 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 26319029-4 2015 On the contrary, increased upregulation of CD86 and interleukin 8 (IL-8) production were observed in THP-1 cells exposed to combinations of citral (Cit) or imidazolidinyl urea (IMZ) with DBP, indicative of an adjuvant effect. imidazolidinyl urea 156-175 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26319029-4 2015 On the contrary, increased upregulation of CD86 and interleukin 8 (IL-8) production were observed in THP-1 cells exposed to combinations of citral (Cit) or imidazolidinyl urea (IMZ) with DBP, indicative of an adjuvant effect. imidazolidinyl urea 177-180 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 26319029-4 2015 On the contrary, increased upregulation of CD86 and interleukin 8 (IL-8) production were observed in THP-1 cells exposed to combinations of citral (Cit) or imidazolidinyl urea (IMZ) with DBP, indicative of an adjuvant effect. imidazolidinyl urea 177-180 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26463037-5 2015 Thrombin-induced IL-8/CXCL8 release was inhibited by CK2 inhibitors (apigenin and tetrabromobenzotriazole, TBB), small interfering RNA of CK2beta (CK2beta siRNA), and MSK1 siRNA. tetrabromobenzotriazole 82-105 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 26739470-10 2015 CONCLUSION: Stimulation of hepatocytes by the PA fatty acid in vitro promotes mRNA expression of TNF-alpha, MCP-1 and IL-8, but overexpression of JAZF1 inhibits the PA-induced expression and secretion of these factors. pa fatty acid 46-59 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 26739470-10 2015 CONCLUSION: Stimulation of hepatocytes by the PA fatty acid in vitro promotes mRNA expression of TNF-alpha, MCP-1 and IL-8, but overexpression of JAZF1 inhibits the PA-induced expression and secretion of these factors. Palmitic Acid 46-48 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 26551350-5 2015 l-Trp treatment (5 mM) reduced TNF-alpha-induced IL-8 secretion from HT-29 or Caco-2 cells to about 50 or 40%, respectively. Tryptophan 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 25970774-8 2015 Gemcitabine-treatment of PC cells induced expression of various growth factors/cytokines, including IL-8, which exhibited greatest upregulation. gemcitabine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 26410779-5 2015 The analysis of pro-inflammatory cytokines release by ELISA revealed that resveratrol, lipoic acid melatonin and Co-Q10 inhibited the BBB endothelial release of pro-inflammatory cytokines IL-6 and IL-8, reduced (not Co-Q10) CSE-induced up-regulation of Platelet Cell Adhesion Molecule-1 (PECAM-1), Vascular Cell Adhesion Molecule-1 (VCAM-1) & E-selectin and inhibited monocytes-endothelial cell adhesion. Resveratrol 74-85 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 26410779-5 2015 The analysis of pro-inflammatory cytokines release by ELISA revealed that resveratrol, lipoic acid melatonin and Co-Q10 inhibited the BBB endothelial release of pro-inflammatory cytokines IL-6 and IL-8, reduced (not Co-Q10) CSE-induced up-regulation of Platelet Cell Adhesion Molecule-1 (PECAM-1), Vascular Cell Adhesion Molecule-1 (VCAM-1) & E-selectin and inhibited monocytes-endothelial cell adhesion. lipoic acid melatonin 87-108 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 26410779-5 2015 The analysis of pro-inflammatory cytokines release by ELISA revealed that resveratrol, lipoic acid melatonin and Co-Q10 inhibited the BBB endothelial release of pro-inflammatory cytokines IL-6 and IL-8, reduced (not Co-Q10) CSE-induced up-regulation of Platelet Cell Adhesion Molecule-1 (PECAM-1), Vascular Cell Adhesion Molecule-1 (VCAM-1) & E-selectin and inhibited monocytes-endothelial cell adhesion. coenzyme Q10 113-119 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 26572585-4 2015 EC overexpression of mutant ITGB4 with specific tyrosines mutated to phenylalanine (Y1440, Y1526 Y1640, or Y1422) resulted in significantly attenuated CS-induced cytokine expression (IL6, IL-8, MCP-1, and RANTES). Cesium 151-153 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 26463037-5 2015 Thrombin-induced IL-8/CXCL8 release was inhibited by CK2 inhibitors (apigenin and tetrabromobenzotriazole, TBB), small interfering RNA of CK2beta (CK2beta siRNA), and MSK1 siRNA. tetrabromobenzotriazole 82-105 C-X-C motif chemokine ligand 8 Homo sapiens 22-27 26885050-6 2015 In this study, we showed Dex inhibited the increase in cTnI and CK-MB, attenuated the production of pro-inflammatory cytokines TNF-alpha, IL-6 and IL-8, and promoted anti-inflammatory cytokine IL-10 production. Dexmedetomidine 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 26885173-9 2015 RESULTS: Compared with those in normal glucose condition, IL-6 and IL-8 expression were increased in high glucose condition. Glucose 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26463037-5 2015 Thrombin-induced IL-8/CXCL8 release was inhibited by CK2 inhibitors (apigenin and tetrabromobenzotriazole, TBB), small interfering RNA of CK2beta (CK2beta siRNA), and MSK1 siRNA. 2-ethylhexyl 2,3,4,5-tetrabromobenzoate 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 26885173-9 2015 RESULTS: Compared with those in normal glucose condition, IL-6 and IL-8 expression were increased in high glucose condition. Glucose 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26463037-5 2015 Thrombin-induced IL-8/CXCL8 release was inhibited by CK2 inhibitors (apigenin and tetrabromobenzotriazole, TBB), small interfering RNA of CK2beta (CK2beta siRNA), and MSK1 siRNA. 2-ethylhexyl 2,3,4,5-tetrabromobenzoate 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 22-27 29124230-14 2015 In addition, SB203580 (p38 inhibitor) and U0126 (ERK1/2 inhibitor) significantly suppressed the expression of TNF-alpha and IL-8 in LPS-stimulated THP-1 cells. SB 203580 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 26573531-5 2015 Immediately after treatment with poly(I:C), PHF11, IL8, and interferon-dependent ISG15 RNA expression was increased. poly 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 26553339-5 2015 In hypoxia and serum-deprived culture conditions, LPA induces CD34(+) cell proliferation without maintaining the their undifferentiating state, and enhances IL-8, IL-6 and G-CSF secretion during the first 12 h compared to non-treated cells. lysophosphatidic acid 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 29124230-14 2015 In addition, SB203580 (p38 inhibitor) and U0126 (ERK1/2 inhibitor) significantly suppressed the expression of TNF-alpha and IL-8 in LPS-stimulated THP-1 cells. U 0126 42-47 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 26614998-10 2015 The propofol could inhibit the expression of IL-6, IL-8 and TNF-alpha caused by LPS. Propofol 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 26531309-9 2015 However, PSA-TMC-ODN and PSA-TMC-ODN-MTX resulted in significant decreases in the inflammatory mediators IL-6 and IL-8 in both cell models. tmc-odn 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 26531309-9 2015 However, PSA-TMC-ODN and PSA-TMC-ODN-MTX resulted in significant decreases in the inflammatory mediators IL-6 and IL-8 in both cell models. psa-tmc-odn-mtx 25-40 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 26296578-8 2015 Resveratrol exerted a high, dose-dependent, antiviral activity against HRV-16 replication and reduced virus-induced secretion of IL-6, IL-8 and RANTES to levels similar to that of uninfected nasal epithelia. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 25847254-3 2015 We found that 10-MDP caused the release of inflammatory cytokines including NO, PGE2, iNOS, COX-2, TNF-alpha, IL-1beta, IL-6 and IL-8 in a concentration-dependent manner. methacryloyloxydecyl dihydrogen phosphate 14-20 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 26614998-11 2015 After the intervention treatment of 50 mug/mL propofol, the concentration of IL-6, IL-8 and TNF-alpha was significantly decreased (P < 0.01). Propofol 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 26535082-6 2015 PKC inhibitors, MAPK inhibitors, and ROS quenchers also significantly attenuated expression of CXCL8. ros 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 26354876-8 2015 This compound behaves like the prototypic AhR ligand 6-formylindolo[3,2-b]carbazole, a cutaneous UV light-induced tryptophan metabolite, both promoting IL-22, IL-8, and CCL2 secretion by T-cells and macrophages. 6-formylindolo(3,2-b)carbazole 53-83 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 25969155-6 2015 The highest %SHR and the lowest DeltaKHN were seen for the 5% NaF/5% TMP varnish, followed by 5% NaF and placebo. trimetaphosphoric acid 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 25969155-7 2015 CONCLUSION: The remineralizing effect of a 5% NaF varnish is significantly enhanced when associated with TMP. trimetaphosphoric acid 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 26133785-2 2015 The dysfunctional effect of CFTR mutations, principally the F508del-CFTR mutant, is further manifested by hypersecretion of the pro-inflammatory chemokine interleukin-8 into the airway lumen, which further contributes to morbidity and mortality. f508del 60-67 C-X-C motif chemokine ligand 8 Homo sapiens 155-168 26386353-9 2015 Similarly, pretreatment with FeSO4 stimulated H2O2-induced TRPM2 activation at 37 C in U937 cells and enhanced H2O2-induced ERK phosphorylation and interleukin-8 (CXCL8) production. ferrous sulfate 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 26386353-9 2015 Similarly, pretreatment with FeSO4 stimulated H2O2-induced TRPM2 activation at 37 C in U937 cells and enhanced H2O2-induced ERK phosphorylation and interleukin-8 (CXCL8) production. ferrous sulfate 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 163-168 26386353-0 2015 Sensitization of H2O2-induced TRPM2 activation and subsequent interleukin-8 (CXCL8) production by intracellular Fe(2+) in human monocytic U937 cells. Hydrogen Peroxide 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 26386353-0 2015 Sensitization of H2O2-induced TRPM2 activation and subsequent interleukin-8 (CXCL8) production by intracellular Fe(2+) in human monocytic U937 cells. Hydrogen Peroxide 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 77-82 26386353-0 2015 Sensitization of H2O2-induced TRPM2 activation and subsequent interleukin-8 (CXCL8) production by intracellular Fe(2+) in human monocytic U937 cells. ammonium ferrous sulfate 112-118 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 26386353-0 2015 Sensitization of H2O2-induced TRPM2 activation and subsequent interleukin-8 (CXCL8) production by intracellular Fe(2+) in human monocytic U937 cells. ammonium ferrous sulfate 112-118 C-X-C motif chemokine ligand 8 Homo sapiens 77-82 26386353-9 2015 Similarly, pretreatment with FeSO4 stimulated H2O2-induced TRPM2 activation at 37 C in U937 cells and enhanced H2O2-induced ERK phosphorylation and interleukin-8 (CXCL8) production. Hydrogen Peroxide 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 163-168 26386353-9 2015 Similarly, pretreatment with FeSO4 stimulated H2O2-induced TRPM2 activation at 37 C in U937 cells and enhanced H2O2-induced ERK phosphorylation and interleukin-8 (CXCL8) production. Hydrogen Peroxide 111-115 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 26386353-9 2015 Similarly, pretreatment with FeSO4 stimulated H2O2-induced TRPM2 activation at 37 C in U937 cells and enhanced H2O2-induced ERK phosphorylation and interleukin-8 (CXCL8) production. Hydrogen Peroxide 111-115 C-X-C motif chemokine ligand 8 Homo sapiens 163-168 26386353-10 2015 Although the addition of H2O2 to cells under conditions of intracellular Fe(2+)-accumulation caused cell death, concentration of H2O2 required for CXCL8 production was lower than that resulting in cell death. Hydrogen Peroxide 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 147-152 26386353-11 2015 These results indicate that intracellular Fe(2+)-accumulation sensitizes TRPM2 channels to H2O2 and subsequently produces CXCL8 at around body temperature. ammonium ferrous sulfate 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 25919965-5 2015 VEGF regulated other important angiogenic proteins including PAI-1 and IL-8 in response to bleomycin exposure. Bleomycin 91-100 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 26669014-15 2015 Raised levels of IL8 titers were also found in all 11 DHF patients. dhf 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 26669014-18 2015 Prediction efficacy of IL8, CIC and cryoglobulin for DHF was determined using the receiver operator characteristic curve (ROC). dhf 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 25820539-8 2015 MACs caused an increase in vessel formation in in vivo models through the production of IL-8. macs 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 26505478-11 2015 IL-17A promoted stabilization of CXCL8 mRNA in BEAS-2B cells treated with poly(I:C). poly 74-78 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 26395911-10 2015 RESULTS: In monolayer cultures of DPCs, L-MIM at nontoxic concentrations increased the production of VEGF and IL-8 in the presence of AGEs. Mimosine 40-45 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 26172313-6 2015 NO-np significantly suppressed IL-1beta, tumor necrosis factor-alpha (TNF-alpha), IL-8, and IL-6 from human monocytes, and IL-8 and IL-6 from human keratinocytes, respectively. Neptunium 3-5 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 26172313-6 2015 NO-np significantly suppressed IL-1beta, tumor necrosis factor-alpha (TNF-alpha), IL-8, and IL-6 from human monocytes, and IL-8 and IL-6 from human keratinocytes, respectively. Neptunium 3-5 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 26252749-8 2015 At specific times during healing, the azithromycin group exhibited significantly lower levels of interleukin (IL)-6 and IL-8 in GCF than the amoxicillin group and exhibited significantly lower levels of granulocyte colony stimulating factor, IL-8, macrophage inflammatory protein-1beta, and interferon-gamma-inducible protein-10 in PICF. Azithromycin 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 26252749-8 2015 At specific times during healing, the azithromycin group exhibited significantly lower levels of interleukin (IL)-6 and IL-8 in GCF than the amoxicillin group and exhibited significantly lower levels of granulocyte colony stimulating factor, IL-8, macrophage inflammatory protein-1beta, and interferon-gamma-inducible protein-10 in PICF. Azithromycin 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 242-246 26520736-3 2015 The authors aim to quantify and reduce the bias introduced by MRACnobone in the standard uptake value (SUV) of spinal and pelvic lesions in 20 PET/MRI examinations with [18F]NaF. mracnobone 62-72 C-X-C motif chemokine ligand 8 Homo sapiens 174-177 26520736-15 2015 The analysis of the 20 [18F]NaF PET/MRI examinations revealed relative SUVmax differences between PETnobone and PETbone of (-8.8%+-2.7%, p=0.01) and (-8.1%+-1.9%, p=2.4x10(-8)) in pelvic and spinal lesions, respectively. petnobone 98-107 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 26099791-9 2015 Hyperosmolar HES 200/0.5 and albumin showed significantly different pattern of recovery with increased concentration of MIG, IP-10, C3a and C5a and decreased concentration of IL-1beta, TNF, MCP-1 and IL-8 in comparison with dextran 60. Hydroxyethyl Starch Derivatives 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 26517722-8 2015 Dexamethasone suppression of the LPS-induced IL-8 mRNA production by steroid resistant asthmatics PBMC in the presence of p38 and ERK inhibitors was evaluated by real time PCR. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 26517722-8 2015 Dexamethasone suppression of the LPS-induced IL-8 mRNA production by steroid resistant asthmatics PBMC in the presence of p38 and ERK inhibitors was evaluated by real time PCR. Steroids 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 26160865-7 2015 Overexpression of miR-17 inhibited basal and agonist-induced IL-8 protein production in F508del-CFTR homozygous CFTE29o(-) tracheal, CFBE41o(-) and/or IB3 bronchial epithelial cells. f508del 88-95 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 26282378-0 2015 Induction of oxidative stress by Taxol vehicle Cremophor-EL triggers production of interleukin-8 by peripheral blood mononuclear cells through the mechanism not requiring de novo synthesis of mRNA. Paclitaxel 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 26282378-0 2015 Induction of oxidative stress by Taxol vehicle Cremophor-EL triggers production of interleukin-8 by peripheral blood mononuclear cells through the mechanism not requiring de novo synthesis of mRNA. cremophor EL 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 26535717-7 2015 The expression of NF-kappaBp65 and IL-8 in CSE-stimulated normal HBE cells was inhibited by 15d-PGJ2 at both the mRNA level and the protein level. 15-deoxy-delta(12,14)-prostaglandin J2 92-100 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 26517722-12 2015 P38 inhibitor significantly enhanced DEX suppression of LPS-induced IL-8 mRNA by PBMC of steroid resistant asthmatics. Dextromethorphan 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 26517722-12 2015 P38 inhibitor significantly enhanced DEX suppression of LPS-induced IL-8 mRNA by PBMC of steroid resistant asthmatics. Steroids 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 26543772-2 2015 This paper traces some aspects of this failure to a compensatory erlotinib-mediated increase in interleukin-8. Erlotinib Hydrochloride 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 26543772-6 2015 FINDINGS: The old sulfone antibiotic dapsone- one of the very first antibiotics in clinical use- has demonstrated several interleukin-8 system inhibiting actions. Sulfones 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 122-135 26543772-6 2015 FINDINGS: The old sulfone antibiotic dapsone- one of the very first antibiotics in clinical use- has demonstrated several interleukin-8 system inhibiting actions. Dapsone 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 122-135 26543772-8 2015 Erlotinib typically gives a rash that has recently been proven to come about via an erlotinib triggered up-regulated keratinocyte interleukin-8 synthesis. Erlotinib Hydrochloride 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 130-143 26543772-8 2015 Erlotinib typically gives a rash that has recently been proven to come about via an erlotinib triggered up-regulated keratinocyte interleukin-8 synthesis. Erlotinib Hydrochloride 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 130-143 26267317-0 2015 The role of interleukin-8 (IL-8) and IL-8 receptors in platinum response in high grade serous ovarian carcinoma. Platinum 55-63 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 26539118-9 2015 In addition, nuciferine decreased TNF-a, IL-6 and IL-8 as well as the siRNA PASK group. nuciferine 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 26160521-10 2015 Furthermore, a heptane-soluble (non-polar) extract of DEP induced both IL-6 and CXCL8 release, whereas a PBS-soluble (highly polar) extract induced only IL-6. Heptanes 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 26483408-9 2016 We show that the A subunit-dependent ERK1/2 activation is mediated through ZAK-dependent signaling, and inhibition of ERK1/2 activation via the MEK1/2 inhibitors U0126 and PD98059 results in decreased Stx1-mediated IL-8 mRNA. U 0126 162-167 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 26483408-9 2016 We show that the A subunit-dependent ERK1/2 activation is mediated through ZAK-dependent signaling, and inhibition of ERK1/2 activation via the MEK1/2 inhibitors U0126 and PD98059 results in decreased Stx1-mediated IL-8 mRNA. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 172-179 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 26854163-2 2015 Sodium (18)F-fluoride [(18)F]-NaF PET/CT was performed prior the treatment of (223)RaCl2, after the first cycle and after the sixth cycle. sodium (18)f-fluoride 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 26267317-3 2015 We studied the expression of IL-8 and IL-8 receptors in platinum sensitive and resistant cell lines. Platinum 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 26267317-3 2015 We studied the expression of IL-8 and IL-8 receptors in platinum sensitive and resistant cell lines. Platinum 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 26267317-4 2015 Using qRT-PCR and immunohistochemistry, both platinum sensitive (PEA1, PEO14) and resistant (PEA2, PEO23) show increased expression of IL-8 and IL-8 receptors. Platinum 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 26267317-4 2015 Using qRT-PCR and immunohistochemistry, both platinum sensitive (PEA1, PEO14) and resistant (PEA2, PEO23) show increased expression of IL-8 and IL-8 receptors. Platinum 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 26267317-6 2015 Knockdown of IL-8 increased sensitivity to cisplatin in platinum sensitive and reversed platinum resistance in resistant cell lines, decreased the expression of anti-apoptotic Bcl-2 and decreased inhibitory phosphorylation of pro-apoptotic Bad. Cisplatin 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 26267317-6 2015 Knockdown of IL-8 increased sensitivity to cisplatin in platinum sensitive and reversed platinum resistance in resistant cell lines, decreased the expression of anti-apoptotic Bcl-2 and decreased inhibitory phosphorylation of pro-apoptotic Bad. Platinum 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 26267317-6 2015 Knockdown of IL-8 increased sensitivity to cisplatin in platinum sensitive and reversed platinum resistance in resistant cell lines, decreased the expression of anti-apoptotic Bcl-2 and decreased inhibitory phosphorylation of pro-apoptotic Bad. Platinum 88-96 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 26267317-7 2015 IL-8 receptor antagonist treatment also enhanced platinum sensitivity. Platinum 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 26550541-1 2015 [(18)F] sodium fluoride (NaF) PET/CT is a current, clinically relevant method to assess bone metastases. Sodium Fluoride 8-23 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 26267317-9 2015 Inhibition of IL-8 signalling can enhance response in platinum sensitive and resistant disease. Platinum 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 26446923-9 2015 In comparison to the explants treated only with LPS, pre-treatment with 0.01-1.0 muM progesterone significantly blunted (73, 56, 56, 75, 25, 48 %) the secretion of TNF-alpha, IL-1beta, IL-6, IL-8, MIP-1alpha, IL-10, respectively. Progesterone 85-97 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 26455818-6 2015 H2S donors increased glutathione and superoxide dismutase in CS exposed U937 cells and inhibited CS-induced TNF-alpha and IL-8 secretion. Hydrogen Sulfide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 26202107-5 2015 Depot medroxyprogesterone acetate (DMPA) users had significantly higher MIP-1alpha, MIP-1beta, IL-6, IL-8, IP-10, and RANTES concentrations. Medroxyprogesterone Acetate 6-33 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 26284488-9 2015 The search for mediators of senescent HPMC activity showed that increased SW480 cell proliferation was stimulated by IL-6, migration by CXCL8 and CCL2, invasion by IL-6, MMP-3 and uPA, and epithelial-mesenchymal transition by TGF-beta1. Hypromellose Derivatives 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 136-141 26202107-5 2015 Depot medroxyprogesterone acetate (DMPA) users had significantly higher MIP-1alpha, MIP-1beta, IL-6, IL-8, IP-10, and RANTES concentrations. Medroxyprogesterone Acetate 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 25781052-7 2015 Data also revealed a reduction in MUC5AC, IL-6, and IL-8 expression levels in MAG-DHA-treated shCFTR cells stimulated, or not, with LPS. dehydroacetic acid 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 26202107-6 2015 Norethisterone oenanthate users had significantly higher IL-6, IL-8, and RANTES concentrations. norethindrone enanthate 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 26205304-1 2015 UNLABELLED: Sodium 18F-fluoride (18F-NaF) PET/CT imaging is a promising imaging technique for the assessment of atherosclerosis but is hampered by a lack of validated quantification protocols. SODIUM FLUORIDE F-18 12-31 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 25781052-9 2015 After MAG-DHA treatments, messenger RNA transcript levels for MUC5AC, IL-6, and IL-8 were markedly reduced in LPS-treated CFTR siRNA bronchi. docosahexaenoic acid monoacylglyceride 6-13 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 26341987-6 2015 Sputum interleukin (IL)-6 and growth-regulated oncogene (GRO)-alpha and serum GRO-alpha, IL-1ss and IL-8 levels increased with AZD5069 versus placebo (all p<0.001), while serum high-sensitivity C-reactive protein levels did not change. N-(2-(2,3-difluoro-6-benzylthio)-6-(3,4-dihydroxybutan-2-yloxy)pyrimidin-4-yl)azetidine-1-sulfonamide 127-134 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 26465888-11 2015 The expression levels of IL-6 and IL-8 were reduced when cells were seeded on graphene foam as compared to Ti and graphene film. Graphite 78-86 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 26465888-11 2015 The expression levels of IL-6 and IL-8 were reduced when cells were seeded on graphene foam as compared to Ti and graphene film. Graphite 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 26133961-2 2015 Ex vivo storage of PCs is associated with a storage lesion characterized by partial platelet activation and the release of soluble mediators, such as soluble CD40 ligand (sCD40L), RANTES, and interleukin (IL)-8. pcs 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 192-210 26740893-15 2015 Levocetirizine has a better effect on decreasing the symptoms and plasmatic levels of IL-1beta and IL-8. levocetirizine 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 26178144-0 2015 Down-regulation of IL-8 by high-dose vitamin D is specific to hyperinflammatory macrophages and involves mechanisms beyond up-regulation of DUSP1. Vitamin D 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 26178144-2 2015 Vitamin D transcriptionally up-regulates the anti-inflammatory gene DUSP1, which partly controls production of the inflammatory chemokine IL-8. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 26178144-4 2015 We tested the ability of vitamin D metabolites to down-regulate IL-8 production in CF macrophages. Vitamin D 25-34 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 26178144-10 2015 Vitamin D metabolites down-regulated stimulated IL-8 only in those hyperinflammatory MDM, and only when used at high doses (>100 nM for 25OHD3 , or >1 nM for 1,25(OH)2 D3 and paricalcitol). Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 26178144-10 2015 Vitamin D metabolites down-regulated stimulated IL-8 only in those hyperinflammatory MDM, and only when used at high doses (>100 nM for 25OHD3 , or >1 nM for 1,25(OH)2 D3 and paricalcitol). paricalcitol 181-193 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 26178144-11 2015 The magnitude of IL-8 down-regulation by vitamin D metabolites or paricalcitol was moderate (~30% vs. >70% by low-dose dexamethasone). Vitamin D 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 26178144-11 2015 The magnitude of IL-8 down-regulation by vitamin D metabolites or paricalcitol was moderate (~30% vs. >70% by low-dose dexamethasone). paricalcitol 66-78 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 26178144-11 2015 The magnitude of IL-8 down-regulation by vitamin D metabolites or paricalcitol was moderate (~30% vs. >70% by low-dose dexamethasone). Dexamethasone 122-135 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 26178144-13 2015 CONCLUSIONS AND IMPLICATIONS: Vitamin D metabolites and their analogues moderately down-regulate IL-8 in hyperinflammatory macrophages, including those from CF. Vitamin D 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 26194066-0 2015 House dust mite allergen Der f 1 induces IL-8 in human basophilic cells via ROS-ERK and p38 signal pathways. Reactive Oxygen Species 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 26194066-6 2015 The antioxidant N-acetyl-cysteine (NAC) inhibited phosphorylation of ERK, but not p38, suggesting that secretion of IL-8 in KU812 cells treated with Der f 1 is dependent on ROS, ERK MAPK and p38 MAPK. Acetylcysteine 16-33 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26194066-6 2015 The antioxidant N-acetyl-cysteine (NAC) inhibited phosphorylation of ERK, but not p38, suggesting that secretion of IL-8 in KU812 cells treated with Der f 1 is dependent on ROS, ERK MAPK and p38 MAPK. Acetylcysteine 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 25750008-11 2015 Compared with the control group, the hydrogen group had a statistically significantly lower expression of IL-1beta (P = 0.0317), IL-6 (P = 0.0159), IL-8 (P = 0.0195) and TNF-alpha (P = 0.0159). Hydrogen 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 26360022-0 2015 Correction: ZFC3H1, a Zinc Finger Protein, Modulates IL-8 Transcription by Binding with Celastramycin A, a Potential Immune Suppressor. celastramycin A 88-103 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 26180016-11 2015 Furthermore, IL-8 was significantly increased in IBS-D patients with a self-rating anxiety scale (SAS) or SDS score >=50 (P=0.016, P=0.008, respectively) as compared with that in patients scoring <50. sds 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 26321412-0 2015 Sphingosine 1-phosphate regulates IL-8 expression and secretion via S1PR1 and S1PR2 receptors-mediated signaling in extravillous trophoblast derived HTR-8/SVneo cells. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 26321412-4 2015 IL-8 also promotes trophoblast cell migration and invasion, and stimulates the secretion of progesterone. Progesterone 92-104 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 26321412-5 2015 The induction and mechanism of IL-8 secretion by EVT is still unknown. EVT 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 26321412-8 2015 RESULTS: We found that S1P induces IL-8 gene expression and protein secretion in EVT derived HTR-8/SVneo cells but not in BeWo cells. EVT 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 26321412-9 2015 SEW2781, the selective agonist of S1PR(1), induced IL-8 gene expression but not protein secretion. sew2781 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 26321412-10 2015 The specific S1PR(2) inhibitor JTE-013 could drastically inhibit IL-8 secretion. JTE 013 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 26321412-12 2015 Selective Rho-kinase inhibitor Y27632 and Rac1 inhibitor NSC23766 could block IL-8 secretion in these cells. Y 27632 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 26418032-6 2015 Inhibition of the TLR3, TLR/TIR-domain-containing adaptor-inducing interferon beta (TRIF), NF-kappaB, and IRF3 pathways decreased the polyI:C- and IL-17A/polyI:C-induced G-CSF and IL-8 mRNA expression. Poly I 134-139 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 26418032-6 2015 Inhibition of the TLR3, TLR/TIR-domain-containing adaptor-inducing interferon beta (TRIF), NF-kappaB, and IRF3 pathways decreased the polyI:C- and IL-17A/polyI:C-induced G-CSF and IL-8 mRNA expression. Poly I 154-159 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 26406307-11 2015 Glutathione depletion augmented CXCL8 responses by 1.49x (CI 1.02-2.17) compared with wood smoke alone. Glutathione 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 32-37 26397719-5 2015 T-oligos injected into the uteri of pregnant CD1 mice on day 14 of gestation, led to increased p38MAPK, SA-beta-gal (SA beta-gal) staining in murine amniotic sacs and higher AF IL-8 levels on day 18, compared to saline treated controls. 2',5'-oligoadenylate 1-8 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 26232645-10 2015 Administration of bilirubin reduced mean linear intercept and mean alveoli area, increased mean alveoli number, reduced macrophage, neutrophil and TNF-alpha content of BALF, and increased BALF and serum IL-10 level, but lowered local and systemic CCL2, CXCL2, CXCL8 and IL-17 levels. Bilirubin 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 260-265 26134265-4 2015 Pre-treatment of TQ inhibited TNF-alpha-induced interleukin-6 (IL-6) and IL-8 production and ICAM-1, VCAM-1, and cadherin-11 (Cad-11) expression in RA-FLS (p<0.01). thymoquinone 17-19 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 26360879-6 2015 Surprisingly, co-stimulation with PAF+SAF demonstrated that SAF strongly inhibited the PAF-driven IL-8 production, showing that SAF has potent anti-inflammatory effects. Syntex adjuvant formulation 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 26360879-6 2015 Surprisingly, co-stimulation with PAF+SAF demonstrated that SAF strongly inhibited the PAF-driven IL-8 production, showing that SAF has potent anti-inflammatory effects. Syntex adjuvant formulation 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 26360879-6 2015 Surprisingly, co-stimulation with PAF+SAF demonstrated that SAF strongly inhibited the PAF-driven IL-8 production, showing that SAF has potent anti-inflammatory effects. Platelet Activating Factor 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 26360879-6 2015 Surprisingly, co-stimulation with PAF+SAF demonstrated that SAF strongly inhibited the PAF-driven IL-8 production, showing that SAF has potent anti-inflammatory effects. Syntex adjuvant formulation 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 26758116-11 2015 (3) In steroid group, IL-2 and IL-8 in BALF of patient whose fever disappeared after steroid therapy were both significantly lower than that of patients who still had fever (t=2.771, 2.054, P=0.010, 0.049) , but no significant difference was found between the two groups in BALF IL-1 beta, IL-4, IL-6, IL-10, IFN-gamma levels (P>0.05). Steroids 7-14 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 26758116-11 2015 (3) In steroid group, IL-2 and IL-8 in BALF of patient whose fever disappeared after steroid therapy were both significantly lower than that of patients who still had fever (t=2.771, 2.054, P=0.010, 0.049) , but no significant difference was found between the two groups in BALF IL-1 beta, IL-4, IL-6, IL-10, IFN-gamma levels (P>0.05). Steroids 85-92 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 26758116-13 2015 (2) Incresed BALF IL-1 beta, IL-4, IL-6, IL-8, IL-10, IFN-gamma levels were observed in RMPP and high level of BALF IL-2 and IL-8 might have some relevance with persistent fever of RMPP in children. rmpp 88-92 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 26758116-13 2015 (2) Incresed BALF IL-1 beta, IL-4, IL-6, IL-8, IL-10, IFN-gamma levels were observed in RMPP and high level of BALF IL-2 and IL-8 might have some relevance with persistent fever of RMPP in children. rmpp 181-185 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 26418032-3 2015 In this study, we demonstrated that IL-17A and polyI:C, the ligand of TLR3, synergistically induced the expression of proinflammatory cytokines and chemokines (G-CSF, IL-8, CXCL1, CXCL5, IL-1F9), but not type I interferon (IFN-alpha1, -beta) in primary culture of normal human bronchial epithelial cells. Poly I-C 47-54 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 26407698-2 2015 Since SDF is not available in certain countries, some dentists use adjunctive application of 25 % silver nitrate (AgNO3) and 5 % sodium fluoride (NaF) to arrest ECC. Sodium Fluoride 129-144 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 26407698-13 2015 Lower concentrations of silver and fluoride are contained in 25 % AgNO3 and 5 % NaF, respectively, than in 38 % SDF; therefore, AgNO3/NaF are more favourable for use in young children. Silver 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 26407698-13 2015 Lower concentrations of silver and fluoride are contained in 25 % AgNO3 and 5 % NaF, respectively, than in 38 % SDF; therefore, AgNO3/NaF are more favourable for use in young children. Silver 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 26407698-13 2015 Lower concentrations of silver and fluoride are contained in 25 % AgNO3 and 5 % NaF, respectively, than in 38 % SDF; therefore, AgNO3/NaF are more favourable for use in young children. Fluorides 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 26407698-14 2015 Because its use for caries management is painless, simple, low-cost, and approved in many countries, AgNO3/NaF could be widely recommended and promoted as an alternative treatment to conventional invasive management of ECC. Silver Nitrate 101-106 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 26234943-0 2015 Synthetic heparan sulfate dodecasaccharides reveal single sulfation site interconverts CXCL8 and CXCL12 chemokine biology. heparan sulfate dodecasaccharides 10-43 C-X-C motif chemokine ligand 8 Homo sapiens 87-92 26283481-6 2015 Using cell lines and primary airway epithelial cells (both submerged and well-differentiated), we observed that pure poly(I:C) stimulated IFN-beta mainly through the TLR3/TRIF pathway and IL-8 through an unidentified pathway. poly 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 26283481-9 2015 In contrast, we show that stimulation of the RIG-I/MAVS pathway, such as when poly(I:C) is delivered intracellularly in a complex with liposomes or via nucleofection, selectively stimulates IFN-beta with low IL-8 costimulation. Poly I-C 78-87 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 26360879-5 2015 Immortalised airway epithelial cells (Beas-2B) exposed to bacteria-free filtrates from PA (PAF) induced a robust production of the neutrophil chemoattractant IL-8 while bacteria-free filtrates from SA (SAF) had a minimal effect. Platelet Activating Factor 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 26360879-5 2015 Immortalised airway epithelial cells (Beas-2B) exposed to bacteria-free filtrates from PA (PAF) induced a robust production of the neutrophil chemoattractant IL-8 while bacteria-free filtrates from SA (SAF) had a minimal effect. Syntex adjuvant formulation 202-205 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 26360879-6 2015 Surprisingly, co-stimulation with PAF+SAF demonstrated that SAF strongly inhibited the PAF-driven IL-8 production, showing that SAF has potent anti-inflammatory effects. Platelet Activating Factor 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 26340264-7 2015 The adipose tissue and placenta of treated women exhibited a significant decrease in TLR4 adipose and placental expression as well as IL6, IL8, and TNFalpha In vitro, EPA and DHA suppressed the activation of TLR4, IL6, IL8 induced by palmitate in culture of adipose and trophoblast cells. Eicosapentaenoic Acid 167-170 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 26252471-2 2015 Here we provide evidence that 2-electron reduction of a (formazanate)BF2 precursor leads to NaF elimination and formation of an N-heterocyclic boron carbenoid, and describe the formation of a series of unusual BN heterocycles that result from trapping of this fragment. (formazanate)bf2 56-72 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 26333527-7 2015 IL-6, IL-8, IL-1beta and TNF-alpha concentration in NBL showed inverse correlation coefficients with the peroxidation products of fatty acids. Fatty Acids 130-141 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 26340264-7 2015 The adipose tissue and placenta of treated women exhibited a significant decrease in TLR4 adipose and placental expression as well as IL6, IL8, and TNFalpha In vitro, EPA and DHA suppressed the activation of TLR4, IL6, IL8 induced by palmitate in culture of adipose and trophoblast cells. Eicosapentaenoic Acid 167-170 C-X-C motif chemokine ligand 8 Homo sapiens 219-222 26255641-10 2015 As compared to the diffusivity of Li in other common inorganic SEI compounds, such as Li2CO3 and Li2O, the cation diffusivity in LiF and NaF is quite low, with at least three orders of magnitude lower ionic conductivities. Lithium Carbonate 86-92 C-X-C motif chemokine ligand 8 Homo sapiens 137-140 26340264-7 2015 The adipose tissue and placenta of treated women exhibited a significant decrease in TLR4 adipose and placental expression as well as IL6, IL8, and TNFalpha In vitro, EPA and DHA suppressed the activation of TLR4, IL6, IL8 induced by palmitate in culture of adipose and trophoblast cells. Docosahexaenoic Acids 175-178 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 26340264-7 2015 The adipose tissue and placenta of treated women exhibited a significant decrease in TLR4 adipose and placental expression as well as IL6, IL8, and TNFalpha In vitro, EPA and DHA suppressed the activation of TLR4, IL6, IL8 induced by palmitate in culture of adipose and trophoblast cells. Docosahexaenoic Acids 175-178 C-X-C motif chemokine ligand 8 Homo sapiens 219-222 25894228-11 2015 Concomitant treatment of SZ95 sebocytes with APS attenuated the effect of IL-1beta and TNF-alpha on IL-6 and IL-8 gene expression as well as on IL-1beta-mediated NF-kappaB signaling. aps 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 26665398-0 2015 THE EFFECT OF SULFASALAZINE AND 5-AMINOSALICYLIC ACID ON THE SECRETION OF INTERLEUKIN 8 BY HUMAN COLON MYOFIBROBLASTS. Sulfasalazine 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 26665398-0 2015 THE EFFECT OF SULFASALAZINE AND 5-AMINOSALICYLIC ACID ON THE SECRETION OF INTERLEUKIN 8 BY HUMAN COLON MYOFIBROBLASTS. Mesalamine 32-53 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 25894228-6 2015 Here, we investigated if APS attenuates IL-1beta- or TNF-alpha-mediated IL-6 and IL-8 expression in SZ95 sebocytes, whereas TNF-alpha was used as control. aps 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 26072364-13 2015 Our results demonstrate that changes in HA morphology and carbonate content influence breast cancer cell growth and interleukin-8 secretion, and suggest that characterizing the effect of HA properties on breast cancer cells may improve our understanding of breast cancer development and progression. Carbonates 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 25582838-3 2015 As a readout for receptor signaling, we observe the dynamics of calcium release in neutrophils following contact with the IL-8 coated surface. Calcium 64-71 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 26136104-6 2015 The results revealed that treatment with YCG063 significantly inhibited the levels of IL-6, IL-8, MCP-1 and ICAM-1 in the PA-LPS-stimulated ARPE-19 cells. YCG 063 41-47 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 26845056-10 2015 Furthermore, IL-8 and IL-25 levels are decreased following treatment with prednisone acetate. Nisone 74-92 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 26202921-10 2015 MAIN RESULTS AND THE ROLE OF CHANCE: The long chain saturated fatty acids, stearic and palmitic (PA), stimulated the synthesis as well as the release of TNF-alpha, IL-6 and IL-8 by trophoblast cells (2- to 6-fold, P < 0.001). long chain saturated fatty acids 41-73 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 26202921-10 2015 MAIN RESULTS AND THE ROLE OF CHANCE: The long chain saturated fatty acids, stearic and palmitic (PA), stimulated the synthesis as well as the release of TNF-alpha, IL-6 and IL-8 by trophoblast cells (2- to 6-fold, P < 0.001). stearic 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 26202921-10 2015 MAIN RESULTS AND THE ROLE OF CHANCE: The long chain saturated fatty acids, stearic and palmitic (PA), stimulated the synthesis as well as the release of TNF-alpha, IL-6 and IL-8 by trophoblast cells (2- to 6-fold, P < 0.001). Protactinium 97-99 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 26143497-8 2015 Also, galactose disrupted this inhibition on the expression of IL-8 and hBD-2. Galactose 6-15 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 25726004-3 2015 So, we conducted this study with the purpose of investigating the effect of sodium fluoride (NaF) in human RPMI8226 cells. Sodium Fluoride 76-91 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 25982554-4 2015 When the human intestinal epithelial cell-line, Caco-2, and the primary colon cells were stimulated with ethanol-inactivated S. aureus, IL-8 expression was induced in a dose-dependent manner. Ethanol 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 26400525-9 2015 CONCLUSIONS: Clinical efficacy of TACE and patient survival in liver cancer are associated with specific variants of IL-8 and IL-10 genes. Chlorotrianisene 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 25977183-6 2015 Moreover, pretreatment of NHEKs with Z-lig reduced UVB-induced nuclear factor kappa B (NF-kappaB)-dependent inflammatory mediators (IL-6, IL-8 and MCP-1) production at both mRNA and protein level. ligustilide 37-42 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 25828268-12 2015 MitoQ and Tiron inhibited TGF-beta-induced ASM cell proliferation and CXCL8 release. mitoquinone 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 70-75 26617775-4 2015 We observed in HK-2 cells that fenofibrate significantly inhibited fatty acids bound albumin (FA-BSA) induced up-regulation of MCP-1 and IL-8. Fenofibrate 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 26617775-4 2015 We observed in HK-2 cells that fenofibrate significantly inhibited fatty acids bound albumin (FA-BSA) induced up-regulation of MCP-1 and IL-8. Fatty Acids 67-78 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 25828268-12 2015 MitoQ and Tiron inhibited TGF-beta-induced ASM cell proliferation and CXCL8 release. 1,2-Dihydroxybenzene-3,5-Disulfonic Acid Disodium Salt 10-15 C-X-C motif chemokine ligand 8 Homo sapiens 70-75 26044852-5 2015 RESULTS: Inhibition of LPS-induced CXCL8 and TNF-alpha expression by IL-10 proceeds through a common mechanism targeting LPS-induced phosphorylation of the nuclear factor kappaB p65 serine 276 residue (pS276p65). Serine 182-188 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 25754990-0 2015 Inhibition of PKC-Induced COX-2 and IL-8 Expression in Human Breast Cancer Cells by Glucosamine. Glucosamine 84-95 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 25689957-0 2015 IL-1ss and IL-8 are scavenged by the hexadecylamide derivative of hyaluronic acid: a new mechanism. hexadecylamide 37-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-15 25689957-0 2015 IL-1ss and IL-8 are scavenged by the hexadecylamide derivative of hyaluronic acid: a new mechanism. Hyaluronic Acid 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 0-15 25754990-5 2015 In MCF-7 breast cancer cells, glucosamine effectively suppresses the PKC induction of COX-2 and IL-8 promoter activity, mRNA and protein levels, as well as the production of prostaglandin E(2) (PGE(2)) and IL-8. Glucosamine 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 25754990-4 2015 The aim of this study was to clarify the role and acting mechanism of glucosamine during the PKC-regulation of COX-2/IL-8 expression and the associated impact on breast cancer. Glucosamine 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 25754990-5 2015 In MCF-7 breast cancer cells, glucosamine effectively suppresses the PKC induction of COX-2 and IL-8 promoter activity, mRNA and protein levels, as well as the production of prostaglandin E(2) (PGE(2)) and IL-8. Glucosamine 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 26202982-8 2015 SYK kinase and the adaptor protein CARD9 were essential for glycolipid-induced IL-8 production. Glycolipids 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 25754990-10 2015 Furthermore, glucosamine significantly inhibits the growth of breast cancer xenografts and this is accompanied by a reduction in COX-2 and IL-8 expression. Glucosamine 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 24888491-0 2015 Alpha-mangostin suppresses IL-6 and IL-8 expression in P. gingivalis LPS-stimulated human gingival fibroblasts. mangostin 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 26426613-10 2015 Levels of IL-6, IL-1beta, and IL-8 detected in NPA from RSV single and associated to HRV were significantly higher than HRV infected and positively associated with days requiring O2.Levels of IL-6, IL-1beta, and IL-8 detected in NPA from patients infected with RSV only or with both RSV and HRV are increased, and any of those 3 cytokines may have a predictive value for the number of days with need of supplemental oxygen. Oxygen 179-181 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 25876063-5 2015 Osthole was able to suppress the levels of proinflammatory cytokines interleukin (IL)-1beta and IL-6, as well as chemokines monocyte chemoattractant protein-1 and IL-8. osthol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 26024755-0 2015 Niacin inhibits fat accumulation, oxidative stress, and inflammatory cytokine IL-8 in cultured hepatocytes: Impact on non-alcoholic fatty liver disease. Niacin 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 26024755-7 2015 Niacin reduced palmitic acid-induced IL-8 levels. Niacin 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 26024755-7 2015 Niacin reduced palmitic acid-induced IL-8 levels. Palmitic Acid 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 26024755-9 2015 Decreased ROS production, at least in part, may have contributed to the inhibition of pro-inflammatory IL-8 levels. Reactive Oxygen Species 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 24888491-1 2015 This study aims to investigate the effect of alpha-mangostin on interleukin (IL)-6 and IL-8 expression in human gingival fibroblasts (HGFs). mangostin 45-60 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 24888491-5 2015 Alpha-mangostin reduced IL-6 and IL-8 mRNA and protein in P. gingivalis LPS-stimulated HGFs. mangostin 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 26008221-0 2015 Arsenic exposure causes epigenetic dysregulation of IL-8 expression leading to proneoplastic changes in kidney cells. Arsenic 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 26032617-3 2015 Molecular imaging using (18)F-sodium fluoride ((18)F-NaF) positron emission tomography (PET)/computed tomography (CT) has been recently proposed as a marker to study the in vivo mineralization process in the atheroma plaque. Sodium Fluoride 30-45 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 26008221-3 2015 In this work, we have studied the effect of arsenic exposure on renal system using human embryonic kidney cells and prenatally exposed animals and identified Interleukin-8(IL-8) and its homologue (CINC-1) as mediators of arsenic induced renal toxicity. Arsenic 221-228 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 26008221-3 2015 In this work, we have studied the effect of arsenic exposure on renal system using human embryonic kidney cells and prenatally exposed animals and identified Interleukin-8(IL-8) and its homologue (CINC-1) as mediators of arsenic induced renal toxicity. Arsenic 221-228 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 26008221-4 2015 We further show that embryonic kidney cells are more responsive to arsenic leading to higher induction of IL-8 as compared to adult cells due to DNA methylation and histone acetylation (H3 acetylation) changes in the IL-8 promoter. Arsenic 67-74 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 26008221-4 2015 We further show that embryonic kidney cells are more responsive to arsenic leading to higher induction of IL-8 as compared to adult cells due to DNA methylation and histone acetylation (H3 acetylation) changes in the IL-8 promoter. Arsenic 67-74 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 26008221-5 2015 Through bisulfite analysis of the IL-8 promoter, we have also identified an arsenic modulated CpG site at -168 bases upstream of transcription start site. hydrogen sulfite 8-17 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 26008221-5 2015 Through bisulfite analysis of the IL-8 promoter, we have also identified an arsenic modulated CpG site at -168 bases upstream of transcription start site. Arsenic 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 26008221-6 2015 This CpG is associated with C/EBP and CREB binding sites in the IL-8 promoter and its demethylation by arsenic coupled with increased H3 histone acetylation and CBP/P300 recruitment could lead to induction of IL-8. Arsenic 103-110 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 26008221-6 2015 This CpG is associated with C/EBP and CREB binding sites in the IL-8 promoter and its demethylation by arsenic coupled with increased H3 histone acetylation and CBP/P300 recruitment could lead to induction of IL-8. Arsenic 103-110 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 26008221-7 2015 Our study shows how epigenetic modulation of IL-8 by arsenic could contribute to increased cell migratory and proliferative capabilities, cell cycle dysregulation and renal toxicity. Arsenic 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 26269716-6 2015 We found that IL6, TNF, CXCL8, IL1B and ERK1/2 were the top genes in terms of the number of connections in platinum-induced neuropathy and TP53, MYC, PARP1, P38 MAPK and TNF for combined taxane-platinum-induced neuropathy. Platinum 107-115 C-X-C motif chemokine ligand 8 Homo sapiens 24-29 26215482-2 2015 Herein, we have investigated the effect of specific monovalent Hofmeister salts (NaH2PO4, NaF, NaCl, NaClO4, and NaSCN) on the coil-globule transition of poly(N-isopropylacrylamide) (PNIPAM) in a crowded macromolecular environment as a model for understanding the specific-ion effect on the solubility and stability of proteins in a crowded macromolecular environment. poly-N-isopropylacrylamide 154-181 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 26215482-3 2015 It was found that although the salts (NaH2PO4, NaF, and NaCl) and the macromolecular crowder (polyethylene glycol) lowered the transition temperature almost independently, the macromolecular crowder had a great impact on the transition temperature in the case of the chaotropes (NaClO4 and NaSCN). sodium perchlorate 279-285 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 26215482-3 2015 It was found that although the salts (NaH2PO4, NaF, and NaCl) and the macromolecular crowder (polyethylene glycol) lowered the transition temperature almost independently, the macromolecular crowder had a great impact on the transition temperature in the case of the chaotropes (NaClO4 and NaSCN). sodium thiocyanate 290-295 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 26269716-6 2015 We found that IL6, TNF, CXCL8, IL1B and ERK1/2 were the top genes in terms of the number of connections in platinum-induced neuropathy and TP53, MYC, PARP1, P38 MAPK and TNF for combined taxane-platinum-induced neuropathy. taxane 187-193 C-X-C motif chemokine ligand 8 Homo sapiens 24-29 26269716-6 2015 We found that IL6, TNF, CXCL8, IL1B and ERK1/2 were the top genes in terms of the number of connections in platinum-induced neuropathy and TP53, MYC, PARP1, P38 MAPK and TNF for combined taxane-platinum-induced neuropathy. Platinum 194-202 C-X-C motif chemokine ligand 8 Homo sapiens 24-29 26079696-7 2015 Moreover, we detected increased levels of interleukin (IL)-6 and IL-8 released in the 3 aldehyde exposure groups. Aldehydes 88-96 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 26086093-0 2015 27-Oxygenated cholesterol induces expression of CXCL8 in macrophages via NF-kappaB and CD88. Cholesterol 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 48-53 26086093-1 2015 We attempted to determine the effects of a milieu rich in cholesterol molecules on expression of chemokine CXCL8. Cholesterol 58-69 C-X-C motif chemokine ligand 8 Homo sapiens 107-112 26086093-2 2015 A high-cholesterol diet led to an increased transcription of the IL-8 gene in the arteries and elevated levels of CXCL8 in sera of ApoE(-/-) mice, compared with those of wild-type C57BL/6 mice. Cholesterol 7-18 C-X-C motif chemokine ligand 8 Homo sapiens 114-119 26086093-3 2015 Treatment of THP-1 monocyte/macrophage cells with 27-hydroxycholesterol (27OHChol) resulted in transcription of the IL-8 gene and increased secretion of its corresponding gene product whereas cholesterol did not induce expression of CXCL8 in THP-1 cells. 27-hydroxycholesterol 50-71 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26086093-3 2015 Treatment of THP-1 monocyte/macrophage cells with 27-hydroxycholesterol (27OHChol) resulted in transcription of the IL-8 gene and increased secretion of its corresponding gene product whereas cholesterol did not induce expression of CXCL8 in THP-1 cells. 27ohchol 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26086093-3 2015 Treatment of THP-1 monocyte/macrophage cells with 27-hydroxycholesterol (27OHChol) resulted in transcription of the IL-8 gene and increased secretion of its corresponding gene product whereas cholesterol did not induce expression of CXCL8 in THP-1 cells. Cholesterol 60-71 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26086093-3 2015 Treatment of THP-1 monocyte/macrophage cells with 27-hydroxycholesterol (27OHChol) resulted in transcription of the IL-8 gene and increased secretion of its corresponding gene product whereas cholesterol did not induce expression of CXCL8 in THP-1 cells. Cholesterol 60-71 C-X-C motif chemokine ligand 8 Homo sapiens 233-238 26086093-4 2015 27OHChol-induced transcription of the IL-8 gene was blocked by cycloheximide, but not by polymyxin B. 27ohchol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 26086093-4 2015 27OHChol-induced transcription of the IL-8 gene was blocked by cycloheximide, but not by polymyxin B. Cycloheximide 63-76 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 26086093-6 2015 Inhibition of NF-kappaB and CD88 using SN50 and W-54011, respectively, resulted in reduced transcription of the IL-8 gene and attenuated secretion of CXCL8 induced by 27OHChol. 27ohchol 167-175 C-X-C motif chemokine ligand 8 Homo sapiens 150-155 26086093-7 2015 We propose that oxidatively modified cholesterol like 27OHChol, rather than cholesterol, is responsible for sustained expression of CXCL8 in monocytes/macrophages in atherosclerotic arteries. Cholesterol 37-48 C-X-C motif chemokine ligand 8 Homo sapiens 132-137 26086093-7 2015 We propose that oxidatively modified cholesterol like 27OHChol, rather than cholesterol, is responsible for sustained expression of CXCL8 in monocytes/macrophages in atherosclerotic arteries. 27ohchol 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 132-137 26047642-5 2015 Conditioned medium from BK treated HASMC induced CXCL8, VEGF, and COX-2 mRNA and protein accumulation in airway epithelial cells, which were blocked by anti-amphiregulin antibodies and amphiregulin siRNA, suggesting a paracrine effect of HASMC-derived amphiregulin on airway epithelial cells. hasmc 35-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-54 26047642-8 2015 Our study provides evidence of a dynamic axis of interaction between HASMC and epithelial cells that amplifies CXCL8, VEGF, COX-2, and amphiregulin production. hasmc 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 111-116 25797323-9 2015 CRP, 8-isoprostane and LTB4 levels in serum, and IL-8 concentration in EBC correlated negatively with the value of forced expiratory volume in one second. NSC638702 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 26002274-1 2015 A fully automated production of the imaging agent sodium [(18)F]fluoride ([(18)F]NaF) on two different modules commercialized by Trasis , the AllInOne and the miniAllInOne, is reported. sodium [(18)f]fluoride 50-72 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 25891413-6 2015 RV1088 was also significantly more effective at inhibiting IL-6 and IL-8 production by monocytes and RA synovial fibroblasts compared with Humira. RV1088 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 25891413-7 2015 Finally, RV1088 was the only inhibitor that was effective in reducing TNF-alpha, IL-6 and IL-8 synthesis in RA synovial membrane cells with low nM IC50 s. CONCLUSIONS AND IMPLICATIONS: This study demonstrates potent anti-inflammatory effect of RV1088, highlighting that distinct signalling pathways drive TNF-alpha, IL-6 and IL-8 production in the different cell types found in RA joints. RV1088 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 25891413-7 2015 Finally, RV1088 was the only inhibitor that was effective in reducing TNF-alpha, IL-6 and IL-8 synthesis in RA synovial membrane cells with low nM IC50 s. CONCLUSIONS AND IMPLICATIONS: This study demonstrates potent anti-inflammatory effect of RV1088, highlighting that distinct signalling pathways drive TNF-alpha, IL-6 and IL-8 production in the different cell types found in RA joints. RV1088 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 325-329 26179154-4 2015 In early (first-third) passages, IL-6 and IL-8 concentration was higher at 20% O2 and in late (8th-12th) passages under 5% O2. Oxygen 79-81 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 26179154-4 2015 In early (first-third) passages, IL-6 and IL-8 concentration was higher at 20% O2 and in late (8th-12th) passages under 5% O2. Oxygen 123-125 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 25898227-8 2015 Long-term exposure to NOx was associated with decreased levels of interleukin (IL)-2, IL-8, IL-10 and tumor necrosis factor-alpha in Italy, but not in Sweden. Nitrogen Oxides 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 25898227-10 2015 Combining data from Italy and Sweden we only observed a significant association between long-term exposure to NOx and decreased levels of circulating IL-8. Nitrogen Oxides 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 26102216-6 2015 Our results show that the water extract from red vine leaves inhibits TNFalpha-induced IL-8 secretion and expression in human gastric epithelial cells; the effect should be maintained, although to a lesser extent, after gastric digestion. Water 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 26102216-9 2015 Our findings suggest that PFS containing water extracts from Vitis vinifera L. leaves could be useful to inhibit/attenuate gastric inflammation inhibiting IL-8 secretion and expression through impairment of the NF-kappaB pathway. Water 41-46 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 26190093-4 2015 Resveratrol can both decrease the secretion of proinflammatory cytokines (e.g., IL-6, IL-8, and TNF-alpha) and increase the production of anti-inflammatory cytokines; it also decreases the expression of adhesion proteins (e.g., ICAM-1) and leukocyte chemoattractants (e.g., MCP-1). Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 26349982-4 2015 Mechanistic studies revealed that BDMC-A might have exerted its activity by inhibiting metastatic and angiogenic pathways by modulating the expression of proteins upstream to NF-kappaB (TGF-beta, TNF-alpha, IL-1beta and c-Src), and NF-kappaB signaling cascade (c-Rel, COX-2, MMP-9, VEGF, IL-8) and by upregulating TIMP-2 levels. BDMC-A 34-40 C-X-C motif chemokine ligand 8 Homo sapiens 288-292 26672320-5 2015 The results show that trace fluoride phase mainly includes NaF, KF, CaF2, K2SiF6, Na2SiF6, Na3AlF6, K3AlF6, AlF3 3H2O, AlF2.3(OH)0.7 H2O, Ca5(PO4)3F, Ca10(PO4)6F2. Fluorides 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 25962642-9 2015 Within 2-4 h, Ag increased superoxide anion release and stimulated cytokine production (MCP-1, IL-8) that was diminished by Ca2+ inhibitors or trolox. 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid 143-149 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 26244291-6 2015 Sorafenib significantly inhibited production of TGF-beta1, VEGF, IL-6, IL-8, MCP-1, and TNF-alpha and blocked the activation of migration-related signaling molecules, such as HIF-1alpha, p-STAT3, MMP2, and Ang-1. Sorafenib 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 25503516-2 2015 Interleukin 8 (IL-8) released from macrophages is a key chemokine during initiation and progression of CS-induced lung inflammation, yet its regulation is largely unknown. Cesium 103-105 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 25503516-2 2015 Interleukin 8 (IL-8) released from macrophages is a key chemokine during initiation and progression of CS-induced lung inflammation, yet its regulation is largely unknown. Cesium 103-105 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 25503516-4 2015 Here we report that CS extract (CSE) increased the level of intracellular reactive oxygen species (ROS), activating AMPK, mitogen-activated protein kinases (MAPKs), and NF-kappaB, as well as inducing IL-8, in human macrophages. Cesium 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 25503516-5 2015 N-acetyl-cysteine (ROS scavenger) or hexamethonium [nicotinic acetylcholine receptor (nAChR) antagonist] attenuated the CSE-induced increase in intracellular ROS, activation of AMPK and NF-kappaB, as well as IL-8 induction, which suggests that nAChRs and ROS are important. Acetylcysteine 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 25503516-5 2015 N-acetyl-cysteine (ROS scavenger) or hexamethonium [nicotinic acetylcholine receptor (nAChR) antagonist] attenuated the CSE-induced increase in intracellular ROS, activation of AMPK and NF-kappaB, as well as IL-8 induction, which suggests that nAChRs and ROS are important. Reactive Oxygen Species 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 25503516-5 2015 N-acetyl-cysteine (ROS scavenger) or hexamethonium [nicotinic acetylcholine receptor (nAChR) antagonist] attenuated the CSE-induced increase in intracellular ROS, activation of AMPK and NF-kappaB, as well as IL-8 induction, which suggests that nAChRs and ROS are important. Hexamethonium 37-50 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 25503516-5 2015 N-acetyl-cysteine (ROS scavenger) or hexamethonium [nicotinic acetylcholine receptor (nAChR) antagonist] attenuated the CSE-induced increase in intracellular ROS, activation of AMPK and NF-kappaB, as well as IL-8 induction, which suggests that nAChRs and ROS are important. Reactive Oxygen Species 158-161 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 25503516-5 2015 N-acetyl-cysteine (ROS scavenger) or hexamethonium [nicotinic acetylcholine receptor (nAChR) antagonist] attenuated the CSE-induced increase in intracellular ROS, activation of AMPK and NF-kappaB, as well as IL-8 induction, which suggests that nAChRs and ROS are important. Reactive Oxygen Species 158-161 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 25822580-4 2015 Co-stimulation with IFN-gamma and the TLR3 ligand poly (I:C) synergistically increased the expression of IFN-beta, IL-6, IL-8, and human beta-defensin-2 in NHEKs compared with poly (I:C) or IFN-gamma alone. poly 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 25822580-4 2015 Co-stimulation with IFN-gamma and the TLR3 ligand poly (I:C) synergistically increased the expression of IFN-beta, IL-6, IL-8, and human beta-defensin-2 in NHEKs compared with poly (I:C) or IFN-gamma alone. Iodine 20-21 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 25822580-4 2015 Co-stimulation with IFN-gamma and the TLR3 ligand poly (I:C) synergistically increased the expression of IFN-beta, IL-6, IL-8, and human beta-defensin-2 in NHEKs compared with poly (I:C) or IFN-gamma alone. Carbon 0-1 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 25817444-7 2015 Targeting these newly identified signals, including AR, IL8, or miRNA32, may help us to better suppress PCa NE differentiation that is induced during ADT with anti-androgen enzalutamide (or casodex) treatment. enzalutamide 173-185 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 25817444-7 2015 Targeting these newly identified signals, including AR, IL8, or miRNA32, may help us to better suppress PCa NE differentiation that is induced during ADT with anti-androgen enzalutamide (or casodex) treatment. bicalutamide 190-197 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 25840438-0 2015 Enterococcus faecalis lipoteichoic acid suppresses Aggregatibacter actinomycetemcomitans lipopolysaccharide-induced IL-8 expression in human periodontal ligament cells. lipoteichoic acid 22-39 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 26117190-6 2015 The expression of interleukin-8 (IL-8) from Calu-3 induced with tumor necrosis factor alpha (TNF-alpha), transforming growth factor beta (TGF-beta1) and lipopolysaccharide (LPS) were significantly reduced after treatment with spray-dried resveratrol. Resveratrol 238-249 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 26117190-6 2015 The expression of interleukin-8 (IL-8) from Calu-3 induced with tumor necrosis factor alpha (TNF-alpha), transforming growth factor beta (TGF-beta1) and lipopolysaccharide (LPS) were significantly reduced after treatment with spray-dried resveratrol. Resveratrol 238-249 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 25503516-8 2015 Additionally, exposure of human macrophages to nicotine activated AMPK and induced IL-8 and that these effects were lessened by hexamethonium or compound C, implying that nicotine in CS may be causative. Nicotine 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 25503516-10 2015 Thus, we identified a novel nAChRs-dependent, ROS-sensitive, AMPK/MAPKs/NF-kappaB signaling pathway, which seems to be important to CS-induced macrophage IL-8 production and possibly to lung inflammation. nachrs 28-34 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 25503516-10 2015 Thus, we identified a novel nAChRs-dependent, ROS-sensitive, AMPK/MAPKs/NF-kappaB signaling pathway, which seems to be important to CS-induced macrophage IL-8 production and possibly to lung inflammation. Reactive Oxygen Species 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 25503516-10 2015 Thus, we identified a novel nAChRs-dependent, ROS-sensitive, AMPK/MAPKs/NF-kappaB signaling pathway, which seems to be important to CS-induced macrophage IL-8 production and possibly to lung inflammation. Cesium 132-134 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 26436037-14 2015 The Fluoride re release was high when recharging with professional regime (2% NaF) as compared to home regime (Toothpaste). Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 25954992-6 2015 The release of IL-8 from the A549 cells was assessed following treatment with EtP (2.5-10 mM), sodium pyruvate (NaP; 10 mM) or EtOH (85-170 mM) for 1, 24 or 72 h, prior to and following IL-6 stimulation. ethyl pyruvate 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 25954992-6 2015 The release of IL-8 from the A549 cells was assessed following treatment with EtP (2.5-10 mM), sodium pyruvate (NaP; 10 mM) or EtOH (85-170 mM) for 1, 24 or 72 h, prior to and following IL-6 stimulation. SODIUM PYRUVATE 95-110 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 25954992-6 2015 The release of IL-8 from the A549 cells was assessed following treatment with EtP (2.5-10 mM), sodium pyruvate (NaP; 10 mM) or EtOH (85-170 mM) for 1, 24 or 72 h, prior to and following IL-6 stimulation. N-(4-aminophenethyl)spiroperidol 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 25954992-6 2015 The release of IL-8 from the A549 cells was assessed following treatment with EtP (2.5-10 mM), sodium pyruvate (NaP; 10 mM) or EtOH (85-170 mM) for 1, 24 or 72 h, prior to and following IL-6 stimulation. Ethanol 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 25954992-8 2015 Treatment of the A549 cells with either EtOH or EtP significantly reduced the IL-6-induced release of IL-8. Ethanol 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 25954992-8 2015 Treatment of the A549 cells with either EtOH or EtP significantly reduced the IL-6-induced release of IL-8. ethyl pyruvate 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 25937253-14 2015 Consistent with the results of in vivo experiment, piscroside C significantly inhibited the expression of inflammatory cytokines (IL-6, IL-8 and IL-1beta) by inhibiting NF-kappaB activation, as resulting decrease in the phosphorylation of IKKbeta, IkappaBalpha and TAK1 in TNF-alpha-stimulated H292 cells. piscroside C 51-63 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 26207385-9 2015 Vitamin D inhibited TNFalpha-induced IL8 protein secretion levels to a comparable degree in fatal asthma- and non-asthma-derived ASM even though IL8 had significantly higher baseline levels in fatal asthma-derived ASM. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 26079480-5 2015 Trp-His inhibited interleukin (IL)-8 secretion in tumor necrosis factor (TNF)-alpha-stimulated HT-29 cells. tryptophyl-histidine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 18-36 26196332-7 2015 In conclusion, perioperative adjunctive use of dexmedetomidine substantially decreases serum IL-6, IL-8 and TNF-alpha levels. Dexmedetomidine 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 26668998-7 2015 In vitro, levels of AMPKalpha phosphorylation in phorbol-12- myristate-13-acetate (PMA) differentiated THP-1 cells was detected by immunohistochemistry, IL-8 level in supernatants of cigarette smoke condensate stimulating PMA differentiated THP-1 cells was measured by ELISA. Tetradecanoylphorbol Acetate 49-81 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 26182292-2 2015 Our previous studies have proved that activation of P2Y2 receptor by extracellular ATP could promote prostate cancer cell invasion and metastasis in vitro and in vivo via regulating the expressions of some epithelial-mesenchymal transition/invasion-related genes (including IL-8, E-cadherin, Snail and Claudin-1), and the most significant change in expression of IL-8 was observed after P2Y2 receptor activation. Adenosine Triphosphate 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 274-278 26182292-2 2015 Our previous studies have proved that activation of P2Y2 receptor by extracellular ATP could promote prostate cancer cell invasion and metastasis in vitro and in vivo via regulating the expressions of some epithelial-mesenchymal transition/invasion-related genes (including IL-8, E-cadherin, Snail and Claudin-1), and the most significant change in expression of IL-8 was observed after P2Y2 receptor activation. Adenosine Triphosphate 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 363-367 26182292-6 2015 Further experiments showed that inactivation of EGFR and ERK1/2 attenuated ATP-induced invasion and migration, and suppressed ATP-mediated IL-8 production. Adenosine Triphosphate 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 26182292-7 2015 In addition, knockdown of IL-8 inhibited ATP-mediated invasion and migration of prostate cancer cells. Adenosine Triphosphate 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 26151378-3 2015 Positron emission tomography and X-ray computed tomography (PET/CT) imaging of atherosclerosis using (18)F-sodium fluoride ((18)F-NaF) has the potential to identify pathologically high-risk nascent microcalcification. Sodium Fluoride 107-122 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 26138903-8 2015 Honokiol showed an anti-inflammatory effect in PA-inducted HUVECs by significantly inhibiting the generation of interleukin-6 (IL-6), IL-8 and monocyte chemoattractant protein-1. honokiol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 26138903-8 2015 Honokiol showed an anti-inflammatory effect in PA-inducted HUVECs by significantly inhibiting the generation of interleukin-6 (IL-6), IL-8 and monocyte chemoattractant protein-1. Palmitic Acid 47-49 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 26133108-8 2015 (iv) The reactive oxygen species (ROS) H2O2 (hydrogen peroxide) enhanced the LIGHT-mediated release of IL-8 in Huh7 hepatocytes. Hydrogen Peroxide 45-62 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 25749775-13 2015 Dexamethasone, calcitriol, anti-MD2/anti-TLR2 antibodies, and signalling inhibitors significantly reduced LPS+Der p2-induced IL-6/IL-8 secretion. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 26133108-8 2015 (iv) The reactive oxygen species (ROS) H2O2 (hydrogen peroxide) enhanced the LIGHT-mediated release of IL-8 in Huh7 hepatocytes. Hydrogen Peroxide 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 26133108-8 2015 (iv) The reactive oxygen species (ROS) H2O2 (hydrogen peroxide) enhanced the LIGHT-mediated release of IL-8 in Huh7 hepatocytes. Reactive Oxygen Species 9-32 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 26133108-8 2015 (iv) The reactive oxygen species (ROS) H2O2 (hydrogen peroxide) enhanced the LIGHT-mediated release of IL-8 in Huh7 hepatocytes. Reactive Oxygen Species 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 25626738-9 2015 Lower levels of MCP-1 and IL-8 (P < 0.001) and higher levels of IL-6 and MMP-9 (P = 0.003) were found in the sevoflurane group, compared with the TIVA group 30 min post-operatively. Sevoflurane 112-123 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 25749775-13 2015 Dexamethasone, calcitriol, anti-MD2/anti-TLR2 antibodies, and signalling inhibitors significantly reduced LPS+Der p2-induced IL-6/IL-8 secretion. Calcitriol 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 25934456-6 2015 Notably, this interaction between dimensionality and oxygen status via IL-8 increased angiogenic sprouting in a 3D endothelial invasion assay. Oxygen 53-59 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 25191838-10 2015 With regard to the mouthwash solutions, the lowest amounts of metal ions were released in CHX, and the highest amounts of metal ions were released in NaF + alcohol. Metals 122-127 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 25191838-10 2015 With regard to the mouthwash solutions, the lowest amounts of metal ions were released in CHX, and the highest amounts of metal ions were released in NaF + alcohol. Alcohols 156-163 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 25944880-10 2015 Palmitate, but not palmitoleate, elevated the expression of IL-6, IL-8, TLR2 (Toll-like receptor 2), and intercellular adhesion molecule 1 (ICAM-1). Palmitates 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 25930720-10 2015 After 8 weeks of pidotimod treatment, IL-8 was increased compared to either tiapride hydrochloride or haloperidol and pidotimod (P < 0.05). pidotimod 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 25929446-4 2015 Phloretin treatment decreased the production of IL-6, IL-8, CCL5, MDC, and TARC. Phloretin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 26018711-1 2015 Sodium 18F-fluoride (NaF) is a diagnostic marker for new bone formation in bone scintigraphy that was approved by US FDA in 1972 but discontinued in 1984. SODIUM FLUORIDE F-18 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 25458745-8 2015 IL-8 was significantly lower in Group HES than Group GEL at T1 (p=0.0005). Helium 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 26073057-8 2015 Furthermore, TRF from MGSO markedly reduced LPS-induced proinflammatory gene expression in human adipocytes and cytokine secretion to the medium (IL-6 and IL-8). mgso 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 25545021-6 2015 Inhibition of KCa3.1 by the selective, pore-blocking inhibitor TRAM-34, (and, in part, by siRNA) significantly reduced cell proliferation, as well as expression and secretion of pro-inflammatory factors (IL-6, IL-8, and MCP1) and the tissue-destructive protease MMP3. TRAM 34 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 26339358-5 2015 Honokiol inhibited the expression levels of IL-1beta, TNF-alpha, GM-CSF and IL-8 in PBMCs with a dose-dependent manner. honokiol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 26339358-7 2015 Furthermore, the mRNA and protein expression of IL-1beta, GM-CSF and IL-8 were up-regulated when the PBMCs exposure to TNF-alpha, however, honokiol treatment significantly reversed the expression of IL-1beta, TNF-alpha and GM-CSF in response to TNF-alpha with a dose-dependent manner. honokiol 139-147 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 26339358-8 2015 CONCLUSIONS: This study demonstrates that honokiol could possess potential anti-inflammatory effects and inhibits TNF-alpha-induced IL-1beta, GM-CSF and IL-8 production in PBMCs from rheumatoid arthritis patients. honokiol 42-50 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 26019243-11 2015 Moreover, GOSs stabilized the expression and cellular distribution of claudin3 and suppressed by >50% the deoxynivalenol-induced synthesis and release of interleukin-8 [IL8/chemokine CXC motif ligand (CXCL8)] (P < 0.05). deoxynivalenol 109-123 C-X-C motif chemokine ligand 8 Homo sapiens 157-170 25910974-4 2015 In this study poly(methyl methacrylate-divinylbenzene) (MMA-DVB) and poly(divinylbenzene) (DVB) were assessed with respect to their capacity to retain naphthalene (NAF) in continuous flow and batch processes (adsorption equilibrium and kinetics). poly(methyl methacrylate-divinylbenzene) 14-54 C-X-C motif chemokine ligand 8 Homo sapiens 164-167 25910974-4 2015 In this study poly(methyl methacrylate-divinylbenzene) (MMA-DVB) and poly(divinylbenzene) (DVB) were assessed with respect to their capacity to retain naphthalene (NAF) in continuous flow and batch processes (adsorption equilibrium and kinetics). poly(divinylbenzene) 69-89 C-X-C motif chemokine ligand 8 Homo sapiens 164-167 25952737-1 2015 UNLABELLED: Several studies have highlighted the role of vascular (18)F-NaF uptake as a marker of ongoing calcium deposition. Calcium 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 26019243-11 2015 Moreover, GOSs stabilized the expression and cellular distribution of claudin3 and suppressed by >50% the deoxynivalenol-induced synthesis and release of interleukin-8 [IL8/chemokine CXC motif ligand (CXCL8)] (P < 0.05). deoxynivalenol 109-123 C-X-C motif chemokine ligand 8 Homo sapiens 172-175 25952737-18 2015 CONCLUSION: Our results support the concept that (18)F-NaF is a feasible option in imaging molecular calcium deposition in the early stages of plaque formation, when active uptake mechanisms are the main determinants of calcium presence, but that retention of (18)F-NaF progressively decreases with increasing calcium deposition in the arterial wall. Calcium 101-108 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 26019243-11 2015 Moreover, GOSs stabilized the expression and cellular distribution of claudin3 and suppressed by >50% the deoxynivalenol-induced synthesis and release of interleukin-8 [IL8/chemokine CXC motif ligand (CXCL8)] (P < 0.05). deoxynivalenol 109-123 C-X-C motif chemokine ligand 8 Homo sapiens 204-209 25952737-18 2015 CONCLUSION: Our results support the concept that (18)F-NaF is a feasible option in imaging molecular calcium deposition in the early stages of plaque formation, when active uptake mechanisms are the main determinants of calcium presence, but that retention of (18)F-NaF progressively decreases with increasing calcium deposition in the arterial wall. Calcium 220-227 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 25952737-18 2015 CONCLUSION: Our results support the concept that (18)F-NaF is a feasible option in imaging molecular calcium deposition in the early stages of plaque formation, when active uptake mechanisms are the main determinants of calcium presence, but that retention of (18)F-NaF progressively decreases with increasing calcium deposition in the arterial wall. Calcium 220-227 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 26019243-12 2015 In mice, GOSs prevented the deoxynivalenol-induced mRNA overexpression of claudin3 (P = 0.022) and CXCL8 homolog keratinocyte hemoattractant (Kc) (Cxcl1) (P = 0.06) as well as the deoxynivalenol-induced morphologic defects. deoxynivalenol 28-42 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 25644373-0 2015 Recovery of urothelial mediator release but prolonged elevations in interleukin-8 and nitric oxide secretion following mitomycin C treatment. Mitomycin 119-130 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 26329674-8 2015 Serum IL-8 was highest in the SRDF group and reduced by IHVHF clearance. srdf 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 26329674-10 2015 Receiver operating characteristic curve analysis demonstrated that serum IL-8 predicted steroid sensitivity with moderate accuracy (area under the curve = 0.79, 95% CI: 0.69-0.87). Steroids 88-95 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 26329674-11 2015 IHVHF promotes remission in patients with steroid-resistant INS and it may be partly due to serum IL-8 clearance. Steroids 42-49 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 25882540-4 2015 Confirmatory enzyme-linked immunosorbent assays (ELISAs) showed that PGF2alpha stimulated increased output of interleukin (IL) 1beta, IL6, IL8 (CXCL8) and monocyte chemotactic protein-1 (MCP1, also known as chemokine (c-c motif) ligand 2, CCL2) by HUSMCs isolated from both upper and lower uterine segments. Dinoprost 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 25882540-4 2015 Confirmatory enzyme-linked immunosorbent assays (ELISAs) showed that PGF2alpha stimulated increased output of interleukin (IL) 1beta, IL6, IL8 (CXCL8) and monocyte chemotactic protein-1 (MCP1, also known as chemokine (c-c motif) ligand 2, CCL2) by HUSMCs isolated from both upper and lower uterine segments. Dinoprost 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 144-149 25882540-10 2015 Inhibition of ERK reversed PGF2alpha-induced IL1beta, IL6 and CCL2 output, while inhibition of PI3K blocked the effect of PGF2alpha on IL6, CXCL8 and CCL2 output and inhibition of NF-kappaB reversed PGF2alpha-induced IL1beta and CCL2 output. Dinoprost 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 140-145 25882540-10 2015 Inhibition of ERK reversed PGF2alpha-induced IL1beta, IL6 and CCL2 output, while inhibition of PI3K blocked the effect of PGF2alpha on IL6, CXCL8 and CCL2 output and inhibition of NF-kappaB reversed PGF2alpha-induced IL1beta and CCL2 output. Dinoprost 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 140-145 25881570-9 2015 Our results demonstrate that alantolactone from S. lappa suppresses TNF-alpha and IFN-gamma-induced production of RANTES and IL-8 by blocking STAT1 phosphorylation in HaCaT cells. alantolactone 29-42 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25644373-8 2015 A 326-fold increase in interleukin-8 secretion and significant increase in nitric oxide release were also detected at 24 h. One week after single and repeat MMC treatment, urothelial ATP, acetylcholine and PGE2 had recovered while the increase in nitric oxide and interleukin-8 was still evident. Mitomycin 157-160 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 25644373-8 2015 A 326-fold increase in interleukin-8 secretion and significant increase in nitric oxide release were also detected at 24 h. One week after single and repeat MMC treatment, urothelial ATP, acetylcholine and PGE2 had recovered while the increase in nitric oxide and interleukin-8 was still evident. Mitomycin 157-160 C-X-C motif chemokine ligand 8 Homo sapiens 264-277 26112052-10 2015 However, steroid treatment significantly decreased pro-inflammatory cytokines IL-1beta, IL-8, TNF and IFN-gamma at the time of organ procurement. Steroids 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 25746207-5 2015 The HIF-1alpha, AR, VEGF, and IL-8 were upregulated under 3% O2. Oxygen 61-63 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 26132391-4 2015 Exposure of ciPTEC to cationic uremic toxins initiated production of the inflammatory cytokines IL-6 (117 +- 3%, p < 0.001), IL-8 (122 +- 3%, p < 0.001), and ET-1 (134 +- 5%, p < 0.001). ciptec 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 26085988-9 2015 Inhibitors of Ca(2+)-dependent PKC (Ro-31-8220 and Go6976) significantly abolished hyphae-induced expression of IL-8. Go 6976 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 25904325-3 2015 Using HepG2 and primary human hepatocytes, we found that CHOP induces cell death and inflammatory responses after saturated free fatty acid exposure by activating NF-kappaB through a pathway involving IRAK2 expression, resulting in secretion of cytokines IL-8 and TNFalpha directly from hepatocytes. saturated free fatty acid 114-139 C-X-C motif chemokine ligand 8 Homo sapiens 255-259 25818949-0 2015 Hyaluronic acid decreases IL-6 and IL-8 secretion and permeability in an inflammatory model of interstitial cystitis. Hyaluronic Acid 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 26201230-1 2015 PURPOSE: To analyze whether immersion in sodium fluoride (NaF) solutions and/or common acidic beverages (test solutions) would affect the surface roughness or topography of lithium disilicate ceramic. Lithium 173-180 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 25751232-9 2015 Patients in the carbon dioxide group had lower concentrations of serum and BALF interleukin (IL)-1, IL-6, and IL-8, but higher serum concentrations of IL-10, accompanied by reduced numbers of cells and neutrophils as well as lower concentrations of protein in the BALF. Carbon Dioxide 16-30 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 26026083-4 2015 RESULTS: G1 arrest induced by SB265610 occurred at concentrations lacking CXCR2 selectivity, persisted upon interleukin 8 (IL8) challenge, and did not affect IL8 downstream target expression. 1-(2-bromophenyl)-3-(7-cyano-3H-benzotriazol-4-yl)urea 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 26026083-4 2015 RESULTS: G1 arrest induced by SB265610 occurred at concentrations lacking CXCR2 selectivity, persisted upon interleukin 8 (IL8) challenge, and did not affect IL8 downstream target expression. 1-(2-bromophenyl)-3-(7-cyano-3H-benzotriazol-4-yl)urea 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 25650123-10 2015 The IL-6 and IL-8 concentration was below the detection limit in all EBC samples. NSC638702 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 26026083-9 2015 CONCLUSION: The present study described the mechanisms for the anti-proliferative activity of SB265610 which may be of value in IL8-rich tumor microenvironments. 1-(2-bromophenyl)-3-(7-cyano-3H-benzotriazol-4-yl)urea 94-102 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 25619261-4 2015 In normal medium (0.4 mM calcium), citrate inhibited LPS-induced tumour necrosis factor (TNF)-alpha and interleukin (IL)-8 transcripts, whereas in medium supplemented with calcium (1.4 mM), TNF-alpha and IL-8 levels increased and appeared independent of calcium chelation. Citric Acid 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 104-122 25619261-4 2015 In normal medium (0.4 mM calcium), citrate inhibited LPS-induced tumour necrosis factor (TNF)-alpha and interleukin (IL)-8 transcripts, whereas in medium supplemented with calcium (1.4 mM), TNF-alpha and IL-8 levels increased and appeared independent of calcium chelation. Citric Acid 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 25619261-7 2015 In the presence of citrate, increased histone acetylation was observed in the TNF-alpha and IL-8 promoter regions of THP-1 cells. Citric Acid 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 25996641-4 2015 Phloretin inhibited levels of prostaglandin E2, decreased COX-2 expression, and suppressed IL-8, monocyte chemotactic protein 1, and IL-6 production. Phloretin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 25839901-5 2015 Treatment of THP-1 cells with extracts from 3R4F or pMRTP induced concentration-dependent increases in cytotoxicity (7-aminoactinomycin D), and inflammation (IL-8 and TNF-alpha). pmrtp 52-57 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 26473163-11 2015 RSV concentration significantly correlated with both IL-8 and RANTES at all-time points. Respiratory Syncytial Virus Vaccines 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 25803620-5 2015 Both intracellular and extracellular poly(I:C) induced the expression of IFNB, TNF, IL6, and IL8. Poly I-C 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 26082895-15 2015 CONCLUSION: Our exploratory correlative studies indicate that CEC and IL-8 changes may be predictive for response to O + C and prognostic in recurrent platinum-sensitive OvCa, requiring prospective validation. 2-n-octyl-4-isothiazolin-3-one 117-122 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 25840641-12 2015 Pretreatment with U0126 (ERK inhibitor) but not rapamycin (mTOR inhibitor) abrogated the IL-9-mediated IL-8 production. U 0126 18-23 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 26082895-15 2015 CONCLUSION: Our exploratory correlative studies indicate that CEC and IL-8 changes may be predictive for response to O + C and prognostic in recurrent platinum-sensitive OvCa, requiring prospective validation. Platinum 151-159 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 25975581-4 2015 The anti-inflammatory effect of isoacteoside was investigated in HMC-1 cells by studying the following markers: phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-induced interleukin (IL)-1beta, IL-6, IL-8, and tumor necrosis factor alpha (TNF-alpha) secretion and mRNA expression by ELISA and RT-PCR, respectively. isoacteoside 32-44 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 25975581-6 2015 Isoacteoside significantly suppressed the production and mRNA expression of proinflammatory cytokines including IL-1beta, IL-6, IL-8 and TNF-alpha in PMACI-stimulated HMC-1 cells without cytotoxicity. isoacteoside 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 25751776-5 2015 There were significant differences in gender, age, fever days, white blood cell count, C-reactive protein and blood glucose concentration and IL-8 levels among genotypes of IL-8-251A/T in EV71-infected patients, but no significant differences in alanine or aspartate aminotransferase, creatine kinase-myocardial isozyme and cerebrospinal fluid in patients with EV71 encephalitis. Glucose 116-123 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 25816245-4 2015 HNPs induce IL-8 in lung epithelial cells and monocytes through the P2Y6 signaling pathway. hnps 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 25816245-8 2015 The non-selective P2 receptor antagonists, suramin and pyridoxal phosphate-6-azo (benzene-2,4-disulfonic acid) tetrasodium salt hydrate (PPADS), significantly blocked the HNP-1-induced expression of IL-8 in the Caco-2 cells. Suramin 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 25816245-8 2015 The non-selective P2 receptor antagonists, suramin and pyridoxal phosphate-6-azo (benzene-2,4-disulfonic acid) tetrasodium salt hydrate (PPADS), significantly blocked the HNP-1-induced expression of IL-8 in the Caco-2 cells. pyridoxal phosphate-6-azo (benzene-2,4-disulfonic acid) tetrasodium salt hydrate 55-135 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 25816245-10 2015 In agreement with this finding, HNP-1 also significantly increased IL-8 production in the P2Y6-negative human colon cancer cell line, HT-29, and this increase was blocked by treatment with suramin and PPADS. Suramin 189-196 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 25816245-12 2015 However, the HNP-1-induced production of IL-8 was suppressed by the ERK1/2 inhibitor, U0126, but not by the p38 MAPK inhibitor, SB203580. U 0126 86-91 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 25910532-2 2015 The aim of this study was to determine whether the addition of ketamine reduces remifentanil-induced hyperalgesia; improves its analgesic effect; and alters interleukin 6 (IL-6), IL-8, and IL-10 levels. Ketamine 63-71 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 25840641-13 2015 Blockage of STIM1 with BTP2 or SKF96265 abrogated ERK phosphorylation and IL-8 production induced by IL-9. skf96265 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 25724683-7 2015 Ascorbic acid also enabled a greater suppression of IL8 secretion than when cells were treated with delta-Toc isoform alone. Ascorbic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 25715050-5 2015 rIFI16 caused dose/time-dependent upregulation of IL-6, IL-8, CCL2, CCL5, CCL20, ICAM1, VCAM1, and TLR4, while secretion of IL-6 and IL-8 was amplified with lipopolysaccharide synergy. rifi16 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 25715050-5 2015 rIFI16 caused dose/time-dependent upregulation of IL-6, IL-8, CCL2, CCL5, CCL20, ICAM1, VCAM1, and TLR4, while secretion of IL-6 and IL-8 was amplified with lipopolysaccharide synergy. rifi16 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 26043409-1 2015 Dental caries preventive agents, such as sodium fluoride (NaF) and bamboo salt (BS), are known to cause cellular growth that is characterized by morphological and gene expression changes. Sodium Fluoride 41-56 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 25556347-8 2015 Importantly, known suppressive effects of dexamethasone, a drug employed for the treatment of inflammatory bowel diseases, on leucocyte migration, IL8, IL6, and TNF-alpha production as well as CD86 surface expression by myeloid cells were observed in this model. Dexamethasone 42-55 C-X-C motif chemokine ligand 8 Homo sapiens 147-150 25651187-6 2015 Ethyl acetate extract decreased intracellular reactive oxygen species and significantly suppressed COX-2, IL-8, and prostaglandin E2 production and neutrophil chemotaxis by suppressing the translocation of the p65 subunit. ethyl acetate 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 25708117-10 2015 Intestinal epithelial cells represent a direct target of the action of olive oil phenols where they regulate IL-8 expression by transcriptional and posttranscriptional mechanisms. Phenols 81-88 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 25735562-4 2015 Thapsigargin stimulation of breast cancer cells induces IL8 expression in an NFAT-dependent manner. Thapsigargin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 25537341-6 2015 The concentration of interleukin-8 secreted from Calu-3 cells following stimulation with transforming growth factor-beta resulted in significantly lower level of interleukin-8 released from the cells pre-treated with clarithromycin (5.2 +- 0.5 ng.ml(-1) clarithromycin treated vs. 7.7 +- 0.8 ng.ml(-1) control, respectively). Clarithromycin 217-231 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 25537341-6 2015 The concentration of interleukin-8 secreted from Calu-3 cells following stimulation with transforming growth factor-beta resulted in significantly lower level of interleukin-8 released from the cells pre-treated with clarithromycin (5.2 +- 0.5 ng.ml(-1) clarithromycin treated vs. 7.7 +- 0.8 ng.ml(-1) control, respectively). Clarithromycin 217-231 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 25537341-6 2015 The concentration of interleukin-8 secreted from Calu-3 cells following stimulation with transforming growth factor-beta resulted in significantly lower level of interleukin-8 released from the cells pre-treated with clarithromycin (5.2 +- 0.5 ng.ml(-1) clarithromycin treated vs. 7.7 +- 0.8 ng.ml(-1) control, respectively). Clarithromycin 254-268 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 25537341-7 2015 CONCLUSIONS: Our data demonstrate that treatment with clarithromycin decreases the paracellular permeability of epithelial cells, mucus secretion and interleukin-8 release and therefore, inhaled clarithromycin holds potential as an anti-inflammatory therapy. Clarithromycin 54-68 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 25537341-7 2015 CONCLUSIONS: Our data demonstrate that treatment with clarithromycin decreases the paracellular permeability of epithelial cells, mucus secretion and interleukin-8 release and therefore, inhaled clarithromycin holds potential as an anti-inflammatory therapy. Clarithromycin 195-209 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 25950646-1 2015 The reaction of 1,2,4-triazole and NaF with M(ox) (M = transition-metal dication; ox = oxalate dianion) under hydrothermal conditions has led to the isolation of a variety of hybrid organic-inorganic coordination polymers. Metals 66-71 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 26521440-6 2015 Kaempferol significantly decreased the release of histamine, IL-6, IL-8, IL-1beta and TNF-alpha of activated HMC-1 mast cells (P<0.01). kaempferol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 26020773-7 2015 The production of IL-6, IL-8 and MMP-3 by chondrocytes significantly decreased in chitosan-alginate beads compared to alginate beads. Chitosan 82-90 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 26020773-7 2015 The production of IL-6, IL-8 and MMP-3 by chondrocytes significantly decreased in chitosan-alginate beads compared to alginate beads. Alginates 91-99 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 25985190-3 2015 In A549 lung epithelial cells in vitro we show that inhibition of basal PP2A activity by okadaic acid (OA) releases restraint on MAPKs and thereby increases MAPK-mediated pro-asthmatic cytokines, including IL-6 and IL-8. Okadaic Acid 89-101 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 25389358-10 2015 CpdA, similarly to prednisolone, down-regulated endogenous and TNF-alpha-induced IL-6, IL-8, MMP-1 and MMP-3 protein secretion. CPDA 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 25389358-11 2015 The dissociative effect of CpdA was confirmed using chondrocytes with no induction of leptin secretion, but with a significant decrease in IL-6, IL-8, MMP-1 and MMP-3 protein secretion. CPDA 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 25964092-8 2015 Furthermore, ACh stimulation increased the production of IL-8 and time-dependently induced the activation of EGFR, PI3K, and AKT through M3R. Acetylcholine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 25964092-11 2015 ACh-induced activation of EGFR/PI3K/AKT pathway and subsequent IL-8 upregulation may be one of the important mechanisms of M3R function. Acetylcholine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 25959257-7 2015 One component, 6-methyl-3,5-heptadien-2-one (MHDO), inhibited fMLF- and interleukin 8 (IL-8)-stimulated Ca(2+) flux, fMLF-induced chemotaxis, and PMA-induced ROS production in human neutrophils. 6-METHYL-3,5-HEPTADIEN-2-ONE 15-43 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 25959257-7 2015 One component, 6-methyl-3,5-heptadien-2-one (MHDO), inhibited fMLF- and interleukin 8 (IL-8)-stimulated Ca(2+) flux, fMLF-induced chemotaxis, and PMA-induced ROS production in human neutrophils. mhdo 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 25959257-7 2015 One component, 6-methyl-3,5-heptadien-2-one (MHDO), inhibited fMLF- and interleukin 8 (IL-8)-stimulated Ca(2+) flux, fMLF-induced chemotaxis, and PMA-induced ROS production in human neutrophils. Tetradecanoylphorbol Acetate 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 25959257-7 2015 One component, 6-methyl-3,5-heptadien-2-one (MHDO), inhibited fMLF- and interleukin 8 (IL-8)-stimulated Ca(2+) flux, fMLF-induced chemotaxis, and PMA-induced ROS production in human neutrophils. Reactive Oxygen Species 158-161 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 25950646-1 2015 The reaction of 1,2,4-triazole and NaF with M(ox) (M = transition-metal dication; ox = oxalate dianion) under hydrothermal conditions has led to the isolation of a variety of hybrid organic-inorganic coordination polymers. oxalate dianion 87-102 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 25950646-1 2015 The reaction of 1,2,4-triazole and NaF with M(ox) (M = transition-metal dication; ox = oxalate dianion) under hydrothermal conditions has led to the isolation of a variety of hybrid organic-inorganic coordination polymers. Polymers 213-221 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 25985190-3 2015 In A549 lung epithelial cells in vitro we show that inhibition of basal PP2A activity by okadaic acid (OA) releases restraint on MAPKs and thereby increases MAPK-mediated pro-asthmatic cytokines, including IL-6 and IL-8. Okadaic Acid 103-105 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 25725371-4 2015 Here, we demonstrate that human skin MCs display substantial susceptibility to RA by which they are instructed to increase pro-inflammatory mediators (IL-1beta, IL-8, TNF-alpha) but not histamine release. Tretinoin 79-81 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 25903726-3 2015 In unstimulated cells, ketamine also increased IL-8 production and mRNA expression. Ketamine 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 25961885-0 2015 In-vitro suppression of IL-6 and IL-8 release from human pulmonary epithelial cells by non-anticoagulant fraction of enoxaparin. Enoxaparin 117-127 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 25961885-3 2015 Our study indicated that enoxaparin inhibits the release of IL-6 and IL-8 from A549 pulmonary epithelial cells. Enoxaparin 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 25961885-13 2015 RESULTS: Enoxaparin (60 mug/mL) inhibited the release of IL-6 and IL-8 by >30%. Enoxaparin 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 25943109-11 2015 Additionally, LPS pre-incubation: 1) reduced dexamethasone"s capacity to inhibit FBS-induced IL-6, CXCL8 and RANTES, 2) reduced dexamethasone-induced GRalpha nuclear translocation (only in NM fibroblasts), 3) did not alter GRalpha/GRbeta expression, 4) decreased GILZ expression, and 5) did not affect dexamethasone"s capacity to induce MKP-1 and GILZ expression. Dexamethasone 45-58 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 25704613-10 2015 In EA.hy926 cells, DLC significantly inhibited the histamine- and LPS- induced IL-6 and IL-8 production and P-selectin and intercellular cell adhesion molecule-1 (ICAM-1) expression. Histamine 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 25943109-12 2015 MKP-1 knockdown reduced dexamethasone"s capacity to suppress FBS-induced CXCL8 release. Dexamethasone 24-37 C-X-C motif chemokine ligand 8 Homo sapiens 73-78 25746333-9 2015 We also found that lower viral replication after LiCl treatment was associated with the reduced mRNA levels of pro-inflammatory IL-8, IL-6, IL-1 beta, tumor necrosis factor alpha and decreased NF-kappaB nuclear translocation. Lithium Chloride 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 25713319-1 2015 Asthma is characterized by airway inflammation and remodeling and CXCL8 is a CXC chemokine that drives steroid-resistant neutrophilic airway inflammation. Steroids 103-110 C-X-C motif chemokine ligand 8 Homo sapiens 66-71 25591042-11 2015 Furthermore, the inhibitory effect of TGF-beta1 on 3"-5"-cyclic adenosine monophosphate-stimulated alveolar epithelial fluid transport required the presence of IL-8/cytokine-induced neutrophil chemoattractant-1 (n = 12 in each group). 3"-5"-cyclic adenosine monophosphate 51-87 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 25192219-10 2015 Supernatants from CS-treated neutrophils significantly increased the release of CXCL8 in normal human bronchial epithelial cells. Cesium 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 25296132-8 2015 When cAMP was increased, there was a concomitant increase in MKP-1 levels and significant inhibition of TNF-alpha-induced CXCL8 (IL-8). Cyclic AMP 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 25296132-8 2015 When cAMP was increased, there was a concomitant increase in MKP-1 levels and significant inhibition of TNF-alpha-induced CXCL8 (IL-8). Cyclic AMP 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 25791477-0 2015 Anticancer drug bortezomib increases interleukin-8 expression in human monocytes. Bortezomib 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 25791477-4 2015 Since monocytes and macrophages are major producers of IL-8, the goal of this study was to test the hypothesis that BZ increases the IL-8 expression in human monocytes and macrophages. Bortezomib 116-118 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 25791477-4 2015 Since monocytes and macrophages are major producers of IL-8, the goal of this study was to test the hypothesis that BZ increases the IL-8 expression in human monocytes and macrophages. Bortezomib 116-118 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 25791477-5 2015 Here, we show that BZ dramatically increases the IL-8 expression in lipopolysaccharide (LPS)-stimulated U937 macrophages as well as in unstimulated U937 monocytes and peripheral blood mononuclear cells, while it inhibits expression of IL-6, IL-1 and tumor necrosis factor-alpha. Bortezomib 19-21 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 25791477-6 2015 In addition, our results show that the underlying mechanisms involve p38 mitogen-activated protein kinase, which is required for the BZ-induced IL-8 expression. Bortezomib 133-135 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 25791477-7 2015 Together, these data suggest that the BZ-increased IL-8 expression in monocytes and macrophages may represent one of the mechanisms responsible for the BZ resistance and indicate that targeting the p38-mediated IL-8 expression could enhance the BZ effectiveness in cancer treatment. Bortezomib 38-40 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 25791477-7 2015 Together, these data suggest that the BZ-increased IL-8 expression in monocytes and macrophages may represent one of the mechanisms responsible for the BZ resistance and indicate that targeting the p38-mediated IL-8 expression could enhance the BZ effectiveness in cancer treatment. Bortezomib 38-40 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 25791477-7 2015 Together, these data suggest that the BZ-increased IL-8 expression in monocytes and macrophages may represent one of the mechanisms responsible for the BZ resistance and indicate that targeting the p38-mediated IL-8 expression could enhance the BZ effectiveness in cancer treatment. Bortezomib 152-154 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 25791477-7 2015 Together, these data suggest that the BZ-increased IL-8 expression in monocytes and macrophages may represent one of the mechanisms responsible for the BZ resistance and indicate that targeting the p38-mediated IL-8 expression could enhance the BZ effectiveness in cancer treatment. Bortezomib 152-154 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 25358442-7 2015 RESULTS: Dexamethasone reduced LPS-induced TNFalpha, IL-6 and CXCL-8 in all groups, but maximum inhibition was significantly reduced for GINA3/4 compared with GINA2 and GINA1 (P < 0.01). lps 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 62-68 25358442-7 2015 RESULTS: Dexamethasone reduced LPS-induced TNFalpha, IL-6 and CXCL-8 in all groups, but maximum inhibition was significantly reduced for GINA3/4 compared with GINA2 and GINA1 (P < 0.01). Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 62-68 26314120-5 2015 The existence of influencing substance (e. g. NaCl, NaF, Na2SO4, CaCl2 and turbidity) would inhibit the removal of Cr(VI) ions, and promote the removal of total Cr to some extent. Chromium 115-117 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 25813285-9 2015 Unfractionated heparin and LMWHs attenuated the TNF-alpha-mediated induction of CXCL8 and enhanced CXCL5, CCL2, and CCL5. Heparin 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 25640157-14 2015 In vitro, it modulated the IL-8 response to infection in a vitamin D concentration-dependent manner. Vitamin D 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 25813285-9 2015 Unfractionated heparin and LMWHs attenuated the TNF-alpha-mediated induction of CXCL8 and enhanced CXCL5, CCL2, and CCL5. Heparin, Low-Molecular-Weight 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 25813285-10 2015 The stimulating effect of thrombin on CXCL8 could be inhibited by heparin, whereas heparin had no impact on thrombin-induced CXCL1 and CCL2. Heparin 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 26314120-5 2015 The existence of influencing substance (e. g. NaCl, NaF, Na2SO4, CaCl2 and turbidity) would inhibit the removal of Cr(VI) ions, and promote the removal of total Cr to some extent. Chromium 161-163 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 25822013-12 2015 Furthermore, LF82 inhibited mucin gene expression (MUC2 and MUC5AC) in T84 cells while increasing the chemotactic IL-8 expression, both in a DPI-sensitive manner. diphenyleneiodonium 141-144 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 25748730-5 2015 Paeoniflorin reduced ConA-induced IL-8 mRNA expression and IL-8 release by 57.9% and 52.8%, respectively, and also decreased ConA-stimulated phosphorylation of ERK1/2 and Akt, suggesting paeoniflorin inhibits IL-8 expression and release by inhibiting the ERK1/2 and Akt pathways. peoniflorin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 25748730-0 2015 Paeoniflorin diminishes ConA-induced IL-8 production in primary human hepatic sinusoidal endothelial cells in the involvement of ERK1/2 and Akt phosphorylation. peoniflorin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 25748730-6 2015 Combining paeoniflorin with U0126 or LY294002 at low doses showed supra-additive inhibition of not only phospho-ERK1/2 and phospho-Akt by 46.4% and 35.0%, but also IL-8 release by 42.4% and 36.1% and IL-8 mRNA expression by 43.5% and 31.8%, respectively. peoniflorin 10-22 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 25748730-3 2015 We examined the effects and underlying mechanisms of paeoniflorin on IL-8 production in primary human hepatic sinusoidal endothelial cells (HHSECs). peoniflorin 53-65 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 25748730-5 2015 Paeoniflorin reduced ConA-induced IL-8 mRNA expression and IL-8 release by 57.9% and 52.8%, respectively, and also decreased ConA-stimulated phosphorylation of ERK1/2 and Akt, suggesting paeoniflorin inhibits IL-8 expression and release by inhibiting the ERK1/2 and Akt pathways. peoniflorin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 25748730-6 2015 Combining paeoniflorin with U0126 or LY294002 at low doses showed supra-additive inhibition of not only phospho-ERK1/2 and phospho-Akt by 46.4% and 35.0%, but also IL-8 release by 42.4% and 36.1% and IL-8 mRNA expression by 43.5% and 31.8%, respectively. peoniflorin 10-22 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 25748730-5 2015 Paeoniflorin reduced ConA-induced IL-8 mRNA expression and IL-8 release by 57.9% and 52.8%, respectively, and also decreased ConA-stimulated phosphorylation of ERK1/2 and Akt, suggesting paeoniflorin inhibits IL-8 expression and release by inhibiting the ERK1/2 and Akt pathways. peoniflorin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 25748730-6 2015 Combining paeoniflorin with U0126 or LY294002 at low doses showed supra-additive inhibition of not only phospho-ERK1/2 and phospho-Akt by 46.4% and 35.0%, but also IL-8 release by 42.4% and 36.1% and IL-8 mRNA expression by 43.5% and 31.8%, respectively. U 0126 28-33 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 25748730-6 2015 Combining paeoniflorin with U0126 or LY294002 at low doses showed supra-additive inhibition of not only phospho-ERK1/2 and phospho-Akt by 46.4% and 35.0%, but also IL-8 release by 42.4% and 36.1% and IL-8 mRNA expression by 43.5% and 31.8%, respectively. U 0126 28-33 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 26191223-6 2015 PE significantly inhibited poly (I:C)-induced expression of crucial psoriatic cytokines, such as IL-6, IL-8, CCL20 and TNF-alpha, via down-regulation of NF-kappaB signaling pathway in human keratinocytes. pe 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 25748730-6 2015 Combining paeoniflorin with U0126 or LY294002 at low doses showed supra-additive inhibition of not only phospho-ERK1/2 and phospho-Akt by 46.4% and 35.0%, but also IL-8 release by 42.4% and 36.1% and IL-8 mRNA expression by 43.5% and 31.8%, respectively. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 26191223-6 2015 PE significantly inhibited poly (I:C)-induced expression of crucial psoriatic cytokines, such as IL-6, IL-8, CCL20 and TNF-alpha, via down-regulation of NF-kappaB signaling pathway in human keratinocytes. Poly I-C 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 25748730-6 2015 Combining paeoniflorin with U0126 or LY294002 at low doses showed supra-additive inhibition of not only phospho-ERK1/2 and phospho-Akt by 46.4% and 35.0%, but also IL-8 release by 42.4% and 36.1% and IL-8 mRNA expression by 43.5% and 31.8%, respectively. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 25748730-7 2015 In conclusion, paeoniflorin most likely contributes to the therapy for liver disease by exerting anti-inflammatory effects on HHSECs through blocking IL-8 secretion via downregulation of ERK1/2 and Akt phosphorylation. peoniflorin 15-27 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 26505033-2 2015 Hollow silica microsphere-containing acrylate resin-based dental restoration materials were prepared by using hollow silica microspheres as NaF reservoirs. Silicon Dioxide 7-13 C-X-C motif chemokine ligand 8 Homo sapiens 140-143 25458910-0 2015 Randomized trial to evaluate azithromycin"s effects on serum and upper airway IL-8 levels and recurrent wheezing in infants with respiratory syncytial virus bronchiolitis. Azithromycin 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 25458910-3 2015 OBJECTIVES: We sought to investigate whether azithromycin treatment during RSV bronchiolitis reduces serum and nasal lavage IL-8 levels and the occurrence of postbronchiolitis recurrent wheezing. Azithromycin 45-57 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 25458910-7 2015 RESULTS: Compared with placebo, azithromycin treatment did not reduce serum IL-8 levels at day 8 (P = .6) but resulted in a greater decrease in nasal lavage fluid IL-8 levels by day 15 (P = .03). Azithromycin 32-44 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 25458910-10 2015 CONCLUSION: In this proof-of-concept study azithromycin treatment during RSV bronchiolitis reduced upper airway IL-8 levels, prolonged the time to the third wheezing episode, and reduced overall respiratory morbidity over the subsequent year. Azithromycin 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 25087735-7 2015 While free ODN and PSA-TMC nanoparticles coated with scrambled ODNs did not have substantial impacts on the inflammatory response, the decoy ODN-coated PSA-TMC nanoparticles were able to reduce the secretion of interleukin-6 and interleukin-8, pro-inflammatory mediators of CF, by the epithelial cells, particularly at longer time points. trimethylchlorosilane 156-159 C-X-C motif chemokine ligand 8 Homo sapiens 229-242 26505033-2 2015 Hollow silica microsphere-containing acrylate resin-based dental restoration materials were prepared by using hollow silica microspheres as NaF reservoirs. acrylate resin 37-51 C-X-C motif chemokine ligand 8 Homo sapiens 140-143 25736418-5 2015 AZD5069 was shown to inhibit binding of radiolabeled CXCL8 to human CXCR2 with a pIC50 value of 9.1. N-(2-(2,3-difluoro-6-benzylthio)-6-(3,4-dihydroxybutan-2-yloxy)pyrimidin-4-yl)azetidine-1-sulfonamide 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 53-58 25919031-9 2014 These changes were at least partly ensured by the increased concentration of MCP-1 and IL-8 at 5% O2. Oxygen 98-100 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 25987216-6 2015 In asthmatic children, we found that the serum levels of several polychlorinated biphenyl (PCB) congener sub-types were significantly positively correlated with interleukin (IL)-8 mRNA expression, whereas in a sub-group of children who displayed positive immunoglobulin E (IgE) responses to milk or egg proteins IL-22 mRNA expression was demonstrated to be useful for detecting the adverse health effects of environmental pollutants, particularly PCB congeners. Polychlorinated Biphenyls 65-89 C-X-C motif chemokine ligand 8 Homo sapiens 161-179 25987216-6 2015 In asthmatic children, we found that the serum levels of several polychlorinated biphenyl (PCB) congener sub-types were significantly positively correlated with interleukin (IL)-8 mRNA expression, whereas in a sub-group of children who displayed positive immunoglobulin E (IgE) responses to milk or egg proteins IL-22 mRNA expression was demonstrated to be useful for detecting the adverse health effects of environmental pollutants, particularly PCB congeners. Polychlorinated Biphenyls 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 161-179 25871388-5 2015 The effects of IL-8 on gefitinib-induced apoptosis, stemness, and in vivo tumorigenicity were investigated using established cell lines. Gefitinib 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 25871388-6 2015 We identified IL-8 was up-regulated in gefitinib-resistant cells, and high plasma IL-8 level was correlated with shorter progression-free-survival time. Gefitinib 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 25871388-7 2015 IL-8 overexpression suppressed gefitinib-induced apoptosis in gefitinib-sensitive cells. Gefitinib 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 25871388-7 2015 IL-8 overexpression suppressed gefitinib-induced apoptosis in gefitinib-sensitive cells. Gefitinib 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 25871388-8 2015 By contrast, suppression of IL-8 enhanced gefitinib-induced cell death in gefitinib-resistant cells. Gefitinib 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 25871388-8 2015 By contrast, suppression of IL-8 enhanced gefitinib-induced cell death in gefitinib-resistant cells. Gefitinib 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 25871388-10 2015 Consistently, knockdown of IL-8 leads to loss of stem cell-like characteristics in gefitinib-resistant cells. Gefitinib 83-92 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 25987216-7 2015 In conclusion, the mRNA expression levels of IL-8 and IL-22 can be used to detect children who are at particular risk of adverse health events caused by environmental pollutants, especially PCBs. Polychlorinated Biphenyls 190-194 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 25995631-0 2015 Oxidative stress by layered double hydroxide nanoparticles via an SFK-JNK and p38-NF-kappaB signaling pathway mediates induction of interleukin-6 and interleukin-8 in human lung epithelial cells. double 28-34 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 25995631-0 2015 Oxidative stress by layered double hydroxide nanoparticles via an SFK-JNK and p38-NF-kappaB signaling pathway mediates induction of interleukin-6 and interleukin-8 in human lung epithelial cells. hydroxide ion 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 25860871-9 2015 These findings suggest that PGG and PA may block or reduce the entry of the viruses into the cells to protect the cells from the virus destruction and abate virus replication, which may play an important role in interfering with expressions of rhinovirus receptors (intercellular adhesion molecule-1 and low-density lipoprotein receptor), inflammatory cytokines (interleukin (IL)-6, IL-8, tumor necrosis factor, interferon beta, and IL-1beta), and Toll-like receptor, which resulted in diminishing symptoms induced by HRV. pgg 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 383-387 25827911-1 2015 Utilizing a novel 8-silyloxyquinoline scaffold, we demonstrate the ability to synthesize fluorogenic probes for the sensitive and selective detection of inorganic fluoride (NaF) in aqueous samples. 8-silyloxyquinoline 18-37 C-X-C motif chemokine ligand 8 Homo sapiens 173-176 25827911-1 2015 Utilizing a novel 8-silyloxyquinoline scaffold, we demonstrate the ability to synthesize fluorogenic probes for the sensitive and selective detection of inorganic fluoride (NaF) in aqueous samples. inorganic fluoride 153-171 C-X-C motif chemokine ligand 8 Homo sapiens 173-176 25827911-4 2015 We demonstrate the ability to rationally tune the fluorescence and physical properties of the 8-silyloxyquinoline scaffold, producing a red-shifted fluoride probe (4) capable of detecting 50 muM (0.95 ppm) NaF in aqueous samples using a straightforward test-strip-based assay format. 8-silyloxyquinoline 94-113 C-X-C motif chemokine ligand 8 Homo sapiens 206-209 25827911-4 2015 We demonstrate the ability to rationally tune the fluorescence and physical properties of the 8-silyloxyquinoline scaffold, producing a red-shifted fluoride probe (4) capable of detecting 50 muM (0.95 ppm) NaF in aqueous samples using a straightforward test-strip-based assay format. Fluorides 148-156 C-X-C motif chemokine ligand 8 Homo sapiens 206-209 25767074-3 2015 Cucurbitacin B significantly inhibited imiquimod-induced expression of crucial psoriatic cytokines, such as IL-8 and CCL20, via down-regulation of NF-kappaB and STAT3 signaling pathway in human keratinocytes. cucurbitacin B 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 25767074-3 2015 Cucurbitacin B significantly inhibited imiquimod-induced expression of crucial psoriatic cytokines, such as IL-8 and CCL20, via down-regulation of NF-kappaB and STAT3 signaling pathway in human keratinocytes. Imiquimod 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 25915936-8 2015 RESULTS: Human rSSB stimulated IL-8 production from normal human neutrophils and HL-60 (RA) cells in a time- and dose-dependent manner. rssb 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 25915936-9 2015 This IL-8-stimulated activity was blocked by chloroquine and NH4Cl, indicating that endosomal acidification is important for this effect. Chloroquine 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 25915936-9 2015 This IL-8-stimulated activity was blocked by chloroquine and NH4Cl, indicating that endosomal acidification is important for this effect. Ammonium Chloride 61-66 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 25915936-10 2015 We found rSSB activated both MAPK pathway and nuclear factor-kappaB signaling to transcribe the IL-8 gene expression of cells. rssb 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 25915936-11 2015 Furthermore, tumor necrosis factor-alpha exerted an additive effect and rSSB-anti-SSB immune complex exhibited a synergistic effect on rSSB-induced IL-8 production. rssb 72-76 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 25637608-3 2015 We previously reported that the beta2-agonist fenoterol, direct activation of protein kinase A (PKA), and exchange factor directly activated by cAMP decrease cigarette smoke extract (CSE)-induced release of neutrophil attractant interleukin-8 (IL-8) from human airway smooth muscle (ASM) cells. Fenoterol 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 229-242 25637608-3 2015 We previously reported that the beta2-agonist fenoterol, direct activation of protein kinase A (PKA), and exchange factor directly activated by cAMP decrease cigarette smoke extract (CSE)-induced release of neutrophil attractant interleukin-8 (IL-8) from human airway smooth muscle (ASM) cells. Cyclic AMP 144-148 C-X-C motif chemokine ligand 8 Homo sapiens 229-242 25637608-3 2015 We previously reported that the beta2-agonist fenoterol, direct activation of protein kinase A (PKA), and exchange factor directly activated by cAMP decrease cigarette smoke extract (CSE)-induced release of neutrophil attractant interleukin-8 (IL-8) from human airway smooth muscle (ASM) cells. Cyclic AMP 144-148 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 25931819-7 2015 Additionally, this paper evidenced the dimer had the basic structural unit of Cu(2+)-FS in water, theoretically simulated the formation of Cu(2+)-FS nanoparticles, and identified that Cu(2+)-FS activity in decreasing glycoprotein IIb/IIIa, P-selectin, and IL-8 was responsible for the antithrombotic action. cu(2+)-fs 78-87 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 25931819-7 2015 Additionally, this paper evidenced the dimer had the basic structural unit of Cu(2+)-FS in water, theoretically simulated the formation of Cu(2+)-FS nanoparticles, and identified that Cu(2+)-FS activity in decreasing glycoprotein IIb/IIIa, P-selectin, and IL-8 was responsible for the antithrombotic action. Water 91-96 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 25931819-7 2015 Additionally, this paper evidenced the dimer had the basic structural unit of Cu(2+)-FS in water, theoretically simulated the formation of Cu(2+)-FS nanoparticles, and identified that Cu(2+)-FS activity in decreasing glycoprotein IIb/IIIa, P-selectin, and IL-8 was responsible for the antithrombotic action. cu(2+)-fs 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 25931819-7 2015 Additionally, this paper evidenced the dimer had the basic structural unit of Cu(2+)-FS in water, theoretically simulated the formation of Cu(2+)-FS nanoparticles, and identified that Cu(2+)-FS activity in decreasing glycoprotein IIb/IIIa, P-selectin, and IL-8 was responsible for the antithrombotic action. cu(2+)-fs 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 25926797-4 2015 We found that resveratrol reduced IL-6, IL-8, and MCP-1 levels in a concentration-dependent manner in adipocytes under inflammatory conditions. Resveratrol 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 25889494-5 2015 RESULTS: AICAR and metformin markedly reduced the IL-8 and GROalpha production induced by TNF-alpha. Metformin 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 25860871-9 2015 These findings suggest that PGG and PA may block or reduce the entry of the viruses into the cells to protect the cells from the virus destruction and abate virus replication, which may play an important role in interfering with expressions of rhinovirus receptors (intercellular adhesion molecule-1 and low-density lipoprotein receptor), inflammatory cytokines (interleukin (IL)-6, IL-8, tumor necrosis factor, interferon beta, and IL-1beta), and Toll-like receptor, which resulted in diminishing symptoms induced by HRV. paeonol 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 383-387 25856395-5 2015 Curcumin pre-treatment also abrogated the gp120-mediated upregulation of the proinflammatory cytokines tumor necrosis factor-alpha and interleukin (IL)-6, which mediate barrier disruption, as well as the chemokines IL-8, RANTES and interferon gamma-induced protein-10 (IP-10), which are capable of recruiting HIV target cells to the FGT. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 25937780-9 2015 Higher mRNA and supernate secretion levels of IL-1beta, IL-6 and IL-8 were detected in SPC-A1 after being cocultured with TAMs. tams 122-126 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 25683465-12 2015 Furthermore, in epithelial cells from resection material of patients with Crohn"s disease and ulcerative colitis, high expression of CXCL-8 was associated with a reduced choline acetyl transferase expression, suggesting an aberrant epithelial production of ACh in inflammatory context. Acetylcholine 257-260 C-X-C motif chemokine ligand 8 Homo sapiens 133-139 25646974-5 2015 When combining all four study groups, statistically significant positive correlations included uPCR with urine IL-8, urine MCP-1, urine IP-10, and serum IP-10 and uACR with urine IL-8, urine B2M, serum IP-10, and serum B2M. uacr 163-167 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 25608533-9 2015 EPS-stimulated mRNA expression levels of MYH7, IL-6, and IL-8 correlated negatively with subjects" HbA1c and/or fasting plasma glucose, suggesting an effect linked to the diabetic phenotype. eps 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 25608533-9 2015 EPS-stimulated mRNA expression levels of MYH7, IL-6, and IL-8 correlated negatively with subjects" HbA1c and/or fasting plasma glucose, suggesting an effect linked to the diabetic phenotype. Glucose 127-134 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 25394884-5 2015 RESULTS: Increasing concentrations of glucose significantly increased trophoblast secretion of the inflammatory cytokines/chemokines: IL-1beta, IL-6, IL-8, GRO-alpha, RANTES, and G-CSF; significantly increased trophoblast secretion of the anti-angiogenic factors sFlt-1 and sEndoglin; and significantly decreased trophoblast migration. Glucose 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 25937780-13 2015 CONCLUSIONS: These findings demonstrated that TAMs may enhance IL-1beta, IL-6 and IL-8 expressions via TLRs signaling pathway. tams 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 25515776-9 2015 The production of IL6 and IL8 was also suppressed by p38 inhibitor SB203580. SB 203580 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 25575297-6 2015 A selective Ca(2+) chelator, BAPTA-AM, prevented TRP channel agonists-mediated IL-6 and IL-8 induction. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 25515776-6 2015 Poly(dA:dT) induced the expression of pro-inflammatory cytokine genes including IFN-beta, TNF-alpha, IL-6 and IL-8 as well, whereas the pro-inflammatory cytokine production was suppressed by RIG-I siRNA, but not by AIM2 siRNA. poly 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 25690135-16 2015 ACN extract and M3G significantly attenuated TNF-alpha-stimulated low-grade leukocyte adhesion, expression of adhesion molecules E-selectin, VCAM-1 and ICAM-1 and cytokine expression and secretion (IL-8 and IL-6) as well as NF-kappaB mRNA expression. Anthocyanins 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 25515776-6 2015 Poly(dA:dT) induced the expression of pro-inflammatory cytokine genes including IFN-beta, TNF-alpha, IL-6 and IL-8 as well, whereas the pro-inflammatory cytokine production was suppressed by RIG-I siRNA, but not by AIM2 siRNA. amsonic acid 5-7 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 25515776-6 2015 Poly(dA:dT) induced the expression of pro-inflammatory cytokine genes including IFN-beta, TNF-alpha, IL-6 and IL-8 as well, whereas the pro-inflammatory cytokine production was suppressed by RIG-I siRNA, but not by AIM2 siRNA. Thymidine 8-10 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 25611805-5 2015 Phlorizin also decreased the expression of UVB-induced pro-inflammatory cytokines, such as interleukin-1 beta (IL-1beta), interleukin-6 (IL-6) and interleukin-8 (IL-8) at the mRNA level. Phlorhizin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 25611805-5 2015 Phlorizin also decreased the expression of UVB-induced pro-inflammatory cytokines, such as interleukin-1 beta (IL-1beta), interleukin-6 (IL-6) and interleukin-8 (IL-8) at the mRNA level. Phlorhizin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 25708600-6 2015 RESULTS: Niclosamide reduced the secretion of IL-1beta, IL-6, IL-8, IL-17A and IFN-gamma from TNF-alpha-induced RA FLS in a dose-dependent manner. Niclosamide 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 25532794-8 2015 Poly(I:C) induced activation of TLR-2 contributes to stronger cell responses to a TLR-2 agonist and regulation of these synergistic responses may take place at the mRNA level of IL-6 and IL-8. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 25519802-8 2015 DHMEQ significantly suppressed the production of both IL-8 and MCP-1 in IL-1beta-stimulated HCFs. dehydroxymethylepoxyquinomicin 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 25519802-11 2015 CONCLUSIONS: The suppression of inflammatory chemokines IL-8 and MCP-1 and inhibition of the expression of ICAM-1 in cultured HCFs by DHMEQ indicates that DHMEQ may have a therapeutic potential for treating ICAM-1 and chemokine-mediated corneal inflammatory disorders. dehydroxymethylepoxyquinomicin 155-160 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 25625672-1 2015 OBJECTIVES: To evaluate the anti-erosive potential of solutions containing sodium fluoride (NaF, 225 ppm F) and different film-forming agents. Sodium Fluoride 75-90 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 25659498-11 2015 AMPK activators AICAR, phenformin and A769662 significantly decreased IL-6 and IL-8 stimulated by LPS, flagellin and poly(I:C). Phenformin 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 25872712-2 2015 Although both oxidative and endoplasmic reticulum (ER) stresses have been implicated in fluorosis, the signaling pathways and their roles in sodium fluoride (NaF)-induced apoptosis of Sertoli cells have been sparsely described. Sodium Fluoride 141-156 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 25872712-6 2015 In addition, NaF exposure facilitated the accumulation of ROS and increased nuclear translocation of nuclear factor erythroid 2-related factor 2 (Nrf2) in Sertoli cells. Reactive Oxygen Species 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 25872712-7 2015 Treatment with NAC caused remarkable recovery from these NaF-induced responses. Acetylcysteine 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 25872712-9 2015 NAC effectively blocked the activation of ER stress, suggesting that NaF-induced ROS is an early event that triggers ER stress. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 25872712-9 2015 NAC effectively blocked the activation of ER stress, suggesting that NaF-induced ROS is an early event that triggers ER stress. Reactive Oxygen Species 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 25872712-10 2015 Taken together, the results demonstrate that the ROS-mediated ER stress pathway is the crucial mechanistic event involved in NaF-induced apoptosis of Sertoli cells. Reactive Oxygen Species 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 25675966-3 2015 The release of interleukin-8 (IL-8) from human epidermal keratinocytes stimulated by the addition of 100 mug ml(-1) beta-glucan of Saccharomyces cerevisiae was significantly inhibited by LCZ at the concentration of 10(-5) mol l(-1). latoconazole 187-190 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 25675966-3 2015 The release of interleukin-8 (IL-8) from human epidermal keratinocytes stimulated by the addition of 100 mug ml(-1) beta-glucan of Saccharomyces cerevisiae was significantly inhibited by LCZ at the concentration of 10(-5) mol l(-1). latoconazole 187-190 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 24854880-11 2015 Interestingly, small interfering RNA (siRNA) knock down of the TLR2 and ERK1/2 inhibitor, PD98059, abolished the effects of P. gingivalis LPS on the bone sialoprotein mRNA level, whereas siRNA knock down of the TLR2 and p38 MAPK inhibitor, SB203580, blocked the effect of P. gingivalis LPS on IL-8 in hPDLFs. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 90-97 C-X-C motif chemokine ligand 8 Homo sapiens 293-297 25604035-7 2015 RESULTS: PF4:heparin complexes caused release of the biomarker interleukin 8 in whole blood, and the level of response varied with the stoichiometric ratio of PF4 to heparin. Heparin 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 25604035-7 2015 RESULTS: PF4:heparin complexes caused release of the biomarker interleukin 8 in whole blood, and the level of response varied with the stoichiometric ratio of PF4 to heparin. Heparin 166-173 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 25595138-8 2015 Improvements in ACQ and/or AQLQ scores with atorvastatin and ICS were associated with decreases in G-CSF, IL-7, CCL2 and CXCL8. acenaphthenequinone 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 121-126 25595138-8 2015 Improvements in ACQ and/or AQLQ scores with atorvastatin and ICS were associated with decreases in G-CSF, IL-7, CCL2 and CXCL8. aqlq 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 121-126 25595138-8 2015 Improvements in ACQ and/or AQLQ scores with atorvastatin and ICS were associated with decreases in G-CSF, IL-7, CCL2 and CXCL8. Atorvastatin 44-56 C-X-C motif chemokine ligand 8 Homo sapiens 121-126 25870718-3 2015 Control discs were removed before subjects rinsed with 0.1% chlorhexidine digluconate (CHX) or 0.2% sodium fluoride (NaF) for 1 minute. Sodium Fluoride 100-115 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 25756398-10 2015 CONCLUSIONS: Interleukin-8, sVEGFR-3, and SDF-1alpha were identified as predictors of sunitinib clinical outcome. Sunitinib 86-95 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 25695485-0 2015 IL8 polymorphisms and overall survival in pazopanib- or sunitinib-treated patients with renal cell carcinoma. pazopanib 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 25695485-0 2015 IL8 polymorphisms and overall survival in pazopanib- or sunitinib-treated patients with renal cell carcinoma. Sunitinib 56-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 25695485-4 2015 RESULTS: In study 1, four SNPs showed nominally significant association (P<=0.05) with OS; two of these SNPs (rs1126647, rs4073) in IL8 were associated (P<=0.05) with OS in study 2. Osmium 90-92 C-X-C motif chemokine ligand 8 Homo sapiens 135-138 25695485-7 2015 CONCLUSIONS: Variant alleles of IL8 polymorphisms are associated with poorer survival outcomes in pazopanib- or sunitinib-treated patients with aRCC. pazopanib 98-107 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 25695485-7 2015 CONCLUSIONS: Variant alleles of IL8 polymorphisms are associated with poorer survival outcomes in pazopanib- or sunitinib-treated patients with aRCC. Sunitinib 112-121 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 25451977-5 2015 Both in human myometrium and amnion, OT-induced activation of the canonical NF-kappaB pathway upregulated key inflammatory labour-associated genes including IL-8, CCL5, IL-6 and COX-2. Oxytocin 37-39 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 25695485-7 2015 CONCLUSIONS: Variant alleles of IL8 polymorphisms are associated with poorer survival outcomes in pazopanib- or sunitinib-treated patients with aRCC. arcc 144-148 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 25660662-4 2015 The results show that production of IL-1beta, IL-6 and IL-8 was significantly higher in the group of methadone-maintained patients than in the healthy control group. Methadone 101-110 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 25657098-3 2015 The experimental results prove that the NaF : Ln(3+) molar ratio influences significantly the growth process of the nanocrystals, i.e. a low NaF : Ln(3+) molar ratio results in hexagonal NaScF4 nanocrystals, while a high NaF : Ln(3+) molar ratio favors monoclinic Na3ScF6 nanocrystals. nascf4 187-193 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 25657098-3 2015 The experimental results prove that the NaF : Ln(3+) molar ratio influences significantly the growth process of the nanocrystals, i.e. a low NaF : Ln(3+) molar ratio results in hexagonal NaScF4 nanocrystals, while a high NaF : Ln(3+) molar ratio favors monoclinic Na3ScF6 nanocrystals. nascf4 187-193 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 25657098-3 2015 The experimental results prove that the NaF : Ln(3+) molar ratio influences significantly the growth process of the nanocrystals, i.e. a low NaF : Ln(3+) molar ratio results in hexagonal NaScF4 nanocrystals, while a high NaF : Ln(3+) molar ratio favors monoclinic Na3ScF6 nanocrystals. nascf4 187-193 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 25657098-3 2015 The experimental results prove that the NaF : Ln(3+) molar ratio influences significantly the growth process of the nanocrystals, i.e. a low NaF : Ln(3+) molar ratio results in hexagonal NaScF4 nanocrystals, while a high NaF : Ln(3+) molar ratio favors monoclinic Na3ScF6 nanocrystals. na3scf6 264-271 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 25657098-3 2015 The experimental results prove that the NaF : Ln(3+) molar ratio influences significantly the growth process of the nanocrystals, i.e. a low NaF : Ln(3+) molar ratio results in hexagonal NaScF4 nanocrystals, while a high NaF : Ln(3+) molar ratio favors monoclinic Na3ScF6 nanocrystals. na3scf6 264-271 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 25657098-3 2015 The experimental results prove that the NaF : Ln(3+) molar ratio influences significantly the growth process of the nanocrystals, i.e. a low NaF : Ln(3+) molar ratio results in hexagonal NaScF4 nanocrystals, while a high NaF : Ln(3+) molar ratio favors monoclinic Na3ScF6 nanocrystals. na3scf6 264-271 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 25888119-10 2015 In a univariate analysis IL6 and IL8 levels were associated with SAA>6.4 mg/l (OR=1.74 and 1.46; 95% CI=1.00-3.03 and 1.06-2.01; p=0.051 and 0.02 respectively) and hsCRP>3 mg/l in (OR=2.00 and 1.37; 95% CI=1.09-3.69 and 1.02-1.85; p=0.026 and 0.039 respectively). hscrp 167-172 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 25660271-1 2015 We report the design and synthesis of an aquacarbonyl Ru(II) dication cis-[Ru(CO)2(H2O)4](2+) reagent for histidine (His)-selective metallation of interleukin (IL)-8 at site 33. ru(ii) 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 147-165 25660271-1 2015 We report the design and synthesis of an aquacarbonyl Ru(II) dication cis-[Ru(CO)2(H2O)4](2+) reagent for histidine (His)-selective metallation of interleukin (IL)-8 at site 33. cis-[ru(co)2(h2o)4](2+) reagent 70-101 C-X-C motif chemokine ligand 8 Homo sapiens 147-165 25660271-1 2015 We report the design and synthesis of an aquacarbonyl Ru(II) dication cis-[Ru(CO)2(H2O)4](2+) reagent for histidine (His)-selective metallation of interleukin (IL)-8 at site 33. Histidine 106-115 C-X-C motif chemokine ligand 8 Homo sapiens 147-165 25660271-1 2015 We report the design and synthesis of an aquacarbonyl Ru(II) dication cis-[Ru(CO)2(H2O)4](2+) reagent for histidine (His)-selective metallation of interleukin (IL)-8 at site 33. Histidine 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 147-165 25646691-0 2015 Gemcitabine-induced CXCL8 expression counteracts its actions by inducing tumor neovascularization. gemcitabine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 20-25 25646691-4 2015 We observed that gemcitabine enhanced selectively the expression of CXCL8 in human pancreatic cancer cells through ROS generation and NF-kappaB activation. gemcitabine 17-28 C-X-C motif chemokine ligand 8 Homo sapiens 68-73 25646691-4 2015 We observed that gemcitabine enhanced selectively the expression of CXCL8 in human pancreatic cancer cells through ROS generation and NF-kappaB activation. Reactive Oxygen Species 115-118 C-X-C motif chemokine ligand 8 Homo sapiens 68-73 25646691-6 2015 Gemcitabine also enhanced CXCL8 expression in pancreatic cancer cells in xenografted tumor tissues. gemcitabine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 25646691-7 2015 Moreover, anti-CXCL8 antibody treatment in vivo attenuated tumor formation as well as intra-tumoral vascularity in nude mice, which were transplanted with Miapaca-2 cells and treated with gemcitabine. gemcitabine 188-199 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 25646691-8 2015 Thus, gemcitabine-induced CXCL8 may counteract the drug through inducing neovascularization. gemcitabine 6-17 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 25595472-5 2015 The studied Ti-Bi alloys showed better corrosion resistance than pure Ti in both AS (artificial saliva) and ASFL (AS containing 0.2% NaF and 0.3% lactic acid) solutions. Titanium 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 133-136 25002707-2 2015 Most recent studies on glucose stabilities confirm that the sodium fluoride/potassium oxalate (NaF/KOx) tube is far from the gold standard. Glucose 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 25002707-2 2015 Most recent studies on glucose stabilities confirm that the sodium fluoride/potassium oxalate (NaF/KOx) tube is far from the gold standard. Sodium Fluoride 60-75 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 25002707-2 2015 Most recent studies on glucose stabilities confirm that the sodium fluoride/potassium oxalate (NaF/KOx) tube is far from the gold standard. Oxalic Acid 76-93 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 25002707-4 2015 Greiner has introduced a glucose-specific tube (Glucomedics) containing NaF/KOx, citrate, and EDTA to minimise glycolysis. Glucose 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 26016020-2 2015 An increase in the IL-6, IL-8, TNF-alpha and p53 genes expression in the concentration range of silver and titanium dioxide nanoparticles of 10-40 muk g/ml was found. Silver 96-102 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 26016020-2 2015 An increase in the IL-6, IL-8, TNF-alpha and p53 genes expression in the concentration range of silver and titanium dioxide nanoparticles of 10-40 muk g/ml was found. titanium dioxide 107-123 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 24806810-5 2015 RESULTS: P. gingivalis LPS induced cytokine/chemokine (IL-6, IL-8, MCP-1, and GRO) protein production in HGFs, and this effect was suppressed by azithromycin at all concentrations tested. Azithromycin 145-157 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 25403159-4 2015 Sesaminol also inhibited the expression of IL-8 and IL-6 mRNA following CSE exposure. sesaminol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 25769104-6 2015 ADE extracts induced Nrf2 activity and IL-8 mRNA levels significantly more than Non-ADE. Adenine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 24106166-4 2015 At a concentration of 0.1 muM, Pb(2+) induced IL-8 gene activation in gastric carcinoma AGS cells. Lead 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 24106166-6 2015 Upregulation of the IL-8 gene was abrogated by the MEK inhibitor, PD98059, and partially suppressed by the epidermal growth factor receptor inhibitors, AG1478 and PD153035. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 24106166-6 2015 Upregulation of the IL-8 gene was abrogated by the MEK inhibitor, PD98059, and partially suppressed by the epidermal growth factor receptor inhibitors, AG1478 and PD153035. RTKI cpd 152-158 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 24106166-6 2015 Upregulation of the IL-8 gene was abrogated by the MEK inhibitor, PD98059, and partially suppressed by the epidermal growth factor receptor inhibitors, AG1478 and PD153035. 4-((3-bromophenyl)amino)-6,7-dimethoxyquinazoline 163-171 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 24106166-7 2015 Furthermore, c-Jun protein expression was induced in cells treated with Pb(2+) , and overexpression of c-Jun enhanced Pb(2+) -induced IL-8 activation. Lead 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 25454806-0 2015 Unfractionated heparin attenuates LPS-induced IL-8 secretion via PI3K/Akt/NF-kappaB signaling pathway in human endothelial cells. Heparin 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 24106166-7 2015 Furthermore, c-Jun protein expression was induced in cells treated with Pb(2+) , and overexpression of c-Jun enhanced Pb(2+) -induced IL-8 activation. Lead 118-120 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 25454806-4 2015 Pretreatment with UFH (0.1-1U/ml) significantly inhibited LPS (10mug/ml)-stimulated interleukin (IL)-6 and IL-8 production in HPMECs. Heparin 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 25454806-6 2015 Inhibition studies by using wortmannin abrogated NF-kappaB-mediated IL-6 and IL-8 expression, suggesting the requirement of PI3K/Akt pathway. Wortmannin 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 25590211-0 2015 Metformin reverts the secretion of CXCL8 induced by TNF-alpha in primary cultures of human thyroid cells: an additional indirect anti-tumor effect of the drug. Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 24766418-7 2015 Additionally, glutamine suppressed the production and mRNA expression of inflammatory cytokines including interleukin-1beta (IL-1beta), TNF-alpha, and IL-8. Glutamine 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 24786562-13 2015 Changes in normalized IL-6 and IL-8 levels upon treatment with L-mimosine did not reach the level of significance (P > 0.05), whilst treatment with IL-1, which served as positive control, increased IL-6 (P < 0.05) and IL-8 levels (P < 0.05). Mimosine 63-73 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 25808165-10 2015 However, most of the metals including (V(+4), V(+5)), (Cr(+3), Cr(+6)), Zn, and Pb inhibited the production of both IL-6 and IL-8. Chromium 55-57 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25808165-10 2015 However, most of the metals including (V(+4), V(+5)), (Cr(+3), Cr(+6)), Zn, and Pb inhibited the production of both IL-6 and IL-8. Chromium 63-65 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25808165-10 2015 However, most of the metals including (V(+4), V(+5)), (Cr(+3), Cr(+6)), Zn, and Pb inhibited the production of both IL-6 and IL-8. Zinc 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25808165-10 2015 However, most of the metals including (V(+4), V(+5)), (Cr(+3), Cr(+6)), Zn, and Pb inhibited the production of both IL-6 and IL-8. Lead 80-82 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25590211-4 2015 OBJECTIVE: This study aimed to evaluate whether metformin inhibits the secretion of CXCL8 induced by Tumor-Necrosis-Factor-alpha (TNF-alpha) in primary cultures of normal and tumor human thyroid cells as well as in thyroid cancer cell lines. Metformin 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 84-89 25590211-7 2015 RESULTS: Metformin significantly and dose-dependently inhibited the TNF-alpha-induced CXCL8 secretion in both normal thyrocytes (ANOVA: F = 42.04; P < .0001) and papillary thyroid cancer cells (ANOVA: F = 21.691; P < .0001) but not in TPC-1 and BCPAP cell lines. Metformin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 86-91 25590211-8 2015 CONCLUSION: Metformin inhibits the TNF-alpha-induced CXCL8 secretion in primary cultures of normal thyroid cells and differentiated thyroid cancer cells at least of the most frequent poorly aggressive phenotype. Metformin 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 53-58 25590211-10 2015 Thus, the here-reported inhibiting effect of metformin on TNF-alpha-induced CXCL8 secretion could be considered as a further indirect anticancer property of the drug. Metformin 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 76-81 25467970-0 2015 Epoxyeicosatrienoic acids attenuate cigarette smoke extract-induced interleukin-8 production in bronchial epithelial cells. epoxyeicosatrienoic acids 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 25538104-8 2015 Fexofenadine significantly inhibited the upregulated expression of IL-8 in HCT116 and COLO205 cells stimulated with TNF-alpha. fexofenadine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 25481370-0 2015 Lipoteichoic acid from Lactobacillus plantarum inhibits Pam2CSK4-induced IL-8 production in human intestinal epithelial cells. lipoteichoic acid 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 25554564-0 2015 The atypical antipsychotic clozapine selectively inhibits interleukin 8 (IL-8)-induced neutrophil chemotaxis. Clozapine 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 25554564-0 2015 The atypical antipsychotic clozapine selectively inhibits interleukin 8 (IL-8)-induced neutrophil chemotaxis. Clozapine 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 25554564-3 2015 We found that clozapine, within the therapeutic concentration range, potently and selectively inhibits PMN chemotaxis induced by interleukin 8 (IL-8), a chemokine inducing neutrophil migration. Clozapine 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 129-142 25554564-3 2015 We found that clozapine, within the therapeutic concentration range, potently and selectively inhibits PMN chemotaxis induced by interleukin 8 (IL-8), a chemokine inducing neutrophil migration. Clozapine 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 25554564-3 2015 We found that clozapine, within the therapeutic concentration range, potently and selectively inhibits PMN chemotaxis induced by interleukin 8 (IL-8), a chemokine inducing neutrophil migration. platensimycin 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 129-142 25554564-3 2015 We found that clozapine, within the therapeutic concentration range, potently and selectively inhibits PMN chemotaxis induced by interleukin 8 (IL-8), a chemokine inducing neutrophil migration. platensimycin 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 25554564-7 2015 An interference of clozapine with the autocrine release of leukotriene B4 (LTB4), a secondary chemoattractant secreted by neutrophils in response to the primary chemoattractant IL-8, was hypothesized. Clozapine 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 25554564-7 2015 An interference of clozapine with the autocrine release of leukotriene B4 (LTB4), a secondary chemoattractant secreted by neutrophils in response to the primary chemoattractant IL-8, was hypothesized. Leukotriene B4 59-73 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 25554564-8 2015 In agreement with this hypothesis, clozapine attenuated the IL-8-induced release of LTB4 in PMNs. Clozapine 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 25554564-10 2015 Intriguingly MK-571, an inhibitor of the multi-drug resistance protein MRP4, playing a pivotal role in effluxing LTB4, completely blocked PMN chemotaxis induced by IL-8, but gave conflicting results when tested for its ability to reduce LTB4 release, increasing LTB4 efflux by itself but reducing the release when in combination with IL-8. verlukast 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 25554564-10 2015 Intriguingly MK-571, an inhibitor of the multi-drug resistance protein MRP4, playing a pivotal role in effluxing LTB4, completely blocked PMN chemotaxis induced by IL-8, but gave conflicting results when tested for its ability to reduce LTB4 release, increasing LTB4 efflux by itself but reducing the release when in combination with IL-8. verlukast 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 334-338 25467970-4 2015 Treatment with 11,12-EET or 14,15-EET attenuated the CSE-induced release of interleukin (IL)-8 by inhibiting the phosphorylation of p38 mitogen-activated protein kinases (MAPKs). 11,12-epoxy-5,8,14-eicosatrienoic acid 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 76-94 25467970-4 2015 Treatment with 11,12-EET or 14,15-EET attenuated the CSE-induced release of interleukin (IL)-8 by inhibiting the phosphorylation of p38 mitogen-activated protein kinases (MAPKs). 14,15-epoxy-5,8,11-eicosatrienoic acid 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 76-94 25458486-6 2015 Our results showed that both Na3Au (S2O3)2 2H2O and HgCl2 induce substantial release of IL-8, but not IL-6, CCL2 or IL-10, from MoDc, PBMC, or THP-1 cells. na3au (s2o3)2 2h2o 29-47 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 25458486-6 2015 Our results showed that both Na3Au (S2O3)2 2H2O and HgCl2 induce substantial release of IL-8, but not IL-6, CCL2 or IL-10, from MoDc, PBMC, or THP-1 cells. Mercuric Chloride 52-57 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 25433332-8 2015 CB126 decreased the abundance of Interleukin-8 both at the mRNA and protein levels. cb126 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 25723478-10 2015 H1R and H2R, but not H3R or H4R, were constitutively expressed by primary and immortalized cells, and epithelial histamine stimulation induced GM-CSF, TNFalpha, and IL-8, but not TSLP or eotaxin-3 secretion. Histamine 113-122 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 25656974-7 2015 The expression of IL-8 and TNF-alpha was negatively correlated with l-lactate and positively correlated with NH3 and putrescine, whereas the expression of IFN-gamma was positively correlated with histamine and 4-ethylphenol (P< 0 05). L-lactate 68-77 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 25656974-7 2015 The expression of IL-8 and TNF-alpha was negatively correlated with l-lactate and positively correlated with NH3 and putrescine, whereas the expression of IFN-gamma was positively correlated with histamine and 4-ethylphenol (P< 0 05). Ammonia 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 25656974-7 2015 The expression of IL-8 and TNF-alpha was negatively correlated with l-lactate and positively correlated with NH3 and putrescine, whereas the expression of IFN-gamma was positively correlated with histamine and 4-ethylphenol (P< 0 05). Putrescine 117-127 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 25898559-8 2015 RESULTS: DP-M&O decreased the levels of TNF-alpha, IL-1beta, IL-6, and IL-8 and increased that of IL-10 in a concentration-dependent manner. 3-(3,5-dichlorophenyl)-1-methyl-2,5-pyrrolidinedione 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 25898559-8 2015 RESULTS: DP-M&O decreased the levels of TNF-alpha, IL-1beta, IL-6, and IL-8 and increased that of IL-10 in a concentration-dependent manner. Adenosine Monophosphate 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 25723478-11 2015 Epithelial priming with the TLR3 ligand poly (I:C) induced H1R and H2R expression, and enhanced histamine-induced GM-CSF, TNFalpha, and IL-8 secretion. Histamine 96-105 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 25689147-8 2015 Receiver-operator characteristic curves showed that IL-8 predicted the relative change in plasma creatinine less than 10% (area under curve (AUC), 0.80; P = 0.0007). Creatinine 97-107 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 25821694-9 2015 At a distinct concentration (100 microg/mL) aSNP-plain displayed the highest cytotoxicity and IL-8 release in monocultures of A549. asnp 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 25689147-9 2015 Multivariate analyses showed that lower IL-8 transcripts, longer time on dialysis, higher recipient body mass index and deceased donor type were associated with relative change in plasma creatinine at the first postoperative day less than 10%. Creatinine 187-197 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 25689147-3 2015 We investigated whether transcript levels in mononuclear cells including IL-8 on the first postoperative day may be involved in immediate allograft dysfunction as defined by reduced relative change in plasma creatinine at the first postoperative day. Creatinine 208-218 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 25556927-2 2015 In this paper, aluminum-free Mn-beta zeolite was hydrothermally synthesized in the SiO2-MnO2-(TEA)2O-NaF-H2O system. Aluminum 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 25689147-7 2015 RESULTS: Transcript levels of IL-8 and S100A8 were significantly lower in patients with relative change in plasma creatinine less than 10% at the first postoperative day. Creatinine 114-124 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 25659107-4 2015 Using a three-dimensional collagen assay chemokinetic and chemotactic migration induced by CXCL8 was inhibited with the pan PI3 Kinase inhibitor wortmannin. Wortmannin 145-155 C-X-C motif chemokine ligand 8 Homo sapiens 91-96 25659107-5 2015 Analysis of the specific Class I PI3 Kinase catalytic isoforms alpha, delta and gamma using the inhibitors PIK-75, PIK-294 and AS-605240 respectively indicated differential roles in CXCL8-induced neutrophil migration. 5-quinoxalin-6-ylmethylenethiazolidine-2,4-dione 127-136 C-X-C motif chemokine ligand 8 Homo sapiens 182-187 25659107-7 2015 AS-605240 markedly reduced CXCL8 induced chemokinetic migration but had no effect on CXCL8 induced chemotactic migration. 5-quinoxalin-6-ylmethylenethiazolidine-2,4-dione 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 27-32 25821678-8 2015 The PLLA-Fe particle showed a significant increase in the IL-8 release in hMSCs but not in hHSCs. Iron 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 25849726-6 2015 RESULTS: Non-responders patients treated with macrolide containing regimens showed significantly lower levels of IL-6 and TNF-alpha in bronchoalveolar lavage fluid and lower IL-8 and IL-10 in blood than those patients treated with non-macrolide regimens. Macrolides 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 25652132-8 2015 The TLR3 agonist poly I:C 10 mug/mL increased the IL-8 release in HBECs that was poorly inhibited by dexamethasone in smokers (24.5%) and smokers with COPD (21.6%). Poly I-C 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 25556927-2 2015 In this paper, aluminum-free Mn-beta zeolite was hydrothermally synthesized in the SiO2-MnO2-(TEA)2O-NaF-H2O system. sio2-mno2-(tea)2o 83-100 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 25658801-5 2015 Durum wheat extracts significantly inhibited the secretion of the pro-inflammatory IL-8 mediator at 66 microg/mL of phenolic acids and at 0.2 microg/mL of isoprenoids. phenolic acid 116-130 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 25658801-5 2015 Durum wheat extracts significantly inhibited the secretion of the pro-inflammatory IL-8 mediator at 66 microg/mL of phenolic acids and at 0.2 microg/mL of isoprenoids. Terpenes 155-166 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 25556927-2 2015 In this paper, aluminum-free Mn-beta zeolite was hydrothermally synthesized in the SiO2-MnO2-(TEA)2O-NaF-H2O system. Water 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 25678784-7 2015 Inhibition of LPS-induced CXCL8 release by dexamethasone (10(-6) M) was reduced, and baseline and LPS-induced p38 MAPK activation increased in PBMCs of COPD. Dexamethasone 43-56 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 25172696-0 2015 Anti-inflammatory effect of chlorogenic acid on the IL-8 production in Caco-2 cells and the dextran sulphate sodium-induced colitis symptoms in C57BL/6 mice. Chlorogenic Acid 28-44 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 25678784-8 2015 GW856553 (10(-9) and 10(-10) M) synergistically increased the inhibitory effect of dexamethasone (10(-8) and 10(-6) M) on LPS-induced CXCL8 release in COPD. 6-(5-((cyclopropylamino)carbonyl)-3-fluoro-2-methylphenyl)-N-(2,2-dimethylprpyl)-3-pyridinecarboxamide 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 134-139 25678784-8 2015 GW856553 (10(-9) and 10(-10) M) synergistically increased the inhibitory effect of dexamethasone (10(-8) and 10(-6) M) on LPS-induced CXCL8 release in COPD. Dexamethasone 83-96 C-X-C motif chemokine ligand 8 Homo sapiens 134-139 25601738-9 2015 CONCLUSIONS: These findings suggest, for the first time, a potential effect of benzene exposure on ALA-D activity, CD80 and CD86 expression, IL-8 levels, which could be suggested as potential markers for the early detection of benzene-induced alterations. Benzene 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 25661379-7 2015 Consistently, the combined exposure of romidepsin and bortezomib reversed the effects on IkappaB degradation as evident with IL-8, p50 and p65 (NF-kappaB) expression. Bortezomib 54-64 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25172696-2 2015 Effects of CHA and CHA metabolites were evaluated on the IL-8 production in human intestinal Caco-2 cells induced by combined stimulation with tumour necrosis factor alpha (TNFalpha) and H2O2. Chlorogenic Acid 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 25172696-2 2015 Effects of CHA and CHA metabolites were evaluated on the IL-8 production in human intestinal Caco-2 cells induced by combined stimulation with tumour necrosis factor alpha (TNFalpha) and H2O2. Chlorogenic Acid 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 25536369-5 2015 While the steroid dexamethasone brought about a 41.6% reduction in the IL-8 concentration in the supernatant, the 5kDaR reduced IL-8 by 59% (P < 0.05) when compared to the TNFalpha stimulated Caco-2 cells. Steroids 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 25536369-5 2015 While the steroid dexamethasone brought about a 41.6% reduction in the IL-8 concentration in the supernatant, the 5kDaR reduced IL-8 by 59% (P < 0.05) when compared to the TNFalpha stimulated Caco-2 cells. Dexamethasone 18-31 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 25172696-2 2015 Effects of CHA and CHA metabolites were evaluated on the IL-8 production in human intestinal Caco-2 cells induced by combined stimulation with tumour necrosis factor alpha (TNFalpha) and H2O2. Hydrogen Peroxide 187-191 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 25172696-3 2015 CHA and caffeic acid (CA) inhibited TNFalpha- and H2O2-induced IL-8 production. Chlorogenic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 25172696-3 2015 CHA and caffeic acid (CA) inhibited TNFalpha- and H2O2-induced IL-8 production. caffeic acid 8-20 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 25172696-3 2015 CHA and caffeic acid (CA) inhibited TNFalpha- and H2O2-induced IL-8 production. Hydrogen Peroxide 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 25561369-5 2015 RESULTS: Adrenaline(A), noradrenaline and the beta-AR agonist isoprenaline reduced N-formyl-Met-Leu-Phe (fMLP)-induced migration, CD11b/CD18 expression, and ROS production, without affecting IL-8. Epinephrine 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 25398834-8 2015 Gene expression signature, induced by lenalidomide in nurse-like cells, indicated a reduction of pivotal pro-survival signals for chronic lymphocytic leukemia, such as CCL2, IGF1, CXCL12, HGF1, and supported a modulation towards M1 phenotype with high IL2 and low IL10, IL8 and CD163. Lenalidomide 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 270-273 25398638-7 2015 beta-Carotene significantly reduced IL8 (1,306.2-253.75 pg/ml), decreased light and heavy ferritin by 77.8 and 45.8%, respectively, and increased ferroportin by 59.9% (P < 0.05). beta Carotene 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 25398638-8 2015 Increasing iron concentrations and incubation periods resulted in increased IL8 release. Iron 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 25398638-11 2015 beta-Carotene normalized the main iron-related proteins" levels, reduced IL8 production, and released intracellular trapped iron. beta Carotene 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 25528475-8 2015 Our results revealed that T11TS therapy induced downregulation of TNF-alpha, IL-8, IL-6, and NF-kappaB confirmed by FACS assay and ELISA. t11ts 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 25561369-5 2015 RESULTS: Adrenaline(A), noradrenaline and the beta-AR agonist isoprenaline reduced N-formyl-Met-Leu-Phe (fMLP)-induced migration, CD11b/CD18 expression, and ROS production, without affecting IL-8. Norepinephrine 24-37 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 25561369-5 2015 RESULTS: Adrenaline(A), noradrenaline and the beta-AR agonist isoprenaline reduced N-formyl-Met-Leu-Phe (fMLP)-induced migration, CD11b/CD18 expression, and ROS production, without affecting IL-8. Isoproterenol 62-74 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 24559390-10 2015 In human bronchial epithelial cells, ZnONP-induced interleukin-8 secretion was partially prevented by co-treatment with the Toll-like receptor 4 (TLR4) inhibitor. znonp 37-42 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 23835780-10 2015 Our results show that alendronate inhibits keratinocyte viability, expression of IL-8, VEGF, and collagen type I which are intimately related to healing events and cell migration while promoting apoptosis. Alendronate 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 25256809-8 2015 T-cell receptor (TCR) activation of PBMCs and nickel (Ni(2+) ) treatments of human dermal microvascular endothelial cells (HDMECs) were performed resulting in IL-4, IL-6, IL-8 and IL-17 production. Nickel 46-52 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 25256809-8 2015 T-cell receptor (TCR) activation of PBMCs and nickel (Ni(2+) ) treatments of human dermal microvascular endothelial cells (HDMECs) were performed resulting in IL-4, IL-6, IL-8 and IL-17 production. Nickel(2+) 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 25256809-11 2015 Similarly, TSC inhibits overproduction of IL-4 and IL-17 in T-cell receptor (TCR)-activated PBMCs as well as nickel induction of IL-6 and IL-8 in HDMECs. Nickel 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 25453468-0 2015 The effect of the decoy molecule PA401 on CXCL8 levels in bronchoalveolar lavage fluid of patients with cystic fibrosis. pa401 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 42-47 25453468-2 2015 Glycosaminoglycans (GAGs) possess the ability to influence the chemokine profile of the CF lung by binding CXCL8 and protecting it from proteolytic degradation. Glycosaminoglycans 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 107-112 25453468-3 2015 CXCL8 is maintained in an active state by this glycan interaction thus increasing infiltration of immune cells such as neutrophils into the lungs. Polysaccharides 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 25453468-4 2015 As the CXCL8-based decoy PA401 displays no chemotactic activity, yet demonstrates glycan binding affinity, the aim of this study was to investigate the anti-inflammatory effect of PA401 on CXCL8 levels, and activity, in CF airway samples in vitro. pa401 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 7-12 25453468-4 2015 As the CXCL8-based decoy PA401 displays no chemotactic activity, yet demonstrates glycan binding affinity, the aim of this study was to investigate the anti-inflammatory effect of PA401 on CXCL8 levels, and activity, in CF airway samples in vitro. pa401 180-185 C-X-C motif chemokine ligand 8 Homo sapiens 189-194 25453468-6 2015 CXCL8 in CF BALF pre and post exposure to PA401 was quantified by ELISA. pa401 42-47 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 25453468-9 2015 RESULTS: Exposure of CF BALF to increasing concentrations of PA401 (50-1000pg/ml) over a time course of 2-12h in vitro, significantly reduced the level of detectable CXCL8 (P<0.05). pa401 61-66 C-X-C motif chemokine ligand 8 Homo sapiens 166-171 25453468-10 2015 Interestingly, PA401 engendered release of CXCL8 from GAGs exposing the chemokine susceptible to proteolysis. pa401 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 25453468-13 2015 CONCLUSION: PA401 can disrupt CXCL8:GAG complexes, rendering the chemokine susceptible to proteolytic degradation. pa401 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 30-35 25592441-6 2015 The aim of this paper is to evaluate the role of (18)F-NaF sodium fluoride ((18)F-NaF) positron emission tomography (PET) in distinguishing between septic and aseptic failure in hip and knee replacements, in addition to evaluating the feasibility of using multi-sequential (18)F-NaF PET-CT for the assessment of painful lower limb prostheses. Sodium Fluoride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 25453468-13 2015 CONCLUSION: PA401 can disrupt CXCL8:GAG complexes, rendering the chemokine susceptible to proteolytic degradation. Glycosaminoglycans 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 30-35 25453468-14 2015 Clinical application of a CXCL8 decoy, such as PA401, may serve to decrease the inflammatory burden in the CF lung in vivo. pa401 47-52 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 25351664-6 2015 Moreover, the ability of 2PS to reduce H2 O2 -induced IL-8 secretion, a marker of inflammation and oxidative stress, was abrogated in Nrf2 knockdown cells. Hydrogen Peroxide 39-44 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 25273157-7 2015 Treatment with levosimendan strongly attenuated IL-1beta-induced expression of IL-6 and IL-8 in HACM as well as E-selectin and ICAM-1 in ECs. Simendan 15-27 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 25592441-6 2015 The aim of this paper is to evaluate the role of (18)F-NaF sodium fluoride ((18)F-NaF) positron emission tomography (PET) in distinguishing between septic and aseptic failure in hip and knee replacements, in addition to evaluating the feasibility of using multi-sequential (18)F-NaF PET-CT for the assessment of painful lower limb prostheses. Sodium Fluoride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 25592441-6 2015 The aim of this paper is to evaluate the role of (18)F-NaF sodium fluoride ((18)F-NaF) positron emission tomography (PET) in distinguishing between septic and aseptic failure in hip and knee replacements, in addition to evaluating the feasibility of using multi-sequential (18)F-NaF PET-CT for the assessment of painful lower limb prostheses. Sodium Fluoride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 25593029-0 2015 Involvement of intracellular calcium mobilization in IL-8 activation in human retinal pigment epithelial cells. Calcium 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 25424854-11 2015 A greater increase in posttreatment urinary IL8 during the 6-week period was observed in patients receiving MMC + BCG compared with patients receiving BCG monotherapy. Mitomycin 108-111 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 25973337-1 2015 Fluorine 18 Sodium Fluoride ((18)F-NaF) (sodium fluoride) PET/CT is a highly sensitive but is a non-specific method for identifying bone metastases. Fluorine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 25973337-1 2015 Fluorine 18 Sodium Fluoride ((18)F-NaF) (sodium fluoride) PET/CT is a highly sensitive but is a non-specific method for identifying bone metastases. Sodium Fluoride 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 25973337-1 2015 Fluorine 18 Sodium Fluoride ((18)F-NaF) (sodium fluoride) PET/CT is a highly sensitive but is a non-specific method for identifying bone metastases. Sodium Fluoride 41-56 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 25593029-3 2015 The purpose of this study is to understand the molecular mechanisms by which calcium signaling controls IL-8 activation in human RPE cells. Calcium 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 25593029-7 2015 RESULTS: Our study reported that intracellular calcium mobilization activated IL-8 gene expression and secretion. Calcium 47-54 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 25785032-0 2015 Ghrelin inhibits AngII -induced expression of TNF-alpha, IL-8, MCP-1 in human umbilical vein endothelial cells. Ghrelin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 25593029-8 2015 Application of pharmacological inhibitor BAY 11-7082, siRNA, and plasmids of the nuclear factor kappa light chain enhancer of activated B cells (NF-kappaB) binding site, we identified that NF-kappaB is the main transcription factor involved in intracellular calcium mobilization-mediated IL-8 activation in human RPE cells. Calcium 258-265 C-X-C motif chemokine ligand 8 Homo sapiens 288-292 25785032-5 2015 The aim of this study is to examine the effect of ghrelin on angiotension II (AngII)-induced expression of TNF-alpha, MCP-1, IL-8 in HUVECs. Ghrelin 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25593029-9 2015 CONCLUSIONS: Collectively, our findings highlight the important role of intracellular calcium mobilization in the activation of IL-8. Calcium 86-93 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 25785032-10 2015 RESULT: our study showed that ghrelin inhibited AngII -induced expression of IL-8, TNF-alpha and MCP-1 in the HUVECs via GHSR pathway in concentration- and time-dependent manners. Ghrelin 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 25757924-7 2015 In contrast, GJBRH significantly reduced the production of MDC, RANTES, and IL-8 compared with control cells simulated with TNF-alpha and IFN-gamma. gjbrh 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 25559824-11 2015 Finally, PMA + ionomycin stimulation did not induce significant alterations on MSCs phenotype but did increase indoleamine-2,3-dioxygenase (IDO), inducible costimulatory ligand (ICOSL), IL-1beta, IL-8, and TNF-alpha mRNA expression. Tetradecanoylphorbol Acetate 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 25559824-11 2015 Finally, PMA + ionomycin stimulation did not induce significant alterations on MSCs phenotype but did increase indoleamine-2,3-dioxygenase (IDO), inducible costimulatory ligand (ICOSL), IL-1beta, IL-8, and TNF-alpha mRNA expression. Ionomycin 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 24285492-8 2015 RESULTS: In rheumatoid arthritis synovial fibroblasts (RASF), FFA dose-dependently enhanced the secretion of the proinflammatory cytokine IL-6, the chemokines IL-8 and MCP-1, as well as the matrix-degrading enzymes pro-MMP1 and MMP3. Fatty Acids, Nonesterified 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 26327186-4 2015 Stability of emixustat in blood collected with and without anticoagulant (NaF/KOx) on the VAMS device at ambient, refrigerated and frozen conditions was established. vams 90-94 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 25445541-4 2015 The LPS-induced release of these cytokines was also modulated by purinergic receptor activation since IL-8 and MCP-1 release was decreased by the nucleotide scavenger apyrase as well as by the pharmacological P2Y6 receptor antagonists suramin and MRS2578. Suramin 235-242 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 25445541-4 2015 The LPS-induced release of these cytokines was also modulated by purinergic receptor activation since IL-8 and MCP-1 release was decreased by the nucleotide scavenger apyrase as well as by the pharmacological P2Y6 receptor antagonists suramin and MRS2578. N,N''-1,4-butanediylbis(N'-(3-isothiocyanatophenyl))thiourea 247-254 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 25757924-8 2015 Consistently, GJBRH suppressed the mRNA expression of MDC, RANTES, and IL-8 in TNF-alpha and IFN-gamma-treated cells. gjbrh 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 26339601-4 2015 In the present study, global expression profiling of short noncoding RNAs, in particular miRNAs and snoRNAs, was carried out in sodium fluoride (NaF) treated human osteosarcoma (HOS) cells to understand their possible role in the development of fluorosis. Sodium Fluoride 128-143 C-X-C motif chemokine ligand 8 Homo sapiens 145-148 26339601-8 2015 We show that the alterations in UG dinucleotides and D-box sequences of snoRNAs could be due to NaF exposure. Dinucleoside Phosphates 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 26090385-6 2015 Cytokine expression analysis in media of sepiolite NC treated cultures showed a proinflammatory profile (INFgamma, IL-1alpha, IL-8, and IL-6), in contrast with clinoptilolite NC that induced lees cytokines with concomitant production of IL-10. magnesium trisilicate 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 26491668-4 2015 Additionally, the expression of cyclooxygenase-2 (COX-2) and interleukin-8 (IL-8) mRNA was significantly reduced by the combination treatment as compared to the expression seen for treatment with cetuximab or cisplatin alone. Cisplatin 209-218 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 26491668-4 2015 Additionally, the expression of cyclooxygenase-2 (COX-2) and interleukin-8 (IL-8) mRNA was significantly reduced by the combination treatment as compared to the expression seen for treatment with cetuximab or cisplatin alone. Cisplatin 209-218 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 26491668-6 2015 Results demonstrate that combined treatment with cetuximab and cisplatin exerts synergistic anticancer effects on colon cancer cells and also suggest that the ERK pathway plays a critical role in these effects via the suppression of the EGFR signaling pathway, along with the inhibition of COX-2, IL-8, and AP-1 and NF-kappaB. Cisplatin 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 297-301 25451615-0 2015 Increased cerebrospinal fluid interleukin-8 in bipolar disorder patients associated with lithium and antipsychotic treatment. Lithium 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 26510263-6 2015 After 24 hours, compared to the isoflurane group, the propofol group had significantly lower levels of CRP (P < 0.001), IL-6 (P < 0.001) and IL-8 (P < 0.001), with higher levels CD11 (P = 0.009) and CD18 (P = 0.002) expression. Propofol 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 25451615-8 2015 IL-8 concentrations were positively associated to lithium- and antipsychotic treatment. Lithium 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24882386-7 2015 In TNF-alpha-treated neutrophils, pre-incubation with everolimus provided the most potent effect, simultaneously reducing the release of both VEGF and IL-8 while doubling the release of IL-1RA. Everolimus 54-64 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 26121010-5 2015 The effect of leptin on IL-8 could visibly abolished by the inhibitor of PI3K LY294002. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 78-86 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 24882386-6 2015 Under basal conditions, mammalian target of rapamycin (mTOR) inhibitors (sirolimus and everolimus) had the most potent anti-inflammatory effect, decreasing both IL-8 release ( -80%) and vascular endothelial growth factor (VEGF) release ( -65%) and preserving the release of the anti-inflammatory cytokine interleukin-1 receptor antagonist (IL-1RA). Sirolimus 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 25139172-4 2015 In general terms, non-flavonoid polyphenols reduce the production of inflammatory mediators, such as IL-1beta, IL-8, MCP-1, COX-2 or iNOS in these animal models of diabetes. Polyphenols 32-43 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 24882386-6 2015 Under basal conditions, mammalian target of rapamycin (mTOR) inhibitors (sirolimus and everolimus) had the most potent anti-inflammatory effect, decreasing both IL-8 release ( -80%) and vascular endothelial growth factor (VEGF) release ( -65%) and preserving the release of the anti-inflammatory cytokine interleukin-1 receptor antagonist (IL-1RA). Everolimus 87-97 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 25344634-7 2015 The serum concentrations of several sub-types of polychlorinated biphenyl (PCB) congeners were found to be significantly correlated with interleukin (IL)-8 mRNA expression among asthmatic children. Polychlorinated Biphenyls 49-73 C-X-C motif chemokine ligand 8 Homo sapiens 137-155 26238371-6 2015 IL-1beta, IL-6, IL-8 and TNF-alpha production could be significantly upregulated and downregulated by a ROS activator or inhibitor, respectively. Reactive Oxygen Species 104-107 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 26728736-2 2015 Ethanol-induced ulceration causes an increased transcription of IFNa, IL-8, and IL-12 mRNA in BMNCs. Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 26728736-4 2015 The sizes of acetate-induced damages were positively correlated with the expression of IL-10 and IL-8 genes in BMNCs and with the expression of IFNa, IL-2, IL-12, and TNF genes in GM cells. Acetates 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 26728736-5 2015 Intranasal administration of Pro-Gly-Pro (PGP) reduced ethanol-induced ulceration, activating the transcription of IFNgamma, IL-2, and IL-4 mRNA in BMNCs and prevents the formation of stress- and acetateinduced ulcers by inhibiting the expression of IL-8 and IL-10 genes, respectively. prolyl-glycyl-proline 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 26728736-5 2015 Intranasal administration of Pro-Gly-Pro (PGP) reduced ethanol-induced ulceration, activating the transcription of IFNgamma, IL-2, and IL-4 mRNA in BMNCs and prevents the formation of stress- and acetateinduced ulcers by inhibiting the expression of IL-8 and IL-10 genes, respectively. prolyl-glycyl-proline 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 25344634-7 2015 The serum concentrations of several sub-types of polychlorinated biphenyl (PCB) congeners were found to be significantly correlated with interleukin (IL)-8 mRNA expression among asthmatic children. Polychlorinated Biphenyls 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 137-155 25344634-10 2015 In conclusion, IL-8 and IL-22 mRNA expressions could be useful biomarkers for detecting sub-populations of children who are particularly vulnerable to the adverse health effects of environmental pollutants, especially PCBs. Polychlorinated Biphenyls 218-222 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 25972907-9 2015 Within the PG2 signature, there were five genes associated with doxorubicin: IL-8, MDM4, BCL2, PRODH2, and BIRC5. Doxorubicin 64-75 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 26495958-6 2015 In H292 cells, fully-sulfated HMW heparin significantly reduced LPS-induced gene expression of both COX-2 and CXCL-8 for up to 48 hours, while desulfated heparin had little to no significant suppressive effect on signaling or on COX-2 gene or protein expression. Heparin 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 110-116 25055998-7 2015 We also found that poly-IC-induced mRNA expression of other proinflammatory mediators such as MCP-1, RANTES, and IL-8 was suppressed by licochalcone A. Poly I-C 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 25055998-7 2015 We also found that poly-IC-induced mRNA expression of other proinflammatory mediators such as MCP-1, RANTES, and IL-8 was suppressed by licochalcone A. licochalcone 136-148 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 26495958-8 2015 In contrast, in normal HBE-1 cells, fully sulfated heparin significantly suppressed only ERK signaling, COX-2 gene expression at 12 hours, and CXCL-8 gene expression at 6 and 12 hours, while desulfated heparin had no significant effects on LPS-stimulated signaling or on gene or protein expression. Heparin 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 143-149 25838833-7 2015 BHSST significantly suppressed the production of RANTES/CCL5, TARC/CCL17, MDC/CCL22, and IL-8 in TI-stimulated HaCaT cells. bhsst 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 26495958-7 2015 Desulfated heparin, initially ineffective at preventing LPS-induced CXCL8 up-regulation, reduced CXCL8 transcription at 24 hours. Heparin 11-18 C-X-C motif chemokine ligand 8 Homo sapiens 97-102 26121924-5 2015 Peiminine inhibits the production of the pro-inflammatory cytokine, such as interleukin (IL)-6, IL-8, tumor necrosis factor-alpha (TNF-alpha) and IL-1beta (IL-1beta). peiminine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 26436853-0 2015 Short-Chain Fatty Acids Regulate Secretion of IL-8 from Human Intestinal Epithelial Cell Lines in vitro. Fatty Acids, Volatile 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 25312962-6 2015 NaHS treatment reduced both spontaneous and IL-1beta-induced secretion of IL-6, IL-8 and RANTES in different experimental settings. sodium bisulfide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 25817163-5 2015 At 40 and/or 100 mug/ml, mtDAMPs activated human neutrophils, indicated by a significant reduction in the surface expression of L-selectin, and triggered a number of functional responses from both resting and tumour necrosis factor-alpha primed neutrophils, which included reactive oxygen species (ROS) generation, degranulation, secretion of interleukin-8 and activation of p38 and ERK1/2 MAPKs. mtdamps 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 343-356 25817163-8 2015 Interestingly, pharmacological inhibition of p38 or ERK1/2 either alone or in combination significantly inhibited L-selectin shedding and IL-8 secretion by mtDAMP-challenged neutrophils, revealing for the first time that MAPK activation is required for mtDAMP-induced neutrophil activation and function. mtdamp 156-162 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 25433806-7 2015 Furthermore, the inhibition of PCA on LPS-induced IL-6 and IL-8 production can be reversed by PPAR-gamma antagonist GW9662. 2-chloro-5-nitrobenzanilide 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 25471891-0 2015 Piperine Suppresses the Expression of CXCL8 in Lipopolysaccharide-Activated SW480 and HT-29 Cells via Downregulating the Mitogen-Activated Protein Kinase Pathways. piperine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 25471891-5 2015 Importantly, piperine dose-dependently suppressed LPS-induced secretion of CXCL8 and the expression of CXCL8 messenger RNA (mRNA). piperine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 75-80 25471891-5 2015 Importantly, piperine dose-dependently suppressed LPS-induced secretion of CXCL8 and the expression of CXCL8 messenger RNA (mRNA). piperine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 103-108 25471891-8 2015 Collectively, our results indicated that piperine could attenuate the inflammatory response in epithelial cells via downregulating the MAPK signaling and thus the expression of CXCL8, suggesting its potential application in anti-inflammation therapy. piperine 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 177-182 24806275-2 2015 The goal of this study was to investigate the potential for Mn(2+), via its pro-oxidative properties, to activate production of pro-inflammatory cytokines/chemokines IL-1beta, IL-6, IL-8, IFNgamma, TNFalpha, and G-CSF by human monocyte-derived macrophages in vitro. Manganese(2+) 60-66 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 26054185-4 2015 The positive control dentifrice contained 1450 ppm fluoride as sodium fluoride (NaF), in a silica base. silica base 91-102 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 24806275-5 2015 Exposure of the cells to LPS caused modest statistically insignificant increases in cytokine production; MnCl2 caused dose-related increases in production of all six cytokines (achieving statistical significance of p < 0.0171- < 0.0005 for IL-1beta, IL-6, IL-8, IFNgamma, and TNFalpha). manganese chloride 105-110 C-X-C motif chemokine ligand 8 Homo sapiens 262-266 24806275-6 2015 In the case of LPS and MnCl2 combinations, the observed increases in production of IL-1beta, IL-6, IL-8, IFNgamma, and G-CSF were greater than those seen with cells exposed to the individual agents. manganese chloride 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 26634216-7 2015 Hydroxy-3-methoxyaceto-phenone (HMAP), diphenyleneiodonium (DPI), and siRNA Nox2 reduced the ROS and IL-8 release in neutrophils treated with fMLP. hydroxy-3-methoxyaceto-phenone 0-30 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 26634216-7 2015 Hydroxy-3-methoxyaceto-phenone (HMAP), diphenyleneiodonium (DPI), and siRNA Nox2 reduced the ROS and IL-8 release in neutrophils treated with fMLP. diphenyleneiodonium 39-58 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 26634216-7 2015 Hydroxy-3-methoxyaceto-phenone (HMAP), diphenyleneiodonium (DPI), and siRNA Nox2 reduced the ROS and IL-8 release in neutrophils treated with fMLP. diphenyleneiodonium 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 26634216-10 2015 We showed that IL-8 release induced by fMLP is dependent on NADPH oxidase, and ROS could play a redundant role in cell signalling, ultimately activating the PI3K/Akt and NF-kappaB pathways in neutrophils. ros 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 26328410-4 2015 Nanotube diameter and layer changed with different concentration of NaF in 1 M H3PO4 at the same voltage. phosphoric acid 79-84 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 26039682-8 2015 Particles from both Pb-containing and Pb-free ammunition were able to induce oxidative stress and the proinflammatory marker interleukin (IL)-8 in both in vitro systems. Lead 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 125-143 26609426-0 2015 Effects of Lutein and Zeaxanthin on LPS-Induced Secretion of IL-8 by Uveal Melanocytes and Relevant Signal Pathways. Zeaxanthins 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 26609426-8 2015 The present study demonstrated that lutein and zeaxanthin inhibited LPS-induced secretion of IL-8 in cultured UM via JNK and NF-kappaB signal pathways. Zeaxanthins 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 25506634-3 2015 Under the cell-free condition, CB and TiO2 NP showed a high adsorption affinity for IL-8 in supernatants of both lipopolysaccharide (LPS)-stimulated and unstimulated A549 cells. titanium dioxide 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 26039682-8 2015 Particles from both Pb-containing and Pb-free ammunition were able to induce oxidative stress and the proinflammatory marker interleukin (IL)-8 in both in vitro systems. Lead 38-40 C-X-C motif chemokine ligand 8 Homo sapiens 125-143 25653478-6 2015 We found that THC suppressed the release of proinflammatory factors, including tumor necrosis factor alpha (TNF-alpha), interleukin- (IL-) 1beta, IL-6, and IL-8, decreased nuclear factor-kappaB (NF-kappaB) expression, and inhibited the upregulation of cofilin-1 protein in the LPS-stimulated MG-63 cells. Dronabinol 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 25605997-0 2015 Peptidoglycan Induces the Production of Interleukin-8 via Calcium Signaling in Human Gingival Epithelium. Calcium 58-65 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 25605997-3 2015 The triggering of calcium signaling induces the secretion of pro-inflammatory cytokines such as interleukin-8 as part of the inflammatory response; however, the exact mechanism of calcium signaling induced by bacterial toxins when gingival epithelial cells are exposed to pathogens is unclear. Calcium 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 25605997-3 2015 The triggering of calcium signaling induces the secretion of pro-inflammatory cytokines such as interleukin-8 as part of the inflammatory response; however, the exact mechanism of calcium signaling induced by bacterial toxins when gingival epithelial cells are exposed to pathogens is unclear. Calcium 180-187 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 25605997-7 2015 Peptidoglycan-mediated interleukin-8 expression was blocked by U73122 and 1,2-bis(2-aminophenoxy)ethane-N,N,N",N"-tetraacetic acid tetrakis (acetoxymethyl ester). 1,2-bis(2-aminophenoxy)ethane-n,n,n",n"-tetraacetic acid tetrakis (acetoxymethyl ester 74-160 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 25605997-8 2015 Moreover, interleukin-8 expression was induced by thapsigargin, a selective inhibitor of the sarco/endoplasmic reticulum calcium ATPase, when thapsigargin was treated alone or co-treated with peptidoglycan. Thapsigargin 50-62 C-X-C motif chemokine ligand 8 Homo sapiens 10-23 25605997-8 2015 Moreover, interleukin-8 expression was induced by thapsigargin, a selective inhibitor of the sarco/endoplasmic reticulum calcium ATPase, when thapsigargin was treated alone or co-treated with peptidoglycan. Thapsigargin 142-154 C-X-C motif chemokine ligand 8 Homo sapiens 10-23 25605997-9 2015 These results suggest that the gram-positive bacterial toxin peptidoglycan induces calcium signaling via the phospholipase C/inositol 1,4,5-trisphosphate pathway, and that increased interleukin-8 expression is mediated by intracellular calcium levels in human gingival epithelial cells. Calcium 236-243 C-X-C motif chemokine ligand 8 Homo sapiens 182-195 25925366-10 2015 We demonstrate that the experimental use of naturally occurring plant diterpenes such as gibberellin on lipopolysaccharide-stimulated cell lines reduces IL-8 release in an A20-dependent manner. Diterpenes 70-80 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 25925366-10 2015 We demonstrate that the experimental use of naturally occurring plant diterpenes such as gibberellin on lipopolysaccharide-stimulated cell lines reduces IL-8 release in an A20-dependent manner. Gibberellins 89-100 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 26600671-8 2015 In HaCaT keratinocytes histamine and TNF-alpha induced IL-8 and MMP-1 expression was reduced by amarogentin to a similar extent as with azelastine. Histamine 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 25977597-3 2015 In this study, we wanted to assess the efficacy of both low and high doxycycline doses in modulating IL-8, TNF-alpha, and IL-6 gene expression in HaCaT cells stimulated with LPS. Doxycycline 69-80 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 26556954-3 2015 RAFLS incubated with CoCl2, but not S1P, produced less IL-8 and MCP-1 than normal FLS. cobaltous chloride 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 26640326-8 2015 PM10-mediated Ca(2+) signal and IL-8 expression were attenuated by several pharmacological blockades such as antioxidants, IP3-PLC blockers, and TRPM2 inhibitors. Inositol 1,4,5-Trisphosphate 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 25405261-4 2015 There were major differences between the types of NMs; exposure to ZnO and Ag resulted in cytotoxicity and increased gene expression levels of HMOX1 and IL8. Zinc Oxide 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 26652669-5 2015 Rapamycin treatment induced the upregulation of cytokine genes, including those from the Interleukin (IL)-6 signaling network, such as IL-8 and the Leukemia Inhibitory Factor (LIF), while quiescent fibroblasts demonstrated up-regulation of genes involved in the complement and coagulation cascade. Sirolimus 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 25124219-4 2015 The aim of this study was to evaluate the functional relationship between the activity of arterial mineral deposition and regional bone metabolism as assessed by (18)F-sodium fluoride (NaF) PET/CT. Sodium Fluoride 168-183 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 25500537-8 2015 S-CMC treatment increased HDAC2 recruitment and suppressed H4 acetylation of the IL-8 promoter, and this effect was further ablated by addition of buthionine sulfoximine, a specific inhibitor of GSH synthesis. Buthionine Sulfoximine 147-169 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 25500537-8 2015 S-CMC treatment increased HDAC2 recruitment and suppressed H4 acetylation of the IL-8 promoter, and this effect was further ablated by addition of buthionine sulfoximine, a specific inhibitor of GSH synthesis. Glutathione 195-198 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 25998443-5 2015 METHODS: The effect of ambroxol and/or beclomethasone dipropionate on IL-8, RANTES and iNOS levels was assessed by Western blot analysis; IL-8, MPO and 3-NT levels were measured by ELISA. Ambroxol 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 25791156-7 2015 Hydrogen peroxide (H2O2), cytomix (tumour necrosis factor-alpha + IL-1beta + interferon-gamma) and lipopolysaccharide (LPS) upregulated IL-8 mRNA at 1 or 2 h. p38 MAPKalpha mRNA was significantly increased after H2O2 and LPS treatment. Hydrogen Peroxide 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 25998443-5 2015 METHODS: The effect of ambroxol and/or beclomethasone dipropionate on IL-8, RANTES and iNOS levels was assessed by Western blot analysis; IL-8, MPO and 3-NT levels were measured by ELISA. Beclomethasone 39-66 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 25791156-7 2015 Hydrogen peroxide (H2O2), cytomix (tumour necrosis factor-alpha + IL-1beta + interferon-gamma) and lipopolysaccharide (LPS) upregulated IL-8 mRNA at 1 or 2 h. p38 MAPKalpha mRNA was significantly increased after H2O2 and LPS treatment. Hydrogen Peroxide 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 25998443-8 2015 Ambroxol suppressed LPS-induced RANTES expression and IL-8 release (p < 0.001), whilst inhibiting iNOS expression (p < 0.05). Ambroxol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 25791156-7 2015 Hydrogen peroxide (H2O2), cytomix (tumour necrosis factor-alpha + IL-1beta + interferon-gamma) and lipopolysaccharide (LPS) upregulated IL-8 mRNA at 1 or 2 h. p38 MAPKalpha mRNA was significantly increased after H2O2 and LPS treatment. Hydrogen Peroxide 212-216 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 25998443-9 2015 Beclomethasone dipropionate had no effect on RANTES but halved iNOS expression and IL-8 release. Beclomethasone 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 25998443-4 2015 OBJECTIVES: We evaluated the ability of ambroxol and/or beclomethasone dipropionate to inhibit LPS-induced expression/release of RANTES, IL-8, inducible NO synthase (iNOS), myeloperoxidase (MPO) and 3-nitrotyrosine (3-NT: nitrosative stress biomarker) in BEAS-2B +- PMNs stimulated with LPS (1 mug/ml). Ambroxol 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 25998443-11 2015 Ambroxol and beclomethasone dipropionate inhibited LPS-stimulated IL-8, MPO and 3-NT release (p < 0.05). Ambroxol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 25998443-11 2015 Ambroxol and beclomethasone dipropionate inhibited LPS-stimulated IL-8, MPO and 3-NT release (p < 0.05). Beclomethasone 13-40 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 25998443-12 2015 Ambroxol/beclomethasone dipropionate combination potentiated the inhibition of IL-8 and 3-NT production in BEAS-2B with PMNs (p < 0.05 and p < 0.01, respectively). Ambroxol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 79-89 25998443-12 2015 Ambroxol/beclomethasone dipropionate combination potentiated the inhibition of IL-8 and 3-NT production in BEAS-2B with PMNs (p < 0.05 and p < 0.01, respectively). Beclomethasone 9-36 C-X-C motif chemokine ligand 8 Homo sapiens 79-89 25998443-14 2015 CONCLUSION: The additive effect of ambroxol and beclomethasone dipropionate on IL-8 and 3-NT inhibition suggests new therapeutic options in the treatment of neutrophil-related respiratory diseases such as chronic obstructive pulmonary disease and respiratory infections. Ambroxol 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 79-89 25998443-14 2015 CONCLUSION: The additive effect of ambroxol and beclomethasone dipropionate on IL-8 and 3-NT inhibition suggests new therapeutic options in the treatment of neutrophil-related respiratory diseases such as chronic obstructive pulmonary disease and respiratory infections. Beclomethasone 48-75 C-X-C motif chemokine ligand 8 Homo sapiens 79-89 25884029-7 2015 VEGF and IL-8 correlated positively with LDH and PAI-1/tPA ratio and negatively with tPA in both loculated and nonloculated TBPE. Tetradecanoylphorbol Acetate 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 25475379-1 2015 The use of (18)F-sodium fluoride ((18)F-NaF) with PET/CT is increasing. Sodium Fluoride 17-32 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 25884029-7 2015 VEGF and IL-8 correlated positively with LDH and PAI-1/tPA ratio and negatively with tPA in both loculated and nonloculated TBPE. Tetradecanoylphorbol Acetate 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 25884029-7 2015 VEGF and IL-8 correlated positively with LDH and PAI-1/tPA ratio and negatively with tPA in both loculated and nonloculated TBPE. tbpe 124-128 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 25481140-8 2014 Using this method we then calculate the isotropic dipole polarizabilities for F(-), Cl(-), O(2-), and S(2-) embedded in the LiF, LiCl, NaF, NaCl, KF, KCl, ZnO, ZnS, MgO, MgS, CaO, CaS, SrO, SrS, BaO, BaS, and other crystals containing halogen, oxygen, or sulphur anions. dipole 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 135-138 25506832-9 2014 Using PCR we confirmed the significant up-regulation and down-regulation of miR-493-5p and IL8 by imatinib treatment, respectively in K562 cells. Imatinib Mesylate 98-106 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 25506832-12 2014 The IL8 inhibition also further sensitized K562 cells to imatinib cytotoxicity (p < 0.0001). Imatinib Mesylate 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 25540590-0 2014 Differential NF-kappaB and MAPK activation underlies fluoride- and TPA-mediated CXCL8 (IL-8) induction in lung epithelial cells. Fluorides 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 25540590-0 2014 Differential NF-kappaB and MAPK activation underlies fluoride- and TPA-mediated CXCL8 (IL-8) induction in lung epithelial cells. Tetradecanoylphorbol Acetate 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 25540590-0 2014 Differential NF-kappaB and MAPK activation underlies fluoride- and TPA-mediated CXCL8 (IL-8) induction in lung epithelial cells. Tetradecanoylphorbol Acetate 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 25540590-3 2014 To approach this, we compared the potential of the phorbol ester, 12-O-tetradecanoylphorbol-13-acetate (TPA), and sodium fluoride (NaF) to induce CXCL8 responses in A549 cells, with emphasis on the importance of nuclear factor kappa B (NF-kappaB)- and mitogen-activated protein kinase (MAPK) signaling. Phorbol Esters 51-64 C-X-C motif chemokine ligand 8 Homo sapiens 146-151 25540590-3 2014 To approach this, we compared the potential of the phorbol ester, 12-O-tetradecanoylphorbol-13-acetate (TPA), and sodium fluoride (NaF) to induce CXCL8 responses in A549 cells, with emphasis on the importance of nuclear factor kappa B (NF-kappaB)- and mitogen-activated protein kinase (MAPK) signaling. Tetradecanoylphorbol Acetate 66-102 C-X-C motif chemokine ligand 8 Homo sapiens 146-151 25540590-3 2014 To approach this, we compared the potential of the phorbol ester, 12-O-tetradecanoylphorbol-13-acetate (TPA), and sodium fluoride (NaF) to induce CXCL8 responses in A549 cells, with emphasis on the importance of nuclear factor kappa B (NF-kappaB)- and mitogen-activated protein kinase (MAPK) signaling. Tetradecanoylphorbol Acetate 104-107 C-X-C motif chemokine ligand 8 Homo sapiens 146-151 25540590-3 2014 To approach this, we compared the potential of the phorbol ester, 12-O-tetradecanoylphorbol-13-acetate (TPA), and sodium fluoride (NaF) to induce CXCL8 responses in A549 cells, with emphasis on the importance of nuclear factor kappa B (NF-kappaB)- and mitogen-activated protein kinase (MAPK) signaling. Sodium Fluoride 114-129 C-X-C motif chemokine ligand 8 Homo sapiens 146-151 25540590-4 2014 Notably, TPA induced a greater release of CXCL8 than did NaF. Tetradecanoylphorbol Acetate 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 42-47 25608815-4 2015 The results showed that, most of the cytokines or receptors had obvious expression change compared with the control (without Poly I:C stimulation), especially the three cytokine genes IL6, IL8 and IL10, whose average expression change times were 20.71, 10.87 and 5.18, respectively. Poly I-C 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 189-192 25540590-5 2014 Furthermore, TPA induced a strong, rapid, but transient upregulation of CXCL8 messenger (m)RNA, whereas NaF induced a weaker, more delayed, but persistent upregulation. Tetradecanoylphorbol Acetate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 72-77 25540590-10 2014 The CXCL8 responses by TPA and NaF were reduced by p65-siRNA. Tetradecanoylphorbol Acetate 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 4-9 25266909-1 2014 Nitrogen-doped TiO2 nanoparticles have been synthesized using sol-gel methods and subsequently fluorinated at room temperature by aging in acidic solutions of NaF. Nitrogen 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 159-162 25266909-1 2014 Nitrogen-doped TiO2 nanoparticles have been synthesized using sol-gel methods and subsequently fluorinated at room temperature by aging in acidic solutions of NaF. titanium dioxide 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 159-162 25266909-3 2014 After aging at room temperature in NaF solutions, the Ti-OH groups on the surface of the TiO2 nanoparticles were replaced by Ti-F bonds, which resulted in a decrease of the point of zero charge from pH 5.4 to 2.8. titanium dioxide 89-93 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 25378098-2 2014 Reaction is initiated by an electron impacting a helium nanodroplet containing sodium atoms and SF6 molecules, leading to preferential production of energetically favorable structures based on the unit cell of crystalline NaF. Helium 49-55 C-X-C motif chemokine ligand 8 Homo sapiens 222-225 25474105-8 2014 Ramipril reduces mRNA expression of multiple pro-inflammatory cytokines such as IL-1beta, IL-6, IL-8, TNF -alpha, Interferon-[Formula: see text], and MCP-1, as well as aortic wall IL-8 and MCP-1 (P = 0.017 and 0.008, respectively) protein content. Ramipril 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 25474105-8 2014 Ramipril reduces mRNA expression of multiple pro-inflammatory cytokines such as IL-1beta, IL-6, IL-8, TNF -alpha, Interferon-[Formula: see text], and MCP-1, as well as aortic wall IL-8 and MCP-1 (P = 0.017 and 0.008, respectively) protein content. Ramipril 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 25622744-15 2014 CONCLUSION: Dexmedetomidine preconditioning attenuate remote lung injury of lower limb ischemia-reperfusion, and the mechanism may be related to down-regulation of monocytes TLR4 expression and degradation of IL-6, IL-8 and TNF-alpha level. Dexmedetomidine 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 25378098-2 2014 Reaction is initiated by an electron impacting a helium nanodroplet containing sodium atoms and SF6 molecules, leading to preferential production of energetically favorable structures based on the unit cell of crystalline NaF. Sodium 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 222-225 25399576-5 2014 The majority of angiogenic cytokines, including VEGF-A, FGF2, IL-8 and SDF-1alpha, manifest an obligate dependence on heparan sulfate (HS) for their biological activity. Heparitin Sulfate 135-137 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 25268952-6 2014 Along with IL-1beta, exposure to MG-132 and bafilomycin A1 resulted in the secretion of IL-8. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 25268952-6 2014 Along with IL-1beta, exposure to MG-132 and bafilomycin A1 resulted in the secretion of IL-8. bafilomycin 44-55 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 25399576-5 2014 The majority of angiogenic cytokines, including VEGF-A, FGF2, IL-8 and SDF-1alpha, manifest an obligate dependence on heparan sulfate (HS) for their biological activity. Heparitin Sulfate 118-133 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 25312381-4 2014 Sodium fluoride (NaF) had pro-proliferation effects at relatively moderate concentration, with 5 x 10(3) mumol/L having the best effects. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 25312381-9 2014 A BMP specific inhibitor LDN193189 suppressed cell proliferation induced by 5 x 10(3) mumol/L NaF. LDN 193189 25-34 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 25138760-8 2014 RESULTS: Rebamipide suppressed the release of interleukin (IL)-8 and the upregulation of IL-8 mRNA induced by tumour necrosis factor alpha (TNF-alpha) or LPS in corneal fibroblasts. rebamipide 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 46-64 25138760-8 2014 RESULTS: Rebamipide suppressed the release of interleukin (IL)-8 and the upregulation of IL-8 mRNA induced by tumour necrosis factor alpha (TNF-alpha) or LPS in corneal fibroblasts. rebamipide 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 25236743-6 2014 Moreover, we observed that in a first phase, DNFB-induced ATF4 upregulates IL8 mRNA levels while blocking CD86, IL1B, IL12B, and CXL10 transcription. Dinitrofluorobenzene 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 25256070-3 2014 This study investigates the effects of ramipril on the oxidoinflammatory cytokines (IL-6, IL-8, TNF-alpha) and TnT (myocardial injury marker) and their alteration in association with ACE I/D gene polymorphisms. Ramipril 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 25168931-1 2014 The functional imaging technique of dynamic fluorine-18 labeled sodium fluoride positron emission tomography ((18)F-NaF PET) allows the quantitative assessment of regional bone formation by measuring the plasma clearance of fluoride to bone at any site in the skeleton. Fluorine-18 44-55 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 25168931-1 2014 The functional imaging technique of dynamic fluorine-18 labeled sodium fluoride positron emission tomography ((18)F-NaF PET) allows the quantitative assessment of regional bone formation by measuring the plasma clearance of fluoride to bone at any site in the skeleton. Sodium Fluoride 64-79 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 25168931-1 2014 The functional imaging technique of dynamic fluorine-18 labeled sodium fluoride positron emission tomography ((18)F-NaF PET) allows the quantitative assessment of regional bone formation by measuring the plasma clearance of fluoride to bone at any site in the skeleton. Fluorides 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 25251945-6 2014 The beta-glucan-consisting glycans curdlan and zymosan stimulated IL-8 and CCL2 secretion by IEC lines. beta-Glucans 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 25251945-6 2014 The beta-glucan-consisting glycans curdlan and zymosan stimulated IL-8 and CCL2 secretion by IEC lines. Polysaccharides 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 25251945-6 2014 The beta-glucan-consisting glycans curdlan and zymosan stimulated IL-8 and CCL2 secretion by IEC lines. Zymosan 47-54 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 25201328-7 2014 RESULTS: IL-1Ra, IL-6, IL-8, IL-10, IL-15, and MCP-1 were significantly elevated in the PTAA group. ptaa 88-92 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 25384214-6 2014 TANs produced substantial quantities of the proinflammatory factors MCP-1, IL-8, MIP-1alpha, and IL-6, as well as the antiinflammatory IL-1R antagonist. tans 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 25448498-6 2014 Furthermore, clozapine and haloperidol can increase the myeloperoxidase activity and IL-8 production in neutrophils. Clozapine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 25448498-6 2014 Furthermore, clozapine and haloperidol can increase the myeloperoxidase activity and IL-8 production in neutrophils. Haloperidol 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 24999595-0 2014 Silver nanoparticle-induced hMSC proliferation is associated with HIF-1alpha-mediated upregulation of IL-8 expression. Silver 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 25220290-7 2014 RESULTS: The addition of 0.25% CaGP improved the remineralization potential of low-fluoride toothpastes and the NaF as source of fluoride yielded the best results (p<0.001) as evidenced by the hardness analysis. Fluorides 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 25260438-12 2014 CLINICAL SIGNIFICANCE: This study showed that a 1.1% NaF dentifrice (5000ppm) demonstrated greater remineralization ability than the CPP-ACP topical tooth creme and that the addition of fluoride to its formulation seems to enhance remineralization. Fluorides 186-194 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 25335112-0 2014 Berberine hydrochloride IL-8 dependently inhibits invasion and IL-8-independently promotes cell apoptosis in MDA-MB-231 cells. berberine chloride 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 25364454-6 2014 Alterations in carcinoembryonic antigen (CEA), interleukin-8 (IL-8) and cyclooxygenase-2 (COX-2) mRNA expression levels subsequent to pioglitazone treatment were examined in BxPC-3 cells by quantitative reverse transcription polymerase chain reaction. Pioglitazone 134-146 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 25364454-9 2014 Pioglitazone induced CEA mRNA expression, suppressed IL-8 and COX-2 mRNA expression in vitro, and inhibited BxPC-3 xenograft growth. Pioglitazone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 25461914-4 2014 TBBPA enhanced release of interleukin (IL)-6, IL-8, and prostaglandin E2 (PGE2), and suppressed TGF-beta release in HTR-8/SVneo cells. tetrabromobisphenol A 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 25521357-0 2014 Pharmacogenetic interaction analysis of VEGFR-2 and IL-8 polymorphisms in advanced breast cancer patients treated with paclitaxel and bevacizumab. Paclitaxel 119-129 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 25264520-10 2014 Human AEC pre-treated with IL-4 and IL-13, then stimulated with poly I:C, similarly exhibited significantly higher expression of IL8, CXCL9, CXCL10, CXCL11 and CCL5 genes. Poly I-C 64-72 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 25432084-4 2014 Therefore, the aim of this study was to evaluate, in the human lung adenocarcinoma cell line GLC-82, the effects of a 24-hour treatment with simvastatin on hydrogen peroxide (H2O2)-induced changes in cell viability, ERK phosphorylation, matrix metalloproteinase (MMP) expression, innate immunity signaling, NF-kappaB activation and IL-8 secretion. Simvastatin 141-152 C-X-C motif chemokine ligand 8 Homo sapiens 332-336 25257954-3 2014 We found the concentrations of IL-8, TNF-alpha, and TGF-alpha presented in urine were significantly elevated in the high urinary arsenic workers compared with the low urinary arsenic workers. Arsenic 129-136 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 25257954-4 2014 Multiple regression analysis showed that the urinary IL-8 level was significantly positively associated with urinary iAs concentration after adjusting for the confounding effects of age, employed years, body mass index (BMI), smoking, alcohol, and seafood consumption in recent 3 days. Alcohols 235-242 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 25257954-8 2014 These data indicated that arsenic increased the secretion of inflammatory factors and IL-8, TNF-alpha, and TGF-alpha expression may be a useful biomarker of the effect of arsenic exposure. Arsenic 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 25257954-8 2014 These data indicated that arsenic increased the secretion of inflammatory factors and IL-8, TNF-alpha, and TGF-alpha expression may be a useful biomarker of the effect of arsenic exposure. Arsenic 171-178 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 25135357-2 2014 At molecular level, GSNO effects have been shown to modulate the activity of a series of transcription factors (notably NF-kappaB, AP-1, CREB and others) as well as other components of signal transduction chains (e.g. IKK-beta, caspase 1, calpain and others), resulting in the modulation of several cytokines and chemokines expression (TNFalpha, IL-1beta, IFN-gamma, IL-4, IL-8, RANTES, MCP-1 and others). S-Nitrosoglutathione 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 373-377 25399172-3 2014 In this report, we present the measurement of changes of the orientational angle of the "free OH" group at the air/water interface of the sodium fluoride (NaF) solutions at different concentrations using the interface selective sum-frequency generation vibrational spectroscopy (SFG-VS) in the ssp and ppp polarizations. Water 115-120 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 25399172-3 2014 In this report, we present the measurement of changes of the orientational angle of the "free OH" group at the air/water interface of the sodium fluoride (NaF) solutions at different concentrations using the interface selective sum-frequency generation vibrational spectroscopy (SFG-VS) in the ssp and ppp polarizations. Sodium Fluoride 138-153 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 25399172-6 2014 These results provide quantitative molecular details of the ion effects of the NaF salt on the structure of the water molecules at the top-most layer of the air/water interface, even though both the Na(+) cation and the F(-) anion are believed to be among the most excluded ions from the air/water interface. Water 112-117 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 25399172-6 2014 These results provide quantitative molecular details of the ion effects of the NaF salt on the structure of the water molecules at the top-most layer of the air/water interface, even though both the Na(+) cation and the F(-) anion are believed to be among the most excluded ions from the air/water interface. Water 161-166 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 25399172-6 2014 These results provide quantitative molecular details of the ion effects of the NaF salt on the structure of the water molecules at the top-most layer of the air/water interface, even though both the Na(+) cation and the F(-) anion are believed to be among the most excluded ions from the air/water interface. Water 161-166 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 25014275-6 2014 We observed that PGE2 decreased tumor necrosis factor-alpha (TNF-alpha) production evoked by poly(I:C), whereas PGE2 potentiated poly(I:C)-triggered interleukin-8 (IL-8) production. Dinoprostone 112-116 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 25014275-6 2014 We observed that PGE2 decreased tumor necrosis factor-alpha (TNF-alpha) production evoked by poly(I:C), whereas PGE2 potentiated poly(I:C)-triggered interleukin-8 (IL-8) production. Dinoprostone 112-116 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 25452730-7 2014 Using human bronchial epithelial cells, we further show that CS extract (CSE) sequentially activated NADPH oxidase (NADPH oxidase activity, 1.9-fold increase), increased intracellular levels of ROS (3.0-fold increase), activated both MAPKs and NF-kappaB, and induced interleukin-8 (IL-8; 8.2-fold increase); all these CSE-induced events were inhibited by pretreatment with EPA. Cesium 61-63 C-X-C motif chemokine ligand 8 Homo sapiens 267-280 25452730-7 2014 Using human bronchial epithelial cells, we further show that CS extract (CSE) sequentially activated NADPH oxidase (NADPH oxidase activity, 1.9-fold increase), increased intracellular levels of ROS (3.0-fold increase), activated both MAPKs and NF-kappaB, and induced interleukin-8 (IL-8; 8.2-fold increase); all these CSE-induced events were inhibited by pretreatment with EPA. Cesium 61-63 C-X-C motif chemokine ligand 8 Homo sapiens 282-286 25452730-8 2014 Our findings suggest a novel role for EPA in alleviating the oxidative stress and lung inflammation induced by subchronic CS exposure in vivo and in suppressing the CSE-induced IL-8 in vitro via its antioxidant function and by inhibiting MAPKs/NF-kappaB signaling. Eicosapentaenoic Acid 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 25432084-4 2014 Therefore, the aim of this study was to evaluate, in the human lung adenocarcinoma cell line GLC-82, the effects of a 24-hour treatment with simvastatin on hydrogen peroxide (H2O2)-induced changes in cell viability, ERK phosphorylation, matrix metalloproteinase (MMP) expression, innate immunity signaling, NF-kappaB activation and IL-8 secretion. Hydrogen Peroxide 156-173 C-X-C motif chemokine ligand 8 Homo sapiens 332-336 25432084-7 2014 Our results show that simvastatin (30 muM) significantly (P <0.01) inhibited the proliferative effect of H2O2 (0.5 mM) and its stimulatory actions on ERK1/2 phosphorylation, NF-kappaB activation and IL-8 production. Simvastatin 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 25432084-7 2014 Our results show that simvastatin (30 muM) significantly (P <0.01) inhibited the proliferative effect of H2O2 (0.5 mM) and its stimulatory actions on ERK1/2 phosphorylation, NF-kappaB activation and IL-8 production. Hydrogen Peroxide 108-112 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 25089799-7 2014 Bcl3 expression is regulated by bortezomib (BZ)-mediated proteasome inhibition, and BZ inhibits Bcl3 recruitment to its target promoters, resulting in decreased expression of cIAP1 and cIAP2, but increased expression of IL-8 and IL-17. Bortezomib 84-86 C-X-C motif chemokine ligand 8 Homo sapiens 220-224 25390653-5 2014 Simplexide induces a concentration- and time-dependent release of IL-6, CXCL8, TNF-alpha and IL-10 and increases the expression of IL6, CXCL8 and IL10 mRNA. simplexide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 72-77 25390653-5 2014 Simplexide induces a concentration- and time-dependent release of IL-6, CXCL8, TNF-alpha and IL-10 and increases the expression of IL6, CXCL8 and IL10 mRNA. simplexide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 136-141 25352548-3 2014 In human epithelial DLD-1 and monocytic Mono Mac 6 cells resveratrol decreased the expression of iNOS, IL-8 and TNF-alpha by reducing mRNA stability without inhibition of the promoter activity. Resveratrol 57-68 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 25352548-10 2014 Finally, resveratrol incubation enhanced its intra-cellular binding to the IL-8, iNOS and TNF-alpha mRNA. Resveratrol 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 24629538-12 2014 Activated proinflammatory pathways, in particular, IL-8 and IL-1beta, were positively correlated with alcohol consumption and alcohol-craving scores. Alcohols 102-109 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 24629538-12 2014 Activated proinflammatory pathways, in particular, IL-8 and IL-1beta, were positively correlated with alcohol consumption and alcohol-craving scores. Alcohols 126-133 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 25261480-5 2014 Vizantin induced the release of IL-8 when HEK293T cells were transiently cotransfected with TLR-4 and MD-2, but not when they were transfected with TLR-4 or MD-2 alone or with TLR-2 or TLR-2/MD-2. 6,6'-bis-O-(3-nonyldodecanoyl)-alpha,alpha'-trehalose 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 25288184-5 2014 Synthetic modifications of the quinazoline scaffold at the 2 and 4 positions revealed trends in structure-activity relationships with respect to TLR dependent production of the NF-kappaB associated cytokine IL-8 in human peripheral blood mononuclear cells, as well as IL-6 in mouse antigen presenting cells. Quinazolines 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 24796797-5 2014 We found that BP IgG stimulated IL-6 and IL-8 release from HaCaT cells and that non-toxic doses of 17-DMAG inhibited this IL-8, but not IL-6 secretion in a dose- and time-dependent fashion. 17-(dimethylaminoethylamino)-17-demethoxygeldanamycin 99-106 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 25255717-9 2014 RESULTS: Fibrocytes did not affect ASMC proliferation and expression of TGF-beta1, eotaxin, alpha-SMA and MLCK; however, ASMC production of IL-8 and IL-6 was increased in the co-culture and transwell culture by FC. asmc 121-125 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 25255717-10 2014 ASMC treated with FCCM were immunopositive for IL-8/IL-6 and produced more IL-8/IL-6. asmc 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 25255717-10 2014 ASMC treated with FCCM were immunopositive for IL-8/IL-6 and produced more IL-8/IL-6. asmc 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 25255717-10 2014 ASMC treated with FCCM were immunopositive for IL-8/IL-6 and produced more IL-8/IL-6. fccm 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 25255717-10 2014 ASMC treated with FCCM were immunopositive for IL-8/IL-6 and produced more IL-8/IL-6. fccm 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 25255717-11 2014 Furthermore, siRNA silencing of NF-kappaB-p65 or ERK1/2 in transwell cultures of asthmatic ASMC with normal subject FC decreased IL-8 and IL-6 production. asmc 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 25255717-12 2014 CONCLUSIONS AND CLINICAL RELEVANCE: Fibrocytes promoted IL-8 and IL-6 production by ASMC, demonstrating a proinflammatory role for FC and a possible mechanism of the inflammatory phenotype in asthma. asmc 84-88 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 25673551-4 2014 In BV the overgrowth of anaerobes produces noxious substances like polyamines and other compounds that trigger the release of pro-inflammatory cytokines interleukin (IL)-1 beta and IL-8. Polyamines 67-77 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 24890258-0 2014 Zerumbone suppresses IL-1beta-induced cell migration and invasion by inhibiting IL-8 and MMP-3 expression in human triple-negative breast cancer cells. zerumbone 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 24610641-3 2014 We found that expression of the tumor-promoting cytokines, IL-8 and VEGF, induced by hypoxia (<1% O2) and deferoxamine (a hypoxia mimetic) was significantly attenuated in PPARdelta-deficient HCT116 colon cancer cells. Oxygen 101-103 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 24610641-3 2014 We found that expression of the tumor-promoting cytokines, IL-8 and VEGF, induced by hypoxia (<1% O2) and deferoxamine (a hypoxia mimetic) was significantly attenuated in PPARdelta-deficient HCT116 colon cancer cells. Deferoxamine 109-121 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 24691111-6 2014 In all, 3"-, 4-, and 6"-galactosyllactoses of cHMOSs account for specific immunomodulation of polyinosinic:polycytodylic acid-induced IL-8 levels. polycytodylic acid 107-125 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 25134454-6 2014 By blocking the translocation of nuclear factor kappaB to the nucleus, carotenoids are able to interact with the nuclear factor kappaB pathway and thus inhibit the downstream production of inflammatory cytokines, such as interleukin-8 or prostaglandin E2. Carotenoids 71-82 C-X-C motif chemokine ligand 8 Homo sapiens 221-234 25958540-1 2014 The purpose of this study was to investigate the biocompatibility of Ti-30Nb-7Ta alloy surface decorated with TiO2 nanotubes by anodization in an electrolyte containing 1 M H3PO4 and 0.8 wt.% NaF with an applied voltage of 10 V for 2 h. The anodization was carried out using a scanning potentiostat. SCHEMBL3705488 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 25958540-1 2014 The purpose of this study was to investigate the biocompatibility of Ti-30Nb-7Ta alloy surface decorated with TiO2 nanotubes by anodization in an electrolyte containing 1 M H3PO4 and 0.8 wt.% NaF with an applied voltage of 10 V for 2 h. The anodization was carried out using a scanning potentiostat. titanium dioxide 110-114 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 25175786-8 2014 Following the paclitaxel treatment, a decreased apoptosis and G2 phase ratio, an increased cell migration ratio, and an increased production of IL-8 were found in MyD88-overexpressed A549 cells. Paclitaxel 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 24924589-4 2014 We show that I-BET151 is a potent, selective inhibitor of a number of NF-kB target genes involved in induction of inflammation and cell cycle regulation and downregulates production of cytokines such as IL-6 and IL-8. GSK1210151A 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 25522414-6 2014 RESULTS: We found that venlafaxine and EPA were anti-inflammatory: venlafaxine decreased IL-6, with a trend for decreases of IL-8 and IP-10, while EPA decreased the levels of IL-6, IL-15, IL-1RA, and IP-10. Venlafaxine Hydrochloride 23-34 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25705372-0 2014 Downregulation of IL-8, ECP, and total IgE in the tears of patients with atopic keratoconjunctivitis treated with rebamipide eyedrops. rebamipide 114-124 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 25522414-6 2014 RESULTS: We found that venlafaxine and EPA were anti-inflammatory: venlafaxine decreased IL-6, with a trend for decreases of IL-8 and IP-10, while EPA decreased the levels of IL-6, IL-15, IL-1RA, and IP-10. Eicosapentaenoic Acid 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 25705372-4 2014 In the current study we examined the effect of rebamipide eyedrops on the level of interleukin-8 (IL-8), eosinophil cationic protein (ECP), and total IgE on the ocular surface. rebamipide 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 25705372-7 2014 The level of IL-8, ECP, and total IgE in the tears of AKC patients was reduced significantly 4-6 weeks after the start of rebamipide treatment. rebamipide 122-132 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 25288725-3 2014 The molecular basis of biological activation of CIPKs relies on the calcium-dependent interaction of a self-inhibitory NAF motif with a particular CBL, the phosphorylation of the activation loop by upstream kinases, and the subsequent phosphorylation of the CBL by the CIPK. Calcium 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 119-122 25279810-1 2014 Highly selective and sensitive fluorescent probes with a quaternary ammonium moiety have been rationally designed and developed for fast and sensitive fluorescence detection of fluoride ion (F(-) from NaF, not TBAF) in aqueous solution and living cells. quaternary ammonium 57-76 C-X-C motif chemokine ligand 8 Homo sapiens 201-204 25279810-1 2014 Highly selective and sensitive fluorescent probes with a quaternary ammonium moiety have been rationally designed and developed for fast and sensitive fluorescence detection of fluoride ion (F(-) from NaF, not TBAF) in aqueous solution and living cells. Fluorides 177-185 C-X-C motif chemokine ligand 8 Homo sapiens 201-204 25288725-8 2014 Taken all together, we postulate the basis for a conserved calcium-dependent NAF-mediated regulation of CIPKs and a variable regulation by upstream kinases. Calcium 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 24965369-0 2014 Increased expression of dopamine receptors in synovial fibroblasts from patients with rheumatoid arthritis: inhibitory effects of dopamine on interleukin-8 and interleukin-6. Dopamine 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 142-155 25323788-5 2014 The inflammatory-related cytokines interleukin (IL)-1beta, IL-6 and IL-8 were detected after pretreatment with the alpha1/beta2-AR blockers phentolamine/propranolol, both in vitro and in vivo. Phentolamine 140-152 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 25150062-7 2014 HDE-induced IL-6, and IL-8 release was significantly lower in cells that were pretreated with 8-Br-cAMP (P < 0.05). 8-Bromo Cyclic Adenosine Monophosphate 94-103 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 25303153-5 2014 Fluctuating glucose concentrations maximally upregulated TLR4 but not TLR2 expression with increased NF-kB activation, IL-8 and ICAM-1 expression. Glucose 12-19 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 25190815-6 2014 Interestingly, gene silencing of STIM1 or Orai1 also interrupts the activation of calcineurin/nuclear factor of activated T-cells (NFAT) pathway and the production of interleukin 8 triggered by histamine in HUVECs. Histamine 194-203 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 25107704-8 2014 Instead, archazolid caused endoplasmic reticulum (ER) stress response visualized by increased BiP expression and accumulation of IL-8 (and TNF-alpha) at the ER, indicating a perturbation of protein secretion. archazolid 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 25275309-3 2014 Exposure of cells to sphingosine 1-phosphate induced pro-inflammatory responses characterized by interleukin-6, interleukin-8, and cyclooxygenase-2 up-regulations, as observed by ELISA and Western blot. sphingosine 1-phosphate 21-44 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 25056289-6 2014 Furthermore, as little as 5 muM L-K6 significantly inhibited lipopolysaccharide (LPS)- and interleukin-1beta-induced productions of interleukin-8 and tumor necrosis factor-alpha from THP-1 monocytic cells. l-k6 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 132-177 24965369-8 2014 SFs from patients with RA, in comparison with those from patients with OA, showed increased expression of dopamine receptors D1 and D5 , and exogenous dopamine strongly inhibited the production of IL-8 in patients with RA. SFS 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 25023990-11 2014 L+E+P also inhibits the angiogenic factors interleukin-8 and vascular endothelial growth factor as well as their induced signaling pathways in ECs. l+e+p 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 43-56 25272089-5 2014 The results showed that MAG suppressed TNF-alpha-induced chemokine (including CXCL8, CX3CL1, and CXCL16) mRNA expression in HMEC-1 cells, in a dose-dependent manner, and reduced the secretion of these chemokines in culture supernatant. mag 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 25062958-7 2014 Exposure to spermine NONOate, 8-bromo-cGMP, or sildenafil (a phosphodiesterase type 5 inhibitor) also increased the expression of beta-catenin-dependent transcripts, IL-8, and cyclin D1. Sildenafil Citrate 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 25218171-8 2014 In conclusion, ROS activate NF-kappaB and IL-8 induction in DSCR1-transfected cells in a calcium-dependent manner, which is augmented by IL-1beta since IL-1beta increases calcium and ROS levels in the cells. Calcium 171-178 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 25042033-8 2014 Comparatively stronger associations were observed between nitrite, eosinophil cationic protein, leukotrienes C/D/E4 and interleukin-8 in sputum. Nitrites 58-65 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 25042033-8 2014 Comparatively stronger associations were observed between nitrite, eosinophil cationic protein, leukotrienes C/D/E4 and interleukin-8 in sputum. Leukotrienes 96-108 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 25111853-2 2014 However, a previous study showed that dexamethasone inhibited interleukin 8 (IL-8) expression by promoting IL-8 mRNA decay, which implies a posttranscriptional regulation. Dexamethasone 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 25111853-2 2014 However, a previous study showed that dexamethasone inhibited interleukin 8 (IL-8) expression by promoting IL-8 mRNA decay, which implies a posttranscriptional regulation. Dexamethasone 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 25111853-2 2014 However, a previous study showed that dexamethasone inhibited interleukin 8 (IL-8) expression by promoting IL-8 mRNA decay, which implies a posttranscriptional regulation. Dexamethasone 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 25111853-3 2014 Nevertheless, by which mechanism dexamethasone destabilized IL-8 mRNA was unclear. Dexamethasone 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 25062958-7 2014 Exposure to spermine NONOate, 8-bromo-cGMP, or sildenafil (a phosphodiesterase type 5 inhibitor) also increased the expression of beta-catenin-dependent transcripts, IL-8, and cyclin D1. spermine nitric oxide complex 12-28 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 25062958-7 2014 Exposure to spermine NONOate, 8-bromo-cGMP, or sildenafil (a phosphodiesterase type 5 inhibitor) also increased the expression of beta-catenin-dependent transcripts, IL-8, and cyclin D1. 8-bromocyclic GMP 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 25063444-6 2014 In addition, IL-22 conferred resistance to 5-FU and OXA by inducing IL-8 autocrine expression through STAT3 activation. Fluorouracil 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 25218171-0 2014 Reactive oxygen species mediate IL-8 expression in Down syndrome candidate region-1-overexpressed cells. Reactive Oxygen Species 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 25218171-8 2014 In conclusion, ROS activate NF-kappaB and IL-8 induction in DSCR1-transfected cells in a calcium-dependent manner, which is augmented by IL-1beta since IL-1beta increases calcium and ROS levels in the cells. Reactive Oxygen Species 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 25218171-8 2014 In conclusion, ROS activate NF-kappaB and IL-8 induction in DSCR1-transfected cells in a calcium-dependent manner, which is augmented by IL-1beta since IL-1beta increases calcium and ROS levels in the cells. Calcium 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 25111853-6 2014 So, we speculated that dexamethasone destabilized IL-8 mRNA by upregulating TTP expression. Dexamethasone 23-36 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 25111853-7 2014 Here, we report that dexamethasone reduced IL-8 expression through destabilizing IL-8 mRNA in human pulmonary microvascular endothelial cells (HPMECs). Dexamethasone 21-34 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 25111853-7 2014 Here, we report that dexamethasone reduced IL-8 expression through destabilizing IL-8 mRNA in human pulmonary microvascular endothelial cells (HPMECs). Dexamethasone 21-34 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 25016235-6 2014 Compared to naive platelet supernatants, APS had a higher level of various cytokines, such as IL8, IL17, PDGF and VEGF. aps 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 25478290-9 2014 Reduction of MUC18 serine phosphorylation by inhibiting ERK activity was associated with less production of IL-8 following polyI:C stimulation. Serine 19-25 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 25478290-9 2014 Reduction of MUC18 serine phosphorylation by inhibiting ERK activity was associated with less production of IL-8 following polyI:C stimulation. Poly I-C 123-130 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 24648302-8 2014 In contrast, the extent of reduction in serum IL-8 was significantly greater with placebo versus curcuminoids (p = 0.012). curcuminoids 97-109 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 25942827-4 2014 Formation of the nanotubular oxide surface structure was achieved initially on the Ti-25Ta-xZr alloys by anodization in a 1 M H3PO4 electrolyte containing 0.8 wt.% NaF at room temperature, using a potentiostat. Oxides 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 164-167 24754833-0 2014 Calcium phosphate particles induce interleukin-8 expression in a human gingival epithelial cell line via the nuclear factor-kappaB signaling pathway. calcium phosphate 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 24754833-3 2014 The authors examined the effect of nano/microsized calcium phosphate particles, which may be generated in the process of early precipitation and/or dissolution of calcium phosphate mineral, on the expression of interleukin (IL)-8 in human gingival epithelial cells. calcium phosphate 51-68 C-X-C motif chemokine ligand 8 Homo sapiens 211-229 25110916-2 2014 The yield of the corresponding Hiyama coupling products is high up to around 90% in water and isopropanol under an ambient atmosphere in the presence of KOH and NaF. Water 84-89 C-X-C motif chemokine ligand 8 Homo sapiens 161-164 25074943-6 2014 RESULTS: At days 1 and 3, both groups showed a similar inflammatory response; fluticasone produced lower levels of interleukin-8 compared with budesonide (P < .01). Fluticasone 78-89 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 25035127-7 2014 H2S ratio was positively correlated with St. George"s Respiratory Questionnaire score, sputum neutrophils and IL-6 and IL-8 levels in sputum and serum (p<0.01) but inversely correlated with sputum macrophages (%), FEV1%predicted and FEV1/FVC (p<0.01). Hydrogen Sulfide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 25268596-0 2014 ZFC3H1, a zinc finger protein, modulates IL-8 transcription by binding with celastramycin A, a potential immune suppressor. celastramycin A 76-91 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 25268596-1 2014 Celastramycin A, a small molecule that inhibits the production of antibacterial peptides in an ex vivo culture system of Drosophila, suppresses the TNFalpha-mediated induction of IL-8 in mammalian cells. celastramycin A 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 24997298-4 2014 CS-treated MM6 cells released significant amounts of IL-8 and TNF-alpha into the culture supernatant. Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 25110916-2 2014 The yield of the corresponding Hiyama coupling products is high up to around 90% in water and isopropanol under an ambient atmosphere in the presence of KOH and NaF. 2-Propanol 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 161-164 25090483-1 2014 An efficient method for the synthesis of phosphoric fluoride via oxidative coupling between hydrophosphine oxide and NaF is reported. phosphoric fluoride 41-60 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 25257976-8 2014 RESULTS: Sirolimus significantly suppressed the LPS-induced expression of MCP-1, IL-8, RANTES, MIP-1alpha, and MIP-1beta in the THP-1 cells and human primary monocytes. Sirolimus 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 25257976-11 2014 CONCLUSION: Sirolimus downregulates the expression of chemokines in monocytes, including MCP-1, RANTES, IL-8, MIP-1alpha, and MIP-1beta, by inhibiting the NF-kappaB-p65 and MAPK-p38 signalling pathways. Sirolimus 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 25090483-1 2014 An efficient method for the synthesis of phosphoric fluoride via oxidative coupling between hydrophosphine oxide and NaF is reported. hydrophosphine oxide 92-112 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 25238390-8 2014 In human fetal membranes and myometrium, nobiletin significantly decreased LPS-stimulated expression of pro-inflammatory cytokines (TNF-alpha, IL-1beta, IL-6 and IL-8) and MMP-9 expression and pro-MMP-9 secretion. nobiletin 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 25100733-6 2014 A cluster of AU-rich elements in the 3"-UTR of IL8 was essential to the APOBEC1-mediated increase in IL8 production. Gold 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 25100733-6 2014 A cluster of AU-rich elements in the 3"-UTR of IL8 was essential to the APOBEC1-mediated increase in IL8 production. Gold 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 25254627-2 2014 Here we demonstrate that short-term glutamine restriction triggers an endoplasmic reticulum (ER) stress response that leads to production of the pro-inflammatory chemokine, interleukin-8 (IL-8). Glutamine 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 173-186 25254627-2 2014 Here we demonstrate that short-term glutamine restriction triggers an endoplasmic reticulum (ER) stress response that leads to production of the pro-inflammatory chemokine, interleukin-8 (IL-8). Glutamine 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 25254627-3 2014 Glutamine deprivation-induced ER stress triggers colocalization of autophagosomes, lysosomes and the Golgi into a subcellular structure whose integrity is essential for IL-8 secretion. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 25254627-4 2014 The stimulatory effect of glutamine restriction on IL-8 production is attributable to depletion of tricarboxylic acid cycle intermediates. Glutamine 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 25254627-4 2014 The stimulatory effect of glutamine restriction on IL-8 production is attributable to depletion of tricarboxylic acid cycle intermediates. Tricarboxylic Acids 99-117 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 25254627-5 2014 The protein kinase, mTOR, is also colocalized with the lysosomal membrane clusters induced by glutamine deprivation, and inhibition of mTORC1 activity abolishes both endomembrane reorganization and IL-8 secretion. Glutamine 94-103 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 25243587-5 2014 Activation of P2Y6 receptor by its natural ligand, UDP, or its specific agonist, MRS 2693, led to the production of two proinflammatory cytokines, interleukin (IL)-6 and IL-8. Uridine Diphosphate 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 25234616-9 2014 The immunomodulatory effects of BAP were confirmed by lower levels of IL-1beta, IL-8, and a lower WBC count in the supplemented group in comparison with the control group. benzylaminopurine 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 25193250-11 2014 CONCLUSIONS: Regarding the results of our in vitro study, the risk of further demineralization was significantly reduced with the use of TiF(4) and NaF after bleaching with 38% HP. Hydrogen Peroxide 177-179 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 25243101-8 2014 After Ra-223 therapy initiation her bone pain improved, with corresponding decrease in tumor markers and mixed response in (18)F-FDG PET/CT and (18)F-NaF bone PET/CT. Radium-223 6-12 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 25193250-13 2014 In the case of an intra-oral acidic exposure, the use of topical 1.5% TiF(4) and 2.1% NaF agents might be beneficial after bleaching with 38% HP. Hydrogen Peroxide 142-144 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 24928308-7 2014 Furthermore we could observe an increased expression and secretion of pro-inflammatory cytokines like interleukin (IL)-6, IL-8 and MCP-1 (2.5-, 2.4- and 1.5-fold, respectively) by the sDPP4 treatment. sdpp4 184-189 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 24553997-5 2014 Heamatoxylin & eosin staining of acne lesions demonstrated reductions in inflammation and immunohistochemical staining intensity for interleukin-8. heamatoxylin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 137-150 24553997-5 2014 Heamatoxylin & eosin staining of acne lesions demonstrated reductions in inflammation and immunohistochemical staining intensity for interleukin-8. Eosine Yellowish-(YS) 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 137-150 25229003-0 2014 Prostaglandin E2 Induces IL-6 and IL-8 Production by the EP Receptors/Akt/NF-kappaB Pathways in Nasal Polyp-Derived Fibroblasts. Dinoprostone 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 25229003-1 2014 PURPOSE: Interleukin 6 (IL-6) and IL-8 participate in the pathogenesis of chronic rhinosinusitis with nasal polyps, and their levels are increased by prostaglandin E2 (PGE2) in different cell types. Dinoprostone 150-166 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 25229003-1 2014 PURPOSE: Interleukin 6 (IL-6) and IL-8 participate in the pathogenesis of chronic rhinosinusitis with nasal polyps, and their levels are increased by prostaglandin E2 (PGE2) in different cell types. Dinoprostone 168-172 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 25229003-2 2014 The purposes of this study were to determine whether PGE2 has any effect on the increase in the levels of IL-6 and IL-8 in nasal polyp-derived fibroblasts (NPDFs) and subsequently investigate the possible mechanism of this effect. Dinoprostone 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 25229003-5 2014 To determine the signaling pathway for the expression of PGE2-induced IL-6 and IL-8, PGE2 was treated with Akt and NF-kappaB inhibitors in NPDFs. Dinoprostone 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 25229003-5 2014 To determine the signaling pathway for the expression of PGE2-induced IL-6 and IL-8, PGE2 was treated with Akt and NF-kappaB inhibitors in NPDFs. Dinoprostone 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 25229003-9 2014 RESULTS: PGE2 significantly increased the mRNA and protein expression levels of IL-6 and IL-8 in NPDFs. Dinoprostone 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 25229003-12 2014 The Akt and NF-kappaB inhibitors significantly blocked PGE2-induced expression of IL-6 and IL-8. Dinoprostone 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 25229003-15 2014 These results suggest that signaling pathway for IL-6 and IL-8 expression induced by PGE2 might be a useful therapeutic target for the treatment of nasal polyposis. Dinoprostone 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 25016365-7 2014 RESULTS: Irbesartan reduced concentrations of IL-6, IL-8, CCL2, CXCL5, OPG, OPN and CXCL16 in both atheroma and primary vascular cell culture supernatants. Irbesartan 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 24928308-11 2014 Additionally, the sDPP4-induced upregulation of IL-6 and IL-8 could completely be prevented by the PAR2 silencing. sdpp4 18-23 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 25237168-8 2014 With dexamethasone, upregulation of PGE2, IL-6 and IL-8 was suppressed. Dexamethasone 5-18 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 25426154-2 2014 Therefore, the aim of this study was to investigate fluoride release from three GIs before and after exposure to sodium fluoride (NaF) and acidulated phosphate fluoride (APF). Fluorides 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 24821440-6 2014 In human kidney tubule cells, GB88 inhibited cytokine secretion (IL6, IL8, GM-CSF, TNF-alpha) mediated by PAR2. GB88 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 25183586-4 2014 This study was designed to determine whether cobalt induces a similar inflammatory response to LPS by promoting the expression of IL-8 and CXCL10. Cobalt 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 25183586-6 2014 Cobalt-treated macrophages showed a 60-fold increase in IL-8 mRNA, and an eightfold increase in production of the mature chemokine (both p < 0.001); expression of the CXCL10 gene and protein was also significantly increased by cobalt (both p < 0.001). Cobalt 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 25183586-7 2014 Experiments were also performed in the presence of CLI-095, a TLR4-specific antagonist which abrogated the cobalt-mediated increase in IL-8 and CXCL10 expression. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 25183586-7 2014 Experiments were also performed in the presence of CLI-095, a TLR4-specific antagonist which abrogated the cobalt-mediated increase in IL-8 and CXCL10 expression. Cobalt 107-113 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 25183586-9 2014 These pathways result in increased production of IL-8 and CXCL10, and may be implicated in pseudotumour formation following metal-on-metal replacement. Metals 124-129 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 25183586-9 2014 These pathways result in increased production of IL-8 and CXCL10, and may be implicated in pseudotumour formation following metal-on-metal replacement. Metals 133-138 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 25426154-2 2014 Therefore, the aim of this study was to investigate fluoride release from three GIs before and after exposure to sodium fluoride (NaF) and acidulated phosphate fluoride (APF). Sodium Fluoride 113-128 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 24925806-6 2014 While several inhibitors are available for caspase-1 blocking experiments, in this study we show effects of two commonly used caspase inhibitors: z-VAD-fmk and ac-YVAD-cmk on secretion of pro-inflammatory cytokines: IL-1beta, TNFalpha, IL-8 and IL-6 in whole blood stimulated with LPS. benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone 146-155 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 24558180-6 2014 We also observed 12% and 8% increases in IL-8 associated with an IQR increase in NO2 exposure in lag 3 and over the year before sampling, respectively. Nitrogen Dioxide 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 24980968-9 2014 Iron chelation by excess Ent or Ybt significantly increased Lcn2-induced secretion of IL-8, IL-6, and CCL20. Iron 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 24925806-6 2014 While several inhibitors are available for caspase-1 blocking experiments, in this study we show effects of two commonly used caspase inhibitors: z-VAD-fmk and ac-YVAD-cmk on secretion of pro-inflammatory cytokines: IL-1beta, TNFalpha, IL-8 and IL-6 in whole blood stimulated with LPS. ac-yvad 160-167 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 24925806-7 2014 We demonstrate ac-YVAD-cmk is a specific caspase-1 inhibitor resulting in pronounced decreases in IL-1beta and less suppression of TNFalpha, IL-6 and IL-8, while pan-caspase inhibitor, z-VAD-fmk, only weakly suppressed Il-1beta while acting strongly on the other three cytokines. ac-yvad 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 24874926-0 2014 Continued decline of aqueous interleukin-8 after multiple intravitreal injections of ganciclovir for cytomegalovirus retinitis. Ganciclovir 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 27526527-11 2014 The inhibitory effect by sodium fluoride (NaF) was 5-25% decrease after 24 hours. Sodium Fluoride 25-40 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 25284569-8 2014 Production of IL8 by Phenytoin induced gingival fibroblasts in children was decreased compared to adults (P = 0.02). Phenytoin 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 25284569-9 2014 CONCLUSION: Phenytoin induced gingival fibroblasts of children produce more amounts of IL1beta, PGE2, IL6, TGFbeta and IL8 as compared to adults" fibroblasts. Phenytoin 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 119-122 25208282-3 2014 Sodium fluoride labeled with fluorine 18 (sodium fluoride F 18 [(18)F-NaF]) is a positron-emitting radiopharmaceutical first introduced several decades ago for skeletal imaging. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 25208282-3 2014 Sodium fluoride labeled with fluorine 18 (sodium fluoride F 18 [(18)F-NaF]) is a positron-emitting radiopharmaceutical first introduced several decades ago for skeletal imaging. Fluorine 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 24894820-7 2014 The SIRT1 activator resveratrol enhanced S. pneumoniae-induced gene expression of hBD2 but decreased IL-8 mRNA levels. Resveratrol 20-31 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 24894820-8 2014 Blockade of SIRT1 activity by the SIRT1 inhibitors nicotinamide reduced S. pneumoniae-induced hBD2 mRNA expression but increased its stimulatory effects on IL-8 mRNA. Niacinamide 51-63 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 25157974-11 2014 Finally, there is a significant correlation between the levels of IL-10, IL-4, and IL-8 and formic acid (p<0.05). formic acid 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 25208282-3 2014 Sodium fluoride labeled with fluorine 18 (sodium fluoride F 18 [(18)F-NaF]) is a positron-emitting radiopharmaceutical first introduced several decades ago for skeletal imaging. sodium fluoride f 42-59 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 24904980-0 2014 Calcium signaling and beta2-adrenergic receptors regulate 1-nitropyrene induced CXCL8 responses in BEAS-2B cells. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 24904980-0 2014 Calcium signaling and beta2-adrenergic receptors regulate 1-nitropyrene induced CXCL8 responses in BEAS-2B cells. 1-nitropyrene 58-71 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 24904980-2 2014 In the present study we have investigated the mechanisms of CXCL8 (IL-8) responses induced by 1-nitropyrene (1-NP) in human bronchial epithelial BEAS-2B cells, with focus on the possible importance of Ca(2+)-signaling and activation of beta2-adrenergic receptors (beta2AR). 1-nitropyrene 94-107 C-X-C motif chemokine ligand 8 Homo sapiens 60-65 24904980-2 2014 In the present study we have investigated the mechanisms of CXCL8 (IL-8) responses induced by 1-nitropyrene (1-NP) in human bronchial epithelial BEAS-2B cells, with focus on the possible importance of Ca(2+)-signaling and activation of beta2-adrenergic receptors (beta2AR). 1-nitropyrene 94-107 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 24904980-3 2014 Ca(2+)-chelator treatment obliterated 1-NP-induced CXCL8 (IL-8) responses. 1-nitropyrene 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 51-56 24904980-3 2014 Ca(2+)-chelator treatment obliterated 1-NP-induced CXCL8 (IL-8) responses. 1-nitropyrene 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 25048521-0 2014 Determination of the Al2O3 content in NaF-AlF3-CaF2-Al2O3 melts at 950 C by Raman spectroscopy. Aluminum Oxide 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 25148049-4 2014 This study tested the hypothesis that azithromycin treatment, as an add-on to standard medication, would significantly reduce airway neutrophil and neutrophils chemokine (CXCL8) levels, as well as bacterial load. Azithromycin 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 171-176 25148049-12 2014 Azithromycin treatment resulted in a non-significant reduction in sputum neutrophil proportion, CXCL8 levels and bacterial load. Azithromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 96-101 25148049-15 2014 CONCLUSIONS: In stable COPD with neutrophilic bronchitis, add-on azithromycin therapy showed a trend to reduced severe exacerbations sputum neutrophils, CXCL8 levels and bacterial load. Azithromycin 65-77 C-X-C motif chemokine ligand 8 Homo sapiens 153-158 25048521-5 2014 In addition, we discuss two quantitative models to determine the alumina content from the Raman spectra of the molten NaF-AlF3-CaF2-Al2O3 electrolytes. Aluminum Oxide 65-72 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 25048521-6 2014 Univariate and multivariate approaches are applied to determine both the COx (alumina content) and the CR (NaF/AlF3 molar ratio) by Raman spectroscopy without referring to an additional internal reference of intensity. Chromium 103-105 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 25090413-7 2014 In vitro, exposure of human ameloblast-lineage cells to micromolar levels of both NaF and AlF3 led to a significantly increase in SATB1 protein content, but not levels of Satb1 mRNA, suggesting a fluoride-induced mechanism protecting SABT1 from degradation. Fluorides 196-204 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 24976128-6 2014 Villiaumite (NaF) was found to be the dominant fluoride species in the cladding waste and natrophosphate (Na7F[PO4]2 19H2O) was the dominant species in the blended waste. Sodium Fluoride 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 24577419-14 2014 CONCLUSION: Using NaF-PET osteometabolic changes of CBA and implant-bone-interfaces can be monitored. cba 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 24844442-1 2014 Amorphous silica nanoparticles (SiNPs) have previously been shown to induce marked cytokine (interleukin-6; IL-6 and interleukin-8; CXCL8/IL-8) responses independently of particle uptake in human bronchial epithelial BEAS-2B cells. Silicon Dioxide 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 24844442-1 2014 Amorphous silica nanoparticles (SiNPs) have previously been shown to induce marked cytokine (interleukin-6; IL-6 and interleukin-8; CXCL8/IL-8) responses independently of particle uptake in human bronchial epithelial BEAS-2B cells. Silicon Dioxide 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 132-137 24844442-1 2014 Amorphous silica nanoparticles (SiNPs) have previously been shown to induce marked cytokine (interleukin-6; IL-6 and interleukin-8; CXCL8/IL-8) responses independently of particle uptake in human bronchial epithelial BEAS-2B cells. Silicon Dioxide 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 24844442-7 2014 Overall, our results indicate that Si50-induced IL-6 and CXCL8 responses in BEAS-2B cells were regulated through combined activation of several pathways, including NF-kappaBeta and p38/TACE/TGF-alpha/EGFR signalling. si50 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 57-62 25108547-5 2014 RESULTS: Exposure of lung epithelial cells to HCl resulted in increased expression of intercellular adhesion molecule-1 (ICAM-1) and production of interleukin (IL)-8 at 24 h. The expression of the epithelial markers E-cadherin decreased while the mesenchymal markers vimentin and alpha-smooth muscle actin (alpha-SMA) increased at 24 h and remained high at 48 h. The addition of monocytes augmented the profiles of lower expression of epithelial markers and higher mesenchymal markers accompanied by increased collagen deposition. Hydrochloric Acid 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 147-165 24515724-7 2014 Furthermore, bufalin attenuated the TNF-alpha-induced interleukin-1beta (IL-1beta), IL-6, and IL-8 production in RAFLSs in a concentration-dependent manner. bufalin 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 24779584-5 2014 Expression of IL-8 receptors (CXCR1 and CXCR2) and the LPS receptor TLR4 was similar on neutrophils from young and old subjects, and neutrophils challenged with phorbol-12-myristate-13-acetate (PMA) showed no age-associated differences in ROS or NET production. Tetradecanoylphorbol Acetate 194-197 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 24779584-5 2014 Expression of IL-8 receptors (CXCR1 and CXCR2) and the LPS receptor TLR4 was similar on neutrophils from young and old subjects, and neutrophils challenged with phorbol-12-myristate-13-acetate (PMA) showed no age-associated differences in ROS or NET production. Reactive Oxygen Species 239-242 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 24811947-6 2014 The releases of IL-8 from A549 and TNF-alpha from J774A.1 were significantly correlated to PM size, Zeta potential, endotoxin, major metals, and polycyclic aromatic hydrocarbons. Polycyclic Aromatic Hydrocarbons 145-177 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 24777307-0 2014 Suppressive action of acetate on interleukin-8 production via tubulin-alpha acetylation. Acetates 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 24777307-5 2014 Flagellin stimulation induces IL-8 production in epithelial cells and acetate suppresses this IL-8 production via tubulin-alpha acetylation. Acetates 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 24374727-4 2014 We used a multiplex protein assay to determine the tumor expression levels of the proangiogenic proteins IL-6, IL-8, bFGF, PDGF-BB and VEGF-A in formalin-fixed paraffin-embedded tumors from the MAX clinical trial patients with available tissue samples. Formaldehyde 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 24374727-4 2014 We used a multiplex protein assay to determine the tumor expression levels of the proangiogenic proteins IL-6, IL-8, bFGF, PDGF-BB and VEGF-A in formalin-fixed paraffin-embedded tumors from the MAX clinical trial patients with available tissue samples. Paraffin 160-168 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 24719336-11 2014 PGE2 receptor antagonists dose-dependently inhibited the release of IL-6, IL-8, and PGE2 by IFP-stimulated FLS. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24608042-10 2014 These findings indicated that TAMs may facilitate PTC cell metastasis through CXCL8 and its paracrine interaction with CXCR1/2. tams 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 25297357-9 2014 IL-8 expression had negative correlation with MS components especially with triglyceride and total cholesterol (r=0.5, P<0.001). Triglycerides 76-88 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 25297357-9 2014 IL-8 expression had negative correlation with MS components especially with triglyceride and total cholesterol (r=0.5, P<0.001). Cholesterol 99-110 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24859059-9 2014 Thalidomide analogs 1 and 2 demonstrated more potent activity to suppress expression levels of IL-6, IL-8, TNF-alpha, VEGF165, and MMP-2 than thalidomide. Thalidomide 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 24750048-8 2014 YB, TA and YBTA inhibited TNFalpha by 57.57%, 59.09% and 68.93% and IL-8 production by 48.76%, 47.92% and 51.13% in P. acne-stimulated THP-1 cells, respectively. Ytterbium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 24750048-8 2014 YB, TA and YBTA inhibited TNFalpha by 57.57%, 59.09% and 68.93% and IL-8 production by 48.76%, 47.92% and 51.13% in P. acne-stimulated THP-1 cells, respectively. Tantalum 4-6 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 24750048-8 2014 YB, TA and YBTA inhibited TNFalpha by 57.57%, 59.09% and 68.93% and IL-8 production by 48.76%, 47.92% and 51.13% in P. acne-stimulated THP-1 cells, respectively. ybta 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 24729102-0 2014 Effects of alpha lipoic acid supplementation on serum levels of IL-8 and TNF-alpha in patient with ESRD undergoing hemodialysis. Thioctic Acid 11-28 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 24957686-0 2014 Pristimerin, a natural anti-tumor triterpenoid, inhibits LPS-induced TNF-alpha and IL-8 production through down-regulation of ROS-related classical NF-kappaB pathway in THP-1 cells. pristimerin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 24957686-3 2014 The results showed that pristimerin inhibited the production of TNF-alpha and IL-8 in a dose-dependent manner. pristimerin 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 25201625-11 2014 Furthermore, AhR-ligands alone at high concentrations induced a moderate CXCL8-response, without affecting CCL5, but suppressed both CXCL8 and CCL5-responses by Poly I:C. CONCLUSION: AhR and Arnt may differentially and independently regulate chemokine-responses induced by both inhaled pollutants and pulmonary infections. Poly I 161-167 C-X-C motif chemokine ligand 8 Homo sapiens 133-138 25069913-8 2014 Gln also up-regulated expression of interleukin-6, interleukin-8, MCP-1, MIP-3alpha, CCL2, CCL20, and CXCL1. Glutamine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 25058399-10 2014 LY294002, a PI3K inhibitor, inhibited HPV-16 oncoprotein-induced activation of Akt, P70S6K, and P85S6K, expression of HIF-1alpha, VEGF, and IL-8, and in vitro angiogenesis. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 25201625-7 2014 Yet, constitutively active unligated AhR suppressed both CXCL8 and CCL5, as shown by siRNA knock-down and the AhR antagonist alpha-naphthoflavone. alpha-naphthoflavone 125-145 C-X-C motif chemokine ligand 8 Homo sapiens 57-62 25013374-8 2014 Interestingly, treatment with AGP increased the expression and secretion of endogenous interleukin (IL)-6 and IL-8; however, this effect was inhibited when HCAECs were cotreated with cPA or the synthetic peroxisome proliferator-activator receptor gamma (PPARgamma) antagonist T0070907. cpa 183-186 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 25051116-11 2014 CONCLUSIONS: Out of ten analyzed cytokines and nitric oxide, IL-8 correlated with the observed increase in mitochondrial respiration. Nitric Oxide 47-59 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 25089120-7 2014 IPE secreted IL-8 or MCP-1 in response to Pam3CSK4.3HCl, Poly(I:C), LPS and MALP-2, whereas RPE produced IL-8 only after Poly(I:C), LPS or MALP-2 treatment. ipe 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 25089120-7 2014 IPE secreted IL-8 or MCP-1 in response to Pam3CSK4.3HCl, Poly(I:C), LPS and MALP-2, whereas RPE produced IL-8 only after Poly(I:C), LPS or MALP-2 treatment. poly 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 25089120-8 2014 TLR inhibitors (OxPAPC, CI-095 and chloroquine) blocked IL-8 secretion in Poly(I:C), LPS or MALP-2-treated IPE and RPE. oxidized-L-alpha-1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine 16-22 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 25089120-8 2014 TLR inhibitors (OxPAPC, CI-095 and chloroquine) blocked IL-8 secretion in Poly(I:C), LPS or MALP-2-treated IPE and RPE. ci-095 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 25089120-8 2014 TLR inhibitors (OxPAPC, CI-095 and chloroquine) blocked IL-8 secretion in Poly(I:C), LPS or MALP-2-treated IPE and RPE. Chloroquine 35-46 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 25089120-8 2014 TLR inhibitors (OxPAPC, CI-095 and chloroquine) blocked IL-8 secretion in Poly(I:C), LPS or MALP-2-treated IPE and RPE. ipe 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 25010330-7 2014 Among patients with ANS dysregulation or PE, the expression frequency of CD4+Foxp3+ increased markedly after milrinone treatment, and was associated with reduction of plasma levels IL-6, IL-8 and IL-10. Milrinone 109-118 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 24896229-6 2014 Our lead compound, CX797, inhibited IL8-mediated cAMP signaling and receptor degradation while specifically up-regulating IL8-mediated beta-arrestin-2 recruitment. Cyclic AMP 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 24792438-0 2014 Lysophosphatidic acid-induced IL-8 secretion involves MSK1 and MSK2 mediated activation of CREB1 in human fibroblast-like synoviocytes. lysophosphatidic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 32481974-0 2014 Interleukin-8 gene silencing on pancreatic cancer cells using biodegradable polymer nanoplexes. Polymers 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 24792438-1 2014 Lysophosphatidic acid (LPA) is a pleiotropic lipid mediator that promotes motility, survival, and the synthesis of chemokines/cytokines such as interleukin-8 (IL-8) and interleukin-6 by human fibroblast-like synoviocytes from patients with rheumatoid arthritis (RAFLS). lysophosphatidic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 144-157 24792436-3 2014 Tylvalosin treatment markedly decreased IL-8, IL-6, IL-1beta, PGE2, TNF-alpha and NO levels in vitro and in vivo. tylvalosin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 24844181-5 2014 We show that histone tail acetylation status is modified following DEX administration, through distinct and alternative mechanisms at the promoters of interleukin-8 and interleukin-23. Dexamethasone 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 151-164 24792438-1 2014 Lysophosphatidic acid (LPA) is a pleiotropic lipid mediator that promotes motility, survival, and the synthesis of chemokines/cytokines such as interleukin-8 (IL-8) and interleukin-6 by human fibroblast-like synoviocytes from patients with rheumatoid arthritis (RAFLS). lysophosphatidic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 24792438-1 2014 Lysophosphatidic acid (LPA) is a pleiotropic lipid mediator that promotes motility, survival, and the synthesis of chemokines/cytokines such as interleukin-8 (IL-8) and interleukin-6 by human fibroblast-like synoviocytes from patients with rheumatoid arthritis (RAFLS). lysophosphatidic acid 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 144-157 24792438-1 2014 Lysophosphatidic acid (LPA) is a pleiotropic lipid mediator that promotes motility, survival, and the synthesis of chemokines/cytokines such as interleukin-8 (IL-8) and interleukin-6 by human fibroblast-like synoviocytes from patients with rheumatoid arthritis (RAFLS). lysophosphatidic acid 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 24792438-2 2014 In those cells LPA was reported to induce IL-8 secretion through activation of various signaling pathways including p38 mitogen-activated protein kinase (p38 MAPK), p42/44 MAPK, and Rho kinase. lysophosphatidic acid 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 24792438-4 2014 The silencing of MSKs with small-interfering RNAs and the pharmacological inhibitor of MSKs SB747651A shows a role for both MSK1 and MSK2 in LPA-mediated phosphorylation of CREB at Ser-133 and secretion of IL-8 and MCP-1. SB 747651A 92-101 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 24792438-4 2014 The silencing of MSKs with small-interfering RNAs and the pharmacological inhibitor of MSKs SB747651A shows a role for both MSK1 and MSK2 in LPA-mediated phosphorylation of CREB at Ser-133 and secretion of IL-8 and MCP-1. lysophosphatidic acid 141-144 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 24792438-4 2014 The silencing of MSKs with small-interfering RNAs and the pharmacological inhibitor of MSKs SB747651A shows a role for both MSK1 and MSK2 in LPA-mediated phosphorylation of CREB at Ser-133 and secretion of IL-8 and MCP-1. Serine 181-184 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 24792438-5 2014 Whereas CREB inhibitors have off target effects and increased LPA-mediated IL-8 secretion, the silencing of CREB1 with short hairpin RNA significantly reduced LPA-induced chemokine production in RAFLS. lysophosphatidic acid 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 25091484-7 2014 Cholesterol crystal activation of the NF-kappaB pathway also leads to increased IL-6 and IL-8 expression. Cholesterol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 24597536-2 2014 Here, we investigated the role of three different NSAIDs (naproxen, ibuprofen and oxaprozin) on neutrophil responses to CXCL8 and C5a. Naproxen 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 120-125 24597536-2 2014 Here, we investigated the role of three different NSAIDs (naproxen, ibuprofen and oxaprozin) on neutrophil responses to CXCL8 and C5a. Ibuprofen 68-77 C-X-C motif chemokine ligand 8 Homo sapiens 120-125 24597536-2 2014 Here, we investigated the role of three different NSAIDs (naproxen, ibuprofen and oxaprozin) on neutrophil responses to CXCL8 and C5a. Oxaprozin 82-91 C-X-C motif chemokine ligand 8 Homo sapiens 120-125 24597536-11 2014 Pretreatment with different NSAIDs prevented C5a-induced integrin (CD11b) up-regulation, while only ibuprofen reduced CXCL8-induced CD11b up-regulation. Ibuprofen 100-109 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 24172227-0 2014 Short-term exposure to oleandrin enhances responses to IL-8 by increasing cell surface IL-8 receptors. oleandrin 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 24172227-0 2014 Short-term exposure to oleandrin enhances responses to IL-8 by increasing cell surface IL-8 receptors. oleandrin 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 24172227-4 2014 Here, we studied the effects of the plant glycoside oleandrin on responses to IL-8 in a human monocytic cell line. Glycosides 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 24172227-4 2014 Here, we studied the effects of the plant glycoside oleandrin on responses to IL-8 in a human monocytic cell line. oleandrin 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 24172227-10 2014 Pulse exposure to oleandrin increased expression of IL-8 receptors and chemotaxis, release of enzymes and activation of NF-kappaB, NFAT and AP-1 along with increased IL-8-mediated calcineurin activation, and wound healing. oleandrin 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 24172227-10 2014 Pulse exposure to oleandrin increased expression of IL-8 receptors and chemotaxis, release of enzymes and activation of NF-kappaB, NFAT and AP-1 along with increased IL-8-mediated calcineurin activation, and wound healing. oleandrin 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 24172227-12 2014 CONCLUSIONS AND IMPLICATIONS: Short-term (1 h; pulse) exposure to a toxic glycoside oleandrin, enhanced biological responses to IL-8 in monocytic cells, without cytoxicity. Glycosides 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 24172227-12 2014 CONCLUSIONS AND IMPLICATIONS: Short-term (1 h; pulse) exposure to a toxic glycoside oleandrin, enhanced biological responses to IL-8 in monocytic cells, without cytoxicity. oleandrin 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 24048734-0 2014 In oesophageal squamous cells exposed to acidic bile salt medium, omeprazole inhibits IL-8 expression through effects on nuclear factor-kappaB and activator protein-1. Omeprazole 66-76 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 24925646-5 2014 Leukotriene C4 (LTC4) and LTD4 were used as the agonists to induce IL-8 production and the related changes in signal molecules. Leukotriene C4 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 24858696-0 2014 Dexamethasone modifies mitomycin C-triggered interleukin-8 secretion in isolated human Tenon"s capsule fibroblasts. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 24858696-0 2014 Dexamethasone modifies mitomycin C-triggered interleukin-8 secretion in isolated human Tenon"s capsule fibroblasts. Mitomycin 23-34 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 24858696-6 2014 Recombinant interleukin-8 (IL-8) was used to verify the effect of MMC-related IL-8 secretion. Mitomycin 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 24858696-6 2014 Recombinant interleukin-8 (IL-8) was used to verify the effect of MMC-related IL-8 secretion. Mitomycin 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 24858696-6 2014 Recombinant interleukin-8 (IL-8) was used to verify the effect of MMC-related IL-8 secretion. Mitomycin 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 24858696-13 2014 In contrast, DEX reversed the MMC-retarded cell proliferation rate (p = 0.036) and repressed MMC-related IL-8 secretion by 33.5% at 3 dpt (p = 0.003). Dexamethasone 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 24858696-19 2014 We conclude that DEX reversed the MMC-inhibited HTF cell proliferation via diminishing the MMC-induced IL-8 secretion, which resulted from a late-phase upregulation of the PPARgamma and Bcl-xL. Dexamethasone 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 24858696-19 2014 We conclude that DEX reversed the MMC-inhibited HTF cell proliferation via diminishing the MMC-induced IL-8 secretion, which resulted from a late-phase upregulation of the PPARgamma and Bcl-xL. Mitomycin 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 24858696-19 2014 We conclude that DEX reversed the MMC-inhibited HTF cell proliferation via diminishing the MMC-induced IL-8 secretion, which resulted from a late-phase upregulation of the PPARgamma and Bcl-xL. Mitomycin 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 24925646-9 2014 The ERK1/2 inhibitor U0126 inhibited Egr-1 and IL-8 expression as well as IL-8 release, but the JNK and p38 inhibitors did not have the inhibitory effects. U 0126 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 24925646-9 2014 The ERK1/2 inhibitor U0126 inhibited Egr-1 and IL-8 expression as well as IL-8 release, but the JNK and p38 inhibitors did not have the inhibitory effects. U 0126 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24874745-10 2014 Furthermore, orbital tissue was obtained from a patient with active GO, and the effect of dasatinib on the expression levels of HAS2-, CCL2-, IL6-, and IL8-mRNA expression was examined by real-time quantitative PCR. Dasatinib 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 24048734-9 2014 RESULTS: Acidic bile salt medium caused oesophageal epithelial cells to express IL-8 mRNA and protein by activating the IL-8 promoter through NF-kappaB and AP-1 binding. Bile Acids and Salts 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 24874745-14 2014 In orbital tissue from active GO, dasatinib significantly suppressed HAS2-, CCL2-, IL6- and IL8-mRNA levels. Dasatinib 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 24048734-9 2014 RESULTS: Acidic bile salt medium caused oesophageal epithelial cells to express IL-8 mRNA and protein by activating the IL-8 promoter through NF-kappaB and AP-1 binding. Bile Acids and Salts 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 24048734-10 2014 Omeprazole inhibited that acidic bile salt-stimulated IL-8 expression by blocking the nuclear translocation of p65 (an NF-kappaB subunit), and by blocking the binding of p65, c-jun and c-fos (AP-1 subunits) to the IL-8 promoter. Omeprazole 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 24048734-10 2014 Omeprazole inhibited that acidic bile salt-stimulated IL-8 expression by blocking the nuclear translocation of p65 (an NF-kappaB subunit), and by blocking the binding of p65, c-jun and c-fos (AP-1 subunits) to the IL-8 promoter. Omeprazole 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 24048734-10 2014 Omeprazole inhibited that acidic bile salt-stimulated IL-8 expression by blocking the nuclear translocation of p65 (an NF-kappaB subunit), and by blocking the binding of p65, c-jun and c-fos (AP-1 subunits) to the IL-8 promoter. Bile Acids and Salts 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 24048734-10 2014 Omeprazole inhibited that acidic bile salt-stimulated IL-8 expression by blocking the nuclear translocation of p65 (an NF-kappaB subunit), and by blocking the binding of p65, c-jun and c-fos (AP-1 subunits) to the IL-8 promoter. Bile Acids and Salts 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 24048734-12 2014 CONCLUSIONS: In oesophageal squamous epithelial cells, omeprazole inhibits IL-8 expression through effects on NF-kappaB and AP-1 that are entirely independent of effects on gastric acid secretion. Omeprazole 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 25244845-8 2014 In addition, the photocatalytic experiment with the addition of NaF indicated that the adsorption of PFOA was of primary importance for the photocatalytic decomposition. perfluorooctanoic acid 101-105 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 24819422-1 2014 UNLABELLED: The National Oncologic PET Registry prospectively assessed the impact of PET with (18)F-sodium fluoride (NaF PET) on intended management of Medicare patients with suspected or known osseous metastasis. f-sodium fluoride 98-115 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 24788377-10 2014 Similarly, IL-8 levels were markedly increased in the ventilated DL and collapsed NDL after OLV compared with those before OLV in the sevoflurane group, whereas there was no significant change in IL-8 levels in the propofol group in the ventilated DL and collapsed NDL before and after OLV. Sevoflurane 134-145 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 24662521-7 2014 High-glucose conditions further enhanced the tumour-driven macrophage enrichment and associated interleukin (IL)-6 and IL-8 cytokine levels. high-glucose 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 24833491-7 2014 In this work, we provide preliminary evidence that (18)F-NaF PET imaging can be used to detect breast cancer by targeting the hydroxyapatite lattice within the tumor microenvironment with high specificity and soft-tissue contrast-to-background ratio while delineating tumors from inflammation. Durapatite 126-140 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 24857974-7 2014 The chondroprotective action of diacerein in mechanically stimulated cells was mediated by a decrease in interleukin-8 (IL-8), fibronectin-1 (FN-1), collagen type I (Col 1) and MMP-1 expression levels, respectively. diacerein 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 24406841-7 2014 Treatment with ruxolitinib also resulted in the reduction of key cytokines (tumor necrosis factor alpha, interleukin-4 (IL-4), IL-6 and IL-8) and induction of interferon-gamma. ruxolitinib 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 24857974-7 2014 The chondroprotective action of diacerein in mechanically stimulated cells was mediated by a decrease in interleukin-8 (IL-8), fibronectin-1 (FN-1), collagen type I (Col 1) and MMP-1 expression levels, respectively. diacerein 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 25030398-3 2014 Fluorine-18-sodium fluoride (18F-NaF) is a highly sensitive PET tracer used as a marker of osteoblastic abnormalities. fluorine-18-sodium fluoride 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 24847057-7 2014 UDP-Glc also stimulated keratinocyte migration, proliferation, and IL-8 expression, supporting a notion that UDP-Glc signals for epidermal inflammation, enhanced hyaluronan synthesis as an integral part of it. Uridine Diphosphate Glucose 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 24998372-4 2014 RESULTS: Treatment with formoterol and budesonide 72 h before and after RV14 infection reduced RV14 titers and cytokine concentrations, including interleukin (IL)-1beta, IL-6 and IL-8, in supernatants and viral RNA within cells. Formoterol Fumarate 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 24998372-4 2014 RESULTS: Treatment with formoterol and budesonide 72 h before and after RV14 infection reduced RV14 titers and cytokine concentrations, including interleukin (IL)-1beta, IL-6 and IL-8, in supernatants and viral RNA within cells. Budesonide 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 24847057-7 2014 UDP-Glc also stimulated keratinocyte migration, proliferation, and IL-8 expression, supporting a notion that UDP-Glc signals for epidermal inflammation, enhanced hyaluronan synthesis as an integral part of it. Uridine Diphosphate Glucose 109-116 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 24918924-5 2014 RESULTS: In HAEC, TLR4 antagonism with eritoran inhibited LPS-induced mRNA expression of IL-6, IL-8, TNFalpha, CCL-2, VCAM and ICAM (P<0.05 for all) and inhibited Ox-PAPC-induced mRNA expression of IL-8 (P<0.05) and IL-6, albeit not to a statistically significant level (p = 0.07). eritoran 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 24491692-2 2014 Due to an increase of neutrophil mediators in acute myocardial infarction the aim of this study was to establish the effect of oleacein on neutral endopeptidase (NEP) activity and other functions of human neutrophils, such as elastase, MMP-9 and IL-8 production. oleacein 127-135 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 24491692-4 2014 Oleacein with a concentration of 100 muM inhibited NEP activity, elastase, MMP-9 and IL-8 release from neutrophils by 77.7 +- 2.7%, 21.3 +- 7.8%, 22.7 +- 4.2% and 25.2 +- 5.6%, respectively. oleacein 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 25002964-6 2014 RESULTS: Probiotic supplementation was associated with decreased LTA (lipoteichoic acid) induced CCL4, CXCL8, IL-1beta and IL-6 responses at 12 months and decreased CCL4 and IL-1beta secretion at 24 months. lipoteichoic acid 70-87 C-X-C motif chemokine ligand 8 Homo sapiens 103-108 24760988-9 2014 While these results point to potential involvement of PRRs, L-C14 carnitine promoted IL-8 secretion from human epithelial cells (HCT-116) lacking Toll-like receptors (TLR)2 and -4, and did not activate reporter constructs in TLR overexpression cell models. l-c14 carnitine 60-75 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 24867687-5 2014 The NF-kappaB inhibitor DHMEQ inhibited the production of IL-6 and IL-8 by EOC cell lines. dehydroxymethylepoxyquinomicin 24-29 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 24918924-5 2014 RESULTS: In HAEC, TLR4 antagonism with eritoran inhibited LPS-induced mRNA expression of IL-6, IL-8, TNFalpha, CCL-2, VCAM and ICAM (P<0.05 for all) and inhibited Ox-PAPC-induced mRNA expression of IL-8 (P<0.05) and IL-6, albeit not to a statistically significant level (p = 0.07). eritoran 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 24905361-0 2014 Finding ATF4/p75NTR/IL-8 signal pathway in endothelial-mesenchymal transition by safrole oxide. safrole oxide 81-94 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 24522860-4 2014 RESULTS: Activation of M3 mAChR with carbachol increased both IL-8 mRNA and protein expression in a concentration-dependent manner. Carbachol 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 24704898-1 2014 We investigate whether a novel and inexpensive etching method, H3PO4 + NaF, on titanium could obtain both a lower hydrogen content and superior calcium phosphate deposition performance, while achieving similar surface roughness in comparison with the traditional etching method. Titanium 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 24704898-1 2014 We investigate whether a novel and inexpensive etching method, H3PO4 + NaF, on titanium could obtain both a lower hydrogen content and superior calcium phosphate deposition performance, while achieving similar surface roughness in comparison with the traditional etching method. Hydrogen 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 24704898-1 2014 We investigate whether a novel and inexpensive etching method, H3PO4 + NaF, on titanium could obtain both a lower hydrogen content and superior calcium phosphate deposition performance, while achieving similar surface roughness in comparison with the traditional etching method. calcium phosphate 144-161 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 24751922-1 2014 The objective of this study was to locate the functional region responsible for the chemotaxis-inducing activity of flounder interleukin 8 (IL-8), which lacks the glutamic acid-leucine-arginine (ELR) motif essential for the induction of neutrophil migration by mammalian IL-8. glutamic acid-leucine-arginine 163-193 C-X-C motif chemokine ligand 8 Homo sapiens 125-138 24751922-1 2014 The objective of this study was to locate the functional region responsible for the chemotaxis-inducing activity of flounder interleukin 8 (IL-8), which lacks the glutamic acid-leucine-arginine (ELR) motif essential for the induction of neutrophil migration by mammalian IL-8. glutamic acid-leucine-arginine 163-193 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 24751922-8 2014 We propose that residue 6 (leucine) at the N-terminus is important for the chemotaxis-inducing activity of flounder IL-8. Leucine 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 24716633-0 2014 Increased IL-8 production in human bronchial epithelial cells after exposure to azithromycin-pretreated Pseudomonas aeruginosa in vitro. Azithromycin 80-92 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 24716633-4 2014 The results showed that AZM-pretreated P. aeruginosa (PAO1 and six different clinical isolates) significantly stimulated HBE cells to release IL-8, a crucial pro-inflammatory cytokine. Azithromycin 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24716633-6 2014 Our results suggest that AZM-pretreated P. aeruginosa could indirectly exacerbate pro-inflammation by inducing IL-8 production in HBEs. Azithromycin 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 24522860-6 2014 M3 mAChR-mediated IL-8 expression was almost completely inhibited by the NF-kappaB inhibitor BAY11-7082 and, to a lesser extent, by U0126, SB203580, and SP600125, which are inhibitors for ERK1/2, p38, and JNK, respectively. SB 203580 139-147 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 24522860-6 2014 M3 mAChR-mediated IL-8 expression was almost completely inhibited by the NF-kappaB inhibitor BAY11-7082 and, to a lesser extent, by U0126, SB203580, and SP600125, which are inhibitors for ERK1/2, p38, and JNK, respectively. pyrazolanthrone 153-161 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 24522860-7 2014 Furthermore, M3 mAChR-mediated NF-kappaB activation and IL-8 expression were simultaneously attenuated by the PKC inhibitor calphostin C, whereas PMA, a PKC activator, mimicked the effects of carbachol, inducing IL-8 expression. calphostin C 124-136 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 24522860-7 2014 Furthermore, M3 mAChR-mediated NF-kappaB activation and IL-8 expression were simultaneously attenuated by the PKC inhibitor calphostin C, whereas PMA, a PKC activator, mimicked the effects of carbachol, inducing IL-8 expression. calphostin C 124-136 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 24522860-5 2014 Elevated IL-8 expression was completely antagonized by atropine, 4-DAMP and tiotropium. Atropine 55-63 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 24522860-6 2014 M3 mAChR-mediated IL-8 expression was almost completely inhibited by the NF-kappaB inhibitor BAY11-7082 and, to a lesser extent, by U0126, SB203580, and SP600125, which are inhibitors for ERK1/2, p38, and JNK, respectively. 3-(4-methylphenylsulfonyl)-2-propenenitrile 93-103 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 24522860-6 2014 M3 mAChR-mediated IL-8 expression was almost completely inhibited by the NF-kappaB inhibitor BAY11-7082 and, to a lesser extent, by U0126, SB203580, and SP600125, which are inhibitors for ERK1/2, p38, and JNK, respectively. U 0126 132-137 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 24851271-8 2014 At 24 h treatment of hPDLSCs with BzATP it enhanced the release of the pro-inflammatory agents IL8 and CCL20, without influencing cell viability. BzATP 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 24816468-2 2014 Our study involves evaluating the extent to which the pre-treatment of saliva samples with an anionic detergent - sodium dodecyl sulphate (SDS) - improved detection levels for IL-8 and EGF. Sodium Dodecyl Sulfate 114-137 C-X-C motif chemokine ligand 8 Homo sapiens 176-188 24816468-2 2014 Our study involves evaluating the extent to which the pre-treatment of saliva samples with an anionic detergent - sodium dodecyl sulphate (SDS) - improved detection levels for IL-8 and EGF. Sodium Dodecyl Sulfate 139-142 C-X-C motif chemokine ligand 8 Homo sapiens 176-188 24816468-6 2014 We found that pre-treatment of samples with SDS significantly increased the detection levels for both EGF (293%) and IL-8 (346%) when compared with PBS-treated pairs (***P<0.001). Sodium Dodecyl Sulfate 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 24885771-6 2014 In vitro macrophage exposure to representative NP (Fe2O3, Fe3O4, MnFe2O4 and CrOOH) induced the production of a pro-inflammatory secretome (increased production of CXCL-8, IL-1ss, TNF-alpha, CCL-2, -3, -4, and to a lesser extent IL-6, CCL-7 and -22), and all but Fe3O4 NP induce an increased migration of macrophages (Boyden chamber). Iron(III) oxide 51-56 C-X-C motif chemokine ligand 8 Homo sapiens 164-170 24849681-8 2014 Based on a logistic regression analysis, smoker phosphate mine workers have a higher relative risk than controls to have an increase concentration of some cytokines, especially IL-1beta, IL-6, IL-8, TNF-alpha, and MIP-1beta. Phosphates 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 24849681-9 2014 Moreover, the combined effect of smoking and phosphate dusts exposure increases the level of leucocytes as well as the concentration of IL-1beta, IL-6, IL-8, MIP1-beta, and LTB-4. Phosphates 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 24559582-9 2014 CONCLUSIONS: Our results suggest that combination therapy with miglitol and sitagliptin improves glycemic control and reduces the circulating protein concentrations of IL-8, sE-selectin, and sVCAM-1 in type 2 diabetic Japanese patients. Sitagliptin Phosphate 76-87 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 24668612-0 2014 Elevated IL-8, TNF-alpha, and MCP-1 in men with metastatic prostate cancer starting androgen-deprivation therapy (ADT) are associated with shorter time to castration-resistance and overall survival. adt 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 25174381-18 2014 Compared with those detected before treatment, the levels of TNF-alpha, IL-6, and IL-8 in serum of group BP at PTH 24 and 48 were significantly decreased (with P values below 0.01). Benzo(a)pyrene 105-107 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 24879414-11 2014 Angiogenin, IGFBP-1, IL-8, MCP-1, MMP-9, and VEGF mRNA and protein expressions were significantly enhanced in LPA-treated chondrocytes. lysophosphatidic acid 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 24879414-13 2014 Pretreatment with the Gi/o type G protein inhibitor, pertussis toxin (PTX), and the NF-kB inhibitor, PDTC, significantly inhibited LPA-induced angiogenin, IGFBP-1, IL-8, MCP-1, MMP-9, and VEGF expressions in chondrocytes. lysophosphatidic acid 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 24852112-2 2014 These glasses exhibit significant superiority compared with traditional fluorozirconate glass (ZrF4-BaF2-LaF3-AlF3-NaF) because of their higher temperature of glass transition and better resistance to water corrosion. fluorozirconate 72-87 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 25177524-7 2014 Biliverdin (50 muM) significantly decreased the LPS-mediated gene expression of IL-1beta, IL-6, IFN-gamma, IL-1Ra and IL-8 (P<0.05). Biliverdine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 24770886-8 2014 In concert with these results, targeting MUC1-C with GO-203 suppresses IL-8/CXCR1 expression and disrupts the formation of established mammospheres. (arginine)9-cysteinyl-glutaminyl-cysteinyl-arginyl-arginyl-lysyl-asparagine 53-59 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 24828117-11 2014 CONCLUSIONS: Out of ten analyzed cytokines and nitric oxide, IL-8 correlated with the observed increase in mitochondrial respiration. Nitric Oxide 47-59 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 24885771-6 2014 In vitro macrophage exposure to representative NP (Fe2O3, Fe3O4, MnFe2O4 and CrOOH) induced the production of a pro-inflammatory secretome (increased production of CXCL-8, IL-1ss, TNF-alpha, CCL-2, -3, -4, and to a lesser extent IL-6, CCL-7 and -22), and all but Fe3O4 NP induce an increased migration of macrophages (Boyden chamber). manganese ferrite 65-72 C-X-C motif chemokine ligand 8 Homo sapiens 164-170 24819773-7 2014 Our data indicate that IL-8 induced NETosis is reduced by ascomycin and cyclosporine A, antagonists of the calcineurin pathway, but not following treatment with rapamycin, which utilizes the mTOR pathway. immunomycin 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 24819773-7 2014 Our data indicate that IL-8 induced NETosis is reduced by ascomycin and cyclosporine A, antagonists of the calcineurin pathway, but not following treatment with rapamycin, which utilizes the mTOR pathway. Cyclosporine 72-86 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 24885636-8 2014 Furthermore, cytokines that were secreted by TAMs, such as IL-6 and IL-8, were also significantly increased. tams 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 24885771-6 2014 In vitro macrophage exposure to representative NP (Fe2O3, Fe3O4, MnFe2O4 and CrOOH) induced the production of a pro-inflammatory secretome (increased production of CXCL-8, IL-1ss, TNF-alpha, CCL-2, -3, -4, and to a lesser extent IL-6, CCL-7 and -22), and all but Fe3O4 NP induce an increased migration of macrophages (Boyden chamber). crooh 77-82 C-X-C motif chemokine ligand 8 Homo sapiens 164-170 24885636-9 2014 This response was attenuated by treating TAMs with the KCNN4 channel-specific inhibitor, 1-[(2-chlorophenyl) diphenylmethyl]-1H-pyrazole (TRAM-34), which suggested that KCNN4 channels may be involved in inducing the secretion of IL-6 and IL-8 by TAMs and improving CRC cell invasiveness. tams 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 24885636-9 2014 This response was attenuated by treating TAMs with the KCNN4 channel-specific inhibitor, 1-[(2-chlorophenyl) diphenylmethyl]-1H-pyrazole (TRAM-34), which suggested that KCNN4 channels may be involved in inducing the secretion of IL-6 and IL-8 by TAMs and improving CRC cell invasiveness. TRAM 34 89-136 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 24819773-8 2014 The action of the G protein coupled receptor phospholipase C pathway appears to be essential for the induction of NETs by IL-8, as NETosis was diminished by treatment with either pertussis toxin, a G-protein inhibitor, the phospholipase C inhibitor, U73122, or staurosporine, an inhibitor of protein kinase C. The data regarding the calcineurin antagonists, ascomycin and cyclosporine A, open the possibility to therapeutically suppress or modulate NETosis. 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 250-256 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 24819773-8 2014 The action of the G protein coupled receptor phospholipase C pathway appears to be essential for the induction of NETs by IL-8, as NETosis was diminished by treatment with either pertussis toxin, a G-protein inhibitor, the phospholipase C inhibitor, U73122, or staurosporine, an inhibitor of protein kinase C. The data regarding the calcineurin antagonists, ascomycin and cyclosporine A, open the possibility to therapeutically suppress or modulate NETosis. Staurosporine 261-274 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 24819773-8 2014 The action of the G protein coupled receptor phospholipase C pathway appears to be essential for the induction of NETs by IL-8, as NETosis was diminished by treatment with either pertussis toxin, a G-protein inhibitor, the phospholipase C inhibitor, U73122, or staurosporine, an inhibitor of protein kinase C. The data regarding the calcineurin antagonists, ascomycin and cyclosporine A, open the possibility to therapeutically suppress or modulate NETosis. immunomycin 358-367 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 24819773-8 2014 The action of the G protein coupled receptor phospholipase C pathway appears to be essential for the induction of NETs by IL-8, as NETosis was diminished by treatment with either pertussis toxin, a G-protein inhibitor, the phospholipase C inhibitor, U73122, or staurosporine, an inhibitor of protein kinase C. The data regarding the calcineurin antagonists, ascomycin and cyclosporine A, open the possibility to therapeutically suppress or modulate NETosis. Cyclosporine 372-386 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 24885636-9 2014 This response was attenuated by treating TAMs with the KCNN4 channel-specific inhibitor, 1-[(2-chlorophenyl) diphenylmethyl]-1H-pyrazole (TRAM-34), which suggested that KCNN4 channels may be involved in inducing the secretion of IL-6 and IL-8 by TAMs and improving CRC cell invasiveness. TRAM 34 138-145 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 24885636-13 2014 CONCLUSIONS: Our findings suggested that TAMs participate in the metastasis of CRC induced by PRL-3 through the TNF-alpha mediated secretion of IL-6 and IL-8 in a paracrine manner. tams 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 24885871-3 2014 This study examined the effect of linoleate, a member of the n-6 family, on regulation of the palmitate-induced inflammatory cytokine interleukin-8 (IL8) in hepatocytes. Linoleic Acid 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 134-147 24885871-3 2014 This study examined the effect of linoleate, a member of the n-6 family, on regulation of the palmitate-induced inflammatory cytokine interleukin-8 (IL8) in hepatocytes. Linoleic Acid 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 149-152 24885871-3 2014 This study examined the effect of linoleate, a member of the n-6 family, on regulation of the palmitate-induced inflammatory cytokine interleukin-8 (IL8) in hepatocytes. Palmitates 94-103 C-X-C motif chemokine ligand 8 Homo sapiens 134-147 24885871-3 2014 This study examined the effect of linoleate, a member of the n-6 family, on regulation of the palmitate-induced inflammatory cytokine interleukin-8 (IL8) in hepatocytes. Palmitates 94-103 C-X-C motif chemokine ligand 8 Homo sapiens 149-152 24885871-6 2014 RESULTS: Dose- and time-related changes of IL8 mRNA expression were examined and 9 h treatment with 500 muM palmitate showed the greatest elevation of IL8. Palmitates 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 24885871-6 2014 RESULTS: Dose- and time-related changes of IL8 mRNA expression were examined and 9 h treatment with 500 muM palmitate showed the greatest elevation of IL8. Palmitates 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 24885871-7 2014 Co-treatment with 500 muM palmitate and 400 muM linoleate significantly suppressed IL8 production below that with palmitate alone in both cells (both mRNA and protein). Palmitates 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 24885871-7 2014 Co-treatment with 500 muM palmitate and 400 muM linoleate significantly suppressed IL8 production below that with palmitate alone in both cells (both mRNA and protein). Linoleic Acid 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 24885871-7 2014 Co-treatment with 500 muM palmitate and 400 muM linoleate significantly suppressed IL8 production below that with palmitate alone in both cells (both mRNA and protein). Palmitates 114-123 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 24885871-10 2014 Treatment with 400 muM linoleate alone led to IL8 production (5.48 fold change), similar to co-treatment, with no influence on the expression of pJNK/IkBalpha. Linoleic Acid 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 24885871-12 2014 CONCLUSIONS: Linoleate is a potent regulator of the proinflammatory cytokine IL8 via the JNK and nuclear factor kappa B pathways that are involved in the pathophysiology of NASH, suggesting a future recommendation of dietary management. Linoleic Acid 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 24788721-9 2014 Immuno-suppressive effects of ZEA were further revealed through the suppression of lipopolysaccharide (LPS)-induced expression of pro-inflammatory cytokines (IL-6, IL-8 and IL-1beta). Zearalenone 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 24810615-8 2014 Following PZQ treatment there was an increase in the number of participants producing detectable levels of GST-specific cytokines (TNFalpha, IL-6, IL-8, IFNgamma, IL-12p70, IL-13 and IL-23p19) and also a shift in the GST-specific cytokine response towards a more pro-inflammatory phenotype than that observed before treatment. Praziquantel 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 24806487-5 2014 Via this process we identified three distinct chemical series, xanthines (SB711), quinazolininones (GSK223) and aminobenzothiazoles (GSK966) that selectively inhibited iE-DAP-stimulated IL-8 release via the NOD1 signaling pathway. Xanthines 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 24806487-5 2014 Via this process we identified three distinct chemical series, xanthines (SB711), quinazolininones (GSK223) and aminobenzothiazoles (GSK966) that selectively inhibited iE-DAP-stimulated IL-8 release via the NOD1 signaling pathway. sb711 74-79 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 24806487-5 2014 Via this process we identified three distinct chemical series, xanthines (SB711), quinazolininones (GSK223) and aminobenzothiazoles (GSK966) that selectively inhibited iE-DAP-stimulated IL-8 release via the NOD1 signaling pathway. quinazolininones 82-98 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 24806487-5 2014 Via this process we identified three distinct chemical series, xanthines (SB711), quinazolininones (GSK223) and aminobenzothiazoles (GSK966) that selectively inhibited iE-DAP-stimulated IL-8 release via the NOD1 signaling pathway. GSK223 100-106 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 24806487-5 2014 Via this process we identified three distinct chemical series, xanthines (SB711), quinazolininones (GSK223) and aminobenzothiazoles (GSK966) that selectively inhibited iE-DAP-stimulated IL-8 release via the NOD1 signaling pathway. aminobenzothiazoles 112-131 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 24806487-5 2014 Via this process we identified three distinct chemical series, xanthines (SB711), quinazolininones (GSK223) and aminobenzothiazoles (GSK966) that selectively inhibited iE-DAP-stimulated IL-8 release via the NOD1 signaling pathway. Diaminopimelic Acid 171-174 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 25306677-12 2014 There were no significant differences found in the levels of IL-6 and CRP between RIPC and control groups during the whole study Unexpectedly significant excess concentrations of IL-8 at 24 h were found when RIPC applied during sevoflurane anesthesia: 12.3 (10.6, 14.4) pg/mL in RIPCsevo group vs 6.2 (4.8, 11.1) pg/ml in CONTROLsevo group (p = 0.02). Sevoflurane 228-239 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 24474597-1 2014 OBJECTIVE: This study investigates whether early dynamic positron emission tomography/computed tomography (edPET/CT) using (18)F-sodium fluoride-((18)F-NaF) is feasible in depicting early phases of radiotracer distribution in patients with chronic osteomyelitis (COM). Sodium Fluoride 129-144 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 24631175-0 2014 Increased plasma glucose levels after change of recommendation from NaF to citrate blood collection tubes. Glucose 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 24631175-5 2014 CONCLUSIONS: The change from NaF to citrate tubes caused higher glucose values, and consequently more glucose determinations above the decision limit for diabetes. Citric Acid 36-43 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 24631175-5 2014 CONCLUSIONS: The change from NaF to citrate tubes caused higher glucose values, and consequently more glucose determinations above the decision limit for diabetes. Glucose 64-71 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 24631175-5 2014 CONCLUSIONS: The change from NaF to citrate tubes caused higher glucose values, and consequently more glucose determinations above the decision limit for diabetes. Glucose 102-109 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 24493202-8 2014 Fetuin-A upregulated IL-6 and IL-8, and this was potentiated by palmitate and blocked by CLI-095. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 24413578-12 2014 In multivariate analysis, baseline cholesterol levels and cardiopulmonary bypass duration were significant and independent determinants of the 3-hour postcardiopulmonary bypass increase in concentrations of procalcitonin and interleukin-8, but not of interleukin-6. Cholesterol 35-46 C-X-C motif chemokine ligand 8 Homo sapiens 225-238 25097896-1 2014 Our aim was to establish an easy and convenient procedure for the preparation of fluorine-18-sodium fluoride ((18)F-NaF) for bone positron emission tomography (PET) during routine (18)F-FDG production using the Explora FDG4 radiochemistry module (EFRM) by single run of Cyclotron with negligible radiation exposure. fluorine-18-sodium fluoride 81-108 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 24581581-10 2014 In marginal structural models, IL-1beta, IL-6, IL-8 were associated with lower estradiol and progesterone concentrations. Estradiol 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 24581581-10 2014 In marginal structural models, IL-1beta, IL-6, IL-8 were associated with lower estradiol and progesterone concentrations. Progesterone 93-105 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 24413629-1 2014 OBJECTIVE: To investigate whether glutamine deprivation induces expression of inflammatory cytokine interleukin-8 (IL-8) by determining NF-kappaB activity and levels of oxidative indices (ROS, reactive oxygen species; hydrogen peroxide; GSH, glutathione) in fibroblasts isolated from patients with ataxia telangiectasia (A-T). Glutamine 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 24413629-0 2014 Glutamine deprivation induces interleukin-8 expression in ataxia telangiectasia fibroblasts. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 25097896-1 2014 Our aim was to establish an easy and convenient procedure for the preparation of fluorine-18-sodium fluoride ((18)F-NaF) for bone positron emission tomography (PET) during routine (18)F-FDG production using the Explora FDG4 radiochemistry module (EFRM) by single run of Cyclotron with negligible radiation exposure. Fluorodeoxyglucose F18 186-189 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 24413629-1 2014 OBJECTIVE: To investigate whether glutamine deprivation induces expression of inflammatory cytokine interleukin-8 (IL-8) by determining NF-kappaB activity and levels of oxidative indices (ROS, reactive oxygen species; hydrogen peroxide; GSH, glutathione) in fibroblasts isolated from patients with ataxia telangiectasia (A-T). Glutamine 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 24413629-9 2014 RESULTS: While glutamine deprivation induced IL-8 expression and increased NF-kappaB DNA-binding activity in Mock cells, both processes were decreased by treatment of cells with glutamine or GSH or both glutamine and GSH. Glutamine 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 24413629-9 2014 RESULTS: While glutamine deprivation induced IL-8 expression and increased NF-kappaB DNA-binding activity in Mock cells, both processes were decreased by treatment of cells with glutamine or GSH or both glutamine and GSH. Glutamine 178-187 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 25097896-13 2014 The level of Kryptofix-222 (K222) in (18)F-NaF was within the prescribed limit. cryptating agent 222 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 24413629-9 2014 RESULTS: While glutamine deprivation induced IL-8 expression and increased NF-kappaB DNA-binding activity in Mock cells, both processes were decreased by treatment of cells with glutamine or GSH or both glutamine and GSH. Glutathione 191-194 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 24413629-9 2014 RESULTS: While glutamine deprivation induced IL-8 expression and increased NF-kappaB DNA-binding activity in Mock cells, both processes were decreased by treatment of cells with glutamine or GSH or both glutamine and GSH. Glutamine 178-187 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 24413629-14 2014 MEFs transfected with ATM siRNA and cultured without glutamine showed higher levels of ROS and IL-8 than those transfected with negative control siRNA; increased levels of ROS and IL-8 were suppressed by the treatment of glutamine. Glutamine 53-62 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 24413629-14 2014 MEFs transfected with ATM siRNA and cultured without glutamine showed higher levels of ROS and IL-8 than those transfected with negative control siRNA; increased levels of ROS and IL-8 were suppressed by the treatment of glutamine. Glutamine 221-230 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 25097896-13 2014 The level of Kryptofix-222 (K222) in (18)F-NaF was within the prescribed limit. cryptating agent 222 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 24413629-14 2014 MEFs transfected with ATM siRNA and cultured without glutamine showed higher levels of ROS and IL-8 than those transfected with negative control siRNA; increased levels of ROS and IL-8 were suppressed by the treatment of glutamine. Glutamine 221-230 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 24413629-15 2014 CONCLUSION: Glutamine deprivation induces ROS production, NF-kappaB activation, and IL-8 expression as well as a reduction in GSH in A-T fibroblasts, all of which are attenuated by glutamine supplementation. Glutamine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 24759736-9 2014 RESULT: H2O2 enhanced IL1beta-induced IL-6 and CXCL8 expression in NHBE and BEAS-2B cells whereas H2O2 alone did not have any affect. Hydrogen Peroxide 8-12 C-X-C motif chemokine ligand 8 Homo sapiens 47-52 24413629-15 2014 CONCLUSION: Glutamine deprivation induces ROS production, NF-kappaB activation, and IL-8 expression as well as a reduction in GSH in A-T fibroblasts, all of which are attenuated by glutamine supplementation. Glutamine 181-190 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 24589569-5 2014 TET significantly inhibited the induction of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 by phorbol 12-myristate 13-acetate (PMA) plus A23187. tetrandrine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 24589569-5 2014 TET significantly inhibited the induction of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 by phorbol 12-myristate 13-acetate (PMA) plus A23187. Tetradecanoylphorbol Acetate 143-174 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 24589569-5 2014 TET significantly inhibited the induction of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 by phorbol 12-myristate 13-acetate (PMA) plus A23187. Tetradecanoylphorbol Acetate 176-179 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 24589569-9 2014 Furthermore, TET suppressed the expression of TNF-alpha, IL-8, IL-6 and COX-2 through suppression of the ERK1/2, JNK1/2, IkappaBalpha degradation and phosphorylation, and NF-kappaB activation. tetrandrine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 24582799-8 2014 RESULTS: Repeated-measures three-way ANOVA (p=0.009) and Tukey"s test showed that CaL pre-rinse followed by NaF rinse significantly decreased surface loss of enamel when performed prior to an erosive challenge in comparison with the condition in which NaF only was used. calcium lactate 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 252-255 24582799-9 2014 CONCLUSIONS: Pre-rinse with CaL may increase the protection exerted by NaF against erosive wear. calcium lactate 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 24734646-0 2014 Upconversion luminescence properties of Yb3+ and Tm3+ codoped amorphous fluoride ZrF4-BaF2-LaF3-AlF3-NaF thin film prepared by pulsed laser deposition. Fluorides 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 25098981-0 2014 Assessment of serum interleukin-8 as a sensitive serological marker in monitoring the therapeutic effect of levamisole in recurrent aphthous ulcers: a randomized control study. Levamisole 108-118 C-X-C motif chemokine ligand 8 Homo sapiens 20-33 25098981-1 2014 AIM: The study was designed to evaluate the serum interleukin-8 (IL-8) levels in patients with recurrent aphthous ulcer (RAU) and monitor the immunomodulation and altered IL-8 levels by levamisole before therapy and after levamisole therapy. Levamisole 186-196 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 25098981-8 2014 Highly significant comparisons were obtained in the serum IL-8 between study and control groups before the onset of levamisole (t = 6.53, P <= 0.001). Levamisole 116-126 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 25098981-9 2014 IL-8 levels reduced by 72% after levamisole was instituted in RAU patients and comparison was highly significant for before and after levamisole onset (t = 5.54, P <= 0.001). Levamisole 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 25098981-9 2014 IL-8 levels reduced by 72% after levamisole was instituted in RAU patients and comparison was highly significant for before and after levamisole onset (t = 5.54, P <= 0.001). Levamisole 134-144 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24369896-4 2014 Metal concentrations were measured in sputum supernatant by inductively-coupled plasma mass spectrometry and correlated with sputum inflammatory cell counts, lactate dehydrogenase (LDH) and interleukin (IL)-8 concentrations, atmospheric particulate matter, lung function, clinical status and participant demographics. Metals 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 190-208 24369896-7 2014 The concentrations of magnesium, iron and zinc positively correlated with IL-8. Magnesium 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24369896-7 2014 The concentrations of magnesium, iron and zinc positively correlated with IL-8. Iron 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24964617-6 2014 RESULTS: The section of the IL-6, TNF-alpha, IL-1beta and IL-8 were the highest when THP-1 cells were exposed to NiSO4, DNCB and K2Cr2O7 for 6h, PPDA and TDI for 12h. nickel sulfate 113-118 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 24964617-6 2014 RESULTS: The section of the IL-6, TNF-alpha, IL-1beta and IL-8 were the highest when THP-1 cells were exposed to NiSO4, DNCB and K2Cr2O7 for 6h, PPDA and TDI for 12h. Dinitrochlorobenzene 120-124 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 24964617-6 2014 RESULTS: The section of the IL-6, TNF-alpha, IL-1beta and IL-8 were the highest when THP-1 cells were exposed to NiSO4, DNCB and K2Cr2O7 for 6h, PPDA and TDI for 12h. 4-(2'-pyridyldithio)benzyldiazoacetate 145-149 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 24964617-6 2014 RESULTS: The section of the IL-6, TNF-alpha, IL-1beta and IL-8 were the highest when THP-1 cells were exposed to NiSO4, DNCB and K2Cr2O7 for 6h, PPDA and TDI for 12h. Toluene 2,4-Diisocyanate 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 24554449-0 2014 Transcriptional and posttranscriptional regulation and endocytosis were involved in zinc oxide nanoparticle-induced interleukin-8 overexpression in human bronchial epithelial cells. Zinc Oxide 84-94 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 24743821-8 2014 Compared with normal cells, the NOD1 and NOD2 agonists, DAP and MDP, successfully increased IL-8 expression respectively (P<0.05). alpha,beta-diacryloxypropionic acid 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 24743449-6 2014 Since the Epidermal Growth Factor Receptor (EGFR) and reactive oxygen species (ROS) have been implicated in IL-8 release in response to activation of other G protein-coupled receptors, we examined their importance in S1P induced IL-8 release and established that they are not involved. Reactive Oxygen Species 54-77 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 24743449-6 2014 Since the Epidermal Growth Factor Receptor (EGFR) and reactive oxygen species (ROS) have been implicated in IL-8 release in response to activation of other G protein-coupled receptors, we examined their importance in S1P induced IL-8 release and established that they are not involved. Reactive Oxygen Species 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 24824707-0 2014 gamma-Globulin fraction proteins and their metal complexes with copper cations in induction of IL-8 production. Metals 43-48 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 24824707-0 2014 gamma-Globulin fraction proteins and their metal complexes with copper cations in induction of IL-8 production. Copper 64-70 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 24824707-1 2014 Plasma gamma-globulin fraction proteins, copper cations, and metal complexes formed by copper cations with human serum gamma-globulin induce the production of up to 4.0 ng/ml IL-8 by human blood cells. Copper 41-47 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 24824707-1 2014 Plasma gamma-globulin fraction proteins, copper cations, and metal complexes formed by copper cations with human serum gamma-globulin induce the production of up to 4.0 ng/ml IL-8 by human blood cells. Metals 61-66 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 24824707-1 2014 Plasma gamma-globulin fraction proteins, copper cations, and metal complexes formed by copper cations with human serum gamma-globulin induce the production of up to 4.0 ng/ml IL-8 by human blood cells. Copper 87-93 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 24743449-0 2014 Sphingosine 1-phosphate (S1P) induced interleukin-8 (IL-8) release is mediated by S1P receptor 2 and nuclear factor kappaB in BEAS-2B cells. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 24743449-0 2014 Sphingosine 1-phosphate (S1P) induced interleukin-8 (IL-8) release is mediated by S1P receptor 2 and nuclear factor kappaB in BEAS-2B cells. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 24743449-0 2014 Sphingosine 1-phosphate (S1P) induced interleukin-8 (IL-8) release is mediated by S1P receptor 2 and nuclear factor kappaB in BEAS-2B cells. sphingosine 1-phosphate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 24743449-0 2014 Sphingosine 1-phosphate (S1P) induced interleukin-8 (IL-8) release is mediated by S1P receptor 2 and nuclear factor kappaB in BEAS-2B cells. sphingosine 1-phosphate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 24743449-2 2014 Sphingosine 1-phosphate (S1P) is a bioactive lipid, increased in the airways of asthmatics, that may trigger the release of the potent neutrophil chemoattractant Interleukin-8 (IL-8) by epithelial cells. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 24743449-2 2014 Sphingosine 1-phosphate (S1P) is a bioactive lipid, increased in the airways of asthmatics, that may trigger the release of the potent neutrophil chemoattractant Interleukin-8 (IL-8) by epithelial cells. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 24743449-2 2014 Sphingosine 1-phosphate (S1P) is a bioactive lipid, increased in the airways of asthmatics, that may trigger the release of the potent neutrophil chemoattractant Interleukin-8 (IL-8) by epithelial cells. sphingosine 1-phosphate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 24743449-2 2014 Sphingosine 1-phosphate (S1P) is a bioactive lipid, increased in the airways of asthmatics, that may trigger the release of the potent neutrophil chemoattractant Interleukin-8 (IL-8) by epithelial cells. sphingosine 1-phosphate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 24782870-8 2014 STBM derived from preeclamptic placentas up-regulated the cell surface expression of CD54, and stimulated the secretion of the pro-inflammatory interleukin (IL)-6 and IL-8 in a similar, dose-dependent manner as did STBM prepared from normal placentas. stbm 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 24548972-9 2014 Additionally, the proposed hypothesis is strengthened by the indirect experimental findings indicating that CNTs and fullerenes induce an excessive expression of specific cytokines and chemokines (i.e. IL-8 and MCP1). Fullerenes 117-127 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 24705919-9 2014 IP-10 release was blocked by a PI3K inhibitor and IL-8 by dexamethasone. Dexamethasone 58-71 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 24705928-5 2014 A multi-steps binding mode is proposed: (i) the N-loop of CXCL-8 initially binds to the N-terminal domain of receptor CXCR1 driven predominantly by electrostatic interactions; (ii) hydrophobic interactions allow the N-terminal Glu-Leu-Arg (ELR) motif of CXCL-8 to move closer to the extracellular loops of CXCR1; (iii) electrostatic interactions finally dominate the interaction between the N-terminal ELR motif of CXCL-8 and the EC-loops of CXCR1. Glutamic Acid 227-230 C-X-C motif chemokine ligand 8 Homo sapiens 58-64 24705928-5 2014 A multi-steps binding mode is proposed: (i) the N-loop of CXCL-8 initially binds to the N-terminal domain of receptor CXCR1 driven predominantly by electrostatic interactions; (ii) hydrophobic interactions allow the N-terminal Glu-Leu-Arg (ELR) motif of CXCL-8 to move closer to the extracellular loops of CXCR1; (iii) electrostatic interactions finally dominate the interaction between the N-terminal ELR motif of CXCL-8 and the EC-loops of CXCR1. leucylarginine 231-238 C-X-C motif chemokine ligand 8 Homo sapiens 58-64 24694877-10 2014 In addition, embelin inhibited the expression of markers of angiogenesis (COX-2, VEGF, VEGFR, and IL-8), and metastasis (MMP-2 and MMP-9) in tumor tissues. embelin 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 23856970-5 2014 Ambroxol (100 nM) reduced RV14 titers and cytokine concentrations of interleukin (IL)-1beta, IL-6 and IL-8 in the supernatants and RV14 RNA in the cells after RV14 infection, in addition to reducing susceptibility to RV14 infection. Ambroxol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 24479526-7 2014 IL-33 increased ERK 1/2 phosphorylation in goblet cells (P < 0.05), and PD98059, a MAPK/ERK kinase inhibitor, attenuated IL-33-stimulated CXCL8/IL-8 secretion from goblet cells (P < 0.001). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 141-146 24554449-1 2014 Inhaled zinc oxide nanoparticles (ZnO-NPs) can induce lung inflammation through released inflammatory mediators, such as interleukin 8 (IL-8), from airways. Zinc Oxide 8-18 C-X-C motif chemokine ligand 8 Homo sapiens 121-134 24479526-7 2014 IL-33 increased ERK 1/2 phosphorylation in goblet cells (P < 0.05), and PD98059, a MAPK/ERK kinase inhibitor, attenuated IL-33-stimulated CXCL8/IL-8 secretion from goblet cells (P < 0.001). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 24554449-1 2014 Inhaled zinc oxide nanoparticles (ZnO-NPs) can induce lung inflammation through released inflammatory mediators, such as interleukin 8 (IL-8), from airways. Zinc Oxide 8-18 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 24554449-4 2014 The effect of ZnO-NPs on IL-8 mRNA stability was examined using mRNA decay assay. Zinc Oxide 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 24554449-5 2014 The phagocytosis inhibitor cytochalasin B (CB) was utilized to define the role of endocytosis in ZnO-NP-induced IL-8 expression. zno-np 97-103 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 24554449-7 2014 Exposure to ZnO-NPs significantly increased the expression of IL-8 mRNA and protein in a dose-dependent manner. Zinc Oxide 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 24554449-8 2014 Pretreatment with Act D blocked ZnO-NP-induced IL-8 expression. zno-np 32-38 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 24554449-9 2014 Both NFkappaB and C/EBPbeta transcription factors were required for ZnO-NP-induced IL-8 transcription. zno-np 68-74 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 24554449-10 2014 mRNA decay assay showed that ZnO-NP stimulation delayed IL-8 mRNA degradation in BEAS-2B cells. zno-np 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 24554449-11 2014 Pretreatment of BEAS-2B cells with CB blocked ZnO-NP-induced IL-8 expression by 30 %. zno-np 46-52 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 24554449-12 2014 Exposure to ZnO-NPs induced IL-8 gene expression through transcriptional activation and mRNA stabilization. Zinc Oxide 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 24554449-13 2014 Internalization of nanoparticles was partially involved in ZnO-NP-induced IL-8 expression. zno-np 59-65 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24226202-9 2014 Furthermore, both gene knockdown and pharmacological inhibition studies showed that COX-2 mediates the TNF-alpha/IL-8 pathway by increasing the production of prostaglandin E2 (PGE2). Dinoprostone 158-174 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 24521260-5 2014 After treatment of normal human epidermal keratinocytes with TCDD or PCBs, IL-6 and IL-8 production were increased. Polychlorinated Dibenzodioxins 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 24521260-5 2014 After treatment of normal human epidermal keratinocytes with TCDD or PCBs, IL-6 and IL-8 production were increased. Polychlorinated Biphenyls 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 24578240-1 2014 UNLABELLED: Under Medicare"s Coverage with Evidence Development policy, PET using (18)F-sodium fluoride (NaF PET) to identify osseous metastasis became a covered service if prospective registry data were collected. Sodium Fluoride 88-103 C-X-C motif chemokine ligand 8 Homo sapiens 105-108 24504098-4 2014 Accordingly, aganirsen inhibited (P < 0.001) in vitro the expression of interleukin-8 (IL-8), IL-12, IL-22, and tumor necrosis factor alpha (TNFalpha), four inflammatory mediators containing mRNA with AU-rich regions. GS 101 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 75-88 24504098-4 2014 Accordingly, aganirsen inhibited (P < 0.001) in vitro the expression of interleukin-8 (IL-8), IL-12, IL-22, and tumor necrosis factor alpha (TNFalpha), four inflammatory mediators containing mRNA with AU-rich regions. GS 101 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 24399465-0 2014 Thymoquinone suppression of the human hepatocellular carcinoma cell growth involves inhibition of IL-8 expression, elevated levels of TRAIL receptors, oxidative stress and apoptosis. thymoquinone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 24399465-6 2014 TQ treatments inhibited expression of NF-kappaB and suppressed IL-8 and its receptors. thymoquinone 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 24399465-10 2014 TQ enhanced TRAIL-induced death of HepG2 cells, in part by up-regulating TRAIL death receptors, inhibiting NF-kappaB and IL-8 and stimulating apoptosis. thymoquinone 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 24622069-5 2014 The influence of zerumbone on the angiogenic factors vascular endothelial growth factor and interleukin 8 was measured using the reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assays. zerumbone 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 24486342-7 2014 Additionally, using a ROS scavenger, a siRNA that targets AMPK, and various pharmacological inhibitors, we identified the signaling cascade that leads to induction of IL-8 by CSE. Reactive Oxygen Species 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 24486342-9 2014 Our findings suggest a novel role for glucosamine in alleviating the oxidative stress and lung inflammation induced by chronic CS exposure in vivo and in suppressing the CSE-induced IL-8 in vitro by inhibiting both the ROS-sensitive NADPH oxidase/AMPK/MAPK signaling pathway and the downstream transcriptional factors NF-kappaB and STAT3. Glucosamine 38-49 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 24999851-5 2014 METHODS: Metal concentrations were analyzed in three hydrofluorosilicic acid (HFS) and four sodium fluoride (NaF) samples using inductively coupled plasma-atomic emission spectrometry. Metals 9-14 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 24999851-8 2014 Two NaF samples contained barium (13 3-18 0 ppm) instead. Barium 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 24999851-9 2014 All HFS (212-415 ppm) and NaF (3312-3630 ppm) additives contained a surprising amount of aluminum. Aluminum 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 24446657-5 2014 When activated by TSH, they produce IL-6, IL-8, and TNF-alpha. Thyrotropin 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 25245457-2 2014 We show here that low extracellular magnesium stimulates the secretion of interleukin 8 and monocyte chemoattractant protein-1 in dermal microvascular endothelial cells. Magnesium 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 24338998-6 2014 Additionally, phloretin inhibited monocyte secretion of MCP-1, IL-6 and IL-8 responsible for pro-inflammatory activity of thrombin inducing endothelial CD40. Phloretin 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 24226202-9 2014 Furthermore, both gene knockdown and pharmacological inhibition studies showed that COX-2 mediates the TNF-alpha/IL-8 pathway by increasing the production of prostaglandin E2 (PGE2). Dinoprostone 176-180 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 24721407-5 2014 RESULTS: The inhibition ratio of IL-8 in the EM group was significantly higher than that in the CSE group, but lower than that in the control group (P<0.05). Erythromycin 45-47 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 24676135-7 2014 Moreover, cellular cytokines IL-1beta, IL-6, IL-8 and TNF-alpha secretion as well as NF-kappaB activation in THP-1 cells were attenuated under high iron conditions. Iron 148-152 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 24676135-8 2014 Low iron conditions in pure culture increased Salmonella invasion correlating with an increase in IL-8 release. Iron 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 24664110-0 2014 The pneumococcal polysaccharide capsule and pneumolysin differentially affect CXCL8 and IL-6 release from cells of the upper and lower respiratory tract. Polysaccharides 17-31 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 24647471-0 2014 Sphingosine 1-phosphate induces neutrophil chemoattractant IL-8: repression by steroids. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 24500711-3 2014 Although dexamethasone-mediated activation of the glucocorticoid receptor (GR) potently repressed expression of IL1beta, IL8, and several other pro-inflammatory TNF targets, the expression of anti-inflammatory TNF targets such as TNFAIP3 (A20) and NFKBIA was selectively spared or augmented by dexamethasone treatment. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 121-124 24528133-7 2014 Both ethanol and ethyl acetate extracts provided antiadhesion of H. pylori to AGS cells and down-regulation on the CagA, IL-8, COX-2, and iNOS expressions. ethyl acetate 17-30 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 24528133-7 2014 Both ethanol and ethyl acetate extracts provided antiadhesion of H. pylori to AGS cells and down-regulation on the CagA, IL-8, COX-2, and iNOS expressions. Ethanol 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 24647589-7 2014 Fetal brains were collected after 6 h. In human fetal membranes, silibinin significantly decreased LPS-stimulated expression of IL-6 and IL-8, COX-2, and prostaglandins PGE2 and PGF2alpha. Silybin 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 24647471-0 2014 Sphingosine 1-phosphate induces neutrophil chemoattractant IL-8: repression by steroids. Steroids 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 24647589-9 2014 Preterm fetal membranes with active infection treated with silibinin showed a decrease in IL-6, IL-8 and MMP-9 expression. Silybin 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 24647471-6 2014 The corticosteroid dexamethasone significantly represses IL-8 mRNA expression and protein secretion in a concentration- and time-dependent manner. Dexamethasone 19-32 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 24629040-8 2014 Treatments with PI3K inhibitors, Erk1/2 inhibitor, or Erlotinib significantly inhibited BTC-induced CXCL8 production and cell proliferation and movement. Erlotinib Hydrochloride 54-63 C-X-C motif chemokine ligand 8 Homo sapiens 100-105 24499049-4 2014 Ni(II)-NTA-DG and the formed polyplexes induced an activation of iDCs, showing an increasing expression of costimulatory molecules CD86, CD80, and proinflammatory cytokines IL-6 and IL-8. ni(ii)-nta-dg 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 24669186-8 2014 RESULTS: Genistein decreased the secretion of IL-1beta, IL-6, and IL-8 from TNF-alpha-stimulated MH7A cells in a dose-dependent manner. Genistein 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 24669186-10 2014 The production of IL-1beta, IL-6, and IL-8 induced by TNF-alpha was decreased by the phosphatidylinositol-3 kinase inhibitor LY294002, suggesting that inhibition of Akt activation might inhibit IL-1beta, IL-6, and IL-8 production induced by TNF-alpha. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 24669186-10 2014 The production of IL-1beta, IL-6, and IL-8 induced by TNF-alpha was decreased by the phosphatidylinositol-3 kinase inhibitor LY294002, suggesting that inhibition of Akt activation might inhibit IL-1beta, IL-6, and IL-8 production induced by TNF-alpha. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 24629144-0 2014 Simvastatin down-regulates the production of interleukin-8 by neutrophil leukocytes from dyslipidemic patients. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 24629144-2 2014 Aim of the study is to investigate the production of IL-8 by PMN leukocytes from dyslipidemic patients treated with simvastatin. Simvastatin 116-127 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 24629144-6 2014 Moreover, the fMLP-induced IL-8 production in dyslipidemic untreated patients was higher than that of controls (p < 0.05) and was reduced after simvastatin treatment (p < 0.01). Simvastatin 147-158 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 24629144-8 2014 CONCLUSIONS: Prolonged treatment with simvastatin is associated with a reduction of IL-8 production, suggesting the possibility of statin to modulate the pro-inflammatory response in PMNs of patients with moderately increased cardiovascular risk. Simvastatin 38-49 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 23625984-10 2014 Dexamethasone downregulated pro-inflammatory mediator (IL-1beta, IL-6, TNFalpha, IFNgamma, MMP-9, TIMP-1, CCL3 and CXCL8) mRNAs but did not modify expression of vascular remodelling factors (platelet derived growth factor, MMP-2 and collagens I and III). Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 115-120 24598028-4 2014 RESULTS: Using RasG12V that recapitulates multiple stimulations induced by receptor tyrosine kinases, we found that RasG12V alone induced CXCL8 expression at the mRNA and protein levels, whereas down-regulation of p53 did not. rasg12v 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 138-143 24717945-5 2014 The epidermal growth factor receptor tyrosine kinase inhibitor AG1478 inhibited the coculture-induced secretion of MUC5AC, PDGF-AB, VEGF, and IL-8. RTKI cpd 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24354854-0 2014 A novel phenylcyclohex-1-enecarbothioamide derivative inhibits CXCL8-mediated chemotaxis through selective regulation of CXCR2-mediated signalling. phenylcyclohex-1-enecarbothioamide 8-42 C-X-C motif chemokine ligand 8 Homo sapiens 63-68 24310318-6 2014 Dapsone has been investigated predominantly by in vitro methods aiming to get more insights into the effect of dapsone to inflammatory effector cells, cytokines, and/or mediators, such as cellular toxic oxygen metabolism, myoloperoxidase-/halogenid system, adhesion molecules, chemotaxis, membrane-associated phospholipids, prostaglandins, leukotrienes, interleukin-8, tumor necrosis factor alpha, lymphocyte functions, and tumor growth. Dapsone 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 354-396 24581246-8 2014 Acrolein was pro-inflammatory for the PNEC cultures (30 muM exposure for 4 h inducing a 2.0 fold increase in IL-8 release) and also increased IL-8 release after stimulation with PA LPS. Acrolein 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 24581246-8 2014 Acrolein was pro-inflammatory for the PNEC cultures (30 muM exposure for 4 h inducing a 2.0 fold increase in IL-8 release) and also increased IL-8 release after stimulation with PA LPS. Acrolein 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24581246-8 2014 Acrolein was pro-inflammatory for the PNEC cultures (30 muM exposure for 4 h inducing a 2.0 fold increase in IL-8 release) and also increased IL-8 release after stimulation with PA LPS. Protactinium 178-180 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24581246-9 2014 In contrast, nicotine had anti-inflammatory properties (0.6 fold IL-8 release after 50 muM exposure to nicotine for 24 h), and acetylaldehyde was without effect. Nicotine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 24581246-9 2014 In contrast, nicotine had anti-inflammatory properties (0.6 fold IL-8 release after 50 muM exposure to nicotine for 24 h), and acetylaldehyde was without effect. Nicotine 103-111 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 24579814-4 2014 The associated half-maximal effective concentration (EC50) values for Gro-alpha and IL-8 of 8 and 22 pM, respectively, are between two and three orders of magnitude below the so-far reported EC50 values of these chemokines for the induction of neutrophilic calcium release, integrin expression, degranulation, and receptor internalization. Calcium 257-264 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 24579814-5 2014 Sch527123, a known inhibitor of CXCR2 (KD=49 pM) and with a lower potency/affinity also of CXCR1 (KD=3.9 nM), antagonized actin remodeling with half-maximal inhibitory concentration (IC50) values of 400 pM for the CXCR2-specific agonist Gro-alpha and of 36 nM for the CXCR1/2-promiscuous agonist IL-8. 2-hydroxy-N,N-dimethyl-3-(2-((1-(5-methylfuran-2-yl)propyl)amino)-3,4-dioxocyclobut-1-enylamino)benzamide 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 296-300 24837313-7 2014 Adenosine modified myeloid cells express also higher levels of mRNA of proinflammatory cytokines and chemoattractants (IL-6, IL-8, IL-1 b). Adenosine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 24508669-1 2014 BACKGROUND: 18F-Sodium fluoride (18F-NaF) and 18F-fluorodeoxyglucose (18F-FDG) are promising novel biomarkers of disease activity in aortic stenosis. 18f-sodium fluoride 12-31 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 24508669-7 2014 Baseline 18F-NaF uptake correlated closely with the change in calcium score (r=0.66; P<0.01), and this improved further (r=0.75; P<0.01) when 18F-NaF uptake overlying computed tomography-defined macrocalcification was excluded. Calcium 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 24463979-0 2014 Interleukin 8 inhibition enhanced cholesterol efflux in acetylated low-density lipoprotein-stimulated THP-1 macrophages. Cholesterol 34-45 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 24745085-5 2014 The addition of NaF as preservative improved the stability of opiates at all conditions studied, whereas the type of anticoagulant did not affect the stability of opiates. Opiate Alkaloids 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 24489105-4 2014 Serum levels of IFN-gamma, CCL4, and TNF-alpha were significantly increased, whereas CXCL8 significantly decreased from pretreatment (PRE) to early during treatment (EDT) serum samples. edt 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 85-90 24429901-4 2014 Of the controlled trials, the one including CRS patients just without polyps, showed a significant effect in sino-nasal outcome test, saccharine transit time, nasal endoscopy, and IL-8 levels in lavage fluid after 12 weeks of roxithromycin, whereas, in the other RCT with a mixed study group of CRS patients with and without polyps, 12 weeks of azithromycin showed no effect compared to placebo. Roxithromycin 226-239 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 24700927-8 2014 Moreover, in an in vitro model of psoriasis (RHE), Calcitriol significantly inhibited relevant gene expression of chemokines (Interleukin-8, Regulated upon Activation Normal T-cell Expressed and Secreted [RANTES]) and psoriasin (S100A7). Calcitriol 51-61 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 24571702-4 2014 RESULTS: Specimens treated with the Sn-containing NaF dentifrice showed 6.5 mum of surface loss +- 1.2 (SEM), which was not significantly different (P < 0.05, Fisher LSD) from that of a clinically proven, stabilised SnF2 positive control [Crest( ) Pro-Health, 1,100 ppm F as SnF2 : 3.0 mum of surface loss +- 1.1 (SEM)]. Tin 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 24641605-7 2014 On the other hand, IL-10 and IFN- alpha caused a significant decrease in type I collagen production, and IL-8 and GM-CSF caused a decrease in hyaluronan production compared with no cytokine-treated control. Hyaluronic Acid 142-152 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 24463979-9 2014 Taken together, our results indicate that IL-8 exerts negative regulatory effects on cholesterol efflux from THP-1 cells and may thus represent a potential target for prevention and treatment of atherosclerosis. Cholesterol 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 24489105-5 2014 The decrease in serum CXCL8 levels from PRE to EDT significantly correlated with decreases in markers of melanoma proliferation (Ki-67) and increases in cytotoxic tumor-infiltrating T cells in corresponding tumor biopsies. edt 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 22-27 24489105-6 2014 In addition, a greater fold reduction in CXCL8 serum levels from PRE to EDT serum samples was associated with decreased overall survival. edt 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 41-46 24463979-3 2014 However, the effect of IL-8 on cholesterol efflux is still unclear. Cholesterol 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 24463979-6 2014 Five and 10 microg/mL of human IL-8-neutralizing antibody enhanced cholesterol efflux from THP-1-derived macrophages by 1.2- and 1.4-fold, respectively. Cholesterol 67-78 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 24501198-4 2014 In this study, we have shown that TSG-6 inhibits chemokine-stimulated transendothelial migration of neutrophils via a direct interaction (KD, ~ 25 nM) between TSG-6 and the glycosaminoglycan binding site of CXCL8, which antagonizes the association of CXCL8 with heparin. Glycosaminoglycans 173-190 C-X-C motif chemokine ligand 8 Homo sapiens 207-212 24510965-9 2014 Overexpression of AGS3 in RBL-CXCR2 significantly inhibited CXCL8-induced Ca(2+) mobilization, phosphoinositide hydrolysis, and chemotaxis. Phosphatidylinositols 95-111 C-X-C motif chemokine ligand 8 Homo sapiens 60-65 24501198-4 2014 In this study, we have shown that TSG-6 inhibits chemokine-stimulated transendothelial migration of neutrophils via a direct interaction (KD, ~ 25 nM) between TSG-6 and the glycosaminoglycan binding site of CXCL8, which antagonizes the association of CXCL8 with heparin. Glycosaminoglycans 173-190 C-X-C motif chemokine ligand 8 Homo sapiens 251-256 24463979-8 2014 Ten micromoles of SB203580, an inhibitor of p38, almost completely suppressed the production of IL-8 from acetylated low-density lipoprotein-loaded THP-1 macrophages and accelerated cholesterol efflux. SB 203580 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 24501198-5 2014 Furthermore, we found that TSG-6 impairs the binding of CXCL8 to cell surface glycosaminoglycans and the transport of CXCL8 across an endothelial cell monolayer. Glycosaminoglycans 78-96 C-X-C motif chemokine ligand 8 Homo sapiens 56-61 24418375-3 2014 beta-glucan attenuated CD86 and CD80 expression and simultaneously reduced secretion of the inflammatory cytokines IL-2, IL-8, IL-12, TNF-alpha and IFN-gamma. beta-Glucans 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 24320086-8 2014 Resveratrol suppressed TNF-alpha-induced IL-8 release from the ESC in a dose-dependent manner while sirtinol increased IL-8 release. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 24320086-8 2014 Resveratrol suppressed TNF-alpha-induced IL-8 release from the ESC in a dose-dependent manner while sirtinol increased IL-8 release. sirtinol 100-108 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 24399488-6 2014 In addition, FME reduced the H2O2-induced expression of interleukin-8 at both the mRNA and protein levels in Caco-2 cells. Hydrogen Peroxide 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 24257482-1 2014 AIM: (18)F-Sodium fluoride ((18)F-NaF) PET/computed tomography (CT) has improved spatial resolution in the cervical spine compared with single photon emission computed tomography/CT techniques using traditional tracers. Sodium Fluoride 11-26 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 24418375-6 2014 In experiments with monocytes derived from healthy donors, beta-glucan inhibited IL-8, IL-12 and TNF-alpha production. beta-Glucans 59-70 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 24494989-2 2014 The highly reversible electrochemical reactivity of CFx with Na at room temperature indicates that the decomposition of NaF could be driven by carbon formed during the first discharge. Cefoxitin 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 24527095-8 2014 It was found that lipopolysaccharide and Pac significantly increase the secretion of IL-6 and IL-8 in the SKOV3 cell line. Paclitaxel 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 24527095-9 2014 Similarly, Pac resulted in a significant upregulation of IL-6 and IL-8 in OVCAR3 cells, but not in A2780 and 3AO cells. Paclitaxel 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 24587317-9 2014 In primary hPdLCs, both 25(OH)D3 and 1,25(OH)2D3 inhibited the production of IL-8 and MCP-1 but have no significant effect on the IL-6 production. Calcifediol 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 24587317-9 2014 In primary hPdLCs, both 25(OH)D3 and 1,25(OH)2D3 inhibited the production of IL-8 and MCP-1 but have no significant effect on the IL-6 production. Calcitriol 37-48 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 24494989-2 2014 The highly reversible electrochemical reactivity of CFx with Na at room temperature indicates that the decomposition of NaF could be driven by carbon formed during the first discharge. Carbon 143-149 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 24459103-3 2014 To improve this situation, BODIPY-amidothiourea dyes with varying hydrogen-bond donating strengths were developed, the most H-acidic of which (1 c) could detect F(-) from an inorganic source (NaF) in 50 % aqueous solution (DMSO/water 1:1, v/v) with 0.01 ppm sensitivity through selective fluorescence quenching by a photoinduced electron-transfer (PET) process. bodipy-amidothiourea 27-47 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 24555532-8 2014 IL-8 release was blocked by EGFR neutralizing antibodies, an EGFR-selective tyrosine kinase inhibitor and by the metalloprotease inhibitor, GM6001, which blocks EGFR ligand shedding. N-(2(R)-2-(hydroxamidocarbonylmethyl)-4-methylpentanoyl)-L-tryptophan methylamide 140-146 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24693448-2 2014 The chemical mediator prostaglandin E2 (PGE2) and cytokines such as interleukin- (IL-)6 and IL-8 have been known to play important roles in inflammatory responses and tissue degradation. Dinoprostone 22-38 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 24586752-4 2014 We found that the ceramide metabolite sphingosine-1-phosphate (S1P) stimulated the production of inflammatory mediators such as TNF-alpha and IL-8 from three-dimensionally cultured human primary keratinocytes (termed "3D keratinocytes"), which form a stratum corneum. Ceramides 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24586752-4 2014 We found that the ceramide metabolite sphingosine-1-phosphate (S1P) stimulated the production of inflammatory mediators such as TNF-alpha and IL-8 from three-dimensionally cultured human primary keratinocytes (termed "3D keratinocytes"), which form a stratum corneum. sphingosine 1-phosphate 38-61 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24586752-4 2014 We found that the ceramide metabolite sphingosine-1-phosphate (S1P) stimulated the production of inflammatory mediators such as TNF-alpha and IL-8 from three-dimensionally cultured human primary keratinocytes (termed "3D keratinocytes"), which form a stratum corneum. sphingosine 1-phosphate 63-66 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24586752-6 2014 In the presence of the detergent Triton X-100, which damages stratum corneum structure, PaCDase, but not heat-inactivated PaCDase or PaCDase-inactive mutant, induced the production of TNF-alpha, endothelin-1, and IL-8, indicating that this production was dependent on ceramidase activity. Octoxynol 33-45 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 24586752-7 2014 Among various ceramide metabolites, sphingosine and S1P enhanced the gene expression of TNF-alpha, endothelin-1, and IL-8. Ceramides 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 24586752-7 2014 Among various ceramide metabolites, sphingosine and S1P enhanced the gene expression of TNF-alpha, endothelin-1, and IL-8. Sphingosine 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 24586752-11 2014 The NF-kappaB inhibitor curcumin significantly inhibited PaCDase-induced expression of IL-8 and endothelin-1. Curcumin 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 24586752-13 2014 Collectively, these findings suggest that (i) 3D keratinocytes produce S1P from sphingosine, which is produced through the hydrolysis of ceramide by PaCDase, (ii) S1P induces the production of TNF-alpha via S1P receptors, and (iii) released TNF-alpha stimulates the production of inflammatory mediators such as IL-8. Sphingosine 80-91 C-X-C motif chemokine ligand 8 Homo sapiens 311-315 24459103-3 2014 To improve this situation, BODIPY-amidothiourea dyes with varying hydrogen-bond donating strengths were developed, the most H-acidic of which (1 c) could detect F(-) from an inorganic source (NaF) in 50 % aqueous solution (DMSO/water 1:1, v/v) with 0.01 ppm sensitivity through selective fluorescence quenching by a photoinduced electron-transfer (PET) process. Dimethyl Sulfoxide 223-227 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 24459103-3 2014 To improve this situation, BODIPY-amidothiourea dyes with varying hydrogen-bond donating strengths were developed, the most H-acidic of which (1 c) could detect F(-) from an inorganic source (NaF) in 50 % aqueous solution (DMSO/water 1:1, v/v) with 0.01 ppm sensitivity through selective fluorescence quenching by a photoinduced electron-transfer (PET) process. Water 228-233 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 24499192-0 2014 Pseudomonas pyocyanin stimulates IL-8 expression through MAPK and NF-kappaB pathways in differentiated U937 cells. Pyocyanine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 24499192-4 2014 RESULTS: It was found that PCN increased IL-8 release and mRNA expression in Phorbol 12-myristate 13-acetate (PMA) differentiated U937 cells in both a concentration- and time-dependent manner by reverse transcription-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA). Pyocyanine 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 24499192-4 2014 RESULTS: It was found that PCN increased IL-8 release and mRNA expression in Phorbol 12-myristate 13-acetate (PMA) differentiated U937 cells in both a concentration- and time-dependent manner by reverse transcription-polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA). Tetradecanoylphorbol Acetate 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 24499192-8 2014 The results were further confirmed by the observation that p38, ERK1/2 and NF-kappaB inhibitors inhibited PCN-induced NF-kappaB activation and attenuated PCN-induced IL-8 expression in U937 cells as a function of their concentrations. Pyocyanine 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 24499192-9 2014 Moreover, it was shown that PCN induced oxidative stress in U937 cells and N-acetyl cysteine, an antioxidant, was able to inhibit PCN-induced IL-8 protein expression. Pyocyanine 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24499192-9 2014 Moreover, it was shown that PCN induced oxidative stress in U937 cells and N-acetyl cysteine, an antioxidant, was able to inhibit PCN-induced IL-8 protein expression. Acetylcysteine 75-92 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24499192-9 2014 Moreover, it was shown that PCN induced oxidative stress in U937 cells and N-acetyl cysteine, an antioxidant, was able to inhibit PCN-induced IL-8 protein expression. Pyocyanine 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 24499192-10 2014 CONCLUSIONS: It is concluded that PCN induces IL-8 secretion and mRNA expression in PMA-differentiated U937 cells in a concentration- and time- dependent manner. Pyocyanine 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 24499192-11 2014 Furthermore, p38 and ERK MAPKs and NF-kappaBeta signaling pathways may be involved in the expression of IL-8 in PCN-incubated PMA-differentiated U937 cells. Pyocyanine 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 24284797-9 2014 Interestingly, treatment of HCT116 cells with a small interference RNA specifically targeting SRSF3-PTC mRNA significantly attenuated arsenite-stimulated induction of c-JUN protein, its binding activity to the AP-1 binding site (-126 to 120 bp) in the interleukin (IL)-8 gene promoter, and AP-1 promoter activity, resulting in significant reduction of arsenite-stimulated IL-8 production. arsenite 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 252-270 24211732-5 2014 Necrotic damage was most likely due to osmotic stress, and our results suggest that magnesium ion build-up is also involved in the interleukin 8 release. Magnesium 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 131-144 24284797-9 2014 Interestingly, treatment of HCT116 cells with a small interference RNA specifically targeting SRSF3-PTC mRNA significantly attenuated arsenite-stimulated induction of c-JUN protein, its binding activity to the AP-1 binding site (-126 to 120 bp) in the interleukin (IL)-8 gene promoter, and AP-1 promoter activity, resulting in significant reduction of arsenite-stimulated IL-8 production. arsenite 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 372-376 23931157-4 2014 The co-incubation of the cells with Ind, at a nutritionally relevant concentration (5-25 muM), and IL-1beta prevented the release of the pro-inflammatory cytokines IL-6 and IL-8, PGE2 and NO, the formation of ROS and the loss of thiols in a dose-dependent manner. indicaxanthin 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 24136171-5 2014 The selective cell-permeable inhibitor of PKC-beta and the broad PKC inhibitor GF109203X completely prevented chemical allergen- or lipopolysaccharide (LPS)-induced CD86 expression and significantly modulated IL-8 release (50 % reduction). bisindolylmaleimide I 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 23981542-10 2014 Resveratrol was superior to dexamethasone in reducing CCL-2, IL-6 and IL-8 in LTA-exposed HASMCs of patients with COPD. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 23981542-10 2014 Resveratrol was superior to dexamethasone in reducing CCL-2, IL-6 and IL-8 in LTA-exposed HASMCs of patients with COPD. hasmcs 90-96 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 24030221-7 2014 Furthermore, passive smoke exposure reduced the inhibitory effects of dexamethasone on tumor necrosis factor-alpha-induced CXCL8 release in AMs. Dexamethasone 70-83 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 24292270-6 2014 Twenty nanometers CPS particles stimulated IL-8 secretion in human monocytes and induced oxidative burst in monocytes. cps 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 24292270-7 2014 Five hundred nanometers and 1,000 nm CPS particles stimulated IL-6 and IL-8 secretion in monocytes and macrophages, chemotaxis towards a chemotactic stimulus of monocytes and phagocytosis of bacteria by macrophages and provoked an oxidative burst of granulocytes. cps 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 24372819-6 2014 Treatment of HaCaT cells with histamine and TNFalpha enhanced the mRNA expression of interleukin (IL)-8. Histamine 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 85-103 24502806-12 2014 In vitro assays revealed that TMP inhibited NF-kappaB translocation and its downstream production of inflammatory factors, such as TNF-alpha, IL-6 and IL-8, and that ROS production that was induced by LPS in Caco-2 cells. tetramethylpyrazine 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 24338213-4 2014 We find that these ions may be generated efficiently by two distinct methods: (1) negative ion ESI of a methanolic solution containing the fatty acid and sodium fluoride forming an [M - H + NaF](-) ion. Fatty Acids 139-149 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 24318613-0 2014 Divergent determinants of 18F-NaF uptake and visible calcium deposition in large arteries: relationship with Framingham risk score. Fluorine-18 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 24296811-9 2014 Pretreatment with an antioxidant suppressed TNFalpha-induced IL-8 expression, confirming the role of ROS in TNFalpha signaling. Reactive Oxygen Species 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 24338213-4 2014 We find that these ions may be generated efficiently by two distinct methods: (1) negative ion ESI of a methanolic solution containing the fatty acid and sodium fluoride forming an [M - H + NaF](-) ion. Sodium Fluoride 154-169 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 24377455-8 2014 Compared with placebo, the consumption of bayberry juice significantly decreased the plasma levels of protein carbonyl groups (P = 0.038), tumor necrosis factor-alpha (P < 0.001), and interleukin-8 (P = 0.022). bayberry juice 42-56 C-X-C motif chemokine ligand 8 Homo sapiens 187-200 24370750-2 2014 The observed linear-mode trajectory pattern of neutrophils toward N-formyl-methionyl-leucyl-phenylalanine (fMLP) or Interleukin (IL)-8/CXCL8 was distinguished from random migration patterns toward leukotriene (LT) B4 or platelet activating factor (PAF). Leukotrienes 197-208 C-X-C motif chemokine ligand 8 Homo sapiens 135-140 24268047-9 2014 EGF prompted the cell movement in both HepG2 and HCCLM3 and regulated the production of CXCL5 and CXCL8 from HCC, which were inhibited by EGFR inhibitor, Erk inhibitor (U0126), or PI3K inhibitors (BEZ-235 and SHBM1009). U 0126 169-174 C-X-C motif chemokine ligand 8 Homo sapiens 98-103 24316968-7 2014 Carnosol not only inhibited TNF-alpha-induced protein expression of intercellular adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1 and E-selectin in HUVECs, but also suppressed interleukin (IL)-8 and monocyte chemoattractant protein (MCP)-1 expression. carnosol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 197-215 24394883-12 2014 In response to exposure to lactobacilli EPSs HT29-19A cells produce significantly increased levels of the proinflammatory cytokine IL-8. epss 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 24269928-6 2014 Carbachol concentration-dependently enhanced the production of IL-1beta-induced IL-6 and IL-8, which was blocked by the simultaneous addition of tiotropium. Carbachol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 24269928-6 2014 Carbachol concentration-dependently enhanced the production of IL-1beta-induced IL-6 and IL-8, which was blocked by the simultaneous addition of tiotropium. Tiotropium Bromide 145-155 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 24269928-7 2014 The combination of olodaterol plus tiotropium further reduced IL-6 and IL-8 release. olodaterol 19-29 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 24731418-1 2014 OBJECTIVE: To compare the ability of the polysaccharide from various Porphyromonas gingivalis (Pg) type and clinical strains in inducing THP-1 cells to produce cytokines interleukin(IL)-1beta, IL-8, and tumor necrosis factor(TNF)-alpha, in order to analyze the immunogenicity of Pg polysaccharide components and the virulence-associated factors of this periodontal pathogen. Polysaccharides 41-55 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 24731418-8 2014 CONCLUSIONS: Polysaccharide extracted from Pg could induced the THP-1 cells to secrete the cytokines of IL-1beta, IL-8 and TNF-alpha. Polysaccharides 13-27 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 24396446-9 2014 The following parameters were found to be reduced following the use of methylprednisolone: Interleukin (IL)-6 immediately following surgery and on postoperative days (PODs) 1 and 3; IL-8 immediately following surgery; and PaO2/FiO2 on POD 3. Methylprednisolone 71-89 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 24337575-5 2014 The responsible mechanism involves an increased nuclear accumulation of IkappaB kinase beta (IKKbeta) and an increased recruitment of the nuclear IKKbeta, p65-phosphorylated at Ser-536, and the transcription factor early growth response-1 (EGR-1) to the endogenous IL-8 promoter. Serine 177-180 C-X-C motif chemokine ligand 8 Homo sapiens 265-269 24344116-8 2014 Modulation of genes related with invasion, metastasis and chemoresistance (ICAM-1, CXCL1, TNFAIP3, IL8) were confirmed in additional doxorubicin-treated cell lines and fresh primary human breast tumors. Doxorubicin 133-144 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 24551277-7 2014 HeLa and SiHa cells cultured in 1% oxygen showed the increased viability and apoptosis, and the former effect could be partly reversed by anti-human IL-8 neutralizing antibody. Oxygen 35-41 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 24485462-5 2014 Specifically, the nitrogen mustard cyclophosphamide induces an acute secretory activating phenotype (ASAP), releasing CCL4, IL8, VEGF, and TNFalpha from treated tumor cells. Nitrogen 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 24485462-5 2014 Specifically, the nitrogen mustard cyclophosphamide induces an acute secretory activating phenotype (ASAP), releasing CCL4, IL8, VEGF, and TNFalpha from treated tumor cells. Cyclophosphamide 35-51 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 24475177-6 2014 Vitamin D supplementation had no significant effects on RV replication, but potentiated secretion of CXCL8 and CXCL10 from infected or uninfected cells. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 24117378-4 2014 We demonstrated that girolline inhibits signaling through both MyD88-dependent and -independent TLRs (i.e., TLR2, 3, 4, 5, and 7) and reduces cytokine (IL-6 and IL-8) production in human peripheral blood mononuclear cells and macrophages. girolline 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 24231947-10 2014 CONCLUSION: IL8-level changes during pazopanib allowed for a prognostic improvement and were associated with response probability. pazopanib 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 24296301-10 2014 Solvent (DMSO) controls exhibited statistically significantly decreased responses compared with non-treated controls for IL-6 release and IL-8 mRNA expression, but these responses were not consistent across experiments and times. Dimethyl Sulfoxide 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 24401117-11 2014 Expression of the IL-8 data with respect to either of these metrics eliminated the differential response between the RTI amosite sample and the other samples that was observed when HAEC were exposed on an equal mass basis. Asbestos, Amosite 121-128 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 24129312-2 2014 In the current study, we generated and characterized a 2"-fluoro-pyrimidine modified RNA aptamer (8A-35) against human IL-8. 2"-fluoro-pyrimidine 55-75 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 25257149-4 2014 IL-8 production by HaCaT cells is stimulated by egg-oil whilst in phythemagglutin in-activated PBMLs production of the interleukins IL-2, IL-6, IL-10 and IFN-gamma and TFN-alpha is reduced. egg-oil 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24128422-2 2014 We investigated the effect of lipopolysacharide (LPS) and progesterone (P4) upon expression of TLR-4/MyD88, TNFalpha, IL-6, IL-8, IL-10, and HBD2 on the human amniotic epithelium. Progesterone 58-70 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 24128422-6 2014 LPS increased the concentrations of TNFalpha, IL-6, IL-8, IL-10, and HBD2 by factors of 30-, eight, three, three, and fivefold, respectively. lps 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 24164087-7 2014 Budesonide also reduced the concentrations of tumour necrosis factor-alpha, interleukin-1beta, interleukin-6 and interleukin-8 in bronchoalveolar lavage fluid, but increased interleukin-10 30 min after re-expansion (p < 0.05 for all measures). Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 25169512-0 2014 Influence of propofol, isoflurane and enflurance on levels of serum interleukin-8 and interleukin-10 in cancer patients. Propofol 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 25169512-1 2014 OBJECTIVE: To observe the influence of propofol, isoflurane and enflurance on interleukin-8 (IL-8) and IL-10 levels in cancer patients. Propofol 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 25169512-12 2014 CONCLUSIONS: Propofol, which is better in inhibiting serum IL-8 secretion and improving IL-10 secretion than isoflurane and enflurance, can be regarded as a preferable anesthetic agent in inhibiting traumatic inflammatory responses. Propofol 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 25147797-5 2014 Increases of IL-6 and IL-8 release (by ELISA) were detected in A549 cells exposed to MWCNTs-COOH from 10 mug/mL while IL-8 increased in BEAS-2B cells exposed to pristine MWCNTs at 20 and 40 mug/mL. Carbonic Acid 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 25162011-7 2014 RA produced a significant reduction in UVB-induced expression of IL-6, IL-8, MCP-1, and TNF-alpha when applied at the same time as irradiation. rosmarinic acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 25140317-9 2014 Furthermore, we found that doxorubicin resistance of TNBC was mediated by IL-8 presented in the MSC-secreted CM. Doxorubicin 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 25162011-3 2014 We assessed the ability of EA and RA to modulate IL-1beta, IL-6, IL-8, IL-10, MCP-1, and TNF-alpha gene expression in HaCaT cells after UVB irradiation. Ellagic Acid 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 25140722-0 2014 Insoluble NaF in Duraphat may prolong fluoride reactivity of varnish retained on dental surfaces. sodium fluoride topical preparation 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 25140722-8 2014 In conclusion, a longer varnish retention time than the usually recommended could improve the anticaries effect of Duraphat varnish, allowing that NaF particles, initially insoluble in the varnish matrix, prolong the reactivity with enamel. sodium fluoride topical preparation 115-123 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 24789288-1 2014 This study compared in situ the application of 4% titanium tetrafluoride (TiF4) solution and 2% sodium fluoride (NaF) gel on artificial white-spot lesions in human enamel. Sodium Fluoride 96-111 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 25430458-9 2014 A positive correlation was found between levels of serum SO2 and intracellular NF-kappaB/IL-8, and the correlation coefficients were 0.671 and 0.798 (P < 0.05), respectively. Sulfur Dioxide 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 24220935-6 2014 In multivariate analysis, baseline sVEGFR-3 and IL-8 remained independent predictors of OS in the sunitinib arm, while no independent predictors of outcome remained in the IFN-alpha arm. Sunitinib 98-107 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 24557443-5 2014 The average weight percentage of fluoride for all F-varnishes containing NaF ranged from 2.03 to 2.24% F, which is within 90% of the declared label concentration of 2.26% F. Analysis of the difluorosilane-containing product required an additional hydrolysis step. Fluorides 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 23787997-5 2014 MTX stimulated the production of CXCL8 by human cancer cells in vitro and that of Cxcl2 by murine tumors in vivo. Mitoxantrone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 23787997-6 2014 The knockdown of CXCL8/Cxcl2 receptors (CXCR1/Cxcr1 and Cxcr2) reduced MTX-induced CRT exposure in both human and murine cancer cells, as well as the capacity of the latter-on exposure to MTX-to elicit an anticancer immune response in vivo. Mitoxantrone 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 17-22 23787997-6 2014 The knockdown of CXCL8/Cxcl2 receptors (CXCR1/Cxcr1 and Cxcr2) reduced MTX-induced CRT exposure in both human and murine cancer cells, as well as the capacity of the latter-on exposure to MTX-to elicit an anticancer immune response in vivo. Mitoxantrone 188-191 C-X-C motif chemokine ligand 8 Homo sapiens 17-22 25382335-10 2014 The mRNA expressions of IL-1alpha, IL-6, IL-8, and TNF-a in different concentrations of SDBS at different time were comparable with that of controls. dodecylbenzenesulfonic acid 88-92 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 24877120-5 2014 SLURP-1 diminished the TLR9-dependent secretion of IL-8 by CCL-241, and IFN gamma-induced upregulation of ICAM-1 in both IEC types. Cefaclor 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 24877120-6 2014 rSLURP-2 inhibited IL-1 beta-induced secretion of IL-6 and TLR4- and TLR9-dependent induction of CXCL10 and IL-8, respectively, in CCL-241. Cefaclor 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 25059554-0 2014 Nicotine induces the production of IL-1beta and IL-8 via the alpha7 nAChR/NF-kappaB pathway in human periodontal ligament cells: an in vitro study. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 25059554-6 2014 RESULTS: Compared with the control group, nicotine could significantly induce production of IL-1beta and IL-8 in human PDL cells and cause the similar effects on the expression of the NF-kappaB p65 subunit and NF-kappaB activity. Nicotine 42-50 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 25059554-7 2014 CONCLUSION: This study demonstrates that nicotine could induce production of IL-1beta and IL-8 via the alpha7 nAChR/NF-kappaB pathway in human PDL cells, providing data for a better understanding of the relationships among smoking, nicotine, and periodontitis. Nicotine 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 25059554-7 2014 CONCLUSION: This study demonstrates that nicotine could induce production of IL-1beta and IL-8 via the alpha7 nAChR/NF-kappaB pathway in human PDL cells, providing data for a better understanding of the relationships among smoking, nicotine, and periodontitis. Nicotine 232-240 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 25430458-10 2014 According to the results found in human THP-1 cells, levels of NF-kappaB and IL-8 in LPS group were significantly increased compared with those of the control group (P < 0.05); when compared with those in LPS group, levels of NF-kappaB in LPS+HDX group further increased significantly (P < 0.05); however, the NF-kappaB levels of LPS+SO2 group decreased significantly (P < 0.05). Sulfur Dioxide 340-343 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 24096876-10 2014 mRNA and protein expression of TNF-alpha, IL-8, and IL-6 in cells treated with DCA alone were up-regulated, and intra-cellular ROS and p-NF-kappaB p65 protein levels were also increased. Deoxycholic Acid 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 23844733-5 2014 CXC chemokines (such as interleukin-8) are bound to glycosaminoglycans on the endothelial surface and activate captured neutrophils, inducing expression of integrins. Glycosaminoglycans 52-70 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 23959576-6 2014 Furthermore, interleukin 8, osteopontin, hepatocyte growth factor, and tissue inhibitors of metalloproteinases-1 in peripheral blood enable assessment of responsiveness to pazopanib treatment. pazopanib 172-181 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 24701591-3 2014 Arterial calcification has been also determined by CT, by (18)F-FDG PET and also in the last few years by (18)F-sodium fluoride (NaF) PET. Sodium Fluoride 112-127 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 24161763-7 2014 Exogenous IL-8 increased the SP fraction and expression of multidrug resistance-1, decreasing the drug sensitivity. sp 29-31 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 24488902-10 2014 Tiopronin can reduce the levels of ET, leptin, IL-6 and IL-8 for treatment of NAFLD. Tiopronin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 24309288-4 2014 Sodium iodate-mediated RPE cell death was associated with increased levels of reactive oxygen species (ROS) and IL-8. sodium iodate 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 24309288-5 2014 Resveratrol, a natural occurring polyphenol compound, was found to strongly protect RPE cells from sodium iodate with inhibition of production of ROS and IL-8. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 24309288-10 2014 Moreover, PPAR agonists reversed sodium iodate-induced production of IL-8. sodium iodate 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 24056816-5 2014 In vitro, busulfan elicits pro-inflammatory activation (increased NF-KappaB activity and interleukin-8 expression) in human hepatoma cells. Busulfan 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 24701591-5 2014 Fluorine-18-NaF uptake in the heart and aorta increased significantly with advancing age. Fluorine-18 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 24739825-7 2014 Furthermore, after pretreatment of Ec109 cells with the specific p38 MAPK inhibitor SB203580, Ec109 cells proliferation and IL-8 secretion were inhibited. SB 203580 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 24297055-9 2014 RESULTS: Muramyl dipeptide-induced increases in NOD2, interleukin-8, and CXCL3 expression were inversely associated with miRNA expression. Dipeptides 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 24126532-5 2014 We found that HbR induced interleukin-8 (IL-8) production in the human gingival epithelial cell line Ca9-22. Hydrobromic Acid 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 26-39 24126532-5 2014 We found that HbR induced interleukin-8 (IL-8) production in the human gingival epithelial cell line Ca9-22. Hydrobromic Acid 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 24126532-7 2014 Inhibitors of p38 MAPK (SB203580) and Erk1/2 (PD98059) blocked HbR-induced IL-8 production. SB 203580 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 24126532-7 2014 Inhibitors of p38 MAPK (SB203580) and Erk1/2 (PD98059) blocked HbR-induced IL-8 production. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 46-53 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 24126532-7 2014 Inhibitors of p38 MAPK (SB203580) and Erk1/2 (PD98059) blocked HbR-induced IL-8 production. Hydrobromic Acid 63-66 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 24126532-8 2014 Additionally, HbR stimulated the translocation of NF-kappaB-p65 to the nucleus, consistent with enhancement of IL-8 expression by activation of the NF-kappaB pathway. Hydrobromic Acid 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 24126532-9 2014 In addition, small interfering RNA (siRNA) targeting activating transcription factor 2 (ATF-2) or cyclic AMP-response element-binding protein (CREB) inhibited HbR-induced IL-8 production. Hydrobromic Acid 159-162 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 24297055-10 2014 Overexpression of miR-192, miR-495, miR-512, and miR-671 suppressed NOD2 expression, muramyl dipeptide-mediated NF-kappaB activation, and messenger RNA expressions of interleukin-8 and CXCL3 in HCT116 cells. Dipeptides 93-102 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 24346217-7 2014 ELISA confirmed the protective effect of insulin and SP600125 on Abeta-induced expression of interleukin (IL)-8 and Growth related oncogene-alpha (Gro-alpha). pyrazolanthrone 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 93-111 24126532-11 2014 Combined pretreatment with an inhibitor of NF-kappaB (BAY11-7082) and SB203580 was more efficient in inhibiting the ability of HbR to induce IL-8 production than pretreatment with either BAY11-7082 or SB203580 alone. 3-(4-methylphenylsulfonyl)-2-propenenitrile 54-64 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 24126532-11 2014 Combined pretreatment with an inhibitor of NF-kappaB (BAY11-7082) and SB203580 was more efficient in inhibiting the ability of HbR to induce IL-8 production than pretreatment with either BAY11-7082 or SB203580 alone. SB 203580 70-78 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 24126532-11 2014 Combined pretreatment with an inhibitor of NF-kappaB (BAY11-7082) and SB203580 was more efficient in inhibiting the ability of HbR to induce IL-8 production than pretreatment with either BAY11-7082 or SB203580 alone. Hydrobromic Acid 127-130 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 23826669-0 2014 Palmitate induces interleukin-8 expression in human aortic vascular smooth muscle cells via Toll-like receptor 4/nuclear factor-kappaB pathway (TLR4/NF-kappaB-8). Palmitates 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 24366255-7 2014 IL-8(r=0.35-0.47) and TNF (r=0.42-0.53) expression levels exhibited strong correlations with the leukotriene genes. Leukotrienes 97-108 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24366255-10 2014 CONCLUSIONS: Leukotrienes and inflammatory genes, in particular, LTA4H and IL-8, exhibit close association in subjects with cardiovascular disease. Leukotrienes 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 23826669-4 2014 The aim of this study was to investigate the regulation of IL-8 expression by free fatty acids and determine the underlying mechanisms in HVSMCs. Fatty Acids, Nonesterified 78-94 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 23826669-6 2014 RESULTS: Palmitate induced IL-8 mRNA expression and secretion in a dose-dependent manner. Palmitates 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 23826669-8 2014 Parthenolide pretreatment also abolished IL-8 mRNA and protein induction by palmitate. parthenolide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 23826669-8 2014 Parthenolide pretreatment also abolished IL-8 mRNA and protein induction by palmitate. Palmitates 76-85 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 23826669-10 2014 Inhibition of protein kinase C (PKC) activation with calphostin C and chelerythrine partially suppressed palmitate-stimulated IL-8 expression, but it had no effect on palmitate-induced NF-kappaB activation. calphostin C 53-65 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 23826669-10 2014 Inhibition of protein kinase C (PKC) activation with calphostin C and chelerythrine partially suppressed palmitate-stimulated IL-8 expression, but it had no effect on palmitate-induced NF-kappaB activation. chelerythrine 70-83 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 23826669-10 2014 Inhibition of protein kinase C (PKC) activation with calphostin C and chelerythrine partially suppressed palmitate-stimulated IL-8 expression, but it had no effect on palmitate-induced NF-kappaB activation. Palmitates 105-114 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 23826669-11 2014 Finally, knockdown of TLR4 markedly abolished palmitate-induced NF-kappaB activation and IL-8 expression. Palmitates 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 23826669-12 2014 CONCLUSIONS: Palmitate induces IL-8 gene expression in HVSMCs through the TLR4/NF-kappaB pathway. Palmitates 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 24555677-7 2014 Exposure of THP-1 cells to both sizes of ZnO stimulated and increased release of proinflammatory cytokines interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha, and IL-6, as well as chemokine IL-8, and upregulated the expression of monocyte chemoattractant protein-1 and cyclooxygenase-2 genes. Zinc Oxide 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 24277696-6 2014 The thrombin-induced increases in IL-8/CXCL8 release and IL-8/CXCL8-luciferase were also inhibited by MEKK1 siRNA, PD98059 (an MEK inhibitor), U0126 (an ERK inhibitor), and RSK1 siRNA. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 24277696-6 2014 The thrombin-induced increases in IL-8/CXCL8 release and IL-8/CXCL8-luciferase were also inhibited by MEKK1 siRNA, PD98059 (an MEK inhibitor), U0126 (an ERK inhibitor), and RSK1 siRNA. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 39-44 24277696-6 2014 The thrombin-induced increases in IL-8/CXCL8 release and IL-8/CXCL8-luciferase were also inhibited by MEKK1 siRNA, PD98059 (an MEK inhibitor), U0126 (an ERK inhibitor), and RSK1 siRNA. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 24277696-6 2014 The thrombin-induced increases in IL-8/CXCL8 release and IL-8/CXCL8-luciferase were also inhibited by MEKK1 siRNA, PD98059 (an MEK inhibitor), U0126 (an ERK inhibitor), and RSK1 siRNA. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 24277696-6 2014 The thrombin-induced increases in IL-8/CXCL8 release and IL-8/CXCL8-luciferase were also inhibited by MEKK1 siRNA, PD98059 (an MEK inhibitor), U0126 (an ERK inhibitor), and RSK1 siRNA. U 0126 143-148 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 24277696-6 2014 The thrombin-induced increases in IL-8/CXCL8 release and IL-8/CXCL8-luciferase were also inhibited by MEKK1 siRNA, PD98059 (an MEK inhibitor), U0126 (an ERK inhibitor), and RSK1 siRNA. U 0126 143-148 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 24277696-6 2014 The thrombin-induced increases in IL-8/CXCL8 release and IL-8/CXCL8-luciferase were also inhibited by MEKK1 siRNA, PD98059 (an MEK inhibitor), U0126 (an ERK inhibitor), and RSK1 siRNA. U 0126 143-148 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 24163441-8 2014 Although methacholine and U46619 induced interleukin-8 (IL-8) release and this was inhibited by RGS2 overexpression, the repression of U46619-induced IL-8 release by salmeterol plus dexamethasone was unaffected by RGS2 knockdown. Methacholine Chloride 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 41-54 24163441-8 2014 Although methacholine and U46619 induced interleukin-8 (IL-8) release and this was inhibited by RGS2 overexpression, the repression of U46619-induced IL-8 release by salmeterol plus dexamethasone was unaffected by RGS2 knockdown. Methacholine Chloride 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 24163441-8 2014 Although methacholine and U46619 induced interleukin-8 (IL-8) release and this was inhibited by RGS2 overexpression, the repression of U46619-induced IL-8 release by salmeterol plus dexamethasone was unaffected by RGS2 knockdown. 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 41-54 24163441-8 2014 Although methacholine and U46619 induced interleukin-8 (IL-8) release and this was inhibited by RGS2 overexpression, the repression of U46619-induced IL-8 release by salmeterol plus dexamethasone was unaffected by RGS2 knockdown. 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 24163441-8 2014 Although methacholine and U46619 induced interleukin-8 (IL-8) release and this was inhibited by RGS2 overexpression, the repression of U46619-induced IL-8 release by salmeterol plus dexamethasone was unaffected by RGS2 knockdown. Salmeterol Xinafoate 166-176 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 24163441-8 2014 Although methacholine and U46619 induced interleukin-8 (IL-8) release and this was inhibited by RGS2 overexpression, the repression of U46619-induced IL-8 release by salmeterol plus dexamethasone was unaffected by RGS2 knockdown. Dexamethasone 182-195 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 25119735-0 2014 Regulation of IL-8 promoter activity by verrucarin A in human monocytic THP-1 cells. muconomycin A 40-52 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 25119735-8 2014 Mutation of the CCAAT/enhancer-binding protein (CEBP) beta binding site of the IL-8 promoter affected only DON-, but not VA- and TNFalpha-induced luciferase expression. deoxynivalenol 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 25268553-3 2014 This study focused on examining the adverse effects of inorganic fluoride (NaF) on human lymphocyte cells in vitro. inorganic fluoride 55-73 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 26054180-13 2014 CONCLUSION: The Enamelon products (970 ppm and 1150 ppm F- ion, SnF2 OTC dentifrices) delivering ACP were statistically significantly more effective in reducing enamel solubility than two Rx strength 5000 ppm F- ion NaF toothpastes containing TCP and the Rx 900 ppm F- ion NaF paste containing CPP-ACP. amorphous calcium phosphate 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 216-219 26054180-13 2014 CONCLUSION: The Enamelon products (970 ppm and 1150 ppm F- ion, SnF2 OTC dentifrices) delivering ACP were statistically significantly more effective in reducing enamel solubility than two Rx strength 5000 ppm F- ion NaF toothpastes containing TCP and the Rx 900 ppm F- ion NaF paste containing CPP-ACP. amorphous calcium phosphate 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 273-276 24336915-0 2014 Reduction of interleukin 8 and platelet-derived growth factor levels by topical ketorolac, 0.45%, in patients with diabetic retinopathy. Ketorolac 80-89 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 24336915-8 2014 Levels of IL-8 (41% reduction; P = .002) and PDGF-AA (21% reduction; P = .009) were significantly lower in the vitreous of patients treated with ketorolac. Ketorolac 145-154 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 24336915-9 2014 CONCLUSIONS AND RELEVANCE: Topical ketorolac tromethamine, 0.45%, significantly lowered aqueous IL-8 levels and vitreous IL-8 and PDGF-AA levels in this series of eyes, suggesting that it may cause meaningful inhibition of inflammatory cytokines implicated in the pathogenesis of DR. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01609881. Ketorolac Tromethamine 35-57 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 24336915-9 2014 CONCLUSIONS AND RELEVANCE: Topical ketorolac tromethamine, 0.45%, significantly lowered aqueous IL-8 levels and vitreous IL-8 and PDGF-AA levels in this series of eyes, suggesting that it may cause meaningful inhibition of inflammatory cytokines implicated in the pathogenesis of DR. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01609881. Ketorolac Tromethamine 35-57 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 25165413-7 2014 Our findings suggest a novel role for paeonol in alleviating the oxidative stress and lung inflammation induced by chronic CS exposure in vivo and in suppressing CSE-induced IL-8 in vitro via its antioxidant function and an inhibition of the MAPKs/NF-kappaB signaling. paeonol 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 24864134-4 2014 Furthermore, 2-Cl-IB-MECA significantly decreased TNF-alpha-stimulated IL-8 and IL-1beta mRNA expression and secretion, compared to the TNF-alpha-only treated group. 2-chloro-N(6)-(3-iodobenzyl)adenosine-5'-N-methyluronamide 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 25484047-9 2014 The IL-8 binding site of CXCR2 was identified by screening peptide libraries with the IL-8 ligand, and then reconstructed as soluble synthetic peptides. Peptides 143-151 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 25484064-4 2014 The hybridoma-derived antibody fully inhibited IL-8 and Gro-alpha responses in calcium flux and beta-arrestin recruitment assays. Calcium 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 24908306-4 2014 Binding of the IL-8 ligand to the CXCR2 receptor results in an intracellular signaling pathway mediated by GTP binding proteins coupled to the receptor itself. Guanosine Triphosphate 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 25530684-5 2014 EXPERIMENTAL APPROACH: Time course and dose-dependent release of interleukin- (IL-) 6 and IL-8 from A549 were measured after pretreatment of A549 with EtP (2.5-10 mM), sodium pyruvate (NaP, 10 mM), or EtOH (85-170 mM), and subsequent lipopolysaccharide or IL-1beta stimulation. ethyl pyruvate 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 25530684-7 2014 KEY RESULTS: Treating A549 with EtOH or EtP reduced substantially the cytokine-induced release of IL-8 and IL-6. Ethanol 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 25530684-7 2014 KEY RESULTS: Treating A549 with EtOH or EtP reduced substantially the cytokine-induced release of IL-8 and IL-6. ethyl pyruvate 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 25580060-8 2014 IL-8, NE, MMP-9, HA, and type IV collagen in sputum were also decreased in roxithromycin group compared with the control group (all P < 0.01). Roxithromycin 75-88 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24326457-3 2014 With tunable nanoscopic sizes, negligible cytotoxicity and remarkable degradability, they are able to encapsulate doxorubicin (Dox) with inner cavities and bind interleukin-8 (IL-8) small interfering RNA (siRNA) with cationic shells. Doxorubicin 114-125 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 24326457-3 2014 With tunable nanoscopic sizes, negligible cytotoxicity and remarkable degradability, they are able to encapsulate doxorubicin (Dox) with inner cavities and bind interleukin-8 (IL-8) small interfering RNA (siRNA) with cationic shells. Doxorubicin 114-125 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 24326457-3 2014 With tunable nanoscopic sizes, negligible cytotoxicity and remarkable degradability, they are able to encapsulate doxorubicin (Dox) with inner cavities and bind interleukin-8 (IL-8) small interfering RNA (siRNA) with cationic shells. Doxorubicin 127-130 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 24326457-3 2014 With tunable nanoscopic sizes, negligible cytotoxicity and remarkable degradability, they are able to encapsulate doxorubicin (Dox) with inner cavities and bind interleukin-8 (IL-8) small interfering RNA (siRNA) with cationic shells. Doxorubicin 127-130 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 24326457-5 2014 In vitro studies also showed that the NCs loaded with Dox, IL-8 siRNA and both agents can be readily taken up by PC3 prostate cancer cells, resulting in a significant chemotherapeutic effect and/or IL-8 gene silencing. Doxorubicin 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 24697659-4 2014 Among the isolates, three pentacyclic triterpenoids, ursolic acid (1), asiatic acid (3) and terminolic acid (6), together with one tannin casuarinin (17), were found to significantly decrease interleukin-8 (IL-8) production in human colon cancer cells. pentacyclic 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 192-205 24697659-4 2014 Among the isolates, three pentacyclic triterpenoids, ursolic acid (1), asiatic acid (3) and terminolic acid (6), together with one tannin casuarinin (17), were found to significantly decrease interleukin-8 (IL-8) production in human colon cancer cells. pentacyclic 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 24697659-4 2014 Among the isolates, three pentacyclic triterpenoids, ursolic acid (1), asiatic acid (3) and terminolic acid (6), together with one tannin casuarinin (17), were found to significantly decrease interleukin-8 (IL-8) production in human colon cancer cells. triterpenoids 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 192-205 24697659-4 2014 Among the isolates, three pentacyclic triterpenoids, ursolic acid (1), asiatic acid (3) and terminolic acid (6), together with one tannin casuarinin (17), were found to significantly decrease interleukin-8 (IL-8) production in human colon cancer cells. triterpenoids 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 24697659-4 2014 Among the isolates, three pentacyclic triterpenoids, ursolic acid (1), asiatic acid (3) and terminolic acid (6), together with one tannin casuarinin (17), were found to significantly decrease interleukin-8 (IL-8) production in human colon cancer cells. terminolic acid 92-107 C-X-C motif chemokine ligand 8 Homo sapiens 192-205 24697659-4 2014 Among the isolates, three pentacyclic triterpenoids, ursolic acid (1), asiatic acid (3) and terminolic acid (6), together with one tannin casuarinin (17), were found to significantly decrease interleukin-8 (IL-8) production in human colon cancer cells. terminolic acid 92-107 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 25242873-0 2014 Purine-metabolizing ectoenzymes control IL-8 production in human colon HT-29 cells. purine 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 25242873-6 2014 In response to poly (I:C), with or without ATP and/or ADP, HT-29 cells released IL-8 and this secretion was modulated by the presence of NTPDase2 and adenylate kinase. poly 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 25242873-6 2014 In response to poly (I:C), with or without ATP and/or ADP, HT-29 cells released IL-8 and this secretion was modulated by the presence of NTPDase2 and adenylate kinase. Adenosine Triphosphate 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 25242873-6 2014 In response to poly (I:C), with or without ATP and/or ADP, HT-29 cells released IL-8 and this secretion was modulated by the presence of NTPDase2 and adenylate kinase. Adenosine Diphosphate 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 24908314-3 2014 We have recently shown that proteasome inhibition by bortezomib (BZ) specifically increases IL-8 release from metastatic prostate and ovarian cancer cells. Bortezomib 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 24908314-3 2014 We have recently shown that proteasome inhibition by bortezomib (BZ) specifically increases IL-8 release from metastatic prostate and ovarian cancer cells. Bortezomib 65-67 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 24908314-5 2014 IL-8 is localized in the cytoplasm in both cell types, and its protein levels are significantly increased by BZ. Bortezomib 109-111 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24908316-0 2014 Quantitative analysis of bortezomib-induced IL-8 gene expression in ovarian cancer cells. Bortezomib 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 24908316-5 2014 We have recently shown that in ovarian cancer cells, BZ greatly increases IL-8 expression, while expression of other NFkappaB-regulated cytokines, IL-6 and TNF, is unchanged. Bortezomib 53-55 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24908316-6 2014 In this chapter, we describe a protocol that uses real-time qRT-PCR to quantitatively analyze mRNA levels of IL-8 and IL-6 in BZ-treated ovarian cancer cells. Bortezomib 126-128 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 24201777-8 2014 This effect was related to inhibition of gemcitabine-induced NF-kappaB activation by gabexate mesilate, which prevented RelA/p65 nuclear translocation and resulted in metalloproteinase 2, metalloproteinase 9, vascular endothelial growth factor, and interleukin 8 down-regulation. gemcitabine 41-52 C-X-C motif chemokine ligand 8 Homo sapiens 249-262 24201777-8 2014 This effect was related to inhibition of gemcitabine-induced NF-kappaB activation by gabexate mesilate, which prevented RelA/p65 nuclear translocation and resulted in metalloproteinase 2, metalloproteinase 9, vascular endothelial growth factor, and interleukin 8 down-regulation. Gabexate 85-102 C-X-C motif chemokine ligand 8 Homo sapiens 249-262 24988605-8 2014 Inhibitors of CXCL8 (such as N-acetyl-L-cysteine) cause a decrease of exacerbation frequency and clinical symptoms. Acetylcysteine 29-48 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 25026798-8 2014 Quantitative analysis of urinary IL-6, IL-8, and VEGF levels in patients with SDS may be used to evaluate tubulointerstitial inflammation and to predict the development of interstitial fibrosis. sds 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 25254233-3 2014 Wet sieving aggregate analysis showed significantly better fragmentation in the NaF, Na-hexa-metaphosphate, and ryegrass root solutions with a mean weight diameter range of 15.5-18.8 mm compared to the 44.2-47.9 mm of the poultry manure, ADB, and FBC treatments. adb 238-241 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 25254233-3 2014 Wet sieving aggregate analysis showed significantly better fragmentation in the NaF, Na-hexa-metaphosphate, and ryegrass root solutions with a mean weight diameter range of 15.5-18.8 mm compared to the 44.2-47.9 mm of the poultry manure, ADB, and FBC treatments. 4-(3,5-difluorophenyl)benzoic acid 247-250 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 24134915-2 2013 Flavone effects were assessed on soluble pro-inflammatory mediator (IL-8, IL-6, macrophage chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2)-derived PGE2) production and on nuclear factor (NF)-kappaB activation in 3d-confluent and 21d-differentiated Caco-2 cells stimulated with interleukin (IL)-1beta. flavone 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 25509145-4 2014 Comprehensive assessment of the results after has shown that 3-day HUVEC cultivating in the presence of 1% O2 led to pathological activation of endotheliocytes: increased NO synthesis combined with the marked secretion of endothelin-1, IL-6, IL-8 and TNF-alpha, sVCAM-1, sE-cadherin and of sE-selectin, VEGF-A and bFGF, and slow proliferation. Oxygen 107-109 C-X-C motif chemokine ligand 8 Homo sapiens 242-246 24502918-4 2014 In this study, when human mast cells (HMC-1 cells) were stimulated with SPs collected from pathogenic wild-type amoebae, interleukin IL-8 mRNA expression and production were significantly increased compared with cells incubated with medium alone. Sodium phenolsulfonate 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 24502918-5 2014 Inhibition of CP activity in the SPs with heat or the CP inhibitor E64 resulted in significant reduction of IL-8 production. Sodium phenolsulfonate 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 24502918-5 2014 Inhibition of CP activity in the SPs with heat or the CP inhibitor E64 resulted in significant reduction of IL-8 production. E 64 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 24502918-6 2014 Moreover, SPs obtained from inhibitors of cysteine protease (ICP)-overexpressing amoebae with low CP activity showed weaker stimulatory effects on IL-8 production than the wild-type control. Sodium phenolsulfonate 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 24101016-9 2014 CONCLUSION: In this substudy of a randomized trial comparing minimally invasive and conventional open esophagectomies for cancer, significantly better preserved leukocyte counts and IL-8 levels were observed in the MIE group compared to the open group. mie 215-218 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 24340081-11 2013 Stimulation of human bronchial cells by AFL led to IL-8 production in a dose-dependent manner. aflatoxicol 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 24080332-3 2013 Following screening of fifteen metals, zinc and nickel were identified with a marked proinflammatory effect, as determined by ICAM-1 and IL-8 induction, on human umbilical vein endothelial cells (HUVECs). Nickel 48-54 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 24080332-5 2013 Blockage of TLR-4 signaling by CLI-095, a TLR-4 inhibitor, completely inhibited the nickel-induced ICAM-1 and IL-8 expression and NFkappaB activation. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 24080332-5 2013 Blockage of TLR-4 signaling by CLI-095, a TLR-4 inhibitor, completely inhibited the nickel-induced ICAM-1 and IL-8 expression and NFkappaB activation. Nickel 84-90 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 24080332-6 2013 The same CLI-095 treatment significantly blocked the zinc-induced IL-8 expression, however with no significant effect on the ICAM-1 expression and a minor inhibitory effect on the NFkappaB activation. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 24080355-4 2013 Moreover, BbV was able to stimulate neutrophil release of proinflammatory mediators such as IL-8 and IL-6 as well as PGE2 and NETs liberation. BENZYL 2-ACETAMIDO-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 23994500-11 2013 The organophosphourus compounds affected the release of inflammatory cytokines, such as IL-1ss and IL-8. organophosphourus 4-21 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 24075485-9 2013 The sivelestat group also showed significantly lower plasma levels of interleukin-8 immediately after bypass (p = 0.041) and interleukin-10 at 15 minutes after removal of the aortic cross-clamp (p = 0.048), and immediately after bypass (p = 0.037). sivelestat 4-14 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 24060240-8 2013 IL-8 production stimulated with LPS was diminished by vitamin D3 derivatives. Cholecalciferol 54-64 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24060240-10 2013 The anti-inflammatory effect of vitamin D3 derivatives was thus associated with diminution of IL-8 production due to increased release of sCD14. Cholecalciferol 32-42 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 24339939-12 2013 This effect is mediated through the CXCR2 ligands (ENA78, GRO-alpha and IL-8) produced by BSMC. bsmc 90-94 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 24060240-0 2013 Vitamin D3 derivatives increase soluble CD14 release through ERK1/2 activation and decrease IL-8 production in intestinal epithelial cells. Cholecalciferol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 24071475-1 2013 Recognition of the harmful effects of sodium fluoride (NaF) on human reproduction is increasing, especially as it relates to female reproduction. Sodium Fluoride 38-53 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 24298938-4 2013 We found that andrographolide pretreatment significantly restored the glutathione level in CSE-exposed A549 cells, coupled with reduced inhibitor kappaB (IkappaB)-alpha phosphorylation and p65 nuclear translocation and interleukin (IL)-8 and IL-6 secretion. andrographolide 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 219-237 24298938-8 2013 In contrast, miR-218 silencing enhanced IkappaB-alpha phosphorylation and p65 nuclear accumulation in cells with andrographolide pretreatment and reversed andrographolide-mediated reduction of IL-6 and IL-8 production. andrographolide 113-128 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 24298938-8 2013 In contrast, miR-218 silencing enhanced IkappaB-alpha phosphorylation and p65 nuclear accumulation in cells with andrographolide pretreatment and reversed andrographolide-mediated reduction of IL-6 and IL-8 production. andrographolide 155-170 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 23670201-11 2013 Regarding the mechanism of PM2.5 uptake, in both THP-1 and A549 cells, cytochalasin D prevented PM2.5-induced IL-8 mRNA expression and cytokine release, indicating a key role for actin polymerization in particles uptake and that the production of IL-8 correlated with particle phagocytosis. Cytochalasin D 71-85 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 23670201-11 2013 Regarding the mechanism of PM2.5 uptake, in both THP-1 and A549 cells, cytochalasin D prevented PM2.5-induced IL-8 mRNA expression and cytokine release, indicating a key role for actin polymerization in particles uptake and that the production of IL-8 correlated with particle phagocytosis. Cytochalasin D 71-85 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 23670201-12 2013 As signal transduction pathway involvement, in both THP-1 and A549 cells, PM2.5-induced IL-8 release could be completely blocked by the selective inhibitor SB203580, indicating a role of p38 MAPK activation. SB 203580 156-164 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 24032673-3 2013 In the present study, we show in neutrophil-activating chemokine CXCL8 that the highly conserved GP (glycine-proline) motif located distal to both N-terminal and N-loop residues couples Site-I and Site-II interactions. Glycine 101-108 C-X-C motif chemokine ligand 8 Homo sapiens 65-70 24032673-3 2013 In the present study, we show in neutrophil-activating chemokine CXCL8 that the highly conserved GP (glycine-proline) motif located distal to both N-terminal and N-loop residues couples Site-I and Site-II interactions. Proline 109-116 C-X-C motif chemokine ligand 8 Homo sapiens 65-70 23933845-3 2013 The aim of this study was to explore the effects of PT and the peptidomimetic natural products, Dhurrin and Prunasin, on the expression of the IL-6, IL-8, IL-23, HSP70 and ICAM-1 on IFN-gamma and TNF-alpha-NHEK activated cells. Peptide T 52-54 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 24385947-6 2013 BIRB 796 reduced LPS-mediated IL-8 production in THP-1 cells but not in Raw 264.7 cells. birb 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 24465106-7 2013 At day 4, IL-8 mean values increased for both IVFO and control groups. ivfo 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 23820266-0 2013 gamma-Glutamyltransferase catabolism of S-nitrosoglutathione modulates IL-8 expression in cystic fibrosis bronchial epithelial cells. S-Nitrosoglutathione 40-60 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 23820266-2 2013 A role for GSNO has been envisaged in the expression of inflammatory cytokines such as IL-8; however, conflicting results have been reported. S-Nitrosoglutathione 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 23820266-5 2013 This study was aimed at evaluating the effect of GSNO catabolism mediated by GGT on production of IL-8 in CF transmembrane regulation protein-mutated IB3-1 bronchial cells. S-Nitrosoglutathione 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 23820266-6 2013 The rapid, GGT-catalyzed catabolism of GSNO caused a decrease in both basal and lipopolysaccharide-stimulated IL-8 production in IB3-1 cells, by modulating both NF-kappaB and ERK1/2 pathways, along with a decrease in cell proliferation. S-Nitrosoglutathione 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 23820266-7 2013 In contrast, a slow decomposition of GSNO produced a significant increase in both cell proliferation and expression of IL-8, the latter possibly through p38-mediated stabilization of IL-8 mRNA. S-Nitrosoglutathione 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 23820266-7 2013 In contrast, a slow decomposition of GSNO produced a significant increase in both cell proliferation and expression of IL-8, the latter possibly through p38-mediated stabilization of IL-8 mRNA. S-Nitrosoglutathione 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 23820266-8 2013 Our data suggest that the differential GSNO catabolism mediated by GGT enzyme activity can downregulate the production of IL-8 in CF cells. S-Nitrosoglutathione 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 23775574-8 2013 And also immune reaction was less in patients exposed to desflurane anesthesia when compared to propofol anesthesia as indicated by lower plasma concentrations of IL-8 and IL-6. Desflurane 57-67 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 23775574-8 2013 And also immune reaction was less in patients exposed to desflurane anesthesia when compared to propofol anesthesia as indicated by lower plasma concentrations of IL-8 and IL-6. Propofol 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 24157330-6 2013 Using an antibody array approach, curcumin was found to inhibit LPS-induced cytokine production, including MIP-1alpha, MIP-1beta, IL-6, IL-8 (CXCL-8) and GRO-alpha. Curcumin 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 23933845-3 2013 The aim of this study was to explore the effects of PT and the peptidomimetic natural products, Dhurrin and Prunasin, on the expression of the IL-6, IL-8, IL-23, HSP70 and ICAM-1 on IFN-gamma and TNF-alpha-NHEK activated cells. dhurrin 96-103 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 24157330-6 2013 Using an antibody array approach, curcumin was found to inhibit LPS-induced cytokine production, including MIP-1alpha, MIP-1beta, IL-6, IL-8 (CXCL-8) and GRO-alpha. Curcumin 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 142-148 24157330-7 2013 The inhibitory effect of curcumin on IL-8 production was confirmed by ELISA. Curcumin 25-33 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 23933845-3 2013 The aim of this study was to explore the effects of PT and the peptidomimetic natural products, Dhurrin and Prunasin, on the expression of the IL-6, IL-8, IL-23, HSP70 and ICAM-1 on IFN-gamma and TNF-alpha-NHEK activated cells. prunasin 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 23078188-6 2013 However, only ZnO NPs increased ROS and induced IL-8 release both after 6 and 24 h. Experimental data indicate a main role of chemical composition and solubility in ZnO NPs toxicity. Zinc Oxide 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 24431789-1 2013 The objective of this study was to evaluate the effect of the addition of stannous fluoride (SnF2) and sodium fluoride (NaF) to luting cements on the retention of provisional crowns. Sodium Fluoride 103-118 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 24011765-8 2013 In children with C difficile infection, fecal CXCL-5 and IL-8 messenger RNA abundances at diagnosis correlated with persistent diarrhea after 5 days of C difficile infection therapy and with treatment with vancomycin. Vancomycin 206-216 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 24231103-6 2013 Intake of CLA-enriched butter increased the serum levels of anti-inflammatory IL-10 but reduced transcription factor NFkappaB in blood and serum levels of TNFalpha, IL-2, IL-8 and inactive metalloproteinase-9. Linoleic Acids, Conjugated 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 24145706-4 2013 Notably, the levels of interleukin (IL)-1beta, IL-8 and monocyte chemotactic protein-1 (MCP-1) in the ELF were significantly increased following the operations which involved the inhalation of sevoflurane and nitrous oxide, although the levels of these molecules were not significantly changed by the inhalation of sevoflurane and air. Sevoflurane 193-204 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 24145706-6 2013 These observations suggest that the combination of sevoflurane and nitrous oxide induces an inflammatory response (increased production of IL-1beta, IL-8 and MCP-1) and suppresses the anti-inflammatory response (reduced production of IL-12p70) in the local milieu of the airway. Sevoflurane 51-62 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 24080250-9 2013 Montelukast significantly suppressed the release of IL-8 (p = 0.016), IL-6 (p = 0.006), RANTES (p = 0.002) and IFN-gamma (p = 0.046), in a dose dependent manner in unstimulated cultures but not in those stimulated with IL-1/TNF. montelukast 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 24145706-6 2013 These observations suggest that the combination of sevoflurane and nitrous oxide induces an inflammatory response (increased production of IL-1beta, IL-8 and MCP-1) and suppresses the anti-inflammatory response (reduced production of IL-12p70) in the local milieu of the airway. Nitrous Oxide 67-80 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 23742950-7 2013 In human lung fibroblasts inhibition of COX with diclofenac was associated with increased release of IL-8 and IP-10. Diclofenac 49-59 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 24041966-7 2013 Moreover, PAC were highly resistant to complement-mediated lysis and primarily responded to human complement by releasing IL-6 and IL-8. pac 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 24080250-10 2013 Withdrawal of Montelukast treatment, was associated with increased IL-8 and RANTES secretion in unstimulated nasal AEC cultured from subjects with asthma and allergic rhinitis but not with asthma alone. montelukast 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 24080250-11 2013 CONCLUSIONS: Montelukast treatment for asthma symptoms reversibly suppresses nasal AEC release of pro-inflammatory mediators (i.e. IL-8 and RANTES) but only in those cells cultured from subjects with concomitant allergic rhinitis. montelukast 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 24285369-4 2013 Purified PMNs from diabetic patients who had been treated with glibenclamide (an ATP-sensitive potassium channel blocker for anti-diabetes therapy), showed reduction of interleukin (IL)-1beta and IL-8 secretion when exposed to B. pseudomallei. Glyburide 63-76 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 23933549-4 2013 Large equilibrium charge and small dynamic contributions are also characteristic of stretching vibrations in the ionic diatomic molecules, NaF, NaCl, LiF and LiCl. Lithium Chloride 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 24076166-10 2013 Carbocysteine in CSE stimulated bronchial epithelial cells, reduced: (1) TLR4, LPS binding and p21; (2) IL-8 mRNA and IL-8 release due to IL-1 stimulation; (3) neutrophil chemotactic migration. Carbocysteine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 24076166-10 2013 Carbocysteine in CSE stimulated bronchial epithelial cells, reduced: (1) TLR4, LPS binding and p21; (2) IL-8 mRNA and IL-8 release due to IL-1 stimulation; (3) neutrophil chemotactic migration. Carbocysteine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 23997175-8 2013 Silica exposure activated MAP kinases (ERK and p38) and altered the expression of transcription factors (nF-kappaB and NF-E2-related factor 2), proinflammatory cytokines (interleukin-8 and -6), and apoptotic proteins. Silicon Dioxide 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 171-191 24278446-4 2013 TcdA and TcdB alter cytoskeletal signaling and trigger the release of CXCL8/IL-8, a potent neutrophil chemoattractant, from intestinal epithelial cells; however, little is known about the surface receptor(s) that mediate these events. tcda 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 70-75 24278446-4 2013 TcdA and TcdB alter cytoskeletal signaling and trigger the release of CXCL8/IL-8, a potent neutrophil chemoattractant, from intestinal epithelial cells; however, little is known about the surface receptor(s) that mediate these events. tcda 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 24278446-4 2013 TcdA and TcdB alter cytoskeletal signaling and trigger the release of CXCL8/IL-8, a potent neutrophil chemoattractant, from intestinal epithelial cells; however, little is known about the surface receptor(s) that mediate these events. trimethylaminocarboxyldihydroboran 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 70-75 24278446-4 2013 TcdA and TcdB alter cytoskeletal signaling and trigger the release of CXCL8/IL-8, a potent neutrophil chemoattractant, from intestinal epithelial cells; however, little is known about the surface receptor(s) that mediate these events. trimethylaminocarboxyldihydroboran 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 24278446-5 2013 In the current study, we sought to assess whether toxin-induced CXCL8/IL-8 release and barrier dysfunction are driven by the activation of the P2Y6 receptor following the release of UDP, a danger signal, from intoxicated Caco-2 cells. Uridine Diphosphate 182-185 C-X-C motif chemokine ligand 8 Homo sapiens 64-69 24278446-7 2013 Toxin-induced CXCL8/IL-8 production and release were attenuated in the presence of a selective P2Y6 inhibitor (MRS2578). N,N''-1,4-butanediylbis(N'-(3-isothiocyanatophenyl))thiourea 111-118 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 24278446-7 2013 Toxin-induced CXCL8/IL-8 production and release were attenuated in the presence of a selective P2Y6 inhibitor (MRS2578). N,N''-1,4-butanediylbis(N'-(3-isothiocyanatophenyl))thiourea 111-118 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 24278446-11 2013 Taken together these data outline a novel role for the P2Y6 receptor in the induction of CXCL8/IL-8 production and barrier dysfunction in response to C. difficile toxin exposure and may provide a new therapeutic target for the treatment of CDI. 1,1'-Carbonyldiimidazole 240-243 C-X-C motif chemokine ligand 8 Homo sapiens 89-94 24063987-13 2013 Evodiamine provoked IL-8 secretion via ERK1/2, SAPK/JNK, JAK2 and AP-1 pathways which could be counteracted by berberine. evodiamine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 24063987-13 2013 Evodiamine provoked IL-8 secretion via ERK1/2, SAPK/JNK, JAK2 and AP-1 pathways which could be counteracted by berberine. Berberine 111-120 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 24063987-14 2013 SIGNIFICANCE: Although showing anti-proliferative and anti-migratory activities in AGS cells, evodiamine displayed a potential tendency to promote metastasis of gastric cancer cells by increasing IL-8 secretion and adhesion molecules. evodiamine 94-104 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 24063987-0 2013 Berberine counteracts enhanced IL-8 expression of AGS cells induced by evodiamine. Berberine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 24063987-0 2013 Berberine counteracts enhanced IL-8 expression of AGS cells induced by evodiamine. evodiamine 71-81 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 24063987-1 2013 AIMS: Although showing an anti-tumor activity, evodiamine also up-regulated IL-8 production of human gastric cancer AGS cells. evodiamine 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 24063987-10 2013 IL-8 expression and the adhesive ability of AGS cells to HUVECs were significantly increased by evodiamine, but were inhibited after being co-treated with berberine in AGS cells. evodiamine 96-106 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24063987-10 2013 IL-8 expression and the adhesive ability of AGS cells to HUVECs were significantly increased by evodiamine, but were inhibited after being co-treated with berberine in AGS cells. Berberine 155-164 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24063987-11 2013 As IL-8 was neutralized, increased adhesion of AGS cells to HUVECs induced by evodiamine was abolished. evodiamine 78-88 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 24237854-7 2013 RESULTS: We found that in ASMCs the TLR3 agonist poly I:C induced IL-8 release was reduced while induced IL-6 release by the TLR7/8 agonist imiquimod was further increased by the presence of piclamilast. asmcs 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 24436991-5 2013 Isonahocol E(3) significantly inhibited ET-1-induced cell proliferation, as well as inflammatory mediators, such as interleukin-6 (IL-6) and interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha), and pro-angiogenic factors including metalloproteinases in immortalized human keratinocytes. isonahocol E(3) 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 141-154 24436991-5 2013 Isonahocol E(3) significantly inhibited ET-1-induced cell proliferation, as well as inflammatory mediators, such as interleukin-6 (IL-6) and interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha), and pro-angiogenic factors including metalloproteinases in immortalized human keratinocytes. isonahocol E(3) 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 24237854-7 2013 RESULTS: We found that in ASMCs the TLR3 agonist poly I:C induced IL-8 release was reduced while induced IL-6 release by the TLR7/8 agonist imiquimod was further increased by the presence of piclamilast. Poly I 49-55 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 24062309-6 2013 Antioxidants and low oxygen tension prevented SA IL-1alpha expression and restricted expression of SASP components IL-6 and IL-8. Oxygen 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 23877510-2 2013 Recently, a 64-year-old man with biopsy-proven lung cancer underwent an (18)F-NaF PET/CT bone scan due to a shortage of (99m)Tc. Technetium 125-127 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 24085292-4 2013 However, we found that long-term incubation with PIs (PS-341 or MG132) increased NF-kappaB-regulated gene expression such as COX-2, cIAP2, XIAP, and IL-8 in a dose- and time-dependent manner, which was mediated by phosphorylation of IkappaBalpha and its subsequent degradation via the alternative route, lysosome. Bortezomib 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 24085292-4 2013 However, we found that long-term incubation with PIs (PS-341 or MG132) increased NF-kappaB-regulated gene expression such as COX-2, cIAP2, XIAP, and IL-8 in a dose- and time-dependent manner, which was mediated by phosphorylation of IkappaBalpha and its subsequent degradation via the alternative route, lysosome. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 24085292-8 2013 Pretreatment with IKKbeta specific inhibitor, SC-514, partially suppressed IkappaBalpha degradation and IL-8 production by PIs. SC 514 46-52 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. Fluorine 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. Fluorine 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 219-222 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. Fluorine 136-144 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. Fluorine 136-144 C-X-C motif chemokine ligand 8 Homo sapiens 219-222 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. Borohydrides 157-169 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. Borohydrides 157-169 C-X-C motif chemokine ligand 8 Homo sapiens 219-222 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. boron trifluoride 227-230 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. closo-boranes 261-274 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 24071912-3 2013 After further heating, the fluorine substituted compound becomes X-ray amorphous and decomposes to NaF at ~310 C. This work shows that fluorine-substituted borohydrides tend to decompose to more stable compounds, e.g. NaF and BF3 or amorphous products such as closo-boranes, e.g. Na2B12H12. na2b12h12 281-290 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 24071912-6 2013 The reversible hydrogen storage capacity tends to decrease possibly due to the formation of NaF and Na2B12H12. Hydrogen 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 24071912-7 2013 On the other hand, the additive sodium fluoride appears to facilitate hydrogen uptake, prevent foaming, phase segregation and loss of material from the sample container for samples of NaBH4-NaF. Sodium Fluoride 32-47 C-X-C motif chemokine ligand 8 Homo sapiens 190-193 24179688-0 2013 Effect of cholesterol depletion on interleukin-8 production in human respiratory epithelial cells. Cholesterol 10-21 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 24179688-6 2013 Mitogen-activated protein kinase (MAPK) inhibitors were used to determine the upstream signaling pathway for IL-8 production in cholesterol-depleted cells. Cholesterol 128-139 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 24179688-8 2013 IL-8 production was increased in cholesterol-depleted A 549 cells and restored by cholesterol repletion. Cholesterol 33-44 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24179688-8 2013 IL-8 production was increased in cholesterol-depleted A 549 cells and restored by cholesterol repletion. Cholesterol 82-93 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24179688-9 2013 IL-8 production was decreased by pretreatment with the extracellular signal-regulated kinase (ERK) inhibitor U0126 but not with JNK inhibitor II or the p38 MAPK inhibitor SB202190. U 0126 109-114 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 24358628-13 2013 Lipoxin A4 inhibited tumor necrosis factor alpha-induced interleukin 8 release from airway epithelial cells via its receptor FPRL-1. lipoxin A4 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 23933110-0 2013 Luteolin 8-C-beta-fucopyranoside inhibits invasion and suppresses TPA-induced MMP-9 and IL-8 via ERK/AP-1 and ERK/NF-kappaB signaling in MCF-7 breast cancer cells. Tetradecanoylphorbol Acetate 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 23933110-3 2013 We investigated whether LU8C-FP would inhibit MMP-9 activation and IL-8 expression in 12-O-tetradecanoylphorbol-13-acetate (TPA)-treated MCF-7 breast cancer cells. lu8c-fp 24-31 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 23933110-3 2013 We investigated whether LU8C-FP would inhibit MMP-9 activation and IL-8 expression in 12-O-tetradecanoylphorbol-13-acetate (TPA)-treated MCF-7 breast cancer cells. Tetradecanoylphorbol Acetate 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 23933110-4 2013 LU8C-FP suppressed TPA-induced MMP-9 and IL-8 secretion and mRNA expression via inhibition of the MAPK signaling pathway and down-regulation of nuclear AP-1 and NF-kappaB. lu8c-fp 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 23933110-4 2013 LU8C-FP suppressed TPA-induced MMP-9 and IL-8 secretion and mRNA expression via inhibition of the MAPK signaling pathway and down-regulation of nuclear AP-1 and NF-kappaB. Tetradecanoylphorbol Acetate 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 24036252-3 2013 The ensuing Slug-dependent serine 139 phosphorylation of the DNA damage sensor H2AX in breast cancer stem cells induces tumor necrosis factor-alpha and IL-8 mRNAs, whose stability is enhanced by cytoplasmic beta-catenin. Serine 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 22183614-8 2013 For the first time, this study demonstrated that the poultry PM-induced IL-8 secretion by human lung epithelial cells was regulated by cPLA2 activation through ERK-mediated serine phosphorylation, suggesting a mechanism of airway inflammation among poultry farm workers. Serine 173-179 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 24045679-8 2013 RESULTS: Silibinin suppressed the growth of HMC-1 cells and also reduced the production and mRNA expression of pro-inflammatory cytokines such as TNF-alpha, IL-6, and IL-8. Silybin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 24072000-12 2013 Through the short-term impact of chlorine e6-PDI on IL-6 and IL-8 secretion, PDI may inhibit the inflammatory cascade in at least keratocyte cultures. Chlorine 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 23958972-1 2013 The immunotoxicity of the synthetic pyrethroid alpha-cypermethrin (alphaCYP) was assessed in 30 occupationally exposed greenhouse workers and 30 non-exposed controls by comparing plasma levels of IL-1beta, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12p70, TNF-alpha, TNF-beta and INF-gamma. cypermethrin 47-65 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 23934279-5 2013 H2O2 significantly reduced FP-induced GR nuclear localization (3.4+-0.51- vs. 5.7+-0.85-fold increase, P<0.05) and suppression of IL-1beta-induced CXCL8 (62.3+-2.3 vs. 85.1+-7.0%, P<0.05). Hydrogen Peroxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 150-155 23916117-7 2013 In cancer NAF samples (containing higher amounts of aluminium salts) we also found a significantly increased levels of pro-inflammatory cytokines (IL-1beta, IL-6, IL-12 p70, and TNF-alpha) and chemoattractant CC and CXC chemokines (IL-8, MIP-1alpha and MCP-1). aluminium salts 52-67 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 23871663-7 2013 RESULTS: RV-16 infection impaired dexamethasone-dependent (1) inhibition of IL-1beta-induced CXCL8 release, (2) induction of mitogen-activated protein kinase phosphatase 1 gene expression, and (3) binding of GR to GREs in airway epithelial cells. Dexamethasone 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 23871663-10 2013 In rhinovirus-infected cells the combination of JNK and IKK2 inhibitors totally restored dexamethasone suppression of CXCL8 release, induction of mitogen-activated protein kinase phosphatase 1 gene expression, and GRalpha nuclear translocation. Dexamethasone 89-102 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 24002221-0 2013 Pyocyanin from Pseudomonas induces IL-8 production through the PKC and NF-kappaB pathways in U937 cells. Pyocyanine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 23180322-8 2013 The initial serum CXCL8 levels were significantly associated with the HAQ-DI at the fourth year while the %VC of baseline tended to be negatively associated with HAQ-DI at the fourth year. haq-di 70-76 C-X-C motif chemokine ligand 8 Homo sapiens 18-23 23911868-4 2013 Although short poly I:C ( 1-1.5 kb) induced greater amounts of TNF-alpha, IL-8, and IFN-beta and a stronger antiviral response in myeloid cells, it was a poor inducer in fibroblasts. Poly I-C 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 24002221-3 2013 An increased release of interleukin-8 (IL-8), a potent neutrophil chemoattractant, in response to pyocyanin may contribute to the marked infiltration of neutrophils and subsequent neutrophil-mediated tissue damage observed in Pseudomonas-associated lung diseases. Pyocyanine 98-107 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 24002221-6 2013 It was found that pyocyanin increased IL-8 release and mRNA expression in differentiated U937 cells in a concentration- and time-dependent manner. Pyocyanine 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 24002221-7 2013 Calphostin C (Cal C), a protein kinase C (PKC) inhibitor, and pyrrolidine dithiocarbamate (PDTC) , an NF-kappaB inhibitor, blocked IL-8 expression in a concentration-dependent manner in pyocyanin-induced U937 cells. pyrrolidine dithiocarbamic acid 62-89 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 24002221-7 2013 Calphostin C (Cal C), a protein kinase C (PKC) inhibitor, and pyrrolidine dithiocarbamate (PDTC) , an NF-kappaB inhibitor, blocked IL-8 expression in a concentration-dependent manner in pyocyanin-induced U937 cells. pyrrolidine dithiocarbamic acid 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 24002221-7 2013 Calphostin C (Cal C), a protein kinase C (PKC) inhibitor, and pyrrolidine dithiocarbamate (PDTC) , an NF-kappaB inhibitor, blocked IL-8 expression in a concentration-dependent manner in pyocyanin-induced U937 cells. Pyocyanine 186-195 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 24002221-8 2013 We concluded that pyocyanin promotes IL-8 secretion and mRNA expression in a concentration- and time-dependent manner and furthermore, that the PKC and NF-kappaBeta signaling pathways may be involved in the expression of IL-8 in pyocyanin-infected PMA-differentiated U937 cells. Pyocyanine 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 24002221-8 2013 We concluded that pyocyanin promotes IL-8 secretion and mRNA expression in a concentration- and time-dependent manner and furthermore, that the PKC and NF-kappaBeta signaling pathways may be involved in the expression of IL-8 in pyocyanin-infected PMA-differentiated U937 cells. Pyocyanine 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 24002221-8 2013 We concluded that pyocyanin promotes IL-8 secretion and mRNA expression in a concentration- and time-dependent manner and furthermore, that the PKC and NF-kappaBeta signaling pathways may be involved in the expression of IL-8 in pyocyanin-infected PMA-differentiated U937 cells. Pyocyanine 229-238 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 23795990-7 2013 In BAL fluid, the amount of hyaluronan was positively correlated with the percentage of inflammatory cells and the amount of CXCL8. Hyaluronic Acid 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 125-130 24145180-0 2013 Level of TNF-related apoptosis-inducing-ligand and CXCL8 correlated with 2-[18F]Fluoro-2-deoxy-D-glucose uptake in anti-VEGF treated colon cancers. Fluorodeoxyglucose F18 73-104 C-X-C motif chemokine ligand 8 Homo sapiens 51-56 24168697-10 2013 The plant extract, compounds ursolic acid and myricitrin (commercially acquired) significantly inhibited the release of inflammatory cytokines IL 8 and TNF alpha by suppressing them by 74 - 99%. ursolic acid 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 24168697-10 2013 The plant extract, compounds ursolic acid and myricitrin (commercially acquired) significantly inhibited the release of inflammatory cytokines IL 8 and TNF alpha by suppressing them by 74 - 99%. myricitrin 46-56 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 24188201-9 2013 RESULTS: CS exposure decreased PPARgamma expression, as well as increased IL-8, LTB4 and TLR4 expression levels in bronchial epithelial cells in vivo and in vitro. Cesium 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24188201-10 2013 Moreover, PPARgamma ligands counteracted CS-induced airway inflammation by reducing IL-8 and LTB4 expression levels that are associated with TLR4 and nuclear factor-kappa B (NF-kappaB). Cesium 41-43 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 23978569-0 2013 Differential inhibition of signaling pathways by two new imidazo-pyrazoles molecules in fMLF-OMe- and IL8-stimulated human neutrophil. imidazopyrazole 57-74 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 24250750-0 2013 Primary 1,25-dihydroxyvitamin D3 response of the interleukin 8 gene cluster in human monocyte- and macrophage-like cells. Calcitriol 8-32 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 24205328-5 2013 GW843682X did not impact Pam3CSK4-induced IL-1beta and IL-8 or LPS-induced IL-1beta, but it down-regulated LPS-induced IL-8 significantly. 5-(5,6-dimethoxy-1H-benzimidazol-1-yl)-3-((2-(trifluoromethyl)benzyl)oxy)thiophene-2-carboxamide 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 23978569-2 2013 Compounds 3l and 3r, a new class of arylcarbamoyl-imidazo-pyrazoles derivatives, were described as the first example of compounds able to inhibit human neutrophil chemotaxis induced by both fMLF-OMe and IL8. arylcarbamoyl-imidazo-pyrazoles 36-67 C-X-C motif chemokine ligand 8 Homo sapiens 203-206 24041930-10 2013 Rivaroxaban and GB83 prevented upregulation of PARs, ICAM-1, LOX-1, IL-8, and activation of MAP kinases. Rivaroxaban 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 24146965-4 2013 After addition of calcium to cultured keratinocytes, the immunological responses induced by imiquimod, such as activation of NF-kappaB and induction of TNF-alpha and IL-8, were more rapid and stronger. Calcium 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 24041930-10 2013 Rivaroxaban and GB83 prevented upregulation of PARs, ICAM-1, LOX-1, IL-8, and activation of MAP kinases. gb83 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 23811328-4 2013 The results showed that, on acute or chronic exposure to arsenite, HBE cells over-expressed the pro-inflammatory cytokines, interleukin-6 (IL-6), interleukin-8 (IL-8), and interleukin-1beta (IL-1beta). arsenite 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 146-159 23811328-4 2013 The results showed that, on acute or chronic exposure to arsenite, HBE cells over-expressed the pro-inflammatory cytokines, interleukin-6 (IL-6), interleukin-8 (IL-8), and interleukin-1beta (IL-1beta). arsenite 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 23811328-6 2013 Moreover, IL-6 and IL-8 were essential for the malignant progression of arsenite-transformed HBE cells. arsenite 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 23981042-6 2013 Also, that APDs inhibited the production of LPS-stimulated macrophages IL-6 and IL-8 suggests that risperidone and clozapine may inhibit inflammation. Risperidone 99-110 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 24083094-8 2013 Only succinic acid resulted in a significant increase in interleukin-8 production by infected macrophages. Succinic Acid 5-18 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 23876538-12 2013 RESULT(S): With parthenolide pretreatment, TNF-alpha-induced IL-8 gene and protein expression in ESCs were diminished. parthenolide 16-28 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 23904051-1 2013 Hierarchical assembly of Ti(IV)/Sn(II)-doped SnO2 nanosheets along titanate nanowires serving as both sacrificial templates and a Ti(IV) source is demonstrated, using SnCl2 as a tin precursor and Sn(II) dopants and NaF as the morphology controlling agent. sn(ii) 32-38 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 23904051-1 2013 Hierarchical assembly of Ti(IV)/Sn(II)-doped SnO2 nanosheets along titanate nanowires serving as both sacrificial templates and a Ti(IV) source is demonstrated, using SnCl2 as a tin precursor and Sn(II) dopants and NaF as the morphology controlling agent. Tin(IV) oxide 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 24083678-8 2013 Sulindac sulfide also induced activation of the AP-1 transcription factor, which co-operated with NF-kappaB in up-regulating IL-8. sulindac sulfide 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 24409733-4 2013 The method was successfully employed in the toxic effect test of NaF, NaCl, KBr and NaBF4 on luciferase. Sodium tetrafluoroborate 84-89 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 25002916-11 2013 Deferoxamine significantly reduced cytotoxicity and IL-6 and IL-8 secretion whereas Polymyxin B did not. Deferoxamine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 24198747-13 2013 Taken together, our results suggest that BFT induced IL-8 secretion may occur by the following process: E-cadherin cleavage, disruption of cellular interactions, activation of the beta-catenin pathway and IL-8 expression. SCHEMBL13664687 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 23981042-6 2013 Also, that APDs inhibited the production of LPS-stimulated macrophages IL-6 and IL-8 suggests that risperidone and clozapine may inhibit inflammation. Clozapine 115-124 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 24772960-2 2013 The study was based on the hypothesis that poultry PM would induce the release of inflammatory cytokine interleukin-8 (IL-8) by respiratory epithelial cells under the upstream regulation by cytosolic phospholipase A2 (cPLA2) activation and subsequent formation of cyclooxygenase (COX)- and lipoxygenase (LOX)-catalyzed arachidonic acid (AA) metabolites (eicosanoids). Arachidonic Acid 319-335 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 24198747-4 2013 BFT induces E-cadherin cleavage, cell rounding, activation of the beta-catenin pathway and secretion of IL-8 in colonic epithelial cells. SCHEMBL13664687 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 24772960-2 2013 The study was based on the hypothesis that poultry PM would induce the release of inflammatory cytokine interleukin-8 (IL-8) by respiratory epithelial cells under the upstream regulation by cytosolic phospholipase A2 (cPLA2) activation and subsequent formation of cyclooxygenase (COX)- and lipoxygenase (LOX)-catalyzed arachidonic acid (AA) metabolites (eicosanoids). Arachidonic Acid 319-335 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 24772960-2 2013 The study was based on the hypothesis that poultry PM would induce the release of inflammatory cytokine interleukin-8 (IL-8) by respiratory epithelial cells under the upstream regulation by cytosolic phospholipase A2 (cPLA2) activation and subsequent formation of cyclooxygenase (COX)- and lipoxygenase (LOX)-catalyzed arachidonic acid (AA) metabolites (eicosanoids). Eicosanoids 354-365 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 24772960-2 2013 The study was based on the hypothesis that poultry PM would induce the release of inflammatory cytokine interleukin-8 (IL-8) by respiratory epithelial cells under the upstream regulation by cytosolic phospholipase A2 (cPLA2) activation and subsequent formation of cyclooxygenase (COX)- and lipoxygenase (LOX)-catalyzed arachidonic acid (AA) metabolites (eicosanoids). Eicosanoids 354-365 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 24772960-6 2013 Poultry PM also significantly induced release of IL-8 by the cells in a dose- and time-dependent manner, which was significantly attenuated by the calcium chelating agents, antioxidants and COX- and LOX-specific inhibitors. Calcium 147-154 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 24772960-7 2013 The current study for the first time revealed that the poultry PM-induced IL-8 release from the respiratory epithelial cells was regulated upstream by reactive oxygen species, cPLA2-, COX- and LOX-derived eicosanoid lipid signal mediators. Reactive Oxygen Species 151-174 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24772960-7 2013 The current study for the first time revealed that the poultry PM-induced IL-8 release from the respiratory epithelial cells was regulated upstream by reactive oxygen species, cPLA2-, COX- and LOX-derived eicosanoid lipid signal mediators. Eicosanoids 205-215 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24198747-8 2013 Prior studies have suggested that BFT induces IL-8 expression by inducing E-cadherin cleavage; cells that do not express E-cadherin do not secrete IL-8 in response to BFT. SCHEMBL13664687 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 24198747-11 2013 We also show that EDTA-mediated disruption of E-cadherin interactions without E-cadherin degradation was sufficient to induce IL-8 secretion. Edetic Acid 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 23575601-8 2013 Furthermore, dioscorin suppressed IL-8 secretion and reduced changes of adhesion molecule expressions in H(2)O(2)-injured A549 cells. dioscorin 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 24198747-12 2013 Finally, we determined that HT29/C1 cells treated with LiCl (beta-catenin activator) induced IL-8 secretion in a dose-dependent and time-dependent manner. Lithium Chloride 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 24198747-13 2013 Taken together, our results suggest that BFT induced IL-8 secretion may occur by the following process: E-cadherin cleavage, disruption of cellular interactions, activation of the beta-catenin pathway and IL-8 expression. SCHEMBL13664687 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 23793449-7 2013 In the propofol group, IL-6 and IL-8 were significantly increased at T3 compared to T1. Propofol 7-15 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 23594598-3 2013 BTH inhibited the release of some of the key psoriatic cytokines such as tumor necrosis factor alpha, IL-8, IL-6, and CCL27 through the downregulation of NF-kappaB in normal human keratinocytes. bth 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 23733596-9 2013 Results showed that supplementation with LC and Na2S reduced NF-kappaB phosphorylation and the secretion of TNF-alpha, MCP-1, IL-8, IL-1beta, and IP-10. sodium sulfide 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 23488973-6 2013 For PcP patients, BALF levels of IL-8, IL-8/IL-10 ratio and IL-8/TGF-beta1 ratio and blood levels of IL-8 and IL-8/IL-10 ratio were significantly higher in the patients with PaO2/FiO2 < 200 mmHg than in those with PaO2/FiO2 > 200 mmHg. pao2 174-178 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 23460381-12 2013 Because IL-8 induced an increase in EAA level, it is suggested that the EAA level reflects the primed state of polymorphonuclear leukocytes. ethyl acetoacetate 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 23799521-9 2013 There was a significant reduction in IL-8 concentration 24 hours after BMA associated with the concomitant administration of steroids and methotrexate. bma 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 23799521-9 2013 There was a significant reduction in IL-8 concentration 24 hours after BMA associated with the concomitant administration of steroids and methotrexate. Steroids 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 23799521-9 2013 There was a significant reduction in IL-8 concentration 24 hours after BMA associated with the concomitant administration of steroids and methotrexate. Methotrexate 138-150 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 23488973-6 2013 For PcP patients, BALF levels of IL-8, IL-8/IL-10 ratio and IL-8/TGF-beta1 ratio and blood levels of IL-8 and IL-8/IL-10 ratio were significantly higher in the patients with PaO2/FiO2 < 200 mmHg than in those with PaO2/FiO2 > 200 mmHg. pao2 174-178 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 23488973-6 2013 For PcP patients, BALF levels of IL-8, IL-8/IL-10 ratio and IL-8/TGF-beta1 ratio and blood levels of IL-8 and IL-8/IL-10 ratio were significantly higher in the patients with PaO2/FiO2 < 200 mmHg than in those with PaO2/FiO2 > 200 mmHg. pao2 174-178 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 23488973-6 2013 For PcP patients, BALF levels of IL-8, IL-8/IL-10 ratio and IL-8/TGF-beta1 ratio and blood levels of IL-8 and IL-8/IL-10 ratio were significantly higher in the patients with PaO2/FiO2 < 200 mmHg than in those with PaO2/FiO2 > 200 mmHg. pao2 174-178 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 24378059-9 2013 (3) The reduction of TNFalpha and IL-8 levels were positively correlated with reduction of NF-kappaB activity after intervention of rolipram in group B3 (r = 0.874, P < 0.01; r = 0.561, P < 0.05 respectively). Rolipram 132-140 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 23727622-1 2013 Chronic exposure to arsenic can generate reactive oxidative species, which can induce certain proinflammatory cytokines such as tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and interleukin-8 (IL-8). Arsenic 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 194-207 23727622-1 2013 Chronic exposure to arsenic can generate reactive oxidative species, which can induce certain proinflammatory cytokines such as tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6) and interleukin-8 (IL-8). Arsenic 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 23727622-10 2013 The present results also showed a significant increase in UC risk in subjects with the IL-8 -251 T/T genotype for each SD increase in urinary total arsenic and MMA%. Arsenic 148-155 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 23727622-11 2013 In contrast, a significant decrease in UC risk was found in subjects who carried the IL-8 -251 T/T genotype for each SD increase in DMA%. N-myristoyl-alaninol 132-135 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 23954527-7 2013 Montelukast treatment prevented IL-8 release and heterologous beta2-adrenoceptor desensitization in human BSMC exposed to monocyte-derived MPs by blocking NF-kappaB nuclear translocation. montelukast 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 23499888-7 2013 NHBE cells increased IL-8 production in a dose-dependent manner in response to CSC while DHBE cells did not show any significant difference and had a much lower production of IL-8 in response to CSC compared to NHBE cells. dhbe 89-93 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 23499888-11 2013 DHBE cells exhibit a dampened IL-8 release, indicating that COPD is associated with a reduced capacity of airway epithelial cells to respond to foreign material. dhbe 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 23969730-9 2013 Further experiments identified that ATP could promote IL-8 and Snail expression and inhibit E-cadherin and Claudin-1 expression. Adenosine Triphosphate 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 24223512-1 2013 The aim of this paper was to describe the in vitro effect of sodium fluoride (NaF) on the specific activity of the major erythrocyte antioxidant enzymes, as well as on the membrane malondialdehyde concentration, as indicators of oxidative stress. Sodium Fluoride 61-76 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 24223512-5 2013 The presence of vitamin E partially reversed the toxic effects of NaF on erythrocytes. Vitamin E 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 66-69 24223512-6 2013 These findings suggest that NaF induces oxidative stress in erythrocytes in vitro, and this stress is partially reversed by the presence of vitamin E. Vitamin E 140-149 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 23988269-0 2013 Direct determination of the NaF/AlF3 molar ratio by Raman spectroscopy in NaF-AlF3-CaF2 melts at 1000 C. For the last 40 years, Raman spectroscopy has been very useful in investigating the structure of corrosive molten salts, such as the cryolite-based melts widely used as electrolyte in the Hall-Heroult process. aluminum fluoride 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 24066150-7 2013 RESULTS: Roflumilast and Roflumilast-N-oxide concentration-dependently reduced the release of TNF-alpha and chemokines CCL2, CCL3, CCL4, CXCL9 and CXCL10 from LPS-stimulated human lung explants, whereas CXCL1, CXCL5 and CXCL8 release was not altered. roflumilast N-oxide 25-44 C-X-C motif chemokine ligand 8 Homo sapiens 220-225 24039842-5 2013 Our data showed that cyanidin-3-glucoside reduced cytokine-induced inflammation in intestinal cells, in terms of NO, PGE2 and IL-8 production and of iNOS and COX-2 expressions, at a much lower concentration than 5-aminosalicylic acid, suggesting a higher anti-inflammatory efficiency. cyanidin-3-o-glucoside 21-41 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 24049670-0 2013 The role of calcium, NF-kappaB and NFAT in the regulation of CXCL8 and IL-6 expression in Jurkat T-cells. Calcium 12-19 C-X-C motif chemokine ligand 8 Homo sapiens 61-66 24049670-6 2013 Interestingly, NF-kappaB activation by heat killed E. coli, as well as CXCL8 and IL-6 expression was significantly suppressed following addition of the calcium ionophore. Calcium 152-159 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 23448158-7 2013 In NaCl solution with 0.02 M NaF, NiTi suffer localized corrosion, while beta titanium alloys remained passive. nacl solution 3-16 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 23590581-4 2013 RESULTS: MgSO4 exposure increased intracellular magnesium levels, reducing the frequency of THP-1 cells producing IL-1beta, IL-8, and TNF-alpha following LPS stimulation. Magnesium Sulfate 9-14 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 23448158-11 2013 When 0.02 and 0.04 M of NaF were added to the NaCl solution, NiTi presented localized corrosion. nacl solution 46-59 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 23475935-9 2013 NTBI levels were higher after transfusion (p<0.01) returning to pretransfusion levels by 24 h. Post-transfusion NTBI level correlated with the age of transfused blood (p<0.001) and was positively correlated with plasma MDA (p=0.01) but not IL-1beta, IL-6, IL8 or TNFalpha. ntbi 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 262-265 23475935-9 2013 NTBI levels were higher after transfusion (p<0.01) returning to pretransfusion levels by 24 h. Post-transfusion NTBI level correlated with the age of transfused blood (p<0.001) and was positively correlated with plasma MDA (p=0.01) but not IL-1beta, IL-6, IL8 or TNFalpha. ntbi 115-119 C-X-C motif chemokine ligand 8 Homo sapiens 262-265 23845509-6 2013 Moreover, GTN down-regulated translocation of the p50/p65 heterodimer to the nucleus, prevented binding of NF-kappaB to its DNA response element and reduced TNF-alpha-activated interleukin-8 (IL-8) expression. goniothalamin 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 177-190 23578643-2 2013 Our results demonstrated that high glucose-induced oxidative stress in HUVECs was mainly mediated through activation of reactive oxygen species (ROS), Jun N-kinase 2/3 (JNK2/3) and plasma interleukin-8 (IL-8), and inactivation of phosphorylated protein kinase B (P-Akt). Glucose 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 188-201 23578643-2 2013 Our results demonstrated that high glucose-induced oxidative stress in HUVECs was mainly mediated through activation of reactive oxygen species (ROS), Jun N-kinase 2/3 (JNK2/3) and plasma interleukin-8 (IL-8), and inactivation of phosphorylated protein kinase B (P-Akt). Glucose 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 23578643-4 2013 Furthermore, 5-HMF rapidly inhibited high glucose-induced activation of IL-8, a downstream activator of P-Akt. Glucose 42-49 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 23845509-6 2013 Moreover, GTN down-regulated translocation of the p50/p65 heterodimer to the nucleus, prevented binding of NF-kappaB to its DNA response element and reduced TNF-alpha-activated interleukin-8 (IL-8) expression. goniothalamin 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 23900994-6 2013 In this review we summarise the ability of curcumin to interfere with signalling pathways Wnt, Hedgehog, Notch, Signal Transducers and Activator (STAT) and interleukin-8, and report curcumin-induced changes in function and properties of cancer stem cells. Curcumin 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 156-169 23751319-6 2013 Compared with the LPS control group, APS (100 mug/mL) or SAPS (100 mug/mL) administration decreased the expression of TNF-alpha, IL-1beta and IL-8. saps 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 23679817-0 2013 Inhibition by new glucocorticoid antedrugs [16alpha, 17alpha-d] isoxazoline and [16alpha, 17alpha-d]-3"-hydroxy-iminoformyl isoxazoline derivatives of chemotaxis and CCL26, CCL11, IL-8, and RANTES secretion. glucocorticoid antedrugs 18-42 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 23679817-0 2013 Inhibition by new glucocorticoid antedrugs [16alpha, 17alpha-d] isoxazoline and [16alpha, 17alpha-d]-3"-hydroxy-iminoformyl isoxazoline derivatives of chemotaxis and CCL26, CCL11, IL-8, and RANTES secretion. [16alpha, 17alpha-d] isoxazoline 43-75 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 23679817-0 2013 Inhibition by new glucocorticoid antedrugs [16alpha, 17alpha-d] isoxazoline and [16alpha, 17alpha-d]-3"-hydroxy-iminoformyl isoxazoline derivatives of chemotaxis and CCL26, CCL11, IL-8, and RANTES secretion. [16alpha, 17alpha-d]-3"-hydroxy-iminoformyl isoxazoline 80-135 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 23894194-0 2013 Proteasome inhibition by bortezomib increases IL-8 expression in androgen-independent prostate cancer cells: the role of IKKalpha. Bortezomib 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 23894194-4 2013 In this article, we report that proteasome inhibition by BZ unexpectedly increases IL-8 expression in androgen-independent prostate cancer PC3 and DU145 cells, whereas expression of other NF-kappaB-regulated genes is inhibited or unchanged. Bortezomib 57-59 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 23894194-5 2013 The BZ-increased IL-8 expression is associated with increased in vitro p65 NF-kappaB DNA binding activity and p65 recruitment to the endogenous IL-8 promoter. Bortezomib 4-6 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 23894194-5 2013 The BZ-increased IL-8 expression is associated with increased in vitro p65 NF-kappaB DNA binding activity and p65 recruitment to the endogenous IL-8 promoter. Bortezomib 4-6 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 23894194-6 2013 In addition, proteasome inhibition induces a nuclear accumulation of IkappaB kinase (IKK)alpha, and inhibition of IKKalpha enzymatic activity significantly attenuates the BZ-induced p65 recruitment to IL-8 promoter and IL-8 expression, demonstrating that the induced IL-8 expression is mediated, at least partly, by IKKalpha. Bortezomib 171-173 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 23894194-6 2013 In addition, proteasome inhibition induces a nuclear accumulation of IkappaB kinase (IKK)alpha, and inhibition of IKKalpha enzymatic activity significantly attenuates the BZ-induced p65 recruitment to IL-8 promoter and IL-8 expression, demonstrating that the induced IL-8 expression is mediated, at least partly, by IKKalpha. Bortezomib 171-173 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 23894194-6 2013 In addition, proteasome inhibition induces a nuclear accumulation of IkappaB kinase (IKK)alpha, and inhibition of IKKalpha enzymatic activity significantly attenuates the BZ-induced p65 recruitment to IL-8 promoter and IL-8 expression, demonstrating that the induced IL-8 expression is mediated, at least partly, by IKKalpha. Bortezomib 171-173 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 23894194-7 2013 Together, these data provide the first evidence, to our knowledge, for the gene-specific increase of IL-8 expression by proteasome inhibition in prostate cancer cells and suggest that targeting both IKKalpha and the proteasome may increase BZ effectiveness in treatment of androgen-independent prostate cancer. Bortezomib 240-242 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 23629852-7 2013 Cobalt increased secretion of IL8 and MCP1 significantly, and upregulated the expression of ICAM-1 in ECs compared to stimulation by chromium and controls. Cobalt 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 23661232-6 2013 Resveratrol significantly decreased both basal and interferon-gamma (IFN-gamma) (200 ng/ml)-stimulated levels of MCP-1, IL-6, and IL-8 and significantly attenuated both basal and IFN-gamma-stimulated activity of ERK. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 23661232-8 2013 Therefore, resveratrol is thought to inhibit production of MCP-1, IL-6, and IL-8 in HCASMCs through attenuating ERK activity. Resveratrol 11-22 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 23661232-0 2013 Inhibitory effects of resveratrol on MCP-1, IL-6, and IL-8 production in human coronary artery smooth muscle cells. Resveratrol 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 23661232-5 2013 Basal levels of monocyte chemoattractant protein-1 (MCP-1), interleukin (IL)-6, and IL-8 were significantly decreased in the presence of resveratrol at 1-50 muM in a concentration-dependent manner and were significantly decreased in the presence of U0126, an ERK inhibitor. Resveratrol 137-148 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 23890848-4 2013 RESULTS: A combination of EPA and DHA significantly reduced the concentration of IL-8 and IL-6 released into the supernatant compared to untreated controls (p<0.001). Eicosapentaenoic Acid 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 23765639-6 2013 METHODS: Evaluation of the effect of tadalafil and vardenafil on secretion of interleukin 8 (IL-8, a surrogate marker of prostate inflammation) by human myofibroblast prostatic cells (hBPH) exposed to different inflammatory stimuli. Vardenafil Dihydrochloride 51-61 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 23765639-8 2013 RESULTS: In vitro treatment with tadalafil or vardenafil on hBPH reduced IL-8 secretion induced by either TNFalpha or metabolic factors, including oxidized low-density lipoprotein, oxLDL, to the same extent as a PDE5-insensitive PKG agonist Sp-8-Br-PET-cGMP. Tadalafil 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 23765639-8 2013 RESULTS: In vitro treatment with tadalafil or vardenafil on hBPH reduced IL-8 secretion induced by either TNFalpha or metabolic factors, including oxidized low-density lipoprotein, oxLDL, to the same extent as a PDE5-insensitive PKG agonist Sp-8-Br-PET-cGMP. Vardenafil Dihydrochloride 46-56 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 24068928-6 2013 Furthermore, the UL76-mediated induction of IL-8 requires ATM and is correlated with the phosphorylation of NEMO on serine 85, indicating that UL76 activates NF-kB pathway by the DNA Damage response, similar to the impact of genotoxic drugs. Serine 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 23890848-4 2013 RESULTS: A combination of EPA and DHA significantly reduced the concentration of IL-8 and IL-6 released into the supernatant compared to untreated controls (p<0.001). Dihydroalprenolol 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 23890848-5 2013 Stimulation of PPARgamma with troglitazone reduced IL-8 production, and the PPARgamma antagonist GW9662 partially reversed this effect. Troglitazone 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 23792671-7 2013 The most remarkable gene induced by DON and 15ADON was inflammatory chemokine IL-8 and thus mRNA expression and secretion of IL-8 were analyzed by PCR and ELISA. deoxynivalenol 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 23792671-7 2013 The most remarkable gene induced by DON and 15ADON was inflammatory chemokine IL-8 and thus mRNA expression and secretion of IL-8 were analyzed by PCR and ELISA. deoxynivalenol 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 23792671-7 2013 The most remarkable gene induced by DON and 15ADON was inflammatory chemokine IL-8 and thus mRNA expression and secretion of IL-8 were analyzed by PCR and ELISA. 15-acetyldeoxynivalenol 44-50 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 24003340-14 2013 Although not fully evaluated in pNETs, biomarkers associated with response to sunitinib in several tumor types include soluble vascular endothelial growth factor receptor 2 and 3, interleukin 8, and stromal cell-derived factor 1alpha. Sunitinib 78-87 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 23792671-7 2013 The most remarkable gene induced by DON and 15ADON was inflammatory chemokine IL-8 and thus mRNA expression and secretion of IL-8 were analyzed by PCR and ELISA. 15-acetyldeoxynivalenol 44-50 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 23792671-8 2013 Both DON and acetylated DONs could induce mRNA expression and production of IL-8. deoxynivalenol 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 23792671-8 2013 Both DON and acetylated DONs could induce mRNA expression and production of IL-8. DONS 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 23792671-9 2013 In particular, ELISA assay showed that the ability to produce IL-8 was ranked as 3ADON<DON<15ADON. 15-acetyldeoxynivalenol 97-103 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 23792671-10 2013 Our results indicated that 15ADON caused the highest permeability and highest IL-8 secretion among DON, 3ADON, and 15ADON in human intestinal cell. 15-acetyldeoxynivalenol 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 23792671-10 2013 Our results indicated that 15ADON caused the highest permeability and highest IL-8 secretion among DON, 3ADON, and 15ADON in human intestinal cell. deoxynivalenol 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 23792671-10 2013 Our results indicated that 15ADON caused the highest permeability and highest IL-8 secretion among DON, 3ADON, and 15ADON in human intestinal cell. 3-acetyldeoxynivalenol 104-109 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 23766431-7 2013 RESULTS: Etidronate, at the lower concentration, significantly increased the expression of interleukin (IL)-6 (p=0.03) and IL-8 (p=0.04). Etidronic Acid 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 23991101-7 2013 This massive in vitro evidence supports the hypotheses that SMF-exposure (i) is harmful to lymphocytes in itself, (ii) suppresses the release of pro-inflammatory cytokines IL-6, IL-8, and TNF-alpha, and (iii) assists the production of anti-inflammatory cytokine IL-10; thus providing a background mechanism of the earlier in vivo demonstrated anti-inflammatory effects of SMF-exposure. smf 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 23831464-0 2013 Differential regulation of CC chemokine ligand 2 and CXCL8 by antifungal agent nystatin in macrophages. Nystatin 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 53-58 23831464-4 2013 However, nystatin dose-dependently increased CCL2 and CXCL8 expression at the mRNA and protein levels. Nystatin 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 54-59 23831464-5 2013 To understand the molecular mechanisms of the antifungal agent, we identified cellular factors activated by nystatin and those involved in nystatin-induced upregulation of CCL2 and CXCL8. Nystatin 139-147 C-X-C motif chemokine ligand 8 Homo sapiens 181-186 23831464-8 2013 Nystatin-mediated CXCL8 expression was attenuated in the presence of Akt inhibitor IV and SP6001250. Nystatin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 18-23 23831464-8 2013 Nystatin-mediated CXCL8 expression was attenuated in the presence of Akt inhibitor IV and SP6001250. sp6001250 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 18-23 23831464-9 2013 These results indicate that exposure of human macrophages to nystatin can lead to differential regulation of CCL2 and CXCL8 via the activation of multiple cellular kinases. Nystatin 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 23831464-10 2013 We propose that upregulation of CCL2 and CXCL8 contributes to pharmacological effects of nystatin. Nystatin 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 41-46 23865744-0 2013 Influence of sodium halides (NaF, NaCl, NaBr, NaI) on the photocatalytic performance of hydrothermally synthesized hematite photoanodes. hematite photoanodes 115-135 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 23865744-3 2013 In this study, we prepared hematite photoanodes hydrothermally from precursor solutions of 0.1 M FeCl3 at pH 1.55 with a background electrolyte of 1.0 M sodium halide (NaF, NaCl, NaBr, or NaI). hematite photoanodes 27-47 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 24062615-7 2013 RESULTS: We have demonstrated that budesonide concentration-dependently (10(-10)-10(-7) M) inhibited IL-6, IL-8, MMP-1, and MMP-3 release by HFL-1 cells in response to IL-1beta plus TNF-alpha. Budesonide 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23977231-6 2013 Inhibition studies using antisense RNA and the pharmacological agent BAY-117082 confirmed the involvement of NF-kappaB in IL-6, IL-8, and IL-1beta secretion. 3-(4-methylphenylsulfonyl)-2-propenenitrile 69-79 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 23977237-6 2013 Furthermore, ATROSAB inhibited release of IL-6 and IL-8 from HeLa and HT1080 cells, respectively, induced by TNF or lymphotoxin alpha (LTalpha). atrosab 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 23578198-2 2013 Our present study revealed that sunitinib-treated RCC cells exhibit senescence characteristics including increased SA-beta-gal activity, DcR2 and Dec1 expression, and senescence-associated secretary phenotype (SASP) such as proinflammatory cytokines interleukin (IL)-1alpha, IL-6 and IL-8 secretion. Sunitinib 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 284-288 23766431-9 2013 Alendronate, at the highest concentration, significantly increased the expression of IL-8 (p=0.02) and decreased the expression of eotaxin (p=0.02). Alendronate 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 22354777-0 2013 Phosphorylation of histone H3 at serine 10 has an essential role in arsenite-induced expression of FOS, EGR1 and IL8 mRNA in cultured human cell lines. arsenite 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 23930605-10 2013 Pre-clinical trials have shown vitamin D to not only decrease BPH cell and prostate cell proliferation alone, but also when induced by known growth promoting molecules such as IL-8, Des (1-3) IGF-1, testosterone and dihydrotestosterone. Vitamin D 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 23607720-8 2013 In neutrophils, 15-epi-LXA4 showed a moderate reduction of interleukin (IL)-8-mediated neutrophil chemotaxis but no effect on neutrophil survival was observed. lipoxin A4 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 59-77 23607720-10 2013 In conclusion, 15-epi-LXA4 is not a functional agonist or an antagonist of FPR2/ALX or CysLT1, shows no effect on IL-8-induced neutrophil survival and produces only moderate inhibition in IL-8-mediated neutrophil migration. lipoxin A4 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 23590633-9 2013 In HMC-1 cells, [6]-shogaol inhibited the production of TNF-alpha, IL-6 and IL-8, as well as the activation of nuclear factor-kappaB (NF-kappaB) and phosphorylation of JNK in compound 48/80-induced HMC-1 cells. shogaol 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 22354777-0 2013 Phosphorylation of histone H3 at serine 10 has an essential role in arsenite-induced expression of FOS, EGR1 and IL8 mRNA in cultured human cell lines. Serine 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 23649946-5 2013 We review studies showing a relationship between elevated aqueous VEGF, monocyte chemoattractant protein -1, interleukin 6, or interleukin 8 in association with DME and as predictors of DME. dme 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 23794083-9 2013 Using this technique, we have measured changes in LJPs for diluted solutions of NaCl, LiCl, KCl, CsCl and NaF, obtaining excellent agreement within +-0.1 mV of predicted values, calculated using ion activities. ljps 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 23794083-10 2013 Our de novo LJP measurements of biionic combinations of the above undiluted salts, and NaI and NaF (with halide anions I- and F-), generally also gave excellent agreement with predicted values. halide 105-111 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 23456484-5 2013 We also found that although dexamethasone suppressed the release of these two cytokines, mast cells recruitment, and mucus hypersecretion, it actually increased neutrophil infiltration and the level of keratinocyte-derived chemokine (mKC), a functional homolog of human IL-8. Dexamethasone 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 270-274 23456484-7 2013 The elevated IL-8 level was suppressed by BAY11-7082, a selective NF-kappaB inhibitor, but not by dexamethasone. 3-(4-methylphenylsulfonyl)-2-propenenitrile 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 23456484-8 2013 These results suggest that increased IL-8 (mKC) levels may be involved in steroid-resistant neutrophilic airway inflammation through an NF-kappaB-dependent pathway. Steroids 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 22354777-6 2013 U0126 treatment significantly reduced constitutive mRNA expression of FOS and EGR1, and dramatically suppressed the induction of FOS, EGR1 and IL8 mRNA in iAs(III)-treated cells. U 0126 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 143-146 22354777-8 2013 When the histone H3 nonphosphorylatable mutant of serine 10 (S10A) was overexpressed in cells, iAs(III) induction of FOS, EGR1and IL8 expression was significantly decreased as compared with wild-type cells. Serine 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 23817417-7 2013 Combined celecoxib and TNF-alpha blockade more effectively suppressed the proinflammatory loop than did single treatment, as shown by lower IL-6, IL-8, matrix metalloproteinase-1 and matrix metalloproteinase-3 production. Celecoxib 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 23779254-5 2013 The pharmacologic inhibitors of ERK, U0126 and PD98059, effectively reduced IL-8 expression and the active forms of ERK signaling molecules, as detected by anti-phosphorylated p44/42 antibody. U 0126 37-42 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 23779254-5 2013 The pharmacologic inhibitors of ERK, U0126 and PD98059, effectively reduced IL-8 expression and the active forms of ERK signaling molecules, as detected by anti-phosphorylated p44/42 antibody. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 47-54 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 24051972-5 2013 RESULTS: After six months of DHA supplementation inflammatory marker levels had diminished: interleukin 8 (IL-8) and Tumour Necrosis Factor Alfa (TNF-alpha) in serum, and calprotectin in stools. dehydroacetic acid 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 23720457-10 2013 IL-8 release induced by S-LPS, which requires CD14 to activate TLR4, was blocked by bosentan and BQ788. Bosentan 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23720457-10 2013 IL-8 release induced by S-LPS, which requires CD14 to activate TLR4, was blocked by bosentan and BQ788. BQ 788 97-102 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23712703-4 2013 However, the receptor for advanced glycation end products (RAGE) blocker RAGE-Ab (5 mug/ml) or 10 muM c-Jun N-terminal kinases (JNK) inhibitor SP600125 could inhibit HMGB1-induced the release of inflammation cytokines including TNF-alpha, IL-8, IL-10, and MCP-1 in a dose-dependent manner. pyrazolanthrone 143-151 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 24051972-5 2013 RESULTS: After six months of DHA supplementation inflammatory marker levels had diminished: interleukin 8 (IL-8) and Tumour Necrosis Factor Alfa (TNF-alpha) in serum, and calprotectin in stools. dehydroacetic acid 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23936340-3 2013 To identify inhibitors of the NOD2 signaling pathway, we utilized a cell-based screening approach and identified a benzimidazole diamide compound designated GSK669 that selectively inhibited an MDP-stimulated, NOD2-mediated IL-8 response without directly inhibiting RIP2 kinase activity. benzimidazole diamide 115-136 C-X-C motif chemokine ligand 8 Homo sapiens 224-228 23764888-5 2013 Arazyme inhibited the secretion of IL-6 and IL-8 due to phorbol 12-myristate 13-acetate and calcium ionophores in human mast cells. Tetradecanoylphorbol Acetate 56-87 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 23764888-5 2013 Arazyme inhibited the secretion of IL-6 and IL-8 due to phorbol 12-myristate 13-acetate and calcium ionophores in human mast cells. Calcium 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 24303127-5 2013 Tulobuterol reduced the RV14 titers and RNA levels; the concentrations of cytokines, including interleukin (IL)-1beta, IL-6, and IL-8, in the supernatants; and susceptibility to RV14 infection. tulobuterol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 23784034-14 2013 HCl exposure increased the levels of IL-8 and the release of LDH, and induced apoptosis in BEAS-2B cells. Hydrochloric Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 23189959-4 2013 Lactate production, glucose uptake and the percentage of oocytes reaching metaphase II decreased in a dose-dependent manner in the presence of the pharmacological (NaF) or the physiological (ATP) inhibitors of glycolysis (p < 0.05). Lactic Acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 164-167 23936340-3 2013 To identify inhibitors of the NOD2 signaling pathway, we utilized a cell-based screening approach and identified a benzimidazole diamide compound designated GSK669 that selectively inhibited an MDP-stimulated, NOD2-mediated IL-8 response without directly inhibiting RIP2 kinase activity. gsk669 157-163 C-X-C motif chemokine ligand 8 Homo sapiens 224-228 23526216-0 2013 Role of hypoxia-inducible factor 1, alpha subunit and cAMP-response element binding protein 1 in synergistic release of interleukin 8 by prostaglandin E2 and nickel in lung fibroblasts. Dinoprostone 137-153 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 23578767-6 2013 Increased IL-8 secretion required HMC-fibroblast intercellular contact, was enhanced by serum and was blocked by the gap junction inhibitor beta-glycyrrhetinic. beta-glycyrrhetinic 140-159 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 23578767-8 2013 IL-8 secretion by fibroblasts was strongly promoted by hyaluronic acid. Hyaluronic Acid 55-70 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23578767-9 2013 Pre-treatment of HMC with thapsigargin provoked 15-fold higher IL-8 production by fibroblasts in co-cultures. Thapsigargin 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 23403077-8 2013 The growth of the tumor spheres could also be reduced by the CXCR2 specific inhibitor SB225002 or the PI3K/AKT inhibitor LY294002, indicating that the endogenously produced CXCL8 plays an autocrine role in the growth of the tumor spheres. SB 225002 86-94 C-X-C motif chemokine ligand 8 Homo sapiens 173-178 23403077-8 2013 The growth of the tumor spheres could also be reduced by the CXCR2 specific inhibitor SB225002 or the PI3K/AKT inhibitor LY294002, indicating that the endogenously produced CXCL8 plays an autocrine role in the growth of the tumor spheres. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 173-178 23403077-9 2013 Further mechanistic studies revealed that the gene expression of CXCL8 could be reduced by the MIF specific small interfering RNA (siRNA) or NF-kappaB inhibitor parthenolide, and the growth of tumor spheres was also reduced after MIF siRNA transfection. parthenolide 161-173 C-X-C motif chemokine ligand 8 Homo sapiens 65-70 23844176-2 2013 Nickel compounds are well established human carcinogens, however, little is known about the influence of nickel on the spontaneous secretion of IL-8 in oral squamous cell carcinoma (OSCC) cells. Nickel 105-111 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 23844176-3 2013 The aim of the present study was to investigate whether Ni(2+) ions can influence on IL-8 secretion by OSCC. Nickel(2+) 56-62 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 23844176-11 2013 Our results demonstrated that, on the contrary to our expectations, Ni(2+) ions inhibited the spontaneous secretion of IL-8. Nickel(2+) 68-74 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 23844176-12 2013 As IL-8 reduction was observed in a transcriptional level, we performed the luciferase assay and the data indicated that Ni(2+) ions reduced the NF-kappaB activity. Nickel(2+) 121-127 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 23895055-7 2013 Using HUVECs we demonstrated that tylophorine inhibited VEGF-stimulated inflammatory responses including IL-6, IL-8, TNF-alpha, IFN-gamma, MMP-2 and NO secretion. tylophorine 34-45 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 23770363-0 2013 Vitamin D upregulates glutamate cysteine ligase and glutathione reductase, and GSH formation, and decreases ROS and MCP-1 and IL-8 secretion in high-glucose exposed U937 monocytes. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 23770363-7 2013 1,25 (OH)2 vitamin D caused significantly (p<0.05) lower secretion of IL-8 and MCP-1, and lower ROS levels in monocytes exposed to control and HG-treated monocytes. 1,25 (oh)2 vitamin d 0-20 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 23874538-2 2013 Lung epithelial cell released IL-8 plays a crucial role in CS induced lung inflammation. Cesium 59-61 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 23874538-3 2013 CS and cigarette smoke extracts (CSE) both induce IL-8 secretion and subsequently, IL-8 recruits inflammatory cells into the lung parenchyma. Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 23874538-3 2013 CS and cigarette smoke extracts (CSE) both induce IL-8 secretion and subsequently, IL-8 recruits inflammatory cells into the lung parenchyma. Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 23742030-12 2013 Microdialysis levels of histamine, IL-6 and IL-8 assessed 1-3 h after cold challenge were significantly (P < 0.05) decreased following up-dosing with 80 mg bilastine. bilastine 159-168 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 23526216-0 2013 Role of hypoxia-inducible factor 1, alpha subunit and cAMP-response element binding protein 1 in synergistic release of interleukin 8 by prostaglandin E2 and nickel in lung fibroblasts. Nickel 158-164 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 23526216-3 2013 The current study sought to identify the molecular events underlying Ni-induced alterations in PGE2 signaling and its effects on IL-8 production. Dinoprostone 95-99 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 23526216-4 2013 PGE2 synergistically enhances Ni-induced IL-8 release from HLF in a concentration-dependent manner. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 23883807-10 2013 Nine of 14 patients in the FF group (64%) reported slight to total relief of nasal symptoms, and this subgroup had a significant decrease in IL-8 levels in nasal secretions after 6 weeks of treatment (850.7 +- 207.2 pg/mL versus 1608 +- 696.5 pg/mL; p = 0.03) compared with baseline. fluticasone furoate 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 23526216-6 2013 PGE2 and forskolin stimulated cAMP, but it was only in the presence of Ni-induced hypoxia-inducible factor 1, alpha subunit (HIF1A) that these agents stimulated IL-8 release. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 23526216-6 2013 PGE2 and forskolin stimulated cAMP, but it was only in the presence of Ni-induced hypoxia-inducible factor 1, alpha subunit (HIF1A) that these agents stimulated IL-8 release. Colforsin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 23603753-8 2013 Rebamipide also suppressed TNFalpha-induced expression of interleukin-6 and interleukin-8 at the mRNA and protein levels and inhibited the TNFalpha-induced degradation of IkappaBalpha. rebamipide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 23583258-3 2013 This report concerns the marked up-regulation in differentiated CaCo-2 colonic epithelial cells of two key inflammatory interleukins, IL-6 and IL-8, caused by a mixture of oxysterols representative of a high cholesterol diet. Oxysterols 172-182 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 23583258-3 2013 This report concerns the marked up-regulation in differentiated CaCo-2 colonic epithelial cells of two key inflammatory interleukins, IL-6 and IL-8, caused by a mixture of oxysterols representative of a high cholesterol diet. Cholesterol 208-219 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 24174716-3 2013 These bacterial species initiate the production of various cytokines such as interleukin-8 and TNF-alpha, further causing an increase in number and activity of polymorphonucleocytes (PMN) along with these cytokines, PMNs also produce reactive oxygen species (ROS) superoxide via the respiratory burst mechanism as the part of the defence response to infection. Reactive Oxygen Species 234-257 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 23683858-4 2013 ppTGRL were found to increase the secretion of chemoattractants, including monocyte chemoattractant protein-1 (MCP-1), macrophage inflammatory protein (MIP)-1alpha and -1beta and IL-8, by HMDM and to have a stimulatory effect on monocyte chemotaxis. pptgrl 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 23628225-6 2013 The BALF concentrations of IL-1beta; IL-8; interferon-gamma-induced protein 10; regulated upon activation, normal T-cell expressed and secreted; neutrophil elastase; and pepsin were higher in patients with BOS (p < 0.05). N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 206-209 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 23564008-0 2013 The concentrations of IL-8 and IL-6 in gingival crevicular fluid during nickel-chromium alloy porcelain crown restoration. Nickel 72-78 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 23564008-0 2013 The concentrations of IL-8 and IL-6 in gingival crevicular fluid during nickel-chromium alloy porcelain crown restoration. Chromium 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 23758162-3 2013 EXPERIMENTAL APPROACH: Corticosteroid sensitivity was determined by IC50/EC50 of dexamethasone (Dex) on TNF-alpha-induced CXCL8 production in U937 monocytic cell line and peripheral blood mononuclear cells (PBMC) from COPD patients. Dexamethasone 81-94 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 23758162-3 2013 EXPERIMENTAL APPROACH: Corticosteroid sensitivity was determined by IC50/EC50 of dexamethasone (Dex) on TNF-alpha-induced CXCL8 production in U937 monocytic cell line and peripheral blood mononuclear cells (PBMC) from COPD patients. Dexamethasone 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 122-127 23211751-5 2013 Furthermore, adrenaline significantly reduced the expression of chemokine CXCL8_L1 (a functional homolog of mammalian IL-8) and its receptors (CXCR1 and CXCR2), indicating changes in leukocyte recruitment after stress. Epinephrine 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 23564008-1 2013 We explored gum irritation and cytotoxicity caused by nickel-chromium (Ni-Cr) alloy porcelain by interleukin-8 (IL-8), interleukin-6 (IL-6) and gingival crevicular fluid (GCF) volumes at different time points peri-crown restoration. nichrome 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 24174716-3 2013 These bacterial species initiate the production of various cytokines such as interleukin-8 and TNF-alpha, further causing an increase in number and activity of polymorphonucleocytes (PMN) along with these cytokines, PMNs also produce reactive oxygen species (ROS) superoxide via the respiratory burst mechanism as the part of the defence response to infection. Reactive Oxygen Species 259-262 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 23564008-1 2013 We explored gum irritation and cytotoxicity caused by nickel-chromium (Ni-Cr) alloy porcelain by interleukin-8 (IL-8), interleukin-6 (IL-6) and gingival crevicular fluid (GCF) volumes at different time points peri-crown restoration. nichrome 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 23564008-5 2013 The total amount and concentrations of IL-8 and IL-6 per site, GCF volumes increased after nickel-chromium (Ni-Cr) alloy-porcelain crown restoration, and reached its peak at the third month as the GCF volume increased by 52.20 %, the total amount and concentrations of IL-8 increased by 112.11 and 22.75 %; the total amount and concentrations of IL-6 increased by 77.66 and 17.17 % when compared to baseline. nichrome 91-106 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 24174716-3 2013 These bacterial species initiate the production of various cytokines such as interleukin-8 and TNF-alpha, further causing an increase in number and activity of polymorphonucleocytes (PMN) along with these cytokines, PMNs also produce reactive oxygen species (ROS) superoxide via the respiratory burst mechanism as the part of the defence response to infection. Superoxides 264-274 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 23564008-5 2013 The total amount and concentrations of IL-8 and IL-6 per site, GCF volumes increased after nickel-chromium (Ni-Cr) alloy-porcelain crown restoration, and reached its peak at the third month as the GCF volume increased by 52.20 %, the total amount and concentrations of IL-8 increased by 112.11 and 22.75 %; the total amount and concentrations of IL-6 increased by 77.66 and 17.17 % when compared to baseline. nichrome 108-113 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 23748240-0 2013 Repression of miR-143 mediates Cr (VI)-induced tumor angiogenesis via IGF-IR/IRS1/ERK/IL-8 pathway. chromium hexavalent ion 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 23564008-7 2013 The increase in the total amount and the concentrations of IL-8 and IL-6 and GCF volume may be related to the cytotoxicity induced by Ni-Cr alloy. nichrome 134-139 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 23564008-8 2013 The significant increase of IL-8 concentration in females indicates that more attention should be given to women during Ni-Cr alloy porcelain crown restoration. nichrome 120-125 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 23629517-4 2013 Results indicate that robust changes in the expression of the proinflammatory cytokine interleukin 8 (IL8) and the vascular cell adhesion molecule 1 (VCAM1) occur within 5h of exposure to CAS. cas 188-191 C-X-C motif chemokine ligand 8 Homo sapiens 87-100 23629517-4 2013 Results indicate that robust changes in the expression of the proinflammatory cytokine interleukin 8 (IL8) and the vascular cell adhesion molecule 1 (VCAM1) occur within 5h of exposure to CAS. cas 188-191 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 23475986-8 2013 Although naringenin significantly attenuated IL-1beta-induced IL-6 and IL-8 mRNA expression and release, there was no effect of curcumin and apigenin. naringenin 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 22899541-3 2013 In concentrations of 5 muM-20 muM, PGG demonstrated statistically significant inhibition of ROS generation, IL-8 secretion and beta2 integrin expression in stimulated neutrophils. pgg 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 23617551-10 2013 Inhaled budesonide significantly reduced LPS-induced IL-1beta, IL-6, IL-8 and TNF-alpha secretion, while inhaled formoterol had no such effect; however when combined, the inhibitory effect of budesonide was significantly increased by formoterol. Budesonide 8-18 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 23629517-6 2013 Analysis shows that CAS induced the release of IL8 and IL6. cas 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 23791132-7 2013 In VTE patients atorvastatin decreased IL-6 (p=0.0003), IL-8 (p=0.003) and P-selectin (p<0.0001), but increased IL-10 (p=0.001), with no association with C-reactive protein or cholesterol-lowering effects. Atorvastatin 16-28 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 23680662-5 2013 Here we report that a KS disaccharide, [SO3(-)-6]Galbeta1-4[SO3(-)-6]GlcNAc, designated as L4, suppressed the production of Interleukin-8 (IL-8) stimulated by flagellin, a Toll-like receptor (TLR) 5 agonist, in normal human bronchial epithelial (NHBE) cells. ks disaccharide 22-37 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 23774942-0 2013 A soft coral natural product, 11-episinulariolide acetate, inhibits gene expression of cyclooxygenase-2 and interleukin-8 through attenuation of calcium signaling. 11-episinulariolide acetate 30-57 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 23774942-0 2013 A soft coral natural product, 11-episinulariolide acetate, inhibits gene expression of cyclooxygenase-2 and interleukin-8 through attenuation of calcium signaling. Calcium 145-152 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 23680662-5 2013 Here we report that a KS disaccharide, [SO3(-)-6]Galbeta1-4[SO3(-)-6]GlcNAc, designated as L4, suppressed the production of Interleukin-8 (IL-8) stimulated by flagellin, a Toll-like receptor (TLR) 5 agonist, in normal human bronchial epithelial (NHBE) cells. ks disaccharide 22-37 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 23680662-5 2013 Here we report that a KS disaccharide, [SO3(-)-6]Galbeta1-4[SO3(-)-6]GlcNAc, designated as L4, suppressed the production of Interleukin-8 (IL-8) stimulated by flagellin, a Toll-like receptor (TLR) 5 agonist, in normal human bronchial epithelial (NHBE) cells. [so3(-)-6]galbeta1-4[so3(-)-6]glcnac 39-75 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 23611835-1 2013 SB225002 (SB) is an IL-8 receptor B (IL-8RB) antagonist that has previously been shown to inhibit IL-8-based cancer cell invasion, and to possess in vivo anti-inflammatory and anti-nociceptive effects. SB 225002 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 23611835-1 2013 SB225002 (SB) is an IL-8 receptor B (IL-8RB) antagonist that has previously been shown to inhibit IL-8-based cancer cell invasion, and to possess in vivo anti-inflammatory and anti-nociceptive effects. SB 225002 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 23611835-10 2013 In summary, the present study introduced SB as a promising antitumor agent which has the potential to exert its activity through dual mechanisms involving microtubules targeting and interference with IL-8-drivin cancer progression. SB 225002 41-43 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 23578390-1 2013 Sodium fluoride (NaF) is widely used for the treatment of dental caries and dentin hypersensitivity. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 23578390-5 2013 Exposure of cells to 4mM NaF for 24h induced caspase-3 activation, ultrastructural alterations, and resulted in the translocation of Bax to the mitochondria and the release of cytochrome c from the mitochondrial inter-membrane space into the cytosol, indicating that fluoride-mediated apoptosis is mitochondria-dependent. Fluorides 267-275 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 23680662-5 2013 Here we report that a KS disaccharide, [SO3(-)-6]Galbeta1-4[SO3(-)-6]GlcNAc, designated as L4, suppressed the production of Interleukin-8 (IL-8) stimulated by flagellin, a Toll-like receptor (TLR) 5 agonist, in normal human bronchial epithelial (NHBE) cells. [so3(-)-6]galbeta1-4[so3(-)-6]glcnac 39-75 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 23740581-8 2013 RESULTS: The levels of IL-8 and TNF-alpha in EBC, the levels of exhaled NO, and the percentage of neutrophils in induced sputum were significantly elevated in C and B compared with A; the EBC pH level was significantly reduced in C and B compared with A. NSC638702 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 23740581-9 2013 The EBC levels of IL-8, TNF-alpha, pH, the level of exhaled NO, and the percentage of neutrophils correlated significantly with age. NSC638702 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 23600826-7 2013 Similarly, co-incubation of fatty acids with glucose diminished secretion of IL-10, IFN-gamma and CCL2 (monocyte chemotactic protein-1), while IL-8 was up-regulated (P < 0 001). Fatty Acids 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 23161900-11 2013 Finally, DAPT significantly decreased VEGF/Ang2 induced IL-6, IL-8, MMP2 and 9 expressions in RA synovial explants. dapt 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 23602068-9 2013 Methylprednisolone significantly lowered concentrations of proinflammatory cytokines IL-6 and IL-8 and raised levels of anti-inflammatory IL-10. Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 23633491-6 2013 Together these findings offer a rationale for dual inhibition of IL-6/IL-8 signaling as a therapeutic strategy to improve outcomes for patients with TNBCs. tnbcs 149-154 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 23885223-6 2013 Therefore, these results provide immunological information about amorphous silica nanoparticles and suggest that amorphous silica nanoparticles can evoke innate immune reactions in human monocytes through production of IL-1beta and IL-8. Silicon Dioxide 123-129 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 23605466-6 2013 More recently, another molecular probe 18 F-sodium fluoride (18 F-NaF) was introduced for PET imaging, which targets active microcalcifications in atherosclerotic plaques. Sodium Fluoride 43-59 C-X-C motif chemokine ligand 8 Homo sapiens 66-69 23602200-7 2013 Only ROS generation was highly affected by the blockade of PMN-secreted TNF-alpha or IL-8. Reactive Oxygen Species 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 23199585-7 2013 CAM and AZM induced a dose-dependent suppression of spontaneous TNF-alpha, sTNFR2, IL-6, IL-8 and CCL18 production (p<0.05). Clarithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 23199585-7 2013 CAM and AZM induced a dose-dependent suppression of spontaneous TNF-alpha, sTNFR2, IL-6, IL-8 and CCL18 production (p<0.05). Azithromycin 8-11 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 23199585-9 2013 CAM and AZM significantly and dose-dependently attenuated the LPS-stimulated production of sTNFR1, sTNFR2, IL-8 and CCL18 (p<0.05). Clarithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23199585-9 2013 CAM and AZM significantly and dose-dependently attenuated the LPS-stimulated production of sTNFR1, sTNFR2, IL-8 and CCL18 (p<0.05). Azithromycin 8-11 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23659606-3 2013 Results obtained by scanning electron microscopy (SEM) and SEM/energy dispersive X-ray analyses proved that the hydroxyapatite and bioactive glass-containing toothpastes were highly efficient in promoting enamel remineralization by formation of deposits and a protective layer on the surface of the demineralized enamel, whereas the toothpaste containing 8% strontium acetate and 1040 ppm fluoride as NaF had little, if any, remineralization potential. Durapatite 112-126 C-X-C motif chemokine ligand 8 Homo sapiens 401-404 23588209-9 2013 TES inhibited UVB-induced production of the pro-inflammatory cytokines interleukin (IL)-6 and IL-8 in a dose-dependent manner. tectroside 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 23588209-10 2013 In addition, TES inhibited the expression of cyclooxygenase (COX)-2 and the phosphorylation of c-Jun NH2-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) MAPKs, suggesting that it inhibits the secretion of the pro-inflammatory cytokines IL-6 and IL-8 and COX-2 expression by blocking MAPK phosphorylation. tectroside 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 267-271 23862231-6 2013 CONCLUSION: The levels of IL-8 and COX-2 in EPS indirectly reflect those in the prostate tissue. eps 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 23620238-11 2013 Co-treatment with DHT significantly inhibited oxLDL-induced secretion of IL-8, whilst an AR-antagonist, bicalutamide, reversed DHT effects. Dihydrotestosterone 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 23274767-8 2013 However, the activity of the cationic nanoparticles on the IL-8 promoter and NF-kappaB translocation is lost when cholesterol is depleted from A549 cells before particle exposure, which suggests that cationic nanoparticles rely on membrane cholesterol integrity to disrupt cellular signaling. Cholesterol 114-125 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 23274767-8 2013 However, the activity of the cationic nanoparticles on the IL-8 promoter and NF-kappaB translocation is lost when cholesterol is depleted from A549 cells before particle exposure, which suggests that cationic nanoparticles rely on membrane cholesterol integrity to disrupt cellular signaling. Cholesterol 240-251 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 23458894-0 2013 Crotonaldehyde-exposed macrophages induce IL-8 release from airway epithelial cells through NF-kappaB and AP-1 pathways. 2-butenal 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 23458896-1 2013 We have previously observed that 1-nitropyrene (1-NP) and its amine metabolite 1-aminopyrene (1-AP) induce differential chemokine responses in human bronchial epithelial cells (BEAS-2B) characterized by maximum responses for CXCL8 (IL-8) and CCL5 (RANTES), respectively. 1-nitropyrene 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 225-230 23458896-1 2013 We have previously observed that 1-nitropyrene (1-NP) and its amine metabolite 1-aminopyrene (1-AP) induce differential chemokine responses in human bronchial epithelial cells (BEAS-2B) characterized by maximum responses for CXCL8 (IL-8) and CCL5 (RANTES), respectively. 1-nitropyrene 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 23458896-1 2013 We have previously observed that 1-nitropyrene (1-NP) and its amine metabolite 1-aminopyrene (1-AP) induce differential chemokine responses in human bronchial epithelial cells (BEAS-2B) characterized by maximum responses for CXCL8 (IL-8) and CCL5 (RANTES), respectively. 1-nitropyrene 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 225-230 23458896-1 2013 We have previously observed that 1-nitropyrene (1-NP) and its amine metabolite 1-aminopyrene (1-AP) induce differential chemokine responses in human bronchial epithelial cells (BEAS-2B) characterized by maximum responses for CXCL8 (IL-8) and CCL5 (RANTES), respectively. 1-nitropyrene 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 23458896-1 2013 We have previously observed that 1-nitropyrene (1-NP) and its amine metabolite 1-aminopyrene (1-AP) induce differential chemokine responses in human bronchial epithelial cells (BEAS-2B) characterized by maximum responses for CXCL8 (IL-8) and CCL5 (RANTES), respectively. 1-aminopyrene 79-92 C-X-C motif chemokine ligand 8 Homo sapiens 225-230 23458896-1 2013 We have previously observed that 1-nitropyrene (1-NP) and its amine metabolite 1-aminopyrene (1-AP) induce differential chemokine responses in human bronchial epithelial cells (BEAS-2B) characterized by maximum responses for CXCL8 (IL-8) and CCL5 (RANTES), respectively. 1-aminopyrene 79-92 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 23458896-1 2013 We have previously observed that 1-nitropyrene (1-NP) and its amine metabolite 1-aminopyrene (1-AP) induce differential chemokine responses in human bronchial epithelial cells (BEAS-2B) characterized by maximum responses for CXCL8 (IL-8) and CCL5 (RANTES), respectively. 1-aminopyrene 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 225-230 23458896-1 2013 We have previously observed that 1-nitropyrene (1-NP) and its amine metabolite 1-aminopyrene (1-AP) induce differential chemokine responses in human bronchial epithelial cells (BEAS-2B) characterized by maximum responses for CXCL8 (IL-8) and CCL5 (RANTES), respectively. 1-aminopyrene 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 23458896-4 2013 However, at a low concentration (1 muM) where neither 1-NP, 1-AP nor unsubstituted pyrene had any effect on chemokine responses, we found that all three PAHs potentiated CXCL8 and CCL5 responses induced by the TLR3 ligand polyinosinic:polycytidylic acid (Poly I:C) in BEAS-2B cells. Polycyclic Aromatic Hydrocarbons 153-157 C-X-C motif chemokine ligand 8 Homo sapiens 170-175 23632478-8 2013 CONCLUSION: Lenalidomide favours a uniform TNF-alpha and IL-8 inflammatory and IGF-1 secretory profile of myeloma cells, an observation that raises important questions for therapeutic approaches incorporating the agent. Lenalidomide 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 23458894-7 2013 Furthermore, BEAS-2B and A549 cells directly treated with crotonaldehyde induced increase in IL-8 production. 2-butenal 58-72 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 23458894-8 2013 These data suggest that crotonaldehyde is capable of directly stimulating the production of IL-8 in both macrophages and airway epithelial cells. 2-butenal 24-38 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 23458894-9 2013 Crotonaldehyde-stimulated macrophages also amplify the inflammatory response by enhancing IL-8 release from airway epithelial cells mediated by NF-kappaB and AP-1 pathways through a mechanism involving TNF-alpha and IL-1beta. 2-butenal 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 23443656-5 2013 We also demonstrate that TgMIF can elicit IL-8 production from human peripheral blood mononuclear cells while also activating ERK MAPK pathways in murine bone marrow-derived macrophages. tgmif 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 22915623-7 2013 RESULTS: Simvastatin decreased IL-17-induced IL-6, IL-8, CX3CL-1, RANTES mRNA and CX3CL-1 and CCL20 production. Simvastatin 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 23007230-0 2013 Paediatric acute generalized exanthematous pustulosis induced by paracetamol with high serum levels of interleukin-8 and -22: a case report. Acetaminophen 65-76 C-X-C motif chemokine ligand 8 Homo sapiens 103-124 23357535-4 2013 Thrombin-induced increases in IL-8/CXCL8 release and kappaB-luciferase activity were inhibited by the Shc small interfering RNA (siRNA), p66Shc siRNA, GW 5074 (a Raf-1 inhibitor), and PD98059 (a mitogen-activated protein kinase (MAPK) kinase (MEK) inhibitor). 5-iodo-3-((3,5-dibromo-4-hydroxyphenyl)methylene)-2-indolinone 151-158 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 23357535-4 2013 Thrombin-induced increases in IL-8/CXCL8 release and kappaB-luciferase activity were inhibited by the Shc small interfering RNA (siRNA), p66Shc siRNA, GW 5074 (a Raf-1 inhibitor), and PD98059 (a mitogen-activated protein kinase (MAPK) kinase (MEK) inhibitor). 5-iodo-3-((3,5-dibromo-4-hydroxyphenyl)methylene)-2-indolinone 151-158 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 23357535-4 2013 Thrombin-induced increases in IL-8/CXCL8 release and kappaB-luciferase activity were inhibited by the Shc small interfering RNA (siRNA), p66Shc siRNA, GW 5074 (a Raf-1 inhibitor), and PD98059 (a mitogen-activated protein kinase (MAPK) kinase (MEK) inhibitor). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 184-191 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 23425072-0 2013 Acidic deoxycholic acid and chenodeoxycholic acid induce interleukin-8 production through p38 mitogen-activated protein kinase and protein kinase A in a squamous epithelial model. Deoxycholic Acid 7-23 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 23186593-5 2013 The levels of IL-6, IL-8 and ICAM were significantly lower in the GL group. gl 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 23554253-4 2013 Whereas the reactive oxygen species production and IL-6 secretion were similar following a 24-h treatment with either MC, 100 microM MC-LR induced a five-fold greater IL-8 secretion when compared to MC-RR. cyanoginosin LR 133-138 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 22995323-8 2013 In subjects receiving SB-656933 50mg, sputum neutrophils and elastase were reduced compared to baseline (probability of a true reduction, 0.889 and 0.882 respectively), and free DNA reduced compared to placebo (probability of a true reduction, 0.967), while blood levels of fibrinogen, CRP and CXCL8 were increased. SB 656933 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 294-299 23525265-8 2013 The PCN (100 mumol/L) significantly increased the production of interleukin-8 (IL-8), prostaglandin E2 (PGE2), and leukotriene B4 (LTB4) in both cell lines. Pyocyanine 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 64-77 23525265-8 2013 The PCN (100 mumol/L) significantly increased the production of interleukin-8 (IL-8), prostaglandin E2 (PGE2), and leukotriene B4 (LTB4) in both cell lines. Pyocyanine 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 23525265-9 2013 Consistent with its paradoxical role in modulating PCN-induced toxicity, 3-MA (5 mmol/L) significantly reduced the PCN-induced production of IL-8, PGE2, and LTB4 in 1321N1 astrocytoma cells but augmented their production in SH-SY5Y neuroblastoma cells. 3-methyladenine 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 23525265-9 2013 Consistent with its paradoxical role in modulating PCN-induced toxicity, 3-MA (5 mmol/L) significantly reduced the PCN-induced production of IL-8, PGE2, and LTB4 in 1321N1 astrocytoma cells but augmented their production in SH-SY5Y neuroblastoma cells. Pyocyanine 115-118 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 23525265-10 2013 In conclusion, we show here for the first time the paradoxical role of autophagy in mediating PCN-induced toxicity in 1321N1 astrocytoma and SH-SY5Y neuroblastoma cells and provide novel evidence that these actions may be mediated by effects on IL-8, PGE2, and LTB4 production. Pyocyanine 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 23611390-5 2013 METHODS: Endodontic files were dissolved in sodium fluoride (NaF) by passing a 50-mA current through the NiTi files while immersed in the NaF solution. Sodium Fluoride 44-59 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 23611390-9 2013 RESULTS: NaF solution reduced PDL cell survival, and the NaF/NiTi solution further reduced PDL cell survival. nitinol 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 23425072-0 2013 Acidic deoxycholic acid and chenodeoxycholic acid induce interleukin-8 production through p38 mitogen-activated protein kinase and protein kinase A in a squamous epithelial model. Chenodeoxycholic Acid 28-49 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 23425072-2 2013 The effects of bile acids, which are major components of reflux fluid, on the production of IL-8 and related mechanisms remain unclear. Bile Acids and Salts 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 23425072-5 2013 Bile acids under different pH conditions were added to the apical compartment to examine their effects on IL-8 production and the underlying cellular signaling. Bile Acids and Salts 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 23425072-6 2013 RESULTS: Conjugated bile acids under a neutral or acidic condition did not induce IL-8 production, and unconjugated bile acids, deoxycholic acid (DCA), and chenodeoxycholic acid (CDCA) all significantly induced IL-8 production, dose- and time-dependently, only under weakly acid conditions. Chenodeoxycholic Acid 156-177 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 23425072-7 2013 Inhibition of p38 mitogen-activated protein kinase (p38 MAPK) and protein kinase A (PKA) attenuated the production of IL-8 induced by acidic DCA and CDCA. Deoxycholic Acid 141-144 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 23425072-7 2013 Inhibition of p38 mitogen-activated protein kinase (p38 MAPK) and protein kinase A (PKA) attenuated the production of IL-8 induced by acidic DCA and CDCA. Chenodeoxycholic Acid 149-153 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 23425072-9 2013 CONCLUSIONS: Compared with conjugated bile acids, the unconjugated bile acids DCA and CDCA are more likely to induce IL-8 production in vivo, especially under weakly acid conditions. Bile Acids and Salts 67-77 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 23425072-9 2013 CONCLUSIONS: Compared with conjugated bile acids, the unconjugated bile acids DCA and CDCA are more likely to induce IL-8 production in vivo, especially under weakly acid conditions. Deoxycholic Acid 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 23425072-9 2013 CONCLUSIONS: Compared with conjugated bile acids, the unconjugated bile acids DCA and CDCA are more likely to induce IL-8 production in vivo, especially under weakly acid conditions. Chenodeoxycholic Acid 86-90 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 23386688-9 2013 Using pharmacological inhibition of NF-kappaB and inducible knockdown of NF-kappaB p65, we found that JSI-124-induced expression of IL-6, IL-8, and SOCS3 was significantly inhibited, showing an NF-kappaB-dependent mechanism. jsi 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 23047422-5 2013 Morphine and methadone, but not fentanyl, at >10(-5) M decreased all tested cytokines except IL-8. Morphine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 23047422-5 2013 Morphine and methadone, but not fentanyl, at >10(-5) M decreased all tested cytokines except IL-8. Methadone 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 23488692-9 2013 Furthermore, NS-398 reduced the production of IL-6 and IL-8, thus indicating that IL-1beta/HMGB1 complexes modulate cytokine production in part through prostanoid synthesis. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 23384547-5 2013 METHODS: The effect of sodium fluoride (NaF) on glycolytic metabolism of cultured chondrocytes was confirmed by measurement of intracellular adenosine triphosphate (ATP) production. Sodium Fluoride 23-38 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 23384547-5 2013 METHODS: The effect of sodium fluoride (NaF) on glycolytic metabolism of cultured chondrocytes was confirmed by measurement of intracellular adenosine triphosphate (ATP) production. Adenosine Triphosphate 141-163 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 23384547-5 2013 METHODS: The effect of sodium fluoride (NaF) on glycolytic metabolism of cultured chondrocytes was confirmed by measurement of intracellular adenosine triphosphate (ATP) production. Adenosine Triphosphate 165-168 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 23384547-8 2013 RESULTS: ATP production was dose-dependently decreased by NaF in the human chondrocytic cell line HCS-2/8. Adenosine Triphosphate 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 23384547-12 2013 CONCLUSIONS: These findings suggest that decreased ATP production by NaF promotes hypertrophy-like changes via activation of phospho-Smad1/5/8 in the presence of lactate. Adenosine Triphosphate 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 23384547-12 2013 CONCLUSIONS: These findings suggest that decreased ATP production by NaF promotes hypertrophy-like changes via activation of phospho-Smad1/5/8 in the presence of lactate. Lactic Acid 162-169 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 23488692-9 2013 Furthermore, NS-398 reduced the production of IL-6 and IL-8, thus indicating that IL-1beta/HMGB1 complexes modulate cytokine production in part through prostanoid synthesis. Prostaglandins 152-162 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 23613823-0 2013 Enterococcus faecalis inhibits superantigen toxic shock syndrome toxin-1-induced interleukin-8 from human vaginal epithelial cells through tetramic acids. tetramic acid 139-153 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 23613823-7 2013 We further demonstrated that this organism secretes two tetramic acid compounds which appear responsible for inhibition of interleukin-8 production, as well as inhibition of T cell proliferation due to toxic shock syndrome toxin-1. tetramic acid 56-69 C-X-C motif chemokine ligand 8 Homo sapiens 123-136 23454444-5 2013 KEY FINDINGS: alpha-Chaconine and solanidine significantly reduced interleukin-2 (IL-2) and interleukin-8 (IL-8) productions in Con A-induced Jurkat cells. alpha-chaconine 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 23454444-5 2013 KEY FINDINGS: alpha-Chaconine and solanidine significantly reduced interleukin-2 (IL-2) and interleukin-8 (IL-8) productions in Con A-induced Jurkat cells. alpha-chaconine 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23454444-5 2013 KEY FINDINGS: alpha-Chaconine and solanidine significantly reduced interleukin-2 (IL-2) and interleukin-8 (IL-8) productions in Con A-induced Jurkat cells. solanidine 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 23454444-5 2013 KEY FINDINGS: alpha-Chaconine and solanidine significantly reduced interleukin-2 (IL-2) and interleukin-8 (IL-8) productions in Con A-induced Jurkat cells. solanidine 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23616769-8 2013 EGCG inhibited interleukin (IL)-1beta, transforming growth factor beta, IL-8, and chemokine (C-C motif) ligand 2 (CCL2) release by stimulated FLS and/or THP-1 cells in a dose-dependent manner. epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 23616769-11 2013 Furthermore, MbetaCD enhanced the inflammatory response to CPP crystals increasing IL-8 and CCL2 secretion which was inhibited by EGCG in a dose-dependent manner. methyl-beta-cyclodextrin 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 23616769-11 2013 Furthermore, MbetaCD enhanced the inflammatory response to CPP crystals increasing IL-8 and CCL2 secretion which was inhibited by EGCG in a dose-dependent manner. epigallocatechin gallate 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 23369216-6 2013 Interestingly, our microarray and proteomics analysis show that only phenanthroline induced high expression and secretion of another angiogenic cytokine, interleukin-8, suggesting that the mechanism of phenanthroline-induced hypoxia is distinct from DFO and hypoxia and involves the activation of other signaling pathways. Phenanthrolines 69-83 C-X-C motif chemokine ligand 8 Homo sapiens 154-167 23449982-6 2013 Both the potential ligands and 6-OAU elicited chemotaxis of human polymorphonuclear leukocytes (PMNs) and macrophages and amplified LPS-stimulated production of the proinflammatory cytokine IL-8 from PMNs and TNFalpha from macrophages. 6-OAU 31-36 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 23557437-8 2013 A release of pro-inflammatory markers TNF-alpha and IL-8 was neither observed upon Ag-NP and AgNO3 exposures as well as was not affected when cells were pre-stimulated with lipopolysaccharide (LPS). Silver Nitrate 93-98 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 23557437-9 2013 Also, an induction of mRNA expression of TNF-alpha and IL-8, could only be observed for the highest AgNO3 concentration alone or even significantly increased when pre-stimulated with LPS after 4 h. However, this effect disappeared after 24 h. Furthermore, oxidative stress markers (HMOX-1, SOD-1) were expressed after 4 h in a concentration dependent manner following AgNO3 exposures only. Silver Nitrate 100-105 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 23557437-9 2013 Also, an induction of mRNA expression of TNF-alpha and IL-8, could only be observed for the highest AgNO3 concentration alone or even significantly increased when pre-stimulated with LPS after 4 h. However, this effect disappeared after 24 h. Furthermore, oxidative stress markers (HMOX-1, SOD-1) were expressed after 4 h in a concentration dependent manner following AgNO3 exposures only. Silver Nitrate 368-373 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 23481185-5 2013 RESULTS: Mono-methyl XAA analogues with substitutions at the seventh and eighth positions were the most active in stimulating human leukocytes to produce IL-6 and IL-8; and for inhibition of tube formation by ECV304 human endothelial-like cells, while 5- and 6-substituted analogues were the most active in murine cell systems. mono-methyl xaa 9-24 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 23083515-0 2013 Vitamin D inhibits the expression of interleukin-8 in human periodontal ligament cells stimulated with Porphyromonas gingivalis. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 23083515-2 2013 The present study aimed to discover the effects of 1a,25-dihydroxyvitamin D3 (1,25D) on the expressions of interleukin (IL)-6 and IL-8 in human periodontal ligament cells (hPDLCs) stimulated with Porphyromonas gingivalis (P. gingivalis) W83. Calcitriol 51-76 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 23083515-10 2013 CONCLUSION: Vitamin D may potentially inhibit the periodontal inflammation induced by P. gingivalis partly by decreasing the IL-8 expression in hPDLCs. Vitamin D 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 23488631-3 2013 SI, AD, and DM reduced a mean phorbol-12-myristate-13-acetate/ionomycin (PMA/I)-stimulated release of the pro-inflammatory interleukins IL-6 and IL-8 by more than 50% (p < 0.05). ad 4-6 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 23488631-3 2013 SI, AD, and DM reduced a mean phorbol-12-myristate-13-acetate/ionomycin (PMA/I)-stimulated release of the pro-inflammatory interleukins IL-6 and IL-8 by more than 50% (p < 0.05). Tetradecanoylphorbol Acetate 30-61 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 23488631-3 2013 SI, AD, and DM reduced a mean phorbol-12-myristate-13-acetate/ionomycin (PMA/I)-stimulated release of the pro-inflammatory interleukins IL-6 and IL-8 by more than 50% (p < 0.05). Ionomycin 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 23488631-5 2013 A significant, more than 50% mean inhibition of PMA/I-induced IL-6 and IL-8 release was demonstrated for the volatile compounds 1,8-cineole, borneol, camphor, and thujone, but not for the nonvolatile rosmarinic acid when applied in concentrations representative of sage infusion. Eucalyptol 128-139 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 23488631-5 2013 A significant, more than 50% mean inhibition of PMA/I-induced IL-6 and IL-8 release was demonstrated for the volatile compounds 1,8-cineole, borneol, camphor, and thujone, but not for the nonvolatile rosmarinic acid when applied in concentrations representative of sage infusion. isoborneol 141-148 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 23488631-5 2013 A significant, more than 50% mean inhibition of PMA/I-induced IL-6 and IL-8 release was demonstrated for the volatile compounds 1,8-cineole, borneol, camphor, and thujone, but not for the nonvolatile rosmarinic acid when applied in concentrations representative of sage infusion. Camphor 150-157 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 23488631-5 2013 A significant, more than 50% mean inhibition of PMA/I-induced IL-6 and IL-8 release was demonstrated for the volatile compounds 1,8-cineole, borneol, camphor, and thujone, but not for the nonvolatile rosmarinic acid when applied in concentrations representative of sage infusion. beta-thujone 163-170 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 23488631-5 2013 A significant, more than 50% mean inhibition of PMA/I-induced IL-6 and IL-8 release was demonstrated for the volatile compounds 1,8-cineole, borneol, camphor, and thujone, but not for the nonvolatile rosmarinic acid when applied in concentrations representative of sage infusion. rosmarinic acid 200-215 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 23472833-6 2013 We show that the salts when ordered by heat effects produced by mixing of NaF and NaBr with 3,3-, 6,9-, or 6,12-ionene fluorides and bromides follow the opposite ordering than in the case when the same alkali halide salts are mixed with more hydrophobic 12,12-ionene salts. 3,3-, 6,9-, or 6,12-ionene fluorides 92-128 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 23472833-6 2013 We show that the salts when ordered by heat effects produced by mixing of NaF and NaBr with 3,3-, 6,9-, or 6,12-ionene fluorides and bromides follow the opposite ordering than in the case when the same alkali halide salts are mixed with more hydrophobic 12,12-ionene salts. Bromides 133-141 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 23472833-6 2013 We show that the salts when ordered by heat effects produced by mixing of NaF and NaBr with 3,3-, 6,9-, or 6,12-ionene fluorides and bromides follow the opposite ordering than in the case when the same alkali halide salts are mixed with more hydrophobic 12,12-ionene salts. halide salts 209-221 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 23472833-6 2013 We show that the salts when ordered by heat effects produced by mixing of NaF and NaBr with 3,3-, 6,9-, or 6,12-ionene fluorides and bromides follow the opposite ordering than in the case when the same alkali halide salts are mixed with more hydrophobic 12,12-ionene salts. 12,12-ionene salts 254-272 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 23369216-6 2013 Interestingly, our microarray and proteomics analysis show that only phenanthroline induced high expression and secretion of another angiogenic cytokine, interleukin-8, suggesting that the mechanism of phenanthroline-induced hypoxia is distinct from DFO and hypoxia and involves the activation of other signaling pathways. Phenanthrolines 202-216 C-X-C motif chemokine ligand 8 Homo sapiens 154-167 23369216-6 2013 Interestingly, our microarray and proteomics analysis show that only phenanthroline induced high expression and secretion of another angiogenic cytokine, interleukin-8, suggesting that the mechanism of phenanthroline-induced hypoxia is distinct from DFO and hypoxia and involves the activation of other signaling pathways. dfo 250-253 C-X-C motif chemokine ligand 8 Homo sapiens 154-167 23295714-8 2013 RESULTS: Sevoflurane suppressed TNF-alpha-induced IL-6, IL-8, and MCP-1 gene expression and the production of IL-6 and IL-8 in SAEC under anoxia/reoxygenation conditions. Sevoflurane 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 23086737-1 2013 The aims of this study were to assess the effects and potential mechanisms of parthenolide on the expression of vascular endothelial growth factor (VEGF), interleukin 8 (IL-8) and matrix metalloproteinase 9 (MMP-9) in human breast cancer cell line MDA-MB-231. parthenolide 78-90 C-X-C motif chemokine ligand 8 Homo sapiens 155-168 23295714-8 2013 RESULTS: Sevoflurane suppressed TNF-alpha-induced IL-6, IL-8, and MCP-1 gene expression and the production of IL-6 and IL-8 in SAEC under anoxia/reoxygenation conditions. Sevoflurane 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 23295714-12 2013 CONCLUSIONS: Sevoflurane suppressed the NF-kappaB-mediated production of pulmonary epithelial cell-derived inflammatory cytokines, including IL-6 and IL-8, which are capable of causing I/R injury. Sevoflurane 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 23347208-6 2013 Our results showed that higher expression of interleukin-8 (IL-8) expression associated with 54.26 +- 34.46% of TAM infiltration of peritoneum was significantly higher than 16.58 +- 17.74% of CD3(+) T-cell by immunofluorescence co-staining and confocal microscopy. tam 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 23347208-6 2013 Our results showed that higher expression of interleukin-8 (IL-8) expression associated with 54.26 +- 34.46% of TAM infiltration of peritoneum was significantly higher than 16.58 +- 17.74% of CD3(+) T-cell by immunofluorescence co-staining and confocal microscopy. tam 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 23347208-7 2013 THP-1 cells exhibited M2-polarized phenotype markers with high proportion of CD68(+) , CD206(+) and CD204(+) markers after phorbol 12-myristate 13-acetate (PMA) treatment, After co-culturing with TAM cells in a transwell chamber system, EOC cells (SKOV3) increased their IL-8 expression at the level of mRNA and protein. Tetradecanoylphorbol Acetate 156-159 C-X-C motif chemokine ligand 8 Homo sapiens 271-275 23347208-9 2013 Furthermore, the upregulation of IL-8 expression in ovarian cancer cells induced by macrophages could be inhibited by pyrollidine dithiocarbamate, an inhibitor of nuclear factor (NF)- kappaB signal pathway. pyrollidine dithiocarbamate 118-145 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 23525981-0 2013 Retraction note: Late phase activation of nuclear transcription factor kappaB by doxorubicin is mediated by interleukin-8 and induction of apoptosis via FasL. Doxorubicin 81-92 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 23086737-1 2013 The aims of this study were to assess the effects and potential mechanisms of parthenolide on the expression of vascular endothelial growth factor (VEGF), interleukin 8 (IL-8) and matrix metalloproteinase 9 (MMP-9) in human breast cancer cell line MDA-MB-231. parthenolide 78-90 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 23086737-5 2013 The real-time PCR and Western blot data showed that the expressions of VEGF, IL-8 and MMP-9 were significantly inhibited by parthenolide at both transcription level and protein level in MDA-MB-231 cells. parthenolide 124-136 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 23086737-8 2013 Hence, the expression of VEGF, IL-8 and MMP-9 may be suppressed by parthenolide through the inhibition of NF-kappaB DNA-binding activity in MDA-MB-231 cells. parthenolide 67-79 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 23345392-0 2013 Sphingosine-1-phosphate suppresses TLR-induced CXCL8 secretion from human T cells. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 47-52 23498057-0 2013 Glutamine and alanine-induced differential expression of intracellular IL-6, IL-8, and TNF-alpha in LPS-stimulated monocytes in human whole-blood. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 23498057-0 2013 Glutamine and alanine-induced differential expression of intracellular IL-6, IL-8, and TNF-alpha in LPS-stimulated monocytes in human whole-blood. Alanine 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 23480345-7 2013 In particular, remifentanil decreased activation of intracellular signaling pathways, including p38 and ERK1/2, and expression of pro-inflammatory cytokines, including TNF-alpha, IL-6 and IL-8. Remifentanil 15-27 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 22727544-8 2013 Taurolidine inhibited immunoglobulin (IL)-6, IL-8 and tumor necrosis factor-alpha expression in a dose dependent-fashion in both, pediatric oncology patients and healthy controls. taurolidine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 45-81 23211566-10 2013 Unfractionated heparin significantly suppressed the TNF-alpha-induced and NF-kappaB-mediated secretion and expression of IL-8 and -6 as well as other molecules in decidualized and undifferentiated human ESCs. Heparin 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 121-132 22107042-1 2013 When resorbable hydroxyapatite (HA) granules, which are used as a bone supplement material, were treated in neutral 4% sodium fluoride (NaF) solution, formation of a reactant resembling calcium fluoride was observed on the surface of the granules. Durapatite 16-30 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 22107042-1 2013 When resorbable hydroxyapatite (HA) granules, which are used as a bone supplement material, were treated in neutral 4% sodium fluoride (NaF) solution, formation of a reactant resembling calcium fluoride was observed on the surface of the granules. Durapatite 32-34 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 22107042-1 2013 When resorbable hydroxyapatite (HA) granules, which are used as a bone supplement material, were treated in neutral 4% sodium fluoride (NaF) solution, formation of a reactant resembling calcium fluoride was observed on the surface of the granules. Sodium Fluoride 119-134 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 22107042-1 2013 When resorbable hydroxyapatite (HA) granules, which are used as a bone supplement material, were treated in neutral 4% sodium fluoride (NaF) solution, formation of a reactant resembling calcium fluoride was observed on the surface of the granules. Calcium Fluoride 186-202 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 22107042-7 2013 The promotion of MG-63 cell migration and proliferation, as well as increased ALP activity, suggested that fluoride released from the surface of resorbable HA granules, which were fluoridated by prior treatment with neutral 4% NaF solution, can provide a superb method to supply fluoride and promote osteogenic cell differentiation. Fluorides 107-115 C-X-C motif chemokine ligand 8 Homo sapiens 227-230 26105926-15 2013 IL-8 was inhibited up to 67% by the liposomal curcumin in human vaginal cell lines (End1/E6E7, Ect1/E6E7, VK2/E6E7) as compared to curcumin. Curcumin 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23276728-6 2013 CS inhibited NF-kappaB activation and the release of some of the key psoriatic cytokines such as TNFalpha, IL-8, IL-6 and CCL27. Chondroitin Sulfates 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 24627774-10 2013 Conversely, pretreatment with anacardic acid inhibited IL-8 production and expression in A549 cells. anacardic acid 30-44 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 23257347-8 2013 Compared to Placebo, treatment with Bimosiamose led to a decrease of the interleukin-8 concentration (-9.49 ng/mL, 95%CI -18.8 to -2.7 ng/mL, p = 0.008), for the neutrophil count a difference of -0.368 x 10(6) cells/mL (95%CI -1.256 to 0.407 x 10(6)/mL, p = 0.313) was found. bimosiamose 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 23434371-2 2013 However, here we show that Fas/CD95-induced apoptosis is associated with the production of an array of cytokines and chemokines, including IL-6, IL-8, CXCL1, MCP-1, and GMCSF. ammonium ferrous sulfate 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 23434371-3 2013 Fas-induced production of MCP-1 and IL-8 promoted chemotaxis of phagocytes toward apoptotic cells, suggesting that these factors serve as "find-me" signals in this context. ammonium ferrous sulfate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 23404123-9 2013 In B3 cells, the level of IL-8 increased significantly when the cells made direct contact with TA particles (1.33 times that of PBS, P < 0.05, Student"s t-test), but not in noncontact cultures. Triamcinolone Acetonide 95-97 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 23404123-9 2013 In B3 cells, the level of IL-8 increased significantly when the cells made direct contact with TA particles (1.33 times that of PBS, P < 0.05, Student"s t-test), but not in noncontact cultures. Lead 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 23433769-9 2013 Significant changes (defined a priori as p < 0.1) in favour of AZD9668 were also seen in slow vital capacity, plasma interleukin-8, and post-waking sputum interleukin-6 and Regulated on Activation, Normal T-cell Expressed and Secreted levels. N-((5-(methanesulfonyl)pyridin-2-yl)methyl)-6-methyl-5-(1-methyl-1H-pyrazol-5-yl)-2-oxo-1-(3-(trifluoromethyl)phenyl)-1,2-dihydropyridine-3-carboxamide 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 23481492-10 2013 Carvedilol could also preserve cardiac contractility via modulation of the tumor necrosis factor alpha and interleukin 8 mRNA expression and reduction of Bcl-2 and cytochrome c protein production and decrease the occurrence of apoptosis ex vivo. Carvedilol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 107-120 23859389-11 2013 CONCLUSION: Inhalation and intravenous infusion of ketamine before OLV are equally effective in lowering the serum levels of IL-6, IL-8 and sICAM-1. Ketamine 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 24627774-0 2013 Anacardic acid, a histone acetyltransferase inhibitor, modulates LPS-induced IL-8 expression in a human alveolar epithelial cell line A549. anacardic acid 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 24627774-9 2013 Pretreatment with TSA showed a dose-dependent stimulatory effect on IL-8 release from A549 cells as compared to LPS alone. trichostatin A 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 23292117-9 2013 Additionally, 50 and 100 mumol/L of EGCG significantly reduced the secretion of VEGF and IL-8 proteins induced by HPV-16 E7 oncoprotein in NSCLC A549 cells. epigallocatechin gallate 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 23356456-6 2013 Our analysis indicates that several BAL parameters, including neutrophil count, interleukin-8, alpha defensins and MMP-9, demonstrate highly replicable associations with BOS. N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 170-173 C-X-C motif chemokine ligand 8 Homo sapiens 80-93 23292117-12 2013 CONCLUSIONS: EGCG inhibited HPV-16 oncoprotein-induced angiogenesis conferred by NSCLC through the inhibition of HIF-1alpha protein expression and HIF-1alpha-dependent expression of VEGF, IL-8, and CD31 as well as activation of Akt, suggesting that HIF-1alpha may be a potential target of EGCG against HPV-related NSCLC angiogenesis. epigallocatechin gallate 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 23348104-1 2013 1-nitropyrene (1-NP), a common PAH in diesel exhaust, and its amine metabolite 1-aminopyrene (1-AP) induce distinctly different chemokine-responses in bronchial epithelial cells (BEAS-2B) characterized by increases in CXCL8 and CCL5, respectively. 1-nitropyrene 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 218-223 23466865-5 2013 Cyanidin, quercetin and PSPLE also significantly attenuated VCAM-1, IL-8 and CD40 expression, and quercetin significantly attenuated ICAM-1 and E-selectin expression (p < 0.05). cyanidin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 23466865-5 2013 Cyanidin, quercetin and PSPLE also significantly attenuated VCAM-1, IL-8 and CD40 expression, and quercetin significantly attenuated ICAM-1 and E-selectin expression (p < 0.05). psple 24-29 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 23388525-5 2013 The present study demonstrates that adenosine analog N-ethylcarboxyamidoadenosine (NECA) down-regulates TNF-alpha production and up-regulates IL-8 production by LPS-stimulated porcine monocytes. Adenosine 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 23388525-5 2013 The present study demonstrates that adenosine analog N-ethylcarboxyamidoadenosine (NECA) down-regulates TNF-alpha production and up-regulates IL-8 production by LPS-stimulated porcine monocytes. n-ethylcarboxyamidoadenosine 53-81 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 23388525-5 2013 The present study demonstrates that adenosine analog N-ethylcarboxyamidoadenosine (NECA) down-regulates TNF-alpha production and up-regulates IL-8 production by LPS-stimulated porcine monocytes. Adenosine-5'-(N-ethylcarboxamide) 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 23397947-3 2013 In this study we investigated whether nicotinamide (NCT), the amide form of vitamin B3, might have a protective function in reducing the expression of interleukin (IL)-1beta, IL-6, IL-8, IL-10, monocyte chemoattractant protein (MCP)-1 and tumour necrosis factor (TNF)-alpha in UV-irradiated keratinocytes. Niacinamide 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 23397947-3 2013 In this study we investigated whether nicotinamide (NCT), the amide form of vitamin B3, might have a protective function in reducing the expression of interleukin (IL)-1beta, IL-6, IL-8, IL-10, monocyte chemoattractant protein (MCP)-1 and tumour necrosis factor (TNF)-alpha in UV-irradiated keratinocytes. Amides 45-50 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 23348104-1 2013 1-nitropyrene (1-NP), a common PAH in diesel exhaust, and its amine metabolite 1-aminopyrene (1-AP) induce distinctly different chemokine-responses in bronchial epithelial cells (BEAS-2B) characterized by increases in CXCL8 and CCL5, respectively. 1-nitropyrene 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 218-223 23348104-1 2013 1-nitropyrene (1-NP), a common PAH in diesel exhaust, and its amine metabolite 1-aminopyrene (1-AP) induce distinctly different chemokine-responses in bronchial epithelial cells (BEAS-2B) characterized by increases in CXCL8 and CCL5, respectively. 1-aminopyrene 79-92 C-X-C motif chemokine ligand 8 Homo sapiens 218-223 23348104-1 2013 1-nitropyrene (1-NP), a common PAH in diesel exhaust, and its amine metabolite 1-aminopyrene (1-AP) induce distinctly different chemokine-responses in bronchial epithelial cells (BEAS-2B) characterized by increases in CXCL8 and CCL5, respectively. 1-aminopyrene 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 218-223 23422489-2 2013 In the present study, we investigated the effect of eugenol on interleukin-8 (IL-8) production by IL-1beta-stimulated oral cells. Eugenol 52-59 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 23407636-7 2013 The Ang II type 1 receptor blocker (ARB) losartan significantly blocked Ang II-induced IL-8 production. Losartan 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 23407636-8 2013 Notably, losartan blocked LPS-induced IL-8 production by THP-1 monocytes and produced a small but statistically significant reduction of baseline IL-8 production of naive THP-1 cells. Losartan 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 23407636-8 2013 Notably, losartan blocked LPS-induced IL-8 production by THP-1 monocytes and produced a small but statistically significant reduction of baseline IL-8 production of naive THP-1 cells. Losartan 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 23407636-9 2013 Losartan also produced a statistically significant increase of fluorescence intensity of naive CXCR1- and CXCR2-positive THP-1 monocytes, probably as a negative feedback effect secondary to IL-8 downregulation. Losartan 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 23407636-12 2013 Moreover, losartan suppressed the IL-8 production of naive THP-1 monocytes and LPS-treated THP-1 monocytes, suggesting a broader spectrum of pleiotropic effects. Losartan 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 23600327-5 2013 The constitutive expression of RANKL and Ki-67 and the production of IL-6 and IL-8 were significantly inhibited by Dex treatment. Dexamethasone 115-118 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 23600327-6 2013 Further, Dex significantly suppressed the stimulatory effects of LPS on RANKL and Ki-67 expression and on IL-6 and IL-8 production. Dexamethasone 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 23608554-9 2013 Additionally, significantly higher levels of IL-6 and IL-8 were observed in hydroxyurea-treated and untreated patients than in controls respectively (P = 0.04 and P = 0.01). Hydroxyurea 76-87 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 23221335-0 2013 IL-8 inhibits cAMP-stimulated alveolar epithelial fluid transport via a GRK2/PI3K-dependent mechanism. Cyclic AMP 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23422489-2 2013 In the present study, we investigated the effect of eugenol on interleukin-8 (IL-8) production by IL-1beta-stimulated oral cells. Eugenol 52-59 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 23422489-8 2013 Eugenol (5-500 muM) significantly stimulated IL-8 production in HGF cells, but had bi-modal effects on HPCs, causing slight stimulation at lower concentration (5 muM) and a significant inhibition at higher concentration (500 muM), regardless of the presence or absence of serum. Eugenol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 23391723-7 2013 The TGF-beta type I receptor kinase inhibitor LY2157299, a neutralizing TGF-beta type II receptor antibody, and SMAD4 siRNA all blocked paclitaxel-induced IL8 transcription and CSC expansion. Paclitaxel 136-146 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 23246486-3 2013 PGE2 stimulation increased SDF-1 expression in the prostate stromal cell lines WPMY-1 and NAF. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 23246486-10 2013 We also demonstrate stimulation of migration of prostate cancer cell lines PC3 and DU145 with conditioned media collected from WPMY-1 or NAF cells stimulated with PGE2 and blockade of enhanced migration by a SDF-1 neutralizing antibody. Dinoprostone 163-167 C-X-C motif chemokine ligand 8 Homo sapiens 137-140 23507231-7 2013 Phosphatidylserine inhibited the production of inflammatory mediators IL-6; IL-8; vascular endothelial growth factor; and, in particular, prostaglandin E(2) in IL-1beta-stimulated RA-FLS. Phosphatidylserines 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 23391723-7 2013 The TGF-beta type I receptor kinase inhibitor LY2157299, a neutralizing TGF-beta type II receptor antibody, and SMAD4 siRNA all blocked paclitaxel-induced IL8 transcription and CSC expansion. LY-2157299 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 23168489-5 2013 As well, we found that repeated exposures of the cells to HCHO and NO2 at concentrations that can be found indoors triggered a significant decrease in cell metabolism and an increase in IL-8 release that were not evoked by a single exposure. Nitrogen Dioxide 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 23333790-10 2013 NQ up-regulated Il-8, Tnf, and Mcp-1 genes, while AQ induced the expression of Rantes gene. nq 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 23446563-9 2013 RESULTS: Hydrogen sulfide treatment significantly increased L-selectin shedding from human neutrophils following activation by fMLP and interleukin-8 in an ADAM-17-dependent manner. Hydrogen Sulfide 9-25 C-X-C motif chemokine ligand 8 Homo sapiens 136-149 23348005-9 2013 Quercetin (10 muM) decreased TNF-alpha and IL-8 by 59.74% and 41.11% respectively and inhibited generation of lipid peroxides by 50.5%. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 23321310-0 2013 The depletion of interleukin-8 causes cell cycle arrest and increases the efficacy of docetaxel in breast cancer cells. Docetaxel 86-95 C-X-C motif chemokine ligand 8 Homo sapiens 17-30 23498787-7 2013 RESULTS: Fenoldopam preconditioning significantly decreased the serum concentrations of sCR, BUN, IL-8, and TNF-alpha in recipients. Fenoldopam 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 23439564-3 2013 PHF, DP and GA could significantly suppress the expression of allergic inflammatory cytokine IL-33-upregulated intercellular adhesion molecule (ICAM)-1, and the release of chemokines CCL2, CCL5, CXCL8 and inflammatory cytokine IL-6 from KU812 cells (all p < 0.05). phf 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 195-200 23439564-3 2013 PHF, DP and GA could significantly suppress the expression of allergic inflammatory cytokine IL-33-upregulated intercellular adhesion molecule (ICAM)-1, and the release of chemokines CCL2, CCL5, CXCL8 and inflammatory cytokine IL-6 from KU812 cells (all p < 0.05). dp 5-7 C-X-C motif chemokine ligand 8 Homo sapiens 195-200 23439564-3 2013 PHF, DP and GA could significantly suppress the expression of allergic inflammatory cytokine IL-33-upregulated intercellular adhesion molecule (ICAM)-1, and the release of chemokines CCL2, CCL5, CXCL8 and inflammatory cytokine IL-6 from KU812 cells (all p < 0.05). Gallic Acid 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 195-200 23300006-7 2013 Ethanol also induced expression of endothelial VCAM-1 and ICAM-1, production of sICAM-1 and CXCL8, and the chemokine receptors CXCR3 and CXCR4 on CD4 and CD8 lymphocytes. Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 92-97 23347248-6 2013 The greater sodium loadings in NaF and in NaI resulted from larger anion loadings in these systems. Sodium 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 22452634-7 2013 The release of CXCL8 (human homolog of murine chemokine CXCL2) by human peripheral blood mononuclear cells (PBMCs) and Jurkat cells was also reduced by FK866, as well as by sirtuin (SIRT) inhibitors and SIRT6 silencing, implying a pivotal role for this NAD(+)-dependent deacetylase in the production of this chemokine. N-(4-(1-benzoylpiperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamide 152-157 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 22452634-7 2013 The release of CXCL8 (human homolog of murine chemokine CXCL2) by human peripheral blood mononuclear cells (PBMCs) and Jurkat cells was also reduced by FK866, as well as by sirtuin (SIRT) inhibitors and SIRT6 silencing, implying a pivotal role for this NAD(+)-dependent deacetylase in the production of this chemokine. NAD 253-259 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 23333395-6 2013 IL-8 production was significantly induced in 1% O(2), with 5.5 mM glucose (p<0.01). Oxygen 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23333395-6 2013 IL-8 production was significantly induced in 1% O(2), with 5.5 mM glucose (p<0.01). Glucose 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23321310-5 2013 IL-8 depletion also increased the chemosensitivity to docetaxel. Docetaxel 54-63 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23321310-6 2013 These results indicate a role for IL-8 in promoting tumor cell survival and resistance to docetaxel and highlight the potential therapeutic significance of IL-8 depletion in ER-negative breast cancer patients. Docetaxel 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 23325889-4 2013 Use of blocking Abs and degradative enzymes demonstrated that CXCL8-stimulated filopodia formation was mediated by CXCR1 and CXCR2, Duffy Ag/receptor for chemokines, heparan sulfate (HS), and syndecans. Heparitin Sulfate 166-181 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 23275341-7 2013 We confirmed in primary cultures of normal human bronchial epithelial cells that A(2)-isoprostane inhibited ozone-induced NF-kappaB activation and IL-8 regulation. (2)-isoprostane 82-97 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 23399260-5 2013 Stimulation of IL-8 secretion by CBG40 and Zymosan was hence not due to their beta-glucan content. cbg40 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 23399260-5 2013 Stimulation of IL-8 secretion by CBG40 and Zymosan was hence not due to their beta-glucan content. Zymosan 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 23325889-4 2013 Use of blocking Abs and degradative enzymes demonstrated that CXCL8-stimulated filopodia formation was mediated by CXCR1 and CXCR2, Duffy Ag/receptor for chemokines, heparan sulfate (HS), and syndecans. Heparitin Sulfate 183-185 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 23325889-5 2013 HS was present on filopodial protrusions appearing as a meshwork on the cell surface, which colocalized with CXCL8, and this glycosaminoglycan was 2,6-O- and 3-O-sulfated. Heparitin Sulfate 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 109-114 23325889-6 2013 Transmission electron microscopy revealed that CXCL8-stimulated filopodial and microvilli-like protrusions that interacted with leukocytes before transendothelial migration and removal of HS reduced this migration. Heparitin Sulfate 188-190 C-X-C motif chemokine ligand 8 Homo sapiens 47-52 23187895-1 2013 Disodium tetrafluoroargentate(II) (Na(2)AgF(4)) has been synthesized by the thermal decomposition of NaAg(III)F(4) in the presence of NaF. disodium tetrafluoroargentate 0-29 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 24049660-11 2013 The significantly increased postchallenge concentrations of IL-2, IL-8, IL-12p70, IL-13, IL-18, IFN- gamma , TNF- alpha , and TGF- beta were released by peripheral blood cells after stimulation with PMA, as compared with both their prechallenge concentrations and with the PBS control values. Tetradecanoylphorbol Acetate 199-202 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 23187895-1 2013 Disodium tetrafluoroargentate(II) (Na(2)AgF(4)) has been synthesized by the thermal decomposition of NaAg(III)F(4) in the presence of NaF. na(2)agf 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 23149820-9 2013 Furthermore, lapatinib, which targets EGFR/HER2, inhibited the mammosphere-promoting effect of IL-8 in both HER2-positive and negative patient-derived cancers. Lapatinib 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 23408639-8 2013 The anti-leukemic effects of darinaparsin correlated with inhibition of the alternative NF-kappaB pathway and production of the inflammatory cytokine IL-8. darinaparsin 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 22924768-1 2013 BACKGROUND AND PURPOSE: Recent studies suggested a role for PGE(2) in the expression of the chemokine IL-8. Prostaglandins E 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 22924768-5 2013 KEY RESULTS: In HEK-EP(1) and HEK-EP(1) + EP(4) but not HEK or HEK-EP(4) cells, PGE(2) activated the IL-8 promoter and induced IL-8 mRNA and protein synthesis. Prostaglandins E 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 22924768-5 2013 KEY RESULTS: In HEK-EP(1) and HEK-EP(1) + EP(4) but not HEK or HEK-EP(4) cells, PGE(2) activated the IL-8 promoter and induced IL-8 mRNA and protein synthesis. Prostaglandins E 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 22924768-8 2013 In HEK-EP(1) + EP(4) cells, PGE(2) -mediated IL-8 promoter activation and IL-8 mRNA induction were blunted by inhibition of IkappaB kinase. Dinoprostone 30-36 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 22924768-12 2013 CONCLUSIONS AND IMPLICATIONS: These findings suggest that PGE(2) -mediated NF-kappaB activation by simultaneous stimulation of EP(1) and EP(4) receptors induces maximal IL-8 promoter activation and IL-8 mRNA and protein induction. Dinoprostone 58-64 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 22924768-12 2013 CONCLUSIONS AND IMPLICATIONS: These findings suggest that PGE(2) -mediated NF-kappaB activation by simultaneous stimulation of EP(1) and EP(4) receptors induces maximal IL-8 promoter activation and IL-8 mRNA and protein induction. Dinoprostone 58-64 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 22653750-5 2013 Therefore, we compared the potency of 13 different glucan preparations to induce in vitro production of IL-1beta, IL-6, IL-8 and TNF-alpha in human, whole blood cultures. Glucans 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 22749216-5 2013 Simultaneous treatment of cells with DNA and dsRNA analog poly(I:C) leads to inhibition of poly(I:C)-activated secretion of IL-6 and IL-8. Poly I-C 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 22749216-5 2013 Simultaneous treatment of cells with DNA and dsRNA analog poly(I:C) leads to inhibition of poly(I:C)-activated secretion of IL-6 and IL-8. Poly I-C 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 22788664-11 2013 Treatment with PDTC, TPCK or Bay117082 effectively antagonized LPS-induced IL-8 protein release. 3-(4-methylphenylsulfonyl)-2-propenenitrile 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 22788664-12 2013 Moreover, both the promoter activity and the LPS-induced release of IL-8 were diminished upon the administration of U0126 and SB203580, but not SP600125. U 0126 116-121 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 22788664-12 2013 Moreover, both the promoter activity and the LPS-induced release of IL-8 were diminished upon the administration of U0126 and SB203580, but not SP600125. SB 203580 126-134 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 22956122-4 2013 By reverse transcription-polymerase chain reaction and enzyme-linked immunoadsorbent assay, we demonstrated that resveratrol used in combination with polydatin was able to modulate interleukin (IL)-6, IL-8 and tumor necrosis factor-alpha gene expression. Resveratrol 113-124 C-X-C motif chemokine ligand 8 Homo sapiens 201-237 22956122-4 2013 By reverse transcription-polymerase chain reaction and enzyme-linked immunoadsorbent assay, we demonstrated that resveratrol used in combination with polydatin was able to modulate interleukin (IL)-6, IL-8 and tumor necrosis factor-alpha gene expression. polydatin 150-159 C-X-C motif chemokine ligand 8 Homo sapiens 201-237 23335378-10 2013 On the other hand, paricalcitol therapy reduced IL-8, IL-1beta, and TNF-alpha. paricalcitol 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 23335378-11 2013 CONCLUSIONS: These results further support the beneficial effects of vitamin D treatment in hemodialysis patients, since it strongly affects PAF/thrombin activities, PAF-metabolism, and IL-8, IL-1beta and TNF-alpha circulating levels. Vitamin D 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 23273744-7 2013 Hydrogen decreased the amount of IL-8 and TNF-alpha in serum, inhibited the activity of malondialdehyde and myeloperoxidase, and increased the activity of superoxide dismutase in the lung grafts from brain-dead donors. Hydrogen 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 23142559-6 2013 Furthermore, TNF-alpha-induced CXCL8 secretion was (i) inhibited by the MR antagonist tiotropium and the M3R antagonist 4-DAMP and (ii) enhanced by the M1/M3R agonist pilocarpine and the cholinesterase inhibitor physostigmine. 4-diphenylacetoxy-1,1-dimethylpiperidinium 120-126 C-X-C motif chemokine ligand 8 Homo sapiens 31-36 23142559-6 2013 Furthermore, TNF-alpha-induced CXCL8 secretion was (i) inhibited by the MR antagonist tiotropium and the M3R antagonist 4-DAMP and (ii) enhanced by the M1/M3R agonist pilocarpine and the cholinesterase inhibitor physostigmine. Pilocarpine 167-178 C-X-C motif chemokine ligand 8 Homo sapiens 31-36 23142559-6 2013 Furthermore, TNF-alpha-induced CXCL8 secretion was (i) inhibited by the MR antagonist tiotropium and the M3R antagonist 4-DAMP and (ii) enhanced by the M1/M3R agonist pilocarpine and the cholinesterase inhibitor physostigmine. Tiotropium Bromide 86-96 C-X-C motif chemokine ligand 8 Homo sapiens 31-36 23142559-6 2013 Furthermore, TNF-alpha-induced CXCL8 secretion was (i) inhibited by the MR antagonist tiotropium and the M3R antagonist 4-DAMP and (ii) enhanced by the M1/M3R agonist pilocarpine and the cholinesterase inhibitor physostigmine. Physostigmine 212-225 C-X-C motif chemokine ligand 8 Homo sapiens 31-36 23142559-7 2013 Taken as a whole, these results suggest that ACh release by A549 cells enhances TNF-alpha-induced CXCL8 secretion through activation of the M3R. Acetylcholine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 98-103 23142559-9 2013 Inhibition of these pathways with specific inhibitors abrogated the pilocarpine-induced CXCL8 release. Pilocarpine 68-79 C-X-C motif chemokine ligand 8 Homo sapiens 88-93 23142559-10 2013 Our results suggest that the TNF-alpha-induced secretion of CXCL8 in A549 cells is regulated by the release of ACh, the latter"s binding to the M3R and the downstream activation of NF-kappaB and the ERK1/2 and p38 MAPK signaling pathways. Acetylcholine 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 60-65 23425281-10 2013 Hydrocortisone in combination with low-dose infliximab potentiated the suppressive effects on TNF-alpha, IL-1beta, IL-8, and macrophage inflammatory protein-1alpha synthesis. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 23266380-0 2013 Inhibitory effects of benzodiazepines on the adenosine A(2B) receptor mediated secretion of interleukin-8 in human mast cells. Benzodiazepines 22-37 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 23433213-0 2013 [Inductive effect of zinc oxide nanoparticles on interleukin 8 gene expression in human bronchial epithelial cells and its regulatory mechanism]. Zinc Oxide 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 23433213-1 2013 OBJECTIVE: To clarify the effect of zinc oxide nanoparticles (ZnO-NPs) (30 nm in diameter) on the interleukin 8 (IL-8) gene expression in human bronchial epithelial cells (BEAS-2B) and its regulatory mechanism. Zinc Oxide 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 23433213-1 2013 OBJECTIVE: To clarify the effect of zinc oxide nanoparticles (ZnO-NPs) (30 nm in diameter) on the interleukin 8 (IL-8) gene expression in human bronchial epithelial cells (BEAS-2B) and its regulatory mechanism. Zinc Oxide 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 23433213-4 2013 RT-PCR and ELISA were used to measure the mRNA and protein expression levels of IL-8 in the BEAS-2B cells exposed to ZnO-NPs. Zinc Oxide 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 23433213-5 2013 The IL-8 mRNA decay assay was used to determine the effect of ZnO-NPs on IL-8 mRNA stability. Zinc Oxide 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 23433213-6 2013 RESULTS: Exposure to ZnO-NPs significantly increased the level of IL-8 mRNA in BEAS-2B cells and the level of IL-8 protein in supernatant medium. Zinc Oxide 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 23433213-6 2013 RESULTS: Exposure to ZnO-NPs significantly increased the level of IL-8 mRNA in BEAS-2B cells and the level of IL-8 protein in supernatant medium. Zinc Oxide 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 23433213-7 2013 The transcription inhibitor significantly reduced the mRNA expression of IL-8 induced by ZnO-NPs. Zinc Oxide 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 23433213-8 2013 ZnO-NPs significantly delayed IL-8 mRNA degradation in the BEAS-2B cells that were pretreated with actinomycin D for terminating IL-8 mRNA synthesis. Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 23433213-8 2013 ZnO-NPs significantly delayed IL-8 mRNA degradation in the BEAS-2B cells that were pretreated with actinomycin D for terminating IL-8 mRNA synthesis. Zinc Oxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 23433213-8 2013 ZnO-NPs significantly delayed IL-8 mRNA degradation in the BEAS-2B cells that were pretreated with actinomycin D for terminating IL-8 mRNA synthesis. Dactinomycin 99-112 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 23433213-8 2013 ZnO-NPs significantly delayed IL-8 mRNA degradation in the BEAS-2B cells that were pretreated with actinomycin D for terminating IL-8 mRNA synthesis. Dactinomycin 99-112 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 23266380-11 2013 In conclusion, this is the first study showing an inhibitory action of benzodiazepines on adenosine A(2B) receptor mediated interleukin-8 production in human mast (HMC1) cells. Benzodiazepines 71-86 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 23484689-2 2013 The K562 cells were treated by NHE1 specific inhibitor cariporide, the angiogenesis factors after inhibition of NHE1 were screened by using protein chip, the IL-8 expression level after cariporide treatment was detected by real-time quantitative PCR; the K562 cells with stable interference of NHE1 were constructed, the IL-8 expression level after interference of NHE1 was detected by real-time quantitative PCR; the p38 phosphorylation level in K562 cells treated with cariporide was detected by Western blot. cariporide 186-196 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 23484689-2 2013 The K562 cells were treated by NHE1 specific inhibitor cariporide, the angiogenesis factors after inhibition of NHE1 were screened by using protein chip, the IL-8 expression level after cariporide treatment was detected by real-time quantitative PCR; the K562 cells with stable interference of NHE1 were constructed, the IL-8 expression level after interference of NHE1 was detected by real-time quantitative PCR; the p38 phosphorylation level in K562 cells treated with cariporide was detected by Western blot. cariporide 186-196 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 23484689-3 2013 After treatment of K562 cells with p38 inhibitor SB203580, the IL-8 expression level was decreased by real-time quantitative PCR. SB 203580 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 23484689-4 2013 The results of protein chip showed that IL-8 expression decreased after cariporide treatment. cariporide 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 23484689-7 2013 The down-regulation of IL-8 expression induced by cariporide treatment was partially restored after K562 cells were treated with p38 inhibitor SB203580. cariporide 50-60 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 23484689-7 2013 The down-regulation of IL-8 expression induced by cariporide treatment was partially restored after K562 cells were treated with p38 inhibitor SB203580. SB 203580 143-151 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 23219793-8 2013 A 5.5- and 2-fold increase in interleukin -8 and -1beta secretion, respectively was detected 24 h following doxorubicin treatment. Doxorubicin 108-119 C-X-C motif chemokine ligand 8 Homo sapiens 30-55 23266380-3 2013 Therefore, we investigated the effects of benzodiazepines on adenosine A(2B) receptor mediated interleukin-8 production in human mast cell leukaemia (HMC1) cells by an enzyme linked immunosorbent assay. Benzodiazepines 42-57 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 23266380-4 2013 The adenosine analogue N-ethylcarboxamidoadenosine (NECA, 0.3-3 muM) increased interleukin-8 production about 5-fold above baseline. Adenosine 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 23266380-4 2013 The adenosine analogue N-ethylcarboxamidoadenosine (NECA, 0.3-3 muM) increased interleukin-8 production about 5-fold above baseline. Adenosine-5'-(N-ethylcarboxamide) 23-50 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 23266380-4 2013 The adenosine analogue N-ethylcarboxamidoadenosine (NECA, 0.3-3 muM) increased interleukin-8 production about 5-fold above baseline. Adenosine-5'-(N-ethylcarboxamide) 52-56 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 23266380-8 2013 Diazepam attenuated the NECA-induced expression of mRNA encoding for interleukin-8. Diazepam 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 69-82 23364629-17 2013 Both treatment with paricalcitol and with calcifediol produced a significant decrease in levels of IL-8 (P<.001), a known inflammatory marker, drawing attention to a trend towards better response to erythropoiesis-stimulating agents (ESAs), possibly related to the decrease in inflammation. paricalcitol 20-32 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 23339380-10 2013 HMG supplementation was able to reduce the catabolic genes" expression in cultured HACs such as matrix metalloproteinases (MMP1 & MMP3), Interleukin 1, 6 and 8 (IL-1, IL-6 & IL-8), cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS). Menotropins 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 23364629-17 2013 Both treatment with paricalcitol and with calcifediol produced a significant decrease in levels of IL-8 (P<.001), a known inflammatory marker, drawing attention to a trend towards better response to erythropoiesis-stimulating agents (ESAs), possibly related to the decrease in inflammation. Calcifediol 42-53 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 23139215-6 2013 In the immature xenograft, PCM exposure significantly attenuated LPS and IL-1beta-induced IL-8 and IL-6 expression, decreased TLR2 mRNA and TLR4 mRNA, and increased mRNA levels of specific negative regulators of inflammation, SIGIRR and Tollip. pcm 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 23129725-1 2013 Entrenched in current laboratory protocols for the measurement of plasma glucose is the false belief that sodium fluoride (NaF) is an effective inhibitor of glycolysis. Glucose 73-80 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 23610962-0 2013 Role of protein tyrosine kinase in the effect of IP6 on IL-8 secretion in intestinal epithelial cells. Phytic Acid 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 23610962-3 2013 The aim of this study was to determine the role of protein tyrosine kinase (PTK) in secretion of IL-8, a central proinflammatory cytokine, by unstimulated and IL-1beta-stimulated intestinal epithelial cells Caco-2 treated with IP6 (1 and 2.5 mM). Phytic Acid 227-230 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 23610962-5 2013 IP6 had suppressive effect on basal and IL-1beta-stimulated IL-8 secretion by cells. Phytic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 23610962-6 2013 The effect of OV on IL-8 release by cells treated with IP6 was different under constitutive and stimulated conditions. Phytic Acid 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 23610962-7 2013 Secretion of IL-8 was significantly down-regulated in cells with GEN and GEN plus IP6 treatment. Phytic Acid 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 23610962-9 2013 The results suggest that physiological intestinal concentrations of IP6 may have an inhibitory effect on IL-8 secretion by Caco-2 cells and one of the mechanisms of its action is the inhibition of PTK signaling cascade. Phytic Acid 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 22984986-5 2013 RESULTS: EC from all FRT compartments constitutively expressed NOD1, NOD2, RIG-1, and MDA5 with highest levels expressed by FT. Stimulation with poly(I:C) resulted in upregulation of NOD2, RIG-1, and MDA5 in all FRT compartments and correlated with increased secretion of IL-8, whereas estradiol treatment had no effects. Poly I-C 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 272-276 24378274-11 2013 A time- and dose-dependent upregulation of the expression of IL-6 and IL-8 mRNA was observed during the treatment at 3 and 24 h. In contrast, TNF-alpha mRNA expression was highly upregulated at 3 h after FFA exposure but returned to control values at 24 h. In conclusion, hepatocytes exposed in vitro for a short time to low FFA concentrations showed a significant upregulation of IL-6 and IL-8 to,and a rapid but transitory elevation of TNF-alpha. Fatty Acids, Nonesterified 204-207 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 24378274-11 2013 A time- and dose-dependent upregulation of the expression of IL-6 and IL-8 mRNA was observed during the treatment at 3 and 24 h. In contrast, TNF-alpha mRNA expression was highly upregulated at 3 h after FFA exposure but returned to control values at 24 h. In conclusion, hepatocytes exposed in vitro for a short time to low FFA concentrations showed a significant upregulation of IL-6 and IL-8 to,and a rapid but transitory elevation of TNF-alpha. Fatty Acids, Nonesterified 325-328 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 23127653-14 2013 Furthermore, magnolol suppressed LPS-induced IL-8 production in HEK293-mTLR4/MD-2 cells. magnolol 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 24169708-4 2013 Corrosion behaviour of Ti metal, Ti-6Al-7Nb and Ti-6Al-4V alloys and constituent metals investigated in artificial saliva is significantly affected by the presence of fluoride ions (added as NaF), as proven by electrochemical methods. Fluorides 167-175 C-X-C motif chemokine ligand 8 Homo sapiens 191-194 23121078-6 2013 RESULTS: The PDE4 inhibitor rolipram dose dependently inhibited the IL-8 secretion induced by CSE 5%. Rolipram 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 23390570-12 2013 The order of potency for inhibition of interleukin-8 release from MONOs was IL-10 >betamethasone >dexamethasone and hydrocortisone. Betamethasone 86-99 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 23390570-12 2013 The order of potency for inhibition of interleukin-8 release from MONOs was IL-10 >betamethasone >dexamethasone and hydrocortisone. Dexamethasone 104-117 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 23390570-12 2013 The order of potency for inhibition of interleukin-8 release from MONOs was IL-10 >betamethasone >dexamethasone and hydrocortisone. Hydrocortisone 122-136 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 23129725-1 2013 Entrenched in current laboratory protocols for the measurement of plasma glucose is the false belief that sodium fluoride (NaF) is an effective inhibitor of glycolysis. Sodium Fluoride 106-121 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 23129725-2 2013 The failure of NaF to properly control glycolysis decreases plasma glucose concentrations. Glucose 67-74 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 23991411-6 2013 The active form, hCaMKP-N(1-559), showed Mn(2+) or Mg(2+)-dependent phosphatase activity with a strong preference for phospho-Thr residues and was severely inhibited by NaF, but not by okadaic acid, calyculin A, or 1-amino-8-naphthol-2,4-disulfonic acid, a specific inhibitor of CaMKP. Okadaic Acid 185-197 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 22931421-8 2013 AZT down-regulated the pro-proliferative genes encoding AKT1, MYC, STAT1, MAPK8, MAPK9, CCL-3, Bcl-3, and cyclin D2; pro-angiogenenic genes encoding VEGF and IL8; and genes involved in cell adhesion (ICAM1 and FN1) and the NF-kappaB pathway. Zidovudine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 23991411-6 2013 The active form, hCaMKP-N(1-559), showed Mn(2+) or Mg(2+)-dependent phosphatase activity with a strong preference for phospho-Thr residues and was severely inhibited by NaF, but not by okadaic acid, calyculin A, or 1-amino-8-naphthol-2,4-disulfonic acid, a specific inhibitor of CaMKP. calyculin A 199-210 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 24236291-7 2013 After K562 target cell stimulation, PBMC produced profound proinflammatory and immunoregulatory cytokines/chemokines including IL-2, IL-8, IL-10, MIP-1 alpha beta , IFN- gamma , and TNF- alpha , and cytokine/chemokine secretion was related to flowcytometry-based NK cytotoxicity. PBMC 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 23991411-6 2013 The active form, hCaMKP-N(1-559), showed Mn(2+) or Mg(2+)-dependent phosphatase activity with a strong preference for phospho-Thr residues and was severely inhibited by NaF, but not by okadaic acid, calyculin A, or 1-amino-8-naphthol-2,4-disulfonic acid, a specific inhibitor of CaMKP. Chicago acid 215-253 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 23295625-0 2013 Fluoride gastrointestinal absorption from Na2FPO3/CaCO3- and NaF/SiO2-based toothpastes. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 23242618-7 2013 The stromal IL-8 positivity was associated with shorter DFS and OS in ER positive group, HER-2 negative group, and luminal A group (P < 0.05). aspartyl-phenylalanine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 23242618-7 2013 The stromal IL-8 positivity was associated with shorter DFS and OS in ER positive group, HER-2 negative group, and luminal A group (P < 0.05). Osmium 64-66 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 23710204-6 2013 Vitamin D3 acted in synergy with the TLR agonists LPS and peptidoglycan (PGN) in inducing IL-6, IL-8, and IL-10, whereas vitamin D3 completely inhibited LPS-induced secretion of IL-12. Cholecalciferol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 23571769-2 2013 Fluoride at 300 mg/l (as NaF) inhibited dissolution of native HA by 12%, while potassium and sodium dodecyl phosphates (PDP, SDP), at 0.1% or higher, inhibited dissolution by 26-34%. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 23103705-7 2013 Among patients, male gender, LVEDVi, diuretic treatment, NYHA class I, NT-proBNP and IL-8 levels were significant determinants of urine neopterin levels by bivariate analysis. Neopterin 136-145 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 23903639-5 2013 Fluoride ion release from the adhesive linearly increased with higher NaF concentration. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 70-73 23430672-11 2013 In the DEDG, significant negative correlations were detected between the Schirmer test and IL-1beta, IL6, IL8, and vascular endothelial growth factor levels, and between the fluorescein breakup time with IL6 and IL8 levels. Fluorescein 174-185 C-X-C motif chemokine ligand 8 Homo sapiens 212-215 24273918-11 2013 A positive correlation was found between serum level of IL-8 and each of GSH (r = -0.534 and p = 0.000), SOD (r = -0.295 and p = 0.021), CAT (r = -0.545 and p = 0.000), and Zn (r = 0.422 and p = 0.001) in all patient groups. Glutathione 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 24273918-11 2013 A positive correlation was found between serum level of IL-8 and each of GSH (r = -0.534 and p = 0.000), SOD (r = -0.295 and p = 0.021), CAT (r = -0.545 and p = 0.000), and Zn (r = 0.422 and p = 0.001) in all patient groups. Zinc 173-175 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 23210792-8 2013 By contrast, the stilbenes inhibited UV-connected inflammatory cytokines excluding IL-8, but they prevalently stimulated NFkappaB, EGFR nuclear translocation and the AhR-CYP pathway. Stilbenes 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 24348681-8 2013 Isolated challenge of the keratinocytes with IL-1 beta as well as with glycine resulted in an upregulation of IL6 and IL8 mRNA expression and activation of NF kappa B pathway. Glycine 71-78 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 22954322-7 2013 Whereas the poly(I:C)-induced secretion of IL-6, IP-10, and RANTES was inhibited by both IKK-2 inhibitor and LY294002, that of IL-8 was blocked only by IKK-2 inhibitor. Poly I-C 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 22954322-8 2013 CONCLUSIONS: The poly(I:C)-induced secretion of IL-6, IP-10, and RANTES from human corneal fibroblasts is mediated by both NF-kappaB and PI3K signaling pathways, whereas that of IL-8 is mediated by the NF-kappaB pathway. Poly I-C 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 22610152-3 2013 Monocyte-expressed heat shock protein 72 (HSP72) and plasma thiobarbituric acid reactive substances (TBARS) were significantly attenuated in BICARB compared to PLAC (p = 0.04 and p = 0.039, respectively), however total anti-oxidant capacity, the ratio of oxidised to total glutathione, cortisol, interleukin 6 and interleukin 8 were not significantly induced by the exercise. Sodium Bicarbonate 141-147 C-X-C motif chemokine ligand 8 Homo sapiens 314-327 24228938-5 2013 Enhanced cerussite dissolution in the presence of high salt (NaCl or NaF) concentrations leads to an increase in pyromorphite nucleation and growth rates. Salts 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 23843863-9 2013 S-[6]-Gingerol attenuated IL1beta-induced inflammation and oxidative stress in HuH7 cells, as evidenced by decreasing mRNA levels of inflammatory factor IL6, IL8, and SAA1, suppression of ROS generation, and increasing mRNA levels of DHCR24. gingerol 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 23843863-11 2013 Similar to the protective effects of S-[6]-gingerol, both NS-398 (a selective COX2 inhibitor) and PDTC (a selective NF kappa B inhibitor) suppressed mRNA levels of IL6, IL8, and SAA1. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 58-64 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 23041326-1 2013 BACKGROUND & AIMS: Interleukin (IL)-8 has an important role in initiating inflammation in humans, attracting immune cells such as neutrophils through their receptors CXCR1 and CXCR2. Adenosine Monophosphate 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 23-41 23983782-6 2013 Results showed that the hyperglycemia-induced GAG alterations in the cell surface perlecan as well as in the ECM indeed upregulated the expressions of IL-6, IL-8, and MCP-1 and the activities of MMP-2 and MMP-9 and downregulated the expressions of TIMP-2. Glycosaminoglycans 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 23795507-10 2013 However, the degree of ionic absorption within the brush is again ion specific n the order NaCl > NaBr > NaI > NaF at 1 m salt concentration. Sodium Chloride 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 23795507-10 2013 However, the degree of ionic absorption within the brush is again ion specific n the order NaCl > NaBr > NaI > NaF at 1 m salt concentration. sodium bromide 101-105 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 23795507-10 2013 However, the degree of ionic absorption within the brush is again ion specific n the order NaCl > NaBr > NaI > NaF at 1 m salt concentration. Sodium Iodide 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 23795507-10 2013 However, the degree of ionic absorption within the brush is again ion specific n the order NaCl > NaBr > NaI > NaF at 1 m salt concentration. Salts 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 23795509-5 2013 Its maximum, however, is shifted towards higher DOTAP concentrations in the row: NaF < NaCl < NaBr. 1,2-dioleoyloxy-3-(trimethylammonium)propane 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 23935691-0 2013 Modulation of the expression of the proinflammatory IL-8 gene in cystic fibrosis cells by extracts deriving from olive mill waste water. Water 130-135 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 23935691-2 2013 Polyphenols rich extracts derived from waste water from olive mill, obtained by a molecular imprinting approach, have been investigated in order to discover compounds able to reduce IL-8 expression in human bronchial epithelial cells (IB3-1 cells), derived from a CF patient with a DeltaF508/W1282X mutant genotype and stimulated with TNF-alpha. Polyphenols 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 23935691-5 2013 Utilizing TNF-alpha-treated IB3-1 cells as experimental model system, we demonstrated that apigenin and cyanidin chloride are able to modulate the expression of the NF-kappaB-regulated IL-8 gene, while oleuropein showed no effect in regulating the expression of the gene IL-8. Apigenin 91-99 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 23935691-5 2013 Utilizing TNF-alpha-treated IB3-1 cells as experimental model system, we demonstrated that apigenin and cyanidin chloride are able to modulate the expression of the NF-kappaB-regulated IL-8 gene, while oleuropein showed no effect in regulating the expression of the gene IL-8. Apigenin 91-99 C-X-C motif chemokine ligand 8 Homo sapiens 271-275 23935691-5 2013 Utilizing TNF-alpha-treated IB3-1 cells as experimental model system, we demonstrated that apigenin and cyanidin chloride are able to modulate the expression of the NF-kappaB-regulated IL-8 gene, while oleuropein showed no effect in regulating the expression of the gene IL-8. cyanidin 104-121 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 23935691-5 2013 Utilizing TNF-alpha-treated IB3-1 cells as experimental model system, we demonstrated that apigenin and cyanidin chloride are able to modulate the expression of the NF-kappaB-regulated IL-8 gene, while oleuropein showed no effect in regulating the expression of the gene IL-8. cyanidin 104-121 C-X-C motif chemokine ligand 8 Homo sapiens 271-275 23795509-5 2013 Its maximum, however, is shifted towards higher DOTAP concentrations in the row: NaF < NaCl < NaBr. Sodium Chloride 90-94 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 23795509-5 2013 Its maximum, however, is shifted towards higher DOTAP concentrations in the row: NaF < NaCl < NaBr. sodium bromide 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 23041326-8 2013 IL-8 was strongly up-regulated on systemic or local inflammatory stimulation, increasing mobilization of immature CD11b(+)Gr-1(+) myeloid cells (IMCs) with thioglycolate-induced peritonitis, DSS-induced colitis, and H. felis-induced gastritis. Thioglycolates 156-169 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23041326-8 2013 IL-8 was strongly up-regulated on systemic or local inflammatory stimulation, increasing mobilization of immature CD11b(+)Gr-1(+) myeloid cells (IMCs) with thioglycolate-induced peritonitis, DSS-induced colitis, and H. felis-induced gastritis. dss 191-194 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23711848-0 2013 Effect of formoterol on eosinophil trans-basement membrane migration induced by interleukin-8-stimulated neutrophils. Formoterol Fumarate 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 80-93 23711848-3 2013 In this study, we investigated whether formoterol modified the trans-basement membrane migration (TBM) of eosinophils stimulated with neutrophils and IL-8. Formoterol Fumarate 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 23711858-3 2013 Here, we examined the effects of the glucocorticoid fluticasone propionate (FP) on the expression of the inflammatory chemokines CCL5, CXCL8 and CXCL10. Fluticasone 52-74 C-X-C motif chemokine ligand 8 Homo sapiens 135-140 23711848-10 2013 RESULTS: A combination of neutrophils and IL-8 significantly induced the eosinophil TBM; formoterol alone had no effect. eosinophil tbm 73-87 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 23159604-0 2013 A vitamin D3 analog augmented interleukin-8 production by human monocytic cells in response to various microbe-related synthetic ligands, especially NOD2 agonistic muramyldipeptide. Cholecalciferol 2-12 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 23711848-11 2013 However, formoterol modestly but significantly attenuated the TBM of eosinophils stimulated with neutrophils and IL-8. Formoterol Fumarate 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 24024768-9 2013 Only TRP significantly decreased serum levels of apolipoprotein B (apoB; -6%), interleukin-8 (IL-8; -11%) and monocyte chemotactic protein-1 (MCP-1; -19%). Tryptophan 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 23781245-7 2013 The mean Knoop hardness number (KHN) of 5% NaF with fTCP was greater than that of 5% NaF alone while the control group had the lowest mean KHN. 4-Fluoro-1-(1-(2-thienyl)cyclohexyl)piperidine 52-56 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 24024768-9 2013 Only TRP significantly decreased serum levels of apolipoprotein B (apoB; -6%), interleukin-8 (IL-8; -11%) and monocyte chemotactic protein-1 (MCP-1; -19%). Tryptophan 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 22841520-5 2013 RESULTS: Compared to placebo, metformin reduced monocyte release of tumor necrosis factor-alpha, interleukin-1beta, interleukin-6, monocyte chemoattractant protein-1 and interleukin-8, as well as decreased plasma C-reactive protein levels, which were accompanied by an improvement in insulin sensitivity. Metformin 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 170-183 23197259-8 2013 YKL-40-induced IL-8 was found to further stimulate proliferation and migration of BSMCs, and the effects were inhibited after neutralizing IL-8. bsmcs 82-87 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 23197259-8 2013 YKL-40-induced IL-8 was found to further stimulate proliferation and migration of BSMCs, and the effects were inhibited after neutralizing IL-8. bsmcs 82-87 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 23197259-9 2013 Through investigating the interaction of airway epithelium and smooth muscle, our findings implicate that YKL-40 may be involved in the inflammation of asthma by induction of IL-8 from epithelium, subsequently contributing to BSMC proliferation and migration. bsmc 226-230 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 23228258-9 2013 Levels of proinflammatory cytokines (eg, interleukin 6, interleukin 8, and matrix metalloproteinase-3 [MMP3]) were increased by CQ treatment. camphorquinone 128-130 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 23365588-3 2013 For the first method, blood samples were collected in tubes containing sodium fluoride (NaF), a glycolysis inhibitor. Sodium Fluoride 71-86 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 23566357-12 2013 CONCLUSIONS: Changes in the pre- and post-treatment profiles of BDNF in CSF and blood, HGF in CSF and CXCL8 (IL-8) in serum, suggest that minocycline may have effects in the CNS by modulating the production of neurotrophic growth factors. Minocycline 138-149 C-X-C motif chemokine ligand 8 Homo sapiens 102-107 23566357-12 2013 CONCLUSIONS: Changes in the pre- and post-treatment profiles of BDNF in CSF and blood, HGF in CSF and CXCL8 (IL-8) in serum, suggest that minocycline may have effects in the CNS by modulating the production of neurotrophic growth factors. Minocycline 138-149 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 23533307-8 2013 rSAA also affected the production of compounds present in the tumor microenvironment that orchestrate tumor progression, such as IL-8, the production of reactive oxygen species (ROS) and nitric oxide (NO). rsaa 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 22971992-11 2013 EGCG modulated markers of cell cycle (p27/KIP1), angiogenesis (CD31, VEGF, IL-6, IL-8, SEMA3F, and HIF1alpha), and metastasis (MMP2 and MMP7). epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 23878839-15 2013 Enamel F uptake by NaF and NaF/MFP was significantly greater than MFP dentifrices (P < 0.05 to P < 0.001), with the area under the depth curve being 2.4 and 2.2 times greater, respectively. enamel f 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 23182920-9 2013 Bilirubin increased basal production of IL-8 and IL-1beta, but downregulated LPS-induced generation of IL-8 and MIP-1beta. Bilirubin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 23182920-9 2013 Bilirubin increased basal production of IL-8 and IL-1beta, but downregulated LPS-induced generation of IL-8 and MIP-1beta. Bilirubin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 23924923-9 2013 HGF-induced expression of Ets-1 and IL-8 was increased more by GRP treatment and inhibited by pretreatment with an ERK 1/2 inhibitor (PD098059). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 24030317-5 2013 RESULTS: Histamine upregulated IL-6 and IL-8 expression and IL-6 and IL-8 secretion in a dose-dependent manner in HCEC. Histamine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 24030317-5 2013 RESULTS: Histamine upregulated IL-6 and IL-8 expression and IL-6 and IL-8 secretion in a dose-dependent manner in HCEC. Histamine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 24030317-6 2013 Niflumic acid (NFA), an hCLCA blocker, reduced histamine-induced IL-6 and IL-8 expression. Niflumic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24030317-6 2013 Niflumic acid (NFA), an hCLCA blocker, reduced histamine-induced IL-6 and IL-8 expression. Niflumic Acid 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24030317-6 2013 Niflumic acid (NFA), an hCLCA blocker, reduced histamine-induced IL-6 and IL-8 expression. Histamine 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 24030317-7 2013 CONCLUSION: Histamine-induced IL-6 and IL-8 production could be attenuated by NFA, an hCLCA blocker. Histamine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 24018975-4 2013 We demonstrate that miR-200 inhibits angiogenesis through direct and indirect mechanisms by targeting interleukin-8 and CXCL1 secreted by the tumour endothelial and cancer cells. mir-200 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 23887394-12 2013 15d-PGJ2 downregulated LPS-induced IL-8 and MCP-1 production. 15-deoxyprostaglandin J2 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 23878839-14 2013 Overall, the degree of remineralisation was as follows: NaF-silica-pyrophosphate dentifrices (1000 ppm F) averaged 41%; NaF/MFP-silica (1500/1000 ppm F) 38%; MFP/NaF-dicalcium phosphate (1000/450 ppm F) 30%; MFP dentifrices (1000 ppm F) ranged from 15 to 23%. silica-pyrophosphate 60-80 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 23878839-14 2013 Overall, the degree of remineralisation was as follows: NaF-silica-pyrophosphate dentifrices (1000 ppm F) averaged 41%; NaF/MFP-silica (1500/1000 ppm F) 38%; MFP/NaF-dicalcium phosphate (1000/450 ppm F) 30%; MFP dentifrices (1000 ppm F) ranged from 15 to 23%. Silicon Dioxide 60-66 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 24030317-7 2013 CONCLUSION: Histamine-induced IL-6 and IL-8 production could be attenuated by NFA, an hCLCA blocker. Niflumic Acid 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 23878839-15 2013 Enamel F uptake by NaF and NaF/MFP was significantly greater than MFP dentifrices (P < 0.05 to P < 0.001), with the area under the depth curve being 2.4 and 2.2 times greater, respectively. enamel f 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 24030317-1 2013 BACKGROUND/AIMS: Histamine remains the main mediator of allergic conjunctivitis and induces interleukin (IL)-6 and IL-8 production in human conjunctival epithelial cells (HCEC). Histamine 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 24030317-2 2013 The purpose of the present study was to determine whether histamine induced IL-6 and IL-8 expression in HCEC, and to describe the relationship between human calcium-activated chloride channel (hCLCA) 1 activity and IL-6 and IL-8 expression. Histamine 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 23573194-8 2013 Budesonide with Formoterol reduced IL-17A and RORgamma(t), while increased FOXP3 in cultured T-lymphocytes from mild-moderate asthma/persistent rhinitis, and reduced the IL-8 release mediated by IL-17A present in NW and Ss from mild-moderate asthma/persistent rhinitis in nasal and bronchial epithelial cells. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 23844276-6 2013 Arachidonic acid and saturated fatty acids (SFAs) both demonstrate an ability to increase pro-inflammatory IL-8 along with numerous other inflammatory factors including IL-6, TNF alpha , IL-1 beta , and CXCL1 for arachidonic acid and IGB2 and CTSS for SFA. Arachidonic Acid 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23844276-6 2013 Arachidonic acid and saturated fatty acids (SFAs) both demonstrate an ability to increase pro-inflammatory IL-8 along with numerous other inflammatory factors including IL-6, TNF alpha , IL-1 beta , and CXCL1 for arachidonic acid and IGB2 and CTSS for SFA. Fatty Acids 21-42 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23840918-7 2013 Luteolin and kaempferol significantly reduced LPS-induced secretion of proinflammatory cytokines (IL-6 and IL-8) and prostaglandins (PGE(2) and PGF(2alpha)) in fetal membranes, IL-1beta-induced COX-2 gene expression and prostaglandin production in myometrium, and IL-1beta-induced MMP-9 activity in amnion and myometrial cells. kaempferol 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 23555637-4 2013 METHODS AND RESULTS: Confluent human umbilical vein endothelial cell (HUVECs ) treated with atorvastatin demonstrated significantly decreased lipopolysaccharide (LPS)-mediated IL-6 and IL-8 generation. Atorvastatin 92-104 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 23573194-8 2013 Budesonide with Formoterol reduced IL-17A and RORgamma(t), while increased FOXP3 in cultured T-lymphocytes from mild-moderate asthma/persistent rhinitis, and reduced the IL-8 release mediated by IL-17A present in NW and Ss from mild-moderate asthma/persistent rhinitis in nasal and bronchial epithelial cells. Formoterol Fumarate 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 23383243-8 2013 Incubation of PMNs with the tripeptide N-ac-PGP resulted in the release of CXCL8, MMP8 and MMP9. tripeptide K-26 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 75-80 23527233-0 2013 Resveratrol induces long-lasting IL-8 expression and peculiar EGFR activation/distribution in human keratinocytes: mechanisms and implications for skin administration. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 23527233-7 2013 Resveratrol induced delayed, long-lasting and steadily growing IL-8 gene and protein over-expression as well as enhanced EGFR phosphorylation, both abrogated by the EGFR kinase inhibitor PD168393. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 23527233-7 2013 Resveratrol induced delayed, long-lasting and steadily growing IL-8 gene and protein over-expression as well as enhanced EGFR phosphorylation, both abrogated by the EGFR kinase inhibitor PD168393. PD168393 187-195 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 23527233-12 2013 CONCLUSIONS/SIGNIFICANCE: Resveratrol synergized with TNFalpha in the induction of delayed, long-lasting IL-8 expression through sustained EGFR-ERK axis activation. Resveratrol 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 23326479-8 2013 RESULTS: DON induced a pro-inflammatory response with a significant increase of expression of mRNA encoding for IL-8, IL-1alpha and IL-1beta, TNF-alpha in all used models. deoxynivalenol 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 23308155-6 2013 RESULTS: The effusion size and effusion VEGF, IL-8 and PAI-1/tPA ratio were significantly higher in CPPE than in UPPE, and significantly higher in multi-loculated PPE than in non-locualted and uni-loculated PPE, respectively. ppe 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 24459828-10 2013 Stimulation with PolyI:C, Pam3CSK4 and LPS also lead to considerable increase of NF-kBp65, while increased levels of inflammatory cytokines were observed for IL-8, TNF and IL-6 in cells treated with PMA and MeV. Poly I-C 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 24204381-8 2013 These results suggest that 15d-PGJ2 suppresses activin-induced ActR and Smad expression, down-regulates IL-6 production, and up-regulates IL-8 production via suppression of NF- kappa B and MAPK signaling pathway in HepG2 cells. 15-deoxy-delta(12,14)-prostaglandin J2 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 23117134-6 2013 Caffeine decreased (P < 0.05) both the number of total uterine PMNs and expression of IL-8 mRNA in the endometrium after AI. Caffeine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 23117134-9 2013 In conclusion, the addition of caffeine to the thawing solution inhibited migration of uterine PMNs, probably by downregulating IL-8 mRNA expression in the endometrium. Caffeine 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 23294717-10 2013 At 48 h after 10(-7); or 10(-6); mol/L DEX was added, IL-8 levels in the culture supernatants of the hypoxia groups were higher than those in the corresponding normoxia groups (P<0.05). Dexamethasone 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 22985912-5 2013 The secretion of proinflammatory products was strongly stimulated by sequential incubation of EC with iodixanol and TNFalpha (p<0.00001 for all tested molecules, namely TNFalpha, IL-8, sVCAM-1, MCP-1, and IL-6). iodixanol 102-111 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 22975265-11 2012 C3 and IL-8 transcript levels were increased in pemetrexed-treated Lo cells relative to Lo controls; DHFR transcript levels were decreased. Pemetrexed 48-58 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 23256107-5 2012 IL-8 serum levels were higher in the first (P&lt;0.0001) and third (P=0.003) trimesters of pregnancy in SLE patients compared with controls, INF-gamma serum levels in the third trimester (P=0.009), and IL-10 serum levels in the first and third trimesters (P=0.055 and P&lt;0.0001, respectively). Adenosine Monophosphate 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23259744-10 2012 In M10 cells, TMZ promoted NF-kappaB2/p52 generation and nuclear translocation and enhanced the secretion of IL-8 and MCP-1. Temozolomide 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 23070150-9 2012 The IL-8 cytokine response was found to be significantly lower for the magnetite nanoparticles compared to TiO(2), while an enhancement of ROS was observed, which was further increased for the ATP-modified nanoparticles, implicating involvement of the ATP signalling pathway in the epithelium. Adenosine Triphosphate 193-196 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 22975265-12 2012 In Lo cells, IL-8 and C3 protein concentrations were increased following pemetrexed treatment. Pemetrexed 73-83 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 23263807-0 2012 Inhibitory effect on TNF-alpha-induced IL-8 secretion in HT-29 cell line by glyceroglycolipids from the leaves of Ficus microcarpa. glyceroglycolipids 76-94 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 22944462-8 2012 Pretreatment with LDFL at 20, 10 or 1 ng/ml reduced HDFL-induced IL-8 production by 61%, 52% and 40%, respectively (p<0.05). ldfl 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 22551309-4 2012 We report here our conclusions based on data from past studies that seizures are associated with elevated interleukin-8 (IL-8) and that dapsone inhibits IL-8 release and function in several different clinical and experimental contexts. Dapsone 136-143 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 23089469-4 2012 This study was to investigate the influence of therapeutic concentrations of prazosin (0.01 and 0.1muM) on cell proliferation and differential expressions of CCL2, CCL20, CXCL6, CXCL10, IL8 and IL6 genes related to inflammation and/or oxidative stress in human HCC cell lines. Prazosin 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 186-189 23399841-4 2012 Suppressing ROCK with the Y27632 inhibitor suppressed IL-1-stimulated Caco-2 cell CXCL8/IL-8 and IEC-6 cell CCL2/MCP-1 secretion and mRNA levels. Y 27632 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 82-87 23399841-4 2012 Suppressing ROCK with the Y27632 inhibitor suppressed IL-1-stimulated Caco-2 cell CXCL8/IL-8 and IEC-6 cell CCL2/MCP-1 secretion and mRNA levels. Y 27632 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 23154477-1 2012 A 46-year-old female patient with infiltrating ductal carcinoma had an F-fluoride PET which demonstrated uptake in multiple skeletal metastasis and several upper abdominal lesions corresponding to liver metastases on contrast enhanced CT. F-NaF uptake in soft tissue metastases are likely to be more frequently encountered with the increasing use of F-NaF PET/CT in oncology. f-fluoride 71-81 C-X-C motif chemokine ligand 8 Homo sapiens 241-244 23154477-1 2012 A 46-year-old female patient with infiltrating ductal carcinoma had an F-fluoride PET which demonstrated uptake in multiple skeletal metastasis and several upper abdominal lesions corresponding to liver metastases on contrast enhanced CT. F-NaF uptake in soft tissue metastases are likely to be more frequently encountered with the increasing use of F-NaF PET/CT in oncology. f-fluoride 71-81 C-X-C motif chemokine ligand 8 Homo sapiens 352-355 22885734-7 2012 RESULTS: The mRNA expressions of CCL3, CCL4, and CXCL8 were up-regulated by IL-1beta and down-regulated by tacrolimus. Tacrolimus 107-117 C-X-C motif chemokine ligand 8 Homo sapiens 49-54 23397001-6 2012 However, all three different sizes of silica nanoparticles induced IL-8 production. Silicon Dioxide 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 23397001-9 2012 Therefore, IL-8 production induced by silica nanoparticles may be dependent on other mechanisms rather than intracellular Ca(++) increase and ROS generation. Silicon Dioxide 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 22990619-5 2012 Plasma TNF-alpha and IL-8 levels were significantly higher in long-term heroin-dependent patients than in healthy controls (p < 0.001). Heroin 72-78 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 22763784-7 2012 To investigate the anti-inflammatory potential of EGCG, we evaluated pro-inflammatory cytokine synthesis in IGF-I-differentiated SZ95 sebocytes and found that expression of IL-1, IL-6, and IL-8 was decreased. epigallocatechin gallate 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 22990619-6 2012 Chronic heroin-use-induced TNF-alpha and IL-8 levels were significantly (p < 0.05) attenuated in patients treated for 12 weeks with add-on dextromethorphan. Heroin 8-14 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 22990619-6 2012 Chronic heroin-use-induced TNF-alpha and IL-8 levels were significantly (p < 0.05) attenuated in patients treated for 12 weeks with add-on dextromethorphan. Dextromethorphan 142-158 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 23046766-5 2012 The estimated 40% inhibitory concentration (IC(40)) of TEI-A00114 on interleukin (IL)-8 production induced by lipopolysaccharide and on IL-1beta in human whole blood cells in vitro were 9.8 x 10(-8) or 1.8 x 10(-9)M, respectively. (2-hydroxy-2-methyl-cyclopentanone-5-ylidene)methyl-9,10-secopregna-5,7,10(19)-triene-1,3-diol 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 69-87 23088987-1 2012 PURPOSE: We characterized and identified the uroepithelial P2 receptor responsible for adenosine triphosphate mediated release of the cytokines interleukin-8 and 6. Adenosine Triphosphate 87-109 C-X-C motif chemokine ligand 8 Homo sapiens 144-163 23088987-9 2012 Signaling pathway experiments showed that interleukin-8 release involved phospholipase C and inositol trisphosphate mediated signaling, indicating a P2Y receptor subtype. inositol 1,2,3-trisphosphate 93-115 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 23088987-11 2012 Gene expression analysis of P2 receptors showed that strong expression of P2Y(2) receptor and subsequent knockdown of P2Y(2) receptor mRNA for 72 and 96 hours abrogated interleukin-8 and 6 release after purinergic stimulation with adenosine triphosphate-gamma-S. adenosine triphosphate-gamma-s 231-261 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 23086146-8 2012 Our previous nuclear magnetic resonance studies indicate that IL-8 binding to the N-terminal residues is mediated by the membrane, underscoring the importance of the phospholipid bilayer for physiological activity. phospholipid bilayer 166-186 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 23132229-8 2012 Exogenous H(2)S inhibited the TNF-alpha-mediated upregulation of NO, IL-6 and IL-8 in a dose-dependent manner. Hydrogen Sulfide 10-15 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 23327913-20 2012 The contents of IL-8 in supernatants of normal fibroblasts in 1.00-4.00 mmol/L oleic acid groups were markedly higher than those in BC and EC groups (F = 2.717, P < 0.05 or P < 0.01). Oleic Acid 79-89 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 23327913-21 2012 The contents of IL-8 in supernatants of scar fibroblasts in 2.00 and 4.00 mmol/L oleic acid groups were significantly higher than those in BC and EC groups (F = 3.338, P < 0.05). Oleic Acid 81-91 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 23086953-7 2012 SIRT6 increases the nuclear levels of the Ca(2+)-dependent transcription factor, nuclear factor of activated T cells (NFAT), and cyclosporin A, a calcineurin inhibitor that reduces NFAT activity, reduces TNF and IL8 expression in SIRT6-overexpressing cells. Cyclosporine 129-142 C-X-C motif chemokine ligand 8 Homo sapiens 212-215 22935637-6 2012 Either the selective bradykinin B(2) receptor antagonist HOE 140 or the selective bradykinin B(1) receptor antagonist Lys-(des-Arg(9), Leu(8))-bradykinin alone halved IL-8 release and the combination of both drugs suppressed this effect. lys-(des-arg 118-130 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 23181472-8 2012 A differential secretion of CXCL8 and CCL2 was observed upon oligosaccharide co-cultivation with colorectal epithelial Caco-2 cells. Oligosaccharides 61-76 C-X-C motif chemokine ligand 8 Homo sapiens 28-33 22983351-0 2012 Cigarette smoke and its component acrolein augment IL-8/CXCL8 mRNA stability via p38 MAPK/MK2 signaling in human pulmonary cells. Acrolein 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 22983351-0 2012 Cigarette smoke and its component acrolein augment IL-8/CXCL8 mRNA stability via p38 MAPK/MK2 signaling in human pulmonary cells. Acrolein 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 56-61 22983351-6 2012 Furthermore, pharmacological inhibition of p38 MAPK or MK2 strongly accelerated the decay of IL-8 mRNA levels upon stimulation with CSE or acrolein and subsequent blockade of mRNA neosynthesis with actinomycin D in pulmonary structural cells (HBSMCs and airways epithelial cells) as well as in human alveolar macrophages. Acrolein 139-147 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 23041168-11 2012 In conclusions, it is suggested that IL-1beta, IL-6, IL-8 and TNF-alpha were associated with TCE-induced hypersensitivity dermatitis. Trichloroethylene 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 23285690-10 2012 The findings of this study show that p38 MAPK could be one of the molecular targets for IP6 in the intestinal epithelial cells and that IP6 inhibitory effect on IL-8 secretion by Caco-2 cells could be mediated by its inhibition of p38 activity. Phytic Acid 136-139 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. Amines 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 199-212 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. Amines 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. Amines 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 23285696-0 2012 The effect of phytic acid on the expression of NF-kappaB, IL-6 and IL-8 in IL-1beta-stimulated human colonic epithelial cells. Phytic Acid 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. poly(lactide) 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 199-212 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. poly(lactide) 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. poly(lactide) 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. cplas 66-71 C-X-C motif chemokine ligand 8 Homo sapiens 199-212 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. cplas 66-71 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. cplas 66-71 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 23285690-0 2012 Phytic acid down-regulates IL-8 secretion from colonic epithelial cells by influencing mitogen-activated protein kinase signaling pathway. Phytic Acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 23285690-6 2012 Furthermore, the role of signaling pathways involving p38 MAP kinase in IP6-induced down-regulation of IL-8 secretion by unstimulated and IL-1beta-stimulated cells in the presence of p38 MAP kinase activator (anisomycin) and inhibitor (SB 203580) was evaluated. Phytic Acid 72-75 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 23285690-9 2012 The similar level of p38alpha mRNA was found in untreated and treated with IP6 cells after 6 and 12 h. Incubation of Caco-2 cells with anisomycin resulted in upregulation of IL-8 secretion and their pretreatment with anisomycin prior to IP6 addition showed down-regulation of IL-8 secretion compared to cells treated with anisomycin alone. Phytic Acid 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 23285690-9 2012 The similar level of p38alpha mRNA was found in untreated and treated with IP6 cells after 6 and 12 h. Incubation of Caco-2 cells with anisomycin resulted in upregulation of IL-8 secretion and their pretreatment with anisomycin prior to IP6 addition showed down-regulation of IL-8 secretion compared to cells treated with anisomycin alone. Anisomycin 135-145 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 23285690-9 2012 The similar level of p38alpha mRNA was found in untreated and treated with IP6 cells after 6 and 12 h. Incubation of Caco-2 cells with anisomycin resulted in upregulation of IL-8 secretion and their pretreatment with anisomycin prior to IP6 addition showed down-regulation of IL-8 secretion compared to cells treated with anisomycin alone. Anisomycin 135-145 C-X-C motif chemokine ligand 8 Homo sapiens 276-280 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. poly(lactide) 52-63 C-X-C motif chemokine ligand 8 Homo sapiens 199-212 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. poly(lactide) 52-63 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 23285696-7 2012 The aim of this study was to analyze the effect of IP6 on the expression of IL-6 and IL-8 as well as p50 and p65 subunits of NF-kappaB and its inhibitor IkappaBalpha in Caco-2 cells stimulated with IL-1beta. Phytic Acid 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 23184827-1 2012 Well-defined tertiary amine-functionalized cationic polylactides (CPLAs) are synthesized by thiol-ene click functionalization of an allyl-functionalized polylactide, and utilized for the delivery of interleukin-8 (IL-8) siRNA via CPLA-IL-8 siRNA nanoplexes. poly(lactide) 52-63 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 23184827-4 2012 It is found that the degradability and cytotoxicity of CPLAs, as well as the transfection efficiency of the CPLA-IL-8 siRNA nanoplexes, positively correlate with the amine mol% of CPLAs. Amines 166-171 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 23285696-10 2012 Treatment of cells with IP6 resulted in a marked decrease in both IL-6 (at 3 and 6 h) and IL-8 expression (3 h). Phytic Acid 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 23184827-4 2012 It is found that the degradability and cytotoxicity of CPLAs, as well as the transfection efficiency of the CPLA-IL-8 siRNA nanoplexes, positively correlate with the amine mol% of CPLAs. cplas 180-185 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 23285696-11 2012 The results of these studies suggest that IP6 may exert immunoregulatory effects on intestinal epithelium by influencing transcriptional activity of genes encoding p50 subunit of NF-kappaB, its inhibitor IkappaBalpha and proinflammatory cytokines IL-6 and IL-8. Phytic Acid 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 22580394-0 2012 Increase of toll-like receptor 4 but decrease of interleukin-8 mRNA expression among ischemic stroke patients under aspirin treatment. Aspirin 116-123 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 23038702-10 2012 There were significant correlations between CGRP and IL-6 changes (P = 0.011) and between DLQI and IL-8 changes (P = 0.026) in the curcumin group. Curcumin 131-139 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 23038702-11 2012 In the curcumin group, changes in serum IL-8 concentrations were found as the significant predictor of DLQI scores (P = 0.026) but none of the independent variables could predict pruritus scores. Curcumin 7-15 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 22729138-11 2012 CONCLUSION: The phIGFBP-1 test is a fast and easy test that can be used with Bishop score and IL-8 to reach an high positive predictive value in the prediction of the success of labour induction with prostaglandins. Prostaglandins 200-214 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 22580394-8 2012 A reduction of IL-8 expression could result from the downregulatory effects of aspirin. Aspirin 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 23051921-0 2012 PGE2 induces interleukin-8 derepression in human astrocytoma through coordinated DNA demethylation and histone hyperacetylation. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 23051921-1 2012 We have recently reported that in astrocytoma cells the expression of interleukin-8 (IL-8) is upregulated by prostaglandin E2 (PGE2). Dinoprostone 109-125 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 23051921-1 2012 We have recently reported that in astrocytoma cells the expression of interleukin-8 (IL-8) is upregulated by prostaglandin E2 (PGE2). Dinoprostone 109-125 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 23051921-1 2012 We have recently reported that in astrocytoma cells the expression of interleukin-8 (IL-8) is upregulated by prostaglandin E2 (PGE2). Dinoprostone 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 23051921-1 2012 We have recently reported that in astrocytoma cells the expression of interleukin-8 (IL-8) is upregulated by prostaglandin E2 (PGE2). Dinoprostone 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 23051921-3 2012 Here, we have investigated whether IL-8 activation by PGE2 involves changes in DNA methylation and/or histone modifications in 46 astrocytoma specimens, two astrocytoma cell lines and normal astrocytic cells. Dinoprostone 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 23051921-4 2012 The DNA methylation status of the IL-8 promoter was analyzed by bisulphite sequencing and by methylation DNA immunoprecipitation analysis. hydrogen sulfite 64-74 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 23051921-6 2012 IL-8 expression at promoter, mRNA and protein level was explored by transfection, real-time PCR and enzyme immunoassay experiments in cells untreated or treated with PGE2, 5-aza-2"-deoxycytidine (5-aza-dC) and HDAC inhibitors, alone or in combination. Dinoprostone 166-170 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23051921-6 2012 IL-8 expression at promoter, mRNA and protein level was explored by transfection, real-time PCR and enzyme immunoassay experiments in cells untreated or treated with PGE2, 5-aza-2"-deoxycytidine (5-aza-dC) and HDAC inhibitors, alone or in combination. Decitabine 172-194 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23051921-6 2012 IL-8 expression at promoter, mRNA and protein level was explored by transfection, real-time PCR and enzyme immunoassay experiments in cells untreated or treated with PGE2, 5-aza-2"-deoxycytidine (5-aza-dC) and HDAC inhibitors, alone or in combination. Decitabine 196-204 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 23051921-8 2012 We observed that PGE2 induced IL-8 activation through: (1) demethylation of the single CpG site 5 located at position -83 within the binding region for CEBP-beta in the IL-8 promoter; (2) C/EBP-beta and p300 co-activator recruitment; (3) H3 acetylation enhancement and (4) reduction in DNMT1, DNMT3a, HDAC2 and HDAC3 association to CpG site 5 region. Dinoprostone 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 23051921-8 2012 We observed that PGE2 induced IL-8 activation through: (1) demethylation of the single CpG site 5 located at position -83 within the binding region for CEBP-beta in the IL-8 promoter; (2) C/EBP-beta and p300 co-activator recruitment; (3) H3 acetylation enhancement and (4) reduction in DNMT1, DNMT3a, HDAC2 and HDAC3 association to CpG site 5 region. Dinoprostone 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 23051921-9 2012 Treatment with 5-aza-dC or HDAC inhibitors of class I HDACs strengthened either basal or PGE2-mediated IL-8 expression. Azacitidine 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 23051921-9 2012 Treatment with 5-aza-dC or HDAC inhibitors of class I HDACs strengthened either basal or PGE2-mediated IL-8 expression. Dinoprostone 89-93 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 23051921-10 2012 These findings have elucidated an orchestrated mechanism triggered by PGE2 whereby concurrent association of site-specific demethylation and histone H3 hyperacetylation resulted in derepression of IL-8 gene expression in human astrocytoma. Dinoprostone 70-74 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 22899568-6 2012 Both TG accumulation and IL-8 secretion were shown to be dependent on ceramide production by specific knock-down of NSM2. Ceramides 70-78 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 22696056-0 2012 Vitiligo-inducing phenols activate the unfolded protein response in melanocytes resulting in upregulation of IL6 and IL8. Phenols 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 22696056-9 2012 Co-treatment with XBP1 inhibitors reduced IL6 and IL8 production induced by phenols, while overexpression of XBP1 alone increased their expression. Phenols 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 22946548-5 2012 In contrast, the pro-haptens eugenol, isoeugenol, and 2-aminophenol stimulated high levels of IL-8 release from neutrophils alone. pro-haptens 17-28 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 23069909-5 2012 report the upregulation of IL-6 and IL-8 after the activation of the unfolded protein response (UPR) following exposure of melanocytes to phenols. Phenols 138-145 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 22841897-0 2012 1alpha,25-Dihydroxyvitamin D(3) inhibits vascular cellular adhesion molecule-1 expression and interleukin-8 production in human coronary arterial endothelial cells. Calcitriol 0-31 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 22762504-4 2012 Applied alone, RV, UV and FICZ induced time- and dose-dependent activation of aryl hydrocarbon receptor (AhR) pathway followed by over-expression of Cyp1A1 (metabolic response), UV and RV induced IL-8 expression (inflammatory response), while RV enhanced also HEK proliferation revealed by MTT assay and (3)H-thymidine incorporation. monooxyethylene trimethylolpropane tristearate 290-293 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 22762504-4 2012 Applied alone, RV, UV and FICZ induced time- and dose-dependent activation of aryl hydrocarbon receptor (AhR) pathway followed by over-expression of Cyp1A1 (metabolic response), UV and RV induced IL-8 expression (inflammatory response), while RV enhanced also HEK proliferation revealed by MTT assay and (3)H-thymidine incorporation. Thymidine 309-318 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 22927481-9 2012 Chemotaxis of CD16(bright)/CD62L(dim) neutrophils to the end-target chemoattractant N-formylmethionine-leucine-phenylalanine was lower compared with that for the CD16(dim)/CD62L(bright) neutrophil subset, whereas chemotaxis to cell-derived chemoattractant CXCL8 was comparable. N-Formylmethionine 84-102 C-X-C motif chemokine ligand 8 Homo sapiens 256-261 22927481-9 2012 Chemotaxis of CD16(bright)/CD62L(dim) neutrophils to the end-target chemoattractant N-formylmethionine-leucine-phenylalanine was lower compared with that for the CD16(dim)/CD62L(bright) neutrophil subset, whereas chemotaxis to cell-derived chemoattractant CXCL8 was comparable. leucine-phenylalanine 103-124 C-X-C motif chemokine ligand 8 Homo sapiens 256-261 22946548-5 2012 In contrast, the pro-haptens eugenol, isoeugenol, and 2-aminophenol stimulated high levels of IL-8 release from neutrophils alone. Eugenol 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 22946548-5 2012 In contrast, the pro-haptens eugenol, isoeugenol, and 2-aminophenol stimulated high levels of IL-8 release from neutrophils alone. isoeugenol 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 22946548-5 2012 In contrast, the pro-haptens eugenol, isoeugenol, and 2-aminophenol stimulated high levels of IL-8 release from neutrophils alone. 2-aminophenol 54-67 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 22721959-8 2012 Treatment of the cells with PD98059 resulted in inhibition of IL-8 mRNA expression induced by the toxin and that with SB203580 led to a decrease in the stabilization of IL-8 mRNA. SB 203580 118-126 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 22721959-7 2012 On the other hand, PD98059 and SB203580 suppressed the toxin-induced production of IL-8. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 22684779-0 2012 Polyphenon-60 displays a therapeutic effect on acne by suppression of TLR2 and IL-8 expression via down-regulating the ERK1/2 pathway. polyphenon-60 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 22684779-7 2012 We found that polyphenon-60 reduced the levels of P. acnes-enhanced TLR2 and interleukin-8 (IL-8) in THP-1 cells, human monocyte cell line and human primary monocytes. polyphenon 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 22684779-8 2012 Taken together, these data demonstrate that polyphenon-60 has a therapeutic effect on acne by suppressing inflammation, specifically by inhibiting TLR2 expression and IL-8 secretion via down-regulation of extracellular signal-regulated kinases 1/2 (ERK1/2) pathway and activator protein-1 (AP-1) pathway. polyphenon-60 44-57 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 22721959-7 2012 On the other hand, PD98059 and SB203580 suppressed the toxin-induced production of IL-8. SB 203580 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 22923236-6 2012 Neutralizing antibodies against IL-6 and IL-8 partially reversed the drug resistance of MCF-7/R to paclitaxel and doxorubicin, while a neutralizing antibody against MCP-1 had no significant effect. Paclitaxel 99-109 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 22721959-8 2012 Treatment of the cells with PD98059 resulted in inhibition of IL-8 mRNA expression induced by the toxin and that with SB203580 led to a decrease in the stabilization of IL-8 mRNA. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 28-35 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 22528769-4 2012 c-Fos methylation levels, according to the bisulfite sequencing results, were decreased in 20, 40, and 80 mg/l NaF-treated groups against the control group. hydrogen sulfite 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 22923236-6 2012 Neutralizing antibodies against IL-6 and IL-8 partially reversed the drug resistance of MCF-7/R to paclitaxel and doxorubicin, while a neutralizing antibody against MCP-1 had no significant effect. Doxorubicin 114-125 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 22622430-5 2012 However, melanoma SP cells were also resistant to temozolomide, which is not a substrate for ABC transporters, through IL-8 upregulation. Temozolomide 50-62 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 23077414-1 2012 OBJECTIVE: The aim of this study was to examine the effect of temperature on fluoride uptake by enamel specimens from a 0.05% NaF-fluoridated mouthrinse (Oral-B Advantage; Oral-B Laboratories, Newbridge, UK). Fluorides 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 126-129 23077414-6 2012 This effect was particularly noticeable at 43 C. CONCLUSIONS: The temperature of the NaF mouthrinse may easily and safely be increased beyond room temperature by placing a container of the NaF mouthrinse in a bowl of hot water, allowing greater fluoride penetration into the enamel from the mouthrinse when used at home as a routine prophylactic agent. Fluorides 245-253 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 23077414-6 2012 This effect was particularly noticeable at 43 C. CONCLUSIONS: The temperature of the NaF mouthrinse may easily and safely be increased beyond room temperature by placing a container of the NaF mouthrinse in a bowl of hot water, allowing greater fluoride penetration into the enamel from the mouthrinse when used at home as a routine prophylactic agent. Fluorides 245-253 C-X-C motif chemokine ligand 8 Homo sapiens 189-192 22762377-3 2012 While poly(I:C) induced IL-8 gene expression was solely inhibited by the NF-kappaB inhibitor III, MCP-1 gene induction was also blocked by PKA, p38 MAPK and JAK-STAT inhibitors. Poly I-C 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 22762377-6 2012 These data are indicative for distinct signalling pathways in the poly(I:C)-induced gene expression of IL-8 and MCP-1 in HaCaT keratinocytes. Poly I-C 66-75 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 22947346-6 2012 In patients with severe asthma, dexamethasone caused less suppression of CCL11 and CXCL8 release induced by TNF-alpha. Dexamethasone 32-45 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 22526597-8 2012 The decreased activation of RelA by calcitriol was confirmed by decreased release of RelA-inducible molecules, including IL-5, IL-6 and IL-8, by HBSMCs upon calcitriol treatment. Calcitriol 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 22526597-8 2012 The decreased activation of RelA by calcitriol was confirmed by decreased release of RelA-inducible molecules, including IL-5, IL-6 and IL-8, by HBSMCs upon calcitriol treatment. Calcitriol 157-167 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 22971921-6 2012 Notably, these cells are also resistant to temozolomide, which is not a substrate for ATP-Binding Cassette (ABC) transporters, in an interleukin (IL)-8-dependent manner. Temozolomide 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 133-151 22715179-11 2012 Severe vitamin D deficiency (total 25(OH)D <25 nmol/L) was associated with higher baseline TNF, IL-6, and IL-8 irrespective of IRIS status. Vitamin D 7-16 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 22441735-10 2012 H(2)O(2)-decreased NRF expression and -enhanced IL-8/CXCL8 production was augmented in COPD PBMCs. Hydrogen Peroxide 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 22441735-10 2012 H(2)O(2)-decreased NRF expression and -enhanced IL-8/CXCL8 production was augmented in COPD PBMCs. Hydrogen Peroxide 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 53-58 22888169-10 2012 MAIN FINDINGS: Using the human first trimester trophoblast cell line, HTR8, pravastatin significantly augmented, compared with no treatment, aPL-dependent secretion of interleukin (IL)-8 (P< 0.05), IL-1beta (P< 0.05) and soluble endoglin (P< 0.01) but had no effect on aPL-induced up-regulation of vascular endothelial growth factor, placenta growth factor or growth-related oncogene alpha secretion. Pravastatin 76-87 C-X-C motif chemokine ligand 8 Homo sapiens 168-186 22507555-6 2012 SIRT1 inhibition by sirtinol or Sirt1 siRNA reversed the effects of melatonin on H(2) O(2) -mediated induction of pro-inflammatory cytokines (NO, PGE(2) , TNF-alpha, IL-1beta, and IL-8) and the expression of iNOS, COX-2, and cartilage destruction molecules. Melatonin 68-77 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 22837207-7 2012 Compared to wild-type virus, NiVDeltaC induced increased expression of interleukin 1 beta (IL-1beta), IL-8, CXCL2, CXCL3, CXCL6, CCL20, and beta interferon. nivdeltac 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 22787116-10 2012 MG262 concentration-dependently inhibited basal and transforming growth factor-beta-induced collagen mRNA expression and interleukin (IL)-1beta-induced production of IL-6, IL-8, monocyte chemoattractant protein-1, regulated on activation normal T cell expressed and secreted, and granulocyte/macrophage colony-stimulating factor in both fibroblast types. MG 262 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 23046936-7 2012 The mRNA and protein expressions of both IL-8 and IP-10 were elevated significantly by the co-stimulation of LPS and 0.1 mug/mL poly (I:C) compared with control group and simple LPS groups. poly 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 22687715-6 2012 In addition, IL-8 and IL-6 levels were significantly higher in culture supernatants of A549 cells that were incubated with formaldehyde-fixed P. brasiliensis compared to cultures of cells that were infected with live yeasts. Formaldehyde 123-135 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 22752429-8 2012 We also showed that PF-04880594 stimulates production of the inflammatory cytokine interleukin 8 in HL-60 cells, suggesting a possible mechanism for the skin flushing observed in dogs. PF-04880594 20-31 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 22690903-5 2012 Only lipopolysaccharide (LPS), poly(I:C), Pam3CSK4 and MALP-2 could induce the production of IL-6, IL-8 and MCP-1 by adipocytes. Poly I 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 22690903-5 2012 Only lipopolysaccharide (LPS), poly(I:C), Pam3CSK4 and MALP-2 could induce the production of IL-6, IL-8 and MCP-1 by adipocytes. Carbon 38-39 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 23046936-8 2012 (2) The mRNA and protein expressions of IL-8 and IP-10 increased under the challenge of different concentrations of poly(I:C) (0.001, 0.01, 0.1 mug/mL) in a concentration-dependent manner, which showed no change after adding 10 mug/mL LPS. poly 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 23046936-9 2012 (3) Dexamethasone (1 mumol/L) and SB203580 (20 mumol/L) significantly decreased both the mRNA and protein production of IL-8 and IP-10 induced by co-stimulation of 0.1 mug/mL poly (I:C) and 10 mug/mL LPS compared with the control group and control+DMSO group respectively (P<0.01 and P<0.05). Dexamethasone 4-17 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 23046936-9 2012 (3) Dexamethasone (1 mumol/L) and SB203580 (20 mumol/L) significantly decreased both the mRNA and protein production of IL-8 and IP-10 induced by co-stimulation of 0.1 mug/mL poly (I:C) and 10 mug/mL LPS compared with the control group and control+DMSO group respectively (P<0.01 and P<0.05). SB 203580 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 23046936-9 2012 (3) Dexamethasone (1 mumol/L) and SB203580 (20 mumol/L) significantly decreased both the mRNA and protein production of IL-8 and IP-10 induced by co-stimulation of 0.1 mug/mL poly (I:C) and 10 mug/mL LPS compared with the control group and control+DMSO group respectively (P<0.01 and P<0.05). poly 175-179 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 23046936-9 2012 (3) Dexamethasone (1 mumol/L) and SB203580 (20 mumol/L) significantly decreased both the mRNA and protein production of IL-8 and IP-10 induced by co-stimulation of 0.1 mug/mL poly (I:C) and 10 mug/mL LPS compared with the control group and control+DMSO group respectively (P<0.01 and P<0.05). Dimethyl Sulfoxide 248-252 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 23006534-9 2012 RESULTS: Incubation with LPS, LTA or TCS significantly increased TNF-alpha, IL-1beta, IL-6, IL-8, IFN-gamma and IL-2 in comparison to incubation with RPMI alone. lipoteichoic acid 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 22902791-7 2012 Bronchoalveolar lavage CCSP and CCSP/interleukin 8 levels were low and decreasing early after transplantation in LTR who developed BOS (P=0.015). N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 23006534-9 2012 RESULTS: Incubation with LPS, LTA or TCS significantly increased TNF-alpha, IL-1beta, IL-6, IL-8, IFN-gamma and IL-2 in comparison to incubation with RPMI alone. Technetium 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 23158718-1 2012 OBJECTIVE: To evaluate the diagnostic values of (18)F-sodium fluoride ((18)F-NaF) positron emission tomography/computed tomography (PET/CT) imaging in the detection of bone metastases of lung cancer. Sodium Fluoride 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 22451299-0 2012 Resveratrol and its synthetic derivatives exert opposite effects on mesothelial cell-dependent angiogenesis via modulating secretion of VEGF and IL-8/CXCL8. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 22843691-6 2012 The induced TRPA1 channels, which were intrinsically activated by endogenous hydrogen peroxide and Zn(2+), suppressed secretion of interleukin-6 and interleukin-8. Hydrogen Peroxide 77-94 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 22843691-6 2012 The induced TRPA1 channels, which were intrinsically activated by endogenous hydrogen peroxide and Zn(2+), suppressed secretion of interleukin-6 and interleukin-8. Zinc 99-101 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 22790593-3 2012 In addition, HCl causes release of IL-8 from the esophageal mucosa. Hydrochloric Acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 22790593-6 2012 HCl upregulated mRNA and protein expression for the acid-sensing transient receptor potential cation channel, subfamily vanilloid member 1 (TRPV1), lyso-PAF AT, IL-8, eotaxin-1, -2, and -3, macrophage inflammatory protein-1alpha, and monocyte chemoattractant protein-1. Hydrochloric Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 22790593-8 2012 In HET-1A cells, the TRPV1 agonist capsaicin reproduced these findings for mRNA of the inflammatory mediators lyso-PAF AT, IL-8, and eotaxin-1. Capsaicin 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 22451299-0 2012 Resveratrol and its synthetic derivatives exert opposite effects on mesothelial cell-dependent angiogenesis via modulating secretion of VEGF and IL-8/CXCL8. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 150-155 22451299-4 2012 This effect was associated with decreased secretion of VEGF and IL-8/CXCL8 by HPMCs treated with RVT, which confirmed the experiments with recombinant forms of these angiogenic agents. Hypromellose Derivatives 78-83 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 22451299-4 2012 This effect was associated with decreased secretion of VEGF and IL-8/CXCL8 by HPMCs treated with RVT, which confirmed the experiments with recombinant forms of these angiogenic agents. Hypromellose Derivatives 78-83 C-X-C motif chemokine ligand 8 Homo sapiens 69-74 22549761-11 2012 Mitochondrial dysfunction increased the chemotactic activity induced by cytokines, and ROS and NF-kappaB inhibitors decreased the production of IL-8. Reactive Oxygen Species 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 22684025-5 2012 Among the four families of oxPS studied, only oxPS modified in the polar head with formation of a terminal hydroperoxyacetaldehyde upregulated the production of cytokines IL-8 and TNF-alpha by monocytes and DCs subsets (mDCs and CD14(-/low)CD16(+) DCs). Hydroperoxyacetaldehyde 107-130 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 22971256-7 2012 The brackets in group 4 were bonded with Transbond Plus self-etching primer, and group 5 underwent treatment with a 2% sodium fluoride (NaF) gel, which was applied on the enamel surface for 4 minutes before etching. Sodium Fluoride 119-134 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 22796581-8 2012 Simvastatin significantly reduced plasma troponin T, isoenzyme of creatine kinase, C-reaction protein, blood urea nitrogen , creatinine, interleukin-6, interleukin-8, and the requirement of inotropic postoperatively. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 152-165 22925316-4 2012 The mechanism(s) of action of macrolides in the treatment of these diseases remains unexplained, but may be due to their antibacterial and/or anti-inflammatory actions, which include reductions in interleukin-8 production, neutrophil migration and/or function. Macrolides 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 197-210 22542524-17 2012 crispatus K243 and K313 inhibited the IL-8 secretion triggered by S. braenderup H9812 by 32.8% and 47.0%, indicating that the two isolates could attenuate the pro-inflammatory signaling induced by S. braenderup H9812, and have the potential application in clinical practice to prevent diarrhea. palladium chloride 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 22248218-2 2012 The purpose of this study is to determine whether there are subpopulations of peripheral neutrophils in patients with chronic periodontitis (CP) that generate different levels of intracellular ROS when primed with tumor necrosis factor-alpha (TNF-alpha) or the chemokine interleukin-8 (IL-8, CXCL8) compared to controls. Reactive Oxygen Species 193-196 C-X-C motif chemokine ligand 8 Homo sapiens 286-290 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. Adenosine Triphosphate 66-91 C-X-C motif chemokine ligand 8 Homo sapiens 238-243 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. Adenosine Triphosphate 66-91 C-X-C motif chemokine ligand 8 Homo sapiens 245-258 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. Adenosine Triphosphate 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 238-243 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. Adenosine Triphosphate 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 245-258 22743248-7 2012 We demonstrated that treatment of A375 cells with IS in combination with paclitaxel resulted in a significant decrease in the production of IL-8 and VEGF, compared with paclitaxel alone. Paclitaxel 73-83 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 22618201-6 2012 The p38 inhibitor SB203580 and the STAT1 inhibitor EGCG blocked CM-induced IL-8 production at both early and late time periods. SB 203580 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 22618201-6 2012 The p38 inhibitor SB203580 and the STAT1 inhibitor EGCG blocked CM-induced IL-8 production at both early and late time periods. epigallocatechin gallate 51-55 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 22618201-7 2012 The NF-kappaB inhibitors PDTC and BAY11-7082 were found to increase CM-stimulated IL-8 production in Caco-2 cells at 24 h. CONCLUSIONS: Our data suggest an effective strategy to reduce IL-8 production is to block p38 or STAT1 rather than NF-kappaB. 3-(4-methylphenylsulfonyl)-2-propenenitrile 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 22618201-7 2012 The NF-kappaB inhibitors PDTC and BAY11-7082 were found to increase CM-stimulated IL-8 production in Caco-2 cells at 24 h. CONCLUSIONS: Our data suggest an effective strategy to reduce IL-8 production is to block p38 or STAT1 rather than NF-kappaB. 3-(4-methylphenylsulfonyl)-2-propenenitrile 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 23023382-6 2012 RESULTS: BSO and NAC significantly decreased IL-6 and TNF-alpha levels at 14 days of differentiation, whereas, NAC decreased the levels of IL-8 at days 2 and 14 of differentiation. nac 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 22105830-10 2012 In addition, linoleic acid but not oleic acid induced MSC to increase production of interleukin-8. Linoleic Acid 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 22105830-10 2012 In addition, linoleic acid but not oleic acid induced MSC to increase production of interleukin-8. Oleic Acid 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 22320379-5 2012 RESULTS: The findings show that interleukin concentrations (IL-6, IL-8, TNF-alpha) were significantly decreased between 0 and 72 hours (p < 0.01) in the newborns exposed to initial oxygen concentration of 45% and significantly increased in the other group. Oxygen 184-190 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. adenosine 5'-O-(3-thiotriphosphate) 102-138 C-X-C motif chemokine ligand 8 Homo sapiens 238-243 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. adenosine 5'-O-(3-thiotriphosphate) 102-138 C-X-C motif chemokine ligand 8 Homo sapiens 245-258 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. adenosine 5'-O-(3-thiotriphosphate) 140-149 C-X-C motif chemokine ligand 8 Homo sapiens 238-243 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. adenosine 5'-O-(3-thiotriphosphate) 140-149 C-X-C motif chemokine ligand 8 Homo sapiens 245-258 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. Adenosine Triphosphate 140-143 C-X-C motif chemokine ligand 8 Homo sapiens 238-243 22897577-6 2012 We have previously shown that the sympathetic nerve cotransmitter adenosine-5"-triphosphate (ATP) and adenosine-5"-O-(3-thio) triphosphate (ATPgammaS), an ATP analogue that is resistant to hydrolysis, increase secretion of the chemokines CXCL8 (interleukin-8), CCL2 (monocyte chemotactic protein-1) and CXCL1 (growth-regulated oncogene alpha) by dermal microvascular ECs. Adenosine Triphosphate 140-143 C-X-C motif chemokine ligand 8 Homo sapiens 245-258 22897577-8 2012 We have now demonstrated that AFC dose-dependently inhibits ATP-, ATPgammaS- and TNFalpha-induced production of CXCL1, CXCL8 and CCL2 by a human dermal microvascular EC line (HMEC-1) in vitro under conditions that do not affect cell viability. Adenosine Triphosphate 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 119-124 22897577-8 2012 We have now demonstrated that AFC dose-dependently inhibits ATP-, ATPgammaS- and TNFalpha-induced production of CXCL1, CXCL8 and CCL2 by a human dermal microvascular EC line (HMEC-1) in vitro under conditions that do not affect cell viability. adenosine 5'-O-(3-thiotriphosphate) 66-75 C-X-C motif chemokine ligand 8 Homo sapiens 119-124 22710663-5 2012 We demonstrated that 4,8-SD significantly inhibited tumor necrosis factor-alpha (TNF-alpha)- and lipopolysaccharide (LPS)-induced expression of IL-8 and E-selectin in human endothelial cells in a dose-dependent manner. 4,8-sd 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 22248218-2 2012 The purpose of this study is to determine whether there are subpopulations of peripheral neutrophils in patients with chronic periodontitis (CP) that generate different levels of intracellular ROS when primed with tumor necrosis factor-alpha (TNF-alpha) or the chemokine interleukin-8 (IL-8, CXCL8) compared to controls. Reactive Oxygen Species 193-196 C-X-C motif chemokine ligand 8 Homo sapiens 271-284 22248218-2 2012 The purpose of this study is to determine whether there are subpopulations of peripheral neutrophils in patients with chronic periodontitis (CP) that generate different levels of intracellular ROS when primed with tumor necrosis factor-alpha (TNF-alpha) or the chemokine interleukin-8 (IL-8, CXCL8) compared to controls. Reactive Oxygen Species 193-196 C-X-C motif chemokine ligand 8 Homo sapiens 292-297 22751949-6 2012 A degradation product of thymidine was implicated in the enhanced expression of IL-8. Thymidine 25-34 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 22751949-8 2012 An antioxidant, N-acetylcysteine (NAC), attenuated the generation of ROS and IL-8 mRNA expression in KB and Yumoto cells, and H2O2 increased IL-8 mRNA expression in Yumoto cells, suggesting that ROS generated by TP caused the increased expression of IL-8 mRNA. Acetylcysteine 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 22527530-6 2012 To avoid dilution effects, urinary levels of IL-6 and IL-8 were expressed as the ratio of cytokine to urinary creatinine (pg/mg). Creatinine 110-120 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 22751949-8 2012 An antioxidant, N-acetylcysteine (NAC), attenuated the generation of ROS and IL-8 mRNA expression in KB and Yumoto cells, and H2O2 increased IL-8 mRNA expression in Yumoto cells, suggesting that ROS generated by TP caused the increased expression of IL-8 mRNA. Acetylcysteine 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 22751949-8 2012 An antioxidant, N-acetylcysteine (NAC), attenuated the generation of ROS and IL-8 mRNA expression in KB and Yumoto cells, and H2O2 increased IL-8 mRNA expression in Yumoto cells, suggesting that ROS generated by TP caused the increased expression of IL-8 mRNA. Acetylcysteine 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 22751949-8 2012 An antioxidant, N-acetylcysteine (NAC), attenuated the generation of ROS and IL-8 mRNA expression in KB and Yumoto cells, and H2O2 increased IL-8 mRNA expression in Yumoto cells, suggesting that ROS generated by TP caused the increased expression of IL-8 mRNA. Acetylcysteine 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 22751949-8 2012 An antioxidant, N-acetylcysteine (NAC), attenuated the generation of ROS and IL-8 mRNA expression in KB and Yumoto cells, and H2O2 increased IL-8 mRNA expression in Yumoto cells, suggesting that ROS generated by TP caused the increased expression of IL-8 mRNA. Hydrogen Peroxide 138-142 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 22751949-8 2012 An antioxidant, N-acetylcysteine (NAC), attenuated the generation of ROS and IL-8 mRNA expression in KB and Yumoto cells, and H2O2 increased IL-8 mRNA expression in Yumoto cells, suggesting that ROS generated by TP caused the increased expression of IL-8 mRNA. Hydrogen Peroxide 138-142 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 22751949-10 2012 Our findings suggest that thymidine-derived sugars enhanced ROS generation and consequently increased IL-8 expression. Sugars 56-62 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 23157890-6 2012 The median of levels of IL-8 among the unexposed controls was 207.34 pg/ml, which was significantly higher than that among the TCE-exposed workers (28.26 pg/ml, P < 0.01). Trichloroethylene 127-130 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 22525295-7 2012 The proliferation of EBf-H9 and murine L929 cells was inhibited by sodium fluoride (NaF) and formaldehyde (FA), and the cell cycle was arrested in different phases with the treatments. Sodium Fluoride 67-82 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 22909087-7 2012 The DMSO-soluble component curcumin, whose occurrence within the DMSO extract was verified by HPLC/MS, reduced levels of IL-1beta, IL-6, IL-8, MMP1, MMP3 and MMP13 and both caused an up-regulation of TNF-alpha. Dimethyl Sulfoxide 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 22909087-7 2012 The DMSO-soluble component curcumin, whose occurrence within the DMSO extract was verified by HPLC/MS, reduced levels of IL-1beta, IL-6, IL-8, MMP1, MMP3 and MMP13 and both caused an up-regulation of TNF-alpha. Curcumin 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 22909087-7 2012 The DMSO-soluble component curcumin, whose occurrence within the DMSO extract was verified by HPLC/MS, reduced levels of IL-1beta, IL-6, IL-8, MMP1, MMP3 and MMP13 and both caused an up-regulation of TNF-alpha. Dimethyl Sulfoxide 65-69 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 22867088-15 2012 In addition, pretreatment of HBEC with the antioxidant N-acetyl cysteine significantly inhibited DEP-induced ERK and Akt phosphorylation, and subsequent IL-8 and IL-1beta expression. Acetylcysteine 55-72 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 21964883-8 2012 Finally, we evaluated the regulation pathways involved in LPA-induced IL-8 expression. lysophosphatidic acid 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 22841385-7 2012 Exposure of mdDC to purified CarLA resulted in the increased production of the pro-inflammatory cytokines IL-6 and to a lesser extent of IL-8 and TNF-alpha, and a reduced production of the anti-inflammatory cytokine IL-1RA. mddc 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 22891766-5 2012 In this novel mechanism, TWIST1-mediated IL8 transcription is induced through the TWIST1 carboxy-terminal WR (Trp-Arg) domain instead of the classic DNA binding bHLH domain. Tryptophan 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 22891766-5 2012 In this novel mechanism, TWIST1-mediated IL8 transcription is induced through the TWIST1 carboxy-terminal WR (Trp-Arg) domain instead of the classic DNA binding bHLH domain. Arginine 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 22883023-8 2012 Serum levels of IL6 and IL8 also increased in the arsenic exposed group. Arsenic 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 22634165-9 2012 Our results showed that splitomicin inhibited superoxide anion production by fMLP (1 muM) and NaF (20mM) in a concentration-dependent manner (37.5-450 muM). splitomicin 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 22634165-9 2012 Our results showed that splitomicin inhibited superoxide anion production by fMLP (1 muM) and NaF (20mM) in a concentration-dependent manner (37.5-450 muM). Superoxides 46-62 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 22867088-15 2012 In addition, pretreatment of HBEC with the antioxidant N-acetyl cysteine significantly inhibited DEP-induced ERK and Akt phosphorylation, and subsequent IL-8 and IL-1beta expression. dep 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 22661653-8 2012 Quercetin reduced IL-6, IL-8 and TNFalpha protein production in supernatants of all GO samples (n=4) in a dose-dependent manner; however, only the reduction in IL-6 was statistically significant (p<0.05). Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 22427536-7 2012 Studies performed using BEAS-2B cells showed that pretreatment with heparin and syndecan-4 decreased the expression of CXCL8 mRNA in response to LPS and TNF-alpha. Heparin 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 119-124 22523282-5 2012 The role of TAK1 in CS-induced IL-8 release is not known. Cesium 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 22523282-7 2012 Stimulation of these cells with CS extract (CSE) increased IL-8 release and ERK-1/2 phosphorylation, as well as Ikappa-Balpha degradation and p65 NF-kappaB subunit phosphorylation. Cesium 32-34 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 22579587-2 2012 The carrageenan-induced inflammatory cascades involve toll-like receptor (TLR)4- and B-cell leukemia/lymphoma (BCL)10-dependent activation of NF-kappaB, leading to increased IL-8 production. Carrageenan 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 22579587-7 2012 Prolonged inflammation follows activation of the BCL10-NFkappaB inflammatory loop in response to carrageenan, shown by increased BCL10, RelA, and IL-8 for 36 to 48h and increased RelB for 24h following withdrawal of carrageenan after 12h. Carrageenan 97-108 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 22300324-7 2012 KEY RESULTS: TGF-beta (40-400 pM) reduced the maximum inhibitory effect of dexamethasone on IL-1alpha-induced IL-6 and CXCL8 production. Dexamethasone 75-88 C-X-C motif chemokine ligand 8 Homo sapiens 119-124 22661653-9 2012 Quercetin had a significant suppression of tissue IL-6, IL-8, IL-1beta and TNFalpha mRNA expression in cultured orbital tissues from three GO samples relative to untreated control tissue (p<0.05). Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 21750917-1 2012 The aim of this study was to evaluate the remineralization potential of three silica-containing NaF dentifrice systems in an intraoral model. Silicon Dioxide 78-84 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 22578660-3 2012 Two sodium fluoride (NaF) solutions at 10% and 3% were prepared, and they had the same fluoride ion concentrations as 38% and 12% SDF, respectively. Sodium Fluoride 4-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 22578660-3 2012 Two sodium fluoride (NaF) solutions at 10% and 3% were prepared, and they had the same fluoride ion concentrations as 38% and 12% SDF, respectively. Fluorides 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 22583692-7 2012 Logistic regression analysis demonstrated a significant positive association between PTU and high levels of IFN-gamma, IL-8, MIG and IP-10. ptu 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 22728263-1 2012 UNLABELLED: We evaluated the kinetics of (18)F-sodium fluoride (NaF) and reassessed the recommended dose, optimal uptake period, and reproducibility using a current-generation PET/CT scanner. Sodium Fluoride 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 22641358-7 2012 We found that IL-1Ra and EGCG downregulated IL-1-induced IL-6 and IL-8 release from U-2 OS cells by 65-85%. epigallocatechin gallate 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 22687252-8 2012 In addition, KOB03 inhibited the production of inflammatory cytokines such as TNF-alpha, IL-1beta, IL-6 and IL-8 in PMA/A23187-stimulated HMC-1 mast cells by suppressing their gene expression and blocking the ERK1/2 and p38 MAPK and NF-kappaB pathways. Calcimycin 120-126 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 22775995-5 2012 The COL17-deficient cells showed an abnormally high IL-8 response after treatment with lipopolysaccharide (LPS), ultraviolet-B radiation or tumor necrosis factor, but exhibited a blunted IL-8 response to phorbol 12-myristate 13-acetate exposure. Tetradecanoylphorbol Acetate 204-235 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 22527144-5 2012 Moreover, pretreatment with apigenin partially inhibited the DEHP-induced activation of c-Jun N-terminal kinase (JNK) but not the degradation of IkappaBalpha or the phosphorylation of extracellular-regulated kinase (ERK)1/2, indicating that the inhibitory effect of apigenin on the expression of IL-6, IL-8, and ICAM-1 may be mediated by JNK pathway but not IkappaBalpha/nuclear factor-kappaB or ERK/mitogen-activated protein kinase pathway. Apigenin 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 302-306 22759480-8 2012 Confirmatory analyses identified associations of interleukin 6, interleukin 8, VEGF, osteopontin, E-selectin, and HGF with continuous tumour shrinkage or PFS in patients treated with pazopanib. pazopanib 183-192 C-X-C motif chemokine ligand 8 Homo sapiens 64-77 22577802-8 2012 Imiquimod induced IL-6 and IL-8 production in OSCC cells, suggesting the functional expression of TLR7. Imiquimod 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 22759480-9 2012 In the validation set of samples from the phase 3 trial, patients treated with pazopanib who had high concentrations (relative to median) of interleukin 8 (p=0 006), osteopontin (p=0 0004), HGF (p=0 010), and TIMP-1 (p=0 006) had shorter PFS than did those with low concentrations. pazopanib 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 141-154 22812506-5 2012 The antioxidant Trolox in part prevented the detrimental effect of NMs on cell viability, and decreased the NM induced IL8 production after exposure to all but the Ag particulate. 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid 16-22 C-X-C motif chemokine ligand 8 Homo sapiens 119-122 22849850-9 2012 The release of IL-8 was inhibited by the NF-kappaB inhibitor, caffeic acid phenethyl ester (CAPE), an inhibitor of nuclear factor kappa-B alpha (IkappaBalpha) inhibitor, BAY 11-7085, and an inhibitor of nuclear factor kappa-B kinase-2 (IKK-2) inhibitor, SC-514, but not by a c-Jun N-terminal kinase (JNK) inhibitory peptide, L-JNKi1. caffeic acid phenethyl ester 62-90 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 22849850-9 2012 The release of IL-8 was inhibited by the NF-kappaB inhibitor, caffeic acid phenethyl ester (CAPE), an inhibitor of nuclear factor kappa-B alpha (IkappaBalpha) inhibitor, BAY 11-7085, and an inhibitor of nuclear factor kappa-B kinase-2 (IKK-2) inhibitor, SC-514, but not by a c-Jun N-terminal kinase (JNK) inhibitory peptide, L-JNKi1. caffeic acid phenethyl ester 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 22849850-9 2012 The release of IL-8 was inhibited by the NF-kappaB inhibitor, caffeic acid phenethyl ester (CAPE), an inhibitor of nuclear factor kappa-B alpha (IkappaBalpha) inhibitor, BAY 11-7085, and an inhibitor of nuclear factor kappa-B kinase-2 (IKK-2) inhibitor, SC-514, but not by a c-Jun N-terminal kinase (JNK) inhibitory peptide, L-JNKi1. BAY 11-7085 170-181 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 22849850-9 2012 The release of IL-8 was inhibited by the NF-kappaB inhibitor, caffeic acid phenethyl ester (CAPE), an inhibitor of nuclear factor kappa-B alpha (IkappaBalpha) inhibitor, BAY 11-7085, and an inhibitor of nuclear factor kappa-B kinase-2 (IKK-2) inhibitor, SC-514, but not by a c-Jun N-terminal kinase (JNK) inhibitory peptide, L-JNKi1. SC 514 254-260 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 22849850-10 2012 25-HC significantly potentiated IL-8 release in poly(I:C)-treated cells and the augmentation was inhibited by CAPE, BAY 11-7085, and SC-514. -hc 2-5 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 22849850-10 2012 25-HC significantly potentiated IL-8 release in poly(I:C)-treated cells and the augmentation was inhibited by CAPE, BAY 11-7085, and SC-514. Poly I 48-54 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 22849850-10 2012 25-HC significantly potentiated IL-8 release in poly(I:C)-treated cells and the augmentation was inhibited by CAPE, BAY 11-7085, and SC-514. Carbon 55-57 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 22411631-5 2012 The specific mitogen-activated protein kinase kinase/ERK inhibitor, U0126, blocks N. fowleri-mediated AP-1 activation and subsequent IL-8 induction. U 0126 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 22546485-7 2012 RESULTS: Both long-acting beta(2) agonists, salmeterol and formoterol, and corticosteroids, fluticasone and budesonide, showed anti-inflammatory effects to a certain extent on H(2)O(2)-induced IL-8 and MMP-9 release in alveolar macrophages. Fluticasone 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 22546485-7 2012 RESULTS: Both long-acting beta(2) agonists, salmeterol and formoterol, and corticosteroids, fluticasone and budesonide, showed anti-inflammatory effects to a certain extent on H(2)O(2)-induced IL-8 and MMP-9 release in alveolar macrophages. Budesonide 108-118 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 22609641-3 2012 Benzylpenicillin and phenoxymethylpenicillin were recognized as sensitizing compounds because they are capable to induce the mRNA expression of these genes in moDCs and, except for IL-8, in THP-1 cells but not in MUTZ-LC. Penicillin G 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 22609641-3 2012 Benzylpenicillin and phenoxymethylpenicillin were recognized as sensitizing compounds because they are capable to induce the mRNA expression of these genes in moDCs and, except for IL-8, in THP-1 cells but not in MUTZ-LC. Penicillin V 21-44 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 22444322-6 2012 In addition, the influence of long-chain hyaluronan, chondroitin sulfate, and heparin on IL-8-induced chemotaxis and oxidative activity of neutrophils was examined. Heparin 78-85 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 22444322-0 2012 The influence of glycosaminoglycans on IL-8-mediated functions of neutrophils. Glycosaminoglycans 17-35 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 22816782-3 2012 The migration patterns for individual cells were tracked and quantitatively analyzed, and the results suggest a hierarchy among these chemoattractants of fMLP > CXCL8 > CXCL2 > leukotriene B(4). Leukotrienes 186-197 C-X-C motif chemokine ligand 8 Homo sapiens 164-169 22444322-7 2012 Only the incubation of heparin with IL-8 affected the IL-8-mediated chemotaxis of neutrophils. Heparin 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 22444322-7 2012 Only the incubation of heparin with IL-8 affected the IL-8-mediated chemotaxis of neutrophils. Heparin 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 22444322-4 2012 Here, we investigated the interaction of heparin hexasaccharides and recombinant human IL-8, consisting of 77 amino acids using fluorescence and NMR spectroscopy. heparin hexasaccharides 41-64 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 22444322-8 2012 However, all investigated GAGs enhanced the IL-8-induced formation of reactive oxygen species in neutrophils, which is an entirely new finding. Reactive Oxygen Species 70-93 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 24049649-5 2012 Nevertheless, several parameters participating in oxidative stress (increased ROS production and apoptosis, decreased total thiol content) were observed in IB3-1 cells cultured in hypertonic environment as compared to S9 cells and were inhibited by diphenyleneiodonium (DPI), a well-known inhibitor of NOXs; besides, increased production of the proinflammatory cytokines IL-6 and IL-8 by IB3-1 cells was also inhibited by DPI as compared to S9 cells. diphenyleneiodonium 249-268 C-X-C motif chemokine ligand 8 Homo sapiens 380-384 22020623-7 2012 Therefore, development of specific or multi-targeted inhibitors for these kinases for combinatorial therapy with e.g., an IL-8 neutralizing antibody might circumvent or substantially delay Sunitinib resistance formation and enhance survival prognosis. Sunitinib 189-198 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 22364122-5 2012 In particular, a glucose-lysine (Glu-Lys) mixture heated for 60 min had marked intracellular antioxidant activity and nitric oxide (NO) and interleukin-8 (IL-8) inhibitory activities compared to other MRPs (P < 0.05). glucose-lysine 17-31 C-X-C motif chemokine ligand 8 Homo sapiens 140-153 22364122-5 2012 In particular, a glucose-lysine (Glu-Lys) mixture heated for 60 min had marked intracellular antioxidant activity and nitric oxide (NO) and interleukin-8 (IL-8) inhibitory activities compared to other MRPs (P < 0.05). glucose-lysine 17-31 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 22364122-5 2012 In particular, a glucose-lysine (Glu-Lys) mixture heated for 60 min had marked intracellular antioxidant activity and nitric oxide (NO) and interleukin-8 (IL-8) inhibitory activities compared to other MRPs (P < 0.05). Glutamic Acid 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 140-153 22364122-5 2012 In particular, a glucose-lysine (Glu-Lys) mixture heated for 60 min had marked intracellular antioxidant activity and nitric oxide (NO) and interleukin-8 (IL-8) inhibitory activities compared to other MRPs (P < 0.05). Glutamic Acid 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 22364122-5 2012 In particular, a glucose-lysine (Glu-Lys) mixture heated for 60 min had marked intracellular antioxidant activity and nitric oxide (NO) and interleukin-8 (IL-8) inhibitory activities compared to other MRPs (P < 0.05). Lysine 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 140-153 22364122-5 2012 In particular, a glucose-lysine (Glu-Lys) mixture heated for 60 min had marked intracellular antioxidant activity and nitric oxide (NO) and interleukin-8 (IL-8) inhibitory activities compared to other MRPs (P < 0.05). Lysine 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 22364122-7 2012 F3 inhibited NO, inducible nitric oxide synthetase (iNOS), and IL-8 in interferon gamma (IFN-gamma)- and phorbol ester (PMA)-induced Caco-2 cells. Tetradecanoylphorbol Acetate 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 22517618-5 2012 Using selective EP receptor agonists and a selective EP(4) antagonist, we show that PGE(2) mediates the repression of IL-1beta-induced release of CXCL8, CCL2, and CSF2 via activation of the EP(2) and EP(4) receptors. Prostaglandins E 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 146-151 24049649-6 2012 Furthermore, calcium ionophore (A23187), which upregulates DUOX and NOX2 activities, strongly induced oxidative stress and IL-8 and IL-6 overexpression in IB3-1 cells. Calcium 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 24049649-6 2012 Furthermore, calcium ionophore (A23187), which upregulates DUOX and NOX2 activities, strongly induced oxidative stress and IL-8 and IL-6 overexpression in IB3-1 cells. Calcimycin 32-38 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 22407301-9 2012 A dramatic loss of immunoreactive IL-8 was observed for only one of the three TiO2 particle types tested. titanium dioxide 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 22620679-11 2012 The effect of exosomes to promote LTC(4) and IL-8 release in BEC was significantly increased for exosomes from asthmatics, and the CysLT(1) receptor antagonist Montelukast reduced exosome-induced IL-8 secretion. montelukast 160-171 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 22964618-2 2012 This enzyme deficiency results in an accumulation of sphingolipids in the cells of GD patients, which may contribute to the dysregulation of the immune system, B-cell dysfunction and expression of specific cytokines such as interleukin (IL) -1, IL-6, IL-8, IL-10, and tumor necrosis factor (TNF). Sphingolipids 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 22547109-10 2012 We further showed that RO429097 inhibits normal T-cell synthesis of some inflammatory cytokines, including TNF-alpha, a potential mediator of IL-6 and IL-8 production in the microenvironment. ro429097 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 23507865-4 2012 Regulatory aspects of the interplay between IL-8 and heparan sulfate, the most abundant glycosaminoglycan, are highlighted. Glycosaminoglycans 88-105 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 23507865-5 2012 In this field, the large natural heterogeneity of glycosaminoglycans represents a great challenge that impedes the modeling of IL-8 functions. Glycosaminoglycans 50-68 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 23507865-6 2012 The interaction of IL-8 with newly developed artificial sulfated hyaluronan derivatives is also considered as these artificial substrates are an important tool for development of new materials in regenerative medicine. Hyaluronic Acid 65-75 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 22543056-7 2012 TLR3-induced TSLP, TNFalpha, CXCL8, and IFNbeta mRNA and protein levels were dose-dependently and non-selectively inhibited by capsazepine, equally in cells from asthmatic and COPD donors. capsazepine 127-138 C-X-C motif chemokine ligand 8 Homo sapiens 29-34 22610073-11 2012 Further, IL-8-promoted migration and invasion could be abolished by either the application of the phosphoinositide-3-kinase inhibitor LY294002 or the knock down of AKT expression by using small-interfering RNA. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 23121969-0 2012 Regulation of Salmonella flagellin-induced interleukin-8 in intestinal epithelial cells by muramyl dipeptide. Dipeptides 99-108 C-X-C motif chemokine ligand 8 Homo sapiens 43-56 23121969-4 2012 Therefore the aim of the study is to investigate regulation of Salmonella flagellin-induced interleukin (IL)-8 (IL-8) in IECs by Nod2 agonist, muramyl dipeptide (MDP). Acetylmuramyl-Alanyl-Isoglutamine 143-160 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 23121969-4 2012 Therefore the aim of the study is to investigate regulation of Salmonella flagellin-induced interleukin (IL)-8 (IL-8) in IECs by Nod2 agonist, muramyl dipeptide (MDP). Acetylmuramyl-Alanyl-Isoglutamine 162-165 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 22437006-4 2012 However, both HKVC and the LPS showed a substantial induction of IL-8 production in IFN-gamma-primed HT-29 cells. hkvc 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 22626465-0 2012 Astaxanthin attenuates the UVB-induced secretion of prostaglandin E2 and interleukin-8 in human keratinocytes by interrupting MSK1 phosphorylation in a ROS depletion-independent manner. astaxanthine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 22626465-1 2012 To elucidate the effects of redox balance regulation on cutaneous inflammation, we used the potent antioxidant astaxanthin (AX) to assess its effect on the UVB-induced secretion of PGE(2) and IL-8 in human keratinocytes and analysed its biological mechanism of action. astaxanthine 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 22626465-9 2012 This may be associated with the significant suppression of PGE(2) /IL-8 secretion via the down-regulated expression of COX-2 and IL-8 at the gene and/or protein levels. Prostaglandins E 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 22626465-9 2012 This may be associated with the significant suppression of PGE(2) /IL-8 secretion via the down-regulated expression of COX-2 and IL-8 at the gene and/or protein levels. Prostaglandins E 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 21968713-4 2012 Both normal and immortalized human gingival epithelial (HOK-16B) cells expressed TLR9 intracellularly and showed enhanced IL-8 expression in response to CpG-oligonucleotide. CPG-oligonucleotide 153-172 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 22561123-0 2012 Corilagin is a potent inhibitor of NF-kappaB activity and downregulates TNF-alpha induced expression of IL-8 gene in cystic fibrosis IB3-1 cells. corilagin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 22561123-5 2012 The data obtained demonstrate that corilagin binds to NF-kappaB, inhibits NF-kappaB/DNA interactions and affects IL-8 gene expression in TNF-alpha treated IB3-1 cells. corilagin 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 22543056-9 2012 Only capsazepine consistently inhibited TNFalpha and CXCL8 production and attenuated TLR3-induced epithelial NF-kappaB signalling. capsazepine 5-16 C-X-C motif chemokine ligand 8 Homo sapiens 53-58 22538414-3 2012 Amphotericin B alone elicited a slight increase in interleukin (IL)-6 and IL-8 production by human gingival fibroblasts. Amphotericin B 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 22538414-4 2012 However, amphotericin B synergistically up-regulated lipid A-induced production of IL-6 and IL-8. Amphotericin B 9-23 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 22538414-4 2012 However, amphotericin B synergistically up-regulated lipid A-induced production of IL-6 and IL-8. Lipid A 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 22211698-0 2012 Interleukin-17- and protease-activated receptor 2-mediated production of CXCL1 and CXCL8 modulated by cyclosporine A, vitamin D3 and glucocorticoids in human keratinocytes. Cyclosporine 102-116 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 22538414-6 2012 Pre-treatment with methyl-beta-cyclodextrin (MbetaCD), a cholesterol-binding agent, reduced IL-6 and IL-8 production in human gingival fibroblasts. methyl-beta-cyclodextrin 19-43 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 22211698-0 2012 Interleukin-17- and protease-activated receptor 2-mediated production of CXCL1 and CXCL8 modulated by cyclosporine A, vitamin D3 and glucocorticoids in human keratinocytes. Cholecalciferol 118-128 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 22211698-4 2012 The SLIGKV-NH(2) -induced production of both CXCL1 and CXCL8 was markedly reduced by cyclosporine A. Cyclosporine 85-99 C-X-C motif chemokine ligand 8 Homo sapiens 55-60 22538414-6 2012 Pre-treatment with methyl-beta-cyclodextrin (MbetaCD), a cholesterol-binding agent, reduced IL-6 and IL-8 production in human gingival fibroblasts. methyl-beta-cyclodextrin 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 22562653-8 2012 Pretreatment with DHT inhibited NF-kappaB activation and suppressed secretion of several inflammatory/growth factors, with the most pronounced effects on IL8, IL6, and bFGF. Dihydrotestosterone 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 154-157 22460770-11 2012 Asymmetric dimethylarginine was inversely correlated with organ dysfunction by Pediatric Logistic Organ Dysfunction score (r = -0.50, p = .009), interleukin-6 (r = -0.55, p = .01), and interleukin-8 (r = -0.52, p = .03) on admission. dimethylarginine 11-27 C-X-C motif chemokine ligand 8 Homo sapiens 185-198 22425623-10 2012 The ER accumulation of Z-AT was shown to induce PERK-dependent NF-kappaB, IL-6, IL-8, and RGS16 and calnexin; all of which could be abrogated effectively by 4M. z-at 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 22512945-4 2012 COS induced up-regulation of a total of 11 genes including CCL20 and IL8 and concurrent down-regulation of 10 genes including pro-inflammatory mediators CCL15, CCL25 and IL1B. oligochitosan 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 22520513-3 2012 The action of glutamate on the secretion of IL-8 and IL-10 by lymphocytes derived from healthy subjects and cystic CF patients, as well as the expression of metabotropic glutamate receptor subtype 1 (mGluR1) in the membrane fractions of lymphocytes was investigated. Glutamic Acid 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 22183741-7 2012 In addition, treatment of endometriotic stromal cells with curcumin markedly inhibited TNF-alpha-induced secretion of IL-6, IL-8 and MCP-1. Curcumin 59-67 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 22313893-11 2012 Additionally, we also found that 25-OH decreases the levels of IkappaB and increases the nuclear levels of NF-kappaB p65 subunit and that inhibition of NF-kappaB activity partially prevents the increased secretion of IL-8 induced by 25-OH. 25-oh 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 27157456-2 2012 (18)F-labeled sodium fluoride (NaF) PET with computed tomography (PET/CT) is a promising tool for the evaluation of benign bone disease. Sodium Fluoride 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 27157457-2 2012 (18)F-Labeled sodium fluoride ((18)F NaF) is a positron-emitting radiopharmaceutical with desirable characteristics (rapid blood clearance and bone uptake) for high-quality functional imaging of the skeleton. Sodium Fluoride 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 27157459-1 2012 Skeletal imaging of children with fluorine-18 ((18)F) NaF harnesses the superior imaging characteristics of positron emission tomography (PET) and the improved biodistribution of the fluoride tracer compared with standard nuclear techniques, resulting in excellent quality images. Fluorine 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 27157459-1 2012 Skeletal imaging of children with fluorine-18 ((18)F) NaF harnesses the superior imaging characteristics of positron emission tomography (PET) and the improved biodistribution of the fluoride tracer compared with standard nuclear techniques, resulting in excellent quality images. Fluorides 183-191 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 27157462-1 2012 Detection of early ongoing cardiovascular molecular calcification and its quantification through (18)F-labeled sodium fluoride ((18)F NaF) PET/computed tomography (CT) imaging has been a recent addition to the diagnostic armamentarium of molecular imaging for the atherosclerotic process. Sodium Fluoride 111-126 C-X-C motif chemokine ligand 8 Homo sapiens 134-137 22012204-12 2012 The levels of IL-6 and IL-8 were significantly reduced at 4 weeks after intravitreal MTX, whereas those of vascular endothelial growth factor and monocyte chemotactic protein 1 were not reduced. Methotrexate 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 22012204-14 2012 Intravitreal MTX was associated with a significant reduction of IL-6 and IL-8 levels and was effective and well tolerated even in steroid responders with refractory retinal vasculitis due to Behcet disease. Methotrexate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 22429778-11 2012 Ocular irradiation from a Ru-106 plaque promoted an increase in the levels of IL-6, IL-8 and IL-1beta, modulation of which could be useful in managing radiation-related side effects. Ruthenium-106 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 22147632-7 2012 However, conditioned medium from CD4+ T cells cultured with tofacitinib inhibited IL-6 production by RASFs and IL-8 production by CD14+ monocytes. tofacitinib 60-71 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 22147632-8 2012 Treatment of SCID-HuRAg mice with tofacitinib decreased serum levels of human IL-6 and IL-8 and markedly suppressed invasion of synovial tissue into cartilage. tofacitinib 34-45 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 22147632-9 2012 CONCLUSION: Tofacitinib directly suppressed the production of IL-17 and IFNgamma and the proliferation of CD4+ T cells, resulting in inhibition of IL-6 production by RASFs and IL-8 production by CD14+ cells and decreased cartilage destruction. tofacitinib 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 22459196-4 2012 Together with results obtained using N-acetylcystein (NAC), we were able to clearly show that low level and early stage exposure to 5 nm silver nanoparticles, but not 100 nm, induces expression of IL-8 as well as stress genes against reactive oxygen species (ROS). Silver 137-143 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 22546346-0 2012 Dexamethasone reduces bilirubin-induced toxicity and IL-8 and MCP-1 release in human NT2-N neurons. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 22313893-0 2012 Regulation of the expression of interleukin-8 induced by 25-hydroxycholesterol in retinal pigment epithelium cells. 25-hydroxycholesterol 57-78 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 22313893-4 2012 PI3K-, MEK1/2-, ERK1/2- and NF-kappaB-specific inhibitors were used to assess the specific role of the several players on the regulation of IL-8 production by oxysterols. Oxysterols 159-169 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 22313893-7 2012 Indeed, treatment of ARPE-19 with 25-OH, but not with 7-KC, 7beta-OH or cholesterol, induced the secretion of IL-8 from cells. 25-oh 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 22281986-5 2012 Pre-exposure to FRH increased in vivo IL-8-directed PMN TAM by 23.5-fold and in vitro TEM by 7-fold. frh 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 22147632-5 2012 RESULTS: Tofacitinib treatment of CD4+ T cells originating from synovium and peripheral blood inhibited the production of interleukin-17 (IL-17) and interferon-gamma (IFNgamma) in a dose-dependent manner, affecting both proliferation and transcription, but had no effect on IL-6 and IL-8 production. tofacitinib 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 283-287 22326254-0 2012 Association of serum levels of polychlorinated biphenyls with IL-8 mRNA expression in blood samples from asthmatic and non-asthmatic Japanese children. Polychlorinated Biphenyls 31-56 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 22884152-9 2012 Parthenolide decreased the levels of the angiogenic factors MMP-9, VEGF, and IL-8 secreted by the MDA-MB-231 cells. parthenolide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 22313893-11 2012 Additionally, we also found that 25-OH decreases the levels of IkappaB and increases the nuclear levels of NF-kappaB p65 subunit and that inhibition of NF-kappaB activity partially prevents the increased secretion of IL-8 induced by 25-OH. 25-oh 233-238 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 22313893-12 2012 CONCLUSIONS: The results presented in this study suggest a role for 25-OH in inducing IL-8 production through pathways that are likely to involve AP-1 and NF-kappaB in ARPE-19 cells. 25-oh 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 22481026-8 2012 CFTR(inh172) also altered the release of inflammation mediators PGE(2) and IL-8, and this effect was blunted by exogenous 15d-PGJ(2). 15d-pgj 122-129 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 21932059-0 2012 ICAM-1 and IL-8 are expressed by DEHP and suppressed by curcumin through ERK and p38 MAPK in human umbilical vein endothelial cells. Curcumin 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 21932059-5 2012 Pretreatment with curcumin dose-dependently decreased DEHP-induced expression of ICAM-1 and IL-8 as well as phosphorylation of ERK1/2 and p38. Curcumin 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21932059-5 2012 Pretreatment with curcumin dose-dependently decreased DEHP-induced expression of ICAM-1 and IL-8 as well as phosphorylation of ERK1/2 and p38. Diethylhexyl Phthalate 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21932059-6 2012 Preincubation with ERK1/2 inhibitor (PD98059) or p38 inhibitor (SB203580) markedly blocked DEHP-stimulated activation of ICAM-1 and IL-8. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 21932059-6 2012 Preincubation with ERK1/2 inhibitor (PD98059) or p38 inhibitor (SB203580) markedly blocked DEHP-stimulated activation of ICAM-1 and IL-8. SB 203580 64-72 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 21932059-6 2012 Preincubation with ERK1/2 inhibitor (PD98059) or p38 inhibitor (SB203580) markedly blocked DEHP-stimulated activation of ICAM-1 and IL-8. Diethylhexyl Phthalate 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 21932059-7 2012 We suggest that curcumin inhibits DEHP-induced expression of ICAM-1 and IL-8 through ERK and p38 MAPK signaling pathways in HUVECs and may contribute to ameliorate pathologies of DEHP-related allergic disorders. Curcumin 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 21932059-7 2012 We suggest that curcumin inhibits DEHP-induced expression of ICAM-1 and IL-8 through ERK and p38 MAPK signaling pathways in HUVECs and may contribute to ameliorate pathologies of DEHP-related allergic disorders. Diethylhexyl Phthalate 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 21932059-7 2012 We suggest that curcumin inhibits DEHP-induced expression of ICAM-1 and IL-8 through ERK and p38 MAPK signaling pathways in HUVECs and may contribute to ameliorate pathologies of DEHP-related allergic disorders. Diethylhexyl Phthalate 179-183 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 21967620-0 2012 Evaluation of the tear and serum levels of IL-8 in sulfur mustard intoxicated patients 20 years after exposure. Mustard Gas 51-65 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 22768761-5 2012 RESULTS: The total amounts of IL-8 and GCF volume in the Ni-Cr alloy coated porcelain teeth were higher in different time period than those before treatment (P<0.05). ni-cr 57-62 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 22768761-9 2012 Therefore, the level of IL-8 in GCF is a useful criteria for the evaluation of stimulation degree on gingiva by different alloy coating materials in porcelain teeth. Alloys 122-127 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 22498762-12 2012 Curcumin also inhibited the TNF-alpha-induced production of IL-6/IL-8 in HaCaT cells. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 22324515-9 2012 Interleukin-8 and vascular endothelial growth factor transcripts were induced after neuropeptides treatment, but downregulated by bortezomib. Bortezomib 130-140 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 22556343-4 2012 Assessing the regulatory function of miR-93/106b through doxycycline-inducible lentiviral transduction in a microarray analysis, tissue factor (F3) and IL8 were identified as their possible targets. Doxycycline 57-68 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 21938724-0 2012 Imatinib treatment inhibit IL-6, IL-8, NF-KB and AP-1 production and modulate intracellular calcium in CML patients. Imatinib Mesylate 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 21938724-7 2012 Our results demonstrated a significant down-regulation in IL-6 and IL-8 release as well as NF-kB and AP-1 activation in lymphomonocytes from Imatinib-treated patients, compared to samples from untreated patients. Imatinib Mesylate 141-149 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 21938724-9 2012 The results of this study show that measurements of NF-kB, AP-1, IL-6, IL-8, and intracellular calcium in CML patients treated with Imatinib may give important information to the hematologist on diagnostic criteria and are highly predictive in patients with newly diagnosed CML. Imatinib Mesylate 132-140 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 22009527-0 2012 Enhancement of interleukin-8-induced chemotactic response and reactive oxygen species production in HL-60 cells expressing CXCR1. Reactive Oxygen Species 62-85 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 22009527-5 2012 When these cell lines were primed with CXC chemokine ligand 8 (IL-8), a slight increase in reactive oxygen species production induced by phorbol myristate acetate (PMA) or zymosan A stimuli was observed. Reactive Oxygen Species 91-114 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 22009527-5 2012 When these cell lines were primed with CXC chemokine ligand 8 (IL-8), a slight increase in reactive oxygen species production induced by phorbol myristate acetate (PMA) or zymosan A stimuli was observed. Tetradecanoylphorbol Acetate 137-162 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 22009527-5 2012 When these cell lines were primed with CXC chemokine ligand 8 (IL-8), a slight increase in reactive oxygen species production induced by phorbol myristate acetate (PMA) or zymosan A stimuli was observed. Tetradecanoylphorbol Acetate 164-167 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 22009527-5 2012 When these cell lines were primed with CXC chemokine ligand 8 (IL-8), a slight increase in reactive oxygen species production induced by phorbol myristate acetate (PMA) or zymosan A stimuli was observed. Zymosan 172-181 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 21840193-9 2012 These results suggest that linoleic acid-induced changes in monocyte chemotaxis and subsequent binding are not solely mediated by changes in adhesion molecule expression but may be due to secreted factors such as IL-8, monocyte chemoattractant protein-1 or prostaglandins (PGs) such as PGE(2), as IL-8 neutralisation and COX-2 inhibition reduced monocyte binding without changes in adhesion molecule expression. Linoleic Acid 27-40 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 21840193-9 2012 These results suggest that linoleic acid-induced changes in monocyte chemotaxis and subsequent binding are not solely mediated by changes in adhesion molecule expression but may be due to secreted factors such as IL-8, monocyte chemoattractant protein-1 or prostaglandins (PGs) such as PGE(2), as IL-8 neutralisation and COX-2 inhibition reduced monocyte binding without changes in adhesion molecule expression. Linoleic Acid 27-40 C-X-C motif chemokine ligand 8 Homo sapiens 297-301 22571267-7 2012 TFB intervention may significantly suppressed the supernatant IL-8, TNF-alpha and NO levels of HUVEC. tfb 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 22421092-3 2012 This study aimed to compare the surface rehardening and fluoride uptake effect of 2%-NaF solutions at different pH on non-cavitated caries-like lesions with two different levels of demineralization. Fluorides 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 22464230-6 2012 RESULTS: Kojic acid increased interleukin (IL)-6 and IL-8 production in melanocyte/keratinocyte co-cultures; however, IL-6 directly inhibited melanogenesis whereas IL-8 did not. kojic acid 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 22464230-6 2012 RESULTS: Kojic acid increased interleukin (IL)-6 and IL-8 production in melanocyte/keratinocyte co-cultures; however, IL-6 directly inhibited melanogenesis whereas IL-8 did not. kojic acid 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 22768425-5 2012 After 24h of treatment, IL-8 protein release from A549 cells, induced by 10, 50 and 250 microg/ml of P25 TiO2 NPs, were statistically significantly raised, compared to that of the control. titanium dioxide 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 22768425-6 2012 This finding corroborates existing literature in that TiO2 NPs induce a dose-dependent increase in the release of IL-8 protein when exposed to A549 cells. titanium dioxide 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 22401993-3 2012 Corticosteroid sensitivity was determined as IC50 to dexamethasone (Dex) on TNFalpha-induced IL-8 release in a U937 monocytic cell line (Dex-IC50). Dexamethasone 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 22401993-3 2012 Corticosteroid sensitivity was determined as IC50 to dexamethasone (Dex) on TNFalpha-induced IL-8 release in a U937 monocytic cell line (Dex-IC50). Dexamethasone 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 22932481-1 2012 OBJECTIVE: To investigate the effects of 17-beta estradiol (E(2)) and Porphyromonas gingivalis (Pg) W83 on the expression of interleukin (IL)-6 and IL-8 in human periodontal ligament cells (hPDLC). Estradiol 41-58 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 22574737-10 2012 RESULTS: Compared with placebo, butyrate therapy led to the early reduction of macrophages, pus cells, IL-8 and IL-1beta in the stool and improvement in rectal histopathology. Butyrates 32-40 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 22387535-2 2012 In this study I found that biochanin, a methoxy form of genistein, inhibits IL-8-mediated activation of nuclear transcription factor kappaB (NF-kappaB) and activator protein 1 (AP-1) more potently than genistein as shown in Jurkat T-cell line. Genistein 56-65 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 22387535-2 2012 In this study I found that biochanin, a methoxy form of genistein, inhibits IL-8-mediated activation of nuclear transcription factor kappaB (NF-kappaB) and activator protein 1 (AP-1) more potently than genistein as shown in Jurkat T-cell line. Genistein 202-211 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 22181939-4 2012 TLRs expression was examined by RT-PCR and IL-8 production by poly I:C was examined by ELISA. poly I:C 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 21344174-8 2012 Theanine also repressed phorbol 12-myristate 13-acetate and calcium ionophore A23187-induced TNF-alpha, IL-1beta, IL-6, and IL-8 secretion by suppressing NF-kappaB activation. theanine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 22059850-6 2012 RESULTS: Short-chain fatty acids, at 20 mM, induced interleukin (IL)-8, IL-6, and IL-1beta release, while lower levels (0.02-2 mM) did not induce cytokine secretion. Fatty Acids, Volatile 9-32 C-X-C motif chemokine ligand 8 Homo sapiens 52-70 21344174-8 2012 Theanine also repressed phorbol 12-myristate 13-acetate and calcium ionophore A23187-induced TNF-alpha, IL-1beta, IL-6, and IL-8 secretion by suppressing NF-kappaB activation. Calcimycin 78-84 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 22465753-0 2012 Lysophosphatidic acid induces lymphangiogenesis and IL-8 production in vitro in human lymphatic endothelial cells. lysophosphatidic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 22465753-5 2012 In addition, LPA induces IL-8 expression by enhancing IL-8 promoter activity via activation of the NF-kappaB pathway in LECs. lysophosphatidic acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 22465753-5 2012 In addition, LPA induces IL-8 expression by enhancing IL-8 promoter activity via activation of the NF-kappaB pathway in LECs. lysophosphatidic acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 22465753-6 2012 Using IL-8 siRNA and IL-8 neutralizing antibody, we revealed that IL-8 plays an important role in LPA-induced lymphangiogenesis in vitro. lysophosphatidic acid 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 22465753-6 2012 Using IL-8 siRNA and IL-8 neutralizing antibody, we revealed that IL-8 plays an important role in LPA-induced lymphangiogenesis in vitro. lysophosphatidic acid 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 22465753-6 2012 Using IL-8 siRNA and IL-8 neutralizing antibody, we revealed that IL-8 plays an important role in LPA-induced lymphangiogenesis in vitro. lysophosphatidic acid 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 22465753-7 2012 Moreover, using siRNA inhibition, we discovered that LPA-induced lymphangiogenesis in vitro and IL-8 production are mediated via the LPA(2) receptor in LECs. lysophosphatidic acid 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 22465753-8 2012 Finally, using human sentinel afferent lymphatic vessel explants, we demonstrated that LPA up-regulates IL-8 production in the LECs of lymphatic endothelia. lysophosphatidic acid 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 22465753-9 2012 These studies provide the first evidence that LPA promotes lymphangiogenesis and induces IL-8 production in LECs; we also reveal a possible new role of LPA in the promotion of tumor progression, as well as metastasis, in different cancer types. lysophosphatidic acid 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 22402363-3 2012 The oxidation products of phospholipids, including oxidized 1-palmitoyl-2-arachidonyl-sn-glycerol-3-phosphocholine (Ox-PAPC), accumulate in atherosclerotic lesions and strongly induce IL-8 in human aortic endothelial cells (HAECs). Phospholipids 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 22271211-2 2012 In this study, data collected on RHE exposed to well-characterized sensitizing chemicals, such as dinitrofluorobenzene, oxazolone, cinnamaldehyde and isoeugenol, revealed a transient expression of IL-8 mRNA in association with abundant IL-8 cell release. Dinitrofluorobenzene 98-118 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 22271211-2 2012 In this study, data collected on RHE exposed to well-characterized sensitizing chemicals, such as dinitrofluorobenzene, oxazolone, cinnamaldehyde and isoeugenol, revealed a transient expression of IL-8 mRNA in association with abundant IL-8 cell release. Dinitrofluorobenzene 98-118 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 22271211-2 2012 In this study, data collected on RHE exposed to well-characterized sensitizing chemicals, such as dinitrofluorobenzene, oxazolone, cinnamaldehyde and isoeugenol, revealed a transient expression of IL-8 mRNA in association with abundant IL-8 cell release. Oxazolone 120-129 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 22402363-3 2012 The oxidation products of phospholipids, including oxidized 1-palmitoyl-2-arachidonyl-sn-glycerol-3-phosphocholine (Ox-PAPC), accumulate in atherosclerotic lesions and strongly induce IL-8 in human aortic endothelial cells (HAECs). 1-palmitoyl-2-arachidonyl-sn-glycerol-3-phosphocholine 60-114 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 22271211-2 2012 In this study, data collected on RHE exposed to well-characterized sensitizing chemicals, such as dinitrofluorobenzene, oxazolone, cinnamaldehyde and isoeugenol, revealed a transient expression of IL-8 mRNA in association with abundant IL-8 cell release. Oxazolone 120-129 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 22271211-2 2012 In this study, data collected on RHE exposed to well-characterized sensitizing chemicals, such as dinitrofluorobenzene, oxazolone, cinnamaldehyde and isoeugenol, revealed a transient expression of IL-8 mRNA in association with abundant IL-8 cell release. cinnamaldehyde 131-145 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 22271211-2 2012 In this study, data collected on RHE exposed to well-characterized sensitizing chemicals, such as dinitrofluorobenzene, oxazolone, cinnamaldehyde and isoeugenol, revealed a transient expression of IL-8 mRNA in association with abundant IL-8 cell release. isoeugenol 150-160 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 22271211-2 2012 In this study, data collected on RHE exposed to well-characterized sensitizing chemicals, such as dinitrofluorobenzene, oxazolone, cinnamaldehyde and isoeugenol, revealed a transient expression of IL-8 mRNA in association with abundant IL-8 cell release. isoeugenol 150-160 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 22402363-11 2012 Free thiol cysteine analogs showed inhibition of IL-8 induction by Ox-PAPC, and both a cysteine analog and a cell surface thiol blocker strongly inhibited ADAM activity induction by Ox-PAPC. thiol-cysteine 5-19 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 22402363-11 2012 Free thiol cysteine analogs showed inhibition of IL-8 induction by Ox-PAPC, and both a cysteine analog and a cell surface thiol blocker strongly inhibited ADAM activity induction by Ox-PAPC. Cysteine 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 22402363-11 2012 Free thiol cysteine analogs showed inhibition of IL-8 induction by Ox-PAPC, and both a cysteine analog and a cell surface thiol blocker strongly inhibited ADAM activity induction by Ox-PAPC. Sulfhydryl Compounds 5-10 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 22285804-9 2012 We demonstrate that the synthetic glucocorticoid dexamethasone (Dex) significantly decreases IL-8 secretion, AP-1 and NF-kappaB activity in CF cells in a pro-inflammatory context. Dexamethasone 49-62 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 22465636-2 2012 The introduction of A ring pyrazole modification to the hydrocortisone C-21 heteroaryl thioethers generated compounds with excellent transrepression potency (IL-8 inhibition) compared to their hydrocortisone analogs. pyrazole 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 22465636-2 2012 The introduction of A ring pyrazole modification to the hydrocortisone C-21 heteroaryl thioethers generated compounds with excellent transrepression potency (IL-8 inhibition) compared to their hydrocortisone analogs. Hydrocortisone 56-70 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 22465636-2 2012 The introduction of A ring pyrazole modification to the hydrocortisone C-21 heteroaryl thioethers generated compounds with excellent transrepression potency (IL-8 inhibition) compared to their hydrocortisone analogs. Sulfides 87-97 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 22436383-7 2012 Dithiolethione-mediated inhibition of NF-kappaB-regulated genes resulted in the inhibition of interleukin (IL)-6, IL-8, urokinase-type plasminogen activator, and VEGF production. dithiolethione 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 22726350-3 2012 ST, rosmarinic acid, pulegone, and 2alpha,3alpha,24-thrihydrooxylen-12en-28oic acid treatment of HMC-1 cells led to significant suppression of pro-inflammatory cytokines (IL-6, IL-8, and TNF-alpha) in a dose dependent manner. rosmarinic acid 4-19 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 22726350-3 2012 ST, rosmarinic acid, pulegone, and 2alpha,3alpha,24-thrihydrooxylen-12en-28oic acid treatment of HMC-1 cells led to significant suppression of pro-inflammatory cytokines (IL-6, IL-8, and TNF-alpha) in a dose dependent manner. pulegone 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 22726350-3 2012 ST, rosmarinic acid, pulegone, and 2alpha,3alpha,24-thrihydrooxylen-12en-28oic acid treatment of HMC-1 cells led to significant suppression of pro-inflammatory cytokines (IL-6, IL-8, and TNF-alpha) in a dose dependent manner. 24-thrihydrooxylen-12en-28oic acid 49-83 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 22119045-0 2012 Nicotine up-regulates IL-8 expression in human gingival epithelial cells following stimulation with IL-1beta or P. gingivalis lipopolysaccharide via nicotinic acetylcholine receptor signalling. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 22119045-2 2012 The aim of this study is to evaluate the effect of nicotine, a major component of cigarette smoke, on interleukin-8 (IL-8) production and cellular signalling via nicotinic acetylcholine receptors (nAChRs) in human gingival epithelial cells (HGECs). Nicotine 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 22119045-2 2012 The aim of this study is to evaluate the effect of nicotine, a major component of cigarette smoke, on interleukin-8 (IL-8) production and cellular signalling via nicotinic acetylcholine receptors (nAChRs) in human gingival epithelial cells (HGECs). Nicotine 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 22119045-8 2012 Nicotine increased the secretion of IL-8 from HGECs that were cultured in the presence of IL-1beta or P. gingivalis LPS and also induced the phosphorylation of extracellular signal-regulated kinase (ERK) in epi 4. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 22119045-10 2012 Furthermore, nicotine-induced IL-8 secretion was decreased by pretreatment with non-selective nAChR antagonist, ERK1/2 inhibitor or intracellular calcium chelator. Nicotine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 22119045-10 2012 Furthermore, nicotine-induced IL-8 secretion was decreased by pretreatment with non-selective nAChR antagonist, ERK1/2 inhibitor or intracellular calcium chelator. Calcium 146-153 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 22119045-11 2012 CONCLUSION: These findings indicate that nicotine increases IL-8 production in gingival epithelial cells via ERK phosphorylation following Ca(2+) signalling after nAChR activation. Nicotine 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 22471285-5 2012 Interleukin (IL)-6 and IL-8 mRNA expression and protein secretion in LPS-stimulated cells were inhibited significantly by the lipophilic statin pitavastatin and the hydrophilic statin pravastatin. pitavastatin 144-156 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 22471285-5 2012 Interleukin (IL)-6 and IL-8 mRNA expression and protein secretion in LPS-stimulated cells were inhibited significantly by the lipophilic statin pitavastatin and the hydrophilic statin pravastatin. Pravastatin 184-195 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 22475920-0 2012 Atlas of sodium fluoride PET bone scans: atlas of NaF PET bone scans. Sodium Fluoride 9-24 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 22475920-1 2012 Sodium fluoride (NaF) is a bone-seeking positron-emitting tracer with high sensitivity and specificity for detection of osseous lesions, particularly osteolytic lesions. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 22367719-3 2012 In vitro, endotoxin-mediated induction of endothelial permeability and IL-8-induced transmigration of neutrophils through human microvascular endothelial cells required ADAM17 as shown by inhibition with GW280264X or shRNA-mediated knockdown. GW280264X 204-213 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 22285804-9 2012 We demonstrate that the synthetic glucocorticoid dexamethasone (Dex) significantly decreases IL-8 secretion, AP-1 and NF-kappaB activity in CF cells in a pro-inflammatory context. Dexamethasone 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 22285804-10 2012 Moreover, we show that p38 MAPK controls IL-8 release by determining GR activation through specific phosphorylation on serine 211. Serine 119-125 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 22285804-11 2012 Finally, we demonstrate a synergistic effect of dexamethasone treatment and inhibition of p38 MAPK inducing more than 90% inhibition of IL-8 production in CF cells. Dexamethasone 48-61 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 22415150-0 2012 Elevated tear interleukin-6 and interleukin-8 levels associated with silicone hydrogel and conventional hydrogel contact lens wear. Silicones 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 22415150-11 2012 CONCLUSIONS: The SH-CL and CH-CL wear is associated with elevation of IL-6 and IL-8 levels in the tears of healthy, nonatopic neophyte CL users. ch-cl 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 22399514-12 2012 TSH induces IL-8 production at the pretranslational level. Thyrotropin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 22267101-8 2012 Additionally, the levels of IL-6 and IL-8 mRNA induced by TNF-alpha were significantly suppressed by the addition of cinobufocini. cinobufocini 141-153 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 22648625-9 2012 Uro-A inhibited endothelial cell migration and was able to decrease the expression of CCL2 and interleukin-8 (IL-8). 3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 22648625-9 2012 Uro-A inhibited endothelial cell migration and was able to decrease the expression of CCL2 and interleukin-8 (IL-8). 3,8-dihydroxy-6H-dibenzo(b,d)pyran-6-one 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 22399514-11 2012 These cells produce high levels of several cytokines and chemokines including IL-8, regulated upon activation, normal T cell expressed and secreted, and monocyte chemoattractant protein-1 when treated with TSH or M22. Thyrotropin 206-209 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 21984511-5 2012 JPT and HES inhibited the H(2)O(2)-induced interleukin-8 and tumor necrosis factor-alpha production as well as its mRNA expression. JPT 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 43-88 22045098-12 2012 The effluent concentration of interleukin 8 was significantly lower in patients using low-GDP PDF. Guanosine Diphosphate 90-93 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 22215656-11 2012 In comparing the BicaVera and standard solution groups, MCs from the standard solution group showed significantly higher secretion of interleukin 8 and lower secretion of collagen I, but no differences in the levels of other EMT-associated molecules, including fibronectin, VEGF, E-cadherin, and transforming growth factor beta1. mcs 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 134-147 22215656-14 2012 CONCLUSIONS: Effluent MCs grown ex vivo from patients treated with bicarbonate/low-GDP BicaVera fluid showed a trend to acquire an epithelial phenotype, with lower production of proinflammatory cytokines and chemokines (such as interleukin 8) than was seen with MCs from patients treated with a lactate-buffered standard PD solution. mcs 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 228-241 22215656-14 2012 CONCLUSIONS: Effluent MCs grown ex vivo from patients treated with bicarbonate/low-GDP BicaVera fluid showed a trend to acquire an epithelial phenotype, with lower production of proinflammatory cytokines and chemokines (such as interleukin 8) than was seen with MCs from patients treated with a lactate-buffered standard PD solution. Bicarbonates 67-78 C-X-C motif chemokine ligand 8 Homo sapiens 228-241 21984511-5 2012 JPT and HES inhibited the H(2)O(2)-induced interleukin-8 and tumor necrosis factor-alpha production as well as its mRNA expression. Hesperidin 8-11 C-X-C motif chemokine ligand 8 Homo sapiens 43-88 21984511-5 2012 JPT and HES inhibited the H(2)O(2)-induced interleukin-8 and tumor necrosis factor-alpha production as well as its mRNA expression. Hydrogen Peroxide 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 43-88 22356551-1 2012 Sodium fluoride (NaF) has been shown to be cytotoxic and produces inflammatory responses in humans. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 22763297-6 2012 Serum levels of IL-8 and IL-12p40 on admission were higher in patients with SAAP than in patients with MAAP but the difference was not statistically significant. saap 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 22763297-6 2012 Serum levels of IL-8 and IL-12p40 on admission were higher in patients with SAAP than in patients with MAAP but the difference was not statistically significant. maap 103-107 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 22403260-4 2012 CD161(+)CD56(+)LFA-1(-) NK cells produce large amounts of CXCL8 after phorbol myristate acetate (PMA) or cytokine treatment. Tetradecanoylphorbol Acetate 70-95 C-X-C motif chemokine ligand 8 Homo sapiens 58-63 22477013-0 2012 Phagocytosis and endocytosis of silver nanoparticles induce interleukin-8 production in human macrophages. Silver 32-38 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 22427570-7 2012 Both melphalan and carboplatin triggered human retinal endothelial cell migration, proliferation, apoptosis, and increased expression of adhesion proteins intracellullar adhesion molecule-1 [ICAM-1] and soluble chemotactic factors (IL-8). Melphalan 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 22427570-7 2012 Both melphalan and carboplatin triggered human retinal endothelial cell migration, proliferation, apoptosis, and increased expression of adhesion proteins intracellullar adhesion molecule-1 [ICAM-1] and soluble chemotactic factors (IL-8). Carboplatin 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 22403260-4 2012 CD161(+)CD56(+)LFA-1(-) NK cells produce large amounts of CXCL8 after phorbol myristate acetate (PMA) or cytokine treatment. Tetradecanoylphorbol Acetate 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 58-63 22416137-6 2012 Pretreatment of NCM460 cells with the ECE-1 inhibitor SM19712 or gene silencing of betaARR1 or betaARR2 inhibits NT-stimulated ERK1/2 and JNK phosphorylation, NF-kappaB p65 nuclear translocation and phosphorylation, and IL-8 secretion. SM 19712 54-61 C-X-C motif chemokine ligand 8 Homo sapiens 220-224 22490085-7 2012 With sitosterol, campesterol, and 7-ketositosterol, IL-8 secretion was decreased, and with campesterol the intracellular polar lipid level was reduced. gamma-sitosterol 5-15 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 22490085-7 2012 With sitosterol, campesterol, and 7-ketositosterol, IL-8 secretion was decreased, and with campesterol the intracellular polar lipid level was reduced. campesterol 17-28 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 22490085-7 2012 With sitosterol, campesterol, and 7-ketositosterol, IL-8 secretion was decreased, and with campesterol the intracellular polar lipid level was reduced. 7-ketositosterol 34-50 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 22323305-14 2012 The LCI correlated with bronchoalveolar lavage IL-8 (R(2) = 0.20, P = 0.004) and neutrophil count (R(2) = 0.21, P = 0.001). Casein Kinase inhibitor A86 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 22095388-9 2012 Cells pretreated with nicotine prior to lipopolysaccharide (LPS) stimulation exhibited a lower production of TNF-alpha, IL-8, and IL-6 compared to LPS-treated (only) cells. Nicotine 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 22322153-7 2012 PFOA induced gene expression of pro-inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, IL-6, and IL-8 in mast cells. perfluorooctanoic acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 22469443-6 2012 RESULTS: Serum levels of IL-8, MCP-1, and CCL-20 were significantly higher in the AS group than in the AR and NA groups. Arsenic 82-84 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 22460142-7 2012 Tofacitinib reduced serum levels of human IL-6 and IL-8 in the mice and also reduced synovial inflammation and invasion into the implanted cartilage. tofacitinib 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 22274300-0 2012 Modulatory effect of fenofibrate on endothelial production of neutrophil chemokines IL-8 and ENA-78. Fenofibrate 21-32 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 22473315-0 2012 Lactate-induced IL-8 pathway in endothelial cells--letter. Lactic Acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 22095388-10 2012 Cells that were transfected with alpha7 siRNA and subsequently incubated with nicotine and LPS, exhibited a higher expression of TNF-alpha, IL-8, and IL-6 compared with non-transfected cells or alpha1 and alpha5 siRNA-transfected cells. Nicotine 78-86 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 22531917-0 2012 Prostaglandin E2 modulates IL-8 expression through formation of a multiprotein enhanceosome in human colonic epithelial cells. Dinoprostone 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 22484638-11 2012 In vivo, IL-8 expression was non-significantly suppressed in the curcumin-supplemented patients compared to the squamous control tissue, whilst also showing a doubling in the apoptotic frequency compared to non-supplemented control patients. Curcumin 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 22457139-0 2012 Effect of puerarin on the release of interleukin-8 in co-culture of human bronchial epithelial cells and neutrophils. puerarin 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 22457139-7 2012 Treatment with puerarin could significantly down-regulate the expression of IL-8 mRNA in BEAS-2B cells and IL-8 release in the supernatant of the co-culture of BEAS-2B cells and neutrophils (P<0.01). puerarin 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 22457139-7 2012 Treatment with puerarin could significantly down-regulate the expression of IL-8 mRNA in BEAS-2B cells and IL-8 release in the supernatant of the co-culture of BEAS-2B cells and neutrophils (P<0.01). puerarin 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 22457139-8 2012 CONCLUSION: Puerarin could exhibit anti-inflammatory activity by suppressing IL-8 production from the co-culture of human bronchial epithelial cells and neutrophils. puerarin 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 22045303-3 2012 The aim of this study was to evaluate the effects of one of the most widespread mycotoxin, ochratoxin A (OTA), on the release of pro-inflammatory cytokines such as interleukin-(IL)-6 and the CXC-chemokine IL-8 from nasal epithelial cell cultures (NEC) of subjects with and without ECRS. ochratoxin A 91-103 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 22531917-2 2012 PGE(2) binding and coupling through EP2/4 receptor subtypes on colonic epithelial cells stimulates cyclic adenosine monophosphate (cAMP) and IL-8 production. Dinoprostone 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 22531917-3 2012 Here we determined the mechanisms whereby PGE(2) regu-lates IL-8 in Caco2 colonic epithelial cells and in cells over-expressing the EP2/4 receptors (EP2S/EP4S). Prostaglandins E 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 22531917-7 2012 PGE(2) coupling through EP2/4 receptors can therefore acts in an opposing manner to either decrease (EP2) or promote IL-8 expression by recruiting CREB-binding protein (CBP) (EP4), which formed a multiprotein IL-8 enhanceosome. Prostaglandins E 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 22531917-7 2012 PGE(2) coupling through EP2/4 receptors can therefore acts in an opposing manner to either decrease (EP2) or promote IL-8 expression by recruiting CREB-binding protein (CBP) (EP4), which formed a multiprotein IL-8 enhanceosome. Prostaglandins E 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 22531917-9 2012 These data unravel the mechanisms by which expression of IL-8 is controlled by different signalling pathways that are activated by PGE(2) but acting through different EP receptors. Dinoprostone 131-137 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 22366056-3 2012 Results showed that testosterone at pharmacological doses reduced the production of interleukin-8 and reactive oxygen species from differentiated HL-60 cells in a concentration dependent manner without affecting phagocytosis. Testosterone 20-32 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 22105228-4 2012 (1) In human HCC cell lines (HCC-1.2, HCC-3, and SNU398) linoleic acid peroxide (LOOH) and other prooxidants enhanced the expression of VEGF and IL-8. snu398 49-55 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 22105228-4 2012 (1) In human HCC cell lines (HCC-1.2, HCC-3, and SNU398) linoleic acid peroxide (LOOH) and other prooxidants enhanced the expression of VEGF and IL-8. linoleic acid peroxide 57-79 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 22105228-4 2012 (1) In human HCC cell lines (HCC-1.2, HCC-3, and SNU398) linoleic acid peroxide (LOOH) and other prooxidants enhanced the expression of VEGF and IL-8. Lipid Peroxides 81-85 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 22105228-13 2012 In contrast, selenium inversely correlated with VEGF, IL-8, and HCC size (the latter only for tumors smaller than 3 cm). Selenium 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 22068339-6 2012 Se depletion decreased expression of glutathione peroxidase1 (GPX1) and selenoproteins H and W and increased TNFalpha-stimulated luciferase activity, endogenous IL-8 expression and reactive oxygen species (ROS) production. Selenium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 22487368-5 2012 Quercetin, one of the active components in Calendula, has been shown to inhibit recombinant human matrix metalloproteinase (MMP) activity and decrease the expression of tumor necrosis factor-alpha, interleukin-1beta (IL), IL-6 and IL-8 in phorbol 12-myristate 13-acetate and calcium ionophore-stimulated human mast cells. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 231-235 22366056-5 2012 At the highest concentration of testosterone (120 muM), interleukin-8 secretion was reduced 42-80%, and production of reactive oxygen species was reduced 32-46%. Testosterone 32-44 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 22366056-9 2012 Testosterone, at pharmacological doses, was also shown to suppress generation of reactive oxygen species and interleukin-8 in human granulocytes and monocytes, respectively, to a similar extent as observed in differentiated HL-60 cells. Testosterone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 109-122 21479710-2 2012 (18)F sodium fluoride ((18)F NaF) positron emission tomography (PET)/computed tomography (CT) has better resolution and is considered superior. Sodium Fluoride 6-21 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 22218461-9 2012 Tri-DAP and MDP led to the production of IL-6 and IL-8 and the activation of NF-kappaB and MAPK in PDL cells. Acetylmuramyl-Alanyl-Isoglutamine 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 22357660-0 2012 Ribavirin regulates hepatitis C virus replication through enhancing interferon-stimulated genes and interleukin 8. Ribavirin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 22357660-7 2012 RBV upregulated interleukin 8 (IL-8) in the absence of IFN-alpha. Ribavirin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 22357660-7 2012 RBV upregulated interleukin 8 (IL-8) in the absence of IFN-alpha. Ribavirin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 22357660-8 2012 The IL-8 upregulation induced by RBV was responsible for the activation of activator protein 1 (AP-1). Ribavirin 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 22357660-10 2012 Moreover, RBV can enhance IL-8 through activating AP-1. Ribavirin 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 21951103-0 2012 Melatonin suppresses acrolein-induced IL-8 production in human pulmonary fibroblasts. Melatonin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 21951103-0 2012 Melatonin suppresses acrolein-induced IL-8 production in human pulmonary fibroblasts. Acrolein 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 21951103-3 2012 Furthermore, recent studies show that, alpha, beta-unsaturated aldehyde acrolein in CS induces the production of interleukin (IL)-8, which is known to be related to bronchitis, rhinitis, pulmonary fibrosis, and asthma. alpha, beta-unsaturated aldehyde acrolein 39-80 C-X-C motif chemokine ligand 8 Homo sapiens 113-131 21951103-3 2012 Furthermore, recent studies show that, alpha, beta-unsaturated aldehyde acrolein in CS induces the production of interleukin (IL)-8, which is known to be related to bronchitis, rhinitis, pulmonary fibrosis, and asthma. Cesium 84-86 C-X-C motif chemokine ligand 8 Homo sapiens 113-131 21951103-6 2012 In this study, we investigated whether melatonin suppresses acrolein-induced IL-8 secretion in human pulmonary fibroblasts (HPFs). Melatonin 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 21951103-6 2012 In this study, we investigated whether melatonin suppresses acrolein-induced IL-8 secretion in human pulmonary fibroblasts (HPFs). Acrolein 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 21951103-7 2012 It was found that acrolein-induced IL-8 production was accompanied by increased levels of phosphorylation of Akt and extracellular signal-regulated kinases (ERK1/2) in HPFs, and that melatonin suppressed IL-8 production in HPFs. Acrolein 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 21951103-7 2012 It was found that acrolein-induced IL-8 production was accompanied by increased levels of phosphorylation of Akt and extracellular signal-regulated kinases (ERK1/2) in HPFs, and that melatonin suppressed IL-8 production in HPFs. Acrolein 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 21951103-7 2012 It was found that acrolein-induced IL-8 production was accompanied by increased levels of phosphorylation of Akt and extracellular signal-regulated kinases (ERK1/2) in HPFs, and that melatonin suppressed IL-8 production in HPFs. Melatonin 183-192 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 21951103-8 2012 These results suggest that melatonin suppresses acrolein-induced IL-8 production via ERK1/2 and phosphatidylinositol 3-kinase (PI3K)/Akt signal inhibition in HPFs. Melatonin 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 21951103-8 2012 These results suggest that melatonin suppresses acrolein-induced IL-8 production via ERK1/2 and phosphatidylinositol 3-kinase (PI3K)/Akt signal inhibition in HPFs. Acrolein 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 22697068-4 2012 Indeed, differentiated THP-1 cell exposures (i) to 5 and 10 microM of combination of NP and DiP induced an IL-8 level in the medium respectively of 28.9 and 45 percent higher than the level obtained for the control (untreated cells), (ii) to combination of NP and DiP at 10 microM induced an increase of IL-1beta level in comparison to the control level, (iii) to combination of NP and DiP induced an increase of TNF-alpha level whatever the concentration of EDCs tested (between 0 and 10 microM). diisononyl phthalate 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 22093110-5 2012 Pre-incubating HUVECs with NAC prevented the effects induced by 5.0 mM of NaF and 0.5 mM of Sn(2) F. Acetylcysteine 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 22310660-4 2012 Consequently, induction of cytokines interleukin-8 and beta interferon after poly(I C) stimulation was impaired in Rb(-/-) MEF and Rb siRNA-transfected cells compared to controls. Poly I-C 77-88 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 21633399-8 2012 The oral glucose challenge was associated with a significant increase in the expression of inflammatory cytokines, including interleukin (IL)-1alpha/beta, IL-6, and IL-8, that may result from ER stress. Glucose 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 22392142-0 2012 NADPH oxidase-derived superoxide destabilizes lipopolysaccharide-induced interleukin 8 mRNA via p38, extracellular signal-regulated kinase mitogen-activated protein kinase, and the destabilizing factor tristetraprolin. Superoxides 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 21748755-0 2012 Lenalidomide modulates IL-8 and anti-prostate antibody levels in men with biochemically recurrent prostate cancer. Lenalidomide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 22408359-5 2012 RESULTS: The overexpression of IL-8 resulted in an increased cell adhesion, migration and invasion, and a significant resistance to oxaliplatin in MKN-45 cells. Oxaliplatin 132-143 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 22452847-3 2012 Recently, we reported that the protein kinase A (PKA) inhibitor H-89 suppresses lipopolysaccharide (LPS)-induced IL-8 production by human gingival fibroblasts (HGFs). N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 22452847-4 2012 In the present study, the relevance of the PKA activity and two PKA-activating drugs, aminophylline and adrenaline, to LPS-induced inflammatory cytokines (IL-6 and IL-8) and PGE2 by HGFs were examined. Aminophylline 86-99 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 22452847-4 2012 In the present study, the relevance of the PKA activity and two PKA-activating drugs, aminophylline and adrenaline, to LPS-induced inflammatory cytokines (IL-6 and IL-8) and PGE2 by HGFs were examined. Epinephrine 104-114 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 22452847-8 2012 In contrast, dbcAMP significantly increased LPS-induced IL-6, IL-8, and PGE2 production. Bucladesine 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 22227206-8 2012 HPAH PASMCs exhibited enhanced IL-6 and IL-8 induction by TGF-beta1, an effect reversed by NF-kappaB inhibition. pasmcs 5-11 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 22227206-9 2012 Moreover, neutralizing antibodies to IL-6 or IL-8 restored the antiproliferative effect of TGF-beta1 in HPAH PASMCs. pasmcs 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 22420994-0 2012 Involvement of metabotropic glutamate receptor 5, AKT/PI3K signaling and NF-kappaB pathway in methamphetamine-mediated increase in IL-6 and IL-8 expression in astrocytes. Methamphetamine 94-109 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 22420994-10 2012 Also, LY294002, an inhibitor of the Akt/PI3K pathway, abrogated the MA-mediated induction of IL-6 and IL-8 by 77.9 +- 6.6% and 81.4 +- 2.6%, respectively. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 22228760-8 2012 Pretreatment with a chemical chaperone, phenylbutyric acid, or adenoviral transfection with ATF6 attenuated HNE-induced monocyte adhesion and IL-8 induction. 4-phenylbutyric acid 40-58 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 22356100-6 2012 Caffeic acid at <=20 muM demoted resistin-stimulated interleukin 8 (IL-8) production responsible for ICAM-1 and beta2 integrin induction. caffeic acid 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 22356100-6 2012 Caffeic acid at <=20 muM demoted resistin-stimulated interleukin 8 (IL-8) production responsible for ICAM-1 and beta2 integrin induction. caffeic acid 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 22356100-7 2012 The endothelial up-regulation of IL-8 secretion by resistin entailed toll-like receptor 4 (TLR4) activation, but caffeic acid diminished IL-8 production and TLR4 induction. caffeic acid 113-125 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 22356100-9 2012 These results demonstrate that caffeic acid blocked monocyte trafficking to resistin-activated endothelium via disturbing NF-kappaB signaling responsive to IL-8. caffeic acid 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 22408359-6 2012 Inhibition of IL-8 expression with small interfering RNA decreased the adhesion, migration and invasion functions and oxaliplatin resistance in KATO-III cells. Oxaliplatin 118-129 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 22410118-0 2012 1,3-Diphenylpropenone ameliorates TNBS-induced rat colitis through suppression of NF-kappaB activation and IL-8 induction. Chalcones 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 22410118-0 2012 1,3-Diphenylpropenone ameliorates TNBS-induced rat colitis through suppression of NF-kappaB activation and IL-8 induction. Trinitrobenzenesulfonic Acid 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 22285171-7 2012 Dexamethasone pretreatment prior to LPS exposure significantly decreased IL-6 and IL-8 levels in both cell lines. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 22410118-1 2012 In the present study, we examined whether newly synthesized phenylpropenone derivatives, by inhibiting NF-kappaB activity, would inhibit IL-8 expression, inflammation and abnormal angiogenesis, resulting in amelioration of disease conditions. phenylpropenone 60-75 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 22410118-3 2012 Among the derivatives, 1,3-diphenylpropenone (DPhP) was most efficacious, and it significantly suppressed TNF-alpha-induced production of IL-8 which is a proinflammatory and proangiogenic cytokine. Chalcones 23-44 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 22410118-3 2012 Among the derivatives, 1,3-diphenylpropenone (DPhP) was most efficacious, and it significantly suppressed TNF-alpha-induced production of IL-8 which is a proinflammatory and proangiogenic cytokine. Chalcones 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 22410118-6 2012 In the colon tissue, DPhP inhibited TNBS-induced NF-kappaB nuclear translocation, IL-8 and TNF-alpha expressions, and abnormal angiogenesis. Chalcones 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 22410118-6 2012 In the colon tissue, DPhP inhibited TNBS-induced NF-kappaB nuclear translocation, IL-8 and TNF-alpha expressions, and abnormal angiogenesis. Trinitrobenzenesulfonic Acid 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 22410118-9 2012 In conclusion, the results suggest that DPhP is a potential dual-acting IBD drug candidate targeting both inflammation and abnormal angiogenesis, possibly through the NF-kappaB and IL-8 signaling pathway. Chalcones 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 22289904-6 2012 RESULTS: Pretreatment with dexamethasone led to a significant decrease in myocardial expression of IL-6, IL-8, IL-1beta, and TNF-alpha messenger RNA and to a decrease in protein synthesis of TNF-alpha. Dexamethasone 27-40 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 22565056-8 2012 In contrast, PGE(2) enhanced CXCL8 production early during maturation, whereas CXCL16 levels were continuously elevated, contributing to innate immune cell recruitment. Dinoprostone 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 29-34 21913898-8 2012 Roflumilast and roflumilast N-oxide concentration-dependently reduced the LPS-stimulated release of CCL2, CCL3, CCL4, CXCL10 and TNF-alpha from human lung macrophages, whereas that of CXCL1 or CXCL8 was not altered. n-oxide 28-35 C-X-C motif chemokine ligand 8 Homo sapiens 193-198 22315307-8 2012 SkMCs released IL-6, IL-8, and monocyte chemoattractant protein-1 on Hsp60 stimulation. skmcs 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 22189418-9 2012 These peptides similarly displaced the binding of (125)I-hCXCL8 to hCXCR1 (IC(50) ranging from 8.5 to 10muM) in a dose-dependent manner, inhibited hCXCL8 induced increases in the intracellular calcium, and migration of hCXCR1- and hCXCR2-transfected cells. Calcium 193-200 C-X-C motif chemokine ligand 8 Homo sapiens 57-63 22189418-9 2012 These peptides similarly displaced the binding of (125)I-hCXCL8 to hCXCR1 (IC(50) ranging from 8.5 to 10muM) in a dose-dependent manner, inhibited hCXCL8 induced increases in the intracellular calcium, and migration of hCXCR1- and hCXCR2-transfected cells. Calcium 193-200 C-X-C motif chemokine ligand 8 Homo sapiens 147-153 21848430-8 2012 We observed inhibition of cytokines (interleukin [IL]-1beta (beta), IL-6, IL-8, IL-10, and tumor necrosis factor-alpha) in the presence of azithromycin in EB-stimulated cells from both fertile and infertile women with primary and recurrent C. trachomatis infection. Azithromycin 139-151 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 22116002-6 2012 Poly(I:C) stimulated the secretion of IL-6, IL-8, MCP-1, RANTES, IP-10, eotaxin, MIP-1beta, and interferon-gamma, whereas zymosan triggered the production of IL-6, IL-8, and MCP-1. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 21885397-10 2012 Carbachol stimulated release of LTB(4) from lung macrophages (buffer 222.3 +- 75.1 versus carbachol 1,118 +- 622.4 pg mL(-1); n = 15, p<0.05) but not IL-6 or IL-8. Carbachol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 22116002-6 2012 Poly(I:C) stimulated the secretion of IL-6, IL-8, MCP-1, RANTES, IP-10, eotaxin, MIP-1beta, and interferon-gamma, whereas zymosan triggered the production of IL-6, IL-8, and MCP-1. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 22116002-6 2012 Poly(I:C) stimulated the secretion of IL-6, IL-8, MCP-1, RANTES, IP-10, eotaxin, MIP-1beta, and interferon-gamma, whereas zymosan triggered the production of IL-6, IL-8, and MCP-1. Zymosan 122-129 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 22116002-7 2012 LPS, poly(I:C), and zymosan thus each induced a distinct pattern of cytokine and chemokine release from human corneal fibroblasts, with the release of IL-6, IL-8, and MCP-1 being commonly elicited by all three agents. Poly I-C 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 22116002-7 2012 LPS, poly(I:C), and zymosan thus each induced a distinct pattern of cytokine and chemokine release from human corneal fibroblasts, with the release of IL-6, IL-8, and MCP-1 being commonly elicited by all three agents. Zymosan 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 22236730-9 2012 TNF-alpha (P < .05) and IL-8 fold suppression by dexamethasone (P < .05) were significantly reduced in PBMCs from SR asthmatic patients. Dexamethasone 52-65 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 22379967-10 2012 Finally, 5,7-DMF reduced IkappaBalpha phosphorylation, blocked NF-kappaB p65 nuclear translocation, strongly suppressed proinflammatory cytokines such as interleukin-6 (IL-6) and IL-8. 5,7-dimethoxyflavone 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 22192353-0 2012 Peroxisome proliferating activating receptor gamma-independent attenuation of interleukin 6 and interleukin 8 secretion from primary endometrial stromal cells by thiazolidinediones. Thiazolidinediones 162-180 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 22192353-8 2012 RESULT(S): Treatment of stromal cells with thiazolidinediones attenuated IL-6 and IL-8 release in a dose-dependent manner. Thiazolidinediones 43-61 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 22192353-11 2012 CONCLUSION(S): Thiazolidinediones decrease the proinflammatory cytokines IL-6 and IL-8 in endometrial stromal cells via a PPAR-gamma-independent mechanism. Thiazolidinediones 15-33 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 22158745-5 2012 In contrast, coculture of A549 cells with the macrophage-like THP-1 cell line, differentiated with vitamin D, or monocyte-derived macrophages enhanced CXCL8 release. Vitamin D 99-108 C-X-C motif chemokine ligand 8 Homo sapiens 151-156 21907687-11 2012 Lipid accumulation in hepatocytes, induced by incubation with fatty acids, was associated with increased CML formation and expression of the receptor for advanced glycation endproducts (RAGE), PAI-1, IL-8, IL-6, and CRP. Fatty Acids 62-73 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 21545687-5 2012 Tumour necrosis factor-alpha (TNF-alpha) significantly induced phosphorylation of p38 MAPK, ERK, Akt and production of IL-8 from HCC cells, which were prevented by SB203580 (p38 MAPK inhibitor), PD98059 (ERK inhibitor), LY294002 and Wortmannin (PI3K inhibitor) and SB328437 (CCR3 inhibitor). SB 203580 164-172 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 21545687-5 2012 Tumour necrosis factor-alpha (TNF-alpha) significantly induced phosphorylation of p38 MAPK, ERK, Akt and production of IL-8 from HCC cells, which were prevented by SB203580 (p38 MAPK inhibitor), PD98059 (ERK inhibitor), LY294002 and Wortmannin (PI3K inhibitor) and SB328437 (CCR3 inhibitor). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 195-202 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 21545687-5 2012 Tumour necrosis factor-alpha (TNF-alpha) significantly induced phosphorylation of p38 MAPK, ERK, Akt and production of IL-8 from HCC cells, which were prevented by SB203580 (p38 MAPK inhibitor), PD98059 (ERK inhibitor), LY294002 and Wortmannin (PI3K inhibitor) and SB328437 (CCR3 inhibitor). 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 220-228 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 21545687-5 2012 Tumour necrosis factor-alpha (TNF-alpha) significantly induced phosphorylation of p38 MAPK, ERK, Akt and production of IL-8 from HCC cells, which were prevented by SB203580 (p38 MAPK inhibitor), PD98059 (ERK inhibitor), LY294002 and Wortmannin (PI3K inhibitor) and SB328437 (CCR3 inhibitor). Wortmannin 233-243 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 21545687-5 2012 Tumour necrosis factor-alpha (TNF-alpha) significantly induced phosphorylation of p38 MAPK, ERK, Akt and production of IL-8 from HCC cells, which were prevented by SB203580 (p38 MAPK inhibitor), PD98059 (ERK inhibitor), LY294002 and Wortmannin (PI3K inhibitor) and SB328437 (CCR3 inhibitor). SB 328437 265-273 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 22325176-7 2012 In addition, DHMEQ inhibited IL-8 production induced by LPS in HT-29 cells. dehydroxymethylepoxyquinomicin 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 21907687-12 2012 Pyridoxamine and aminoguanidine inhibited the endogenous CML formation and the increased RAGE, PAI-1, IL-8, IL-6, and CRP expression. Pyridoxamine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21907687-12 2012 Pyridoxamine and aminoguanidine inhibited the endogenous CML formation and the increased RAGE, PAI-1, IL-8, IL-6, and CRP expression. pimagedine 17-31 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21698672-4 2012 An oily extract of ginger rhizome with > 25% total pungent compounds, ginger volatile oil, ar-curcumene and alpha-pinene reduced the LPS-induced IL-8 secretion (measured by a specific enzyme-linked immunosorbent assay), whereas a spissum extract, the pungents [6]-gingerol and its metabolite [6]-shogaol, and the terpenoids citral and beta-phellandrene showed no effect. alpha-curcumene 94-106 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 22309277-9 2012 CRSwNP cultures were more sensitive than controls to dexamethasone (1 microg/ml) dependent IL-6 and IL-8 suppression. Dexamethasone 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 21698672-4 2012 An oily extract of ginger rhizome with > 25% total pungent compounds, ginger volatile oil, ar-curcumene and alpha-pinene reduced the LPS-induced IL-8 secretion (measured by a specific enzyme-linked immunosorbent assay), whereas a spissum extract, the pungents [6]-gingerol and its metabolite [6]-shogaol, and the terpenoids citral and beta-phellandrene showed no effect. alpha-pinene 111-123 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21698672-4 2012 An oily extract of ginger rhizome with > 25% total pungent compounds, ginger volatile oil, ar-curcumene and alpha-pinene reduced the LPS-induced IL-8 secretion (measured by a specific enzyme-linked immunosorbent assay), whereas a spissum extract, the pungents [6]-gingerol and its metabolite [6]-shogaol, and the terpenoids citral and beta-phellandrene showed no effect. gingerol 267-275 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21698672-4 2012 An oily extract of ginger rhizome with > 25% total pungent compounds, ginger volatile oil, ar-curcumene and alpha-pinene reduced the LPS-induced IL-8 secretion (measured by a specific enzyme-linked immunosorbent assay), whereas a spissum extract, the pungents [6]-gingerol and its metabolite [6]-shogaol, and the terpenoids citral and beta-phellandrene showed no effect. shogaol 295-306 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21698672-4 2012 An oily extract of ginger rhizome with > 25% total pungent compounds, ginger volatile oil, ar-curcumene and alpha-pinene reduced the LPS-induced IL-8 secretion (measured by a specific enzyme-linked immunosorbent assay), whereas a spissum extract, the pungents [6]-gingerol and its metabolite [6]-shogaol, and the terpenoids citral and beta-phellandrene showed no effect. Terpenes 316-326 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21698672-4 2012 An oily extract of ginger rhizome with > 25% total pungent compounds, ginger volatile oil, ar-curcumene and alpha-pinene reduced the LPS-induced IL-8 secretion (measured by a specific enzyme-linked immunosorbent assay), whereas a spissum extract, the pungents [6]-gingerol and its metabolite [6]-shogaol, and the terpenoids citral and beta-phellandrene showed no effect. citral 327-333 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21698672-4 2012 An oily extract of ginger rhizome with > 25% total pungent compounds, ginger volatile oil, ar-curcumene and alpha-pinene reduced the LPS-induced IL-8 secretion (measured by a specific enzyme-linked immunosorbent assay), whereas a spissum extract, the pungents [6]-gingerol and its metabolite [6]-shogaol, and the terpenoids citral and beta-phellandrene showed no effect. beta-phellandrene 338-355 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 22611924-1 2012 OBJECTIVE: To investigate the effects of citreoviridin (CIT) on the expression of MCP-1, IL-1beta, IL-6 and IL-8 induced by TNF-alpha in human umbilical vein endothelial cells (HUVECs). citreoviridin 41-54 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 21161531-0 2012 Inhibitors of p38 and ERK1/2 MAPkinase and hydrogen sulphide block constitutive and IL-1beta-induced IL-6 and IL-8 expression in the human chondrocyte cell line C-28/I2. Hydrogen Sulfide 43-60 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 21161531-6 2012 Furthermore, IL-6 and IL-8 expression was quantified by real-time polymerase chain reaction (RT-PCR) and ELISAs from cells which were exposed to SB203580, U0126 and NaHS and stimulated by IL-1beta. SB 203580 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 21161531-6 2012 Furthermore, IL-6 and IL-8 expression was quantified by real-time polymerase chain reaction (RT-PCR) and ELISAs from cells which were exposed to SB203580, U0126 and NaHS and stimulated by IL-1beta. U 0126 155-160 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 21161531-6 2012 Furthermore, IL-6 and IL-8 expression was quantified by real-time polymerase chain reaction (RT-PCR) and ELISAs from cells which were exposed to SB203580, U0126 and NaHS and stimulated by IL-1beta. SODIUM HYDROSULFIDE 165-169 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 21161531-8 2012 The data provided prove that in these cells, constitutive as well as IL-1beta-induced IL-6 and IL-8 expression was partially and transiently blocked by the treatment of cells with both MAPK inhibitors and NaHS. SODIUM HYDROSULFIDE 205-209 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 22611924-6 2012 CONCLUSION: The expression of NF-kappaB, MCP-1, IL-1beta, IL-6 and IL-8 in HUVECs up-regulated by TNF-alpha was promoted by CIT. citreoviridin 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 22611924-1 2012 OBJECTIVE: To investigate the effects of citreoviridin (CIT) on the expression of MCP-1, IL-1beta, IL-6 and IL-8 induced by TNF-alpha in human umbilical vein endothelial cells (HUVECs). citreoviridin 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 22271561-0 2012 The myxobacterial compounds spirangien a and spirangien M522 are potent inhibitors of IL-8 expression. spirangien A 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 22800594-2 2012 METHODS: Nthy-ori 3-1 cells were exposed to 0.0, 0.1, 1.0, 3.0 mmol/L of sodium fluoride (NaF) in vitro. Sodium Fluoride 73-88 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 22271561-0 2012 The myxobacterial compounds spirangien a and spirangien M522 are potent inhibitors of IL-8 expression. spirangien M522 45-60 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 22074915-4 2012 We further show that blocking this channel perturbs the calcium homeostasis of the cells and inhibits the proliferation, production of VEGF, IL-8, and pro-MMP-2, and migration and invasion of RA-FLS. Calcium 56-63 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21917119-0 2012 Nonylphenol induces bronchial epithelial apoptosis via Fas-mediated pathway and stimulates bronchial epithelium to secrete IL-6 and IL-8, causing bronchial smooth muscle proliferation and migration. nonylphenol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 22558684-0 2012 Effect of bamboo salt-NaF dentifrice on enamel remineralization. bamboo salt 10-21 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 21989538-12 2012 Conditioned media from AAT and SM cultures similarly upregulated IL-6, IL-8, Dickkopf-1 and osteoprotegerin production by rheumatoid FLS. o-Aminoazotoluene 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 21969073-1 2012 We previously demonstrated in the human promyelocytic cell line THP-1 that all allergens tested, with the exception of the prohapten isoeugenol, induced a dose-related release of interleukin-8 (IL-8). prohapten isoeugenol 123-143 C-X-C motif chemokine ligand 8 Homo sapiens 179-192 21969073-1 2012 We previously demonstrated in the human promyelocytic cell line THP-1 that all allergens tested, with the exception of the prohapten isoeugenol, induced a dose-related release of interleukin-8 (IL-8). prohapten isoeugenol 123-143 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 21969073-7 2012 The increased expression of TTP in THP-1 cells treated with isoeugenol results in destabilization of the IL-8 mRNA, which can account for the lack of IL-8 release. isoeugenol 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 21969073-8 2012 In contrast, the strong allergen DNCB failing to up-regulate TTP, while inducing HuR, resulted in longer IL-8 mRNA half-life and protein release. Dinitrochlorobenzene 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 21969073-10 2012 Finally, the destabilization effect of isoeugenol on IL-8 mRNA expression together with SOCS-3 expression resulted in an anti-inflammatory effect, as demonstrated by the ability of isoeugenol to modulate LPS or ionomycin-induced cytokine release. isoeugenol 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 21969073-10 2012 Finally, the destabilization effect of isoeugenol on IL-8 mRNA expression together with SOCS-3 expression resulted in an anti-inflammatory effect, as demonstrated by the ability of isoeugenol to modulate LPS or ionomycin-induced cytokine release. Ionomycin 211-220 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 22231588-3 2012 We used isothermal titration calorimetry to measure the enthalpies of mixing, DeltaH(mix), of 3,3- and 6,6-ionene fluorides and bromides with low molecular weight salts (NaF, NaCl, NaBr, and NaI) at 298 K in water. Bromides 128-136 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 21917119-7 2012 Exposure of BEAS-2B and HBE to NP caused epithelial cells to produce inflammatory cytokines IL-6 and IL-8, which subsequently induced BSMC proliferation and migration. bsmc 134-138 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 21917119-8 2012 Depleting both IL-6 and IL-8 completely reversed the effect of NP-BEAS-2B-CM- and NP-HBE-CM-mediated BSMC proliferation and migration, suggesting that this effect is a synergistic influence of IL-6 and IL-8. bsmc 101-105 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 21917119-9 2012 This study is the first to demonstrate that NP not only induces bronchial epithelial apoptosis via the Fas-mediated pathway but also stimulates the bronchial epithelium to secrete IL-6 and IL-8, which cause bronchial smooth muscle proliferation and migration - major features in asthma remodelling. nonylphenol 44-46 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 22316209-7 2012 We examined the gene expression profile of two lung tumor cell lines to identify a shared gene signature in response to sublethal cisplatin/vinorelbine and found coordinate expression of only 16 transcripts, including those for cytokine/chemokine expression and apoptosis such as tumor necrosis factor-alpha, IL8, CXCL5, and B cell lymphoma-2-like genes (BCL-2). Cisplatin 130-139 C-X-C motif chemokine ligand 8 Homo sapiens 309-312 22490477-12 2012 Sufentanil consumption and plasma interleukin-8 levels at 2 and 12 hours postoperatively were significantly lower in the PA group than the C group (P < 0.05). Protactinium 121-123 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 21347606-9 2012 Dopamine doses were positively associated with IL-6, and norepinephrine was inversely associated with IL-8 and TNF-alpha levels. Norepinephrine 57-71 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21997482-8 2012 Catalase overexpression and inhibitors of mitochondrial respiration diminished elevations in IL-8 and COX-2 induced by exposure to 1,2-NQ, but potentiated HO-1 mRNA levels in BEAS cells. 1,2-naphthoquinone 131-137 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 21828034-3 2012 We investigated whether interleukin (IL)-17A induces GC insensitivity in airway epithelium by studying its effects on responsiveness of tumour necrosis factor (TNF)-alpha-induced IL-8 production to budesonide in human bronchial epithelial 16HBE cells. Budesonide 198-208 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 21828034-5 2012 We demonstrated that IL-17A-induced IL-8 production is normally sensitive to GCs, while IL-17A pre-treatment significantly reduced the sensitivity of TNF-alpha-induced IL-8 production to budesonide. Budesonide 187-197 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 21487907-5 2012 IL-8 levels were significantly higher in patients with pulmonary edema (1,829 +- 2,496 vs 456 +- 624 pg/ml, p < 0.05); sIL-2r, IL-6, and IL-8 levels were increased proportionally to Killip class (r = 0.35, p < 0.05; r = 0.48, r = 0.47, p < 0.01) and in patients with LV ejection fraction (LVEF) < 30%. killip 185-191 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21088047-11 2012 Inhibition of lipolysis by orlistat or CAY10499 reduced LPS-induced IL-6 and IL-8 mRNA expression. CAY 10499 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 22094458-0 2012 An NF-kappaB-independent and Erk1/2-dependent mechanism controls CXCL8/IL-8 responses of airway epithelial cells to cadmium. Cadmium 116-123 C-X-C motif chemokine ligand 8 Homo sapiens 65-70 22221101-0 2012 Transient receptor potential vanilloid-1 participates in the inhibitory effect of ginsenoside Rg1 on capsaicin-induced interleukin-8 and prostaglandin E2 production in HaCaT cells. Capsaicin 101-110 C-X-C motif chemokine ligand 8 Homo sapiens 119-132 22221101-8 2012 More importantly, GRg1 dose-dependently inhibited capsaicin-induced PGE(2) and IL-8 secretion in HaCaT cells and HEK 293T-TRPV1 cells. Capsaicin 50-59 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 21809384-4 2012 Effects of short-term treatment with IL-alpha, IL-6, or IL-8 on endogenous GTP-bound Cdc42 levels were assessed using an affinity assay, and on actin filament organization using confocal microscopy. Guanosine Triphosphate 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 21809384-6 2012 Short exposure to IL-1alpha, IL-6, or IL-8 decreased endogenous GTP-Cdc42 and increased stress fibers, which were reversed with cytochalasin D treatment. Guanosine Triphosphate 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 21809384-6 2012 Short exposure to IL-1alpha, IL-6, or IL-8 decreased endogenous GTP-Cdc42 and increased stress fibers, which were reversed with cytochalasin D treatment. Cytochalasin D 128-142 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 22239529-5 2012 Results revealed that while thalidomide reduced IL-8 and nuclear factor kappa B (NF-kappaB) activity by 95% and 46% in Huh-7 cells, increasing concentrations of thalidomide correlated with a linear rise in HCV replication (17-fold at 200 mum). Thalidomide 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 21998275-7 2012 Similar differences on MAPK activation and IL-8 cytokine release were also observed upon exposure of HEK293 cell transfectants expressing the A471V variants to Zymosan, a beta-glucan-rich fungal particle. Zymosan 160-167 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 22048642-0 2012 The role of MAPK and Nrf2 pathways in ketanserin-elicited attenuation of cigarette smoke-induced IL-8 production in human bronchial epithelial cells. Ketanserin 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 22048642-4 2012 In this study, we investigated the antioxidative and anti-inflammatory properties of ketanserin and its underlying mechanism of action on cigarette smoke-induced interleukin (IL)-8 release in vitro. Ketanserin 85-95 C-X-C motif chemokine ligand 8 Homo sapiens 162-180 22048642-10 2012 Ketanserin suppressed CSM-induced IL-8 release by inhibiting p38, ERK1/2 MAPK, and Nrf2 signaling pathways and partially inhibited CSM-induced reduction of rGSH/GSSG ratio. Ketanserin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 22094458-0 2012 An NF-kappaB-independent and Erk1/2-dependent mechanism controls CXCL8/IL-8 responses of airway epithelial cells to cadmium. Cadmium 116-123 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 22048642-7 2012 Consistently, CSM-induced IL-8 release was blocked by SB203580, U0126, or MEK1 small interfering RNA (siRNA) but not SP600125. SB 203580 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 22048642-7 2012 Consistently, CSM-induced IL-8 release was blocked by SB203580, U0126, or MEK1 small interfering RNA (siRNA) but not SP600125. U 0126 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 22094458-3 2012 To address the role of airway epithelial cells in cadmium-induced lung inflammation, we investigated how cadmium regulates secretion of interleukin 8 (IL-8) by airway epithelial cells. Cadmium 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 136-149 22094458-3 2012 To address the role of airway epithelial cells in cadmium-induced lung inflammation, we investigated how cadmium regulates secretion of interleukin 8 (IL-8) by airway epithelial cells. Cadmium 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 22094458-4 2012 We show that exposure of human airway epithelial cells to subtoxic doses of cadmium in vitro promotes a characteristic inflammatory cytokine response consisting of IL-8, but not IL-1beta or tumor necrosis factor-alpha. Cadmium 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 22094458-9 2012 However, only pharmacological inhibition of Erk1/2 pathway or knockdown of the expression of Erk1 and Erk2 using small interfering RNAs suppressed secretion of IL-8 induced by cadmium. Cadmium 176-183 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 22094458-10 2012 Our findings identify cadmium as a potent activator of the proinflammatory cytokine IL-8 in lung epithelial cells and reveal for the first time the role of an NF-kappaB-independent but Erk1/2-dependent pathway in cadmium-induced lung inflammation. Cadmium 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 22251280-1 2012 The interaction between nuclear graphite and molten fluoride salts (46.5 mol % LiF/11.5 mol % NaF/42 mol % KF) is investigated by synchrotron X-ray diffraction and C K-edge X-ray absorption near-edge structure (XANES). Graphite 32-40 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 22015639-10 2012 H(2)S-induced expression of IL-6, IL-8 and COX-2 was completely blocked by specific inhibitors of p38 and ERK1/2 MAPK and NF-kappaB. Hydrogen Sulfide 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 26448690-6 2012 Like dexamethasone RU24858 also reduced CXCL8 and MIP-1alpha. RU24858 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 40-45 26448690-8 2012 We have shown here that dexamethasone and RU24858 both increase Grb-2, BLT1 and Annexin-1 expression and inhibit CXCL8 and MIP-1alpha production. Dexamethasone 24-37 C-X-C motif chemokine ligand 8 Homo sapiens 113-118 26448690-8 2012 We have shown here that dexamethasone and RU24858 both increase Grb-2, BLT1 and Annexin-1 expression and inhibit CXCL8 and MIP-1alpha production. RU24858 42-49 C-X-C motif chemokine ligand 8 Homo sapiens 113-118 22251280-1 2012 The interaction between nuclear graphite and molten fluoride salts (46.5 mol % LiF/11.5 mol % NaF/42 mol % KF) is investigated by synchrotron X-ray diffraction and C K-edge X-ray absorption near-edge structure (XANES). Fluorides 52-66 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 22269218-8 2012 CONCLUSIONS: Gamma tocopherol supplementation increased IL-6, IL-8, and KDR mRNA abundances and suppressed sFlt1 and TNFalpha mRNA abundances thereby increased VEGF mRNA expression and angiogenesis in placental vascular network during late gestation. Tocopherols 19-29 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 22269218-9 2012 It is plausible that the angiogenic effect of gamma tocopherol in placental vascular network is exerted via an alternate path by enhancing IL-6 and IL-8. gamma-Tocopherol 46-62 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 22080750-0 2012 Prostaglandin E2 enhances interleukin-8 production via EP4 receptor in human pulmonary microvascular endothelial cells. Dinoprostone 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 26-39 22080750-2 2012 This study investigated whether PGE(2) can induce production of interleukin (IL)-8, the major chemokine for neutrophil activation, from human pulmonary microvascular endothelial cells (HPMVECs). Prostaglandins E 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 64-82 22080750-3 2012 PGE(2) significantly enhanced IL-8 protein production with increases in IL-8 mRNA expression and intracellular cAMP levels. Prostaglandins E 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 22080750-3 2012 PGE(2) significantly enhanced IL-8 protein production with increases in IL-8 mRNA expression and intracellular cAMP levels. Prostaglandins E 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 22080750-7 2012 PGE(2)-induced IL-8 production was accompanied by p38 phosphorylation and was significantly inhibited by a p38 inhibitor, SB-203580, but not by an ERK1/2 inhibitor, U-0126, or a JNK inhibitor, SP-600125. Dinoprostone 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 22080750-7 2012 PGE(2)-induced IL-8 production was accompanied by p38 phosphorylation and was significantly inhibited by a p38 inhibitor, SB-203580, but not by an ERK1/2 inhibitor, U-0126, or a JNK inhibitor, SP-600125. SB 203580 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 22080750-7 2012 PGE(2)-induced IL-8 production was accompanied by p38 phosphorylation and was significantly inhibited by a p38 inhibitor, SB-203580, but not by an ERK1/2 inhibitor, U-0126, or a JNK inhibitor, SP-600125. pyrazolanthrone 193-202 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 22080750-9 2012 In conclusion, PGE(2) enhances IL-8 production via EP4 receptor coupled to G(s) protein in HPMVECs. Prostaglandins E 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 22080750-11 2012 Because neutrophils play a critical role in the inflammation of acute lung injury/acute respiratory distress syndrome, IL-8 released from the pulmonary microvasculature in response to PGE(2) may contribute to pathophysiology of this disease. Prostaglandins E 184-187 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 22020518-5 2012 Moreover, the spaCBA mutant induces an elevated level of interleukin-8 (IL-8) mRNA in Caco-2 cells compared to the wild type, possibly involving an interaction of lipoteichoic acid with Toll-like receptor 2. lipoteichoic acid 163-180 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 22230722-2 2012 It was the aim of this clinical study to assess the fluoride content, provided by NaF compared to amine fluoride, in saliva and plaque. Fluorides 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 23227796-6 2012 In addition, AMC decreased gene expression and secretion of proinflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6 and IL-8 in human mast cells. 7-amino-4-methylcoumarin 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 22239975-4 2012 In this study we show in human PBMCs that LPS stimulated proinflammatory cytokine release (CXCL8 and IL6) was inhibited by approximately 50% by the broad specificity phosphatidylinositol 3-kinase (PI3K) inhibitor, wortmannin. Wortmannin 214-224 C-X-C motif chemokine ligand 8 Homo sapiens 91-96 22142850-3 2012 Here we show that exposure of human airway epithelial cells to cadmium promotes a polarized apical secretion of IL-6 and IL-8, two pivotal pro-inflammatory cytokines known to play an important role in pulmonary inflammation. Cadmium 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 22142850-4 2012 We also determined that two distinct pathways controlled secretion of these proinflammatory cytokines by human airway epithelial cells as cadmium-induced IL-6 secretion occurs via an NF-kappaB dependent pathway, whereas IL-8 secretion involves the Erk1/2 signaling pathway. Cadmium 138-145 C-X-C motif chemokine ligand 8 Homo sapiens 220-224 22142850-5 2012 Interestingly, the natural antioxidant curcumin could prevent both cadmium-induced IL-6 and IL-8 secretion by human airway epithelial cells. Curcumin 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 22142850-5 2012 Interestingly, the natural antioxidant curcumin could prevent both cadmium-induced IL-6 and IL-8 secretion by human airway epithelial cells. Cadmium 67-74 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 23383400-4 2012 At baseline, PBMCs of four sALS patients (Group 1) showed significantly increased expression of TLR2 and CD14; ALOX5, PTGS2 and MMP1; IL1alpha, IL1beta, IL6, IL36G, IL8 and TNF; CCL3, CCL20, CXCL2, CXCL3 and CXCL5. sals 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 165-168 21714724-7 2012 INNOVATION: Our observation in this study reveals that flagellin-induced hydrogen peroxide (H(2)O(2)) generation is critical for TLR5-dependent innate immune responses, including IL-8 production and MUC5AC expression in the nasal epithelium. Hydrogen Peroxide 73-90 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 22020518-5 2012 Moreover, the spaCBA mutant induces an elevated level of interleukin-8 (IL-8) mRNA in Caco-2 cells compared to the wild type, possibly involving an interaction of lipoteichoic acid with Toll-like receptor 2. lipoteichoic acid 163-180 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 21818627-7 2012 Akt and NF-kappaB related inflammatory cytokine IL-1alpha, and IL-6 and the chemokine IL-8 were upregulated in treated cells at 6 and 24 h. The calpain inhibitor leupeptin limited Akt phosphorylation to Ser(473) and reduced release of IL-1alpha, IL-6, and IL-8, indicating that calpain or similar protease(s) are involved in PM-induced activation of Akt and subsequent release of inflammatory cytokines. leupeptin 162-171 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 21818627-7 2012 Akt and NF-kappaB related inflammatory cytokine IL-1alpha, and IL-6 and the chemokine IL-8 were upregulated in treated cells at 6 and 24 h. The calpain inhibitor leupeptin limited Akt phosphorylation to Ser(473) and reduced release of IL-1alpha, IL-6, and IL-8, indicating that calpain or similar protease(s) are involved in PM-induced activation of Akt and subsequent release of inflammatory cytokines. leupeptin 162-171 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 22020518-6 2012 In contrast, an L. rhamnosus GG mutant without exopolysaccharides but with an increased exposure of pili leads to the reduced expression of IL-8. exopolysaccharides 47-65 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 22020518-8 2012 Taken together, our data suggest that L. rhamnosus GG SpaCBA pili, while promoting strong adhesive interactions with IECs, have a functional role in balancing IL-8 mRNA expression induced by surface molecules such as lipoteichoic acid. lipoteichoic acid 217-234 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 22086137-9 2012 Our results show that high glucose concentrations (12 mM and particularly 24 mM) alter the biomineralization process in osteoblastic cells and provoke the following: i) a rise in mineralization, ii) an increase in the mRNA expression of RANKL and a decrease of OPG, iii) an increase in the mRNA expression of osteocalcin, bone sialoprotein and the transcription factor Runx2, iv) a diminished quality of the mineral, and v) an increase in the expression of IL1beta, IL6, IL8, MCP-1 and IL10 mRNAs. Glucose 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 471-474 21835900-8 2012 Treatment with methylprednisolone, compared with placebo, was associated with a statistically significant reduction in plasma IL-6 and IL-8, a significant increase in plasma IL-10, and a significant reduction in postoperative IL-1ra and IL-6, but not IL-8 in BAL fluid obtained 1 day after surgery. Methylprednisolone 15-33 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 23306224-2 2012 This study evaluated the surface of commercially pure titanium (cpTi) after exposure to different concentrations of sodium fluoride (NaF). Titanium 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 133-136 23306224-2 2012 This study evaluated the surface of commercially pure titanium (cpTi) after exposure to different concentrations of sodium fluoride (NaF). Sodium Fluoride 116-131 C-X-C motif chemokine ligand 8 Homo sapiens 133-136 23306224-3 2012 The hypothesis tested in this study was that different concentrations of NaF applied at different time intervals can affect the titanium surface in different ways. Titanium 128-136 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 23306224-11 2012 SEM micrographs showed that the titanium surface exposed to NaF presented corrosion that varied with the different concentrations. Titanium 32-40 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 21835900-8 2012 Treatment with methylprednisolone, compared with placebo, was associated with a statistically significant reduction in plasma IL-6 and IL-8, a significant increase in plasma IL-10, and a significant reduction in postoperative IL-1ra and IL-6, but not IL-8 in BAL fluid obtained 1 day after surgery. Methylprednisolone 15-33 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 22629114-9 2012 Together with LPS, adding gelatin tannate at different concentrations induced a dose-dependent inhibition of IL-8 and TNF-alpha released by Caco-2 cells. gelatin tannate 26-41 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 23113413-4 2012 Concentrations of IL-1beta, IL-6 and IL-8 related to creatinine levels (pg/micromol) were determined in urine samples in all. Creatinine 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 23113413-8 2012 However, IL-8/creatinine levels were almost significant higher in case group (median 3.5 pg/micromol; SD 9.2) than in control group (median 1.54 pg/micromol; SD 3) (P=0.001). Creatinine 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 23113413-10 2012 CONCLUSIONS: Urinary levels of IL-8/creatinine are elevated in children with vesicoureteral reflux, even in absence of urinary tract infection. Creatinine 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 22132892-7 2012 The findings showed a high responsiveness of monocytes through CCL2/CXCL8 expression, contributing to the creation of a proinflammatory environment in CIU. n-cyclohexyl-n'-(4-iodophenyl)urea 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 68-73 22785256-7 2012 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from THP-1 cells was significantly increased by the treatment of AMD or DEA with CYP3A4. desethylamiodarone 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 22387484-8 2012 CONCLUSIONS: We conclude that the NO-donor FK-409 improves the microcirculation by increasing the deformability of IL-8 activated PMN. FK 409 43-49 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 22675954-6 2012 The increase in IL-8 production by IL-1alpha or TNF-alpha was further enhanced by simultaneous addition of C2-ceramide. N-acetylsphingosine 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 22675954-7 2012 The increase of IL-8 stimulated by IL-1alpha or TNF-alpha was also suppressed by treatment with U0126 or SB203580. U 0126 96-101 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 22675954-7 2012 The increase of IL-8 stimulated by IL-1alpha or TNF-alpha was also suppressed by treatment with U0126 or SB203580. SB 203580 105-113 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 22675954-8 2012 The results of this study demonstrate that the production of IL-8 induced by IL-1alpha and TNF-alpha is enhanced by C2-ceramide, and suppressed by MEK inhibitor or P38 MAP kinase inhibitor. N-acetylsphingosine 116-127 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 22785256-8 2012 Similarly, IL-8 and TNFalpha were also upregulated by the treatment of AMD and DEA with human liver microsomes, but were inhibited by adding ketoconazole to the cell culture. Ketoconazole 141-153 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 22152986-0 2012 N-Aryl-2-phenyl-2,3-dihydro-imidazo[1,2-b]pyrazole-1-carboxamides 7-substituted strongly inhibiting both fMLP-OMe- and IL-8-induced human neutrophil chemotaxis. n-aryl-2-phenyl-2,3-dihydro-imidazo[1,2-b]pyrazole-1-carboxamides 0-65 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 22186417-9 2012 Cotreatment with LPS and sodium propionate decreased LPS-induced expression of inflammatory genes including IL-6, IL-8, cyclooxygenase-2, IL-1alpha, intercellular adhesion molecule-1, and platelet endothelial cell adhesion molecule-1 but not IL-1beta or lymphocyte function-associated antigen-1. sodium propionate 25-42 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 22186417-10 2012 Sodium propionate reduced LPS-induced neutrophil chemotaxis and protein secretion of the neutrophil chemoattractant IL-8. sodium propionate 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 22723766-6 2012 The maximal inhibition of H(2)O(2)-induced IL-8 secretion was greater with 2000 microg mL(-1) of pWPI (50%) vs. nWPI (30%) hydrolysates. Hydrogen Peroxide 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 23049614-9 2012 At the molecular level, acacetin significantly reduced IL-6, IL-8, intercellular adhesion molecule-1, and eotaxin-1 in activated BEAS-2B cells. acacetin 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 22082188-0 2012 Oligodeoxynucleotides inhibit Toll-like receptor 3 mediated cytotoxicity and CXCL8 release in keratinocytes. Oligodeoxyribonucleotides 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 77-82 22723766-6 2012 The maximal inhibition of H(2)O(2)-induced IL-8 secretion was greater with 2000 microg mL(-1) of pWPI (50%) vs. nWPI (30%) hydrolysates. pwpi 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 22154580-7 2012 Risperidone increased the production of IL-10 and MDC as well as the proinflammatory cytokines, such as IL-6, IL-8, and TNF-alpha, but decreased the production of IP-10 and IL-12. Risperidone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 22414682-5 2012 RESULTS: The levels of IL-8 and GRO-alpha were significantly increased after treatment with EGF, TGF-alpha, TNF-alpha and TPA by primary cultured granulosa-lutein cells. Tetradecanoylphorbol Acetate 122-125 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 22032841-9 2012 Dexamethasone had less suppressive effect on TNFalpha and CXCL8 production in vitro by neutrophils from induced sputum compared to neutrophils from paired blood samples. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 58-63 22132000-4 2012 We performed a genetic association study between IL8-251 (rs4073) and IL1B-511 (rs16944) polymorphisms in AERD, aspirin-tolerant asthma (ATA), and healthy control subjects. Aspirin 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 22792109-3 2012 This study compared the effectiveness of GaAlAs diode laser alone and with topical sodium fluoride gel (NaF). Sodium Fluoride 83-98 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 22919389-6 2012 The positive control solution (saturated hydroxyapatite solution) and 4500 mg/L fluoride as NaF significantly increased nanohardness D1-T by 19.9% and 24.1%, respectively, whereas 1400 mg/L fluoride as NaF, casein phosphopeptide-amorphous calcium phosphate mousse and negative control (deionised water) had no significant effect. Fluorides 80-88 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 22919389-6 2012 The positive control solution (saturated hydroxyapatite solution) and 4500 mg/L fluoride as NaF significantly increased nanohardness D1-T by 19.9% and 24.1%, respectively, whereas 1400 mg/L fluoride as NaF, casein phosphopeptide-amorphous calcium phosphate mousse and negative control (deionised water) had no significant effect. Fluorides 80-88 C-X-C motif chemokine ligand 8 Homo sapiens 202-205 22919389-6 2012 The positive control solution (saturated hydroxyapatite solution) and 4500 mg/L fluoride as NaF significantly increased nanohardness D1-T by 19.9% and 24.1%, respectively, whereas 1400 mg/L fluoride as NaF, casein phosphopeptide-amorphous calcium phosphate mousse and negative control (deionised water) had no significant effect. Fluorides 190-198 C-X-C motif chemokine ligand 8 Homo sapiens 202-205 22919389-6 2012 The positive control solution (saturated hydroxyapatite solution) and 4500 mg/L fluoride as NaF significantly increased nanohardness D1-T by 19.9% and 24.1%, respectively, whereas 1400 mg/L fluoride as NaF, casein phosphopeptide-amorphous calcium phosphate mousse and negative control (deionised water) had no significant effect. calcium phosphate 239-256 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 22919389-6 2012 The positive control solution (saturated hydroxyapatite solution) and 4500 mg/L fluoride as NaF significantly increased nanohardness D1-T by 19.9% and 24.1%, respectively, whereas 1400 mg/L fluoride as NaF, casein phosphopeptide-amorphous calcium phosphate mousse and negative control (deionised water) had no significant effect. Water 296-301 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 22837805-5 2012 RESULTS: KPV and gammaMSH evoked a dose-dependent inhibition of NFkappaB, matrix metalloproteinase-9 activity, IL8 and eotaxin secretion. 5-Phenyl-2-Keto-Valeric Acid 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 22627375-4 2012 We have observed that in the absence of eosinophil chemoattractants, neutrophils stimulated by IL-8 augment eosinophil trans-basement membrane migration by releasing superoxide anion, matrix metalloproteinase, leukotriene B(4) and platelet-activating factor. Superoxides 166-182 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 22627375-4 2012 We have observed that in the absence of eosinophil chemoattractants, neutrophils stimulated by IL-8 augment eosinophil trans-basement membrane migration by releasing superoxide anion, matrix metalloproteinase, leukotriene B(4) and platelet-activating factor. Leukotriene B4 210-223 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 21971406-5 2012 At baseline, increased hi-PA in normals predicted lower CSF levels of tau (r = -0.54, p = 0.020) and IL-8 (r = -0.70, p = 0.025). hi-pa 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 21691053-8 2012 Endosomal TLR3 inhibition by chloroquine dose-dependently inhibited dsRNA-induced TSLP generation and reduced generation of CXCL8, TNF-alpha, and IFN-beta. Chloroquine 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 124-129 22102722-3 2012 In this study, we found that MSU crystals, through P2Y(6) receptors, stimulated normal human keratinocytes (NHK) to produce IL-1alpha, IL-8/CXCL8, and IL-6. Uric Acid 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 22102722-3 2012 In this study, we found that MSU crystals, through P2Y(6) receptors, stimulated normal human keratinocytes (NHK) to produce IL-1alpha, IL-8/CXCL8, and IL-6. Uric Acid 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 140-145 22102722-5 2012 Both P2Y(6)-specific antagonist and P2Y(6) antisense oligonucleotides significantly inhibited the production of IL-1alpha, IL-8/CXCL8, and IL-6 by NHK. Oligonucleotides 53-69 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 22102722-5 2012 Both P2Y(6)-specific antagonist and P2Y(6) antisense oligonucleotides significantly inhibited the production of IL-1alpha, IL-8/CXCL8, and IL-6 by NHK. Oligonucleotides 53-69 C-X-C motif chemokine ligand 8 Homo sapiens 128-133 21412767-5 2012 EGF-stimulated IL-8 production, phosphorylation of Akt and Erk, and cell proliferation and movement could be inhibited by EGFR inhibitor (Erlotinib), PI3K inhibitor (GDC-0941 BEZ-235 and SHBM1009), and ERK1/2 inhibitor (PD98059). Erlotinib Hydrochloride 138-147 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 21753779-6 2012 Tumor necrosis factor-alpha- and benzo(a)pyrene (BaP)-induced reactive oxidative species (ROS) and IL-8 production were effectively inhibited by KCZ. Benzo(a)pyrene 33-47 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 21753779-6 2012 Tumor necrosis factor-alpha- and benzo(a)pyrene (BaP)-induced reactive oxidative species (ROS) and IL-8 production were effectively inhibited by KCZ. Benzo(a)pyrene 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 21753779-6 2012 Tumor necrosis factor-alpha- and benzo(a)pyrene (BaP)-induced reactive oxidative species (ROS) and IL-8 production were effectively inhibited by KCZ. Ketoconazole 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 23206461-9 2012 CONCLUSIONS: Preincisional parecoxib administration reduced postoperative pain and morphine consumption compared with postincisional administration, and attenuated IL-6 and IL-8 production 24 h after hip replacement surgery. parecoxib 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 22906259-0 2012 Wortmannin reduces metastasis and angiogenesis of human breast cancer cells via nuclear factor-kappaB-dependent matrix metalloproteinase-9 and interleukin-8 pathways. Wortmannin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 143-156 22906259-1 2012 OBJECTIVE: To investigate whether inhibition of Akt phosphorylation by the phosphatidylinositol 3-kinase (PI3K) inhibitor, wortmannin, reduces metastasis and angiogenesis in a human breast cancer cell line via nuclear factor (NF)-kappaB-dependent matrix metalloproteinase (MMP)-9 and interleukin (IL)-8 pathways. Wortmannin 123-133 C-X-C motif chemokine ligand 8 Homo sapiens 284-302 22988345-7 2012 TNF-alpha treatment of IECs resulted in an association between EGFR and HER2 and inhibition of HER2 using a specific inhibitor AG879 in combination with AG1478-suppressed TNF-alpha-dependent ERK phosphorylation and IL-8 release. AG-879 127-132 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 22906259-6 2012 RESULTS: Wortmannin inhibited the phosphorylation of Akt, upregulation of NF-kappaB, MMP-9, IL-8, and in vitro cell invasion and angiogenesis, in a dose-dependent manner. Wortmannin 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 22906259-9 2012 CONCLUSION: The findings of the present study suggest that wortmannin inhibits metastasis and angiogenesis in breast cancer cells via PI3K/Akt/NF-kappaB-mediated MMP-9 and IL-8 signalling pathways. Wortmannin 59-69 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 22363103-0 2012 Low dose theophylline showed an inhibitory effect on the production of IL-6 and IL-8 in primary lung fibroblast from patients with COPD. Theophylline 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 22363103-6 2012 For COPD fibroblasts, the protein levels of IL-6 and IL-8 decreased from 993.0 +- 738.9 pg/mL to 650.1 +- 421.9 pg/mL (P = 0.014) and from 703.1 +- 278.0 pg/mL to 492.0 +- 214.9 pg/mL (P = 0.001), respectively, with 5 mug/mL theophylline treatment. Theophylline 225-237 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 22363103-7 2012 In addition, theophylline at the dose of 5 mug/mL reduced the increased production of IL-6 and IL-8 induced by 1 mug/mL LPS in primary human lung fibroblasts. Theophylline 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 22719178-6 2012 Much data showed that macrolides reduced viral titers of RV ICAM-1, which is the receptor for RV, and RV infection-induced cytokines including IL-1beta, IL-6, IL-8, and TNF-alpha. Macrolides 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 22988345-7 2012 TNF-alpha treatment of IECs resulted in an association between EGFR and HER2 and inhibition of HER2 using a specific inhibitor AG879 in combination with AG1478-suppressed TNF-alpha-dependent ERK phosphorylation and IL-8 release. RTKI cpd 153-159 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 22761540-3 2012 Clarithromycin (CAM), which is an antimicrobial agent and is also known as an immunomodulator, significantly suppressed RSV-induced production of interleukin-6, interleukin-8, and regulated on activation, normal T-cell expressed and secreted (RANTES). Clarithromycin 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 21830064-8 2012 These results suggest that H2O2 upregulates the expression of ZNF580 via the NF-kappaB signaling pathway, and overexpression of ZNF580 plays a critical role in augmenting the release of pro-inflammatory cytokine IL-8. Hydrogen Peroxide 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 22761540-3 2012 Clarithromycin (CAM), which is an antimicrobial agent and is also known as an immunomodulator, significantly suppressed RSV-induced production of interleukin-6, interleukin-8, and regulated on activation, normal T-cell expressed and secreted (RANTES). Clarithromycin 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 21956503-4 2012 We show that hydrogen peroxide-induced oxidative stress can cause a ~twofold decrease in the number of lymphocytes secreting the TH1 cytokines IFN-gamma and IL-2, as well as chemokines IL-8 and TNF-alpha. Hydrogen Peroxide 13-30 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 23093820-9 2012 Comparison of the dose-dependent inhibition of chemokine (IL-8, IP-10, MCP-1) and growth factor (GM-CSF) release from PHK activated by TNFalpha + IFNgamma showed that leontopodic acid was mainly responsible for the inhibitory effects of ECC55. leontopodic acid 167-183 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 22355254-9 2012 Duration of topical Timolol and Alphagan therapy correlated negatively with CXCL8 (r=-0.588, p=0.035), respectively. Timolol 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 76-81 21999396-4 2012 Among the constituents, matrine, baicalin, ursolic acid, sodium danshensu, magnolol, honokiol, hesperidin and andrographolide significantly reduced IL-8 and TNF-alpha by human HaCaT keratinocyte cells pretreated with heat-killed P. acnes. matrine 24-31 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 22605930-10 2012 Interestingly, Travatan and Systane Ultra activated NF-kappaB and elevated the secretion of inflammation markers IL-6 by 3 to eightfold and IL-8 by 1.5 to 3.5 fold, respectively, as analyzed with ELISA. Travoprost 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 22605930-10 2012 Interestingly, Travatan and Systane Ultra activated NF-kappaB and elevated the secretion of inflammation markers IL-6 by 3 to eightfold and IL-8 by 1.5 to 3.5 fold, respectively, as analyzed with ELISA. SCHEMBL21048105 28-35 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 21999396-4 2012 Among the constituents, matrine, baicalin, ursolic acid, sodium danshensu, magnolol, honokiol, hesperidin and andrographolide significantly reduced IL-8 and TNF-alpha by human HaCaT keratinocyte cells pretreated with heat-killed P. acnes. andrographolide 110-125 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21999396-4 2012 Among the constituents, matrine, baicalin, ursolic acid, sodium danshensu, magnolol, honokiol, hesperidin and andrographolide significantly reduced IL-8 and TNF-alpha by human HaCaT keratinocyte cells pretreated with heat-killed P. acnes. baicalin 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21999396-4 2012 Among the constituents, matrine, baicalin, ursolic acid, sodium danshensu, magnolol, honokiol, hesperidin and andrographolide significantly reduced IL-8 and TNF-alpha by human HaCaT keratinocyte cells pretreated with heat-killed P. acnes. ursolic acid 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21999396-4 2012 Among the constituents, matrine, baicalin, ursolic acid, sodium danshensu, magnolol, honokiol, hesperidin and andrographolide significantly reduced IL-8 and TNF-alpha by human HaCaT keratinocyte cells pretreated with heat-killed P. acnes. Sodium Danshensu 57-73 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21999396-4 2012 Among the constituents, matrine, baicalin, ursolic acid, sodium danshensu, magnolol, honokiol, hesperidin and andrographolide significantly reduced IL-8 and TNF-alpha by human HaCaT keratinocyte cells pretreated with heat-killed P. acnes. magnolol 75-83 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21999396-4 2012 Among the constituents, matrine, baicalin, ursolic acid, sodium danshensu, magnolol, honokiol, hesperidin and andrographolide significantly reduced IL-8 and TNF-alpha by human HaCaT keratinocyte cells pretreated with heat-killed P. acnes. honokiol 85-93 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21999396-4 2012 Among the constituents, matrine, baicalin, ursolic acid, sodium danshensu, magnolol, honokiol, hesperidin and andrographolide significantly reduced IL-8 and TNF-alpha by human HaCaT keratinocyte cells pretreated with heat-killed P. acnes. Hesperidin 95-105 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 22973975-7 2012 Preincubation of Detroit cells with 200 muM curcumin for 5 to 60 min resulted in complete suppression of the release of tumor necrosis factor-alpha, interleukin (IL)-6, IL-8, monocyte chemoattractant protein 1, granulocyte macrophage-colony stimulating factor, and vascular endothelial growth factor. Curcumin 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 23051896-0 2012 Dopamine agonists upregulate IL-6 and IL-8 production in human keratinocytes. Dopamine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 23051896-8 2012 RESULTS: Dopamine stimulated the production of IL-6 and IL-8 in a concentration-dependent manner. Dopamine 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 23051896-11 2012 The latter drug was able to block the effect of dopamine on the secretion of IL-8. Dopamine 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 21958850-0 2012 Synthesis of [11C]interleukin 8 using a cell-free translation system and L-[11C]methionine. Carbon-11 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 21958850-0 2012 Synthesis of [11C]interleukin 8 using a cell-free translation system and L-[11C]methionine. l-[11c]methionine 73-90 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 21925926-13 2012 Taken together, LPA may be a potent inducer of osteolytic factor IL-6 and IL-8 in OSCC. lysophosphatidic acid 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 21958850-5 2012 In this study, [(11)C]interleukin 8 (IL-8; MW 9.2 kDa) was successfully synthesized by the cell-free system in combination with l-[(11)C]methionine. l-[(11)c]methionine 128-147 C-X-C motif chemokine ligand 8 Homo sapiens 15-35 21958850-5 2012 In this study, [(11)C]interleukin 8 (IL-8; MW 9.2 kDa) was successfully synthesized by the cell-free system in combination with l-[(11)C]methionine. l-[(11)c]methionine 128-147 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 21925926-14 2012 LPA-induced IL-6 and IL-8 exerted propound effects on RANKL expression in osteoblast and thereby promoted osteoclast formation from osteoclast precursors. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 21925926-0 2012 Secretion of IL-6 and IL-8 from lysophosphatidic acid-stimulated oral squamous cell carcinoma promotes osteoclastogenesis and bone resorption. lysophosphatidic acid 32-53 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 21925926-6 2012 LPA induced the secretion of IL-6 and IL-8 in oral squamous cell carcinoma (OSCC). lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 22952917-6 2012 PBMCs from patients with ASA produce typically less IL-13, IL-7, IL-17 and MIG, and more MIP-1beta and IL-8, as compared to PBMCs from patients without ASA. Aspirin 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 21925926-7 2012 LPA-stimulated secretion of IL-6 and IL-8 is partly dependent on the LPA and EGF receptor (EGFR) pathways. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 21925926-8 2012 ERK1/2 and Akt-mediated NF-kappaB and AP-1 were responsible for the LPA-induced IL-6 and IL-8 secretion. lysophosphatidic acid 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 21925926-10 2012 Neutralization against both human IL-6 and IL-8 suppressed osteoclast formation induced by CM derived from the LPA-stimulated OSCC. lysophosphatidic acid 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 21925926-11 2012 Direct treatment with recombinant IL-6 (rIL-6) and/or soluble IL-6 receptor (sIL-6R), or IL-8 (rIL-8) reproduced the effect of the CM derived from the LPA-stimulated OSCC on osteoclast formation. lysophosphatidic acid 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 23272151-6 2012 Likewise, stimulation of autophagy by nutrient starvation or rapamycin treatment reduced intracellular AIEC survival and IL-8 production. Sirolimus 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 23110185-8 2012 Treatment of neutrophils from healthy subjects with TNFalpha, IL-1beta, or IL-8 enhanced free radicals generation and NETs formation, which was mediated through the activation of NADPH oxidase and MPO. Free Radicals 89-102 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 23028541-13 2012 Over 97% of PSS samples were distinguished from controls by elevated CXCL10 (>500 ng/mL), CXCL8 (>30 ng/mL) and CCL2 (>60 ng/mL) levels. pss 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 22685620-5 2012 There was a significant decrease in IL-8 release from PBLs stimulated with H(2)O(2) incubated with (U), (C), (C&D), and (STD) herbs and from Caco-2 cells stimulated with TNFalpha incubated with (C&D) and (STD) herbs. Adenosine Monophosphate 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 22936990-1 2012 CXCR1, a classic GPCR that binds IL-8, plays a key role in neutrophil activation and migration by activating phospholipase C (PLC)beta through Galpha(15) and Galpha(i) which generates diacylglycerol and inositol phosphates (IPs). Diglycerides 184-198 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 22916253-11 2012 Moreover, we found that both LPS and CpG oligodeoxynucleotides (ODN) induced robust pro-inflammatory responses in thrombocytes, as characterized by more than 100 fold increase in interleukin (IL)-1beta, IL-6 and IL-8 transcripts, while only LPS enhanced nitric oxide production and phagocytic capabilities. CPG-oligonucleotide 37-62 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 22936990-1 2012 CXCR1, a classic GPCR that binds IL-8, plays a key role in neutrophil activation and migration by activating phospholipase C (PLC)beta through Galpha(15) and Galpha(i) which generates diacylglycerol and inositol phosphates (IPs). Inositol Phosphates 203-222 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 22936990-1 2012 CXCR1, a classic GPCR that binds IL-8, plays a key role in neutrophil activation and migration by activating phospholipase C (PLC)beta through Galpha(15) and Galpha(i) which generates diacylglycerol and inositol phosphates (IPs). Inositol Phosphates 224-227 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 22815786-6 2012 Atorvastatin increased the intracellular contents of GRO-alpha, IL-8, and MCP-1 and induced colocalization with E-selectin in multivesicular bodies. Atorvastatin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 22911818-4 2012 METHODOLOGY/PRINCIPAL FINDINGS: Corticosteroid sensitivity was determined by measuring dexamethasone inhibition of CD3/28 and TNF-alpha induced IL-8 production in PBMCs by using ELISA. Dexamethasone 87-100 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 22479453-0 2012 Methamphetamine increases LPS-mediated expression of IL-8, TNF-alpha and IL-1beta in human macrophages through common signaling pathways. Methamphetamine 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 22590561-4 2012 RESULTS: Administration of 5-FU but not pemetrexed potentiated CXCL8 secretion and increased CXCR1 and CXCR2 gene expression in metastatic PC3 cells. Fluorouracil 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 63-68 22590561-5 2012 Consistent with this, the inhibition of CXCL8 signaling using a CXCR2 antagonist, AZ10397767, increased the cytotoxicity of 5-FU by 4-fold (P<0.001), and increased 5-FU-induced apoptosis in PC3 cells (P<0.01). AZ10397767 82-92 C-X-C motif chemokine ligand 8 Homo sapiens 40-45 22590561-5 2012 Consistent with this, the inhibition of CXCL8 signaling using a CXCR2 antagonist, AZ10397767, increased the cytotoxicity of 5-FU by 4-fold (P<0.001), and increased 5-FU-induced apoptosis in PC3 cells (P<0.01). Fluorouracil 124-128 C-X-C motif chemokine ligand 8 Homo sapiens 40-45 22590561-5 2012 Consistent with this, the inhibition of CXCL8 signaling using a CXCR2 antagonist, AZ10397767, increased the cytotoxicity of 5-FU by 4-fold (P<0.001), and increased 5-FU-induced apoptosis in PC3 cells (P<0.01). Fluorouracil 167-171 C-X-C motif chemokine ligand 8 Homo sapiens 40-45 22590561-8 2012 Moreover, siRNA-mediated knockdown of the CXCL8-target gene Bcl-2 increased the sensitivity of PC3 cells to 5-FU. Fluorouracil 108-112 C-X-C motif chemokine ligand 8 Homo sapiens 42-47 22715377-6 2012 A comparative transcriptomic analysis performed in HEK-293 cells expressing either wild-type HA-p65 or a non-phosphorylatable mutant HA-p65(S547A) identified several differentially transcribed genes after an etoposide treatment (e.g. IL8, A20, SELE). Etoposide 208-217 C-X-C motif chemokine ligand 8 Homo sapiens 234-237 22715377-9 2012 Cells expressing p65(S547A) have a higher level of histone H3 acetylated on Lys(9) at the IL8 promoter, which is in agreement with the higher gene induction observed. Lysine 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 22586462-2 2012 They consist of a conserved three-dimensional (3D) structure, so-called IL8-like chemokine fold, which is supported by disulfide bridges characteristic of this protein family. Disulfides 119-128 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 22396773-6 2012 Consistently, TPT-treated cells exhibit elevated expression of multiple cytokines such as IFN-beta, TNF-alpha, IL-6 and IL-8. Topotecan 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 22470478-9 2012 However, Que is more effective than cromolyn in inhibiting IL-8 and TNF release from LAD2 mast cells stimulated by SP. Quercetin 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 22470478-9 2012 However, Que is more effective than cromolyn in inhibiting IL-8 and TNF release from LAD2 mast cells stimulated by SP. Cromolyn Sodium 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 22363678-3 2012 We report here that next to the beta(2)-agonist fenoterol, direct and specific activation of either exchange protein directly activated by cAMP (Epac) or protein kinase A (PKA) reduced cigarette smoke extract (CSE)-induced IL-8 mRNA expression and protein release by human ASM cells. Cyclic AMP 139-143 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 22469636-10 2012 Interestingly, proinflammatory IL-8 was elevated in those subjects with evidence of AT and E compared to those with AT and NAD. nadide 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 22295067-10 2012 In terms of trans-repression, CpdA and ZK216348 effectively inhibited NF-kappaB activity and IL-8 secretion, but showed less trans-activation potency. CPDA 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 22295067-10 2012 In terms of trans-repression, CpdA and ZK216348 effectively inhibited NF-kappaB activity and IL-8 secretion, but showed less trans-activation potency. ZK 216348 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 22036725-11 2012 In addition, SM enhanced phosphorylation of NF-kB p65 and release of TNF-alpha, interleukin (IL)-6 and IL-8. Samarium 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 20665032-0 2012 Nicotine inhibits tumor necrosis factor-alpha induced IL-6 and IL-8 secretion in fibroblast-like synoviocytes from patients with rheumatoid arthritis. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 20665032-4 2012 Nicotine at concentrations of 0.1-10 muM dose reduced the protein and mRNA expression of IL-6 and IL-8 induced by tumor necrosis factor-alpha (TNFalpha). Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 23091851-8 2012 The CHD and MS patients who carried the Pro allele showed a significant metformin-induced reduction in weight, waist circumference, body mass index, and concentrations of TC, C-peptide, and cytokines, such IL-1beta, IL-6, IL-8, and TNF-alpha. Metformin 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 22015448-0 2012 Interleukin-8 (IL-8) over-production and autocrine cell activation are key factors in monomethylarsonous acid [MMA(III)]-induced malignant transformation of urothelial cells. monomethylarsonous acid 86-109 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 22289755-6 2012 Compared with the HSP serum group, the levels of IL-8, TNF-alpha, and NO in the HSP serum plus methylprednisolone group decreased significantly (P<0.05). Methylprednisolone 95-113 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 22015448-0 2012 Interleukin-8 (IL-8) over-production and autocrine cell activation are key factors in monomethylarsonous acid [MMA(III)]-induced malignant transformation of urothelial cells. monomethylarsonous acid 86-109 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 21798286-4 2011 However, HuMCs from the remaining donors and the LAD2 human MC line responded to PGE(2) and sulprostone with marked enhancement of antigen-mediated degranulation and IL-8 production in a similar manner to that observed in mouse BMMCs. Methylcholanthrene 11-13 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 21798286-4 2011 However, HuMCs from the remaining donors and the LAD2 human MC line responded to PGE(2) and sulprostone with marked enhancement of antigen-mediated degranulation and IL-8 production in a similar manner to that observed in mouse BMMCs. Prostaglandins E 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 21975045-0 2011 Influence of sodium fluoride (NaF) on the crystallization and spectral properties of L-tyrosine. Sodium Fluoride 13-28 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 21975045-0 2011 Influence of sodium fluoride (NaF) on the crystallization and spectral properties of L-tyrosine. Tyrosine 85-95 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 21975045-3 2011 L-Tyrosine has been crystallized in silica gel by double diffusion technique with and without the addition of NaF. Tyrosine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 21975045-9 2011 Optical band gap energy of NaF grown l-tyrosine crystallite is estimated as 4.28eV. Tyrosine 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 21877251-8 2011 Using oligonucleotide microarray, we demonstrated a dramatic increase in proinflammatory cytokine and chemokine transcripts (CXCL10, CXCL11, TNFSF10, CCL5, CCL4, CCL2, IFNB1, CCL20, IL-8, and CCL11). Oligonucleotides 6-21 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 22029665-5 2011 The effect of fluorine source on the optical properties of UCNPs was investigated by using NH(4)F, NH(4)HF(2), NaF, and 1-butyl-3-methylimidazolium tetrafluoroborate (BmimBF(4)) as different fluorine sources; NH(4)F proved to be the best one, making the luminescent intensity increase at least 2 orders of magnitude. Fluorine 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 21930886-5 2011 Rifampin significantly increased the secretion of interleukin 8 (IL-8) in both untreated cells (P < 0.001) and cytokine-treated cells (P < 0.006). Rifampin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 21930886-5 2011 Rifampin significantly increased the secretion of interleukin 8 (IL-8) in both untreated cells (P < 0.001) and cytokine-treated cells (P < 0.006). Rifampin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 25386288-6 2011 In addition, ellagic acid promoted G1 cell cycle arrest, increased levels of apoptosis and decreased synthesis of IL-1beta and IL-8 in melanoma cells. Ellagic Acid 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 21778813-4 2011 Because CXCL8 played an important role in neutrophil infiltration and activation, we performed the LMT and measured CXCL8 levels in patients with hypersensitivity to beta-lactam antibiotics (beta-lactams) and antipyretic analgesics (APAs) and investigated the pathogenic mechanism of hypersensitivity to these drugs. beta-Lactams 166-177 C-X-C motif chemokine ligand 8 Homo sapiens 8-13 21778813-7 2011 The CXCL8 concentrations were significantly higher in patients after beta-lactams administration (175.9 +- 71.2 ng/mL) than those without beta-lactams administration (48.3 +- 34.9 ng/mL). beta-Lactams 69-81 C-X-C motif chemokine ligand 8 Homo sapiens 4-9 21778813-7 2011 The CXCL8 concentrations were significantly higher in patients after beta-lactams administration (175.9 +- 71.2 ng/mL) than those without beta-lactams administration (48.3 +- 34.9 ng/mL). beta-Lactams 138-150 C-X-C motif chemokine ligand 8 Homo sapiens 4-9 21778813-9 2011 CONCLUSIONS: Increased CXCL8 levels produced by beta-lactams administration were accompanied by LMIA. beta-Lactams 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 23-28 21778813-10 2011 CXCL8 may be involved in LMIA and play a role in beta-lactam allergies. beta-Lactams 49-60 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 22829094-3 2011 AZD1480 at low doses (0.1-1 mu) potently inhibited STATs phosphorylation, but did not predictably result in antiproliferative effects, as it activated a negative-feedback loop causing phosphorylation of JAK2 and extracellular signal-regulated kinases 1 and 2 (ERK1/2), and increased IP-10, RANTES and interleukin (IL)-8 concentrations in the supernatants. AZD 1480 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 301-319 21996014-6 2011 A newly developed CS induced rat COPD model was employed to study time courses of IL-17 and IL-8 release and nucleated cell accumulation. Cesium 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 22092504-9 2011 RESULTS: Although Dex dose dependently inhibited IL-8 release induced by 5 ng/mL IL-13, Dex 0.001-1 mug/mL had no effect on IL-13 induced MUC5AC protein secretion or mRNA expression. Dexamethasone 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 21479633-7 2011 DHA significantly inhibited NF-kappaB DNA-binding activity, so as to tremendously decrease the expression of NF-kappaB-targeted proangiogenic gene products: VEGF, IL-8, COX-2, and MMP-9 in vitro. artenimol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 21996445-9 2011 DISCUSSION: Nickel ions from the Ni-Cr alloys permeated the epithelial cells and activated a proinflammatory response, namely IL-1a, IL-8 and PGE2 expression. Nickel 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 21963154-7 2011 Low levels of dityrosine cross-links were detected in copper/H2O2-treated IL-8 (CXCL8), which has one tyrosine residue, and none were detected in ENA-78 (CXCL5), which has none. dityrosine 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 21996445-9 2011 DISCUSSION: Nickel ions from the Ni-Cr alloys permeated the epithelial cells and activated a proinflammatory response, namely IL-1a, IL-8 and PGE2 expression. Chromium 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 21963154-7 2011 Low levels of dityrosine cross-links were detected in copper/H2O2-treated IL-8 (CXCL8), which has one tyrosine residue, and none were detected in ENA-78 (CXCL5), which has none. Copper 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 22031535-4 2011 LMW-HA-activated AFAP-110 then binds to filamentous actin (F-actin) resulting in MyD88/nuclear factor-kappaB (NF-kappaB) nuclear translocation, NF-kappaB-specific transcription, and target gene [interleukine 1beta and interleukine-8 (IL-1beta and IL-8)] expression. lmw-ha 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 21963154-7 2011 Low levels of dityrosine cross-links were detected in copper/H2O2-treated IL-8 (CXCL8), which has one tyrosine residue, and none were detected in ENA-78 (CXCL5), which has none. Hydrogen Peroxide 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 21995333-0 2011 Mast cell-derived TNF-alpha and histamine modify IL-6 and IL-8 expression and release from cutaneous tumor cells. Histamine 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 21963154-7 2011 Low levels of dityrosine cross-links were detected in copper/H2O2-treated IL-8 (CXCL8), which has one tyrosine residue, and none were detected in ENA-78 (CXCL5), which has none. Tyrosine 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 21964048-5 2011 The treatment of EPCs with TLR3 agonist Poly I:C up-regulated the expression of cytokines IL-1beta, IL-6, IL-8, TNF-alpha, IFN-alpha, and IFN-beta, indicating that EPCs expressed functional TLR3. Poly I 40-46 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 21930764-7 2011 Activation of the IL-8 promoter in transfected HEK293 cells was inhibited by manumycin A, BAY43-9006, U0126, and transfection with a dominant-negative Ras mutant. manumycin 77-88 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 21930764-7 2011 Activation of the IL-8 promoter in transfected HEK293 cells was inhibited by manumycin A, BAY43-9006, U0126, and transfection with a dominant-negative Ras mutant. Sorafenib 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 21964048-5 2011 The treatment of EPCs with TLR3 agonist Poly I:C up-regulated the expression of cytokines IL-1beta, IL-6, IL-8, TNF-alpha, IFN-alpha, and IFN-beta, indicating that EPCs expressed functional TLR3. Carbon 19-20 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 21930764-7 2011 Activation of the IL-8 promoter in transfected HEK293 cells was inhibited by manumycin A, BAY43-9006, U0126, and transfection with a dominant-negative Ras mutant. U 0126 102-107 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 21414766-5 2011 Nicotinamide treatment resulted in a significant reduction of basal and/or LPS-stimulated release and gene expression of the pro-inflammatory cytokines TNF-alpha, IL-6 and the chemokine IL-8, and the release of the prostaglandins PGE(2) and PGF(2)alpha and cyclooxygenase (COX)-2 mRNA expression. Niacinamide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 21956421-11 2011 When treated with TSH, thyroid fibroblasts generate IL-6 and IL-8. Thyrotropin 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 22125787-10 2011 The IC25 of IL-8 inhibition by dexamethasone was higher in nasal polyp than in nasal mucosa fibroblasts. Dexamethasone 31-44 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 21917909-5 2011 Corticosteroid (dexamethasone) sensitivity was determined on tumor necrosis factor-alpha (TNF-alpha)-induced interleukin (IL)-8 production. Dexamethasone 16-29 C-X-C motif chemokine ligand 8 Homo sapiens 109-127 21903370-8 2011 MKP-1 mRNA was increased and IL-8 mRNA was significantly inhibited by BUD800, SYM100 and SYM200 versus placebo. bud800 70-76 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 21824526-3 2011 Stimulation with TvSP induced up-regulation of IL-8 protein secretion in HMC-1 cells. tvsp 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 21824526-6 2011 Moreover, TvSP-induced IL-8 production and phosphorylation of NF-kappaB or CREB were inhibited when HMC-1 cells were stimulated with modified TvSP collected from 5-lipooxygenase inhibitor-treated trichomonads. tvsp 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 21824526-6 2011 Moreover, TvSP-induced IL-8 production and phosphorylation of NF-kappaB or CREB were inhibited when HMC-1 cells were stimulated with modified TvSP collected from 5-lipooxygenase inhibitor-treated trichomonads. tvsp 142-146 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 21824526-9 2011 Finally, TvSP-induced IL-8 production was inhibited by pretreatment with IkappaB or CREB inhibitors. tvsp 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 21964474-5 2011 Normalized IL-8 concentration for C60(OH)20 was not significantly different from control, while C60(OH)24 and C60(OH)32 showed a significant decrease at 24 and 48 h. These results suggest that different hydroxylation of fullerenes caused no cytotoxicity or inflammation up to 8.55 mug/ml. Fullerenes 220-230 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 22107692-8 2011 Citrate could significantly decrease systemic pre-filter serum MPO levels from baseline at 6 h (median 43.5 vs. 17.3 ng/mL, P<0.01) as well as IL-8 levels (P<0.05) whereas heparin provided only significant TNF-alpha reduction (P<0.05). Citric Acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 22107694-0 2011 Down-modulation of toll-like receptor 2 expression on granulocytes and suppression of interleukin-8 production due to in vitro treatment with cellulose acetate beads. acetylcellulose 142-159 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 22525504-7 2011 p38 MAPK inhibitor (SB203580) could significantly inhibit IL-8 production in a dose-dependent manners (F = 65.47, P < 0.01), and partially inhibited NF-kB p65 nuclear translocation in a dose-dependent manner (F=141.20, P < 0.05). SB 203580 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 22152804-4 2011 Furthermore, whether TLR4 inhibitor, TAK-242, could interrupt the expression of TRIF as well as some inflammatory cytokines such as IL-6, IL-8 and TNF-alpha in THP-1 cells stimulated with beta2 GPI/anti-beta2 GPI complex was also investigated. ethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylate 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 22019593-0 2011 Interactions of interleukin-8 with the human chemokine receptor CXCR1 in phospholipid bilayers by NMR spectroscopy. Phospholipids 73-85 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 22019593-8 2011 The interaction is tight enough to immobilize IL-8 along with the receptor in phospholipid bilayers and is specific enough to result in well-aligned samples in oriented sample solid-state NMR spectra. Phospholipids 78-90 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 21493783-0 2011 Steroid-insensitive ERK1/2 activity drives CXCL8 synthesis and neutrophilia by airway smooth muscle. Steroids 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 21925595-7 2011 Importantly, both severe (0.5% O(2)) and mild (5% O(2)) hypoxia diminished IL-8 expression despite the stabilization of both HIF-1 and HIF-2. o(2)) 31-36 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 21925595-7 2011 Importantly, both severe (0.5% O(2)) and mild (5% O(2)) hypoxia diminished IL-8 expression despite the stabilization of both HIF-1 and HIF-2. o(2) 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 21820074-13 2011 Humic acid also induces the release of IL-8 from human monocytes and enhances the CSE-induced IL-8 release. Humic Substances 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 21820074-13 2011 Humic acid also induces the release of IL-8 from human monocytes and enhances the CSE-induced IL-8 release. Humic Substances 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 21820074-15 2011 Moreover, humic acid promotes IL-8 release from human monocytes. Humic Substances 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 21840384-9 2011 Air followed by Asp exposure tended to induce IL-8 expression whereas IL-8 production tended to increase after FA and Asp exposure compared to FA and air exposure. Aspartic Acid 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 21840384-9 2011 Air followed by Asp exposure tended to induce IL-8 expression whereas IL-8 production tended to increase after FA and Asp exposure compared to FA and air exposure. Aspartic Acid 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 21493783-5 2011 In ex vivo ASMCs, TNF-alpha but not IL-17A induced expression of the neutrophil chemoattractant CXCL8. asmcs 11-16 C-X-C motif chemokine ligand 8 Homo sapiens 96-101 21925169-6 2011 PGE2 increased the second EGFR-P and IL-8 production via binding to its Gi-protein-coupled E-prostanoid (EP)3 receptor. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 22010965-8 2011 Furthermore, the basal cytokine profile (high IL-8, MIG, IP-10 and IL-4 levels and low IL-5, MIP1a, MIP1b, IL12/p70) was predictive of clinical response to lenalidomide. Lenalidomide 156-168 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 21946433-4 2011 Monosodium urate crystals were able to significantly increase the release of the inflammatory cytokine IL-6, the chemokine CXCL8 and the matrix metalloproteinase (MMP)-1 from both normal and RA-FLS (all P<0.05). Uric Acid 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 21946433-5 2011 Moreover, the additive or synergistic effect on the release of IL-6, CXCL8 and MMP-1 from both normal and RA-FLS was observed following the combined treatment with monosodium urate crystals and TNF-alpha or IL-1beta. Uric Acid 164-180 C-X-C motif chemokine ligand 8 Homo sapiens 69-74 21742513-0 2011 Autocrine production of interleukin-8 confers cisplatin and paclitaxel resistance in ovarian cancer cells. Cisplatin 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 21742513-0 2011 Autocrine production of interleukin-8 confers cisplatin and paclitaxel resistance in ovarian cancer cells. Paclitaxel 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 21925169-8 2011 Thus, we conclude that a positive feedback pathway involving COX-2/PGE2/EP3 receptor-dependent EGFR reactivation exaggerates IL-8 production in NCI-H292 cancer cells but not in NHBE (normal) cells. Dinoprostone 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 21785859-6 2011 In addition, cysteine and histidine significantly inhibited the expression of ICAM-1 and production of IL-8 in THP-1 cells and PBMCs. Cysteine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 21785859-6 2011 In addition, cysteine and histidine significantly inhibited the expression of ICAM-1 and production of IL-8 in THP-1 cells and PBMCs. Histidine 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 22000456-6 2011 Resveratrol enhanced LPS- and heat stress-induced expression of HO-1 and hBD-2 but reduced IL-8 messenger RNA levels. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 22086795-7 2011 RESULTS: Among 12 cytokines, IL-6, IL-8, IL-10, and TNF-alpha were significantly elevated in patients with resistance against lamivudine compared with patients maintaining response. Lamivudine 126-136 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 21865591-8 2011 Furthermore, synthetic ghrelin inhibited the production of IL-8 from TNF-alpha or LPS-stimulated oral epithelial cells. Ghrelin 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 21716324-5 2011 Bafilomycin A1, which inhibits endosomal acidification to block the TLR3 pathway, blocked the dsRNA-induced expression of TSLP, IL-8, IFN-beta, and other molecules including the dsRNA sensors, whereas it did not inhibit diacyllipopeptide-induced expression of TSLP and IL-8. bafilomycin A1 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 21716324-5 2011 Bafilomycin A1, which inhibits endosomal acidification to block the TLR3 pathway, blocked the dsRNA-induced expression of TSLP, IL-8, IFN-beta, and other molecules including the dsRNA sensors, whereas it did not inhibit diacyllipopeptide-induced expression of TSLP and IL-8. bafilomycin A1 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 269-273 21796149-3 2011 beta-Glucan stimulation significantly increased IL-8, IL-6, and IL-1alpha production by NHEKs. beta-Glucans 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 21796149-4 2011 Well-differentiated NHEKs produced elevated IL-8 levels, whereas ATP, a danger signal, significantly increased IL-8 and IL-6 production, and the pathogen-associated compound, poly(I:C), augmented IL-1alpha production by beta-glucan-stimulated NHEKs. Adenosine Triphosphate 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 21796149-10 2011 Treatment with the ERK inhibitor PD98059 and with the p38 kinase inhibitor SB203580 effectively suppressed beta-glucan-induced IL-8 production by NHEKs. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 21796149-10 2011 Treatment with the ERK inhibitor PD98059 and with the p38 kinase inhibitor SB203580 effectively suppressed beta-glucan-induced IL-8 production by NHEKs. SB 203580 75-83 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 21796149-10 2011 Treatment with the ERK inhibitor PD98059 and with the p38 kinase inhibitor SB203580 effectively suppressed beta-glucan-induced IL-8 production by NHEKs. beta-Glucans 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 21417583-4 2011 Therefore, we investigated the effects of AZM on IL-8 production in an oral epithelial cell line. Azithromycin 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 21417583-8 2011 RESULTS: IL-8 mRNA expression, IL-8 production, and NF-kappaB activation in LPS-stimulated KB cells were inhibited by the addition of AZM. Azithromycin 134-137 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 21417583-8 2011 RESULTS: IL-8 mRNA expression, IL-8 production, and NF-kappaB activation in LPS-stimulated KB cells were inhibited by the addition of AZM. Azithromycin 134-137 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 21417583-10 2011 CONCLUSIONS: This study suggests that AZM inhibits LPS-induced IL-8 production in an oral epithelial cell line, in part caused by the suppression of Rac1 and NF-kappaB activation. Azithromycin 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 21842098-4 2011 The results obtained demonstrated that zinc, nickel and cadmium significantly activate NF-kappaB, and the release of the chemokine IL-8. Nickel 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 21842098-4 2011 The results obtained demonstrated that zinc, nickel and cadmium significantly activate NF-kappaB, and the release of the chemokine IL-8. Cadmium 56-63 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 22292182-46 2011 CONCLUSION: Hyperoxia induced intracellular ROS production can up-regulate TLR2/4 expression in A549 cells, leading to the release pro-inflammatory cytokines IL-6 and IL-8 from these cells. Reactive Oxygen Species 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 21992677-0 2011 Parthenolide inhibits ERK and AP-1 which are dysregulated and contribute to excessive IL-8 expression and secretion in cystic fibrosis cells. parthenolide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 21936573-2 2011 Crude MRPs derived from Glu-Lys showed the greatest capacity (P < 0.05) to inhibit nitric oxide (NO) and interleukin 8 (IL-8) production in interferon gamma and phorbol ester-induced Caco-2 cells. Glucose 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 21936573-2 2011 Crude MRPs derived from Glu-Lys showed the greatest capacity (P < 0.05) to inhibit nitric oxide (NO) and interleukin 8 (IL-8) production in interferon gamma and phorbol ester-induced Caco-2 cells. Glucose 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 21936573-2 2011 Crude MRPs derived from Glu-Lys showed the greatest capacity (P < 0.05) to inhibit nitric oxide (NO) and interleukin 8 (IL-8) production in interferon gamma and phorbol ester-induced Caco-2 cells. Lysine 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 21936573-2 2011 Crude MRPs derived from Glu-Lys showed the greatest capacity (P < 0.05) to inhibit nitric oxide (NO) and interleukin 8 (IL-8) production in interferon gamma and phorbol ester-induced Caco-2 cells. Lysine 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 21936573-2 2011 Crude MRPs derived from Glu-Lys showed the greatest capacity (P < 0.05) to inhibit nitric oxide (NO) and interleukin 8 (IL-8) production in interferon gamma and phorbol ester-induced Caco-2 cells. Phorbol Esters 164-177 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 21936573-2 2011 Crude MRPs derived from Glu-Lys showed the greatest capacity (P < 0.05) to inhibit nitric oxide (NO) and interleukin 8 (IL-8) production in interferon gamma and phorbol ester-induced Caco-2 cells. Phorbol Esters 164-177 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 21992677-11 2011 Since we previously showed that parthenolide inhibits excessive IL-8 production by CF cells, we evaluated its effects on MAPK and AP-1 activation and showed that parthenolide inhibited ERK and AP-1 activation. parthenolide 32-44 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 21992677-11 2011 Since we previously showed that parthenolide inhibits excessive IL-8 production by CF cells, we evaluated its effects on MAPK and AP-1 activation and showed that parthenolide inhibited ERK and AP-1 activation. parthenolide 162-174 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 21992677-12 2011 Using a luciferase promoter assay, our studies showed that parthenolide decreased activation of the IL-8 promoter in CF cells stimulated with TNFalpha/IL-1beta. parthenolide 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 21992677-14 2011 Parthenolide inhibited both NFkappaB and MAPK/AP-1 pathways contributing to the inhibition of IL-8 production. parthenolide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 21989944-0 2011 Low molecular weight hyaluronan, via AP-1 and NF-kappaB signalling, induces IL-8 in transformed bronchial epithelial cells. Hyaluronic Acid 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 21925143-4 2011 Treatment of Ca9-22 cells and HOK with oxLDL induced an up-regulation of IL-8 and the PGE(2)-producing enzymes, cyclooxygenase-2 and microsomal PGE(2) synthase-1. oxldl 39-44 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 21989944-2 2011 In addition, high tidal volume mechanical ventilation has been shown to increase IL-8 production in a mechanism mediated, at least in part, by low molecular weight hyaluronan (LWM-HA). Hyaluronic Acid 164-174 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21989944-2 2011 In addition, high tidal volume mechanical ventilation has been shown to increase IL-8 production in a mechanism mediated, at least in part, by low molecular weight hyaluronan (LWM-HA). lwm-ha 176-182 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21989944-7 2011 The inhibition of JNK, ERK1/2 and NF-kappaB blocked IL-8 secretion in response to LMW-HA. lmw-ha 82-88 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 21989944-8 2011 CONCLUSION: The data suggest that LMW-HA produced by lung fibroblasts in response to cyclic stretch increases the secretion of IL-8 in transformed bronchial epithelial cells via AP-1 and NF-kappaB signalling pathways. lmw-ha 34-40 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 21844189-7 2011 Aspirin was hydrolyzed by HEK cells transfected with PAFAH1B2 or PAFAH1B3, and the competitive type I PAF acetylhydrolase inhibitor NaF reduced erythrocyte hydrolysis of aspirin. Aspirin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 132-135 21844189-7 2011 Aspirin was hydrolyzed by HEK cells transfected with PAFAH1B2 or PAFAH1B3, and the competitive type I PAF acetylhydrolase inhibitor NaF reduced erythrocyte hydrolysis of aspirin. Aspirin 170-177 C-X-C motif chemokine ligand 8 Homo sapiens 132-135 21782151-7 2011 RESULTS: Before the administration of the drugs, aqueous levels of IL-8, IP-10, MCP-1, and VEGF were significantly higher in the DME group than in the control group. dme 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 21919510-4 2011 The introduction of NaF into the solution combustion synthesis (SCS), which is a generally adopted synthetic route for mass productions of various oxide nanoparticles, results in better particle dispersity and a drastic increase in specific surface area compared to the conventional SCS. Oxides 147-152 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 21693690-6 2011 Stimulation of NOD1 with a synthetic ligand Tri-DAP induces proinflammatory chemokine MCP-1, RANTES, and cytokine TNF-alpha and MIP-2 (human IL-8 homolog) and IL-6 mRNA expression in 3T3-L1 adipocytes in a time- and dose-dependent manner. L-Ala-gamma-D-Glu-meso-diaminopimelic acid 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21297080-0 2011 Hydrogen sulfide inhibits proliferation and release of IL-8 from human airway smooth muscle cells. Hydrogen Sulfide 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 21297080-6 2011 Exposure of ASM to H(2)S "donors" inhibited this proliferation and IL-8 release. h(2) 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 21297080-9 2011 Inhibition of CBS, but not cystathionine-gamma-lyase, reversed the inhibitory effect of H(2)S on proliferation and IL-8 release, indicating that this is dependent on CBS. Hydrogen Sulfide 88-93 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 21297080-11 2011 Finally, we found that exogenous H(2)S inhibited the phosphorylation of extracellular signal-regulated kinase-1/2 and p38, which could represent a mechanism by which H(2)S inhibited cellular proliferation and IL-8 release. Hydrogen Sulfide 33-38 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 22103940-5 2011 In addition, skin irritation induced by an application of sodium dodecyl sulphate resulted in significantly higher lactate dehydrogenase leakage, and interleukin (IL)-6 and IL-8 levels, than in the control model. Sodium Dodecyl Sulfate 58-81 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 21297080-11 2011 Finally, we found that exogenous H(2)S inhibited the phosphorylation of extracellular signal-regulated kinase-1/2 and p38, which could represent a mechanism by which H(2)S inhibited cellular proliferation and IL-8 release. Hydrogen Sulfide 166-171 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 21707494-3 2011 Since the old anti-Hansen"s disease drug dapsone inhibits neutrophil migration along an IL-8 gradient towards increasing concentrations, and is used therapeutically for this attribute to good effect in dermatitis herpetiformis, bullous pemphigoid and rheumatoid arthritis, we suggest dapsone may deprive glioblastoma of neutrophil-mediated growth promoting effects. Dapsone 41-48 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 21297080-12 2011 In summary, H(2)S production provides a novel mechanism for regulation of ASM proliferation and IL-8 release. Hydrogen Sulfide 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 21734258-8 2011 RLN suppression of CSF2 and IL8 was sensitive to the GR-antagonist mifepristone (RU-486). Mifepristone 67-79 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 21734258-8 2011 RLN suppression of CSF2 and IL8 was sensitive to the GR-antagonist mifepristone (RU-486). Mifepristone 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 21771721-5 2011 12-O-tetradecanoylphorbol 13-acetate-induced differentiation of human U937 monocytes increased the expression and secretion of inflammatory cytokines such as tumor necrosis factor alpha, interleukin (IL)-6 and IL-8. Tetradecanoylphorbol Acetate 0-36 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 21688034-7 2011 Erlotinib suppressed the production of osteolytic factors, such as parathyroid hormone-related protein (PTHrP), IL-8, IL-11 and vascular endothelial growth factor (VEGF) in NCI-H292 cells. Erlotinib Hydrochloride 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 21724580-6 2011 In the vitamin D(3) supplementation group, TNF-alpha decreased 13%, IL-6 32%, IL-1beta 50%, and IL-8 15%; in the calcium supplementation group, IL-6 decreased 37%, IL-8 11%, and IL-1beta 27%. Vitamin D 7-16 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 21436242-0 2011 Dapsone inhibits IL-8 secretion from human bronchial epithelial cells stimulated with lipopolysaccharide and resolves airway inflammation in the ferret. Dapsone 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 21665565-3 2011 METHODS: We studied IL-8 expression and regulatory signaling pathways in cultured HAECs exposed to Mexicali PM suspended in media for 0-4 hr. mexicali pm 99-110 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 21806984-10 2011 Finally, exposure of human colon biopsies from inflammatory bowel diseases patients to rifaximin reduced mRNA levels of IL-8, Rantes, MIP-3alpha and TNFalpha induced by LPS. Rifaximin 87-96 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 21720792-8 2011 In addition, the serum levels of IFN-gamma and Cort were significantly higher and IL-8 levels were lower in CABP when compared to pyelonephritis or urosepsis. 2-CARBOXYARABINITOL-1,5-DIPHOSPHATE 108-112 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 21793939-6 2011 Association of Adapalene and BPO significantly decreased expression of Ki67, alpha(2) and alpha(6) integrins, TLR-2, beta-defensin 4 and IL-8 in inflammatory acne skin, whereas single treatments with Adapalene or BPO alone were less effective. Adapalene 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 21793939-6 2011 Association of Adapalene and BPO significantly decreased expression of Ki67, alpha(2) and alpha(6) integrins, TLR-2, beta-defensin 4 and IL-8 in inflammatory acne skin, whereas single treatments with Adapalene or BPO alone were less effective. Benzoyl Peroxide 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 20845069-0 2011 Synergistic effect of tumor necrosis factor-alpha and hydrogen peroxide on the induction of IL-8 production in human intestinal Caco-2 cells. Hydrogen Peroxide 54-71 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21762685-0 2011 Anti-inflammatory effects of garenoxacin on IL-8 production and ERK1/2 activation induced by lipopolysaccharides in A549 and THP-1 cells. garenoxacin 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 21777689-0 2011 Safrole oxide induces human umbilical vein endothelial cell transdifferentiation to 5-hydroxytryptaminergic neuron-like cells through tropomyosin receptor kinase A/cyclooxygenase 2/nuclear factor-kappa B/interleukin 8 signaling. safrole oxide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 204-217 21777689-5 2011 Safrole oxide elevated the levels of cyclooxygenase 2 (COX-2), interleukin-8 (IL-8) and reactive oxygen species (ROS), which was accompanied by nuclear factor-kappa B (NF-kappaB) nuclear translocation during the transdifferentiation. safrole oxide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 21934447-8 2011 The poly (inosinic acid:cytidylic acid)-mediated lactic acid effect on IL-1beta and IL-8 release was abrogated when the lactic acid was neutralized or if acetic acid was substituted for lactic acid. Poly I 4-23 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21777689-5 2011 Safrole oxide elevated the levels of cyclooxygenase 2 (COX-2), interleukin-8 (IL-8) and reactive oxygen species (ROS), which was accompanied by nuclear factor-kappa B (NF-kappaB) nuclear translocation during the transdifferentiation. safrole oxide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 21777689-9 2011 During this process, the increased levels of COX-2/IL-8 and the subsequent elevation of ROS production induced NF-kappaB nuclear translocation and IL-8 secretion. Reactive Oxygen Species 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 21744278-5 2011 SP600125 attenuated t10,c12 CLA-mediated induction of inflammatory genes, including interleukin (IL)-6, IL-8, IL-1beta, ATF3, monocyte chemoattractant protein (MCP)-1, and cyclooxygenase-2. pyrazolanthrone 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 21744278-6 2011 Consistent with these data, SP600125 prevented t10,c12 CLA-mediated secretion of IL-8, IL-6, and MCP-1. pyrazolanthrone 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21934447-6 2011 Poly (inosinic acid:cytidylic acid) by itself stimulated the release of IL-6 (305 pg/mL) and enhanced IL-8 production (2.8 ng/mL). Poly I 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21934447-6 2011 Poly (inosinic acid:cytidylic acid) by itself stimulated the release of IL-6 (305 pg/mL) and enhanced IL-8 production (2.8 ng/mL). Cytidine Monophosphate 20-34 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21934447-8 2011 The poly (inosinic acid:cytidylic acid)-mediated lactic acid effect on IL-1beta and IL-8 release was abrogated when the lactic acid was neutralized or if acetic acid was substituted for lactic acid. Cytidine Monophosphate 24-39 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21934447-7 2011 The combination of poly (inosinic acid:cytidylic acid) and lactic acid markedly increased IL-8 production (5.0 ng/mL) and induced the release of IL-1beta (96.2 pg/mL). Poly I 19-38 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 21934447-7 2011 The combination of poly (inosinic acid:cytidylic acid) and lactic acid markedly increased IL-8 production (5.0 ng/mL) and induced the release of IL-1beta (96.2 pg/mL). Cytidine Monophosphate 39-53 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 21934447-8 2011 The poly (inosinic acid:cytidylic acid)-mediated lactic acid effect on IL-1beta and IL-8 release was abrogated when the lactic acid was neutralized or if acetic acid was substituted for lactic acid. Lactic Acid 49-60 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21934447-7 2011 The combination of poly (inosinic acid:cytidylic acid) and lactic acid markedly increased IL-8 production (5.0 ng/mL) and induced the release of IL-1beta (96.2 pg/mL). Lactic Acid 59-70 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 21934447-8 2011 The poly (inosinic acid:cytidylic acid)-mediated lactic acid effect on IL-1beta and IL-8 release was abrogated when the lactic acid was neutralized or if acetic acid was substituted for lactic acid. Lactic Acid 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21934447-8 2011 The poly (inosinic acid:cytidylic acid)-mediated lactic acid effect on IL-1beta and IL-8 release was abrogated when the lactic acid was neutralized or if acetic acid was substituted for lactic acid. Acetic Acid 154-165 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21934447-8 2011 The poly (inosinic acid:cytidylic acid)-mediated lactic acid effect on IL-1beta and IL-8 release was abrogated when the lactic acid was neutralized or if acetic acid was substituted for lactic acid. Lactic Acid 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 27156875-4 2011 Fluorine-18-Sodium Fluoride (18F-NaF) positron emission tomography/computed tomography (PET/CT) imaging allows detection and quantification of arterial molecular calcification in heart and across multiple vessels. fluorine-18-sodium fluoride 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 21587103-10 2011 RESULTS: In vitro, resveratrol exhibited an anti-inflammatory and anticatabolic effect on the messenger RNA and protein level for IL-6, IL-8, MMP1, MMP3 and MMP13. Resveratrol 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 21514398-9 2011 Compared to placebo Bimosiamose reduced the numbers of sputum neutrophils by 40% (p = 0.068) and concentrations of interleukin-8 and matrix-metalloproteinase-9 in sputum supernatant by 35% (p = 0.004) and 46% (p = 0.022), respectively. bimosiamose 20-31 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 21821700-8 2011 Significant reduction of IL-8 levels (P < 0.05) was seen in post-curcumin samples from patients with dental caries. Curcumin 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 22321839-6 2011 And Group B at post-operation was lower than Group C ((147 +- 19) vs (212 +- 18), P < 0.05); the pre-operative concentration of IL-8 was lowest in Group A ((85 +- 16) ng/L vs (151 +- 18) ng/L & (164 +- 22) ng/L, P < 0.05). Adenosine Monophosphate 196-199 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 22321839-8 2011 There were significantly positive correlations between depression scores, the expression of CD(40) and the plasma concentration of IL-8. Cadmium 92-94 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 21669195-3 2011 It was anticipated that PGP exerts its chemoatactic activity by mimicking key sequences found within classical neutrophil chemokines, such as CXCL8, and binding their receptors, CXCR1/2. prolyl-glycyl-proline 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 142-147 21821055-0 2011 Dimethyl sulphoxide and dimethyl sulphone are potent inhibitors of IL-6 and IL-8 expression in the human chondrocyte cell line C-28/I2. Dimethyl Sulfoxide 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 21821055-0 2011 Dimethyl sulphoxide and dimethyl sulphone are potent inhibitors of IL-6 and IL-8 expression in the human chondrocyte cell line C-28/I2. dimethyl sulfone 24-41 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 21821055-8 2011 Long-term exposure of cells to DMSO (1%) or DMS (100mM) led to a dramatic downregulation of IL-6 and IL-8 expression which was accompanied by the deactivation of ERK1/2. Dimethyl Sulfoxide 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 21821055-8 2011 Long-term exposure of cells to DMSO (1%) or DMS (100mM) led to a dramatic downregulation of IL-6 and IL-8 expression which was accompanied by the deactivation of ERK1/2. dimethyl sulfone 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 21821055-10 2011 SIGNIFICANCE: In this study, we demonstrate that both DMSO and DMS represent strong anti-inflammatory properties by blocking constitutive as well as IL-1beta-induced IL-6 and IL-8 expression in the human chondrocyte cell line C-28/I2. Dimethyl Sulfoxide 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 21821055-10 2011 SIGNIFICANCE: In this study, we demonstrate that both DMSO and DMS represent strong anti-inflammatory properties by blocking constitutive as well as IL-1beta-induced IL-6 and IL-8 expression in the human chondrocyte cell line C-28/I2. dimethyl sulfone 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 21821700-9 2011 Although there was reduced IL-8 expression in 8 of 21 post-curcumin samples of HNSCC patients, the data did not reach statistical significance. Curcumin 59-67 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 21670067-5 2011 Nonreduced mCRP was largely inert in activating human coronary artery endothelial cells (HCAECs), whereas reduced or cysteine-mutated mCRP evoked marked release of IL-8 and monocyte chemoattractant protein-1 from HCAECs, with ~50% increase at a concentration of 1 mug/ml. Cysteine 117-125 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 21708216-3 2011 This study was undertaken to determine whether sodium fluoride (NaF) induces apoptosis in human oral cells and if so, whether Bad protein is involved in the process. Sodium Fluoride 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 21684332-5 2011 Here we demonstrate that CS induces the release of CXCL-8 and IL-1beta from human bronchial epithelial cells (HBE-14o). Cesium 25-27 C-X-C motif chemokine ligand 8 Homo sapiens 51-57 21684332-6 2011 CS-induced CXCL-8 production was inhibited by an antibody against TLR4 and by inhibitory ODN suggesting the involvement of TLR4 and TLR9. Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 11-17 21800892-9 2011 Both undigested and digested PPP3 significantly reduced IL-8 secretion in H(2)O(2)-induced Caco-2 cells, indicating that antioxidative stress bioactivity is retained upon digestion. Hydrogen Peroxide 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 21827134-4 2011 along with gonytolides B and C. Gonytolide A also increased TNF-alpha-stimulated production of IL-8 in human umbilical vein endothelial cells. gonytolide A 32-44 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 21862816-3 2011 CONCLUSION: Skeletal imaging with (18)F-NaF harnesses both the superior imaging characteristics of PET and the improved biodistribution of the fluoride tracer in comparison with standard nuclear techniques, resulting in excellent-quality images that can effectively be used to investigate the cause of bone pain in children. Fluorides 143-151 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 21684332-9 2011 The molecular mechanism of the CS-induced CXCL-8 production by the epithelial cells was further investigated. Cesium 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 42-48 21684332-11 2011 Interestingly, the inflammasome activator monosodium urate crystals (MSU) induced the release of CXCL-8 and IL-1beta and the caspase-1 inhibitor Z-VADDCB suppressed the CS-induced release of CXCL-8. SODIUM URATE 42-67 C-X-C motif chemokine ligand 8 Homo sapiens 97-103 21684332-11 2011 Interestingly, the inflammasome activator monosodium urate crystals (MSU) induced the release of CXCL-8 and IL-1beta and the caspase-1 inhibitor Z-VADDCB suppressed the CS-induced release of CXCL-8. SODIUM URATE 42-67 C-X-C motif chemokine ligand 8 Homo sapiens 191-197 21684332-11 2011 Interestingly, the inflammasome activator monosodium urate crystals (MSU) induced the release of CXCL-8 and IL-1beta and the caspase-1 inhibitor Z-VADDCB suppressed the CS-induced release of CXCL-8. msu 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 97-103 21684332-11 2011 Interestingly, the inflammasome activator monosodium urate crystals (MSU) induced the release of CXCL-8 and IL-1beta and the caspase-1 inhibitor Z-VADDCB suppressed the CS-induced release of CXCL-8. msu 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 191-197 21684332-11 2011 Interestingly, the inflammasome activator monosodium urate crystals (MSU) induced the release of CXCL-8 and IL-1beta and the caspase-1 inhibitor Z-VADDCB suppressed the CS-induced release of CXCL-8. z-VAD-DCB 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 191-197 21684332-11 2011 Interestingly, the inflammasome activator monosodium urate crystals (MSU) induced the release of CXCL-8 and IL-1beta and the caspase-1 inhibitor Z-VADDCB suppressed the CS-induced release of CXCL-8. Cesium 169-171 C-X-C motif chemokine ligand 8 Homo sapiens 191-197 21684332-13 2011 In conclusion, our results demonstrate that CS releases CXCL-8 from HBE-14o cells via TLR4 and TLR9 and inflammasome activation. Cesium 44-46 C-X-C motif chemokine ligand 8 Homo sapiens 56-62 21679760-6 2011 RESULTS: Sinomenine was found to significantly inhibit TNF-alpha induced cell surface expression of vascular cell adhesion molecule (VCAM)-1 and release of inflammatory cytokine and chemokine IL-6, CCL2 and CXCL8 from both normal and RA-FLS (all p<0.05). sinomenine 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 207-212 21571356-10 2011 L-glutathione reduced improved the downregulatory effects of FP on IKKalpha and IL-8 levels. Glutathione 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 21142820-5 2011 Apigenin significantly inhibits the inductive effect of phorbol 12-myristate 13-acetate (PMA) plus A23187 on the production of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-8, IL-6, and granulocyte-macrophage colony-stimulating factor (GM-CSF). Tetradecanoylphorbol Acetate 56-87 C-X-C motif chemokine ligand 8 Homo sapiens 193-211 21142820-5 2011 Apigenin significantly inhibits the inductive effect of phorbol 12-myristate 13-acetate (PMA) plus A23187 on the production of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-8, IL-6, and granulocyte-macrophage colony-stimulating factor (GM-CSF). Calcimycin 99-105 C-X-C motif chemokine ligand 8 Homo sapiens 193-211 21660963-8 2011 SB-328437 also diminished neutrophil recruitment in alveolar airspaces and improved LPS-induced ALI and production of IL-8 in bronchoalveolar lavage fluid. SB 328437 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 22072831-6 2011 Moreover, TvSP-induced IL-8 production was also significantly inhibited by pretreatment of neutrophils with ikappaB inhibitor or CREB inhibitor. tvsp 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 21056929-6 2011 Both genistein and E(2) inhibited basal and cAMP-induced mRNA levels of endogenous estrogen responsive genes containing CRE/CRE-like elements in their promoter regions, including interleukin (IL) 8 and serum- and glucocorticoid-inducible kinase 1 (SGK1). Genistein 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 179-197 21056929-6 2011 Both genistein and E(2) inhibited basal and cAMP-induced mRNA levels of endogenous estrogen responsive genes containing CRE/CRE-like elements in their promoter regions, including interleukin (IL) 8 and serum- and glucocorticoid-inducible kinase 1 (SGK1). Estradiol 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 179-197 21056929-6 2011 Both genistein and E(2) inhibited basal and cAMP-induced mRNA levels of endogenous estrogen responsive genes containing CRE/CRE-like elements in their promoter regions, including interleukin (IL) 8 and serum- and glucocorticoid-inducible kinase 1 (SGK1). Cyclic AMP 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 179-197 21056929-7 2011 Daidzein inhibited basal and cAMP-induced IL-8, but not SGK1 mRNA expression. daidzein 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 21056929-7 2011 Daidzein inhibited basal and cAMP-induced IL-8, but not SGK1 mRNA expression. Cyclic AMP 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 21976205-5 2011 An increase of IL-8 release could be determined at trichloramine concentrations higher than 10 mg/m(3) and an increase of IL-6 release at concentrations of 20 mg/m(3). nitrogen chloride 51-64 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 21777978-0 2011 Arsenic increases lipopolysaccharide-dependent expression of interleukin-8 gene by stimulating a redox-sensitive pathway that strengthens p38-kinase activation. Arsenic 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 21670847-9 2011 Our findings demonstrate an unequivocal role for MACs in angiogenesis, which is linked to paracrine release of cytokines such as IL-8. macs 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 21777978-7 2011 ATO increases LPS-dependent expression of IL-8 by enhancing p38-kinase activity induced by LPS in U937 cells. Arsenic Trioxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 21777978-4 2011 In the present study, we determined molecular basis of arsenic trioxide (ATO) effects on LPS-dependent expression of interleukin-8 (IL-8) gene in human monocytic cells. Arsenic Trioxide 55-71 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 21777978-10 2011 In addition, it markedly prevents the increase of both p38-kinase phosphorylation and IL-8 gene expression in LPS-stimulated cells pre-treated with ATO. Arsenic Trioxide 148-151 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 21777978-4 2011 In the present study, we determined molecular basis of arsenic trioxide (ATO) effects on LPS-dependent expression of interleukin-8 (IL-8) gene in human monocytic cells. Arsenic Trioxide 55-71 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 21777978-11 2011 Finally, as observed with the metalloid, pre-treatment of U937 cells with hydrogen peroxide markedly increases LPS-dependent expression of IL-8 gene. Hydrogen Peroxide 74-91 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 21777978-12 2011 In conclusion, our study demonstrates that ATO increases LPS-dependent expression of the inflammatory IL-8 gene by strengthening the p38 kinase activity induced by LPS through stimulation of a ROS/Src kinase signalling pathway. Arsenic Trioxide 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21777978-4 2011 In the present study, we determined molecular basis of arsenic trioxide (ATO) effects on LPS-dependent expression of interleukin-8 (IL-8) gene in human monocytic cells. Arsenic Trioxide 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 21777978-12 2011 In conclusion, our study demonstrates that ATO increases LPS-dependent expression of the inflammatory IL-8 gene by strengthening the p38 kinase activity induced by LPS through stimulation of a ROS/Src kinase signalling pathway. Reactive Oxygen Species 193-196 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21777978-4 2011 In the present study, we determined molecular basis of arsenic trioxide (ATO) effects on LPS-dependent expression of interleukin-8 (IL-8) gene in human monocytic cells. Arsenic Trioxide 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 21777978-5 2011 Pre-treatment with non cytotoxic concentrations of ATO for 48h increase IL-8 gene expression induced by LPS in monocytic U937 cells and in some, but not all, primary cultures of blood monocytes. Arsenic Trioxide 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 21777978-6 2011 Actinomycin D blocks induction of IL-8 mRNA levels in LPS-stimulated U937 cells pre-treated or not with ATO, which suggests that the metalloid strengthens LPS-dependent transcriptional regulation of IL-8 expression. Dactinomycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 21777978-6 2011 Actinomycin D blocks induction of IL-8 mRNA levels in LPS-stimulated U937 cells pre-treated or not with ATO, which suggests that the metalloid strengthens LPS-dependent transcriptional regulation of IL-8 expression. Dactinomycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 21637924-0 2011 Tetramethylpyrazine inhibits migration of SKOV3 human ovarian carcinoma cells and decreases the expression of interleukin-8 via the ERK1/2, p38 and AP-1 signaling pathways. tetramethylpyrazine 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 21471847-0 2011 Interleukin-8 overexpression in astrocytomas is induced by prostaglandin E2 and is associated with the transcription factors CCAAT/enhancer-binding protein-beta and CCAAT/enhancer-binding homologous protein. Dinoprostone 59-75 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 214-230 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 214-230 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 214-230 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 232-236 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 232-236 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 232-236 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 346-350 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 346-350 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-2 2011 OBJECTIVE: To evaluate (1) the correlation between the mRNA levels of IL-8, mPGES-1, and the main transcription factors (TFs) activating the IL-8 promoter in human brain tumors of different grades; (2) the role of prostaglandin E2 (PGE2) on IL-8 activation and the expression of these TFs in tumor-derived cells; and (3) the biological impact of PGE2 treatment and mPGES-1 silencing on IL-8 synthesis and tumorigenesis. Dinoprostone 346-350 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 21471847-6 2011 PGE2-treated astroglioma cells showed a marked upregulation of IL-8, C/EBP-beta, and CHOP, as well as increased proliferation and decreased apoptosis compared with untreated cells. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 21637924-5 2011 The role of TMP in association with IL-8 in the tumor cell migratory process remains unclear. tetramethylpyrazine 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 21637924-6 2011 The purpose of the present study was to determine whether TMP influences the migratory ability of a human ovarian carcinoma cell line (SKOV3) via regulation of IL-8 expression in vitro. tetramethylpyrazine 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 21471847-9 2011 CONCLUSION: (1) PGE2 is responsible for IL-8 overexpression, independently of the malignancy grade, in astrogliomas only. Dinoprostone 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 21637924-7 2011 Cell counts showed that treatment of SKOV3 with TMP (25-100 microg/ml) for 24 h did not decrease cell numbers, while an effect of TMP on the down-regulation of the expression of IL-8 was observed. tetramethylpyrazine 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 21471847-10 2011 (2) C/EBP-beta and CHOP may be involved in mediating PGE2-induced IL-8 activation in these tumors. Dinoprostone 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 21637924-8 2011 In addition, migration of SKOV3 cells was suppressed after treatment with TMP (25-100 microg/ml) for 24 h. Therefore, expression of IL-8 by SKOV3 cells correlates with their metastatic potential. tetramethylpyrazine 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 21637924-10 2011 Furthermore, IL-8 mRNA expression was inhibited significantly after co-incubation with PD98059 (ERK inhibitor) and SB203580 (p38 inhibitor), respectively. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 87-94 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 21637924-10 2011 Furthermore, IL-8 mRNA expression was inhibited significantly after co-incubation with PD98059 (ERK inhibitor) and SB203580 (p38 inhibitor), respectively. SB 203580 115-123 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 21637924-12 2011 Our data suggest that TMP may inhibit tumor cell invasion and migration, at least in part, through its down-regulation of IL-8 expression. tetramethylpyrazine 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 24900265-0 2011 Aryltriflates as a Neglected Moiety in Medicinal Chemistry: A Case Study from a Lead Optimization of CXCL8 Inhibitors. aryltriflates 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 21623862-4 2011 DA-6034 significantly inhibited NF-kappaB activation and upregulated the expressions of interleukin-8 (IL-8) and monocyte chemoattractant protein-1 in MKN-45 cells infected with H. pylori. recoflavone 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 21623862-4 2011 DA-6034 significantly inhibited NF-kappaB activation and upregulated the expressions of interleukin-8 (IL-8) and monocyte chemoattractant protein-1 in MKN-45 cells infected with H. pylori. recoflavone 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 21623862-7 2011 Treatment with DA-6034 dissociated the Hsp90 and IKK-gamma complex in H. pylori-infected cells, leading to the inhibition of IL-8 expression. recoflavone 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 21756928-8 2011 Both spontaneous and T/I-induced release of IL-8 and IP-10 was suppressed, although 50muM resveratrol and polydatin up-regulated IL-8. Resveratrol 90-101 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 21756928-8 2011 Both spontaneous and T/I-induced release of IL-8 and IP-10 was suppressed, although 50muM resveratrol and polydatin up-regulated IL-8. polydatin 106-115 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 21756928-9 2011 At this concentration, resveratrol activated both gene expression and de novo synthesis of IL-8 and AhR-mediated mechanisms were involved. Resveratrol 23-34 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 21723850-8 2011 Treating CFBE41o(-) cells with the antioxidant glutathione rescued the IFRD1 protein level closer to control level and also reduced the pro-inflammatory cytokine IL-8 release. Glutathione 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 21700386-1 2011 The presence of NaF in the aqueous suspension of TiO(2) can accelerate the photocatalytic degradation of organic pollutants. titanium dioxide 49-55 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 21715345-10 2011 A significant increase in expression levels of IL-6, TNF-alpha, IL-8, MCP-1, ICAM-1, and BFGF was observed after poly (I:C) RNA stimulation (P < 0.05). Poly I-C 113-123 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 21641110-1 2011 This study explored the possibility of recovering waste powder from photonic industry into two useful resources, sodium fluoride (NaF) and the silica precursor solution. Sodium Fluoride 113-128 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 21669297-7 2011 Three clusters of food, food animal and human NAP1 isolates were highly related by MLVA. mlva 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 21692122-1 2011 Poly(anilineboronic acid) (PABA) nanofibers with U-shaped and ring-shaped morphologies have been synthesized successfully by chemical polymerization of 3-aminophenylboronic acid (APBA) in the presence of cetyltrimethylammonium bromide (CTAB) and NaF. poly(anilineboronic acid) 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 246-249 21692122-1 2011 Poly(anilineboronic acid) (PABA) nanofibers with U-shaped and ring-shaped morphologies have been synthesized successfully by chemical polymerization of 3-aminophenylboronic acid (APBA) in the presence of cetyltrimethylammonium bromide (CTAB) and NaF. 4-Aminobenzoic Acid 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 246-249 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. Cesium 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. Cesium 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. dibenzo-18-crown-6 79-97 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. dibenzo-18-crown-6 79-97 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. dibenzo-18-crown-6 99-105 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. dibenzo-18-crown-6 99-105 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. nafion-117 116-126 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. Cesium 128-130 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. Cesium 128-130 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. Chromium 135-137 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. Chromium 135-137 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. Cesium 128-130 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21707096-1 2011 Temperature dependence study of the self-diffusion coefficient of Cs(+) ion in dibenzo-18-crown-6 (DB18C6) modified Nafion-117 (Cs-Naf-CR) was carried out in the temperature range of 50-65 C. Temperature dependence of water diffusion in Cs-Naf-CR was also studied to understand the mechanism of cation and water transport in the membrane. Cesium 128-130 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 21707096-2 2011 Because of the very slow kinetics of isotopic exchange, self-diffusion measurement of Na(+) in Na-Naf-CR was carried out only at 60 C. The result indicates that self-diffusion behavior is governed by the nature of the cation in which the crown ether was loaded in the membrane matrix. Ether 245-250 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Cesium 39-41 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Cesium 39-41 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Water 53-58 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Water 53-58 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 21636531-5 2011 Interleukin-8 (IL-8) secreted by Het1A cells upon stimulation by capsaicin or acid with/without 4-hydroxy-2-nonenal (HNE) was measured by ELISA. Capsaicin 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 21636531-5 2011 Interleukin-8 (IL-8) secreted by Het1A cells upon stimulation by capsaicin or acid with/without 4-hydroxy-2-nonenal (HNE) was measured by ELISA. Capsaicin 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 21636531-5 2011 Interleukin-8 (IL-8) secreted by Het1A cells upon stimulation by capsaicin or acid with/without 4-hydroxy-2-nonenal (HNE) was measured by ELISA. 4-hydroxy-2-nonenal 96-115 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 21636531-5 2011 Interleukin-8 (IL-8) secreted by Het1A cells upon stimulation by capsaicin or acid with/without 4-hydroxy-2-nonenal (HNE) was measured by ELISA. 4-hydroxy-2-nonenal 96-115 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 21636531-8 2011 Capsaicin and acid induced IL-8 production in Het1A cells, and this production was diminished by antagonists of TRPV1. Capsaicin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 21636531-10 2011 Moreover, IL-8 production in capsaicin-stimulated Het1A cells was enhanced by synthetic HNE treatment. Capsaicin 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 21640702-4 2011 Activation of AhR in vitro by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induced IL-8 expression in MDA-MB 436 and MCF-7 cells in an AhR and RelB dependent manner. Polychlorinated Dibenzodioxins 30-65 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21640702-4 2011 Activation of AhR in vitro by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) induced IL-8 expression in MDA-MB 436 and MCF-7 cells in an AhR and RelB dependent manner. Polychlorinated Dibenzodioxins 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Cesium 62-64 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Cesium 62-64 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Chromium 69-71 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Chromium 69-71 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Cesium 62-64 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Cesium 62-64 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). perfluorosulfonic acid 136-142 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Cesium 62-64 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 21707096-3 2011 The activation energy of diffusion for Cs(+) ion and water in Cs-Naf-CR was found to be much higher than that in the pure Cs(+) form of Nafion (Cs-Naf). Cesium 62-64 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 21707096-4 2011 Water uptake of the membrane was also found to have reduced compared to Cs/Na-Naf. Cesium 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 21531456-8 2011 HT1080 cells treated with Ad/CD-PEG(500)-RGD showed strong induction of apoptosis and suppression of IL-8 and VEGF expression as well. cd-peg 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 21554996-3 2011 Therefore, the current study was aimed to prospectively utilize the baseline IL-8 levels in the HCV infected serum and predicts its role in sustained virological response (SVR) to IFN-alpha+ribavirin therapy, in chronic HCV patients in Pakistan. Ribavirin 190-199 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 20607595-5 2011 The ex vivo release of IL-1beta and IL-6 was not altered by simvastatin, whereas the release of TNF-alpha and IL-8 increased after 6 weeks of simvastatin treatment. Simvastatin 142-153 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 21554996-10 2011 Results of this study suggest that increased levels of IL-8 in HCV infection might be involved in pathogenesis, persistence and resistance to IFN-alpha+ribavirin combination therapy. Ribavirin 152-161 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 21762159-5 2011 o-Cymen-5-ol and zinc chloride have been incorporated into a sodium fluoride (NaF)/silica toothpaste at 0.1%w/w and 0.6%w/w respectively to provide additional benefits. o-cymen-5-ol 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 21567070-11 2011 We demonstrated that prophylactic use of sivelestat mitigated bronchial inflammation by suppressing NE activity and IL-8 levels in the ELF and shortened the duration of SIRS after transthoracic esophagectomy. sivelestat 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 21762159-5 2011 o-Cymen-5-ol and zinc chloride have been incorporated into a sodium fluoride (NaF)/silica toothpaste at 0.1%w/w and 0.6%w/w respectively to provide additional benefits. Sodium Fluoride 61-76 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 21643893-5 2011 After the inflammatory human bronchial epithelial cell line BEAS-2B was treated with dehydroepiandrosterone, levels of proinflammatory cytokines and chemokines were inhibited, including IL-6, IL-8, CCL11, and CCL24. Dehydroepiandrosterone 85-107 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 21471820-12 2011 CONCLUSIONS: Our data suggest divergent effects of tenofovir and AZT on proinflammatory responses in monocytes (CCL3 and IL-8) and PBMCs (CCL3). Tenofovir 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 21471820-12 2011 CONCLUSIONS: Our data suggest divergent effects of tenofovir and AZT on proinflammatory responses in monocytes (CCL3 and IL-8) and PBMCs (CCL3). Zidovudine 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 21570715-9 2011 IL-8 production by macrophages in response to hyaluronan fragment stimulation was compared. Hyaluronic Acid 46-56 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21570715-13 2011 Macrophages from subjects with asthma showed an increase in responsiveness to low-molecular-weight hyaluronan stimulation, as demonstrated by increased IL-8 production. Hyaluronic Acid 99-109 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 21752043-0 2011 Porphyromonas gingivalis lipopolysaccharide lipid A heterogeneity differentially modulates the expression of IL-6 and IL-8 in human gingival fibroblasts. Lipid A 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 21695777-9 2011 The well-dispersed nano-CaF2 may be expected to be a more effective anticaries agent than NaF by providing longer lasting elevations of fluoride concentrations in oral fluids. Fluorides 136-144 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 21555999-0 2011 Hydrogen sulfide inhibits IL-8 expression in human keratinocytes via MAP kinase signaling. Hydrogen Sulfide 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 22103212-3 2011 The nanotube oxide layers were formed on Ti-35Ta-xHf alloy by anodic oxidation method in 1 M H3PO4 electrolytes containing 0.5 wt.% NaF and 0.8 wt.% NaF at room temperature. Oxides 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 149-152 22103212-5 2011 The nano-porous surface of Ti-35Ta-xHf alloys showed in 0.5 wt% NaF solution and nanotubular surface showed in 0.8 wt% NaF solution, respectively. ti-35ta-xhf 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 22103212-6 2011 The highly ordered nanotube layer without regular knots was formed on the Ti-35Ta-15Hf alloy in the 0.5 wt% NaF solution compared to on Ti-35Ta-3Hf and Ti-35Ta-7Hf alloys in 0.8 wt% NaF solution. ti-35ta-15hf 74-86 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 22103213-4 2011 Ti oxide nanotubes were formed on the Ti-35Ta-xZr alloys by anodizing in H3PO4 containing 0.8 wt% NaF solution at 25 degrees C. Anodization was carried out using a scanning potentiostat. titanium dioxide 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 21555999-5 2011 Here, we demonstrate both in vitro and in vivo on primary psoriatic lesions that pharmacological inhibitors of ERKs as well as hydrogen sulfide not only reduce the basal expression and secretion of IL-8, but also interfere with IL-17- and IL-22-induced IL-8 production. Hydrogen Sulfide 127-143 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 21555999-5 2011 Here, we demonstrate both in vitro and in vivo on primary psoriatic lesions that pharmacological inhibitors of ERKs as well as hydrogen sulfide not only reduce the basal expression and secretion of IL-8, but also interfere with IL-17- and IL-22-induced IL-8 production. Hydrogen Sulfide 127-143 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 21651918-13 2011 Moreover, reduction in the levels of IL-6, IL-1Ra, MCP-1/CCL2 and IL-8/CXCL8 was observed in the presence of APE1 Glu allele in BM patients. Glutamic Acid 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 21471820-7 2011 RESULTS: Tenofovir decreased and AZT increased both IL-8 and CCL3 production from monocytes after stimulation with TLR ligands, tumor necrosis factor-alpha, or live pathogens. Zidovudine 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 21651918-13 2011 Moreover, reduction in the levels of IL-6, IL-1Ra, MCP-1/CCL2 and IL-8/CXCL8 was observed in the presence of APE1 Glu allele in BM patients. Glutamic Acid 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 21473897-3 2011 In this in vitro study, we found that nickel, as nickel chloride, could significantly enhance the invasive potential of human lung cancer cells, accompanied by elevated expression of IL-8, TGF-beta, MMP2 and MMP9 in human lung cancer cells. nickel chloride 49-64 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 21830898-10 2011 The novel intervention strategies being developed for EPA and RA, such as IL-6 and IL-8 signaling blockade, may also be considered for chronic CHIKV arthritis. Eicosapentaenoic Acid 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 21518732-11 2011 Furthermore, GSH-EE attenuated Deltapsi(m) depolarization and restored normal IL-8 secretion by CFTR-defective cells. Glutathione 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 21621609-9 2011 In addition, supplementation with reduced GSH inhibited ozone-induced ROS production, NF-kappaB activation, and IL-8 production. Glutathione 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 21621609-10 2011 Taken together, GSTM1 deficiency enhances ozone-induced IL-8 production, which is mediated by generated ROS and subsequent NF-kappaB activation in human bronchial epithelial cells. Reactive Oxygen Species 104-107 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 21670316-8 2011 Likewise, both human blood neutrophils and neutrophil-like HL60 cells produced IL-8 in response to exogenous nucleotides, ATP being the most potent inducer. Adenosine Triphosphate 122-125 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 21643604-4 2011 Finally, almost pure cBN (~90%) crystals are obtained by reacting NH(4)BF(4) and NaN(3) at 250 C and 450 MPa for 24 h, with NaF as the structural induction material. cbn 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 21847358-4 2011 The coculture of PDAC and CAF cell lines enhanced the levels of inflammatory factors including IL-1alpha, IL-6, CXCL8, VEGF-A, CCL20, and COX-2. pdac 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 112-117 21675704-4 2011 Exposure of BEAS-2B and HBE to BaP caused epithelial cells to produce inflammatory cytokines IL-8, which subsequently induced BSMC proliferation and migration. Benzo(a)pyrene 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 21473897-3 2011 In this in vitro study, we found that nickel, as nickel chloride, could significantly enhance the invasive potential of human lung cancer cells, accompanied by elevated expression of IL-8, TGF-beta, MMP2 and MMP9 in human lung cancer cells. Nickel 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 21615439-7 2011 In ex vivo/in vitro studies, bile acids stimulated squamous oesophageal cells and Barrett"s epithelial cells to produce inflammatory mediators (e.g., IL-8 and COX-2) and caused oxidative stress, DNA damage and apoptosis. Bile Acids and Salts 29-39 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 21489599-9 2011 The DeltapH(NaF) was likely a better indicator of the soil"s sulfate adsorption capacity than pH(NaF) as the former excludes the effect of soil acidity. Sulfates 61-68 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 20870895-13 2011 The NF-kappaB inhibitors gliotoxin and parthenolide increased apoptosis and decreased IL-8 and CXCR2 expression. Gliotoxin 25-34 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 20870895-13 2011 The NF-kappaB inhibitors gliotoxin and parthenolide increased apoptosis and decreased IL-8 and CXCR2 expression. parthenolide 39-51 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 20870895-14 2011 Also, the p38MAPK inhibitor SB202190 increased apoptosis and decreased IL-8 expression but had no effect on CXCR2 expression. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 21143697-4 2011 We show that upregulation of the two NF-kB target genes show differences in pH preference, with IL-8 being preferentially upregulated by DCA at neutral pH, and IkB being upregulated by neutral DCA, acidic DCA, and acid alone. Dichloroacetic Acid 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 21143697-4 2011 We show that upregulation of the two NF-kB target genes show differences in pH preference, with IL-8 being preferentially upregulated by DCA at neutral pH, and IkB being upregulated by neutral DCA, acidic DCA, and acid alone. Dichloroacetic Acid 193-196 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 21143697-4 2011 We show that upregulation of the two NF-kB target genes show differences in pH preference, with IL-8 being preferentially upregulated by DCA at neutral pH, and IkB being upregulated by neutral DCA, acidic DCA, and acid alone. Dichloroacetic Acid 193-196 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 21307878-6 2011 In the human T-cell line, MOLT-14, GM-CSF and IL-8 transcripts were increased and stabilized in cells treated with crude APP or purified procyanidins. app 121-124 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 22435021-8 2011 On the contrary both LPS and CoCl(2) increased significantly IL-8. cobaltous chloride 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 21765609-0 2011 Relationship between dietary folate intake and plasma monocyte chemoattractant protein-1 and interleukin-8 in heart failure patients. Folic Acid 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 93-106 21765609-8 2011 Dietary folate intake was found as a primary influencing factor on plasma levels of monocyte chemoattractant protein-1 (p<0.005, R(2) = 0.20) and interleukin-8 (p<0.001, R(2) = 0.32) through a stepwise multiple linear regression analysis. Folic Acid 8-14 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 21765609-9 2011 Dietary folate intake was significantly associated with plasma levels of monocyte chemoattractant protein-1 and interleukin-8 which indicates dietary folate may have a potentially beneficial role in the prevention and treatment of heart failure. Folic Acid 8-14 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 21765609-9 2011 Dietary folate intake was significantly associated with plasma levels of monocyte chemoattractant protein-1 and interleukin-8 which indicates dietary folate may have a potentially beneficial role in the prevention and treatment of heart failure. Folic Acid 150-156 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 21307878-6 2011 In the human T-cell line, MOLT-14, GM-CSF and IL-8 transcripts were increased and stabilized in cells treated with crude APP or purified procyanidins. Proanthocyanidins 137-149 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 21623439-2 2011 Here, we report a one-pot synthesis of doxorubicin-doped silica nanoparticles (Dox/SiNPs) by using sodium fluoride (NaF) catalyzed hydrolysis of tetraethyl orthosilicate in a water-in-oil microemulsion. Doxorubicin 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21623439-2 2011 Here, we report a one-pot synthesis of doxorubicin-doped silica nanoparticles (Dox/SiNPs) by using sodium fluoride (NaF) catalyzed hydrolysis of tetraethyl orthosilicate in a water-in-oil microemulsion. Silicon Dioxide 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21623439-2 2011 Here, we report a one-pot synthesis of doxorubicin-doped silica nanoparticles (Dox/SiNPs) by using sodium fluoride (NaF) catalyzed hydrolysis of tetraethyl orthosilicate in a water-in-oil microemulsion. Doxorubicin 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21623439-2 2011 Here, we report a one-pot synthesis of doxorubicin-doped silica nanoparticles (Dox/SiNPs) by using sodium fluoride (NaF) catalyzed hydrolysis of tetraethyl orthosilicate in a water-in-oil microemulsion. sinps 83-88 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21623439-2 2011 Here, we report a one-pot synthesis of doxorubicin-doped silica nanoparticles (Dox/SiNPs) by using sodium fluoride (NaF) catalyzed hydrolysis of tetraethyl orthosilicate in a water-in-oil microemulsion. Sodium Fluoride 99-114 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21623439-2 2011 Here, we report a one-pot synthesis of doxorubicin-doped silica nanoparticles (Dox/SiNPs) by using sodium fluoride (NaF) catalyzed hydrolysis of tetraethyl orthosilicate in a water-in-oil microemulsion. tetraethoxysilane 145-169 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21623439-2 2011 Here, we report a one-pot synthesis of doxorubicin-doped silica nanoparticles (Dox/SiNPs) by using sodium fluoride (NaF) catalyzed hydrolysis of tetraethyl orthosilicate in a water-in-oil microemulsion. Water 175-180 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21623439-2 2011 Here, we report a one-pot synthesis of doxorubicin-doped silica nanoparticles (Dox/SiNPs) by using sodium fluoride (NaF) catalyzed hydrolysis of tetraethyl orthosilicate in a water-in-oil microemulsion. Oils 184-187 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 21338276-5 2011 The most important findings were: (i) TTA reduced plasma total cholesterol, non HDL-cholesterol, LDL/HDL cholesterol ratio, triglycerides and total fatty acids; (ii) TTA decreased plasma TNF-alpha, IL-8 and VCAM-1; and (iii) plasma fatty acid composition changed with an increased level of monounsaturated fatty acids and decreased n-3 polyunsaturated fatty acids. 1-(carboxymethylthio)tetradecane 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 21338276-5 2011 The most important findings were: (i) TTA reduced plasma total cholesterol, non HDL-cholesterol, LDL/HDL cholesterol ratio, triglycerides and total fatty acids; (ii) TTA decreased plasma TNF-alpha, IL-8 and VCAM-1; and (iii) plasma fatty acid composition changed with an increased level of monounsaturated fatty acids and decreased n-3 polyunsaturated fatty acids. 1-(carboxymethylthio)tetradecane 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 21899065-6 2011 In Group 1, wiferon produced an immunomodulatory effect, by lowering IL-8 concentrations to the level observed in Group 3. wiferon 12-19 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 21486191-9 2011 The hydrolysis was catalyzed by plasma esterase because NaF (sodium fluoride: a general esterase inhibitor) inhibited WS070117 hydrolysis and metabolite production. Sodium Fluoride 61-76 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 21385008-5 2011 Moreover, PL induced a strong cell actin cytoskeletal re-organization that persisted up to 24 h. The accelerated wound closure promoted by PL, in either presence or absence of serum, was associated with a high expression of the inflammatory cytokine interleukin-8. pl 10-12 C-X-C motif chemokine ligand 8 Homo sapiens 250-263 21385008-5 2011 Moreover, PL induced a strong cell actin cytoskeletal re-organization that persisted up to 24 h. The accelerated wound closure promoted by PL, in either presence or absence of serum, was associated with a high expression of the inflammatory cytokine interleukin-8. pl 139-141 C-X-C motif chemokine ligand 8 Homo sapiens 250-263 21385008-6 2011 Further, after 24 h PL treatment, confluent keratinocytes also expressed low amounts of interleukin-8 and of the antimicrobial peptide neutrophil gelatinase-associated lipocalin, which dramatically increased under inflammatory conditions. pl 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 21486191-9 2011 The hydrolysis was catalyzed by plasma esterase because NaF (sodium fluoride: a general esterase inhibitor) inhibited WS070117 hydrolysis and metabolite production. O2',O3',O5'-triacetyl-N6-(3-hydroxylaniline)adenosine 118-126 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 21666550-5 2011 Two major lignans, schizandrin (Sch) and gomisin A (Gom A), were identified and shown to induce interleukin (IL)-8, macrophage inflammatory protein-1beta (MIP-1beta), and granulocyte-macrophage-colony stimulating factor (GM-CSF) release by THP-1 cells. Lignans 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 96-114 21621513-6 2011 Furthermore, pretreatment with casuarinin decreased TNF-alpha-induced pro-inflammatory mediators, such as IL-1beta, IL-6, IL-8, and MCP-1. casuarinin 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 21666550-5 2011 Two major lignans, schizandrin (Sch) and gomisin A (Gom A), were identified and shown to induce interleukin (IL)-8, macrophage inflammatory protein-1beta (MIP-1beta), and granulocyte-macrophage-colony stimulating factor (GM-CSF) release by THP-1 cells. schizandrin 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 96-114 21666550-5 2011 Two major lignans, schizandrin (Sch) and gomisin A (Gom A), were identified and shown to induce interleukin (IL)-8, macrophage inflammatory protein-1beta (MIP-1beta), and granulocyte-macrophage-colony stimulating factor (GM-CSF) release by THP-1 cells. schizandrin 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 96-114 21474440-3 2011 In the absence of glucocorticoids, both decreasing GR protein levels by an siRNA strategy and results with the GR antagonist RU486 suggest a role for the unliganded GR in reduction of TNFalpha-induced IL-6 and IL-8 mRNA levels in End1/E6E7 cells. Mifepristone 125-130 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 21666550-5 2011 Two major lignans, schizandrin (Sch) and gomisin A (Gom A), were identified and shown to induce interleukin (IL)-8, macrophage inflammatory protein-1beta (MIP-1beta), and granulocyte-macrophage-colony stimulating factor (GM-CSF) release by THP-1 cells. schizandrol B 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 96-114 21666550-5 2011 Two major lignans, schizandrin (Sch) and gomisin A (Gom A), were identified and shown to induce interleukin (IL)-8, macrophage inflammatory protein-1beta (MIP-1beta), and granulocyte-macrophage-colony stimulating factor (GM-CSF) release by THP-1 cells. schizandrol B 52-57 C-X-C motif chemokine ligand 8 Homo sapiens 96-114 21330456-0 2011 Nebulized hypertonic saline decreases IL-8 in sputum of patients with cystic fibrosis. hypertonic 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 21330456-0 2011 Nebulized hypertonic saline decreases IL-8 in sputum of patients with cystic fibrosis. Sodium Chloride 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 21330456-2 2011 IL-8 is protected from proteolytic degradation in the airways by binding to glycosaminoglycans, while remaining active. Glycosaminoglycans 76-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21330456-3 2011 Evidence that increased hypertonicity of airway secretions induced by hypertonic saline treatment alters levels of IL-8 is lacking. Sodium Chloride 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 21330456-4 2011 OBJECTIVES: To investigate the antiinflammatory effect of hypertonic saline (HTS) treatment within the CF lung by focusing on IL-8. Sodium Chloride 58-75 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 21330456-9 2011 High sodium concentrations also liberate IL-8 in CF BALF in vitro, and in vivo in CF sputum from patients receiving aerosolized HTS, resulting in degradation of IL-8 and decreased neutrophil chemotactic efficiency. Sodium 5-11 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 21330456-9 2011 High sodium concentrations also liberate IL-8 in CF BALF in vitro, and in vivo in CF sputum from patients receiving aerosolized HTS, resulting in degradation of IL-8 and decreased neutrophil chemotactic efficiency. Sodium 5-11 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 21330456-10 2011 CONCLUSIONS: Glycosaminoglycans possess the ability to influence the chemokine profile of the CF lung by binding and stabilizing IL-8, which promotes neutrophil chemotaxis and activation. Glycosaminoglycans 13-31 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 21330456-11 2011 Nebulized hypertonic saline treatment disrupts the interaction between glycosaminoglycans and IL-8, rendering IL-8 susceptible to proteolytic degradation with subsequent decrease in neutrophil chemotaxis, thereby facilitating resolution of inflammation. Sodium Chloride 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 21330456-11 2011 Nebulized hypertonic saline treatment disrupts the interaction between glycosaminoglycans and IL-8, rendering IL-8 susceptible to proteolytic degradation with subsequent decrease in neutrophil chemotaxis, thereby facilitating resolution of inflammation. Sodium Chloride 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 21337319-8 2011 Stimulation with poly(I-C) induced the activation of IFN regulatory factor 3 (IRF-3), NF-kappaB, and activator protein 1 (AP-1) c-Jun as well as the subsequent production of IFNbeta, CXCL8, and MMP-3. Poly I-C 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 183-188 21421269-5 2011 Beta-TCP 1 mum did not induce any cytokine after 6 h but slightly increases TNF-alpha, IL-1beta and IL-8 release after 18 h. Larger particles (32 and 40 mum) consistently caused higher levels of cytokine release by increasing the fraction of cytokine producing monocytes. beta-tricalcium phosphate 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 21272678-12 2011 In human mononuclear leukocyte, isoforskolin (50, 100, and 200 muM) and dexamethasone (10 muM) pre-incubation lowered lipopolysaccharide (2 mug/mL) induced secretion of the cytokine TNF-alpha, and interleukins (IL)-1beta, IL-6, and IL-8. Dexamethasone 72-85 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 21420233-6 2011 This results in combinatorial inhibition of NFkappaB activity by gallic acid, which results in potent inhibition of NFkappaB target genes involved in inflammation, metastasis, anti-apoptosis and angiogenesis, such as IL-6, IL-8, COX2, CXCR4, XIAP, bcl2, VEGF. Gallic Acid 65-76 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 21631990-13 2011 The reduction of VCAM-1, resulting from increased IL-8, could be blocked by the MEK inhibitor, PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 95-102 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 21143185-4 2011 There is recent evidence that the NF-kappaB-dependent gene expression of interleukin 8, interleukin 6, cyclooxygenase-2, tumor necrosis factor and interleukin 33 in directly irradiated cells produced the cytokines and prostaglandin E2 with autocrine/paracrine functions, which further activated signaling pathways and induced NF-kappaB-dependent gene expression in bystander cells. Dinoprostone 218-234 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 21376115-5 2011 Removal of intracellular ROS by N-acetylcysteine reduced the AMPK activation and IL-8 induction. Reactive Oxygen Species 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21376115-5 2011 Removal of intracellular ROS by N-acetylcysteine reduced the AMPK activation and IL-8 induction. Acetylcysteine 32-48 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21376115-7 2011 Abrogation of the activation of NF-kappaB and STAT3 by BAY11-7085 and AG490, respectively, attenuated the IL-8 induction. BAY 11-7085 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 21376115-7 2011 Abrogation of the activation of NF-kappaB and STAT3 by BAY11-7085 and AG490, respectively, attenuated the IL-8 induction. alpha-cyano-(3,4-dihydroxy)-N-benzylcinnamide 70-75 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 21376115-9 2011 Thus, a novel NADPH oxidase-dependent, ROS-sensitive AMPK signaling is important for CS-induced IL-8 production in LECs and possibly lung inflammation. Reactive Oxygen Species 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 21376115-9 2011 Thus, a novel NADPH oxidase-dependent, ROS-sensitive AMPK signaling is important for CS-induced IL-8 production in LECs and possibly lung inflammation. Cesium 85-87 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 20626232-8 2011 In addition, MW attenuated the PMACI-stimulated expression of pro-inflammatory cytokines such as tumor necrosis factor-alpha, interleukin-1beta (IL-1beta), IL-6, and IL-8 in human mast cells. pmaci 31-36 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 21272678-13 2011 In conclusion, pretreatment with isoforskolin attenuates lipopolysaccharide-induced acute lung injury in several models, and it is involved in down-regulation of inflammatory responses and proinflammatory cytokines TNF-alpha, IL-1beta, IL-6, and IL-8. Isoforskolin 33-45 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 21524887-8 2011 When NHK was stimulated by TGF-beta1, paraformaldehyde-fixed, and co-cultured with THP-1 cells, IL-8 production by THP-1 cells was increased compared to THP-1 cells only. paraform 38-54 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 21427353-4 2011 When exposed to PAM at 10 microM, NHOK, not NHOF, underwent senescence: NHOK overexpressed senescence-associated beta-galactosidase (SA-beta-Gal), p16INK4A, IL-6, and IL-8. Pamidronate 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 21413027-3 2011 Here, we investigated the role of phosphatidylcholine-specific phospholipase C (PC-PLC) in LPS-induced IL-8 and MCP-1 production in VECs. Phosphatidylcholines 34-53 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 21413027-5 2011 Blocking the function of PC-PLC by exploiting the neutralization antibody of PC-PLC or tricyclodecan-9-yl-xanthogenate (D609), an inhibitor of PC-PLC, significantly inhibited LPS-induced production of IL-8 and MCP-1 in HUVECs. tricyclodecan-9-yl-xanthogenate 87-118 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 21413027-5 2011 Blocking the function of PC-PLC by exploiting the neutralization antibody of PC-PLC or tricyclodecan-9-yl-xanthogenate (D609), an inhibitor of PC-PLC, significantly inhibited LPS-induced production of IL-8 and MCP-1 in HUVECs. tricyclodecane-9-yl-xanthogenate 120-124 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 21384150-6 2011 dTBP2 inhibited the induction of IL-8 by dTCTP from BEAS-2B cells. dtbp2 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 21401388-3 2011 CS activates epithelial cells to secrete chemokines such as interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) that recruit neutrophils and macrophages to the lung. Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 21401388-3 2011 CS activates epithelial cells to secrete chemokines such as interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) that recruit neutrophils and macrophages to the lung. Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 21401388-9 2011 Production of both chemokines was significantly reduced with SFN given prior to CSE; SFN inhibited IL-8 and MCP-1 gene expression at the transcription level. sulforaphane 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 21770169-4 2011 In addition, we used a serum-containing medium to prevent the possible effects of IL-8 protein adsorption in the nano-ZnO and nano-TiO2. Zinc Oxide 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 21384150-6 2011 dTBP2 inhibited the induction of IL-8 by dTCTP from BEAS-2B cells. dtctp 41-46 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 21338358-8 2011 IL-8 up-regulation by LL-37 was completely abrogated by 20 mum U0126, consistent with transient phosphorylation of p44/42 MAP kinases. U 0126 63-68 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21770169-4 2011 In addition, we used a serum-containing medium to prevent the possible effects of IL-8 protein adsorption in the nano-ZnO and nano-TiO2. titanium dioxide 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 21770169-7 2011 On the other hand, the IL-8 protein had a marked influence on the adsorption of nano-TiO2 in the serum-free medium. titanium dioxide 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 21770169-8 2011 While only at 100 microg mL(-1) of nano-ZnO, an influence on the adsorption of IL-8 was observed. Zinc Oxide 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 21338358-9 2011 Moreover, pretreatment with Brilliant Blue G (a selective antagonist of the P2X(7) receptor) and the neutralizing antibody against P2X(7) blocked IL-8 up-regulation in a dose-dependent manner, consistent with expression of the P2X(7) receptor in HGFs. coomassie Brilliant Blue 28-44 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 21609799-7 2011 SP cotreatment restores DMVEC proliferation (211%) and tube formation (152%), and decreases IL-8 expression (34%) in DMVECs exposed to hyperglycemic conditions. dmvecs 117-123 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 20174873-0 2011 Effects of 15-deoxy- 12,14-prostaglandin J2 on the production of IL-8 and the expression of Toll-like receptor 2 in human primary keratinocytes stimulated with lipopolysaccharide. 15-deoxy-delta(12,14)-prostaglandin J2 11-43 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 20174873-6 2011 15d-PGJ(2) decreased TLR2 mRNA, increased IL-8 production, and suppressed NF-kappaB activity. 15d-pgj 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 20174873-10 2011 Thus, 15d-PGJ(2) can have both anti- and pro-inflammatory effects, and 15d-PGJ(2)-mediated IL-8 up-regulation is related to the mitogen-activated protein kinase (MAPK) and NF-kappaB signaling pathways. 15d-pgj 71-78 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 21745629-0 2011 Capsaicin attenuates palmitate-induced expression of macrophage inflammatory protein 1 and interleukin 8 by increasing palmitate oxidation and reducing c-Jun activation in THP-1 (human acute monocytic leukemia cell) cells. Capsaicin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 21533553-4 2011 Exposure of HaCaT cells to CoCl(2) reduced cell viability and caused overproduction of reactive oxygen species (ROS) and oversecretion of interleukin-6 (IL-6) and interleukin-8 (IL-8). cobaltous chloride 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 163-176 21533553-4 2011 Exposure of HaCaT cells to CoCl(2) reduced cell viability and caused overproduction of reactive oxygen species (ROS) and oversecretion of interleukin-6 (IL-6) and interleukin-8 (IL-8). cobaltous chloride 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 21533553-6 2011 Inhibition of COX-2 by NS-398, a selective inhibitor of COX-2, significantly repressed the cytotoxicity, as well as secretion of IL-6 and IL-8 induced by CoCl(2). N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 23-29 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 21533553-6 2011 Inhibition of COX-2 by NS-398, a selective inhibitor of COX-2, significantly repressed the cytotoxicity, as well as secretion of IL-6 and IL-8 induced by CoCl(2). cocl 154-158 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 21745629-9 2011 Our data suggest that the attenuation of palmitate-induced MIP-1 and IL-8 gene expressions by capsaicin is associated with reduced activation of c-Jun N-terminal kinase, c-Jun, and p38 and preserved beta-oxidation activity. Palmitates 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 21745629-9 2011 Our data suggest that the attenuation of palmitate-induced MIP-1 and IL-8 gene expressions by capsaicin is associated with reduced activation of c-Jun N-terminal kinase, c-Jun, and p38 and preserved beta-oxidation activity. Capsaicin 94-103 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 21533553-8 2011 Neutralizing anti-IL-6 or anti-IL-8 antibody statistically alleviated CoCl(2)-induced cytotoxicity in HaCaT cells. cobaltous chloride 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 21745629-0 2011 Capsaicin attenuates palmitate-induced expression of macrophage inflammatory protein 1 and interleukin 8 by increasing palmitate oxidation and reducing c-Jun activation in THP-1 (human acute monocytic leukemia cell) cells. Palmitates 119-128 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 21745629-2 2011 In this study, we tested the hypothesis that the anti-inflammatory activity of capsaicin can be used to improve free fatty acid (FFA)-induced inflammation by reducing gene expression of macrophage inflammatory protein 1 (MIP-1) and interleukin 8 (IL-8) in THP-1 (human acute monocytic leukemia cell) macrophages. Capsaicin 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 232-245 21745629-2 2011 In this study, we tested the hypothesis that the anti-inflammatory activity of capsaicin can be used to improve free fatty acid (FFA)-induced inflammation by reducing gene expression of macrophage inflammatory protein 1 (MIP-1) and interleukin 8 (IL-8) in THP-1 (human acute monocytic leukemia cell) macrophages. Capsaicin 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 21745629-2 2011 In this study, we tested the hypothesis that the anti-inflammatory activity of capsaicin can be used to improve free fatty acid (FFA)-induced inflammation by reducing gene expression of macrophage inflammatory protein 1 (MIP-1) and interleukin 8 (IL-8) in THP-1 (human acute monocytic leukemia cell) macrophages. Fatty Acids, Nonesterified 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 232-245 21745629-2 2011 In this study, we tested the hypothesis that the anti-inflammatory activity of capsaicin can be used to improve free fatty acid (FFA)-induced inflammation by reducing gene expression of macrophage inflammatory protein 1 (MIP-1) and interleukin 8 (IL-8) in THP-1 (human acute monocytic leukemia cell) macrophages. Fatty Acids, Nonesterified 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 21745629-3 2011 To investigate whether capsaicin ameliorates palmitate-induced MIP-1 and IL-8 gene expressions, we treated THP-1 cells with palmitate in the presence or absence of capsaicin and measured MIP-1 and IL-8 by real-time polymerase chain reaction. Capsaicin 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 21745629-3 2011 To investigate whether capsaicin ameliorates palmitate-induced MIP-1 and IL-8 gene expressions, we treated THP-1 cells with palmitate in the presence or absence of capsaicin and measured MIP-1 and IL-8 by real-time polymerase chain reaction. Palmitates 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 21745629-0 2011 Capsaicin attenuates palmitate-induced expression of macrophage inflammatory protein 1 and interleukin 8 by increasing palmitate oxidation and reducing c-Jun activation in THP-1 (human acute monocytic leukemia cell) cells. Palmitates 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 21745629-4 2011 To elucidate the mechanism by which capsaicin effects on palmitate-induced MIP-1 and IL-8 gene expressions, we performed immunoblotting with stress kinase-related antibodies and measured palmitate oxidation and palmitate oxidation-related gene expression. Capsaicin 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 21745629-4 2011 To elucidate the mechanism by which capsaicin effects on palmitate-induced MIP-1 and IL-8 gene expressions, we performed immunoblotting with stress kinase-related antibodies and measured palmitate oxidation and palmitate oxidation-related gene expression. Palmitates 57-66 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 21745629-5 2011 Palmitate and stearate but not the unsaturated FFA oleate significantly increased MIP-1 and IL-8 expressions in THP-1 macrophages. Palmitates 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 20817708-0 2011 Signalling pathway of isophorone diisocyanate-responsive interleukin-8 in airway smooth muscle cells. isophorone diisocyanate 22-45 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 21745629-5 2011 Palmitate and stearate but not the unsaturated FFA oleate significantly increased MIP-1 and IL-8 expressions in THP-1 macrophages. Stearates 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21745629-6 2011 Treatment with capsaicin or FFA oxidation stimulators inhibited palmitate-induced MIP-1 and IL-8 expressions in THP-1 macrophages. Capsaicin 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21745629-6 2011 Treatment with capsaicin or FFA oxidation stimulators inhibited palmitate-induced MIP-1 and IL-8 expressions in THP-1 macrophages. Palmitates 64-73 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21454676-3 2011 We previously demonstrated that the anti-inflammatory drugs dexamethasone and ibuprofen suppress NF-kappaB; however, only dexamethasone down-regulates cytokine-induced IL-8, highlighting the importance of non-NF-kappaB mechanisms. Dexamethasone 122-135 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 21454676-6 2011 We observed that dexamethasone, but not ibuprofen, destabilizes IL-8 mRNA and up-regulates MKP-1 mRNA. Dexamethasone 17-30 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 21454676-7 2011 Further, siRNA silencing of MKP-1, via p38 MAPK, leads to IL-8 overproduction and diminishes the anti-IL-8 potential of dexamethasone. Dexamethasone 120-133 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21454676-9 2011 By contrast, direct inhibition of p38 MAPK (inhibitor SB203580) efficiently suppresses IL-8 with potency comparable with dexamethasone. SB 203580 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 21454676-10 2011 Similar to dexamethasone, SB203580 decreases IL-8 mRNA stability. SB 203580 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 21703102-1 2011 The aim of this study was to assess the impact of a single nasal allergen challenge (NAC) on levels of eotaxin and IL-8 and the inflammatory cells in upper and lower airways of allergic rhinitis (AR) patients. nac 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 21703102-7 2011 Post-NAC IL-8 levels were significantly increased in NLF (p < 00001) but not in sputum (p = 0.080) of AR subjects. nac 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 21299717-6 2011 Indeed, chromatin immunoprecipitation (ChIP) analysis showed that events related to transcriptional activation of the IL-8 gene region in response to TNF-alpha, including recruitment of RNA polymerase II (Pol II), were compromised in the presence of TSA. trichostatin A 250-253 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 20817708-8 2011 Our study suggests that inhibition of IL-8 or IL-8-mediated FAK/ERK/Rnd3 signalling is an attractive therapeutic target for IPDI-mediated asthma. isophorone diisocyanate 124-128 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 20817708-8 2011 Our study suggests that inhibition of IL-8 or IL-8-mediated FAK/ERK/Rnd3 signalling is an attractive therapeutic target for IPDI-mediated asthma. isophorone diisocyanate 124-128 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 21536200-9 2011 Corrosion products, probably sodium aluminum fluoride (Na(3)AlF(6)), were observed on the implants after immersion in both NaF solutions for both time periods. cryolite 29-53 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 21536200-9 2011 Corrosion products, probably sodium aluminum fluoride (Na(3)AlF(6)), were observed on the implants after immersion in both NaF solutions for both time periods. cryolite 55-67 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 21615989-2 2011 Water-soluble extract of S. aureus cell lysate strongly induced human interleukin- 8 in human mast cell line-1 and mouse interleukin-6 in mouse bone marrow-derived mast cells. Water 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 70-84 20817708-7 2011 FAK and ERK1/2 inhibitor also decreased IPDI-BEAS-2B-CM-, IPDI-HBEC-CM- and recombinant human IL-8-mediated BSMC proliferation and migration, whereas blocking Rnd3 using small interfering RNA failed to affect BSMC proliferation, suggesting that Rnd3 was only involved in the regulation of BSMC migration. bsmc 108-112 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 20501519-6 2011 Using an antibody array approach, we found that ATO increased the production of several cytokines, with interleukin 8 (IL-8) being the predominant one. Arsenic Trioxide 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 20501519-10 2011 Also, we conclude that the production of IL-8 is not induced by a caspase-4-dependent mechanism, suggesting that ATO-induced caspase-4 activation is involved in other as yet unidentified functions in human neutrophils. Arsenic Trioxide 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 21761011-1 2011 The aim of this study was to examine the degree and prevalence of regional (aorta) and global (cardiac) fluorine-18-sodium fluoride ((18)F-NaF) uptake by positron emission tomography (PET)-computed tomography (CT) as evidence for calcification in the atherosclerotic plaques in the aorta and the heart as a function of age. fluorine-18-sodium fluoride 104-131 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 20501519-6 2011 Using an antibody array approach, we found that ATO increased the production of several cytokines, with interleukin 8 (IL-8) being the predominant one. Arsenic Trioxide 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 20501519-7 2011 We confirmed that ATO increased the production of IL-8 by enzyme-linked-immunosorbent assay (ELISA). Arsenic Trioxide 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 21605007-5 2011 Following ozone exposure, these purines remained correlated with IL-6, IL-8, and TNF-alpha (r = 0.37-0.68). Purines 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 20648559-8 2011 Growth inhibition studies showed that IL-8 overexpression lead to a significant resistance to oxaliplatin (p < 0.0001). Oxaliplatin 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 20648559-9 2011 Inhibition of IL-8 overexpression with small interfering RNA reversed the observed increases in tumorigenic functions and oxaliplatin resistance, suggesting that IL-8 not only provides a proliferative advantage but also promotes the metastatic potential of colon cancer cells. Oxaliplatin 122-133 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 20648559-9 2011 Inhibition of IL-8 overexpression with small interfering RNA reversed the observed increases in tumorigenic functions and oxaliplatin resistance, suggesting that IL-8 not only provides a proliferative advantage but also promotes the metastatic potential of colon cancer cells. Oxaliplatin 122-133 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 21605007-4 2011 RESULTS: At baseline, the purines AMP and hypoxanthine correlated with multiple inflammatory markers including neutrophil counts and the cytokines interleukin (IL)-6, IL-8, tumor necrosis factor alpha (TNF-alpha), and IL-1beta (r ranged from 0.41 to 0.66, all P < 0.05). Purines 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 21531299-0 2011 Development and validation of an anion-exchange HPLC method for the determination of fluoride content and radiochemical purity in [18F]NaF. Fluorides 85-93 C-X-C motif chemokine ligand 8 Homo sapiens 135-138 21605007-4 2011 RESULTS: At baseline, the purines AMP and hypoxanthine correlated with multiple inflammatory markers including neutrophil counts and the cytokines interleukin (IL)-6, IL-8, tumor necrosis factor alpha (TNF-alpha), and IL-1beta (r ranged from 0.41 to 0.66, all P < 0.05). Adenosine Monophosphate 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 21399866-8 2011 The long-term TMZ-treated astroglioma cells, but not the Hs683 oligodendroglioma cells, developed in vivo a certain level of resistance to TMZ, which correlated with the up- regulation of CXCL2, CXCL3 and CXCL8 expression in the U373 and T98G astroglioma cells. Temozolomide 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 205-210 21300705-6 2011 Corticosteroid sensitivity was evaluated by the inhibition of tumor necrosis factor alpha (TNFalpha)-induced interleukin 8 (IL-8) production by budesonide. Budesonide 144-154 C-X-C motif chemokine ligand 8 Homo sapiens 109-122 21300705-6 2011 Corticosteroid sensitivity was evaluated by the inhibition of tumor necrosis factor alpha (TNFalpha)-induced interleukin 8 (IL-8) production by budesonide. Budesonide 144-154 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 21531299-1 2011 (18)F-labeled sodium fluoride ([(18)F]NaF) is a useful bone imaging agent that has been demonstrated to be significantly more accurate than (99m)Tc-labeled methylene diphosphonate for the detection of both sclerotic and lytic lesions in various malignancies. Sodium Fluoride 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 21531299-3 2011 The method described for fluoride analysis uses an isocratic elution of NaF in a Hamilton anion-exchange column using a mobile phase that consists of 7.5 mM sodium carbonate and 0.018 mM potassium thiocyanate. Fluorides 25-33 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 21531299-14 2011 Therefore, the method can be successfully performed for routine analysis of fluoride content in [(18)F]NaF radiopharmaceuticals and reduce the time required for analysis. Fluorides 76-84 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 21488183-3 2011 Therefore, the aim of this study was to investigate the signal transduction pathway of nLDL-dependent IL-8 production and the effect of IL-8 on hAoSMCs migration. haosmcs 144-151 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 21193553-7 2011 Addition of the p38 inhibitor SB203580 to Dianeal resulted in dampened IL-8 release (-55%; p < 0.05) and basal HSP70 expression, and unchanged LDH release. SB 203580 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 21193553-9 2011 CONCLUSION: These data confirm concordant p38-dependent upregulation of IL-8 and HSP70 following exposure to bioincompatible PDF. pdf 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 21172926-8 2011 Treatment with SB202190 (p38-MAPK inhibitor) or PD98059 (ERK inhibitor) inhibited AGE-BSA-induced IL-6 and IL-8 expression. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 21172926-8 2011 Treatment with SB202190 (p38-MAPK inhibitor) or PD98059 (ERK inhibitor) inhibited AGE-BSA-induced IL-6 and IL-8 expression. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 21172926-9 2011 However, SP600125 (JNK inhibitor) had no effect on AGE-BSA-induced IL-6 expression but inhibited the expression of IL-8. pyrazolanthrone 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 21826964-5 2011 However, BS and 18F-NaF PET/CT are more sensitive for sclerotic lesions, as a decreased 18F-FDG uptake in this subtype of lesion has been reported. Fluorodeoxyglucose F18 88-95 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 21297082-3 2011 Exposure of BEAS-2B and HBE to ANE, sANE, and arecoline increased interleukin 8 (IL-8) and Regulated upon Activation, Normal T-cell Expressed, and Secreted (RANTES) production. ane 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 21297082-3 2011 Exposure of BEAS-2B and HBE to ANE, sANE, and arecoline increased interleukin 8 (IL-8) and Regulated upon Activation, Normal T-cell Expressed, and Secreted (RANTES) production. ane 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21297082-3 2011 Exposure of BEAS-2B and HBE to ANE, sANE, and arecoline increased interleukin 8 (IL-8) and Regulated upon Activation, Normal T-cell Expressed, and Secreted (RANTES) production. sane 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 21297082-3 2011 Exposure of BEAS-2B and HBE to ANE, sANE, and arecoline increased interleukin 8 (IL-8) and Regulated upon Activation, Normal T-cell Expressed, and Secreted (RANTES) production. sane 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21297082-3 2011 Exposure of BEAS-2B and HBE to ANE, sANE, and arecoline increased interleukin 8 (IL-8) and Regulated upon Activation, Normal T-cell Expressed, and Secreted (RANTES) production. Arecoline 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 21297082-3 2011 Exposure of BEAS-2B and HBE to ANE, sANE, and arecoline increased interleukin 8 (IL-8) and Regulated upon Activation, Normal T-cell Expressed, and Secreted (RANTES) production. Arecoline 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21488183-7 2011 IL-8-induced migration of hAoSMCs was evaluated by counting the cell numbers moved to lower chamber using Transwell plates. haosmcs 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21488183-8 2011 RESULTS: nLDL-induced IL-8 production was completely blocked by preincubation of hAoSMCs with pertussis toxin (PTX), which inhibited nLDL-dependent p38 MAPK phosphorylation. haosmcs 81-88 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 21488183-10 2011 Pretreatment of PEG-Cat prevented nLDL-induced p38 MAPK phosphorylation and IL-8 production, which was partly mimicked by treatment with exogenous H2O22. Polyethylene Glycols 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 21800536-6 2011 The results suggest that sodium nitrite could induce SMMC-7721 EMT by increased secretion of TGF-beta1 and IL-8. Sodium Nitrite 25-39 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 21488183-10 2011 Pretreatment of PEG-Cat prevented nLDL-induced p38 MAPK phosphorylation and IL-8 production, which was partly mimicked by treatment with exogenous H2O22. h2o22 147-152 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 21800536-6 2011 The results suggest that sodium nitrite could induce SMMC-7721 EMT by increased secretion of TGF-beta1 and IL-8. smmc 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 21488183-12 2011 CONCLUSION: PTX-sensitive G-protein coupled receptor-dependent H2O2 generation by nLDL plays a critical role in IL-8 production in hAoSMC, and IL-8 may contribute to atherogenesis through increased migration of hAoSMCs. Hydrogen Peroxide 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 21284934-8 2011 Hence, to survey the functionality of indomethacin after stimulation with contact allergens IL-8 and TRIM16 regulation was measured by a DC-based in vitro assay. Indomethacin 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21424022-4 2011 The produced DADB can be readily separated from the sodium fluoride (NaF) by-product by a purification procedure using liquid ammonia at -78 C. The thermal decomposition behavior of DADB was studied using synchronous thermal analyses, particularly in comparison with AB. dadb 183-187 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 21329685-5 2011 Moreover the two highest concentrations of both fluoride-containing bioglasses and NaF caused increase of nitrite (a stable derivative of NO) levels in the culture supernatant, which was inhibited by l-NMMA, erythrocytes, PTIO and SOD/catalase, and increase of intracellular NO synthase (NOS) activity. Nitrites 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 21329685-5 2011 Moreover the two highest concentrations of both fluoride-containing bioglasses and NaF caused increase of nitrite (a stable derivative of NO) levels in the culture supernatant, which was inhibited by l-NMMA, erythrocytes, PTIO and SOD/catalase, and increase of intracellular NO synthase (NOS) activity. omega-N-Methylarginine 200-206 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 21329685-6 2011 The incubation with bioglasses or NaF increased also the phosphorylation of Ser(1177) in the endothelial NOS isoform. Serine 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 21413719-0 2011 High temperature NMR study of aluminum metal influence on speciation in molten NaF-AlF3 fluorides. Aluminum 30-44 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 21284934-9 2011 Incubation with isoeugenol after pre-treatment with indomethacin leads to increased IL-8 and TRIM16 gene expression. isoeugenol 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21496221-4 2011 In this article we have investigated the possible use of bergamot extracts (Citrus bergamia Risso) and their identified components to alter the expression of IL-8 associated with the cystic fibrosis airway pathology. bergamot oil 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 21284934-9 2011 Incubation with isoeugenol after pre-treatment with indomethacin leads to increased IL-8 and TRIM16 gene expression. Indomethacin 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21496221-10 2011 CONCLUSIONS: These obtained results clearly indicate that bergapten and citropten are strong inhibitors of IL-8 expression and could be proposed for further studies to verify possible anti-inflammatory properties to reduce lung inflammation in CF patients. 5-Methoxypsoralen 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 21395877-6 2011 RESULTS: Budesonide and dexamethasone produced a concentration-dependent inhibition of the LPS-induced IL-8 and TNF-alpha secretion with an E(max) about 90% of inhibition, which was reduced by approximately 30% in the presence of H(2)O(2) or CSE. Budesonide 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 21496221-10 2011 CONCLUSIONS: These obtained results clearly indicate that bergapten and citropten are strong inhibitors of IL-8 expression and could be proposed for further studies to verify possible anti-inflammatory properties to reduce lung inflammation in CF patients. 5,7-dimethoxycoumarin 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 21241417-8 2011 Importantly, catechins, in particular ECG, inhibited TNFalpha-induced activation of NF-kappaB and consequently secretion of pro-inflammatory and invasion promoting proteins like IL-8 and uPA. Catechin 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 21241417-8 2011 Importantly, catechins, in particular ECG, inhibited TNFalpha-induced activation of NF-kappaB and consequently secretion of pro-inflammatory and invasion promoting proteins like IL-8 and uPA. epicatechin gallate 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 21370925-4 2011 Exposure of BEAS-2B and HBE to DBP caused epithelial cells to produce inflammatory cytokines IL-8 and RANTES, which subsequently induced BSMC proliferation and migration. bsmc 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 21370925-5 2011 Depleting both IL-8 and RANTES completely reversed the effect of DBP-BEAS-2B-CM and DBP-HBE-CM-mediated BSMC proliferation and migration, suggesting this effect is a synergistic influence of IL-8 and RANTES. bsmc 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 21370925-5 2011 Depleting both IL-8 and RANTES completely reversed the effect of DBP-BEAS-2B-CM and DBP-HBE-CM-mediated BSMC proliferation and migration, suggesting this effect is a synergistic influence of IL-8 and RANTES. bsmc 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 21468084-0 2011 Chitosan oligosaccharides suppress LPS-induced IL-8 expression in human umbilical vein endothelial cells through blockade of p38 and Akt protein kinases. chitosan oligosaccharides 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 21468084-1 2011 AIM: To investigate whether and how COS inhibited IL-8 production in LPS-induced human umbilical vein endothelial cells (HUVECs). carbonyl sulfide 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 21468084-4 2011 RESULTS: COS 50-200 mug/mL exerted a significant inhibitory effect on LPS 100 ng/mL-induced IL-8 expression in HUVECs at both the transcriptional and translational levels. carbonyl sulfide 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21468084-7 2011 Further, the over-expression of LPS-induced IL-8 mRNA in HUVECs was suppressed by a p38 MAPK inhibitor (SB203580, 25 mumol/L) or a phosphatidylinositol 3-kinase (PI3K) inhibitor (LY294002, 50 mumol/L). SB 203580 104-112 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 21468084-7 2011 Further, the over-expression of LPS-induced IL-8 mRNA in HUVECs was suppressed by a p38 MAPK inhibitor (SB203580, 25 mumol/L) or a phosphatidylinositol 3-kinase (PI3K) inhibitor (LY294002, 50 mumol/L). 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 179-187 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 21468084-8 2011 CONCLUSION: COS inhibited LPS-induced IL-8 expression in HUVECs through the blockade of the p38 MAPK and PI3K/Akt signaling pathways. carbonyl sulfide 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 21442636-0 2011 Circulating levels of MCP-1, sIL-2R, IL-15, and IL-8 predict anemia response to pomalidomide therapy in myelofibrosis. pomalidomide 80-92 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 21395877-6 2011 RESULTS: Budesonide and dexamethasone produced a concentration-dependent inhibition of the LPS-induced IL-8 and TNF-alpha secretion with an E(max) about 90% of inhibition, which was reduced by approximately 30% in the presence of H(2)O(2) or CSE. Dexamethasone 24-37 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 21395877-6 2011 RESULTS: Budesonide and dexamethasone produced a concentration-dependent inhibition of the LPS-induced IL-8 and TNF-alpha secretion with an E(max) about 90% of inhibition, which was reduced by approximately 30% in the presence of H(2)O(2) or CSE. Water 230-235 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 21316925-0 2011 An environmental contaminant, benzo(a)pyrene, induces oxidative stress-mediated interleukin-8 production in human keratinocytes via the aryl hydrocarbon receptor signaling pathway. Benzo(a)pyrene 30-44 C-X-C motif chemokine ligand 8 Homo sapiens 80-93 21300765-0 2011 Lactate influx through the endothelial cell monocarboxylate transporter MCT1 supports an NF-kappaB/IL-8 pathway that drives tumor angiogenesis. Lactic Acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 21300765-4 2011 We found that lactate could enter endothelial cells through the monocarboxylate transporter MCT-1, trigger the phosphorylation/degradation of IkappaBalpha, and then stimulate an autocrine NF-kappaB/IL-8 (CXCL8) pathway driving cell migration and tube formation. Lactic Acid 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 21300765-4 2011 We found that lactate could enter endothelial cells through the monocarboxylate transporter MCT-1, trigger the phosphorylation/degradation of IkappaBalpha, and then stimulate an autocrine NF-kappaB/IL-8 (CXCL8) pathway driving cell migration and tube formation. Lactic Acid 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 204-209 21300765-7 2011 Finally, we documented in mouse xenograft models of human colorectal and breast cancer that lactate release from tumor cells through the MCT4 (and not MCT1) transporter is sufficient to stimulate IL-8-dependent angiogenesis and tumor growth. Lactic Acid 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 21300765-8 2011 In conclusion, our findings establish a signaling role for lactate in endothelial cells and they identify the lactate/NF-kappaB/IL-8 pathway as an important link between tumor metabolism and angiogenesis. Lactic Acid 110-117 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 21173096-5 2011 Neutrophils treated with simvastatin were submitted to interleukin 8-stimulated chemotaxis assays. Simvastatin 25-36 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 21173096-10 2011 Furthermore, intercellular adhesion molecule-1 expression was significantly abrogated on tumor necrosis factor-alpha-stimulated endothelium incubated with simvastatin, and statin treatment inhibited the interleukin-8-stimulated migration of both control and sickle cell disease neutrophils. Simvastatin 155-166 C-X-C motif chemokine ligand 8 Homo sapiens 203-216 21267611-11 2011 Co-incubation of BEAS-2B cells with both gadolinium and iron resulted in diminished release of IL-8 relative to levels of the cytokine following incubation with gadolinium alone. Gadolinium 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 21267611-11 2011 Co-incubation of BEAS-2B cells with both gadolinium and iron resulted in diminished release of IL-8 relative to levels of the cytokine following incubation with gadolinium alone. Iron 56-60 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 21267611-11 2011 Co-incubation of BEAS-2B cells with both gadolinium and iron resulted in diminished release of IL-8 relative to levels of the cytokine following incubation with gadolinium alone. Gadolinium 161-171 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 21316925-11 2011 Furthermore, the addition of N-acetyl cystein or catalase cancelled the IL-8 production by BaP, indicating that ROS production is essential for IL-8 production. Reactive Oxygen Species 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 21368236-5 2011 The objective of the current study is to test the hypothesis that chemokines (eotaxin, RANTES, IL-8, and MIP-1alpha) can directly influence ASMC mass by increasing the rate of proliferation or enhancing the survival of these cells. asmc 140-144 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 21368236-10 2011 In a concentration-dependent manner, chemokines including eotaxin, RANTES, IL-8, and MIP-1alpha increased ASMC"s [(3)H]thymidine incorporation and DNA synthesis. asmc 106-110 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 21316925-11 2011 Furthermore, the addition of N-acetyl cystein or catalase cancelled the IL-8 production by BaP, indicating that ROS production is essential for IL-8 production. Reactive Oxygen Species 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 21368236-10 2011 In a concentration-dependent manner, chemokines including eotaxin, RANTES, IL-8, and MIP-1alpha increased ASMC"s [(3)H]thymidine incorporation and DNA synthesis. Thymidine 119-128 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 21368236-11 2011 IL-8, eotaxin, and MIP-1alpha decreased the rate of apoptosis of ASMCs compared with the matched controls. asmcs 65-70 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21316925-12 2011 RESULTS: This data highlights AhR-ROS-dependent regulation of IL-8 in NHEKs by BaP, providing a plausible explanation, at least in part, for why cigarette smoking exacerbates IL-8-related skin diseases such as psoriasis, palmoplantar pustulosis and acne. Reactive Oxygen Species 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 21316925-12 2011 RESULTS: This data highlights AhR-ROS-dependent regulation of IL-8 in NHEKs by BaP, providing a plausible explanation, at least in part, for why cigarette smoking exacerbates IL-8-related skin diseases such as psoriasis, palmoplantar pustulosis and acne. Reactive Oxygen Species 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 21193045-3 2011 Firstly, the immunomodulatory activity of the antibiotic was tested in vitro using Caco-2 intestinal epithelial cells and RAW 264.7 macrophages; minocycline was able to inhibit IL-8 and nitrite production, respectively. Minocycline 145-156 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 21322034-2 2011 They present a conserved 3D structure, so-called IL8-like chemokine fold, which is supported by conserved cysteines forming intra-molecular disulfide bonds. Cysteine 106-115 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 21042230-9 2011 Statistical analysis revealed that only IL-8 (rs4073, -251A>T) showed significant differences in genotype and allele frequency between the control and APN or ALN cases. apholate 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 21042230-9 2011 Statistical analysis revealed that only IL-8 (rs4073, -251A>T) showed significant differences in genotype and allele frequency between the control and APN or ALN cases. aln 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 21042230-10 2011 Following the elimination of vesicoureteral reflux, which is a significant risk factor for severe parenchymal infection, a single SNP in IL-8 (rs4073) was found to be associated with clinically severe ALN. aln 201-204 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 21322034-2 2011 They present a conserved 3D structure, so-called IL8-like chemokine fold, which is supported by conserved cysteines forming intra-molecular disulfide bonds. Disulfides 140-149 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 21316309-0 2011 Metformin modulates IL-8, IL-1beta, ICAM and IGFBP-1 expression in human endometrial stromal cells. Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 21322034-4 2011 However, it has been shown that different patterns can provide disulfide bonds fitting into an IL8-like architecture, which has been the key to identify new remote homologues of the IL8-like chemokine family. Disulfides 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 21316309-7 2011 The negative effect of insulin on IL-8 (4.8 fold) and IL-1beta (9.3 fold) gene expression was similarly found in cells incubated with metformin. Metformin 134-143 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 21322034-4 2011 However, it has been shown that different patterns can provide disulfide bonds fitting into an IL8-like architecture, which has been the key to identify new remote homologues of the IL8-like chemokine family. Disulfides 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 21266580-3 2011 Thrombin-induced IL-8/CXCL8 release and IL-8/CXCL8-luciferase activity were attenuated by a PI3K inhibitor (LY294002), an Akt inhibitor (1-L-6-hydroxymethyl-chiro-inositol-2-((R)-2-O-methyl-3-O-octadecylcarbonate)), and the dominant negative mutants of Rac1 (RacN17) and Akt (AktDN). 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 21232592-8 2011 IL-8 secretion into the basolateral culture medium was increased at ZnO-NP concentrations of 5 mug/ml (P<0.05), as shown by ELISA. zno-np 68-74 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21566865-6 2011 RESULTS: The mean values of fluoride concentration in the control group, NaF group and Duraphat varnish group were(0.0406+-0.0234)wt%,(0.1006+-0.1040)wt% and (0.1844+-0.1293)wt%,respectively.The concentration of fluoride in the Duraphat varnish group was significantly higher than that in the NaF group (P<0.01). Fluorides 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 21266580-3 2011 Thrombin-induced IL-8/CXCL8 release and IL-8/CXCL8-luciferase activity were attenuated by a PI3K inhibitor (LY294002), an Akt inhibitor (1-L-6-hydroxymethyl-chiro-inositol-2-((R)-2-O-methyl-3-O-octadecylcarbonate)), and the dominant negative mutants of Rac1 (RacN17) and Akt (AktDN). 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 22-27 21266580-3 2011 Thrombin-induced IL-8/CXCL8 release and IL-8/CXCL8-luciferase activity were attenuated by a PI3K inhibitor (LY294002), an Akt inhibitor (1-L-6-hydroxymethyl-chiro-inositol-2-((R)-2-O-methyl-3-O-octadecylcarbonate)), and the dominant negative mutants of Rac1 (RacN17) and Akt (AktDN). 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 21266580-3 2011 Thrombin-induced IL-8/CXCL8 release and IL-8/CXCL8-luciferase activity were attenuated by a PI3K inhibitor (LY294002), an Akt inhibitor (1-L-6-hydroxymethyl-chiro-inositol-2-((R)-2-O-methyl-3-O-octadecylcarbonate)), and the dominant negative mutants of Rac1 (RacN17) and Akt (AktDN). 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 45-50 21266580-3 2011 Thrombin-induced IL-8/CXCL8 release and IL-8/CXCL8-luciferase activity were attenuated by a PI3K inhibitor (LY294002), an Akt inhibitor (1-L-6-hydroxymethyl-chiro-inositol-2-((R)-2-O-methyl-3-O-octadecylcarbonate)), and the dominant negative mutants of Rac1 (RacN17) and Akt (AktDN). 1L-6-hydroxymethyl-chiro-inositol 2(R)-2-O-methyl-3-O-octadecylcarbonate 137-212 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 21266580-3 2011 Thrombin-induced IL-8/CXCL8 release and IL-8/CXCL8-luciferase activity were attenuated by a PI3K inhibitor (LY294002), an Akt inhibitor (1-L-6-hydroxymethyl-chiro-inositol-2-((R)-2-O-methyl-3-O-octadecylcarbonate)), and the dominant negative mutants of Rac1 (RacN17) and Akt (AktDN). 1L-6-hydroxymethyl-chiro-inositol 2(R)-2-O-methyl-3-O-octadecylcarbonate 137-212 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 21266580-3 2011 Thrombin-induced IL-8/CXCL8 release and IL-8/CXCL8-luciferase activity were attenuated by a PI3K inhibitor (LY294002), an Akt inhibitor (1-L-6-hydroxymethyl-chiro-inositol-2-((R)-2-O-methyl-3-O-octadecylcarbonate)), and the dominant negative mutants of Rac1 (RacN17) and Akt (AktDN). 1L-6-hydroxymethyl-chiro-inositol 2(R)-2-O-methyl-3-O-octadecylcarbonate 137-212 C-X-C motif chemokine ligand 8 Homo sapiens 45-50 21423807-10 2011 IL-8 production by carcinoma cells can be modulated by low doses of cyclophosphamide at the transcription level. Cyclophosphamide 68-84 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21399573-7 2011 This concentration of AC-PACs also significantly increased the secretion of IL-8 (6-fold) and inhibited the secretion of both MMP-2 and MMP-9. ac-pacs 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 20463293-7 2011 The stimulation of IL-8 cytokine release was completely attenuated by treatment with the JNK-specific inhibitor, SP600125. pyrazolanthrone 113-121 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 21193404-8 2011 Interestingly, alpha(1)-antitrypsin, in addition to its ability to neutralize NE and protease-3, can also bind heme and neutralize heme-induced IL-8 from CFBE41o(-) cells. Heme 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 21248183-6 2011 RESULTS: Vitamin A-supplemented children with fecal MCP-1 or IL-8 concentrations less than the median of detectable concentrations and IL-10 concentrations of at least median concentrations had longer durations of EPEC infection than did children in the placebo group. Vitamin A 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 21388551-10 2011 Oxysterols can induce the production of inflammatory cytokines such as interleukin-8 and interleukin-1beta. Oxysterols 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 21193404-5 2011 One of the effects of this is the release of heme, and in this study we show that heme stimulates IL-8 and IL-10 protein production from DeltaF508 CFBE41o(-) bronchial epithelial cells. Heme 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 21193404-6 2011 In addition, heme-induced IL-8 expression utilizes a novel pathway involving meprin, EGF receptor, and MyD88. Heme 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20870757-17 2011 Simvastatin decreased bronchoalveolar lavage IL-8 by 2.5-fold (P = 0.04). Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 21356375-0 2011 Novel roles for hypoxia and prostaglandin E2 in the regulation of IL-8 during endometrial repair. Dinoprostone 28-44 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 21189358-6 2011 Dex suppressed genes in immune/inflammatory (IL-6, IL-8, and MCP-1, expressed in nonadipocytes) and proapoptotic pathways, yet induced genes related to the acute-phase response (SAA, factor D, haptoglobin, and RBP4, expressed in adipocytes) and stress/defense response. Dexamethasone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 21679503-12 2011 UFH or LMWH inhibited tumor necrosis factor alpha (10 ng/mL)-induced secretion of MUC5AC and IL-8 from NCI-H292 cells in a dose-dependent manner (0.01-10 IU/mL). Heparin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 21356375-7 2011 IL-8 was increased by PGE(2) and hypoxia in secretory but not proliferative explants, which suggests that exposure to progesterone is essential. Prostaglandins E 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21679503-12 2011 UFH or LMWH inhibited tumor necrosis factor alpha (10 ng/mL)-induced secretion of MUC5AC and IL-8 from NCI-H292 cells in a dose-dependent manner (0.01-10 IU/mL). Heparin, Low-Molecular-Weight 7-11 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 21679503-14 2011 CONCLUSION: These results indicate that heparin inhibits airway mucus hypersecretion in airway epithelial cells directly and indirectly through the suppression of IL-8 secretion and neutrophil infiltration. Heparin 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 21356375-7 2011 IL-8 was increased by PGE(2) and hypoxia in secretory but not proliferative explants, which suggests that exposure to progesterone is essential. Progesterone 118-130 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21356375-9 2011 Epithelial cells treated simultaneously with PGE(2) and hypoxia demonstrated synergistic increases in IL-8. Prostaglandins E 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 21356375-10 2011 Inhibition of HIF-1 by short hairpin RNA abolished hypoxic IL-8 induction, and inhibition of NF-kappaB by an adenoviral dominant negative inhibitor decreased PGE(2)-induced IL-8 expression (P > 0.05). Prostaglandins E 158-161 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 21356375-12 2011 Progesterone withdrawal, hypoxia, and PGE(2) regulate endometrial IL-8 by acting via HIF-1 and NF-kappaB. Dinoprostone 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 21215400-10 2011 The AcLDL-induced IL-8 production was inhibited by LY294002 and filipin. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. Mebendazole 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. Albendazole 156-167 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. Albendazole 169-172 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. Fenbendazole 175-187 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. Fenbendazole 189-192 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. oxibendazole 198-210 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. oxibendazole 212-215 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. albendazole sulfoxide 229-250 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. Praziquantel 254-266 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-4 2011 The release of interleukin (IL)-8 and tumor necrosis factor (TNF) alpha from human monocytic THP-1 cells was significantly increased by treatment with MBZ, albendazole (ABZ), fenbendazole (FBZ), or oxibendazole (OBZ), but not by albendazole sulfoxide or praziquantel, suggesting that MBZ and structurally similar drugs can stimulate monocytes and increase the release of pro-inflammatory cytokines. Mebendazole 284-287 C-X-C motif chemokine ligand 8 Homo sapiens 15-33 20848085-6 2011 Pretreatment with the MAP kinase/ERK kinase 1/2 inhibitor U0126 significantly suppressed the increase of IL-8 and TNFalpha levels by MBZ, ABZ, FBZ, or OBZ treatment in THP-1 cells, but the p38 mitogen-activated protein kinase inhibitor SB203580 or JNK1/2 inhibitor SP600125 did not. U 0126 58-63 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 20848085-6 2011 Pretreatment with the MAP kinase/ERK kinase 1/2 inhibitor U0126 significantly suppressed the increase of IL-8 and TNFalpha levels by MBZ, ABZ, FBZ, or OBZ treatment in THP-1 cells, but the p38 mitogen-activated protein kinase inhibitor SB203580 or JNK1/2 inhibitor SP600125 did not. Albendazole 138-141 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 20848085-7 2011 These results suggested that an ERK1/2 pathway plays an important role in the release of IL-8 and TNFalpha in THP-1 cells treated with MBZ and structurally similar drugs. Mebendazole 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 21216561-5 2011 The results showed that atorvastatin significantly decreased the expression of six cytokines (IL-6, IL-8, IL-1, PAI-1, TGF-beta1, TGF-beta2) and five chemokines (CCL2, CCL7, CCL13, CCL18, CXCL1). Atorvastatin 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 21121988-9 2011 Decrease in lesion progression was observed in Groups A, B and C. CONCLUSIONS: The 500 ppm NaF dentifrice demonstrated remineralization of carious lesions by virtue of a significant decrease in lesion depth; whereas dentifrices that contained AmF, MFP and MFP with xylitol decelerated the progression of demineralization. Xylitol 265-272 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 21073547-5 2011 In vitro studies in human lung epithelial cell lines showed that levofloxacin led to a dose-related reduction in IL-6 and IL-8 concentrations, with 300 mug mL(-1) resulting in the reduction of levels of IL-6 by fourfold and IL-8 by twofold (P<0.05); in contrast, tobramycin increased IL-6 levels by 50%, but had no effect on IL-8. Levofloxacin 65-77 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 21073547-5 2011 In vitro studies in human lung epithelial cell lines showed that levofloxacin led to a dose-related reduction in IL-6 and IL-8 concentrations, with 300 mug mL(-1) resulting in the reduction of levels of IL-6 by fourfold and IL-8 by twofold (P<0.05); in contrast, tobramycin increased IL-6 levels by 50%, but had no effect on IL-8. Levofloxacin 65-77 C-X-C motif chemokine ligand 8 Homo sapiens 224-228 21073547-5 2011 In vitro studies in human lung epithelial cell lines showed that levofloxacin led to a dose-related reduction in IL-6 and IL-8 concentrations, with 300 mug mL(-1) resulting in the reduction of levels of IL-6 by fourfold and IL-8 by twofold (P<0.05); in contrast, tobramycin increased IL-6 levels by 50%, but had no effect on IL-8. Levofloxacin 65-77 C-X-C motif chemokine ligand 8 Homo sapiens 224-228 20832139-10 2011 Interestingly, whereas Fas-mediated inhibition of phagocytosis and oxidative burst could be prevented by the broad range caspase inhibitor t-butoxycarbonyl-aspartyl(O-methyl)-fluoromethyl ketone (BocD-fmk), the chemotactic activity in response to IL-8 was unaffected. ammonium ferrous sulfate 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 20832139-10 2011 Interestingly, whereas Fas-mediated inhibition of phagocytosis and oxidative burst could be prevented by the broad range caspase inhibitor t-butoxycarbonyl-aspartyl(O-methyl)-fluoromethyl ketone (BocD-fmk), the chemotactic activity in response to IL-8 was unaffected. t-butoxycarbonyl-aspartyl(o-methyl)-fluoromethyl ketone 139-194 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 20832139-10 2011 Interestingly, whereas Fas-mediated inhibition of phagocytosis and oxidative burst could be prevented by the broad range caspase inhibitor t-butoxycarbonyl-aspartyl(O-methyl)-fluoromethyl ketone (BocD-fmk), the chemotactic activity in response to IL-8 was unaffected. bocd-fmk 196-204 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 21254387-9 2011 CaCl(2) induced expression of IL-8 and TNFalpha in whole blood cultures. Calcium Chloride 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 21147194-10 2011 The overall cumulative fluoride ion re-release according to the fluoride treatments was APF and NaF solution>dentifrice. Fluorides 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 21176887-4 2011 RESULTS: CFTR F508 AECs secrete more CXCL8 in response to PsaDM than their wild type counterpart, which can be reversed by addition of extracellular glutathione or incubating AECs at 27 C to favour folding and expression of CFTR at the cell membrane. Glutathione 149-160 C-X-C motif chemokine ligand 8 Homo sapiens 37-42 21282043-9 2011 Consequently, quercetin suppressed UV irradiation-induced expression of inflammatory cytokines IL-1beta (~60%), IL-6 (~80%), IL-8 (~76%) and TNF-alpha (~69%). Quercetin 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 20940323-9 2011 Based on the analysis of the cytokine/chemokine content of sDC-SIGN culture supernatants, we identified IFN-gamma and CXCL8/IL-8 as inducers of sDC-SIGN production by MoDC. S-[2-(Aminosulfonyl)ethyl]-D-Cysteine 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 20940323-9 2011 Based on the analysis of the cytokine/chemokine content of sDC-SIGN culture supernatants, we identified IFN-gamma and CXCL8/IL-8 as inducers of sDC-SIGN production by MoDC. S-[2-(Aminosulfonyl)ethyl]-D-Cysteine 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 20940323-9 2011 Based on the analysis of the cytokine/chemokine content of sDC-SIGN culture supernatants, we identified IFN-gamma and CXCL8/IL-8 as inducers of sDC-SIGN production by MoDC. S-[2-(Aminosulfonyl)ethyl]-D-Cysteine 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 20940323-9 2011 Based on the analysis of the cytokine/chemokine content of sDC-SIGN culture supernatants, we identified IFN-gamma and CXCL8/IL-8 as inducers of sDC-SIGN production by MoDC. S-[2-(Aminosulfonyl)ethyl]-D-Cysteine 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 21348878-4 2011 Accordingly, this review examines how varying degrees of CR-induced weight loss (i.e., >10%, 5-10%, and <5% from baseline) impact plasma levels and expression of adiponectin, leptin, resistin, interleukin 6 (IL-6), interleukin 8 (IL-8), monocyte chemotactic protein 1 (MCP-1), and retinol-binding protein 4 (RBP-4). Chromium 57-59 C-X-C motif chemokine ligand 8 Homo sapiens 221-234 21485100-7 2011 ROS stimulates alveolar macrophages and neutrophils to release inflammatory cytokines, such as TNF-alpha, IL-8, IFN-gamma, IL-6 and IL-1beta. Reactive Oxygen Species 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 20713976-8 2011 Exposure of HPMC to 3.4-DGE resulted in suppression of HSP, and increased release of LDH, IL-6 and IL-8. hydroxypropylmethylcellulose-lactose matrix 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 20713976-8 2011 Exposure of HPMC to 3.4-DGE resulted in suppression of HSP, and increased release of LDH, IL-6 and IL-8. 3,4-dideoxyglucosone-3-ene 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 21348878-4 2011 Accordingly, this review examines how varying degrees of CR-induced weight loss (i.e., >10%, 5-10%, and <5% from baseline) impact plasma levels and expression of adiponectin, leptin, resistin, interleukin 6 (IL-6), interleukin 8 (IL-8), monocyte chemotactic protein 1 (MCP-1), and retinol-binding protein 4 (RBP-4). Chromium 57-59 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 21319354-7 2011 After cardiopulmonary bypass, IL-6, IL-8 and MDA levels were significantly increased, and the SOD level was significantly reduced in both two groups, but PF group exhibited lower IL-6, IL-8 and MDA levels and higher SOD levels than the MF group (p < 0.05, respectively). pyrazofurin 154-156 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 21299226-8 2011 Simulations of the CXCL-8 dimer complexed with a 24-mer heparin fragment and of the CXCL-8-receptor peptide complex revealed that Arg60, Lys64, and Arg68 in the dimer bind to cyclitols in a horseshoe pattern, defining a region which is spatially distinct from the receptor binding site. Cyclitols 175-184 C-X-C motif chemokine ligand 8 Homo sapiens 19-25 21299226-9 2011 There appears to be an optimum number of sulfates and an optimum length of alkyl spacers required for the interaction of cyclitol inhibitors with the dimeric form of CXCL-8. Sulfates 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 166-172 21299226-9 2011 There appears to be an optimum number of sulfates and an optimum length of alkyl spacers required for the interaction of cyclitol inhibitors with the dimeric form of CXCL-8. Cyclitols 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 166-172 21352551-6 2011 Peak respiratory burst activity was seen at 15-20 min, and superoxide levels returned to baseline by 1 h. IL-8 release was dependent on both membrane-associated CD14 (mCD14) and Toll-like receptor 4 (TLR4. Superoxides 59-69 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 21352574-8 2011 In mucosa and polyp epithelial cells, mometasone inhibited this induced secretion while desloratadine inhibited IL-6 and IL-8. desloratadine 88-101 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 21212273-6 2011 In addition, inhibition of IGF-1R activation by either its specific antagonist AG1024 or siRNA against IGF-1 significantly reduces NT-induced IL-8 expression and NF-kappaB-dependent reporter gene expression. tyrphostin AG 1024 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 21275387-0 2011 Quercetin reduces neutrophil recruitment induced by CXCL8, LTB4, and fMLP: inhibition of actin polymerization. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 52-57 21352551-8 2011 Moreover, treatment with lovastatin inhibited LPS-dependent IL-8 release and superoxide production. Lovastatin 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 21345194-0 2011 Effects of ulinastatin and docataxel on breast tumor growth and expression of IL-6, IL-8, and TNF-alpha. docataxel 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21091433-6 2011 A fluoride anion was found in the active site when NaF was added to the crystallization buffer. fluoride anion 2-16 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 21345222-8 2011 OPN301 significantly decreased Pam3CSK4-induced cytokine production of tumour necrosis factor alpha (TNF-alpha), IL-1beta, IL-6, interferon (IFN)-gamma and IL-8 compared to IgG control in RA PBMCs and SFMCs cultures (all P < 0.05). opn301 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 21177635-8 2011 ERK1/2 pathway inhibitor, UO126, failed IL-8 promoter activity, whereas p38 MAPK inhibitor, SB203580, decreased the stabilization of IL-8 messenger RNA following V. parahaemolyticus infection. SB 203580 92-100 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 21146504-3 2011 The PPARbeta/delta agonist GW501516 inhibited the increase caused by TNF-alpha in the mRNA levels of the NF-kappaB target genes interleukin 8 (IL-8), TNF-alpha and thymic stromal lymphopoietin (TSLP). GW 501516 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 21146504-3 2011 The PPARbeta/delta agonist GW501516 inhibited the increase caused by TNF-alpha in the mRNA levels of the NF-kappaB target genes interleukin 8 (IL-8), TNF-alpha and thymic stromal lymphopoietin (TSLP). GW 501516 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 21146504-11 2011 Finally, the reduction in IL-8 mRNA levels following GW501516 treatment in TNF-alpha-stimulated cells was abolished in the presence of the PPARbeta/delta antagonist GSK0660, the AMPK inhibitor compound C and the SIRT1 inhibitor sirtinol, indicating that the effects of GW501516 on NF-kappaB activity were dependent on PPARbeta/delta, AMPK and SIRT1, respectively. GW 501516 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 21146504-11 2011 Finally, the reduction in IL-8 mRNA levels following GW501516 treatment in TNF-alpha-stimulated cells was abolished in the presence of the PPARbeta/delta antagonist GSK0660, the AMPK inhibitor compound C and the SIRT1 inhibitor sirtinol, indicating that the effects of GW501516 on NF-kappaB activity were dependent on PPARbeta/delta, AMPK and SIRT1, respectively. GSK0660 165-172 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 21146504-11 2011 Finally, the reduction in IL-8 mRNA levels following GW501516 treatment in TNF-alpha-stimulated cells was abolished in the presence of the PPARbeta/delta antagonist GSK0660, the AMPK inhibitor compound C and the SIRT1 inhibitor sirtinol, indicating that the effects of GW501516 on NF-kappaB activity were dependent on PPARbeta/delta, AMPK and SIRT1, respectively. sirtinol 228-236 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 21146504-11 2011 Finally, the reduction in IL-8 mRNA levels following GW501516 treatment in TNF-alpha-stimulated cells was abolished in the presence of the PPARbeta/delta antagonist GSK0660, the AMPK inhibitor compound C and the SIRT1 inhibitor sirtinol, indicating that the effects of GW501516 on NF-kappaB activity were dependent on PPARbeta/delta, AMPK and SIRT1, respectively. GW 501516 269-277 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20843633-7 2011 Increasing carbon chain length of straight chain alcohols positively correlated with their ability to inhibit detection of tumor necrosis factor alpha (TNF-alpha) and interleukin 10 (IL-10), but not with the detection of interleukin 6 (IL-6), interleukin 8, (IL-8), and interleukin 12 (IL-12). Carbon 11-17 C-X-C motif chemokine ligand 8 Homo sapiens 243-256 21177434-8 2011 Formation of neutrophil extracellular traps was significantly enhanced by 5-LOX inhibition but attenuated by HETE-PE, whereas 5-HETE-PE enhanced superoxide and interleukin-8 generation. 5-hete-pe 126-135 C-X-C motif chemokine ligand 8 Homo sapiens 160-173 21213342-8 2011 The method is applied to a data set from a prospective clinical trial investigating the effectiveness of silver diamine fluoride (SDF) and sodium fluoride (NaF) varnish in arresting active dentin caries in the Chinese preschool children. Sodium Fluoride 139-154 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 21347371-6 2011 SAGEs bound LL-37 and inhibited interleukin-8 production induced by LL-37 in cultured human keratinocytes. sages 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 20843633-7 2011 Increasing carbon chain length of straight chain alcohols positively correlated with their ability to inhibit detection of tumor necrosis factor alpha (TNF-alpha) and interleukin 10 (IL-10), but not with the detection of interleukin 6 (IL-6), interleukin 8, (IL-8), and interleukin 12 (IL-12). Carbon 11-17 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 20843633-7 2011 Increasing carbon chain length of straight chain alcohols positively correlated with their ability to inhibit detection of tumor necrosis factor alpha (TNF-alpha) and interleukin 10 (IL-10), but not with the detection of interleukin 6 (IL-6), interleukin 8, (IL-8), and interleukin 12 (IL-12). Alcohols 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 243-256 20946124-11 2011 Dexamethasone (100 nM) partially inhibited release of both IL-6 and IL-8. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20843633-7 2011 Increasing carbon chain length of straight chain alcohols positively correlated with their ability to inhibit detection of tumor necrosis factor alpha (TNF-alpha) and interleukin 10 (IL-10), but not with the detection of interleukin 6 (IL-6), interleukin 8, (IL-8), and interleukin 12 (IL-12). Alcohols 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 20946124-8 2011 In human chondrocytes, BK increased release (over 24 h) of IL-6 and IL-8, effects blocked by MEN16132 but not by the B1 receptor antagonist Lys-[Leu8][desArg9]BK. (4-amino-5-(4-(4-(2,4-dichloro-3-(2,4-dimethyl-8-quinolyloxymethyl)phenylsulfonamido)tetrahydro-2H-4-pyranoylcarbonyl)piperazino)-5-oxopentyl)(trimethyl)ammonium 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 21156725-6 2011 PPACK, U0126, U-73122, 2-APB or GF-109203X suppressed the increases in production of IL-8, GROalpha and MCP-1 induced by thrombin (P < 0.001, P <0.001 and P <0.001, respectively). 2-aminoethoxydiphenyl borate 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 20940111-8 2011 Cord blood cytokines (IL-1beta, IL-8, IFNgamma, TNFalpha) showed a U-shaped association with U-As at GW30. u-as 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 21156725-6 2011 PPACK, U0126, U-73122, 2-APB or GF-109203X suppressed the increases in production of IL-8, GROalpha and MCP-1 induced by thrombin (P < 0.001, P <0.001 and P <0.001, respectively). U 0126 7-12 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 21156725-6 2011 PPACK, U0126, U-73122, 2-APB or GF-109203X suppressed the increases in production of IL-8, GROalpha and MCP-1 induced by thrombin (P < 0.001, P <0.001 and P <0.001, respectively). 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 20680429-3 2011 In the present study, we report effects of sodium fluoride (NaF) on the differentiation of a human epithelial cell line, HaCaT. Sodium Fluoride 43-58 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 21156725-6 2011 PPACK, U0126, U-73122, 2-APB or GF-109203X suppressed the increases in production of IL-8, GROalpha and MCP-1 induced by thrombin (P < 0.001, P <0.001 and P <0.001, respectively). glycylphenylalanine 32-34 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 20672290-11 2011 The effect of LiCl on IL-6/IL-8/IL-10 secretion in iDC is mediated through inhibition of GSK-3beta. Lithium Chloride 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 21093446-5 2011 This yields wild-type 72aa IL-8 with a serine at its N-terminus. Serine 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 20472612-5 2011 High concentrations of hemin (50 muM) triggered TLR4-mediated IL-8 production in the human HEK293/TLR4 cell line in the absence of the co-receptors CD14 and MD-2; the latter an essential co-receptor for TLR4 activation by endotoxin. Hemin 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 20472612-7 2011 Coprohemin, in contrast to hemin, is unable to trigger TLR4-dependent activation of HEK/TLR4 cells, but instead causes dose-dependent inhibition of endotoxin-stimulated IL-8 production. coprohemin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 20472612-7 2011 Coprohemin, in contrast to hemin, is unable to trigger TLR4-dependent activation of HEK/TLR4 cells, but instead causes dose-dependent inhibition of endotoxin-stimulated IL-8 production. Hemin 5-10 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 20629184-7 2011 Curcumin significantly inhibited PMN chemotaxis against MIP-2, KC, or against conditioned media from LPS-treated macrophages or CEC, a well as the IL-8-mediated chemotaxis of human neutrophils. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 21175870-0 2011 Modulation of Interleukin-8 and staphylococcal flora by Avene hydrotherapy in patients suffering from chronic inflammatory dermatoses. avene 56-61 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 21175870-8 2011 Similarly, a significant decrease in PASI was associated with a significant reduction of IL-8, S. aureus colonization and enterotoxin N in patients with psoriasis. pasi 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 21221738-10 2011 F uptake was determined by difference from the original NaF concentration. Fluorine 0-1 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 21456255-1 2011 This work reports the corrosion behavior of nanotubular oxide layers on Ti-29Nb-xZr alloys with different compositions by anodization in 1 M H3PO4 + 0.8 wt% NaF. Oxides 56-61 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 20663020-8 2011 RESULTS: Pretreatment of PBMCs with alendronate promoted lipid A-induced production of IL-1beta and IL-6, but decreased lipid A-induced IL-8 and MCP-1 production. Alendronate 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 20663020-8 2011 RESULTS: Pretreatment of PBMCs with alendronate promoted lipid A-induced production of IL-1beta and IL-6, but decreased lipid A-induced IL-8 and MCP-1 production. Lipid A 120-127 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 20663020-9 2011 In human gingival fibroblasts, alendronate pretreatment increased lipid A-induced production of IL-6 and IL-8, and increased NF-kappaB activation in gingival fibroblasts but not PBMCs stimulated with lipid A. Alendronate 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 20663020-9 2011 In human gingival fibroblasts, alendronate pretreatment increased lipid A-induced production of IL-6 and IL-8, and increased NF-kappaB activation in gingival fibroblasts but not PBMCs stimulated with lipid A. Lipid A 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 20663020-11 2011 Finally, SIS3 inhibited alendronate-augmented IL-6 and IL-8 production by human gingival fibroblasts but up-regulated alendronate-decreased IL-8 production by PBMCs. Alendronate 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 20663020-11 2011 Finally, SIS3 inhibited alendronate-augmented IL-6 and IL-8 production by human gingival fibroblasts but up-regulated alendronate-decreased IL-8 production by PBMCs. Alendronate 118-129 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 21093446-7 2011 Interleukin-8 is purified via cation exchange chromatography and heparin affinity chromatography using a single inexpensive buffer system. Heparin 65-72 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 21241520-6 2011 RESULTS: There was a positive correlation between RDR to mannitol and eosinophil numbers (r = 0.47, p = 0.03) and level of IL-8 (r = 0.46, p = 0.04) in hypertonic saline-induced sputum. Sodium Chloride 163-169 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 20951221-10 2011 Capsazepine reduced dsRNA-induced IL-8 and it prevented dsRNA-induced loss of the NF-kappaB repressor protein IkBalpha. capsazepine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 21036957-9 2011 There was also an increase in interleukin-8 release by diatrizoate-treated cells indicating the possibility of proinflammatory effects of RCM. Diatrizoate 55-66 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 21175131-4 2011 Three triterpenic acids dose-dependently decreased production and expression of VEGF and IL-8, retained glutathione level, lowered ROS and NO levels, and declined cell invasion and migration in test cell lines (P < 0.05). triterpenic acids 6-23 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 20739465-10 2011 Hypertonicity-induced increases in IL-6 and IL-8 releases were suppressed by exposure to capsazepine, AG 1478, ERK inhibitor PD 98059, p38 inhibitor SB 203580, or NF-kappaB inhibitor PDTC. capsazepine 89-100 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 20739465-10 2011 Hypertonicity-induced increases in IL-6 and IL-8 releases were suppressed by exposure to capsazepine, AG 1478, ERK inhibitor PD 98059, p38 inhibitor SB 203580, or NF-kappaB inhibitor PDTC. RTKI cpd 102-109 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 20739465-10 2011 Hypertonicity-induced increases in IL-6 and IL-8 releases were suppressed by exposure to capsazepine, AG 1478, ERK inhibitor PD 98059, p38 inhibitor SB 203580, or NF-kappaB inhibitor PDTC. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 20739465-10 2011 Hypertonicity-induced increases in IL-6 and IL-8 releases were suppressed by exposure to capsazepine, AG 1478, ERK inhibitor PD 98059, p38 inhibitor SB 203580, or NF-kappaB inhibitor PDTC. SB 203580 149-158 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 24212612-7 2011 IL-8 production was stimulated by Lys8-psi-Lys9NT (8-13) and even enhanced at both acidic and alkaline pHe in BxPC-3 and PANC-1 cells. lys8-psi-lys9nt 34-49 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 20920494-5 2011 LPS-induced ICAM-1 and IL-8 expression was associated with increased superoxide formation in AEC. Superoxides 69-79 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 21062641-12 2011 In the presence of p38-MAPK and Syk inhibitors and monosodium urate crystals, IL-8 release was reduced. Uric Acid 51-67 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 21087659-5 2011 Also, exposure to HCHO for 30 min dose-dependently inhibited basal and lipopolysaccharide-induced interleukin-6 (IL-6) and IL-8 production by bronchial epithelial cells. Formaldehyde 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 24212612-7 2011 IL-8 production was stimulated by Lys8-psi-Lys9NT (8-13) and even enhanced at both acidic and alkaline pHe in BxPC-3 and PANC-1 cells. Phenylalanine 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 22110498-8 2011 Alveolar and plasma concentrations of IL-8 and TNF-alpha were significantly lower in the isoflurane group, whereas alveolar and plasma concentrations of MDA were significantly lower in the propofol group. Isoflurane 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 21809637-1 2011 People exposed to chronic influence of hydrogen sulphide gas demonstrate accelerated aging, increase of proinflammatory cytokine interleukin-8 level and the marker of apoptosis protein p53. Hydrogen Sulfide 39-56 C-X-C motif chemokine ligand 8 Homo sapiens 129-142 21711965-10 2011 Bay-117082 abolished hypoxia-stimulated IL-8 and VEGF synthesis, whereas Cyr61 restored the stimulative effect of hypoxia readily. 3-(4-methylphenylsulfonyl)-2-propenenitrile 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 21459369-6 2011 This response correlated with IL-8 but not TNFalpha or IL-6 production, and was abrogated by the NFkappaB inhibitor BAY 11-7082. 3-(4-methylphenylsulfonyl)-2-propenenitrile 116-127 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 21468920-0 2011 Polyozellin blocks tumor necrosis factor alpha-induced interleukin 8 and matrix metalloproteinase 7 production in the human intestinal epithelial cell line HT-29. polyozellin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 21468920-3 2011 Polyozellin significantly inhibited tumor necrosis factor (TNF)-alpha-induced interleukin-8 secretion and mRNA expression. polyozellin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 20844277-10 2011 The SIRT1 activators resveratrol and SRT1720 significantly decreased LPS-induced TNF, IL6, and IL8 gene expression and release and PTGS2 mRNA expression and resultant prostaglandin (PG) E(2) and PGF(2alpha) release from human gestational tissues. Resveratrol 21-32 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 20952496-7 2011 TTP binds to AU-rich elements in the 3"-UTR of the IL-8 mRNA. Gold 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 22040886-3 2011 We found that a potent androgen, 5alpha-dihydrotestosterone (DHT) inhibits IL-1alpha-induced production and mRNA expression of IL-8, IL-6 and IL-1beta from RA patient-derived fibroblast-like synovial cell line MH7A. Dihydrotestosterone 33-59 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 22040886-3 2011 We found that a potent androgen, 5alpha-dihydrotestosterone (DHT) inhibits IL-1alpha-induced production and mRNA expression of IL-8, IL-6 and IL-1beta from RA patient-derived fibroblast-like synovial cell line MH7A. Dihydrotestosterone 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 22040886-4 2011 Promoter analysis of the IL-8 gene revealed that nuclear factor (NF)-kappaB activation is critical for its transcriptional activation by IL-1alpha, and DHT inhibited the IL-1alpha-induced NF-kappaB activation in a manner dependent on the androgen receptor (AR). Dihydrotestosterone 152-155 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 21787693-4 2011 Nivalenol elicited interleukin (IL)-8 secretion. nivalenol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 19-37 21752354-3 2011 Stimulation of Fas induced the expression of pro-inflammatory mediators such as matrix metalloproteinase (MMP)-9 and IL-8. ammonium ferrous sulfate 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 21943646-5 2011 Here, we show that the effect of plasma membrane cholesterol depletion on the inhibition of Akt activation allows sustained ERK activation and the subsequent upregulation of IL-8 expression. Cholesterol 49-60 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 21787693-5 2011 IL-8 secretion was lower in cells concomitantly treated with nivalenol and NF-kappaB inhibitors than with nivalenol alone. nivalenol 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 21787693-5 2011 IL-8 secretion was lower in cells concomitantly treated with nivalenol and NF-kappaB inhibitors than with nivalenol alone. nivalenol 106-115 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 20950664-6 2011 CbpA could also induce the release of inflammatory cytokine interleukin-6, and chemokines CCL2, CXCL1, and CXCL8 from human bronchial epithelia cells. cbpa 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 107-112 21227887-7 2011 Tacrolimus was also demonstrated to down-regulate IFN-gamma-induced the secretion of chemotactic factor CXCL-8 and the expression of intercellular adhesion molecule-1 and human leucocyte antigen HLA-DR. Tacrolimus 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 104-110 20950664-8 2011 CbpA was also found to participate in the induction of IL-6, CCL2, CXCL1, and CXCL8 in the airways of mice upon intranasal challenge with S. pneumoniae. cbpa 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 20809700-0 2011 Evaluation of interleukin-8 in hepatitis C virus infection: relation to combined peg-interferon ribavirin response and genotype 4. Ribavirin 96-105 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 20809700-3 2011 The aim of the present study was to investigate the relationship among levels of IL-8 in serum of subjects with past exposure to HCV indicated by positive IgG to HCV and negative PCR, patients with chronic HCV infections and in responder to combined alfa IFN and ribavirin therapy. Ribavirin 263-272 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 21646801-10 2011 Budesonide significantly inhibited R-837-induced IL-8 production in a concentration-dependent manner, and procaterol potentiated inhibition by budesonide although single-agent procaterol had no effect. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 20809700-8 2011 The present study highlights the kinetic of serum levels of interleukin-8 in patients with chronic hepatitis C genotype 4 before and after therapy with combined alfa interferon and ribavirin. Ribavirin 181-190 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 20722064-5 2011 ATP increased flagellin-induced IL-8 secretion but reduced CCL20 secretion via distinct signaling pathways. Adenosine Triphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 20722064-6 2011 RESULTS: ATP-enhanced IL-8 production was only partly blocked by the P(2) receptor antagonist suramin and required activation of NF-kappaB while ATP-mediated reduction of CCL20 was completely blocked by suramin and required activation of ERK1/2. Adenosine Triphosphate 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 20722064-6 2011 RESULTS: ATP-enhanced IL-8 production was only partly blocked by the P(2) receptor antagonist suramin and required activation of NF-kappaB while ATP-mediated reduction of CCL20 was completely blocked by suramin and required activation of ERK1/2. Suramin 94-101 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 21646801-10 2011 Budesonide significantly inhibited R-837-induced IL-8 production in a concentration-dependent manner, and procaterol potentiated inhibition by budesonide although single-agent procaterol had no effect. Imiquimod 35-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 22003289-0 2011 Suppression of IL-8 production from airway cells by tiotropium bromide in vitro. Tiotropium Bromide 52-70 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 22003289-3 2011 PURPOSE: The present study aimed to examine the influence of tiotropium bromide on the production of interleukin (IL)-8 from human airway epithelial cells and lung fibroblasts (LFs) after lipopolysaccharide (LPS) stimulation in vitro. Tiotropium Bromide 61-79 C-X-C motif chemokine ligand 8 Homo sapiens 101-119 22003289-8 2011 RESULTS: Tiotropium bromide at > 15 pg/mL inhibited IL-8 production from both BEAS-2B cells and LFs after LPS stimulation. Tiotropium Bromide 9-27 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 22003289-9 2011 Tiotropium bromide also suppressed IL-8 mRNA expression through the inhibition of NF-kappaB activation and signaling protein, extracellular-signal-regulated kinase 1/2, and c-Jun N-terminal kinase, phosphorylation. Tiotropium Bromide 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 21496413-5 2011 In animal models and in vitro models, after treatment with Bosentan, a significant reduction of cytokine (TNF alpha, IFN gamma,IL-8, IL-4) levels was observed. Bosentan 59-67 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 22003289-10 2011 CONCLUSION: The present results strongly suggest that tiotropium bromide exerts the inhibitory effect on neutrophilic inflammation through the suppression of IL-8 production from epithelial cells and LFs by interfering with LPS-mediated signaling pathways and thus may contribute to lower cellular inflammation in COPD, which is responsible for favorable modification of the disease. Tiotropium Bromide 54-72 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 21496413-11 2011 Bosentan significantly reduced IL-2, IL-6, IL-8 and IFN- gamma levels in SSc patients, probably slowing progression to fibrosis and vascular damage. Bosentan 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 21224438-5 2011 The release of proinflammatory cytokines (tumor necrosis factor alpha, interleukin-6, and interleukin-8) was reduced by 1:1 and 1:2 DHA/AA ratios (P < .01 to P < .001) but increased by 1:4 and 1:7 DHA/AA ratios (P < .01 to P < .001) vs control. Docosahexaenoic Acids 132-135 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 22403987-11 2011 The positive control toothpaste containing 8.0% arginine and 1450 ppm fluoride as MFP in a calcium carbonate base provided statistically significant improvements in mean tactile and air blast dentin hypersensitivity scores compared to the negative control toothpaste containing 1100 ppm fluoride as NaF in a silica base (p < 0.05). Fluorides 70-78 C-X-C motif chemokine ligand 8 Homo sapiens 299-302 22403987-12 2011 The toothpaste containing 8.0% arginine and 1450 ppm fluoride as MFP in a calcium carbonate base (positive control) also provided statistically significant improvements in mean tactile and air blast dentin hypersensitivity scores compared to the test toothpaste containing 8% strontium acetate and 1040 ppm fluoride as NaF in a silica base. Fluorides 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 319-322 22403987-14 2011 CONCLUSION: The test toothpaste containing 8% strontium acetate and 1040 ppm fluoride as NaF in a silica base, when used for a single topical application and twice-daily brushing for seven days, does not provide statistically significant relief of dentin hypersensitivity compared to a negative control toothpaste containing 1100 ppm fluoride as NaF in a silica base. Fluorides 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 22403987-14 2011 CONCLUSION: The test toothpaste containing 8% strontium acetate and 1040 ppm fluoride as NaF in a silica base, when used for a single topical application and twice-daily brushing for seven days, does not provide statistically significant relief of dentin hypersensitivity compared to a negative control toothpaste containing 1100 ppm fluoride as NaF in a silica base. Silicon Dioxide 98-104 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 22403987-14 2011 CONCLUSION: The test toothpaste containing 8% strontium acetate and 1040 ppm fluoride as NaF in a silica base, when used for a single topical application and twice-daily brushing for seven days, does not provide statistically significant relief of dentin hypersensitivity compared to a negative control toothpaste containing 1100 ppm fluoride as NaF in a silica base. silica base 98-109 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 20882041-4 2011 In particular, IL-8, urokinase-like plasminogen activator receptor, and metalloproteinases are highly upregulated after cholesterol extraction. Cholesterol 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 15-66 21099203-6 2011 M-TriDAP induced a dose-dependent release of IL-8, MIP-1alpha, MIP-1beta and TNF. L-Ala-gamma-D-Glu-meso-diaminopimelic acid 2-8 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 20382011-4 2011 We found that GPE attenuated TNFalpha-induced expression of inflammatory genes including interleukin (IL)-6, IL-1beta, IL-8, monocyte chemoattractant protein (MCP)-1, cyclooxygenase (COX)-2 and Toll-like receptor (TLR)-2. gpe 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 20594065-2 2011 Fluoridated HA (fluorapatite) was prepared by reacting resorbable synthetic HA (OsteoGen, Impladent, Ltd, Holliswood, NY) with 4.3% sodium fluoride (NaF) for 2 minutes. fluorapatite 16-28 C-X-C motif chemokine ligand 8 Homo sapiens 149-152 21992563-6 2011 However, an in vivo neutrophil migration assay following 5d-FRH and during the post-exposure recovery period also showed persistently enhanced neutrophil influx in response to a fixed chemotactic gradient generated by recombinant human IL-8, suggesting that additional mechanisms besides increased ELR + CXC chemokines contributed to the augmented neutrophil response caused by 5d-FRH exposure. 5d-frh 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 21992563-6 2011 However, an in vivo neutrophil migration assay following 5d-FRH and during the post-exposure recovery period also showed persistently enhanced neutrophil influx in response to a fixed chemotactic gradient generated by recombinant human IL-8, suggesting that additional mechanisms besides increased ELR + CXC chemokines contributed to the augmented neutrophil response caused by 5d-FRH exposure. 5d-frh 378-384 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 22121382-8 2011 Salmeterol increased, while dexamethasone and fluticasone decreased RV-induced IL-6 and IL-8 (P<0.05). Dexamethasone 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 22121382-8 2011 Salmeterol increased, while dexamethasone and fluticasone decreased RV-induced IL-6 and IL-8 (P<0.05). Fluticasone 46-57 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 22403977-14 2011 CONCLUSION: The results of this double-blind clinical study support that 1) an alcohol-free mouthwash containing a combination of 0.075% CPC and 0.05% NaF produces statistically significant reductions in dental plaque and gingivitis after three and six months compared to baseline, and 2) the alcohol-free CPC mouthwash provides a statistically significantly greater level of efficacy in controlling established dental plaque and gingivitis after three and six months of product use as compared to the Control Mouthwash containing only NaF. Alcohols 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 22403977-14 2011 CONCLUSION: The results of this double-blind clinical study support that 1) an alcohol-free mouthwash containing a combination of 0.075% CPC and 0.05% NaF produces statistically significant reductions in dental plaque and gingivitis after three and six months compared to baseline, and 2) the alcohol-free CPC mouthwash provides a statistically significantly greater level of efficacy in controlling established dental plaque and gingivitis after three and six months of product use as compared to the Control Mouthwash containing only NaF. Alcohols 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 536-539 22403977-14 2011 CONCLUSION: The results of this double-blind clinical study support that 1) an alcohol-free mouthwash containing a combination of 0.075% CPC and 0.05% NaF produces statistically significant reductions in dental plaque and gingivitis after three and six months compared to baseline, and 2) the alcohol-free CPC mouthwash provides a statistically significantly greater level of efficacy in controlling established dental plaque and gingivitis after three and six months of product use as compared to the Control Mouthwash containing only NaF. Cetylpyridinium 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 536-539 22403977-14 2011 CONCLUSION: The results of this double-blind clinical study support that 1) an alcohol-free mouthwash containing a combination of 0.075% CPC and 0.05% NaF produces statistically significant reductions in dental plaque and gingivitis after three and six months compared to baseline, and 2) the alcohol-free CPC mouthwash provides a statistically significantly greater level of efficacy in controlling established dental plaque and gingivitis after three and six months of product use as compared to the Control Mouthwash containing only NaF. Alcohols 293-300 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 22403977-14 2011 CONCLUSION: The results of this double-blind clinical study support that 1) an alcohol-free mouthwash containing a combination of 0.075% CPC and 0.05% NaF produces statistically significant reductions in dental plaque and gingivitis after three and six months compared to baseline, and 2) the alcohol-free CPC mouthwash provides a statistically significantly greater level of efficacy in controlling established dental plaque and gingivitis after three and six months of product use as compared to the Control Mouthwash containing only NaF. Cetylpyridinium 306-309 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 20454998-6 2011 Conversely, enforced expression of CypA in the CypA KD cell line, Ud-12, markedly enhanced IL-8 transcripts and restored Ud-12 proliferation, suggesting that CypA-mediated IL-8 production provides a growth advantage to glioblastoma cells. UD 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 20454998-6 2011 Conversely, enforced expression of CypA in the CypA KD cell line, Ud-12, markedly enhanced IL-8 transcripts and restored Ud-12 proliferation, suggesting that CypA-mediated IL-8 production provides a growth advantage to glioblastoma cells. UD 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 21908944-0 2011 beta-Carotene and lutein inhibit hydrogen peroxide-induced activation of NF-kappaB and IL-8 expression in gastric epithelial AGS cells. beta Carotene 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 21908944-0 2011 beta-Carotene and lutein inhibit hydrogen peroxide-induced activation of NF-kappaB and IL-8 expression in gastric epithelial AGS cells. Hydrogen Peroxide 33-50 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 21908944-7 2011 The present study aims to investigate whether beta-carotene and lutein inhibit H(2)O(2)-induced activation of NF-kappaB and expression of IL-8 in gastric epithelial AGS cells. beta Carotene 46-59 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 21908944-7 2011 The present study aims to investigate whether beta-carotene and lutein inhibit H(2)O(2)-induced activation of NF-kappaB and expression of IL-8 in gastric epithelial AGS cells. Hydrogen Peroxide 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 21908944-13 2011 As a result, H(2)O(2 )induced the activation of NF-kappaB and expression of IL-8 in AGS cells time-dependently. Hydrogen Peroxide 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 21908944-14 2011 beta-Carotene and lutein showed inhibitory effects on H(2)O(2)-induced increase in intracellular ROS levels, activation of NF-kappaB, and IL-8 expression in AGS cells. beta Carotene 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 21908944-14 2011 beta-Carotene and lutein showed inhibitory effects on H(2)O(2)-induced increase in intracellular ROS levels, activation of NF-kappaB, and IL-8 expression in AGS cells. Hydrogen Peroxide 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 22470793-0 2011 Particle disease on fluoride-18 (NaF) PET/CT imaging. fluoride-18 20-31 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 22531121-7 2011 The concentrations of IL-6, IL-8, VEGF and MMP-2 protein in the culture supernatant of MKN-45P were significantly higher than those of MKN-45. mkn-45p 87-94 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 22531121-7 2011 The concentrations of IL-6, IL-8, VEGF and MMP-2 protein in the culture supernatant of MKN-45P were significantly higher than those of MKN-45. mkn-45 87-93 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 21954641-1 2011 The use of metformin during the first month of treatment of patients with coronary artery disease and diabetes type 2 led to the decrease of insulin resistance and reduced activity of systemic inflammation (significant decrease in the concentrations of IL-1, IL-6, IL-8 and TNF-alpha). Metformin 11-20 C-X-C motif chemokine ligand 8 Homo sapiens 265-269 21938919-1 2011 The authors revealed increase in ageing pace, higher level of pro-inflammatory cytokine Interleukin-8 and apoptosis marker (p53 protein) in individuals with chronic exposure to gas containing hydrogen sulfide. Hydrogen Sulfide 192-208 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 21765616-0 2011 Modulation of NK cell autocrine-induced eosinophil chemotaxis by interleukin-15 and vitamin D(3): a possible NK-eosinophil crosstalk via IL-8 in the pathophysiology of allergic rhinitis. Vitamin D 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 21765616-5 2011 The amount of IL-8 secreted by NK cells was increased by IL-15 treatment from levels of 88.64 +- 21.5 to 178.9 +- 23.6 Pg/mL and was significantly reduced by 10(-6) M vitamin D(3) to levels of 59.2 +- 16.3 Pg/mL. Vitamin D 167-176 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 21112343-9 2011 Using inhibitor SN50, palmitate-induced expression of IL8, CXCL3 and CCL20 was NFkappaB-dependent (all p<0.05). Palmitates 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 21765616-6 2011 Our results indicate a novel inflammatory crosstalk between NK cells and eosinophils via IL-15/IL-8 axis that can be modulated by vitamin D(3). Vitamin D 130-139 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 21057930-2 2011 The output of an ELISpot assay is a formation of colored spots which appear at the sites of cells releasing cytokines, with each individual spot representing a single cytokine-releasing cell.We have shown that hydrogen peroxide-induced oxidative stress was causing ~twofold decrease in the number of lymphocytes secreting the TH1 cytokines IFN-gamma and IL-2, as well as chemokine IL-8 and cytokine TNF alpha. Hydrogen Peroxide 210-227 C-X-C motif chemokine ligand 8 Homo sapiens 381-385 21057930-5 2011 We adopted ELISpot assay for studying oxidative stress in human peripheral blood lymphocytes by analyzing the acute effect of hydrogen peroxide treatment on the frequency of cells secreting IFN-gamma, IL-2, IL-4, IL-5, IL-8, and TNF-alpha. Hydrogen Peroxide 126-143 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 21112343-10 2011 Furthermore, JNK was involved in palmitate-induced expression of IL1A, IL8, CXCL3, SPP1 and CEBPB as determined with inhibitor SP600125 (all p<0.05). Palmitates 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 21269946-7 2011 ADMA treatment also resulted in a dose-dependent increase of the levels of TNF-alpha and IL-8 in the culture supernatant of the macrophages, and the peak levels occurred following the treatment with 15 micromol/L ADMA. N,N-dimethylarginine 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 22171160-7 2011 RESULTS: Capsaicin (CAP; a selective TRPV1 agonist), induced time-dependent activation of transforming growth factor-activated kinase 1 (TAK1) and mitogen-activated protein kinase (MAPK) cascades temporally followed by increased nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha (IkappaBalpha) phosphorylation, rises in both PKCdelta protein levels and IL-6 and IL-8 release. Capsaicin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 396-400 22171160-7 2011 RESULTS: Capsaicin (CAP; a selective TRPV1 agonist), induced time-dependent activation of transforming growth factor-activated kinase 1 (TAK1) and mitogen-activated protein kinase (MAPK) cascades temporally followed by increased nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha (IkappaBalpha) phosphorylation, rises in both PKCdelta protein levels and IL-6 and IL-8 release. Capsaicin 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 396-400 22194647-13 2011 Mapracorat inhibited eosinophil migration and IL-8 release from eosinophils or the release of IL-6, IL-8, CCL5/RANTES, and TNF-alpha from a human mast cell line with equal potency as dexamethasone, whereas it was clearly less potent than this glucocorticoid in inducing annexin I and CXCR4 expression on the human eosinophil surface; this was taken as a possible sign of glucocorticoid-dependent transactivation. R-1,1,1-trifluoro-4-(5-fluoro-2,3-dihydrobenzofuran-7-yl)-4-methyl-2-(((2-methyl-5-quinolyl)amino)methyl)pentan-2-ol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 22194647-13 2011 Mapracorat inhibited eosinophil migration and IL-8 release from eosinophils or the release of IL-6, IL-8, CCL5/RANTES, and TNF-alpha from a human mast cell line with equal potency as dexamethasone, whereas it was clearly less potent than this glucocorticoid in inducing annexin I and CXCR4 expression on the human eosinophil surface; this was taken as a possible sign of glucocorticoid-dependent transactivation. R-1,1,1-trifluoro-4-(5-fluoro-2,3-dihydrobenzofuran-7-yl)-4-methyl-2-(((2-methyl-5-quinolyl)amino)methyl)pentan-2-ol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 22219634-9 2011 The result of ELISA also showed that the release of IL-6 and IL-8 can be inhibited by high glucose, but these inhibitions were partly counteracted after pretreatment with anti-TLR2 and/or anti-TLR4 monoclonal antibody. Glucose 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 21269946-7 2011 ADMA treatment also resulted in a dose-dependent increase of the levels of TNF-alpha and IL-8 in the culture supernatant of the macrophages, and the peak levels occurred following the treatment with 15 micromol/L ADMA. N,N-dimethylarginine 213-217 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 21269946-8 2011 CONCLUSION: ADMA can up-regulate MIF expression and induce TNF-alpha and IL-8 secretion in THP-1 monocyte-derived macrophages. N,N-dimethylarginine 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 21462088-6 2011 The molecular mechanism of garcinol"s action on PaCa cells was investigated by targeting signaling moieties involved in apoptosis (X-IAP, cIAP, caspase-3, 9, and PARP cleavage), transcription factor NF-kappaB, believed to contribute toward a chemoresistance phenotype in pancreatic tumors, and molecules associated with neovascularization and metastasis (MMP-9, VEGF, IL-8, and PGE(2)). garcinol 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 368-372 20571097-8 2011 This could be confirmed ex vivo, as the prevalence of non-epitheloid phenotype of MC in the standard group was significantly higher with increasing PD duration and MC isolated from this group showed significantly higher levels of EMT-associated molecules including fibronectin, collagen I, VEGF, IL-8 and TGF-beta levels when compared with the low-GDP group. Methylcholanthrene 164-166 C-X-C motif chemokine ligand 8 Homo sapiens 296-300 20571097-10 2011 In addition, the levels of EMT-associated molecules (fibronectin, VEGF and IL-8) increased in the standard but decreased in the low-GDP group. Guanosine Diphosphate 132-135 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 20571097-12 2011 Accordingly, effluent MC with non-epitheloid morphology showed significantly lower levels of E-cadherin and greater levels of fibronectin, collagen I, VEGF and IL 8 when compared with MC with epitheloid phenotype. Methylcholanthrene 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 21935477-10 2011 Microarray analysis of islets exposed to Imatinib for 4 hours revealed increased expression of the inflammatory genes IL-4R, TCF5, DR5, I-TRAF, I-CAM, HSP27 and IL-8. Imatinib Mesylate 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 22194966-2 2011 This posttranslational modification of arginine was recently discovered on inflammatory chemokines including CXCL8 and CXCL10, and significantly reduced their biological activity. Arginine 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 109-114 22039452-3 2011 Quercetin significantly attenuated intercellular adhesion molecule-1 (ICAM-1), interleukin (IL) -6, IL-8, and cyclooxygenase (COX) -2 mRNA expression, and inhibited IL-1beta-induced increases in ICAM-1, IL-6, and IL-8 mRNA. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 22039452-3 2011 Quercetin significantly attenuated intercellular adhesion molecule-1 (ICAM-1), interleukin (IL) -6, IL-8, and cyclooxygenase (COX) -2 mRNA expression, and inhibited IL-1beta-induced increases in ICAM-1, IL-6, and IL-8 mRNA. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 21594207-9 2011 Only one product with NaF as fluoride supplement showed both total and free fluoride concentrations above 1,000 ppm F-. Fluorides 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 21594207-9 2011 Only one product with NaF as fluoride supplement showed both total and free fluoride concentrations above 1,000 ppm F-. Fluorides 76-84 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 21757966-6 2011 CAM treatment was more effective for IL-8(high) CRSnNP patients than for IL-8(low) CRSnNP patients (p < 0.05). Clarithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 21757966-6 2011 CAM treatment was more effective for IL-8(high) CRSnNP patients than for IL-8(low) CRSnNP patients (p < 0.05). Clarithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 22216191-0 2011 Mycobacterium abscessus glycopeptidolipid prevents respiratory epithelial TLR2 signaling as measured by HbetaD2 gene expression and IL-8 release. glycopeptidolipid 24-41 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 22205926-3 2011 METHODOLOGY/PRINCIPAL FINDINGS: Corticosteroid sensitivity was determined by the dexamethasone ability to inhibit TNFalpha-induced IL-8 or LPS-induced TNFalpha production. Dexamethasone 81-94 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 21935477-11 2011 The islet release of IL-8 was augmented in islets cultured over night in the presence of Imatinib. Imatinib Mesylate 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 21904597-8 2011 The truncated forms CXCL8(2-77) and CXCL8(3-77) had higher affinity for heparin than CXCL8(1-77), a property important for the presentation of CXCL8 on endothelial layers. Heparin 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 20-25 21904597-8 2011 The truncated forms CXCL8(2-77) and CXCL8(3-77) had higher affinity for heparin than CXCL8(1-77), a property important for the presentation of CXCL8 on endothelial layers. Heparin 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 21904597-8 2011 The truncated forms CXCL8(2-77) and CXCL8(3-77) had higher affinity for heparin than CXCL8(1-77), a property important for the presentation of CXCL8 on endothelial layers. Heparin 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 21904597-8 2011 The truncated forms CXCL8(2-77) and CXCL8(3-77) had higher affinity for heparin than CXCL8(1-77), a property important for the presentation of CXCL8 on endothelial layers. Heparin 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 21738617-6 2011 Exposure of BMCs to CSE induced IL-8 and TGF-beta1 production, which was dependent on NF-kappaB and ERK1/2, but not on AKT. bmcs 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 21826199-0 2011 Anti-inflammatory effect of fluvastatin on IL-8 production induced by Pseudomonas aeruginosa and Aspergillus fumigatus antigens in cystic fibrosis. Fluvastatin 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 21826199-2 2011 Since recent research has identified the anti-inflammatory properties of statins (besides their lipid-lowering effects), we investigated the effect of fluvastatin on the production of the potent neutrophil chemoattractant chemokine, IL-8, in whole blood from CF patients, stimulated by Pseudomonas aeruginosa (LPS) and Aspergillus fumigatus (AFA) antigens. Fluvastatin 151-162 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 21826199-6 2011 Fluvastatin strongly decreased the levels of IL-8, in a concentration-dependent manner, in whole blood from CF patients. Fluvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 21633494-7 2011 We show that STBM can bind to monocytes and B cells and induce cytokine release (TNFalpha, MIP-1alpha, IL-1alpha, IL-1beta, IL-6, IL-8). stbm 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 21625550-0 2011 Lycopene inhibits NF-kB-mediated IL-8 expression and changes redox and PPARgamma signalling in cigarette smoke-stimulated macrophages. Lycopene 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 21625550-3 2011 The aim of this study was to investigate the role of lycopene on the production of the pro-inflammatory cytokine IL-8 induced by cigarette smoke and the possible mechanisms implicated. Lycopene 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 21625550-6 2011 Lycopene pre-treatment resulted in a significant inhibition of CSE-induced IL-8 expression at both mRNA and protein levels. Lycopene 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 21625550-13 2011 Taken together, our data indicate that lycopene prevented CSE-induced IL-8 production through a mechanism involving an inactivation of NF-kB. Lycopene 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 21625550-15 2011 The ability of lycopene in inhibiting IL-8 production, NF-kB/p65 nuclear translocation, and redox signalling and in increasing PPARgamma expression was also found in isolated rat alveolar macrophages exposed to CSE. Lycopene 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 21779360-4 2011 Our findings showed that pretreatment of HaCaT cells with NaHS (a donor of H(2)S) for 30 min before exposure to CoCl(2) for 24 h significantly attenuated CoCl(2)-induced injuries and inflammatory responses, evidenced by increases in cell viability and GSH level and decreases in ROS generation and secretions of IL-1beta, IL-6 and IL-8. sodium bisulfide 58-62 C-X-C motif chemokine ligand 8 Homo sapiens 331-335 21779360-4 2011 Our findings showed that pretreatment of HaCaT cells with NaHS (a donor of H(2)S) for 30 min before exposure to CoCl(2) for 24 h significantly attenuated CoCl(2)-induced injuries and inflammatory responses, evidenced by increases in cell viability and GSH level and decreases in ROS generation and secretions of IL-1beta, IL-6 and IL-8. Hydrogen Sulfide 75-80 C-X-C motif chemokine ligand 8 Homo sapiens 331-335 21779360-6 2011 Similar to the protective effect of H(2)S, both NS-398 (a selective COX-2 inhibitor) and PDTC (a selective NF-kappaB inhibitor) depressed not only CoCl(2)-induced cytotoxicity, but also the secretions of IL-1beta, IL-6 and IL-8. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 48-54 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 21822181-7 2011 There was a significant negative correlation between levels of IL-8 and pH (r=-0.83, p<0.05), and of IL-8 and glucose in pleural fluid (r=-0.61, p<0.05). Glucose 113-120 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 20932985-0 2011 Poly(I:C) reduces expression of JAM-A and induces secretion of IL-8 and TNF-alpha via distinct NF-kappaB pathways in human nasal epithelial cells. poly 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 20932985-0 2011 Poly(I:C) reduces expression of JAM-A and induces secretion of IL-8 and TNF-alpha via distinct NF-kappaB pathways in human nasal epithelial cells. Iodine 5-6 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 20932985-0 2011 Poly(I:C) reduces expression of JAM-A and induces secretion of IL-8 and TNF-alpha via distinct NF-kappaB pathways in human nasal epithelial cells. Carbon 7-8 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 20932985-5 2011 In hTERT-transfected HNECs, treatment with poly(I:C) significantly reduced expression of the tight junction protein JAM-A and induced secretion of proinflammatory cytokines IL-8 and TNF-alpha. Poly I-C 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 20932985-6 2011 Both the reduction of JAM-A expression and the induction of secretion of IL-8 and TNF-alpha after treatment with poly(I:C) were modulated by distinct signal transduction pathways via EGFR, PI3K, and p38 MAPK and finally regulated by a TLR3-mediated NF-kappaB pathway. poly 113-117 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 20932985-6 2011 Both the reduction of JAM-A expression and the induction of secretion of IL-8 and TNF-alpha after treatment with poly(I:C) were modulated by distinct signal transduction pathways via EGFR, PI3K, and p38 MAPK and finally regulated by a TLR3-mediated NF-kappaB pathway. Carbon 120-121 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 25214996-16 2011 The level of serum IL-8 was positively correlated with white blood cell count and ISS score, and inversely correlated with oxygen index. Oxygen 123-129 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 20615393-0 2010 Decoy oligodeoxyribonucleotides and peptide nucleic acids-DNA chimeras targeting nuclear factor kappa-B: inhibition of IL-8 gene expression in cystic fibrosis cells infected with Pseudomonas aeruginosa. Oligodeoxyribonucleotides 6-31 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 20615393-5 2010 Here, we review the inhibitory effects of decoy oligodeoxyribonucleotides (ODNs) on expression of IL-8 gene and secretion of IL-8 by cystic fibrosis cells infected by Pseudomonas aeruginosa. decoy oligodeoxyribonucleotides 42-73 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 20615393-5 2010 Here, we review the inhibitory effects of decoy oligodeoxyribonucleotides (ODNs) on expression of IL-8 gene and secretion of IL-8 by cystic fibrosis cells infected by Pseudomonas aeruginosa. decoy oligodeoxyribonucleotides 42-73 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 20816778-9 2010 50% of the control, whereas EGCG provoked a decrease in the IL-6 and IL-8 over-secretion, by 50 and 60%, respectively. epigallocatechin gallate 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 21162728-10 2010 A CYP1A1 inhibitor (alpha-naphthoflavone), nearly abolished the DEP-induced expression of IL-8 and COX-2. alpha-naphthoflavone 20-40 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 21162728-12 2010 A p38 inhibitor (SB202190) strongly reduced DEP-induced expression of IL-6, IL-8 and COX-2, but only moderately affected the expression of CYP1A1. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 20923702-2 2010 This report concerns the strong proinflammatory action that a dietary oxysterol mixture and, to a lesser extent, an identical concentration of unoxidized cholesterol exert on CaCo-2 colonic epithelial cells by up-regulating both expression and synthesis of interleukin 8. Oxysterols 70-79 C-X-C motif chemokine ligand 8 Homo sapiens 257-270 20943792-7 2010 RESULTS: Quercetin, and to a lesser extent trans-RSV, attenuated the TNF-alpha-induced expression of inflammatory genes such as interleukin (IL)-6, IL-1beta, IL-8, and monocyte chemoattractant protein-1 (MCP-1) and the secretion of IL-6, IL-8, and MCP-1. Quercetin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 20943792-7 2010 RESULTS: Quercetin, and to a lesser extent trans-RSV, attenuated the TNF-alpha-induced expression of inflammatory genes such as interleukin (IL)-6, IL-1beta, IL-8, and monocyte chemoattractant protein-1 (MCP-1) and the secretion of IL-6, IL-8, and MCP-1. Resveratrol 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 20943792-7 2010 RESULTS: Quercetin, and to a lesser extent trans-RSV, attenuated the TNF-alpha-induced expression of inflammatory genes such as interleukin (IL)-6, IL-1beta, IL-8, and monocyte chemoattractant protein-1 (MCP-1) and the secretion of IL-6, IL-8, and MCP-1. Quercetin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 20889674-3 2010 We particularly focused on the effects of LTD4 on release of heparin-binding EGF-like factor (HB-EGF) and IL-8 (CXCL8), a potent neutrophil chemoattractant that may be released downstream of EGFR activation. Leukotriene D4 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 20729385-7 2010 Pretreatment with budesonide, a currently used inhaled corticosteroid, decreased LPS-induced expression of TNF-alpha, IL-6, and IL-8, and reduced LPS-induced neutrophilia by ~84%. Budesonide 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 20889674-3 2010 We particularly focused on the effects of LTD4 on release of heparin-binding EGF-like factor (HB-EGF) and IL-8 (CXCL8), a potent neutrophil chemoattractant that may be released downstream of EGFR activation. Leukotriene D4 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 112-117 20049553-3 2010 Here, we demonstrated that middle (1.0 mmol/L) and high (10.0 mmol/L) concentrations of sodium fluoride (NaF) significantly inhibited hair follicle elongation in vitro, but low NaF (0.1 mmol/L) showed little influence. Sodium Fluoride 88-103 C-X-C motif chemokine ligand 8 Homo sapiens 105-108 20049553-4 2010 Moreover, treatment with high levels of NaF resulted in a marked increase in terminal dUTP nick end labeling-positive cells in the outer layer of the outer root sheath, the dermal sheath, and the lower bulb matrix surrounding dermal papilla. deoxyuridine triphosphate 86-90 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 20049553-6 2010 Additionally, the presence of selenium considerably antagonized the effects of middle NaF on hair follicles, with regard to either the suppression of hair growth or the induction of oxidative stress and apoptosis. Selenium 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 21169142-11 2010 Release of C3a was attenuated in the fenoldopam group (P = .002), and release of IL-6 and IL-8 was attenuated in the postoperative period in the fenoldopam group (P = .012 and .015, respectively). Fenoldopam 145-155 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 20198424-10 2010 IL-8 mRNA expression in the esophageal mucosa of patients with rebamipide was significantly decreased compared with that of patients without rebamipide. rebamipide 63-73 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 20198424-10 2010 IL-8 mRNA expression in the esophageal mucosa of patients with rebamipide was significantly decreased compared with that of patients without rebamipide. rebamipide 141-151 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 20826566-10 2010 Furthermore, dexamethasone-enhanced ATP induction of adhesion molecule transcription and augmented the release of IL-8. Dexamethasone 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 20384691-0 2010 Influence of high dose tumescent local anaesthesia with prilocaine on systemic interleukin (IL)-6, IL-8 and tumour necrosis factor-alpha. Prilocaine 56-66 C-X-C motif chemokine ligand 8 Homo sapiens 99-136 20607584-0 2010 Rebamipide inhibits tumor necrosis factor-alpha-induced interleukin-8 expression by suppressing the NF-kappaB signal pathway in human umbilical vein endothelial cells. rebamipide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 20607584-1 2010 OBJECTIVE: This study was designed to identify the inhibitory effect of rebamipide on tumor necrosis factor-alpha (TNF-alpha)-induced interleukin-8 (IL-8) production and nuclear factor-kappaB (NF-kappaB) activation in human umbilical vein endothelial cells (HUVECs). rebamipide 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 134-147 20607584-1 2010 OBJECTIVE: This study was designed to identify the inhibitory effect of rebamipide on tumor necrosis factor-alpha (TNF-alpha)-induced interleukin-8 (IL-8) production and nuclear factor-kappaB (NF-kappaB) activation in human umbilical vein endothelial cells (HUVECs). rebamipide 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 20607584-6 2010 RESULTS: We found that rebamipide decreased the expression of IL-8 in the dose-dependent manner under the treatment with TNF-alpha 10 ng/ml. rebamipide 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 20607584-9 2010 CONCLUSION: Rebamipide suppresses TNF-alpha-induced IL-8 production through (1) inhibition of IkappaB-alpha phosphorylation in the cytoplasm and (2) blockage of NF-kappaB p65 protein transport into the nucleus. rebamipide 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 20607584-10 2010 We suggest that the anti-inflammatory effect of rebamipide is related to the down-regulation of IL-8 expression that is important in endothelial inflammation. rebamipide 48-58 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 20976506-0 2010 Suppressive effects of sivelestat on interleukin 8 and TNF-alpha production from LPS-stimulated granulocytes in whole blood culture. sivelestat 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 20976506-9 2010 CONCLUSION: Suppression of granulocytic production of IL-8 and TNF-alpha by sivelestat suggests that this drug may be useful for treatment of morbid conditions involving IL-8 and TNF-alpha at onset. sivelestat 76-86 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 20976506-9 2010 CONCLUSION: Suppression of granulocytic production of IL-8 and TNF-alpha by sivelestat suggests that this drug may be useful for treatment of morbid conditions involving IL-8 and TNF-alpha at onset. sivelestat 76-86 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 20801891-8 2010 Dexamethasone and resveratrol inhibited concentration-dependently TNFalpha-induced IL-8, GM-CSF, and VEGF release. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 20801891-8 2010 Dexamethasone and resveratrol inhibited concentration-dependently TNFalpha-induced IL-8, GM-CSF, and VEGF release. Resveratrol 18-29 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 20801891-9 2010 For IL-8 and GM-CSF efficiency of dexamethasone was NS > S > COPD. Dexamethasone 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 20801891-10 2010 That of resveratrol was NS = S = COPD for IL-8 and NS = S < COPD for GM-CSF. Resveratrol 8-19 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 21179282-8 2010 Treatment with inhibitors of nuclear factor-kappaB (NF-kappaB), i.e., pyrrolidine dithiocarbamate and parthenolide, abrogated the stimulatory effect of poly (I:C) on the production of VEGF and IL-8 in RA FLS. pyrrolidine dithiocarbamic acid 70-97 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 21179282-8 2010 Treatment with inhibitors of nuclear factor-kappaB (NF-kappaB), i.e., pyrrolidine dithiocarbamate and parthenolide, abrogated the stimulatory effect of poly (I:C) on the production of VEGF and IL-8 in RA FLS. parthenolide 102-114 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 20725767-5 2010 NaF treatment, which increased the rate of apoptosis in a time- and dose-dependent manner, also increased the levels of inositol mono- and bis-phosphates and drastically reduced the levels of inositol tris- and tetrakis-phosphates. inositol mono- and bis-phosphates 120-153 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 20725767-5 2010 NaF treatment, which increased the rate of apoptosis in a time- and dose-dependent manner, also increased the levels of inositol mono- and bis-phosphates and drastically reduced the levels of inositol tris- and tetrakis-phosphates. inositol tris- and tetrakis-phosphates 192-230 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 20725767-6 2010 Prior treatment with antimycin A, a strategy used to reverse the NaF-induced accumulations of higher InsPs, partially reduced the effects of NaF on apoptosis as well as the levels of lower InsPs. Antimycin A 21-32 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 20725767-6 2010 Prior treatment with antimycin A, a strategy used to reverse the NaF-induced accumulations of higher InsPs, partially reduced the effects of NaF on apoptosis as well as the levels of lower InsPs. Antimycin A 21-32 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 20657019-1 2010 BACKGROUND: The authors previously reported that human ocular surface epithelium expressed TLR3 and that its ligand polyI:C stimulated the secretion of IL-6, IL-8 and IFN-beta. Poly I-C 116-123 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 21442075-0 2010 Dexamethasone-induced apoptosis of freshly isolated human nasal epithelial cells concomitant with abrogation of IL-8 production. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 21442075-11 2010 Dexamethasone induced apoptosis of hNECs concomitant with abrogation of IL-8 production by hNECs. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 21442075-13 2010 Dexamethasone induces apoptosis of hNECs and abrogates IL-8 production. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 20677965-7 2010 RESULTS: Only coated samples with the highest fluoride content (group D, 0.4 g of NaF) were able to release fluoride at therapeutic levels. Fluorides 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 20677965-8 2010 When fluoride release from coated and uncoated samples with the same amount of NaF were compared, it was shown that the dip-coating technique resulted in a fluoride release in a controlled manner while eliminating the initial burst effect. 3,5-diisopropylsalicylic acid 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 20600865-5 2010 In the present study, we show that exposure of endothelial cells to low magnesium increases the secretion of RANTES, interleukin 8 and platelet derived growth factor BB, all important players in atherogenesis. Magnesium 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 20826776-4 2010 Norepinephrine (NE) treatment of ovarian cancer cells resulted in a 250-300% increase in IL8 protein and 240-320% increase in its mRNA levels. Norepinephrine 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 20826776-8 2010 Promoter deletion analyses suggested that AP1 transcription factors might mediate catecholamine-stimulated up-regulation of IL8. Catecholamines 82-95 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 20826776-11 2010 This enhanced tumor growth was completely blocked by IL8 or FosB gene silencing using 1,2-dioleoyl-sn-glycero-3-phosphatidylcholine nanoliposomes. 1,2-oleoylphosphatidylcholine 86-131 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 20632048-0 2010 Nickel induces oxidative burst, NF-kappaB activation and interleukin-8 production in human neutrophils. Nickel 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 20949640-10 2010 Human islets also responded to beta-GalCer (10 microg/mL) by secreting TNFalpha, IL-1beta and IL-8, whereas sulfatide partly inhibited the effect of LPS. beta-GalCer 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 20518825-3 2010 In this study, we investigated the effects of interleukin-8 (IL-8), a known neutrophil chemoattractant, on lipopolysaccharide (LPS) -induced reactive oxygen species (ROS) production by endothelial cells, and its significance in the pathogenesis of LPS-mediated sepsis. Reactive Oxygen Species 141-164 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 20518825-3 2010 In this study, we investigated the effects of interleukin-8 (IL-8), a known neutrophil chemoattractant, on lipopolysaccharide (LPS) -induced reactive oxygen species (ROS) production by endothelial cells, and its significance in the pathogenesis of LPS-mediated sepsis. Reactive Oxygen Species 141-164 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 20518825-3 2010 In this study, we investigated the effects of interleukin-8 (IL-8), a known neutrophil chemoattractant, on lipopolysaccharide (LPS) -induced reactive oxygen species (ROS) production by endothelial cells, and its significance in the pathogenesis of LPS-mediated sepsis. Reactive Oxygen Species 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 20518825-3 2010 In this study, we investigated the effects of interleukin-8 (IL-8), a known neutrophil chemoattractant, on lipopolysaccharide (LPS) -induced reactive oxygen species (ROS) production by endothelial cells, and its significance in the pathogenesis of LPS-mediated sepsis. Reactive Oxygen Species 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 20518825-4 2010 The results revealed that IL-8 directly induced ROS production in human umbilical vein endothelial cells (HUVECs), and also mediated LPS-induced ROS production by HUVECs. Reactive Oxygen Species 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20518825-4 2010 The results revealed that IL-8 directly induced ROS production in human umbilical vein endothelial cells (HUVECs), and also mediated LPS-induced ROS production by HUVECs. Reactive Oxygen Species 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20732995-6 2010 MIMLh5 efficiently reduced the induction of interleukin-6 (IL-6), IL-8, and tumor necrosis factor alpha (TNF-alpha), in a dose-dependent manner. mimlh5 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 20632048-6 2010 In addition, nickel was shown to activate NF-kappaB and to induce the production of IL-8 in these cells. Nickel 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 20889551-8 2010 Taken together, the results indicate that ribotoxin-induced CHOP protein is positively associated with production of proinflammatory cytokine IL-8, but it downregulates PPARgamma action, subsequently allowing the cytosolic translocation of HuR protein and stabilization of IL-8 mRNA in gut epithelial cells. ribotoxin 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 20386089-9 2010 The VDR agonist elocalcitol partially reverts COX-2 and IL-8 mRNA upregulation induced by a pro-inflammatory cytokine mixture (IL-17, interferon-gamma, tumor necrosis factor-alpha) and inhibits cell migration in urethral cells. BXL628 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 20822922-13 2010 Reverse transcription polymerase chain reaction for IL-8 messenger RNA was significantly higher in controls during the reperfusion period than in the NAC group (p = 0.001). Acetylcysteine 150-153 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 21256400-7 2010 The test rinse significantly inhibited enamel surface softening versus the three rinses containing <=112 ppm fluoride (as NaF) at 30 min (p<0.05), but was not statistically significantly different from the 225 ppm fluoride rinse. Fluorides 112-120 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 20889551-8 2010 Taken together, the results indicate that ribotoxin-induced CHOP protein is positively associated with production of proinflammatory cytokine IL-8, but it downregulates PPARgamma action, subsequently allowing the cytosolic translocation of HuR protein and stabilization of IL-8 mRNA in gut epithelial cells. ribotoxin 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 273-277 20816994-6 2010 KEY FINDINGS: The release of IL-8 and TNFalpha from THP-1 and HL-60 cells was significantly increased by treatment with terbinafine but not by fluconazole, suggesting that terbinafine can stimulate monocytes and increase the pro-inflammatory cytokine release. Terbinafine 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 20935477-8 2010 In vitro, ATROSAB inhibited typical TNF-mediated responses like apoptosis induction and activation of NFkappaB-dependent gene expression such as IL-6 and IL-8 production. atrosab 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20456615-9 2010 IL-6 and IL-8 production was increased by Pam(3) CSK(4) , flagellin, Poly I:C, and imiquimod, but not lipopolysaccharide (LPS). Poly I-C 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 20512787-4 2010 After 24 h, glutamine inhibited IL-8 production significantly (p<0.05) at 2, 5 and 10 mM (to 82, 73 and 72% of control), whereas leucine reduced IL-8 production significantly only at 10 mM (66%) and proline at 5 and 10 mM (71 and 52%). Glutamine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 20512787-4 2010 After 24 h, glutamine inhibited IL-8 production significantly (p<0.05) at 2, 5 and 10 mM (to 82, 73 and 72% of control), whereas leucine reduced IL-8 production significantly only at 10 mM (66%) and proline at 5 and 10 mM (71 and 52%). Leucine 132-139 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 20512787-8 2010 Our results indicate that glutamine, leucine and proline attenuate IL-8 production, probably through inhibition of NF-kappaB, and that they increase Akt phosphorylation in HepG2 cells. Glutamine 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 20512787-8 2010 Our results indicate that glutamine, leucine and proline attenuate IL-8 production, probably through inhibition of NF-kappaB, and that they increase Akt phosphorylation in HepG2 cells. Leucine 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 20512787-8 2010 Our results indicate that glutamine, leucine and proline attenuate IL-8 production, probably through inhibition of NF-kappaB, and that they increase Akt phosphorylation in HepG2 cells. Proline 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 20816994-6 2010 KEY FINDINGS: The release of IL-8 and TNFalpha from THP-1 and HL-60 cells was significantly increased by treatment with terbinafine but not by fluconazole, suggesting that terbinafine can stimulate monocytes and increase the pro-inflammatory cytokine release. Terbinafine 172-183 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 20816994-8 2010 Pretreatment with a MAP kinase/ERK kinase (MEK)1/2 inhibitor U0126 significantly suppressed the increase of IL-8 and TNFalpha levels by terbinafine treatment in THP-1 cells, but p38 MAPK inhibitor SB203580 did not. U 0126 61-66 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 20816994-8 2010 Pretreatment with a MAP kinase/ERK kinase (MEK)1/2 inhibitor U0126 significantly suppressed the increase of IL-8 and TNFalpha levels by terbinafine treatment in THP-1 cells, but p38 MAPK inhibitor SB203580 did not. Terbinafine 136-147 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 20816994-9 2010 These results suggested that an ERK1/2 pathway plays an important role in the release of IL-8 and TNFalpha in THP-1 cells treated with terbinafine. Terbinafine 135-146 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 20841991-2 2010 Lopinavir, the most potent inducer of interleukin (IL)-8 expression, also inhibited dsRNA-induced monocyte chemotactic protein 1 expression. Lopinavir 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 38-56 21042538-5 2010 Stimulation with each agonist (Pam(3)CSK(4) for TLR2, LPS for TLR4, Tri-DAP for NOD1, and MDP for NOD2) led to IL-8 production in hUCB-MSC, suggesting the expressed receptors are functional in hUCB-MSC. L-Ala-gamma-D-Glu-meso-diaminopimelic acid 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 20841991-3 2010 Further analyses demonstrated that nuclear factor-kappaB is required for lopinavir"s induction of IL-8. Lopinavir 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 21042414-1 2010 5-Androstene-3beta,7beta,17beta-triol (beta-AET), an active metabolite of dehydroepiandrosterone (DHEA), reversed glucocorticoid (GC)-induced suppression of IL-6, IL-8 and osteoprotegerin production by human osteoblast-like MG-63 cells and promoted osteoblast differentiation of human mesenchymal stem cells (MSCs). 5-androstene-3beta 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 20958969-12 2010 Exposure of C3A cells to PA up-regulated IL-8 and TLR-4 expression. Palmitic Acid 25-27 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 21042414-1 2010 5-Androstene-3beta,7beta,17beta-triol (beta-AET), an active metabolite of dehydroepiandrosterone (DHEA), reversed glucocorticoid (GC)-induced suppression of IL-6, IL-8 and osteoprotegerin production by human osteoblast-like MG-63 cells and promoted osteoblast differentiation of human mesenchymal stem cells (MSCs). 7beta 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 21042414-1 2010 5-Androstene-3beta,7beta,17beta-triol (beta-AET), an active metabolite of dehydroepiandrosterone (DHEA), reversed glucocorticoid (GC)-induced suppression of IL-6, IL-8 and osteoprotegerin production by human osteoblast-like MG-63 cells and promoted osteoblast differentiation of human mesenchymal stem cells (MSCs). 17beta-triol 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 21042414-1 2010 5-Androstene-3beta,7beta,17beta-triol (beta-AET), an active metabolite of dehydroepiandrosterone (DHEA), reversed glucocorticoid (GC)-induced suppression of IL-6, IL-8 and osteoprotegerin production by human osteoblast-like MG-63 cells and promoted osteoblast differentiation of human mesenchymal stem cells (MSCs). 5-androstene-3,7,17-triol 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 21042414-1 2010 5-Androstene-3beta,7beta,17beta-triol (beta-AET), an active metabolite of dehydroepiandrosterone (DHEA), reversed glucocorticoid (GC)-induced suppression of IL-6, IL-8 and osteoprotegerin production by human osteoblast-like MG-63 cells and promoted osteoblast differentiation of human mesenchymal stem cells (MSCs). Dehydroepiandrosterone 74-96 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 21042414-1 2010 5-Androstene-3beta,7beta,17beta-triol (beta-AET), an active metabolite of dehydroepiandrosterone (DHEA), reversed glucocorticoid (GC)-induced suppression of IL-6, IL-8 and osteoprotegerin production by human osteoblast-like MG-63 cells and promoted osteoblast differentiation of human mesenchymal stem cells (MSCs). Dehydroepiandrosterone 98-102 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 20731619-10 2010 Inactivation of ERK signaling pathways by PD98059 effectively blocked IL-6, -8, and -10 induction by WTC2.5; the p38 kinase inhibitor SB203580 significantly decreased induction of IL-8 and -10. SB 203580 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 180-192 20139132-6 2010 The results of the potentiodynamic curve showed that most brands of metal brackets were easily corroded in the NaF and pH 4 environments, while the NiTi and stainless steel wires were easily corroded in the pH 4 artificial saliva. Metals 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 20678598-0 2010 Ginsenoside Rb1 and paeoniflorin inhibit transient receptor potential vanilloid-1-activated IL-8 and PGE2 production in a human keratinocyte cell line HaCaT. peoniflorin 20-32 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 21122279-0 2010 Montelukast reduces eosinophilic inflammation by inhibiting both epithelial cell cytokine secretion (GM-CSF, IL-6, IL-8) and eosinophil survival. montelukast 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 20939898-6 2010 ISO-1 ((S, R)-3-(4-hydroxyphenyl)-4,5-dihydro-5-isoxazole acetic acid methyl ester), a small-molecule inhibitor of MIF, significantly decreased IL-6, IL-8, and TNF-alpha production in a time- and dose-dependent manner in human peripheral blood cells infected with V. vulnificus. (s, r)-3-(4-hydroxyphenyl)-4,5-dihydro-5-isoxazole acetic acid methyl ester 7-82 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 20224070-4 2010 METHODS: Corticosteroid sensitivity was determined as the 50% inhibitory concentration of dexamethasone on tumor necrosis factor-alpha-induced interleukin-8 release in peripheral blood mononuclear cells from patients with COPD (n = 17) and compared with that of nonsmoking (n = 8) and smoking (n = 7) control subjects. Dexamethasone 90-103 C-X-C motif chemokine ligand 8 Homo sapiens 143-156 20339855-8 2010 RESULTS: 7beta-OH and 7KC triggered a caspase-independent cell death process associated with the presence of multilamellar cytoplasmic structures evocating phospholipidosis, increased ROS production, and IL-8 secretion. cholest-5-en-3 beta,7 alpha-diol 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 20339855-12 2010 25-OH induced IL-8 secretion through the MEK/ERK1/2 signaling pathway, and Rsv showed cytoprotective activities and inhibited VEGF secretion. 25-hydroxycholesterol 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 20678598-3 2010 It has been shown that GRb1 and PF inhibited the productions of IL-8 and PGE2 induced by capsaicin (CAP) in HaCaT cells and HEK 293T-TRPV1 cells (which were transgenic and overexpressed TRPV1) but had no effect on HEK 293T mock cells (p<0.05). Capsaicin 89-98 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 21535503-5 2010 Our data demonstrated that kaempferol significantly inhibited the lipopolysaccharide (LPS)-induced production of monocyte-derived chemokine (MDC), interferon gamma-induced protein 10 (IP-10), and interleukin-8 (IL-8) in THP-1 cells. kaempferol 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 196-209 21535503-5 2010 Our data demonstrated that kaempferol significantly inhibited the lipopolysaccharide (LPS)-induced production of monocyte-derived chemokine (MDC), interferon gamma-induced protein 10 (IP-10), and interleukin-8 (IL-8) in THP-1 cells. kaempferol 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 20397192-7 2010 The most important mechanism by which MG and GL induced IL-8 secretion was the generation of superoxide anions which was confirmed by the inhibition of the cytosolic NADPH oxidase with diphenyl iodonium (DPI) or by application of superoxide dismutase (SOD). Superoxides 93-110 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 19864123-2 2010 Mechanisms of CGN-induced nuclear factor kappaB and interleukin-8 (IL-8) stimulation include an immune-mediated pathway involving toll-like receptor 4 (TLR4) and B-cell lymphoma/leukemia 10 (BCL10) and a reactive oxygen species (ROS)-mediated pathway. Reactive Oxygen Species 204-227 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 19864123-2 2010 Mechanisms of CGN-induced nuclear factor kappaB and interleukin-8 (IL-8) stimulation include an immune-mediated pathway involving toll-like receptor 4 (TLR4) and B-cell lymphoma/leukemia 10 (BCL10) and a reactive oxygen species (ROS)-mediated pathway. Reactive Oxygen Species 229-232 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 21103419-2 2010 Upon exposure to HCl, inflammation of the esophagus begins with activation of the transient receptor potential channel vanilloid subfamily member-1 (TRPV1) in the mucosa, and production of IL-8, substance P (SP), calcitonin gene related peptide (CGRP) and platelet activating factor (PAF). Hydrochloric Acid 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 20828314-4 2010 To provide insight into the biological effects of tetrahydropalmatine, we examined its influence on lipopolysaccharide (LPS)-induced interleukin (IL)-8 production in the human monocytic cell line THP-1. tetrahydropalmatine 50-69 C-X-C motif chemokine ligand 8 Homo sapiens 133-151 20828314-6 2010 Tetrahydropalmatine inhibited LPS-induced IL-8 production in a dose-dependent manner. tetrahydropalmatine 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 20828314-7 2010 Furthermore, tetrahydropalmatine inhibited extracellular signal-regulated kinase and p38 MAPK phosphorylation, which suggests that tetrahydropalmatine inhibits IL-8 secretion by blocking MAPK phosphorylation. tetrahydropalmatine 13-32 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 20828314-7 2010 Furthermore, tetrahydropalmatine inhibited extracellular signal-regulated kinase and p38 MAPK phosphorylation, which suggests that tetrahydropalmatine inhibits IL-8 secretion by blocking MAPK phosphorylation. tetrahydropalmatine 131-150 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 20397192-0 2010 Carbonyl compounds methylglyoxal and glyoxal affect interleukin-8 secretion in intestinal cells by superoxide anion generation and activation of MAPK p38. carbonyl compounds 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 20397192-0 2010 Carbonyl compounds methylglyoxal and glyoxal affect interleukin-8 secretion in intestinal cells by superoxide anion generation and activation of MAPK p38. Glyoxal 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 20397192-7 2010 The most important mechanism by which MG and GL induced IL-8 secretion was the generation of superoxide anions which was confirmed by the inhibition of the cytosolic NADPH oxidase with diphenyl iodonium (DPI) or by application of superoxide dismutase (SOD). diphenyliodonium 204-207 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 20397192-0 2010 Carbonyl compounds methylglyoxal and glyoxal affect interleukin-8 secretion in intestinal cells by superoxide anion generation and activation of MAPK p38. Superoxides 99-115 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 20397192-3 2010 Hence, we investigated the impact of mitogen-activated protein kinases (MAPK) and nuclear factor kappa B (NF-kappaB) on IL-8 production by human intestinal cells (Caco-2 and HT-29) after stimulation by MG and GL. Pyruvaldehyde 202-204 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 20397192-7 2010 The most important mechanism by which MG and GL induced IL-8 secretion was the generation of superoxide anions which was confirmed by the inhibition of the cytosolic NADPH oxidase with diphenyl iodonium (DPI) or by application of superoxide dismutase (SOD). Pyruvaldehyde 38-40 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 20397192-7 2010 The most important mechanism by which MG and GL induced IL-8 secretion was the generation of superoxide anions which was confirmed by the inhibition of the cytosolic NADPH oxidase with diphenyl iodonium (DPI) or by application of superoxide dismutase (SOD). Glyoxal 45-47 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 20397192-8 2010 Our data suggest that multiple pathways were simultaneously activated; however, superoxide dependent MAPK p38 activation seems to be the most dominant pathway for IL-8 secretion in intestinal cells. Superoxides 80-90 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 20538801-4 2010 WPBs could also contain tPA, and in IL-1beta-treated cells, IL-8, IL-6, MCP-1, and GRO-alpha, and were the primary source for histamine or ionomycin-stimulated secretion of these molecules. Ionomycin 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 20633634-3 2010 IL-8 secretion and PGE-2 synthesizing capacity were dose-dependently upregulated in differentiated Caco-2 cells exposed to DON during 24h, reaching an increase of ~25 and 1.7-fold respectively, whereas transcript level of IL-8 and COX-2 were increased by ~40 and 17-fold. deoxynivalenol 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 20633634-3 2010 IL-8 secretion and PGE-2 synthesizing capacity were dose-dependently upregulated in differentiated Caco-2 cells exposed to DON during 24h, reaching an increase of ~25 and 1.7-fold respectively, whereas transcript level of IL-8 and COX-2 were increased by ~40 and 17-fold. deoxynivalenol 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 20633634-6 2010 IL-8 secretion and PGE-2 synthesizing capacity increased respectively by ~15 and 2-fold after chronic 21 day incubation with DON (50 ng/ml). deoxynivalenol 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 20941359-8 2010 Two of these genes, CEACAM1 and MMP8, possibly inhibited by methylprednisolone through IL8, were both found to be over-expressed in non-responsive patients. Methylprednisolone 60-78 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 20875145-7 2010 Pretreatment with GF109203X, a protein kinase C (PKC) inhibitor, completely normalized the effect of methacholine on CSE-induced IL-8 secretion, whereas PMA, a PKC activator, mimicked the effects of methacholine, inducing IL-8 secretion and augmenting the effects of CSE. bisindolylmaleimide I 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 20875145-7 2010 Pretreatment with GF109203X, a protein kinase C (PKC) inhibitor, completely normalized the effect of methacholine on CSE-induced IL-8 secretion, whereas PMA, a PKC activator, mimicked the effects of methacholine, inducing IL-8 secretion and augmenting the effects of CSE. bisindolylmaleimide I 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 20875145-7 2010 Pretreatment with GF109203X, a protein kinase C (PKC) inhibitor, completely normalized the effect of methacholine on CSE-induced IL-8 secretion, whereas PMA, a PKC activator, mimicked the effects of methacholine, inducing IL-8 secretion and augmenting the effects of CSE. Methacholine Chloride 101-113 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 20875145-10 2010 CONCLUSIONS: We conclude that muscarinic receptors facilitate CSE-induced IL-8 secretion by hASMc via PKC dependent activation of IkappaBalpha and ERK1/2. hasmc 92-97 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 20713890-4 2010 Activation of TLR9 by viral DNA requires endosomal maturation because pretreatment of monocytes with chloroquine strongly reduced IL-8 secretion. Chloroquine 101-112 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 20722440-0 2010 Oenothera paradoxa defatted seeds extract and its bioactive component penta-O-galloyl-beta-D-glucose decreased production of reactive oxygen species and inhibited release of leukotriene B4, interleukin-8, elastase, and myeloperoxidase in human neutrophils. penta-o-galloyl-beta-d-glucose 70-100 C-X-C motif chemokine ligand 8 Homo sapiens 190-213 20722440-8 2010 The extract and especially penta-O-galloyl-beta-D-glucose significantly inhibit elastase, myeloperoxidase IL-8, and LTB4 release with an IC50 for penta-O-galloyl-beta-D-glucose of 17+-1, 15+-1, 6.5+-2.5, and around 20 muM, respectively. penta-o-galloyl-beta-d-glucose 27-57 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 20800791-8 2010 CraA-induced IL-8 secretion can be blocked by serine protease inhibitors, phenylmethane sulfonyl fluoride, and aprotinin but not by other protease inhibitors. craa 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 20595617-8 2010 The H(2)O(2)-mediated potentiation of IL-8 production required the activity of p38, tyrosine kinases, phospholipase Cgamma, and intracellular calcium, but not protein kinase C or protein kinase D. H(2)O(2) prolonged and augmented NF-kappaB activation by flagellin. Calcium 142-149 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 20696864-4 2010 Surprisingly, however, whereas mRNA expression and cellular release of TNF-alpha, the beta form of pro-IL-1 (IL-1beta), and IL-6 were inhibited by the leptomycin B-induced nuclear IkappaBalpha, IL-8 mRNA expression and cellular release were not significantly affected. leptomycin B 151-163 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 20800791-11 2010 Furthermore, ERK1/2 (U0126) and JNK (SP600125) inhibitors inhibited CraA-induced IL-8 secretion by 100% and 45%, respectively. U 0126 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 20800791-11 2010 Furthermore, ERK1/2 (U0126) and JNK (SP600125) inhibitors inhibited CraA-induced IL-8 secretion by 100% and 45%, respectively. pyrazolanthrone 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 20800791-8 2010 CraA-induced IL-8 secretion can be blocked by serine protease inhibitors, phenylmethane sulfonyl fluoride, and aprotinin but not by other protease inhibitors. 4-toluenesulfonyl fluoride 74-105 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 20431935-7 2010 Conversely, the promoting effect of the variant allele of the IL-8 polymorphism was more remarkable in subjects with low plasma levels of Lutein/zeaxanthin, beta-cryptoxanthin, and beta-carotene (<median) [e.g., OR (95% CI): 2.44 (1.08, 5.75) (AT/TT vs. AA) for beta-carotene]. Beta-Cryptoxanthin 157-175 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 20595649-4 2010 In vitro, Pb induced an increase in interleukin 8 production and secretion by vascular endothelial cells. Lead 10-12 C-X-C motif chemokine ligand 8 Homo sapiens 36-49 20431935-7 2010 Conversely, the promoting effect of the variant allele of the IL-8 polymorphism was more remarkable in subjects with low plasma levels of Lutein/zeaxanthin, beta-cryptoxanthin, and beta-carotene (<median) [e.g., OR (95% CI): 2.44 (1.08, 5.75) (AT/TT vs. AA) for beta-carotene]. beta Carotene 181-194 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 20431935-7 2010 Conversely, the promoting effect of the variant allele of the IL-8 polymorphism was more remarkable in subjects with low plasma levels of Lutein/zeaxanthin, beta-cryptoxanthin, and beta-carotene (<median) [e.g., OR (95% CI): 2.44 (1.08, 5.75) (AT/TT vs. AA) for beta-carotene]. beta Carotene 265-278 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 20678032-6 2010 RESULTS: Our magnetic immunoassay could detect four attomoles of model proteins (hIL-8, hIgE) in phosphate buffer without BF separation. Phosphates 97-106 C-X-C motif chemokine ligand 8 Homo sapiens 81-86 20920411-8 2010 RESULTS: Polyethylene occlusion alone with abrupt removal induced IL-8 and IL-1alpha levels similar to or exceeding that of SLS. Polyethylene 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 20920411-10 2010 CONCLUSION: Removal of occlusion with polyethylene film up-regulates the inflammatory cytokines IL-8, IL-1alpha, and IL-1RA in patients with AD. Polyethylene 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 20095806-0 2010 Long-term effect of high doses glucocorticosteroids on mRNA expression for IL-6 and IL-8 in relapsed multiple sclerosis patients. glucocorticosteroids 31-51 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 20450371-5 2010 RESULTS: Subjects who presented generalized AgP have a higher frequency of hypomethylation of the IL8 gene promoter in oral epithelium cells than that of controls (86.5% in the generalized AgP group versus 62% in the control group; P = 0.016; chi(2) test). agp 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 20816188-8 2010 Atopic and atopic asthmatic subjects had increased sputum neutrophil numbers and IL-8 levels after ozone exposure; values did not significantly change in healthy volunteers. Ozone 99-104 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 20525739-5 2010 In comparison with chemokine production rate, the CXCL8 and CXCL10 production rates were significantly higher in pSS than in non-SS sicca controls (P < 0.01 by the Mann-Whitney test). pss 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 20553837-4 2010 Further, AexU prevented phosphorylation of c-Jun, JNK and IkappaBalpha and inhibited IL-6 and IL-8 secretion from HeLa cells. aexu 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 20812134-5 2010 In addition, ROC induces a significant decrease in ICAM expression and IL-8 release. Saquinavir 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 21038022-13 2010 Erythromycin given in group II decreased the levels of IL-8 and ICAM-1. Erythromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 20840147-8 2010 However, IL-8 induction was inhibited by small-interfering RNA against TLR5 or by treating flagella with disialoganglioside-GD1a, a TLR5 blocker. sialogangliosides 105-123 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 20347984-2 2010 The aim of this study was to evaluate the effect in cell culture of the third generation DHP-CA Manidipine on the release of interleukin-6 (IL-6) and interleukin-8 (IL-8) from human endothelial cells and human macrophages, in response to different pro-inflammatory signals. dhp-ca manidipine 89-106 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 20347984-2 2010 The aim of this study was to evaluate the effect in cell culture of the third generation DHP-CA Manidipine on the release of interleukin-6 (IL-6) and interleukin-8 (IL-8) from human endothelial cells and human macrophages, in response to different pro-inflammatory signals. dhp-ca manidipine 89-106 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 20347984-5 2010 In these cells TNF-alpha increased by about 4 times the secretion of IL-8 and Manidipine 5 microM reduced the amount of IL-8 in the culture media by about 40%. manidipine 78-88 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 21221176-10 2010 The in-vitro experiment I resulted for NaF in 251.7+-22.4 microg/g fluoride and for amine fluoride in 171.7+-14.4 microg/g. Fluorides 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 21221176-11 2010 CONCLUSIONS: Fluoride bioavailability of saliva after exposure to NaF was higher compared to amine fluoride. Fluorides 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 66-69 20649610-7 2010 Moreover, iloprost dose dependently inhibited the secretion of TNF-alpha, IL-6, IL-8 and IL-12p70 in mDCs, while it enhanced IL-10 production. Iloprost 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 23662086-0 2010 Remineralization of eroded enamel by a NaF rinse containing a novel calcium phosphate agent in an in situ model: a pilot study. calcium phosphate 68-85 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 20707554-1 2010 Molecular dynamics simulations are carried out to study the interfacial profiles of alkali metal fluoride solutions (NaF, KF, RbF, and CsF) at 1 atm and 300 K. For these solutions, we find that the occupancy of the cations in the interfacial region is comparable to or greater than that of the F(-) anion. metal fluoride 91-105 C-X-C motif chemokine ligand 8 Homo sapiens 117-120 20711426-12 2010 CONCLUSIONS/SIGNIFICANCE: The results clearly demonstrate that damage to the bronchial epithelia by poly-L-arginine stimulates polarized IL-6 and IL-8 secretion. polyarginine 100-115 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 20711431-5 2010 We found that purified HCP and a recombinant HcpA protein induced significant release of IL-8 and TNF-alpha, from cultured polarized intestinal cells (T84 and HT-29 cells) and non-intestinal HeLa cells. hcp 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 20711431-6 2010 Levels of proinflammatory IL-8 and TNF-alpha, but not IL-2, IL6, or IL-10 cytokines, were increased in the presence of HCP and recombinant HcpA after 6 h of incubation with >or=50 ng/ml of protein, suggesting that stimulation of IL-8 and TNF-alpha are dose and time-dependent. hcp 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20711431-6 2010 Levels of proinflammatory IL-8 and TNF-alpha, but not IL-2, IL6, or IL-10 cytokines, were increased in the presence of HCP and recombinant HcpA after 6 h of incubation with >or=50 ng/ml of protein, suggesting that stimulation of IL-8 and TNF-alpha are dose and time-dependent. hcp 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 20505677-4 2010 We found that losartan significantly attenuated the LPS-induced expression of proinflammatory genes TNF-alpha, IL-8 and COX-2. Losartan 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 19633914-4 2010 The effect of NaCl, Na2SO4, NaF, NaBr, Na3PO4, and other interfering salts on the sorption of metal ions (50 microg L(-1)) was reported. Metals 94-99 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 20815772-2 2010 When HNSCC cells were cultured in the presence of ROS, the expression of BRAK was significantly decreased whereas that of IL-8 was increased. Reactive Oxygen Species 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 20815772-4 2010 The effects of ROS on both BRAK and IL-8 expression were attenuated by pre-treatment with N-acetyl-L-cysteine (NAC), epidermal growth factor receptor (EGFR), and mitogen-activated protein kinase (MAPK) inhibitors. Reactive Oxygen Species 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 20815772-4 2010 The effects of ROS on both BRAK and IL-8 expression were attenuated by pre-treatment with N-acetyl-L-cysteine (NAC), epidermal growth factor receptor (EGFR), and mitogen-activated protein kinase (MAPK) inhibitors. Acetylcysteine 90-109 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 20505677-7 2010 Peroxisome proliferator-activated receptor-gamma (PPARgamma) antagonists, GW9662 and T0070907, reversed the inhibitory effects of losartan on LPS-induced TNF-alpha and IL-8 expression in THP-1 macrophages. 2-chloro-5-nitrobenzanilide 74-80 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 20505677-7 2010 Peroxisome proliferator-activated receptor-gamma (PPARgamma) antagonists, GW9662 and T0070907, reversed the inhibitory effects of losartan on LPS-induced TNF-alpha and IL-8 expression in THP-1 macrophages. Losartan 130-138 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 20412422-7 2010 Scavenger receptor inhibitors, fucoidan and dextran sulfate, inhibited the OxLDL-induced IL-8 and PGE(2) production in the presence of IL-1 beta. fucoidan 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 20438865-5 2010 At the same time, muropeptide-stimulated DCs abundantly produced inflammatory chemokines IL-8, MIP-1 alpha and MIP-1 beta, as well as displayed signs of phenotypic and functional maturation. muropeptide 18-29 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 20515921-3 2010 In the present study, we investigated ATP release from uroepithelial cells infected with bacteria and the effect of ATP on the host cell proinflammatory interleukin 8 (IL-8) response. Adenosine Triphosphate 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 153-166 20515921-3 2010 In the present study, we investigated ATP release from uroepithelial cells infected with bacteria and the effect of ATP on the host cell proinflammatory interleukin 8 (IL-8) response. Adenosine Triphosphate 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 20515921-7 2010 ATP-gamma-S (10 and 100 microM) stimulated release of IL-8 from UROtsa and A498 cells after 6 and 24 h. Experiments with different purinoceptor agonists suggested that P2Y receptors, and not P2X receptors, were responsible for the ATP-gamma-S-induced IL-8 release. adenosine 5'-O-(3-thiotriphosphate) 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 20515921-7 2010 ATP-gamma-S (10 and 100 microM) stimulated release of IL-8 from UROtsa and A498 cells after 6 and 24 h. Experiments with different purinoceptor agonists suggested that P2Y receptors, and not P2X receptors, were responsible for the ATP-gamma-S-induced IL-8 release. adenosine 5'-O-(3-thiotriphosphate) 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 20515921-10 2010 The present study suggests that enhanced ATP release and P2Y receptor activation during urinary tract infection may represent a novel, non-TLR4-mediated mechanism for production of proinflammatory IL-8 in human urinary tract epithelial cells. Adenosine Triphosphate 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 20412422-7 2010 Scavenger receptor inhibitors, fucoidan and dextran sulfate, inhibited the OxLDL-induced IL-8 and PGE(2) production in the presence of IL-1 beta. Dextran Sulfate 44-59 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 20412422-8 2010 The p(38) MAPK inhibitors SB203580 and SB202190 and the ERK inhibitor PD98059 inhibited the OxLDL-induced IL-8 production. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 20412422-9 2010 Among oxidized lipids and chemically modified LDL, 7-ketocholesterol enhanced IL-8 production. 7-ketocholesterol 51-68 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 20307681-4 2010 Formoterol enhanced and budesonide inhibited IL-6, CXCL8 and CXCL1 release from LPS-stimulated neutrophils. Budesonide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 51-56 20112302-7 2010 IL-8 messenger RNA expression and IL-8 production in the epithelial cells increased following the hemin treatment, but the production was inhibited by ZnPP and catalase. zinc protoporphyrin 151-155 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 20434478-8 2010 Treatment with ZnO (5mug/cm(2) corresponding to 11.5mug/ml) for 24h induced on LoVo cells a significant decrease of cell viability, H2O2/OH increase, O2(-) and GSH decrease, depolarization of inner mitochondrial membranes, apoptosis and IL-8 release. Zinc Oxide 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 237-241 20578705-8 2010 Incubation of ARPE-19 cells with 33 mM glucose for 9 days significantly induced the accumulation of VEGF, IL-6, IL-8, TGF-beta, and COX-2, activation of PKCbeta, and reduction of Cx43 and GJIC. Glucose 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 20578705-9 2010 Incubation of ARPE-19 cells with 33 mM glucose in the presence of 0-10 microM trans-resveratrol dose-dependently inhibited VEGF, TGF-beta1, COX-2, IL-6, and IL-8 accumulation, PKCbeta activation, and Cx43 degradation and enhanced GJIC. Glucose 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 20578705-9 2010 Incubation of ARPE-19 cells with 33 mM glucose in the presence of 0-10 microM trans-resveratrol dose-dependently inhibited VEGF, TGF-beta1, COX-2, IL-6, and IL-8 accumulation, PKCbeta activation, and Cx43 degradation and enhanced GJIC. Resveratrol 78-95 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 20510674-0 2010 Thromboxane A(2) increases endothelial permeability through upregulation of interleukin-8. thromboxane a 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 20626862-0 2010 Pneumocystis cell wall beta-glucan stimulates calcium-dependent signaling of IL-8 secretion by human airway epithelial cells. beta-Glucans 23-34 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 20626862-0 2010 Pneumocystis cell wall beta-glucan stimulates calcium-dependent signaling of IL-8 secretion by human airway epithelial cells. Calcium 46-53 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 20626862-3 2010 Several previous studies indicate that airway epithelial cells release the neutrophil chemoattractant proteins, MIP-2 (rodents) and IL-8 (humans), in response to Pneumocystis and purified Pneumocystis cell wall beta-glucans (PCBG) through the NF-kappaB-dependent pathway. beta-Glucans 211-223 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 20626862-3 2010 Several previous studies indicate that airway epithelial cells release the neutrophil chemoattractant proteins, MIP-2 (rodents) and IL-8 (humans), in response to Pneumocystis and purified Pneumocystis cell wall beta-glucans (PCBG) through the NF-kappaB-dependent pathway. S-(1,2,3,4,4-Pentachloro-1,3-butadienyl)glutathione 225-229 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 20626862-4 2010 However, little is known about the molecular mechanisms that are involved in the activation of airway epithelium cells by PCBG resulting in the secretion of IL-8. S-(1,2,3,4,4-Pentachloro-1,3-butadienyl)glutathione 122-126 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 20626862-6 2010 RESULTS: Our data provide evidence that PCBG induces phosphorylation of the MAPKs, ERK, and p38, the activation of NF-kappaB and the subsequently secretion of IL-8 in a calcium-dependent manner. S-(1,2,3,4,4-Pentachloro-1,3-butadienyl)glutathione 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 20626862-6 2010 RESULTS: Our data provide evidence that PCBG induces phosphorylation of the MAPKs, ERK, and p38, the activation of NF-kappaB and the subsequently secretion of IL-8 in a calcium-dependent manner. Calcium 169-176 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 20626862-8 2010 Preincubation of the cells with D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP) a potent inhibitor of the glycosphingolipids synthesis, prior to PCBG stimulation, significantly decreased IL-8 production. RV 538 32-88 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 20626862-8 2010 Preincubation of the cells with D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP) a potent inhibitor of the glycosphingolipids synthesis, prior to PCBG stimulation, significantly decreased IL-8 production. RV 538 90-94 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 20626862-9 2010 CONCLUSION: These data indicate that PCBG activates calcium dependent MAPK signaling resulting in the release of IL-8 in a process that requires glycosphingolipid for optimal signaling. S-(1,2,3,4,4-Pentachloro-1,3-butadienyl)glutathione 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 20626862-9 2010 CONCLUSION: These data indicate that PCBG activates calcium dependent MAPK signaling resulting in the release of IL-8 in a process that requires glycosphingolipid for optimal signaling. Calcium 52-59 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 20626862-9 2010 CONCLUSION: These data indicate that PCBG activates calcium dependent MAPK signaling resulting in the release of IL-8 in a process that requires glycosphingolipid for optimal signaling. Glycosphingolipids 145-162 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 20504277-5 2010 RESULTS: Treatment of cultured endothelial cells with sodium fluoride (NaF) results in a rapid and potent stimulation of podosome formation. Sodium Fluoride 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 20508179-12 2010 The inhibitory effect of Dll4 on interleukin-8 was abolished by DAPT, a Notch inhibitor, or by coculturing activated human monocytes with Ad-sDll4-infected endothelial cells. dapt 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 20663736-4 2010 With the advent of hybrid positron emission tomography (PET)/CT scanners there has been an increasing interest in using various PET tracers to evaluate skeletal disease including [(18)F]fluoride (NaF) as a bone-specific tracer and [(18)F]fluorodeoxyglucose and [(18)F]choline as tumour-specific tracers. Fluorides 186-194 C-X-C motif chemokine ligand 8 Homo sapiens 196-199 20663736-4 2010 With the advent of hybrid positron emission tomography (PET)/CT scanners there has been an increasing interest in using various PET tracers to evaluate skeletal disease including [(18)F]fluoride (NaF) as a bone-specific tracer and [(18)F]fluorodeoxyglucose and [(18)F]choline as tumour-specific tracers. Fluorodeoxyglucose F18 238-256 C-X-C motif chemokine ligand 8 Homo sapiens 196-199 20663736-4 2010 With the advent of hybrid positron emission tomography (PET)/CT scanners there has been an increasing interest in using various PET tracers to evaluate skeletal disease including [(18)F]fluoride (NaF) as a bone-specific tracer and [(18)F]fluorodeoxyglucose and [(18)F]choline as tumour-specific tracers. Choline 268-275 C-X-C motif chemokine ligand 8 Homo sapiens 196-199 20434448-0 2010 Rho-kinase mediates lysophosphatidic acid-induced IL-8 and MCP-1 production via p38 and JNK pathways in human endothelial cells. lysophosphatidic acid 20-41 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 20510674-7 2010 Overall, these results suggest that U46619 promotes vascular permeability through the production of IL-8 via NF-kappaB activation in endothelial cells. 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid 36-42 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 20194077-0 2010 Phosphorylation of p65 is required for zinc oxide nanoparticle-induced interleukin 8 expression in human bronchial epithelial cells. Zinc Oxide 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 20463039-10 2010 Furthermore, resveratrol down-regulated the expression and secretion of interleukin-6 and interleukin-8. Resveratrol 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 20194077-11 2010 Moreover, ZnO exposure also increased the binding of p65 to the IL-8 promoter and p65 phosphorylation at serines 276 and 536. Zinc Oxide 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 20378727-0 2010 17Beta-estradiol inhibits IL-8 in cystic fibrosis by up-regulating secretory leucoprotease inhibitor. Estradiol 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20185130-5 2010 We found that 5"-NIO inhibited TNF-alpha induced MCP-1 and IL-8 expression at the RNA and protein levels in HUVECs. 5'-nitroindirubinoxime 14-20 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 20185130-6 2010 Specifically, 5"-NIO significantly inhibited the TNF-alpha stimulated release of MCP-1 and IL-8, with levels that were only 19.8% and 30.9% of those of untreated control cells, respectively. 5'-nitroindirubinoxime 14-20 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 20206688-2 2010 The NF-kappaB-dependent gene expression of IL8, IL6, PTGS2/COX2, TNF and IL33 in directly irradiated human skin fibroblasts produced the cytokines and prostaglandin E2 (PGE2) with autocrine/paracrine functions, which further activated signaling pathways and induced NF-kappaB-dependent gene expression in bystander cells. Dinoprostone 151-167 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 20206688-2 2010 The NF-kappaB-dependent gene expression of IL8, IL6, PTGS2/COX2, TNF and IL33 in directly irradiated human skin fibroblasts produced the cytokines and prostaglandin E2 (PGE2) with autocrine/paracrine functions, which further activated signaling pathways and induced NF-kappaB-dependent gene expression in bystander cells. Dinoprostone 169-173 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 20206688-3 2010 As a result, bystander cells also started expression and production of interleukin-8, interleukin-6, COX-2-generated PGE2 and interleukin-33 (IL-33) followed by autocrine/paracrine stimulation of the NF-kappaB and MAPK pathways. Dinoprostone 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 20194077-12 2010 Overexpression of p65 constructs mutated at serines 276 or 536 significantly reduced ZnO-induced increase in IL-8 promoter reporter activity. Serine 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 20194077-12 2010 Overexpression of p65 constructs mutated at serines 276 or 536 significantly reduced ZnO-induced increase in IL-8 promoter reporter activity. Zinc Oxide 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 20194077-13 2010 CONCLUSION: p65 phosphorylation and IkappaBalpha phosphorylation and degradation are the primary mechanisms involved in ZnO nanoparticle-induced IL-8 expression in human bronchial epithelial cells. Zinc Oxide 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 20194077-1 2010 BACKGROUND: Exposure to zinc oxide (ZnO) in environmental and occupational settings causes acute pulmonary responses through the induction of proinflammatory mediators such as interleukin-8 (IL-8). Zinc Oxide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 20194077-1 2010 BACKGROUND: Exposure to zinc oxide (ZnO) in environmental and occupational settings causes acute pulmonary responses through the induction of proinflammatory mediators such as interleukin-8 (IL-8). Zinc Oxide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 20194077-1 2010 BACKGROUND: Exposure to zinc oxide (ZnO) in environmental and occupational settings causes acute pulmonary responses through the induction of proinflammatory mediators such as interleukin-8 (IL-8). Zinc Oxide 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 20194077-1 2010 BACKGROUND: Exposure to zinc oxide (ZnO) in environmental and occupational settings causes acute pulmonary responses through the induction of proinflammatory mediators such as interleukin-8 (IL-8). Zinc Oxide 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 20194077-2 2010 OBJECTIVE: We investigated the effect of ZnO nanoparticles on IL-8 expression and the underlying mechanisms in human bronchial epithelial cells. Zinc Oxide 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 20194077-4 2010 Transcriptional activity of IL-8 promoter and nuclear factor kappa B (NFkappaB) in ZnO-treated BEAS-2B cells was measured using transient gene transfection of the luciferase reporter construct with or without p65 constructs. Zinc Oxide 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 20194077-7 2010 RESULTS: ZnO exposure (2-8 microg/mL) increased IL-8 mRNA and protein expression. Zinc Oxide 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Dactinomycin 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Dactinomycin 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Zinc Oxide 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Zinc Oxide 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Zinc Oxide 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 19926732-6 2010 Formoterol and salmeterol inhibited LPS-stimulated release of TNF-alpha (mean effective concentration (EC(50)) 2.4+/-1.8 and 3.5+/-2.7 nM, respectively; n = 11-16), GM-CSF (EC(50) 24.6+/-2.1 and 52.4+/-40.8 nM, respectively, n = 11-12) but not CXCL8 from LPS-stimulated MDM. Formoterol Fumarate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 244-249 20194077-8 2010 Inhibition of transcription with actinomycin D blocked ZnO-induced IL-8 expression, which was consistent with the observation that ZnO exposure increased IL-8 promoter reporter activity. Zinc Oxide 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 19926732-6 2010 Formoterol and salmeterol inhibited LPS-stimulated release of TNF-alpha (mean effective concentration (EC(50)) 2.4+/-1.8 and 3.5+/-2.7 nM, respectively; n = 11-16), GM-CSF (EC(50) 24.6+/-2.1 and 52.4+/-40.8 nM, respectively, n = 11-12) but not CXCL8 from LPS-stimulated MDM. Salmeterol Xinafoate 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 244-249 20194077-9 2010 Further study demonstrated that the kappaB-binding site in the IL-8 promoter was required for ZnO-induced IL-8 transcriptional activation. Zinc Oxide 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 19926732-7 2010 Budesonide inhibited release of all three cytokines (EC(50) TNF-alpha: 1.2+/-0.4 nM; GM-CSF: 0.4+/-0.2 nM; CXCL8: 0.4+/-0.1 nM; n = 3-4). Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 107-112 20194077-9 2010 Further study demonstrated that the kappaB-binding site in the IL-8 promoter was required for ZnO-induced IL-8 transcriptional activation. Zinc Oxide 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 20479083-5 2010 The recombinant SSL5-Sepharose also bound to proMMP-9 secreted by interleukin 8 (IL-8)-stimulated neutrophils and HT1080 fibrosarcoma cells. Sepharose 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 20334899-3 2010 In HCT 116 and HCT-8 colorectal adenocarcinoma cells, the production of IL-8 immunoreactivity was up-regulated by IL-1beta, tumor necrosis factor (TNF)-alpha, the toll-like receptor (TLR) ligands double-stranded RNA and peptidoglycan and phorbol ester. Phorbol Esters 238-251 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 20557833-8 2010 The addition of linezolid significantly reduced mRNA levels of IL-1beta, IL-6, IL-8 and TNF-alpha; (p < 0.05) after 2 and 4 h. LPS stimulation also increased levels of IL-6, IL-8 and TNF-alpha between 100 and 1000-fold. Linezolid 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 20479083-5 2010 The recombinant SSL5-Sepharose also bound to proMMP-9 secreted by interleukin 8 (IL-8)-stimulated neutrophils and HT1080 fibrosarcoma cells. Sepharose 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 20416374-9 2010 This is approached through a few illustrative examples, including the interaction of HS and heparin-derived species with the chemokine IL-8, the growth factors FGF1 and FGF2, and the modulation of the activity of the enzyme heparanase by these species. Heparin 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 20819396-7 2010 Methotrexate given prior to the day 2 abrasions reduced neutrophil extravasation and IL8 levels compared with those on day 1. Methotrexate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 20819396-8 2010 rC5a partially abrogated the methotrexate-induced reduction in neutrophil extravasation and IL8 production. Methotrexate 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 21128470-1 2010 Highly ordered nanotube oxide layers were developed on low rigidity quaternary beta-type Ti-35Nb-5Ta-7Zr alloy by controlled anodic oxidation in electrolyte containing 1 M H3PO4 and 0.5 wt% NaF at room temperature. Oxides 24-29 C-X-C motif chemokine ligand 8 Homo sapiens 190-193 20557833-8 2010 The addition of linezolid significantly reduced mRNA levels of IL-1beta, IL-6, IL-8 and TNF-alpha; (p < 0.05) after 2 and 4 h. LPS stimulation also increased levels of IL-6, IL-8 and TNF-alpha between 100 and 1000-fold. Linezolid 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 20483454-3 2010 Interleukin (IL) 8 has been implicated as a regulator of EVT invasion. EVT 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 0-18 20618689-10 2010 The modest upregulation of IL-8 and IL-6 might be associated with the milder clinical manifestations of PCP in AIDS patients. pcp 104-107 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 20389259-1 2010 BACKGROUND: The aim of this prospective study is to evaluate the diagnostic and prognostic usefulness of F-18 sodium fluoride (NaF) positron emission tomography-computed tomography (PET-CT) relative to Tc-99m methylene diphosphonate (MDP) planar bone scintigraphy with no CT (BS) for hepatocellular carcinoma (HCC) patients with suspicious bone metastasis. Fluorine-18 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 20389259-1 2010 BACKGROUND: The aim of this prospective study is to evaluate the diagnostic and prognostic usefulness of F-18 sodium fluoride (NaF) positron emission tomography-computed tomography (PET-CT) relative to Tc-99m methylene diphosphonate (MDP) planar bone scintigraphy with no CT (BS) for hepatocellular carcinoma (HCC) patients with suspicious bone metastasis. Sodium Fluoride 110-125 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 20389259-1 2010 BACKGROUND: The aim of this prospective study is to evaluate the diagnostic and prognostic usefulness of F-18 sodium fluoride (NaF) positron emission tomography-computed tomography (PET-CT) relative to Tc-99m methylene diphosphonate (MDP) planar bone scintigraphy with no CT (BS) for hepatocellular carcinoma (HCC) patients with suspicious bone metastasis. Technetium Tc 99m Medronate 202-232 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 20389259-1 2010 BACKGROUND: The aim of this prospective study is to evaluate the diagnostic and prognostic usefulness of F-18 sodium fluoride (NaF) positron emission tomography-computed tomography (PET-CT) relative to Tc-99m methylene diphosphonate (MDP) planar bone scintigraphy with no CT (BS) for hepatocellular carcinoma (HCC) patients with suspicious bone metastasis. methylene diphosphonate 234-237 C-X-C motif chemokine ligand 8 Homo sapiens 127-130 20483454-4 2010 HYPOTHESIS: uNK cell stimulation of EVT invasion is associated with IL-8 levels. EVT 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20483454-12 2010 Exogenous IL-8 stimulated EVT invasion in a paracrine manner. EVT 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 20483454-16 2010 CONCLUSION: uNK cell stimulation of EVT invasion is partially mediated by IL-8. EVT 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 20591071-12 2010 Through ERK inhibitor (U0126) and NF-kB inhibitor (caffeine acid phenethyl ester) treatment, it was proven that ERK and NF-kB regulated chitinase-induced IL-8 expression. U 0126 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 19777241-6 2010 PGE(2) and IL-8 secretion was also induced by IL-1beta stimulation and significantly suppressed by EGCG. epigallocatechin gallate 99-103 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19777241-8 2010 EGCG may inhibit the expression of inflammatory mediators, such as COX-2, PGE(2), and IL-8, induced by IL-1beta in human synovial fibroblasts. epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 19777241-0 2010 Effects of (-)-epigallocatechin-3-gallate on cyclooxygenase 2, PGE(2), and IL-8 expression induced by IL-1beta in human synovial fibroblasts. epigallocatechin gallate 11-41 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 20591071-12 2010 Through ERK inhibitor (U0126) and NF-kB inhibitor (caffeine acid phenethyl ester) treatment, it was proven that ERK and NF-kB regulated chitinase-induced IL-8 expression. caffeine acid phenethyl ester 51-80 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20417223-5 2010 Data show that thimerosal and mercury derivatives induced DC activation, as monitored by CD86 and HLA-DR overexpression associated with the secretion of tumor necrosis factor alpha and interleukin 8, similarly to lipopolysaccharide and the sensitizers, 1-chloro-2,4-dinitrobenzene (DNCB) and nickel sulfate, which were used as positive controls. Thimerosal 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 185-198 20214469-5 2010 Additionally, 3D integrin engagement by RGD-modified alginate matrices increased IL-8 secretion independently of oxygen, whereas VEGF secretion was only moderately affected by cell-extracellular matrix interactions. Alginates 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 20417223-5 2010 Data show that thimerosal and mercury derivatives induced DC activation, as monitored by CD86 and HLA-DR overexpression associated with the secretion of tumor necrosis factor alpha and interleukin 8, similarly to lipopolysaccharide and the sensitizers, 1-chloro-2,4-dinitrobenzene (DNCB) and nickel sulfate, which were used as positive controls. Mercury 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 185-198 20457211-4 2010 Thimerosal and mercury derivatives induced in U937 an overexpression of CD86 and interleukin (IL)-8 secretion similarly to 1-chloro-2,4-dinitrobenzene (DNCB), a sensitizer used as a positive control for DC activation. Thimerosal 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 81-99 20457211-4 2010 Thimerosal and mercury derivatives induced in U937 an overexpression of CD86 and interleukin (IL)-8 secretion similarly to 1-chloro-2,4-dinitrobenzene (DNCB), a sensitizer used as a positive control for DC activation. Mercury 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 81-99 21055061-10 2010 Corresponding expression of NF-kappaB, IL-1beta, IL-8 and COX-2 decreased after the addition of Wedelolactone (relative values were 0.917 +- 0.188, 0.180 +- 0.008, 0, 0 respectively). wedelolactone 96-109 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 20731040-6 2010 FSEM showed that pure titanium and Ti-Ni-Cr alloy surface corrosion, pure titanium in the artificial saliva containing 0.2% NaF was most serious. Titanium 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 20531411-8 2010 Metronomic gemcitabine also significantly increased apoptosis in cancer-associated fibroblasts and induced greater reductions in the tumour levels of multiple pro-angiogenic factors, including EGF, IL-1alpha, IL-8, ICAM-1, and VCAM-1. gemcitabine 11-22 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 20206138-5 2010 In human HaCaT keratinocytes falcarinol increased the expression of the pro-allergic chemokines IL-8 and CCL2/MCP-1 in a CB(1) receptor-dependent manner. falcarinol 29-39 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 22911911-11 2010 CONCLUSION: The levels of serum pro-inflammatory cytokines IL-8 & TNF- alpha were significantly associated with subjects having respiratory symptoms & further supporting that they are inflammatory markers in respiratory symptoms. Adenosine Monophosphate 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 22911911-11 2010 CONCLUSION: The levels of serum pro-inflammatory cytokines IL-8 & TNF- alpha were significantly associated with subjects having respiratory symptoms & further supporting that they are inflammatory markers in respiratory symptoms. Adenosine Monophosphate 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 20206208-11 2010 Measurements of stimulated cytokine production demonstrated (i) that cumulative hypoxia stimulates especially the secretion of IL-1beta, IL-10 and IL-8, and (ii) that lack of glucose results in lower cytokine concentrations. Glucose 175-182 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 20354173-7 2010 The increase in IL-8 release occurred despite reduced IL-8 mRNA levels in the donor granulocytes after in vivo G-CSF/dexa treatment, indicating that the enhanced TLR-induced IL-8 production was largely determined by posttranscriptional regulation. Dexamethasone 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 20441516-3 2010 Albendazole treatment, compared with placebo, was associated with significantly decreased plasma interleukin (IL) 10 levels (P = .01)ot associated with significant changes in levels of IL-1beta, IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-12p70, IL-13, interferon gamma, tumor necrosis factor alpha, or thymic stromal lymphopoietin. Albendazole 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 20307528-5 2010 The RT-PCR, real-time PCR, and ELISA analyses demonstrated that LPS-induced mRNAs encoding IL-6 and IL-8 and the subsequent secretion of IL-6 and IL-8 were inhibited by glucosamine treatment. Glucosamine 169-180 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 20307528-5 2010 The RT-PCR, real-time PCR, and ELISA analyses demonstrated that LPS-induced mRNAs encoding IL-6 and IL-8 and the subsequent secretion of IL-6 and IL-8 were inhibited by glucosamine treatment. Glucosamine 169-180 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 20530802-2 2010 We found that neutrophils released cellular adenosine triphosphate (ATP) in response to exogenous stimuli such as formylated bacterial peptides and inflammatory mediators that activated Fcgamma, interleukin-8, C5a complement, and leukotriene B(4) receptors. Adenosine Triphosphate 44-66 C-X-C motif chemokine ligand 8 Homo sapiens 195-208 20530802-2 2010 We found that neutrophils released cellular adenosine triphosphate (ATP) in response to exogenous stimuli such as formylated bacterial peptides and inflammatory mediators that activated Fcgamma, interleukin-8, C5a complement, and leukotriene B(4) receptors. Adenosine Triphosphate 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 195-208 20451499-4 2010 Thrombin activated Akt, PKC and MAPK in HAoSMC, and thrombin-mediated expression of IL-6 and CXCL8 was significantly inhibited by LY294002, AKT IV, RO318220, and GF109203X as well as by diphenyleneiodium at the messenger RNA and the protein levels. bisindolylmaleimide I 162-171 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 20451499-4 2010 Thrombin activated Akt, PKC and MAPK in HAoSMC, and thrombin-mediated expression of IL-6 and CXCL8 was significantly inhibited by LY294002, AKT IV, RO318220, and GF109203X as well as by diphenyleneiodium at the messenger RNA and the protein levels. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 130-138 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 20451499-4 2010 Thrombin activated Akt, PKC and MAPK in HAoSMC, and thrombin-mediated expression of IL-6 and CXCL8 was significantly inhibited by LY294002, AKT IV, RO318220, and GF109203X as well as by diphenyleneiodium at the messenger RNA and the protein levels. Ro 31-8220 148-156 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 20371264-6 2010 Exposure of MWCNT (10-100mug/ml) to HEK cells resulted in concentration dependent cell membrane damage (as indicated by the increased levels of LDH), increased production of IL-8, increased TBARS and decreased intracellular glutathione levels. mwcnt 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 20451499-4 2010 Thrombin activated Akt, PKC and MAPK in HAoSMC, and thrombin-mediated expression of IL-6 and CXCL8 was significantly inhibited by LY294002, AKT IV, RO318220, and GF109203X as well as by diphenyleneiodium at the messenger RNA and the protein levels. diphenyleneiodium 186-203 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 20451499-5 2010 SB202129 and U0126 also significantly attenuated thrombin-mediated release of IL-6 and CXCL8 proteins from HAoSMC. U 0126 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 87-92 20092409-3 2010 We further observed that supplementation with H(2)S or an endogenous precursor of H(2)S (l-cysteine) in culture medium prevents IL-8 and MCP-1 secretion in high-glucose-treated human U937 monocytes. Hydrogen Sulfide 46-51 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 19930229-0 2010 Matrix metalloproteinases, IL-8 and glutathione in the prognosis of workers exposed to chlorine. Chlorine 87-95 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 20568377-6 2010 After treatment, forced expiratory volume in 1 second significantly increased and sputum eosinophil percentages and IL-5 and IL-8 concentrations significantly decreased in the prednisone group, whereas no changes were observed in the placebo group. Prednisone 176-186 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 20568377-7 2010 The positive effect of prednisone treatment was observed only in patients with baseline sputum eosinophilia, whereas in noneosinophilic patients with severe asthma prednisone induced only a significant decrease of sputum IL-8. Prednisone 164-174 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 20035908-0 2010 The effect of Na(2)CO(3), NaF and NH(4)OH on the stability and release behavior of sol-gel derived silica xerogels embedded with bioactive compounds. silica xerogels 99-114 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 19597128-4 2010 The effect of hydrogen peroxide (H(2)O(2)) on the release of IL-8 from BEAS-2B cells and primary human bronchial epithelial cells after stimulation with polyinosine-polycytidylic acid [poly(I:C)], a synthetic analog of viral dsRNA and a ligand for TLR3, and the signal transduction were examined. Hydrogen Peroxide 14-31 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 19597128-4 2010 The effect of hydrogen peroxide (H(2)O(2)) on the release of IL-8 from BEAS-2B cells and primary human bronchial epithelial cells after stimulation with polyinosine-polycytidylic acid [poly(I:C)], a synthetic analog of viral dsRNA and a ligand for TLR3, and the signal transduction were examined. polyinosine-polycytidylic acid 153-183 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 19597128-5 2010 One hundred to 150 muM H(2)O(2) significantly potentiated the release of IL-8 from the epithelial cells after stimulation with 10 microg/ml poly(I:C). Hydrogen Peroxide 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 19597128-5 2010 One hundred to 150 muM H(2)O(2) significantly potentiated the release of IL-8 from the epithelial cells after stimulation with 10 microg/ml poly(I:C). poly 140-144 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 19597128-6 2010 The H(2)O(2)-augmented IL-8 release was inhibited by treatment with N-acetylcysteine. Acetylcysteine 68-84 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 20517377-1 2010 Sodium was incorporated into Cu(In,Ga)Se(2) (CIGS) thin films by evaporating NaF before the second and third stages and after the third stage of CIGS deposition. Sodium 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 20092409-3 2010 We further observed that supplementation with H(2)S or an endogenous precursor of H(2)S (l-cysteine) in culture medium prevents IL-8 and MCP-1 secretion in high-glucose-treated human U937 monocytes. Hydrogen Sulfide 82-87 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 20092409-3 2010 We further observed that supplementation with H(2)S or an endogenous precursor of H(2)S (l-cysteine) in culture medium prevents IL-8 and MCP-1 secretion in high-glucose-treated human U937 monocytes. Cysteine 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 20304034-0 2010 Galactose specific adhesin of enteroaggregative E. coli induces IL-8 secretion via activation of MAPK and STAT-3 in INT-407 cells. Galactose 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 20188144-0 2010 Selenium supplementation attenuates procollagen-1 and interleukin-8 production in fat-loaded human C3A hepatoblastoma cells treated with TGFbeta1. Selenium 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 20188144-9 2010 CONCLUSIONS: Our data establish that both fat-loading and suboptimal selenium status enhance collagen and IL-8 production by C3A hepatocytes in response to TGFbeta1, possibly as part of an epithelial to mesenchymal transition. Selenium 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 20607488-3 2010 This study showed that ethanol extract of AJK interestingly suppressed the production and mRNA expression of TNF-alpha, IL-6 and IL-8, as important inflammatory cytokines. Ethanol 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 20304034-10 2010 Further, the adhesin induced IL-8 secretion was reduced in the presence of the inhibitors of MEK (PD098059), p38-MAPK (SB203580) and JAK (-2,-3)/STAT-3 pathway (AG490). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 98-106 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 20053132-5 2010 Copper stimulated cell proliferation and the expression of MMP-1 and IL-8 genes at the protein, mRNA, and promoter levels, indicating transcriptional regulation, without significantly altering TIMP-1. Copper 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 20304034-10 2010 Further, the adhesin induced IL-8 secretion was reduced in the presence of the inhibitors of MEK (PD098059), p38-MAPK (SB203580) and JAK (-2,-3)/STAT-3 pathway (AG490). SB 203580 119-127 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 20304034-11 2010 CONCLUSIONS: We propose that STAT-3 activation is quintessential for the galactose specific adhesin induced IL-8 secretion by INT-407 cells and must occur in concert with the activation of ERK1/2. Galactose 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 20053132-2 2010 Wound healing and skin aging are facilitated by matrixmetalloproteinases (MMP), which remodel the extracellular matrix, and interleukin-8 (IL-8), linked with copper. Copper 158-164 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 20053132-2 2010 Wound healing and skin aging are facilitated by matrixmetalloproteinases (MMP), which remodel the extracellular matrix, and interleukin-8 (IL-8), linked with copper. Copper 158-164 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 20053132-3 2010 This research investigated the mechanism to copper"s role in wound healing or skin aging by regulation of MMP-1 and IL-8 genes. Copper 44-50 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 20445007-7 2010 PAM stimulation also induced IL-1beta, IL-6, and IL-8. pam 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 20445007-10 2010 In contrast, delayed DEX addition significantly suppressed PAM-induced IL-1beta, IL-6, or IL-8 and also suppressed LPS-induced IL-1beta and IL-8. Dexamethasone 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 20445007-10 2010 In contrast, delayed DEX addition significantly suppressed PAM-induced IL-1beta, IL-6, or IL-8 and also suppressed LPS-induced IL-1beta and IL-8. Dexamethasone 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 20445007-10 2010 In contrast, delayed DEX addition significantly suppressed PAM-induced IL-1beta, IL-6, or IL-8 and also suppressed LPS-induced IL-1beta and IL-8. pam 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 20053132-6 2010 The research suggests that copper facilitates wound healing as well as skin aging via the induction of MMP-1 expression, with limiting MMP effect at the higher concentrations through enhanced IL-8 expression, which favors extracellular matrix deposition. Copper 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 20232292-8 2010 Ethanol-exposed macrophages developed enhanced interleukin 6 (IL6), IL8, and tumor necrosis factor alpha responses to lipopolysaccharide with time-dependent increases in histone acetylation that could be prevented by inhibition of ethanol metabolism. Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 21119886-6 2010 Here, we provide a view suggesting that caffeine could exert some of its effects by acting on several signaling complexes composed of HIF-1alpha/VEGF/IL-8 along with NO, TNF-alpha, IL1, and GHRH, among others. Caffeine 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 20107167-7 2010 RESULTS: Zymosan induced the release of IL-6 and IL-8 from corneal fibroblasts without affecting either the release of IL-1beta, IL-12, IP-10, or RANTES or the expression of ICAM-1 or VCAM-1. Zymosan 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 20091087-0 2010 Geniposide inhibits interleukin-6 and interleukin-8 production in lipopolysaccharide-induced human umbilical vein endothelial cells by blocking p38 and ERK1/2 signaling pathways. geniposide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 20091087-1 2010 OBJECTIVE: The aim of this study was to investigate the inhibitory effect of geniposide on lipopolysaccharide (LPS)-induced interleukin-6 (IL-6) and interleukin-8 (IL-8) production in human umbilical vein endothelial cells (HUVECs). geniposide 77-87 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 20091087-6 2010 RESULTS: Geniposide effectively inhibited LPS-induced expression of IL-6 and IL-8 in HUVECs at the transcription and translation levels. geniposide 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 20091087-9 2010 CONCLUSION: The results show that geniposide can inhibit LPS-induced IL-6 and IL-8 production in HUVECs by blocking p38 MAPK and ERK1/2 signaling pathways. geniposide 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 20635653-4 2010 RESULTS: The corrosion potential (E(corr)) and polarization resistance (R(p)) values of titanium alloy decreased with the increasing of NaF concentration, while the corrosion current density (I(corr)) values increased with the increasing of NaF concentration in acidic artificial saliva. Titanium 88-102 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 20635653-4 2010 RESULTS: The corrosion potential (E(corr)) and polarization resistance (R(p)) values of titanium alloy decreased with the increasing of NaF concentration, while the corrosion current density (I(corr)) values increased with the increasing of NaF concentration in acidic artificial saliva. Titanium 88-102 C-X-C motif chemokine ligand 8 Homo sapiens 241-244 20635653-7 2010 CONCLUSION: The fluoride ions have a negative influence on the corrosion resistance of Ti-12Zr alloy and Ti-6Al-4V alloy, especially in the acidic artificial saliva which contained over 0.1% NaF. Fluorides 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 191-194 20107167-9 2010 The zymosan-induced release of IL-6 and IL-8 was attenuated by inhibitors of ERK, p38, JNK, and NF-kappaB signaling. Zymosan 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 20107167-10 2010 CONCLUSIONS: Zymosan induces the release of IL-6 and IL-8 from human corneal fibroblasts in a manner dependent on MAPK and NF-kappaB signaling pathways. Zymosan 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 20302854-0 2010 Mycophenolic acid inhibits the phosphorylation of NF-kappaB and JNKs and causes a decrease in IL-8 release in H2O2-treated human renal proximal tubular cells. Mycophenolic Acid 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 20193726-10 2010 CONCLUSIONS: The incorporation of NaF 0.05% fluoride therapy to the cariogenic challenge was capable to recover the original microhardness of dentin at 50 and 100 microm with all the tested materials. Fluorides 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 19428234-10 2010 Moreover, tryptophan reduced the expression of the pro-inflammatory cytokines tumor necrosis factor-alpha, interleukin (IL)-6, interferon (IFN)-gamma, IL-12p40, IL-1beta and IL-17, as well as IL-8 and intracellular adhesion molecule-1, and resulted in increased expression of apoptosis initiators caspase-8 and Bax. Tryptophan 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 20181660-3 2010 Similar to PKR inhibitors, Hck inhibitor 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyramidine (PP2) suppressed p38 activation and p38-driven interleukin 8 (IL-8) expression in the U937 human monocyte cell line. 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyramidine 41-104 C-X-C motif chemokine ligand 8 Homo sapiens 152-165 20181660-3 2010 Similar to PKR inhibitors, Hck inhibitor 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyramidine (PP2) suppressed p38 activation and p38-driven interleukin 8 (IL-8) expression in the U937 human monocyte cell line. 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyramidine 41-104 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 19910110-2 2010 Phosphorylation of p65 at serine 276 is required for the expression of a subset of NF-kappaB regulated genes, including vascular cell adhesion molecule-1 (VCAM-1) and interleukin-8 (IL-8). Serine 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 19910110-2 2010 Phosphorylation of p65 at serine 276 is required for the expression of a subset of NF-kappaB regulated genes, including vascular cell adhesion molecule-1 (VCAM-1) and interleukin-8 (IL-8). Serine 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 20512931-6 2010 In contrast, inhibition of SHP-2 enzymatic activity (sodium stibogluconate) abrogated the increased ERK phosphorylation associated with integrin beta4 silencing in LPS-treated EC and attenuated the increases in levels of IL-6 and IL-8 in integrin-beta4-silenced EC. Antimony Sodium Gluconate 53-74 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 20494134-4 2010 Induction of IL-8 production by both alpha-lactalbumin and beta-lactoglobulin was higher than that by lactose and NDM; alpha-lactalbumin was a more potent inducer of IL-8 than beta-lactoglobulin and IL-1beta alone in both unstimulated and stimulated cells. Lactose 102-109 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 20200221-8 2010 Exposure to 4-OPA significantly elevated IL-8, IL-6, GM-CSF, and TNF-alpha while glutaraldehyde caused significant elevations in IL-6, IL-8, and TNF-alpha. 4-oxopentanal 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 20200221-8 2010 Exposure to 4-OPA significantly elevated IL-8, IL-6, GM-CSF, and TNF-alpha while glutaraldehyde caused significant elevations in IL-6, IL-8, and TNF-alpha. Glutaral 81-95 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 20200221-9 2010 IL-6 and IL-8 were also significantly elevated after exposure to diacetyl, glyoxal, and methyl glyoxal. Glyoxal 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 20200221-9 2010 IL-6 and IL-8 were also significantly elevated after exposure to diacetyl, glyoxal, and methyl glyoxal. Glyoxal 95-102 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 20302854-0 2010 Mycophenolic acid inhibits the phosphorylation of NF-kappaB and JNKs and causes a decrease in IL-8 release in H2O2-treated human renal proximal tubular cells. Hydrogen Peroxide 110-114 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 20302854-5 2010 Pre-incubation of the cells with mycophenolic acid (MPA) resulted in reduced phosphorylation of both JNKs and NF-kappaB, and reduced IL-8 release in H(2)O(2)-stimulated HK-2 cells. Mycophenolic Acid 33-50 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 20181930-8 2010 In addition, OxLDL treatment stimulated ROCK2 catalytic activity, and ROCK2 inhibition attenuated NF-kappaB activation and IL-8 production resulting from OxLDL activation of LOX-1. oxldl 154-159 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 20050751-11 2010 The presence of fluoride in artificial saliva was detrimental to the corrosion resistance of the test NiTi archwires, especially at a 0.5% NaF concentration. Fluorides 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 20406839-10 2010 Moreover, decreased microvessel density was observed, possibly secondary to increased expression of the antiangiogenic factor CXCL10 and decreased proangiogenic interleukin-8 cytokine in response to TRAIL/doxorubicin combination, as was also observed in vitro. Doxorubicin 205-216 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 20423350-5 2010 KEY RESULTS: Pre-incubation with beta(2)-adrenoceptor agonists (salbutamol, salmeterol, formoterol) augmented the release and mRNA expression of IL-6 and IL-8 induced by IL-1beta and IL-1beta plus histamine, whereas NF-kappaB-dependent transcription was significantly repressed, and AP-1-dependent transcription was unaffected. Albuterol 64-74 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20423350-5 2010 KEY RESULTS: Pre-incubation with beta(2)-adrenoceptor agonists (salbutamol, salmeterol, formoterol) augmented the release and mRNA expression of IL-6 and IL-8 induced by IL-1beta and IL-1beta plus histamine, whereas NF-kappaB-dependent transcription was significantly repressed, and AP-1-dependent transcription was unaffected. Salmeterol Xinafoate 76-86 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20423350-5 2010 KEY RESULTS: Pre-incubation with beta(2)-adrenoceptor agonists (salbutamol, salmeterol, formoterol) augmented the release and mRNA expression of IL-6 and IL-8 induced by IL-1beta and IL-1beta plus histamine, whereas NF-kappaB-dependent transcription was significantly repressed, and AP-1-dependent transcription was unaffected. Formoterol Fumarate 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 20423350-8 2010 Addition of dexamethasone with salmeterol repressed IL-6 and IL-8 release to levels that were similar to the repression achieved in the absence of salmeterol. Dexamethasone 12-25 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 20423350-8 2010 Addition of dexamethasone with salmeterol repressed IL-6 and IL-8 release to levels that were similar to the repression achieved in the absence of salmeterol. Salmeterol Xinafoate 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 20423350-9 2010 IL-6 release was enhanced when salmeterol was added before, concurrently or after IL-1beta plus histamine stimulation, whereas IL-8 release was only enhanced by salmeterol addition prior to stimulation. Salmeterol Xinafoate 161-171 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 20388003-8 2010 Budesonide significantly attenuated the release and expression of IL-6 and IL-8 after exposure. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 19788440-15 2010 Plasma interleukin-8 levels were significantly lower in the sivelestat-treated group than in the control group on POD 3 (P= 0.040). sivelestat 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 7-20 20388003-11 2010 Budesonide reduced IL-6 and IL-8 production and enhanced expression of TLR2 in PBECs only in the presence of a proinflammatory stimulus. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 20194598-7 2010 We observed that epithelial production of interleukin-8 (IL-8) and IL-6 in response to bacterial stimulation was significantly inhibited in the presence of CS (P < 0.001 for inhibition by either CSC or CSE). Cesium 156-158 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 20019359-8 2010 CXCL8 secretion by LPS-treated IPE was dependent on CD14 and TLR4. ipe 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 20194598-7 2010 We observed that epithelial production of interleukin-8 (IL-8) and IL-6 in response to bacterial stimulation was significantly inhibited in the presence of CS (P < 0.001 for inhibition by either CSC or CSE). Cesium 156-158 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 20164300-5 2010 Our results showed that butrin, isobutrin, and butein significantly reduced the phorbol 12-myristate 13-acetate and calcium ionophore A23187-induced inflammatory gene expression and production of TNF-alpha, IL-6, and IL-8 in HMC-1 cells by inhibiting the activation of NF-kappaB. Tetradecanoylphorbol Acetate 80-111 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 20187772-9 2010 Muscle mRNA expression for IL-8 (6.4-fold), MCP-1 (4.7-fold), and IL-6 (7.3-fold) increased substantially after carbohydrate ingestion. Carbohydrates 112-124 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 20002790-10 2010 NOD2 activation with MurNAc-l-Ala-d-isoGln (MDP) resulted in interleukin-8 secretion, CD62 ligand down-regulation, CD11b up-regulation and increased migration towards an inflammatory stimulus. Acetylmuramyl-Alanyl-Isoglutamine 21-42 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 20002790-10 2010 NOD2 activation with MurNAc-l-Ala-d-isoGln (MDP) resulted in interleukin-8 secretion, CD62 ligand down-regulation, CD11b up-regulation and increased migration towards an inflammatory stimulus. Acetylmuramyl-Alanyl-Isoglutamine 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 20164300-0 2010 Butrin, isobutrin, and butein from medicinal plant Butea monosperma selectively inhibit nuclear factor-kappaB in activated human mast cells: suppression of tumor necrosis factor-alpha, interleukin (IL)-6, and IL-8. butrin 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 20164300-5 2010 Our results showed that butrin, isobutrin, and butein significantly reduced the phorbol 12-myristate 13-acetate and calcium ionophore A23187-induced inflammatory gene expression and production of TNF-alpha, IL-6, and IL-8 in HMC-1 cells by inhibiting the activation of NF-kappaB. Calcium 116-123 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 20164300-5 2010 Our results showed that butrin, isobutrin, and butein significantly reduced the phorbol 12-myristate 13-acetate and calcium ionophore A23187-induced inflammatory gene expression and production of TNF-alpha, IL-6, and IL-8 in HMC-1 cells by inhibiting the activation of NF-kappaB. Calcimycin 134-140 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 20164300-0 2010 Butrin, isobutrin, and butein from medicinal plant Butea monosperma selectively inhibit nuclear factor-kappaB in activated human mast cells: suppression of tumor necrosis factor-alpha, interleukin (IL)-6, and IL-8. isobutrin 8-17 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 20019678-7 2010 Fasting glucose related to VAT expression of TNFalpha, MIP, serum amyloid A (SAA), IL-1alpha, IL-1beta, IL-8, and IL-8 receptor. Glucose 8-15 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 20164300-0 2010 Butrin, isobutrin, and butein from medicinal plant Butea monosperma selectively inhibit nuclear factor-kappaB in activated human mast cells: suppression of tumor necrosis factor-alpha, interleukin (IL)-6, and IL-8. butein 23-29 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 20164300-5 2010 Our results showed that butrin, isobutrin, and butein significantly reduced the phorbol 12-myristate 13-acetate and calcium ionophore A23187-induced inflammatory gene expression and production of TNF-alpha, IL-6, and IL-8 in HMC-1 cells by inhibiting the activation of NF-kappaB. butrin 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 20164300-5 2010 Our results showed that butrin, isobutrin, and butein significantly reduced the phorbol 12-myristate 13-acetate and calcium ionophore A23187-induced inflammatory gene expression and production of TNF-alpha, IL-6, and IL-8 in HMC-1 cells by inhibiting the activation of NF-kappaB. isobutrin 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 20164300-5 2010 Our results showed that butrin, isobutrin, and butein significantly reduced the phorbol 12-myristate 13-acetate and calcium ionophore A23187-induced inflammatory gene expression and production of TNF-alpha, IL-6, and IL-8 in HMC-1 cells by inhibiting the activation of NF-kappaB. butein 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 20639712-9 2010 The inflammatory biomarkers, erythrocyte sedimentation rate, and interleukin-8 decreased after supplementation with n-3 FA and erythrocyte sedimentation rate increased after supplementation with n-6 FA. Fatty Acids, Omega-3 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 20019678-7 2010 Fasting glucose related to VAT expression of TNFalpha, MIP, serum amyloid A (SAA), IL-1alpha, IL-1beta, IL-8, and IL-8 receptor. Glucose 8-15 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 20383325-9 2010 baumannii lipopolysaccharide stimulated IL-8 release by A549 cells and sCD14 facilitated the recognition of the lipopolysaccharide. baumannii lipopolysaccharide 0-28 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 20084405-6 2010 To avoid dilution effects and to the standardize samples, urinary levels of IL-6 and IL-8 were expressed as the ratio of cytokine to urinary creatinine (pg/mg). Creatinine 141-151 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 20176036-9 2010 In this study, we demonstrated that the up-regulated expressions of IL-8 or PGE(2) in Streptococci or PAMP-stimulated HDPF were inhibited by catechins, (-)-epicatechin gallate (ECG) and (-)-epigallocatechin gallate (EGCG). Catechin 141-150 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20176036-9 2010 In this study, we demonstrated that the up-regulated expressions of IL-8 or PGE(2) in Streptococci or PAMP-stimulated HDPF were inhibited by catechins, (-)-epicatechin gallate (ECG) and (-)-epigallocatechin gallate (EGCG). epicatechin gallate 152-175 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20176036-9 2010 In this study, we demonstrated that the up-regulated expressions of IL-8 or PGE(2) in Streptococci or PAMP-stimulated HDPF were inhibited by catechins, (-)-epicatechin gallate (ECG) and (-)-epigallocatechin gallate (EGCG). epicatechin gallate 177-180 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20176036-9 2010 In this study, we demonstrated that the up-regulated expressions of IL-8 or PGE(2) in Streptococci or PAMP-stimulated HDPF were inhibited by catechins, (-)-epicatechin gallate (ECG) and (-)-epigallocatechin gallate (EGCG). epigallocatechin gallate 186-214 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20176036-9 2010 In this study, we demonstrated that the up-regulated expressions of IL-8 or PGE(2) in Streptococci or PAMP-stimulated HDPF were inhibited by catechins, (-)-epicatechin gallate (ECG) and (-)-epigallocatechin gallate (EGCG). epigallocatechin gallate 216-220 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20084046-5 2010 Interleukin 6 mRNA expression in cultured islets, as well as IL-6, IL-8, and granulocyte-macrophage colony-stimulating factor released into the medium, was significantly reduced by adding SD-282. indole-5-carboxamide 188-194 C-X-C motif chemokine ligand 8 Homo sapiens 67-125 20220108-6 2010 Arachidonic acid activated neutrophils to produce IL-8, which was completely inhibited by NS398. Arachidonic Acid 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 20222014-8 2010 In addition, AC-treated MSC secreted interleukin (IL)-8, monocyte chemoattractant protein-1, and RANTES, which might induce chemotaxis of CD4+ T cells to the inflamed joints. Charcoal 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 37-55 20218918-5 2010 RESULTS: In the patients with PTF, maximum mean plasma IL-6 and IL-8 values were found, respectively at 24 h (45.12 pg/mL) and 6 hours (21.7 pg/mL) postoperatively. Benzyl methyl sulfide 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 20218918-6 2010 Whereas, in the patients with FCF, it was respectively, at 12 h (33.1 pg/mL) and 6 h (17.0 pg/mL), for IL-6 and IL-8 post operatively. 3-[(1e,7e)-8-(2,6-Dioxo-1,2,3,6-Tetrahydropyrimidin-4-Yl)-3,6-Dioxa-2,7-Diazaocta-1,7-Dien-1-Yl]benzoic Acid 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 19597830-4 2010 Moreover, as we previously showed that epigallocatechin-3-gallate (EGCG) reduces VEGF and CXCL8/IL-8 secretion in TNFalpha-activated NHKs, we also tested its effect in association with GBE. epigallocatechin gallate 39-65 C-X-C motif chemokine ligand 8 Homo sapiens 90-95 19597830-4 2010 Moreover, as we previously showed that epigallocatechin-3-gallate (EGCG) reduces VEGF and CXCL8/IL-8 secretion in TNFalpha-activated NHKs, we also tested its effect in association with GBE. epigallocatechin gallate 39-65 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 19597830-4 2010 Moreover, as we previously showed that epigallocatechin-3-gallate (EGCG) reduces VEGF and CXCL8/IL-8 secretion in TNFalpha-activated NHKs, we also tested its effect in association with GBE. epigallocatechin gallate 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 90-95 19597830-4 2010 Moreover, as we previously showed that epigallocatechin-3-gallate (EGCG) reduces VEGF and CXCL8/IL-8 secretion in TNFalpha-activated NHKs, we also tested its effect in association with GBE. epigallocatechin gallate 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 19597830-6 2010 In association with EGCG, GBE down-regulated VEGF and CXCL8/IL-8 levels in a cumulative manner in TNFalpha-stimulated NHKs. epigallocatechin gallate 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 54-59 19597830-6 2010 In association with EGCG, GBE down-regulated VEGF and CXCL8/IL-8 levels in a cumulative manner in TNFalpha-stimulated NHKs. epigallocatechin gallate 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 19649704-7 2010 Thus, our study clearly demonstrated that doxorubicin-mediated cell death is obtained through expression of IL-8. Doxorubicin 42-53 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 20110572-4 2010 METHODS AND RESULTS: THP-1 monocytes exposed to 100 micromol/L SFA in vitro for 16 hours followed by 1 ng/mL lipopolysaccharide demonstrated enhanced IL-6 and IL-8 mRNA and protein expression (approximately 3-fold higher than the sum of individual responses to SFA and lipopolysaccharide). Fatty Acids 63-66 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 20233217-7 2010 In all but one mutation, the changes observed on antagonist affinity were matched with effects on inhibition of interleukin-8-stimulated [(35)S]GTPgammaS binding. Guanosine 5'-O-(3-Thiotriphosphate) 144-153 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 19649704-0 2010 Late phase activation of nuclear transcription factor kappaB by doxorubicin is mediated by interleukin-8 and induction of apoptosis via FasL. Doxorubicin 64-75 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 19649704-4 2010 Further induction of NF-kappaB was observed through interleukin 8 (IL-8), expressed by doxorubicin treatment. Doxorubicin 87-98 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 19649704-4 2010 Further induction of NF-kappaB was observed through interleukin 8 (IL-8), expressed by doxorubicin treatment. Doxorubicin 87-98 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 19649704-8 2010 IL-8-mediated calcification is required for enhancement of doxorubicin-mediated cell death. Doxorubicin 59-70 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19649704-6 2010 Anti-IL-8 or -FasL antibody, dominant negative TRAF6 (TRAF6-DN), or TRAF6 binding peptide (TRAF6-BP) inhibited doxorubicin-mediated late phase induction of NF-kappaB and diminished cell death. Doxorubicin 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 19399612-6 2010 Collectively, MG132 blocked PaCa-derived VEGF and IL-8 production through inhibition of NF-kappaB activity. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 20397810-9 2010 IS-SCGB1A1/IL8 levels were also inversely associated with nitrogen slope [r = -0.52, p < 0.001] and HRCT SA score [r = -0.51, p < 0.001]. Nitrogen 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 20397810-11 2010 The SCGB1A1/IL8 ratio measured in sputum is a potentially valuable biomarker for non-invasive assessment of SA remodelling in smokers. sa 108-110 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 19399612-8 2010 Our studies show that MG132, a proteasome inhibitor, significantly blocked pancreatic-cancer-associated angiogenesis through inhibition of NF-kappaB and NF-kappaB-dependent proangiogenic gene products VEGF and IL-8. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 19840967-9 2010 At 10(-9) and 10(-10) M, GW-A, that had no direct effects, increased the inhibitory activity of dexamethasone (10(-8) and 10( -6) M) on LPS-induced IL-8 release in PBMCs from severe asthma. Dexamethasone 96-109 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 20487003-6 2010 The presence of EGCG and ECG significantly reduced, in a concentration-dependent manner, the expression of IL-6 and IL-8 in dental pulp cells exposed to LPS or PG. epigallocatechin gallate 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 20487003-6 2010 The presence of EGCG and ECG significantly reduced, in a concentration-dependent manner, the expression of IL-6 and IL-8 in dental pulp cells exposed to LPS or PG. epicatechin gallate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 19559500-7 2010 RESULTS: Lidocaine inhibited spontaneous and TNF-alpha induced secretion of IL-8 and IP-10. Lidocaine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 20119897-8 2010 RESULTS: Treatment of human islets with RvE1 (500 nM) for 24 h reduced LPS-induced increase in mRNA and protein levels of selected pro-inflammatory markers (IL-8, MCP-1, and TF). lps 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 19559500-14 2010 CONCLUSION: Lidocaine inhibits IL-8 and IP-10 secretion from intestinal cells. Lidocaine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 20198307-0 2010 Involvement of capsular polysaccharide via a TLR2/NF-kappaB pathway in Vibrio vulnificus-induced IL-8 secretion of human intestinal epithelial cells. capsular polysaccharide 15-38 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 20138154-4 2010 Hirsutenone, dexamethasone, ERK inhibitor or Bay 11-7085 (an inhibitor of NF-kappaB activation) reduced the lipopolysaccharide-induced production of cytokines IL-1beta and IL-8, and the chemokine CCL17. hirsutenone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 20138154-4 2010 Hirsutenone, dexamethasone, ERK inhibitor or Bay 11-7085 (an inhibitor of NF-kappaB activation) reduced the lipopolysaccharide-induced production of cytokines IL-1beta and IL-8, and the chemokine CCL17. Dexamethasone 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 20138154-4 2010 Hirsutenone, dexamethasone, ERK inhibitor or Bay 11-7085 (an inhibitor of NF-kappaB activation) reduced the lipopolysaccharide-induced production of cytokines IL-1beta and IL-8, and the chemokine CCL17. BAY 11-7085 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 20646342-9 2010 NTHi was able to potentiate the stimulatory actions of TNF-alpha on caspase-3 expression and, to a lesser extent, on IL-8 secretion. nthi 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 20198307-3 2010 The CPS-defective wbpP mutant induced significantly lower levels of IL-8 production, IL-8 gene promoter activation and NF-kappaB activity in INT-407 cells than was noted with the wild-type or wbpP-complemented V. vulnificus. cps 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20198307-3 2010 The CPS-defective wbpP mutant induced significantly lower levels of IL-8 production, IL-8 gene promoter activation and NF-kappaB activity in INT-407 cells than was noted with the wild-type or wbpP-complemented V. vulnificus. cps 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 20198307-6 2010 Furthermore, purified V. vulnificus CPS was found to significantly induce IL-8 production and NF-kappaB activation, both of which were inhibited upon the addition of the anti-TLR2 antibody. cps 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 20198307-7 2010 Taken together, these results demonstrate that V. vulnificus capsular polysaccharide is involved in the induction of IL-8 production of human intestinal epithelial cells via a TLR2/NF-kappaB-dependent pathway. vulnificus capsular polysaccharide 50-84 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 20194723-8 2010 Taken together, our results suggest that BLT2-Nox1-reactive oxygen species-dependent pathway plays a role in promoting the secretion of IL-8 from human mast cells in response to the proinflammatory cytokine IL-1beta, thus contributing to angiogenesis. reactive 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 20194723-8 2010 Taken together, our results suggest that BLT2-Nox1-reactive oxygen species-dependent pathway plays a role in promoting the secretion of IL-8 from human mast cells in response to the proinflammatory cytokine IL-1beta, thus contributing to angiogenesis. oxygen species 60-74 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 20204339-7 2010 Using receiver operating characteristics curve analysis, we found that the adjusted IL-8 level of 6.2 pg/mg creatinine can reach a sensitivity of 90% and specificity of 68% to detect urolithiasis. Creatinine 108-118 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 20053934-7 2010 In addition, chromatin immunoprecipitation assays revealed that the DNA binding of NF-kappaB (p65) to il-8 promoter in RSF was induced after TNFalpha stimulation and that, upon CHPD treatment to RSF for 1 h, the NF-kappaB binding to il-8 promoter was significantly decreased. (3r,3as,6ar)-Hexahydrofuro[2,3-B]furan-3-Ol 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 20053934-7 2010 In addition, chromatin immunoprecipitation assays revealed that the DNA binding of NF-kappaB (p65) to il-8 promoter in RSF was induced after TNFalpha stimulation and that, upon CHPD treatment to RSF for 1 h, the NF-kappaB binding to il-8 promoter was significantly decreased. (3r,3as,6ar)-Hexahydrofuro[2,3-B]furan-3-Ol 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 20308455-1 2010 PURPOSE: To evaluate the sensitivity of fluorine 18-labeled sodium fluoride ((18)F-NaF) positron emission tomography (PET) for assessment of skeletal trauma in pediatric patients suspected of having been abused and to compare the diagnostic performance of this examination with that of high-detail skeletal survey. Fluorine 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 20308455-1 2010 PURPOSE: To evaluate the sensitivity of fluorine 18-labeled sodium fluoride ((18)F-NaF) positron emission tomography (PET) for assessment of skeletal trauma in pediatric patients suspected of having been abused and to compare the diagnostic performance of this examination with that of high-detail skeletal survey. Sodium Fluoride 60-75 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 20660970-1 2010 BACKGROUND: This study was designed to compare 2% sodium fluoride (NaF) iontophoresis with other cavity liners. Sodium Fluoride 50-65 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 20089808-7 2010 An aminopyridine-based JNK inhibitor, N-(4-amino-5-cyano-6-ethoxypyridin-2-yl)-2-(2,5-dimethoxyphenyl)acetamide (JNK inhibitor VIII), inhibited phosphorylation of a JNK substrate c-Jun but did not have any effect on IL-6, IL-8, or COX-2 expression. Aminopyridines 3-16 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 19898747-5 2010 Further, pretreatment of these cells with the highly specific MEK inhibitor (PD 098059), the JNK inhibitor (SP 600125), and the p38MAPK inhibitor (SB 203580) resulted in inhibition of the IL-8 secretion by EAEC (wild type as well as plasmid cured)-infected INT-407 cells. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 77-86 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 19898747-5 2010 Further, pretreatment of these cells with the highly specific MEK inhibitor (PD 098059), the JNK inhibitor (SP 600125), and the p38MAPK inhibitor (SB 203580) resulted in inhibition of the IL-8 secretion by EAEC (wild type as well as plasmid cured)-infected INT-407 cells. pyrazolanthrone 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 19898747-5 2010 Further, pretreatment of these cells with the highly specific MEK inhibitor (PD 098059), the JNK inhibitor (SP 600125), and the p38MAPK inhibitor (SB 203580) resulted in inhibition of the IL-8 secretion by EAEC (wild type as well as plasmid cured)-infected INT-407 cells. SB 203580 147-156 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 19919624-10 2010 tumor necrosis factor-alpha (P < 0.04) and IL-8 were less (P < 0.001) in the plasma from the PVS group, while IL-6 and IL-8 were less (P < 0.04) in the lung tissue from ventilated lungs in the PVS group. 2-(phenylsulfonyl)ethanethiol 99-102 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19919624-10 2010 tumor necrosis factor-alpha (P < 0.04) and IL-8 were less (P < 0.001) in the plasma from the PVS group, while IL-6 and IL-8 were less (P < 0.04) in the lung tissue from ventilated lungs in the PVS group. 2-(phenylsulfonyl)ethanethiol 99-102 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 19733855-2 2010 The aim of this study was to determine if GSA induces chemokine, particularly CXCL8 (IL-8), and to determine intracellular signaling pathways activated by GSA in vascular smooth muscle cells (VSMCs). gsa 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 78-83 20366434-1 2010 X-ray reflectometry reveals atomic layering at a liquid-liquid interface--mercury in a 0.01 M NaF solution. Mercury 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 20080229-3 2010 The in vitro effect of saponins on LPS-induced IL-8 and TNF-alpha mRNA level (by quantitative RT-PCR) and protein release (by ELISA) was evaluated in human THP-1 macrophages. Saponins 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 20080229-4 2010 We found that compounds 1 (repandoside), 2 (deglucocyclamin) and 4 (anagalloside B) at 100 microM inhibited the LPS-induced IL-8 and TNF-alpha expressions. repandoside 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 20080229-4 2010 We found that compounds 1 (repandoside), 2 (deglucocyclamin) and 4 (anagalloside B) at 100 microM inhibited the LPS-induced IL-8 and TNF-alpha expressions. Deglucocyclamin 44-59 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 20080229-4 2010 We found that compounds 1 (repandoside), 2 (deglucocyclamin) and 4 (anagalloside B) at 100 microM inhibited the LPS-induced IL-8 and TNF-alpha expressions. anagalloside B 68-82 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 20093183-8 2010 CSE (2.5-10%) induced upregulation of IL-6, IL-8 and Ang-2, and decreased Ang-1 expression in parallel to apoptosis which were partially suppressed by sildenafil, 8-Br-cGMP, DPI and NAC. Sildenafil Citrate 151-161 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 20064484-2 2010 Human neutrophils produced IL-8 and TNF-alpha in response to stimulation with TLR agonists such as LPS and N-palmitoyl-S-[2,3-bis(palmitoyloxy)-(2RS)-propyl]-(R)-cysteinyl-seryl-(lysyl)(3)-lysine. n-palmitoyl-s-[2,3-bis(palmitoyloxy)-(2rs)-propyl]-(r)-cysteinyl-seryl-(lysyl)(3)-lysine 107-195 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 20214814-5 2010 We found elevated levels of PGE2 and CXCL8 in subjects with PDAC, and chronic pancreatitis. pdac 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 37-42 20185670-0 2010 Ketamine inhibits transcription factors activator protein 1 and nuclear factor-kappaB, interleukin-8 production, as well as CD11b and CD16 expression: studies in human leukocytes and leukocytic cell lines. Ketamine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 87-100 20185670-6 2010 Ketamine"s effect on interleukin-8 production was assessed in a whole blood assay. Ketamine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 20185670-9 2010 Ketamine also reduced interleukin-8 production in whole blood and expression of CD11b and CD16 on neutrophils. Ketamine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 19733855-2 2010 The aim of this study was to determine if GSA induces chemokine, particularly CXCL8 (IL-8), and to determine intracellular signaling pathways activated by GSA in vascular smooth muscle cells (VSMCs). gsa 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 19733855-4 2010 GSA-induced promoter activation of the IL-8 gene was suppressed by dominant-negative mutants of TLR-4, MyD88, and TRIF, but not by a dominant-negative form of TLR-2. gsa 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 19733855-5 2010 In addition, IL-8 up-regulation in response to GSA was inhibited by resveratrol, curcumin, diphenyleneiodium, U0126, and SB202190. gsa 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19733855-5 2010 In addition, IL-8 up-regulation in response to GSA was inhibited by resveratrol, curcumin, diphenyleneiodium, U0126, and SB202190. Resveratrol 68-79 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19733855-5 2010 In addition, IL-8 up-regulation in response to GSA was inhibited by resveratrol, curcumin, diphenyleneiodium, U0126, and SB202190. Curcumin 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19874800-7 2010 Moreover, the overproduction of IL-8 was associated with an enhanced increase in the translocation of NF-kappaB and an enhanced decrease in glutathione levels. Glutathione 140-151 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 19733855-5 2010 In addition, IL-8 up-regulation in response to GSA was inhibited by resveratrol, curcumin, diphenyleneiodium, U0126, and SB202190. diphenyleneiodium 91-108 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19874800-9 2010 In conclusion, CSM exposure of macrophages up-regulates the expression and the production of IL-8 via reactive oxygen species and NF-kappaB activation. Reactive Oxygen Species 102-125 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 19733855-5 2010 In addition, IL-8 up-regulation in response to GSA was inhibited by resveratrol, curcumin, diphenyleneiodium, U0126, and SB202190. U 0126 110-115 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19733855-5 2010 In addition, IL-8 up-regulation in response to GSA was inhibited by resveratrol, curcumin, diphenyleneiodium, U0126, and SB202190. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19733855-8 2010 This study suggests that GSA induces expression of IL-8 in VSMCs and that TLR-4, mitogen-activated protein kinases, NF-kappaB, and NADPH oxidase are involved in that process. gsa 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 20397120-8 2010 RESULTS: CO (2), but not hypoxia, induced a significant reduction in the release of TNF-alpha and IL-8 as well as a significant increase in the release of IL-10 and IL-1 beta within the first 4 h after incubation. co (2) 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 20356455-5 2010 However, dsCpGDNA encapsulated with lipofectin induced IL-8 promoter activation, HLA-DRA expression, and IL-8 expression in a CG sequence- independent manner. 1,2-dielaidoylphosphatidylethanolamine 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 20356455-5 2010 However, dsCpGDNA encapsulated with lipofectin induced IL-8 promoter activation, HLA-DRA expression, and IL-8 expression in a CG sequence- independent manner. 1,2-dielaidoylphosphatidylethanolamine 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 19185976-3 2010 In vitro, Mox-LDL triggered the inflammatory response by increasing the release of both interleukin 8 (IL-8) and tumor necrosis factor alpha (TNF-alpha) by endothelial cells (ECs) and monocytes respectively. mox-ldl 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 19185976-3 2010 In vitro, Mox-LDL triggered the inflammatory response by increasing the release of both interleukin 8 (IL-8) and tumor necrosis factor alpha (TNF-alpha) by endothelial cells (ECs) and monocytes respectively. mox-ldl 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 19185976-9 2010 RESULTS AND LIMITATIONS: Two-way ANOVA analysis showed that TNF-alpha alone (p<0.001) or Mox-LDL alone (p<0.001) increased IL-8 production. mox-ldl 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 19185976-11 2010 Tadalafil in combination with Mox-LDL and TNF-alpha showed a decrease of IL-8 (p<0.05) compared with sildenafil and vardenafil. Tadalafil 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 20008399-0 2010 Signal mechanisms of vascular endothelial growth factor and interleukin-8 in ovarian hyperstimulation syndrome: dopamine targets their common pathways. Dopamine 112-120 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 19185976-11 2010 Tadalafil in combination with Mox-LDL and TNF-alpha showed a decrease of IL-8 (p<0.05) compared with sildenafil and vardenafil. MOX 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 20008399-13 2010 Dopamine may block VEGF- and IL-8-induced endothelial permeability by inhibiting common VEGFR-2 dependent signals. Dopamine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 20118277-6 2010 Elevated levels of intracellular reactive oxygen species triggered the production of IL-8 as well as proinflammatory cytokines, such as TNF-alpha and IL-6. Reactive Oxygen Species 33-56 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 19259778-0 2010 Paricalcitol reduces basal and lipopolysaccharide-induced (LPS) TNF-alpha and IL-8 production by human peripheral blood mononuclear cells. paricalcitol 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 19259778-10 2010 The effect of paricalcitol on IL-8 production was more profound. paricalcitol 14-26 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 19259778-11 2010 Basal IL-8 concentration (1926 +/- 455 pg/ml) was reduced by paricalcitol (1273 +/- 472 pg/ml). paricalcitol 61-73 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 19259778-13 2010 CONCLUSION: The in vitro inhibition of transforming growth factor alpha and interleukin 8 by paricalcitol confirms the immunomodulatory properties of this vitamin D analogue. paricalcitol 93-105 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 19259778-13 2010 CONCLUSION: The in vitro inhibition of transforming growth factor alpha and interleukin 8 by paricalcitol confirms the immunomodulatory properties of this vitamin D analogue. Vitamin D 155-164 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 20470276-9 2010 Iron induced significant increase in plasma malondialdehyde and IL-8 in monocytes, but had no effect on total antioxidant capacity, CD11b/CD18 expression, plasma IL-8, vWF and sICAM-1. Iron 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 19815061-7 2010 ROS also triggered pro-inflammatory responses in cultured T98G cells, which were demonstrated by the increased gene expression and protein levels of IL-6 and IL-8. ros 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 20184737-7 2010 A seemingly contradictory correlation was found between low IL-8 serum levels and a need for a PEG tube. Polyethylene Glycols 95-98 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 20170497-17 2010 In general, treatment with silver-containing solutions resulted in decreased TNF-alpha and IL-8 expression, with increased IL-4, EGF, KGF, and KGF-2 expression. Silver 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 20187163-4 2010 Images of vials containing different concentrations of sodium fluoride (NaF) were converted to units of moles by reference to precalibrated synthetically injected voxels. Sodium Fluoride 55-70 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 22966296-0 2010 Down-regulation of IL-6, IL-8, TNF-alpha and IL-1beta by glucosamine in HaCaT cells, but not in the presence of TNF-alpha There is considerable evidence that glucosamine exerts an inhibitory effect on inflammatory cytokine expression in cells. Glucosamine 57-68 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 22966296-0 2010 Down-regulation of IL-6, IL-8, TNF-alpha and IL-1beta by glucosamine in HaCaT cells, but not in the presence of TNF-alpha There is considerable evidence that glucosamine exerts an inhibitory effect on inflammatory cytokine expression in cells. Glucosamine 158-169 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 22966296-5 2010 Our data showed that the expression of IL-6, IL-8, TNF-alpha and IL-1beta was decreased by glucosamine treatment in the HaCaT cells. Glucosamine 91-102 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 22966296-7 2010 Notably, curcumin induced an increased expression of IL-8 and IL-1beta in the HaCaT cells, but not that of IL-6 and TNF-alpha. Curcumin 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 22966296-8 2010 On the other hand, curcumin attenuated the expression of IL-6 and IL-8 in the TNF-alpha-treated HaCaT cells. Curcumin 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 22966296-9 2010 Our data indicated that glucosamine induced the down-regulation of IL-6, IL-8, TNF-alpha and IL-1beta expression in the HaCaT cells. Glucosamine 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 19655299-7 2010 Addition of ROC at different concentrations together with IFN-gamma and histamine induced a dose-dependent inhibition of ICAM-1 expression and MCP-1 and IL-8 release. Saquinavir 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 19655299-7 2010 Addition of ROC at different concentrations together with IFN-gamma and histamine induced a dose-dependent inhibition of ICAM-1 expression and MCP-1 and IL-8 release. Histamine 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 20052681-6 2010 By this method, 4-azido-L-phenylalanine was incorporated into human interleukin-8 at a specific site. 4-azidophenylalanine 16-39 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 20506652-8 2010 The RT-PCR verified the mRNA expression of IL-6 and IL-8 was up-regulated until 48 h after treatment with paraquat. Paraquat 106-114 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 20054232-4 2010 The reduced adhesion by GFW correlated with the suppressed expression of MCP-1 and IL-8, the major IBD-associated chemokines. ethyl 2-[4-[4-(3-methylbutylsulfamoyl)phenyl]-1,3-thiazol-2-yl]ethanoate 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 20054232-9 2010 The results suggest that GFW ameliorates colon inflammation by suppressing production of TNF-alpha as well as its signaling through NF-kappaB leading to the expression of inflammatory chemokines, MCP-1 and IL-8. ethyl 2-[4-[4-(3-methylbutylsulfamoyl)phenyl]-1,3-thiazol-2-yl]ethanoate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 20102702-5 2010 Surprisingly, the variant with deletion of amino acids 220-320 (FliCDelta220-320) induced higher production of IL-8, MCP-1, and TNF-alpha, and showed higher mucosal adjuvancy than full-length FliC flagellin. flicdelta220 64-76 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 20102702-5 2010 Surprisingly, the variant with deletion of amino acids 220-320 (FliCDelta220-320) induced higher production of IL-8, MCP-1, and TNF-alpha, and showed higher mucosal adjuvancy than full-length FliC flagellin. flic flagellin 192-206 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 20083671-6 2010 In monocytes, UDP, but not leukotriene D(4), induced IL-8 production that was significantly inhibited by both drugs at micromolar concentrations. Uridine Diphosphate 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 19647363-7 2010 Treatment of the cells with curcumin inhibited LPA-induced IL-6 and IL-8 secretion and STAT3 phosphorylation, leading to blocked ovarian cancer cell motility. Curcumin 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20140095-9 2010 Correspondingly, the interaction of Abeta(1-40) with HFA-GSLs is strongly inhibited by NaF, an efficient competitor of H-bond formation. Glycosphingolipids 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 19945446-5 2010 These effects are ascribable to the fluoride content/release of glass powders, since they were mimicked by NaF solutions and were prevented by dimethyl sulfoxide and tempol (two radical scavengers), by superoxide dismutase (a superoxide scavenger), and by glutathione (the most important intracellular antioxidant molecule), but not by apocynin (an inhibitor of NADPH oxidase). Fluorides 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 19945446-6 2010 The presence of fluoride-containing glasses and NaF caused also the generation of reactive oxygen species, which was prevented by superoxide dismutase and catalase. Reactive Oxygen Species 82-105 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 19647363-7 2010 Treatment of the cells with curcumin inhibited LPA-induced IL-6 and IL-8 secretion and STAT3 phosphorylation, leading to blocked ovarian cancer cell motility. lysophosphatidic acid 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20103651-0 2010 Interleukin-8 mediates resistance to antiangiogenic agent sunitinib in renal cell carcinoma. Sunitinib 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 19884117-7 2010 From receptor binding analysis AAL-glycan was found to bind IL-8 receptors especially CXCR2 directly and such binding could be blocked by 3"- or 2"-fucosyllactose. aal-glycan 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 20103651-6 2010 Notably, escape coincided with increased secretion of interleukin-8 (IL-8) from tumors into the plasma, and coadministration of an IL-8 neutralizing antibody resensitized tumors to sunitinib treatment. Sunitinib 181-190 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 20103651-7 2010 In patients who were refractory to sunitinib treatment, IL-8 expression was elevated in ccRCC tumors, supporting the concept that IL-8 levels might predict clinical response to sunitinib. Sunitinib 177-186 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 20103651-7 2010 In patients who were refractory to sunitinib treatment, IL-8 expression was elevated in ccRCC tumors, supporting the concept that IL-8 levels might predict clinical response to sunitinib. Sunitinib 177-186 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 20103651-8 2010 Our results reveal IL-8 as an important contributor to sunitinib resistance in ccRCC and a candidate therapeutic target to reverse acquired or intrinsic resistance to sunitinib in this malignancy. Sunitinib 55-64 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 20103651-8 2010 Our results reveal IL-8 as an important contributor to sunitinib resistance in ccRCC and a candidate therapeutic target to reverse acquired or intrinsic resistance to sunitinib in this malignancy. Sunitinib 167-176 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 19889021-9 2010 CBMC activation with the PAR-2 activating peptide resulted in an increased secretion of IL-8, but no histamine release was observed. cbmc 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 19884117-7 2010 From receptor binding analysis AAL-glycan was found to bind IL-8 receptors especially CXCR2 directly and such binding could be blocked by 3"- or 2"-fucosyllactose. 3"- or 2"-fucosyllactose 138-162 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 20005571-7 2010 By contrast, STBM washed from the maternal side of a placental cotyledon and STBM shed by explants cultured in air up-regulated cell surface expression of the adhesion molecule CD54 and induced the production of interleukin (IL)-8, IL-6 and IL-1beta. stbm 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 212-230 20065153-11 2010 RT-PCR showed a strong tumor necrosis factor alpha mRNA increase with IL-8 that was blocked by aldosterone, excluding the possibility that the tumor necrosis factor alpha increase was merely a consequence of secretion. Aldosterone 95-106 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 20007751-5 2010 Cholecalciferol therapy reduced circulating levels of inflammatory cytokines, including IL-8, IL-6, and TNF. Cholecalciferol 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 19648651-3 2010 This study investigates the effect of the lipid-rich surfactant preparations Survanta, Curosurf, and the major surfactant phospholipid dipalmitoylphosphatidylcholine (DPPC) on interleukin-8 (IL-8) gene and protein expression in human A549 lung epithelial cells using immunoassay and PCR techniques. phospholipid dipalmitoylphosphatidylcholine 122-165 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 19648651-3 2010 This study investigates the effect of the lipid-rich surfactant preparations Survanta, Curosurf, and the major surfactant phospholipid dipalmitoylphosphatidylcholine (DPPC) on interleukin-8 (IL-8) gene and protein expression in human A549 lung epithelial cells using immunoassay and PCR techniques. phospholipid dipalmitoylphosphatidylcholine 122-165 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 19648651-3 2010 This study investigates the effect of the lipid-rich surfactant preparations Survanta, Curosurf, and the major surfactant phospholipid dipalmitoylphosphatidylcholine (DPPC) on interleukin-8 (IL-8) gene and protein expression in human A549 lung epithelial cells using immunoassay and PCR techniques. 1,2-Dipalmitoylphosphatidylcholine 167-171 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 19648651-5 2010 The lipid-rich surfactant preparations Survanta, Curosurf, and DPPC, at physiological concentrations, significantly downregulated lipopolysaccharide (LPS)-induced IL-8 expression in A549 cells both at the mRNA and protein levels. 1,2-Dipalmitoylphosphatidylcholine 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 20043079-0 2010 Xanthohumol, a prenylated chalcone derived from hops, inhibits proliferation, migration and interleukin-8 expression of hepatocellular carcinoma cells. xanthohumol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 20026745-2 2010 Inflammation is mediated by inflammatory cytokines, including IL-8, which illustrates an increase in biological half-life and proinflammatory activity when bound to glycosaminoglycans (GAGs). Glycosaminoglycans 165-183 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 20026745-3 2010 The aim of this project was to compare IL-8 and IL-18 for their relative stability, activity, and interaction with GAGs, including chondroitin sulfate, hyaluronic acid, and heparan sulfate, present in high quantities in the lungs of patients with CF. Chondroitin Sulfates 131-150 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 20026745-3 2010 The aim of this project was to compare IL-8 and IL-18 for their relative stability, activity, and interaction with GAGs, including chondroitin sulfate, hyaluronic acid, and heparan sulfate, present in high quantities in the lungs of patients with CF. Hyaluronic Acid 152-167 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 20026745-3 2010 The aim of this project was to compare IL-8 and IL-18 for their relative stability, activity, and interaction with GAGs, including chondroitin sulfate, hyaluronic acid, and heparan sulfate, present in high quantities in the lungs of patients with CF. Heparitin Sulfate 173-188 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 20004976-4 2010 The agent displayed enhanced binding to GAG structures in vitro and could antagonize CXCL8-induced firm adhesion of monocytes as well as neutrophils to activated microvascular endothelium in physiologic flow assays. Glycosaminoglycans 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 85-90 20005571-7 2010 By contrast, STBM washed from the maternal side of a placental cotyledon and STBM shed by explants cultured in air up-regulated cell surface expression of the adhesion molecule CD54 and induced the production of interleukin (IL)-8, IL-6 and IL-1beta. stbm 77-81 C-X-C motif chemokine ligand 8 Homo sapiens 212-230 19722605-4 2010 The sol-gel matrices were produced via the NaF-catalyzed hydrolysis of a mixture of tetramethyoxysilane (TMOS) and methyltrimethoxysilane (MTMS), yielding nanohybrid matrices with controlled pore sizes, pore volumes, and surface chemistry. tetramethyoxysilane 84-103 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 20022380-8 2010 Interestingly, IL-8 and ICAM-1 had a modest effect on neutrophil TEM in this 3h assay which was significantly diminished by the inhibition of Rho kinase in HUVECs with Y27632. Tritium 77-79 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 20022380-8 2010 Interestingly, IL-8 and ICAM-1 had a modest effect on neutrophil TEM in this 3h assay which was significantly diminished by the inhibition of Rho kinase in HUVECs with Y27632. Y 27632 168-174 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 19722605-4 2010 The sol-gel matrices were produced via the NaF-catalyzed hydrolysis of a mixture of tetramethyoxysilane (TMOS) and methyltrimethoxysilane (MTMS), yielding nanohybrid matrices with controlled pore sizes, pore volumes, and surface chemistry. tetramethoxysilane 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 19722605-4 2010 The sol-gel matrices were produced via the NaF-catalyzed hydrolysis of a mixture of tetramethyoxysilane (TMOS) and methyltrimethoxysilane (MTMS), yielding nanohybrid matrices with controlled pore sizes, pore volumes, and surface chemistry. methyltrimethoxysilane 115-137 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 19722605-4 2010 The sol-gel matrices were produced via the NaF-catalyzed hydrolysis of a mixture of tetramethyoxysilane (TMOS) and methyltrimethoxysilane (MTMS), yielding nanohybrid matrices with controlled pore sizes, pore volumes, and surface chemistry. methyltrimethoxysilane 139-143 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 20098709-10 2010 The effects of the concentration of morphine found in serum of septic patients on LPS-induced release of IL-8 by human neutrophils were tested. Morphine 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 20098709-13 2010 LPS and IL-8 were able to induce a significant release of morphine only in presence of Ca(2+). Morphine 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 20439185-0 2010 Vitamin D derivatives: calcitriol and tacalcitol inhibits interleukin-6 and interleukin-8 expression in human nasal polyp fibroblast cultures. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 20098709-15 2010 Low concentration of morphine (8 nM) significantly inhibited the release of IL-8 from neutrophils when coincubated with LPS. Morphine 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 20098709-20 2010 Morphine concentrations equivalent to those found in the serum of septic patients significantly inhibited LPS-induced IL-8 secretion in neutrophils. Morphine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 19799982-1 2010 AIM OF THE STUDY: In order to elucidate immunoregulatory mechanisms of Cordyceps militaris, a methanol extract of Cordyceps militaris grown on germinated soybeans was prepared and its immunoregulatory effect in the human lung epithelial cells was investigated by examining its ability to induce IL-8 expression. Methanol 94-102 C-X-C motif chemokine ligand 8 Homo sapiens 295-299 19949019-8 2010 For example, increases in IL-8 with VCP, MMP-9 with CP, and VEGF with vandetanib monotherapy were associated with increased progression risk, and increase in intercellular adhesion molecule 1 with vandetanib was associated with decreased risk. vandetanib 70-80 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20439185-0 2010 Vitamin D derivatives: calcitriol and tacalcitol inhibits interleukin-6 and interleukin-8 expression in human nasal polyp fibroblast cultures. 1 alpha,24-dihydroxyvitamin D3 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 20439185-3 2010 The purpose of this study was to investigate the influence of 1alpha,25-dihydroxyvitamin D3 (calcitriol) and 1alpha,24(R)-dihydroxyvitamin D3 (tacalcitol) on the secretion of IL-6 and IL-8 by fibroblasts derived from NP. Calcitriol 62-91 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 20439185-3 2010 The purpose of this study was to investigate the influence of 1alpha,25-dihydroxyvitamin D3 (calcitriol) and 1alpha,24(R)-dihydroxyvitamin D3 (tacalcitol) on the secretion of IL-6 and IL-8 by fibroblasts derived from NP. 1 alpha,24-dihydroxyvitamin D3 109-141 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 20439185-8 2010 RESULTS: Treatment with calcitriol or tacalcitol inhibits the synthesis of both IL-6 and IL-8 compared to the control group. Calcitriol 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 20439185-8 2010 RESULTS: Treatment with calcitriol or tacalcitol inhibits the synthesis of both IL-6 and IL-8 compared to the control group. 1 alpha,24-dihydroxyvitamin D3 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 20439185-12 2010 CONCLUSIONS: The present study demonstrates that calcitriol and tacalcitol are capable of affecting pro-inflammatory cytokine (IL-6 and IL-8) levels in NP cultures. Calcitriol 49-59 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 20439185-12 2010 CONCLUSIONS: The present study demonstrates that calcitriol and tacalcitol are capable of affecting pro-inflammatory cytokine (IL-6 and IL-8) levels in NP cultures. 1 alpha,24-dihydroxyvitamin D3 64-74 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 20439185-0 2010 Vitamin D derivatives: calcitriol and tacalcitol inhibits interleukin-6 and interleukin-8 expression in human nasal polyp fibroblast cultures. Calcitriol 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 19595352-0 2010 Lovastatin inhibits oxidized L-A-phosphatidylcholine B-arachidonoyl-gamma-palmitoyl (ox-PAPC)-stimulated interleukin-8 mRNA and protein synthesis in human aortic endothelial cells by depleting stores of geranylgeranyl pyrophosphate. Lovastatin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 19346317-0 2010 Cell-bound IL-8 increases in bronchial epithelial cells after arylsulfatase B silencing due to sequestration with chondroitin-4-sulfate. Chondroitin Sulfates 114-135 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19346317-2 2010 To determine the role of chondroitin-4-sulfate (C4S) in mediating effects of IL-8, we silenced the enzyme N-acetylgalactosamine-4-sulfatase (arylsulfatase B [ASB]) that removes the 4-sulfate group from C4S, in the IB3-1 and C38 bronchial epithelial cell lines and in normal primary bronchial epithelial cells. Chondroitin Sulfates 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 19834107-0 2010 Adenosine modulates HIF-1{alpha}, VEGF, IL-8, and foam cell formation in a human model of hypoxic foam cells. Adenosine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 19346317-3 2010 When ASB was silenced and IL-8 production stimulated by exposure to TNF-alpha, ASB activity declined by roughly 75%, cellular C4S content increased by over 7.5 microg/mg protein, cell-bound IL-8 increased by over 530 pg/mg protein, and secreted IL-8 declined by over 520 pg/mg protein in all cell lines (P < 0.001). Chondroitin Sulfates 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 19346317-8 2010 These findings provide evidence for the influential role of ASB and C4S in the regulation of IL-8 secretion, and suggest that changes in ASB activity and C4S content may have a significant impact on IL-8-mediated inflammatory responses. Chondroitin Sulfates 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 19346317-8 2010 These findings provide evidence for the influential role of ASB and C4S in the regulation of IL-8 secretion, and suggest that changes in ASB activity and C4S content may have a significant impact on IL-8-mediated inflammatory responses. Chondroitin Sulfates 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 20113495-8 2010 RESULTS: After TNFalpha stimulation, the mRNA expression level of some of the genes under NF-kappaB control, such as interleukin (IL)-6 and IL-8, increased, while treatment with GlcN and NAPA reverted the effect. Glucosamine 178-182 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 20113495-8 2010 RESULTS: After TNFalpha stimulation, the mRNA expression level of some of the genes under NF-kappaB control, such as interleukin (IL)-6 and IL-8, increased, while treatment with GlcN and NAPA reverted the effect. Acecainide 187-191 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 19595352-0 2010 Lovastatin inhibits oxidized L-A-phosphatidylcholine B-arachidonoyl-gamma-palmitoyl (ox-PAPC)-stimulated interleukin-8 mRNA and protein synthesis in human aortic endothelial cells by depleting stores of geranylgeranyl pyrophosphate. l-a-phosphatidylcholine b-arachidonoyl-gamma-palmitoyl 29-83 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 19595352-1 2010 Human aortic endothelial cells (HAEC) exposed to 50 microg/ml oxidized L-A-phosphatidylcholine B-arachidonoyl-gamma-palmitoyl (ox-PAPC) for 6h increased in interleukin-8 mRNA and protein levels. l-a-phosphatidylcholine b-arachidonoyl-gamma-palmitoyl 71-125 C-X-C motif chemokine ligand 8 Homo sapiens 156-169 19595352-4 2010 Addition of the geranylgeraniol (GGOL, 10 microM) but not farnesol (FOL, 10 microM), reversed the inhibitory effect of lovastatin on interleukin-8 mRNA and protein levels stimulated by ox-PAPC, indicating that lovastatin exerted its effect by inhibiting stores of geranylgeranyl pyrophosphate (GGPP) which are necessary for geranylgeranylation of proteins. geranylgeraniol 16-31 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 19595352-4 2010 Addition of the geranylgeraniol (GGOL, 10 microM) but not farnesol (FOL, 10 microM), reversed the inhibitory effect of lovastatin on interleukin-8 mRNA and protein levels stimulated by ox-PAPC, indicating that lovastatin exerted its effect by inhibiting stores of geranylgeranyl pyrophosphate (GGPP) which are necessary for geranylgeranylation of proteins. geranylgeraniol 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 19595352-4 2010 Addition of the geranylgeraniol (GGOL, 10 microM) but not farnesol (FOL, 10 microM), reversed the inhibitory effect of lovastatin on interleukin-8 mRNA and protein levels stimulated by ox-PAPC, indicating that lovastatin exerted its effect by inhibiting stores of geranylgeranyl pyrophosphate (GGPP) which are necessary for geranylgeranylation of proteins. Lovastatin 119-129 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 20699615-12 2010 Surface fluoride concentration was significantly increased by native TiF(4), native and buffered AmF, buffered ZnF(2), and buffered NaF application. Fluorides 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 132-135 21526274-7 2010 Interleukin-8 secretion was significantly reduced after 24h incubation with the NO* donor, sodium nitroprusside. Nitroprusside 91-111 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 21526274-10 2010 Inhibition of endogenous NO* with the nitric oxide synthase inhibitor N-nitro-L-arginine-methyl-ester caused an increase in IL-8 secretion by lipopolysaccharide- and cytokine-stimulated BEAS-2B cells. nitric 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 21526274-10 2010 Inhibition of endogenous NO* with the nitric oxide synthase inhibitor N-nitro-L-arginine-methyl-ester caused an increase in IL-8 secretion by lipopolysaccharide- and cytokine-stimulated BEAS-2B cells. n-nitro-l-arginine-methyl-ester 70-101 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 20332635-6 2010 In addition, DHMEQ induces a significant dose-dependent decrease in ICAM expression, MCP-1, RANTES, and IL-8 release. dehydroxymethylepoxyquinomicin 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 19783455-6 2010 RESULTS: Dexamethasone inhibited LPS-stimulated release of TauNuFalpha, of IL-6, of IL-8 and of IL-10 in dose-dependent manner. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 21063104-9 2010 In contrast, endothelial cells showed higher IL-6 and IL-8 release under co-culture conditions than in monolayers, with IL-8 production being largely suppressed by L-NMMA but not by 4-ABH(4). N(G)-monomethylarginine acetate 164-170 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 20374186-7 2010 Cultures of human mononuclear leukocytes collected from six healthy volunteers showed 100 nM of azelnidipine caused significant inhibition of formyl-methyonyl leucyl phenylalanine (fMLP)-induced production of IL-8. azelnidipine 96-108 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 20374186-7 2010 Cultures of human mononuclear leukocytes collected from six healthy volunteers showed 100 nM of azelnidipine caused significant inhibition of formyl-methyonyl leucyl phenylalanine (fMLP)-induced production of IL-8. formyl-methyonyl leucyl phenylalanine 142-179 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 20472994-3 2010 In our previous study, it was found that PMMA-CHDF could efficiently remove various pro-inflammatory cytokines such as TNFalpha, IL-6 and IL-8 from the bloodstream, resulting in early recovery from septic shock. pmma-chdf 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 20472995-7 2010 Significant correlations between changes in blood levels of cytokines (IL-6 and IL-8) and changes in RI were demonstrated in the PMMA-CHDF group. Polymethyl Methacrylate 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 20472995-7 2010 Significant correlations between changes in blood levels of cytokines (IL-6 and IL-8) and changes in RI were demonstrated in the PMMA-CHDF group. chdf 134-138 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 19165599-6 2010 Ethanol, but not acetaldehyde or PAEE, induced interleukin-8 production. Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 19906815-0 2010 Lysophosphatidic acid up-regulates expression of growth-regulated oncogene-alpha, interleukin-8, and monocyte chemoattractant protein-1 in human first-trimester trophoblasts: possible roles in angiogenesis and immune regulation. lysophosphatidic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 19906815-12 2010 LPA-induced IL-8 protein secretion of trophoblasts enhanced permeability, migration, proliferation, and capillary tube formation of human endometrial microvascular endothelial cells. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 19789931-7 2010 Moreover, AAS significantly inhibited production of inflammatory cytokines, tumor necrosis factor (TNF), interleukin (IL)-6, and IL-8 on the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated human mast cell line, HMC-1 cells. Tetradecanoylphorbol Acetate 141-172 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 19222504-7 2010 Grafts with hepatic IL-8 release exhibited subsequently higher alkaline phosphatase [319 (213-405) IU/L vs. 175 (149-208) IU/L, p = 0.006] and bilirubin [101 (44-139) micromol/L vs. 30 (23-72) micromol/L, p = 0.029] levels after transplantation. Bilirubin 143-152 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 19789931-7 2010 Moreover, AAS significantly inhibited production of inflammatory cytokines, tumor necrosis factor (TNF), interleukin (IL)-6, and IL-8 on the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated human mast cell line, HMC-1 cells. Calcium 177-184 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 19250704-3 2010 In this study we investigated the production of the pro-inflammatory cytokines tumour necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta) and interleukin-8 (CXCL8) in these three cell types upon stimulation with lipoteichoic acid (LTA), a cell wall component of Gram-positive bacteria that activates the pattern recognition molecule Toll-like receptor 2 (TLR2). lipoteichoic acid 224-241 C-X-C motif chemokine ligand 8 Homo sapiens 169-174 19752565-10 2010 Stimulation with poly(I:C) increased the percentage of CD11b+ cells and enhanced the secretion of IL-8, effects mediated via the p38 mitogen-activated protein kinases and nuclear factor-kappaB signaling pathways. Poly I-C 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 19250704-3 2010 In this study we investigated the production of the pro-inflammatory cytokines tumour necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta) and interleukin-8 (CXCL8) in these three cell types upon stimulation with lipoteichoic acid (LTA), a cell wall component of Gram-positive bacteria that activates the pattern recognition molecule Toll-like receptor 2 (TLR2). lipoteichoic acid 243-246 C-X-C motif chemokine ligand 8 Homo sapiens 169-174 19818417-9 2010 qPCR and ELISA showed that IL-8 levels were increased by CSE, with suppression by dexamethasone. Dexamethasone 82-95 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 19752565-11 2010 Moreover, pretreatment with IL-5 augmented the poly(I:C)-induced IL-8 release. Poly I-C 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 20871847-10 2010 In the active vitamin D group, we found a significant median percent decline in levels of GM-CSF (-62.9%, P < .0001), IFN-gamma (-38.9%, P < .0001), IL-4 (-50.8%, P = .001), IL-8 (-48.4%, P < .0001), and IL-10 (-70.4%, P < .0001). Vitamin D 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 19672095-4 2010 METHODS: Rupatadine (1-50 microM) was used before stimulation by: (1) interleukin (IL)-1 to induce IL-6 from human leukemic mast cells (HMC-1 cells), (2) substance P for histamine, IL-8 and vascular endothelial growth factor release from LAD2 cells, and (3) IgE/anti-IgE for cytokine release from human cord blood-derived cultured mast cells. rupatadine 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 19672095-7 2010 Rupatadine (10-50 microM for 10 min) inhibited IL-8 (80%), vascular endothelial growth factor (73%) and histamine (88%) release from LAD2 cells, as well as IL-6, IL-8, IL-10, IL-13 and tumor necrosis factor release from human cord blood-derived cultured mast cells. rupatadine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 19672095-7 2010 Rupatadine (10-50 microM for 10 min) inhibited IL-8 (80%), vascular endothelial growth factor (73%) and histamine (88%) release from LAD2 cells, as well as IL-6, IL-8, IL-10, IL-13 and tumor necrosis factor release from human cord blood-derived cultured mast cells. rupatadine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 19779130-5 2010 Acid forms of the nicotinamide glycolate were inactive in whole-cell assays of chemotaxis and calcium flux, but they inhibited (125)I-CXCL8/CXCR2 binding and CXCL1-stimulated [(35)S]GTPgammaS exchange. nicotinamide glycolate 18-40 C-X-C motif chemokine ligand 8 Homo sapiens 134-139 20936184-0 2010 Induction by TNF-alpha of IL-6 and IL-8 in cystic fibrosis bronchial IB3-1 epithelial cells encapsulated in alginate microbeads. Alginates 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 19880789-10 2010 Furthermore, cortisone decreased IL-6 (P < 0.005), IL-8 (P < 0.05), and macrophage chemoattractant protein-1 (P < 0.05) production by cultured TAO cells only, an effect that was abrogated by inhibition of 11beta-HSD1. Cortisone 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 19779130-3 2010 The data presented here describe the cellular pharmacology of the acid and ester forms of the nicotinamide glycolate pharmacophore, a potent antagonist of CXCR2 signaling by the chemokines CXCL1 and CXCL8. Esters 75-80 C-X-C motif chemokine ligand 8 Homo sapiens 199-204 20634942-5 2010 The expression of CD11b/CD18 on neutrophils and E-selectin/ICAM-1 on HUVECs, and the adherence between neutrophils and HUVECs were significantly increased in 10 SP/MEC-CM, and the increments were significantly blocked by anti-IL-8 antibody. mec 164-167 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 19779130-3 2010 The data presented here describe the cellular pharmacology of the acid and ester forms of the nicotinamide glycolate pharmacophore, a potent antagonist of CXCR2 signaling by the chemokines CXCL1 and CXCL8. nicotinamide glycolate 94-116 C-X-C motif chemokine ligand 8 Homo sapiens 199-204 19779130-4 2010 Ester forms of the nicotinamide glycolate antagonized CXCL1-stimulated chemotaxis (IC(50) = 42 nM) and calcium flux (IC(50) = 48 nM) in human neutrophils, but they were inactive in cell-free assays of (125)I-CXCL8/CXCR2 binding and CXCL1-stimulated guanosine 5"-O-(3-[(35)S]thio)triphosphate ([(35)S]GTPgammaS) exchange. Esters 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 208-213 19779130-4 2010 Ester forms of the nicotinamide glycolate antagonized CXCL1-stimulated chemotaxis (IC(50) = 42 nM) and calcium flux (IC(50) = 48 nM) in human neutrophils, but they were inactive in cell-free assays of (125)I-CXCL8/CXCR2 binding and CXCL1-stimulated guanosine 5"-O-(3-[(35)S]thio)triphosphate ([(35)S]GTPgammaS) exchange. nicotinamide glycolate 19-41 C-X-C motif chemokine ligand 8 Homo sapiens 208-213 21253500-7 2010 ELISA showed that KBG and paeoniflorin suppressed the production of MIF, IL-6, IL-8, and TNF-alpha in LPS-stimulated HDMECs. peoniflorin 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 20634942-6 2010 CONCLUSION: MEC and IL-8 are major factors for neutrophil recruitment in nonallergic CRS. Chromium 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 21103619-7 2010 RESULTS: The IL-2 production of T-lymphocytes was a deficient one (low seric levels in the majority of the patients), while cytokines IL-6, IL-8 and TNF-alpha showed high seric levels. seric 171-176 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 20480060-0 2010 Release of fluoride from fresh and old NaF-impregnated chewing sticks (Miswaks) in vitro and oral retention in vivo. Fluorides 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 20480060-1 2010 PURPOSE: The objectives of the present investigation were to study fluoride (F) release from NaF-impregnated chewing sticks (Miswaks) in vitro and to study the F clearance in saliva and the F oral retention in vivo. Fluorides 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 20360623-0 2010 N-acetylcysteine inhibits IL-8 and MMP-9 release and ICAM-1 expression by bronchoalveolar cells from interstitial lung disease patients. Acetylcysteine 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20360623-7 2010 NAC exerted a dose-dependent inhibitory effect on IL-8 and MMP-9 release and ICAM- expression by BAL macrophages and lymphocytes from patients with IPF and sarcoidosis. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 20703999-8 2010 In contrast, IL-8 concentration in EBC (pg/ml) decreased after FOB (0.073 +/- 0.13 v. 0.061 +/- 0.1, p = 0.006) and was significantly lower than in BALF (BALF 0.95 +/- 0.62, p < 0.05). NSC638702 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19816000-3 2010 OBJECTIVES: The aim of the study was to determine whether the pH , electrical conductivity and the levels of ammonium and interleukin 8 (IL-8) of EBC were altered in smokers and whether they changed after smoking a single cigarette. NSC638702 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 122-135 19816000-3 2010 OBJECTIVES: The aim of the study was to determine whether the pH , electrical conductivity and the levels of ammonium and interleukin 8 (IL-8) of EBC were altered in smokers and whether they changed after smoking a single cigarette. NSC638702 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 19887769-2 2010 OBJECTIVE: To test the hypothesis that clinically relevant concentrations of ibuprofen suppress activation of nuclear factor (NF)-kappaB and thus down-regulate stimulated interleukin (IL)-8 production in CF respiratory epithelial cells. Ibuprofen 77-86 C-X-C motif chemokine ligand 8 Homo sapiens 171-189 19887769-6 2010 NF-kappaB and IL-8 suppression by ibuprofen (480 microM) was compared to dexamethasone (5 nM). Ibuprofen 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 19887769-10 2010 By contrast, dexamethasone significantly down-regulated stimulated IL-8 mRNA and protein. Dexamethasone 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 19887769-13 2010 We speculate that NF-kappaB-independent mechanisms may be responsible for anti-IL-8 effects of dexamethasone. Dexamethasone 95-108 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 20615159-9 2010 IL-6, TNF, and IL-8 were higher in patients vs. controls before treatment (p < 0.05&#x2013;0.001), and decreased after treatment in patients (p < 0.001) but did not change in controls. Adenosine Monophosphate 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 20090409-4 2010 Quantitative PCR analysis was used to detect gene expression changes, particularly of interleukin (IL) 8, as an indicator of differential dendritic cell (DC) gene expression after sensitizer stimulation in the absence or presence of tacrolimus and betamethasone at two different concentrations. Betamethasone 248-261 C-X-C motif chemokine ligand 8 Homo sapiens 86-104 20238282-6 2010 The fluoride uptake was slightly higher when the enamel samples were brushed with NaF toothpaste, rather than just stored in the respective toothpaste slurry. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 20090409-6 2010 Betamethasone and, to a lesser extent, tacrolimus led to a marked reduction of chemical-induced IL-8 expression by TNBS and CAld. Betamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 20090409-6 2010 Betamethasone and, to a lesser extent, tacrolimus led to a marked reduction of chemical-induced IL-8 expression by TNBS and CAld. Tacrolimus 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 20090409-6 2010 Betamethasone and, to a lesser extent, tacrolimus led to a marked reduction of chemical-induced IL-8 expression by TNBS and CAld. Trinitrobenzenesulfonic Acid 115-119 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 21341456-6 2010 CONCLUSION: The elevated levels of IL-6, IL-16, alpha-TNF, and the chemokine IL-8 with the lower blood content of the cytokine IL-4 were long before the development of DM1 in children with normal blood glucose level in the presence of LIAA, which should be borne in mind while developing the immune mechanisms specifically directed against block, which participate by means of cytokines in beta-cell destruction, as well as methods for preventing the development of T1DM in subjects with LIAA. Glucose 202-209 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 20025541-10 2010 CONCLUSION: We have demonstrated that iodide stimulates thyroid follicular cells to produce chemokines, particularly CCL2, CXCL8, and CXCL14. Iodides 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 20056081-0 2010 [Relationship of IL-6 and IL-8 secretion in epithelial ovarian cancer cell lines with their sensitivity to tamoxifen as well as MAPK, Akt and estrogen receptor phosphorylation]. Tamoxifen 107-116 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20002897-9 2010 DEX dose dependently down-regulated basal and MMC-induced interleukin-8 and monocyte chemoattractant protein-1 mRNA expression and protein secretion. Dexamethasone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 20002897-11 2010 These suggested that DEX may inhibit MMC-induced interleukin-8 and monocyte chemoattractant protein-1 by up-regulating MKP-1 expression, which subsequently deactivated p38 and Jun N-terminal kinases activation. Dexamethasone 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 20002897-11 2010 These suggested that DEX may inhibit MMC-induced interleukin-8 and monocyte chemoattractant protein-1 by up-regulating MKP-1 expression, which subsequently deactivated p38 and Jun N-terminal kinases activation. Mitomycin 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 20056081-1 2010 AIM: To investigate the relationship of IL-6 and IL-8 secretion in four epithelial ovarian cancer cell lines (A2780, CAOV-3, SKOV-3 and ES-2) with their sensitivity to tamoxifen (TAM) as well as MAPK, Akt and estrogen receptor (ER) phosphorylation, and to explore the mechanism of endocrine therapy resistance caused by IL-6 and IL-8 in ovarian cancer cells. Tamoxifen 168-177 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 20056081-10 2010 CONCLUSION: Autocrine production of IL-6 and IL-8 in epithelial ovarian cancer cell lines is inversely associated with cell response to TAM, and positively associated with phosphorylated MAPK, Akt and ER. Tamoxifen 136-139 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 19951001-8 2009 Sesamin also attenuated the oxLDL-induced activation of NF-kappaB, suggesting that the inhibitory effects of sesamin on IL-8 and ET-1 release, adhesion molecule expression, and the adherence of THP-1 cells were at least partially through the blockade of NF-kappaB activation. sesamin 109-116 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 19880520-4 2009 Hypoxia enhanced interleukin-1beta-induced interleukin-8 (CXCL8) production in A549 cells and decreased the ability of dexamethasone to suppress the CXCL8 production. Dexamethasone 119-132 C-X-C motif chemokine ligand 8 Homo sapiens 149-154 19688831-6 2009 Plasma IL-8 correlated strongly to plasma citrulline (n = 46, rho = -0.627; P < 0.001). Citrulline 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 19836502-3 2009 Running buffer containing 40 mmol/L 1-butyl-3-methylimidazolium tetrafluoroborate (BMImBF(4)) IL-8 mmol/L phosphate resulted in significant changes in separation selectivity for alkaloids with similar structures. 1-butyl-3-methylimidazolium tetrafluoroborate 36-81 C-X-C motif chemokine ligand 8 Homo sapiens 83-98 19836502-3 2009 Running buffer containing 40 mmol/L 1-butyl-3-methylimidazolium tetrafluoroborate (BMImBF(4)) IL-8 mmol/L phosphate resulted in significant changes in separation selectivity for alkaloids with similar structures. Phosphates 106-115 C-X-C motif chemokine ligand 8 Homo sapiens 83-98 19836502-3 2009 Running buffer containing 40 mmol/L 1-butyl-3-methylimidazolium tetrafluoroborate (BMImBF(4)) IL-8 mmol/L phosphate resulted in significant changes in separation selectivity for alkaloids with similar structures. Alkaloids 178-187 C-X-C motif chemokine ligand 8 Homo sapiens 83-98 19968887-7 2009 With regard to extravasation we found norepinephrine to induce adhesion of activated CD8+ T cells: norepinephrine increased the interleukin-8 release from endothelium, which in turn had effect on the activated CXCR1+ CD8+ T cells. Norepinephrine 38-52 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 19968887-7 2009 With regard to extravasation we found norepinephrine to induce adhesion of activated CD8+ T cells: norepinephrine increased the interleukin-8 release from endothelium, which in turn had effect on the activated CXCR1+ CD8+ T cells. Norepinephrine 99-113 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 20015351-8 2009 Dose-response measurements with ZnO nanoparticles (0.3-8.5 mug/cm(2)) showed significant differences in mRNA expression of pro-inflammatory (IL-8) and oxidative stress (HO-1) markers when comparing submerged and air-liquid interface exposures. Zinc Oxide 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 20016852-10 2009 In addition, polymorphism CXCR1_G827C was associated with increased CXCL-8 levels in women with ASB (P = 0.004). asb 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 68-74 20003431-4 2009 RESULTS: Congaplex enhanced phytohemagglutinin/phorbol 12-myristate 13-acetate (PHA/PMA) stimulation of both CEM and Jurkat cells as measured by the production of cytokines, while Immuplex suppressed PHA/PMA-induced production of cytokines, with the exception of interleukin (IL)-8 which was enhanced by Immuplex. congaplex 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 263-281 19826413-8 2009 In MyD88(+) SCOV3 cells, LPS or PTX binding to TLR4 induced IRAK4 activation and cJun phosphorylation, activated the NF-kappaB pathway and promoted interleukin (IL)-8, IL-6, vascular endothelial growth factor and monocyte chemotactic protein-1 production and resistance to drug-induced apoptosis. Paclitaxel 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 148-166 19265173-8 2009 Application of alpha,beta-meATP or BzATP at the apical side of polarized human primary nasal epithelial cells sufficed to cause CaMK-dependent IL-8 release by these cells. BzATP 35-40 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 19779021-5 2009 Using the cytokine IL-8 as a physiological read out of the inflammatory response, we found that TLR3 is the most functional of the expressed TLRs in both primary and immortalized esophageal epithelial cell lines in response to its synthetic ligand polyinosinic polycytidylic acid [poly(I:C)]. Poly I-C 248-279 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 19779021-6 2009 Through reporter gene studies, we show that poly(I:C)-induced NF-kappaB activation is critical for the transactivation of the IL-8 promoter in vitro and that nuclear translocation of NF-kappaB occurs at an early time point following poly(I:C) stimulation of esophageal epithelial cells. Poly I-C 44-53 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 19779021-6 2009 Through reporter gene studies, we show that poly(I:C)-induced NF-kappaB activation is critical for the transactivation of the IL-8 promoter in vitro and that nuclear translocation of NF-kappaB occurs at an early time point following poly(I:C) stimulation of esophageal epithelial cells. Poly I-C 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 19265173-2 2009 The aim of our study was to investigate the molecular mechanisms involved in the ATP-dependent regulation of IL-8 production by airway epithelial cells. alpha,beta-methyleneadenosine 5'-triphosphate 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 19265173-6 2009 Both alpha,beta-meATP and BzATP caused Ca(2+)-dependent binding of phosphorylated p65 (S536) NF-kappaB subunit to the endogenous IL-8 gene promoter in NT-1 cells. BzATP 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 19265173-9 2009 Thus, ATP promotes TNF-alpha-elicited IL-8 expression through P2X ion channel-triggered Ca(2+) entry, leading to CaMK-dependent IKK activation and binding of active p65 to IL-8 gene promoter. alpha,beta-methyleneadenosine 5'-triphosphate 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 19265173-9 2009 Thus, ATP promotes TNF-alpha-elicited IL-8 expression through P2X ion channel-triggered Ca(2+) entry, leading to CaMK-dependent IKK activation and binding of active p65 to IL-8 gene promoter. alpha,beta-methyleneadenosine 5'-triphosphate 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 19799602-9 2009 The main mechanism of E(2) protection in NaF exposure appeared to be connected with the influence of E(2 )on thiol group levels, not (*)OH scavenging ability. Estradiol 101-106 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 20112520-1 2009 OBJECTIVES: We assessed the effect of using preoperative sodium fluoride (NaF) on the difficulty of working with the footplate during stapedectomy and its effect on the postsurgical hearing gain in patients with mixed otosclerosis (i.e., otosclerosis and/or otospongiosis). Sodium Fluoride 57-72 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 19799602-9 2009 The main mechanism of E(2) protection in NaF exposure appeared to be connected with the influence of E(2 )on thiol group levels, not (*)OH scavenging ability. Sulfhydryl Compounds 109-114 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 20050188-10 2009 BK-induced IL-8 release was attenuated by inhibitors of phospholipase C (U73122), p38 (SB203580), JNK (SP600125), ERK 1/2 (PD98059) MAPKs, phosphoinositide 3-kinase (LY294002), NF-kappaB (BAY-117085) and by the glucocorticoid dexamethasone. SB 203580 87-95 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 20050188-10 2009 BK-induced IL-8 release was attenuated by inhibitors of phospholipase C (U73122), p38 (SB203580), JNK (SP600125), ERK 1/2 (PD98059) MAPKs, phosphoinositide 3-kinase (LY294002), NF-kappaB (BAY-117085) and by the glucocorticoid dexamethasone. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 166-174 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 20050188-10 2009 BK-induced IL-8 release was attenuated by inhibitors of phospholipase C (U73122), p38 (SB203580), JNK (SP600125), ERK 1/2 (PD98059) MAPKs, phosphoinositide 3-kinase (LY294002), NF-kappaB (BAY-117085) and by the glucocorticoid dexamethasone. Dexamethasone 226-239 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19917067-11 2009 While SLIGKV-induced IL-8 formation was reduced by both SB203580 and YM-254890, the response to K-14585 was sensitive to SB203580 but not YM-254890. SB 203580 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 19917067-11 2009 While SLIGKV-induced IL-8 formation was reduced by both SB203580 and YM-254890, the response to K-14585 was sensitive to SB203580 but not YM-254890. YM-254890 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 19773182-8 2009 CONCLUSIONS: In adolescents with T1DM and chronic, poor glucose control, increased serum IL-8 is associated with reduced IGF-1 suggesting a pro-inflammatory milieu that may contribute to alterations in the GH/IGF-1 axis. Glucose 56-63 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 19863450-8 2009 The IL-8 level was lower in tampons from women without vaginal S. aureus compared with women with S. aureus and was lower in study tampons with GML than in study tampons without GML. monolaurin 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 19863450-8 2009 The IL-8 level was lower in tampons from women without vaginal S. aureus compared with women with S. aureus and was lower in study tampons with GML than in study tampons without GML. monolaurin 178-181 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 19567495-9 2009 Desmosine levels were positively associated with plasma C-reactive protein (rho = 0.59; p = 0.03), sputum interleukin-8 (rho = 0.86; p < 0.01), and sputum neutrophil elastase (rho = 0.78; p < 0.01). Desmosine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 106-119 19863450-3 2009 The purpose of this study was to determine whether GML, as a tampon fiber finish, inhibits production of exotoxins and the cytokine interleukin 8 (IL-8) during normal tampon use. monolaurin 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 19683936-14 2009 CONCLUSION: Compared with simple cold blood cardioplegia in heart valve replacement patients, ADO pretreatment as an adjunct to 1 mmol l(-1) ADO cold blood cardioplegia may reduce cTnI, IL-6 and IL-8 release, resulting in reduced myocardial injury in ultrastructure after surgery. Adenosine 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 19643964-8 2009 The induced caspase-4 and caspase-3 activities by tunicamycin and the stimulated IL-8 protein expression by IL-1beta were markedly reduced by caspase-4 inhibitor Z-LEVD-fmk. Z-LEVD-FMK 162-172 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 19830732-4 2009 Butyrate was found to enhance PGN-mediated IL-8 and GRO-alpha production. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 19460789-6 2009 In these cells, methacholine also significantly augmented IL-8 secretion in combination with cigarette smoke extract in a synergistic manner, whereas synergistic effects on IL-6 secretion were not significant. Methacholine Chloride 16-28 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 19460789-7 2009 Muscarinic M3 receptors were the primary subtype involved in augmenting cigarette smoke extract-induced IL-8 secretion, as only tiotropium bromide and muscarinic M3 receptor subtype selective antagonists abrogated the effects of methacholine. Methacholine Chloride 229-241 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 19748599-0 2009 Serum levels of IL-8 and IL-6 in the long term pulmonary complications induced by sulfur mustard: Sardasht-Iran Cohort Study. Mustard Gas 82-96 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 19926600-11 2009 RBP 4 was positively correlated with IL-8 (r=0.416, P < 0.05) in human plasma in patients with DCMi. dcmi 98-102 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 19926600-14 2009 CONCLUSION: Elevated RBP 4 plasma concentrations, induced by IL-8, might be one mechanism leading to a higher incidence of diabetes in patients with DCMi. dcmi 149-153 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 20065508-0 2009 IL-6 and IL-8 responses of colorectal cancer in vivo and in vitro cancer cells subjected to simvastatin. Simvastatin 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 19602125-4 2009 MATERIAL AND METHODS: Differences in the expression of interleukin-1, interleukin-8 and RANKL mRNAs, in response to exposure to various concentrations of nicotine (0, 0.125, 0.25, 0.5 and 1 mm) were evaluated in U2OS cells using the reverse transcription-polymerase chain reaction.In addition, the levels of interleukin-1, interleukin-8 and RANKL proteins were determined using enzyme-linked immunosorbent assays. Nicotine 154-162 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 19602125-6 2009 RESULTS: Nicotine was found to increase the expression of interleukin-1, interleukin-8 and RANKL mRNA and protein in U2OS cells (p < 0.05). Nicotine 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 19897783-5 2009 In human gingival fibroblasts, cyclosporin alone did not induce evident inflammatory responses, but augmented the expression of CD54 and the production of interleukin (IL)-6 and IL-8 induced by TLR ligands, whereas phenytoin attenuated those responses. Cyclosporine 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 19915063-5 2009 We found that iloprost inhibited IFN-gamma- and IL-6-induced MCP-1, IL-8, RANTES, and TNF-alpha production in monocytes, indicating wide-ranging anti-inflammatory action. Iloprost 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 20065508-6 2009 Treatment of CRC with simvastatin (80 mg/day for 14 days) led to a significant decrease of serum IL-6, while the IL-8 level was less affected. Simvastatin 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 20388952-0 2009 Nitric oxide-induced IL-8 expression is mediated by NF-kappaB and AP-1 in gastric epithelial AGS cells. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 20065508-7 2009 The in vitro experiments on colorectal cancer-derived cell lines (HT-29 and Caco-2) demonstrated that application of simvastatin decreased generation of both IL-6 and IL-8. Simvastatin 117-128 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 20065508-9 2009 We conclude that 1) colorectal carcinogenesis is accompanied by increased synthesis and release of proinflammatory cytokines such as IL-6 and IL-8; 2) simvastatin therapy results in a decrease in serum level of proinflammatory cytokines, especially IL-6 in CRC and 3) simvastatin inhibits release of IL-8 and IL-6 from colorectal cell lines. Simvastatin 151-162 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 20065508-9 2009 We conclude that 1) colorectal carcinogenesis is accompanied by increased synthesis and release of proinflammatory cytokines such as IL-6 and IL-8; 2) simvastatin therapy results in a decrease in serum level of proinflammatory cytokines, especially IL-6 in CRC and 3) simvastatin inhibits release of IL-8 and IL-6 from colorectal cell lines. Simvastatin 151-162 C-X-C motif chemokine ligand 8 Homo sapiens 300-304 20046083-2 2009 Recent guidelines advocate two kinds of methods for sample collection and processing: either the sodium fluoride (NaF) method or immediate refrigeration using a serum separation tube (SST). Sodium Fluoride 97-112 C-X-C motif chemokine ligand 8 Homo sapiens 114-117 20046083-9 2009 NaF glucose showed a negative mean bias of 2.6 mg/dL vs SST glucose but showed high correlation (R=0.9899). Glucose 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 19811837-6 2009 As shown by neutrophils from an IRAK-4-deficient patient, the zymosan-induced IL-8 release was also independent of TLR2. Zymosan 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 19786303-3 2009 IL-8 expression was inhibited by nystatin (a lipid rafts inhibitor) but not by chlorpromazine (a clathrin-coated pits inhibitor). Nystatin 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19956406-6 2009 RESULTS: Incubation of HCFs with hydrocortisone markedly inhibited the expression of TLR2 and TLR4 mRNAs and decreased the release of IL-6 and IL-8 in a dose-dependent manner. Hydrocortisone 33-47 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 19810018-5 2009 Furthermore, naringin suppressed TNF-alpha-mediated release of interleukin-6 and -8 (IL-6 and IL-8). naringin 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 19583958-10 2009 SB202190 successfully suppressed IL-6, IL-8, PGE2, and PGF2alpha secretion in macrophage-exposed AF cells in response to TNF-alpha. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 19670249-9 2009 Transcription up-regulation of IL-6 and IL-8 was associated with re-expression of the serine active-site mutant prostasin in the PC-3 cells. Serine 86-92 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 19732821-5 2009 In response to 100 microM nickel sulphate MUTZ-3 DC revealed slightly upregulated mRNA levels after 24h, whereas 300 microM induced transcription of CCL3, CCL3L1 and IL8 significantly after 6 or 10h. nickel sulfate 26-41 C-X-C motif chemokine ligand 8 Homo sapiens 166-169 19801670-4 2009 In the present study, we assessed whether AMF promotes melanoma cell migration through autocrine production of IL-8. amf 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 20214329-7 2009 CONCLUSION: Injecting puerarin before CPB could effectively suppress the pro-inflammatory cytokines like TNF-alpha, IL-6 and IL-8; and enhance the expression of anti-inflammatory cytokines like IL-10, thus to alleviate the inflammatory reaction induced by CPB. puerarin 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 19956406-8 2009 The result of ELISA also showed the release of IL-6 and IL-8 can also be inhibited by hydrocortisone. Hydrocortisone 86-100 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 20214221-7 2009 Lovastatin administration resulted in the significant decrease of the pro-inflammatory cytokines IL-6 and TNF-alfa, while that of fluvastatin brought about the significant decrease of the serum levels of IL-6, IL-8 and TNF-alfa. Fluvastatin 130-141 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 19930544-11 2009 The concentrations of interleukin-8 were significantly correlated with increasing organic carbon concentrations. Carbon 90-96 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 19799411-5 2009 Sodium or lithium salts gave products, except with NaF, where silver fluoride in nitromethane was best for substitution by fluoride. silver fluoride 62-77 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 19799411-5 2009 Sodium or lithium salts gave products, except with NaF, where silver fluoride in nitromethane was best for substitution by fluoride. Fluorides 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 19809428-8 2009 AZ10397767 increased 17-AAG-induced apoptosis and necrosis and decreased NF-kappaB activity/CXCL8 expression in 17-AAG-treated PC3 cells. tanespimycin 112-118 C-X-C motif chemokine ligand 8 Homo sapiens 92-97 19750480-4 2009 Neutrophils pretreated with CXCL8, a chemokine that binds both CXCR1/2, completely blocked the calcium mobilization in response to LL-37, while LL-37 also partially inhibited (125)I-CXCL8 binding to neutrophils. Calcium 95-102 C-X-C motif chemokine ligand 8 Homo sapiens 28-33 19855073-9 2009 Taken together, the production of IL-8 by SPE B in A549 cells is mediated by Fas, and followed by the activation of FADD, caspase 8, MEKK1, ERK and NF-kappaB. ammonium ferrous sulfate 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 19446037-6 2009 Using proteosome inhibitor MG132 and I kappaB overexpression we demonstrated that an NF-kappaB-dependent mechanism was involved in both the activation of IL-8 and the repression of MCP-1 mRNA expression in response to hypoxia. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 19720161-0 2009 Modulation of expression of IL-8 gene in bronchial epithelial cells by 5-methoxypsoralen. 5-Methoxypsoralen 71-88 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 19787256-0 2009 Cepharanthine inhibits angiogenesis and tumorigenicity of human oral squamous cell carcinoma cells by suppressing expression of vascular endothelial growth factor and interleukin-8. cepharanthine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 19720161-7 2009 On the contrary, 5-methoxypsoralen resulted in IL-8 inhibition at 10 microM concentration, without effects on cell proliferation. 5-Methoxypsoralen 17-34 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 20067543-2 2009 Here we demonstrate that tumour-derived prostaglandin E2 (PGE(2)) and transforming growth factor-beta (TGF-beta) increase interleukin-8 (IL-8) but synergistically inhibit interferon-alpha (IFN-alpha) and tumour necrosis factor (TNF) production of Toll-like receptor 7 (TLR7)- and Toll-like receptor 9 (TLR9)-stimulated PDC. Dinoprostone 40-56 C-X-C motif chemokine ligand 8 Homo sapiens 122-135 20067543-2 2009 Here we demonstrate that tumour-derived prostaglandin E2 (PGE(2)) and transforming growth factor-beta (TGF-beta) increase interleukin-8 (IL-8) but synergistically inhibit interferon-alpha (IFN-alpha) and tumour necrosis factor (TNF) production of Toll-like receptor 7 (TLR7)- and Toll-like receptor 9 (TLR9)-stimulated PDC. Dinoprostone 40-56 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 20067543-2 2009 Here we demonstrate that tumour-derived prostaglandin E2 (PGE(2)) and transforming growth factor-beta (TGF-beta) increase interleukin-8 (IL-8) but synergistically inhibit interferon-alpha (IFN-alpha) and tumour necrosis factor (TNF) production of Toll-like receptor 7 (TLR7)- and Toll-like receptor 9 (TLR9)-stimulated PDC. Prostaglandins E 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 122-135 20067543-2 2009 Here we demonstrate that tumour-derived prostaglandin E2 (PGE(2)) and transforming growth factor-beta (TGF-beta) increase interleukin-8 (IL-8) but synergistically inhibit interferon-alpha (IFN-alpha) and tumour necrosis factor (TNF) production of Toll-like receptor 7 (TLR7)- and Toll-like receptor 9 (TLR9)-stimulated PDC. Prostaglandins E 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 19787256-7 2009 These findings suggest that Cepharanthine can suppress angiogenesis and growth of OSCC cells by inhibiting expression of VEGF and IL-8 involved in the blockade of NF-kappaB activity. cepharanthine 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 20134045-7 2009 Inhibition of NF-kappaB with curcumin or parthenolide resulted in a decrease of IL-8 secretion. Curcumin 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 19726162-0 2009 Nicotinamide inhibits Propionibacterium acnes-induced IL-8 production in keratinocytes through the NF-kappaB and MAPK pathways. Niacinamide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 19726162-7 2009 A luciferase reporter system assay was used to assess nicotinamide activity with the IL-8 promoter in transfected keratinocytes. Niacinamide 54-66 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 19726162-9 2009 RESULTS: Nicotinamide significantly decreased IL-8 production in a dose-dependent manner, decreasing both mRNA and protein levels for this chemokine in immortalized HaCaT cells and primary keratinocytes. Niacinamide 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19726162-10 2009 P. acnes-induced IL-8 promoter activation seemed to be downregulated by nicotinamide, which inhibited IkappaB degradation and the phosphorylation of ERK and JNK MAP kinases. Niacinamide 72-84 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 19726162-11 2009 CONCLUSION: Our results indicate that nicotinamide inhibits IL-8 production through the NF-kappaB and MAPK pathways in an in vitro keratinocytes/P. Niacinamide 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 20134045-7 2009 Inhibition of NF-kappaB with curcumin or parthenolide resulted in a decrease of IL-8 secretion. parthenolide 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 19525101-7 2009 RESULTS: Dexamethasone enhanced the phagocytic capacity of A549 cells and inhibited the production of IL-6 and IL-8 from A549 cells stimulated by LPS. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 19668110-9 2009 In PBMO, interaction with autologous apoptotic neutrophils reduced LPS-induced IL-8 production whereas it was enhanced in CBMO. pbmo 3-7 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 19525101-8 2009 Interestingly, aminophylline and terbutaline could not only down-regulate the ingestion of apoptotic eosinophils by A549 cells in a time- and dose-dependent manner, but also decrease IL-6 and IL-8 secretion by A549 cells induced by LPS. Aminophylline 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 19525101-8 2009 Interestingly, aminophylline and terbutaline could not only down-regulate the ingestion of apoptotic eosinophils by A549 cells in a time- and dose-dependent manner, but also decrease IL-6 and IL-8 secretion by A549 cells induced by LPS. Terbutaline 33-44 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 19713110-1 2009 We describe herein a novel series of 3-amino-4-hydrazine-cyclobut-3-ene-1,2-diones as potent and selective inhibitors against the CXCR2 chemokine receptor and IL-8-mediated chemotaxis of a CXCR2-expressing cell line. 3-amino-4-hydrazine-cyclobut-3-ene-1,2-diones 37-82 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 19525101-9 2009 CONCLUSIONS: The present study showed that all of the investigated anti-asthmatic drugs including dexamethasone, aminophylline and terbutaline play an anti-inflammatory effect by decreasing the release of IL-6 and IL-8 induced by LPS. Dexamethasone 98-111 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 19525101-9 2009 CONCLUSIONS: The present study showed that all of the investigated anti-asthmatic drugs including dexamethasone, aminophylline and terbutaline play an anti-inflammatory effect by decreasing the release of IL-6 and IL-8 induced by LPS. Aminophylline 113-126 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 19525101-9 2009 CONCLUSIONS: The present study showed that all of the investigated anti-asthmatic drugs including dexamethasone, aminophylline and terbutaline play an anti-inflammatory effect by decreasing the release of IL-6 and IL-8 induced by LPS. Terbutaline 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 19845437-5 2009 The serum half-life was estimated as being between 2 and 4 h. Prednisolone exhibits near complete inhibition of the cytokines TNF-alpha, IL-1beta, IL-6 and IL-8 with very similar IC50 estimates from 0.09 to 0.16 microg ml(-1) (from 0.24 to 0.44 microM). Prednisolone 62-74 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 19607809-3 2009 Both OA-NO(2) and LNO(2) prevented TNFalpha-stimulated release of the cytokines, IL-6, IL-8, IL-12/p40, IFNgamma, MCP-1, and IP-10, and inhibited NF-kappaB activation. L-Leucyl-Hydroxylamine 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 19846942-6 2009 Doxycycline (5 microg/ml) below the cytotoxic level suppressed endogenous and paclitaxel-induced IL-8 expression. Paclitaxel 78-88 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 19577291-6 2009 After 6 and 18 h of incubation HA and beta-TCP caused a quite similar induction of TNF-alpha, IL-1beta and IL-8. beta-tricalcium phosphate 38-46 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 19887723-2 2009 The aim of this study was to determine the effect of low level sodium fluoride (NaF) on the proliferation and migration of epithelial cells in vitro. Sodium Fluoride 63-78 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 19887723-7 2009 Quantitative real-time PCR revealed that low concentration of NaF up-regulated fibronectin mRNA expression in fluoride-treated cells compared with controls. Fluorides 110-118 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 19847291-9 2009 This was concomitant with increased IL-8 synthesis and cPLA2alpha activation, ultimately resulting in eicosanoid (PGE2 and LTB4) overproduction. Eicosanoids 102-112 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 19847291-9 2009 This was concomitant with increased IL-8 synthesis and cPLA2alpha activation, ultimately resulting in eicosanoid (PGE2 and LTB4) overproduction. Dinoprostone 114-118 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 19847291-10 2009 DRM destabilizing agent methyl-beta-cyclodextrin induced further cPLA2alpha activation and eicosanoid release, but inhibited IL-8 synthesis. methyl-beta-cyclodextrin 24-48 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 19835594-8 2009 While cells pre-treated with cytokines alone exhibited significantly enhanced IL-8 and CCL20 secretion following Pam3CSK4, mean IL-8 and CCL20 release decreased in Pam3CSK4 stimulated cells following cytokines + dex pre-treatment. Dexamethasone 212-215 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 19846942-3 2009 We also investigated the effect of doxycycline on expression of a potent proangiogenic factor, interleukin (IL)-8. Doxycycline 35-46 C-X-C motif chemokine ligand 8 Homo sapiens 95-113 19846942-6 2009 Doxycycline (5 microg/ml) below the cytotoxic level suppressed endogenous and paclitaxel-induced IL-8 expression. Doxycycline 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 19846942-8 2009 CONCLUSION: These data suggest that doxycycline exerts its antitumor effect by activating proapoptotic genes, inhibiting IL-8 expression, and suppressing antiapoptotic genes. Doxycycline 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 19632157-5 2009 We also show that RA patients produced anti-IL-8 autoantibodies and that their levels dropped after RTX treatment. resiniferatoxin 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 19632157-6 2009 Moreover, we identified antibody-IL-8 immune complexes in the synovial fluid and serum of RA patients, and found that the amount of these complexes decreased after the administration of RTX. resiniferatoxin 186-189 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 19654006-9 2009 Treatment of neutrophils with apyrase (catalyses the hydrolysis of ATP to yield AMP) and suramin (P2-receptor antagonist) abrogated the release of CXCL8 and elastase induced by cigarette smoke extract and exogenous ATP. Adenosine Triphosphate 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 147-152 19654006-9 2009 Treatment of neutrophils with apyrase (catalyses the hydrolysis of ATP to yield AMP) and suramin (P2-receptor antagonist) abrogated the release of CXCL8 and elastase induced by cigarette smoke extract and exogenous ATP. Adenosine Monophosphate 80-83 C-X-C motif chemokine ligand 8 Homo sapiens 147-152 19735076-6 2009 In addition, IL-8 secretion was markedly diminished by the non-selective P2 receptor antagonists reactive blue 2 and suramin, and by a selective P2Y(6) antagonist, MRS2578. Cibacron Blue F 3GA 97-112 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19654006-9 2009 Treatment of neutrophils with apyrase (catalyses the hydrolysis of ATP to yield AMP) and suramin (P2-receptor antagonist) abrogated the release of CXCL8 and elastase induced by cigarette smoke extract and exogenous ATP. Suramin 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 147-152 19735076-6 2009 In addition, IL-8 secretion was markedly diminished by the non-selective P2 receptor antagonists reactive blue 2 and suramin, and by a selective P2Y(6) antagonist, MRS2578. Suramin 117-124 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19654006-9 2009 Treatment of neutrophils with apyrase (catalyses the hydrolysis of ATP to yield AMP) and suramin (P2-receptor antagonist) abrogated the release of CXCL8 and elastase induced by cigarette smoke extract and exogenous ATP. Adenosine Triphosphate 215-218 C-X-C motif chemokine ligand 8 Homo sapiens 147-152 19589946-5 2009 CD clinical activity correlates directly with B cell expression of IL-8 and TLR2, suggesting a positive relationship between these B cell inflammatory mediators and disease pathogenesis. Cadmium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 20074471-3 2009 The aim of this study is to investigate whether tetrabromofluorecin, commonly know as eosin, a classical compound traditionally topically used in psoriasis for its presumed anti-inflammatory activities, is able to modulate the production of TNF-alpha, IL-6 and IL-8 that are recognized as the most active and characterized cytokines in the pathogenesis of this skin disorder. tetrabromofluorecin 48-67 C-X-C motif chemokine ligand 8 Homo sapiens 261-265 20074471-3 2009 The aim of this study is to investigate whether tetrabromofluorecin, commonly know as eosin, a classical compound traditionally topically used in psoriasis for its presumed anti-inflammatory activities, is able to modulate the production of TNF-alpha, IL-6 and IL-8 that are recognized as the most active and characterized cytokines in the pathogenesis of this skin disorder. Eosine Yellowish-(YS) 86-91 C-X-C motif chemokine ligand 8 Homo sapiens 261-265 20074471-8 2009 The expression and production of TNFalpha, IL-8 and IL-6 were dramatically reduced in presence of eosin 0.05% and 0.02% and the action of eosin was more pronounced on TNF-alpha. Eosine Yellowish-(YS) 98-103 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 19362013-14 2009 The PV/PA ratio of interleukin-8 and interleukin-10 increased after the restoration of the pulmonary circulation in the sufentanil group but decreased in the sevoflurane group. Sufentanil 120-130 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 19362013-14 2009 The PV/PA ratio of interleukin-8 and interleukin-10 increased after the restoration of the pulmonary circulation in the sufentanil group but decreased in the sevoflurane group. Sevoflurane 158-169 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 19740380-9 2009 Superoxide release from neutrophils was measured by the reduction of ferricytochrome C, degranulation by the conversion of a synthetic colour substrate, cytokine release by interleukin-8 enzyme-linked immunosorbent assay, and adhesion by a flow-based adhesion assay. Superoxides 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 173-186 19626664-0 2009 Glucosamine inhibits IL-1beta-mediated IL-8 production in prostate cancer cells by MAPK attenuation. Glucosamine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 19626664-4 2009 Glucosamine is widely regarded as an anti-inflammatory agent and thus we hypothesized that if IL-1beta activated IL-8 production in prostate cancer cells, then glucosamine ought to blunt such an effect. Glucosamine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 19626664-5 2009 Three prostate cancer cell lines, DU-145, PC-3, and LNCaP, were used to evaluate the effects of IL-1beta and glucosamine on IL-8 expression using ELISA and RT-PCR analyses. Glucosamine 109-120 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 19626664-7 2009 Glucosamine significantly inhibited IL-1beta-induced IL-8 secretion. Glucosamine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 19626664-8 2009 IL-8 appeared to induce LNCaP cell proliferation by MTT assay; involvement of IL-8 in IL-1beta-dependent PC-3 cell migration was demonstrated by wound-healing and transwell migration assays. monooxyethylene trimethylolpropane tristearate 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19626664-12 2009 In this context, glucosamine appears to inhibit IL-1beta-mediated activation of MAPKs and therefore reduces IL-8 production; this, in turn, attenuates cell proliferation/migration. Glucosamine 17-28 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 19745762-10 2009 Gangliosides suppressed infant bowel production of nitric oxide, leukotriene B4, prostaglandin E2, hydrogen peroxide, interleukin-1beta, interleukin-6, and interleukin-8 in response to LPS exposure and hypoxia. Gangliosides 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 156-169 19699525-11 2009 Interestingly, IL-8 mRNA was induced by cycloheximide treatment and RANTES showed reduced mRNA but increased protein expression by antibody stimulation. Cycloheximide 40-53 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 19732956-9 2009 In patients treated with methotrexate for active inflammatory arthritis, a reduction in NR4A2 synovial tissue levels correlate significantly (n=10, r=0.73, p=0.002) with changes in IL-8 expression. Methotrexate 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 19555716-11 2009 Macrolides have shown great promise in their ability to reduce airway inflammation, and can reduce airway neutrophils, levels of CXCL8 and neutrophil proteases in the airways. Macrolides 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 129-134 19794965-0 2009 A(2B) and A(3) adenosine receptors modulate vascular endothelial growth factor and interleukin-8 expression in human melanoma cells treated with etoposide and doxorubicin. Etoposide 145-154 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 19794965-0 2009 A(2B) and A(3) adenosine receptors modulate vascular endothelial growth factor and interleukin-8 expression in human melanoma cells treated with etoposide and doxorubicin. Doxorubicin 159-170 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 19794965-5 2009 We have examined whether the DNA-damaging agents etoposide (VP-16) and doxorubicin can affect IL-8, VEGF, and HIF-1 expressions in human melanoma cancer cells. Etoposide 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 19794965-5 2009 We have examined whether the DNA-damaging agents etoposide (VP-16) and doxorubicin can affect IL-8, VEGF, and HIF-1 expressions in human melanoma cancer cells. Etoposide 60-65 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 19794965-5 2009 We have examined whether the DNA-damaging agents etoposide (VP-16) and doxorubicin can affect IL-8, VEGF, and HIF-1 expressions in human melanoma cancer cells. Doxorubicin 71-82 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 19788733-3 2009 Here we study the role of the cyclic AMP (cAMP) effectors protein kinase A (PKA) and exchange proteins directly activated by cAMP (Epac1 and Epac2) in the bradykinin-induced IL-8 release from a human airway smooth muscle cell line and the underlying molecular mechanisms of this response. Cyclic AMP 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 19591856-0 2009 HuR/ELAVL1 RNA binding protein modulates interleukin-8 induction by muco-active ribotoxin deoxynivalenol. deoxynivalenol 90-104 C-X-C motif chemokine ligand 8 Homo sapiens 41-54 19591856-3 2009 We investigated the effects of ribotoxin deoxynivalenol (DON) on HuR translocation and its involvement in the regulation of the pro-inflammatory interleukin-8 (IL-8) mRNA stability. deoxynivalenol 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 145-158 19591856-3 2009 We investigated the effects of ribotoxin deoxynivalenol (DON) on HuR translocation and its involvement in the regulation of the pro-inflammatory interleukin-8 (IL-8) mRNA stability. deoxynivalenol 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 19591856-5 2009 Moreover, the interference with HuR protein production suppressed ribotoxic DON-induced IL-8 secretion and its mRNA stability. deoxynivalenol 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 19591856-7 2009 Partly in terms of IL-8-modulating transcription factors, HuR protein was demonstrated to be positively and negatively associated with DON-induced early growth response gene 1 (EGR-1) and activating transcription factor 3 (ATF3), respectively. deoxynivalenol 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 19788733-16 2009 Treatment of the cells with toxin B-1470 and U0126 significantly reduced bradykinin-induced IL-8 release alone or in combination with the activators of PKA and Epac. Boron 34-35 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 19788733-16 2009 Treatment of the cells with toxin B-1470 and U0126 significantly reduced bradykinin-induced IL-8 release alone or in combination with the activators of PKA and Epac. U 0126 45-50 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 19788733-3 2009 Here we study the role of the cyclic AMP (cAMP) effectors protein kinase A (PKA) and exchange proteins directly activated by cAMP (Epac1 and Epac2) in the bradykinin-induced IL-8 release from a human airway smooth muscle cell line and the underlying molecular mechanisms of this response. Cyclic AMP 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 19788749-8 2009 RESULTS: The spontaneous IL-8 and GM-CSF release was significantly reduced with MXF (8 mg/l) by 37 +/- 20% and 45 +/- 31%, respectively (both p < 0.01). Moxifloxacin 80-83 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 19788733-3 2009 Here we study the role of the cyclic AMP (cAMP) effectors protein kinase A (PKA) and exchange proteins directly activated by cAMP (Epac1 and Epac2) in the bradykinin-induced IL-8 release from a human airway smooth muscle cell line and the underlying molecular mechanisms of this response. Cyclic AMP 125-129 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 19788749-9 2009 IL-8 release in TNF-alpha stimulated hu-BEC decreased by 16 +/- 8% (p < 0.05) with AZM (1.5 mg/l). Azithromycin 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19788733-4 2009 METHODS: IL-8 release was assessed via ELISA under basal condition and after stimulation with bradykinin alone or in combination with fenoterol, the Epac activators 8-pCPT-2"-O-Me-cAMP and Sp-8-pCPT-2"-O-Me-cAMPS, the PKA activator 6-Bnz-cAMP and the cGMP analog 8-pCPT-2"-O-Me-cGMP. Fenoterol 134-143 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 19788733-4 2009 METHODS: IL-8 release was assessed via ELISA under basal condition and after stimulation with bradykinin alone or in combination with fenoterol, the Epac activators 8-pCPT-2"-O-Me-cAMP and Sp-8-pCPT-2"-O-Me-cAMPS, the PKA activator 6-Bnz-cAMP and the cGMP analog 8-pCPT-2"-O-Me-cGMP. 8-pCPT-2'-O-Me-cAMP 165-184 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 19788733-4 2009 METHODS: IL-8 release was assessed via ELISA under basal condition and after stimulation with bradykinin alone or in combination with fenoterol, the Epac activators 8-pCPT-2"-O-Me-cAMP and Sp-8-pCPT-2"-O-Me-cAMPS, the PKA activator 6-Bnz-cAMP and the cGMP analog 8-pCPT-2"-O-Me-cGMP. sp-8-pcpt-2"-o-me-camps 189-212 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 19648110-4 2009 Since NF-kappaB-dependent transcription and IL-8 protein, mRNA, and unspliced RNA (a surrogate of transcription rate) are sensitive to p38 MAPK inhibitors (SB203580 and SB239063), we explored the role of MKP-1 in repression of these outputs. SB 203580 156-164 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 19788733-4 2009 METHODS: IL-8 release was assessed via ELISA under basal condition and after stimulation with bradykinin alone or in combination with fenoterol, the Epac activators 8-pCPT-2"-O-Me-cAMP and Sp-8-pCPT-2"-O-Me-cAMPS, the PKA activator 6-Bnz-cAMP and the cGMP analog 8-pCPT-2"-O-Me-cGMP. Bz-Camp 232-242 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 19648110-4 2009 Since NF-kappaB-dependent transcription and IL-8 protein, mRNA, and unspliced RNA (a surrogate of transcription rate) are sensitive to p38 MAPK inhibitors (SB203580 and SB239063), we explored the role of MKP-1 in repression of these outputs. SB 239063 169-177 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 19648110-5 2009 Repression of TNFalpha-induced p38 MAPK phosphorylation, NF-kappaB-dependent transcription, and IL-8 expression by dexamethasone are sensitive to transcriptional or translational inhibitors. Dexamethasone 115-128 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 19788733-4 2009 METHODS: IL-8 release was assessed via ELISA under basal condition and after stimulation with bradykinin alone or in combination with fenoterol, the Epac activators 8-pCPT-2"-O-Me-cAMP and Sp-8-pCPT-2"-O-Me-cAMPS, the PKA activator 6-Bnz-cAMP and the cGMP analog 8-pCPT-2"-O-Me-cGMP. Cyclic GMP 251-255 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 19788733-4 2009 METHODS: IL-8 release was assessed via ELISA under basal condition and after stimulation with bradykinin alone or in combination with fenoterol, the Epac activators 8-pCPT-2"-O-Me-cAMP and Sp-8-pCPT-2"-O-Me-cAMPS, the PKA activator 6-Bnz-cAMP and the cGMP analog 8-pCPT-2"-O-Me-cGMP. 8-pcpt-2"-o-me-cgmp 263-282 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 19788733-11 2009 RESULTS: The beta2-agonist fenoterol augmented release of IL-8 by bradykinin. Fenoterol 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 19788733-12 2009 The PKA activator 6-Bnz-cAMP and the Epac activator 8-pCPT-2"-O-Me-cAMP significantly increased bradykinin-induced IL-8 release. Bz-Camp 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19788733-12 2009 The PKA activator 6-Bnz-cAMP and the Epac activator 8-pCPT-2"-O-Me-cAMP significantly increased bradykinin-induced IL-8 release. 8-pcpt-2"-o-me 52-66 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19788733-12 2009 The PKA activator 6-Bnz-cAMP and the Epac activator 8-pCPT-2"-O-Me-cAMP significantly increased bradykinin-induced IL-8 release. Cyclic AMP 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19372002-8 2009 However, such an acceleration is markedly suppressed by introducing NaF into the reaction system since NaF forms a complex with Fe(III). ferric sulfate 128-135 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 19372002-8 2009 However, such an acceleration is markedly suppressed by introducing NaF into the reaction system since NaF forms a complex with Fe(III). ferric sulfate 128-135 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 19422399-4 2009 KEY RESULTS: In equilibrium saturation binding studies, SB265610 depressed the maximal binding of [(125)I]-interleukin-8 ([(125)I]-IL-8) without affecting the K(d). 1-(2-bromophenyl)-3-(7-cyano-3H-benzotriazol-4-yl)urea 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 107-120 19647751-3 2009 KEY FINDINGS: We showed that gAd induces the expression of a number of genes using PCR arrays, including MCP-1, VCAM-1, E-selectin, IL-6, and IL-8, all of which have been previously shown to be associated with adiponectin, as well as SOD2, PAI-1, and CSF2, which is a new finding. ganoderic acid D 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 19753313-9 2009 Treatment with 100 microg/ml cis-UCA completely suppressed IL-6 and IL-8 secretion, decreased caspase-3 activity, and improved cell viability against UV-B irradiation. cis-Urocanic acid 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 19422399-4 2009 KEY RESULTS: In equilibrium saturation binding studies, SB265610 depressed the maximal binding of [(125)I]-interleukin-8 ([(125)I]-IL-8) without affecting the K(d). 1-(2-bromophenyl)-3-(7-cyano-3H-benzotriazol-4-yl)urea 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 19422399-7 2009 In functional experiments, SB265610 caused a rightward shift of the concentration-response curves to IL-8 and growth-related oncogene alpha, but also a reduction in maximal response elicited by each agonist. 1-(2-bromophenyl)-3-(7-cyano-3H-benzotriazol-4-yl)urea 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 101-139 19839871-8 2009 The result of ELISA also showed the release of IL-6 and IL-8 can be inhibited by hydrocortisone. Hydrocortisone 81-95 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 19941760-8 2009 Conversely, the adhesive resin and formocresol stimulated the production of IL-8, and did not stimulate IL-l beta. formocresol 35-46 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 19694614-5 2009 In vitro studies using phorbol 12-myristyl 13-acetate (PMA) stimulated macrophage-like THP-1 (mTHP-1) cells were focused on cytotoxicity of both polymers and particles, and their potential to stimulate IL-8 release via the TLR-2 pathway. phorbol 12-myristyl 13-acetate 23-53 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 19694614-5 2009 In vitro studies using phorbol 12-myristyl 13-acetate (PMA) stimulated macrophage-like THP-1 (mTHP-1) cells were focused on cytotoxicity of both polymers and particles, and their potential to stimulate IL-8 release via the TLR-2 pathway. Tetradecanoylphorbol Acetate 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 19740321-9 2009 Poly(I:C) induced a small increase in IL-1beta, IL-6 and IL-8 production in HNECs, while Pam(3)CSK(4) increased viability. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 19450704-5 2009 Treating HeLa cells with the calcium chelator BAPTA-AM or with D-BAPTA-AM, a derivative with greatly reduced Ca(2+) chelating activity, yielded strong evidence that BAPTA-AM does not affect invasion and inhibits IL-8 secretion by a calcium-dependent mechanism. d-bapta-am 63-73 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 19928254-1 2009 In the present work, aligned TiO2 nanotubes have been synthesized by a simple method of electrochemical anodization of high purity, well cleaned, etched and ultrasonicated Ti-sheet (Purity approximately 99.99%) in a fluoride mediated electrolytic media consisting of a solution of 0.14 M NaF and a solution of 0.5 M/1.0 M H3PO4. titanium dioxide 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 288-291 19500686-0 2009 Norepinephrine-dependently released Dr fimbriae of diffusely adhering Escherichia coli strain IH11128 promotes a mitogen-activated protein kinase ERK1/2-dependent production of pro-inflammatory cytokine, IL-8 in human intestinal Caco-2/TC7 cells. Norepinephrine 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 19740260-9 2009 Significant results in univariate and multivariate analysis of the association between biomarkers and BODE components were: serum MCP-1 correlated with FEV(1)% and 6MWD; serum IL-8 and GRO-alpha correlated with steroid use; serum TNF-alpha correlated with steroid use and FEV(1)%; and serum MMP-9 correlated with MMRC dyspnoea scale. Steroids 211-218 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 19703242-9 2009 In conclusion, L. reuteri RC-14 alone and together with L. rhamnosus GR-1 have the potential to inhibit the yeast growth and their CFS may up-regulate IL-8 and IP-10 secretion by VK2/E6E7 cells, which could possibly have played an important role in helping to clear VVC in vivo. 1,1-dichloro-1-fluoroethane 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 19668862-7 2009 Reporter systems with segments of the IL-8 promoter showed a specific activation in response to hm-sulfated polysaccharides with lower pathophysiological potential in vivo and provided a better classification of CGN-variants than cytotoxicity assays in vitro. Polysaccharides 108-123 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 19668862-8 2009 IL-8 reporter systems can be used for discerning between the effects of sulfated polysaccharides in vivo. Polysaccharides 81-96 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19564644-7 2009 Medroxyprogesterone acetate significantly suppressed LPS-induced production of interleukin 1b (IL-1b), IL-6, and IL-8 in vitro (P < .05). Medroxyprogesterone Acetate 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 19781372-8 2009 In addition, preincubation of EPCs with SB203580, an inhibitor of p38 mitogen-activated protein kinase (MAPK) decreased CRP inhibition of IL-8 mRNA expression at 12 hours in EPCs. SB 203580 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 19651324-12 2009 Additionally, SM upregulates many inflammatory mediators including interleukin (IL)-1alpha, IL-1beta, IL-6, IL-8, tumor necrosis factor-alpha (TNF-alpha) and others. Mustard Gas 14-16 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 19709445-11 2009 The IL-8 induced-IL-8 mRNA expression was inhibited by PD98059 (a MEK inhibitor) or SB203580 (a p38 MAPK inhibitor). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 55-62 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 19709445-11 2009 The IL-8 induced-IL-8 mRNA expression was inhibited by PD98059 (a MEK inhibitor) or SB203580 (a p38 MAPK inhibitor). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 55-62 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 19709445-11 2009 The IL-8 induced-IL-8 mRNA expression was inhibited by PD98059 (a MEK inhibitor) or SB203580 (a p38 MAPK inhibitor). SB 203580 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 19709445-11 2009 The IL-8 induced-IL-8 mRNA expression was inhibited by PD98059 (a MEK inhibitor) or SB203580 (a p38 MAPK inhibitor). SB 203580 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 19709445-13 2009 The inhibitory effect of IL-8 was eliminated by either PD 98059 or SB203580. SB 203580 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 19540326-0 2009 Tetramethylpyrazine suppresses interleukin-8 expression in LPS-stimulated human umbilical vein endothelial cell by blocking ERK, p38 and nulear factor-kappaB signaling pathways. tetramethylpyrazine 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 19540326-1 2009 AIM OF THE STUDY: To determine the anti-inflammatory effects of Tetramethylpyrazine (TMP) and to investigate the inhibitory effect of TMP on IL-8 production in human umbilical vein endothelial cells (HUVECs) induced by LPS might be mediated by inhibiting p38, ERK and NF-kappaB signaling pathways. tetramethylpyrazine 134-137 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 19540326-6 2009 RESULTS: TMP inhibits LPS-induced IL-8 production in HUVECs at both the protein and mRNA levels, suggesting that TMP has an antiinflammatory effect on endothelial cells. tetramethylpyrazine 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 19540326-6 2009 RESULTS: TMP inhibits LPS-induced IL-8 production in HUVECs at both the protein and mRNA levels, suggesting that TMP has an antiinflammatory effect on endothelial cells. tetramethylpyrazine 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 19540326-10 2009 CONCLUSIONS: The inhibitory effect of TMP on the LPS-induced IL-8 production is mediated by the NF-kappaB-dependent pathway, and TMP also separately affects the ERK and p38 MAPK pathway. tetramethylpyrazine 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 19691415-3 2009 In the present work, we perform simulations on proteins Naf-BBL, QNND-BBL, CI2, and SH3 with the Go model and compare their different folding behaviors. N-Carbobenzyloxy-L-alanine 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 19635923-5 2009 In Boyden chamber assays, alphabetaMeATP provoked chemokinesis and enhanced formylated peptide- and IL-8-induced chemotaxis of human neutrophils. alpha,beta-methyleneadenosine 5'-triphosphate 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 19376214-4 2009 NaF-induced accumulation of COX-2 transcript was abolished by actinomycin D, but not cycloheximide. Dactinomycin 62-75 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 19376214-4 2009 NaF-induced accumulation of COX-2 transcript was abolished by actinomycin D, but not cycloheximide. Cycloheximide 85-98 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 19376214-5 2009 The level of prostaglandin E(2), a major product of COX enzymes, increased in response to NaF exposure, and its production was abolished by the selective COX-2 inhibitor NS-398. Dinoprostone 13-31 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 19376214-5 2009 The level of prostaglandin E(2), a major product of COX enzymes, increased in response to NaF exposure, and its production was abolished by the selective COX-2 inhibitor NS-398. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 170-176 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 19376214-6 2009 Phosphorylated forms of mitogen-activated protein kinases (MAPKs)-including extracellular signal-regulated protein kinase (ERK), c-Jun NH(2)-terminal kinase, and p38-increased after NaF exposure, while treatment with the MAPK/ERK kinase inhibitor U0126 and the p38 inhibitor SB203580 markedly suppressed COX-2 expression. U 0126 247-252 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 19376214-6 2009 Phosphorylated forms of mitogen-activated protein kinases (MAPKs)-including extracellular signal-regulated protein kinase (ERK), c-Jun NH(2)-terminal kinase, and p38-increased after NaF exposure, while treatment with the MAPK/ERK kinase inhibitor U0126 and the p38 inhibitor SB203580 markedly suppressed COX-2 expression. SB 203580 275-283 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 19376214-7 2009 Furthermore, NaF-induced COX-2 expression was markedly suppressed by the Src family kinase (SFK) inhibitor PP2, but only partially suppressed by the epidermal growth factor receptor (EGFR) inhibitor PD153035. 4-((3-bromophenyl)amino)-6,7-dimethoxyquinazoline 199-207 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 19578117-4 2009 On the other hand, loop 2 of IL-8 closely resembles a surface-exposed sequence of the VWF propeptide, the region of VWF that directs sorting of the protein to WPB. propeptide 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 19558546-7 2009 KEY RESULTS: BGMP up-regulated the secretion of TNF, IL-1beta and IL-8 in a concentration-dependent fashion. bgmp 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 19525388-10 2009 Ox-AT generated in the airway interacts directly with epithelial cells to release chemokines IL-8 and MCP-1, which in turn attracts macrophages and neutrophils into the airways. ox-at 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 19349075-6 2009 NHBC responded to PE particles by increasing the mRNA expression of several genes associated with osteoclast formation and activity (RANKL, IL-8 and M-CSF) and decreased the expression of the osteoclast antagonist, OPG. Polyethylene 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 19558546-9 2009 The secretion of IL-8 and specially TNF and IL-1beta was blocked by PD98059, SP600125, SB203580 and Bay11-7082, suggesting the involvement of the MAP kinases p38, c-Jun N-terminal kinase and ERK and particularly the NF-kappaB pathway, although IL-8 secretion was independent of p38. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 19558546-9 2009 The secretion of IL-8 and specially TNF and IL-1beta was blocked by PD98059, SP600125, SB203580 and Bay11-7082, suggesting the involvement of the MAP kinases p38, c-Jun N-terminal kinase and ERK and particularly the NF-kappaB pathway, although IL-8 secretion was independent of p38. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 19558546-9 2009 The secretion of IL-8 and specially TNF and IL-1beta was blocked by PD98059, SP600125, SB203580 and Bay11-7082, suggesting the involvement of the MAP kinases p38, c-Jun N-terminal kinase and ERK and particularly the NF-kappaB pathway, although IL-8 secretion was independent of p38. pyrazolanthrone 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 19558546-9 2009 The secretion of IL-8 and specially TNF and IL-1beta was blocked by PD98059, SP600125, SB203580 and Bay11-7082, suggesting the involvement of the MAP kinases p38, c-Jun N-terminal kinase and ERK and particularly the NF-kappaB pathway, although IL-8 secretion was independent of p38. pyrazolanthrone 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 19558546-9 2009 The secretion of IL-8 and specially TNF and IL-1beta was blocked by PD98059, SP600125, SB203580 and Bay11-7082, suggesting the involvement of the MAP kinases p38, c-Jun N-terminal kinase and ERK and particularly the NF-kappaB pathway, although IL-8 secretion was independent of p38. SB 203580 87-95 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 19558546-9 2009 The secretion of IL-8 and specially TNF and IL-1beta was blocked by PD98059, SP600125, SB203580 and Bay11-7082, suggesting the involvement of the MAP kinases p38, c-Jun N-terminal kinase and ERK and particularly the NF-kappaB pathway, although IL-8 secretion was independent of p38. SB 203580 87-95 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 19527294-5 2009 Treatment of bronchial epithelial cells with LL-37 and the TLR3 agonist polyI:C resulted in synergistic increases in IL-8 release and cytotoxicity. Poly I-C 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 19622582-9 2009 AdEHCD40L induced apoptosis and S-phase cell cycle blockade while uniquely up-regulating the previously described proapoptotic elements tumor necrosis factor-related apoptosis-inducing ligand, Fas, and IL-8. adehcd40l 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 19638548-5 2009 RESULTS: The mean glucose concentrations for NaF-KOx samples and Li-Heparin samples were 5.7 mmol/l and 6.1 mmol/l, respectively, with a mean difference of 0.39 mmol/l. Glucose 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 19464389-4 2009 Hirsutenone attenuated the TNF-alpha-induced production of cytokine IL-8, prostaglandin E(2) and chemokine CCL27, and the formation of reactive oxygen/nitrogen species in keratinocytes. hirsutenone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 19464389-5 2009 Immunosuppressants (dexamethasone and cyclosporin A) inhibited the TNF-alpha-elicited formation of IL-8, prostaglandin E(2) and CCL27, but did not affect formation of reactive species. Dexamethasone 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 19464389-5 2009 Immunosuppressants (dexamethasone and cyclosporin A) inhibited the TNF-alpha-elicited formation of IL-8, prostaglandin E(2) and CCL27, but did not affect formation of reactive species. Cyclosporine 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 19842832-11 2009 These stimuli seem to activate mainly redox-sensitive transcription factors such as nuclear factor (NF)-kappa B and activator protein (AP)-1, both of which play a major role in the synthesis and secretion of chemotactic factors such as IL-8 and leukotriene B(4) (LTB(4)). Leukotriene B4 245-258 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 19507016-5 2009 In the transfection experiment, PD98059, a MEK1 inhibitor, decreased the transcription of IL-8 in a dose dependent pattern. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 19397752-9 2009 On day 5: IL-13, IL-7, IL-8 and MIP-1alpha concentrations were higher in dexamethasone-treated patients. Dexamethasone 73-86 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 19649202-8 2009 Finally, PD0325901 inhibited the production of the proangiogenic factors vascular endothelial growth factor and interleukin 8 at a transcriptional level. mirdametinib 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 19951500-6 2009 01); the level of IL-8 in sputum was significantly higher in severe asthmatics [2907.78 (331.67 - 3457.93) ng/L] than mild-moderate asthmatics [287.58 (130.75-656.84) ng/L] and healthy control subjects [179.2 (58.55-346.59) ng/L] (P < 0.01); the percentages of neutrophilic apoptosis respectively cultured with LPS [(10.57 +/- 1.97)%], severe asthmatics supernatant [(11.82 +/- 2.96)%], IL-8 [(10.47 +/- 1.93)%], dexamethasone [(9.93 +/- 1.95)%], severe asthma supernatant + mifepristone [(12.15 +/- 2.86)%] in vitro were lower than that cultured with PBS [(17.98 +/- 2.27)%], healthy control supernatant [(17.37 +/- 2.50)%], mild-moderate asthmatics supernatant [(16.35 +/- 3.26)%], mifepristone [(17.89 +/- 2.38)%], and dexamethasone + mifepristone [(17.06 +/- 2.59)%] (P < 0.01). Dexamethasone 416-429 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 19400824-0 2009 Macrophage inflammatory protein-1beta and interleukin-8 associated with idiopathic steroid-sensitive nephrotic syndrome. Steroids 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 19646263-15 2009 Specifically, the cytotoxicity of Docetaxel, Staurosporine and Rapamycin increased significantly (>40% at IC50 dose) in IL-8 depleted cells as compared to that in C-siRNA transfected cells. Docetaxel 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 19646263-15 2009 Specifically, the cytotoxicity of Docetaxel, Staurosporine and Rapamycin increased significantly (>40% at IC50 dose) in IL-8 depleted cells as compared to that in C-siRNA transfected cells. Staurosporine 45-58 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 19646263-15 2009 Specifically, the cytotoxicity of Docetaxel, Staurosporine and Rapamycin increased significantly (>40% at IC50 dose) in IL-8 depleted cells as compared to that in C-siRNA transfected cells. Sirolimus 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 19951500-6 2009 01); the level of IL-8 in sputum was significantly higher in severe asthmatics [2907.78 (331.67 - 3457.93) ng/L] than mild-moderate asthmatics [287.58 (130.75-656.84) ng/L] and healthy control subjects [179.2 (58.55-346.59) ng/L] (P < 0.01); the percentages of neutrophilic apoptosis respectively cultured with LPS [(10.57 +/- 1.97)%], severe asthmatics supernatant [(11.82 +/- 2.96)%], IL-8 [(10.47 +/- 1.93)%], dexamethasone [(9.93 +/- 1.95)%], severe asthma supernatant + mifepristone [(12.15 +/- 2.86)%] in vitro were lower than that cultured with PBS [(17.98 +/- 2.27)%], healthy control supernatant [(17.37 +/- 2.50)%], mild-moderate asthmatics supernatant [(16.35 +/- 3.26)%], mifepristone [(17.89 +/- 2.38)%], and dexamethasone + mifepristone [(17.06 +/- 2.59)%] (P < 0.01). Mifepristone 478-490 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 19951500-6 2009 01); the level of IL-8 in sputum was significantly higher in severe asthmatics [2907.78 (331.67 - 3457.93) ng/L] than mild-moderate asthmatics [287.58 (130.75-656.84) ng/L] and healthy control subjects [179.2 (58.55-346.59) ng/L] (P < 0.01); the percentages of neutrophilic apoptosis respectively cultured with LPS [(10.57 +/- 1.97)%], severe asthmatics supernatant [(11.82 +/- 2.96)%], IL-8 [(10.47 +/- 1.93)%], dexamethasone [(9.93 +/- 1.95)%], severe asthma supernatant + mifepristone [(12.15 +/- 2.86)%] in vitro were lower than that cultured with PBS [(17.98 +/- 2.27)%], healthy control supernatant [(17.37 +/- 2.50)%], mild-moderate asthmatics supernatant [(16.35 +/- 3.26)%], mifepristone [(17.89 +/- 2.38)%], and dexamethasone + mifepristone [(17.06 +/- 2.59)%] (P < 0.01). Lead 555-558 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 19951500-6 2009 01); the level of IL-8 in sputum was significantly higher in severe asthmatics [2907.78 (331.67 - 3457.93) ng/L] than mild-moderate asthmatics [287.58 (130.75-656.84) ng/L] and healthy control subjects [179.2 (58.55-346.59) ng/L] (P < 0.01); the percentages of neutrophilic apoptosis respectively cultured with LPS [(10.57 +/- 1.97)%], severe asthmatics supernatant [(11.82 +/- 2.96)%], IL-8 [(10.47 +/- 1.93)%], dexamethasone [(9.93 +/- 1.95)%], severe asthma supernatant + mifepristone [(12.15 +/- 2.86)%] in vitro were lower than that cultured with PBS [(17.98 +/- 2.27)%], healthy control supernatant [(17.37 +/- 2.50)%], mild-moderate asthmatics supernatant [(16.35 +/- 3.26)%], mifepristone [(17.89 +/- 2.38)%], and dexamethasone + mifepristone [(17.06 +/- 2.59)%] (P < 0.01). Mifepristone 687-699 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 19951500-6 2009 01); the level of IL-8 in sputum was significantly higher in severe asthmatics [2907.78 (331.67 - 3457.93) ng/L] than mild-moderate asthmatics [287.58 (130.75-656.84) ng/L] and healthy control subjects [179.2 (58.55-346.59) ng/L] (P < 0.01); the percentages of neutrophilic apoptosis respectively cultured with LPS [(10.57 +/- 1.97)%], severe asthmatics supernatant [(11.82 +/- 2.96)%], IL-8 [(10.47 +/- 1.93)%], dexamethasone [(9.93 +/- 1.95)%], severe asthma supernatant + mifepristone [(12.15 +/- 2.86)%] in vitro were lower than that cultured with PBS [(17.98 +/- 2.27)%], healthy control supernatant [(17.37 +/- 2.50)%], mild-moderate asthmatics supernatant [(16.35 +/- 3.26)%], mifepristone [(17.89 +/- 2.38)%], and dexamethasone + mifepristone [(17.06 +/- 2.59)%] (P < 0.01). Dexamethasone 725-738 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 19951500-6 2009 01); the level of IL-8 in sputum was significantly higher in severe asthmatics [2907.78 (331.67 - 3457.93) ng/L] than mild-moderate asthmatics [287.58 (130.75-656.84) ng/L] and healthy control subjects [179.2 (58.55-346.59) ng/L] (P < 0.01); the percentages of neutrophilic apoptosis respectively cultured with LPS [(10.57 +/- 1.97)%], severe asthmatics supernatant [(11.82 +/- 2.96)%], IL-8 [(10.47 +/- 1.93)%], dexamethasone [(9.93 +/- 1.95)%], severe asthma supernatant + mifepristone [(12.15 +/- 2.86)%] in vitro were lower than that cultured with PBS [(17.98 +/- 2.27)%], healthy control supernatant [(17.37 +/- 2.50)%], mild-moderate asthmatics supernatant [(16.35 +/- 3.26)%], mifepristone [(17.89 +/- 2.38)%], and dexamethasone + mifepristone [(17.06 +/- 2.59)%] (P < 0.01). Mifepristone 687-699 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 19661014-7 2009 AZM increased PgLPS-induced IL-8 production dose-dependently, while AZM did not alter IL-6 and PGE2 productions. Azithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 19661014-0 2009 Macrolide antibiotics like azithromycin increase lipopolysaccharide-induced IL-8 production by human gingival fibroblasts. macrolide antibiotics 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 19623255-4 2009 At the same time, calcipotriol normalized the proinflammatory cytokine milieu and decreased interleukin (IL)-17A, IL-17F and IL-8 transcript abundance in lesional psoriatic skin. calcipotriene 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 19661014-0 2009 Macrolide antibiotics like azithromycin increase lipopolysaccharide-induced IL-8 production by human gingival fibroblasts. Azithromycin 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 19661014-7 2009 AZM increased PgLPS-induced IL-8 production dose-dependently, while AZM did not alter IL-6 and PGE2 productions. pglps 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 19661014-11 2009 However, the use of the inhibitors of cell signaling pathway failed to reveal the mechanism that AZM enhanced PgLPS-induced IL-8 production. Azithromycin 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 19661014-11 2009 However, the use of the inhibitors of cell signaling pathway failed to reveal the mechanism that AZM enhanced PgLPS-induced IL-8 production. pglps 110-115 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 19661014-13 2009 Because AZM increased LPS-induced IL-8 production by HGFs, the possibility is considered that neutrophils may be migrated to periodontal tissue and phagocytize the periodontopathic bacteria more efficiently. Azithromycin 8-11 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 19427879-5 2009 Inhibition experiments show that, at least for DNFB, p38 MAP kinase signalling controls compound-specific changes in CD54 expression and IL-8 release. Dinitrofluorobenzene 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 19539545-2 2009 MSA is a potential in vivo metabolite of reparixin, a specific inhibitor of the CXCL8 biological activity. methanesulfonamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 19539545-2 2009 MSA is a potential in vivo metabolite of reparixin, a specific inhibitor of the CXCL8 biological activity. reparixin 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 19450611-10 2009 Furthermore, when exposed to hypoxia for 48 h, the inhibitory effects of dexamethasone on LPS-stimulated IL-8 release were attenuated. Dexamethasone 73-86 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 19450615-0 2009 Nanoparticles up-regulate tumor necrosis factor-alpha and CXCL8 via reactive oxygen species and mitogen-activated protein kinase activation. Reactive Oxygen Species 68-91 C-X-C motif chemokine ligand 8 Homo sapiens 58-63 19450615-5 2009 Blockade of ROS generation with antioxidants significantly abrogated the QD-mediated TNF-alpha and CXCL8 expression in monocytes. Reactive Oxygen Species 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 19450615-6 2009 The induced ROS generation subsequently led to the activation of MAPKs, which were crucial for mRNA and protein expression of TNF-alpha and CXCL8. Reactive Oxygen Species 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 140-145 19324973-10 2009 These findings were corroborated and extended in experiments with cultured human bronchial epithelial cells in which ectoine inhibited nanoparticle-triggered cell signaling and IL-8 induction. ectoine 117-124 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 19417127-6 2009 To verify whether muscular NF-kappaB activity in human subjects is suppressed by PPARgamma activation, we examined the effect of 8 wk of rosiglitazone treatment on muscular gene expression of ICAM-1 and IL-8 in type 2 diabetes mellitus patients. Rosiglitazone 137-150 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 19594939-12 2009 The expression levels of IL-8, ICAM-1, IP-10, MCP-1, TNF-alpha and MMP-1 were significantly reduced after PC pre-treatment for at least two hours. Phosphatidylcholines 106-108 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 19575800-1 2009 BACKGROUND: Previously we showed that reduced availability of the essential amino acid tryptophan per se attenuates post-transcriptional control of interleukin (IL)-6 and IL-8 leading to hyperresponsive production of these inflammatory mediators by airway epithelial cells. essential amino acid tryptophan 66-97 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 19575800-2 2009 Availability of the non-essential amino acid arginine in the inflamed airway mucosa of patients with asthma is reduced markedly, but it is not known whether this can also lead to an exaggerated production of IL-6 and IL-8. Arginine 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 19575800-7 2009 RESULTS: For both NCI-H292 and NHBE cells, low arginine concentrations enhanced basal epithelial IL-6 and IL-8 production and synergized with TNF-alpha-induced IL-6 and IL-8 production. Arginine 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 19575800-7 2009 RESULTS: For both NCI-H292 and NHBE cells, low arginine concentrations enhanced basal epithelial IL-6 and IL-8 production and synergized with TNF-alpha-induced IL-6 and IL-8 production. Arginine 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 19575800-8 2009 Poly-L-arginine enhanced the stimulus-induced IL-6 and IL-8 production, however, blocking arginine uptake and the enhanced IL-6 and IL-8 production appeared unrelated. polyarginine 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 19575800-8 2009 Poly-L-arginine enhanced the stimulus-induced IL-6 and IL-8 production, however, blocking arginine uptake and the enhanced IL-6 and IL-8 production appeared unrelated. Arginine 7-15 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 19575800-9 2009 The exaggerated IL-6 and IL-8 production due to arginine deficiency and to poly-L-arginine depend on a post-transcriptional and a transcriptional process, respectively. polyarginine 75-90 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 18712273-4 2009 Dietary supplementation with 0.8% arginine increased the numbers of white blood cells and granulocytes, and gene expression of interleukin (IL)-8 in spleen. Arginine 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 127-145 18712273-5 2009 On Day 14, compared with control piglets, granulocyte numbers were greater but lymphocyte numbers were lower in piglets supplemented with 0.2 and 0.4% arginine, whereas splenic expression of IL-8 and tumor necrosis factor-alpha genes was increased in piglets supplemented with 0.8% arginine. Arginine 151-159 C-X-C motif chemokine ligand 8 Homo sapiens 191-227 18712273-5 2009 On Day 14, compared with control piglets, granulocyte numbers were greater but lymphocyte numbers were lower in piglets supplemented with 0.2 and 0.4% arginine, whereas splenic expression of IL-8 and tumor necrosis factor-alpha genes was increased in piglets supplemented with 0.8% arginine. Arginine 282-290 C-X-C motif chemokine ligand 8 Homo sapiens 191-227 19254160-4 2009 Interestingly, both hypoxia and DMOG attenuated IL-8 expression, and a similar effect has been obtained by adenoviral overexpression of the stable form of HIF-1alpha. dimethyloxallyl glycine 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 19059883-5 2009 In primary human airway epithelial cells, inhibition of NQO1 by dicumarol blocks ozone-induced F(2)-isoprostane production and IL-8 gene expression. Dicumarol 64-73 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 19059883-5 2009 In primary human airway epithelial cells, inhibition of NQO1 by dicumarol blocks ozone-induced F(2)-isoprostane production and IL-8 gene expression. Ozone 81-86 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 19415233-7 2009 RESULTS: Treatment of LPS-stimulated human islets with the synthetic LXR agonist GW3965 (1 micromol/l) for 24 h reduced mRNA and protein levels of selected pro-inflammatory cytokines (IL-8, monocyte chemotactic protein-1 and tissue factor). GW 3965 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 19318678-7 2009 The major bile acid, chenodeoxycholic acid, stimulated alveolar epithelial cells to increase IL-8 production at both the messenger RNA and protein level through p38 and c-Jun N-terminal kinase (JNK) activation. Bile Acids and Salts 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 19318678-7 2009 The major bile acid, chenodeoxycholic acid, stimulated alveolar epithelial cells to increase IL-8 production at both the messenger RNA and protein level through p38 and c-Jun N-terminal kinase (JNK) activation. Chenodeoxycholic Acid 21-42 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 19318678-8 2009 The selective p38 and JNK inhibitors, as well as dexamethasone, successfully inhibited IL-8 production. Dexamethasone 49-62 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 19132727-2 2009 Titanium particles have previously been shown to induce IL-8 and MCP-1 secretion in osteoblasts. Titanium 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 19542452-6 2009 Transcriptional blockade studies using actinomycin D revealed a similar degradation rate of IL-8/CXCL8 mRNA in the presence or absence of NE, suggesting an involvement at the transcription level. Dactinomycin 39-52 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 19558223-7 2009 Finally, the release of a proinflammatory cytokine (i.e. IL-8) by the exposed cells similarly increased with cell iron concentration. Iron 114-118 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 19916466-1 2009 This paper discusses the preparation of titania nanotubes by anodisation of Ti in a glycerol-based electrolyte containing 0.5% wt of sodium fluoride (NaF). Sodium Fluoride 133-148 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 19132727-6 2009 We demonstrate that cobalt ions rapidly induce the protein secretion of IL-8 and MCP-1 in primary human osteoblasts. Cobalt 20-26 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 19132727-10 2009 In aggregate these data demonstrate that cobalt ions can activate transcription of the chemokine genes IL-8 and MCP-1 in primary human osteoblasts. Cobalt 41-47 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 19522763-4 2009 In addition, poly I:C treatment inhibited cell growth and triggered up-regulation of IL-12p40, IL-8 and Il-1alpha in Detroit 562 cell line. Poly I-C 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 19184985-8 2009 These data suggest that hypoxia induces biosynthesis of PGF(2alpha), which then activates HGF and IL-8 expression. Prostaglandins F 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 19184985-9 2009 The results provide a reasonable explanation of how PGF(2alpha), HGF and IL-8 exert their effects on cancer cell metastasis. Prostaglandins F 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 19434061-7 2009 Endogenous and TNF-alpha-induced expressions of IL-6, IL-8, p38, p65 and C/EBP-beta were also downregulated by genistein, showing its anti-inflammatory properties. Genistein 111-120 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 19513849-4 2009 Suppression of IL-8 production was blocked by naloxone and naltrindole. Naloxone 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 19513849-4 2009 Suppression of IL-8 production was blocked by naloxone and naltrindole. naltrindole 59-70 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 19407340-4 2009 Herein, we show that lithium induces a rapid and pronounced up-regulation of the matrix metalloproteinase (MMP)-1, an inflammation and senescent cell marker, at the mRNA and protein levels, whereas the induction of two other senescent cell markers is either weak (interleukin-8) or delayed (plasminogen activator inhibitor-1). Lithium 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 264-277 19386603-2 2009 Production of the CXC chemokine interleukin (IL)-8/CXCL8 forms a common epithelial response to many diverse stimuli, including bacterial and viral triggers, environmental oxidants, and other biological mediators, suggesting the potential involvement of a common signaling pathway that may involve DUOX1-dependent H2O2 production. Hydrogen Peroxide 313-317 C-X-C motif chemokine ligand 8 Homo sapiens 51-56 19386603-3 2009 Following previous reports showing that DUOX1 is activated by extracellular ATP and purinergic receptor stimulation, this study demonstrates that airway epithelial IL-8 production in response to several bacterial stimuli involves ATP release and DUOX1 activation. Adenosine Triphosphate 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 19527497-8 2009 The R848-augmented IL-8 release was significantly potentiated by pretreatment with H2O2 (p < 0.01), and N-acetyl-L-cysteine reversed this potentiation. Hydrogen Peroxide 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 19386603-3 2009 Following previous reports showing that DUOX1 is activated by extracellular ATP and purinergic receptor stimulation, this study demonstrates that airway epithelial IL-8 production in response to several bacterial stimuli involves ATP release and DUOX1 activation. Adenosine Triphosphate 230-233 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 19386603-6 2009 Both ADAM17 activation and IL-8 release were suppressed by inhibitors of EGFR/ERK1/2 signaling, which can regulate ADAM17 activity by serine/threonine phosphorylation. Serine 134-140 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 19386603-6 2009 Both ADAM17 activation and IL-8 release were suppressed by inhibitors of EGFR/ERK1/2 signaling, which can regulate ADAM17 activity by serine/threonine phosphorylation. Threonine 141-150 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 19386603-7 2009 Collectively, our results indicate that ATP-mediated DUOX1 activation represents a common response mechanism to several environmental stimuli, involving H2O2-dependent EGFR/ERK activation, ADAM17 activation, and EGFR ligand shedding, leading to amplified epithelial EGFR activation and IL-8 production. Adenosine Triphosphate 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 286-290 19386603-7 2009 Collectively, our results indicate that ATP-mediated DUOX1 activation represents a common response mechanism to several environmental stimuli, involving H2O2-dependent EGFR/ERK activation, ADAM17 activation, and EGFR ligand shedding, leading to amplified epithelial EGFR activation and IL-8 production. Hydrogen Peroxide 153-157 C-X-C motif chemokine ligand 8 Homo sapiens 286-290 19527497-10 2009 The H2O2-potentiated IL-8 release was suppressed by MG-132, a proteosome inhibitor, and by dexamethasone. Hydrogen Peroxide 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 19527497-10 2009 The H2O2-potentiated IL-8 release was suppressed by MG-132, a proteosome inhibitor, and by dexamethasone. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 52-58 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 19527497-10 2009 The H2O2-potentiated IL-8 release was suppressed by MG-132, a proteosome inhibitor, and by dexamethasone. Dexamethasone 91-104 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 19345231-6 2009 The generation of cytokines of significance for adhesive and proliferative events in host defense, IL-8 and G-CSF, was also potently impaired by EtP. ethyl pyruvate 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 19345231-7 2009 SIGNIFICANCE: Exposure of lung epithelial cells to 2.5-10 mM EtP inhibited the generation of inflammatory-regulating cytokines IL-8 and G-CSF, reduced ICAM-1 and VCAM-1 expression and impeded the adhesiveness of neutrophils to lung epithelial cells. ethyl pyruvate 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 19201759-11 2009 Luminal ILT layers displayed potent neutrophil chemotactic activity in vitro, which was inhibited by RANTES- and IL-8-blocking antibodies as well as by reparixin, an antagonist of the IL-8 receptors CXCR1 and CXCR2. reparixin 152-161 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 19349617-0 2009 The 15(S)-hydroxyeicosatetraenoic acid-induced angiogenesis requires Janus kinase 2-signal transducer and activator of transcription-5B-dependent expression of interleukin-8. 15-hydroxy-5,8,11,13-eicosatetraenoic acid 4-38 C-X-C motif chemokine ligand 8 Homo sapiens 160-173 19349617-7 2009 In addition, neutralizing anti-IL-8 antibodies reduced 15(S)-HETE-induced HRMVEC migration and tube formation and Matrigel plug angiogenesis. Hydroxyeicosatetraenoic Acids 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 19483309-6 2009 PMA plus A23187 significantly increased IL-1beta, IL-6, IL-8, and TNF-alpha production compared with media control (p<0.05). Calcimycin 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 19503797-8 2009 AZT pretreatment prevented the up-regulation of some genes, such as MUC5AC and MMP9, triggered by the inflammatory stimulus, but the up-regulation of other inflammatory genes, e.g., cytokines and chemokines, such as interleukin-8, was not affected. Azithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 216-229 19503797-10 2009 Notably, secreted IL-8 protein levels did not reflect mRNA levels, and were, in fact, higher after AZT pretreatment in cultures exposed to the inflammatory stimulus, suggesting that AZT can affect inflammatory pathways other than by altering gene expression. Azithromycin 99-102 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 19503797-10 2009 Notably, secreted IL-8 protein levels did not reflect mRNA levels, and were, in fact, higher after AZT pretreatment in cultures exposed to the inflammatory stimulus, suggesting that AZT can affect inflammatory pathways other than by altering gene expression. Azithromycin 182-185 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 19477431-3 2009 Here, we demonstrate that both IL-8 and angiogenin contribute to the complementary pathways of angiogenesis and BMDC mobilization to increase tumor growth. bmdc 112-116 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 19234105-9 2009 In addition, UFCAP exposure resulted in a significant increase in blood levels of the fibrin degradation product D-dimer as well as a modest elevation in the inflammatory chemokine IL-8 recovered in the lavage fluid. ufcap 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 19357230-0 2009 Lipoxin A4 inhibits IL-1beta-induced IL-8 and ICAM-1 expression in 1321N1 human astrocytoma cells. lipoxin A4 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 19357230-7 2009 As shown by quantitative RT-PCR, LXA(4) (10 nM) significantly inhibited (P < 0.05) the IL-1beta-induced stimulation of IL-8 and ICAM-1 expression in these cells. N-(1H-benzimidazol-2-ylmethyl)-2-methoxyacetamide 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 19357230-8 2009 Furthermore, LXA(4) (10 nM) decreased the expression of IL-1beta-induced IL-8 protein levels (P < 0.05). lipoxin A4 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 19299007-10 2009 The materials may also suppress excessive inflammation by adsorption of the cytokine IL-8 into the porous, internal carbon structure. Carbon 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 19517319-4 2009 In a phase IIa trial in patients with prostatitis, elocalcitol significantly reduced levels of IL-8 in semen, suggesting improved quality and forward motility of sperm. BXL628 51-62 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 19514995-6 2009 MW (1 mg/ml) inhibited PMA plus A23187-stimulated gene expression and production of TNF-alpha, IL-6, and IL-8. Calcimycin 32-38 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 19401270-4 2009 In these studies, the effect of 17beta-estradiol (E(2)) on the expression levels of IL-6, IL-8 and their receptors was investigated. Estradiol 32-48 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 19401270-8 2009 Tamoxifen (Txf), an ER antagonist, completely abolished E(2)-stimulated cell growth and the expression of IL-6 and IL-8. Tamoxifen 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19401270-8 2009 Tamoxifen (Txf), an ER antagonist, completely abolished E(2)-stimulated cell growth and the expression of IL-6 and IL-8. Tamoxifen 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19401270-8 2009 Tamoxifen (Txf), an ER antagonist, completely abolished E(2)-stimulated cell growth and the expression of IL-6 and IL-8. Estradiol 56-60 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19401270-9 2009 IL-6/IL-8-induced cell proliferation was completely blocked by their specific neutralizing antibodies, which partially inhibited E(2)-induced cell growth. Estradiol 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 19398228-7 2009 Silybin (25-50 microM), inhibited the IL-1-induced synthesis of MCP-1 (P < 0.01) and IL-8 (P < 0.01) showing a potent anti-inflammatory activity. Silybin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 19454720-6 2009 Induction of CCL2, CCL7, CXCL3, and CXCL8 by anti-IgE was significantly inhibited by dexamethasone but was enhanced by FK506. Tacrolimus 119-124 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 19454705-5 2009 UDP-glucose stimulated IL-8 production via P2RY14 in human endometrial epithelial cells but not stromal cells. Uridine Diphosphate Glucose 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 19307749-7 2009 The suppressive effect of dexamethasone on TNF-alpha-induced IL-8 transcription was not affected by GRbeta overexpression, rather GRbeta had its own weak suppressive activity on TNF-alpha-induced IL-8 expression. Dexamethasone 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 19454705-6 2009 Furthermore, UDP-glucose enhanced neutrophil chemotaxis in the presence of a human endometrial epithelial cell line in an IL-8-dependent manner. Uridine Diphosphate Glucose 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 19439372-3 2009 Thus, aluminum salts activate dendritic cells, monocytes and macrophages with enhanced expression of adhesion molecules CD54 and CD58 and co-stimulatory molecules CD40 and CD86, which are crucial in T cell activation; induce chemokines CCL2, CCL3, CCL4 and CXCL8, which mediate recruitment of inflammatory cells at the site of vaccination; and stimulate cytokines crucial in the innate immune response. aluminum salts 6-20 C-X-C motif chemokine ligand 8 Homo sapiens 257-262 19454720-6 2009 Induction of CCL2, CCL7, CXCL3, and CXCL8 by anti-IgE was significantly inhibited by dexamethasone but was enhanced by FK506. Dexamethasone 85-98 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 19485829-5 2009 RESULTS: Laser irradiation of LPS-coated titanium disks significantly reduced LPS-induced nitric oxide production and cell activation by the macrophages and strongly attenuated intercellular adhesion molecule-1 and vascular cell adhesion molecule expression, as well as interleukin-8 production by the endothelial cells. Titanium 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 270-283 19185596-9 2009 An NF-kappaB inhibitor, TPCK (N-Tosyl-L-Phenylalanine Chloromethyl Ketone) could suppress IL-8 production and secretion in response to S protein in PBMC and THP-1 cells and in HCoV-229E virus-infected PBMC. Tosylphenylalanyl Chloromethyl Ketone 30-73 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 19470239-0 2009 Inhibitory effects of flavonoids on TNF-alpha-induced IL-8 gene expression in HEK 293 cells. Flavonoids 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 19135038-6 2009 Our results showed that preincubation with 20 microM beta-carotene significantly enhanced the release of two pro-inflammatory mediators, interleukin-8 and tumor necrosis factor-alpha, in PMA-stimulated HL-60 cells and slightly increased the DNA-damaging ability of these cells. beta Carotene 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 137-182 19470239-2 2009 In this study, we demonstrated that several flavonoids, including kaempferol, quercetin, fisetin, and chrysin block TNF-alpha induced IL-8 promoter activation and gene expression in HEK 293 cells. Flavonoids 44-54 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 19470239-2 2009 In this study, we demonstrated that several flavonoids, including kaempferol, quercetin, fisetin, and chrysin block TNF-alpha induced IL-8 promoter activation and gene expression in HEK 293 cells. kaempferol 66-76 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 19470239-2 2009 In this study, we demonstrated that several flavonoids, including kaempferol, quercetin, fisetin, and chrysin block TNF-alpha induced IL-8 promoter activation and gene expression in HEK 293 cells. Quercetin 78-87 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 19470239-2 2009 In this study, we demonstrated that several flavonoids, including kaempferol, quercetin, fisetin, and chrysin block TNF-alpha induced IL-8 promoter activation and gene expression in HEK 293 cells. fisetin 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 19452583-7 2009 HP-NAP could slightly up-regulate IL-8 production in gastric epithelial cell lines but had no effect on GRO(alpha) production. hp-nap 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 19394230-0 2009 6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis. 6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine 0-64 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 19394230-0 2009 6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis. derivatives 76-87 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 19454816-7 2009 RESULTS: A significant effect of the etiology on the levels of IL-8 in the alcohol group as compared to the gallstone group (P=0.003) was found. Alcohols 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 19173296-0 2009 Regulation of deoxycholate induction of CXCL8 by the adenomatous polyposis coli gene in colorectal cancer. Deoxycholic Acid 14-26 C-X-C motif chemokine ligand 8 Homo sapiens 40-45 19173296-3 2009 DCA increased steady state mRNA and protein levels of CXCL8 in cells which do not express wild-type APC. Deoxycholic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 54-59 19173296-4 2009 Steady-state CXCL8 mRNA and protein were suppressed when cells with conditional expression of wild-type APC were exposed to DCA. Deoxycholic Acid 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 13-18 19349368-5 2009 Incubating human microvascular endothelial cells with the sphingosine-1-phosphate type 1 receptor (S1P(1)) inhibitor VPC23019 or performing small interfering RNA knockdown of S1P(1) blocked arsenic-stimulated HMVEC angiogenic gene expression and tube formation, but did not affect induction of either HMOX1 or IL8. Arsenic 190-197 C-X-C motif chemokine ligand 8 Homo sapiens 310-313 19173296-10 2009 Mutation of activator protein-1 (AP-1) or nuclear factor kappa B (NF-kappaB) sites suppressed the activation of the CXCL8 promoter-reporter by DCA. Deoxycholic Acid 143-146 C-X-C motif chemokine ligand 8 Homo sapiens 116-121 19173296-11 2009 Chromatin immunoprecipitation revealed that AP-1 and NF-kappaB binding to the 5"-promoter of CXCL8 was induced by DCA. Deoxycholic Acid 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 19173296-13 2009 Phenotypic assays determined that DCA-mediated invasion was blocked by antibody-directed against CXCL8 or wild-type APC. Deoxycholic Acid 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 97-102 19173296-15 2009 These data suggest that DCA-mediated CXCL8 occurs in initiated colonic epithelium and neutralizing CXCL8 could reduce the invasive potential of tumors. Deoxycholic Acid 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 37-42 19173296-15 2009 These data suggest that DCA-mediated CXCL8 occurs in initiated colonic epithelium and neutralizing CXCL8 could reduce the invasive potential of tumors. Deoxycholic Acid 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 19452017-9 2009 RESULTS: The expressions of MIP1-alpha, MIP1-beta, IL-6, IL-8, RANTES, IFN-beta, and TLR3 were up-regulated in HCECs exposed to poly(I:C). poly 128-132 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 19452017-10 2009 The poly(I:C)-induced expressions of IL-6 and IL-8 were down-regulated by both DEX and CsA, while the expressions of IFN-beta and TLR3 were suppressed by DEX alone. Poly I-C 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19452017-10 2009 The poly(I:C)-induced expressions of IL-6 and IL-8 were down-regulated by both DEX and CsA, while the expressions of IFN-beta and TLR3 were suppressed by DEX alone. Dexamethasone 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19461497-8 2009 Furthermore, eCO levels significantly correlated with BAL neutrophilia and IL-8 levels in the cohort as a whole (r=0.50; P=0.0005 for total cells, r=0.43; P=0.003 for %cells and r=0.30; P=0.045 for IL-8). ECO 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 19461497-8 2009 Furthermore, eCO levels significantly correlated with BAL neutrophilia and IL-8 levels in the cohort as a whole (r=0.50; P=0.0005 for total cells, r=0.43; P=0.003 for %cells and r=0.30; P=0.045 for IL-8). ECO 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 19258275-3 2009 In NHEK, the production of IL-8 stimulated by an agonist peptide of PAR2, SLIGKIV-NH(2), at 100 microM was significantly reduced by TET, DOX, or MIN at 5 and 10 microM, concentrations that are noncytotoxic. tet 132-135 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 19286926-0 2009 alpha,beta-Unsaturated aldehydes contained in cigarette smoke elicit IL-8 release in pulmonary cells through mitogen-activated protein kinases. alpha,beta-unsaturated aldehydes 0-32 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 19286926-3 2009 By examining a panel of 19 cytokines and chemokines, we found that IL-8 release was elevated by CSE as well as by acrolein, whereas other inflammatory mediators were mostly unaffected. Acrolein 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 19286926-4 2009 CSE-evoked IL-8 release was mimicked by acrolein and crotonaldehyde at concentrations (3-60 microM each) found in CSE and fully prevented by 1 mM alpha,beta-unsaturated aldehydes scavengers N-acetylcysteine (NAC) or sodium 2-mercaptoethanesulfonate. Acrolein 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19286926-4 2009 CSE-evoked IL-8 release was mimicked by acrolein and crotonaldehyde at concentrations (3-60 microM each) found in CSE and fully prevented by 1 mM alpha,beta-unsaturated aldehydes scavengers N-acetylcysteine (NAC) or sodium 2-mercaptoethanesulfonate. 2-butenal 53-67 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19286926-4 2009 CSE-evoked IL-8 release was mimicked by acrolein and crotonaldehyde at concentrations (3-60 microM each) found in CSE and fully prevented by 1 mM alpha,beta-unsaturated aldehydes scavengers N-acetylcysteine (NAC) or sodium 2-mercaptoethanesulfonate. alpha,beta-unsaturated aldehydes 146-178 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19286926-4 2009 CSE-evoked IL-8 release was mimicked by acrolein and crotonaldehyde at concentrations (3-60 microM each) found in CSE and fully prevented by 1 mM alpha,beta-unsaturated aldehydes scavengers N-acetylcysteine (NAC) or sodium 2-mercaptoethanesulfonate. Acetylcysteine 190-206 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19286926-4 2009 CSE-evoked IL-8 release was mimicked by acrolein and crotonaldehyde at concentrations (3-60 microM each) found in CSE and fully prevented by 1 mM alpha,beta-unsaturated aldehydes scavengers N-acetylcysteine (NAC) or sodium 2-mercaptoethanesulfonate. Acetylcysteine 208-211 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19286926-4 2009 CSE-evoked IL-8 release was mimicked by acrolein and crotonaldehyde at concentrations (3-60 microM each) found in CSE and fully prevented by 1 mM alpha,beta-unsaturated aldehydes scavengers N-acetylcysteine (NAC) or sodium 2-mercaptoethanesulfonate. Mesna 216-248 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 19286926-6 2009 In addition, CSE or crotonaldehyde upregulated the release of IL-8 from alveolar macrophages from both COPD patients and healthy nonsmokers, indicating that this is a response common to cells involved in lung inflammation. 2-butenal 20-34 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 19286926-10 2009 In summary, our data show that alpha,beta-unsaturated aldehydes-evoked phosphorylation of p38 and ERK1/2 underlies IL-8 release elicited by CSE, thus shedding light on the mechanisms through which cigarette smoke can initiate inflammation in the lung. alpha,beta-unsaturated aldehydes 31-63 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19286927-0 2009 Ceramide-dependent PP2A regulation of TNFalpha-induced IL-8 production in respiratory epithelial cells. Ceramides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 19286927-5 2009 Inhibition of PP2A using okadaic acid or gene knockdown using siRNA resulted in an augmentation of TNFalpha-induced IL-8 production. Okadaic Acid 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 19286927-8 2009 Inhibition of the immediate sphingomyelinase-dependent pathway as well as the de novo synthesis pathway of ceramide production reduced serine/threonine phosphatase activity and augmented IL-8 production. Ceramides 107-115 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 19286927-9 2009 These data suggest that ceramide plays a role in activating PP2A to terminate ongoing IL-8 production. Ceramides 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 19286927-10 2009 In summary, our data suggest that in respiratory epithelium, TNFalpha induces ceramide accumulation, resulting in subsequent activation of PP2A, which targets those kinases responsible for transcriptional activation of IL-8. Ceramides 78-86 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). Tetracycline 42-54 C-X-C motif chemokine ligand 8 Homo sapiens 151-164 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). Tetracycline 42-54 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). tet 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 151-164 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). tet 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). Doxycycline 89-100 C-X-C motif chemokine ligand 8 Homo sapiens 151-164 19258275-3 2009 In NHEK, the production of IL-8 stimulated by an agonist peptide of PAR2, SLIGKIV-NH(2), at 100 microM was significantly reduced by TET, DOX, or MIN at 5 and 10 microM, concentrations that are noncytotoxic. Doxycycline 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). Doxycycline 89-100 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). Doxycycline 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 151-164 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). Doxycycline 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). Minocycline 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 151-164 19258275-2 2009 In this study, we examined the effects of tetracycline (TET) and two of its derivatives, doxycycline (DOX) and minocycline (MIN), on the production of interleukin-8 (IL-8) elicited by the activation of protease-activated receptor 2 (PAR2) in normal human epidermal keratinocytes (NHEK). Minocycline 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 19258275-6 2009 These results suggest that tetracyclines attenuate the PAR2-IL-8 axis in keratinocytes and thereby effectively modulate proinflammatory responses in the skin. Tetracyclines 27-40 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 19362486-2 2009 These compounds were designed as development of previous pyrazole-urea derivatives that resulted potent IL8-induced neutrophil chemotaxis inhibitors in vitro. pyrazole 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 19711862-3 2009 Microgravity effects simulated with the use of RPM raised the IL-8 production 1.5 - 6 times and 1.6-2.1 times on the average after 10 days and 20 days of containment, respectively. Sirolimus 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 19229069-0 2009 Human IL-8 regulates smooth muscle cell VCAM-1 expression in response to endothelial cells exposed to atheroprone flow. atheroprone 102-113 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 19229069-2 2009 Recently, we showed that atheroprone hemodynamics induced IL-8 secretion from endothelial cells (ECs) concurrent with increased EC/smooth muscle cell (SMC) VCAM-1 expression in a human hemodynamic coculture model. atheroprone 25-36 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 19362486-2 2009 These compounds were designed as development of previous pyrazole-urea derivatives that resulted potent IL8-induced neutrophil chemotaxis inhibitors in vitro. Urea 66-70 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 19303321-3 2009 Indeed, the migration of human neutrophils towards IL-8 was significantly inhibited by the P2Y receptor antagonists, suramin and reactive blue 2 (RB-2) and potentiated by a P2Y(2) ligand, ATP, but insensitive to specific antagonists of P2Y(1), P2Y(6) and P2Y(11) receptors. Suramin 117-124 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 19303321-3 2009 Indeed, the migration of human neutrophils towards IL-8 was significantly inhibited by the P2Y receptor antagonists, suramin and reactive blue 2 (RB-2) and potentiated by a P2Y(2) ligand, ATP, but insensitive to specific antagonists of P2Y(1), P2Y(6) and P2Y(11) receptors. Cibacron Blue F 3GA 129-144 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 19303321-3 2009 Indeed, the migration of human neutrophils towards IL-8 was significantly inhibited by the P2Y receptor antagonists, suramin and reactive blue 2 (RB-2) and potentiated by a P2Y(2) ligand, ATP, but insensitive to specific antagonists of P2Y(1), P2Y(6) and P2Y(11) receptors. Adenosine Triphosphate 188-191 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 19085995-6 2009 Data demonstrated that DSS activates IkappaBalpha, NFkappaB, and IL-8 through an ROS-Hsp27-IKKbeta-mediated pathway, and not through an innate immune cascade. Reactive Oxygen Species 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 19303321-5 2009 Taken together, these data suggest that extracellular ATP is necessary for IL-8 to exert its chemotactic effect on neutrophils. Adenosine Triphosphate 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 19285497-0 2009 Sphingosine-1-phosphate increases human alveolar epithelial IL-8 secretion, proliferation and neutrophil chemotaxis. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 19085995-3 2009 METHODS: DSS-induced increases in phospho-IkappaBalpha, nuclear NFkappaB (p65), and IL-8 secretion in human colonic epithelial cells in tissue culture are attributable to a reactive oxygen species (ROS)-induced pathway of inflammation, and do not require TLR4, MyD88, or Bcl10, which are associated with the innate immune pathway of NFkappaB-IL-8 activation. dss 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 19241441-5 2009 Evodiamine and rutaecarpine decreased the LIGHT-induced production of ROS, IL-8, monocyte chemoattractant protein-1 (MCP-1), TNF-alpha, and IL-6, as well as the expression of chemokine receptor (CCR) 1, CCR2 and ICAM-1 and the phosphorylation of the ERK 1/2 and p38 MAPK. evodiamine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 19085995-3 2009 METHODS: DSS-induced increases in phospho-IkappaBalpha, nuclear NFkappaB (p65), and IL-8 secretion in human colonic epithelial cells in tissue culture are attributable to a reactive oxygen species (ROS)-induced pathway of inflammation, and do not require TLR4, MyD88, or Bcl10, which are associated with the innate immune pathway of NFkappaB-IL-8 activation. dss 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 342-346 19085995-3 2009 METHODS: DSS-induced increases in phospho-IkappaBalpha, nuclear NFkappaB (p65), and IL-8 secretion in human colonic epithelial cells in tissue culture are attributable to a reactive oxygen species (ROS)-induced pathway of inflammation, and do not require TLR4, MyD88, or Bcl10, which are associated with the innate immune pathway of NFkappaB-IL-8 activation. Reactive Oxygen Species 173-196 C-X-C motif chemokine ligand 8 Homo sapiens 342-346 19085995-6 2009 Data demonstrated that DSS activates IkappaBalpha, NFkappaB, and IL-8 through an ROS-Hsp27-IKKbeta-mediated pathway, and not through an innate immune cascade. dss 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 19360326-6 2009 Compared to untreated cells, expression of intracellular HO-1-protein and release of IL-8 into cell culture supernatants and corresponding mRNA expression were attenuated in THP-1 cells exposed to sevoflurane and isoflurane, respectively. Sevoflurane 197-208 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 19360326-6 2009 Compared to untreated cells, expression of intracellular HO-1-protein and release of IL-8 into cell culture supernatants and corresponding mRNA expression were attenuated in THP-1 cells exposed to sevoflurane and isoflurane, respectively. Isoflurane 213-223 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 19241441-5 2009 Evodiamine and rutaecarpine decreased the LIGHT-induced production of ROS, IL-8, monocyte chemoattractant protein-1 (MCP-1), TNF-alpha, and IL-6, as well as the expression of chemokine receptor (CCR) 1, CCR2 and ICAM-1 and the phosphorylation of the ERK 1/2 and p38 MAPK. rutecarpine 15-27 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 19085995-0 2009 ROS, Hsp27, and IKKbeta mediate dextran sodium sulfate (DSS) activation of IkappaBa, NFkappaB, and IL-8. Reactive Oxygen Species 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 19085995-0 2009 ROS, Hsp27, and IKKbeta mediate dextran sodium sulfate (DSS) activation of IkappaBa, NFkappaB, and IL-8. dextran sodium sulfate 32-54 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 19085995-0 2009 ROS, Hsp27, and IKKbeta mediate dextran sodium sulfate (DSS) activation of IkappaBa, NFkappaB, and IL-8. dss 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 19434815-0 2009 Treatment with levamisole and colchicine can result in a significant reduction of IL-6, IL-8 or TNF-alpha level in patients with mucocutaneous type of Behcet"s disease. Levamisole 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 19220658-11 2009 In addition, we found muscovite inhibited the expression of TNF-alpha, IL-1beta secreted by THP-1 and IL-8 secreted by HT-29 cells in a dose-dependent manner. muscovite 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 19434815-6 2009 CONCLUSIONS: Treatment with levamisole and colchicine can result in a significant reduction of serum IL-6, IL-8 or TNF-alpha level in MCBD patients. Levamisole 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 19434815-6 2009 CONCLUSIONS: Treatment with levamisole and colchicine can result in a significant reduction of serum IL-6, IL-8 or TNF-alpha level in MCBD patients. Colchicine 43-53 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 19434815-0 2009 Treatment with levamisole and colchicine can result in a significant reduction of IL-6, IL-8 or TNF-alpha level in patients with mucocutaneous type of Behcet"s disease. Colchicine 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 19416633-6 2009 Resveratrol significantly inhibited the PMA plus A23187-induction of inflammatory cytokines such as tumour necrosis factor (TNF)-alpha, interleukin (IL)-6 and IL-8. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 19416633-6 2009 Resveratrol significantly inhibited the PMA plus A23187-induction of inflammatory cytokines such as tumour necrosis factor (TNF)-alpha, interleukin (IL)-6 and IL-8. Tetradecanoylphorbol Acetate 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 21475837-5 2009 PGE2 alone has no effect on IL-8 production, but in cells pretreated with IL-1beta it markedly enhances IL-8 production. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 21475837-6 2009 Moreover, a stimulatory effect of PGE2 on IL-8 production in the synoviocyte MH7A cells was observed. Dinoprostone 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 21475837-7 2009 These results indicate that, in the synovial tissues of patients with rheumatoid arthritis, PGE2 stimulates the release of IL-8 from the fibroblastic cells classified as present, thereby exacerbating inflammation. Dinoprostone 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 19416633-6 2009 Resveratrol significantly inhibited the PMA plus A23187-induction of inflammatory cytokines such as tumour necrosis factor (TNF)-alpha, interleukin (IL)-6 and IL-8. Calcimycin 49-55 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 19175556-6 2009 Despite similar pulmonary function and histologic markers of injury in both groups and higher IL-1beta in the donor of ACDD, IL-8 during reperfusion was significantly lower in ACDD (119 +/- 33% of basal) than in HBD (306 +/- 238%, P < 0.05) recipients. acdd 176-180 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 19416633-10 2009 Resveratrol suppressed the expression of TNF-alpha, IL-6, IL-8 and COX-2 through a decrease in the intracellular levels of Ca2+ and ERK 1/2, as well as activation of NF-kappaB. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 19158122-8 2009 The addition of low-dose theophylline increased HDAC activity and further reduced IL8 and TNFalpha concentrations. Theophylline 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 19103478-9 2009 We suggest that HM can modulate the inflammatory response by inducing IL-8 and IL-6 production via TLR4-dependent activation of the NF-kappaB signaling pathway. His-Met 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 19324137-7 2009 The IL-6 and IL-8 levels were lower in the GAE group (ratio 0.83, 95% confidence interval: 0.68 to 1.02; p = 0.070) than in the GA group (ratio 0.90, 95% confidence interval: 0.78 to 1.02; p = 0.090). gae 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19563733-5 2009 Furthermore, TNF-alpha-induced MCP-1 and IL-8 mRNA expression levels were also attenuated by pretreatment with EZS. 1-[1-(4-fluorobenzyl)-2-methyl-1H-imidazol-4-yl]-1-ethanone 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 19355766-1 2009 Here we report on the polarization dependent nonresonant second harmonic generation (SHG) measurement of the interfacial water molecules at the aqueous solution of the following salts: NaF, NaCl, NaBr, KF, KCl, and KBr. Water 121-126 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 19355766-4 2009 Noticeably, both the cations and the anions contributed to the changes, and the abilities to increase the thickness of the interfacial water layer were in the following order: KBr > NaBr > KCl > NaCl approximately NaF > KF. Water 135-140 C-X-C motif chemokine ligand 8 Homo sapiens 223-226 19355766-4 2009 Noticeably, both the cations and the anions contributed to the changes, and the abilities to increase the thickness of the interfacial water layer were in the following order: KBr > NaBr > KCl > NaCl approximately NaF > KF. Potassium Chloride 195-198 C-X-C motif chemokine ligand 8 Homo sapiens 223-226 19355767-1 2009 Sum frequency generation vibrational spectra of the water molecules at the NaF and KF aqueous solution surfaces showed significantly different spectral features and different concentration dependence. Water 52-57 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 18317936-0 2009 7beta-Hydroxycholesterol and 25-hydroxycholesterol-induced interleukin-8 secretion involves a calcium-dependent activation of c-fos via the ERK1/2 signaling pathway in THP-1 cells: oxysterols-induced IL-8 secretion is calcium-dependent. cholest-5-en-3 beta,7 alpha-diol 0-24 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 18317936-0 2009 7beta-Hydroxycholesterol and 25-hydroxycholesterol-induced interleukin-8 secretion involves a calcium-dependent activation of c-fos via the ERK1/2 signaling pathway in THP-1 cells: oxysterols-induced IL-8 secretion is calcium-dependent. cholest-5-en-3 beta,7 alpha-diol 0-24 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 18317936-8 2009 These results demonstrate that oxysterol-induced IL-8 secretion is a calcium-dependent phenomenon involving the MEK/ERK1/2 pathway leading to the activation of IL-8 gene via AP-1 (c-fos). Oxysterols 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 18317936-0 2009 7beta-Hydroxycholesterol and 25-hydroxycholesterol-induced interleukin-8 secretion involves a calcium-dependent activation of c-fos via the ERK1/2 signaling pathway in THP-1 cells: oxysterols-induced IL-8 secretion is calcium-dependent. 25-hydroxycholesterol 29-50 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 18317936-8 2009 These results demonstrate that oxysterol-induced IL-8 secretion is a calcium-dependent phenomenon involving the MEK/ERK1/2 pathway leading to the activation of IL-8 gene via AP-1 (c-fos). Calcium 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 18317936-0 2009 7beta-Hydroxycholesterol and 25-hydroxycholesterol-induced interleukin-8 secretion involves a calcium-dependent activation of c-fos via the ERK1/2 signaling pathway in THP-1 cells: oxysterols-induced IL-8 secretion is calcium-dependent. 25-hydroxycholesterol 29-50 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 18317936-8 2009 These results demonstrate that oxysterol-induced IL-8 secretion is a calcium-dependent phenomenon involving the MEK/ERK1/2 pathway leading to the activation of IL-8 gene via AP-1 (c-fos). Calcium 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 18317936-0 2009 7beta-Hydroxycholesterol and 25-hydroxycholesterol-induced interleukin-8 secretion involves a calcium-dependent activation of c-fos via the ERK1/2 signaling pathway in THP-1 cells: oxysterols-induced IL-8 secretion is calcium-dependent. Calcium 94-101 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 18317936-0 2009 7beta-Hydroxycholesterol and 25-hydroxycholesterol-induced interleukin-8 secretion involves a calcium-dependent activation of c-fos via the ERK1/2 signaling pathway in THP-1 cells: oxysterols-induced IL-8 secretion is calcium-dependent. Calcium 94-101 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 18317936-0 2009 7beta-Hydroxycholesterol and 25-hydroxycholesterol-induced interleukin-8 secretion involves a calcium-dependent activation of c-fos via the ERK1/2 signaling pathway in THP-1 cells: oxysterols-induced IL-8 secretion is calcium-dependent. Calcium 218-225 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 18317936-2 2009 An oxysterol-induced interleukin-8 (IL-8) secretion in human monocytes/macrophages has been previously noticed, but the mechanisms remained unclear. Oxysterols 3-12 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 18317936-2 2009 An oxysterol-induced interleukin-8 (IL-8) secretion in human monocytes/macrophages has been previously noticed, but the mechanisms remained unclear. Oxysterols 3-12 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 18317936-3 2009 In this paper, we investigated the signaling pathways leading to the induction of IL-8 secretion in monocytic THP-1 cells treated with 7beta-hydroxycholesterol, a cytototoxic oxysterol, or with 25-hydroxycholesterol, an oxysterol non-cytotoxic toward this cell line. cholest-5-en-3 beta,7 alpha-diol 135-159 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 18317936-3 2009 In this paper, we investigated the signaling pathways leading to the induction of IL-8 secretion in monocytic THP-1 cells treated with 7beta-hydroxycholesterol, a cytototoxic oxysterol, or with 25-hydroxycholesterol, an oxysterol non-cytotoxic toward this cell line. Oxysterols 175-184 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 19076731-7 2009 Clarithromycin reduced the lavage fluid levels of IL-8 at the low-dose histamine observation (P<0.001). Clarithromycin 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 18317936-3 2009 In this paper, we investigated the signaling pathways leading to the induction of IL-8 secretion in monocytic THP-1 cells treated with 7beta-hydroxycholesterol, a cytototoxic oxysterol, or with 25-hydroxycholesterol, an oxysterol non-cytotoxic toward this cell line. 25-hydroxycholesterol 194-215 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 19076731-7 2009 Clarithromycin reduced the lavage fluid levels of IL-8 at the low-dose histamine observation (P<0.001). Histamine 71-80 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 18317936-3 2009 In this paper, we investigated the signaling pathways leading to the induction of IL-8 secretion in monocytic THP-1 cells treated with 7beta-hydroxycholesterol, a cytototoxic oxysterol, or with 25-hydroxycholesterol, an oxysterol non-cytotoxic toward this cell line. Oxysterols 220-229 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 18317936-4 2009 The oxysterol-induced IL-8 secretion appears to be a calcium-dependent phenomenon as shown by the use of calcium channel blockers, which strongly decreased IL-8 secretion and IL-8 messenger RNA (mRNA) levels. Oxysterols 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 18317936-4 2009 The oxysterol-induced IL-8 secretion appears to be a calcium-dependent phenomenon as shown by the use of calcium channel blockers, which strongly decreased IL-8 secretion and IL-8 messenger RNA (mRNA) levels. Oxysterols 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 18317936-4 2009 The oxysterol-induced IL-8 secretion appears to be a calcium-dependent phenomenon as shown by the use of calcium channel blockers, which strongly decreased IL-8 secretion and IL-8 messenger RNA (mRNA) levels. Oxysterols 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 18317936-4 2009 The oxysterol-induced IL-8 secretion appears to be a calcium-dependent phenomenon as shown by the use of calcium channel blockers, which strongly decreased IL-8 secretion and IL-8 messenger RNA (mRNA) levels. Calcium 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 18317936-4 2009 The oxysterol-induced IL-8 secretion appears to be a calcium-dependent phenomenon as shown by the use of calcium channel blockers, which strongly decreased IL-8 secretion and IL-8 messenger RNA (mRNA) levels. Calcium 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 18317936-4 2009 The oxysterol-induced IL-8 secretion appears to be a calcium-dependent phenomenon as shown by the use of calcium channel blockers, which strongly decreased IL-8 secretion and IL-8 messenger RNA (mRNA) levels. Calcium 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 18317936-8 2009 These results demonstrate that oxysterol-induced IL-8 secretion is a calcium-dependent phenomenon involving the MEK/ERK1/2 pathway leading to the activation of IL-8 gene via AP-1 (c-fos). Oxysterols 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 19089992-10 2009 Both 10% and 12% strain levels caused an increase in IL-8 production by hMSCs that was dependent on the presence of dexamethasone. Dexamethasone 116-129 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 19232500-2 2009 Circulating IL-8 is comprised of an endothelial-derived [ala-IL-8](77) isoform and another, more potent [ser-IL-8](72) secreted by most other cells; [ala-IL-8](77) can be converted into [ser-IL-8](72) by proteolytic removal of an N-terminal pentapeptide from [ala-IL-8](77). Serine 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 19232500-2 2009 Circulating IL-8 is comprised of an endothelial-derived [ala-IL-8](77) isoform and another, more potent [ser-IL-8](72) secreted by most other cells; [ala-IL-8](77) can be converted into [ser-IL-8](72) by proteolytic removal of an N-terminal pentapeptide from [ala-IL-8](77). Serine 187-190 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 19232500-3 2009 In this study, we show [ala-IL-8](77) is the predominant circulating isoform of IL-8 in premature neonates but not in term neonates/adults, who have [ser-IL-8](72) as the major isoform. Alanine 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 19159427-6 2009 The adhesin could also induce interleukin-8 secretion from INT-407 cells, which was inhibited in the presence of dantrolene as well as staurosporin (inhibitor of PKC). Dantrolene 113-123 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 19159427-6 2009 The adhesin could also induce interleukin-8 secretion from INT-407 cells, which was inhibited in the presence of dantrolene as well as staurosporin (inhibitor of PKC). Staurosporine 135-147 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 19373630-0 2009 Asthma drugs counter-regulate interleukin-8 release stimulated by sodium sulfite in an A549 cell line. sodium sulfite 66-80 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 19373630-6 2009 To date, there have not been any reports on the effect of asthma drugs on the suppression of IL-8 production induced by sulfite in A549 cells or the involvement of specific signal transduction pathways. Sulfites 120-127 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 19373630-10 2009 RESULTS: IL-8 production increased after treatment with sodium sulfite at 1000 to 2500 uM (p <or= 0.001). sodium sulfite 56-70 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 19373630-11 2009 SB203580, PD98059, and wedeloactone decreased IL-8 production stimulated by Na(2)SO(3) (p < 0.01). SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19373630-11 2009 SB203580, PD98059, and wedeloactone decreased IL-8 production stimulated by Na(2)SO(3) (p < 0.01). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19232500-3 2009 In this study, we show [ala-IL-8](77) is the predominant circulating isoform of IL-8 in premature neonates but not in term neonates/adults, who have [ser-IL-8](72) as the major isoform. Alanine 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 19232500-3 2009 In this study, we show [ala-IL-8](77) is the predominant circulating isoform of IL-8 in premature neonates but not in term neonates/adults, who have [ser-IL-8](72) as the major isoform. Alanine 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 19232500-4 2009 This isoform switch from the less potent [ala-IL-8](77) to [ser-IL-8](72) correlates with a maturational increase in the neutrophil chemotactic potency of plasma IL-8. Alanine 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19232500-4 2009 This isoform switch from the less potent [ala-IL-8](77) to [ser-IL-8](72) correlates with a maturational increase in the neutrophil chemotactic potency of plasma IL-8. Alanine 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 19232500-4 2009 This isoform switch from the less potent [ala-IL-8](77) to [ser-IL-8](72) correlates with a maturational increase in the neutrophil chemotactic potency of plasma IL-8. Alanine 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 19232500-4 2009 This isoform switch from the less potent [ala-IL-8](77) to [ser-IL-8](72) correlates with a maturational increase in the neutrophil chemotactic potency of plasma IL-8. Serine 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19232500-4 2009 This isoform switch from the less potent [ala-IL-8](77) to [ser-IL-8](72) correlates with a maturational increase in the neutrophil chemotactic potency of plasma IL-8. Serine 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 19232500-4 2009 This isoform switch from the less potent [ala-IL-8](77) to [ser-IL-8](72) correlates with a maturational increase in the neutrophil chemotactic potency of plasma IL-8. Serine 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 19232500-5 2009 The emergence of [ser-IL-8](72) as the major isoform is likely due to increased plasma [ala-IL-8](77)-convertase activity and/or changes in the cellular sources of IL-8. Serine 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 19232500-5 2009 The emergence of [ser-IL-8](72) as the major isoform is likely due to increased plasma [ala-IL-8](77)-convertase activity and/or changes in the cellular sources of IL-8. Serine 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 19232500-5 2009 The emergence of [ser-IL-8](72) as the major isoform is likely due to increased plasma [ala-IL-8](77)-convertase activity and/or changes in the cellular sources of IL-8. Serine 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 18759324-8 2009 BaAlFSi particles induced a more marked IL-8 response compared to BaAlSi particles, whereas no significant difference was observed for the IL-6 response. baalfsi 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 19373630-11 2009 SB203580, PD98059, and wedeloactone decreased IL-8 production stimulated by Na(2)SO(3) (p < 0.01). wedeloactone 23-35 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19373630-11 2009 SB203580, PD98059, and wedeloactone decreased IL-8 production stimulated by Na(2)SO(3) (p < 0.01). sodium sulfite 76-86 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 19373630-12 2009 Salmeterol, fluticasone, and montelukast significantly suppressed IL-8 secretion from sodium sulfite-stimulated A549 cells (p < 0.01). Salmeterol Xinafoate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 19373630-12 2009 Salmeterol, fluticasone, and montelukast significantly suppressed IL-8 secretion from sodium sulfite-stimulated A549 cells (p < 0.01). Fluticasone 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 19129482-8 2009 Priming with the allergic mediators histamine, IL-4, and most prominently IL-5, augmented the TLR-induced IL-8 and EDN secretion, revealing an ability to sensitize eosinophils for TLR7 and TLR9 activation. Histamine 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 19373630-12 2009 Salmeterol, fluticasone, and montelukast significantly suppressed IL-8 secretion from sodium sulfite-stimulated A549 cells (p < 0.01). montelukast 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 19373630-12 2009 Salmeterol, fluticasone, and montelukast significantly suppressed IL-8 secretion from sodium sulfite-stimulated A549 cells (p < 0.01). sodium sulfite 86-100 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 19373630-13 2009 CONCLUSIONS: Sodium sulfite has pro-inflammatory properties in vitro and can induce potent chemotactic factor IL-8 production. sodium sulfite 13-27 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 19373630-15 2009 Salmeterol, fluticasone, and montelukast all have inhibitory effects on sodium sulfite-induced IL-8 production in A549 cells. Salmeterol Xinafoate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 19373630-15 2009 Salmeterol, fluticasone, and montelukast all have inhibitory effects on sodium sulfite-induced IL-8 production in A549 cells. Fluticasone 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 19373630-15 2009 Salmeterol, fluticasone, and montelukast all have inhibitory effects on sodium sulfite-induced IL-8 production in A549 cells. montelukast 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 19373630-15 2009 Salmeterol, fluticasone, and montelukast all have inhibitory effects on sodium sulfite-induced IL-8 production in A549 cells. sodium sulfite 72-86 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 19299743-7 2009 Together, IL-8 and PGP account for most of the neutrophil chemoattractant capacity seen in BOS BAL fluid. N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 19299743-8 2009 Using specific neutralizing Abs to both IL-8 and PGP, we demonstrate that PGP is a prominent neutrophil chemoattractant found in BAL fluid from individuals at the time of diagnosis of BOS. pgp 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 19345795-0 2009 Prostaglandin F(2alpha)-induced interleukin-8 production in human dental pulp cells is associated with MEK/ERK signaling. Prostaglandins F 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 19345795-4 2009 IL-1beta and PGF(2alpha) (0.5-10 mumol/L) also induced IL-8 production and mRNA expression in pulp cells. Prostaglandins F 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 19345795-6 2009 PGF(2alpha)-induced IL-8 production and mRNA expression were inhibited by U0126 (an inhibitor of mitogen-activated protein kinase kinase [MEK1/2]) inhibitor), whereas SQ22536 (an adenylate cyclase inhibitor) enhanced this event. Prostaglandins F 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 19345795-6 2009 PGF(2alpha)-induced IL-8 production and mRNA expression were inhibited by U0126 (an inhibitor of mitogen-activated protein kinase kinase [MEK1/2]) inhibitor), whereas SQ22536 (an adenylate cyclase inhibitor) enhanced this event. U 0126 74-79 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 19345795-8 2009 PGF(2alpha)-induced IL-8 production is possibly via activation of MEK/extracellular signal-regulated kinase signaling, but not by activation of adenylate cyclase. Prostaglandins F 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 19345795-9 2009 IL-1beta and PGF(2alpha) might involve the pathogenesis of pulpal inflammation via induction of IL-8 production. Prostaglandins F 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 19216880-5 2009 Although the presence of Cu(2+), Co(2+) and Fe(3+) decreased the fluorescence intensity of DBHQ-Ga(3+), the addition of a fluoride ion (NaF) recovered the fluorescence by masking the interfering ions. dbhq-ga 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 19107880-0 2009 The vitamin D receptor agonist elocalcitol inhibits IL-8-dependent benign prostatic hyperplasia stromal cell proliferation and inflammatory response by targeting the RhoA/Rho kinase and NF-kappaB pathways. BXL628 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 19107880-7 2009 RESULTS: Stimulation of BPH cells with IL-8 activates the calcium-sensitizing RhoA/ROCK pathway, as demonstrated by the increased membrane translocation of RhoA and by phosphorylation of the ROCK substrate myosin phosphatase target subunit 1 (MYPT-1). Calcium 58-65 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 19107880-9 2009 The VDR agonist elocalcitol significantly inhibits IL-8 production by BPH cells stimulated with inflammatory cytokines, and IL-8-induced proliferation of BPH cells. BXL628 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 19107880-10 2009 In addition, elocalcitol inhibits IL-8-induced membrane translocation of RhoA and MYPT-1 phosphorylation in BPH cells, and inhibits dose-dependently their IL-8-dependent invasion. BXL628 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 19107880-10 2009 In addition, elocalcitol inhibits IL-8-induced membrane translocation of RhoA and MYPT-1 phosphorylation in BPH cells, and inhibits dose-dependently their IL-8-dependent invasion. BXL628 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 19107880-11 2009 The inhibition induced by elocalcitol of IL-8 production by BPH cells is accompanied by decreased COX-2 expression and PGE(2) production and by arrest of NF-kappaB p65 nuclear translocation, associated with inhibition of the RhoA/ROCK pathway. BXL628 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 19107880-11 2009 The inhibition induced by elocalcitol of IL-8 production by BPH cells is accompanied by decreased COX-2 expression and PGE(2) production and by arrest of NF-kappaB p65 nuclear translocation, associated with inhibition of the RhoA/ROCK pathway. Dinoprostone 119-125 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 21136970-6 2009 Our secretome-based proteomic studies have identified several secreted modulators of sulindac-induced apoptosis action (e.g., Mac-2 binding protein, Alix, 14-3-3 isoforms, profilin-1, calumenin/Cab45 precursors, and the angiogenic/tumor growth factors interleukin 8 (IL-8) and growth related oncogene (GRO-alpha)) that are likely to improve our understanding of the chemopreventitive action of this NSAID in CRC. Sulindac 85-93 C-X-C motif chemokine ligand 8 Homo sapiens 252-265 19216880-5 2009 Although the presence of Cu(2+), Co(2+) and Fe(3+) decreased the fluorescence intensity of DBHQ-Ga(3+), the addition of a fluoride ion (NaF) recovered the fluorescence by masking the interfering ions. Fluorides 122-130 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 19135383-5 2009 We also found that IL-1beta-induced release of IL-8 from MH7A cells was completely blocked by pretreatment with the (IL-8) inhibitor Bay11-7085, indicating that activation of NF-kappaB signaling plays an important role in the secretion of IL-8. BAY 11-7085 133-143 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 19038492-2 2009 Recent reports show that phosphorylation of p65 at serine 276 regulates only a subset of genes, such as those encoding IL-6, IL-8, Gro-beta, and ICAM-1. Serine 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 19135383-4 2009 We found that LPIL exerted a smaller effect on gene transcription than Dex; however, IL-1beta-inducible target genes such as the CXCL type chemokines IL-8, IL-1beta and IL-6 were all clearly suppressed by LPIL to the same degree as by Dex. lpil 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 19135383-5 2009 We also found that IL-1beta-induced release of IL-8 from MH7A cells was completely blocked by pretreatment with the (IL-8) inhibitor Bay11-7085, indicating that activation of NF-kappaB signaling plays an important role in the secretion of IL-8. BAY 11-7085 133-143 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 19135383-5 2009 We also found that IL-1beta-induced release of IL-8 from MH7A cells was completely blocked by pretreatment with the (IL-8) inhibitor Bay11-7085, indicating that activation of NF-kappaB signaling plays an important role in the secretion of IL-8. BAY 11-7085 133-143 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 19135383-7 2009 Thus LPIL likely exerts its anti-inflammatory effects by inhibiting the release of the inflammatory chemokine IL-8. lpil 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 18758684-5 2009 The level of VEGF, IL-8 and Angiogenin were increased in pioglitazone than rosiglitazone group. Pioglitazone 57-69 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 19247018-11 2009 The EPA group had a significantly (P < 0.05) attenuated stress response for TNFalpha, IL-10, and IL-8 compared with the standard group. Eicosapentaenoic Acid 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 19120068-11 2009 Airway cells that were primed with alcohol produced nearly twice as much IL-8 in response to 40 ng of peptidoglycan than naive cells. Alcohols 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 19112099-9 2009 The mRNA levels of the proinflammatory cytokines interleukin (IL)-1beta and IL-8 were also lower (P < 0.05) in ethanol-exposed fetuses compared with controls. Ethanol 114-121 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 19112101-0 2009 Role of acylglycerol kinase in LPA-induced IL-8 secretion and transactivation of epidermal growth factor-receptor in human bronchial epithelial cells. lysophosphatidic acid 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 19112101-5 2009 Overexpression of lentiviral AGK wild type increased intracellular LPA production ( approximately 1.8-fold), enhanced LPA-mediated IL-8 secretion, and stimulated tyrosine phosphorylation epidermal growth factor-receptor (EGF-R). lysophosphatidic acid 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 19112101-6 2009 Furthermore, downregulation of native AGK by AGK small interfering RNA decreased intracellular LPA levels ( approximately 2-fold) and attenuated LPA-induced p38 MAPK, JNK, and NF-kappaB activation, tyrosine phosphorylation of EGF-R, and IL-8 secretion. lysophosphatidic acid 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 237-241 19112101-7 2009 These results suggest that native AGK regulates LPA-mediated IL-8 secretion involving MAPKs, NF-kappaB, and transactivation of EGF-R. lysophosphatidic acid 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 19220840-4 2009 BFT-activated nuclear factor-kappaB (NF-kappaB) signals in HT-29 cells and pretreatment with eupatilin suppressed NF-kappaB activation that resulted in the significant inhibition of IL-8 and cyclo-oxygenase-2 expression. eupatilin 93-102 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 19016779-0 2009 Staphylococcus epidermidis polysaccharide intercellular adhesin induces IL-8 expression in human astrocytes via a mechanism involving TLR2. Polysaccharides 27-41 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 19338650-12 2009 The average IL-8 induction was 1330 pg/mL for dupA-positive isolates and 1378 pg/mL for dupA-negative isolates. DUPA 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 19338650-12 2009 The average IL-8 induction was 1330 pg/mL for dupA-positive isolates and 1378 pg/mL for dupA-negative isolates. DUPA 88-92 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 19385035-3 2009 The present study was undertaken using the established co-culture system of Caco-2 epithelial cells with lymphocytes of Peyer"s patch to investigate the expression of IL-8 and IL-6 cytokines and cytokine receptors in the co-culture system after challenge with Shigella F2a-12 lipopolysaccharide (LPS). 12 lipopolysaccharide 273-294 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 19220840-7 2009 In addition, herbimycin A, a specific inhibitor of heat shock protein 90 (Hsp90), decreased the BFT-induced activation of IKK and NF-kappaB, suggesting that Hsp90 is associated with a pathway of IKK-NF-kappaB-IL-8/cyclo-oxygenase-2 gene signalling. herbimycin 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 19029040-12 2009 CONCLUSIONS: ATPgammaS, UTP, and UDP stimulate both basal and TNFalpha-induced IL-8 secretion in RPE cells through an ERK 1/2-dependent pathway. Uridine Diphosphate 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 19212662-9 2009 Moreover, remarkable increases in G-CSF and IL-8 secretions by 8-Br-cAMP-stimulated ESCs during decidualization were completely inhibited by cotreatment with danazol. 8-Bromo Cyclic Adenosine Monophosphate 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 19212662-9 2009 Moreover, remarkable increases in G-CSF and IL-8 secretions by 8-Br-cAMP-stimulated ESCs during decidualization were completely inhibited by cotreatment with danazol. Danazol 158-165 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 19279966-1 2009 AIM: To compare the plaque inhibition efficacy of a sodium fluoride/potassium nitrate (NaF/KNO3 with 1450 ppm F) test dentifrice to a 0.454% stannous fluoride/sodium hexametaphosphate/sodium fluoride positive control dentifrice (SnF2/SHMP with 1450 ppm F). Sodium Fluoride 52-67 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 19029040-2 2009 This investigation focused on whether extracellular nucleotides could contribute to this activation, and the effects of ATPgammaS, UTP, and UDP on the production of IL-8 by RPE cells was studied in relation to their expression of functional P2Y receptors. adenosine 5'-O-(3-thiotriphosphate) 120-129 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 19029040-2 2009 This investigation focused on whether extracellular nucleotides could contribute to this activation, and the effects of ATPgammaS, UTP, and UDP on the production of IL-8 by RPE cells was studied in relation to their expression of functional P2Y receptors. Uridine Triphosphate 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 19029040-2 2009 This investigation focused on whether extracellular nucleotides could contribute to this activation, and the effects of ATPgammaS, UTP, and UDP on the production of IL-8 by RPE cells was studied in relation to their expression of functional P2Y receptors. Uridine Diphosphate 140-143 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 19029040-7 2009 RESULTS: Stimulation of ARPE-19 cells with ATPgammaS, UTP, and UDP induced IL-8 gene transcription and protein secretion. Uridine Triphosphate 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 19029040-7 2009 RESULTS: Stimulation of ARPE-19 cells with ATPgammaS, UTP, and UDP induced IL-8 gene transcription and protein secretion. Uridine Diphosphate 63-66 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 19029040-8 2009 TNFalpha induction of IL-8 secretion was also increased by ATPgammaS, UTP, and UDP. adenosine 5'-O-(3-thiotriphosphate) 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 19029040-8 2009 TNFalpha induction of IL-8 secretion was also increased by ATPgammaS, UTP, and UDP. Uridine Triphosphate 70-73 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 19029040-8 2009 TNFalpha induction of IL-8 secretion was also increased by ATPgammaS, UTP, and UDP. Uridine Diphosphate 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 19029040-9 2009 Nucleotide induction of IL-8 production was blocked by PD98059, and all nucleotides stimulated ERK 1/2 phosphorylation. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 55-62 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 19029040-12 2009 CONCLUSIONS: ATPgammaS, UTP, and UDP stimulate both basal and TNFalpha-induced IL-8 secretion in RPE cells through an ERK 1/2-dependent pathway. adenosine 5'-O-(3-thiotriphosphate) 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 19029040-12 2009 CONCLUSIONS: ATPgammaS, UTP, and UDP stimulate both basal and TNFalpha-induced IL-8 secretion in RPE cells through an ERK 1/2-dependent pathway. Uridine Triphosphate 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 18685861-5 2009 Systolic blood pressure was markedly increased and circulating levels of IL-1beta, IL-1Ra, and IL-8 were significantly reduced during a 2-h interval of PMX. (+)-xylariamide A 152-155 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 19052917-8 2009 We found that the incorporation of the detergent solubilized CXCR1 into phospholipid vesicles in the presence of Gi/Go proteins is required for the reconstitution of (125)I-IL-8 binding. Phospholipids 72-84 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 19010653-9 2009 Quercetin significantly decreased ex vivo LPS-induced TNFalpha- and IL-8 production in a concentration-dependent manner in both groups. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 19103208-5 2009 The STAT1 inhibitor, fludarabine, prevented gp120-induced IL-6 and IL-8 secretion. fludarabine 21-32 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 19103208-6 2009 Inhibitors of STAT1, mitogen activated protein kinase kinase (MEK) (PD98059), and phosphatidyl inositol 3 kinase (PI3K) (LY294002), blocked gp120-induced STAT1 activation and significantly diminished IL-8-, IL-6-, and gp120-induced monocyte adhesion and migration across in vitro BBB models. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 19179025-9 2009 Serum concentrations of IL-8, IL-10, macrophage inflammatory protein (MIP)-1beta and monocyte chemoattractant protein-1 in women treated with paroxetine decreased significantly. Paroxetine 142-152 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 19328934-7 2009 CONCLUSION: Systemic inflammation and IL-8-mediated neutrophilic airway inflammation seem to be associated after LTx. Leukotriene C4 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 19146941-5 2009 RESULTS: HaCaT cells induced the pro-inflammatory cytokines, interleukin-8 (IL-8) and/or interleukin-6 (IL-6) expressions after treatment with polyI:C or PGN. Poly I-C 143-150 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 19146941-5 2009 RESULTS: HaCaT cells induced the pro-inflammatory cytokines, interleukin-8 (IL-8) and/or interleukin-6 (IL-6) expressions after treatment with polyI:C or PGN. Poly I-C 143-150 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 19138665-5 2009 In terms of its functional aspect, we observed that alpha-iso-cubebene strongly stimulated CXCL8 production in human neutrophils. alpha-iso-cubebene 52-70 C-X-C motif chemokine ligand 8 Homo sapiens 91-96 19138665-6 2009 Also, alpha-iso-cubebene-induced CXCL8 production was almost completely inhibited by the calcium chelator, EGTA, thus highlighting the role of calcium signaling in the process. alpha-iso-cubebene 6-24 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 19138665-6 2009 Also, alpha-iso-cubebene-induced CXCL8 production was almost completely inhibited by the calcium chelator, EGTA, thus highlighting the role of calcium signaling in the process. Calcium 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 19179025-12 2009 The action of paroxetine may also be associated with decreases in IL-8, IL-10, MIP-1beta. Paroxetine 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 19138665-6 2009 Also, alpha-iso-cubebene-induced CXCL8 production was almost completely inhibited by the calcium chelator, EGTA, thus highlighting the role of calcium signaling in the process. Egtazic Acid 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 19138665-6 2009 Also, alpha-iso-cubebene-induced CXCL8 production was almost completely inhibited by the calcium chelator, EGTA, thus highlighting the role of calcium signaling in the process. Calcium 143-150 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 19121628-0 2009 ROS and NF-kappaB are involved in upregulation of IL-8 in A549 cells exposed to multi-walled carbon nanotubes. Reactive Oxygen Species 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 19138665-7 2009 Taken together, our results demonstrate that alpha-iso-cubebene is a novel natural compound which stimulates intracellular calcium signaling and CXCL8 production. alpha-iso-cubebene 45-63 C-X-C motif chemokine ligand 8 Homo sapiens 145-150 19011150-7 2009 MEASUREMENTS AND MAIN RESULTS: Oxidants evoked the release of CXCL8 from monocytes/macrophages; this was abrogated by pretreatment with N-acetylcysteine or binding antibodies to TLR2 and was associated with the rapid phosphorylation of IL-1 receptor-associated kinase 1. Acetylcysteine 136-152 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 19121628-0 2009 ROS and NF-kappaB are involved in upregulation of IL-8 in A549 cells exposed to multi-walled carbon nanotubes. Carbon 93-99 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 19221248-8 2009 RESULTS: Curcumin treatment resulted in dose-dependent inhibition of IL-6 and IL-8 in all cell lines. Curcumin 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 19143560-10 2009 With sodium fluoride (NaF) as the subphase electrolyte, it is demonstrated that sodium exhibits a weak complexation-type interaction with the zwitterionic lipids. Sodium Fluoride 5-20 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 19143560-10 2009 With sodium fluoride (NaF) as the subphase electrolyte, it is demonstrated that sodium exhibits a weak complexation-type interaction with the zwitterionic lipids. Sodium 5-11 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 19143561-7 2009 In the present paper, we first prove that the experimental results for sodium fluoride (NaF) can be fitted by a model that is based on simultaneous complexation of sodium ions with up to three lipid molecules, as suggested by recent molecular dynamics simulations. Sodium Fluoride 71-86 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 19143561-7 2009 In the present paper, we first prove that the experimental results for sodium fluoride (NaF) can be fitted by a model that is based on simultaneous complexation of sodium ions with up to three lipid molecules, as suggested by recent molecular dynamics simulations. Sodium 71-77 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 19074641-6 2009 Curcumin, as well as inhibitors of NF-kappaB (SN-50), PKC (chelerythrine), and p44/42 MAPK (PD-098059) abolished the acid-induced expression of IL-6 and IL-8. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 19074641-7 2009 The JNK inhibitor SP-600125 blocked expression/secretion of IL-6 but only partially attenuated IL-8 expression. pyrazolanthrone 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 19074641-8 2009 The p38 MAPK inhibitor SB-203580 did not inhibit IL-6 expression but exerted a stronger inhibitory effect on IL-8 expression. SB 203580 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 19074641-9 2009 Together, these data demonstrate that 1) acid is a potent inducer of IL-6 and IL-8 production in HET-1A cells; 2) MAPK and PKC signaling play a key regulatory role in acid-mediated IL-6 and IL-8 expression via NF-kappaB activation; and 3) the anti-inflammatory plant compound curcumin inhibits esophageal activation in response to acid. Curcumin 276-284 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 19221248-1 2009 OBJECTIVES: To evaluate the effect of curcumin on production of interleukin 6 (IL-6) and 8 (IL-8) in head and neck squamous cell carcinoma (HNSCC) cell lines and to determine the mechanism by which these effects are modulated. Curcumin 38-46 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 19221248-7 2009 MAIN OUTCOME MEASURES: Reverse transcription-polymerase chain reaction was performed to determine the effect of curcumin on the expression of IL-6 and IL-8. Curcumin 112-120 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 19221248-10 2009 Curcumin treatment resulted in inhibition of IKK activity and inhibition of IL-6 and IL-8 expression. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 18599066-3 2009 Palmitate induced secretion and mRNA expression of TNF-alpha, IL-8 and IL-1 beta, and enhanced lipopolysaccharide (LPS)-induced IL-1 beta secretion. Palmitates 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 19221248-11 2009 CONCLUSIONS: Curcumin significantly reduces IL-6 and IL-8 levels in HNSCC cell lines. Curcumin 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 18599066-9 2009 Knockdown of MyD88 reduced the palmitate-induced IL-8, but not TNF-alpha or IL-1 beta secretion. Palmitates 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 18977028-7 2009 Moreover, HL60-PMN cells secreted the potent neutrophil chemokine IL-8, also known as CXCL8, when exposed to chitosan and IL-8 levels increased with N-acetylation, and migration was inhibited by anti-IL-8 antibodies. Chitosan 109-117 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 18977028-7 2009 Moreover, HL60-PMN cells secreted the potent neutrophil chemokine IL-8, also known as CXCL8, when exposed to chitosan and IL-8 levels increased with N-acetylation, and migration was inhibited by anti-IL-8 antibodies. Chitosan 109-117 C-X-C motif chemokine ligand 8 Homo sapiens 86-91 19208784-6 2009 Thrombin, vascular endothelial growth factor and interleukin-8 synergistically augment angiogenesis in a milieu of reactive oxygen species-induced endothelial cell activation. Reactive Oxygen Species 115-138 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 19175605-0 2009 Prostaglandin E(2) couples through EP(4) prostanoid receptors to induce IL-8 production in human colonic epithelial cell lines. Prostaglandins E 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 19175605-4 2009 The aim of this study was to identify the role of the EP(2) and EP(4) receptor subtype(s) on two human colonic epithelial cell lines (Caco-2 and T84), in regulating PGE(2)-induced IL-8 production. Dinoprostone 165-171 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 19175605-8 2009 KEY RESULTS: PGE(2) had the highest affinity for the EP(4) receptor subtype and promoted a robust stimulation of cAMP-dependent IL-8 synthesis. Prostaglandins E 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 19175605-8 2009 KEY RESULTS: PGE(2) had the highest affinity for the EP(4) receptor subtype and promoted a robust stimulation of cAMP-dependent IL-8 synthesis. Cyclic AMP 113-117 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 19175605-10 2009 CONCLUSIONS AND IMPLICATIONS: These findings suggest that initiation and progression of colonic inflammation induced by IL-8 could be mediated, at least in part, by PGE(2) acting via the EP(4) receptor subtype. Prostaglandins E 165-168 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 19158563-8 2009 Tear IL-6 and IL-8 levels were significantly higher in patients with CCh than in controls (P <or= 0.001). 1-acetyl-2-(coumariniminecarboxamide-3-yl)hydrazine 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 18936140-14 2009 Inhibition of NF-kappaB with BAY 11-7082 reduced IL-8 but not VEGF induction. 3-(4-methylphenylsulfonyl)-2-propenenitrile 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 19015376-5 2009 The rapid and strong release of reactive oxygen species and preformed intragranular mediators (myeloperoxidase and IL-8) is followed by a later TNF-alpha, IL-1beta, and IL-8 synthesis. Reactive Oxygen Species 32-55 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19015376-5 2009 The rapid and strong release of reactive oxygen species and preformed intragranular mediators (myeloperoxidase and IL-8) is followed by a later TNF-alpha, IL-1beta, and IL-8 synthesis. Reactive Oxygen Species 32-55 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 19449765-16 2009 In addition, NO2 had a significant effect on bronchial reactivity and on the amount of interleukin-8 (IL-8) in induced sputum; it also modified the UFP effect on EBC pH and the EC effect on exhaled nitric oxide (eNO). Nitrogen Dioxide 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 87-100 19449765-16 2009 In addition, NO2 had a significant effect on bronchial reactivity and on the amount of interleukin-8 (IL-8) in induced sputum; it also modified the UFP effect on EBC pH and the EC effect on exhaled nitric oxide (eNO). Nitrogen Dioxide 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 18996182-0 2009 Norepinephrine upregulates VEGF, IL-8, and IL-6 expression in human melanoma tumor cell lines: implications for stress-related enhancement of tumor progression. Norepinephrine 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 19138532-3 2009 The results revealed that DEX nonspecifically and dose-dependently inhibited the production of 12 cytokines (IL-2, IFN-gamma, TNF-alpha, IL-8, IL-1beta, IL-17, IL-4, IL-5, IL-6, IL-10, IL-13, and G-CSF). Dexamethasone 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 18776171-3 2009 RSV blocked 10,12 CLA induction of the inflammatory response by preventing activation of extracellular signal-related kinase and induction of inflammatory gene expression (i.e., IL-6, IL-8, IL-1beta) within 12 h. Similarly, RSV suppressed 10,12 CLA-mediated activation of the inflammatory prostaglandin pathway involving phospholipase A(2), cyclooxygenase-2, and PGF(2alpha). Resveratrol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 19262007-5 2009 Our results demonstrate that a combination of insulin and glutamine are significantly more effective in reducing the expression of IL-8, TNF-alpha and HO-1 than insulin or glutamine alone. Glutamine 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 19262007-5 2009 Our results demonstrate that a combination of insulin and glutamine are significantly more effective in reducing the expression of IL-8, TNF-alpha and HO-1 than insulin or glutamine alone. Glutamine 172-181 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 19229322-5 2009 Our present findings demonstrate a rapid and HMB-PP-dependent crosstalk between Vgamma9/Vdelta2 T cells and autologous monocytes that results in the immediate production of inflammatory mediators including the cytokines interleukin (IL)-6, interferon (IFN)-gamma, tumor necrosis factor (TNF)-alpha, and oncostatin M (OSM); the chemokines CCL2, CXCL8, and CXCL10; and TNF-related apoptosis-inducing ligand (TRAIL). 4-hydroxy-3-methylbut-2-enyl pyrophosphate 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 344-349 19657754-9 2009 Secretion of IL-8 from cultured cervical fibroblasts was significantly increased after treatment with low molecular weight heparin. Heparin 123-130 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 19028451-5 2009 IL-8 up-regulation in response to HSP90 was also attenuated by IkappaB, rasveratrol, curcumin, diphenyleneiodium, N-acetylcystein, U0126, and SB202190. rasveratrol 72-83 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19028451-5 2009 IL-8 up-regulation in response to HSP90 was also attenuated by IkappaB, rasveratrol, curcumin, diphenyleneiodium, N-acetylcystein, U0126, and SB202190. Curcumin 85-93 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19028451-5 2009 IL-8 up-regulation in response to HSP90 was also attenuated by IkappaB, rasveratrol, curcumin, diphenyleneiodium, N-acetylcystein, U0126, and SB202190. diphenyleneiodium 95-112 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19028451-5 2009 IL-8 up-regulation in response to HSP90 was also attenuated by IkappaB, rasveratrol, curcumin, diphenyleneiodium, N-acetylcystein, U0126, and SB202190. N-Acetyl-L-cysteine 114-129 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19028451-5 2009 IL-8 up-regulation in response to HSP90 was also attenuated by IkappaB, rasveratrol, curcumin, diphenyleneiodium, N-acetylcystein, U0126, and SB202190. U 0126 131-136 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19028451-5 2009 IL-8 up-regulation in response to HSP90 was also attenuated by IkappaB, rasveratrol, curcumin, diphenyleneiodium, N-acetylcystein, U0126, and SB202190. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 142-150 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19034732-12 2009 The levels of IL-8 were higher following treatment with misoprostol compared to IMN and controls. Misoprostol 56-67 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 19239157-6 2009 Taurine also inhibited the TNF-alpha-induced secretion of IL-8 (a human homologue of MIP-2) from human intestinal epithelial Caco-2 cells. Taurine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 19567187-0 2009 [Effects of erythromycin on the synthesis of interleukin-8 and gamma-glutamylcysteine synthetase induced by 4-hydroxynonenal in the bronchial epithelial cells]. Erythromycin 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 19567187-0 2009 [Effects of erythromycin on the synthesis of interleukin-8 and gamma-glutamylcysteine synthetase induced by 4-hydroxynonenal in the bronchial epithelial cells]. 4-hydroxy-2-nonenal 108-124 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 19567187-1 2009 OBJECTIVE: This study was to explore the role of erythromycin on the synthesis of interleukin-8 (IL-8) and gamma-GCS treated by 4-hydroxynonenal (4-HNE) in bronchial epithelial cells (16-HBE). Erythromycin 49-61 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 19567187-1 2009 OBJECTIVE: This study was to explore the role of erythromycin on the synthesis of interleukin-8 (IL-8) and gamma-GCS treated by 4-hydroxynonenal (4-HNE) in bronchial epithelial cells (16-HBE). Erythromycin 49-61 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 19567187-1 2009 OBJECTIVE: This study was to explore the role of erythromycin on the synthesis of interleukin-8 (IL-8) and gamma-GCS treated by 4-hydroxynonenal (4-HNE) in bronchial epithelial cells (16-HBE). 4-hydroxy-2-nonenal 128-144 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 19567187-5 2009 (3) The effects of PD98059 and erythromycin on the expression of gamma-GCS, gamma-GCS mRNA, IL-8 and erythromycin on AP-1 combining activity by the 4-HNE were all detected. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 19567187-5 2009 (3) The effects of PD98059 and erythromycin on the expression of gamma-GCS, gamma-GCS mRNA, IL-8 and erythromycin on AP-1 combining activity by the 4-HNE were all detected. Erythromycin 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 19567187-13 2009 Erythromycin could inhibit the synthesis of IL-8 by blocking AP-1 pathway. Erythromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 19098936-7 2009 Additionally, 15d-PGJ2 at 2.5 and 5 micromol/L and TGL at 2.5 micromol/L inhibited TGF-beta1-induced expression of IL-8. 15-deoxyprostaglandin J2 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19098936-7 2009 Additionally, 15d-PGJ2 at 2.5 and 5 micromol/L and TGL at 2.5 micromol/L inhibited TGF-beta1-induced expression of IL-8. Troglitazone 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 19657754-11 2009 CONCLUSIONS: A possible underlying mechanism for the shortened labor time after low molecular weight heparin treatment is enhanced myometrial contractility and an increased IL-8 secretion in cervical fibroblast, mimicking the final cervical ripening in vivo. Heparin 101-108 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 19938227-7 2009 Furthermore, resveratrol inhibited extracellular signal-regulated kinase (ERK) and p38 MAPK phosphorylation, IkappaBalpha degradation, NF-kappaB activation and cyclooxygenase (COX)-2 expression, which suggest that resveratrol inhibits IL-8 secretion by blocking MAPK phosphorylation and NF-kappaB activation. Resveratrol 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 19938227-0 2009 Anti-inflammatory effect of resveratrol by inhibition of IL-8 production in LPS-induced THP-1 cells. Resveratrol 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 19938227-3 2009 To gain insight into the biological effects of resveratrol, we examined its influence on LPS-induced IL-8 production in the human monocytic cell line, THP-1. Resveratrol 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 19204390-0 2009 Fluoride retention in proximal plaque and saliva using two NaF dentifrices containing 5,000 and 1,450 ppm F with and without water rinsing. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 19938227-6 2009 Resveratrol inhibited LPS-induced IL-8 production in a dose-dependent manner. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 18635816-10 2009 The reducing agent N-acetyl-cysteine decreases IL8 message and promoter H4 acetylation to non-CF levels, suggesting that oxidative stress contributes to IL8 expression in these models. Acetylcysteine 19-36 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 18635816-10 2009 The reducing agent N-acetyl-cysteine decreases IL8 message and promoter H4 acetylation to non-CF levels, suggesting that oxidative stress contributes to IL8 expression in these models. Acetylcysteine 19-36 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 19526316-7 2009 HGF-induced up-regulations of Egr-1, VEGF, and IL-8 were inhibited by the pretreatment with an MEK inhibitor, PD098059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 110-118 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 19158539-8 2009 In addition, in patients with FM, IL-8 serum level correlated with nicotine consumption (r=0.471, P=0.042). Nicotine 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 18996370-4 2009 Microarray analysis using a tetracycline-inducible LMX1B expression system in HeLa cells revealed that a subset of NF-kappaB target genes, including IL-6 and IL-8, are upregulated in LMX1B-expressing cells. Tetracycline 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 18663553-6 2009 In the case of IL-8, its serum levels significantly diminished after 6 months of therapy with leflunomide (p < 0.01) and remained stable to the end of the study. Leflunomide 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 20003352-12 2009 A significant inverse association was found between IL-6, IL-8 and PaO2 in critical patients. pao2 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 19439970-5 2009 RESULTS: A significant correlation between norepinephrine support and IL-6 plasma concentrations was shown at the separation from CPB (k = 0.742) and 12 h after it (k = 0.801) as well as between norepinephrine support and IL-8 concentrations 12 h after the separation from CPB. Norepinephrine 43-57 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 19246914-4 2009 Additionally, in light of the stimulatory effect of homocysteine on the production of IL-8, we also sought to determine whether the methylenetetrahydrofolate reductase (MTHFR) gene 677 C/T variant, a genetic modifier of the serum homocysteine level, may interact with the IL-8 -251 polymorphism in determining the AD risk. Homocysteine 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 19551959-4 2009 The treatment with biltricid allow to decrease the TNF alpha, IL-1beta, IL-8 levels and to increase IL-4 level, especially in patients with combination of chronic opisthorhosis and Helicobacter pylori associated gastritis. biltricid 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 19053024-0 2009 Selective association of plasma non-esterified fatty acid species with circulating interleukin-8 concentrations in humans. Fatty Acids 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 19053024-7 2009 The correlations of myristate, oleate, and the sum of all omega3-polyunsaturated NEFA with interleukin-8 were independent of plasma tumour necrosis factor-alpha and overall adiposity. Myristic Acid 20-29 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 19053024-8 2009 Our data demonstrate close and selective associations of oleate, myristate, and omega3-polyunsaturated NEFA with plasma concentrations of the pro-inflammatory chemokine interleukin-8. omega3-polyunsaturated nefa 80-107 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 19439980-9 2009 RESULTS: Budesonide inhibited the release of TNF-alpha, IL-6 and IL-8 from sPLA(2)-stimulated macrophages in a concentration-dependent manner. Budesonide 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 19053024-7 2009 The correlations of myristate, oleate, and the sum of all omega3-polyunsaturated NEFA with interleukin-8 were independent of plasma tumour necrosis factor-alpha and overall adiposity. polyunsaturated nefa 65-85 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 19053024-8 2009 Our data demonstrate close and selective associations of oleate, myristate, and omega3-polyunsaturated NEFA with plasma concentrations of the pro-inflammatory chemokine interleukin-8. Oleic Acid 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 19053024-8 2009 Our data demonstrate close and selective associations of oleate, myristate, and omega3-polyunsaturated NEFA with plasma concentrations of the pro-inflammatory chemokine interleukin-8. Myristic Acid 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 19027816-6 2009 Resveratrol treatment effectively prevented increased production of intracellular reactive oxygen species (iROS) and inflammatory markers (IL1alpha, IL6, IL8, and ELAM-1), and reduced expression of the senescence markers sa-beta-gal, lipofuscin, and accumulation of carbonylated proteins. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 154-157 19038366-0 2009 Ghrelin inhibits interleukin-8 production induced by hydrogen peroxide in A549 cells via NF-kappaB pathway. Ghrelin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 17-30 19038366-0 2009 Ghrelin inhibits interleukin-8 production induced by hydrogen peroxide in A549 cells via NF-kappaB pathway. Hydrogen Peroxide 53-70 C-X-C motif chemokine ligand 8 Homo sapiens 17-30 19038366-3 2009 We examined whether ghrelin inhibits the proinflammatory cytokine interleukin-8 production induced by hydrogen peroxide (H2O2) in human lung epithelia cell line A549 and which mechanism is related with this effect of ghrelin. Ghrelin 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 19038366-3 2009 We examined whether ghrelin inhibits the proinflammatory cytokine interleukin-8 production induced by hydrogen peroxide (H2O2) in human lung epithelia cell line A549 and which mechanism is related with this effect of ghrelin. Hydrogen Peroxide 102-119 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 19038366-3 2009 We examined whether ghrelin inhibits the proinflammatory cytokine interleukin-8 production induced by hydrogen peroxide (H2O2) in human lung epithelia cell line A549 and which mechanism is related with this effect of ghrelin. Hydrogen Peroxide 121-125 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 19038366-7 2009 Cells treated with H2O2 (50 microM) exhibited significantly higher interleukin-8 production and ghrelin receptor mRNA expression compared with cells treated with vehicle alone (P < 0.05). Hydrogen Peroxide 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 19038366-8 2009 Ghrelin inhibited H2O2-induced interleukin-8 production by A549 at both mRNA and protein levels in a concentration-dependent manner (P < 0.05). Ghrelin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 19038366-8 2009 Ghrelin inhibited H2O2-induced interleukin-8 production by A549 at both mRNA and protein levels in a concentration-dependent manner (P < 0.05). Hydrogen Peroxide 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 19038366-10 2009 Together, these results suggest that ghrelin inhibits H2O2-induced interleukin-8 production in A549 cells by targeting on NF-kappaB pathway, but not by directly scavenging intracellular ROS. Ghrelin 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 19038366-10 2009 Together, these results suggest that ghrelin inhibits H2O2-induced interleukin-8 production in A549 cells by targeting on NF-kappaB pathway, but not by directly scavenging intracellular ROS. Hydrogen Peroxide 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 19494510-12 2009 CONCLUSION: These data showed that 15d-PGJ2 is a potent inducer of IL-8 and GM-CSF production through ERK1/2 kinase activation, but this is independent of CRTH2 or PPARgamma activation. 15-deoxy-delta(12,14)-prostaglandin J2 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 19494510-0 2009 15-Deoxy-Delta(12,14)-prostaglandin J2 induces IL-8 and GM-CSF in a human airway epithelial cell line (NCI-H292). 15-deoxy-delta(12,14)-prostaglandin J2 0-38 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 19494510-4 2009 Although our studies have shown that PGD2 (metabolic precursor of 15d-PGJ2) induces IL-8 and GM-CSF production, the role of 15d-PGJ2 (metabolite of PGD2) is unknown in human bronchial epithelial cells. Prostaglandin D2 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 19494510-4 2009 Although our studies have shown that PGD2 (metabolic precursor of 15d-PGJ2) induces IL-8 and GM-CSF production, the role of 15d-PGJ2 (metabolite of PGD2) is unknown in human bronchial epithelial cells. 15-deoxy-delta(12,14)-prostaglandin J2 66-74 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 19494510-8 2009 RESULTS: We demonstrated that 15d-PGJ2 induced production of IL-8 and GM-CSF from NCI-H292. 15-deoxy-delta(12,14)-prostaglandin J2 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 20131677-8 2009 The increase in Sa and bulk tissue loss caused by an erosive challenge followed by brushing was markedly reduced by pre-treatment with sodium fluoride (NaF) in a concentration-dependent manner. sa 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 20069129-0 2009 Reduction of monocyte chemoattractant protein-1 and interleukin-8 levels by ticlopidine in TNF-alpha stimulated human umbilical vein endothelial cells. Ticlopidine 76-87 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 19489187-5 2009 The study also showed that this new arginine toothpaste provided significantly greater reductions (p < 0.05) in dentin hypersensitivity in response to tactile (16.2%, 22.4%, and 21.4%) and air blast (16.2%, 29.2%, and 63.4%) stimuli than the benchmark commercial toothpaste containing 2% potassium ion and 1450 ppm NaF in a silica base, after two, four, and eight weeks of product use, respectively. Arginine 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 318-321 19489188-5 2009 The study also showed that this new arginine toothpaste provided significantly greater reductions (p < 0.05) in dentin hypersensitivity in response to tactile (37.0%, 30.0%, and 12.2%) and air blast (23.9%, 32.0%, and 29.3%) stimuli than the commercial sensitive toothpaste containing 2% potassium ion and 1450 ppm fluoride as NaF in a silica base, after two weeks, four weeks, and eight weeks of product use, respectively. Arginine 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 330-333 20069129-8 2009 These results suggest that ticlopidine decreased TNF-alpha induced MCP-1, IL-8, and VCAM-1 levels in HUVECs, and monocyte adhesion. Ticlopidine 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 19591336-7 2009 RESULTS: A good fluoride dose-response was established for EFU and REM, with NaF delivering greater EFU and REM than NaF-675, which was superior to NaF-0 (p < 0.05). Fluorides 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 19591336-12 2009 The new dentifrice NaF showed superior predicted anticaries potential compared to the two commercial dentifrices AmF and SnNaF in this model, which demonstrates the importance of fluoride compound and formulation excipients on driving anticaries potential in vitro. Fluorides 179-187 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 20131677-8 2009 The increase in Sa and bulk tissue loss caused by an erosive challenge followed by brushing was markedly reduced by pre-treatment with sodium fluoride (NaF) in a concentration-dependent manner. Sodium Fluoride 135-150 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 20131677-12 2009 CONCLUSION: The utility of NaF, whether delivered from simple solution or toothpaste, to reduce citric acid-mediated surface roughening and bulk tissue loss has been clearly demonstrated. Citric Acid 96-107 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 18690522-0 2009 Roles of reactive oxygen species in CXCL8 and CCL2 expression in response to the 30-kDa antigen of Mycobacterium tuberculosis. Reactive Oxygen Species 9-32 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 20131678-6 2009 RESULTS: Fluoride uptake by incipient erosive lesions treated with toothpastes containing NaF was quantitatively compared by DSIMS and found to be directly proportional to the fluoride concentration over the studied range (0-1400 ppm). Fluorides 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 18690522-3 2009 MATERIALS AND METHODS: In this study, we investigated the role of ROS in the activation of mitogen-activated protein kinases (MAPKs) and secretion of the CXC chemokine ligand 8 (CXCL8) and CC chemokine ligand 2 (CCL2) by human monocytes stimulated with the 30-kDa Ag of M. tuberculosis H37Rv. Reactive Oxygen Species 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 154-176 20131678-6 2009 RESULTS: Fluoride uptake by incipient erosive lesions treated with toothpastes containing NaF was quantitatively compared by DSIMS and found to be directly proportional to the fluoride concentration over the studied range (0-1400 ppm). Fluorides 176-184 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 18690522-3 2009 MATERIALS AND METHODS: In this study, we investigated the role of ROS in the activation of mitogen-activated protein kinases (MAPKs) and secretion of the CXC chemokine ligand 8 (CXCL8) and CC chemokine ligand 2 (CCL2) by human monocytes stimulated with the 30-kDa Ag of M. tuberculosis H37Rv. Reactive Oxygen Species 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 178-183 19503841-0 2009 Persistently elevated level of IL-8 in Chlamydia trachomatis infected HeLa 229 cells is dependent on intracellular available iron. Iron 125-129 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 18690522-5 2009 In addition, the 30-kDa Ag activated mRNA and protein expression of CXCL8 and CCL2 in human primary monocytes through nicotinamide adenine dinucleotide phosphate (NADPH) oxidase-dependent ROS generation. NADP 118-161 C-X-C motif chemokine ligand 8 Homo sapiens 68-73 18690522-5 2009 In addition, the 30-kDa Ag activated mRNA and protein expression of CXCL8 and CCL2 in human primary monocytes through nicotinamide adenine dinucleotide phosphate (NADPH) oxidase-dependent ROS generation. Reactive Oxygen Species 188-191 C-X-C motif chemokine ligand 8 Homo sapiens 68-73 18690522-10 2009 CONCLUSION: These results indicate that TLR2-ROS signaling plays a crucial role in the 30-kDa Ag-mediated expression of CXCL8 and CCL2 in human monocytes. Reactive Oxygen Species 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 120-125 19109168-3 2009 Whether sex steroids affect IL-8 secretion of normal breast tissue or breast cancer is not known. Steroids 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 19109168-9 2009 In experimental breast cancer, estradiol increased IL-8 whereas the anti-estrogen tamoxifen inhibited the secretion of IL-8 both in vitro and extracellularly in vivo in tumors of nude mice. Estradiol 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 19109168-9 2009 In experimental breast cancer, estradiol increased IL-8 whereas the anti-estrogen tamoxifen inhibited the secretion of IL-8 both in vitro and extracellularly in vivo in tumors of nude mice. Tamoxifen 82-91 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 19926933-0 2009 Suppressive effect of an isoflavone fraction on tumor necrosis factor-alpha-induced interleukin-8 production in human intestinal epithelial Caco-2 cells. Isoflavones 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 19926933-2 2009 Among the soybean components, an isoflavone fraction (IFF) suppressed the TNF-alpha-induced IL-8 secretion by Caco-2 cells in a dose-dependent manner, whereas a soyasaponin fraction and soypeptide fraction had no significant effect on TNF-alpha-induced IL-8 secretion. Isoflavones 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 19926933-3 2009 The IL-8 secretion induced by hydrogen peroxide and by IL-1beta was not suppressed by IFF, suggesting that the inhibitory effect of isoflavone was specific for the TNF-alpha-induced regulation of IL-8. Hydrogen Peroxide 30-47 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 19926933-3 2009 The IL-8 secretion induced by hydrogen peroxide and by IL-1beta was not suppressed by IFF, suggesting that the inhibitory effect of isoflavone was specific for the TNF-alpha-induced regulation of IL-8. Isoflavones 132-142 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 20150959-4 2009 In the present study, the concentrations of IL-8 in culture supernatants of HeLa cells treated with ROS were determined by enzyme-linked immunosorbent assay. ros 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 20150959-7 2009 Enzyme-linked immunosorbent assays showed that IL-8 protein secretion was elevated in ROS-treated HeLa cells. ros 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 20150959-8 2009 When Fe(2+) was removed from these cells, IL-8 secretion was inhibited. ammonium ferrous sulfate 5-11 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 23230472-3 2009 The aim of this investigation was to evaluate fluoride uptake level of a locally prepared NaF rinse used in Iran"s school program during 2005. Fluorides 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 19503841-3 2009 We examined the effect of iron chelators on IL-8 production in HeLa 229 (cervix epitheloid cell, CCL2) cells infected with C. trachomatis. Iron 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 20150959-9 2009 Collectively, these results indicate that Fe(2+)-mediated Erk pathway activation is an important signal transduction pathway in ROS-induced IL-8 secretion in epithelial cells. ammonium ferrous sulfate 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 20150959-9 2009 Collectively, these results indicate that Fe(2+)-mediated Erk pathway activation is an important signal transduction pathway in ROS-induced IL-8 secretion in epithelial cells. ros 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 19503841-4 2009 IL-8 production was induced by Iron chelator DFO and Mimosine, however, synergy with chlamydial infection was obtained with DFO only. Iron 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19503841-4 2009 IL-8 production was induced by Iron chelator DFO and Mimosine, however, synergy with chlamydial infection was obtained with DFO only. Deferoxamine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19503841-4 2009 IL-8 production was induced by Iron chelator DFO and Mimosine, however, synergy with chlamydial infection was obtained with DFO only. Mimosine 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19503841-4 2009 IL-8 production was induced by Iron chelator DFO and Mimosine, however, synergy with chlamydial infection was obtained with DFO only. Deferoxamine 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 19503841-7 2009 These results indicate towards involvement of iron in chlamydia induced IL-8 production. Iron 46-50 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 19247502-8 2009 At baseline, CD significantly (p<0.05) induced IL-8 and NFkappaB reporter activities as compared to control cells suggesting a negative regulation of NFkappaB mediated IL-8 signaling by CFTR in cholesterol-rich lipid rafts. methyl-beta-cyclodextrin 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 18830568-4 2009 We first observed that the spontaneous release of suPAR by resting neutrophils was strongly and rapidly (within minutes) enhanced by calcium ionophore ionomycin and to a lesser extent when cells were primed with TNF-alpha and then stimulated with fMLP or IL-8. supar 50-55 C-X-C motif chemokine ligand 8 Homo sapiens 255-259 19246943-2 2009 In this study, we examined the effect of N-methyl-D-aspartate (NMDA) and sigma1-receptor ligands on the secretion of the proinflammatory chemokine interleukin 8 (IL-8) and the anti-inflammatory cytokine interleukin 10 (IL-10) in human leukemia Jurkat cells and peripheral blood lymphocytes (PBLs). N-Methylaspartate 41-61 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 19246943-2 2009 In this study, we examined the effect of N-methyl-D-aspartate (NMDA) and sigma1-receptor ligands on the secretion of the proinflammatory chemokine interleukin 8 (IL-8) and the anti-inflammatory cytokine interleukin 10 (IL-10) in human leukemia Jurkat cells and peripheral blood lymphocytes (PBLs). N-Methylaspartate 41-61 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 19246943-2 2009 In this study, we examined the effect of N-methyl-D-aspartate (NMDA) and sigma1-receptor ligands on the secretion of the proinflammatory chemokine interleukin 8 (IL-8) and the anti-inflammatory cytokine interleukin 10 (IL-10) in human leukemia Jurkat cells and peripheral blood lymphocytes (PBLs). N-Methylaspartate 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 19246943-2 2009 In this study, we examined the effect of N-methyl-D-aspartate (NMDA) and sigma1-receptor ligands on the secretion of the proinflammatory chemokine interleukin 8 (IL-8) and the anti-inflammatory cytokine interleukin 10 (IL-10) in human leukemia Jurkat cells and peripheral blood lymphocytes (PBLs). N-Methylaspartate 63-67 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 19246943-3 2009 We have shown that NMDA increased IL-8 and decreased IL-10 secretion and that sigma-ligands modulated the action of NMDA. N-Methylaspartate 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 19247502-8 2009 At baseline, CD significantly (p<0.05) induced IL-8 and NFkappaB reporter activities as compared to control cells suggesting a negative regulation of NFkappaB mediated IL-8 signaling by CFTR in cholesterol-rich lipid rafts. methyl-beta-cyclodextrin 13-15 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 19247502-8 2009 At baseline, CD significantly (p<0.05) induced IL-8 and NFkappaB reporter activities as compared to control cells suggesting a negative regulation of NFkappaB mediated IL-8 signaling by CFTR in cholesterol-rich lipid rafts. Cholesterol 197-208 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 19365107-10 2009 Upon tumor necrosis factor-alpha stimulation, IL-6 and IL-8 mRNA and protein levels in A549-PLA2G2D-Ser cells were elevated compared with those of A549-PLA2G2D-Gly cells. Serine 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 19365107-9 2009 A549-PLA2G2D-Ser cells spontaneously produced higher levels of interleukin (IL)-6 and IL-8 than A549-PLA2G2D-Gly cells. Serine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 19365107-11 2009 Upon hydrogen peroxide stimulation, IL-8 mRNA and protein levels in A549-PLA2G2D-Ser cells were higher than those of A549-PLA2G2D-Gly cells. Hydrogen Peroxide 5-22 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 19365107-11 2009 Upon hydrogen peroxide stimulation, IL-8 mRNA and protein levels in A549-PLA2G2D-Ser cells were higher than those of A549-PLA2G2D-Gly cells. Serine 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 19365107-12 2009 CONCLUSIONS: PLA2G2D-Ser enhances the expression of IL-6 and IL-8 compared with PLA2G2D-Gly. Serine 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 18951912-10 2009 Acrolein treatment led to activation and nuclear translocation of the transcription factor NF-kappaB and an increase in TNF-alpha, IL-6 and IL-8, but not MCP-1, mRNA. Acrolein 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 19139781-5 2009 RESULTS: Silymarin reduces significantly serum levels of IL-1 alpha and IL-8, C3 and C4 after 8 weeks compared to the pre-treatment levels. Silymarin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 19139781-9 2009 Adjunct use of silymarin with piroxicam results in significant reduction in both cytokines (IL-1 alpha and IL-8), and serum levels of C3 and C4. Silymarin 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 19139781-9 2009 Adjunct use of silymarin with piroxicam results in significant reduction in both cytokines (IL-1 alpha and IL-8), and serum levels of C3 and C4. Piroxicam 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 19247848-7 2009 In ATV-stimulated FLS a significant downregulation of proinflammatory cytokine (IL-6) and chemokine (IL-8) expression was detected (p<0.001). Atorvastatin 3-6 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 19050703-2 2008 In vitro experiments conducted on PC3 and human bone marrow endothelial cells (hBMECs) determined that administration of DEX (10 nM) reduced constitutive nuclear factor-kappaB (NF-kappaB) activity, decreasing interleukin (IL)-8, CXCL1 and VEGF gene expression in PC3 cells. Dexamethasone 121-124 C-X-C motif chemokine ligand 8 Homo sapiens 209-227 18824136-7 2009 Moreover, both promoter activity and release of IL-8 were inhibited by U0126 and curcumin, but not by SB202190, epigallocatechin 3-gallate and resveratrol. U 0126 71-76 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 18824136-7 2009 Moreover, both promoter activity and release of IL-8 were inhibited by U0126 and curcumin, but not by SB202190, epigallocatechin 3-gallate and resveratrol. Curcumin 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 19050703-3 2008 Dexamethasone also attenuated docetaxel-induced NF-kappaB and activator protein-1 transcription and reduced docetaxel-promoted expression/secretion of IL-8 and CXCL1 in PC3 and hBMECs. Docetaxel 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 19542657-4 2009 The iron nanotubes were fabricated in 1 M Na(2)SO(4) + 0.5 wt% NaF electrolyte by supplying constant electric currents of 50 mV/s, and holding the potential at 20, 40 and 60 V for 20 min. Iron 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 18840498-6 2008 Ethanol decreased LPS-stimulated IL-6, IL-8, TNF-alpha, and MCP-1 dose-dependently (all p<0.01). Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 19050703-3 2008 Dexamethasone also attenuated docetaxel-induced NF-kappaB and activator protein-1 transcription and reduced docetaxel-promoted expression/secretion of IL-8 and CXCL1 in PC3 and hBMECs. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 19012411-11 2008 Toxic shock syndrome toxin-1 residue D130 may contribute to binding an epithelial receptor, which allows it to penetrate the vaginal mucosa, induce interleukin-8, and cause toxic shock syndrome. d130 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 18854173-4 2008 The PAR2-triggered IL-8 release was suppressed by inhibitors of MEK (U0126) or PI3-kinase (LY294002), and PAR2 stimulation indeed activated the downstream kinases, ERK and Akt. U 0126 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 18854173-4 2008 The PAR2-triggered IL-8 release was suppressed by inhibitors of MEK (U0126) or PI3-kinase (LY294002), and PAR2 stimulation indeed activated the downstream kinases, ERK and Akt. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 91-99 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 19074906-8 2008 Furthermore, rapamycin not only drastically inhibited CXCL16-induced PCa cell invasion and growth but reduced secretion of IL-8 or VEGF levels and inhibited expression of other CXCR6 targets including CD44 and matrix metalloproteinase 3 in PCa cells. Sirolimus 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 19367948-1 2008 A novel method has been developed to prepare vesicles from aqueous solutions of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymer, by adding anionic surfactant sodium dodecyl sulfate (SDS) and inorganic salt NaF. poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymer 80-162 C-X-C motif chemokine ligand 8 Homo sapiens 241-244 19032233-8 2008 TNF-alpha-induced GRO-alpha and IL-8 were slightly attenuated by DEX treatment (reaches to 89% and 79%, respectively), whereas expressions of IP-10, ICAM-1 and VCAM-1 were significantly enhanced by the same treatment (up to 172%, 152% and 139%, respectively). Dexamethasone 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 18838587-8 2008 Colposcopy and biopsy studies indicate that GML does not alter normal mucosal integrity and does not induce inflammation; instead, GML reduces epithelial cell production of interleukin 8. monolaurin 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 173-186 18665800-0 2008 15d-PGJ2 upregulates synthesis of IL-8 in endothelial cells through induction of oxidative stress. 15-deoxyprostaglandin J2 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 19064561-10 2008 Only IL4, IL6, and IL8 had statistically significant correlations (Spearman rho, 0.42-0.94) between serum and acid citrate dextrose or heparin plasma levels. acid citrate dextrose 110-131 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 18665800-2 2008 It has been demonstrated that 15d-PGJ(2) potently increases the generation of interleukin-8 (IL-8) in human microvascular endothelial cells (HMEC-1s); however, the mechanism of this induction is not known. 15d-pgj 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 18665800-2 2008 It has been demonstrated that 15d-PGJ(2) potently increases the generation of interleukin-8 (IL-8) in human microvascular endothelial cells (HMEC-1s); however, the mechanism of this induction is not known. 15d-pgj 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 18665800-3 2008 The aim of the study was to find the pathway involved in 15d-PGJ(2)-mediated IL-8 stimulation. 2-(ETHOXYMETHYL)-4-(4-FLUOROPHENYL)-3-[2-(2-HYDROXYPHENOXY)PYRIMIDIN-4-YL]ISOXAZOL-5(2H)-ONE 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 19064561-10 2008 Only IL4, IL6, and IL8 had statistically significant correlations (Spearman rho, 0.42-0.94) between serum and acid citrate dextrose or heparin plasma levels. Heparin 135-142 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 19036603-7 2008 The mean percentage of the inhibition of IL-6, CXCL8/IL-8, CCL3/MIP-1alpha by bestatin at a concentration of 50 microg/mL was 71.2%, 29.7% and 61.0%, respectively. ubenimex 78-86 C-X-C motif chemokine ligand 8 Homo sapiens 47-52 19033802-3 2008 For a comprehensive morphologic and scintigraphic evaluation, a whole-body F-18 sodium fluoride (NaF) PET-CT was acquired. Sodium Fluoride 80-95 C-X-C motif chemokine ligand 8 Homo sapiens 97-100 19036603-7 2008 The mean percentage of the inhibition of IL-6, CXCL8/IL-8, CCL3/MIP-1alpha by bestatin at a concentration of 50 microg/mL was 71.2%, 29.7% and 61.0%, respectively. ubenimex 78-86 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 19036603-9 2008 The treatment with bestatin significantly inhibited the production of IL-6 and CXCL8/IL-8 by AM from patients with sarcoidosis. ubenimex 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 19036603-9 2008 The treatment with bestatin significantly inhibited the production of IL-6 and CXCL8/IL-8 by AM from patients with sarcoidosis. ubenimex 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 19186852-11 2008 The change of Area, deltaF and lg deltaQ of the lesions in NaF group and MFP group exhibited significant decreases than that of no-fluoride dentifrice group (P<0.05). Fluorides 131-139 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 19103522-6 2008 From a mechanistic point of view, by blocking independently Galphai protein or intracellular calcium, monocytes lose the ability to secrete CXCL8 in response to PROK1. Calcium 93-100 C-X-C motif chemokine ligand 8 Homo sapiens 140-145 19103523-9 2008 After treatment with 10 microM of gossypol, there was a 1.5-fold decrease in angiogenin and IL-8 levels and a 1.7- and 1.8-fold decrease in ENA-78 and GRO-alpha levels respectively, in DU-145 cells. Gossypol 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 18809662-10 2008 FlaA-induced IL-8 production in T84 cells was inhibited by the p38 inhibitor in combination with either the JNK or ERK inhibitors. flaa 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 18780829-3 2008 This study sought to determine the significance of CXCL8 signaling in regulating the response of AIPC cells to oxaliplatin, a drug whose activity is reportedly sensitive to NF-kappaB activity. Oxaliplatin 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 51-56 19022976-7 2008 Arg(high)/Gln(high) decreased the production of TNFalpha, IL-1beta, IL-8, and IL-6 (each P < 0.01). Arginine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 19022976-7 2008 Arg(high)/Gln(high) decreased the production of TNFalpha, IL-1beta, IL-8, and IL-6 (each P < 0.01). Glutamine 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 19022976-8 2008 Arg(low)/Gln(high) decreased IL-6 and IL-8 production (both P < 0.01), whereas Arg(high)/Gln(low) did not affect cytokine and NO production. Arginine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 19022976-8 2008 Arg(low)/Gln(high) decreased IL-6 and IL-8 production (both P < 0.01), whereas Arg(high)/Gln(low) did not affect cytokine and NO production. Glutamine 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 18780829-5 2008 In addition, oxaliplatin increased the transcription and secretion of CXCL8 and the related CXC-chemokine CXCL1 and increased the transcription and expression of CXC-chemokine receptors, especially CXC-chemokine receptor (CXCR) 2, which transduces the biological effects of CXCL8 and CXCL1. Oxaliplatin 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 70-75 18780829-5 2008 In addition, oxaliplatin increased the transcription and secretion of CXCL8 and the related CXC-chemokine CXCL1 and increased the transcription and expression of CXC-chemokine receptors, especially CXC-chemokine receptor (CXCR) 2, which transduces the biological effects of CXCL8 and CXCL1. Oxaliplatin 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 274-279 19055699-7 2008 CBA confirmed upregulation of IL-8 and show upregulation of IL-1beta in the tumours (P < 0.05). cba 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 18688800-5 2008 High glucose-induced MCP-1 and IL-8 mRNA expression levels also decreased by ABO. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 19046427-7 2008 The cell response to IL-8 was determined by measuring intracellular calcium concentration ([Ca2+](i)), cell contraction, migration and proliferation. Calcium 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 18789311-2 2008 In the present study, we demonstrated that reorganization of actin cytoskeleton induced by Cytochalasin D (CytD), an actin-polymerization inhibitor, enhanced il-8 gene expression induced by TNFalpha and LPS in HL-60 monocyte-like cells. Cytochalasin D 91-105 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 19132242-2 2008 Since nuclear factor-kappaB (NF-kappaB) is a major regulator of IL-8 transcription, we studied its activation in endothelial cells treated with E-LDL. e-ldl 144-149 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 18535203-6 2008 PMN chemotactic responses to formylmethionyl-leucyl-phenylalanine (fMLP) and IL-8 were dose-dependently inhibited by treatment with the PPAR-gamma ligands troglitazone and 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)) and by transfection of PMN-like HL-60 cells with a constitutively active PPAR-gamma construct. Troglitazone 155-167 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 18535203-6 2008 PMN chemotactic responses to formylmethionyl-leucyl-phenylalanine (fMLP) and IL-8 were dose-dependently inhibited by treatment with the PPAR-gamma ligands troglitazone and 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)) and by transfection of PMN-like HL-60 cells with a constitutively active PPAR-gamma construct. 15-deoxy-delta 172-186 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 18535203-6 2008 PMN chemotactic responses to formylmethionyl-leucyl-phenylalanine (fMLP) and IL-8 were dose-dependently inhibited by treatment with the PPAR-gamma ligands troglitazone and 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)) and by transfection of PMN-like HL-60 cells with a constitutively active PPAR-gamma construct. prostaglandin j 194-209 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 18981129-9 2008 In contrast to induction of the antimicrobial peptide, vitamin D attenuates dsRNA-induced expression of the NF-kappaB-driven gene IL-8. Vitamin D 55-64 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 18535203-6 2008 PMN chemotactic responses to formylmethionyl-leucyl-phenylalanine (fMLP) and IL-8 were dose-dependently inhibited by treatment with the PPAR-gamma ligands troglitazone and 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)) and by transfection of PMN-like HL-60 cells with a constitutively active PPAR-gamma construct. 2-(ETHOXYMETHYL)-4-(4-FLUOROPHENYL)-3-[2-(2-HYDROXYPHENOXY)PYRIMIDIN-4-YL]ISOXAZOL-5(2H)-ONE 218-221 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 18698005-3 2008 In the presence of exogenous PGE(2), peripheral blood mononuclear cells produced higher interleukin-17 (IL-17), C-C chemokine ligand 20 (CCL20)/macrophage inflammatory protein 3alpha (MIP-3alpha), CXC chemokine ligand 8 (CXCL8)/IL-8, and lower interferon-gamma and IL-22 levels than in control cultures. Prostaglandins E 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 197-219 19014534-0 2008 IL-1beta differently involved in IL-8 and FGF-2 release in crystalline silica-treated lung cell co-cultures. Silicon Dioxide 71-77 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 19014534-2 2008 The aim of the present study was to investigate the effect of crystalline silica on the release of the fibrosis- and angiogenesis-related mediator FGF-2 and the pro-inflammatory mediator IL-8, and how IL-1beta and TNF-alpha were involved in this release from various mono- and co-cultures of monocytes, pneumocytes and endothelial cells. Silicon Dioxide 74-80 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 19014534-3 2008 RESULTS: Silica exposure induced an increase of IL-8 release from monocytes and from pneumocytes alone, and the FGF-2 level in the medium increased upon silica exposure of pneumocytes. Silicon Dioxide 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 19014534-10 2008 CONCLUSION: IL-1beta seems to be differently involved in the silica-induced release of IL-8 and FGF-2 in different lung cell cultures. Silicon Dioxide 61-67 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 19014534-11 2008 Whereas the silica-induced IL-8 release is regulated via an IL-1-receptor-mediated mechanism, IL-1beta is suggested only indirectly to affect the silica-induced FGF-2 release by counteracting pneumocyte loss. Silicon Dioxide 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 18976019-9 2008 Interleukin 6 concentrations were stable for 8 hours in all blood types, whereas interleukin 8 concentrations were stable only in EDTA plasma and were strongly increasing in heparin plasma and serum. Edetic Acid 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 18976019-9 2008 Interleukin 6 concentrations were stable for 8 hours in all blood types, whereas interleukin 8 concentrations were stable only in EDTA plasma and were strongly increasing in heparin plasma and serum. Heparin 174-181 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 18474668-7 2008 Exposure to gamma-iE-DAP at the apical surface of differentiated, polarized cultures resulted in activation of the innate immune response in an NOD1- and RIP2-dependent manner, resulting in release of IL-6 and IL-8. N(2)-(gamma-D-glutamyl)-meso-2,2'-diaminopimelic acid 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 18996285-7 2008 RESULTS: NF-kappaB p65 antisense oligonucleotides resulted in downregulation of NF-kappaB p65 expression, blocked the expression of IL-1beta mRNA and IL-8 mRNA, and strikingly reduced the production of IL-1beta and IL-8. Oligonucleotides 33-49 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 18996285-7 2008 RESULTS: NF-kappaB p65 antisense oligonucleotides resulted in downregulation of NF-kappaB p65 expression, blocked the expression of IL-1beta mRNA and IL-8 mRNA, and strikingly reduced the production of IL-1beta and IL-8. Oligonucleotides 33-49 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 18975306-10 2008 ACh significantly reduced the production of IL-6, CXCL8, CCL2, CCL3, CCL5, and granulocyte colony-stimulating factor by IL-1-stimulated FLS. Acetylcholine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 50-55 18698005-3 2008 In the presence of exogenous PGE(2), peripheral blood mononuclear cells produced higher interleukin-17 (IL-17), C-C chemokine ligand 20 (CCL20)/macrophage inflammatory protein 3alpha (MIP-3alpha), CXC chemokine ligand 8 (CXCL8)/IL-8, and lower interferon-gamma and IL-22 levels than in control cultures. Prostaglandins E 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 221-226 18698005-3 2008 In the presence of exogenous PGE(2), peripheral blood mononuclear cells produced higher interleukin-17 (IL-17), C-C chemokine ligand 20 (CCL20)/macrophage inflammatory protein 3alpha (MIP-3alpha), CXC chemokine ligand 8 (CXCL8)/IL-8, and lower interferon-gamma and IL-22 levels than in control cultures. Prostaglandins E 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 228-232 18617617-0 2008 Lysophosphatidic acid mediates interleukin-8 expression in human endometrial stromal cells through its receptor and nuclear factor-kappaB-dependent pathway: a possible role in angiogenesis of endometrium and placenta. lysophosphatidic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 19085374-7 2008 Besifloxacin significantly inhibited IL-1beta-induced cytokine release in a dose-dependent manner, with a comparable (IL-8) or better (G-CSF, GM-CSF, IL-6, MCP-1, MIP-1beta, TGF-alpha, and TNF-alpha) efficacy compared to moxifloxacin. besifloxacin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 18617617-11 2008 LPA enhanced IL-8 expression in a dose- and time-dependent manner, whereas vascular endothelial growth factor or IL-6 expression was not affected by LPA treatment. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 18617617-15 2008 Through the LPA1 receptor, LPA induces IL-8 expression via a nuclear factor-kappaB-dependent signal pathway. lysophosphatidic acid 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 18697197-4 2008 Treatment of tumor cells with doxorubicin and cisplatin resulted in a substantial increase in the production of IL-6, CXCL8, CCL2, CCL5, BFGF, G-CSF and VEGF. Doxorubicin 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 19075349-5 2008 We have found that in peripheral blood lymphocytes glutamate at the concentrations within normal plasma levels (1 x 10(-5) M), as well as at lower concentration (0.3 x 10(-6) M) changes the secretion of immunosuppressive cytokine IL-10, whereas synthesis of proinflammatory chemokine, IL-8 did not changed significantly. Glutamic Acid 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 285-289 18653652-7 2008 Tricultures with EAHY926 released more G-CSF, MIP-1alpha, IL-8 and MIP-1beta than the EAHY926 single culture. eahy926 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 19001436-7 2008 These results suggest that tanshinone I exhibits anticancer effects both in vitro and in vivo and that these effects are mediated at least partly through the interleukin-8, Ras-mitogen-activated protein kinase, and Rac1 signaling pathways. tanshinone 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 19109744-7 2008 Significant inhibition (P > 0.05) of TNF-alpha, IL-6 and IL-8 at non-toxic of digoxin concentration (< 100 nM) and DLIF (10 nM digoxin equivalent (de)) was observed whereas no such effect was seen for IL-10. Digoxin 81-88 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 19109744-7 2008 Significant inhibition (P > 0.05) of TNF-alpha, IL-6 and IL-8 at non-toxic of digoxin concentration (< 100 nM) and DLIF (10 nM digoxin equivalent (de)) was observed whereas no such effect was seen for IL-10. Digoxin 133-140 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 18971093-9 2008 Azithromycin caused a significant decrease in the LPS-stimulated IL-8 and GM-CSF release. Azithromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 18728240-0 2008 Clotrimazole ameliorates intestinal inflammation and abnormal angiogenesis by inhibiting interleukin-8 expression through a nuclear factor-kappaB-dependent manner. Clotrimazole 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 18728240-2 2008 In the present study, we investigated the fact that clotrimazole (CLT) inhibits intestinal inflammation, and the inhibitory action is mediated through suppression of IL-8 expression. Clotrimazole 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 18728240-2 2008 In the present study, we investigated the fact that clotrimazole (CLT) inhibits intestinal inflammation, and the inhibitory action is mediated through suppression of IL-8 expression. Clotrimazole 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 18728240-6 2008 Furthermore, cotreatment with CLT and pyrrolidine dithiocarbamate, a NF-kappaB inhibitor, synergistically reduced the NF-kappaB transcriptional activity as well as IL-8 expression. Clotrimazole 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 18728240-6 2008 Furthermore, cotreatment with CLT and pyrrolidine dithiocarbamate, a NF-kappaB inhibitor, synergistically reduced the NF-kappaB transcriptional activity as well as IL-8 expression. pyrrolidine dithiocarbamic acid 38-65 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 18779317-9 2008 Consequently, induction of interleukin-8 and beta interferon after poly(I-C) stimulation was impaired in HCT116 p53(-/-) cells. Poly I-C 67-76 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 18697197-4 2008 Treatment of tumor cells with doxorubicin and cisplatin resulted in a substantial increase in the production of IL-6, CXCL8, CCL2, CCL5, BFGF, G-CSF and VEGF. Cisplatin 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 18541460-9 2008 While neutrophil cell counts and IL-8 levels decreased, the LXA(4) levels significantly increased after antibiotics therapy and were inversely correlated with IL-8 levels. lxa( 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 18941244-8 2008 The p38 and ERK pathway inhibitors SB203580 and U0126 reversed the repressive effect of IL-17 on CXCL10 mRNA abundance and promoter activity and also reversed the inductive effect of IL-17 on CXCL8 mRNA, indicating that MAPK signaling mediates both the transcriptional repression of CXCL10 and the stabilization of CXCL8 mRNA by IL-17. SB 203580 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 192-197 18941244-8 2008 The p38 and ERK pathway inhibitors SB203580 and U0126 reversed the repressive effect of IL-17 on CXCL10 mRNA abundance and promoter activity and also reversed the inductive effect of IL-17 on CXCL8 mRNA, indicating that MAPK signaling mediates both the transcriptional repression of CXCL10 and the stabilization of CXCL8 mRNA by IL-17. SB 203580 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 315-320 18941244-8 2008 The p38 and ERK pathway inhibitors SB203580 and U0126 reversed the repressive effect of IL-17 on CXCL10 mRNA abundance and promoter activity and also reversed the inductive effect of IL-17 on CXCL8 mRNA, indicating that MAPK signaling mediates both the transcriptional repression of CXCL10 and the stabilization of CXCL8 mRNA by IL-17. U 0126 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 192-197 18941244-8 2008 The p38 and ERK pathway inhibitors SB203580 and U0126 reversed the repressive effect of IL-17 on CXCL10 mRNA abundance and promoter activity and also reversed the inductive effect of IL-17 on CXCL8 mRNA, indicating that MAPK signaling mediates both the transcriptional repression of CXCL10 and the stabilization of CXCL8 mRNA by IL-17. U 0126 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 315-320 18941244-9 2008 The EGFR kinase inhibitor AG1478 partially reversed the effects of IL-17 on CXCL8 and CXCL10 mRNA, demonstrating a role for EGFR in downstream IL-17 signaling. RTKI cpd 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 76-81 18587146-3 2008 Stepwise multiple regression analyses of factors including age, occupation, years of employment, alcohol drinking behaviour, physical activity, nutritional balance and cigarette smoking parameters showed that LECT was a positively significant predictor (Partial r = 0.0005, P < 0.05) of the comet tail moment. Alcohols 97-104 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 18587146-4 2008 In consideration of the high correlation between LECT and LECN (Y(tar) = 12.53 X(nicotine) -7.23, r = 0.995, P < 0.0001), these results suggest that levels of exposure to cigarette tar or nicotine (mg/day) would be a sensitive parameter in appreciation of genotoxicity of cigarette smoking in these male Japanese smokers. Nicotine 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 18764914-4 2008 RESULTS: All mediators were detectable in serum and all but IL-8 were detectable in EBC. NSC638702 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 18669446-3 2008 Treatment of MCF-7 cells with the HDAC inhibitor trichostatin A (TSA) led to a strong up-regulation of IL-8 protein and RNA levels in MCF-7 cells. trichostatin A 49-63 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 18669446-3 2008 Treatment of MCF-7 cells with the HDAC inhibitor trichostatin A (TSA) led to a strong up-regulation of IL-8 protein and RNA levels in MCF-7 cells. trichostatin A 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 18669446-9 2008 TSA increased binding of acetylated histone 3 to the IL-8 gene promoter. trichostatin A 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 18701168-4 2008 It also enhanced neutrophil IL-8 production induced by double-stranded bacterial DNA, methylated single-stranded DNA, plasmid DNA, and phosphorothioated-CpG and non-CpG-oligodeoxynucleotides. phosphorothioated-cpg 135-156 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 19084961-8 2008 Both Pg-LPS and E-LPS induced IL-8 secretion by THP-1 cells (P<0.01), but only Pg-LPS showed the similar effect on HGF-1 cells (P<0.01). pg-lps 5-11 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 18277946-4 2008 Both PAR2-AP and the endogenous PAR2 activator trypsin caused concentration- and time-dependent increase in endothelial IL-8 production, and this effect was concentration dependently and selectively attenuated by the p38 mitogen-activated protein kinase (MAPK) inhibitor SB203580. SB 203580 271-279 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 19010201-0 2008 Analysis of interleukin-6 and interleukin-8 in lung transplantation: correlation with nitric oxide administration. Nitric Oxide 86-98 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 19084961-8 2008 Both Pg-LPS and E-LPS induced IL-8 secretion by THP-1 cells (P<0.01), but only Pg-LPS showed the similar effect on HGF-1 cells (P<0.01). e-lps 16-21 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 18675368-9 2008 So echinomycin-induced apoptosis in HT-29 cells occurs via NF-kappaB activation independent of caspase-3 activation modulating the resultant-linked key chemokine IL-8 expression and echinomycin-induced apoptosis is NF-kappaB-dependant and directly related to NF-kappaB activation, consequently regulating IL-8 expression. Echinomycin 3-14 C-X-C motif chemokine ligand 8 Homo sapiens 305-309 18772138-0 2008 Regulation of interleukin-8 gene at a distinct site of its promoter by CCAAT enhancer-binding protein homologous protein in prostaglandin E2-treated human T cells. Dinoprostone 124-140 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 18772138-2 2008 We have previously shown that in human T lymphocytes the CHOP phosphorylation induced by prostaglandin E(2) (PGE(2))-increased interleukin-8 (IL-8) gene expression. Dinoprostone 89-107 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 18772138-2 2008 We have previously shown that in human T lymphocytes the CHOP phosphorylation induced by prostaglandin E(2) (PGE(2))-increased interleukin-8 (IL-8) gene expression. Dinoprostone 89-107 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 18772138-2 2008 We have previously shown that in human T lymphocytes the CHOP phosphorylation induced by prostaglandin E(2) (PGE(2))-increased interleukin-8 (IL-8) gene expression. Prostaglandins E 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 18772138-2 2008 We have previously shown that in human T lymphocytes the CHOP phosphorylation induced by prostaglandin E(2) (PGE(2))-increased interleukin-8 (IL-8) gene expression. Prostaglandins E 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 18772138-3 2008 Given the CHOP positive role in the regulation of transcription, here we have investigated the molecular mechanism(s) by which CHOP increases IL-8 gene activity under PGE(2) stimulus. Prostaglandins E 167-170 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 18772138-5 2008 CHOP silencing confirmed its role in the IL-8 transcriptional regulation and protein production, whereas c-Jun small interfering RNA experiments showed that the PGE(2)-induced activation of IL-8 promoter is mainly c-Jun-independent. Prostaglandins E 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 18772138-6 2008 Moreover, PGE(2) induced CHOP-DNA complexes only when the entire IL-8/AP-1 promoter or the wild type sequences encompassing the AP-1 upstream region were employed. Prostaglandins E 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 18772138-8 2008 The IL-8/AP-1 mutant promoter lacking the sequence immediately upstream the AP-1 site is PGE(2)-unresponsive. Dinoprostone 89-95 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 18772138-9 2008 Finally, chromatin immunoprecipitation data confirmed in vivo that PGE(2) induces CHOP binding to the IL-8 promoter. Dinoprostone 67-73 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 18772138-10 2008 Taken together, our results suggest that the increased expression of CHOP in response to PGE(2) exerts a positive transcriptional regulation of the IL-8 promoter mediated by direct binding to a novel consensus site. Prostaglandins E 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 18713747-3 2008 Here we show that that ecto-nucleoside triphosphate diphosphohydrolase 1 (E-NTPDase1, CD39) is a critical enzyme for hydrolysis of released ATP by neutrophils and for cell migration in response to multiple agonists (N-formyl-methionyl-leucyl-phenylalanine, interleukin-8, and C5a). Adenosine Triphosphate 140-143 C-X-C motif chemokine ligand 8 Homo sapiens 257-270 18692129-7 2008 The data indicate that activation of JNK1/AP-1 and subsequent IL-8 induction in hyperoxia are mediated by intracellular ROS, with SOD having significant protective effects. Reactive Oxygen Species 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 18675368-9 2008 So echinomycin-induced apoptosis in HT-29 cells occurs via NF-kappaB activation independent of caspase-3 activation modulating the resultant-linked key chemokine IL-8 expression and echinomycin-induced apoptosis is NF-kappaB-dependant and directly related to NF-kappaB activation, consequently regulating IL-8 expression. Echinomycin 3-14 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 18675302-6 2008 Moreover, NOS inhibitor (L-NAME) and anti-TLR 4mAb reduced the LPS-induced NO, IL-8 and VEGF production and ICAM-1 expression. NG-Nitroarginine Methyl Ester 25-31 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 18837496-10 2008 The hydration number N h and the dielectric relaxation property of the hydration layer for each salt solution was successfully determined as ( f c1, delta 1, N h)= (18.7, 44.9, 27.9) for NaCl and ( f c1, delta 1, f c2, delta 2, N h) = (26.0, 6.70, 5.64, 19.2) for NaF. Salts 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 264-267 18837496-10 2008 The hydration number N h and the dielectric relaxation property of the hydration layer for each salt solution was successfully determined as ( f c1, delta 1, N h)= (18.7, 44.9, 27.9) for NaCl and ( f c1, delta 1, f c2, delta 2, N h) = (26.0, 6.70, 5.64, 19.2) for NaF. Sodium Chloride 187-191 C-X-C motif chemokine ligand 8 Homo sapiens 264-267 18767879-2 2008 The experimental results indicate that addition of NaF, NaCl, NaHCO 3, or NaNO 3 can result in phase inversion of ATPS-C formed by 12-3-12/AS systems; however, addition of NaBr cannot lead to phase inversion. atps-c 114-120 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 18767879-2 2008 The experimental results indicate that addition of NaF, NaCl, NaHCO 3, or NaNO 3 can result in phase inversion of ATPS-C formed by 12-3-12/AS systems; however, addition of NaBr cannot lead to phase inversion. Arsenic 139-141 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 18767879-5 2008 Phase composition analysis results illustrate that for the ATPS-C formed by 0.10 mol.kg (-1) 12-3-12/AS mixed system, the concentration of Br (-) counterions in the dilute phase of ATPS-C increases with addition of NaF, NaCl, NaHCO 3, or NaNO 3. atps-c 59-65 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 18767879-5 2008 Phase composition analysis results illustrate that for the ATPS-C formed by 0.10 mol.kg (-1) 12-3-12/AS mixed system, the concentration of Br (-) counterions in the dilute phase of ATPS-C increases with addition of NaF, NaCl, NaHCO 3, or NaNO 3. atps-c 181-187 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 18767879-5 2008 Phase composition analysis results illustrate that for the ATPS-C formed by 0.10 mol.kg (-1) 12-3-12/AS mixed system, the concentration of Br (-) counterions in the dilute phase of ATPS-C increases with addition of NaF, NaCl, NaHCO 3, or NaNO 3. Sodium Chloride 220-224 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 18767879-5 2008 Phase composition analysis results illustrate that for the ATPS-C formed by 0.10 mol.kg (-1) 12-3-12/AS mixed system, the concentration of Br (-) counterions in the dilute phase of ATPS-C increases with addition of NaF, NaCl, NaHCO 3, or NaNO 3. nahco 226-231 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 18767879-9 2008 Density experiments illustrate that the density increase of the dilute phase is larger than that of the concentrated phase in the ATPS-C with addition of NaF, NaCl, NaHCO 3, or NaNO 3; thus, phase inversion occurs. atps-c 130-136 C-X-C motif chemokine ligand 8 Homo sapiens 154-157 18675368-0 2008 NF-kappaB-dependency and consequent regulation of IL-8 in echinomycin-induced apoptosis of HT-29 colon cancer cells. Echinomycin 58-69 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 18675368-6 2008 To clarify the role of NF-kappaB on IL-8 expression in echinomycin-mediated apoptosis of HT-29 cells, ELISA plus RT-PCR clearly showed that IL-8 production is inducible by echinomycin treatment. Echinomycin 55-66 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 18675368-6 2008 To clarify the role of NF-kappaB on IL-8 expression in echinomycin-mediated apoptosis of HT-29 cells, ELISA plus RT-PCR clearly showed that IL-8 production is inducible by echinomycin treatment. Echinomycin 55-66 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 18675368-6 2008 To clarify the role of NF-kappaB on IL-8 expression in echinomycin-mediated apoptosis of HT-29 cells, ELISA plus RT-PCR clearly showed that IL-8 production is inducible by echinomycin treatment. Echinomycin 172-183 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 18675368-7 2008 Using a specific inhibitor, IL-8 regulation at echinomycin treatment in HT-29 cells occurred via both caspase-3 and NF-kappaB-dependent signal pathway. Echinomycin 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 18789871-3 2008 Incubation of monocytes with insulin for 2h induced CXCL8 mRNA and secretion whereas glucose had no effect. Deuterium 41-43 C-X-C motif chemokine ligand 8 Homo sapiens 52-57 19046206-1 2008 AIMS: To measure capillary permeability, assessed by skin capillary sodium fluorescein (NaF) leakage, in patients with diabetes mellitus with critical limb ischaemia (DM-CLI) and to compare the effects of vascular endothelial growth factor (VEGF) with those of placebo. Fluorescein 68-86 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 18789871-5 2008 In contrast, blockage of the ERK-specific MAP kinase MEK with PD98059, that prevents phosphorylation of ERK1/ERK2, abrogated insulin-induced CXCL8 release in primary monocytes. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 141-146 18789871-1 2008 Oral glucose uptake alters the function of immune cells and an elevation of systemic CXCL8 was described. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 85-90 18789871-2 2008 Monocytes secrete high amounts of CXCL8 and therefore it was analyzed whether glucose or insulin upregulate monocytic CXCL8 release. Glucose 78-85 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 18789871-7 2008 CXCL8 was also higher when determined in the cell lysate of leukocytes 2h after glucose uptake whereas plasma CXCL8 levels were significantly reduced. Deuterium 71-73 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 18789871-7 2008 CXCL8 was also higher when determined in the cell lysate of leukocytes 2h after glucose uptake whereas plasma CXCL8 levels were significantly reduced. Glucose 80-87 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 18789871-8 2008 In summary, these data indicate that oral glucose uptake in insulin-sensitive adults is associated with elevated monocytic and reduced systemic CXCL8. Glucose 42-49 C-X-C motif chemokine ligand 8 Homo sapiens 144-149 18644822-9 2008 Steroids reduced inflammatory mediators (IL-6, IL-8 and CRP) and neutrophil activation whilst maintaining neutrophil phagocytic functions. Steroids 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 47-59 18506470-10 2008 Inhibition of IL-8 expression by SP600125 suggests that JNK is involved in regulation of proinflammatory mediators of endometrium. pyrazolanthrone 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 18644884-9 2008 The ability of the supernatant to induce IL-8 secretion was reduced by flagellum and cytolethal distending toxin (CDT) gene mutants, treatment of the supernatant with protease K or heat, or treatment of T84 cells with the Toll-like receptor (TLR) inhibitor MyD88 inhibitory peptide or chloroquine. Chloroquine 285-296 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 18662984-2 2008 In this study, we demonstrate that inhibition of PI3K by wortmannin in neutrophil-like differentiated HL60 cells expressing CXCR2 resulted in reduced cell motility but normal chemotaxis in response to a gradient of CXCL8. Wortmannin 57-67 C-X-C motif chemokine ligand 8 Homo sapiens 215-220 19377236-4 2008 The ratios of urinary IL-8 to creatinine (IL-8/C) before and after the treatment were compared with each other. Creatinine 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 42-48 18664535-10 2008 Glucose-induced IL-1beta was biologically active and stimulated IL-8 release. Glucose 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 18565136-0 2008 Irsogladine maleate abolishes the increase in interleukin-8 levels caused by outer membrane protein 29 from Aggregatibacter (Actinobacillus) actinomycetemcomitans through the ERK pathway in human gingival epithelial cells. irsogladine 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 18565136-1 2008 BACKGROUND AND OBJECTIVE: Irsogladine maleate (IM) suppresses the increase in interleukin (IL)-8 production induced by outer membrane protein (OMP) 29 from Aggregatibacter (Actinobacillus) actinomycetemcomitans in cultures of human gingival epithelial cells (HGEC). irsogladine 26-45 C-X-C motif chemokine ligand 8 Homo sapiens 78-96 18565136-7 2008 RESULTS: An ERK inhibitor, PD98059, as well as IM, obviated the OMP29-induced increase in IL-8 levels in HGEC. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 18282785-4 2008 Overexpression of CXCL8 in HN4 primary tumor cells with low endogenous CXCL8 levels was found to increase cell growth, as judged by cell counting and MTT assays. monooxyethylene trimethylolpropane tristearate 150-153 C-X-C motif chemokine ligand 8 Homo sapiens 18-23 18974961-4 2008 To investigate the role of ROS in pathogenesis of periodontitis, we estimated the effect of H(2)O(2), one of ROS, on the expression of IL-8 in human periodontal ligament (PDL) cells. Reactive Oxygen Species 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 18974961-4 2008 To investigate the role of ROS in pathogenesis of periodontitis, we estimated the effect of H(2)O(2), one of ROS, on the expression of IL-8 in human periodontal ligament (PDL) cells. Reactive Oxygen Species 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 18974961-8 2008 Treatment with H(2)O(2) at concentration of up to 250 microM increased IL-8 mRNA expression and production in a concentration-dependent manner. Hydrogen Peroxide 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 18974961-10 2008 Catalase, an inhibitor of H(2)O(2), down-regulated the production of IL-8 induced by H(2)O(2). Water 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 18974961-10 2008 Catalase, an inhibitor of H(2)O(2), down-regulated the production of IL-8 induced by H(2)O(2). Water 85-90 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 18974961-12 2008 Pretreatment with PD98059 (ERK inhibitor), SB203580 (p38 inhibitor), or SP600125 (JNK inhibitor) decreased the IL-8 production induced by H(2)O(2). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 18974961-12 2008 Pretreatment with PD98059 (ERK inhibitor), SB203580 (p38 inhibitor), or SP600125 (JNK inhibitor) decreased the IL-8 production induced by H(2)O(2). SB 203580 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 18974961-12 2008 Pretreatment with PD98059 (ERK inhibitor), SB203580 (p38 inhibitor), or SP600125 (JNK inhibitor) decreased the IL-8 production induced by H(2)O(2). pyrazolanthrone 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 18974961-13 2008 These results indicate that H(2)O(2) acts as an inducer of IL-8 secretion via activation of ERK, p38, and JNK in PDL cells. Hydrogen Peroxide 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 18662984-3 2008 However, wortmannin inhibition of PI3K did impair the ability of cells to re-orient their polarity and respond quickly to a change in the direction of the CXCL8 gradient. Wortmannin 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 155-160 18662758-4 2008 The results show that H(2)O(2) and quartz exposure induced almost identical levels of CXCL8 (interleukin-8) release in the alveolar epithelial cell line A549, but in the bronchial epithelial cell line BEAS-2B, H(2)O(2)-exposure did not affect CXCL8 release significantly, whereas quartz induced a 16-fold increase. Hydrogen Peroxide 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 86-91 18662758-4 2008 The results show that H(2)O(2) and quartz exposure induced almost identical levels of CXCL8 (interleukin-8) release in the alveolar epithelial cell line A549, but in the bronchial epithelial cell line BEAS-2B, H(2)O(2)-exposure did not affect CXCL8 release significantly, whereas quartz induced a 16-fold increase. Hydrogen Peroxide 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 93-106 18662758-4 2008 The results show that H(2)O(2) and quartz exposure induced almost identical levels of CXCL8 (interleukin-8) release in the alveolar epithelial cell line A549, but in the bronchial epithelial cell line BEAS-2B, H(2)O(2)-exposure did not affect CXCL8 release significantly, whereas quartz induced a 16-fold increase. Hydrogen Peroxide 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 243-248 18615482-7 2008 RESULTS: Selective zinc deficiency induced by the membrane-permeable zinc chelator N,N,N",N"-tetrakis(2-pyridylmethyl)-ethylenediamine (TPEN) increases activation of NF-kappaB and up-regulates expression of the NF-kappaB controlled pro-angiogenic and pro-metastatic cytokines VEGF, IL-6 and IL-8 in androgen-independent PC-3 and DU-145 prostate cancer cells. N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine 136-140 C-X-C motif chemokine ligand 8 Homo sapiens 291-295 18586957-3 2008 IL-1beta-induced IL-8 release was also repressed by PGE(2) and forskolin, whereas the beta(2)-adrenoceptor agonists were ineffective. Prostaglandins E 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 18599499-0 2008 Double-stranded RNA-activated protein kinase mediates induction of interleukin-8 expression by deoxynivalenol, Shiga toxin 1, and ricin in monocytes. deoxynivalenol 95-109 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 18599499-5 2008 Preincubation of human monocytic U937 cells with the PKR inhibitors C16 and 2-aminopurine (2-AP) blocked DON-induced expression of IL-8 protein and mRNA. Palmitic Acid 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 18599499-5 2008 Preincubation of human monocytic U937 cells with the PKR inhibitors C16 and 2-aminopurine (2-AP) blocked DON-induced expression of IL-8 protein and mRNA. 2-Aminopurine 76-89 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 18599499-5 2008 Preincubation of human monocytic U937 cells with the PKR inhibitors C16 and 2-aminopurine (2-AP) blocked DON-induced expression of IL-8 protein and mRNA. 2-Aminopurine 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 18599499-5 2008 Preincubation of human monocytic U937 cells with the PKR inhibitors C16 and 2-aminopurine (2-AP) blocked DON-induced expression of IL-8 protein and mRNA. deoxynivalenol 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 18599499-7 2008 Nuclear factor-kappa B binding, which has been previously shown to be a requisite for DON-induced IL-8 transcription, was markedly reduced in UK9M cells as compared with UK9C cells. deoxynivalenol 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 18599499-8 2008 As observed for DON, ricin-, and Stx1-induced IL-8 expression was suppressed by the PKR inhibitors C16 and 2-AP as well as impaired in UK9M cells. deoxynivalenol 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 18599499-8 2008 As observed for DON, ricin-, and Stx1-induced IL-8 expression was suppressed by the PKR inhibitors C16 and 2-AP as well as impaired in UK9M cells. 2-Aminopurine 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 18599499-9 2008 Taken together, these data indicate that PKR plays a common role in IL-8 induction by DON and the two RIPs, suggesting that this kinase might be a critical factor in RSR. deoxynivalenol 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 18403779-10 2008 AG1478 (EGFR inhibitor) restored normal TLR4/2 levels and also suppressed synergistic release of IL-8. RTKI cpd 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 18926057-3 2008 The aim of this study was to investigate the effects of these two antihistamines (cetirizine and levocetirizine) on granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin (IL)-8 secretion in A549 human airway epithelial cells. Cetirizine 82-92 C-X-C motif chemokine ligand 8 Homo sapiens 178-196 18926057-3 2008 The aim of this study was to investigate the effects of these two antihistamines (cetirizine and levocetirizine) on granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin (IL)-8 secretion in A549 human airway epithelial cells. levocetirizine 97-111 C-X-C motif chemokine ligand 8 Homo sapiens 178-196 18926057-7 2008 Cetirizine (10 microM) and levocetirizine (5 and 10 microM) significantly suppressed IL-8 secretion after A549 was stimulated. Cetirizine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 18926057-7 2008 Cetirizine (10 microM) and levocetirizine (5 and 10 microM) significantly suppressed IL-8 secretion after A549 was stimulated. levocetirizine 27-41 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 18926057-9 2008 Moreover, levocetirizine, 5 microM, was better than cetirizine, 5 microM, on suppressing IL-8 secretion, but such a difference did not appear in other conditions. levocetirizine 10-24 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 18926057-9 2008 Moreover, levocetirizine, 5 microM, was better than cetirizine, 5 microM, on suppressing IL-8 secretion, but such a difference did not appear in other conditions. Cetirizine 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 18586957-3 2008 IL-1beta-induced IL-8 release was also repressed by PGE(2) and forskolin, whereas the beta(2)-adrenoceptor agonists were ineffective. Colforsin 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 18926057-10 2008 Our results suggest that cetirizine and levocetirizine at higher concentrations can reduce the release of GM-CSF and IL-8 from A549 cells stimulated with IL-1beta. Cetirizine 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 18926057-10 2008 Our results suggest that cetirizine and levocetirizine at higher concentrations can reduce the release of GM-CSF and IL-8 from A549 cells stimulated with IL-1beta. levocetirizine 40-54 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 18765195-10 2008 BAL IL-8 levels were higher in the SAL-3 group compared with the PER-3 group. sal 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 18377686-8 2008 Ellagic acid, genistein and epigallocatechin gallate reduced (4- to 8-fold) IL-1beta-induced IL-8 secretion, while resveratrol promoted (1.7-fold) the secretion. Ellagic Acid 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 18377686-8 2008 Ellagic acid, genistein and epigallocatechin gallate reduced (4- to 8-fold) IL-1beta-induced IL-8 secretion, while resveratrol promoted (1.7-fold) the secretion. Genistein 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 18377686-8 2008 Ellagic acid, genistein and epigallocatechin gallate reduced (4- to 8-fold) IL-1beta-induced IL-8 secretion, while resveratrol promoted (1.7-fold) the secretion. epigallocatechin gallate 28-52 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 18841306-13 2008 In an assay to determine inhibition of the H2O2-activated release of PGE2, IL-6, and IL-8 in human normal fibroblast cell lines, the release of PGE2 and IL-6 was almost completely inhibited above concentrations of 0.05% and 1%, respectively. Hydrogen Peroxide 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 18841306-13 2008 In an assay to determine inhibition of the H2O2-activated release of PGE2, IL-6, and IL-8 in human normal fibroblast cell lines, the release of PGE2 and IL-6 was almost completely inhibited above concentrations of 0.05% and 1%, respectively. Dinoprostone 144-148 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 18786233-11 2008 Our findings demonstrate the IL23/IL17 axis to be involved in the pathophysiology of BOS potentially triggering the IL8-mediated neutrophilia. N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 18506912-0 2008 Changes in IL-8 release and intracellular content in DMSO-differentiated HL-60 cells after treatment with 4-hydroxynonenal. Dimethyl Sulfoxide 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 18506912-0 2008 Changes in IL-8 release and intracellular content in DMSO-differentiated HL-60 cells after treatment with 4-hydroxynonenal. 4-hydroxy-2-nonenal 106-122 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 18506912-2 2008 In this work we studied HNE effects on the intracellular content of IL-8 and its release in DMSO-differentiated HL-60 cells. Dimethyl Sulfoxide 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 18506912-5 2008 The addition of 0.1 microM IL-8 to DMSO-differentiated HL-60 cells induced a strong increase of exocytosis, measured by beta-glucuronidase secretion. Dimethyl Sulfoxide 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 18341570-0 2008 Tetracycline suppresses ATP gamma S-induced CXCL8 and CXCL1 production by the human dermal microvascular endothelial cell-1 (HMEC-1) cell line and primary human dermal microvascular endothelial cells. Tetracycline 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 44-49 18341570-0 2008 Tetracycline suppresses ATP gamma S-induced CXCL8 and CXCL1 production by the human dermal microvascular endothelial cell-1 (HMEC-1) cell line and primary human dermal microvascular endothelial cells. adenosine 5'-O-(3-thiotriphosphate) 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 44-49 18341570-6 2008 TCN dose-dependently inhibited ATP gamma S-induced augmentation of CXCL8 (interleukin-8) and CXCL1 (growth-regulated oncogene-alpha) production by HMEC-1 cells and primary human dermal endothelial cells in vitro. Tetracyclines 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 67-72 18341570-6 2008 TCN dose-dependently inhibited ATP gamma S-induced augmentation of CXCL8 (interleukin-8) and CXCL1 (growth-regulated oncogene-alpha) production by HMEC-1 cells and primary human dermal endothelial cells in vitro. Tetracyclines 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 18341570-6 2008 TCN dose-dependently inhibited ATP gamma S-induced augmentation of CXCL8 (interleukin-8) and CXCL1 (growth-regulated oncogene-alpha) production by HMEC-1 cells and primary human dermal endothelial cells in vitro. adenosine 5'-O-(3-thiotriphosphate) 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 67-72 18341570-6 2008 TCN dose-dependently inhibited ATP gamma S-induced augmentation of CXCL8 (interleukin-8) and CXCL1 (growth-regulated oncogene-alpha) production by HMEC-1 cells and primary human dermal endothelial cells in vitro. adenosine 5'-O-(3-thiotriphosphate) 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 18613793-8 2008 In addition, compared with the CP group, in the CTU group the balance between proinflammatory mediators (such as tumor necrosis factor-alpha, interleukin [IL]-1beta, IL-6, and IL-8) and anti-inflammatory cytokines (including IL-4 and IL-10) was better modulated, and the cumulative survival rate of the CTU group exceeded that of the CP group by 17.8% at day 28, 25.9% at day 60, and 27.4% at day 90. 3,9-Bis(2-cyanoethyl)-2,4,8,10-tetraoxaspiro[5.5]undecane 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 18768046-11 2008 Lung tissue homogenate in the methylprednisolone group had lower levels of TNF-alpha (P < 0.05), IL-1beta (P < 0.05), and IL-8 (P < 0.05) in both the collapsed and the ventilated lungs. Methylprednisolone 30-48 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 18574003-3 2008 This 4-PBA-induced IL-8 production was associated with a strong reduction of proteasome and nuclear factor-kappaB transcriptional activities in the two DeltaF508-CFTR lung cells either in a resting state or after tumor necrosis factor-alpha stimulation. 4-phenylbutyric acid 5-10 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 18574003-7 2008 Therefore, we suggest that inhibition of both ERK1/2 and JNK signaling may be a means to strongly reduce 4-PBA-induced IL-8 production in combination with 4-PBA treatment to restore CFTR Cl(-) channel function in lung epithelial cells of patients with CF. 4-phenylbutyric acid 105-110 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 18790747-5 2008 Pretreatment with the CXCR2 antagonist AZ10397767 significantly attenuated IL-8-induced c-FLIP mRNA up-regulation whereas inhibition of androgen receptor- and/or nuclear factor-kappaB-mediated transcription attenuated IL-8-induced c-FLIP expression in LNCaP and PC3 cells, respectively. AZ10397767 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 18600309-0 2008 Salmeterol with fluticasone enhances the suppression of IL-8 release and increases the translocation of glucocorticoid receptor by human neutrophils stimulated with cigarette smoke. Salmeterol Xinafoate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 18600309-0 2008 Salmeterol with fluticasone enhances the suppression of IL-8 release and increases the translocation of glucocorticoid receptor by human neutrophils stimulated with cigarette smoke. Fluticasone 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 18600309-2 2008 Recently, we have demonstrated that combination of salmeterol and fluticasone propionate (FP) additionally suppress the production of IL-8 by human monocyte. Salmeterol Xinafoate 51-61 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 18600309-2 2008 Recently, we have demonstrated that combination of salmeterol and fluticasone propionate (FP) additionally suppress the production of IL-8 by human monocyte. Fluticasone 66-88 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 18600309-6 2008 Cigarette smoke medium (CSM) induces an increased expression of CXC receptors and the production of ROS that may explain the strong production of IL-8 by neutrophils. Reactive Oxygen Species 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 18493738-9 2008 RESULTS: Physiological concentrations of C-peptide affect high glucose-induced endothelial dysfunction by: (1) decreasing VCAM-1 expression and U-937 cell adherence to HAEC; (2) reducing secretion of IL-8 and MCP-1; and (3) suppressing NF-kappaB activation. Glucose 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 18617548-9 2008 TCDD up-regulated the expression of IL-1beta, IL-6 and IL-8 through binding to AhR, and this effect was transmitted via the NF-kappaB and ERK signalling cascades. Polychlorinated Dibenzodioxins 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 18662754-6 2008 The induction of IL-8 by titanium dioxide nanoparticles was inhibited by the pre-treatment with SB203580 and PD98059, which means that the IL-8 was induced through p38 mitogen-activated protein kinase (MAPK) pathway and/or extracellular signal (ERK) pathway. titanium dioxide 25-41 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 18662754-6 2008 The induction of IL-8 by titanium dioxide nanoparticles was inhibited by the pre-treatment with SB203580 and PD98059, which means that the IL-8 was induced through p38 mitogen-activated protein kinase (MAPK) pathway and/or extracellular signal (ERK) pathway. titanium dioxide 25-41 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 18662754-6 2008 The induction of IL-8 by titanium dioxide nanoparticles was inhibited by the pre-treatment with SB203580 and PD98059, which means that the IL-8 was induced through p38 mitogen-activated protein kinase (MAPK) pathway and/or extracellular signal (ERK) pathway. SB 203580 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 18662754-6 2008 The induction of IL-8 by titanium dioxide nanoparticles was inhibited by the pre-treatment with SB203580 and PD98059, which means that the IL-8 was induced through p38 mitogen-activated protein kinase (MAPK) pathway and/or extracellular signal (ERK) pathway. SB 203580 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 18662754-6 2008 The induction of IL-8 by titanium dioxide nanoparticles was inhibited by the pre-treatment with SB203580 and PD98059, which means that the IL-8 was induced through p38 mitogen-activated protein kinase (MAPK) pathway and/or extracellular signal (ERK) pathway. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 109-116 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 18662754-6 2008 The induction of IL-8 by titanium dioxide nanoparticles was inhibited by the pre-treatment with SB203580 and PD98059, which means that the IL-8 was induced through p38 mitogen-activated protein kinase (MAPK) pathway and/or extracellular signal (ERK) pathway. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 109-116 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 18501560-5 2008 Leptin-mediated IL-8 production was attenuated by OBRl receptor antisense oligonucleotide, JAK2 inhibitor or STAT3 small interference RNA (siRNA). Oligonucleotides 74-89 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 18501560-8 2008 Moreover, pretreatment with p300 inhibitor (curcumin) also blocked IL-8 expression. Curcumin 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 18501560-9 2008 The binding of p65 to the NF-kappaB elements, as well as the recruitment of p300 and the enhancement of histone H3 acetylation on the IL-8 promoter was enhanced by leptin, which was inhibited by wortmannin, Akt inhibitor or IRS-1 siRNA. Wortmannin 195-205 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 18688536-3 2008 Quantitative polarization analysis of the measured SHG data indicated that the average orientation of the interfacial water molecules changed only slightly around 40 degrees with the increase of the bulk concentration of the three sodium halides, namely NaF, NaCl and NaBr, from that of the neat air/water interface. Water 118-123 C-X-C motif chemokine ligand 8 Homo sapiens 254-257 18688536-3 2008 Quantitative polarization analysis of the measured SHG data indicated that the average orientation of the interfacial water molecules changed only slightly around 40 degrees with the increase of the bulk concentration of the three sodium halides, namely NaF, NaCl and NaBr, from that of the neat air/water interface. sodium halides 231-245 C-X-C motif chemokine ligand 8 Homo sapiens 254-257 18688536-4 2008 The observed significant SHG signal increase with the bulk salt concentration is attributed to the overall increase of the thickness of the interfacial water molecular layer, following the order of NaBr > NaCl approximately NaF. Salts 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 227-230 18688536-4 2008 The observed significant SHG signal increase with the bulk salt concentration is attributed to the overall increase of the thickness of the interfacial water molecular layer, following the order of NaBr > NaCl approximately NaF. Water 152-157 C-X-C motif chemokine ligand 8 Homo sapiens 227-230 18485432-0 2008 Hypo-responsiveness of interleukin-8 production in human embryonic epithelial intestine 407 cells independent of NF-kappaB pathway: new lessons from endotoxin and ribotoxic deoxynivalenol. deoxynivalenol 173-187 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 18485432-4 2008 Taking the knowledge into consideration, we tested the hypothesis that endotoxin pre-exposure can attenuate ribotoxin-induced epithelial interleukin-8 (IL-8) production via a tolerance mechanism. ribotoxin 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 137-150 18485432-4 2008 Taking the knowledge into consideration, we tested the hypothesis that endotoxin pre-exposure can attenuate ribotoxin-induced epithelial interleukin-8 (IL-8) production via a tolerance mechanism. ribotoxin 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 18660424-9 2008 Poly(I:C)-induced expression of IL-6, IL-8, G-CSF, MIP-1beta, exotaxin, RANTES, and ICAM-1 was inhibited differentially by the MAPK inhibitors PD98059 and SB203580 and by JNK inhibitor II. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 18636175-0 2008 Glucosamine suppresses interleukin-8 production and ICAM-1 expression by TNF-alpha-stimulated human colonic epithelial HT-29 cells. Glucosamine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 18636175-4 2008 The results revealed that glucosamine suppressed the IL-8 production and ICAM-1 expression by TNF-alpha-activated HT-29 cells. Glucosamine 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 18636175-6 2008 Thus, glucosamine demonstrates inhibitory actions on the inflammatory and signaling molecules (IL-8, ICAM-1, p38MAPK and NF-kappaB) in intestinal epithelial cells. Glucosamine 6-17 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 18664347-11 2008 The change of IL-8 level before and after treatment in Tanreqing group was greater than that in ambroxol hydrochloride group and the control group. Ambroxol 96-118 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 18729741-4 2008 Cycloheximide treatment indicated that the augmenting effect of CSC on IL-1alpha, IL-1beta and IL-8, but not IL-6 and CYP1A1, mRNA expression requires de novo protein synthesis. Cycloheximide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 18660424-7 2008 RESULTS: Poly(I:C) induced the up-regulation of TLR3, the release of IL-6, IL-8, G-CSF, MIP-1beta, eotaxin, and RANTES, and the expression of ICAM-1 and VCAM-1 in corneal fibroblasts. Poly I-C 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 18656796-7 2008 Furthermore, bile acid levels, but not pepsin levels, correlated positively with BAL neutrophilia and IL-8 protein levels. Bile Acids and Salts 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 18656796-9 2008 This relationship between reflux and airway colonization and their role in the development of chronic allograft dysfunction/BOS after LTx should be further elucidated; nevertheless, induction of IL-8-mediated neutrophilic airway inflammation may be a putative mechanism. Leukotriene C4 134-137 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 19967052-5 2008 HSP22-induced IL-8 release was inhibited by U0126, but not by SB202190. U 0126 44-49 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 18074179-10 2008 RESULTS: Exposure to 100% CO(2) completely blocked spontaneous and IL-8 induced migration of PMNs (p < 0.001 vs. controls). Carbon Dioxide 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 18508130-1 2008 The chemokine interleukin 8/CXCL8 induces the phosphorylation of the GluR1 subunit of the AMPA-type glutamate receptor in neurons and transfected HEK cells, on both serine 845 (S845) and 831 (S831) residues. Serine 165-171 C-X-C motif chemokine ligand 8 Homo sapiens 28-33 18502748-5 2008 We found that exposure of RPE cells to H(2)O(2), paraquat, or A2E-mediated photooxidation resulted in increased expression and secretion of IL-8. Paraquat 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 18655734-14 2008 After immersion in the NaF solution, fluoride concentrations at the surfaces of the disks increased when compared with previous storage media (FT>FVIII>KN>FII>FIX). Fluorides 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 18487355-14 2008 Whereas clarithromycin, azithromycin, and moxifloxacin individually were able to inhibit TNF-alpha-induction of IL-8, each failed to inhibit MMF-induction of IL-8. Clarithromycin 8-22 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 18571505-5 2008 Adding AG1296 with RA increased secretion of TNF-alpha, IL-8, and MMP-9 expression. 6,7-dimethoxy-3-phenylquinoxaline 7-13 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 18571505-5 2008 Adding AG1296 with RA increased secretion of TNF-alpha, IL-8, and MMP-9 expression. Tretinoin 19-21 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 18468509-3 2008 Additionally, rhLIGHT was found to increase ROS via NADPH oxidase p47(phox) phosphorylation, which was found to be required for LIGHT-induced NF-kappaB activation, CCR1 and CCR2 expression, migration and IL-8 and TNF-alpha production. Reactive Oxygen Species 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 18487355-14 2008 Whereas clarithromycin, azithromycin, and moxifloxacin individually were able to inhibit TNF-alpha-induction of IL-8, each failed to inhibit MMF-induction of IL-8. Azithromycin 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 18487355-14 2008 Whereas clarithromycin, azithromycin, and moxifloxacin individually were able to inhibit TNF-alpha-induction of IL-8, each failed to inhibit MMF-induction of IL-8. Moxifloxacin 42-54 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 18607537-7 2008 An IkappaB kinase 2 inhibitor, sc514, also strongly reduced IL-8 and significantly induced p53 protein levels. SC 514 31-36 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 18580215-10 2008 Significant increases in systemic IL-6 and IL-8 values were measured only in patients undergoing DAP and SP. dap 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 18580215-10 2008 Significant increases in systemic IL-6 and IL-8 values were measured only in patients undergoing DAP and SP. TFF2 protein, human 105-107 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 18500358-9 2008 KEY RESULTS: EtP was several-fold more potent than EtOH in reducing adhesion of neutrophils to activated HUVECs, generation of IL-8 or G-CSF and surface expression of the adhesion molecules. ethyl pyruvate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 18506884-6 2008 The mutually antagonistic relationship between IFN-gamma and PGE(2) extends to downstream cytokine and chemokine release; PGE(2) counters the effects of IFN-gamma, on the release of IP-10, IL-8, TNF-alpha and IL-1beta. Prostaglandins E 122-125 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 18452717-6 2008 The combination of ROS quenching by the free radical scavenger Tempol and of Bcl10 silencing by siRNA completely inhibited the CGN-induced increases in nuclear NFkappaB (p65), phospho-IkappaBalpha, and secretion of IL-8. Reactive Oxygen Species 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 18275043-11 2008 However, OGM-differentiated hMSCs showed an increase in CXCL8 levels when treated with the NF-kappaB inhibitor PDTC, a pyrrolidine derivative of dithiocarbamate. pyrrolidine 119-130 C-X-C motif chemokine ligand 8 Homo sapiens 56-61 18275043-11 2008 However, OGM-differentiated hMSCs showed an increase in CXCL8 levels when treated with the NF-kappaB inhibitor PDTC, a pyrrolidine derivative of dithiocarbamate. Dithiocarbamate 145-160 C-X-C motif chemokine ligand 8 Homo sapiens 56-61 18311596-2 2008 Here we demonstrate that cholesterol was absolutely required for polarized redistribution of key chemotactic mediators in human neutrophils in response to all chemoattractants tested (fMet-Leu-Phe, and the chemokines CXCL1, CXCL8 and CXCL12). Cholesterol 25-36 C-X-C motif chemokine ligand 8 Homo sapiens 224-229 18566387-9 2008 cis-UCA also increased cytokine protein production such as that of TNF-alpha, IL-6, and IL-8 in a dose-dependent manner. cis-Urocanic acid 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 19079193-7 2008 Estradiol also reversed the stimulatory effects of IL-1beta on mRNA expression of TNF-alpha, IL-8, and NF-kB by 85, 95, and 70%, respectively. Estradiol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 18830893-5 2008 PAH induced significant secretion of IL-1beta, IL-8, and IL-12 after 24 or 48 hr of treatment, an effect reinforced by LPS stimulation; no effect on IL-10 secretion was noted. Polycyclic Aromatic Hydrocarbons 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 18603066-7 2008 RESULTS: Four-hour pretreatment markedly reduced inflammatory endothelial release of interleukin 8 (2587 +/- 82 pg/mL control vs 208 +/- 3 pg/mL omega-3 pretreated, P < .01) and endothelial expression of intercellular adhesion molecule 1 (196.1 +/- 2.0 vs 71.9 +/- 0.6 mean channel fluorescence, P < .01) in response to endotoxin and tumor necrosis factor a. Neutrophil activation (CD11b and respiratory burst) was maintained, but pretreated neutrophils had shorter survival. Fatty Acids, Omega-3 145-152 C-X-C motif chemokine ligand 8 Homo sapiens 85-98 18515093-8 2008 LCA significantly decreased IL-8 secretion induced by IL-1beta. Lithocholic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 114-131 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 114-131 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 114-131 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 114-131 C-X-C motif chemokine ligand 8 Homo sapiens 242-247 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 114-131 C-X-C motif chemokine ligand 8 Homo sapiens 248-252 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 242-247 18533267-5 2008 The generation of interleukin-8 (CXCL8/IL-8) by human DCs conditioned with CSE was suppressed by the anti-oxidant n-acetyl cysteine (NAC), implying the involvement of oxidant sensitive pathways as a primary mechanism involved in the enhanced CXCL8/IL-8 generation. Acetylcysteine 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 248-252 18533267-7 2008 Whereas NAC suppressed production of CXCL8 by CSE-conditioned DCs, it augmented production of PGE2 and cellular COX-2 levels in maturing DCs. Acetylcysteine 8-11 C-X-C motif chemokine ligand 8 Homo sapiens 37-42 21479441-4 2008 EGCG downregulated the levels of pro-inflammatory cytokine interleukin (IL)-6 and chemokines IL-8, monocyte-chemoattractant protein (MCP)-1 and RANTES. epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 18767394-2 2008 LPS-induced IL-8 production in leukocyte fraction was inhibited by beta-endorphin 10(-7), 10(-11) M. The enchasing effect of beta-endorphin on IL-1beta production was not blocked by naloxone and naltrindole. lps 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 18546154-6 2008 DCIP-selective antisense oligodeoxynucleotide inhibited the expression of TNF-alpha-responsive gene targets including vascular cell adhesion molecule-1, intercellular adhesion molecule-1, IL-6, IL-8, IP-10, and thymic stromal lymphopoietin. dcip 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 18546154-6 2008 DCIP-selective antisense oligodeoxynucleotide inhibited the expression of TNF-alpha-responsive gene targets including vascular cell adhesion molecule-1, intercellular adhesion molecule-1, IL-6, IL-8, IP-10, and thymic stromal lymphopoietin. Oligodeoxyribonucleotides 25-45 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 18767394-4 2008 In mononuclear and neutrophile fractions beta-endorphin and delta-agonist DADLE enchased IL-1beta production in spontaneous and LPS-stimulating cultures, when IL-8 production inhibited beta-endorphin and delta-agonist DADLE only in LPS presence. lps 232-235 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 18767394-5 2008 No effect of mu-agonist DAGO were observed on IL-1beta production, whereas LPS-induced IL-8 secretion in neutrophile fraction inhibited by DAGO. lps 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 18767394-2 2008 LPS-induced IL-8 production in leukocyte fraction was inhibited by beta-endorphin 10(-7), 10(-11) M. The enchasing effect of beta-endorphin on IL-1beta production was not blocked by naloxone and naltrindole. Naloxone 182-190 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 18767394-2 2008 LPS-induced IL-8 production in leukocyte fraction was inhibited by beta-endorphin 10(-7), 10(-11) M. The enchasing effect of beta-endorphin on IL-1beta production was not blocked by naloxone and naltrindole. naltrindole 195-206 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 18767394-3 2008 The inhibitory effect of beta-endorphin on IL-8 production was blocked by naloxone and naltrindole. Naloxone 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 18767394-3 2008 The inhibitory effect of beta-endorphin on IL-8 production was blocked by naloxone and naltrindole. naltrindole 87-98 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 18424663-5 2008 CBMCs responded to stimulation with polyinosinic.polycytidylic acid by producing a distinct chemokine profile, including CCL4, CXCL8, and CXCL10. cbmcs 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 127-132 18424663-5 2008 CBMCs responded to stimulation with polyinosinic.polycytidylic acid by producing a distinct chemokine profile, including CCL4, CXCL8, and CXCL10. Poly I-C 36-67 C-X-C motif chemokine ligand 8 Homo sapiens 127-132 18424663-6 2008 CBMCs produced significant amounts of CXCL8 in response to low levels of reovirus infection, while both skin- and lung-derived fibroblasts were unresponsive unless higher doses of reovirus were used. cbmcs 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 18424663-7 2008 Supernatants from CBMCs infected with reovirus induced substantial NK cell chemotaxis that was highly dependent on CXCL8 and CXCR1. cbmcs 18-23 C-X-C motif chemokine ligand 8 Homo sapiens 115-120 18390828-8 2008 IL-8/CXCL8 induction and ERK1/2 activation were preceded by EGF receptor (EGFR) tyrosine phosphorylation, within 2 min, and reduced by selective EGFR tyrosine kinase inhibitors (AG-1478 and PD168393) by a neutralizing EGFR antibody and by small interfering RNA oligonucleotides directed against EGFR, implicating EGFR activation. RTKI cpd 178-185 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18390828-3 2008 Stimulation with rhMMP-12 resulted in a concentration-dependent IL-8/CXCL8 synthesis 6 h later. rhmmp-12 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 18390828-3 2008 Stimulation with rhMMP-12 resulted in a concentration-dependent IL-8/CXCL8 synthesis 6 h later. rhmmp-12 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 69-74 18390828-5 2008 In A549 cells, synthetic matrix metalloproteinase (MMP) inhibitors prevented rhMMP-12-induced IL-8/CXCL8 release. rhmmp-12 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 18390828-5 2008 In A549 cells, synthetic matrix metalloproteinase (MMP) inhibitors prevented rhMMP-12-induced IL-8/CXCL8 release. rhmmp-12 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 18375743-9 2008 We conclude that multiple TLR ligands induce airway epithelial cell production of IL-8 and VEGF via a Duox1--> ROS--> TACE--> TGF-alpha--> EGFR phosphorylation pathway. Reactive Oxygen Species 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 18390828-8 2008 IL-8/CXCL8 induction and ERK1/2 activation were preceded by EGF receptor (EGFR) tyrosine phosphorylation, within 2 min, and reduced by selective EGFR tyrosine kinase inhibitors (AG-1478 and PD168393) by a neutralizing EGFR antibody and by small interfering RNA oligonucleotides directed against EGFR, implicating EGFR activation. RTKI cpd 178-185 C-X-C motif chemokine ligand 8 Homo sapiens 5-10 18390828-7 2008 Selective MEK inhibitors (U0126 and PD-98059) blocked both IL-8/CXCL8 release and ERK1/2 phosphorylation. U 0126 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 18390828-7 2008 Selective MEK inhibitors (U0126 and PD-98059) blocked both IL-8/CXCL8 release and ERK1/2 phosphorylation. U 0126 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 64-69 18390828-8 2008 IL-8/CXCL8 induction and ERK1/2 activation were preceded by EGF receptor (EGFR) tyrosine phosphorylation, within 2 min, and reduced by selective EGFR tyrosine kinase inhibitors (AG-1478 and PD168393) by a neutralizing EGFR antibody and by small interfering RNA oligonucleotides directed against EGFR, implicating EGFR activation. PD168393 190-198 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18390828-7 2008 Selective MEK inhibitors (U0126 and PD-98059) blocked both IL-8/CXCL8 release and ERK1/2 phosphorylation. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 18390828-7 2008 Selective MEK inhibitors (U0126 and PD-98059) blocked both IL-8/CXCL8 release and ERK1/2 phosphorylation. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 64-69 18390828-8 2008 IL-8/CXCL8 induction and ERK1/2 activation were preceded by EGF receptor (EGFR) tyrosine phosphorylation, within 2 min, and reduced by selective EGFR tyrosine kinase inhibitors (AG-1478 and PD168393) by a neutralizing EGFR antibody and by small interfering RNA oligonucleotides directed against EGFR, implicating EGFR activation. PD168393 190-198 C-X-C motif chemokine ligand 8 Homo sapiens 5-10 18390828-8 2008 IL-8/CXCL8 induction and ERK1/2 activation were preceded by EGF receptor (EGFR) tyrosine phosphorylation, within 2 min, and reduced by selective EGFR tyrosine kinase inhibitors (AG-1478 and PD168393) by a neutralizing EGFR antibody and by small interfering RNA oligonucleotides directed against EGFR, implicating EGFR activation. Tyrosine 80-88 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18390828-8 2008 IL-8/CXCL8 induction and ERK1/2 activation were preceded by EGF receptor (EGFR) tyrosine phosphorylation, within 2 min, and reduced by selective EGFR tyrosine kinase inhibitors (AG-1478 and PD168393) by a neutralizing EGFR antibody and by small interfering RNA oligonucleotides directed against EGFR, implicating EGFR activation. Tyrosine 80-88 C-X-C motif chemokine ligand 8 Homo sapiens 5-10 18390828-8 2008 IL-8/CXCL8 induction and ERK1/2 activation were preceded by EGF receptor (EGFR) tyrosine phosphorylation, within 2 min, and reduced by selective EGFR tyrosine kinase inhibitors (AG-1478 and PD168393) by a neutralizing EGFR antibody and by small interfering RNA oligonucleotides directed against EGFR, implicating EGFR activation. Oligonucleotides 261-277 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18390828-8 2008 IL-8/CXCL8 induction and ERK1/2 activation were preceded by EGF receptor (EGFR) tyrosine phosphorylation, within 2 min, and reduced by selective EGFR tyrosine kinase inhibitors (AG-1478 and PD168393) by a neutralizing EGFR antibody and by small interfering RNA oligonucleotides directed against EGFR, implicating EGFR activation. Oligonucleotides 261-277 C-X-C motif chemokine ligand 8 Homo sapiens 5-10 18390828-10 2008 Using small interfering technique, we showed that c-Fos is involved in rhMMP-12-induced IL-8/CXCL8 production. rhmmp-12 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 18390828-10 2008 Using small interfering technique, we showed that c-Fos is involved in rhMMP-12-induced IL-8/CXCL8 production. rhmmp-12 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 93-98 18486963-5 2008 This enhancement is attributed to the formation of complex compounds between EDTA/NaF and reaction products, such as Cr(III) and Fe(III), which eliminate the precipitates of Cr(III), Fe(III) hydroxides and Cr(x)Fe(1-)(x)(OH)(3) and thus reduce surface passivation of Fe(0). Edetic Acid 77-81 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 18563354-7 2008 The reduced adhesion by EPS was correlated with suppressed expression of MCP-1 and IL-8, the major chemokines in IBD. eps 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 18487223-4 2008 Blockade of CXC chemokine receptor-2 signaling using a small molecule antagonist (AZ10397767) attenuated the IL-8-induced increases in AR expression and transcriptional activity. AZ10397767 82-92 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 18487223-7 2008 In addition, our data show that IL-8-promoted regulation of the AR attenuates the effectiveness of the AR antagonist bicalutamide in reducing CaP cell viability. bicalutamide 117-129 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 18486963-5 2008 This enhancement is attributed to the formation of complex compounds between EDTA/NaF and reaction products, such as Cr(III) and Fe(III), which eliminate the precipitates of Cr(III), Fe(III) hydroxides and Cr(x)Fe(1-)(x)(OH)(3) and thus reduce surface passivation of Fe(0). tris(1,10-phenanthroline)chromium(III) chloride 117-124 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 18486963-5 2008 This enhancement is attributed to the formation of complex compounds between EDTA/NaF and reaction products, such as Cr(III) and Fe(III), which eliminate the precipitates of Cr(III), Fe(III) hydroxides and Cr(x)Fe(1-)(x)(OH)(3) and thus reduce surface passivation of Fe(0). ferric sulfate 129-136 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 18486963-5 2008 This enhancement is attributed to the formation of complex compounds between EDTA/NaF and reaction products, such as Cr(III) and Fe(III), which eliminate the precipitates of Cr(III), Fe(III) hydroxides and Cr(x)Fe(1-)(x)(OH)(3) and thus reduce surface passivation of Fe(0). tris(1,10-phenanthroline)chromium(III) chloride 174-181 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 18486963-5 2008 This enhancement is attributed to the formation of complex compounds between EDTA/NaF and reaction products, such as Cr(III) and Fe(III), which eliminate the precipitates of Cr(III), Fe(III) hydroxides and Cr(x)Fe(1-)(x)(OH)(3) and thus reduce surface passivation of Fe(0). fe(iii) hydroxides 183-201 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 18486963-5 2008 This enhancement is attributed to the formation of complex compounds between EDTA/NaF and reaction products, such as Cr(III) and Fe(III), which eliminate the precipitates of Cr(III), Fe(III) hydroxides and Cr(x)Fe(1-)(x)(OH)(3) and thus reduce surface passivation of Fe(0). Chromium 117-119 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 18486963-5 2008 This enhancement is attributed to the formation of complex compounds between EDTA/NaF and reaction products, such as Cr(III) and Fe(III), which eliminate the precipitates of Cr(III), Fe(III) hydroxides and Cr(x)Fe(1-)(x)(OH)(3) and thus reduce surface passivation of Fe(0). Iron 129-131 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 18622147-0 2008 [Association between raised IL-8 serum levels and resistance to combined peg-interferon plus ribavirin therapy in HCV+ active chronic hepatitis]. Ribavirin 93-102 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 18514500-6 2008 High chlorobenzene concentrations (100 g/m(3)) induced IL-8 production in A549 cells, whereby lower concentrations (10 microg/m(3)-1 g/m(3)) stimulated the secretion of the monocyte chemoattractant protein-1 (MCP-1). chlorobenzene 5-18 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 18000644-11 2008 CONCLUSIONS: mRNA expression levels of IL-8 and GSK-3beta correlate with antitumor activity of enzastaurin. enzastaurin 95-106 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 18622147-7 2008 Serum IL-8 can be considered and proposed as a non-invasive and predictive marker of response to combined PEG IFN alpha2b + Ribavirin in CAH HCV +. Polyethylene Glycols 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 18622147-7 2008 Serum IL-8 can be considered and proposed as a non-invasive and predictive marker of response to combined PEG IFN alpha2b + Ribavirin in CAH HCV +. Ribavirin 124-133 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 18363812-8 2008 IL10 and SU6656 had no effect on PMA formation, although both significantly reduced TF (P = 0.002 and P = 0.02) and IL8 (P = 0.009 and P = 0.001) mRNA upon TRAP and P-selectin stimulation. SU 6656 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 18598184-8 2008 Resveratrol at concentrations > or =50 micromol/mL significantly inhibited IL-8 and IL-6 production. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 18598184-10 2008 Quercetin 3"-sulfate, at 25 micromol/mL, inhibited IL-8 and IL-6 production. quercetin 3'-sulfate 0-20 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 18473409-12 2008 CONCLUSION: In group A (oral NAC combined with mesalamine) contrarily to group B (mesalamine alone), the clinical improvement correlates with a decrease of chemokines such as MCP-1 and IL-8. Mesalamine 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 18535989-9 2008 Quantitative reverse-transcriptase polymerase chain reaction (qRTPCR) of IL-8 mRNA shows increased expression in the high-dose RNT-treated groups at both 1 and 6 h, while an adhesion molecule, ICAM-1 mRNA, shows the greatest increase at 6 h in the QM-treated group. glutaminylmethionine 248-250 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 18433103-5 2008 Stevioside (2 mM) potentiated TNF-alpha-mediated IL-8 release in T84 cells. stevioside 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 18433103-6 2008 However, steviol (0.01-0.2 mM) significantly suppressed TNF-alpha-induced IL-8 release in all three cell lines. steviol 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 18433103-9 2008 Two biological effects of steviol in the colon are demonstrated for the first time: stimulation of Cl(-) secretion and attenuation of TNF-alpha-stimulated IL-8 production. steviol 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 18294142-1 2008 We have demonstrated that LPA (lysophosphatidic acid)-induced IL (interleukin)-8 secretion was partly mediated via transactivation of EGFR [EGF (epidermal growth factor) receptor] in HBEpCs (human bronchial epithelial primary cells). lysophosphatidic acid 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 62-80 18294142-1 2008 We have demonstrated that LPA (lysophosphatidic acid)-induced IL (interleukin)-8 secretion was partly mediated via transactivation of EGFR [EGF (epidermal growth factor) receptor] in HBEpCs (human bronchial epithelial primary cells). lysophosphatidic acid 31-52 C-X-C motif chemokine ligand 8 Homo sapiens 62-80 18569862-4 2008 In the present study, we show that human peripheral blood mononuclear cells (PBMC) co-cultured with PG, in the presence of the inflammatory activator lipopolysaccharide, secreted higher amounts of pro-inflammatory and pro-angiogenic cytokines, such as interleukin (IL)-1beta, IL-6 and IL-8. pg 100-102 C-X-C motif chemokine ligand 8 Homo sapiens 285-289 18245149-7 2008 In contrast, infectious rhinovirus impaired lipopolysaccharide and lipoteichoic acid induced TNFalpha and IL8 secretion by macrophages. lipoteichoic acid 67-84 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 18444659-0 2008 5-caffeoylquinic acid and caffeic acid down-regulate the oxidative stress- and TNF-alpha-induced secretion of interleukin-8 from Caco-2 cells. 5'-O-caffeoylquinic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 18444659-0 2008 5-caffeoylquinic acid and caffeic acid down-regulate the oxidative stress- and TNF-alpha-induced secretion of interleukin-8 from Caco-2 cells. caffeic acid 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 18444659-2 2008 We investigated in this study the down-regulative effects of 5-caffeoylquinic acid (CQA), the predominant isomer of CHA, on the H(2)O(2-) or TNF-alpha-induced secretion of interleukin (IL)-8, a central pro-inflammatory chemokine involved in the pathogenesis of inflammatory bowel diseases, in human intestinal epithelial Caco-2 cells. 5'-O-caffeoylquinic acid 61-82 C-X-C motif chemokine ligand 8 Homo sapiens 172-190 18444659-2 2008 We investigated in this study the down-regulative effects of 5-caffeoylquinic acid (CQA), the predominant isomer of CHA, on the H(2)O(2-) or TNF-alpha-induced secretion of interleukin (IL)-8, a central pro-inflammatory chemokine involved in the pathogenesis of inflammatory bowel diseases, in human intestinal epithelial Caco-2 cells. Amodiaquine 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 172-190 18444659-3 2008 After the cells had been pre- and simultaneously treated with CQA, the oversecretion of IL-8 and overexpression of its mRNA induced by H(2)O(2) were significantly suppressed in a dose-dependent manner in the range of 0.25-2.00 mmol/L. Amodiaquine 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 18444659-3 2008 After the cells had been pre- and simultaneously treated with CQA, the oversecretion of IL-8 and overexpression of its mRNA induced by H(2)O(2) were significantly suppressed in a dose-dependent manner in the range of 0.25-2.00 mmol/L. Hydrogen Peroxide 135-143 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 18444659-4 2008 We further found that a metabolite of CQA, caffeic acid (CA), but not quinic acid, significantly inhibited the H(2)O(2)-induced IL-8 secretion and its mRNA expression in the same dose-dependent manner. Amodiaquine 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 18444659-4 2008 We further found that a metabolite of CQA, caffeic acid (CA), but not quinic acid, significantly inhibited the H(2)O(2)-induced IL-8 secretion and its mRNA expression in the same dose-dependent manner. caffeic acid 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 18444659-4 2008 We further found that a metabolite of CQA, caffeic acid (CA), but not quinic acid, significantly inhibited the H(2)O(2)-induced IL-8 secretion and its mRNA expression in the same dose-dependent manner. Hydrogen Peroxide 111-119 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 18444659-6 2008 Caffeic acid at 2.00 mmol/l was able to absolutely block the H(2)O(2)- or TNF-alpha-induced oversecretion of IL-8 in Caco-2 cells. caffeic acid 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 18444659-6 2008 Caffeic acid at 2.00 mmol/l was able to absolutely block the H(2)O(2)- or TNF-alpha-induced oversecretion of IL-8 in Caco-2 cells. Hydrogen Peroxide 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 18464996-4 2008 Precipitation of adenine was increased by salts (NaCl and NaF) whereas it was prevented by DMSO, in agreement with the involvement of hydrophobic interactions (pi-pi stacking) in the vertical stacking of adenine molecules. Adenine 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 18292390-9 2008 Finally, human macrophages acquire responsiveness to the CXCR2 ligands (IL-8 and Grobeta), as measured by superoxide anion production, after induction of CXCR2 expression by PPAR-gamma ligands. Superoxides 106-122 C-X-C motif chemokine ligand 8 Homo sapiens 72-88 18079491-6 2008 beta-tryptase also up-regulated IL-8 mRNA expression, as analyzed by RT-PCR and real-time PCR, which was abolished by the transcription inhibitor actinomycin D. Dactinomycin 146-159 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 18096868-4 2008 NiSO(4) (200 muM) synergistically enhanced CXCL8, yet antagonized CXCL10 mRNA expression and protein release from HLF in response to MALP-2. niso 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 18096868-7 2008 The COX-2 inhibitor, NS-398, attenuated NiSO(4) and MALP-2-induced PGE2 and CXCL8 release and partially reversed the NiSO(4)-dependent inhibition of MALP-2-induced CXCL10 release from HLF. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 76-81 18096868-7 2008 The COX-2 inhibitor, NS-398, attenuated NiSO(4) and MALP-2-induced PGE2 and CXCL8 release and partially reversed the NiSO(4)-dependent inhibition of MALP-2-induced CXCL10 release from HLF. niso 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 76-81 18397832-2 2008 We found for the first time that the secretion of interleukin-8 (IL-8) in intestinal epithelial cells stimulated by hydrogen peroxide or TNF-alpha was suppressed in the presence of carnosine (beta-Ala-His), a dietary dipeptide. Hydrogen Peroxide 116-133 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 18325031-0 2008 Montelukast inhibits tumour necrosis factor-alpha-mediated interleukin-8 expression through inhibition of nuclear factor-kappaB p65-associated histone acetyltransferase activity. montelukast 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 18325031-3 2008 METHODS: We examined the inhibitory effects of montelukast on TNF-alpha-induced IL-8 production in PMA-differentiated U-937 cells. montelukast 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 18325031-10 2008 Montelukast induced a concentration-dependent inhibition of TNF-alpha-induced IL-8 release and mRNA expression that reached a plateau at 0.1 microm without affecting cell viability. montelukast 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 18325031-12 2008 CONCLUSION: Montelukast inhibits TNF-alpha-stimulated IL-8 expression through changes in NF-kappaB p65-associated HAT activity. montelukast 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 18358739-12 2008 The effects of acute CS exposure appear to encompass both up-regulation of chemotaxis mechanisms through IL-8, but also down-regulation of innate immunity. Cesium 21-23 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 18397832-4 2008 The inhibitory effect of carnosine on the IL-8 secretion differed from that of other histidine-containing dipeptides like Gly-His, Ala-His, and anserine (beta-Ala-1-methyl-His), which inhibited both the hydrogen peroxide-induced secretion and mRNA expression of IL-8. beta-ala-1-methyl-his 154-175 C-X-C motif chemokine ligand 8 Homo sapiens 262-266 18397832-2 2008 We found for the first time that the secretion of interleukin-8 (IL-8) in intestinal epithelial cells stimulated by hydrogen peroxide or TNF-alpha was suppressed in the presence of carnosine (beta-Ala-His), a dietary dipeptide. Hydrogen Peroxide 116-133 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 18397832-2 2008 We found for the first time that the secretion of interleukin-8 (IL-8) in intestinal epithelial cells stimulated by hydrogen peroxide or TNF-alpha was suppressed in the presence of carnosine (beta-Ala-His), a dietary dipeptide. 2-(3-azaniumylpropanoylamino)-3-(1H-imidazol-5-yl)propanoate 192-204 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 18397832-2 2008 We found for the first time that the secretion of interleukin-8 (IL-8) in intestinal epithelial cells stimulated by hydrogen peroxide or TNF-alpha was suppressed in the presence of carnosine (beta-Ala-His), a dietary dipeptide. 2-(3-azaniumylpropanoylamino)-3-(1H-imidazol-5-yl)propanoate 192-204 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 18397832-2 2008 We found for the first time that the secretion of interleukin-8 (IL-8) in intestinal epithelial cells stimulated by hydrogen peroxide or TNF-alpha was suppressed in the presence of carnosine (beta-Ala-His), a dietary dipeptide. Dipeptides 217-226 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 18397832-2 2008 We found for the first time that the secretion of interleukin-8 (IL-8) in intestinal epithelial cells stimulated by hydrogen peroxide or TNF-alpha was suppressed in the presence of carnosine (beta-Ala-His), a dietary dipeptide. Dipeptides 217-226 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 19288836-1 2008 This study sought to evaluate the microhardness of enamel submitted to 10% carbamide peroxide treatment and different methods of remineralization involving sodium fluoride (NaF). Sodium Fluoride 156-171 C-X-C motif chemokine ligand 8 Homo sapiens 173-176 17669408-9 2008 Treatment of FTEC with TLR3 agonist poly(I:C) resulted in increased expression of interleukin-8, tumor-necrosis factor alpha, human beta-defensin 2, interferon beta, and interferon stimulated genes myxovirus resistance gene 1, 2",5"-oligoadenylate synthetase, and protein kinase R. Additionally, FTEC exposed to poly(I:C) also resulted in the induction of TLR2, TLR3, and TLR7. poly 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 82-124 17669408-9 2008 Treatment of FTEC with TLR3 agonist poly(I:C) resulted in increased expression of interleukin-8, tumor-necrosis factor alpha, human beta-defensin 2, interferon beta, and interferon stimulated genes myxovirus resistance gene 1, 2",5"-oligoadenylate synthetase, and protein kinase R. Additionally, FTEC exposed to poly(I:C) also resulted in the induction of TLR2, TLR3, and TLR7. Carbon 16-17 C-X-C motif chemokine ligand 8 Homo sapiens 82-124 19288836-5 2008 Based on these results, NaF therapies are recommended during carbamide peroxide bleaching treatments. Carbamide Peroxide 61-79 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 18715885-3 2008 The time courses for silica-induced release of tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, and IL-8 both from co-cultures and monocyte mono-cultures showed an early peak at 5-10 h, almost no response at 20 h, and a strong increase at 43 h. At 43 h, co-cultures also showed strongly increased IL-6 levels. Silicon Dioxide 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 18715885-4 2008 Steady-state levels of mRNA roughly exhibited the same pattern of early up-regulation and reduced levels at 20 h. Compared with monocyte mono-cultures, silica induced a strong release of IL-1beta, IL-6, and IL-8, but not of TNF-alpha, after 43 h in co-cultures, whereas at 5 and 10 h a significant difference was only observed for the silica-induced IL-8 response. Silicon Dioxide 152-158 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 18715885-4 2008 Steady-state levels of mRNA roughly exhibited the same pattern of early up-regulation and reduced levels at 20 h. Compared with monocyte mono-cultures, silica induced a strong release of IL-1beta, IL-6, and IL-8, but not of TNF-alpha, after 43 h in co-cultures, whereas at 5 and 10 h a significant difference was only observed for the silica-induced IL-8 response. Silicon Dioxide 152-158 C-X-C motif chemokine ligand 8 Homo sapiens 350-354 18080321-3 2008 Our experiments showed that protein production and mRNA expressions of MMP-1, MMP-3, MMP-13, IL-8, MCP-1, and RANTES were downregulated by treatment with glucosamine in HPSFs. Glucosamine 154-165 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 18464055-9 2008 Sources of fine PM and their relative contributions varied across the sampling sites and a strong linear association was observed between IL-8 and secondary sulfate from coal combustion (r(2) = .79). Sulfates 157-164 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 18464055-10 2008 Ultrafine vanadium, lead, copper, and sulfate were also associated with increases in IL-8. ultrafine vanadium 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 18464055-10 2008 Ultrafine vanadium, lead, copper, and sulfate were also associated with increases in IL-8. Copper 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 18464055-10 2008 Ultrafine vanadium, lead, copper, and sulfate were also associated with increases in IL-8. Sulfates 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17729256-8 2008 The amounts of interleukin-6 and interleukin-8 proinflammatory cytokines released from human blood leukocytes exposed to the polyurethane scaffolds in vitro were comparable and/or lower than the amount of the cytokines released by leukocytes exposed to the culture-grade polystyrene control. Polyurethanes 125-137 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 17966119-9 2008 P was the most effective inhibitor of IL-8 release; IL-8 was significantly decreased after exposure to un, tri, tetra and penta but significantly increased after JP-8 exposure compared with controls. Phosphorus 0-1 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 18080321-6 2008 The results suggest that the inhibition of MMP-1, -3, and -13 expressions as well as IL-8, MCP-1, and RANTES productions by GLN might mediate suppression of NF-kappaB signal pathways, and HPSFs seem to have a potential functions as an alternative source of MMPs and chemokines for inducing the degradation of cartilage in OA. Glucosamine 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 18544909-8 2008 Inhibition of extracellular signal-regulated kinase (ERK), one of the MAPK pathways, suppressed the IL-8 production induced by both 2,4-dinitrochlorobenzene (DNCB) and nickel sulfate (NiSO(4)), and inhibition of p38 MAPK, a second MAPK pathway, significantly suppressed IL-8 production induced by only DNCB. Dinitrochlorobenzene 132-156 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 18544909-8 2008 Inhibition of extracellular signal-regulated kinase (ERK), one of the MAPK pathways, suppressed the IL-8 production induced by both 2,4-dinitrochlorobenzene (DNCB) and nickel sulfate (NiSO(4)), and inhibition of p38 MAPK, a second MAPK pathway, significantly suppressed IL-8 production induced by only DNCB. Dinitrochlorobenzene 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 18007587-5 2008 Moreover, downregulation of Hsp27 increased the release of the pro-inflammatory cytokine IL-8 from TNF-alpha-stimulated and UV-irradiated keratinocytes, and this increase was inhibited by pretreatment with the NF-kappaB inhibitor BAY11-7082. 3-(4-methylphenylsulfonyl)-2-propenenitrile 230-240 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 18034171-4 2008 9(S)-HODE evoked intracellular calcium mobilization and secretion of cytokines, including IL-6, IL-8, and GM-CSF in NHEK cells. 9(S)-HODE 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 18353383-7 2008 Urine interleukin-8 was negatively associated with urothelial heparin-binding epidermal growth factor-like growth factor staining (r = -0.34; 95% CI -0.55, -0.12; p = 0.002) and positively associated with lamina propria mast cell count (r = 0.29; 95% CI 0.06, 0.52; p = 0.01). Heparin 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 6-19 18544909-8 2008 Inhibition of extracellular signal-regulated kinase (ERK), one of the MAPK pathways, suppressed the IL-8 production induced by both 2,4-dinitrochlorobenzene (DNCB) and nickel sulfate (NiSO(4)), and inhibition of p38 MAPK, a second MAPK pathway, significantly suppressed IL-8 production induced by only DNCB. Dinitrochlorobenzene 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 270-274 18442745-0 2008 Involvement of mitogen-activated protein kinases and nuclear factor-kappa B activation in nitric oxide-induced interleukin-8 expression in human pulp cells. Nitric Oxide 90-102 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 18544909-8 2008 Inhibition of extracellular signal-regulated kinase (ERK), one of the MAPK pathways, suppressed the IL-8 production induced by both 2,4-dinitrochlorobenzene (DNCB) and nickel sulfate (NiSO(4)), and inhibition of p38 MAPK, a second MAPK pathway, significantly suppressed IL-8 production induced by only DNCB. nickel sulfate 168-182 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 18544909-8 2008 Inhibition of extracellular signal-regulated kinase (ERK), one of the MAPK pathways, suppressed the IL-8 production induced by both 2,4-dinitrochlorobenzene (DNCB) and nickel sulfate (NiSO(4)), and inhibition of p38 MAPK, a second MAPK pathway, significantly suppressed IL-8 production induced by only DNCB. niso 184-188 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 18544909-8 2008 Inhibition of extracellular signal-regulated kinase (ERK), one of the MAPK pathways, suppressed the IL-8 production induced by both 2,4-dinitrochlorobenzene (DNCB) and nickel sulfate (NiSO(4)), and inhibition of p38 MAPK, a second MAPK pathway, significantly suppressed IL-8 production induced by only DNCB. niso 184-188 C-X-C motif chemokine ligand 8 Homo sapiens 270-274 18544909-8 2008 Inhibition of extracellular signal-regulated kinase (ERK), one of the MAPK pathways, suppressed the IL-8 production induced by both 2,4-dinitrochlorobenzene (DNCB) and nickel sulfate (NiSO(4)), and inhibition of p38 MAPK, a second MAPK pathway, significantly suppressed IL-8 production induced by only DNCB. Dinitrochlorobenzene 302-306 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 18544909-9 2008 Additionally, neutralization of TNF-alpha activity suppressed IL-8 production in THP-1 cells exposed to DNCB and NiSO(4). Dinitrochlorobenzene 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 18544909-9 2008 Additionally, neutralization of TNF-alpha activity suppressed IL-8 production in THP-1 cells exposed to DNCB and NiSO(4). niso 113-117 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 18544909-10 2008 In conclusion, IL-8 production was predominantly induced in THP-1 cells following allergen stimulation, and MAPK pathways and TNF-alpha were involved in the IL-8 production induced by DNCB and NiSO(4). Dinitrochlorobenzene 184-188 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 18544909-10 2008 In conclusion, IL-8 production was predominantly induced in THP-1 cells following allergen stimulation, and MAPK pathways and TNF-alpha were involved in the IL-8 production induced by DNCB and NiSO(4). niso 193-197 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 18442745-4 2008 RESULTS: Sodium nitroprusside (SNP), an NO donor, has increased IL-8 secretion and mRNA expression in a dose- and time-dependent manner. Nitroprusside 9-29 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 18442745-1 2008 OBJECTIVE: This study examined the effect of nitric oxide (NO) on interleukin-8 (IL-8) production and the involvement of mitogen-activated protein kinase (MAPK) and nuclear factor-kappa B (NF-kappaB) signaling pathways in primary cultured human pulp cells. Nitric Oxide 45-57 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 18390748-5 2008 Furthermore, inhibition of Pyk2 activity in these cells by transduction with the catalytically inactive Pyk2 mutant, transfection with Pyk2-specific small interfering RNA, or treatment with Tyrphostin A9 significantly blocked LPS-induced IL-8 production. tyrphostin A9 190-203 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 18953964-0 2008 [The mechanism of inhibition by ginkgolide B on interleukin-8 production induced by 4-hydroxynonenal in bronchial epithelial cells]. ginkgolide B 32-44 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 18953964-0 2008 [The mechanism of inhibition by ginkgolide B on interleukin-8 production induced by 4-hydroxynonenal in bronchial epithelial cells]. 4-hydroxy-2-nonenal 84-100 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 18953964-1 2008 OBJECTIVE: 4-Hydroxynonenal (4-HNE) can increase the synthesis of interleukin-8 (IL-8) in bronchial epithelium cells (16HBE). 4-hydroxy-2-nonenal 11-27 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 18953964-1 2008 OBJECTIVE: 4-Hydroxynonenal (4-HNE) can increase the synthesis of interleukin-8 (IL-8) in bronchial epithelium cells (16HBE). 4-hydroxy-2-nonenal 11-27 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 18953964-1 2008 OBJECTIVE: 4-Hydroxynonenal (4-HNE) can increase the synthesis of interleukin-8 (IL-8) in bronchial epithelium cells (16HBE). 4-hydroxy-2-nonenal 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 18953964-1 2008 OBJECTIVE: 4-Hydroxynonenal (4-HNE) can increase the synthesis of interleukin-8 (IL-8) in bronchial epithelium cells (16HBE). 4-hydroxy-2-nonenal 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 18953964-2 2008 This study was to explore the role of ginkgolide B in inhibiting the synthesis of IL-8 induced by 4-HNE in 16HBE. ginkgolide B 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 18953964-2 2008 This study was to explore the role of ginkgolide B in inhibiting the synthesis of IL-8 induced by 4-HNE in 16HBE. 4-hydroxy-2-nonenal 98-103 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 18953964-2 2008 This study was to explore the role of ginkgolide B in inhibiting the synthesis of IL-8 induced by 4-HNE in 16HBE. 16hbe 107-112 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 18953964-8 2008 RESULTS: The level of IL-8 in 10 micromol/L 4-HNE, 100 micromol/L ginkgolide B + 10 micromol/L 4-HNE, the control groups after 4-HNE stimulating for 4 h were (98.3 +/- 4.2), (88.2 +/- 5.3), (65.3 +/- 6. 4-hydroxy-2-nonenal 44-49 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 18953964-12 2008 The expression of IL-8 and the AP-1 combining activity in groups of pre-incubated with PD98059 2 hours before 4-HNE stimulation were lower than that without PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 87-94 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 18953964-12 2008 The expression of IL-8 and the AP-1 combining activity in groups of pre-incubated with PD98059 2 hours before 4-HNE stimulation were lower than that without PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 157-164 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 18953964-15 2008 Ginkgolide B inhibited synthesis of IL-8 by blocking ERK1-AP1 transduction pathways. ginkgolide B 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 18646527-0 2008 [Effect of Zn2+ on level of IL-8 and TNF-alpha mRNA and protein expressed of human II alveolar epithelial cells]. Zinc 11-15 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 18646527-1 2008 OBJECTIVE: To study the effect of Zn2+ on levels of the cytokines IL-8 and TNF-alpha mRNA expression of human II alveolar epithelial cell. Zinc 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 18646527-3 2008 RESULTS: Incubation of A549 cells with Zn2+ for 3 h and 24h could stimulate the accumulations of IL-8 and TNF-alpha mRNA and protein of A549 cells in a concentration-dependent manner. Zinc 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 18646527-4 2008 CONCLUSION: The production of IL-8 and TNF-alpha mRNA and protein from A549 cells stimulated by Zn2+ could be important source of cytokines in respiratory damage induced by Zn2+. Zinc 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 18646527-4 2008 CONCLUSION: The production of IL-8 and TNF-alpha mRNA and protein from A549 cells stimulated by Zn2+ could be important source of cytokines in respiratory damage induced by Zn2+. Zinc 173-177 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 18252714-0 2008 Toll-like receptor 4 mediates induction of the Bcl10-NFkappaB-interleukin-8 inflammatory pathway by carrageenan in human intestinal epithelial cells. Carrageenan 100-111 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 18252714-1 2008 The sulfated polysaccharide carrageenan (CGN) induces activation of NFkappaB and interleukin 8 (IL-8) in human colonic epithelial cells through a pathway of innate immunity mediated by Bcl10 (B-cell CLL/lymphoma 10). Polysaccharides 13-27 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 18252714-1 2008 The sulfated polysaccharide carrageenan (CGN) induces activation of NFkappaB and interleukin 8 (IL-8) in human colonic epithelial cells through a pathway of innate immunity mediated by Bcl10 (B-cell CLL/lymphoma 10). Polysaccharides 13-27 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 18252714-1 2008 The sulfated polysaccharide carrageenan (CGN) induces activation of NFkappaB and interleukin 8 (IL-8) in human colonic epithelial cells through a pathway of innate immunity mediated by Bcl10 (B-cell CLL/lymphoma 10). Carrageenan 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 18252714-1 2008 The sulfated polysaccharide carrageenan (CGN) induces activation of NFkappaB and interleukin 8 (IL-8) in human colonic epithelial cells through a pathway of innate immunity mediated by Bcl10 (B-cell CLL/lymphoma 10). Carrageenan 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 18252714-1 2008 The sulfated polysaccharide carrageenan (CGN) induces activation of NFkappaB and interleukin 8 (IL-8) in human colonic epithelial cells through a pathway of innate immunity mediated by Bcl10 (B-cell CLL/lymphoma 10). Carrageenan 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 18252714-1 2008 The sulfated polysaccharide carrageenan (CGN) induces activation of NFkappaB and interleukin 8 (IL-8) in human colonic epithelial cells through a pathway of innate immunity mediated by Bcl10 (B-cell CLL/lymphoma 10). Carrageenan 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 18276593-8 2008 The EGFR inhibitor AG1478, completely blocked IL-8 and ICAM-1 expression to basal levels, as did the specific Erk1/2 inhibitor U0126. RTKI cpd 19-25 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 18400717-8 2008 IL-8 production was significantly decreased by troglitazone, ALA, DHA, EPA, and GLA. Troglitazone 47-59 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18276593-9 2008 The p38 mitogen-activated protein kinase inhibitor SB203580 blocked IL-8 secretion but not ICAM-1 expression, whereas the PI3K inhibitor wortmannin was ineffective in both responses. SB 203580 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 18400717-8 2008 IL-8 production was significantly decreased by troglitazone, ALA, DHA, EPA, and GLA. alpha-Linolenic Acid 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18400717-12 2008 Addition of GW9662 reversed the effect of troglitazone and PUFAs at 0.1 mumol/L on IL-8 production and decreased the expression of PPARgamma. 2-chloro-5-nitrobenzanilide 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 18400717-8 2008 IL-8 production was significantly decreased by troglitazone, ALA, DHA, EPA, and GLA. Docosahexaenoic Acids 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18400717-12 2008 Addition of GW9662 reversed the effect of troglitazone and PUFAs at 0.1 mumol/L on IL-8 production and decreased the expression of PPARgamma. Troglitazone 42-54 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 18400717-8 2008 IL-8 production was significantly decreased by troglitazone, ALA, DHA, EPA, and GLA. Eicosapentaenoic Acid 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18400717-12 2008 Addition of GW9662 reversed the effect of troglitazone and PUFAs at 0.1 mumol/L on IL-8 production and decreased the expression of PPARgamma. Fatty Acids, Unsaturated 59-64 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 18400717-8 2008 IL-8 production was significantly decreased by troglitazone, ALA, DHA, EPA, and GLA. gamma-Linolenic Acid 80-83 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18299991-3 2008 In cultured human aortic endothelial cells (HAEC), arterial shear stress of 10 dyne/cm(2) blocked by >80% the induction by 5 ng/mL TNFalpha of interleukin-8 (IL-8) and IL-6 secretion (50 and 90% reduction, respectively, in the presence of nitric oxide synthase antagonism with 200 microM nitro-L-arginine methylester, L-NAME). Nitroarginine 291-307 C-X-C motif chemokine ligand 8 Homo sapiens 146-159 18299991-3 2008 In cultured human aortic endothelial cells (HAEC), arterial shear stress of 10 dyne/cm(2) blocked by >80% the induction by 5 ng/mL TNFalpha of interleukin-8 (IL-8) and IL-6 secretion (50 and 90% reduction, respectively, in the presence of nitric oxide synthase antagonism with 200 microM nitro-L-arginine methylester, L-NAME). NG-Nitroarginine Methyl Ester 321-327 C-X-C motif chemokine ligand 8 Homo sapiens 146-159 18234309-6 2008 RESULTS: Human embryonic kidney 293 transfectants mimicking this heterozygous mutation produced less IL-8 when stimulated with lipoteichoic acid (LTA), heat-inactivated Staphylococcus aureus or triacylated lipopeptides requiring the TLR-2/1 heterodimer. lipoteichoic acid 127-144 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 18207234-3 2008 Removal of inflammatory cytokines TNF, IL-6, IL-1beta and IL-8 was assessed by filtering cytokine spiked human plasma through the walls of the carbon modules under pressure. Carbon 143-149 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 18307536-7 2008 IL-8 expression was inducible by hypoxia mimicking reagent cobalt chloride. cobaltous chloride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18094008-7 2008 EGF-CM contained significant neutrophil chemotactic activity involving granulocyte-macrophage colony-stimulating factor and interleukin-8 that was potentiated by leukotriene B(4). Leukotriene B4 162-175 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 18234317-9 2008 Malondialdehyde levels were inversely associated with forced vital capacity and FEV(1) and positively associated with IL-8 levels in nasal lavage. Malondialdehyde 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 18199004-3 2008 LTC 4 affects the GSH/GSSG ratio by activating signals to increase interleukin-8 (IL-8) production. Glutathione 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 18199004-3 2008 LTC 4 affects the GSH/GSSG ratio by activating signals to increase interleukin-8 (IL-8) production. Glutathione 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 18199004-3 2008 LTC 4 affects the GSH/GSSG ratio by activating signals to increase interleukin-8 (IL-8) production. Glutathione Disulfide 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 18199004-3 2008 LTC 4 affects the GSH/GSSG ratio by activating signals to increase interleukin-8 (IL-8) production. Glutathione Disulfide 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 18199004-4 2008 Pretreatment with a reducing agent, glutathione monochrome ester (GSH-OEt), and with a leukotriene receptor antagonist, montelukast, significantly suppressed LTC(4)-induced time-dependent changes in the intracellular redox state, and also suppressed upregulation of IL-8 production by suppressing NF-kappaB activation. glutathione monochrome ester 36-64 C-X-C motif chemokine ligand 8 Homo sapiens 266-270 18199004-4 2008 Pretreatment with a reducing agent, glutathione monochrome ester (GSH-OEt), and with a leukotriene receptor antagonist, montelukast, significantly suppressed LTC(4)-induced time-dependent changes in the intracellular redox state, and also suppressed upregulation of IL-8 production by suppressing NF-kappaB activation. S-ethyl glutathione 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 266-270 18199004-4 2008 Pretreatment with a reducing agent, glutathione monochrome ester (GSH-OEt), and with a leukotriene receptor antagonist, montelukast, significantly suppressed LTC(4)-induced time-dependent changes in the intracellular redox state, and also suppressed upregulation of IL-8 production by suppressing NF-kappaB activation. montelukast 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 266-270 18212111-1 2008 The production of interleukin-8 induced by the activation of protease-activated receptor 2 and its synergism with interleukin-1beta were modulated by 14-membered-ring macrolides, namely, roxithromycin, erythromycin, and clarithromycin, in cultured normal human epidermal keratinocytes. Roxithromycin 187-200 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 18212111-1 2008 The production of interleukin-8 induced by the activation of protease-activated receptor 2 and its synergism with interleukin-1beta were modulated by 14-membered-ring macrolides, namely, roxithromycin, erythromycin, and clarithromycin, in cultured normal human epidermal keratinocytes. Erythromycin 202-214 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 18212111-1 2008 The production of interleukin-8 induced by the activation of protease-activated receptor 2 and its synergism with interleukin-1beta were modulated by 14-membered-ring macrolides, namely, roxithromycin, erythromycin, and clarithromycin, in cultured normal human epidermal keratinocytes. Clarithromycin 220-234 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 18212111-2 2008 Those macrolides may attenuate the protease-activated receptor 2-interleukin-8 axis and thereby modulate proinflammatory responses in the skin. Macrolides 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 18005471-8 2008 The interleukins were significantly higher at some perioperative time points in the fentanyl group compared to the remifentanil group (tumour necrosis factor: T5: 3.57 vs. 2.37; IL-6: T5: 4.62 vs. 3.73; and IL-8: T5: 4.43 vs. 2.65 and T6: 2.61 vs. 1.13). Fentanyl 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 18395088-11 2008 IL-8 expression was dependent on COX-2-mediated prostaglandin E(2) synthesis. Dinoprostone 48-66 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18395088-12 2008 In the presence of an NF-kappaB inhibitor MG132, IL-8 transcription was inhibited, but not that of COX-2. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 42-47 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 18377624-1 2008 We developed a method for the quantitative determination of sodium fluoride (NaF), sodium monofluorophosphate (SMFP) and amine fluoride (AmF) in toothpastes on the Belgian market. Sodium Fluoride 60-75 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 18234309-6 2008 RESULTS: Human embryonic kidney 293 transfectants mimicking this heterozygous mutation produced less IL-8 when stimulated with lipoteichoic acid (LTA), heat-inactivated Staphylococcus aureus or triacylated lipopeptides requiring the TLR-2/1 heterodimer. lipoteichoic acid 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 18415826-0 2008 Effect of budesonide and formoterol on IL-6 and IL-8 release from primary bronchial epithelial cells. Formoterol Fumarate 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 18415826-5 2008 Budesonide attenuated the IL-6 and IL-8 release, an inhibiting effect that was sustained, but not reinforced, by formoterol. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 18234309-6 2008 RESULTS: Human embryonic kidney 293 transfectants mimicking this heterozygous mutation produced less IL-8 when stimulated with lipoteichoic acid (LTA), heat-inactivated Staphylococcus aureus or triacylated lipopeptides requiring the TLR-2/1 heterodimer. Lipopeptides 206-218 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 18297698-2 2008 This study was undertaken to determine whether SK, either alone or in combination with quercitin (QT) is able to modulate the release of IL-6 and IL-8 from peripheral blood mononuclear cells (PBMCs). Quercetin 87-96 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 18354227-0 2008 Molecular characterization of Helicobacter pylori VacA induction of IL-8 in U937 cells reveals a prominent role for p38MAPK in activating transcription factor-2, cAMP response element binding protein, and NF-kappaB activation. Cyclic AMP 162-166 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 18354227-4 2008 Furthermore, an intracellular Ca(2+) chelator (BAPTA-AM), which inhibited VacA-activated p38 MAPK, caused a dose-dependent reduction in VacA-induced IL-8 secretion by U937 cells, implying a role for intracellular Ca(2+) in mediating activation of MAPK and the canonical NF-kappaB pathway. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 18297698-2 2008 This study was undertaken to determine whether SK, either alone or in combination with quercitin (QT) is able to modulate the release of IL-6 and IL-8 from peripheral blood mononuclear cells (PBMCs). Quercetin 98-100 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 18297698-5 2008 On the contrary, incubation with SK and QT at both concentrations (10 and 100 nM) produced a significant increase in the release of IL-8 as compared to other groups (4.19 +/- 0.82, SK-QT 10 nM; 3.83 +/- 1.17 SK-QT 100 nM, P < 0.05 vs. baseline 1.00 +/- 0.10, Tamiflu 100 nM 1.35 +/- 0.16, SK 10 nM 1.68 +/- 0.15 and SK 100 nM 1.80 +/- 0.48). Oseltamivir 262-269 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 18349372-3 2008 In contrast, arginine-specific gingipain 2 (RgpB) increased IL-8 production. Arginine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 18234802-0 2008 Epstein-Barr virus lytic transactivator Zta enhances chemotactic activity through induction of interleukin-8 in nasopharyngeal carcinoma cells. zta 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 18234802-6 2008 Further studies showed that the EBV lytic transactivator Zta is a potent inducer of IL-8 in NPC cells, augmenting secreted and intracellular IL-8 proteins, as well as IL-8 RNA. zta 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 18234802-6 2008 Further studies showed that the EBV lytic transactivator Zta is a potent inducer of IL-8 in NPC cells, augmenting secreted and intracellular IL-8 proteins, as well as IL-8 RNA. zta 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 18234802-6 2008 Further studies showed that the EBV lytic transactivator Zta is a potent inducer of IL-8 in NPC cells, augmenting secreted and intracellular IL-8 proteins, as well as IL-8 RNA. zta 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 18234802-7 2008 Zta upregulates Egr-1, a cellular transcription factor that has been involved in upregulation of IL-8, but the Zta-induced IL-8 expression is independent of Egr-1. zta 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 18234802-7 2008 Zta upregulates Egr-1, a cellular transcription factor that has been involved in upregulation of IL-8, but the Zta-induced IL-8 expression is independent of Egr-1. zta 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 18234802-8 2008 The ability of Zta to transactivate the IL-8 promoter is important for the induction of IL-8, and we have identified two Zta-responsive elements in the promoter. zta 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 18234802-8 2008 The ability of Zta to transactivate the IL-8 promoter is important for the induction of IL-8, and we have identified two Zta-responsive elements in the promoter. zta 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 18234802-8 2008 The ability of Zta to transactivate the IL-8 promoter is important for the induction of IL-8, and we have identified two Zta-responsive elements in the promoter. zta 121-124 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 18234802-9 2008 Zta can bind to these two elements in vitro and can also be recruited to the IL-8 promoter in vivo. zta 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 18234802-10 2008 DNA-binding-defective Zta mutants can neither activate the IL-8 promoter nor induce IL-8 production. zta 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 18234802-10 2008 DNA-binding-defective Zta mutants can neither activate the IL-8 promoter nor induce IL-8 production. zta 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 18234802-11 2008 In addition, Zta-expressing NPC cells exert enhanced chemotactic activity that is mainly mediated by IL-8. zta 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 18380907-9 2008 CONCLUSION: Gram-positive or gram-negative bacteria activate human ASMC to release CXCL-8. asmc 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 83-89 18206243-0 2008 IL-8 production and AP-1 transactivation induced by UVA in human keratinocytes: roles of D-alpha-tocopherol. alpha-Tocopherol 89-107 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18206243-2 2008 Here, we investigated the role of D-alpha-tocopherol in the regulation of IL-8 production and AP-1 binding activity in UVA-irradiated human keratinocytes. alpha-Tocopherol 34-52 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 18206243-7 2008 These results demonstrated that D-alpha-tocopherol may be able to prevent the IL-8 upregulation and the increase in AP-1 activation induced by UVA irradiation through down-modulating cellular oxidative stress. alpha-Tocopherol 32-50 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 17986175-9 2008 Viable and motile spermatozoa attached to PMN without being phagocytosed within 60 min (45 +/- 3%), whereas binding to sodium fluoride (NaF)-immobilized spermatozoa was reduced to 20 +/- 2%. Sodium Fluoride 119-134 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 18380907-12 2008 Our findings that ASMC can respond directly to gram-negative and gram-positive bacteria by releasing the neutrophil selective chemokine, CXCL-8, is consistent with what we know about the role of neutrophil recruitment in bacterial infections in the lung. asmc 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 137-143 19124359-9 2008 CONCLUSION: In ex-smokers with severe COPD, a measure of local pulmonary inflammation, FENO, may be more closely associated with FEV1 responses to four weeks of ICS than are standard markers of systemic inflammation, serum CRP, IL-6, and IL-8. flubendiamide 87-91 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 17724435-10 2008 SB203580 also prevented the CytoMix-induced permeability increase and reduced NO, IL-6, and IL-8 levels. SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 18343055-5 2008 Dose-dependent increases in NF-kappaB activity and IL-8 secretion were observed, reaching 1.4- and 7.6-fold, respectively using DON at 10 microg/ml. deoxynivalenol 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 18343055-9 2008 These data show that DON induces NF-kappaB activation and IL-8 secretion dose-dependently in Caco-2 cells, and this effect was accentuated upon pro-inflammatory stimulation, suggesting DON exposure could cause or exacerbate intestinal inflammation. deoxynivalenol 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 18343055-9 2008 These data show that DON induces NF-kappaB activation and IL-8 secretion dose-dependently in Caco-2 cells, and this effect was accentuated upon pro-inflammatory stimulation, suggesting DON exposure could cause or exacerbate intestinal inflammation. deoxynivalenol 185-188 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 18308354-5 2008 Deoxynivalenol was the only mycotoxin able to directly increase IL-8 secretion (10- to 15-fold increase). deoxynivalenol 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 18308354-7 2008 We found that deoxynivalenol, ochratoxin A and patulin all potentiated the effect of IL-1beta on IL-8 secretion (ranging from 35% to 138% increase) and increased the transepithelial passage of commensal bacteria (ranging from 12- to 1544-fold increase). deoxynivalenol 14-28 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 18308354-7 2008 We found that deoxynivalenol, ochratoxin A and patulin all potentiated the effect of IL-1beta on IL-8 secretion (ranging from 35% to 138% increase) and increased the transepithelial passage of commensal bacteria (ranging from 12- to 1544-fold increase). ochratoxin A 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 18242599-0 2008 Acetylcholine mediates the release of IL-8 in human bronchial epithelial cells by a NFkB/ERK-dependent mechanism. Acetylcholine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 18664200-3 2008 The modulation of cetirizine on the production of interferon (IFN)-gamma, interleukin (IL)-1beta, IL-6 and IL-8 in HaCaT cells and fibroblasts was measured by ELISA. Cetirizine 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 18664200-6 2008 Cetirizine 1-100 micromol x L(-1) inhibited SP-induced IL-1beta and IL-8 production in HaCaT cells and fibroblasts, while had no effect on the production of IFN-gamma in both cells. cetirizine 1 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 18664200-8 2008 These findings suggest that cetirizine may be involved in the treatment of SP-induced skin inflammation by inhibiting the expression of substance P receptor and regulation the production of IL-1beta and IL-8 in epidermal keratinocyte and dermal fibroblasts. Cetirizine 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 18191106-12 2008 Analysis of the proangiogenic factors IL-8 and VEGF showed significant reduction in IL-8 production by moxifloxacin and ciprofloxacin up to 48% and in VEGF secretion from the cells. Moxifloxacin 103-115 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 18191106-12 2008 Analysis of the proangiogenic factors IL-8 and VEGF showed significant reduction in IL-8 production by moxifloxacin and ciprofloxacin up to 48% and in VEGF secretion from the cells. Moxifloxacin 103-115 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 18191106-12 2008 Analysis of the proangiogenic factors IL-8 and VEGF showed significant reduction in IL-8 production by moxifloxacin and ciprofloxacin up to 48% and in VEGF secretion from the cells. Ciprofloxacin 120-133 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 18242599-4 2008 Additionally, we tested the IL-8-mediated neutrophil chemotactic activity of 16HBE supernatants stimulated with acetylcholine in the presence or absence of tiotropium. 16hbe 77-82 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 18242599-4 2008 Additionally, we tested the IL-8-mediated neutrophil chemotactic activity of 16HBE supernatants stimulated with acetylcholine in the presence or absence of tiotropium. Acetylcholine 112-125 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 18242599-6 2008 Acetylcholine (10 microM) significantly stimulated ERK1/2 and NFkB activation as well as IL-8 release in 16HBE cells when compared to basal values. Acetylcholine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 18242599-8 2008 Additionally, acetylcholine-mediated IL-8 release from 16HBE cells significantly increased chemotaxis toward neutrophils and this effect was blocked by tiotropium. Acetylcholine 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 18242599-8 2008 Additionally, acetylcholine-mediated IL-8 release from 16HBE cells significantly increased chemotaxis toward neutrophils and this effect was blocked by tiotropium. Tiotropium Bromide 152-162 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 18242599-9 2008 In conclusion, acetylcholine activates the release of IL-8 from 16HBE involving PKC, ERK1/2 and NFkB pathways via muscarinic receptors, suggesting that it is likely to contribute to IL-8 related neutrophilic inflammatory disorders in the airway. Acetylcholine 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 18242599-9 2008 In conclusion, acetylcholine activates the release of IL-8 from 16HBE involving PKC, ERK1/2 and NFkB pathways via muscarinic receptors, suggesting that it is likely to contribute to IL-8 related neutrophilic inflammatory disorders in the airway. Acetylcholine 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 18289803-8 2008 Overall, these data highlight an AhR-dependent regulation of IL-8 in response to BP that likely contributes to the airway inflammatory effects of this environmental chemical. Benzo(a)pyrene 81-83 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 18281166-5 2008 Meanwhile, treatment with actinomycin D facilitated the Trp-P-1-induced down-regulation of IL-8 expression in LPS-stimulated THP-1 cells, implying that the inhibition might be due to a decrease in the stability of IL-8 mRNA rather than an attenuation of IL-8 transcription. Dactinomycin 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 18281166-0 2008 3-Amino-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1) attenuates LPS-induced IL-8 expression by decreasing mRNA stability in THP-1 cells. 3-amino-1,4-dimethyl-5H-pyrido(4,3-b)indole 0-43 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 17915188-1 2008 Using human osteoblastic SaM-1 cells, we investigated the effects of lysophosphatidic acid (LPA) on the production of interleukin (IL)-6 and IL-8, molecules which are capable of stimulating the development of osteoclasts from their haematopoietic precursors, and examined the signal transduction systems involved in their effect on these cells. lysophosphatidic acid 69-90 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 18281166-5 2008 Meanwhile, treatment with actinomycin D facilitated the Trp-P-1-induced down-regulation of IL-8 expression in LPS-stimulated THP-1 cells, implying that the inhibition might be due to a decrease in the stability of IL-8 mRNA rather than an attenuation of IL-8 transcription. Dactinomycin 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 18281166-5 2008 Meanwhile, treatment with actinomycin D facilitated the Trp-P-1-induced down-regulation of IL-8 expression in LPS-stimulated THP-1 cells, implying that the inhibition might be due to a decrease in the stability of IL-8 mRNA rather than an attenuation of IL-8 transcription. Dactinomycin 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 18281166-7 2008 Exogenous addition of ionomycin rescued both the IL-8 protein levels and phosphorylation of p38 MAP kinase inhibited by Trp-P-1. Ionomycin 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 18289803-0 2008 Interleukin-8 induction by the environmental contaminant benzo(a)pyrene is aryl hydrocarbon receptor-dependent and leads to lung inflammation. Benzo(a)pyrene 57-71 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 18289803-3 2008 In primary human macrophages, BP was shown to induce IL-8 expression at both mRNA and secretion levels in a dose-dependent manner. Benzo(a)pyrene 30-32 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 18289803-4 2008 Such an up-regulation was likely linked to aryl hydrocarbon receptor (AhR)-activation since BP-mediated IL-8 induction was reduced after AhR expression knock-down through RNA interference. Benzo(a)pyrene 92-94 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 18289803-5 2008 Moreover, electrophoretic mobility shift assays (EMSAs) and chromatin immunoprecipitation experiments showed BP-triggered binding of AhR to a consensus xenobiotic responsive element (XRE) found in the human IL-8 promoter. Benzo(a)pyrene 109-111 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 18352197-1 2008 Axially localized NaF dopants are coated onto Al cylindrical wire arrays in order to act as spectroscopic tracers in the stagnated z-pinch plasma. Aluminum 46-48 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 17915188-1 2008 Using human osteoblastic SaM-1 cells, we investigated the effects of lysophosphatidic acid (LPA) on the production of interleukin (IL)-6 and IL-8, molecules which are capable of stimulating the development of osteoclasts from their haematopoietic precursors, and examined the signal transduction systems involved in their effect on these cells. lysophosphatidic acid 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 17915188-4 2008 The expression of IL-6 and IL-8 mRNAs was maximal at 1-3h, and the increase in IL-6 and IL-8 synthesis in response to lysophosphatidic acid (1-10 microM) occurred in a concentration-dependent manner. lysophosphatidic acid 118-139 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 17915188-4 2008 The expression of IL-6 and IL-8 mRNAs was maximal at 1-3h, and the increase in IL-6 and IL-8 synthesis in response to lysophosphatidic acid (1-10 microM) occurred in a concentration-dependent manner. lysophosphatidic acid 118-139 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 17915188-7 2008 The pretreatment of SaM-1 cells with U-73122, a phospholipase C (PLC) inhibitor, and 2-APB also inhibited the increase in IL-6 and IL-8 synthesis in response to LPA. 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 17915188-7 2008 The pretreatment of SaM-1 cells with U-73122, a phospholipase C (PLC) inhibitor, and 2-APB also inhibited the increase in IL-6 and IL-8 synthesis in response to LPA. lysophosphatidic acid 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 17915188-8 2008 These findings suggest that extracellular LPA-induced IL-6 and IL-8 synthesis occurred through Edg-2 (LPA(1) receptor) and the activation of PLC and IP(3)-mediated intracellular calcium release in SaM-1 cells. lysophosphatidic acid 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 18266269-4 2008 PPG 1200 was the most potent inhibitor tested, shown for TNF, IL-1beta, IL-6, IL-8, IL-10 and TGF-beta induction, and displayed no cytotoxic effects. ppg 1200 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 18356657-5 2008 Compared with the conventional group, the mini-CPB group had lower levels of IL-8 on postoperative day 1 (8.3 +/- 6.4 vs. 19 +/- 11 pg/mL, p = 0.016) and of neutrophil elastase on postoperative days 1 (127 +/- 52 vs. 240 +/- 100 microg/L, p = 0.013) and 2 (107 +/- 17 vs. 170 +/- 45 micro/L, p = 0.0001). cpb 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 18226915-5 2008 All chemokines except RANTES were significantly high in PF compared to BL in TB group, whereas IL-8 and MCP-1 showed significant increase only in NTB PF. ntb pf 146-152 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 17786963-5 2008 The HNP-induced IL-8 production was blocked by the Src tyrosine kinase inhibitor PP2, MEK1/2 inhibitor U0126, and the phosphatidylinositol 3 kinase (PI3K) inhibitor LY294002, but not by the JNK inhibitor SP600125 in both cell types. pyrazolanthrone 204-212 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 17786963-6 2008 Treatment with the p38 inhibitor SB203580 attenuated the HNP-induced IL-8 production only in monocytes. SB 203580 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 17786963-5 2008 The HNP-induced IL-8 production was blocked by the Src tyrosine kinase inhibitor PP2, MEK1/2 inhibitor U0126, and the phosphatidylinositol 3 kinase (PI3K) inhibitor LY294002, but not by the JNK inhibitor SP600125 in both cell types. U 0126 103-108 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 18354287-9 2008 Only initial IL-8 was associated with increased Pao2/Fio2 (P = .013) and with a minimum Pao2/Fio2 >200 (P = .042) during 72 hours. pao2 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 17786963-5 2008 The HNP-induced IL-8 production was blocked by the Src tyrosine kinase inhibitor PP2, MEK1/2 inhibitor U0126, and the phosphatidylinositol 3 kinase (PI3K) inhibitor LY294002, but not by the JNK inhibitor SP600125 in both cell types. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 165-173 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 18171700-0 2008 Lysophosphatidic acid up-regulates expression of interleukin-8 and -6 in granulosa-lutein cells through its receptors and nuclear factor-kappaB dependent pathways: implications for angiogenesis of corpus luteum and ovarian hyperstimulation syndrome. lysophosphatidic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 49-69 18171700-14 2008 LPA induced IL-8 and IL-6 through different pathways. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 18171700-15 2008 LPA-induced IL-8 and IL-6 increased permeability of human umbilical vein endothelial cell monolayer. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 18171700-16 2008 CONCLUSIONS: LPA induces IL-8 and IL-6 expressions through LPA receptors and nuclear factor-kappaB dependent pathways in granulosa-lutein cells. lysophosphatidic acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 18171700-18 2008 Large amounts of LPA-induced IL-8 and IL-6 from multiple corpora luteae of stimulated ovaries may be one of the pathophysiological causes of ovarian hyperstimulation syndrome. lysophosphatidic acid 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 18354287-9 2008 Only initial IL-8 was associated with increased Pao2/Fio2 (P = .013) and with a minimum Pao2/Fio2 >200 (P = .042) during 72 hours. fio2 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 18354287-9 2008 Only initial IL-8 was associated with increased Pao2/Fio2 (P = .013) and with a minimum Pao2/Fio2 >200 (P = .042) during 72 hours. pao2 88-92 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 18354287-9 2008 Only initial IL-8 was associated with increased Pao2/Fio2 (P = .013) and with a minimum Pao2/Fio2 >200 (P = .042) during 72 hours. fio2 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 18344608-2 2008 GL, as well as dexamethasone (DEX) inhibited both tumor necrosis factor (TNF)-alpha- and IL-1beta-induced IL-8 production, mRNA expression, and promoter activity in A549 cells. Dexamethasone 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 18292514-6 2008 Engagement of 2DL4 was also shown to activate the transcription and translation of a variety of cytokine genes, including TNF-alpha, IFN-gamma, MIP1alpha, MIP1beta, and IL-8. 2dl4 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 18292514-7 2008 Pharmacological inhibitors of JNK, MEK1/2 and p38, blocked IFN-gamma, IL-8, and MIP1alpha production, suggesting that MAPKs are regulating 2DL4-mediated cytokine production in a nonredundant manner. 2dl4 139-143 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 18344608-0 2008 Glycyrrhizin inhibits interleukin-8 production and nuclear factor-kappaB activity in lung epithelial cells, but not through glucocorticoid receptors. Glycyrrhizic Acid 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 18344608-2 2008 GL, as well as dexamethasone (DEX) inhibited both tumor necrosis factor (TNF)-alpha- and IL-1beta-induced IL-8 production, mRNA expression, and promoter activity in A549 cells. Glycyrrhizic Acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 18344608-2 2008 GL, as well as dexamethasone (DEX) inhibited both tumor necrosis factor (TNF)-alpha- and IL-1beta-induced IL-8 production, mRNA expression, and promoter activity in A549 cells. Dexamethasone 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 18071189-5 2008 Ox-PAPE-N-biotin, like Ox-PAPC, induced interleukin-8 (IL-8) protein synthesis and stimulated IL-8, low density lipoprotein receptor, heme oxygenase-1, and activating transcription factor-3 mRNA expression in HAECs. ox-pape 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 18071189-5 2008 Ox-PAPE-N-biotin, like Ox-PAPC, induced interleukin-8 (IL-8) protein synthesis and stimulated IL-8, low density lipoprotein receptor, heme oxygenase-1, and activating transcription factor-3 mRNA expression in HAECs. ox-pape 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 18071189-5 2008 Ox-PAPE-N-biotin, like Ox-PAPC, induced interleukin-8 (IL-8) protein synthesis and stimulated IL-8, low density lipoprotein receptor, heme oxygenase-1, and activating transcription factor-3 mRNA expression in HAECs. ox-pape 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 18071189-5 2008 Ox-PAPE-N-biotin, like Ox-PAPC, induced interleukin-8 (IL-8) protein synthesis and stimulated IL-8, low density lipoprotein receptor, heme oxygenase-1, and activating transcription factor-3 mRNA expression in HAECs. n-biotin 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 18071189-5 2008 Ox-PAPE-N-biotin, like Ox-PAPC, induced interleukin-8 (IL-8) protein synthesis and stimulated IL-8, low density lipoprotein receptor, heme oxygenase-1, and activating transcription factor-3 mRNA expression in HAECs. n-biotin 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 18071189-5 2008 Ox-PAPE-N-biotin, like Ox-PAPC, induced interleukin-8 (IL-8) protein synthesis and stimulated IL-8, low density lipoprotein receptor, heme oxygenase-1, and activating transcription factor-3 mRNA expression in HAECs. n-biotin 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 18344608-5 2008 Furthermore, only GL inhibited DNA binding of p65 to the IL-8 promoter region. Glycyrrhizic Acid 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 18344608-6 2008 These findings indicated that GL had a glucocorticoid-like inhibitory effect on IL-8 production via a mechanism that differs from that of glucocorticoids. Glycyrrhizic Acid 30-32 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 17997161-6 2008 Interestingly, PGN-induced IL-8 expression was inhibited by nystatin, a specific inhibitor for lipid rafts, but not by chlorpromazine, a specific inhibitor for clathrin-coated pits. Nystatin 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 18093085-10 2008 IL-8 levels were higher in infants with hypoxemia and inversely related with SaO(2) levels. sao(2) 77-83 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18066713-3 2008 When coincubating A549 with LPS and meta-iodobenzylguanidine or novobiocin, selective arginine-dependent ART-inhibitors, the release of IL-6 and IL-8 was inhibited in a concentration-dependent manner. 3-Iodobenzylguanidine 36-60 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 18066713-3 2008 When coincubating A549 with LPS and meta-iodobenzylguanidine or novobiocin, selective arginine-dependent ART-inhibitors, the release of IL-6 and IL-8 was inhibited in a concentration-dependent manner. Novobiocin 64-74 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 18066713-3 2008 When coincubating A549 with LPS and meta-iodobenzylguanidine or novobiocin, selective arginine-dependent ART-inhibitors, the release of IL-6 and IL-8 was inhibited in a concentration-dependent manner. Arginine 86-94 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 18089838-7 2008 TCDD-mediated inductions of various AhR targets, such as the drug metabolizing CYP1B1, the cytokine interleukin-1beta, the chemokines interleukin-8 and CCL1, the adhesion molecule beta7 integrin, and the AhR repressor, were also prevented by KN-93 in human macrophages. Polychlorinated Dibenzodioxins 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 134-147 18079996-6 2008 The magnitude of the postoperative increase in plasma MIF was associated with increased number of days required for mechanical ventilation (r = 0.553; P = 0.012), and peak plasma IL-8 correlated significantly with the fraction of inhaled oxygen (FiO(2)) required immediately after surgery (r = 0.510; P = 0.02). Oxygen 238-244 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 18477937-10 2008 IL-6 secretion was elevated in all hyperoxic groups at 24 hrs (p < .001), and both IL-6 and IL-8 levels were greater in the 40% FiO2 group compared with all other groups at 72 hrs (p < .01). fio2 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 18214943-8 2008 Zn supplementation was marginally effective in reducing percentage increase in plasma IL-6 and IL-8 while increasing the percentage change in ex vivo generation of IL-2 in isolated mononuclear cell. Zinc 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 18327406-8 2008 Under serum-free conditions, heparin demonstrated dose-dependent anti-inflammatory effects, significantly reducing secretion of pro-inflammatory cytokines (IL-1beta, IL-6, IL-8, and TNF-alpha) in response to LPS-stimulation of THP-1 cells and primary monocytes. Heparin 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 18630691-0 2008 [Effect of N-acetylcysteine on lipopolysaccharide stimulating IL-8 expression of human uterine smooth cell]. Acetylcysteine 11-27 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 18630691-1 2008 OBJECTIVE: To investigate the effects of N-acetylcysteine (NAC)on the expression of IL-8 and the activity of NF-kappaB, which are induced by lipopolysaccharide (LPS) in human uterine smooth cell. Acetylcysteine 41-57 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 18191873-12 2008 Interestingly, ET-1-induced production of IL-8 was also inhibited by celecoxib. Celecoxib 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 18494145-9 2008 The lack of IL-8 production by trimellitic anhydride can be explained by the rapid hydrolysis of this chemical in water to trimellitic acid, which is not an allergen. trimellitic anhydride 31-52 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 17996917-0 2008 Fluoride-induced IL-8 release in human epithelial lung cells: relationship to EGF-receptor-, SRC- and MAP-kinase activation. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 18494145-9 2008 The lack of IL-8 production by trimellitic anhydride can be explained by the rapid hydrolysis of this chemical in water to trimellitic acid, which is not an allergen. trimellitic acid 123-139 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 18494145-13 2008 By Western blot analysis we could indeed demonstrate p38 activation by all chemical allergens tested and, using the selective p38 MAPK inhibitor SB203580, a significant modulation of allergen-induced IL-8 release could be achieved in all cases. SB 203580 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 17583554-5 2008 hMSCs, induced to differentiate with osteogenic medium (OGM) containing ascorbate, beta-glycerophosphate (beta-GP), and dexamethasone (DEX), showed an increase in mRNA and protein secretion of the ELR(+) CXC chemokines CXCL8 and CXCL1. beta-glycerophosphoric acid 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 219-224 17583554-5 2008 hMSCs, induced to differentiate with osteogenic medium (OGM) containing ascorbate, beta-glycerophosphate (beta-GP), and dexamethasone (DEX), showed an increase in mRNA and protein secretion of the ELR(+) CXC chemokines CXCL8 and CXCL1. Dexamethasone 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 219-224 17583554-8 2008 Inhibition of the glucocorticoid receptor with mifepristone only partially inhibits DEX-stimulated CXCL8 expression indicating both glucocorticoid receptor dependent and independent pathways. Mifepristone 47-59 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 17583554-8 2008 Inhibition of the glucocorticoid receptor with mifepristone only partially inhibits DEX-stimulated CXCL8 expression indicating both glucocorticoid receptor dependent and independent pathways. Dexamethasone 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 17996917-4 2008 The ERK1/2-inhibitor PD98059, the p38-inhibitor SB202190 and the JNK1/2-inhibitor SP600125 partially inhibited the fluoride-induced IL-8 response. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 17996917-4 2008 The ERK1/2-inhibitor PD98059, the p38-inhibitor SB202190 and the JNK1/2-inhibitor SP600125 partially inhibited the fluoride-induced IL-8 response. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 17996917-4 2008 The ERK1/2-inhibitor PD98059, the p38-inhibitor SB202190 and the JNK1/2-inhibitor SP600125 partially inhibited the fluoride-induced IL-8 response. pyrazolanthrone 82-90 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 17996917-4 2008 The ERK1/2-inhibitor PD98059, the p38-inhibitor SB202190 and the JNK1/2-inhibitor SP600125 partially inhibited the fluoride-induced IL-8 response. Fluorides 115-123 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 17996917-6 2008 Treatment with siRNA against JNK2 also reduced the IL-8 response to fluoride. Fluorides 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 17996917-10 2008 AG1478, an EGFR-inhibitor, partially reduced the fluoride-induced IL-8 response and the phosphorylation of JNK1/2 and ERK1/2, but less the phosphorylation of p38. RTKI cpd 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17996917-10 2008 AG1478, an EGFR-inhibitor, partially reduced the fluoride-induced IL-8 response and the phosphorylation of JNK1/2 and ERK1/2, but less the phosphorylation of p38. Fluorides 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 18642783-10 2008 The levels of TNF-alpha, IL-6, and IL-8 of the high concentration Gln 2 h groups were all significantly higher then those of the concentration Gln 0.5 h groups (all P <0.01), however, there was not significant difference in the level of IL-1beta between the high concentration 0.5 h and 2 h Gln groups. Glutamine 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 17981896-7 2008 On the other hand, in the presence of ATP (3 mM) and beryllium fluoride (10 mM NaF and 300 microM BeCl(2)), we observed the formation of a stable symmetric complex, suggesting the existence of a transiently formed symmetric complex during the chaperonin cycle. Adenosine Triphosphate 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 17981896-7 2008 On the other hand, in the presence of ATP (3 mM) and beryllium fluoride (10 mM NaF and 300 microM BeCl(2)), we observed the formation of a stable symmetric complex, suggesting the existence of a transiently formed symmetric complex during the chaperonin cycle. beryllium fluoride 53-71 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 18250478-9 2008 We have confirmed the increased expression of P2Y(6) by challenging intestinal epithelial cell-6 and Caco-2/15 cells with TNF-alpha and IFN-gamma and showing that stimulation of epithelial cells by UDP results in an increased expression and release of CXCL8 by an ERK1/2-dependent mechanism. Uridine Diphosphate 198-201 C-X-C motif chemokine ligand 8 Homo sapiens 252-257 17996917-12 2008 In conclusion, our findings suggest that the fluoride-induced IL-8 release involves the combined activation of ERK1/2, JNK1/2 and p38, and that the phosphorylation of these kinases, and in particular JNK1/2 and ERK1/2, partly, is mediated via a SFK-dependent EGFR-linked pathway. Fluorides 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 17996917-1 2008 Exposure of human epithelial lung cells to fluorides is known to induce a marked increase in the release of interleukin (IL)-8, a chemokine involved in neutrophil recruitment. Fluorides 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 108-126 18155175-1 2008 BACKGROUND: In a previous report (Higai K et al., Biol Pharm Bull, 2007), glycated human serum albumin (Glc-HSA) was found to induce interleukin-8 (IL-8) mRNA expression in human monocyte-derived U937 cells through a reactive oxygen species (ROS)-dependent pathway; however, Glc-HSA signaling has not been elucidated in macrophages. Reactive Oxygen Species 217-240 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 17709599-4 2008 Using CF bronchial epithelial cells (IB3-1) in vitro, exogenous PGE-2 induces IL-8 release in a dose-dependent manner. Dinoprostone 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 17709599-6 2008 Inhibition of cyclooxygenase (Cox)-2 with NS-398 was associated with reductions in Cox-2 (2-fold) and IL-6 (1.3-fold) mRNA transcripts, and in IL-8 and PGE-2 chemokine secretion. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 17709599-9 2008 We conclude that PGE-2 stimulates IL-8 production through the CHOP transcription factor in CF cells. Dinoprostone 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 17970647-3 2008 Surprisingly, treatment of MonoMac6 cells with the natural PPARgamma ligand 15-deoxy-Delta12,14-prostaglandin J2 led to increased cytokine (IL-8) release in response to either TNF-alpha or CS extract (CSE). 14-prostaglandin j2 93-112 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 17970647-3 2008 Surprisingly, treatment of MonoMac6 cells with the natural PPARgamma ligand 15-deoxy-Delta12,14-prostaglandin J2 led to increased cytokine (IL-8) release in response to either TNF-alpha or CS extract (CSE). Cesium 189-191 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 18155175-1 2008 BACKGROUND: In a previous report (Higai K et al., Biol Pharm Bull, 2007), glycated human serum albumin (Glc-HSA) was found to induce interleukin-8 (IL-8) mRNA expression in human monocyte-derived U937 cells through a reactive oxygen species (ROS)-dependent pathway; however, Glc-HSA signaling has not been elucidated in macrophages. Reactive Oxygen Species 217-240 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 18155175-1 2008 BACKGROUND: In a previous report (Higai K et al., Biol Pharm Bull, 2007), glycated human serum albumin (Glc-HSA) was found to induce interleukin-8 (IL-8) mRNA expression in human monocyte-derived U937 cells through a reactive oxygen species (ROS)-dependent pathway; however, Glc-HSA signaling has not been elucidated in macrophages. Reactive Oxygen Species 242-245 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 18155175-1 2008 BACKGROUND: In a previous report (Higai K et al., Biol Pharm Bull, 2007), glycated human serum albumin (Glc-HSA) was found to induce interleukin-8 (IL-8) mRNA expression in human monocyte-derived U937 cells through a reactive oxygen species (ROS)-dependent pathway; however, Glc-HSA signaling has not been elucidated in macrophages. Reactive Oxygen Species 242-245 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 18155175-1 2008 BACKGROUND: In a previous report (Higai K et al., Biol Pharm Bull, 2007), glycated human serum albumin (Glc-HSA) was found to induce interleukin-8 (IL-8) mRNA expression in human monocyte-derived U937 cells through a reactive oxygen species (ROS)-dependent pathway; however, Glc-HSA signaling has not been elucidated in macrophages. Glucose 104-107 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 18155175-1 2008 BACKGROUND: In a previous report (Higai K et al., Biol Pharm Bull, 2007), glycated human serum albumin (Glc-HSA) was found to induce interleukin-8 (IL-8) mRNA expression in human monocyte-derived U937 cells through a reactive oxygen species (ROS)-dependent pathway; however, Glc-HSA signaling has not been elucidated in macrophages. Glucose 104-107 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 17975552-6 2008 Consistent with repression of canonical IKK signaling pathway, the induction of NF-kappaB target genes monocyte chemoattractant protein, intercellular adhesion molecule-1, cyclooxygenase-2 and IL-8 is also inhibited by R-Roscovitine. Roscovitine 219-232 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 18037374-0 2008 Simvastatin enhances endothelial differentiation of peripheral blood mononuclear cells in hypercholesterolemic patients and induces pro-angiogenic cytokine IL-8 secretion from monocytes. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 18181043-12 2008 Concentrations of IL-8 and VEGF in the conditioned medium of OUR-10 and NC65 cells also decreased following DEX treatment, with the inhibition of nuclear translocation of NF-kappa B. Dexamethasone 108-111 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 18181043-13 2008 CONCLUSION: DEX treatment is a candidate for advanced RCC therapy by inhibiting the activation of NF-kappa B and its downstream products such as IL-6, IL-8 and VEGF. Dexamethasone 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 18037374-11 2008 In response to simvastatin, IL-8 was mainly increased in monocyte culture supernatants while VEGF increased in smooth muscle cell culture supernatants. Simvastatin 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 18037374-14 2008 CONCLUSION: Simvastatin enhances endothelial differentiation of peripheral blood mononuclear cells in patients with hypercholesterolemia and increases pro-angiogenic cytokine IL-8 secretion from monocytes. Simvastatin 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 17555752-1 2008 OBJECTIVE: To evaluate the influence of peroxisome proliferator-activated receptor-gamma (PPAR gamma) ligand (pioglitazone) on tumor necrosis factor-alpha (TNF-alpha)-induced interleukin-8 (IL-8) expression in endometriotic stromal cells (ESCs) and on proliferation of ESCs. Pioglitazone 110-122 C-X-C motif chemokine ligand 8 Homo sapiens 175-188 18259970-4 2008 This study examined the effects of fluticasone, salmeterol, and agents which raise intracellular cAMP (cilomilast and db-cAMP) on the expression of IP-10 and IL-8 protein and mRNA. Fluticasone 35-46 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 18259970-4 2008 This study examined the effects of fluticasone, salmeterol, and agents which raise intracellular cAMP (cilomilast and db-cAMP) on the expression of IP-10 and IL-8 protein and mRNA. Salmeterol Xinafoate 48-58 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 18259970-4 2008 This study examined the effects of fluticasone, salmeterol, and agents which raise intracellular cAMP (cilomilast and db-cAMP) on the expression of IP-10 and IL-8 protein and mRNA. Cyclic AMP 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 18259970-4 2008 This study examined the effects of fluticasone, salmeterol, and agents which raise intracellular cAMP (cilomilast and db-cAMP) on the expression of IP-10 and IL-8 protein and mRNA. Cilomilast 103-113 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 18259970-4 2008 This study examined the effects of fluticasone, salmeterol, and agents which raise intracellular cAMP (cilomilast and db-cAMP) on the expression of IP-10 and IL-8 protein and mRNA. Bucladesine 118-125 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 18259970-7 2008 Fluticasone (0.1 nM to 1 microM) increased IP-10 but reduced IL-8 protein release without changing IP-10 mRNA levels assessed by real time RT-PCR. Fluticasone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 18222974-9 2008 In addition, MEVA attenuated the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated secretion of tumor necrosis factor-alpha, interleukin-6 (IL-6), and IL-8 in human mast cells. ANAVACYM protocol 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 18222974-9 2008 In addition, MEVA attenuated the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated secretion of tumor necrosis factor-alpha, interleukin-6 (IL-6), and IL-8 in human mast cells. Tetradecanoylphorbol Acetate 33-64 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 18222974-9 2008 In addition, MEVA attenuated the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated secretion of tumor necrosis factor-alpha, interleukin-6 (IL-6), and IL-8 in human mast cells. Calcium 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 18222974-9 2008 In addition, MEVA attenuated the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated secretion of tumor necrosis factor-alpha, interleukin-6 (IL-6), and IL-8 in human mast cells. Calcimycin 87-93 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 18222974-9 2008 In addition, MEVA attenuated the phorbol 12-myristate 13-acetate and calcium ionophore A23187 (PMACI)-stimulated secretion of tumor necrosis factor-alpha, interleukin-6 (IL-6), and IL-8 in human mast cells. pmaci 95-100 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 17555752-7 2008 We determined the effect of pioglitazone on the production of TNF-alpha-induced IL-8 protein in culture supernatant of ESCs using ELISA. Pioglitazone 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 17555752-13 2008 Treating ESCs with 0.1-10 microM of pioglitazone significantly reduced the TNF-alpha-induced IL-8 production. Pioglitazone 36-48 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 17555752-18 2008 CONCLUSION(S): The present study demonstrates for the first time that PPAR gamma is expressed in ESCs, and that pioglitazone reduced IL-8 secretion and the proliferation of ESCs. Pioglitazone 112-124 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 18195160-10 2008 Circulating concentrations of osteopontin, monocyte chemoattractant protein-1, basic fibroblast growth factor, interleukin-8, and interleukin-10 were significantly reduced only by eplerenone. Eplerenone 180-190 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 17941093-0 2008 Characterization of epithelial IL-8 response to inflammatory bowel disease mucosal E. coli and its inhibition by mesalamine. Mesalamine 113-123 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 17662042-9 2008 IFN-gamma inhibited phorbol 12-myristate 13-acetate (PMA)-induced release of IL-8 and CCL1 (by 47 and 38%). Tetradecanoylphorbol Acetate 20-51 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 17662042-9 2008 IFN-gamma inhibited phorbol 12-myristate 13-acetate (PMA)-induced release of IL-8 and CCL1 (by 47 and 38%). Tetradecanoylphorbol Acetate 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 17662042-12 2008 IFN-gamma-induced inhibition of chemokine expression and release was NO dependent, as treatment with the NOS inhibitor N(G)-nitro-l-arginine methyl ester (l-NAME) reduced the IFN-gamma inhibitory effect on IL-8 and CCL1 mRNA expression. NG-Nitroarginine Methyl Ester 155-161 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 17941093-9 2008 IL-8 release was mediated by extracellular-regulated kinase (ERK) and p38 mitogen-activated protein kinase (MAPK) and inhibited by mesalamine, but not hydrocortisone, at therapeutic concentrations. Mesalamine 131-141 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 17662042-12 2008 IFN-gamma-induced inhibition of chemokine expression and release was NO dependent, as treatment with the NOS inhibitor N(G)-nitro-l-arginine methyl ester (l-NAME) reduced the IFN-gamma inhibitory effect on IL-8 and CCL1 mRNA expression. NG-Nitroarginine Methyl Ester 119-153 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 17913284-3 2008 Column tests comparing pure NaF solutions, synthetic SPL solutions, and actual SPL leachate indicate that the complex chemical matrix of the SPL leachate can impact fluoride removal significantly. Fluorides 165-173 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 18203325-2 2008 We have also reported that a certain pharmacological concentration of simvastatin, i.e., 0.05-0.1 microM, inhibits the production of interleukin 6 (IL-6) and IL-8 and the cell proliferation induced by tumor necrosis factor-alpha (TNF-alpha) in fibroblast-like synoviocytes (FLS) derived from patients with RA in vitro. Simvastatin 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 18203325-11 2008 CONCLUSION: These data, together with our previous report, suggest that low (pharmacological range) and high concentrations of simvastatin affect FLS differently: (1) at a low concentration, it inhibits IL-6 and IL-8 production and the cell proliferation of FLS induced by TNF-alpha (2) at high concentrations, it induces apoptosis in FLS. Simvastatin 127-138 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 18006645-5 2008 Moreover, exogenously applied LPA induces FLS migration and secretion of IL-8/IL-6, whereas the LPA(3) agonist l-sn-1-O-oleoyl-2-methyl-glyceryl-3-phosphothionate (2S-OMPT) stimulates cytokine synthesis but not cell motility. lysophosphatidic acid 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 17941093-9 2008 IL-8 release was mediated by extracellular-regulated kinase (ERK) and p38 mitogen-activated protein kinase (MAPK) and inhibited by mesalamine, but not hydrocortisone, at therapeutic concentrations. Hydrocortisone 151-165 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 17941093-12 2008 The IL-8 release is MAPK-dependent and inhibited by mesalamine. Mesalamine 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 18303186-6 2008 Kinetic studies revealed that TNF-alpha and IL-8 release occurred in a time-dependent manner with release of two cytokines beginning at 3 hr post-exposure to well-known haptens, DNCB and NiSO(4). Dinitrochlorobenzene 178-182 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 18303186-6 2008 Kinetic studies revealed that TNF-alpha and IL-8 release occurred in a time-dependent manner with release of two cytokines beginning at 3 hr post-exposure to well-known haptens, DNCB and NiSO(4). niso 187-191 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17962359-7 2008 CaSR stimulation by extracellular calcium or agonists, such as spermine or Mg(2+), caused ERK1 and 2 activation, intracellular calcium concentration ([Ca(2+)](i)) mobilization (as assessed by microspecfluorometry using Fluo-4), and secretion of the multifunctional cytokine IL-8 (CX-CL8). Calcium 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 274-278 18069112-1 2008 Sodium fluoride (NaF) has been shown to be cytotoxic and produces inflammatory responses in humans. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 18607954-1 2008 CONCLUSIONS: The results suggest that the anti-inflammatory effect of caffeic acid phenethyl ester (CAPE) is due to its inhibition of tumor necrosis factor (TNF)-alpha expression and interleukin (IL)-8 production. caffeic acid phenethyl ester 70-98 C-X-C motif chemokine ligand 8 Homo sapiens 183-201 18607954-1 2008 CONCLUSIONS: The results suggest that the anti-inflammatory effect of caffeic acid phenethyl ester (CAPE) is due to its inhibition of tumor necrosis factor (TNF)-alpha expression and interleukin (IL)-8 production. caffeic acid phenethyl ester 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 183-201 18717605-6 2008 Following treatment with dacarbazine, melanoma cells activate the extracellular signal-regulated kinase pathway, which results in over-expression and secretion of interleukin (IL)-8 and vascular endothelial growth factor. Dacarbazine 25-36 C-X-C motif chemokine ligand 8 Homo sapiens 163-181 17947611-3 2008 Macrolide antibiotics, such as clarithromycin, have in vitro efficacy against IL-8 and neutrophils, key inflammatory mediators in noneosinophilic asthma. macrolide antibiotics 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 17947611-3 2008 Macrolide antibiotics, such as clarithromycin, have in vitro efficacy against IL-8 and neutrophils, key inflammatory mediators in noneosinophilic asthma. Clarithromycin 31-45 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 17947611-9 2008 Clarithromycin therapy significantly reduced airway concentrations of IL-8 and neutrophil numbers and improved quality-of-life scores compared with placebo. Clarithromycin 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17947611-12 2008 CONCLUSIONS: Clarithromycin therapy can modulate IL-8 levels and neutrophil accumulation and activation in the airways of patients with refractory asthma. Clarithromycin 13-27 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 18497054-5 2008 Treatment with the tyrosine kinase inhibitor gefitinib (Iressa) returned the expression levels of IL-8 and GRO back to the baseline observed in HER2-negative MCF-7 BC cells. Gefitinib 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 19051345-6 2008 Analysis of the anti-inflammatory effects of ursolic acid and oleanolic acid, the triterpene compounds present in PPY, showed that ursolic acid significantly inhibited LPS-induced IL-8 production, NF-kappaB activation, and iNOS mRNA expression, whereas oleanolic acid did not have these effects. Oleanolic Acid 62-76 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 19051345-6 2008 Analysis of the anti-inflammatory effects of ursolic acid and oleanolic acid, the triterpene compounds present in PPY, showed that ursolic acid significantly inhibited LPS-induced IL-8 production, NF-kappaB activation, and iNOS mRNA expression, whereas oleanolic acid did not have these effects. ursolic acid 131-143 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 17962359-7 2008 CaSR stimulation by extracellular calcium or agonists, such as spermine or Mg(2+), caused ERK1 and 2 activation, intracellular calcium concentration ([Ca(2+)](i)) mobilization (as assessed by microspecfluorometry using Fluo-4), and secretion of the multifunctional cytokine IL-8 (CX-CL8). Calcium 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 280-286 17962359-7 2008 CaSR stimulation by extracellular calcium or agonists, such as spermine or Mg(2+), caused ERK1 and 2 activation, intracellular calcium concentration ([Ca(2+)](i)) mobilization (as assessed by microspecfluorometry using Fluo-4), and secretion of the multifunctional cytokine IL-8 (CX-CL8). Spermine 63-71 C-X-C motif chemokine ligand 8 Homo sapiens 274-278 17962359-7 2008 CaSR stimulation by extracellular calcium or agonists, such as spermine or Mg(2+), caused ERK1 and 2 activation, intracellular calcium concentration ([Ca(2+)](i)) mobilization (as assessed by microspecfluorometry using Fluo-4), and secretion of the multifunctional cytokine IL-8 (CX-CL8). Spermine 63-71 C-X-C motif chemokine ligand 8 Homo sapiens 280-286 18079439-3 2008 The NO synthase inhibitor N(G)-nitro-l-arginine methyl ester (L-NAME) significantly (P < 0.001) enhanced IL-8-induced migration by up to 45%. NG-Nitroarginine Methyl Ester 26-60 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 17962359-7 2008 CaSR stimulation by extracellular calcium or agonists, such as spermine or Mg(2+), caused ERK1 and 2 activation, intracellular calcium concentration ([Ca(2+)](i)) mobilization (as assessed by microspecfluorometry using Fluo-4), and secretion of the multifunctional cytokine IL-8 (CX-CL8). magnesium ion 75-81 C-X-C motif chemokine ligand 8 Homo sapiens 274-278 18079439-3 2008 The NO synthase inhibitor N(G)-nitro-l-arginine methyl ester (L-NAME) significantly (P < 0.001) enhanced IL-8-induced migration by up to 45%. NG-Nitroarginine Methyl Ester 62-68 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 18079439-5 2008 Antibodies to L-selectin or PSGL-1 had no effect on IL-8-induced migration but prevented the increased migration to IL-8 induced by L-NAME. NG-Nitroarginine Methyl Ester 132-138 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 17962359-7 2008 CaSR stimulation by extracellular calcium or agonists, such as spermine or Mg(2+), caused ERK1 and 2 activation, intracellular calcium concentration ([Ca(2+)](i)) mobilization (as assessed by microspecfluorometry using Fluo-4), and secretion of the multifunctional cytokine IL-8 (CX-CL8). magnesium ion 75-81 C-X-C motif chemokine ligand 8 Homo sapiens 280-286 18079439-8 2008 Only microparticles from L-NAME and not untreated or D-NAME-treated neutrophils induced a significant (P < 0.01) increase in IL-8-induced migration and transendothelial migration. NG-Nitroarginine Methyl Ester 25-31 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 18006311-1 2008 A series of novel and potent 3,4-diamino-2,5-thiadiazole-1-oxides were prepared and found to show excellent binding affinities for CXCR2 and CXCR1 receptors and excellent inhibitory activity of Gro-alpha and IL-8 mediated in vitro hPMN MPO release of CXCR2 and CXCR1 expressing cell lines. 3,4-diamino-2,5-thiadiazole-1-oxides 29-65 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 17405871-7 2008 The cord blood cortisol concentration was significantly increased in the presence of chorioamnionitis or funisitis and was moderately correlated with cord blood IL6 (r = 0.64, p<0.01) and IL8 (r = 0.52, p<0.01). Hydrocortisone 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 191-194 18023202-0 2008 IL-8 induces imbalances between nitric oxide and endothelin-1, and also between plasminogen activator inhibitor-1 and tissue-type plasminogen activator in cultured endothelial cells. Nitric Oxide 32-44 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18781069-1 2008 BACKGROUND: Large increases in salivary fluoride were reported 1 h after a calcium pre-rinse/NaF rinse. salivary fluoride 31-48 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 18639962-11 2008 Inhibition of ERK1/2, JNK1/2 and p38 MAPK with PD98059, SP600125 and SB203580, respectively, led to the suppression of the shear stress-induced IL-8 gene expression (P<0.01), which was also blocked by JNK1/2 siRNA (small interfering RNA) (P<0.01). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 47-54 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 18639962-11 2008 Inhibition of ERK1/2, JNK1/2 and p38 MAPK with PD98059, SP600125 and SB203580, respectively, led to the suppression of the shear stress-induced IL-8 gene expression (P<0.01), which was also blocked by JNK1/2 siRNA (small interfering RNA) (P<0.01). pyrazolanthrone 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 18639962-11 2008 Inhibition of ERK1/2, JNK1/2 and p38 MAPK with PD98059, SP600125 and SB203580, respectively, led to the suppression of the shear stress-induced IL-8 gene expression (P<0.01), which was also blocked by JNK1/2 siRNA (small interfering RNA) (P<0.01). SB 203580 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 17725646-4 2008 A S. Typhi tviABCDEvexABCDE deletion mutant, but not a tviBCDEvexABCDE deletion mutant, elicited increased IL-8 production, which could be reduced to wild-type levels by introducing the cloned tviA regulatory gene. tviabcdevexabcde 11-27 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 17725646-8 2008 Introduction of tviA into S. enterica serotype Typhimurium reduced flagellin secretion and IL-8 expression. tvia 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 19364068-9 2008 Decreased MCP-1, IL-6, and IL-8 expression indicated that APS-purified islets were possibly exposed to less proinflammatory stress. aps 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 18180640-13 2008 After exposure to morphine sulfate, adult neutrophils showed no difference in IL-8 receptor expression, whereas newborn neutrophils expressed fewer IL-8 receptors. Morphine 18-34 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 18180640-16 2008 The differential effect may be explained in part by the reduction of IL-8 receptors of newborn neutrophils after morphine exposure. Morphine 113-121 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 18854128-10 2008 348 kPa) moduli IPN surfaces attenuated IL-8 secretion. ipn 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 18472047-7 2008 Results showed that ATP decreased the rise in concentrations of TNF-alpha, interferon-gamma (IFN-gamma) and IL-1beta, but increased concentrations of IL-8 and IL-10. Adenosine Triphosphate 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 18668392-8 2008 Dexamethasone enhanced IL-10 (p = 0.013) and suppressed IL-1beta, TNF-alpha, interleukin 6 (IL-6), and interleukin 8 (IL-8) (p = 0.013). Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 103-116 18668392-8 2008 Dexamethasone enhanced IL-10 (p = 0.013) and suppressed IL-1beta, TNF-alpha, interleukin 6 (IL-6), and interleukin 8 (IL-8) (p = 0.013). Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 18488441-9 2008 Sputum supernatant IL-8 correlated with total neutrophil count per gram of sputum (r = 0.52, p = 0.04) and with EBC pH (r = -0.59, p = 0.02). NSC638702 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 17965029-6 2008 A significant inhibitory effect of besifloxacin was observed at 0.1 mg/L for IL-1alpha, at 1 mg/L for G-CSF, IL-1ra and IL-6 and at 30 mg/L for GM-CSF, IL-12p40, IL-1beta, IL-8, IP-10, MCP-1 and MIP-1alpha. besifloxacin 35-47 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 17707405-6 2008 RESULTS: The IL-8 production by the HUVECs was significantly higher in the high glucose culture than in the control culture (glucose concentration of 100 mg/dL) (P < 0.05). Glucose 80-87 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 18447141-8 2008 These results support previous data suggesting an important role for IL-8 and drug-specific T cells in the pathogenesis ofAGEP and imply that the reaction was specific to tetrazepam with no cross-reactivity to other benzodiazepines. tetrazepam 171-181 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 18077529-1 2008 Although (18)F-labeled NaF was the first widely used agent for skeletal scintigraphy, it quickly fell into disuse after the introduction of (99m)Tc-labeled bone-imaging agents. Fluorine 13-14 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 17541958-7 2008 CS also increased the phosphorylation of MAPK"s and the production of IL-8 but interestingly only in stimulated cells. Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17947496-5 2008 Treatment of cells with 20-HETE markedly increased levels of prostaglandin (PG) E(2) and 8-epi-isoprostane PGF(2alpha), commonly used markers of activation and oxidative stress, and most prominently, interleukin-8, a potent neutrophil chemotactic factor whose overproduction by the endothelium is a key feature of vascular injury. 20-Hete 24-31 C-X-C motif chemokine ligand 8 Homo sapiens 200-213 17707405-6 2008 RESULTS: The IL-8 production by the HUVECs was significantly higher in the high glucose culture than in the control culture (glucose concentration of 100 mg/dL) (P < 0.05). Glucose 125-132 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 17707405-7 2008 Moreover, the hyperglycemia associated with elevated TNF-alpha was found to enhance the level of IL-8 production by the HUVECs cultured at all glucose concentrations and over both time courses, compared to the control (P < 0.05). Glucose 143-150 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 18227044-0 2008 [Effect of glutamine on serum interleukin-8 and tumor necrosis factor-alpha levels in patients with severe pancreatitis]. Glutamine 11-20 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 18052220-6 2008 In the presence of NaF, hydroxyl radicals were detected by an ethanol scavenger, whereas such radicals were not found in the absence of NaF. Hydroxyl Radical 24-41 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 18052220-6 2008 In the presence of NaF, hydroxyl radicals were detected by an ethanol scavenger, whereas such radicals were not found in the absence of NaF. Ethanol 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 18227044-1 2008 OBJECTIVE: To observe the changes in serum interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha) after intravenous administration of alanyl-glutamine (Gln) in patients with severe pancreatitis. alanylglutamine 144-160 C-X-C motif chemokine ligand 8 Homo sapiens 43-56 18227044-1 2008 OBJECTIVE: To observe the changes in serum interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha) after intravenous administration of alanyl-glutamine (Gln) in patients with severe pancreatitis. alanylglutamine 144-160 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 18227044-1 2008 OBJECTIVE: To observe the changes in serum interleukin-8 (IL-8) and tumor necrosis factor-alpha (TNF-alpha) after intravenous administration of alanyl-glutamine (Gln) in patients with severe pancreatitis. alanylglutamine 162-165 C-X-C motif chemokine ligand 8 Homo sapiens 43-56 18227044-4 2008 RESULTS: On day of Gln administration, the plasma glutamine level in patients of Gln group increased significantly (P<0.01), and serum IL-8 and TNF-alpha levels decreased significantly (P>0.05) in comparison with those of the control group. alanylglutamine 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 18227044-6 2008 CONCLUSION: Gln-enriched TPN may improve the clinical outcomes of patients with severe pancreatitis probably by decreasing serum IL-8 and TNF-alpha levels. alanylglutamine 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 19001760-0 2008 [Anti-fungal drug liranaftate suppresses fungal element-promoted production of IL-8 in normal human keratinocytes]. liranaftate 18-29 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 18332643-3 2008 OBJECTIVES: We hypothesize that end-tidal carbon monoxide corrected for inhaled CO (ETCOc), malondialdehyde (MDA) (markers of oxidative stress) and proinflammatory cytokine (IL-6, IL-8) production are higher in infants of preeclamptic mothers with HELLP syndrome than in those of preeclamptic mothers without HELLP syndrome. Carbon Monoxide 42-57 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 17716784-4 2008 Under certain conditions, however, stress hormones, substance P, ATP and the activation of the corticotropin-releasing hormone/substance P-histamine axis may actually facilitate inflammation, through induction of interleukin (IL)-1, IL-6, IL-8, IL-18, tumor necrosis factor (TNF)-alpha and CRP production. Histamine 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 19001760-3 2008 The fungal elements beta-D-glucan and trichophytin from Trichophyton rubrum and Trichophyton mentagrophytes augmented production of IL-8 and IL-1 alpha of cultured normal human epidermal keratinocytes. maltotriose 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 19001760-5 2008 Next we examined the effect of liranaftate, a representative Japanese thiocarbamate antifungal agent, on the production of IL-8 and IL-1 alpha. liranaftate 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 19001760-7 2008 Augmented production of IL-8 was profoundly suppressed by the addition of liranaftate to the culture in a dose-dependent manner. liranaftate 74-85 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 19001760-8 2008 Clinically, liranaftate an antifungal drug with IL-8-decreasing activity may reduce infiltration of neutrophils in the skin and their invasion into the epidermis. liranaftate 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 18946510-6 2008 Applying a whole blood assay, IC(50) values of pro-inflammatory cytokine release (TNF-alpha, IL-6, IL-8, IL-1beta) were found to be positively correlated with the K(i)-values of the aforementioned polyphenols. Polyphenols 197-208 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 19119578-1 2008 PURPOSE: To clinically evaluate the additional effect of adding 0.12% chlorhexidine digluconate (CHX) to a 0.05% sodium fluoride (NaF) mouth rinse in arresting active enamel caries lesions after 28 days. Sodium Fluoride 113-128 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 18846238-6 2008 Increases in H2O2 heavily contributed to the excessive IL-6 and IL-8 production in CF epithelia. Hydrogen Peroxide 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 18677938-1 2008 UNLABELLED: The aim of our study was to characterize the priming effect of extracellular nucleotides on reactive oxygen species (ROS) production induced by formyl-methionyl-leucyl-phenylalanine (fMLP), interleukin-8 (IL-8), leukotriene B4 (LTB4), and platelet activating factor (PAF). Reactive Oxygen Species 104-127 C-X-C motif chemokine ligand 8 Homo sapiens 202-215 18846238-8 2008 When cells are stimulated, differential expression in CF versus normal is enhanced; corresponding to an increase in H2O2 mediated production of IL-6 and IL-8. Hydrogen Peroxide 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 18846238-11 2008 We conclude that a paradoxical decrease in Nrf-2 driven antioxidant responses in CF epithelia results in an increase in steady state H2O2, which in turn contributes to the overproduction of the pro-inflammatory cytokines IL-6 and IL-8. Hydrogen Peroxide 133-137 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 17692547-0 2008 Fluticasone, but not salmeterol, reduces cigarette smoke-induced production of interleukin-8 in human airway smooth muscle. Fluticasone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 17692547-3 2008 We have investigated the effect of fluticasone propionate, a corticosteroid, and salmeterol, a beta 2-adrenergic receptor agonist, on cigarette smoke extract-induced IL-8 production by human airway smooth muscle cells. Salmeterol Xinafoate 81-91 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 17692547-6 2008 Fluticasone dose-dependently inhibited IL-8 release induced by cigarette smoke extract, TNFalpha or combined cigarette smoke extract and TNFalpha. Fluticasone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 17692547-7 2008 However, while IL-8 release in the presence of cigarette smoke extract alone was completely inhibited by fluticasone, IL-8 production induced by cigarette smoke extract and TNFalpha was only partially reduced. Fluticasone 105-116 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 17692547-10 2008 Fluticasone but not salmeterol is effective in reducing cigarette smoke extract-induced IL-8 production in human airway smooth muscle cells. Fluticasone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 17692547-11 2008 The reduced inhibition of cigarette smoke extract- and TNFalpha-induced IL-8 release by fluticasone may explain why corticosteroids are less effective in chronic obstructive pulmonary disease where increased amounts of TNFalpha are present. Fluticasone 88-99 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 17202807-9 2008 IL-8 levels in the supernatant obtained from SAEC cultures were increased following the addition of beta-D-glucan in vitro. maltotriose 100-113 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18677938-11 2008 Rottlerin (5 microM), a PKC delta inhibitor, almost abolished the effect of fMLP in the absence or in the presence of UTP, indicating that PKC delta is essential for the fMLP-induced effect; rottlerin also caused inhibition of ROS production induced by IL-8, LTB4 or PAF, however the priming effect of UTP was not affected for these chemoattractants. rottlerin 191-200 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 18677938-1 2008 UNLABELLED: The aim of our study was to characterize the priming effect of extracellular nucleotides on reactive oxygen species (ROS) production induced by formyl-methionyl-leucyl-phenylalanine (fMLP), interleukin-8 (IL-8), leukotriene B4 (LTB4), and platelet activating factor (PAF). Reactive Oxygen Species 104-127 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 18677938-1 2008 UNLABELLED: The aim of our study was to characterize the priming effect of extracellular nucleotides on reactive oxygen species (ROS) production induced by formyl-methionyl-leucyl-phenylalanine (fMLP), interleukin-8 (IL-8), leukotriene B4 (LTB4), and platelet activating factor (PAF). Reactive Oxygen Species 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 202-215 18677938-1 2008 UNLABELLED: The aim of our study was to characterize the priming effect of extracellular nucleotides on reactive oxygen species (ROS) production induced by formyl-methionyl-leucyl-phenylalanine (fMLP), interleukin-8 (IL-8), leukotriene B4 (LTB4), and platelet activating factor (PAF). Reactive Oxygen Species 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 18677938-9 2008 GF 109203X (5 microM), an inhibitor of all neutrophil"s PKC isoforms, or RO 31-8220 (5uM), an inhibitor of classical and novel PKC isoforms, abolished the responses induced by fMLP (10 nM) IL-8 (10 nM), LTB4 (100 nM) or PAF (100 nM). bisindolylmaleimide I 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 18677938-11 2008 Rottlerin (5 microM), a PKC delta inhibitor, almost abolished the effect of fMLP in the absence or in the presence of UTP, indicating that PKC delta is essential for the fMLP-induced effect; rottlerin also caused inhibition of ROS production induced by IL-8, LTB4 or PAF, however the priming effect of UTP was not affected for these chemoattractants. rottlerin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 17471497-1 2007 We have shown that the bacterial iron chelator, deferoxamine (DFO), triggers inflammatory signals including the production of CXC chemokine IL-8, in human intestinal epithelial cells (IECs) by activating the ERK1/2 and p38 kinase pathways. Deferoxamine 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 17996682-4 2007 We thus examined the independent contributions of the bovine-human-discrepant amino acids within CXCL8 to the biological activity of bG31P. bg31p 133-138 C-X-C motif chemokine ligand 8 Homo sapiens 97-102 17996682-5 2007 We first examined the effect of wholesale ligation of the carboxy half of hCXCL8 onto the amino half of bG31P, and found that this human-bovine chaemeric G31P (hbG31P; i.e., bCXCL8((3-44))K11R/G31P-hCXCL8((45-72))) fully retained the ELR-CXC chemokine antagonist activity of bG31P. bg31p 161-166 C-X-C motif chemokine ligand 8 Homo sapiens 74-80 17996682-6 2007 Thus, hbG31P blocked the abilities of human CXCL8 to chemoattract human neutrophil or induce reactive oxygen intermediate (ROI) release. reactive oxygen 93-108 C-X-C motif chemokine ligand 8 Homo sapiens 44-49 17471497-0 2007 Transcriptional regulation of IL-8 by iron chelator in human epithelial cells is independent from NF-kappaB but involves ERK1/2- and p38 kinase-dependent activation of AP-1. Iron 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 17471497-2 2007 In this study we investigated the mechanisms involved in IL-8 generation by DFO, focusing on the transcription factors involved and the roles of both mitogen-activated protein kinases (MAPKs) in the transcription factor activation. Deferoxamine 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 17471497-1 2007 We have shown that the bacterial iron chelator, deferoxamine (DFO), triggers inflammatory signals including the production of CXC chemokine IL-8, in human intestinal epithelial cells (IECs) by activating the ERK1/2 and p38 kinase pathways. Iron 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 17471497-9 2007 In summary, our results indicate that iron chelator-induced IL-8 generation in IECs involves activation of ERK1/2 and p38 kinase and downstream activation of AP-1. Iron 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 17471497-1 2007 We have shown that the bacterial iron chelator, deferoxamine (DFO), triggers inflammatory signals including the production of CXC chemokine IL-8, in human intestinal epithelial cells (IECs) by activating the ERK1/2 and p38 kinase pathways. Deferoxamine 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 18032608-7 2007 We found that pretreatment with muramyl dipeptide (MDP), a ligand for Nod2, significantly decreased production of the proinflammatory cytokines TNF-alpha, IL-8, and IL-1beta upon Nod2, TLR4, and TLR2 restimulation in primary human monocyte-derived macrophages from a large cohort of individuals. Acetylmuramyl-Alanyl-Isoglutamine 32-49 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 17928431-5 2007 Ten times more of the synthetic structures with four to six d-alanine-substituted polyglycerophosphate units (50 nM) than of the native LTA preparation was required to induce IL-8 release. dalbergioidin 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 18071264-6 2007 LR inhibited the PMA plus A23187-induced increase in IL-6, IL-8, and TNF-alpha expression in HMC-1 cells. Calcimycin 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 17928431-5 2007 Ten times more of the synthetic structures with four to six d-alanine-substituted polyglycerophosphate units (50 nM) than of the native LTA preparation was required to induce IL-8 release. polyglycerophosphate 82-102 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 18045955-11 2007 High levels of CXCL8, CXCL1, and CXCL3 accounted for a shorter relapse-free survival of ERalpha-positive patients treated with tamoxifen. Tamoxifen 127-136 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 17455223-2 2007 Our recent study showed that ghrelin could stimulate protein kinase C-mediated activation of nuclear factor-kappaB (NF-kappaB) and interleukin-8 secretion in human colonic epithelial cells transfected with a functional ghrelin receptor. Ghrelin 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 131-144 17961179-0 2007 Heparin-induced thrombocytopenia associated with interleukin-8-dependent platelet activation in a patient with antiphospholipid syndrome. Heparin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 17961179-3 2007 Further analysis revealed anti-interleukin (IL)-8 antibodies and IL-8-dependent platelet activation facilitated by heparin, which may explain this unusual case of heparin-induced thrombocytopenia. Heparin 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 17961179-3 2007 Further analysis revealed anti-interleukin (IL)-8 antibodies and IL-8-dependent platelet activation facilitated by heparin, which may explain this unusual case of heparin-induced thrombocytopenia. Heparin 163-170 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 17922819-11 2007 At 72 h the trilayer severely restricted transfer of sodium fluorescein (NaF) (ten-fold reduction) whilst transfer of a 4 kDa FITC-conjugated dextran was virtually occluded, confirming a restrictive barrier. Fluorescein 53-71 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 17908789-0 2007 Functional analysis of KSRP interaction with the AU-rich element of interleukin-8 and identification of inflammatory mRNA targets. Gold 49-51 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 18085018-3 2007 The most prominent effect of macrolides noted in vitro is the inhibition of pro-inflammatory cytokines such as interleukin-8. Macrolides 29-39 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 17923111-5 2007 Moreover, LPA1 and LPA3 siRNA also inhibited LPA-enhanced IL-1-dependent long-term IL-8 and MCP-1 mRNA expression, and subsequent THP-1 cell chemotaxis toward LPA-treated HUVEC-conditioned media. lysophosphatidic acid 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 17720209-11 2007 Preincubation with intracellular calcium chelator (BAPTA-AM) attenuated IL-1beta and IL-8 production, but not GM-CSF and LIF production. Calcium 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17720209-11 2007 Preincubation with intracellular calcium chelator (BAPTA-AM) attenuated IL-1beta and IL-8 production, but not GM-CSF and LIF production. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17720209-13 2007 Our results also suggest that PM(10) induces the production of pro-inflammatory mediators via either intracellular calcium-dependent (IL-1beta, IL-8) or -independent (GM-CSF, LIF) pathways. Calcium 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 17923111-5 2007 Moreover, LPA1 and LPA3 siRNA also inhibited LPA-enhanced IL-1-dependent long-term IL-8 and MCP-1 mRNA expression, and subsequent THP-1 cell chemotaxis toward LPA-treated HUVEC-conditioned media. lysophosphatidic acid 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 18039378-12 2007 BES released the inflammatory mediators IL-8, PGE2 and LTB4 constitutively and following exposure to LPS. BES 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17897621-5 2007 In contrast, the STS-induced ATP increase was prevented by any of three inhibitors of the glycolytic pathway: 2-deoxyglucose, iodoacetamide, and NaF. Adenosine Triphosphate 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 145-148 18039378-13 2007 Interestingly, LPS induced a higher release of IL-8, but not PGE2 and LTB4 in COPD BES (p < 0.001) which correlated with lung function changes. BES 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 17643414-6 2007 In addition, flavone was found to reduce the lipopolysaccharide (LPS)-induced interleukin (IL)-8 production in pulmonary epithelial cells, which was confirmed by transcription analysis. flavone 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 78-96 17533374-9 2007 Finally, inhibition of IL-8 signaling potentiated etoposide-induced cell death in hypoxic PC3 cells. Etoposide 50-59 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 17977560-2 2007 Butein significantly inhibited TNF-alpha-induced interleukin 8 (IL-8) secretion and mRNA expression. butein 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 17977560-2 2007 Butein significantly inhibited TNF-alpha-induced interleukin 8 (IL-8) secretion and mRNA expression. butein 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 18323243-1 2007 The interactions in free radicals processes between cyclosporine A (CsA) and sodium fluoride (NaF) on in vitro model human placental mitochondria were evaluated. Sodium Fluoride 77-92 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 17720876-6 2007 A 5-10% dilution of FLDE stimulated a significant release of IL-6 and IL-8 at 6-24 h in a PKC-dependent manner vs. control medium-treated cells. flde 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17600310-5 2007 By gas chromatography/mass spectrometry (GC/MS) we show that acrolein and crotonaldehyde, two alpha,beta-unsaturated aldehydes, are contained in aqueous cigarette smoke extract (CSE) at micromolar concentrations and mimic CSE in evoking the release of the neutrophil chemoattractant IL-8 and of the pleiotropic inflammatory cytokine TNF-alpha from the human macrophagic cell line U937. Acrolein 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 283-287 17600310-5 2007 By gas chromatography/mass spectrometry (GC/MS) we show that acrolein and crotonaldehyde, two alpha,beta-unsaturated aldehydes, are contained in aqueous cigarette smoke extract (CSE) at micromolar concentrations and mimic CSE in evoking the release of the neutrophil chemoattractant IL-8 and of the pleiotropic inflammatory cytokine TNF-alpha from the human macrophagic cell line U937. 2-butenal 74-88 C-X-C motif chemokine ligand 8 Homo sapiens 283-287 17600310-6 2007 In addition, acrolein (10-30 microM) released IL-8 also from cultured human alveolar macrophages and THP-1 macrophagic cells. Acrolein 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 17600310-7 2007 4-hydroxy-2-nonenal (30-100 microM), an endogenous alpha,beta-unsaturated aldehyde that is abundant in lungs of patients with COPD, stimulated the release of IL-8 from U937 cells, whereas the saturated aldehyde, acetaldehyde, was ineffective. 4-hydroxy-2-nonenal 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 17600310-7 2007 4-hydroxy-2-nonenal (30-100 microM), an endogenous alpha,beta-unsaturated aldehyde that is abundant in lungs of patients with COPD, stimulated the release of IL-8 from U937 cells, whereas the saturated aldehyde, acetaldehyde, was ineffective. alpha,beta-unsaturated aldehyde 51-82 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 17600310-7 2007 4-hydroxy-2-nonenal (30-100 microM), an endogenous alpha,beta-unsaturated aldehyde that is abundant in lungs of patients with COPD, stimulated the release of IL-8 from U937 cells, whereas the saturated aldehyde, acetaldehyde, was ineffective. Aldehydes 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 17600310-7 2007 4-hydroxy-2-nonenal (30-100 microM), an endogenous alpha,beta-unsaturated aldehyde that is abundant in lungs of patients with COPD, stimulated the release of IL-8 from U937 cells, whereas the saturated aldehyde, acetaldehyde, was ineffective. Acetaldehyde 212-224 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 17600310-8 2007 CSE-evoked IL-8 release was remarkably (> 80%) inhibited by N-acetyl-cysteine (0.1-3 mM) or glutathione monoethyl ester (1-3 mM). Acetylcysteine 63-80 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 17600310-8 2007 CSE-evoked IL-8 release was remarkably (> 80%) inhibited by N-acetyl-cysteine (0.1-3 mM) or glutathione monoethyl ester (1-3 mM). S-ethyl glutathione 95-122 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 17720876-9 2007 However, the PKCepsilon inhibitor, Ro 31-8220, effectively inhibited FLDE-stimulated IL-8 and IL-6 release. Ro 31-8220 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17720876-9 2007 However, the PKCepsilon inhibitor, Ro 31-8220, effectively inhibited FLDE-stimulated IL-8 and IL-6 release. flde 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17720876-10 2007 Inhibition of FLDE-stimulated IL-6 and IL-8 was confirmed in a dominant-negative PKCepsilon-expressing BEAS-2B cell line but not observed in a PKCalpha dominant negative BEAS-2B cell line. flde 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 17720876-11 2007 These data support the hypothesis that FLDE exposure stimulates bronchial epithelial IL-8 and IL-6 release via a PKCepsilon-dependent pathway. flde 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17891168-10 2007 The anti-inflammatory glucocorticoid, dexamethasone, inhibited the histamine enhanced NF-kappaB-dependent transcription and IL-6 and IL-8 release. Dexamethasone 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 17916596-10 2007 TNF-alpha-induced up-regulation of IL-8 via nuclear factor-kappaB in CAFs is an inflammatory pathway, potentially permissive for cancer invasion that may represent a novel therapeutic target. cafs 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 18201443-7 2007 RESULTS: In primary HSNEC, IL-8 mRNA levels decreased dose dependently in the range of 10-50 microM of AC with an eightfold decrease at 50 microM. Acrolein 103-105 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 18201443-10 2007 However, differentiated HSNEC showed a marginal decrease in a dose-dependent manner for both IL-8 and HBD-2 within the range of 10-50 microM of AC. Acrolein 144-146 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 17891168-7 2007 The H(1) receptor antagonist, mepyramine, caused a rightward shift in the concentration-response curves of TNFalpha-induced NF-kappaB-dependent transcription (pA(2)=9.91) and release of IL-6 (pA(2)=8.78) and IL-8 (pA(2)=8.99). Pyrilamine 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 17891168-10 2007 The anti-inflammatory glucocorticoid, dexamethasone, inhibited the histamine enhanced NF-kappaB-dependent transcription and IL-6 and IL-8 release. Histamine 67-76 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 17761353-7 2007 Taken together, these results suggest that HPE-induced IL-8 secretion occurs via activation of JNK/SAPK and transcription factors NF-kappaB and AP-1 in PMA-differentiated THP-1 cells. 1-(3-Methoxy-4-hydroxyphenyl)-2-[2-hydroxy-3-methoxy-5-[4-(3-methoxy-4-hydroxyphenyl)-3,7-dioxabicyclo[3.3.0]octane-8-yl]phenyl]-3-hydroxy-1-propanone 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 17767946-5 2007 Removal of gas phase and a portion of the particle phase hydrocarbons with the denuder decreased the interleukin-8 (IL-8) secretion to unexposed levels. Hydrocarbons 57-69 C-X-C motif chemokine ligand 8 Homo sapiens 101-114 17767946-5 2007 Removal of gas phase and a portion of the particle phase hydrocarbons with the denuder decreased the interleukin-8 (IL-8) secretion to unexposed levels. Hydrocarbons 57-69 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 17877767-9 2007 CONCLUSION: Differential effects on MC cytokine inhibition were observed, with epinastine inhibiting MC secretion of IL-5, IL-8, IL-10 and conjunctival neutrophil infiltration. epinastine 79-89 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 17959901-4 2007 Stimulation of gingival fibroblasts with tumor necrosis factor-alpha, IL-1alpha, and lipopolysaccharide markedly induced IL-8 production, and the IL-8 production was synergistically augmented in the presence of or pre-treatment with histamine. Histamine 233-242 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 17959901-6 2007 These results indicate that histamine induces IL-8 production from gingival fibroblasts through H1R, and synergistically augments the inflammatory stimuli by amplification of the MAPK and NF-kappaB through H1R-linked PLC. Histamine 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 17947704-4 2007 In this study, we demonstrate that 17beta-estradiol (E2) attenuates LPS-induced expression of CXCL8 in human peripheral blood monocytes. Estradiol 35-51 C-X-C motif chemokine ligand 8 Homo sapiens 94-99 17684042-5 2007 fMLF, IL-8, leukotriene B(4), or platelet-activating factor stimulation resulted in an initial increase in VASP Ser 157 phosphorylation, which was maximal by 30 s and was followed by a return to baseline Ser 157 phosphorylation by 10 min. Serine 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 17684042-5 2007 fMLF, IL-8, leukotriene B(4), or platelet-activating factor stimulation resulted in an initial increase in VASP Ser 157 phosphorylation, which was maximal by 30 s and was followed by a return to baseline Ser 157 phosphorylation by 10 min. Serine 204-207 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 17947704-5 2007 Treatment of monocytes with estradiol before administration of LPS reduces CXCL8 message and protein production through an estrogen receptor-dependent mechanism, and luciferase reporter assays demonstrate that this inhibition is mediated transcriptionally. Estradiol 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 75-80 17805211-0 2007 Butyrate regulates the expression of pathogen-triggered IL-8 in intestinal epithelia. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 17639599-13 2007 High glucose-induced IL-8 production by microglia may contribute to diabetic encephalopathy. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 18035981-10 2007 This fact indicates that the chemokine pathway of IL-8 activity could be modulated by this treatment, most likely by polycyclic aromatic hydrocarbons. Polycyclic Aromatic Hydrocarbons 117-149 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 17639599-4 2007 Therefore, we investigated whether high glucose could activate microglia and stimulate IL-8 secretion and if so, the possible mechanisms that were involved. Glucose 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 17639599-5 2007 ELISA results showed that treatment with high glucose (35 mM) compared with treatment with low glucose (10 mM) time-dependently elevated secretion of GRO (the rat ortholog of human IL-8) in primary cultured rat microglia. Glucose 46-53 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 17639599-5 2007 ELISA results showed that treatment with high glucose (35 mM) compared with treatment with low glucose (10 mM) time-dependently elevated secretion of GRO (the rat ortholog of human IL-8) in primary cultured rat microglia. Glucose 95-102 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 17805211-6 2007 Butyrate transiently down-regulated expression of IL-8 stimulated by Pam3CSK4. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 17805211-7 2007 Treatment of cells with butyrate before Pam3CSK4, however, enhanced production of IL-8. Butyrates 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 17964516-11 2007 Using the area under the dose response curve (AUC(0 to 24) h), thalidomide reduced the AUC for IL-6 by 56%, for IL-8 by 30%, and TNF-alpha by 32%. Thalidomide 63-74 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 17707346-0 2007 Modulation of early growth response gene 1 and interleukin-8 expression by ribotoxin deoxynivalenol (vomitoxin) via ERK1/2 in human epithelial intestine 407 cells. deoxynivalenol 85-99 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 17726017-0 2007 Role of the Jak/STAT pathway in the regulation of interleukin-8 transcription by oxidized phospholipids in vitro and in atherosclerosis in vivo. Phospholipids 90-103 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 17726017-1 2007 Oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine (Ox-PAPC) and its component phospholipid, 1-palmitoyl-2-epoxyisoprostane-sn-glycero-3-phosphorylcholine, induce endothelial cells (EC) to synthesize chemotactic factors, such as interleukin 8 (IL-8). 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine 9-66 C-X-C motif chemokine ligand 8 Homo sapiens 245-258 17726017-1 2007 Oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine (Ox-PAPC) and its component phospholipid, 1-palmitoyl-2-epoxyisoprostane-sn-glycero-3-phosphorylcholine, induce endothelial cells (EC) to synthesize chemotactic factors, such as interleukin 8 (IL-8). 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine 9-66 C-X-C motif chemokine ligand 8 Homo sapiens 260-264 17707346-0 2007 Modulation of early growth response gene 1 and interleukin-8 expression by ribotoxin deoxynivalenol (vomitoxin) via ERK1/2 in human epithelial intestine 407 cells. deoxynivalenol 101-110 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 17707346-2 2007 The purpose of this study was to test the hypothesis that ribotoxin DON evokes the epithelial sentinel signals which contributes to the pro-inflammatory cytokine interleukin-8 in human epithelial cells. ribotoxin 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 17707346-4 2007 Particularly, ribotoxin DON markedly elevated the phosphorylated extracellular signal-regulated protein kinases 1 and 2 (ERK1/2) mitogen-activated protein kinase (MAPK) which mediated DON-induced interleukin-8 (IL-8) production. DONS 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 196-209 17707346-4 2007 Particularly, ribotoxin DON markedly elevated the phosphorylated extracellular signal-regulated protein kinases 1 and 2 (ERK1/2) mitogen-activated protein kinase (MAPK) which mediated DON-induced interleukin-8 (IL-8) production. DONS 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 17707346-5 2007 DON-activated ERK1/2 also mediated the production of early growth response gene 1 (EGR-1) in the epithelial cell line and EGR-1 had the positive regulatory effect on the interleukin-8 production in the human epithelial cells. DONS 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 170-183 17883254-2 2007 Caco-2 cells were pretreated with amino acids (1, 2, and 5 mM) for 2 h and then stimulated with 1 mM H 2O 2 for 6 h. The secretion of IL-8, a proinflammatory mediator, was determined by ELISA as an indicator of tissue oxidative stress. Hydrogen Peroxide 101-107 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 17949493-2 2007 The method involves the complexation of Al, Ti and Fe with excess EDTA and the selective de-complexation of TiO-EDTA and Al-EDTA complexes with tartaric acid and NaF respectively. tio-edta 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 17949493-2 2007 The method involves the complexation of Al, Ti and Fe with excess EDTA and the selective de-complexation of TiO-EDTA and Al-EDTA complexes with tartaric acid and NaF respectively. al-edta 121-128 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Hydrogen Peroxide 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Cysteine 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Valine 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Isoleucine 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Leucine 115-118 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Tryptophan 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Histidine 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Lysine 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17883254-3 2007 The inhibition of H 2O 2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment with Cys, Val, Ile, Leu, Trp, His, Lys, and Ala. Alanine 139-142 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17631613-4 2007 Costimulation of 16HBE14o- human bronchial epithelial cells and primary mucociliary-differentiated tracheal epithelial cells with RV and TNF-alpha induced synergistic increases in IL-8 and epithelial neutrophil attractant-78 production. 16hbe14o 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 17880076-4 2007 Ranked by their propensity to orient interfacial water molecules, sodium salts could be placed in the following order: NaSCN > NaClO4 > NaI > NaNO3 approximately NaBr > NaCl > pure water approximately NaF approximately Na2SO4. sodium salts 66-78 C-X-C motif chemokine ligand 8 Homo sapiens 216-219 17683978-17 2007 The results from a partial least-square regression analysis predicted that both PAHs and a group of metals including Fe and Mn contributed to IL-6 and IL-8 induction. Iron 117-119 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 17726017-1 2007 Oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine (Ox-PAPC) and its component phospholipid, 1-palmitoyl-2-epoxyisoprostane-sn-glycero-3-phosphorylcholine, induce endothelial cells (EC) to synthesize chemotactic factors, such as interleukin 8 (IL-8). Phospholipids 95-107 C-X-C motif chemokine ligand 8 Homo sapiens 245-258 17726017-1 2007 Oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine (Ox-PAPC) and its component phospholipid, 1-palmitoyl-2-epoxyisoprostane-sn-glycero-3-phosphorylcholine, induce endothelial cells (EC) to synthesize chemotactic factors, such as interleukin 8 (IL-8). Phospholipids 95-107 C-X-C motif chemokine ligand 8 Homo sapiens 260-264 17726017-1 2007 Oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine (Ox-PAPC) and its component phospholipid, 1-palmitoyl-2-epoxyisoprostane-sn-glycero-3-phosphorylcholine, induce endothelial cells (EC) to synthesize chemotactic factors, such as interleukin 8 (IL-8). 1-palmitoyl-2-epoxyisoprostane-sn-glycero-3-phosphorylcholine 109-170 C-X-C motif chemokine ligand 8 Homo sapiens 245-258 17726017-1 2007 Oxidized 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine (Ox-PAPC) and its component phospholipid, 1-palmitoyl-2-epoxyisoprostane-sn-glycero-3-phosphorylcholine, induce endothelial cells (EC) to synthesize chemotactic factors, such as interleukin 8 (IL-8). 1-palmitoyl-2-epoxyisoprostane-sn-glycero-3-phosphorylcholine 109-170 C-X-C motif chemokine ligand 8 Homo sapiens 260-264 17917246-0 2007 Glycated human serum albumin induces interleukin 8 mRNA expression through reactive oxygen species and NADPH oxidase-dependent pathway in monocyte-derived U937 cells. Reactive Oxygen Species 75-98 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 17141246-3 2007 The objectives of this study were to examine the influence of PPAR gamma and its agonist (rosiglitazone) on the TNFalpha, IL-6, IL-8 and IL-10 gene expression in monocytes of patients with diabetic macroangiopathy and to analyse obtained results in context of selected atherogenic factors ant direct indicators of endothelial lesion. Rosiglitazone 90-103 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17141246-6 2007 Following rosiglitazone therapy, a statistically significant downward tendency of TNFalpha (p=0.026) and IL-8 (p=0.008) gene expression was noted. Rosiglitazone 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 17917246-3 2007 As a result, IL-8 mRNA expression in U-937 cells was time- and dose-dependently enhanced by stimulation with Glc-HSA and GA-HSA. glc-hsa 109-116 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 17928716-1 2007 Candida albicans, Saccharomyces cerevisiae and their cell wall components, zymosan and glucan, have been shown to stimulate interleukin-8 (IL-8/CXCL-8) production by intestinal epithelial cell-like Caco-2 cells pre-cultured with 10 mM butyric acid. Zymosan 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 17928716-1 2007 Candida albicans, Saccharomyces cerevisiae and their cell wall components, zymosan and glucan, have been shown to stimulate interleukin-8 (IL-8/CXCL-8) production by intestinal epithelial cell-like Caco-2 cells pre-cultured with 10 mM butyric acid. Glucans 87-93 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 17928716-1 2007 Candida albicans, Saccharomyces cerevisiae and their cell wall components, zymosan and glucan, have been shown to stimulate interleukin-8 (IL-8/CXCL-8) production by intestinal epithelial cell-like Caco-2 cells pre-cultured with 10 mM butyric acid. Butyric Acid 235-247 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 17917246-3 2007 As a result, IL-8 mRNA expression in U-937 cells was time- and dose-dependently enhanced by stimulation with Glc-HSA and GA-HSA. ga-hsa 121-127 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 17917246-4 2007 Furthermore, promoter activity of the IL-8 reporter gene was enhanced approximately 2-fold by stimulation with Glc-HSA and GA-HSA. Glucose 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 17917246-4 2007 Furthermore, promoter activity of the IL-8 reporter gene was enhanced approximately 2-fold by stimulation with Glc-HSA and GA-HSA. ga-hsa 123-129 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 17917246-6 2007 IL-8 mRNA expression was suppressed by NAC and apocynin but not calphostin in cells stimulated with Glc-HSA; however, its expression in cells stimulated with GA-HSA was suppressed by calphostin but not NAC. ga-hsa 158-164 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 17711515-3 2007 Neutrophils from SCD individuals showed an inhibition of spontaneous apoptosis when cultured in vitro, in the presence of autologous serum for 20 h. Intracellular cyclic adenosine monophosphate (cAMP) levels were approximately twofold increased in SCD neutrophils; possible cAMP-upregulating factors present in SCD serum include interleukin-8, granulocyte-macrophage colony-stimulating factor and prostaglandin. Cyclic AMP 163-193 C-X-C motif chemokine ligand 8 Homo sapiens 329-342 17711515-3 2007 Neutrophils from SCD individuals showed an inhibition of spontaneous apoptosis when cultured in vitro, in the presence of autologous serum for 20 h. Intracellular cyclic adenosine monophosphate (cAMP) levels were approximately twofold increased in SCD neutrophils; possible cAMP-upregulating factors present in SCD serum include interleukin-8, granulocyte-macrophage colony-stimulating factor and prostaglandin. Cyclic AMP 195-199 C-X-C motif chemokine ligand 8 Homo sapiens 329-342 17917246-7 2007 These results indicated that IL-8 mRNA expression was upregulated by NFkappaB and AP-1 in U937 cells stimulated with Glc-HSA and GA-HSA, but the signaling pathways were different. glc-hsa 117-124 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 17917246-7 2007 These results indicated that IL-8 mRNA expression was upregulated by NFkappaB and AP-1 in U937 cells stimulated with Glc-HSA and GA-HSA, but the signaling pathways were different. ga-hsa 129-135 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 17760719-11 2007 We confirmed that capsaicin inhibited IL-8 mRNA expression after infection of gastric epithelial cells with H. pylori for 6 hours. Capsaicin 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 17711487-2 2007 To investigate this, we studied the effect of two glucocorticoids (dexamethasone and triamcinolone acetonide) on reducing lipopolysaccharide (LPS)- and tumour necrosis factor (TNF)-alpha-induced interleukin (IL)-8 release in a monocytic cell line and two lymphocytic cell lines (HUT-78 and Jurkat). Triamcinolone Acetonide 85-108 C-X-C motif chemokine ligand 8 Homo sapiens 195-213 17711487-3 2007 The effect of the histone deacetylase inhibitor trichostatin A (TSA) on LPS- and TNF-alpha-induced IL-8 release and its repression by glucocorticoids was also examined. trichostatin A 48-62 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 17711487-3 2007 The effect of the histone deacetylase inhibitor trichostatin A (TSA) on LPS- and TNF-alpha-induced IL-8 release and its repression by glucocorticoids was also examined. trichostatin A 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 17711487-4 2007 LPS and TNF-alpha induced IL-8 release in all three cell lines and this induction was inhibited by both dexamethasone and triamcinolone. Dexamethasone 104-117 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 17711487-4 2007 LPS and TNF-alpha induced IL-8 release in all three cell lines and this induction was inhibited by both dexamethasone and triamcinolone. Triamcinolone 122-135 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 17711487-5 2007 Pretreatment of cells with TSA enhanced basal and LPS- and TNFalpha-stimulated IL-8 release in all three cell lines. trichostatin A 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 17711487-6 2007 TSA also attenuated the inhibitory effect of glucocorticoids on stimulated IL-8 release. trichostatin A 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 17711487-7 2007 Chromatin immunoprecipitation assays confirmed that LPS and TNF-alpha enhanced histone acetylation at the IL-8 promoter and that this was inhibited by triamcinolone in all three cell types. Triamcinolone 151-164 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 17662277-7 2007 Lower levels of IL-10 and IL-8 were found in quiet stage uveitis (surgical) samples compared with active uveitis (diagnostic) samples and in samples of patients treated with methotrexate (MTX) compared with samples of patients not treated with MTX. Methotrexate 174-186 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 17662277-7 2007 Lower levels of IL-10 and IL-8 were found in quiet stage uveitis (surgical) samples compared with active uveitis (diagnostic) samples and in samples of patients treated with methotrexate (MTX) compared with samples of patients not treated with MTX. Methotrexate 188-191 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 17513150-6 2007 Although IGF-I stimulated the phosphorylation of both Akt (protein kinase B) and extracellular-regulated kinase (ERK), the effect of IGF-I at IL-8 expression was inhibited only by U0126, a pharmacological inhibitor of MAPK/ERK kinase (MEK) and not by inhibition of the upstream activator of Akt, phosphatidylinositol-3 kinase (PI3K). U 0126 180-185 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 17680813-5 2007 Co-incubation of SCD neutrophils with KT5720 (an inhibitor of PKA) abrogated increased basal SCD neutrophil adhesion, spontaneous chemotaxis and IL-8-stimulated chemotaxis. KT 5720 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 17680813-6 2007 Stimulation of SCD neutrophils with IL-8 also significantly augmented SCD neutrophil adhesion to FN with a concomitant increase in cAMP levels and this increase in adhesion was abolished by KT5720. Cyclic AMP 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 17760719-3 2007 Herein, we demonstrated that capsaicin inhibited the release of pro-inflammatory cytokine, interleukin-8 (IL-8) by H. pylori-infected gastric epithelial cells through nuclear factor-kappaB (NF-kappaB) signal pathway. Capsaicin 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 17760719-6 2007 We measured IL-8 mRNA transcripts in H. pylori-infected gastric epithelial cells co-treated with capsaicin by reverse transcriptase-polymerase chain reaction analysis. Capsaicin 97-106 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 17760719-9 2007 RESULTS: Capsaicin inhibits H. pylori-induced IL-8 production by gastric epithelial cells in dose- and time-dependent manner. Capsaicin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 17760719-10 2007 Capsaicin as low as 100 micromol/L significantly inhibited IL-8 production in H. pylori-infected MKN45 cells (43.2% of control) at 24 hours incubation, whereas inhibited IL-8 production in H. pylori-infected AGS cells (70% of control). Capsaicin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 17760719-10 2007 Capsaicin as low as 100 micromol/L significantly inhibited IL-8 production in H. pylori-infected MKN45 cells (43.2% of control) at 24 hours incubation, whereas inhibited IL-8 production in H. pylori-infected AGS cells (70% of control). Capsaicin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 17760719-14 2007 CONCLUSIONS: Nontoxic dose of capsaicin inhibited H. pylori-induced IL-8 production by gastric epithelial cells through the modulation of IkappaB-, NF-kappaB-, and IL-8 pathways. Capsaicin 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 17760719-14 2007 CONCLUSIONS: Nontoxic dose of capsaicin inhibited H. pylori-induced IL-8 production by gastric epithelial cells through the modulation of IkappaB-, NF-kappaB-, and IL-8 pathways. Capsaicin 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 17760719-15 2007 We conclude that capsaicin can be proposed as a potential anti-inflammatory drug by inhibition of the production of IL-8 in H. pylori-infected gastric epithelium. Capsaicin 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 18026701-7 2007 RESULTS: Glucosamine significantly suppressed the IL-1beta-induced IL-8 production as well as its mRNA expression (p < 0.05) at 1 mM. Glucosamine 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 18026701-10 2007 CONCLUSIONS: These observations suggest that glucosamine can suppress the IL-1beta-mediated activation of synoviocytes (such as IL-8-, nitric oxide- and PGE(2)-production, and phosphorylation of p38 MAPK), thereby possibly exhibiting antiinflammatory actions in arthritis. Glucosamine 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17532154-4 2007 Marinosomes contributed to reduce inflammation induced by croton oil by regulating PGE2 and IL-8 production in human keratinocyte cultures. marinosomes 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 17920466-4 2007 Phagocytosis of the polyethylene particles or retrieved polyethylene particles by differentiated U937 cells stimulated the release of cytokines including interleukin 1beta, interleukin 6, interleukin 8, and vascular endothelial growth factor. Polyethylene 20-32 C-X-C motif chemokine ligand 8 Homo sapiens 188-201 17786306-12 2007 Cepharanthin inhibited the production of IR-induced IL-6 and IL-8, which are downstream targets of NF-kappaB. cepharanthine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 17920466-4 2007 Phagocytosis of the polyethylene particles or retrieved polyethylene particles by differentiated U937 cells stimulated the release of cytokines including interleukin 1beta, interleukin 6, interleukin 8, and vascular endothelial growth factor. Polyethylene 56-68 C-X-C motif chemokine ligand 8 Homo sapiens 188-201 17920466-5 2007 Microarray analysis revealed that the expression of IL8, CCL4, CXCR4, and some other genes was up-regulated after contact with retrieved polyethylene particles. Polyethylene 137-149 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 17932597-4 2007 METHODS: The effects of the LABAs salmeterol and formoterol on the synthesis of soluble interleukin-8 (IL-8), granulocyte-macrophage colony-stimulating factor (GM-CSF), and vascular endothelial growth factor (VEGF) in the human airway epithelial cell line A549 was investigated in vitro. Salmeterol Xinafoate 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 17932597-4 2007 METHODS: The effects of the LABAs salmeterol and formoterol on the synthesis of soluble interleukin-8 (IL-8), granulocyte-macrophage colony-stimulating factor (GM-CSF), and vascular endothelial growth factor (VEGF) in the human airway epithelial cell line A549 was investigated in vitro. Formoterol Fumarate 49-59 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 17932597-6 2007 RESULTS: Both salmeterol and formoterol significantly suppressed IL-8, GM-CSF, and VEGF secretion from tumor necrosis factor-alpha-stimulated A549 cells. Salmeterol Xinafoate 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 17932597-6 2007 RESULTS: Both salmeterol and formoterol significantly suppressed IL-8, GM-CSF, and VEGF secretion from tumor necrosis factor-alpha-stimulated A549 cells. Formoterol Fumarate 29-39 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 17932597-7 2007 Results indicated that formoterol was more potent than salmeterol in suppressing IL-8 and VEGF production. Formoterol Fumarate 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 17932597-7 2007 Results indicated that formoterol was more potent than salmeterol in suppressing IL-8 and VEGF production. Salmeterol Xinafoate 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 17884996-6 2007 Finally, IL-8 production of LPS-stimulated human pulmonary epithelial cells could be significantly reduced by these flavonoids. Flavonoids 116-126 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 18090004-3 2007 To elucidate the mechanisms underlying the immunosuppressive effects of ethanol, we investigated whether ethanol pretreatment may influence the changes in adhesion molecule expression induced by lipopolysaccharide (LPS) or interleukin (IL)-8 in human whole blood. Ethanol 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 223-241 18090004-10 2007 Stimulation with IL-8 significantly upregulated CD11b expression (5.3 +/- 1.7 to 7.5 +/- 2.7, p < 0.01) and this IL-8-induced upregulation of CD11b was also inhibited by ethanol pretreatment (p < 0.001). Ethanol 173-180 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 18090004-10 2007 Stimulation with IL-8 significantly upregulated CD11b expression (5.3 +/- 1.7 to 7.5 +/- 2.7, p < 0.01) and this IL-8-induced upregulation of CD11b was also inhibited by ethanol pretreatment (p < 0.001). Ethanol 173-180 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 17667842-3 2007 We studied the effect of azithromycin (AZM) on the suppression of NF-kappaB activation and the synthesis of pro-inflammatory cytokines IL-6 and IL-8 by TA cells obtained from premature infants. Azithromycin 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 17700564-7 2007 Moreover, IL-33-mediated IL-8 production by HUCBMCs was markedly reduced by the p38 MAPK inhibitor, SB203580. hucbmcs 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 17700564-7 2007 Moreover, IL-33-mediated IL-8 production by HUCBMCs was markedly reduced by the p38 MAPK inhibitor, SB203580. SB 203580 100-108 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 17667842-3 2007 We studied the effect of azithromycin (AZM) on the suppression of NF-kappaB activation and the synthesis of pro-inflammatory cytokines IL-6 and IL-8 by TA cells obtained from premature infants. Azithromycin 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 17667842-8 2007 AZM significantly reduced the IL-6 and IL-8 production to the levels similar to control. Azithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 18050667-3 2007 Tubes containing NaF in addition to EDTA, usually used for measurement of plasma glucose and HbA1c in diabetic patients, could be used for the collection of plasma sample. Glucose 81-88 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 17636245-0 2007 Transcriptional regulation of deoxynivalenol-induced IL-8 expression in human monocytes. deoxynivalenol 30-44 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 17636245-7 2007 Consistent with reporter studies, the NF-kappaB inhibitor caffeic acid phenethyl ester completely ablated both DON-induced IL-8 mRNA and protein expression. caffeic acid phenethyl ester 58-86 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 17636245-7 2007 Consistent with reporter studies, the NF-kappaB inhibitor caffeic acid phenethyl ester completely ablated both DON-induced IL-8 mRNA and protein expression. deoxynivalenol 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 17636245-10 2007 Taken together, these data suggest that DON-induced IL-8 expression is likely to be mediated at the transcriptional level by NF-kappaB, specifically p65, but does not appear to involve mRNA stabilization. deoxynivalenol 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 17636246-3 2007 In this work, we showed that NiSO(4) induced the expression of HLA-DR, CD83, CD86, and CD40 and the production of interleukin (IL)-8, IL-6, and IL-12p40 in human DCs, whereas DNCB induced mainly the expression of CD83 and CD86 and the production of IL-8. niso 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 249-253 17631879-0 2007 Combination of fluticasone propionate and salmeterol potentiates the suppression of cigarette smoke-induced IL-8 production by macrophages. Fluticasone 15-37 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 17631879-0 2007 Combination of fluticasone propionate and salmeterol potentiates the suppression of cigarette smoke-induced IL-8 production by macrophages. Salmeterol Xinafoate 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 17631879-4 2007 The aim of this study was to determine whether combined fluticasone propionate, a corticosteroid, and salmeterol, a long-acting beta(2)-adrenoceptor agonist, can suppress IL-8 production by human macrophages. Fluticasone 56-78 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 17631879-4 2007 The aim of this study was to determine whether combined fluticasone propionate, a corticosteroid, and salmeterol, a long-acting beta(2)-adrenoceptor agonist, can suppress IL-8 production by human macrophages. Salmeterol Xinafoate 102-112 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 17407152-5 2007 After 24 h, the early effect of TCDD on adipocytes was predominantly on inflammation, particularly induction of COX-2 and KC (IL-8), which is accompanied by upregulation of C/EBPbeta and delta. Polychlorinated Dibenzodioxins 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 17631879-7 2007 IL-8 release by cigarette smoke was significantly suppressed in a concentration-dependent manner by fluticasone and salmeterol. Fluticasone 100-111 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 17631879-7 2007 IL-8 release by cigarette smoke was significantly suppressed in a concentration-dependent manner by fluticasone and salmeterol. Salmeterol Xinafoate 116-126 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 17631879-9 2007 Interestingly, preincubation of cells with suboptimal concentration of salmeterol for 4 h before fluticasone administration for 30 min potentiates the inhibitory effect of fluticasone on IL-8 release. Salmeterol Xinafoate 71-81 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 17631879-9 2007 Interestingly, preincubation of cells with suboptimal concentration of salmeterol for 4 h before fluticasone administration for 30 min potentiates the inhibitory effect of fluticasone on IL-8 release. Fluticasone 172-183 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 17785828-2 2007 After priming with IFN-gamma and stimulation with NadADelta351-405, mo-DCs strongly up-regulated maturation markers CD83, CD86, CD80, and HLA-DR, secreted moderate quantities of TNF-alpha, IL-6, and IL-8, and produced a slight, although significant, amount of IL-12p70. nadadelta351 50-62 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 17513351-1 2007 The importance of intramolecular disulfides in a noncovalent dimeric protein interleukin-8 (IL-8) has been studied by replacing cysteines in each of the two disulfide pairs with alpha-aminobutyric acid (CH(2)-SH --> CH(2)-CH(3)). Disulfides 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 17513351-1 2007 The importance of intramolecular disulfides in a noncovalent dimeric protein interleukin-8 (IL-8) has been studied by replacing cysteines in each of the two disulfide pairs with alpha-aminobutyric acid (CH(2)-SH --> CH(2)-CH(3)). Disulfides 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 17513351-1 2007 The importance of intramolecular disulfides in a noncovalent dimeric protein interleukin-8 (IL-8) has been studied by replacing cysteines in each of the two disulfide pairs with alpha-aminobutyric acid (CH(2)-SH --> CH(2)-CH(3)). Cysteine 128-137 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 17513351-1 2007 The importance of intramolecular disulfides in a noncovalent dimeric protein interleukin-8 (IL-8) has been studied by replacing cysteines in each of the two disulfide pairs with alpha-aminobutyric acid (CH(2)-SH --> CH(2)-CH(3)). Cysteine 128-137 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 17513351-1 2007 The importance of intramolecular disulfides in a noncovalent dimeric protein interleukin-8 (IL-8) has been studied by replacing cysteines in each of the two disulfide pairs with alpha-aminobutyric acid (CH(2)-SH --> CH(2)-CH(3)). Disulfides 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 17513351-1 2007 The importance of intramolecular disulfides in a noncovalent dimeric protein interleukin-8 (IL-8) has been studied by replacing cysteines in each of the two disulfide pairs with alpha-aminobutyric acid (CH(2)-SH --> CH(2)-CH(3)). Disulfides 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 17513351-6 2007 Deleting either disulfide in IL-8 results in substantial loss in receptor activity, indicating that both disulfides are critical for function in the folded protein. Disulfides 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 17513351-6 2007 Deleting either disulfide in IL-8 results in substantial loss in receptor activity, indicating that both disulfides are critical for function in the folded protein. Disulfides 105-115 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 17678632-5 2007 Pretreatment of human intestinal epithelial HT-29 cells with TMMC also significantly inhibited the IL-8 and extracellular matrix metalloproteinase-7 levels induced by TNF-alpha. 2',4',6'-tris(methoxymethoxy) chalcone 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 99-148 18078616-1 2007 OBJECTIVES: Recent studies demonstrated in vivo the effectiveness of statins in reducing the inflammatory response in rheumatic diseases, and still more recently, simvastatin has been reported to inhibit in vitro IL-6 and IL-8 production by unstimulated fibroblast-like-synoviocytes (FLS) from rheumatoid arthritis (RA) patients. Simvastatin 163-174 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 17850672-0 2007 Differential regulation of iron chelator-induced IL-8 synthesis via MAP kinase and NF-kappaB in immortalized and malignant oral keratinocytes. Iron 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 17850672-2 2007 In the present study, we examined the expression and mechanism of IL-8 in which it is involved by treating immortalized (IHOK) and malignant human oral keratinocytes (HN12) cells with deferoxamine (DFO). Deferoxamine 184-196 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17850672-2 2007 In the present study, we examined the expression and mechanism of IL-8 in which it is involved by treating immortalized (IHOK) and malignant human oral keratinocytes (HN12) cells with deferoxamine (DFO). Deferoxamine 198-201 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17850672-6 2007 RESULTS: IHOK cells incubated with DFO showed increased expression of IL-8 mRNA, as well as higher release of the IL-8 protein. Deferoxamine 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17850672-6 2007 RESULTS: IHOK cells incubated with DFO showed increased expression of IL-8 mRNA, as well as higher release of the IL-8 protein. Deferoxamine 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 17850672-7 2007 The up-regulation of DFO-induced IL-8 expression was higher in IHOK cells than in HN12 cells and was concentration-dependent. Deferoxamine 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17850672-8 2007 DFO acted additively with IL-1beta to strongly up-regulate IL-8 in IHOK cells but not in HN12 cells. Deferoxamine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 17850672-9 2007 Accordingly, selective p38 and ERK1/2 inhibitors for both kinases abolished DFO-induced IL-8 expression in both IHOK and HN12 cells. Deferoxamine 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 17850672-11 2007 The IL-8 inducing effects of DFO were mediated by a nitric oxide donor (S-nitrosoglutathione), and by pyrrolidine dithiocarbamate, an inhibitor of NF-kappaB, as well as by wortmannin, which inhibits the phosphatidylinositol 3-kinase-dependent activation of NAD(P)H oxidase. Deferoxamine 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 17850672-11 2007 The IL-8 inducing effects of DFO were mediated by a nitric oxide donor (S-nitrosoglutathione), and by pyrrolidine dithiocarbamate, an inhibitor of NF-kappaB, as well as by wortmannin, which inhibits the phosphatidylinositol 3-kinase-dependent activation of NAD(P)H oxidase. Nitric Oxide 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 17850672-11 2007 The IL-8 inducing effects of DFO were mediated by a nitric oxide donor (S-nitrosoglutathione), and by pyrrolidine dithiocarbamate, an inhibitor of NF-kappaB, as well as by wortmannin, which inhibits the phosphatidylinositol 3-kinase-dependent activation of NAD(P)H oxidase. S-Nitrosoglutathione 74-92 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 17850672-11 2007 The IL-8 inducing effects of DFO were mediated by a nitric oxide donor (S-nitrosoglutathione), and by pyrrolidine dithiocarbamate, an inhibitor of NF-kappaB, as well as by wortmannin, which inhibits the phosphatidylinositol 3-kinase-dependent activation of NAD(P)H oxidase. pyrrolidine dithiocarbamic acid 102-129 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 17850672-11 2007 The IL-8 inducing effects of DFO were mediated by a nitric oxide donor (S-nitrosoglutathione), and by pyrrolidine dithiocarbamate, an inhibitor of NF-kappaB, as well as by wortmannin, which inhibits the phosphatidylinositol 3-kinase-dependent activation of NAD(P)H oxidase. Wortmannin 172-182 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 17850672-12 2007 CONCLUSION: This results demonstrate that DFO-induced IL-8 acts via multiple signaling pathways in immortalized and malignant oral keratinocytes, and that the control of IL-8 may be an important target for immunotheraphy against human oral premalignant lesions. Deferoxamine 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 17850672-12 2007 CONCLUSION: This results demonstrate that DFO-induced IL-8 acts via multiple signaling pathways in immortalized and malignant oral keratinocytes, and that the control of IL-8 may be an important target for immunotheraphy against human oral premalignant lesions. Deferoxamine 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 18219763-6 2007 IL-17 binding to an IL-17 receptor expressed on epithelial, endothelial, and fibroblastic stromal cells triggers the activation of transcription factor NF-kappaB and mitogen-activated protein kinase (p-38), which in turn results in the secretion of IL-1, TNF-alpha, IL-6, IL-8, or prostaglandin E2. Dinoprostone 281-297 C-X-C motif chemokine ligand 8 Homo sapiens 272-276 18078616-7 2007 Simvastatin significantly inhibited (about 20%) IL-6 and IL-8 production from IL-1-stimulated FLS. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 18078616-10 2007 CONCLUSION: Simvastatin significantly inhibits the production of IL-6 and IL-8 also in IL-1-stimulated FLS, even though to a lesser extent than in unstimulated cells, via a HMG-CoA-reductase block with an interference in prenylation process and NF-kB activation. Simvastatin 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 17470570-4 2007 We hypothesized that exercise-induced nitric oxide (NO) production is an important signaling event for IL-6, IL-8, HO-1, and HSP72 expression in muscle. Nitric Oxide 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 17470570-7 2007 L-NAME caused marked reductions in exercise-induced expression of 4 of 11 mRNAs including IL-6, IL-8, and HO-1. NG-Nitroarginine Methyl Ester 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 17449633-7 2007 LPS and the proinflammatory cytokines TNF-alpha, IL1beta, IFN-gamma, and sodium butyrate stimulation increased IL31, IL31Ralpha, and OSMR mRNA expression, while IL31 itself enhanced IL8 expression in IEC. Butyric Acid 73-88 C-X-C motif chemokine ligand 8 Homo sapiens 182-185 17671691-6 2007 All examined pancreatic carcinoma cells expressed CXCL-8 and TNFRII mRNA constitutively in RPMI-1640 medium without FBS. rpmi-1640 medium 91-107 C-X-C motif chemokine ligand 8 Homo sapiens 50-56 17680645-0 2007 Palmitic acid induces production of proinflammatory cytokine interleukin-8 from hepatocytes. Palmitic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 17680645-8 2007 Importantly, palmitic acid was found to induce significantly elevated levels of biologically active neutrophil chemoattractant, IL-8, from steatotic hepatocytes. Palmitic Acid 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17680645-9 2007 Incubation of the cells with palmitate led to increased IL-8 gene expression and secretion (both mRNA and protein) through mechanisms involving activation of nuclear factor kappaB (NF-kappaB) and c-Jun N-terminal kinase/activator protein-1. Palmitates 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 17671691-8 2007 Actinomycin D suppressed and cycloheximide augmented CXCL-8 mRNA which was induced by TNF-alpha or not. Cycloheximide 29-42 C-X-C motif chemokine ligand 8 Homo sapiens 53-59 17629956-6 2007 And, inhibitors of NF-kappaB (caffeic acid phenylethyl ester), p38 (SB 203580), or ERK1/2 (PD 98059) significantly reduced IL-8 induction by the organism. caffeic acid phenethyl ester 30-60 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 17495961-6 2007 Furthermore, incubation with DMF before stimulation with IL-1beta resulted in a significant decrease in NF-kappaB binding to the IL-8 kappaB and the IL-20 kappaB-binding sites as well as a subsequent decrease in IL-8 and IL-20 mRNA expression. Dimethyl Fumarate 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 17628646-8 2007 Dexamethasone treatment of BECs only partially suppressed IP-10 and TNF-alpha but was more effective at suppressing RANTES, IL-6, and IL-8. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 18193101-10 2007 Treatment with a proton pump inhibitor, lansoprazole reduces the mucosal levels of IL-8 mRNA and protein in GERD, including RE and NERD. Lansoprazole 40-52 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 17876544-10 2007 Inhibitors for ERK (PD98059 and U0216) and p38 MAPK (SB203580) significantly reduced the IL-17F-induced IL-6, IL-8, LIF, MMP-1, and MMP-3 secretion. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 17876544-10 2007 Inhibitors for ERK (PD98059 and U0216) and p38 MAPK (SB203580) significantly reduced the IL-17F-induced IL-6, IL-8, LIF, MMP-1, and MMP-3 secretion. u0216 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 17876544-10 2007 Inhibitors for ERK (PD98059 and U0216) and p38 MAPK (SB203580) significantly reduced the IL-17F-induced IL-6, IL-8, LIF, MMP-1, and MMP-3 secretion. SB 203580 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 17495961-6 2007 Furthermore, incubation with DMF before stimulation with IL-1beta resulted in a significant decrease in NF-kappaB binding to the IL-8 kappaB and the IL-20 kappaB-binding sites as well as a subsequent decrease in IL-8 and IL-20 mRNA expression. Dimethyl Fumarate 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 17697714-1 2007 This study concerns effects on water-borne lead from combinations of chlorine (CL) or chloramines (CA) with fluosilicic acid (FSA) or sodium fluoride (NaF). Water 31-36 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 17216397-2 2007 The main objectives were: (1) to evaluate the effect of diode laser-NaF varnish combination on binding fluoride to dental enamel in an in vitro model and (2) to analyse outer enamel surface changes produced by the laser energy. Fluorides 103-111 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 17446059-6 2007 EGCG significantly inhibited the IL-1beta+Abeta (25-35)-induced IL-6, IL-8, vascular endothelial growth factor (VEGF) and prostaglandin (PG)E(2) production at 24 h (P<.01). epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17446059-6 2007 EGCG significantly inhibited the IL-1beta+Abeta (25-35)-induced IL-6, IL-8, vascular endothelial growth factor (VEGF) and prostaglandin (PG)E(2) production at 24 h (P<.01). UNII-042A8N37WH 42-47 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17446059-7 2007 The maximal inhibition rate of IL-6, IL-8, VEGF and PGE(2) production by EGCG was approximately 54.40%, 56.01%, 69.06% and 47.03%, respectively. epigallocatechin gallate 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 17876051-8 2007 Kaempferol suppressed the expression of proinflammatory cytokine interleukin-6 and chemokines interleukin-8, monocyte chemoattractant protein-1, and regulated on activation, normal T-cell expressed and secreted. kaempferol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 17519305-12 2007 Simvastatin therapy significantly inhibited lipopolysaccharide-activated monocyte release of O(2)(-) (P < 0.0005), IL-8 (P < 0.03), and TNF (P < 0.02). Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 17558435-0 2007 Virodhamine and CP55,940 modulate cAMP production and IL-8 release in human bronchial epithelial cells. virodhamine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 17558435-0 2007 Virodhamine and CP55,940 modulate cAMP production and IL-8 release in human bronchial epithelial cells. 1(4H)-Pyridinepropanoic acid, 3-hydroxy-2-methyl-4-oxo-, ethyl ester 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 17558435-13 2007 In the absence of agonist, SR144528 by itself reduced TNF-alpha induced IL-8 release. SR 144528 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 18048020-4 2007 CNTO2424 down-regulates poly(I:C)-induced production of IL-6, IL-8, MCP-1, RANTES, and IP-10 in human lung epithelial cells. poly 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 18048020-4 2007 CNTO2424 down-regulates poly(I:C)-induced production of IL-6, IL-8, MCP-1, RANTES, and IP-10 in human lung epithelial cells. Carbon 0-1 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 17604003-12 2007 The decrease of IL-8 secretion from IEC was more pronounced after pre-incubation with 13-Oxo-ODE compared to the PPARgamma agonist troglitazone and higher as with the known PPARgamma ligands 13-HODE and 15-HETE. 13-oxo-9,11-octadecadienoic acid 86-96 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 17604003-12 2007 The decrease of IL-8 secretion from IEC was more pronounced after pre-incubation with 13-Oxo-ODE compared to the PPARgamma agonist troglitazone and higher as with the known PPARgamma ligands 13-HODE and 15-HETE. Troglitazone 131-143 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 17604003-12 2007 The decrease of IL-8 secretion from IEC was more pronounced after pre-incubation with 13-Oxo-ODE compared to the PPARgamma agonist troglitazone and higher as with the known PPARgamma ligands 13-HODE and 15-HETE. 13-hydroxy-9,11-octadecadienoic acid 191-198 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 17604003-12 2007 The decrease of IL-8 secretion from IEC was more pronounced after pre-incubation with 13-Oxo-ODE compared to the PPARgamma agonist troglitazone and higher as with the known PPARgamma ligands 13-HODE and 15-HETE. 15-hydroxy-5,8,11,13-eicosatetraenoic acid 203-210 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 17667496-10 2007 Elevated plasma levels of IL-6, IL-8, complement C3a, and IL-1ra as well as expression of CD11b, L- and P-selectin, and platelet-leukocyte aggregates were significantly attenuated by systemic lidocaine. Lidocaine 192-201 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 17517880-11 2007 Interestingly, TcdB-treated HMC-1 cells, but not latrunculin B-treated HMC-1 cells, showed a strong p38 MAPK-dependent increase in interleukin-8 release. trimethylaminocarboxyldihydroboran 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 131-144 17504902-0 2007 Metformin suppresses interleukin (IL)-1beta-induced IL-8 production, aromatase activation, and proliferation of endometriotic stromal cells. Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 17504902-5 2007 RESULTS: Metformin dose-dependently suppressed IL-1beta-induced IL-8 production, cAMP-induced mRNA expression and aromatase activity, and 5-bromo-2"-deoxyuridine incorporation in ESCs. Metformin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 17442054-3 2007 Pre-treatment of immortalized HBMEC with atorvastatin (50 nmol/L to 1 micromol/L) dose-dependently prevented an inflammatory up-regulation of monocyte chemoattractant protein-1/CCL2 but not of interleukin-8/CXCL8 and intercellular adhesion molecule-1 expression by tumor necrosis factor-alpha or interleukin-1beta. Atorvastatin 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 193-206 17442054-3 2007 Pre-treatment of immortalized HBMEC with atorvastatin (50 nmol/L to 1 micromol/L) dose-dependently prevented an inflammatory up-regulation of monocyte chemoattractant protein-1/CCL2 but not of interleukin-8/CXCL8 and intercellular adhesion molecule-1 expression by tumor necrosis factor-alpha or interleukin-1beta. Atorvastatin 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 207-212 17496166-5 2007 Sch527123 inhibited neutrophil chemotaxis and myeloperoxidase release in response to CXCL1 and CXCL8 but had no effect on the response of these cells to C5a or formyl-methionyl-leucyl-phenylalanine. 2-hydroxy-N,N-dimethyl-3-(2-((1-(5-methylfuran-2-yl)propyl)amino)-3,4-dioxocyclobut-1-enylamino)benzamide 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 17433832-10 2007 LPS-stimulated IL-6, TNF-alpha, PGE(2) and PGF(2alpha) release was significantly suppressed by treatment with all concentrations of SB202190, whereas ILS-stimulated IL-1beta release was only significantly inhibited in the presence of 50 microM SB202190 and there was no effect of SB202190 on LPS-stimulated IL-8 release. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 132-140 C-X-C motif chemokine ligand 8 Homo sapiens 307-311 17488804-8 2007 The mechanism of caffeine seems to involve the inhibition of the extracellular signal-regulated kinase 1/2 (ERK1/2), p38, and Akt, leading to a marked decrease in adenosine-induced HIF-1alpha accumulation, VEGF transcriptional activation, and VEGF and IL-8 protein accumulation. Caffeine 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 17488804-8 2007 The mechanism of caffeine seems to involve the inhibition of the extracellular signal-regulated kinase 1/2 (ERK1/2), p38, and Akt, leading to a marked decrease in adenosine-induced HIF-1alpha accumulation, VEGF transcriptional activation, and VEGF and IL-8 protein accumulation. Adenosine 163-172 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 17488804-11 2007 These data provide evidence that adenosine could modulate the migration of colon cancer cells by an HIF-1alpha/VEGF/IL-8-dependent mechanism and that caffeine has the potential to inhibit colon cancer cell growth. Adenosine 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 17488804-0 2007 Caffeine inhibits adenosine-induced accumulation of hypoxia-inducible factor-1alpha, vascular endothelial growth factor, and interleukin-8 expression in hypoxic human colon cancer cells. Caffeine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 125-138 17488804-0 2007 Caffeine inhibits adenosine-induced accumulation of hypoxia-inducible factor-1alpha, vascular endothelial growth factor, and interleukin-8 expression in hypoxic human colon cancer cells. Adenosine 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 125-138 17488804-7 2007 Pretreatment of cells with caffeine significantly reduces adenosine-induced VEGF promoter activity and VEGF and IL-8 expression. Caffeine 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 17504764-4 2007 Mutagenesis and biochemical analyses revealed that (a) the integrity of the detergent-resistant membranes is necessary for dl-CD40 homodimer formation, (b) the cytoplasmic Cys(238) of CD40 is the target for the de novo disulfide oxidation induced by receptor oligomerization, and (c) dl-CD40 homodimer formation is required for CD40-induced interleukin-8 secretion. Cysteine 172-175 C-X-C motif chemokine ligand 8 Homo sapiens 341-354 17608466-0 2007 Synthesis and biological evaluation of N-pyrazolyl-N"-alkyl/benzyl/phenylureas: a new class of potent inhibitors of interleukin 8-induced neutrophil chemotaxis. -pyrazolyl 40-50 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 17608466-0 2007 Synthesis and biological evaluation of N-pyrazolyl-N"-alkyl/benzyl/phenylureas: a new class of potent inhibitors of interleukin 8-induced neutrophil chemotaxis. Nitrogen 51-53 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 17608466-2 2007 We report here the synthesis of a new N-(4-substituted)pyrazolyl-N"-alkyl/benzyl/phenylureas that are potent inhibitors of interleukin-8 (IL8)-induced neutrophil chemotaxis. n-(4-substituted)pyrazolyl 38-64 C-X-C motif chemokine ligand 8 Homo sapiens 123-136 17608466-2 2007 We report here the synthesis of a new N-(4-substituted)pyrazolyl-N"-alkyl/benzyl/phenylureas that are potent inhibitors of interleukin-8 (IL8)-induced neutrophil chemotaxis. n-(4-substituted)pyrazolyl 38-64 C-X-C motif chemokine ligand 8 Homo sapiens 138-141 17608466-3 2007 The first series of compounds, obtained by functionalization with a urea moiety of the 5-amino-1-(2-hydroxy-2-phenylethyl)-1H-pyrazole-4-carboxylic acid ethyl ester 3, blocked the IL8-induced neutrophil chemotaxis, while they did not block N-formylmethionylleucylphenylalanine-mediated chemotaxis. Urea 68-72 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 17608466-3 2007 The first series of compounds, obtained by functionalization with a urea moiety of the 5-amino-1-(2-hydroxy-2-phenylethyl)-1H-pyrazole-4-carboxylic acid ethyl ester 3, blocked the IL8-induced neutrophil chemotaxis, while they did not block N-formylmethionylleucylphenylalanine-mediated chemotaxis. 5-amino-1-(2-hydroxy-2-phenylethyl)-1h-pyrazole-4-carboxylic acid ethyl ester 87-164 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 17638896-8 2007 IL8-S cells expressed 2- to 3-fold higher levels of phospho-EGFR, src, Akt, and nuclear factor kappaB (NF-kappaB) and showed increased survival when treated with docetaxel. Docetaxel 162-171 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 17599375-0 2007 Endocytosis, oxidative stress and IL-8 expression in human lung epithelial cells upon treatment with fine and ultrafine TiO2: role of the specific surface area and of surface methylation of the particles. titanium dioxide 120-124 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 17491020-2 2007 The alpha,beta-unsaturated aldehydes in cigarette smoke (acrolein and crotonaldehyde) inhibited production of interleukin-2 (IL-2), IL-10, granulocyte-macrophage colony-stimulating factor, interferon-gamma, and tumor necrosis factor-alpha by human T cells but did not inhibit production of IL-8. 2-butenal 70-84 C-X-C motif chemokine ligand 8 Homo sapiens 290-294 26110364-8 2007 Fibroblasts are also stimulated by DDHAM to secrete key proinflammatory(IL-1 and IL-6) and chemotactic cytokines or chemokines (proand IL-8) involved in regulating and enhancing wound repair processes. ddham 35-40 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 17491020-2 2007 The alpha,beta-unsaturated aldehydes in cigarette smoke (acrolein and crotonaldehyde) inhibited production of interleukin-2 (IL-2), IL-10, granulocyte-macrophage colony-stimulating factor, interferon-gamma, and tumor necrosis factor-alpha by human T cells but did not inhibit production of IL-8. alpha,beta-unsaturated aldehydes 4-36 C-X-C motif chemokine ligand 8 Homo sapiens 290-294 17491020-2 2007 The alpha,beta-unsaturated aldehydes in cigarette smoke (acrolein and crotonaldehyde) inhibited production of interleukin-2 (IL-2), IL-10, granulocyte-macrophage colony-stimulating factor, interferon-gamma, and tumor necrosis factor-alpha by human T cells but did not inhibit production of IL-8. Acrolein 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 290-294 17592301-12 2007 The PRBC group had a significantly different expression profile compared with the others and included up-regulation of the interleukin-8, toll-like receptor 4, cryropyrin, prostaglandin-endoperoxide synthase-2, and heparinase genes. prbc 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 123-158 17584482-9 2007 This study showed that application of ZBUF is more effective to decrease the level of inflammatory mediators including TNF-alpha, IL-6, and IL-8 than administration of MP after pediatric CPB. zbuf 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 17560458-11 2007 Culture supernatants from MCs and PMNs of TB patients contained increased amounts of IL-8 and TNFalpha. mcs 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17588396-8 2007 Methylprednisolone attenuated postoperative tumor necrosis factor-alpha, interleukin 6, interleukin 8, and C-reactive protein levels while increasing interleukin 10 release. Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 17581316-0 2007 Induction of urokinase-type plasminogen activator, interleukin-8 and early growth response-1 by STI571 through activating mitogen activated protein kinase in human small cell lung cancer cells. Imatinib Mesylate 96-102 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 17466485-0 2007 Simvastatin and fluvastatin reduce interleukin-6 and interleukin-8 lipopolysaccharide (LPS) stimulated production by isolated human monocytes from chronic kidney disease patients. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 53-66 17466485-0 2007 Simvastatin and fluvastatin reduce interleukin-6 and interleukin-8 lipopolysaccharide (LPS) stimulated production by isolated human monocytes from chronic kidney disease patients. Fluvastatin 16-27 C-X-C motif chemokine ligand 8 Homo sapiens 53-66 17581316-1 2007 We previously demonstrated the simultaneous induction of urokinase-type plasminogen activator and interleukin-8, a CXC chemokine, in doxorubicin-treated human NCI-H69 small cell lung cancer cells in which extracellular signal-regulated kinase 1/2 and p38 mitogen-activated protein kinase might be involved. Doxorubicin 133-144 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 17581316-3 2007 We therefore investigated the effects of STI571 on the expression of urokinase-type plasminogen activator and interleukin-8 in NCI-H69 cells. Imatinib Mesylate 41-47 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 17581316-6 2007 U0126, an inhibitor against extracellular signal-regulated kinase 1/2, however, only inhibited the STI571-induced interleukin-8 accumulation. U 0126 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 114-127 17581316-6 2007 U0126, an inhibitor against extracellular signal-regulated kinase 1/2, however, only inhibited the STI571-induced interleukin-8 accumulation. Imatinib Mesylate 99-105 C-X-C motif chemokine ligand 8 Homo sapiens 114-127 17317104-2 2007 Previously we found that TNF-alpha-induced reactive oxygen species (ROS) production is required for NF-kappaB action because antioxidants inhibited TNF-alpha-inducible IL-8 expression without affecting its nuclear translocation. Reactive Oxygen Species 43-66 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 17317104-2 2007 Previously we found that TNF-alpha-induced reactive oxygen species (ROS) production is required for NF-kappaB action because antioxidants inhibited TNF-alpha-inducible IL-8 expression without affecting its nuclear translocation. Reactive Oxygen Species 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 17317104-12 2007 These results indicate that the ROS-mediated TNF-alpha-induced IL-8 transcription is regulated by NF-kappaB/RelA phosphorylation at the critical Ser(276) residue by PKAc, resulting in stable enhanceosome formation on target genes. Reactive Oxygen Species 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 17550933-8 2007 CONCLUSIONS: Rapid withdrawal of inhaled corticosteroids results in an exacerbation of asthma that is preceded by an increase in sputum neutrophils and IL-8 concentrations, in contrast to an increase in eosinophils reported in previous studies in which inhaled steroids are slowly tapered. Steroids 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 17317104-12 2007 These results indicate that the ROS-mediated TNF-alpha-induced IL-8 transcription is regulated by NF-kappaB/RelA phosphorylation at the critical Ser(276) residue by PKAc, resulting in stable enhanceosome formation on target genes. Serine 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 17112620-8 2007 1,25-Dihydroxyvitamin D(3) was able to down-regulate the expression of TNF-alpha, IL-6, IL-1, and IL-8, confirming its immunomodulatory properties. Calcitriol 0-26 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 17403059-6 2007 Inhibition by TGF-beta1 was negated by SB-431542, a small molecule inhibitor that specifically blocks the kinase activity of the type I TGF-beta receptor (ALK5) In contrast to lactoferrin release, another important neutrophil function, interleukin (IL)-8 driven chemotaxis, was not affected by TGF-beta1 at 1 pg/ml or 100 pg/ml. 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 236-254 17888208-2 2007 In this study we evaluate whether simvastatin could influence the production of pro-inflammatory cytokines (interleukin (IL)-6 and IL-8) and nitric oxide (NO) by activated human chondrocytes. Simvastatin 34-45 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 17888208-5 2007 RESULTS: Simvastatin demonstrated significant dose-dependent inhibition of IL-6 and IL-8 production of isolated chondrocytes and cartilage explants up to 99% for IL-6 and up to 88% for IL-8 (p < 0.01). Simvastatin 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 17888208-5 2007 RESULTS: Simvastatin demonstrated significant dose-dependent inhibition of IL-6 and IL-8 production of isolated chondrocytes and cartilage explants up to 99% for IL-6 and up to 88% for IL-8 (p < 0.01). Simvastatin 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 17666914-6 2007 The expression of intracellular cell adhesion molecule (ICAM)-1, monocyte chemoattractant protein (MCP)-1, and interleukin (IL)-8 were attenuated by curcumin at both mRNA and protein level. Curcumin 149-157 C-X-C motif chemokine ligand 8 Homo sapiens 111-129 17609508-4 2007 In addition, PVAE attenuated phorbol 12-myristate 13-acetate (PMA) and calcium ionophore A23187-stimulated TNF-alpha, IL-6, and IL-8 secretion in human mast cells. pvae 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17609508-4 2007 In addition, PVAE attenuated phorbol 12-myristate 13-acetate (PMA) and calcium ionophore A23187-stimulated TNF-alpha, IL-6, and IL-8 secretion in human mast cells. Calcium 71-78 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17609508-4 2007 In addition, PVAE attenuated phorbol 12-myristate 13-acetate (PMA) and calcium ionophore A23187-stimulated TNF-alpha, IL-6, and IL-8 secretion in human mast cells. Calcimycin 89-95 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17880760-7 2007 IL-8 EBC levels decreased after antibiotic treatment (T0 0.36+/-0.03pg/ml vs T1 0.28+/-0.03pg/ml; p=0.03) and pH values increased (T0 7.36+/-0.09 vs T1 7.61+/-0.08; p=0.04). NSC638702 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 18409814-5 2007 Nickel contact at very low concentrations (10(-5), 10(-6) M) induced upregulation of MMP-2 and IL-8 mRNA production; chromium contact at very low concentrations killed all cells. Nickel 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 18409824-2 2007 We assessed urinary excretion of 1-naphthol (1-NAF), biomarker of naphthalene exposure, in non-occupationally exposed subjects. 1-naphthol 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 18409824-5 2007 Median concentration of 1-NAF was 6-fold higher in smokers compared to nonsmokers (respectively, 7.7 microg/g creatinine vs 1.3 microg/g creatinine). Creatinine 110-120 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 18409824-5 2007 Median concentration of 1-NAF was 6-fold higher in smokers compared to nonsmokers (respectively, 7.7 microg/g creatinine vs 1.3 microg/g creatinine). Creatinine 137-147 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 17880760-1 2007 Interleukin (IL)-8 is a major factor in inflammatory response and the IL-8 levels in exhaled breath condensate (EBC) may be used as a marker of airway inflammation. NSC638702 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17596547-3 2007 One of these involves addition of glycolysis inhibitors, such as sodium fluoride-potassium oxalate (NaF-KOx) to sample collection tubes, whereas the other requires immediate refrigeration and sample separation. sodium fluoride potassium oxalate 65-98 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 17579020-4 2007 The rODNs promoted the survival of macrophages and were able to activate IL-8 secretion through a chloroquine-resistant pathway. Chloroquine 98-109 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 17040605-8 2007 Our results showed that IL-5, IL-6 and IL-8 in both the AR and NAR groups were strikingly elevated in comparison with the control group (all p < 0.01 for AR group; p < 0.05, 0.05, 0.01, respectively, for NAR group); and they were even higher in the AR group than those in the NAR group (p < 0.01, 0.05, 0.01, respectively). Argon 56-58 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 17040605-8 2007 Our results showed that IL-5, IL-6 and IL-8 in both the AR and NAR groups were strikingly elevated in comparison with the control group (all p < 0.01 for AR group; p < 0.05, 0.05, 0.01, respectively, for NAR group); and they were even higher in the AR group than those in the NAR group (p < 0.01, 0.05, 0.01, respectively). Argon 64-66 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 17544805-3 2007 In this study we confirmed that NO regulates cytokine and chemokine release by resting MDM: accumulation of TNF-alpha, IL-12, IL-10, CCL5 (RANTES) and CXCL8 (IL-8) in MDM supernatants was significantly modified by the NO-donor S-nitroso-N-penicillamine (SNAP). s-nitroso-n-penicillamine 227-252 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 18958735-0 2007 Palladium attenuates the pro-inflammatory interactions of C5a, interleukin-8 and pneumolysin with human neutrophils. Palladium 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 17552048-4 2007 RESULTS: Infliximab plus MTX treatment resulted in more rapid decreases in levels of matrix metalloproteinase-3 (MMP-3), intercellular cell adhesion molecule-1, interleukin 8 (IL-8), and tumor necrosis factor-a than treatment with MTX alone. Methotrexate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 17552048-4 2007 RESULTS: Infliximab plus MTX treatment resulted in more rapid decreases in levels of matrix metalloproteinase-3 (MMP-3), intercellular cell adhesion molecule-1, interleukin 8 (IL-8), and tumor necrosis factor-a than treatment with MTX alone. Methotrexate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 17552048-6 2007 An increase in IL-8 levels from baseline to Week 54 correlated with worsening in vdHSS at Week 54 in the MTX-alone group. Methotrexate 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 17552048-9 2007 MMP-3 levels at different timepoints were consistently associated with clinical improvements at Week 54 in the infliximab plus MTX group, while increases in IL-8 levels correlated with a worsening in vdHSS at Week 54 in the MTX-alone group. Methotrexate 224-227 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 17606477-3 2007 Administration of recombinant human IL-8 induced a rapid, time-dependent increase in cyclin D1 expression in AIPC cells, a response attenuated by the translation inhibitor cycloheximide but not by the RNA synthesis inhibitor, actinomycin D. Cycloheximide 172-185 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 17606477-6 2007 LY294002 and rapamycin each abrogated the IL-8-promoted phosphorylation of rS6 and attenuated the rate of AIPC cell proliferation. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 17544805-3 2007 In this study we confirmed that NO regulates cytokine and chemokine release by resting MDM: accumulation of TNF-alpha, IL-12, IL-10, CCL5 (RANTES) and CXCL8 (IL-8) in MDM supernatants was significantly modified by the NO-donor S-nitroso-N-penicillamine (SNAP). snap 254-258 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 17606477-7 2007 Our results indicate that IL-8 signaling (a) regulates cyclin D1 expression at the level of translation, (b) regulates the activation of proteins associated with the translation of capped and 5"-oligopyrimidine tract transcripts, and (c) activates signal transduction pathways underpinning AIPC cell proliferation. oligopyrimidine 195-210 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 17290398-9 2007 Subcutaneous injection or oral administration of parthenolide showed significant tumor growth inhibition in the xenograft model via decreased production of interleukin-8 (IL-8) or vascular endothelial growth factor (VEGF). parthenolide 49-61 C-X-C motif chemokine ligand 8 Homo sapiens 156-169 17483743-5 2007 Among the PDF groups, IL-8 secretions from ECs and PMNs were lower with 100 and 1000 micromol/L Arg than with 0 and 50 micromol/L Arg, and this was consistent with the expression of the IL-8 receptor on PMNs. pdf 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 17483743-5 2007 Among the PDF groups, IL-8 secretions from ECs and PMNs were lower with 100 and 1000 micromol/L Arg than with 0 and 50 micromol/L Arg, and this was consistent with the expression of the IL-8 receptor on PMNs. pdf 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 17483743-5 2007 Among the PDF groups, IL-8 secretions from ECs and PMNs were lower with 100 and 1000 micromol/L Arg than with 0 and 50 micromol/L Arg, and this was consistent with the expression of the IL-8 receptor on PMNs. Arginine 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 17483743-5 2007 Among the PDF groups, IL-8 secretions from ECs and PMNs were lower with 100 and 1000 micromol/L Arg than with 0 and 50 micromol/L Arg, and this was consistent with the expression of the IL-8 receptor on PMNs. Arginine 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 17483743-5 2007 Among the PDF groups, IL-8 secretions from ECs and PMNs were lower with 100 and 1000 micromol/L Arg than with 0 and 50 micromol/L Arg, and this was consistent with the expression of the IL-8 receptor on PMNs. Arginine 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 17483743-8 2007 Inhibition of nitric oxide production results in high CAM and IL-8 expressions comparable with groups with low Arg administration. Nitric Oxide 14-26 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 17483743-11 2007 Arginine administration at levels similar to or higher than physiological concentrations reduced IL-8 and CAM expression, and PMN transmigration was also decreased after stimulation with plasma or PDF from surgical patients. Arginine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 17467667-4 2007 Palmitic acid (PA), the predominant saturated FFA released from adipose tissue, but not unsaturated FFA, induced an approximately 6-fold (p<0.05) increase in IP-10 gene expression (and 2- to 4-fold increases in IL-8, MCP-1, COX-2, and MIG). Palmitic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 17467667-4 2007 Palmitic acid (PA), the predominant saturated FFA released from adipose tissue, but not unsaturated FFA, induced an approximately 6-fold (p<0.05) increase in IP-10 gene expression (and 2- to 4-fold increases in IL-8, MCP-1, COX-2, and MIG). Palmitic Acid 15-17 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 17445776-7 2007 Furthermore, CCL-34 treatment stimulated NF-kappaB activation and IL-8 production in a 293 cell line constitutively expressing human TLR4, MD-2 and CD14. CCL 34 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17290398-9 2007 Subcutaneous injection or oral administration of parthenolide showed significant tumor growth inhibition in the xenograft model via decreased production of interleukin-8 (IL-8) or vascular endothelial growth factor (VEGF). parthenolide 49-61 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 17561043-2 2007 The purpose of this in-vitro study was to investigate the effect of sodium fluoride (Colgate Neutrafluor 9000 ppm) (NaF) and 10% casein phosphopeptide-amorphous calcium phosphate (GC Tooth Mousse) (TM) on enamel demineralization adjacent to orthodontic brackets. Sodium Fluoride 68-83 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 17512458-6 2007 Treatment of placenta and fetal membranes with 15-A(2)-IsoP caused a dose-dependent decrease in LPS-stimulated release of the cytokines IL-1beta, IL-6, IL-8, and TNF-alpha and the prostaglandins PGE(2) and PGF(2)alpha. 15-a(2)-isop 47-59 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 17141949-5 2007 Interestingly, imatinib mesylate (10 microM) strikingly induced the expression of the pro-inflammatory and pro-angiogenic cytokines interleukin (IL)-6 and IL-8, and mildly stimulated the release of vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF). Imatinib Mesylate 15-32 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 17369293-6 2007 Treatment of A549 cells with monocyte/PM(10) CM produced increased IL-8 release that was reduced with CM from monocyte/PM(10)/calcium antagonist treatments. Calcium 126-133 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 17322416-10 2007 We further confirmed that sirolimus inhibited mRNA and protein expression of inflammatory cytokines IL-6, tumor necrosis factor-alpha, IL-8, and monocyte chemoattractant protein-1. Sirolimus 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 17561043-12 2007 Application of TM/NaF with RMGIC significantly reduced DeltaF and %F compared with the control RMGIC (Tukey post-hoc test, P = .008, P = .019, respectively). Thulium 15-17 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 17561043-16 2007 The application of TM, NaF, or TM/NaF can significantly prevent enamel demineralization when CR is used for bonding. Chromium 93-95 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 17561043-16 2007 The application of TM, NaF, or TM/NaF can significantly prevent enamel demineralization when CR is used for bonding. Chromium 93-95 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 17389616-0 2007 Conjugated linoleic acids modulate UVR-induced IL-8 and PGE2 in human skin cells: potential of CLA isomers in nutritional photoprotection. Linoleic Acids 11-25 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 17418999-5 2007 Finally, an FPRL-1 receptor antagonist, boc-2 peptide reversed LXA(4) effect on IL-8 generation. N-(1H-benzimidazol-2-ylmethyl)-2-methoxyacetamide 63-66 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 17433258-8 2007 All peptides tested were effective at preventing IL-8 release from phorbol 12-myristate 13-acetate (PMA)/copper-stimulated human umbilical vein endothelial cells (HUVEC). Tetradecanoylphorbol Acetate 67-98 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 17433258-8 2007 All peptides tested were effective at preventing IL-8 release from phorbol 12-myristate 13-acetate (PMA)/copper-stimulated human umbilical vein endothelial cells (HUVEC). Tetradecanoylphorbol Acetate 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 17433258-8 2007 All peptides tested were effective at preventing IL-8 release from phorbol 12-myristate 13-acetate (PMA)/copper-stimulated human umbilical vein endothelial cells (HUVEC). Copper 105-111 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 17389616-8 2007 Additionally, t10,c12-CLA and tt-CLA inhibited TNF-alpha-induced IL-8 from 11 669 +/- 1692 pg/ng protein in control cells to 5540 +/- 191 (P < 0.001) and 8082 +/- 1298 pg/ng (P < 0.01) protein, respectively. c12-cla 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 17389616-8 2007 Additionally, t10,c12-CLA and tt-CLA inhibited TNF-alpha-induced IL-8 from 11 669 +/- 1692 pg/ng protein in control cells to 5540 +/- 191 (P < 0.001) and 8082 +/- 1298 pg/ng (P < 0.01) protein, respectively. tt-cla 30-36 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 17420239-4 2007 Addition of aferric, but not iron-saturated, enterobactin elicits a dose-dependent increase in secretion of the proinflammatory chemokine interleukin-8 by human respiratory epithelial cells in culture. Enterobactin 45-57 C-X-C motif chemokine ligand 8 Homo sapiens 138-151 17617053-7 2007 In other words, increased reactive oxygen species may induce interleukin-8 production and result in diminished reduced glutathione levels. Reactive Oxygen Species 26-49 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 17617741-4 2007 In these studies, the effect of 5alpha-dihydrotestosterone (DHT) on the expression levels of IL-6 and IL-8 was investigated. Dihydrotestosterone 32-58 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 17617741-4 2007 In these studies, the effect of 5alpha-dihydrotestosterone (DHT) on the expression levels of IL-6 and IL-8 was investigated. Dihydrotestosterone 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 17617741-8 2007 Furthermore, DHT enhanced IL-6 and IL-8 secretion. Dihydrotestosterone 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 17617741-9 2007 Flutamide (Flu), an AR antagonist, completely abolished DHT-stimulated cell growth and the expression of IL-6 and IL-8. Flutamide 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 17617741-9 2007 Flutamide (Flu), an AR antagonist, completely abolished DHT-stimulated cell growth and the expression of IL-6 and IL-8. Flutamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 17617741-9 2007 Flutamide (Flu), an AR antagonist, completely abolished DHT-stimulated cell growth and the expression of IL-6 and IL-8. Dihydrotestosterone 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 17538964-7 2007 In particular, the presence of intracellular NS5A led to increased transcriptional and protein expression of IL-8 (CXCL-8), a chemokine with proinflammatory and anti-interferon properties, and impaired interferon induction of signal transducers and activators of transcription 1 (STAT1) serine and tyrosine and STAT2 tyrosine phosphorylation. Serine 287-293 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 17538964-7 2007 In particular, the presence of intracellular NS5A led to increased transcriptional and protein expression of IL-8 (CXCL-8), a chemokine with proinflammatory and anti-interferon properties, and impaired interferon induction of signal transducers and activators of transcription 1 (STAT1) serine and tyrosine and STAT2 tyrosine phosphorylation. Tyrosine 298-306 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 17538964-7 2007 In particular, the presence of intracellular NS5A led to increased transcriptional and protein expression of IL-8 (CXCL-8), a chemokine with proinflammatory and anti-interferon properties, and impaired interferon induction of signal transducers and activators of transcription 1 (STAT1) serine and tyrosine and STAT2 tyrosine phosphorylation. Tyrosine 317-325 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 17420239-8 2007 Although many siderophores perturb labile cellular iron pools, only enterobactin elicits interleukin-8 secretion, suggesting that iron chelation is necessary but not sufficient. Enterobactin 68-80 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 17295217-7 2007 Furthermore, UTP had no effect on interleukin-(IL)-8 release and reduced the release of both CCL20 and IL-8 induced by TNF-alpha and LPS. Uridine Triphosphate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 17412724-2 2007 Clarithromycin initially decreases, then increases and finally produces a sustained suppression of interleukin (IL)-8 secretion from normal human bronchial epithelial (NHBE) cells through inhibition and activation of extracellular signal-regulated kinase (ERK). Clarithromycin 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 99-117 17306288-2 2007 In this work it is clarified how the presence of the alkali halides NaF, LiCl, NaCl, NaBr and NaI in the aqueous solutions, up to high molalities, change the lcb temperature-position and shape. halides 60-67 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 17577102-7 2007 Rosuvastatin inhibited the expressions of ICAM-1, MCP-1, IL-8, IL-6, and COX-2 mRNA and protein levels. Rosuvastatin Calcium 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 17372146-4 2007 The redistribution of PSGL-1 induced by IL-8 was inhibited by cholesterol-perturbing agents such as methyl-beta-cyclodextrin and filipin. Cholesterol 62-73 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17372146-4 2007 The redistribution of PSGL-1 induced by IL-8 was inhibited by cholesterol-perturbing agents such as methyl-beta-cyclodextrin and filipin. methyl-beta-cyclodextrin 100-124 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17372146-4 2007 The redistribution of PSGL-1 induced by IL-8 was inhibited by cholesterol-perturbing agents such as methyl-beta-cyclodextrin and filipin. Filipin 129-136 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17372146-8 2007 Treatment of neutrophils with IL-8 increased the formation of microaggregates composed of neutrophils and activated platelets, and this treatment also enhanced reactive oxygen species production in neutrophils induced by the cross-linking of PSGL-1 with antibodies. Reactive Oxygen Species 160-183 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 17314215-2 2007 In this study, we explored the effect of artesunate, an artemisinin derivative, on tumour necrosis factor (TNF)-alpha-induced production of interleukins, IL-1beta, IL-6 and IL-8, in human rheumatoid arthritis (RA) fibroblast-like synoviocytes (FLS), and further investigated the signal mechanism by which this compound modulates those cytokines" production. Artesunate 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 17314215-6 2007 RESULTS: Artesunate decreased the secretion of IL-1beta, IL-6 and IL-8 from TNF-alpha-stimulated RA FLS in a dose-dependent manner. Artesunate 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17314215-8 2007 The production of IL-1beta, IL-6 and IL-8 induced by TNF-alpha was decreased by pyrrolidine dithiocarbamate (PDTC), a chemical inhibitor of NF-kappaB. pyrrolidine dithiocarbamic acid 80-107 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 17314215-8 2007 The production of IL-1beta, IL-6 and IL-8 induced by TNF-alpha was decreased by pyrrolidine dithiocarbamate (PDTC), a chemical inhibitor of NF-kappaB. pyrrolidine dithiocarbamic acid 109-113 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 17314215-9 2007 These observations suggest that artesunate inhibits production of IL-1beta, IL-6 and IL-8 through inhibition of NF-kappaB signalling pathway. Artesunate 32-42 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17314215-11 2007 TNF-alpha-induced production of IL-1beta, IL-6 and IL-8 was hampered by treatment with the phosphatidylinositol 3 (PI3) kinase inhibitor LY294002, suggesting that inhibition of Akt activation might inhibit IL-1beta, IL-6 and IL-8 production induced by TNF-alpha. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 137-145 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 17314215-11 2007 TNF-alpha-induced production of IL-1beta, IL-6 and IL-8 was hampered by treatment with the phosphatidylinositol 3 (PI3) kinase inhibitor LY294002, suggesting that inhibition of Akt activation might inhibit IL-1beta, IL-6 and IL-8 production induced by TNF-alpha. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 137-145 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 17569118-5 2007 RESULTS: Acetate, propionate and butyrate at 30 mmol/L decreased LPS-stimulated TNFalpha release from neutrophils, without affecting IL-8 protein release. Butyrates 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 17524151-8 2007 Also, roxithromycin inhibited the SM-stimulated overproduction of the proinflammatory cytokines IL-1beta, IL-6, IL-8 and TNF at both the protein level and the mRNA level, as measured by either enzyme-linked immunosorbent assay (ELISA) or real-time RT-PCR. Roxithromycin 6-19 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 17524151-8 2007 Also, roxithromycin inhibited the SM-stimulated overproduction of the proinflammatory cytokines IL-1beta, IL-6, IL-8 and TNF at both the protein level and the mRNA level, as measured by either enzyme-linked immunosorbent assay (ELISA) or real-time RT-PCR. Mustard Gas 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 17218384-6 2007 In NB4 cells, ATRA treatment activates a novel signaling pathway, whereby interleukin-8 stimulates the expression of the homeobox transcription factor HOXA10v2, an effective enhancer of CYP26A1 transcription. Tretinoin 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 17355968-2 2007 By sensing the muramyl dipeptide (MDP), a bacterial wall component, NOD2 triggers the NF-kappaB signaling pathway and promotes the release of proinflammatory cytokines such as interleukin-8. Acetylmuramyl-Alanyl-Isoglutamine 15-32 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 17355968-2 2007 By sensing the muramyl dipeptide (MDP), a bacterial wall component, NOD2 triggers the NF-kappaB signaling pathway and promotes the release of proinflammatory cytokines such as interleukin-8. Acetylmuramyl-Alanyl-Isoglutamine 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 17543179-6 2007 ELISA was used to detect IL-8 secretion from THCEs challenged with ligands for TLR3 and TLR4 with and without antibody blockade. thces 45-50 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 17543179-13 2007 Blocking TLR4 with an anti-TLR4 antibody significantly inhibited the LPS-induced IL-8 production by THCE (P < 0.05). thce 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 17439270-5 2007 This phenomenon plays a critical role during the solidification process of NaCl-NaF melts of low NaF concentration and is demonstrated to account for the segregation of fluoride ions. Fluorides 169-177 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 17439270-5 2007 This phenomenon plays a critical role during the solidification process of NaCl-NaF melts of low NaF concentration and is demonstrated to account for the segregation of fluoride ions. Fluorides 169-177 C-X-C motif chemokine ligand 8 Homo sapiens 97-100 17397353-2 2007 It is now clear that macrolide antibiotics have anti-inflammatory effects, such as inhibition of IL-6, IL-8 and tumour necrosis factor-alpha, perhaps by suppressing the transcription factor nuclear factor-kappaB or activator protein-1, and reduction of neutrophil activity. Macrolides 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 103-140 17220369-4 2007 In this study we show a signaling pathway on the plasma surface of human airway epithelial NCI-H292 cells that regulate IL-8 production in response to a model inflammatory stimulus, phorbol 12-myristate 13-acetate, and a pathophysiological stimulus, gram-negative bacterial lipopolysaccharide. Tetradecanoylphorbol Acetate 182-213 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 17220369-8 2007 Last, we show that dual oxidase 1 (Duox1), a homolog of NADPH oxidase in airways, mediates TACE activation and IL-8 expression via generation of reactive oxygen species. Reactive Oxygen Species 145-168 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 17441793-8 2007 After 3 and 8 h of stimulation, codeine, but not meperidine, activated human mast cells to release monocyte chemoattractant protein-1 (CCL2), regulated on activation, normal T expressed and secreted (RANTES, CCL5) and interleukin-8 (CXCL 8) but not inducible protein-10 (CXCL10). Codeine 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 218-231 17441793-8 2007 After 3 and 8 h of stimulation, codeine, but not meperidine, activated human mast cells to release monocyte chemoattractant protein-1 (CCL2), regulated on activation, normal T expressed and secreted (RANTES, CCL5) and interleukin-8 (CXCL 8) but not inducible protein-10 (CXCL10). Codeine 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 233-239 17494953-3 2007 We applied cigarette smoke water extract (CSE) to primary human lung fibroblasts and found that CSE significantly increased CXC chemokine IL-8 production. Water 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 17224841-4 2007 Polymethylmethacrylate elicited a six- to 12-fold increase in gene expression of tumor necrosis factor alpha, interleukin 1alpha, interleukin 1beta, interleukin 6, and interleukin 8 in purified monocytes and unfractionated peripheral blood mononuclear cells. Polymethyl Methacrylate 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 168-181 17379503-6 2007 Treatment with the tyrosine kinase inhibitor gefitinib (Iressa) returned the expression levels of IL-8 and GRO back to the baseline observed in MCF-7 breast cancer cells, which express physiological levels of HER2. Gefitinib 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 17386409-5 2007 Panepoxydone strongly inhibited hTNF-alpha, IL-8 and NF-kappaB promoter activity in LPS/TPA stimulated MonoMac6 cells with IC(50) values of 0.5-1 microg/ml by blocking the phosphorylation of IkappaB and subsequent binding of the activated NF-kappaB transcription factor to the DNA. panepoxydone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17588137-5 2007 RESULTS: Quercetin decreased the gene expression and production of tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, IL-6, and IL-8 in PMACI-stimulated HMC-1 cells. Quercetin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 17460254-0 2007 Mitomycin C upregulates IL-8 and MCP-1 chemokine expression via mitogen-activated protein kinases in corneal fibroblasts. Mitomycin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 17353033-4 2007 Blocking neutrophil chemotactic factors such as leukotriene B(4) and IL-8 and related cysteine-X-cysteine chemokines by blocking receptor for leukotriene B(4) 1 and receptor for cysteine-X-cysteine chemokines 2 receptors is an approach that is currently being investigated. Leukotriene B4 48-61 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 17353033-4 2007 Blocking neutrophil chemotactic factors such as leukotriene B(4) and IL-8 and related cysteine-X-cysteine chemokines by blocking receptor for leukotriene B(4) 1 and receptor for cysteine-X-cysteine chemokines 2 receptors is an approach that is currently being investigated. cysteine-x-cysteine 86-105 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 17353033-4 2007 Blocking neutrophil chemotactic factors such as leukotriene B(4) and IL-8 and related cysteine-X-cysteine chemokines by blocking receptor for leukotriene B(4) 1 and receptor for cysteine-X-cysteine chemokines 2 receptors is an approach that is currently being investigated. Leukotrienes 48-59 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 17353033-4 2007 Blocking neutrophil chemotactic factors such as leukotriene B(4) and IL-8 and related cysteine-X-cysteine chemokines by blocking receptor for leukotriene B(4) 1 and receptor for cysteine-X-cysteine chemokines 2 receptors is an approach that is currently being investigated. cysteine-x-cysteine 178-197 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 17386409-5 2007 Panepoxydone strongly inhibited hTNF-alpha, IL-8 and NF-kappaB promoter activity in LPS/TPA stimulated MonoMac6 cells with IC(50) values of 0.5-1 microg/ml by blocking the phosphorylation of IkappaB and subsequent binding of the activated NF-kappaB transcription factor to the DNA. Tetradecanoylphorbol Acetate 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17460254-6 2007 RESULTS: The expression of IL-8 and MCP-1 were upregulated after MMC treatment in a time- and concentration-dependent manner. Mitomycin 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 17460254-9 2007 The MMC-related IL-8 and MCP-1 expression was inhibited by both a p38 inhibitor (SB203580) and an ERK inhibitor (PD98059). SB 203580 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 17460254-9 2007 The MMC-related IL-8 and MCP-1 expression was inhibited by both a p38 inhibitor (SB203580) and an ERK inhibitor (PD98059). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 113-120 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 17460254-11 2007 CONCLUSIONS: MMC treatment upregulated the expression of IL-8 and MCP-1 mRNA and protein secretion by the activation of mitogen-activated protein kinases (MAPKs) in corneal fibroblasts. Mitomycin 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 17124504-8 2007 This epoxide also induced pronounced DC activation indicated by upregulation of IL-8. Epoxy Compounds 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 17336340-7 2007 As well, hemin-induced IL-8 secretion was significantly reduced in a concentration-dependent fashion following pyrrolidine dithiocarbamate exposure, suggesting that induction occurred via an oxidant-sensitive mechanism. pyrrolidine dithiocarbamic acid 111-138 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 17207890-5 2007 TNF-alpha stimulated expression of both chemokines, while the PKCalpha/beta activator 12-O-tetradecanoyl-phorbol-13-acetate (TPA) induced only expression of IL-8 and inhibited TNF-alpha-induced RANTES expression. Tetradecanoylphorbol Acetate 86-123 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 17207890-5 2007 TNF-alpha stimulated expression of both chemokines, while the PKCalpha/beta activator 12-O-tetradecanoyl-phorbol-13-acetate (TPA) induced only expression of IL-8 and inhibited TNF-alpha-induced RANTES expression. Tetradecanoylphorbol Acetate 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 17207890-7 2007 In contrast, it decreased TNF-alpha or TPA-induced IL-8 release. Tetradecanoylphorbol Acetate 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 17207890-10 2007 An AP-1 and a NF-kappaB recognition sites were necessary for full induction of IL-8 promoter activity by TNF-alpha and TPA. Tetradecanoylphorbol Acetate 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 17442957-7 2007 Third, pharmacologic inhibition of PKC or PKD with Go6976 resulted in reduced expression and secretion of IL-8 and prevented the flagellin-induced activation of p38 MAPK, but treatment with the PKC inhibitor Go6983 had no significant effects on these phenotypes. Go 6976 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 17442957-7 2007 Third, pharmacologic inhibition of PKC or PKD with Go6976 resulted in reduced expression and secretion of IL-8 and prevented the flagellin-induced activation of p38 MAPK, but treatment with the PKC inhibitor Go6983 had no significant effects on these phenotypes. 2-(1-(3-dimethylaminopropyl)-5-methoxyindol-3-yl)-3-(1H-indol-3-yl)maleimide 208-214 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 17336340-0 2007 Hypoxia inducible factor-1 modulates hemin-induced IL-8 secretion in microvascular endothelium. Hemin 37-42 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 17336340-11 2007 Activation of HIF-1 via the prolyl hydroxylase inhibitor dimethyloxalylglycine attenuated hemin-induced IL-8 secretion. oxalylglycine 57-78 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 17511218-4 2007 In addition, it has been shown that bile acids and trypsin can promote IL-8 production from human esophageal epithelial cells via NFkappaB-and AP-1-dependent mechanism. Bile Acids and Salts 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 17262802-7 2007 RESULTS: Treatment with alpha-tocopherol succinate (VES) inhibits NF-kappaB but augments AP-1 activity, reduces expression of IL-6, IL-8, and VEGF, suppresses cell adhesion, ICAM-1 and gp130 expression in androgen-independent PC-3, DU-145, and CA-HPV-10 cells. alpha-Tocopherol 24-50 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 17400256-8 2007 In vitro, HES suppressed the expression of IL-8 on A549 cells and THP-1 cells, the expression of TNF-alpha, IL-1 beta, and IL-6 on THP-1 cells, the expression of ICAM-1 and VCAM-1 on A549 cells which effect cell adhesion function. Hesperidin 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 17400256-10 2007 HES inhibits those pathways, thereby suppressing the expression of IL-8, TNFalpha, IL-1 beta, IL-6, IL-12, ICAM-1 and VCAM-1. Hesperidin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 17164077-6 2007 Serum estradiol concentration showed a significant negative correlation with serum IL-6 concentration and weak negative correlations with serum concentrations of IL-2, IL-8 and GM-CSF. Estradiol 6-15 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 17306937-0 2007 The role of sphingosine 1-phosphate in the TNF-alpha induction of IL-8 gene expression in lung epithelial cells. sphingosine 1-phosphate 12-35 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17303577-4 2007 Here, we show the differential modulation of NF-kappaB activation and interleukin-8 (IL-8) expression in colonic epithelial cells HCT116 by saturated and unsaturated fatty acids mediated through Nods proteins. saturated and unsaturated fatty acids 140-177 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 17303577-4 2007 Here, we show the differential modulation of NF-kappaB activation and interleukin-8 (IL-8) expression in colonic epithelial cells HCT116 by saturated and unsaturated fatty acids mediated through Nods proteins. saturated and unsaturated fatty acids 140-177 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 17303577-5 2007 Lauric acid (C12:0) dose dependently activated NF-kappaB and induced IL-8 expression in HCT116 cells, which express both Nod1 and Nod2, but not detectable amounts of TLR2 and TLR4. lauric acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 17303577-8 2007 In contrast, polyunsaturated fatty acids, especially n-3 polyunsaturated fatty acids, inhibited the activation of NF-kappaB and IL-8 expression induced by lauric acid or known Nods ligands in HCT116. Fatty Acids, Unsaturated 13-40 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17303577-8 2007 In contrast, polyunsaturated fatty acids, especially n-3 polyunsaturated fatty acids, inhibited the activation of NF-kappaB and IL-8 expression induced by lauric acid or known Nods ligands in HCT116. Fatty Acids, Omega-3 53-84 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17303577-8 2007 In contrast, polyunsaturated fatty acids, especially n-3 polyunsaturated fatty acids, inhibited the activation of NF-kappaB and IL-8 expression induced by lauric acid or known Nods ligands in HCT116. lauric acid 155-166 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17439648-8 2007 Further, nanocurcumin"s mechanisms of action on pancreatic cancer cells mirror that of free curcumin, including induction of cellular apoptosis, blockade of nuclear factor kappa B (NFkappaB) activation, and downregulation of steady state levels of multiple pro-inflammatory cytokines (IL-6, IL-8, and TNFalpha). Curcumin 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 291-295 17404307-9 2007 Moreover, Pen c 13-mediated IL-8 release was significantly decreased in Ca(2+)-free medium and was abolished by the protease inhibitors, PMSF and 4-(2-aminoethyl) benzenesulfonyl fluoride. Phenylmethylsulfonyl Fluoride 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 17404307-9 2007 Moreover, Pen c 13-mediated IL-8 release was significantly decreased in Ca(2+)-free medium and was abolished by the protease inhibitors, PMSF and 4-(2-aminoethyl) benzenesulfonyl fluoride. 4-(2-aminoethyl)benzenesulfonylfluoride 146-187 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 17306937-3 2007 Although sphingolipids such as ceramide and sphingosine 1-phosphate (S1-P) have been shown to serve as signaling molecules in the TNF-alpha inflammatory response, their role in the TNF-alpha induction of IL-8 gene expression in lung epithelial cells is not known. Ceramides 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 17306937-3 2007 Although sphingolipids such as ceramide and sphingosine 1-phosphate (S1-P) have been shown to serve as signaling molecules in the TNF-alpha inflammatory response, their role in the TNF-alpha induction of IL-8 gene expression in lung epithelial cells is not known. sphingosine 1-phosphate 44-67 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 17306937-3 2007 Although sphingolipids such as ceramide and sphingosine 1-phosphate (S1-P) have been shown to serve as signaling molecules in the TNF-alpha inflammatory response, their role in the TNF-alpha induction of IL-8 gene expression in lung epithelial cells is not known. sphingosine 1-phosphate 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 17306937-4 2007 We investigated the role of sphingolipids in the TNF-alpha induction of IL-8 gene expression in H441 lung epithelial cells. Sphingolipids 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 17306937-7 2007 Dimethylsphingosine, an inhibitor of sphingosine kinase, partially inhibited TNF-alpha induction of IL-8 mRNA levels indicating the importance of intracellular increases in S1-P in the IL-8 induction. dimethylsphingosine 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 17306937-7 2007 Dimethylsphingosine, an inhibitor of sphingosine kinase, partially inhibited TNF-alpha induction of IL-8 mRNA levels indicating the importance of intracellular increases in S1-P in the IL-8 induction. dimethylsphingosine 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 17306937-3 2007 Although sphingolipids such as ceramide and sphingosine 1-phosphate (S1-P) have been shown to serve as signaling molecules in the TNF-alpha inflammatory response, their role in the TNF-alpha induction of IL-8 gene expression in lung epithelial cells is not known. Sphingolipids 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 17378789-7 2007 In these cases, the pain score decreased from 6.7 +/- 0.5 (mean +/- standard error of the mean) to 3.3 +/- 0.3 (P < 0.05), and the CSF concentrations of IL-8 and PGE(2) decreased significantly compared with pre-treatment levels (IL-8, 183.3 +/- 21.2 to 116.5 +/- 10.6 pg/ml; PGE(2), 43.8 +/- 10.3 to 14.7 +/- 3.0 pg/ml). Prostaglandins E 165-168 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 21730373-4 2007 Significant topographical changes were observed following exposure to aqueous solutions of ethylenediaminetetraacetic acid (EDTA) or highly concentrated sodium fluoride (NaF). Sodium Fluoride 153-168 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 17378789-7 2007 In these cases, the pain score decreased from 6.7 +/- 0.5 (mean +/- standard error of the mean) to 3.3 +/- 0.3 (P < 0.05), and the CSF concentrations of IL-8 and PGE(2) decreased significantly compared with pre-treatment levels (IL-8, 183.3 +/- 21.2 to 116.5 +/- 10.6 pg/ml; PGE(2), 43.8 +/- 10.3 to 14.7 +/- 3.0 pg/ml). Prostaglandins E 278-281 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 17378789-9 2007 CONCLUSION: Pain relief with intrathecal betamethasone is related to decreases in the CSF concentration of IL-8 and PGE(2). Betamethasone 41-54 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 17242997-1 2007 Using a cell stretcher device, we have previously shown that A549 cells exposed to asbestos fibers gave significantly increased cytokine responses (IL-8) when they were cyclically stretched [Tsuda, A., B. K. Stringer, S. M. Mijailovich, R. A. Rogers, K. Hamada, and M. L. Gray. Asbestos 83-91 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 17222322-6 2007 Serum beta-CTx correlated negatively with serum PIIINP and proinflammatory cytokines (IL-2, IL-6, IL-8, TNF-alpha), and positively with anti-inflammatory cytokines (IL-1, TGF-beta), whereas serum PIIINP correlated positively with these proinflammatory cytokines and negatively with the anti-inflammatory cytokines. beta-ctx 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 17242997-9 2007 Although it is generally assumed that riebeckite particles do not elicit strong biological responses, in our studies in cyclically stretched cell cultures, the riebeckite particles coated with adhesion proteins induced significant IL-8 responses, but in static cell cultures the treatment with adhesion protein-coated riebeckite did not induce comparable cytokine responses. Asbestos, Crocidolite 160-170 C-X-C motif chemokine ligand 8 Homo sapiens 231-235 17242997-9 2007 Although it is generally assumed that riebeckite particles do not elicit strong biological responses, in our studies in cyclically stretched cell cultures, the riebeckite particles coated with adhesion proteins induced significant IL-8 responses, but in static cell cultures the treatment with adhesion protein-coated riebeckite did not induce comparable cytokine responses. Asbestos, Crocidolite 160-170 C-X-C motif chemokine ligand 8 Homo sapiens 231-235 17576072-0 2007 Serum concentrations of interleukin-8 in relation to different levels of alcohol consumption. Alcohols 73-80 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 17240460-6 2007 Analysis of gene and protein expression determined a selectively increase of the pro-inflammatory cytokines monocyte chemoattractant protein (MCP)-1 and interleukin-8 (IL-8) following exposure to a pharmacological concentration of NFV and RTV. Nelfinavir 231-234 C-X-C motif chemokine ligand 8 Homo sapiens 153-166 17240460-6 2007 Analysis of gene and protein expression determined a selectively increase of the pro-inflammatory cytokines monocyte chemoattractant protein (MCP)-1 and interleukin-8 (IL-8) following exposure to a pharmacological concentration of NFV and RTV. Nelfinavir 231-234 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 17240460-6 2007 Analysis of gene and protein expression determined a selectively increase of the pro-inflammatory cytokines monocyte chemoattractant protein (MCP)-1 and interleukin-8 (IL-8) following exposure to a pharmacological concentration of NFV and RTV. Ritonavir 239-242 C-X-C motif chemokine ligand 8 Homo sapiens 153-166 17240460-6 2007 Analysis of gene and protein expression determined a selectively increase of the pro-inflammatory cytokines monocyte chemoattractant protein (MCP)-1 and interleukin-8 (IL-8) following exposure to a pharmacological concentration of NFV and RTV. Ritonavir 239-242 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 16984938-7 2007 Prednisolone markedly decreased IL8 and MMP1 expression compared with placebo, and the CIs excluded the likelihood of no effect. Prednisolone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 17383342-8 2007 RESULTS: Simvastatin significantly reduced the postoperative peak values of interleukin (IL)-6 and IL-8. Simvastatin 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 17339835-1 2007 In this issue of British Journal of Pharmacology, Megias and colleagues demonstrate how preincubation of human colonic Caco-2 cells with CORM-2, a carbon monoxide releasing molecule (CO-RM), reduces the expression of inducible nitric oxide synthase, interleukin (IL)-6 and IL-8 caused by proinflammatory cytokines. Carbon Monoxide 147-162 C-X-C motif chemokine ligand 8 Homo sapiens 273-277 17286758-5 2007 Cycloheximide reduced the UVB-mediated induction of IL-8 by 30-40%, suggesting that new protein synthesis contributed to IL-8 production. Cycloheximide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 17286758-5 2007 Cycloheximide reduced the UVB-mediated induction of IL-8 by 30-40%, suggesting that new protein synthesis contributed to IL-8 production. Cycloheximide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 17576072-2 2007 The present study was aimed at investigating serum IL-8 levels in relation to different levels of alcohol consumption. Alcohols 98-105 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 17576072-4 2007 The proportion of individuals with abnormally high (>10 pg/mL) IL-8 levels increased with alcohol use from 5.9% in abstainers to 10.7% in light, 13.2% in moderate, and 17.8% in heavy drinkers (P=0.004). Alcohols 93-100 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17576072-6 2007 Extremely high (>100 pg/mL) IL-8 levels were only observed among alcoholics, and were more frequent in females than in males (23.5% versus 9.7%, P=0.03) in spite of lower alcohol consumption among the former. Alcohols 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 17576072-7 2007 These data indicate that the effect of alcohol on serum IL-8 levels begins with light-to-moderate drinking and is dose-dependent. Alcohols 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 17576072-8 2007 Females may be more prone than males to develop extremely high IL-8 levels after heavy alcohol intake. Alcohols 87-94 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 17227950-6 2007 Levels of the angiogenic chemokine CXCL1 (mouse functional homologue of human IL-8) were found to be elevated in an adenosine-dependent manner in the lungs of ADA-deficient mice. Adenosine 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 17024463-0 2007 Identification of the dimerisation interface of human interleukin-8 by IL-8-variants containing the photoactivatable amino acid benzoyl-phenylalanine. amino acid benzoyl-phenylalanine 117-149 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 17024463-0 2007 Identification of the dimerisation interface of human interleukin-8 by IL-8-variants containing the photoactivatable amino acid benzoyl-phenylalanine. amino acid benzoyl-phenylalanine 117-149 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 17024463-4 2007 In order to obtain a better understanding of the dimerisation process, covalently linked homo- and heterodimers were produced by photo-induced dimerisation of hIL-8 analogues that contain the photo-activatable amino acid p-benzoyl-phenylalanine (Bpa) at different positions. amino acid p-benzoyl-phenylalanine 210-244 C-X-C motif chemokine ligand 8 Homo sapiens 159-164 17024463-4 2007 In order to obtain a better understanding of the dimerisation process, covalently linked homo- and heterodimers were produced by photo-induced dimerisation of hIL-8 analogues that contain the photo-activatable amino acid p-benzoyl-phenylalanine (Bpa) at different positions. 4-benzoylphenylalanine 246-249 C-X-C motif chemokine ligand 8 Homo sapiens 159-164 17024463-6 2007 The segments were combined by expressed protein ligation and led to full length IL-8 variants containing the non-proteinogenic amino acid Bpa at single positions. 4-benzoylphenylalanine 138-141 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 17359338-7 2007 Cadexomer and cadexomer iodine significantly increased the expression of IL-1 beta, IL-8, TNF-alpha and VEGF mRNA, while they did not affect that of IL-6, IL-10, IL-12 p 40 or bFGF mRNA. Iodine 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 17873318-7 2007 However, in linear regression analysis, BMI, diastolic blood pressure, glucose, insulin, and IL-8 emerged as significant predictors of ADMA. N,N-dimethylarginine 135-139 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 16952401-8 2007 In conclusion, MgSO(4) inhibits endothelial cell activation, as measured by levels of IL-8 and ICAM-1 expression, via NFkappaB. mgso 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 16900358-3 2007 Supernatants of histamine-stimulated cells were evaluated for the production of IL-6 and IL-8 by ELISA, while the expression of ICAM-1 was evaluated by flow cytometry on IFN gamma-stimulated cells. Histamine 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 17414009-1 2007 PURPOSE: Skeletal positron emission tomography (PET) with fluorine-18 (18F) sodium fluoride (18F NaF) is an alternative to technetium-99m (99mTc)methylene diphosphonate (MDP) scintigraphy. fluorine-18 (18f) sodium fluoride 58-91 C-X-C motif chemokine ligand 8 Homo sapiens 97-100 17384028-6 2007 Fluoride had a biphasic effect on cell proliferation, with enhanced proliferation at 16 microM, and reduced proliferation at greater than 1 mM F. Flow cytometry showed that both 10 microM and 20 microM NaF significantly increased the apoptotic index of ameloblast-lineage cells. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 202-205 17118622-7 2007 Also, TNF-alpha and IL-8 secretion were markedly induced by DNCB and NiSO(4) in a dose-dependent manner. Dinitrochlorobenzene 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 17431105-9 2007 Tumors from animals treated with liposomal curcumin showed an antiangiogenic effect, including attenuation of CD31 (an endothelial marker), vascular endothelial growth factor, and interleukin-8 expression by immunohistochemistry. Curcumin 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 17118622-7 2007 Also, TNF-alpha and IL-8 secretion were markedly induced by DNCB and NiSO(4) in a dose-dependent manner. niso 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 17307163-5 2007 However, activation with PGD2 in the presence of tumor necrosis factor (TNF)-alpha mediated significant production of MCP-1 and IL-8, but not the other cytokines and chemokines, in comparison to single stimulation with TNF-alpha. Prostaglandin D2 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 17628972-6 2007 RESULTS: IL-5, IL-6 and IL-8 levels in both AR and NAR groups were significantly elevated compared with normal group (all P < 0.01 for AR group; P < 0.05, 0.05, 0.01 for NAR group, respectively), and they were much higher in AR group in comparison with NAR group (P < 0.01, 0.05, 0.01, respectively). Argon 44-46 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 17628972-6 2007 RESULTS: IL-5, IL-6 and IL-8 levels in both AR and NAR groups were significantly elevated compared with normal group (all P < 0.01 for AR group; P < 0.05, 0.05, 0.01 for NAR group, respectively), and they were much higher in AR group in comparison with NAR group (P < 0.01, 0.05, 0.01, respectively). Argon 52-54 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 17307163-0 2007 Synergistic effect of PGD2 via prostanoid DP receptor on TNF-alpha-induced production of MCP-1 and IL-8 in human monocytic THP-1 cells. Prostaglandin D2 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 17307163-6 2007 In addition, the selective prostanoid DP receptor antagonist, pinagladin ((Z)-7-[(1R,2R,3S,5S)-2-(benzothiophen-3-ylcarbonylamide)-10-norpinan-3-yl]hept-5-enoic acid) inhibited the production of MCP-1 and IL-8 upon combined stimulation with PGD2 and TNF-alpha. pinagladin 62-72 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 17307163-6 2007 In addition, the selective prostanoid DP receptor antagonist, pinagladin ((Z)-7-[(1R,2R,3S,5S)-2-(benzothiophen-3-ylcarbonylamide)-10-norpinan-3-yl]hept-5-enoic acid) inhibited the production of MCP-1 and IL-8 upon combined stimulation with PGD2 and TNF-alpha. (Z)-7-((1R,2R,3S,5S)-2-(benzothiophen-3-ylcarbonylamide)-10-norpinan-3-yl)hept-5-enoic acid 74-165 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 17307163-7 2007 The synergistic production of MCP-1 and IL-8 by PGD2 was mimicked by dibutyryl cAMP (db-cAMP) and was inhibited by a protein kinase A (PKA) inhibitor. Prostaglandin D2 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17307163-7 2007 The synergistic production of MCP-1 and IL-8 by PGD2 was mimicked by dibutyryl cAMP (db-cAMP) and was inhibited by a protein kinase A (PKA) inhibitor. Bucladesine 69-83 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17307163-7 2007 The synergistic production of MCP-1 and IL-8 by PGD2 was mimicked by dibutyryl cAMP (db-cAMP) and was inhibited by a protein kinase A (PKA) inhibitor. Bucladesine 85-92 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17307163-8 2007 Our findings suggest that activation of the prostanoid DP receptor on THP-1 cells enhances TNF-alpha-induced MCP-1 and IL-8 production via the cAMP/PKA signaling pathway. Cyclic AMP 143-147 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 16860297-7 2007 Exposure to the photochemically generated products of BD (primarily acrolein, acetaldehyde, formaldehyde, furan and ozone) induced significant increases in cytotoxicity, IL-8, and IL-6 gene expression compared to a synthetic mixture of primary products that was created by injecting the correct concentrations of the detected products from the irradiation experiments. Acrolein 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 20641299-0 2004 (99m)Tc-Hydrazinonicotinamide-interleukin-8 Interleukin-8 (IL-8) has a molecular mass of 8.5 kDa and is an inflammatory chemokine secreted by many cell types (1). tc-hydrazinonicotinamide 5-29 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 20641299-0 2004 (99m)Tc-Hydrazinonicotinamide-interleukin-8 Interleukin-8 (IL-8) has a molecular mass of 8.5 kDa and is an inflammatory chemokine secreted by many cell types (1). tc-hydrazinonicotinamide 5-29 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 20641299-6 2004 The ready availability and low cost of (99m)Tc led to the development of (99m)Tc-IL-8 for studying activated leukocytes in inflamed and infective tissues (3-8). Technetium 44-46 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 17375198-9 2007 MMP-8 cleaves CXCL8 at Arg(5)-Ser(6) and at Val(7)-Leu(8) in CXCL5 to activate respective chemokines. Arginine 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 16860297-7 2007 Exposure to the photochemically generated products of BD (primarily acrolein, acetaldehyde, formaldehyde, furan and ozone) induced significant increases in cytotoxicity, IL-8, and IL-6 gene expression compared to a synthetic mixture of primary products that was created by injecting the correct concentrations of the detected products from the irradiation experiments. Acetaldehyde 78-90 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 17375198-9 2007 MMP-8 cleaves CXCL8 at Arg(5)-Ser(6) and at Val(7)-Leu(8) in CXCL5 to activate respective chemokines. Serine 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 16860297-7 2007 Exposure to the photochemically generated products of BD (primarily acrolein, acetaldehyde, formaldehyde, furan and ozone) induced significant increases in cytotoxicity, IL-8, and IL-6 gene expression compared to a synthetic mixture of primary products that was created by injecting the correct concentrations of the detected products from the irradiation experiments. Ozone 116-121 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 17339475-5 2007 CoMTb-induced prolonged dose-dependent, p38-mediated expression of stable CXCL8 mRNA by fibroblasts accompanied by a >10-fold increase in CXCL8 secretion (487 +/- 88 ng/ml vs 48.6 +/- 34 ng/ml in controls) at 120 h. Fibroblasts strongly expressed CXCL8 in vivo in human TB granulomas. comtb 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 74-79 17339475-5 2007 CoMTb-induced prolonged dose-dependent, p38-mediated expression of stable CXCL8 mRNA by fibroblasts accompanied by a >10-fold increase in CXCL8 secretion (487 +/- 88 ng/ml vs 48.6 +/- 34 ng/ml in controls) at 120 h. Fibroblasts strongly expressed CXCL8 in vivo in human TB granulomas. comtb 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 141-146 17339475-5 2007 CoMTb-induced prolonged dose-dependent, p38-mediated expression of stable CXCL8 mRNA by fibroblasts accompanied by a >10-fold increase in CXCL8 secretion (487 +/- 88 ng/ml vs 48.6 +/- 34 ng/ml in controls) at 120 h. Fibroblasts strongly expressed CXCL8 in vivo in human TB granulomas. comtb 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 141-146 17339489-7 2007 The stimulatory role was confirmed by the observation that 12.5 microM H(2)O(2), a concentration found during inflammation, increased the expression of several proinflammatory NF-kappaB-dependent genes induced by TNF-alpha (e.g., IL-8, MCP-1, TLR2, and TNF-alpha). Water 71-77 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 17095757-0 2007 Carrageenan induces interleukin-8 production through distinct Bcl10 pathway in normal human colonic epithelial cells. Carrageenan 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 20-33 17293063-6 2007 Genes up-regulated by selenium supplementation included TNF, IL1B, IL8, SOD2, CXCL2 and several other immunological and oxidative stress-related genes. Selenium 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 17095757-5 2007 Increased Bcl10, nuclear and cytoplasmic NF-kappaB, IL-8 promoter activation, and IL-8 secretion were detected following carrageenan exposure. Carrageenan 121-132 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 17095757-5 2007 Increased Bcl10, nuclear and cytoplasmic NF-kappaB, IL-8 promoter activation, and IL-8 secretion were detected following carrageenan exposure. Carrageenan 121-132 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 17095757-6 2007 Knockdown of Bcl10 by siRNA markedly reduced the increase in IL-8 that followed carrageenan exposure in the NCM460 cells. Carrageenan 80-91 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 17095757-7 2007 These results show, for the first time, that exposure of human intestinal epithelial cells to carrageenan triggers a distinct inflammatory pathway via activation of Bcl10 with NF-kappaB activation and upregulation of IL-8 secretion. Carrageenan 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 17138957-9 2007 The NO donor S-nitroso-N-acetyl-d,l-penicillamine inhibited CXCL8-induced human neutrophil chemotaxis and CXCR2 expression on human and murine neutrophils. snap 13-49 C-X-C motif chemokine ligand 8 Homo sapiens 60-65 17158355-3 2007 METHODS AND RESULTS: Treatment of endothelial cells with anthocyanin prevented from CD40-induced proinflammatory status, measured by production of IL-6, IL-8, and monocyte chemoattractant protein-1 through inhibiting CD40-induced nuclear factor-kappaB (NF-kappaB) activation. Anthocyanins 57-68 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 17235257-15 2007 CONCLUSIONS: IL-8 and GRO-alpha secreted from alveolar epithelial cells play an important role in the cell-cell interaction involved in the chemotactic transmigration of ATRA-treated APL cells toward alveolar epithelial cells. Tretinoin 170-174 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 17453947-11 2007 They also enhanced IL-8 gene expression and IL-8 protein secretion in the following decreasing order: 25-hydroxycholesterol > 24-hydroxycholesterol > 7-ketocholesterol. 25-hydroxycholesterol 102-123 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 17453947-11 2007 They also enhanced IL-8 gene expression and IL-8 protein secretion in the following decreasing order: 25-hydroxycholesterol > 24-hydroxycholesterol > 7-ketocholesterol. 25-hydroxycholesterol 102-123 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17235257-0 2007 Role of interleukin-8 and growth-regulated oncogene-alpha in the chemotactic migration of all-trans retinoic acid-treated promyelocytic leukemic cells toward alveolar epithelial cells. Tretinoin 100-113 C-X-C motif chemokine ligand 8 Homo sapiens 8-21 17235257-2 2007 We investigated the role of interleukin (IL)-8 and growth-regulated oncogene (GRO)-alpha in the chemotactic transmigration of ATRA-treated NB4 (ATRA-NB4) APL cells toward A549 alveolar epithelial cells. Tretinoin 126-130 C-X-C motif chemokine ligand 8 Homo sapiens 28-46 17364953-0 2007 25-Hydroxycholesterol, 7beta-hydroxycholesterol and 7-ketocholesterol upregulate interleukin-8 expression independently of Toll-like receptor 1, 2, 4 or 6 signalling in human macrophages. 25-hydroxycholesterol 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 17235257-10 2007 Only A549 cells constitutively secreted GRO-alpha, and both A549 and NB4 cells constitutively secreted IL-8, which was enhanced by ATRA. Tretinoin 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 17359210-1 2007 AIM: Aim of the present study was to evaluate the salivary clearance of Fluoride following administration of tablets and chewing gums containing 0.50 mg of Fluoride in the form of NaF. Fluorides 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 17359210-1 2007 AIM: Aim of the present study was to evaluate the salivary clearance of Fluoride following administration of tablets and chewing gums containing 0.50 mg of Fluoride in the form of NaF. Fluorides 156-164 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 17453947-11 2007 They also enhanced IL-8 gene expression and IL-8 protein secretion in the following decreasing order: 25-hydroxycholesterol > 24-hydroxycholesterol > 7-ketocholesterol. 24-hydroxycholesterol 129-150 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 17453947-11 2007 They also enhanced IL-8 gene expression and IL-8 protein secretion in the following decreasing order: 25-hydroxycholesterol > 24-hydroxycholesterol > 7-ketocholesterol. 7-ketocholesterol 156-173 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 17621943-3 2007 In artificial saliva containing 0.1% NaF at a pH of 4.0, the amounts of Ti dissolved from the Ti, Ti-6Al-4V, and Ti-6Al-7Nb alloys were about 50 times larger than those of the alloys containing 0.5 wt% Pt. Platinum 202-204 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 17286808-8 2007 In addition, secretion of proinflammatory mediators such as the cytokines interleukin-1beta (IL-1beta), tumor necrosis factor-alpha (TNF alpha), IL-6 and IL-8 were inhibited in the presence of physiological doses of OMZ. Oxymetazoline 216-219 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 17364953-0 2007 25-Hydroxycholesterol, 7beta-hydroxycholesterol and 7-ketocholesterol upregulate interleukin-8 expression independently of Toll-like receptor 1, 2, 4 or 6 signalling in human macrophages. cholest-5-en-3 beta,7 alpha-diol 23-47 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 17364953-0 2007 25-Hydroxycholesterol, 7beta-hydroxycholesterol and 7-ketocholesterol upregulate interleukin-8 expression independently of Toll-like receptor 1, 2, 4 or 6 signalling in human macrophages. 7-ketocholesterol 52-69 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 17364953-3 2007 Each oxysterol stimulated secretion of the inflammatory chemokine interleukin-8 (IL-8), but not IkappaBalpha degradation or tumour necrosis factor-alpha release from monocytic THP-1 cells. Oxysterols 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 17364953-3 2007 Each oxysterol stimulated secretion of the inflammatory chemokine interleukin-8 (IL-8), but not IkappaBalpha degradation or tumour necrosis factor-alpha release from monocytic THP-1 cells. Oxysterols 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 17406807-2 2007 METHODS: Neutrophils were incubated with different concentrations of omeprazole and pantoprazole for 30 min and stimulated to migrate with fMLP and IL-8. Omeprazole 69-79 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 16715250-0 2007 (E)-metanicotine hemigalactarate (TC-2403-12) inhibits IL-8 production in cells of the inflamed mucosa. (e)-metanicotine hemigalactarate 0-32 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 16715250-0 2007 (E)-metanicotine hemigalactarate (TC-2403-12) inhibits IL-8 production in cells of the inflamed mucosa. metanicotine 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 17406807-2 2007 METHODS: Neutrophils were incubated with different concentrations of omeprazole and pantoprazole for 30 min and stimulated to migrate with fMLP and IL-8. Pantoprazole 84-96 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 16715250-8 2007 RESULTS: In MM6 cells, IL-8 secretion was significantly decreased to 30% of control after TC-2403-12 treatment, with best results after pretreatment for 24 h. This decrease in cell activation was not due to apoptosis and was not mediated by inhibition of NF-kappaB activation. metanicotine 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 16715250-9 2007 IL-8 production in neutrophils and primary CEC also tended to be decreased after TC-2403-12 treatment. metanicotine 81-91 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 17406807-6 2007 RESULTS: Omeprazole is able to inhibit neutrophil chemotaxis to fMLP and IL-8. Omeprazole 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 16715250-11 2007 CONCLUSION: TC-2403-12 effectively inhibited TNF- and LPS-induced IL-8 production in different cell types. metanicotine 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17273783-6 2007 Moreover, the intracellular levels and secretion rates of IL-8 were also markedly reduced in the protein extracts and conditioned media of CW-DMEM-incubated keratinocytes. dmem 142-146 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 17430259-11 2007 Olprinone inhibited the increase in the IL-8 levels resulting from the incubation of HK-2 with TNF-alpha. olprinone 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17273783-7 2007 Notably, the most effective inhibition of IL-8 secretion was elicited by a 25% CW fraction in the DMEM. dmem 98-102 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 17273783-0 2007 Comano"s (Trentino) thermal water interferes with tumour necrosis factor-alpha expression and interleukin-8 production and secretion by cultured human psoriatic keratinocytes: yet other mechanisms of its anti-psoriatic action. trentino 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 17273783-0 2007 Comano"s (Trentino) thermal water interferes with tumour necrosis factor-alpha expression and interleukin-8 production and secretion by cultured human psoriatic keratinocytes: yet other mechanisms of its anti-psoriatic action. Water 28-33 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 17008880-0 2007 Regulation of UVB-induced IL-8 and MCP-1 production in skin keratinocytes by increasing vitamin C uptake via the redistribution of SVCT-1 from the cytosol to the membrane. Ascorbic Acid 88-97 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 17314256-6 2007 Furthermore, human monocytes stimulated by water-insoluble alpha-glucans produced TNF-alpha and IL-8, while human polymorphonuclear cells were activated by water-insoluble alpha-glucans, resulting in chemotaxis and hydrogen peroxide production. Water 43-48 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 17314256-6 2007 Furthermore, human monocytes stimulated by water-insoluble alpha-glucans produced TNF-alpha and IL-8, while human polymorphonuclear cells were activated by water-insoluble alpha-glucans, resulting in chemotaxis and hydrogen peroxide production. alpha-glucans 59-72 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 17454250-4 2007 MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) cell viability decreased significantly (p < .05) from 0.00005 to 0.05 mg/ml after 24 h. The proinflammatory mediators of inflammation cytokines interleukin (IL)-6, IL-8, tumor necrosis factor (TNF)-alpha, IL-10, and IL-1beta were also assessed. monooxyethylene trimethylolpropane tristearate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 17454250-4 2007 MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) cell viability decreased significantly (p < .05) from 0.00005 to 0.05 mg/ml after 24 h. The proinflammatory mediators of inflammation cytokines interleukin (IL)-6, IL-8, tumor necrosis factor (TNF)-alpha, IL-10, and IL-1beta were also assessed. thiazolyl blue 5-65 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 17008880-7 2007 In addition, increased IL-8 and MCP-1 mRNA expressions were suppressed by vitamin C treatment. Ascorbic Acid 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 17008880-9 2007 Taken together, vitamin C uptake is increased in UVB-irradiated keratinocytes through the translocation of SVCT-1 and regulates inflammatory response in the skin via the downregulation of IL-8 and MCP-1 production. Ascorbic Acid 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 17039239-3 2007 Notably, extracellular ATP displayed a complex regulation of IFN-gamma-stimulated chemokine expression, with upregulation of CC chemokine ligand 2 (CCL2), CCL5 and CXC chemokine ligand 8 (CXCL8), and suppression of the receptor CXC chemokine receptor 3 (CXCR3), CXCL9, CXCL10, and CXCL11. Adenosine Triphosphate 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 164-186 17130184-9 2007 The inhibitors of PI-3K wortmannin and LY294002 inhibited the chemotaxis and suppressed IL-8-evoked dephosphorylation and rephosphorylation of cofilin. Wortmannin 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 17039239-3 2007 Notably, extracellular ATP displayed a complex regulation of IFN-gamma-stimulated chemokine expression, with upregulation of CC chemokine ligand 2 (CCL2), CCL5 and CXC chemokine ligand 8 (CXCL8), and suppression of the receptor CXC chemokine receptor 3 (CXCR3), CXCL9, CXCL10, and CXCL11. Adenosine Triphosphate 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 188-193 17130184-9 2007 The inhibitors of PI-3K wortmannin and LY294002 inhibited the chemotaxis and suppressed IL-8-evoked dephosphorylation and rephosphorylation of cofilin. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 17332609-2 2007 Previous studies with various animal models showed that (99m)Tc-labeled IL-8 accumulates specifically and rapidly in infectious and inflammatory foci. Technetium 61-63 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 17043099-4 2007 RESULTS: Polyriboinosinic:polyribocytidylic acid (poly I:C), a synthetic dsRNA that antagonizes TLR3, stimulated the secretion of IL-6, IL-8 and GCP-2 by OECs. Poly I-C 9-48 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 17081611-8 2007 Parotid saliva augmented IL-8 production of THP-1 cells stimulated with a synthetic TLR2 ligand, Pam(3)Cys-Ser-(Lys)(4) (Pam(3)CSK(4)). Cysteine 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 17081611-8 2007 Parotid saliva augmented IL-8 production of THP-1 cells stimulated with a synthetic TLR2 ligand, Pam(3)Cys-Ser-(Lys)(4) (Pam(3)CSK(4)). Serine 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 17081611-8 2007 Parotid saliva augmented IL-8 production of THP-1 cells stimulated with a synthetic TLR2 ligand, Pam(3)Cys-Ser-(Lys)(4) (Pam(3)CSK(4)). Lysine 112-115 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 17182620-1 2007 Activation of CD38 in lymphokine-activated killer (LAK) cells involves interleukin-8 (IL8)-mediated protein kinase G (PKG) activation and results in an increase in the sustained intracellular Ca(2+) concentration ([Ca(2+)](i)), cADP-ribose, and LAK cell migration. Cyclic ADP-Ribose 228-239 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 17182620-1 2007 Activation of CD38 in lymphokine-activated killer (LAK) cells involves interleukin-8 (IL8)-mediated protein kinase G (PKG) activation and results in an increase in the sustained intracellular Ca(2+) concentration ([Ca(2+)](i)), cADP-ribose, and LAK cell migration. Cyclic ADP-Ribose 228-239 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 17182620-6 2007 Supporting these observations, IL8- or cell-permeable cGMP analog-induced formation of cADP-ribose, increase in [Ca(2+)](i), and migration of LAK cells were inhibited by treatment with the MHCIIA inhibitor blebbistatin. Cyclic GMP 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 17182620-6 2007 Supporting these observations, IL8- or cell-permeable cGMP analog-induced formation of cADP-ribose, increase in [Ca(2+)](i), and migration of LAK cells were inhibited by treatment with the MHCIIA inhibitor blebbistatin. Cyclic ADP-Ribose 87-98 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 17182620-6 2007 Supporting these observations, IL8- or cell-permeable cGMP analog-induced formation of cADP-ribose, increase in [Ca(2+)](i), and migration of LAK cells were inhibited by treatment with the MHCIIA inhibitor blebbistatin. blebbistatin 206-218 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 17301742-3 2007 claim that Naf-BBL--a naphthylalanine-labelled, truncated version of this domain--folds in this way, on the grounds that they recorded a wide spread of melting temperatures of individual atoms measured by proton nuclear magnetic resonance (NMR) during their thermal denaturation. naphthylalanine 22-37 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 17301743-3 2007 claim that the small re-engineered protein Naf-BBL unfolds without significant cooperativity or kinetic hindrance, a conclusion that is based on calculation of a broad distribution of midpoint thermal-transition temperatures measured by the nuclear magnetic resonance (NMR) chemical shifts of 158 protons. N-Carbobenzyloxy-L-alanine 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 16928771-0 2007 Protein kinase D2 mediates lysophosphatidic acid-induced interleukin 8 production in nontransformed human colonic epithelial cells through NF-kappaB. lysophosphatidic acid 27-48 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 16928771-1 2007 The signaling pathways mediating lysophosphatidic acid (LPA)-stimulated PKD(2) activation and the potential contribution of PKD(2) in regulating LPA-induced interleukin 8 (IL-8) secretion in nontransformed, human colonic epithelial NCM460 cells were examined. lysophosphatidic acid 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 157-170 16928771-1 2007 The signaling pathways mediating lysophosphatidic acid (LPA)-stimulated PKD(2) activation and the potential contribution of PKD(2) in regulating LPA-induced interleukin 8 (IL-8) secretion in nontransformed, human colonic epithelial NCM460 cells were examined. lysophosphatidic acid 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 16928771-1 2007 The signaling pathways mediating lysophosphatidic acid (LPA)-stimulated PKD(2) activation and the potential contribution of PKD(2) in regulating LPA-induced interleukin 8 (IL-8) secretion in nontransformed, human colonic epithelial NCM460 cells were examined. lysophosphatidic acid 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 157-170 16928771-1 2007 The signaling pathways mediating lysophosphatidic acid (LPA)-stimulated PKD(2) activation and the potential contribution of PKD(2) in regulating LPA-induced interleukin 8 (IL-8) secretion in nontransformed, human colonic epithelial NCM460 cells were examined. lysophosphatidic acid 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 16928771-5 2007 LPA induced a striking increase in IL-8 production and stimulated NF-kappaB activation, as measured by NF-kappaB-DNA binding, NF-kappaB-driven luciferase reporter activity, and IkappaBalpha phosphorylation. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 16928771-7 2007 PKD(2) activation is a novel early event in the biological action of LPA and mediates LPA-stimulated IL-8 secretion in NCM460 cells through a NF-kappaB-dependent pathway. lysophosphatidic acid 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 17169865-2 2007 We have recently reported that early changes in NO2-exposed human bronchial epithelial cells are causally linked to increased generation of proinflammatory mediators, such as nitric oxide/nitrite and cytokines like interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha and IL-8. Nitrogen Dioxide 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 277-281 17227815-5 2007 Pretreatment of cervical stromal cells with inhibitors of RhoA (C3 transferase exoenzyme), Rho-kinase (Y-27632) or NF-kB (BAY11-7082) effectively blocked LPS-induced IL-8 release. 3-(4-methylphenylsulfonyl)-2-propenenitrile 122-132 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 17227815-6 2007 In contrast, IL-1beta-induced IL-8 production was significantly blocked by BAY11-7082, but not by C3 transferase exoenzyme or Y-27632. 3-(4-methylphenylsulfonyl)-2-propenenitrile 75-85 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 17326846-2 2007 This study measured cytotoxicity and the release of the proinflammatory cytokines IL-6 and IL-8 by human bronchial epithelial cells treated with manufactured nano- and micron-sized particles of Al2O3, CeO2, Fe2O3, NiO, SiO2, and TiO2, with soil-derived particles from fugitive dust sources, and with the positive controls LPS, TNF-alpha, and VOSO4. Aluminum Oxide 194-199 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 17277122-7 2007 Human immature dendritic cells (DCs) cultured in the presence of c-di-GMP showed increased expression of costimulatory molecules CD80/CD86 and maturation marker CD83, increased MHC class II and cytokines and chemokines such as IL-12, IFN-gamma, IL-8, MCP-1, IFN-gamma-inducible protein 10, and RANTES, and altered expression of chemokine receptors including CCR1, CCR7, and CXCR4. bis(3',5')-cyclic diguanylic acid 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 17178391-8 2007 Selective inhibitors of p38(mapk) (SB203580) or of MEK1/2, the direct upstream activator of ERK1/2 (PD98059), reduced the synthesis of IL-1beta, TNFalpha, IL-6 and IL-8 induced by either the chaperonins or LPS. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 100-107 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 17043099-4 2007 RESULTS: Polyriboinosinic:polyribocytidylic acid (poly I:C), a synthetic dsRNA that antagonizes TLR3, stimulated the secretion of IL-6, IL-8 and GCP-2 by OECs. Poly I-C 50-58 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 17203209-2 2007 Recently, increase in interleukin (IL)-8 in the esophageal mucosa has been associated with the pathogenesis of esophagitis induced by reflux of gastric acids, bile acids or trypsin. Bile Acids and Salts 159-169 C-X-C motif chemokine ligand 8 Homo sapiens 22-40 17289483-10 2007 DEX significantly reduced at least 1 postoperative level of IL-6, IL-8, IL-10, CRP, and exhaled NO. Dexamethasone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 17203209-5 2007 IL-8 was produced in a dose-dependent fashion when cells were stimulated with a PAR2 agonist such as trypsin or SLIGKV-amide. Amides 119-124 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 17125827-10 2007 In contrast, histamine rapidly induced a Ca(2+) signal and stimulated IL-8 production in MDMs. Histamine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17121804-0 2007 Rhinovirus activates interleukin-8 expression via a Src/p110beta phosphatidylinositol 3-kinase/Akt pathway in human airway epithelial cells. Phosphatidylinositols 65-85 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 17237377-5 2007 We also show that HP-NAP stimulates human PMNs to synthesize and release a number of chemokines, including CXCL8, CCL3, and CCL4. hp-nap 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 107-112 17237435-6 2007 Prednisolone dose-dependently inhibited the LPS-induced release of cytokines (TNF-alpha and IL-6) and chemokines (IL-8 and MCP-1), while enhancing the release of the anti-inflammatory cytokine IL-10. Prednisolone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 17108260-4 2007 These genes were also found to be NF-kappaB-dependent in that TNFalpha-induced expression of IL-6, IL-8, and eotaxin was dose-dependently inhibited by the selective IKKbeta inhibitor 4-(2"-aminoethyl)amino-1,8-dimethylimidazo[1,2-a]quinoxaline (BMS-345541) (1-30 microM). 4(2'-aminoethyl)amino-1,8-dimethylimidazo(1,2-a)quinoxaline 183-243 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 16806476-0 2007 Saxatilin inhibits TNF-alpha-induced proliferation by suppressing AP-1-dependent IL-8 expression in the ovarian cancer cell line MDAH 2774. saxatilin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 16806476-3 2007 TNF-alpha-induced IL-8 promoter activation that is inhibited by saxatilin treatment was dependent on activating protein-1 (AP-1) instead of nuclear factor-kappa B (NF-kappaB). saxatilin 64-73 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 16806476-4 2007 Coexpression of dominant negative p38 (DN-p38) suggested that p38 is involved in the IL-8 promoter activity which is regulated by saxatilin or TNF-alpha. saxatilin 130-139 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 16806476-5 2007 Experimental evidence clearly indicated that saxatilin inhibits TNF-alpha-induced proliferation of the ovarian cancer cells by suppressing IL-8 expression in AP-1-dependent manner. saxatilin 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 16712933-8 2007 125I-labeled hIL-8 bound to gpCXCR1 and addition of unlabeled hIL-8 completely abolished the binding; however, unlabeled gpIL-8 failed to compete against 125I-labeled hIL-8, strongly suggesting that the avidity of hIL-8 to gpCXCR1 is higher than that of gpIL-8. Iodine-125 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-18 16712933-8 2007 125I-labeled hIL-8 bound to gpCXCR1 and addition of unlabeled hIL-8 completely abolished the binding; however, unlabeled gpIL-8 failed to compete against 125I-labeled hIL-8, strongly suggesting that the avidity of hIL-8 to gpCXCR1 is higher than that of gpIL-8. gpil-8 254-260 C-X-C motif chemokine ligand 8 Homo sapiens 13-18 17108260-4 2007 These genes were also found to be NF-kappaB-dependent in that TNFalpha-induced expression of IL-6, IL-8, and eotaxin was dose-dependently inhibited by the selective IKKbeta inhibitor 4-(2"-aminoethyl)amino-1,8-dimethylimidazo[1,2-a]quinoxaline (BMS-345541) (1-30 microM). 4(2'-aminoethyl)amino-1,8-dimethylimidazo(1,2-a)quinoxaline 245-255 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 17286914-7 2007 The combination of TBP and TRBP was able to obviously inhibit both respiratory burst of monocytes induced by TNF-alpha and IFN-gamma and transcription level of IL-1beta and IL-8 mRNA induced by TNF-alpha. trbp 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 17230585-5 2007 As compared to placebo fecal water, beta-glucan enriched fecal water significantly increased IL-8 production in HT29 (5.0%; p = 0.046) and INT407 cells (22.0%; p = 0.028). beta-Glucans 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 17230585-5 2007 As compared to placebo fecal water, beta-glucan enriched fecal water significantly increased IL-8 production in HT29 (5.0%; p = 0.046) and INT407 cells (22.0%; p = 0.028). Water 63-68 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 17224793-7 2007 The SA treatment also decreased cytomix-induced IL-6 and IL-8 production in a dose-dependent manner. sodium arsenite 4-6 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 16862172-8 2007 Immunoblot analysis showed that pretreatment of NHBE cells with EGCG resulted in a significant downregulation of NF-kappaB-regulated proteins cyclin D1, MMP-9, IL-8 and iNOS. epigallocatechin gallate 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 16942919-3 2007 Simvastatin treatment did not inhibit AgLDL-induced macrophage lipid accumulation, but significantly increased the secretion of IL-1beta and IL-8 from macrophages, whilst inhibiting the secretion of tumor necrosis factor-alpha (TNF-alpha) and having no significant effect on IL-6 secretion. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 17113069-4 2007 Scopoletin significantly and dose-dependently inhibits the way in which phorbol 12-myristate 13-acetate (PMA) plus A23187 induces the production of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 (P<0.05). Scopoletin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 17113069-4 2007 Scopoletin significantly and dose-dependently inhibits the way in which phorbol 12-myristate 13-acetate (PMA) plus A23187 induces the production of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 (P<0.05). Tetradecanoylphorbol Acetate 72-103 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 17113069-4 2007 Scopoletin significantly and dose-dependently inhibits the way in which phorbol 12-myristate 13-acetate (PMA) plus A23187 induces the production of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 (P<0.05). Tetradecanoylphorbol Acetate 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 17113069-4 2007 Scopoletin significantly and dose-dependently inhibits the way in which phorbol 12-myristate 13-acetate (PMA) plus A23187 induces the production of inflammatory cytokines such as tumor necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 (P<0.05). Calcimycin 115-121 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 17113069-5 2007 The maximal rates at which scopoletin (0.2 mM) inhibited the production of TNF-alpha, IL-6, and IL-8 were 41.6%+/-4.2%, 71.9%+/-2.5%, and 43.0%+/-5.7%, respectively. Scopoletin 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 16962273-0 2007 Inhibitory effect of flavonoid baicalin on degranulation of human polymorphonuclear leukocytes induced by interleukin-8: potential role in periodontal diseases. Flavonoids 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 106-119 16962273-0 2007 Inhibitory effect of flavonoid baicalin on degranulation of human polymorphonuclear leukocytes induced by interleukin-8: potential role in periodontal diseases. baicalin 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 106-119 16962273-2 2007 In the present study, we investigated whether baicalin could block polymorphonuclear leukocytes (PMNs) degranulation induced by interleukin (IL)-8, a CXC chemokine. baicalin 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 128-146 16962273-7 2007 The present study concludes that baicalin could block MMP-8 release from PMNs induced by IL-8, which suggests that it may play an important role in the prevention and treatment of periodontal disease. baicalin 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 17202379-7 2007 Surprisingly, the TLR9 ligand CpG oligodeoxynucleotide 2006 was able to specifically inhibit poly(I:C)-induced IL-8 and IDO expression. Poly I-C 93-102 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 17097222-0 2007 Sulfatide increases adiponectin and decreases TNF-alpha, IL-6, and IL-8 in human adipose tissue in vitro. Sulfoglycosphingolipids 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 17097222-7 2007 The C16:0 sulfatide has been shown to activate potassium channels in beta-cells, and glibenclamide, an ATP-sensitive K+-(KATP) channel blocker, reversed the C16:0-induced decrement in stimulated TNF-alpha, IL-6, and IL-8 release in adipocytes. Glyburide 85-98 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 17061983-0 2007 Macrolides inhibit IL17-induced IL8 and 8-isoprostane release from human airway smooth muscle cells. Macrolides 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 17097691-0 2007 Involvement of protein kinase Cdelta in iron chelator-induced IL-8 production in human intestinal epithelial cells. Iron 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 17097691-1 2007 We have shown that the bacterial iron chelator, deferoxamine (DFO), triggers inflammatory signals, including the production of CXC chemokine IL-8, in human intestinal epithelial cells (IECs) by activating ERK1/2 and p38 kinase pathways. Iron 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 17097691-1 2007 We have shown that the bacterial iron chelator, deferoxamine (DFO), triggers inflammatory signals, including the production of CXC chemokine IL-8, in human intestinal epithelial cells (IECs) by activating ERK1/2 and p38 kinase pathways. Deferoxamine 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 17097691-1 2007 We have shown that the bacterial iron chelator, deferoxamine (DFO), triggers inflammatory signals, including the production of CXC chemokine IL-8, in human intestinal epithelial cells (IECs) by activating ERK1/2 and p38 kinase pathways. Deferoxamine 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 17097691-2 2007 In the present study, we show that PKCdelta, one of the novel protein kinase C (PKC) isoforms, involves in signal transduction pathways leading to DFO-induced IL-8 production. Deferoxamine 147-150 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 17097691-3 2007 Pretreatment of human intestinal epithelial HT-29 cells with rottlerin showed remarkable inhibition of DFO-induced IL-8 production. rottlerin 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 17097691-3 2007 Pretreatment of human intestinal epithelial HT-29 cells with rottlerin showed remarkable inhibition of DFO-induced IL-8 production. Deferoxamine 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 17097691-7 2007 In addition, suppression of endogenous PKCdelta by siRNA significantly reduced DFO-induced IL-8 production. Deferoxamine 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 17097691-8 2007 Collectively, these results suggest that PKCdelta plays a pivotal role in signaling pathways leading to iron chelator-induced IL-8 production in human IECs. Iron 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 17012372-0 2007 Moxifloxacin but not ciprofloxacin or azithromycin selectively inhibits IL-8, IL-6, ERK1/2, JNK, and NF-kappaB activation in a cystic fibrosis epithelial cell line. Moxifloxacin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 17012372-2 2007 We showed that moxifloxacin (MXF) inhibits IL-8 and MAPK activation in monocytic and respiratory epithelial cells. Moxifloxacin 15-27 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 17012372-2 2007 We showed that moxifloxacin (MXF) inhibits IL-8 and MAPK activation in monocytic and respiratory epithelial cells. Moxifloxacin 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 17184586-1 2007 AIM: To examine the inhibitive effects of triptolide on the expression of IL-8, monocyte chemotactic protein (MCP)-1, and matrix metalloproteinases (MMP)-3 in subepithelial myofibroblasts (SEMF) stimulated with IL-1beta. triptolide 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16905640-9 2007 Sulforaphane pretreatment inhibited IL-8 production by BEAS-2B cells upon stimulation with diesel extract. sulforaphane 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 17061983-7 2007 IL17-induced IL8 production was decreased by both erythromycin and azithromycin. Erythromycin 50-62 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 17061983-7 2007 IL17-induced IL8 production was decreased by both erythromycin and azithromycin. Azithromycin 67-79 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 17061983-8 2007 In nonstimulated condition, IL8 production only increased at the highest dose of azithromycin. Azithromycin 81-93 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 17061983-11 2007 We conclude that macrolides (but not steroids/immunosuppressive agents) inhibit IL17-induced IL8 production in human primary airway smooth muscle cells via a reduction in MAPK activation and 8-isoprostane production. Macrolides 17-27 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 17430188-10 2007 We have found that carinosine (beta-Ala-His) suppressed the secretion of such inflammatory cytokines as IL-8 in human intestinal epithelial cells, suggesting its anti-inflammatory function in the intestines. carinosine 19-29 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 18556829-5 2007 In order to determine the possible contribution of G protein, HUVEC were pretreated with an inhibitor of G-protein activation, GDPbetaS, which abrogated the low shear stress-induced IL-8 gene expression. guanosine 5'-O-(2-thiodiphosphate) 127-135 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 18556829-8 2007 These findings therefore demonstrate the involvement of several signaling molecules, including tyrosine kinase, G protein, calcium, phospholipase C, and cAMP-dependent protein kinase, in the low shear stress-induced IL-8 gene expression. Calcium 123-130 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 16996047-0 2007 Effects of hyperbaric oxygen therapy on circulating interleukin-8, nitric oxide, and insulin-like growth factors in patients with type 2 diabetes mellitus. Oxygen 22-28 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 16574124-8 2007 DHEA at the above mention concentration also inhibited the mRNA expression of MCP-1 and IL-8 in basal conditions but not in TNF-alpha-stimulated conditions. Dehydroepiandrosterone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 17202660-2 2007 In this study, our aim was to examine the anti-inflammatory mechanism of TET through measuring the inducible nitric oxide synthase (iNOS), cyclooxygenase-1, and -2 (COX-1 and COX-2) expression, cytokines (TNF-alpha, IL-4 and IL-8) formation, nitric oxide (NO) release and prostaglandin E2 (PGE2) generation in lipopolysaccharide (LPS)-induced human monocytic (THP-1) cells. tetrandrine 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 18997280-5 2007 Here, we report that after differentiating THP-1 cells to macrophages, ritonavir treatment (10 microg/mL) significantly increases expression of proinflammatory cytokines, IL-6, MCP-1 and IL-8, at both mRNA and protein levels. Ritonavir 71-80 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 17243915-4 2007 The aim of this study was to investigate whether plasma concentrations of interleukin-6, interleukin-8, C-reactive protein, and monocyte chemoattractant protein-1 are increased with higher plasma homocysteine concentrations and whether decreasing homocysteine by vitamin supplementation decreases the concentration of these markers. Homocysteine 196-208 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 17243915-6 2007 RESULTS: At baseline, plasma homocysteine concentration was weakly associated with interleukin-8, but not with interleukin-6, C-reactive protein or monocyte chemoattractant protein-1. Homocysteine 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 17243915-8 2007 CONCLUSIONS: At baseline homocysteine was only weakly correlated with interleukin-8, but not with interleukin-6, C-reactive protein or monocyte chemoattractant protein-1. Homocysteine 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 17093102-0 2007 Binding of glucuronoxylomannan to the CD14 receptor in human A549 alveolar cells induces interleukin-8 production. glucuronoxylomannan 11-30 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 17093102-3 2007 In the current study, we demonstrate that GXM binds to the CD14 receptor in human type II alveolar epithelial cells, resulting in the production of the proinflammatory chemokine interleukin-8. glucuronoxylomannan 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 178-191 17430188-10 2007 We have found that carinosine (beta-Ala-His) suppressed the secretion of such inflammatory cytokines as IL-8 in human intestinal epithelial cells, suggesting its anti-inflammatory function in the intestines. 2-(3-azaniumylpropanoylamino)-3-(1H-imidazol-5-yl)propanoate 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 17160716-0 2007 Phytic acid modulates in vitro IL-8 and IL-6 release from colonic epithelial cells stimulated with LPS and IL-1beta. Phytic Acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 17391980-0 2007 Cadmium induces interleukin-8 production via NF-kappaB activation in the human intestinal epithelial cell, Caco-2. Cadmium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 17391980-5 2007 The results of this assay demonstrated that the transcriptional activity of IL-8 was increased by CdCl2. Cadmium Chloride 98-103 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 17391980-7 2007 Site-directed mutation of the NF-kappaB consensus element in the human IL-8 promoter abolished the increased transcriptional activity by CdCl2. Cadmium Chloride 137-142 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 17391980-10 2007 Our results suggest that CdCl2 induced IL-8 secretion, its transcription, and its transcriptional activation regulated by NF-kappaB via I-kappaB alpha degradation. Cadmium Chloride 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 17410895-0 2007 Effect of acetic NaF solutions on fluoride-containing dental restorative materials. Fluorides 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 17410895-1 2007 The aim of this study was to evaluate the effect of acetic NaF solutions on fluoride-containing restorative materials. Fluorides 76-84 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 17160716-2 2007 The aim of this study was to examine the role of PA in immunologic function of intestinal epithelial cells by analyzing its effect on interleukin (IL)-8 and IL-6 secretion by colonocytes and its role in the response of these cells to bacterial lipopolysaccharides (LPS) and IL-1beta. Phytic Acid 49-51 C-X-C motif chemokine ligand 8 Homo sapiens 134-152 17160716-5 2007 PA had a suppressive effect on IL-8 basal release and it dose dependently reduced IL-8 secretion by colonocytes stimulated with LPS and IL-1beta. Phytic Acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 17160716-5 2007 PA had a suppressive effect on IL-8 basal release and it dose dependently reduced IL-8 secretion by colonocytes stimulated with LPS and IL-1beta. Phytic Acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 17160716-8 2007 The ability of PA to modulate IL-8 and IL-6 release suggests that PA present in the intestinal milieu may exert immunoregulatory effects on colonic epithelium under physiological conditions or during microbe-induced infection/inflammation in order to maintain the colonic mucosa in a noninflammatory state or to counteract infection. Phytic Acid 15-17 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 17160716-8 2007 The ability of PA to modulate IL-8 and IL-6 release suggests that PA present in the intestinal milieu may exert immunoregulatory effects on colonic epithelium under physiological conditions or during microbe-induced infection/inflammation in order to maintain the colonic mucosa in a noninflammatory state or to counteract infection. Phytic Acid 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 17030560-2 2007 Interleukin-8 belongs to a subfamily of CXC chemokines containing a Glu-Leu-Arg (ELR) motif. Glu-Leu-Arg 68-79 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 17050564-8 2007 There were significant decreases in plasma IL-4, IL-8 and eotaxin levels after 3 weeks of treatment with clarithromycin. Clarithromycin 105-119 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 17849273-0 2007 Effect of hydrogen peroxide on interleukin-8 synthesis and death of Caco-2 cells. Hydrogen Peroxide 10-27 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 16709662-5 2007 The major CLPF-activating and IL8 inducing protein was purified using fast-performance liquid chromatography (HiPrep 16/60 Sephacryl S-200 High Resolution Column) and sodium dodecyl sulphate gel electrophoresis. sephacryl s 123-134 C-X-C motif chemokine ligand 8 Homo sapiens 10-33 16709662-5 2007 The major CLPF-activating and IL8 inducing protein was purified using fast-performance liquid chromatography (HiPrep 16/60 Sephacryl S-200 High Resolution Column) and sodium dodecyl sulphate gel electrophoresis. Sodium Dodecyl Sulfate 167-190 C-X-C motif chemokine ligand 8 Homo sapiens 10-33 17849273-3 2007 We investigated the time- and dose-dependent induction of IL-8 by hydrogen peroxide in the human colon adenocarcinoma cell line Caco-2. Hydrogen Peroxide 66-83 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 17849273-8 2007 In nonfilter-grown Caco-2 cells, 1 mM of hydrogen peroxide induced the highest level of IL-8 production 24 hr after treatment. Hydrogen Peroxide 41-58 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 17849273-9 2007 In filter-grown Caco-2 cells, IL-8 was produced only on the apical side in response to 1 mM of hydrogen peroxide. Hydrogen Peroxide 95-112 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 17135765-0 2007 Epigallocatechin-3-gallate inhibits secretion of TNF-alpha, IL-6 and IL-8 through the attenuation of ERK and NF-kappaB in HMC-1 cells. epigallocatechin gallate 0-26 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 17849273-11 2007 In filter-grown Caco-2 cells 10 mM hydrogen peroxide induced the highest IL-8 level on the apical as well as basolateral side. Hydrogen Peroxide 35-52 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 17135765-2 2007 In the present study, we investigated the effect of EGCG on the secretion of TNF-alpha, IL-6 and IL-8, as well as its possible mechanism of action by using the human mast cell line (HMC-1). epigallocatechin gallate 52-56 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 17541275-7 2007 On the contrary, only IL-8 induced the TBM of neutrophils. metsulfuron methyl 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 17135765-5 2007 RESULTS: EGCG (100 microM) inhibited PMA+A23187-induced TNF-alpha, IL-6 and IL-8 expression and production. epigallocatechin gallate 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 17135765-5 2007 RESULTS: EGCG (100 microM) inhibited PMA+A23187-induced TNF-alpha, IL-6 and IL-8 expression and production. Calcimycin 41-47 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 17135765-8 2007 CONCLUSION: EGCG inhibited the production of TNF-alpha, IL-6 and IL-8 through the inhibition of the intracellular Ca(2+) level, and of ERK1/2 and NF-kappaB activation. epigallocatechin gallate 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 17448722-5 2007 In parallel, a short-term (2h) cell exposure to AAT/LPS significantly enhances LPS-induced NF kappaB (p50 and p65) activation in conjunction with increased TNFalpha, IL-1 beta and IL-8 release. Deuterium 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 17541276-9 2007 RESULTS: As previously reported, IL-8-stimulated neutrophils significantly augmented the TBM of eosinophils. metsulfuron methyl 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 17541276-12 2007 Finally, theophylline attenuated the superoxide anion generation from IL-8-stimulated neutrophils on the Matrigel-coated plates. Superoxides 37-53 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17541276-12 2007 Finally, theophylline attenuated the superoxide anion generation from IL-8-stimulated neutrophils on the Matrigel-coated plates. Theophylline 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17541283-7 2007 Preincubation with 100 microM chloroquine significantly inhibited the expression of mRNA for RANTES, IP-10, and IL-8, stimulated by poly I:C, indicating that poly I:C may react with a receptor expressed inside the cells. Chloroquine 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 17621557-6 2007 When added to human macrophage culture, rFC blocks the LPS-induced phosphorylation of p38, which, in turn, inhibits the consequential overexpression of TNF-alpha and IL-8. lps 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 17886062-10 2007 BaP and Phe significantly enhanced cytokine secretion (IL-4, IL-8) and histamine release from purified basophils without antigen added, and secretion was not further enhanced by rBet v 1 stimulation. Benzo(a)pyrene 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 17886062-10 2007 BaP and Phe significantly enhanced cytokine secretion (IL-4, IL-8) and histamine release from purified basophils without antigen added, and secretion was not further enhanced by rBet v 1 stimulation. phenanthrene 8-11 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 17621556-3 2007 Here, we report that, at concentrations that did not induce whole blood cytokine production when tested separately, (1-->3)-beta-D-glucans powerfully co-stimulated cytokine production (IL-6/IL-8) induced by ligands for TLR1/2, TLR2/6, TLR4, and TLR5. beta-D-Glucan 127-141 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 17008886-8 2007 Nicotine significantly decreased IL-8 and -6 release by HMEC-1 maintained in both patients" and controls" sera, but only IL-6 release by keratinocytes maintained in patients" sera. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 33-44 17008886-11 2007 The phytoestrogen biochanin A alone and in combination with nicotine further decreased the secretion of IL-8, -6, and VEGF in all experimental settings. Nicotine 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 17909718-8 2007 RESULTS: Postoperative plasma concentrations of IL-6 (days 1 and 2), IL-8 (days 2 and 3), and CRP (days 1-4) were significantly lower in the steroid than in the control group. Steroids 141-148 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 16902417-7 2007 Only carboxylic acid-coated QDs significantly increased release of IL-1beta, IL-6, and IL-8. Carboxylic Acids 5-20 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 17895603-7 2007 Furthermore, a mAb to the beta-glucan receptor, Dectin-1, significantly (P<0.05) blocked the Sophy beta-glucan induced DNA synthesis in the PBMCs, and Sophy beta-glucan-induced production of IL-8 in the U937 cells. beta-Glucans 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 18260853-10 2007 At the background of therapy with simvastatin we noted significant lowering of proinflammatory cytokines (TNFalpha, IL-1beta, IL-6, IL-8) in blood serum irrespective of level of low density lipoprotein cholesterol, betterment of functional state of the left ventricle, positive clinical dynamics of CHF. Simvastatin 34-45 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 17135982-0 2007 Pneumococcal peptidoglycan-polysaccharides induce the expression of interleukin-8 in airway epithelial cells by way of nuclear factor-kappaB, nuclear factor interleukin-6, or activation protein-1 dependent mechanisms. pneumococcal peptidoglycan-polysaccharides 0-42 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 17135982-4 2007 However, the PGPS-induced IL-8 promoter activation in rodent middle ear epithelial cells required NF-kappaB and NF-IL6 but not AP-1. pgps 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 17084411-12 2007 IL-6 levels were highest in patients with TRAM operations, being the most extensive procedure studied, whereas the highest IL-8 levels were seen in women with a saline filled silicone implant suggesting immunomodulation by foreign material. Silicones 175-183 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 17551258-5 2007 Exogenous ADMA (30 microM) also increased ROS generation and the levels of TNF-alpha and IL-8, decreased the levels of nitrite/nitrate, upregulated CXCR2 gene expression, increased endothelial cell binding with monocytes and activated the NF-kappaB pathway, which was inhibited by pretreatment with losartan or L-arginine. N,N-dimethylarginine 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 17710245-0 2007 Curcumin (1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione) blocks the chemotaxis of neutrophils by inhibiting signal transduction through IL-8 receptors. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 17710245-0 2007 Curcumin (1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione) blocks the chemotaxis of neutrophils by inhibiting signal transduction through IL-8 receptors. 1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione 10-69 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 17710245-2 2007 Chemotactic activity via human recombinant IL-8 (hrIL-8) was significantly inhibited by curcumin. Curcumin 88-96 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 17710245-3 2007 Curcumin reduced calcium ion flow induced by internalization of the IL-8 receptor. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 17710245-3 2007 Curcumin reduced calcium ion flow induced by internalization of the IL-8 receptor. Calcium 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 17710245-4 2007 We analyzed flow cytometry to evaluate the status of the IL-8 receptor after curcumin treatment. Curcumin 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 17710245-7 2007 Following curcumin treatment, immunoprecipitation studies showed that the IL-8 receptor was associated with larger amounts of active Rab11 than that in control cells. Curcumin 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 17710245-9 2007 The mechanism for antiinflammatory response by curcumin may involve unique regulation of the Rab11 trafficking molecule in recycling of IL-8 receptors. Curcumin 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 17895603-8 2007 The Sophy beta-glucan-induced production of IL-8 in the U937 cells was significantly (P<0.01) blocked by the conventional protein kinase C (PKC) inhibitor Go6976, the novel PKC inhibitor Rottlerin, the protein kinase A (PKA) inhibitor H-89, and the protein tyrosine kinase (PTK) inhibitor herbimycin A. beta-Glucans 10-21 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17895603-8 2007 The Sophy beta-glucan-induced production of IL-8 in the U937 cells was significantly (P<0.01) blocked by the conventional protein kinase C (PKC) inhibitor Go6976, the novel PKC inhibitor Rottlerin, the protein kinase A (PKA) inhibitor H-89, and the protein tyrosine kinase (PTK) inhibitor herbimycin A. Go 6976 158-164 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17895603-8 2007 The Sophy beta-glucan-induced production of IL-8 in the U937 cells was significantly (P<0.01) blocked by the conventional protein kinase C (PKC) inhibitor Go6976, the novel PKC inhibitor Rottlerin, the protein kinase A (PKA) inhibitor H-89, and the protein tyrosine kinase (PTK) inhibitor herbimycin A. rottlerin 190-199 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17895603-8 2007 The Sophy beta-glucan-induced production of IL-8 in the U937 cells was significantly (P<0.01) blocked by the conventional protein kinase C (PKC) inhibitor Go6976, the novel PKC inhibitor Rottlerin, the protein kinase A (PKA) inhibitor H-89, and the protein tyrosine kinase (PTK) inhibitor herbimycin A. N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide 238-242 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17895603-8 2007 The Sophy beta-glucan-induced production of IL-8 in the U937 cells was significantly (P<0.01) blocked by the conventional protein kinase C (PKC) inhibitor Go6976, the novel PKC inhibitor Rottlerin, the protein kinase A (PKA) inhibitor H-89, and the protein tyrosine kinase (PTK) inhibitor herbimycin A. herbimycin 292-304 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 17895603-10 2007 Studies employing reverse transcriptase-polymerase chain reaction (RT-PCR) showed that Sophy beta-glucan stimulated the expression of IL-8 mRNA in the U937 cells, and that this induction was inhibited by Rottlerin. beta-Glucans 93-104 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 17895603-10 2007 Studies employing reverse transcriptase-polymerase chain reaction (RT-PCR) showed that Sophy beta-glucan stimulated the expression of IL-8 mRNA in the U937 cells, and that this induction was inhibited by Rottlerin. rottlerin 204-213 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 17389814-8 2007 Equimolar doses of exogenous IL-10 or DEX produced up to 83% inhibition of IL-8 from PMNs. Dexamethasone 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 17344653-8 2007 In the presence of 20 mM vitamin C, even a stronger stimulatory effect was noted for the percentage of IL-8 (e.g., 46.7% increase, p < 0.001) and TNF-alpha producing neonatal monocytes (e.g., 69.2% increase, p = 0.004; n = 20). Ascorbic Acid 25-34 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 17389814-9 2007 Exogenous IL-10 was more potent than DEX, on an equimolar basis, with regard to IL-8 release from PBMCs (90 vs. 33% respectively at a 10 nanomolar level). Dexamethasone 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 17344660-6 2007 RESULTS: IL-8 mRNA levels were significantly increased in whole blood both during PA and PI, while MCP-1 mRNA levels were not. Protactinium 82-84 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 17344663-0 2007 Perfluorocarbon suppresses lipopolysaccharide- and alpha-toxin-induced interleukin-8 release from alveolar epithelial cells. Fluorocarbons 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 17079162-4 2007 Fisetin decreased phorbol-12-myristate 13-acetate plus calcium ionophore A23187 (PMACI)-stimulated gene expression and production of tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-1beta, IL-4, IL-6, and IL-8 in HMC-1 cells. fisetin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 17079162-4 2007 Fisetin decreased phorbol-12-myristate 13-acetate plus calcium ionophore A23187 (PMACI)-stimulated gene expression and production of tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-1beta, IL-4, IL-6, and IL-8 in HMC-1 cells. Tetradecanoylphorbol Acetate 18-49 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 17079162-4 2007 Fisetin decreased phorbol-12-myristate 13-acetate plus calcium ionophore A23187 (PMACI)-stimulated gene expression and production of tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-1beta, IL-4, IL-6, and IL-8 in HMC-1 cells. Calcimycin 73-79 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 17079162-4 2007 Fisetin decreased phorbol-12-myristate 13-acetate plus calcium ionophore A23187 (PMACI)-stimulated gene expression and production of tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-1beta, IL-4, IL-6, and IL-8 in HMC-1 cells. pmaci 81-86 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 16413994-7 2007 RESULTS: Forced vital capacity was increased and sputum IL-8 levels decreased after 4 weeks of theophylline treatment. Theophylline 95-107 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 16413994-9 2007 Levels of IL-8 and TNF-alpha released by LPS-stimulated THP-1 cells were reduced by treatment with theophylline at 10microg/ml. Theophylline 99-111 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 16413994-0 2007 Long-term treatment with theophylline reduces neutrophils, interleukin-8 and tumor necrosis factor-alpha in the sputum of patients with chronic obstructive pulmonary disease. Theophylline 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 59-104 16413994-10 2007 In contrast, IL-8 levels released by LPS-stimulated neutrophils were reduced by treatment with theophylline at 100microg/ml. Theophylline 95-107 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 16530440-1 2007 Anti-inflammatory effect of desloratadine (DL), including, but not limited to depression of production of IL-4, IL-6 and IL-8, has been shown in several in vitro experiments but only a few in vivo studies refer to this findings. desloratadine 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 16530440-1 2007 Anti-inflammatory effect of desloratadine (DL), including, but not limited to depression of production of IL-4, IL-6 and IL-8, has been shown in several in vitro experiments but only a few in vivo studies refer to this findings. desloratadine 43-45 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 17172977-7 2007 The addition of NaCl lowered the production of IL-8, TNF-alpha, and IL-1 receptor antagonist by neutrophils, and IL-8 and IL-1beta by mononuclear cells stimulated with LPS. Sodium Chloride 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 17268170-6 2007 This IL-8 release was abolished by treatment with intracellular Ca(2+) chelator (BAPTA-AM), but not by EGTA or nifedipine. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 17268170-7 2007 Calmodulin inhibitor (calmidazolium) and tyrosine kinase inhibitor (genistein) almost completely blocked IL-8 release by HDM. calmidazolium 22-35 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 17268170-7 2007 Calmodulin inhibitor (calmidazolium) and tyrosine kinase inhibitor (genistein) almost completely blocked IL-8 release by HDM. Genistein 68-77 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 17268170-8 2007 PD98,059, an ERK pathway inhibitor, completely abolished HDM-induced IL-8 release. pd98,059 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 17202889-9 2007 CONCLUSION: TNF-alpha and IL-8 stimulation up-regulated the FAK expression of human nucleus pulposus cells, and the coadministration of dexamethasone attenuated it. Dexamethasone 136-149 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 17172977-7 2007 The addition of NaCl lowered the production of IL-8, TNF-alpha, and IL-1 receptor antagonist by neutrophils, and IL-8 and IL-1beta by mononuclear cells stimulated with LPS. Sodium Chloride 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 17165981-7 2006 The best photoactive films were obtained from poly(ethylene glycol) (PEG 400) containing NH4F for TiO2 and from aqueous NaF for WO3. wo3 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 16682428-9 2006 RESULTS: A positive correlation was identified between MCS grade, histological grade (p = 0.001) and mucosal IL8 activity (p<0.001). mcs 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 17384268-5 2006 IL-8 and caspase-3 activation were both influenced by paxilline, an inhibitor of calcium-activated potassium channels. paxilline 54-63 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 17045242-3 2006 AZM reduced about 40% of IL-8 mRNA and protein expression (n=9, p=0.02, and n=4, p=0.00011) in CF cells reaching the levels of non-CF cells. Azithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 16937109-8 2006 Fluoride plaque concentrations evaluated in 12 individuals after (1) application of the active gel, (2) rinsing with 0.2% NaF, and (3) rinsing with water showed significantly higher values after rinsing with the NaF solution. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 122-125 16937109-8 2006 Fluoride plaque concentrations evaluated in 12 individuals after (1) application of the active gel, (2) rinsing with 0.2% NaF, and (3) rinsing with water showed significantly higher values after rinsing with the NaF solution. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 212-215 17078003-0 2006 Involvement of cyclooxygenase-2--prostaglandin E2 pathway in interleukin-8 production in gastric cancer cells. Dinoprostone 33-49 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 17078003-2 2006 The effect of PGE(2) on the proinflammatory chemokine interleukin-8 (IL-8) in the gastric epithelial cells has not been defined yet. Prostaglandins E 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 17078003-2 2006 The effect of PGE(2) on the proinflammatory chemokine interleukin-8 (IL-8) in the gastric epithelial cells has not been defined yet. Prostaglandins E 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 16300955-7 2006 Recently we reported on the radioiodination of interleukin-8 (IL-8) using the pyridine carboxylate-derived activated ester. pyridine carboxylate-derived activated ester 78-122 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 16300955-7 2006 Recently we reported on the radioiodination of interleukin-8 (IL-8) using the pyridine carboxylate-derived activated ester. pyridine carboxylate-derived activated ester 78-122 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 16628233-3 2006 Treatment of HeLa cells with apicidin increases transcriptional activity of NF-kappaB and its target gene IL-8 and cIAP-1 induction, which involves the activation of IKK-IkappaBalpha signaling pathway through Sp1-dependent de novo protein synthesis. apicidin 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 16628233-4 2006 In parallel, apicidin treatment leads to histone hyperacetylation in the IL-8 promoter region independent of NF-kappaB signaling pathway, which is not sufficient for full transcription of IL-8 gene. apicidin 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 17078003-12 2006 PGE(2)-induced IL-8 production was inhibited by pretreatment with EP2 and EP4 antagonists. Dinoprostone 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 17078003-14 2006 The amount of IL-8 antigen increased slightly, but not significantly, with arachidonic acid treatment. Arachidonic Acid 75-91 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 17078003-16 2006 These results suggest that the COX-2-PGE(2) pathway may be involved in IL-8 production in gastric epithelial cells. Prostaglandins E 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 16682428-12 2006 CONCLUSION: MCS grading is associated with the degree of histological inflammation and mucosal IL8 activity in patients with quiescent ulcerative colitis, and may predict the probability of subsequent disease relapse in patients with ulcerative colitis in remission. mcs 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 17269555-5 2006 DHA and CLA significantly decreased the production of IL-8 in response to stimulation by TNF-alpha [2907 +/- 970 (DHA) and 6471 +/- 1203 (CLA) vs. 12,287 +/- 2309 (control) pg/mL; P < or = 0.05, mean +/- SEM], whereas both EPA and DHA reduced histamine-stimulated RANTES (regulation on activation, T cell-expressed and -secreted) production [2314 +/- 861 (EPA) and 877 +/- 326 (DHA) vs. 8526 +/- 1118 (control) pg/mL; P < or = 0.03]. dehydroacetic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 17082725-6 2006 In comparison with cells from controls, PMNs obtained from patients before starting simvastatin treatment showed higher resting and fMLP-stimulated IL-8 release (P = 0.007 and P = 0.002, respectively) and ROS generation (resting, P = 0.009; and fMLP-stimulated, P = 0.046), whereas migration and the chemotactic index did not significantly differ. Simvastatin 84-95 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 17269555-5 2006 DHA and CLA significantly decreased the production of IL-8 in response to stimulation by TNF-alpha [2907 +/- 970 (DHA) and 6471 +/- 1203 (CLA) vs. 12,287 +/- 2309 (control) pg/mL; P < or = 0.05, mean +/- SEM], whereas both EPA and DHA reduced histamine-stimulated RANTES (regulation on activation, T cell-expressed and -secreted) production [2314 +/- 861 (EPA) and 877 +/- 326 (DHA) vs. 8526 +/- 1118 (control) pg/mL; P < or = 0.03]. dehydroacetic acid 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 16988013-2 2006 In A549 pulmonary cells, dexamethasone and the prototypical dissociated ligand RU24858 (Mol Endocrinol 11:1245-1255, 1997) repress interleukin (IL)-1beta-induced expression of cyclooxygenase (COX)-2 and IL-8. Dexamethasone 25-38 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 17269555-5 2006 DHA and CLA significantly decreased the production of IL-8 in response to stimulation by TNF-alpha [2907 +/- 970 (DHA) and 6471 +/- 1203 (CLA) vs. 12,287 +/- 2309 (control) pg/mL; P < or = 0.05, mean +/- SEM], whereas both EPA and DHA reduced histamine-stimulated RANTES (regulation on activation, T cell-expressed and -secreted) production [2314 +/- 861 (EPA) and 877 +/- 326 (DHA) vs. 8526 +/- 1118 (control) pg/mL; P < or = 0.03]. dehydroacetic acid 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 17269555-5 2006 DHA and CLA significantly decreased the production of IL-8 in response to stimulation by TNF-alpha [2907 +/- 970 (DHA) and 6471 +/- 1203 (CLA) vs. 12,287 +/- 2309 (control) pg/mL; P < or = 0.05, mean +/- SEM], whereas both EPA and DHA reduced histamine-stimulated RANTES (regulation on activation, T cell-expressed and -secreted) production [2314 +/- 861 (EPA) and 877 +/- 326 (DHA) vs. 8526 +/- 1118 (control) pg/mL; P < or = 0.03]. Histamine 246-255 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 17269555-5 2006 DHA and CLA significantly decreased the production of IL-8 in response to stimulation by TNF-alpha [2907 +/- 970 (DHA) and 6471 +/- 1203 (CLA) vs. 12,287 +/- 2309 (control) pg/mL; P < or = 0.05, mean +/- SEM], whereas both EPA and DHA reduced histamine-stimulated RANTES (regulation on activation, T cell-expressed and -secreted) production [2314 +/- 861 (EPA) and 877 +/- 326 (DHA) vs. 8526 +/- 1118 (control) pg/mL; P < or = 0.03]. dehydroacetic acid 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 16988013-2 2006 In A549 pulmonary cells, dexamethasone and the prototypical dissociated ligand RU24858 (Mol Endocrinol 11:1245-1255, 1997) repress interleukin (IL)-1beta-induced expression of cyclooxygenase (COX)-2 and IL-8. RU24858 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 16988013-6 2006 Analysis of IL-1beta-induced steady-state mRNA levels for IL-8 and COX-2 show that dexamethasone- and RU24858-dependent repression of these genes is attenuated by inhibitors of transcription and protein synthesis. Dexamethasone 83-96 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 17172406-3 2006 Bortezomib synergized with IFN-alpha to promote apoptosis via a tumor necrosis factor-related apoptosis-inducing ligand-associated mechanism but did not inhibit production of proangiogenic factors (vascular endothelial growth factor, basic fibroblast growth factor, and interleukin-8) in human UM-UC-5 cells. Bortezomib 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 270-283 17083726-9 2006 High sputum IL-8 and IL-17A mRNA levels were also found in moderate-to-severe (persistent) asthmatics on inhaled steroid treatment. Steroids 113-120 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 17089061-12 2006 DSS induced the weak release of IL-8, IL-6, and TGF-beta1. Dextran Sulfate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 17082639-0 2006 A novel role of hypoxia-inducible factor in cobalt chloride- and hypoxia-mediated expression of IL-8 chemokine in human endothelial cells. cobaltous chloride 44-59 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 17082639-3 2006 In this study, we used human pulmonary microvascular endothelial cells and human dermal microvascular endothelial immortalized cell line to delineate the cellular signaling mechanism of hypoxia- and CoCl2 (a mimetic of hypoxia)-induced IL-8 expression, and the latter"s role in chemotaxis of polmorphonuclear neutrophils. cobaltous chloride 199-204 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 17082639-4 2006 We show that hypoxia- and CoCl2-induced IL-8 mRNA and protein expression involved activation of PI3K/Akt and p38 MAPK, but not MEK kinase. cobaltous chloride 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 17082639-5 2006 Analysis of some transcription factors associated with IL-8 promoter revealed that hypoxia and CoCl2 increased DNA-binding activity of hypoxia-inducible factor-1alpha (HIF-1alpha), NF-kappaB, and AP-1. cobaltous chloride 95-100 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 16997914-7 2006 Disruption of Hx8 by deletion or mutation distorts an H-bonding network, involving highly conserved amino acids within TM2, TM7, and Hx8, that is crucial for positioning of the TM domains, coupling to Galphaq, and CXCL8 binding. galphaq 201-208 C-X-C motif chemokine ligand 8 Homo sapiens 214-219 16822944-4 2006 The aim of this study was to determine whether human ASMC (HASMC) express functional IL-8 receptors (CXCR1 and CXCR2) linked to cell contraction and migration. asmc 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 16794257-3 2006 Pretreatment with quercetin and the PI 3-kinase inhibitor LY294002 each reduced TNF-alpha-induced IL-8 and monocyte chemoattractant protein (MCP)-1 (also called CCL2) expression in cultured human airway epithelial cells. Quercetin 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 16794257-3 2006 Pretreatment with quercetin and the PI 3-kinase inhibitor LY294002 each reduced TNF-alpha-induced IL-8 and monocyte chemoattractant protein (MCP)-1 (also called CCL2) expression in cultured human airway epithelial cells. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 16822944-4 2006 The aim of this study was to determine whether human ASMC (HASMC) express functional IL-8 receptors (CXCR1 and CXCR2) linked to cell contraction and migration. hasmc 59-64 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 16822944-9 2006 IL-8 also contracted the HASMC, decreasing the length of cells by 15%, and induced a 2.5-fold increase in migration. hasmc 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16979119-6 2006 Clinically relevant concentrations of fenretinide (1.25, 2.5 and 5 microM) inhibited TNF-alpha-induced IL-8 production of CF cells by up to 73% but had no effect or increased the IL-8 production in non-CF cells. Fenretinide 38-49 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 16947006-5 2006 NaF was used to leach the Al(3+) ion from the MIP. ALUMINUM ION 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 16931790-5 2006 Using the UPR inducing agent tunicamycin and selective siRNA targeting of the ATF4 and XBP1 branches of the UPR, we demonstrate that these transcription factors are essential mediators of IL8, IL6, and MCP1 expression in human aortic ECs required for maximal inflammatory gene expression in the basal state and after oxPAPC treatment. Tunicamycin 29-40 C-X-C motif chemokine ligand 8 Homo sapiens 188-191 16931790-5 2006 Using the UPR inducing agent tunicamycin and selective siRNA targeting of the ATF4 and XBP1 branches of the UPR, we demonstrate that these transcription factors are essential mediators of IL8, IL6, and MCP1 expression in human aortic ECs required for maximal inflammatory gene expression in the basal state and after oxPAPC treatment. oxpapc 317-323 C-X-C motif chemokine ligand 8 Homo sapiens 188-191 17077523-6 2006 We showed that GJWGM inhibited the production of tumor necrosis factor (TNF)-alpha, interleukin (IL)-1alpha, IL-6, and IL-8 induced by LPS in dose dependent manner (p<0.05). gjwgm 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 16849637-9 2006 Treatment of control neutrophils with cytokines and lipopolysaccharide (LPS) to mimic endogenous septic environment inhibited actin polymerization and tyrosine phosphorylation in response to IL-8 or LTB4. Tyrosine 151-159 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 16979119-0 2006 Inhibition of IL-8 release from CFTR-deficient lung epithelial cells following pre-treatment with fenretinide. Fenretinide 98-109 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16979119-7 2006 Although fenretinide treatment was associated with a higher intracellular ceramide content in the mutant DeltaF508 CFTR cells, the fenretinide-mediated decrease in IL-8 secretion was not consistently explained by changes in the intracellular content of this sphingolipid. Fenretinide 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 17122965-2 2006 In this study, we investigated the anti-inflammatory actions beyond the suppression of acid secretion by proton pump inhibitors (PPI), such as omeprazole and lansoprazole, on IL-8 production by gastric epithelial cells (MKN45) and human umbilical vein endothelial cells (HUVEC) and on the transendothelial migration of polymorphonuclear neutrophils (PMN). Omeprazole 143-153 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 16979119-9 2006 The fenretinide mediated decrease in IL-8 release in CF cells under TNF-alpha stimulated conditions presents the possibility that the lung inflammation in CF could be attenuated via low dose fenretinide treatment. Fenretinide 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 17122965-2 2006 In this study, we investigated the anti-inflammatory actions beyond the suppression of acid secretion by proton pump inhibitors (PPI), such as omeprazole and lansoprazole, on IL-8 production by gastric epithelial cells (MKN45) and human umbilical vein endothelial cells (HUVEC) and on the transendothelial migration of polymorphonuclear neutrophils (PMN). Lansoprazole 158-170 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 17203778-1 2006 Whether or not water pressure enhances the cytotoxic activity of sodium fluoride (NaF) against human periodontal ligament fibroblast (HPLF) was investigated. Sodium Fluoride 65-80 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 17203778-2 2006 Loading with water pressure (up to 5 g) alone did not affect the cell proliferation, but significantly enhanced the cytotoxic activity of millimolar concentrations of NaF. Water 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 17203778-4 2006 However, the enhancement of cytotoxicity of NaF under water pressure was observed even in the Ca2+ -free medium. Water 54-59 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 16979119-9 2006 The fenretinide mediated decrease in IL-8 release in CF cells under TNF-alpha stimulated conditions presents the possibility that the lung inflammation in CF could be attenuated via low dose fenretinide treatment. Fenretinide 191-202 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 17063122-6 2006 After activation with polyinosinic-polycytidylic acid, BDCs expressed higher levels of major histocompatibility complex class I, CD40, CD80, and CD83, and secreted higher levels of tumor necrosis factor-alpha, interleukin (IL)-1beta, IL-6, and IL-8 compared with MoDCs. Poly I-C 22-53 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 16795034-0 2006 Lysophospholipids increase IL-8 and MCP-1 expressions in human umbilical cord vein endothelial cells through an IL-1-dependent mechanism. Lysophospholipids 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 16965524-8 2006 IL-1alpha, IL-1beta and IL-8, but not IL-6, were detected in GCF of CsA-treated patients, but none of them was significantly associated with gingival overgrowth. Cyclosporine 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 17063122-6 2006 After activation with polyinosinic-polycytidylic acid, BDCs expressed higher levels of major histocompatibility complex class I, CD40, CD80, and CD83, and secreted higher levels of tumor necrosis factor-alpha, interleukin (IL)-1beta, IL-6, and IL-8 compared with MoDCs. tert-butyldimethylsilyl chloride 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 16890260-8 2006 Furthermore, AEMD attenuated the phorbol 12-myristate 13-acetate (PMA) and calcium ionophore A23187-stimulated TNF-alpha, IL-8 and IL-6 secretion in human mast cells. Tetradecanoylphorbol Acetate 33-64 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 17086464-5 2006 The preadministration of TJ-41 significantly inhibited increases in the serum level of keratinocyte chemoattractant (KC), which is a murine chemotaxin for neutrophils that corresponds to human interleukin-8, with respect to its concentration at 24 h after LPS challenge. tj-41 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 193-206 16890260-8 2006 Furthermore, AEMD attenuated the phorbol 12-myristate 13-acetate (PMA) and calcium ionophore A23187-stimulated TNF-alpha, IL-8 and IL-6 secretion in human mast cells. Calcium 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 16890260-8 2006 Furthermore, AEMD attenuated the phorbol 12-myristate 13-acetate (PMA) and calcium ionophore A23187-stimulated TNF-alpha, IL-8 and IL-6 secretion in human mast cells. Calcimycin 93-99 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 16919250-9 2006 We conclude that human NT2-N neurons release IL-8 and MCP-1 during 21 h of reoxygenation after 3 h of hypoxia. nt2-n 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 17047652-11 2006 Moxifloxacin completely blocked the enhanced release of IL-8 induced by 0.5 and 1 microg ml(-1) VP-16, and decreased IL-8 release from cells incubated for 72 h with 3 microg ml(-1) VP-16 (P<0.001). Moxifloxacin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 17047652-11 2006 Moxifloxacin completely blocked the enhanced release of IL-8 induced by 0.5 and 1 microg ml(-1) VP-16, and decreased IL-8 release from cells incubated for 72 h with 3 microg ml(-1) VP-16 (P<0.001). Moxifloxacin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 16963169-0 2006 Mechanisms of silica-induced IL-8 release from A549 cells: initial kinase-activation does not require EGFR activation or particle uptake. Silicon Dioxide 14-20 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 16806458-3 2006 Results indicate that a number of the primary carbon/resin materials demonstrate efficient adsorption of the cytokines studied here (TNF, IL-6 and IL-8), comparable to other adsorbents under clinical investigation. Resins, Plant 53-58 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 16963169-8 2006 The EGFR inhibitor AG1478 attenuated both silica-induced IL-8 release and phosphorylation of SFKs and ERK1/2. RTKI cpd 19-25 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 16963169-8 2006 The EGFR inhibitor AG1478 attenuated both silica-induced IL-8 release and phosphorylation of SFKs and ERK1/2. Silicon Dioxide 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 17093399-3 2006 RESULTS: Vitreous and serum concentrations of IL-8, VEGF, and ANG determined by CBA showed a strong correlation with those measured by ELISA. cba 80-83 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 17093399-7 2006 Measurements obtained by ELISA and CBA technologies were highly correlated for IL-8, VEGF, and ANG in both vitreous and serum samples. cba 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 17093399-11 2006 CBA technology is a new, accurate method to measure IL-8, VEGF, and ANG in the vitreous. cba 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 16678783-5 2006 The stimulatory effect of EGF on IL-1beta-induced IL-8 production was completely abolished by the broad range tyrosine kinase inhibitor Herbimycin A, and considerably reduced by the receptor tyrosine kinase specific inhibitor PD 153035. herbimycin 136-148 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 16678783-6 2006 Herbimycin A abolished IL-8 production induced by IL-1beta, whereas PD 153035 had no effect on the cytokine-induced IL-8 production. herbimycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 16678783-7 2006 Furthermore, the p38 mitogen-activated protein (MAP) kinase inhibitor SB 203580 reduced IL-8 production induced by IL-1beta as well as by the combination of EGF and IL-1beta but had no effect on EGF-induced IL-8 production. SB 203580 70-79 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 16963169-11 2006 However, the silica-induced up-regulation of IL-8 release through the SFK-ERK1/2 pathway does not appear to be initiated through activation of the EGFR, although basal EGFR activity may affect the magnitude of the responses. Silicon Dioxide 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 16806458-3 2006 Results indicate that a number of the primary carbon/resin materials demonstrate efficient adsorption of the cytokines studied here (TNF, IL-6 and IL-8), comparable to other adsorbents under clinical investigation. Carbon 46-52 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 16953188-3 2006 p38 MAPK may regulate cytokine production, therefore, the effect of two p38 MAPK inhibitors, SB239063 and SD-282, on the release of TNF-alpha, GM-CSF and IL-8 from human macrophages was investigated. SB 239063 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 16953188-3 2006 p38 MAPK may regulate cytokine production, therefore, the effect of two p38 MAPK inhibitors, SB239063 and SD-282, on the release of TNF-alpha, GM-CSF and IL-8 from human macrophages was investigated. indole-5-carboxamide 106-112 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 17066155-9 2006 An increased level of IL-8 during the third, fifth and seventh days of the investigation was seen in SABP patients. sabp 101-105 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 16837501-8 2006 In conclusion, thalidomide has the potential to improve the therapeutic regimens for sarcoidosis, hypersensitivity pneumonitis and idiopathic pulmonary fibrosis by reducing tumour necrosis factor-alpha, interleukin-12p40, interleukin-18 and interleukin-8 production. Thalidomide 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 241-254 17161617-0 2006 Salbutamol inhibits trypsin-mediated production of CXCL8 by keratinocytes. Albuterol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 51-56 17161617-2 2006 Production of CXCL8 was exquisitely sensitive to inhibition by co-treatment with the beta(2) agonist sabutamol (IC(50)=1.1 nM). sabutamol 101-110 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 17161617-4 2006 Salbutamol also elevated intracellular levels of cAMP (EC(50)=82 nM) but the relationship to the inhibition of CXCL8 secretion was not clear-cut since much higher concentrations of salbutamol were required to elevate total cellular cAMP than inhibit CXCL8 production. Albuterol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 250-255 17161617-6 2006 Potentiation of cAMP production by co-treatment with the phosphodiesterase type 4 inhibitor rolipram only marginally enhanced the inhibitory effect of salbutamol on CXCL8 production. Rolipram 92-100 C-X-C motif chemokine ligand 8 Homo sapiens 165-170 17161617-6 2006 Potentiation of cAMP production by co-treatment with the phosphodiesterase type 4 inhibitor rolipram only marginally enhanced the inhibitory effect of salbutamol on CXCL8 production. Albuterol 151-161 C-X-C motif chemokine ligand 8 Homo sapiens 165-170 17161617-7 2006 Taken together, these data suggest that elevation of cAMP production is required for the inhibitory effect of salbutamol on CXCL8 production by keratinocytes and that low threshold levels of cAMP are sufficient to mediate this effect. Cyclic AMP 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 124-129 17161617-7 2006 Taken together, these data suggest that elevation of cAMP production is required for the inhibitory effect of salbutamol on CXCL8 production by keratinocytes and that low threshold levels of cAMP are sufficient to mediate this effect. Albuterol 110-120 C-X-C motif chemokine ligand 8 Homo sapiens 124-129 17166736-5 2006 In PMA/ionomycin stimulated cells, pre-incubated with increasing concentrations of NIV, transcription was induced in the range 0.06-2 microM; higher concentrations of NIV were found non-stimulating (4 microM) or inhibitory (8 microM) for IFNgamma and IL-2 whereas IL-8 was still induced. Ionomycin 7-16 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 17166736-6 2006 DON administration elicited a similar profile for IL-8 and IFNgamma, whilst IL-2 mRNA was induced in a broader range of concentrations. deoxynivalenol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 17003352-7 2006 These findings implicate several factors in the insulin signaling pathway, which may be further dysregulated in HIV+IGT, and support the notion that insulin signaling pathways for glucose and leucine metabolism may be disrupted by increased proinflammatory adipocytokines (IL-8) and increased lipid oxidation. Glucose 180-187 C-X-C motif chemokine ligand 8 Homo sapiens 273-277 16837501-0 2006 Thalidomide reduces IL-18, IL-8 and TNF-alpha release from alveolar macrophages in interstitial lung disease. Thalidomide 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 16837501-6 2006 At the highest thalidomide concentration (0.1 mM), LPS-stimulated IL-8 production was also suppressed. Thalidomide 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 16837501-7 2006 In IPF patients, although spontaneous production of TNF-alpha, IL-12p40, IL-18 and IL-8 was lower than in sarcoidosis and HP patients, with LPS stimulation the cytokines were significantly elevated and also partially inhibited by thalidomide. Thalidomide 230-241 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 16715183-3 2006 In this study, we investigated the ability of homocysteine (Hcy) and homocysteine thiolactone (HcyT) to induce cell death and IL-8 secretion in primary human umbilical vein endothelial cells (HUVEC). Homocysteine 46-58 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16715183-3 2006 In this study, we investigated the ability of homocysteine (Hcy) and homocysteine thiolactone (HcyT) to induce cell death and IL-8 secretion in primary human umbilical vein endothelial cells (HUVEC). Homocysteine 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16715183-3 2006 In this study, we investigated the ability of homocysteine (Hcy) and homocysteine thiolactone (HcyT) to induce cell death and IL-8 secretion in primary human umbilical vein endothelial cells (HUVEC). homocysteine thiolactone 69-93 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16715183-3 2006 In this study, we investigated the ability of homocysteine (Hcy) and homocysteine thiolactone (HcyT) to induce cell death and IL-8 secretion in primary human umbilical vein endothelial cells (HUVEC). homocysteine thiolactone 95-99 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16545538-10 2006 The increased gene and protein expression of the pro-inflammatory cytokine IL-8, produced by endothelial cells, is likely in response to the manifestation of oxidative stress and GSH depletion; further amplifying the oxidative stress response induced by the fatty acid oxidation inhibitors and triggering an inflammatory response. Glutathione 179-182 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 17091205-10 2006 For interleukin-8, this decrease in concentration was smaller after the dust exposures spiked with glucan and aldehydes (-2.9 and -25.8 pg/ml, respectively) than after office dust or clean air (-65.9 and -74.1 pg/ml, respectively) (P=0.042). Glucans 99-105 C-X-C motif chemokine ligand 8 Homo sapiens 4-17 17091205-10 2006 For interleukin-8, this decrease in concentration was smaller after the dust exposures spiked with glucan and aldehydes (-2.9 and -25.8 pg/ml, respectively) than after office dust or clean air (-65.9 and -74.1 pg/ml, respectively) (P=0.042). Aldehydes 110-119 C-X-C motif chemokine ligand 8 Homo sapiens 4-17 16545538-10 2006 The increased gene and protein expression of the pro-inflammatory cytokine IL-8, produced by endothelial cells, is likely in response to the manifestation of oxidative stress and GSH depletion; further amplifying the oxidative stress response induced by the fatty acid oxidation inhibitors and triggering an inflammatory response. Fatty Acids 258-268 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 16581224-5 2006 Sodium nitrite at a low concentration (6.25 mM) increased IL-8 release, whereas IL-1 beta, IL-6, and TNF-alpha release increased only after exposure to high sodium nitrite concentration (25 mM). Sodium Nitrite 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 17096697-1 2006 In the present study, we examined whether the performance of hemoperfusion with an immobilized polymyxin B fiber column (DHP-PMX) reduces circulating interleukin-8 concentration in patients with sepsis. dhp-pmx 121-128 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 16984135-10 2006 When HUVEC were treated with TNF to induce inflammatory events, pretreatment with RGDPEG-SB-HSA partially inhibited proinflammatory gene expression (IL-8, E-selectin; 30% inhibition) and secretion of cytokines (IL-8, 34% inhibition). rgdpeg-sb-hsa 82-95 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 17096697-6 2006 Circulating interleukin-8 concentration was 55 +/- 15.7 pg/mL before DHP-PMX, while it was 101 +/- 58.8 pg/mL immediately after the first session of treatment. dhp-pmx 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 17096697-10 2006 The present findings indicate that DHP-PMX indirectly reduces circulating interleukin-8 concentration and improves SOFA score. dhp-pmx 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 16996012-0 2006 Effect of dexamethasone on the release of transforming growth factor-beta1, interleukin-8, interleukin-10 and RANTES release by sputum cells in severe asthma. Dexamethasone 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 16857333-7 2006 The inhibition of GHB production was apparent during storage in NaF treated frozen blood samples. 4-hydroxybutyric acid 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 16632517-3 2006 Blocking of gene transcription with actinomycin D suggested that NE stimulated IL-8 synthesis via increased mRNA expression, which was verified by real-time RT-PCR. Dactinomycin 36-49 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 16632517-5 2006 The results from the use of chemical inhibitors and mutant gene constructs against various signal transduction components seem to suggest the linear signaling pathway involving the activation of PKC-delta --> dual oxidase 1 --> reactive oxygen species --> TNF-alpha-converting enzyme --> EGF receptor --> p38 --> NF-kappaB for NE-activated IL-8 gene expression. Reactive Oxygen Species 234-257 C-X-C motif chemokine ligand 8 Homo sapiens 358-362 16842752-7 2006 Moreover, we found that SM-7409 strongly inhibits the LPS-induced other pro-inflammatory cytokines, such as interleukin (IL)-1beta and IL-8 in PBMCs. SM 7409 24-31 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 17000667-0 2006 Curcumin inhibits neurotensin-mediated interleukin-8 production and migration of HCT116 human colon cancer cells. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 17000667-10 2006 Moreover, curcumin blocked neurotensin-stimulated IL-8 gene induction and protein secretion and, at a low concentration (i.e., 10 micromol/L), blocked neurotensin-stimulated colon cancer cell migration. Curcumin 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 16870149-4 2006 Treatment of HeLa cells with apicidin leads to an increase in transcriptional activity of NF-kappaB and the expression of its target genes, IL-8 and TNF-alpha. apicidin 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 16581825-0 2006 Differential regulation of hyaluronan-induced IL-8 and IP-10 in airway epithelial cells. Hyaluronic Acid 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 16581825-5 2006 Furthermore, hyaluronan fragments use two distinct molecular pathways to induce IL-8 and IFN-gamma-inducible protein 10 (IP-10) chemokine expression in airway epithelial cells. Hyaluronic Acid 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 16581825-6 2006 Hyaluronan-induced IL-8 requires the MAP kinase pathway, whereas hyaluronan-induced IP-10 utilizes the NF-kappaB pathway. Hyaluronic Acid 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 16581825-9 2006 Furthermore, hyaluronan, by inducing IL-8 and IP-10 by distinct pathways, provides a unique target for differential regulation of key inflammatory chemokines. Hyaluronic Acid 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 16741151-0 2006 Azithromycin reduces airway neutrophilia and interleukin-8 in patients with bronchiolitis obliterans syndrome. Azithromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 16741151-4 2006 HYPOTHESES: (1) Azithromycin reduces airway neutrophilia and interleukin (IL)-8 and (2) airway neutrophilia predicts the improvement in FEV(1). Azithromycin 16-28 C-X-C motif chemokine ligand 8 Homo sapiens 61-79 16741151-11 2006 CONCLUSION: Azithromycin significantly reduces airway neutrophilia and IL-8 mRNA in patients with BOS. Azithromycin 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 16741151-11 2006 CONCLUSION: Azithromycin significantly reduces airway neutrophilia and IL-8 mRNA in patients with BOS. N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 16984135-10 2006 When HUVEC were treated with TNF to induce inflammatory events, pretreatment with RGDPEG-SB-HSA partially inhibited proinflammatory gene expression (IL-8, E-selectin; 30% inhibition) and secretion of cytokines (IL-8, 34% inhibition). rgdpeg-sb-hsa 82-95 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 16936090-6 2006 Triptolide and dexamethasone each inhibited in a concentration-dependent manner the LPS-induced release of IL-6, G-CSF, MCP-1, and IL-8 by corneal fibroblasts. Dexamethasone 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 16951177-8 2006 In addition, Src inhibition alone and in combination with docetaxel significantly down-regulated tumoral production of vascular endothelial growth factor and interleukin 8, whereas combination therapy decreased the microvessel density (P = 0.02) and significantly affected vascular permeability (P < 0.05). Docetaxel 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 17699316-9 2006 Serum IL-8 and TNF-alpha concentrations were significantly reduced by aspirin treatment at 4 mo (P = 0.04 and P = 0.007, respectively). Aspirin 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 16534530-13 2006 DISCUSSION: Our data demonstrated that the circulating levels of MCP-1 and IL-8 are related to obesity-related parameters such as BMI, waist circumference, CRP, IL-6, HOMA and HDL-cholesterol. Cholesterol 180-191 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 16936090-6 2006 Triptolide and dexamethasone each inhibited in a concentration-dependent manner the LPS-induced release of IL-6, G-CSF, MCP-1, and IL-8 by corneal fibroblasts. triptolide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 16624828-0 2006 1alpha, 25-dihydroxyvitamin D3 suppresses interleukin-8-mediated prostate cancer cell angiogenesis. Calcitriol 0-30 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 16807115-6 2006 IL-8 production from LPMC was significantly reduced by GC addition in responsive cases but not in refractory cases. lpmc 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16807115-8 2006 In addition, p38-MAPK antagonist SB230580 also ameliorated GC-resistant IL-8 production. sb230580 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16936090-10 2006 CONCLUSIONS: Triptolide inhibits the LPS-induced expression of IL-6, chemokines (G-CSF, MCP-1, IL-8), and ICAM-1 in cultured human corneal fibroblasts. triptolide 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 16775254-8 2006 We also show that cell-permeant C6 ceramide, like OxPAPC, causes the inhibition of LPS-induced IL-8 synthesis and alters caveolin distribution similar to OxPAPC. Ceramides 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 16920938-6 2006 In addition, As2O3 reduced expression of various macrophagic surface markers, enhanced that of the monocytic marker CD14, and altered both endocytosis and phagocytosis; unexpectedly, exposure of macrophages to the metalloid also strongly potentiated expression of TNFalpha and IL-8 induced by LPS. Arsenic Trioxide 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 277-281 17111070-10 2006 In an assay for inhibition of the H(2)O(2)-activated release of PGE2, IL-6, and IL-8 in normal human fibroblast cell lines, Ulmus davidiana root extract showed an inhibitory activity of PGE2 release in a dose-dependent manner (up to 85.9% at a concentration of 0.1%). Hydrogen Peroxide 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 17111070-10 2006 In an assay for inhibition of the H(2)O(2)-activated release of PGE2, IL-6, and IL-8 in normal human fibroblast cell lines, Ulmus davidiana root extract showed an inhibitory activity of PGE2 release in a dose-dependent manner (up to 85.9% at a concentration of 0.1%). Dinoprostone 186-190 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 16775254-1 2006 Previous studies from our laboratory and others presented evidence that oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylcholine (OxPAPC) and oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylethanolamine can inhibit lipopolysaccharide (LPS)-mediated induction of interleukin-8 (IL-8) in endothelial cells. 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylcholine 81-139 C-X-C motif chemokine ligand 8 Homo sapiens 285-298 16775254-1 2006 Previous studies from our laboratory and others presented evidence that oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylcholine (OxPAPC) and oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylethanolamine can inhibit lipopolysaccharide (LPS)-mediated induction of interleukin-8 (IL-8) in endothelial cells. 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylcholine 81-139 C-X-C motif chemokine ligand 8 Homo sapiens 300-304 16984733-7 2006 Following indomethacin treatment in breast cancer cells, several candidate genes, such as interleukin 8, NGFB, CSF2, RHOB, EDN1, and JUNB, were differentially expressed, which may have contributed to changes in choline metabolism through secondary effects or signaling cascades leading to changes in enzyme activity. Indomethacin 10-22 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 16775254-1 2006 Previous studies from our laboratory and others presented evidence that oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylcholine (OxPAPC) and oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylethanolamine can inhibit lipopolysaccharide (LPS)-mediated induction of interleukin-8 (IL-8) in endothelial cells. oxpapc 141-147 C-X-C motif chemokine ligand 8 Homo sapiens 285-298 16775254-1 2006 Previous studies from our laboratory and others presented evidence that oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylcholine (OxPAPC) and oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylethanolamine can inhibit lipopolysaccharide (LPS)-mediated induction of interleukin-8 (IL-8) in endothelial cells. oxpapc 141-147 C-X-C motif chemokine ligand 8 Homo sapiens 300-304 16775254-1 2006 Previous studies from our laboratory and others presented evidence that oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylcholine (OxPAPC) and oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylethanolamine can inhibit lipopolysaccharide (LPS)-mediated induction of interleukin-8 (IL-8) in endothelial cells. 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylethanolamine 162-225 C-X-C motif chemokine ligand 8 Homo sapiens 285-298 16775254-1 2006 Previous studies from our laboratory and others presented evidence that oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylcholine (OxPAPC) and oxidized 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylethanolamine can inhibit lipopolysaccharide (LPS)-mediated induction of interleukin-8 (IL-8) in endothelial cells. 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphatidylethanolamine 162-225 C-X-C motif chemokine ligand 8 Homo sapiens 300-304 17072061-4 2006 In this study we evaluated the influence of N-acetylcysteine (NAC) (0.01 mM-30 mM) on the cytokine-induced (TNF-alpha/IL-1 beta) expression of the ICAM-1 adhesion molecule and on IL-8 release in endothelial (ECV-304) and bronchial epithelial (H292) cell lines. Acetylcysteine 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 17072061-6 2006 NAC inhibited the TNF-alpha/IL-1 beta-stimulated ICAM-1 expression and IL-8 release from both cell lines in a concentration dependent manner. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 17072061-8 2006 We conclude that NAC is an effective inhibitor of TNF-alpha/IL-1 beta- stimulated ICAM-1 and IL-8 release in endothelial and epithelial cells. Acetylcysteine 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 16984733-7 2006 Following indomethacin treatment in breast cancer cells, several candidate genes, such as interleukin 8, NGFB, CSF2, RHOB, EDN1, and JUNB, were differentially expressed, which may have contributed to changes in choline metabolism through secondary effects or signaling cascades leading to changes in enzyme activity. Choline 211-218 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 16621025-0 2006 Induction of interleukin-8 expression in porcine peripheral blood mononuclear cells by trans10-cis12 conjugated linoleic acid. Linoleic Acid 112-125 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 16448811-0 2006 Inhibition of pyocyanin-potentiated IL-8 release by steroids in bronchial epithelial cells. Pyocyanine 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 16448811-0 2006 Inhibition of pyocyanin-potentiated IL-8 release by steroids in bronchial epithelial cells. Steroids 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 16448811-2 2006 Pyocyanin-induced synergism with interleukin (IL)-1 or tumour necrosis factor (TNF) in triggering IL-8 release has been documented previously. Pyocyanine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 16448811-3 2006 In this study, IL-8 mRNA and protein expression were examined in cultured human bronchial epithelial cells (BEAS-2B) stimulated with pyocyanin alone, and in combination with IL-1beta or phorbol 12,13-dibutyrate (PDBu) in the absence and presence of a group of glucocorticoids. Pyocyanine 133-142 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 16448811-6 2006 However, pyocyanin upregulated the stimulatory effect of IL-1beta or PDBu on the release of IL-8 in a dose-dependent manner. Pyocyanine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 16448811-7 2006 The stimulatory effect of pyocyanin on the IL-1beta- or PDBu-stimulated IL-8 release was reduced in the presence of dexamethasone, budesonide, and fluticasone. Pyocyanine 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16448811-7 2006 The stimulatory effect of pyocyanin on the IL-1beta- or PDBu-stimulated IL-8 release was reduced in the presence of dexamethasone, budesonide, and fluticasone. Dexamethasone 116-129 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16448811-7 2006 The stimulatory effect of pyocyanin on the IL-1beta- or PDBu-stimulated IL-8 release was reduced in the presence of dexamethasone, budesonide, and fluticasone. Budesonide 131-141 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16448811-7 2006 The stimulatory effect of pyocyanin on the IL-1beta- or PDBu-stimulated IL-8 release was reduced in the presence of dexamethasone, budesonide, and fluticasone. Fluticasone 147-158 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16448811-9 2006 The protein kinase C (PKC) inhibitor, Go6976, also significantly reduced the stimulatory effect of pyocyanin on IL-1beta, and PDBu increased IL-8 release. Go 6976 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 16448811-10 2006 In conclusion, this study shows that PKC signal pathway seems to be involved in the pyocyanin-mediated upregulation of the IL-1beta and PDBu-induced IL-8 release in BEAS-2B cells. Pyocyanine 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 16469490-9 2006 Blocking rho kinase using Y-27632 inhibited the effect of stretch on IL-8 release by the BEAS 2B cells. Y 27632 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 16937534-2 2006 METHODS: IL-8 -251 A/T polymorphism was genotyped by oligonucleotide allele specific PCR (ASO-PCR) in a sample of 233 patients with H pylori infection undergoing upper gastrointestinal endoscopy. Oligonucleotides 53-68 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 16912112-1 2006 Oxidized phospholipids are thought to promote atherogenesis by stimulating endothelial cells (ECs) to produce inflammatory cytokines, such as IL-8. Phospholipids 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 16937467-10 2006 Although all three MAP kinase family members were phosphorylated in response to TNF-alpha, a selective inhibitor of p38 kinase SB203580 only could inhibit both NF-kappaB-dependent transcriptional activity and IL-8 and CCL20 production, suggesting a potential link between p38 kinase and NF-kappaB-dependent pathways in AGS cells. SB 203580 127-135 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 17075545-2 2006 In vitro studies have demonstrated the anti-inflammatory effects of macrolides: decreased productions of IL-6, IL-8, TNF alpha, chemotactism of polymorphonuclear neutrophils. Macrolides 68-78 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 16948846-5 2006 Two of these four compounds, alpha-mangostin and 18-beta-glycyrrhetinic acid, activated NFkappaB and induced IL-8 secretion. mangostin 29-44 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 16948846-5 2006 Two of these four compounds, alpha-mangostin and 18-beta-glycyrrhetinic acid, activated NFkappaB and induced IL-8 secretion. 18alpha-glycyrrhetinic acid 49-76 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 16621025-6 2006 This study strongly suggests that the immunoenhancing effect of CLA on the chemotactic response of porcine PMN is mediated through IL-8 produced by CLA treated PBMC. Linoleic Acids, Conjugated 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 16239062-2 2006 RA also reduced intracellular reactive oxygen species (ROS) level, H2O2-dependent VEGF expression and IL-8 release of endothelial cells. rosmarinic acid 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 16239062-3 2006 These findings suggested that the anti-angiogenic potential of RA might be related to its anti-oxidative activity, which further resulted in the inhibition of ROS-associated VEGF expression and IL-8 release. rosmarinic acid 63-65 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 16621025-6 2006 This study strongly suggests that the immunoenhancing effect of CLA on the chemotactic response of porcine PMN is mediated through IL-8 produced by CLA treated PBMC. Linoleic Acids, Conjugated 148-151 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 16697193-1 2006 A novel series of 3,4-diaminocyclobut-3-ene-1,2-diones was prepared and found to show potent inhibitory activity of CXCR2 binding and IL-8-mediated chemotaxis of a CXCR2-expressing cell line. 3,4-diaminocyclobut-3-ene-1,2-dione 18-54 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 16485121-5 2006 The lowest HEK mortality (7%) and the highest IL-8 production were induced with mixtures including high cytotoxic and weak IL-8 inductive ARO hydrocarbons. Hydrocarbons, Aromatic 138-154 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 16485121-5 2006 The lowest HEK mortality (7%) and the highest IL-8 production were induced with mixtures including high cytotoxic and weak IL-8 inductive ARO hydrocarbons. Hydrocarbons, Aromatic 138-154 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 16485121-7 2006 Single addition of benzene, toluene, xylene or ethylbenzene for up to tenfold in JP-8 did not increase HEK mortality while single addition of ALI hydrocarbons exhibited dose-related differential response in IL-8. ali hydrocarbons 142-158 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 16485121-8 2006 In an all ALI environment, no single hydrocarbon is the dominating factor in the determination of HEK cytotoxicity while deletion of hexadecane resulted in a 2.5-fold increase in IL-8 production. n-hexadecane 133-143 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 16861626-5 2006 Eight months following treatment with a single dose of ivermectin-albendazole, some of these defects were reversed, with monocyte production of IL-8, IL-1alpha, MIP-1alpha, and IL-10 being comparable to that seen in the uninfected controls. ivermectin-albendazole 55-77 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 16798838-4 2006 The tyrosine kinase inhibitor Tyrphostin A9, phosphatidylinositol-3 kinase (PI3K) inhibitor LY294002 as well as proteasome inhibitors significantly blocked the CXCL8-induced chemotaxis of L1.2 cells and human neutrophils. tyrphostin A9 30-43 C-X-C motif chemokine ligand 8 Homo sapiens 160-165 16798838-4 2006 The tyrosine kinase inhibitor Tyrphostin A9, phosphatidylinositol-3 kinase (PI3K) inhibitor LY294002 as well as proteasome inhibitors significantly blocked the CXCL8-induced chemotaxis of L1.2 cells and human neutrophils. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 92-100 C-X-C motif chemokine ligand 8 Homo sapiens 160-165 16798838-9 2006 The CXCL8-induced phosphorylation of Cbl was also reduced when cells were pre-treated with the PI3K inhibitor LY294002. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 110-118 C-X-C motif chemokine ligand 8 Homo sapiens 4-9 16798838-10 2006 Lastly, we have shown that pre-treatment of L1.2 cells with the proteasome inhibitor Lactacystin blocks CXCL8-induced internalization of the CXCR1 and CXCR2 receptors. lactacystin 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 104-109 16911361-7 2006 RESULTS: Real-time PCR revealed that poly I : C significantly increased the expression of mRNAs for chemokines IP-10, RANTES, LARC, MIP-1alpha, IL-8, GRO-alpha and ENA-78 and cytokines IL-1beta, GM-CSF, IL-6 and the cell adhesion molecule ICAM-1 in both cell types. Poly I 37-43 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 16907497-1 2006 We report the first observation of anti-Stokes laser-induced cooling in the Er3+:KPb2Cl5 crystal and in the Er3+:CNBZn (CdF2-CdCl2-NaF-BaF2-BaCl2-ZnF2) glass. cnbzn 113-118 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 16491109-8 2006 RESULTS: Subjects receiving folic acid supplementation showed a decrement of homocysteine and an amelioration of insulin sensitivity; this treatment was also associated with a significant drop in the circulating concentration of monocyte chemoattractant protein-1, interleukin-8 and C-reactive protein, in the absence of any significant variation of BMI or fat mass. Folic Acid 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 265-278 16884979-14 2006 CONCLUSION: Sevoflurane suppressed the production of IL-6 and IL-8, but not IL-10 and IL-1ra. Sevoflurane 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 16769764-0 2006 IL-6 and IL-8 release is mediated via multiple signaling pathways after stimulating dendritic cells with lysophospholipids. Lysophospholipids 105-122 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 16797033-0 2006 Effect of berberrubine on interleukin-8 and monocyte chemotactic protein-1 expression in human retinal pigment epithelial cell line. berberrubine 10-22 C-X-C motif chemokine ligand 8 Homo sapiens 26-39 16797033-1 2006 We examined the effects of berberrubine, a protoberberine alkaloid, on interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) expression in a human retinal pigment epithelial cell line (ARPE-19) stimulated with interleukin-1beta (IL-1beta) or tumor necrosis factor alpha (TNF-alpha). berberrubine 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 16797033-7 2006 Berberrubine dose-dependently inhibited IL-8 and MCP-1 protein levels in the media and mRNA expression of the cells stimulated with IL-1beta or TNF-alpha. berberrubine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 16797033-10 2006 Berberrubine dose-dependently inhibited IL-8 and MCP-1 expression and protein secretion induced by IL-1beta or TNF-alpha. berberrubine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 16842506-8 2006 In addition, IL-8 (or an analogue) was found in the candidal mother cell in chronic hyperplastic candidosis and in agar, whereas the tips of the hyphae expressed IL-8 receptor A (or an analogue). Agar 115-119 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 16687414-0 2006 Regulation of lysophosphatidic acid-induced epidermal growth factor receptor transactivation and interleukin-8 secretion in human bronchial epithelial cells by protein kinase Cdelta, Lyn kinase, and matrix metalloproteinases. lysophosphatidic acid 14-35 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 16614347-6 2006 LPS-induced release of 10 cytokines was less suppressed by dexamethasone (10(-6) M) in patients with severe asthma compared with patients with nonsevere asthma, with statistical significance achieved for IL-1beta (p < 0.03), IL-8 (p < 0.03), and MIP-1alpha (p < 0.003), and borderline significance for IL-6 (p = 0.054). Dexamethasone 59-72 C-X-C motif chemokine ligand 8 Homo sapiens 228-232 16834783-14 2006 Like dexamethasone and mometasone, RU24858 did suppress IL-8 and MCP-1 production in eosinophils. RU24858 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 16834785-7 2006 Inhibition of JNK by small molecule inhibitor SP600125 reduced pneumococci-induced IL-8 mRNA expression and release of IL-8 and IL-6. pyrazolanthrone 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 16834785-7 2006 Inhibition of JNK by small molecule inhibitor SP600125 reduced pneumococci-induced IL-8 mRNA expression and release of IL-8 and IL-6. pyrazolanthrone 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 16801185-12 2006 Serum interleukin -8 may be useful in assessing the therapeutic effects of cyclosporine A in hyperzincaemia and hypercalprotectinaemia. Cyclosporine 75-89 C-X-C motif chemokine ligand 8 Homo sapiens 6-20 16687414-7 2006 Furthermore, down-regulation of EGFR by EGFR small interfering RNA or pretreatment of cells with EGFR inhibitors AG1478 and PD158780 almost completely blocked LPA-dependent EGFR phosphorylation and partially attenuated IL-8 secretion, respectively. RTKI cpd 113-119 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 16687414-7 2006 Furthermore, down-regulation of EGFR by EGFR small interfering RNA or pretreatment of cells with EGFR inhibitors AG1478 and PD158780 almost completely blocked LPA-dependent EGFR phosphorylation and partially attenuated IL-8 secretion, respectively. 6-(methylamino)pyrido(3,4-d)pyrimidine 124-132 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 16687414-8 2006 These results demonstrate that LPA-induced IL-8 secretion is partly dependent on EGFR transactivation regulated by PKCdelta-dependent activation of Lyn kinase and MMPs and proHB-EGF shedding, suggesting a novel mechanism of cross-talk and interaction between G-protein-coupled receptors and receptor-tyrosine kinases in HBEpCs. lysophosphatidic acid 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 16687414-1 2006 We have demonstrated earlier that lysophosphatidic acid (LPA)-induced interleukin-8 (IL-8) secretion is regulated by protein kinase Cdelta (PKCdelta)-dependent NF-kappaB activation in human bronchial epithelial cells (HBEpCs). lysophosphatidic acid 34-55 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 16687414-1 2006 We have demonstrated earlier that lysophosphatidic acid (LPA)-induced interleukin-8 (IL-8) secretion is regulated by protein kinase Cdelta (PKCdelta)-dependent NF-kappaB activation in human bronchial epithelial cells (HBEpCs). lysophosphatidic acid 34-55 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 16687414-1 2006 We have demonstrated earlier that lysophosphatidic acid (LPA)-induced interleukin-8 (IL-8) secretion is regulated by protein kinase Cdelta (PKCdelta)-dependent NF-kappaB activation in human bronchial epithelial cells (HBEpCs). lysophosphatidic acid 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 16687414-1 2006 We have demonstrated earlier that lysophosphatidic acid (LPA)-induced interleukin-8 (IL-8) secretion is regulated by protein kinase Cdelta (PKCdelta)-dependent NF-kappaB activation in human bronchial epithelial cells (HBEpCs). lysophosphatidic acid 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 16473865-3 2006 The aim of this study was to investigate the molecular mechanism(s) of inflammatory responses caused by cigarette smoke extract (CSE) in the human macrophage-like cell line MonoMac6 and whether the treatment of these cells with the antioxidant glutathione (GSH) monoethyl ester, or modulation of the thioredoxin redox system, can attenuate cigarette smoke-mediated IL-8 release. Glutathione 244-255 C-X-C motif chemokine ligand 8 Homo sapiens 365-369 16473865-8 2006 Pretreatment of cells with GSH monoethyl ester, but not thioredoxin/thioredoxin reductase, reversed cigarette smoke-induced reduction in HDAC levels and significantly inhibited IL-8 release. gsh monoethyl ester 27-46 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 16687414-2 2006 Here we provide evidence for signaling pathways that regulate LPA-mediated transactivation of epidermal growth factor receptor (EGFR) and the role of cross-talk between G-protein-coupled receptors and receptor-tyrosine kinases in IL-8 secretion in HBEpCs. lysophosphatidic acid 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 16522819-4 2006 Adenosine compounds also desensitized IL-8- and MCP-1-induced chemotaxis, but not that induced by fMLP. Adenosine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 38-43 16945263-6 2006 IL-8, leukotriene B4, and 8-isoprostano in EBC correlated significantly with DLCO/VA (% of predicted) (r = 0.30, P < .05; r = 0.29, P < or = .05; and r = 0.46, P < .01, respectively) but not with forced expiratory volume in 1 second. NSC638702 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16945263-7 2006 There was a negative correlation between EBC and serum levels of both IL-8 (r = -0.31; P < .05) and 8-isoprostane (r = -0.51; P < .001). NSC638702 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 16819191-7 2006 Furthermore, curcumin significantly attenuated Stx-1 induced cell death and IL-8 expression. Curcumin 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 16956428-7 2006 Hcy enhanced IL-6 and IL-8 production in RA synoviocytes only (up to 35%). Homocysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 16283305-4 2006 TMV also carried mRNA for growth factors: vascular endothelial growth factor (VEGF), hepatocyte growth factor (HGF), interleukin-8 (IL-8) and surface determinants (CD44H). tmv 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 16283305-4 2006 TMV also carried mRNA for growth factors: vascular endothelial growth factor (VEGF), hepatocyte growth factor (HGF), interleukin-8 (IL-8) and surface determinants (CD44H). tmv 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 16723241-1 2006 OBJECTIVE: Lactate levels after cardiac surgery are influenced by different proinflammatory (TNF, IL-6, IL-8) and anti-inflammatory (IL-10) cytokines. Lactic Acid 11-18 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 17077666-7 2006 In contrast, Dex treatment inhibited the IL-1beta-induced production of GM-CSF, IL-6, IL-8, MCP-3, and RANTES, but not MCP-1. Dexamethasone 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 16949835-0 2006 Roles of p38 and ERK MAP kinases in IL-8 expression in TNF-alpha- and dexamethasone-stimulated human periodontal ligament cells. Dexamethasone 70-83 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 16949835-3 2006 In this study, we investigated the role of mitogen-activated protein (MAP) kinases in dexamethasone- and TNF-alpha-induced IL-8 and ICAM-1 expression in hPDL cells. Dexamethasone 86-99 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 16949835-7 2006 Dexamethasone suppressed TNF-alpha-induced IL-8 production in a dose-dependent manner. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 16949835-10 2006 Furthermore, these results suggest that inflammatory cytokine- and dexamethasone-induced IL-8 and ICAM-1, produced via a MAP kinase pathway, may serve as an important mediator of PDL immunoregulation involved in bone remodeling during orthodontic tooth movement. Dexamethasone 67-80 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 16761312-5 2006 sPLA(2) induced the phosphorylation of the MAPK p38 and ERK1/2, and inhibition of these kinases by SB203580 and PD98059, respectively, reduced TNF-alpha and CXCL8 release. SB 203580 99-107 C-X-C motif chemokine ligand 8 Homo sapiens 157-162 16714014-0 2006 Cannabinoid signalling in TNF-alpha induced IL-8 release. Cannabinoids 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 16723156-0 2006 High dose of intravenously given glucocorticosteroids decrease IL-8 production by monocytes in multiple sclerosis patients treated during relapse. glucocorticosteroids 33-53 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 16761312-5 2006 sPLA(2) induced the phosphorylation of the MAPK p38 and ERK1/2, and inhibition of these kinases by SB203580 and PD98059, respectively, reduced TNF-alpha and CXCL8 release. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 157-162 16761312-7 2006 GIA activated the phosphatidylinositol 3-kinase (PI3 K)/Akt system and a specific inhibitor of PI3 K (LY294002) reduced sPLA(2)-induced release of TNF-alpha and CXCL8. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 102-110 C-X-C motif chemokine ligand 8 Homo sapiens 161-166 16761312-8 2006 GIA promoted phosphorylation and degradation of IkappaB and inhibition of NF-kappaB by MG-132 and 6-amino-4-phenoxyphenylethylamino-quinazoline suppressed the production of TNF-alpha and CXCL8. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 87-93 C-X-C motif chemokine ligand 8 Homo sapiens 187-192 16761312-8 2006 GIA promoted phosphorylation and degradation of IkappaB and inhibition of NF-kappaB by MG-132 and 6-amino-4-phenoxyphenylethylamino-quinazoline suppressed the production of TNF-alpha and CXCL8. 6-amino-4-phenoxyphenylethylamino-quinazoline 98-143 C-X-C motif chemokine ligand 8 Homo sapiens 187-192 16804397-6 2006 Muramyl dipeptide-induced enhancement of interleukin (IL)-8 secretion and synergistic increase in lipopolysaccharide-induced IL-1beta secretion were studied. Acetylmuramyl-Alanyl-Isoglutamine 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 41-59 16804397-8 2006 RESULTS: The assay was highly sensitive and specific for detection of profound defects in muramyl dipeptide sensing caused by double NOD2 mutations (IL-8 P = 0.0002; IL-1beta P = 0.0002). Dipeptides 98-107 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 16804397-10 2006 Healthy NOD2 heterozygotes had modest impairment of muramyl dipeptide induced IL-8 secretion (P = 0.003). muramyl 52-59 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 16804397-10 2006 Healthy NOD2 heterozygotes had modest impairment of muramyl dipeptide induced IL-8 secretion (P = 0.003). Dipeptides 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 16804400-8 2006 Interestingly, gliotoxin induced HO-1 in HT-29 cells and, in turn, inhibition of HO-1 activity by a zinc protoporphyrin IX reversed the effects of gliotoxin in terms of I-kappaB degradation, intercellular adhesion molecule-1 expression, and IL-8 production. Gliotoxin 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 16804400-8 2006 Interestingly, gliotoxin induced HO-1 in HT-29 cells and, in turn, inhibition of HO-1 activity by a zinc protoporphyrin IX reversed the effects of gliotoxin in terms of I-kappaB degradation, intercellular adhesion molecule-1 expression, and IL-8 production. zinc protoporphyrin 100-122 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 16804400-8 2006 Interestingly, gliotoxin induced HO-1 in HT-29 cells and, in turn, inhibition of HO-1 activity by a zinc protoporphyrin IX reversed the effects of gliotoxin in terms of I-kappaB degradation, intercellular adhesion molecule-1 expression, and IL-8 production. Gliotoxin 147-156 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 16723156-4 2006 IL-8 is one of the cytokines responsible for blood-brain-barrier disruption and migration of immune cells to the central nervous system; in this aspect, explaining glucocorticosteroid effects during MS exacerbations. glucocorticosteroid 164-183 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16621797-7 2006 Inhibition of the proteasome with bortezomib (PS-341/Velcade) also rescued CFTR, but with less efficiency, and suppressed NFkappaB-mediated IL8 activation. Bortezomib 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 140-143 17013434-5 2006 It has been demonstrated that thalidomide inhibits TNFalpha, IL-5, IL-6, IL-8, IL-12 production and increases production of IL-2, IL-10 and INFgamma. Thalidomide 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 16611624-0 2006 c-Src is the primary signaling mediator of polychlorinated biphenyl-induced interleukin-8 expression in a human microvascular endothelial cell line. Polychlorinated Biphenyls 43-67 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 16611624-2 2006 Therefore, the present study focused on the regulatory mechanisms of IL-8 expression induced by environmental pollutants such as polychlorinated biphenyls (PCBs). Polychlorinated Biphenyls 129-154 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 16611624-2 2006 Therefore, the present study focused on the regulatory mechanisms of IL-8 expression induced by environmental pollutants such as polychlorinated biphenyls (PCBs). Polychlorinated Biphenyls 156-160 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 16611624-3 2006 Treatment of human microvascular endothelial cells (HMECs) with specific PCB congener, 2,2",4,6,6"-pentachlorobiphenyl (PCB 104), dose dependently increased levels of IL-8 mRNA and secreted protein. 2,2',4,6,6'-pentachlorobiphenyl 87-118 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 16678856-13 2006 Treatment with the COX-2 inhibitor NS-398 at a low 1-mu[scap]M dose reduced the production of IL-8 in COX-2-transfected MDA-231 cells by 30%, thus confirming the involvement of COX-2 in IL-8 induction. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 35-41 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16678856-13 2006 Treatment with the COX-2 inhibitor NS-398 at a low 1-mu[scap]M dose reduced the production of IL-8 in COX-2-transfected MDA-231 cells by 30%, thus confirming the involvement of COX-2 in IL-8 induction. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 35-41 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 16784240-0 2006 Probing receptor binding activity of interleukin-8 dimer using a disulfide trap. Disulfides 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 16621797-8 2006 The inhibition of the major stress-inducible transcription factor CHOP (CCAAT/enhancer-binding protein homologous protein)/GADD153 together with bortezomib was most effective in repressing NFkappaB-mediated IL8 activation compared with interference of VCP, MLN-273 (proteasome inhibitor), or 4-phenylbutyrate (histone deacetylase inhibitor). gadd153 123-130 C-X-C motif chemokine ligand 8 Homo sapiens 207-210 16800483-0 2006 Formation of porous carbon materials with in situ generated NaF nanotemplate. Carbon 20-26 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 16800483-1 2006 Porous carbon materials with pore sizes from 3 to 200 nm were synthesized by reacting hexafluorobenzene with Na liquid at 623 K. NaF crystals, a byproduct formed in the reaction, acted as nanotemplate to assist the pore formation. Carbon 7-13 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 16800483-1 2006 Porous carbon materials with pore sizes from 3 to 200 nm were synthesized by reacting hexafluorobenzene with Na liquid at 623 K. NaF crystals, a byproduct formed in the reaction, acted as nanotemplate to assist the pore formation. hexafluorobenzene 86-103 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 16621797-8 2006 The inhibition of the major stress-inducible transcription factor CHOP (CCAAT/enhancer-binding protein homologous protein)/GADD153 together with bortezomib was most effective in repressing NFkappaB-mediated IL8 activation compared with interference of VCP, MLN-273 (proteasome inhibitor), or 4-phenylbutyrate (histone deacetylase inhibitor). Bortezomib 145-155 C-X-C motif chemokine ligand 8 Homo sapiens 207-210 16621797-8 2006 The inhibition of the major stress-inducible transcription factor CHOP (CCAAT/enhancer-binding protein homologous protein)/GADD153 together with bortezomib was most effective in repressing NFkappaB-mediated IL8 activation compared with interference of VCP, MLN-273 (proteasome inhibitor), or 4-phenylbutyrate (histone deacetylase inhibitor). N-(4-morpholine)carbonyl-beta-(1-naphthyl)-alanyl-leucine boronic acid 257-264 C-X-C motif chemokine ligand 8 Homo sapiens 207-210 16621797-8 2006 The inhibition of the major stress-inducible transcription factor CHOP (CCAAT/enhancer-binding protein homologous protein)/GADD153 together with bortezomib was most effective in repressing NFkappaB-mediated IL8 activation compared with interference of VCP, MLN-273 (proteasome inhibitor), or 4-phenylbutyrate (histone deacetylase inhibitor). 4-phenylbutyric acid 292-308 C-X-C motif chemokine ligand 8 Homo sapiens 207-210 16650380-0 2006 Effect of herbal melanin on IL-8: a possible role of Toll-like receptor 4 (TLR4). Melanins 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 16650380-2 2006 In this study, we tested the effect of a herbal melanin (HM) extract, from black cumin seeds (Nigella sativa L.), on IL-8 production. Melanins 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 16650380-3 2006 We used HM and LPS in parallel to induce IL-8 production by THP-I, PBMCs, and TLR4-transfected HEK293 cells. His-Met 8-10 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 16650380-5 2006 On applying similar treatment to HEK293 cells that express TLR4, MD2, and CD14, both HM and LPS significantly induced IL-8 protein production. His-Met 85-87 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 16650380-6 2006 We have also demonstrated that HM and LPS had identical effects in terms of IL-8 stimulation by HEK293 transfected with either TLR4 or MD2-CD14. His-Met 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 16650380-7 2006 Melanin extracted from N. sativa L. mimics the action of LPS in the induction of IL-8 by PBMC and the other used cell lines. Melanins 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 16541418-8 2006 TGF-beta1 stimulated IL-8 expression in dose- and time-dependent manners, which was blocked by cycloheximide (CHX) and actinomycin D (ActD). Cycloheximide 95-108 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 16364386-10 2006 Taken together, these data suggest that (1) p38 activation was required for induction of IL-8 and proinflammatory gene expression in the monocyte and (2) DON induced p38 activation in human monocytes via the ribotoxic stress response. deoxynivalenol 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 16364386-0 2006 p38 Mitogen-activated protein kinase mediates IL-8 induction by the ribotoxin deoxynivalenol in human monocytes. ribotoxin 68-77 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 16364386-0 2006 p38 Mitogen-activated protein kinase mediates IL-8 induction by the ribotoxin deoxynivalenol in human monocytes. deoxynivalenol 78-92 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 16364386-1 2006 The effects of the ribotoxic trichothecene deoxynivalenol (DON) on mitogen-activated protein kinase (MAPK)-mediated IL-8 expression were investigated in cloned human monocytes and peripheral blood mononuclear cells (PBMC). deoxynivalenol 43-57 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 16541418-8 2006 TGF-beta1 stimulated IL-8 expression in dose- and time-dependent manners, which was blocked by cycloheximide (CHX) and actinomycin D (ActD). Cycloheximide 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 16364386-1 2006 The effects of the ribotoxic trichothecene deoxynivalenol (DON) on mitogen-activated protein kinase (MAPK)-mediated IL-8 expression were investigated in cloned human monocytes and peripheral blood mononuclear cells (PBMC). deoxynivalenol 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 16364386-2 2006 DON (250 to 1000 ng/ml) induced both IL-8 mRNA and IL-8 heteronuclear RNA (hnRNA), an indicator of IL-8 transcription, in the human U937 monocytic cell line in a concentration-dependent manner. deoxynivalenol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 16364386-2 2006 DON (250 to 1000 ng/ml) induced both IL-8 mRNA and IL-8 heteronuclear RNA (hnRNA), an indicator of IL-8 transcription, in the human U937 monocytic cell line in a concentration-dependent manner. deoxynivalenol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 16541418-8 2006 TGF-beta1 stimulated IL-8 expression in dose- and time-dependent manners, which was blocked by cycloheximide (CHX) and actinomycin D (ActD). Dactinomycin 119-132 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 16364386-2 2006 DON (250 to 1000 ng/ml) induced both IL-8 mRNA and IL-8 heteronuclear RNA (hnRNA), an indicator of IL-8 transcription, in the human U937 monocytic cell line in a concentration-dependent manner. deoxynivalenol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 16364386-3 2006 Expression of IL-8 hnRNA, mRNA and protein correlated with p38 phosphorylation and was completely abrogated by the p38 MAPK inhibitor SB203580. SB 203580 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16364386-4 2006 DON at 500 ng/ml similarly induced p38-dependent IL-8 protein and mRNA expression in PBMC cultures from healthy volunteers. deoxynivalenol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 16541418-8 2006 TGF-beta1 stimulated IL-8 expression in dose- and time-dependent manners, which was blocked by cycloheximide (CHX) and actinomycin D (ActD). Dactinomycin 134-138 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 16414982-2 2006 Inhibition of the Erk MAPK, MEK, by U0126 produces a marked decrease in NaF-induced caldesmon phosphorylation. U 0126 36-41 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 16620783-8 2006 IL-1beta-pretreated NT2-N induced the chemotaxis of PBMC, which was significantly reduced by anti-IL-8, but not by anti-MIP-1beta neutralizing antibody. nt2-n 20-25 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 16684953-9 2006 The decay of IL-8 mRNA transcripts proceeded at a significantly faster rate when cells were pretreated with the p38 MAPK inhibitor SB-203580 (-0.05763 +/- 0.01964, t(1/2) = 12.0 h), compared with vehicle (-0.01030 +/- 0.007963, t(1/2) = 67.3 h) [results are expressed as decay constant (means +/- SE) and half-life (t(1/2) in h): P < 0.05]. SB 203580 131-140 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 16414982-4 2006 Selective Raf-1 inhibitors (ZM-336372 and Raf-1 inhibitor 1) significantly attenuate NaF-induced Erk and caldesmon phosphorylation. N-(5-(3-dimethylaminobenzamido)-2-methylphenyl)-4-hydroxybenzamide 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 16414982-7 2006 Pretreatment with KN93, a specific CaMKII inhibitor, attenuates NaF-induced barrier dysfunction and Erk phosphorylation. KN 93 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 16734624-8 2006 IL-8, GRO-alpha and ENA-78 synthesis was suppressed almost completely by AEBSF and BAY 11-7085, whereas prednisolone reduced chemokine levels differentially dependent on the supernatant added. 4-(2-aminoethyl)benzenesulfonylfluoride 73-78 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16755003-0 2006 Inhibition of IL-8 production by green tea polyphenols in human nasal fibroblasts and A549 epithelial cells. Polyphenols 43-54 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16755003-8 2006 Tea polyphenols were very effective in the inhibition of IL-8 production. Polyphenols 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 16755003-11 2006 Production of IL-8 after stimulation by proinflammatory cytokines in both nasal fibroblasts and bronchial epithelial cells was significantly blocked by pretreatment with green tea polyphenols. Polyphenols 180-191 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16736518-6 2006 RESULTS: ICs containing anti-CII from arthritis patients induced the production of tumor necrosis factor alpha (TNFalpha), interleukin-1beta (IL-1beta), and IL-8. N-[(1S)-2-methyl-1-(pyridin-4-ylcarbamoyl)propyl]cyclohexanecarboxamide 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 16736518-9 2006 Anti-CII-containing IC-induced cytokine production was almost totally abolished (>99%) after monocyte depletion, and receptor blocking studies showed significant decreases in the production of TNFalpha, IL-1beta, and IL-8 after blocking Fc gammaRIIa, but not after blocking Fc gammaRIII. N-[(1S)-2-methyl-1-(pyridin-4-ylcarbamoyl)propyl]cyclohexanecarboxamide 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 220-224 16778290-9 2006 In support, native and polymeric AAT-M with low endotoxin contamination completely inhibited neutrophil IL-8 release triggered by the zymosan, while AATs with high endotoxin contamination strongly induced IL-8 release and did not inhibit zymosan-stimulated IL-8 release. Zymosan 134-141 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 16734624-8 2006 IL-8, GRO-alpha and ENA-78 synthesis was suppressed almost completely by AEBSF and BAY 11-7085, whereas prednisolone reduced chemokine levels differentially dependent on the supernatant added. BAY 11-7085 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16916238-2 2006 Acetic acid was added to a 0.1% NaF solution to make two solutions, one with pH 3.5 and the other with pH 6. Acetic Acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 16955241-1 2006 OBJECTIVE: To investigate whether FK506 (tacrolimus) can inhibit Fas- or A23187-induced interleukin (IL)-8 expression and cell death in A549 human alveolar epithelial cells, plus Fas-mediated acute lung injury in vivo. Tacrolimus 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 88-106 16637007-5 2006 M-TriDAP induced IL-8/TNF-alpha secretion, and enhancement of LPS IL-1beta responses was significantly reduced between NOD2 double mutation carriers versus healthy controls, whereas there was no difference with FK565 or TriDAP stimulation, or between 1007fs/1007fs cells and other genotypes. L-Ala-gamma-D-Glu-meso-diaminopimelic acid 2-8 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 16955241-1 2006 OBJECTIVE: To investigate whether FK506 (tacrolimus) can inhibit Fas- or A23187-induced interleukin (IL)-8 expression and cell death in A549 human alveolar epithelial cells, plus Fas-mediated acute lung injury in vivo. Tacrolimus 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 88-106 16955241-1 2006 OBJECTIVE: To investigate whether FK506 (tacrolimus) can inhibit Fas- or A23187-induced interleukin (IL)-8 expression and cell death in A549 human alveolar epithelial cells, plus Fas-mediated acute lung injury in vivo. ammonium ferrous sulfate 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 88-106 16955241-1 2006 OBJECTIVE: To investigate whether FK506 (tacrolimus) can inhibit Fas- or A23187-induced interleukin (IL)-8 expression and cell death in A549 human alveolar epithelial cells, plus Fas-mediated acute lung injury in vivo. Calcimycin 73-79 C-X-C motif chemokine ligand 8 Homo sapiens 88-106 16687627-6 2006 Inhibition of these pathways with pyrrolidine dithiocarbamate, PD 98059, and fludarabine, respectively, attenuated GA-induced IL-8 secretion. pyrrolidine dithiocarbamic acid 34-61 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16750994-8 2006 The purinergic receptor antagonist suramin did block LL-37-induced ERK1/2 phosphorylation and IL-8 release, and expression of mRNA for the purinergic receptor P2X(7) was detected in HASM cells. Suramin 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16723453-7 2006 PD153035 reduced IL-8, AG1295 repressed IL-6, and both inhibitors partially downregulated VEGF production in UV-exposed PECs. 4-((3-bromophenyl)amino)-6,7-dimethoxyquinazoline 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 16687627-6 2006 Inhibition of these pathways with pyrrolidine dithiocarbamate, PD 98059, and fludarabine, respectively, attenuated GA-induced IL-8 secretion. fludarabine 77-88 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16723648-0 2006 Simvastatin decreases IL-6 and IL-8 production in epithelial cells. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 16687627-7 2006 Rosiglitazone dose-dependently attenuated GA-induced IL-8 and ICAM-1 signals in PTEC and completely abolished GA-induced STAT-1 signals but had no effect on NF-kappaB and MAPK activation. Rosiglitazone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 16723648-3 2006 Since oral epithelial cells participate importantly in periodontal inflammation, we measured simvastatin effects on interleukin-6 and interleukin-8 production by cultured human epithelial cell line (KB cells) in response to interleukin-1alpha. Simvastatin 93-104 C-X-C motif chemokine ligand 8 Homo sapiens 134-147 16702304-0 2006 Glutamine pretreatment reduces IL-8 production in human intestinal epithelial cells by limiting IkappaBalpha ubiquitination. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 16702304-3 2006 Because regulation of the inflammatory response was shown to be linked to proteolysis regulation, we hypothesized that glutamine pretreatment could act on IL-8 production in human intestinal epithelial cells through the regulation of inhibitor kappaB (IkappaB) ubiquitination. Glutamine 119-128 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 16702304-6 2006 A pretreatment with 10 mmol/L glutamine decreased IL-8 production under both basal and proinflammatory conditions (both P < 0.05). Glutamine 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 16845446-0 2006 Inhibitive effect of genistein on interleukin-8 expression in cultured human retinal pigment epithelial cells. Genistein 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 16783450-2 2006 The aim of this study was to explore the effects of 2 second-generation antihistamines, cetirizine and loratadine, on granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-8 (IL-8) secretions in human airway epithelial cells. Cetirizine 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 16783450-2 2006 The aim of this study was to explore the effects of 2 second-generation antihistamines, cetirizine and loratadine, on granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-8 (IL-8) secretions in human airway epithelial cells. Cetirizine 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 16783450-2 2006 The aim of this study was to explore the effects of 2 second-generation antihistamines, cetirizine and loratadine, on granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-8 (IL-8) secretions in human airway epithelial cells. Loratadine 103-113 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 16783450-2 2006 The aim of this study was to explore the effects of 2 second-generation antihistamines, cetirizine and loratadine, on granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukin-8 (IL-8) secretions in human airway epithelial cells. Loratadine 103-113 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 16783450-5 2006 Cetirizine (5, 10 microM) inhibited the production of IL-8 by 19% (p<0.05). Cetirizine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 16845446-4 2006 When the cells were treated with hypoxia (5% CO2, 95% N2), IL-8 secretion increased from 0.29 +/- 0.04 to 2.59 +/- 0.42 ng/ml. Nitrogen 54-56 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 16845446-5 2006 To study calcium-dependent IL-8 expression, cells were treated with KCl at 25 mM, norepinephrine (NE) at 10 nM, and glutamate (Glu) at 1 microM for 8 h. As a result, the levels of IL-8 protein in supernatants were significantly increased compared with that in the controls. Calcium 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 16845446-6 2006 When the cells are treated with genistein (50, 100, 200 microM) for 30 min before hypoxia or stimulations by KCl, NE, and Glu, the elevated expression of IL-8 protein was all suppressed in a concentration-dependent manner. Genistein 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 16845446-6 2006 When the cells are treated with genistein (50, 100, 200 microM) for 30 min before hypoxia or stimulations by KCl, NE, and Glu, the elevated expression of IL-8 protein was all suppressed in a concentration-dependent manner. Potassium Chloride 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 16815071-6 2006 TsAg induced maximal nuclear binding of p65, p50 and c-rel subunits of the transcriptional regulator NF-kappaB by 2 h. IkappaBalpha but not IkappaBbeta was degraded within 10 min before resynthesis by 2 h. Pre-treatment with the broad-spectrum NF-kappaB inhibitor pyrrolidine dithiocarbamate caused complete abrogation of TsAg-induced CCL2 secretion (p=0.005) and 91% reduction of CXCL8 secretion (p=0.0003). tsag 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 381-386 16845446-4 2006 When the cells were treated with hypoxia (5% CO2, 95% N2), IL-8 secretion increased from 0.29 +/- 0.04 to 2.59 +/- 0.42 ng/ml. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 16845446-6 2006 When the cells are treated with genistein (50, 100, 200 microM) for 30 min before hypoxia or stimulations by KCl, NE, and Glu, the elevated expression of IL-8 protein was all suppressed in a concentration-dependent manner. Glutamic Acid 122-125 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 16845446-2 2006 In this study, the effects of genistein on the expression of IL-8 in the arising retinal pigment epithelia-19 cells were studied. Genistein 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 16845446-7 2006 These results suggested that suppression of IL-8 expression in retinal pigment epithelial cells might partly account for the inhibitive effect of genistein on retinal neovascularization. Genistein 146-155 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 16740161-16 2006 Treatment with CpG increased phosphorylation of p38 and pretreatment with the p38 inhibitor SB202190 attenuated the synergistic increase in IL-8 protein levels. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 92-100 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 16787522-1 2006 It has been reported that urinary interleukin-6 (IL-6) and IL-8 levels are decreased in adult diabetic women with asymptomatic bacteriuria (ASB) when compared with non-diabetic women with ASB. asb 140-143 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 16787522-10 2006 Indeed, the IL-8 levels were higher in diabetic subjects with ASB as compared with those without it (70.0 vs. <3.1 pg/mg creatinine; p = 0.001), and there was a significant association between the urinary IL-8 concentration and the bacterial count (p = 0.001). asb 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 16787522-10 2006 Indeed, the IL-8 levels were higher in diabetic subjects with ASB as compared with those without it (70.0 vs. <3.1 pg/mg creatinine; p = 0.001), and there was a significant association between the urinary IL-8 concentration and the bacterial count (p = 0.001). asb 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 16787522-10 2006 Indeed, the IL-8 levels were higher in diabetic subjects with ASB as compared with those without it (70.0 vs. <3.1 pg/mg creatinine; p = 0.001), and there was a significant association between the urinary IL-8 concentration and the bacterial count (p = 0.001). Creatinine 124-134 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 16787522-11 2006 Diabetic patients with leukocyturia had higher IL-8 concentration than those without it (20.9 vs. <3.1 pg/mg creatinine; p = 0.003). Creatinine 112-122 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 16787522-15 2006 Our results suggest that diabetic children with ASB mount an IL-8 response to pathogens, which is comparable to non-diabetic children with bacteriuria. asb 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 16641218-4 2006 F2-isoprostane levels (a marker of oxidant injury) in tracheal aspirates were significantly higher in the cimetidine group at 4 d and at 10 d. There were no significant differences between the groups in tracheal aspirate levels of inflammatory markers (leukotriene B4, IL-8, and nucleated cell count) or arachidonic acid metabolites. Cimetidine 106-116 C-X-C motif chemokine ligand 8 Homo sapiens 269-273 16739069-5 2006 GTE significantly induced IL-8 mRNA expression, which was not mediated indirectly via an induction of IL-1beta mRNA expression. epigallocatechin gallate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 16739069-6 2006 EGCG only exerted a weak although significant induction of IL-8 mRNA expression at the highest concentration. epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 16739069-8 2006 GTE and EGCG significantly decreased secreted IL-8 concentrations. epigallocatechin gallate 8-12 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 16739069-10 2006 The IL-1beta-mediated increase of IL-8 secretion was significantly inhibited by GTE in a dose-dependent manner. epigallocatechin gallate 80-83 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 16427093-6 2006 Inhibition of the EGFR by either an anti-EGFR neutralizing antibody or by its specific inhibitor AG1478 (1 microM) blocked TNF-alpha-induced IL-8 secretion. RTKI cpd 97-103 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 16690053-1 2006 Human chymase induced release of interleukin-8 (IL-8) in human EoL-1 cells that had been differentiated into eosinophil-like cells with butyric acid. Butyric Acid 136-148 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 16690053-1 2006 Human chymase induced release of interleukin-8 (IL-8) in human EoL-1 cells that had been differentiated into eosinophil-like cells with butyric acid. Butyric Acid 136-148 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 16690053-4 2006 The chymase-induced IL-8 release was inhibited by pertussis toxin as well as U0126 (an inhibitor for extracellular signal-regulated kinase pathway) and SB203580 (p38 inhibitor), suggesting that the chymase-induced IL-8 production is mediated by G protein-coupled receptor and mitogen-activated protein kinases. U 0126 77-82 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 16690053-4 2006 The chymase-induced IL-8 release was inhibited by pertussis toxin as well as U0126 (an inhibitor for extracellular signal-regulated kinase pathway) and SB203580 (p38 inhibitor), suggesting that the chymase-induced IL-8 production is mediated by G protein-coupled receptor and mitogen-activated protein kinases. SB 203580 152-160 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 16690053-4 2006 The chymase-induced IL-8 release was inhibited by pertussis toxin as well as U0126 (an inhibitor for extracellular signal-regulated kinase pathway) and SB203580 (p38 inhibitor), suggesting that the chymase-induced IL-8 production is mediated by G protein-coupled receptor and mitogen-activated protein kinases. SB 203580 152-160 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 16764700-2 2006 The aim of the study is to analyse the expression of pro-inflammatory cytokines IL-1beta, TNF-alpha, IFN-gamma and the chemokine CXCL8 (IL-8) in liver tissue and their expression and secretion in PBMC of patients with chronic hepatitis C (CHC), in response to pentoxyfilline (PTX). Pentoxifylline 260-274 C-X-C motif chemokine ligand 8 Homo sapiens 129-134 16764700-2 2006 The aim of the study is to analyse the expression of pro-inflammatory cytokines IL-1beta, TNF-alpha, IFN-gamma and the chemokine CXCL8 (IL-8) in liver tissue and their expression and secretion in PBMC of patients with chronic hepatitis C (CHC), in response to pentoxyfilline (PTX). Pentoxifylline 260-274 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 16764700-2 2006 The aim of the study is to analyse the expression of pro-inflammatory cytokines IL-1beta, TNF-alpha, IFN-gamma and the chemokine CXCL8 (IL-8) in liver tissue and their expression and secretion in PBMC of patients with chronic hepatitis C (CHC), in response to pentoxyfilline (PTX). Pentoxifylline 276-279 C-X-C motif chemokine ligand 8 Homo sapiens 129-134 16764700-2 2006 The aim of the study is to analyse the expression of pro-inflammatory cytokines IL-1beta, TNF-alpha, IFN-gamma and the chemokine CXCL8 (IL-8) in liver tissue and their expression and secretion in PBMC of patients with chronic hepatitis C (CHC), in response to pentoxyfilline (PTX). Pentoxifylline 276-279 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 16764700-6 2006 Following PTX, PBMC exhibited a decrease in IFN-gamma mRNA 12.2 versus 1.5 molecules (P = 0.028) and CXCL8 4.2 versus 2.5 molecules (P = 0.027). Pentoxifylline 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 16388870-6 2006 Addition of p38 MAPK inhibitor, SB-203580 and NF-kappaB inhibitor Bay 11-7082, suppressed IBDV-induced NO production and mRNA expression of iNOS, IL-8 and COX-2. SB 203580 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 16388870-6 2006 Addition of p38 MAPK inhibitor, SB-203580 and NF-kappaB inhibitor Bay 11-7082, suppressed IBDV-induced NO production and mRNA expression of iNOS, IL-8 and COX-2. 3-(4-methylphenylsulfonyl)-2-propenenitrile 66-77 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 16427093-10 2006 Finally, both AR and IL-8 release-induced by TNF-alpha were eliminated by pretreatment with either GM6001, a broad-spectrum inhibitor for metalloprotease, or TAPI-1, relatively selective inhibitor for TNF-alpha converting enzyme (TACE). N-(2(R)-2-(hydroxamidocarbonylmethyl)-4-methylpentanoyl)-L-tryptophan methylamide 99-105 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 16707595-4 2006 EXPERIMENTAL DESIGN: The effects of dexamethasone on VEGF and IL-8 expression and cell proliferation were examined using DU145, which expresses glucocorticoid receptor. Dexamethasone 36-49 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 16707595-6 2006 RESULTS: Dexamethasone significantly down-regulated VEGF and IL-8 gene expression by 50% (P < 0.001) and 89% (P < 0.001), respectively, and decreased VEGF and IL-8 protein production by 55% (P < 0.001) and 74% (P < 0.001), respectively, under normoxic condition. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 16707595-6 2006 RESULTS: Dexamethasone significantly down-regulated VEGF and IL-8 gene expression by 50% (P < 0.001) and 89% (P < 0.001), respectively, and decreased VEGF and IL-8 protein production by 55% (P < 0.001) and 74% (P < 0.001), respectively, under normoxic condition. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 16707595-7 2006 Similarly, hydrocortisone down-regulated VEGF and IL-8 gene expression. Hydrocortisone 11-25 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 16707595-9 2006 Even under hypoxia-like conditions, dexamethasone inhibited VEGF and IL-8 expression. Dexamethasone 36-49 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 16376386-0 2006 Scoparone inhibits PMA-induced IL-8 and MCP-1 production through suppression of NF-kappaB activation in U937 cells. scoparone 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 16707595-10 2006 In DU145 xenografts, dexamethasone significantly decreased tumor volume and microvessel density and down-regulated VEGF and IL-8 gene expression, whereas dexamethasone did not affect the in vitro proliferation of the cells. Dexamethasone 21-34 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 16376386-0 2006 Scoparone inhibits PMA-induced IL-8 and MCP-1 production through suppression of NF-kappaB activation in U937 cells. Tetradecanoylphorbol Acetate 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 16353157-6 2006 We show that phenoxodiol inhibits hallmarks of endothelial cell activation, namely TNF or IL-1 induced E-selectin and VCAM-1 expression and IL-8 secretion. phenoxodiol 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 16424382-11 2006 Fluticasone alone reduced CCL5, CXCL8, and CXCL10 but had no effect on CXCL5. Fluticasone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 32-37 16373669-0 2006 Zn2+-induced IL-8 expression involves AP-1, JNK, and ERK activities in human airway epithelial cells. Zinc 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 16373669-3 2006 In this study, we examined the cellular mechanisms responsible for Zn(2+)-induced IL-8 expression. Zinc 67-69 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 16373669-4 2006 Zn(2+) stimulation resulted in pronounced increases in both IL-8 mRNA and protein expression in the human airway epithelial cell line (BEAS-2B). Zinc 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 16373669-5 2006 IL-8 promoter activity was significantly increased by Zn(2+) exposure in BEAS-2B cells, indicating that Zn(2+)-induced IL-8 expression is transcriptionally mediated. Zinc 54-56 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16376386-2 2006 In this study, the effects of scoparone on the expression of interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) and activation of nuclear factor-kappaB (NF-kappaB) were examined in U937 human monocytes activated with phorbol 12-myristate 13-acetate (PMA). scoparone 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 16376386-2 2006 In this study, the effects of scoparone on the expression of interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) and activation of nuclear factor-kappaB (NF-kappaB) were examined in U937 human monocytes activated with phorbol 12-myristate 13-acetate (PMA). scoparone 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 16376386-4 2006 Scoparone concentration-dependently reduced the release of IL-8 and MCP-1 protein and expression of IL-8 and MCP-1 mRNA levels induced by PMA. scoparone 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 16376386-4 2006 Scoparone concentration-dependently reduced the release of IL-8 and MCP-1 protein and expression of IL-8 and MCP-1 mRNA levels induced by PMA. scoparone 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 16373669-8 2006 We observed that Zn(2+) exposure induced the phosphorylation of ERK, JNK, and p38 MAPKs, whereas inhibition of ERK or JNK activity blocked IL-8 mRNA and protein expression in BEAS-2B cells treated with Zn(2+). Zinc 17-19 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 16373669-11 2006 These results suggested that Zn(2+)-induced inhibition of phosphatase activity is an initiating event in MAPK and AP-1 activation that leads to enhanced IL-8 expression by human airway epithelial cells. Zinc 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 16373669-5 2006 IL-8 promoter activity was significantly increased by Zn(2+) exposure in BEAS-2B cells, indicating that Zn(2+)-induced IL-8 expression is transcriptionally mediated. Zinc 54-56 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 16373669-5 2006 IL-8 promoter activity was significantly increased by Zn(2+) exposure in BEAS-2B cells, indicating that Zn(2+)-induced IL-8 expression is transcriptionally mediated. Zinc 104-106 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16421230-6 2006 When epithelial cells were incubated with polyinosine-polycytidylic acid and CpG oligodinucleotides, we observed dose-dependent upregulation of interleukin-8 secretion. polyinosine-polycytidylic acid 42-72 C-X-C motif chemokine ligand 8 Homo sapiens 144-157 16373669-5 2006 IL-8 promoter activity was significantly increased by Zn(2+) exposure in BEAS-2B cells, indicating that Zn(2+)-induced IL-8 expression is transcriptionally mediated. Zinc 104-106 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 16137694-7 2006 Rosiglitazone reduced the incremental area under the curves (dAUCs) for IL-6 (-63%, p<0.01) and IL-8 (-16%, p<0.05). Rosiglitazone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 16137694-9 2006 CONCLUSIONS: Rosiglitazone attenuated the postprandial increases of neutrophils, IL-6 and IL-8 in patients with type 2 diabetes. Rosiglitazone 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 16137694-12 2006 Rosiglitazone attenuated the postprandial increases of neutrophils, IL-6 and IL-8 in patients with type 2 diabetes. Rosiglitazone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 16631683-8 2006 Subgroup analysis revealed a significantly greater elevation in IL-6, IL-8, and IL-10 levels in PGF patients (all p < 0.01) versus PLTRE. Prostaglandins F 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 16631683-10 2006 CONCLUSIONS: Patients with PLTRE and PGF exhibited graded increases in IL-6, IL-8, and IL-10 concentrations. Prostaglandins F 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 16421230-6 2006 When epithelial cells were incubated with polyinosine-polycytidylic acid and CpG oligodinucleotides, we observed dose-dependent upregulation of interleukin-8 secretion. cpg oligodinucleotides 77-99 C-X-C motif chemokine ligand 8 Homo sapiens 144-157 16604541-8 2006 RESULTS: All oxysterols investigated are potent in vitro inducers of MCP-1, MIP-1beta, TNF-alpha, and/or IL-8 secretion, the latter involving the MEK/ERK1/2 cell signaling pathway. Oxysterols 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 16634798-10 2006 PD98059, an inhibitor of ERK phosphorylation, significantly reduced IgA AECA-stimulated endothelial IL-8. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 16675585-8 2006 RESULTS: Candesartan did not induce direct toxicity in KU-19-19 cells, but VEGF and interleukin-8 were significantly lower in candesartan-treated cells (2.55 +/- 0.25 and 6.58 +/- 0.48 pg/10(3) cells) than in the angiotensin II-treated control cells (3.16 +/- 0.42 and 7.91 +/- 0.69 pg/10(3) cells). candesartan 126-137 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 16670485-8 2006 In primary cultures, 17beta-estradiol caused a significant decrease of IL-6 and IL-8 gene expression, but had no effect on the levels of IL-1beta, MMP-2, and MMP-9 gene expression. Estradiol 21-37 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 16289596-10 2006 LPA induced significant migration and IL-8 secretion in DLD1, both of which were significantly inhibited by AG1478 or GM6001. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 16546701-2 2006 In this paper, we show that fludarabine can also induce pro-inflammatory stimulation of monocytic cells, as evaluated by increased expression of ICAM-1 and IL-8 release. fludarabine 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 16716121-6 2006 Pretreatment of HBECs with specific inhibitors against ERK 1/2 and JNK but not p38 could significantly inhibit nicotine-induced interleukin- 8 production. Nicotine 111-119 C-X-C motif chemokine ligand 8 Homo sapiens 128-142 16622236-7 2006 The IL-8 secretion in response to P. aeruginosa DNA was decreased by treatments that inhibit acidification of intracellular organelles, using chloroquine, a pH-neutralizing compound, or bafilomycin A1, an inhibitor of vacuolar H+-ATPase. Chloroquine 142-153 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 16622236-7 2006 The IL-8 secretion in response to P. aeruginosa DNA was decreased by treatments that inhibit acidification of intracellular organelles, using chloroquine, a pH-neutralizing compound, or bafilomycin A1, an inhibitor of vacuolar H+-ATPase. bafilomycin A1 186-200 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 16410784-4 2006 Addition of the hydrolysis-resistant ATP analogue, adenosine 5"-O-(3-thiotriphosphate) (ATPgammaS), to subconfluent cultures of the human microvascular endothelial cell-1 (HMEC-1) cell line led to a dose- and time-dependent increase in release of IL-6, IL-8, monocyte chemoattractant protein-1, and growth-regulated oncogene alpha. adenosine 5'-O-(3-thiotriphosphate) 51-86 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 16652423-6 2006 Stimulation of neutrophils with formyl-methionine-leucine-phenylalanine, IL-8, and LTB4 inhibited subsequent mobilization of calcium by the supernatant. Calcium 125-132 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 16289596-10 2006 LPA induced significant migration and IL-8 secretion in DLD1, both of which were significantly inhibited by AG1478 or GM6001. RTKI cpd 108-114 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 16289596-10 2006 LPA induced significant migration and IL-8 secretion in DLD1, both of which were significantly inhibited by AG1478 or GM6001. N-(2(R)-2-(hydroxamidocarbonylmethyl)-4-methylpentanoyl)-L-tryptophan methylamide 118-124 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 16406095-7 2006 Histamine and poly (I:C), a specific TLR3 ligand stimulated interleukin (IL)-8 secretion from both cell types. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 60-78 16641879-7 2006 RESULTS: There was a significant correlation between IL-8 concentration and AST, ALP, GGT, total bilirubin and albumin levels in blood serum. Bilirubin 97-106 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 16406095-7 2006 Histamine and poly (I:C), a specific TLR3 ligand stimulated interleukin (IL)-8 secretion from both cell types. Carbon 22-23 C-X-C motif chemokine ligand 8 Homo sapiens 60-78 16406095-8 2006 Moreover, histamine enhanced poly (I:C)-induced IL-8 secretion and phosphorylation of NF-kappaB in the two cell types, and histamine H1 receptor antagonists inhibited the action of histamine. Histamine 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 16406095-7 2006 Histamine and poly (I:C), a specific TLR3 ligand stimulated interleukin (IL)-8 secretion from both cell types. poly 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 60-78 16406095-8 2006 Moreover, histamine enhanced poly (I:C)-induced IL-8 secretion and phosphorylation of NF-kappaB in the two cell types, and histamine H1 receptor antagonists inhibited the action of histamine. Poly I-C 29-39 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 16406095-9 2006 In conclusion, histamine selectively up-regulated expression of TLR3, and stimulated IL-8 secretion from the cells. Histamine 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 16585276-11 2006 To avoid dilution effects, urinary levels of IL-8 were expressed as the ratio of cytokine-to-urinary creatinine. Creatinine 101-111 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 16406095-10 2006 Histamine also enhanced poly (I:C) induced IL-8 secretion and phosphorylation of NF-kappaB. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 16406095-10 2006 Histamine also enhanced poly (I:C) induced IL-8 secretion and phosphorylation of NF-kappaB. Poly I-C 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 16326104-0 2006 Sesquiterpene lactones as inhibitors of IL-8 expression in HeLa cells. sesquiterpene lactones 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 16529714-8 2006 SbS also inhibited IL-8 production, prevented IkappaB alpha degradation, and reduced both NF-kappaB-DNA binding and NF-kappaB reporter gene up-regulation in IL-1beta or LPS-stimulated THP-1 cells. sbs 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 16552751-8 2006 Pretreatment with BAPTA/AM or GF109203X also significantly attenuated ghrelin-induced IL-8 production. 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid 18-23 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 16552751-8 2006 Pretreatment with BAPTA/AM or GF109203X also significantly attenuated ghrelin-induced IL-8 production. bisindolylmaleimide I 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 16600024-8 2006 Phorbol myristate acetate-stimulated oxidative burst and IL-8 release by IL-1beta, lipopolysaccharide and GM-CSF in whole blood from mild but not severe asthmatics were inhibited after prednisolone. Tetradecanoylphorbol Acetate 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 16600024-8 2006 Phorbol myristate acetate-stimulated oxidative burst and IL-8 release by IL-1beta, lipopolysaccharide and GM-CSF in whole blood from mild but not severe asthmatics were inhibited after prednisolone. Prednisolone 185-197 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 16570973-0 2006 Raman spectra of ionic liquids: a simulation study of AlF3 and its mixtures with NaF. aluminum fluoride 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 16322472-5 2006 HNP-induced IL-8 release was inhibited by treatment with the nucleotide receptor antagonists suramin and reactive blue. Suramin 93-100 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 16570973-1 2006 Theoretical Raman spectra of the melts of NaF/AlF3 mixtures have been obtained from computer simulations in order to examine how the Raman spectra reflect the coordination structure around the Al3+ ions. ALUMINUM ION 193-197 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 16572448-8 2006 When hemoglobin, as a scavenger of carbon monoxide, was added to auranofin-treated synovial cell lines, LPS-dependent production of IL-6 and IL-8 was increased. Carbon Monoxide 35-50 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 16572448-8 2006 When hemoglobin, as a scavenger of carbon monoxide, was added to auranofin-treated synovial cell lines, LPS-dependent production of IL-6 and IL-8 was increased. Auranofin 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 16322472-5 2006 HNP-induced IL-8 release was inhibited by treatment with the nucleotide receptor antagonists suramin and reactive blue. reactive blue 105-118 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 16217757-8 2006 VEGF-induced IL-8 production at the mRNA (real time RT-PCR) and protein levels (ELISA) are also suppressed with EGCG. epigallocatechin gallate 112-116 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 16517565-0 2006 Effects of combined 17beta-estradiol with TCDD on secretion of chemokine IL-8 and expression of its receptor CXCR1 in endometriotic focus-associated cells in co-culture. Estradiol 20-36 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 16517565-0 2006 Effects of combined 17beta-estradiol with TCDD on secretion of chemokine IL-8 and expression of its receptor CXCR1 in endometriotic focus-associated cells in co-culture. Polychlorinated Dibenzodioxins 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 16517565-4 2006 The regulatory mechanisms of dioxin and estrogen in the expression of CXCR1/IL-8 in the corresponding cells will help in elucidating roles of the chemokine in the aetiology of endometriosis. Dioxins 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 16517565-8 2006 TCDD promoted IL-8 secretion by human pelvic mesothelial cells (HPMC), and 17beta-estradiol magnified the stimulatory effect. Polychlorinated Dibenzodioxins 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16202406-11 2006 SB202190, PD98059 and doxycycline markedly suppressed the levels of p-JNK-1/p-JNK-2 and/or p-ERK1/p-ERK2, as well as IL-1beta, TNF-alpha and IL-8 mRNAs and proteins stimulated by hyperosmolar media. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 16202406-11 2006 SB202190, PD98059 and doxycycline markedly suppressed the levels of p-JNK-1/p-JNK-2 and/or p-ERK1/p-ERK2, as well as IL-1beta, TNF-alpha and IL-8 mRNAs and proteins stimulated by hyperosmolar media. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 16202406-11 2006 SB202190, PD98059 and doxycycline markedly suppressed the levels of p-JNK-1/p-JNK-2 and/or p-ERK1/p-ERK2, as well as IL-1beta, TNF-alpha and IL-8 mRNAs and proteins stimulated by hyperosmolar media. Doxycycline 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 16517565-11 2006 Interaction of HPMC and the monocytes significantly stimulated IL-8 secretion, suggesting a main resource of IL-8 in peritoneal cavity with endometriosis. hydroxypropylmethylcellulose-lactose matrix 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 16517565-11 2006 Interaction of HPMC and the monocytes significantly stimulated IL-8 secretion, suggesting a main resource of IL-8 in peritoneal cavity with endometriosis. hydroxypropylmethylcellulose-lactose matrix 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 16517565-12 2006 TCDD promoted IL-8 secretion by HPMC-U937 co-culture, but exerted a contrary effect for IL-8 secretion when combined with estradiol. Polychlorinated Dibenzodioxins 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16517565-12 2006 TCDD promoted IL-8 secretion by HPMC-U937 co-culture, but exerted a contrary effect for IL-8 secretion when combined with estradiol. Polychlorinated Dibenzodioxins 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 16517565-12 2006 TCDD promoted IL-8 secretion by HPMC-U937 co-culture, but exerted a contrary effect for IL-8 secretion when combined with estradiol. hydroxypropylmethylcellulose-lactose matrix 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16517565-8 2006 TCDD promoted IL-8 secretion by human pelvic mesothelial cells (HPMC), and 17beta-estradiol magnified the stimulatory effect. hydroxypropylmethylcellulose-lactose matrix 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16517565-9 2006 Both 17beta-estradiol and TCDD alone inhibited IL-8 secretion of U937 (a cell line of monocyte), but combination of 17beta-estradiol and TCDD had no further inhibitory effect. Estradiol 5-21 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 16270354-7 2006 In turn, exposure of B-CLL cells to recombinant IL-8 significantly decreased spontaneous apoptosis as well as chlorambucil- and fludarabine-mediated cytoxicity in B-CLL cells. Chlorambucil 110-122 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 16517565-9 2006 Both 17beta-estradiol and TCDD alone inhibited IL-8 secretion of U937 (a cell line of monocyte), but combination of 17beta-estradiol and TCDD had no further inhibitory effect. Polychlorinated Dibenzodioxins 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 16517565-10 2006 The co-culture of endometrial stromal cells (ESC) with HPMC produced more IL-8 than respective or total production of either of the cells alone, and estradiol played a synergistic stimulatory role with TCDD in IL-8 secretion of the co-culture. hydroxypropylmethylcellulose-lactose matrix 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16517565-10 2006 The co-culture of endometrial stromal cells (ESC) with HPMC produced more IL-8 than respective or total production of either of the cells alone, and estradiol played a synergistic stimulatory role with TCDD in IL-8 secretion of the co-culture. hydroxypropylmethylcellulose-lactose matrix 55-59 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 16517565-10 2006 The co-culture of endometrial stromal cells (ESC) with HPMC produced more IL-8 than respective or total production of either of the cells alone, and estradiol played a synergistic stimulatory role with TCDD in IL-8 secretion of the co-culture. Estradiol 149-158 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 16517565-10 2006 The co-culture of endometrial stromal cells (ESC) with HPMC produced more IL-8 than respective or total production of either of the cells alone, and estradiol played a synergistic stimulatory role with TCDD in IL-8 secretion of the co-culture. Polychlorinated Dibenzodioxins 202-206 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 16392133-2 2006 We have previously reported that titanium particles stimulate the selective induction of interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1) chemokines in human osteoblast-like osteosarcoma cells. Titanium 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 16392133-2 2006 We have previously reported that titanium particles stimulate the selective induction of interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1) chemokines in human osteoblast-like osteosarcoma cells. Titanium 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 16392133-4 2006 We demonstrate that titanium particles result in enhanced IL-8 and MCP-1 protein secretion as well as differential chemokine gene activation. Titanium 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 16392133-8 2006 We also demonstrate that while cytochalasin D, a potent inhibitor of phagocytosis, suppressed the titanium particle effect on IL-8 protein release in human bone marrow-derived osteoblasts, the inhibitor had no effect on IL-8 expression in MG-63 osteoblast-like cells. Cytochalasin D 31-45 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16392133-8 2006 We also demonstrate that while cytochalasin D, a potent inhibitor of phagocytosis, suppressed the titanium particle effect on IL-8 protein release in human bone marrow-derived osteoblasts, the inhibitor had no effect on IL-8 expression in MG-63 osteoblast-like cells. Titanium 98-106 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16331685-0 2006 Cardiac glycoside inhibits IL-8-induced biological responses by downregulating IL-8 receptors through altering membrane fluidity. Glycosides 8-17 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 16331685-0 2006 Cardiac glycoside inhibits IL-8-induced biological responses by downregulating IL-8 receptors through altering membrane fluidity. Glycosides 8-17 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 16331685-2 2006 In this report we provide evidences that oleandrin, a cardiac glycoside potentially inhibited IL-8-, formyl peptide (FMLP)-, EGF-, or nerve growth factor (NGF)-, but not IL-1- or TNF-induced NF-kappaB activation in macrophages. oleandrin 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16331685-2 2006 In this report we provide evidences that oleandrin, a cardiac glycoside potentially inhibited IL-8-, formyl peptide (FMLP)-, EGF-, or nerve growth factor (NGF)-, but not IL-1- or TNF-induced NF-kappaB activation in macrophages. Glycosides 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16331685-3 2006 Oleandrin inhibited IL-8-, but not TNF-induced NF-kappaB-dependent genes expression. oleandrin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 16331685-4 2006 Oleandrin inhibited the binding of IL-8, EGF, or NGF, but not IL-1 or TNF. oleandrin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 16331685-7 2006 Phospholipids significantly protected oleandrin-mediated inhibition of IL-8 binding thereby restoring IL-8-induced NF-kappaB activation. Phospholipids 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 16270354-7 2006 In turn, exposure of B-CLL cells to recombinant IL-8 significantly decreased spontaneous apoptosis as well as chlorambucil- and fludarabine-mediated cytoxicity in B-CLL cells. fludarabine 128-139 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 16331685-7 2006 Phospholipids significantly protected oleandrin-mediated inhibition of IL-8 binding thereby restoring IL-8-induced NF-kappaB activation. Phospholipids 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 16331685-7 2006 Phospholipids significantly protected oleandrin-mediated inhibition of IL-8 binding thereby restoring IL-8-induced NF-kappaB activation. oleandrin 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 16331685-7 2006 Phospholipids significantly protected oleandrin-mediated inhibition of IL-8 binding thereby restoring IL-8-induced NF-kappaB activation. oleandrin 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 16549444-6 2006 Notably, the degree of inhibition of IL-8 release from HUVEC by HDL3 was correlated with the ability of HDL3 to promote cholesterol efflux (r = -0.80, P = 0.03). Cholesterol 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 16683673-0 2006 Evaluation of fluoride release from teeth after topical application of NaF, SnF2 and APF and antimicrobial activity on mutans streptococci. Fluorides 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 16683673-1 2006 UNLABELLED: The objectives of this study were to evaluate and compare the amount and pattern of fluoride release from teeth after topical application of 2% NaF, 8% SnF2 and 1.23% APF at different time intervals. Fluorides 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 16780654-6 2006 The expressions of TNF-alpha and IL-8 and their protein quantity in lung tissues significantly increased in LMV after ventilation compared to that in CMV and NMV (P < 0.01). lmv 108-111 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 16434099-5 2006 Furthermore, IL-8 induction could be blocked by brefeldin A, which inhibits ricin translocation into the cytosol. Brefeldin A 48-59 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 16434099-7 2006 Treatment of 28SC cells with the pyridylimidizole analogue SB203580, a known inhibitor of p38 MAPK, suppressed ricin-mediated IL-8 release. pyridylimidizole 33-49 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16434099-7 2006 Treatment of 28SC cells with the pyridylimidizole analogue SB203580, a known inhibitor of p38 MAPK, suppressed ricin-mediated IL-8 release. SB 203580 59-67 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16481221-5 2006 Hypoxia (1% O2) up-regulated vascular endothelial growth factor-A (VEGF-A) but, unexpectedly, it decreased interleukin-8 (IL-8) and placenta growth factor (PlGF) expression. Oxygen 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 16481221-6 2006 Atorvastatin (0.1-1 microM) attenuated PlGF in HMEC-1 in normoxia while it decreased VEGF-A and IL-8 production both in normoxia and hypoxia. Atorvastatin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 16497987-6 2006 These studies also demonstrated that pretreatment of EC with NOS inhibitor, Nomega-nitro-L-arginine-methyl ester (L-NAME), significantly inhibited Ox-PAPC-induced IL-8 synthesis. NG-Nitroarginine Methyl Ester 76-112 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 16497987-6 2006 These studies also demonstrated that pretreatment of EC with NOS inhibitor, Nomega-nitro-L-arginine-methyl ester (L-NAME), significantly inhibited Ox-PAPC-induced IL-8 synthesis. NG-Nitroarginine Methyl Ester 114-120 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 16331685-9 2006 Overall, our results suggest that oleandrin inhibits IL-8-mediated biological responses in diverse cell types by modulating IL-8Rs through altering membrane fluidity and microviscosity. oleandrin 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 16780654-6 2006 The expressions of TNF-alpha and IL-8 and their protein quantity in lung tissues significantly increased in LMV after ventilation compared to that in CMV and NMV (P < 0.01). nmv 158-161 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 16254130-5 2006 WBH induced an increase in human growth hormone (hGH), ACTH, and cortisol as well as in TNF-alpha, IL-6, IL-8, and IL-12R. wbh 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 16647268-0 2006 Increased NaCl-induced interleukin-8 production by human bronchial epithelial cells is enhanced by the DeltaF508/W1282X mutation of the cystic fibrosis transmembrane conductance regulator gene. Sodium Chloride 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 16647268-6 2006 Human bronchial epithelial cells with the DeltaF508/W1282X CFTR mutation produce an exaggerated amount of basal and NaCl-induced IL-8. Sodium Chloride 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 16479515-7 2006 CXCL-8 mRNA was superinduced by TNF- alpha in the presence of the protein-synthesis inhibitor cycloheximide. Cycloheximide 94-107 C-X-C motif chemokine ligand 8 Homo sapiens 0-6 16564702-12 2006 However, in endothelial cells stimulated with ATP, the released fraction was effective in attenuating IL-1beta activation of the IL-8 reporter. Adenosine Triphosphate 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 16553947-4 2006 Glucan phosphate-treated leukocytes induced a substantial amount of IL-8 (peak at 18 h: 5000 pg/ml), likely due to binding of NFkappaB to a consensus site in the IL-8 promoter. glucan phosphate 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 16553947-4 2006 Glucan phosphate-treated leukocytes induced a substantial amount of IL-8 (peak at 18 h: 5000 pg/ml), likely due to binding of NFkappaB to a consensus site in the IL-8 promoter. glucan phosphate 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 16553947-5 2006 An increase in IL-1receptor antagonist (RA) production (peak at 24 h: 12000 pg/ml) by glucan phosphate-treated cells positively correlated with IL-8 levels. glucan phosphate 86-102 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 16509590-6 2006 A collection of analytically defined lipolanthionine peptide amides exhibited an inhibitory effect of the TLR2-mediated IL-8 secretion when applied in high molar excess to the agonistic synthetic lipopeptide Pam3Cys-Ser-(Lys)4-OH. lipolanthionine peptide amides 37-67 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 16509590-6 2006 A collection of analytically defined lipolanthionine peptide amides exhibited an inhibitory effect of the TLR2-mediated IL-8 secretion when applied in high molar excess to the agonistic synthetic lipopeptide Pam3Cys-Ser-(Lys)4-OH. Lysine 221-225 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 16509590-6 2006 A collection of analytically defined lipolanthionine peptide amides exhibited an inhibitory effect of the TLR2-mediated IL-8 secretion when applied in high molar excess to the agonistic synthetic lipopeptide Pam3Cys-Ser-(Lys)4-OH. 4-oh 225-229 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 16623401-6 2006 RESULTS: For patients in the LFA group, production of IL-8 was significantly less increased at the end of the surgical procedure; however there was no significant difference in total production between groups. lfa 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 16249253-4 2006 High glucose also increased the specific binding of (125)I-labeled insulin in HAEC accompanied by accelerated production of interleukin (IL)-6 and IL-8. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 16527606-4 2006 IL-6 and IL-8 secretion was greater in coincubates of aCTL cells with 13-06-ISP and 13-06-CSP immunoselected cells than those with 13-06-MG parental cells. 13-06-isp 70-79 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 16385087-4 2006 METHODS AND RESULTS: Metformin dose-dependently inhibited IL-1beta-induced release of the pro-inflammatory cytokines IL-6 and IL-8 in ECs, SMCs, and Mphis. Metformin 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16521278-0 2006 Lipoteichoic acid (LTA) from Staphylococcus aureus stimulates human neutrophil cytokine release by a CD14-dependent, Toll-like-receptor-independent mechanism: Autocrine role of tumor necrosis factor-[alpha] in mediating LTA-induced interleukin-8 generation. lipoteichoic acid 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 232-245 16423909-6 2006 RESULTS: We found the following associations with plasma marker concentrations: Age, neutrophil count, and glucose concentration were positively associated with IL-8 concentrations in children and adults, as were smoking and platelet count in adults. Glucose 107-114 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 16505650-8 2006 MEASUREMENT AND MAIN RESULTS: Postoperative serum levels of both interleukin-6 and interleukin-8 increased significantly over baseline, but the peak levels observed 4 hrs postoperatively were significantly lower in the atorvastatin group. Atorvastatin 219-231 C-X-C motif chemokine ligand 8 Homo sapiens 83-96 16521278-0 2006 Lipoteichoic acid (LTA) from Staphylococcus aureus stimulates human neutrophil cytokine release by a CD14-dependent, Toll-like-receptor-independent mechanism: Autocrine role of tumor necrosis factor-[alpha] in mediating LTA-induced interleukin-8 generation. lipoteichoic acid 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 232-245 16428071-5 2006 Budesonide had a suppressive effect on both constitutive and LPS-induced IL-8 gene expression. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 16511915-0 2006 Simvastatin inhibits production of interleukin 6 (IL-6) and IL-8 and cell proliferation induced by tumor necrosis factor-alpha in fibroblast-like synoviocytes from patients with rheumatoid arthritis. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 16428068-12 2006 Moreover, NS-398 suppressed the anti-apoptotic activity of IL-8 and IL-1beta, but did not induce COX-2; therefore, the pro-apoptotic mechanism of the selective COX-2 inhibitor may be unrelated to COX-2 activity. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 16511915-3 2006 We investigated whether simvastatin could inhibit the expression of interleukin 6 (IL-6) and IL-8 and cell proliferation induced by tumor necrosis factor-alpha (TNF-alpha) in fibroblast-like synoviocytes (FLS) obtained from RA patients undergoing joint replacement therapy. Simvastatin 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 16511915-6 2006 RESULTS: Real-time PCR analysis revealed that the levels of IL-6 and IL-8 mRNA expressed by FLS were reduced by simvastatin in a dose-dependent manner. Simvastatin 112-123 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 16476030-5 2006 RESULTS: Following the dexamethasone treatment, the levels of TNF-alpha, IL-1-alpha, IL-6, and IL-8 were decreased significantly, and IL-1-alpha and IL-8 were detected at a level without a statistically significant difference from controls. Dexamethasone 23-36 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 16511915-7 2006 Levels of IL-6 and IL-8 in FLS culture supernatants were decreased by simvastatin in a time-dependent and dose-dependent manner. Simvastatin 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 16511915-9 2006 These effects of simvastatin on IL-6 and IL-8 production and cell proliferation were reversed in the presence of mevalonic acid or geranylgeranyl-pyrophosphate, but not with farnesyl-pyrophosphate. Simvastatin 17-28 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 16511915-9 2006 These effects of simvastatin on IL-6 and IL-8 production and cell proliferation were reversed in the presence of mevalonic acid or geranylgeranyl-pyrophosphate, but not with farnesyl-pyrophosphate. Mevalonic Acid 113-127 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 16511915-9 2006 These effects of simvastatin on IL-6 and IL-8 production and cell proliferation were reversed in the presence of mevalonic acid or geranylgeranyl-pyrophosphate, but not with farnesyl-pyrophosphate. geranylgeranyl pyrophosphate 131-159 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 16511915-10 2006 CONCLUSION: Our results suggest that the beneficial effect of simvastatin in RA patients may involve inhibition of IL-6 and IL-8 production, as well as reduction of cell proliferation. Simvastatin 62-73 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 16384711-6 2006 RESULTS: PMA and fMLP-induced neutrophil respiratory burst and chemotaxis were lower after 14 days of NAC intake but not after 2 h. In vitro incubation with NAC inhibited release of elastase (p < 0.05), IL-8 (p < 0.05), respiratory burst and NFkappaB activation at 10 mM but not at lower concentrations. Acetylcysteine 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 16465414-1 2006 We previously demonstrated the doxorubicin-induced expression of urokinase-type plasminogen activator (uPA), interleukin-8 (IL-8), monocyte chemoattractant protein-1 (MCP-1) and tumor necrosis factor-alpha in human RC-K8 lymphoma cells and NCI-H69 small cell lung carcinoma cells in which reactive oxygen species might be involved. Doxorubicin 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 109-122 16465414-1 2006 We previously demonstrated the doxorubicin-induced expression of urokinase-type plasminogen activator (uPA), interleukin-8 (IL-8), monocyte chemoattractant protein-1 (MCP-1) and tumor necrosis factor-alpha in human RC-K8 lymphoma cells and NCI-H69 small cell lung carcinoma cells in which reactive oxygen species might be involved. Doxorubicin 31-42 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 16384711-6 2006 RESULTS: PMA and fMLP-induced neutrophil respiratory burst and chemotaxis were lower after 14 days of NAC intake but not after 2 h. In vitro incubation with NAC inhibited release of elastase (p < 0.05), IL-8 (p < 0.05), respiratory burst and NFkappaB activation at 10 mM but not at lower concentrations. Acetylcysteine 157-160 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 16476030-5 2006 RESULTS: Following the dexamethasone treatment, the levels of TNF-alpha, IL-1-alpha, IL-6, and IL-8 were decreased significantly, and IL-1-alpha and IL-8 were detected at a level without a statistically significant difference from controls. Dexamethasone 23-36 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 16503719-7 2006 Atorvastatin significantly reduced the production of epithelial neutrophil-activating peptide-78, interleukin-6, interleukin-8, and monocyte chemotactic protein-1 (p<0.001 to p<0.05) in a concentration-dependent manner without affecting basal production of interleukin-10, fibroblast growth factor, and granulocyte colony stimulating factor. Atorvastatin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 16397875-5 2006 The mean values of IL-1beta, IL-8, and IL-10 at T4 were lower in the HFOV group than in the PSV + VG group. hfov 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 16300899-7 2006 Concomitantly, CRCHM elicited decrease in the catalytic adenylate cyclase (AC) activity (cAMP formation) in response to isoproterenol plus GTP or forskolin or NaF. crchm 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 159-162 16552354-6 2006 IL-8 secretions from ECs and PMNs were higher with 300 and 600 micromol/L than with 1000 micromol/L GLN, and this was consistent with the expression of the IL-8 receptor on PMNs. Glutamine 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16552354-6 2006 IL-8 secretions from ECs and PMNs were higher with 300 and 600 micromol/L than with 1000 micromol/L GLN, and this was consistent with the expression of the IL-8 receptor on PMNs. Glutamine 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 16552354-11 2006 GLN administration at levels similar to or higher than physiological concentrations reduced IL-8 and adhesion molecule expression, and PMN transmigration was also decreased after stimulation with plasma or PDF from a surgical patient. Glutamine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 16483201-1 2006 Rotationally resolved infrared spectra are reported for the binary complexes of HCN and LiF, LiCl, NaF, and NaCl, formed in helium nanodroplets. Helium 124-130 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 16448181-3 2006 The inhibition of H2O2-induced IL-8 secretion from Caco-2 cells was observed by pretreatment for 2 h with PPPs, but not with phosvitin. Hydrogen Peroxide 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 16197369-0 2006 Transcriptional regulation of lysophosphatidic acid-induced interleukin-8 expression and secretion by p38 MAPK and JNK in human bronchial epithelial cells. lysophosphatidic acid 30-51 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 16197369-3 2006 We have recently demonstrated that LPA (lysophosphatidic acid) stimulated IL-8 production in HBEpCs via protein kinase C delta dependent signal transduction. lysophosphatidic acid 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16197369-3 2006 We have recently demonstrated that LPA (lysophosphatidic acid) stimulated IL-8 production in HBEpCs via protein kinase C delta dependent signal transduction. lysophosphatidic acid 40-61 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16197369-6 2006 Exposure of HBEpCs to LPA (1 microM) enhanced expression and secretion of IL-8 by 5-8-fold and stimulated threonine/tyrosine phosphorylation of ERK (extracellular-signal-regulated kinase), p38 MAPK and JNK (c-Jun N-terminal kinase). lysophosphatidic acid 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16197369-7 2006 The LPA-induced secretion of IL-8 was blocked by the p38 MAPK inhibitor SB203580, by p38 MAPK siRNA (small interfering RNA), and by the JNK inhibitor JNK(i) II, but not by the MEK (MAPK/ERK kinase) inhibitor, PD98059. lysophosphatidic acid 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 16499573-10 2006 We also observed that throughout C. trachomatis persistence induced by doxycycline (Dox) treatment, IL-1beta, IL-6, IL-8 and TNF-alpha expression was reduced, whereas the synthesis of IL-10 and IL-12p70 remained unchanged but not sustained. Doxycycline 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 16451045-3 2006 We investigated the effects of NaF, NaCl, NaBr, and NaI on the molecular organization of H2O by a calorimetric methodology developed by us earlier. Water 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 16197369-7 2006 The LPA-induced secretion of IL-8 was blocked by the p38 MAPK inhibitor SB203580, by p38 MAPK siRNA (small interfering RNA), and by the JNK inhibitor JNK(i) II, but not by the MEK (MAPK/ERK kinase) inhibitor, PD98059. SB 203580 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 16197369-7 2006 The LPA-induced secretion of IL-8 was blocked by the p38 MAPK inhibitor SB203580, by p38 MAPK siRNA (small interfering RNA), and by the JNK inhibitor JNK(i) II, but not by the MEK (MAPK/ERK kinase) inhibitor, PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 209-216 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 16197369-9 2006 Furthermore, SB203580 attenuated LPA-dependent phosphorylation of IkappaB (inhibitory kappaB), NF-kappaB and phospho-p38 translocation to the nucleus, NF-kappaB transcription and IL-8 promoter-mediated luciferase reporter activity, without affecting the JNK pathway and AP-1 transcription. SB 203580 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 16197369-9 2006 Furthermore, SB203580 attenuated LPA-dependent phosphorylation of IkappaB (inhibitory kappaB), NF-kappaB and phospho-p38 translocation to the nucleus, NF-kappaB transcription and IL-8 promoter-mediated luciferase reporter activity, without affecting the JNK pathway and AP-1 transcription. lysophosphatidic acid 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 16197369-10 2006 Similarly, JNK(i) II only blocked LPA-mediated phosphorylation of JNK and c-Jun, AP-1 transcription and IL-8 promoter-mediated luciferase reporter activity, without blocking p38 MAPK-dependent NF-kappaB transcription. lysophosphatidic acid 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 16197369-11 2006 Additionally, siRNA for LPA(1-3) receptors partially blocked LPA-induced IL-8 production and activation of MAPKs. lysophosphatidic acid 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 16197369-12 2006 The LPA1 and LPA3 receptors, as compared with LPA2, were most efficient in transducing LPA-mediated IL-8 production. lysophosphatidic acid 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 16197369-13 2006 These results show an independent role for p38 MAPK and JNK in LPA-induced IL-8 expression and secretion via NF-kappaB and AP-1 transcription respectively in HBEpCs. lysophosphatidic acid 63-66 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 16300899-7 2006 Concomitantly, CRCHM elicited decrease in the catalytic adenylate cyclase (AC) activity (cAMP formation) in response to isoproterenol plus GTP or forskolin or NaF. Cyclic AMP 89-93 C-X-C motif chemokine ligand 8 Homo sapiens 159-162 16269456-14 2006 Adrenal-secreted IL-8 is one point of convergence between the adrenal gland and the immune system and may have relevance in physiological and pathophysiological conditions associated with increased levels of aldosterone secretagogues and the immune system. Aldosterone 208-219 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 16447232-8 2006 Finally, CQ-resistant CEM cells displayed a markedly reduced capacity to release proinflammatory cytokines (tumor necrosis factor alpha) and chemokines (interleukin-8). Chloroquine 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 153-166 16265667-6 2006 Furthermore, our studies on the intracellular signaling pathways reveal that poly(I:C) stimulation activates IkappaB kinase (IKK), extracellular signal-regulated kinase (ERK), and c-Jun N-terminal kinase (JNK) in CRT-MG. Pharmacological inhibitors of nuclear factor-kappaB (NF-kappaB), JNK, ERK, glycogen synthase kinase-3beta (GSK-3beta), and dsRNA-activated protein kinase (PKR) inhibit the expression of IL-8 and IP-10 in astrocytes, indicating that the activation of these signaling molecules is required for the TLR3-mediated chemokine gene induction. Poly I-C 77-86 C-X-C motif chemokine ligand 8 Homo sapiens 407-411 16352735-0 2006 Anti-inflammatory effects of moxifloxacin on IL-8, IL-1beta and TNF-alpha secretion and NFkappaB and MAP-kinase activation in human monocytes stimulated with Aspergillus fumigatus. Moxifloxacin 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 16373365-6 2006 Results from reverse transcription-PCR and flow cytometry analysis of HUTEC indicate that the interaction with Daudi cells induce an increased expression of IL-6 and IL-8 mRNA and cell-surface expression of intercellular adhesion molecule-1, all of which were prevented by sodium salicylate, an inhibitor of NF-kappaB activation. Sodium Salicylate 273-290 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 16455619-5 2006 Prior treatment with PGE(2) (1 microM) produced 86 and 80% decreases in GM-CSF and IL-8 release, respectively. Dinoprostone 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 16384605-9 2006 Magnesium sulfate dose dependently inhibited the endotoxin-stimulated IL-8 production in both decidual and amniotic cells. Magnesium Sulfate 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 16384605-11 2006 In conclusion, magnesium sulfate differentially suppresses endotoxin-stimulated IL-8 production in amniotic and decidual cells in vitro. Magnesium Sulfate 15-32 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 16467702-7 2006 RESULTS: There were statistically significant improvements in SNOT-20 score, nasal endoscopy, saccharine transit time, and IL-8 levels in lavage fluid (P<.05) in the macrolide group. Macrolides 169-178 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 16455619-6 2006 Similarly, the cAMP analogue, 8-bromo-cAMP (8Br-cAMP) and the phosphodiesterase-4 (PDE(4)) inhibitor, rolipram, also repressed GM-CSF and IL-8 release. Cyclic AMP 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 16455619-6 2006 Similarly, the cAMP analogue, 8-bromo-cAMP (8Br-cAMP) and the phosphodiesterase-4 (PDE(4)) inhibitor, rolipram, also repressed GM-CSF and IL-8 release. 8-Bromo Cyclic Adenosine Monophosphate 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 16249194-11 2006 In the in vitro studies, the average value for cell-associated IL-6 and IL-8 was higher in CKD (155+/-95 pg/ml monocytes for IL-6 and 722+/-921 pg/ml monocytes for IL-8) vs HS (137+/-87 pg/ml monocytes and 186+/-125 pg/ml monocytes) (P<0.01) and was not affected by simvastatin alone. Simvastatin 269-280 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16455619-6 2006 Similarly, the cAMP analogue, 8-bromo-cAMP (8Br-cAMP) and the phosphodiesterase-4 (PDE(4)) inhibitor, rolipram, also repressed GM-CSF and IL-8 release. 8-Bromo Cyclic Adenosine Monophosphate 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 16455619-6 2006 Similarly, the cAMP analogue, 8-bromo-cAMP (8Br-cAMP) and the phosphodiesterase-4 (PDE(4)) inhibitor, rolipram, also repressed GM-CSF and IL-8 release. Rolipram 102-110 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 16278684-4 2006 Treatment with SB-216763 increased expression of cyclooxygenase-2 (COX-2) and IL-8, which are downstream targets of ERK1/2 activation; this induction was abolished by MEK/ERK inhibition, suggesting GSK-3 inhibition induced COX-2 and IL-8 through ERK1/2 activation. SB 216763 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 16393986-8 2006 In addition, PTX-B inhibited the secretion of IL-6-induced, AP-1-dependent genes, including urokinase-type plasminogen activator, CXCL8/IL-8, and CCL2/monocyte chemotactic protein-1. pumiliotoxin B 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 130-135 16393986-8 2006 In addition, PTX-B inhibited the secretion of IL-6-induced, AP-1-dependent genes, including urokinase-type plasminogen activator, CXCL8/IL-8, and CCL2/monocyte chemotactic protein-1. pumiliotoxin B 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 16183151-27 2006 Homocysteine mediated expression and secretion of monocyte chemoattractant protein-1 and interleukin-8 in human monocytes. Homocysteine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 16388589-4 2006 Their stabilities depend significantly upon the presence of salt: strongly for NaCl but less so for NaF, demonstrating specific interactions with chloride ions. Salts 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 16388589-4 2006 Their stabilities depend significantly upon the presence of salt: strongly for NaCl but less so for NaF, demonstrating specific interactions with chloride ions. Chlorides 146-154 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 16388589-7 2006 A comparison of the effects of NaCl/KCl with NaF showed that homeodomain binding results in a release not only of cations from the DNA phosphates but also of chloride ions specifically associated with the proteins. Sodium Chloride 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 16388589-7 2006 A comparison of the effects of NaCl/KCl with NaF showed that homeodomain binding results in a release not only of cations from the DNA phosphates but also of chloride ions specifically associated with the proteins. Phosphates 135-145 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 16388589-7 2006 A comparison of the effects of NaCl/KCl with NaF showed that homeodomain binding results in a release not only of cations from the DNA phosphates but also of chloride ions specifically associated with the proteins. Chlorides 158-166 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 16394009-0 2006 Activation of TLR-9 induces IL-8 secretion through peroxynitrite signaling in human neutrophils. Peroxynitrous Acid 51-64 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 16394009-3 2006 Recent studies indicate that peroxynitrite (ONOO-) may function as an intracellular signal for the production of IL-8, one of the key regulators of leukocyte trafficking in inflammation. Peroxynitrous Acid 29-42 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 16394009-3 2006 Recent studies indicate that peroxynitrite (ONOO-) may function as an intracellular signal for the production of IL-8, one of the key regulators of leukocyte trafficking in inflammation. oxido nitrite 44-49 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 16394009-8 2006 CpG-DNA-induced IL-8 mRNA expression and release was also blocked by the NO synthase inhibitor Nomega-nitro-L-arginine methyl ester. NG-Nitroarginine Methyl Ester 95-131 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 16394009-11 2006 These results identify ONOO- -dependent activation of NF-kappaB and c-Fos as an important mechanism that mediates PMN responses, including IL-8 gene expression and release, to bacterial DNA and unmethylated CpG motifs in particular. onoo 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 16278684-4 2006 Treatment with SB-216763 increased expression of cyclooxygenase-2 (COX-2) and IL-8, which are downstream targets of ERK1/2 activation; this induction was abolished by MEK/ERK inhibition, suggesting GSK-3 inhibition induced COX-2 and IL-8 through ERK1/2 activation. SB 216763 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 16278684-5 2006 The transcriptional induction of COX-2 and IL-8 by GSK-3 inhibition was further demonstrated by the increased COX-2 and IL-8 promoter activity after SB-216763 treatment or transfection with GSK-3alpha or GSK-3beta siRNA. SB 216763 149-158 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 16278684-5 2006 The transcriptional induction of COX-2 and IL-8 by GSK-3 inhibition was further demonstrated by the increased COX-2 and IL-8 promoter activity after SB-216763 treatment or transfection with GSK-3alpha or GSK-3beta siRNA. SB 216763 149-158 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 16364007-8 2006 DEX treatment reduced IL-8 levels in control and LPS-treated cultures by 70-90%. Dextromethorphan 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 16671497-6 2006 RESULTS: HUVECs cultured at glucose concentrations of 300 and 400 mg/dL produced more (p < 0.01) IL-8 than control cells (200 mg/dL). Glucose 28-35 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 16671497-7 2006 HUVECs cultured at glucose concentrations of 300 and 400 mg/dL also produced more (p < 0.01) IL-8 than those cultured in the absence of LPS. Glucose 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 16085674-0 2006 Macrolide antibiotics modulate ERK phosphorylation and IL-8 and GM-CSF production by human bronchial epithelial cells. macrolide antibiotics 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 16085674-4 2006 CAM decreased IL-8 over the first 6 h and then significantly increased interleukin (IL)-8 at 12-72 h after exposure (P < 0.0001). Clarithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16085674-4 2006 CAM decreased IL-8 over the first 6 h and then significantly increased interleukin (IL)-8 at 12-72 h after exposure (P < 0.0001). Clarithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 71-89 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Azithromycin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Clarithromycin 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Clarithromycin 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Azithromycin 153-156 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Azithromycin 153-156 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Azithromycin 153-156 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Clarithromycin 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Clarithromycin 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 16085674-5 2006 AZM also increased IL-8 at 24 and 48 h, and CAM increased granulocyte-macrophage colony-stimulating factor at 48 h. In the presence of LPS, both CAM and AZM dose-dependently increased IL-8 secretion over 24 h, but after 5 days of exposure to 10 microg/ml CAM there is suppression of IL-8 (P < 0.001). Clarithromycin 145-148 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 16085674-6 2006 PD-98059, an inhibitor of MAP kinase/ERK kinase, inhibited CAM-induced IL-8 (P < 0.0001) and GM-CSF (P < 0.01) release. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 16085674-7 2006 The p38 MAP kinase inhibitor SB-203580 increased CAM-induced IL-8 release (P < 0.001), and the c-jun NH2-terminal kinase inhibitor SP-600125 had no effect on IL-8. SB 203580 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 16085674-7 2006 The p38 MAP kinase inhibitor SB-203580 increased CAM-induced IL-8 release (P < 0.001), and the c-jun NH2-terminal kinase inhibitor SP-600125 had no effect on IL-8. Clarithromycin 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 16085674-11 2006 The p38 MAP kinase inhibitor, SB-203580 increased ERK phosphorylation and IL-8 secretion. SB 203580 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16803639-6 2006 RGD-targeted adenovirus delivered the dnIkappaB via alphavbeta3 to become functionally expressed, leading to complete abolishment of TNF-alpha-induced up-regulation of E-selectin, ICAM-1, VCAM-1, IL-6, IL-8, VEGF-A and Tie-2. dnikappab 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 17002793-9 2006 These cytokines have previously been shown to independently regulate the frequency (IFN-gamma) and amplitude (IL-8) of the oscillations of key metabolites in neutrophils, including nicotinamide adenine dinucleotide (phosphate) (NAD(P)H) and superoxide ion. NAD 181-214 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 17002793-9 2006 These cytokines have previously been shown to independently regulate the frequency (IFN-gamma) and amplitude (IL-8) of the oscillations of key metabolites in neutrophils, including nicotinamide adenine dinucleotide (phosphate) (NAD(P)H) and superoxide ion. Phosphates 216-225 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 17002793-9 2006 These cytokines have previously been shown to independently regulate the frequency (IFN-gamma) and amplitude (IL-8) of the oscillations of key metabolites in neutrophils, including nicotinamide adenine dinucleotide (phosphate) (NAD(P)H) and superoxide ion. Superoxides 241-251 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 17469513-11 2006 ATP content was reduced with rising concentrations of NaF: by 74.6% at 20 tmol/L; by 75.5% at 100 micromol/L; by 90.8% at 200 imol/L; and by 99.9% at 10(5) micromol/L. Adenosine Triphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 16924333-5 2006 Mouse lymphoma and human fibroblast cells were exposed to sodium fluoride (NaF) at final concentration ranging from 7 to 100 microg/mL for 3 h at 37 degrees C. The results pointed out that NaF in all tested concentrations did not contribute to DNA damage as depicted by the mean tail moment and tail intensity for both cellular types assessed. Sodium Fluoride 58-73 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 17100619-9 2006 In human monocytic cells, both MDP and DMPs exhibited definite activities; marked synergistic interleukin (IL)-8 secretion was induced by DMPs and MDP in combination with synthetic TLR agonists, and suppression of the mRNA expressions of NOD1 and NOD2, respectively, by RNA interference specifically inhibited synergistic IL-8 secretion. Unithiol 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 94-112 16253565-4 2006 Incubation with poly(I:C) significantly enhanced the secretion of RANTES and IL-8. poly 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 16253565-6 2006 The JNK inhibitor SP600125 and the PI3-kinase inhibitor LY294002 significantly blocked the poly(I:C)-induced release of RANTES and IL-8, whereas the p38 MAP kinase inhibitor SB203580 suppressed poly(I:C)-induced secretion of IL-8, but not RANTES. pyrazolanthrone 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 16253565-6 2006 The JNK inhibitor SP600125 and the PI3-kinase inhibitor LY294002 significantly blocked the poly(I:C)-induced release of RANTES and IL-8, whereas the p38 MAP kinase inhibitor SB203580 suppressed poly(I:C)-induced secretion of IL-8, but not RANTES. pyrazolanthrone 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 16253565-6 2006 The JNK inhibitor SP600125 and the PI3-kinase inhibitor LY294002 significantly blocked the poly(I:C)-induced release of RANTES and IL-8, whereas the p38 MAP kinase inhibitor SB203580 suppressed poly(I:C)-induced secretion of IL-8, but not RANTES. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 16253565-6 2006 The JNK inhibitor SP600125 and the PI3-kinase inhibitor LY294002 significantly blocked the poly(I:C)-induced release of RANTES and IL-8, whereas the p38 MAP kinase inhibitor SB203580 suppressed poly(I:C)-induced secretion of IL-8, but not RANTES. SB 203580 174-182 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 16963197-7 2006 Cytologic evaluation was performed on Papanicolaou-stained cytospin preparations of NAF. papanicolaou 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 17945891-7 2006 Our simulation results identify TGF-beta, IL-8 and IL-13 as the intervention points which are consistent with known clinical results to prevent DHF from occurring. dhf 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 17100619-9 2006 In human monocytic cells, both MDP and DMPs exhibited definite activities; marked synergistic interleukin (IL)-8 secretion was induced by DMPs and MDP in combination with synthetic TLR agonists, and suppression of the mRNA expressions of NOD1 and NOD2, respectively, by RNA interference specifically inhibited synergistic IL-8 secretion. Unithiol 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 322-326 17100619-9 2006 In human monocytic cells, both MDP and DMPs exhibited definite activities; marked synergistic interleukin (IL)-8 secretion was induced by DMPs and MDP in combination with synthetic TLR agonists, and suppression of the mRNA expressions of NOD1 and NOD2, respectively, by RNA interference specifically inhibited synergistic IL-8 secretion. Unithiol 138-142 C-X-C motif chemokine ligand 8 Homo sapiens 94-112 16433036-3 2006 Centrifugal force enhanced the cytotoxicity of sodium fluoride (NaF), but not that of redox compounds (hydrogen peroxide, sodium ascorbate, gallic acid) or chemotherapeutic agents (daunorubicin, doxorubicin, idarubicin, mitoxantrone, peplomycin, 5-FU). Sodium Fluoride 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 16387930-1 2006 Clarithromycin (CM) has been found to inhibit the production of the intercellular adhesion molecule (ICAM)-1 and the secretion of interleukin (IL)-6 and IL-8, which may have beneficial effects on the pathophysiological changes related to rhinovirus (RV) infection. Clarithromycin 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 16387930-1 2006 Clarithromycin (CM) has been found to inhibit the production of the intercellular adhesion molecule (ICAM)-1 and the secretion of interleukin (IL)-6 and IL-8, which may have beneficial effects on the pathophysiological changes related to rhinovirus (RV) infection. Clarithromycin 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 17974146-8 2006 The elevated IL-8 level in PBMCs of CRF reflect the imbalance of Thl/Th2 ratio and subsequent impairment of cellular immunity in those patients. Orlistat 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 17974147-2 2006 Chronic elevated glucose level in DM increases monocyte adhesion to aortic endothelial cells (ECs) which is mediated primarily through induction of interleukin-8 (IL-8). Glucose 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 17974147-2 2006 Chronic elevated glucose level in DM increases monocyte adhesion to aortic endothelial cells (ECs) which is mediated primarily through induction of interleukin-8 (IL-8). Glucose 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 16423036-3 2006 Stimulation of HCECs with the TLR3 agonist poly(I:C) induced the activation of nuclear factor (NF)-kappaB and production of the proinflammatory cytokine interleukin (IL)-6 and the chemokine IL-8. Poly I 43-49 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 16423036-3 2006 Stimulation of HCECs with the TLR3 agonist poly(I:C) induced the activation of nuclear factor (NF)-kappaB and production of the proinflammatory cytokine interleukin (IL)-6 and the chemokine IL-8. Carbon 50-52 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 16491014-8 2006 Ro-31-8220, a PKC inhibitor, and PD98059, a mitogen-activated protein/ERK kinase inhibitor, suppressed the histamine-induced ERK activation and the production of granulocyte macrophage colony-stimulating factor and IL-8. Ro 31-8220 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 16491014-0 2006 Histamine H1 receptor-stimulated interleukin 8 and granulocyte macrophage colony-stimulating factor production by bronchial epithelial cells requires extracellular signal-regulated kinase signaling via protein kinase C. BACKGROUND: Histamine stimulates the release of several cytokines, such as interleukin (IL)-8 and granulocyte macrophage colony-stimulating factor, from bronchial epithelial cells. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 295-313 16491014-8 2006 Ro-31-8220, a PKC inhibitor, and PD98059, a mitogen-activated protein/ERK kinase inhibitor, suppressed the histamine-induced ERK activation and the production of granulocyte macrophage colony-stimulating factor and IL-8. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 16491014-8 2006 Ro-31-8220, a PKC inhibitor, and PD98059, a mitogen-activated protein/ERK kinase inhibitor, suppressed the histamine-induced ERK activation and the production of granulocyte macrophage colony-stimulating factor and IL-8. Histamine 107-116 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 16491014-11 2006 Histamine also augmented the IL-8 production caused by IL-4 or tumor necrosis factor-alpha. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 16741367-7 2006 RESULTS: Desloratadine and loratadine inhibited the constitutive and IFN-gamma-induced release of CCL5, CXCL8 and CXCL10 from keratinocytes, while the low release of CCL17 remained unchanged. desloratadine 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 104-109 16697690-6 2006 It was also found that PD98059, a mitogen-activated protein kinase (MAPK) pathway inhibitor and U0126, an inhibitor of extracellular signal-regulated kinase (ERK) blocks thrombin-induced phosphorylation of ERK1/2 and IL-8 secretion, indicating the involvement of MAPK/ERK signaling pathway in thrombin-induced IL-8 secretion. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 16697690-6 2006 It was also found that PD98059, a mitogen-activated protein kinase (MAPK) pathway inhibitor and U0126, an inhibitor of extracellular signal-regulated kinase (ERK) blocks thrombin-induced phosphorylation of ERK1/2 and IL-8 secretion, indicating the involvement of MAPK/ERK signaling pathway in thrombin-induced IL-8 secretion. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 310-314 16697690-6 2006 It was also found that PD98059, a mitogen-activated protein kinase (MAPK) pathway inhibitor and U0126, an inhibitor of extracellular signal-regulated kinase (ERK) blocks thrombin-induced phosphorylation of ERK1/2 and IL-8 secretion, indicating the involvement of MAPK/ERK signaling pathway in thrombin-induced IL-8 secretion. U 0126 96-101 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 16697690-6 2006 It was also found that PD98059, a mitogen-activated protein kinase (MAPK) pathway inhibitor and U0126, an inhibitor of extracellular signal-regulated kinase (ERK) blocks thrombin-induced phosphorylation of ERK1/2 and IL-8 secretion, indicating the involvement of MAPK/ERK signaling pathway in thrombin-induced IL-8 secretion. U 0126 96-101 C-X-C motif chemokine ligand 8 Homo sapiens 310-314 16697690-7 2006 p38 MAPK pathway appears also being involved as SB203580, a selective inhibitor of p38 MAPK inhibit phosphorylation of p38 MAPK and thrombin-induced IL-8 secretion. SB 203580 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 16741367-7 2006 RESULTS: Desloratadine and loratadine inhibited the constitutive and IFN-gamma-induced release of CCL5, CXCL8 and CXCL10 from keratinocytes, while the low release of CCL17 remained unchanged. Loratadine 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 104-109 16940740-0 2006 Prostaglandin D2 induces IL-8 and GM-CSF by bronchial epithelial cells in a CRTH2-independent pathway. Prostaglandin D2 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 16772726-1 2006 BACKGROUND: In our previous study, oligodeoxynucleotides containing unmethylated CpG motifs (CpG ODNs) significantly prolonged eosinophil survival without inducing active release of eosinophil-derived neurotoxin or interleukin 8. Oligodeoxyribonucleotides 35-56 C-X-C motif chemokine ligand 8 Homo sapiens 215-228 17131711-13 2006 The fluoride uptake seen in the cycling model correlated with a standard FDA EFU procedure for the NaF dentifrices. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 16897233-0 2006 Effects of sivelestat, a new elastase inhibitor, on IL-8 and MCP-1 production from stimulated human alveolar epithelial type II cells. sivelestat 11-21 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 17131712-12 2006 A re-hardening study, in which a series of the new toothpaste-base formulations containing increasing concentrations of NaF were evaluated, showed a clear fluoride dose response. Fluorides 155-163 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 17131711-8 2006 SMH for a 1450 ppm NaF test dentifrice was greater than for Elmex Sensitive (1450 ppm amine F) and placebo at 10 days, while both products were greater than the placebo at 20 days. N-(2-Ethoxyethyl)-N-{(2s)-2-Hydroxy-3-[(2r)-6-Hydroxy-4-Oxo-3,4-Dihydro-1'h-Spiro[chromene-2,3'-Piperidin]-1'-Yl]propyl}-2,6-Dimethylbenzenesulfonamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 17131711-10 2006 The fluoride uptake seen in the cycling model correlated for the NaF dentifrices with a standard EFU procedure. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 16490927-7 2006 The PKC stimulator, phorbol myristate acetate (PMA), strongly up-regulated CD93 expression on the cell surface of all three cell-lines and induced interleukin-8 (IL-8) production by the U937 cells and interferon-gamma (IFN-gamma) production by the KHYG-1 cells. Tetradecanoylphorbol Acetate 20-45 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 16332510-6 2006 Results showed that nicotine suppressed the LPS induced production of IL-6 and IL-8 in both cell lines. Nicotine 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 16365062-0 2006 Soy isoflavones alter expression of genes associated with cancer progression, including interleukin-8, in androgen-independent PC-3 human prostate cancer cells. Isoflavones 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 16490927-7 2006 The PKC stimulator, phorbol myristate acetate (PMA), strongly up-regulated CD93 expression on the cell surface of all three cell-lines and induced interleukin-8 (IL-8) production by the U937 cells and interferon-gamma (IFN-gamma) production by the KHYG-1 cells. Tetradecanoylphorbol Acetate 20-45 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 16490927-7 2006 The PKC stimulator, phorbol myristate acetate (PMA), strongly up-regulated CD93 expression on the cell surface of all three cell-lines and induced interleukin-8 (IL-8) production by the U937 cells and interferon-gamma (IFN-gamma) production by the KHYG-1 cells. Tetradecanoylphorbol Acetate 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 16490927-7 2006 The PKC stimulator, phorbol myristate acetate (PMA), strongly up-regulated CD93 expression on the cell surface of all three cell-lines and induced interleukin-8 (IL-8) production by the U937 cells and interferon-gamma (IFN-gamma) production by the KHYG-1 cells. Tetradecanoylphorbol Acetate 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 16490927-8 2006 In addition, both Go6976 and Rottlerin inhibited the up-regulation of CD93 expression induced by PMA and IL-8 or IFN-gamma production in the respective cell-lines. Go 6976 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 16490927-8 2006 In addition, both Go6976 and Rottlerin inhibited the up-regulation of CD93 expression induced by PMA and IL-8 or IFN-gamma production in the respective cell-lines. rottlerin 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 16391493-0 2006 Effect of berberine on interleukin 8 and monocyte chemotactic protein 1 expression in a human retinal pigment epithelial cell line. Berberine 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 16391493-1 2006 PURPOSE: The aims of this study were to examine the effects of berberine, an alkaloid isolated from some medicinal herbs, on interleukin 8 (IL-8) and monocyte chemotactic protein 1 (MCP-1) expression in a human retinal pigment epithelial cell line (ARPE-19) stimulated with interleukin 1beta (IL-1beta) or tumor necrosis factor alpha (TNF-alpha). Berberine 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 125-138 16391493-1 2006 PURPOSE: The aims of this study were to examine the effects of berberine, an alkaloid isolated from some medicinal herbs, on interleukin 8 (IL-8) and monocyte chemotactic protein 1 (MCP-1) expression in a human retinal pigment epithelial cell line (ARPE-19) stimulated with interleukin 1beta (IL-1beta) or tumor necrosis factor alpha (TNF-alpha). Berberine 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 16391493-7 2006 CONCLUSION: These findings indicate that berberine dose-dependently inhibited the expression of IL-8 and MCP-1 induced by IL-1beta or TNF-alpha. Berberine 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 16497101-10 2006 Chemokine pathway (IL-8) and TNF-alpha activity seem to be modulated by Goeckerman"s therapy (polycyclic aromatic hydrocarbons). Polycyclic Aromatic Hydrocarbons 94-126 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 16129464-4 2006 Two hirsutinolides were studied for their NF-kappaB DNA binding activity in HaCaT cells (a human cell line similar to keratinocytes) and for their inhibition on IL-8 production in HeLa cells. hirsutinolides 4-18 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 16084120-6 2006 GM-CSF and IL-8 release by stimulated HBECs was also downregulated by ciclesonide (p < 0.05). ciclesonide 70-81 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 16543969-5 2006 17beta-dihydroequilenin and 17beta-estradiol at a concentration of 1 microM reduced IL-1alpha-induced up regulation of IL-6, IL-8 and MCP-1 close to control levels. 17-dihydroequilenin 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 16543969-5 2006 17beta-dihydroequilenin and 17beta-estradiol at a concentration of 1 microM reduced IL-1alpha-induced up regulation of IL-6, IL-8 and MCP-1 close to control levels. Estradiol 28-44 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 16554988-4 2006 CONCLUSION: Sivelestat sodium suppressed the production of PMN elastase and IL-8, resulting in improved respiratory function in patients with ALI caused by CPB. Sivelestat sodium 12-29 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 16543969-8 2006 The effect of 17beta-dihydroequilenin on IL-1alpha-induced production of IL-6, IL-8 and MCP-1 was reversed by the estrogen receptor antagonist ICI 182,780. 17-dihydroequilenin 14-37 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 16303327-5 2005 Subsequently, various concentrations of cis-9,trans-11-CLA vs. linoleic acid (LA, cis-9,cis-12-octadecadienoic acid) were tested for the effect on proliferative response and release of the pro-inflammatory cytokine IL-8 in stimulated BEAS-2B. Linoleic Acid 82-115 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 16646301-7 2006 In response to cigarette smoke lung epithelium may release TNF-alpha, TGF-beta, IL-1beta, GM-CSF, IL-8 reactive oxygen species (ROS). Reactive Oxygen Species 103-126 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 16303327-6 2005 Addition of cis-9,trans-11-CLA attenuated cell growth and significantly reduced IL-8 production at mRNA and protein levels. cis-9, trans-11-conjugated linoleic acid 12-30 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 16303327-8 2005 It was demonstrated that the inhibitory effect of cis-9,trans-11-CLA on IL-8 production is mediated through activation of the nuclear receptor PPARgamma, since blocking the receptor with a selective antagonist (GW9662) restored the stimulus-induced enhancement in IL-8 mRNA expression and protein secretion. cis-9 50-55 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16303327-8 2005 It was demonstrated that the inhibitory effect of cis-9,trans-11-CLA on IL-8 production is mediated through activation of the nuclear receptor PPARgamma, since blocking the receptor with a selective antagonist (GW9662) restored the stimulus-induced enhancement in IL-8 mRNA expression and protein secretion. cis-9 50-55 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 16303327-8 2005 It was demonstrated that the inhibitory effect of cis-9,trans-11-CLA on IL-8 production is mediated through activation of the nuclear receptor PPARgamma, since blocking the receptor with a selective antagonist (GW9662) restored the stimulus-induced enhancement in IL-8 mRNA expression and protein secretion. trans-11-cla 56-68 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16303327-8 2005 It was demonstrated that the inhibitory effect of cis-9,trans-11-CLA on IL-8 production is mediated through activation of the nuclear receptor PPARgamma, since blocking the receptor with a selective antagonist (GW9662) restored the stimulus-induced enhancement in IL-8 mRNA expression and protein secretion. trans-11-cla 56-68 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 16303327-8 2005 It was demonstrated that the inhibitory effect of cis-9,trans-11-CLA on IL-8 production is mediated through activation of the nuclear receptor PPARgamma, since blocking the receptor with a selective antagonist (GW9662) restored the stimulus-induced enhancement in IL-8 mRNA expression and protein secretion. 2-chloro-5-nitrobenzanilide 211-217 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 16303327-8 2005 It was demonstrated that the inhibitory effect of cis-9,trans-11-CLA on IL-8 production is mediated through activation of the nuclear receptor PPARgamma, since blocking the receptor with a selective antagonist (GW9662) restored the stimulus-induced enhancement in IL-8 mRNA expression and protein secretion. 2-chloro-5-nitrobenzanilide 211-217 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 16343928-3 2005 Increase of intracellular Ca(2+) resulted in inducing IL-8 gene expression and protein secretion, and addition of EGTA or BAPTA/AM before Ca(2+) stimulation inhibited the induction of IL-8 production. Egtazic Acid 114-118 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 16269654-7 2005 The inhibitory effect of adiponectin on TNF-alpha-induced IL-8 synthesis was inhibited by pretreatment with Rp-cAMP, a PKA inhibitor. Cyclic AMP 111-115 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 16269654-10 2005 The inhibitory effect of adiponectin on TNF-alpha-induced IL-8 synthesis was abrogated in part by pretreatment with the PI3 kinase inhibitor LY294002 or by Akt siRNA transfection, suggesting that Akt activation might inhibit IL-8 synthesis induced by TNF-alpha. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 141-149 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 16269654-10 2005 The inhibitory effect of adiponectin on TNF-alpha-induced IL-8 synthesis was abrogated in part by pretreatment with the PI3 kinase inhibitor LY294002 or by Akt siRNA transfection, suggesting that Akt activation might inhibit IL-8 synthesis induced by TNF-alpha. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 141-149 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 16343928-3 2005 Increase of intracellular Ca(2+) resulted in inducing IL-8 gene expression and protein secretion, and addition of EGTA or BAPTA/AM before Ca(2+) stimulation inhibited the induction of IL-8 production. 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid 122-127 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 16343928-5 2005 Pretreatment of MAPK inhibitors (PD98059 and SB203580) markedly blocked Ca(2+)-induced IL-8 production from cells, and anti-inflammatory drugs, such as dexamethasone and cyclosporin A, partially inhibited the activation of ERK1/2. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 16343928-5 2005 Pretreatment of MAPK inhibitors (PD98059 and SB203580) markedly blocked Ca(2+)-induced IL-8 production from cells, and anti-inflammatory drugs, such as dexamethasone and cyclosporin A, partially inhibited the activation of ERK1/2. SB 203580 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 16109883-6 2005 Moreover, UDP-glc increased secretion of the potent neutrophil chemoattractant CXCL8/IL-8 in A549 and BEAS-2B cells in a pertussis toxin-sensitive manner. Uridine Diphosphate Glucose 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 16266385-6 2005 A single dose of nasal budesonide caused a decrease in symptoms (P < 0.05) and nasal eosinophils (P < 0.05) with selective abrogation of IL-5 and IL-13 responses (P < 0.05), but a lack of effect on levels of eotaxin, RANTES, IL-8 and MCP-1. Budesonide 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 16109883-6 2005 Moreover, UDP-glc increased secretion of the potent neutrophil chemoattractant CXCL8/IL-8 in A549 and BEAS-2B cells in a pertussis toxin-sensitive manner. Uridine Diphosphate Glucose 10-17 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 16109883-7 2005 Moreover, reverse transcription and quantitative polymerase chain reaction revealed that UDP-glc modulated mRNA levels of IL-8/CXCL8. Uridine Diphosphate Glucose 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 16109883-7 2005 Moreover, reverse transcription and quantitative polymerase chain reaction revealed that UDP-glc modulated mRNA levels of IL-8/CXCL8. Uridine Diphosphate Glucose 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 127-132 16236565-4 2005 We have done several experiments using the rat ulnar loading model that demonstrate that (1) high-resolution [18F]NaF PET can detect newly created microdamage in vivo; (2) the microdamage detected in this way is co-localized with damage detected by histological and autoradiographic procedures; and (3) high-resolution [18F]NaF PET can distinguish between the effects of mechanical loading that does not produce damage and fatigue loading that creates microdamage. Fluorine-18 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 114-117 16040184-6 2005 Under stimulated conditions, arginine decreased IL-8 and Mig mRNA level (57% and 39%, for 0.1 vs. 2 mmol/l l-arginine, P<0.05, respectively), and production (respectively, 28 and 23%, both P<0.05). Arginine 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 16040184-9 2005 Use of NG-Methyl-l-arginine acetate, a NOS inhibitor which prevents arginine-induced NO production, suppressed the arginine-induced IL-8 inhibition (P<0.05). Methylarginine 7-35 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 16040184-9 2005 Use of NG-Methyl-l-arginine acetate, a NOS inhibitor which prevents arginine-induced NO production, suppressed the arginine-induced IL-8 inhibition (P<0.05). Arginine 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 16040184-9 2005 Use of NG-Methyl-l-arginine acetate, a NOS inhibitor which prevents arginine-induced NO production, suppressed the arginine-induced IL-8 inhibition (P<0.05). Arginine 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 16040184-10 2005 In HCT-8 cells, arginine enhanced cytokine-induced NO production, reduced IL-8 and Mig production and mRNA level and had no effects on other assessed chemokines. Arginine 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16040184-11 2005 In conclusion, arginine-induced IL-8 inhibition in HCT-8 cells involves NO pathway under inflammatory conditions. Arginine 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 16263754-5 2005 Moreover, inhibitors of MAPK (U0126 and SB203580) significantly reduced the IL-8 production, while the inhibition of NF-kappaB (pyrrolidinedithiocarbamate and retrovirus containing dominant-negative IkappaB alpha plasmid) did not affect the IL-8 expression increased by CpG ODN. U 0126 30-35 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 16263754-0 2005 CpG oligodeoxynucleotides induce IL-8 expression in CD34+ cells via mitogen-activated protein kinase-dependent and NF-kappaB-independent pathways. Oligodeoxyribonucleotides 4-25 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 16263754-5 2005 Moreover, inhibitors of MAPK (U0126 and SB203580) significantly reduced the IL-8 production, while the inhibition of NF-kappaB (pyrrolidinedithiocarbamate and retrovirus containing dominant-negative IkappaB alpha plasmid) did not affect the IL-8 expression increased by CpG ODN. SB 203580 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 17086498-0 2005 Combined effect of 25-hydroxycholesterol and IL-1beta on IL-8 production in human colon carcinoma cell line (Caco-2). 25-hydroxycholesterol 19-40 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 17086498-5 2005 Pre-treatment of Caco-2 cells with 25-hydroxycholesterol significantly enhanced IL-1beta-induced IL-8 expression at both mRNA and protein levels. 25-hydroxycholesterol 35-56 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 17086498-7 2005 Furthermore, pre-treatment with 25-hydroxycholesterol, followed by IL-1beta stimulation, enhanced IL-8 promoter activity beyond that observed with IL-1beta alone. 25-hydroxycholesterol 32-53 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 17086498-8 2005 These results suggest that 25-hydroxycholesterol enhances IL-1beta-induced IL-8 production, possibly by enhancing promoter activity. 25-hydroxycholesterol 27-48 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 16337471-6 2005 The production of IL-8 and monocyte chemoattractant protein 1 in response to either IgE alone or IgE and anti-IgE was enhanced by preincubation of the cells in IL-4 and was inhibited by preincubation of the cells with dexamethasone. Dexamethasone 218-231 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 16273203-0 2005 Vesnarinone inhibits angiogenesis and tumorigenicity of human oral squamous cell carcinoma cells by suppressing the expression of vascular endothelial growth factor and interleukin-8. vesnarinone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 16273203-7 2005 These findings suggest that vesnarinone can suppress the angiogenesis and growth of oral squamous cell carcinoma cells by inhibiting the expression of VEGF and IL-8 involved in blockade of NF-kappaB activity. vesnarinone 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 16819095-7 2005 In the present study we determined whether ozone exposure enhances DEP effect on interleukin-8 (IL-8) gene expression in human airway epithelial cells. Ozone 43-48 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 16819095-7 2005 In the present study we determined whether ozone exposure enhances DEP effect on interleukin-8 (IL-8) gene expression in human airway epithelial cells. Ozone 43-48 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 16819095-9 2005 The increased DEP-induced IL-8 gene expression following ozone exposure was attributed to ozone-induced increase in the activity of the transcription factors NF-kappaB and NF-IL6. Ozone 57-62 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 16354411-7 2005 Dexamethasone (100 nM) not only inhibited PGE2, PGF(2alpha), IL-6 and IL-8 production but also strongly suppressed the expression of COX-2 mRNA and protein. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 16123309-7 2005 Treatment of TNF-alpha-stimulated HT29 cells with EGCG dose-dependently inhibited the synthesis of IL-8, MIP-3alpha, and PGE2. epigallocatechin gallate 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 16123309-8 2005 Treatment with EGCG also inhibited the production of IL-8 and MIP-3alpha in TNF-alpha-stimulated T84 cells. epigallocatechin gallate 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 16224818-4 2005 Recombinant MIF counter-regulated in a dose-dependent fashion dexamethasone inhibition of TNF and IL-8 production by RAW 264.7 macrophages and U-937 promonocytes stimulated with lipopolysaccharides (LPS) or with LPS plus phorbol 12-myristate 13-acetate. Dexamethasone 62-75 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 16306601-10 2005 Treatment with the HDAC inhibitor trichostatin A blocks attenuation of IL-8 transcription. trichostatin A 34-48 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 16373705-0 2005 AP23846, a novel and highly potent Src family kinase inhibitor, reduces vascular endothelial growth factor and interleukin-8 expression in human solid tumor cell lines and abrogates downstream angiogenic processes. AP23846 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 15893939-4 2005 (AAR)IL-8 could be easily purified by one-step SP-Sepharose fast flow column after the lysate of recombinant bacterial cells was heated at 70 degrees C for 10 min. sp-sepharose 47-59 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 17292102-10 2005 In contrast, MWCNT-induced IL-8 release was reduced when exposed to 1% or 5% Pluronic F127 (P < .05). mwcnt 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 16229003-5 2005 LTB(4) and IL-8 in EBC were analyzed by specific enzyme immunoassay kits (EIA). NSC638702 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 16229003-12 2005 Our data suggest that EBC is suitable for evaluating neutrophil inflammatory mediators (LTB(4), IL-8, and pH) involved in the response to pulmonary bacterial colonization in CF children. NSC638702 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 18404520-3 2005 The aim of our study was to investigate the mechanism responsible for the priming effect of extracellular nucleotides on reactive oxygen species (ROS) production induced in human neutrophils by two different chemoattractants: formyl-methionyl-leucyl-phenylalanine (fMLP) and interleukin-8 (IL-8). Reactive Oxygen Species 121-144 C-X-C motif chemokine ligand 8 Homo sapiens 275-288 15946834-5 2005 The budesonide-treated subjects had significant reductions in IL-8 levels in the BAL after therapy (mean+/-sem, 1.53+/-0.72 at baseline vs. 0.70+/-0.48 ng/ml at 6 months, P=0.004) and a reduction in the mean percentages of neutrophils (17.16+/-2.67% vs. 13.25+/-2.28% P=0.002). Budesonide 4-14 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 15946834-7 2005 In stable patients with COPD, treatment with inhaled budesonide for a period of 6 months has a positive effect on markers of lung inflammation, as assessed by reduction in percentage neutrophils and IL-8 concentration in BAL. Budesonide 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 18404520-3 2005 The aim of our study was to investigate the mechanism responsible for the priming effect of extracellular nucleotides on reactive oxygen species (ROS) production induced in human neutrophils by two different chemoattractants: formyl-methionyl-leucyl-phenylalanine (fMLP) and interleukin-8 (IL-8). Reactive Oxygen Species 121-144 C-X-C motif chemokine ligand 8 Homo sapiens 290-294 18404520-3 2005 The aim of our study was to investigate the mechanism responsible for the priming effect of extracellular nucleotides on reactive oxygen species (ROS) production induced in human neutrophils by two different chemoattractants: formyl-methionyl-leucyl-phenylalanine (fMLP) and interleukin-8 (IL-8). Reactive Oxygen Species 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 275-288 18404520-3 2005 The aim of our study was to investigate the mechanism responsible for the priming effect of extracellular nucleotides on reactive oxygen species (ROS) production induced in human neutrophils by two different chemoattractants: formyl-methionyl-leucyl-phenylalanine (fMLP) and interleukin-8 (IL-8). Reactive Oxygen Species 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 290-294 16226369-4 2005 Addition of NaF, forskolin or sodium nitroprusside, activators of the inositol phosphates (IPs), cAMP and cGMP pathways, significantly increased their respective messengers in villous explants but failed to affect the hPL and hCG releases from syncytiotrophoblast. Inositol Phosphates 70-89 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 16494031-4 2005 RESULT: Compared with the control group, the levels of EGF, TGF-alpha, IL-1beta, IL-6 and IL-8 were significantly increased by treatment with Aloe coarse polysaccharide (P < 0.05, P < 0.01) and in a dose dependent manner, and the levels of TGF-beta1 and TNF were also increased but no statistical significance. Polysaccharides 154-168 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 16494031-5 2005 CONCLUSION: Aloe coarse polysaccharide may promote keratinocytes to secrete EGF, TGF-alpha, IL-1beta, IL-6 and IL-8. Polysaccharides 24-38 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 16325749-0 2005 Linoleic acid, but not oleic acid, upregulates production of interleukin-8 by human vascular smooth muscle cells via arachidonic acid metabolites under conditions of oxidative stress. Linoleic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 16325749-0 2005 Linoleic acid, but not oleic acid, upregulates production of interleukin-8 by human vascular smooth muscle cells via arachidonic acid metabolites under conditions of oxidative stress. Oleic Acid 3-13 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 16325749-0 2005 Linoleic acid, but not oleic acid, upregulates production of interleukin-8 by human vascular smooth muscle cells via arachidonic acid metabolites under conditions of oxidative stress. Arachidonic Acid 117-133 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 16325749-2 2005 We hypothesized that increased levels of LA under conditions of oxidative stress would increased production of IL-8 by vascular smooth muscle cells because LA is the dietary precursor to arachidonic acid (AA) and its metabolites that mediate inflammation. Arachidonic Acid 187-203 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 16325749-7 2005 RESULTS: Exposure of cells to OxLA, but not to OxOA, significantly increased production of IL-8. oxla 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 16325749-9 2005 Nordihydroguaiaretic acid, an inhibitor of the lipoxygenase pathway, blocked IL-8 and leukotriene B4 (LTB4) production induced by OxLA, whereas indomethacin, an inhibitor of the cyclooxygenase pathway, blocked IL-8, prostaglandin E2 (PGE2), and thromboxane B2 (TXB2) production. Masoprocol 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 16325749-9 2005 Nordihydroguaiaretic acid, an inhibitor of the lipoxygenase pathway, blocked IL-8 and leukotriene B4 (LTB4) production induced by OxLA, whereas indomethacin, an inhibitor of the cyclooxygenase pathway, blocked IL-8, prostaglandin E2 (PGE2), and thromboxane B2 (TXB2) production. Masoprocol 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 16325749-9 2005 Nordihydroguaiaretic acid, an inhibitor of the lipoxygenase pathway, blocked IL-8 and leukotriene B4 (LTB4) production induced by OxLA, whereas indomethacin, an inhibitor of the cyclooxygenase pathway, blocked IL-8, prostaglandin E2 (PGE2), and thromboxane B2 (TXB2) production. oxla 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 16325749-9 2005 Nordihydroguaiaretic acid, an inhibitor of the lipoxygenase pathway, blocked IL-8 and leukotriene B4 (LTB4) production induced by OxLA, whereas indomethacin, an inhibitor of the cyclooxygenase pathway, blocked IL-8, prostaglandin E2 (PGE2), and thromboxane B2 (TXB2) production. oxla 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 16226369-4 2005 Addition of NaF, forskolin or sodium nitroprusside, activators of the inositol phosphates (IPs), cAMP and cGMP pathways, significantly increased their respective messengers in villous explants but failed to affect the hPL and hCG releases from syncytiotrophoblast. Inositol Phosphates 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 16226369-4 2005 Addition of NaF, forskolin or sodium nitroprusside, activators of the inositol phosphates (IPs), cAMP and cGMP pathways, significantly increased their respective messengers in villous explants but failed to affect the hPL and hCG releases from syncytiotrophoblast. Cyclic AMP 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 16226369-4 2005 Addition of NaF, forskolin or sodium nitroprusside, activators of the inositol phosphates (IPs), cAMP and cGMP pathways, significantly increased their respective messengers in villous explants but failed to affect the hPL and hCG releases from syncytiotrophoblast. Cyclic GMP 106-110 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 16262287-4 2005 A (PAH-Naf)(n) film possesses a water contact angle of around 105 degrees, whereas the contact angle of a (PAH-Naf)(4)-(PAH-PAA)(m) multilayer is around 50 degrees. Water 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 7-10 16272305-3 2005 Estradiol inhibited the IL-1beta-mediated mRNA expression and secretion of human beta-defensin-2 and CXCL8 by uterine epithelial cells while progesterone had no effect. Estradiol 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 16277535-1 2005 In situ infrared visible sum frequency generation spectroscopy (SFG) is used to examine the structure of water at the Ag-water interface in NaF and KF electrolyte solutions. Water 105-110 C-X-C motif chemokine ligand 8 Homo sapiens 140-143 16181613-9 2005 RT-PCR results showed that honokiol suppressed NF-kappaB-regulated inflammatory and carcinogenic gene products including MMP-9, TNF-alpha, IL-8, ICAM-1 and MCP-1. honokiol 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 16262287-4 2005 A (PAH-Naf)(n) film possesses a water contact angle of around 105 degrees, whereas the contact angle of a (PAH-Naf)(4)-(PAH-PAA)(m) multilayer is around 50 degrees. pah-paa 120-127 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 16251427-8 2005 After 24 hours, enzyme-linked immunosorbent assay measurements indicated that thrombin (0.1 to 2.5 U/ml) elicited a dose-dependent elevation in secreted IL-8 (P<0.05) with 2.5 U/ml of thrombin increasing IL-8 levels by >14-fold in E2 and E2+medroxyprogesterone incubations. Medroxyprogesterone 247-266 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 16115878-4 2005 Here we showed that within 3 min, IL-8 treatment enhanced the Btk- and ERK1/2-dependent phosphorylation of p47(phox), as well as the recruitment of flavocytochrome b(558), p47(phox), and Rac2 into cholesterol-enriched detergent-resistant microdomains (or lipid rafts). Cholesterol 197-208 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 16115878-6 2005 Moreover, methyl-beta-cyclodextrin, which disrupts lipid rafts, inhibited IL-8-induced priming in response to fMLP. methyl-beta-cyclodextrin 10-34 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16212625-7 2005 IL1-beta stimulated IL-8 production was significantly increased in rapidly growing hTBEC cultures (n = 8) treated with cyclosporin (p = 0.049). Cyclosporine 119-130 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 16212625-9 2005 Inhibition of hTBEC growth, stimulation of IL-8 production and long-term effects on mucociliary phenotype and intact multi-layered epithelium suggest that cyclosporin may have a direct toxic effect on airway epithelium after transplantation. Cyclosporine 155-166 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 15987794-3 2005 METHODS AND RESULTS: The authors developed a double transgenic mouse model with doxycycline induced human IL-8 expression restricted to intestinal epithelial cells. Doxycycline 80-91 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 16276481-3 2005 Accordingly, pro-inflammatory agonists and oxygen radicals induce IL-8. Reactive Oxygen Species 43-58 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 16214039-10 2005 Sublethal superoxide dose evoked: (1) proinflammatory state manifested by increased IL-8 mRNA expression and CAM on the endothelial surface, (2) HUVEC apoptosis and activated endothelial NADPH oxidase, (3) increase in intracellular tissue factor, and (4) decrease in eNOS mRNA and protein and up-regulation of iNOS mRNA. Superoxides 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 16220077-5 2005 C-reactive protein could augment the production of reactive oxygen species (ROS) as measured by chemiluminescence and inhibitors of NAD(P)H oxidase (DPI and PAO) and ROS scavengers (superoxide dismutase, catalase, and 1% dimethyl sulphoxide) abolished C-reactive protein-induced IL-8 secretion. Reactive Oxygen Species 51-74 C-X-C motif chemokine ligand 8 Homo sapiens 279-283 16220077-5 2005 C-reactive protein could augment the production of reactive oxygen species (ROS) as measured by chemiluminescence and inhibitors of NAD(P)H oxidase (DPI and PAO) and ROS scavengers (superoxide dismutase, catalase, and 1% dimethyl sulphoxide) abolished C-reactive protein-induced IL-8 secretion. Reactive Oxygen Species 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 279-283 16220077-7 2005 The inhibitors of ERK 1/2 (PD98059), p38 (SB203580) MAPK, and NF-kappaB (PDTC and MG132) significantly decreased C-reactive protein-induced IL-8 secretion in human monocytes. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 16220077-7 2005 The inhibitors of ERK 1/2 (PD98059), p38 (SB203580) MAPK, and NF-kappaB (PDTC and MG132) significantly decreased C-reactive protein-induced IL-8 secretion in human monocytes. SB 203580 42-50 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 16118056-4 2005 Addition of budesonide to the apical side of Caco-2 cells, decreased both IL-8 and ENA-78 mRNA levels in a dose dependent manner. Budesonide 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 16220077-7 2005 The inhibitors of ERK 1/2 (PD98059), p38 (SB203580) MAPK, and NF-kappaB (PDTC and MG132) significantly decreased C-reactive protein-induced IL-8 secretion in human monocytes. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 82-87 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 16220077-9 2005 Thus, our data indicate that C-reactive protein at pathologic levels increases IL-8 secretion and mRNA via enhancing ROS derived mainly from NAD(P)H oxidase and the subsequent activation of ERK1/2, p38 MAPK, and NF-kappaB. Reactive Oxygen Species 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 15950427-2 2005 Particulate wear debris induced NF-kappaB activation, the major transcriptional regulator of IL-8 and MCP-1 pro-inflammatory genes and, indeed, both IL-8 and MCP-1 chemokine gene expressions were upregulated in titanium particulate-stimulated human osteoblasts. Titanium 211-219 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 15950427-2 2005 Particulate wear debris induced NF-kappaB activation, the major transcriptional regulator of IL-8 and MCP-1 pro-inflammatory genes and, indeed, both IL-8 and MCP-1 chemokine gene expressions were upregulated in titanium particulate-stimulated human osteoblasts. Titanium 211-219 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 15950427-4 2005 Transfection of a dominant negative mutant IkappaBalpha protein that cannot be serine phosphorylated led to suppression of IL-8 promoter activity. Serine 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 16308137-8 2005 Among the groups with preeclamptic plasma stimulation, intracellular CAM-1 expression on ECs and CD11b and IL-8 receptor expressions on PMNs were lower with 500 and 1000 microM than with 300 microM of GLN. Glutamine 201-204 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 16308137-9 2005 IL-8 production from ECs and PMNs was also lower with 500 and 1000 microM than with 300 microM of GLN. Glutamine 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16308137-14 2005 GLN administration at levels similar to or higher than physiologic concentrations decreased IL-8 and CAM expressions, and PMN transmigration decreased after stimulation with preeclamptic plasma. Glutamine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 16084078-5 2005 Among the arsenic groups, the expression of CAMs on ECs and CD11b, and IL-8 receptor on PMNs was lowest with 0 microM compared with the other GLN concentrations. Glutamine 142-145 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 16084078-7 2005 IL-8 secretions from ECs and PMNs were higher with 300 muM than with 600 and 1000 microM GLN, and this was consistent with the expression of the IL-8 receptor on PMNs. Glutamine 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 16084078-7 2005 IL-8 secretions from ECs and PMNs were higher with 300 muM than with 600 and 1000 microM GLN, and this was consistent with the expression of the IL-8 receptor on PMNs. Glutamine 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 16084078-12 2005 Glutamine administration at levels similar to or higher than physiological concentrations reduced IL-8 and adhesion molecule expression; PMN transmigration was also decreased after stimulation with arsenic. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 16061772-5 2005 Furthermore, we show for the first time that cigarette smoke synergizes with proinflammatory cytokines IL-1beta and tumor necrosis factor-alpha, and it is this interaction that confers steroid resistance to smoke-induced CXCL8 release. Steroids 185-192 C-X-C motif chemokine ligand 8 Homo sapiens 221-226 15888346-0 2005 Novel p38 MAP kinase inhibitor R-130823 suppresses IL-6, IL-8 and MMP-13 production in spheroid culture of human synovial sarcoma cell line SW 982. 2-(4-fluorophenyl)-4-(1-phenethyl-1,2,3,6-tetrahydropyridin-4-yl)-3-(pyridin-4-yl)-1H-pyrrole 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 15888346-8 2005 A novel p38 MAP kinase inhibitor, R-130823, inhibited the release of IL-6, IL-8 and MMP-13 in a concentration-dependent manner, but not that of IL-1beta or MMP-2. 2-(4-fluorophenyl)-4-(1-phenethyl-1,2,3,6-tetrahydropyridin-4-yl)-3-(pyridin-4-yl)-1H-pyrrole 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 15893895-8 2005 CA also inhibited interleukin-8 and tumor necrosis factor-alpha secretion from the phorbol 12-myristate 13-acetate and A23187-induced HMC-1 cells (human mast cell line). Tetradecanoylphorbol Acetate 83-114 C-X-C motif chemokine ligand 8 Homo sapiens 18-63 16210650-3 2005 We now report that LPA potently induces the generation of proinflammatory chemokines (MIP-1beta, IL-8, and MCP-1) by hMCs by a mechanism that absolutely requires IL-4. lysophosphatidic acid 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 16273626-12 2005 The concentrations of IL-6 and IL-8 in ciglitazone group were lower than those in inflammatory control group (P<0.05). ciglitazone 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 15893895-8 2005 CA also inhibited interleukin-8 and tumor necrosis factor-alpha secretion from the phorbol 12-myristate 13-acetate and A23187-induced HMC-1 cells (human mast cell line). Calcimycin 119-125 C-X-C motif chemokine ligand 8 Homo sapiens 18-63 15976375-2 2005 Binding of IL-8 to heparan sulfate (HS)-containing proteoglycans (HSPG) facilitates binding of the chemokine to its specific receptor, stabilizes and prolongs IL-8 activity, and protects it from proteolysis. Heparitin Sulfate 19-34 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 16185062-1 2005 We have used trimethylamine N-oxide (TMAO), a protecting osmolyte, to dissect the complex thermodynamic linkages involved in the interaction between the chemokine interleukin-8 (IL-8) and the N-domain of its receptor CXCR1. trimethyloxamine 13-35 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 16185062-1 2005 We have used trimethylamine N-oxide (TMAO), a protecting osmolyte, to dissect the complex thermodynamic linkages involved in the interaction between the chemokine interleukin-8 (IL-8) and the N-domain of its receptor CXCR1. trimethyloxamine 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 15976375-2 2005 Binding of IL-8 to heparan sulfate (HS)-containing proteoglycans (HSPG) facilitates binding of the chemokine to its specific receptor, stabilizes and prolongs IL-8 activity, and protects it from proteolysis. Heparitin Sulfate 19-34 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 15976375-2 2005 Binding of IL-8 to heparan sulfate (HS)-containing proteoglycans (HSPG) facilitates binding of the chemokine to its specific receptor, stabilizes and prolongs IL-8 activity, and protects it from proteolysis. Heparitin Sulfate 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 15976375-2 2005 Binding of IL-8 to heparan sulfate (HS)-containing proteoglycans (HSPG) facilitates binding of the chemokine to its specific receptor, stabilizes and prolongs IL-8 activity, and protects it from proteolysis. Heparitin Sulfate 36-38 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 16413516-4 2005 Adenosine pretreatment resulted in a reduction in IL-8 expression and secretion in response to TNF-alpha, IL-1, LPS, and PMA. Adenosine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 16279568-11 2005 Compared with placebo use, montelukast treatment decreased serum and sputum levels of eosinophil cationic protein and IL-8, decreased sputum levels of myeloperoxidase, and increased serum and sputum levels of IL-10 (P < .001 for all). montelukast 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 16236838-7 2005 RESULTS: Formoterol therapy significantly reduced sputum IL-8 levels and neutrophil numbers compared to placebo. Formoterol Fumarate 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 16236838-8 2005 There was a significant correlation between the reduction in sputum IL-8 levels and the number of neutrophils, indicating that formoterol may attenuate neutrophilic airway inflammation by inhibiting IL-8 production. Formoterol Fumarate 127-137 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 16000389-7 2005 Freshly isolated monocytes responded to the PAR-2 AP ASKH 95 (2-furoyl-LIGKV-OH) with the generation of a calcium flux and production of interleukin (IL)-1beta, IL-6, and IL-8. 2-furoyl-leucyl-isoleucyl-glycyl-lysyl-valine 62-79 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 16236838-8 2005 There was a significant correlation between the reduction in sputum IL-8 levels and the number of neutrophils, indicating that formoterol may attenuate neutrophilic airway inflammation by inhibiting IL-8 production. Formoterol Fumarate 127-137 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 16236942-7 2005 RESULTS: Dexamethasone modulated the SIRS with lower proinflammatory (IL-6, IL-8) and higher antiinflammatory (IL-10) IL levels. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 16285544-3 2005 NaF of four different concentrations (1.23%, 2%, 3% and 0%) was added into 35% phosphoric acid. phosphoric acid 79-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 16183791-2 2005 Since fluoride is known as an inhibitor of glycolytic enzymes, we investigated the possible connection between NaF-induced apoptosis and glycolysis in human promyelocytic leukemia HL-60 cells. Fluorides 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 16183791-5 2005 Utilization of glucose was nearly halted by NaF, whereas that of glutamine was rather enhanced. Glucose 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 16215365-10 2005 Interleukin-8 increased significantly in the bronchoalveolar lavage fluid (BALF) in supine-HFOV and prone-HFOV groups compared with prone-CV and supine-CV. hfov 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 16215365-10 2005 Interleukin-8 increased significantly in the bronchoalveolar lavage fluid (BALF) in supine-HFOV and prone-HFOV groups compared with prone-CV and supine-CV. hfov 106-110 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 16308450-4 2005 We have found, that pentazocine, SKF 10 047, dextrorphan reduce spontaneous secretion of IL-8, IL-6 and IL-10 and selectively changes synthesis of IL-4 by Jurkat human T lymphocyte cells lines. Pentazocine 20-31 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 16308450-4 2005 We have found, that pentazocine, SKF 10 047, dextrorphan reduce spontaneous secretion of IL-8, IL-6 and IL-10 and selectively changes synthesis of IL-4 by Jurkat human T lymphocyte cells lines. 1,2,3,4-tetrahydroisoquinoline-7-sulfonamide 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 16308450-4 2005 We have found, that pentazocine, SKF 10 047, dextrorphan reduce spontaneous secretion of IL-8, IL-6 and IL-10 and selectively changes synthesis of IL-4 by Jurkat human T lymphocyte cells lines. Dextrorphan 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 16308450-6 2005 Spontaneous secretion of IL-4 and IL-8 correlates with synthesis of nitric oxide, suggesting that NO and transitory S-nitrosylation of up-stream proteins participate in the sigma ligand dependent expression of IL-4 and IL-8 genes. Nitric Oxide 68-80 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 16308450-6 2005 Spontaneous secretion of IL-4 and IL-8 correlates with synthesis of nitric oxide, suggesting that NO and transitory S-nitrosylation of up-stream proteins participate in the sigma ligand dependent expression of IL-4 and IL-8 genes. Nitric Oxide 68-80 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 16150115-11 2005 Interleukin-8 and tumor necrosis factor-alpha levels tended to be lower in individuals who had taken melatonin following hard physical activity and a larger sample size may show significance. Melatonin 101-110 C-X-C motif chemokine ligand 8 Homo sapiens 0-45 16150112-1 2005 We evaluated the presence of the melatonin metabolite N1-acetyl-N2-formyl-5-methoxykynuramine (AFMK), in cerebrospinal fluid (CSF) of patients with viral meningitis (n = 20) and control samples (n = 8) and correlate AFMK levels with inflammatory markers such as cellularity, protein, tumor necrosis factor (TNF)-alpha, interleukin (IL)-8 and IL-1beta levels. Melatonin 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 319-337 16123332-2 2005 Peroxynitrite (ONOO-) may function as an intracellular signal for the production of IL-8; however, it is not known whether CRP regulates these events. Peroxynitrous Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 16192891-11 2005 Exogenous H2O2 enhanced IL-8 secretion and N-acetyl cysteine (NAC) prevented IL-1alpha-induced ROS production and IL-8 secretion. Acetylcysteine 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 16192891-15 2005 CONCLUSIONS: These results suggest that MAPK/AP-1 and ROS/NF-kappaB signaling pathways are involved in IL-1alpha-induced IL-8 secretion and that these paracrine signaling pathways enhance endothelial cell proliferation. Reactive Oxygen Species 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 16123332-0 2005 Loss of pentameric symmetry in C-reactive protein induces interleukin-8 secretion through peroxynitrite signaling in human neutrophils. Peroxynitrous Acid 90-103 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 16192891-0 2005 Interleukin-1alpha enhances IL-8 secretion through p38 mitogen-activated protein kinase and reactive oxygen species signaling in human pancreatic cancer cells. Reactive Oxygen Species 92-115 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 16192891-11 2005 Exogenous H2O2 enhanced IL-8 secretion and N-acetyl cysteine (NAC) prevented IL-1alpha-induced ROS production and IL-8 secretion. Hydrogen Peroxide 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 16192891-11 2005 Exogenous H2O2 enhanced IL-8 secretion and N-acetyl cysteine (NAC) prevented IL-1alpha-induced ROS production and IL-8 secretion. Acetylcysteine 43-60 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 16157236-6 2005 In addition, DL-homocysteine at the pathophysiologic dose of 25 microg/mL (185 microM) induced mRNA and protein expressions of inflammatory cytokines tumor necrosis factor-alpha, IL-1beta, interleukin-6, interleukin-8, and interleukin-12. DL-Homocysteine 13-28 C-X-C motif chemokine ligand 8 Homo sapiens 204-217 16140223-10 2005 Inhaled steroids resulted in reduced levels of IL-1 beta, IL-6, IL-8, IL-10, and IL-12 (all: P<0.01) in stable COPD (all: ex-smokers) with dose dependency for IL-8, IL-1 beta and IL-12. Steroids 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 16140223-10 2005 Inhaled steroids resulted in reduced levels of IL-1 beta, IL-6, IL-8, IL-10, and IL-12 (all: P<0.01) in stable COPD (all: ex-smokers) with dose dependency for IL-8, IL-1 beta and IL-12. Steroids 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 16123332-2 2005 Peroxynitrite (ONOO-) may function as an intracellular signal for the production of IL-8; however, it is not known whether CRP regulates these events. oxido nitrite 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 16309584-0 2005 Heme oxygenase-1-dependent and -independent regulation of angiogenic genes expression: effect of cobalt protoporphyrin and cobalt chloride on VEGF and IL-8 synthesis in human microvascular endothelial cells. cobaltiprotoporphyrin 97-118 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 16123332-4 2005 We studied the impact of human native CRP and bioengineered mCRP that cannot rearrange into the pentameric structure on ONOO- formation and ONOO--mediated IL-8 gene expression in human leukocytes. onoo 140-144 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 16309584-0 2005 Heme oxygenase-1-dependent and -independent regulation of angiogenic genes expression: effect of cobalt protoporphyrin and cobalt chloride on VEGF and IL-8 synthesis in human microvascular endothelial cells. cobaltous chloride 123-138 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 16123332-5 2005 Incubation of human whole blood or isolated neutrophils with mCRP (0.1 to 100 microg/mL) for 4 hours increased IL-8 gene expression and secretion that was blocked approximately 70% by the NO synthase inhibitor Nomega-nitro-L-arginine methyl ester (L-NAME). NG-Nitroarginine Methyl Ester 210-246 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 16123332-5 2005 Incubation of human whole blood or isolated neutrophils with mCRP (0.1 to 100 microg/mL) for 4 hours increased IL-8 gene expression and secretion that was blocked approximately 70% by the NO synthase inhibitor Nomega-nitro-L-arginine methyl ester (L-NAME). NG-Nitroarginine Methyl Ester 248-254 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 16309584-3 2005 Here we determined the effect of CoPPIX and CoCl2 on the expression of vascular endothelial growth factor (VEGF) and interleukin-8 (IL-8), the two major angiogenic mediators, in human microvascular endothelial cells (HMEC-1). coppix 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 16408727-5 2005 RESULTS: IL-5, IL-6 and IL-8 levels in both AR and NAR groups were significantly increased (all P < 0.01 for AR group; P < 0.05, 0.05, 0.01, respectively, for NAR group, as compared with normal group), and the levels were much higher in AR group than that in NAR group (P < 0.01, 0.05, 0.01, respectively). Argon 44-46 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 16123332-7 2005 Native CRP had no detectable effect at 4 hours, whereas it enhanced IL-8 release after a 24-hour incubation that was blocked by L-NAME. NG-Nitroarginine Methyl Ester 128-134 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 16309584-3 2005 Here we determined the effect of CoPPIX and CoCl2 on the expression of vascular endothelial growth factor (VEGF) and interleukin-8 (IL-8), the two major angiogenic mediators, in human microvascular endothelial cells (HMEC-1). coppix 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 16309584-3 2005 Here we determined the effect of CoPPIX and CoCl2 on the expression of vascular endothelial growth factor (VEGF) and interleukin-8 (IL-8), the two major angiogenic mediators, in human microvascular endothelial cells (HMEC-1). cobaltous chloride 44-49 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 16123332-9 2005 These results suggest that loss of the pentameric symmetry in CRP, resulting in formation of mCRP, leads to IL-8 release from human neutrophils via peroxynitrite-mediated activation of nuclear factor-kappaB and activator protein-1. Peroxynitrous Acid 148-161 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 16309584-3 2005 Here we determined the effect of CoPPIX and CoCl2 on the expression of vascular endothelial growth factor (VEGF) and interleukin-8 (IL-8), the two major angiogenic mediators, in human microvascular endothelial cells (HMEC-1). cobaltous chloride 44-49 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 16142980-8 2005 Besides, while the condensation of silica took place after addition of NaF, the N value increased only very little with time up to the point where a small amount of mesostructured material precipitated out. Silicon Dioxide 35-41 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 16309584-4 2005 CoPPIX induced HO-1 expression and strongly enhanced VEGF and IL-8 synthesis, through the activation of VEGF and IL-8 promoters. coppix 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 16309584-4 2005 CoPPIX induced HO-1 expression and strongly enhanced VEGF and IL-8 synthesis, through the activation of VEGF and IL-8 promoters. coppix 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 16148150-0 2005 Pyocyanin and its precursor phenazine-1-carboxylic acid increase IL-8 and intercellular adhesion molecule-1 expression in human airway epithelial cells by oxidant-dependent mechanisms. Pyocyanine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 65-107 16148150-0 2005 Pyocyanin and its precursor phenazine-1-carboxylic acid increase IL-8 and intercellular adhesion molecule-1 expression in human airway epithelial cells by oxidant-dependent mechanisms. 1-phenazinecarboxylic acid 28-55 C-X-C motif chemokine ligand 8 Homo sapiens 65-107 16148150-5 2005 Moreover, phenazines enhanced cytokine-dependent increases in IL-8 and ICAM-1. Phenazines 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 16148150-7 2005 The thiol antioxidant N-acetyl cysteine, extracellular catalase, and inducible NO synthase inhibitors inhibited ICAM-1 and IL-8 increases in response to both phenazines. Sulfhydryl Compounds 4-9 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 16148150-7 2005 The thiol antioxidant N-acetyl cysteine, extracellular catalase, and inducible NO synthase inhibitors inhibited ICAM-1 and IL-8 increases in response to both phenazines. Acetylcysteine 22-39 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 16148150-7 2005 The thiol antioxidant N-acetyl cysteine, extracellular catalase, and inducible NO synthase inhibitors inhibited ICAM-1 and IL-8 increases in response to both phenazines. Phenazines 158-168 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 16148150-10 2005 These studies suggest that P. aeruginosa phenazines coordinately up-regulate chemokines (IL-8) and adhesion molecules (ICAM-1) by mechanisms that are, at least in part, oxidant dependent. Phenazines 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 16092118-6 2005 NF-kappaB was constitutively active in all human pancreatic carcinoma cell lines evaluated and liposomal curcumin consistently suppressed NF-kappaB binding (electrophoretic mobility gel shift assay) and decreased the expression of NF-kappaB-regulated gene products, including cyclooxygenase-2 (immunoblots) and interleukin-8 (enzyme-linked immunoassay), both of which have been implicated in tumor growth/invasiveness. Curcumin 105-113 C-X-C motif chemokine ligand 8 Homo sapiens 311-324 16410222-5 2005 Importantly, atorvastatin at the micromolar concentrations diminished the production of interleukin (IL)-8, a proinflammatory and proangiogenic chemokine, and inhibited the synthesis of urokinase plasminogen activator (uPA), a potent proinflammatory mediator. Atorvastatin 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 88-106 16141522-6 2005 We found that leflunomide or T0 could significantly inhibit the mRNA overexpression of interleukin-8 and intercellular adhesion molecule-1 in keratinocytes induced by anthralin. Leflunomide 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 87-138 16141522-6 2005 We found that leflunomide or T0 could significantly inhibit the mRNA overexpression of interleukin-8 and intercellular adhesion molecule-1 in keratinocytes induced by anthralin. t0 29-31 C-X-C motif chemokine ligand 8 Homo sapiens 87-138 16141522-6 2005 We found that leflunomide or T0 could significantly inhibit the mRNA overexpression of interleukin-8 and intercellular adhesion molecule-1 in keratinocytes induced by anthralin. Anthralin 167-176 C-X-C motif chemokine ligand 8 Homo sapiens 87-138 16266860-9 2005 The neonates assigned to HFOV benefited from early and sustained improvement in gas exchange, with earlier extubation and lower incidence of CLD, as compared to the neonates assigned to sIMV treatment, and showed a significant reduction of serum IL-6, IL-8 and IL-10 over time only when the HFOV treatment was administered. hfov 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 15828019-0 2005 Polyamine depletion inhibits NF-kappaB binding to DNA and interleukin-8 production in human chondrocytes stimulated by tumor necrosis factor-alpha. Polyamines 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 15828019-7 2005 Moreover, DFMO also decreased IL-8 production without affecting cellular viability. Eflornithine 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 16123706-5 2005 The aim of this study was to investigate the effects of root canal sealers N2 (zinc-oxide eugenol based) and AH Plus (epoxy resin based) on the expression of IL-6 and IL-8 mRNA gene in human osteoblastic cell line U2OS cells. Nitrogen 75-77 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 16103413-3 2005 In this study, a 21-nt synthetic small interfering RNA (siRNA; specifically designed to knockdown interleukin-8 [IL-8] expression) was delivered into HeLa cells. 21-nt 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 16103413-3 2005 In this study, a 21-nt synthetic small interfering RNA (siRNA; specifically designed to knockdown interleukin-8 [IL-8] expression) was delivered into HeLa cells. 21-nt 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 16123706-9 2005 Taken together, the activation of IL-6 and IL-8 mRNA gene expression may be one of the pathogenesis of zinc oxide-eugenol based and epoxy resin based root canal sealers-induced periapical inflammation. Zinc Oxide 103-113 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 44-69 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 44-69 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 16123706-9 2005 Taken together, the activation of IL-6 and IL-8 mRNA gene expression may be one of the pathogenesis of zinc oxide-eugenol based and epoxy resin based root canal sealers-induced periapical inflammation. Eugenol 114-121 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 44-69 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15914040-8 2005 RESULTS: PE-TCs produced significantly more IL-6, IL-8, and IL-10 than those of normal-TCs when they were cultured under normoxic condition, P < .05. 9-ethyl-N-(3,4,5-trimethoxyphenyl)carbazole-3-sulfonamide 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 182-185 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 182-185 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 16103413-5 2005 After treating the HeLa cells for 20 h with phorbol myristate acetate (PMA), IL-8 mRNA levels were induced by almost 50-fold; transfection with 30 nM IL-8-specific siRNA reduced the PMA-induced IL-8 mRNA by 80%. Tetradecanoylphorbol Acetate 182-185 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 16204787-5 2005 NAC decreased sputum eosinophil cationic protein (318 +/-73 vs. 163 +/-30 ng/ml, P<0.01) and sputum IL-8 (429 +/-80 vs. 347 +/-70 ng/ml, P<0.05). Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 16088827-4 2005 Degradation of IL-8 was the result of a single specific cleavage between 59glutamine and 60arginine within the IL-8 C-terminal alpha helix. 59glutamine 73-84 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 16088827-4 2005 Degradation of IL-8 was the result of a single specific cleavage between 59glutamine and 60arginine within the IL-8 C-terminal alpha helix. 59glutamine 73-84 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 16088827-4 2005 Degradation of IL-8 was the result of a single specific cleavage between 59glutamine and 60arginine within the IL-8 C-terminal alpha helix. 60arginine 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 16088827-4 2005 Degradation of IL-8 was the result of a single specific cleavage between 59glutamine and 60arginine within the IL-8 C-terminal alpha helix. 60arginine 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 15917399-5 2005 Depletion of PKC by phorbol-12-myristate-13-acetate (10 microM) blocked SP-induced IkappaBalpha and p65 phosphorylation and IL-8 production. Tetradecanoylphorbol Acetate 20-51 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 15917399-6 2005 The PKCdelta inhibitor rottlerin at a low concentration (1 microM), but not pseudosubstrate PKC and PKCepsilon inhibitors (10 microM), significantly reduced IL-8 secretion. rottlerin 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 15917399-8 2005 Moreover, overexpression of wild-type PKCdelta increased SP-induced IL-8 promoter- and NF-kappaB-driven luciferase activities that were rottlerin-sensitive. rottlerin 136-145 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 15914040-9 2005 Both normal-TCs and PE-TCs produced more IL-6 and IL-8 when they were cultured under hypoxic conditions. 9-ethyl-N-(3,4,5-trimethoxyphenyl)carbazole-3-sulfonamide 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 15914040-9 2005 Both normal-TCs and PE-TCs produced more IL-6 and IL-8 when they were cultured under hypoxic conditions. pe 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 15914040-9 2005 Both normal-TCs and PE-TCs produced more IL-6 and IL-8 when they were cultured under hypoxic conditions. 9-ethyl-N-(3,4,5-trimethoxyphenyl)carbazole-3-sulfonamide 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 16148071-0 2005 Resuscitation of hypoxic piglets with 100% O2 increases pulmonary metalloproteinases and IL-8. Oxygen 43-45 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 16148071-12 2005 Moreover, IL-8 concentration increased significantly in piglets that were resuscitated with 100% O2 compared with 21% O2, suggesting a marked proinflammatory response in the pulmonary tissue. Oxygen 97-99 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 16148071-12 2005 Moreover, IL-8 concentration increased significantly in piglets that were resuscitated with 100% O2 compared with 21% O2, suggesting a marked proinflammatory response in the pulmonary tissue. Oxygen 118-120 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 16321206-11 2005 CONCLUSION: Mechanical stress induces the RPE cells to express MCP-1 and IL-8, and this effect was inhibited in part by pretreatment of CD, indicating that the cytoskeleton may be involved in the effect and that these two inflammatory cytokines take a part in the early stage of development of primary retinal detachment. Cytochalasin D 136-138 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 16107255-0 2005 Histidine inhibits oxidative stress- and TNF-alpha-induced interleukin-8 secretion in intestinal epithelial cells. Histidine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 16107255-1 2005 We investigated the effect of several amino acids on the secretion of such inflammatory cytokines as interleukin-8 (IL-8) induced by hydrogen peroxide or tumor necrosis factor-alpha (TNF-alpha) in intestinal epithelial-like Caco-2 and HT-29 cells. Hydrogen Peroxide 133-150 C-X-C motif chemokine ligand 8 Homo sapiens 101-114 16107255-1 2005 We investigated the effect of several amino acids on the secretion of such inflammatory cytokines as interleukin-8 (IL-8) induced by hydrogen peroxide or tumor necrosis factor-alpha (TNF-alpha) in intestinal epithelial-like Caco-2 and HT-29 cells. Hydrogen Peroxide 133-150 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 16107255-2 2005 We found that histidine, one of the conditionally essential amino acids, significantly inhibited both hydrogen peroxide- and TNF-alpha-induced IL-8 secretion and mRNA expression in Caco-2 cells and HT-29 cells. Histidine 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 16107255-2 2005 We found that histidine, one of the conditionally essential amino acids, significantly inhibited both hydrogen peroxide- and TNF-alpha-induced IL-8 secretion and mRNA expression in Caco-2 cells and HT-29 cells. Amino Acids, Essential 50-71 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 16107255-2 2005 We found that histidine, one of the conditionally essential amino acids, significantly inhibited both hydrogen peroxide- and TNF-alpha-induced IL-8 secretion and mRNA expression in Caco-2 cells and HT-29 cells. Hydrogen Peroxide 102-119 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 16107255-3 2005 These inhibitions were dose dependent and the inhibition rate of hydrogen peroxide-induced IL-8 secretion reached more than 50% at a concentration of 25mM, with over 95% inhibition at a concentration of 50mM. Hydrogen Peroxide 65-82 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 16107255-4 2005 TNF-alpha increased the transcriptional activity of the IL-8 promoter which was significantly inhibited by treating Caco-2 cells with histidine. Histidine 134-143 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 16107255-5 2005 Histidine also abolished the NF-kappaB-dependent activation of the IL-8 promoter induced by TNF-alpha. Histidine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 16107255-6 2005 These results indicate that histidine inhibited the hydrogen peroxide- and TNF-alpha-induced IL-8 secretion at the transcriptional level in intestinal epithelial cells, suggesting that histidine has the potential to attenuate intestinal inflammation. Histidine 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 16107255-6 2005 These results indicate that histidine inhibited the hydrogen peroxide- and TNF-alpha-induced IL-8 secretion at the transcriptional level in intestinal epithelial cells, suggesting that histidine has the potential to attenuate intestinal inflammation. Hydrogen Peroxide 52-69 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 16107255-6 2005 These results indicate that histidine inhibited the hydrogen peroxide- and TNF-alpha-induced IL-8 secretion at the transcriptional level in intestinal epithelial cells, suggesting that histidine has the potential to attenuate intestinal inflammation. Histidine 185-194 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 16321207-12 2005 The concentrations of IL-8 in the supernatant of the culture fluid of THEC cells increased along with the time of stimulation of LPS and Poly: C, ligands for TLR3 and 4, and reached to 297.33 pg/ml and 229.67 pg/ml respectively 8 hours after, 10 times and 7 times those of the control group (both P < 0.05). Poly C 137-144 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 15993849-3 2005 Exposure of A549 to ethanol (0.1-1%) dose-dependently inhibited (by 15-49%) the release of G-CSF and IL-8, but not of M-CSF, triggered by IL1beta or TNFalpha. Ethanol 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 16106104-10 2005 This is the first study demonstrating strong impact of VAD treatment on circulating mediators of sIL-2R and IL-8 levels parameters. vad 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 16034135-3 2005 We have previously demonstrated that heparin-binding epidermal growth factor (EGF)-like growth factor (HB-EGF) decreases proinflammatory cytokine IL-8 and NO production in cytokine-stimulated intestinal epithelial cells by interfering with the NF-kappaB signaling pathway. Heparin 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 16091628-1 2005 TIA-1 related protein binds avidly to uridine-rich elements in mRNA and pre-mRNAs of a wide range of genes, including interleukin (IL)-8 and vascular endothelial growth factor (VEGF). Uridine 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 118-136 15805230-5 2005 DMOG significantly attenuated cytokine-induced IL-8 promoter activity and protein secretion and cytokine-induced PMN migration across human microvascular endothelial cell line HMEC-1 monolayers. oxalylglycine 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 15805230-7 2005 In DMOG-pretreated (20 mg/kg) animals, plasma IL-8 levels at 3 h after onset of reperfusion were 405 +/- 40 pg/ml vs. 790 +/- 40 pg/ml in saline-treated ischemia-reperfusion animals (P < 0.001). oxalylglycine 3-7 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 15805230-7 2005 In DMOG-pretreated (20 mg/kg) animals, plasma IL-8 levels at 3 h after onset of reperfusion were 405 +/- 40 pg/ml vs. 790 +/- 40 pg/ml in saline-treated ischemia-reperfusion animals (P < 0.001). Sodium Chloride 138-144 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 15805230-9 2005 Both in vitro and in vivo DMOG-attenuated IL-8 production was associated with robust HO-1 expression. oxalylglycine 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 16048981-0 2005 Nystatin induces secretion of interleukin (IL)-1beta, IL-8, and tumor necrosis factor alpha by a toll-like receptor-dependent mechanism. Nystatin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 16048981-2 2005 Herein, we demonstrate that nystatin induces interleukin (IL)-1beta, IL-8, and tumor necrosis factor alpha secretion through its activation of toll-like receptor 1 (TLR1) and TLR2. Nystatin 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 15963954-0 2005 Amphiphilic pyridinium salts block TNF alpha/NF kappa B signaling and constitutive hypersecretion of interleukin-8 (IL-8) from cystic fibrosis lung epithelial cells. pyridinium salts 12-28 C-X-C motif chemokine ligand 8 Homo sapiens 101-114 15963954-0 2005 Amphiphilic pyridinium salts block TNF alpha/NF kappa B signaling and constitutive hypersecretion of interleukin-8 (IL-8) from cystic fibrosis lung epithelial cells. pyridinium salts 12-28 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 15963954-3 2005 In a systematic search for candidate drugs that might be used therapeutically to suppress IL-8 secretion from these cells, we have identified a potent and efficacious series of amphiphilic pyridinium salts. pyridinium salts 189-205 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 16011519-9 2005 Furthermore, BAY11-7082, an inhibitor of NF-kappaB activation, significantly reduced the IL-8 production, NF-kappaB binding activity and IkappaB-alpha degradation induced by V. vulnificus infection. 3-(4-methylphenylsulfonyl)-2-propenenitrile 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 15912140-6 2005 Release of IL-6, IL-8 and TNF-alpha was inhibited by 82-93% at 100 microM quercetin and kaempferol, and 31-70% by myricetin and morin. Quercetin 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 15912140-6 2005 Release of IL-6, IL-8 and TNF-alpha was inhibited by 82-93% at 100 microM quercetin and kaempferol, and 31-70% by myricetin and morin. kaempferol 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 15912140-6 2005 Release of IL-6, IL-8 and TNF-alpha was inhibited by 82-93% at 100 microM quercetin and kaempferol, and 31-70% by myricetin and morin. myricetin 114-123 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 15997464-9 2005 Treatment with NS-398 severely diminished the IgE-dependently induced production of IL-8 and TNF-alpha. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 15-21 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 16029496-10 2005 The effects of CSE on IL-8 release were inhibited by glutathione (GSH) and associated with the induction of the oxidant sensing protein, heme oxygenase-1. Glutathione 53-64 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 15943769-4 2005 The production of vascular endothelial growth factor (VEGF), interleukin (IL)-6 and IL-8 by HGF increased following stimulation with estradiol or progesterone, at concentrations comparable to those present in the plasma of pregnant women. Estradiol 133-142 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 15943769-4 2005 The production of vascular endothelial growth factor (VEGF), interleukin (IL)-6 and IL-8 by HGF increased following stimulation with estradiol or progesterone, at concentrations comparable to those present in the plasma of pregnant women. Progesterone 146-158 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 15961066-0 2005 Irsogladine maleate influences the response of gap junctional intercellular communication and IL-8 of human gingival epithelial cells following periodontopathogenic bacterial challenge. irsogladine 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16085794-7 2005 The augmented IL-8 mRNA expression in cord blood was inhibited by actinomycin D but enhanced by cycloheximide, suggesting that IL-8 production is controlled by de novo transcriptional induction as well as posttranscriptional up-regulation of IL-8 by neonatal leukocytes, relating to the development of CLD. Dactinomycin 66-79 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16085794-7 2005 The augmented IL-8 mRNA expression in cord blood was inhibited by actinomycin D but enhanced by cycloheximide, suggesting that IL-8 production is controlled by de novo transcriptional induction as well as posttranscriptional up-regulation of IL-8 by neonatal leukocytes, relating to the development of CLD. Cycloheximide 96-109 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 16085794-7 2005 The augmented IL-8 mRNA expression in cord blood was inhibited by actinomycin D but enhanced by cycloheximide, suggesting that IL-8 production is controlled by de novo transcriptional induction as well as posttranscriptional up-regulation of IL-8 by neonatal leukocytes, relating to the development of CLD. Cycloheximide 96-109 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 16085794-7 2005 The augmented IL-8 mRNA expression in cord blood was inhibited by actinomycin D but enhanced by cycloheximide, suggesting that IL-8 production is controlled by de novo transcriptional induction as well as posttranscriptional up-regulation of IL-8 by neonatal leukocytes, relating to the development of CLD. Cycloheximide 96-109 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 16029496-10 2005 The effects of CSE on IL-8 release were inhibited by glutathione (GSH) and associated with the induction of the oxidant sensing protein, heme oxygenase-1. Glutathione 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 16029496-11 2005 CONCLUSION: Cigarette smoke may directly cause the release of IL-8 from HASMC, an effect enhanced by TNF-alpha which is overexpressed in COPD. hasmc 72-77 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 15920037-8 2005 (4) The relevance of our findings to human disease was suggested by a TTA-mediated downregulation of serum levels of soluble VCAM-1 and IL-8 in psoriasis patients. 1-(carboxymethylthio)tetradecane 70-73 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 15728708-6 2005 LPA also induced interleukin-8 (IL-8) synthesis in the colon cancer cells by primarily activating LPA2 receptor. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 17-30 15728708-6 2005 LPA also induced interleukin-8 (IL-8) synthesis in the colon cancer cells by primarily activating LPA2 receptor. lysophosphatidic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 16098254-0 2005 Gene polymorphisms of epidermal growth factor receptor and its downstream effector, interleukin-8, predict oxaliplatin efficacy in patients with advanced colorectal cancer. Oxaliplatin 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 15958071-6 2005 The IL-8 secretion was inhibited by heat shock and butyrate concentrations as low as 0.2 m M for crypt-like and 1 m M for villous-like cells. Butyrates 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 15958071-7 2005 In a dose-dependent manner, higher butyrate concentrations enhanced IL-8 secretion to maximal levels followed by a gradual but stable decline. Butyrates 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 15958071-11 2005 We conclude that heat shock and low concentrations of butyrate inhibit IL-8 production by Caco-2 cells exposed to S. serovar Enteritidis. Butyrates 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 15972489-8 2005 Exogenous PGE2 was able to induce interleukin-8 release in HeLa 229 epithelial cells. Dinoprostone 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 15994397-6 2005 In contrast with both control groups, surfactant-depleted animals challenged with GBS and conventional ventilation showed high levels of interleukin (IL)-8, tumour necrosis factor (TNF)-alpha and myeloperoxidase in bronchoalveolar lavage fluid after 5 h of ventilation. gbs 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 137-155 16273761-0 2005 Behcet"s disease patients present high levels of deglycosylated anti-lipoteichoic acid IgG and high IL-8 production after lipoteichoic acid stimulation. lipoteichoic acid 122-139 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 15922727-3 2005 Single substitution of Cys residues present in the three extracellular loops (C119L, C196L, C286S) or in the seventh-transmembrane (TM) domain (C308L) abolished CXCL8 agonist binding, while no Cys substitution abolished surface receptor expression. Cysteine 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 161-166 15922727-7 2005 We also show that every Cys substitution in CXCR2, including those that still bind CXCL8, results in an impairment of receptor activity, analyzed as cell chemotaxis and intracellular signaling, suggesting that some structural requirement is likely fulfilled by Cys presence. Cysteine 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 15922727-7 2005 We also show that every Cys substitution in CXCR2, including those that still bind CXCL8, results in an impairment of receptor activity, analyzed as cell chemotaxis and intracellular signaling, suggesting that some structural requirement is likely fulfilled by Cys presence. Cysteine 261-264 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 15972489-9 2005 Finally, we demonstrated that interleukin-8 induction by Chlamydia infection or PGE2 treatment was dependent on extracellular signal-regulated kinase/mitogen-activated protein activity. Dinoprostone 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 16091123-2 2005 This study aimed to examine the signal pathway in the production of cytokines [interleukin-8 (IL-8) and tumour necrosis factor-alpha (TNF-alpha)] by ROS generated from phorbol myristate acetate (PMA)-stimulated human mast cell line-1 cells (HMC-1). Reactive Oxygen Species 149-152 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 15980221-6 2005 RESULTS: Both triptolide and dexamethasone inhibited in a dose-dependent manner the expression of IL-8 and MCP-1 in corneal fibroblasts induced by the proinflammatory cytokines IL-1beta or tumor necrosis factor (TNF)-alpha. triptolide 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 15980221-6 2005 RESULTS: Both triptolide and dexamethasone inhibited in a dose-dependent manner the expression of IL-8 and MCP-1 in corneal fibroblasts induced by the proinflammatory cytokines IL-1beta or tumor necrosis factor (TNF)-alpha. Dexamethasone 29-42 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 15980221-10 2005 CONCLUSIONS: Like dexamethasone, triptolide inhibited IL-8 and MCP-1 expression in cultured human corneal fibroblasts exposed to proinflammatory cytokines, an action most likely mediated by inhibition of NF-kappaB activation. triptolide 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 15927671-1 2005 We previously reported the induction of interleukin-8 (IL-8), one of the CXC chemokines, by all-trans retinoic acid (ATRA) in PL-21 and NB4 human myeloid leukemia cells, which may be implicated in APL differentiation syndrome that is a relatively frequent complication in patients with acute promyelocytic leukemia (APL) during treatment with ATRA. Tretinoin 102-115 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 15927671-1 2005 We previously reported the induction of interleukin-8 (IL-8), one of the CXC chemokines, by all-trans retinoic acid (ATRA) in PL-21 and NB4 human myeloid leukemia cells, which may be implicated in APL differentiation syndrome that is a relatively frequent complication in patients with acute promyelocytic leukemia (APL) during treatment with ATRA. Tretinoin 102-115 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 15927671-1 2005 We previously reported the induction of interleukin-8 (IL-8), one of the CXC chemokines, by all-trans retinoic acid (ATRA) in PL-21 and NB4 human myeloid leukemia cells, which may be implicated in APL differentiation syndrome that is a relatively frequent complication in patients with acute promyelocytic leukemia (APL) during treatment with ATRA. Tretinoin 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 15927671-1 2005 We previously reported the induction of interleukin-8 (IL-8), one of the CXC chemokines, by all-trans retinoic acid (ATRA) in PL-21 and NB4 human myeloid leukemia cells, which may be implicated in APL differentiation syndrome that is a relatively frequent complication in patients with acute promyelocytic leukemia (APL) during treatment with ATRA. Tretinoin 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 15927671-1 2005 We previously reported the induction of interleukin-8 (IL-8), one of the CXC chemokines, by all-trans retinoic acid (ATRA) in PL-21 and NB4 human myeloid leukemia cells, which may be implicated in APL differentiation syndrome that is a relatively frequent complication in patients with acute promyelocytic leukemia (APL) during treatment with ATRA. Tretinoin 343-347 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 15927671-1 2005 We previously reported the induction of interleukin-8 (IL-8), one of the CXC chemokines, by all-trans retinoic acid (ATRA) in PL-21 and NB4 human myeloid leukemia cells, which may be implicated in APL differentiation syndrome that is a relatively frequent complication in patients with acute promyelocytic leukemia (APL) during treatment with ATRA. Tretinoin 343-347 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 15927671-5 2005 APL cells prepared from two APL patients showed gene expression of chemokines, such as IL-8, MCP-1, MIP-1alpha, and MIP-1beta when stimulated with ATRA in vitro. Tretinoin 147-151 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 15927671-6 2005 Furthermore, serum levels of IL-8, MIP-1beta and RANTES were increased during the course of ATRA treatment in both APL patients who developed APL differentiation syndrome. Tretinoin 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 16444871-9 2005 Exogenous ADMA also stimulated secretion of monocyte chemotactic protein-1 and interleukin-8. N,N-dimethylarginine 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 15955209-9 2005 Therapeutic administration of sulfasalazine effectively downregulated the activation of NF-kappaB and the expression of IL-1beta mRNA and IL-8 mRNA while IkappaBalpha levels were stable. Sulfasalazine 30-43 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 15982617-8 2005 Using SB203580, a specific inhibitor of p38 MAPK, we detected a concentration-dependent inhibition of IL-17--induced IL-8 production with a maximal decrease of 63 +/- 5% (n=8, p<0.01). SB 203580 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 15982617-9 2005 Curcumin, a specific inhibitor of JNK, also concentration-dependently reduced IL-17--induced IL-8 production, with a maximal decrease of 82+/-4% (n=8, p<0.01). Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 15982617-11 2005 Pyrrolydine dithiocarbamate (PDTC), an inhibitor of NF-kappaB, caused a 70+/-5% (n=8, p<0.01) decrease in IL-17--induced IL-8 production. pyrrolydine dithiocarbamate 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 15982617-11 2005 Pyrrolydine dithiocarbamate (PDTC), an inhibitor of NF-kappaB, caused a 70+/-5% (n=8, p<0.01) decrease in IL-17--induced IL-8 production. prolinedithiocarbamate 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 15982617-13 2005 We also found that p38MAPK, JNK, p42/p44 ERK and NF-kappaB play an important role in IL-17--induced IL-8 production in HASMC in vitro. hasmc 119-124 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 15821150-5 2005 At low concentrations (<0.1 microM), 15d-PGJ(2) inhibited IL-1beta-stimulated prostaglandin E(2) (PGE(2)) but not cytokine (IL-6/IL-8) production or cyclooxygenase-2 (COX-2) expression. 15d-pgj 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 16091123-2 2005 This study aimed to examine the signal pathway in the production of cytokines [interleukin-8 (IL-8) and tumour necrosis factor-alpha (TNF-alpha)] by ROS generated from phorbol myristate acetate (PMA)-stimulated human mast cell line-1 cells (HMC-1). Reactive Oxygen Species 149-152 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16091123-2 2005 This study aimed to examine the signal pathway in the production of cytokines [interleukin-8 (IL-8) and tumour necrosis factor-alpha (TNF-alpha)] by ROS generated from phorbol myristate acetate (PMA)-stimulated human mast cell line-1 cells (HMC-1). Tetradecanoylphorbol Acetate 168-193 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 16091123-2 2005 This study aimed to examine the signal pathway in the production of cytokines [interleukin-8 (IL-8) and tumour necrosis factor-alpha (TNF-alpha)] by ROS generated from phorbol myristate acetate (PMA)-stimulated human mast cell line-1 cells (HMC-1). Tetradecanoylphorbol Acetate 168-193 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16091123-2 2005 This study aimed to examine the signal pathway in the production of cytokines [interleukin-8 (IL-8) and tumour necrosis factor-alpha (TNF-alpha)] by ROS generated from phorbol myristate acetate (PMA)-stimulated human mast cell line-1 cells (HMC-1). Tetradecanoylphorbol Acetate 195-198 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 16091123-2 2005 This study aimed to examine the signal pathway in the production of cytokines [interleukin-8 (IL-8) and tumour necrosis factor-alpha (TNF-alpha)] by ROS generated from phorbol myristate acetate (PMA)-stimulated human mast cell line-1 cells (HMC-1). Tetradecanoylphorbol Acetate 195-198 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 15701058-8 2005 The expression of IL-8 mRNA was increased in a dose-dependent manner after stimulation with CRP (1-100 microg/ml), whereas expression of IL-8 mRNA induced by CRP (50 microg/ml) was significantly diminished by 5 microM pitavastatin. pitavastatin 218-230 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 15746434-3 2005 We found that the IL-8 mRNA expression in lung cancer cells significantly increased after coculture with phorbol myristate acetate-treated THP-1 cells and human primary lung macrophages. Tetradecanoylphorbol Acetate 105-130 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 15746434-5 2005 The addition of anti-inflammatory agents pyrrolidine dithiocarbamate, pentoxifylline, aspirin, and dexamethasone could completely suppress the expression of IL-8 mRNA in fresh/sensitized lung cancer cell cocultures. pyrrolidine dithiocarbamic acid 41-68 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 15746434-5 2005 The addition of anti-inflammatory agents pyrrolidine dithiocarbamate, pentoxifylline, aspirin, and dexamethasone could completely suppress the expression of IL-8 mRNA in fresh/sensitized lung cancer cell cocultures. Pentoxifylline 70-84 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 15746434-5 2005 The addition of anti-inflammatory agents pyrrolidine dithiocarbamate, pentoxifylline, aspirin, and dexamethasone could completely suppress the expression of IL-8 mRNA in fresh/sensitized lung cancer cell cocultures. Aspirin 86-93 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 15746434-5 2005 The addition of anti-inflammatory agents pyrrolidine dithiocarbamate, pentoxifylline, aspirin, and dexamethasone could completely suppress the expression of IL-8 mRNA in fresh/sensitized lung cancer cell cocultures. Dexamethasone 99-112 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 15948980-8 2005 In some OLP patients with the serum IL-6 or IL-8 levels higher than the upper limit of normal serum concentration, treatment with levamisole for a period of 0.5-6.0 months could significantly reduce the mean serum IL-6 level from 14.3 +/- 1.9 pg mL(-1) to 3.2 +/- 0.6 pg mL(-1) (P < 0.001) and could significantly reduce the mean serum IL-8 level from 95.8 +/- 17.1 pg mL(-1) to 14.8 +/- 5.8 pg mL(-1) (P < 0.001). Levamisole 130-140 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 15948980-8 2005 In some OLP patients with the serum IL-6 or IL-8 levels higher than the upper limit of normal serum concentration, treatment with levamisole for a period of 0.5-6.0 months could significantly reduce the mean serum IL-6 level from 14.3 +/- 1.9 pg mL(-1) to 3.2 +/- 0.6 pg mL(-1) (P < 0.001) and could significantly reduce the mean serum IL-8 level from 95.8 +/- 17.1 pg mL(-1) to 14.8 +/- 5.8 pg mL(-1) (P < 0.001). Levamisole 130-140 C-X-C motif chemokine ligand 8 Homo sapiens 339-343 15948980-10 2005 Levamisole can modulate both the serum IL-6 and IL-8 levels in OLP patients. Levamisole 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 15948980-11 2005 IL-8, like IL-6, is also a useful serum marker in evaluating the therapeutic effects of levamisole on OLP patients. Levamisole 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15974585-3 2005 (R)-Ketoprofen (1) was previously reported to be a potent and specific noncompetitive inhibitor of CXCL8-induced human PMNs chemotaxis. Ketoprofen 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 15862344-0 2005 Interleukin-8 primes oxidative burst in neutrophil-like HL-60 through changes in cytosolic calcium. Calcium 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 15862344-3 2005 Proinflammatory cytokines such as interleukin-8 (IL-8) may modulate ROS generation through a priming phenomenon. Reactive Oxygen Species 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 15862344-3 2005 Proinflammatory cytokines such as interleukin-8 (IL-8) may modulate ROS generation through a priming phenomenon. Reactive Oxygen Species 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 15862344-4 2005 The aim of this study was to determine the effect of human IL-8 on ROS production in neutrophil-like dimethylsulfoxide-differentiated HL-60 cells (not equalHL-60 cells) and further to examine the role of Ca(2+) mobilization during the priming. Reactive Oxygen Species 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 15862344-4 2005 The aim of this study was to determine the effect of human IL-8 on ROS production in neutrophil-like dimethylsulfoxide-differentiated HL-60 cells (not equalHL-60 cells) and further to examine the role of Ca(2+) mobilization during the priming. Dimethyl Sulfoxide 101-118 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 15862344-5 2005 IL-8 at 10 nM induced no ROS production but a [Ca(2+)](i) rise (254 +/- 36 nM). Reactive Oxygen Species 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15862344-6 2005 IL-8 induced a strongly enhanced (2 fold) ROS release during stimulation with 1 microM of N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLF). Reactive Oxygen Species 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15862344-6 2005 IL-8 induced a strongly enhanced (2 fold) ROS release during stimulation with 1 microM of N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLF). N-Formylmethionine Leucyl-Phenylalanine 90-135 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15862344-6 2005 IL-8 induced a strongly enhanced (2 fold) ROS release during stimulation with 1 microM of N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLF). N-Formylmethionine Leucyl-Phenylalanine 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15893694-6 2005 Furthermore, IL-17 induction of CXCL-8 mRNA and protein release from ASM cells was abrogated by transcriptional inhibitor actinomycin D. Dactinomycin 122-135 C-X-C motif chemokine ligand 8 Homo sapiens 32-38 15701058-0 2005 Inhibitory effect of pitavastatin (NK-104) on the C-reactive-protein-induced interleukin-8 production in human aortic endothelial cells. pitavastatin 21-33 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 15701058-0 2005 Inhibitory effect of pitavastatin (NK-104) on the C-reactive-protein-induced interleukin-8 production in human aortic endothelial cells. pitavastatin 35-41 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 15701058-3 2005 In the present study, we examined the effect of pitavastatin (NK-104), a synthetic statin (3-hydroxy-3-methylglutaryl CoA reductase inhibitor), on IL-8 production induced by CRP in human AoEC (aortic endothelial cells). pitavastatin 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 15701058-3 2005 In the present study, we examined the effect of pitavastatin (NK-104), a synthetic statin (3-hydroxy-3-methylglutaryl CoA reductase inhibitor), on IL-8 production induced by CRP in human AoEC (aortic endothelial cells). pitavastatin 62-68 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 15701058-7 2005 The production of IL-8 induced by CRP (10 microg/ml) was enhanced significantly and was inhibited by pitavastatin. pitavastatin 101-113 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 15701058-8 2005 The expression of IL-8 mRNA was increased in a dose-dependent manner after stimulation with CRP (1-100 microg/ml), whereas expression of IL-8 mRNA induced by CRP (50 microg/ml) was significantly diminished by 5 microM pitavastatin. pitavastatin 218-230 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 15701058-9 2005 Furthermore, specific MAPK inhibitors (PD98059, SB203580 and SP600125) inhibited the expression of IL-8 mRNA induced by CRP (50 microg/ml). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 15701058-9 2005 Furthermore, specific MAPK inhibitors (PD98059, SB203580 and SP600125) inhibited the expression of IL-8 mRNA induced by CRP (50 microg/ml). SB 203580 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 15701058-9 2005 Furthermore, specific MAPK inhibitors (PD98059, SB203580 and SP600125) inhibited the expression of IL-8 mRNA induced by CRP (50 microg/ml). pyrazolanthrone 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 15701058-11 2005 Our results suggest that CRP may play a role in atherosclerosis via IL-8 production and pitavastatin may prevent the progression of atherosclerosis not only by lowering plasma low-density lipoprotein cholesterol levels, but also by suppressing IL-8 production in endothelial cells through the inhibition of MAPK (ERK, p38 MAPK and JNK) pathways. pitavastatin 88-100 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 15799714-4 2005 Kibayashi and co-workers in this issue of Clinical Science confirm that CRP induces IL-8 production in human aortic endothelial cells in vitro, via the activation of MAPKs (mitogen-activated protein kinases), an effect that can be inhibited by pitavastatin. pitavastatin 244-256 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 15870903-0 2005 Inhibition of interleukin-8 production in the human colonic epithelial cell line HT-29 by 18 beta-glycyrrhetinic acid. beta-glycyrrhetinic acid 93-117 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 15924880-5 2005 Sabaeksan (1 mg/ml) inhibited PMA plus A23187-induced TNF-alpha, IL-6, and IL-8 secretion by 43.86+/-5.26%, 56.39+/-3.65%, and 63.48+/-2.54%, respectively. Calcimycin 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 15924880-5 2005 Sabaeksan (1 mg/ml) inhibited PMA plus A23187-induced TNF-alpha, IL-6, and IL-8 secretion by 43.86+/-5.26%, 56.39+/-3.65%, and 63.48+/-2.54%, respectively. sabaeksan 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 15870903-3 2005 We investigated the role of 18 beta-glycyrrhetinic acid (GA), a saponin isolated from licorice roots, on TNF-alpha-induced IL-8 production in human colonic epithelial cells. beta-glycyrrhetinic acid 31-55 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 15870903-3 2005 We investigated the role of 18 beta-glycyrrhetinic acid (GA), a saponin isolated from licorice roots, on TNF-alpha-induced IL-8 production in human colonic epithelial cells. Gallium 57-59 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 15870903-6 2005 GA suppressed TNF-alpha-induced IL-8 production in a concentration-dependent manner. Gallium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 15870903-8 2005 These results suggest that GA has the inhibitory effects on TNF-alpha-induced IL-8 production in the intestinal epithelial cells through blockade in the phosphorylation of MAPKs, following I kappa B alpha degradation and NF-kappa B activation. Gallium 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. phenylalanylleucine 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. phenylalanylleucine 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. Serine 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. Serine 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 15755849-2 2005 The expression of the prostaglandin synthetic enzyme cyclooxygenase (COX)-2 and cytokines IL-1beta and IL-8 increases within the uterus at the time of labor, and each is regulated by the transcription factor nuclear factor-kappaB (NF-kappaB). Prostaglandins 22-35 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. Leucine 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. Leucine 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. Arginine 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. Aspartic Acid 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 15755869-4 2005 Thrombin and SFLLRN (Ser-Phe-Leu-Leu-Arg-Asp), a PAR1 agonist peptide, increased the mRNA expression of IL-8, monocyte chemoattractant protein-1 (MCP-1), and cyclooxygenase-2 (COX-2) and the protein secretion of IL-8 nd MCP-1 in ESCs. Aspartic Acid 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 15755869-5 2005 The addition of thrombin inhibitor d-phenylalanyl-l-prolyl-l arginine chloromethyl ketone (PPACK) together with thrombin inhibited the thrombin-induced secretion of IL-8 and MCP-1. d-phenylalanyl-l-prolyl-l arginine chloromethyl ketone 35-89 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 15955105-10 2005 Topical application of calcipotriol to lesional psoriatic skin for 4 d resulted in increased NF-kappaB binding to the p53 kappaB site and decreased NF-kappaB binding to the IL-8 kappaB site. calcipotriene 23-35 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 15956258-4 2005 Parthenolide was effective either alone or in combination with docetaxel in reducing colony formation, inducing apoptosis and reducing the expression of prometastatic genes IL-8 and the antiapoptotic gene GADD45beta1 in vitro. Docetaxel 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 15956258-4 2005 Parthenolide was effective either alone or in combination with docetaxel in reducing colony formation, inducing apoptosis and reducing the expression of prometastatic genes IL-8 and the antiapoptotic gene GADD45beta1 in vitro. parthenolide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 16032878-1 2005 We report an experimental study of the variation of surface stress with surface charge density for nanoporous Pt immersed in aqueous solutions of NaF of various concentration. Platinum 110-112 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 15845391-4 2005 Stimulation with polyI:C elicited the elevated production and mRNA expression of IL-6 and IL-8 in HCEC. Poly I-C 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 15855050-6 2005 The early loss of ascorbate correlated with duration of CPB (P < 0.002, r = 0.72), plasma hemoglobin after cross-clamp removal (P < 0.001, r = 0.70), and IL-6 and IL-8 levels at 24 and 48 h after CPB (P < 0.01), but not with postoperative lactate levels, strongly suggesting that hemolysis, and not inflammation or ischemia, was the main cause of early oxidative stress. Ascorbic Acid 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 15879132-3 2005 Accordingly, we observed that synthetic dsRNA, polyinosinic acid:cytidylic acid (poly(I:C)), potently induced gene remodeling in model intestinal epithelia with the specific pattern of expressed genes, including both classic proinflammatory genes (e.g., IL-8), as well as genes that are classically activated in virus-infected cells (e.g., IFN-responsive genes). Poly I 47-64 C-X-C motif chemokine ligand 8 Homo sapiens 254-258 15879132-3 2005 Accordingly, we observed that synthetic dsRNA, polyinosinic acid:cytidylic acid (poly(I:C)), potently induced gene remodeling in model intestinal epithelia with the specific pattern of expressed genes, including both classic proinflammatory genes (e.g., IL-8), as well as genes that are classically activated in virus-infected cells (e.g., IFN-responsive genes). Cytidine Monophosphate 65-79 C-X-C motif chemokine ligand 8 Homo sapiens 254-258 15879132-3 2005 Accordingly, we observed that synthetic dsRNA, polyinosinic acid:cytidylic acid (poly(I:C)), potently induced gene remodeling in model intestinal epithelia with the specific pattern of expressed genes, including both classic proinflammatory genes (e.g., IL-8), as well as genes that are classically activated in virus-infected cells (e.g., IFN-responsive genes). poly 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 254-258 15879132-4 2005 Poly(I:C)-induced IL-8 was concentration dependent (2-100 mug/ml) and displayed slower kinetics compared with IL-8 induced by bacterial flagellin (ET(50) approximately 24 vs 8 h poly(I:C) vs flagellin, respectively). Poly I-C 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 16032847-1 2005 DMPC vesicles were injected into a 50 mM NaF solution in water, and the kinetics of a monolayer formation at the air-solution interface was investigated by measuring changes of the film pressure, pi, as a function of time. Dimyristoylphosphatidylcholine 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 16045029-2 2005 METHODS: Immunohistochemical method of avidin-biotin complex was used for microvessel counts on the routinely formalin-fixed and paraffin-embedded sections of specimens of hypertrophic scars, keloids, normal skin, and surgical scar, and in situ hybridization for the expressions of IL-8, MCP-1, MIP-1alpha mRNA. avidin-biotin 39-52 C-X-C motif chemokine ligand 8 Homo sapiens 282-286 15746099-8 2005 The BK-triggered increased IL-8 secretion in SMM-treated cultures was mediated by an increased Ca(2+)(i) mobilization consequent to an ER expansion associated with increases in protein synthesis (total, cytokines, and antimicrobial factors). smm 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15796906-2 2005 Recently, the hP2Y6 receptor has been reported to mediate monocyte IL-8 production in response to UDP or lipopolysaccharide (LPS), but the role of hP2Y6 in regulating other pro-inflammatory cytokines or mediators is largely unknown. Uridine Diphosphate 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 15796906-3 2005 We demonstrate here that UDP specifically induces soluble TNF-alpha and IL-8 production in a promonocytic U937 cell line stably transfected with hP2Y6. Uridine Diphosphate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 15796906-6 2005 Interestingly, UDP induces the production of IL-8, but not TNF-alpha, in human astrocytoma 1321N1 cell lines stably transfected with hP2Y6. Uridine Diphosphate 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 15796906-9 2005 From the Taqman analysis, UDP stimulation significantly upregulates the mRNA levels of IL-8, IP-10, and IL-1beta, but not TNF-alpha. Uridine Diphosphate 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 15855488-6 2005 Indolicidin was analogous to LL-37 in its ability to induce the production of the chemokine interleukin-8 (IL-8) in a human bronchial cell line, 16HBE14o(-), but it was unable to induce production of IL-8 in THP-1 cells. 16hbe14o 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 15845704-7 2005 We also analyzed the effect of NAC on interleukin-8 (IL-8)-induced expression of CD11b in human whole blood. Acetylcysteine 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 15845704-7 2005 We also analyzed the effect of NAC on interleukin-8 (IL-8)-induced expression of CD11b in human whole blood. Acetylcysteine 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 15845704-8 2005 IL-8 (10 ng/mL) significantly upregulated the expression of CD11b, and the IL-8-induced upregulation was significantly attenuated by NAC (>10 mM) in a dose-dependent manner. Acetylcysteine 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15845704-8 2005 IL-8 (10 ng/mL) significantly upregulated the expression of CD11b, and the IL-8-induced upregulation was significantly attenuated by NAC (>10 mM) in a dose-dependent manner. Acetylcysteine 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 15845704-9 2005 We conclude that NAC attenuates the increased expression of CD11b in either LPS or IL-8-stimulated human whole blood. Acetylcysteine 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 15855488-6 2005 Indolicidin was analogous to LL-37 in its ability to induce the production of the chemokine interleukin-8 (IL-8) in a human bronchial cell line, 16HBE14o(-), but it was unable to induce production of IL-8 in THP-1 cells. 16hbe14o 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 15807851-1 2005 This study was designed to investigate the relationship between influx of extracellular Ca(2+), activation of NFkappaB and synthesis of interleukin-8 (IL-8) following exposure of human neutrophils to subcytolytic concentrations (8.37 and 41.75 ng/ml) of the pneumococcal toxin, pneumolysin, as well as the potential of the omega-3 polyunsaturated fatty acid, docosahexaenoic acid, to antagonize these events. omega-3 polyunsaturated fatty acid 323-357 C-X-C motif chemokine ligand 8 Homo sapiens 136-149 15826602-4 2005 Actinomcyin D markedly reduced the upregulation of IL-6 and IL-8 mRNA. actinomcyin d 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 16161253-1 2005 We have previously reported that sodium fluoride (NaF) showed slightly higher cytotoxicity against human oral tumor cell lines than normal human oral cells. Sodium Fluoride 33-48 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 15807851-1 2005 This study was designed to investigate the relationship between influx of extracellular Ca(2+), activation of NFkappaB and synthesis of interleukin-8 (IL-8) following exposure of human neutrophils to subcytolytic concentrations (8.37 and 41.75 ng/ml) of the pneumococcal toxin, pneumolysin, as well as the potential of the omega-3 polyunsaturated fatty acid, docosahexaenoic acid, to antagonize these events. omega-3 polyunsaturated fatty acid 323-357 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 15807851-1 2005 This study was designed to investigate the relationship between influx of extracellular Ca(2+), activation of NFkappaB and synthesis of interleukin-8 (IL-8) following exposure of human neutrophils to subcytolytic concentrations (8.37 and 41.75 ng/ml) of the pneumococcal toxin, pneumolysin, as well as the potential of the omega-3 polyunsaturated fatty acid, docosahexaenoic acid, to antagonize these events. Docosahexaenoic Acids 359-379 C-X-C motif chemokine ligand 8 Homo sapiens 136-149 15807851-1 2005 This study was designed to investigate the relationship between influx of extracellular Ca(2+), activation of NFkappaB and synthesis of interleukin-8 (IL-8) following exposure of human neutrophils to subcytolytic concentrations (8.37 and 41.75 ng/ml) of the pneumococcal toxin, pneumolysin, as well as the potential of the omega-3 polyunsaturated fatty acid, docosahexaenoic acid, to antagonize these events. Docosahexaenoic Acids 359-379 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 15807851-5 2005 These observations demonstrate that activation of NFkappaB and synthesis of IL-8, following exposure of neutrophils to pneumolysin are dependent on toxin-mediated influx of Ca(2+) and that these potentially harmful activities of the toxin are antagonized by docosahexaenoic acid. Docosahexaenoic Acids 258-278 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 15661856-6 2005 Transfection with either HO-1 small interfering RNA or HO-1 antisense oligodeoxynucleotide abrogated the ability of SNAP to induce HO-1 expression and IL-8 and VEGF productions. Oligodeoxyribonucleotides 70-90 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 15661856-5 2005 The NO donor S-nitroso-N-acetyl-penicillamine (SNAP) dose-dependently increased IL-8 and VEGF productions and HO-1 expression in HUVECs. S-Nitroso-N-Acetylpenicillamine 13-45 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 15863635-9 2005 Epithelial expression of interleukin-8 showed a tendency towards a significant increase after LPS compared to saline. Sodium Chloride 110-116 C-X-C motif chemokine ligand 8 Homo sapiens 25-38 15661856-5 2005 The NO donor S-nitroso-N-acetyl-penicillamine (SNAP) dose-dependently increased IL-8 and VEGF productions and HO-1 expression in HUVECs. S-Nitroso-N-Acetylpenicillamine 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 15827963-3 2005 We here demonstrate statistically significant synergy between regakine-1 and the neutrophil attractants C5a or IL-8/CXCL8 in inducing neutrophil shape change and migration under agarose. Sepharose 178-185 C-X-C motif chemokine ligand 8 Homo sapiens 116-121 15829704-10 2005 Finally, pretreatment with AG-1478, the MEK inhibitor UO126, and NAC prevented the albumin-induced increase in IL-8 expression. RTKI cpd 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 15845465-4 2005 Maximal production of IL-8 in response to Act required the presence of intracellular calcium, since chelation of calcium with BAPTA-AM significantly reduced Act-induced IL-8 production in HT-29 cells. Calcium 85-92 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 15845465-4 2005 Maximal production of IL-8 in response to Act required the presence of intracellular calcium, since chelation of calcium with BAPTA-AM significantly reduced Act-induced IL-8 production in HT-29 cells. Calcium 85-92 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 15845465-4 2005 Maximal production of IL-8 in response to Act required the presence of intracellular calcium, since chelation of calcium with BAPTA-AM significantly reduced Act-induced IL-8 production in HT-29 cells. Calcium 113-120 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 15845465-4 2005 Maximal production of IL-8 in response to Act required the presence of intracellular calcium, since chelation of calcium with BAPTA-AM significantly reduced Act-induced IL-8 production in HT-29 cells. Calcium 113-120 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 15845465-4 2005 Maximal production of IL-8 in response to Act required the presence of intracellular calcium, since chelation of calcium with BAPTA-AM significantly reduced Act-induced IL-8 production in HT-29 cells. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 126-134 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 15845465-4 2005 Maximal production of IL-8 in response to Act required the presence of intracellular calcium, since chelation of calcium with BAPTA-AM significantly reduced Act-induced IL-8 production in HT-29 cells. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 126-134 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 15866594-1 2005 OBJECTIVE: To investigate whether and how P, dienogest (synthetic progestin), and danazol affected tumor necrosis factor alpha (TNFalpha)-induced interleukin-8 (IL-8) expression in endometriotic stromal cells. Danazol 82-89 C-X-C motif chemokine ligand 8 Homo sapiens 146-159 15866594-1 2005 OBJECTIVE: To investigate whether and how P, dienogest (synthetic progestin), and danazol affected tumor necrosis factor alpha (TNFalpha)-induced interleukin-8 (IL-8) expression in endometriotic stromal cells. Danazol 82-89 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 15866594-10 2005 The up-regulation of the IL-8 gene and protein expression by TNFalpha and E2 was significantly reduced by the addition of P, dienogest, or danazol. Danazol 139-146 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 15829704-10 2005 Finally, pretreatment with AG-1478, the MEK inhibitor UO126, and NAC prevented the albumin-induced increase in IL-8 expression. U 0126 54-59 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 15687330-0 2005 Thalidomide inhibits tumor necrosis factor-alpha-induced interleukin-8 expression in endometriotic stromal cells, possibly through suppression of nuclear factor-kappaB activation. Thalidomide 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 15829704-10 2005 Finally, pretreatment with AG-1478, the MEK inhibitor UO126, and NAC prevented the albumin-induced increase in IL-8 expression. Acetylcysteine 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 15779068-6 2005 Genistein, piceatannol, and TAS diminished secretion of TNF-alpha, and IL-8. Genistein 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 15701708-7 2005 In addition, AGIX-4207 inhibited cytokine-induced levels of monocyte chemoattractant protein-1, interleukin (IL)-6, and IL-8 from endothelial cells and human fibroblast-like synoviocytes as well as lipopolysaccharide-induced release of TNF-alpha, IL-1beta, and IL-6 from human peripheral blood mononuclear cells. camobucol 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 15829265-0 2005 Requirement of the extracellular cysteine at position six for CD40/CD40 dimer formation and CD40-induced IL-8 expression. Cysteine 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 15829265-7 2005 Abolishment of disulfide-linked CD40/CD40 dimers in these transfected cells was sufficient to inhibit CD40-induced mRNA expression and secretion of IL-8. Disulfides 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 15840782-6 2005 Exposure to NaF for 30 or 120 sec increased plaque fluoride concentrations near the saliva interface, while concentrations near the enamel surface remained low. Fluorides 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 15840782-7 2005 Fluoride penetration increased with duration of NaF exposure. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 15840783-4 2005 The phenol-water extracts activated human gingival fibroblasts to mediate IL-8 production, as well as IL-8 mRNA expression, phosphorylation of p38 mitogen-activated protein kinase, and expression of intercellular adhesion molecule-1. Phenol 4-10 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15840783-4 2005 The phenol-water extracts activated human gingival fibroblasts to mediate IL-8 production, as well as IL-8 mRNA expression, phosphorylation of p38 mitogen-activated protein kinase, and expression of intercellular adhesion molecule-1. Phenol 4-10 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 15840783-4 2005 The phenol-water extracts activated human gingival fibroblasts to mediate IL-8 production, as well as IL-8 mRNA expression, phosphorylation of p38 mitogen-activated protein kinase, and expression of intercellular adhesion molecule-1. Water 11-16 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15840783-4 2005 The phenol-water extracts activated human gingival fibroblasts to mediate IL-8 production, as well as IL-8 mRNA expression, phosphorylation of p38 mitogen-activated protein kinase, and expression of intercellular adhesion molecule-1. Water 11-16 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 15867792-11 2005 Bile acids correlated with BALF IL-8 and alveolar neutrophilia (r = 0.3, P = .0004, and r = 0.3, P = .004, respectively), but not with IL-15. Bile Acids and Salts 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 15867792-14 2005 Elevated BALF bile acids may promote early BOS development via an inflammatory process, possibly mediated by IL-8 and alveolar neutrophilia. Bile Acids and Salts 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 15779068-6 2005 Genistein, piceatannol, and TAS diminished secretion of TNF-alpha, and IL-8. 3,3',4,5'-tetrahydroxystilbene 11-22 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 15779068-6 2005 Genistein, piceatannol, and TAS diminished secretion of TNF-alpha, and IL-8. tas 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 15779068-7 2005 TAS reduced mRNA levels of COX-2, TNF-alpha, IL-8, IL-6, and IL-1alpha, while resveratrol impaired early expression of IL-8 and TNF-alpha. tas 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 15862158-9 2005 Rolipram inhibited the expression of IL-8 mRNA and the activation of NF-kappaB(P<0.05). Rolipram 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 15779068-7 2005 TAS reduced mRNA levels of COX-2, TNF-alpha, IL-8, IL-6, and IL-1alpha, while resveratrol impaired early expression of IL-8 and TNF-alpha. Resveratrol 78-89 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 15850408-4 2005 Pravastatin inhibited the overproduction of monocyte chemoattractant protein 1, IL6 and IL8 and the enhanced expression of intercellular adhesion molecule 1 but had no effect on platelet-endothelial cell adhesion molecule 1 expression. Pravastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 15862158-10 2005 CONCLUSION: The results indicated that IL-8 mRNA may play a pathogenic role in the development of COPD and that selective PDE type IV inhibitor Rolipram inhibit the expression of IL-8 mRNA via NF-kappaB. Rolipram 144-152 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 15877961-6 2005 CONCLUSION: Aloe polysaccharide could promote keratinocytes to secrete TGF-alpha, TGF-beta1, IL-1beta, IL-6, IL-8 and TNF, and inhibit the release of NO. aloe polysaccharide 12-31 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 15659384-0 2005 Prostaglandin E2 induces interleukin-8 gene transcription by activating C/EBP homologous protein in human T lymphocytes. Dinoprostone 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 25-38 15846428-1 2005 Probe beam deflection (PBD) and AC impedance are used to quantitatively evaluate the double layer properties of carbon aerogel electrodes in aqueous media (NaF). Carbon 112-118 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 15659384-3 2005 Several kinases, including protein kinase C, Src family tyrosine kinases, phosphatidylinositol 3-kinase, and p38 MAPK, were involved in PGE(2)-induced CHOP activation and IL-8 production. Dinoprostone 136-142 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 15659384-1 2005 The effect of prostaglandin E(2) (PGE(2)) in regulating the synthesis of the pro-inflammatory chemokine interleukin-8 (IL-8) in T lymphocytes is not yet defined, even though it may reduce or enhance IL-8 synthesis in other cell types. Dinoprostone 14-32 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 15659384-5 2005 Our data suggest that PGE(2) acts as a potent pro-inflammatory mediator by inducing IL-8 gene transcription in activated T cells through different signal transduction pathways leading to CHOP activation. Prostaglandins E 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 15659384-6 2005 These findings show the complexity with which PGE(2) regulates IL-8 synthesis by inhibiting or enhancing its production depending on the cell types and environmental conditions. Prostaglandins E 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 15701651-7 2005 Finally, muramyl dipeptide induced interleukin-8 production in MAIL8 cells. Acetylmuramyl-Alanyl-Isoglutamine 9-26 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 15659384-1 2005 The effect of prostaglandin E(2) (PGE(2)) in regulating the synthesis of the pro-inflammatory chemokine interleukin-8 (IL-8) in T lymphocytes is not yet defined, even though it may reduce or enhance IL-8 synthesis in other cell types. Dinoprostone 14-32 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 15659384-1 2005 The effect of prostaglandin E(2) (PGE(2)) in regulating the synthesis of the pro-inflammatory chemokine interleukin-8 (IL-8) in T lymphocytes is not yet defined, even though it may reduce or enhance IL-8 synthesis in other cell types. Dinoprostone 34-40 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 15659384-1 2005 The effect of prostaglandin E(2) (PGE(2)) in regulating the synthesis of the pro-inflammatory chemokine interleukin-8 (IL-8) in T lymphocytes is not yet defined, even though it may reduce or enhance IL-8 synthesis in other cell types. Dinoprostone 34-40 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 15659384-1 2005 The effect of prostaglandin E(2) (PGE(2)) in regulating the synthesis of the pro-inflammatory chemokine interleukin-8 (IL-8) in T lymphocytes is not yet defined, even though it may reduce or enhance IL-8 synthesis in other cell types. Dinoprostone 34-40 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 15659384-2 2005 Here, we demonstrate that, in human T cells, PGE(2) induced IL-8 mRNA transcription through prostaglandin E(2) receptors 1- and 4-dependent signal transduction pathways leading to the activation of the transcription factor C/EBP homologous protein (CHOP), never before implicated in IL-8 transcription. Prostaglandins E 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 15659384-2 2005 Here, we demonstrate that, in human T cells, PGE(2) induced IL-8 mRNA transcription through prostaglandin E(2) receptors 1- and 4-dependent signal transduction pathways leading to the activation of the transcription factor C/EBP homologous protein (CHOP), never before implicated in IL-8 transcription. Prostaglandins E 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 283-287 16061006-0 2005 [Effects of erythromycin on hydrogen peroxide-induced interleukin-8 synthesis and regulation of glutathione in human bronchial epithelial cells]. Erythromycin 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 16061006-0 2005 [Effects of erythromycin on hydrogen peroxide-induced interleukin-8 synthesis and regulation of glutathione in human bronchial epithelial cells]. Hydrogen Peroxide 28-45 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 16061006-1 2005 OBJECTIVE: To study the effects of erythromycin on Hydrogen peroxide (H2O2)-induced interleukin-8 synthesis and regulation of glutathione in human bronchial epithelial cells. Erythromycin 35-47 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 16061006-1 2005 OBJECTIVE: To study the effects of erythromycin on Hydrogen peroxide (H2O2)-induced interleukin-8 synthesis and regulation of glutathione in human bronchial epithelial cells. Hydrogen Peroxide 51-68 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 16061006-1 2005 OBJECTIVE: To study the effects of erythromycin on Hydrogen peroxide (H2O2)-induced interleukin-8 synthesis and regulation of glutathione in human bronchial epithelial cells. Hydrogen Peroxide 70-74 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 16061006-8 2005 CONCLUSION: Erythromycin inhibits oxidant-mediated IL-8 levels through down-regulation of NF-kB and AP-1 binding in HBE, which can further influence the synthesis of GSH and expression gamma-GCS in HBE. Erythromycin 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 15801837-1 2005 A novel class of 2-(R)-phenylpropionamides has been recently reported to inhibit in vitro and in vivo interleukin-8 (CXCL8)-induced biological activities. 2-(r)-phenylpropionamides 17-42 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 15801837-2 2005 These CXCL8 inhibitors are derivatives of phenylpropionic nonsteroidal antiinflammatory drugs (NSAIDs), high-affinity ligands for site II of human serum albumin (HSA). phenylpropionic 42-57 C-X-C motif chemokine ligand 8 Homo sapiens 6-11 16851713-1 2005 We present results from molecular dynamics simulation of aqueous solutions of alkali halide salts (NaI and NaF) at the interface with hydrophobic objects. halide salts 85-97 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 15801837-1 2005 A novel class of 2-(R)-phenylpropionamides has been recently reported to inhibit in vitro and in vivo interleukin-8 (CXCL8)-induced biological activities. 2-(r)-phenylpropionamides 17-42 C-X-C motif chemokine ligand 8 Homo sapiens 117-122 15777559-1 2005 Our previous study demonstrated that homocysteine (Hcy) mediated the expression and secretion of MCP-1 and IL-8 in human monocytes. Homocysteine 37-49 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 15591095-7 2005 Inhibition of ERK MAPK pathway using U0126 prevented CRP-induced IL-8 upregulation, and Western blot analysis revealed a rapid activation of ERK1/2 after CRP stimulation. U 0126 37-42 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 15777559-1 2005 Our previous study demonstrated that homocysteine (Hcy) mediated the expression and secretion of MCP-1 and IL-8 in human monocytes. Homocysteine 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 15777559-5 2005 After patients with HHcy underwent low-dose folic acid treatment (0.8 mg/d) for 6 months, plasma Hcy levels were decreased and the hyper-responsiveness of MCP-1 and IL-8 secreted by isolated monocytes was significantly reversed. Folic Acid 44-54 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 15777559-5 2005 After patients with HHcy underwent low-dose folic acid treatment (0.8 mg/d) for 6 months, plasma Hcy levels were decreased and the hyper-responsiveness of MCP-1 and IL-8 secreted by isolated monocytes was significantly reversed. Homocysteine 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 15762874-7 2005 NNKOAc mimicked NNK effects, whereas NDMAOAc significantly inhibited IL-8 production in BEAS-2B cells and MCP-1 in both cell types. methyl(acetoxymethyl)nitrosamine 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 15760459-0 2005 Mycobacterium bovis bacille Calmette Guerin infection of human neutrophils induces CXCL8 secretion by MyD88-dependent TLR2 and TLR4 activation. guerin 37-43 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 15825081-7 2005 RESULTS: TxB activates EGFR and ERK1/2 phosphorylation with subsequent release of IL-8 from human colonocytes. (2s,3r,4r,5r)-5-Sulfanyloxane-2,3,4-Triol 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 15825081-11 2005 Inhibition of MMP, EGFR, and ERK activation significantly decreased TxB-induced IL-8 expression. (2s,3r,4r,5r)-5-Sulfanyloxane-2,3,4-Triol 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 15825081-2 2005 In a xenograft animal model, TxB was shown to induce interleukin (IL)-8 gene expression in human colonic epithelium. (2s,3r,4r,5r)-5-Sulfanyloxane-2,3,4-Triol 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 53-71 15664665-4 2005 The stimulatory effect of BK on the IL-1beta- or TNFalpha-stimulated IL-8 production was reduced in the presence of BK B2 receptor antagonist HOE 140, whereas the B1 receptor antagonist Lys-(des-arg9, Leu8)-BK had no effect. des-arg9 191-199 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 15664665-6 2005 The protein kinase C (PKC) inhibitor bisindolylmaleimide, BIS, significantly reduced the stimulatory effect of BK on IL-1beta and TNFalpha increased IL-8 production but did not affect the production of IL-8 stimulated by cytokines alone. bisindolylmaleimide 37-56 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 15856410-6 2005 Using a nuclear factor-kappaB (NF-kappaB) luciferase reporter assay system and Western analysis, we identified that magnolol and honokiol exert their anti-inflammatory effects by inhibiting the NF-kappaB element, which exists in Cox-2, IL-8, and TNF-alpha promoters [(15 microM magnolol: 44.8% inhibition), (15 microM honokiol: 42.3% inhibition)]. magnolol 116-124 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 15856410-6 2005 Using a nuclear factor-kappaB (NF-kappaB) luciferase reporter assay system and Western analysis, we identified that magnolol and honokiol exert their anti-inflammatory effects by inhibiting the NF-kappaB element, which exists in Cox-2, IL-8, and TNF-alpha promoters [(15 microM magnolol: 44.8% inhibition), (15 microM honokiol: 42.3% inhibition)]. honokiol 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 15664665-6 2005 The protein kinase C (PKC) inhibitor bisindolylmaleimide, BIS, significantly reduced the stimulatory effect of BK on IL-1beta and TNFalpha increased IL-8 production but did not affect the production of IL-8 stimulated by cytokines alone. Bismuth 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 15664665-5 2005 Similar to BK, the calcium ionophore A23187 also upregulated the stimulatory effect of IL-1beta and TNFalpha on IL-8 production. Calcium 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 15664665-6 2005 The protein kinase C (PKC) inhibitor bisindolylmaleimide, BIS, significantly reduced the stimulatory effect of BK on IL-1beta and TNFalpha increased IL-8 production but did not affect the production of IL-8 stimulated by cytokines alone. Bismuth 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 15664665-7 2005 The specific p38 mitogen-activated protein kinase (MAPK) inhibitor SB 203580 reduced IL-8 production stimulated by the combination of BK and IL-1beta as well as the IL-1beta-stimulated IL-8 production. SB 203580 67-76 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 15664665-5 2005 Similar to BK, the calcium ionophore A23187 also upregulated the stimulatory effect of IL-1beta and TNFalpha on IL-8 production. Calcimycin 37-43 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 15749028-4 2005 IL-8 increased DNA synthesis of Caco2 in a dose dependent manner and this was inhibited by ADAM, EGFR kinase, and MEK inhibitors. caco2 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15749028-5 2005 IL-8 transiently induced EGFR tyrosine phosphorylation after 5-90 min and this was completely inhibited by ADAM inhibitor. Tyrosine 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15632177-7 2005 This effect was most pronounced with the chemokine, interleukin-8, where alkyl-linked tetrameric cyclitols were essentially inactive unless a spacer of >7 carbon atoms was used. Carbon 158-164 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 15615716-7 2005 Blockade of MEK1 by PD98059 suppresses c-Fos and Fra-1 expression and, thus, affects two counteractive signals for IL-8 mRNA synthesis simultaneously. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15760676-4 2005 However, the regulation of IL-8 production seems to be mediated via a cAMP-independent PKA pathway, since drugs known to enhance cAMP concentrations [PGE2, cholera toxin and dibutyryl cAMP] decrease IL-8 production in irradiated cells by down-regulating NF-kappa B activation in response to UVB radiation. Cyclic AMP 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15760676-4 2005 However, the regulation of IL-8 production seems to be mediated via a cAMP-independent PKA pathway, since drugs known to enhance cAMP concentrations [PGE2, cholera toxin and dibutyryl cAMP] decrease IL-8 production in irradiated cells by down-regulating NF-kappa B activation in response to UVB radiation. Cyclic AMP 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 15760676-1 2005 We have previously demonstrated that treatment of the human keratinocyte cell line NCTC 2544 with a UVB dose equivalent to 1h exposure (100 mJ/cm2) results in a significant increase of IL-8 production. Hydrogen 123-125 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 15760676-4 2005 However, the regulation of IL-8 production seems to be mediated via a cAMP-independent PKA pathway, since drugs known to enhance cAMP concentrations [PGE2, cholera toxin and dibutyryl cAMP] decrease IL-8 production in irradiated cells by down-regulating NF-kappa B activation in response to UVB radiation. Cyclic AMP 70-74 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15760676-4 2005 However, the regulation of IL-8 production seems to be mediated via a cAMP-independent PKA pathway, since drugs known to enhance cAMP concentrations [PGE2, cholera toxin and dibutyryl cAMP] decrease IL-8 production in irradiated cells by down-regulating NF-kappa B activation in response to UVB radiation. Dinoprostone 150-154 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15760676-4 2005 However, the regulation of IL-8 production seems to be mediated via a cAMP-independent PKA pathway, since drugs known to enhance cAMP concentrations [PGE2, cholera toxin and dibutyryl cAMP] decrease IL-8 production in irradiated cells by down-regulating NF-kappa B activation in response to UVB radiation. Dinoprostone 150-154 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 15760676-4 2005 However, the regulation of IL-8 production seems to be mediated via a cAMP-independent PKA pathway, since drugs known to enhance cAMP concentrations [PGE2, cholera toxin and dibutyryl cAMP] decrease IL-8 production in irradiated cells by down-regulating NF-kappa B activation in response to UVB radiation. Cyclic AMP 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15760676-4 2005 However, the regulation of IL-8 production seems to be mediated via a cAMP-independent PKA pathway, since drugs known to enhance cAMP concentrations [PGE2, cholera toxin and dibutyryl cAMP] decrease IL-8 production in irradiated cells by down-regulating NF-kappa B activation in response to UVB radiation. Cyclic AMP 129-133 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 15760676-5 2005 Using PMA (a potent pharmacological activator of PKC) and calphostin C (a specific PKC inhibitor), we demonstrated an up-regulation of IL-8 in NCTC 2544 cells and a down-regulation of the cytokine in UVB-irradiated cells, respectively. Tetradecanoylphorbol Acetate 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 15760676-7 2005 Finally, we concluded that a cAMP-independent PKA activation and a PKC-associated pathway are probably involved in the regulation of UVB-induced IL-8 synthesis in human keratinocytes. Cyclic AMP 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 15795529-4 2005 Competitive inhibition of the IL-8 receptor CXCR2 with the small molecule inhibitor SB225002 resulted in a 45-70% decrease in cervical explant susceptibility to HIV-1 infection. SB 225002 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 15695543-0 2005 Ultrafine carbon particles induce interleukin-8 gene transcription and p38 MAPK activation in normal human bronchial epithelial cells. Carbon 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 15679717-4 2005 RESULTS: The release of GM-CSF, RANTES and IL-8 in ISC was significantly reduced by BDP plus salbutamol or formoterol as compared with either drug alone (P < 0.0001). Formoterol Fumarate 107-117 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 15679717-4 2005 RESULTS: The release of GM-CSF, RANTES and IL-8 in ISC was significantly reduced by BDP plus salbutamol or formoterol as compared with either drug alone (P < 0.0001). Beclomethasone 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 15679717-4 2005 RESULTS: The release of GM-CSF, RANTES and IL-8 in ISC was significantly reduced by BDP plus salbutamol or formoterol as compared with either drug alone (P < 0.0001). Albuterol 93-103 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 15498828-6 2005 IL-8 release was blocked by actinomycin D or cycloheximide, but the inhibitors had no effect on VEGF release, suggesting that IL-8 secretion required de novo synthesis whereas VEGF was secreted from preformed stores. Dactinomycin 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15498828-6 2005 IL-8 release was blocked by actinomycin D or cycloheximide, but the inhibitors had no effect on VEGF release, suggesting that IL-8 secretion required de novo synthesis whereas VEGF was secreted from preformed stores. Cycloheximide 45-58 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15498828-10 2005 These findings suggest that bacteria-derived tripeptides stimulate human PMN to release VEGF and IL-8, which activate endothelial cells and induce angiogenesis by a paracrine feedforward mechanism involving endothelial IL-8 upregulation. tripeptides 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 15498828-10 2005 These findings suggest that bacteria-derived tripeptides stimulate human PMN to release VEGF and IL-8, which activate endothelial cells and induce angiogenesis by a paracrine feedforward mechanism involving endothelial IL-8 upregulation. tripeptides 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 15695543-4 2005 Here, we report that carbonaceous ultrafine particles consisting of synthetic elemental carbon particles (UfCP) markedly increase the expression of IL-8 mRNA and protein in normal human bronchial epithelial (NHBE) cells. carbonaceous 21-33 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 15695543-4 2005 Here, we report that carbonaceous ultrafine particles consisting of synthetic elemental carbon particles (UfCP) markedly increase the expression of IL-8 mRNA and protein in normal human bronchial epithelial (NHBE) cells. Carbon 21-27 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 15695543-8 2005 Additionally, we observed that UfCP exposure induces the phosphorylation and activation of p38 mitogen-activated protein kinase (MAPK) in a biphasic manner and that the inhibition of p38 MAPK activity can block IL-8 mRNA expression induced by UfCP in NHBE cells. ufcp 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 15695543-9 2005 These results demonstrate that UfCP-induced expression of IL-8 involves a transcriptional mechanism and activation of p38 MAPK in NHBE cells. ufcp 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 16142584-7 2005 The highest capacity to simultaneously stimulate IL-8 secretion (quantified by ELISA and by using a multiplexed, particle-based flow cytometric assay) and enhance IL-8 mRNA levels (determined by RT-PCR) was observed with 7beta-hydroxycholesterol and 25-hydroxycholesterol. cholest-5-en-3 beta,7 alpha-diol 221-245 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 16142584-7 2005 The highest capacity to simultaneously stimulate IL-8 secretion (quantified by ELISA and by using a multiplexed, particle-based flow cytometric assay) and enhance IL-8 mRNA levels (determined by RT-PCR) was observed with 7beta-hydroxycholesterol and 25-hydroxycholesterol. cholest-5-en-3 beta,7 alpha-diol 221-245 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 15540988-6 2005 Chemoattractant cytokines [e.g. VEGF (vascular endothelial growth factor), TGF-beta1 (transforming growth factor-beta1) and IL-8] are important regulators of inflammation-induced angiogenesis and are directly modulated by nitric oxide. Nitric Oxide 222-234 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 15564333-7 2005 Treatment of adipose tissue and skeletal muscle with sulfasalazine and BAY 11-7082 significantly inhibited the release of IL-6, IL-8, and TNF-alpha; NF-kappa B p65 DNA-binding activity; and IKK-beta protein expression (P < 0.05, by Newman-Keuls test). Sulfasalazine 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 15564333-7 2005 Treatment of adipose tissue and skeletal muscle with sulfasalazine and BAY 11-7082 significantly inhibited the release of IL-6, IL-8, and TNF-alpha; NF-kappa B p65 DNA-binding activity; and IKK-beta protein expression (P < 0.05, by Newman-Keuls test). 3-(4-methylphenylsulfonyl)-2-propenenitrile 71-82 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 15760531-4 2005 RESULTS: After operation, the contents of IL-6, IL-8, TNF-alpha, CK-MB and cTnI were significantly higher in CCABG group than those before operation and those in OPCABG group, while most of these parameters showed little change in OPCABG group both in operative or postoperative period. ccabg 109-114 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 15901049-6 2005 Additionally, IL-8 was significantly reduced in BP, and ICAM-1 and albumin were present in lower concentrations in BAP. benzylaminopurine 115-118 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 15613411-3 2005 The aim of this study was to describe the temporal and spatial expression of IL-8 in human endometrial endothelial cells (HEEC) in vivo and to compare the in vitro regulation of IL-8 expression by sex steroids in HEEC from women with or without endometriosis. Steroids 201-209 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 15613411-8 2005 The effects of estradiol (5 x 10(-8) m), progesterone (10(-7) m), or both on IL-8 mRNA and protein levels were analyzed by RT-PCR and ELISA, respectively. Estradiol 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15613411-8 2005 The effects of estradiol (5 x 10(-8) m), progesterone (10(-7) m), or both on IL-8 mRNA and protein levels were analyzed by RT-PCR and ELISA, respectively. Progesterone 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15613411-9 2005 Sex steroids reduced the expression of IL-8 mRNA and protein in HEEC from women without endometriosis. Steroids 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 15777258-5 2005 Thiopental and ketamine inhibit the endotoxin-induced TNF-alpha, IL-1 and IL-8 responses and increase IL-10 release in vitro. Thiopental 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15777258-5 2005 Thiopental and ketamine inhibit the endotoxin-induced TNF-alpha, IL-1 and IL-8 responses and increase IL-10 release in vitro. Ketamine 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15585673-5 2005 On the basis of simulated mutation analyses, we hypothesized that this protease resistance is due to disulfide bond-related tertiary folding in IL-8/CXCL8. Disulfides 101-110 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 15585673-5 2005 On the basis of simulated mutation analyses, we hypothesized that this protease resistance is due to disulfide bond-related tertiary folding in IL-8/CXCL8. Disulfides 101-110 C-X-C motif chemokine ligand 8 Homo sapiens 149-154 15823106-0 2005 Predictive value of serum interleukin-8 levels in ovarian cancer patients treated with paclitaxel-containing regimens. Paclitaxel 87-97 C-X-C motif chemokine ligand 8 Homo sapiens 26-39 15823106-1 2005 Previous findings showed that paclitaxel induces interleukin-8 (IL-8) transcription and secretion in ovarian cancer cells in vitro. Paclitaxel 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 15823106-1 2005 Previous findings showed that paclitaxel induces interleukin-8 (IL-8) transcription and secretion in ovarian cancer cells in vitro. Paclitaxel 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 15823106-2 2005 We hypothesized that paclitaxel treatment, which is a standard care for ovarian cancer patients, may increase the secretion of IL-8, resulting in the elevated serum IL-8 levels. Paclitaxel 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 15823106-2 2005 We hypothesized that paclitaxel treatment, which is a standard care for ovarian cancer patients, may increase the secretion of IL-8, resulting in the elevated serum IL-8 levels. Paclitaxel 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 15823106-3 2005 In this study, we investigated the relationship between paclitaxel exposure and IL-8 levels of an ovarian and a breast carcinoma cell line in vitro and serums of patients with ovarian carcinoma. Paclitaxel 56-66 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 15823106-5 2005 However, supernatant levels of IL-8 assessed by enzyme-linked immunosorbent assay before and after treatment with different concentrations of paclitaxel were significantly lower in MCF-7 than in MDAH 2774. Paclitaxel 142-152 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 15823106-8 2005 The basal level of IL-8 after paclitaxel-containing treatment was found to be significantly higher in the serums of patients who had high tumor burden than in patients who had optimal debulking surgery and low tumor burden. Paclitaxel 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 15823106-9 2005 These data strongly suggest that IL-8 may be an important predictive marker for tumor volume as well as sensitivity to paclitaxel. Paclitaxel 119-129 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 15868064-0 2005 Reaction characteristics of a tooth-bleaching agent containing H2O2 and NaF: in vitro study of crystal structure change in treated hydroxyapatite and chemical states of incorporated fluorine. Durapatite 131-145 C-X-C motif chemokine ligand 8 Homo sapiens 63-75 15868064-0 2005 Reaction characteristics of a tooth-bleaching agent containing H2O2 and NaF: in vitro study of crystal structure change in treated hydroxyapatite and chemical states of incorporated fluorine. Fluorine 182-190 C-X-C motif chemokine ligand 8 Homo sapiens 63-75 15868064-1 2005 This in vitro study was performed to elucidate the reaction mechanism of sodium fluoride (NaF), which is added to tooth-bleaching agents to lessen the adverse effect of hydrogen peroxide (H2O2) on teeth. Sodium Fluoride 73-88 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 15868064-1 2005 This in vitro study was performed to elucidate the reaction mechanism of sodium fluoride (NaF), which is added to tooth-bleaching agents to lessen the adverse effect of hydrogen peroxide (H2O2) on teeth. Hydrogen Peroxide 169-186 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 15868064-1 2005 This in vitro study was performed to elucidate the reaction mechanism of sodium fluoride (NaF), which is added to tooth-bleaching agents to lessen the adverse effect of hydrogen peroxide (H2O2) on teeth. Hydrogen Peroxide 188-192 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 15868064-3 2005 In the H2O2/NaF solutions, however, fluorine compounds that could not be identified by X-ray diffraction (XRD) due to the smallness of the products were formed on the surface of the HAP. Hydrogen Peroxide 7-11 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 15868064-3 2005 In the H2O2/NaF solutions, however, fluorine compounds that could not be identified by X-ray diffraction (XRD) due to the smallness of the products were formed on the surface of the HAP. Fluorine 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 15868064-5 2005 In H2O2/NaF solution, DCPD also transformed easily to FHAP and CaF2, which are favorable to the remineralization process on the tooth surface. 2'-deoxycytidine diphosphate 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 8-11 15868064-6 2005 Thus, the mechanism of NaF was elucidated, and its use together with H2O2 for tooth bleaching was proved to be effective. Hydrogen Peroxide 69-73 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 15952644-1 2005 OBJECTIVE: This study was to investigate the effect of crocidolite fibers on IL-8 protein and mRNA levels in A549 cells cultured supernatant and the role of tyrosine kinase inhibitor PD98059 on IL-8 expression. Asbestos, Crocidolite 55-66 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15952644-1 2005 OBJECTIVE: This study was to investigate the effect of crocidolite fibers on IL-8 protein and mRNA levels in A549 cells cultured supernatant and the role of tyrosine kinase inhibitor PD98059 on IL-8 expression. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 183-190 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 15952644-3 2005 RESULTS: After incubating cells with 100 microg/ml of crocidolite, IL-8 protein releasing in supernatant was significantly increased and IL-8 mRNA was also higher than that of control, the differences were statistically significant (P < 0.05), however both IL-8 protein and mRNA was abrogated by pretreating cells with tyrosine kinase inhibitor PD98059. Asbestos, Crocidolite 54-65 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 15952644-3 2005 RESULTS: After incubating cells with 100 microg/ml of crocidolite, IL-8 protein releasing in supernatant was significantly increased and IL-8 mRNA was also higher than that of control, the differences were statistically significant (P < 0.05), however both IL-8 protein and mRNA was abrogated by pretreating cells with tyrosine kinase inhibitor PD98059. Asbestos, Crocidolite 54-65 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 15952644-3 2005 RESULTS: After incubating cells with 100 microg/ml of crocidolite, IL-8 protein releasing in supernatant was significantly increased and IL-8 mRNA was also higher than that of control, the differences were statistically significant (P < 0.05), however both IL-8 protein and mRNA was abrogated by pretreating cells with tyrosine kinase inhibitor PD98059. Asbestos, Crocidolite 54-65 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 15952644-3 2005 RESULTS: After incubating cells with 100 microg/ml of crocidolite, IL-8 protein releasing in supernatant was significantly increased and IL-8 mRNA was also higher than that of control, the differences were statistically significant (P < 0.05), however both IL-8 protein and mRNA was abrogated by pretreating cells with tyrosine kinase inhibitor PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 348-355 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 15952644-4 2005 CONCLUSION: IL-8 was shown as overexpression and could be decreased by PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 71-78 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 15668340-7 2005 Dipyridamole delayed maximal synthesis of interleukin-8 but did not alter cyclooxygenase-2 accumulation. Dipyridamole 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 15804113-11 2005 The results indicate that the expression of cytokines (IL-2, IL-8, IL-10) in EPS can serve as a valuable marker for the diagnosis of CP. eps 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15709756-6 2005 Addition of AlCl(3) and NaF to the reduced double mutant after incubation with stoichiometric MgADP or 200 microM MgADP irreversibly inactivated the steady state ATPase activity with rate constants of 1.5 x10(-2) and 4.1 x 10(-2) min(-1), respectively. Adenosine Diphosphate 94-99 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 15709756-6 2005 Addition of AlCl(3) and NaF to the reduced double mutant after incubation with stoichiometric MgADP or 200 microM MgADP irreversibly inactivated the steady state ATPase activity with rate constants of 1.5 x10(-2) and 4.1 x 10(-2) min(-1), respectively. Adenosine Diphosphate 114-119 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 15699163-6 2005 The presence of clinically relevant heparin concentrations in human whole blood increased LPS-induced production of the proinflammatory cytokine IL-8. Heparin 36-43 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 15652280-5 2005 When CYSST (1mg/ml) was added, the production of tumor necrosis factor-alpha, interleukin (IL)-6, and IL-8 was significantly inhibited about 37, 33.6, and 48%, respectively on phorbol 12-myristate 13-acetate (PMA) plus calcium ionophore A23187-stimulated HMC-1 cells. cysst 5-10 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 15842830-2 2005 METHODS: The renal tubular cells were cultured and exposed to sodium fluoride (NaF) in 1, 5, 7.5, 12.5 mg F-/L level. Sodium Fluoride 62-77 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 15652492-4 2005 Overexpression of human superoxide dismutase (SOD) by adenovirus-mediated gene transfer or addition of exogenous hydrogen peroxide (H(2)O(2)) significantly enhanced TNF-alpha-induced IL-8 mRNA expression. Hydrogen Peroxide 113-130 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 15694463-7 2005 When NHBE were stimulated with PM(2.5-10), PM2.5, and UF PM, in the presence or absence of inhibitors of TLR2 and TLR4 activation, a blocking antibody to TLR2 inhibited production of IL-8, while TLR4 antagonist E5531 or the LPS inhibitor Polymixin B had no effect. E 5531 211-216 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 15709200-14 2005 Furthermore, in Adriamycin-resistant MCF-7 cells highly expressing multidrug resistance gene-1, DHMEQ also exhibited the above capability, including down-regulation of IL-8. Doxorubicin 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 15673867-6 2005 Lidocaine (0.5 mg/mL) decreased IL-1beta (1.89 +/- 0.11 versus 4.16 +/- 1.27 pg/mL; P = 0.009), IL-6 (65.5 +/- 5.14 versus 162 +/- 11.5 pg/mL; P < 0.001), and IL-8 (3869 +/- 785 versus 14,961 +/- 406 pg/mL; P < 0.001) concentrations compared with the control. Lidocaine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 15652235-5 2005 Histamine induced concentration- and time-dependent production of granulocyte-macrophage-colony stimulating factor (GM-CSF), interleukin (IL)-8 and IL-6, which was completely blocked by olopatadine, an H1 antagonist. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 125-143 15652235-5 2005 Histamine induced concentration- and time-dependent production of granulocyte-macrophage-colony stimulating factor (GM-CSF), interleukin (IL)-8 and IL-6, which was completely blocked by olopatadine, an H1 antagonist. Olopatadine Hydrochloride 186-197 C-X-C motif chemokine ligand 8 Homo sapiens 125-143 15494208-3 2005 Both fMLP and IL-8 increased CD38 in supernatants, which was inhibitable with PMSF. Phenylmethylsulfonyl Fluoride 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 15494208-7 2005 The addition of SB20358 blocked the decrease of CD38 on neutrophils and the increase in supernatants induced by fMLP or IL-8, whereas PD98059 did not. Ethyl 2-amino-5-Boc-6,7-dihydro-4H-thieno[3,2-c]pyridine-3-carboxylate 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 15652235-10 2005 PD98059 preferentially inhibited GM-CSF production whereas BAY 11-8702 prevented IL-8 and IL-6 production. bay 11-8702 59-70 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 15709200-14 2005 Furthermore, in Adriamycin-resistant MCF-7 cells highly expressing multidrug resistance gene-1, DHMEQ also exhibited the above capability, including down-regulation of IL-8. dehydroxymethylepoxyquinomicin 96-101 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 15687063-7 2005 In particular, the preinflammatory cytokine interleukin 8 and one of its receptors, chemokine receptor 4, seemed to play important roles in early-stage response to heavy metal exposure and were down-regulated. Metals 170-175 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 15750714-9 2005 CONCLUSIONS: The present data indicate the differential regulation by DLE of the production of TNFalpha, IL-6, and IL-8 cytokines, associated with effects on TLR2 and TLR4 expression and NF-kappaB and cAMP activities. Cyclic AMP 201-205 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15696082-4 2005 OBJECTIVE: We sought to investigate the effect of a 2-week course of oral corticosteroid (methylprednisolone, 40 mg/d) on the expression of CXC chemokines (IL-8 and IFN-gamma-inducible protein 10 [IP-10]) and CC chemokines (eotaxin and monocyte chemotactic proteins [MCPs] 1-4) in endoscopic biopsy specimens of 13 patients with moderate-to-severe asthma. Methylprednisolone 90-108 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 15647850-0 2005 High-dose hydrocortisone reduces expression of the pro-inflammatory chemokines CXCL8 and CXCL10 in SARS coronavirus-infected intestinal cells. Hydrocortisone 10-24 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 15647850-5 2005 High hydrocortisone concentrations (> or =50 microg/ml) completely prevented increased DNA binding activity of AP-1 and NF-kappaB and inhibited up-regulation of CXCL8 and CXCL10, but did not reduce chemokine expression to basal levels. Hydrocortisone 5-19 C-X-C motif chemokine ligand 8 Homo sapiens 164-169 15751881-1 2005 We report 784-nm (1G4 --> 3H5 transition) amplified spontaneous emission (ASE) from Tm3+-doped fluoride (ZrF4-BaF2-LaF3-AlF3-NaF) glass fiber pumped by an 1120-nm fiber laser. ase 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 15585560-6 2005 The increase in IL-8 secretion was inhibited by PD98059, an inhibitor of extracellular signal-regulated kinase 1/2. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15652404-2 2005 Abeta(1-42) (5 microM) applied for 8 h induced the expression and increased the production of the pro-inflammatory cytokines IL-6, IL-1beta, TNF-alpha, the inducible enzyme COX-2 and chemokine IL-8. UNII-042A8N37WH 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 15671221-0 2005 Glutamine modulates LPS-induced IL-8 production through IkappaB/NF-kappaB in human fetal and adult intestinal epithelium. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 15671221-6 2005 Gln supplementation partially prevented the LPS-induced elevation of IL-8 in both cell types. Glutamine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 15698409-0 2005 Differential modulation of interleukin 8 by interleukin 4 and interleukin 10 in HepG2 cells treated with acetaldehyde. Acetaldehyde 105-117 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 15698409-2 2005 The purpose of this work was to study the regulation of IL-8 by IL-10 and IL-4 in HepG2 cells treated with acetaldehyde (Ac). Acetaldehyde 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 15698409-2 2005 The purpose of this work was to study the regulation of IL-8 by IL-10 and IL-4 in HepG2 cells treated with acetaldehyde (Ac). Acetaldehyde 121-123 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 15698409-4 2005 RESULTS: Ac treatment produced an increment in IL-8 induction and secretion that was prevented by IL-4 pretreatment, while IL-10 pretreatment failed to decrease Ac-induced IL-8 production. Acetaldehyde 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 15751881-1 2005 We report 784-nm (1G4 --> 3H5 transition) amplified spontaneous emission (ASE) from Tm3+-doped fluoride (ZrF4-BaF2-LaF3-AlF3-NaF) glass fiber pumped by an 1120-nm fiber laser. tm3+-doped fluoride 87-106 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 15531761-2 2005 We recently demonstrated that glucocorticoids and beta(2)-agonists additively or synergistically suppress tumor necrosis factor-alpha (TNFalpha)-induced production of chemokines eotaxin and interleukin-8 (IL-8), respectively, in human airway smooth muscle (HASM) cells, which may partly explain their combined benefits in asthma. beta(2) 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 190-203 15531761-4 2005 We reported here that the PPARgamma agonists 15-deoxy-Delta(12,14)-PGJ(2) (15d-PGJ(2)) and troglitazone, but not PPARalpha agonist WY-14643, inhibited TNFalpha-induced production of eotaxin and monocyte chemotactic protein-1 (MCP-1) but not IL-8. Troglitazone 91-103 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 15531761-2 2005 We recently demonstrated that glucocorticoids and beta(2)-agonists additively or synergistically suppress tumor necrosis factor-alpha (TNFalpha)-induced production of chemokines eotaxin and interleukin-8 (IL-8), respectively, in human airway smooth muscle (HASM) cells, which may partly explain their combined benefits in asthma. beta(2) 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 15556942-9 2005 IL8 treatment resulted in the increase of cGMP level that was inhibited by the IP(3) receptor blocker but not a protein kinase C inhibitor. Cyclic GMP 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 18969806-5 2005 In addition, the effects of heavy metals (Cu(2+), Cd(2+), Fe(3+)), fluoride (NaF), benzene and dimethylsulphoxide on cholinesterase activities were evaluated. Fluorides 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 15556942-14 2005 These results demonstrate that CD38 is stimulated by sequential activation of IL8 receptor, IP(3)-mediated Ca(2+) rise, and cGMP/protein kinase G and that CD38 plays an essential role in IL8-induced migration of LAK cells. Inositol 1,4,5-Trisphosphate 92-97 C-X-C motif chemokine ligand 8 Homo sapiens 187-190 15588914-3 2005 DON (62.5-500 ng/ml) also significantly upregulated IL-2 and IL-8 production following prestimulation with phorbol myristate acetate and ionomycin. deoxynivalenol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15627478-4 2005 On the contrary, both RSG and TRO significantly potentiated TNF-alpha-induced production of granulocyte/macrophage-colony-stimulating factor, interleukin (IL)-6 and/or IL-8 in these cells. Rosiglitazone 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 15627478-4 2005 On the contrary, both RSG and TRO significantly potentiated TNF-alpha-induced production of granulocyte/macrophage-colony-stimulating factor, interleukin (IL)-6 and/or IL-8 in these cells. Troglitazone 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 15461590-7 2005 Furthermore, overexpression of LPP-1 partially attenuated LPA-induced increases in the intracellular Ca2+ concentration, phosphorylation of IkappaB (inhibitory kappaB) and translocation of NF-kappaB (nuclear factor-kappaB) to the nucleus, and almost completely prevented IL-8 secretion. lysophosphatidic acid 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 271-275 15588914-3 2005 DON (62.5-500 ng/ml) also significantly upregulated IL-2 and IL-8 production following prestimulation with phorbol myristate acetate and ionomycin. Tetradecanoylphorbol Acetate 107-132 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15588914-3 2005 DON (62.5-500 ng/ml) also significantly upregulated IL-2 and IL-8 production following prestimulation with phorbol myristate acetate and ionomycin. Ionomycin 137-146 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15588914-10 2005 In contrast, 15-ADON at 62.5-500 ng/ml and 3-ADON at 625-5000 ng/ml upregulated IL-8 production but FX and NIV had no effect. 15-acetyldeoxynivalenol 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 15588914-10 2005 In contrast, 15-ADON at 62.5-500 ng/ml and 3-ADON at 625-5000 ng/ml upregulated IL-8 production but FX and NIV had no effect. 3-acetyldeoxynivalenol 43-49 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 15588914-12 2005 Although DON shared its capacity to induce apoptosis and potentiate IL-8 production with other 8-ketotrichothecenes, it appeared to be unique in its capacity to upregulate IL-2. deoxynivalenol 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 15588680-6 2005 The production of IL-6 and IL-8 was dose-dependently inhibited by pretreatment with ZST (0.01-1 mg/ml) on IL-1beta and Abeta-stimulated U373MG cells. UNII-042A8N37WH 119-124 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15650393-0 2005 Inhibition of NFkappaB activation and IL-8 expression in human bronchial epithelial cells by acrolein. Acrolein 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 15659119-0 2005 Signal pathways underlying homocysteine-induced production of MCP-1 and IL-8 in cultured human whole blood. Homocysteine 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 15659119-5 2005 CONCLUSION: Hcy-induced MCP-1 and IL-8 production is mediated by activated signaling pathways such as PKC, CaM, MAPK, and NF-kappaB. Homocysteine 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 15696447-13 2005 Serum IL-8 levels correlated significantly with FE UA (P < 0.001; r = 0.785) and inversely with serum UA level (P = 0.044; r = -0.509); neither IL-6 nor TNF-alpha level showed such correlations. Uric Acid 51-53 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 15650393-4 2005 Cell exposure to acrolein dose-dependently suppressed IL-8 mRNA levels in HBE1 cells (26, 40, and 79% at 5, 10, and 25 microM acrolein concentrations, respectively) and resulted in corresponding decreases in IL-8 production. Acrolein 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 15650393-4 2005 Cell exposure to acrolein dose-dependently suppressed IL-8 mRNA levels in HBE1 cells (26, 40, and 79% at 5, 10, and 25 microM acrolein concentrations, respectively) and resulted in corresponding decreases in IL-8 production. Acrolein 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 15650393-7 2005 In summary, our results demonstrate that acrolein can suppress inflammatory processes in the airways by inhibiting epithelial IL-8 production through direct or indirect inhibitory effects on NFkappaB activation. Acrolein 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 16179748-1 2005 Homocysteine, cytokines (IL-18, IL-6, IL-8) are involved in vascular inflammation and coronary artery disease. Homocysteine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 15539624-11 2005 Importantly, IL-8 significantly induced CRP release in PHHs by 58.675+/-19.1-fold, which was blockable by LY333531. ruboxistaurin 106-114 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 15641067-4 2005 This study was undertaken to test the hypothesis that IL-8 promotes chondrocyte hypertrophy by modulating chondrocyte PiT-1 expression and sodium-dependent Pi uptake, and to assess differential roles in this activity. Sodium 139-145 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 15641067-8 2005 IL-8, but not IL-1 or the CXCR2 ligand growth-related oncogene alpha, induced PiT-1 expression and increased sodium-dependent Pi uptake by >40% in chondrocytes. Sodium 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15641067-9 2005 The sodium/phosphate cotransport inhibitor phosphonoformic acid blocked IL-8-induced chondrocyte hypertrophic differentiation. Foscarnet 43-63 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 15641067-12 2005 CONCLUSION: Our results link low-grade IL-8-mediated cartilaginous inflammation in OA to altered chondrocyte differentiation and disease progression through PiT-1 expression and sodium-dependent Pi uptake mediated by CXCR1 signaling. Sodium 178-184 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 16179748-2 2005 Homocysteine influences endothelial IL-6 and IL-8 cytokine expression and release, however, an association between homocysteine and IL-18 has not been previously investigated in endothelial/smooth muscle cells and or in coronary artery disease. Homocysteine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 15843228-11 2005 Initial IL-8 serum levels were significantly higher in the hydrocortisone group up to 12 h after study entry, and significantly decreased from 715 to 17 pg/mL at the end of the observation period. Hydrocortisone 59-73 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 15894821-6 2005 However, following transfection with a functional mutant of TLR4 (C3H/HeJ, TLR4 Dicd) or addition of anti-human TLR4 mAb, IL-8 expression was obviously decreased, NF-kappaB activity in cells remarkably inhibited, and the adhesion force of monocyte significantly reduced. dicd 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15606618-6 2005 IkappaB-alpha phosphorylation inhibitor, BAY 11-7082, and p38 MAPK inhibitor, SB 203580 could decrease the release of IL-8, IP-10 and MCP-1 in the coculture. 3-(4-methylphenylsulfonyl)-2-propenenitrile 41-52 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 15606618-6 2005 IkappaB-alpha phosphorylation inhibitor, BAY 11-7082, and p38 MAPK inhibitor, SB 203580 could decrease the release of IL-8, IP-10 and MCP-1 in the coculture. SB 203580 78-87 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 15617523-0 2005 Muramyldipeptide and diaminopimelic acid-containing desmuramylpeptides in combination with chemically synthesized Toll-like receptor agonists synergistically induced production of interleukin-8 in a NOD2- and NOD1-dependent manner, respectively, in human monocytic cells in culture. Diaminopimelic Acid 21-40 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 15617523-0 2005 Muramyldipeptide and diaminopimelic acid-containing desmuramylpeptides in combination with chemically synthesized Toll-like receptor agonists synergistically induced production of interleukin-8 in a NOD2- and NOD1-dependent manner, respectively, in human monocytic cells in culture. desmuramylpeptides 52-70 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 15617523-2 2005 We found marked synergistic IL-8 secretion induced by MDP or DAP-containing DMP in combination with synthetic TLR agonists in THP-1 cells. Diaminopimelic Acid 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 15617523-2 2005 We found marked synergistic IL-8 secretion induced by MDP or DAP-containing DMP in combination with synthetic TLR agonists in THP-1 cells. dmp 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 15617523-3 2005 Suppression of the mRNA expression of nucleotide-binding oligomerization domain (NOD)1 and NOD2 by RNA interference specifically inhibited the synergistic IL-8 secretion induced by DMP and MDP with these TLR agonists respectively. dmp 181-184 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 15617523-3 2005 Suppression of the mRNA expression of nucleotide-binding oligomerization domain (NOD)1 and NOD2 by RNA interference specifically inhibited the synergistic IL-8 secretion induced by DMP and MDP with these TLR agonists respectively. Acetylmuramyl-Alanyl-Isoglutamine 189-192 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 15617523-4 2005 In accordance with the above results, enhanced IL-8 mRNA expression and the activation of nuclear factor (NF)-kappaB induced by MDP or DMP in combination with synthetic TLR agonists were markedly suppressed in NOD2- and NOD1-silenced cells respectively. dmp 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 15843228-15 2005 Starting S-100B, IL-8 and PMN elastase values of the hydrocortisone group were within the ranges already known in patients with out-of-hospital cardiac arrest or severe traumatic brain injury. Hydrocortisone 53-67 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 15843228-16 2005 Stress doses of hydrocortisone resulted in a significant reduction in IL-8 serum, but not in S-100B serum and PMN elastase plasma concentrations in patients with hyperdynamic septic shock. Hydrocortisone 16-30 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 17532680-7 2005 Furthermore, treatment with NAC 1200 mg/day was more efficacious than NAC 600 mg/day in reducing IL-8 levels and difficulty of expectoration, while the two active regimens had similar beneficial effects on lung function and other clinical outcomes (cough intensity and frequency, and lung auscultation). Acetylcysteine 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 17532680-7 2005 Furthermore, treatment with NAC 1200 mg/day was more efficacious than NAC 600 mg/day in reducing IL-8 levels and difficulty of expectoration, while the two active regimens had similar beneficial effects on lung function and other clinical outcomes (cough intensity and frequency, and lung auscultation). Acetylcysteine 70-73 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 15618178-6 2005 Northern blot analyses after the addition of the transcriptional inhibitor actinomycin D revealed increased IL-8 mRNA stability in THP-1 cells treated with Stx1 or Stx1 plus LPS. Dactinomycin 75-88 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 16280061-13 2005 There were significant negative correlations between the PaO2/FiO2 ratio and blood levels of NE and IL-8. pao2 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 16280061-13 2005 There were significant negative correlations between the PaO2/FiO2 ratio and blood levels of NE and IL-8. fio2 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 16280061-15 2005 The mean blood levels of plasminogen activator inhibitor-1, NE, and IL-8 were significantly decreased from 48 hours after DHP-PMX treatment. dhp-pmx 122-129 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 16280061-17 2005 Improvement in the PaO2/FiO2 ratio appeared to be related to the decreases in blood NE and IL-8 levels. pao2 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 16280061-17 2005 Improvement in the PaO2/FiO2 ratio appeared to be related to the decreases in blood NE and IL-8 levels. fio2 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 14963719-5 2005 In both NS and betamethasone patients, the levels of IL-1beta and IL-8 had significantly decreased by the 3rd and 2nd weeks after therapy, respectively. Betamethasone 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 15582208-8 2005 Cytotoxicity in CEPI mainly correlated with presence and concentrations of surfactants, and IL-8 release to clinical signs and/or glycol and sodium lactate concentrations. Sodium Lactate 141-155 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 15675582-0 2005 [Phase I study of the combination of nedaplatin (NED), adriamycin (ADM), and 5-fluorouracil (5-FU) (NAF) for treatment of unresectable advanced esophageal cancer]. Fluorouracil 77-91 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 15675582-0 2005 [Phase I study of the combination of nedaplatin (NED), adriamycin (ADM), and 5-fluorouracil (5-FU) (NAF) for treatment of unresectable advanced esophageal cancer]. Fluorouracil 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 15618163-9 2005 The upregulation of ICAM-1, IL-6, and IL-8 was completely inhibited by pretreating the cells with an NF-kappaB activation inhibitor, l-1-tosylamido-2-phenylethyl chloromethyl ketone. Tosylphenylalanyl Chloromethyl Ketone 133-181 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 16076033-14 2005 Nevertheless, the impact of catecholamines on IL-8 synthesis and expression of CD15, CD44, and CD54 is limited. Catecholamines 28-42 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 15611265-0 2005 Inhibition of human neutrophil IL-8 production by hydrogen peroxide and dysregulation in chronic granulomatous disease. Hydrogen Peroxide 50-67 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 16435585-5 2005 The amount of tumor necrosis factor (TNF)-alpha, interleukin (IL)-1alpha, IL-1beta, IL-6, and IL-8 in PBMC culture supernatant was significantly increased in the lipopolysaccaride (LPS)- or desferrioxamine (DFX)-treated cells compared with unstimulated cells. lipopolysaccaride 162-179 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16435585-7 2005 Also, DCWGG inhibited TNF-alpha, IL-1alpha, IL-beta, IL-6, and IL-8 production-induced DFX in dose-dependent manner. Deferoxamine 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 16173061-3 2005 Cells overexpressing interleukin 10 suppressed the pro-inflammatory cytokines interleukin 8 and interleukin 6 following exposure to 50-300 microM sulfur mustard. Mustard Gas 146-160 C-X-C motif chemokine ligand 8 Homo sapiens 78-91 15654981-0 2005 Eicosapentaenoic acid and docosahexaenoic acid reduce UVB- and TNF-alpha-induced IL-8 secretion in keratinocytes and UVB-induced IL-8 in fibroblasts. Eicosapentaenoic Acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 15654981-6 2005 In keratinocytes, EPA and DHA were shown to reduce basal secretion of IL-8 by 66% and 63%, respectively (p<0.05), and UVB-induced levels by 66% and 65% at 48 h after 100 mJ per cm2, respectively, (p<0.01). Eicosapentaenoic Acid 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 15611265-5 2005 Moreover, normal neutrophils treated with catalase (H(2)O(2) scavenger) or diphenyleneiodonium chloride (NADPH oxidase inhibitor) exhibit IL-8 responses comparable to those of CGD neutrophils. Hydrogen Peroxide 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 15654981-6 2005 In keratinocytes, EPA and DHA were shown to reduce basal secretion of IL-8 by 66% and 63%, respectively (p<0.05), and UVB-induced levels by 66% and 65% at 48 h after 100 mJ per cm2, respectively, (p<0.01). Docosahexaenoic Acids 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 15654981-0 2005 Eicosapentaenoic acid and docosahexaenoic acid reduce UVB- and TNF-alpha-induced IL-8 secretion in keratinocytes and UVB-induced IL-8 in fibroblasts. Eicosapentaenoic Acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 15654981-0 2005 Eicosapentaenoic acid and docosahexaenoic acid reduce UVB- and TNF-alpha-induced IL-8 secretion in keratinocytes and UVB-induced IL-8 in fibroblasts. Docosahexaenoic Acids 26-46 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 15654981-8 2005 In addition, TNF-alpha-induced IL-8 secretion by keratinocytes was reduced by 54% and 42%, respectively, by EPA and DHA (p<0.001). Eicosapentaenoic Acid 108-111 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 15654981-0 2005 Eicosapentaenoic acid and docosahexaenoic acid reduce UVB- and TNF-alpha-induced IL-8 secretion in keratinocytes and UVB-induced IL-8 in fibroblasts. Docosahexaenoic Acids 26-46 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 15611265-5 2005 Moreover, normal neutrophils treated with catalase (H(2)O(2) scavenger) or diphenyleneiodonium chloride (NADPH oxidase inhibitor) exhibit IL-8 responses comparable to those of CGD neutrophils. diphenyleneiodonium 75-103 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 15654981-8 2005 In addition, TNF-alpha-induced IL-8 secretion by keratinocytes was reduced by 54% and 42%, respectively, by EPA and DHA (p<0.001). Docosahexaenoic Acids 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 15611265-6 2005 Addition of hydrogen peroxide or an H(2)O(2)-generating system suppresses the sustained IL-8 mRNA and increased protein production observed in CGD neutrophils. Hydrogen Peroxide 12-29 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 15611265-6 2005 Addition of hydrogen peroxide or an H(2)O(2)-generating system suppresses the sustained IL-8 mRNA and increased protein production observed in CGD neutrophils. Hydrogen Peroxide 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 16218490-6 2005 Finally, TZDs induce synoviocyte apoptosis and reduce secretion of TNFalpha, IL-6 and IL-8 in synoviocyte from rheumatoid arthritis patients. Thiazolidinediones 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 15454116-0 2004 Glycyrrhizin and related compounds down-regulate production of inflammatory chemokines IL-8 and eotaxin 1 in a human lung fibroblast cell line. Glycyrrhizic Acid 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 16356023-18 2005 Montelukast treatment decreased serum and sputum levels of eosinophil cationic protein and interleukin-8 (IL-8), decreased sputum levels of myeloperoxidase, and increased serum and sputum levels of IL-10 (p < 0.001 for all) compared with placebo. montelukast 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 16356023-18 2005 Montelukast treatment decreased serum and sputum levels of eosinophil cationic protein and interleukin-8 (IL-8), decreased sputum levels of myeloperoxidase, and increased serum and sputum levels of IL-10 (p < 0.001 for all) compared with placebo. montelukast 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 15939312-7 2005 Fluticasone propionate was able to suppress IL-1beta induced IL-8 protein and promoter activation, using both a -1481 bp fragment and a -133 bp fragment, indicating that the glucocorticoid response element found at -330 bp was not required for fluticasone mediated suppression of IL-8 promoter activation. Fluticasone 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15939312-7 2005 Fluticasone propionate was able to suppress IL-1beta induced IL-8 protein and promoter activation, using both a -1481 bp fragment and a -133 bp fragment, indicating that the glucocorticoid response element found at -330 bp was not required for fluticasone mediated suppression of IL-8 promoter activation. Fluticasone 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 280-284 15939312-7 2005 Fluticasone propionate was able to suppress IL-1beta induced IL-8 protein and promoter activation, using both a -1481 bp fragment and a -133 bp fragment, indicating that the glucocorticoid response element found at -330 bp was not required for fluticasone mediated suppression of IL-8 promoter activation. Fluticasone 244-255 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15939314-7 2005 RESULTS: Salbutamol at concentrations of 10(-4), 10(-5) and 10(-9) M inhibited IL-8, elastase release and migration of neutrophils in an inverse bell-shaped concentration-response manner. Albuterol 9-19 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 15939314-10 2005 CONCLUSIONS: Salbutamol inhibits neutrophil migration and IL-8 and elastase release in a concentration-dependent manner. Albuterol 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 58-75 15893134-8 2005 In the process of the search for such a unique anti-hypertensive drug, we have recently found that azelnidipine, a newly developed and commercially used long-acting dihydropyridine-based calcium antagonist (DHP), inhibited TNF-alpha-induced activator protein-1 activation and interleukin-8 expression in human umbilical vein endothelial cells by suppressing NADPH oxidase-mediated reactive oxygen species generation. azelnidipine 99-111 C-X-C motif chemokine ligand 8 Homo sapiens 276-289 16044843-5 2005 Evidence was obtained showing that after a 2-dyas exposure at room temperature in presence of floride NaF, Aluminum foil liberated nearly 1 mg/l of Aluminum, compared with less than 0.04 mg/l in absence of fluoride. Aluminum 107-115 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 16044843-6 2005 There is reason to believe that in experiments with ascorbic acid NaF prevents the oxidation of ascorbic acid. Ascorbic Acid 52-65 C-X-C motif chemokine ligand 8 Homo sapiens 66-69 15489227-0 2004 Constitutive and interleukin-1-inducible phosphorylation of p65 NF-{kappa}B at serine 536 is mediated by multiple protein kinases including I{kappa}B kinase (IKK)-{alpha}, IKK{beta}, IKK{epsilon}, TRAF family member-associated (TANK)-binding kinase 1 (TBK1), and an unknown kinase and couples p65 to TATA-binding protein-associated factor II31-mediated interleukin-8 transcription. Serine 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 353-366 15489227-10 2004 Collectively, our results provide evidence for at least five kinases that converge on Ser-536 of p65 and a novel function for this phosphorylation site in the recruitment of components of the basal transcriptional machinery to the interleukin-8 promoter. Serine 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 231-244 15454116-6 2004 18alpha,beta-GL inhibited IL-8 dose-dependently and inhibited eotaxin 1 slightly. 18alpha 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 15604281-6 2004 Complementary DNA microarray expression profiling allowed us to identify a subset of genes specifically regulated by tamoxifen and CC-8490, and not by other apoptotic stimuli, including nuclear factor (NF)-kappaB with its target genes IEX-3, SOD2, IL6, and IL8. Tamoxifen 117-126 C-X-C motif chemokine ligand 8 Homo sapiens 257-260 15454116-6 2004 18alpha,beta-GL inhibited IL-8 dose-dependently and inhibited eotaxin 1 slightly. Glycyrrhizic Acid 8-15 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 15530425-4 2004 METHODS AND RESULTS: AngII-induced upregulation of IL-8 and MCP-1 protein and RNA in monocytes was inhibited by the AT1R-blocker losartan, but not by the AT2R-blocker PD 123.319. Losartan 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 15585881-7 2004 Unexpectedly, both ADP and ATP inhibited the generation of TNF-alpha in response to the TLR2 ligand, peptidoglycan, and blocked the production of TNF-alpha, IL-8, and MIP-1beta in response to leukotriene D(4). Adenosine Diphosphate 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 15585881-7 2004 Unexpectedly, both ADP and ATP inhibited the generation of TNF-alpha in response to the TLR2 ligand, peptidoglycan, and blocked the production of TNF-alpha, IL-8, and MIP-1beta in response to leukotriene D(4). Adenosine Triphosphate 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 15530425-5 2004 Ramiprilat dose-dependently suppressed AngII-induced upregulation of IL-8 and MCP-1. ramiprilat 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 15530425-8 2004 In addition, ramiprilat downregulated NF-kappaB activity and thereby reduced the AngII-induced release of IL-8 and MCP-1 in monocytes. ramiprilat 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 15345720-4 2004 Based on high sequence similarity to the determined structures of the Nogo-receptor ectodomain and the intermolecular complex of the Interleukin-8 ligand (IL8) and the N-terminal peptide of the IL8 receptor (IL8RA), the hypothesis was developed that portions of the intramolecular components, Cysteine-box-2 and Cysteine-box-3, of the GPHR ectodomain interact and localize at the interface between ectodomain and serpentine domain. Cysteine 293-301 C-X-C motif chemokine ligand 8 Homo sapiens 133-153 15568848-1 2004 Hydroxide adsorption on the (111), (110), and (100) faces of silver electrodes from mixed NaOH/NaF solution is studied using cyclic voltammetry and in situ second harmonic generation (SHG). hydroxide ion 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 15345720-4 2004 Based on high sequence similarity to the determined structures of the Nogo-receptor ectodomain and the intermolecular complex of the Interleukin-8 ligand (IL8) and the N-terminal peptide of the IL8 receptor (IL8RA), the hypothesis was developed that portions of the intramolecular components, Cysteine-box-2 and Cysteine-box-3, of the GPHR ectodomain interact and localize at the interface between ectodomain and serpentine domain. Cysteine 293-301 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 15345720-4 2004 Based on high sequence similarity to the determined structures of the Nogo-receptor ectodomain and the intermolecular complex of the Interleukin-8 ligand (IL8) and the N-terminal peptide of the IL8 receptor (IL8RA), the hypothesis was developed that portions of the intramolecular components, Cysteine-box-2 and Cysteine-box-3, of the GPHR ectodomain interact and localize at the interface between ectodomain and serpentine domain. Cysteine 293-301 C-X-C motif chemokine ligand 8 Homo sapiens 194-197 15345720-4 2004 Based on high sequence similarity to the determined structures of the Nogo-receptor ectodomain and the intermolecular complex of the Interleukin-8 ligand (IL8) and the N-terminal peptide of the IL8 receptor (IL8RA), the hypothesis was developed that portions of the intramolecular components, Cysteine-box-2 and Cysteine-box-3, of the GPHR ectodomain interact and localize at the interface between ectodomain and serpentine domain. Cysteine 312-320 C-X-C motif chemokine ligand 8 Homo sapiens 133-153 15345720-4 2004 Based on high sequence similarity to the determined structures of the Nogo-receptor ectodomain and the intermolecular complex of the Interleukin-8 ligand (IL8) and the N-terminal peptide of the IL8 receptor (IL8RA), the hypothesis was developed that portions of the intramolecular components, Cysteine-box-2 and Cysteine-box-3, of the GPHR ectodomain interact and localize at the interface between ectodomain and serpentine domain. Cysteine 312-320 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 15345720-4 2004 Based on high sequence similarity to the determined structures of the Nogo-receptor ectodomain and the intermolecular complex of the Interleukin-8 ligand (IL8) and the N-terminal peptide of the IL8 receptor (IL8RA), the hypothesis was developed that portions of the intramolecular components, Cysteine-box-2 and Cysteine-box-3, of the GPHR ectodomain interact and localize at the interface between ectodomain and serpentine domain. Cysteine 312-320 C-X-C motif chemokine ligand 8 Homo sapiens 194-197 15577845-10 2004 PGE(2) , EP2, or EP3 agonists reduced TNF-alpha-induced CCL27 secretion and mRNA levels in parallel to NF-kappaB activity and CCL2, CCL5, CXCL8, and CXCL10 mRNA levels. Prostaglandins E 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 138-143 15731299-9 2004 We present evidence for direct and/or indirect roles of steroid hormones on the expression of chemotactic cytokines (interleukin-8 and monocyte chemotactic protein-1) and on the survival versus apoptosis of resident endometrial cells (stromal, epithelial, and endothelial cells) and nonresident cells (leukocytes). Steroids 56-72 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 15731315-10 2004 The addition of the anti-inflammatory steroid, dexamethasone, significantly reduced the LPS-mediated increase in levels of IL-8 in SCTs. Steroids 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 15731315-10 2004 The addition of the anti-inflammatory steroid, dexamethasone, significantly reduced the LPS-mediated increase in levels of IL-8 in SCTs. Dexamethasone 47-60 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 15548807-10 2004 CONCLUSION: Plasma levels of IL-8 are elevated during the acute phase of NAION, but not IL-6 and TNF-alpha. naion 73-78 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 15456740-9 2004 However, H2O2, tumor necrosis factor-alpha (TNF-alpha), and IL-1beta significantly increased NF-kappaB activation and expression of IL-8 compared with control cells. Hydrogen Peroxide 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 15477226-8 2004 IL-8-induced chemotaxis was inhibited in a sexually dimorphic manner by isoprenaline, which also stimulated release of a mediator from neutrophils that induced chemotaxis, that was inhibited by anti-CXCR2 antibodies. Isoproterenol 72-84 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15654514-4 2004 RESULTS: HMC-1 produced substantial amounts of GM-CSF and IL-8 and smaller amounts of TNF-alpha, IL-4 and IL-6 after being stimulated with PMA together with A23187. Tetradecanoylphorbol Acetate 139-142 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 15619426-3 2004 Heat, formalin or protease treatment of F. nucleatum cells attenuated the IL-8 mRNA up-regulation. Formaldehyde 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15610518-0 2004 All-trans-retinoic acid induces interleukin-8 via the nuclear factor-kappaB and p38 mitogen-activated protein kinase pathways in normal human keratinocytes. Tretinoin 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 15610518-3 2004 To test this hypothesis, we investigated whether all-trans-retinoic acid (ATRA) induced IL-8 production in normal human keratinocytes. Tretinoin 49-72 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 15610518-3 2004 To test this hypothesis, we investigated whether all-trans-retinoic acid (ATRA) induced IL-8 production in normal human keratinocytes. Tretinoin 74-78 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 15610518-4 2004 Stimulation with 10(-7) M ATRA enhanced IL-8 mRNA expression and induced IL-8 production. Tretinoin 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 15610518-4 2004 Stimulation with 10(-7) M ATRA enhanced IL-8 mRNA expression and induced IL-8 production. Tretinoin 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 15610518-5 2004 We also studied the intracellular signaling mechanisms of ATRA-induced IL-8 production in keratinocytes. Tretinoin 58-62 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 15610518-7 2004 Introduction of a dominant-negative mutant of IkappaBalpha completely abolished ATRA-induced IL-8 production, which indicates that this process is NF-kappaB-dependent. Tretinoin 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 15610518-9 2004 ATRA phosphorylated the p38 MAPK, and SB202180 inhibited ATRA-induced IL-8 production, which indicates that the p38 MAPK is also involved in ATRA-induced IL-8 production. Tretinoin 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 15610518-9 2004 ATRA phosphorylated the p38 MAPK, and SB202180 inhibited ATRA-induced IL-8 production, which indicates that the p38 MAPK is also involved in ATRA-induced IL-8 production. sb202180 38-46 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 15610518-9 2004 ATRA phosphorylated the p38 MAPK, and SB202180 inhibited ATRA-induced IL-8 production, which indicates that the p38 MAPK is also involved in ATRA-induced IL-8 production. sb202180 38-46 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 15610518-9 2004 ATRA phosphorylated the p38 MAPK, and SB202180 inhibited ATRA-induced IL-8 production, which indicates that the p38 MAPK is also involved in ATRA-induced IL-8 production. Tretinoin 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 15610518-9 2004 ATRA phosphorylated the p38 MAPK, and SB202180 inhibited ATRA-induced IL-8 production, which indicates that the p38 MAPK is also involved in ATRA-induced IL-8 production. Tretinoin 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 15610518-9 2004 ATRA phosphorylated the p38 MAPK, and SB202180 inhibited ATRA-induced IL-8 production, which indicates that the p38 MAPK is also involved in ATRA-induced IL-8 production. Tretinoin 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 15610518-9 2004 ATRA phosphorylated the p38 MAPK, and SB202180 inhibited ATRA-induced IL-8 production, which indicates that the p38 MAPK is also involved in ATRA-induced IL-8 production. Tretinoin 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 15496610-8 2004 Mutation of the IL-8 promoter NF-kappa B site abolished aspirate-induced IL-8 transcription. aspirate 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15610518-10 2004 In summary, ATRA induces IL-8 production in both NF-kappaB- and p38 MAPK-dependent manners in normal human keratinocytes. Tretinoin 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 15569263-6 2004 Curcumin abrogated Abeta1-40-induced expression of cytokines (TNF-alpha and IL-1beta) and chemokines (MIP-1beta, MCP-1 and IL-8) in both peripheral blood monocytes and THP-1 cells. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 15496610-8 2004 Mutation of the IL-8 promoter NF-kappa B site abolished aspirate-induced IL-8 transcription. aspirate 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 15528384-4 2004 Moreover, the NF-kappaB inhibitors pyrrolidinedithiocarbamate, dexamethasone, or sulfasalazine were found to prevent CXCL8 production by sPLA(2)-IB in human neutrophils. pyrrolidine dithiocarbamic acid 35-61 C-X-C motif chemokine ligand 8 Homo sapiens 117-122 15496611-6 2004 IL-1 beta, IL-6, IL-8 and TNF-alpha were significantly associated with lactate/choline in the DGN (p = 0.03, 0.02, 0.03, and 0.01 respectively), but not in the WS (all p > 0.1). Lactic Acid 71-78 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 15496611-6 2004 IL-1 beta, IL-6, IL-8 and TNF-alpha were significantly associated with lactate/choline in the DGN (p = 0.03, 0.02, 0.03, and 0.01 respectively), but not in the WS (all p > 0.1). Choline 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 15545821-1 2004 Several CXC-chemokines, of which interleukin (IL)-8 is the prototype, are potent neutrophil chemotactic and activating cytokines, inducing the secretion of granule proteins and the generation of reactive oxygen intermediates that may cause tissue damage and amplify inflammatory responses. reactive oxygen intermediates 195-224 C-X-C motif chemokine ligand 8 Homo sapiens 33-51 15355994-10 2004 Importantly, using chromatin immunoprecipitation, we show that impaired interaction between GR and p65 with RU486 leads to reduced recruitment of the GR to the NF-kappaB-responsive region of the interleukin-8 promoter, again in contrast to dexamethasone that significantly increased GR binding. Dexamethasone 240-253 C-X-C motif chemokine ligand 8 Homo sapiens 195-208 15331599-6 2004 We also studied the results of cPLA2 activation by epidermal growth factor (EGF) and calcium ionophore (A23187) on IL-8 and COX-2 reporter gene activity, mRNA level, and protein synthesis. Calcium 85-92 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15331599-6 2004 We also studied the results of cPLA2 activation by epidermal growth factor (EGF) and calcium ionophore (A23187) on IL-8 and COX-2 reporter gene activity, mRNA level, and protein synthesis. Calcimycin 104-110 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15331599-9 2004 Methyl arachidonyl fluorophosphate, a cPLA2 inhibitor, inhibited the effect of A23187 and of EGF on both IL-8 and COX-2 reporter gene activity, steady state levels of IL-8 and COX-2 mRNA, and IL-8 and COX-2 protein expression. (5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenyl methyl phosphorofluoridate 0-34 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 15331599-9 2004 Methyl arachidonyl fluorophosphate, a cPLA2 inhibitor, inhibited the effect of A23187 and of EGF on both IL-8 and COX-2 reporter gene activity, steady state levels of IL-8 and COX-2 mRNA, and IL-8 and COX-2 protein expression. (5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenyl methyl phosphorofluoridate 0-34 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 15331599-9 2004 Methyl arachidonyl fluorophosphate, a cPLA2 inhibitor, inhibited the effect of A23187 and of EGF on both IL-8 and COX-2 reporter gene activity, steady state levels of IL-8 and COX-2 mRNA, and IL-8 and COX-2 protein expression. (5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenyl methyl phosphorofluoridate 0-34 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 15331599-9 2004 Methyl arachidonyl fluorophosphate, a cPLA2 inhibitor, inhibited the effect of A23187 and of EGF on both IL-8 and COX-2 reporter gene activity, steady state levels of IL-8 and COX-2 mRNA, and IL-8 and COX-2 protein expression. Calcimycin 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 15331599-9 2004 Methyl arachidonyl fluorophosphate, a cPLA2 inhibitor, inhibited the effect of A23187 and of EGF on both IL-8 and COX-2 reporter gene activity, steady state levels of IL-8 and COX-2 mRNA, and IL-8 and COX-2 protein expression. Calcimycin 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 15331599-9 2004 Methyl arachidonyl fluorophosphate, a cPLA2 inhibitor, inhibited the effect of A23187 and of EGF on both IL-8 and COX-2 reporter gene activity, steady state levels of IL-8 and COX-2 mRNA, and IL-8 and COX-2 protein expression. Calcimycin 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 15331599-10 2004 Small inhibitory RNAs directed against PPAR-gamma1 and -gamma2 blunted the effect of A23187 and of EGF on IL-8 and COX-2 protein expression. Calcimycin 85-91 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 15331599-11 2004 Moreover small inhibitory RNAs directed against cPLA2 decreased the effect of A23187 and EGF on IL-8 and COX-2 protein expression. Calcimycin 78-84 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 15476283-5 2004 Curcumin decreased the expression of NF-kappaB-regulated gene products, including cyclooxygenase-2 (as assessed using immunoblot analysis), prostaglandin E2, and interleukin-8 (as assessed using an enzyme-linked immunoassay), all of which have been implicated in the growth and invasiveness of pancreatic carcinoma. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 15584975-3 2004 For instance, elevated seric levels of IL-8 are a common feature in DHF patients. seric 23-28 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 15364949-6 2004 ROS could indeed be detected in IL-8-stimulated beta-arrestin 1/2 knockout cells, and cytoplasmic Rac was translocated to the membrane fraction, which is a prerequisite for oxidant formation. ros 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 15364949-7 2004 The oxidative burst induced cell death within 6 h of IL-8 stimulation of these cells, which could be prevented in the presence of DPI. diphenyleneiodonium 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 15528377-7 2004 Ethanol, at concentrations within the range found in human blood after acute exposure and below the levels that induce cytotoxicity (0.1-0.5%), did not induce endothelial cell activation, but significantly inhibited TNF-mediated endothelial cell activation, as measured by adhesion molecule (E-selectin, ICAM-1, VCAM-1) expression and chemokine (IL-8, MCP-1, RANTES) production and leukocyte adhesion in vitro. Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 346-350 15528384-4 2004 Moreover, the NF-kappaB inhibitors pyrrolidinedithiocarbamate, dexamethasone, or sulfasalazine were found to prevent CXCL8 production by sPLA(2)-IB in human neutrophils. Dexamethasone 63-76 C-X-C motif chemokine ligand 8 Homo sapiens 117-122 15528384-4 2004 Moreover, the NF-kappaB inhibitors pyrrolidinedithiocarbamate, dexamethasone, or sulfasalazine were found to prevent CXCL8 production by sPLA(2)-IB in human neutrophils. Sulfasalazine 81-94 C-X-C motif chemokine ligand 8 Homo sapiens 117-122 15586558-6 2004 Macrolides inhibit the production of many proinflammatory cytokines, such as interleukin (IL)-1, IL-6, IL-8, and tumor necrosis factor-alpha, perhaps by suppressing the transcription factor nuclear factor-kappaB or activator protein-1. Macrolides 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 103-140 15586558-7 2004 Inhibition of cytokine production has been seen in vitro and also in bronchoalveolar lavage fluid, which contains less IL-8 and fewer neutrophils after treatment with macrolides. Macrolides 167-177 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 15528909-1 2004 The objective of this research was to evaluate the anticaries effectiveness of a low-dose (500 ppm F, low-NaF) sodium fluoride dentifrice, a high-dose (2,800 ppm F, high-NaF) sodium fluoride dentifrice and an experimental 0.454% stabilized stannous fluoride (1,100 ppm F) with sodium hexametaphosphate (SnF2-HMP) dentifrice, each relative to a standard 1,100 ppm F sodium fluoride positive control dentifrice. Sodium Fluoride 175-190 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 15525462-0 2004 Homocysteine induces production of monocyte chemoattractant protein-1 and interleukin-8 in cultured human whole blood. Homocysteine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 15525462-1 2004 AIM: To investigate whether increased plasma L-homocysteine (Hcy) level could promote monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) in cultured whole blood. Homocysteine 45-59 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 15525462-1 2004 AIM: To investigate whether increased plasma L-homocysteine (Hcy) level could promote monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) in cultured whole blood. Homocysteine 45-59 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 15525462-1 2004 AIM: To investigate whether increased plasma L-homocysteine (Hcy) level could promote monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) in cultured whole blood. Homocysteine 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 15525462-1 2004 AIM: To investigate whether increased plasma L-homocysteine (Hcy) level could promote monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) in cultured whole blood. Homocysteine 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 15525462-8 2004 radicals, play extremely important role in the Hcy-induced MCP-1 and IL-8 production. Homocysteine 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 15525462-9 2004 CONCLUSION: Increased Hcy level in plasma (hyperhomocysteinemia) induced MCP-1 and IL-8 secretion in cultured human whole blood, especially in monocytes via oxidative stress mechanism. Homocysteine 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 15502050-3 2004 We investigated the hypothesis that preincisional IV pentoxifylline (PTX) treatment could attenuate the release of proinflammatory (tumor necrosis factor, interleukin (IL)-1beta, IL-6, and IL-8) and antiinflammatory (IL-1 receptor antagonist) cytokines in patients who underwent elective colorectal cancer surgery. Pentoxifylline 53-67 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 15502050-3 2004 We investigated the hypothesis that preincisional IV pentoxifylline (PTX) treatment could attenuate the release of proinflammatory (tumor necrosis factor, interleukin (IL)-1beta, IL-6, and IL-8) and antiinflammatory (IL-1 receptor antagonist) cytokines in patients who underwent elective colorectal cancer surgery. Pentoxifylline 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 15528909-1 2004 The objective of this research was to evaluate the anticaries effectiveness of a low-dose (500 ppm F, low-NaF) sodium fluoride dentifrice, a high-dose (2,800 ppm F, high-NaF) sodium fluoride dentifrice and an experimental 0.454% stabilized stannous fluoride (1,100 ppm F) with sodium hexametaphosphate (SnF2-HMP) dentifrice, each relative to a standard 1,100 ppm F sodium fluoride positive control dentifrice. Sodium Fluoride 175-190 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 15550066-5 2004 Effects of PD98059, SB202190 and SP600125 (inhibitors of ERK, p38 and JNK, respectively) on IL-1beta-induced secretion of IL-6 and IL-8, and on IL-1beta-induced expression of cyclo-oxygenase-2 (COX-2) in endometriotic cells were studied. pyrazolanthrone 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 15550066-8 2004 Both SB202190 and SP600125 suppressed IL-1beta-induced secretion of IL-6 and IL-8, and PD98059 suppressed IL-1beta-induced secretion of IL-8. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 5-13 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15550066-8 2004 Both SB202190 and SP600125 suppressed IL-1beta-induced secretion of IL-6 and IL-8, and PD98059 suppressed IL-1beta-induced secretion of IL-8. pyrazolanthrone 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15550066-8 2004 Both SB202190 and SP600125 suppressed IL-1beta-induced secretion of IL-6 and IL-8, and PD98059 suppressed IL-1beta-induced secretion of IL-8. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 87-94 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 15458513-5 2004 RESULTS: Increased interleukin 1beta (IL1beta) and IL8 release by in vitro cultured normal PBMC was observed after stimulation with LTA at concentrations > or =5 microg/mL; these levels were lower than for lipopolysaccharide (LPS)-stimulated cells and LTA antagonized LPS-induced cytokine release by normal PBMC. lipoteichoic acid 132-135 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 15544591-8 2004 There was a significant increase in CysLT(1) and BLT(1) receptor expression, as well as a release of LTB(4) and IL-8 after exposure to isocyanates compared with the baseline, only in subjects with isocyanate-induced asthma, whereas there was no increase in LTC(4). Isocyanates 135-145 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 15519527-4 2004 Treatment with the mitogen-activated protein kinase/extracellular signal-related kinase (MEK) inhibitor U0126 reduced expression of VEGF and IL-8 in MDA-MB-231 cells, partially inhibited expression in MDA-MB-468 and Hs578T cells, with minimal effects in GI101A cells. U 0126 104-109 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 15491751-2 2004 Here, we investigate a second mechanism in which LPA enhances cellular invasion through the increased expression of IL-8, independent of the expression or activation of MMP2. lysophosphatidic acid 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 15491751-0 2004 Lysophosphatidic acid enhances epithelial ovarian carcinoma invasion through the increased expression of interleukin-8. lysophosphatidic acid 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 15546258-10 2004 The increase in IL-8 was accompanied by a parallel increase in cyclic adenosine monophosphate. Cyclic AMP 63-93 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15546258-12 2004 The transient increase in the levels of IL-8 concurs with the results of recent experimental research showing a calcitonin gene-related peptide-induced activation of IL-8 gene expression, but not RANTES and MCP-1, via the transcriptional factor AP-2, which mediates transduction in response to cyclic adenosine monophosphate. Cyclic AMP 294-324 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 15546258-12 2004 The transient increase in the levels of IL-8 concurs with the results of recent experimental research showing a calcitonin gene-related peptide-induced activation of IL-8 gene expression, but not RANTES and MCP-1, via the transcriptional factor AP-2, which mediates transduction in response to cyclic adenosine monophosphate. Cyclic AMP 294-324 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 15491751-3 2004 METHODS: Epithelial ovarian carcinoma cells (DOV 13) were exposed to LPA (80 microM) and IL-8 (100 ng/ml) for 24 h. IL-8 expression was quantified by enzyme-linked immunosorbent assay (ELISA). lysophosphatidic acid 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 15491751-7 2004 RESULTS: Our results found LPA to increase IL-8 expression threefold. lysophosphatidic acid 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 15726915-15 2004 In addition, serum level of IL-8 were significantly correlated with the serum levels of HDL-cholesterol, total cholesterol and BMI in pre-eclamptic women (r= 0.368, p < 0.05; r=0.513, p < 0.01 and r= -0.41, p < 0.01, respectively). Cholesterol 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 15726915-15 2004 In addition, serum level of IL-8 were significantly correlated with the serum levels of HDL-cholesterol, total cholesterol and BMI in pre-eclamptic women (r= 0.368, p < 0.05; r=0.513, p < 0.01 and r= -0.41, p < 0.01, respectively). Cholesterol 111-122 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 15514602-10 2004 RESULTS: Suberoylanilide hydroxamic acid significantly enhanced interleukin 8 and nuclear factor kappaB-dependent reporter gene transcription, and these effects were inhibited by bortezomib ( P < or = .01). Vorinostat 9-40 C-X-C motif chemokine ligand 8 Homo sapiens 64-122 15485475-9 2004 Circulating MCP-1 and IL-8 levels rose after the methionine load (P < 0.001), but not after placebo or methionine plus vitamins. Methionine 49-59 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 15501764-10 2004 In this regard, the ability of LT-IIbB to activate NF-kappaB and induce TNF-alpha and IL-8 was antagonized by the LT-IIb holotoxin. stichoposide 121-130 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 15334663-0 2004 Characterization of the biological activities of uridine diphosphate in human dendritic cells: Influence on chemotaxis and CXCL8 release. Uridine Diphosphate 49-68 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 15334663-8 2004 Instead, UDP, but not UTP, stimulated the release of the CXC-chemokine 8 (CXCL8) from mature DC in a reactive blue sensitive manner. Uridine Diphosphate 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 74-79 15334663-9 2004 Moreover, our study indicates that UDP stimulates different signaling pathways in immature and mature DC in order to favor the accumulation of immature DC and to augment the capacity to secrete CXCL8 in mature DC. Uridine Diphosphate 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 194-199 15622447-0 2004 Hyperforin, the active component of St. John"s wort, induces IL-8 expression in human intestinal epithelial cells via a MAPK-dependent, NF-kappaB-independent pathway. hyperforin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15622447-2 2004 Although St. John"s wort has been reported to have minimal side effects compared with other antidepressants, here we show that hyperforin, the active component of St. John"s wort, can stimulate interleukin-8 (IL-8) expression in human intestinal epithelia cells (IEC) and primary hepatocytes. hyperforin 127-137 C-X-C motif chemokine ligand 8 Homo sapiens 194-207 15622447-2 2004 Although St. John"s wort has been reported to have minimal side effects compared with other antidepressants, here we show that hyperforin, the active component of St. John"s wort, can stimulate interleukin-8 (IL-8) expression in human intestinal epithelia cells (IEC) and primary hepatocytes. hyperforin 127-137 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 15622447-5 2004 Although hyperforin is a potent ligand for the steroid and xenobiotic receptor (SXR), we found that hyperforin induced IL-8 mRNA through an SXR-independent transcriptional activation pathway. hyperforin 100-110 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 15514602-10 2004 RESULTS: Suberoylanilide hydroxamic acid significantly enhanced interleukin 8 and nuclear factor kappaB-dependent reporter gene transcription, and these effects were inhibited by bortezomib ( P < or = .01). Bortezomib 179-189 C-X-C motif chemokine ligand 8 Homo sapiens 64-122 15507849-5 2004 RESULTS: Urinary IL-6 and IL-8 levels [IL-6, IL-8/creatinine (pg/mg)] were significantly higher in group I than in group II (Il-6 level: 39.4+/-41.1 vs. 6.3+/-13.7, p<0.01; IL-8 level: 791.1+/-1143.6 vs. 36+/-87.9, p<0.001). Creatinine 50-60 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 15247267-7 2004 Furthermore, inhibition of the EGF receptor by AG1478 significantly reduced NT-induced IL-8 promoter activity and IL-8 secretion. RTKI cpd 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 15622447-6 2004 IL-8 induction by hyperforin required the activation of AP-1 but not the NF-kappaB transcription factor, thereby distinguishing it from the NF-kappaB-dependent IL-8 induction mediated by tumor necrosis factor alpha (TNFalpha). hyperforin 18-28 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15622447-7 2004 Further study revealed that extracellular signal-regulated kinase 1 and 2 (ERK1/2) were required for the hyperforin-induced expression of IL-8. hyperforin 105-115 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 15369845-4 2004 In addition, production of IL-8 in the U937 cell line increased up to eight-fold at levels of DON just lower than the most toxic one, suggesting that IL-8 can be used as an additional index for cytotoxicity in mononuclear phagocytes. deoxynivalenol 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15369845-4 2004 In addition, production of IL-8 in the U937 cell line increased up to eight-fold at levels of DON just lower than the most toxic one, suggesting that IL-8 can be used as an additional index for cytotoxicity in mononuclear phagocytes. deoxynivalenol 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 15627874-8 2004 However, there was a significantly positive correlation between BALF IL-8 and nitrite levels in patients with CF (r = 0.5) and also in control patients (r = 0.6). Nitrites 78-85 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 15464826-4 2004 Furthermore, it is not known if the previously demonstrated effects on basal and dust-induced IL-6 and IL-8 protein production by 8-bromo-cyclicAMP are time-dependent, since only cumulative effects are observed by measurement of cytokine release. 8-Bromo Cyclic Adenosine Monophosphate 130-147 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 15464826-8 2004 At 1-1.5 h, 8-bromo-cAMP stimulated basal and dust-induced IL-6 mRNA expression and attenuated dust-induced IL-8 mRNA expression by activation of protein kinase A- (PKA), as assessed with the PKA inhibitor H-89. 8-Bromo Cyclic Adenosine Monophosphate 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 15464826-9 2004 On prolonged exposure (>3 h), the dust-induced IL-6 mRNA was PKA-dependently decreased, whereas at 17 h and longer the IL-8 mRNA expression induced by a dust-suspension with 8-bromo-cAMP was similar to, or enhanced, relative to the dust-induced IL-8 mRNA. 8-Bromo Cyclic Adenosine Monophosphate 177-189 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15464826-10 2004 Thus, 8-bromo-cAMP exerted opposite action on dust-induced IL-6 and IL-8 mRNA expression with time. 8-Bromo Cyclic Adenosine Monophosphate 6-18 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 15388640-1 2004 Oxidized phospholipids, including oxidation products of palmitoyl-arachidonyl-phosphatidyl choline (PAPC), are mediators of inflammation in endothelial cells (ECs) and known to induce several chemokines, including interleukin-8 (IL-8). Phospholipids 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 214-227 15247267-7 2004 Furthermore, inhibition of the EGF receptor by AG1478 significantly reduced NT-induced IL-8 promoter activity and IL-8 secretion. RTKI cpd 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 15388640-1 2004 Oxidized phospholipids, including oxidation products of palmitoyl-arachidonyl-phosphatidyl choline (PAPC), are mediators of inflammation in endothelial cells (ECs) and known to induce several chemokines, including interleukin-8 (IL-8). Phospholipids 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 229-233 15388640-7 2004 Furthermore, cholesterol loading of ECs by either the cholesterol-cyclodextrin complex or caveolin-1 overexpression inhibited OxPAPC induction of IL-8. Cholesterol 54-65 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 15388640-7 2004 Furthermore, cholesterol loading of ECs by either the cholesterol-cyclodextrin complex or caveolin-1 overexpression inhibited OxPAPC induction of IL-8. Cyclodextrins 66-78 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 15388640-8 2004 These observations suggest that changes in cholesterol level can modulate IL-8 synthesis in ECs. Cholesterol 43-54 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15388640-1 2004 Oxidized phospholipids, including oxidation products of palmitoyl-arachidonyl-phosphatidyl choline (PAPC), are mediators of inflammation in endothelial cells (ECs) and known to induce several chemokines, including interleukin-8 (IL-8). palmitoyl-arachidonyl-phosphatidyl choline 56-98 C-X-C motif chemokine ligand 8 Homo sapiens 214-227 15388640-1 2004 Oxidized phospholipids, including oxidation products of palmitoyl-arachidonyl-phosphatidyl choline (PAPC), are mediators of inflammation in endothelial cells (ECs) and known to induce several chemokines, including interleukin-8 (IL-8). palmitoyl-arachidonyl-phosphatidyl choline 56-98 C-X-C motif chemokine ligand 8 Homo sapiens 229-233 15388640-1 2004 Oxidized phospholipids, including oxidation products of palmitoyl-arachidonyl-phosphatidyl choline (PAPC), are mediators of inflammation in endothelial cells (ECs) and known to induce several chemokines, including interleukin-8 (IL-8). PAPC 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 214-227 15388640-1 2004 Oxidized phospholipids, including oxidation products of palmitoyl-arachidonyl-phosphatidyl choline (PAPC), are mediators of inflammation in endothelial cells (ECs) and known to induce several chemokines, including interleukin-8 (IL-8). PAPC 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 229-233 15388640-5 2004 We also provide evidence that cholesterol depletion and SREBP activation are signals for OxPAPC induction of IL-8. Cholesterol 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 15388640-6 2004 Cholesterol depletion by methyl-beta-cyclodextrin induced IL-8 synthesis in a dose-dependent manner. Cholesterol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 15388640-6 2004 Cholesterol depletion by methyl-beta-cyclodextrin induced IL-8 synthesis in a dose-dependent manner. methyl-beta-cyclodextrin 25-49 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 15388640-10 2004 Overexpression of either dominant-negative SREBP cleavage-activating protein or 25-hydroxycholesterol significantly suppressed the effect of OxPAPC on IL-8 transcription. Hydroxycholesterols 83-101 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 15354211-10 2004 However, the magnitude of IL-8 secretion induced by cytochalasin cannot be accounted for by integrin signalling and may reflect the influence of another signalling pathway or a novel, intrinsic cytoskeletal function. Cytochalasins 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 15586939-0 2004 Stimulation of endothelial IL-8 (eIL-8) production and apoptosis by phenolic metabolites of benzene in HL-60 cells and human bone marrow endothelial cells. Benzene 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15586939-2 2004 One potential mechanism of apoptosis induced by benzene metabolites that has not been examined is the production of pro-apoptotic cytokines such as endothelial IL-8 from endothelial cells in bone marrow stroma. Benzene 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 15388640-7 2004 Furthermore, cholesterol loading of ECs by either the cholesterol-cyclodextrin complex or caveolin-1 overexpression inhibited OxPAPC induction of IL-8. Cholesterol 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 15483420-3 2004 We determined the effects of theaflavin, a black tea-derived polyphenol, on tumor necrosis factor-alpha-mediated expression of the interleukin-8 gene in A549 cells. theaflavin 29-39 C-X-C motif chemokine ligand 8 Homo sapiens 131-144 15180920-4 2004 Resveratrol and the related molecule quercetin, but not deoxyrhapontin, inhibited IL-8 and granulocyte-macrophage colony-stimulating factor release from A549 cells. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 82-147 15180920-4 2004 Resveratrol and the related molecule quercetin, but not deoxyrhapontin, inhibited IL-8 and granulocyte-macrophage colony-stimulating factor release from A549 cells. Quercetin 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 82-147 15308550-9 2004 Exogenous ADMA also stimulated secretion of MCP-1 and interleukin-8. N,N-dimethylarginine 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 15344968-9 2004 In the LTX group, total cell counts, neutrophil percentages and IL-8 levels were much higher in SI than BAL (1.6 x 10(6)/mL, 65.5% and 54.2 ng/mL vs. 0.1 x 10(6)/mL, 3.0% and 0.01 ng/mL; p < 0.001). Leukotriene C4 7-10 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 15169673-0 2004 Nitric oxide increases IL-8 gene transcription and mRNA stability to enhance IL-8 gene expression in lung epithelial cells. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 15169673-0 2004 Nitric oxide increases IL-8 gene transcription and mRNA stability to enhance IL-8 gene expression in lung epithelial cells. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15169673-3 2004 The association between elevated levels of nitric oxide (NO) and IL-8 in acute lung injury associated with sepsis, acute respiratory distress syndrome, respiratory syncytial virus infection in infants, and other inflammatory diseases suggested that NO may play important roles in the control of IL-8 gene expression in the lung. Nitric Oxide 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 15169673-3 2004 The association between elevated levels of nitric oxide (NO) and IL-8 in acute lung injury associated with sepsis, acute respiratory distress syndrome, respiratory syncytial virus infection in infants, and other inflammatory diseases suggested that NO may play important roles in the control of IL-8 gene expression in the lung. Nitric Oxide 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 295-299 15169673-9 2004 NO induction of IL-8 mRNA was significantly reduced by inhibitors of extracellular regulated kinase and protein kinase C. IL-8 induction by NO was also reduced by hydroxyl radical scavengers such as dimethyl sulfoxide and dimethylthiourea, indicating the involvement of hydroxyl radicals in the induction process. Hydroxyl Radical 163-179 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15169673-9 2004 NO induction of IL-8 mRNA was significantly reduced by inhibitors of extracellular regulated kinase and protein kinase C. IL-8 induction by NO was also reduced by hydroxyl radical scavengers such as dimethyl sulfoxide and dimethylthiourea, indicating the involvement of hydroxyl radicals in the induction process. Hydroxyl Radical 163-179 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15169673-9 2004 NO induction of IL-8 mRNA was significantly reduced by inhibitors of extracellular regulated kinase and protein kinase C. IL-8 induction by NO was also reduced by hydroxyl radical scavengers such as dimethyl sulfoxide and dimethylthiourea, indicating the involvement of hydroxyl radicals in the induction process. Dimethyl Sulfoxide 199-217 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15169673-9 2004 NO induction of IL-8 mRNA was significantly reduced by inhibitors of extracellular regulated kinase and protein kinase C. IL-8 induction by NO was also reduced by hydroxyl radical scavengers such as dimethyl sulfoxide and dimethylthiourea, indicating the involvement of hydroxyl radicals in the induction process. Dimethyl Sulfoxide 199-217 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15169673-9 2004 NO induction of IL-8 mRNA was significantly reduced by inhibitors of extracellular regulated kinase and protein kinase C. IL-8 induction by NO was also reduced by hydroxyl radical scavengers such as dimethyl sulfoxide and dimethylthiourea, indicating the involvement of hydroxyl radicals in the induction process. 1,3-dimethylthiourea 222-238 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15169673-9 2004 NO induction of IL-8 mRNA was significantly reduced by inhibitors of extracellular regulated kinase and protein kinase C. IL-8 induction by NO was also reduced by hydroxyl radical scavengers such as dimethyl sulfoxide and dimethylthiourea, indicating the involvement of hydroxyl radicals in the induction process. 1,3-dimethylthiourea 222-238 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15169673-9 2004 NO induction of IL-8 mRNA was significantly reduced by inhibitors of extracellular regulated kinase and protein kinase C. IL-8 induction by NO was also reduced by hydroxyl radical scavengers such as dimethyl sulfoxide and dimethylthiourea, indicating the involvement of hydroxyl radicals in the induction process. Hydroxyl Radical 270-287 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15169673-9 2004 NO induction of IL-8 mRNA was significantly reduced by inhibitors of extracellular regulated kinase and protein kinase C. IL-8 induction by NO was also reduced by hydroxyl radical scavengers such as dimethyl sulfoxide and dimethylthiourea, indicating the involvement of hydroxyl radicals in the induction process. Hydroxyl Radical 270-287 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15476228-15 2004 Methotrexate reduced synovial IL-1alpha, IL-1beta, IL-8, IL-10, IL-15, IFNgamma, and TNFalpha mRNA expression, but the effect was significant only for IL-8. Methotrexate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 15476228-15 2004 Methotrexate reduced synovial IL-1alpha, IL-1beta, IL-8, IL-10, IL-15, IFNgamma, and TNFalpha mRNA expression, but the effect was significant only for IL-8. Methotrexate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 15476228-16 2004 CONCLUSION: Methotrexate produced a clinical response in PsA by reducing, but not abolishing, the inflammatory infiltrate, adhesion molecule expression, and MMP-3 and proinflammatory cytokine gene expression, particularly IL-8, in the synovium. Methotrexate 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 15380914-6 2004 RESULTS: Allicin markedly inhibited the spontaneous and TNF-alpha -induced secretion of IL-1beta, IL-8, IP-10 and MIG from the two different cell lines in a dose-dependent manner and suppressed the expression of IL-8 and IL-1beta mRNA levels. allicin 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 15380914-6 2004 RESULTS: Allicin markedly inhibited the spontaneous and TNF-alpha -induced secretion of IL-1beta, IL-8, IP-10 and MIG from the two different cell lines in a dose-dependent manner and suppressed the expression of IL-8 and IL-1beta mRNA levels. allicin 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 212-216 15302455-6 2004 The discs were subjected to 1 min exposures of 0.2% sodium fluoride (NaF); the F re-release was assessed for another 12 h. RESULTS: Following a brief initial burst of F release, the rate decreased rapidly. Sodium Fluoride 52-67 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 15302455-12 2004 After sodium fluoride (NaF) treatment, F can be recharged easily and re-released rapidly within 90 min. Sodium Fluoride 6-21 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 15483420-8 2004 MEASUREMENTS AND MAIN RESULTS: Theaflavin inhibited tumor necrosis factor-alpha-mediated interleukin-8 gene expression, as measured by luciferase assay and Northern blot analysis, at concentrations of 10 and 30 microg/mL. theaflavin 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 15483420-9 2004 This effect appears to primarily involve inhibition of interleukin-8 transcription because theaflavin inhibited tumor necrosis factor-alpha-mediated activation of the interleukin-8 promoter in cells transiently transfected with an interleukin-8 promoter-luciferase reporter plasmid. theaflavin 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 15483420-9 2004 This effect appears to primarily involve inhibition of interleukin-8 transcription because theaflavin inhibited tumor necrosis factor-alpha-mediated activation of the interleukin-8 promoter in cells transiently transfected with an interleukin-8 promoter-luciferase reporter plasmid. theaflavin 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 15483420-9 2004 This effect appears to primarily involve inhibition of interleukin-8 transcription because theaflavin inhibited tumor necrosis factor-alpha-mediated activation of the interleukin-8 promoter in cells transiently transfected with an interleukin-8 promoter-luciferase reporter plasmid. theaflavin 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 15483420-12 2004 CONCLUSIONS: We conclude that theaflavin is a potent inhibitor of interleukin-8 gene expression in vitro. theaflavin 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 15474071-9 2004 Production of both IL-8 and M-CSF was statistically significantly increased by IL-1alpha plus C6-ceramide as compared with IL-1alpha alone; however, IL-6 production was not increased. N-caproylsphingosine 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 15364099-9 2004 ASBG affected the production of IL-8 by human peripheral blood mononuclear cells (PBMC). asbg 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 15474070-6 2004 MAIN OUTCOME MEASURE(S): We determined the effect of LPS on the production of TNFalpha and IL-8 and the effect of IL-8 antisense oligonucleotide and nuclear factor-kappaB (NF-kappaB) inhibitor on IL-8 production using ELISA. Oligonucleotides 129-144 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 15474070-6 2004 MAIN OUTCOME MEASURE(S): We determined the effect of LPS on the production of TNFalpha and IL-8 and the effect of IL-8 antisense oligonucleotide and nuclear factor-kappaB (NF-kappaB) inhibitor on IL-8 production using ELISA. Oligonucleotides 129-144 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 15474070-12 2004 IL-8 antisense oligonucleotide and NF-kappaB inhibitor significantly decreased LPS-induced IL-8 protein production and LPS-induced ESC proliferation. Oligonucleotides 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15474071-10 2004 CONCLUSION(S): The results suggest that IL-1alpha stimulates the production of IL-8 and M-CSF by a mechanism that involves the sphingomyelin-ceramide system. Sphingomyelins 127-140 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 15474070-12 2004 IL-8 antisense oligonucleotide and NF-kappaB inhibitor significantly decreased LPS-induced IL-8 protein production and LPS-induced ESC proliferation. Oligonucleotides 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 15474071-0 2004 Synergistic effect of interleukin (IL)-1alpha and ceramide analogue on the production of IL-6, IL-8, and macrophage colony-stimulating factor by endometrial stromal cells. Ceramides 50-58 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 15474071-10 2004 CONCLUSION(S): The results suggest that IL-1alpha stimulates the production of IL-8 and M-CSF by a mechanism that involves the sphingomyelin-ceramide system. Ceramides 141-149 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 15474071-2 2004 DESIGN: The effects of IL-1alpha, IL-1 receptor antagonist (IL-1RA), C2-ceramide, and C6-ceramide on the production of IL-6, IL-8, and M-CSF by ESC. N-acetylsphingosine 69-80 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 15474071-11 2004 Ceramide may be important in increasing the production of IL-8 and M-CSF in the human endometrium. Ceramides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 16134003-5 2004 GD (0.01-1 mg/mL)-containing medium in stimulated culture supernatants dose-dependently and significantly decreased IL-8, IL-13, and tumor necrosis factor-alpha secretion on the phorbol 12-myristate 13-acetate and A23187-stimulated HMC-1. Gadolinium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 15385484-10 2004 Induction of IL-8 mRNA expression occurs rapidly and ceases by 6 h after BFT treatment, whereas IL-8 secretion continues to increase for at least 18 h. Our data suggest that BFT-stimulated IL-8 secretion involves tyrosine kinase-dependent activation of nuclear factor-kappaB (NF-kappaB) as well as activation of the mitogen-activated protein kinases (MAPKs), p38 and extracellular signal-related kinase. SCHEMBL13664687 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 15385484-10 2004 Induction of IL-8 mRNA expression occurs rapidly and ceases by 6 h after BFT treatment, whereas IL-8 secretion continues to increase for at least 18 h. Our data suggest that BFT-stimulated IL-8 secretion involves tyrosine kinase-dependent activation of nuclear factor-kappaB (NF-kappaB) as well as activation of the mitogen-activated protein kinases (MAPKs), p38 and extracellular signal-related kinase. SCHEMBL13664687 174-177 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 15385484-10 2004 Induction of IL-8 mRNA expression occurs rapidly and ceases by 6 h after BFT treatment, whereas IL-8 secretion continues to increase for at least 18 h. Our data suggest that BFT-stimulated IL-8 secretion involves tyrosine kinase-dependent activation of nuclear factor-kappaB (NF-kappaB) as well as activation of the mitogen-activated protein kinases (MAPKs), p38 and extracellular signal-related kinase. SCHEMBL13664687 174-177 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 15385484-10 2004 Induction of IL-8 mRNA expression occurs rapidly and ceases by 6 h after BFT treatment, whereas IL-8 secretion continues to increase for at least 18 h. Our data suggest that BFT-stimulated IL-8 secretion involves tyrosine kinase-dependent activation of nuclear factor-kappaB (NF-kappaB) as well as activation of the mitogen-activated protein kinases (MAPKs), p38 and extracellular signal-related kinase. SCHEMBL13664687 174-177 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 15385484-11 2004 Simultaneous activation of NF-kappaB and MAPKs appears necessary for secretion of IL-8 by HT29/C1 cells treated with BFT. SCHEMBL13664687 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 15326096-6 2004 Pg-LP, as well as Ec-LPS, was potent in inducing IL-8 production in human gingival fibroblasts. pg-lp 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 15326096-6 2004 Pg-LP, as well as Ec-LPS, was potent in inducing IL-8 production in human gingival fibroblasts. ec-lps 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 15219635-6 2004 In analyses adjusting for age, body mass index (BMI), fasting cholesterol, alcohol use, race and 17beta-estradiol (E(2)), higher Ho scores were associated with greater LPS-stimulated expression of IL-1alpha (beta = 0.033, p = 0.02), IL-8 (beta = 0.046, p = 0.01) and IL-1beta (beta = 0.024, p = 0.06). Estradiol 97-113 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 15377293-5 2004 Although gadolinium chloride treatment did not affect the level of serum TNF-alpha, it significantly reduced that of interleukin (IL)-8 and neutrophil migration in the hepatic sinusoids after the lipopolysaccharide challenge. gadolinium chloride 9-28 C-X-C motif chemokine ligand 8 Homo sapiens 117-135 15269287-0 2004 Sulfasalazine down-regulates the expression of the angiogenic factors platelet-derived endothelial cell growth factor/thymidine phosphorylase and interleukin-8 in human monocytic-macrophage THP1 and U937 cells. Sulfasalazine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 146-159 15269287-2 2004 Here, we show that prolonged exposure of human monocytic/macrophage THP1 and U937 cells to sulfasalazine, an anti-inflammatory drug and inhibitor of nuclear factor-kappaB (NF-kappaB), resulted in down-regulation of PD-ECGF/TP and IL-8 (mRNA, protein and activity) along with elimination of their induction by tumor necrosis factor-alpha and interferon-gamma. Sulfasalazine 91-104 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 15494123-5 2004 IkappaBalphaM inhibited in vitro and in vivo expression of vascular endothelial growth factor (VEGF) and interleukin 8 (IL-8). ikappabalpham 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 15494123-5 2004 IkappaBalphaM inhibited in vitro and in vivo expression of vascular endothelial growth factor (VEGF) and interleukin 8 (IL-8). ikappabalpham 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 15626158-2 2004 Thioglycollate-elicited neutrophils from BALB/c mice failed to respond to vCXCL-1 while retaining the capacity to respond to known murine (Mu) CXCR2 ligands, such as hCXCL8 (IL8) and mCXCL1 (KC). Thioglycolates 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 166-172 15514524-5 2004 We hypothesize that pRBC transfusion induces increased IL-8 gene expression that is avoided by the use of PolyHb. polyhb 106-112 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 15514524-10 2004 PolyHb IL-8 mRNA was less than pRBC transfused (p <0.01). polyhb 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 15514524-11 2004 In PMNs, simulated transfusion of pRBCs increase IL-8 mRNA (RB=3.17 +/- 1.05 amol/microg total RNA, RB + pRBC=7.60 +/- 1.79 amol/microg total RNA, p <0.01), whereas PolyHb did not (RB + PolyHb=4.53 +/- 1.64 amol/microg total RNA). Rubidium 35-37 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 15240896-3 2004 Our results show that silica particles induced a concentration- and time-dependent increase in interleukin (IL)-8 release from the human epithelial lung cell line A549. Silicon Dioxide 22-28 C-X-C motif chemokine ligand 8 Homo sapiens 95-113 15453805-10 2004 We noted a significant elevation of il-8 in men with bone metastases, diagnosed by Tc-99 MDP bone scan, when compared to men with localized disease (Figure 1). tc-99 mdp 83-92 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 15251176-9 2004 When cells exposed to 200 microM SM were treated with the p38 MAP kinase inhibitor SB203580, the levels of IL-8, IL-6, and TNF-alpha and IL-1beta were significantly decreased when compared with cells that were untreated. Samarium 33-35 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 15240896-4 2004 The IL-8 induction was significantly attenuated by inhibitors of the mitogen-activated protein kinases (MAPKs), p38 (SB202190) and extracellular signal-regulated kinase (ERK)-1 and -2 (PD98059), as well as a general protein tyrosine kinase (PTK) inhibitor (genistein). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 185-192 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 15251176-9 2004 When cells exposed to 200 microM SM were treated with the p38 MAP kinase inhibitor SB203580, the levels of IL-8, IL-6, and TNF-alpha and IL-1beta were significantly decreased when compared with cells that were untreated. SB 203580 83-91 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 15240896-4 2004 The IL-8 induction was significantly attenuated by inhibitors of the mitogen-activated protein kinases (MAPKs), p38 (SB202190) and extracellular signal-regulated kinase (ERK)-1 and -2 (PD98059), as well as a general protein tyrosine kinase (PTK) inhibitor (genistein). Genistein 257-266 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 15240896-5 2004 However, IL-8 induction was most efficiently inhibited by the Src family kinase (SFK) inhibitor, PP2, suggesting a crucial role of SFKs in regulating silica-induced IL-8 release from A549 cells. Silicon Dioxide 150-156 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 15240896-5 2004 However, IL-8 induction was most efficiently inhibited by the Src family kinase (SFK) inhibitor, PP2, suggesting a crucial role of SFKs in regulating silica-induced IL-8 release from A549 cells. Silicon Dioxide 150-156 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 15240896-9 2004 Our results suggest the presence of two separate signaling pathways which are important in the regulation of silica-induced IL-8 release from A549 cells; one involving SFK-dependent activation of ERK1/2, and the other activation of p38, at least partly independent of SFKs. Silicon Dioxide 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 15251176-2 2004 Previous work has revealed that SM induces the production of inflammatory cytokines, including IL-8, IL-6, TNF-alpha, and IL-1beta, in keratinocytes. Samarium 32-34 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 15286717-0 2004 Inhibitory effects of cyclosporin A on calcium mobilization-dependent interleukin-8 expression and invasive potential of human glioblastoma U251MG cells. Calcium 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 15562785-4 2004 RESULTS: IL-8 and TNF-alpha levels in EPS were higher in men with CBP [(10967.5 +/- 3477.7) pg/ml, (84.1 +/- 54.7) pg/ml] or CPPS IIIA [(9268.4 +/- 2034.6) pg/ml and (32.6 +/- 18.6) pg/ml], but lower in men with CPPS IIIB [(2726.1 +/- 277.5) pg/ml, (12.6 +/- 7.1) pg/ml] or controls [(2800.0 +/- 320.2) pg/ml and (12.9 +/- 10.1) pg/ml] respectively. exophthalmos producing substance 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 15280372-6 2004 Treatment of HBEpCs with LPA increased both IL-8 gene and protein expression, which was coupled to Gi and G(12/13) proteins. lysophosphatidic acid 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 15280372-8 2004 Furthermore, LPA-activated PKCdelta and the LPA-mediated activation of NF-kappaB and IL-8 production were attenuated by overexpression of dominant-negative PKCdelta and rottlerin. lysophosphatidic acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 15280372-8 2004 Furthermore, LPA-activated PKCdelta and the LPA-mediated activation of NF-kappaB and IL-8 production were attenuated by overexpression of dominant-negative PKCdelta and rottlerin. rottlerin 169-178 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 15280372-10 2004 These results demonstrate for the first time that LPA is a potent stimulator of IL-8 production in HBEpCs, which involves PKCdelta/NF-kappaB signaling pathways. lysophosphatidic acid 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 15364009-4 2004 Benidipine also suppressed induction of monocyte chemoattractant protein (MCP)-1 and interleukin-8. benidipine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 85-98 15286717-3 2004 Combined treatment with Ca(2+)-ionophore and phorbol-myristate-acetate (A23187/PMA) increased IL-8 mRNA and protein levels. Tetradecanoylphorbol Acetate 45-70 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 15286717-3 2004 Combined treatment with Ca(2+)-ionophore and phorbol-myristate-acetate (A23187/PMA) increased IL-8 mRNA and protein levels. Calcimycin 72-78 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 15358661-5 2004 Treatment of T24 and 5637 cells with phosphatidylinositol-specific phospholipase C to eliminate CD14 from the cell surface dramatically suppressed the induction of IL-8. Phosphatidylinositols 37-57 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 15337792-6 2004 Theophylline induced a sixfold increase in HDAC activity in COPD AM lysates and significantly enhanced dexamethasone suppression of induced IL-8 release, an effect that was blocked by the HDAC inhibitor trichostatin A. Theophylline 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 15337792-6 2004 Theophylline induced a sixfold increase in HDAC activity in COPD AM lysates and significantly enhanced dexamethasone suppression of induced IL-8 release, an effect that was blocked by the HDAC inhibitor trichostatin A. Dexamethasone 103-116 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 15337792-6 2004 Theophylline induced a sixfold increase in HDAC activity in COPD AM lysates and significantly enhanced dexamethasone suppression of induced IL-8 release, an effect that was blocked by the HDAC inhibitor trichostatin A. trichostatin A 203-217 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 15517885-4 2004 Resveratrol has been shown to suppress the activation of several transcription factors, including NF-kappaB, AP-1 and Egr-1; to inhibit protein kinases including IkappaBalpha kinase, JNK, MAPK, Akt, PKC, PKD and casein kinase II; and to down-regulate products of genes such as COX-2, 5-LOX, VEGF, IL-1, IL-6, IL-8, AR and PSA. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 309-313 15302676-7 2004 Repertaxin also prevented CXCL8-induced calcium influx but not CXCL8 binding to purified rat neutrophils. Calcium 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 15383152-7 2004 However, IL-6, IL-8, and IL-13 production induced by IL-1 beta were significantly enhanced by addition of epinephrine. Epinephrine 106-117 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 15117678-6 2004 Expression of IL-1beta, IL-6, IL-8, and COX-2 mRNA was reduced by 30 microM PP1, an Src family tyrosine kinase inhibitor, and by 25 microM SB-203580, a p38 MAPK inhibitor. SB 203580 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 15252191-3 2004 OBJECTIVE: To evaluate the antiinflammatory effect of clarithromycin on serum and sputum interleukin-8 (IL-8), tumor necrosis factor-alpha (TNF-alpha), and leukotriene B4 levels in patients with COPD. Clarithromycin 54-68 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 15252191-3 2004 OBJECTIVE: To evaluate the antiinflammatory effect of clarithromycin on serum and sputum interleukin-8 (IL-8), tumor necrosis factor-alpha (TNF-alpha), and leukotriene B4 levels in patients with COPD. Clarithromycin 54-68 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 15252191-9 2004 After the treatment, the induced sputum total cell counts, and IL-8 and TNF-alpha levels decreased significantly in the clarithromycin group compared with pretreatment levels (mean +/- SD IL-8 1606 +/- 367.3 vs 882 +/- 143.6 pg/mL, p = 0.001; TNF-alpha 638.2 +/- 287.5 vs 390 +/- 235 pg/mL, p = 0.001). Clarithromycin 120-134 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 15252191-9 2004 After the treatment, the induced sputum total cell counts, and IL-8 and TNF-alpha levels decreased significantly in the clarithromycin group compared with pretreatment levels (mean +/- SD IL-8 1606 +/- 367.3 vs 882 +/- 143.6 pg/mL, p = 0.001; TNF-alpha 638.2 +/- 287.5 vs 390 +/- 235 pg/mL, p = 0.001). Clarithromycin 120-134 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 15252191-11 2004 CONCLUSIONS: This study demonstrated that the decrease in IL-8 and TNF-alpha levels might be related to the antiinflammatory effect of clarithromycin. Clarithromycin 135-149 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 15313144-8 2004 IL-8 secretion was not altered by bradykinin or adenosine, but amiloride significantly decreased IL-8 secretion. Amiloride 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 15178703-6 2004 Moreover, an inhibitory effect of cyclosporin A, an immunosuppressor that inhibits calcineurin activity, on IL-8 release and IL-8 mRNA expression was observed. Cyclosporine 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 15352171-2 2004 Therefore, the aim of our study was to investigate, in primary cultures of human bronchial epithelial cells (HBEC), the signal transduction pathways activated by increasing concentrations (0.25, 0.5, and 1 mM) of hydrogen peroxide (H(2)O(2)), as well as their effects on IL-8 production and cell viability. Hydrogen Peroxide 213-230 C-X-C motif chemokine ligand 8 Homo sapiens 271-275 15352171-3 2004 The reported results show that H(2)O(2) elicited, in a concentration-dependent fashion, a remarkable increase in phosphorylation-dependent activation of mitogen-activated protein kinases (MAPKs), associated with a significant induction of IL-8 synthesis and a dramatically enhanced cell death. Hydrogen Peroxide 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 15352171-4 2004 Pre-treatment of HBEC with MAPK inhibitors was able to significantly inhibit the effects of H(2)O(2) on IL-8 secretion, and to effectively prevent cell death. Hydrogen Peroxide 92-100 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 15381247-0 2004 Antisense phosphorothioate oligonucleotides to NF-kappaB (RelA/NF-kappaB1) decrease interleukin-8 secretion from cultured normal human epidermal keratinocytes. Phosphorothioate Oligonucleotides 10-43 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 15178703-6 2004 Moreover, an inhibitory effect of cyclosporin A, an immunosuppressor that inhibits calcineurin activity, on IL-8 release and IL-8 mRNA expression was observed. Cyclosporine 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 15178703-7 2004 This is the first evidence of the involvement of ROS and calcium/calcineurin in IgE-dependent IL-8 production. Reactive Oxygen Species 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 15178703-7 2004 This is the first evidence of the involvement of ROS and calcium/calcineurin in IgE-dependent IL-8 production. Calcium 57-64 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 15381831-5 2004 Among the gangliosides, O-Ac-GD3, GT(1b), GD(1a), GD(1b), GT(1a), and GD3 had potent dose dependent inhibitory effects on adhesion of H. pylori to MKN-45 cells, interleukin-8 production, and vacuole formation induced by H. pylori toxin binding to Vero cells. o-ac 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 15208668-0 2004 Interleukin-1beta stimulates IL-8 expression through MAP kinase and ROS signaling in human gastric carcinoma cells. Reactive Oxygen Species 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 15252057-8 2004 Based on our results, we propose that IL-8 dimerization functions as a negative regulator for the receptor function and as a positive regulator for binding to glycosaminoglycans and that both play a role in the neutrophil recruitment process. Glycosaminoglycans 159-177 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 15362934-0 2004 Influence of eicosapentaenoic acid, an omega-3 fatty acid, on ultraviolet-B generation of prostaglandin-E2 and proinflammatory cytokines interleukin-1 beta, tumor necrosis factor-alpha, interleukin-6 and interleukin-8 in human skin in vivo. Eicosapentaenoic Acid 13-34 C-X-C motif chemokine ligand 8 Homo sapiens 204-217 15513378-12 2004 Administration of lansoprazole, a proton-pump inhibitor, decreased both IL-8 mRNA and protein levels in the esophageal mucosa. Lansoprazole 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 15208668-5 2004 Specific inhibitors of MEK-1 (PD980590) and P38 MAPK (SB203580) were found to suppress the IL-8 expression and the IL-8 promoter activity. SB 203580 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 15208668-5 2004 Specific inhibitors of MEK-1 (PD980590) and P38 MAPK (SB203580) were found to suppress the IL-8 expression and the IL-8 promoter activity. SB 203580 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15208668-5 2004 Specific inhibitors of MEK-1 (PD980590) and P38 MAPK (SB203580) were found to suppress the IL-8 expression and the IL-8 promoter activity. pd980590 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 15208668-8 2004 N-acetyl cysteine (NAC) prevented the IL-1beta-induced ROS production and IL-8 expression. Acetylcysteine 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15208668-8 2004 N-acetyl cysteine (NAC) prevented the IL-1beta-induced ROS production and IL-8 expression. Acetylcysteine 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15208668-9 2004 In addition, exogenous H2O2 could induce the IL-8 expression. Hydrogen Peroxide 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 15208668-5 2004 Specific inhibitors of MEK-1 (PD980590) and P38 MAPK (SB203580) were found to suppress the IL-8 expression and the IL-8 promoter activity. pd980590 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15208668-14 2004 The above results suggest that MAPK-AP-1 and ROS-NF-kappaB signaling pathways are involved in the IL-1beta-induced IL-8 expression and that these paracrine signaling pathways induce endothelial cell proliferation. Reactive Oxygen Species 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15311945-3 2004 We have observed that pretreatment of cells with PTIO boosted expression of IL-8 and heme oxygenase 1 (HOX) genes to a high level in cells treated with the NO donor DPTA-NO. dpta-no 165-172 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 15311945-5 2004 The effect of PTIO was abrogated by reduced glutathione, suggesting that upregulation of the IL-8 and HOX genes is dependent on RNI-mediated S-nitrosation of specific regulator(s). Glutathione 44-55 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 15311945-6 2004 The concentration of PTIO required to enhance mRNA level was different for IL-8 and HOX genes. 2-phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 15311945-7 2004 Analysis of 4,5-diaminofluorescein (DAF) nitrosation in the presence of PTIO and DPTA-NO showed that optimal PTIO concentrations required for maximal N(2)O(3) synthesis and for highest IL-8 gene expression are similar. 4,5-diaminofluorescein 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 15311945-7 2004 Analysis of 4,5-diaminofluorescein (DAF) nitrosation in the presence of PTIO and DPTA-NO showed that optimal PTIO concentrations required for maximal N(2)O(3) synthesis and for highest IL-8 gene expression are similar. dpta-no 81-88 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 15478484-1 2004 PURPOSE: To evaluate the effectiveness of a 5% sodium fluoride (NaF) bioerodible gel to remineralize demineralized enamel. Sodium Fluoride 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 15356918-0 2004 Stimulation of endothelial IL-8 (eIL-8) production and apoptosis by phenolic metabolites of benzene in HL-60 cells and human bone marrow endothelial cells. Benzene 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15356918-2 2004 One potential mechanism of apoptosis induced by benzene metabolites that has not been examined is the production of pro-apoptotic cytokines such as endothelial IL-8 from endothelial cells in bone marrow stroma. Benzene 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 15072962-0 2004 Cytokine gene expression in human skeletal muscle during concentric contraction: evidence that IL-8, like IL-6, is influenced by glycogen availability. Glycogen 129-137 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 15072962-6 2004 In addition, the fold change for both IL-8 and IL-6 was markedly higher (P < 0.05) in Lo Gly compared with Con. Glycine 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 15072962-11 2004 Furthermore, the mRNA abundance of IL-6 and IL-8 appears to be influenced by glycogen availability in the contracting muscle. Glycogen 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 15271731-2 2004 We investigated the hypothesis that epidural clonidine premedication and postoperative patient-controlled epidural analgesia (PCEA) including clonidine would decrease the release of proinflammatory (interleukin (IL)-6, IL-1beta, IL-8, and tumor necrosis factor (TNF)-alpha) and antiinflammatory (IL-1 receptor antagonist (RA)) cytokines in patients who underwent elective colorectal surgery and that they would provide better postoperative analgesia. Clonidine 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 229-233 15305018-7 2004 A strong inhibition of the expression of the cytokine IL-8 by cultured neutrophils was also observed; this is discussed with reference to the antioxidant-like property of acetoacetate. acetoacetic acid 171-183 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 15271731-2 2004 We investigated the hypothesis that epidural clonidine premedication and postoperative patient-controlled epidural analgesia (PCEA) including clonidine would decrease the release of proinflammatory (interleukin (IL)-6, IL-1beta, IL-8, and tumor necrosis factor (TNF)-alpha) and antiinflammatory (IL-1 receptor antagonist (RA)) cytokines in patients who underwent elective colorectal surgery and that they would provide better postoperative analgesia. Clonidine 142-151 C-X-C motif chemokine ligand 8 Homo sapiens 229-233 15271731-6 2004 For patients in the clonidine group, production of IL-1RA, IL-6, and IL-8 was significantly less increased at the end of the surgical procedure and at 12 and 24 h after surgery. Clonidine 20-29 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 15283562-5 2004 After reaction with hydrofluoric acid (HF) or fluoride salts (KF, CsF, NaF), its immunoreactivity is restored, and native estradiol is formed and is detected by immunoassay. Hydrofluoric Acid 20-37 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 15283562-5 2004 After reaction with hydrofluoric acid (HF) or fluoride salts (KF, CsF, NaF), its immunoreactivity is restored, and native estradiol is formed and is detected by immunoassay. Fluorides 46-60 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 15283562-5 2004 After reaction with hydrofluoric acid (HF) or fluoride salts (KF, CsF, NaF), its immunoreactivity is restored, and native estradiol is formed and is detected by immunoassay. Estradiol 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 15302609-6 2004 Urinary IL-8 levels of MIBC patients were significantly increased when compared with the levels of SBC patients and healthy subjects (P < 0.001). 4-METHYL-2-PENTANOL 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 15297094-0 2004 Glutamine and CXC chemokines IL-8, Mig, IP-10 and I-TAC in human intestinal epithelial cells. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 15297094-4 2004 METHODS: The present study aimed to determine the effect of glutamine on the IL-8, Mig, IP-10 and I-TAC production by ELISA and their mRNA level by RT-PCR (expressed as % gapdh) in two human intestinal epithelial cell lines Caco-2/TC7 and HCT-8 under basal conditions or during stimulation with combined cytokines. Glutamine 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15265937-3 2004 We recently reported that heme is a proinflammatory molecule, able to induce neutrophil migration, reactive oxygen species generation, and IL-8 expression. Heme 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 15259026-2 2004 The transcriptional profile induced by IL-8 in human neutrophils was analyzed using high-density oligonucleotide arrays and compared with that of the prototypic phagocyte activator LPS. density oligonucleotide 89-112 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 15518173-0 2004 Inhibitory effect of water-soluble chitosan on TNF-alpha and IL-8 secretion from HMC-1 cells. Water 21-26 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15518173-3 2004 In this study, we investigated whether pro-inflammatory cytokines (TNF-alpha and IL-8) can be induced by calcium stimulation in HMC-1 cells, and high molecular weight water-soluble chitosan (WSC) can inhibit the production of these cytokines. Calcium 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 15297492-0 2004 Alanine-threonine polymorphism of Helicobacter pylori RpoB is correlated with differential induction of interleukin-8 in MKN45 cells. Alanine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 15297492-0 2004 Alanine-threonine polymorphism of Helicobacter pylori RpoB is correlated with differential induction of interleukin-8 in MKN45 cells. Threonine 8-17 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 15297492-6 2004 RpoB(Thr) strains induced a much larger amount of interleukin-8, a chemokine that plays an important role in chronic inflammation, than RpoB(Ala) strains in cultured MKN45 cells. Threonine 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 15518173-4 2004 We provided evidence that the secretion of TNF-alpha and IL-8 from HMC-1 cells was induced by Ca2+-ionophore A23187 or Ca2+-ATPase inhibitor TSG. Calcimycin 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 15518173-6 2004 IL-8 secretion in response to A23187 or TSG was inhibited by 49.2% for A23187 and 34.1% for TSG, respectively, compared to absence of WSC. Calcimycin 30-36 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15518173-6 2004 IL-8 secretion in response to A23187 or TSG was inhibited by 49.2% for A23187 and 34.1% for TSG, respectively, compared to absence of WSC. Calcimycin 71-77 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15265658-10 2004 Poly I:C treatment of RPE resulted in an increase in the production of IL-6, IL-8, MCP-1, and sICAM-1. Poly I-C 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 15194816-8 2004 The stretch-induced augmentation of both IL-8 and MCP-3 expression was significantly suppressed by an activator protein-1 (AP-1) inhibitor, curcumin. Curcumin 140-148 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 15300205-9 2004 RESULTS: beta-glucan significantly enhanced chemotaxis toward C5a and suppressed that toward IL-8 in a CR3-dependent fashion. beta-Glucans 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 15302158-3 2004 We have shown that stimulation of the human B cell line RPMI 8226 with CpG-ODN 1826 or 2006 results in the activation of IL-8 promoter and nuclear localization of NF-kappaB in the CG sequence- and phosphorothioate backbone modification-dependent manner. Parathion 197-213 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 15344533-4 2004 The production of IL-8 from esophageal mucosal cells was enhanced by the exposure to bile acid. Bile Acids and Salts 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 15258595-3 2004 Dendrimer glucosamine inhibited Toll-like receptor 4-mediated lipopolysaccharide induced synthesis of pro-inflammatory chemokines (MIP-1 alpha, MIP-1 beta, IL-8) and cytokines (TNF-alpha, IL-1 beta, IL-6) from human dendritic cells and macrophages but allowed upregulation of the costimulatory molecules CD25, CD80, CD83 and CD86. Glucosamine 10-21 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 15181190-2 2004 We have shown that recombinant human IL-8/CXCL8 (rhIL-8/CXCL8) protects cultured IEC against tumor necrosis factor (TNF)-alpha and cycloheximide-induced cytotoxicity. Cycloheximide 131-144 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 15181190-2 2004 We have shown that recombinant human IL-8/CXCL8 (rhIL-8/CXCL8) protects cultured IEC against tumor necrosis factor (TNF)-alpha and cycloheximide-induced cytotoxicity. Cycloheximide 131-144 C-X-C motif chemokine ligand 8 Homo sapiens 42-47 15181190-2 2004 We have shown that recombinant human IL-8/CXCL8 (rhIL-8/CXCL8) protects cultured IEC against tumor necrosis factor (TNF)-alpha and cycloheximide-induced cytotoxicity. Cycloheximide 131-144 C-X-C motif chemokine ligand 8 Homo sapiens 56-61 15349669-5 2004 Analysis of the thin section by SEM after exposure to dentifrices showed that NaF/SiO(2) produced significant remineralization whereas MFP/CaCO(3) system resulted in little remineralization. Silicon Dioxide 82-88 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 15300205-10 2004 In the competing chemotactic gradient assays (C5a vs IL-8), beta-glucan further enhanced migration toward C5a while not affecting that toward IL-8. beta-Glucans 60-71 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 15300205-11 2004 CONCLUSIONS: beta-glucan selectively upregulates PMN chemotaxis toward C5a while suppressing chemotaxis toward IL-8. beta-Glucans 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 15143062-0 2004 Oxidized phospholipids increase interleukin 8 (IL-8) synthesis by activation of the c-src/signal transducers and activators of transcription (STAT)3 pathway. Phospholipids 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 15219825-6 2004 Eotaxin stimulated IL-8 production, which was inhibited by AG1478. RTKI cpd 59-65 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 15242697-3 2004 Steroids modulate some plasma cytokines (decreasing TNFalpha, IL-8, IL-6 and increasing IL-10), whereas ability to reduce plasma and urinary TNFsr-2 and IL-1ra and peri-operative renal injury is unknown. Steroids 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 15133028-2 2004 Glu-Leu-Arg ("ELR") CXC chemokines interleukin-8 (IL-8) and melanoma growth stimulatory activity (MGSA) recruit neutrophils by binding and activating two receptors, CXCR1 and CXCR2. Glu-Leu-Arg 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 15133028-2 2004 Glu-Leu-Arg ("ELR") CXC chemokines interleukin-8 (IL-8) and melanoma growth stimulatory activity (MGSA) recruit neutrophils by binding and activating two receptors, CXCR1 and CXCR2. Glu-Leu-Arg 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 15087294-7 2004 Dexamethasone suppressed LPS-induced granulocyte macrophage-colony stimulating factor, tumor necrosis factor-alpha, and interleukin-8 release by 83 +/- 1%, 51 +/- 7% and 20 +/- 9% (p < 0.001), respectively. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 15087294-8 2004 Similar effects were seen on nuclear factor-kappaB inhibition, and interleukin-8 release was further reduced by the HDAC enhancer, theophylline (37 +/- 6%). Theophylline 131-143 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 15143062-0 2004 Oxidized phospholipids increase interleukin 8 (IL-8) synthesis by activation of the c-src/signal transducers and activators of transcription (STAT)3 pathway. Phospholipids 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 15256456-0 2004 Expression of angiogenic factors vascular endothelial growth factor and interleukin-8/CXCL8 is highly responsive to ambient glutamine availability: role of nuclear factor-kappaB and activating protein-1. Glutamine 124-133 C-X-C motif chemokine ligand 8 Homo sapiens 72-85 15256456-0 2004 Expression of angiogenic factors vascular endothelial growth factor and interleukin-8/CXCL8 is highly responsive to ambient glutamine availability: role of nuclear factor-kappaB and activating protein-1. Glutamine 124-133 C-X-C motif chemokine ligand 8 Homo sapiens 86-91 15240713-7 2004 Stimulation of the above-mentioned cells with bacterial DNA or CpG oligodeoxynucleotide resulted in an inflammatory reaction characterized by a dose-dependent up-regulation of cytokines (IL-6, IL-8) and human beta-defensin 2. Oligodeoxyribonucleotides 67-87 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 15240743-4 2004 RAPBTL (n = 20) induced an up-regulation of ICAM-1, intracellular IL-8, IL-6, IL-15, and surface IL-15 in cocultured RASFibs. rapbtl 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 15256456-5 2004 VEGF and IL-8 secretion and mRNA levels were dramatically induced by glutamine deprivation. Glutamine 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 15240743-12 2004 In turn, these cytokines stimulate the expression of IL-15, IL-8, and IL-6 in RASFibs, thereby creating a feedback loop that favors persistent synovial inflammation. rasfibs 78-85 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 15207247-3 2004 In this report, we demonstrate, using two potent and selective inhibitors of MEK activation by Raf-1 (PD-098059) and p38 (SB-203580), that both ERK1/2 and p38 pathways play a key role in the production of IL-8 by porins and LPS. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 102-111 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 15207247-3 2004 In this report, we demonstrate, using two potent and selective inhibitors of MEK activation by Raf-1 (PD-098059) and p38 (SB-203580), that both ERK1/2 and p38 pathways play a key role in the production of IL-8 by porins and LPS. SB 203580 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 15207247-4 2004 Porin-stimulated expression of activating protein 1 (AP-1) and correlated IL-8 release is also inhibited by PD-098059 or SB-203580 indicating that the Raf-1/MEK1-MEK2/MAPK cascade is required for their activation. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15207247-4 2004 Porin-stimulated expression of activating protein 1 (AP-1) and correlated IL-8 release is also inhibited by PD-098059 or SB-203580 indicating that the Raf-1/MEK1-MEK2/MAPK cascade is required for their activation. SB 203580 121-130 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 15207247-5 2004 Also PTKs modulate the pathway that control IL-8 gene expression, in fact its expression is abolished by tyrphostin. Tyrphostins 105-115 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 15223398-5 2004 RESULTS: Polyvinylchloride induced a substantial increase in IL-8 and MCP-1, which was abolished by cycloheximide, indicating that they were synthesized during incubation. Polyvinyl Chloride 9-26 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15111623-9 2004 Furthermore, addition of the peptide, comprising the surface loop between Cys(95) and Cys(105), predicted by model, particularly in oxidized form, decreased LPS-induced production of tumor necrosis factor alpha and interleukin-8 upon application to monocytic cells and fibroblasts, respectively, supporting its involvement in LPS signaling. Cysteine 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 215-228 15111623-9 2004 Furthermore, addition of the peptide, comprising the surface loop between Cys(95) and Cys(105), predicted by model, particularly in oxidized form, decreased LPS-induced production of tumor necrosis factor alpha and interleukin-8 upon application to monocytic cells and fibroblasts, respectively, supporting its involvement in LPS signaling. Cysteine 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 215-228 15223398-8 2004 Heparin-coated polyvinylchloride efficiently prevented synthesis of both IL-8 and MCP-1. Heparin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 15223398-8 2004 Heparin-coated polyvinylchloride efficiently prevented synthesis of both IL-8 and MCP-1. Polyvinyl Chloride 15-32 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 15223398-9 2004 Addition of recombinant human complement factor 5a to blood incubated in heparin-coated polyvinylchloride restored IL-8 and MCP-1 production completely and partly, respectively. Heparin 73-80 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15223398-9 2004 Addition of recombinant human complement factor 5a to blood incubated in heparin-coated polyvinylchloride restored IL-8 and MCP-1 production completely and partly, respectively. Polyvinyl Chloride 88-105 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 15223398-13 2004 CONCLUSIONS: Polyvinylchloride induced a marked increase in IL-8 and MCP-1, in contrast to a marginal increase in tumor necrosis factor alpha, IL-1 beta, IL-6, and IL-10. Polyvinyl Chloride 13-30 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 15223398-14 2004 The increase in IL-8 and MCP-1 was prevented by heparin-coated polyvinylchloride. Heparin 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15223398-14 2004 The increase in IL-8 and MCP-1 was prevented by heparin-coated polyvinylchloride. coated polyvinylchloride 56-80 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 15196211-4 2004 In response to zymosan and flagellin, pathogen-associated molecular patterns (PAMP) that are recognized by TLR2 and TLR5 respectively, ECC-1 cells secreted significantly more IL-8, MCP-1 and IL-6 than in response to other TLR agonists. Zymosan 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 15240502-11 2004 The inhibition of the activity of phosphoinositide-3 kinase (PI3K) with wortmannin showed that 72%-80% of the rate of pseudopod extension induced with N-formyl-methionyl-leucyl-phenylalanine, platelet activating factor, and leukotriene B4 was phosphoinositide-3 kinase-dependent, in contrast to 55% of the rate of pseudopod extension induced with interleukin-8. Wortmannin 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 347-360 15293603-4 2004 Inhibition of proteasome activity by ALLN and beta-lactone resulted in significantly increased IL-8 secretion (5- to 22-fold). beta-Lactone 46-58 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 15384255-0 2004 Bleomycin induces IL-8 and ICAM-1 expression in microvascular pulmonary endothelial cells. Bleomycin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 15384255-5 2004 Finally, pre-treatment with a selective p38 MAPK-inhibitor, SB 203580, potently reduced the BLM-induced up-regulation of IL-8 expression but did not show any effect on expression of ICAM-1. SB 203580 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 15316216-11 2004 Stimulation with CS resulted in upregulation of mRNA for IL-6 and IL-8 and protein release. Cesium 17-19 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 15190028-7 2004 RESULTS: Lag phase S. pneumoniae treated at sub-MIC (1/8 MIC) cefotaxime or faropenem induced 11-fold and 8-fold increases, respectively, in TLR2-mediated IL-8 promoter activity when compared with untreated bacteria. Cefotaxime 62-72 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 15190028-7 2004 RESULTS: Lag phase S. pneumoniae treated at sub-MIC (1/8 MIC) cefotaxime or faropenem induced 11-fold and 8-fold increases, respectively, in TLR2-mediated IL-8 promoter activity when compared with untreated bacteria. fropenem 76-85 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 15178710-0 2004 Nitric oxide post-transcriptionally up-regulates LPS-induced IL-8 expression through p38 MAPK activation. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 15178710-8 2004 In THP-1 cells and human primary monocytes treated with actinomycin D, NO(.-) had no effect on TNF-alpha mRNA stability (P>0.3 for both cell types) but significantly stabilized IL-8 mRNA (P=0.001 for both cell types). Dactinomycin 56-69 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 15178710-10 2004 Further, SB202190, a p38 MAPK inhibitor, was shown to block NO(.-)-induced stabilization of IL-8 mRNA (P<0.02 for both cell types). 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 15178710-12 2004 IL-8 mRNA stabilization by NO(.-) is independent of cGMP and at least partially dependent on p38 MAPK activation. Cyclic GMP 52-56 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15028780-6 2004 Furthermore, the CXCR2-specific antagonist SB225002 [N-(2-hydroxy-4-nitrophenyl)-N"-(2-bromophenyl)urea] is 10-fold more potent in inhibiting IL-8 binding to hCXCR2 than to cCXCR2, suggesting that some of the observed differences in the amino acid sequences of the human and monkey receptor affect ligand binding sites or the conformation of the receptor. SB 225002 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 15028780-6 2004 Furthermore, the CXCR2-specific antagonist SB225002 [N-(2-hydroxy-4-nitrophenyl)-N"-(2-bromophenyl)urea] is 10-fold more potent in inhibiting IL-8 binding to hCXCR2 than to cCXCR2, suggesting that some of the observed differences in the amino acid sequences of the human and monkey receptor affect ligand binding sites or the conformation of the receptor. SB 225002 53-103 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 15121876-11 2004 Exposure to mifepristone made the spatial difference in IL-8 disappear and increased the expression of TNFalpha in the epithelium of the isthmus, but had no effect on the expression of TGFbeta1 or LIF. Mifepristone 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 15162381-9 2004 Quantitative assay of BPH tissue extracts revealed that tissue IL-8 levels are correlated with both SA-beta gal activity and prostate weight. 2-(2-quinolinyl)-1H-indene--1,3(2H)-dione-6'-sulfonic acid 100-111 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 15201697-14 2004 The ratios of IL-6 to IL-10 and IL-8 to IL-10 were significantly lower in DZX groups than in controls (P = 0.025 and P = 0.041 for each, respectively). Diazoxide 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 15137059-8 2004 Cytochalasin D also activated p38 MAP kinase, which pathway contributed to the cytochalasin D-induced increase in IL-8 production. Cytochalasin D 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 15137059-8 2004 Cytochalasin D also activated p38 MAP kinase, which pathway contributed to the cytochalasin D-induced increase in IL-8 production. Cytochalasin D 79-93 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 15075332-4 2004 Likewise, treatment of cells with NaF (an inhibitor of protein phosphatases) allowed for phosphorylation of Ser-985, and a protein phosphatase responsible for dephosphorylation of Ser-985 was identified to be protein phosphatase 2A (PP2A). Serine 108-111 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 15213840-7 2004 The EGFR kinase inhibitor tyrphostin AG1478 abrogated the TF/FVIIa-complex induced MAP kinase activation and mRNA increase of egr-1, heparin-binding EGF, and interleukin-8 following FVIIa addition. Tyrphostins 26-36 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 15213840-7 2004 The EGFR kinase inhibitor tyrphostin AG1478 abrogated the TF/FVIIa-complex induced MAP kinase activation and mRNA increase of egr-1, heparin-binding EGF, and interleukin-8 following FVIIa addition. RTKI cpd 37-43 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 15269990-9 2004 CONCLUSION: During cardiac surgery (mitral valve replacement) PGE1 may suppressed the production of IL-6, IL-8 but not IL-10, which may be related to its myocardial protection effect. Alprostadil 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 15075332-4 2004 Likewise, treatment of cells with NaF (an inhibitor of protein phosphatases) allowed for phosphorylation of Ser-985, and a protein phosphatase responsible for dephosphorylation of Ser-985 was identified to be protein phosphatase 2A (PP2A). Serine 180-183 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 15155343-9 2004 TCV-309 significantly inhibited the production of TNF, IL-6, and IL-8 induced by LPS, SEB, and bacteria. TCV 309 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 15187156-4 2004 The adenosine analog 5"-N-ethylcarboxamidoadenosine (NECA) (10 microM) increased mRNA expression of IL-1beta, IL-3, IL-4, IL-8, and IL-13, but not IL-2 and IFN-gamma. Adenosine 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15187156-4 2004 The adenosine analog 5"-N-ethylcarboxamidoadenosine (NECA) (10 microM) increased mRNA expression of IL-1beta, IL-3, IL-4, IL-8, and IL-13, but not IL-2 and IFN-gamma. Adenosine-5'-(N-ethylcarboxamide) 21-51 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15187156-4 2004 The adenosine analog 5"-N-ethylcarboxamidoadenosine (NECA) (10 microM) increased mRNA expression of IL-1beta, IL-3, IL-4, IL-8, and IL-13, but not IL-2 and IFN-gamma. Adenosine-5'-(N-ethylcarboxamide) 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 15188490-3 2004 HHcy unleashes mediators of inflammation such as NFkappaB, IL-1beta, IL-6, and IL-8, increases production of intracellular superoxide anion causing oxidative stress and reducing intracellular level of nitric oxide (NO), and induces endoplasmic reticulum (ER) stress which can explain many processes of Hcy-promoted cell injury such as apoptosis, fat accumulation, and inflammation. Homocysteine 1-4 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 15147461-0 2004 Interleukin-8 and RANTES levels in patients with relapsing-remitting multiple sclerosis (RR-MS) treated with cladribine. Cladribine 109-119 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 15147461-5 2004 RESULTS: After Cladribine treatment the levels of IL-8 decreased significantly in CSF only, whereas the RANTES levels decreased significantly both in CSF and serum. Cladribine 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 15136298-3 2004 We therefore studied the effect of a new thiol antioxidant compound, Nacystelyn (NAL), on IL-8 regulation in a human macrophage-derived cell line (THP-1). N-acetylcysteine lysinate 69-79 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 15136298-3 2004 We therefore studied the effect of a new thiol antioxidant compound, Nacystelyn (NAL), on IL-8 regulation in a human macrophage-derived cell line (THP-1). N-acetylcysteine lysinate 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 15155187-1 2004 We previously showed that moxifloxacin (MXF) exerts protective anti-inflammatory effects in immunosuppressed mice infected with Candida albicans by inhibiting interleukin-8 (IL-8) and tumor necrosis factor alpha (TNF-alpha) production in the lung. Moxifloxacin 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 15155187-1 2004 We previously showed that moxifloxacin (MXF) exerts protective anti-inflammatory effects in immunosuppressed mice infected with Candida albicans by inhibiting interleukin-8 (IL-8) and tumor necrosis factor alpha (TNF-alpha) production in the lung. Moxifloxacin 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 15155187-3 2004 In the present study we investigated the effects of MXF on the production of proinflammatory cytokines (i.e., IL-8, TNF-alpha, and IL-1beta) by activated human peripheral blood monocytes and THP-1 cells and analyzed the effects of the drug on the major signal transduction pathways associated with inflammation: NF-kappaB and the mitogen-activated protein kinases ERK and c-Jun N-terminal kinase (JNK). Moxifloxacin 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 15166955-5 2004 RESULTS: Gene array analysis from LCM-dissected tissues demonstrated: (i) increased expression of interleukin-8 (IL-8), an activator of the inflammatory factor nuclear factor-kappaB (NF-kappaB), and (ii) decreased expression of IkappaB (an inhibitor of NF-kappaB) in CP ductal cells compared with normal ducts. ikappab 228-235 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 15166955-5 2004 RESULTS: Gene array analysis from LCM-dissected tissues demonstrated: (i) increased expression of interleukin-8 (IL-8), an activator of the inflammatory factor nuclear factor-kappaB (NF-kappaB), and (ii) decreased expression of IkappaB (an inhibitor of NF-kappaB) in CP ductal cells compared with normal ducts. ikappab 228-235 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 15196286-13 2004 Levocetirizine significantly reduced eosinophils (P=0.029), neutrophils (P=0.005), IL-4 (P=0.041), and IL-8 (P=0.02), whereas desloratadine diminished IL-4 only (P=0.044). levocetirizine 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 15136050-0 2004 Aspirin inhibits monocyte chemoattractant protein-1 and interleukin-8 expression in TNF-alpha stimulated human umbilical vein endothelial cells. Aspirin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 15136050-6 2004 In this study, we found that aspirin inhibited TNF-alpha (10 ng/ml)-induced MCP-1 and IL-8 expression at the RNA and protein levels in human umbilical vein endothelial cells (HUVECs), monocyte adhesion and transmigration, and that its inhibitory effects were not due to decreased HUVEC viability as assessed by MTT test. Aspirin 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 15136050-7 2004 Aspirin at the dose as low as 10 microg/ml significantly inhibited the release of TNF-stimulated MCP-1 by 29.1% (P = 0.008) and IL-8 by 26.9% (P = 0.0146) as compared to TNF-stimulated release. Aspirin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 15136050-11 2004 These results in our study suggest that aspirin inhibits TNF-alpha stimulated MCP-1 and IL-8 release in HUVECs, for its additional therapeutic effects of aspirin in causing atherosclerosis. Aspirin 40-47 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 15235923-14 2004 Monocytes or neutrophils exposed to urate crystals produce tumor necrosis factor alpha, interleukin-1 (IL-1), IL-6, and IL-8. Uric Acid 36-41 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 15218990-3 2004 IL-8 production was dependent on phosphorylation of ERK-1 and -2 and p38 MAPK, as examined by PD 098059 (10 microM), an inhibitor of the upstream activator of MAPK kinase (MKK)-1, and SB 203580 (10 microM), an inhibitor of p38 MAPK. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 94-103 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15329007-6 2004 Cetirizine treatment induced a significant decrease of IL4 (p<0.01) and IL8 levels (p=0.01). Cetirizine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 14717657-0 2004 Methotrexate induces interleukin-8 production by human bronchial and alveolar epithelial cells. Methotrexate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 14717657-5 2004 To elucidate the proinflammatory mechanism of MTX-induced pneumonitis, we evaluated the effect of MTX on the production of IL (interleukin)-8 by human bronchial and alveolar epithelial cells in vitro and the role of p38 MAPK (mitogen-activated protein kinase) in order to clarify the intracellular signal regulating IL-8 expression. Methotrexate 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 123-141 14717657-5 2004 To elucidate the proinflammatory mechanism of MTX-induced pneumonitis, we evaluated the effect of MTX on the production of IL (interleukin)-8 by human bronchial and alveolar epithelial cells in vitro and the role of p38 MAPK (mitogen-activated protein kinase) in order to clarify the intracellular signal regulating IL-8 expression. Methotrexate 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 123-141 14717657-6 2004 MTX induced IL-8 secretion by human bronchial and alveolar epithelial cells in a dose- and time-dependent manner within the range of the clinically observed serum concentrations. Methotrexate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 14717657-8 2004 SB203580, the specific inhibitor of p38 MAPK, inhibited MTX-induced IL-8 production. SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 14717657-8 2004 SB203580, the specific inhibitor of p38 MAPK, inhibited MTX-induced IL-8 production. Methotrexate 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 14717657-10 2004 These results suggest that MTX activates bronchial and alveolar epithelial cells to induce IL-8 production through p38 MAPK, which might play an important role as one of the mechanisms of MTX-induced lung inflammation. Methotrexate 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 14717657-10 2004 These results suggest that MTX activates bronchial and alveolar epithelial cells to induce IL-8 production through p38 MAPK, which might play an important role as one of the mechanisms of MTX-induced lung inflammation. Methotrexate 188-191 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 15218990-3 2004 IL-8 production was dependent on phosphorylation of ERK-1 and -2 and p38 MAPK, as examined by PD 098059 (10 microM), an inhibitor of the upstream activator of MAPK kinase (MKK)-1, and SB 203580 (10 microM), an inhibitor of p38 MAPK. SB 203580 184-193 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15218990-6 2004 Lipopolysaccharide-induced IL-8 production was dependent on activation of NF-kappaB, as examined by SN 50 (100 microM), an inhibitor of NF-kappaB translocation, and the specific NF-kappaB inhibitor kinase-2 inhibitor, AS 602868 (10 microM), with no differences in AMs from smokers and nonsmokers. sn 50 100-105 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 15147563-2 2004 Here we show that triggering of the formyl peptide receptor (FPR) with f-Met-Leu-Phe (fMLF) substantially reduced the neutrophil superoxide production induced by activation of the CXC receptors with IL-8. Superoxides 129-139 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 15020655-1 2004 We previously reported that disaccharides (DS), generated by enzymatic degradation of heparin or heparan sulfate, inhibit T cell-mediated immune reactions in rodents and regulate cytokine [tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-8, and IL-1beta] secretion by T cells, macrophages, or intestinal epithelial cells. Disaccharides 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 230-248 15123733-3 2004 Previously, we have shown that short exposure of primary cutaneous melanoma cells to dacarbazine resulted in the upregulation of interleukin-8 (IL-8) and vascular endothelial growth factor (VEGF). Dacarbazine 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 129-142 15123733-3 2004 Previously, we have shown that short exposure of primary cutaneous melanoma cells to dacarbazine resulted in the upregulation of interleukin-8 (IL-8) and vascular endothelial growth factor (VEGF). Dacarbazine 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 15123733-12 2004 We propose that combination treatment with anti-VEGF/IL-8 or MEK inhibitors may potentiate the therapeutic effects of dacarbazine. Dacarbazine 118-129 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 14982951-7 2004 IL-1 receptor antagonist and to a lesser extent anti-TNF-alpha inhibited COBTB-induced CXCL8 secretion (P<0.01) but did not affect gene expression. cobtb 73-78 C-X-C motif chemokine ligand 8 Homo sapiens 87-92 15020655-1 2004 We previously reported that disaccharides (DS), generated by enzymatic degradation of heparin or heparan sulfate, inhibit T cell-mediated immune reactions in rodents and regulate cytokine [tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-8, and IL-1beta] secretion by T cells, macrophages, or intestinal epithelial cells. Disaccharides 43-45 C-X-C motif chemokine ligand 8 Homo sapiens 230-248 15153529-5 2004 Incubation of human intestinal epithelial HT-29 cells with DFO increased the expression of IL-8 mRNA, as well as the release of IL-8 protein. Deferoxamine 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 15153529-5 2004 Incubation of human intestinal epithelial HT-29 cells with DFO increased the expression of IL-8 mRNA, as well as the release of IL-8 protein. Deferoxamine 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 15153529-7 2004 Accordingly, the selective inhibitors for both kinases, either alone or in combination, completely abolished DFO-induced IL-8 secretion, indicating an importance of mitogen-activated protein kinases pathway. Deferoxamine 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 15153529-8 2004 These proinflammatory effects of DFO were, in large part, mediated by activation of Na(+)/H(+) exchangers, because selective blockade of Na(+)/H(+) exchangers prevented the DFO-induced IL-8 production. Deferoxamine 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 15153529-8 2004 These proinflammatory effects of DFO were, in large part, mediated by activation of Na(+)/H(+) exchangers, because selective blockade of Na(+)/H(+) exchangers prevented the DFO-induced IL-8 production. Deferoxamine 173-176 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 15147869-6 2004 We demonstrate that the induction of IL-8 expression by TWEAK can be counteracted by LiCl. Lithium Chloride 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 15046772-0 2004 Monophthalates promote IL-6 and IL-8 production in the human epithelial cell line A549. monophthalates 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 15120617-4 2004 TWEAK induced phosphorylation of IkappaBalpha and BAY11-7082, a selective inhibitor of IkappaBalpha phosphorylation, inhibited the TWEAK-induced IL-8 and GM-CSF production by BEAS2B cells. 3-(4-methylphenylsulfonyl)-2-propenenitrile 50-60 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 15135182-7 2004 In contrast to intact pyocyanin, oxidized pyocyanin was less efficient in NADH oxidation and stimulation of interleukin-8 release by human alveolar epithelial A549 cells in vitro, suggesting that oxidation of pyocyanin leads to its inactivation. Pyocyanine 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 15135182-7 2004 In contrast to intact pyocyanin, oxidized pyocyanin was less efficient in NADH oxidation and stimulation of interleukin-8 release by human alveolar epithelial A549 cells in vitro, suggesting that oxidation of pyocyanin leads to its inactivation. Pyocyanine 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 15120605-3 2004 The findings of this study show, for the first time, that the peroxisome proliferator-activated receptor (PPARalpha) agonist, fenofibrate, completely abolishes the LDL-induced IL-8 up-regulation at the transcriptional level. Fenofibrate 126-137 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 15082280-5 2004 RESULTS: Interleukin-8 and tumor necrosis factor-alpha levels after cardiopulmonary bypass were significantly lower in the aminophylline group than that in the control group (P < 0.05, for each group), and interleukin-10 level in aminophylline group was significantly higher than in control (P = 0.001). Aminophylline 123-136 C-X-C motif chemokine ligand 8 Homo sapiens 9-54 15136726-0 2004 Digitoxin mimics gene therapy with CFTR and suppresses hypersecretion of IL-8 from cystic fibrosis lung epithelial cells. Digitoxin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 15136726-3 2004 We show here that digitoxin, at sub nM concentrations, can suppress hypersecretion of IL-8 from cultured CF lung epithelial cells. Digitoxin 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 15136726-11 2004 We therefore suggest that digitoxin, with its lengthy history of human use, deserves consideration as a candidate drug for suppressing IL-8-dependent lung inflammation in CF. Digitoxin 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 15033544-10 2004 TNF-alpha and IL-1beta presented a maximum response after 1h treatment, while IL-6 and IL-8 maximum response was after 3h treatment. Tritium 119-121 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 15033544-16 2004 These data indicate that, Cd-induced TNF-alpha and IL-1beta, that probably, activate AP-1 transcription factor and IL-6 and IL-8 were induced. Cadmium 26-28 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 15168319-2 2004 This study was conducted to determine if treatment with the antioxidant melatonin would influence interleukin-6, interleukin-8, tumor necrosis factor alpha, and nitrite/nitrate levels in newborns with grade III or IV respiratory distress syndrome (radiographically confirmed) diagnosed within the first 6 hours of life. Melatonin 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 15168319-5 2004 Compared with the melatonin-treated respiratory distress syndrome newborns, in the untreated infants the concentrations of interleukin-6, interleukin-8, and tumor necrosis factor alpha were significantly higher at 24 hours, 72 hours, and at 7 days after onset of the study. Melatonin 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 138-151 15097437-0 2004 Effect of glutamine supplementation on diarrhea, interleukin-8 and secretory immunoglobulin A in children with acute diarrhea. Glutamine 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 15293554-4 2004 This study examined the effects of pyrrolidine dithiocarbamate (PDTC, 0.1 mM) and spermine NONOate (Sper-NO, 1 mM) on the secretion and gene expression of chemokines, interleukin (IL)-8, monocyte chemotactic protein (MCP)-1, regulated upon activation normal T cell expressed and secreted (RANTES), and eotaxin. spermine nitric oxide complex 82-98 C-X-C motif chemokine ligand 8 Homo sapiens 167-185 15124023-4 2004 Prevention of PBEF translation with an antisense oligonucleotide completely abrogates the inhibitory effects of LPS, IL-1, GM-CSF, IL-8, and TNF-alpha on neutrophil apoptosis. Oligonucleotides 49-64 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 15071361-0 2004 Azelnidipine, a newly developed long-acting calcium antagonist, inhibits tumor necrosis factor-alpha-induced interleukin-8 expression in endothelial cells through its anti-oxidative properties. azelnidipine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 109-122 15071361-0 2004 Azelnidipine, a newly developed long-acting calcium antagonist, inhibits tumor necrosis factor-alpha-induced interleukin-8 expression in endothelial cells through its anti-oxidative properties. Calcium 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 109-122 15071361-3 2004 In this study, we investigated whether and how azelnidipine, a newly developed long-acting calcium antagonist, could inhibit TNF-alpha-induced IL-8 expression in human umbilical vein endothelial cells (HUVEC). azelnidipine 47-59 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 15071361-6 2004 Further, azelnidipine was found to significantly inhibit activator protein-1 (AP-1) promoter activity and IL-8 expression in TNF-alpha-exposed HUVEC. azelnidipine 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 15071361-7 2004 An inhibitor of AP-1, curcumin, or an anti-oxidant, N-acetylcysteine, also inhibited the TNF-alpha-induced IL-8 expression in HUVEC. Curcumin 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 15071361-7 2004 An inhibitor of AP-1, curcumin, or an anti-oxidant, N-acetylcysteine, also inhibited the TNF-alpha-induced IL-8 expression in HUVEC. Acetylcysteine 52-68 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 15071361-8 2004 These results demonstrated that azelnidipine inhibited TNF-alpha-induced IL-8 expression in HUVEC by blocking NADPH oxidase-mediated ROS generation and subsequent AP-1 activation. azelnidipine 32-44 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 15071361-8 2004 These results demonstrated that azelnidipine inhibited TNF-alpha-induced IL-8 expression in HUVEC by blocking NADPH oxidase-mediated ROS generation and subsequent AP-1 activation. Reactive Oxygen Species 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 14730005-4 2004 Consistent with its ability to inhibit PLC-beta2 enzymatic activity, U73122 reduced interleukin-8 and leukotriene B(4)-induced Ca(2+) flux and chemotaxis in human neutrophils in a concentration-dependent manner. 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 69-75 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 15050605-5 2004 The p38 inhibitor SB 203580 resulted in a significant decrease in IL-8 peptide production (p < 0.01). SB 203580 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 15298427-0 2004 Methylprednisolone prevents inflammatory reaction occurring during cardiopulmonary bypass: effects on TNF-alpha, IL-6, IL-8, IL-10. Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 15050605-0 2004 Mechanism of glutamine-mediated amelioration of lipopolysaccharide-induced IL-8 production in Caco-2 cells. Glutamine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 15066049-3 2004 Previously, we found that melatonin reduced the rises in proinflammatory cytokines (IL-6, IL-8 and TNF-alpha) and nitrite/nitrate levels in the serum of preterm newborns with respiratory distress syndrome (RDS). Melatonin 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 15298427-12 2004 CONCLUSION: In this study, we have found that preoperative administration of methylprednisolone has decreased TNF-alpha, IL-6 and IL-8 release, and increased the perfusing IL-10 levels after CPB. Methylprednisolone 77-95 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 15050605-2 2004 We hypothesize that Gln down-regulates lipopolysaccharide (LPS)-stimulated IL-8 production in intestinal epithelial cells via transcription factors that counteract the effect of LPS-mediated increase in IL-8. Glutamine 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 15050605-9 2004 These results indicate that Gln deprivation enhances IL-8 production by Caco-2 cells after LPS stimulation and that down-regulation of IL-8 production with Gln is associated with alterations in STAT-4 transcription factor binding. Glutamine 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 15050605-2 2004 We hypothesize that Gln down-regulates lipopolysaccharide (LPS)-stimulated IL-8 production in intestinal epithelial cells via transcription factors that counteract the effect of LPS-mediated increase in IL-8. Glutamine 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 15050605-9 2004 These results indicate that Gln deprivation enhances IL-8 production by Caco-2 cells after LPS stimulation and that down-regulation of IL-8 production with Gln is associated with alterations in STAT-4 transcription factor binding. Glutamine 156-159 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 14722097-1 2004 The provision of glutamine in vivo has been observed to reduce to normal levels the neutrophilia observed after exhaustive exercise and to decrease the neutrophil chemoattractant, interleukin-8. Glutamine 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 15081272-7 2004 We found that exposure to soluble nickel sulfate results in the induction of hypoxia-inducible genes and IL-8 production by the 1HAEo(-) cells. nickel sulfate 34-48 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 15081272-8 2004 The simultaneous addition of iron in either ferric or ferrous form and nickel completely inhibited IL-8 production and had no effect on "hypoxia-like" stress caused by nickel, suggesting the existence of two different pathways for the induction "hypoxia-like" stress and IL-8 production. Iron 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 15081272-8 2004 The simultaneous addition of iron in either ferric or ferrous form and nickel completely inhibited IL-8 production and had no effect on "hypoxia-like" stress caused by nickel, suggesting the existence of two different pathways for the induction "hypoxia-like" stress and IL-8 production. Iron 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 271-275 15081272-8 2004 The simultaneous addition of iron in either ferric or ferrous form and nickel completely inhibited IL-8 production and had no effect on "hypoxia-like" stress caused by nickel, suggesting the existence of two different pathways for the induction "hypoxia-like" stress and IL-8 production. Nickel 71-77 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 15093669-6 2004 While vanadium deficiency accounts for several physiological malfunctionings including thyroid, glucose and lipid metabolism, etc., several genes are regulated by this element or by its compounds, which include genes for tumor necrosis factor-alpha (TNF-alpha), Interleukin-8 (IL-8), activator protein-1 (AP-1), ras, c-raf-1, mitogen activated protein kinase (MAPK), p53, nuclear factors-kappaB, etc. Vanadium 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 262-275 15093669-6 2004 While vanadium deficiency accounts for several physiological malfunctionings including thyroid, glucose and lipid metabolism, etc., several genes are regulated by this element or by its compounds, which include genes for tumor necrosis factor-alpha (TNF-alpha), Interleukin-8 (IL-8), activator protein-1 (AP-1), ras, c-raf-1, mitogen activated protein kinase (MAPK), p53, nuclear factors-kappaB, etc. Vanadium 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 277-281 15003325-6 2004 A marked increase in the levels of nitrite (as an index of NO) and IL-8 were observed in the NO2-exposed cells, which were further enhanced in the presence of the cytokines. Nitrogen Dioxide 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 15003325-10 2004 These results suggest a synergistic role of inflammatory mediators, particularly of NO and IL-8, in NO2-mediated early cellular changes. Nitrogen Dioxide 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 15089887-10 2004 Lansoprazole treatment significantly reduced the IL-8 mRNA expression levels. Lansoprazole 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 15084916-5 2004 When FLSs were co-cultured with CII-stimulated T cells, the production of interleukin-8, monocyte chemoattractant protein-1, and macrophage inflammatory protein-1alpha was significantly enhanced. N-[(1S)-2-methyl-1-(pyridin-4-ylcarbamoyl)propyl]cyclohexanecarboxamide 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 14656710-0 2004 Linoleic acid induces interleukin-8 production by Crohn"s human intestinal smooth muscle cells via arachidonic acid metabolites. Linoleic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 14656710-0 2004 Linoleic acid induces interleukin-8 production by Crohn"s human intestinal smooth muscle cells via arachidonic acid metabolites. Arachidonic Acid 99-115 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 14656710-1 2004 Previously we reported that linoleic acid (LA), but not oleic acid, caused a marked increase in the secretion of IL-8 by Crohn"s human intestinal smooth muscle (HISM) cells. Linoleic Acid 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 14656710-1 2004 Previously we reported that linoleic acid (LA), but not oleic acid, caused a marked increase in the secretion of IL-8 by Crohn"s human intestinal smooth muscle (HISM) cells. Oleic Acid 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 14656710-3 2004 In this study, we examined two mechanisms whereby LA, the dietary precursor for arachidonic acid (AA), could increase the production of IL-8 via activation of AA pathways: 1) by generation of reactive oxygen species by the AA-pathway enzymes to activate NF-kappaB or 2) by AA metabolites. Arachidonic Acid 80-96 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 14656710-3 2004 In this study, we examined two mechanisms whereby LA, the dietary precursor for arachidonic acid (AA), could increase the production of IL-8 via activation of AA pathways: 1) by generation of reactive oxygen species by the AA-pathway enzymes to activate NF-kappaB or 2) by AA metabolites. Reactive Oxygen Species 192-215 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 14656710-13 2004 Both Indo and NDGA blocked the IL-8 response to OxLA. Indomethacin 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 14656710-13 2004 Both Indo and NDGA blocked the IL-8 response to OxLA. oxla 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 14656710-15 2004 Similar to OxLA, OxAA stimulated production of IL-8 and AA metabolites. oxaa 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 15025932-5 2004 These oxidized phospholipids were shown to induce several proinflammatory genes, such as monocyte chemoattractant protein 1 or interleukin-8, and it is hypothesized that lipid oxidation products also play a role in other chronic inflammatory disorders. Phospholipids 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 127-140 14656710-16 2004 Pinane thromboxane, a selective thromboxane synthase inhibitor and receptor blocker, inhibited OxAA stimulation of TXB(2) and IL-8 in a dose-response manner. pinane thromboxane 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 14656710-17 2004 MK886, a selective 5-lipoxygenase inhibitor, inhibited OxAA stimulation of LTB(4) and IL-8 also in a dose-response manner. MK-886 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 15026281-0 2004 Acanthoic acid inhibits IL-8 production via MAPKs and NF-kappaB in a TNF-alpha-stimulated human intestinal epithelial cell line. acanthoic acid 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 15077296-6 2004 IL-8, MCP-1, and MIP-1 alpha levels in SF were strongly correlated with T cell responses to CII. N-[(1S)-2-methyl-1-(pyridin-4-ylcarbamoyl)propyl]cyclohexanecarboxamide 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15077296-7 2004 When FLS were cocultured with CII-stimulated T cells, the production of IL-8, MCP-1, and MIP-1 alpha was significantly increased. N-[(1S)-2-methyl-1-(pyridin-4-ylcarbamoyl)propyl]cyclohexanecarboxamide 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 15077296-10 2004 CONCLUSION: Our data indicate that the presence of CII-reactive T cells in RA joints can increase the production of chemokines such as IL-8, MCP-1, and MIP-1 alpha through interaction with FLS. N-[(1S)-2-methyl-1-(pyridin-4-ylcarbamoyl)propyl]cyclohexanecarboxamide 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 15077296-10 2004 CONCLUSION: Our data indicate that the presence of CII-reactive T cells in RA joints can increase the production of chemokines such as IL-8, MCP-1, and MIP-1 alpha through interaction with FLS. CHEMBL1232769 189-192 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 15452608-1 2004 In the complex with chitosan, lipopolysaccharide partially lost its ability to induce lymphokines tumor necrosis factor and interleukin-8, but retained immunostimulating properties and increased phagocytic function of macrophages by improving digestion of bacteria. Chitosan 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 15023565-0 2004 Native LDL induces interleukin-8 expression via H2O2, p38 Kinase, and activator protein-1 in human aortic smooth muscle cells. Hydrogen Peroxide 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 15023565-5 2004 METHODS AND RESULTS: LDL-induced IL-8 expression (mRNA and protein) is specific to SMCs and likely to be regulated at the transcription level in dose- and time-dependent manners, as judged by experiments with actinomycin D and ELISA. Dactinomycin 209-222 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 15023565-6 2004 Although both p38 and ERK 1/2 MAPKs were activated by LDL, only p38 MAPK is responsible for the LDL effects, as evidenced by a complete blockade of IL-8 upregulation by SB203580. SB 203580 169-177 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 15023565-7 2004 Pretreatment with catalase significantly decreased the extent of IL-8 upregulation, indicating that H2O2 is necessary for the LDL response. Hydrogen Peroxide 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 15023565-9 2004 CONCLUSIONS: These data demonstrated that LDL stimulates SMCs to induce IL-8 production in dose- and time-dependent manners at the transcription level and that the LDL signaling in hAoSMCs is conveyed via the generation of H2O2, the phosphorylation of p38 MAPK, the activation of AP-1, and the participation of NF-kappaB. Hydrogen Peroxide 223-227 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 15026281-4 2004 The aim of this study was to examine the inhibitory effect of acanthoic acid isolated from Acanthopanax koreanum (Araliaceae), on IL-8 production via mitogen-activated protein kinases (MAPKs) and nuclear factor-kappa B (NF-kappaB) in TNF-alpha-stimulated human colon epithelial cells. acanthoic acid 62-76 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 15026281-9 2004 RESULTS: Acanthoic acid suppressed TNF-alpha-induced IL-8 production in a dose-dependent manner. acanthoic acid 9-23 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 15026281-11 2004 CONCLUSION: Acanthoic acid might inhibit TNF-alpha-mediated IL-8 production by blocking in both the MAPKs and NF-kappaB pathways in HT29 cells. acanthoic acid 12-26 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 15056377-2 2004 The present study demonstrates that CXCL8 induces tyrosine phosphorylation as well as enzymatic activity of proline-rich tyrosine kinase 2 (Pyk2), a non-receptor protein tyrosine kinase (PTK), in human neutrophils. Tyrosine 50-58 C-X-C motif chemokine ligand 8 Homo sapiens 36-41 15068414-8 2004 Teprenone inhibited H. pylori-enhanced IL-8 production in MKN28 gastric epithelial cells in vitro, in a dose-dependent manner. geranylgeranylacetone 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 15068414-9 2004 CONCLUSIONS: Teprenone may modify corpus H. pylori-associated gastritis through its effect on neutrophil infiltration and H. pylori density, in part by its inhibition of IL-8 production in the gastric mucosa. geranylgeranylacetone 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 15056377-3 2004 Induction of Pyk2 tyrosine phosphorylation by CXCL8 is regulated by Src PTK activation, whereas it is unaffected by phosphatidylinositol 3-kinase activation. Tyrosine 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 46-51 14999747-5 2004 No significant difference between these three fluorides was observed although a general trend was seen where KF-treated PCL appeared to degrade slower than NaF-treated PCL which was slower than NH(4)F-treated PCL. polycaprolactone 168-171 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 15379216-5 2004 Ozone exposure (3.0 ppm, 3 min) time-dependently changed the redox state, while increasing production of interleukin(IL)-8 and IL-6, mRNA and protein. Ozone 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 105-122 15379216-6 2004 Treatment with GSH-OEt before ozone suppressed IL-8, but stimulated IL-6 production. S-ethyl glutathione 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 15005855-0 2004 Calcium signaling pathway involving calcineurin regulates interleukin-8 gene expression through activation of NF-kappaB in human osteoblast-like cells. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 15379213-2 2004 Intracellular levels of cytokine-induced IL-8 in human umbilical vein endothelial cells (HUVEC) were modulated using interferons and steroids to further elucidate their mechanism. Steroids 133-141 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 15379213-7 2004 Our study indicated that both, dexamethasone and IFN inhibit TNF-alpha-induced upregulation of IL-8 at the mRNA level. Dexamethasone 31-44 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 14999747-5 2004 No significant difference between these three fluorides was observed although a general trend was seen where KF-treated PCL appeared to degrade slower than NaF-treated PCL which was slower than NH(4)F-treated PCL. polycaprolactone 168-171 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 14999747-6 2004 Variation in solubilities of the salts was observed where the K(+) cation had the highest solubility and the Na(+) cation had the lowest solubility, which suggests that NaF was able to degrade the polymer more efficiently than the other fluorides. Fluorides 237-246 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 15031337-7 2004 Pre-incubation of the MC layer for 48 h with 55 mM glucose, a combination of two glucose degradation products, methylglyoxal and 3-deoxyglucosone, or conventional dialysis fluid (1:4 dilution), however, did not change the IL-8-induced migration of neutrophils. Methylcholanthrene 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 15115777-4 2004 We found that 2-arachidonoylglycerol induced a marked acceleration in the production of interleukin 8. glyceryl 2-arachidonate 14-36 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 15115777-6 2004 Augmented production of interleukin 8 was also observed with CP55940, a synthetic cannabinoid, and an ether-linked analog of 2-arachidonoylglycerol. 3-(2-hydroxy-4-(1,1-dimethylheptyl)phenyl)-4-(3-hydroxypropyl)cyclohexanol 61-68 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 15115777-6 2004 Augmented production of interleukin 8 was also observed with CP55940, a synthetic cannabinoid, and an ether-linked analog of 2-arachidonoylglycerol. Cannabinoids 82-93 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 15115777-6 2004 Augmented production of interleukin 8 was also observed with CP55940, a synthetic cannabinoid, and an ether-linked analog of 2-arachidonoylglycerol. Ether 102-107 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 15115777-6 2004 Augmented production of interleukin 8 was also observed with CP55940, a synthetic cannabinoid, and an ether-linked analog of 2-arachidonoylglycerol. glyceryl 2-arachidonate 125-147 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 15115777-9 2004 The accelerated production of interleukin 8 by 2-arachidonoylglycerol was observed not only in undifferentiated HL-60 cells, but also in HL-60 cells differentiated into macrophage-like cells. glyceryl 2-arachidonate 47-69 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 15115777-10 2004 Noticeably, 2-arachidonoylglycerol and lipopolysaccharide acted synergistically to induce the dramatically augmented production of interleukin 8. glyceryl 2-arachidonate 12-34 C-X-C motif chemokine ligand 8 Homo sapiens 131-144 15020194-7 2004 Nickel contact induced upregulation of MMP-2 and IL-8 mRNA production. Nickel 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 15020196-9 2004 SP administration decreased the release of interleukin (IL)-8 normally seen in keratinocytes after JP-8 exposure, a response similar to that reported for SP"s effect on JP-8 pulmonary toxicity. JP-8 99-103 C-X-C motif chemokine ligand 8 Homo sapiens 43-61 15019093-5 2004 The inhibitory effect of L-NIL was also observed on the PM2.5-induced interleukin-8 (IL-8) gene expression both at the transcriptional and protein levels. N(6)-(1-iminoethyl)lysine 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 15019093-5 2004 The inhibitory effect of L-NIL was also observed on the PM2.5-induced interleukin-8 (IL-8) gene expression both at the transcriptional and protein levels. N(6)-(1-iminoethyl)lysine 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 14670967-2 2004 In the current study, we demonstrated that LPA is a potent inducer of interleukin-6 (IL-6) and interleukin-8 (IL-8) production in ovarian cancer cells. lysophosphatidic acid 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 14670967-2 2004 In the current study, we demonstrated that LPA is a potent inducer of interleukin-6 (IL-6) and interleukin-8 (IL-8) production in ovarian cancer cells. lysophosphatidic acid 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 14670967-8 2004 Further, the effect of LPA on IL-6 and IL-8 generation is mediated by the Edg LPA receptors as enforced expression of LPA receptors restored LPA-induced IL-6 and IL-8 production in non-responsive cells and enhanced the sensitivity to LPA in responsive cell lines. lysophosphatidic acid 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 14670967-8 2004 Further, the effect of LPA on IL-6 and IL-8 generation is mediated by the Edg LPA receptors as enforced expression of LPA receptors restored LPA-induced IL-6 and IL-8 production in non-responsive cells and enhanced the sensitivity to LPA in responsive cell lines. lysophosphatidic acid 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 14670967-8 2004 Further, the effect of LPA on IL-6 and IL-8 generation is mediated by the Edg LPA receptors as enforced expression of LPA receptors restored LPA-induced IL-6 and IL-8 production in non-responsive cells and enhanced the sensitivity to LPA in responsive cell lines. lysophosphatidic acid 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 14670967-8 2004 Further, the effect of LPA on IL-6 and IL-8 generation is mediated by the Edg LPA receptors as enforced expression of LPA receptors restored LPA-induced IL-6 and IL-8 production in non-responsive cells and enhanced the sensitivity to LPA in responsive cell lines. lysophosphatidic acid 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 14670967-8 2004 Further, the effect of LPA on IL-6 and IL-8 generation is mediated by the Edg LPA receptors as enforced expression of LPA receptors restored LPA-induced IL-6 and IL-8 production in non-responsive cells and enhanced the sensitivity to LPA in responsive cell lines. lysophosphatidic acid 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 14670967-8 2004 Further, the effect of LPA on IL-6 and IL-8 generation is mediated by the Edg LPA receptors as enforced expression of LPA receptors restored LPA-induced IL-6 and IL-8 production in non-responsive cells and enhanced the sensitivity to LPA in responsive cell lines. lysophosphatidic acid 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 14670967-10 2004 These studies elucidate the transcriptional mechanism and the Edg LPA receptors involved in LPA-induced IL-6 and IL-8 production and suggest potential strategies to restrain the expression of these cytokines in ovarian cancer. lysophosphatidic acid 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 14712497-0 2004 Enhanced radiosensitization and chemosensitization in NF-kappaB-suppressed human oral cancer cells via the inhibition of gamma-irradiation- and 5-FU-induced production of IL-6 and IL-8. Fluorouracil 144-148 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 14993105-14 2004 Diosmectite exhibited a dose-dependent capacity to adsorb proteins in vitro as well as a dose-dependent inhibitory effect on the basolateral secretion of IL-8 by lipopolysaccharide (LPS)-stimulated HT29 cells. Smectite 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 14743348-3 2004 Agents that activate monocytes, including lipopolysacharrides (LPS), cytomegalovirus (CMV), and tumor necrosis factor (TNFalpha), have been shown to de-repress translation and these agents stabilize adhesion-induced transcripts for IL-lbeta and IL-8 and markedly diminish cell migration in the presence of autologous serum. lipopolysacharrides 42-61 C-X-C motif chemokine ligand 8 Homo sapiens 232-249 15041999-8 2004 Pretreatment of the ovarian cancer cells with the pertussis toxin completely inhibited lysophosphatidic acid-stimulated production of interleukin-6, interleukin-8 and tumor necrosis factor-alpha. lysophosphatidic acid 87-108 C-X-C motif chemokine ligand 8 Homo sapiens 149-194 14656946-0 2004 The bile acid deoxycholic acid (DCA) at neutral pH activates NF-kappaB and induces IL-8 expression in oesophageal cells in vitro. Bile Acids and Salts 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 14656946-0 2004 The bile acid deoxycholic acid (DCA) at neutral pH activates NF-kappaB and induces IL-8 expression in oesophageal cells in vitro. Deoxycholic Acid 14-30 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 14656946-0 2004 The bile acid deoxycholic acid (DCA) at neutral pH activates NF-kappaB and induces IL-8 expression in oesophageal cells in vitro. Deoxycholic Acid 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 14656946-6 2004 We show that physiological levels of DCA (100-300 microM) were capable of activating NF-kappaB in OE33 cells and inducing NF-kappaB target gene expression (particularly IkappaB and IL-8). Deoxycholic Acid 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 14977935-6 2004 Furthermore, an NF-kappaB inhibitor (pyrrolidine dithiocarbamate), a mitogen-activated protein (MAP) kinase (MEK) inhibitor (PD98059), and a p38 MAP kinase inhibitor (SB203580) significantly suppressed IL-8 synthesis in neutrophils. pyrrolidine dithiocarbamic acid 37-64 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 15037215-0 2004 Penta-O-galloyl-beta-D-glucose inhibits phorbol myristate acetate-induced interleukin-8 [correction of intereukin-8] gene expression in human monocytic U937 cells through its inactivation of nuclear factor-kappaB. penta-o-galloyl-beta-d-glucose 0-30 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 15037215-0 2004 Penta-O-galloyl-beta-D-glucose inhibits phorbol myristate acetate-induced interleukin-8 [correction of intereukin-8] gene expression in human monocytic U937 cells through its inactivation of nuclear factor-kappaB. Tetradecanoylphorbol Acetate 40-65 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 15037212-4 2004 Cetirizine, supposed to inhibit DNA binding activity of NF-kappa B, inhibits the expression of adhesion molecules on immunocytes and endothelial cells and the production of IL-8 and LTB4, two potent chemoattractants, by immune cells. Cetirizine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 14712497-7 2004 ELISA analysis indicated that although a remarkable increase in production of IL-6 and IL-8 was observed in B88 and B88neo after in vitro exposure to IR or treatment with 5-FU, radiotherapy and chemotherapy-induced production of these cytokines was significantly suppressed in B88mI cell clones. Fluorouracil 171-175 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 15037215-1 2004 We investigated the effects of the gallotannin penta-O-galloyl-beta-d-glucose (PGG) on interleukin (IL)-8 gene expression and nuclear factor (NF)-kappaB activation. gallotannin penta-o-galloyl-beta-d-glucose 35-77 C-X-C motif chemokine ligand 8 Homo sapiens 87-105 15187340-2 2004 Tacalcitol inhibited the mRNA expression and protein production of TPA-induced macrophage inflammatory protein-2 (MIP-2) and KC, the functional analogue of human interleukin (IL)-8, in the skin. 1 alpha,24-dihydroxyvitamin D3 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 162-180 15037215-1 2004 We investigated the effects of the gallotannin penta-O-galloyl-beta-d-glucose (PGG) on interleukin (IL)-8 gene expression and nuclear factor (NF)-kappaB activation. pgg 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 87-105 15037215-2 2004 PGG inhibited IL-8 production and gene expression in human monocytic U937 cells stimulated with phorbol myristate acetate (PMA), as measured by enzyme-linked immunosorbent assay and reverse transcription-polymerase chain reaction analysis, respectively. pgg 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 15037215-2 2004 PGG inhibited IL-8 production and gene expression in human monocytic U937 cells stimulated with phorbol myristate acetate (PMA), as measured by enzyme-linked immunosorbent assay and reverse transcription-polymerase chain reaction analysis, respectively. Tetradecanoylphorbol Acetate 96-121 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 15037215-2 2004 PGG inhibited IL-8 production and gene expression in human monocytic U937 cells stimulated with phorbol myristate acetate (PMA), as measured by enzyme-linked immunosorbent assay and reverse transcription-polymerase chain reaction analysis, respectively. Tetradecanoylphorbol Acetate 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 15037215-5 2004 PGG also inhibited both IL-8 production and NF-kappaB activation in the U937 cells stimulated with tumor necrosis factor-alpha. pgg 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 15037215-6 2004 These results suggest that PGG, a major constituent of the root cortex of Paeonia suffruticosa ANDREWS, can inhibit IL-8 gene expression by a mechanism involving its inhibition of NF-kappaB activation, which is dependent on I-kappaBalpha degradation. pgg 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 15001649-0 2004 Effects of thrombin, hypoxia, and steroids on interleukin-8 expression in decidualized human endometrial stromal cells: implications for long-term progestin-only contraceptive-induced bleeding. Steroids 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 15016021-8 2004 the control group used a sodium fluoride (NaF)-containing dentifrice and mouthrinse. Sodium Fluoride 25-40 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 15128054-10 2004 In 82 RAU patients with the serum IL-6 or IL-8 levels higher than the upper limit of normal serum concentration, treatment with levamisole for a period of 0.5-3.5 months could significantly reduce the serum IL-6 level from 12.0 +/- 1.6 to 3.0 +/- 0.5 pg/ml (P < 0.001), and could significantly lower the serum IL-8 level from 70.9 +/- 11.2 to 13.8 +/- 3.1 pg/ml (P < 0.001). Levamisole 128-138 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 15334993-9 2004 Addition of NaF or SnF2 resulted in higher fluoride release than the control group (p < 0.05). Fluorides 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 15334993-12 2004 Addition of NaF or SnF2 in an alginate impression material may result in effective release of fluoride without deteriorating the properties of material itself. Alginates 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 15334993-12 2004 Addition of NaF or SnF2 in an alginate impression material may result in effective release of fluoride without deteriorating the properties of material itself. Fluorides 94-102 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 15128054-10 2004 In 82 RAU patients with the serum IL-6 or IL-8 levels higher than the upper limit of normal serum concentration, treatment with levamisole for a period of 0.5-3.5 months could significantly reduce the serum IL-6 level from 12.0 +/- 1.6 to 3.0 +/- 0.5 pg/ml (P < 0.001), and could significantly lower the serum IL-8 level from 70.9 +/- 11.2 to 13.8 +/- 3.1 pg/ml (P < 0.001). Levamisole 128-138 C-X-C motif chemokine ligand 8 Homo sapiens 313-317 15128054-12 2004 Levamisole can modulate both the serum IL-6 and IL-8 levels in RAU patients. Levamisole 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 15128054-13 2004 IL-8, like IL-6, is also a useful serum marker in evaluating therapeutic effects of levamisole on RAU patients. Levamisole 84-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15026548-5 2004 Bortezomib also inhibited secretion of the proangiogenic factors matrix metalloproteinase-9, interleukin-8 (IL-8), and vascular endothelial growth factor (VEGF). Bortezomib 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 93-106 15034288-0 2004 [Deoxycholic acid-induced signal transduction in HT-29 cells: role of NF-kappa B and interleukin-8]. Deoxycholic Acid 1-17 C-X-C motif chemokine ligand 8 Homo sapiens 85-98 15034288-5 2004 Time and concentration courses of DCA-induced secretion of IL-8 were measured with ELISA in supernatants of cultured media from the cells. Deoxycholic Acid 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 15034288-7 2004 Moreover, DCA-induced secretions of IL-8 were measured after pretreatment with TUDC. Deoxycholic Acid 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 15034288-7 2004 Moreover, DCA-induced secretions of IL-8 were measured after pretreatment with TUDC. ursodoxicoltaurine 79-83 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 15034288-9 2004 The secretions of IL-8 were increased with DCA (50-200 micro M) treatment in a time and dose-dependent manner. Deoxycholic Acid 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 15034288-10 2004 Pre-incubation of the cells with TUDC (0.1-10 micro M) for 2 hours caused significant decreases in DCA induced IL-8 secretion. ursodoxicoltaurine 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 15034288-10 2004 Pre-incubation of the cells with TUDC (0.1-10 micro M) for 2 hours caused significant decreases in DCA induced IL-8 secretion. Deoxycholic Acid 99-102 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 15034288-12 2004 CONCLUSIONS: DCA may play as a colonic tumor promoter through anti-apoptotic effect of NF-kappa B activation and IL-8 expression, and DCA-induced NF-kappa B independent IL-8 expression is inhibited by TUDC. Deoxycholic Acid 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 15034288-12 2004 CONCLUSIONS: DCA may play as a colonic tumor promoter through anti-apoptotic effect of NF-kappa B activation and IL-8 expression, and DCA-induced NF-kappa B independent IL-8 expression is inhibited by TUDC. Deoxycholic Acid 134-137 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 15026559-0 2004 Correspondence re: DC Lev et al., Dacarbazine causes transcriptional up-regulation of interleukin 8 and vascular endothelial growth factor in melanoma cells: a possible escape mechanism from chemotherapy. Dacarbazine 34-45 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 15026548-5 2004 Bortezomib also inhibited secretion of the proangiogenic factors matrix metalloproteinase-9, interleukin-8 (IL-8), and vascular endothelial growth factor (VEGF). Bortezomib 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 15065641-5 2004 When plasmids encoding human IL8-glucagon 19-29 chimeric protein were injected into rats to evaluate the accuracy of this method, there was a high correlation between chimeric proteins measured by an enzyme-linked immunosorbent assay for human IL8 and one by a radioimmunoassay for glucagon. Glucagon 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 14982601-6 2004 Stretch-induced IL-8 and IL-6 production were significantly inhibited when intracellular GSH was further increased by NAC or GSH-e (P < 0.0001). Glutathione 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 14982601-6 2004 Stretch-induced IL-8 and IL-6 production were significantly inhibited when intracellular GSH was further increased by NAC or GSH-e (P < 0.0001). Acetylcysteine 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 14982601-6 2004 Stretch-induced IL-8 and IL-6 production were significantly inhibited when intracellular GSH was further increased by NAC or GSH-e (P < 0.0001). gsh-e 125-130 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 14982601-7 2004 Stretch-induced IL-8 and IL-6 production were augmented when intracellular GSH was depleted by BSO (P < 0.0001). Glutathione 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 14982601-8 2004 NAC blocked stretch-induced NF-kappa B and AP-1 binding and inhibited IL-8 mRNA expression. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 15162835-4 2004 Madimadi dose-dependently inhibited TNF-alpha, IL-1beta, and IL-8 production from activated human mast cells (HMC-1). madimadi 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 14984736-0 2004 Differential role for phospholipase D1 and phospholipase D2 in 12-O-tetradecanoyl-13-phorbol acetate-stimulated MAPK activation, Cox-2 and IL-8 expression. 12-o-tetradecanoyl-13-phorbol acetate 63-100 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 15028114-0 2004 Inhibition of gastric H,K-ATPase activity and gastric epithelial cell IL-8 secretion by the pyrrolizine derivative ML 3000. 6,7-diphenyl-2,3-dihydro-1H-pyrrolizine 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 14768058-6 2004 PTX-B inhibited also interleukin-8 secretion and virus expression stimulated in chronically infected U1 promonocytic cells by intra- and/or extracellular Tat. pumiliotoxin B 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 14698135-13 2004 In the every 3-week paclitaxel group, increase in IL-8 level correlated positively with flu-like symptom (p=0.008). Paclitaxel 20-30 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 14769732-9 2004 Improvements in induced-sputum interleukin-8 (p = 0.03) and FEV(1) (p = 0.04) were observed at day 14 and day 30, respectively, in the group receiving tgAAVCF when compared to those receiving placebo. tgaavcf 151-158 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 12738686-0 2004 Low molecular weight hyaluronan from stretched lung enhances interleukin-8 expression. Hyaluronic Acid 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 14634065-3 2004 Although these are detectable even without stimulation, immunoglobulin (Ig)E receptor cross-linking is able to enhance only TNF-alpha production, but phorbol 12-myristate 13-acetate additionally promotes IL-1beta and IL-8. Tetradecanoylphorbol Acetate 150-181 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 14966737-4 2004 The aim of this study has been to determine if melatonin would lower interleukin (IL)-6, IL-8, tumor necrosis factor alpha (TNF-alpha) and nitrite/nitrate (NOx) levels and modify serum inflammation parameters, improving the clinical course of surgical neonates. Melatonin 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 14966737-12 2004 In group 1a the immediate postoperative values of cytokines were significantly higher than group 1b and group 2, but a significant improvement was observed after administration of melatonin with significantly lower levels of IL-6 and IL-8 with respect to group 2. Melatonin 180-189 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 14693163-4 2004 Glucan induced the highest level of IL-1beta mRNA and protein release after 3 h. IL-8 was induced at 3 h after glucan, but not after LPS, induction, which indicates different induction pathways. Glucans 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 14693163-4 2004 Glucan induced the highest level of IL-1beta mRNA and protein release after 3 h. IL-8 was induced at 3 h after glucan, but not after LPS, induction, which indicates different induction pathways. Glucans 111-117 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 12909591-0 2004 Differential roles for NF-kappa B in endotoxin and oxygen induction of interleukin-8 in the macrophage. Oxygen 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 15203565-2 2004 In this study, our experiments were designed to determine the role of the transcription factor nuclear factor-kappaB (NF-kappaB) and intracellular calcium in the production of interleukin (IL)-8, a main chemotactic factor, by human-derived monocytic cell line U937 and by a human epithelial HEp-2 cell line infected with M. bovis BCG. Calcium 147-154 C-X-C motif chemokine ligand 8 Homo sapiens 176-194 15203565-7 2004 When calcium influx was suppressed in M. bovis-infected cell lines, IL-8 secretion was inhibited. Calcium 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 15203565-8 2004 Notably, specific inhibitors of NF-kappaB (sulfasalazine and curcumin) inhibited M. bovis-induced IL-8 secretion from U937 cells or HEp-2 cells. Sulfasalazine 43-56 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 15203565-8 2004 Notably, specific inhibitors of NF-kappaB (sulfasalazine and curcumin) inhibited M. bovis-induced IL-8 secretion from U937 cells or HEp-2 cells. Curcumin 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 15203565-10 2004 Furthermore, the results showed that calcium influx had a direct effect on IL-8 secretion in U937 cells or HEp-2 cells infected with M. bovis. Calcium 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 14663153-7 2004 With HFOV, IL-8 gene expression was highly reduced in alveolar macrophages: 10 +/- 3.4 copies IL-8 mRNA/copy HPRT mRNA versus 356 +/- 142; p < 0.05 (bronchiolar epithelial cells: 33 +/- 16 versus 208 +/- 108; alveolar septum: 2.1 +/- 1.3 versus 26 +/- 11; bronchiolar smooth muscle cells: 1.3 +/- 0.3 versus 2.8 +/- 1.0; vascular smooth muscle cells: 0.7 +/- 0.3 versus 1.1 +/- 0.4). hfov 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 14663153-7 2004 With HFOV, IL-8 gene expression was highly reduced in alveolar macrophages: 10 +/- 3.4 copies IL-8 mRNA/copy HPRT mRNA versus 356 +/- 142; p < 0.05 (bronchiolar epithelial cells: 33 +/- 16 versus 208 +/- 108; alveolar septum: 2.1 +/- 1.3 versus 26 +/- 11; bronchiolar smooth muscle cells: 1.3 +/- 0.3 versus 2.8 +/- 1.0; vascular smooth muscle cells: 0.7 +/- 0.3 versus 1.1 +/- 0.4). hfov 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 14738568-8 2004 RESULTS: We found that glutamine deprivation and treatment with a chemical inducer of ER stress (tunicamycin) caused a marked induction of the secretion of both VEGF and IL-8 protein by a human breast adenocarcinoma cell line (TSE cells). Glutamine 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 14738568-8 2004 RESULTS: We found that glutamine deprivation and treatment with a chemical inducer of ER stress (tunicamycin) caused a marked induction of the secretion of both VEGF and IL-8 protein by a human breast adenocarcinoma cell line (TSE cells). Tunicamycin 97-108 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 14738568-9 2004 Glutamine deprivation, glucose deprivation and several chemical inducers of ER stress increased VEGF and IL-8 mRNA expression in TSE and other breast cancer cell lines cultured under both normoxic and hypoxic conditions, though hypoxia generally diminished the effects of glucose deprivation. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 14738568-10 2004 Of all amino acids tested, ambient glutamine availability had the largest effect on VEGF and IL-8 mRNA expression. Glutamine 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 14527339-2 2004 By immunoprecipitation using an anti-syndecan-2 antibody on TNF-alpha-stimulated HUVEC lysates, inflammation-induced interleukin-8 was found to be an interaction partner of this HS (heparan sulphate) proteoglycan, but not of any other syndecan on these cells. Heparitin Sulfate 182-198 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 14705951-5 2004 Naloxone induced peripheral blood nonadherent mononuclear cell and neutrophil chemotaxis at nanomolar concentrations and deactivated their migration toward beta-endorphin, angiotensin II, somatostatin, or interleukin-8 but not toward RANTES, vasoactive intestinal peptide, or substance P. Naloxone 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 205-218 12948934-4 2004 In response to hrHRF, these cells induced IL-8 mRNA expression within 4 h. H2O2, but not IL-1 beta or tumor necrosis factor-alpha, stimulated secretion of HRF p23 by BEAS-2B cells, suggesting that oxidative stress may trigger the release of HRF p23 from bronchial epithelial cells. Hydrogen Peroxide 75-79 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 13129857-6 2004 Dexamethasone (50 nM) attenuated IL-8 production by 50% (P < 0.05), and IL-1beta (2 microg/l) increased IL-8 production up to 15-fold (P < 0.001). Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 15630185-0 2004 Regulation of interleukin-8 secretion in human intestinal epithelial Caco-2 cells by alpha-humulene. humulene 85-99 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 14706599-9 2004 RESULTS: Heparin concentrations > or =20 IU/mL significantly increased LPS-induced IL-8 production. Heparin 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 15630234-8 2004 The H2O2 induced increase in IL-8 secretion was inhibited by a pretreatment with carnosine for 3 h, this inhibition being presented in a dose-dependent manner. Hydrogen Peroxide 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 15630185-4 2004 Among the compounds known to be contained in peppermint and dokudami, alpha-humulene substantially increased the IL-8 secretion.alpha-Humulene had no significant effect on the secretion of such other soluble factors as TNF-alpha, IL-1beta, IL-6, or NGF, suggesting that the effect of alpha-humulene was specific for IL-8 secretion. humulene 70-84 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 15630185-5 2004 The expression level of IL-8 mRNA was significantly increased by treating with alpha-humulene. humulene 79-93 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 15630185-6 2004 These results suggest that the secretion of IL-8 by alpha-humulene is regulated at the transcriptional level. humulene 52-66 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 15273781-0 2004 Effect of 0.02% NaF solution on enamel demineralization and fluoride uptake by deciduous teeth in vitro. Fluorides 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 15273781-3 2004 The treatment with fluoride dentifrice was more effective in reducing enamel demineralization (p < 0.05) and on fluoride uptake by the enamel (p < 0.05) than the non-fluoride dentifrice and the 0.02% NaF solution. Fluorides 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 206-209 14718443-13 2004 G-CSF in serum and IL-8 in BALF correlated negatively with PaO(2)/fraction of inspired oxygen (FIO(2)) ratio. Oxygen 87-93 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 14684972-5 2004 Two hours after brushing with fluoride toothpaste containing AmF and NaF, the salivary fluoride levels were still higher than baseline levels. Fluorides 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 14684972-5 2004 Two hours after brushing with fluoride toothpaste containing AmF and NaF, the salivary fluoride levels were still higher than baseline levels. Fluorides 87-95 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 15005008-0 2004 Effects of physiological concentrations of steroid hormones and interleukin-11 on basal and stimulated production of interleukin-8 by human osteoblast-like cells with different functional profiles. Steroids 43-59 C-X-C motif chemokine ligand 8 Homo sapiens 117-130 15005008-7 2004 RESULTS: Cortisol dose-dependently inhibited spontaneous IL-8 secretion in both cell lines, although statistical significance was attained in the MG-63 cells only (P < 0.01); no effect of 17 beta-estradiol was apparent. Hydrocortisone 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 15005008-4 2004 The aim of the present study was to evaluate the single and combined effects of physiological concentrations of cortisol, 17 beta-estradiol and IL-11 upon basal and IL-1 beta-inducible production of IL-8 in two human osteoblast-like cell lines, Saos-2 and MG-63. Hydrocortisone 112-120 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 15005008-8 2004 With regard to IL-1 beta-inducible production, cortisol dose-dependently inhibited IL-8 release in both cell lines (P < 0.01); 17 beta-estradiol resulted in only a non-significant decrease in Saos-2, but not in MG-63 cells. Hydrocortisone 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 15005008-4 2004 The aim of the present study was to evaluate the single and combined effects of physiological concentrations of cortisol, 17 beta-estradiol and IL-11 upon basal and IL-1 beta-inducible production of IL-8 in two human osteoblast-like cell lines, Saos-2 and MG-63. Estradiol 122-139 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 14967603-6 2004 Both IL-8 and RANTES were significantly released by 48 hours following inoculation with RSV. Respiratory Syncytial Virus Vaccines 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 14741067-0 2004 Effect of interleukin 8 and ICAM-1 on calcium-dependent outflow of K+ in erythrocytes from subjects with essential hypertension. Calcium 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 10-23 14740733-4 2004 During reaction of metaschoepite in NaNO3, CsNO3, and NaF solutions, an initial increase in the dissolved uranium concentration was followed by a decrease as uranium was incorporated into a secondary solid phase. Uranium 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 14740733-4 2004 During reaction of metaschoepite in NaNO3, CsNO3, and NaF solutions, an initial increase in the dissolved uranium concentration was followed by a decrease as uranium was incorporated into a secondary solid phase. Uranium 158-165 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 14967603-9 2004 The authors conclude that, in differentiated human airway epithelium in vitro, RSV-induced increases in IL-8 and RANTES release are predominantly in the basolateral direction. Respiratory Syncytial Virus Vaccines 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 14734137-0 2004 N-acetylcysteine inhibits interleukin-17-induced interleukin-8 production from human airway smooth muscle cells: a possible role for anti-oxidative treatment in chronic lung rejection? Acetylcysteine 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 15568616-8 2004 This additive effect on IL-8 release was reduced when the cells were also treated with PD-098059, a selective inhibitor of the MEK1 activator and the MAPK cascade, or SB203580, a specific inhibitor of the p38 pathway, or AG490, a specific JAK/STAT pathway inhibitor, providing evidence that there are different signal pathways activated which have a cumulative effect. SB 203580 167-175 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 15349826-7 2004 On the basis of the consensus sequence glutamic acid-leucine-arginine (ELR) preceding the canonical cysteine-any amino acid-cysteine (CXC), ELR-positive CXC chemokines, such as interleukin-8 and granulocyte chemotactic protein-2, are angiogenic and thus instruct the host to feed the tumor and bring the vessels into closer contact with the tumor cells. elr 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 177-190 15349826-7 2004 On the basis of the consensus sequence glutamic acid-leucine-arginine (ELR) preceding the canonical cysteine-any amino acid-cysteine (CXC), ELR-positive CXC chemokines, such as interleukin-8 and granulocyte chemotactic protein-2, are angiogenic and thus instruct the host to feed the tumor and bring the vessels into closer contact with the tumor cells. amino acid-cysteine 113-132 C-X-C motif chemokine ligand 8 Homo sapiens 177-190 14730209-11 2004 The specific tyrosine kinase inhibitor, genistein, and the protein kinase C (PKC) inhibitor, Ro 31-8220, also inhibited IL-8 release and mRNA expression as well as p38 and NF-kappaB activation. Genistein 40-49 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 14734137-9 2004 CONCLUSIONS: We demonstrated that human airway smooth muscle cells, when stimulated with IL-17, are able to produce 8-isoprostane, which could be inhibited by adding N-acetylcysteline, and which was also able to decrease IL-17-induced IL-8 production. 8-epi-prostaglandin F2alpha 116-129 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 14734137-9 2004 CONCLUSIONS: We demonstrated that human airway smooth muscle cells, when stimulated with IL-17, are able to produce 8-isoprostane, which could be inhibited by adding N-acetylcysteline, and which was also able to decrease IL-17-induced IL-8 production. n-acetylcysteline 166-183 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 14661260-2 2004 It was found that the fracture of titanium occurred in neutral 2.0% NaF solution as well as in 2.0% acidulated phosphate fluoride (APF) solution. Titanium 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 15509017-9 2004 We report here on the potency of nano-metal particles with single or binary chemical components in eliciting interleukin-8 (IL-8) production from epithelial cell lines. Metals 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 109-122 15509017-9 2004 We report here on the potency of nano-metal particles with single or binary chemical components in eliciting interleukin-8 (IL-8) production from epithelial cell lines. Metals 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 15509017-10 2004 For single-component nanoparticles, we found that nano-Cu particles were more potent in IL-8 production than nano-Ni and nano-V particles. Copper 55-57 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 15509017-12 2004 When sulfuric acid was introduced to form acidified nano-Ni particles, we found that the potency of such binary-component nanoparticles in eliciting IL-8 production was increased markedly, by about six times. sulfuric acid 5-18 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 15509017-14 2004 Since Ni, a transition metal, could induce free radicals on cell surfaces, while Na and Mg could not, the acidity might have enhanced the oxidative stress caused by radicals to the cells, leading to markedly higher IL-8 production. Free Radicals 43-56 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 14734137-8 2004 N-acetylcysteine (NAC) was able to decrease IL-17-induced 8-isoprostane production, with a maximum decrease of 59.3 +/- 9% (p < 0.001, n = 12) with 10 mmol/liter of N-acetylcysteine, which also decreased IL-17-induced IL-8 production in a concentration-dependent manner (with maximum inhibition of 86.3% when combined with NAC 10 mmol/liter as compared with IL-17 alone). Acetylcysteine 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 14734137-8 2004 N-acetylcysteine (NAC) was able to decrease IL-17-induced 8-isoprostane production, with a maximum decrease of 59.3 +/- 9% (p < 0.001, n = 12) with 10 mmol/liter of N-acetylcysteine, which also decreased IL-17-induced IL-8 production in a concentration-dependent manner (with maximum inhibition of 86.3% when combined with NAC 10 mmol/liter as compared with IL-17 alone). Acetylcysteine 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 14756775-7 2004 In addition, recombinant N-pmpD activated human monocytes in vitro by upregulating their metabolic activity and by stimulating IL-8 release in a dose-dependent manner. n-pmpd 25-31 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 14688319-6 2004 Furthermore, NK cells respond to poly(I:C) by producing proinflammatory cytokines like IL-6 and IL-8, as well as the antiviral cytokine IFN-gamma. poly 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 14688319-6 2004 Furthermore, NK cells respond to poly(I:C) by producing proinflammatory cytokines like IL-6 and IL-8, as well as the antiviral cytokine IFN-gamma. Iodine 38-39 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 14688319-6 2004 Furthermore, NK cells respond to poly(I:C) by producing proinflammatory cytokines like IL-6 and IL-8, as well as the antiviral cytokine IFN-gamma. Carbon 40-41 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 15082095-3 2004 This should result in passive attachment (stem cells to tagged tissue or organ); and (3) Reticulose, which stimulates the synthesis of the stem cell chemoattractant IL-8, could be magnetically guided to target tissue(s) and/or organ(s). reticulose 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 15046557-5 2004 Conversely, TNF-alpha, IL-6, and IL-8 increased reactive oxygen species production and the expression of CD11b and CD15 on both neutrophils and monocytes and decreased the expression of CD62L. Reactive Oxygen Species 48-71 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 15165037-6 2004 The presence of NaF in the assay mixture resulted to a decreased degradation of alkylacetylphosphatidic acid, as well as to an increased overall product formation. alkylacetylphosphatidic acid 80-108 C-X-C motif chemokine ligand 8 Homo sapiens 16-19 14979662-5 2004 PDGF-AB, TGF-beta1 and IL-8 provoke conformational changes in mollusk immunocytes, involving the signaling transduction pathways of phosphatidylinositol and cAMP. Phosphatidylinositols 132-152 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 14979662-5 2004 PDGF-AB, TGF-beta1 and IL-8 provoke conformational changes in mollusk immunocytes, involving the signaling transduction pathways of phosphatidylinositol and cAMP. Cyclic AMP 157-161 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 15230146-8 2004 Furthermore TNF-alpha and IL-8 levels correlated with pleocytosis, and protein and glucose levels, whereas IL-1 beta correlated with pleocytosis and protein level in CSF. Glucose 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 14643170-5 2004 Pre-treatment with beclomethasone, budesonide or fluticasone reduced TNFalpha- and IL-1beta-stimulated IL-8 and RANTES release from HASMC in a dose dependent manner. Beclomethasone 19-33 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 14643170-5 2004 Pre-treatment with beclomethasone, budesonide or fluticasone reduced TNFalpha- and IL-1beta-stimulated IL-8 and RANTES release from HASMC in a dose dependent manner. Budesonide 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 14643170-5 2004 Pre-treatment with beclomethasone, budesonide or fluticasone reduced TNFalpha- and IL-1beta-stimulated IL-8 and RANTES release from HASMC in a dose dependent manner. Fluticasone 49-60 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 14643170-7 2004 TNFalpha- and IL-1beta-induced RANTES and IL-8 expression was reduced on the transcriptional level by pre-treatment with fluticasone and budesonide. Fluticasone 121-132 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 14643170-7 2004 TNFalpha- and IL-1beta-induced RANTES and IL-8 expression was reduced on the transcriptional level by pre-treatment with fluticasone and budesonide. Budesonide 137-147 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 14643170-8 2004 The results suggest that the topical steroids fluticasone, budesonide and to a lesser extent beclomethasone may have beneficial effects on airway inflammation in asthma by reducing RANTES and IL-8-induced leukocyte infiltration into the airway wall. Steroids 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 14643170-2 2004 This study was performed to investigate the effectiveness of the commonly used steroids beclomethasone, budesonide and fluticasone in downregulating HASMC production of RANTES and IL-8. Steroids 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 14643170-2 2004 This study was performed to investigate the effectiveness of the commonly used steroids beclomethasone, budesonide and fluticasone in downregulating HASMC production of RANTES and IL-8. Beclomethasone 88-102 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 14643170-2 2004 This study was performed to investigate the effectiveness of the commonly used steroids beclomethasone, budesonide and fluticasone in downregulating HASMC production of RANTES and IL-8. Budesonide 104-114 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 14643170-2 2004 This study was performed to investigate the effectiveness of the commonly used steroids beclomethasone, budesonide and fluticasone in downregulating HASMC production of RANTES and IL-8. Fluticasone 119-130 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 14643170-2 2004 This study was performed to investigate the effectiveness of the commonly used steroids beclomethasone, budesonide and fluticasone in downregulating HASMC production of RANTES and IL-8. hasmc 149-154 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 14643170-8 2004 The results suggest that the topical steroids fluticasone, budesonide and to a lesser extent beclomethasone may have beneficial effects on airway inflammation in asthma by reducing RANTES and IL-8-induced leukocyte infiltration into the airway wall. Fluticasone 46-57 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 14643170-8 2004 The results suggest that the topical steroids fluticasone, budesonide and to a lesser extent beclomethasone may have beneficial effects on airway inflammation in asthma by reducing RANTES and IL-8-induced leukocyte infiltration into the airway wall. Budesonide 59-69 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 14643170-8 2004 The results suggest that the topical steroids fluticasone, budesonide and to a lesser extent beclomethasone may have beneficial effects on airway inflammation in asthma by reducing RANTES and IL-8-induced leukocyte infiltration into the airway wall. Beclomethasone 93-107 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 20021137-12 2004 Replacement of NaCl with LiCl decreased the L-cysteine uptake by about 5-fold and in the presence of NaF decrease in L-cysteine uptake was about 2 fold. Sodium Chloride 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 16295318-9 2004 The results demonstrate an important oxidative aggression induced by three sources: the alcohol metabolism in the hepatocytes, activated Kupffer cells and activated neutrophils that have infiltrated the liver, due to the chemoattractant effect of IL-8. Alcohols 88-95 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 15081568-0 2004 The effect of TNF-alpha, PMA, and LPS on plasma and cell-associated IL-8 in human leukocytes. Tetradecanoylphorbol Acetate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 15108454-7 2004 A negative correlation was discovered between IL-1 beta, TNF alpha and body mass index; IL-8 and osteocalcine. osteocalcine 97-109 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 20021137-12 2004 Replacement of NaCl with LiCl decreased the L-cysteine uptake by about 5-fold and in the presence of NaF decrease in L-cysteine uptake was about 2 fold. Cysteine 117-127 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 15606218-8 2004 The combination of corticosteroids and LABA potentiates inhibition of interleukin-8 and eotaxin release from human airway smooth muscle cells and granulocyte-macrophage colony-stimulating factor release from epithelial cells, and also the inhibition of airway smooth muscle cell proliferation. LABA 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 14719805-0 2003 Semisynthesis and application of carboxyfluorescein-labelled biologically active human interleukin-8. 6-carboxyfluorescein 33-51 C-X-C motif chemokine ligand 8 Homo sapiens 87-100 14615068-6 2003 As results, retinoid-induced inflammation was mainly mediated through MCP-1 and IL-8 as evidenced by increased levels of mRNA expression and protein secretion. Retinoids 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 14615068-10 2003 In conclusion, the present study demonstrated that among proinflammatory cytokines, MCP-1 and IL-8 mainly mediated retinol-induced skin irritation, and that inhibition of production of these cytokines can be applied as good markers to screen the anti-irritants against the retinol-induced irritation. Vitamin A 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 14615068-10 2003 In conclusion, the present study demonstrated that among proinflammatory cytokines, MCP-1 and IL-8 mainly mediated retinol-induced skin irritation, and that inhibition of production of these cytokines can be applied as good markers to screen the anti-irritants against the retinol-induced irritation. Vitamin A 273-280 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 16465705-5 2003 The diffusion coefficients of cobalt(II) tris(bipyridine), ferrocenemethyltrimethylammonium ion, and dicyanobis(phenanthroline)iron(II) and their rate of change as the gel dried were found to be nearly identical for gels prepared from TMOS and catalyzed with either HCl, NH3, or NaF. cobalt(ii) tris 30-45 C-X-C motif chemokine ligand 8 Homo sapiens 279-282 14719805-4 2003 The ligation site was chosen with respect to the position of four cysteine residues within the hIL-8 sequence. Cysteine 66-74 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 14719805-5 2003 Ligation with synthetic peptides that carry cysteine at their N-termini resulted in full-length hIL-8 and the specifically carboxyfluorescein-labelled analogue [K69(CF)]hIL-8(1-77). Cysteine 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 96-101 14719805-5 2003 Ligation with synthetic peptides that carry cysteine at their N-termini resulted in full-length hIL-8 and the specifically carboxyfluorescein-labelled analogue [K69(CF)]hIL-8(1-77). Cysteine 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 169-174 14719805-5 2003 Ligation with synthetic peptides that carry cysteine at their N-termini resulted in full-length hIL-8 and the specifically carboxyfluorescein-labelled analogue [K69(CF)]hIL-8(1-77). 6-carboxyfluorescein 123-141 C-X-C motif chemokine ligand 8 Homo sapiens 169-174 14719805-6 2003 [K69(CF)]hIL-8(1-77) was fully active as shown by inhibition of cAMP production. Cyclic AMP 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 9-14 14636727-11 2003 The extent of STT was correlated best to IL-8 (r=0.75), IL-6 (r=0.54), and creatine kinase (CK, r=0.49) plasma concentrations. SCHEMBL22553698 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 14613754-0 2003 Linoleic acid, but not oleic acid, upregulates the production of interleukin-8 by human intestinal smooth muscle cells isolated from patients with Crohn"s disease. Linoleic Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 14613754-0 2003 Linoleic acid, but not oleic acid, upregulates the production of interleukin-8 by human intestinal smooth muscle cells isolated from patients with Crohn"s disease. Oleic Acid 3-13 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 14613754-2 2003 In this study, we investigated the hypothesis that dietary fatty acids, linoleic acid (LA) and oleic acid (OA), could be involved in the inflammatory response through stimulation of the neutrophil chemokine, IL-8. dietary fatty acids 51-70 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 14613754-2 2003 In this study, we investigated the hypothesis that dietary fatty acids, linoleic acid (LA) and oleic acid (OA), could be involved in the inflammatory response through stimulation of the neutrophil chemokine, IL-8. Linoleic Acid 72-85 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 14613754-2 2003 In this study, we investigated the hypothesis that dietary fatty acids, linoleic acid (LA) and oleic acid (OA), could be involved in the inflammatory response through stimulation of the neutrophil chemokine, IL-8. Oleic Acid 75-85 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 14613754-2 2003 In this study, we investigated the hypothesis that dietary fatty acids, linoleic acid (LA) and oleic acid (OA), could be involved in the inflammatory response through stimulation of the neutrophil chemokine, IL-8. Oleic Acid 107-109 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 14636828-3 2003 Treatment of neutrophils with MCD caused inhibition of intracellular calcium increase evoked by interleukin-8 (IL-8) or low concentrations of formyl-Met-Leu-Phe (fMLP). methyl-beta-cyclodextrin 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 14575864-3 2003 Stimulation of IL-8 expression was completely attenuated by two inhibitors of mitogen-activated protein kinase (MAPK) kinase (MEK), which phosphorylates the MAPKs extracellular-regulated kinase (ERK)1 and ERK2, and by the c-Jun NH2-terminal kinase (JNK) inhibitor SP600125. pyrazolanthrone 264-272 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 12876073-8 2003 AT mRNA of TNF-alpha, IL-6, and IL-8 was increased in AT of HALS subjects (P < 0.05), and both AT TNF-alpha mRNA and plasma TNF-alpha were negatively correlated to plasma adiponectin (P < 0.05). Fluoxymesterone 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 14676436-0 2003 Exposure to toluene diisocyanate (TDI) induces IL-8 production from bronchial epithelial cells: effect of pro-inflammatory cytokines. Toluene 2,4-Diisocyanate 12-32 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 14676436-0 2003 Exposure to toluene diisocyanate (TDI) induces IL-8 production from bronchial epithelial cells: effect of pro-inflammatory cytokines. Toluene 2,4-Diisocyanate 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 14676436-1 2003 This investigation was designed to confirm IL-8 production from human bronchial epithelial cells with toluene diisocyanate (TDI) exposure and to examine the effects of pro-inflammatory cytokine and dexamethasone. Toluene 2,4-Diisocyanate 102-122 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 14676436-1 2003 This investigation was designed to confirm IL-8 production from human bronchial epithelial cells with toluene diisocyanate (TDI) exposure and to examine the effects of pro-inflammatory cytokine and dexamethasone. Toluene 2,4-Diisocyanate 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 14676436-6 2003 There was a significant production of IL-8 from bronchial epithelial cells with addition of TDI-HSA conjugate in a dose-dependent manner, which was significantly augmented with addition of PBMC supernatant. tdi-hsa 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 14676436-9 2003 Pre-treatment of dexamethasone induced dose-dependent inhibition of the IL-8 production. Dexamethasone 17-30 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 14725359-1 2003 PURPOSE: The aim of the study was to investigate the effect of histidine on the stability and physical properties of a fully human anti-IL8 monoclonal antibody (ABX-IL8) in aqueous and solid forms. Histidine 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 14725359-1 2003 PURPOSE: The aim of the study was to investigate the effect of histidine on the stability and physical properties of a fully human anti-IL8 monoclonal antibody (ABX-IL8) in aqueous and solid forms. Histidine 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 165-168 14725359-1 2003 PURPOSE: The aim of the study was to investigate the effect of histidine on the stability and physical properties of a fully human anti-IL8 monoclonal antibody (ABX-IL8) in aqueous and solid forms. CHEMBL369125 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 14725359-1 2003 PURPOSE: The aim of the study was to investigate the effect of histidine on the stability and physical properties of a fully human anti-IL8 monoclonal antibody (ABX-IL8) in aqueous and solid forms. CHEMBL369125 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 165-168 14725359-11 2003 CONCLUSIONS: Histidine enhanced the stability of ABX-IL8 in both aqueous and lyophilized forms. Histidine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 14615040-2 2003 We have previously shown that Fas ligation induces expression of chemokines such as interleukin-8 by human astrogliomas, which may partially explain the in vivo angiogenic property of FasL. ammonium ferrous sulfate 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 12812920-5 2003 However, zinc deficiency increased the levels of TNF-alpha, IL-1 beta, and IL-8 cytokines and mRNAs in HL-60 cells after 6 h of PMA stimulation compared with zinc-sufficient cells. Tetradecanoylphorbol Acetate 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 12876073-0 2003 Increased expression of TNF-alpha, IL-6, and IL-8 in HALS: implications for reduced adiponectin expression and plasma levels. Fluoxymesterone 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 14636828-3 2003 Treatment of neutrophils with MCD caused inhibition of intracellular calcium increase evoked by interleukin-8 (IL-8) or low concentrations of formyl-Met-Leu-Phe (fMLP). methyl-beta-cyclodextrin 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 14636828-3 2003 Treatment of neutrophils with MCD caused inhibition of intracellular calcium increase evoked by interleukin-8 (IL-8) or low concentrations of formyl-Met-Leu-Phe (fMLP). Calcium 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 14636828-3 2003 Treatment of neutrophils with MCD caused inhibition of intracellular calcium increase evoked by interleukin-8 (IL-8) or low concentrations of formyl-Met-Leu-Phe (fMLP). Calcium 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 14636828-8 2003 Cholesterol depletion greatly inhibited IL-8-induced elastase release but had little effect of fMLP-induced degranulation. Cholesterol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 14676436-10 2003 These results suggest that the IL-8 production from bronchial epithelial cells contribute to neutrophil recruitment occurring in TDI-induced airway inflammation. Toluene 2,4-Diisocyanate 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 14599546-3 2003 5-FU increased interleukin-8 production and induced morphological signs of irritation. Fluorouracil 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 12842821-5 2003 However, iron/ascorbate-mediated lipid peroxidation promoted inhibitor-kappaB degradation and NF-kappaB activation, as well as gave rise to IL-8, cyclooxygenase-2, and ICAM-1. Iron 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 12842821-5 2003 However, iron/ascorbate-mediated lipid peroxidation promoted inhibitor-kappaB degradation and NF-kappaB activation, as well as gave rise to IL-8, cyclooxygenase-2, and ICAM-1. Ascorbic Acid 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 14499342-5 2003 Lipopolysaccharide (LPS)-induced IL-8 production was inhibited by SB203580, but not by the MK2 inhibitory peptide. SB 203580 66-74 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 12958044-4 2003 We thus investigated whether synthesis of IL-8 from primary human aortic smooth muscle cells is influenced by CsA and FK506. Tacrolimus 118-123 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 14981920-1 2003 We have recently found that sodium fluoride (NaF) induced apoptotic cell death in tumor cell lines. Sodium Fluoride 28-43 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 14981920-7 2003 NaF reduced the glucose consumption at early stage, possibly by inhibition of glycolysis, whereas cisplatin and etoposide reduced the glucose consumption at later stage, suggesting that early decline of glucose consumption is rather specific to NaF. Glucose 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 14981920-7 2003 NaF reduced the glucose consumption at early stage, possibly by inhibition of glycolysis, whereas cisplatin and etoposide reduced the glucose consumption at later stage, suggesting that early decline of glucose consumption is rather specific to NaF. Cisplatin 98-107 C-X-C motif chemokine ligand 8 Homo sapiens 245-248 14981920-7 2003 NaF reduced the glucose consumption at early stage, possibly by inhibition of glycolysis, whereas cisplatin and etoposide reduced the glucose consumption at later stage, suggesting that early decline of glucose consumption is rather specific to NaF. Etoposide 112-121 C-X-C motif chemokine ligand 8 Homo sapiens 245-248 12908082-0 2003 Induction of TNF-alpha, uPA, IL-8 and MCP-1 by doxorubicin in human lung carcinoma cells. Doxorubicin 47-58 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 12908082-1 2003 PURPOSE: We have previously demonstrated doxorubicin-induced urokinase (uPA) and interleukin-8 (IL-8) expression in human H69 small-cell lung carcinoma (SCLC) cells by a microarray technique using Human Cancer Chip version 2, in which 425 human "cancer-related" genes are spotted on the plates. Doxorubicin 41-52 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 12908082-1 2003 PURPOSE: We have previously demonstrated doxorubicin-induced urokinase (uPA) and interleukin-8 (IL-8) expression in human H69 small-cell lung carcinoma (SCLC) cells by a microarray technique using Human Cancer Chip version 2, in which 425 human "cancer-related" genes are spotted on the plates. Doxorubicin 41-52 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 14605526-12 2003 Interleukin-8 decreased significantly only in those who received N-acetylcysteine (p =.0081). Acetylcysteine 65-81 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 14625697-6 2003 When preincubated with enzyme, several chelators such as citrate, NaF, N-(2-hydroxyethyl) ethylenediaminetriacetic acid or ethylenediaminetriacetic acid efficiently protected the enzyme against the aluminum inactivation. Aluminum 198-206 C-X-C motif chemokine ligand 8 Homo sapiens 66-69 14625697-7 2003 In a related experiment, only citrate and NaF released the aluminum from the completely inactivated aluminum-enzyme complex and fully recovered the enzyme activity. Aluminum 59-67 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 14642127-6 2003 RESULTS: After 96 hours exposure to arsenic trioxide, 10 - 6 mol/L in vitro or 10 mg/d in vivo, APL cells showed a significant increase of IL-1(beta) (P < 0.05) and G-CSF (P < 0.05) production, and a significant decrease of IL-6 (P < 0.05) and IL-8 (P < 0.05). Arsenic Trioxide 36-52 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 14605526-14 2003 CONCLUSIONS: Administration of N-acetylcysteine results in decreased nuclear factor-kappa B activation in patients with sepsis, associated with decreases in interleukin-8 but not interleukin-6 or soluble intercellular adhesion molecule-1. Acetylcysteine 31-47 C-X-C motif chemokine ligand 8 Homo sapiens 157-170 14572605-0 2003 Selenium-containing compounds attenuate peroxynitrite-mediated NF-kappaB and AP-1 activation and interleukin-8 gene and protein expression in human leukocytes. Selenium 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 14572605-1 2003 A growing body of evidence indicates that the powerful oxidant peroxynitrite (ONOO(-)) may function as an intracellular signal for production of proinflammatory cytokines, such as interleukin-8 (IL-8) in human leukocytes. Peroxynitrous Acid 63-76 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 14572605-1 2003 A growing body of evidence indicates that the powerful oxidant peroxynitrite (ONOO(-)) may function as an intracellular signal for production of proinflammatory cytokines, such as interleukin-8 (IL-8) in human leukocytes. Peroxynitrous Acid 63-76 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 14572605-1 2003 A growing body of evidence indicates that the powerful oxidant peroxynitrite (ONOO(-)) may function as an intracellular signal for production of proinflammatory cytokines, such as interleukin-8 (IL-8) in human leukocytes. onoo(-) 78-85 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 14572605-1 2003 A growing body of evidence indicates that the powerful oxidant peroxynitrite (ONOO(-)) may function as an intracellular signal for production of proinflammatory cytokines, such as interleukin-8 (IL-8) in human leukocytes. onoo(-) 78-85 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 14572605-2 2003 In this study, we investigated whether selenomethionine, selenocysteine, and the synthetic organoselenium compound ebselen (2-phenyl-1,2-benzisoselenazol-3(2h)-one) could inhibit ONOO(-)-mediated IL-8 gene expression in human leukocytes in whole blood. ebselen 124-163 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 14572605-3 2003 At micromolar concentrations, ebselen, selenomethionine, and selenocysteine effectively prevented nuclear accumulation of activator protein-1 (AP-1) and nuclear factor kappaB (NF-kappaB) evoked by exogenous ONOO(-), in both polymorphonuclear and mononuclear leukocytes, and inhibited IL-8 gene and protein expression. ebselen 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 284-288 14572605-3 2003 At micromolar concentrations, ebselen, selenomethionine, and selenocysteine effectively prevented nuclear accumulation of activator protein-1 (AP-1) and nuclear factor kappaB (NF-kappaB) evoked by exogenous ONOO(-), in both polymorphonuclear and mononuclear leukocytes, and inhibited IL-8 gene and protein expression. Selenomethionine 39-55 C-X-C motif chemokine ligand 8 Homo sapiens 284-288 14572605-3 2003 At micromolar concentrations, ebselen, selenomethionine, and selenocysteine effectively prevented nuclear accumulation of activator protein-1 (AP-1) and nuclear factor kappaB (NF-kappaB) evoked by exogenous ONOO(-), in both polymorphonuclear and mononuclear leukocytes, and inhibited IL-8 gene and protein expression. Selenocysteine 61-75 C-X-C motif chemokine ligand 8 Homo sapiens 284-288 14671485-10 2003 In vitro studies revealed that UR-12715 or 5-ASA (from 10(-6) to 10(-4) M) inhibited IL-8 production (30-40%) in HT-29 cells when incubated with LPS. Urea 31-33 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 14572605-5 2003 Furthermore, ebselen, selenomethionine, and selenocysteine markedly reduced LPS-evoked intracellular ONOO(-) formation in leukocytes, resulting in 36-66% decreases in nuclear accumulation of AP-1 and NF-kappaB in both polymorphonuclear and mononuclear leukocytes and inhibition of IL-8 mRNA expression and IL-8 release. ebselen 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 281-285 14671485-10 2003 In vitro studies revealed that UR-12715 or 5-ASA (from 10(-6) to 10(-4) M) inhibited IL-8 production (30-40%) in HT-29 cells when incubated with LPS. 5-Aminosalicylic acid 43-48 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 14572605-5 2003 Furthermore, ebselen, selenomethionine, and selenocysteine markedly reduced LPS-evoked intracellular ONOO(-) formation in leukocytes, resulting in 36-66% decreases in nuclear accumulation of AP-1 and NF-kappaB in both polymorphonuclear and mononuclear leukocytes and inhibition of IL-8 mRNA expression and IL-8 release. ebselen 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 306-310 14572605-5 2003 Furthermore, ebselen, selenomethionine, and selenocysteine markedly reduced LPS-evoked intracellular ONOO(-) formation in leukocytes, resulting in 36-66% decreases in nuclear accumulation of AP-1 and NF-kappaB in both polymorphonuclear and mononuclear leukocytes and inhibition of IL-8 mRNA expression and IL-8 release. Selenomethionine 22-38 C-X-C motif chemokine ligand 8 Homo sapiens 281-285 14572605-5 2003 Furthermore, ebselen, selenomethionine, and selenocysteine markedly reduced LPS-evoked intracellular ONOO(-) formation in leukocytes, resulting in 36-66% decreases in nuclear accumulation of AP-1 and NF-kappaB in both polymorphonuclear and mononuclear leukocytes and inhibition of IL-8 mRNA expression and IL-8 release. Selenomethionine 22-38 C-X-C motif chemokine ligand 8 Homo sapiens 306-310 14572605-5 2003 Furthermore, ebselen, selenomethionine, and selenocysteine markedly reduced LPS-evoked intracellular ONOO(-) formation in leukocytes, resulting in 36-66% decreases in nuclear accumulation of AP-1 and NF-kappaB in both polymorphonuclear and mononuclear leukocytes and inhibition of IL-8 mRNA expression and IL-8 release. Selenocysteine 44-58 C-X-C motif chemokine ligand 8 Homo sapiens 281-285 14572605-5 2003 Furthermore, ebselen, selenomethionine, and selenocysteine markedly reduced LPS-evoked intracellular ONOO(-) formation in leukocytes, resulting in 36-66% decreases in nuclear accumulation of AP-1 and NF-kappaB in both polymorphonuclear and mononuclear leukocytes and inhibition of IL-8 mRNA expression and IL-8 release. Selenocysteine 44-58 C-X-C motif chemokine ligand 8 Homo sapiens 306-310 14666025-3 2003 This study was designed to compare the effects of epsilon-aminocaproic acid and aprotinin on plasma levels of interleukin-6 and interleukin-8 during and after cardiopulmonary bypass. Aminocaproic Acid 50-75 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 12960242-0 2003 Nicotine induces human neutrophils to produce IL-8 through the generation of peroxynitrite and subsequent activation of NF-kappaB. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 12960242-0 2003 Nicotine induces human neutrophils to produce IL-8 through the generation of peroxynitrite and subsequent activation of NF-kappaB. Peroxynitrous Acid 77-90 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 14596794-1 2003 The role of lysophosphatidylcholine (LPC) in the induction of MCP-1, IL-8 and RANTES, which are chemotactic factors to monocytes, neutrophils and lymphocytes, respectively, by human vascular endothelial cells (EC), was examined. Lysophosphatidylcholines 12-35 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 14596794-1 2003 The role of lysophosphatidylcholine (LPC) in the induction of MCP-1, IL-8 and RANTES, which are chemotactic factors to monocytes, neutrophils and lymphocytes, respectively, by human vascular endothelial cells (EC), was examined. Lysophosphatidylcholines 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 14596794-2 2003 LPC induced the expression of MCP-1 and IL-8 in a concentration- and time-dependent manner in microvascular EC (MVEC) and in large vessel EC from aorta, pulmonary artery and umbilical vein. Lysophosphatidylcholines 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 14596794-9 2003 An inhibitor of the MAPK/ERK pathway, PD98059, blocked the phosphorylation of ERK1/2 and RANTES induction by LPC, but augmented IL-8 induction. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 14596794-11 2003 Inhibition of p38 MAP kinase pathway by SB202190 also blocked LPC-induced expression of IL-8 and RANTES. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12975484-3 2003 The putative Ins(1,4,5)P3 receptor antagonist 2-aminoethoxydiphenyl borane reduced the response to CXCR2 activation by interleukin-8, as did sustained inhibition of phosphatidylinositol 4-kinase with wortmannin, suggesting the involvement of phosphoinositides in the potentiation. 2-aminoethoxydiphenylborane 46-74 C-X-C motif chemokine ligand 8 Homo sapiens 119-132 12975484-3 2003 The putative Ins(1,4,5)P3 receptor antagonist 2-aminoethoxydiphenyl borane reduced the response to CXCR2 activation by interleukin-8, as did sustained inhibition of phosphatidylinositol 4-kinase with wortmannin, suggesting the involvement of phosphoinositides in the potentiation. Wortmannin 200-210 C-X-C motif chemokine ligand 8 Homo sapiens 119-132 12975484-3 2003 The putative Ins(1,4,5)P3 receptor antagonist 2-aminoethoxydiphenyl borane reduced the response to CXCR2 activation by interleukin-8, as did sustained inhibition of phosphatidylinositol 4-kinase with wortmannin, suggesting the involvement of phosphoinositides in the potentiation. Phosphatidylinositols 242-259 C-X-C motif chemokine ligand 8 Homo sapiens 119-132 14646384-0 2003 Azelastine inhibits secretion of IL-6, TNF-alpha and IL-8 as well as NF-kappaB activation and intracellular calcium ion levels in normal human mast cells. azelastine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 14646384-3 2003 METHODS: We investigated the effect of azelastine on the secretion of IL-6, TNF-alpha and IL-8 from hCBMC, as well as its possible mechanism of action. azelastine 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 14646384-9 2003 CONCLUSION: Azelastine inhibited hCBMC secretion of IL-6, TNF-alpha and IL-8, possibly by inhibiting intracellular Ca2+ ions and NF-kappaB activation. azelastine 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 12960242-3 2003 Nicotine stimulated neutrophils to produce IL-8 in both time- and concentration-dependent manners with a 50% effective concentration of 1.89 mM. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 12960242-6 2003 The NOS inhibitor, nomega-Nitro-l-arginine methyl ester, prevented nicotine-induced IL-8 production, with an entire abrogation of DHR oxidation, IkappaB degradation, and NF-kappaB activity. NG-Nitroarginine Methyl Ester 19-55 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 12960242-6 2003 The NOS inhibitor, nomega-Nitro-l-arginine methyl ester, prevented nicotine-induced IL-8 production, with an entire abrogation of DHR oxidation, IkappaB degradation, and NF-kappaB activity. Nicotine 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 12960242-7 2003 Neutrophils spontaneously produced NO whose production was not increased, but rather decreased by nicotine stimulation, suggesting that superoxide, produced by nicotine, generates peroxynitrite by reacting with preformed NO, which enhances the NF-kappaB activity, thereby producing IL-8. Superoxides 136-146 C-X-C motif chemokine ligand 8 Homo sapiens 282-286 12960242-7 2003 Neutrophils spontaneously produced NO whose production was not increased, but rather decreased by nicotine stimulation, suggesting that superoxide, produced by nicotine, generates peroxynitrite by reacting with preformed NO, which enhances the NF-kappaB activity, thereby producing IL-8. Nicotine 160-168 C-X-C motif chemokine ligand 8 Homo sapiens 282-286 12960242-7 2003 Neutrophils spontaneously produced NO whose production was not increased, but rather decreased by nicotine stimulation, suggesting that superoxide, produced by nicotine, generates peroxynitrite by reacting with preformed NO, which enhances the NF-kappaB activity, thereby producing IL-8. Peroxynitrous Acid 180-193 C-X-C motif chemokine ligand 8 Homo sapiens 282-286 12960242-10 2003 In conclusion, nicotine stimulates neutrophil-IL-8 production via nAChR by generating peroxynitrite and subsequent NF-kappaB activation, and the IL-8 appears to contribute to leukocytosis in tobacco smokers. Nicotine 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 12960242-10 2003 In conclusion, nicotine stimulates neutrophil-IL-8 production via nAChR by generating peroxynitrite and subsequent NF-kappaB activation, and the IL-8 appears to contribute to leukocytosis in tobacco smokers. Peroxynitrous Acid 86-99 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 14666025-7 2003 RESULTS: Both epsilon-aminocaproic acid and aprotinin administration resulted in significant (P <.05) reductions in D-dimer and interleukin-8 levels compared with saline. Aminocaproic Acid 14-39 C-X-C motif chemokine ligand 8 Homo sapiens 131-144 14666025-10 2003 CONCLUSIONS: When dosed in a similar manner, epsilon-aminocaproic acid seems to be as effective as aprotinin at reducing interleukin-6 and interleukin-8 levels in patients undergoing primary coronary artery bypass graft surgery. Aminocaproic Acid 45-70 C-X-C motif chemokine ligand 8 Homo sapiens 139-152 14600463-1 2003 HYPOTHESIS: This study investigates the function of the diastrophic dysplasia sulfate transporter (DTDST) in otosclerotic bone and the effect on it of sodium fluoride (NaF). Sodium Fluoride 151-166 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 14600463-10 2003 NaF (10(-6)M, 1 hr) inhibited sulfate uptake by the otosclerotic stapes and EAC cells but not by control samples. Sulfates 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 14600463-5 2003 Sulfate uptake was quantified under basal conditions and with NaF. Sulfates 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 14600463-6 2003 The NaF signaling pathways were investigated using forskolin and verapamil. Colforsin 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 14600463-6 2003 The NaF signaling pathways were investigated using forskolin and verapamil. Verapamil 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 14586044-8 2003 RESULTS: Resveratrol inhibited basal release of IL-8 in smokers and patients with COPD by 94% and 88% respectively, and inhibited GM-CSF release by 79% and 76% respectively. Resveratrol 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 14586044-11 2003 In addition, resveratrol inhibited CSM stimulated IL-8 release by 61% and 51% respectively in smokers and COPD patients, and inhibited GM-CSF release by 49% for both subject groups. Resveratrol 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 14595591-6 2003 In addition, peyote extract induced up to 1.85-, 2.29- and 1.89-fold increases in mRNA signal of IL-1, IL-6 and IL-8 by human leukocytes. Mescaline 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 14586044-10 2003 Resveratrol reduced IL-1beta stimulated IL-8 and GM-CSF release in both smokers and COPD patients to below basal levels. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 14728888-0 2003 [Interleukin-8 gene expression before and after the pulse treatment with methylprednisolone in primary nephrotic syndrome of children]. Methylprednisolone 73-91 C-X-C motif chemokine ligand 8 Homo sapiens 1-14 14728888-3 2003 The purpose of the study was to evaluate the serum concentration and mRNA expression of IL-8 before and after the methylprednisolone pulse therapy (MPT) in PNS. Methylprednisolone 114-132 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 14728888-21 2003 Methylprednisolone pulse therapy in PNS was able to inhibit the protein production and PBMC mRNA expression of IL-8, so the therapeutic mechanism of MPT in PNS might be associated with the inhibition of IL-8 expression. Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 14728888-21 2003 Methylprednisolone pulse therapy in PNS was able to inhibit the protein production and PBMC mRNA expression of IL-8, so the therapeutic mechanism of MPT in PNS might be associated with the inhibition of IL-8 expression. Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 14559242-6 2003 Telithromycin selectively inhibited the IL-6 and IL-8 production from Stx-stimulated (but not LPS-stimulated) monocytes. telithromycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 14556981-4 2003 Fluticasone propionate, at the two concentrations tested (10 and 100 nM), was more effective in inhibiting the "IL-4 plus TNF-alpha-induced" ICAM-1 expression than VCAM-1 expression (P<0.05) and in downregulating RANTES than IL-8 or GM-CSF secretion (P<0.05). Fluticasone 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 228-232 14550286-3 2003 Glucose (up to 35mM) increased secretion of PAI-1 (p<0.01) and IL-8 (p<0.01), but not TNF-alpha, in a dose- and time-dependent manner. Glucose 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 14550286-5 2003 Glucosamine (5mM) decreased production of PAI-1 (p<0.05) and IL-8 (p<0.05), indicating that the hexosamine biosynthesis pathway is not involved in the glucose-induced increment in adipokine secretion. Glucosamine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 14550286-6 2003 The present data demonstrate that glucose increases PAI-1 and IL-8 secretion. Glucose 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 13679236-7 2003 Moxifloxacin inhibited the release of TNFalpha, IL-1, IL-6, and IL-8 in a concentration-dependent manner across a range of 0.004 to 4 microg/mL. Moxifloxacin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 14763781-0 2003 Fluoride release from NaF- and AmF-impregnated toothpicks and dental flosses in vitro and in vivo. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 14550561-3 2003 We now show that synthetic poly-L-histidine (Hn) binds to LPS and abrogates the release of the proinflammatory cytokine interleukin-8 (IL-8) in LPS-stimulated human whole blood. polyhistidine 27-43 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 14550561-3 2003 We now show that synthetic poly-L-histidine (Hn) binds to LPS and abrogates the release of the proinflammatory cytokine interleukin-8 (IL-8) in LPS-stimulated human whole blood. polyhistidine 27-43 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 14550561-3 2003 We now show that synthetic poly-L-histidine (Hn) binds to LPS and abrogates the release of the proinflammatory cytokine interleukin-8 (IL-8) in LPS-stimulated human whole blood. polyhistidine 45-47 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 14550561-3 2003 We now show that synthetic poly-L-histidine (Hn) binds to LPS and abrogates the release of the proinflammatory cytokine interleukin-8 (IL-8) in LPS-stimulated human whole blood. polyhistidine 45-47 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 14763781-9 2003 An interdental brush dipped in 0.2% NaF gel and a mouthrinse with 0.2% NaF resulted in elevated fluoride concentrations at the same level as when multiple toothpicks were used. Fluorides 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 14763781-9 2003 An interdental brush dipped in 0.2% NaF gel and a mouthrinse with 0.2% NaF resulted in elevated fluoride concentrations at the same level as when multiple toothpicks were used. Fluorides 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 14672330-5 2003 RESULTS: Simple regression analysis demonstrated a significant negative correlation between the concentrations of IL-8 and oxygen in FF (r = 0.50, P < 0.0001). Oxygen 123-129 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 12907466-8 2003 Sugar phloem unloading was significantly inhibited by the inclusion of either 7.5 mm NaF or 2.5 mm PCMB in the buffer solution. Sugars 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 14612204-0 2003 Hypoxia increases 25-hydroxycholesterol-induced interleukin-8 protein secretion in human macrophages. 25-hydroxycholesterol 18-39 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 14530017-9 2003 ONO-6818 significantly reduced interleukin 8 and C5b-9 production. ONO 6818 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 14530017-12 2003 CONCLUSIONS: Inhibition of neutrophil elastase activity with ONO-6818 reduces further interleukin 8 production and the formation of the complement membrane attack complex, and this results in a reduction of neutrophil elastase levels during simulated extracorporeal circulation. ONO 6818 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 14612204-3 2003 The aim of this study was to investigate the effect of hypoxia on the secretion of IL-8 by oxysterol-stimulated macrophages. Oxysterols 91-100 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 14612204-4 2003 Hypoxia enhances 25-hydroxycholesterol (25-OH-chol)-induced IL-8 secretion in human monocyte-derived macrophages. 25-hydroxycholesterol 17-38 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 14612204-4 2003 Hypoxia enhances 25-hydroxycholesterol (25-OH-chol)-induced IL-8 secretion in human monocyte-derived macrophages. 25-oh-chol 40-50 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 14505796-4 2003 Human CXCL8 produced in vivo neutrophilia, chemotaxis and intracellular calcium release of guinea pig neutrophils. Calcium 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 6-11 14612204-8 2003 These observations suggest that similar intracellular signalling pathways are used for both 25-OH-chol-induced IL-8 expression and hypoxia-induced IL-8 expression. 25-oh-chol 92-102 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 14612204-9 2003 Thus, hypoxia in atherosclerotic plaques may increase the secretion of IL-8 from oxysterol-containing foam cells, which subsequently may accelerate the progression of atherosclerosis. Oxysterols 81-90 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 12919783-4 2003 The findings suggest that GEP and high-sulfur DEP induced the production of similar levels of IL-8 by unprimed A549 cells. Sulfur 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 14522840-3 2003 Novel data show that oATP reduces NFkappaB activation and IL-8 release in cells lacking P2X7R, thus suggesting that some anti-inflammatory effects of oATP may not be due to blockade of the P2X7R. 2',3'-dialdehyde ATP 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 14522842-5 2003 Attenuation of TNF-alpha-stimulated IL-8 secretion by oATP was similar in wild-type HEK cells or HEK cells stably expressing recombinant P2X7R. 2',3'-dialdehyde ATP 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 12919783-5 2003 The level of IL-8 produced by unprimed A549 cells in response to low-sulfur DEP was found lower than that produced in response to high-sulfur DEP and GEP. Sulfur 69-75 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 12919783-5 2003 The level of IL-8 produced by unprimed A549 cells in response to low-sulfur DEP was found lower than that produced in response to high-sulfur DEP and GEP. Sulfur 135-141 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 14519149-5 2003 RESULTS: Following RV16-infection, a significant increase in IL-8 was observed in the placebo- and budesonide-treated asthmatics (P=0.033 and 0.037, respectively), whereas IL-1beta only increased in the two asthma groups combined (P=0.035). Budesonide 99-109 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 14553834-0 2003 8-isoprostane increases expression of interleukin-8 in human macrophages through activation of mitogen-activated protein kinases. 8-epi-prostaglandin F2alpha 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 14553834-3 2003 We therefore investigated the effects of 8-isoprostane on the expression of inflammatory chemokines with consciousness on IL-8 (mRNA and protein) in human macrophages. 8-epi-prostaglandin F2alpha 41-54 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 14553834-5 2003 METHODS AND RESULTS: 8-isoprostane (10 microM) induced IL-8 expression (mRNA and protein), measured by real-time quantitative RT-PCR and enzyme immunoassay, respectively, in both THP-1 macrophages and human monocyte-derived macrophages. 8-epi-prostaglandin F2alpha 21-34 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 14553834-8 2003 Furthermore, the ERK 1/2 inhibitor, PD98059, and the p38 MAPK inhibitor, SB203580, markedly reduced 8-isoprostane-induced IL-8 expression (mRNA and protein), while inhibition of NF-kappaB activation and translocation had no significant effect on IL-8 expression. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 36-43 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 14553834-8 2003 Furthermore, the ERK 1/2 inhibitor, PD98059, and the p38 MAPK inhibitor, SB203580, markedly reduced 8-isoprostane-induced IL-8 expression (mRNA and protein), while inhibition of NF-kappaB activation and translocation had no significant effect on IL-8 expression. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 36-43 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 14553834-8 2003 Furthermore, the ERK 1/2 inhibitor, PD98059, and the p38 MAPK inhibitor, SB203580, markedly reduced 8-isoprostane-induced IL-8 expression (mRNA and protein), while inhibition of NF-kappaB activation and translocation had no significant effect on IL-8 expression. SB 203580 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 14553834-8 2003 Furthermore, the ERK 1/2 inhibitor, PD98059, and the p38 MAPK inhibitor, SB203580, markedly reduced 8-isoprostane-induced IL-8 expression (mRNA and protein), while inhibition of NF-kappaB activation and translocation had no significant effect on IL-8 expression. SB 203580 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 14553834-8 2003 Furthermore, the ERK 1/2 inhibitor, PD98059, and the p38 MAPK inhibitor, SB203580, markedly reduced 8-isoprostane-induced IL-8 expression (mRNA and protein), while inhibition of NF-kappaB activation and translocation had no significant effect on IL-8 expression. 8-epi-prostaglandin F2alpha 100-113 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 14553834-8 2003 Furthermore, the ERK 1/2 inhibitor, PD98059, and the p38 MAPK inhibitor, SB203580, markedly reduced 8-isoprostane-induced IL-8 expression (mRNA and protein), while inhibition of NF-kappaB activation and translocation had no significant effect on IL-8 expression. 8-epi-prostaglandin F2alpha 100-113 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 14553834-9 2003 CONCLUSIONS: We show that 8-isoprostane increases IL-8 expression in human macrophages involving both ERK 1/2 and p38 MAPK, but not NF-kappaB signaling pathway. 8-epi-prostaglandin F2alpha 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 14500470-7 2003 The results indicated that the p38 mitogen-activated protein kinase (MAPK) and Src-dependent Raf-1-Mek1/2-extracellular signal-regulated kinase mitogen-activated protein kinase (ERK MAPK) pathways are required for NTHI-induced IL-8 production. nthi 214-218 C-X-C motif chemokine ligand 8 Homo sapiens 227-231 14627349-14 2003 (4) COX-2, PPARgamma, Bcl-2, and survivin were overexpressed in gastric tumor, but the inhibition of COX-2 activity by Vioxx resulted in a significant reduction in serum and tumor levels of progastrin and gastrin and serum IL-8 and TNF-alpha levels, suggesting that gastrin and proinflammatory cytokines could mediate the up-regulation of COX-2 in gastric cancerogenesis. rofecoxib 119-124 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 12946434-0 2003 The diesel exhaust component pyrene induces expression of IL-8 but not of eotaxin. pyrene 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12946434-3 2003 We have characterized the influence of pyrene, a polycyclic aromatic hydrocarbon (PAH) contained, for example, in diesel exhaust particles (DEP), on transcription and secretion of the chemokines interleukin-8 (IL-8) and eotaxin. pyrene 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 195-208 12946434-3 2003 We have characterized the influence of pyrene, a polycyclic aromatic hydrocarbon (PAH) contained, for example, in diesel exhaust particles (DEP), on transcription and secretion of the chemokines interleukin-8 (IL-8) and eotaxin. pyrene 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 12946434-3 2003 We have characterized the influence of pyrene, a polycyclic aromatic hydrocarbon (PAH) contained, for example, in diesel exhaust particles (DEP), on transcription and secretion of the chemokines interleukin-8 (IL-8) and eotaxin. Polycyclic Aromatic Hydrocarbons 49-80 C-X-C motif chemokine ligand 8 Homo sapiens 195-208 12946434-3 2003 We have characterized the influence of pyrene, a polycyclic aromatic hydrocarbon (PAH) contained, for example, in diesel exhaust particles (DEP), on transcription and secretion of the chemokines interleukin-8 (IL-8) and eotaxin. Polycyclic Aromatic Hydrocarbons 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 195-208 12946434-6 2003 Promoter activity, mRNA production and protein expression of IL-8 were increased by pyrene. pyrene 84-90 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 12950106-4 2003 Furthermore, GTPgammaS and NaF stimulated cAMP, but GDPbetaS and mastoparan had no apparent effect, consistent with recent evidence that G(s), but not G(i), contributes to AC/cAMP regulation in uncapacitated cells. Cyclic AMP 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 14514769-5 2003 Among the toxic dioxins proposed by the World Health Organization (WHO) in 1998, 2,3",4,4",5-pentachlorobiphenyl (PCB 118) and OCDD, which were mainly found in saliva, significantly induced IL-8 production in HGEC. Dioxins 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 14514769-5 2003 Among the toxic dioxins proposed by the World Health Organization (WHO) in 1998, 2,3",4,4",5-pentachlorobiphenyl (PCB 118) and OCDD, which were mainly found in saliva, significantly induced IL-8 production in HGEC. 2,3',4,4',5-pentachlorobiphenyl 81-112 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 14514769-5 2003 Among the toxic dioxins proposed by the World Health Organization (WHO) in 1998, 2,3",4,4",5-pentachlorobiphenyl (PCB 118) and OCDD, which were mainly found in saliva, significantly induced IL-8 production in HGEC. Polychlorinated Biphenyls 114-117 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 14514769-5 2003 Among the toxic dioxins proposed by the World Health Organization (WHO) in 1998, 2,3",4,4",5-pentachlorobiphenyl (PCB 118) and OCDD, which were mainly found in saliva, significantly induced IL-8 production in HGEC. octachlorodibenzo-4-dioxin 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 14514769-6 2003 Furthermore, these two dioxins markedly augmented IL-8 production stimulated with fimbriae from Porphyromonas gingivalis, which is well-known as a pathogenic factor in periodontal diseases. Dioxins 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12777636-10 2003 Furthermore, inhibition was dependent on the stimulus; IL-6, IL-8, IL-1 beta and TNF alpha production induced by LOS or SAC was only slightly decreased by methotrexate. Methotrexate 155-167 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 13679572-6 2003 IL-8 secretion was inhibited by pertussis toxin and a selective p38 kinase inhibitor, SB203580. SB 203580 86-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12925902-8 2003 The norepinephrine dosage used in the ICU correlated with plasma IL-8 levels 2 hours after arriving in the ICU (r = 0.56, p = 0.031). Norepinephrine 4-18 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 13679572-7 2003 The CysLT2 response may permit the cys-LTs and nucleotides generated in infection and tissue injury to elicit IL-8 generation by hMCs, potentially leading to neutrophilic infiltration, a characteristic of aerosol challenge-induced late-phase responses and of sudden death associated with asthma. cysteinyl-leukotriene 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 12763941-3 2003 The inhibition of PI3K activity with wortmannin showed that rate of pseudopod extension stimulated with N-formyl-Met-Leu-Phe (fMLP was mostly dependent on PI3K, while the rate of interleukin-8 (IL-8)-stimulated pseudopod extension was less dependent on PI3K. Wortmannin 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 179-192 12951051-0 2003 Reduction of chemokine IL-8 and RANTES expression in human bronchial epithelial cells by a sea-water derived saline through inhibited nuclear factor-kappaB activation. Water 95-100 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 12951051-0 2003 Reduction of chemokine IL-8 and RANTES expression in human bronchial epithelial cells by a sea-water derived saline through inhibited nuclear factor-kappaB activation. Sodium Chloride 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 12951051-3 2003 Exposure of BECs to ISW saline caused a significant decrease in IL-8 and RANTES gene expression and protein production as compared to that observed with 0.9% NaCl saline. Sodium Chloride 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 12763941-3 2003 The inhibition of PI3K activity with wortmannin showed that rate of pseudopod extension stimulated with N-formyl-Met-Leu-Phe (fMLP was mostly dependent on PI3K, while the rate of interleukin-8 (IL-8)-stimulated pseudopod extension was less dependent on PI3K. N-Formylmethionine Leucyl-Phenylalanine 104-124 C-X-C motif chemokine ligand 8 Homo sapiens 179-192 12763941-3 2003 The inhibition of PI3K activity with wortmannin showed that rate of pseudopod extension stimulated with N-formyl-Met-Leu-Phe (fMLP was mostly dependent on PI3K, while the rate of interleukin-8 (IL-8)-stimulated pseudopod extension was less dependent on PI3K. N-Formylmethionine Leucyl-Phenylalanine 104-124 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 12816876-5 2003 Three- to 4-fold increases in MCP-1 and IL-8 release were observed at endotoxin concentrations of 100 pg/mL; these increases were inhibited by the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor atorvastatin. Atorvastatin 205-217 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 14666669-1 2003 We have recently found that millimolar concentrations of sodium fluoride (NaF) induced apoptotic cell death, characterized by caspase activation and DNA fragmentation, in tumor cell lines. Sodium Fluoride 57-72 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 12824191-6 2003 Both specific inhibitors of p38 MAP kinase and sodium vanadate, a potent protein-tyrosine phosphatase inhibitor, blocked IL-8 production in a dose-dependent manner. Vanadates 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 12921778-4 2003 We show that okadaic acid (OA), an inhibitor of protein phosphatases PP1 and PP2A, induces sustained activation of NFkappaB and degradation of the nuclear IkappaBalpha, and increases interleukin-8 expression in the neutrophils. Okadaic Acid 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 183-196 12921778-4 2003 We show that okadaic acid (OA), an inhibitor of protein phosphatases PP1 and PP2A, induces sustained activation of NFkappaB and degradation of the nuclear IkappaBalpha, and increases interleukin-8 expression in the neutrophils. Okadaic Acid 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 183-196 14666669-8 2003 During the cell death induction in human promyelocytic leukemia HL-60 cells by NaF, the consumption of glucose rapidly declined, followed by a decline in the consumption of major amino acids. Glucose 103-110 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 14666669-9 2003 The present study suggests that the cytotoxic activity of NaF is not regulated by the redox mechanism, but rather linked to the rapid decline in glucose consumption at early stage. Glucose 145-152 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 12940901-2 2003 Many water-soluble mediators with pro- and anti-inflammatory action such as TNF, IL-6, IL-8, and IL-10 play a strategic role in septic syndrome. Water 5-10 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 12941142-6 2003 Furthermore, IL-8 production in PBMC stimulated with the active monosaccharide lipid A analogues as well as compound 506 was clearly inhibited by the monoclonal antibody to human TLR4. PBMC 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 14621001-4 2003 The corrosion resistance of titanium decreased as the NaF concentration increased and as pH decreased. Titanium 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 12970036-10 2003 RESULTS: and measurements: EBC NO(2)(-) correlated well with VT (milliliters per kilogram of BW; r = 0.79, p < 0.0001) and expiratory minute volume (r = 0.60, p < 0.0001) but not with other ventilatory parameters or parameters of pulmonary (EBC IL-6, EBC IL-8) or systemic (serum IL-6, IL-8, and procalcitonin) inflammation. NSC638702 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 261-265 12970036-10 2003 RESULTS: and measurements: EBC NO(2)(-) correlated well with VT (milliliters per kilogram of BW; r = 0.79, p < 0.0001) and expiratory minute volume (r = 0.60, p < 0.0001) but not with other ventilatory parameters or parameters of pulmonary (EBC IL-6, EBC IL-8) or systemic (serum IL-6, IL-8, and procalcitonin) inflammation. NSC638702 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 292-296 12941142-6 2003 Furthermore, IL-8 production in PBMC stimulated with the active monosaccharide lipid A analogues as well as compound 506 was clearly inhibited by the monoclonal antibody to human TLR4. Monosaccharides 64-78 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 12941142-6 2003 Furthermore, IL-8 production in PBMC stimulated with the active monosaccharide lipid A analogues as well as compound 506 was clearly inhibited by the monoclonal antibody to human TLR4. Lipid A 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 14566081-0 2003 Poly-C specific ribonuclease activity correlates with increased concentrations of IL-6, IL-8 and sTNFR55/sTNFR75 in plasma of patients with acute pancreatitis. Poly C 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12928590-6 2003 Diphenylene iodonium, an inhibitor of NADPH oxidase, significantly inhibited CMV-induced IL-8 production and promotion of serum-induced DNA synthesis. diphenyleneiodonium 0-20 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 14502144-9 2003 Interleukin-6 and interleukin-8 concentrations correlated with the length of inotropic support, as well as with the length of mechanical ventilation (r >.70, P </=.0006), and were inversely related to the ratio of arterial oxygen tension to fraction of inspired oxygen. Oxygen 229-235 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 14502144-9 2003 Interleukin-6 and interleukin-8 concentrations correlated with the length of inotropic support, as well as with the length of mechanical ventilation (r >.70, P </=.0006), and were inversely related to the ratio of arterial oxygen tension to fraction of inspired oxygen. Oxygen 268-274 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 12946798-7 2003 RESULTS: Leukocytes incubated with Dextran-70 demonstrated greater than a 6-fold (p < 0.05) increase in the expression of interleukin-8, growth-regulated oncogenes alpha and beta, L-selectin, superoxide dismutase, tumor necrosis factor-alpha (TNF-alpha), and mitogen-activated protein kinase 3. Dextrans 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 125-138 14558594-2 2003 The results show that thalidomide inhibits endotelial cell proliferation induced by bFGF and VEGF, more so if the cells are grown on vitronectin; moreover, treatment with thalidomide reduces the release of MMP-2 and IL-8 by endothelial cells, suggesting a further pathway for the antiangiogenic activity of drug. Thalidomide 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 14558594-2 2003 The results show that thalidomide inhibits endotelial cell proliferation induced by bFGF and VEGF, more so if the cells are grown on vitronectin; moreover, treatment with thalidomide reduces the release of MMP-2 and IL-8 by endothelial cells, suggesting a further pathway for the antiangiogenic activity of drug. Thalidomide 171-182 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 12947130-10 2003 QPT was negatively correlated with CXCL8 and positively correlated with IGF-I and lung transfer factor in hospitalised and in stable patients. qpt 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 12626343-1 2003 Peroxynitrite, formed by nitric oxide and superoxide, has been shown to nitrate and reduce the function of proinflammatory proteins such as interleukin (IL)-8, monocyte chemoattractant protein-1, and eotaxin, but in contrast, to enhance the function of the anti-inflammatory cytokine IL-10 in reducing IL-1 release from blood monocytes. Peroxynitrous Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 140-158 12881478-8 2003 These data indicate that pathophysiological levels of Hcy can alter human monocyte function by upregulating MCP-1 and IL-8 expression and secretion via enhanced formation of intracellular ROS originated from NAD(P)H oxidase source via calmodulin or protein kinase C signaling pathways and that Hcy-induced ROS subsequently activates mitogen-activated protein kinase (p38 and ERK1/2) and nuclear factor-kappaB in a PPARgamma activator-sensitive manner. Homocysteine 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 12915334-12 2003 In these experiments EPA was the omega-3 fatty acid responsible for improvement, with distinct effects on inhibition of cytokines formation (IL-1 to IL-6, IL-8, TFN-alpha, GM-CSF), decreased induction of proinflammatory adhesion molecules (selectines, intercellular adhesions molecule-1 (ICAM-1)), and degrading enzymes (e.g. phospholipase A2, cyclooxygenase-2, inducible NO-synthetase). Fatty Acids, Omega-3 33-51 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 12901923-0 2003 Synthesis and structure-activity relationship of 2-amino-3-heteroaryl-quinoxalines as non-peptide, small-molecule antagonists for interleukin-8 receptor. 2-amino-3-heteroaryl-quinoxalines 49-82 C-X-C motif chemokine ligand 8 Homo sapiens 130-143 12902511-4 2003 In endothelial culture supernatants, IL-8 was detected in a trimolecular complex with heparan sulfate and syndecan-1. Heparitin Sulfate 86-101 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 12902511-6 2003 Increased shedding of IL-8/heparan sulfate/syndecan-1 complexes was accompanied by inhibition of neutrophil transendothelial migration, and aprotinin, a potent plasmin inhibitor, reversed this inhibition. heparan 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 12881478-0 2003 Homocysteine mediated expression and secretion of monocyte chemoattractant protein-1 and interleukin-8 in human monocytes. Homocysteine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 12881478-5 2003 We found that clinically relevant levels of Hcy (10 to 1000 micromol/L) increased the protein secretion and mRNA expression as well as activity of MCP-1 and IL-8 in cultured primary human monocytes. Homocysteine 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 12626343-1 2003 Peroxynitrite, formed by nitric oxide and superoxide, has been shown to nitrate and reduce the function of proinflammatory proteins such as interleukin (IL)-8, monocyte chemoattractant protein-1, and eotaxin, but in contrast, to enhance the function of the anti-inflammatory cytokine IL-10 in reducing IL-1 release from blood monocytes. Nitric Oxide 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 140-158 12626343-1 2003 Peroxynitrite, formed by nitric oxide and superoxide, has been shown to nitrate and reduce the function of proinflammatory proteins such as interleukin (IL)-8, monocyte chemoattractant protein-1, and eotaxin, but in contrast, to enhance the function of the anti-inflammatory cytokine IL-10 in reducing IL-1 release from blood monocytes. Superoxides 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 140-158 12873450-8 2003 Baicalin did not suppress IL-1beta-induced IL-6 and IL-8 production, but dexamethasone, baicalein, and wogonin, significantly suppressed IL-6 and IL-8 production. Dexamethasone 73-86 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 12880609-8 2003 IL-8 and IL-6 production from stimulated biopsies significantly decreased with increasing glutamine concentration from 0.5 to 10mM, (2543 [828-3634] to 1499 [282-2617] for IL-8, 62 [22-117] to 24 [12-99] for IL-6, both P<0.05), whereas IL-10 production was increased (0.7 [0.2-1.6] to 1.2 [2.6-0.5],P<0.05). Glutamine 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12880609-8 2003 IL-8 and IL-6 production from stimulated biopsies significantly decreased with increasing glutamine concentration from 0.5 to 10mM, (2543 [828-3634] to 1499 [282-2617] for IL-8, 62 [22-117] to 24 [12-99] for IL-6, both P<0.05), whereas IL-10 production was increased (0.7 [0.2-1.6] to 1.2 [2.6-0.5],P<0.05). Glutamine 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 12880609-11 2003 CONCLUSIONS: Glutamine was shown in human intestinal mucosa to reduce the production of the pro-inflammatory cytokines IL-6 and IL-8, and enhance the production of the anti-inflammatory cytokine, IL-10. Glutamine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 12881351-10 2003 Correlation coefficients showed that the spermidine and putrescine level variations correlated with the VEGF and IL-8 content in the active PDR and PVR groups, but not in those with quiescent PDR patients, while spermine was correlated to these cytokines in PDR, but not in PVR groups. Spermidine 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 12881351-10 2003 Correlation coefficients showed that the spermidine and putrescine level variations correlated with the VEGF and IL-8 content in the active PDR and PVR groups, but not in those with quiescent PDR patients, while spermine was correlated to these cytokines in PDR, but not in PVR groups. Putrescine 56-66 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 12964812-0 2003 Stimulatory effect of homocysteine on interleukin-8 expression in human endothelial cells. Homocysteine 22-34 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 12964812-4 2003 The objective of the present study was to investigate the effect of homocysteine on interleukin-8 production in human endothelial cells. Homocysteine 68-80 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 12964812-5 2003 Cells were incubated with various concentrations of homocysteine for 20 h. The gene expression was determined by real-time PCR and the interleukin-8 protein was measured by immunoassay analysis. Homocysteine 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 135-148 12964812-6 2003 Homocysteine enhanced the expression of interleukin-8 in a dose-dependent manner (181% of controls at 2.5 mmol/l homocysteine). Homocysteine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 12964812-6 2003 Homocysteine enhanced the expression of interleukin-8 in a dose-dependent manner (181% of controls at 2.5 mmol/l homocysteine). Homocysteine 113-125 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 12964812-7 2003 Stimulation of gene expression was associated with a parallel increase in interleukin-8 protein synthesis (160% of controls at 5.0 mmol/l homocysteine). Homocysteine 138-150 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 12964812-8 2003 By co-incubation of endothelial cells with homocysteine and copper sulfate, a further elevation of interleukin-8 expression (251% of controls) was observed, whereas copper sulfate alone had no stimulatory effect. Homocysteine 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 99-112 12964812-8 2003 By co-incubation of endothelial cells with homocysteine and copper sulfate, a further elevation of interleukin-8 expression (251% of controls) was observed, whereas copper sulfate alone had no stimulatory effect. Copper Sulfate 60-74 C-X-C motif chemokine ligand 8 Homo sapiens 99-112 12964812-9 2003 In conclusion, the present study demonstrated that homocysteine altered endothelial cell function by stimulating interleukin-8 expression, suggesting a contribution of homocysteine to the initiation and progression of atherosclerosis. Homocysteine 51-63 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 12964812-9 2003 In conclusion, the present study demonstrated that homocysteine altered endothelial cell function by stimulating interleukin-8 expression, suggesting a contribution of homocysteine to the initiation and progression of atherosclerosis. Homocysteine 168-180 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 12873450-8 2003 Baicalin did not suppress IL-1beta-induced IL-6 and IL-8 production, but dexamethasone, baicalein, and wogonin, significantly suppressed IL-6 and IL-8 production. baicalein 88-97 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 12873450-8 2003 Baicalin did not suppress IL-1beta-induced IL-6 and IL-8 production, but dexamethasone, baicalein, and wogonin, significantly suppressed IL-6 and IL-8 production. wogonin 103-110 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 12873450-9 2003 Elevation of IL-6 and IL-8 mRNA was not suppressed by baicalin but was significantly suppressed by dexamethasone, baicalein, and wogonin. Dexamethasone 99-112 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 12748173-0 2003 Transcriptional regulation of interleukin (IL)-8 by bradykinin in human airway smooth muscle cells involves prostanoid-dependent activation of AP-1 and nuclear factor (NF)-IL-6 and prostanoid-independent activation of NF-kappaB. Prostaglandins 108-118 C-X-C motif chemokine ligand 8 Homo sapiens 30-48 12748173-0 2003 Transcriptional regulation of interleukin (IL)-8 by bradykinin in human airway smooth muscle cells involves prostanoid-dependent activation of AP-1 and nuclear factor (NF)-IL-6 and prostanoid-independent activation of NF-kappaB. Prostaglandins 181-191 C-X-C motif chemokine ligand 8 Homo sapiens 30-48 12748173-7 2003 Furthermore, exogenous prostaglandin E2 stimulated AP-1 and NF-IL-6 binding to the IL-8 promoter. Dinoprostone 23-39 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 12748173-6 2003 Indomethacin, a cyclooxygenase inhibitor, partially inhibited IL-8 release and the promoter binding of AP-1 and NF-IL-6, but not NF-kappaB. Indomethacin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 12748173-10 2003 Transcriptional activation of the IL-8 promoter by BK involves the prostanoid-independent activation of NF-kappaB, and prostanoid-dependent activation of AP-1 and NF-IL-6 plays a key role in augmenting the response. Prostaglandins 67-77 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 12953027-10 2003 The ratio between the total sodium concentration in the ultrafiltrate (NaF(uf)) and NaF(pw) (alpha) at the post-reinfusion site was 0.96 and decreased to 0.94 when NaF(pw) values at the pre-reinfusion site were considered. Sodium 28-34 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 12897563-4 2003 Further, the effects of clarithromycin, a 14-member ring macrolide, on IL-8 gene expression and nuclear factor-kappa B (NF-kappa B) activation in adenoidal fibroblasts were evaluated. Clarithromycin 24-38 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 12897563-11 2003 Treatment of cells with the NF-kappa B inhibitor N-tosyl-(L)-phenylalanine chloromethyl ketone, as well as with clarithromycin, reduced expression of IL-8 and NF-kappa B activity in a dose-dependent manner. Tosylphenylalanyl Chloromethyl Ketone 49-94 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 12897563-11 2003 Treatment of cells with the NF-kappa B inhibitor N-tosyl-(L)-phenylalanine chloromethyl ketone, as well as with clarithromycin, reduced expression of IL-8 and NF-kappa B activity in a dose-dependent manner. Clarithromycin 112-126 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 12897563-13 2003 The inhibitory effects of clarithromycin on NF-kappa B activation and IL-8 production in adenoidal fibroblasts might explain, in part, the mechanism of this drug in improving otitis media with effusion. Clarithromycin 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 12939465-0 2003 Dacarbazine causes transcriptional up-regulation of interleukin 8 and vascular endothelial growth factor in melanoma cells: a possible escape mechanism from chemotherapy. Dacarbazine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 12939465-10 2003 Metastatic melanoma cell lines secreting high levels of IL-8 and VEGF were more resistant to DTIC than early primary melanomas secreting low levels of the cytokines. Dacarbazine 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 12939465-11 2003 In addition, transfection of the primary cutaneous melanoma SB-2 cells with the IL-8 gene rendered them resistant to the cytotoxic effect of the drug, whereas the addition of IL-8-neutralizing antibody to metastatic melanoma cells lowered their sensitivity to DTIC. Dacarbazine 260-264 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 12939465-12 2003 Taken together, our data demonstrate that DTIC can cause melanoma cells to secrete IL-8 and VEGF, which might render them resistant to the cytotoxic effects of the drug. Dacarbazine 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 12939465-13 2003 We propose that combination treatment with anti-VEGF/IL-8 agents may potentiate the therapeutic effects of DTIC. Dacarbazine 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 12953027-10 2003 The ratio between the total sodium concentration in the ultrafiltrate (NaF(uf)) and NaF(pw) (alpha) at the post-reinfusion site was 0.96 and decreased to 0.94 when NaF(pw) values at the pre-reinfusion site were considered. Sodium 28-34 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 12894071-6 2003 IL-8 production stimulated with histamine was also suppressed by cetirizine, ketotifen, and olopatadine. Histamine 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12953027-10 2003 The ratio between the total sodium concentration in the ultrafiltrate (NaF(uf)) and NaF(pw) (alpha) at the post-reinfusion site was 0.96 and decreased to 0.94 when NaF(pw) values at the pre-reinfusion site were considered. Sodium 28-34 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 12894071-6 2003 IL-8 production stimulated with histamine was also suppressed by cetirizine, ketotifen, and olopatadine. Cetirizine 65-75 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12883201-11 2003 The cold/rewarming-induced IL-8 production was reduced to approximately 50% by introducing an antisense oligonucleotide for the p65 subunit of NF-kappaB and by treatment with N-acetyl-leucinyl-leucinyl-norleucinal and pyrrolidine dithiocarbamate. Oligonucleotides 104-119 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 12894071-6 2003 IL-8 production stimulated with histamine was also suppressed by cetirizine, ketotifen, and olopatadine. Ketotifen 77-86 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12894071-6 2003 IL-8 production stimulated with histamine was also suppressed by cetirizine, ketotifen, and olopatadine. Olopatadine Hydrochloride 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12913774-8 2003 CONCLUSION: Dexamethasone does not cause an impaired decline of tracheal RSV but lowers IL-8 of children mechanically ventilated for RSV lower respiratory tract infection, potentially leading to less inflammation and reduced phagocyte activation. Dexamethasone 12-25 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12947311-9 2003 IL-8 production in response to lipopolysaccharide and xanthine oxidase was inhibited significantly by hemin exposure, although PGI(2) production was not affected. Hemin 102-107 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12865660-0 2003 Copper stimulates the synthesis and release of interleukin-8 in human endothelial cells: a possible early role in systemic inflammatory responses. Copper 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 12865660-1 2003 Endogenous copper can play an important role in postischemic reperfusion injury, a condition associated with endothelial cell activation and increased interleukin 8 (IL-8) production. Copper 11-17 C-X-C motif chemokine ligand 8 Homo sapiens 151-164 12865660-1 2003 Endogenous copper can play an important role in postischemic reperfusion injury, a condition associated with endothelial cell activation and increased interleukin 8 (IL-8) production. Copper 11-17 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 12865660-3 2003 No previous reports have indicated that copper has a direct role in stimulating human endothelial IL-8 secretion. Copper 40-46 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 12865660-4 2003 Increased IL-8 in the culture medium of human umbilical vein (HUVEC), lung microvascular, and iliac artery endothelial cells was observed 24 h after the addition of 10 to 50 microM CuCl2 (cupric ions). cupric chloride 181-186 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 12865660-5 2003 HUVEC IL-8 induction by copper was higher than by 50 pg/mL tumor necrosis factor-alpha, whereas 50 pg/mL IL-1beta and 1 ng/mL platelet-activating factor did not stimulate IL-8 production or release. Copper 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 12865660-6 2003 HUVEC IL-8 mRNA increased 3 h after CuCl2 stimulation and remained elevated after 24 h, implying sustained transcriptional activation. cupric chloride 36-41 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 12865660-8 2003 Cu(II) appeared to be the primary copper ion responsible for the observed increase in IL-8 because a specific high-affinity Cu(II)-binding peptide, d-Asp-d-Ala-d-His-d-Lys (d-DAHK), completely abolished this effect in a dose-dependent manner. cu(ii) 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12865660-8 2003 Cu(II) appeared to be the primary copper ion responsible for the observed increase in IL-8 because a specific high-affinity Cu(II)-binding peptide, d-Asp-d-Ala-d-His-d-Lys (d-DAHK), completely abolished this effect in a dose-dependent manner. Copper 34-40 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12865660-8 2003 Cu(II) appeared to be the primary copper ion responsible for the observed increase in IL-8 because a specific high-affinity Cu(II)-binding peptide, d-Asp-d-Ala-d-His-d-Lys (d-DAHK), completely abolished this effect in a dose-dependent manner. cu(ii) 124-130 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12865660-8 2003 Cu(II) appeared to be the primary copper ion responsible for the observed increase in IL-8 because a specific high-affinity Cu(II)-binding peptide, d-Asp-d-Ala-d-His-d-Lys (d-DAHK), completely abolished this effect in a dose-dependent manner. d-asp-d-ala-d-his 148-165 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12865660-8 2003 Cu(II) appeared to be the primary copper ion responsible for the observed increase in IL-8 because a specific high-affinity Cu(II)-binding peptide, d-Asp-d-Ala-d-His-d-Lys (d-DAHK), completely abolished this effect in a dose-dependent manner. D-Lysine 166-171 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12865660-8 2003 Cu(II) appeared to be the primary copper ion responsible for the observed increase in IL-8 because a specific high-affinity Cu(II)-binding peptide, d-Asp-d-Ala-d-His-d-Lys (d-DAHK), completely abolished this effect in a dose-dependent manner. dahk 175-179 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12865660-9 2003 These results suggest that Cu(II) may induce endothelial IL-8 by a mechanism independent of known Cu(I) generation of reactive oxygen species. cu(ii) 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 12865660-10 2003 Furthermore, in vivo studies are warranted to determine if copper is involved in the pathogenesis of systemic inflammation and if Cu(II) chelation can reduce this IL-8-induced endothelial inflammatory response. cu(ii) 130-136 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 14642174-4 2003 RESULTS: There was a significant increase in plasma levels of IL-8 and both adhesion molecules [IL-8 (247.4 +/- 84.2) microg/L (P < 0.01); sICAM-1 (530.3 +/- 286.1) microg/L (P = 0.002 7); sVCAM-1 (575.3 +/- 350.4) microg/L (P = 0.001 3)] during the mobilization process; furthermore, IL-8 and sVCAM-1 concentration in the patient"s plasma was paralleled to the numbers of CD(34)(+) cell, CFU-GM, WBC and BPC (P < 0.001). Cadmium 376-378 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 14642174-4 2003 RESULTS: There was a significant increase in plasma levels of IL-8 and both adhesion molecules [IL-8 (247.4 +/- 84.2) microg/L (P < 0.01); sICAM-1 (530.3 +/- 286.1) microg/L (P = 0.002 7); sVCAM-1 (575.3 +/- 350.4) microg/L (P = 0.001 3)] during the mobilization process; furthermore, IL-8 and sVCAM-1 concentration in the patient"s plasma was paralleled to the numbers of CD(34)(+) cell, CFU-GM, WBC and BPC (P < 0.001). S-(4-bromophenyl)cysteine sulfoxide 408-411 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 12883201-11 2003 The cold/rewarming-induced IL-8 production was reduced to approximately 50% by introducing an antisense oligonucleotide for the p65 subunit of NF-kappaB and by treatment with N-acetyl-leucinyl-leucinyl-norleucinal and pyrrolidine dithiocarbamate. pyrrolidine dithiocarbamic acid 218-245 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 14506934-2 2003 This study investigated the possible effects of IL-1alpha, tumor necrosis factor-alpha (TNF-alpha), protein kinase C (PKC) activators (TPA), and db-cyclic adenosine monophosphate (cAMP) on IL-8 and GRO-alpha production by immortalized GC1a and granulosa-lutein cells. db-cyclic adenosine monophosphate 145-178 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 12821113-6 2003 In addition, DFX significantly increased the production of IL-6, IL-8, and TNF-alpha in HMC-1 (P<0.05). Deferoxamine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 12925148-3 2003 Effects of PGs on the production of other cytokines such as interleukin (IL)-6 and IL-8 have been controversial. Prostaglandins 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 12925148-9 2003 Reb suppressed PGE1 -, but not 15d-PGJ2-, induced increase of IL-6 and IL-8 production. Alprostadil 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 12818968-0 2003 Dobutamine modulates lipopolysaccharide-induced macrophage inflammatory protein-1alpha and interleukin-8 production in human monocytes. Dobutamine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 12818968-3 2003 We conducted this study to investigate the effect of dobutamine on lipopolysaccharide (LPS)-induced MIP-1alpha and IL-8 production by human monocytic THP-1 cells. Dobutamine 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 12840601-8 2003 RESULTS: Urinary IL-8 during relapse was significantly increased when compared with that of during remission or controls (13,996 +/- 2,811 vs. 2,941 +/- 373, 5,331 +/- 640 ng/mg.cr) (p < 0.05). Chromium 57-59 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 12818968-6 2003 Dobutamine significantly inhibited LPS-induced MIP-1alpha and IL-8 production by THP-1 cells in a dose-dependent manner. Dobutamine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 12818968-7 2003 Salbutamol had a similar suppressive effect on LPS-stimulated MIP-1alpha and IL-8 production. Albuterol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 12818968-10 2003 These findings suggest that dobutamine may inhibit macrophage chemotaxis, as well as MIP-1alpha and IL-8 production by monocytes. Dobutamine 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 14506934-5 2003 RESULTS: Treatment of granulosa-lutein cells with of IL-1alpha (1 nM), TNF-alpha (1 nM), TPA (1 nM) and db-cAMP (100 microM) produced higher levels of IL-8 than untreated cells by 8 hr (2274.7 +/- 146.3, 1489.8 +/- 190.1, 1452.9 +/- 152.7, 1313.6 +/- 48.4 pg/mL, respectively; control = 457.7 +/- 38.2 pg/mL; P < 0.001). db-cAMP 104-111 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 12818968-13 2003 Our study suggests that dobutamine may inhibit macrophage chemotaxis, as well as lipopolysaccharide-induced MIP-1alpha and IL-8 production by human monocytes. Dobutamine 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). Toluene 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12811578-0 2003 Comparative effects of polyphenols from green tea (EGCG) and soybean (genistein) on VEGF and IL-8 release from normal human keratinocytes stimulated with the proinflammatory cytokine TNFalpha. epigallocatechin gallate 51-55 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 12811578-3 2003 We therefore evaluated the effects of green tea, its major component epigallocatechin-3-gallate (EGCG) and an isoflavone derived from soybean (genistein) on the release of VEGF and IL-8 by activated normal human keratinocytes (NHK). epigallocatechin gallate 69-95 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). Toluene 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12811578-3 2003 We therefore evaluated the effects of green tea, its major component epigallocatechin-3-gallate (EGCG) and an isoflavone derived from soybean (genistein) on the release of VEGF and IL-8 by activated normal human keratinocytes (NHK). epigallocatechin gallate 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). Toluene 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12811578-3 2003 We therefore evaluated the effects of green tea, its major component epigallocatechin-3-gallate (EGCG) and an isoflavone derived from soybean (genistein) on the release of VEGF and IL-8 by activated normal human keratinocytes (NHK). Isoflavones 110-120 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 12811578-3 2003 We therefore evaluated the effects of green tea, its major component epigallocatechin-3-gallate (EGCG) and an isoflavone derived from soybean (genistein) on the release of VEGF and IL-8 by activated normal human keratinocytes (NHK). Genistein 143-152 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). Xylenes 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12811578-8 2003 Green tea and EGCG were also potent inhibitors of IL-8 release by TNFalpha-stimulated NHK, whereas genistein exerted only minor effects. epigallocatechin gallate 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). Xylenes 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12811578-9 2003 These results underline the divergent pathways involved in the downregulation of VEGF and IL-8 by polyphenols in activated keratinocytes. Polyphenols 98-109 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). Xylenes 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). pseudocumene 89-105 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12672669-0 2003 Progesterone represses interleukin-8 and cyclo-oxygenase-2 in human lower segment fibroblast cells and amnion epithelial cells. Progesterone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). pseudocumene 89-105 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). pseudocumene 89-105 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). phenylcyclohexane 107-124 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). phenylcyclohexane 107-124 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). phenylcyclohexane 107-124 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). 2,6-dimethylnaphthalene 129-148 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). 2,6-dimethylnaphthalene 129-148 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). 2,6-dimethylnaphthalene 129-148 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). phenylcyclohexane 288-305 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). phenylcyclohexane 288-305 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). phenylcyclohexane 288-305 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). 2,6-dimethylnaphthalene 310-329 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). 2,6-dimethylnaphthalene 310-329 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12871843-13 2003 Furthermore, GM-CSF, RANTES and to a lesser extent IL-8 release from HASMC treated with TNFalpha and IL-1beta was inhibited dosedependently by SP600125. hasmc 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 12851741-6 2003 There was a dose-related differential response in IL-8 release at 24 h. Toluene, xylene, trimethylbenzene, cyclohexylbenzene and dimethylnaphthalene significantly decreased IL-8 release at the respective HNTDs, while IL-8 release did not continue to decrease, or significantly increased (cyclohexylbenzene and dimethylnaphthalene), at the LD(50). 2,6-dimethylnaphthalene 310-329 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12871843-13 2003 Furthermore, GM-CSF, RANTES and to a lesser extent IL-8 release from HASMC treated with TNFalpha and IL-1beta was inhibited dosedependently by SP600125. pyrazolanthrone 143-151 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 12851741-7 2003 IL-8 significantly increased with both doses of methylnaphthalene and naphthalene. 1-methylnaphthalene 48-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12851741-7 2003 IL-8 significantly increased with both doses of methylnaphthalene and naphthalene. naphthalene 54-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12901850-2 2003 We have observed that nitrosoglutathione or another NO-generating compound spermine NONOate caused significant accumulation of IL-8 mRNA. S-Nitrosoglutathione 22-40 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 12839933-9 2003 Treatment with the proteasome inhibitor, MG-132, blocked BBS-stimulated NF kappa B DNA binding, and IL-8 and VEGF expression and secretion. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 41-47 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 12901850-5 2003 Furthermore, we have shown that IL-8 induction was not inhibited by catalase and the iron chelator deferoxamine, indicating that the inhibitory actions of DMSO and DMTU are not related to scavenging of reactive oxygen species produced from hydrogen peroxide in the iron-catalyzed reactions. Dimethyl Sulfoxide 155-159 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 12791215-2 2003 Histamine, released from the conjunctival mast cells, might stimulate the synthesis of proinflammatory molecules such as IL-6 and IL-8 by the epithelial cells through the receptors that couple to inositol phosphate generation and, therefore, amplify the allergic response. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 12901850-2 2003 We have observed that nitrosoglutathione or another NO-generating compound spermine NONOate caused significant accumulation of IL-8 mRNA. spermine nitric oxide complex 75-91 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 12791215-2 2003 Histamine, released from the conjunctival mast cells, might stimulate the synthesis of proinflammatory molecules such as IL-6 and IL-8 by the epithelial cells through the receptors that couple to inositol phosphate generation and, therefore, amplify the allergic response. Inositol Phosphates 196-214 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 12901850-5 2003 Furthermore, we have shown that IL-8 induction was not inhibited by catalase and the iron chelator deferoxamine, indicating that the inhibitory actions of DMSO and DMTU are not related to scavenging of reactive oxygen species produced from hydrogen peroxide in the iron-catalyzed reactions. 1,3-dimethyl-4-thiouracil 164-168 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 12901850-3 2003 Pretreatment of cells with pyrrolidine dithiocarbamate or with antioxidants, which scavenge hydroxyl radical, dimethyl sulfoxide (DMSO), or dimetylthiourea (DMTU) completely abrogated NO-dependent induction of IL-8 gene expression. pyrrolidine dithiocarbamic acid 27-54 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 12901850-7 2003 Therefore, it seems likely that in U937 cells, hydroxyl radicals or species with reactivity similar to hydroxyl radicals contribute to NO-mediated IL-8 gene induction. Hydroxyl Radical 47-64 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 12901850-7 2003 Therefore, it seems likely that in U937 cells, hydroxyl radicals or species with reactivity similar to hydroxyl radicals contribute to NO-mediated IL-8 gene induction. Hydroxyl Radical 103-120 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 12901850-4 2003 The transcriptional activation of IL-8 gene was not affected by sodium formate or sodium salicylate, suggesting that suppression of the IL-8 gene induction is specific to the class of hydroxyl radical scavenger used. Hydroxyl Radical 184-200 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 12901850-4 2003 The transcriptional activation of IL-8 gene was not affected by sodium formate or sodium salicylate, suggesting that suppression of the IL-8 gene induction is specific to the class of hydroxyl radical scavenger used. Hydroxyl Radical 184-200 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 12882457-5 2003 IL-6 and IL-8 production was lower in COPD patients taking inhaled steroids. Steroids 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 12882461-9 2003 These data suggest that regular use of salbutamol can augment airway CXCL8/interleukin-8 responses to allergen challenge and that this CXCL8/interleukin-8 could contribute to the airway inflammatory response. Albuterol 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 69-74 12882461-0 2003 Regular salbutamol use increases CXCL8 responses in asthma: relationship to the eosinophil response. Albuterol 8-18 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 12882461-9 2003 These data suggest that regular use of salbutamol can augment airway CXCL8/interleukin-8 responses to allergen challenge and that this CXCL8/interleukin-8 could contribute to the airway inflammatory response. Albuterol 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 75-88 12882461-9 2003 These data suggest that regular use of salbutamol can augment airway CXCL8/interleukin-8 responses to allergen challenge and that this CXCL8/interleukin-8 could contribute to the airway inflammatory response. Albuterol 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 141-154 12899430-2 2003 An expert witness for the defence alleged that a deficient volume of blood in the tube sent for analysis meant an excess amount of sodium fluoride (NaF) preservative, which would increase the concentration of ethanol, determined by headspace gas chromatography (HS-GC), owing to a salting-out effect. Sodium Fluoride 131-146 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 14979118-0 2003 [Determination of interleukin-8 in induced sputum of workers exposed to low concentrations of asbestos]. Asbestos 94-102 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 12899430-2 2003 An expert witness for the defence alleged that a deficient volume of blood in the tube sent for analysis meant an excess amount of sodium fluoride (NaF) preservative, which would increase the concentration of ethanol, determined by headspace gas chromatography (HS-GC), owing to a salting-out effect. Ethanol 209-216 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 12899430-2 2003 An expert witness for the defence alleged that a deficient volume of blood in the tube sent for analysis meant an excess amount of sodium fluoride (NaF) preservative, which would increase the concentration of ethanol, determined by headspace gas chromatography (HS-GC), owing to a salting-out effect. hs-gc 262-267 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 12899430-8 2003 Our experiments showed that a deficient volume of blood and excess NaF actually lowered the concentration of ethanol by 2-3% compared with heparinised blood. Ethanol 109-116 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 12794155-4 2003 The tyrosine kinase inhibitor herbimycin blocked Ad19-induced IL-8 expression. herbimycin 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 14518569-8 2003 15d-PGJ2 induced, by itself, the expression of interleukin-8, a potent proinflammatory chemokine, in HUVEC. 15-deoxy-delta(12,14)-prostaglandin J2 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 12837459-10 2003 A reduction in urinary IL-8 levels after treatment with bacille Calmette-Guerin or mitomycin C may reflect a decrease in bladder cancer cells and/or in other cells that produce IL-8. Mitomycin 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 12837459-10 2003 A reduction in urinary IL-8 levels after treatment with bacille Calmette-Guerin or mitomycin C may reflect a decrease in bladder cancer cells and/or in other cells that produce IL-8. Mitomycin 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 12818188-7 2003 Moreover, human hepatic cathepsin L cleaved 77IL-8 between Arg(5) and Ser(6), which is the same cleavage site as the putative converting enzyme, resulting in 72IL-8 formation. Arginine 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 12818188-7 2003 Moreover, human hepatic cathepsin L cleaved 77IL-8 between Arg(5) and Ser(6), which is the same cleavage site as the putative converting enzyme, resulting in 72IL-8 formation. Serine 70-73 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 12794155-6 2003 Respective inhibitors of these kinases, PP2 and PD98059, also blocked Ad19-induced IL-8 mRNA and protein expression. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 12749935-2 2003 Based on the results of an in vitro transmigration system, human recombinant interleukin-8 (rhIL-8; 1.25 microg per mare and 5 microg per cow in 50 ml phosphate-buffered saline) was used to attract polymorphonuclear neutrophil granulocytes (PMNs) into the uteri. Phosphate-Buffered Saline 151-176 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 12842763-11 2003 These results indicate that methylprednisolone significantly reduces the production of IL-8 in an isolated CPB system. Methylprednisolone 28-46 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 12600836-5 2003 Furthermore, the PKR inhibitor 2-aminopurine significantly blocked dsRNA-induced RANTES and IL-8 secretion, whereas the p38 mitogen-activated protein kinase inhibitor SB203580 suppressed dsRNA-induced IL-8, but not RANTES. 2-Aminopurine 31-44 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 12600836-5 2003 Furthermore, the PKR inhibitor 2-aminopurine significantly blocked dsRNA-induced RANTES and IL-8 secretion, whereas the p38 mitogen-activated protein kinase inhibitor SB203580 suppressed dsRNA-induced IL-8, but not RANTES. SB 203580 167-175 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 12809941-0 2003 Interleukin 8 response and oxidative stress in HepG2 cells treated with ethanol, acetaldehyde or lipopolysaccharide. Ethanol 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 12797494-0 2003 Possible anti-inflammatory effect of salmeterol against interleukin-8 and neutrophil activation in asthma in vivo. Salmeterol Xinafoate 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 12797494-3 2003 There is currently interest in the "neutrophil system" in asthma, and thus the aim of the present study was to investigate the effect of salmeterol on interleukin (IL)-8, neutrophils and myeloperoxidase (MPO) in persistent asthma. Salmeterol Xinafoate 137-147 C-X-C motif chemokine ligand 8 Homo sapiens 151-169 12797494-10 2003 In contrast, introducing salmeterol significantly reduced IL-8 and MPO levels, but did not affect BALF neutrophil numbers. Salmeterol Xinafoate 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12809941-0 2003 Interleukin 8 response and oxidative stress in HepG2 cells treated with ethanol, acetaldehyde or lipopolysaccharide. Acetaldehyde 81-93 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 12809941-1 2003 The aim of this work was to study the induction and secretion of interleukin 8 (IL-8) and some oxidative stress parameters after ethanol (EtOH), acetaldehyde (Ac) or lipopolysaccharide (LPS) treatment on HepG2 cells. Ethanol 129-136 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 12809941-1 2003 The aim of this work was to study the induction and secretion of interleukin 8 (IL-8) and some oxidative stress parameters after ethanol (EtOH), acetaldehyde (Ac) or lipopolysaccharide (LPS) treatment on HepG2 cells. Ethanol 129-136 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 12809941-1 2003 The aim of this work was to study the induction and secretion of interleukin 8 (IL-8) and some oxidative stress parameters after ethanol (EtOH), acetaldehyde (Ac) or lipopolysaccharide (LPS) treatment on HepG2 cells. Ethanol 138-142 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 12875365-0 2003 Combined effect of hydrogen peroxide induced oxidative stress and IL-1 alpha on IL-8 production in CaCo-2 cells (a human colon carcinoma cell line) and normal intestinal epithelial cells. Hydrogen Peroxide 19-36 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 12875365-2 2003 We examined the IL-8 response after brief exposure to hydrogen peroxide induced oxidative stress in CaCo-2 cells (a human colon carcinoma cell line) and in human intestinal epithelial cells. Hydrogen Peroxide 54-71 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 12875365-4 2003 A transient up-regulation of IL-8 mRNA expression was observed after hydrogen peroxide treatment. Hydrogen Peroxide 69-86 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 12875365-5 2003 Hydrogen peroxide induced oxidative stress was also observed to promote IL-8 secretion. Hydrogen Peroxide 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 12809941-1 2003 The aim of this work was to study the induction and secretion of interleukin 8 (IL-8) and some oxidative stress parameters after ethanol (EtOH), acetaldehyde (Ac) or lipopolysaccharide (LPS) treatment on HepG2 cells. Acetaldehyde 145-157 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 12875365-6 2003 Exposure to hydrogen peroxide, followed by IL-1alpha, enhanced IL-8 production over that achieved with IL-1alpha alone. Hydrogen Peroxide 12-29 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 12809941-1 2003 The aim of this work was to study the induction and secretion of interleukin 8 (IL-8) and some oxidative stress parameters after ethanol (EtOH), acetaldehyde (Ac) or lipopolysaccharide (LPS) treatment on HepG2 cells. Acetaldehyde 145-157 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 12875367-0 2003 Alveolar epithelial cell-macrophage interactions affect oxygen-stimulated interleukin-8 release. Oxygen 56-62 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 12809941-1 2003 The aim of this work was to study the induction and secretion of interleukin 8 (IL-8) and some oxidative stress parameters after ethanol (EtOH), acetaldehyde (Ac) or lipopolysaccharide (LPS) treatment on HepG2 cells. Acetaldehyde 159-161 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 12809941-1 2003 The aim of this work was to study the induction and secretion of interleukin 8 (IL-8) and some oxidative stress parameters after ethanol (EtOH), acetaldehyde (Ac) or lipopolysaccharide (LPS) treatment on HepG2 cells. Acetaldehyde 159-161 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 12809941-15 2003 This observation suggests that in the in vivo liver, the mechanism of ethanol-induced IL-8 production requires ethanol metabolism, and hepatocytes do not require the interaction among different populations of liver cells to respond. Ethanol 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12781700-6 2003 However, this effect of BFA was less marked when neutrophils were treated with dexamethasone, interleukin-8 (IL-8), or dibutyryl cAMP (dbcAMP). Brefeldin A 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 12781700-6 2003 However, this effect of BFA was less marked when neutrophils were treated with dexamethasone, interleukin-8 (IL-8), or dibutyryl cAMP (dbcAMP). Brefeldin A 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 12809941-15 2003 This observation suggests that in the in vivo liver, the mechanism of ethanol-induced IL-8 production requires ethanol metabolism, and hepatocytes do not require the interaction among different populations of liver cells to respond. Ethanol 111-118 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12765200-0 2003 Suppression of IL-8 gene transcription by resveratrol in phorbol ester treated human monocytic cells. Resveratrol 42-53 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 12765200-10 2003 Resveratrol could inhibit PMA-induced IL-8 production in U937 cells at protein and mRNA levels. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 12765200-10 2003 Resveratrol could inhibit PMA-induced IL-8 production in U937 cells at protein and mRNA levels. Tetradecanoylphorbol Acetate 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 12765200-0 2003 Suppression of IL-8 gene transcription by resveratrol in phorbol ester treated human monocytic cells. Phorbol Esters 57-70 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 12765200-11 2003 The suppression of IL-8 gene transcription by resveratrol was, at least partly, due to inhibition of AP-1 activation. Resveratrol 46-57 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 12765200-2 2003 To observe the modulation of interleukin-8 (IL-8) production in human monocytic cells by resveratrol and explore its mechanism at the gene transcription level, U937 cells were stimulated with phorbol 12-myristate 13-acetate (PMA) for 24h. Resveratrol 89-100 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 12765200-2 2003 To observe the modulation of interleukin-8 (IL-8) production in human monocytic cells by resveratrol and explore its mechanism at the gene transcription level, U937 cells were stimulated with phorbol 12-myristate 13-acetate (PMA) for 24h. Resveratrol 89-100 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 12765200-7 2003 0.01-100 nM PMA could significantly induce IL-8 production in U937 cells; 10 microM Dexamethasone and 10, 1, 0.1 microM resveratrol could inhibit PMA-induced IL-8 protein production and mRNA accumulation. Tetradecanoylphorbol Acetate 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 12765200-7 2003 0.01-100 nM PMA could significantly induce IL-8 production in U937 cells; 10 microM Dexamethasone and 10, 1, 0.1 microM resveratrol could inhibit PMA-induced IL-8 protein production and mRNA accumulation. Tetradecanoylphorbol Acetate 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 12765200-7 2003 0.01-100 nM PMA could significantly induce IL-8 production in U937 cells; 10 microM Dexamethasone and 10, 1, 0.1 microM resveratrol could inhibit PMA-induced IL-8 protein production and mRNA accumulation. Dexamethasone 84-97 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 12765200-7 2003 0.01-100 nM PMA could significantly induce IL-8 production in U937 cells; 10 microM Dexamethasone and 10, 1, 0.1 microM resveratrol could inhibit PMA-induced IL-8 protein production and mRNA accumulation. Resveratrol 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 12765200-7 2003 0.01-100 nM PMA could significantly induce IL-8 production in U937 cells; 10 microM Dexamethasone and 10, 1, 0.1 microM resveratrol could inhibit PMA-induced IL-8 protein production and mRNA accumulation. Resveratrol 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 12765200-7 2003 0.01-100 nM PMA could significantly induce IL-8 production in U937 cells; 10 microM Dexamethasone and 10, 1, 0.1 microM resveratrol could inhibit PMA-induced IL-8 protein production and mRNA accumulation. Tetradecanoylphorbol Acetate 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 12765200-7 2003 0.01-100 nM PMA could significantly induce IL-8 production in U937 cells; 10 microM Dexamethasone and 10, 1, 0.1 microM resveratrol could inhibit PMA-induced IL-8 protein production and mRNA accumulation. Tetradecanoylphorbol Acetate 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 12759450-3 2003 Transient transfection with the constitutively active catalytic subunit of PKC delta (PKC delta-CAT), and treatment with bryostatin 1, an activator of PKC delta, each increased transcription from the IL-8 promoter, whereas overexpression of PKC epsilon had minor effects. bryostatin 1 121-133 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 12759450-4 2003 Expression of a dominant negative PKC delta mutant (PKC delta-KR) or pretreatment of cells with rottlerin, a chemical PKC delta inhibitor, attenuated TNF-alpha- and phorbol ester-induced transcription from the IL-8 promoter. rottlerin 96-105 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 12759450-4 2003 Expression of a dominant negative PKC delta mutant (PKC delta-KR) or pretreatment of cells with rottlerin, a chemical PKC delta inhibitor, attenuated TNF-alpha- and phorbol ester-induced transcription from the IL-8 promoter. Phorbol Esters 165-178 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 12759450-5 2003 Bryostatin 1 treatment increased IL-8 protein abundance in primary airway epithelial cells. bryostatin 1 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 12856595-6 2003 The results showed that NF-kappa B p65 antisense oligonucleotides resulted in down-regulation of NF-kappa B p65 expression, blocked the expression of IL-1 beta mRNA and IL-8 mRNA, and strikingly reduced the production of IL-1 beta and IL-8, and these effects were greater than those of dexamethasone in cultured LPMC from patients with UC(P < 0.05). Dexamethasone 286-299 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 12856595-6 2003 The results showed that NF-kappa B p65 antisense oligonucleotides resulted in down-regulation of NF-kappa B p65 expression, blocked the expression of IL-1 beta mRNA and IL-8 mRNA, and strikingly reduced the production of IL-1 beta and IL-8, and these effects were greater than those of dexamethasone in cultured LPMC from patients with UC(P < 0.05). Oligonucleotides 49-65 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 12856595-6 2003 The results showed that NF-kappa B p65 antisense oligonucleotides resulted in down-regulation of NF-kappa B p65 expression, blocked the expression of IL-1 beta mRNA and IL-8 mRNA, and strikingly reduced the production of IL-1 beta and IL-8, and these effects were greater than those of dexamethasone in cultured LPMC from patients with UC(P < 0.05). Oligonucleotides 49-65 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 12857601-7 2003 The p38 mitogen-activated protein kinase inhibitor SB 203580 inhibits the IL-8 mRNA expression and the release of protein from neutrophils. SB 203580 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 12857601-8 2003 The release of IL-8 from SAA-stimulated neutrophils is strongly suppressed by the addition of N-acetyl-l-cysteine, alpha-mercaptoethanol, glutathione, and dexamethasone. Acetylcysteine 94-113 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 12857601-8 2003 The release of IL-8 from SAA-stimulated neutrophils is strongly suppressed by the addition of N-acetyl-l-cysteine, alpha-mercaptoethanol, glutathione, and dexamethasone. alpha-mercaptoethanol 115-136 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 12857601-8 2003 The release of IL-8 from SAA-stimulated neutrophils is strongly suppressed by the addition of N-acetyl-l-cysteine, alpha-mercaptoethanol, glutathione, and dexamethasone. Glutathione 138-149 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 12857601-8 2003 The release of IL-8 from SAA-stimulated neutrophils is strongly suppressed by the addition of N-acetyl-l-cysteine, alpha-mercaptoethanol, glutathione, and dexamethasone. Dexamethasone 155-168 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 12856595-6 2003 The results showed that NF-kappa B p65 antisense oligonucleotides resulted in down-regulation of NF-kappa B p65 expression, blocked the expression of IL-1 beta mRNA and IL-8 mRNA, and strikingly reduced the production of IL-1 beta and IL-8, and these effects were greater than those of dexamethasone in cultured LPMC from patients with UC(P < 0.05). lpmc 312-316 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 12637525-9 2003 Our data demonstrate that the cyclic stretch of HASMC causes the increased production of IL-8 by activating the AP-1 and C/EBP transcription factors through the activation of ERK1/2 and p38 kinase signaling pathways. hasmc 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 12793907-3 2003 We recently reported that plasma IL-8 is increased in obese subjects with normal glucose tolerance (NGT). Glucose 81-88 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 12793907-12 2003 CONCLUSION: Plasma IL-8 concentrations after glucose load are increased in obese IGT subjects in comparison to normoglycemic weight-matched individuals. Glucose 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 12793907-13 2003 Increase in plasma IL-8 might be both insulin-mediated (during clamp) and glucose-mediated (during OGTT). Glucose 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 12639714-0 2003 Interleukin-8 production induced by the endozepine triakontatetraneuropeptide in human neutrophils: role of calcium and pharmacological investigation of signal transduction pathways. Calcium 108-115 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 12754109-8 2003 Relative and competitive RT-PCR analysis verified downregulation of TNFalpha-mediated expression of CD40L and IL-8 by Dexa and Dexa-Ab(hEsel), respectively. Dexamethasone 118-122 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 12754109-8 2003 Relative and competitive RT-PCR analysis verified downregulation of TNFalpha-mediated expression of CD40L and IL-8 by Dexa and Dexa-Ab(hEsel), respectively. dexa-ab 127-134 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 12770938-8 2003 5 When EC were preincubated with the specific Rho kinase (ROCK) inhibitor Y-27632, we observed a reduction in PMN adherence in response to thrombin, as well as a decrease in thrombin-stimulated IL-8 production. Y 27632 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 12727366-6 2003 Prolonged incubation of both serum-opsonized and -unopsonized zymosan particles with HUVEC induced increased secretion of the proinflammatory cytokines IL-6 and IL-8 to the cell culture supernatants, but had no effect on production of oxygen radicals. Zymosan 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 12736519-3 2003 DFX significantly increased interleukin (IL)-6, IL-8, and tumor necrosis factor (TNF)-alpha production compared with the control in a time-dependent manner (p<0.05), but did not affect IL-1alpha production and mRNA expression. Deferoxamine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 12639714-2 2003 Because interleukin-8 (IL-8) production is Ca(2+) dependent and can be induced by chemotactic stimuli, we have investigated the ability of TTN to induce IL-8 production in PMNs, as well as the signal transduction mechanisms involved. Tartronic acid 139-142 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 12736467-0 2003 Inhibitory effect of TNF-alpha and IL-8 secretion by pimarane-type diterpenoids from Acanthopanax koreanum. pimarane 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 12639714-3 2003 Our results show that TTN increases IL-8 release and IL-8 mRNA expression in a concentration- and time-dependent fashion, and these effects are prevented by the Ca(2+) chelator BAPTA-AM. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 177-185 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 12736467-0 2003 Inhibitory effect of TNF-alpha and IL-8 secretion by pimarane-type diterpenoids from Acanthopanax koreanum. Diterpenes 67-79 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 12639714-3 2003 Our results show that TTN increases IL-8 release and IL-8 mRNA expression in a concentration- and time-dependent fashion, and these effects are prevented by the Ca(2+) chelator BAPTA-AM. 1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester 177-185 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 12736467-2 2003 Acanthoic acid was isolated in high yields and showed potent inhibitory activity on the IL-8 secretion of the TNF-alpha-stimulated human colon adenocarcinoma cell line HT-29 and on the TNF-alpha secretion of the trypsin-stimulated human leukemic mast cell line HMC-1. acanthoic acid 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12639714-4 2003 TTN-induced [Ca(2+)](i) changes and IL-8 mRNA expression are sensitive to pertussis toxin, to the phospholipase C (PLC) inhibitor U73122 (but not to its inactive analogue U73343) and to the protein kinase C (PKC) inhibitor calphostin C. Tartronic acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 12639714-4 2003 TTN-induced [Ca(2+)](i) changes and IL-8 mRNA expression are sensitive to pertussis toxin, to the phospholipase C (PLC) inhibitor U73122 (but not to its inactive analogue U73343) and to the protein kinase C (PKC) inhibitor calphostin C. 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 130-136 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 12639714-5 2003 It is therefore suggested that TTN-induced IL-8 production in human PMNs results from a G protein-operated, PLC-activated [Ca(2+)](i) rise, and PKC contributes to this effect. Tartronic acid 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 12849706-0 2003 Glutamine decreases lipopolysaccharide-induced IL-8 production in Caco-2 cells through a non-NF-kappaB p50 mechanism. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12849706-10 2003 The addition of Gln (0.5 or 5.0mM) decreased IL-8 peptide and mRNA expression. Glutamine 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 12849706-13 2003 These results indicate that the lack of glutamine increases IL-8 production by Caco-2 cells after LPS stimulation. Glutamine 40-49 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 12849706-8 2003 The largest amount of IL-8 was secreted by cells in the presence of MS with no Gln in the medium after exposure to LPS. Glutamine 79-82 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 12849706-14 2003 However, the glutamine-mediated decrease in LPS-stimulated IL-8 production is not associated with NF-kappaB p50 nuclear binding. Glutamine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 12880368-1 2003 The stimulatory effects of sodium fluoride (NaF) on bone formation have been explained solely by its activation of osteoblasts. Sodium Fluoride 27-42 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 12697421-5 2003 The induced IL-8 and MCP-1 proteins were almost completely supporessed by U0126, a specific mitogen-activated protein kinase kinase (MEK) inhibitor, or by SB203580, a selective p38 inhibitor. U 0126 74-79 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 12697421-5 2003 The induced IL-8 and MCP-1 proteins were almost completely supporessed by U0126, a specific mitogen-activated protein kinase kinase (MEK) inhibitor, or by SB203580, a selective p38 inhibitor. SB 203580 155-163 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 12697421-7 2003 Induction of IL-8 and MCP-1 was abrogated by Ro318220, an inhibitor of PKC, as well as by genistein or herbimycin A, inhibitors of PTK. Ro 31-8220 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 12697421-7 2003 Induction of IL-8 and MCP-1 was abrogated by Ro318220, an inhibitor of PKC, as well as by genistein or herbimycin A, inhibitors of PTK. Genistein 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 12697421-7 2003 Induction of IL-8 and MCP-1 was abrogated by Ro318220, an inhibitor of PKC, as well as by genistein or herbimycin A, inhibitors of PTK. herbimycin 103-115 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 12717385-11 2003 LPS-induced IL-8 secretion is completely inhibited by the IkappaB super repressor (Ad5IkappaB) and partially inhibited by a specific JNK inhibitor, SP600125. pyrazolanthrone 148-156 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 12880368-5 2003 NaF at subtoxic concentrations (<0.5 mM) significantly up-regulated activities of several intracellular enzymes (lactate dehydrogenase, beta-glucuronidase, acid phosphatase), cellular reduction of nitroblue tetrazolium, and nitric oxide (NO) production; which are all accepted as general differentiation markers. Nitroblue Tetrazolium 200-221 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 12880368-5 2003 NaF at subtoxic concentrations (<0.5 mM) significantly up-regulated activities of several intracellular enzymes (lactate dehydrogenase, beta-glucuronidase, acid phosphatase), cellular reduction of nitroblue tetrazolium, and nitric oxide (NO) production; which are all accepted as general differentiation markers. Nitric Oxide 227-239 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 12533503-9 2003 The increase in mRNA (fold difference from preexercise) was attenuated in CHO (15.9-fold) compared with Pla (35.2-fold) for IL-6 (P = 0.071) and IL-8 (CHO, 7.8-fold; Pla, 23.3-fold; P = 0.063). CAV protocol 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 12533503-9 2003 The increase in mRNA (fold difference from preexercise) was attenuated in CHO (15.9-fold) compared with Pla (35.2-fold) for IL-6 (P = 0.071) and IL-8 (CHO, 7.8-fold; Pla, 23.3-fold; P = 0.063). CAV protocol 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 12533503-10 2003 CHO compared with Pla beverage ingestion attenuates the increase in plasma IL-6, IL-10, and IL-1ra and gene expression for IL-6 and IL-8 in athletes running 3 h at 70% Vo(2 max) despite no differences in muscle glycogen content. CAV protocol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 12713595-8 2003 DP treatment also blocked VCAM-1 induction in human umbilical vein endothelium and blocked induction of a host of NF-kB activated genes in HDMEC including ICAM-1, IL-8, and tissue factor. 2,2'-Dipyridyl 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 12695526-9 2003 In addition, we show that AJA inhibits interleukin-8 promoter activity in a PPARgamma-dependent manner, suggesting a link between the anti-inflammatory action of AJA and the activation of PPARgamma. lenabasum 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 12871375-0 2003 The promoting effect of epinephrine on lipopolysaccharide-induced interleukin-8 production in whole blood may be mediated by thromboxane A2. Epinephrine 24-35 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 12871375-0 2003 The promoting effect of epinephrine on lipopolysaccharide-induced interleukin-8 production in whole blood may be mediated by thromboxane A2. Thromboxane A2 125-139 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 12871375-1 2003 Epinephrine is known to enhance lipopolysaccharide (LPS)-induced interleukin (IL)-8 secretion in a platelet dependent manner. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 65-83 12871375-3 2003 ASA ingestion significantly (global P < 0.05) reduced the enhancing effect of epinephrine on LPS-induced IL-8 release by 15-28%. Aspirin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 12871375-3 2003 ASA ingestion significantly (global P < 0.05) reduced the enhancing effect of epinephrine on LPS-induced IL-8 release by 15-28%. Epinephrine 81-92 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 12871375-5 2003 U46619 mimicked the epinephrine effect: 20 ng mL(-1) U46619 enhanced LPS-induced IL-8 release by 39% (P < 0.05). Epinephrine 20-31 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 12871375-6 2003 Furthermore, preincubation of whole blood with 75 micro mol L-1 or 150 micromol L(-1) SQ29548, a TxA2 receptor antagonist, completely blocked epinephrine"s promoting effect on LPS-induced IL-8 release. Epinephrine 142-153 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 12695526-9 2003 In addition, we show that AJA inhibits interleukin-8 promoter activity in a PPARgamma-dependent manner, suggesting a link between the anti-inflammatory action of AJA and the activation of PPARgamma. lenabasum 162-165 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 12753408-0 2003 Regulation of 1-alpha, 25-dihydroxyvitamin D3 on interleukin-6 and interleukin-8 induced by sulfur mustard (HD) on human skin cells. Calcitriol 14-45 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 12753408-0 2003 Regulation of 1-alpha, 25-dihydroxyvitamin D3 on interleukin-6 and interleukin-8 induced by sulfur mustard (HD) on human skin cells. Mustard Gas 92-106 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 12456400-6 2003 We also observed that the expression of myc-LXA(4) conferred enhanced downregulation of IL-8 expression in response to LXA(4) analog and that blockade of the CysLT1 receptor by montelukast did not prevent this response to LXA(4) analog. N-(1H-benzimidazol-2-ylmethyl)-2-methoxyacetamide 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12938820-15 2003 Mesothelial cells showed a twofold increase in interleukin (IL)-6 and IL-8 production after exposure to 3-DG. 3-deoxyglucosone 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 12938820-18 2003 Upon short exposure to a single GDP, MCs react with enhanced cytotoxic damage and a proinflammatory response, evidenced by increased VCAM-1 expression and elevated production of IL-6 and IL-8. Guanosine Diphosphate 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 12938820-18 2003 Upon short exposure to a single GDP, MCs react with enhanced cytotoxic damage and a proinflammatory response, evidenced by increased VCAM-1 expression and elevated production of IL-6 and IL-8. mcs 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 12706459-2 2003 In the present study, we determined that Caco-2 cells express the kappa-opioid receptor and its activation by trans-(+/-)-3,4-dichloro-N-methyl-N[2-(1-pyrolidinyl)cyclohexyl]benzeneacetamide methanesulfonate (U-50488) leads to decreased interleukin-8 secretion in the presence of interleukin-1beta. trans-(+/-)-3,4-dichloro-n-methyl-n[2-(1-pyrolidinyl)cyclohexyl]benzeneacetamide methanesulfonate 110-207 C-X-C motif chemokine ligand 8 Homo sapiens 237-250 12456400-6 2003 We also observed that the expression of myc-LXA(4) conferred enhanced downregulation of IL-8 expression in response to LXA(4) analog and that blockade of the CysLT1 receptor by montelukast did not prevent this response to LXA(4) analog. N-(1H-benzimidazol-2-ylmethyl)-2-methoxyacetamide 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12495941-4 2003 Pretreatment with the protein tyrosine kinase-specific inhibitors genistein and herbimycin A effectively blocked LPS-induced NF-kappaB activation as well as IL-8 gene expression in human peripheral blood monocytes. Genistein 66-75 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 12495941-7 2003 These findings provide evidence that LPS-induced NF-kappaB activation and IL-8 gene expression use a signaling pathway requiring protein tyrosine kinase and that such regulation may occur through tyrosine phosphorylation of TLR4. Tyrosine 137-145 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 12711624-7 2003 Release of IL-8 was triggered by UDP, ATP, alpha,beta-meATP and BzATP, but not by UTP or ADP. Uridine Diphosphate 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 12653788-7 2003 The correlation analysis revealed a significant correlation of IL-6 and/or IL-8 to age, total fructose, immunoglobulin G (IgG) concentration and leucocyte count. Fructose 94-102 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 12654635-0 2003 Binding of interleukin-8 to heparan sulfate and chondroitin sulfate in lung tissue. Heparitin Sulfate 28-43 C-X-C motif chemokine ligand 8 Homo sapiens 11-24 12654635-0 2003 Binding of interleukin-8 to heparan sulfate and chondroitin sulfate in lung tissue. Chondroitin Sulfates 48-67 C-X-C motif chemokine ligand 8 Homo sapiens 11-24 12654635-5 2003 Confocal microscopy demonstrated IL-8 binding to specific anatomic locations such as cell surfaces and extracellular matrix that were enriched with heparan sulfate and chondroitin sulfate. Heparitin Sulfate 148-163 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 12654635-5 2003 Confocal microscopy demonstrated IL-8 binding to specific anatomic locations such as cell surfaces and extracellular matrix that were enriched with heparan sulfate and chondroitin sulfate. Chondroitin Sulfates 168-187 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 12654635-6 2003 Removal of heparan sulfate or chondroitin sulfate from lung tissue significantly decreased the binding of 125I-IL-8. Heparitin Sulfate 11-26 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 12654635-6 2003 Removal of heparan sulfate or chondroitin sulfate from lung tissue significantly decreased the binding of 125I-IL-8. Chondroitin Sulfates 30-49 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 12654635-9 2003 These findings suggest that IL-8-glycosaminoglycan interactions determine the location where IL-8 binds in lung tissue and provides a site for the dimerization of IL-8, which increases the local concentration of IL-8 in the lungs. Glycosaminoglycans 33-50 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 12654635-9 2003 These findings suggest that IL-8-glycosaminoglycan interactions determine the location where IL-8 binds in lung tissue and provides a site for the dimerization of IL-8, which increases the local concentration of IL-8 in the lungs. Glycosaminoglycans 33-50 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 12654635-9 2003 These findings suggest that IL-8-glycosaminoglycan interactions determine the location where IL-8 binds in lung tissue and provides a site for the dimerization of IL-8, which increases the local concentration of IL-8 in the lungs. Glycosaminoglycans 33-50 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 12654635-9 2003 These findings suggest that IL-8-glycosaminoglycan interactions determine the location where IL-8 binds in lung tissue and provides a site for the dimerization of IL-8, which increases the local concentration of IL-8 in the lungs. Glycosaminoglycans 33-50 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 12711624-7 2003 Release of IL-8 was triggered by UDP, ATP, alpha,beta-meATP and BzATP, but not by UTP or ADP. Adenosine Triphosphate 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 12711624-7 2003 Release of IL-8 was triggered by UDP, ATP, alpha,beta-meATP and BzATP, but not by UTP or ADP. alpha,beta-methyleneadenosine 5'-triphosphate 43-59 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 12711624-7 2003 Release of IL-8 was triggered by UDP, ATP, alpha,beta-meATP and BzATP, but not by UTP or ADP. BzATP 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 12711624-10 2003 Release of IL-8 stimulated by BzATP was fully blocked by the P2X(7) blocker KN-62, while release triggered by ATP was only partially inhibited. BzATP 30-35 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 12711624-10 2003 Release of IL-8 stimulated by BzATP was fully blocked by the P2X(7) blocker KN-62, while release triggered by ATP was only partially inhibited. Adenosine Triphosphate 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 12711624-11 2003 IL-8 secretion due to UDP was fully insensitive to KN-62 inhibition. Uridine Diphosphate 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12667212-8 2003 Evaluation of IL-8 and MCP-1 RNA messages by reverse transcription-polymerase chain reaction (RT-PCR) revealed that the inhibitory effect of SB 203580 was associated with a reduction in this parameter. SB 203580 141-150 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 12684317-7 2003 Pretreatment of sputum or neutrophils with either an anti-IL-8 antibody or the LTB(4) antagonist, SB 201146, led to a concentration-dependent inhibition of sputum-induced neutrophil chemotaxis, with a maximum suppression (mean +/- SEM) of 29.2 +/- 4.9% (p < 0.001) from baseline by 100 ng/mL of anti-IL-8 antibody, and 45.6 +/- 7% (p < 0.02) by 10 micro mol/L of SB 201146. SB 201146 98-107 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12684317-7 2003 Pretreatment of sputum or neutrophils with either an anti-IL-8 antibody or the LTB(4) antagonist, SB 201146, led to a concentration-dependent inhibition of sputum-induced neutrophil chemotaxis, with a maximum suppression (mean +/- SEM) of 29.2 +/- 4.9% (p < 0.001) from baseline by 100 ng/mL of anti-IL-8 antibody, and 45.6 +/- 7% (p < 0.02) by 10 micro mol/L of SB 201146. SB 201146 98-107 C-X-C motif chemokine ligand 8 Homo sapiens 303-307 12684317-7 2003 Pretreatment of sputum or neutrophils with either an anti-IL-8 antibody or the LTB(4) antagonist, SB 201146, led to a concentration-dependent inhibition of sputum-induced neutrophil chemotaxis, with a maximum suppression (mean +/- SEM) of 29.2 +/- 4.9% (p < 0.001) from baseline by 100 ng/mL of anti-IL-8 antibody, and 45.6 +/- 7% (p < 0.02) by 10 micro mol/L of SB 201146. SB 201146 369-378 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12676602-7 2003 Cytokine production was significantly associated with metal contents of PM1.0: IL-8 correlated with Cr and Mn, and TNF-alpha correlated with Fe and Cr. Chromium 100-102 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 12694767-14 2003 The unique comparison with Pentoxifylline afforded by this study indicates that at the doses studied Pentoxifylline appears to be superior, correlating with a greater inhibition of IL-8 expression. Pentoxifylline 101-115 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 12689664-1 2003 A converting activity was characterized in human diploid fibroblasts, which secrete 72IL-8 and 77IL-8 in treatment with IFN-beta and poly I: poly C. Poly C 141-147 C-X-C motif chemokine ligand 8 Homo sapiens 86-101 12762338-0 2003 Fluticasone reduces IL-6 and IL-8 production of cystic fibrosis bronchial epithelial cells via IKK-beta kinase pathway. Fluticasone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 12667212-5 2003 The production of IL-8 and monocyte chemotactic protein 1 (MCP-1) was attenuated by 50% when these cells were preincubated with the p38 MAPK inhibitor, SB 203580. SB 203580 152-161 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 12723089-4 2003 All muscles treated with NaC and NaF showed the highest pH and glycogen content (P < 0.05), indicating that glycolysis was inhibited. Glycogen 63-71 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 12689664-2 2003 77IL-8 was significantly converted to 72IL-8 by a partially purified fraction of the culture supernatant of human diploid fibroblasts. 72il-8 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 2-6 12701778-0 2003 Effect of an intraosseous injection of depo-medrol on pulpal concentrations of PGE2 and IL-8 in untreated irreversible pulpitis. Methylprednisolone Acetate 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12679464-9 2003 Treatment of fetal membranes with NAC significantly suppressed lipopolysaccharide-stimulated type II phospholipase A(2) release and content; PGF(2alpha), IL-6, IL-8, TNFalpha, and 8-isoprostane release; and matrix metalloproteinase-9 and urokinase-type plasminogen activator enzyme activity and suppressed NF-kappaB DNA-binding activity (by ANOVA, P < 0.05). Acetylcysteine 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 14679759-0 2003 [Suppressive mechanism of clarithromycin on lipopolysaccharide-induced IL-8 production in human monocytes by mediating AP-1 and NF-kappaB]. Clarithromycin 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 12639123-1 2003 The dissolution and complex formation of fluoroaluminates in two eutectic alkalifluoride mixtures, NaF-KF (FNAK) and LiF-NaF-KF (FLINAK), have been investigated by Raman, NMR, and thermal analysis. fluoroaluminum 41-57 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 12841342-0 2003 The effect of early treatment by cerivastatin on the serum level of C-reactive protein, interleukin-6, and interleukin-8 in the patients with unstable angina and non-Q-wave myocardial infarction. cerivastatin 33-45 C-X-C motif chemokine ligand 8 Homo sapiens 107-120 12841342-1 2003 The aim of our study was to evaluate whether a single dose of cerivastatin at the time of admission of patients with unstable angina pectoris (UAP) or non-Q-wave myocardial infarction (NQMI) can influence the serum level of C-reactive protein (CRP), interleukin-6 (IL-6) and interleukin-8 (IL-8) 24 h later. cerivastatin 62-74 C-X-C motif chemokine ligand 8 Homo sapiens 275-288 12841342-1 2003 The aim of our study was to evaluate whether a single dose of cerivastatin at the time of admission of patients with unstable angina pectoris (UAP) or non-Q-wave myocardial infarction (NQMI) can influence the serum level of C-reactive protein (CRP), interleukin-6 (IL-6) and interleukin-8 (IL-8) 24 h later. cerivastatin 62-74 C-X-C motif chemokine ligand 8 Homo sapiens 290-294 12628462-4 2003 IL-8 release was measured by ELISA from cells activated for 6 h with TNFalpha (50 ng ml(-1)) in the absence and presence of nicotine (10(-11)-10(-6) M). Nicotine 124-132 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12628462-7 2003 Nicotine significantly inhibited TNFalpha-induced IL-8 release in a concentration related manner with peak inhibition occurring at 10(-7) M (2.39 +/- 0.78 ng ml(-1), n = 5). Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12600879-4 2003 The adenosine agonist NECA (100 micromol/L) increased interleukin-8 (IL-8), vascular endothelial growth factor (VEGF), and angiopoietin-2 mRNA expression. Adenosine-5'-(N-ethylcarboxamide) 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 12600879-4 2003 The adenosine agonist NECA (100 micromol/L) increased interleukin-8 (IL-8), vascular endothelial growth factor (VEGF), and angiopoietin-2 mRNA expression. Adenosine-5'-(N-ethylcarboxamide) 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 12600879-4 2003 The adenosine agonist NECA (100 micromol/L) increased interleukin-8 (IL-8), vascular endothelial growth factor (VEGF), and angiopoietin-2 mRNA expression. Adenosine 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 12600879-4 2003 The adenosine agonist NECA (100 micromol/L) increased interleukin-8 (IL-8), vascular endothelial growth factor (VEGF), and angiopoietin-2 mRNA expression. Adenosine 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 12600879-6 2003 A2B receptors mediate VEGF and IL-8 secretion because neither CGS21680 (selective A2A agonist) nor IB-MECA (selective A3 agonist) produced this effect, and it was inhibited by the selective A2B antagonist IPDX but not by the selective A2A antagonist SCH58261 or the selective A3 antagonist MRS1191. 3-isobutyl-8-pyrrolidinoxanthine 205-209 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 12600878-0 2003 Glucose regulates monocyte adhesion through endothelial production of interleukin-8. Glucose 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 12646250-0 2003 Ergothioneine inhibits oxidative stress- and TNF-alpha-induced NF-kappa B activation and interleukin-8 release in alveolar epithelial cells. Ergothioneine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 12646250-4 2003 The aim of this study was to determine whether ergothioneine can inhibit the hydrogen peroxide (H(2)O(2))- and TNF-alpha-mediated activation of NF-kappa B and the release of IL-8 in human alveolar epithelial cells (A549). Ergothioneine 47-60 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 12646250-4 2003 The aim of this study was to determine whether ergothioneine can inhibit the hydrogen peroxide (H(2)O(2))- and TNF-alpha-mediated activation of NF-kappa B and the release of IL-8 in human alveolar epithelial cells (A549). Hydrogen Peroxide 77-94 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 12646250-4 2003 The aim of this study was to determine whether ergothioneine can inhibit the hydrogen peroxide (H(2)O(2))- and TNF-alpha-mediated activation of NF-kappa B and the release of IL-8 in human alveolar epithelial cells (A549). Hydrogen Peroxide 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 12646250-7 2003 Both H(2)O(2) and TNF-alpha significantly increased IL-8 release, which was inhibited by pre-treatment of A549 cells with ergothioneine compared to the control untreated cells. Hydrogen Peroxide 5-13 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 12646250-7 2003 Both H(2)O(2) and TNF-alpha significantly increased IL-8 release, which was inhibited by pre-treatment of A549 cells with ergothioneine compared to the control untreated cells. Ergothioneine 122-135 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 12646250-8 2003 Ergothioneine also abolished the transcriptional activation of IL-8 in an IL-8-chloramphenicol acetyltransferase (CAT) reporter system, transfected into A549 cells. Ergothioneine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 12646250-8 2003 Ergothioneine also abolished the transcriptional activation of IL-8 in an IL-8-chloramphenicol acetyltransferase (CAT) reporter system, transfected into A549 cells. Ergothioneine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 12600878-6 2003 Analysis of the human IL-8 promoter revealed binding sites for NF-kappaB and AP-1 as well as several aligned carbohydrate response elements (also known as E-boxes). Carbohydrates 109-121 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 12600878-7 2003 Glucose dramatically stimulated IL-8 promoter activity. Glucose 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 12600878-8 2003 Using mutated IL-8 promoter constructs and EMSA, we found that the AP-1 element and the glucose-response element were responsible for much of the glucose-mediated activation of IL-8 transcription. Glucose 88-95 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 12627953-9 2003 In contrast, in CXCR2-RBL cells the migration-attenuating concentrations of IL-8 induced promoted levels of FAK phosphorylation and different patterns of FAK phosphorylation on its six potential tyrosine phosphorylation sites, as compared to activating concentrations of the chemokine. Tyrosine 195-203 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 12600878-2 2003 HAECs cultured for 7 days in 25 mmol/L glucose had a 2-fold elevation in interleukin-8 (IL-8) secretion over control cells cultured in 5.5 mmol/L glucose (P<0.001). Glucose 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 12600878-8 2003 Using mutated IL-8 promoter constructs and EMSA, we found that the AP-1 element and the glucose-response element were responsible for much of the glucose-mediated activation of IL-8 transcription. Glucose 146-153 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 12600878-8 2003 Using mutated IL-8 promoter constructs and EMSA, we found that the AP-1 element and the glucose-response element were responsible for much of the glucose-mediated activation of IL-8 transcription. Glucose 146-153 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 12600878-2 2003 HAECs cultured for 7 days in 25 mmol/L glucose had a 2-fold elevation in interleukin-8 (IL-8) secretion over control cells cultured in 5.5 mmol/L glucose (P<0.001). Glucose 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12600878-9 2003 Interestingly, inhibition of reactive oxygen species (ROS) production through use of pharmacological uncouplers of the mitochondrial electron transport chain significantly reduced glucose-mediated induction of IL-8 expression. Reactive Oxygen Species 29-52 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 12600878-3 2003 Use of a neutralizing antibody to IL-8 prevented glucose-mediated monocyte adhesion. Glucose 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 12600878-9 2003 Interestingly, inhibition of reactive oxygen species (ROS) production through use of pharmacological uncouplers of the mitochondrial electron transport chain significantly reduced glucose-mediated induction of IL-8 expression. Reactive Oxygen Species 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 12600878-9 2003 Interestingly, inhibition of reactive oxygen species (ROS) production through use of pharmacological uncouplers of the mitochondrial electron transport chain significantly reduced glucose-mediated induction of IL-8 expression. Glucose 180-187 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 12695126-1 2003 The CXC-chemokines Groalpha and interleukin-8 (IL-8) are ligands for two different G protein-coupled receptors, named CXC-chemokine receptor I & II (CXCRI & II). Adenosine Monophosphate 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 12600878-10 2003 These data indicate that glucose regulates monocyte:endothelial interactions through stimulation of IL-8 and ROS production and activation of the alpha5beta1 integrin complex on HAECs. Glucose 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 12573991-5 2003 PM(10) and H(2)O(2) increased IL-8 protein release from A549 cells after 24-h treatment, and this was enhanced by histone deacetylase inhibition by trichostatin A (cotreatment). trichostatin A 148-162 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 12653753-8 2003 Relative levels of transcripts for IL-8, MIP-1alpha, TNF-alpha and IL-2 were lower at the end of each individual DFPP and after the four treatments than at the beginning of treatment. dfpp 113-117 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 12650786-12 2003 Again, the IL-8 levels were significantly decreased after lansoprazole treatment. Lansoprazole 58-70 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 12695126-1 2003 The CXC-chemokines Groalpha and interleukin-8 (IL-8) are ligands for two different G protein-coupled receptors, named CXC-chemokine receptor I & II (CXCRI & II). Adenosine Monophosphate 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12695126-1 2003 The CXC-chemokines Groalpha and interleukin-8 (IL-8) are ligands for two different G protein-coupled receptors, named CXC-chemokine receptor I & II (CXCRI & II). Adenosine Monophosphate 160-163 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 12695126-1 2003 The CXC-chemokines Groalpha and interleukin-8 (IL-8) are ligands for two different G protein-coupled receptors, named CXC-chemokine receptor I & II (CXCRI & II). Adenosine Monophosphate 160-163 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12629150-5 2003 The Fas agonistic antibody CH-11 dose-dependently stimulated the expression of IL-6 and IL-8 in glioma cells. 4-dimethylamino-3',4'-dimethoxychalcone 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12703484-5 2003 The predicted IL-8 peptide had one potential N-linked glycosylation site (Asn-72-Thr-74) that is not conserved in other vertebrates. Nitrogen 45-46 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 12555204-6 2003 We found that QUIN induces astrocytes to produce large quantities of MCP-1 (CCL2) and lesser amounts of RANTES (CCL5) and IL-8 (CXCL8). Quinolinic Acid 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 12555204-6 2003 We found that QUIN induces astrocytes to produce large quantities of MCP-1 (CCL2) and lesser amounts of RANTES (CCL5) and IL-8 (CXCL8). Quinolinic Acid 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 128-133 12580917-6 2003 RESULTS: Using H292 cells, EGF and H2O2 increased IL-8 gene expression and release and this was completely suppressed by the EGFR-selective tyrosine kinase inhibitor, AG1478, but only partially by dexamethasone. Hydrogen Peroxide 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12393592-1 2003 Some cases of heparin-induced thrombocytopenia (HIT) have been reported to be associated with antibodies against interleukin-8 (IL-8), a chemokine related to platelet factor 4. Heparin 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 12393592-1 2003 Some cases of heparin-induced thrombocytopenia (HIT) have been reported to be associated with antibodies against interleukin-8 (IL-8), a chemokine related to platelet factor 4. Heparin 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 12576442-8 2003 All six anti-inflammatory agents suppressed induction of IL-8 mRNA expression in lung cancer cells by >90%, four (pentoxifylline, celecoxib, pyrrolidine dithiocarbamate, and dexamethasone) having a dose-dependent effect. Pentoxifylline 117-131 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 12576442-8 2003 All six anti-inflammatory agents suppressed induction of IL-8 mRNA expression in lung cancer cells by >90%, four (pentoxifylline, celecoxib, pyrrolidine dithiocarbamate, and dexamethasone) having a dose-dependent effect. Celecoxib 133-142 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 12576442-8 2003 All six anti-inflammatory agents suppressed induction of IL-8 mRNA expression in lung cancer cells by >90%, four (pentoxifylline, celecoxib, pyrrolidine dithiocarbamate, and dexamethasone) having a dose-dependent effect. pyrrolidine dithiocarbamic acid 144-171 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 12393592-3 2003 This activation occurred at IL-8 concentrations achievable in vivo and was facilitated by heparin (0.1 U/mL). Heparin 90-97 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 12580917-6 2003 RESULTS: Using H292 cells, EGF and H2O2 increased IL-8 gene expression and release and this was completely suppressed by the EGFR-selective tyrosine kinase inhibitor, AG1478, but only partially by dexamethasone. RTKI cpd 167-173 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12576442-8 2003 All six anti-inflammatory agents suppressed induction of IL-8 mRNA expression in lung cancer cells by >90%, four (pentoxifylline, celecoxib, pyrrolidine dithiocarbamate, and dexamethasone) having a dose-dependent effect. Dexamethasone 177-190 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 12629330-0 2003 Dual response to Fas ligation in human endothelial cells: apoptosis and induction of chemokines, interleukin-8 and monocyte chemoattractant protein-1. ammonium ferrous sulfate 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 12629330-4 2003 We also investigated whether an inhibitor of caspase-8 (Z-IETD-FMK) does modulate IL-8 and MCP-1 secretion. benzyloxycarbonyl-isoleucyl-glutamyl-threonyl-aspartic acid fluoromethyl ketone 56-66 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 12576957-9 2003 Patients fed EPA+GLA had a significant reduction in BALF ceruloplasmin and IL-8 during the study as compared with patients fed the control diet. epa+gla 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 12629330-9 2003 Fas-neutralizing agent (Fas-Fc) suppressed the Fas-mediated secretions of IL-8 and MCP-1 (P < 0.01) both as well as the Fas-mediated apoptosis. ammonium ferrous sulfate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 12629330-9 2003 Fas-neutralizing agent (Fas-Fc) suppressed the Fas-mediated secretions of IL-8 and MCP-1 (P < 0.01) both as well as the Fas-mediated apoptosis. ammonium ferrous sulfate 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 12629330-9 2003 Fas-neutralizing agent (Fas-Fc) suppressed the Fas-mediated secretions of IL-8 and MCP-1 (P < 0.01) both as well as the Fas-mediated apoptosis. ammonium ferrous sulfate 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 12629330-9 2003 Fas-neutralizing agent (Fas-Fc) suppressed the Fas-mediated secretions of IL-8 and MCP-1 (P < 0.01) both as well as the Fas-mediated apoptosis. ammonium ferrous sulfate 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 12629330-10 2003 On the other hand, whereas Z-IETD-FMK suppressed apoptosis, the inhibitor enhanced the Fas-mediated secretions of both IL-8 and MCP-1 beyond the value of the Fas stimulation alone (P < 0.01), suggesting an enhanced signalling for the chemokine expression. benzyloxycarbonyl-isoleucyl-glutamyl-threonyl-aspartic acid fluoromethyl ketone 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12629330-10 2003 On the other hand, whereas Z-IETD-FMK suppressed apoptosis, the inhibitor enhanced the Fas-mediated secretions of both IL-8 and MCP-1 beyond the value of the Fas stimulation alone (P < 0.01), suggesting an enhanced signalling for the chemokine expression. ammonium ferrous sulfate 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12588289-8 2003 Additionally, serum IL-1beta, IL-6 and, especially, IL-8 levels were significantly higher in the subjects with than in those without ABG (P < 0.0001, for all cytokines). abg 133-136 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 12588289-12 2003 CONCLUSIONS: The ratio between serum IL-8 and pepsinogen A/C accurately predicts the presence of ABG. abg 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 12586608-4 2003 CS and CT strongly inhibited the production of proinflammatory cytokines (IL-1alpha, IL-1beta, IL-6, IL-8, and TNF-alpha) from LPS-stimulated human monocytes. Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 12586608-4 2003 CS and CT strongly inhibited the production of proinflammatory cytokines (IL-1alpha, IL-1beta, IL-6, IL-8, and TNF-alpha) from LPS-stimulated human monocytes. ct 7-9 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 12588890-12 2003 In conclusion, albumin is a strong stimulus for tubular IL-8 expression, which occurs via NF-kappaB-dependent pathways through PKC activation and ROS generation. Reactive Oxygen Species 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 12574206-5 2003 The NF-kappa B inhibitor, N-tosyl-L-phenylalanine chloromethyl ketone, reduced TNFalpha-induced IL-8 gene and protein expression. Tosylphenylalanyl Chloromethyl Ketone 26-69 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 12574206-9 2003 The addition of estradiol (E2; 10(-7) M) enhanced the expression of IL-8. Estradiol 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 12588890-7 2003 NF-kappaB activation and IL-8 secretion were attenuated by the NF-kappaB inhibitors pyrrolidine dithiocarbamate and cell-permeable peptide. pyrrolidine dithiocarbamic acid 84-111 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 12588890-8 2003 Albumin upregulated intracellular reactive oxygen species (ROS) generation, while exogenous H2O2 stimulated NF-kappaB translocation and IL-8 secretion. Hydrogen Peroxide 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 12588890-9 2003 Albumin-induced ROS generation, NF-kappaB activation, and IL-8 secretion were endocytosis- and PKC-dependent as these downstream events were abrogated by the PI3K inhibitors LY294002 and wortmannin, and the PKC inhibitors GF109203X and staurosporin, respectively. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 174-182 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12588890-9 2003 Albumin-induced ROS generation, NF-kappaB activation, and IL-8 secretion were endocytosis- and PKC-dependent as these downstream events were abrogated by the PI3K inhibitors LY294002 and wortmannin, and the PKC inhibitors GF109203X and staurosporin, respectively. Wortmannin 187-197 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12504339-9 2003 Overall, PB infusion caused a decrease or IL-8 and PGE(2) release. Pyridostigmine Bromide 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 12646971-5 2003 Plasma and bronchoalveolar lavage fluid (BALF) IL-8 levels in the control group were significantly higher than those in the steroid group. Steroids 124-131 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12594001-11 2003 IL-8 produced by CSMCs in response to gram-negative infection may promote neutrophil invasion, and release of neutrophil matrix-degrading enzymes may participate in the matrix remodeling associated with parturition. csmcs 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12745544-9 2003 Clearance of IL-8 increased by 0.47+/-0.08 pg/ml for each unit increase in pre-dialysis IL-8 (p<0.001) and decreased by 5.63+/-2.59 pg/ml for each unit increase in pre-dialysis urea mmol/l (p<0.05). Urea 180-184 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 12504339-12 2003 IL-8 was assayed at 1, 2, 4, 8, 12 and 24 h. PB suppressed IL-8 in permethrin and ethanol treatment from 4 to 24 h confirming the IPPSF results. Permethrin 67-77 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 12554889-10 2003 Moreover, there was a significant negative correlation between peroxynitrite inhibitory activity and the degree of neutrophilic inflammation (percentage of neutrophils: r=-0.754, p<0.001; IL-8 levels: r=-0.497, p=0.007). Peroxynitrous Acid 63-76 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 12504339-13 2003 In conclusion, these studies suggest that systemic exposure to PB suppressed IL-8 release at multiple time points in two skin model systems. Pyridostigmine Bromide 63-65 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 12406856-2 2003 We investigated the effect of dexamethasone on basal and interleukin (IL)-1beta or cigarette smoke media (CSM)-stimulated release of IL-8 and granulocyte macrophage-colony stimulating factor (GM-CSF) by bronchoalveolar lavage macrophages from cigarette smokers and patients with COPD (n = 15). Dexamethasone 30-43 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 12471616-7 2003 In contrast, highly tumorigenic and metastatic 451Lu cells showed marked increases in tumor growth and number of metastatic foci in the lungs depending on the expression levels of IL-8. 451lu 47-52 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 12505195-0 2003 Pyrrolidinedithiocarbamate inhibits NF-kappaB activation and IL-8 production in intestinal epithelial cells. pyrrolidine dithiocarbamic acid 0-26 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 12505195-4 2003 In the present paper we investigated the effect of pharmacological inhibition of NF-kappaB with pyrrolidinedithiocarbamate (PDTC) on IL-1beta-induced IL-8 production by the human intestinal epithelial cell line HT-29. pyrrolidine dithiocarbamic acid 96-122 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 12505195-4 2003 In the present paper we investigated the effect of pharmacological inhibition of NF-kappaB with pyrrolidinedithiocarbamate (PDTC) on IL-1beta-induced IL-8 production by the human intestinal epithelial cell line HT-29. pyrrolidine dithiocarbamic acid 124-128 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 12471621-0 2003 Induction of IL-8 and monoclyte chemoattractant protein-1 by doxorubicin in human small cell lung carcinoma cells. Doxorubicin 61-72 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 12471621-3 2003 We have, therefore, extended the observation by testing the effects of doxorubicin on expression of the chemokine family and provide here definitive evidence that doxorubicin induces IL-8 and MCP-1, one of the CC chemokines, at least in 2 human SCLC cells, H69 and SBC-1. Doxorubicin 163-174 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 12471621-4 2003 IL-8 antigen levels, measured by ELISA, were markedly increased in both H69 and SBC-1 conditioned media after doxorubicin treatment, in parallel with mRNA levels; and this was dependent on the dose of doxorubicin. Doxorubicin 110-121 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12471621-4 2003 IL-8 antigen levels, measured by ELISA, were markedly increased in both H69 and SBC-1 conditioned media after doxorubicin treatment, in parallel with mRNA levels; and this was dependent on the dose of doxorubicin. Doxorubicin 201-212 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12471621-5 2003 The ribonuclease protection assay, using a multiprobe template set for human chemokines, revealed induction of not only IL-8 but also MCP-1 in doxorubicin-treated H69 cells. Doxorubicin 143-154 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 12471621-10 2003 IL-8 and MCP-1 are major chemoattractants for neutrophils and monocytes/macrophages, respectively; therefore, extensive induction of IL-8 and MCP-1 may provoke the interaction between inflammatory/immune cells and tumor cells under doxorubicin stimulation and influence many aspects of tumor cell biology. Doxorubicin 232-243 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12471621-10 2003 IL-8 and MCP-1 are major chemoattractants for neutrophils and monocytes/macrophages, respectively; therefore, extensive induction of IL-8 and MCP-1 may provoke the interaction between inflammatory/immune cells and tumor cells under doxorubicin stimulation and influence many aspects of tumor cell biology. Doxorubicin 232-243 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 15206714-6 2003 We found that QUIN induces astrocytes to produce large quantities of MCP-1 (CCL2), and lesser amounts of RANTES (CCL5), IL-8 (CXCL8). Quinolinic Acid 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 15206714-6 2003 We found that QUIN induces astrocytes to produce large quantities of MCP-1 (CCL2), and lesser amounts of RANTES (CCL5), IL-8 (CXCL8). Quinolinic Acid 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 126-131 12507912-2 2003 The present study was undertaken to evaluate the effects of anti-inflammatory cytokine interleukin-10 (IL-10) on NaCl-induced chemokine IL-8 and regulated on activation normal T cell expressed and secreted (RANTES) expression through the NF-kappaB signaling in primary deltaF508 CF and non-CF (control) human bronchial epithelial cells. Sodium Chloride 113-117 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 12507912-4 2003 Compared to non-CF cells, CF bronchial epithelial cells were characterized by a higher susceptibility to produce elevated IL-8 and RANTES production in an hypertonic NaCl milieu in response to IL-1beta activation. Sodium Chloride 166-170 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 12393716-7 2003 By contrast, the induction of interleukin-8 was delayed and was found to be cyclosporine insensitive. Cyclosporine 76-88 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 14646051-1 2003 Introducing the theory of fuzzy set, mathematical morphology and computerized mask fast scanning, we developed the TOOTH.SCA software and method to analyze the effect of fluoride (NaF) on ore content of human tooth enamel automatically and quantitatively. Fluorides 170-178 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 12419628-6 2003 When the NaF concentration was higher than 0.1%, the protectiveness of TiO(2) passive film formed on Ti-6Al-4V alloy was destroyed by fluoride ions, leading to the formation of Na(2)TiF(6). tio 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 12419628-6 2003 When the NaF concentration was higher than 0.1%, the protectiveness of TiO(2) passive film formed on Ti-6Al-4V alloy was destroyed by fluoride ions, leading to the formation of Na(2)TiF(6). Fluorides 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 12419628-6 2003 When the NaF concentration was higher than 0.1%, the protectiveness of TiO(2) passive film formed on Ti-6Al-4V alloy was destroyed by fluoride ions, leading to the formation of Na(2)TiF(6). na(2)tif 177-185 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 12600410-0 2003 Modulation of interleukin-8 and nitric oxide synthase mRNA levels by interferon-gamma in macrophages stimulated with lignin derivatives and lipopolysaccharides. Lignin 117-123 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 12519386-3 2003 IL-8 promoter activity in IEC pretreated with butyrate then exposed to proinflammatory stimuli was assayed by transfection of luciferase constructs. Butyrates 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 14642531-4 2003 This polarity did not correlate with glycosylation, as IL-8 and MIC-1 are both N-glycosylated, but were sorted to opposite sides of the cell. Nitrogen 79-80 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 12788054-7 2003 Hydrocortisone at a dose, which inhibits cell death also down regulated, the expression of pro-inflammatory cytokines IL-6 and IL-8. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 12519386-9 2003 Pharmacological inhibition of protein tyrosine phosphatases or treatment with mesalamine or sulphasalazine diminished IL-1 beta-stimulated IL-8 secretion by butyrate-exposed HT-29 cells substantially. Sulfasalazine 92-106 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 12519386-6 2003 Butyrate modulated proinflammatory IL-8 secretion differentially in Caco-2 and HT-29 cells on the transcriptional level. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 12519386-9 2003 Pharmacological inhibition of protein tyrosine phosphatases or treatment with mesalamine or sulphasalazine diminished IL-1 beta-stimulated IL-8 secretion by butyrate-exposed HT-29 cells substantially. Butyrates 157-165 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 12538487-8 2003 Inhibiting NFkappaB activation by expressing IkappaBalphaM and using pharmacologic NFkappaB inhibitor PS-341 also significantly reduced cytokine-induced vascular endothelial growth factor and interleukin-8 expression in AsPc-1 pancreatic cancer cells. Bortezomib 102-108 C-X-C motif chemokine ligand 8 Homo sapiens 192-205 12519386-11 2003 Pharmacological inhibition of enhanced IL-1 beta-mediated IL-8 secretion in a subpopulation of IEC may improve the clinical efficacy of butyrate. Butyrates 136-144 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12519386-7 2003 Pointing to the potentially underlying mechanism of increased IL-1 beta-stimulated IL-8 secretion in HT-29 cells, butyrate up-regulated IL-1RI mRNA but not IL-1RII. Butyrates 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 12519386-9 2003 Pharmacological inhibition of protein tyrosine phosphatases or treatment with mesalamine or sulphasalazine diminished IL-1 beta-stimulated IL-8 secretion by butyrate-exposed HT-29 cells substantially. Mesalamine 78-88 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 12498928-7 2003 We conclude that in HT-29 cells, TNF-alpha-induced interleukin-8 release is inhibited by cannabinoids through activation of cannabinoid CB(2) receptors. Cannabinoids 89-101 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 12498928-0 2003 Inhibition of interleukin-8 release in the human colonic epithelial cell line HT-29 by cannabinoids. Cannabinoids 87-99 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 12499080-2 2003 MEM significantly inhibited PMA-induced secretions of IL-8 and MCP-1 proteins in a dose-dependent manner. Tetradecanoylphorbol Acetate 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 12498928-1 2003 We have investigated the effects of cannabinoid agonists and antagonists on tumour necrosis factor-alpha (TNF-alpha)-induced secretion of interleukin-8 from the colonic epithelial cell line, HT-29. Cannabinoids 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 138-151 12458377-13 2003 Butyrate down-regulated TLR 4 expression and significantly diminished LPS-dependent IL-8 secretion. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 14595851-4 2003 Furthermore, macroarray analysis showed that naphthalene modified cord blood gene expression, inducing IL-8 precursor and T-cell transcription factor and decreasing the level of RNA-binding protein FUS/TLS. naphthalene 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 12499080-4 2003 In addition, 1,2,3,4,6-penta-O-galloyl-beta-D-glucose, one of major constituents isolated from MEM, inhibited PMA-induced secretions of IL-8 and MCP-1 proteins by its suppression of IL-8 and MCP-1 genes. beta-penta-O-galloyl-glucose 13-53 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 12499080-4 2003 In addition, 1,2,3,4,6-penta-O-galloyl-beta-D-glucose, one of major constituents isolated from MEM, inhibited PMA-induced secretions of IL-8 and MCP-1 proteins by its suppression of IL-8 and MCP-1 genes. beta-penta-O-galloyl-glucose 13-53 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 12499080-4 2003 In addition, 1,2,3,4,6-penta-O-galloyl-beta-D-glucose, one of major constituents isolated from MEM, inhibited PMA-induced secretions of IL-8 and MCP-1 proteins by its suppression of IL-8 and MCP-1 genes. Tetradecanoylphorbol Acetate 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 12499080-4 2003 In addition, 1,2,3,4,6-penta-O-galloyl-beta-D-glucose, one of major constituents isolated from MEM, inhibited PMA-induced secretions of IL-8 and MCP-1 proteins by its suppression of IL-8 and MCP-1 genes. Tetradecanoylphorbol Acetate 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 12556010-0 2003 Effects by 8-bromo-cyclicAMP on basal and organic dust-induced release of interleukin-6 and interleukin-8 in A549 human airway epithelial cells. 8-Bromo Cyclic Adenosine Monophosphate 11-28 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 12544908-6 2003 RESULTS: Increases in IL-8, IL-6, and IL-10 were greater in patients resuscitated with PRBCs. prbcs 87-92 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 12934311-4 2003 Carvedilol group of patients demonstrated a marked trend to reduction of the number of hospitalizations, attenuation of CCF, better tolerance to exercise, lower levels of uric acid (p < 0.05), malonic dialdehyde (p < 0.05) and IL-8 (p = 0.09). Carvedilol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 12490594-9 2003 Activation of the epidermal VR1 by capsaicin also resulted in an increased release of interleukin-8 and prostaglandin E2, and the stimulated release was attenuated by capsazepine. Capsaicin 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 12490594-9 2003 Activation of the epidermal VR1 by capsaicin also resulted in an increased release of interleukin-8 and prostaglandin E2, and the stimulated release was attenuated by capsazepine. capsazepine 167-178 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 14605444-0 2003 Depolymerization of actin filament by cytochalasin E induces interleukin-8 production and up-regulates CD54 in the HeLa epithelial cell line. cytochalasin E 38-52 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 14605444-4 2003 In this study, we found that cytochalasin E strongly induces interleukin-8 through an epithelial cell line, HeLa, in dose- and time-dependent manners as assessed by enzyme-linked immunoassay and reverse transcription-polymerase chain reaction techniques. cytochalasin E 29-43 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 14605444-5 2003 In addition, interleukin-8 production in the HeLa cells cultured with cytochalasin E was blocked in the presence of protein kinase C inhibitors, Go6976 and H-7. cytochalasin E 70-84 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 14605444-5 2003 In addition, interleukin-8 production in the HeLa cells cultured with cytochalasin E was blocked in the presence of protein kinase C inhibitors, Go6976 and H-7. Go 6976 145-151 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 14605444-7 2003 Taken together, these findings indicate that cytochalasin E activates protein kinase C under the depolymerization of actin filament, leading to the induction of interleukin-8 production and the up-regulation of CD54 in HeLa cells. cytochalasin E 45-59 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 12556010-4 2003 We therefore investigated whether 8-Bromo-cAMP, a cell membrane-permeable cAMP analogue, would influence release of the cytokines interleukin-6 (IL-6) and IL-8 in a human airway epithelial cell line, A549, exposed to a suspension of the organic dust, and to a supernatant prepared by centrifugation (at low g-force) of a suspension of dust. 8-Bromo Cyclic Adenosine Monophosphate 34-46 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 12556010-4 2003 We therefore investigated whether 8-Bromo-cAMP, a cell membrane-permeable cAMP analogue, would influence release of the cytokines interleukin-6 (IL-6) and IL-8 in a human airway epithelial cell line, A549, exposed to a suspension of the organic dust, and to a supernatant prepared by centrifugation (at low g-force) of a suspension of dust. Cyclic AMP 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 12556010-9 2003 8-Bromo-cAMP did not affect basal IL-8 release, partially inhibited (28%) the release of IL-8 induced by a dust suspension (P<0.01), but increased IL-8 release induced by a dust supernatant by 13% (P<0.05). 8-Bromo Cyclic Adenosine Monophosphate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 12556010-9 2003 8-Bromo-cAMP did not affect basal IL-8 release, partially inhibited (28%) the release of IL-8 induced by a dust suspension (P<0.01), but increased IL-8 release induced by a dust supernatant by 13% (P<0.05). 8-Bromo Cyclic Adenosine Monophosphate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 12556010-10 2003 In summary, expression of the cytokines IL-6 and IL-8 is differentially regulated by 8-Bromo-cAMP, both with regard to basal and dust-induced release. 8-Bromo Cyclic Adenosine Monophosphate 85-97 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 12556010-11 2003 The results indicate that 8-Bromo-cAMP attenuated IL-8 release by affecting signaling transductions induced by the particulate fraction. 8-Bromo Cyclic Adenosine Monophosphate 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12492348-1 2002 The [1 + 2] cycloaddition reaction of 1-iodoalkynes with difluorocarbene, generated from the decomposition of FSO(2)CF(2)COOSiMe(3) in diglyme in the presence of 10 mol % NaF at 120 degrees C, gives 3,3-difluoro-1-iodocyclopropenes in good yields. 1-iodoalkynes 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 12729367-4 2003 It has been hypothesized that the link between cisplatin treatment and FMF attacks lies in an increased production of serotonin, IL-6, IL-1, IL-8 and TNF-alpha. Cisplatin 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 12492348-1 2002 The [1 + 2] cycloaddition reaction of 1-iodoalkynes with difluorocarbene, generated from the decomposition of FSO(2)CF(2)COOSiMe(3) in diglyme in the presence of 10 mol % NaF at 120 degrees C, gives 3,3-difluoro-1-iodocyclopropenes in good yields. difluorocarbene 57-72 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 12492348-1 2002 The [1 + 2] cycloaddition reaction of 1-iodoalkynes with difluorocarbene, generated from the decomposition of FSO(2)CF(2)COOSiMe(3) in diglyme in the presence of 10 mol % NaF at 120 degrees C, gives 3,3-difluoro-1-iodocyclopropenes in good yields. diglyme 135-142 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 12471139-6 2002 Depletion of tryptophan led to stabilization of IL-6 and IL-8 mRNA and increased IL-6 and IL-8 responses, whereas supplementing tryptophan largely restored these changes. Tryptophan 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 12471139-6 2002 Depletion of tryptophan led to stabilization of IL-6 and IL-8 mRNA and increased IL-6 and IL-8 responses, whereas supplementing tryptophan largely restored these changes. Tryptophan 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 12413740-7 2002 Increased IL-8 secretion due to endomorphin-1 could be blocked by pre-incubating cells with the mu receptor antagonist, beta-funaltrexamine. beta-funaltrexamine 120-139 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 12432545-0 2002 The copper chelator trientine has an antiangiogenic effect against hepatocellular carcinoma, possibly through inhibition of interleukin-8 production. Copper 4-10 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 12432545-0 2002 The copper chelator trientine has an antiangiogenic effect against hepatocellular carcinoma, possibly through inhibition of interleukin-8 production. Trientine 20-29 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 12432545-10 2002 The production of IL-8 from the tumor was suppressed by trientine. Trientine 56-65 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 12432545-11 2002 In vitro, IL-8 production by HuH-7 cells in copper-containing medium was significantly greater than that in copper-free medium, and this effect was weakened when trientine was added. Copper 44-50 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 12432545-11 2002 In vitro, IL-8 production by HuH-7 cells in copper-containing medium was significantly greater than that in copper-free medium, and this effect was weakened when trientine was added. Copper 108-114 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 12432545-11 2002 In vitro, IL-8 production by HuH-7 cells in copper-containing medium was significantly greater than that in copper-free medium, and this effect was weakened when trientine was added. Trientine 162-171 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 12432545-13 2002 In conclusion, the chelating effect of trientine prevented copper from functioning as a cofactor in angiogenesis, which resulted in reduced IL-8 production from HuH-7 cells. Trientine 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 12432545-13 2002 In conclusion, the chelating effect of trientine prevented copper from functioning as a cofactor in angiogenesis, which resulted in reduced IL-8 production from HuH-7 cells. Copper 59-65 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 12452835-6 2002 In the A549 cells, gp-340 was up-regulated along with the PMA-induced proinflammatory expression of both IL-6 and IL-8. Tetradecanoylphorbol Acetate 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 12558191-8 2002 IL-8 "hyper-responders" experienced significantly greater postoperative weight gain and had higher IL-8 levels at 24 h (p<0.05), with trends towards renal impairment and protracted supplemental oxygen requirements. Oxygen 197-203 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12442335-6 2002 The presence of wortmannin during receptor recycling inhibited CXCR1 and CXCR2 re-expression following CXCL8-induced internalization, and resulted in a marked disruption of the proper organization of actin filaments. Wortmannin 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 103-108 12438368-3 2002 As CAP37 and protamines share high levels of arginine content, we tested different synthetic poly-L-amino acids and found that poly-L-arginine, and to a lesser extent poly-L-lysine, increased IL-8 production in LPS-stimulated human whole blood. polyarginine 127-142 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 12438368-3 2002 As CAP37 and protamines share high levels of arginine content, we tested different synthetic poly-L-amino acids and found that poly-L-arginine, and to a lesser extent poly-L-lysine, increased IL-8 production in LPS-stimulated human whole blood. Lysine 167-180 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 12473064-3 2002 Lipopolysaccharide stimulated IL-8 production in 8-MOP-phototreated PBMC more efficiently than those untreated or treated with 8-MOP or UVA. Methoxsalen 49-54 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 12488495-7 2002 These findings suggest that ethanol may modulate three major cytokines involved in alcoholic liver diseases, IL-8, TNF-alpha, and HGF, via three different mechanisms. Ethanol 28-35 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 12444152-3 2002 In the present study, we demonstrate that a potent and selective nonpeptide antagonist of human CXCR2 potently inhibits (125)I-labeled human IL-8 binding to, and human IL-8-induced calcium mobilization mediated by, rabbit CXCR2 (IC(50) = 40.5 and 7.7 nM, respectively), but not rabbit CXCR1 (IC(50) = >1000 and 2200 nM, respectively). Calcium 181-188 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 12444152-3 2002 In the present study, we demonstrate that a potent and selective nonpeptide antagonist of human CXCR2 potently inhibits (125)I-labeled human IL-8 binding to, and human IL-8-induced calcium mobilization mediated by, rabbit CXCR2 (IC(50) = 40.5 and 7.7 nM, respectively), but not rabbit CXCR1 (IC(50) = >1000 and 2200 nM, respectively). Calcium 181-188 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 12379337-2 2002 Two main forms of IL-8 exist, one containing 77 amino acids (Ala-IL-8(77)) and a second containing 72 amino acids (Ser-IL-8(72)), which comprise more than 90% of IL-8 protein in cell cultures. Alanine 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 12379337-2 2002 Two main forms of IL-8 exist, one containing 77 amino acids (Ala-IL-8(77)) and a second containing 72 amino acids (Ser-IL-8(72)), which comprise more than 90% of IL-8 protein in cell cultures. Serine 115-118 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 12457984-4 2002 Both orfvIL-10 and ovIL-10 inhibited TNF-alpha and IL-8 cytokine production from stimulated ovine macrophages and keratinocytes and IFN-gamma and GM-CSF production from peripheral blood lymphocytes. orfvil-10 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 12427122-6 2002 RESULTS: Endocytosis of LCs induced the release of interleukins (IL) IL-6, IL-8 and monocyte chemoattractant protein-1 (MCP-1); however, there was considerable variability among the six different LCs. lcs 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 12460404-6 2002 There were no significant differences in IL-8 levels before and after treatment in the PE group, but the IL-8 level was significantly lower after treatment in the PE+CHDF group. chdf 166-170 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 12457984-4 2002 Both orfvIL-10 and ovIL-10 inhibited TNF-alpha and IL-8 cytokine production from stimulated ovine macrophages and keratinocytes and IFN-gamma and GM-CSF production from peripheral blood lymphocytes. ovil-10 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 12215436-4 2002 PGE(2) (50 nm) attenuated LPS-induced mRNA and protein expression of chemokines including monocyte chemoattractant protein-1, interleukin-8, macrophage inflammatory protein-1alpha and -1beta, and interferon-inducible protein-10. Prostaglandins E 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 12427973-4 2002 The proangiogenic N-terminal fragment mini-TyrRS has IL-8-like cytokine activity that, like other CXC cytokines, depends on a Glu-Leu-Arg motif. Glutamic Acid 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 12427973-4 2002 The proangiogenic N-terminal fragment mini-TyrRS has IL-8-like cytokine activity that, like other CXC cytokines, depends on a Glu-Leu-Arg motif. Leucine 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 12427973-4 2002 The proangiogenic N-terminal fragment mini-TyrRS has IL-8-like cytokine activity that, like other CXC cytokines, depends on a Glu-Leu-Arg motif. Arginine 134-137 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 12457713-7 2002 Stimulations of cAMP with NaF or forskolin were the same as in control cells. Cyclic AMP 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 12427655-5 2002 Reconstitution studies demonstrated that the oleic and linoleic acids associated with E-LDL are particularly effective IL-8 inducers. oleic 45-50 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12427655-5 2002 Reconstitution studies demonstrated that the oleic and linoleic acids associated with E-LDL are particularly effective IL-8 inducers. Linoleic Acids 55-69 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12427655-7 2002 CONCLUSION: IL-8 is required for rolling monocytes to adhere firmly to the endothelium; thus, the findings reveal a link between subendothelial entrapment of LDL, cleavage of cholesterol esters, and monocyte recruitment into the lesion. Cholesterol Esters 175-193 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 12415153-1 2002 Lithium sodium aluminium fluoride was obtained as a white powder by melting a stoichiometric mixture of AlF(3), NaF and LiF at 1223 K, and then cooling to 923 K and sintering at this temperature for 4 h. The ab initio crystal structure determination was carried out using X-ray powder diffraction techniques. lithium sodium aluminium fluoride 0-33 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 12485902-4 2002 Thalidomide inhibited interleukin (IL) 1beta-induced NFkappaB transcriptional activation and IL-8 production in Caco-2 colon cancer cells. Thalidomide 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 12485855-0 2002 Activation of the p38 MAPK and ERK1/2 pathways is required for Fas-induced IL-8 production in colonic epithelial cells. ammonium ferrous sulfate 63-66 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 12149127-1 2002 Sphingosine 1-phosphate (S1P), a metabolite of sphingomyelin degradation, stimulates interleukin-8 (IL-8) secretion in human bronchial epithelial (Beas-2B) cells. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 85-98 12149127-1 2002 Sphingosine 1-phosphate (S1P), a metabolite of sphingomyelin degradation, stimulates interleukin-8 (IL-8) secretion in human bronchial epithelial (Beas-2B) cells. sphingosine 1-phosphate 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 12208470-5 2002 The Ang II type 1 receptor (AT1R) antagonist candesartan, but not the Ang II type 2 receptor (AT2R) antagonist PD123319, significantly blocked Ang II-induced IL-8 production. candesartan 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 12379708-7 2002 IL-8 expression by TNF-alpha was inhibited when two survival signals, nuclear factor kappaB (NF-kappaB) and phosphatidylinositol 3-kinase (PI3K)/Akt, were inhibited by a mutant form of inhibitor of NF-kappaB (IkappaB); by dominant negative (kinase-dead) Akt; or by treatment with LY 294002, an inhibitor of PI3K. ikappab 209-216 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12208470-6 2002 Addition of fluvastatin decreased the basal and Ang II-induced IL-8 production in VSMCs in a dose (10(-8)-10(-5) mol/l)-dependent manner with a decrease in IL-8 mRNA accumulation. Fluvastatin 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 12208470-6 2002 Addition of fluvastatin decreased the basal and Ang II-induced IL-8 production in VSMCs in a dose (10(-8)-10(-5) mol/l)-dependent manner with a decrease in IL-8 mRNA accumulation. Fluvastatin 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 12208470-7 2002 The effect of fluvastatin on IL-8 production was completely reversed in the presence of mevalonate or geranylgeranyl-pyrophosphate, but not in the presence of squalene or farnesyl-pyrophosphate. Fluvastatin 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 12208470-7 2002 The effect of fluvastatin on IL-8 production was completely reversed in the presence of mevalonate or geranylgeranyl-pyrophosphate, but not in the presence of squalene or farnesyl-pyrophosphate. Mevalonic Acid 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 12208470-7 2002 The effect of fluvastatin on IL-8 production was completely reversed in the presence of mevalonate or geranylgeranyl-pyrophosphate, but not in the presence of squalene or farnesyl-pyrophosphate. geranylgeranyl pyrophosphate 102-130 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 12208470-8 2002 Lipophilic cerivastatin also significantly decreased IL-8 production, while hydrophilic pravastatin showed no effect on IL-8 levels. cerivastatin 11-23 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 12208470-9 2002 In conclusion, we demonstrated for the first time that Ang II increased IL-8 production and fluvastatin decreased the basal and Ang II-induced IL-8 production in human VSMCs. Fluvastatin 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 12482390-3 2002 Using sensitive ELISAs, we found that Na(2)SO(3) induces the total (intra- and extracellular fractions) production of interleukin-12 (IL-12) and IL-8 but not TNF-alpha, IL-1alpha, or IL-4. sodium sulfite 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 12379708-7 2002 IL-8 expression by TNF-alpha was inhibited when two survival signals, nuclear factor kappaB (NF-kappaB) and phosphatidylinositol 3-kinase (PI3K)/Akt, were inhibited by a mutant form of inhibitor of NF-kappaB (IkappaB); by dominant negative (kinase-dead) Akt; or by treatment with LY 294002, an inhibitor of PI3K. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 280-289 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12464972-3 2002 Polaprezinc and zinc sulphate inhibited IL-8 production by MKN 45 cells in response to stimulation with H pylori water extract (HPE) in a dose-dependent manner from 10(-7) M to 10(-5) M. In addition, the expression of CD11b and CD18 on PMN and PMN-dependent adhesion to endothelial cells elicited by HPE was inhibited by polaprezinc and zinc sulphate in a concentration-dependent manner. Zinc Sulfate 16-29 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 12464972-3 2002 Polaprezinc and zinc sulphate inhibited IL-8 production by MKN 45 cells in response to stimulation with H pylori water extract (HPE) in a dose-dependent manner from 10(-7) M to 10(-5) M. In addition, the expression of CD11b and CD18 on PMN and PMN-dependent adhesion to endothelial cells elicited by HPE was inhibited by polaprezinc and zinc sulphate in a concentration-dependent manner. Water 113-118 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 12464972-3 2002 Polaprezinc and zinc sulphate inhibited IL-8 production by MKN 45 cells in response to stimulation with H pylori water extract (HPE) in a dose-dependent manner from 10(-7) M to 10(-5) M. In addition, the expression of CD11b and CD18 on PMN and PMN-dependent adhesion to endothelial cells elicited by HPE was inhibited by polaprezinc and zinc sulphate in a concentration-dependent manner. 1-(3-Methoxy-4-hydroxyphenyl)-2-[2-hydroxy-3-methoxy-5-[4-(3-methoxy-4-hydroxyphenyl)-3,7-dioxabicyclo[3.3.0]octane-8-yl]phenyl]-3-hydroxy-1-propanone 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 12464972-3 2002 Polaprezinc and zinc sulphate inhibited IL-8 production by MKN 45 cells in response to stimulation with H pylori water extract (HPE) in a dose-dependent manner from 10(-7) M to 10(-5) M. In addition, the expression of CD11b and CD18 on PMN and PMN-dependent adhesion to endothelial cells elicited by HPE was inhibited by polaprezinc and zinc sulphate in a concentration-dependent manner. Zinc Sulfate 337-350 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 12482390-6 2002 Despite the fact that Na(2)SO(3) was found to increase IL-8 production, it does not induce neutrophil chemotaxis in vitro. sodium sulfide 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 12455180-5 2002 Protec induced only a moderate production of IL-8 (1.6 fold) and IL-10 (2.3 fold) while Chizukit N caused only a moderate increase in IL-10 production (1.4 fold). lisofylline 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 12414893-7 2002 IL-8 production by HCG was not affected by inhibitors of protein kinases A and C. In contrast, this stimulation was attenuated by D-mannose, which inhibits binding to C-type lectins. Mannose 130-139 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12384994-6 2002 In vitro, IL-8 treated fibroblasts demonstrated an increase in GJIC by scrape loading compared to saline treated controls. Sodium Chloride 98-104 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 12402194-3 2002 Culture supernatants of 6 wild-type strains of S. pneumoniae, shown to contain choline-binding protein A (CbpA; clades A and B), induced release of chemokine CXCL8 from the human alveolar epithelial cell line A549, whereas a CbpA deletion mutant elicited significantly reduced CXCL8 release, compared with that of its isogenic parent (P<.01). Choline 79-86 C-X-C motif chemokine ligand 8 Homo sapiens 158-163 12384994-7 2002 In vivo, IL-8 treated PVA sponges demonstrated a decrease in cell density and an increase in vascularization compared to saline controls by H&E staining. Polyvinyl Alcohol 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 12384994-7 2002 In vivo, IL-8 treated PVA sponges demonstrated a decrease in cell density and an increase in vascularization compared to saline controls by H&E staining. Sodium Chloride 121-127 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 12231210-4 2002 SP had a significant effect in that it decreased RA synovial tissue explant secretion of IL-8 (22%), GROalpha (55%), and monocyte chemotactic protein-1 (MCP-1) (42%) (P < 0.05). Sulfapyridine 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 12429722-5 2002 In addition IL-12 induces the de novo synthesis and production of IL-8 and tumor necrosis factor alpha (TNF-alpha) in a calcium- and ROM-dependent manner. Calcium 120-127 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 12296854-7 2002 Moreover, blocking the activation of NF-kappaB by MG-132 or antisense p50 oligonucleotide transfection resulted in down-regulated expression of chemokines such as CXCL1, CXCL8, and CCL2 in BFT-stimulated HT-29 cells. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 170-175 12296854-7 2002 Moreover, blocking the activation of NF-kappaB by MG-132 or antisense p50 oligonucleotide transfection resulted in down-regulated expression of chemokines such as CXCL1, CXCL8, and CCL2 in BFT-stimulated HT-29 cells. Oligonucleotides 74-89 C-X-C motif chemokine ligand 8 Homo sapiens 170-175 12231210-8 2002 These data suggest that SASP may function to reduce inflammation in RA through the effects of its metabolite SP to reduce the secretion of the inflammatory chemokines IL-8, GROalpha, and MCP-1. Sulfapyridine 26-28 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 12238566-0 2002 A green tea-derived polyphenol, epigallocatechin-3-gallate, inhibits IkappaB kinase activation and IL-8 gene expression in respiratory epithelium. Polyphenols 20-30 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 12238566-0 2002 A green tea-derived polyphenol, epigallocatechin-3-gallate, inhibits IkappaB kinase activation and IL-8 gene expression in respiratory epithelium. epigallocatechin gallate 32-58 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 12238566-3 2002 Herein we determined the effects of epigallocatechin-3-gallate (EGCG), a green tea-derived polyphenol, on tumor necrosis factor-alpha (TNF-alpha)-mediated expression of the IL-8 gene in A549 cells. epigallocatechin gallate 36-62 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12238566-3 2002 Herein we determined the effects of epigallocatechin-3-gallate (EGCG), a green tea-derived polyphenol, on tumor necrosis factor-alpha (TNF-alpha)-mediated expression of the IL-8 gene in A549 cells. epigallocatechin gallate 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12238566-3 2002 Herein we determined the effects of epigallocatechin-3-gallate (EGCG), a green tea-derived polyphenol, on tumor necrosis factor-alpha (TNF-alpha)-mediated expression of the IL-8 gene in A549 cells. Polyphenols 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 12683216-0 2002 Modulation of interleukin-8 receptor expression by lipopolysaccharide (LPS) and phorbol myristate acetate (PMA) in human peripheral monocytes--a preliminary study. Tetradecanoylphorbol Acetate 80-105 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 12683216-0 2002 Modulation of interleukin-8 receptor expression by lipopolysaccharide (LPS) and phorbol myristate acetate (PMA) in human peripheral monocytes--a preliminary study. Tetradecanoylphorbol Acetate 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 12238566-4 2002 EGCG inhibited TNF-alpha-mediated IL-8 gene expression in a dose response manner, as measured by ELISA and Northern blot analysis. epigallocatechin gallate 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 12683216-3 2002 We found that two very known modulators, lipopolysaccharide (LPS) in presence of homologous serum and Phorbol myristate acetate (PMA) resulted in induction of IL-8 receptor by 100-120% and 75-125% respectively within 1 h in monocytes. Tetradecanoylphorbol Acetate 102-127 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 12238566-5 2002 This effect appears to primarily involve inhibition of IL-8 transcription because EGCG inhibited TNF-alpha-mediated activation of the IL-8 promoter in cells transiently transfected with an IL-8 promoter-luciferase reporter plasmid. epigallocatechin gallate 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 12683216-3 2002 We found that two very known modulators, lipopolysaccharide (LPS) in presence of homologous serum and Phorbol myristate acetate (PMA) resulted in induction of IL-8 receptor by 100-120% and 75-125% respectively within 1 h in monocytes. Tetradecanoylphorbol Acetate 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 12683216-4 2002 Based on the inhibitory effect of cycloheximide, actinomycin-D we may suggest that PMA and LPS could upregulate IL-8 receptor in monocytes through denovo protein synthesis. Cycloheximide 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 12238566-5 2002 This effect appears to primarily involve inhibition of IL-8 transcription because EGCG inhibited TNF-alpha-mediated activation of the IL-8 promoter in cells transiently transfected with an IL-8 promoter-luciferase reporter plasmid. epigallocatechin gallate 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 12683216-4 2002 Based on the inhibitory effect of cycloheximide, actinomycin-D we may suggest that PMA and LPS could upregulate IL-8 receptor in monocytes through denovo protein synthesis. Dactinomycin 49-62 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 12683216-4 2002 Based on the inhibitory effect of cycloheximide, actinomycin-D we may suggest that PMA and LPS could upregulate IL-8 receptor in monocytes through denovo protein synthesis. Tetradecanoylphorbol Acetate 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 12683216-5 2002 Prior incubation of polymixin B and anti-CD-14 antibody to the monocytes and subsequent stimulation of the cells with ser.act.LPS resulted in > 90% inhibition of IL-8 binding. Serine 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 12683216-8 2002 Chemical cross-linking of the IL-8 receptor with 125I labelled IL-8 in the ser.act.LPS and PMA stimulated cells-indicated that the signals at 59 kD were considerably increased with respect to control. Serine 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 12683216-8 2002 Chemical cross-linking of the IL-8 receptor with 125I labelled IL-8 in the ser.act.LPS and PMA stimulated cells-indicated that the signals at 59 kD were considerably increased with respect to control. Serine 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 12418602-2 2002 Commonly, weekly or twice monthly rinsing procedures using neutral 0.2% NaF solutions have been used in schools or institutions in areas with low fluoride concentrations in the drinking water. Fluorides 146-154 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 12238566-5 2002 This effect appears to primarily involve inhibition of IL-8 transcription because EGCG inhibited TNF-alpha-mediated activation of the IL-8 promoter in cells transiently transfected with an IL-8 promoter-luciferase reporter plasmid. epigallocatechin gallate 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 12683216-9 2002 A correlation between LPS and ser.act.LPS induced upregulation of IL-8 receptor expression has been shown. Serine 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 12238566-7 2002 We conclude that EGCG is a potent inhibitor of IL-8 gene expression in vitro. epigallocatechin gallate 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12433059-5 2002 However, beta-glucan itself induced the production of significant amounts of IL-8 and TF. beta-Glucans 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 77-88 12368623-7 2002 RESULTS: Clarithromycin and prednisolone each produced significant reductions in interleukin-5, interleukin-8, and granulocyte-macrophage colony-stimulating factor production. Clarithromycin 9-23 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 12364456-7 2002 Treatment of placental, amnion, and choriodecidual tissues with both 15d-PGJ(2) and troglitazone significantly reduced the release of lipopolysaccharide-stimulated IL-6, IL-8, and TNF-alpha (t test, P < 0.05). 15d-pgj 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 12364456-7 2002 Treatment of placental, amnion, and choriodecidual tissues with both 15d-PGJ(2) and troglitazone significantly reduced the release of lipopolysaccharide-stimulated IL-6, IL-8, and TNF-alpha (t test, P < 0.05). Troglitazone 84-96 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 12244149-6 2002 U87 cells treated with morphine showed significant down-regulation of IL-8 gene expression, whereas expression of the IL-8 receptor CXCR2 was reciprocally up-regulated as detected by RT-PCR. Morphine 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 12244149-7 2002 Treatment of NHAs with morphine suppressed IL-8 and macrophage-inflammatory protein-1beta gene expression, whereas expression of their receptor genes, CCR3 and CCR5, was simultaneously enhanced. Morphine 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 12368623-7 2002 RESULTS: Clarithromycin and prednisolone each produced significant reductions in interleukin-5, interleukin-8, and granulocyte-macrophage colony-stimulating factor production. Prednisolone 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 12204776-0 2002 17Beta-estradiol inhibits the adhesion of leukocytes in TNF-alpha stimulated human endothelial cells by blocking IL-8 and MCP-1 secretion, but not its transcription. Estradiol 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 12383538-6 2002 Monocyte chemoattractant protein-1 and interleukin-8 production was decreased by the antioxidant vitamin E in human umbilical vein endothelial cells treated with preeclamptic plasma, suggesting that the production of these cytokines may be regulated by signaling mechanisms sensitive to oxidative stress. Vitamin E 97-106 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 12235371-0 2002 Lipoxin A4 and aspirin-triggered 15-epi-lipoxin A4 inhibit peroxynitrite formation, NF-kappa B and AP-1 activation, and IL-8 gene expression in human leukocytes. lipoxin A4 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 12235371-0 2002 Lipoxin A4 and aspirin-triggered 15-epi-lipoxin A4 inhibit peroxynitrite formation, NF-kappa B and AP-1 activation, and IL-8 gene expression in human leukocytes. Aspirin 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 12235371-0 2002 Lipoxin A4 and aspirin-triggered 15-epi-lipoxin A4 inhibit peroxynitrite formation, NF-kappa B and AP-1 activation, and IL-8 gene expression in human leukocytes. lipoxin A4 33-50 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 12235371-2 2002 Recent studies indicate that peroxynitrite (ONOO(-)) may function as an intracellular signal for the production of IL-8, a potent proinflammatory cytokine in human leukocytes. Peroxynitrous Acid 29-42 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 12235371-2 2002 Recent studies indicate that peroxynitrite (ONOO(-)) may function as an intracellular signal for the production of IL-8, a potent proinflammatory cytokine in human leukocytes. onoo(-) 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 12235371-3 2002 In this study, we evaluated the impact of the metabolically stable analogues of LXA(4)/ATL on lipopolysaccharide (LPS)-induced ONOO(-) formation and ONOO(-)-mediated IL-8 gene expression in human leukocytes. onoo 149-153 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 12542924-14 2002 Addition of POLY and TAU led to comparable low IL-8 gradients with concomitant low PMN transmigration. poly 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12542924-14 2002 Addition of POLY and TAU led to comparable low IL-8 gradients with concomitant low PMN transmigration. taurolidine 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12207111-0 2002 In vitro effect of fluticasone propionate on interleukin 8 production by monocytes obtained from patients affected by moderate-severe allergic asthma. Fluticasone 19-41 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 12207111-2 2002 The aim of this study was to evaluate the effect of fluticasone propionate (FP), a corticosteroid with potent anti-inflammatory activity, on the in vitro release of IL-8 by monocytes obtained from asthmatic patients. Fluticasone 52-74 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 12216086-0 2002 Curcumin inhibits interleukin 8 production and enhances interleukin 8 receptor expression on the cell surface:impact on human pancreatic carcinoma cell growth by autocrine regulation. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 12216086-0 2002 Curcumin inhibits interleukin 8 production and enhances interleukin 8 receptor expression on the cell surface:impact on human pancreatic carcinoma cell growth by autocrine regulation. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 12216086-5 2002 RESULTS: The constitutive production of IL-8 was inhibited by curcumin at concentrations of 10-100 microM in a dose dependent manner. Curcumin 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 12218154-8 2002 While AP-1 is involved in regulating the IL-1alpha-induced expression of IL-8, but not MCP-1, alprazolam potentiated the binding of c-Jun/c-Fos to the AP-1 oligonucleotide probe. Alprazolam 94-104 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 12218154-8 2002 While AP-1 is involved in regulating the IL-1alpha-induced expression of IL-8, but not MCP-1, alprazolam potentiated the binding of c-Jun/c-Fos to the AP-1 oligonucleotide probe. Oligonucleotides 156-171 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 12216086-9 2002 The investigation of expression in IL-8 receptors, CXCR1 and CXCR2, revealed that the expression of both receptors was enhanced remarkably by curcumin. Curcumin 142-150 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 12218154-9 2002 These results show that the inhibition of IL-1alpha-mediated MCP-1 production by alprazolam is mainly due to inhibition of c-Rel/p65 and c-Rel/p50 binding to the MCP-1 promoter region, since alprazolam did not affect the IL-1alpha-mediated activation of NF-kappaB (p50/p65) or AP-1 (c-Jun/c-Fos) binding to the IL-8 promoter region. Alprazolam 81-91 C-X-C motif chemokine ligand 8 Homo sapiens 311-315 12216086-11 2002 These results suggest that curcumin inhibits IL-8-induced receptor internalization. Curcumin 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 12216086-12 2002 CONCLUSIONS: The authors concluded that curcumin contributed not only to the inhibition of IL-8 production but also to signal transduction through IL-8 receptors. Curcumin 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 12216086-12 2002 CONCLUSIONS: The authors concluded that curcumin contributed not only to the inhibition of IL-8 production but also to signal transduction through IL-8 receptors. Curcumin 40-48 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 12216086-13 2002 These data suggest that curcumin reduces numerous IL-8 bioactivities that contribute to tumor growth and carcinoma cell viability. Curcumin 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 12216086-14 2002 From this point of view, curcumin is a potent anticancer agent that inhibits the production of proinflammatory cytokines, including IL-8, by tumor cells. Curcumin 25-33 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 12393170-0 2002 Polycyclic aromatic hydrocarbons induce IL-8 expression through nuclear factor kappaB activation in A549 cell line. Polycyclic Aromatic Hydrocarbons 0-32 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 12207893-4 2002 EM-X inhibited the release of IL-8 at the transcriptional level in A549 cells. em-x 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 12393170-4 2002 Asbestos exposure and particulate air pollution have been reported to stimulate the expression of IL-8 and to induce NF-kappaB activation. Asbestos 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 12393170-5 2002 However, it is unknown whether polycyclic aromatic hydrocarbons (PAH), mainly existed in most airborne particulates, can separately induce IL-8 expression. Polycyclic Aromatic Hydrocarbons 31-63 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 12393170-5 2002 However, it is unknown whether polycyclic aromatic hydrocarbons (PAH), mainly existed in most airborne particulates, can separately induce IL-8 expression. Polycyclic Aromatic Hydrocarbons 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 12393170-6 2002 In the present study, we investigated the effect of benzo(a)pyrene (B[a]P) and 1-nitropyrene (1-NP), two representative PAH, on IL-8 expression using ELISA and Northern blot analysis. Benzo(a)pyrene 52-66 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 12393170-6 2002 In the present study, we investigated the effect of benzo(a)pyrene (B[a]P) and 1-nitropyrene (1-NP), two representative PAH, on IL-8 expression using ELISA and Northern blot analysis. Benzo(a)pyrene 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 12393170-6 2002 In the present study, we investigated the effect of benzo(a)pyrene (B[a]P) and 1-nitropyrene (1-NP), two representative PAH, on IL-8 expression using ELISA and Northern blot analysis. 1-nitropyrene 79-92 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 12393170-6 2002 In the present study, we investigated the effect of benzo(a)pyrene (B[a]P) and 1-nitropyrene (1-NP), two representative PAH, on IL-8 expression using ELISA and Northern blot analysis. 1-nitropyrene 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 12393170-6 2002 In the present study, we investigated the effect of benzo(a)pyrene (B[a]P) and 1-nitropyrene (1-NP), two representative PAH, on IL-8 expression using ELISA and Northern blot analysis. Polycyclic Aromatic Hydrocarbons 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 12393170-8 2002 We have assessed the effect of adenovirus-mediated overexpression of the NF-kappaB inhibitor, IkappaBalpha on PAH-induced IL-8 expression in A549 cell line. Polycyclic Aromatic Hydrocarbons 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 12393170-12 2002 This suggests that PAH-induced IL-8 gene regulation may be mediated by NF-kappaB. Polycyclic Aromatic Hydrocarbons 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 12393170-13 2002 These data indicate that PAH alone, either B[a]P or 1-NP, is sufficient to stimulate NF-kappaB activation and IL-8 transcription. Polycyclic Aromatic Hydrocarbons 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 12176755-6 2002 Similarly, cross-linked MAbVLA-4 or VCAM-1 augmented Ca(2+)-mediated IL-8 secretion from THP-1 monocytes and was completely abolished by exposure to CsCl, an I(ir) blocker. cesium chloride 149-153 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 12169581-5 2002 Furthermore, the COX substrate arachidonic acid and exogenous prostaglandin E(2) both increased IL-8 release in A549 cells. Arachidonic Acid 31-47 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 12169581-5 2002 Furthermore, the COX substrate arachidonic acid and exogenous prostaglandin E(2) both increased IL-8 release in A549 cells. Dinoprostone 62-80 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 12169581-0 2002 Bradykinin increases IL-8 generation in airway epithelial cells via COX-2-derived prostanoids. Prostaglandins 82-93 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 12169581-2 2002 Here we tested the hypothesis that bradykinin, an inflammatory mediator and chloride secretagogue, would increase IL-8 generation in airway epithelial cells through autocrine generation of endogenous prostanoids. Chlorides 76-84 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 12169581-2 2002 Here we tested the hypothesis that bradykinin, an inflammatory mediator and chloride secretagogue, would increase IL-8 generation in airway epithelial cells through autocrine generation of endogenous prostanoids. Prostaglandins 200-211 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 12169581-3 2002 Bradykinin increased IL-8 generation in both a non-cystic fibrosis (A549) and cystic fibrosis epithelial cell line (CFTE29) that was inhibited by the nonselective cyclooxygenase (COX) inhibitor indomethacin and the COX-2 selective inhibitor NS-398. Indomethacin 194-206 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 12169581-3 2002 Bradykinin increased IL-8 generation in both a non-cystic fibrosis (A549) and cystic fibrosis epithelial cell line (CFTE29) that was inhibited by the nonselective cyclooxygenase (COX) inhibitor indomethacin and the COX-2 selective inhibitor NS-398. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 241-247 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 12213589-7 2002 Both TNF-alpha and the oxidant, hydrogen peroxide (H2O2) alter histone acetylation/deacetylation, and the activation of NF-kappaB and AP-1, leading to the release of the pro-inflammatory cytokine interleukin-8 (IL-8) in human alveolar epithelial cells (A549). Hydrogen Peroxide 32-49 C-X-C motif chemokine ligand 8 Homo sapiens 196-209 12213589-7 2002 Both TNF-alpha and the oxidant, hydrogen peroxide (H2O2) alter histone acetylation/deacetylation, and the activation of NF-kappaB and AP-1, leading to the release of the pro-inflammatory cytokine interleukin-8 (IL-8) in human alveolar epithelial cells (A549). Hydrogen Peroxide 32-49 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 12213589-7 2002 Both TNF-alpha and the oxidant, hydrogen peroxide (H2O2) alter histone acetylation/deacetylation, and the activation of NF-kappaB and AP-1, leading to the release of the pro-inflammatory cytokine interleukin-8 (IL-8) in human alveolar epithelial cells (A549). Hydrogen Peroxide 51-55 C-X-C motif chemokine ligand 8 Homo sapiens 196-209 12213589-7 2002 Both TNF-alpha and the oxidant, hydrogen peroxide (H2O2) alter histone acetylation/deacetylation, and the activation of NF-kappaB and AP-1, leading to the release of the pro-inflammatory cytokine interleukin-8 (IL-8) in human alveolar epithelial cells (A549). Hydrogen Peroxide 51-55 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 12213589-8 2002 Pharmacological inhibition of HDAC leads to the increased HAT activity, AP-1 and NF-kappaB activation, and IL-8 release by H2O2 or TNF-alpha treatments. Hydrogen Peroxide 123-127 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 12213594-4 2002 Moreover, preincubation of HUVEC with 10 ng/mL TcdB-10463 reduced TNF-alpha-related expression of interleukin-8 (IL-8), TNF-receptor associated factor-2 (TRAF2), and human inhibitor of apoptosis protein 1 (hIAP1)-mRNA. trimethylaminocarboxyldihydroboran 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 12213594-4 2002 Moreover, preincubation of HUVEC with 10 ng/mL TcdB-10463 reduced TNF-alpha-related expression of interleukin-8 (IL-8), TNF-receptor associated factor-2 (TRAF2), and human inhibitor of apoptosis protein 1 (hIAP1)-mRNA. trimethylaminocarboxyldihydroboran 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 12176910-9 2002 The removal of TLR2 lipopeptide components from LPS by phenol re-extraction substantially reduced both the IL-8 and superoxide response of the stimulated neutrophils, indicating that, unlike monocytes, the neutrophil response is preferentially directed to TLR2 ligands. Phenol 55-61 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 12193739-4 2002 HMC-1-induced IL-8 release was significantly reduced by the tryptase inhibitors GW-45 and GW-58 (90 and 87%, respectively, at an optimal concentration) but not by anti-stem cell factor, anti-TNF-alpha, or anti-IFN-gamma neutralizing Abs or by the antihistamine drugs pyrilamine and cimetidine. Cimetidine 282-292 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 12607189-6 2002 RESULTS: Histamine increased the production of IL-1, IL-6 and IL-8, and ICAM-1 expression. Histamine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 12607189-8 2002 The antiH-1, emedastine, significantly reduced H-induced production of IL-1, IL-6 and IL-8, while azelastine reduced only IL-1. emedastine 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 12193739-4 2002 HMC-1-induced IL-8 release was significantly reduced by the tryptase inhibitors GW-45 and GW-58 (90 and 87%, respectively, at an optimal concentration) but not by anti-stem cell factor, anti-TNF-alpha, or anti-IFN-gamma neutralizing Abs or by the antihistamine drugs pyrilamine and cimetidine. glycyltryptophan 80-82 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 12353856-0 2002 Local release of human neutrophil lipocalin (HNL), IL-8, and TNF-alpha is decreased as response to topical prednisolone treatment in distal ulcerative colitis and proctitis. Prednisolone 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 12193669-9 2002 Dexamethasone inhibited IL-8 secretion by 34 +/- 8% in children and by 41 +/- 3% in adults but had no effect on infant PBMC. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 12225373-5 2002 Stimulation with zymosan and LPS readily induced interleukin (IL)-6 and IL-8 cytokine production in the placenta cultures, whereas TLR2 and TLR4 mRNA and protein expression remained at the same high level as in unstimulated explants. Zymosan 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 12193739-4 2002 HMC-1-induced IL-8 release was significantly reduced by the tryptase inhibitors GW-45 and GW-58 (90 and 87%, respectively, at an optimal concentration) but not by anti-stem cell factor, anti-TNF-alpha, or anti-IFN-gamma neutralizing Abs or by the antihistamine drugs pyrilamine and cimetidine. gw-58 90-95 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 12193739-4 2002 HMC-1-induced IL-8 release was significantly reduced by the tryptase inhibitors GW-45 and GW-58 (90 and 87%, respectively, at an optimal concentration) but not by anti-stem cell factor, anti-TNF-alpha, or anti-IFN-gamma neutralizing Abs or by the antihistamine drugs pyrilamine and cimetidine. Pyrilamine 267-277 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 12193669-11 2002 However, the inhibitory effects of steroids on IL-8 secretion are absent in infants, which may partly explain why they develop more severe bronchiolitis, and why steroid therapy is unsuccessful in clinical practice. Steroids 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12193669-11 2002 However, the inhibitory effects of steroids on IL-8 secretion are absent in infants, which may partly explain why they develop more severe bronchiolitis, and why steroid therapy is unsuccessful in clinical practice. Steroids 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 12201814-8 2002 injections of prostaglandin 9 days apart, IL-8 gene expression at oestrus was significantly lower than it was at natural oestrus. Prostaglandins 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 12176048-1 2002 Human osteoblast-like cells (hOB) stimulated by monosodium urate monohydrate (MSUM) or calcium pyrophosphate dihydrate (CPPD) microcrystals produce the neutrophil chemoattractant IL-8. Uric Acid 48-76 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 12208513-1 2002 In this report we explored the effects of proteasome inhibitors (MG132, aLLN, lactacystin and MG262) on interleukin-8 (IL-8) induction. MG 262 94-99 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12208513-3 2002 The stimulating effects on IL-8 promoter and AP-1 were reduced by N-acetylcysteine, glutathione, diphenyleneiodonium, rotenone and antimycin A. Acetylcysteine 66-82 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 12208513-3 2002 The stimulating effects on IL-8 promoter and AP-1 were reduced by N-acetylcysteine, glutathione, diphenyleneiodonium, rotenone and antimycin A. Glutathione 84-95 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 12208513-3 2002 The stimulating effects on IL-8 promoter and AP-1 were reduced by N-acetylcysteine, glutathione, diphenyleneiodonium, rotenone and antimycin A. diphenyleneiodonium 97-116 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 12208513-3 2002 The stimulating effects on IL-8 promoter and AP-1 were reduced by N-acetylcysteine, glutathione, diphenyleneiodonium, rotenone and antimycin A. Rotenone 118-126 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 12208513-3 2002 The stimulating effects on IL-8 promoter and AP-1 were reduced by N-acetylcysteine, glutathione, diphenyleneiodonium, rotenone and antimycin A. Antimycin A 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 12208513-5 2002 These results suggest that ROS production by proteasome inhibitors leads to AP-1 activation, which in the absence of NF-kappa B activation still transactivates IL-8 gene expression. Reactive Oxygen Species 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 12215676-5 2002 In the present study, we found that Na(2)SO(3) (0.01-10 mM) induces tyrosine phosphorylation events and interleukin-8 production in human epithelial lung A549 cells. sodium sulfite 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 12215678-7 2002 There were differences between the aliphatic hydrocarbons with respect to their effects on IL-8 release. Hydrocarbons 45-57 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 12215678-8 2002 IL-8 concentration was increased significantly by 3- to 10-fold, with the highest increase found after exposure to hydrocarbons in the C9-C13 range. Hydrocarbons 115-127 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12077146-6 2002 On the other hand, cells expressing all single, double, or triple histidine-substituted CXCR1 demonstrated high affinity binding to interleukin 8 in the presence and absence of metal ions. Histidine 66-75 C-X-C motif chemokine ligand 8 Homo sapiens 132-145 12208513-1 2002 In this report we explored the effects of proteasome inhibitors (MG132, aLLN, lactacystin and MG262) on interleukin-8 (IL-8) induction. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 65-70 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 12208513-1 2002 In this report we explored the effects of proteasome inhibitors (MG132, aLLN, lactacystin and MG262) on interleukin-8 (IL-8) induction. allosamine 72-76 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 12208513-1 2002 In this report we explored the effects of proteasome inhibitors (MG132, aLLN, lactacystin and MG262) on interleukin-8 (IL-8) induction. allosamine 72-76 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12208513-1 2002 In this report we explored the effects of proteasome inhibitors (MG132, aLLN, lactacystin and MG262) on interleukin-8 (IL-8) induction. lactacystin 78-89 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 12208513-1 2002 In this report we explored the effects of proteasome inhibitors (MG132, aLLN, lactacystin and MG262) on interleukin-8 (IL-8) induction. lactacystin 78-89 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12208513-1 2002 In this report we explored the effects of proteasome inhibitors (MG132, aLLN, lactacystin and MG262) on interleukin-8 (IL-8) induction. MG 262 94-99 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 12176048-1 2002 Human osteoblast-like cells (hOB) stimulated by monosodium urate monohydrate (MSUM) or calcium pyrophosphate dihydrate (CPPD) microcrystals produce the neutrophil chemoattractant IL-8. Uric Acid 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 12176048-1 2002 Human osteoblast-like cells (hOB) stimulated by monosodium urate monohydrate (MSUM) or calcium pyrophosphate dihydrate (CPPD) microcrystals produce the neutrophil chemoattractant IL-8. Calcium Pyrophosphate 87-118 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 12176048-1 2002 Human osteoblast-like cells (hOB) stimulated by monosodium urate monohydrate (MSUM) or calcium pyrophosphate dihydrate (CPPD) microcrystals produce the neutrophil chemoattractant IL-8. Calcium Pyrophosphate 120-124 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 12297109-5 2002 Using reverse transcriptase-polymerase chain reaction (RT-PCR), immunoprecipitation and western blot analysis, we report that the early signalling events triggered by the hIL-17 involved tyrosyl phosphorylation of proteins and increased the levels of IL-6, IL-8 and MCP-1 in a dose-dependent manner. cyclo(tyrosyl-tyrosyl) 187-194 C-X-C motif chemokine ligand 8 Homo sapiens 257-261 12151316-1 2002 In this study, we investigated the effects of proteasome inhibibors (MG132 and lactacystin) on interleukin (IL)-8 induction. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 95-113 12039947-0 2002 Phospholipase D activation by sphingosine 1-phosphate regulates interleukin-8 secretion in human bronchial epithelial cells. sphingosine 1-phosphate 30-53 C-X-C motif chemokine ligand 8 Homo sapiens 64-77 12039947-7 2002 Inhibition of 12-O-tetradecanoyl-phorbol-13-acetate-stimulated IL-8 production by 1-butanol further strengthened this observation. Tetradecanoylphorbol Acetate 14-51 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 12039947-7 2002 Inhibition of 12-O-tetradecanoyl-phorbol-13-acetate-stimulated IL-8 production by 1-butanol further strengthened this observation. 1-Butanol 82-91 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 18968742-7 2002 Potential interference from dissolved silica and Fe(III) is eliminated by the addition of NaF to the sample. Silicon Dioxide 38-44 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 18968742-7 2002 Potential interference from dissolved silica and Fe(III) is eliminated by the addition of NaF to the sample. ferric sulfate 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 12107048-5 2002 The suppressive effect of amiloride on endotoxin-induced IL-8 production was associated with a decreased accumulation of IL-8 mRNA. Amiloride 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 12107048-5 2002 The suppressive effect of amiloride on endotoxin-induced IL-8 production was associated with a decreased accumulation of IL-8 mRNA. Amiloride 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 12151316-1 2002 In this study, we investigated the effects of proteasome inhibibors (MG132 and lactacystin) on interleukin (IL)-8 induction. lactacystin 79-90 C-X-C motif chemokine ligand 8 Homo sapiens 95-113 12151316-2 2002 In human epithelial A549 cells, MG132 and lactacystin induced IL-8 release within the range of 0.1-30 microM. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 12151316-2 2002 In human epithelial A549 cells, MG132 and lactacystin induced IL-8 release within the range of 0.1-30 microM. lactacystin 42-53 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 12151316-3 2002 The effect of MG132 resulted from IL-8 gene transcription and was blocked by PD 98059, but was unaffected by GF109203X, Ro 31-8220, or SB 203580. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 12151316-4 2002 Mutational analysis of the 5" flanking region of the IL-8 gene revealed that activator protein (AP)-1-binding element, but not that element responsive to nuclear factor (NF)-IL-6 or NF-kappaB, was necessary for MG132 stimulation. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 211-216 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 12151316-7 2002 In addition, activations of the IL-8 gene and AP-1 by MG132 and lactacystin were inhibited by GSH and NAC. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 54-59 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 12151316-7 2002 In addition, activations of the IL-8 gene and AP-1 by MG132 and lactacystin were inhibited by GSH and NAC. lactacystin 64-75 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 12151316-7 2002 In addition, activations of the IL-8 gene and AP-1 by MG132 and lactacystin were inhibited by GSH and NAC. Glutathione 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 12151316-8 2002 Herein we present a novel action of proteasome inhibitors, possibly through ROS production, of targeting the upstream signaling molecules, ERK and JNK, which leads to AP-1 activation and IL-8 gene expression. ros 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 12169830-6 2002 The 50% inhibitory concentrations by DEX, BET, and HC for IL-8 release were 3.4 +/- (SE) 1.6 x 10(-9), 1.8 +/- 7.4 x 10(-8), and 1.8 +/- 0.5 x 10(-7) M, respectively. Dexamethasone 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12151344-0 2002 Expression of interleukin-8, heme oxygenase-1 and vascular endothelial growth factor in DLD-1 colon carcinoma cells exposed to pyrrolidine dithiocarbamate. pyrrolidine dithiocarbamic acid 127-154 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 12169830-6 2002 The 50% inhibitory concentrations by DEX, BET, and HC for IL-8 release were 3.4 +/- (SE) 1.6 x 10(-9), 1.8 +/- 7.4 x 10(-8), and 1.8 +/- 0.5 x 10(-7) M, respectively. Betamethasone 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 12139725-0 2002 Simultaneous induction of matrix metalloproteinase-9 and interleukin 8 by all-trans retinoic acid in human PL-21 and NB4 myeloid leukaemia cells. 2-octenal 78-83 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 12139725-0 2002 Simultaneous induction of matrix metalloproteinase-9 and interleukin 8 by all-trans retinoic acid in human PL-21 and NB4 myeloid leukaemia cells. Tretinoin 84-97 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 12139725-8 2002 ATRA can induce interleukin 8 (IL-8) in APL cells. Tretinoin 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 12139725-8 2002 ATRA can induce interleukin 8 (IL-8) in APL cells. Tretinoin 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 12139725-9 2002 IL-8, chemokine for neutrophils and a potent inducer of MMP-9, was also induced by ATRA in PL-21 cells. Tretinoin 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Dexamethasone 58-71 C-X-C motif chemokine ligand 8 Homo sapiens 203-216 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Dexamethasone 58-71 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Dexamethasone 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 203-216 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Dexamethasone 73-76 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Betamethasone 79-92 C-X-C motif chemokine ligand 8 Homo sapiens 203-216 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Betamethasone 79-92 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Betamethasone 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 203-216 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Betamethasone 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Hydrocortisone 104-118 C-X-C motif chemokine ligand 8 Homo sapiens 203-216 12169830-1 2002 The objective of this study was to determine the doses of dexamethasone (DEX), betamethasone (BET), and hydrocortisone (HC) that effectively inhibit the release of two potent proinflammatory chemokines, interleukin 8 (IL-8) and macrophage inflammatory protein alpha (MIP), from polymorphonuclear neutrophils (PMNs) of the newborn. Hydrocortisone 104-118 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 12169830-4 2002 Maximal inhibitions of IL-8 release by BET, DEX, and HC were 97, 91, and 91%, respectively. Betamethasone 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 12169830-4 2002 Maximal inhibitions of IL-8 release by BET, DEX, and HC were 97, 91, and 91%, respectively. Dexamethasone 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 12139725-12 2002 These observations suggest that ATRA can induce both MMP-9 and IL-8, but IL-8 is not involved in ATRA-induced MMP-9 expression. Tretinoin 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 12139725-13 2002 As MMP-9 can truncate and activate IL-8, simultaneous induction of MMP-9 and IL-8 by ATRA could activate leucocytes excessively, causing the hyper-inflammatory events in retinoic acid syndrome. Tretinoin 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 12139725-13 2002 As MMP-9 can truncate and activate IL-8, simultaneous induction of MMP-9 and IL-8 by ATRA could activate leucocytes excessively, causing the hyper-inflammatory events in retinoic acid syndrome. Tretinoin 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 12151344-3 2002 Here we report that pyrrolidine dithiocarbamate (PDTC) not only augmented tumor necrosis factor-alpha-induced release of IL-8, but also mediated IL-8 expression as a single stimulus. pyrrolidine dithiocarbamic acid 20-47 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 12151344-3 2002 Here we report that pyrrolidine dithiocarbamate (PDTC) not only augmented tumor necrosis factor-alpha-induced release of IL-8, but also mediated IL-8 expression as a single stimulus. pyrrolidine dithiocarbamic acid 20-47 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 12151344-3 2002 Here we report that pyrrolidine dithiocarbamate (PDTC) not only augmented tumor necrosis factor-alpha-induced release of IL-8, but also mediated IL-8 expression as a single stimulus. pyrrolidine dithiocarbamic acid 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 12151344-3 2002 Here we report that pyrrolidine dithiocarbamate (PDTC) not only augmented tumor necrosis factor-alpha-induced release of IL-8, but also mediated IL-8 expression as a single stimulus. pyrrolidine dithiocarbamic acid 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 12154423-9 2002 MEASUREMENTS AND MAIN RESULTS: In the control and tranexamic acid groups, tumor necrosis factor-alpha, IL-6, and IL-10 secretion by whole blood cell cultures were rapidly decreased, whereas IL-8 secretion was unaffected. Tranexamic Acid 50-65 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 12171898-5 2002 IL-8 has been reported to augment the progression of some human tumors; thus, we used a human IL-8 antibody, ABXIL8, in combination with anti-EGFR, ABXEGFR, to inhibit the metastasis of MDA231 tumors. abxil8 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12171898-5 2002 IL-8 has been reported to augment the progression of some human tumors; thus, we used a human IL-8 antibody, ABXIL8, in combination with anti-EGFR, ABXEGFR, to inhibit the metastasis of MDA231 tumors. abxil8 109-115 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 12165085-7 2002 T-HPMC and P-HPMC constitutively expressed IL-6 and IL-8 at both protein and mRNA level. t-hpmc 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 12165085-7 2002 T-HPMC and P-HPMC constitutively expressed IL-6 and IL-8 at both protein and mRNA level. p-hpmc 11-17 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 12165085-11 2002 These data indicate that (1) T-HPMC lines mimic the morphological and functional features of P-HPMC, (2) P-HPMC and T-HPMC constituitively produce IL-6 and IL-8, which is enhanced by hIL-1beta and hTNF-alpha and (3) HPMC in vivo may participate in the pathogenesis of benign and malignant gynaecological disease. t-hpmc 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 12165085-11 2002 These data indicate that (1) T-HPMC lines mimic the morphological and functional features of P-HPMC, (2) P-HPMC and T-HPMC constituitively produce IL-6 and IL-8, which is enhanced by hIL-1beta and hTNF-alpha and (3) HPMC in vivo may participate in the pathogenesis of benign and malignant gynaecological disease. hydroxypropylmethylcellulose-lactose matrix 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 12165085-11 2002 These data indicate that (1) T-HPMC lines mimic the morphological and functional features of P-HPMC, (2) P-HPMC and T-HPMC constituitively produce IL-6 and IL-8, which is enhanced by hIL-1beta and hTNF-alpha and (3) HPMC in vivo may participate in the pathogenesis of benign and malignant gynaecological disease. t-hpmc 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 12165085-11 2002 These data indicate that (1) T-HPMC lines mimic the morphological and functional features of P-HPMC, (2) P-HPMC and T-HPMC constituitively produce IL-6 and IL-8, which is enhanced by hIL-1beta and hTNF-alpha and (3) HPMC in vivo may participate in the pathogenesis of benign and malignant gynaecological disease. hydroxypropylmethylcellulose-lactose matrix 95-99 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 12165097-4 2002 Incubation of FLS with a synthetic PPARgamma ligand, troglitazone, inhibited endogenous production of TNF-alpha, IL-6 and IL-8, as well as matrix metalloprotease-3 (MMP-3), without inducing apoptosis of the cells. Troglitazone 53-65 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 12088610-5 2002 Additionally, P. acnes-induced IL-8 secretion was inhibited by roxithromycin, a macrolide antibiotic, and its inhibitory effect seemed to be partially associated with the inhibition of P. acnes-induced NF-kappaB activation. Roxithromycin 63-76 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 12088610-5 2002 Additionally, P. acnes-induced IL-8 secretion was inhibited by roxithromycin, a macrolide antibiotic, and its inhibitory effect seemed to be partially associated with the inhibition of P. acnes-induced NF-kappaB activation. Macrolides 80-89 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 12173800-10 2002 Pulmonary TNF-alpha, IL-beta, and IL-8 concentrations were attenuated in the ceftazidime group compared with those in the placebo group (p < 0.001, p = 0.02, and p = 0.003). Ceftazidime 77-88 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 12161534-11 2002 IL-8 decreased apoptosis rate in endometrial stromal cells as evaluated by terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end-labeling assay. deoxyuridine triphosphate 122-147 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12133975-5 2002 PMA plus A23187 or IgE plus anti-IgE induced the production of IL-8 and GM-CSF in supernatants of HMC-1 cells and IL-4 and IL-6 in supernatants of KU812 cells. Calcimycin 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 12220349-6 2002 After daily fluoride release was measured for 60 days, samples were refluoridated in 1000-ppm sodium fluoride (NaF) solutions (pH 6.6) for 10 min and fluoride release was measured daily for a total of 5 days. Sodium Fluoride 94-109 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 12220349-11 2002 Sample exposures to 1000 ppm NaF solution increased the 24-h fluoride release from all fluoride-containing materials. Fluorides 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 12220349-11 2002 Sample exposures to 1000 ppm NaF solution increased the 24-h fluoride release from all fluoride-containing materials. Fluorides 87-95 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 12117995-3 2002 The inhibitor genistein decreased NF-kappaB nuclear translocation and IL-8 gene transcription in addition to acting on posttranscriptional processing. Genistein 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 12107097-3 2002 The human melanoma cells A375SM (high IL-8 producer) and TXM-13 (intermediate IL-8 producer) were injected subcutaneously into nude mice, which were then treated with ABX-IL8 (1 mg/3 times weekly, i.p., for 3 weeks). CHEMBL369125 167-170 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 11986301-8 2002 sTLR2 partially attenuated the iPGN-induced NF-kappaB activation in TLR2-transfected HEK 293 cells and the iPGN-induced IL-8 secretion in U937 cells. ipgn 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 12115542-11 2002 Finally, RA decreased the ability of tumor-activated macrophages to secrete IL-8 and VEGF. Tretinoin 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 11978798-0 2002 A novel pathway for nickel-induced interleukin-8 expression. Nickel 20-26 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 11978798-3 2002 Therefore, cell culture experiments with BEAS-2B human airway epithelial cells were conducted to test the hypothesis that exposure to non-cytotoxic levels of Ni3S2 induces expression of inflammatory cytokines such as interleukin-8 (IL-8). ni3s2 158-163 C-X-C motif chemokine ligand 8 Homo sapiens 217-230 11978798-3 2002 Therefore, cell culture experiments with BEAS-2B human airway epithelial cells were conducted to test the hypothesis that exposure to non-cytotoxic levels of Ni3S2 induces expression of inflammatory cytokines such as interleukin-8 (IL-8). ni3s2 158-163 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 11978798-4 2002 Exposure to Ni3S2 for 48 h was required to significantly increase IL-8 protein levels. ni3s2 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 11978798-7 2002 Transfection with truncated IL-8 promoter constructs linked to the luciferase gene demonstrated that nickel-induced IL-8 transcription required -272 bp of the promoter relative to the transcriptional start site. Nickel 101-107 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 11978798-7 2002 Transfection with truncated IL-8 promoter constructs linked to the luciferase gene demonstrated that nickel-induced IL-8 transcription required -272 bp of the promoter relative to the transcriptional start site. Nickel 101-107 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 11978798-9 2002 Transfection with a dominant negative AP-1 construct or mutation of the AP-1, GATA, or C/EBP sites in the -272-bp IL-8 promoter construct blocked induction by nickel. gata 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 11978798-9 2002 Transfection with a dominant negative AP-1 construct or mutation of the AP-1, GATA, or C/EBP sites in the -272-bp IL-8 promoter construct blocked induction by nickel. Nickel 159-165 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 11978798-10 2002 Inhibiting ERK, phosphatidylinositol 3-kinase, but not p38 kinase, diacylglycerol kinase, or hypoxia-inducible factor-1alpha, attenuated nickel induction of IL-8. Nickel 137-143 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 11978798-11 2002 These studies indicate that nickel induced IL-8 transcription through a novel pathway that requires both AP-1 and non-traditional transcription factors. Nickel 28-34 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 12060565-4 2002 1) Bleomycin-treated THP-1 cells increased tumor necrosis factor (TNF)-alpha, interleukin (IL)-8, and IL-1beta production in dose- and time-dependent patterns, as we have observed with SP-A. Bleomycin 3-12 C-X-C motif chemokine ligand 8 Homo sapiens 78-96 12091253-6 2002 The blockade of p38 with the pharmacologic inhibitor SB203580 abrogated IL-8 production by cell stretching, and an inhibitor of the p44/42 pathway, PD98059, partially inhibited the IL-8 response. SB 203580 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 12091250-2 2002 As cigarette smoke (CS) and epidermal growth factor (EGF) both cause release of interleukin-8 (IL-8) from epithelial cells in vitro, we investigated whether autocrine ligands for the EGF receptor (EGFR) are involved in this proinflammatory response to CS. Cesium 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 80-93 12091253-6 2002 The blockade of p38 with the pharmacologic inhibitor SB203580 abrogated IL-8 production by cell stretching, and an inhibitor of the p44/42 pathway, PD98059, partially inhibited the IL-8 response. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 148-155 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 12091250-2 2002 As cigarette smoke (CS) and epidermal growth factor (EGF) both cause release of interleukin-8 (IL-8) from epithelial cells in vitro, we investigated whether autocrine ligands for the EGF receptor (EGFR) are involved in this proinflammatory response to CS. Cesium 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 12091250-7 2002 Furthermore, ~ 45% of CS-induced IL-8 release was inhibited by a neutralising anti-EGFR. Cesium 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 12115021-14 2002 Furosemide exhibited an anti-inflammatory effect through inhibition of production and release of cytokines interleukin (IL)-6, IL-8, and tumor necrosis factor-alpha from peripheral mononuclear cells, which may have a beneficial effect on local inflamed tissue imbalance in the ratio of different cytokines, thus improving the sensitivity of target cells to endogenous glucocorticosteroids. Furosemide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 127-164 12091253-7 2002 A nonspecific tyrosine kinase inhibitor, genistein, also blocked the stretch-induced IL-8 production. Genistein 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 12117719-6 2002 Attenuation of the C pneumoniae-induced activation of NF-kappaB by aspirin also reduced the secretion of interleukin-6 and interleukin-8, indicating efficient inhibition of NF-kappaB gene expression. Aspirin 67-74 C-X-C motif chemokine ligand 8 Homo sapiens 123-136 12126020-0 2002 Exposure to 200 ppm of methanol increases the concentrations of interleukin-1beta and interleukin-8 in nasal secretions of healthy volunteers. Methanol 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 12126020-7 2002 The median concentrations of IL-8 and IL-1beta were significantly elevated after exposure to 200 ppm of methanol as compared to exposure to 20 ppm (IL-1beta, 21.4 versus 8.3 pg/mL, p = .001; IL-8, 424 versus 356 pg/mL, p = .02). Methanol 104-112 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 12126020-7 2002 The median concentrations of IL-8 and IL-1beta were significantly elevated after exposure to 200 ppm of methanol as compared to exposure to 20 ppm (IL-1beta, 21.4 versus 8.3 pg/mL, p = .001; IL-8, 424 versus 356 pg/mL, p = .02). Methanol 104-112 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 12126020-9 2002 Both IL-8 and IL-1beta proved to be sensitive indicators for subclinical irritating effects of methanol in vivo. Methanol 95-103 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 12117737-0 2002 Simvastatin reduces expression of cytokines interleukin-6, interleukin-8, and monocyte chemoattractant protein-1 in circulating monocytes from hypercholesterolemic patients. Simvastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 12161102-0 2002 Green tea polyphenol blocks h(2)o(2)-induced interleukin-8 production from human alveolar epithelial cells. Polyphenols 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 12117737-4 2002 METHODS AND RESULTS: In this study, we asked whether simvastatin can influence in vitro and in vivo production of the proinflammatory cytokines interleukin (IL)-6, IL-8, and monocyte chemoattractant protein-1. Simvastatin 53-64 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 12117737-7 2002 Furthermore, simvastatin decreased the expression of IL-6, IL-8, and monocyte chemoattractant protein-1 mRNA in peripheral blood mononuclear cells. Simvastatin 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 12199625-0 2002 The effect of high molecular weight dextran sulfate on the production of interleukin-8 in monocyte cell culture. Dextran Sulfate 36-51 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 12199625-5 2002 We hereby postulate that HMDS induces IL-8 biosynthesis in monocyte cell culture. hexamethylsilazane 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 12117643-4 2002 Independently, RV16, NO2, and O3 rapidly increased release of the inflammatory cytokine interleukin-8 through oxidant-dependent mechanisms. Nitrogen Dioxide 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 12070216-4 2002 This increase in PKC is observed with 15 min of HDE treatment, and kinase activity reaches peak activity by 1-2 h of HDE treatment before returning to baseline PKC levels between 6 and 24 h. The classic PKC inhibitor, calphostin C, blocks HDE-stimulated PKC activity and associated IL-8 and IL-6 release. calphostin C 218-230 C-X-C motif chemokine ligand 8 Homo sapiens 282-286 12100898-6 2002 RESULTS: Significantly elevated percentages of BAL neutrophils and IL-8 levels were found at the pre-clinical stage of BOS, on average 151 +/- 164 days and 307 +/- 266 days, respectively, before diagnosis of BOS. N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 12056817-2 2002 We found a high level of IL-8 production in SK-N-MC human primitive neuroectodermal tumor cells transfected with the human RET gene (SK-N-MC (RET) cells) in response to glial cell line-derived neurotrophic factor (GDNF) stimulation. sk-n-mc 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 12056817-2 2002 We found a high level of IL-8 production in SK-N-MC human primitive neuroectodermal tumor cells transfected with the human RET gene (SK-N-MC (RET) cells) in response to glial cell line-derived neurotrophic factor (GDNF) stimulation. sk-n-mc 133-140 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 12056817-5 2002 The results showed that a MEK1 inhibitor, PD98059, a p38MAPK inhibitor, SB202190, and a protein kinase C (PKC) inhibitor, Calphostin C, markedly decreased the IL-8 secretion from SK-N-MC (RET) cells at 24 h after GDNF stimulation. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 42-49 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 12056817-5 2002 The results showed that a MEK1 inhibitor, PD98059, a p38MAPK inhibitor, SB202190, and a protein kinase C (PKC) inhibitor, Calphostin C, markedly decreased the IL-8 secretion from SK-N-MC (RET) cells at 24 h after GDNF stimulation. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 12056817-5 2002 The results showed that a MEK1 inhibitor, PD98059, a p38MAPK inhibitor, SB202190, and a protein kinase C (PKC) inhibitor, Calphostin C, markedly decreased the IL-8 secretion from SK-N-MC (RET) cells at 24 h after GDNF stimulation. calphostin C 122-134 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 12056817-5 2002 The results showed that a MEK1 inhibitor, PD98059, a p38MAPK inhibitor, SB202190, and a protein kinase C (PKC) inhibitor, Calphostin C, markedly decreased the IL-8 secretion from SK-N-MC (RET) cells at 24 h after GDNF stimulation. sk-n-mc 179-186 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 12115500-9 2002 Here, we report on a new autocrine function of secreted interleukin-8 and the intracellular signal transduction leading to the regulation of cytosolic calcium and to a migratory tumor cell phenotype. Calcium 151-158 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 12100025-0 2002 Anti-CD45 isoform antibodies enhance phagocytosis and gene expression of IL-8 and TNF-alpha in human neutrophils by differential suppression on protein tyrosine phosphorylation and p56lck tyrosine kinase. Tyrosine 152-160 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 12087060-7 2002 In the in vitro study, a cooperative suppressive effect of NE (10(-6) M to 10(-8) M) and cortisol (10(-6) M and 10(-7) M) on secretion of IL-8 and TNF from primary early culture mixed RA synoviocytes was observed. Hydrocortisone 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 12060853-4 2002 Incubation with hypericin, a natural photosensitizer increased IL-8 significantly but only in HK1 cells. hypericin 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 12060853-7 2002 It is interesting that PDT which is known to upregulate IL-8 transcription via reactive oxygen species and activate the IL-10 promoter did not alter IL-8 levels in either of the NPC cell lines nor induced the production of IL-10. Reactive Oxygen Species 79-102 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 12161102-0 2002 Green tea polyphenol blocks h(2)o(2)-induced interleukin-8 production from human alveolar epithelial cells. Hydrogen Peroxide 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 12161102-2 2002 Reactive oxygen species may stimulate the production of neutrophil chemotactic factors such as interleukin-8 (IL-8), from alveolar epithelial cells, causing recruitment and activation of neutrophils in the reperfused tissue. Reactive Oxygen Species 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 12161102-2 2002 Reactive oxygen species may stimulate the production of neutrophil chemotactic factors such as interleukin-8 (IL-8), from alveolar epithelial cells, causing recruitment and activation of neutrophils in the reperfused tissue. Reactive Oxygen Species 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 12161102-4 2002 In the present study, we found that green tea polyphenol significantly inhibited IL-8 production induced by hydrogen peroxide (H(2)O(2)) in human lung alveolar epithelial cells (A549 line). Polyphenols 46-56 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 12161102-4 2002 In the present study, we found that green tea polyphenol significantly inhibited IL-8 production induced by hydrogen peroxide (H(2)O(2)) in human lung alveolar epithelial cells (A549 line). Hydrogen Peroxide 108-125 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 12161102-7 2002 We speculate that green tea polyphenol may inhibit H(2)O(2)-induced IL-8 production from A549 cells through inactivation of JNK and p38. Polyphenols 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 12161102-7 2002 We speculate that green tea polyphenol may inhibit H(2)O(2)-induced IL-8 production from A549 cells through inactivation of JNK and p38. Hydrogen Peroxide 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 12469754-0 2002 Effect of application time of APF and NaF gels on microhardness and fluoride uptake of in vitro enamel caries. Fluorides 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 11997318-6 2002 Furthermore, an antisense oligodeoxyribonucleotide targeted against TRAF6 mRNA blunted p38 and SAPK/JNK but not ERK1/2 MAPK activities, as well as IL-8 and MCP-1 production, arguing that TRAF6 is an upstream activator. Oligodeoxyribonucleotides 26-50 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 12045128-7 2002 Nanomolar concentrations of LXA4 and LXB4 inhibited the IL-8 released by peripheral blood mononuclear cells from the two groups of patients with asthma: a maximal inhibition of 29.4% (p < 0.01) was observed for patients with mild asthma, and 41.5% inhibition (p < 0.001) for patients with severe asthma at 1 nM and 100 nM LXA4 concentrations, respectively. lipoxin A4 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 12011031-2 2002 Consequently, gingipains-R reduced lipopolysaccharide-induced interleukin-8 production by HGF, indicating that gingipains-R inhibited CD14-dependent HGF activation and are involved in immune evasion by the bacterium in periodontal tissues. gingipains-r reduced lipopolysaccharide 14-53 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 12045128-7 2002 Nanomolar concentrations of LXA4 and LXB4 inhibited the IL-8 released by peripheral blood mononuclear cells from the two groups of patients with asthma: a maximal inhibition of 29.4% (p < 0.01) was observed for patients with mild asthma, and 41.5% inhibition (p < 0.001) for patients with severe asthma at 1 nM and 100 nM LXA4 concentrations, respectively. lipoxin B4 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 12079131-0 2002 Human vascular endothelial cells express pattern recognition receptors for fungal glucans which stimulates nuclear factor kappaB activation and interleukin 8 production. Glucans 82-89 C-X-C motif chemokine ligand 8 Homo sapiens 144-157 12079131-8 2002 Glucan (1 microg/mL) stimulated VEC nuclear factor kappaB nuclear binding activity and Interleukin 8 expression--but not that of vascular endothelial growth factor--in a time-dependent manner. Glucans 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 87-100 12166720-2 2002 The purpose of this study was to evaluate the cytotoxic effects of sodium fluoride (NaF) on three different cell lines and the antibacterial potency on Streptococcus sobrinus. Sodium Fluoride 67-82 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 12132790-13 2002 This is against the hypothesis that nicotine exerts a direct pro-inflammatory action via interleukin-1beta and interleukin-8. Nicotine 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 11992543-8 2002 MEK inhibitor U0126 preferentially blocked AP-1 activity and expression of both IL-8 and VEGF, while PI3K inhibitor LY-294002 or a dominant negative inhibitor-kappaB preferentially blocked NF-kappaB activation and expression of IL-8 but not VEGF. U 0126 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 11920660-4 2002 The results showed that fucan, dextran derivatives, and heparin differentially (1) triggered interleukin-1alpha, tumor necrosis factor alpha, interleukin-6, and interleukin-8 production by monocytes in a dose-dependent manner, (2) modulated cytokine production by LPS-stimulated monocytes, and (3) specifically inhibited the binding of biotinylated LPS to monocyte membranes. fucan 24-29 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 11920660-4 2002 The results showed that fucan, dextran derivatives, and heparin differentially (1) triggered interleukin-1alpha, tumor necrosis factor alpha, interleukin-6, and interleukin-8 production by monocytes in a dose-dependent manner, (2) modulated cytokine production by LPS-stimulated monocytes, and (3) specifically inhibited the binding of biotinylated LPS to monocyte membranes. Dextrans 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 11920660-4 2002 The results showed that fucan, dextran derivatives, and heparin differentially (1) triggered interleukin-1alpha, tumor necrosis factor alpha, interleukin-6, and interleukin-8 production by monocytes in a dose-dependent manner, (2) modulated cytokine production by LPS-stimulated monocytes, and (3) specifically inhibited the binding of biotinylated LPS to monocyte membranes. Heparin 56-63 C-X-C motif chemokine ligand 8 Homo sapiens 161-174 12011031-2 2002 Consequently, gingipains-R reduced lipopolysaccharide-induced interleukin-8 production by HGF, indicating that gingipains-R inhibited CD14-dependent HGF activation and are involved in immune evasion by the bacterium in periodontal tissues. gingipains-r 14-26 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 12051749-2 2002 In this report we employed CXCL8((3-73))K11R as a template to generate CXCL8/IL-8 analogues with antagonist activities, using site-directed mutagenesis to introduce conservative amino acid substitutions into the first turn within the molecule"s beta-pleated sheet region (G31P, P32G) and, in association with these, into the putative receptor-recognition site (T12S, H13F, F17S). k11r 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 12023021-4 2002 By prednisolone or phorbol myristate acetate treatment, EC-SOD levels were correlated negatively with levels of IL-6 and IL-8. Prednisolone 3-15 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 12023021-4 2002 By prednisolone or phorbol myristate acetate treatment, EC-SOD levels were correlated negatively with levels of IL-6 and IL-8. Tetradecanoylphorbol Acetate 19-44 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 12166728-1 2002 A new route has been devised, leading to the production of phosphorus thiotrihalides, SPX3 where X = F, Br and I by an on-line process using phosphorus thiotrichloride, SPCl3 as starting compound gassed over the following heated salts NaF, KBr and KI at 530, 800 and 440 degrees C, respectively. phosphorus thiotrihalides 59-84 C-X-C motif chemokine ligand 8 Homo sapiens 235-238 12126643-8 2002 SB203580, a specific P38 MAPK inhibitor, partially blocked IL-1beta induction of IL-8 mRNA, IL-8 promoter activity, and AP-1 nuclear extract binding but not NF-kappaB DNA binding. SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 12126643-8 2002 SB203580, a specific P38 MAPK inhibitor, partially blocked IL-1beta induction of IL-8 mRNA, IL-8 promoter activity, and AP-1 nuclear extract binding but not NF-kappaB DNA binding. SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 12016098-5 2002 Induced sputum inflammatory cells, neutrophils, interleukin-8, myeloperoxidase, and lactoferrin were all significantly reduced by about 22% by theophylline. Theophylline 143-155 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 12016098-6 2002 Neutrophils from subjects treated with theophylline showed reduced chemotaxis to N-formyl-met-leu-phe (approximately 28%) and interleukin-8 (approximately 60%). Theophylline 39-51 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 12051749-2 2002 In this report we employed CXCL8((3-73))K11R as a template to generate CXCL8/IL-8 analogues with antagonist activities, using site-directed mutagenesis to introduce conservative amino acid substitutions into the first turn within the molecule"s beta-pleated sheet region (G31P, P32G) and, in association with these, into the putative receptor-recognition site (T12S, H13F, F17S). k11r 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 12051749-2 2002 In this report we employed CXCL8((3-73))K11R as a template to generate CXCL8/IL-8 analogues with antagonist activities, using site-directed mutagenesis to introduce conservative amino acid substitutions into the first turn within the molecule"s beta-pleated sheet region (G31P, P32G) and, in association with these, into the putative receptor-recognition site (T12S, H13F, F17S). k11r 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 27-32 12010777-0 2002 Caprylic acid and medium-chain triglycerides inhibit IL-8 gene transcription in Caco-2 cells: comparison with the potent histone deacetylase inhibitor trichostatin A. octanoic acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 11891214-6 2002 Selective MAP kinase kinase (MEK)1/2 inhibitors, PD98059 and U0126, inhibited, in a dose-dependent manner, ML-1-induced expression of IL-6 and IL-8. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 11891214-6 2002 Selective MAP kinase kinase (MEK)1/2 inhibitors, PD98059 and U0126, inhibited, in a dose-dependent manner, ML-1-induced expression of IL-6 and IL-8. U 0126 61-66 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 12051749-3 2002 We then examined their impact on the analogues" biological activities and found that a G31P substitution rendered CXCL8((3-73))K11R a high affinity antagonist of CXCL8/IL-8. k11r 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 114-119 12051749-3 2002 We then examined their impact on the analogues" biological activities and found that a G31P substitution rendered CXCL8((3-73))K11R a high affinity antagonist of CXCL8/IL-8. k11r 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 162-167 12051749-3 2002 We then examined their impact on the analogues" biological activities and found that a G31P substitution rendered CXCL8((3-73))K11R a high affinity antagonist of CXCL8/IL-8. k11r 127-131 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 12062638-12 2002 Finally, generation of reactive oxygen species (which occurs during alcohol metabolism) and products of lipid peroxidation induce production of cytokines, such as TNF and IL-8. Reactive Oxygen Species 23-46 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 12062638-12 2002 Finally, generation of reactive oxygen species (which occurs during alcohol metabolism) and products of lipid peroxidation induce production of cytokines, such as TNF and IL-8. Alcohols 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 11996908-1 2002 The fluoroaluminate (AlF(4)(-)) ion and sodium fluoride (NaF) have previously been shown to be bone cell mitogens. Sodium Fluoride 40-55 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 11996908-5 2002 NaF, AlF(3), and AlF(4)(-), each at 50-100 micromol/L, increased [3H]thymidine incorporation in TE85 cells. Tritium 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 11996908-5 2002 NaF, AlF(3), and AlF(4)(-), each at 50-100 micromol/L, increased [3H]thymidine incorporation in TE85 cells. Thymidine 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 12010777-0 2002 Caprylic acid and medium-chain triglycerides inhibit IL-8 gene transcription in Caco-2 cells: comparison with the potent histone deacetylase inhibitor trichostatin A. Triglycerides 31-44 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 12010777-4 2002 In this study we examined whether caprylic acid, one of the MCFAs, and MCT suppress IL-8 secretion by differentiated Caco-2 cells. octanoic acid 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 12010777-6 2002 We found for the first time that caprylic acid and MCT suppress IL-8 secretion by Caco-2 cells at the transcriptional level when precultured together for 24 h. We also tried to clarify the mechanism of IL-8 gene inhibition by examining the activation of NF-kappaB and other transcription factors by electrophoretic mobility shift assay (EMSA), and found that caprylic acid did not modulate their activation. octanoic acid 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 12010777-6 2002 We found for the first time that caprylic acid and MCT suppress IL-8 secretion by Caco-2 cells at the transcriptional level when precultured together for 24 h. We also tried to clarify the mechanism of IL-8 gene inhibition by examining the activation of NF-kappaB and other transcription factors by electrophoretic mobility shift assay (EMSA), and found that caprylic acid did not modulate their activation. octanoic acid 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 12010777-8 2002 The result of dual-luciferase assay using Caco-2 cells transfected with IL-8 promoter/luciferase reporter plasmid revealed that caprylic acid inhibited the activation of IL-8 promoter. octanoic acid 128-141 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 12010777-8 2002 The result of dual-luciferase assay using Caco-2 cells transfected with IL-8 promoter/luciferase reporter plasmid revealed that caprylic acid inhibited the activation of IL-8 promoter. octanoic acid 128-141 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 12010777-13 2002 TSA rapidly induced H4 acetylation in IL-8 promoter chromatin, whereas caprylic acid did not. trichostatin A 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 12010777-14 2002 These results suggest that the inhibition of IL-8 gene transcription induced by caprylic acid and TSA does not necessarily require the marked suppression of transcription factors, and the mechanism of inhibition of IL-8 gene transcription may be different between caprylic acid and TSA. octanoic acid 80-93 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 12010777-14 2002 These results suggest that the inhibition of IL-8 gene transcription induced by caprylic acid and TSA does not necessarily require the marked suppression of transcription factors, and the mechanism of inhibition of IL-8 gene transcription may be different between caprylic acid and TSA. trichostatin A 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 12010777-14 2002 These results suggest that the inhibition of IL-8 gene transcription induced by caprylic acid and TSA does not necessarily require the marked suppression of transcription factors, and the mechanism of inhibition of IL-8 gene transcription may be different between caprylic acid and TSA. octanoic acid 264-277 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 12010777-14 2002 These results suggest that the inhibition of IL-8 gene transcription induced by caprylic acid and TSA does not necessarily require the marked suppression of transcription factors, and the mechanism of inhibition of IL-8 gene transcription may be different between caprylic acid and TSA. octanoic acid 264-277 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 12010777-14 2002 These results suggest that the inhibition of IL-8 gene transcription induced by caprylic acid and TSA does not necessarily require the marked suppression of transcription factors, and the mechanism of inhibition of IL-8 gene transcription may be different between caprylic acid and TSA. trichostatin A 282-285 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 11953364-7 2002 Pretreatment of cells with the highly specific MEK1/2 inhibitor U0126, the p38 inhibitor SB203580, and/or the proteasome inhibitor ALLN led to inhibition of the IL-8 secretion induced in EHEC-infected T84 cells. U 0126 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 11953364-7 2002 Pretreatment of cells with the highly specific MEK1/2 inhibitor U0126, the p38 inhibitor SB203580, and/or the proteasome inhibitor ALLN led to inhibition of the IL-8 secretion induced in EHEC-infected T84 cells. SB 203580 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 11953371-7 2002 IL-8 slightly stimulated butyric acid- or Fas-induced Jurkat-cell apoptosis in a dose-dependent manner, although a low dose of IL-8 had a mildly inhibitory effect on apoptosis. Butyric Acid 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11953371-7 2002 IL-8 slightly stimulated butyric acid- or Fas-induced Jurkat-cell apoptosis in a dose-dependent manner, although a low dose of IL-8 had a mildly inhibitory effect on apoptosis. ammonium ferrous sulfate 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12003967-0 2002 Clarithromycin suppresses lipopolysaccharide-induced interleukin-8 production by human monocytes through AP-1 and NF-kappa B transcription factors. Clarithromycin 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 53-66 12003967-6 2002 A luciferase reporter gene assay with plasmids containing a serially deleted IL-8 promoter fragment showed that both the activator protein-1 (AP-1) and/or the nuclear factor-kappa B (NF-kapp aB) binding sequences were responsible for the LPS and clarithromycin responsiveness of the IL-8 promoter. Clarithromycin 246-260 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 12003967-9 2002 Our results indicate that clarithromycin modified inflammation by sup-pressing IL-8 production and that clarithromycin may affect the expression of other genes through AP-1 and NF-kappa B. Clarithromycin 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 12015158-5 2002 Furthermore, berry polyphenols also reduced TNFalpha induced up-regulation of various inflammatory mediators (IL-8, MCP-1 and ICAM-1) involved in the recruitment of leukocytes to sites of damage or inflammation along the endothelium. Polyphenols 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 11971003-4 2002 IL-8-stimulated neutrophil adhesion to fibrinogen was blocked 50% by the MAPK/extracellular signal-related kinase-activating enzyme inhibitor PD098059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 142-150 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11971003-5 2002 Adhesion was blocked approximately 75% by inhibition of the phosphatidylinositol-3 kinase (PI3K) pathway with LY294002, supporting that activation of both MAPK and PI3K may play a role in IL-8-dependent inside-out signals that activate Mac-1. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 110-118 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 11971003-6 2002 Activation of MAPK was inhibited in IL-8-stimulated cells in the presence of PI3K inhibitors LY294002 or wortmannin, supporting a model in which PI3K is upstream of MAPK. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 11971003-6 2002 Activation of MAPK was inhibited in IL-8-stimulated cells in the presence of PI3K inhibitors LY294002 or wortmannin, supporting a model in which PI3K is upstream of MAPK. Wortmannin 105-115 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 11971003-7 2002 IL-8-stimulated neutrophil adhesion was inhibited 50% by bisindolylmaleimide-I, implicating protein kinase C (PKC) in the intracellular signaling from the IL-8R to Mac-1. bisindolylmaleimide I 57-78 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12038622-0 2002 Titanium particles induce the immediate early stress responsive chemokines IL-8 and MCP-1 in osteoblasts. Titanium 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 12038622-3 2002 In this study, we now demonstrate that Ti particles can rapidly induce the chemotactic cytokines interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1), two immediate early stress responsive chemokines important for the activation and chemotaxis of neutrophils and macrophages, respectively. Titanium 39-41 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 12038622-3 2002 In this study, we now demonstrate that Ti particles can rapidly induce the chemotactic cytokines interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1), two immediate early stress responsive chemokines important for the activation and chemotaxis of neutrophils and macrophages, respectively. Titanium 39-41 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 12038622-6 2002 Actinomycin D, a potent RNA polymerase II inhibitor, blocked the Ti particle induction of IL-8 and MCP-1 mRNA expression, whereas cycloheximide, which inhibits protein synthesis, failed to inhibit chemokine gene expression suggesting Ti particles directly target activation of chemokine gene transcription. Dactinomycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 12038622-8 2002 Taken together, these data demonstrate that Ti particles can activate transcription of the stress responsive chemokine genes IL-8 and MCP-1 in human osteoblasts. Titanium 44-46 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 12162465-7 2002 In airway epithelial cells, sphingosine-1-phosphate and PA-induced IL-8 secretion and ERKI/2 phosphorylation is regulated by PA. sphingosine 1-phosphate 28-51 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 12197272-8 2002 DISCUSSION: The decrease in IL-8 serum levels observed in exposed workers might suggest an immunosuppressive effect of occupational exposure to very low doses of inorganic mercury. Mercury 172-179 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 12162440-11 2002 This study shows that the oxidant H2O2 and the pro-inflammatory mediator, TNF-a induce histone acetylation which is associated with decreased GSH levels and increased AP-1 and NF-kappaB activation leading to enhanced proinflammatory IL-8 release in alveolar epithelial cells. Hydrogen Peroxide 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 12162440-10 2002 Both H2O2 and TNF-alpha significantly increased IL-8 release, which was further enhanced by pre-treatment of A549 cells with TSA compared to the individual treatments. Hydrogen Peroxide 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 12162465-7 2002 In airway epithelial cells, sphingosine-1-phosphate and PA-induced IL-8 secretion and ERKI/2 phosphorylation is regulated by PA. Phosphatidic Acids 56-58 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 12162440-10 2002 Both H2O2 and TNF-alpha significantly increased IL-8 release, which was further enhanced by pre-treatment of A549 cells with TSA compared to the individual treatments. trichostatin A 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 12162440-11 2002 This study shows that the oxidant H2O2 and the pro-inflammatory mediator, TNF-a induce histone acetylation which is associated with decreased GSH levels and increased AP-1 and NF-kappaB activation leading to enhanced proinflammatory IL-8 release in alveolar epithelial cells. Glutathione 142-145 C-X-C motif chemokine ligand 8 Homo sapiens 233-237 12162465-7 2002 In airway epithelial cells, sphingosine-1-phosphate and PA-induced IL-8 secretion and ERKI/2 phosphorylation is regulated by PA. Phosphatidic Acids 125-127 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 11897597-1 2002 A 14-member macrolide was found to inhibit interleukin-8 (IL-8) synthesis in lipopolysaccharide-stimulated neutrophils but did not accelerate apoptosis in activated neutrophils. -member macrolide 4-21 C-X-C motif chemokine ligand 8 Homo sapiens 43-56 12096924-0 2002 Glutamine decreases interleukin-8 and interleukin-6 but not nitric oxide and prostaglandins e(2) production by human gut in-vitro. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 20-33 12096924-8 2002 RESULTS: Glutamine decreased IL-8 and IL-6 in-vitro production: 63 [2-173] vs 100 [19-177] and 37 [5-489] vs 100 [33-431], both P<0.05. Glutamine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 12096924-9 2002 IL-8 mRNA level also decreased in biopsies cultured with 5 mM glutamine: 26 [13-142] vs 92 [34-215], P<0.05. Glutamine 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11943329-4 2002 Both hr IL-8 and the culture supernatant from PBMC treated with EWD yielded a distinct band, molecular weight of 6-8kDa, in sodium-dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) with 15% loading gel. Sodium Dodecyl Sulfate 124-146 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 11943329-4 2002 Both hr IL-8 and the culture supernatant from PBMC treated with EWD yielded a distinct band, molecular weight of 6-8kDa, in sodium-dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) with 15% loading gel. polyacrylamide 147-161 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 11943329-4 2002 Both hr IL-8 and the culture supernatant from PBMC treated with EWD yielded a distinct band, molecular weight of 6-8kDa, in sodium-dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) with 15% loading gel. Sodium Dodecyl Sulfate 183-186 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 11943329-9 2002 A single protein band with 6-8kDa was shown in both the eluate and hr IL-8 when analyzed by SDS-PAGE and Western blotting using anti-hr IL-8 pAb, suggesting that the chemotactic factor for feline PMN is IL-8, 6-8kDa, produced by PBMC treated with EWD. Sodium Dodecyl Sulfate 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 11943329-11 2002 The eluate under these conditions also showed a distinct band in molecular weight of 6-8kDa in SDS-PAGE and Western blotting and was very active in chemotactic activity of PMN.IL-8 mRNA gene expression on feline PBMC was analyzed by reverse transcriptase-polymerase chain reaction (RT-PCR) assay using a series of oligonucleotides, each 22 mer, derived from feline IL-8. Sodium Dodecyl Sulfate 95-98 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 11897597-1 2002 A 14-member macrolide was found to inhibit interleukin-8 (IL-8) synthesis in lipopolysaccharide-stimulated neutrophils but did not accelerate apoptosis in activated neutrophils. -member macrolide 4-21 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 11950713-6 2002 (2) During folic acid treatment, normalization of homocysteine levels was accompanied by a marked reduction in oxidized low density lipoprotein-stimulated release of CXC chemokines (ie, GROalpha, ENA-78, and interleukin-8) and CC chemokines (ie, monocyte chemoattractant peptide-1 and RANTES) in peripheral blood mononuclear cells from these individuals. Folic Acid 11-21 C-X-C motif chemokine ligand 8 Homo sapiens 208-221 12034025-0 2002 Regulation of constitutive and induced NF-kappaB activation in malignant melanoma cells by capsaicin modulates interleukin-8 production and cell proliferation. Capsaicin 91-100 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 11950713-6 2002 (2) During folic acid treatment, normalization of homocysteine levels was accompanied by a marked reduction in oxidized low density lipoprotein-stimulated release of CXC chemokines (ie, GROalpha, ENA-78, and interleukin-8) and CC chemokines (ie, monocyte chemoattractant peptide-1 and RANTES) in peripheral blood mononuclear cells from these individuals. Homocysteine 50-62 C-X-C motif chemokine ligand 8 Homo sapiens 208-221 11895948-5 2002 Lactoferrin strongly inhibited the interaction of radiolabeled IL-8 to immobilized heparin, whereas a lactoferrin variant lacking the amino acid residues essential for heparin binding was not inhibitory. Heparin 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 11927646-0 2002 Ambient pCO2 modulates intracellular pH, intracellular oxidant generation, and interleukin-8 secretion in human neutrophils. pco2 8-12 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 11927646-4 2002 Further, hypo- and hypercarbia increase and decrease, respectively, the release of IL-8 from LPS-stimulated cells; both effects are attenuated by the carbonic anhydrase inhibitor, acetazolamide. Acetazolamide 180-193 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 11910356-0 2002 Clostridium difficile toxin A triggers human colonocyte IL-8 release via mitochondrial oxygen radical generation. Reactive Oxygen Species 87-101 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 11910356-3 2002 METHODS: NF-kappaB activation and IL-8 release in response to toxin A were correlated with reactive oxygen intermediate (ROI) generation and ATP production in HT-29 monolayers or HT-29 cells exposed to ethidium bromide (EB) to inhibit mitochondrial function. reactive oxygen intermediate 91-119 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 11910356-3 2002 METHODS: NF-kappaB activation and IL-8 release in response to toxin A were correlated with reactive oxygen intermediate (ROI) generation and ATP production in HT-29 monolayers or HT-29 cells exposed to ethidium bromide (EB) to inhibit mitochondrial function. ROI 121-124 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 11910356-3 2002 METHODS: NF-kappaB activation and IL-8 release in response to toxin A were correlated with reactive oxygen intermediate (ROI) generation and ATP production in HT-29 monolayers or HT-29 cells exposed to ethidium bromide (EB) to inhibit mitochondrial function. Ethidium 202-218 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 11989791-5 2002 We demonstrate that blockade of the p42/p44 MAPK signaling pathway by the inhibitor PD98059 suppresses IL-8-mediated PMNL chemotaxis. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 84-91 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 11907118-6 2002 A monomeric form of IL-8, N-methyl-leucine 25 IL-8, was not retained as long in lungs as recombinant human IL-8, indicating that dimerization of IL-8 is a mechanism that increases the local concentration and prolongs the retention of (125)I-labeled IL-8 in lungs. n-methyl-leucine 26-42 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 12034025-6 2002 Further, downregulation of IL-8 expression in capsaicin-treated melanoma cells resulted in inhibition of in vitro cell proliferation. Capsaicin 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 12034025-2 2002 Addition of capsaicin (8-methyl-N-vanillyl-6-nonenamide), a known inhibitor of NF-kappaB, resulted in the inhibition of constitutive as well as IL-1beta-induced and TNF-alpha-induced IL-8 expression in melanoma cells. Capsaicin 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 12034025-2 2002 Addition of capsaicin (8-methyl-N-vanillyl-6-nonenamide), a known inhibitor of NF-kappaB, resulted in the inhibition of constitutive as well as IL-1beta-induced and TNF-alpha-induced IL-8 expression in melanoma cells. Capsaicin 23-55 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 12034025-3 2002 The inhibition of IL-8 expression was dependent on the concentration of capsaicin and duration of treatment. Capsaicin 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 12034025-5 2002 Treatment of melanoma cells with capsaicin inhibited activation of constitutive and IL-1beta-induced NF-kappaB, but not AP-1, leading to inhibition of IL-8 expression. Capsaicin 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 11912286-7 2002 The immunoreactive levels of endometrial IL-8 and MCP-1 were up-regulated by the administration of progesterone during the receptive phase of the cycle. Progesterone 99-111 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 11950021-11 2002 No NSAID showed significant effects on basal and IL-1beta stimulated IL-8 production, except CELE and IBUP, which slightly increased basal IL-8 production. Celecoxib 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 11950021-11 2002 No NSAID showed significant effects on basal and IL-1beta stimulated IL-8 production, except CELE and IBUP, which slightly increased basal IL-8 production. Ibuprofen 102-106 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 11950021-8 2002 A large amount (43%) of the IL-8 produced was stored in the alginate beads, whereas almost all IL-6 production (94%) was released in the culture supernatant. Alginates 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 11884459-7 2002 Suppression of IL-8/CXCL8 was abrogated in the presence of anti-CCR3 mAb, pertussis toxin, and wortmannin, indicating it was mediated by the CCR3 receptor, G(i) proteins, and phosphatidylinositol 3-kinase signaling. Wortmannin 95-105 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 11909816-5 2002 The nonselective adenosine agonist 5"-N-ethylcarboxamidoadenosine (NECA) increased expression of interleukin-8 (IL-8), basic fibroblast growth factor (bFGF), and vascular endothelial growth factor (VEGF) in HMEC-1, but had no effect in HUVECs. Adenosine 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 11909816-5 2002 The nonselective adenosine agonist 5"-N-ethylcarboxamidoadenosine (NECA) increased expression of interleukin-8 (IL-8), basic fibroblast growth factor (bFGF), and vascular endothelial growth factor (VEGF) in HMEC-1, but had no effect in HUVECs. Adenosine 17-26 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 11909816-5 2002 The nonselective adenosine agonist 5"-N-ethylcarboxamidoadenosine (NECA) increased expression of interleukin-8 (IL-8), basic fibroblast growth factor (bFGF), and vascular endothelial growth factor (VEGF) in HMEC-1, but had no effect in HUVECs. Adenosine-5'-(N-ethylcarboxamide) 35-65 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 11909816-5 2002 The nonselective adenosine agonist 5"-N-ethylcarboxamidoadenosine (NECA) increased expression of interleukin-8 (IL-8), basic fibroblast growth factor (bFGF), and vascular endothelial growth factor (VEGF) in HMEC-1, but had no effect in HUVECs. Adenosine-5'-(N-ethylcarboxamide) 35-65 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 11909816-5 2002 The nonselective adenosine agonist 5"-N-ethylcarboxamidoadenosine (NECA) increased expression of interleukin-8 (IL-8), basic fibroblast growth factor (bFGF), and vascular endothelial growth factor (VEGF) in HMEC-1, but had no effect in HUVECs. Adenosine-5'-(N-ethylcarboxamide) 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 11909816-5 2002 The nonselective adenosine agonist 5"-N-ethylcarboxamidoadenosine (NECA) increased expression of interleukin-8 (IL-8), basic fibroblast growth factor (bFGF), and vascular endothelial growth factor (VEGF) in HMEC-1, but had no effect in HUVECs. Adenosine-5'-(N-ethylcarboxamide) 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 11958950-0 2002 Nacystelyn inhibits oxidant-mediated interleukin-8 expression and NF-kappaB nuclear binding in alveolar epithelial cells. N-acetylcysteine lysinate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 11958950-3 2002 NAL (5 mM) enhanced intracellular glutathione (GSH) after 4 h and abolished H(2)O(2)-induced IL-8 release from A549 cells. N-acetylcysteine lysinate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 11958950-5 2002 NAL also abolished the transcriptional activation of IL-8 in an IL-8-chloramphenicol acetyl transferase (CAT) reporter system, transfected into A549 cells. N-acetylcysteine lysinate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 11958950-5 2002 NAL also abolished the transcriptional activation of IL-8 in an IL-8-chloramphenicol acetyl transferase (CAT) reporter system, transfected into A549 cells. N-acetylcysteine lysinate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 11884459-7 2002 Suppression of IL-8/CXCL8 was abrogated in the presence of anti-CCR3 mAb, pertussis toxin, and wortmannin, indicating it was mediated by the CCR3 receptor, G(i) proteins, and phosphatidylinositol 3-kinase signaling. Wortmannin 95-105 C-X-C motif chemokine ligand 8 Homo sapiens 20-25 11877327-4 2002 Pre-stimulation of cells with adenosine 5"-triphosphate (ATP) revealed a substantial Ca(2+) signalling component mediated by IL-8 (E(max)=83 +/- 8% of maximal ATP response, pEC(50) of IL-8 response=9.7 +/- 0.1). Adenosine Triphosphate 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 12027404-13 2002 In summary, while both IL-6 and IL-8 are overexpressed in paclitaxel resistant cell lines, only IL-6 has the potential to contribute directly to paclitaxel and doxorubicin resistance in U-2OS. Paclitaxel 58-68 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 11949939-11 2002 More convincingly, IL-8 antisense oligonucleotide treatment decreases IL-8 production by endometrial cells as well as cell proliferation when compared to non-sense oligonucleotide treatment. Oligonucleotides 34-49 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 11949939-11 2002 More convincingly, IL-8 antisense oligonucleotide treatment decreases IL-8 production by endometrial cells as well as cell proliferation when compared to non-sense oligonucleotide treatment. Oligonucleotides 34-49 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 11949939-11 2002 More convincingly, IL-8 antisense oligonucleotide treatment decreases IL-8 production by endometrial cells as well as cell proliferation when compared to non-sense oligonucleotide treatment. Oligonucleotides 164-179 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 11949939-12 2002 The addition of IL-8 reverses the inhibitory effect of IL-8 antisense oligonucleotides on cell proliferation. Oligonucleotides 70-86 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 11949939-12 2002 The addition of IL-8 reverses the inhibitory effect of IL-8 antisense oligonucleotides on cell proliferation. Oligonucleotides 70-86 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 11877327-4 2002 Pre-stimulation of cells with adenosine 5"-triphosphate (ATP) revealed a substantial Ca(2+) signalling component mediated by IL-8 (E(max)=83 +/- 8% of maximal ATP response, pEC(50) of IL-8 response=9.7 +/- 0.1). Adenosine Triphosphate 30-55 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 11877327-4 2002 Pre-stimulation of cells with adenosine 5"-triphosphate (ATP) revealed a substantial Ca(2+) signalling component mediated by IL-8 (E(max)=83 +/- 8% of maximal ATP response, pEC(50) of IL-8 response=9.7 +/- 0.1). Adenosine Triphosphate 30-55 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 11877327-4 2002 Pre-stimulation of cells with adenosine 5"-triphosphate (ATP) revealed a substantial Ca(2+) signalling component mediated by IL-8 (E(max)=83 +/- 8% of maximal ATP response, pEC(50) of IL-8 response=9.7 +/- 0.1). Adenosine Triphosphate 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 11756416-0 2002 Lithium induces NF-kappa B activation and interleukin-8 production in human intestinal epithelial cells. Lithium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 11756416-5 2002 This lithium-induced up-regulation of NF-kappa B and MAP kinase activation was associated with an enhancement of interleukin-8 mRNA accumulation as well as an increase in interleukin-8 protein release. Lithium 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 11756416-5 2002 This lithium-induced up-regulation of NF-kappa B and MAP kinase activation was associated with an enhancement of interleukin-8 mRNA accumulation as well as an increase in interleukin-8 protein release. Lithium 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 171-184 11906276-0 2002 Effects of coligand variation on the in vivo characteristics of Tc-99m-labeled interleukin-8 in detection of infection. Technetium 64-70 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 11906276-1 2002 In our previous studies, interleukin-8 (IL-8) was labeled with (99m)Tc using hydrazinonicotinamide (HYNIC) as bifunctional coupling agent and tricine as coligand. Technetium 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 25-38 11906276-1 2002 In our previous studies, interleukin-8 (IL-8) was labeled with (99m)Tc using hydrazinonicotinamide (HYNIC) as bifunctional coupling agent and tricine as coligand. Technetium 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 11906276-1 2002 In our previous studies, interleukin-8 (IL-8) was labeled with (99m)Tc using hydrazinonicotinamide (HYNIC) as bifunctional coupling agent and tricine as coligand. hydrazino nicotinamide 77-98 C-X-C motif chemokine ligand 8 Homo sapiens 25-38 11906276-1 2002 In our previous studies, interleukin-8 (IL-8) was labeled with (99m)Tc using hydrazinonicotinamide (HYNIC) as bifunctional coupling agent and tricine as coligand. hydrazino nicotinamide 77-98 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 11906276-1 2002 In our previous studies, interleukin-8 (IL-8) was labeled with (99m)Tc using hydrazinonicotinamide (HYNIC) as bifunctional coupling agent and tricine as coligand. tricine 142-149 C-X-C motif chemokine ligand 8 Homo sapiens 25-38 11906276-1 2002 In our previous studies, interleukin-8 (IL-8) was labeled with (99m)Tc using hydrazinonicotinamide (HYNIC) as bifunctional coupling agent and tricine as coligand. tricine 142-149 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 11906276-3 2002 In the present study, the propylaldehyde hydrazone formulation of HYNIC was introduced to stabilize HYNIC-IL-8. propylaldehyde hydrazone 26-50 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). Technetium 44-46 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). tricine 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). EDDA 90-118 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). EDDA 120-124 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). tricine 131-138 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). trisodium triphenylphosphinetrisulfonate 143-183 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). Sodium 3,3',3''-phosphinetriyltribenzenesulfonate 185-190 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). tricine 131-138 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). Niacin 209-223 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). Niacin 2-5 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). tricine 131-138 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11877327-4 2002 Pre-stimulation of cells with adenosine 5"-triphosphate (ATP) revealed a substantial Ca(2+) signalling component mediated by IL-8 (E(max)=83 +/- 8% of maximal ATP response, pEC(50) of IL-8 response=9.7 +/- 0.1). Adenosine Triphosphate 159-162 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 11906276-6 2002 HYNIC-conjugated IL-8 was labeled with (99m)Tc in the presence of either (A) tricine, (B) ethylenediaminediacetic acid (EDDA), (C) tricine and trisodium triphenylphosphinetrisulfonate (TPPTS), (D) tricine and nicotinic acid (NIC), or (E) tricine and isonicotinic acid (ISONIC). Isonicotinic Acids 250-267 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11877327-9 2002 Both UTP and 2MeSADP increased the potency and magnitude of IL-8-mediated [Ca(2+)](i) elevation but the effects of UTP (E(max) of IL-8 response increased to 50 +/- 1% of the maximal response to ATP, pEC(50) increased to 9.8 +/- 0.1) were greater than those of 2MeSADP (E(max) increased to 36 +/- 2%, pEC(50) increased to 8.7 +/- 0.2). Uridine Triphosphate 5-8 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 11906276-16 2002 IL-8 can be rapidly and easily labeled with (99m)Tc using HYNIC as a chelator in combination with various coligands. Technetium 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11877327-9 2002 Both UTP and 2MeSADP increased the potency and magnitude of IL-8-mediated [Ca(2+)](i) elevation but the effects of UTP (E(max) of IL-8 response increased to 50 +/- 1% of the maximal response to ATP, pEC(50) increased to 9.8 +/- 0.1) were greater than those of 2MeSADP (E(max) increased to 36 +/- 2%, pEC(50) increased to 8.7 +/- 0.2). methylthio-ADP 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 11877327-9 2002 Both UTP and 2MeSADP increased the potency and magnitude of IL-8-mediated [Ca(2+)](i) elevation but the effects of UTP (E(max) of IL-8 response increased to 50 +/- 1% of the maximal response to ATP, pEC(50) increased to 9.8 +/- 0.1) were greater than those of 2MeSADP (E(max) increased to 36 +/- 2%, pEC(50) increased to 8.7 +/- 0.2). Uridine Triphosphate 115-118 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 11877327-9 2002 Both UTP and 2MeSADP increased the potency and magnitude of IL-8-mediated [Ca(2+)](i) elevation but the effects of UTP (E(max) of IL-8 response increased to 50 +/- 1% of the maximal response to ATP, pEC(50) increased to 9.8 +/- 0.1) were greater than those of 2MeSADP (E(max) increased to 36 +/- 2%, pEC(50) increased to 8.7 +/- 0.2). Adenosine Triphosphate 194-197 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 11877327-12 2002 The potentiation of IL-8-mediated Ca(2+) signalling by UTP was not dependent upon the time of IL-8 addition following UTP but was dependent on the continued presence of UTP. Uridine Triphosphate 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 11877327-12 2002 The potentiation of IL-8-mediated Ca(2+) signalling by UTP was not dependent upon the time of IL-8 addition following UTP but was dependent on the continued presence of UTP. Uridine Triphosphate 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 11877327-12 2002 The potentiation of IL-8-mediated Ca(2+) signalling by UTP was not dependent upon the time of IL-8 addition following UTP but was dependent on the continued presence of UTP. Uridine Triphosphate 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 11882700-3 2002 This study shows that treatment of human intestinal epithelial T84 cells with Etx induces expression of IL-6, IL-10, IL-1R antagonist, as well as IL-1alpha and IL-1beta and low levels of IL-8. 2-ethoxyethanol 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 11966773-8 2002 The MAPK p38 appears necessary for the regulation of IL-8, GRO-alpha and GRO-beta expression as shown by inhibition with SB203580. SB 203580 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 11966773-9 2002 The inhibitors genistein (tyrosine kinase inhibitor) and calphostin C (inhibitor of protein kinase C) reduced significantly the IL-17-stimulated mRNA expression of IL-8, GRO-alpha and GRO-beta in SFC, whereas PD98059 (inhibitor of MEK-1/2) was without effect. Genistein 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 11966773-9 2002 The inhibitors genistein (tyrosine kinase inhibitor) and calphostin C (inhibitor of protein kinase C) reduced significantly the IL-17-stimulated mRNA expression of IL-8, GRO-alpha and GRO-beta in SFC, whereas PD98059 (inhibitor of MEK-1/2) was without effect. calphostin C 57-69 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 11966773-9 2002 The inhibitors genistein (tyrosine kinase inhibitor) and calphostin C (inhibitor of protein kinase C) reduced significantly the IL-17-stimulated mRNA expression of IL-8, GRO-alpha and GRO-beta in SFC, whereas PD98059 (inhibitor of MEK-1/2) was without effect. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 209-216 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 11966773-10 2002 Pharmacological drugs used in therapy of RA, such as cyclosporin and methotrexate, induced a fourfold increase of IL-17R mRNA expression and augmented the IL-17-stimulated IL-8 expression. Cyclosporine 53-64 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 11966773-10 2002 Pharmacological drugs used in therapy of RA, such as cyclosporin and methotrexate, induced a fourfold increase of IL-17R mRNA expression and augmented the IL-17-stimulated IL-8 expression. Methotrexate 69-81 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 11954986-5 2002 RESULTS: Levels of IL-6 and IL-8 significantly increased in subjects with high urine Cr concentration, but TNF-alpha levels decreased. Chromium 85-87 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 11876744-0 2002 Lidocaine inhibits secretion of IL-8 and IL-1beta and stimulates secretion of IL-1 receptor antagonist by epithelial cells. Lidocaine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 11914967-3 2002 LPS-stimulated cells treated with 0.1 microg/ml bisbenzylisoquinoline alkaloid fraction exhibited a 40% inhibition of IL-8 production in comparison with control cells. bisbenzylisoquinoline alkaloid 48-78 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 11814358-3 2002 The binding affinities, obtained by isothermal fluorescence titration, of size-defined heparin and HS oligosaccharides to the chemokine were found to depend on the oligomerization state of IL-8: high affinity was detected for monomeric and low affinity was detected for dimeric IL-8, referring to a self-regulatory mechanism for its chemoattractant effect. hs oligosaccharides 99-118 C-X-C motif chemokine ligand 8 Homo sapiens 278-282 11814358-6 2002 Instead, a periodic pattern was obtained for the dissociation constants of the GAG oligosaccharides with respect to chain length, referring to optimum and least optimum chain lengths for IL-8 binding. gag oligosaccharides 79-99 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 11814358-9 2002 Thermal unfolding of IL-8 yielded a single transition at 56 degrees C which was completely prevented by the presence of undigested HS or heparin, indicating structural stabilization, thereby prolonging the biological effect of the chemokine. Heparitin Sulfate 131-133 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 11814358-9 2002 Thermal unfolding of IL-8 yielded a single transition at 56 degrees C which was completely prevented by the presence of undigested HS or heparin, indicating structural stabilization, thereby prolonging the biological effect of the chemokine. Heparin 137-144 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 11806993-8 2002 Calcium mobilization was studied in neutrophils upon activation with formyl-Met-Leu-Phe (fMLP), adenosine diphosphate (ADP), platelet-activating factor (PAF), interleukin-8 (IL-8), C5a, and leukotriene B(4) (LTB(4)), and it was normal. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 159-172 11806993-8 2002 Calcium mobilization was studied in neutrophils upon activation with formyl-Met-Leu-Phe (fMLP), adenosine diphosphate (ADP), platelet-activating factor (PAF), interleukin-8 (IL-8), C5a, and leukotriene B(4) (LTB(4)), and it was normal. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 11846460-2 2002 We also demonstrated that Tau-Cl suppressed superoxide anion, IL-6, and IL-8 production in activated human polymorphonuclear leukocytes separated from peripheral blood. N-chlorotaurine 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 11814358-0 2002 Different affinities of glycosaminoglycan oligosaccharides for monomeric and dimeric interleukin-8: a model for chemokine regulation at inflammatory sites. glycosaminoglycan oligosaccharides 24-58 C-X-C motif chemokine ligand 8 Homo sapiens 85-98 11814358-1 2002 The binding of interleukin-8 (IL-8) to heparan sulfate (HS) proteoglycans on the surface of endothelial cells is crucial for the recruitment of neutrophils to an inflammatory site. Heparitin Sulfate 39-54 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 11814358-1 2002 The binding of interleukin-8 (IL-8) to heparan sulfate (HS) proteoglycans on the surface of endothelial cells is crucial for the recruitment of neutrophils to an inflammatory site. Heparitin Sulfate 39-54 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 11814358-1 2002 The binding of interleukin-8 (IL-8) to heparan sulfate (HS) proteoglycans on the surface of endothelial cells is crucial for the recruitment of neutrophils to an inflammatory site. Heparitin Sulfate 56-58 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 11814358-1 2002 The binding of interleukin-8 (IL-8) to heparan sulfate (HS) proteoglycans on the surface of endothelial cells is crucial for the recruitment of neutrophils to an inflammatory site. Heparitin Sulfate 56-58 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 11814358-3 2002 The binding affinities, obtained by isothermal fluorescence titration, of size-defined heparin and HS oligosaccharides to the chemokine were found to depend on the oligomerization state of IL-8: high affinity was detected for monomeric and low affinity was detected for dimeric IL-8, referring to a self-regulatory mechanism for its chemoattractant effect. Heparin 87-94 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 11814358-3 2002 The binding affinities, obtained by isothermal fluorescence titration, of size-defined heparin and HS oligosaccharides to the chemokine were found to depend on the oligomerization state of IL-8: high affinity was detected for monomeric and low affinity was detected for dimeric IL-8, referring to a self-regulatory mechanism for its chemoattractant effect. Heparin 87-94 C-X-C motif chemokine ligand 8 Homo sapiens 278-282 11814358-3 2002 The binding affinities, obtained by isothermal fluorescence titration, of size-defined heparin and HS oligosaccharides to the chemokine were found to depend on the oligomerization state of IL-8: high affinity was detected for monomeric and low affinity was detected for dimeric IL-8, referring to a self-regulatory mechanism for its chemoattractant effect. hs oligosaccharides 99-118 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 11846460-6 2002 Production of IL-6, IL-8, and IL-2 in PHA-activated nonadherent leukocytes was inhibited by Tau-Cl. N-chlorotaurine 92-98 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 11846460-7 2002 The production of IL-1beta, IL-6, and IL-8 was also decreased in LPS-activated adherent monocytes by Tau-Cl. N-chlorotaurine 101-107 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 11876744-7 2002 In further experiments, the effect of lidocaine on the secretion of IL-8 from freshly isolated epithelial cells stimulated with TNFalpha was tested. Lidocaine 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 11876744-8 2002 Lidocaine, in therapeutic concentrations, inhibited the spontaneous and TNFalpha-stimulated secretion of IL-8 and IL-1beta from HT-29 and Caco-2 cell lines in a dose-dependent manner. Lidocaine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 11972286-0 2002 alpha-Tocopherol Inhibits IL-8 synthesis induced by thrombin and high glucose in endothelial cells. alpha-Tocopherol 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 11855542-6 2002 The mucosal production of RANTES, interleukin-8, and TNF-alpha showed a significant decrease after eradication in patients with rebamipide after-treatment. rebamipide 128-138 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 11972286-0 2002 alpha-Tocopherol Inhibits IL-8 synthesis induced by thrombin and high glucose in endothelial cells. Glucose 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 12022438-2 2002 Here we report the inhibitory effects of 1alpha,25-dihydroxyvitamin D3 (1,25(OH)2D3) on IL-8 production in human whole blood culture. 1alpha,25-dihydroxyvitamin d3 (1,25(oh)2d3 41-83 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 12022438-3 2002 1,25(OH)2D3 inhibited only the late phase of the biphasic IL-8 production in lipopolysaccharide-stimulated human whole blood. Calcitriol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 11972286-3 2002 Therefore, we examined the effect of alpha-tocopherol on the regulation of IL-8 synthesis induced by high glucose and/or thrombin in endothelial cells. alpha-Tocopherol 37-53 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 12022438-6 2002 Although monocytes were found to be mainly responsible for IL-1beta-induced IL-8 production in whole blood, 1,25(OH)2D3 inhibited IL-8 production by isolated mononuclear cells only marginally. Calcitriol 108-119 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 11972286-3 2002 Therefore, we examined the effect of alpha-tocopherol on the regulation of IL-8 synthesis induced by high glucose and/or thrombin in endothelial cells. Glucose 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 12022438-8 2002 These results suggest that erythrocytes play a role in mediating the inhibitory effects of 1,25(OH)2D3 on IL-8 production in IL-1beta-stimulated whole blood. Calcitriol 91-102 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 11972286-5 2002 Furthermore, high glucose levels and thrombin combined had additive effects on IL-8 synthesis, and alpha-tocopherol diminished their effect; alpha-tocopherol also inhibited the phosphorylation of IkappaB-alpha induced by high glucose levels and/or thrombin. Glucose 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 11972286-5 2002 Furthermore, high glucose levels and thrombin combined had additive effects on IL-8 synthesis, and alpha-tocopherol diminished their effect; alpha-tocopherol also inhibited the phosphorylation of IkappaB-alpha induced by high glucose levels and/or thrombin. alpha-Tocopherol 141-157 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 11972286-6 2002 Our results suggest that the administration of alpha-tocopherol to diabetic patients may have a beneficial effect for the prevention of diabetic vascular complications by the inhibition of IL-8 synthesis from endothelial cells. alpha-Tocopherol 47-63 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 12022438-0 2002 1 alpha,25-dihydroxyvitamin D3 suppresses interleukin-1beta-induced interleukin-8 production in human whole blood: an involvement of erythrocytes in the inhibition. Calcitriol 0-30 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 11880144-1 2002 We show that treatment of cerebellar granules with interleukin-8 (IL-8), growth-related gene product beta (GRObeta) or AMPA induced activation of PI3-K/Akt and of ERK pathways, the latter being independent of PI3-K and dependent on PTX-sensitive G proteins. ptx 232-235 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 11801678-0 2002 15-deoxy-Delta 12,14-PGJ2 induces IL-8 production in human T cells by a mitogen-activated protein kinase pathway. 15-deoxy-delta(12,14)-prostaglandin J2 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 11801678-9 2002 In this study, we report that 15-d-PGJ(2) induced a significant increase in both IL-8 mRNA and protein from activated human T lymphocytes. 15-d-pgj 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 11801678-10 2002 The induction of IL-8 by 15-d-PGJ(2) did not occur through the nuclear receptor PPAR-gamma, as synthetic PPAR-gamma agonists did not mimic the IL-8-inducing effects of 15-d-PGJ(2). 15-d-pgj 25-33 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11911801-6 2002 In contrast, preincubation of the monocytes with the protein tyrosine kinase (PTK) inhibitor genistein resulted in dose-dependent suppression of mycobacteria-induced CXCL-8 secretion. Genistein 93-102 C-X-C motif chemokine ligand 8 Homo sapiens 166-172 11911801-7 2002 These results were further supported by the fact that treatment of monocytes with herbimycin-A, another well-described inhibitor of PTK activity with a different mechanism of action, significantly diminished the effect of M. bovis on CXCL-8 secretion. herbimycin 82-94 C-X-C motif chemokine ligand 8 Homo sapiens 234-240 11911801-10 2002 Finally, two specific NF-kappa B inhibitors, sulfasalazine and caffeic acid phenetyl ester (CAPE), strongly inhibited the production of CXCL-8 by human monocytes infected with M. bovis. Sulfasalazine 45-58 C-X-C motif chemokine ligand 8 Homo sapiens 136-142 11911801-10 2002 Finally, two specific NF-kappa B inhibitors, sulfasalazine and caffeic acid phenetyl ester (CAPE), strongly inhibited the production of CXCL-8 by human monocytes infected with M. bovis. caffeic acid phenetyl ester 63-90 C-X-C motif chemokine ligand 8 Homo sapiens 136-142 11911801-10 2002 Finally, two specific NF-kappa B inhibitors, sulfasalazine and caffeic acid phenetyl ester (CAPE), strongly inhibited the production of CXCL-8 by human monocytes infected with M. bovis. caffeic acid phenethyl ester 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 136-142 11880144-1 2002 We show that treatment of cerebellar granules with interleukin-8 (IL-8), growth-related gene product beta (GRObeta) or AMPA induced activation of PI3-K/Akt and of ERK pathways, the latter being independent of PI3-K and dependent on PTX-sensitive G proteins. ptx 232-235 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 12774392-2 2002 METHOD: The amounts of IFN-alpha, IFN-gamma, TNF-alpha, IL-8 in the peripheral blood mononuclear cells(PBMCs) culture supernatants deal with by different concentrations of LianBiZhi (LBZ) injection made of andrographolide were detected by biological activity test or ELISA in vitro. lianbizhi 172-181 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 12774392-2 2002 METHOD: The amounts of IFN-alpha, IFN-gamma, TNF-alpha, IL-8 in the peripheral blood mononuclear cells(PBMCs) culture supernatants deal with by different concentrations of LianBiZhi (LBZ) injection made of andrographolide were detected by biological activity test or ELISA in vitro. lbz 183-186 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 11782202-5 2002 The FB1-cholesterol complex was reinforced by NaCl but was destabilized by NaF, a salt known to break hydrogen bonds. Cholesterol 8-19 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 11782202-5 2002 The FB1-cholesterol complex was reinforced by NaCl but was destabilized by NaF, a salt known to break hydrogen bonds. Hydrogen 102-110 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 11807693-6 2002 GBS invasion and IL-8 induction were significantly reduced in the presence of dipalmotyl phosphatidylcholine, a major constituent of lung surfactant and a known inhibitor of beta-h/c activity. dipalmotyl phosphatidylcholine 78-108 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11790657-5 2002 IL-8 levels after 2 h of reperfusion correlated with lung function assessed by the Pa(O2 )/FI(O(2)) ratio, the mean airway pressure, and the APACHE score during the first 24 postoperative hours. o2 ) 86-90 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11777986-10 2002 Furthermore, intracellularly delivered dexamethasone was able to down-regulate the proinflammatory gene IL-8. Dexamethasone 39-52 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 11755918-0 2002 Upregulation of interleukin-8 expression by prostaglandin D2 metabolite 15-deoxy-delta12, 14 prostaglandin J2 (15d-PGJ2) in human THP-1 macrophages. Prostaglandin D2 44-60 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 12136943-7 2002 They appeared to undergo a change in the phenotype induced by NaB, as indicated by reduced proliferation, enhanced differentiation, stimulation of apoptosis leading to decreased viability of cells, and stimulation of interleukin-8 secretion. nab 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 217-230 11755918-0 2002 Upregulation of interleukin-8 expression by prostaglandin D2 metabolite 15-deoxy-delta12, 14 prostaglandin J2 (15d-PGJ2) in human THP-1 macrophages. 15-deoxy-delta12 72-88 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 11755918-0 2002 Upregulation of interleukin-8 expression by prostaglandin D2 metabolite 15-deoxy-delta12, 14 prostaglandin J2 (15d-PGJ2) in human THP-1 macrophages. 9-deoxy-delta-9-prostaglandin D2 93-109 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 11755918-2 2002 The expression of IL-8 gene can be induced in cholesterol loaded THP-1 macrophages by oxidized low density lipoprotein. Cholesterol 46-57 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 11755918-3 2002 We report for the first time that the expression of human IL-8 gene in THP-1 macrophages is upregulated in a time- and concentration-dependent manner by prostaglandin D2 metabolite 15-deoxy-delta12, 14 prostaglandin J2 (15d-PGJ2), which is a natural ligand for activation of peroxisome proliferator-activated receptor-gamma transcription factor. Prostaglandin D2 153-169 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 11755918-3 2002 We report for the first time that the expression of human IL-8 gene in THP-1 macrophages is upregulated in a time- and concentration-dependent manner by prostaglandin D2 metabolite 15-deoxy-delta12, 14 prostaglandin J2 (15d-PGJ2), which is a natural ligand for activation of peroxisome proliferator-activated receptor-gamma transcription factor. 15-deoxy-delta12 181-197 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 11755918-3 2002 We report for the first time that the expression of human IL-8 gene in THP-1 macrophages is upregulated in a time- and concentration-dependent manner by prostaglandin D2 metabolite 15-deoxy-delta12, 14 prostaglandin J2 (15d-PGJ2), which is a natural ligand for activation of peroxisome proliferator-activated receptor-gamma transcription factor. 9-deoxy-delta-9-prostaglandin D2 202-218 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 11762855-8 2002 When the NaF concentration was lower than 0.10%, the Rp value (> 3.4 x 10(5) omega cm2) was mainly ascribed to the formation of a protective titanium dioxide (TiO2) on the metal surface, regardless of the elastic tensile strain applied. titanium dioxide 144-160 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 11824547-0 2002 Synergistic action of beta-glucan and platelets on interleukin-8 production by human peripheral blood leukocytes. beta-Glucans 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 11762855-8 2002 When the NaF concentration was lower than 0.10%, the Rp value (> 3.4 x 10(5) omega cm2) was mainly ascribed to the formation of a protective titanium dioxide (TiO2) on the metal surface, regardless of the elastic tensile strain applied. titanium dioxide 162-166 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 11755918-3 2002 We report for the first time that the expression of human IL-8 gene in THP-1 macrophages is upregulated in a time- and concentration-dependent manner by prostaglandin D2 metabolite 15-deoxy-delta12, 14 prostaglandin J2 (15d-PGJ2), which is a natural ligand for activation of peroxisome proliferator-activated receptor-gamma transcription factor. 15-deoxy-delta(12,14)-prostaglandin J2 220-228 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 11762855-8 2002 When the NaF concentration was lower than 0.10%, the Rp value (> 3.4 x 10(5) omega cm2) was mainly ascribed to the formation of a protective titanium dioxide (TiO2) on the metal surface, regardless of the elastic tensile strain applied. Metals 175-180 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 11755918-4 2002 Studies to identify the signal transduction pathways involved showed that IL-8 upregulation-mediated by 15d-PGJ2 was markedly inhibited when the THP-1 macrophages were incubated with a highly selective and cell-permeable inhibitor of the mitogen-activated protein kinase (MAPK) signaling pathway, 2"-amino-3"-methoxyflavone (PD98059). 15-deoxy-delta(12,14)-prostaglandin J2 104-112 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 11762855-9 2002 However, when the NaF concentration was higher than 0.1%, the protectiveness of TiO2 was destroyed by fluoride ions, leading to severe corrosion of CP titanium. titanium dioxide 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 11762855-9 2002 However, when the NaF concentration was higher than 0.1%, the protectiveness of TiO2 was destroyed by fluoride ions, leading to severe corrosion of CP titanium. Fluorides 102-110 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 11755918-4 2002 Studies to identify the signal transduction pathways involved showed that IL-8 upregulation-mediated by 15d-PGJ2 was markedly inhibited when the THP-1 macrophages were incubated with a highly selective and cell-permeable inhibitor of the mitogen-activated protein kinase (MAPK) signaling pathway, 2"-amino-3"-methoxyflavone (PD98059). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 297-323 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 11755918-4 2002 Studies to identify the signal transduction pathways involved showed that IL-8 upregulation-mediated by 15d-PGJ2 was markedly inhibited when the THP-1 macrophages were incubated with a highly selective and cell-permeable inhibitor of the mitogen-activated protein kinase (MAPK) signaling pathway, 2"-amino-3"-methoxyflavone (PD98059). 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 325-332 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 11755918-5 2002 This inhibition was concentration-dependent, suggesting that 15d-PGJ2 regulates the expression of IL-8 gene in THP-1 macrophages through a MAPK signaling pathway. 15-deoxy-delta(12,14)-prostaglandin J2 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 11755918-6 2002 In contrast, THP-1 macrophages when treated with pyrrolidine dithiocarbamate, an anti-oxidant and the selective inhibitor for nuclear factor kappaB, showed an enhanced 15d-PGJ2-mediated upregulation of IL-8 gene expression. pyrrolidine dithiocarbamic acid 49-76 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 11755918-6 2002 In contrast, THP-1 macrophages when treated with pyrrolidine dithiocarbamate, an anti-oxidant and the selective inhibitor for nuclear factor kappaB, showed an enhanced 15d-PGJ2-mediated upregulation of IL-8 gene expression. 9-deoxy-delta-9-prostaglandin D2 171-176 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 12090473-6 2002 Both cytokines enhanced the ability of the cells to adhere to the CD44-specific ligand hyaluronic acid, an effect that was specifically blocked by an anti-IL-8 antibody. Hyaluronic Acid 87-102 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 12666825-5 2002 There were positive important correlations between plasma selenium and IL-2r, copper and IL-6, and copper and IL-1beta, and negative correlations between selenium and IL-8, iron and TNF-alpha, and zinc and IL-1beta contents in patients with CL. Selenium 154-162 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 11841414-6 2002 IL-8 concentrations were weakly correlated with age, male sex, and concentrations of C-reactive protein, factor VIII coagulation activity and homocysteine, but adjustment for these factors did not substantially affect the association between IL-8 and venous thrombosis. Homocysteine 142-154 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 12083423-0 2002 Suppression of sulfur mustard-increased IL-8 in human keratinocyte cell cultures by serine protease inhibitors: implications for toxicity and medical countermeasures. Mustard Gas 15-29 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 12083423-9 2002 The suppression of SM-increased IL-8 by a class of drug candidate compounds such as protease inhibitors may provide a mechanistic marker that helps predict future medical countermeasures for SM toxicity and reduces the need for testing in animal models. Samarium 19-21 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 11789672-8 2002 When M-CSF was added to cultured PBM, the level of IL-8 in the supernatant increased with the concentration of M-CSF. pbm 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 11740968-0 2002 Regulation of NaF release from bis-GMA/TEGDMA resin using gamma-methacryloxypropyltrimethoxysilane. Bisphenol A-Glycidyl Methacrylate 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 11740968-0 2002 Regulation of NaF release from bis-GMA/TEGDMA resin using gamma-methacryloxypropyltrimethoxysilane. triethylene glycol dimethacrylate 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 11740968-0 2002 Regulation of NaF release from bis-GMA/TEGDMA resin using gamma-methacryloxypropyltrimethoxysilane. methacryloxypropyltrimethoxysilane 58-98 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 11740968-1 2002 OBJECTIVES: The aim of this study was to evaluate the feasibility of regulation of NaF release from bis-GMA/TEGDMA resin using gamma-methacryloxypropyltrimethoxysilane (gamma-MPTS). Bisphenol A-Glycidyl Methacrylate 100-107 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 11740968-1 2002 OBJECTIVES: The aim of this study was to evaluate the feasibility of regulation of NaF release from bis-GMA/TEGDMA resin using gamma-methacryloxypropyltrimethoxysilane (gamma-MPTS). triethylene glycol dimethacrylate 108-114 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 11740968-1 2002 OBJECTIVES: The aim of this study was to evaluate the feasibility of regulation of NaF release from bis-GMA/TEGDMA resin using gamma-methacryloxypropyltrimethoxysilane (gamma-MPTS). methacryloxypropyltrimethoxysilane 127-167 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 11740968-1 2002 OBJECTIVES: The aim of this study was to evaluate the feasibility of regulation of NaF release from bis-GMA/TEGDMA resin using gamma-methacryloxypropyltrimethoxysilane (gamma-MPTS). methacryloxypropyltrimethoxysilane 169-179 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 11740968-2 2002 METHODS: NaF powder was treated with gamma-MPTS to form a polysiloxane layer on its surface. methacryloxypropyltrimethoxysilane 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 11740968-2 2002 METHODS: NaF powder was treated with gamma-MPTS to form a polysiloxane layer on its surface. Siloxanes 58-70 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 11740968-4 2002 Bis-GMA/TEGDMA resin containing 50 wt% NaF powder was prepared as a model resin and immersed in distilled water at 37 degrees C, and the amount of fluoride released from the resin was measured using a fluoride electrode. Bisphenol A-Glycidyl Methacrylate 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 11740968-6 2002 RESULTS: NaF powder was covered with hydrophobic gamma-MPTS delivered polysiloxane. methacryloxypropyltrimethoxysilane 49-59 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 11740968-6 2002 RESULTS: NaF powder was covered with hydrophobic gamma-MPTS delivered polysiloxane. Siloxanes 70-82 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 11740968-7 2002 A larger amount of fluoride was released at the initial stage from the resin containing NaF treated with no gamma-MPTS. Fluorides 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 11740968-9 2002 In contrast, we observed a smaller amount of fluoride released for a longer period from the resin containing NaF treated with gamma-MPTS. Fluorides 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 11740968-9 2002 In contrast, we observed a smaller amount of fluoride released for a longer period from the resin containing NaF treated with gamma-MPTS. methacryloxypropyltrimethoxysilane 126-136 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 11740968-10 2002 SIGNIFICANCE: We found that gamma-MPTS treatment is useful for the regulation of NaF release from bis-GMA/TEGDMA resin. methacryloxypropyltrimethoxysilane 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 11740968-10 2002 SIGNIFICANCE: We found that gamma-MPTS treatment is useful for the regulation of NaF release from bis-GMA/TEGDMA resin. Bisphenol A-Glycidyl Methacrylate 98-105 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 11740968-10 2002 SIGNIFICANCE: We found that gamma-MPTS treatment is useful for the regulation of NaF release from bis-GMA/TEGDMA resin. triethylene glycol dimethacrylate 106-112 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 11740968-11 2002 The mechanism of slow NaF release may be the formation of a hydrophobic polysiloxane layer on the surface of NaF powder and resulting slow water diffusion to NaF powder. Siloxanes 72-84 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 11740968-11 2002 The mechanism of slow NaF release may be the formation of a hydrophobic polysiloxane layer on the surface of NaF powder and resulting slow water diffusion to NaF powder. Siloxanes 72-84 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 11740968-11 2002 The mechanism of slow NaF release may be the formation of a hydrophobic polysiloxane layer on the surface of NaF powder and resulting slow water diffusion to NaF powder. Siloxanes 72-84 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 11740968-11 2002 The mechanism of slow NaF release may be the formation of a hydrophobic polysiloxane layer on the surface of NaF powder and resulting slow water diffusion to NaF powder. Water 139-144 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 11789672-9 2002 When IL-8 was added to cultured granulocytes, the levels of CD18 expression on granulocytes and superoxide anion production by granulocytes were significantly increased. Superoxides 96-112 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 11916128-4 2002 We found that histamine significantly augmented the production of IL-6 and IL-8 in a dose- and time-dependent manner. Histamine 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 11916128-0 2002 Histamine-induced IL-6 and IL-8 production are differentially modulated by IFN-gamma and IL-4 in human keratinocytes. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 12182553-6 2002 Induction of interleukin-8 (IL-8) secretion was detected on PAH and PLL ending polyelectrolyte films. polyallylamine 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 12182553-6 2002 Induction of interleukin-8 (IL-8) secretion was detected on PAH and PLL ending polyelectrolyte films. polyallylamine 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 11835523-9 2002 High glucose may stimulate MCP-1 and/or IL-8 production and their excretion into the urine independently of the phases or pathological lesions of this disease. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 11916128-7 2002 The histamine-induced up-regulation of IL-6 and IL-8 production, however, was completely abrogated by a combination of pyrilamine and cimetidine. Histamine 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 11916128-3 2002 We therefore examined the capacity of histamine to modulate the production of interleukin (IL)-6 and IL-8 by keratinocytes. Histamine 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 11916128-7 2002 The histamine-induced up-regulation of IL-6 and IL-8 production, however, was completely abrogated by a combination of pyrilamine and cimetidine. Pyrilamine 119-129 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 11916128-7 2002 The histamine-induced up-regulation of IL-6 and IL-8 production, however, was completely abrogated by a combination of pyrilamine and cimetidine. Cimetidine 134-144 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 11916128-10 2002 On the other hand, the production of IL-8 was inhibited by IFN-gamma, and IFN-gamma and IL-4 both completely abrogated the histamine-induced IL-8 production. Histamine 123-132 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 11916128-10 2002 On the other hand, the production of IL-8 was inhibited by IFN-gamma, and IFN-gamma and IL-4 both completely abrogated the histamine-induced IL-8 production. Histamine 123-132 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 11916128-11 2002 These results suggest that the histamine-induced IL-6 production and IL-8 production are differentially regulated by IFN-gamma and IL-4. Histamine 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 11813828-6 2002 Preincubation with the PKC inhibitor calphostin C (1 microM) significantly suppressed IL-8 release in HBEC treated with CSE and C5a. calphostin C 37-49 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 11813828-7 2002 Preincubation with 10 microM TMB-8 (an intracellular calcium sequester) also significantly suppressed IL-8 release in CSE- and C5a-treated HBEC, suggesting that intracellular calcium is required for CSE- and C5a-mediated IL-8 release. Calcium 175-182 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 11813828-8 2002 When HBEC were preincubated with 30 nM of the PKCbeta-specific inhibitor LY363196, CSE- and C5a-mediated IL-8 release was not inhibited. ly363196 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 11813828-9 2002 However, with higher concentrations of LY363196 (>600 nM), which exceeds the IC50 for PKCbeta greater than 100 fold, CSE- and C5a-mediated IL-8 release was significantly suppressed. ly363196 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 11813828-7 2002 Preincubation with 10 microM TMB-8 (an intracellular calcium sequester) also significantly suppressed IL-8 release in CSE- and C5a-treated HBEC, suggesting that intracellular calcium is required for CSE- and C5a-mediated IL-8 release. 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 11813828-10 2002 Preincubation of HBEC with 100 nM of Go 6976, a specific PKCalpha inhibitor, significantly inhibited CSE- and C5a-mediated stimulation of IL-8 release. Go 6976 37-44 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 11813828-11 2002 CONCLUSIONS: Collectively, these data suggest that PKC activators in addition to CSE augment C5a-stimulated IL-8 release from HBEC and that CSE and C5a stimulate IL-8 release in HBEC by activating the calcium-dependent PKCalpha isoform. Calcium 201-208 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 11813828-7 2002 Preincubation with 10 microM TMB-8 (an intracellular calcium sequester) also significantly suppressed IL-8 release in CSE- and C5a-treated HBEC, suggesting that intracellular calcium is required for CSE- and C5a-mediated IL-8 release. 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 11813828-7 2002 Preincubation with 10 microM TMB-8 (an intracellular calcium sequester) also significantly suppressed IL-8 release in CSE- and C5a-treated HBEC, suggesting that intracellular calcium is required for CSE- and C5a-mediated IL-8 release. Calcium 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 11857718-10 2002 This in turn indicates that the reaction pathway involving only the loss of one or multiple units of BF(3), favored for the (NaBF(4))(n)Na(+) cluster series, but not for the analogous (KBF(4))(n)K(+) series, may be due to the high gas-phase stability of NaF, and relatively lower stability of KF, towards dissociation. boron trifluoride 101-106 C-X-C motif chemokine ligand 8 Homo sapiens 254-257 12424420-3 2002 STUDY DESIGN: The IL-1beta-induced IL-6/IL-8 release of HPMC from healthy donors and from patients with end-stage renal disease (ESRD) were measured before the start of chronic peritoneal dialysis (PD) and during PD therapy. hydroxypropylmethylcellulose-lactose matrix 56-60 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 12424420-12 2002 However, HPMC from uremic patients produced more IL-8 on IL-1beta stimulation than the non-uremic controls (group 2, 53.5 +/- 15.7 pg/microg; group 3, 70.5 +/- 27.3 pg/microg vs. group 1, 24.0 +/- 11.8 pg/microg). hydroxypropylmethylcellulose-lactose matrix 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 12424420-17 2002 Not further classified serum components in uremia also enhance IL-6 and IL-8 release of HPMC. hydroxypropylmethylcellulose-lactose matrix 88-92 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 12090783-0 2002 The selective CXCR2 antagonist SB272844 blocks interleukin-8 and growth-related oncogene-alpha-mediated inhibition of spontaneous neutrophil apoptosis. sb272844 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 12090783-3 2002 The pro-survival effect of a fixed concentration of agonist (IL-8 or Gro-alpha) on cultured neutrophils was abrogated by a selective CXCR2 antagonist SB272844 (K(D)s 253 nM and 49.9 nM in the presence of IL-8 or Gro-alpha respectively). sb272844 150-158 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 12090783-3 2002 The pro-survival effect of a fixed concentration of agonist (IL-8 or Gro-alpha) on cultured neutrophils was abrogated by a selective CXCR2 antagonist SB272844 (K(D)s 253 nM and 49.9 nM in the presence of IL-8 or Gro-alpha respectively). sb272844 150-158 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 12090783-5 2002 The inhibitory effect of IL-8 may in addition partly be mediated through CXCR1 as SB272844 was less potent in its ability to abrogate the anti-apoptotic effects of IL-8 when this agent was used as an agonist. sb272844 82-90 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 12090783-5 2002 The inhibitory effect of IL-8 may in addition partly be mediated through CXCR1 as SB272844 was less potent in its ability to abrogate the anti-apoptotic effects of IL-8 when this agent was used as an agonist. sb272844 82-90 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 12477328-4 2002 IL-8 and TNF-alpha were visualized by means of immunohistochemistry in paraffin-embedded heart valve biopsies from 6 patients with infective endocarditis who required cardiac surgery during the active phase of the infection. Paraffin 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 15526538-6 2002 The potent proinflammatory cytokines IL-1 and TNFalpha and also IL-8 and IFNalpha,gamma stimulate cells in different tissues to release harmful proteinases and reactive oxygen species, contributing to tissue damage. Reactive Oxygen Species 160-183 C-X-C motif chemokine ligand 8 Homo sapiens 64-81 12688521-7 2002 This IL-8 production was inhibited by catechins. Catechin 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 11848444-8 2002 Furthermore, ELISA assays performed on the supernatant of HUVEC culture medium showed a significant increase of IL-8 for cells treated with 25-mM compared to 5-mM glucose. Glucose 163-170 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 11751182-5 2001 Budesonide treatment did not inhibit the functional response to ozone exposure, as determined by reduction in FEV(1) and increase in total symptom score, but it significantly blunted the increase in the percentage of sputum neutrophils and interleukin-8 concentrations in the supernatant (p < 0.05). Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 240-253 11766169-4 2001 In the absence of LPS, DON at 500 or 1,000 ng/ml upregulated TNF-alpha production as early as 3 h and up to 6 h, whereas 100 to 1,000 ng/ml of DON significantly increased production of IL-6 from 3 to 24 h and IL-8 from 6 to 48 h. In cells costimulated with 0.2 microg/ml LPS, DON at 500 or 1000 ng/ml markedly superinduced TNF-alpha and IL-8 production. DONS 143-146 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 11766169-4 2001 In the absence of LPS, DON at 500 or 1,000 ng/ml upregulated TNF-alpha production as early as 3 h and up to 6 h, whereas 100 to 1,000 ng/ml of DON significantly increased production of IL-6 from 3 to 24 h and IL-8 from 6 to 48 h. In cells costimulated with 0.2 microg/ml LPS, DON at 500 or 1000 ng/ml markedly superinduced TNF-alpha and IL-8 production. DONS 143-146 C-X-C motif chemokine ligand 8 Homo sapiens 337-341 11766169-6 2001 Four other 8-ketotrichothecenes, fusarenon X, nivalenol, 3-acetyl DON, and 15-acetyl DON, were also capable of upregulating or suppressing TNF-alpha, IL-6, and IL-8 production at concentrations similar to that of DON. 8-ketotrichothecenes 11-31 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 11766169-6 2001 Four other 8-ketotrichothecenes, fusarenon X, nivalenol, 3-acetyl DON, and 15-acetyl DON, were also capable of upregulating or suppressing TNF-alpha, IL-6, and IL-8 production at concentrations similar to that of DON. 3-Acetyldeoxynivalenol 57-69 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 11766169-6 2001 Four other 8-ketotrichothecenes, fusarenon X, nivalenol, 3-acetyl DON, and 15-acetyl DON, were also capable of upregulating or suppressing TNF-alpha, IL-6, and IL-8 production at concentrations similar to that of DON. ZINC33650233 75-88 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 11766169-0 2001 Differential upregulation of TNF-alpha, IL-6, and IL-8 production by deoxynivalenol (vomitoxin) and other 8-ketotrichothecenes in a human macrophage model. deoxynivalenol 69-83 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 11766169-0 2001 Differential upregulation of TNF-alpha, IL-6, and IL-8 production by deoxynivalenol (vomitoxin) and other 8-ketotrichothecenes in a human macrophage model. deoxynivalenol 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 11766169-0 2001 Differential upregulation of TNF-alpha, IL-6, and IL-8 production by deoxynivalenol (vomitoxin) and other 8-ketotrichothecenes in a human macrophage model. 8-ketotrichothecenes 106-126 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 11766169-4 2001 In the absence of LPS, DON at 500 or 1,000 ng/ml upregulated TNF-alpha production as early as 3 h and up to 6 h, whereas 100 to 1,000 ng/ml of DON significantly increased production of IL-6 from 3 to 24 h and IL-8 from 6 to 48 h. In cells costimulated with 0.2 microg/ml LPS, DON at 500 or 1000 ng/ml markedly superinduced TNF-alpha and IL-8 production. DONS 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 11766169-4 2001 In the absence of LPS, DON at 500 or 1,000 ng/ml upregulated TNF-alpha production as early as 3 h and up to 6 h, whereas 100 to 1,000 ng/ml of DON significantly increased production of IL-6 from 3 to 24 h and IL-8 from 6 to 48 h. In cells costimulated with 0.2 microg/ml LPS, DON at 500 or 1000 ng/ml markedly superinduced TNF-alpha and IL-8 production. DONS 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 337-341 11766169-4 2001 In the absence of LPS, DON at 500 or 1,000 ng/ml upregulated TNF-alpha production as early as 3 h and up to 6 h, whereas 100 to 1,000 ng/ml of DON significantly increased production of IL-6 from 3 to 24 h and IL-8 from 6 to 48 h. In cells costimulated with 0.2 microg/ml LPS, DON at 500 or 1000 ng/ml markedly superinduced TNF-alpha and IL-8 production. DONS 143-146 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 11766169-4 2001 In the absence of LPS, DON at 500 or 1,000 ng/ml upregulated TNF-alpha production as early as 3 h and up to 6 h, whereas 100 to 1,000 ng/ml of DON significantly increased production of IL-6 from 3 to 24 h and IL-8 from 6 to 48 h. In cells costimulated with 0.2 microg/ml LPS, DON at 500 or 1000 ng/ml markedly superinduced TNF-alpha and IL-8 production. DONS 143-146 C-X-C motif chemokine ligand 8 Homo sapiens 337-341 11716760-2 2001 Here we show that, although induction with H(2)O(2) gives rise to NF-kappa B nuclear translocation in both lymphocyte (CEM) and monocyte (U937) cells, it leads only to the production of mRNA species encoding interleukin-8 (IL-8) and macrophage inflammatory protein 1 alpha in U937 cells. Hydrogen Peroxide 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 208-221 12005259-9 2001 Curcumin produced significant inhibition of IL-1beta and IL-8 but minimal inhibition of TNFalpha expression by preterm lung inflammatory cells at 20 uM concentrations. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 12005259-10 2001 Adult PBMC expression of IL-8 was significantly inhibited by curcumin at 20 uM concentrations. Curcumin 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 12005259-11 2001 Therefore, curcumin inhibits pro-inflammatory cytokine production (TNFalpha, IL-1beta and IL-8) by lung inflammatory cells ex vivo. Curcumin 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 11603585-9 2001 Fluoride ion uptakes for AH2 were 451 micromol/g NaF, 378 KF, and 318 RbF. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 11716760-2 2001 Here we show that, although induction with H(2)O(2) gives rise to NF-kappa B nuclear translocation in both lymphocyte (CEM) and monocyte (U937) cells, it leads only to the production of mRNA species encoding interleukin-8 (IL-8) and macrophage inflammatory protein 1 alpha in U937 cells. Hydrogen Peroxide 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 11716760-5 2001 The production of IL-8 mRNA in U937 cells is inhibited by the NF-kappa B inhibitors clasto-lactacystin-beta-lactone and E-64D (l-3-trans-ethoxycarbonyloxirane-2-carbonyl-L-leucine-3-methyl amide) but requires protein synthesis de novo. aloxistatin 120-125 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 11716760-5 2001 The production of IL-8 mRNA in U937 cells is inhibited by the NF-kappa B inhibitors clasto-lactacystin-beta-lactone and E-64D (l-3-trans-ethoxycarbonyloxirane-2-carbonyl-L-leucine-3-methyl amide) but requires protein synthesis de novo. l-3-trans-ethoxycarbonyloxirane-2-carbonyl-l-leucine-3-methyl amide 127-194 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 11717194-3 2001 Ligation of adenosine receptors by adenosine or its related analogue, 2-chloroadenosine (2-CADO), N(6)-cyclopentyladenosine (CPA) or CGS21680 synergistically increased IL-1beta-induced IL-6 and IL-8 production. Adenosine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 11737075-2 2001 Furthermore, alveolar macrophages could produce IL-8 subsequent to CD44-hyaluronic acid (HA) interaction. Hyaluronic Acid 72-87 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 11737075-2 2001 Furthermore, alveolar macrophages could produce IL-8 subsequent to CD44-hyaluronic acid (HA) interaction. ha 89-91 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 11544106-4 2001 While it is constitutively detected in human cancer tissues and established cell lines, IL-8 expression is regulated by various tumor microenvironment factors, such as hypoxia, acidosis, nitric oxide, and cell density. Nitric Oxide 187-199 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 11768272-7 2001 The single exception was the chain-breaking antioxidant butylated hydroxyanisole (BHA), which markedly inhibited IL-6 and IL-8 secretion, but had no effect on NF-kappaB activation. Butylated Hydroxyanisole 56-80 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 11768272-7 2001 The single exception was the chain-breaking antioxidant butylated hydroxyanisole (BHA), which markedly inhibited IL-6 and IL-8 secretion, but had no effect on NF-kappaB activation. Butylated Hydroxyanisole 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 11717194-3 2001 Ligation of adenosine receptors by adenosine or its related analogue, 2-chloroadenosine (2-CADO), N(6)-cyclopentyladenosine (CPA) or CGS21680 synergistically increased IL-1beta-induced IL-6 and IL-8 production. 2-Chloroadenosine 89-95 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 11717194-3 2001 Ligation of adenosine receptors by adenosine or its related analogue, 2-chloroadenosine (2-CADO), N(6)-cyclopentyladenosine (CPA) or CGS21680 synergistically increased IL-1beta-induced IL-6 and IL-8 production. N(6)-cyclopentyladenosine 98-123 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 11717194-3 2001 Ligation of adenosine receptors by adenosine or its related analogue, 2-chloroadenosine (2-CADO), N(6)-cyclopentyladenosine (CPA) or CGS21680 synergistically increased IL-1beta-induced IL-6 and IL-8 production. 2-(4-(2-carboxyethyl)phenethylamino)-5'-N-ethylcarboxamidoadenosine 133-141 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 11712075-9 2001 In the human colon cancer cell line HT-29, inosine dose-dependently attenuated the production of IL-8. Inosine 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 11739559-0 2001 Src family protein tyrosine kinase signaling mediates monosodium urate crystal-induced IL-8 expression by monocytic THP-1 cells. Uric Acid 54-70 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 11794696-2 2001 Cytochalasin B also enhanced changes in membrane potential stimulated by FMLP but inhibited those stimulated by IL-8. Cytochalasin B 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 11794696-1 2001 Cytochalasin B, despite its potent enhancing effect on superoxide (O2-) release triggered by N-formyl-methionyl-leucyl-phenylalanine (FMLP) and many other agonists, significantly inhibited O2- release triggered by interleukin 8 (IL-8) and platelet-activating factor in human neutrophils. Cytochalasin B 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 214-227 11794696-1 2001 Cytochalasin B, despite its potent enhancing effect on superoxide (O2-) release triggered by N-formyl-methionyl-leucyl-phenylalanine (FMLP) and many other agonists, significantly inhibited O2- release triggered by interleukin 8 (IL-8) and platelet-activating factor in human neutrophils. Cytochalasin B 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 229-233 11739559-1 2001 Neutrophil-dependent inflammation dependent on monosodium urate (MSU) crystal-induced IL-8 expression occurs in gout. Uric Acid 47-63 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 11739559-1 2001 Neutrophil-dependent inflammation dependent on monosodium urate (MSU) crystal-induced IL-8 expression occurs in gout. Uric Acid 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 11739559-5 2001 IL-8 expression was attenuated more by the Src kinase inhibitor PP1 than by the p70s6k inhibitor rapamycin. Sirolimus 97-106 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11886504-4 2001 Activators for PPAR-alpha (WY-14,643, clofibrate) were shown to reverse ultraviolet-B-light-mediated expression of inflammatory cytokines (interleukin-6, interleukin-8). Clofibrate 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 154-167 11855746-1 2001 This study compared the effects of cholera toxin (CTX) and pertussis toxin (PTX) on the actions of sodium fluoride (NaF) and those of aluminum fluoride (AlF3) on cell proliferation and differentiation, as well as tyrosine phosphorylation level of mitogen activated protein kinase (MAPK) in human bone cells. Sodium Fluoride 99-114 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 11855746-2 2001 NaF and AlF3 each significantly stimulated the proliferation of human TE85 osteosarcoma cells, increased cellular alkaline phosphatase (ALP) activity, and increased MAPK tyrosine phosphorylation level. Tyrosine 170-178 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 11698167-0 2001 Analysis of interleukin-8 release from normal human epidermal keratinocytes exposed to aliphatic hydrocarbons: delivery of hydrocarbons to cell cultures via complexation with alpha-cyclodextrin. Hydrocarbons 97-109 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 11800083-10 2001 Interleukin-8 levels increased significantly after treatment in the plasma exchange group while decreasing significantly after treatment in the plasma exchange + CHDF group. chdf 162-166 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 11698167-0 2001 Analysis of interleukin-8 release from normal human epidermal keratinocytes exposed to aliphatic hydrocarbons: delivery of hydrocarbons to cell cultures via complexation with alpha-cyclodextrin. alpha-cyclodextrin 175-193 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 11698167-3 2001 The objective of this study was to examine the effects of individual hydrocarbon components found in these fuels on IL-8 production by NHEK. Hydrocarbons 69-80 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 11574537-9 2001 In summary, our results demonstrate that NT stimulates calcium-dependent NF-kappaB and Ras-dependent Erk pathways that mediate the release of IL-8 from non-transformed human colonocytes. Calcium 55-62 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 11737818-17 2001 There was a significant increase in IL-1alpha and a directional increase in IL-8 levels in adult skin sites treated with the irritant, sodium lauryl sulfate, even in the absence of visible skin irritation (erythema). Sodium Dodecyl Sulfate 135-156 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 11713107-4 2001 Whereas under basal and stimulatory conditions, the addition of DA to endothelial cells dose-dependently increased IL-8 production, the production of ENA-78 and Gro-alpha was significantly inhibited (P < 0.01). Dopamine 64-66 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 11705449-6 2001 IPDX inhibited NECA (5"-N-ethylcarboxamidoadenosine)-induced interleukin-8 secretion in human mast cells (HMC-1) with a potency close to that determined for A(2B)-mediated cAMP accumulation in HEL cells, thus confirming the role of A(2B) adenosine receptors in mediating human mast cell activation. 3-isobutyl-8-pyrrolidinoxanthine 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 11705449-6 2001 IPDX inhibited NECA (5"-N-ethylcarboxamidoadenosine)-induced interleukin-8 secretion in human mast cells (HMC-1) with a potency close to that determined for A(2B)-mediated cAMP accumulation in HEL cells, thus confirming the role of A(2B) adenosine receptors in mediating human mast cell activation. Adenosine-5'-(N-ethylcarboxamide) 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 11705449-6 2001 IPDX inhibited NECA (5"-N-ethylcarboxamidoadenosine)-induced interleukin-8 secretion in human mast cells (HMC-1) with a potency close to that determined for A(2B)-mediated cAMP accumulation in HEL cells, thus confirming the role of A(2B) adenosine receptors in mediating human mast cell activation. Adenosine-5'-(N-ethylcarboxamide) 21-51 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 11687440-9 2001 Differences between pre-antibiotic and follow-up cytokine/creatinine ratios were significant for IL-1 beta, IL-6, and IL-8 (P < 0.01). Creatinine 58-68 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 11687440-10 2001 Differences between pre-antibiotic and control cytokine/creatinine ratios were also significant for IL-1 beta, IL-6, and IL-8 (P < 0.01). Creatinine 56-66 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 11716205-6 2001 The number of IL-8-positive cells was higher in pSS butthe numbers of IL-4-and IL-5-positive cells were not significantly different between pSS and healthy controls. pss 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 11741401-11 2001 ELISA assays of spent culture media showed increased protein levels of TNF-alpha and IL-8 in HMO6 cells following treatment with Abeta(25-35) or LPS. UNII-042A8N37WH 129-134 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 11831875-5 2001 Addition of the glucocorticoid anti-inflammatory agent hydrocortisone (200-1000 ng/ml) attenuated the production of MIP-1alpha and IL-8 in PIV-infected cells while having minimal to no effect on the production of these mediators from cells infected with RSV. Hydrocortisone 55-69 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 11692108-6 2001 A selective MAP kinase kinase inhibitor, PD98059, inhibited IL-17-induced IL-6 and IL-8. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 41-48 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 11597930-0 2001 Increased transcription of IL-8 in endothelial cells is differentially regulated by TNF-alpha and oxidized phospholipids. Phospholipids 107-120 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 11546678-4 2001 Under these conditions, the maximum cAMP production induced by NaF and forskolin was not significantly different among selected clones, regardless of the receptor expression level. Cyclic AMP 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 11583705-7 2001 PMPs induced interleukin-8 (IL-8), interleukin-1 beta (IL-1 beta), and tumor necrosis factor alpha (TNF alpha) production by THP-1. pmps 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 11567778-0 2001 Mechanisms in fluoride-induced interleukin-8 synthesis in human lung epithelial cells. Fluorides 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 11567778-1 2001 Sodium fluoride (NaF) has previously been reported to induce a strong IL-8 response in human epithelial lung cells (A549) via mechanisms that seem to involve the activation of G proteins. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 11567778-1 2001 Sodium fluoride (NaF) has previously been reported to induce a strong IL-8 response in human epithelial lung cells (A549) via mechanisms that seem to involve the activation of G proteins. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 11567778-9 2001 The NaF-induced IL-8 response was weakly augmented by the PKA stimulator forskolin and the G(i) inhibitor pertussis toxin. Colforsin 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 11567778-9 2001 The NaF-induced IL-8 response was weakly augmented by the PKA stimulator forskolin and the G(i) inhibitor pertussis toxin. Colforsin 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 11567778-10 2001 The PKA inhibitor H89 seemed to reduce the NaF-induced IL-8 response, but the measured effect was not statistically significant. N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 11567778-10 2001 The PKA inhibitor H89 seemed to reduce the NaF-induced IL-8 response, but the measured effect was not statistically significant. N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 11567778-14 2001 Tyrosine kinases, Ca(2+)-linked pathways, PI-3 kinase, PKA and phosphatase inhibition seem to play no or minor roles in the fluoride-induced IL-8 response. Fluorides 124-132 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 11749774-12 2001 After administration of methylprednisolone or aprotinin, leukocyte CD11b expression, plasma IL-6, IL-8, C-reactive protein levels, and MPO activity decreased by different extent. Methylprednisolone 24-42 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 11594953-7 2001 Interleukin 6 and IL-8 were increased by 10 microg/mL of CsA, whereas transforming growth factor beta, PIIIP, and total protein were unaffected. Cyclosporine 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 11583705-7 2001 PMPs induced interleukin-8 (IL-8), interleukin-1 beta (IL-1 beta), and tumor necrosis factor alpha (TNF alpha) production by THP-1. pmps 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 11583705-8 2001 PMPs also induced IL-8, IL-1 beta, and interleukin-6 (IL-6) production by ECs. pmps 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 11597930-7 2001 Actinomycin D experiments suggested that both Ox-PAPC and TNF-alpha regulate the expression of IL-8 at the transcriptional level. Dactinomycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 11606315-0 2001 Pravastatin suppresses the interleukin-8 production induced by thrombin in human aortic endothelial cells cultured with high glucose by inhibiting the p44/42 mitogen activated protein kinase. Pravastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 11606315-0 2001 Pravastatin suppresses the interleukin-8 production induced by thrombin in human aortic endothelial cells cultured with high glucose by inhibiting the p44/42 mitogen activated protein kinase. Glucose 125-132 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 11606315-4 2001 Here, we examined the effect of pravastatin, one of the statins, on IL-8 synthesis induced by thrombin in human aortic endothelial cells (AoEC) cultured with high glucose concentrations. Pravastatin 32-43 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 11606315-6 2001 Pravastatin significantly decreased the IL-8 synthesis induced by thrombin. Pravastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 11606315-16 2001 Our results suggest that pravastatin inhibits IL-8 synthesis by blocking the ras-MAP (p44/42) kinase pathway rather than nuclear factor-kappaB. Pravastatin 25-36 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 11606315-17 2001 Pravastatin may prevent atherosclerosis not only by lowering cholesterol levels, but also by suppressing IL-8 synthesis in AoEC through the inhibition of p44/42 MAP kinase, and this may be more beneficial in diabetic patients than in non-diabetics. Pravastatin 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 11566077-3 2001 Studies were performed to measure the effects of fMLP on the synthesis and secretion of IL-8 and mucus by the goblet cell differentiated colon cancer cell lines HT29-MTX (methotrexate-conditioned HT29 colonic adenocarcinoma cell line) and LS174T, and to assess the effects of neutrophil-derived secretagogues on goblet cell secretion in these cell lines. Methotrexate 171-183 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 11566077-4 2001 fMLP (0.1 microM) increased the secretion of IL-8 by 105% (P<0.0001) in HT29-MTX cells and by 401% (P<0.0001) in LS174T cells. Methotrexate 80-83 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 11846989-6 2001 6-Methylcoumarine (weak P) was not cytotoxic, yet it increased IL-8 release and mRNA expression only following UVA irradiation. 6-methylcoumarine 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 11589728-4 2001 Enriched isolated skin mast cells released both TNF-alpha and IL-8 following activation with either anti-IgE, SCF, substance P, compound 48/80 or A23187. Calcimycin 146-152 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11591404-1 2001 OBJECTIVE: To study the effects of omega-3 and omega-6 polyunsaturated fatty acid (PUFA) on in vitro proliferation of endometrial cells and their production of the cytokine interleukin-8 (IL-8). omega-3 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 173-186 11591404-1 2001 OBJECTIVE: To study the effects of omega-3 and omega-6 polyunsaturated fatty acid (PUFA) on in vitro proliferation of endometrial cells and their production of the cytokine interleukin-8 (IL-8). omega-6 polyunsaturated fatty acid 47-81 C-X-C motif chemokine ligand 8 Homo sapiens 173-186 11591404-1 2001 OBJECTIVE: To study the effects of omega-3 and omega-6 polyunsaturated fatty acid (PUFA) on in vitro proliferation of endometrial cells and their production of the cytokine interleukin-8 (IL-8). omega-6 polyunsaturated fatty acid 47-81 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 11591404-1 2001 OBJECTIVE: To study the effects of omega-3 and omega-6 polyunsaturated fatty acid (PUFA) on in vitro proliferation of endometrial cells and their production of the cytokine interleukin-8 (IL-8). Fatty Acids, Unsaturated 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 173-186 11591404-8 2001 Endometrial cells from women with endometriosis secreted higher concentrations of IL-8, especially in the presence of high omega-3:omega-6 PUFA ratios. omega-3 123-130 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 11591404-8 2001 Endometrial cells from women with endometriosis secreted higher concentrations of IL-8, especially in the presence of high omega-3:omega-6 PUFA ratios. omega-6 pufa 131-143 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 11699980-14 2001 Self-applied fluoride therapy should consist of the daily five-minute application of 1.1 percent NaF or APF gel (5,000 ppm of fluoride) in a custom-fitted tray. Fluorides 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 97-100 11688002-16 2001 IL-8 levels in control patients were significantly higher compared with patients treated with aprotinin and patients treated with methylprednisolone 1 hour after CPB (p < 0.05). Methylprednisolone 130-148 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11688002-17 2001 CONCLUSION: This study showed that methylprednisolone suppresses TNF-alpha, IL-6, and IL-8 release; however, aprotinin attenuates IL-8 release alone. Methylprednisolone 35-53 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 11699980-15 2001 For those who cannot tolerate a tray delivery owing to gagging or nausea, a daily 0.05 percent NaF rinse (230 ppm of fluoride) for 1 minute is a less effective alternative. Fluorides 117-125 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 11585641-5 2001 MG-132 inhibited IL-1beta-induced up-regulation of IL-1beta and IL-8 mRNA and protein but increased hypoxia-stimulated expression/release of IL-1beta and IL-8. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 11676825-8 2001 Using enzyme-linked immunosorbent assay, we assessed the effect of glybenclamide on interleukin-8 production in human dermal fibroblasts. Glyburide 67-80 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 11676825-10 2001 Glybenclamide disabled this activation loop and significantly reduced interleukin-8. Glyburide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 11585641-5 2001 MG-132 inhibited IL-1beta-induced up-regulation of IL-1beta and IL-8 mRNA and protein but increased hypoxia-stimulated expression/release of IL-1beta and IL-8. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 11676825-11 2001 In human dermal fibroblasts that were stimulated with tumor necrosis factor alpha to reach high interleukin-1 expression levels, glybenclamide similarly suppressed interleukin-8. Glyburide 129-142 C-X-C motif chemokine ligand 8 Homo sapiens 164-177 11598150-7 2001 IL-18 induces IL-8 secretion through NFkappaB because RA synovial fibroblasts pretreated with antisense to NFkappaB p65 oligonucleotide produce a mean of 44% less IL-8 compared with cells pretreated with the control sense oligonucleotide. Oligonucleotides 120-135 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 11676825-15 2001 These results are consistent with glybenclamide preventing externalization of interleukin-1 and subsequent autocrine induction of interleukin-8 in human dermal fibroblasts. Glyburide 34-47 C-X-C motif chemokine ligand 8 Homo sapiens 130-143 11576379-8 2001 In the ARF/HF group, a significantly positive correlation between CL PMN-priming activity and IL-8 concentrations was observed. CHEMBL2332890 66-72 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 11598150-7 2001 IL-18 induces IL-8 secretion through NFkappaB because RA synovial fibroblasts pretreated with antisense to NFkappaB p65 oligonucleotide produce a mean of 44% less IL-8 compared with cells pretreated with the control sense oligonucleotide. Oligonucleotides 120-135 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 11598150-7 2001 IL-18 induces IL-8 secretion through NFkappaB because RA synovial fibroblasts pretreated with antisense to NFkappaB p65 oligonucleotide produce a mean of 44% less IL-8 compared with cells pretreated with the control sense oligonucleotide. Oligonucleotides 222-237 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 11577781-0 2001 Prostaglandin-J2 induces synthesis of interleukin-8 by endothelial cells in a PPAR-gamma-independent manner. 9-deoxy-delta-9-prostaglandin D2 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 11564889-8 2001 Finally, we show that inhibition of HDAC activity with TSA causes an increase in both basal and TNF-induced expression of the NF-kappaB-regulated interleukin-8 (IL-8) gene. trichostatin A 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 146-159 11564889-8 2001 Finally, we show that inhibition of HDAC activity with TSA causes an increase in both basal and TNF-induced expression of the NF-kappaB-regulated interleukin-8 (IL-8) gene. trichostatin A 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 11564889-9 2001 Similar to the wild-type integrated NF-kappaB-dependent reporter, ChIP assays showed that TSA treatment resulted in hyperacetylation of the IL-8 promoter. trichostatin A 90-93 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 11713368-10 2001 High IL-8 levels negatively correlated with PaO2/FiO2 (r = -0.56, P < 0.001). pao2 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 11713368-10 2001 High IL-8 levels negatively correlated with PaO2/FiO2 (r = -0.56, P < 0.001). fio2 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 11719173-5 2001 In stepwise multiple regression analysis, maximum IL-8 values were significantly correlated with maximum TNF-alpha values within post-ROSC 24 h, with the total dose of administered epinephrine and with peripheral neutrophil counts. Epinephrine 181-192 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 11719173-6 2001 It is especially noteworthy that the total dose of epinephrine administered during and after resuscitation markedly influenced the elevation of serum IL-8 after ROSC. Epinephrine 51-62 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 11719173-7 2001 The increases in serum IL-8 induced by excessive administration of epinephrine might be harmful in the ROSC-patients resuscitated after CPA. Epinephrine 67-78 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 11577781-2 2001 We investigated the influence of PPARgamma-ligands, 15-deoxy-delta12,14 prostaglandin-J2 (15d-PGJ2), and ciglitazone, on the generation of interleukin-8 (IL-8) by the human microvascular endothelial cell line (HMEC- 1). 9-deoxy-delta-9-prostaglandin D2 72-88 C-X-C motif chemokine ligand 8 Homo sapiens 139-152 11577781-2 2001 We investigated the influence of PPARgamma-ligands, 15-deoxy-delta12,14 prostaglandin-J2 (15d-PGJ2), and ciglitazone, on the generation of interleukin-8 (IL-8) by the human microvascular endothelial cell line (HMEC- 1). 15-deoxy-delta(12,14)-prostaglandin J2 90-98 C-X-C motif chemokine ligand 8 Homo sapiens 139-152 11577781-2 2001 We investigated the influence of PPARgamma-ligands, 15-deoxy-delta12,14 prostaglandin-J2 (15d-PGJ2), and ciglitazone, on the generation of interleukin-8 (IL-8) by the human microvascular endothelial cell line (HMEC- 1). ciglitazone 105-116 C-X-C motif chemokine ligand 8 Homo sapiens 139-152 11577781-7 2001 15d-PGJ2 potently and dose-dependently increased both the steady-state and LPS-induced generation of IL-8 mRNA and IL-8 protein. 15-deoxy-delta(12,14)-prostaglandin J2 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 11577781-7 2001 15d-PGJ2 potently and dose-dependently increased both the steady-state and LPS-induced generation of IL-8 mRNA and IL-8 protein. 15-deoxy-delta(12,14)-prostaglandin J2 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 11577781-9 2001 We conclude, that 15d-PGJ2 is a potent inducer of IL-8 production and can be a mediator of inflammatory response, but this effect is independent of PPARgamma activation. 15-deoxy-delta(12,14)-prostaglandin J2 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 11461907-4 2001 The data show that stimulation of 16HBE14o(-) cells with NE induced IL-8 protein production and gene expression. 16hbe14o 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 11517438-2 2001 Exposure of HUVECs to ethanol (0.01%-1%) dose-dependently inhibited (by 12%-27%) the release of stem cell factor, granulocyte-macrophage and granulocyte colony-stimulating factors (CSFs), or interleukin (IL)-8, but not of macrophage CSF triggered by lipopolysaccharide (LPS) or IL-1. Ethanol 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 191-209 11587995-5 2001 After budesonide treatment there was a significant decrease in the number of submucosal cells staining for total NF-kappaB, granulocyte macrophage colony-stimulating factor (GM-CSF) and tumor necrosis factor-alpha (TNF-alpha), accompanied by a significant decrease in mucosal eosinophils and expression of vascular cell adhesion molecule-1 (VCAM-1) in the endothelium and interleukin-8 (IL-8) in the epithelium. Budesonide 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 372-385 11551520-5 2001 In the present study, we demonstrated that cepharanthine suppresses the production of inflammatory cytokines and a chemokine, i.e. TNF-alpha, interleukin (IL)-1beta, IL-6, and IL-8, in human monocytic cell cultures, including primary monocyte/macrophage cultures. cepharanthine 43-56 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 11587995-5 2001 After budesonide treatment there was a significant decrease in the number of submucosal cells staining for total NF-kappaB, granulocyte macrophage colony-stimulating factor (GM-CSF) and tumor necrosis factor-alpha (TNF-alpha), accompanied by a significant decrease in mucosal eosinophils and expression of vascular cell adhesion molecule-1 (VCAM-1) in the endothelium and interleukin-8 (IL-8) in the epithelium. Budesonide 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 387-391 11535839-1 2001 The Plasmodium falciparum translationally controlled tumor protein (TCTP) is a homolog of the mammalian histamine-releasing factor (HRF), which causes histamine release from human basophils and IL-8 secretion from eosinophils. Histamine 104-113 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 11504702-3 2001 Exposure of freshly isolated human neutrophils to acrolein markedly inhibited spontaneous neutrophil apoptosis as indicated by loss of membrane asymmetry and DNA fragmentation and induced increased neutrophil production of the chemokine interleukin-8 (IL-8). Acrolein 50-58 C-X-C motif chemokine ligand 8 Homo sapiens 237-250 11563737-10 2001 If NaF is not used as a preservative, GHB is produced as an artifact. N-Methyl-3,4-methylenedioxyamphetamine 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 3-6 11500171-6 2001 Cerivastatin [10 pM to 100 microM] decreased leukocyte chemotaxis towards interleukin-8 or RANTES. cerivastatin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 11546726-7 2001 Furthermore, ketamine isomers at concentrations exceeding 500 microM significantly suppressed SEB-induced IL-8 production. Ketamine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 11546726-9 2001 CONCLUSION: This study demonstrated that ketamine isomers suppressed SEB-induced TNF-, IL-6, and IL-8 production in human whole blood. Ketamine 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 11557916-0 2001 Elevation of serum interleukin 8 levels in acetaminophen overdose in children and adolescents. Acetaminophen 43-56 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 11557916-12 2001 CONCLUSIONS: Interleukin 8 elevation in patients with acetaminophen hepatotoxicity corresponds with other common clinical measures that are predictive of hepatocellular injury. Acetaminophen 54-67 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 11597034-8 2001 RANTES and IL-8 had more abundant gene messages in PGN. pgn 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 11520766-10 2001 During the second 10-20 day phase, the level of both IL-6 and IL-8 decreased significantly in the presence of pentoxifylline, the relation between these two cytokines being the inverse of that observed in the absence of the drug. Pentoxifylline 110-124 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11520766-12 2001 CONCLUSION: The addition of pentoxifylline to organ culture media leads, ultimately, to a suppression of IL-6 and IL-8 secretion by corneal tissue. Pentoxifylline 28-42 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 11555581-5 2001 IL-8 antisense oligonucleotides specifically reduced IL-8 mRNA and protein levels and inhibited KS cell growth in a dose-dependent manner. Oligonucleotides 15-31 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11555581-5 2001 IL-8 antisense oligonucleotides specifically reduced IL-8 mRNA and protein levels and inhibited KS cell growth in a dose-dependent manner. Oligonucleotides 15-31 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 11531942-7 2001 IL-8 mRNA accumulation was detected by Northern blot analysis within 2 h of stimulation by the immune complexes and was enhanced by the addition of cycloheximide. Cycloheximide 148-161 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11531942-8 2001 Secretion of IL-8 by C1q-IC stimulated HUVEC was completely blocked by the PTK inhibitor, genistein or the MAPK inhibitor, UO126. Genistein 90-99 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 11531942-8 2001 Secretion of IL-8 by C1q-IC stimulated HUVEC was completely blocked by the PTK inhibitor, genistein or the MAPK inhibitor, UO126. U 0126 123-128 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 11504702-3 2001 Exposure of freshly isolated human neutrophils to acrolein markedly inhibited spontaneous neutrophil apoptosis as indicated by loss of membrane asymmetry and DNA fragmentation and induced increased neutrophil production of the chemokine interleukin-8 (IL-8). Acrolein 50-58 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 11509278-7 2001 Our additional finding was that there was a negative correlation between IL-8 level and hemoglobin saturation with oxygen in coronary sinus blood 10 min after coronary reperfusion. Oxygen 115-121 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 11504702-4 2001 Acrolein (1--50 microM) was found to induce marked activation of extracellular signal-regulated kinase (ERK) and p38 mitogen-activated protein kinases (MAPKs), and inhibition of p38 MAPK activation by SB-203580 prevented acrolein-induced IL-8 release. Acrolein 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 12604011-3 2001 Particular hydroxylation patterns of the B ring of the flavones permit them to inhibit histamine, tryptase, interleukin-6 and interleukin-8 release from human umbilical-cord derived cultured mast cells, as well as from macrophages. Flavones 55-63 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 11589350-8 2001 PBNs are spontaneously activated and undergo a greater motility response to IL-8 and Gro-alpha in CFA. pbns 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 11562079-1 2001 We show that radicicol, an anti-fungal agent, inhibits interleukin-8 (IL-8) production by the human monocyte line THP-1 in response to phorbol-12-myristate-13-acetate/lipopolysaccharide (PMA/LPS). Tetradecanoylphorbol Acetate 187-190 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 11562079-8 2001 PD98059 and SB203580, known as a specific inhibitor of MEKI and p38 kinase, respectively, inhibited IL-8 gene expression showing that both of the kinase pathways are involved in IL-8 regulation in human monocytes. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 11562079-8 2001 PD98059 and SB203580, known as a specific inhibitor of MEKI and p38 kinase, respectively, inhibited IL-8 gene expression showing that both of the kinase pathways are involved in IL-8 regulation in human monocytes. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 11562079-8 2001 PD98059 and SB203580, known as a specific inhibitor of MEKI and p38 kinase, respectively, inhibited IL-8 gene expression showing that both of the kinase pathways are involved in IL-8 regulation in human monocytes. SB 203580 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 11562079-8 2001 PD98059 and SB203580, known as a specific inhibitor of MEKI and p38 kinase, respectively, inhibited IL-8 gene expression showing that both of the kinase pathways are involved in IL-8 regulation in human monocytes. SB 203580 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 11562079-9 2001 Collectively, this series of experiments indicates that radicicol inhibits IL-8 gene expression by blocking ERK1/2 and p38 signaling. monorden 56-65 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 11562079-0 2001 Suppression of IL-8 gene expression by radicicol is mediated through the inhibition of ERK1/2 and p38 signaling and negative regulation of NF-kappaB and AP-1. monorden 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 11562079-1 2001 We show that radicicol, an anti-fungal agent, inhibits interleukin-8 (IL-8) production by the human monocyte line THP-1 in response to phorbol-12-myristate-13-acetate/lipopolysaccharide (PMA/LPS). monorden 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 11562079-1 2001 We show that radicicol, an anti-fungal agent, inhibits interleukin-8 (IL-8) production by the human monocyte line THP-1 in response to phorbol-12-myristate-13-acetate/lipopolysaccharide (PMA/LPS). monorden 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 11562079-1 2001 We show that radicicol, an anti-fungal agent, inhibits interleukin-8 (IL-8) production by the human monocyte line THP-1 in response to phorbol-12-myristate-13-acetate/lipopolysaccharide (PMA/LPS). Tetradecanoylphorbol Acetate 135-166 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 11562079-1 2001 We show that radicicol, an anti-fungal agent, inhibits interleukin-8 (IL-8) production by the human monocyte line THP-1 in response to phorbol-12-myristate-13-acetate/lipopolysaccharide (PMA/LPS). Tetradecanoylphorbol Acetate 135-166 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 11595074-7 2001 The pretreatment with interferon (IFN)-gamma markedly enhanced the effects of Fas Ag stimulation; IFN-gamma pretreatment and Fas Ag stimulation synergistically induced not only apoptosis but also IL-8 and MCP-1 secretion. ammonium ferrous sulfate 125-128 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 11527985-4 2001 However, dieldrin was found to increase human neutrophil superoxide production, RNA synthesis, and proinflammatory cytokine interleukin-8 production. Dieldrin 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 11595074-7 2001 The pretreatment with interferon (IFN)-gamma markedly enhanced the effects of Fas Ag stimulation; IFN-gamma pretreatment and Fas Ag stimulation synergistically induced not only apoptosis but also IL-8 and MCP-1 secretion. ammonium ferrous sulfate 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 11527994-4 2001 Actinomycin D at the beginning of culture inhibited IL-8 mRNA induction, whereas late addition affected IL-8 transcript stability, suggesting gene transcription involvement. Dactinomycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 11509634-0 2001 Fibrinogen induces IL-8 synthesis in human neutrophils stimulated with formyl-methionyl-leucyl-phenylalanine or leukotriene B(4). Leukotriene B4 112-125 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 11522371-8 2001 In summary, other mechanisms than particle-induced ROS formation seem to be responsible for the differential induction of IL-8. Reactive Oxygen Species 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 11527995-4 2001 As a first step, we have studied regulation of interleukin (IL) 8 gene expression after interaction with zymosan or latex. Zymosan 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 47-65 11527995-5 2001 IL-8 secretion was consistently one- or twofold higher after incubation with zymosan than with latex. Zymosan 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11527995-8 2001 The NFkappaB inhibitor gliotoxin abrogated zymosan-induced IL-8 synthesis in peripheral blood monocytes, further demonstrating that the induction of IL-8 mRNA by zymosan is NFkappaB dependent. Gliotoxin 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 11527995-8 2001 The NFkappaB inhibitor gliotoxin abrogated zymosan-induced IL-8 synthesis in peripheral blood monocytes, further demonstrating that the induction of IL-8 mRNA by zymosan is NFkappaB dependent. Gliotoxin 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 11527995-8 2001 The NFkappaB inhibitor gliotoxin abrogated zymosan-induced IL-8 synthesis in peripheral blood monocytes, further demonstrating that the induction of IL-8 mRNA by zymosan is NFkappaB dependent. Zymosan 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 11527995-8 2001 The NFkappaB inhibitor gliotoxin abrogated zymosan-induced IL-8 synthesis in peripheral blood monocytes, further demonstrating that the induction of IL-8 mRNA by zymosan is NFkappaB dependent. Zymosan 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 11527995-8 2001 The NFkappaB inhibitor gliotoxin abrogated zymosan-induced IL-8 synthesis in peripheral blood monocytes, further demonstrating that the induction of IL-8 mRNA by zymosan is NFkappaB dependent. Zymosan 162-169 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 11527995-8 2001 The NFkappaB inhibitor gliotoxin abrogated zymosan-induced IL-8 synthesis in peripheral blood monocytes, further demonstrating that the induction of IL-8 mRNA by zymosan is NFkappaB dependent. Zymosan 162-169 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 11527995-9 2001 SB203580 inhibition of the p38 mitogen-activated protein kinase (MAPK) pathway significantly decreased zymosan-induced IL-8 mRNA accumulation. SB 203580 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 11527995-9 2001 SB203580 inhibition of the p38 mitogen-activated protein kinase (MAPK) pathway significantly decreased zymosan-induced IL-8 mRNA accumulation. Zymosan 103-110 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 11527995-11 2001 These data indicate that p38 MAPK and NFkappaB are critical in controlling zymosan-induced IL-8 secretion. Zymosan 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 11535888-13 2001 At 40 minutes, IL-8 and GROalpha significantly inhibited TNFalpha adherence-dependent peroxide production in normal neutrophils (35% +/- 4% and 45% +/- 3%, respectively; p < 0.05). Peroxides 86-94 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 11517293-0 2001 Ectopic endometrial cells express high concentrations of interleukin (IL)-8 in vivo regardless of the menstrual cycle phase and respond to oestradiol by up-regulating IL-1-induced IL-8 expression in vitro. Estradiol 139-149 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 11517293-7 2001 Furthermore, this study provides evidence that oestradiol indirectly up-regulates the expression by ectopic endometrial cells of IL-8, a cytokine endowed with neutrophil chemotactic and angiogenic properties. Estradiol 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 12536723-9 2001 CONCLUSION: Establishment of cultured HPMCs model will provide the basis of the research in preventment of peritoneal fibrosis and roles of IL-8 in peritoneal dialysis. hpmcs 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 11672576-8 2001 In conclusion, the activation of neutrophils with zymosan leads to the activation of PAF receptors and this is followed by activation of CD11/CD18, phagocytosis of zymosan particles and subsequent interleukin-8 release. Zymosan 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 197-210 12536733-0 2001 [Effects of katamine on cardiopulmonary bypass-induced interleukin-6 and interleukin-8 response and its significance]. katamine 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 12536733-1 2001 OBJECTIVE: To investigate the effects of ketamine on cardiopulmonary bypass-induced IL-6 and IL-8 response. Ketamine 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 12536733-6 2001 CONCLUSIONS: Ketamine is effective to reduce cardiopulmonary bypass-induces IL-6 and IL-8 response and protect reperfusion myocardium. Ketamine 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 11493478-0 2001 Antibodies from patients with heparin-induced thrombocytopenia stimulate monocytic cells to express tissue factor and secrete interleukin-8. Heparin 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 11521757-0 2001 Endogenous nitric oxide inhibits neutrophil adherence to lung epithelial cells to modulate interleukin-8 release. Nitric Oxide 11-23 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 11521757-12 2001 In conclusion, endogenous nitric oxide may play a role in preventing neutrophil adherence to lung epithelial cells, thus modulating concomitant IL-8 release. Nitric Oxide 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 11509327-7 2001 Pretreatment with N-acetyl-cysteine (NAC) (1 to 10 mM) or glutathione (1 to 10 mM) inhibited TNF-alpha-induced activation of NF-kappa B transcriptional activity and IL-8 promoter-mediated reporter gene expression. Acetylcysteine 18-35 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 11435224-4 2001 The mitogen-activated protein kinase/ERK kinase (MEK) activity inhibitor PD-98059 significantly abolished IL-8 released in response to Utah Valley PM, as did the epidermal growth factor (EGF) receptor kinase inhibitor AG-1478. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 11435224-7 2001 These data demonstrate that Utah Valley PM can induce IL-8 expression partially through the activation of the EGF receptor signaling. utah valley pm 28-42 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 11509327-7 2001 Pretreatment with N-acetyl-cysteine (NAC) (1 to 10 mM) or glutathione (1 to 10 mM) inhibited TNF-alpha-induced activation of NF-kappa B transcriptional activity and IL-8 promoter-mediated reporter gene expression. Acetylcysteine 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 11509327-7 2001 Pretreatment with N-acetyl-cysteine (NAC) (1 to 10 mM) or glutathione (1 to 10 mM) inhibited TNF-alpha-induced activation of NF-kappa B transcriptional activity and IL-8 promoter-mediated reporter gene expression. Glutathione 58-69 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 11591115-9 2001 Together, these studies are the first to demonstrate that BCG-induced IL-8 secretion by human monocytes appears to be mediated by intracellular Ca(2+) and is NF-kappaB-dependent and at the same time suggest that production of IL-8 in response to M. bovis BCG can contribute to the initial local and systemic inflammatory response in human tuberculosis. bcg 255-258 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 11468165-5 2001 Using the selective p38 MAPK inhibitor SB203580, there was a significant decrease in thrombin-induced interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) protein production and messenger RNA steady-state levels. SB 203580 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 11468165-5 2001 Using the selective p38 MAPK inhibitor SB203580, there was a significant decrease in thrombin-induced interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) protein production and messenger RNA steady-state levels. SB 203580 39-47 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 11468165-6 2001 In addition, SB203580 decreased IL-8 and MCP-1 production induced by the thrombin receptor-1 agonist peptide (TRAP), suggesting functional links between the thrombin G protein-coupled receptor and the p38 MAPK pathway. SB 203580 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 11591115-2 2001 Because the mechanisms through which Mycobacterium bovis Calmette-Guerin (BCG) induces IL-8 secretion are unknown, the aim of the present study was to characterize the nature of IL-8 production induced by BCG in human monocytes. bcg 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 11591115-2 2001 Because the mechanisms through which Mycobacterium bovis Calmette-Guerin (BCG) induces IL-8 secretion are unknown, the aim of the present study was to characterize the nature of IL-8 production induced by BCG in human monocytes. bcg 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 11591115-2 2001 Because the mechanisms through which Mycobacterium bovis Calmette-Guerin (BCG) induces IL-8 secretion are unknown, the aim of the present study was to characterize the nature of IL-8 production induced by BCG in human monocytes. bcg 205-208 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 11479233-9 2001 Inhibitors of MEK (U0126) and PI3K (LY294002) blocked p42/p44(erk) and Akt, respectively, and partially blocked HGF-induced production of IL-8 and VEGF, whereas the combination of U0126 and LY294002 completely inhibited expression of IL-8 and VEGF by UMSCC-11A. U 0126 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 11479233-9 2001 Inhibitors of MEK (U0126) and PI3K (LY294002) blocked p42/p44(erk) and Akt, respectively, and partially blocked HGF-induced production of IL-8 and VEGF, whereas the combination of U0126 and LY294002 completely inhibited expression of IL-8 and VEGF by UMSCC-11A. U 0126 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 11479233-9 2001 Inhibitors of MEK (U0126) and PI3K (LY294002) blocked p42/p44(erk) and Akt, respectively, and partially blocked HGF-induced production of IL-8 and VEGF, whereas the combination of U0126 and LY294002 completely inhibited expression of IL-8 and VEGF by UMSCC-11A. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 11479233-9 2001 Inhibitors of MEK (U0126) and PI3K (LY294002) blocked p42/p44(erk) and Akt, respectively, and partially blocked HGF-induced production of IL-8 and VEGF, whereas the combination of U0126 and LY294002 completely inhibited expression of IL-8 and VEGF by UMSCC-11A. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 11591115-3 2001 In this study, we found that the induction of IL-8 synthesis was dose- and time-dependent after stimulation with BCG. bcg 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 11511305-11 2001 These data suggest that 17beta-estradiol, progesterone, and dihydrotestosterone suppress the growth of melanoma by inhibiting interleukin-8 production in a receptor-dependent manner. Progesterone 42-54 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 11591115-5 2001 We also determined that BCG-induced IL-8 secretion occurs through a mechanism that requires intracellular calcium and likely involves a calmodulin-sensitive step. bcg 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 11591115-5 2001 We also determined that BCG-induced IL-8 secretion occurs through a mechanism that requires intracellular calcium and likely involves a calmodulin-sensitive step. Calcium 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 11591115-6 2001 Interestingly, BCG-induced secretion of IL-8 from human monocytes resulted from transcriptional up-regulation of the IL-8 gene. bcg 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 11591115-6 2001 Interestingly, BCG-induced secretion of IL-8 from human monocytes resulted from transcriptional up-regulation of the IL-8 gene. bcg 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 11591115-9 2001 Together, these studies are the first to demonstrate that BCG-induced IL-8 secretion by human monocytes appears to be mediated by intracellular Ca(2+) and is NF-kappaB-dependent and at the same time suggest that production of IL-8 in response to M. bovis BCG can contribute to the initial local and systemic inflammatory response in human tuberculosis. bcg 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 11591115-9 2001 Together, these studies are the first to demonstrate that BCG-induced IL-8 secretion by human monocytes appears to be mediated by intracellular Ca(2+) and is NF-kappaB-dependent and at the same time suggest that production of IL-8 in response to M. bovis BCG can contribute to the initial local and systemic inflammatory response in human tuberculosis. bcg 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 11591115-9 2001 Together, these studies are the first to demonstrate that BCG-induced IL-8 secretion by human monocytes appears to be mediated by intracellular Ca(2+) and is NF-kappaB-dependent and at the same time suggest that production of IL-8 in response to M. bovis BCG can contribute to the initial local and systemic inflammatory response in human tuberculosis. bcg 255-258 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 11447173-4 2001 PGP induced a high level of interleukin-8 production at doses of 100 ng/ml and higher in OCT-treated THP-1 cells compared with Salmonella LPS, and the production was significantly inhibited by anti-CD14 and anti-TLR2 but not anti-TLR4 antibodies. pgp 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 28-41 11511305-0 2001 17beta-estradiol, progesterone, and dihydrotestosterone suppress the growth of human melanoma by inhibiting interleukin-8 production. Estradiol 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 11511305-0 2001 17beta-estradiol, progesterone, and dihydrotestosterone suppress the growth of human melanoma by inhibiting interleukin-8 production. Progesterone 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 11511305-0 2001 17beta-estradiol, progesterone, and dihydrotestosterone suppress the growth of human melanoma by inhibiting interleukin-8 production. Dihydrotestosterone 36-55 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 11511305-11 2001 These data suggest that 17beta-estradiol, progesterone, and dihydrotestosterone suppress the growth of melanoma by inhibiting interleukin-8 production in a receptor-dependent manner. Estradiol 24-40 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 11461774-2 2001 We have previously reported that fluoride (NaF) induces apoptosis in HL-60 cells by caspase-3 activation. Fluorides 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 11454909-0 2001 Rebamipide inhibits ceramide-induced interleukin-8 production in Kato III human gastric cancer cells. rebamipide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 11454909-0 2001 Rebamipide inhibits ceramide-induced interleukin-8 production in Kato III human gastric cancer cells. Ceramides 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 11454909-3 2001 We have recently reported that H. pylori-dependent ceramide production may activate nuclear factor-kappaB and mediate interleukin-8 expression in human gastric cancer cell lines. Ceramides 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 118-131 11511305-11 2001 These data suggest that 17beta-estradiol, progesterone, and dihydrotestosterone suppress the growth of melanoma by inhibiting interleukin-8 production in a receptor-dependent manner. Dihydrotestosterone 60-79 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 11454909-4 2001 In this study, we evaluated the effect of rebamipide, an antigastritis and antiulcer agent, on H. pylori-dependent ceramide production and subsequent interleukin-8 expression in Kato III cells. rebamipide 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 11454909-5 2001 Rebamipide inhibited ceramide-induced interleukin-8 expression in a dose-dependent manner. rebamipide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 11511306-0 2001 Gangliosides GD1b, GT1b, and GQ1b suppress the growth of human melanoma by inhibiting interleukin-8 production: the inhibition of adenylate cyclase. Gangliosides 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 86-99 11454909-5 2001 Rebamipide inhibited ceramide-induced interleukin-8 expression in a dose-dependent manner. Ceramides 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 11454909-6 2001 Rebamipide decreased the ceramide-induced increase of the interleukin-8 mRNA level as assessed by Northern blotting. rebamipide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 11511306-8 2001 Cyclic AMP analog dibutyryl cAMP counteracted GD1b, GT1b, and GQ1b-induced inhibition of interleukin-8 production at the levels of protein secretion, mRNA expression, and promoter activity. Cyclic AMP 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 11454909-6 2001 Rebamipide decreased the ceramide-induced increase of the interleukin-8 mRNA level as assessed by Northern blotting. Ceramides 25-33 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 11454909-7 2001 Rebamipide suppressed interleukin-8 gene transcription and nuclear factor-kappaB-dependent transcriptional activity as assessed by luciferase assay. rebamipide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 11511306-8 2001 Cyclic AMP analog dibutyryl cAMP counteracted GD1b, GT1b, and GQ1b-induced inhibition of interleukin-8 production at the levels of protein secretion, mRNA expression, and promoter activity. Cyclic AMP 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 11349132-0 2001 P2Y(6) nucleotide receptor mediates monocyte interleukin-8 production in response to UDP or lipopolysaccharide. Uridine Diphosphate 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 11525435-13 2001 Similar effects were seen when IL-8 production was evaluated following HGF stimulation with high doses of nicotine and E. coli LPS or P gingivalis LPS. Nicotine 106-114 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 11525435-14 2001 CONCLUSIONS: These results demonstrate that nicotine by itself can stimulate HGF IL-6 and IL-8 production. Nicotine 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 11495082-9 2001 The concentrations of recombinant (r)-IL-8, which covered the levels of activity detected in individual organ cultures or cell cultures of fractionated mucosal cells, could induce chemotactic migration and superoxide anion generation in neutrophils in vitro, and r-GROalpha had synergistic effects on r-IL-8-induced neutrophil activation. Superoxides 206-222 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 11349132-8 2001 P2 antagonists or apyrase, an enzyme which hydrolyzes nucleotides including UDP, inhibit IL-8 production induced by lipopolysaccharide but not by other stimuli. Uridine Diphosphate 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 11349132-5 2001 P2 receptor antagonists or P2Y(6) antisense oligonucleotides inhibit IL-8 release induced by UDP. Oligonucleotides 44-60 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 11349132-9 2001 Furthermore, IL-8 gene expression activated by lipopolysaccharide is enhanced by P2Y(6) overexpression and inhibited by P2Y(6) antisense oligonucleotides. Oligonucleotides 137-153 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 11349132-10 2001 Thus, UDP activates IL-8 production via P2Y(6) in monocytic cells. Uridine Diphosphate 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 11349132-5 2001 P2 receptor antagonists or P2Y(6) antisense oligonucleotides inhibit IL-8 release induced by UDP. Uridine Diphosphate 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 11349132-6 2001 Furthermore, UDP specifically activated IL-8 production in astrocytoma 1321N1 cells transfected with human P2Y(6). Uridine Diphosphate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 11446882-0 2001 Medium-chain fatty acids stimulate interleukin-8 production in Caco-2 cells with different mechanisms from long-chain fatty acids. medium-chain fatty acids 0-24 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 11512674-0 2001 Hyaluronan fragments induce the synthesis of MCP-1 and IL-8 in cultured human peritoneal mesothelial cells. Hyaluronic Acid 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 11512674-2 2001 In this study we investigated the effect of experimentally generated hyaluronan (HA) fragments, degradation products of the extracellular matrix component hyaluronan, which accumulate at inflammatory sites, on the expression of MCP-1 and IL-8 in cultured HMC. Hyaluronic Acid 69-79 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 11512674-2 2001 In this study we investigated the effect of experimentally generated hyaluronan (HA) fragments, degradation products of the extracellular matrix component hyaluronan, which accumulate at inflammatory sites, on the expression of MCP-1 and IL-8 in cultured HMC. Hyaluronic Acid 155-165 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 11428868-5 2001 The induced IL-8 and MCP-1 mRNA and proteins were partially suppressed by U0126, a specific MEK inhibitor, and by SB202190, a selective p38 inhibitor. U 0126 74-79 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 11428868-5 2001 The induced IL-8 and MCP-1 mRNA and proteins were partially suppressed by U0126, a specific MEK inhibitor, and by SB202190, a selective p38 inhibitor. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 11472980-0 2001 Geldanamycin inhibits NF-kappaB activation and interleukin-8 gene expression in cultured human respiratory epithelium. geldanamycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 11472980-3 2001 In the current study, we investigated the effects of geldanamycin on interleukin (IL)-8 gene expression and nuclear factor (NF)-kappaB activation. geldanamycin 53-65 C-X-C motif chemokine ligand 8 Homo sapiens 69-87 11472980-4 2001 Geldanamycin inhibited tumor necrosis factor (TNF)-alpha-mediated IL-8 gene expression in A549 human respiratory epithelial cells as measured by enzyme-linked immunosorbent assay and Northern blot analyses. geldanamycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 11472980-5 2001 In cells transiently transfected with an IL-8 promoter-luciferase reporter plasmid, geldanamycin inhibited TNF-alpha-mediated luciferase activity. geldanamycin 84-96 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 11472980-9 2001 These results demonstrate that geldanamycin inhibits TNF-alpha-mediated IL-8 gene expression in A549 cells by inhibiting activation of the IL-8 promoter. geldanamycin 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 11472980-9 2001 These results demonstrate that geldanamycin inhibits TNF-alpha-mediated IL-8 gene expression in A549 cells by inhibiting activation of the IL-8 promoter. geldanamycin 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 11418672-0 2001 IL-8 production in human lung fibroblasts and epithelial cells activated by the Pseudomonas autoinducer N-3-oxododecanoyl homoserine lactone is transcriptionally regulated by NF-kappa B and activator protein-2. N-(3-oxododecanoyl)homoserine lactone 104-140 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11446882-0 2001 Medium-chain fatty acids stimulate interleukin-8 production in Caco-2 cells with different mechanisms from long-chain fatty acids. long-chain fatty acids 107-129 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 11446882-2 2001 We investigated the effect of fatty acids on interleukin (IL)-8 production in a human intestinal epithelial cell line (Caco-2). Fatty Acids 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 45-63 11798616-10 2001 The levels of IL-8 also increased in HPMC stimulated with TNFalpha(P < 0.01). hydroxypropylmethylcellulose-lactose matrix 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 11478413-7 2001 Tracheal concentrations of IL-8 and MCP-1 were significantly increased in infants who developed BPD (IL-8: P=0.0001; MCP-1: P<0.001, analysis of variance) and correlated with duration of mechanical ventilation and oxygen treatment. Oxygen 217-223 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 11506748-0 2001 Regulation of interleukin-8 expression by nitric oxide in human pancreatic adenocarcinoma. Nitric Oxide 42-54 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 11506748-1 2001 The regulation of interleukin-8 (IL-8) expression by nitric oxide (NO) was determined in human pancreatic cancer cell lines. Nitric Oxide 53-65 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 11506748-1 2001 The regulation of interleukin-8 (IL-8) expression by nitric oxide (NO) was determined in human pancreatic cancer cell lines. Nitric Oxide 53-65 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 11506748-10 2001 Incubation of FG cells with an NO donor, S-nitroso-D,L.-acetyl-penicillamine (SNAP), led to a concentration-dependent and time-dependent induction of IL-8 expression. s-nitroso-d,l.-acetyl-penicillamine 41-76 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 11506748-10 2001 Incubation of FG cells with an NO donor, S-nitroso-D,L.-acetyl-penicillamine (SNAP), led to a concentration-dependent and time-dependent induction of IL-8 expression. snap 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 11798616-11 2001 CONCLUSION: L-PDF inhibited proliferation of HPMC and increased levels of IL-8 and FN in the HPMC. l-pdf 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 11282999-6 2001 Indeed, interleukin 8, a neutrophil chemoattractant, triggered a release of approximately 85% of cellular leukolysins by a process resistant to a mixture of proteinase inhibitors, including aprotinin, BB-94, pepstatin, and E64. batimastat 201-206 C-X-C motif chemokine ligand 8 Homo sapiens 8-21 11297551-7 2001 Consistent with the observed inhibition of NF-kappaB, thalidomide blocked the cytokine-induced expression of NF-kappaB-regulated genes such as those encoding interleukin-8, TRAF1, and c-IAP2. Thalidomide 54-65 C-X-C motif chemokine ligand 8 Homo sapiens 158-171 11282999-6 2001 Indeed, interleukin 8, a neutrophil chemoattractant, triggered a release of approximately 85% of cellular leukolysins by a process resistant to a mixture of proteinase inhibitors, including aprotinin, BB-94, pepstatin, and E64. pepstatin 208-217 C-X-C motif chemokine ligand 8 Homo sapiens 8-21 11282999-6 2001 Indeed, interleukin 8, a neutrophil chemoattractant, triggered a release of approximately 85% of cellular leukolysins by a process resistant to a mixture of proteinase inhibitors, including aprotinin, BB-94, pepstatin, and E64. E 64 223-226 C-X-C motif chemokine ligand 8 Homo sapiens 8-21 11404398-5 2001 A role for ATP in modulating IL-1beta-mediated inflammatory gene expression was supported further by the observation that ATP potentiated the IL-1beta-induced expression of IL-8 mRNA and protein but strongly downregulated IP-10 expression. Adenosine Triphosphate 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 11390455-3 2001 Here we demonstrate that the 15d-PGJ2 can induce IL-8 gene expression. 15-deoxy-delta(12,14)-prostaglandin J2 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 11390455-5 2001 Furthermore, concomitant treatment of monocytes/macrophages with 15d-PGJ2 (2.5 x 10(-6) M) potentiated LPS-induced gene expression of IL-8 mRNA, but suppressed PMA-induction of IL-8 mRNA. 15-deoxy-delta(12,14)-prostaglandin J2 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 11390455-5 2001 Furthermore, concomitant treatment of monocytes/macrophages with 15d-PGJ2 (2.5 x 10(-6) M) potentiated LPS-induced gene expression of IL-8 mRNA, but suppressed PMA-induction of IL-8 mRNA. 15-deoxy-delta(12,14)-prostaglandin J2 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 11390455-6 2001 In addition, treatment of U937 and THP-1 cells with 15d-PGJ2 also resulted in induction of IL-8 gene expression. 15-deoxy-delta(12,14)-prostaglandin J2 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 11390455-7 2001 Further studies demonstrated that 15d-PGJ2 regulated IL-8 gene expression via a ligand-specific and PPARgamma-dependent pathway. 15-deoxy-delta(12,14)-prostaglandin J2 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 11404398-5 2001 A role for ATP in modulating IL-1beta-mediated inflammatory gene expression was supported further by the observation that ATP potentiated the IL-1beta-induced expression of IL-8 mRNA and protein but strongly downregulated IP-10 expression. Adenosine Triphosphate 122-125 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 11426771-6 2001 Interleukin 1beta, interleukin 6, and interleukin 8 levels after cardiopulmonary bypass were significantly (p < 0.05) lower in the colforsin group. Colforsin 134-143 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 11390343-0 2001 Homocysteine induces expression and secretion of monocyte chemoattractant protein-1 and interleukin-8 in human aortic endothelial cells: implications for vascular disease. Homocysteine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 11390343-3 2001 METHODS AND RESULTS: Northern blot and RNase protection assays showed that DL-homocysteine induced mRNA expression of the proinflammatory cytokines monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) in cultured human aortic endothelial cells (HAECs). DL-Homocysteine 75-90 C-X-C motif chemokine ligand 8 Homo sapiens 195-208 11390343-3 2001 METHODS AND RESULTS: Northern blot and RNase protection assays showed that DL-homocysteine induced mRNA expression of the proinflammatory cytokines monocyte chemoattractant protein-1 (MCP-1) and interleukin-8 (IL-8) in cultured human aortic endothelial cells (HAECs). DL-Homocysteine 75-90 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 11390343-7 2001 Homocysteine also triggered the release of MCP-1 and IL-8 protein from HAECs into the culture medium. Homocysteine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 11390343-12 2001 CONCLUSIONS: Pathophysiological levels of L-homocysteine alter endothelial cell function by upregulating MCP-1 and IL-8 expression and secretion. Homocysteine 42-56 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 11350799-9 2001 The concentrations of interleukin-8, granulocyte colony-stimulating factor, monocyte chemoattractant protein-1, and granulocyte-macrophage colony-stimulating factor significantly increased in response to cyclophosphamide. Cyclophosphamide 204-220 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 11399048-0 2001 Nitric oxide suppresses IL-8 transcription by inhibiting c-Jun N-terminal kinase-induced AP-1 activation. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 11415933-9 2001 In contrast, ciglitazone alone had a slight effect on cytokine-induced IL-8 secretion, but markedly inhibited IL-8 secretion from cells pretreated with IL-4. ciglitazone 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 11415933-9 2001 In contrast, ciglitazone alone had a slight effect on cytokine-induced IL-8 secretion, but markedly inhibited IL-8 secretion from cells pretreated with IL-4. ciglitazone 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 11422029-2 2001 OBJECTIVES: To study the effect of dimethylfumarate (DMF) on the production of the chemokines CXCL1, CXCL8, CXCL9, CXCL10 and CXCL11, formerly known as GROalpha, interleukin-8, Mig, IP-10 and IP-9/I-TAC, respectively, in human keratinocytes and peripheral blood mononuclear cells (PBMC). Dimethyl Fumarate 35-51 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 11331079-0 2001 Selective inhibition of interleukin-8-induced neutrophil chemotaxis by ketoprofen isomers. Ketoprofen 71-81 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 11331079-4 2001 Our results show that R- and S-ketoprofen, independently of their potency as PG inhibitors, proved very efficacious in selective inhibition of interleukin-8 (IL-8) chemotaxis. r- and s-ketoprofen 22-41 C-X-C motif chemokine ligand 8 Homo sapiens 143-156 11331079-4 2001 Our results show that R- and S-ketoprofen, independently of their potency as PG inhibitors, proved very efficacious in selective inhibition of interleukin-8 (IL-8) chemotaxis. r- and s-ketoprofen 22-41 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 11331079-5 2001 Inhibition of IL-8 chemotaxis was not restricted to ketoprofen isomer as it could be observed also with drugs belonging to different classes of NSAIDs and it was obtained at drug concentration superimposable to plasma levels after therapeutic administration in patients. Ketoprofen 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 11331079-6 2001 Reduction of IL-8 migration by ketoprofen isomers was paralleled by selective inhibition of PMN response in terms of intracellular calcium concentration ([Ca(2+)]i) increase and extracellular signal regulated kinase(ERK)-2 activation, two intracellular mediators reported to be critical for PMN activities. Ketoprofen 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 11331079-6 2001 Reduction of IL-8 migration by ketoprofen isomers was paralleled by selective inhibition of PMN response in terms of intracellular calcium concentration ([Ca(2+)]i) increase and extracellular signal regulated kinase(ERK)-2 activation, two intracellular mediators reported to be critical for PMN activities. Calcium 131-138 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 11331079-7 2001 It is concluded that inhibition of IL-8 chemotaxis could represent a new clinical target for ketoprofen isomers and, in fact, contribute to the anti-inflammatory activity of NSAIDs. Ketoprofen 93-103 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 11422029-2 2001 OBJECTIVES: To study the effect of dimethylfumarate (DMF) on the production of the chemokines CXCL1, CXCL8, CXCL9, CXCL10 and CXCL11, formerly known as GROalpha, interleukin-8, Mig, IP-10 and IP-9/I-TAC, respectively, in human keratinocytes and peripheral blood mononuclear cells (PBMC). Dimethyl Fumarate 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 101-106 11422029-2 2001 OBJECTIVES: To study the effect of dimethylfumarate (DMF) on the production of the chemokines CXCL1, CXCL8, CXCL9, CXCL10 and CXCL11, formerly known as GROalpha, interleukin-8, Mig, IP-10 and IP-9/I-TAC, respectively, in human keratinocytes and peripheral blood mononuclear cells (PBMC). Dimethyl Fumarate 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 162-175 11422029-6 2001 RESULTS: Northern blot analysis on isolated keratinocyte RNA preparations showed a dose-dependent inhibition of CXCL1, CXCL8, CXCL9, CXCL10 and CXCL11 transcription by DMF. Dimethyl Fumarate 168-171 C-X-C motif chemokine ligand 8 Homo sapiens 119-124 11422029-8 2001 In addition, keratinocytes and PBMC showed in the presence of DMF a dose-dependent inhibition of CXCL8, CXCL9 and CXCL10 protein production. Dimethyl Fumarate 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 97-102 11491146-4 2001 Budesonide (10(-8) M) reduced the amounts of both cytokines (GM-CSF and IL-8) by 40%. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 11491146-0 2001 Effects of formoterol and budesonide on GM-CSF and IL-8 secretion by triggered human bronchial epithelial cells. Budesonide 26-36 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 11491146-2 2001 Addition of formoterol (> or = 10(-10) M) reduced granulocyte macrophage-colony stimulating factor (GM-CSF) levels, as assessed by enzyme-linked immunosorbent assay, by 40-50% and increased interleukin (IL)-8 levels by approximately 50%. Formoterol Fumarate 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 193-211 11491146-9 2001 In conclusion, the combination of budesonide and formoterol reduces the secretion of granulocyte macrophage-colony stimulating factor to basal levels and counteracts the capacity of formoterol alone to induce interleukin-8 production, modulations which may facilitate improved asthma control. Budesonide 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 209-222 11491146-9 2001 In conclusion, the combination of budesonide and formoterol reduces the secretion of granulocyte macrophage-colony stimulating factor to basal levels and counteracts the capacity of formoterol alone to induce interleukin-8 production, modulations which may facilitate improved asthma control. Formoterol Fumarate 49-59 C-X-C motif chemokine ligand 8 Homo sapiens 209-222 11491146-9 2001 In conclusion, the combination of budesonide and formoterol reduces the secretion of granulocyte macrophage-colony stimulating factor to basal levels and counteracts the capacity of formoterol alone to induce interleukin-8 production, modulations which may facilitate improved asthma control. Formoterol Fumarate 182-192 C-X-C motif chemokine ligand 8 Homo sapiens 209-222 11403209-3 2001 We observed that exposure of human aortic smooth muscle cells to pathophysiologically relevant concentrations of homocysteine results in concentration-dependent increases in cytokine-induced MCP-1 and IL-8 secretion. Homocysteine 113-125 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 11403209-4 2001 RNase protection assays revealed that both MCP-1 and IL-8 mRNA concentrations are increased in homocysteine-treated smooth muscle cells when compared to cells activated with cytokines alone. Homocysteine 95-107 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 11403209-6 2001 Cumulatively, these data suggest that homocysteine may increase monocyte recruitment into developing atherosclerotic lesions by upregulating MCP-1 and IL-8 expression in vascular smooth muscle cells. Homocysteine 38-50 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 11404389-0 2001 Priming effects of substance P on calcium changes evoked by interleukin-8 in human neutrophils. Calcium 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 11381075-7 2001 Combined inhibition of MEK by U0126, p38 by SB202190, and Janus kinase (jak) by AG490 revealed that GHSA stimulation of IL-8 production was predominately mediated by MEK and to a lesser extent by p38 pathways, whereas activation of MEK, p38, and jak was required for maximal MCP-1 induction. ghsa 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 11381075-8 2001 Moreover, GHSA-stimulated IL-8 secretion was more sensitive to U0126 (50% inhibitory concentration [IC(50)] = 0.5 microM) than MCP-1 (IC(50) = 10 microM). ghsa 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 11381075-8 2001 Moreover, GHSA-stimulated IL-8 secretion was more sensitive to U0126 (50% inhibitory concentration [IC(50)] = 0.5 microM) than MCP-1 (IC(50) = 10 microM). U 0126 63-68 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 11381075-9 2001 CONCLUSIONS: GHSA stimulates hRPE IL-8 and MCP-1 production through divergent and overlapping, but not identical, intracellular signaling cascades. ghsa 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 11378323-7 2001 We found that 0.5 M NaCl treatment increased mRNA levels of proinflammatory cytokines such as IL-1alpha, IL-6 and IL-8 as well as ICAM-1 in NHEK and IL-1alpha, IL-1beta and IL-6 mRNA levels in NHDF. Sodium Chloride 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 11389120-0 2001 The effect of azithromycin and clarithromycin on ex vivo interleukin-8 (IL-8) release from whole blood and IL-8 production by human alveolar macrophages. Clarithromycin 31-45 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 11389120-1 2001 We investigated the effects of azithromycin and clarithromycin, two antibiotics that possess a broad spectrum of antimicrobial activity (including antimycobacterial activity), on interleukin-8 (IL-8) release from human whole blood leucocytes and lung macrophages. Azithromycin 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 179-192 11389120-1 2001 We investigated the effects of azithromycin and clarithromycin, two antibiotics that possess a broad spectrum of antimicrobial activity (including antimycobacterial activity), on interleukin-8 (IL-8) release from human whole blood leucocytes and lung macrophages. Azithromycin 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 11389120-1 2001 We investigated the effects of azithromycin and clarithromycin, two antibiotics that possess a broad spectrum of antimicrobial activity (including antimycobacterial activity), on interleukin-8 (IL-8) release from human whole blood leucocytes and lung macrophages. Clarithromycin 48-62 C-X-C motif chemokine ligand 8 Homo sapiens 179-192 11389120-1 2001 We investigated the effects of azithromycin and clarithromycin, two antibiotics that possess a broad spectrum of antimicrobial activity (including antimycobacterial activity), on interleukin-8 (IL-8) release from human whole blood leucocytes and lung macrophages. Clarithromycin 48-62 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 11389120-3 2001 Incubation of alveolar macrophages with different concentrations of azithromycin or clarithromycin modified IL-8 production: it increased at a drug concentration of 4 mg/L and decreased at concentration of 400 mg/L. Azithromycin 68-80 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 11389120-3 2001 Incubation of alveolar macrophages with different concentrations of azithromycin or clarithromycin modified IL-8 production: it increased at a drug concentration of 4 mg/L and decreased at concentration of 400 mg/L. Clarithromycin 84-98 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 11389120-4 2001 Our findings suggest that azithromycin and clarithromycin may alter IL-8 production, thus enhancing the clinical effectiveness of these antibiotics. Azithromycin 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 11389120-4 2001 Our findings suggest that azithromycin and clarithromycin may alter IL-8 production, thus enhancing the clinical effectiveness of these antibiotics. Clarithromycin 43-57 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 11440632-7 2001 The antioxidant pyrrolidine dithiocarbamate (PDTC) restored the redox equilibrium by mechanisms that inhibit binding of NF-kappaB to its cognate site on the IL-8 promoter. pyrrolidine dithiocarbamic acid 16-43 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 11440632-7 2001 The antioxidant pyrrolidine dithiocarbamate (PDTC) restored the redox equilibrium by mechanisms that inhibit binding of NF-kappaB to its cognate site on the IL-8 promoter. pyrrolidine dithiocarbamic acid 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 11386618-5 2001 The non-selective NOS inhibitor N-nitro-L-arginine methyl ester (L-NAME) did not affect intracellular ROS levels, but it caused a moderate selective inhibition of IL-8 production. n-nitro-l-arginine methyl ester 32-63 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 11453524-6 2001 Serum levels of IL-6, sIL-6R and IL-8 were markedly elevated in patients with GD before treatment with methimazole (p<0.0001 for IL-6, p<0.006 for sIL-6R, p<0.004 for IL-8) and after 8 weeks of therapy (p<0.011 for IL-6, p<0.04 for IL-8). Methimazole 103-114 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 11386618-5 2001 The non-selective NOS inhibitor N-nitro-L-arginine methyl ester (L-NAME) did not affect intracellular ROS levels, but it caused a moderate selective inhibition of IL-8 production. NG-Nitroarginine Methyl Ester 65-71 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 11325811-9 2001 The IL-17-induced release of IL-6 and IL-8 was concentration-dependently inhibited by SB202190 and by PD98059 in bronchial epithelial cells without affecting cell proliferation or survival. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 102-109 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 12585121-0 2001 [Inhibitory effects of isorhapotigenin on IL-8 production and mRNA expression induced with TNF alpha in normal human synovial cells]. isorhapotigenin 23-38 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 12585121-1 2001 AIM: To study the effects of isorhapotigenin (Iso) on interleukin-8 (IL-8) production and mRNA expression in normal human synovial cells (HSC) induced with TNF alpha. isorhapotigenin 29-44 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 12585121-1 2001 AIM: To study the effects of isorhapotigenin (Iso) on interleukin-8 (IL-8) production and mRNA expression in normal human synovial cells (HSC) induced with TNF alpha. isorhapotigenin 29-44 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 11342615-7 2001 In addition, histamine induces a potent production of IL-6, IL-8, monocyte chemoattractant protein 1, and macrophage-inflammatory protein 1alpha by immature DC and also up-regulates IL-1beta, RANTES, and macrophage-inflammatory protein 1beta but not TNF-alpha and IL-12 mRNA expression. Histamine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 11422128-8 2001 RESULTS: IL-10 inhibited the release of TNF-alpha and of IL-8, but not of IL-5, by activated CBMC. cbmc 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 11359392-8 2001 HgCl2 also stimulated the release of low levels of tumour necrosis factor-alpha and interleukin-8 (but not RANTES), and inhibited the release of interleukin-1alpha by oral keratinocytes. Mercuric Chloride 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 11358991-0 2001 Peroxynitrite mediates cytokine-induced IL-8 gene expression and production by human leukocytes. Peroxynitrous Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 11410418-6 2001 RESULTS: Throughout storage, refrigerated PCs, both ThromboSol-treated and untreated units, displayed a slightly lower level of IL-6 and significantly lower concentration of IL-8 than conventionally stored PCs. thrombosol 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 11437208-2 2001 The objective of the present study was to investigate the fluoride and alkali metal ion release from a relatively simple GIC formulation with fluoride- and alkali metal-free glass and activated with a NaF or KF solution. Fluorides 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 201-204 11358991-5 2001 The addition of ONOO(-) (0.2-80 microM) to whole blood increased nuclear accumulation of AP-1 and NF-kappaB in PMN and mononuclear leukocytes and augmented IL-8 mRNA expression and IL-8 production in a concentration-dependent fashion. onoo(-) 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 11358991-5 2001 The addition of ONOO(-) (0.2-80 microM) to whole blood increased nuclear accumulation of AP-1 and NF-kappaB in PMN and mononuclear leukocytes and augmented IL-8 mRNA expression and IL-8 production in a concentration-dependent fashion. onoo(-) 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 11358991-6 2001 Pyrrolidine dithiocarbamate, an inhibitor of NF-kappaB activation, attenuated approximately 70% of IL-8 release evoked by IL-1beta, TNF-alpha, or ONOO(-). pyrrolidine dithiocarbamic acid 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 11358991-6 2001 Pyrrolidine dithiocarbamate, an inhibitor of NF-kappaB activation, attenuated approximately 70% of IL-8 release evoked by IL-1beta, TNF-alpha, or ONOO(-). onoo 146-150 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 11358991-7 2001 These results indicate that ONOO(-) formation may underlie the action of cytokines towards IL-8 gene expression in human leukocytes. onoo 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 11330965-0 2001 Lysophospholipids increase interleukin-8 expression in ovarian cancer cells. Lysophospholipids 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 11330965-5 2001 Northern blot analysis was used to confirm and examine IL-8 mRNA regulation by lysolipids. lysolipids 79-89 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 11358991-1 2001 Recent studies indicate that nitric oxide (NO) or related compounds may regulate the production of interleukin (IL)-8, a potent proinflammatory chemokine. Nitric Oxide 29-41 C-X-C motif chemokine ligand 8 Homo sapiens 99-117 11358991-2 2001 Here we report that peroxynitrite (ONOO(-)) formed by a reaction of NO with superoxide mediates IL-8 gene expression and IL-8 production in IL-1beta- and TNF-alpha-stimulated human leukocytes in whole blood. Peroxynitrous Acid 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 11358991-2 2001 Here we report that peroxynitrite (ONOO(-)) formed by a reaction of NO with superoxide mediates IL-8 gene expression and IL-8 production in IL-1beta- and TNF-alpha-stimulated human leukocytes in whole blood. Peroxynitrous Acid 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 11358991-2 2001 Here we report that peroxynitrite (ONOO(-)) formed by a reaction of NO with superoxide mediates IL-8 gene expression and IL-8 production in IL-1beta- and TNF-alpha-stimulated human leukocytes in whole blood. onoo 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 11358991-2 2001 Here we report that peroxynitrite (ONOO(-)) formed by a reaction of NO with superoxide mediates IL-8 gene expression and IL-8 production in IL-1beta- and TNF-alpha-stimulated human leukocytes in whole blood. onoo 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 11358991-2 2001 Here we report that peroxynitrite (ONOO(-)) formed by a reaction of NO with superoxide mediates IL-8 gene expression and IL-8 production in IL-1beta- and TNF-alpha-stimulated human leukocytes in whole blood. Superoxides 76-86 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 11358991-2 2001 Here we report that peroxynitrite (ONOO(-)) formed by a reaction of NO with superoxide mediates IL-8 gene expression and IL-8 production in IL-1beta- and TNF-alpha-stimulated human leukocytes in whole blood. Superoxides 76-86 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 11358991-3 2001 The NO synthase inhibitors aminoguanidine and N(G)-nitro-L-arginine methyl ester blocked nuclear accumulation of activator protein-1 (AP-1) and nuclear factor (NF)-kappaB in both polymorphonuclear (PMN) and mononuclear leukocytes and inhibited IL-8 mRNA expression and IL-8 release by approximately 90% in response to IL-1beta and TNF-alpha. pimagedine 27-41 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 11358991-3 2001 The NO synthase inhibitors aminoguanidine and N(G)-nitro-L-arginine methyl ester blocked nuclear accumulation of activator protein-1 (AP-1) and nuclear factor (NF)-kappaB in both polymorphonuclear (PMN) and mononuclear leukocytes and inhibited IL-8 mRNA expression and IL-8 release by approximately 90% in response to IL-1beta and TNF-alpha. pimagedine 27-41 C-X-C motif chemokine ligand 8 Homo sapiens 269-273 11358991-3 2001 The NO synthase inhibitors aminoguanidine and N(G)-nitro-L-arginine methyl ester blocked nuclear accumulation of activator protein-1 (AP-1) and nuclear factor (NF)-kappaB in both polymorphonuclear (PMN) and mononuclear leukocytes and inhibited IL-8 mRNA expression and IL-8 release by approximately 90% in response to IL-1beta and TNF-alpha. NG-Nitroarginine Methyl Ester 46-80 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 11358991-3 2001 The NO synthase inhibitors aminoguanidine and N(G)-nitro-L-arginine methyl ester blocked nuclear accumulation of activator protein-1 (AP-1) and nuclear factor (NF)-kappaB in both polymorphonuclear (PMN) and mononuclear leukocytes and inhibited IL-8 mRNA expression and IL-8 release by approximately 90% in response to IL-1beta and TNF-alpha. NG-Nitroarginine Methyl Ester 46-80 C-X-C motif chemokine ligand 8 Homo sapiens 269-273 11336536-4 2001 The incubation of HCAEC with histamine resulted in low level induction of IL-6 and IL-8 production, which was dose-dependent and attained a plateau at a concentration of 10 microM. Histamine 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 11336536-0 2001 Histamine-induced production of interleukin-6 and interleukin-8 by human coronary artery endothelial cells is enhanced by endotoxin and tumor necrosis factor-alpha. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 11336536-7 2001 In the presence of all stimulatory concentrations of LPS and TNF-alpha tested, histamine was shown to further enhance IL-6 and IL-8 production. Histamine 79-88 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 11336536-10 2001 Since both LPS and TNF-alpha potentiated histamine-induced cytokine production, it is possible that these activators stimulate H-1 receptor expression and/or augment the signal transduction pathways leading to the expression of IL-6 and IL-8. Histamine 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 237-241 11346209-0 2001 Hydrophilic and hydrophobic bile acids exhibit different cytotoxicities through cytolysis, interleukin-8 synthesis and apoptosis in the intestinal epithelial cell lines. Bile Acids and Salts 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 11392584-0 2001 Effect of budesonide and nedocromil sodium on IL-6 and IL-8 release from human nasal mucosa and polyp epithelial cells. Nedocromil 25-42 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 11392584-1 2001 We investigated the effect of budesonide and nedocromil sodium on the secretion of IL-6 and IL-8 by cultured epithelial cells from healthy nasal mucosa and nasal polyps. Nedocromil 45-62 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 11392584-3 2001 Budesonide inhibited FCS-induced IL-6 and IL-8 release in a dose-dependent manner. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 11392584-5 2001 The IC25 of budesonide on IL-8 release was higher in nasal mucosa than in nasal polyps (145 pM vs. 4 pM). Budesonide 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 11392584-6 2001 Nedocromil sodium caused a dose-related inhibitory effect on IL-8 release from nasal mucosa (IC25, 207 nM), while it only had a significant effect in nasal polyps at 10(-5) M. Nedocromil sodium had no effect on IL-6 release. Nedocromil 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 11346209-7 2001 IL-8 synthesis induced by the bile acids was measured using an ELISA assay. Bile Acids and Salts 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11392584-8 2001 Budesonide and nedocromil sodium may exert their anti-inflammatory action in the respiratory mucosa by modulating the secretion of IL-6 and IL-8. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 11392584-8 2001 Budesonide and nedocromil sodium may exert their anti-inflammatory action in the respiratory mucosa by modulating the secretion of IL-6 and IL-8. Nedocromil 15-32 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 11294978-4 2001 Sodium fluoride (NaF) induced apoptosis in both cell types but at different concentrations, with the primary cells being more sensitive to NAF: Proliferation of the type 2 cells and A549 cells was inhibited in the presence of NAF: NaF induced a prolonged activation of MAP kinase ERK. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 11346209-8 2001 RESULTS: The bile acids induced cytotoxic effects, LDH release, IL-8 synthesis and apoptosis, depending on their hydrophobic properties. Bile Acids and Salts 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 11294978-4 2001 Sodium fluoride (NaF) induced apoptosis in both cell types but at different concentrations, with the primary cells being more sensitive to NAF: Proliferation of the type 2 cells and A549 cells was inhibited in the presence of NAF: NaF induced a prolonged activation of MAP kinase ERK. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 11294978-4 2001 Sodium fluoride (NaF) induced apoptosis in both cell types but at different concentrations, with the primary cells being more sensitive to NAF: Proliferation of the type 2 cells and A549 cells was inhibited in the presence of NAF: NaF induced a prolonged activation of MAP kinase ERK. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 226-229 11294978-4 2001 Sodium fluoride (NaF) induced apoptosis in both cell types but at different concentrations, with the primary cells being more sensitive to NAF: Proliferation of the type 2 cells and A549 cells was inhibited in the presence of NAF: NaF induced a prolonged activation of MAP kinase ERK. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 231-234 11392584-9 2001 The different effect of budesonide and nedocromil sodium on IL-6 and IL-8 release may be explained by differences in the mechanisms which regulate the upregulation of these cytokines in inflammatory responses. Budesonide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 11392584-9 2001 The different effect of budesonide and nedocromil sodium on IL-6 and IL-8 release may be explained by differences in the mechanisms which regulate the upregulation of these cytokines in inflammatory responses. Nedocromil 39-56 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 11316662-4 2001 However, BAL macrophages from NA exhibited less suppression of IL-8 and TNF-alpha production by DEX at 4:00 A.M. as compared with 4:00 P.M. (p = 0.0001), whereas in the NNA group DEX suppressed IL-8 and TNF-alpha production equally at both time points. Dexamethasone 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 11306435-0 2001 Benzene-extracted components are important for the major activity of diesel exhaust particles: effect on interleukin-8 gene expression in human bronchial epithelial cells. Benzene 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 11306435-5 2001 Benzene-extracted components showed effects mimicking DEPs on IL-8 gene expression, release of several cytokines (IL-8; granulocyte macrophage colony-stimulating factor; and regulated on activation, normal T cells expressed and secreted) and nuclear factor (NF)-kappa B activation. Benzene 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11306435-5 2001 Benzene-extracted components showed effects mimicking DEPs on IL-8 gene expression, release of several cytokines (IL-8; granulocyte macrophage colony-stimulating factor; and regulated on activation, normal T cells expressed and secreted) and nuclear factor (NF)-kappa B activation. Benzene 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 11298490-8 2001 For example strong calcium responses were seen in neutrophils following stimulation with the CXCR1 and CXCR2 ligands, interleukin (IL-)8, GCP-2 and Gro-beta. Calcium 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 118-136 11290562-9 2001 Pretreatment of HPFBs with actinomycin D or puromycin dose-dependently reduced cytokine-stimulated IL-8 and MCP-1 secretion, which suggested de novo chemokine synthesis. hpfbs 16-21 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 11290562-9 2001 Pretreatment of HPFBs with actinomycin D or puromycin dose-dependently reduced cytokine-stimulated IL-8 and MCP-1 secretion, which suggested de novo chemokine synthesis. Dactinomycin 27-40 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 11290562-9 2001 Pretreatment of HPFBs with actinomycin D or puromycin dose-dependently reduced cytokine-stimulated IL-8 and MCP-1 secretion, which suggested de novo chemokine synthesis. Puromycin 44-53 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 11306458-3 2001 The results also show short-term exposure of MCF-7 cells to either Adriamycin or FUdR rapidly increases, in a dose-dependent manner, the release of the angiogenic cytokine, interleukin-8(IL-8), which is released at consistently higher levels in metastatic cell lines. Doxorubicin 67-77 C-X-C motif chemokine ligand 8 Homo sapiens 173-186 11306458-3 2001 The results also show short-term exposure of MCF-7 cells to either Adriamycin or FUdR rapidly increases, in a dose-dependent manner, the release of the angiogenic cytokine, interleukin-8(IL-8), which is released at consistently higher levels in metastatic cell lines. Doxorubicin 67-77 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 11306458-5 2001 Survivors of sequential treatment with Adriamycin and FUdR (MCF-7 A/F) release the most IL-8 and express the greatest phenotypic variance from the parental, MCF-7 cells. Doxorubicin 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 11309322-13 2001 CONCLUSIONS: Addition of TNF to melphalan during IHP results in significant differences in post-IHP production of IL-6 and IL-8 with associated changes in mean arterial blood pressure and greater regional toxicity, as reflected in higher levels of serum bilirubin. Melphalan 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 11296168-11 2001 FENO may be related to neutrophilic inflammation driven by the chemoattractant IL-8. flubendiamide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 11254557-7 2001 Anti-CD14 monoclonal antibody (MAb) MY4, anti-TLR4 MAb HTA125, and the synthetic lipid A precursor LA-14-PP almost completely inhibited the IL-8-inducing activities of LTA as well as LPS on OCT-treated THP-1 cells, but these treatments increased MDP activity. la-14-pp 99-107 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 11359455-0 2001 The IL-8 release from cultured human keratinocytes, mediated by antibodies to bullous pemphigoid autoantigen 180, is inhibited by dapsone. Dapsone 130-137 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 11359455-7 2001 We demonstrate that dapsone, but not nicotinamide, in its pharmacological range, inhibits the IL-8, but not the IL-6 release from NHEK, induced by anti-BP180 IgG, in a dose-dependent fashion as detected by ELISA. Dapsone 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 11359455-8 2001 IL-8 mRNA levels, as determined by RT-PCR, were the same in cells treated with BP IgG alone compared to cells treated with BP IgG plus dapsone. Dapsone 135-142 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11359455-9 2001 This observation suggests that dapsone inhibits the BP IgG-induced IL-8 release from cultured NHEK by mechanisms at the post-transcriptional level. Dapsone 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 11399518-10 2001 Production of inflammatory cytokines (IL-1 beta, TNF-alpha, IL-6, IL-8) was significantly increased, mostly by the Sambucol Black Elderberry Extract (2-45 fold), as compared to LPS, a known monocyte activator (3.6-10.7 fold). sambucol black elderberry 115-140 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 11321363-1 2001 Interleukin-8 (IL-8), C5a and N-formyl-methionyl-leucyl-phenylalanine (fMLP) are chemotactic peptides with predominant effects on leukocytes during inflammation. N-Formylmethionine Leucyl-Phenylalanine 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 11392610-0 2001 Calcium-dependent interleukin-8 gene expression in T84 human colonic epithelial cells. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 11392610-7 2001 RESULTS: A23187 and thapsigargin caused a dose- and time-dependent accumulation of IL-8 mRNA and protein production which was dependent on the release of Ca2+ from intracellular stores. Calcimycin 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 11328384-1 2001 Although adenosine/uridine (AU)-rich sequences in the 3"-untranslated region (UTR) of the interleukin-8 (IL-8) gene have been suggested to contribute to its post-transcriptional regulation, the molecular basis whereby this occurs still needs to be understood. Adenosine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 11295678-2 2001 In vitro studies have shown that desloratadine inhibits the release or generation of multiple inflammatory mediators, including IL-4, IL-6, IL-8, IL-13, PGD(2), leukotriene C(4), tryptase, histamine, and the TNF-alpha-induced chemokine RANTES. desloratadine 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 11328384-1 2001 Although adenosine/uridine (AU)-rich sequences in the 3"-untranslated region (UTR) of the interleukin-8 (IL-8) gene have been suggested to contribute to its post-transcriptional regulation, the molecular basis whereby this occurs still needs to be understood. Adenosine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 11328384-1 2001 Although adenosine/uridine (AU)-rich sequences in the 3"-untranslated region (UTR) of the interleukin-8 (IL-8) gene have been suggested to contribute to its post-transcriptional regulation, the molecular basis whereby this occurs still needs to be understood. Uridine 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 11328384-1 2001 Although adenosine/uridine (AU)-rich sequences in the 3"-untranslated region (UTR) of the interleukin-8 (IL-8) gene have been suggested to contribute to its post-transcriptional regulation, the molecular basis whereby this occurs still needs to be understood. Uridine 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 11328384-1 2001 Although adenosine/uridine (AU)-rich sequences in the 3"-untranslated region (UTR) of the interleukin-8 (IL-8) gene have been suggested to contribute to its post-transcriptional regulation, the molecular basis whereby this occurs still needs to be understood. Gold 28-30 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 11328384-1 2001 Although adenosine/uridine (AU)-rich sequences in the 3"-untranslated region (UTR) of the interleukin-8 (IL-8) gene have been suggested to contribute to its post-transcriptional regulation, the molecular basis whereby this occurs still needs to be understood. Gold 28-30 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 11392610-7 2001 RESULTS: A23187 and thapsigargin caused a dose- and time-dependent accumulation of IL-8 mRNA and protein production which was dependent on the release of Ca2+ from intracellular stores. Thapsigargin 20-32 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 11392610-8 2001 FK506, a specific inhibitor of calcineurin, inhibited A23187- and thapsigargin-induced IL-8 mRNA expression in a dose dependent manner. Tacrolimus 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 11392610-8 2001 FK506, a specific inhibitor of calcineurin, inhibited A23187- and thapsigargin-induced IL-8 mRNA expression in a dose dependent manner. Calcimycin 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 11392610-8 2001 FK506, a specific inhibitor of calcineurin, inhibited A23187- and thapsigargin-induced IL-8 mRNA expression in a dose dependent manner. Thapsigargin 66-78 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 11392610-9 2001 Reporter gene studies and actinomycin D chase experiments showed that A23187 and thapsigargin enhanced IL-8 gene transcription and stabilized IL-8 mRNA transcripts, respectively. Calcimycin 70-76 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 11392610-9 2001 Reporter gene studies and actinomycin D chase experiments showed that A23187 and thapsigargin enhanced IL-8 gene transcription and stabilized IL-8 mRNA transcripts, respectively. Calcimycin 70-76 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 11392610-9 2001 Reporter gene studies and actinomycin D chase experiments showed that A23187 and thapsigargin enhanced IL-8 gene transcription and stabilized IL-8 mRNA transcripts, respectively. Thapsigargin 81-93 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 11392610-9 2001 Reporter gene studies and actinomycin D chase experiments showed that A23187 and thapsigargin enhanced IL-8 gene transcription and stabilized IL-8 mRNA transcripts, respectively. Thapsigargin 81-93 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 11254300-2 2001 The kinetic effects of added salts (NaF, NaCl, NaBr, and NaNO(3)) on the reaction rate in SB3-14 aqueous micellar solutions have also been studied. 3-(N,N-Dimethylmyristylammonio)propanesulfonate 90-96 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 11240858-5 2001 The IL-8 production activity of polysaccharide from P. gingivalis was higher than that of other cell-surface components. Polysaccharides 32-46 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 11347983-8 2001 IL-8 and IL-10 levels were significantly higher in the CPB than in the off-pump patients after reperfusion (p=0.006 and 0.001 respectively). cpb 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11441488-0 2001 Effects of polysiloxane coating of NaF on the release profile of fluoride ion from Bis-GMA/TEGDMA resin containing NaF. Fluorides 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 11280799-10 2001 Additional transfection studies with progressively COOH-terminally truncated PTHrP1-87 defined a 23-amino acid sequence, PTHrP65-87, required for PTHrP1-87 to robustly stimulate IL-8 in prostate cancer cells. Carbonic Acid 51-55 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 11441488-3 2001 Bis-GMA/TEGDMA resin containing NaF powder treated with AMMS released lower concentrations of fluoride for longer periods when compared with that containing untreated NaF. Fluorides 94-102 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 11260138-8 2001 Full interleukin 8 induction required hexa-acylated lipid A and was decreased by between 50% and 70% in the presence of O-antigen. Lipid A 52-59 C-X-C motif chemokine ligand 8 Homo sapiens 5-18 11441488-4 2001 However, AMMS treatment of NaF was less effective for the regulation of fluoride released from the resin than gamma-methacryloxypropyltrimethoxysilane (gamma-MPTS) treatment, despite its higher hydrophobic polysiloxane layer formation. Fluorides 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 11441488-0 2001 Effects of polysiloxane coating of NaF on the release profile of fluoride ion from Bis-GMA/TEGDMA resin containing NaF. Fluorides 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 11441488-0 2001 Effects of polysiloxane coating of NaF on the release profile of fluoride ion from Bis-GMA/TEGDMA resin containing NaF. Bisphenol A-Glycidyl Methacrylate 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 11441488-6 2001 The present findings suggested, therefore, that alkoxysilane should be chosen based not only on hydrophobicity but also the density of polysiloxane to effectively regulate fluoride release from the restorative resin containing NaF. alkoxysilane 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 227-230 11441488-0 2001 Effects of polysiloxane coating of NaF on the release profile of fluoride ion from Bis-GMA/TEGDMA resin containing NaF. Bisphenol A-Glycidyl Methacrylate 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 11441488-6 2001 The present findings suggested, therefore, that alkoxysilane should be chosen based not only on hydrophobicity but also the density of polysiloxane to effectively regulate fluoride release from the restorative resin containing NaF. Fluorides 172-180 C-X-C motif chemokine ligand 8 Homo sapiens 227-230 11441488-1 2001 The aim of this study was to regulate fluoride release from restorative resin containing NaF using N-(beta-aminoethyl)-gamma-aminopropylmethyldimethoxysilane (AMMS) and evaluate factors that regulate fluoride release from the resin. Fluorides 38-46 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 11441488-1 2001 The aim of this study was to regulate fluoride release from restorative resin containing NaF using N-(beta-aminoethyl)-gamma-aminopropylmethyldimethoxysilane (AMMS) and evaluate factors that regulate fluoride release from the resin. n-(beta-aminoethyl)-gamma-aminopropylmethyldimethoxysilane 99-157 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 11441488-2 2001 ESCA analysis, FT-IR measurements along with SEM observations demonstrated that a polysiloxane layer was formed on the surface of NaF treated with AMMS. Siloxanes 82-94 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 11441488-3 2001 Bis-GMA/TEGDMA resin containing NaF powder treated with AMMS released lower concentrations of fluoride for longer periods when compared with that containing untreated NaF. Bisphenol A-Glycidyl Methacrylate 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 11441488-3 2001 Bis-GMA/TEGDMA resin containing NaF powder treated with AMMS released lower concentrations of fluoride for longer periods when compared with that containing untreated NaF. Bisphenol A-Glycidyl Methacrylate 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 11441488-3 2001 Bis-GMA/TEGDMA resin containing NaF powder treated with AMMS released lower concentrations of fluoride for longer periods when compared with that containing untreated NaF. triethylene glycol dimethacrylate 8-14 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 11231943-5 2001 Butyrate maximally stimulated cell cycle arrest, apoptosis, alkaline phosphatase activity, transepithelial resistance, cell migration, urokinase receptor expression, and interleukin 8 secretion in undifferentiated Caco-2 cells, whereas differentiated Caco-2 cells were essentially resistant to these effects. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 170-183 11222496-9 2001 By blocking activation of ERK1/2 with a MEK-specific inhibitor, PD98059, CD40-dependent secretion of the pro-inflammatory cytokines, TNF-alpha, IL-6 and IL-8, was demonstrated to be linked to the ERK1/2 pathway. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 64-71 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 11230738-6 2001 Degranulation induced by 100 to 500 micromol/L TCDCA was an active and regulated release because it was completely abolished by a tyrosine kinase inhibitor (genistein), by a microfilament inhibitor (cytochalasin B), and by incubation at 4 degrees C. Furthermore, eosinophils stimulated with 10 to 250 micromol/L TCDCA vigorously produced superoxide and interleukin-8 (IL-8). Taurochenodeoxycholic Acid 47-52 C-X-C motif chemokine ligand 8 Homo sapiens 353-366 11230738-6 2001 Degranulation induced by 100 to 500 micromol/L TCDCA was an active and regulated release because it was completely abolished by a tyrosine kinase inhibitor (genistein), by a microfilament inhibitor (cytochalasin B), and by incubation at 4 degrees C. Furthermore, eosinophils stimulated with 10 to 250 micromol/L TCDCA vigorously produced superoxide and interleukin-8 (IL-8). Taurochenodeoxycholic Acid 47-52 C-X-C motif chemokine ligand 8 Homo sapiens 368-372 11230738-6 2001 Degranulation induced by 100 to 500 micromol/L TCDCA was an active and regulated release because it was completely abolished by a tyrosine kinase inhibitor (genistein), by a microfilament inhibitor (cytochalasin B), and by incubation at 4 degrees C. Furthermore, eosinophils stimulated with 10 to 250 micromol/L TCDCA vigorously produced superoxide and interleukin-8 (IL-8). Genistein 157-166 C-X-C motif chemokine ligand 8 Homo sapiens 353-366 11230738-6 2001 Degranulation induced by 100 to 500 micromol/L TCDCA was an active and regulated release because it was completely abolished by a tyrosine kinase inhibitor (genistein), by a microfilament inhibitor (cytochalasin B), and by incubation at 4 degrees C. Furthermore, eosinophils stimulated with 10 to 250 micromol/L TCDCA vigorously produced superoxide and interleukin-8 (IL-8). Genistein 157-166 C-X-C motif chemokine ligand 8 Homo sapiens 368-372 11159726-7 2001 The maximum extent of attenuation was RANTES > or = eotaxin > GM-CSF >> IL-8, and was prevented by either propranolol (1 microM), a non-selective beta-adrenoceptor antagonist, or ICI 118511 (IC(50) 15 nM), a selective beta(2)-adrenoceptor antagonist. Propranolol 118-129 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 11238519-5 2001 Dexamethasone (50 nM) decreased IL-8 production from adipose tissue fragments by 57% (P < 0.01) and from adipocytes by 37% (P < 0.05). Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 11238519-7 2001 Thus, the effect of proinflammatory cytokines and dexamethasone on IL-8 production in adipose tissue seems to be mediated at the transcriptional level. Dexamethasone 50-63 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 11261782-8 2001 Increased ICAM-3 expression was of functional significance, such that processes stimulated or co-stimulated via ICAM-3 (homotypic aggregation, IL-8 secretion) were clearly enhanced upon RA pretreatment, suggesting that RA may contribute via hitherto unrecognized pathways to immune function and host defense. Tretinoin 186-188 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 11354255-3 2001 Recent studies have revealed that cells possess two cholesterol-sensors: (a) Receptor-Ck which senses the extracellular cholesterol and initiates signalling pathway responsible for the regulation of genes involved in the cell cycle, cell death, cellular cholesterol homeostasis and cytokines including IL-6; (b) LxR alpha which senses intracellular oxysterols and controls genes involved in cell death, cellular cholesterol homeostasis and cytokine IL-8. Cholesterol 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 449-453 11354255-4 2001 These cholesterol sensors define the molecular mechanism responsible for cholesterol-depended regulation of cellular synthesis and secretion of cytokines (IL-6, IL-8) within arterial wall. Cholesterol 6-17 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 11354255-4 2001 These cholesterol sensors define the molecular mechanism responsible for cholesterol-depended regulation of cellular synthesis and secretion of cytokines (IL-6, IL-8) within arterial wall. Cholesterol 73-84 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 11159540-8 2001 Mechanisms of intracellular signaling differed; the deactivation of IL-8-induced chemotaxis resulted from tyrphostin-sensitive interactions of AT III-signaling with the IL-8 signal transduction pathway, whereas AT III-induced chemotaxis involved protein kinase C and phosphodiesterases. Tyrphostins 106-116 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 11159540-8 2001 Mechanisms of intracellular signaling differed; the deactivation of IL-8-induced chemotaxis resulted from tyrphostin-sensitive interactions of AT III-signaling with the IL-8 signal transduction pathway, whereas AT III-induced chemotaxis involved protein kinase C and phosphodiesterases. Tyrphostins 106-116 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 11354255-3 2001 Recent studies have revealed that cells possess two cholesterol-sensors: (a) Receptor-Ck which senses the extracellular cholesterol and initiates signalling pathway responsible for the regulation of genes involved in the cell cycle, cell death, cellular cholesterol homeostasis and cytokines including IL-6; (b) LxR alpha which senses intracellular oxysterols and controls genes involved in cell death, cellular cholesterol homeostasis and cytokine IL-8. Cholesterol 52-63 C-X-C motif chemokine ligand 8 Homo sapiens 449-453 11354255-3 2001 Recent studies have revealed that cells possess two cholesterol-sensors: (a) Receptor-Ck which senses the extracellular cholesterol and initiates signalling pathway responsible for the regulation of genes involved in the cell cycle, cell death, cellular cholesterol homeostasis and cytokines including IL-6; (b) LxR alpha which senses intracellular oxysterols and controls genes involved in cell death, cellular cholesterol homeostasis and cytokine IL-8. Cholesterol 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 449-453 11354255-3 2001 Recent studies have revealed that cells possess two cholesterol-sensors: (a) Receptor-Ck which senses the extracellular cholesterol and initiates signalling pathway responsible for the regulation of genes involved in the cell cycle, cell death, cellular cholesterol homeostasis and cytokines including IL-6; (b) LxR alpha which senses intracellular oxysterols and controls genes involved in cell death, cellular cholesterol homeostasis and cytokine IL-8. Cholesterol 120-131 C-X-C motif chemokine ligand 8 Homo sapiens 449-453 11161457-6 2001 RESULTS: glutamine given in vivo and in vitro significantly decreased IL-6 [1.4 (0.8-8.5) vs 8.9 (1.0-43.9)] and IL-8 production [5.8 (0-51.4) vs. 53.0 (2.5-114.6), pg/mg wet tissue], median (range), both P< or =0.01, in comparison to no glutamine experiments. Glutamine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 11159726-14 2001 We conclude in human ASM cells that activation of beta(2)-adrenoceptors and generation of cyclic AMP is negatively-linked to the release, elicited by IL-1 beta or TNF alpha, of eosinophil-activating cytokines such as GM-CSF, RANTES and eotaxin, but not IL-8. Cyclic AMP 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 253-257 11277180-10 2001 Higher IL-6 and IL-8 levels were directly associated with lower phosphorus levels. Phosphorus 64-74 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 11234901-7 2001 Basal and tumor necrosis factor-alpha-inducible phosphorylation of ERK1/2 and secretion of IL-8 and VEGF could be specifically inhibited by a MEK inhibitor, U0126. U 0126 157-162 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 11174195-2 2001 OBJECTIVE: We aimed to investigate the effects of O3 and NO2 on the release of IL-8, GM-CSF, RANTES, and soluble intercellular adhesion molecule 1 (sICAM-1) from human bronchial epithelial cells (HBECs) of nonatopic nonasthmatic subjects (nonasthmatic subjects) and atopic subjects with mild asthma (asthmatic subjects) in vitro. Ozone 50-52 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 11174195-2 2001 OBJECTIVE: We aimed to investigate the effects of O3 and NO2 on the release of IL-8, GM-CSF, RANTES, and soluble intercellular adhesion molecule 1 (sICAM-1) from human bronchial epithelial cells (HBECs) of nonatopic nonasthmatic subjects (nonasthmatic subjects) and atopic subjects with mild asthma (asthmatic subjects) in vitro. Nitrogen Dioxide 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 11174195-6 2001 Exposure of HBECs of asthmatic subjects to both 50 to 100 ppb O3 and 200 to 400 ppb NO2 significantly increased the release of IL-8, GM-CSF, RANTES, and sICAM-1 from these cells after 24 hours of incubation. Nitrogen Dioxide 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 11174198-3 2001 OBJECTIVE: The objective of this study was to examine whether histamine can alter the expression of the 4 genes encoding H1 receptor, IL-8, TNF-alpha, and ZO-1 tight-junction protein in cultured nasal epithelial cells. Histamine 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 121-138 11174198-6 2001 RESULTS: Histamine significantly upregulated IL-8 mRNA expression and significantly downregulated ZO-1 mRNA expression. Histamine 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 11251624-6 2001 On separate occasions, we investigated the effect of PTL11028, a highly potent and selective Der p1 inhibitor, on HDM allergen-induced release of IL-8, following activation of HDM allergen by incubation with cysteine. PTL 11028 53-61 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 11251624-11 2001 Incubation with HDM allergen led to a significant, dose and time-dependent increase in the release of IL-8, which was further enhanced when the allergen extract was pre-activated with cysteine. Cysteine 184-192 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 11251624-13 2001 Prepared solutions of various concentrations of IL-8, IL-1beta and sICAM-1 exposed to cigarette smoke demonstrated a dramatic exposure time-dependent decrease in the detectable amount of these mediators, an effect which was abrogated by GSH. Glutathione 237-240 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 11159885-0 2001 Disaccharides derived from heparin or heparan sulfate regulate IL-8 and IL-1 beta secretion by intestinal epithelial cells. Disaccharides 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 11159885-0 2001 Disaccharides derived from heparin or heparan sulfate regulate IL-8 and IL-1 beta secretion by intestinal epithelial cells. Heparin 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 11159885-0 2001 Disaccharides derived from heparin or heparan sulfate regulate IL-8 and IL-1 beta secretion by intestinal epithelial cells. Heparitin Sulfate 38-53 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 11289656-8 2001 Dexamethasone also inhibited the release of IL-6, IL-8, and PGE2 induced by IL-1beta in both OA and RA fibroblasts. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 11289656-10 2001 Hymenialdisine inhibited IL-6 production and reduced IL-8 production dependent on synovial cell strains. hymenialdisine 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 11216967-8 2001 4) Monocyte chemoattractant protein-1 enhanced the generation of O2- in monocytes from unstable angina patients, and the antioxidant glutathione-monoethyl ester suppressed the production of IL-8 and MCP-1 in these cells. S-ethyl glutathione 133-160 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 11251036-6 2001 The infusion of hydrocortisone was associated with significant reductions in serum IL-6 and IL-8 levels and with earlier resolution of the sepsis-induced organ dysfunction syndrome. Hydrocortisone 16-30 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 11160671-12 2001 Finally, we demonstrate that the presence of the proteasome inhibitor MG-132 inhibits the induction of NF-kappa B binding, as well as IL-8 expression, supporting the role of NF-kappa B. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 70-76 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 11344824-9 2001 Acetaldehyde markedly increased TNF-alpha and IL-8 expression, stimulated IL-1 beta and IL-8 secretion, increased lipid peroxidation damage and decreased catalase activity, while LPS exposure induced the expression of TNF-alpha, TGF-beta 1, IL-6 and IL-8, the secretion of TGF-beta 1, IL-1 beta, IL-6 and IL-8, and a decrease in catalase activity. Acetaldehyde 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 11344824-9 2001 Acetaldehyde markedly increased TNF-alpha and IL-8 expression, stimulated IL-1 beta and IL-8 secretion, increased lipid peroxidation damage and decreased catalase activity, while LPS exposure induced the expression of TNF-alpha, TGF-beta 1, IL-6 and IL-8, the secretion of TGF-beta 1, IL-1 beta, IL-6 and IL-8, and a decrease in catalase activity. Acetaldehyde 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 11344824-9 2001 Acetaldehyde markedly increased TNF-alpha and IL-8 expression, stimulated IL-1 beta and IL-8 secretion, increased lipid peroxidation damage and decreased catalase activity, while LPS exposure induced the expression of TNF-alpha, TGF-beta 1, IL-6 and IL-8, the secretion of TGF-beta 1, IL-1 beta, IL-6 and IL-8, and a decrease in catalase activity. Acetaldehyde 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 11344824-9 2001 Acetaldehyde markedly increased TNF-alpha and IL-8 expression, stimulated IL-1 beta and IL-8 secretion, increased lipid peroxidation damage and decreased catalase activity, while LPS exposure induced the expression of TNF-alpha, TGF-beta 1, IL-6 and IL-8, the secretion of TGF-beta 1, IL-1 beta, IL-6 and IL-8, and a decrease in catalase activity. Acetaldehyde 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 11166656-11 2001 In contrast, after ex vivo priming with TNFalpha or IL-8, neutrophils showed a decreased H2O2 production in response to bacterial N-formyl peptides. Hydrogen Peroxide 89-93 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 11166656-11 2001 In contrast, after ex vivo priming with TNFalpha or IL-8, neutrophils showed a decreased H2O2 production in response to bacterial N-formyl peptides. n-formyl peptides 130-147 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 11180086-0 2001 Interleukin-8 serum level shift in patients with ovarian carcinoma undergoing paclitaxel-containing chemotherapy. Paclitaxel 78-88 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 11158523-1 2001 Polymorphonuclear leukocytes (PMN) of the newborn, to a greater extent than those of the adult, have the ability to amplify PMN recruitment to an inflammatory site by their own release of IL-8, and this process is inhibited by dexamethasone. Dexamethasone 227-240 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 11439889-0 2001 [Calcium dependent effect of clarithromycin on IL-8 production in cultured human epidermal cells]. Calcium 1-8 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 11439889-0 2001 [Calcium dependent effect of clarithromycin on IL-8 production in cultured human epidermal cells]. Clarithromycin 29-43 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 11180086-1 2001 BACKGROUND: Paclitaxel has been described to induce interleukin-8 (IL-8) transcription and secretion in human ovarian carcinoma cells. Paclitaxel 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 11180086-1 2001 BACKGROUND: Paclitaxel has been described to induce interleukin-8 (IL-8) transcription and secretion in human ovarian carcinoma cells. Paclitaxel 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 11180086-2 2001 The objective of this study was to investigate possible clinical implications of the effect of paclitaxel on IL-8 serum levels in patients suffering from ovarian carcinoma. Paclitaxel 95-105 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 11180086-12 2001 CONCLUSIONS: The authors found a significant decrease in IL-8 serum levels in patients undergoing a paclitaxel-containing chemotherapy regimen, indicating that IL-8 possibly acts as a useful monitoring marker in patients with ovarian carcinoma. Paclitaxel 100-110 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 11180086-12 2001 CONCLUSIONS: The authors found a significant decrease in IL-8 serum levels in patients undergoing a paclitaxel-containing chemotherapy regimen, indicating that IL-8 possibly acts as a useful monitoring marker in patients with ovarian carcinoma. Paclitaxel 100-110 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 11270500-8 2001 Several studies have shown macrolides to inhibit interleukin gene expression for IL-6 and IL-8 and also to inhibit the expression of intercellular adhesion molecule essential for the recruitment of inflammatory cells. Macrolides 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 11145710-4 2001 Cytochalasin D significantly inhibited the recycling of both CXCR1 and CXCR2 following IL-8-induced internalization, the inhibition being more pronounced for CXCR2 than for CXCR1. Cytochalasin D 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 11133489-4 2001 A high dose of ASA blocked IL-1 beta- and TNF-alpha-induced TNF-alpha and IL-8 expression, respectively. Aspirin 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 11121390-7 2001 Finally, using the specific MAPK inhibitor PD-98059, we demonstrated that MAPK activation is needed for neutrophil chemotaxis toward interleukin-8 and its priming by GM-CSF. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 11774557-0 2001 Effect of polysaccharide sulfates on the production of interleukin-8 in an ex vivo model. polysaccharide sulfates 10-33 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 12083969-8 2001 Repair of both defective channels and high IL-8 secretion can also be effected by treatment with the candidate CF drug CPX, which is in clinical trials in CF patients. 1,3-dipropyl-8-cyclopentylxanthine 119-122 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 11133500-0 2001 Mechanism of dexamethasone-mediated interleukin-8 gene suppression in cultured airway epithelial cells. Dexamethasone 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 36-49 11133500-1 2001 The effects of dexamethasone, a glucocorticoid analog, on interleukin 8 (IL-8) gene expression were studied in cultures of primary human tracheobronchial epithelial cells and an immortalized human bronchial epithelial cell line, HBE1 cells. Dexamethasone 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 11133500-1 2001 The effects of dexamethasone, a glucocorticoid analog, on interleukin 8 (IL-8) gene expression were studied in cultures of primary human tracheobronchial epithelial cells and an immortalized human bronchial epithelial cell line, HBE1 cells. Dexamethasone 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 11133500-2 2001 Dexamethasone inhibited IL-8 mRNA and protein expression in a concentration- and time-dependent manner. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 11133500-4 2001 Instead, there was a change in IL-8 mRNA stability in dexamethasone-treated cultures. Dexamethasone 54-67 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 11133500-5 2001 Under actinomycin D treatment, IL-8 mRNA was quite stable in dexamethasone-depleted cultures, while in dexamethasone-pretreated cultures, IL-8 message was rapidly degraded within the first hour, then leveled off. Dactinomycin 6-19 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 11133500-5 2001 Under actinomycin D treatment, IL-8 mRNA was quite stable in dexamethasone-depleted cultures, while in dexamethasone-pretreated cultures, IL-8 message was rapidly degraded within the first hour, then leveled off. Dexamethasone 61-74 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 12083969-10 2001 CPX also suppresses the synthesis and secretion of IL-8 from CF epithelial cells, presumably by virtue of its repair of the trafficking defect of mutant CFTR. 1,3-dipropyl-8-cyclopentylxanthine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 11133500-5 2001 Under actinomycin D treatment, IL-8 mRNA was quite stable in dexamethasone-depleted cultures, while in dexamethasone-pretreated cultures, IL-8 message was rapidly degraded within the first hour, then leveled off. Dexamethasone 103-116 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 11133500-6 2001 When dexamethasone and actinomycin D were added simultaneously to dexamethasone-depleted cultures, IL-8 mRNA remained rather stable. Dexamethasone 5-18 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 11167428-7 2001 Both agents caused significant decreases in IL-8 levels (propofol: 30%, midazolam: 48%, p < 0.05). Propofol 57-65 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 12083969-15 2001 For the latter algorithm we modified IL-8 secretion from CF cells by treatment with wild-type CFTR, with CPX, or by exposure to bacteria. 1,3-dipropyl-8-cyclopentylxanthine 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 11167428-7 2001 Both agents caused significant decreases in IL-8 levels (propofol: 30%, midazolam: 48%, p < 0.05). Midazolam 72-81 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 11133500-6 2001 When dexamethasone and actinomycin D were added simultaneously to dexamethasone-depleted cultures, IL-8 mRNA remained rather stable. Dactinomycin 23-36 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 11133500-6 2001 When dexamethasone and actinomycin D were added simultaneously to dexamethasone-depleted cultures, IL-8 mRNA remained rather stable. Dexamethasone 66-79 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 11167428-9 2001 In conclusion, during 48 h of continuous infusion, propofol stimulated, while midazolam suppressed, the production of the pro-inflammatory cytokines IL-1beta, IL-6 and TNF-alpha, and both caused suppression of IL-8 production. Propofol 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 11673649-3 2001 High glucose concentrations increased IL-8 mRNA levels in a MAPK-p38-dependent manner, which was suppressed by shear stress. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 11133500-8 2001 These results suggest that a posttranscriptional mechanism, which requires dexamethasone-dependent new protein synthesis, is involved in the regulation of IL-8 mRNA by dexamethasone in airway epithelial cells. Dexamethasone 75-88 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 11133500-8 2001 These results suggest that a posttranscriptional mechanism, which requires dexamethasone-dependent new protein synthesis, is involved in the regulation of IL-8 mRNA by dexamethasone in airway epithelial cells. Dexamethasone 168-181 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 11673649-4 2001 Measurement of IL-8 protein in HUVEC culture media by ELISA demonstrated that IL-8 secretion was also increased by high glucose and suppressed by shear stress. Glucose 120-127 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 11673649-4 2001 Measurement of IL-8 protein in HUVEC culture media by ELISA demonstrated that IL-8 secretion was also increased by high glucose and suppressed by shear stress. Glucose 120-127 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 11156247-7 2000 Treatment with paclitaxel and C225 down-regulated the expression of basic fibroblast growth factor, vascular endothelial cell growth factor, interleukin-8, and matrix metalloproteinase type 9 and inhibited tumor-induced neovascularity compared with untreated controls (P < 0.005). Paclitaxel 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 141-154 11455057-5 2001 The animals were divided in 2 groups of 10 each: (1) intravenous injection of sodium fluorescein (14 mg/kg of body weight)--Group NaF, (2) controls (injection of NaCl 0.9%)--Group CTRL. Fluorescein 78-96 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 11235021-2 2001 Since interleukin-8 and interleukin-10 are involved in the pathogenesis of psoriasis, the aim of our study was to investigate the effect of dithranol on interleukin-8, interleukin-10 mRNA production and interleukin-10 receptor expression of the HaCaT keratinocyte cell line which is commonly used in experiments examining the effects of therapeutic drugs on keratinocytes. Anthralin 140-149 C-X-C motif chemokine ligand 8 Homo sapiens 153-166 12094614-0 2001 Green tea catechins and vitamin E inhibit angiogenesis of human microvascular endothelial cells through suppression of IL-8 production. Catechin 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12094614-0 2001 Green tea catechins and vitamin E inhibit angiogenesis of human microvascular endothelial cells through suppression of IL-8 production. Vitamin E 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 12094614-4 2001 In this model, the production of interleukin (IL)-8 by human microvascular endothelial cells at a low level of H2O2 was required for angiogenesis, as assessed by tube formation in three-dimensional gel in culture. Hydrogen Peroxide 111-115 C-X-C motif chemokine ligand 8 Homo sapiens 33-51 12094614-5 2001 Vitamin E (d-alpha-tocopherol, 40 microM) in the culture media significantly reduced IL-8 production and angiogenesis. Vitamin E 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 11565117-3 2001 The author considers, that interleukin-8 is connected with high concentration of oxygen active forms in neutrophils in the patients with this stage of disease. Oxygen 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 11137126-7 2000 Daily intramuscular treatment of GB piglets with 1mg/kg of FK506 from birth for 4 weeks resulted in lowered (P<0.05) in vitro secretion of interferon-gamma and interleukin-8. Tacrolimus 59-64 C-X-C motif chemokine ligand 8 Homo sapiens 163-176 11137126-9 2000 The depletions of mononuclear cells and low levels of interferon-gamma and interleukin-8 in piglets treated with FK506 were accompanied by lower proportion of CD3+, CD2+CD4+ and CD2+CD8+ T-cell phenotypes in peripheral blood but not in thymus and mesenteric lymph nodes. Tacrolimus 113-118 C-X-C motif chemokine ligand 8 Homo sapiens 75-88 11156586-0 2001 N-acetylcysteine attenuates TNF-alpha-induced p38 MAP kinase activation and p38 MAP kinase-mediated IL-8 production by human pulmonary vascular endothelial cells. Acetylcysteine 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 11156586-4 2001 However, the effect of N-acetylcysteine (NAC), which acts as a precursor of glutathione (GSH) synthesis, on TNF-alpha-induced activation of p38 MAP kinase pathway and p38 MAP kinase-mediated IL-8 production by human pulmonary vascular endothelial cells has not been determined. Acetylcysteine 23-39 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 11156586-4 2001 However, the effect of N-acetylcysteine (NAC), which acts as a precursor of glutathione (GSH) synthesis, on TNF-alpha-induced activation of p38 MAP kinase pathway and p38 MAP kinase-mediated IL-8 production by human pulmonary vascular endothelial cells has not been determined. Acetylcysteine 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 11156586-7 2001 Human pulmonary vascular endothelial cells that had been preincubated with NAC were stimulated with TNF-alpha and then the activation of p38 MAP kinase and MKK3/MKK6 in the cells and IL-8 concentrations in the culture supernatants were determined. Acetylcysteine 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 11156586-13 2001 NAC attenuated p38 MAP kinase-mediated IL-8 production by TNF-alpha-stimulated cells. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 11156586-15 2001 These results indicate that the cellular reduction and oxidation (redox) regulated by intracellular GSH is critical for TNF-alpha-induced activation of p38 MAP kinase pathway and p38 MAP kinase-mediated IL-8 production by human pulmonary vascular endothelial cells, and we emphasize that anti-oxidant therapy is an important strategy for the treatment of acute lung injury. Glutathione 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 11340307-0 2001 1,25-dihydroxyvitamin D3 differentially regulates IL-1alpha-stimulated IL-8 and MCP-1 mRNA expression and chemokine secretion by human primary proximal tubular epithelial cells. Calcitriol 0-24 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 11855786-13 2001 Increased production of IL-6 and IL-8 might have contributed to abnormalities in iron metabolism and it is probably due to overstimulation of macrophages. Iron 81-85 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 11746504-1 2001 The results reported here show that sodium fluoride (NaF) at low concentration (up to 10 microM) increased four times the proliferation rate of avian osteoblasts in culture. Sodium Fluoride 36-51 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 11746504-3 2001 However, NaF decreased the incorporation of 35S-sulfate into proteoglycans (PGs) synthesized by osteoblasts (60-65%). 35s-sulfate 44-55 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 11746504-4 2001 Also, we observed that PGs synthesized in the presence of NaF (50 microM) exhibited a higher sensitivity to chondroitinase ABC than PGs synthesized by osteoblasts in the absence of NaF, suggesting an increase in the chondroitin sulfate moieties associated with the core protein of PGs. Chondroitin Sulfates 216-235 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 12094614-5 2001 Vitamin E (d-alpha-tocopherol, 40 microM) in the culture media significantly reduced IL-8 production and angiogenesis. alpha-Tocopherol 11-29 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 12094614-6 2001 Among the green tea catechins, epigallocatechin (0.5-1 microM) was the most effective in reducing IL-8 production and inhibiting angiogenesis. Catechin 20-29 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 12094614-6 2001 Among the green tea catechins, epigallocatechin (0.5-1 microM) was the most effective in reducing IL-8 production and inhibiting angiogenesis. gallocatechol 31-47 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 12094614-7 2001 These results suggest that consumption of green tea catechins or supplemental intake of vitamin E may have preventive effects on tumor development, mediated, at least in part, through inhibition of angiogenesis via suppression of IL-8 production. Catechin 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 12094614-7 2001 These results suggest that consumption of green tea catechins or supplemental intake of vitamin E may have preventive effects on tumor development, mediated, at least in part, through inhibition of angiogenesis via suppression of IL-8 production. Vitamin E 88-97 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 11845301-5 2001 Interestingly, treatment of CF gland cells with the isoflavone genistein, a well known CFTR mutant Cl(-) channel stimulator, results in a significant decrease ( P < 0.001) in IL-8 production down to levels released by non-CF gland cells. Isoflavones 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 11845301-5 2001 Interestingly, treatment of CF gland cells with the isoflavone genistein, a well known CFTR mutant Cl(-) channel stimulator, results in a significant decrease ( P < 0.001) in IL-8 production down to levels released by non-CF gland cells. Genistein 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 11382084-2 2001 One such additive is sodium fluoride (NaF), which promotes bone formation, facilitating implant integration and success. Sodium Fluoride 21-36 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Sepharose 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Sepharose 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Sepharose 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Sepharose 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Cycloheximide 177-190 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Cycloheximide 177-190 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Cycloheximide 177-190 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Cycloheximide 177-190 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Dactinomycin 195-208 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Dactinomycin 195-208 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Dactinomycin 195-208 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-3 2000 Sepharose-immobilized IL-8 stimulated a sevenfold increase in IL-8 production within 2 h. IL-8 induced the expression of its own message, and IL-8 biosynthesis was inhibited by cycloheximide and actinomycin D, indicating de novo RNA and protein synthesis. Dactinomycin 195-208 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-6 2000 The involvement of mitogen-activated protein kinase (MAPK) in IL-8-induced IL-8 biosynthesis was suggested by the ability of PD-98059, an inhibitor of MAPK kinase, to block this function. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 11076803-6 2000 The involvement of mitogen-activated protein kinase (MAPK) in IL-8-induced IL-8 biosynthesis was suggested by the ability of PD-98059, an inhibitor of MAPK kinase, to block this function. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 11218494-10 2000 Our data indicate that the fluoride release from the resin-modified glass ionomer studied may be increased after treatment with an acidified NaF-toothpaste. Fluorides 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 11121511-12 2000 On the other hand, in certain local responses, and under certain conditions, catecholamines may actually boost regional immune responses, through induction of IL-1, tumor necrosis factor-alpha, and primarily IL-8 production. Catecholamines 77-91 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 11137464-4 2000 Two different fractions (ethanol or chloroform soluble extracts) of CSE with their chemical types identified showed a time- and dose-dependent increase on IL-8 secretion from ECV304 cell line. Ethanol 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 11137464-4 2000 Two different fractions (ethanol or chloroform soluble extracts) of CSE with their chemical types identified showed a time- and dose-dependent increase on IL-8 secretion from ECV304 cell line. Chloroform 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 11083814-5 2000 Furthermore, PMN stimulated by OMV in the presence of IFN-gamma demonstrated an enhanced capacity to release TNF-alpha, IL-1beta, IL-8, and MIP-1beta compared to stimulation with OMV alone. 1-ethylcyclopentyl [(2R,6S,12Z,13aS,14aR,16aS)-2-[(7-methoxy-3-methylquinoxalin-2-yl)oxy]-14a-{[(1-methylcyclopropyl)sulfonyl]carbamoyl}-5,16-dioxo-1,2,3,5,6,7,8,9,10,11,13a,14,14a,15,16,16a-hexadecahydrocyclopropa[e]pyrrolo[1,2-a][1,4]diazacyclopentadecin-6-yl]carbamate 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 11137464-6 2000 Protein tyrosine kinase (PTK) inhibitor genistein and protein kinase A (PKA) inhibitor H8 at respective concentrations significantly reduced chloroform and ethanol soluble extract-induced IL-8 expression by about 34 and 35% respectively at 8 h after incubation. N-(2-(methylamino)ethyl)-5-isoquinolinesulfonamide 87-89 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 11137464-6 2000 Protein tyrosine kinase (PTK) inhibitor genistein and protein kinase A (PKA) inhibitor H8 at respective concentrations significantly reduced chloroform and ethanol soluble extract-induced IL-8 expression by about 34 and 35% respectively at 8 h after incubation. Ethanol 156-163 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 11130495-13 2000 PAF priming of IL-8 responses was unaffected by injury. Platelet Activating Factor 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 11169058-0 2000 Neopterin and interleukin-8--prognosis in alcohol-induced cirrhosis. Alcohols 42-49 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 11169058-11 2000 CONCLUSIONS: Neopterin and IL-8 plasma levels are raised in patients with alcohol-induced cirrhosis, and are predictive of mortality associated with infections and upper gastrointestinal bleeding, respectively. Alcohols 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 11087880-12 2000 In the patients who received methylprednisolone, interleukin-8 concentrations decreased by 50 percent, and this decrease correlated with the duration of neuralgia and with the extent of global pain relief (P<0.001 for both comparisons). Methylprednisolone 29-47 C-X-C motif chemokine ligand 8 Homo sapiens 49-62 11192539-0 2000 N-acetyl-L-cysteine inhibits bleomycin-induced interleukin-8 secretion by bronchial epithelial cells. Bleomycin 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 11192539-6 2000 In the present study, we showed that BLM induced the expression of IL-8 protein and mRNA in BEAS-2B cells, and N-acetyl-L-cysteine (NAC) inhibited IL-8 expression. Bleomycin 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 11192539-6 2000 In the present study, we showed that BLM induced the expression of IL-8 protein and mRNA in BEAS-2B cells, and N-acetyl-L-cysteine (NAC) inhibited IL-8 expression. Bleomycin 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 11192539-7 2000 In addition, the structurally unrelated antioxidant, pyrrolidine dithiocarbamate (PDTC) also effectively inhibited BLM-induced IL-8 production. pyrrolidine dithiocarbamic acid 53-80 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 11192539-7 2000 In addition, the structurally unrelated antioxidant, pyrrolidine dithiocarbamate (PDTC) also effectively inhibited BLM-induced IL-8 production. pyrrolidine dithiocarbamic acid 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 11119262-0 2000 Enprostil, a prostaglandin-E(2) analogue, inhibits interleukin-8 production of human colonic epithelial cell lines. Enprostil 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 11119262-5 2000 Furthermore, 10(-6) M enprostil suppressed IL-8 production in HT-29 cells, SW620 and CaCo2 stimulated with interleukin-1 beta (IL-1 beta) or lipopolysaccharide (LPS), but did not suppress this response when cells were stimulated with tumour necrosis factor (TNF)-alpha. Enprostil 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 11084285-4 2000 Release of IL-8 was down-regulated by transforming growth factor beta2 (TGF-beta2), by the protein tyrosine-kinase inhibitor genistein, and via rises in intracellular cyclic AMP, generated by prostaglandin E(2), rolipram, pentoxifylline, forskolin, or dibutyryl-cyclic AMP. Pentoxifylline 222-236 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 11084285-4 2000 Release of IL-8 was down-regulated by transforming growth factor beta2 (TGF-beta2), by the protein tyrosine-kinase inhibitor genistein, and via rises in intracellular cyclic AMP, generated by prostaglandin E(2), rolipram, pentoxifylline, forskolin, or dibutyryl-cyclic AMP. Genistein 125-134 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 11084285-4 2000 Release of IL-8 was down-regulated by transforming growth factor beta2 (TGF-beta2), by the protein tyrosine-kinase inhibitor genistein, and via rises in intracellular cyclic AMP, generated by prostaglandin E(2), rolipram, pentoxifylline, forskolin, or dibutyryl-cyclic AMP. Colforsin 238-247 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 11084285-4 2000 Release of IL-8 was down-regulated by transforming growth factor beta2 (TGF-beta2), by the protein tyrosine-kinase inhibitor genistein, and via rises in intracellular cyclic AMP, generated by prostaglandin E(2), rolipram, pentoxifylline, forskolin, or dibutyryl-cyclic AMP. Cyclic AMP 167-177 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 11084285-4 2000 Release of IL-8 was down-regulated by transforming growth factor beta2 (TGF-beta2), by the protein tyrosine-kinase inhibitor genistein, and via rises in intracellular cyclic AMP, generated by prostaglandin E(2), rolipram, pentoxifylline, forskolin, or dibutyryl-cyclic AMP. Prostaglandins E 192-207 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 11084285-4 2000 Release of IL-8 was down-regulated by transforming growth factor beta2 (TGF-beta2), by the protein tyrosine-kinase inhibitor genistein, and via rises in intracellular cyclic AMP, generated by prostaglandin E(2), rolipram, pentoxifylline, forskolin, or dibutyryl-cyclic AMP. Bucladesine 252-272 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 11084285-4 2000 Release of IL-8 was down-regulated by transforming growth factor beta2 (TGF-beta2), by the protein tyrosine-kinase inhibitor genistein, and via rises in intracellular cyclic AMP, generated by prostaglandin E(2), rolipram, pentoxifylline, forskolin, or dibutyryl-cyclic AMP. Rolipram 212-220 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 11103787-5 2000 We show that thymidine induces oxidative stress in TP-overexpressing carcinoma cells, promoting secretion of the stress-induced angiogenic factors vascular endothelial growth factor and interleukin-8, and inducing matrix metalloproteinase-1. Thymidine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 186-199 11084285-5 2000 In addition, incubation with the synthetic glucocorticoid dexamethasone or suppression of activity of p38 mitogen-activated protein (MAP) kinases by SB-203580 modulated release of IL-8. Dexamethasone 58-71 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 11084285-5 2000 In addition, incubation with the synthetic glucocorticoid dexamethasone or suppression of activity of p38 mitogen-activated protein (MAP) kinases by SB-203580 modulated release of IL-8. SB 203580 149-158 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 11293246-6 2000 Thanks to clinical studies it has been performed that MTX holds up activity and productions of Il-8, releasing of TNF-alpha and reduction of concentration Il-6. Methotrexate 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 11048965-0 2000 Effect of phenytoin on the production of interleukin-6 and interleukin-8 in human gingival fibroblasts. Phenytoin 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 11046208-12 2000 Plasma IL-8 at 2 h correlated with NAG/creatinine at 6 h (P < 0.05). Creatinine 39-49 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 11069840-5 2000 IL-8 mRNA expression was significantly greater in tumor tissue; high expression was highly associated with tumor in advanced stages (p = 0.03), distant lymph node metastasis (p = 0.02), high tumor MC (> 123) (p = 0.00003), short survival (< 26 mo) (p < 0.00001), and early relapse (< 16 mo) (p < 0.00001). Methylcholanthrene 197-199 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 11050002-6 2000 Studies on the mechanism of KS tumor growth inhibition by 1alpha,25 dihydroxyvitamin D(3) showed that production of autocrine growth factors interleukin (IL)-6 and IL-8 was reduced in a dose-dependent manner, whereas no effect was observed on vascular endothelial growth factor and basic fibroblast growth factor. 1,25-dihydroxyvitamin D 58-86 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 12845334-3 2000 In addition, IL-8 release from eosinophils was inhibited by epinastine posttranscriptionally. epinastine 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 11053033-3 2000 Triptolide, with an IC(50) of approximately 20-50 ng/ml, inhibits normal and transformed human bronchial epithelial cell expression of interleukin (IL)-6 and IL-8 stimulated by phorbol 12-myristate 13-acetate (PMA), tumor necrosis factor-alpha, or IL-1 beta. triptolide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 11053033-3 2000 Triptolide, with an IC(50) of approximately 20-50 ng/ml, inhibits normal and transformed human bronchial epithelial cell expression of interleukin (IL)-6 and IL-8 stimulated by phorbol 12-myristate 13-acetate (PMA), tumor necrosis factor-alpha, or IL-1 beta. Tetradecanoylphorbol Acetate 177-208 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 11053033-4 2000 Nuclear runoff and luciferase reporter gene assays demonstrate that triptolide inhibits IL-8 transcription. triptolide 68-78 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 11053033-6 2000 A cDNA array and clustering algorithm analysis reveals that triptolide inhibits expression of the PMA-induced genes tumor necrosis factor-alpha, IL-8, macrophage inflammatory protein-2 alpha, intercellular adhesion molecule-1, integrin beta(6), vascular endothelial growth factor, granulocyte-macrophage colony-stimulating factor, GATA-3, fra-1, and NF45. triptolide 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 11052920-6 2000 Ciprofloxacin decreased IL-6 mRNA (P<0.05) and increased IL-8 mRNA (P<0.05) expression. Ciprofloxacin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 11052920-10 2000 Increased IL-8 mRNA in response to ciprofloxacin was not reflected by altered transcription factor activation and may represent increased mRNA stability. Ciprofloxacin 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 11246821-6 2000 Ciglitazone 10-100 M inhibited interleukin-8 release by 25-33% (p < 0.05) and mRNA expression by 33-60% (p < 0.05). ciglitazone 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 31-44 11246821-7 2000 Metformin 0.1-10 mM inhibited interleukin-8 release by 20-50% (p < 0.05) and mRNA expression by 20-90% (p < 0.05). Metformin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 11046054-4 2000 Rhinovirus infection induced a time- and dose-dependent increase in tyrosine phosphorylation of p38 kinase, which peaked 30 min postinfection and remained elevated for 1 h. Treatment of infected cells with SB 239063, a potent pyridinyl imidazole inhibitor of p38 kinase, resulted in up to 100% inhibition of mediator production and partially reduced levels of IL-8 mRNA as determined by quantitative RT-PCR. SB 239063 206-215 C-X-C motif chemokine ligand 8 Homo sapiens 360-364 11053499-0 2000 Medium- and long-chain fatty acids differentially modulate interleukin-8 secretion in human fetal intestinal epithelial cells. medium- and long-chain fatty acids 0-34 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 11053499-3 2000 In the present study, we evaluated the effects of medium-chain and long-chain fatty acids (MCFA and LCFA) on interleukin (IL)-8 secretion in a fetal intestinal epithelial cell line, intestine-407 cells. and long-chain fatty acids 63-89 C-X-C motif chemokine ligand 8 Homo sapiens 109-127 11053499-3 2000 In the present study, we evaluated the effects of medium-chain and long-chain fatty acids (MCFA and LCFA) on interleukin (IL)-8 secretion in a fetal intestinal epithelial cell line, intestine-407 cells. mcfa 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 109-127 11053499-6 2000 The addition of oleic acid (LCFA) micelles, but not octanoic acid (MCFA) micelles, weakly but significantly enhanced basal IL-8 secretion in the intestine-407 cells. Oleic Acid 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 11048965-1 2000 The in vitro effect of phenytoin (PHT) on the production of interleukin-6 (IL-6) and interleukin-8 (IL-8) in human gingival fibroblasts, challenged with or without interleukin-1beta (IL-1beta), was studied. Phenytoin 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 85-98 11053499-6 2000 The addition of oleic acid (LCFA) micelles, but not octanoic acid (MCFA) micelles, weakly but significantly enhanced basal IL-8 secretion in the intestine-407 cells. lcfa 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 11048965-1 2000 The in vitro effect of phenytoin (PHT) on the production of interleukin-6 (IL-6) and interleukin-8 (IL-8) in human gingival fibroblasts, challenged with or without interleukin-1beta (IL-1beta), was studied. Phenytoin 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 11053499-7 2000 The addition of MCFA (5 mmol/L) induced a 40% increase in IL-1beta-induced IL-8 secretion and a 35% increase in tumor necrosis factor (TNF)-alpha-induced IL-8 secretion, respectively. mcfa 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 11053499-7 2000 The addition of MCFA (5 mmol/L) induced a 40% increase in IL-1beta-induced IL-8 secretion and a 35% increase in tumor necrosis factor (TNF)-alpha-induced IL-8 secretion, respectively. mcfa 16-20 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 11048965-4 2000 The anti-inflammatory drug, dexamethasone (1 microM), abolished the production of both IL-6 and IL-8 in gingival fibroblasts challenged with PHT in the presence or absence of IL-1beta. Dexamethasone 28-41 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 11048965-4 2000 The anti-inflammatory drug, dexamethasone (1 microM), abolished the production of both IL-6 and IL-8 in gingival fibroblasts challenged with PHT in the presence or absence of IL-1beta. Phenytoin 141-144 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 11030960-0 2000 Observation of anti-stokes fluorescence cooling in thulium-doped glass We report the first observation of anti-Stokes fluorescence cooling in a thulium-doped solid with pump excitation at 1.82 &mgr;m<lambda<1.97 &mgr;m. At a pump wavelength of 1.9 &mgr;m and incident average power of approximately 3 W, a Tm3+:ZBLANP ( ZrF4-BaF2-LaF3-AlF3-NaF-PbF2) sample cooled to -1.2 degrees C from room temperature for a single pass of the pump beam. Thulium 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 358-361 11069732-13 2000 As previously reported, the inhibition of NO synthesis by the competitive inhibitor L-NMMA led to enhancement of IL-6, IL-8 and PGE(2)production by IL-1 beta treated chondrocytes, but did not significantly modify IL-10, PG and MMP-3 productions. omega-N-Methylarginine 84-90 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 11105996-7 2000 Inclusion of 5/1000 (86 mM) ethanol in the medium reduced tumour necrosis factor (TNF)-alpha and interleukin (IL)-8 production in human mast cell line (HMC-1) cells by 55 +/- 7% and 19 +/- 5%, respectively, and the presence of 20/1000 (344 mM) ethanol inhibited the expression 81 +/- 12% and 59 +/- 14% respectively. Ethanol 28-35 C-X-C motif chemokine ligand 8 Homo sapiens 97-115 11030960-0 2000 Observation of anti-stokes fluorescence cooling in thulium-doped glass We report the first observation of anti-Stokes fluorescence cooling in a thulium-doped solid with pump excitation at 1.82 &mgr;m<lambda<1.97 &mgr;m. At a pump wavelength of 1.9 &mgr;m and incident average power of approximately 3 W, a Tm3+:ZBLANP ( ZrF4-BaF2-LaF3-AlF3-NaF-PbF2) sample cooled to -1.2 degrees C from room temperature for a single pass of the pump beam. Thulium 144-151 C-X-C motif chemokine ligand 8 Homo sapiens 358-361 11037876-0 2000 The mechanism of taurine chloramine inhibition of cytokine (interleukin-6, interleukin-8) production by rheumatoid arthritis fibroblast-like synoviocytes. chloramine 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 75-88 11031216-10 2000 Incubation of ECs with N:-acetyl cysteine inhibited production of IL-8 and MCP-1 induced by LDL(-) and oxLDL by >50%. Acetylcysteine 23-41 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 11196946-0 2000 Matrix-isolated Al2OF6(2-) ion in molten and solid LiF/NaF/KF. al2of6(2-) 16-26 C-X-C motif chemokine ligand 8 Homo sapiens 55-58 11196946-1 2000 A Raman spectrum consistent with that expected from an Al2OF6(2-) ion was observed when Na2O was dissolved in a eutectic LiF/NaF/KF (FLINAK) melt at 500 degrees C, which contained a low concentration of either AlF3 or Na3AlF6. sodium oxide 88-92 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 11031216-9 2000 Actinomycin D inhibited the release of IL-8 and MCP-1 induced by LDL(-) and oxLDL by up to 80%, indicating that their production is mediated by protein synthesis. Dactinomycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 11037876-1 2000 OBJECTIVE: Taurine chloramine (Tau-Cl) has been shown to inhibit the production of proinflammatory cytokines (interleukin-6 [IL-6] and IL-8) by fibroblast-like synoviocytes (FLS) isolated from rheumatoid arthritis (RA) patients. Taurine 11-18 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 11037876-1 2000 OBJECTIVE: Taurine chloramine (Tau-Cl) has been shown to inhibit the production of proinflammatory cytokines (interleukin-6 [IL-6] and IL-8) by fibroblast-like synoviocytes (FLS) isolated from rheumatoid arthritis (RA) patients. chloramine 19-29 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 11037876-1 2000 OBJECTIVE: Taurine chloramine (Tau-Cl) has been shown to inhibit the production of proinflammatory cytokines (interleukin-6 [IL-6] and IL-8) by fibroblast-like synoviocytes (FLS) isolated from rheumatoid arthritis (RA) patients. N-chlorotaurine 31-37 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 11032978-2 2000 METHODS: To test this hypothesis, the beta-adrenergic agonist, isoproterenol, and the G protein activator, sodium fluoride (NaF), were used to stimulate cAMP production in B lymphoblasts from healthy and BP-I subjects phenotyped on basal intracellular calcium concentration ([Ca(2+)](B)). Sodium Fluoride 107-122 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 11032978-2 2000 METHODS: To test this hypothesis, the beta-adrenergic agonist, isoproterenol, and the G protein activator, sodium fluoride (NaF), were used to stimulate cAMP production in B lymphoblasts from healthy and BP-I subjects phenotyped on basal intracellular calcium concentration ([Ca(2+)](B)). Cyclic AMP 153-157 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 11037876-3 2000 METHODS: The effects of Tau-Cl on 1) the transcription of genes coding for IL-6 and IL-8, and 2) the activity of nuclear factor kappaB (NF-kappaB) and activator protein 1 (AP-1) transcription factors, which are crucial for the transcription of these cytokine genes, were investigated in FLS isolated from the synovial tissue of RA patients. N-chlorotaurine 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 11032978-5 2000 Although basal and NaF-stimulated cAMP production was greater in B lymphoblast membranes from male BP-I patients with high versus normal [Ca(2+)](B), there were no differences in the percent stimulation. Cyclic AMP 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 11037876-8 2000 Tau-Cl, but not Tau, reduced IL-1beta-triggered cytokine mRNA expression, exerting stronger inhibitory activity on the levels of IL-6 than on those of IL-8. N-chlorotaurine 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 11037876-0 2000 The mechanism of taurine chloramine inhibition of cytokine (interleukin-6, interleukin-8) production by rheumatoid arthritis fibroblast-like synoviocytes. Taurine 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 75-88 11079780-8 2000 R-838 also inhibited interleukin-8 release from HBECs. r-838 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 11012615-8 2000 The induction of IL-8 mRNA by poly-L-arginine was significantly inhibited by actinomycin D. polyarginine 30-45 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11012615-8 2000 The induction of IL-8 mRNA by poly-L-arginine was significantly inhibited by actinomycin D. Dactinomycin 77-90 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 11023990-13 2000 IL-8 and SDF-1alpha but not IP-10 induced calcium mobilization in adherent ECs, suggesting that signaling events associated with calcium mobilization are separable from those required for chemotaxis. Calcium 129-136 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10979935-4 2000 The present study demonstrates that amphotericin B increases mRNA for the chemokines interleukin (IL)-8, monocyte chemoattractant protein (MCP)-1, and macrophage inflammatory protein (MIP)-1beta, as well as the cell adhesion molecules intercellular adhesion molecule (ICAM)-1 and CD44 in the human monocytic cell line THP-1. Amphotericin B 36-50 C-X-C motif chemokine ligand 8 Homo sapiens 85-103 10979935-5 2000 Amphotericin B increased the concentrations of IL-8, MCP-1, and MIP-1beta in a dose-dependent fashion. Amphotericin B 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 11037761-6 2000 None or weakly toxic concentrations of Ni and Co chloride induced IL-6 and IL-8 release by a factor of 5-10 compared to controls. co chloride 46-57 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 10979965-8 2000 Secretion of IL-8 reached a plateau level in less than 24 hours, was inhibited by cycloheximide, and required the presence of HrHRF throughout the culture period. Cycloheximide 82-95 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 11027515-0 2000 Reactive oxygen intermediates are involved in IL-8 production induced by hyperosmotic stress in human bronchial epithelial cells. reactive oxygen 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 11027515-3 2000 Hyperosmolarity (NaCl) caused a time- and concentration-dependent increase in IL-8 expression and secretion in bronchial epithelial cells. Sodium Chloride 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 11027515-4 2000 These effects could be blocked by antioxidants, such as DMSO, DMTU, DTT, and beta-mercaptoethanol, suggesting an involvement of reactive oxygen intermediates (ROI) in the signal transduction of hyperosmolarity-induced IL-8 synthesis. Mercaptoethanol 77-97 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 10982368-9 2000 Tat(72aa)-mediated MCP-1 and IL-8 mRNA induction was susceptible to inhibition by the MEK1/2 inhibitor UO126 but was only modestly decreased by the inclusion of the p38 mitogen-activated protein kinase (MAPK) inhibitor SB202190. U 0126 103-108 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10982368-9 2000 Tat(72aa)-mediated MCP-1 and IL-8 mRNA induction was susceptible to inhibition by the MEK1/2 inhibitor UO126 but was only modestly decreased by the inclusion of the p38 mitogen-activated protein kinase (MAPK) inhibitor SB202190. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 219-227 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 11015126-0 2000 Effects of early inhaled beclomethasone therapy on tracheal aspirate inflammatory mediators IL-8 and IL-1ra in ventilated preterm infants at risk for bronchopulmonary dysplasia. Beclomethasone 25-39 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 11015126-7 2000 Median IL-8 levels were lower in beclomethasone versus placebo infants on study days 8 (82.9 vs. 209.2, P < 0.01) and 15 (37.4 vs. 77.4, P < 0.03) after controlling for antenatal glucocorticoid therapy and maternal race. Beclomethasone 33-47 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 11015126-9 2000 Fewer beclomethasone infants with baseline IL-8 levels in the interquartile range required systemic glucocorticoid therapy (beclomethasone 30.6% vs. placebo 65.8%, P < 0.01) or developed BPD (beclomethasone 42.4% vs. placebo 69.4%, P < 0.03). Beclomethasone 6-20 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 11015126-11 2000 Beclomethasone-treated infants with moderately elevated baseline IL-8 levels received less subsequent systemic glucocorticoid therapy and had a lower incidence of BPD than nontreated infants. Beclomethasone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 11175566-1 2000 OBJECTIVE: The aims of this article are to verify if there is any alteration in the secretion of natriuretic atrial factor (NAF) in children submitted to mechanical pulmonary ventilation and if these possible alterations would lead to modification in the urinary volume and in the urinary sodium excretion. Sodium 289-295 C-X-C motif chemokine ligand 8 Homo sapiens 97-122 11175566-1 2000 OBJECTIVE: The aims of this article are to verify if there is any alteration in the secretion of natriuretic atrial factor (NAF) in children submitted to mechanical pulmonary ventilation and if these possible alterations would lead to modification in the urinary volume and in the urinary sodium excretion. Sodium 289-295 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 10988245-0 2000 Role for peroxisome proliferator-activated receptor alpha in oxidized phospholipid-induced synthesis of monocyte chemotactic protein-1 and interleukin-8 by endothelial cells. Phospholipids 70-82 C-X-C motif chemokine ligand 8 Homo sapiens 139-152 10988245-3 2000 In the present study, we demonstrate that MM-LDL and oxidation products of 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphocholine (PAPC) activate endothelial cells to synthesize monocyte chemotactic protein-1 (MCP-1) and interleukin-8 (IL-8). PC(16:0/20:0) 75-128 C-X-C motif chemokine ligand 8 Homo sapiens 220-233 10988245-3 2000 In the present study, we demonstrate that MM-LDL and oxidation products of 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphocholine (PAPC) activate endothelial cells to synthesize monocyte chemotactic protein-1 (MCP-1) and interleukin-8 (IL-8). PC(16:0/20:0) 75-128 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 10988245-3 2000 In the present study, we demonstrate that MM-LDL and oxidation products of 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphocholine (PAPC) activate endothelial cells to synthesize monocyte chemotactic protein-1 (MCP-1) and interleukin-8 (IL-8). PAPC 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 220-233 10975802-8 2000 Octreotide, which mainly stimulates somatostatin receptor subtypes 2 and 5, affected the secretion of IL-8 and IL-1beta similarly, and the somatostatin antagonist cyclo-somatostatin completely blocked the somatostatin- and octreotide-induced inhibitory effects. Octreotide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 10988245-3 2000 In the present study, we demonstrate that MM-LDL and oxidation products of 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphocholine (PAPC) activate endothelial cells to synthesize monocyte chemotactic protein-1 (MCP-1) and interleukin-8 (IL-8). PAPC 130-134 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 10988245-7 2000 By contrast, troglitazone, a PPARgamma agonist, decreased the levels of IL-8 and MCP-1. Troglitazone 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 10984371-9 2000 RESULTS: Calcium influx was induced by monocyte chemotactic protein (MCP) 1, MCP-3, MCP-4, RANTES, eotaxin, IL-8, and stromal cell-derived factor 1alpha, which are chemokines that bind several chemokine receptors. Calcium 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 11014907-1 2000 Sodium monofluorophosphate (NaMFP) and sodium fluoride (NaF) are the two most common sources of fluoride used in currently marketed fluoride dentifrices. Sodium Fluoride 39-54 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 11014907-1 2000 Sodium monofluorophosphate (NaMFP) and sodium fluoride (NaF) are the two most common sources of fluoride used in currently marketed fluoride dentifrices. Fluorides 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 11014907-1 2000 Sodium monofluorophosphate (NaMFP) and sodium fluoride (NaF) are the two most common sources of fluoride used in currently marketed fluoride dentifrices. Fluorides 96-104 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 11014907-2 2000 The purpose of this study was to investigate the effect of mouth rinses containing NaF or NaMFP on the concentrations of fluoride, or the MFP ion, in saliva, whole plaque, and plaque fluid. Fluorides 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 11014907-10 2000 Although there was a very large range in these measurements, fluoride in plaque fluid (excluding fluoride in unhydrolyzed MFP) and whole plaque were significantly (p<0.05) greater after the NaF rinse at all time periods. Fluorides 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 193-196 11014907-11 2000 In saliva, the NaF rinse produced a statistically significant greater salivary fluoride (excluding fluoride in unhydrolyzed MFP) only at 60 min. Fluorides 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 11014907-11 2000 In saliva, the NaF rinse produced a statistically significant greater salivary fluoride (excluding fluoride in unhydrolyzed MFP) only at 60 min. Fluorides 99-107 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 10976010-6 2000 Serum IL-8 values increased after alcohol intake in healthy subjects. Alcohols 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 11022126-3 2000 Control experiments revealed that 10- 6 M dexamethasone inhibited the TNF-alpha- or IL-1beta-mediated increase of IL-8 mRNA in A549 cells, which showed that the glucocorticoid was functional. Dexamethasone 42-55 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 10996027-5 2000 Co-injection of BA with CXC chemokine interleukin-8 (IL-8) into rat skin significantly inhibited IL-8 elicited neutrophil infiltration. baicalin 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 10996027-5 2000 Co-injection of BA with CXC chemokine interleukin-8 (IL-8) into rat skin significantly inhibited IL-8 elicited neutrophil infiltration. baicalin 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10996027-7 2000 This conclusion was supported by the fact that BA cross-linked to oxime resin bound chemokines of the CXC (stromal cell-derived factor (SDF)-1alpha, IL-8), CC (macrophage inflammatory protein (MIP)-1beta, monocyte chemotactic protein (MCP)-2), and C (lymphotactin (Ltn)) subfamilies. baicalin 47-49 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 10996027-7 2000 This conclusion was supported by the fact that BA cross-linked to oxime resin bound chemokines of the CXC (stromal cell-derived factor (SDF)-1alpha, IL-8), CC (macrophage inflammatory protein (MIP)-1beta, monocyte chemotactic protein (MCP)-2), and C (lymphotactin (Ltn)) subfamilies. Oximes 66-71 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 10975857-2 2000 We evaluated the role of NF-kappaB in HRV-16-induced IL-8 and IL-6 production by EMSA using oligonucleotides corresponding to the binding sites for NF-kappaB in the IL-6 and IL-8 gene promoters. Oligonucleotides 92-108 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 10975857-3 2000 Consistent with the rapid induction of mRNA for IL-8 and IL-6, maximal NF-kappaB binding to both oligonucleotides was detected at 30 min after infection. Oligonucleotides 97-113 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 10975857-5 2000 The IL-8 oligonucleotide bound recombinant p50 with only about one-tenth the efficiency of the IL-6 oligonucleotide, even though epithelial cells produced more IL-8 protein than IL-6. Oligonucleotides 9-24 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 10975857-5 2000 The IL-8 oligonucleotide bound recombinant p50 with only about one-tenth the efficiency of the IL-6 oligonucleotide, even though epithelial cells produced more IL-8 protein than IL-6. Oligonucleotides 9-24 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 10975857-5 2000 The IL-8 oligonucleotide bound recombinant p50 with only about one-tenth the efficiency of the IL-6 oligonucleotide, even though epithelial cells produced more IL-8 protein than IL-6. Oligonucleotides 100-115 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 10973631-6 2000 FK506 and cyclosporin A suppressed the chemotactic activity of the supernatant in parallel to the suppression of interleukin-8 production by peripheral blood mononuclear cells. Tacrolimus 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 10973631-6 2000 FK506 and cyclosporin A suppressed the chemotactic activity of the supernatant in parallel to the suppression of interleukin-8 production by peripheral blood mononuclear cells. Cyclosporine 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 10973631-8 2000 These studies indicate that FK506 may exert a beneficial effect on human inflammatory diseases by suppressing neutrophil chemotaxis secondary to inhibition of chemoattractant (for example, interleukin-8) production by leukocytes. Tacrolimus 28-33 C-X-C motif chemokine ligand 8 Homo sapiens 189-202 11028659-8 2000 Furthermore, PD98059 or SB203580 significantly suppressed BK-induced IL-6 and IL-8 production and their gene expression. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 11028659-8 2000 Furthermore, PD98059 or SB203580 significantly suppressed BK-induced IL-6 and IL-8 production and their gene expression. SB 203580 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 10950803-4 2000 Thalidomide treatment was found to cause potent and selective inhibition of IL-8 production in a dose-responsive manner. Thalidomide 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 10950803-6 2000 In addition, thalidomide treatment of lipopolysaccharide-stimulated microglia inhibited the activation of protein NF-kappaB, a transcription factor known to be important for IL-8 production. Thalidomide 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 10950803-7 2000 These results suggest thalidomide could have a therapeutic role in acute bacterial meningitis through inhibition of IL-8-mediated neutrophil chemotaxis. Thalidomide 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 10958731-12 2000 In vitro studies demonstrated that SK-N-MC and SK-N-SH cells express low levels of IL-8 under normal conditions and that IL-1beta and tumor necrosis factor-alpha significantly increased expression of IL-8 at 24 and 48 hours. sk-n-mc 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 10958731-12 2000 In vitro studies demonstrated that SK-N-MC and SK-N-SH cells express low levels of IL-8 under normal conditions and that IL-1beta and tumor necrosis factor-alpha significantly increased expression of IL-8 at 24 and 48 hours. sk-n 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 10958731-12 2000 In vitro studies demonstrated that SK-N-MC and SK-N-SH cells express low levels of IL-8 under normal conditions and that IL-1beta and tumor necrosis factor-alpha significantly increased expression of IL-8 at 24 and 48 hours. sk-n 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 11108140-3 2000 Activation of heterotrimeric G proteins with NaF resulted in a divergent signaling effect; NaF treatment was sufficient to increase tyrosine phosphorylation levels of some proteins independent of angiotensin II treatment. Tyrosine 132-140 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 11108140-4 2000 In the same cells, NaF alone had no effect on other cellular proteins, but greatly potentiated the ability of angiotensin II to increase the tyrosine phosphorylation levels of these proteins. Tyrosine 141-149 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 11108140-6 2000 We found that NaF treatment alone, independent of angiotensin II stimulation, was sufficient to increase the tyrosine phosphorylation levels of paxillin. Tyrosine 109-117 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 11108140-7 2000 Furthermore, the ability of either NaF and/or angiotensin II to increase tyrosine phosphorylation levels of paxillin is critically dependent on intracellular Ca2+. Tyrosine 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 10964761-6 2000 Cotreatment with PDTC and curcumin reduced particle-elicited IL-8 response, whereas cycloheximide caused enhancement of IL-8 mRNA expression in both the quartz- and TiO(2)-treated cells. Curcumin 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 10989889-1 2000 Antimony oxide trihalides, SbOX3 molecules, where X = F or Cl have been produced, by means of an on-line process, using antimony trichloride, SbOCl3 as starting material passed over heated silver oxide at 230 degrees C. The antimony oxide trichloride SbOCl3 formed is then reacted with sodium fluoride, NaF at 550 degrees C to produce antimony oxide trifluoride, SbOF3. antimony oxide trihalides 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 303-306 11028544-11 2000 Incubation of TNFalpha + p38-mitogen-activated protein kinase (MAPK) inhibitor SB202190 increased apoptosis (P < 0.01) and decreased IL-8 production to PMN control. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 11028544-12 2000 To a lesser extent, incubation of TNFalpha with inhibitors to NF-kappaB (SN50) and PI3K (LY294002) also increased apoptosis and decreased IL-8 production (P < 0.05). 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 11028546-0 2000 Dopamine attenuates the chemoattractant effect of interleukin-8: a novel role in the systemic inflammatory response syndrome. Dopamine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 10964761-6 2000 Cotreatment with PDTC and curcumin reduced particle-elicited IL-8 response, whereas cycloheximide caused enhancement of IL-8 mRNA expression in both the quartz- and TiO(2)-treated cells. Cycloheximide 84-97 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 10930303-5 2000 Stimulation with lipopolysaccharide (LPS) or tetradecanoyl phorbol acetate (TPA) significantly increased the IL-8 level secreted by all cell lines; the best producers were TPA-treated MONO-MAC-6 and MUTZ-3 cultures, generating more than 50 000 pg/ml IL-8. Tetradecanoylphorbol Acetate 45-74 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10956206-3 2000 Additionally, the BTPs show inhibition of IL-4, IL-5, IL-8, and eotaxin production. btps 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 10900160-10 2000 We conclude that Na(2)SO(3) can activate human neutrophils and that its proinflammatory potential is further supported by its ability to increase IL-8 production. sodium sulfite 17-27 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 10930303-5 2000 Stimulation with lipopolysaccharide (LPS) or tetradecanoyl phorbol acetate (TPA) significantly increased the IL-8 level secreted by all cell lines; the best producers were TPA-treated MONO-MAC-6 and MUTZ-3 cultures, generating more than 50 000 pg/ml IL-8. Tetradecanoylphorbol Acetate 45-74 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 10930303-5 2000 Stimulation with lipopolysaccharide (LPS) or tetradecanoyl phorbol acetate (TPA) significantly increased the IL-8 level secreted by all cell lines; the best producers were TPA-treated MONO-MAC-6 and MUTZ-3 cultures, generating more than 50 000 pg/ml IL-8. Tetradecanoylphorbol Acetate 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10930303-5 2000 Stimulation with lipopolysaccharide (LPS) or tetradecanoyl phorbol acetate (TPA) significantly increased the IL-8 level secreted by all cell lines; the best producers were TPA-treated MONO-MAC-6 and MUTZ-3 cultures, generating more than 50 000 pg/ml IL-8. Tetradecanoylphorbol Acetate 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 10930303-5 2000 Stimulation with lipopolysaccharide (LPS) or tetradecanoyl phorbol acetate (TPA) significantly increased the IL-8 level secreted by all cell lines; the best producers were TPA-treated MONO-MAC-6 and MUTZ-3 cultures, generating more than 50 000 pg/ml IL-8. Tetradecanoylphorbol Acetate 172-175 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10930303-5 2000 Stimulation with lipopolysaccharide (LPS) or tetradecanoyl phorbol acetate (TPA) significantly increased the IL-8 level secreted by all cell lines; the best producers were TPA-treated MONO-MAC-6 and MUTZ-3 cultures, generating more than 50 000 pg/ml IL-8. Tetradecanoylphorbol Acetate 172-175 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 10930303-7 2000 The glucocorticoid dexamethasone and the protein kinase inhibitor staurosporine distinctively inhibited the IL-8 production of MONO-MAC-6 cells. Dexamethasone 19-32 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 10930303-7 2000 The glucocorticoid dexamethasone and the protein kinase inhibitor staurosporine distinctively inhibited the IL-8 production of MONO-MAC-6 cells. Staurosporine 66-79 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 10930308-0 2000 Nuclear factor-kappa b activation in silica-induced interleukin 8 production by human bronchial epithelial cells. Silicon Dioxide 37-43 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 10930308-1 2000 Recent studies indicate that interleukin 8 (IL-8) plays an important role in interstitial lung diseases including silica-induced lung inflammation. Silicon Dioxide 114-120 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 10930308-1 2000 Recent studies indicate that interleukin 8 (IL-8) plays an important role in interstitial lung diseases including silica-induced lung inflammation. Silicon Dioxide 114-120 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 10930308-4 2000 The administration of silica induced IL-8 production in BET-1A dose-dependently and time-dependently. Silicon Dioxide 22-28 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 10930308-5 2000 Northern blot analysis demonstrated that silica upregulated IL-8 expression in BET-1A. Silicon Dioxide 41-47 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 10951245-5 2000 Treatment of PAF-receptor-expressing KB cells with the metabolically stable PAF receptor agonist carbamoyl-PAF resulted in increased interleukin-8 mRNA and protein, indicating that activation of the epidermal PAF receptor was linked to interleukin-8 production. carbamoyl-paf 97-110 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 10983632-0 2000 Somatostatin (SOM) and octreotide (OCT) inhibit the secretion of interleukin-8 (IL-8) from human peripheral blood mononuclear cells (PBMC) in vitro. Octreotide 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 10983632-0 2000 Somatostatin (SOM) and octreotide (OCT) inhibit the secretion of interleukin-8 (IL-8) from human peripheral blood mononuclear cells (PBMC) in vitro. Octreotide 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 10928984-3 2000 The pan-COX inhibitor ketorolac continuously and significantly decreased PGE(2) production and IL-6 and IL-8 levels in all OPC cell lines tested, but did not affect IL-1alpha, GM-CSF levels, or in vitro tumor cell growth. Ketorolac 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 10983632-0 2000 Somatostatin (SOM) and octreotide (OCT) inhibit the secretion of interleukin-8 (IL-8) from human peripheral blood mononuclear cells (PBMC) in vitro. Octreotide 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 10983632-0 2000 Somatostatin (SOM) and octreotide (OCT) inhibit the secretion of interleukin-8 (IL-8) from human peripheral blood mononuclear cells (PBMC) in vitro. Octreotide 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 11008723-14 2000 After stimulation of HPMC, interleukin-8 secretion to the apical compartment increased in a time-dependent fashion, resulting in a gradient between the two chambers. hydroxypropylmethylcellulose-lactose matrix 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 10951245-5 2000 Treatment of PAF-receptor-expressing KB cells with the metabolically stable PAF receptor agonist carbamoyl-PAF resulted in increased interleukin-8 mRNA and protein, indicating that activation of the epidermal PAF receptor was linked to interleukin-8 production. carbamoyl-paf 97-110 C-X-C motif chemokine ligand 8 Homo sapiens 236-249 10951245-8 2000 Similarly, treatment of the PAF-receptor-expressing primary cultures of human keratinocytes or the human epidermal cell line A-431 with carbamoyl-PAF or ultraviolet B radiation resulted in interleukin-8 production that was partially inhibited by PAF receptor antagonists. carbamoyl-paf 136-149 C-X-C motif chemokine ligand 8 Homo sapiens 189-202 10951249-5 2000 Variable release of tumor necrosis factor-alpha and interleukin-8 from keratinocytes occurred only at toxic threshold concentrations of the phenols or sodium dodecyl sulfate. Phenols 140-147 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 10951249-5 2000 Variable release of tumor necrosis factor-alpha and interleukin-8 from keratinocytes occurred only at toxic threshold concentrations of the phenols or sodium dodecyl sulfate. Sodium Dodecyl Sulfate 151-173 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 11030461-1 2000 Naftidrofuryl (Praxilene; NAF) significantly improves claudication distance in patients with peripheral vascular disease (PVD). Nafronyl 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 10917982-17 2000 Regarding cytokine release, although a tendency toward high tumor necrosis factor alpha and interleukin-8 levels was noticed in the EAAA group, global time course effects failed to reach statistical significance (P =.543 and P =.080). eaaa 132-136 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 11030461-5 2000 NAF also inhibited (P <0.0001) shape change (PSC; an early phase of platelet activation, characterised by an increase in MPV) induced by ET-1 (0.4 micromol/l) in combination with ADP (0.05-0.15 micromol/l) or serotonin (0.03-0.13 micromol/ l). Adenosine Diphosphate 182-185 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 11030461-5 2000 NAF also inhibited (P <0.0001) shape change (PSC; an early phase of platelet activation, characterised by an increase in MPV) induced by ET-1 (0.4 micromol/l) in combination with ADP (0.05-0.15 micromol/l) or serotonin (0.03-0.13 micromol/ l). Serotonin 212-221 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 11778258-5 2000 Compared with the HNS group, there was a significant increase in the PMN and the level of IL-8 in the HS group (P < 0.05). hassio 102-104 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 11778258-8 2000 In the HS group the sputum level of IL-8 was also correlated positively with the PMN (rs = 0.8424). hassio 7-9 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 10893219-4 2000 Maximal IL-8 release was achieved with 10 ng/ml of TGF-beta1 after 16 h of incubation, which was inhibited by the transcription inhibitor actinomycin D and the corticosteroid dexamethasone but was not affected by the nonselective COX inhibitor indomethacin and the selective COX-2 inhibitor NS-398 despite their inhibition on TGF-beta1-induced PGE(2) release. Dactinomycin 138-151 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 10887141-5 2000 Fibroblasts grown from synovial and peritoneal tissues displayed C5a/IL-8-inhibitor activity that could be further induced with phorbol myristate acetate (PMA) and IL-1 beta. Tetradecanoylphorbol Acetate 128-153 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 10887141-5 2000 Fibroblasts grown from synovial and peritoneal tissues displayed C5a/IL-8-inhibitor activity that could be further induced with phorbol myristate acetate (PMA) and IL-1 beta. Tetradecanoylphorbol Acetate 155-158 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 10873156-0 2000 Synergistic inhibition by beta(2)-agonists and corticosteroids on tumor necrosis factor-alpha-induced interleukin-8 release from cultured human airway smooth-muscle cells. beta(2) 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 10873156-2 2000 Here, we tested the effects of the beta(2)-agonists salbutamol (Salbu) and salmeterol (Salme) on IL-8 release and tumor necrosis factor (TNF)-alpha-induced IL-8 release from ASM cells. beta(2) 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10933164-9 2000 In contrast, IL-8 mRNA expression of bronchial cells was significantly higher in the BOS group (0.85+/-0.40 vs. 0.22+/-0.10 O.D./O.D. N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 10873668-7 2000 The lack of the chemokine binding was not likely to be due to the lack of glycosylation of the Fy/GPA, since IL-8 was effectively bound to de-N-glycosylated erythrocytes. Nitrogen 142-143 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10873157-5 2000 Expression of IL-6 and IL-8 was sensitive to SB203580, the specific inhibitor of p38 mitogen-activated protein (MAP) kinase and PD98059, an inhibitor of MAP kinase kinase. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 128-135 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 10893219-4 2000 Maximal IL-8 release was achieved with 10 ng/ml of TGF-beta1 after 16 h of incubation, which was inhibited by the transcription inhibitor actinomycin D and the corticosteroid dexamethasone but was not affected by the nonselective COX inhibitor indomethacin and the selective COX-2 inhibitor NS-398 despite their inhibition on TGF-beta1-induced PGE(2) release. Dexamethasone 175-188 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 10893219-4 2000 Maximal IL-8 release was achieved with 10 ng/ml of TGF-beta1 after 16 h of incubation, which was inhibited by the transcription inhibitor actinomycin D and the corticosteroid dexamethasone but was not affected by the nonselective COX inhibitor indomethacin and the selective COX-2 inhibitor NS-398 despite their inhibition on TGF-beta1-induced PGE(2) release. Indomethacin 244-256 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 10893219-4 2000 Maximal IL-8 release was achieved with 10 ng/ml of TGF-beta1 after 16 h of incubation, which was inhibited by the transcription inhibitor actinomycin D and the corticosteroid dexamethasone but was not affected by the nonselective COX inhibitor indomethacin and the selective COX-2 inhibitor NS-398 despite their inhibition on TGF-beta1-induced PGE(2) release. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 291-297 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 10893219-4 2000 Maximal IL-8 release was achieved with 10 ng/ml of TGF-beta1 after 16 h of incubation, which was inhibited by the transcription inhibitor actinomycin D and the corticosteroid dexamethasone but was not affected by the nonselective COX inhibitor indomethacin and the selective COX-2 inhibitor NS-398 despite their inhibition on TGF-beta1-induced PGE(2) release. Prostaglandins E 344-347 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 10873156-2 2000 Here, we tested the effects of the beta(2)-agonists salbutamol (Salbu) and salmeterol (Salme) on IL-8 release and tumor necrosis factor (TNF)-alpha-induced IL-8 release from ASM cells. Albuterol 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10873156-2 2000 Here, we tested the effects of the beta(2)-agonists salbutamol (Salbu) and salmeterol (Salme) on IL-8 release and tumor necrosis factor (TNF)-alpha-induced IL-8 release from ASM cells. Albuterol 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10873156-2 2000 Here, we tested the effects of the beta(2)-agonists salbutamol (Salbu) and salmeterol (Salme) on IL-8 release and tumor necrosis factor (TNF)-alpha-induced IL-8 release from ASM cells. Salmeterol Xinafoate 75-85 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10873156-2 2000 Here, we tested the effects of the beta(2)-agonists salbutamol (Salbu) and salmeterol (Salme) on IL-8 release and tumor necrosis factor (TNF)-alpha-induced IL-8 release from ASM cells. Salmeterol Xinafoate 87-92 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. Steroids 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. Dexamethasone 81-94 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. Dexamethasone 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10921707-6 2000 RESULTS: In the pilot study, heparin-bonded circuit patients had less complement 3a (p < 0.001) and interleukin-8 (p < 0.05) compared with uncoated cardiopulmonary bypass circuit patients. Heparin 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 103-116 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. Fluticasone 124-135 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. Fluticasone 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. Albuterol 180-185 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. Salmeterol Xinafoate 187-192 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. Colforsin 194-197 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10873156-4 2000 TNF-alpha (10 ng/ml)-induced IL-8 release was markedly inhibited by the steroids dexamethasone (Dex) (0.1 to 10 microM) and fluticasone (Flut) (0.01 to 1 microM) but unaffected by Salbu, Salme, FSK, or 8-Br-cAMP. 8-Bromo Cyclic Adenosine Monophosphate 202-211 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 10873157-5 2000 Expression of IL-6 and IL-8 was sensitive to SB203580, the specific inhibitor of p38 mitogen-activated protein (MAP) kinase and PD98059, an inhibitor of MAP kinase kinase. SB 203580 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 10953284-5 2000 Pretreatment of poorly and highly metastatic human HT-29 colon carcinoma cells with the broad-range inhibitors sodium fluoride (NaF) and sodium pyrophosphate (PyroP) resulted in strong reduction in adhesion of HT-29 cells to various ECM components. Sodium Fluoride 111-126 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 10953284-8 2000 Therefore, the effects of NaF on adhesion-mediated Tyr phosphorylation were investigated further. Tyrosine 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 11357999-4 2000 Both the replication of DV and the production of IL-6 and IL-8 by HUVEC after DV infection were inhibited by ribavirin, an antiviral synthetic guanosine analogue. Ribavirin 109-118 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 11357999-4 2000 Both the replication of DV and the production of IL-6 and IL-8 by HUVEC after DV infection were inhibited by ribavirin, an antiviral synthetic guanosine analogue. Guanosine 143-152 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 10861141-9 2000 However, expression of TNF-alpha and IL-8, IFN-gamma, and IL-6 and IL-1beta was 2-20 times greater in patients administered 100% than in those administered 30% oxygen. Oxygen 160-166 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 10921541-13 2000 CONCLUSIONS: PGE1 suppressed the production of IL-6 and IL-8 but not IL-10, IL-1ra, sTNF RI, or sTNF RII. Alprostadil 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 10808107-9 2000 RESULTS: MEEs from children with chronic mucous otitis media contained significantly higher mean concentrations of IL-8 559.4 pg/mg total protein (TP) (+/-535.6) in comparison with normal serum 17.79 pg/mg TP (+/-10.9), serous OM 40.3 pg/mg TP (+/-28.1) and purulent OM 104.4 pg/mg TP (+/-128.6). tp 147-149 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 10808107-9 2000 RESULTS: MEEs from children with chronic mucous otitis media contained significantly higher mean concentrations of IL-8 559.4 pg/mg total protein (TP) (+/-535.6) in comparison with normal serum 17.79 pg/mg TP (+/-10.9), serous OM 40.3 pg/mg TP (+/-28.1) and purulent OM 104.4 pg/mg TP (+/-128.6). tp 206-208 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 11225832-4 2000 The tolerance limits of electrolytes, NaCl, NaF, NaI, NaNO3, Na2SO4 and of cations, Mg2+ and Ca2+ in the sorption of the six metal ions are reported. Metals 125-130 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 10926336-0 2000 Erythromycin inhibits beta2-integrins (CD11b/CD18) expression, interleukin-8 release and intracellular oxidative metabolism in neutrophils. Erythromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 10882695-2 2000 Grepafloxacin 1-30 mg/L inhibited the production of interleukin 1alpha (IL-1alpha) and IL-1beta, and the expression of IL-1alpha, IL-1beta, tumour necrosis factor alpha (TNFalpha), IL-6 and IL-8 mRNA. grepafloxacin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 10884648-10 2000 In contrast, nitroglycerin infusion significantly increased C3a in patients without diabetes and increased elastase and interleukin 8 levels in patients with diabetes. Nitroglycerin 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 120-133 10864914-6 2000 Treatment of the TC/EC coculture media with anti-TNF-alpha or anti-IL-8 antibodies reduced the media-induced neutrophil adhesion response. Technetium 17-19 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 10875492-2 2000 Interleukin-8 in the sputa from GD-induced asthmatic patients increased significantly after the exposure to GD. Gadolinium 32-34 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 10875492-2 2000 Interleukin-8 in the sputa from GD-induced asthmatic patients increased significantly after the exposure to GD. Gadolinium 108-110 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 10875492-3 2000 OBJECTIVE: To confirm IL-8 production from bronchial epithelial cells when exposed to GD, and to evaluate the role of IL-8 on neutrophil recruitment. Gadolinium 86-88 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 10875492-9 2000 RESULTS: Interleukin-8 production and neutrophil chemotactic activity from bronchial epithelial cells significantly increased with additions of GD in a dose-dependent manner (P < .05, respectively), and were significantly augmented with additions of PBMC supernatant (P < .05, respectively) at each concentration. Gadolinium 144-146 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 10875492-12 2000 CONCLUSION: These results suggest that IL-8 produced from bronchial epithelial cells may be a major cytokine, which induces neutrophil migration into the airways when exposed to GD. Gadolinium 178-180 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 10917872-1 2000 Does inhibition of the mevalonate pathway lower interleukin-8 levels in the vessel wall? Mevalonic Acid 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 10864914-6 2000 Treatment of the TC/EC coculture media with anti-TNF-alpha or anti-IL-8 antibodies reduced the media-induced neutrophil adhesion response. ec 20-22 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 10862535-3 2000 The aim of this study was to determine whether the increased histamine release in highly trained athletes is related to a high plasma level in interleukin-1 beta (IL-1beta), IL-3, or IL-8 in arterial blood. Histamine 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 11108572-5 2000 Among OA patients in whom remarkable improvement was noted in hydrarthrosis, the synovial fluid IL-6 and IL-8 levels at the initial examination were relatively higher, and were markedly decreased after treatment with sodium hyaluronate (NaHA). Hyaluronic Acid 217-235 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 11108572-5 2000 Among OA patients in whom remarkable improvement was noted in hydrarthrosis, the synovial fluid IL-6 and IL-8 levels at the initial examination were relatively higher, and were markedly decreased after treatment with sodium hyaluronate (NaHA). naha 237-241 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 11108572-6 2000 Among those in whom no improvement was noted in hydrarthrosis, the synovial fluid IL-6 and IL-8 levels at the time of initial examination were relatively lower, and hydrarthrosis was not significantly improved even after treatment with NaHA. naha 236-240 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 10837166-4 2000 Treatment of cells with diphenylene iodonium inhibited virus-induced oxidative stress and IL-8 elaboration, but allopurinol, ibuprofen, and rotenone had no effect. diphenyleneiodonium 24-44 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 10875461-10 2000 Oxygen-derived free radicals and many cytokines (e.g., interleukin [IL]-1, IL-6, IL-8, tumor necrosis factor-alpha, platelet activating factor) are considered to be principal mediators in the transformation of acute pancreatitis from a local inflammatory process into a multiorgan illness. Oxygen 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 10957762-8 2000 In cultured respiratory epithelial cells, calcium oxalate increases the release of two interleukins (IL), IL-8 and IL-6, involved in granuloma formation by 8 to 10 fold within 24 hours. Calcium Oxalate 42-57 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 10938902-5 2000 S1P displayed a dual effect on sodium fluoride (NaF)-induced platelet aggregation and had no effect on the aggregation induced by ADP or lysophosphatidic acid (LPA). Sodium Fluoride 31-46 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 10894110-10 2000 Both N-acetylcysteine and pyrrolidine dithiocarbamate attenuated the action of DEP on IL-8 mRNA expression, suggesting that oxidant-mediated pathway might be involved in its processes. Acetylcysteine 5-21 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 10894110-10 2000 Both N-acetylcysteine and pyrrolidine dithiocarbamate attenuated the action of DEP on IL-8 mRNA expression, suggesting that oxidant-mediated pathway might be involved in its processes. pyrrolidine dithiocarbamic acid 26-53 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 10828966-14 2000 Furthermore, the stimulations exerted by GTPgammaS, isoproterenol, FSK, and NaF on adenylyl cyclase were also augmented in cells treated with C-ANP(4-23). c-anp 142-147 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 10807767-3 2000 Using human umbilical vein endothelial cells (HUVECs), we analyzed the role of small GTP-binding Rho proteins and p38 mitogen-activated protein kinase (MAPK) for LPS-dependent IL-8 expression in endothelial cells. Guanosine Triphosphate 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 18967950-7 2000 The effect of NaF, NaCl, NaNO(3), Na(2)SO(4), and Na(3)PO(4) on the sorption of these metal ions has been investigated. Metals 86-91 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 10775461-2 2000 Here, we investigated whether arsenic, which has been shown to inhibit the ubiquitin-proteasome pathway, could inhibit TNF-alpha-mediated increases in IL-8 expression. Arsenic 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 10887619-0 2000 Macrolide treatment decreased the size of nasal polyps and IL-8 levels in nasal lavage. Macrolides 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 10887619-3 2000 Lancet 351:420, 1998), and that macrolides can directly reduce the production of IL-8 by nasal epithelial cells (Suzuki H, Shimomura A, Ikeda K, et al. Macrolides 32-42 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 10887619-7 2000 The IL-8 levels in nasal lavage from patients with nasal polyps were reduced during macrolide treatment. Macrolides 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 10887619-9 2000 In the group whose polyps were reduced in size, the IL-8 levels dramatically decreased from 231.2 pg/mL to 44.0 pg/mL (p < 0.05), and were significantly higher before macrolide treatment than those in the group whose polyps showed no change (p < 0.005). Macrolides 170-179 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 10887619-10 2000 This reduction in IL-8 may be an important aspect of the effect of macrolide treatment on nasal polyps in chronic rhinosinusitis. Macrolides 67-76 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 10770757-3 2000 In this study, AG7088 was tested for its antiviral activity and ability to inhibit the production of IL-6 and IL-8 in a human bronchial epithelial cell line, BEAS-2B. rupintrivir 15-21 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 10770757-5 2000 Treatment of HRV 14-infected cells with AG7088 resulted in a statistically significant (P, <0.05) dose-dependent reduction in the levels of infectious virus as well as IL-6 and IL-8 released into the cell supernatant compared to the results obtained for compound-free infected cells. rupintrivir 40-46 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 10817569-0 2000 Extracellular signal-regulated kinase 1/extracellular signal-regulated kinase 2 mitogen-activated protein kinase signaling and activation of activator protein 1 and nuclear factor kappaB transcription factors play central roles in interleukin-8 expression stimulated by monosodium urate monohydrate and calcium pyrophosphate crystals in monocytic cells. Uric Acid 270-298 C-X-C motif chemokine ligand 8 Homo sapiens 231-244 10770757-7 2000 In time-of-addition studies, AG7088 could be added as late as 14 to 26 h after HRV 14 infection of BEAS-2B cells and still result in a statistically significant (P, <0.05) reduction in the levels of infectious virus, IL-6, and IL-8 compared to the results obtained for compound-free infected cells. rupintrivir 29-35 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 10775461-6 2000 Exposing the cells to 500 microM arsenite, prior to adding TNF-alpha, completely inhibited IkappaBalpha degradation, NF-kappaB translocation, NF-kappaB-dependent gene transcription, and transcription of the endogenous gene for IL-8. arsenite 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 227-231 10817569-0 2000 Extracellular signal-regulated kinase 1/extracellular signal-regulated kinase 2 mitogen-activated protein kinase signaling and activation of activator protein 1 and nuclear factor kappaB transcription factors play central roles in interleukin-8 expression stimulated by monosodium urate monohydrate and calcium pyrophosphate crystals in monocytic cells. Calcium Pyrophosphate 303-324 C-X-C motif chemokine ligand 8 Homo sapiens 231-244 10823417-4 2000 In this report, we demonstrate that a subset of human lung carcinoma cell lines respond to paclitaxel treatment with an up to a fivefold increase in the production of interleukin-8 (IL-8). Paclitaxel 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 10823417-0 2000 Paclitaxel up-regulates interleukin-8 synthesis in human lung carcinoma through an NF-kappaB- and AP-1-dependent mechanism. Paclitaxel 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 10823417-6 2000 Increased IL-8 mRNA is seen as early as 45 min with a peak at 4 h after paclitaxel treatment. Paclitaxel 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 10823417-4 2000 In this report, we demonstrate that a subset of human lung carcinoma cell lines respond to paclitaxel treatment with an up to a fivefold increase in the production of interleukin-8 (IL-8). Paclitaxel 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 167-180 10773004-7 2000 The results showed that LPS induced p38 MAP kinase phosphorylation and activity, and SB 203580 as a selective inhibitor of p38 MAP kinase activity inhibited p38 MAP kinase activity and IL-8 expression in LPS-stimulated pulmonary vascular endothelial cells. SB 203580 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 11515628-6 2000 RESULTS: Incubation of neutrophils with 10(-6) to 10(4) M troxipide caused inhibition of recombinant interleukin-8-induced migration. troxipide 58-67 C-X-C motif chemokine ligand 8 Homo sapiens 101-114 10843593-0 2000 Polyoxygenated dysidea sterols that inhibit the binding of [I125] IL-8 to the human recombinant IL-8 receptor type A. Sterols 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 10815919-11 2000 Similarly after 11 days treatment, production of vascular endothelial growth factor and interleukin 8 was significantly lower in C225 and C225 plus gemcitabine-treated tumors versus gemcitabine-treated and control tumors. gemcitabine 148-159 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 10815919-11 2000 Similarly after 11 days treatment, production of vascular endothelial growth factor and interleukin 8 was significantly lower in C225 and C225 plus gemcitabine-treated tumors versus gemcitabine-treated and control tumors. gemcitabine 182-193 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 10853849-2 2000 Recent research shows that macrolide antibiotics may reduce interleukin (IL)-8 production by bronchial epithelial cells and inhibit neutrophil chemotaxis. macrolide antibiotics 27-48 C-X-C motif chemokine ligand 8 Homo sapiens 60-78 10853849-6 2000 There were significant (p<0.05) pre- to post-exposure increases in total cells, neutrophils, IL-6 and IL-8 in both the azithromycin and placebo arms. Azithromycin 122-134 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 10843593-0 2000 Polyoxygenated dysidea sterols that inhibit the binding of [I125] IL-8 to the human recombinant IL-8 receptor type A. Sterols 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 10833370-9 2000 Levels of IL-8 mRNA and protein were also dose-dependently increased by stimulation with IL-1beta, TNF-alpha and TPA. Tetradecanoylphorbol Acetate 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 10843593-1 2000 The combined CH(2)Cl(2) and MeOH crude extract of a new species of the marine sponge Dysidea, collected in Northern Australia was found to inhibit the binding of [I125] interleukin-8 [IL-8] to the human recombinant IL-8 receptor type A at 500 microg/mL. (2)cl 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 10843593-1 2000 The combined CH(2)Cl(2) and MeOH crude extract of a new species of the marine sponge Dysidea, collected in Northern Australia was found to inhibit the binding of [I125] interleukin-8 [IL-8] to the human recombinant IL-8 receptor type A at 500 microg/mL. (2)cl 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 10843593-1 2000 The combined CH(2)Cl(2) and MeOH crude extract of a new species of the marine sponge Dysidea, collected in Northern Australia was found to inhibit the binding of [I125] interleukin-8 [IL-8] to the human recombinant IL-8 receptor type A at 500 microg/mL. (2)cl 15-20 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 10843593-1 2000 The combined CH(2)Cl(2) and MeOH crude extract of a new species of the marine sponge Dysidea, collected in Northern Australia was found to inhibit the binding of [I125] interleukin-8 [IL-8] to the human recombinant IL-8 receptor type A at 500 microg/mL. Methanol 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 169-182 10843593-1 2000 The combined CH(2)Cl(2) and MeOH crude extract of a new species of the marine sponge Dysidea, collected in Northern Australia was found to inhibit the binding of [I125] interleukin-8 [IL-8] to the human recombinant IL-8 receptor type A at 500 microg/mL. Methanol 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 10843593-1 2000 The combined CH(2)Cl(2) and MeOH crude extract of a new species of the marine sponge Dysidea, collected in Northern Australia was found to inhibit the binding of [I125] interleukin-8 [IL-8] to the human recombinant IL-8 receptor type A at 500 microg/mL. Methanol 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 10921280-6 2000 Acute exposure to cigarette smoke initiates a superoxide-dependent mechanism that, through NF-kappa B activation and IL-8 expression, induces infiltration of neutrophils into the airways in vivo. Superoxides 46-56 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 11778222-7 2000 After dexamethasone treatment, the expression of NF-kappa B activation and IL-8 mRNA became lower. Dexamethasone 6-19 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 10868450-7 2000 In patients with DU the duodenal mucosal tissues with GM (MB-unstained mucosa) showed significantly higher levels of IL-8 than those without GM (MB-stained mucosa) or the antral mucosa. gm 54-56 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 10868450-10 2000 CONCLUSIONS: Increased IL-8 activity in the duodenal mucosa with GM may be important for ulcerogenesis in H. pylori-positive DU patients. gm 65-67 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 10886812-7 2000 The concurrent application of indomethacin at 10 microg/ml reversed this interleukin-8 induced inhibition. Indomethacin 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 10784148-5 2000 NaF gave the best recovery, 104%, for BA relative to the 88% obtained by batch processing. Benzoic Acid 38-40 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 10766857-3 2000 We report that IL-8 mRNA accumulation and protein secretion were down-regulated in IL-1beta- and lipopolysaccharide-stimulated differentiated HT-29 cells (HT-29/MTX, where MTX is methotrexate) compared with undifferentiated cells (HT-29/p), whereas no differential effects were found following tumor necrosis factor (TNF)-alpha or phorbol myristate acetate stimulation. Methotrexate 161-164 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 10766857-3 2000 We report that IL-8 mRNA accumulation and protein secretion were down-regulated in IL-1beta- and lipopolysaccharide-stimulated differentiated HT-29 cells (HT-29/MTX, where MTX is methotrexate) compared with undifferentiated cells (HT-29/p), whereas no differential effects were found following tumor necrosis factor (TNF)-alpha or phorbol myristate acetate stimulation. Methotrexate 172-175 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 10766857-3 2000 We report that IL-8 mRNA accumulation and protein secretion were down-regulated in IL-1beta- and lipopolysaccharide-stimulated differentiated HT-29 cells (HT-29/MTX, where MTX is methotrexate) compared with undifferentiated cells (HT-29/p), whereas no differential effects were found following tumor necrosis factor (TNF)-alpha or phorbol myristate acetate stimulation. Methotrexate 179-191 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 10766857-3 2000 We report that IL-8 mRNA accumulation and protein secretion were down-regulated in IL-1beta- and lipopolysaccharide-stimulated differentiated HT-29 cells (HT-29/MTX, where MTX is methotrexate) compared with undifferentiated cells (HT-29/p), whereas no differential effects were found following tumor necrosis factor (TNF)-alpha or phorbol myristate acetate stimulation. Tetradecanoylphorbol Acetate 331-356 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 10769273-12 2000 Coincubation with cerivastatin resulted in significantly lower MCP-1 and IL-8 production, whereas the release of TNF-alpha remained unaffected. cerivastatin 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 10754327-13 2000 LY294002 blocked IL-8-dependent Akt phosphorylation. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 10754327-14 2000 PD98059 and LY294002 significantly attenuated IL-8 delay of apoptosis. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 10754327-14 2000 PD98059 and LY294002 significantly attenuated IL-8 delay of apoptosis. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 10722601-8 2000 The release of interleukin-8 was markedly suppressed by the p38 mitogen-activated protein kinase inhibitor SB203580 but was only minimally suppressed by the mitogen-activated protein/extracellular signal-regulated kinase inhibitor PD98059. SB 203580 107-115 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 10753876-0 2000 Reactive nitrogen and oxygen species attenuate interleukin- 8-induced neutrophil chemotactic activity in vitro. reactive nitrogen and oxygen species 0-36 C-X-C motif chemokine ligand 8 Homo sapiens 47-61 10753876-3 2000 To test this hypothesis, the neutrophil chemotactic activity (NCA) of interleukin-8 (IL-8) incubated with peroxynitrite was evaluated. Peroxynitrous Acid 106-119 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 10753876-3 2000 To test this hypothesis, the neutrophil chemotactic activity (NCA) of interleukin-8 (IL-8) incubated with peroxynitrite was evaluated. Peroxynitrous Acid 106-119 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 10753876-4 2000 Peroxynitrite attenuated IL-8 NCA in a dose-dependent manner (p < 0.01) but did not significantly reduce NCA induced by leukotriene B(4) or complement-activated serum. Peroxynitrous Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 10753876-6 2000 Papa-NONOate [N-(3-ammoniopropyl)-N-(n-propyl)amino]diazen-1-ium-1, 2-dialase or sodium nitroprusside, NO donors, or a combination of xanthine and xanthine oxidase to generate superoxide did not show an inhibitory effect on NCA induced by IL-8. PAPA NONOate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 10753876-6 2000 Papa-NONOate [N-(3-ammoniopropyl)-N-(n-propyl)amino]diazen-1-ium-1, 2-dialase or sodium nitroprusside, NO donors, or a combination of xanthine and xanthine oxidase to generate superoxide did not show an inhibitory effect on NCA induced by IL-8. -ium 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 10753876-7 2000 In contrast, small amounts of SIN-1, a peroxynitrite generator, caused a concentration-dependent inhibition of NCA by IL-8. Peroxynitrous Acid 39-52 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 10753876-8 2000 Consistent with its capacity to reduce NCA, peroxynitrite treatment reduced IL-8 binding to neutrophils. Peroxynitrous Acid 44-57 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 10798763-6 2000 FK506 and MMF were also able to upregulate IL-8, although the effect was less dramatic than observed for CsA. Tacrolimus 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 10798763-7 2000 Low concentrations of prednisolone (0.01 and 0.001 microg/ml) enhanced IL-6 and IL-8 secretion, whereas concentrations > or =0.01 microg/ml significantly diminished IL-6 secretion. Prednisolone 22-34 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 10807428-6 2000 In vitro sofalcone has a significant bacteriocidal effect against H. pylori and can also significantly prevent adherence of this bacterium to MKN45 cells, thus remarkably reducing IL-8 production of these cells in response to stimulation by H. pylori. sofalcone 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 10809292-0 2000 Perfluorocarbon blocks tumor necrosis factor-alpha-induced interleukin-8 release from alveolar epithelial cells in vitro. Fluorocarbons 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 10809292-1 2000 OBJECTIVE: To determine whether tumor necrosis factor (TNF)-alpha-induced interleukin (IL)-8 production by pulmonary alveolar epithelial cells is blocked by perfluorocarbon (PFC). Fluorocarbons 157-172 C-X-C motif chemokine ligand 8 Homo sapiens 74-92 10772385-9 2000 At the mRNA level, inhibition was only seen with KU812 cells and IL-8 in the presence of azelastine at 10-(10) M. These data show thus distinct inhibitory patterns for different antihistamines during cytokine production from human mast cells and basophils which may contribute to the anti-inflammatory effects of these drugs during treatment of allergic diseases. azelastine 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 10753876-9 2000 Nitrotyrosine was detected in the IL-8 incubated with peroxynitrite by enzyme-linked immunosorbent assay. 3-nitrotyrosine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 10753876-9 2000 Nitrotyrosine was detected in the IL-8 incubated with peroxynitrite by enzyme-linked immunosorbent assay. Peroxynitrous Acid 54-67 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 10753876-10 2000 These findings are consistent with nitration of tyrosine by peroxynitrite with subsequent inhibition of IL-8 binding to neutrophils and a reduction in NCA and suggest that oxidants may play an important role in regulation of IL-8-induced neutrophil chemotaxis. Tyrosine 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 10753876-10 2000 These findings are consistent with nitration of tyrosine by peroxynitrite with subsequent inhibition of IL-8 binding to neutrophils and a reduction in NCA and suggest that oxidants may play an important role in regulation of IL-8-induced neutrophil chemotaxis. Tyrosine 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 10753876-10 2000 These findings are consistent with nitration of tyrosine by peroxynitrite with subsequent inhibition of IL-8 binding to neutrophils and a reduction in NCA and suggest that oxidants may play an important role in regulation of IL-8-induced neutrophil chemotaxis. Peroxynitrous Acid 60-73 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 10753876-10 2000 These findings are consistent with nitration of tyrosine by peroxynitrite with subsequent inhibition of IL-8 binding to neutrophils and a reduction in NCA and suggest that oxidants may play an important role in regulation of IL-8-induced neutrophil chemotaxis. Peroxynitrous Acid 60-73 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 10745031-0 2000 A novel mechanism of retinoic acid-enhanced interleukin-8 gene expression in airway epithelium. Tretinoin 21-34 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 10745031-1 2000 A 3- to 8-fold stimulation of interleukin (IL)-8 gene expression by all-trans-retinoic acid (ATRA) was demonstrated in primary cultures of human and monkey tracheobronchial epithelial cells and BEAS-2B serum-sensitive cell line. Tretinoin 71-91 C-X-C motif chemokine ligand 8 Homo sapiens 30-48 10745031-1 2000 A 3- to 8-fold stimulation of interleukin (IL)-8 gene expression by all-trans-retinoic acid (ATRA) was demonstrated in primary cultures of human and monkey tracheobronchial epithelial cells and BEAS-2B serum-sensitive cell line. Tretinoin 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 30-48 10745031-2 2000 The effect of ATRA on IL-8 gene expression is dose- and time-dependent. Tretinoin 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 10745031-5 2000 A difference in nuclear run-on activity suggests that a transcriptional mechanism is involved in ATRA-enhanced IL-8 gene expression. Tretinoin 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 10745031-13 2000 Taking these data together, a novel mechanism is proposed in which ATRA activates promoter activity of IL-8 gene through TRX-dependent NF-kappaB activation. Tretinoin 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 10805216-5 2000 IFN-gamma as well as the GCs, Dexamethasone and Budesonide, inhibited TNF-alpha induced IL-8 secretion in a dose-dependent manner. Dexamethasone 30-43 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 10805216-5 2000 IFN-gamma as well as the GCs, Dexamethasone and Budesonide, inhibited TNF-alpha induced IL-8 secretion in a dose-dependent manner. Budesonide 48-58 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 10744650-7 2000 Cap formation and superoxide anion production induced by solid-phase P-selectin or by IL-8 and soluble rP-selectin treatment were inhibited by treatment of the leukocytes with cytochalasin B. Superoxides 18-34 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 10722601-8 2000 The release of interleukin-8 was markedly suppressed by the p38 mitogen-activated protein kinase inhibitor SB203580 but was only minimally suppressed by the mitogen-activated protein/extracellular signal-regulated kinase inhibitor PD98059. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 231-238 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 10805370-8 2000 The enhancement of IL-6 and IL-8 production by MCG was abrogated when MCG were pretreated with the serine protease inhibitor phenylmethylsulfonyl fluoride (PMSF). Phenylmethylsulfonyl Fluoride 125-154 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 10760560-5 2000 RESULTS: Moclobemide 10(-3) and 10(-5) M significantly suppressed the unstimulated production of TNFalpha and IL-8, and significantly enhanced the stimulated-production of IL-10. Moclobemide 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 10760560-7 2000 CONCLUSIONS: Moclobemide has negative immunoregulatory capacities through inhibition of the production of proinflammatory cytokines, i.e. TNFalpha and IL-8, and through enhancement of the production of IL-10, an anti-inflammatory cytokine. Moclobemide 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 10782906-11 2000 During steroid therapy, plasma levels of the pro-inflammatory cytokine IL-8 fell as early as day 14, while levels of the anti-inflammatory cytokine IL-10 increased on day 21. Steroids 7-14 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 10725748-7 2000 In the same cells, IL-8 also caused superoxide release. Superoxides 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 10805370-8 2000 The enhancement of IL-6 and IL-8 production by MCG was abrogated when MCG were pretreated with the serine protease inhibitor phenylmethylsulfonyl fluoride (PMSF). Phenylmethylsulfonyl Fluoride 156-160 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 10677576-0 2000 Attenuation of interleukin-8 production by inhibiting nuclear factor-kappaB translocation using decoy oligonucleotides. Oligonucleotides 102-118 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 10865191-3 2000 Arabinosylated lipoarabinomannan (ARA-LAM) stimulated hyporesponsiveness by reducing TNF-alpha, GM-CSF, G-CSF, IL-10, and IL-6 release similarly to LPS, but caused no changes in IL-8 secretion. lipoarabinomannan 15-32 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 10865191-3 2000 Arabinosylated lipoarabinomannan (ARA-LAM) stimulated hyporesponsiveness by reducing TNF-alpha, GM-CSF, G-CSF, IL-10, and IL-6 release similarly to LPS, but caused no changes in IL-8 secretion. ara-lam 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 10775070-1 2000 We have previously shown that the in vivo infusion of interleukin-8 (IL8) in rats causes albuminuria and an increased catabolism of the heparan sulfate (HS) glycosaminoglycans (GAG). Heparitin Sulfate 136-151 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 10775070-1 2000 We have previously shown that the in vivo infusion of interleukin-8 (IL8) in rats causes albuminuria and an increased catabolism of the heparan sulfate (HS) glycosaminoglycans (GAG). hs) glycosaminoglycans 153-175 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 10775070-1 2000 We have previously shown that the in vivo infusion of interleukin-8 (IL8) in rats causes albuminuria and an increased catabolism of the heparan sulfate (HS) glycosaminoglycans (GAG). Glycosaminoglycans 177-180 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 10775070-6 2000 The HSGAG 35sulfate uptake was higher in IL8-treated rats than controls (387+/-138 vs. 246+/-15 cpm/1,000 glomeruli, mean +/- SD, P<0.05). 35sulfate 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 10722953-0 2000 Modulating pharmacokinetics of an anti-interleukin-8 F(ab")(2) by amine-specific PEGylation with preserved bioactivity. Amines 66-71 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 10677576-5 2000 In the current study, we produced phosphorothioate-modified oligonucleotides containing the specific DNA sequence that NF-kappaB binds within the IL-8 gene. Parathion 34-50 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 10677576-5 2000 In the current study, we produced phosphorothioate-modified oligonucleotides containing the specific DNA sequence that NF-kappaB binds within the IL-8 gene. Oligonucleotides 60-76 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 10677576-7 2000 We found that transfection with these oligonucleotides significantly inhibited monocyte IL-8 production. Oligonucleotides 38-54 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 10677576-9 2000 This single-stranded oligonucleotide also inhibited IL-1beta-induced translocation of NF-kappaB to the nucleus and reduced IL-8 mRNA expression. Oligonucleotides 21-36 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 10677576-10 2000 These studies demonstrated that monocyte production of IL-8 can be attenuated using a single-stranded oligonucleotide that binds a transcriptional activating protein before it translocates to the cell nucleus. single-stranded oligonucleotide 86-117 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 10706733-4 2000 Exposure of non-CF gland cells to hypotonic (85 mM) NaCl solution, compared with isotonic (115 mM) NaCl and hypertonic (170 mM) NaCl solutions, resulted in a significant decrease in IL-8 production that was paralleled by a strong inhibition of activated NF-kappa B associated with an increased cytosolic expression of I kappa B alpha and a decrease in the I kappa B kinase alpha protein level. Sodium Chloride 52-56 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 10706733-7 2000 This is the first demonstration that primary human CF bronchial gland cells exhibit abnormally high IL-8 production through constitutively activated NF-kappa B and high I kappa B kinase alpha level, whatever the hypo-, iso-, and hypertonic NaCl milieu. Sodium Chloride 240-244 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 10706733-0 2000 High susceptibility for cystic fibrosis human airway gland cells to produce IL-8 through the I kappa B kinase alpha pathway in response to extracellular NaCl content. Sodium Chloride 153-157 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 10702246-6 2000 Treatment of SK-OV-3 cells with the inhibitors genestein and herbimycin A indicated that tyrosine kinases were involved in the IL-8 activation of Erk1 and Erk2. herbimycin 61-73 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 10706733-4 2000 Exposure of non-CF gland cells to hypotonic (85 mM) NaCl solution, compared with isotonic (115 mM) NaCl and hypertonic (170 mM) NaCl solutions, resulted in a significant decrease in IL-8 production that was paralleled by a strong inhibition of activated NF-kappa B associated with an increased cytosolic expression of I kappa B alpha and a decrease in the I kappa B kinase alpha protein level. nacl solution 52-65 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 10755555-0 2000 Association of glucocorticoids and cyclosporin A or rapamycin prevents E-selectin and IL-8 expression during LPS- and TNFalpha-mediated endothelial cell activation. Cyclosporine 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 10755555-0 2000 Association of glucocorticoids and cyclosporin A or rapamycin prevents E-selectin and IL-8 expression during LPS- and TNFalpha-mediated endothelial cell activation. Sirolimus 52-61 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. Sesquiterpenes 126-139 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 10696066-7 2000 Antioxidants, pyrrolidine dithiocarbamate, and N-acetyl-L-cysteine significantly inhibited IL-8 mRNA and protein levels by BET-1A cells. pyrrolidine dithiocarbamic acid 14-41 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 10696066-7 2000 Antioxidants, pyrrolidine dithiocarbamate, and N-acetyl-L-cysteine significantly inhibited IL-8 mRNA and protein levels by BET-1A cells. Acetylcysteine 47-66 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 10725111-7 2000 The removal of the glass-phase iron greatly reduced the amount of iron that could be mobilized by citrate and prevented the particles from inducing interleukin-8 in cultured human lung epithelial (A549) cells. Iron 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 10725111-7 2000 The removal of the glass-phase iron greatly reduced the amount of iron that could be mobilized by citrate and prevented the particles from inducing interleukin-8 in cultured human lung epithelial (A549) cells. Iron 66-70 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 10702362-0 2000 Cadmium-induced acute hepatic injury is exacerbated in human interleukin-8 transgenic mice. Cadmium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 10704251-0 2000 Sesquiterpene lactones are potent inhibitors of interleukin 8 gene expression in cultured human respiratory epithelium. sesquiterpene lactones 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. Sesquiterpenes 126-139 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. Sesquiterpenes 126-139 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. Lactones 140-148 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. Lactones 140-148 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. Lactones 140-148 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. isohelenin 150-160 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. isohelenin 150-160 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. parthenolide 165-177 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. parthenolide 165-177 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 10704251-3 2000 Because activation of NF-kappaB is involved in the regulation of the chemokine interleukin 8 (IL-8), we hypothesized that the sesquiterpene lactones, isohelenin and parthenolide, would inhibit IL-8 gene expression in cultured human respiratory epithelium. parthenolide 165-177 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 10704251-5 2000 Pretreatment with either isohelenin or parthenolide inhibited TNF-alpha-mediated IL-8 gene expression in a concentration-dependent manner. isohelenin 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 10704251-5 2000 Pretreatment with either isohelenin or parthenolide inhibited TNF-alpha-mediated IL-8 gene expression in a concentration-dependent manner. parthenolide 39-51 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 10704251-8 2000 We conclude that sesquiterpene lactones are potent in vitro inhibitors of IL-8 gene expression in cultured human respiratory epithelium. sesquiterpene lactones 17-39 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 10704251-11 2000 The ability of sesquiterpene lactones to modulate IL-8 gene expression may explain, in part, their anti-inflammatory effects. sesquiterpene lactones 15-37 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 10759440-9 2000 However, MTX treatment was associated with a significant fall in serum levels of free IL-8 (p=0.03). Methotrexate 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 10698971-9 2000 Oxidative stress (decrease of glutathione by 50%) reduced post-TNF-alpha levels of IL-6 to 14 +/- 3 and IL-8 to 1 +/- 0.2; the rise of ICAM-1 was completely blocked and E-selectin was only doubled. Glutathione 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 10679106-0 2000 Lipoxin A4 inhibits IL-1 beta-induced IL-6, IL-8, and matrix metalloproteinase-3 production in human synovial fibroblasts and enhances synthesis of tissue inhibitors of metalloproteinases. lipoxin A4 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 10679106-6 2000 At nanomolar concentrations, LXA4 inhibited these IL-1 beta responses with reduction of IL-6 and IL-8 synthesis, by 45 +/- 7% and 75 +/- 11%, respectively, and prevented IL-1 beta-induced MMP-3 synthesis without significantly affecting MMP-1 levels. lipoxin A4 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10630964-0 2000 The antisense oligonucleotide ISIS 2922 prevents cytomegalovirus-induced upregulation of IL-8 and ICAM-1 in cultured human fibroblasts. Oligonucleotides 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 10711865-6 2000 Hydrocortisone (0.05 micromol/L to 50 micromol/L) inhibited cytokine release in a dose-dependent manner with ED50 values of 0.23 micromol/L, 0.19 micromol/L, and 0.10 micromol/L for IL-6, IL-8, and TNF-alpha, respectively. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 10679119-2 2000 Our laboratory has shown that paclitaxel induces IL-8, a member of the C-X-C family of chemokines, in subsets of human ovarian cancer cells. Paclitaxel 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 10630964-0 2000 The antisense oligonucleotide ISIS 2922 prevents cytomegalovirus-induced upregulation of IL-8 and ICAM-1 in cultured human fibroblasts. fomivirsen 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 10846348-0 2000 Interleukin-8 secretion by cultured oral epidermoid carcinoma cells induced with nicotine and/or arecoline treatments. Nicotine 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 10846348-0 2000 Interleukin-8 secretion by cultured oral epidermoid carcinoma cells induced with nicotine and/or arecoline treatments. Arecoline 97-106 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 10846348-7 2000 Nicotine and arecoline, single or combined treatment, increased IL-8 secretion in KB CCL17 cells. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 10846348-7 2000 Nicotine and arecoline, single or combined treatment, increased IL-8 secretion in KB CCL17 cells. Arecoline 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 10656319-4 2000 NaF (1.3% by weight in the mixed cement) was added to the powder components of a glass ionomer based on LG30 glass (which contains Al, Si, Ca, P, and O only). Silicon 135-137 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 10707023-1 2000 The "ELR" (Glu-Leu-Arg) tripeptide sequence near the N-terminus of interleukin-8 (IL-8) contributes a large part of the receptor binding free energy. Glutamic Acid 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 10707023-1 2000 The "ELR" (Glu-Leu-Arg) tripeptide sequence near the N-terminus of interleukin-8 (IL-8) contributes a large part of the receptor binding free energy. Glutamic Acid 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 10707023-1 2000 The "ELR" (Glu-Leu-Arg) tripeptide sequence near the N-terminus of interleukin-8 (IL-8) contributes a large part of the receptor binding free energy. Leucine 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 10707023-1 2000 The "ELR" (Glu-Leu-Arg) tripeptide sequence near the N-terminus of interleukin-8 (IL-8) contributes a large part of the receptor binding free energy. Leucine 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 10707023-1 2000 The "ELR" (Glu-Leu-Arg) tripeptide sequence near the N-terminus of interleukin-8 (IL-8) contributes a large part of the receptor binding free energy. Arginine 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 10707023-1 2000 The "ELR" (Glu-Leu-Arg) tripeptide sequence near the N-terminus of interleukin-8 (IL-8) contributes a large part of the receptor binding free energy. Arginine 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 10707023-1 2000 The "ELR" (Glu-Leu-Arg) tripeptide sequence near the N-terminus of interleukin-8 (IL-8) contributes a large part of the receptor binding free energy. tripeptide K-26 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 10707023-1 2000 The "ELR" (Glu-Leu-Arg) tripeptide sequence near the N-terminus of interleukin-8 (IL-8) contributes a large part of the receptor binding free energy. tripeptide K-26 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 10644044-0 2000 Inhibition of interleukin-8-activated human neutrophil chemotaxis by thapsigargin in a calcium- and cyclic AMP-dependent way. Thapsigargin 69-81 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 10644044-0 2000 Inhibition of interleukin-8-activated human neutrophil chemotaxis by thapsigargin in a calcium- and cyclic AMP-dependent way. Calcium 87-94 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 10644044-0 2000 Inhibition of interleukin-8-activated human neutrophil chemotaxis by thapsigargin in a calcium- and cyclic AMP-dependent way. Cyclic AMP 100-110 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 10644044-1 2000 Chemotactic migration of human neutrophils, induced by interleukin-8 (IL-8) or other activators, was inhibited by thapsigargin in the high nanomolar range. Thapsigargin 114-126 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 10644044-1 2000 Chemotactic migration of human neutrophils, induced by interleukin-8 (IL-8) or other activators, was inhibited by thapsigargin in the high nanomolar range. Thapsigargin 114-126 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 10644044-3 2000 Other inhibitors of Ca(2+)-ATPases associated with intracellular calcium stores, such as cyclopiazonic acid and 2,5-di-(tert-butyl)-1,4-benzohydroquinone, equally inhibited IL-8-activated migration. cyclopiazonic acid 89-107 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 10644044-3 2000 Other inhibitors of Ca(2+)-ATPases associated with intracellular calcium stores, such as cyclopiazonic acid and 2,5-di-(tert-butyl)-1,4-benzohydroquinone, equally inhibited IL-8-activated migration. 2,5-di-tert-butylhydroquinone 112-153 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 10644044-8 2000 Cyclic AMP (cAMP; adenosine 3",5"-cyclic monophosphate) is probably involved in this process, because thapsigargin increased the cAMP level and cAMP inhibited IL-8-activated migration in a calcium-dependent way. Cyclic AMP 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 10644044-8 2000 Cyclic AMP (cAMP; adenosine 3",5"-cyclic monophosphate) is probably involved in this process, because thapsigargin increased the cAMP level and cAMP inhibited IL-8-activated migration in a calcium-dependent way. Cyclic AMP 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 10644044-8 2000 Cyclic AMP (cAMP; adenosine 3",5"-cyclic monophosphate) is probably involved in this process, because thapsigargin increased the cAMP level and cAMP inhibited IL-8-activated migration in a calcium-dependent way. Cyclic AMP 18-54 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 10644044-8 2000 Cyclic AMP (cAMP; adenosine 3",5"-cyclic monophosphate) is probably involved in this process, because thapsigargin increased the cAMP level and cAMP inhibited IL-8-activated migration in a calcium-dependent way. Thapsigargin 102-114 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 10644044-8 2000 Cyclic AMP (cAMP; adenosine 3",5"-cyclic monophosphate) is probably involved in this process, because thapsigargin increased the cAMP level and cAMP inhibited IL-8-activated migration in a calcium-dependent way. Calcium 189-196 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 10656319-4 2000 NaF (1.3% by weight in the mixed cement) was added to the powder components of a glass ionomer based on LG30 glass (which contains Al, Si, Ca, P, and O only). lg30 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 10656319-4 2000 NaF (1.3% by weight in the mixed cement) was added to the powder components of a glass ionomer based on LG30 glass (which contains Al, Si, Ca, P, and O only). Aluminum 131-133 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 10855853-0 2000 In vitro interleukin-8 production by monocytes treated with lithium chloride from breast cancer patients. Lithium Chloride 60-76 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 10855853-1 2000 AIMS AND BACKGROUND: Since interleukin-8 (IL-8) has a suppressive effect on hematopoiesis, lithium induces leukocytosis and granulocytosis and mononuclear cells are defective in patients affected by neoplastic disease, we analyzed IL-8 production by monocytes obtained from patients with nonmetastatic breast cancer (BCaM0) and metastatic breast cancer (BCaM1) and the effect of lithium chloride (LiCl) on these cells. Lithium 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 231-235 10855853-3 2000 Lithium influences the hematopoietic system, which is known to be regulated by numerous cytokines including IL-8. Lithium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 10855853-5 2000 IL-8 release was assessed in supernatants of lipopolysaccharide (LPS) and/or LiCl-treated monocyte cultures. Lithium Chloride 77-81 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10855853-7 2000 In vitro LiCl treatment reduced IL-8 production by monocytes obtained from all subjects compared to the same cells when untreated or LPS treated. Lithium Chloride 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 10855853-8 2000 The suppressive effect of LiCl on IL-8 production by monocytes from breast cancer patients was particularly marked in monocytes from BCaM0 with respect to those from BCaM1. Lithium Chloride 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 10855853-10 2000 Moreover, combined LPS/LiCl treatment of monocytes significantly (p <0.0001) downregulated the release of IL-8 compared to treatment with LPS alone. Lithium Chloride 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10855853-12 2000 Lithium was able to downregulate IL-8 production by monocytes from different subgroups. Lithium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 10657941-8 2000 In contrast to AMs, MO adhesion or exposure to ROFA particles in suspension rapidly activated p38, JNK, and ERK/MAPK, and activated NF-kappaB binding as well as IL-8 mRNA expression. rofa 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 10656319-4 2000 NaF (1.3% by weight in the mixed cement) was added to the powder components of a glass ionomer based on LG30 glass (which contains Al, Si, Ca, P, and O only). Phosphorus 143-144 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 10656319-16 2000 Fluoride addition to a F-free glass ionomer renders it vulnerable to surface disruption by NaF solution showing that fluoride complexes produced in glass dissolution are not necessarily involved in this process. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 91-94 10656319-17 2000 Sodium addition to a Na-free glass ionomer confirms the role of this cement in enhancing pH change in NaF solution. Sodium 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 10688536-2 2000 We tested the hypothesis that iron present in coal fly ash (CFA) could induce the expression and synthesis of the inflammatory cytokine interleukin-8 (IL-8). Iron 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 136-149 10653823-6 2000 Preexposure of ECs for 18 hours with laminar shear stress (15 dyne/cm(2)) abrogated CS-induced IL-8 release to 106+/-10% (P<0.001) and reduced CS-induced MCP-1 expression (170+/-31%; P<0.05). Cesium 84-86 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 10653823-9 2000 Specific inhibition of clusterin by transfection with antisense oligonucleotides reversed the protective effect of shear stress on CS-induced MCP-1 and IL-8 upregulation (P<0.05 versus sense-transfected cells). Oligonucleotides 64-80 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 10653823-9 2000 Specific inhibition of clusterin by transfection with antisense oligonucleotides reversed the protective effect of shear stress on CS-induced MCP-1 and IL-8 upregulation (P<0.05 versus sense-transfected cells). Cesium 131-133 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 10688536-0 2000 Interleukin-8 levels in human lung epithelial cells are increased in response to coal fly ash and vary with the bioavailability of iron, as a function of particle size and source of coal. Iron 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 10688536-2 2000 We tested the hypothesis that iron present in coal fly ash (CFA) could induce the expression and synthesis of the inflammatory cytokine interleukin-8 (IL-8). Iron 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 10688536-2 2000 We tested the hypothesis that iron present in coal fly ash (CFA) could induce the expression and synthesis of the inflammatory cytokine interleukin-8 (IL-8). 3-chloro-4-fluoroaniline 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 136-149 10688536-2 2000 We tested the hypothesis that iron present in coal fly ash (CFA) could induce the expression and synthesis of the inflammatory cytokine interleukin-8 (IL-8). 3-chloro-4-fluoroaniline 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 10688536-5 2000 Treatment of human lung epithelial (A549) cells for 4 h with CFA from Utah enriched in <1 micrometer particles (20 microgram/cm(2)) resulted in a 2.6-fold increase in mRNA levels for IL-8. 3-chloro-4-fluoroaniline 61-64 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. 3-chloro-4-fluoroaniline 139-142 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. 3-chloro-4-fluoroaniline 139-142 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. 3-chloro-4-fluoroaniline 203-206 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. 3-chloro-4-fluoroaniline 203-206 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. Metals 231-236 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. Metals 231-236 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. Deferoxamine 246-263 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. Deferoxamine 246-263 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. Metals 294-299 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. Metals 294-299 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. Iron 344-348 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10688536-6 2000 IL-8 levels were increased in the medium by as much as 8-fold when cells were treated with the fraction enriched in the smallest size Utah CFA for 24 h. IL-8 production was completely inhibited when the CFA was pretreated with the metal chelator desferrioxamine B, suggesting that a transition metal was responsible for the induction, probably iron. Iron 344-348 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 10688536-7 2000 Treatment with a soluble form of iron, ferric ammonium citrate (FAC), mimicked the IL-8 level increase observed with CFA. Iron 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 10688536-7 2000 Treatment with a soluble form of iron, ferric ammonium citrate (FAC), mimicked the IL-8 level increase observed with CFA. ferric ammonium citrate 39-62 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 10688536-8 2000 There was a direct relationship, above a threshold level of bioavailable iron, between the levels of IL-8 and bioavailable iron in A549 cells treated with CFA or FAC. Iron 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 10706503-2 2000 This study has tested the hypothesis that T-cell chemotaxis induced by platelet-activating factor (PAF) and human recombinant interleukin-8 (hrIL-8) can be attenuated by inhibition of phosphodiesterase activity and raised intracellular 3",5"-cyclic adenosine monophosphate (cAMP) levels. 3",5"-cyclic adenosine monophosphate 236-272 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 10688536-8 2000 There was a direct relationship, above a threshold level of bioavailable iron, between the levels of IL-8 and bioavailable iron in A549 cells treated with CFA or FAC. Iron 123-127 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 10706503-2 2000 This study has tested the hypothesis that T-cell chemotaxis induced by platelet-activating factor (PAF) and human recombinant interleukin-8 (hrIL-8) can be attenuated by inhibition of phosphodiesterase activity and raised intracellular 3",5"-cyclic adenosine monophosphate (cAMP) levels. Cyclic AMP 274-278 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 10688536-9 2000 Further, the relationship between IL-8 and bioavailable iron for CFA was indistinguishable from that for FAC. Iron 56-60 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 10688536-10 2000 These results strongly suggest that iron can induce IL-8 in A549 cells and that iron was the likely component of CFA that induced IL-8. Iron 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 10688536-10 2000 These results strongly suggest that iron can induce IL-8 in A549 cells and that iron was the likely component of CFA that induced IL-8. Iron 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 10688536-11 2000 CFA-induced IL-8 production was inhibited by tetramethylthiourea or dimethyl sulfoxide, suggesting that radical species were involved in the induction. 3-chloro-4-fluoroaniline 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 10688536-11 2000 CFA-induced IL-8 production was inhibited by tetramethylthiourea or dimethyl sulfoxide, suggesting that radical species were involved in the induction. tetramethylthiourea 45-64 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 10688536-11 2000 CFA-induced IL-8 production was inhibited by tetramethylthiourea or dimethyl sulfoxide, suggesting that radical species were involved in the induction. Dimethyl Sulfoxide 68-86 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 10685001-8 2000 Eighteen hour cytokine treatments with GM-CSF, IL-8, RANTES, IFN-gamma or TNF-alpha primed the cells for enhanced reactive oxygen species following exposure to an EOS stimulant. Reactive Oxygen Species 114-137 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 10615065-3 2000 In the present study we investigated the effects of clarithromycin (CAM) on interleukin (IL)-8 gene expression and protein levels, using the human bronchial epithelial cell line BET-1A. Clarithromycin 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 76-94 11450070-4 2000 The ischemia-induced expression of ICAM-1 in HCEC, and the expression/release of IL-8 and MCP-1 in HCEC were abolished by the non-steroid anti-inflammatory drug, indomethacin (100-300 microM). Indomethacin 162-174 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 11450070-5 2000 The immunosuppressant cyclosporin A (50 microM) partially reduced the ischemia-stimulated IL-8 and MCP-1 secretion by HCEC. Cyclosporine 22-35 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 10640773-3 2000 Exogenous hydrogen peroxide and neutrophils activated by IL-8, FMLP, or TNF-alpha increased EGFR tyrosine phosphorylation and subsequent activation of p44/42mapk and up-regulated the expression of MUC5AC at both mRNA and protein levels in NCI-H292 cells. Hydrogen Peroxide 10-27 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 10640773-3 2000 Exogenous hydrogen peroxide and neutrophils activated by IL-8, FMLP, or TNF-alpha increased EGFR tyrosine phosphorylation and subsequent activation of p44/42mapk and up-regulated the expression of MUC5AC at both mRNA and protein levels in NCI-H292 cells. Tyrosine 97-105 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 10620700-2 2000 Pretreatment of RSF with a specific p38 MAP kinase inhibitor, SB203580, blocked the induction of IL-6 and IL-8 without affecting nuclear translocation of nuclear factor kappaB (NF-kappaB) or IL-6 and IL-8 mRNA levels. (3r,3as,6ar)-Hexahydrofuro[2,3-B]furan-3-Ol 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 10620700-2 2000 Pretreatment of RSF with a specific p38 MAP kinase inhibitor, SB203580, blocked the induction of IL-6 and IL-8 without affecting nuclear translocation of nuclear factor kappaB (NF-kappaB) or IL-6 and IL-8 mRNA levels. (3r,3as,6ar)-Hexahydrofuro[2,3-B]furan-3-Ol 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 10620700-2 2000 Pretreatment of RSF with a specific p38 MAP kinase inhibitor, SB203580, blocked the induction of IL-6 and IL-8 without affecting nuclear translocation of nuclear factor kappaB (NF-kappaB) or IL-6 and IL-8 mRNA levels. SB 203580 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 10615065-0 2000 Interleukin-8 gene repression by clarithromycin is mediated by the activator protein-1 binding site in human bronchial epithelial cells. Clarithromycin 33-47 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 10615065-3 2000 In the present study we investigated the effects of clarithromycin (CAM) on interleukin (IL)-8 gene expression and protein levels, using the human bronchial epithelial cell line BET-1A. Clarithromycin 52-66 C-X-C motif chemokine ligand 8 Homo sapiens 76-94 10619832-6 2000 SB 203580, as the specific inhibitor of p38 MAP kinase activity, inhibited DEP-induced IL-8 and RANTES production. SB 203580 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 10619832-7 2000 NAC inhibited DEP-induced p38 MAP kinase activation and IL-8 and RANTES production. Acetylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 10615065-12 2000 These data suggest that macrolides such as CAM repress IL-8 gene transcription mainly via the AP-1 binding site in human bronchial epithelial cells. Macrolides 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 10615065-12 2000 These data suggest that macrolides such as CAM repress IL-8 gene transcription mainly via the AP-1 binding site in human bronchial epithelial cells. Clarithromycin 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 10853906-4 2000 The aim of the present study was to examine interleukin-8 (IL-8) in the synovial-like interface membrane (SLIM) and pseudocapsular tissue of THRs and to compare it to normal knee synovial membrane. Threonine 141-145 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 10853906-4 2000 The aim of the present study was to examine interleukin-8 (IL-8) in the synovial-like interface membrane (SLIM) and pseudocapsular tissue of THRs and to compare it to normal knee synovial membrane. Threonine 141-145 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 10853906-13 2000 The present study determines for the first time the cellular origin of IL-8 in aseptically loosened THRs and also quantitates the IL-8-producing cells in the periprosthetic tissue. Threonine 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 10867834-2 2000 We examined the in vivo and in vitro effects of 14-membered macrolide antibiotics erythromycin (EM) and clarithromycin (CAM) on interleukin (IL)-8 secretion from human nasal epithelial cells. Erythromycin 96-98 C-X-C motif chemokine ligand 8 Homo sapiens 128-146 10971057-0 2000 Adamantiades-Behcet"s disease: serum IL-8 is a more reliable marker for disease activity than C-reactive protein and erythrocyte sedimentation rate. adamantiades 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 10971057-1 2000 BACKGROUND: Interleukin 8 (IL-8) has recently been under focused investigation because of its possible participation in the evolution of Adamantiades-Behcet"s disease. adamantiades 137-149 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 10971057-1 2000 BACKGROUND: Interleukin 8 (IL-8) has recently been under focused investigation because of its possible participation in the evolution of Adamantiades-Behcet"s disease. adamantiades 137-149 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 10971057-8 2000 CONCLUSION: Our results confirm previous data concerning the significance of IL-8 and, in addition, they provide first evidence for the reliability of IL-8 as a serological marker for assessment of the activity of Adamantiades-Behcet"s disease in the follow-up of clinical and therapeutic studies. adamantiades 214-226 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 10623446-3 2000 The effect of modulating IL-8 activity upon the growth of the colon carcinoma cell lines HCT116A, HT29 and CaCo2 was investigated. caco2 107-112 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 10867834-0 2000 Effects of macrolides on interleukin-8 secretion from human nasal epithelial cells. Macrolides 11-21 C-X-C motif chemokine ligand 8 Homo sapiens 25-38 10867834-2 2000 We examined the in vivo and in vitro effects of 14-membered macrolide antibiotics erythromycin (EM) and clarithromycin (CAM) on interleukin (IL)-8 secretion from human nasal epithelial cells. Clarithromycin 104-118 C-X-C motif chemokine ligand 8 Homo sapiens 128-146 10867834-2 2000 We examined the in vivo and in vitro effects of 14-membered macrolide antibiotics erythromycin (EM) and clarithromycin (CAM) on interleukin (IL)-8 secretion from human nasal epithelial cells. Clarithromycin 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 128-146 10867834-2 2000 We examined the in vivo and in vitro effects of 14-membered macrolide antibiotics erythromycin (EM) and clarithromycin (CAM) on interleukin (IL)-8 secretion from human nasal epithelial cells. 14-membered macrolide antibiotics 48-81 C-X-C motif chemokine ligand 8 Homo sapiens 128-146 10867834-7 2000 When cells were preincubated with 10(-4) M CAM for 7 days, the IL-1 beta-induced secretion of IL-8 decreased significantly. Clarithromycin 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 10867834-2 2000 We examined the in vivo and in vitro effects of 14-membered macrolide antibiotics erythromycin (EM) and clarithromycin (CAM) on interleukin (IL)-8 secretion from human nasal epithelial cells. Erythromycin 82-94 C-X-C motif chemokine ligand 8 Homo sapiens 128-146 10867834-9 2000 These results suggest that macrolide treatment inhibits neutrophil infiltration and IL-8 secretion in nasal epithelium in vivo and that these clinical effects depend on a mechanism other than the direct action of macrolide on nasal epithelial cells. Macrolides 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 10671814-4 2000 However, the increases in PGE(2) production by IL-6 and IL-8 were found at relatively high concentrations, i.e. at 100 and 200 ng/ml. Prostaglandins E 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 12881895-8 2000 However, much more IL-8 was released into the tissue culture supernatant by SiO2 at the same levels of cytotoxicity than by Ni3S2. Silicon Dioxide 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 10603404-9 2000 In contrast to the response to LPS, where TNF-alpha, IL-1beta, IL-6, and IL-8 appear almost simultaneously, the human monocyte response to GBS results in the production of TNF-alpha but delayed appearance of IL-1beta, IL-6, and IL-8. gbs 139-142 C-X-C motif chemokine ligand 8 Homo sapiens 228-232 12881895-8 2000 However, much more IL-8 was released into the tissue culture supernatant by SiO2 at the same levels of cytotoxicity than by Ni3S2. ni3s2 124-129 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 10954057-4 2000 LPS also stimulated secretion of IL-6 and IL-8 in cultured trophoblasts, which was suppressed by nafamostat mesilate. nafamostat 97-116 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 11240649-0 2000 Cytokines IL-1beta, IL-2, IL-6, IL-8, MCP-1, GM-CSF and TNFalpha in patients with epithelial ovarian cancer and their relationship to treatment with paclitaxel. Paclitaxel 149-159 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 11240649-7 2000 In serum, IL-6, IL-8 and MCP-1 decreased with the administration of steroids prior to paclitaxel, and increased in the 24 h after paclitaxel. Steroids 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 11240649-10 2000 Treatment with paclitaxel is associated with an increase in expression of a limited number of cytokines in patients with ovarian cancer, notably IL-6, IL-8 and MCP-1. Paclitaxel 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 10970000-0 2000 Identification of a possible association between carbon tetrachloride-induced hepatotoxicity and interleukin-8 expression. Carbon Tetrachloride 49-69 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 10970000-8 2000 We also found that carbon tetrachloride caused a time-dependent increase in interleukin-8 protein release in HepG2 cells, which was paralleled by a decrease in cell viability. Carbon Tetrachloride 19-39 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 10970000-9 2000 These data demonstrate that carbon tetrachloride causes a rapid increase in IL-8 mRNA expression in HepG2 cells and that this increase correlates with a later and significant increase in the levels of interleukin-8 protein. Carbon Tetrachloride 28-48 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 10970000-9 2000 These data demonstrate that carbon tetrachloride causes a rapid increase in IL-8 mRNA expression in HepG2 cells and that this increase correlates with a later and significant increase in the levels of interleukin-8 protein. Carbon Tetrachloride 28-48 C-X-C motif chemokine ligand 8 Homo sapiens 201-214 10732314-2 2000 METHODS: Amnion-derived WISH cells were treated with a range of prostanoids and their effects on production of interleukin (IL)-6 and IL-8 were determined by enzyme-linked immunosorbent assay and Northern analysis. Prostaglandins 64-75 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 10670836-0 2000 Grepafloxacin inhibits tumor necrosis factor-alpha-induced interleukin-8 expression in human airway epithelial cells. grepafloxacin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 10670836-1 2000 We examined the effect of grepafloxacin (GPFX), a new fluoroquinolone antimicrobial agent, on interleukin-8 (IL-8) expression in tumor necrosis factor-alpha (TNF-alpha)-stimulated human airway epithelial cells (AEC). grepafloxacin 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 10670836-1 2000 We examined the effect of grepafloxacin (GPFX), a new fluoroquinolone antimicrobial agent, on interleukin-8 (IL-8) expression in tumor necrosis factor-alpha (TNF-alpha)-stimulated human airway epithelial cells (AEC). grepafloxacin 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10670836-1 2000 We examined the effect of grepafloxacin (GPFX), a new fluoroquinolone antimicrobial agent, on interleukin-8 (IL-8) expression in tumor necrosis factor-alpha (TNF-alpha)-stimulated human airway epithelial cells (AEC). grepafloxacin 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 94-107 10670836-1 2000 We examined the effect of grepafloxacin (GPFX), a new fluoroquinolone antimicrobial agent, on interleukin-8 (IL-8) expression in tumor necrosis factor-alpha (TNF-alpha)-stimulated human airway epithelial cells (AEC). grepafloxacin 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10670836-1 2000 We examined the effect of grepafloxacin (GPFX), a new fluoroquinolone antimicrobial agent, on interleukin-8 (IL-8) expression in tumor necrosis factor-alpha (TNF-alpha)-stimulated human airway epithelial cells (AEC). Fluoroquinolones 54-69 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10670836-3 2000 We discuss the modulatory effect of GPFX on IL-8 production in the context of its efficacy on controlling chronic airway inflammatory diseases. grepafloxacin 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 10941934-6 2000 Compared with that by viable bacterial cells, IL-8 secretion by stimulated epithelial cells and monocytes was reduced when the bacteria were heated and treated with glutaraldehyde. Glutaral 165-179 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 11188927-10 2000 For the dose-dependent differences of the effect of interleukin-8 we propose a two wheel model of an inositolphosphate-mediated, ATP-independent release of calcium from intracellular stores and a cyclic AMP-mediated, ATP-dependent uptake of calcium into the endoplasmatic reticulum. Inositol Phosphates 101-118 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 11188927-10 2000 For the dose-dependent differences of the effect of interleukin-8 we propose a two wheel model of an inositolphosphate-mediated, ATP-independent release of calcium from intracellular stores and a cyclic AMP-mediated, ATP-dependent uptake of calcium into the endoplasmatic reticulum. Adenosine Triphosphate 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 11188927-10 2000 For the dose-dependent differences of the effect of interleukin-8 we propose a two wheel model of an inositolphosphate-mediated, ATP-independent release of calcium from intracellular stores and a cyclic AMP-mediated, ATP-dependent uptake of calcium into the endoplasmatic reticulum. Calcium 156-163 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 11188927-10 2000 For the dose-dependent differences of the effect of interleukin-8 we propose a two wheel model of an inositolphosphate-mediated, ATP-independent release of calcium from intracellular stores and a cyclic AMP-mediated, ATP-dependent uptake of calcium into the endoplasmatic reticulum. Cyclic AMP 196-206 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 11188927-10 2000 For the dose-dependent differences of the effect of interleukin-8 we propose a two wheel model of an inositolphosphate-mediated, ATP-independent release of calcium from intracellular stores and a cyclic AMP-mediated, ATP-dependent uptake of calcium into the endoplasmatic reticulum. Adenosine Triphosphate 217-220 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 11188927-10 2000 For the dose-dependent differences of the effect of interleukin-8 we propose a two wheel model of an inositolphosphate-mediated, ATP-independent release of calcium from intracellular stores and a cyclic AMP-mediated, ATP-dependent uptake of calcium into the endoplasmatic reticulum. Calcium 241-248 C-X-C motif chemokine ligand 8 Homo sapiens 52-65 11132774-7 2000 However, only basal secretion of interleukin-8 in both undifferentiated and DMSO-differentiated U937 cells was significantly reduced by CsA at the highest concentration (200 ng/ mL). Dimethyl Sulfoxide 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 11132774-7 2000 However, only basal secretion of interleukin-8 in both undifferentiated and DMSO-differentiated U937 cells was significantly reduced by CsA at the highest concentration (200 ng/ mL). Cyclosporine 136-139 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 11132774-8 2000 At therapeutic concentrations in vivo, CsA exerts a predominant effect on IL-8 secretion by human mononuclear phagocytes. Cyclosporine 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 10616000-7 1999 Tau-Cl, but not Tau, inhibited cytokine-triggered synthesis of IL-6 (50% inhibitory concentration [IC50] approximately 225 microM) and IL-8 (IC50 approximately 450 microM) when added simultaneously with the stimuli. tau-cl 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 10683319-3 2000 Tetradecanoyl phorbol acetate (TPA) strongly increased the IL-8 and MCP-1 amounts in the culture supernatants of all five cell lines. Tetradecanoylphorbol Acetate 0-29 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 10683319-3 2000 Tetradecanoyl phorbol acetate (TPA) strongly increased the IL-8 and MCP-1 amounts in the culture supernatants of all five cell lines. Tetradecanoylphorbol Acetate 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 10867611-0 2000 Fluticasone propionate reduces serum interleukin-8 levels in asthmatic patients. Fluticasone 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 10619350-9 1999 RESULTS: There was a significant reduction in levels of TNF-alpha and IL-6 at a furosemide concentration of 0.5 x 10(-2) M and a reduction in IL-8 levels at 10(-2) M. This inhibition was comparable to that found with equivalent molar concentrations of hydrocortisone. Hydrocortisone 252-266 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 10559516-6 1999 However, IL-1beta-induced productions of both MCP-1 and IL-8 were dose-dependently suppressed by enrichment of cells with vitamin E. Vitamin E 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 10593333-10 1999 Production of IL-8, in response to LPS alone or in combination with PAF, was inhibited by SB202190, a specific p38 inhibitor. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 90-98 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 10594545-10 1999 CONCLUSIONS: These results suggest that cetirizine reduced the release of IL-8 from A549 cells stimulated with PMA and TNF-alpha, respectively, by lowering IL-8 gene expression. Cetirizine 40-50 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 10594545-0 1999 Cetirizine counter-regulates interleukin-8 release from human epithelial cells (A549) BACKGROUND: Cetirizine, a H1-receptor antagonist, exerts besides its well-known anti-allergic potential an array of anti-inflammatory activities. Cetirizine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 10594545-10 1999 CONCLUSIONS: These results suggest that cetirizine reduced the release of IL-8 from A549 cells stimulated with PMA and TNF-alpha, respectively, by lowering IL-8 gene expression. Cetirizine 40-50 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 10594545-0 1999 Cetirizine counter-regulates interleukin-8 release from human epithelial cells (A549) BACKGROUND: Cetirizine, a H1-receptor antagonist, exerts besides its well-known anti-allergic potential an array of anti-inflammatory activities. Cetirizine 98-108 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 10623427-12 1999 These results indicate that IL-8 synergizes and LIF potentiates the TNF-alpha PGE(2)effect which appears to be mediated mostly by increasing cPLA2 activity level. Prostaglandins E 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 10594545-2 1999 OBJECTIVE: We wondered whether cetirizine might influence the release of interleukin-8 (IL-8) from human epithelial cells activated with agonists distinct from histamine. Cetirizine 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 10594545-2 1999 OBJECTIVE: We wondered whether cetirizine might influence the release of interleukin-8 (IL-8) from human epithelial cells activated with agonists distinct from histamine. Cetirizine 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 10594545-6 1999 Pre-incubation with cetirizine diminished the IL-8 release from cells activated with TNF-alpha or PMA in a significant manner. Cetirizine 20-30 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 10594545-8 1999 Northern blot analysis revealed a reduced steady state level of IL-8 mRNA in cells pretreated with cetirizine and stimulated with TNF-alpha. Cetirizine 99-109 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 10588510-3 1999 We evaluated the interactions of IL-8 and GRO-alpha in priming human PMN calcium fluxes [Ca2+]i within circulatory environments. Calcium 73-80 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 10786156-5 1999 The amounts of fluoride recharged in RGIs increased with the concentration of NaF solution, but those of PMCRs exposed to all concentrations of NaF solutions were less than 1.5 ppm. Fluorides 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 10786156-5 1999 The amounts of fluoride recharged in RGIs increased with the concentration of NaF solution, but those of PMCRs exposed to all concentrations of NaF solutions were less than 1.5 ppm. Compomers 105-110 C-X-C motif chemokine ligand 8 Homo sapiens 144-147 10583451-1 1999 BACKGROUND: Capillary leakage of sodium-fluorescein (NaF) in the skin reflects capillary permeability and may be a marker of diabetes-associated microcirculatory abnormalities. Fluorescein 33-51 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 10583451-6 1999 Enalapril reduced NaF leakage (P < 0.05), mean arterial blood pressure (P < 0.05) and microalbuminuria (P < 0. Enalapril 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 10624772-6 1999 Furthermore, IL-8, Gro and MCP-1 concentrations decreased between 24 and 72 h. Immunocytochemistry indicated expression of IL-8 by pleural mesothelial cells 24 h, but not 72 h, following TCN administration. Tetracycline 187-190 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 10624772-6 1999 Furthermore, IL-8, Gro and MCP-1 concentrations decreased between 24 and 72 h. Immunocytochemistry indicated expression of IL-8 by pleural mesothelial cells 24 h, but not 72 h, following TCN administration. Tetracycline 187-190 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 10624772-7 1999 The data suggest that local elaboration of interleukin-8 and growth-related protein, in part of mesothelial origin, may influence neutrophil recruitment in tetracycline-induced pleuritis. Tetracycline 156-168 C-X-C motif chemokine ligand 8 Homo sapiens 43-56 10570304-0 1999 Lipoteichoic acid inhibits lipopolysaccharide-induced adhesion molecule expression and IL-8 release in human lung microvascular endothelial cells. lipoteichoic acid 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 10570304-2 1999 This study investigated the effects of lipoteichoic acid (LTA), a cell wall component of Gram-positive bacteria, alone and with LPS or TNF-alpha, on CAM expression and IL-8 release in human lung microvascular endothelial cells (HLMVEC). lipoteichoic acid 39-56 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 10570306-10 1999 Furthermore, MIP-2 and truncated GCP-2(9-78), but not intact GCP-2(1-92)/LIX, partially desensitized the calcium response to human IL-8 in human neutrophils. Calcium 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 10605950-13 1999 The next morning after exercise, the LPS-induced IL-8 production increased 137, 89, and 96%, respectively, in control, low-, and high-dose wine groups, probably due to a rise in epinephrine and activation of platelets. lps 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 10605950-13 1999 The next morning after exercise, the LPS-induced IL-8 production increased 137, 89, and 96%, respectively, in control, low-, and high-dose wine groups, probably due to a rise in epinephrine and activation of platelets. Epinephrine 178-189 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 10622468-0 1999 Interleukin-8 stimulates placental prostacyclin production in preeclampsia. Epoprostenol 35-47 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 10622468-1 1999 PROBLEM: Our purpose was to determine placental interleukin (IL)-8 production and its correlation with the prostacyclin production in normal and preeclamptic pregnancies and to evaluate the beneficial effect of IL-8 on prostacyclin production. Epoprostenol 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 48-66 10622468-1 1999 PROBLEM: Our purpose was to determine placental interleukin (IL)-8 production and its correlation with the prostacyclin production in normal and preeclamptic pregnancies and to evaluate the beneficial effect of IL-8 on prostacyclin production. Epoprostenol 219-231 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 10622468-2 1999 METHOD OF STUDY: We determined 1) the in vitro production of IL-8 and prostacyclin by placental villous tissues from normal and preeclamptic pregnancies and 2) the production of prostacyclin by villous tissues from preeclampsia treated with recombinant human IL-8 (rhIL-8). Epoprostenol 178-190 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 10622468-6 1999 3) Placental tissues treated with IL-8 exhibited a concentration-dependent increase in 6-keto PGF1alpha production. 6-Ketoprostaglandin F1 alpha 87-103 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 10622468-7 1999 CONCLUSIONS: Placental tissues from preeclampsia produce significantly less IL-8 than tissues from normal pregnancies, which correlates with decreased prostacyclin production. Epoprostenol 151-163 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 10622468-8 1999 IL-8 improves placental prostacyclin production in preeclampsia. Epoprostenol 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10614789-7 1999 Using a naturally occurring compound found in the colon of vertebrates, butyrate, we provide evidence in an intestinal cell line that alteration of IkappaB-beta expression can modulate the transcriptional activation of the interleukin-8 (IL-8) gene by preventing the nuclear translocation of NF-kappaB proteins. Butyrates 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 223-236 10614789-7 1999 Using a naturally occurring compound found in the colon of vertebrates, butyrate, we provide evidence in an intestinal cell line that alteration of IkappaB-beta expression can modulate the transcriptional activation of the interleukin-8 (IL-8) gene by preventing the nuclear translocation of NF-kappaB proteins. Butyrates 72-80 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 10620157-7 1999 The fluoride release for all of the materials increased after each exposure to NaF; however, the amount for the composite was very low. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 10587368-6 1999 Disruption of the actin cytoskeleton by treating ESC with cytochalasin D completely blocked the increase of IL-8 that was induced in response to integrin activation. Cytochalasin D 58-72 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 10657523-6 1999 BEAS-2B cells also responded to the botanical irritant, capsaicin (10 microM) with increases in [Ca(2+)](i) and IL-8 cytokine release after 4 h exposure. Capsaicin 56-65 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 10657523-7 1999 The IL-8 release was dependent on the presence of extracellular calcium. Calcium 64-71 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 10718111-1 1999 Increased production of prostaglandins and cytokines by amnion, particularly prostaglandin (PG) E2, interleukin (IL)-6 and IL-8, is thought to be an important event in infection-associated preterm labour. Prostaglandins 24-38 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 20654562-12 1999 BC, Triton X100 and DNCB upregulated IL-8 mRNA expression while only BC induced a significant increase in IL-1alpha mRNA expression. Octoxynol 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 20654562-12 1999 BC, Triton X100 and DNCB upregulated IL-8 mRNA expression while only BC induced a significant increase in IL-1alpha mRNA expression. Dinitrochlorobenzene 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 20654562-15 1999 Our data demonstrate that divergent IL-1alpha and IL-8 release profiles and corresponding mRNA upregulation characterize the response to the tested irritants and DNCB. Dinitrochlorobenzene 162-166 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 10553038-0 1999 Roles of intracellular calcium and NF-kappa B in the Clostridium difficile toxin A-induced up-regulation and secretion of IL-8 from human monocytes. Calcium 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 10553038-5 1999 Toxin A induced IL-8 expression at the level of gene transcription and this effect occurred through a mechanism requiring intracellular calcium and calmodulin activation. Calcium 136-143 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 10543746-9 1999 These findings indicate that EM is capable of inhibiting expression of the IL-8 gene in T cells through transcriptional inhibition and that this inhibition is mediated through a non-calcineurin-dependent signaling event in T lymphocytes. Erythromycin 29-31 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 10553845-8 1999 The increases in IL-8 and interferon gamma were 1.5-3 times greater during isoflurane than propofol anesthesia. Isoflurane 75-85 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 10553845-8 1999 The increases in IL-8 and interferon gamma were 1.5-3 times greater during isoflurane than propofol anesthesia. Propofol 91-99 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 10589757-0 1999 Discovery of differentially expressed genes associated with paclitaxel resistance using cDNA array technology: analysis of interleukin (IL) 6, IL-8, and monocyte chemotactic protein 1 in the paclitaxel-resistant phenotype. Paclitaxel 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 10589757-0 1999 Discovery of differentially expressed genes associated with paclitaxel resistance using cDNA array technology: analysis of interleukin (IL) 6, IL-8, and monocyte chemotactic protein 1 in the paclitaxel-resistant phenotype. Paclitaxel 191-201 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 10589791-5 1999 Immunohistochemical analysis of tumor lesions indicated that IL-8 overexpression was predominant in the regions surrounding necrotic areas, where cells were exposed to low oxygen tension (hypoxia) and acidic pH. Oxygen 172-178 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 10589791-9 1999 Decreased IL-8 expression after transfection with IL-8 antisense oligonucleotide expression vector retarded the growth of FG cells in mice after intrapancreatic implantation, which correlated with decreased tumor angiogenesis. Oligonucleotides 65-80 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 10589791-9 1999 Decreased IL-8 expression after transfection with IL-8 antisense oligonucleotide expression vector retarded the growth of FG cells in mice after intrapancreatic implantation, which correlated with decreased tumor angiogenesis. Oligonucleotides 65-80 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 10643587-6 1999 IL-8-induced inhibition was blocked partially by the protein kinase C (PKC) inhibitors, sphingosine, and H-7 1-(5-isoquinoline sulfonyl)-2-methylpiperazine. Sphingosine 88-99 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10596701-10 1999 BOS patients had significantly higher mean levels of MPO, ECP and IL-8 compared to patients without BOS, irrespective of acute rejection status. N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 10602388-0 1999 Fluoride-induced interleukin-6 and interleukin-8 synthesis in human epithelial lung cells. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 10602388-4 1999 Dose-response experiments showed a maximal release of IL-6 and IL-8 at a concentration of 5 mM NaF 24 h after addition. Sodium Fluoride 95-98 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 10602388-6 1999 Time-course experiments showed a NaF-induced IL-6 response at 5 h, whereas an IL-8 response was observed after 10 h. Cycloheximide treatment completely abolished the NaF-induced cytokine responses. Cycloheximide 117-130 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 10602388-6 1999 Time-course experiments showed a NaF-induced IL-6 response at 5 h, whereas an IL-8 response was observed after 10 h. Cycloheximide treatment completely abolished the NaF-induced cytokine responses. Sodium Fluoride 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 10602388-8 1999 The fluoride-induced effects on IL-6 and IL-8 release were strongly reduced by pretreatment with deferoxamine (an Al3+-chelator), and enhanced by addition of Al3+. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 10602388-8 1999 The fluoride-induced effects on IL-6 and IL-8 release were strongly reduced by pretreatment with deferoxamine (an Al3+-chelator), and enhanced by addition of Al3+. Deferoxamine 97-109 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 10602388-8 1999 The fluoride-induced effects on IL-6 and IL-8 release were strongly reduced by pretreatment with deferoxamine (an Al3+-chelator), and enhanced by addition of Al3+. ALUMINUM ION 114-118 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 10602388-8 1999 The fluoride-induced effects on IL-6 and IL-8 release were strongly reduced by pretreatment with deferoxamine (an Al3+-chelator), and enhanced by addition of Al3+. ALUMINUM ION 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 10602388-9 1999 This indicates that an AlF4-- complex, a known activator of GTP-binding proteins, is involved in fluoride-induced IL-6 and IL-8 responses in A549 cells. Guanosine Triphosphate 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 10602388-9 1999 This indicates that an AlF4-- complex, a known activator of GTP-binding proteins, is involved in fluoride-induced IL-6 and IL-8 responses in A549 cells. Fluorides 97-105 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 10571725-9 1999 Thalidomide did, however, induce a 2-4-fold increase in keratinocyte-derived interleukin-8, a pro-migratory cellular autocrine factor. Thalidomide 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 10568711-3 1999 PMN respond to both interleukin-8 and bacterial stimuli with calcium ([Ca2+]i) fluxes, which can initiate respiratory burst (RB). Calcium 61-68 C-X-C motif chemokine ligand 8 Homo sapiens 20-33 10576211-4 1999 The IL-8-guided migration through an imitation of inflammatory matrix, a fibrin gel, was impaired by 90% after treatment with 7 microM U0126, a specific inhibitor of the kinase of p44/42 kinase. U 0126 135-140 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 10583443-12 1999 Anti-PR-3 antibody induced endothelial IL-8 expression could be inhibited by cycloheximide. Cycloheximide 77-90 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 10531258-10 1999 Use of the specific p38/RK inhibitor SB202190 showed that blocking of this pathway results in decreased Stx-mediated IL-8 secretion. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 10592469-9 1999 IL-8 production was significantly inhibited by N-acetyl-L-cysteine, FK506 and MG-132, inhibitors of NF-kappaB activation and translocation. Acetylcysteine 47-66 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10592469-9 1999 IL-8 production was significantly inhibited by N-acetyl-L-cysteine, FK506 and MG-132, inhibitors of NF-kappaB activation and translocation. Tacrolimus 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10592469-9 1999 IL-8 production was significantly inhibited by N-acetyl-L-cysteine, FK506 and MG-132, inhibitors of NF-kappaB activation and translocation. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 78-84 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10528206-7 1999 In addition, decreased IL-8 priming of H2O2 production by PMN from RPP patients could account for a lower bactericidal capacity of PMN, leading to the large number of bacteria in the subgingival region of RPP patients. Hydrogen Peroxide 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 10602303-1 1999 This study examined the applicability of luminol-dependent chemiluminescence (CL) response of neutrophils to assess the degree of stress of spinal surgery by measuring the capacity of circulating neutrophils to produce reactive oxygen species and the levels of serum cytokines: interleukin(IL)-1beta, IL-6, IL-8, tumour necrosis factor (TNF)-alpha and granulocyte colony stimulating factor (G-CSF). Luminol 41-48 C-X-C motif chemokine ligand 8 Homo sapiens 307-311 10643587-6 1999 IL-8-induced inhibition was blocked partially by the protein kinase C (PKC) inhibitors, sphingosine, and H-7 1-(5-isoquinoline sulfonyl)-2-methylpiperazine. h-7 1-(5-isoquinoline sulfonyl)-2-methylpiperazine 105-155 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10643587-8 1999 CONCLUSION: IL-8 may increase the PAF concentration in the decidua via its inhibitory effect on PAF-AH secretion by decidual macrophages. Platelet Activating Factor 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 10521501-0 1999 Arsenite exposure of cultured airway epithelial cells activates kappaB-dependent interleukin-8 gene expression in the absence of nuclear factor-kappaB nuclear translocation. arsenite 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 10593592-0 1999 Sulfur mustard upregulates the expression of interleukin-8 in cultured human keratinocytes. Mustard Gas 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 10593592-5 1999 After 6 h, a significantly higher amount of IL-8 was secreted by human keratinocytes treated with 10(-4) M SM and the accumulation of the cytokine persisted up to 24 h after exposure. Mustard Gas 107-109 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 10598072-5 1999 In vitro chemotaxis of peripheral blood neutrophils to human C5a and ovine IL-8 was increased by dexamethasone treatment. Dexamethasone 97-110 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 10521501-3 1999 We compared intracellular signaling mediating IL-8 gene expression in bronchial epithelial cells cultured in vitro and exposed to two inducers of cellular stress, sodium arsenite (As(III)), and vanadyl sulfate (V(IV)). sodium arsenite 163-178 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 10521501-4 1999 Unstimulated bronchial epithelial cells expressed IL-8, and exposure to both metal compounds significantly enhanced IL-8 expression. Metals 77-82 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 10521501-5 1999 Overexpression of a dominant negative inhibitor of NF-kappaB depressed both basal and metal-induced IL-8 expression. Metals 86-91 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 10520061-9 1999 MPO and IL-8 were abundantly present in the sputum of all the TDI-induced asthmatic subjects and they increased significantly at 420 min after the bronchial challenges (P = 0.02, P = 0.03, respectively), while no significant changes were noted in group II subjects (P > 0.05). Toluene 2,4-Diisocyanate 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 10573218-9 1999 Procaterol inhibited the release of RANTES, GM-CSF and IL-8 in a dose-dependent fashion. Procaterol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 10614715-8 1999 MTX + EtOH increased the release of IL 6, IL 8 and TNF alpha by 1.0, 1.2, and 1.1 times, respectively. Methotrexate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 10614715-8 1999 MTX + EtOH increased the release of IL 6, IL 8 and TNF alpha by 1.0, 1.2, and 1.1 times, respectively. Ethanol 6-10 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 10540334-2 1999 Exposure of U937 cells to etoposide (VP-16) or the nitric oxide (NO) donor DETA-NO, both inducers of apoptosis in these cells, was associated with increased expression of the chemokines IL-8 and macrophage inflammatory protein-1 alpha. Etoposide 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 10540334-2 1999 Exposure of U937 cells to etoposide (VP-16) or the nitric oxide (NO) donor DETA-NO, both inducers of apoptosis in these cells, was associated with increased expression of the chemokines IL-8 and macrophage inflammatory protein-1 alpha. Nitric Oxide 51-63 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 10540334-2 1999 Exposure of U937 cells to etoposide (VP-16) or the nitric oxide (NO) donor DETA-NO, both inducers of apoptosis in these cells, was associated with increased expression of the chemokines IL-8 and macrophage inflammatory protein-1 alpha. DETA-NO 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 10540334-3 1999 Up-regulation of IL-8 mRNA expression by VP-16 or DETA-NO was observed as early as 4 h or 6 h, respectively, after onset of treatment and was still detectable after 19 h of exposure. DETA-NO 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 10540334-5 1999 Moreover, we observed that incubation with 2-chlorodeoxyadenosine (CdA) up-regulated release of IL-8 from adherent PBMC in parallel to induction of apoptosis. Cladribine 43-65 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 10540334-5 1999 Moreover, we observed that incubation with 2-chlorodeoxyadenosine (CdA) up-regulated release of IL-8 from adherent PBMC in parallel to induction of apoptosis. Cladribine 67-70 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 10540334-7 1999 In addition, CdA augmented release of IL-8 from whole blood cultures. Cladribine 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 10540155-6 1999 In the intestinal epithelial cell lines HT-29, T84 and Caco-2, sodium butyrate enhanced TNF-alpha-induced C3 secretion, but suppressed TNF-alpha-induced factor B and IL-8 secretion. Butyric Acid 63-78 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 10551153-10 1999 GM-CSF (50 IU/ml) also significantly increased IL-8 production from 2-7 days of treatment of THP-1 cells when supplemented with a positive control, phorbol-12-myristate-13 acetate (PMA), as compared to PMA treatment alone. Tetradecanoylphorbol Acetate 148-179 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 10537260-10 1999 The stimulation of IL-8 release was 4-fold (3-fold titanium particles) and of TNF-alpha. Titanium 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 10537260-13 1999 Rotation per se as well as exposure to increasing concentrations of PE and titanium particles stimulates cytokine release (TNF-alpha, IL-1beta, IL-8) by macrophages in vitro. Polyethylene 68-70 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 10537260-13 1999 Rotation per se as well as exposure to increasing concentrations of PE and titanium particles stimulates cytokine release (TNF-alpha, IL-1beta, IL-8) by macrophages in vitro. Titanium 75-83 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 10509360-0 1999 Mechanism for dexamethasone inhibition of neutrophil migration upon exposure to lipopolysaccharide in vitro: role of neutrophil interleukin-8 release. Dexamethasone 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 10504268-3 1999 Chemokines bind to glycosaminoglycans on human umbilical vein endothelial cells (HUVECs) with affinities in the micromolar range: RANTES > MCP-1 > IL-8 > MIP-1alpha. Glycosaminoglycans 19-37 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 10509360-9 1999 At 18 h, media-induced migration activity was decreased if DEX (10(-7) M), IL-8 antibody, or DEX (10(-7) M) with IL-8 antibody were present during the incubation with LPS: there was an 88, 86, and 101% reduction in migration activity, respectively. Dexamethasone 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 10509360-10 1999 We conclude that DEX inhibits PMN-induced PMN migration, predominantly via inhibition of IL-8 release for PMNs of the newborn. Dexamethasone 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 10948710-8 1999 Chemotaxis induced by fMLP and IL-8 was diminished when blood cells were incubated earlier with 50 mg of nadroparine. Nadroparin 105-116 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 10520180-3 1999 The chemotaxis of freshly isolated human granulocytes and differentiated HL-60 cells in response to the bacterial tripeptide, f-met-leu-phe, was inhibited in the presence of a physiological concentration of Hp, but chemotaxis in the presence of the proinflammatory cytokine interleukin-8 (IL-8) was not inhibited. tripeptide K-26 114-124 C-X-C motif chemokine ligand 8 Homo sapiens 274-287 10520180-3 1999 The chemotaxis of freshly isolated human granulocytes and differentiated HL-60 cells in response to the bacterial tripeptide, f-met-leu-phe, was inhibited in the presence of a physiological concentration of Hp, but chemotaxis in the presence of the proinflammatory cytokine interleukin-8 (IL-8) was not inhibited. tripeptide K-26 114-124 C-X-C motif chemokine ligand 8 Homo sapiens 289-293 10520180-3 1999 The chemotaxis of freshly isolated human granulocytes and differentiated HL-60 cells in response to the bacterial tripeptide, f-met-leu-phe, was inhibited in the presence of a physiological concentration of Hp, but chemotaxis in the presence of the proinflammatory cytokine interleukin-8 (IL-8) was not inhibited. N-Formylmethionine Leucyl-Phenylalanine 126-139 C-X-C motif chemokine ligand 8 Homo sapiens 274-287 10520180-3 1999 The chemotaxis of freshly isolated human granulocytes and differentiated HL-60 cells in response to the bacterial tripeptide, f-met-leu-phe, was inhibited in the presence of a physiological concentration of Hp, but chemotaxis in the presence of the proinflammatory cytokine interleukin-8 (IL-8) was not inhibited. N-Formylmethionine Leucyl-Phenylalanine 126-139 C-X-C motif chemokine ligand 8 Homo sapiens 289-293 10504268-8 1999 Isothermal titration calorimetry data confirm these results; IL-8 binds heparin fragments with a K(d) of 0.39-2.63 microM, and requires five saccharide units to bind each monomer of chemokine. Heparin 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 10504268-8 1999 Isothermal titration calorimetry data confirm these results; IL-8 binds heparin fragments with a K(d) of 0.39-2.63 microM, and requires five saccharide units to bind each monomer of chemokine. Carbohydrates 141-151 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 10504268-10 1999 Consistent with this, heparin and heparin sulfate could inhibit IL-8-induced neutrophil calcium flux. Heparin 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 10504268-10 1999 Consistent with this, heparin and heparin sulfate could inhibit IL-8-induced neutrophil calcium flux. Heparitin Sulfate 34-49 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 10504268-10 1999 Consistent with this, heparin and heparin sulfate could inhibit IL-8-induced neutrophil calcium flux. Calcium 88-95 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 10471323-4 1999 Incubation in vitro with jarastatin significantly inhibited, in a concentration-dependent manner, the chemotaxis of human neutrophils toward fMLP, IL-8, and jarastatin itself. jarastatin 25-35 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 10484459-3 1999 We now show that E1A-dependent induction of interleukin-8 expression is specific to LPS, superinduced by cycloheximide, and not observed after tumor necrosis factor or phorbol 12-myristate 13-acetate stimulation. Cycloheximide 105-118 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 10477716-3 1999 In this study, we investigate the role of TNFalpha-inducible reactive oxygen species (ROS) in IL-8 expression by "monocyte-like" U937 histiocytic lymphoma cells. Reactive Oxygen Species 61-84 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 10477716-3 1999 In this study, we investigate the role of TNFalpha-inducible reactive oxygen species (ROS) in IL-8 expression by "monocyte-like" U937 histiocytic lymphoma cells. Reactive Oxygen Species 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 17030330-1 1999 The nature of the contracted form of poly(methacrylic acid) PMA chain in salt-free acidic aqueous solution was studied by analyzing scattering curves registered by small-angle X-ray scattering, comparing it with those of PMA in methanol at 26 degrees C and of partially neutralized PMA in aqueous solution containing added salt (the concentration of added salt, Cs=0.1 M NaF). poly(methacrylic acid) pma 37-63 C-X-C motif chemokine ligand 8 Homo sapiens 371-374 11207549-1 1999 Using human endothelial cells, we define a mechanism that accounts for the induction of interleukin 8 (IL-8) by protein I/IIf, an adhesin from Streptococcus mutans serotype f. We report that protein I/IIf interactions with endothelial cells increased the tyrosine phosphorylation of three cellular components with relative mass of 145,000, 125,000 and 70,000 in endothelial cells. Tyrosine 255-263 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 10475301-9 1999 In this study, we demonstrated that ketamine directly inhibits the production of proinflammatory cytokines such as TNF-alpha, IL-6, and IL-8 in human whole blood. Ketamine 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 10475301-10 1999 IMPLICATIONS: We found that ketamine suppressed lipopolysaccharide-induced tumor necrosis factor alpha, interleukin (IL)-6, and IL-8 production and recombinant human tumor necrosis factor-induced IL-6 and IL-8 production in human whole blood. Ketamine 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 10475301-10 1999 IMPLICATIONS: We found that ketamine suppressed lipopolysaccharide-induced tumor necrosis factor alpha, interleukin (IL)-6, and IL-8 production and recombinant human tumor necrosis factor-induced IL-6 and IL-8 production in human whole blood. Ketamine 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 10625945-4 1999 An increase in IL-8 secretion by stimulated cells occurred in the presence of IP6. Phytic Acid 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 10513809-11 1999 SP inhibited cytokine-stimulated HMVEC expression of IL-8 and MCP-1 (P<0.05; [n = 4]). Sulfapyridine 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 10513809-13 1999 CONCLUSION: These results demonstrate that SSZ and its metabolite SP may affect the pathogenesis of RA by inhibiting EC chemotaxis, proliferation, tube formation, and expression of sICAM-1, IL-8, and MCP-1. Sulfasalazine 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 10513809-13 1999 CONCLUSION: These results demonstrate that SSZ and its metabolite SP may affect the pathogenesis of RA by inhibiting EC chemotaxis, proliferation, tube formation, and expression of sICAM-1, IL-8, and MCP-1. Sulfapyridine 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 10475301-8 1999 At concentrations >100 microg/mL, ketamine also significantly suppressed both LPS-induced and rhTNF-induced IL-6 and IL-8 production. Ketamine 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 11207549-1 1999 Using human endothelial cells, we define a mechanism that accounts for the induction of interleukin 8 (IL-8) by protein I/IIf, an adhesin from Streptococcus mutans serotype f. We report that protein I/IIf interactions with endothelial cells increased the tyrosine phosphorylation of three cellular components with relative mass of 145,000, 125,000 and 70,000 in endothelial cells. Tyrosine 255-263 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 10425270-5 1999 In contrast, the pro-inflammatory cytokine TNFalpha, whose activity is dependent on the generation of intracellular ROS, induces IL-8 and ICAM-1 in both cell types. Reactive Oxygen Species 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 10464065-9 1999 The short-chain fatty acids, acetate, propionate, butyrate and valerate, the activator of protein kinase C (phorbol-12-myristate-13-acetate) and tumour necrosis factor-alpha (TNF-alpha) all stimulated the secretion of IL-8. Tetradecanoylphorbol Acetate 108-139 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 10487957-10 1999 IL-8 RNA level correlated with corneal fluorescein staining (rho 0.690, P = 0.001) and conjunctival goblet cell density (rho -0.767, P < 0.001). Fluorescein 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10425270-6 1999 The differential induction of IL-8 and ICAM-1 by H2O2 and TNFalpha suggest that the two inflammatory stimuli target distinct redox responsive signaling pathways to activate cell type-specific gene expression. Hydrogen Peroxide 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 10425270-1 1999 Reactive oxygen species (ROS), generated either extracellularly or intracellularly through ligand-receptor interactions, can function as signal transduction molecules to activate the chemotactic cytokine interleukin-8 (IL-8) and the cell surface adhesion protein, intercellular adhesion molecule-1 (ICAM-1; CD54). Reactive Oxygen Species 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 204-217 10425270-1 1999 Reactive oxygen species (ROS), generated either extracellularly or intracellularly through ligand-receptor interactions, can function as signal transduction molecules to activate the chemotactic cytokine interleukin-8 (IL-8) and the cell surface adhesion protein, intercellular adhesion molecule-1 (ICAM-1; CD54). Reactive Oxygen Species 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 10483900-10 1999 In the in vitro experiment, sodium butyrate dose-dependently inhibited tumor necrosis factor (TNF)-alpha-induced IL-8 secretion in HT-29 cells. Butyric Acid 28-43 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 10425270-1 1999 Reactive oxygen species (ROS), generated either extracellularly or intracellularly through ligand-receptor interactions, can function as signal transduction molecules to activate the chemotactic cytokine interleukin-8 (IL-8) and the cell surface adhesion protein, intercellular adhesion molecule-1 (ICAM-1; CD54). Reactive Oxygen Species 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 204-217 10425270-1 1999 Reactive oxygen species (ROS), generated either extracellularly or intracellularly through ligand-receptor interactions, can function as signal transduction molecules to activate the chemotactic cytokine interleukin-8 (IL-8) and the cell surface adhesion protein, intercellular adhesion molecule-1 (ICAM-1; CD54). Reactive Oxygen Species 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 219-223 10425270-3 1999 Recent results demonstrate that oxidant stress generated directly by exogenous H2O2 differentially induce IL-8 and ICAM-1 transcription in epithelial and endothelial cells. Hydrogen Peroxide 79-83 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 10425270-4 1999 H2O2 induces IL-8 but not ICAM-1 in the A549 type-II-like epithelial cell line, whereas in a microvessel endothelial cell line (HMEC-1) as well as in primary endothelial cells, H2O2 induces ICAM-1 but not IL-8, which is spontaneously expressed. Hydrogen Peroxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 10425270-4 1999 H2O2 induces IL-8 but not ICAM-1 in the A549 type-II-like epithelial cell line, whereas in a microvessel endothelial cell line (HMEC-1) as well as in primary endothelial cells, H2O2 induces ICAM-1 but not IL-8, which is spontaneously expressed. Hydrogen Peroxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 10469049-8 1999 In contrast, LPMC released IL-8 (650 +/- 125 pg/ml) and IL-10 (75 +/- 25 pg/ml) in response to LPS. lpmc 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 10469768-8 1999 RESULTS: At the first suspicion of NBI, the combination of IL-8 >/= 53 pg/mL and/or CRP >10 mg/L detected culture-proven NBI with 96% sensitivity. 2-Nitro-N-Phenylbenzamide 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 10551904-3 1999 We hypothesized that butyrate may alter IL-8 and MCP-1 expression by intestinal epithelial cells through histone acetylation. Butyrates 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 10551904-9 1999 In contrast, butyrate increased IL-8 production. Butyrates 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 10497395-4 1999 Reactive oxygen intermediates induce some cytokine gene expression such as IL-8. reactive oxygen 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 10438951-5 1999 The present study shows that the synthetic glucocorticoid, dexamethasone, inhibits the induction of the proinflammatory cytokine IL-8 and the adhesion molecules VCAM-1 and ICAM-1 in human 1321N1 astrocytoma and SK.N.SH neuroblastoma cells. Dexamethasone 59-72 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 10438717-4 1999 IL-8 mRNA expression is blocked by the protein kinase C inhibitor bisindolylmaleimide or protein tyrosine kinase inhibitors, genestein and geldanamycin, establishing the involvement of the protein kinase C and protein tyrosine kinase pathways in the activation process. bisindolylmaleimide 66-85 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10438717-4 1999 IL-8 mRNA expression is blocked by the protein kinase C inhibitor bisindolylmaleimide or protein tyrosine kinase inhibitors, genestein and geldanamycin, establishing the involvement of the protein kinase C and protein tyrosine kinase pathways in the activation process. geldanamycin 139-151 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10423406-4 1999 MBP stimulated 2-fold increases in IL-8 messenger RNA (mRNA) after 1 and 3 h of incubation, which were blocked by pretreatment with actinomycin D. Dactinomycin 132-145 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 10423413-10 1999 Although HBECs required stimulation by both CSE and C5a to release maximal levels of IL-8, preincubation of CSE-stimulated HBECs with calphostin C inhibited IL-8 release by CSE + C5a. calphostin C 134-146 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 10433940-0 1999 Genistein inhibits constitutive and inducible NFkappaB activation and decreases IL-8 production by human cystic fibrosis bronchial gland cells. Genistein 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 10433940-4 1999 We also demonstrated that the isoflavone genistein, a well known CFTR mutant Cl(-) channel stimulator, significantly reduces the endogenous and Pseudomonas aeruginosa lipopolysaccharide-induced IL-8 production in cultured CF bronchial gland cells by increasing cytosolic IkappaBalpha protein levels. Isoflavones 30-40 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 10423413-10 1999 Although HBECs required stimulation by both CSE and C5a to release maximal levels of IL-8, preincubation of CSE-stimulated HBECs with calphostin C inhibited IL-8 release by CSE + C5a. calphostin C 134-146 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 10433940-4 1999 We also demonstrated that the isoflavone genistein, a well known CFTR mutant Cl(-) channel stimulator, significantly reduces the endogenous and Pseudomonas aeruginosa lipopolysaccharide-induced IL-8 production in cultured CF bronchial gland cells by increasing cytosolic IkappaBalpha protein levels. Genistein 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 10433808-3 1999 We have investigated the effects of 5 lipid mediators (PAF, PGE(2), LTB(4), 12-HETE and 15-HETE) on the spontaneous and cytokine-induced IL-8 synthesis by human bone marrow stromal cells. Platelet Activating Factor 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 10433940-6 1999 This strong inhibition of constitutively activated NFkappaB and the resulting down-regulation of IL-8 production by genistein in the CF gland cells highlights the key role played by cytosolic IkappaBalpha in the regulation of inflammatory processes in CF human airway cells. Genistein 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10433808-3 1999 We have investigated the effects of 5 lipid mediators (PAF, PGE(2), LTB(4), 12-HETE and 15-HETE) on the spontaneous and cytokine-induced IL-8 synthesis by human bone marrow stromal cells. Prostaglandins E 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 10433808-3 1999 We have investigated the effects of 5 lipid mediators (PAF, PGE(2), LTB(4), 12-HETE and 15-HETE) on the spontaneous and cytokine-induced IL-8 synthesis by human bone marrow stromal cells. Leukotriene B4 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 10433808-5 1999 By using a specific ELISA, we found that the production of IL-8 by marrow stromal cells is enhanced after stimulation with 12-HETE (1 microM) both in serum-free and serum-containing culture medium. 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid 123-130 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 10433808-8 1999 PGE(2)(1 microM or 10 nM) reduces marrow stromal cell IL-8 synthesis in response to IL-1alpha or TNF-alpha. Dinoprostone 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 10417153-5 1999 Further studies with the L5F11 cell line showed that IL-8 gene transcription induced by H. pylori was blocked by the protein tyrosine kinase inhibitor herbimycin A but not by the protein kinase C inhibitor calphostin C or by the protein kinase G inhibitor KT5823. herbimycin 151-163 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 10485423-16 1999 However, significantly lower interleukin 8 release and complement activation can be achieved by heparin coating. Heparin 96-103 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 10457157-7 1999 Co-incubation of MSG with mannan or beta-glucan decreased IL-8 release by 48% and 42% respectively, suggesting that MSG stimulates A549 cells in part through carbohydrate moieties. Mannans 26-32 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 10457157-7 1999 Co-incubation of MSG with mannan or beta-glucan decreased IL-8 release by 48% and 42% respectively, suggesting that MSG stimulates A549 cells in part through carbohydrate moieties. beta-Glucans 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 10457157-8 1999 Dexamethasone significantly inhibited MSG-induced IL-8 release in concentrations of 10-6-10-8 mol L-1 compared with control experiments (P < 0.01). Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 10417153-5 1999 Further studies with the L5F11 cell line showed that IL-8 gene transcription induced by H. pylori was blocked by the protein tyrosine kinase inhibitor herbimycin A but not by the protein kinase C inhibitor calphostin C or by the protein kinase G inhibitor KT5823. KT 5823 256-262 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 10417209-3 1999 Lipoarabinomannan induced IL-8, MCP-1, and MIP-1beta in vitro, which was partly inhibited by anti-tumor necrosis factor antibody. lipoarabinomannan 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 10457212-5 1999 There were highly significant intercorrelations among milk Na/K ratio and concentrations of IL-8 and TGF-beta, the last only after treatment with bile salts which also improved TGF-beta recovery in the enzyme-linked immunosorbent assay (ELISA). Bile Acids and Salts 146-156 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 10457212-7 1999 Dietary supplementation with vitamin E-rich sunflower oil but not provitamin A-containing red palm oil decreased milk Na/K, IL-8 and TGF-beta at 3 months postpartum; however, the effect was significant only for Na/K ratio. Vitamin E 29-38 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 10453373-0 1999 Transdermal nicotine decreases mucosal IL-8 expression but has no effect on mucin gene expression in ulcerative colitis. Nicotine 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 10634174-7 1999 IL-8 induced a rapid increase of PBG (7-12-fold the basal values). pbg 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10453373-9 1999 IL-8 mRNA levels were significantly decreased in the colonic mucosa of nicotine-treated patients who improved (p = 0.04). Nicotine 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10453373-10 1999 IL-8 mRNA values were similar before and after treatment in nonresponding nicotine-treated patients and in all placebo-treated patients. Nicotine 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10453373-12 1999 Beneficial effects of transdermal nicotine in active UC may result from decrease of IL-8 expression at the transcriptional level. Nicotine 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 10462040-3 1999 IL-8 induction by TNF-alpha was redox sensitive, as indicated by electron spin resonance analysis and inhibition with membrane permeable hydroxyl scavengers. Hydroxyl Radical 137-145 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10565558-6 1999 After budesonide treatment, the correlation between IL-8 and neutrophils remained, and a correlation between IL-8 and eosinophils emerged. Budesonide 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 10565558-6 1999 After budesonide treatment, the correlation between IL-8 and neutrophils remained, and a correlation between IL-8 and eosinophils emerged. Budesonide 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 10565558-9 1999 It is possible that neutrophils, through the release of IL-8, could be chemotactic for eosinophils in steroid-treated patients. Steroids 102-109 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 10442524-7 1999 The steroids only partially inhibited IL-8 release from alveolar macrophages. Steroids 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 10383461-7 1999 Importantly, the genes for TNF-alpha, IL-8, and MHC class II, but not ICAM-1 or MHC class I, contain cyclic AMP response element (CRE) consensus motifs. Cyclic AMP 101-111 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 10455891-5 1999 RESULTS: Priming by tumor necrosis factor alpha (TNF-alpha), interleukin-8 (IL-8), and granulocyte-macrophage colony-stimulating factor (GM-CSF) was significantly inhibited by SB203580, whereas platelet-activating factor (PAF) priming was unaffected. SB 203580 176-184 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 11671064-5 1999 Extended refluxing of TpRe(O)I(2) with an excess of NaF in acetonitrile in the air gives a modest yield of an unusual rhenium &mgr;-pyrazolyl &mgr;-oxo dimer, {[kappa(2)-H(F)Bpz(2)]Re(O)}(2)(&mgr;-pz)(2)(&mgr;-O) (5) (pz = pyrazolyl). acetonitrile 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 11671064-5 1999 Extended refluxing of TpRe(O)I(2) with an excess of NaF in acetonitrile in the air gives a modest yield of an unusual rhenium &mgr;-pyrazolyl &mgr;-oxo dimer, {[kappa(2)-H(F)Bpz(2)]Re(O)}(2)(&mgr;-pz)(2)(&mgr;-O) (5) (pz = pyrazolyl). Adenosine Monophosphate 127-130 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 11671064-5 1999 Extended refluxing of TpRe(O)I(2) with an excess of NaF in acetonitrile in the air gives a modest yield of an unusual rhenium &mgr;-pyrazolyl &mgr;-oxo dimer, {[kappa(2)-H(F)Bpz(2)]Re(O)}(2)(&mgr;-pz)(2)(&mgr;-O) (5) (pz = pyrazolyl). pyrazolyl 136-145 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 11671064-5 1999 Extended refluxing of TpRe(O)I(2) with an excess of NaF in acetonitrile in the air gives a modest yield of an unusual rhenium &mgr;-pyrazolyl &mgr;-oxo dimer, {[kappa(2)-H(F)Bpz(2)]Re(O)}(2)(&mgr;-pz)(2)(&mgr;-O) (5) (pz = pyrazolyl). Adenosine Monophosphate 147-150 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 11671064-5 1999 Extended refluxing of TpRe(O)I(2) with an excess of NaF in acetonitrile in the air gives a modest yield of an unusual rhenium &mgr;-pyrazolyl &mgr;-oxo dimer, {[kappa(2)-H(F)Bpz(2)]Re(O)}(2)(&mgr;-pz)(2)(&mgr;-O) (5) (pz = pyrazolyl). bpz 182-185 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 11671064-5 1999 Extended refluxing of TpRe(O)I(2) with an excess of NaF in acetonitrile in the air gives a modest yield of an unusual rhenium &mgr;-pyrazolyl &mgr;-oxo dimer, {[kappa(2)-H(F)Bpz(2)]Re(O)}(2)(&mgr;-pz)(2)(&mgr;-O) (5) (pz = pyrazolyl). Adenosine Monophosphate 147-150 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 11671064-5 1999 Extended refluxing of TpRe(O)I(2) with an excess of NaF in acetonitrile in the air gives a modest yield of an unusual rhenium &mgr;-pyrazolyl &mgr;-oxo dimer, {[kappa(2)-H(F)Bpz(2)]Re(O)}(2)(&mgr;-pz)(2)(&mgr;-O) (5) (pz = pyrazolyl). Adenosine Monophosphate 147-150 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 11671064-5 1999 Extended refluxing of TpRe(O)I(2) with an excess of NaF in acetonitrile in the air gives a modest yield of an unusual rhenium &mgr;-pyrazolyl &mgr;-oxo dimer, {[kappa(2)-H(F)Bpz(2)]Re(O)}(2)(&mgr;-pz)(2)(&mgr;-O) (5) (pz = pyrazolyl). pyrazolyl 239-248 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 10442524-10 1999 In conclusion, budesonide and fluticasone propionate, in concentrations that probably occur in the airway lining fluid during inhalational therapy, inhibited cytokine release from human lung epithelial cells (IL-6, IL-8) and alveolar macrophages (TNF-alpha, IL-6, IL-8). Budesonide 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 10442524-10 1999 In conclusion, budesonide and fluticasone propionate, in concentrations that probably occur in the airway lining fluid during inhalational therapy, inhibited cytokine release from human lung epithelial cells (IL-6, IL-8) and alveolar macrophages (TNF-alpha, IL-6, IL-8). Budesonide 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 10442524-10 1999 In conclusion, budesonide and fluticasone propionate, in concentrations that probably occur in the airway lining fluid during inhalational therapy, inhibited cytokine release from human lung epithelial cells (IL-6, IL-8) and alveolar macrophages (TNF-alpha, IL-6, IL-8). Fluticasone 30-52 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 10442524-10 1999 In conclusion, budesonide and fluticasone propionate, in concentrations that probably occur in the airway lining fluid during inhalational therapy, inhibited cytokine release from human lung epithelial cells (IL-6, IL-8) and alveolar macrophages (TNF-alpha, IL-6, IL-8). Fluticasone 30-52 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 10414449-5 1999 Our results have shown that ATRA induces an increased expression of IL-8, IL-1beta, TNF-alpha and ICAM-1 in APL cells, which can be amplified by the addition of G-CSF. Tretinoin 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10391852-6 1999 In addition, proinflammatory cytokine (interleukin 1beta [IL-1beta] and tumor necrosis factor alpha [TNF-alpha]) levels are greater in culture wells containing discs of polyolefin polymer than in those containing discs of polyvinyl chloride polymer with the TEHTM plasticizer, and even more so in storage bags containing polyolefin polymer versus polyvinyl chloride polymer with the TEHTM plasticizer (IL-1beta, TNF-alpha, IL-6, and IL-8). polyolefin polymer 169-187 C-X-C motif chemokine ligand 8 Homo sapiens 433-437 10456399-10 1999 The TCA group had significantly higher levels of IL-6 (P = 0.001), IL-8 (P = 0.005) and S100B (P = 0.002) at 24 h. C5b-9 levels were significantly lower in the TCA group: end of CPB (P = 0.001), 30 min (P < 0.001), 2 h (P = 0.002). Trichloroacetic Acid 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 10489835-0 1999 Thiol regulation of the production of TNF-alpha, IL-6 and IL-8 by human alveolar macrophages. Sulfhydryl Compounds 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 10456399-13 1999 CONCLUSIONS: (1) The TCA group have prolonged rises of IL-6, IL-8 and S100B. Trichloroacetic Acid 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 10489835-4 1999 Depletion of intracellular GSH by treatment with buthionine sulphoximine (BSO) reached 45.2% after 3 h and was nearly complete at 24 h. Whereas a 24-h preincubation of AMs with BSO significantly increased LPS-induced secretion of TNF-alpha and IL-8, a 3-h preincubation only enhanced LPS-stimulated production of IL-8 (p<0.05). Glutathione 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 10353855-5 1999 Compared with placebo, rimantadine treatment reduced viral shedding, systemic symptoms, and levels of IL-8. Rimantadine 23-34 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 10489835-4 1999 Depletion of intracellular GSH by treatment with buthionine sulphoximine (BSO) reached 45.2% after 3 h and was nearly complete at 24 h. Whereas a 24-h preincubation of AMs with BSO significantly increased LPS-induced secretion of TNF-alpha and IL-8, a 3-h preincubation only enhanced LPS-stimulated production of IL-8 (p<0.05). Glutathione 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 313-317 10489835-4 1999 Depletion of intracellular GSH by treatment with buthionine sulphoximine (BSO) reached 45.2% after 3 h and was nearly complete at 24 h. Whereas a 24-h preincubation of AMs with BSO significantly increased LPS-induced secretion of TNF-alpha and IL-8, a 3-h preincubation only enhanced LPS-stimulated production of IL-8 (p<0.05). Buthionine Sulfoximine 49-72 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 10489835-4 1999 Depletion of intracellular GSH by treatment with buthionine sulphoximine (BSO) reached 45.2% after 3 h and was nearly complete at 24 h. Whereas a 24-h preincubation of AMs with BSO significantly increased LPS-induced secretion of TNF-alpha and IL-8, a 3-h preincubation only enhanced LPS-stimulated production of IL-8 (p<0.05). Buthionine Sulfoximine 49-72 C-X-C motif chemokine ligand 8 Homo sapiens 313-317 10489835-4 1999 Depletion of intracellular GSH by treatment with buthionine sulphoximine (BSO) reached 45.2% after 3 h and was nearly complete at 24 h. Whereas a 24-h preincubation of AMs with BSO significantly increased LPS-induced secretion of TNF-alpha and IL-8, a 3-h preincubation only enhanced LPS-stimulated production of IL-8 (p<0.05). Buthionine Sulfoximine 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 10489835-4 1999 Depletion of intracellular GSH by treatment with buthionine sulphoximine (BSO) reached 45.2% after 3 h and was nearly complete at 24 h. Whereas a 24-h preincubation of AMs with BSO significantly increased LPS-induced secretion of TNF-alpha and IL-8, a 3-h preincubation only enhanced LPS-stimulated production of IL-8 (p<0.05). Buthionine Sulfoximine 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 313-317 10489835-6 1999 Addition of GSH and NAC significantly reduced the secretion of TNF-alpha (mean+/-SEM 21.2+/-5 and 44.7+/-4.4% inhibition, respectively) as well as LPS-induced IL-6 and IL-8 (p<0.05). Glutathione 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 10489835-6 1999 Addition of GSH and NAC significantly reduced the secretion of TNF-alpha (mean+/-SEM 21.2+/-5 and 44.7+/-4.4% inhibition, respectively) as well as LPS-induced IL-6 and IL-8 (p<0.05). Acetylcysteine 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 10489835-7 1999 Similarly, NAC inhibited the production of TNF-alpha, IL-6 and IL-8 in GSH-depleted AMs obtained by BSO pretreatment. Acetylcysteine 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 10489835-7 1999 Similarly, NAC inhibited the production of TNF-alpha, IL-6 and IL-8 in GSH-depleted AMs obtained by BSO pretreatment. Glutathione 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 10489835-8 1999 In conclusion, N-acetylcysteine and glutathione inhibit the production of tumour necrosis factor-alpha, interleukin-8 and interleukin-6 by alveolar macrophages by a mechanism independent of glutathione metabolism. Acetylcysteine 15-31 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 10489835-8 1999 In conclusion, N-acetylcysteine and glutathione inhibit the production of tumour necrosis factor-alpha, interleukin-8 and interleukin-6 by alveolar macrophages by a mechanism independent of glutathione metabolism. Glutathione 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 10489835-9 1999 However, total depletion of glutathione within alveolar macrophages significantly increases tumour necrosis factor-alpha and interleukin-8 synthesis whereas it does not modulate interleukin-6 secretion. Glutathione 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 125-138 10400845-6 1999 NO2 also significantly increased the release of IL-8 from a control value of 52.5 pg/microgram cellular protein to 81.9 pg/microgram cellular protein (P <.05), RANTES from a control value of 0.023 pg/microgram cellular protein to 0.062 pg/microgram cellular protein (P <.05), and sICAM-1 from a control value of 7.7 pg/microgram cellular protein to 16.3 pg/microgram cellular protein (P <.05). Nitrogen Dioxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 10404837-6 1999 Midluteal endometrium showed minimal IL-8 expression, whereas endometrium obtained from women administered progesterone for 4 days from (LH peak + 8 days), to simulate luteal regression, demonstrated significantly increased localization of IL-8 mRNA, 48 h after withdrawal of progesterone. Progesterone 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 240-244 10412778-0 1999 Rapid normalization of interleukin-8 production after low-density lipoprotein apheresis in steroid-resistant nephrotic syndrome. Steroids 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 10398759-7 1999 Preincubation of SR with NaF and ATP, but not with NaF and AMP-PNP caused strong inhibition of ryanodine binding. Ryanodine 95-104 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 10412778-8 1999 IL-8 production by lipopolysaccharide (LPS)-stimulated PBMC, mainly adherent cells, was significantly reduced in both the steroid-resistant FGS group and nontreated NS group compared with controls, but TNF-alpha production was reduced in the only FGS group. Steroids 122-129 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10412778-10 1999 CONCLUSION: Significant amelioration of IL-8 production independent of any effect of steroids on LPS-stimulated PBMCs may reflect a beneficial effect of LDL-A in normalizing the function of circulating monocytes in steroid-resistant FGS. ldl-a 153-158 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 10463330-4 1999 IL-8, which activates a CXC receptor coupled to PTX-sensitive G proteins, induced at 10 nM an enhanced maximum chemotaxis of neutrophils from individuals with TC/TT genotype compared to CC genotype. Technetium 159-161 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10381841-6 1999 In this study, we set out to investigate a potential linkage between the generation of ROS and production of IL8 in alpha-particle-irradiated normal human lung fibroblasts. Reactive Oxygen Species 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 16801094-1 1999 We found that nafamostat mesilate (NM) inhibits platelet aggregation induced by all agonists tested, including ADP, collagen, arachidonic acid, thromboxane A analog, A23187, phorbol 12-myristate 13-acetate (PMA), NaF and thrombin. nafamostat 14-33 C-X-C motif chemokine ligand 8 Homo sapiens 213-216 10381841-9 1999 Cells exposed to alpha particles in the presence of antioxidants, i.e. superoxide dismutase and dimethyl sulfoxide, resulted in significant decreases in extracellular IL8 protein levels. Dimethyl Sulfoxide 96-114 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 10381841-11 1999 Our results indicate that alpha-particle-induced increases in production of IL8 occur temporally in parallel with elevated production of ROS. Reactive Oxygen Species 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 10358198-8 1999 LPS-induced IL-8 and TNF-alpha production was inhibited in a similar pattern by pretreatment with either EtOH or SB202190 (1 microM), a specific inhibitor of p38 kinase. 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole 113-121 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 10418175-7 1999 Serum IL-8 levels decreased gradually with abstinence from alcohol. Alcohols 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 10353264-0 1999 Up-regulation of interleukin-1beta-stimulated interleukin-8 in human keratinocytes by nitric oxide. Nitric Oxide 86-98 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 10353264-3 1999 Incubation with the NO donor S-nitroso-N-acetylpenicillamine (SNAP) for 24 hr increased IL-8 protein only in HaCaT cells, partly due to the presence of constitutive interleukin-1 (IL-1). S-Nitroso-N-Acetylpenicillamine 29-60 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 10353264-3 1999 Incubation with the NO donor S-nitroso-N-acetylpenicillamine (SNAP) for 24 hr increased IL-8 protein only in HaCaT cells, partly due to the presence of constitutive interleukin-1 (IL-1). S-Nitroso-N-Acetylpenicillamine 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 10466876-0 1999 Effect of an aluminum hydroxide-magnesium hydroxide combination drug on adhesion, IL-8 inducibility, and expression of HSP60 by Helicobacter pylori. Aluminum Hydroxide 13-31 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 10466876-0 1999 Effect of an aluminum hydroxide-magnesium hydroxide combination drug on adhesion, IL-8 inducibility, and expression of HSP60 by Helicobacter pylori. Magnesium Hydroxide 32-51 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 10466876-8 1999 IL-8 secretion from MKN45 cells after H. pylori infection was also inhibited by co-magaldrox. aluminum hydroxide, magnesium hydroxide, drug combination 80-92 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 10466876-10 1999 HSP60-induced IL-8 secretion was significantly inhibited by co-magaldrox in a dose-dependent manner. aluminum hydroxide, magnesium hydroxide, drug combination 60-72 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 10466876-11 1999 CONCLUSIONS: These results show that co-magaldrox suppressed the expression of the following virulence factors: adhesion, IL-8 inducibility, and expression of extracellular HSP60. aluminum hydroxide, magnesium hydroxide, drug combination 37-49 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 10358198-0 1999 Alcohol (ethanol) inhibits IL-8 and TNF: role of the p38 pathway. Alcohols 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 27-39 10358198-0 1999 Alcohol (ethanol) inhibits IL-8 and TNF: role of the p38 pathway. Ethanol 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 27-39 10358198-12 1999 Inhibition of IL-8 and TNF-alpha production by acute EtOH intoxication may inhibit inflammatory focused neutrophil migration and activation and may be a mechanism explaining the increased risk of trauma- and burn-related infections. Ethanol 53-57 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 10358198-8 1999 LPS-induced IL-8 and TNF-alpha production was inhibited in a similar pattern by pretreatment with either EtOH or SB202190 (1 microM), a specific inhibitor of p38 kinase. Ethanol 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 10445612-2 1999 To this end, the phosphorylation and activation of p38 MAP kinase and the effect of SB 203580, a specific inhibitor of p38 MAP kinase activity, on p38 MAP kinase activity and IL-8 expression in TNF-alpha- and IL-1alpha-stimulated human pulmonary vascular endothelial cells were examined. SB 203580 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 10357776-4 1999 Butyrate-induced expression of carcinoembryonic antigen and interleukin-8, dome formation and cell turnover were also markedly augmented by pre-treatment with phorbol myristate acetate. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 10357776-4 1999 Butyrate-induced expression of carcinoembryonic antigen and interleukin-8, dome formation and cell turnover were also markedly augmented by pre-treatment with phorbol myristate acetate. Tetradecanoylphorbol Acetate 159-184 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 10348816-0 1999 Helicobacter pylori-dependent ceramide production may mediate increased interleukin 8 expression in human gastric cancer cell lines. Ceramides 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 72-85 10348816-2 1999 Because several studies have shown that sphingolipids are involved in a number of signaling pathways, including NF-kappaB activation, we investigated the possible role of sphingolipids in the regulation of IL-8 expression in Kato III and AGS cells. Sphingolipids 171-184 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 10387004-0 1999 Disulfide bridges in interleukin-8 probed using non-natural disulfide analogues: dissociation of roles in structure from function. Disulfides 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 10387004-0 1999 Disulfide bridges in interleukin-8 probed using non-natural disulfide analogues: dissociation of roles in structure from function. Disulfides 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 10387004-1 1999 The structural and functional roles of the two disulfide bridges in interleukin-8 (IL-8) were addressed using IL-8 analogues with covalently modified disulfide bridges. Disulfides 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 10387004-1 1999 The structural and functional roles of the two disulfide bridges in interleukin-8 (IL-8) were addressed using IL-8 analogues with covalently modified disulfide bridges. Disulfides 47-56 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 10387004-1 1999 The structural and functional roles of the two disulfide bridges in interleukin-8 (IL-8) were addressed using IL-8 analogues with covalently modified disulfide bridges. Disulfides 150-159 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 10387004-1 1999 The structural and functional roles of the two disulfide bridges in interleukin-8 (IL-8) were addressed using IL-8 analogues with covalently modified disulfide bridges. Disulfides 150-159 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 10387004-6 1999 Modification to the disulfide bridge between cysteines 9 and 50 had only a modest effect on IL-8 function. Disulfides 20-29 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 10387004-6 1999 Modification to the disulfide bridge between cysteines 9 and 50 had only a modest effect on IL-8 function. Cysteine 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 10362718-11 1999 Immunoreactive leukotriene B4 receptor, interleukin-8, granulocyte colony-stimulating factor, and monocyte chemoattractant protein-1 significantly increased in supernatant fluids in response to bleomycin. Bleomycin 194-203 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 10333502-3 1999 However, fluoride ion (1 M NaF) causes a 1000-fold activation of the mutant enzyme while simultaneously inhibiting WT activity by 20-fold in the forward reaction. Fluorides 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 10401557-8 1999 Moreover, rolipram significantly potentiated hyperalgesia induced by carrageenan, bradykinin, TNF alpha, IL-1 beta, IL-6 and IL-8. Rolipram 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 10401557-15 1999 The ODQ potentiated hyperalgesia induced by carrageenan, bradykinin, TNF alpha, IL-1 beta, IL-6 and IL-8. 1H-(1,2,3)oxadiazolo(4,4-a)quinoxalin-1-one 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 10445614-8 1999 In conclusion, interleukin-8, neutrophil elastase and leukotriene B4 contribute to the neutrophilic inflammation in the airways of chronic lower respiratory tract infection patients and the clinical effects of roxithromycin may, in part, be attributable to the suppression of excess release of the chemotactic mediators from inflammatory cells. Roxithromycin 210-223 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 10348816-7 1999 RESULTS: A cell-permeable ceramide analogue (C2-ceramide) increased IL-8 expression with comparable mRNA induction. Ceramides 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10348816-7 1999 RESULTS: A cell-permeable ceramide analogue (C2-ceramide) increased IL-8 expression with comparable mRNA induction. N-acetylsphingosine 45-56 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10348816-8 1999 This effect was mimicked by sphingomyelinase, but not by phospholipase A2 or phospholipase C. C2-ceramide induced IL-8 gene transcription mainly through activation of NF-kappaB because mutation of the NF-kappaB-binding site completely abrogated the induction of luciferase activity. N-acetylsphingosine 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 10348816-10 1999 CONCLUSIONS: The results suggest a novel role of the sphingomyelin-ceramide pathway, at least in part through NF-kappaB, in IL-8 production induced by H. pylori infection in gastric epithelial cells. Sphingomyelins 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 10348816-10 1999 CONCLUSIONS: The results suggest a novel role of the sphingomyelin-ceramide pathway, at least in part through NF-kappaB, in IL-8 production induced by H. pylori infection in gastric epithelial cells. Ceramides 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 10445612-4 1999 Inhibition of TNF-alpha- and IL-1alpha-induced p38 MAP kinase activity by SB 203580 inhibited TNF-alpha- and IL-1alpha-induced IL-8 protein production as well as IL-8 messenger ribonucleic acid (mRNA) expression, indicating that SB 203580 was effective at the transcriptional level. SB 203580 74-83 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 10424432-4 1999 PD98059, an inhibitor of MAP kinase kinase (MEK), inhibited IL-6, IL-8 and basic FGF production in HS and all cytokines production except basic FGF in SW982. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 10424432-7 1999 Rolipram or R0201724, an inhibitor of cyclic AMP-specific PDE, inhibited IL-8 and basic FGF production in HS and TNFalpha production in SW982, however, it enhanced the other cytokines production in SW982. Cyclic AMP 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 10392761-6 1999 (S)- and (R)-ibuprofen were equal in their inhibitory/activating effects on cytokine production, with the exception of stronger IL-8 induction in endothelial cells by (R)-ibuprofen as compared to its chiral analogue. Ibuprofen 167-180 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 10359894-10 1999 Moreover, supernatants from DEP-PAH-activated cells, compared with those of controls, exhibited a significantly enhanced chemotactic activity for neutrophils and eosinophils, which was significantly inhibited by pretreatment with anti-IL-8 and anti-RANTES neutralizing antibodies, respectively. p-Aminohippuric Acid 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 235-239 10437657-0 1999 Inducer-specific bidirectional regulation of endothelial interleukin-8 production by thalidomide. Thalidomide 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 10454826-10 1999 Calcium mobilization experiments revealed minimal inhibition of the IL-8-induced increase in calcium after pretreatment with TNFalpha, but the response to NAP-2 was substantially inhibited. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10341002-4 1999 We also evaluated the mRNA expression for IL-6 and IL-8 in ESC after C-PAF stimulation using Northern blot analysis. 1-O-hexadecyl-2-N-methylcarbamol -sn-glycerol-3-phosphocholine 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 10454826-10 1999 Calcium mobilization experiments revealed minimal inhibition of the IL-8-induced increase in calcium after pretreatment with TNFalpha, but the response to NAP-2 was substantially inhibited. Calcium 93-100 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10226072-8 1999 Furthermore, we found significant increases in the release of IL-4, IL-6, IL-8, and TNF-alpha of ozone-exposed (0.1 ppm) samples of atopic versus nonatopic patients and to a lesser extent for histamine following exposure to 0.15 ppm ozone. Ozone 97-102 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 10216072-2 1999 Only a subgroup of CXC chemokines defined by the conserved sequence motif glutamic acid-leucine-arginine (ELR) tripeptide motif, which included interleukin-8 (IL-8), growth-regulated oncogene alpha (GROalpha), neutrophil-activating peptide-2 (NAP-2), and epithelial cell-derived neutrophil activating peptide-78 (ENA-78), induced calcium flux in the cells. elr 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 144-157 10216072-2 1999 Only a subgroup of CXC chemokines defined by the conserved sequence motif glutamic acid-leucine-arginine (ELR) tripeptide motif, which included interleukin-8 (IL-8), growth-regulated oncogene alpha (GROalpha), neutrophil-activating peptide-2 (NAP-2), and epithelial cell-derived neutrophil activating peptide-78 (ENA-78), induced calcium flux in the cells. tripeptide K-26 111-121 C-X-C motif chemokine ligand 8 Homo sapiens 144-157 10225834-3 1999 In contrast, PMNLs from the HIV and HIV/TB groups responded reciprocally in the same assay; that is, higher IL-8 input concentrations resulted in the release of less enzyme than lower IL-8 input concentrations. Terbium 40-42 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 10225834-3 1999 In contrast, PMNLs from the HIV and HIV/TB groups responded reciprocally in the same assay; that is, higher IL-8 input concentrations resulted in the release of less enzyme than lower IL-8 input concentrations. Terbium 40-42 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 10328874-4 1999 In addition, sodium salicylate and additional NSAIDs used at concentrations that activate HSF1 also inhibited the expression of other monocytic genes (TNF-alpha, IL-1beta, IL-6, IL-8, IL-10, ICAM-1) activated by exposure to a pro-inflammatory stimulus (lipopolysaccharide, LPS). Sodium Salicylate 13-30 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 10229865-13 1999 The concentrations of IL-8, G-CSF, monocyte chemoattractant protein-1, GM-CSF, and TGF-beta in the supernatant fluids significantly increased in response to bleomycin. Bleomycin 157-166 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 10326962-4 1999 RESULTS: Antazoline hydrochloride, emedastine difumarate, levocabastine hydrochloride, olopatadine hydrochloride, and pheniramine maleate attenuated histamine-stimulated phosphatidylinositol turnover and IL-6 and IL-8 secretion. Olopatadine Hydrochloride 87-112 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 10326962-4 1999 RESULTS: Antazoline hydrochloride, emedastine difumarate, levocabastine hydrochloride, olopatadine hydrochloride, and pheniramine maleate attenuated histamine-stimulated phosphatidylinositol turnover and IL-6 and IL-8 secretion. Pheniramine 118-137 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 10326962-4 1999 RESULTS: Antazoline hydrochloride, emedastine difumarate, levocabastine hydrochloride, olopatadine hydrochloride, and pheniramine maleate attenuated histamine-stimulated phosphatidylinositol turnover and IL-6 and IL-8 secretion. Histamine 149-158 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 10226715-1 1999 AIMS: The study aims to directly measure uptake of Na and F ions by glass ionomer cement from dilute NaF solution and compare this with the subsequent re-release of these ions into water. Fluorine 58-59 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 10226715-14 1999 CONCLUSIONS: Glass ionomer cements take up Na and F ions from NaF solution in large quantities and in equimolar proportion. Fluorine 50-51 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 10362412-0 1999 Effect of the nitric oxide inhibitor, L-N(G)-monomethylarginine, on accumulation of interleukin-6 and interleukin-8, and nuclear factor-kappaB activity in a human endothelial cell line. Nitric Oxide 14-26 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 10362412-0 1999 Effect of the nitric oxide inhibitor, L-N(G)-monomethylarginine, on accumulation of interleukin-6 and interleukin-8, and nuclear factor-kappaB activity in a human endothelial cell line. l-n(g)-monomethylarginine 38-63 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 10362412-7 1999 IL-6 accumulation was decreased (p < .05) and IL-8 accumulation increased (p < .01) with L-NMMA. N(G)-monomethylarginine acetate 95-101 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 10437388-5 1999 Histamine increases IL-8 level and evokes leukocyte rolling on endothelial cells. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 10329835-0 1999 Elevated levels of IL-8 in interstitial pneumonia induced by low-dose methotrexate. Methotrexate 70-82 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 10325294-1 1999 Hyaluronic acid (HA) stimulates the synthesis of interleukin (IL) 8, while dehydroepiandrosterone sulphate (DHEA-S) induces the expression of IL-8 and its receptor in the human cervical fibroblast. Hyaluronic Acid 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 49-67 10325294-1 1999 Hyaluronic acid (HA) stimulates the synthesis of interleukin (IL) 8, while dehydroepiandrosterone sulphate (DHEA-S) induces the expression of IL-8 and its receptor in the human cervical fibroblast. Hyaluronic Acid 17-19 C-X-C motif chemokine ligand 8 Homo sapiens 49-67 10325294-1 1999 Hyaluronic acid (HA) stimulates the synthesis of interleukin (IL) 8, while dehydroepiandrosterone sulphate (DHEA-S) induces the expression of IL-8 and its receptor in the human cervical fibroblast. Dehydroepiandrosterone Sulfate 75-106 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 10227335-0 1999 Grain dust induces IL-8 production from bronchial epithelial cells: the effect of dexamethasone on IL-8 production. Dexamethasone 82-95 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 10202011-7 1999 Finally, both N-acetylcysteine and pyrrolidine dithiocarbamate attenuated the action of DEP on IL-8 mRNA expression, suggesting that oxidant-mediated pathway might be involved in its processes. Acetylcysteine 14-30 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 10202011-7 1999 Finally, both N-acetylcysteine and pyrrolidine dithiocarbamate attenuated the action of DEP on IL-8 mRNA expression, suggesting that oxidant-mediated pathway might be involved in its processes. pyrrolidine dithiocarbamic acid 35-62 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 10369130-0 1999 Thrombin-induced interleukin-8 production and its regulation by interferon-gamma and prostaglandin E2 in human monocytic U937 cells. Dinoprostone 85-101 C-X-C motif chemokine ligand 8 Homo sapiens 17-30 10369130-6 1999 Moreover, thrombin-induced IL-8 production by U937 cells was differentially regulated by interferon (IFN)-gamma and prostaglandin (PG)E2. Dinoprostone 116-136 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 10103183-7 1999 Among these agents, imipenem demonstrated rapid killing of P. aeruginosa as well as rapid release of PNR and resulted in the highest IL-8 production. Imipenem 20-28 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 10103183-9 1999 The immunoprecipitates of the aliquots of bacterial culture containing imipenem or complement with anti-PNR immunoglobulin G (IgG) induced twofold-higher IL-8 production than did the immunoprecipitates of the aliquots of bacterial culture with a control IgG. Imipenem 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 10103198-3 1999 We studied the effect of erythromycin, clarithromycin, josamycin, and other antibiotics on the release by eosinophils of interleukin-8 (IL-8), a potent chemokine for inflammatory cells, including eosinophils themselves. Erythromycin 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 121-134 10227335-8 1999 RESULTS: There was significant production of IL-8 from bronchial epithelial cells with additions of GD in a dose-dependent manner (P < .05), which was significantly augmented with additions of PBMC supernatant (P < .05) at each concentration. Gadolinium 100-102 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 10103198-3 1999 We studied the effect of erythromycin, clarithromycin, josamycin, and other antibiotics on the release by eosinophils of interleukin-8 (IL-8), a potent chemokine for inflammatory cells, including eosinophils themselves. Erythromycin 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 10103198-3 1999 We studied the effect of erythromycin, clarithromycin, josamycin, and other antibiotics on the release by eosinophils of interleukin-8 (IL-8), a potent chemokine for inflammatory cells, including eosinophils themselves. Clarithromycin 39-53 C-X-C motif chemokine ligand 8 Homo sapiens 121-134 10227335-9 1999 Compared with the untreated sample, pretreatment of dexamethasone could induced a remarkable inhibitions (15% to 55%) of IL-8 production from bronchial epithelial cells in a dose-dependent manner. Dexamethasone 52-65 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 10103198-3 1999 We studied the effect of erythromycin, clarithromycin, josamycin, and other antibiotics on the release by eosinophils of interleukin-8 (IL-8), a potent chemokine for inflammatory cells, including eosinophils themselves. Clarithromycin 39-53 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 10227335-10 1999 CONCLUSION: These results suggest that IL-8 production from bronchial epithelial cells may contribute to neutrophil recruitment occurring in GD-induced airway inflammation. Gadolinium 141-143 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 10103198-3 1999 We studied the effect of erythromycin, clarithromycin, josamycin, and other antibiotics on the release by eosinophils of interleukin-8 (IL-8), a potent chemokine for inflammatory cells, including eosinophils themselves. Josamycin 55-64 C-X-C motif chemokine ligand 8 Homo sapiens 121-134 10103198-3 1999 We studied the effect of erythromycin, clarithromycin, josamycin, and other antibiotics on the release by eosinophils of interleukin-8 (IL-8), a potent chemokine for inflammatory cells, including eosinophils themselves. Josamycin 55-64 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 10227335-11 1999 The downregulation of IL-8 production by dexamethasone from bronchial epithelial cells may contribute to the efficacy of this compound in reducing cellular infiltration and ultimately to its anti-inflammatory property. Dexamethasone 41-54 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 10103198-5 1999 Only 14-member macrolides (erythromycin and clarithromycin) showed a concentration-dependent suppressive effect on IL-8 release (control, 100%; erythromycin at 1 microgram/ml, 67.82% +/- 3.45% [P < 0.01]; clarithromycin at 5 micrograms/ml, 56.81% +/- 9.61% [P < 0.01]). Erythromycin 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 10090924-8 1999 In addition, while treatment of neutrophils with LPS and TNF-alpha inhibited IL-8 receptor-mediated calcium mobilization and IL-8-directed neutrophil chemotaxis, both 1, 10-phenanthroline and EDTA blocked these inhibitory processes. 1,10-phenanthroline 167-187 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 10103198-5 1999 Only 14-member macrolides (erythromycin and clarithromycin) showed a concentration-dependent suppressive effect on IL-8 release (control, 100%; erythromycin at 1 microgram/ml, 67.82% +/- 3.45% [P < 0.01]; clarithromycin at 5 micrograms/ml, 56.81% +/- 9.61% [P < 0.01]). Clarithromycin 44-58 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 10103198-5 1999 Only 14-member macrolides (erythromycin and clarithromycin) showed a concentration-dependent suppressive effect on IL-8 release (control, 100%; erythromycin at 1 microgram/ml, 67.82% +/- 3.45% [P < 0.01]; clarithromycin at 5 micrograms/ml, 56.81% +/- 9.61% [P < 0.01]). Erythromycin 144-156 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 10090924-8 1999 In addition, while treatment of neutrophils with LPS and TNF-alpha inhibited IL-8 receptor-mediated calcium mobilization and IL-8-directed neutrophil chemotaxis, both 1, 10-phenanthroline and EDTA blocked these inhibitory processes. Calcium 100-107 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 10090924-8 1999 In addition, while treatment of neutrophils with LPS and TNF-alpha inhibited IL-8 receptor-mediated calcium mobilization and IL-8-directed neutrophil chemotaxis, both 1, 10-phenanthroline and EDTA blocked these inhibitory processes. Edetic Acid 192-196 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 10090924-8 1999 In addition, while treatment of neutrophils with LPS and TNF-alpha inhibited IL-8 receptor-mediated calcium mobilization and IL-8-directed neutrophil chemotaxis, both 1, 10-phenanthroline and EDTA blocked these inhibitory processes. Edetic Acid 192-196 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 10223179-6 1999 In contrast, the cell lines significantly increased alkaline phosphatase activities by >50%, urokinase receptor expression >2-fold and interleukin-8 secretion >3-fold in response to butyrate. Butyrates 191-199 C-X-C motif chemokine ligand 8 Homo sapiens 141-154 10223179-8 1999 Interleukin-8 secretion increased by 145 +/- 23% and 132 +/- 17% on 24 h exposure to 2 mM butyrate or 0.1 microM TNF alpha alone, respectively. Butyrates 90-98 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 10101223-6 1999 The membrane spanning heptahelical IL-8 receptor is coupled with the effector enzyme(s) through the intermediacy of heterotrimeric GTP-binding regulatory proteins. Guanosine Triphosphate 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 10101223-10 1999 Neutrophils activation of phospholipase D (PLD) and superoxide generation in response to IL-8 have also been demonstrated. Superoxides 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 10101223-11 1999 Furthermore, IL-8-mediated activation of mitogen activating protein kinase (MAPK) and tyrosine phosphorylation of cellular proteins have been observed. Tyrosine 86-94 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 10230950-8 1999 MEASUREMENTS AND MAIN RESULTS: After CPB, the concentration of the proinflammatory cytokines, interleukin-6 and interleukin-8, was significantly less in the methylprednisolone group. Methylprednisolone 157-175 C-X-C motif chemokine ligand 8 Homo sapiens 112-125 10211881-10 1999 In animals treated with AdvIL-10, the MMP-3-TIMP-1 balance was partially restored, independent of the effect on mRNA expression of tumor necrosis factor a, IL-1, IL-6, or IL-8. advil-10 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 10084995-5 1999 S. sanguis and S. mutans LTAs at a 1,000-fold excess each completely inhibited the IL-8-inducing activities of both LPS and a synthetic lipid A on CD14(high) HGF. Lipid A 136-143 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 10101031-11 1999 These results indicate that extracellular adenosine can regulate ERK, c-Jun N-terminal kinase, and p38 MAPK signaling cascades and that activation of ERK and p38 MAPK pathways are essential steps in adenosine A2B receptor-dependent stimulation of IL-8 production in HMC-1. Adenosine 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 10329481-0 1999 A potent immunosuppressant FK506 inhibits IL-8 expression in human eosinophils. Tacrolimus 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 10329481-3 1999 In the present study, we evaluated if FK506 had any effect on the production of IL-8, one of the important chemokines for a variety of inflammatory cells, from human peripheral eosinophils. Tacrolimus 38-43 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 10329481-4 1999 Purified eosinophils constitutively released IL-8, which was increased with calcium ionophore (10(-6) M). Calcium 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 10329481-5 1999 FK506 showed a dose-dependent suppressive effect on IL-8 production by eosinophils stimulated with calcium ionophore, but showed no effect on unstimulated cells. Tacrolimus 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 10329481-5 1999 FK506 showed a dose-dependent suppressive effect on IL-8 production by eosinophils stimulated with calcium ionophore, but showed no effect on unstimulated cells. Calcium 99-106 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 10329481-6 1999 Evaluation of IL-8 mRNA levels by reverse transcription and polymerase chain reaction demonstrated that FK506 suppressed IL-8 gene expression only in activated eosinophils. Tacrolimus 104-109 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 10329481-6 1999 Evaluation of IL-8 mRNA levels by reverse transcription and polymerase chain reaction demonstrated that FK506 suppressed IL-8 gene expression only in activated eosinophils. Tacrolimus 104-109 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 10101031-4 1999 The mechanism by which adenosine promotes IL-8 synthesis has not been defined. Adenosine 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 10076137-0 1999 The action of prostaglandin E2 on the human cervix: stimulation of interleukin 8 and inhibition of secretory leukocyte protease inhibitor. Dinoprostone 14-30 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 10367558-5 1999 Lithium (10(-3) M) significantly increased the unstimulated production of IL-8 and IL-10. Lithium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 10367558-6 1999 CONCLUSIONS: The results suggest that lithium has significant immunoregulatory effects by increasing the production of both proinflammatory cytokines (IFNgamma, TNFalpha and IL-8) and negative immunoregulatory cytokines or proteins (IL-10 and the IL-1RA). Lithium 38-45 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 10363611-15 1999 CONCLUSIONS: The results show a similar reduction of the inflammatory cytokine release (IL-6 and IL-8 as markers) using early steroid application and aprotinin in high dosage. Steroids 126-133 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10076137-5 1999 RESULTS: Interleukin 8 release from cervical explants was stimulated by prostaglandin E2 and nitric oxide and inhibited by progesterone and dexamethasone. Dinoprostone 72-88 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 10076137-5 1999 RESULTS: Interleukin 8 release from cervical explants was stimulated by prostaglandin E2 and nitric oxide and inhibited by progesterone and dexamethasone. Nitric Oxide 93-105 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 10076137-5 1999 RESULTS: Interleukin 8 release from cervical explants was stimulated by prostaglandin E2 and nitric oxide and inhibited by progesterone and dexamethasone. Progesterone 123-135 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 10076137-5 1999 RESULTS: Interleukin 8 release from cervical explants was stimulated by prostaglandin E2 and nitric oxide and inhibited by progesterone and dexamethasone. Dexamethasone 140-153 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 10191034-10 1999 A significant increase of interleukin-8 release could be found after 4 h of rew/reox following storage in EuroCollins solution. eurocollins 106-117 C-X-C motif chemokine ligand 8 Homo sapiens 26-39 10204985-0 1999 Hydrolysis of alpha-tricalcium phosphate in NaF solutions. alpha-tricalcium phosphate 14-40 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 10204985-3 1999 Hydrolysis of alpha-tricalcium phosphate (alpha-TCP) was carried out at physiologic temperature in NaF solutions and the solids product(s) were analyzed. alpha-tricalcium phosphate 14-40 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 10204985-3 1999 Hydrolysis of alpha-tricalcium phosphate (alpha-TCP) was carried out at physiologic temperature in NaF solutions and the solids product(s) were analyzed. alpha-tricalcium phosphate 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 10204985-7 1999 The extent of fluoride and sodium incorporation in the apatites formed varied depending on the NaF concentration of the solution. Fluorides 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 10204985-7 1999 The extent of fluoride and sodium incorporation in the apatites formed varied depending on the NaF concentration of the solution. Sodium 27-33 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 10342040-1 1999 OBJECTIVES: The aim of this study was to investigate the effects of two nonsteroidal anti-inflammatory drugs (NSAIDs), nimesulide and sodium diclofenac, on the production of proteoglycans (PG), prostaglandin E2 (PGE2) and cytokines (IL-6 and IL-8) by human articular chondrocytes in vitro. nimesulide 119-129 C-X-C motif chemokine ligand 8 Homo sapiens 242-246 10342040-1 1999 OBJECTIVES: The aim of this study was to investigate the effects of two nonsteroidal anti-inflammatory drugs (NSAIDs), nimesulide and sodium diclofenac, on the production of proteoglycans (PG), prostaglandin E2 (PGE2) and cytokines (IL-6 and IL-8) by human articular chondrocytes in vitro. Diclofenac 134-151 C-X-C motif chemokine ligand 8 Homo sapiens 242-246 10204985-11 1999 The (Ca+Na)/P ratio of the apatite formed by alpha-TCP hydrolysis in 0.1M NaF approaches 1.67 indicating the vacant Ca sites become almost completely filled by the Na ions. ca+na 5-10 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 10204985-11 1999 The (Ca+Na)/P ratio of the apatite formed by alpha-TCP hydrolysis in 0.1M NaF approaches 1.67 indicating the vacant Ca sites become almost completely filled by the Na ions. alpha-tricalcium phosphate 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 10199534-13 1999 CONCLUSIONS: Methylprednisolone reduces the production of IL-6 and IL-8 but not that of IL-10 and IL-1ra. Methylprednisolone 13-31 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 10092093-3 1999 Here, we have measured IL-8-induced Ca2+ signals in single human neutrophil granulocytes using the Ca2+ indicator dye FURA-2 AM and we have investigated the signal transduction that leads to these Ca2+ signals with various pharmacological tools. fura-2-am 118-127 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 10213368-11 1999 Microparticles prepared from either chitosan or starch microparticles, applied apically, induced the basolateral release of IL-6 and IL-8 from polarized Calu-3 cells. Chitosan 36-44 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 10080530-3 1999 Our results demonstrate that H2O2 induction of IL-8 gene expression is linked with the selective binding of AP-1 to the IL-8 promoter, whereas TNF-alpha and RSV induction of IL-8 correlates with the activation of NF-kappaB binding. Hydrogen Peroxide 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 10080530-3 1999 Our results demonstrate that H2O2 induction of IL-8 gene expression is linked with the selective binding of AP-1 to the IL-8 promoter, whereas TNF-alpha and RSV induction of IL-8 correlates with the activation of NF-kappaB binding. Hydrogen Peroxide 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 10080530-3 1999 Our results demonstrate that H2O2 induction of IL-8 gene expression is linked with the selective binding of AP-1 to the IL-8 promoter, whereas TNF-alpha and RSV induction of IL-8 correlates with the activation of NF-kappaB binding. Hydrogen Peroxide 29-33 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 10089966-0 1999 Inhibitory effect of erythromycin on interleukin-8 secretion from exudative cells in the nasal discharge of patients with chronic sinusitis. Erythromycin 21-33 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 10089966-2 1999 The authors studied the inhibitory effect of erythromycin on interleukin-8 (IL-8) secretion from exudative cells in the nasal discharge of patients with chronic sinusitis. Erythromycin 45-57 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 10089966-2 1999 The authors studied the inhibitory effect of erythromycin on interleukin-8 (IL-8) secretion from exudative cells in the nasal discharge of patients with chronic sinusitis. Erythromycin 45-57 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 10089966-6 1999 RESULTS: The amount of secreted IL-8 in the absence of erythromycin was 682 +/- 226 pg/10(6) cells/24 h. The IL-8 secretion was significantly reduced to 66 +/- 15% and 46 +/- 13% of the control in the presence of 10(-6) and 10(-5) M of erythromycin, respectively. Erythromycin 55-67 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 10089966-6 1999 RESULTS: The amount of secreted IL-8 in the absence of erythromycin was 682 +/- 226 pg/10(6) cells/24 h. The IL-8 secretion was significantly reduced to 66 +/- 15% and 46 +/- 13% of the control in the presence of 10(-6) and 10(-5) M of erythromycin, respectively. Erythromycin 236-248 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 10089966-7 1999 CONCLUSION: Erythromycin may act as a biologic modulator that inhibits IL-8 secretion from exudative cells and thereby blocks the vicious circle of neutrophil recruitment and IL-8 generation in the inflammatory site in chronic sinusitis. Erythromycin 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 10089966-7 1999 CONCLUSION: Erythromycin may act as a biologic modulator that inhibits IL-8 secretion from exudative cells and thereby blocks the vicious circle of neutrophil recruitment and IL-8 generation in the inflammatory site in chronic sinusitis. Erythromycin 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 10333355-7 1999 SPF, PGE2 and 19-hydroxy PGE significantly (P< 0.005) stimulated IL-8 release from peripheral blood and U937 cells. butylparaben 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10333355-7 1999 SPF, PGE2 and 19-hydroxy PGE significantly (P< 0.005) stimulated IL-8 release from peripheral blood and U937 cells. Dinoprostone 5-9 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10333355-7 1999 SPF, PGE2 and 19-hydroxy PGE significantly (P< 0.005) stimulated IL-8 release from peripheral blood and U937 cells. 19-hydroxy pge 14-28 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10333355-8 1999 19-hydroxy PGE was significantly (P< 0.005) more effective than PGE2 in stimulating IL-8 release. 19-hydroxy pge 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 10333355-8 1999 19-hydroxy PGE was significantly (P< 0.005) more effective than PGE2 in stimulating IL-8 release. Dinoprostone 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 10213368-11 1999 Microparticles prepared from either chitosan or starch microparticles, applied apically, induced the basolateral release of IL-6 and IL-8 from polarized Calu-3 cells. Starch 48-54 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 10050881-0 1999 Regulation of interleukin-8 expression by reduced oxygen pressure in human glioblastoma. Oxygen 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 10076615-10 1999 There was a significant negative correlation between the peak serum IL-8 level and the initial velocity of arterial ketone body ratio recovery for the first 5 minutes after reperfusion r = -0.83, P < .001). Ketones 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 10050881-9 1999 Since intratumoral augmentation of IL-8 and VEGF secretion, following microenvironmental decreases in oxygen pressure, may promote angiogenesis, further definition of these pathways is essential to appropriately target them for antitumoral therapy. Oxygen 102-108 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 10368283-9 1999 In this model, the heparin-binding residues of IL-8 are exposed, thereby allowing presentation of the chemokine from endothelial cell-surface glycosaminoglycans. Heparin 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 10368283-9 1999 In this model, the heparin-binding residues of IL-8 are exposed, thereby allowing presentation of the chemokine from endothelial cell-surface glycosaminoglycans. Glycosaminoglycans 142-160 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 10063910-6 1999 Externally applied H2O2 significantly up-regulated IL-8 expression. Hydrogen Peroxide 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 9927384-5 1999 SB 203580 as the specific p38 MAP kinase inhibitor inhibited hyperosmolarity-induced p38 MAP kinase activation and partially inhibited hyperosmolarity-induced IL-8 expression. SB 203580 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 10048791-0 1999 Formation of phosphatidic acid and subclasses of phosphatidylethanol in human neutrophils upon interleukin-8 stimulation. Phosphatidic Acids 13-30 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 10048791-0 1999 Formation of phosphatidic acid and subclasses of phosphatidylethanol in human neutrophils upon interleukin-8 stimulation. phosphatidylethanol 49-68 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 10048791-1 1999 Previous studies showed that interleukin-8 (IL-8) stimulates phospholipase D hydrolysis of phosphatidylcholine to generate phosphatidic acid in human neutrophils. Phosphatidylcholines 91-110 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 10048791-1 1999 Previous studies showed that interleukin-8 (IL-8) stimulates phospholipase D hydrolysis of phosphatidylcholine to generate phosphatidic acid in human neutrophils. Phosphatidylcholines 91-110 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 10048791-1 1999 Previous studies showed that interleukin-8 (IL-8) stimulates phospholipase D hydrolysis of phosphatidylcholine to generate phosphatidic acid in human neutrophils. Phosphatidic Acids 123-140 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 10048791-1 1999 Previous studies showed that interleukin-8 (IL-8) stimulates phospholipase D hydrolysis of phosphatidylcholine to generate phosphatidic acid in human neutrophils. Phosphatidic Acids 123-140 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 10048791-3 1999 No studies have examined phospholipase D hydrolysis of the three subclasses of phosphatidylcholine in interleukin-8-stimulated neutrophils. Phosphatidylcholines 79-98 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 10048791-7 1999 Our findings suggest that phospholipase D catalyses the hydrolysis of diacyl, alkylacyl and alkenylacyl subclasses of phosphatidylcholine in neutrophils upon IL-8 stimulation. Phosphatidylcholines 118-137 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 10063906-0 1999 Helicobacter pylori water extract induces interleukin-8 production by gastric epithelial cells. Water 20-25 C-X-C motif chemokine ligand 8 Homo sapiens 42-55 10063906-3 1999 The aims of the present study were to determine whether an H. pylori water extract (HPE) induces IL-8 production by gastric epithelial cells and to characterize IL-8-inducing substances in HPE. Water 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 10063910-5 1999 N-Acetylcysteine (NAC) or dimethylsulfoxide inhibited IL-8 expression induced by tumor necrosis factor-alpha (TNF-alpha) or interleukin-1beta (IL-1beta). Acetylcysteine 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 10063910-5 1999 N-Acetylcysteine (NAC) or dimethylsulfoxide inhibited IL-8 expression induced by tumor necrosis factor-alpha (TNF-alpha) or interleukin-1beta (IL-1beta). Acetylcysteine 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 10063910-5 1999 N-Acetylcysteine (NAC) or dimethylsulfoxide inhibited IL-8 expression induced by tumor necrosis factor-alpha (TNF-alpha) or interleukin-1beta (IL-1beta). Dimethyl Sulfoxide 26-43 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9916078-5 1999 By using PD-98059 and SB203580, two potent and selective inhibitors of MEK1 (a kinase upstream of ERK1/2) and p38, respectively, we have demonstrated that both ERK1/2 and p38 cascades play a key role in the production of IL-8 by monocytes and PMN stimulated with bacterial fractions. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 9895238-4 1999 N-acetyl cysteine inhibited RV-induced NF-kappaB activation and IL-8 elaboration. Acetylcysteine 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 9916078-5 1999 By using PD-98059 and SB203580, two potent and selective inhibitors of MEK1 (a kinase upstream of ERK1/2) and p38, respectively, we have demonstrated that both ERK1/2 and p38 cascades play a key role in the production of IL-8 by monocytes and PMN stimulated with bacterial fractions. SB 203580 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 10069413-0 1999 Inhibition of IL-6 and IL-8 induction from cultured rheumatoid synovial fibroblasts by treatment with aurothioglucose. Aurothioglucose 102-117 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 10069413-3 1999 In this study, we examined the effect of one of the monovalent gold compounds, aurothioglucose (AuTG), on the IL-1-induced production of IL-6, IL-8 and granulocyte macrophage colony stimulating factor (GM-CSF) from rheumatoid synovial fibroblasts (RSF) isolated from three RA patients. Aurothioglucose 79-94 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 10337430-19 1999 (7) have shown that exposure of human conjunctival epithelial cells to histamine leads to the production of pro-inflammatory cytokines IL-6 and IL-8. Histamine 71-80 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 10069413-4 1999 IL-6 and IL-8 induction but not GM-CSF induction was inhibited in most of the RSF after pretreatment with AuTG. (3r,3as,6ar)-Hexahydrofuro[2,3-B]furan-3-Ol 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 10069413-4 1999 IL-6 and IL-8 induction but not GM-CSF induction was inhibited in most of the RSF after pretreatment with AuTG. Aurothioglucose 106-110 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 10380161-7 1999 In the BL, NO2 exposure caused increases in polymorphonuclear neutrophils (PMNs), interleukin 6 (IL-6), IL-8, alpha1-antitrypsin, and tissue plasminogen activator, and decreases in epithelial cells. Nitrogen Dioxide 11-14 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 9973432-5 1999 In contrast, inhibition of IL-8 and GRO activities using neutralizing Abs resulted in a specific 6-fold increase in PGE2 but not in PGF2alpha production by stimulated microglial cells and astrocytes, whereas Abs to beta-chemokines had no effect. Dinoprostone 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9973432-8 1999 Conversely, the elevated intracerebral alpha-chemokine levels could reduce PG secretion, preventing the exacerbation of inflammation and neurotoxicity. Prostaglandins 75-77 C-X-C motif chemokine ligand 8 Homo sapiens 39-54 9927048-9 1999 In MM-1 and MM-2 cells, IL-8 caused a dose-dependent increase of [3H]thymidine incorporation to maximal levels of 46.3 +/- 3.6% and 12.3 +/- 1.6% (P < 0.001), respectively, when compared with serum-free medium as control. Tritium 66-68 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 10022397-6 1999 Compared with controls (IL-6, 1.1 +/- 0.3 ng/L; IL-8, 3.2 +/- 0.8 ng/L), untreated patients with GD and TNG had elevated IL-6 (GD, 7.11 +/- 0.88 ng/L; TNG, 7.30 +/- 0.77 ng/L; P < 0.001) and IL-8 (GD, 10.3 +/- 1.23 ng/L; TNG, 9.81 +/- 1.27 ng/L; P < 0.001). Nitroglycerin 104-107 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 10022397-8 1999 Thyroid carcinoma patients on TSH suppressive therapy also had significantly raised levels of IL-6 (2.5 +/- 0.42 ng/L) and IL-8 (4.4 +/- 0.63 ng/L). Thyrotropin 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 10191628-4 1999 Flow cytometric detection of intracellular cytokines in tonsillar mononuclear cells stimulated with PMA and ionomycin revealed that CD3 cells produced IL-1 alpha, IL-2, IL-4, IL-8, IFN-gamma and TNF-alpha, and CD19 cells produced IL-1 alpha, IL-6, IL-8 and TFN-alpha. Tetradecanoylphorbol Acetate 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 10191628-4 1999 Flow cytometric detection of intracellular cytokines in tonsillar mononuclear cells stimulated with PMA and ionomycin revealed that CD3 cells produced IL-1 alpha, IL-2, IL-4, IL-8, IFN-gamma and TNF-alpha, and CD19 cells produced IL-1 alpha, IL-6, IL-8 and TFN-alpha. Tetradecanoylphorbol Acetate 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 248-252 10191628-4 1999 Flow cytometric detection of intracellular cytokines in tonsillar mononuclear cells stimulated with PMA and ionomycin revealed that CD3 cells produced IL-1 alpha, IL-2, IL-4, IL-8, IFN-gamma and TNF-alpha, and CD19 cells produced IL-1 alpha, IL-6, IL-8 and TFN-alpha. Ionomycin 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 9918530-0 1999 Interleukin-8 mediates downregulation of tissue inhibitor of metalloproteinase-1 expression in cholesterol-loaded human macrophages: relevance to stability of atherosclerotic plaque. Cholesterol 95-106 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9916736-5 1999 While actinomycin-D (1 microg/ml) had little influence on the generation of IL-8 during chemotaxis, the protein synthesis inhibitor cycloheximide (10 microg/ml) markedly blunted the accumulation of cell-associated IL-8, suggesting that new protein synthesis from preexisting mRNA was responsible for the effect. Cycloheximide 132-145 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 9916736-6 1999 Consistent with this interpretation, migrating cells incorporated over 10 times as much [3H]leucine into IL-8 as did nonmotile neutrophils exposed to chemoattractants. Tritium 89-91 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 9916736-6 1999 Consistent with this interpretation, migrating cells incorporated over 10 times as much [3H]leucine into IL-8 as did nonmotile neutrophils exposed to chemoattractants. Leucine 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 10483873-8 1999 We also found that fraxiparine was able to significantly increase chemokinesis and decrease chemotaxis in the gradient of both fMLP and IL-8. Nadroparin 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 9864200-5 1999 When gentamicin was added to INT407 cells at 2 h after infection with 81-176, IL-8 secretion 22 h later was equivalent to that of controls without gentamicin, suggesting that the events which trigger induction and release of IL-8 occur early in the interactions of bacteria and eukaryotic cells. Gentamicins 5-15 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 10505790-0 1999 Nitric oxide regulates interleukin-8 gene expression in activated endothelium by inhibiting NF-kappaB binding to DNA: effects on endothelial function. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 10505790-2 1999 We showed that exogenous nitric oxide in the form of a nitric oxide donor significantly reduced IL-8 mRNA in cytokine-activated ECV304. Nitric Oxide 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 10505790-2 1999 We showed that exogenous nitric oxide in the form of a nitric oxide donor significantly reduced IL-8 mRNA in cytokine-activated ECV304. Nitric Oxide 55-67 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 10505790-3 1999 Similarly, nitric oxide significantly reduced migration of polymorphonuclear neutrophils through cytokine-activated ECV304 monolayers, an IL-8-dependent process. Nitric Oxide 11-23 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 10505790-4 1999 Using a luciferase reporter construct containing the NF-kappaB site of the IL-8 gene, we showed that exposing cytokine-activated ECV304 to exogenous nitric oxide resulted in significant reduction of NF-kappaB binding. Nitric Oxide 149-161 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9892783-4 1999 This was tested by measuring the effect of sodium fluoride (NaF) on cytokine production by human whole blood cells stimulated in vitro. Sodium Fluoride 43-58 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 10051702-11 1999 The amount of IL-8 and GM-CSF, induced by histamine, was significantly higher in DEP extract pretreated HNECs and HMMECs than nontreated HNECs and HMMECs. Histamine 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 10051702-12 1999 CONCLUSION: These results strongly suggest that DEP accelerates the inflammatory change by not only directly upregulating H1R expression but also increasing histamine-induced IL-8 and GM-CSF production. Histamine 157-166 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 9864200-5 1999 When gentamicin was added to INT407 cells at 2 h after infection with 81-176, IL-8 secretion 22 h later was equivalent to that of controls without gentamicin, suggesting that the events which trigger induction and release of IL-8 occur early in the interactions of bacteria and eukaryotic cells. Gentamicins 5-15 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 9950270-8 1999 The present IL-8 dependent and cAMP-regulated augmentation of LPS-induced stimulation of transmigration is the first description of an additive effect of PTX with a pro-inflammatory agent. Pentoxifylline 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 10092202-0 1999 Effects of erythromycin and its derivatives on interleukin-8 release by human bronchial epithelial cell line BEAS-2B cells. Erythromycin 11-23 C-X-C motif chemokine ligand 8 Homo sapiens 47-60 10702726-7 1999 Induction of oxidative stress by H(2)O(2) upregulated IL-8 expression. Hydrogen Peroxide 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 10702726-9 1999 ISIS 2922 only partially inhibited the upregulation of IL-8 in infected cells treated with H(2)O(2), whereas cotreatment with ISIS 2922 and antioxidants inhibited the upregulation almost completely. Water 91-96 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 10080106-0 1999 Acute alcohol consumption attenuates interleukin-8 (IL-8) and monocyte chemoattractant peptide-1 (MCP-1) induction in response to ex vivo stimulation. Alcohols 6-13 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 10080106-0 1999 Acute alcohol consumption attenuates interleukin-8 (IL-8) and monocyte chemoattractant peptide-1 (MCP-1) induction in response to ex vivo stimulation. Alcohols 6-13 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 9920091-1 1999 The role of progesterone (P4) in the regulation of inflammatory mediators interleukin-8 (IL-8), monocyte chemoattractant protein-1, and cyclooxygenase-2 (COX-2) and in the recruitment of leukocyte subpopulations in the endometrium has been examined, by employing a model of P4 withdrawal and maintenance in vivo. Progesterone 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 9920091-1 1999 The role of progesterone (P4) in the regulation of inflammatory mediators interleukin-8 (IL-8), monocyte chemoattractant protein-1, and cyclooxygenase-2 (COX-2) and in the recruitment of leukocyte subpopulations in the endometrium has been examined, by employing a model of P4 withdrawal and maintenance in vivo. Progesterone 12-24 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 10414594-13 1999 In untreated subjects and in patients receiving NaF, the former fraction contains ionic fluoride. Fluorides 88-96 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 9932682-10 1999 RESULTS: Postinjury PMNs were primed for both platelet-activating factor/N-formyl-methionyl-leucyl-phenylalanine-stimulated and lipopolysaccharide-stimulated IL-8 and TNF release at 2 hours after injury (fourfold increase of IL-8 release and fivefold increase of TNF release), whereas elective surgical patients demonstrated no priming. Nitrogen 22-23 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 9862763-3 1999 The increased production of IL-8 and expression of IL-8 mRNA were significantly inhibited by rebamipide (100-1000 microM) in a concentration-dependent manner. rebamipide 93-103 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 9862763-3 1999 The increased production of IL-8 and expression of IL-8 mRNA were significantly inhibited by rebamipide (100-1000 microM) in a concentration-dependent manner. rebamipide 93-103 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 9862763-7 1999 It is concluded that rebamipide exerts its preventive effect against H. pylori-evoked gastric mucosal cell inflammation by inhibition of the neutrophil adherence to the endothelial cells as well as by suppressing the surface expression of CD11b on neutrophils and the production of proinflammatory cytokine such as IL-8 from gastric epithelial cells. rebamipide 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 315-319 9932682-10 1999 RESULTS: Postinjury PMNs were primed for both platelet-activating factor/N-formyl-methionyl-leucyl-phenylalanine-stimulated and lipopolysaccharide-stimulated IL-8 and TNF release at 2 hours after injury (fourfold increase of IL-8 release and fivefold increase of TNF release), whereas elective surgical patients demonstrated no priming. Nitrogen 22-23 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 9835634-8 1999 These results suggest that inhaled steroids improve airway inflammation and lung function in asthmatics, presumably in part by inhibiting the synthesis of inflammatory cytokines such as IL-8 and GM-CSF. Steroids 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 12938511-1 1999 The effect of Sinomenine on IL-8, IL-6, IL-2 and mIL-2R produced by peripheral blood mononuclear cells was investigated by using cell culture, radioimmunoassay and flow cytometry. sinomenine 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 9888410-10 1999 RESULTS: There was a significant decrease in monocyte TNF, IL-8, and IL-6 production after OTZ therapy. otz 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 10348705-0 1999 Epinephrine promotes IL-8 production in human leukocytes via an effect on platelets. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 10413893-1 1999 According to previous pharmacokinetic studies the bioavailability of fluorine (F) from sodium monofluorophosphate (MFP) doubles that of sodium fluoride (NaF). Fluorine 69-77 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 10413893-1 1999 According to previous pharmacokinetic studies the bioavailability of fluorine (F) from sodium monofluorophosphate (MFP) doubles that of sodium fluoride (NaF). Sodium Fluoride 136-151 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 10440571-1 1999 We investigated the effect of FUT-175, a serine protease inhibitor, on the production of pro-inflammatory cytokines, interleukin-6 (IL-6) and interleukin-8 (IL-8), by monocytes stimulated with lipopolysaccharide (LPS). nafamostat 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 142-155 10440571-1 1999 We investigated the effect of FUT-175, a serine protease inhibitor, on the production of pro-inflammatory cytokines, interleukin-6 (IL-6) and interleukin-8 (IL-8), by monocytes stimulated with lipopolysaccharide (LPS). nafamostat 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 10325585-2 1999 Ethanol (EtOH) may play a role in the pathogenesis of psoriasis by upregulating the expression and inducing the local secretion of proinflammatory cytokines, e.g. interleukins IL-1alpha, IL-6, chemokine IL-8 and tumor necrosis factor alpha (TNF-alpha). Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 10325585-2 1999 Ethanol (EtOH) may play a role in the pathogenesis of psoriasis by upregulating the expression and inducing the local secretion of proinflammatory cytokines, e.g. interleukins IL-1alpha, IL-6, chemokine IL-8 and tumor necrosis factor alpha (TNF-alpha). Ethanol 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 10051376-5 1999 Curcumin inhibited the production of IL-8, MIP-1alpha, MCP-1, IL-1beta, and TNF-alpha by PMA- or LPS-stimulated monocytes and alveolar macrophages in a concentration- and a time-dependent manner. Curcumin 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 10051376-5 1999 Curcumin inhibited the production of IL-8, MIP-1alpha, MCP-1, IL-1beta, and TNF-alpha by PMA- or LPS-stimulated monocytes and alveolar macrophages in a concentration- and a time-dependent manner. Tetradecanoylphorbol Acetate 89-92 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 10051376-6 1999 These results show that curcumin exhibits an inhibitory effect on the production of IL-8, MIP-1alpha, MCP-1, IL-1beta, and TNF-alpha by PMA- or LPS-stimulated monocytes and alveolar macrophages. Curcumin 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9882597-3 1999 BEAS-2B cells, exposed to residual oil fly ash particles (ROFA), responded with an immediate (<30 s) increase in intracellular calcium levels ([Ca2+]i), increases of key inflammatory cytokine transcripts (i.e., IL-6, IL-8, TNFalpha) within 2 h exposure, and subsequent release of IL-6 and IL-8 cytokine protein after 4 h exposure. Oils 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 220-224 9882597-3 1999 BEAS-2B cells, exposed to residual oil fly ash particles (ROFA), responded with an immediate (<30 s) increase in intracellular calcium levels ([Ca2+]i), increases of key inflammatory cytokine transcripts (i.e., IL-6, IL-8, TNFalpha) within 2 h exposure, and subsequent release of IL-6 and IL-8 cytokine protein after 4 h exposure. Oils 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 292-296 9882597-5 1999 However, pretreatment of these cells with capsazepine (CPZ), an antagonist for capsaicin (i.e., vanilloid) receptors, inhibited the immediate increases in [Ca2+]i, diminished transcript (i.e., IL-6, IL-8, TNFalpha) levels and reduced IL-6 cytokine release to control levels. capsazepine 42-53 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 9882597-5 1999 However, pretreatment of these cells with capsazepine (CPZ), an antagonist for capsaicin (i.e., vanilloid) receptors, inhibited the immediate increases in [Ca2+]i, diminished transcript (i.e., IL-6, IL-8, TNFalpha) levels and reduced IL-6 cytokine release to control levels. capsazepine 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 9882597-6 1999 BEAS-2B cells exposed to ROFA in calcium-free media failed to demonstrate increases of [Ca2+]i and showed reduced levels of cytokine transcript (i.e., IL-6, IL-8, TNFalpha) and IL-6 release, suggesting that ROFA-stimulated cytokine formation was partially dependent on extracellular calcium sources. rofa 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 9882597-6 1999 BEAS-2B cells exposed to ROFA in calcium-free media failed to demonstrate increases of [Ca2+]i and showed reduced levels of cytokine transcript (i.e., IL-6, IL-8, TNFalpha) and IL-6 release, suggesting that ROFA-stimulated cytokine formation was partially dependent on extracellular calcium sources. Calcium 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 10563385-1 1999 Earlier we showed that 4-hours treatment of cells K562 with the GTP-binding protein activator AlF4- (10 mM NaF + 20 microM AlCl3) increased the DNA fragmentation on an average to 5% of the total 3H-thymidine-labeled DNA. Guanosine Triphosphate 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 10348705-2 1999 Epinephrine has been reported by several groups to suppress activation of monocytes in response to LPS, and the aim of the present study was to examine the effect of epinephrine on LPS induced IL-8 production using whole blood as a model system. Epinephrine 166-177 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 10563385-1 1999 Earlier we showed that 4-hours treatment of cells K562 with the GTP-binding protein activator AlF4- (10 mM NaF + 20 microM AlCl3) increased the DNA fragmentation on an average to 5% of the total 3H-thymidine-labeled DNA. tetrafluoroaluminate 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 10348705-3 1999 Epinephrine increased LPS induced IL-8 production in a dose-dependent manner in the whole concentration range (0.001-100 microM) and 1 microM epinephrine increased IL-8 levels with 125%. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 10563385-1 1999 Earlier we showed that 4-hours treatment of cells K562 with the GTP-binding protein activator AlF4- (10 mM NaF + 20 microM AlCl3) increased the DNA fragmentation on an average to 5% of the total 3H-thymidine-labeled DNA. Tritium 195-197 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 10563385-1 1999 Earlier we showed that 4-hours treatment of cells K562 with the GTP-binding protein activator AlF4- (10 mM NaF + 20 microM AlCl3) increased the DNA fragmentation on an average to 5% of the total 3H-thymidine-labeled DNA. Thymidine 198-207 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 10348705-3 1999 Epinephrine increased LPS induced IL-8 production in a dose-dependent manner in the whole concentration range (0.001-100 microM) and 1 microM epinephrine increased IL-8 levels with 125%. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 10348705-3 1999 Epinephrine increased LPS induced IL-8 production in a dose-dependent manner in the whole concentration range (0.001-100 microM) and 1 microM epinephrine increased IL-8 levels with 125%. Epinephrine 142-153 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 10348705-3 1999 Epinephrine increased LPS induced IL-8 production in a dose-dependent manner in the whole concentration range (0.001-100 microM) and 1 microM epinephrine increased IL-8 levels with 125%. Epinephrine 142-153 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 10348705-5 1999 The potentiating effect of epinephrine was mediated by blood platelets, since IL-8 levels in samples containing platelets and stimulated with LPS and epinephrine (1-100 microM) were significantly higher (p<0.05) than in control samples containing no platelets. Epinephrine 27-38 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 10348705-8 1999 We demonstrate for the first time that epinephrine promotes LPS induced production of IL-8 in whole blood via an effect on blood platelets. Epinephrine 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 9788508-4 1998 NiCl2 and CoCl2 upregulate, especially in concentrations of 1 mM, the expression of adhesion molecules (e.g., E-selectin and intercellular adhesion molecule-1), as well as the cytokines IL-6 and IL-8, as shown by enzyme immunoassay and Northern blot analysis. nickel chloride 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 9934491-2 1998 Truncated analogs of tripterine as cytokine (IL-1 alpha, IL-1 beta, TNF-alpha, IL-6, and IL-8) release inhibitors are discussed. celastrol 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 11498839-6 1999 In ALL, CR rate in patients with IL-8 > 100 ng/L was lower than in those with IL-8 < or = 100 ng/L (P < 0.05). Chromium 8-10 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 11498839-6 1999 In ALL, CR rate in patients with IL-8 > 100 ng/L was lower than in those with IL-8 < or = 100 ng/L (P < 0.05). Chromium 8-10 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 9788508-4 1998 NiCl2 and CoCl2 upregulate, especially in concentrations of 1 mM, the expression of adhesion molecules (e.g., E-selectin and intercellular adhesion molecule-1), as well as the cytokines IL-6 and IL-8, as shown by enzyme immunoassay and Northern blot analysis. cobaltous chloride 10-15 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 9843840-8 1998 Dexamethasone prevented IL-8 and tumor necrosis factor-alpha secretion in ventilated macrophages. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 24-60 9830008-1 1998 We previously demonstrated that tumor necrosis factor-alpha (TNFalpha) and H2O2 differentially regulate interleukin-8 (IL-8) and intercellular adhesion molecule (ICAM-1) gene expression in endothelial and epithelial cells. Hydrogen Peroxide 75-79 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 9830008-1 1998 We previously demonstrated that tumor necrosis factor-alpha (TNFalpha) and H2O2 differentially regulate interleukin-8 (IL-8) and intercellular adhesion molecule (ICAM-1) gene expression in endothelial and epithelial cells. Hydrogen Peroxide 75-79 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 9830008-2 1998 H2O2 induced IL-8 expression in the A549 and BEAS-2B epithelial cell lines, but not in the human microvessel endothelial cell line, HMEC-1 or human umbilical vein endothelial cells. Hydrogen Peroxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 9830008-10 1998 Moreover, the H2O2 concentration dependent increase in epithelial IL-8 mRNA expression directly corresponded to the H2O2 concentration dependent binding of AP-1 to the IL-8 promoter. Hydrogen Peroxide 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 9830008-10 1998 Moreover, the H2O2 concentration dependent increase in epithelial IL-8 mRNA expression directly corresponded to the H2O2 concentration dependent binding of AP-1 to the IL-8 promoter. Hydrogen Peroxide 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 9830008-10 1998 Moreover, the H2O2 concentration dependent increase in epithelial IL-8 mRNA expression directly corresponded to the H2O2 concentration dependent binding of AP-1 to the IL-8 promoter. Hydrogen Peroxide 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 9830008-10 1998 Moreover, the H2O2 concentration dependent increase in epithelial IL-8 mRNA expression directly corresponded to the H2O2 concentration dependent binding of AP-1 to the IL-8 promoter. Hydrogen Peroxide 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 9830008-14 1998 These data indicate that the cell type-specific induction of IL-8 gene expression by H2O2 and TNFalpha in HMEC-1 and A549 cells can be explained by the differential binding of AP-1 and NF-kappaB to the IL-8 promoter. Hydrogen Peroxide 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 9830008-14 1998 These data indicate that the cell type-specific induction of IL-8 gene expression by H2O2 and TNFalpha in HMEC-1 and A549 cells can be explained by the differential binding of AP-1 and NF-kappaB to the IL-8 promoter. Hydrogen Peroxide 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 9949625-11 1998 In our study, increased levels of TNF-alpha, IL-6 and especially IL-8 correlated with hepatic or renal dysfunction as evaluated by increased bilirubin and creatinine in plasma, while pulmonary complications correlated only with increased IL-6 levels. Bilirubin 141-150 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 9988429-4 1998 Histamine has been shown to increase the adhesion of leucocytes to the endothelium and to stimulate production of IL-6 and IL-8 by endothelial cells. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 9877502-10 1998 Talc-induced inflammation in patients with idiopathic spontaneous pneumothorax and malignant pleural effusion is characterized by an influx of polymorphonuclear neutrophils related to interleukin-8, followed by an accumulation of monocytes. Talc 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 184-197 9820828-4 1998 The lipid-induced stimulation of the phospholipase C/Ca2+ system was also attenuated in the dibutyryl cAMP-induced differentiated (neutrophil-like) cells, in which phospholipase C activation induced by NaF or formyl-Met-Leu-Phe was enhanced. Cyclic AMP 102-106 C-X-C motif chemokine ligand 8 Homo sapiens 202-205 9879930-3 1998 Exposure of cells to NaF for 2 h also inhibited protein synthesis, cellular ATP level and functional mitochondrial activities in a dose-dependent manner. Adenosine Triphosphate 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 9879930-4 1998 However, incubation of cells with NaF up to 12 mmol/L for 2 h depleted only 13% of cellular glutathione level. Glutathione 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 9879930-5 1998 The IC50 of NaF on cellular ATP level was about 5.75 mmol/L. Adenosine Triphosphate 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 9879930-9 1998 These results indicate that NaF can be toxic to oral mucosal fibroblasts in vitro by its inhibition of protein synthesis, mitochondrial function and depletion of cellular ATP. Adenosine Triphosphate 171-174 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 9834272-5 1998 RESULTS: Administration of the antisense oligonucleotide blocked the production of human interleukin 1beta and interleukin 8 by intestinal epithelial cells and inhibited neutrophil influx into the E. histolytica-infected intestinal xenografts. Oligonucleotides 41-56 C-X-C motif chemokine ligand 8 Homo sapiens 111-124 9949625-11 1998 In our study, increased levels of TNF-alpha, IL-6 and especially IL-8 correlated with hepatic or renal dysfunction as evaluated by increased bilirubin and creatinine in plasma, while pulmonary complications correlated only with increased IL-6 levels. Creatinine 155-165 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 9826354-0 1998 Pseudomonas pyocyanin increases interleukin-8 expression by human airway epithelial cells. Pyocyanine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 9886550-9 1998 PGE2 stimulated release of MCP-1, IL-8 and IL-10 into the maternal and of MCP-1 and IL-8 into the fetal circulation of the placenta but had no effect on RANTES release. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9886550-9 1998 PGE2 stimulated release of MCP-1, IL-8 and IL-10 into the maternal and of MCP-1 and IL-8 into the fetal circulation of the placenta but had no effect on RANTES release. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9826354-4 1998 We find that pyocyanin increases release of interleukin-8 (IL-8) by both normal and CF airway epithelial cell lines and by primary airway epithelial cells. Pyocyanine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 9918428-0 1998 Bile acids inhibit tumour necrosis factor alpha-induced interleukin-8 production in human colon epithelial cells. Bile Acids and Salts 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 9893037-3 1998 Live purified RSV (pRSV) induced a significant increase in IL-8 after 8 hr of exposure, while conditioned supernatants from pRSV-infected A549 cells (cRSV) induced IL-8 production in fresh A549 cultures within 4 hr of infection. prsv 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 9893037-4 1998 Furthermore, cRSV that had been rendered non-infectious by ultraviolet-irradiation (UV-cRSV) or ribavirin treatment also induced an increased production of IL-8 in fresh A549 cells, suggesting that RSV induced the synthesis of a soluble mediator(s) which in turn enhanced the synthesis of IL-8. crsv 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 9893037-4 1998 Furthermore, cRSV that had been rendered non-infectious by ultraviolet-irradiation (UV-cRSV) or ribavirin treatment also induced an increased production of IL-8 in fresh A549 cells, suggesting that RSV induced the synthesis of a soluble mediator(s) which in turn enhanced the synthesis of IL-8. crsv 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 289-293 9893037-4 1998 Furthermore, cRSV that had been rendered non-infectious by ultraviolet-irradiation (UV-cRSV) or ribavirin treatment also induced an increased production of IL-8 in fresh A549 cells, suggesting that RSV induced the synthesis of a soluble mediator(s) which in turn enhanced the synthesis of IL-8. crsv 87-91 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 9893037-4 1998 Furthermore, cRSV that had been rendered non-infectious by ultraviolet-irradiation (UV-cRSV) or ribavirin treatment also induced an increased production of IL-8 in fresh A549 cells, suggesting that RSV induced the synthesis of a soluble mediator(s) which in turn enhanced the synthesis of IL-8. Ribavirin 96-105 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 9893038-7 1998 Phorbol 12-myristate 13-acetate pretreatment diminished the ability of BK to stimulate IL-8 production. Tetradecanoylphorbol Acetate 0-31 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 9893038-8 1998 In addition, GF109203X, a selective protein kinase C inhibitor, blocked BK-induced IL-8 production. bisindolylmaleimide I 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 9885886-9 1998 The cAMP production elicited by NaF or forskolin was lower in septic patients than in the controls (p < 0.01). Cyclic AMP 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 9918428-8 1998 These findings suggest that bile acids inhibit TNF alpha-induced IL-8 production by the colonic cells. Bile Acids and Salts 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 9867034-1 1998 Bacteriochlorin a photodynamic therapy (BCA-PDT) caused inhibition of interleukin (IL)-8-activated neutrophil migration, at concentrations that did not induce membrane damage. bacteriochlorin a 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 70-88 9916887-1 1998 We give here evidence that Purkinje neurons (PNs) of mouse cerebellar slices studied with patch clamp technique combined with laser confocal microscopy, respond to human IL-8 and GROalpha by (i) a cytosolic Ca2+ transient compatible with inositol (1,4,5) trisphosphate (InsP3) formation; (ii) an enhancement of the neurotransmitter release; and (iii) an impairment of the long-term depression of synaptic strength (LTD). Inositol 1,4,5-Trisphosphate 238-268 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 9853284-6 1998 RESULTS: Apical stimulation of HPMC with IL-1 beta or TNF alpha resulted in a time and dose dependent up-regulation of IL-8, MCP-1 and RANTES mRNA expression and synthesis. hydroxypropylmethylcellulose-lactose matrix 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 9853284-11 1998 CONCLUSIONS: These data demonstrate that HPMC synthesize IL-8, MCP-1 and RANTES in response to inflammatory cytokines. hydroxypropylmethylcellulose-lactose matrix 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 10065903-6 1998 Cocaine also augmented apoptosis of brain endothelial cells and monocytes, increased secretion of four chemokines (interleukin-8, interferon-inducible protein-10, macrophage inflammatory protein-1alpha, and monocyte chemoattractant protein-1) and the cytokine, TNF-alpha, by human monocytes. Cocaine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 9820546-0 1998 Peroxynitrite mediates IL-8 gene expression and production in lipopolysaccharide-stimulated human whole blood. Peroxynitrous Acid 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 10022774-10 1998 Prestimulation of the G-protein activity by sodium fluoride (NaF) or cholera toxin (CT), followed by rhFSH challenge, accounted for a decrease in the cAMP-mediated responsiveness, down to 69.4 +/- 2.8 or 74.2 +/- 1.9%, of control (P < 0.001), respectively, indicating that the post-receptor events are critical for desensitization. Sodium Fluoride 44-59 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 10022774-10 1998 Prestimulation of the G-protein activity by sodium fluoride (NaF) or cholera toxin (CT), followed by rhFSH challenge, accounted for a decrease in the cAMP-mediated responsiveness, down to 69.4 +/- 2.8 or 74.2 +/- 1.9%, of control (P < 0.001), respectively, indicating that the post-receptor events are critical for desensitization. Cyclic AMP 150-154 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 10022774-15 1998 The effects of the post-receptor stimulations (NaF or CT) on [125I]iodo-rhFSH binding were minor (8-12% reduction). iodo-rhfsh 67-77 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 9820546-3 1998 The NO synthase inhibitors aminoguanidine and NG-nitro-L-arginine methyl ester (L-NAME) blocked IL-8 release by approximately 90% in response to LPS (1 microg/ml), but did not affect the production of IL-1beta or TNF-alpha. NG-Nitroarginine Methyl Ester 46-78 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 9820546-3 1998 The NO synthase inhibitors aminoguanidine and NG-nitro-L-arginine methyl ester (L-NAME) blocked IL-8 release by approximately 90% in response to LPS (1 microg/ml), but did not affect the production of IL-1beta or TNF-alpha. NG-Nitroarginine Methyl Ester 80-86 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 9820546-1 1998 Recent evidence indicates that free oxygen radicals, in particular hydroxyl radicals, may act as intracellular second messengers for the induction of IL-8, a potent chemoattractant and activator of neutrophil granulocytes. free oxygen radicals 31-51 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 9820546-4 1998 Both aminoguanidine and L-NAME blocked the induction of IL-8 mRNA by LPS. pimagedine 5-19 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 9820546-4 1998 Both aminoguanidine and L-NAME blocked the induction of IL-8 mRNA by LPS. NG-Nitroarginine Methyl Ester 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 9820546-1 1998 Recent evidence indicates that free oxygen radicals, in particular hydroxyl radicals, may act as intracellular second messengers for the induction of IL-8, a potent chemoattractant and activator of neutrophil granulocytes. Hydroxyl Radical 67-84 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 9820546-5 1998 Authentic ONOO- (2.5-80 microM) augmented IL-8 mRNA expression and stimulated IL-8 release in a concentration-dependent manner, whereas the NO-releasing compounds, S-nitroso-N-acetyl-DL-penicillamine and sodium nitroprusside failed to induce cytokine production. onoo 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9820546-2 1998 Here we report that peroxynitrite (ONOO-), formed by a reaction of nitric oxide (NO) with superoxide, mediates IL-8 gene expression and IL-8 production in LPS-stimulated human whole blood. Peroxynitrous Acid 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 9820546-5 1998 Authentic ONOO- (2.5-80 microM) augmented IL-8 mRNA expression and stimulated IL-8 release in a concentration-dependent manner, whereas the NO-releasing compounds, S-nitroso-N-acetyl-DL-penicillamine and sodium nitroprusside failed to induce cytokine production. onoo 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 9820546-6 1998 Combination of the NO-generating chemicals with a superoxide-generating system (xanthine/xanthine oxidase) markedly increased IL-8 release. Superoxides 50-60 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 9820546-2 1998 Here we report that peroxynitrite (ONOO-), formed by a reaction of nitric oxide (NO) with superoxide, mediates IL-8 gene expression and IL-8 production in LPS-stimulated human whole blood. Peroxynitrous Acid 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 9820546-8 1998 Furthermore, pyrrolidine dithiocarbamate, an inhibitor of activation of nuclear factor-gammaB, markedly attenuated the induction of IL-8 mRNA expression and IL-8 release by either LPS or ONOO-. pyrrolidine dithiocarbamic acid 13-40 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 9820546-2 1998 Here we report that peroxynitrite (ONOO-), formed by a reaction of nitric oxide (NO) with superoxide, mediates IL-8 gene expression and IL-8 production in LPS-stimulated human whole blood. oxido nitrite 35-40 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 9820546-8 1998 Furthermore, pyrrolidine dithiocarbamate, an inhibitor of activation of nuclear factor-gammaB, markedly attenuated the induction of IL-8 mRNA expression and IL-8 release by either LPS or ONOO-. pyrrolidine dithiocarbamic acid 13-40 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 9820546-8 1998 Furthermore, pyrrolidine dithiocarbamate, an inhibitor of activation of nuclear factor-gammaB, markedly attenuated the induction of IL-8 mRNA expression and IL-8 release by either LPS or ONOO-. oxido nitrite 187-192 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 9820546-2 1998 Here we report that peroxynitrite (ONOO-), formed by a reaction of nitric oxide (NO) with superoxide, mediates IL-8 gene expression and IL-8 production in LPS-stimulated human whole blood. oxido nitrite 35-40 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 9820546-8 1998 Furthermore, pyrrolidine dithiocarbamate, an inhibitor of activation of nuclear factor-gammaB, markedly attenuated the induction of IL-8 mRNA expression and IL-8 release by either LPS or ONOO-. oxido nitrite 187-192 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 9820546-9 1998 Our study identifies ONOO- as a novel signaling mechanism for IL-8 gene expression and suggests that inhibition of ONOO- formation or scavenging ONOO- may represent a novel therapeutic approach to inhibit IL-8 production that could lead to reduction of neutrophil accumulation and activation. onoo 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 9820546-2 1998 Here we report that peroxynitrite (ONOO-), formed by a reaction of nitric oxide (NO) with superoxide, mediates IL-8 gene expression and IL-8 production in LPS-stimulated human whole blood. Nitric Oxide 67-79 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 9820546-9 1998 Our study identifies ONOO- as a novel signaling mechanism for IL-8 gene expression and suggests that inhibition of ONOO- formation or scavenging ONOO- may represent a novel therapeutic approach to inhibit IL-8 production that could lead to reduction of neutrophil accumulation and activation. onoo 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 9820546-9 1998 Our study identifies ONOO- as a novel signaling mechanism for IL-8 gene expression and suggests that inhibition of ONOO- formation or scavenging ONOO- may represent a novel therapeutic approach to inhibit IL-8 production that could lead to reduction of neutrophil accumulation and activation. onoo 115-119 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 9820546-2 1998 Here we report that peroxynitrite (ONOO-), formed by a reaction of nitric oxide (NO) with superoxide, mediates IL-8 gene expression and IL-8 production in LPS-stimulated human whole blood. Nitric Oxide 67-79 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 9820546-9 1998 Our study identifies ONOO- as a novel signaling mechanism for IL-8 gene expression and suggests that inhibition of ONOO- formation or scavenging ONOO- may represent a novel therapeutic approach to inhibit IL-8 production that could lead to reduction of neutrophil accumulation and activation. onoo 115-119 C-X-C motif chemokine ligand 8 Homo sapiens 205-209 9813140-4 1998 Pretreatment with nicotine caused a significant inhibition of LPS-induced IL-1, IL-8, and PGE2 expression at the transcriptional level in U937 cells. Nicotine 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 9820546-2 1998 Here we report that peroxynitrite (ONOO-), formed by a reaction of nitric oxide (NO) with superoxide, mediates IL-8 gene expression and IL-8 production in LPS-stimulated human whole blood. Superoxides 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 9820546-2 1998 Here we report that peroxynitrite (ONOO-), formed by a reaction of nitric oxide (NO) with superoxide, mediates IL-8 gene expression and IL-8 production in LPS-stimulated human whole blood. Superoxides 90-100 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 9820546-3 1998 The NO synthase inhibitors aminoguanidine and NG-nitro-L-arginine methyl ester (L-NAME) blocked IL-8 release by approximately 90% in response to LPS (1 microg/ml), but did not affect the production of IL-1beta or TNF-alpha. pimagedine 27-41 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 9784544-9 1998 RSLA blocked H. pylori LPS-induced monocyte IL-8 release in a dose-dependent fashion (maximal inhibition 82%, P < 0.001). RSLA 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 9802986-5 1998 After treatment of HIMEC or PMEC with histamine or thrombin, a dramatic increase in supernatant IL-8 concentration was observed within 3 min, whereas no increase in IL-8 was detected in supernatants of identically treated HUVEC cultures. himec 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 9802986-5 1998 After treatment of HIMEC or PMEC with histamine or thrombin, a dramatic increase in supernatant IL-8 concentration was observed within 3 min, whereas no increase in IL-8 was detected in supernatants of identically treated HUVEC cultures. PMEC 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 9802986-5 1998 After treatment of HIMEC or PMEC with histamine or thrombin, a dramatic increase in supernatant IL-8 concentration was observed within 3 min, whereas no increase in IL-8 was detected in supernatants of identically treated HUVEC cultures. Histamine 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 9802986-6 1998 Histamine or thrombin treatment also caused IL-8-containing granules to rapidly disappear from HIMEC. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 9802986-7 1998 In HUVEC, IL-8-containing granules were inducible by treatment with recombinant human IL-1beta for 24 h; additional histamine treatment doubled IL-8 secretion from HUVEC in the same rapid manner observed for mucosal EC. Histamine 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 9802987-5 1998 IL-8 was retained in these storage organelles for several days after the removal of the stimulus and could be released by EC secretagogues such as phorbol myristate acetate, the calcium ionophore A23187, and histamine. Tetradecanoylphorbol Acetate 147-172 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9802987-5 1998 IL-8 was retained in these storage organelles for several days after the removal of the stimulus and could be released by EC secretagogues such as phorbol myristate acetate, the calcium ionophore A23187, and histamine. Calcium 178-185 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9802987-5 1998 IL-8 was retained in these storage organelles for several days after the removal of the stimulus and could be released by EC secretagogues such as phorbol myristate acetate, the calcium ionophore A23187, and histamine. Calcimycin 196-202 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9802987-5 1998 IL-8 was retained in these storage organelles for several days after the removal of the stimulus and could be released by EC secretagogues such as phorbol myristate acetate, the calcium ionophore A23187, and histamine. Histamine 208-217 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9831837-0 1998 Technetium Tc 99m hexamethyl propylene amine oxine leukocyte scintigraphy in patients with ulcerative colitis: correlation with clinical, biologic, endoscopic, and pathologic intensity, and local release of interleukin 8. technetium tc 99 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 207-220 9842932-4 1998 Despite a moderate increase of DC apoptosis in the presence of H2O2, we observed that H2O2 stimulated the production of IL-8 and TFN-alpha by DC in a dose-dependent manner. Hydrogen Peroxide 86-90 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 9858061-4 1998 THC decreased constitutive production of IL-8, MIP-1alpha, MIP-1beta, and RANTES and phorbol ester stimulated production of TNF-alpha, GM-CSF and IFN-gamma by NK cells. Dronabinol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 9784544-10 1998 RSLA also inhibited HPE-induced IL-8 release (by 93%, P < 0.001). RSLA 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 9784544-11 1998 The anti-CD14 monoclonal antibody 60bca substantially inhibited IL-8 release from HPE-stimulated monocytes (by 88%, P < 0.01), whereas the nonblocking anti-CD14 monoclonal antibody did not. 60bca 34-39 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 9732469-5 1998 The photolysis t(1/2) of phloxine B at 29 +/- 1 degreesC was 25, 32, 128, and 755 min in the buffered NaF, NaCl, NaBr, and NaI solutions, respectively. Eosine I Bluish 26-36 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 9848541-2 1998 Approximately 70% to 75% of LJP patients have impaired neutrophil chemotaxis towards a number of chemoattractants including N-formyl-methionyl-leucyl-phenyl-alanine, complement fragment C5a, leukotriene B4, and interleukin 8 (IL-8). CB 1837 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 211-224 9848541-2 1998 Approximately 70% to 75% of LJP patients have impaired neutrophil chemotaxis towards a number of chemoattractants including N-formyl-methionyl-leucyl-phenyl-alanine, complement fragment C5a, leukotriene B4, and interleukin 8 (IL-8). CB 1837 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 9848541-3 1998 The aim of the present study was to observe the role of IL-8 in the pathogenesis of LJP. CB 1837 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 9848541-9 1998 It was observed that the concentration of IL-8 demonstrated a negative correlation with gingival index in the LJP group. CB 1837 110-113 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9840646-11 1998 IL-8 generates high [Ca2+]i spikes using intracellular calcium stores only. Calcium 55-62 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9774447-2 1998 We reported previously that paclitaxel can induce interleukin (IL)-8 promoter activation in subgroups of ovarian cancer through the activation of both AP-1 and nuclear factor kappaB. Paclitaxel 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 50-68 9774447-3 1998 Further analysis of paclitaxel analogs indicates that the degree of IL-8 induction by analysis correlates with the extent of cell death; however, IL-8 itself is not the cause of cell death. Paclitaxel 20-30 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 9774447-8 1998 Paclitaxel-induced IL-8 promoter activation was inhibited by dominant-inhibitory mutants of JNK, p38, and the super-repressor form of IkappaBalpha, but not by dominant-inhibitory forms of ERK1. Paclitaxel 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 9780210-2 1998 Incubation of peripheral blood neutrophils with thapsigargin, an inhibitor of the endoplasmic reticulum Ca2+-sequestering-ATPase, causes a dose-dependent induction of IL-8 synthesis that continues for up to 8 h. Cycloheximide inhibits the thapsigargin-induced IL-8 production, suggesting the induction of protein synthesis de novo. Thapsigargin 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 9780210-2 1998 Incubation of peripheral blood neutrophils with thapsigargin, an inhibitor of the endoplasmic reticulum Ca2+-sequestering-ATPase, causes a dose-dependent induction of IL-8 synthesis that continues for up to 8 h. Cycloheximide inhibits the thapsigargin-induced IL-8 production, suggesting the induction of protein synthesis de novo. Thapsigargin 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 260-264 9780210-2 1998 Incubation of peripheral blood neutrophils with thapsigargin, an inhibitor of the endoplasmic reticulum Ca2+-sequestering-ATPase, causes a dose-dependent induction of IL-8 synthesis that continues for up to 8 h. Cycloheximide inhibits the thapsigargin-induced IL-8 production, suggesting the induction of protein synthesis de novo. Cycloheximide 212-225 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 9780210-2 1998 Incubation of peripheral blood neutrophils with thapsigargin, an inhibitor of the endoplasmic reticulum Ca2+-sequestering-ATPase, causes a dose-dependent induction of IL-8 synthesis that continues for up to 8 h. Cycloheximide inhibits the thapsigargin-induced IL-8 production, suggesting the induction of protein synthesis de novo. Thapsigargin 239-251 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 9780210-3 1998 In addition, Northern blot analysis of mRNA isolated from neutrophils indicates that thapsigargin treatment increases IL-8 mRNA in a time- and dose-dependent manner. Thapsigargin 85-97 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 9780210-5 1998 Addition of EGTA before thapsigargin inhibited the induction of IL-8 production. Egtazic Acid 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 9780210-5 1998 Addition of EGTA before thapsigargin inhibited the induction of IL-8 production. Thapsigargin 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 9780210-6 1998 Experiments in which EGTA was added at various times after thapsigargin treatment indicated that a sustained Ca2+ influx was required for maximum IL-8 production. Egtazic Acid 21-25 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 9780210-6 1998 Experiments in which EGTA was added at various times after thapsigargin treatment indicated that a sustained Ca2+ influx was required for maximum IL-8 production. Thapsigargin 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 9780210-7 1998 Ascomycin and cyclosporin A, inhibitors of the Ca2+-dependent phosphatase, calcineurin, also inhibited thapsigargin-induced IL-8 production. immunomycin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 9780210-7 1998 Ascomycin and cyclosporin A, inhibitors of the Ca2+-dependent phosphatase, calcineurin, also inhibited thapsigargin-induced IL-8 production. Cyclosporine 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 9780210-7 1998 Ascomycin and cyclosporin A, inhibitors of the Ca2+-dependent phosphatase, calcineurin, also inhibited thapsigargin-induced IL-8 production. Thapsigargin 103-115 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 9761763-5 1998 Using cultures of primary human pulmonary fibroblasts and pulmonary vascular smooth muscle cells (VSMC) we show that hypoxia (3% O2) induced transcription and translation of IL-6 (4- to 5-fold) and IL-8 (5- to 6-fold) in both cell types. Oxygen 129-131 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 9809497-1 1998 BACKGROUND: Leukotriene B4 (LTB4), a potent chemokinetic mediator for neutrophils, is enhanced by interleukin-8 (IL-8) and may play a key role in the inflammatory response of asthma. Leukotriene B4 12-26 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 9809497-1 1998 BACKGROUND: Leukotriene B4 (LTB4), a potent chemokinetic mediator for neutrophils, is enhanced by interleukin-8 (IL-8) and may play a key role in the inflammatory response of asthma. Leukotriene B4 12-26 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 9809497-2 1998 OBJECTIVE: The aim of the present study was to investigate whether zileuton, a 5-lipoxygenase antagonist known to inhibit LTB4 production and recruitment of eosinophils/neutrophils in bronchoalveolar fluid, could affect the production of LTB4 and IL-8 by allergen-stimulated peripheral blood mononuclear cells in vitro from patients with asthma and/or allergic rhinitis. zileuton 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 9809497-9 1998 CONCLUSIONS: The zileuton-induced attenuation of LTB4 production by allergen-stimulated peripheral blood mononuclear cells from patients with asthma and/or allergic rhinitis occurs independently from the allergen-stimulated IL-8 production. zileuton 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 224-228 9751519-5 1998 Basal IL-8 release by cultured hOC or hOCL was orders of magnitude greater than the release of the proinflammatory cytokines IL-1beta, IL-6, and tumor necrosis factor-alpha. (2S)-2-HYDROXYOCTANOIC ACID 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 9751519-5 1998 Basal IL-8 release by cultured hOC or hOCL was orders of magnitude greater than the release of the proinflammatory cytokines IL-1beta, IL-6, and tumor necrosis factor-alpha. Hypochlorous Acid 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 9751519-7 1998 Therefore, the potential inflammation-mediated induction of IL-8 was directly assessed using cultured hOCL. Hypochlorous Acid 102-106 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9751519-10 1998 We conclude that hOC and hOCL synthesize and secrete high constitutive and inflammation-stimulated levels of the chemokine IL-8. (2S)-2-HYDROXYOCTANOIC ACID 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 9751519-10 1998 We conclude that hOC and hOCL synthesize and secrete high constitutive and inflammation-stimulated levels of the chemokine IL-8. Hypochlorous Acid 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 9792213-7 1998 In fact, treatments of animals with (1) histamine H1 or serotonin antagonists or with (2) the mast cell stabilizer cromolyn or with (3) prior depletion of intact mast cells are maneuvers that successfully reduce eosinophil, neutrophil and monocyte extravasation in response to eotaxin, interleukin-8 or monocyte chemoattractant protein-1, respectively. histamine h1 40-52 C-X-C motif chemokine ligand 8 Homo sapiens 286-299 9820635-3 1998 Serum levels of IL-8 were also markedly increased in the patients compared to controls, and they were correlated positively with the levels of serum sE-selectin, sICAM, sVCAM, IL-1beta and TNF-alpha, and inversely with the number of circulating neutrophils. se-selectin 149-160 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 9761780-7 1998 Induction of the stress response with PGA1 and concomitant induction of I-kappaBalpha were associated with inhibition of TNF-alpha-mediated secretion of interleukin 8 and with inhibition of TNF-alpha-mediated nuclear translocation and activation of NF-kappaB. prostaglandin A1 38-42 C-X-C motif chemokine ligand 8 Homo sapiens 153-166 9792213-7 1998 In fact, treatments of animals with (1) histamine H1 or serotonin antagonists or with (2) the mast cell stabilizer cromolyn or with (3) prior depletion of intact mast cells are maneuvers that successfully reduce eosinophil, neutrophil and monocyte extravasation in response to eotaxin, interleukin-8 or monocyte chemoattractant protein-1, respectively. Cromolyn Sodium 115-123 C-X-C motif chemokine ligand 8 Homo sapiens 286-299 9831326-8 1998 Eosinophil O2- production, LTC4 release, and IL-8 production were also inhibited by sulochrin. sulochrin 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 9768679-6 1998 A 48-h treatment of cytotrophoblasts with 100 nmol/L DEX significantly reduced the production of IL-8 to 24+/-1% of control levels (P < 0.01). Dexamethasone 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 9768679-7 1998 DEX and cortisol mediated a dose-dependent inhibition of IL-8 expression, with ED50 values of 5 and 50 nmol/L, respectively. Dexamethasone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9768679-7 1998 DEX and cortisol mediated a dose-dependent inhibition of IL-8 expression, with ED50 values of 5 and 50 nmol/L, respectively. Hydrocortisone 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9759900-0 1998 Prostaglandin E2 stimulates IL-8 gene expression in human colonic epithelial cells by a posttranscriptional mechanism. Dinoprostone 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 9759900-3 1998 As PGE2 is central in gut inflammation and modulates a variety of mucosal epithelial cell functions, we determined whether PGE2 can affect the expression of IL-8. Dinoprostone 123-127 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 9809627-0 1998 Nitric oxide-mediated modulation of interleukin-8 production by a human glioblastoma cell line, T98G, cocultured with myeloid and monocytic cell lines. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 36-49 9759900-4 1998 Exogenous PGE2 induced the accumulation of IL-8 mRNA and protein production in a dose- and time-dependent manner in T84 human colonic epithelial cells. Dinoprostone 10-14 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 9809627-2 1998 Pretreatment of HL-60 or THP-1 cells with phorbol myristate acetate (PMA) enhanced their capacity to induce IL-8 production by T98G cells. Tetradecanoylphorbol Acetate 42-67 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 9809627-2 1998 Pretreatment of HL-60 or THP-1 cells with phorbol myristate acetate (PMA) enhanced their capacity to induce IL-8 production by T98G cells. Tetradecanoylphorbol Acetate 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 9809627-6 1998 Because RAW cells produce large amounts of nitric oxide (NO), we assumed that the suppression of IL-8 production was ascribable to the NO produced by the RAW cells. Nitric Oxide 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 9809627-8 1998 The involvement of NO in the suppression of IL-8 production was confirmed by the finding that N-monomethyl-L-arginine (NMMA), which inhibits NO production, reversed this suppression, whereas S-nitroso-N-acetyl-D,L-penicillamine (SNAP), a strong NO generator, suppressed IL-8 production. omega-N-Methylarginine 94-117 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 9809627-8 1998 The involvement of NO in the suppression of IL-8 production was confirmed by the finding that N-monomethyl-L-arginine (NMMA), which inhibits NO production, reversed this suppression, whereas S-nitroso-N-acetyl-D,L-penicillamine (SNAP), a strong NO generator, suppressed IL-8 production. omega-N-Methylarginine 94-117 C-X-C motif chemokine ligand 8 Homo sapiens 270-274 9792581-10 1998 Multiple regression analyses showed that arterial PCO2 was significantly correlated with SOT, LECT, and CI (r=0.51; r2=0.26; p<0.000001); the correlation became stronger considering only CSR patients (r=0.64; r2=0.4; p<0.001). pco2 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 9809627-8 1998 The involvement of NO in the suppression of IL-8 production was confirmed by the finding that N-monomethyl-L-arginine (NMMA), which inhibits NO production, reversed this suppression, whereas S-nitroso-N-acetyl-D,L-penicillamine (SNAP), a strong NO generator, suppressed IL-8 production. omega-N-Methylarginine 119-123 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 9759900-5 1998 Forskolin and dibutyryl cAMP, which increase intracellular cAMP, stimulated IL-8 in a fashion similar to that of PGE2. Colforsin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 9809627-8 1998 The involvement of NO in the suppression of IL-8 production was confirmed by the finding that N-monomethyl-L-arginine (NMMA), which inhibits NO production, reversed this suppression, whereas S-nitroso-N-acetyl-D,L-penicillamine (SNAP), a strong NO generator, suppressed IL-8 production. omega-N-Methylarginine 119-123 C-X-C motif chemokine ligand 8 Homo sapiens 270-274 9759900-5 1998 Forskolin and dibutyryl cAMP, which increase intracellular cAMP, stimulated IL-8 in a fashion similar to that of PGE2. Cyclic AMP 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 9809627-8 1998 The involvement of NO in the suppression of IL-8 production was confirmed by the finding that N-monomethyl-L-arginine (NMMA), which inhibits NO production, reversed this suppression, whereas S-nitroso-N-acetyl-D,L-penicillamine (SNAP), a strong NO generator, suppressed IL-8 production. snap 229-233 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 9759900-6 1998 PGE2 and PGE2 receptor agonists coupling through EP4 receptors elevated intracellular cAMP and up-regulated IL-8 mRNA expression by activating protein kinase A. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 9759900-8 1998 However, PGE2, forskolin, and PMA enhanced the stability of IL-8 mRNA transcripts, suggesting the involvement of posttranscriptional regulation. Dinoprostone 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9759900-8 1998 However, PGE2, forskolin, and PMA enhanced the stability of IL-8 mRNA transcripts, suggesting the involvement of posttranscriptional regulation. Colforsin 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9759900-8 1998 However, PGE2, forskolin, and PMA enhanced the stability of IL-8 mRNA transcripts, suggesting the involvement of posttranscriptional regulation. Tetradecanoylphorbol Acetate 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9759900-9 1998 Chloramphenicol acetyltransferase reporter gene transfection studies confirmed the presence of a PGE2 responsive cis-element(s) in the IL-8 3" untranslated region. Dinoprostone 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 9759900-11 1998 These results highlight a novel role for PGE2 in up-regulating IL-8 gene expression by colonic epithelial cells, which may contribute to exacerbation of inflammation in the gastrointestinal tract. Dinoprostone 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 9766632-1 1998 Interleukin-8 (IL-8) priming was studied in neutrophils to examine its dependency on altered calcium fluxes and for similarity to lipopolysaccharide (LPS). Calcium 93-100 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9766632-4 1998 In comparison to LPS and tumor necrosis factor (TNF), IL-8 was a much weaker priming agent as measured by either O2- or H2O2 production. Oxygen 113-115 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9740146-10 1998 TPA (10 nmol/L) also stimulated the production of IL-6 and IL-8 by these cells, but inhibited that of monocyte chemoattractant protein-1. Tetradecanoylphorbol Acetate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 9766632-4 1998 In comparison to LPS and tumor necrosis factor (TNF), IL-8 was a much weaker priming agent as measured by either O2- or H2O2 production. Hydrogen Peroxide 120-124 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9766632-5 1998 Despite their large disparity in potency, IL-8 and LPS printing were additive using fMLP, a receptor-dependent stimulator, and synergistic using the post-receptor, protein kinase C activator, phorbol 12-myristate 13-acetate (PMA) to trigger the respiratory burst. Tetradecanoylphorbol Acetate 192-223 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9766632-5 1998 Despite their large disparity in potency, IL-8 and LPS printing were additive using fMLP, a receptor-dependent stimulator, and synergistic using the post-receptor, protein kinase C activator, phorbol 12-myristate 13-acetate (PMA) to trigger the respiratory burst. Tetradecanoylphorbol Acetate 225-228 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9784408-4 1998 Finally, the specific MEK inhibitor PD98059 inhibited ICAM-1-induced IL-8 and RANTES production in endothelial cells. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 36-43 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 9728050-7 1998 The same acute exposure to As, V, or Zn that activated MAPK was sufficient to induce a subsequent increase in IL-8 protein expression in BEAS cells. Arsenic 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 9728050-7 1998 The same acute exposure to As, V, or Zn that activated MAPK was sufficient to induce a subsequent increase in IL-8 protein expression in BEAS cells. Vanadium 31-32 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 9728050-7 1998 The same acute exposure to As, V, or Zn that activated MAPK was sufficient to induce a subsequent increase in IL-8 protein expression in BEAS cells. Zinc 37-39 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 9730996-5 1998 There was a significant (p < 0.05) decrease in sputum leukocyte density and IL-1beta, IL-8, and LTB4 after fluticasone treatment. Fluticasone 110-121 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 9829345-6 1998 Plasma glucose level was determined in NaF preserved plasma using the glucose oxidase method. Glucose 7-14 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 10557188-7 1998 RESULTS: Part 1: IL-8 level in the PMSF samples was significantly greater than that in the control group (3.01 +/- 5.79 mg/L vs 0.05 +/- 0.15 mg/L, respectively P < .001). Phenylmethylsulfonyl Fluoride 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 9786474-6 1998 The production of both IL-8 (a potent neutrophil activator) and TNF-alpha in the human monocytic THP-1 cell line was reduced by fosfomycin-treated basolateral medium in this system. Fosfomycin 128-138 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 9831176-9 1998 Dexamethasone partially inhibited the cytokine-induced release of MCP-1 and IL-8 and the expression of ICAM-1, CD40, and HLA class II molecules by human bronchial epithelial cells. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 9758900-0 1998 Suppressive effects of SP-A on ionomycin-induced IL-8 production and release by eosinophils. Ionomycin 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 9725262-3 1998 Binding and competition studies with 125I-labeled IL-8 and its homologue melanoma growth stimulating activity (125I-labeled MGSA) revealed two specific binding sites for IL-8, K1 = 1.1 x 10(11) M(-1) and K2 = 5 x 10(7) M(-1); and for MGSA, K1 = 2.8 x 10(10) M(-1) and K2 = 5 x 10(7) M(-1). Iodine-125 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 9725250-9 1998 The nonselective COX inhibitor indomethacin and the selective COX-2 inhibitor NS-398 strongly inhibited BK-stimulated PGE2 and IL-8 production. Indomethacin 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 9725250-10 1998 The COX substrate arachidonic acid also caused PGE2 and IL-8 production, and its effect was inhibited by nonselective COX inhibitors but unaffected by NS-398. Arachidonic Acid 18-34 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 9725250-11 1998 Both the BK- and arachidonic acid-induced IL-8 production was inhibited by the protein synthesis inhibitors cycloheximide and actinomycin D and by the steroid dexamethasone. Arachidonic Acid 17-33 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9725250-9 1998 The nonselective COX inhibitor indomethacin and the selective COX-2 inhibitor NS-398 strongly inhibited BK-stimulated PGE2 and IL-8 production. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 78-84 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 9725250-11 1998 Both the BK- and arachidonic acid-induced IL-8 production was inhibited by the protein synthesis inhibitors cycloheximide and actinomycin D and by the steroid dexamethasone. Cycloheximide 108-121 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9725262-3 1998 Binding and competition studies with 125I-labeled IL-8 and its homologue melanoma growth stimulating activity (125I-labeled MGSA) revealed two specific binding sites for IL-8, K1 = 1.1 x 10(11) M(-1) and K2 = 5 x 10(7) M(-1); and for MGSA, K1 = 2.8 x 10(10) M(-1) and K2 = 5 x 10(7) M(-1). Iodine-125 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 9725250-11 1998 Both the BK- and arachidonic acid-induced IL-8 production was inhibited by the protein synthesis inhibitors cycloheximide and actinomycin D and by the steroid dexamethasone. Dactinomycin 126-139 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9725250-11 1998 Both the BK- and arachidonic acid-induced IL-8 production was inhibited by the protein synthesis inhibitors cycloheximide and actinomycin D and by the steroid dexamethasone. Steroids 151-158 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9725250-11 1998 Both the BK- and arachidonic acid-induced IL-8 production was inhibited by the protein synthesis inhibitors cycloheximide and actinomycin D and by the steroid dexamethasone. Dexamethasone 159-172 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9725262-3 1998 Binding and competition studies with 125I-labeled IL-8 and its homologue melanoma growth stimulating activity (125I-labeled MGSA) revealed two specific binding sites for IL-8, K1 = 1.1 x 10(11) M(-1) and K2 = 5 x 10(7) M(-1); and for MGSA, K1 = 2.8 x 10(10) M(-1) and K2 = 5 x 10(7) M(-1). Iodine-125 111-115 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 9725250-12 1998 Furthermore, exogenous PGE2 and calcium ionophore A23187 also stimulated IL-8 release. Dinoprostone 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 9725250-12 1998 Furthermore, exogenous PGE2 and calcium ionophore A23187 also stimulated IL-8 release. Calcium 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 9725262-3 1998 Binding and competition studies with 125I-labeled IL-8 and its homologue melanoma growth stimulating activity (125I-labeled MGSA) revealed two specific binding sites for IL-8, K1 = 1.1 x 10(11) M(-1) and K2 = 5 x 10(7) M(-1); and for MGSA, K1 = 2.8 x 10(10) M(-1) and K2 = 5 x 10(7) M(-1). Iodine-125 111-115 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 9725250-12 1998 Furthermore, exogenous PGE2 and calcium ionophore A23187 also stimulated IL-8 release. Calcimycin 50-56 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 9759922-12 1998 Consistent with this observation is that treatments either with KA and NMDA induced an inhibition (about 30%) of NaF-stimulated PI hydrolysis which occurs through the direct activation of G proteins. N-Methylaspartate 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 9725250-13 1998 BK-induced IL-8 release was mimicked by the BK B2 receptor agonist (Tyr(Me)8)-BK and was potently inhibited by the selective B2 receptor antagonist HOE-140. tyr(me)8 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 9725250-13 1998 BK-induced IL-8 release was mimicked by the BK B2 receptor agonist (Tyr(Me)8)-BK and was potently inhibited by the selective B2 receptor antagonist HOE-140. 4-hydroxy-2-octenal 148-151 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 9725250-14 1998 These results suggest that human ASM can be a source of IL-8 and also that endogenous prostanoids, involving both COX-1 and COX-2, have a novel role in mediating BK-induced IL-8 production. Prostaglandins 86-97 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 10921031-8 1998 CONCLUSION: Serum levels of IL-6, sgp130, IL-8 may reflect patient"s responsiveness to ATRA treatment, predict hyperleukocytosis and intercurrent infection. Tretinoin 87-91 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9745529-0 1998 Anti-rat IL-8 (CINC) monoclonal antibody administration reduces ischemia-reperfusion injury in small intestine. Zinc 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 9744647-3 1998 After incubating 24 h, the combination of lipopolysaccharide and Fragmin induced significantly greater concentrations of interleukin 1 (IL)-1beta (25+/-10 ng/mL; x +/- standard error), IL-8 (21+/-6), and tumor necrosis factor (TNF)alpha (.48+/-.24) compared with heparinized blood (p < .05). Dalteparin 65-72 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 9744647-5 1998 Average levels of proinflammatory cytokines (IL-1beta, IL-6, IL-8, and TNFalpha) were greater with Fragmin anticoagulation for 36 of 40 comparisons, and patterns were similar for 6 h and 24 h incubations. Dalteparin 99-106 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 9708989-2 1998 Using flow cytometric assays and pertussis toxin (PT) treatment of human neutrophils, we have shown that actin polymerization stimulated with the chemoattractants N-formyl-Met-Leu-Phe, leukotriene B4, and interleukin-8 exhibits threshold behavior in terms of G-protein number. Leukotrienes 185-196 C-X-C motif chemokine ligand 8 Homo sapiens 205-218 9685620-0 1998 The effect of interleukin-8 and granulocyte macrophage colony stimulating factor on the response of neutrophils to formyl methionyl leucyl phenylalanine. N-Formylmethionine Leucyl-Phenylalanine 115-152 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 9712064-4 1998 Expression of ICAM-1, VCAM-1, and E-selectin was not altered following incubation with tryptase, but the potent granulocyte chemoattractant IL-8 was released in a dose-dependent fashion in response to physiologically relevant concentrations, with maximal levels in supernatants after 24 h. The actions of tryptase on HUVEC were inhibited by heat inactivation of the enzyme, or by preincubating with the protease inhibitors leupeptin or benzamidine, suggesting a requirement for an intact catalytic site. leupeptin 423-432 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 9712064-4 1998 Expression of ICAM-1, VCAM-1, and E-selectin was not altered following incubation with tryptase, but the potent granulocyte chemoattractant IL-8 was released in a dose-dependent fashion in response to physiologically relevant concentrations, with maximal levels in supernatants after 24 h. The actions of tryptase on HUVEC were inhibited by heat inactivation of the enzyme, or by preincubating with the protease inhibitors leupeptin or benzamidine, suggesting a requirement for an intact catalytic site. benzamidine 436-447 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 9738952-6 1998 On the other hand, tetrodotoxin (TTX) and cyclosporin A inhibited only the NaF-induced 45Ca2+ influx (IC50 = 21 mol/l and 28 mol/l, respectively). Tetrodotoxin 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 9698365-2 1998 The binding site on the chemokine interleukin-8 (IL-8) for the glycosaminoglycan heparin has been characterized using a systematic series of site-directed mutants of IL-8 in which the basic residues of the protein have been replaced by alanine. Alanine 236-243 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 9698365-2 1998 The binding site on the chemokine interleukin-8 (IL-8) for the glycosaminoglycan heparin has been characterized using a systematic series of site-directed mutants of IL-8 in which the basic residues of the protein have been replaced by alanine. Alanine 236-243 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 9698365-4 1998 Heparin-derived disaccharides that could disrupt the IL-8-heparin Sepharose interaction were identified by a competitive binding assay. heparin-derived disaccharides 0-29 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9698365-4 1998 Heparin-derived disaccharides that could disrupt the IL-8-heparin Sepharose interaction were identified by a competitive binding assay. Sepharose 66-75 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9698365-5 1998 Heteronuclear NMR spectroscopic titration of 15N-labeled IL-8 with a trisulfated disaccharide revealed a cluster of residues on IL-8 which were perturbed by disaccharide binding. 15n 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9698365-5 1998 Heteronuclear NMR spectroscopic titration of 15N-labeled IL-8 with a trisulfated disaccharide revealed a cluster of residues on IL-8 which were perturbed by disaccharide binding. 15n 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 9698365-5 1998 Heteronuclear NMR spectroscopic titration of 15N-labeled IL-8 with a trisulfated disaccharide revealed a cluster of residues on IL-8 which were perturbed by disaccharide binding. trisulfated disaccharide 69-93 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9698365-5 1998 Heteronuclear NMR spectroscopic titration of 15N-labeled IL-8 with a trisulfated disaccharide revealed a cluster of residues on IL-8 which were perturbed by disaccharide binding. trisulfated disaccharide 69-93 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 9698365-5 1998 Heteronuclear NMR spectroscopic titration of 15N-labeled IL-8 with a trisulfated disaccharide revealed a cluster of residues on IL-8 which were perturbed by disaccharide binding. Disaccharides 81-93 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9738952-6 1998 On the other hand, tetrodotoxin (TTX) and cyclosporin A inhibited only the NaF-induced 45Ca2+ influx (IC50 = 21 mol/l and 28 mol/l, respectively). Tetrodotoxin 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 9698365-5 1998 Heteronuclear NMR spectroscopic titration of 15N-labeled IL-8 with a trisulfated disaccharide revealed a cluster of residues on IL-8 which were perturbed by disaccharide binding. Disaccharides 81-93 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 9698365-6 1998 These data identify a heparin-binding surface on IL-8 that includes the C-terminal alpha-helix and the proximal loop around residues 18-23. Heparin 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 9738952-6 1998 On the other hand, tetrodotoxin (TTX) and cyclosporin A inhibited only the NaF-induced 45Ca2+ influx (IC50 = 21 mol/l and 28 mol/l, respectively). Cyclosporine 42-55 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 9738952-9 1998 Thus, the Gardos effect induced by NaVO3 and NaF represents two phenomena activated by different mechanisms present in the cryptic state in the RBC membrane. gardos 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 9700090-4 1998 ICI 200,355 (an inhibitor of neutrophil elastase and proteinase-3) or secretory leukocyte protease inhibitor (an inhibitor of elastase but not of proteinase-3) abolished IL-8-induced GC degranulation, implicating elastase. ici 200, 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 9665313-0 1998 Stimulation of monocyte interleukin-8 by lipid peroxidation products: a mechanism for alcohol-induced liver injury. Alcohols 86-93 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 9665313-3 1998 Peroxidized fatty acids (arachidonic and linolenic) as well as microsomal membranes stimulated IL-8 production by peripheral blood monocytes whereas ethanol and acetaldehyde did not. Fatty Acids 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 9665313-4 1998 Hydrocortisone (5 microg/ml) prevented the IL-8 stimulation by peroxidized fatty acids. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 9665313-4 1998 Hydrocortisone (5 microg/ml) prevented the IL-8 stimulation by peroxidized fatty acids. Fatty Acids 75-86 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 9705848-5 1998 The specific p38 MAP kinase inhibitor SB 203580 inhibited cooling and rewarming-induced IL-8 expression, indicating that cooling and rewarming-induced IL-8 expression in BEC was mediated through p38 MAP kinase-dependent pathway. SB 203580 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 9705848-5 1998 The specific p38 MAP kinase inhibitor SB 203580 inhibited cooling and rewarming-induced IL-8 expression, indicating that cooling and rewarming-induced IL-8 expression in BEC was mediated through p38 MAP kinase-dependent pathway. SB 203580 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 9665313-5 1998 Ethanol-induced lipid peroxidation may secondarily further alcohol-induced liver injury through IL-8 chemotaxis of neutrophils. Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 9698598-0 1998 Inhibition of TNF-alpha-induced NF-kappaB activation and IL-8 release in A549 cells with the proteasome inhibitor MG-132. benzyloxycarbonylleucyl-leucyl-leucine aldehyde 114-120 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9665313-5 1998 Ethanol-induced lipid peroxidation may secondarily further alcohol-induced liver injury through IL-8 chemotaxis of neutrophils. Alcohols 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 9727645-6 1998 Both prednisone and a prostaglandin analog were effective in downregulating TNF and interleukin-8 production. Prednisone 5-15 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 9727645-6 1998 Both prednisone and a prostaglandin analog were effective in downregulating TNF and interleukin-8 production. Prostaglandins 22-35 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 9698598-4 1998 However, pretreatment of the cells with the proteasome inhibitor N-cbz-Leu-Leu-leucinal (MG-132, 10 microM) reversed the effects of TNF-alpha on IL-8 release from A549 cells (as determined with an enzyme-linked immunosorbent assay [ELISA]) and on IL-8 gene transcription (as determined with reporter-gene assays). n-cbz 65-70 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 9698598-4 1998 However, pretreatment of the cells with the proteasome inhibitor N-cbz-Leu-Leu-leucinal (MG-132, 10 microM) reversed the effects of TNF-alpha on IL-8 release from A549 cells (as determined with an enzyme-linked immunosorbent assay [ELISA]) and on IL-8 gene transcription (as determined with reporter-gene assays). n-cbz 65-70 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 9698598-4 1998 However, pretreatment of the cells with the proteasome inhibitor N-cbz-Leu-Leu-leucinal (MG-132, 10 microM) reversed the effects of TNF-alpha on IL-8 release from A549 cells (as determined with an enzyme-linked immunosorbent assay [ELISA]) and on IL-8 gene transcription (as determined with reporter-gene assays). Leucine 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 9698598-4 1998 However, pretreatment of the cells with the proteasome inhibitor N-cbz-Leu-Leu-leucinal (MG-132, 10 microM) reversed the effects of TNF-alpha on IL-8 release from A549 cells (as determined with an enzyme-linked immunosorbent assay [ELISA]) and on IL-8 gene transcription (as determined with reporter-gene assays). Leucine 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 9756185-3 1998 Further to these observations we report on the inhibition by theophylline of NF-kappaB, a key transcription factor found in human purified mast cells, which plays a role in the transcription of TNF alpha, GM-CSF, and IL-8 within this cell. Theophylline 61-73 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 9723955-0 1998 Regulation of RANTES and IL-8 production in normal human dermal fibroblasts by active vitamin D3 (tacalcitol). Cholecalciferol 86-96 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 9723955-0 1998 Regulation of RANTES and IL-8 production in normal human dermal fibroblasts by active vitamin D3 (tacalcitol). 1 alpha,24-dihydroxyvitamin D3 98-108 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 9723955-6 1998 Tacalcitol suppressed RANTES and IL-8 production dose-dependently at concentrations between 10(-12) M and 10(-7) M. 3. 1 alpha,24-dihydroxyvitamin D3 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 9723955-8 1998 Tacalcitol decreased IL-8 production dose-dependently as observed in the TNF-alpha-treated cells. 1 alpha,24-dihydroxyvitamin D3 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 9723955-11 1998 Three active vitamin D3 compounds, tacalcitol, 1alpha,25-dihydroxyvitamin D3 and MC903 (calcipotriol), inhibited the production of RANTES and IL-8, with very similar potencies. Cholecalciferol 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 9723955-11 1998 Three active vitamin D3 compounds, tacalcitol, 1alpha,25-dihydroxyvitamin D3 and MC903 (calcipotriol), inhibited the production of RANTES and IL-8, with very similar potencies. 1 alpha,24-dihydroxyvitamin D3 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 9723955-11 1998 Three active vitamin D3 compounds, tacalcitol, 1alpha,25-dihydroxyvitamin D3 and MC903 (calcipotriol), inhibited the production of RANTES and IL-8, with very similar potencies. Calcitriol 47-76 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 9723955-11 1998 Three active vitamin D3 compounds, tacalcitol, 1alpha,25-dihydroxyvitamin D3 and MC903 (calcipotriol), inhibited the production of RANTES and IL-8, with very similar potencies. calcipotriene 81-86 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 9723955-11 1998 Three active vitamin D3 compounds, tacalcitol, 1alpha,25-dihydroxyvitamin D3 and MC903 (calcipotriol), inhibited the production of RANTES and IL-8, with very similar potencies. calcipotriene 88-100 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 9723955-13 1998 Cyclosporin A significantly stimulated RANTES production at 10(-6) M and IL-8 production at 10(-7) M and 10(-6) M. 5. Cyclosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 9756186-4 1998 In this study we investigated the ability of theophylline to inhibit the release of preformed GM-CSF and IL-8 from eosinophils in vitro, as these cytokines may serve an autocrine function in eosinophil survival in vivo. Theophylline 45-57 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 9723671-0 1998 Diisocyanate antigen-enhanced production of monocyte chemoattractant protein-1, IL-8, and tumor necrosis factor-alpha by peripheral mononuclear cells of workers with occupational asthma. 4,4'-diphenylmethane diisocyanate 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 80-117 9710230-4 1998 TIL matrix invasion elicited by TC is inhibited by the addition of neutralizing antisera specific for IL-8 and MCP-1, demonstrating the direct relationship between chemokine release by TC and TIL invasion. Technetium 32-34 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 9710230-4 1998 TIL matrix invasion elicited by TC is inhibited by the addition of neutralizing antisera specific for IL-8 and MCP-1, demonstrating the direct relationship between chemokine release by TC and TIL invasion. Technetium 185-187 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 9719033-6 1998 The IL-8 mRNA accumulation in response to P. intermedia LPS was inhibited by tosylphenyl-alanyl chloromethyl-ketone, an inhibitor of NF-kappaB activation, although the NF-kappaB activation itself was not altered by IFN-gamma. Tosylphenylalanyl Chloromethyl Ketone 77-115 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 9726445-5 1998 Using human Hep G2 cells, it was demonstrated that, in contrast to lipopolysaccharides (LPS), both tumor necrosis factor-alpha (TNF-beta) and H2O2 are potent inducers of IL-8, presumably acting via protein kinase C (PKC)-dependent pathways. Hydrogen Peroxide 142-146 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 9712106-9 1998 Inhibition of NO synthesis with the competitive inhibitor NG-monomethyl-L-arginine (L-NMMA) led to enhancement of IL-6, IL-8, and PGE2 production stimulated by either IL-1beta alone or in combination with LPS, whereas the inhibition of proteoglycan production by IL-1beta was not modified by L-NMMA. omega-N-Methylarginine 58-82 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 9726445-7 1998 Both IL-8 and MIP-2 secretion were inhibited, although to varying degrees, by such antioxidants as TMTU, DMSO, catalase, and N-acetylcysteine. tetramethylthiourea 99-103 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 9726445-7 1998 Both IL-8 and MIP-2 secretion were inhibited, although to varying degrees, by such antioxidants as TMTU, DMSO, catalase, and N-acetylcysteine. Dimethyl Sulfoxide 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 9726445-7 1998 Both IL-8 and MIP-2 secretion were inhibited, although to varying degrees, by such antioxidants as TMTU, DMSO, catalase, and N-acetylcysteine. Acetylcysteine 125-141 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 9726445-8 1998 Furthermore, in vitro TNF-alpha neutralization experiments and transfection of Hep G2 cells with an IL-8 construct confirmed that TNF-alpha and H2O2 directly stimulate IL-8 secretion. Hydrogen Peroxide 144-148 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 9726445-8 1998 Furthermore, in vitro TNF-alpha neutralization experiments and transfection of Hep G2 cells with an IL-8 construct confirmed that TNF-alpha and H2O2 directly stimulate IL-8 secretion. Hydrogen Peroxide 144-148 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 9712106-0 1998 Nitric oxide downregulates interleukin 1beta (IL-1beta) stimulated IL-6, IL-8, and prostaglandin E2 production by human chondrocytes. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 9712106-9 1998 Inhibition of NO synthesis with the competitive inhibitor NG-monomethyl-L-arginine (L-NMMA) led to enhancement of IL-6, IL-8, and PGE2 production stimulated by either IL-1beta alone or in combination with LPS, whereas the inhibition of proteoglycan production by IL-1beta was not modified by L-NMMA. omega-N-Methylarginine 84-90 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 9687567-8 1998 Of the mRNAs tested, only those encoding monocyte chemotactic protein-1 (approximately 2-fold over basal) and interleukin-8 (approximately 6-fold over basal) are induced by histamine; both of these responses are suppressed by CsA and FK506. Histamine 173-182 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 9690225-9 1998 RESULTS: Compared to the control group, PBMC from uremic patients on conservative therapy and treated by CU showed a clear reduction in the cytokine release, while PMMA and PA membranes were able to normalize IL-6, IL-8 and MCP-1 protein concentration, which had been reduced by CU treatment. Nylons 173-175 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 9690225-9 1998 RESULTS: Compared to the control group, PBMC from uremic patients on conservative therapy and treated by CU showed a clear reduction in the cytokine release, while PMMA and PA membranes were able to normalize IL-6, IL-8 and MCP-1 protein concentration, which had been reduced by CU treatment. cuprammonium cellulose 105-107 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 9690225-9 1998 RESULTS: Compared to the control group, PBMC from uremic patients on conservative therapy and treated by CU showed a clear reduction in the cytokine release, while PMMA and PA membranes were able to normalize IL-6, IL-8 and MCP-1 protein concentration, which had been reduced by CU treatment. Polymethyl Methacrylate 164-168 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 9687567-8 1998 Of the mRNAs tested, only those encoding monocyte chemotactic protein-1 (approximately 2-fold over basal) and interleukin-8 (approximately 6-fold over basal) are induced by histamine; both of these responses are suppressed by CsA and FK506. Cyclosporine 226-229 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 9687567-8 1998 Of the mRNAs tested, only those encoding monocyte chemotactic protein-1 (approximately 2-fold over basal) and interleukin-8 (approximately 6-fold over basal) are induced by histamine; both of these responses are suppressed by CsA and FK506. Tacrolimus 234-239 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 9704773-4 1998 Correlations were found between hyaluronic acid concentrations and interleukin-1beta (P = .018) and interleukin-8 (P = .003) concentrations in cervical mucus. Hyaluronic Acid 32-47 C-X-C motif chemokine ligand 8 Homo sapiens 100-113 9828857-12 1998 IL-8+ cells were less prominent in steroid treated patients than in patients not receiving treatment (30 cells/mm2 versus 60 cells/mm2, p < 0.05). Steroids 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9670044-4 1998 Met-enkephalin, as well as morphine, inhibited IL-8-induced chemotaxis of human neutrophils and macrophage inflammatory protein (MIP)-1alpha, regulated upon activation, normal T expressed and secreted (RANTES), and monocyte chemoattractant protein 1, but not MIP-1beta-induced chemotaxis of human monocytes. Morphine 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9707512-6 1998 IL-8 and MIP-2 secretion induced either by the metals or H2O2 were inhibited by antioxidants such as tetramethyl-thiourea and N-acetyl-cysteine. Hydrogen Peroxide 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9707512-6 1998 IL-8 and MIP-2 secretion induced either by the metals or H2O2 were inhibited by antioxidants such as tetramethyl-thiourea and N-acetyl-cysteine. tetramethylthiourea 101-121 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9707512-6 1998 IL-8 and MIP-2 secretion induced either by the metals or H2O2 were inhibited by antioxidants such as tetramethyl-thiourea and N-acetyl-cysteine. Acetylcysteine 126-143 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9655727-14 1998 These data suggest that exposure to fuel-oil ash results in acute upper airway inflammation, potentially mediated by increased IL-8 levels and the recruitment and activation of polymorphonuclear leukocytes. Oils 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 9704773-5 1998 Cytokines (especially interleukin-8) stimulated hyaluronic acid production by cultured cervical fibroblasts. Hyaluronic Acid 48-63 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 9704790-8 1998 In placentas delivered spontaneously, onapristone significantly increased production of interleukin 8 (P < .05), whereas in those from cesarean deliveries lilopristone caused a significant increase in production (P < .05). onapristone 38-49 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 9692902-6 1998 GCP-2 desensitized the calcium increase induced by IL-8 in both CXCR1-transfected and CXCR2-transfected cells, but ENA-78 only affected the IL-8-induced calcium response in CXCR2-transfectants. Calcium 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 9698090-2 1998 Previously, we showed that the protein kinase inhibitor staurosporine potentiates IL-1-stimulated IL-8 production in human keratinocytes. Staurosporine 56-69 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 9698090-3 1998 Moreover, recent studies by other investigators demonstrated that staurosporine treatment alone results in a concentration-dependent increase in IL-8 mRNA and protein production. Staurosporine 66-79 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 9698090-6 1998 The ability of staurosporine to activate NF-kappaB was investigated further, using luciferase reporters under the control of the HIV-LTR or IL-8 core promoter transfected into human U937 cells. Staurosporine 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 9692902-6 1998 GCP-2 desensitized the calcium increase induced by IL-8 in both CXCR1-transfected and CXCR2-transfected cells, but ENA-78 only affected the IL-8-induced calcium response in CXCR2-transfectants. Calcium 153-160 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 9738983-9 1998 Intracellular H2O2 production and IL-8 release were transiently induced immediately after treatment with platinum compounds, leading to IL-1 release when H2O2 production was eliminated. Platinum 105-113 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9665286-9 1998 Go6976, which inhibits certain isoforms of PKC, inhibited production of both IL-8 and TNF-alpha. Go 6976 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 9722036-0 1998 Effect of L-NAME, an inhibitor of nitric oxide synthesis, on plasma levels of IL-6, IL-8, TNF alpha and nitrite/nitrate in human septic shock. NG-Nitroarginine Methyl Ester 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9749865-6 1998 Hydrocortisone significantly suppressed the production of IL-6, IL-8, and GM-CSF by TCCs from AH of VKH patients. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 9749865-7 1998 Tacrolimus also significantly suppressed the production of IL-8 and GM-CSF by the TCCs. Tacrolimus 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 9738983-9 1998 Intracellular H2O2 production and IL-8 release were transiently induced immediately after treatment with platinum compounds, leading to IL-1 release when H2O2 production was eliminated. Hydrogen Peroxide 154-158 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9624135-0 1998 Defining the interleukin-8-binding domain of heparan sulfate. Heparitin Sulfate 45-60 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 10070569-4 1998 Results showed that a 48 h O2 exposure was associated with two distinct patterns of response: a decrease in TNF-alpha, IL-1 beta and IL-6 expression, and an increase in IL-8. Oxygen 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 10070569-6 1998 We confirmed that a 48 h O2 exposure led to similar changes with a decrease in TNF-alpha, IL-1 beta and IL-6 production and an increase in IL-8. Oxygen 25-27 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 11189515-0 1998 [Expression of interleukin-8 and its receptor in acute promyelocytic leukemia under all-trans retinoic acid treatment]. Tretinoin 94-107 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 11189515-1 1998 OBJECTIVE: To evaluate the clinical significance of expression of interleukin-(IL-8) and its type A receptor(IL-8RA) in acute promyelocytic leukemia(APL) patients under all trans-retinoic acid(ATRA) induction. Tretinoin 173-192 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 11189515-1 1998 OBJECTIVE: To evaluate the clinical significance of expression of interleukin-(IL-8) and its type A receptor(IL-8RA) in acute promyelocytic leukemia(APL) patients under all trans-retinoic acid(ATRA) induction. Tretinoin 193-197 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 11189515-9 1998 CONCLUSION: ATRA inhibited IL-8 secretion of APL cells while increased the expression of IL-8RA. Tretinoin 12-16 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9624135-1 1998 Interleukin-8, a member of the CXC chemokine family, has been shown to bind to glycosaminoglycans. Glycosaminoglycans 79-97 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9624135-3 1998 By using selectively modified heparin and heparan sulfate fragments in a nitrocellulose filter trapping system, we have analyzed sequence requirements for interleukin-8 binding to heparin/heparan sulfate. Heparin 180-187 C-X-C motif chemokine ligand 8 Homo sapiens 155-168 9624135-3 1998 By using selectively modified heparin and heparan sulfate fragments in a nitrocellulose filter trapping system, we have analyzed sequence requirements for interleukin-8 binding to heparin/heparan sulfate. Heparitin Sulfate 188-203 C-X-C motif chemokine ligand 8 Homo sapiens 155-168 9624135-4 1998 We demonstrate that the affinity of a monomeric interleukin-8 molecule for heparin/heparan sulfate is too weak to allow binding at physiological ionic strength, whereas the dimeric form of the protein mediates binding to two sulfated domains of heparan sulfate. Heparin 75-82 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 9624135-4 1998 We demonstrate that the affinity of a monomeric interleukin-8 molecule for heparin/heparan sulfate is too weak to allow binding at physiological ionic strength, whereas the dimeric form of the protein mediates binding to two sulfated domains of heparan sulfate. Heparitin Sulfate 83-98 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 9624135-4 1998 We demonstrate that the affinity of a monomeric interleukin-8 molecule for heparin/heparan sulfate is too weak to allow binding at physiological ionic strength, whereas the dimeric form of the protein mediates binding to two sulfated domains of heparan sulfate. Heparitin Sulfate 245-260 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 9624135-6 1998 Binding to interleukin-8 correlates with the occurrence of the di-O-sulfated disaccharide unit -IdceA(2-OSO3)-GlcNSO3(6-OSO3)-. di-o-sulfated disaccharide 63-89 C-X-C motif chemokine ligand 8 Homo sapiens 11-24 9624135-6 1998 Binding to interleukin-8 correlates with the occurrence of the di-O-sulfated disaccharide unit -IdceA(2-OSO3)-GlcNSO3(6-OSO3)-. 2-oso3 102-108 C-X-C motif chemokine ligand 8 Homo sapiens 11-24 9624135-6 1998 Binding to interleukin-8 correlates with the occurrence of the di-O-sulfated disaccharide unit -IdceA(2-OSO3)-GlcNSO3(6-OSO3)-. glcnso3 110-117 C-X-C motif chemokine ligand 8 Homo sapiens 11-24 9624135-6 1998 Binding to interleukin-8 correlates with the occurrence of the di-O-sulfated disaccharide unit -IdceA(2-OSO3)-GlcNSO3(6-OSO3)-. 6-oso3 118-124 C-X-C motif chemokine ligand 8 Homo sapiens 11-24 9609743-0 1998 Leukotriene B4 mediates histamine induction of NF-kappaB and IL-8 in human bronchial epithelial cells. Leukotriene B4 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 9660302-8 1998 In the first set of experiments, IL-8 gene reporter constructs were used to transiently transfect a derivative (MVh2E1-9) of the HepG2 cell line which expresses P-4502E1 and metabolizes ethanol. Ethanol 186-193 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 9660302-10 1998 This system may be useful to assess the effects of ethanol on TNF-induced hepatocyte IL-8 production. Ethanol 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 9609743-0 1998 Leukotriene B4 mediates histamine induction of NF-kappaB and IL-8 in human bronchial epithelial cells. Histamine 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 9609743-1 1998 In 16HBE transformed human bronchial epithelial cells, histamine stimulated interleukin (IL)-8 mRNA and protein secretion, and this histamine stimulation was inhibited by the H1-receptor antagonist diphenhydramine (DPH), by the inhibitor of 5-lipoxygenase-activating protein (FLAP) MK-886, by the 5-lipoxygenase inhibitor Zileuton, and by dexamethasone. Histamine 55-64 C-X-C motif chemokine ligand 8 Homo sapiens 76-94 9609743-1 1998 In 16HBE transformed human bronchial epithelial cells, histamine stimulated interleukin (IL)-8 mRNA and protein secretion, and this histamine stimulation was inhibited by the H1-receptor antagonist diphenhydramine (DPH), by the inhibitor of 5-lipoxygenase-activating protein (FLAP) MK-886, by the 5-lipoxygenase inhibitor Zileuton, and by dexamethasone. Diphenhydramine 198-213 C-X-C motif chemokine ligand 8 Homo sapiens 76-94 9609743-1 1998 In 16HBE transformed human bronchial epithelial cells, histamine stimulated interleukin (IL)-8 mRNA and protein secretion, and this histamine stimulation was inhibited by the H1-receptor antagonist diphenhydramine (DPH), by the inhibitor of 5-lipoxygenase-activating protein (FLAP) MK-886, by the 5-lipoxygenase inhibitor Zileuton, and by dexamethasone. Diphenhydramine 215-218 C-X-C motif chemokine ligand 8 Homo sapiens 76-94 9609743-3 1998 Histamine stimulated IL-8 luciferase reporter gene activity that was inhibited with DPH, dexamethasone, MK-886 and L-655,238, and Zileuton. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 9620522-0 1998 The effect of midazolam and propofol on interleukin-8 from human polymorphonuclear leukocytes. Midazolam 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 9609743-3 1998 Histamine stimulated IL-8 luciferase reporter gene activity that was inhibited with DPH, dexamethasone, MK-886 and L-655,238, and Zileuton. Diphenhydramine 84-87 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 9620522-0 1998 The effect of midazolam and propofol on interleukin-8 from human polymorphonuclear leukocytes. Propofol 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 9609743-3 1998 Histamine stimulated IL-8 luciferase reporter gene activity that was inhibited with DPH, dexamethasone, MK-886 and L-655,238, and Zileuton. Dexamethasone 89-102 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 9620522-6 1998 Lipopolysaccharide increased extracellular accumulation of interleukin-8, which was suppressed by both propofol (P = 0.025) and midazolam (P = 0.028). Propofol 103-111 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 9620522-6 1998 Lipopolysaccharide increased extracellular accumulation of interleukin-8, which was suppressed by both propofol (P = 0.025) and midazolam (P = 0.028). Midazolam 128-137 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 9609743-3 1998 Histamine stimulated IL-8 luciferase reporter gene activity that was inhibited with DPH, dexamethasone, MK-886 and L-655,238, and Zileuton. zileuton 130-138 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 9620522-8 1998 Northern blot analysis also revealed increased IL-8 mRNA levels in the presence of both midazolam and propofol, which was confirmed by molecular imaging. Midazolam 88-97 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9609743-4 1998 The inhibition of IL-8 transcription and protein secretion by FLAP inhibitors and Zileuton was reversed with exogenous LTB4. zileuton 82-90 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 9620522-8 1998 Northern blot analysis also revealed increased IL-8 mRNA levels in the presence of both midazolam and propofol, which was confirmed by molecular imaging. Propofol 102-110 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9620522-12 1998 We investigated the effect of propofol and midazolam on interleukin-8, a neutrophil chemotactic agent in human neutrophils. Midazolam 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 9609743-5 1998 There was increased IL-8 nuclear factor-kappaB (NF-kappaB) DNA-binding activity after histamine stimulation, and this was inhibited by DPH and MK-886. Histamine 86-95 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 9620522-14 1998 This suggests that propofol and midazolam alter interleukin-8 secretion from cells. Propofol 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 9609743-5 1998 There was increased IL-8 nuclear factor-kappaB (NF-kappaB) DNA-binding activity after histamine stimulation, and this was inhibited by DPH and MK-886. Diphenhydramine 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 9620522-14 1998 This suggests that propofol and midazolam alter interleukin-8 secretion from cells. Midazolam 32-41 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 9609743-5 1998 There was increased IL-8 nuclear factor-kappaB (NF-kappaB) DNA-binding activity after histamine stimulation, and this was inhibited by DPH and MK-886. MK-886 143-149 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 9624502-2 1998 Roxithromycin suppressed production of interleukin 8 (IL-8), IL-6, and granulocyte-macrophage colony-stimulating factor. Roxithromycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 9609743-7 1998 Thus histamine stimulation of bronchial epithelial cells involves binding at H1 receptors, production of LTB4, activation of NF-kappaB and increased expression of IL-8. Histamine 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 9620068-10 1998 Furthermore, pyrrolidine dithiocarbamate, a specific inhibitor of NF-kappaB activation, prevented the induction of the IL-8 gene, but not that of the VEGF gene. pyrrolidine dithiocarbamic acid 13-40 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 9624502-2 1998 Roxithromycin suppressed production of interleukin 8 (IL-8), IL-6, and granulocyte-macrophage colony-stimulating factor. Roxithromycin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9683032-12 1998 CONCLUSIONS: These studies identify requirements for selectins, beta2 integrins, IL-1 and a rat chemokine(s) similar to human IL-8 for neutrophil recruitment during glycogen-induced peritonitis. Glycogen 165-173 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 9605168-9 1998 Chelerythrin inhibited both the IL-8 and PMA activation of alpha L beta 2 and alpha V beta 3. chelerythrin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 9648711-6 1998 The specific p38 MAP kinase inhibitor, SB 203580, completely inhibited TNF-alpha-, IL-1alpha-, or PAF-induced IL-8 protein and mRNA expression in BECs. SB 203580 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 9629951-7 1998 There were significant and inverse relationships between the availability of plasma tryptophan and serum IL-1RA, IL-6 and IL-8. Tryptophan 84-94 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 9581864-7 1998 Tiludronate suppressed the choline formation induced by NaF, known as an activator of heterotrimeric GTP-binding protein. tiludronic acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 9581864-7 1998 Tiludronate suppressed the choline formation induced by NaF, known as an activator of heterotrimeric GTP-binding protein. Choline 27-34 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 9581864-7 1998 Tiludronate suppressed the choline formation induced by NaF, known as an activator of heterotrimeric GTP-binding protein. Guanosine Triphosphate 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 9581864-9 1998 Tiludronate significantly inhibited the NaF-induced IL-6 secretion in human osteoblastic osteosarcoma Saos-2 cells. tiludronic acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 9665590-3 1998 NF-kappaB involvement was suggested by the finding that pyrrolidinedithiocarbamate, a known inhibitor of NF-kappaB activation, blocked LPS- and IL-1beta-induced IL-8 production. pyrrolidine dithiocarbamic acid 56-82 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 9749983-5 1998 While staurosporin and genistein inhibited both Yersinia invasion and Yersinia-triggered IL-8 secretion, wortmannin, an inhibitor of the phosphatidylinositol-3-phosphate kinase (PI3-K), blocked invasion of Y. enterocolitica into HeLa cells but did not show any effect on IL-8 secretion. Staurosporine 6-18 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 9749983-5 1998 While staurosporin and genistein inhibited both Yersinia invasion and Yersinia-triggered IL-8 secretion, wortmannin, an inhibitor of the phosphatidylinositol-3-phosphate kinase (PI3-K), blocked invasion of Y. enterocolitica into HeLa cells but did not show any effect on IL-8 secretion. Genistein 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 9677630-11 1998 Steroid therapy diminishes the proteins, GM-CSF.RANTES and IL-8 as well as the messengers IL-4, IL-13 and IL-5. Steroids 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 9625374-0 1998 Effect of dehydroepiandrosterone sulfate on interleukin-8 receptor during cervical ripening. Dehydroepiandrosterone Sulfate 10-40 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 9629232-5 1998 Furthermore, we observed that preincubation of monocytes or neutrophils with MET or morphine prevented their subsequent chemotaxis in response to chemokines (MIP1 alpha or IL-8). Morphine 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 9645599-2 1998 Interleukin-8 binds to the glycosaminoglycan (GAG) heparin and the protease inhibitor alpha2-macroglobulin, molecules which regulate the function of a number of cytokines. glycosaminoglycan (gag) heparin 27-58 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9645599-3 1998 Heparan sulphate was previously shown to enhance neutrophil chemotactic responses to IL-8. Heparitin Sulfate 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 9645599-4 1998 OBJECTIVE: The purpose of this study was to investigate the effect of heparin, heparan sulphate and alpha2-macroglobulin on IL-8 binding to neutrophils and subsequent functional effects in vitro. Heparin 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 9645599-4 1998 OBJECTIVE: The purpose of this study was to investigate the effect of heparin, heparan sulphate and alpha2-macroglobulin on IL-8 binding to neutrophils and subsequent functional effects in vitro. Heparitin Sulfate 79-95 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 9645599-7 1998 RESULTS: Heparin, but not heparan sulphate, inhibited the binding of 125I-IL-8 to neutrophils (IC50=26 microg/mL) and IL-8 induced neutrophil chemotactic responses (IC50=4 microg/mL). Heparin 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 9645599-7 1998 RESULTS: Heparin, but not heparan sulphate, inhibited the binding of 125I-IL-8 to neutrophils (IC50=26 microg/mL) and IL-8 induced neutrophil chemotactic responses (IC50=4 microg/mL). Heparin 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 9645599-8 1998 The specific inhibitory effect of heparin was apparently due to an interaction with IL-8 which was charge-dependent, since dextran sulphate had a greater inhibitory effect on chemotactic responses (IC50=2 microg/mL) and FITC-heparin did not bind to neutrophils. Heparin 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9645599-8 1998 The specific inhibitory effect of heparin was apparently due to an interaction with IL-8 which was charge-dependent, since dextran sulphate had a greater inhibitory effect on chemotactic responses (IC50=2 microg/mL) and FITC-heparin did not bind to neutrophils. Dextran Sulfate 123-139 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9645599-8 1998 The specific inhibitory effect of heparin was apparently due to an interaction with IL-8 which was charge-dependent, since dextran sulphate had a greater inhibitory effect on chemotactic responses (IC50=2 microg/mL) and FITC-heparin did not bind to neutrophils. fitc-heparin 220-232 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9645599-9 1998 The heparin-induced inhibition of IL-8 binding and chemotactic responses was reversed in a dose-dependent manner in the presence of alpha2-macroglobulin. Heparin 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9657419-3 1998 There were significant correlations between the availability of tryptophan to the brain and serum IL-6, IL-8 and IL-1RA (all negative) and CC16 (positive). Tryptophan 64-74 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 9625374-1 1998 We investigated the effects of dehydroepiandrosterone sulfate (DHA-S) on the production of interleukin-8 (IL-8) and expression of the interleukin-8 receptor (IL-8 R) in human cervical tissue. Dehydroepiandrosterone Sulfate 31-61 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 9625374-1 1998 We investigated the effects of dehydroepiandrosterone sulfate (DHA-S) on the production of interleukin-8 (IL-8) and expression of the interleukin-8 receptor (IL-8 R) in human cervical tissue. Dehydroepiandrosterone Sulfate 63-68 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 9591504-7 1998 The effect of IL-8 on cell proliferation was examined by tetrazolium bromide and thymidine incorporation. tetrazolium bromide 57-76 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 9625374-1 1998 We investigated the effects of dehydroepiandrosterone sulfate (DHA-S) on the production of interleukin-8 (IL-8) and expression of the interleukin-8 receptor (IL-8 R) in human cervical tissue. Dehydroepiandrosterone Sulfate 63-68 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 9591504-7 1998 The effect of IL-8 on cell proliferation was examined by tetrazolium bromide and thymidine incorporation. Thymidine 81-90 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 9625374-2 1998 DHA-S increased the levels of IL-8 in cultured human cervical fibroblasts and in the supernatant in a time- and dose-dependent manner. Dehydroepiandrosterone Sulfate 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 9625374-3 1998 DHA-S induced IL-8 and IL-8 R expression in human cervical fibroblasts and human pregnant cervical tissue at term in a dose-dependent manner. Dehydroepiandrosterone Sulfate 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 9625374-3 1998 DHA-S induced IL-8 and IL-8 R expression in human cervical fibroblasts and human pregnant cervical tissue at term in a dose-dependent manner. Dehydroepiandrosterone Sulfate 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 9625374-5 1998 However, dehydroepiandrosterone (DHA) only slightly induced the production of IL-8 and the expression of IL-8 R in the same cells and tissue. Dehydroepiandrosterone 9-31 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 9625374-5 1998 However, dehydroepiandrosterone (DHA) only slightly induced the production of IL-8 and the expression of IL-8 R in the same cells and tissue. Dehydroepiandrosterone 9-31 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 9625374-5 1998 However, dehydroepiandrosterone (DHA) only slightly induced the production of IL-8 and the expression of IL-8 R in the same cells and tissue. Dehydroepiandrosterone 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 9625374-5 1998 However, dehydroepiandrosterone (DHA) only slightly induced the production of IL-8 and the expression of IL-8 R in the same cells and tissue. Dehydroepiandrosterone 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 9625374-6 1998 These results suggest that DHA-S up-regulates the autocrine system of IL-8 through the expression of IL-8 R. Dehydroepiandrosterone Sulfate 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 9625374-6 1998 These results suggest that DHA-S up-regulates the autocrine system of IL-8 through the expression of IL-8 R. Dehydroepiandrosterone Sulfate 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 9716261-0 1998 Fosfomycin (FOM: 1 R-2S-epoxypropylphosphonic acid) suppress the production of IL-8 from monocytes via the suppression of neutrophil function. Fosfomycin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 9716261-0 1998 Fosfomycin (FOM: 1 R-2S-epoxypropylphosphonic acid) suppress the production of IL-8 from monocytes via the suppression of neutrophil function. Fosfomycin 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 9716261-0 1998 Fosfomycin (FOM: 1 R-2S-epoxypropylphosphonic acid) suppress the production of IL-8 from monocytes via the suppression of neutrophil function. Fosfomycin 17-50 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 9716261-1 1998 We investigated the influence of fosfomycin (FOM) on the production and the mRNA expression of interleukin-8 (IL-8) by monocytes. Fosfomycin 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 9716261-1 1998 We investigated the influence of fosfomycin (FOM) on the production and the mRNA expression of interleukin-8 (IL-8) by monocytes. Fosfomycin 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 9716261-2 1998 In the incubation of whole blood stimulated by N-Formyl-Met-Leu-Phe (FMLP), FOM significantly suppressed the production and the mRNA expression of IL-8 by monocytes and its inhibitory action was concentration-dependent (FOM: 50-200 microg/ml). N-Formylmethionine Leucyl-Phenylalanine 47-67 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 9574558-10 1998 These findings suggest that TNF-alpha down-regulates CXCR2 expression on PMNs and modulates IL-8-induced biologic responses, leading to the intravascular retention of PMNs with an enhanced production of reactive oxygen metabolites. Oxygen 212-218 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 9713630-7 1998 It was found that CsA inhibits basal secretion of TNF-alpha and IL-8 at 20 and 200 ng ml-1. Cyclosporine 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 9604183-0 1998 Tumor necrosis factor-alpha and interleukin-8 release from U937 human mononuclear cells exposed to zinc oxide in vitro. Zinc Oxide 99-109 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 9604183-2 1998 Respiratory exposure to zinc oxide results in metal fume fever, a flu-like illness characterized by dose-dependent increases in pulmonary tumor necrosis factor-alpha (TNF) and interleukin-8 (IL-8). Zinc Oxide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 176-189 9604183-2 1998 Respiratory exposure to zinc oxide results in metal fume fever, a flu-like illness characterized by dose-dependent increases in pulmonary tumor necrosis factor-alpha (TNF) and interleukin-8 (IL-8). Zinc Oxide 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 9604183-2 1998 Respiratory exposure to zinc oxide results in metal fume fever, a flu-like illness characterized by dose-dependent increases in pulmonary tumor necrosis factor-alpha (TNF) and interleukin-8 (IL-8). Metals 46-51 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 9604183-4 1998 Cell culture supernatant TNF and IL-8 was measured after 3, 8, and 24 hours of exposure to zinc oxide in varying concentrations. Zinc Oxide 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 9604183-8 1998 These data demonstrate that in vitro zinc oxide exposure stimulates U937 mononuclear cells to release TNF and IL-8 consistent with in vivo observations in metal fume fever. Zinc Oxide 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 11774414-1 1998 OBJECTIVE: To identify the nature of the IL-8 inhibitor(s) in gingival crevicul fluid (GCF). 3-[3-[3-[(4~{s})-6-Azanyl-5-Cyano-3-Methyl-4-Propan-2-Yl-2~{h}-Pyrano[2,3-C]pyrazol-4-Yl]-5-(Trifluoromethyl)phenyl]phenyl]propanoic Acid 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 9564285-13 1998 The removal of IL-6 and IL-8 by CVVH after initial stimulation correlates with clinical improvement, which was demonstrated by significantly improved oxygenation and hemodynamics from 2 hours after the initiation of CVVH onward. cvvh 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 11774414-7 1998 RESULTS: (1) IL-8 level in the PMSF-added samples were significantly greater than that in the control group(3.01 mg/L +/- 5.79 mg/L vs 0.05 mg/L +/- 0.15 mg/L, P < 0.001). Phenylmethylsulfonyl Fluoride 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 11774414-8 1998 (2) The mean value of anti-IL-8 IgG in GCF was greater than that of negative control +3 x s. CONCLUSION: A serine protease which can "cleave" IL-8 exists in GCF and GCF from AP sites contain auto-antibody against IL-8. 3-[3-[3-[(4~{s})-6-Azanyl-5-Cyano-3-Methyl-4-Propan-2-Yl-2~{h}-Pyrano[2,3-C]pyrazol-4-Yl]-5-(Trifluoromethyl)phenyl]phenyl]propanoic Acid 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 11774414-8 1998 (2) The mean value of anti-IL-8 IgG in GCF was greater than that of negative control +3 x s. CONCLUSION: A serine protease which can "cleave" IL-8 exists in GCF and GCF from AP sites contain auto-antibody against IL-8. 3-[3-[3-[(4~{s})-6-Azanyl-5-Cyano-3-Methyl-4-Propan-2-Yl-2~{h}-Pyrano[2,3-C]pyrazol-4-Yl]-5-(Trifluoromethyl)phenyl]phenyl]propanoic Acid 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 11774414-8 1998 (2) The mean value of anti-IL-8 IgG in GCF was greater than that of negative control +3 x s. CONCLUSION: A serine protease which can "cleave" IL-8 exists in GCF and GCF from AP sites contain auto-antibody against IL-8. 3-[3-[3-[(4~{s})-6-Azanyl-5-Cyano-3-Methyl-4-Propan-2-Yl-2~{h}-Pyrano[2,3-C]pyrazol-4-Yl]-5-(Trifluoromethyl)phenyl]phenyl]propanoic Acid 157-160 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 11774414-8 1998 (2) The mean value of anti-IL-8 IgG in GCF was greater than that of negative control +3 x s. CONCLUSION: A serine protease which can "cleave" IL-8 exists in GCF and GCF from AP sites contain auto-antibody against IL-8. 3-[3-[3-[(4~{s})-6-Azanyl-5-Cyano-3-Methyl-4-Propan-2-Yl-2~{h}-Pyrano[2,3-C]pyrazol-4-Yl]-5-(Trifluoromethyl)phenyl]phenyl]propanoic Acid 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 11774414-8 1998 (2) The mean value of anti-IL-8 IgG in GCF was greater than that of negative control +3 x s. CONCLUSION: A serine protease which can "cleave" IL-8 exists in GCF and GCF from AP sites contain auto-antibody against IL-8. 3-[3-[3-[(4~{s})-6-Azanyl-5-Cyano-3-Methyl-4-Propan-2-Yl-2~{h}-Pyrano[2,3-C]pyrazol-4-Yl]-5-(Trifluoromethyl)phenyl]phenyl]propanoic Acid 157-160 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 11774414-8 1998 (2) The mean value of anti-IL-8 IgG in GCF was greater than that of negative control +3 x s. CONCLUSION: A serine protease which can "cleave" IL-8 exists in GCF and GCF from AP sites contain auto-antibody against IL-8. 3-[3-[3-[(4~{s})-6-Azanyl-5-Cyano-3-Methyl-4-Propan-2-Yl-2~{h}-Pyrano[2,3-C]pyrazol-4-Yl]-5-(Trifluoromethyl)phenyl]phenyl]propanoic Acid 157-160 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 9531596-4 1998 We show that ATRA selectively inhibited LPS induction of TF expression in human monocytes and monocytic THP-1 cells without affecting LPS induction of tumor necrosis factor-alpha (TNF-alpha) and interleukin-8 (IL-8). Tretinoin 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 9554339-11 1998 BCG induced IL-8 release was further enhanced in the presence of indomethacin. Indomethacin 65-77 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 9547339-6 1998 15R/S-methyl-LXA4 and 16-phenoxy-LXA4 each attenuated (IC50 approximately 10 nM) IL-8 release. 15r 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 9547339-6 1998 15R/S-methyl-LXA4 and 16-phenoxy-LXA4 each attenuated (IC50 approximately 10 nM) IL-8 release. s-methyl-lxa4 4-17 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 9547339-6 1998 15R/S-methyl-LXA4 and 16-phenoxy-LXA4 each attenuated (IC50 approximately 10 nM) IL-8 release. 16-phenoxy-lxa4 22-37 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 9564459-1 1998 The purpose of this study was to examine the association between experimental rhinovirus infection and the elaboration of interleukin-8 (IL-8) into nasal secretions of volunteers and to determine the effect of pentoxifylline on IL-8 elaboration and rhinovirus-associated common cold symptoms. Pentoxifylline 210-224 C-X-C motif chemokine ligand 8 Homo sapiens 228-232 9558006-4 1998 Here, we present research examining paclitaxel"s ability to alter expression of the interleukin-1beta (IL-1beta) and IL-8 cytokines in primary human monocytes, T lymphocytes, and four human breast cancer cell lines: MCF-7, ZR-75-1, MDA-MB-468, and MDA-MB-231. Paclitaxel 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 9566351-1 1998 The present studies demonstrate that histamine induces the secretion of IL-6, IL-8 and GM-CSF from human conjunctival epithelial cells in a dose- and time-dependent manner. Histamine 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 9584909-3 1998 Triclosan is used in dentifrices in combination with either zinc citrate or sodium fluoride (NaF). Triclosan 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 9584909-3 1998 Triclosan is used in dentifrices in combination with either zinc citrate or sodium fluoride (NaF). Sodium Fluoride 76-91 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 9566351-3 1998 Emedastine potently inhibited histamine-induced IL-6, IL-8 and GM-CSF secretion with mean IC50 values of 2.23, 3.42 and 1.50 nM, respectively. emedastine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9628260-5 1998 RESULTS: Anthralin, at concentrations between 5 microM and 25 microM, caused a marked increase in granulocyte macrophage-colony stimulating factor (GM-CSF), interleukin (IL)-6, IL-8 and TNFalpha synthesis that was selectively inhibited by specific antioxidants. Anthralin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 9566351-3 1998 Emedastine potently inhibited histamine-induced IL-6, IL-8 and GM-CSF secretion with mean IC50 values of 2.23, 3.42 and 1.50 nM, respectively. Histamine 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9534964-5 1998 Furthermore, associated with this reduced expression of IL-8 receptors was impairment of both intracellular calcium flux and migration of PMNL in response to IL-8 in a group of HIV/TB patients compared with that in healthy persons. Calcium 108-115 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 9641099-0 1998 Fluoride release from three different types of glass ionomer cements after exposure to NaF solution and APF gel. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 9641099-8 1998 As a result we conclude that glass ionomer cements can act as a rechargeable slow fluoride release systems and especially in caries active children, topical NaF applications with glass ionomer cements could be recommended as a preventive measure. Fluorides 82-90 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 9543141-6 1998 We then investigated the modulation of endometrial stromal cell IL-8 production and proliferation by antisense oligonucleotides specific for IL-8. Oligonucleotides 111-127 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 9543141-8 1998 IL-8 antisense oligonucleotide treatment decreased IL-8 production by endometrial stromal cells in culture as well as cell proliferation when it is compared with scrambled (nonsense) oligonucleotide treatment (P < 0.01). Oligonucleotides 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9543141-8 1998 IL-8 antisense oligonucleotide treatment decreased IL-8 production by endometrial stromal cells in culture as well as cell proliferation when it is compared with scrambled (nonsense) oligonucleotide treatment (P < 0.01). Oligonucleotides 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 9543141-8 1998 IL-8 antisense oligonucleotide treatment decreased IL-8 production by endometrial stromal cells in culture as well as cell proliferation when it is compared with scrambled (nonsense) oligonucleotide treatment (P < 0.01). Oligonucleotides 183-198 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9543141-9 1998 Addition of IL-8 (1 ng/mL) reversed the proliferation inhibitory effect of IL-8 antisense oligonucleotides. Oligonucleotides 90-106 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 9543141-9 1998 Addition of IL-8 (1 ng/mL) reversed the proliferation inhibitory effect of IL-8 antisense oligonucleotides. Oligonucleotides 90-106 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9551411-5 1998 The oral administration of indometacin farnesil (a prodrug that is converted to indomethacin after intestinal absorption) before the injection of IL-8 alleviated the infiltration of neutrophils. indomethacin farnesil 27-47 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 9618706-6 1998 Moreover, histamine induces a significant increase of IL-6 and IL-8 secretion by EC. Histamine 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 9627948-0 1998 Inhibition of interleukin-8 synthesis by intraarticular methotrexate therapy in patients with rheumatoid arthritis. Methotrexate 56-68 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 9627948-4 1998 The intraarticular granulocyte counts and IL-8 levels decreased in all MTX treated patients on day 10-13 and stayed low in those patients who could be re-evaluated after 13 weeks. Methotrexate 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9516436-9 1998 However, the sequence of addition of poly(rU) to a diluted solution of ADP/NaF-treated enzyme had a profound effect on the extent of inhibition. Poly U 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 9516436-9 1998 However, the sequence of addition of poly(rU) to a diluted solution of ADP/NaF-treated enzyme had a profound effect on the extent of inhibition. Adenosine Diphosphate 71-74 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 9516436-10 1998 If the ADP/NaF-treated enzyme was diluted into an assay that lacked poly(rU) and the assay was subsequently initiated with poly(rU), the treated enzyme was not inhibited. Adenosine Diphosphate 7-10 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 9516436-10 1998 If the ADP/NaF-treated enzyme was diluted into an assay that lacked poly(rU) and the assay was subsequently initiated with poly(rU), the treated enzyme was not inhibited. Poly U 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 9516436-10 1998 If the ADP/NaF-treated enzyme was diluted into an assay that lacked poly(rU) and the assay was subsequently initiated with poly(rU), the treated enzyme was not inhibited. Poly U 123-131 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 9516436-12 1998 ATP protected the enzyme from inhibition by ADP/NaF. Adenosine Triphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 9516436-12 1998 ATP protected the enzyme from inhibition by ADP/NaF. Adenosine Diphosphate 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 9516436-13 1998 The stoichiometry between ADP and enzyme monomer in the inhibited enzyme complex was 2, as determined from titration of the ATPase activity ([ADP]/[E] = 2.2) and from the number of radiolabeled ADP bound to the inhibited enzyme ([ADP]/[E] = 1.7) in the presence of excess NaF, MgCl2, and poly(rU). Adenosine Diphosphate 26-29 C-X-C motif chemokine ligand 8 Homo sapiens 272-275 9516436-15 1998 The stoichiometry between (dU)18, a defined oligomeric nucleic acid substituting for poly(rU), and enzyme monomer in the inhibited enzyme complex was estimated to be 1 ([(dU)18/[E] = 1.2) from titration of the ATPase activity in the presence of excess ADP, MgCl2, and NaF. Ruthenium 90-92 C-X-C motif chemokine ligand 8 Homo sapiens 268-271 9516436-15 1998 The stoichiometry between (dU)18, a defined oligomeric nucleic acid substituting for poly(rU), and enzyme monomer in the inhibited enzyme complex was estimated to be 1 ([(dU)18/[E] = 1.2) from titration of the ATPase activity in the presence of excess ADP, MgCl2, and NaF. Adenosine Diphosphate 252-255 C-X-C motif chemokine ligand 8 Homo sapiens 268-271 9516436-15 1998 The stoichiometry between (dU)18, a defined oligomeric nucleic acid substituting for poly(rU), and enzyme monomer in the inhibited enzyme complex was estimated to be 1 ([(dU)18/[E] = 1.2) from titration of the ATPase activity in the presence of excess ADP, MgCl2, and NaF. Magnesium Chloride 257-262 C-X-C motif chemokine ligand 8 Homo sapiens 268-271 9510190-3 1998 Full-length Tat (Tat101) enhanced IL-8 transcription through up-regulated transcription factor binding to the CD28-responsive element (CD28RE) in the IL-8 promoter. cd28re 135-141 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9510190-3 1998 Full-length Tat (Tat101) enhanced IL-8 transcription through up-regulated transcription factor binding to the CD28-responsive element (CD28RE) in the IL-8 promoter. cd28re 135-141 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 9551411-7 1998 The TNF-alpha-stimulated expression of IL-8 mRNA and IL-8 production in the cultured synovial cells were markedly inhibited by dexamethasone. Dexamethasone 127-140 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9551411-7 1998 The TNF-alpha-stimulated expression of IL-8 mRNA and IL-8 production in the cultured synovial cells were markedly inhibited by dexamethasone. Dexamethasone 127-140 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9551411-8 1998 In conclusion, IL-8 levels were markedly elevated in the joint fluids of patients with DRA. dra 87-90 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 9551411-9 1998 Interleukin-8 released from synovial cells may be an important factor to induce acute inflammation in DRA. dra 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9551411-10 1998 Dexamethasone and indomethacin may be effective for DRA by inhibiting the production and chemotactic actions of IL-8, respectively. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 9551411-10 1998 Dexamethasone and indomethacin may be effective for DRA by inhibiting the production and chemotactic actions of IL-8, respectively. Indomethacin 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 9559913-6 1998 The PDE4 inhibitor rolipram had limited effect on zymosan-induced IL-8 generation. Zymosan 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 9559913-0 1998 Effect of PDE4 inhibitors on zymosan-induced IL-8 release from human neutrophils: synergism with prostanoids and salbutamol. Zymosan 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 9517588-8 1998 Furthermore, the serum IL-8 level showed a negative correlation with important indicators of impairment of lung function (DL(CO), TLC, VC) and PaO2. pao2 143-147 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 9517606-9 1998 Budesonide decreased serum IL-8 from 9.2 +/- 3.7 to 6.2 +/- 2.1 pg/ml (p < 0.001). Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9602633-7 1998 DEX caused dose dependent inhibition of IL-1 induced IL-8 (p < 0.001) and MCP-1 (p < 0.05) secretion and mRNA expression at all concentrations of rIL-1 beta. Dexamethasone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9602633-10 1998 CONCLUSIONS: DEX is a potent inhibitor of OF IL-8 and MCP-1. Dexamethasone 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 9559913-4 1998 In the present study, we examined the effects of cyclic AMP elevating agents on the ability of human neutrophils to generate IL-8 in response to zymosan particles. Cyclic AMP 49-59 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 9559913-7 1998 In contrast, the PDE4 inhibitors RP 73401 and SB 207499 concentration-dependently suppressed IL-8 generation. Cilomilast 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 9559913-4 1998 In the present study, we examined the effects of cyclic AMP elevating agents on the ability of human neutrophils to generate IL-8 in response to zymosan particles. Zymosan 145-152 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Prostaglandins 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Prostaglandins 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Alprostadil 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Alprostadil 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Alprostadil 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Alprostadil 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Dinoprostone 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Dinoprostone 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Zymosan 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Zymosan 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Alprostadil 157-161 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Alprostadil 157-161 C-X-C motif chemokine ligand 8 Homo sapiens 182-186 9559913-11 1998 The prostanoids prostaglandin E1 (PGE1) and PGE2 inhibited zymosan-induced IL-8 release from neutrophils in a dose-dependent manner, in response to 10(-5) M PGE1 and PGE2 inhibiting IL-8 generation by 89% and 75%, respectively. Dinoprostone 166-170 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9559913-12 1998 Similarly, the beta2-adrenoceptor agonist salbutamol also inhibited IL-8 generation, but it was less effective than the prostanoids. Albuterol 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 9559913-14 1998 Significant synergism between prostanoids or salbutamol and the PDE4 inhibitors to inhibit IL-8 generation was observed. Prostaglandins 30-41 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 9559913-14 1998 Significant synergism between prostanoids or salbutamol and the PDE4 inhibitors to inhibit IL-8 generation was observed. Albuterol 45-55 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 9559913-18 1998 Pretreatment of neutrophils with these drugs completely reversed the inhibitory effects of a combination treatment with rolipram and PGE2 on zymosan-induced IL-8 release. Rolipram 120-128 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 9559913-18 1998 Pretreatment of neutrophils with these drugs completely reversed the inhibitory effects of a combination treatment with rolipram and PGE2 on zymosan-induced IL-8 release. Dinoprostone 133-137 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 9559913-18 1998 Pretreatment of neutrophils with these drugs completely reversed the inhibitory effects of a combination treatment with rolipram and PGE2 on zymosan-induced IL-8 release. Zymosan 141-148 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 9559913-23 1998 Thus, our results demonstrate that cyclic AMP-elevating agents modulate the ability of neutrophils to generate IL-8 in response to a particulate stimulus. Cyclic AMP 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 9613677-4 1998 This procedure revealed that T98G cells were the main source and that PA-treated monocytes effectively stimulated IL-8 and MCP-1 production by T98G cells. paraform 70-72 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 9517777-4 1998 RESULTS: Nitric oxide production was partly (< or = 50%) inhibited and IL-8 almost completely suppressed (> 80%) by dexamethasone and methylprednisolone. Dexamethasone 122-135 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 9525460-7 1998 The eosinophil-induced release of IL-8, GM-CSF, and sICAM-1 from the HNEC was significantly attenuated by treatment with fexofenadine. fexofenadine 121-133 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9617859-0 1998 Correlations between interleukin-8, and myeloperoxidase or luminol-dependent chemiluminescence in inflamed mucosa of ulcerative colitis. Luminol 59-66 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 9617859-1 1998 Interleukin-8 (IL-8) is a peptide which induces not only chemotaxis of neutrophils but also the release of reactive oxygen metabolites from the neutrophils. Oxygen 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9617859-1 1998 Interleukin-8 (IL-8) is a peptide which induces not only chemotaxis of neutrophils but also the release of reactive oxygen metabolites from the neutrophils. Oxygen 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 9617859-6 1998 The levels of IL-8 were closely correlated to luminol-dependent chemiluminescence or myeloperoxidase levels. Luminol 46-53 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 9498788-5 1998 The IL-8 produced under these conditions was biologically active as determined in the calcium mobilization assay. Calcium 86-93 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 9517777-4 1998 RESULTS: Nitric oxide production was partly (< or = 50%) inhibited and IL-8 almost completely suppressed (> 80%) by dexamethasone and methylprednisolone. Methylprednisolone 140-158 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 9517777-5 1998 Sulfasalazine in pharmacological concentration and indomethacin slightly increased IL-8. Indomethacin 51-63 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 9517777-7 1998 CONCLUSION: Dexamethasone and methylprednisolone are inhibitors of human chondrocyte nitric oxide production, although to a lesser extent than for IL-8 production. Methylprednisolone 30-48 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 9461540-4 1998 Cycloheximide (CHI, 10 microg/ml), an inhibitor of protein synthesis, maximally increased IL-8 mRNA levels 30-fold in H292 cells. Cycloheximide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 9520946-3 1998 In the present study, we further examined the effects of GHSA on TNF-alpha- and IL-1 beta-induced HRPE IL-8 and monocyte chemoattractant protein (MCP)-1 gene expression and protein secretion in HRPE. ghsa 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 9520946-4 1998 At maximally effective concentrations, GHSA (2000 micrograms/ml) potentiated TNF-alpha (20 ng/ml)-stimulated HRPE IL-8 secretion approximately 7-fold. ghsa 39-43 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 9520946-7 1998 Moreover, potentiation of HRPE IL-8 generation by GHSA appeared to be selective for TNF-alpha because, under similar conditions, GHSA was unable to enhance the IL-1 beta-stimulated IL-8 gene expression and protein secretion. ghsa 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 9583368-0 1998 Glutamine-supplemented total parenteral nutrition reduces blood mononuclear cell interleukin-8 release in severe acute pancreatitis. Glutamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 9583368-7 1998 Glutamine supplementation did not significantly influence TNF or IL-6 release, but, in contrast, median IL-8 release was reduced by day 7 in the glutamine group while it was increased in the conventional group (-17.7 ng/mL (median change over study period) versus +43.3 ng/mL, respectively; P=0.045). Glutamine 145-154 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 9583368-8 1998 Small patient numbers and substantial interindividual variation limit the conclusions, but there is a trend for the glutamine group to have improved lymphocyte proliferation, and in the case of IL-8, reduced proinflammatory cytokine release. Glutamine 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 194-198 9692114-0 1998 N-acetylcysteine inhibits IL-1 alpha-induced IL-8 secretion by bronchial epithelial cells. Acetylcysteine 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 10923535-5 1998 There was significant relationship between maternal serum and amniotic fluid IL8, TNF alpha with the time of the premature rupture of membanes. membanes 134-142 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 9469462-7 1998 Moreover, RIA indicates that the activation of cellular p38 MAP kinase was required for the neutrophil IL-8 production stimulated by granulocyte-macrophage CSF or LPS as well as TNF-alpha, but not for that induced by PMA or ionomycin. Ionomycin 224-233 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 9461540-4 1998 Cycloheximide (CHI, 10 microg/ml), an inhibitor of protein synthesis, maximally increased IL-8 mRNA levels 30-fold in H292 cells. Cycloheximide 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 9480822-4 1998 Moreover, recombinant human [(Ala)-IL-8]77 induced apoptosis in leukemic cell lines such as K562, HL-60, KG-1, U937, THP-1 and Jurkat, but monocyte-derived IL-8 ([(Ser)-IL-8]72) did not. Serine 164-167 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 9552221-10 1998 The total release of (IL-8) interleukin-8 and eicosanoids significantly decreased in patients treated with antibiotic or steroids and antibiotic. Steroids 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 9452482-9 1998 Furthermore, the peptide aldehyde N-acetyl-Leu-Leu-norleucinal, an agent that blocks both IkappaBalpha proteolysis and NF-kappaB subunit translocation, abrogates recombinant human TNFalpha-inducible IL-8 gene transcription. Aldehydes 25-33 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 9452482-9 1998 Furthermore, the peptide aldehyde N-acetyl-Leu-Leu-norleucinal, an agent that blocks both IkappaBalpha proteolysis and NF-kappaB subunit translocation, abrogates recombinant human TNFalpha-inducible IL-8 gene transcription. acetylleucine 34-46 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 9452482-9 1998 Furthermore, the peptide aldehyde N-acetyl-Leu-Leu-norleucinal, an agent that blocks both IkappaBalpha proteolysis and NF-kappaB subunit translocation, abrogates recombinant human TNFalpha-inducible IL-8 gene transcription. Leucine 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 9459261-5 1998 The peroxynitrite donor (SIN-1) caused an increase in both IL-8 accumulation (P = 0.0004) and elastase accumulation (P = 0.007). Peroxynitrous Acid 4-17 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 9459261-9 1998 We investigated the effect of nitric oxide and peroxynitrite on interleukin-8 and elastase release by white cells during inflammation. Peroxynitrous Acid 47-60 C-X-C motif chemokine ligand 8 Homo sapiens 64-90 9459261-10 1998 Nitric oxide and peroxynitrite had marked effects on elastase and interleukin-8, which suggests modulation of the inflammatory response. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 9459261-10 1998 Nitric oxide and peroxynitrite had marked effects on elastase and interleukin-8, which suggests modulation of the inflammatory response. Peroxynitrous Acid 17-30 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 9512898-3 1998 Interleukin 6 (IL-6) and IL-8 production in response to PMA were markedly diminished by the PKC inhibitor staurosporine. Staurosporine 106-119 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 9473840-9 1998 Due to the inherent nonlinearities in the generation of the SA, the NAF is shown to achieve significantly better SA cancellation compared to the LAF. sa 60-62 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 9616381-8 1998 Preincubation with cycloheximide inhibited IL-6 but not IL-8 transcription, and incubation of stimulated cells with actinomycin D stabilized IL-8 and also IL-6 mRNA. Dactinomycin 116-129 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 9552221-10 1998 The total release of (IL-8) interleukin-8 and eicosanoids significantly decreased in patients treated with antibiotic or steroids and antibiotic. Steroids 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 28-41 9552221-12 1998 In conclusion, short-term treatment with enteric-coated amoxicillin-clavulanic acid decreases the intraluminal release of IL-8 and other inflammatory mediators. Amoxicillin-Potassium Clavulanate Combination 56-83 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 9513367-3 1998 In patients without methylprednisolone treatment, IL-8 levels in BALF were 362 +/- 67 pg/ml on 0-POD and 948 +/- 359 pg/ml on 1-POD, and were approximately 10 times higher than those in plasma levels. Methylprednisolone 20-38 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 9513367-6 1998 The patients with preoperative methylprednisolone treatment had significantly lower IL-8 levels in BALF and plasma compared with the patients without the treatment. Methylprednisolone 31-49 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9635030-0 1998 Taurine chloramine inhibits the production of superoxide anion, IL-6 and IL-8 in activated human polymorphonuclear leukocytes. N-chlorotaurine 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 9537674-4 1998 RESULTS: There was a significant inhibition by dexamethasone (from 1 to 100 nM) on the secretion of monokines (IL-1beta, IL-6, IL-8 and TNF alpha) and lymphokines (IL-2, IL-4, IL-10 and IFN gamma), either after LPS or PHA stimulation (P < 0.01). Dexamethasone 47-60 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 10095866-0 1998 Effect of roxithromycin on IL-8 synthesis and proliferation of nasal polyp fibroblasts. Roxithromycin 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9583095-6 1998 We also found a negative correlation between the expression of IL-8 mRNA and creatinine clearance. Creatinine 77-87 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 9598103-6 1998 The formation of dUTP from dCyd, was also enhanced by NaF, in parallel of dCK potentiation. deoxyuridine triphosphate 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 9917534-7 1998 In conclusion, the reduction in TNF-alpha, IL-6 and IL-8 was most impressive with the polyacrylonitrile membrane after 4 h of hemofiltration and was largely due to adsorption. polyacrylonitrile 86-103 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 9448049-6 1998 IL-8 release induced by TNF-alpha and IFN-gamma was partly inhibited by the Th-2-derived cytokines IL-4, IL-10, and IL-13, as well as by dexamethasone. Dexamethasone 137-150 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9536224-0 1998 RANTES expression in psoriatic skin, and regulation of RANTES and IL-8 production in cultured epidermal keratinocytes by active vitamin D3 (tacalcitol). Cholecalciferol 128-138 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 9536224-0 1998 RANTES expression in psoriatic skin, and regulation of RANTES and IL-8 production in cultured epidermal keratinocytes by active vitamin D3 (tacalcitol). 1 alpha,24-dihydroxyvitamin D3 140-150 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 9536224-13 1998 Tacalcitol (1 alpha,24(R)-dihydroxyvitamin D3), an active vitamin D3 analogue, inhibited RANTES and IL-8 production in cultured normal epidermal keratinocytes. 1 alpha,24-dihydroxyvitamin D3 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 9536224-13 1998 Tacalcitol (1 alpha,24(R)-dihydroxyvitamin D3), an active vitamin D3 analogue, inhibited RANTES and IL-8 production in cultured normal epidermal keratinocytes. 1 alpha,24-dihydroxyvitamin D3 12-45 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 9536224-13 1998 Tacalcitol (1 alpha,24(R)-dihydroxyvitamin D3), an active vitamin D3 analogue, inhibited RANTES and IL-8 production in cultured normal epidermal keratinocytes. Cholecalciferol 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 9536226-0 1998 Calcipotriene-induced improvement in psoriasis is associated with reduced interleukin-8 and increased interleukin-10 levels within lesions. calcipotriene 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 9536226-12 1998 Calcipotriene-induced clinical improvement of psoriasis is preceded by an increase in IL-10 and a concomitant decrease in IL-8 levels. calcipotriene 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 14517454-7 1998 An angiogenic factor, interleukin 8, was dramatically induced in vascular endothelial cells treated with doxorubicin, but not in cells treated with cisplatin. Doxorubicin 105-116 C-X-C motif chemokine ligand 8 Homo sapiens 22-35 14517454-8 1998 Co-administration of anti-interleukin 8 antibody almost completely blocked the doxorubicin-induced angiogenesis in vitro, suggesting a paracrine/autocrine control through drug-induced angiogenic factor(s). Doxorubicin 79-90 C-X-C motif chemokine ligand 8 Homo sapiens 26-39 9917534-5 1998 The progressive decrease in cytokine concentrations was identical between the two filtration modes and most pronounced with the polyacrylonitrile membrane (reduction 77% for IL-6, 39% for TNF-alpha and 95% for IL-8 after 4 h of hemofiltration). polyacrylonitrile 128-145 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 9473671-6 1998 Glutathione depletion also potentiated the inhibition by H2O2 of carbachol- or G-protein (NaF)-stimulated phosphoinositide hydrolysis, whereas phospholipase C activated by the calcium ionophore ionomycin was not inhibited. Glutathione 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 9473671-6 1998 Glutathione depletion also potentiated the inhibition by H2O2 of carbachol- or G-protein (NaF)-stimulated phosphoinositide hydrolysis, whereas phospholipase C activated by the calcium ionophore ionomycin was not inhibited. Phosphatidylinositols 106-122 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 9523735-2 1998 In addition to its cytotoxic effects on ovarian cancer cells, taxol can transcriptionally activate genes such as IL-8 that may play a role in tumorigenesis. Paclitaxel 62-67 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 9473671-6 1998 Glutathione depletion also potentiated the inhibition by H2O2 of carbachol- or G-protein (NaF)-stimulated phosphoinositide hydrolysis, whereas phospholipase C activated by the calcium ionophore ionomycin was not inhibited. Calcium 176-183 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 9473671-6 1998 Glutathione depletion also potentiated the inhibition by H2O2 of carbachol- or G-protein (NaF)-stimulated phosphoinositide hydrolysis, whereas phospholipase C activated by the calcium ionophore ionomycin was not inhibited. Ionomycin 194-203 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 9473671-7 1998 The thiol-oxidizing agent diamide also inhibited phosphoinositide hydrolysis stimulated by carbachol or NaF, and glutathione depletion potentiated the diamide concentration-dependent inhibition. Sulfhydryl Compounds 4-9 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 9473671-7 1998 The thiol-oxidizing agent diamide also inhibited phosphoinositide hydrolysis stimulated by carbachol or NaF, and glutathione depletion potentiated the diamide concentration-dependent inhibition. Diamide 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 9473671-7 1998 The thiol-oxidizing agent diamide also inhibited phosphoinositide hydrolysis stimulated by carbachol or NaF, and glutathione depletion potentiated the diamide concentration-dependent inhibition. Phosphatidylinositols 49-65 C-X-C motif chemokine ligand 8 Homo sapiens 104-107 9473671-6 1998 Glutathione depletion also potentiated the inhibition by H2O2 of carbachol- or G-protein (NaF)-stimulated phosphoinositide hydrolysis, whereas phospholipase C activated by the calcium ionophore ionomycin was not inhibited. Hydrogen Peroxide 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 9588080-0 1998 [Production of IL-8 by the THP-1 monocyte cell line is regulated differently by cyclosporin and retinoic acid]. Cyclosporine 80-91 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 9588080-0 1998 [Production of IL-8 by the THP-1 monocyte cell line is regulated differently by cyclosporin and retinoic acid]. Tretinoin 96-109 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 9588080-7 1998 The aim of the experiment was to find out CsA effect and RA effect on production of IL-8 by THP-1 cell line. Cyclosporine 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9588080-7 1998 The aim of the experiment was to find out CsA effect and RA effect on production of IL-8 by THP-1 cell line. Tretinoin 57-59 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9588080-11 1998 It was found out that CsA inhibits IL-8 production by stimulated THP-1 monocyte cell line in dose dependence course. Cyclosporine 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 9588080-12 1998 RA promotes IL-8 production by stimulated THP-1 monocyte cell line in dose dependence course. Tretinoin 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 9523735-3 1998 Utilizing IL-8 as a prototypic marker of tumor-derived modulators of growth, we undertook a systematic study of taxol and 11 structurally modified taxol analogs to identify the region of the taxane skeleton responsible for IL-8 gene induction. taxane 191-197 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 9523735-3 1998 Utilizing IL-8 as a prototypic marker of tumor-derived modulators of growth, we undertook a systematic study of taxol and 11 structurally modified taxol analogs to identify the region of the taxane skeleton responsible for IL-8 gene induction. taxane 191-197 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 9523735-5 1998 IL-8 gene induction was assessed by Northern blot analysis after 6 h and cytotoxicity after 72 h. RESULTS: Changes in the southern hemisphere (C-1 to C-4) of the taxane skeleton had greater effects on IL-8 induction than changes in the northern hemisphere (C-7 to C-11). taxane 162-168 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9523735-5 1998 IL-8 gene induction was assessed by Northern blot analysis after 6 h and cytotoxicity after 72 h. RESULTS: Changes in the southern hemisphere (C-1 to C-4) of the taxane skeleton had greater effects on IL-8 induction than changes in the northern hemisphere (C-7 to C-11). taxane 162-168 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 9523735-6 1998 Some of the taxol analogs modified at positions C-1 and/or C-2 with increased hydrophobicity induced IL-8 expression more than threefold over that induced by taxol or taxotere and more than 20-fold over control cells. Paclitaxel 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 9444409-6 1998 The level of IL-8 was significantly higher in the lavage fluid of patients with uterine endometritis than in the controls (p < 0.001), and decreased by CAM treatment (p < 0.01). Clarithromycin 155-158 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 9523735-6 1998 Some of the taxol analogs modified at positions C-1 and/or C-2 with increased hydrophobicity induced IL-8 expression more than threefold over that induced by taxol or taxotere and more than 20-fold over control cells. Paclitaxel 158-163 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 9523735-6 1998 Some of the taxol analogs modified at positions C-1 and/or C-2 with increased hydrophobicity induced IL-8 expression more than threefold over that induced by taxol or taxotere and more than 20-fold over control cells. Docetaxel 167-175 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 9537772-11 1998 In contrast, hydrocortisone, but not cetirizine, reduced GM-CSF and IL-8 release. Hydrocortisone 13-27 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 9701662-3 1998 Hydrolysis in low NaF concentrations results in the formation of discrete fluorapatite crystals on the surfaces of the CaHPO4 crystallites. fluorapatite 74-86 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 9701662-3 1998 Hydrolysis in low NaF concentrations results in the formation of discrete fluorapatite crystals on the surfaces of the CaHPO4 crystallites. calcium phosphate, dibasic, anhydrous 119-125 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 9701662-4 1998 At CaHPO4/NaF molar ratios from approximately 9:1 to 10:2, fluorapatite formed in approximately 3 h as the only crystalline product and complete hydrolysis of CaHPO4 occurred; a pH value as low as 2.4 was attained with solution species being predominantly sodium phosphate. fluorapatite 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 9701662-4 1998 At CaHPO4/NaF molar ratios from approximately 9:1 to 10:2, fluorapatite formed in approximately 3 h as the only crystalline product and complete hydrolysis of CaHPO4 occurred; a pH value as low as 2.4 was attained with solution species being predominantly sodium phosphate. calcium phosphate, dibasic, anhydrous 159-165 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 9701662-4 1998 At CaHPO4/NaF molar ratios from approximately 9:1 to 10:2, fluorapatite formed in approximately 3 h as the only crystalline product and complete hydrolysis of CaHPO4 occurred; a pH value as low as 2.4 was attained with solution species being predominantly sodium phosphate. sodium phosphate 256-272 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 9701662-5 1998 At NaF concentrations beyond those which result in pH minima, fluorapatite and CaF2 are the crystalline products. fluorapatite 62-74 C-X-C motif chemokine ligand 8 Homo sapiens 3-6 9701662-6 1998 At 0.6 M NaF, pseudomorphs composed of fluorapatite and CaF2 crystals form without developing morphologies characteristic of individual fluorapatite and CaF2 crystals. fluorapatite 39-51 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 9701662-7 1998 CaHPO2 can hydrolyze completely to fluorapatite and CaF2 within a few hours depending on NaF concentration and liquid-to-solids ratio. cahpo2 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 9701662-7 1998 CaHPO2 can hydrolyze completely to fluorapatite and CaF2 within a few hours depending on NaF concentration and liquid-to-solids ratio. fluorapatite 35-47 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 9434794-6 1998 After exposure of human monocytes to HOCl-LDL, it was found that mRNA and protein of the chemokine IL-8 was strongly induced, while the chemokine MCP-1 was not. Hypochlorous Acid 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 9472473-6 1998 RESULTS: GHSA at 500 micrograms/ml concentration induced a significant increase in keratocyte IL-8 and MCP-1 protein secretion over the 24 h time course. ghsa 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 9472473-9 1998 The levels of GHSA (500 micrograms/ml)-induced keratocyte IL-8 and MCP-1 expression were similar to that induced by IL-1 beta (0.02 ng/ml) and TNF-alpha (2.0 ng/ml). ghsa 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 9419178-0 1998 Effects of nitric oxide on chemotaxis and endotoxin-induced interleukin-8 production in human neutrophils. Nitric Oxide 11-23 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 9543278-9 1998 Treatment of DPB with macrolides for 6 months significantly reduced neutrophil count and concentrations of defensins and IL-8 in BALF. Macrolides 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 9506829-0 1998 Stimulation of interleukin-8 production by acidic polysaccharides from the root of Panax ginseng. Polysaccharides 50-65 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 9506829-5 1998 We found that one component, ginsenan S-IIA, is a potent inducer of IL-8 production by human monocytes and THP-1 cells, and this induction is accompanied by increased IL-8 mRNA expression. ginsenan 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 9506829-5 1998 We found that one component, ginsenan S-IIA, is a potent inducer of IL-8 production by human monocytes and THP-1 cells, and this induction is accompanied by increased IL-8 mRNA expression. ginsenan 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 9552003-7 1998 In contrast, while IL-8 production in response to S. cerevisiae and zymosan was enhanced in the presence of TNF-alpha, no MIP-1alpha was produced. Zymosan 68-75 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 9485196-2 1998 It shares CXCR2 with all neutrophil-activating chemokines, which like IL-8 have a conserved Glu-Leu-Arg (ELR) N-terminal motif, but is generally considered to be the only relevant agonist for CXCR1. Glutamic Acid 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 9485196-2 1998 It shares CXCR2 with all neutrophil-activating chemokines, which like IL-8 have a conserved Glu-Leu-Arg (ELR) N-terminal motif, but is generally considered to be the only relevant agonist for CXCR1. Leucine 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 9485196-2 1998 It shares CXCR2 with all neutrophil-activating chemokines, which like IL-8 have a conserved Glu-Leu-Arg (ELR) N-terminal motif, but is generally considered to be the only relevant agonist for CXCR1. Arginine 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 9485196-3 1998 IL-8 has a basic residue at the sixth position after the second cysteine, which was suggested to contribute to CXCR1 specificity. Cysteine 64-72 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9449504-4 1998 Dexamethasone (DEX) inhibited both generation and secretion of IL-8 in a dose-dependent fashion. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 9449504-4 1998 Dexamethasone (DEX) inhibited both generation and secretion of IL-8 in a dose-dependent fashion. Dexamethasone 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 9449504-5 1998 DEX also dampened formyl-methionyl-leucyl-phenylalanine-or ionomycin-induced eosinophil IL-8 production. Dexamethasone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 9449504-5 1998 DEX also dampened formyl-methionyl-leucyl-phenylalanine-or ionomycin-induced eosinophil IL-8 production. Ionomycin 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 9419178-4 1998 However, lipopolysaccharide-induced IL-8 production was increased in a dose-dependent manner by a combination of sodium nitroprusside and N-acetylcysteine (P = .03) or by S-nitrosoglutathione (P = .004). Nitroprusside 113-133 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 9419178-4 1998 However, lipopolysaccharide-induced IL-8 production was increased in a dose-dependent manner by a combination of sodium nitroprusside and N-acetylcysteine (P = .03) or by S-nitrosoglutathione (P = .004). Acetylcysteine 138-154 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 9419178-4 1998 However, lipopolysaccharide-induced IL-8 production was increased in a dose-dependent manner by a combination of sodium nitroprusside and N-acetylcysteine (P = .03) or by S-nitrosoglutathione (P = .004). S-Nitrosoglutathione 171-191 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 9749826-2 1998 A time-dependent and significant production of IL-8 was detected in the extracellular fluid of astrocyte-rich cultured cells at 2, 3 and 6 hrs after treatment with acidified Krebs-HEPES buffer (pH 6.9), although such production did not appear in the fluid of neuron-rich cells. krebs 174-179 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9419178-7 1998 These data suggest that NO does not directly affect neutrophil chemotaxis but may indirectly alter chemotactic responses by increasing IL-8 production via a cGMP-independent pathway. Cyclic GMP 157-161 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 9419203-0 1998 Cryptococcal glucuronoxylomannan induces interleukin (IL)-8 production by human microglia but inhibits neutrophil migration toward IL-8. cryptococcal glucuronoxylomannan 0-32 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 9419203-3 1998 When added directly to the PMNL, GXM (both serotypes) potently blocked PMNL migration toward IL-8. glucuronoxylomannan 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 9419203-5 1998 These findings suggest that GXM can induce IL-8 production in the brain but that GXM in the systemic circulation inhibits migration of PMNL toward IL-8. glucuronoxylomannan 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 10224600-7 1998 RESULTS: Both forms of PGPS and LPS stimulated IL-6 and IL-8 production by human fetal membranes. pgps 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 10224600-8 1998 Of note is that LPS stimulated IL-6 to a greater degree than IL-8, while PGPS stimulated IL-8 to a greater degree than IL-6. pgps 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 9597508-0 1998 [Inhibition of neutrophil-derived IL-8 production caused by EM (erythromycin) 201 derivative: modification of the activities by the 5-position desosamine side chain]. Erythromycin 60-62 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9597508-0 1998 [Inhibition of neutrophil-derived IL-8 production caused by EM (erythromycin) 201 derivative: modification of the activities by the 5-position desosamine side chain]. Erythromycin 64-76 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9597508-0 1998 [Inhibition of neutrophil-derived IL-8 production caused by EM (erythromycin) 201 derivative: modification of the activities by the 5-position desosamine side chain]. desosamine 143-153 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9749826-2 1998 A time-dependent and significant production of IL-8 was detected in the extracellular fluid of astrocyte-rich cultured cells at 2, 3 and 6 hrs after treatment with acidified Krebs-HEPES buffer (pH 6.9), although such production did not appear in the fluid of neuron-rich cells. HEPES 180-185 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9749826-5 1998 The increase of IL-8 in astrocyte-rich cultures induced by acidosis was potentiated by treatment with glutamate, which enhanced the increase of cytosolic Ca2+ levels under acidosis, and was affected by extracellular Ca2+ conditions, by cyclosporine A, an inhibitor of calcineurin, and by trifluoperazine, an inhibitor of phospholipase A2. Glutamic Acid 102-111 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 9749826-5 1998 The increase of IL-8 in astrocyte-rich cultures induced by acidosis was potentiated by treatment with glutamate, which enhanced the increase of cytosolic Ca2+ levels under acidosis, and was affected by extracellular Ca2+ conditions, by cyclosporine A, an inhibitor of calcineurin, and by trifluoperazine, an inhibitor of phospholipase A2. Cyclosporine 236-250 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 9749826-5 1998 The increase of IL-8 in astrocyte-rich cultures induced by acidosis was potentiated by treatment with glutamate, which enhanced the increase of cytosolic Ca2+ levels under acidosis, and was affected by extracellular Ca2+ conditions, by cyclosporine A, an inhibitor of calcineurin, and by trifluoperazine, an inhibitor of phospholipase A2. Trifluoperazine 288-303 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 9749826-6 1998 Significant inhibition of IL-8 production was detected after 6 hrs of pretreatment with trifluoperazine. Trifluoperazine 88-103 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 9432117-0 1998 Butyrate enhances interleukin (IL)-8 secretion by intestinal epithelial cells in response to IL-1beta and lipopolysaccharide. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 18-36 9432117-4 1998 We hypothesized that butyrate may alter the secretion of IL-8 by intestinal epithelial cells in response to stimulation by IL-1beta or lipopolysaccharide. Butyrates 21-29 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9432117-8 1998 Lipopolysaccharide induced the secretion of IL-8 only after Caco-2 cells cells had been cultured with sodium butyrate. Butyric Acid 102-117 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 9432117-9 1998 Furthermore, butyrate significantly enhanced IL-8 secretion by cells stimulated with IL-1beta. Butyrates 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 9460084-7 1998 Addition of CSAIDs to OA-affected cartilage differentially regulates IL-6 and IL-8 production by inhibiting the spontaneous release of IL-6 but not IL-8 in ex vivo conditions. csaids 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 9432117-10 1998 Butyrate also increased IL-8 mRNA accumulation in stimulated Caco-2 cells. Butyrates 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 9460084-7 1998 Addition of CSAIDs to OA-affected cartilage differentially regulates IL-6 and IL-8 production by inhibiting the spontaneous release of IL-6 but not IL-8 in ex vivo conditions. csaids 12-18 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 10660968-3 1998 This study investigates the IL-8 behaviour in stable angina pectoris after myocardial ischaemia induced by dipyridamole (14 patients) and in unstable angina pectoris, Braunwald"s class III (35 patients). Dipyridamole 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 10216370-8 1998 The level of IL-8 in urine (uIL-8) was elevated in patients with acute graft rejection and uIL-8 decreased after antirejection treatment (772 +/- 241 pg/mg cr. Chromium 99-101 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 10216370-16 1998 Patients with higher concentrations of serum creatinine during UTI had high urine levels of IL-8. Creatinine 45-55 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 9646397-2 1998 After two minutes use in vivo, the release of fluoride from the pointed section of a toothpick impregnated in 4% NaF was estimated to 0.15 mg. Toothpicks produced similar or somewhat higher fluoride concentrations in the approximal area compared with other fluoride-containing products, like dentifrice, mouthrinse solution and tablet. Fluorides 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 9646397-3 1998 The mean fluoride concentration in an approximal area treated for two minutes with a toothpick impregnated in 4% NaF was around 11 mM/l. Fluorides 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 9373254-10 1997 MC-sup and HMC-1-sup induced chemotaxis in blood monocytes (Mo) (control: 100% +/- 12% v 2-hour-MC-sup: 463% +/- 38% v HMC-1-sup: 532% +/- 12%), and a monoclonal antibody (MoAb) to MCP-1 (but not MoAb to IL-8) inhibited Mo-chemotaxis induced by MC-sup or HMC-1-sup (39% to 55% inhibition, P < .05). mc-sup 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 9407069-2 1997 In this study, we demonstrate that oxidant stress induced by tumor necrosis factor alpha (TNFalpha) or H2O2 differentially regulates intercellular adhesion molecule-1 (ICAM-1) and interleukin-8 (IL-8) gene expression in endothelial and epithelial cells. Hydrogen Peroxide 103-107 C-X-C motif chemokine ligand 8 Homo sapiens 180-193 9407069-2 1997 In this study, we demonstrate that oxidant stress induced by tumor necrosis factor alpha (TNFalpha) or H2O2 differentially regulates intercellular adhesion molecule-1 (ICAM-1) and interleukin-8 (IL-8) gene expression in endothelial and epithelial cells. Hydrogen Peroxide 103-107 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 9407069-4 1997 In contrast, H2O2 selectively induced only ICAM-1 in HMEC-1 and only IL-8 in A549. Hydrogen Peroxide 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 9407069-8 1997 The increased neutrophil motility stimulated by conditioned media from H2O2- or TNFalpha-exposed A549 cells was completely inhibited by an anti-IL-8 antibody. Hydrogen Peroxide 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 9408252-7 1997 Production of both IL-6 and IL-8 was stimulated in a concentration-dependent fashion by interleukin-1beta (0.1-10 ng/ml), tumor necrosis factor-alpha (1-100 ng/ml), and bacterial lipopolysaccharide (0.1-10 microg/ml), and also by 100 nM phorbol 12-myristate 13-acetate. Tetradecanoylphorbol Acetate 237-268 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 9459309-9 1997 We found that among various sphingosine derivatives, Sph-1-P specifically inhibited the IL-8- or fLMP-induced chemotactic migration of neutrophils at concentrations below 1 microM. Sphingosine 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 9398246-1 1997 CXCR2 is a seven-transmembrane receptor that transduces intracellular signals in response to the chemokines IL-8, MGSA/GRO, and other ELR motif-containing CXC chemokines by coupling to heterotrimeric GTP-binding proteins. Guanosine Triphosphate 200-203 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 9373254-10 1997 MC-sup and HMC-1-sup induced chemotaxis in blood monocytes (Mo) (control: 100% +/- 12% v 2-hour-MC-sup: 463% +/- 38% v HMC-1-sup: 532% +/- 12%), and a monoclonal antibody (MoAb) to MCP-1 (but not MoAb to IL-8) inhibited Mo-chemotaxis induced by MC-sup or HMC-1-sup (39% to 55% inhibition, P < .05). hmc-1-sup 11-20 C-X-C motif chemokine ligand 8 Homo sapiens 204-208 9366309-6 1997 RESULTS: After 2 weeks to 1 month of oral L-arginine treatment, urinary levels of nitric oxide synthase related enzymes and products increased significantly, while levels of the cytokine IL-8 were not changed significantly. Arginine 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 21160545-4 1997 We observed that the principal benzene metabolites, represented by hydroquinone, 1,4-benzoquinone, phenol, 1,2,4-benzenetriol, and catechol, significantly alters the production of transforming growth factor of (TGF)-alpha and interleukin (IL)-8 in human epidermal keratinocyte cultures. Benzene 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 226-244 21160545-4 1997 We observed that the principal benzene metabolites, represented by hydroquinone, 1,4-benzoquinone, phenol, 1,2,4-benzenetriol, and catechol, significantly alters the production of transforming growth factor of (TGF)-alpha and interleukin (IL)-8 in human epidermal keratinocyte cultures. hydroquinone 67-79 C-X-C motif chemokine ligand 8 Homo sapiens 226-244 9400825-1 1997 Priming of polymorphonuclear neutrophils (PMN) in whole blood (by tumor necrosis factor alpha and interleukin-8 for enhancement of luminol-dependent chemiluminescence induced by human complement-opsonized zymosan) was stable for 120 min. Luminol 131-138 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 9404762-10 1997 Treatment of DPB patients with macrolides significantly reduced the serum levels of these soluble adhesion molecules and BALF concentrations of IL-1 beta and IL-8. Macrolides 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 9412820-7 1997 In addition, both PGE1 and SM-6 increased production of TGF-beta 1, IL-8 and IL-6 and levels of cAMP in both cell types. Alprostadil 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 9412820-7 1997 In addition, both PGE1 and SM-6 increased production of TGF-beta 1, IL-8 and IL-6 and levels of cAMP in both cell types. SM 10906 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 21160545-7 1997 Binary combinations of selected benzene metabolites synergized in the induction of IL-8, while benzene, by itself, induced about a three-fold increase in IL-8 production. Benzene 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 21160545-7 1997 Binary combinations of selected benzene metabolites synergized in the induction of IL-8, while benzene, by itself, induced about a three-fold increase in IL-8 production. Benzene 95-102 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 9400833-3 1997 Their use allowed us to observe that Cbl was tyrosine phosphorylated in response to some (FcgammaRII ligation, opsonized bacteria and zymosan, granulocyte-macrophage colony-stimulating factor, monosodium urate, and calcium pyrophosphate microcrystals), but not all (fMet-Leu-Phe, interleukin-8) neutrophil agonists. Tyrosine 45-53 C-X-C motif chemokine ligand 8 Homo sapiens 280-293 9396683-0 1997 Inhibitory effect of macrolides on interleukin-8 secretion from cultured human nasal epithelial cells. Macrolides 21-31 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 9396683-2 1997 The authors studied the effect of macrolides on interleukin (IL)-8 secretion from cultured human nasal epithelial cells. Macrolides 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 48-66 9396683-7 1997 These results indicate that macrolide antibiotics may act as an immunomodulator to reduce IL-8 in inflammatory sites and, at least partially, account for the clinically discrepant effects between 14- and 16-membered ring macrolides in long-term low-dose therapy for chronic sinusitis. Macrolides 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 9462189-5 1997 TNF alpha, IL-6, and IL-8 concentrations were significantly related to gestational age and duration of supplemental oxygen; TNF alpha, IL-6, and IL-8 concentrations also correlated with length of time on the ventilator. Oxygen 116-122 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 9368010-3 1997 Using methyl-beta-N-acetylglucosaminide as a substrate, the optimal activity was obtained with 0.1% Triton X-100, 30 mM NaF, 20 mM Mn2+, 5 mM AMP in a 30 mM MOPS (3-(N-morpholino) propanesulfonic acid) buffer at pH 6.7. methyl-beta-n-acetylglucosaminide 6-39 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 9368010-3 1997 Using methyl-beta-N-acetylglucosaminide as a substrate, the optimal activity was obtained with 0.1% Triton X-100, 30 mM NaF, 20 mM Mn2+, 5 mM AMP in a 30 mM MOPS (3-(N-morpholino) propanesulfonic acid) buffer at pH 6.7. Octoxynol 100-112 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 9368010-3 1997 Using methyl-beta-N-acetylglucosaminide as a substrate, the optimal activity was obtained with 0.1% Triton X-100, 30 mM NaF, 20 mM Mn2+, 5 mM AMP in a 30 mM MOPS (3-(N-morpholino) propanesulfonic acid) buffer at pH 6.7. Manganese(2+) 131-135 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 9368010-3 1997 Using methyl-beta-N-acetylglucosaminide as a substrate, the optimal activity was obtained with 0.1% Triton X-100, 30 mM NaF, 20 mM Mn2+, 5 mM AMP in a 30 mM MOPS (3-(N-morpholino) propanesulfonic acid) buffer at pH 6.7. Adenosine Monophosphate 142-145 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 9368010-3 1997 Using methyl-beta-N-acetylglucosaminide as a substrate, the optimal activity was obtained with 0.1% Triton X-100, 30 mM NaF, 20 mM Mn2+, 5 mM AMP in a 30 mM MOPS (3-(N-morpholino) propanesulfonic acid) buffer at pH 6.7. morpholinopropane sulfonic acid 157-161 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 9368010-3 1997 Using methyl-beta-N-acetylglucosaminide as a substrate, the optimal activity was obtained with 0.1% Triton X-100, 30 mM NaF, 20 mM Mn2+, 5 mM AMP in a 30 mM MOPS (3-(N-morpholino) propanesulfonic acid) buffer at pH 6.7. morpholinopropane sulfonic acid 163-200 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 9366432-0 1997 Hamycin inhibits IL-8-induced biologic response by modulating its receptor in human polymorphonuclear neutrophils. hamycin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 9366432-2 1997 We have found that hamycin, an antifungal agent, reduces IL-8-induced migration and binding of 125I-labeled IL-8 to neutrophils by 66 and 75%, respectively. hamycin 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9366432-2 1997 We have found that hamycin, an antifungal agent, reduces IL-8-induced migration and binding of 125I-labeled IL-8 to neutrophils by 66 and 75%, respectively. hamycin 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 9366432-3 1997 Other IL-8-induced biologic functions, such as superoxide generation, intracellular Ca2+ mobilization, and enzyme release were also reduced in hamycin-treated cells by 50 to 75%. Superoxides 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 9366432-3 1997 Other IL-8-induced biologic functions, such as superoxide generation, intracellular Ca2+ mobilization, and enzyme release were also reduced in hamycin-treated cells by 50 to 75%. hamycin 143-150 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 9366432-6 1997 Chemical cross-linking of 125I-labeled IL-8 to its receptor followed by 10% SDS-PAGE analysis and autoradiography showed that the signals in hamycin-treated cells were considerably reduced compared with those in controls. Iodine-125 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9366432-6 1997 Chemical cross-linking of 125I-labeled IL-8 to its receptor followed by 10% SDS-PAGE analysis and autoradiography showed that the signals in hamycin-treated cells were considerably reduced compared with those in controls. hamycin 141-148 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9353345-9 1997 The tyrosine kinase inhibitor, genistein, blocked tyrosine phosphorylation and secretion of interleukin-8, whereas the MAP kinase kinase inhibitor PD98059 partially inhibited secretion of interleukin-8. Tyrosine 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 9353345-9 1997 The tyrosine kinase inhibitor, genistein, blocked tyrosine phosphorylation and secretion of interleukin-8, whereas the MAP kinase kinase inhibitor PD98059 partially inhibited secretion of interleukin-8. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 147-154 C-X-C motif chemokine ligand 8 Homo sapiens 188-201 9354625-9 1997 The endothelial cell binding sites for IL-8, RANTES, and MCP-1 were deduced to be glycosaminoglycans since competition assays showed the biphasic curves and micromolar IC50 values seen in studies with immobilized heparin, and mRNA for known chemokine receptors was not detected. Glycosaminoglycans 82-100 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9354625-9 1997 The endothelial cell binding sites for IL-8, RANTES, and MCP-1 were deduced to be glycosaminoglycans since competition assays showed the biphasic curves and micromolar IC50 values seen in studies with immobilized heparin, and mRNA for known chemokine receptors was not detected. Heparin 213-220 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9354625-12 1997 Removal of glycosaminoglycans from CHO cells expressing chemokine receptors CXCR1, CCR1, or CCR2 resulted in 40-70% decreases in the binding of RANTES, MCP-1, IL-8, and MIP-1alpha. Glycosaminoglycans 11-29 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 9431991-0 1997 1alpha,25-dihydroxyvitamin D3 and a variety of its natural metabolites transcriptionally repress nuclear-factor-kappaB-mediated interleukin-8 gene expression. Calcitriol 0-29 C-X-C motif chemokine ligand 8 Homo sapiens 128-141 9431991-3 1997 1alpha,25-Dihydroxyvitamin D3 (calcitriol) repressed IL-8 promoter activity induced by tumor necrosis factor-alpha (TNF-alpha) by 50%, compared to 30% inhibition using dexamethasone, an effect consistent with its effect on TNF-alpha-induced IL-8 release and IL-8 mRNA levels. Calcitriol 0-29 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9431991-3 1997 1alpha,25-Dihydroxyvitamin D3 (calcitriol) repressed IL-8 promoter activity induced by tumor necrosis factor-alpha (TNF-alpha) by 50%, compared to 30% inhibition using dexamethasone, an effect consistent with its effect on TNF-alpha-induced IL-8 release and IL-8 mRNA levels. Calcitriol 0-29 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 9431991-3 1997 1alpha,25-Dihydroxyvitamin D3 (calcitriol) repressed IL-8 promoter activity induced by tumor necrosis factor-alpha (TNF-alpha) by 50%, compared to 30% inhibition using dexamethasone, an effect consistent with its effect on TNF-alpha-induced IL-8 release and IL-8 mRNA levels. Calcitriol 0-29 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 9431991-3 1997 1alpha,25-Dihydroxyvitamin D3 (calcitriol) repressed IL-8 promoter activity induced by tumor necrosis factor-alpha (TNF-alpha) by 50%, compared to 30% inhibition using dexamethasone, an effect consistent with its effect on TNF-alpha-induced IL-8 release and IL-8 mRNA levels. Calcitriol 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9431991-3 1997 1alpha,25-Dihydroxyvitamin D3 (calcitriol) repressed IL-8 promoter activity induced by tumor necrosis factor-alpha (TNF-alpha) by 50%, compared to 30% inhibition using dexamethasone, an effect consistent with its effect on TNF-alpha-induced IL-8 release and IL-8 mRNA levels. Calcitriol 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 9431991-3 1997 1alpha,25-Dihydroxyvitamin D3 (calcitriol) repressed IL-8 promoter activity induced by tumor necrosis factor-alpha (TNF-alpha) by 50%, compared to 30% inhibition using dexamethasone, an effect consistent with its effect on TNF-alpha-induced IL-8 release and IL-8 mRNA levels. Calcitriol 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 241-245 9431991-4 1997 A variety of vitamin D metabolites caused the same repressive effect on IL-8 promoter activation as calcitriol. Vitamin D 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 9431991-5 1997 However, only those metabolites which were able to transactivate a classical vitamin D response element had the ability to repress IL-8 promoter activation, suggesting that this repression is mediated via vitamin D receptor (VDR). Vitamin D 77-86 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 9431991-6 1997 Furthermore, overexpression of VDR in the parental G-361 cell line enhanced the repressive effect of calcitriol on activation of the IL-8 promoter by either TNF-alpha stimulation or overexpression of the NF-kappaB subunit p65. Calcitriol 101-111 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 9431991-7 1997 Electrophoretic mobility shift assays using nuclear extracts from A3 cells showed that calcitriol decreased the abundance of nuclear factors bound to the NF-kappaB binding site of the IL-8 promoter and this reduced binding of NF-kappaB proteins presumably contributes to its inhibitory action. Calcitriol 87-97 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 9353345-9 1997 The tyrosine kinase inhibitor, genistein, blocked tyrosine phosphorylation and secretion of interleukin-8, whereas the MAP kinase kinase inhibitor PD98059 partially inhibited secretion of interleukin-8. Genistein 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 92-105 9372795-2 1997 Also, it has not been established that incorporation of trimetaphosphate (TMP) improves the anticaries activity of NaF toothpastes. trimetaphosphoric acid 56-72 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 9353042-6 1997 Treatment of PNG with the leukotriene-B4 inhibitor MK-886 prior to stimulation with M. tuberculosis or LAM partially blocked IL-8 and GRO-alpha induction, suggesting involvement of the 5-lipoxygenase pathway in the secretion of these chemokines. Leukotrienes 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 9353042-6 1997 Treatment of PNG with the leukotriene-B4 inhibitor MK-886 prior to stimulation with M. tuberculosis or LAM partially blocked IL-8 and GRO-alpha induction, suggesting involvement of the 5-lipoxygenase pathway in the secretion of these chemokines. MK-886 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 9372795-2 1997 Also, it has not been established that incorporation of trimetaphosphate (TMP) improves the anticaries activity of NaF toothpastes. trimetaphosphoric acid 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 115-118 9372795-13 1997 The mean three-year clinical-only DMFS increment for the subjects using 1500-ppm-NaF pastes was 3.93, which was 6% lower than the corresponding mean of 4.19 for the 1000-ppm-NaF pastes. dmfs 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 9357758-2 1997 We characterized the mechanisms by which hyaluronic acid (HA) regulates interleukin-1beta (IL-1beta), tumor necrosis factor-alpha (TNF-alpha), and interleukin-8 (IL-8) production in human uterine fibroblasts. Hyaluronic Acid 41-56 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 9353419-8 1997 Specificity of action is suggested as IL-1-stimulated interleukin-8 (IL-8) production, which is known to be an NFkappaB-regulated event, was also inhibited by hymenialdisine, whereas IL-1-induced production of vascular endothelial growth factor, a non-NFkappaB-regulated gene, was not affected by exposure to hymenialdisine. hymenialdisine 159-173 C-X-C motif chemokine ligand 8 Homo sapiens 38-67 9353419-8 1997 Specificity of action is suggested as IL-1-stimulated interleukin-8 (IL-8) production, which is known to be an NFkappaB-regulated event, was also inhibited by hymenialdisine, whereas IL-1-induced production of vascular endothelial growth factor, a non-NFkappaB-regulated gene, was not affected by exposure to hymenialdisine. hymenialdisine 159-173 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 9353419-8 1997 Specificity of action is suggested as IL-1-stimulated interleukin-8 (IL-8) production, which is known to be an NFkappaB-regulated event, was also inhibited by hymenialdisine, whereas IL-1-induced production of vascular endothelial growth factor, a non-NFkappaB-regulated gene, was not affected by exposure to hymenialdisine. hymenialdisine 309-323 C-X-C motif chemokine ligand 8 Homo sapiens 38-67 9353419-8 1997 Specificity of action is suggested as IL-1-stimulated interleukin-8 (IL-8) production, which is known to be an NFkappaB-regulated event, was also inhibited by hymenialdisine, whereas IL-1-induced production of vascular endothelial growth factor, a non-NFkappaB-regulated gene, was not affected by exposure to hymenialdisine. hymenialdisine 309-323 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 11189316-4 1997 In biological activity test of IL-8 inhibitor, using pooled GCF taken from 8 AP patients (23 teeth), the results showed that the GCF (without recombinant human IL-8, rhIL-8) caused more white blood cell (WBC) migration than blank control group (physiological saline) did. Sodium Chloride 259-265 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 9344494-0 1997 Cocaine inhibits human endothelial cell IL-8 production: the role of transforming growth factor-beta. Cocaine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 9344494-4 1997 We investigated the effect of cocaine on endothelial cell IL-8 production. Cocaine 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 9344494-6 1997 Cocaine decreased IL-8 production in a dose-responsive manner, and this reduction correlated with down-regulation of IL-8 mRNA expression. Cocaine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 9344494-6 1997 Cocaine decreased IL-8 production in a dose-responsive manner, and this reduction correlated with down-regulation of IL-8 mRNA expression. Cocaine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 9344494-7 1997 Cocaine also increased the production of TGF-beta by EA.hy 926 cells and anti-TGF-beta abrogated the cocaine-mediated decrement of IL-8 production, indicating that cocaine down-regulates endothelial IL-8 production by increasing TGF-beta. Cocaine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 9344494-7 1997 Cocaine also increased the production of TGF-beta by EA.hy 926 cells and anti-TGF-beta abrogated the cocaine-mediated decrement of IL-8 production, indicating that cocaine down-regulates endothelial IL-8 production by increasing TGF-beta. Cocaine 101-108 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 9344494-7 1997 Cocaine also increased the production of TGF-beta by EA.hy 926 cells and anti-TGF-beta abrogated the cocaine-mediated decrement of IL-8 production, indicating that cocaine down-regulates endothelial IL-8 production by increasing TGF-beta. Cocaine 101-108 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 9359732-2 1997 CNI-1493 inhibited lipopolysaccharide (LPS)-induced tumor necrosis factor (TNF)-alpha, interleukin (IL)-1alpha, IL-1beta, IL-6, and IL-8 production whether or not LPS stimulation was enhanced by interferon (IFN)-gamma priming. semapimod 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 9334359-0 1997 Upregulation of interleukin 8 by oxygen-deprived cells in glioblastoma suggests a role in leukocyte activation, chemotaxis, and angiogenesis. Oxygen 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 9334359-8 1997 These results support a model where IL-8 expression is initiated early in astrocytoma development through induction by inflammatory stimuli and later in tumor progression increases due to reduced microenvironmental oxygen pressure. Oxygen 215-221 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 9352014-0 1997 Regulation of interleukin (IL)-6 and IL-8 production in an amnion-derived cell line by cytokines, growth factors, glucocorticoids, and phorbol esters. Phorbol Esters 135-149 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 9352014-6 1997 Basal and cytokine-stimulated IL-6 and IL-8 production was inhibited by dexamethasone at concentrations equal to or greater than 1 nM. Dexamethasone 72-85 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9357758-2 1997 We characterized the mechanisms by which hyaluronic acid (HA) regulates interleukin-1beta (IL-1beta), tumor necrosis factor-alpha (TNF-alpha), and interleukin-8 (IL-8) production in human uterine fibroblasts. Hyaluronic Acid 41-56 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 9357758-2 1997 We characterized the mechanisms by which hyaluronic acid (HA) regulates interleukin-1beta (IL-1beta), tumor necrosis factor-alpha (TNF-alpha), and interleukin-8 (IL-8) production in human uterine fibroblasts. Hyaluronic Acid 58-60 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 9357758-2 1997 We characterized the mechanisms by which hyaluronic acid (HA) regulates interleukin-1beta (IL-1beta), tumor necrosis factor-alpha (TNF-alpha), and interleukin-8 (IL-8) production in human uterine fibroblasts. Hyaluronic Acid 58-60 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 9395111-5 1997 If the globules formed may be described as "calcium fluoride like material", the additional information of this experiment is that, after interaction with neutral solutions, they also contain considerable amounts of NaF. Calcium Fluoride 44-60 C-X-C motif chemokine ligand 8 Homo sapiens 216-219 9383257-3 1997 Histamine is a potent activator of endothelial cells (EC): it induces the expression of P-selectin on the surface of endothelium and the secretion of IL-6 and IL-8. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 9383257-7 1997 L and DCL inhibited significantly IL-6 and IL-8 secretion induced by histamine with a more powerful efficiency of the active metabolite. Histamine 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 9383257-9 1997 Similar results were obtained for IL-8 (IC50 = 0.2 x 10[-6] M for L and 10[-9] M for DCL). des(ethoxycarbonyl)loratadine 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9321519-15 1997 The inhibitors BNPP (360 microM) and NaF (500 microM) inhibited alpha-naphthol formation to 9-10% of control and to 14-20% of control, respectively. 1-naphthol 64-78 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 9335957-3 1997 Cholesterol loading in macrophages was found to induce interleukin-8 expression, suggesting an association between foam cell formation and beta 2-integrin-dependent adhesion of leukocytes. Cholesterol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 9356189-7 1997 Zinc oxide exposure was a statistically significant, dose-dependent predictor of increases in BAL TNF (mean exposure-sham difference +/- SE = 9.5 +/- 3.6 pg/mL, P = 0.02), IL-6 (mean exposure-sham difference +/- SE = 5.5 +/- 1.8 pg/mL, P = 0.009), and IL-8 (mean exposure-sham difference +/- SE = 64.1 +/- 23.9 pg/mL, P = 0.02). Zinc Oxide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 252-256 9338624-7 1997 Bilirubin levels, at day of IL-8 peak, did not differ statistically between mild and severe VOD. Bilirubin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 9344885-7 1997 NHBE cells exposed to ROFA produced significant amounts of IL-8, IL-6, and TNF, as well as mRNAs coding for these cytokines. rofa 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 9349985-6 1997 CsA (1, 5, and 10ng/ml) significantly reduced IL-1 beta-induced IL-8 production (by 32%, 41%, and 48%, respectively), and reduced TNF alpha-induced IL-8 production (by 21%, 42%, and 50%, respectively). Cyclosporine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 9349985-6 1997 CsA (1, 5, and 10ng/ml) significantly reduced IL-1 beta-induced IL-8 production (by 32%, 41%, and 48%, respectively), and reduced TNF alpha-induced IL-8 production (by 21%, 42%, and 50%, respectively). Cyclosporine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 9349985-8 1997 The expression of IL-8 mRNA was also inhibited by CsA. Cyclosporine 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 9357022-19 1997 A negative correlation was recognized between the patient plasma Gln level and the Gln 1000/Gln 500 ratio of the cell culture supernatant IL-8 level (r = -0.73, P = 0.025). Glutamine 65-68 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 9357022-19 1997 A negative correlation was recognized between the patient plasma Gln level and the Gln 1000/Gln 500 ratio of the cell culture supernatant IL-8 level (r = -0.73, P = 0.025). Glutamine 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 9357022-19 1997 A negative correlation was recognized between the patient plasma Gln level and the Gln 1000/Gln 500 ratio of the cell culture supernatant IL-8 level (r = -0.73, P = 0.025). Glutamine 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 9363923-3 1997 IL-8 secretion increased in a time-dependent manner throughout the 24 h of observation; in contrast, EDN release reached a plateau value after 12 h. Furthermore, at least 2 microM ionomycin was necessary for induction of IL-8 secretion, whereas 0.5 microM induced detectable EDN release by eosinophils. Ionomycin 180-189 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9363923-3 1997 IL-8 secretion increased in a time-dependent manner throughout the 24 h of observation; in contrast, EDN release reached a plateau value after 12 h. Furthermore, at least 2 microM ionomycin was necessary for induction of IL-8 secretion, whereas 0.5 microM induced detectable EDN release by eosinophils. Ionomycin 180-189 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 9349985-3 1997 The effects of cyclosporine A (CsA), tacrolimus (FK506), and dexamethasone (DEX) on cytokine-induced production of interleukin (IL)-8 in a human colonic cancer cell line (HT-29) were examined. Cyclosporine 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 115-133 9349985-3 1997 The effects of cyclosporine A (CsA), tacrolimus (FK506), and dexamethasone (DEX) on cytokine-induced production of interleukin (IL)-8 in a human colonic cancer cell line (HT-29) were examined. Tacrolimus 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 115-133 9349985-3 1997 The effects of cyclosporine A (CsA), tacrolimus (FK506), and dexamethasone (DEX) on cytokine-induced production of interleukin (IL)-8 in a human colonic cancer cell line (HT-29) were examined. Tacrolimus 49-54 C-X-C motif chemokine ligand 8 Homo sapiens 115-133 9349985-3 1997 The effects of cyclosporine A (CsA), tacrolimus (FK506), and dexamethasone (DEX) on cytokine-induced production of interleukin (IL)-8 in a human colonic cancer cell line (HT-29) were examined. Dexamethasone 61-74 C-X-C motif chemokine ligand 8 Homo sapiens 115-133 9349985-3 1997 The effects of cyclosporine A (CsA), tacrolimus (FK506), and dexamethasone (DEX) on cytokine-induced production of interleukin (IL)-8 in a human colonic cancer cell line (HT-29) were examined. Dexamethasone 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 115-133 9305861-2 1997 Using a mouse lymphoid cell line transfected with human formyl peptide or interleukin-8 receptors and normal human neutrophils as models, we show that cAMP functions as a gating element on the chemoattractant-induced rho-dependent signaling pathway leading to leukocyte integrin activation and adhesion. Cyclic AMP 151-155 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 9350989-0 1997 Intracellular Ca2+ dependence of nitric oxide mediated enhancement of interleukin-8 secretion in human endothelial cells. Nitric Oxide 33-45 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 9350989-5 1997 Sodium nitroprusside (SNP) and S-nitroso-N-acetyl-DL-penicillamine (SNAP) dose dependently increased IL-8 production in this cell type. Nitroprusside 0-20 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 9350989-5 1997 Sodium nitroprusside (SNP) and S-nitroso-N-acetyl-DL-penicillamine (SNAP) dose dependently increased IL-8 production in this cell type. snap 31-66 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 9350989-5 1997 Sodium nitroprusside (SNP) and S-nitroso-N-acetyl-DL-penicillamine (SNAP) dose dependently increased IL-8 production in this cell type. snap 68-72 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 9350989-11 1997 SKF 96365, which has been shown to block receptor mediated Ca2+ entry, and TMB-8, which blocks intracellular Ca2+ release, both inhibited IL-8 secretion, particularly when TNFalpha was used as a costimulator, indicating that [Ca2+]i changes are important components of IL-8 induction by NO.. 1,2,3,4-tetrahydroisoquinoline-7-sulfonamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 9350989-11 1997 SKF 96365, which has been shown to block receptor mediated Ca2+ entry, and TMB-8, which blocks intracellular Ca2+ release, both inhibited IL-8 secretion, particularly when TNFalpha was used as a costimulator, indicating that [Ca2+]i changes are important components of IL-8 induction by NO.. 1,2,3,4-tetrahydroisoquinoline-7-sulfonamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 269-273 9350989-11 1997 SKF 96365, which has been shown to block receptor mediated Ca2+ entry, and TMB-8, which blocks intracellular Ca2+ release, both inhibited IL-8 secretion, particularly when TNFalpha was used as a costimulator, indicating that [Ca2+]i changes are important components of IL-8 induction by NO.. 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate 75-80 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 9350989-11 1997 SKF 96365, which has been shown to block receptor mediated Ca2+ entry, and TMB-8, which blocks intracellular Ca2+ release, both inhibited IL-8 secretion, particularly when TNFalpha was used as a costimulator, indicating that [Ca2+]i changes are important components of IL-8 induction by NO.. 8-(N,N-diethylamino)octyl-3,4,5-trimethoxybenzoate 75-80 C-X-C motif chemokine ligand 8 Homo sapiens 269-273 9373700-6 1997 Milk from the alcohol group contained an elevated amount of IL-8 as compared with milk from non-smoker controls; however, it did not differ statistically from that of the smoker controls. Alcohols 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9373700-7 1997 Blood from the alcohol group showed an increased level of IL-8 when compared with that from both smoker and non-smoker controls. Alcohols 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 9373700-12 1997 The present study found that alcohol consumption during pregnancy could modulate the production of IL-8 and infiltration of certain leukocytes in milk and blood of postpartum women. Alcohols 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 9316497-6 1997 Staurosporine reduced the downmodulation by low-level IL-8 plus LTB4 or IL-1 beta but not by high-level IL-8 alone. Staurosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9316497-6 1997 Staurosporine reduced the downmodulation by low-level IL-8 plus LTB4 or IL-1 beta but not by high-level IL-8 alone. Staurosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 9360082-5 1997 Levels of HA and IL-8 had good correlation with the level of TB (HA: r = 0.60, p < 0.05; IL-8: r = 0.55, p < 0.05). Bilirubin 61-63 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 9322640-7 1997 Also, we found that incubation of decidual cells with various concentrations of lipoteichoic acid, sialic acid, lipopolysaccharide, and lipid A resulted in significant concentration-dependent increases in decidual cell macrophage inflammatory protein-1 alpha and interleukin-8 production (p < 0.05.) lipoteichoic acid 80-97 C-X-C motif chemokine ligand 8 Homo sapiens 263-276 9322640-7 1997 Also, we found that incubation of decidual cells with various concentrations of lipoteichoic acid, sialic acid, lipopolysaccharide, and lipid A resulted in significant concentration-dependent increases in decidual cell macrophage inflammatory protein-1 alpha and interleukin-8 production (p < 0.05.) N-Acetylneuraminic Acid 99-110 C-X-C motif chemokine ligand 8 Homo sapiens 263-276 9322640-7 1997 Also, we found that incubation of decidual cells with various concentrations of lipoteichoic acid, sialic acid, lipopolysaccharide, and lipid A resulted in significant concentration-dependent increases in decidual cell macrophage inflammatory protein-1 alpha and interleukin-8 production (p < 0.05.) Lipid A 136-143 C-X-C motif chemokine ligand 8 Homo sapiens 263-276 9360082-5 1997 Levels of HA and IL-8 had good correlation with the level of TB (HA: r = 0.60, p < 0.05; IL-8: r = 0.55, p < 0.05). Bilirubin 61-63 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 9271387-0 1997 Identification of tumor-specific paclitaxel (Taxol)-responsive regulatory elements in the interleukin-8 promoter. Paclitaxel 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 9302649-0 1997 1,25-Dihydroxyvitamin D3 and a new analogue, 22-oxacalcitriol, modulate proliferation and interleukin-8 secretion of normal human keratinocytes. Calcitriol 0-24 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 9302649-0 1997 1,25-Dihydroxyvitamin D3 and a new analogue, 22-oxacalcitriol, modulate proliferation and interleukin-8 secretion of normal human keratinocytes. maxacalcitol 45-61 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 9302649-3 1997 The present study was conducted to determine whether a new vitamin D3 analogue, 22-oxacalcitriol, could be effective in inhibiting the proliferation and IL-8 secretion of normal human epidermal keratinocytes. Cholecalciferol 59-69 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 9302649-3 1997 The present study was conducted to determine whether a new vitamin D3 analogue, 22-oxacalcitriol, could be effective in inhibiting the proliferation and IL-8 secretion of normal human epidermal keratinocytes. maxacalcitol 80-96 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 9302649-6 1997 Proliferation of cultured normal human epidermal keratinocytes was inhibited in the presence of 1,25-dihydroxyvitamin D3 at the concentrations of 1 x 10(-8) to 1 x 10(-6) M and 22-oxacalcitriol at concentrations of more than 1 x 10(-9) M at 48 h. IL-8 secretion from normal human epidermal keratinocytes was augmented by TNF-alpha, or synergistically by TNF-alpha and IFN-gamma. Calcitriol 96-120 C-X-C motif chemokine ligand 8 Homo sapiens 247-251 9302649-7 1997 1,25-Dihydroxyvitamin D3 and 22-oxacalcitriol inhibited cytokine-stimulated IL-8 production dose dependently after 24 h incubation without inhibition of cell proliferation. Calcitriol 0-24 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 9302649-7 1997 1,25-Dihydroxyvitamin D3 and 22-oxacalcitriol inhibited cytokine-stimulated IL-8 production dose dependently after 24 h incubation without inhibition of cell proliferation. maxacalcitol 29-45 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 9302649-8 1997 1,25-Dihydroxyvitamin D3 and 22-oxacalcitriol are considered to inhibit the proliferation of keratinocytes directly and indirectly with inhibition of the secretion of IL-8 from keratinocytes. Calcitriol 0-24 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 9302649-8 1997 1,25-Dihydroxyvitamin D3 and 22-oxacalcitriol are considered to inhibit the proliferation of keratinocytes directly and indirectly with inhibition of the secretion of IL-8 from keratinocytes. maxacalcitol 29-45 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 9302649-9 1997 The inhibition of IL-8 secretion from keratinocytes by vitamin D3 could modulate the behaviour of immunocompetent cells infiltrating in the skin. Cholecalciferol 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 9292787-0 1997 Quercetin, a bioflavonoid, inhibits the induction of interleukin 8 and monocyte chemoattractant protein-1 expression by tumor necrosis factor-alpha in cultured human synovial cells. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 53-66 9292787-0 1997 Quercetin, a bioflavonoid, inhibits the induction of interleukin 8 and monocyte chemoattractant protein-1 expression by tumor necrosis factor-alpha in cultured human synovial cells. Flavonoids 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 53-66 9298535-11 1997 Pretreatment with L-NAME significantly enhanced the TNF-alpha (10(3) u)-induced neutrophil recruitment and human IL-8 equivalents production at 6 h, but not at 1 h of TNF-alpha administration (early phase). NG-Nitroarginine Methyl Ester 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 9400717-7 1997 In addition to a TNF-alpha-mediated pathway, there is growing evidence that some particles such as quartz and crocidolite can directly activate lung epithelial cells to release chemokines such as macrophage inflammatory protein-2, cytokine-induced neutrophil chemoattractant, and interleukin-8. Asbestos, Crocidolite 110-121 C-X-C motif chemokine ligand 8 Homo sapiens 280-293 9310121-5 1997 Furthermore, MTX caused a significant inhibition of both superoxide production induced by phorbol 12-myristate-13-acetate and chemotaxis induced by interleukin 8 in G-CSF-primed neutrophils. Methotrexate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 9292787-6 1997 RESULTS: Addition of quercetin suppressed TNF-alpha induced increase in the mRNA for IL-8 and MCP-1 in a dose dependent manner. Quercetin 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 9292787-8 1997 H2O2 mediated induction of IL-8 and MCP-1 genes was also inhibited by quercetin. Hydrogen Peroxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9292787-8 1997 H2O2 mediated induction of IL-8 and MCP-1 genes was also inhibited by quercetin. Quercetin 70-79 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9292787-10 1997 CONCLUSION: Quercetin suppresses TNF-alpha mediated stimulation of IL-8 and MCP-1 expression, at least in part, by inhibiting the activation of NF-kappa B. Quercetin 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 9271387-0 1997 Identification of tumor-specific paclitaxel (Taxol)-responsive regulatory elements in the interleukin-8 promoter. Paclitaxel 45-50 C-X-C motif chemokine ligand 8 Homo sapiens 90-103 9271387-3 1997 Previously, we demonstrated that paclitaxel can induce interleukin-8 (IL-8) gene expression at the transcriptional level in subsets of human ovarian cancer lines. Paclitaxel 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 9271387-3 1997 Previously, we demonstrated that paclitaxel can induce interleukin-8 (IL-8) gene expression at the transcriptional level in subsets of human ovarian cancer lines. Paclitaxel 33-43 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 9271387-6 1997 Paclitaxel only activated the IL-8 promoter in responsive cells. Paclitaxel 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 9271387-7 1997 The AP-1 and NF-kappaB binding sites in the IL-8 promoter are required for activation by paclitaxel; in contrast, a C/EBP site required for IL-8 promoter activation in other cell types is not involved. Paclitaxel 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 9271387-10 1997 These results demonstrate a molecular mechanism for cell-specific paclitaxel-induced IL-8 gene expression which may have clinical relevance. Paclitaxel 66-76 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 9267955-0 1997 Effect of ciprofloxacin on the accumulation of interleukin-6, interleukin-8, and nitrite from a human endothelial cell model of sepsis. Ciprofloxacin 10-23 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 9279218-5 1997 In BW, exposure to NO2 induced a 1.5-fold increase in interleukin-8 (IL-8) (p < 0.05) at 1.5 h and a 2.5-fold increase in neutrophils (p < 0.01) at 6 h. In BAL fluid (BALF), small increases were observed in CD45RO+ lymphocytes, B-cells, and natural killer (NK) cells only. Nitrogen Dioxide 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 9279218-5 1997 In BW, exposure to NO2 induced a 1.5-fold increase in interleukin-8 (IL-8) (p < 0.05) at 1.5 h and a 2.5-fold increase in neutrophils (p < 0.01) at 6 h. In BAL fluid (BALF), small increases were observed in CD45RO+ lymphocytes, B-cells, and natural killer (NK) cells only. Nitrogen Dioxide 19-22 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 9245487-3 1997 In the present study, using FITC-IL-8 conjugate as a probe, we have demonstrated the time- and temperature-dependent endocytosis of IL-8 under fluorescent microscope. Fluorescein-5-isothiocyanate 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 9245487-3 1997 In the present study, using FITC-IL-8 conjugate as a probe, we have demonstrated the time- and temperature-dependent endocytosis of IL-8 under fluorescent microscope. Fluorescein-5-isothiocyanate 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 9267955-8 1997 Interleukin-8 was decreased at lower ciprofloxacin concentrations (p = .017) but was increased at 100 microg/mL (p = .0039). Ciprofloxacin 37-50 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9245487-5 1997 Monodansyl cadaverine (MDC, 900 microM), however, was found to retain the fluorescent light of FITC coupled with Il-8 on the cells. monodansylcadaverine 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 9245487-5 1997 Monodansyl cadaverine (MDC, 900 microM), however, was found to retain the fluorescent light of FITC coupled with Il-8 on the cells. monodansylcadaverine 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 9267955-10 1997 CONCLUSIONS: Ciprofloxacin differentially modulates interleukin-6 and interleukin-8 expression. Ciprofloxacin 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 9245487-7 1997 With respect to control, IL-8 induced biological responses e.g. IL-8 directed migration, intracellular Ca2+ release and superoxide release are significantly reduced by 77%, 94% and 76%, respectively, in presence of MDC. Superoxides 120-130 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 9293391-0 1997 Differential modulation of IL-8 and TNF-alpha expression in human keratinocytes by buflomedil chlorhydrate and pentoxifylline. buflomedil chlorhydrate 83-106 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9293391-0 1997 Differential modulation of IL-8 and TNF-alpha expression in human keratinocytes by buflomedil chlorhydrate and pentoxifylline. Pentoxifylline 111-125 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9293391-7 1997 TPA-induced TNF-alpha and IL-8 release from keratinocytes. Tetradecanoylphorbol Acetate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 9293391-9 1997 TPA increased RNA expression of the TNF-alpha, IL-1 alpha, IL-1 beta, IL-8 and TGF-beta 1. Tetradecanoylphorbol Acetate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 9293391-10 1997 BC diminished TPA-induced TNF-alpha and IL-8 release from keratinocytes; in the case of IL-8 it is possible that this inhibition occur to transcriptional level. Tetradecanoylphorbol Acetate 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 9233596-3 1997 By introducing the N-terminal mutation delta1-5,ELR>AAR into CINC, we have developed a rat alpha-chemokine receptor antagonist (ra) analogous to a previously described mutant of human IL-8. Zinc 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 9258252-1 1997 Interleukin-8 (IL-8) is an important cytokine in inflammatory processes by functioning as a chemoattractant and as an activator of oxygen metabolism. Oxygen 131-137 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9258252-1 1997 Interleukin-8 (IL-8) is an important cytokine in inflammatory processes by functioning as a chemoattractant and as an activator of oxygen metabolism. Oxygen 131-137 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 9258252-6 1997 The effect of the beta 2-adrenergic agonist on IL-8 production is presumably mediated via increased cAMP formation, since it can be mimicked by the cAMP analogue dibutyryl-cAMP (db-cAMP). Cyclic AMP 100-104 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9258252-6 1997 The effect of the beta 2-adrenergic agonist on IL-8 production is presumably mediated via increased cAMP formation, since it can be mimicked by the cAMP analogue dibutyryl-cAMP (db-cAMP). Cyclic AMP 148-152 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9258252-6 1997 The effect of the beta 2-adrenergic agonist on IL-8 production is presumably mediated via increased cAMP formation, since it can be mimicked by the cAMP analogue dibutyryl-cAMP (db-cAMP). Bucladesine 162-176 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9258252-6 1997 The effect of the beta 2-adrenergic agonist on IL-8 production is presumably mediated via increased cAMP formation, since it can be mimicked by the cAMP analogue dibutyryl-cAMP (db-cAMP). Bucladesine 178-185 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9258252-7 1997 We conclude that enhancement of IL-8 production is one of the pathways via which beta 2-adrenergic agonists such as catecholamines can influence inflammatory responses. Catecholamines 116-130 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 9236347-6 1997 The tepid group showed an earlier decrease in interleukin-8 and neutrophil elastase levels as compared with the hypothermic group. tepid 4-9 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 9263137-3 1997 RESULTS: In MNC and synovial fibroblast cultures dexamethasone, GSTM, and PGE2 most markedly downregulated spontaneous and/or cytokine stimulated production of IL-1 beta, IL-14a, IL-8, and MCP-1, whereas sTNFR shedding was not affected. Dexamethasone 49-62 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 20654323-4 1997 The unsaturated fatty acids increased both TEWL and LDV and elevated IL-1alpha and IL-8 mRNA levels, whereas their effects on protein levels were minimal. Fatty Acids, Unsaturated 4-27 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 9253958-2 1997 Anandamide was shown to diminish interleukin-6 and interleukin-8 production at low nanomolar concentrations (3-30 nM) but inhibited the production of TNF-alpha, interferon-gamma, interleukin-4 and p75 TNF-alpha soluble receptors at higher concentrations (0.3-3 microM). anandamide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 9253958-3 1997 Palmitoylethanolamide inhibited interleukin-4, interleukin-6, interleukin-8 synthesis and the production of p75 TNF-alpha soluble receptors at concentrations similar to those of anandamide but failed to influence TNF-alpha and interferon-gamma production. palmidrol 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 9228216-6 1997 The immunoreactivity of markers for epidermal proliferation and differentiation, as well as of CD1a and NAP-1/IL-8, changed after 8 weeks of calcitriol treatment almost completely to the pattern characteristic for non-lesional psoriatic skin, while a large number of 55 kDa TNF-receptor positive cells could be found in the dermal compartment. Calcitriol 141-151 C-X-C motif chemokine ligand 8 Homo sapiens 104-109 9228216-6 1997 The immunoreactivity of markers for epidermal proliferation and differentiation, as well as of CD1a and NAP-1/IL-8, changed after 8 weeks of calcitriol treatment almost completely to the pattern characteristic for non-lesional psoriatic skin, while a large number of 55 kDa TNF-receptor positive cells could be found in the dermal compartment. Calcitriol 141-151 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 9263137-3 1997 RESULTS: In MNC and synovial fibroblast cultures dexamethasone, GSTM, and PGE2 most markedly downregulated spontaneous and/or cytokine stimulated production of IL-1 beta, IL-14a, IL-8, and MCP-1, whereas sTNFR shedding was not affected. Gold Sodium Thiomalate 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 9263137-3 1997 RESULTS: In MNC and synovial fibroblast cultures dexamethasone, GSTM, and PGE2 most markedly downregulated spontaneous and/or cytokine stimulated production of IL-1 beta, IL-14a, IL-8, and MCP-1, whereas sTNFR shedding was not affected. Dinoprostone 74-78 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 9253958-7 1997 TNF-alpha, interleukin-6 and interleukin-8 synthesis was maximally inhibited by 3 nM delta9-tetrahydrocannabinol but stimulated by 3 microM delta9-tetrahydrocannabinol, as was interleukin-8 and interferon-gamma synthesis. Dronabinol 85-112 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 9253958-7 1997 TNF-alpha, interleukin-6 and interleukin-8 synthesis was maximally inhibited by 3 nM delta9-tetrahydrocannabinol but stimulated by 3 microM delta9-tetrahydrocannabinol, as was interleukin-8 and interferon-gamma synthesis. Dronabinol 140-167 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 9230759-0 1997 Erythromycin modulates IL-8 expression in normal and inflamed human bronchial epithelial cells. Erythromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 9230759-4 1997 EM and clarithromycin (CAM) uniquely suppressed mRNA levels as well as the release of IL-8 at the therapeutic and noncytotoxic concentrations (% inhibition of IL-8 protein release: 25.0 +/- 5.67% and 37.5 +/- 8.99%, respectively, at 10(-6) M). Erythromycin 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 9230759-4 1997 EM and clarithromycin (CAM) uniquely suppressed mRNA levels as well as the release of IL-8 at the therapeutic and noncytotoxic concentrations (% inhibition of IL-8 protein release: 25.0 +/- 5.67% and 37.5 +/- 8.99%, respectively, at 10(-6) M). Clarithromycin 7-21 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 9230759-4 1997 EM and clarithromycin (CAM) uniquely suppressed mRNA levels as well as the release of IL-8 at the therapeutic and noncytotoxic concentrations (% inhibition of IL-8 protein release: 25.0 +/- 5.67% and 37.5 +/- 8.99%, respectively, at 10(-6) M). Clarithromycin 7-21 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 9230759-4 1997 EM and clarithromycin (CAM) uniquely suppressed mRNA levels as well as the release of IL-8 at the therapeutic and noncytotoxic concentrations (% inhibition of IL-8 protein release: 25.0 +/- 5.67% and 37.5 +/- 8.99%, respectively, at 10(-6) M). Clarithromycin 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 9230759-7 1997 Among five patients who underwent bronchoscopy before and after macrolide treatment, four showed decreased levels of IL-8 expression in airway epithelium as assessed by reverse transcription and polymerase chain reaction. Macrolides 64-73 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 9266021-0 1997 The demonstration of serum interleukin-8 and superoxide dismutase in Adamantiades-Behcet"s disease. adamantiades 69-81 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 9268748-8 1997 Preincubation on normal neutrophils with the patients" sera caused an increase in their superoxide generation in accordance with the high IL-8 levels in these sera. Superoxides 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 19856299-1 1997 This study demonstrates the changing levels of leukotrieneB4 (LTB4) and leukotrieneC4 (LTC4) generated by human white blood cells primed with different human interleukins IL-3, IL-5, IL-6, IL-8 and with human hematopoietic growth factor granulocyte-macrophage colony stimulating factor (GM-CSF). Leukotriene B4 47-60 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 19856299-1 1997 This study demonstrates the changing levels of leukotrieneB4 (LTB4) and leukotrieneC4 (LTC4) generated by human white blood cells primed with different human interleukins IL-3, IL-5, IL-6, IL-8 and with human hematopoietic growth factor granulocyte-macrophage colony stimulating factor (GM-CSF). Leukotriene C4 72-85 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 9240177-1 1997 OBJECTIVE: To determine the effects of isoniazid (isonicotinic acid hydrazide), used to reduce the serious side-effects of immunotherapy of superficial bladder cancer with bacille Calmette-Guerin (BCG), on the proliferation and constitutive BCG-induced synthesis of interleukins 6 (IL6) and 8 (IL8) in human bladder cancer cells cultured in vitro. Isoniazid 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 294-297 9240177-1 1997 OBJECTIVE: To determine the effects of isoniazid (isonicotinic acid hydrazide), used to reduce the serious side-effects of immunotherapy of superficial bladder cancer with bacille Calmette-Guerin (BCG), on the proliferation and constitutive BCG-induced synthesis of interleukins 6 (IL6) and 8 (IL8) in human bladder cancer cells cultured in vitro. Isoniazid 50-77 C-X-C motif chemokine ligand 8 Homo sapiens 294-297 9284961-1 1997 Relatively high concentrations of azathioprine had an inhibitory effect on interleukin 8 (IL-8)- or formyl-methionyl-leucyl-phenylalanine-activated (fMLP)-chemotaxis by human neutrophils. Azathioprine 34-46 C-X-C motif chemokine ligand 8 Homo sapiens 75-88 9284961-1 1997 Relatively high concentrations of azathioprine had an inhibitory effect on interleukin 8 (IL-8)- or formyl-methionyl-leucyl-phenylalanine-activated (fMLP)-chemotaxis by human neutrophils. Azathioprine 34-46 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 9284961-6 1997 High concentrations of azathioprine (1 mM) inhibited CD11b expression of fMLP- or IL-8- activated neutrophils; the latter could explain the inhibitory effect of azathioprine. Azathioprine 23-35 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 9284961-6 1997 High concentrations of azathioprine (1 mM) inhibited CD11b expression of fMLP- or IL-8- activated neutrophils; the latter could explain the inhibitory effect of azathioprine. Azathioprine 161-173 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 9284961-9 1997 The antagonists had only a marginal effect on inhibition of IL-8-activated chemotaxis by high concentrations of azathioprine, thus the G-kinase seems not to be of great importance on the inhibitory effect of azathioprine. Azathioprine 112-124 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9237814-1 1997 The aim of this study was to investigate the roles of protein kinase A (PKA), protein kinase C (PKC), protein tyrosine kinase (PTK) and intracellular calcium in the induction of IL-8 production by gastric epithelial cells. Calcium 150-157 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 9237814-6 1997 Activation of PKC by phorbol myristate acetate was also an effective stimulus to IL-8 production and this was blocked by PKC depletion or inhibitors. Tetradecanoylphorbol Acetate 21-46 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 9237814-9 1997 The calcium ionophore A23187 was a weak, PKC dependent, stimulant of IL-8 production. Calcium 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 9237814-9 1997 The calcium ionophore A23187 was a weak, PKC dependent, stimulant of IL-8 production. Calcimycin 22-28 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 9223588-0 1997 The natural product hymenialdisine inhibits interleukin-8 production in U937 cells by inhibition of nuclear factor-kappaB. hymenialdisine 20-34 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 9212819-5 1997 In this way, we were able to detect IL-8 with a monoclonal antibody in stimulated cells that were microwave-fixed with a combination of paraformaldehyde (4%) and glutaraldehyde (0.1%), followed by permeabilization with saponin (0.025%). paraform 136-152 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 9212819-5 1997 In this way, we were able to detect IL-8 with a monoclonal antibody in stimulated cells that were microwave-fixed with a combination of paraformaldehyde (4%) and glutaraldehyde (0.1%), followed by permeabilization with saponin (0.025%). Glutaral 162-176 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 9212819-5 1997 In this way, we were able to detect IL-8 with a monoclonal antibody in stimulated cells that were microwave-fixed with a combination of paraformaldehyde (4%) and glutaraldehyde (0.1%), followed by permeabilization with saponin (0.025%). Saponins 219-226 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 9223588-8 1997 Functional studies showed hymenialdisine to be an inhibitor of IL-8 production and IL-8 mRNA formation in the U937 cell. hymenialdisine 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 9223588-8 1997 Functional studies showed hymenialdisine to be an inhibitor of IL-8 production and IL-8 mRNA formation in the U937 cell. hymenialdisine 26-40 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 9223588-11 1997 Thus, hymenialdisine is a potent inhibitor of NF-kappaB and IL-8 production in U937 cells. hymenialdisine 6-20 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9507569-7 1997 Exposure of cyclosporin A and dexamethasone almost completely inhibited the production of IL-6 and IL-8 after 24 hours of treatment. Cyclosporine 12-25 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 9252959-10 1997 ET-18-OCH3 uptake in the HL-60 cell line was also more sensitive to treatment with endocytic (chloroquine, monensin) or metabolic (NaF, KCN) inhibitors. et-18 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 9252959-10 1997 ET-18-OCH3 uptake in the HL-60 cell line was also more sensitive to treatment with endocytic (chloroquine, monensin) or metabolic (NaF, KCN) inhibitors. och3 6-10 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 9199336-7 1997 Administration of a NF-kappaB antisense oligonucleotide almost completely inhibited TNF-alpha-dependent IL-8 production and partially abrogated TNF-alpha-dependent VEGF production, and an Sp1 antisense sequence partially inhibited TNF-alpha-dependent production of VEGF. Oligonucleotides 40-55 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 9507569-7 1997 Exposure of cyclosporin A and dexamethasone almost completely inhibited the production of IL-6 and IL-8 after 24 hours of treatment. Dexamethasone 30-43 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 9182566-0 1997 Stimulation of interleukin-8 production by okadaic acid and vanadate in a human promyelocyte cell line, an HL-60 subline. Okadaic Acid 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 9182566-0 1997 Stimulation of interleukin-8 production by okadaic acid and vanadate in a human promyelocyte cell line, an HL-60 subline. Vanadates 60-68 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 9182566-7 1997 IL-8 production by OA or VA was inhibited by protein kinase inhibitors, including staurosporine, H-7, K252a, herbimycin A, and genistein. Vanillic Acid 25-27 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9182566-7 1997 IL-8 production by OA or VA was inhibited by protein kinase inhibitors, including staurosporine, H-7, K252a, herbimycin A, and genistein. Staurosporine 82-95 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9182566-7 1997 IL-8 production by OA or VA was inhibited by protein kinase inhibitors, including staurosporine, H-7, K252a, herbimycin A, and genistein. 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9182566-7 1997 IL-8 production by OA or VA was inhibited by protein kinase inhibitors, including staurosporine, H-7, K252a, herbimycin A, and genistein. staurosporine aglycone 102-107 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9182566-7 1997 IL-8 production by OA or VA was inhibited by protein kinase inhibitors, including staurosporine, H-7, K252a, herbimycin A, and genistein. herbimycin 109-121 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9182566-7 1997 IL-8 production by OA or VA was inhibited by protein kinase inhibitors, including staurosporine, H-7, K252a, herbimycin A, and genistein. Genistein 127-136 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9176395-9 1997 Preincubation of HUVECs with pyrrolidine dithiocarbamate prevented MAC-induced increases in IL-8 and MCP-1 mRNA concentrations and protein secretion. pyrrolidine dithiocarbamic acid 29-56 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 9215025-9 1997 Nitric oxide and superoxide have profound effects on IL-8. Superoxides 17-27 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9227164-1 1997 OBJECTIVE: To investigate whether administration of sodium fluoride (NaF) in addition to cyclical etidronate has a positive effect on bone mineral density (BMD) in patients with established osteoporosis during continued treatment with corticosteroids. Sodium Fluoride 52-67 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 9227164-7 1997 RESULTS: After two years of treatment, the BMD of the lumbar spine in the etidronate/NaF group had increased by +9.3% (95% confidence intervals (CI): +2.3% to +16.2%, p < 0.01), while the BMD in the etidronate/placebo group was unchanged: +0.3% (95% CI: -2.2% to +2.8%). Etidronic Acid 202-212 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 9227164-12 1997 CONCLUSION: The effect of combination treatment with NaF and etidronate on the BMD of the lumbar spine in corticosteroid treated patients with established osteoporosis is superior to that of etidronate alone. Etidronic Acid 191-201 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 9215025-0 1997 Effect of exogenous nitric oxide and superoxide on interleukin-8 from human polymorphonuclear leucocytes. Nitric Oxide 20-32 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 9192939-7 1997 In contrast, DTT-treated sputum had higher total cell counts (median 8.8 vs 2.8 x 10(6) mL(-1); p<0.001) and levels of ECP (median 1340 vs 584 mg x L(-1); p<0.001) The measurements were similar with respect to the proportion of eosinophils, neutrophils, lymphocytes, macrophages, and fluid-phase fibrinogen, IL-5 and IL-8. Dithiothreitol 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 323-327 9215025-0 1997 Effect of exogenous nitric oxide and superoxide on interleukin-8 from human polymorphonuclear leucocytes. Superoxides 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 9215025-6 1997 The combined nitric oxide-superoxide donor, 3-morpholinosydnonimine (SIN-1), dose-dependently decreased lipopolysaccharide-mediated IL-8 accumulation (P < 0.01). nitric oxide-superoxide 13-36 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 9215025-6 1997 The combined nitric oxide-superoxide donor, 3-morpholinosydnonimine (SIN-1), dose-dependently decreased lipopolysaccharide-mediated IL-8 accumulation (P < 0.01). linsidomine 44-67 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 9215025-8 1997 In contrast, the pure nitric oxide donor, 1,2,3,4-oxatriazolium 5-amino chloride (GEA-3162), increased stimulated IL-8 accumulation (P < 0.01) and also increased IL-8 accumulation in unstimulated cells (P < 0.002). Nitric Oxide 22-34 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 9215025-8 1997 In contrast, the pure nitric oxide donor, 1,2,3,4-oxatriazolium 5-amino chloride (GEA-3162), increased stimulated IL-8 accumulation (P < 0.01) and also increased IL-8 accumulation in unstimulated cells (P < 0.002). Nitric Oxide 22-34 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 9215025-8 1997 In contrast, the pure nitric oxide donor, 1,2,3,4-oxatriazolium 5-amino chloride (GEA-3162), increased stimulated IL-8 accumulation (P < 0.01) and also increased IL-8 accumulation in unstimulated cells (P < 0.002). 1,2,3,4-oxatriazolium 5-amino chloride 42-80 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 9215025-8 1997 In contrast, the pure nitric oxide donor, 1,2,3,4-oxatriazolium 5-amino chloride (GEA-3162), increased stimulated IL-8 accumulation (P < 0.01) and also increased IL-8 accumulation in unstimulated cells (P < 0.002). 1,2,3,4-oxatriazolium 5-amino chloride 42-80 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 9215025-8 1997 In contrast, the pure nitric oxide donor, 1,2,3,4-oxatriazolium 5-amino chloride (GEA-3162), increased stimulated IL-8 accumulation (P < 0.01) and also increased IL-8 accumulation in unstimulated cells (P < 0.002). gea 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 9215025-8 1997 In contrast, the pure nitric oxide donor, 1,2,3,4-oxatriazolium 5-amino chloride (GEA-3162), increased stimulated IL-8 accumulation (P < 0.01) and also increased IL-8 accumulation in unstimulated cells (P < 0.002). gea 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 9215025-9 1997 Nitric oxide and superoxide have profound effects on IL-8. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9225534-1 1997 OBJECTIVE: The study was designed to test the hypothesis that a dentifrice with fluoride at the same concentration (1000ppm) from two sources, ie NaF and NaMFP, would provide a greater treatment effect than one with NaMFP alone. Fluorides 80-88 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 9169777-0 1997 Lipopolysaccharide-induced interleukin 8 production by human whole blood is enhanced by epinephrine and inhibited by hydrocortisone. Epinephrine 88-99 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 9437256-3 1997 The antioxidant effect of NAF was about 3 times less potent than that of alpha-tocopherol (alpha-TOC) in phosphatidylcholine liposomes, and NAF was about 2-4 times more efficient to decrease peroxidation of LDL than alpha-TOC. Phosphatidylcholines 105-124 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 9437256-4 1997 Possible interaction of NAF with alpha-tocopherol radical (alpha-TR) was studied by EPR spectroscopy. alpha-tocopherol radical 33-57 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 9222021-5 1997 Locally acting prostaglandins modulate vascular permeability, and a synergistic action of prostaglandin E (PGE) with IL-8 has been described. Prostaglandins E 90-105 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 9222021-5 1997 Locally acting prostaglandins modulate vascular permeability, and a synergistic action of prostaglandin E (PGE) with IL-8 has been described. Prostaglandins E 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 9169777-0 1997 Lipopolysaccharide-induced interleukin 8 production by human whole blood is enhanced by epinephrine and inhibited by hydrocortisone. Hydrocortisone 117-131 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 9169777-2 1997 Epinephrine caused a dose-dependent increase in LPS-induced IL-8 production, which was mediated exclusively via beta-adrenergic receptors, as reflected by the facts that beta (but not alpha) receptor blockade reversed the epinephrine effect and beta (but not alpha) receptor stimulation reproduced the epinephrine effect. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9169777-2 1997 Epinephrine caused a dose-dependent increase in LPS-induced IL-8 production, which was mediated exclusively via beta-adrenergic receptors, as reflected by the facts that beta (but not alpha) receptor blockade reversed the epinephrine effect and beta (but not alpha) receptor stimulation reproduced the epinephrine effect. Epinephrine 222-233 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9169777-2 1997 Epinephrine caused a dose-dependent increase in LPS-induced IL-8 production, which was mediated exclusively via beta-adrenergic receptors, as reflected by the facts that beta (but not alpha) receptor blockade reversed the epinephrine effect and beta (but not alpha) receptor stimulation reproduced the epinephrine effect. Epinephrine 302-313 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9169777-3 1997 Further, elevating cellular cyclic AMP (cAMP) concentrations, a known effect of beta-adrenergic stimulation, by addition of dibutyryl cAMP also enhanced LPS-induced IL-8 production. Cyclic AMP 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 9169777-3 1997 Further, elevating cellular cyclic AMP (cAMP) concentrations, a known effect of beta-adrenergic stimulation, by addition of dibutyryl cAMP also enhanced LPS-induced IL-8 production. Cyclic AMP 40-44 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 9169777-3 1997 Further, elevating cellular cyclic AMP (cAMP) concentrations, a known effect of beta-adrenergic stimulation, by addition of dibutyryl cAMP also enhanced LPS-induced IL-8 production. Cyclic AMP 134-138 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 9169777-4 1997 Epinephrine-induced upregulation of IL-10 production masked an even more pronounced stimulating effect of this hormone on IL-8 synthesis, as indicated by the finding that the extent of IL-8 upregulation was greater in the presence of anti-IL-10 than in the absence of anti-IL-10. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 9169777-4 1997 Epinephrine-induced upregulation of IL-10 production masked an even more pronounced stimulating effect of this hormone on IL-8 synthesis, as indicated by the finding that the extent of IL-8 upregulation was greater in the presence of anti-IL-10 than in the absence of anti-IL-10. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 9169777-5 1997 Hydrocortisone dose-dependently inhibited LPS-induced IL-8 production and reversed epinephrine-induced enhancement of IL-8 production. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9169777-5 1997 Hydrocortisone dose-dependently inhibited LPS-induced IL-8 production and reversed epinephrine-induced enhancement of IL-8 production. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 9169777-5 1997 Hydrocortisone dose-dependently inhibited LPS-induced IL-8 production and reversed epinephrine-induced enhancement of IL-8 production. Epinephrine 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 9169777-6 1997 Epinephrine and hydrocortisone have opposite effects on IL-8 production, which may be relevant for the understanding of endogenous and therapeutic stress hormone influences on IL-8 mediated inflammation. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 9169777-6 1997 Epinephrine and hydrocortisone have opposite effects on IL-8 production, which may be relevant for the understanding of endogenous and therapeutic stress hormone influences on IL-8 mediated inflammation. Epinephrine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 9169777-6 1997 Epinephrine and hydrocortisone have opposite effects on IL-8 production, which may be relevant for the understanding of endogenous and therapeutic stress hormone influences on IL-8 mediated inflammation. Hydrocortisone 16-30 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 9169777-6 1997 Epinephrine and hydrocortisone have opposite effects on IL-8 production, which may be relevant for the understanding of endogenous and therapeutic stress hormone influences on IL-8 mediated inflammation. Hydrocortisone 16-30 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 9151824-6 1997 Although M-T7 retains binding to a number of interleukin-8 N-terminal (ELR) deletion mutants, binding to mutants containing deletions in the C-terminal heparin-binding domain of interleukin-8 is abrogated. Heparin 152-159 C-X-C motif chemokine ligand 8 Homo sapiens 178-191 9201300-6 1997 IL-8 mRNA expressed by HT-29 cells in response to E. histolytica trophozoites was downregulated in the presence of galactose, N-acetylgalactosamine or N-acetyl-lactosamine (0.1-100 mM), and this was paralleled by decreased IL-8 protein secretion. Galactose 115-124 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9217378-0 1997 [Effects of pre-operative administration of steroids on the serum interleukin (IL)-6, IL-8 and organ injuries in replacement of thoracic aorta]. Steroids 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 9217378-1 1997 To investigate whether pre-operative steroids administration decreases the post-operative serum IL-6, IL-8 and prevents organ injuries, we prospectively studied patients undergoing elective replacement of thoracic aorta using an extracorporeal circulation. Steroids 37-45 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 9217378-4 1997 These findings show that in replacement of thoracic aorta, pre-operative steroid administration decreases the post-operative elevations of serum inflammatory cytokines (IL-6 and IL-8) and may prevent organ injuries. Steroids 73-80 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 9201300-6 1997 IL-8 mRNA expressed by HT-29 cells in response to E. histolytica trophozoites was downregulated in the presence of galactose, N-acetylgalactosamine or N-acetyl-lactosamine (0.1-100 mM), and this was paralleled by decreased IL-8 protein secretion. Acetylgalactosamine 126-147 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9261930-0 1997 Effects of long-term low-dose macrolide administration on neutrophil recruitment and IL-8 in the nasal discharge of chronic sinusitis patients. Macrolides 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 9261930-6 1997 These findings suggest that long-term low-dose roxithromycin administration inhibits the positive feedback mechanism of neutrophil recruitment and IL-8 production by the recruited neutrophils, which is considered to be an essential cause of the prolongation of sinusitis. Roxithromycin 47-60 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 9201300-6 1997 IL-8 mRNA expressed by HT-29 cells in response to E. histolytica trophozoites was downregulated in the presence of galactose, N-acetylgalactosamine or N-acetyl-lactosamine (0.1-100 mM), and this was paralleled by decreased IL-8 protein secretion. N-acetyllactosamine 151-171 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9201300-6 1997 IL-8 mRNA expressed by HT-29 cells in response to E. histolytica trophozoites was downregulated in the presence of galactose, N-acetylgalactosamine or N-acetyl-lactosamine (0.1-100 mM), and this was paralleled by decreased IL-8 protein secretion. N-acetyllactosamine 151-171 C-X-C motif chemokine ligand 8 Homo sapiens 223-227 9154890-6 1997 Two major volatile factors in cigarette smoke, acrolein and acetaldehyde, augmented IL-8 release. Acrolein 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9154890-6 1997 Two major volatile factors in cigarette smoke, acrolein and acetaldehyde, augmented IL-8 release. Acetaldehyde 60-72 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9145235-2 1997 In clinical trials, both treatments increase bone density, although sodium fluoride (NaF) increases and alendronate (bisphosphonate, ALN) decreases bone turnover. Sodium Fluoride 68-83 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 9165232-0 1997 High glucose enhances the gene expression of interleukin-8 in human endothelial cells, but not in smooth muscle cells: possible role of interleukin-8 in diabetic macroangiopathy. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 45-58 9181275-4 1997 Among the serum cytokines mainly produced by monocytes/macrophages interleukin (IL)-8 levels were decreased in steroid-sensitive patients vs controls, with normal levels observed for IL-1 alpha, IL-1 beta, IL-1RA and tumor necrosis factor (TNF-alpha). Steroids 111-118 C-X-C motif chemokine ligand 8 Homo sapiens 67-85 9165232-1 1997 We examined the effect of high glucose concentrations on the production of interleukin(IL)-8, which seems to be important for the development of atherosclerosis, in cultured human aortic endothelial cells (AoEC) and smooth muscle cells (AoSMC). Glucose 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 75-92 9165232-3 1997 After 2 days" culture, 42.5 mmol/l glucose enhanced IL-8 mRNA expression in AoEC, but not in AoSMC, compared to 4 mmol/l glucose. Glucose 35-42 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 9179547-1 1997 Superoxide release in neutrophils and sera levels of interleukin 8 (IL-8) were determined in 15 patients with complicated acute myocardial infarction (MI) and 15 patients with uncomplicated MI. Superoxides 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 9165232-4 1997 After 7 days" culture, the IL-8 concentration in AoEC lysate and the expression of IL-8 mRNA were significantly increased by 20.5 mmol/l glucose, or 42.5 mmol/l glucose compared to 4 mmol/l glucose. Glucose 137-144 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9165232-4 1997 After 7 days" culture, the IL-8 concentration in AoEC lysate and the expression of IL-8 mRNA were significantly increased by 20.5 mmol/l glucose, or 42.5 mmol/l glucose compared to 4 mmol/l glucose. Glucose 137-144 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 9165232-4 1997 After 7 days" culture, the IL-8 concentration in AoEC lysate and the expression of IL-8 mRNA were significantly increased by 20.5 mmol/l glucose, or 42.5 mmol/l glucose compared to 4 mmol/l glucose. Glucose 161-168 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9165232-4 1997 After 7 days" culture, the IL-8 concentration in AoEC lysate and the expression of IL-8 mRNA were significantly increased by 20.5 mmol/l glucose, or 42.5 mmol/l glucose compared to 4 mmol/l glucose. Glucose 161-168 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 9165232-4 1997 After 7 days" culture, the IL-8 concentration in AoEC lysate and the expression of IL-8 mRNA were significantly increased by 20.5 mmol/l glucose, or 42.5 mmol/l glucose compared to 4 mmol/l glucose. Glucose 161-168 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 9136832-8 1997 Cycloheximide treatment resulted in superinduction of IL-8 mRNA; however, dexamethasone inhibited E. histolytica-induced IL-8 gene expression. Cycloheximide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 9165232-4 1997 After 7 days" culture, the IL-8 concentration in AoEC lysate and the expression of IL-8 mRNA were significantly increased by 20.5 mmol/l glucose, or 42.5 mmol/l glucose compared to 4 mmol/l glucose. Glucose 161-168 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 9136832-8 1997 Cycloheximide treatment resulted in superinduction of IL-8 mRNA; however, dexamethasone inhibited E. histolytica-induced IL-8 gene expression. Dexamethasone 74-87 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 9165232-5 1997 On the other hand, the IL-8 concentration in AoSMC lysate was not affected by any glucose concentration and the expression of IL-8 mRNA in AoSMC was diminished by high glucose. Glucose 168-175 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 9165232-6 1997 These results suggest that the chemotactic gradient by IL-8 is established between arterial intima and media in response to high glucose levels in diabetic patients, and that it may be one of the key factors for SMC migration to the intima leading to diabetic macroangiopathy. Glucose 129-136 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 9136936-4 1997 Using an immunostaining method that enables simultaneous detection of cytokines and phenotype, 56 +/- 6% CD34+ peripheral blood progenitor cells (PBPC) were found to contain cytoplasmic IL-8 after stimulation with phorbol myristate acetate + ionomycin for 90 min. Tetradecanoylphorbol Acetate 214-239 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 9188199-0 1997 Production of human interleukin-8 expressed in Escherichia coli: from a laboratory scale for in vitro tests via a technical scale for animal studies to a process scale for a GMP-compatible production. guanosine 5'-monophosphorothioate 174-177 C-X-C motif chemokine ligand 8 Homo sapiens 20-33 9130647-0 1997 Chemoattractant receptors for interleukin-8 and C5a: expression on peripheral blood leukocytes and differential regulation on HL-60 and AML-193 cells by vitamin D3 and all-trans retinoic acid. Cholecalciferol 153-163 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 9130647-0 1997 Chemoattractant receptors for interleukin-8 and C5a: expression on peripheral blood leukocytes and differential regulation on HL-60 and AML-193 cells by vitamin D3 and all-trans retinoic acid. Tretinoin 178-191 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 9161853-2 1997 We measured creatinine-collected urinary levels of IL-6 and IL-8 by an enzyme-linked immunosorbent assay in 21 women with urethritis syndrome as well as 20 age-matched healthy women. Creatinine 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 9176105-8 1997 AcLDL stimulated IL-8 secretion > TNF-alpha > IL-1 alpha > IL-2 = IFN-gamma = IL-1 beta, and decreased GM-CSF secretion eightfold. acldl 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 9170624-2 1997 Radioiodination of IL-8 was catalysed by chloramine-T, and human leukocytes were radiolabelled with 111In-oxine. chloramine-T 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 9170624-2 1997 Radioiodination of IL-8 was catalysed by chloramine-T, and human leukocytes were radiolabelled with 111In-oxine. indium oxine 100-111 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 9096344-3 1997 We demonstrate that phosphatidylinositol-3-kinase (PI3K) activity, as determined by inhibition using wortmannin and LY294002, is required for IL-8-induced cell migration of human neutrophils. Wortmannin 101-111 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 9155955-0 1997 Anthralin (dithranol) in vitro inhibits human monocytes to secrete IL-6, IL-8 and TNF-alpha, but not IL-1. Anthralin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 9155955-0 1997 Anthralin (dithranol) in vitro inhibits human monocytes to secrete IL-6, IL-8 and TNF-alpha, but not IL-1. Anthralin 11-20 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 9155955-9 1997 The results show a dose-dependent inhibition of MO IL-6, IL-8, and TNF-alpha release with a half-maximal inhibitory concentration of 0.25-0.6 microgram/ml of anthralin. Anthralin 158-167 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9146930-10 1997 For healthy subjects and the four patients exposed to saline, the level of IL-8 did not increase after challenge in comparison with that at baseline. Sodium Chloride 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 9096344-3 1997 We demonstrate that phosphatidylinositol-3-kinase (PI3K) activity, as determined by inhibition using wortmannin and LY294002, is required for IL-8-induced cell migration of human neutrophils. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 116-124 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 9096344-5 1997 The regulation of cell migration by IL-8 is independent of ERK kinase and ERK activation since the ERK kinase inhibitor PD098059 had no effect on IL-8-induced cell migration of human neutrophils. 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one 120-128 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 9141135-1 1997 The characteristic CXC chemokine disulfide core of interleukin-8 (IL-8) has been rearranged in a variant replacing the 9-50 disulfide with a 9-38 disulfide. Disulfides 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 9087177-4 1997 In contrast, exposure of PBMC to hyperosmotic conditions (330-410 mOsM) by the addition of NaCl to tissue culture medium induced gene expression for IL-1 alpha, IL-1 beta, and IL-8. PBMC 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 9141135-1 1997 The characteristic CXC chemokine disulfide core of interleukin-8 (IL-8) has been rearranged in a variant replacing the 9-50 disulfide with a 9-38 disulfide. Disulfides 33-42 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 9141135-1 1997 The characteristic CXC chemokine disulfide core of interleukin-8 (IL-8) has been rearranged in a variant replacing the 9-50 disulfide with a 9-38 disulfide. 9-50 disulfide 119-133 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 9141135-1 1997 The characteristic CXC chemokine disulfide core of interleukin-8 (IL-8) has been rearranged in a variant replacing the 9-50 disulfide with a 9-38 disulfide. 9-50 disulfide 119-133 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 9141135-1 1997 The characteristic CXC chemokine disulfide core of interleukin-8 (IL-8) has been rearranged in a variant replacing the 9-50 disulfide with a 9-38 disulfide. 38 disulfide 143-155 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 9141135-1 1997 The characteristic CXC chemokine disulfide core of interleukin-8 (IL-8) has been rearranged in a variant replacing the 9-50 disulfide with a 9-38 disulfide. 38 disulfide 143-155 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 9141135-5 1997 The Glu38-->Cys/Cys50-->Ala IL-8 crystallizes in space group P2(1)2(1)2(1) with cell parameters a = 46.4, b = 49.2, and c = 69.5 A, and has been refined to an R-value of 19.4% for data from 10 to 2 A resolution. Cysteine 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9141135-5 1997 The Glu38-->Cys/Cys50-->Ala IL-8 crystallizes in space group P2(1)2(1)2(1) with cell parameters a = 46.4, b = 49.2, and c = 69.5 A, and has been refined to an R-value of 19.4% for data from 10 to 2 A resolution. Alanine 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 9125224-1 1997 LPS-induced expression of the IL-8 gene was markedly enhanced by H2O2 or by deprivation of the cellular antioxidant glutathione by L-buthionine-(S,R)-sulfoximine (BSO) in human astrocytoma U373 cells. Hydrogen Peroxide 65-69 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 9125224-1 1997 LPS-induced expression of the IL-8 gene was markedly enhanced by H2O2 or by deprivation of the cellular antioxidant glutathione by L-buthionine-(S,R)-sulfoximine (BSO) in human astrocytoma U373 cells. Glutathione 116-127 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 9125224-1 1997 LPS-induced expression of the IL-8 gene was markedly enhanced by H2O2 or by deprivation of the cellular antioxidant glutathione by L-buthionine-(S,R)-sulfoximine (BSO) in human astrocytoma U373 cells. l-buthionine sulfoximine 131-161 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 9125224-1 1997 LPS-induced expression of the IL-8 gene was markedly enhanced by H2O2 or by deprivation of the cellular antioxidant glutathione by L-buthionine-(S,R)-sulfoximine (BSO) in human astrocytoma U373 cells. Buthionine Sulfoximine 163-166 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 9087177-4 1997 In contrast, exposure of PBMC to hyperosmotic conditions (330-410 mOsM) by the addition of NaCl to tissue culture medium induced gene expression for IL-1 alpha, IL-1 beta, and IL-8. Sodium Chloride 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 9125204-1 1997 Chemotactic factors, i.e., an N-formyl peptide, C5a, interleukin-8, and leukotriene B4, induced neutrophils to activate mitogen-activated protein (MAP) kinases, as defined by the tyrosine phosphorylation and decrease in electrophoretic mobility of immunodetected 44-, 42-, and 40-kDa proteins. Tyrosine 179-187 C-X-C motif chemokine ligand 8 Homo sapiens 53-66 9084925-0 1997 Effects of long-term administration of roxithromycin on neutrophil count and interleukin-8 level in endometrial cavity subjected to pyometra. Roxithromycin 39-52 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 9124593-3 1997 TNF-alpha or PAF alone induced only approximately two- to threefold increases in membrane-bound elastase but exhibited marked dose- and time-dependent priming effects for subsequent stimulation with fMLP or IL-8 (up to 20-fold increases in membrane-bound human leukocyte elastase compared with unstimulated cells). Platelet Activating Factor 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 9140523-3 1997 Although IL-5 alone induced little or no IL-8 production from eosinophils, short-term preincubation with IL-5 markedly enhanced the eosinophil IL-8 generation caused by C5a plus cytochalasin B (CB). Cytochalasin B 178-192 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 9134225-13 1997 One of the following cytokines (epidermal growth factor, transforming growth factor alpha, interleukin-1 alpha, interleukin-1 beta, interleukin-6, interleukin-8) was required for 1,25(OH)2D3 to suppress clonal growth and induce cell differentiation. 25(oh)2d3 181-190 C-X-C motif chemokine ligand 8 Homo sapiens 147-160 9135521-5 1997 All chemokines inhibited IL-8 induced chemotaxis and calcium ion mobilisation by IELs, with IL-8 having the greatest effect and MCP the least. Calcium 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 9118711-9 1997 Finally, short-term exposure to cocaine enhanced production of interleukin 8, a potent PMN chemoattractant and neutrophil-activating factor associated with both acute and chronic lung injury. Cocaine 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 9138479-5 1997 On the other hand, PGE1 significantly increased type I collagenase activity and IL-8 production in the SDF culture supernatants and it increased IL-6 and TGF-beta(1) production in both types of fibroblasts. Alprostadil 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 9108184-4 1997 Interleukin-8 release from alveolar macrophages correlated with the upregulated spontaneous luminol enhanced oxidative response of pulmonary phagocytes but not with the neutrophil count in BALF. Luminol 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9108184-6 1997 Further, a negative correlation between interleukin-8 release of alveolar macrophages and the arterial pO2 at the time of BALF could be demonstrated (r = -0.47, p < 0.05). PO-2 103-106 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 9070442-8 1997 At salt concentrations, temperatures, and pH conditions lower than physiological, the dimerization affinity of IL-8 is greatly enhanced. Salts 3-7 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 9597442-0 1997 [Il-8 secretion by cultured epithelial cells of human nasal mucosa and its suppression by macrolide antibiotics]. macrolide antibiotics 90-111 C-X-C motif chemokine ligand 8 Homo sapiens 1-5 9597446-0 1997 [Effects of a steroid and macrolide antibiotic on IL-8 production by neutrophils]. Steroids 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 9597446-0 1997 [Effects of a steroid and macrolide antibiotic on IL-8 production by neutrophils]. Macrolides 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 9071565-4 1997 Serum nitrate levels correlated significantly with both pro-inflammatory cytokines (IL-6, IL-8, TNF-alpha) as well as anti-inflammatory cytokines (IL-10, TNFsrI, TNFsrII). Nitrates 6-13 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 9029135-7 1997 Analysis of the IL-8-alpha 2m interaction using SDS-PAGE gels indicated that the binding was mainly noncovalent. Sodium Dodecyl Sulfate 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 9033286-8 1997 NaF induced dose-dependent cytotoxicity (up to approximately 90% vital dye uptake and increased [3H]C20:4 release). Tritium 97-99 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 9081687-0 1997 Macrophages isolated from human atherosclerotic plaques produce IL-8, and oxysterols may have a regulatory function for IL-8 production. Oxysterols 74-84 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 9081687-5 1997 When monocytes and monocyte-derived macrophages, in vitro, were exposed to a series of different oxysterols, we found that all oxysterols tested had a tendency to stimulate IL-8 production but that 25-hydroxycholesterol was the most potent one. Oxysterols 127-137 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 9081687-6 1997 This stimulation of IL-8 production was time and dose dependent and could be blocked by cycloheximide. Cycloheximide 88-101 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 9343954-5 1997 EDTA and bestatin could block this downregulation of IL-8 receptor. Edetic Acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9040477-5 1997 RESULTS: Although DEX (10(-8) to 10(-6) M) inhibited IL-1 beta-stimulated MCP-1 and IL-8 production, it did not inhibit TNF-alpha-stimulated chemokine secretion. Dexamethasone 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9040477-9 1997 CONCLUSIONS: Although DEX and CSA inhibit HRPE MCP-1 and IL-8 secretion, this is dependent on whether the inducing inflammatory mediator is IL-1 beta or TNF-alpha. Dexamethasone 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 9040478-8 1997 Smaller, but significant, increases in IL-8 and MCP-1 resulted from CM phorbol myristic acid-stimulated T-lymphocytes. phorbol-12-myristate 71-92 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9040477-0 1997 Dexamethasone and cyclosporin A modulation of human retinal pigment epithelial cell monocyte chemotactic protein-1 and interleukin-8. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 119-132 9179625-7 1997 Monoclonal anti-IL-8 inhibited aurothiomalate-induced stimulation of migration. Gold Sodium Thiomalate 31-45 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 9343954-5 1997 EDTA and bestatin could block this downregulation of IL-8 receptor. ubenimex 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 9343954-7 1997 Addition of CaCl2 accelerated and depletion of Ca2+ inhibited the downregulation of the IL-8 receptor. Calcium Chloride 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 9020523-0 1997 The effects of cyclosporin A, dexamethasone and other immunomodulatory drugs on induced expression of IL-3, IL-4 and IL-8 mRNA in a human mast cell line. Cyclosporine 15-28 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 9013980-11 1997 Calcium mobilization studies using melanoma growth stimulatory activity and IL-8 suggest that a sustained loss of IL-8R B may play a part in maintaining FMLP-induced IL-8R cross-desensitization. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 9020523-0 1997 The effects of cyclosporin A, dexamethasone and other immunomodulatory drugs on induced expression of IL-3, IL-4 and IL-8 mRNA in a human mast cell line. Dexamethasone 30-43 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 9020523-2 1997 Resting cells expressed relatively low constitutive levels of mRNA for the cytokine genes IL-3, IL-4 and IL-8, and mRNA levels for each of these cytokines were significantly enhanced after 4-h stimulation with the calcium ionophore ionomycin. Calcium 214-221 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 9020523-3 1997 Treatment of the cells with the immunosuppressant CsA at 10(-5) M produced a significant inhibition of ionomycin-induced expression of IL-3, IL-4 and IL-8 mRNA, and at 10(-6) M produced a significant inhibition of induced expression of IL-3 and IL-8 but not IL-4. Cyclosporine 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 9020523-3 1997 Treatment of the cells with the immunosuppressant CsA at 10(-5) M produced a significant inhibition of ionomycin-induced expression of IL-3, IL-4 and IL-8 mRNA, and at 10(-6) M produced a significant inhibition of induced expression of IL-3 and IL-8 but not IL-4. Cyclosporine 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 9020523-3 1997 Treatment of the cells with the immunosuppressant CsA at 10(-5) M produced a significant inhibition of ionomycin-induced expression of IL-3, IL-4 and IL-8 mRNA, and at 10(-6) M produced a significant inhibition of induced expression of IL-3 and IL-8 but not IL-4. Ionomycin 103-112 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 9020523-3 1997 Treatment of the cells with the immunosuppressant CsA at 10(-5) M produced a significant inhibition of ionomycin-induced expression of IL-3, IL-4 and IL-8 mRNA, and at 10(-6) M produced a significant inhibition of induced expression of IL-3 and IL-8 but not IL-4. Ionomycin 103-112 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 9020523-5 1997 Treatment of the cells with the corticosteroid DEX at 10(-5) M but not 10(-6) M significantly reduced the ionomycin-induced expression of IL-3 but not IL-4 or IL-8 mRNA. Dextromethorphan 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 9361840-0 1997 Short chain fatty acids inhibit the expression of the neutrophil chemoattractant, interleukin 8, in the Caco-2 intestinal cell line. Fatty Acids, Volatile 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 9020026-4 1997 It was suggested that epinastine might prevent the autocrine cycle for recruitment of human eosinophils by inhibiting IL-8 release from these cells. epinastine 22-32 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 9020026-0 1997 A novel antiallergic drug epinastine inhibits IL-8 release from human eosinophils. epinastine 26-36 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 9020026-2 1997 A novel antiallergic agent epinastine showed a dose- and time-dependent suppressive effect on IL-8, one of the chemokines for eosinophils, released from eosinophils isolated from atopic diseases. epinastine 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 9020026-3 1997 The time-dependent accumulation of IL-8 inhibited by cycloheximide and the evaluation of the IL-8 mRNA levels by reverse transcriptase-polymerase chain reaction suggested that its action occurred in the posttranscriptional processes. Cycloheximide 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 11885079-6 1997 The mouthrinses containing 1% xylitol and 0.1% NaF produced the same results as 1% xylitol alone on oral glucose clearance. Xylitol 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 11885079-6 1997 The mouthrinses containing 1% xylitol and 0.1% NaF produced the same results as 1% xylitol alone on oral glucose clearance. Glucose 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 9118186-4 1997 One group brushed with a non-fluoridated toothpaste and a second with a paste containing 1,000 ppm fluoride as NaF. Fluorides 99-107 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 9025904-6 1997 Brefeldin A (BFA), colchicine, and the HMGCoA-reductase inhibitor fluvastatin disrupted the characteristic Golgi localization of IL-8, but only BFA inhibited its secretion. Brefeldin A 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 9025904-6 1997 Brefeldin A (BFA), colchicine, and the HMGCoA-reductase inhibitor fluvastatin disrupted the characteristic Golgi localization of IL-8, but only BFA inhibited its secretion. Brefeldin A 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 9025904-6 1997 Brefeldin A (BFA), colchicine, and the HMGCoA-reductase inhibitor fluvastatin disrupted the characteristic Golgi localization of IL-8, but only BFA inhibited its secretion. Colchicine 19-29 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 9025904-6 1997 Brefeldin A (BFA), colchicine, and the HMGCoA-reductase inhibitor fluvastatin disrupted the characteristic Golgi localization of IL-8, but only BFA inhibited its secretion. Fluvastatin 66-77 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 9152510-4 1997 In addition, serum selenium levels in 20 randomly selected AIDS-free individuals (CDC I: n = 10; CDC II: n = 10) were inversely correlated with serum concentrations of interleukin-8 (IL-8) and soluble tumor necrosis factor receptors (sTNFR) types I and II. Selenium 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 168-181 9152510-4 1997 In addition, serum selenium levels in 20 randomly selected AIDS-free individuals (CDC I: n = 10; CDC II: n = 10) were inversely correlated with serum concentrations of interleukin-8 (IL-8) and soluble tumor necrosis factor receptors (sTNFR) types I and II. Selenium 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 9117878-9 1997 The response to histamine was measured by PC20 (changes expressed as doubling doses: DD) IL-8 levels were obtained by ELISA, and were expressed in ng/ml. Histamine 16-25 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 9018013-6 1997 IL-8 levels in supernatants of cells stimulated with 100 U/ml of TNF-alpha for 48 h rose significantly with increasing concentrations of Et and values obtained were as follows: 4,918 +/- 244.4 pg/ml at 0 mmol/l Et, 5,335 +/- 266.2 pg/ml at 5 mmol/l Et, 8,726 +/- 873.4 pg/ml at 50 mmol/l Et and 9,134 +/- 866.0 pg/ml at 100 mmol/l Et. Ethanol 211-213 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9067093-6 1997 SCFAs and trichostatin A, structurally unrelated compounds which both induce histone hyperacetylation, both led to a dose-dependent inhibition of IL-8 gene expression. Fatty Acids, Volatile 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 9067093-6 1997 SCFAs and trichostatin A, structurally unrelated compounds which both induce histone hyperacetylation, both led to a dose-dependent inhibition of IL-8 gene expression. trichostatin A 10-24 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 9038594-0 1997 Association of antral mucosal levels of interleukin 8 and reactive oxygen radicals in patients infected with Helicobacter pylori. reactive oxygen radicals 58-82 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 9038594-6 1997 The aims of this study were to investigate if there is any association between antral mucosal levels of interleukin 8 and reactive oxygen radicals and their relationship to gastric antral inflammation. reactive oxygen radicals 122-146 C-X-C motif chemokine ligand 8 Homo sapiens 104-117 9038594-19 1997 Interleukin 8 concentration is associated with an infiltration of neutrophils and mononuclear cells and is correlated with the production of reactive oxygen radicals in antral gastric mucosa infected with Helicobacter pylori. reactive oxygen radicals 141-165 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 9038594-20 1997 These findings suggest that interleukin 8 may be important in attracting and activating phagocytes to release reactive oxygen radicals, thereby causing mucosal damage. reactive oxygen radicals 110-134 C-X-C motif chemokine ligand 8 Homo sapiens 28-41 9018013-0 1997 Enhanced interleukin-8 production by cultured Chang liver cells subjected to ethanol exposure and subsequent stimulation with tumor necrosis factor-alpha. Ethanol 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 9-22 9018013-7 1997 The chemotactic activity also increased with increasing concentrations of Et and was almost completely suppressed by anti-IL-8 antibody. Ethanol 74-76 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 9018013-6 1997 IL-8 levels in supernatants of cells stimulated with 100 U/ml of TNF-alpha for 48 h rose significantly with increasing concentrations of Et and values obtained were as follows: 4,918 +/- 244.4 pg/ml at 0 mmol/l Et, 5,335 +/- 266.2 pg/ml at 5 mmol/l Et, 8,726 +/- 873.4 pg/ml at 50 mmol/l Et and 9,134 +/- 866.0 pg/ml at 100 mmol/l Et. Ethanol 137-139 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 9238872-3 1997 2.0% Gantrez co-polymer and 0.243% NaF in a silica abrasive base. Silicon Dioxide 44-50 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 9018013-6 1997 IL-8 levels in supernatants of cells stimulated with 100 U/ml of TNF-alpha for 48 h rose significantly with increasing concentrations of Et and values obtained were as follows: 4,918 +/- 244.4 pg/ml at 0 mmol/l Et, 5,335 +/- 266.2 pg/ml at 5 mmol/l Et, 8,726 +/- 873.4 pg/ml at 50 mmol/l Et and 9,134 +/- 866.0 pg/ml at 100 mmol/l Et. Ethanol 211-213 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8989903-3 1997 Increase in O2(-)-producing capacity in MPD was also observed when other receptor-mediated agonists such as interleukin-8 and concanavalin A were used, but not when phorbol ester, a direct activator of protein kinase C, was used as the triggering agonist of O2- release. Superoxides 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 8989903-3 1997 Increase in O2(-)-producing capacity in MPD was also observed when other receptor-mediated agonists such as interleukin-8 and concanavalin A were used, but not when phorbol ester, a direct activator of protein kinase C, was used as the triggering agonist of O2- release. Superoxides 258-260 C-X-C motif chemokine ligand 8 Homo sapiens 108-121 9238873-6 1997 Results subsequent to six months of product use were as follows: At six months, the stabilized stannous fluoride dentifrice was observed to produce statistically significant 17.5% reductions in gingivitis and 27.5% reductions in gingival bleeding relative to the NaF dentifrice. Tin Fluorides 95-112 C-X-C motif chemokine ligand 8 Homo sapiens 263-266 9479645-4 1997 Notable inhibition of IL-8 secretion by human gastric cancer cells (MKN 45) was detected in the presence of sofalcone (20-100 micrograms/ml) after co-incubation with H. pylori strains. sofalcone 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 8977191-7 1997 Furthermore, inhibition of CD28 expression mediated by one representative active oligonucleotide, GR1, resulted in a concomitant dose-dependent diminution of anti-CD3/PMA-induced cytokine (IL-2, IFN-gamma, IL-8) production. Oligonucleotides 81-96 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 9479645-5 1997 In flow cytometric analysis, adherence of H. pylori strains to MKN 45 cells was significantly inhibited by treatment with sofalcone (20-60 micrograms/ml), indicating at least one reason for the inhibition of IL-8 secretion. sofalcone 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 9479645-6 1997 These results show that sofalcone is an effective mucosal protective agent that inhibits both production of VT and induction of IL-8 secretion. sofalcone 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 9055206-9 1997 The disulfide bonds have been identified by peptide mapping and sequence analysis, and are in the positions predicted by homology to interleukin-8 and platelet factor 4. Disulfides 4-13 C-X-C motif chemokine ligand 8 Homo sapiens 133-146 8985363-6 1997 Moreover, interleukin-8 (IL-8) mRNA accumulation was evident at 20 min postinfection and was induced even in the presence of cycloheximide. Cycloheximide 125-138 C-X-C motif chemokine ligand 8 Homo sapiens 10-23 8985363-6 1997 Moreover, interleukin-8 (IL-8) mRNA accumulation was evident at 20 min postinfection and was induced even in the presence of cycloheximide. Cycloheximide 125-138 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 8985363-7 1997 Both MAPK activation and IL-8 production were inhibited by forskolin, a potent inhibitor of Raf-1. Colforsin 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 9604055-1 1997 To investigate whether sodium fluoride (NaF) is able to prevent bone loss in patients treated with corticosteroids (Cs), we performed a randomized double-masked, placebo-controlled trial with 44 Cs-treated patients without established osteoporosis, defined as the absence of previous peripheral fractures and vertebral deformities on radiographs. Sodium Fluoride 23-38 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 9698935-8 1997 Furthermore, the chemotactic activity of SAL-stimulated mast cells was inhibited by antisera against IL-5 and IL-8 (interleukins). Sodium Chloride 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 9698935-9 1997 SAL-stimulated MO were only inhibited by anti-IL-8 antibodies as well SEP-stimulated mast cells. Sodium Chloride 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 9698935-10 1997 These results suggest that the EO migration induced by SAL may be dependent on resident mast cells and MO and mediated by LTB4, IL-5 and IL-8. Sodium Chloride 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 9058440-12 1997 Plasma IL-6 and IL-8 levels were marginally higher before the operation and were significantly higher on POD1 in the TPN group than in the oral group. 2',3'-dialdehyde NADP 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 9459494-4 1997 Furthermore, it is shown that NiCl2 induces mRNA expression of E-selectin, intercellular adhesion molecule-1, IL-6 and IL-8 in a 1-mM concentration. nickel chloride 30-35 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 9518388-1 1997 Using trypan blue exclusion test it has been shown that a 18 hour incubation of human erythromyeloleukosis cell line K562 together with AlF(-4) (10 mM NaF + 20 mkM AlCl3) reduced cell proliferation and survival. tetrafluoroaluminate 136-143 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 9296896-2 1997 We have examined whether the local inflammation provoked by histamine and allergen challenge of patients with atopic bronchial asthma is associated with the appearance, in vivo interleukin-B (IL-8) in bronchoalveolar lavage fluid (BAL). Histamine 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 9296896-5 1997 There was observed increased level of IL-8 (p < 0.05) after histamine and allergen challenge test. Histamine 63-72 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8989833-0 1997 Nitric oxide regulation of interleukin-8 gene expression. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 8989833-2 1997 The NO synthase inhibitor, NG-nitro-L-arginine methyl ester (L-NAME), inhibited interleukin (IL)-8 and IL-6 production in LPS-stimulated human whole blood in a dose-dependent manner. NG-Nitroarginine Methyl Ester 27-59 C-X-C motif chemokine ligand 8 Homo sapiens 80-98 8989833-2 1997 The NO synthase inhibitor, NG-nitro-L-arginine methyl ester (L-NAME), inhibited interleukin (IL)-8 and IL-6 production in LPS-stimulated human whole blood in a dose-dependent manner. NG-Nitroarginine Methyl Ester 61-67 C-X-C motif chemokine ligand 8 Homo sapiens 80-98 8989833-3 1997 In the presence of 1 microgram/mL LPS, L-NAME blocked IL-8 release (72 +/- 4% inhibition at 20 mM (mean +/- SEM, p < .05)) 24 h post-LPS without affecting cellular viability. NG-Nitroarginine Methyl Ester 39-45 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 8989833-5 1997 L-NAME inhibition of IL-8 production was also observed at the mRNA level. NG-Nitroarginine Methyl Ester 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 8989833-6 1997 Conversely, direct exposure of whole blood to NO with the spontaneous NO liberator DETA NONOate caused a dose-dependent stimulation of IL-8, but had no effect on IL-6 release. 2,2'-(hydroxynitrosohydrazono)bis-ethanamine 83-95 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 8989833-7 1997 IL-8 concentrations rose from 8.3 +/- 1.9 ng/mL at 24 h to 31.7 +/- 7.6 ng/mL at 72 h with a single stimulation of 10 mM DETA NONOate. 2,2'-(hydroxynitrosohydrazono)bis-ethanamine 121-133 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. Hydroxyl Radical 4-20 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. Hydroxyl Radical 4-20 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. Dimethyl Sulfoxide 31-49 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. Dimethyl Sulfoxide 31-49 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. Dimethyl Sulfoxide 51-55 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. Dimethyl Sulfoxide 51-55 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. 2,2'-(hydroxynitrosohydrazono)bis-ethanamine 71-83 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. 2,2'-(hydroxynitrosohydrazono)bis-ethanamine 71-83 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. Hydroxyl Radical 139-155 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 8989833-8 1997 The hydroxyl radical scavenger dimethyl sulfoxide (DMSO) prevented the DETA NONOate induction of IL-8, suggesting the participation of the hydroxyl radical in the NO-induced IL-8 production. Hydroxyl Radical 139-155 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 8978549-6 1996 We calculate the changes in the lower critical solution temperature (LCST) for the C8E5 micelle-salt-water mixture as a function of salt concentration for the salts NaF, NaCl, NaBr, NaI, and Na2SO4 and compare the trends seen with experiments. Salts 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 165-168 8978549-6 1996 We calculate the changes in the lower critical solution temperature (LCST) for the C8E5 micelle-salt-water mixture as a function of salt concentration for the salts NaF, NaCl, NaBr, NaI, and Na2SO4 and compare the trends seen with experiments. Water 101-106 C-X-C motif chemokine ligand 8 Homo sapiens 165-168 8985172-3 1996 In the first part of this study, we showed that SR 140333, an NK1 tachykinin receptor antagonist, was able to inhibit strongly the SP-induced production of interleukin (IL)-6 and IL-8 in the astrocytoma cell line. SR 140333 48-57 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 8977111-4 1996 IL-8 production in oxidized-LDL-treated cells was mediated by reactive oxygen species, as it was partially inhibited by catalase and completely inhibited by glutathione peroxidase and N-acetylcysteine (p < 0.01). Reactive Oxygen Species 62-85 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8980116-0 1996 1H NMR evidence that Glu-38 interacts with the N-terminal functional domain in interleukin-8. Hydrogen 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 8980116-0 1996 1H NMR evidence that Glu-38 interacts with the N-terminal functional domain in interleukin-8. Glutamic Acid 21-24 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 8980116-1 1996 In order to assess the importance of the buried Glu-38 observed in the structure of interleukin-8, an analog in which Glu-38 was replaced with Ala (E38A analog) was investigated by 1H NMR spectroscopy and neutrophil activation. Glutamic Acid 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 8977111-4 1996 IL-8 production in oxidized-LDL-treated cells was mediated by reactive oxygen species, as it was partially inhibited by catalase and completely inhibited by glutathione peroxidase and N-acetylcysteine (p < 0.01). Acetylcysteine 184-200 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8969274-2 1996 Recent studies in our laboratory have demonstrated that asbestos fibers stimulate lung epithelial cells to produce interleukin-8 (IL-8), the major neutrophil chemoattractant in the lung. Asbestos 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 8969274-6 1996 Asbestos fibers as well as reactive oxygen species generating systems hypoxanthine-xanthine oxidase and hydrogen peroxide stimulated DNA binding activity to the regulatory elements in the IL-8 promoter, binding sites of nuclear factor (NF)-kappaB- and NF-IL-6-like transcription factors. Reactive Oxygen Species 27-50 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 8969274-2 1996 Recent studies in our laboratory have demonstrated that asbestos fibers stimulate lung epithelial cells to produce interleukin-8 (IL-8), the major neutrophil chemoattractant in the lung. Asbestos 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 8969274-6 1996 Asbestos fibers as well as reactive oxygen species generating systems hypoxanthine-xanthine oxidase and hydrogen peroxide stimulated DNA binding activity to the regulatory elements in the IL-8 promoter, binding sites of nuclear factor (NF)-kappaB- and NF-IL-6-like transcription factors. Hydrogen Peroxide 104-121 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 8969274-8 1996 IL-8 secretion was also suppressed by staurosporine, an inhibitor of protein kinase C, and by inhibitors of tyrosine kinase such as herbimycin A and genistein. Staurosporine 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8969274-8 1996 IL-8 secretion was also suppressed by staurosporine, an inhibitor of protein kinase C, and by inhibitors of tyrosine kinase such as herbimycin A and genistein. herbimycin 132-144 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8969274-8 1996 IL-8 secretion was also suppressed by staurosporine, an inhibitor of protein kinase C, and by inhibitors of tyrosine kinase such as herbimycin A and genistein. Genistein 149-158 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8969274-9 1996 The suppression paralleled the effect of these inhibitors on asbestos-induced DNA binding to the NF-kappaB- and NF-IL-6-like binding sites of the IL-8 promoter. Asbestos 61-69 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 8969274-4 1996 Membrane permeable hydroxyl scavengers inhibited asbestos induced IL-8 expression. Hydroxyl Radical 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 8969274-10 1996 Taken together, the results suggest that asbestos-induced redox changes and phosphorylation events, mediated by staurosporine-sensitive and tyrosine kinase(s), activate nuclear proteins which recognize the NF-kappaB/NF-IL-6 binding sites of the IL-8 promoter and contribute to the regulation of IL-8 gene expression. Asbestos 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 8969274-10 1996 Taken together, the results suggest that asbestos-induced redox changes and phosphorylation events, mediated by staurosporine-sensitive and tyrosine kinase(s), activate nuclear proteins which recognize the NF-kappaB/NF-IL-6 binding sites of the IL-8 promoter and contribute to the regulation of IL-8 gene expression. Asbestos 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 295-299 8969274-5 1996 Using A549 cells transfected with the -546 IL-8 construct linked to a chloramphenicol acetyl transferase reporter gene, we have shown that these antioxidants directly inhibited asbestos-stimulated IL-8 promoter-dependent transcription. Asbestos 177-185 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 8969274-10 1996 Taken together, the results suggest that asbestos-induced redox changes and phosphorylation events, mediated by staurosporine-sensitive and tyrosine kinase(s), activate nuclear proteins which recognize the NF-kappaB/NF-IL-6 binding sites of the IL-8 promoter and contribute to the regulation of IL-8 gene expression. Staurosporine 112-125 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 8969274-5 1996 Using A549 cells transfected with the -546 IL-8 construct linked to a chloramphenicol acetyl transferase reporter gene, we have shown that these antioxidants directly inhibited asbestos-stimulated IL-8 promoter-dependent transcription. Asbestos 177-185 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 8969274-10 1996 Taken together, the results suggest that asbestos-induced redox changes and phosphorylation events, mediated by staurosporine-sensitive and tyrosine kinase(s), activate nuclear proteins which recognize the NF-kappaB/NF-IL-6 binding sites of the IL-8 promoter and contribute to the regulation of IL-8 gene expression. Staurosporine 112-125 C-X-C motif chemokine ligand 8 Homo sapiens 295-299 9010051-4 1996 SF IL-8 levels correlated strongly with CD, lactate, glucose and the lactate to glucose ratio when both disease groups were considered together (P < 0.001). Lactic Acid 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 9010051-4 1996 SF IL-8 levels correlated strongly with CD, lactate, glucose and the lactate to glucose ratio when both disease groups were considered together (P < 0.001). Glucose 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 9010051-4 1996 SF IL-8 levels correlated strongly with CD, lactate, glucose and the lactate to glucose ratio when both disease groups were considered together (P < 0.001). Lactic Acid 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 9010051-4 1996 SF IL-8 levels correlated strongly with CD, lactate, glucose and the lactate to glucose ratio when both disease groups were considered together (P < 0.001). Glucose 80-87 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 9216201-2 1996 N-acetylcysteine, an antioxidant, decreased the TNF alpha-induced expression of intercellular adhesion molecule-1 on cultured epithelial cells from human bronchi (BEAS-2A), and inhibited IL-8 production by those cells. Acetylcysteine 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 9027437-5 1996 METHOD: Interleukin-8 (1.2 x 10(-7) M) in the presence and absence of histamine was administered by intradermal injection. Histamine 70-79 C-X-C motif chemokine ligand 8 Homo sapiens 8-21 9027437-8 1996 RESULTS: In the presence of histamine, IL-8 provoked a significantly greater wheal area when compared to that produced by histamine alone (P < 0.001). Histamine 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9027437-8 1996 RESULTS: In the presence of histamine, IL-8 provoked a significantly greater wheal area when compared to that produced by histamine alone (P < 0.001). Histamine 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 9027437-9 1996 In the presence of histamine, IL-8 produced a significantly greater neutrophil infiltrate (P < 0.05), however, neither lymphocyte or eosinophil infiltration was found to be increased with IL-8 challenge. Histamine 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 9172017-0 1996 Differential regulation of TNF alpha, IL-1 beta, IL-6, IL-8, TNF beta, and IL-10 by pentoxifylline. Pentoxifylline 84-98 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 9172017-3 1996 We investigated PTX effects on production and mRNA expression of TNF alpha, IL-1 beta, IL-6, IL-8, TNF beta and IL-10. Pentoxifylline 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 9172017-8 1996 We also noted that the effects of PTX on IL-6, IL-8 and IL-10 production were different in WB and in PBMC culture. Pentoxifylline 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 9030965-5 1996 In contrast, TNF, GM-CSF and IL-8 strongly primed a subpopulation of PMN which produced large amounts of H2O2 in response to fMLP, suggesting that these cytokines may play a critical role in bactericidal killing in vivo. Hydrogen Peroxide 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 9030965-6 1996 Furthermore, we reported a decreased H2O2 production by TNF or IL-8 primed PMN in HIV-infected patients. Hydrogen Peroxide 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 8971006-3 1996 Infection with sucrose-purified RSV (pRSV) produced a time-dependent increase in the transcriptional initiation rate of the IL-8 gene. Sucrose 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8971006-3 1996 Infection with sucrose-purified RSV (pRSV) produced a time-dependent increase in the transcriptional initiation rate of the IL-8 gene. prsv 37-41 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8947075-4 1996 At concentrations of 10-100 ppb, O3 induced maximal release of interleukin-8 (IL-8), granulocyte/macrophage colony-stimulating factor (GM-CSF), tumour necrosis factor-alpha (TNF-alpha) and sICAM-1. Ozone 33-35 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 8896414-0 1996 Pyrrolidine dithiocarbamate inhibits the production of interleukin-6, interleukin-8, and granulocyte-macrophage colony-stimulating factor by human endothelial cells in response to inflammatory mediators: modulation of NF-kappa B and AP-1 transcription factors activity. pyrrolidine dithiocarbamic acid 0-27 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 8896414-4 1996 Both PDTC and NAC inhibited, in a dose-dependent manner, the synthesis of IL-6, IL-8, and GM-CSF induced by tumor necrosis factor (TNF)-alpha or bacterial lipopolysaccharides (LPS) in human umbilical vein endothelial cells (HUVEC). Acetylcysteine 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 9063511-8 1996 Comparison between the two dressings revealed significant changes in IL-8 and fibronectin mRNA levels after treatment with ClearSite, while only fibronectin changes were significant after treatment with SGS with respect to normal skin. acetylcellulose 123-132 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 8990929-3 1996 Oligonucleotide TTTTCAATTCGAAGATGATT which contain the CpG motif in hexamer palindromic sequence segments in cloned DNA augmented the expression of ICAM-1 on the endothelial cells detected by FACS analysis and also augmented the gene expression of several cytokines such as interleukin-2, interleukin-6, interleukin-8 and tumor necrosis factor alpha. Oligonucleotides 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 304-349 8909257-3 1996 Inhibition of cellular transcription with actinomycin D added at 2 hours after LPS resulted in the substantial decrease of both IL-8 and TNF-alpha mRNAs, demonstrating half-lives of 4.6 and 2.3 hours, respectively. Dactinomycin 42-55 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 8909257-6 1996 Both IL-8 and TNF-alpha protein levels decreased when actinomycin D was added 2 hours after LPS stimulation. Dactinomycin 54-67 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 8955503-5 1996 We also found that both lipoteichoic acid and sialic acid stimulated concentration-dependent increases in chorion cell IL-8 production. lipoteichoic acid 24-41 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 8955503-5 1996 We also found that both lipoteichoic acid and sialic acid stimulated concentration-dependent increases in chorion cell IL-8 production. N-Acetylneuraminic Acid 46-57 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 8955503-7 1996 Two strains of GBS tested induced concentration-dependent increases in both IL-8 and MIP-1 alpha, but both stimulated IL-8 production to a greater extent. gbs 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 8955503-7 1996 Two strains of GBS tested induced concentration-dependent increases in both IL-8 and MIP-1 alpha, but both stimulated IL-8 production to a greater extent. gbs 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 8912630-0 1996 Fas-mediated stimulation induces IL-8 secretion by rheumatoid arthritis synoviocytes independently of CPP32-mediated apoptosis. ammonium ferrous sulfate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 8947075-4 1996 At concentrations of 10-100 ppb, O3 induced maximal release of interleukin-8 (IL-8), granulocyte/macrophage colony-stimulating factor (GM-CSF), tumour necrosis factor-alpha (TNF-alpha) and sICAM-1. Ozone 33-35 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 8947075-6 1996 10(-5) M nedocromil sodium significantly attenuated the O3-induced release of both IL-8 and GM-CSF (p<0.01). Nedocromil 9-26 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 8947075-6 1996 10(-5) M nedocromil sodium significantly attenuated the O3-induced release of both IL-8 and GM-CSF (p<0.01). Ozone 56-58 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 8947075-8 1996 Similarly, the antioxidant, glutathione, at concentrations of 400-600 microM, significantly reduced the O3-induced release of IL-8 (p<0.05). Glutathione 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 8947075-8 1996 Similarly, the antioxidant, glutathione, at concentrations of 400-600 microM, significantly reduced the O3-induced release of IL-8 (p<0.05). Ozone 104-106 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 9024987-7 1996 Tepoxalin also inhibited the secretion of a NF-kappa B regulated chemokine, IL-8, a known inducer of CD11b/CD18 expression. tepoxalin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 8910351-8 1996 Modeling of the complete salt dependence of Kapp for wild-type, K3A, and R4T gp32s in NaCl and NaF with a simple ion-exchange model suggests that substitutions within the basic Lys3-Arg4-Lys5 sequence do not strongly modulate the net displacement of cations and anions upon poly(A) complex formation by gp32. Salts 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 9024987-8 1996 Thus the suppression of CD11b/CD18 expression by tepoxalin may involve IL-8. tepoxalin 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 8939177-2 1996 Nedocromil sodium produced a dose-related inhibition of ozone-induced IL-8 release from human bronchial epithelial cells and also attenuated the release of granulocyte macrophage colony-stimulating factor, tumor necrosis factor-alpha, and soluble intercellular adhesion molecule 1. Nedocromil 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 8951539-8 1996 Interleukin-8 had similar levels for CES (0.65 +/- 0.7 ng/10 cm2) and HD/HK (0.88 +/- 0.12 ng/10 cm2), whereas melanoma growth stimulatory activity was elevated in CES (2314 +/- 97 pg/10 cm2) compared with HD/HK (1071 +/- 55 pg/10 cm2). ARAMITE 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8961049-11 1996 The lower concentration of cefotaxime reduced the LPS-stimulated IL-8 levels. Cefotaxime 27-37 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 8961049-12 1996 Fleroxacin (100 mg/L) enhanced basal levels of IL-8. Fleroxacin 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 8915773-2 1996 Millimolar concentrations of NaF induced a significant accumulation of phosphatidylethanol (PEt) in Saos-2 cells but not in MG-63 and normal osteoblast-like cells. phosphatidylethanol 71-90 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 8915773-7 1996 The ability of NaF to induce both responses was largely dependent on the presence of extracellular calcium. Calcium 99-106 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 8915773-8 1996 The calcium ionophore A23187 reproduced the effect of NaF, and this effect was antagonized by EGTA, suggesting that PLD activation was, at least in part, a calcium-regulated event. Calcium 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 8915773-8 1996 The calcium ionophore A23187 reproduced the effect of NaF, and this effect was antagonized by EGTA, suggesting that PLD activation was, at least in part, a calcium-regulated event. Calcimycin 22-28 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 8915773-8 1996 The calcium ionophore A23187 reproduced the effect of NaF, and this effect was antagonized by EGTA, suggesting that PLD activation was, at least in part, a calcium-regulated event. Egtazic Acid 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 8915773-8 1996 The calcium ionophore A23187 reproduced the effect of NaF, and this effect was antagonized by EGTA, suggesting that PLD activation was, at least in part, a calcium-regulated event. Calcium 156-163 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 8915773-16 1996 Hence, mobilization of calcium by NaF cannot account for the enhanced PLD activation in response to PMA stimulation. Calcium 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 8961049-10 1996 Cefotaxime (200 mg/L) significantly (P < 0.05) increased the basal levels of IL-1 beta and reduced basal IL-8 concentration after 24 h of incubation. Cefotaxime 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 8915773-20 1996 We conclude that PLD activation by NaF in Saos-2 cells includes a fluoride-sensitive G protein, increases in the levels of intracellular calcium, and Arf/RhoA redistribution to membranes. Fluorides 66-74 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 8915773-20 1996 We conclude that PLD activation by NaF in Saos-2 cells includes a fluoride-sensitive G protein, increases in the levels of intracellular calcium, and Arf/RhoA redistribution to membranes. Calcium 137-144 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 8915775-1 1996 Sodium fluoride (NaF) is known to stimulate osteoblastic bone formation, but little attention has been given to the possibility that NaF also affects bone resorption and the differentiation of osteoclastic progenitor cells. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 8915775-3 1996 NaF increased cellular reduction of nitroblue tetrazolium (NBT), and this effect was strongly augmented by 1,25(OH)2D3. Nitroblue Tetrazolium 36-57 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8915775-3 1996 NaF increased cellular reduction of nitroblue tetrazolium (NBT), and this effect was strongly augmented by 1,25(OH)2D3. Nitroblue Tetrazolium 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8915775-3 1996 NaF increased cellular reduction of nitroblue tetrazolium (NBT), and this effect was strongly augmented by 1,25(OH)2D3. Calcitriol 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8915775-5 1996 Furthermore, NaF increased expression of CD11b and CD66b, and this stimulation was enhanced by adding 1,25(OH)2D3. Calcitriol 102-113 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 8915775-6 1996 The sum of these changes in classical promyelocytic cellular indices suggest: (1) that NaF stimulates the early stages of HL-60 differentiation toward a granulocyte-like cell and (2) that 1,25(OH)2D3 promotes these actions of NaF. (oh)2d3 192-199 C-X-C motif chemokine ligand 8 Homo sapiens 226-229 8915775-8 1996 NaF also increased cellular production of prostaglandin E2 (PGE2) and nitric oxide (NO) and induced expression of inducible nitric oxide synthase (iNOS); 1,25(OH)2D3 once again augmented these NaF-induced effects. Dinoprostone 42-58 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8915775-8 1996 NaF also increased cellular production of prostaglandin E2 (PGE2) and nitric oxide (NO) and induced expression of inducible nitric oxide synthase (iNOS); 1,25(OH)2D3 once again augmented these NaF-induced effects. Dinoprostone 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8915775-8 1996 NaF also increased cellular production of prostaglandin E2 (PGE2) and nitric oxide (NO) and induced expression of inducible nitric oxide synthase (iNOS); 1,25(OH)2D3 once again augmented these NaF-induced effects. Nitric Oxide 70-82 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8915775-9 1996 Similarly, NaF stimulated the production of interleukin 1 alpha (IL-1 alpha), IL-6, and tumor necrosis factor-alpha, and 1,25(OH)2D3 again strongly enhanced these effects. Calcitriol 121-132 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 8915775-10 1996 Indomethacin completely blocked stimulation of NBT reduction, NO production, and iNOS expression induced by NaF plus 1,25(OH)2D3; adding exogenous PGE2 (0.1-10 ng/ml) to these indomethacin-blocked cultures dose-dependently restored NO production. Indomethacin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 8915775-10 1996 Indomethacin completely blocked stimulation of NBT reduction, NO production, and iNOS expression induced by NaF plus 1,25(OH)2D3; adding exogenous PGE2 (0.1-10 ng/ml) to these indomethacin-blocked cultures dose-dependently restored NO production. Nitroblue Tetrazolium 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 8915775-10 1996 Indomethacin completely blocked stimulation of NBT reduction, NO production, and iNOS expression induced by NaF plus 1,25(OH)2D3; adding exogenous PGE2 (0.1-10 ng/ml) to these indomethacin-blocked cultures dose-dependently restored NO production. Dinoprostone 147-151 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 8915775-10 1996 Indomethacin completely blocked stimulation of NBT reduction, NO production, and iNOS expression induced by NaF plus 1,25(OH)2D3; adding exogenous PGE2 (0.1-10 ng/ml) to these indomethacin-blocked cultures dose-dependently restored NO production. Indomethacin 176-188 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 8915775-11 1996 These additional findings together with the observed slow onset (24-48 h) of NaF and 1,25(OH)2D3 interaction strongly suggest that 1,25(OH)2D3 acts as a cofactor with NaF primarily through interaction with an endogenous NaF-induced cyclo-oxygenase product(s), quite possibly PGE2 itself. Calcitriol 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 8915775-11 1996 These additional findings together with the observed slow onset (24-48 h) of NaF and 1,25(OH)2D3 interaction strongly suggest that 1,25(OH)2D3 acts as a cofactor with NaF primarily through interaction with an endogenous NaF-induced cyclo-oxygenase product(s), quite possibly PGE2 itself. Calcitriol 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 8915775-11 1996 These additional findings together with the observed slow onset (24-48 h) of NaF and 1,25(OH)2D3 interaction strongly suggest that 1,25(OH)2D3 acts as a cofactor with NaF primarily through interaction with an endogenous NaF-induced cyclo-oxygenase product(s), quite possibly PGE2 itself. Calcitriol 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 8915775-11 1996 These additional findings together with the observed slow onset (24-48 h) of NaF and 1,25(OH)2D3 interaction strongly suggest that 1,25(OH)2D3 acts as a cofactor with NaF primarily through interaction with an endogenous NaF-induced cyclo-oxygenase product(s), quite possibly PGE2 itself. Calcitriol 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 8915775-11 1996 These additional findings together with the observed slow onset (24-48 h) of NaF and 1,25(OH)2D3 interaction strongly suggest that 1,25(OH)2D3 acts as a cofactor with NaF primarily through interaction with an endogenous NaF-induced cyclo-oxygenase product(s), quite possibly PGE2 itself. Calcitriol 131-142 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 8915775-11 1996 These additional findings together with the observed slow onset (24-48 h) of NaF and 1,25(OH)2D3 interaction strongly suggest that 1,25(OH)2D3 acts as a cofactor with NaF primarily through interaction with an endogenous NaF-induced cyclo-oxygenase product(s), quite possibly PGE2 itself. Dinoprostone 275-279 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 8951539-8 1996 Interleukin-8 had similar levels for CES (0.65 +/- 0.7 ng/10 cm2) and HD/HK (0.88 +/- 0.12 ng/10 cm2), whereas melanoma growth stimulatory activity was elevated in CES (2314 +/- 97 pg/10 cm2) compared with HD/HK (1071 +/- 55 pg/10 cm2). ARAMITE 164-167 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8915775-11 1996 These additional findings together with the observed slow onset (24-48 h) of NaF and 1,25(OH)2D3 interaction strongly suggest that 1,25(OH)2D3 acts as a cofactor with NaF primarily through interaction with an endogenous NaF-induced cyclo-oxygenase product(s), quite possibly PGE2 itself. Dinoprostone 275-279 C-X-C motif chemokine ligand 8 Homo sapiens 167-170 8915775-12 1996 Such a mechanism for NaF and 1,25(OH)2D3 interaction would be strongly analogous to the interaction we have recently demonstrated between 1,25(OH)2D3 and PGE1 on the differentiation of HL-60 cells. Calcitriol 138-149 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 8951626-12 1996 The results demonstrated that a 3% KNO3/Silica/NaF mouthwash compared to a Silica/NaF control significantly reduced CDS when evaluated by tactile and thermal stimuli. potassium nitrate 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 8915775-12 1996 Such a mechanism for NaF and 1,25(OH)2D3 interaction would be strongly analogous to the interaction we have recently demonstrated between 1,25(OH)2D3 and PGE1 on the differentiation of HL-60 cells. Alprostadil 154-158 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 8951626-12 1996 The results demonstrated that a 3% KNO3/Silica/NaF mouthwash compared to a Silica/NaF control significantly reduced CDS when evaluated by tactile and thermal stimuli. potassium nitrate 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 8951626-12 1996 The results demonstrated that a 3% KNO3/Silica/NaF mouthwash compared to a Silica/NaF control significantly reduced CDS when evaluated by tactile and thermal stimuli. Silicon Dioxide 40-46 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 8951626-12 1996 The results demonstrated that a 3% KNO3/Silica/NaF mouthwash compared to a Silica/NaF control significantly reduced CDS when evaluated by tactile and thermal stimuli. Silicon Dioxide 75-81 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 8951626-12 1996 The results demonstrated that a 3% KNO3/Silica/NaF mouthwash compared to a Silica/NaF control significantly reduced CDS when evaluated by tactile and thermal stimuli. cds 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 8951626-12 1996 The results demonstrated that a 3% KNO3/Silica/NaF mouthwash compared to a Silica/NaF control significantly reduced CDS when evaluated by tactile and thermal stimuli. cds 116-119 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 8951626-13 1996 A 3% KNO3/silica/NaF mouthwash would, therefore appear to have therapeutic potential to alleviate CDS. cds 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 8810307-1 1996 The capacity of neutrophils to generate superoxide (O-2) can be enhanced by prior exposure to "priming" agents such as interleukin-8 (IL-8), melanoma growth-stimulatory activity (MGSA), and neutrophil-activating peptide (ENA-78). Superoxides 40-50 C-X-C motif chemokine ligand 8 Homo sapiens 119-132 8906207-5 1996 Among mast-cell mediators, histamine was already known to induce a rapid and transient expression of P-selectin; we demonstrated that histamine also induced an IL-6 and IL-8 secretion by HUVEC, which was concentration-dependent and inhibited by H1 or H2 receptor antagonists. Histamine 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 8906207-5 1996 Among mast-cell mediators, histamine was already known to induce a rapid and transient expression of P-selectin; we demonstrated that histamine also induced an IL-6 and IL-8 secretion by HUVEC, which was concentration-dependent and inhibited by H1 or H2 receptor antagonists. Histamine 134-143 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 8974126-7 1996 Although Il-6 and TNF production were again unchanged, there was a significant reduction in IL-8 production in the glutamine-supplemented group. Glutamine 115-124 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 8900181-7 1996 The simultaneous treatment with ATRA and TNF-alpha also resulted in changes in the composition of NF-kappaB complexes bound to the IL-8 NF-kappaB site, preventing the formation of two TNF-alpha-inducible binding activities. Tretinoin 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 8810307-1 1996 The capacity of neutrophils to generate superoxide (O-2) can be enhanced by prior exposure to "priming" agents such as interleukin-8 (IL-8), melanoma growth-stimulatory activity (MGSA), and neutrophil-activating peptide (ENA-78). Superoxides 40-50 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 8810307-1 1996 The capacity of neutrophils to generate superoxide (O-2) can be enhanced by prior exposure to "priming" agents such as interleukin-8 (IL-8), melanoma growth-stimulatory activity (MGSA), and neutrophil-activating peptide (ENA-78). Superoxides 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 119-132 8810307-1 1996 The capacity of neutrophils to generate superoxide (O-2) can be enhanced by prior exposure to "priming" agents such as interleukin-8 (IL-8), melanoma growth-stimulatory activity (MGSA), and neutrophil-activating peptide (ENA-78). Superoxides 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 8943539-8 1996 Decidua IL-8 concentrations were significantly increased (P = 0.019) 6 h after mifepristone and decidual MCP-1 concentration rose (non-significant) and fell significantly (P = 0.029) between 6 and 12 h after mifepristone. Mifepristone 79-91 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 8931876-0 1996 Arsenic induces interleukin-8 expression in cultured keratinocytes. Arsenic 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 8900430-7 1996 BH101 produced large amounts of IL-1beta, IL-6 and IL-8. bh101 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 8941999-2 1996 The concentration of IL-8 and E-alpha 1 PI in infants with CLD was low in the first 48 h of life, but dramatically increased after 48 h. The concentration of IL-8 between 48 h of life and day 5 was significantly correlated to the fraction of inspired oxygen concentration (FiO2) within 48 h of age, but not to the mean airway pressure. Oxygen 251-257 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 8941999-2 1996 The concentration of IL-8 and E-alpha 1 PI in infants with CLD was low in the first 48 h of life, but dramatically increased after 48 h. The concentration of IL-8 between 48 h of life and day 5 was significantly correlated to the fraction of inspired oxygen concentration (FiO2) within 48 h of age, but not to the mean airway pressure. Oxygen 251-257 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 8941999-2 1996 The concentration of IL-8 and E-alpha 1 PI in infants with CLD was low in the first 48 h of life, but dramatically increased after 48 h. The concentration of IL-8 between 48 h of life and day 5 was significantly correlated to the fraction of inspired oxygen concentration (FiO2) within 48 h of age, but not to the mean airway pressure. fio2 273-277 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 8941999-2 1996 The concentration of IL-8 and E-alpha 1 PI in infants with CLD was low in the first 48 h of life, but dramatically increased after 48 h. The concentration of IL-8 between 48 h of life and day 5 was significantly correlated to the fraction of inspired oxygen concentration (FiO2) within 48 h of age, but not to the mean airway pressure. fio2 273-277 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 8980877-2 1996 For most of the chemokines (IL-8, GRO-alpha, MCP-1, MIP-1 alpha) the difference in the response of leukocytes in EDTA anticoagulated blood vs those in heparinized blood was the degree of their maximal response, with a slightly higher maximal increase in CD11b expression usually seen in cells from EDTA anticoagulated blood. Edetic Acid 113-117 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 8903513-4 1996 We first systematically mutated, in groups of two to four, all the residues in the three intracellular loops of the IL-8 type A receptor to alanine and analyzed the mutant receptors transiently expressed in 293 cells. Alanine 140-147 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 8903513-5 1996 Four residues in the second intracellular loop (Y136, L137, I139, V140) and one residue in the third intracellular loop (M241) were shown to be crucial for mediating calcium signaling in response to IL-8. Calcium 166-173 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 8903513-8 1996 Mutagenesis of the residues in the first intracellular loop had only weak effects on the mobilization of calcium induced by IL-8. Calcium 105-112 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8964083-0 1996 Cocaine down-regulates IL-2-induced peripheral blood lymphocyte IL-8 and IFN-gamma production. Cocaine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 8926090-9 1996 Although heat treatment of E. chaffeensis had no effect, periodate treatment completely abolished the ability of E. chaffeensis to induce IL-1beta, IL-8, and IL-10 mRNAs. metaperiodate 57-66 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 8971982-3 1996 With membranes exposed to exogenous labeled phosphoinositides, activation of phospholipase C with calcium, with G-proteins stimulated by GTP gamma S or NaF, or with several receptor agonists, have demonstrated that all of the components of the phosphoinositide system are retained in human brain membranes and are responsive to appropriate stimuli. Phosphatidylinositols 44-61 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 8971982-3 1996 With membranes exposed to exogenous labeled phosphoinositides, activation of phospholipase C with calcium, with G-proteins stimulated by GTP gamma S or NaF, or with several receptor agonists, have demonstrated that all of the components of the phosphoinositide system are retained in human brain membranes and are responsive to appropriate stimuli. Phosphatidylinositols 44-60 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 8946235-5 1996 Our results can be summarized as follows: a) Monocytes were stimulated to release inflammatory cytokines like IL-8 and MIP-1 alpha, particularly when silicone was involved; b) Both silicone and polyurethane stimulated thrombocytes thus resulting in the release of P-Selectin and PDGF-AB, although polyurethane was a stronger stimulus; c) Moderate complement activation was triggered by contact with either of the artificial surfaces. Silicones 181-189 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 8946235-5 1996 Our results can be summarized as follows: a) Monocytes were stimulated to release inflammatory cytokines like IL-8 and MIP-1 alpha, particularly when silicone was involved; b) Both silicone and polyurethane stimulated thrombocytes thus resulting in the release of P-Selectin and PDGF-AB, although polyurethane was a stronger stimulus; c) Moderate complement activation was triggered by contact with either of the artificial surfaces. Polyurethanes 194-206 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 8841435-4 1996 Antibodies to IL-1 alpha, IL-8, and TGF beta 1 showed intense staining in silica-injured lungs as compared to saline-instilled lungs. Silicon Dioxide 74-80 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 8823366-0 1996 Low-energy helium-neon laser irradiation stimulates interleukin-1 alpha and interleukin-8 release from cultured human keratinocytes. Helium 11-17 C-X-C motif chemokine ligand 8 Homo sapiens 76-89 8964083-5 1996 Cocaine abrogated the IL-2-induced production of IFN-gamma and IL-8 in a dose-responsive manner. Cocaine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 8964083-6 1996 Cocaine also decreased PBL IFN-gamma and IL-8 mRNA expression as determined by Northern blot and slot blot analysis. Cocaine 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 8886427-4 1996 The combined beta 1- and beta 2-adrenoceptor agonist, isoprenaline, time- (100 nM, 2-18 h) and concentration- (1-30 nM) dependently increased IL-8 protein content in the cell culture supernatant as measured by an enzyme immunosorbent assay standardized for DNA by fluoro-colorimetry. Isoproterenol 54-66 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 8870686-5 1996 The degree of inhibition by sarafotoxin was dependent on the type of activator; especially IL-8 activated migration was strongly inhibited. sarafotoxin 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 8886420-14 1996 Experiments using cycloheximide demonstrated that this synergistic effect of IL-13 and IL-1 alpha on IL-8 secretion was not through de novo protein synthesis. Cycloheximide 18-31 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 8886427-11 1996 The selective beta 2-adrenoceptor agonist salbutamol (1 microM), increased IL-8 protein similarly to isoprenaline and the cyclic AMP analogue, dibutyryl cyclic AMP (1 mM) produced a corresponding effect. Albuterol 42-52 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 8886427-13 1996 Pretreatment with isoprenaline (100 nM) followed by TNF-alpha (20 ng ml-1) increased IL-8 additively. Isoproterenol 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 8886427-15 1996 In conclusion, beta-adrenoceptor stimulation increased the release of the neutrophil chemoattractant, IL-8 in 16HBE cells, via an increase in intracellular cyclic AMP. Cyclic AMP 156-166 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 8756544-11 1996 Importantly, progesterone suppressed both basal and IL-1 alpha-stimulated IL-8 expression in stromal and granulosa-lutein cell types. Progesterone 13-25 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 8756544-13 1996 The modulation of IL-8 in these cell cultures by steroid and trophic hormones suggests that IL-8 may play an important role in the physiology of ovulation, such as timely follicular rupture and neovascularization of the corpus luteum. Steroids 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 8756544-13 1996 The modulation of IL-8 in these cell cultures by steroid and trophic hormones suggests that IL-8 may play an important role in the physiology of ovulation, such as timely follicular rupture and neovascularization of the corpus luteum. Steroids 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 9064318-12 1996 Treatment of epithelial cells with IL-8 antisense oligonucleotides resulted in decreased monolayer-associated PMN but did not influence PMN transmigration, suggesting that epithelial IL-8 production may serve as a recruitment signal for PMN to the basal surface of polarized epithelia. Oligonucleotides 50-66 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 8815874-8 1996 In contrast, activation with NaF of G-proteins coupled to phospholipase C was concentration dependently inhibited by H2O2, indicating impaired G-protein function. Hydrogen Peroxide 117-121 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 9064318-12 1996 Treatment of epithelial cells with IL-8 antisense oligonucleotides resulted in decreased monolayer-associated PMN but did not influence PMN transmigration, suggesting that epithelial IL-8 production may serve as a recruitment signal for PMN to the basal surface of polarized epithelia. Oligonucleotides 50-66 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 8876732-4 1996 Specimen exposure to 1000-ppm NaF solution increased the 24-h fluoride release from all materials, with near pre-exposure levels reached after 2-3 days. Fluorides 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 30-33 8702597-5 1996 We demonstrated IL-8-dependent receptor internalization by monitoring the density of surface 125I-labeled IL-8 binding sites and by immunofluorescence microscopy. Iodine-125 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 8702597-5 1996 We demonstrated IL-8-dependent receptor internalization by monitoring the density of surface 125I-labeled IL-8 binding sites and by immunofluorescence microscopy. Iodine-125 93-97 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 8702597-10 1996 Studies with human neutrophils pretreated with 100 nM IL-8 for 5 min revealed a positive and a negative calcium response mediated by receptors A and B, respectively. Calcium 104-111 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 8756824-2 1996 We have investigated the profile of cellular recruitment into asthmatic airways after allergen and saline exposure and its relationship to interleukin-8 (IL-8) release. Sodium Chloride 99-105 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 8830798-4 1996 Enzyme-linked immunoassay GHSA (500 micrograms/mL)-treated hRPE cells secreted levels of IL-8 and MCP-1 detectable within 4 h and reached 26.0 +/- 1.3 and 42.2 0.4 ng/10(6) cells/mL after 24 h, respectively. ghsa 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 8830798-5 1996 Induction of IL-8 and MCP-1 by GHSA at concentrations ranging from 62.5 to 3,000 micrograms/mL exhibited dose-dependent kinetics. ghsa 31-35 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 8830798-6 1996 The GHSA-induced chemokine secretion by hRPE was almost completely inhibited by actinomycin D and cycloheximide, suggesting that de novo mRNA and protein synthesis are necessary for the GHSA-induced IL-8 and MCP-1 production. ghsa 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 8830798-6 1996 The GHSA-induced chemokine secretion by hRPE was almost completely inhibited by actinomycin D and cycloheximide, suggesting that de novo mRNA and protein synthesis are necessary for the GHSA-induced IL-8 and MCP-1 production. Dactinomycin 80-93 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 8830798-6 1996 The GHSA-induced chemokine secretion by hRPE was almost completely inhibited by actinomycin D and cycloheximide, suggesting that de novo mRNA and protein synthesis are necessary for the GHSA-induced IL-8 and MCP-1 production. Cycloheximide 98-111 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 8830798-6 1996 The GHSA-induced chemokine secretion by hRPE was almost completely inhibited by actinomycin D and cycloheximide, suggesting that de novo mRNA and protein synthesis are necessary for the GHSA-induced IL-8 and MCP-1 production. ghsa 186-190 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 8830798-7 1996 Northern blot analysis of GHSA-induced hRPE IL-8 and MCP-1 mRNA expression corresponded to the time- and dose-dependent increases measured by enzyme-linked immunosorbent assay. ghsa 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 8830798-8 1996 High concentrations of glucose (20 mM; 360 mg/dl) increased GHSA-induced hRPE IL-8 and MCP-1 secretion, whereas added insulin (0.5 ng/mL) inhibited IL-8 but not MCP-1 protein secretion and mRNA expression. Glucose 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 8830798-8 1996 High concentrations of glucose (20 mM; 360 mg/dl) increased GHSA-induced hRPE IL-8 and MCP-1 secretion, whereas added insulin (0.5 ng/mL) inhibited IL-8 but not MCP-1 protein secretion and mRNA expression. ghsa 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 8830798-8 1996 High concentrations of glucose (20 mM; 360 mg/dl) increased GHSA-induced hRPE IL-8 and MCP-1 secretion, whereas added insulin (0.5 ng/mL) inhibited IL-8 but not MCP-1 protein secretion and mRNA expression. ghsa 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 21594484-0 1996 Biosynthesis of IL-8 and endothelin-1,2 by immortal simian virus 40 tsA-transformed human endothelial cells. trichostatin A 68-71 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 8702797-1 1996 IL-8 and Gro-alpha differentially stimulate calcium influx through IL-8 receptors A and B. Calcium 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8702797-1 1996 IL-8 and Gro-alpha differentially stimulate calcium influx through IL-8 receptors A and B. Calcium 44-51 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 8702797-4 1996 In this study, we have evaluated the effects of IL-8 and Gro-alpha on the rate of calcium influx in human neutrophils and in 293 cells transfected with type A or type B IL-8 receptors. Calcium 82-89 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 8765098-2 1996 Inhibition of ryanodine binding was obtained by preincubation of SR membranes with ATP + NaF . Ryanodine 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 8765098-10 1996 Furthermore, a linear relationship was obtained between the degree of ryanodine binding inhibition and the level of phosphorylation of the 160/150-kDa proteins, as controlled by ATP or NaF concentrations. Ryanodine 70-79 C-X-C motif chemokine ligand 8 Homo sapiens 185-188 8756824-10 1996 There was a significant correlation between neutrophil numbers and IL-8 concentrations 4 h after saline exposure. Sodium Chloride 97-103 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 8886829-0 1996 The IL-8 production in endothelial cells is stimulated by high glucose. Glucose 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 8770057-8 1996 Both amiloride and ribavirin inhibited IL-8 mRNA induction. Amiloride 5-14 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 8770057-8 1996 Both amiloride and ribavirin inhibited IL-8 mRNA induction. Ribavirin 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 8770057-12 1996 Amiloride also inhibited IL-8 release from A549 cells stimulated with IL-1 or tumor necrosis factor. Amiloride 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 8770057-13 1996 Amiloride similarly inhibited IL-8 protein release from primary human airway epithelium infected with RSV. Amiloride 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 8894442-7 1996 IL-3 and GM-CSF were more potent in increasing the murabutide-induced response, eliciting synergistic effects on IL-8 and IL-1Ra production, at both the mRNA accumulation and the protein release. murabutide 51-61 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 8757810-6 1996 The major capsular polysaccharide, glucuronoxylomannan, stimulated release of tumor necrosis factor alpha, IL-1beta, and IL-8 in a dose-dependent fashion. Polysaccharides 19-33 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 8757810-6 1996 The major capsular polysaccharide, glucuronoxylomannan, stimulated release of tumor necrosis factor alpha, IL-1beta, and IL-8 in a dose-dependent fashion. glucuronoxylomannan 35-54 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 8877727-3 1996 This enhanced expression of IL-8 was inhibited by cycloheximide or actinomycin-D. Cycloheximide 50-63 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 8768798-6 1996 After different cellular activation either with the Ca ionophore A23187, the tripeptide formyl-methionyl-leucyl-phenylalanine (fMLP) or sodium fluoride (NaF) coincubation of PMN with APS led to a diminished generation of LTB4. Sodium Fluoride 136-151 C-X-C motif chemokine ligand 8 Homo sapiens 153-156 8768798-8 1996 However, cells which were preactivated with APS and subsequently washed showed an increase in leukotriene formation after stimulation with fMLP or NaF but not with the Ca ionophore. Leukotrienes 94-105 C-X-C motif chemokine ligand 8 Homo sapiens 147-150 8877727-3 1996 This enhanced expression of IL-8 was inhibited by cycloheximide or actinomycin-D. Dactinomycin 67-80 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 8663853-8 1996 CONCLUSIONS: Pretreatment with sheep anti-TNF-alpha Fab suppresses Jarisch-Herxheimer reactions that occur after penicillin treatment for louse-borne relapsing fever, reduces the associated increases in plasma concentrations of interleukin-6 and interleukin-8, and may be useful in other forms of sepsis. Penicillins 113-123 C-X-C motif chemokine ligand 8 Homo sapiens 246-259 8831194-9 1996 We gave some evidences of macrolides effectiveness which these drugs inhibited IL-8 production. Macrolides 26-36 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 8812652-6 1996 Mutagenesis studies of the amino-terminal region of IL-8 showed that a tripeptide, ELR, was essential for the interaction with Site 2. tripeptide K-26 71-81 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 8754823-9 1996 Cellular mRNA levels of vascular endothelial growth factor and interleukin-8 (IL-8), but not those of transforming growth factor alpha, were increased after treatment with 0.5 mM H2O2. Hydrogen Peroxide 179-183 C-X-C motif chemokine ligand 8 Homo sapiens 63-76 8754823-9 1996 Cellular mRNA levels of vascular endothelial growth factor and interleukin-8 (IL-8), but not those of transforming growth factor alpha, were increased after treatment with 0.5 mM H2O2. Hydrogen Peroxide 179-183 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 8754823-10 1996 Coadministration of anti-IL-8 antibody inhibited tubular morphogenesis enhanced by H2O2, and IL-8 itself also enhanced the formation of tube-like structures. Hydrogen Peroxide 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 8754823-11 1996 Treatment with antisense NF-kappaB oligonucleotide completely blocked H2O2-dependent IL-8 production by endothelial cells. Oligonucleotides 35-50 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 8812657-2 1996 In one study, with an ELISA of higher sensitivity, mean serum IL-8 concentration was 2 &plusmn; 0.2 pm. Adenosine Monophosphate 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 8754823-11 1996 Treatment with antisense NF-kappaB oligonucleotide completely blocked H2O2-dependent IL-8 production by endothelial cells. Hydrogen Peroxide 70-74 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 8686749-4 1996 Although retinoic-acid-treated and untreated tumor cells make the same amount of interleukin-8, the major inducer of neovascularization produced by such tumor lines, they vary in production of inhibitory activity. Tretinoin 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 8663179-5 1996 The suppressive effect of dexamethasone on IL-1beta-induced IL-8 mRNA was not observed in the presence of cycloheximide (5 microg/ml), indicating that the dexamethasone-mediated repression of IL-8 gene expression also depends on new protein synthesis. Dexamethasone 155-168 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 8663179-6 1996 Experiments with actinomycin D demonstrated that IL-8 mRNA is long-lived and that glucocorticoids down-regulate IL-8 gene expression mainly by decreasing the mRNA stability in normal HBMS cells. Dactinomycin 17-30 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 8663179-9 1996 Because curcumin (20 microM), an inhibitor of c-jun/AP-1 and protein kinases, also blocked IL-1beta-stimulated IL-8 gene expression implicating c-JUN/AP-1 and protein phosphorylation in the induction of IL-8 gene expression by IL-1beta, we conclude that the regulation of IL-8 mRNA by IL-1beta is mediated via protein kinase-dependent signal transduction pathways. Curcumin 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 8663179-9 1996 Because curcumin (20 microM), an inhibitor of c-jun/AP-1 and protein kinases, also blocked IL-1beta-stimulated IL-8 gene expression implicating c-JUN/AP-1 and protein phosphorylation in the induction of IL-8 gene expression by IL-1beta, we conclude that the regulation of IL-8 mRNA by IL-1beta is mediated via protein kinase-dependent signal transduction pathways. Curcumin 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 8663179-9 1996 Because curcumin (20 microM), an inhibitor of c-jun/AP-1 and protein kinases, also blocked IL-1beta-stimulated IL-8 gene expression implicating c-JUN/AP-1 and protein phosphorylation in the induction of IL-8 gene expression by IL-1beta, we conclude that the regulation of IL-8 mRNA by IL-1beta is mediated via protein kinase-dependent signal transduction pathways. Curcumin 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 8695787-0 1996 Presence of autoantibodies to interleukin-8 or neutrophil-activating peptide-2 in patients with heparin-associated thrombocytopenia. Heparin 96-103 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 8695787-5 1996 Five of these nine patients with anti-IL-8 or anti-NAP-2 developed thrombosis during heparin treatment, which is not statistically different from the patients with H-PF4 antibodies. Heparin 85-92 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8663179-4 1996 Both synthetic and natural glucocorticoids dexamethasone (10(-7)-10(-10) M) and hydrocortisone (10(-6)-10(-8) M) inhibited IL-1beta-stimulated IL-8 mRNA expression. Hydrocortisone 80-94 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 8663179-5 1996 The suppressive effect of dexamethasone on IL-1beta-induced IL-8 mRNA was not observed in the presence of cycloheximide (5 microg/ml), indicating that the dexamethasone-mediated repression of IL-8 gene expression also depends on new protein synthesis. Dexamethasone 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 8663179-5 1996 The suppressive effect of dexamethasone on IL-1beta-induced IL-8 mRNA was not observed in the presence of cycloheximide (5 microg/ml), indicating that the dexamethasone-mediated repression of IL-8 gene expression also depends on new protein synthesis. Dexamethasone 26-39 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 8663179-5 1996 The suppressive effect of dexamethasone on IL-1beta-induced IL-8 mRNA was not observed in the presence of cycloheximide (5 microg/ml), indicating that the dexamethasone-mediated repression of IL-8 gene expression also depends on new protein synthesis. Dexamethasone 155-168 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 8712682-5 1996 TPA per se has no effect on [Ca2+]i, but potently reverses the NaF or ionomycin induced [Ca2+]i rise. Tetradecanoylphorbol Acetate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 8712682-6 1996 Also, TPA partially counteracted the acidification induced by NaF. Tetradecanoylphorbol Acetate 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 8712682-7 1996 Both NaF and ionomycin per se had no effect on cell growth but partially counteracted TPA induced growth inhibition. Tetradecanoylphorbol Acetate 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 8920803-1 1996 Heavy metal-induced contact eczematous human skin reactions to cobalt chloride and mercuric chloride were investigated for immunoreactivity to interleukin-8 (IL-8), by using an indirect immunoperoxidase staining technique. Metals 6-11 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 8920803-1 1996 Heavy metal-induced contact eczematous human skin reactions to cobalt chloride and mercuric chloride were investigated for immunoreactivity to interleukin-8 (IL-8), by using an indirect immunoperoxidase staining technique. cobaltous chloride 63-78 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 8840238-5 1996 A significant correlation was observed between plasma IL-8 levels and serum bilirubin levels (r = 0.72; P < 0.001). Bilirubin 76-85 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 8841838-2 1996 We now report that pentamidine inhibited the human whole blood production of the chemotactic cytokines (chemokines) interleukin (IL)-8, growth related gene alpha (GRO alpha) and monocyte chemotactic protein-1 (MCP-1). Pentamidine 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 116-134 8841838-5 1996 Time course experiments indicated that pentamidine (10 microM) retained its ability to inhibit PHA-stimulated IL-8 production even when its addition was delayed for up to 24h after mitogen stimulation. Pentamidine 39-50 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 8884543-0 1996 Relationship between serum 3,5,3"-triiodothyronine and serum interleukin-8, interleukin-10 or interferon gamma in patients with nonthyroidal illness. 3,5,3"-triiodothyronine 27-50 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 8796788-1 1996 The objective of this study was to characterize interleukin-1, -6, and -8 (IL-1-, IL-6-, and IL-8)-induced prostacyclin (PGI2 as 6-keto PGF1 alpha) and prostaglandin E2 (PGE2) production in primary cultures of human myometrial cells. Epoprostenol 107-119 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 8796788-1 1996 The objective of this study was to characterize interleukin-1, -6, and -8 (IL-1-, IL-6-, and IL-8)-induced prostacyclin (PGI2 as 6-keto PGF1 alpha) and prostaglandin E2 (PGE2) production in primary cultures of human myometrial cells. Epoprostenol 121-125 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 8796788-1 1996 The objective of this study was to characterize interleukin-1, -6, and -8 (IL-1-, IL-6-, and IL-8)-induced prostacyclin (PGI2 as 6-keto PGF1 alpha) and prostaglandin E2 (PGE2) production in primary cultures of human myometrial cells. 6-keto pgf1 129-140 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 8796788-1 1996 The objective of this study was to characterize interleukin-1, -6, and -8 (IL-1-, IL-6-, and IL-8)-induced prostacyclin (PGI2 as 6-keto PGF1 alpha) and prostaglandin E2 (PGE2) production in primary cultures of human myometrial cells. Dinoprostone 152-168 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 8699129-8 1996 This unidirectional heterologous desensitization was observed with respect to both calcium mobilization and arachidonic acid production (i.e., prestimulation of the IL-8 receptor had no effect on subsequent stimulation by either fMLP or C5a). Calcium 83-90 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 8699129-8 1996 This unidirectional heterologous desensitization was observed with respect to both calcium mobilization and arachidonic acid production (i.e., prestimulation of the IL-8 receptor had no effect on subsequent stimulation by either fMLP or C5a). Arachidonic Acid 108-124 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 8639799-5 1996 By contrast, the propidium iodide (PI) staining of the DNA content showed that IL-8 could prolong the survival of resting B-CLL cells in 11 of 16 cases studied. Propidium 17-33 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 8692878-7 1996 Superoxide production, a measure of the respiratory burst, was obtained with increasing concentrations of IL-8 with maximum effects at 25 to 50 nM, but no response was observed upon challenge with GRO alpha or NAP-2 up to 1000 nM. Superoxides 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 8692878-8 1996 The superoxide production induced by IL-8 was inhibited by anti-IL8R1, but was not affected by anti-IL8R2. Superoxides 4-14 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 8648135-8 1996 Release of IL-8 protein and storage of IL-4 and IL-10 proteins were enhanced by exogenous IL-5 and inhibited by a transcription inhibitor, actinomycin D. Dactinomycin 139-152 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 8726037-0 1996 Inhibitory effect of erythromycin on interleukin 8 production by 1 alpha,25-dihydroxyvitamin D3-stimulated THP-1 cells. Erythromycin 21-33 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 8726037-0 1996 Inhibitory effect of erythromycin on interleukin 8 production by 1 alpha,25-dihydroxyvitamin D3-stimulated THP-1 cells. Calcitriol 65-95 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 8726037-1 1996 We have recently reported that long-term administration of erythromycin at a low dose reduced the number of neutrophils and concentrations of interleukin 8 (IL-8) in bronchoalveolar lavage fluid in patients with chronic lower respiratory tract disease. Erythromycin 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 142-155 8726037-1 1996 We have recently reported that long-term administration of erythromycin at a low dose reduced the number of neutrophils and concentrations of interleukin 8 (IL-8) in bronchoalveolar lavage fluid in patients with chronic lower respiratory tract disease. Erythromycin 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 157-161 8726037-2 1996 To investigate the mechanism of action of erythromycin, we evaluated its effect on IL-8 production in the 1 alpha,25-dihydroxyvitamin D3-stimulated human monocytic cell line THP-1. Erythromycin 42-54 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 8726037-3 1996 Erythromycin at a concentration of 10 micrograms/ml significantly reduced IL-8 production by THP-1 cells stimulated with lipopolysaccharide (10 ng/ml) and 1% normal human serum compared with the amount produced by untreated cells (untreated cells, 2,448 pg/ml; erythromycin-treated cells, 872 pg/ml). Erythromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 8726037-4 1996 Our results suggest that erythromycin may impair IL-8 production by alveolar macrophages, ultimately reducing neutrophil accumulation in the airspace. Erythromycin 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 11866799-4 1996 Macrolide therapy caused a significant reduction in the percentage of neutrophils, NCA and mean IL-1beta, IL-8 and LTB4 concentration in BAL fluid of the patients. Macrolides 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 11866799-6 1996 We also evaluated the in vitro inhibitory effects of macrolides on IL---8 production by vitamin D3-induced human monocytic cell line THP-1 cells when stimulated with lipopolysaccharide and serum. Macrolides 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 67-73 11866799-6 1996 We also evaluated the in vitro inhibitory effects of macrolides on IL---8 production by vitamin D3-induced human monocytic cell line THP-1 cells when stimulated with lipopolysaccharide and serum. Cholecalciferol 88-98 C-X-C motif chemokine ligand 8 Homo sapiens 67-73 8658945-0 1996 Evaluation of plasma IL-8 (CINC) concentration during ischemia and after reperfusion in the small intestine. Zinc 27-31 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 8796788-1 1996 The objective of this study was to characterize interleukin-1, -6, and -8 (IL-1-, IL-6-, and IL-8)-induced prostacyclin (PGI2 as 6-keto PGF1 alpha) and prostaglandin E2 (PGE2) production in primary cultures of human myometrial cells. Dinoprostone 170-174 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 8764366-2 1996 We demonstrate here that U-73122 caused a concentration-dependent (10-800 nM) inhibition of N-formyl-methionyl-leucyl-phenylalanine, tumor necrosis factor-alpha (TNF alpha), interleukin-8 and phorbol myristate acetate (PMA)-triggered PMN adhesion on fibronectin, fetal bovine serum or keyhole limpet hemocyanincoated microtiter plates. 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 174-187 8764366-4 1996 Further, U-73122 suppressed interleukin-8, N-formylmethionyl-leucyl-phenylalanine and PMA-stimulated up-regulation of the beta 2-integrin, Mac-1 (CD11b/CD18), on the PMN surface (IC50 < 1.3 microM). 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 9-16 C-X-C motif chemokine ligand 8 Homo sapiens 28-41 8639799-6 1996 In the remaining 5 cases, 90.6% +/- 4.39% SD of the cells after culture remained viable and IL-8 could exert a significant death protection action after pretreatment with 10(-4) mol/L hydrocortisone, which reduced the percentage of viable B-CLL cells. Hydrocortisone 184-198 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 8636420-8 1996 It was further demonstrated that AFC and farnesol inhibited KCl and NaF-induced contractions, suggesting a complex action on Ca2+ channels and G protein-dependent pathways. N-acetyl-S-farnesylcysteine 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 8787547-0 1996 Antioncogene P53 and mitogenic cytokine interleukin-8 aberrantly expressed in psoriatic skin are inversely regulated by the antipsoriatic drug tacrolimus (FK506). Tacrolimus 143-153 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 8787547-0 1996 Antioncogene P53 and mitogenic cytokine interleukin-8 aberrantly expressed in psoriatic skin are inversely regulated by the antipsoriatic drug tacrolimus (FK506). Tacrolimus 155-160 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 8787547-6 1996 After 1-3 hr, IL-8 mRNA levels were dose-dependently decreased in tacrolimus (FK506)-treated cells. Tacrolimus 66-76 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 8787547-6 1996 After 1-3 hr, IL-8 mRNA levels were dose-dependently decreased in tacrolimus (FK506)-treated cells. Tacrolimus 78-83 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 8787547-11 1996 Together with earlier results showing downmodulation for IL-8 receptor type A expression in cultured KC treated with FK506, these results suggest that both the mitogenic IL-8/IL-8R system and the cell cycle inhibitor p53 represent potential targets for the antipsoriatic action of the drug, whereas protooncogenes acting downstream in mitogenic signal transduction cascades are unaffected. Tacrolimus 117-122 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 8787547-11 1996 Together with earlier results showing downmodulation for IL-8 receptor type A expression in cultured KC treated with FK506, these results suggest that both the mitogenic IL-8/IL-8R system and the cell cycle inhibitor p53 represent potential targets for the antipsoriatic action of the drug, whereas protooncogenes acting downstream in mitogenic signal transduction cascades are unaffected. Tacrolimus 117-122 C-X-C motif chemokine ligand 8 Homo sapiens 170-174 8636420-8 1996 It was further demonstrated that AFC and farnesol inhibited KCl and NaF-induced contractions, suggesting a complex action on Ca2+ channels and G protein-dependent pathways. Farnesol 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 8738804-8 1996 Both proteinase 3-and elastase-mediated production of IL-8 was inhibited by cycloheximide, indicating de novo synthesis. Cycloheximide 76-89 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 8737641-4 1996 After an oral of NaF, all plasma fluoride is diffusible. Fluorides 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 8737641-6 1996 The area under the curve of total plasma fluoride for MFP (1540 +/- 117 mumol.min/l) doubles that of NaF (811 +/- 52 mumol.min/l p < 0.001). Fluorides 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 8737641-7 1996 On this basis, in agreement with findings previously reported for the rat, it is concluded that the bioavailability of fluoride for MFP doubles that of NaF. Fluorides 119-127 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 8724299-4 1996 While all cytokines were markedly stimulated by IL-1 alpha), co-addition of the cyclooxygenase inhibitor indomethacin enhanced IL-8 and GMCSF levels, but caused a reduction in IL-6 expression. Indomethacin 105-117 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 8724299-6 1996 PGE2 and illoprost (PGI2 analog) enhanced IL-8 production in stimulated cells. Dinoprostone 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 8724299-0 1996 Prostaglandin E2 enhances interleukin 8 (IL-8) and IL-6 but inhibits GMCSF production by IL-1 stimulated human synovial fibroblasts in vitro. Dinoprostone 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 26-39 8724299-6 1996 PGE2 and illoprost (PGI2 analog) enhanced IL-8 production in stimulated cells. illoprost 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 8724299-0 1996 Prostaglandin E2 enhances interleukin 8 (IL-8) and IL-6 but inhibits GMCSF production by IL-1 stimulated human synovial fibroblasts in vitro. Dinoprostone 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 8724299-6 1996 PGE2 and illoprost (PGI2 analog) enhanced IL-8 production in stimulated cells. Epoprostenol 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 9414445-9 1996 In contrast, the pro-inflammatory action of PGE may be involved in a synergistic action with chemokines such as IL-8 and play a role in parturition. Prostaglandins E 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 8774793-4 1996 Low oxygen levels can stimulate cellular processes, such as the production of tumor necrosis factor, interleukin (IL)-1, IL-8, and nuclear factor kappa B. Kupffer cell-mediated alterations in cocultured hepatocyte function are altered by pre-exposure to hypoxic culture conditions, whereas superoxide production, intracellular pH, and adenosine triphosphate levels are decreased by hypoxia. Oxygen 4-10 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 8645978-5 1996 After cellular preincubation with cetirizine, the amounts of LTB4 generated from neutrophil granulocytes decreased significantly when the cells were subsequently stimulated with either fMLP or NaF, in contrast to stimulations with the Ca ionophore. Cetirizine 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 193-196 8621523-0 1996 Interleukin 8 is induced by cholesterol loading of macrophages and expressed by macrophage foam cells in human atheroma. Cholesterol 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8621523-8 1996 The time course of IL-8 induction paralleled that of cholesterol loading. Cholesterol 53-64 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 8621523-12 1996 We conclude that IL-8 is induced in macrophage foam cells as a response to cholesterol loading. Cholesterol 75-86 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 8644863-4 1996 The expression of IL-8 was tested by in situ hybridization with 35S-labeled IL-8-specific RNA probes on 38 cases of HD. Sulfur-35 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 8605191-9 1996 Interestingly, the value of Gamma(salt) is independent of the salt used (NaCl, ChCl, or NaF) and is -1.5 +/- 0.1 for fibrinopeptide A and -2.5 +/- 0.1 for fibrinopeptide B. Salts 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 88-91 8613691-5 1996 Treatment with hydroxyl radical scavengers such as dimethyl sulfoxide (DMSO) will decrease the production of IL-8 in stimulated human whole blood, fibroblasts, type II epithelial cells, and hepatoma cells, but not other cytokines. Hydroxyl Radical 15-31 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 8804900-5 1996 NaOCl, NaF and APF-gel treatments caused measurable changes in intensities of the bands due to CO3(2-) and HPO4(2-); the results were found to be useful for band assignments. co3 95-98 C-X-C motif chemokine ligand 8 Homo sapiens 7-10 8804900-5 1996 NaOCl, NaF and APF-gel treatments caused measurable changes in intensities of the bands due to CO3(2-) and HPO4(2-); the results were found to be useful for band assignments. hpo4 107-111 C-X-C motif chemokine ligand 8 Homo sapiens 7-10 8804900-9 1996 This NaOCl-induced carbonate could be removed within 20 h in a 1000 ppm NaF solution. Sodium Hypochlorite 5-10 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 8804900-9 1996 This NaOCl-induced carbonate could be removed within 20 h in a 1000 ppm NaF solution. Carbonates 19-28 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 8738722-7 1996 In addition, IL-8 levels were higher in patients who died (p = 0.007), and correlated with biochemical and histological parameters, and severity of liver injury: serum aspartate aminotransferase, alanine aminotransferase, total bilirubin, prothrombin time, indocyanine green retention ratio, tumor necrosis factor-alpha and peripheral neutrophil count in patients with alcoholic hepatitis. Bilirubin 228-237 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 8738722-7 1996 In addition, IL-8 levels were higher in patients who died (p = 0.007), and correlated with biochemical and histological parameters, and severity of liver injury: serum aspartate aminotransferase, alanine aminotransferase, total bilirubin, prothrombin time, indocyanine green retention ratio, tumor necrosis factor-alpha and peripheral neutrophil count in patients with alcoholic hepatitis. Indocyanine Green 257-274 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 8812262-1 1996 Sodium fluoride (NaF; Cas No. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 8739170-2 1996 This comparative clinical 9-month study was designed to examine the efficacy of amine/stannous fluoride (AmF/SnF2) (Meridol) and sodium fluoride (NaF). Amines 58-63 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 8613691-5 1996 Treatment with hydroxyl radical scavengers such as dimethyl sulfoxide (DMSO) will decrease the production of IL-8 in stimulated human whole blood, fibroblasts, type II epithelial cells, and hepatoma cells, but not other cytokines. Dimethyl Sulfoxide 51-69 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 8613691-5 1996 Treatment with hydroxyl radical scavengers such as dimethyl sulfoxide (DMSO) will decrease the production of IL-8 in stimulated human whole blood, fibroblasts, type II epithelial cells, and hepatoma cells, but not other cytokines. Dimethyl Sulfoxide 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 8613691-7 1996 Inhibition of nitric oxide synthase will decrease production of IL-8, whereas addition of nitric oxide (NO)-generating compounds will increase production of IL-8. Nitric Oxide 14-26 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 8613691-8 1996 The hydroxyl radical appears to be the final common pathway of cell activation for IL-8 synthesis, since DMSO will inhibit the NO-driven production of IL-8. Hydroxyl Radical 4-20 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 8613691-8 1996 The hydroxyl radical appears to be the final common pathway of cell activation for IL-8 synthesis, since DMSO will inhibit the NO-driven production of IL-8. Hydroxyl Radical 4-20 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 8613691-8 1996 The hydroxyl radical appears to be the final common pathway of cell activation for IL-8 synthesis, since DMSO will inhibit the NO-driven production of IL-8. Dimethyl Sulfoxide 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 8613691-8 1996 The hydroxyl radical appears to be the final common pathway of cell activation for IL-8 synthesis, since DMSO will inhibit the NO-driven production of IL-8. Dimethyl Sulfoxide 105-109 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 8602318-2 1996 METHODS: Eighteen placentas obtained immediately after delivery were perfused with a mixture of 125I-labeled IL-8 (IL-8*) and unlabeled IL-8 in two different concentrations. Iodine-125 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 8606506-5 1996 At 1 min, DAG formation during normoxia was decreased by IL-8 plus fibronectin while hypoxia had no regulatory effect on control of DAG formation by any of the cytokines. Diglycerides 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 8606506-6 1996 In contrast to early DAG formation, hypoxia significantly downregulated late DAG formation induced by buffer without fibronectin, IL-8 plus fibronectin, and IL-1 beta with or without fibronectin. Diglycerides 77-80 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 8606506-9 1996 Thus, changes in oxygen tension can directly modulate the extent of the PMN response to stimulation by IL-8, TNF-alpha, or IL-1 beta and the G PLC-receptor pathway is particularly regulated by physiologically relevant periods of hypoxia/reoxygenation. Oxygen 17-23 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 8809187-7 1996 In this study, we found that progesterone and a synthetic progestin, medroxyprogesterone acetate (MPA) act to enhance the action of IL-1 to increase the level of IL-8 mRNA; this action of progesterone/MPA appears to be affected principally by the stabilization of IL-8 mRNA, together with a small increase in IL-8 gene transcription. Medroxyprogesterone Acetate 69-96 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 8809187-7 1996 In this study, we found that progesterone and a synthetic progestin, medroxyprogesterone acetate (MPA) act to enhance the action of IL-1 to increase the level of IL-8 mRNA; this action of progesterone/MPA appears to be affected principally by the stabilization of IL-8 mRNA, together with a small increase in IL-8 gene transcription. Medroxyprogesterone Acetate 69-96 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 8809187-7 1996 In this study, we found that progesterone and a synthetic progestin, medroxyprogesterone acetate (MPA) act to enhance the action of IL-1 to increase the level of IL-8 mRNA; this action of progesterone/MPA appears to be affected principally by the stabilization of IL-8 mRNA, together with a small increase in IL-8 gene transcription. Medroxyprogesterone Acetate 69-96 C-X-C motif chemokine ligand 8 Homo sapiens 264-268 8602318-2 1996 METHODS: Eighteen placentas obtained immediately after delivery were perfused with a mixture of 125I-labeled IL-8 (IL-8*) and unlabeled IL-8 in two different concentrations. Iodine-125 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 115-120 8602318-2 1996 METHODS: Eighteen placentas obtained immediately after delivery were perfused with a mixture of 125I-labeled IL-8 (IL-8*) and unlabeled IL-8 in two different concentrations. Iodine-125 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 8602318-9 1996 Because measurement of unlabeled IL-8 yielded negative results, the radioactivity is clearly attributable to free iodine 125, which is generated during IL radiolabeling or which disassociates from IL-8 in small amounts after radiolabeling. Iodine 114-120 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 8602318-9 1996 Because measurement of unlabeled IL-8 yielded negative results, the radioactivity is clearly attributable to free iodine 125, which is generated during IL radiolabeling or which disassociates from IL-8 in small amounts after radiolabeling. Iodine 114-120 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 8935186-7 1996 As 12-HETE has been shown to modulate the expression and production of various proteins, the consequence of the 12-HETE uptake on the release of GM-CSF and IL8 by HBEC was assessed. 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 156-159 8608955-6 1996 Induction of tax in JPX-9 with Cd2+ was accompanied by rapid induction of IL-8, IP-10, MIP-1alpha, MIP-1beta, 1309 and SCM-1 as determined by reverse transcription PCR. jpx-9 20-25 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 8707887-0 1996 Proinflammatory agents, IL-8 and IL-10, upregulate inducible nitric oxide synthase expression and nitric oxide production in avian osteoclast-like cells. Nitric Oxide 61-73 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 8640818-0 1996 Taxol-dependent transcriptional activation of IL-8 expression in a subset of human ovarian cancer. Paclitaxel 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 8640818-4 1996 Taxol induced secretion of interleukin (IL) 8 but not IL-6, IL-1alpha, or IL-1beta in 4 of 10 samples. Paclitaxel 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 27-45 8934801-7 1996 Symptom scores for nasal sneezing, pruritus, rhinorrhea, and nasal LTB4 levels at 6 and 8 hours and IL-8 at 3, 6, and 8 hours were generally lower in astemizole-treated patients compared to those on placebo. Astemizole 150-160 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 8934801-10 1996 This study is the first to demonstrate an effect of astemizole during NP on IL-8 and LTB4 levels with a significant correlation of neutrophil numbers in untreated patients during the nasal late phase response. Astemizole 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 8882622-9 1996 The non-selective PKC inhibitor, staurosporine (1-300 nM) significantly increased the production of IL-1 alpha-induced IL-8 mRNA and protein. Staurosporine 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 8882622-10 1996 A specific PKC inhibitor, chelerythrine chloride (0.1-3 microM), also caused a small concentration-dependent increase in IL-8 mRNA and protein production. chelerythrine 26-48 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 8608647-12 1996 Our results suggest that the relative amounts of IL-1beta and IL-1Ra or IL-8 may contribute, at least in part, to the neutrophil-mediated chronic airway inflammation in patients with chronic airway disease, and long-term erythromycin therapy may down-regulate the vigorous cycle between the cytokine network and neutrophil accumulation, with resultant reduction of neutrophil-mediated inflammatory response. Erythromycin 221-233 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 8604023-0 1996 IL-1 beta primes IL-8-activated human neutrophils for elastase release, phospholipase D activity, and calcium flux. Calcium 102-109 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 8675084-8 1996 Exposure to toxin A for 24 hours induced interleukin 8 production in T84 and HT29 cells. toxin a 12-19 C-X-C motif chemokine ligand 8 Homo sapiens 41-54 8675084-10 1996 During culture (in medium only), EDTA detached colonic epithelial cells produced interleukin 8 and cell death occurred by apoptosis. Edetic Acid 33-37 C-X-C motif chemokine ligand 8 Homo sapiens 81-94 8675084-11 1996 Colonic disease by C difficile may be initiated by toxin A mediated induction of epithelial cell interleukin 8 production and apoptosis after cell detachment from the basement membrane. c difficile 19-30 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 8641762-5 1996 Human peripheral blood monocytes and polymorphonuclear leukocytes secreted IL-8 when cultured in the presence of CPC. cpc 113-116 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 8617783-7 1996 The metal chelating abilities of these histidine mutants of thioredoxin were successfully utilized for convenient purifications of human interleukin-8 and -11 expressed in E. coli as soluble thioredoxin fusion proteins. Metals 4-9 C-X-C motif chemokine ligand 8 Homo sapiens 137-158 8617783-7 1996 The metal chelating abilities of these histidine mutants of thioredoxin were successfully utilized for convenient purifications of human interleukin-8 and -11 expressed in E. coli as soluble thioredoxin fusion proteins. Histidine 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 137-158 8604023-6 1996 On the contrary, it was correlated with priming of phospholipase D activity and calcium flux activated by IL-8. Calcium 80-87 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 8604023-1 1996 Interleukin-8 (IL-8), the prototype of the alpha (e.i., C-X-C branch) chemokine family, induced elastase release in a concentration-dependent manner (50-1000 ng/mL) in cytochalasin B-treated human polymorphonuclear leukocytes (PMNs). Cytochalasin B 168-182 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8604023-1 1996 Interleukin-8 (IL-8), the prototype of the alpha (e.i., C-X-C branch) chemokine family, induced elastase release in a concentration-dependent manner (50-1000 ng/mL) in cytochalasin B-treated human polymorphonuclear leukocytes (PMNs). Cytochalasin B 168-182 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 8604023-7 1996 Preincubation of the cells with ethanol and/or La3+ inhibited IL-8-induced degranulations, suggesting that activation of phospholipase D and increase of [Ca2+]i were important for this response. Ethanol 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 8604023-7 1996 Preincubation of the cells with ethanol and/or La3+ inhibited IL-8-induced degranulations, suggesting that activation of phospholipase D and increase of [Ca2+]i were important for this response. lanthanum(3+) 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 8721128-8 1996 The IL-8 increased during surgery in both groups but the increase was significantly less in the PGE1 group (P < 0.05). Alprostadil 96-100 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 8832978-12 1996 CONCLUSION: Our data suggest that TNF-alpha induces expression of proinflammatory cytokines such as IL-8 and MCP-1 through generation of reactive oxygen intermediates and subsequent activation of NF-kappa B in human synovial cells, and the antioxidants may inhibit, at least in part, the activation of NF-kappa B by TNF-alpha. reactive oxygen intermediates 137-166 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 8832978-8 1996 Prior addition of antioxidant, N-acetyl-L-cysteine (NAC) or 2-oxothiazolidine-4-carboxylate (OTC), suppressed TNF-alpha stimulated expressions of IL-8, MCP-1, and collagenase mRNA in a dose dependent manner. 2-oxothiazolidine-4-carboxylic acid 60-91 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 8721128-10 1996 We conclude that PGE1 administration suppresses TNF-alpha and IL-8 responses during pneumonectomy, but its effects on IL-6 and the postoperative status were not significant. Alprostadil 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 8779915-3 1996 Adenosine dose dependently inhibited the release of interleukin (IL)-6 and IL-8 by stimulated human umbilical vein endothelial cells (HUVEC). Adenosine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 8729095-8 1996 In further studies, DHA dose- and time-dependently reduced also the expression of E-selectin, Intercellular Adhesion Molecule-1, interleukin (IL)-6 and IL-8, in response to IL-1, IL-4, tumor-necrosis factor, or bacterial endotoxin. Docosahexaenoic Acids 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 8605000-2 1996 Interleukin-8 triggers several functions of neutrophils in host defense: chemotaxis, degranulation and enzyme release, and superoxide production. Superoxides 123-133 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8621714-1 1996 Chemical modification of the interleukin-8 Leu25 --> Cys mutant. Cysteine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 29-42 8621714-3 1996 We have previously shown that two novel CC chemokine-like properties, namely monocyte chemoattraction and binding to CC CKR-1, are introduced into IL-8 by mutating Leu25 to the conserved tyrosine present in CC chemokines. Tyrosine 187-195 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 8621714-8 1996 However, modification of the cysteine by addition of a fluorescent N-methyl-N-(2-N-methyl, N-(7-nitrobenz-2-oxa-1, 3-diazol-4-yl)aminoethyl)acetamido (NBD) group lowers potency in neutrophil chemotaxis and affinity in IL-8 receptor binding assays by 2 orders of magnitude. Cysteine 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 8621714-8 1996 However, modification of the cysteine by addition of a fluorescent N-methyl-N-(2-N-methyl, N-(7-nitrobenz-2-oxa-1, 3-diazol-4-yl)aminoethyl)acetamido (NBD) group lowers potency in neutrophil chemotaxis and affinity in IL-8 receptor binding assays by 2 orders of magnitude. n-methyl-n-(2-n-methyl, n-(7-nitrobenz-2-oxa-1, 3-diazol-4-yl)aminoethyl)acetamido (nbd 67-154 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 8576262-3 1996 IL-8 stimulation of its receptor on neutrophils activates Ras GTP loading and the mitogen-activated protein kinase (MAPK) pathway including Raf-1 and B-Raf. ras gtp 58-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8576262-9 1996 Surprisingly, wortmannin, at low concentrations, inhibits Raf-1, B-Raf, and MAPK activation in response to IL-8 and C5a demonstrating a role for phosphatidylinositol 3-kinase in the activation of Raf kinases in G protein-coupled receptor systems in human neutrophils. Wortmannin 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 8576262-10 1996 Furthermore, wortmannin inhibits IL-8 stimulated granule release and neutrophil adherence. Wortmannin 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 8777274-2 1996 The release of IL-8 was significantly higher in persons with high HDL, and was correlated with HDL, and inversely correlated with triglycerides and sCD14. Triglycerides 130-143 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 8801091-3 1996 The CSF levels of IL-8 correlated with the levels of tumor necrosis factor-alpha, leukocyte count, neutrophil count, protein level, CSF/blood glucose ratio, and the number of days patients were hospitalized. Glucose 142-149 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 8926049-0 1996 Inhibition of leukotriene formation and IL-8 release by the paf-receptor antagonist SM-12502. 3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 8926049-1 1996 We analyzed the effect of the PAF receptor antagonist (+)-cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride (SM-12502) on the release of leukotriene B4 and IL-8 from human leukocytes. (+)-cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride 54-119 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 8926049-1 1996 We analyzed the effect of the PAF receptor antagonist (+)-cis-3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one hydrochloride (SM-12502) on the release of leukotriene B4 and IL-8 from human leukocytes. 3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one 121-129 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 8926049-4 1996 The PAF receptor antagonist led to a concentration and time dependent inhibition of LTB4 formation and IL-8 release from PMN and LMB. leptomycin B 129-132 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 8926049-5 1996 Our data clearly indicate an inhibitory effect of the PAF receptor antagonist SM-12502 on the formation of mediators of the lipoxygenase pathway and on the release of IL-8. 3,5-dimethyl-2-(3-pyridyl)thiazolidin-4-one 78-86 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 8919301-1 1996 Chronic exposure of all-trans-retinoic acid-differentiated SH-SY5Y cells to morphine (10 mu M; 2 days) results in sensitization of adenylate cyclase as characterized by a significant increase in both PGE1 receptor-mediated as well as receptor-independent (NaF, 10 mM; forskolin, 100 mu M) stimulation of effector activity. Tretinoin 24-43 C-X-C motif chemokine ligand 8 Homo sapiens 256-259 8822349-1 1996 Sodium fluoride (NaF), which stimulates bone formation, and bisphosphonates, which reduce bone resorption, are both used in the treatment of osteoporosis, and are binding to bone mineral. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 8822349-6 1996 The changes produced by fluoride are in the same direction as seen in bones from patients treated with NaF, albeit much smaller. Fluorides 24-32 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 8705396-5 1996 Thus, changes in oxygen tension can directly modulate the extent of the PMN response to stimulation by IL-8, TNF-alpha, or IL-1 beta, and activation of the GPLD-pathway appears to be highly sensitive to hypoxia and hypoxia/reoxygenation. Oxygen 17-23 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 8572786-13 1996 CONCLUSIONS: Earlier steroid administration in the immunosuppressive protocol for HTx or HLTx may be preferable to reduce the inflammatory response to cardiopulmonary bypass, as reflected by a lower production of tumor necrosis factor alpha and IL-8, and a greater release of IL-10. Steroids 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 245-249 8919301-1 1996 Chronic exposure of all-trans-retinoic acid-differentiated SH-SY5Y cells to morphine (10 mu M; 2 days) results in sensitization of adenylate cyclase as characterized by a significant increase in both PGE1 receptor-mediated as well as receptor-independent (NaF, 10 mM; forskolin, 100 mu M) stimulation of effector activity. Morphine 76-84 C-X-C motif chemokine ligand 8 Homo sapiens 256-259 8557108-0 1996 Dansyl cadaverine regulates ligand induced endocytosis of interleukin-8 receptor in human polymorphonuclear neutrophils. monodansylcadaverine 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 8576166-1 1996 The glucocorticoid dexamethasone inhibited the production of the rat cytokine-induced neutrophil chemoattractant CINC/gro, a counterpart of human melanoma growth-stimulating activity that belongs to the interleukin-8 (IL-8) family, in the normal rat kidney epithelial cell line NRK-52E stimulated with interleukin-1 beta (IL-1 beta), lipopolysaccharide, or tumor necrosis factor alpha. Dexamethasone 19-32 C-X-C motif chemokine ligand 8 Homo sapiens 203-216 8576166-1 1996 The glucocorticoid dexamethasone inhibited the production of the rat cytokine-induced neutrophil chemoattractant CINC/gro, a counterpart of human melanoma growth-stimulating activity that belongs to the interleukin-8 (IL-8) family, in the normal rat kidney epithelial cell line NRK-52E stimulated with interleukin-1 beta (IL-1 beta), lipopolysaccharide, or tumor necrosis factor alpha. Dexamethasone 19-32 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 8543832-5 1996 This IL-8 gene expression was inhibited by pretreatment with 5 microM taxol, a microtubule-stabilizing agent. Paclitaxel 70-75 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 8543831-6 1996 Treatment of TPA-stimulated Mono Mac6 cells resulted in a strong potentiation of secreted IL-1 bioactivity and expression of IL-1 alpha and IL-8 mRNA. Tetradecanoylphorbol Acetate 13-16 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 8557108-4 1996 We have found that monodansyl cadaverine (MDC) inhibited about 70% of IL-8 induced endocytosis and caused 70% and 66% inhibition of IL-8 mediated chemotaxis and respiratory burst response, respectively, in neutrophils. monodansylcadaverine 19-40 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 8543832-6 1996 Colchicine or vinblastine, microtubule-disrupting agents, induced IL-8 gene expression, which was also inhibited by taxol treatment. Colchicine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 8543832-6 1996 Colchicine or vinblastine, microtubule-disrupting agents, induced IL-8 gene expression, which was also inhibited by taxol treatment. Vinblastine 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 8557108-4 1996 We have found that monodansyl cadaverine (MDC) inhibited about 70% of IL-8 induced endocytosis and caused 70% and 66% inhibition of IL-8 mediated chemotaxis and respiratory burst response, respectively, in neutrophils. monodansylcadaverine 19-40 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 8543832-6 1996 Colchicine or vinblastine, microtubule-disrupting agents, induced IL-8 gene expression, which was also inhibited by taxol treatment. Paclitaxel 116-121 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 8557108-4 1996 We have found that monodansyl cadaverine (MDC) inhibited about 70% of IL-8 induced endocytosis and caused 70% and 66% inhibition of IL-8 mediated chemotaxis and respiratory burst response, respectively, in neutrophils. monodansylcadaverine 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 8557108-4 1996 We have found that monodansyl cadaverine (MDC) inhibited about 70% of IL-8 induced endocytosis and caused 70% and 66% inhibition of IL-8 mediated chemotaxis and respiratory burst response, respectively, in neutrophils. monodansylcadaverine 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 8865864-3 1996 The aim of the present study was to examine differences in interleukin (IL)-8 expression by MC from patients with NRF and from patients with end-stage renal disease (ESRD). Methylcholanthrene 92-94 C-X-C motif chemokine ligand 8 Homo sapiens 59-77 8567958-9 1996 149: 1153-1159), we observed that treatment with CP-105,696 inhibited the acute increase in bronchoalveolar lavage (BAL) levels of IL-6 and IL-8 by 56.9 +/- 13.2% and 46.9 +/- 14.5%, respectively, 4 h after challenge with Ascaris suum antigen (Ag). cp-105 49-55 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 8865864-6 1996 The IL-8 background level of MC isolated from patients with NRF was significantly lower than the IL-8 background level of MC derived from patients with ESRD. Methylcholanthrene 29-31 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 8865864-6 1996 The IL-8 background level of MC isolated from patients with NRF was significantly lower than the IL-8 background level of MC derived from patients with ESRD. Methylcholanthrene 122-124 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 9238884-11 1996 The confidence interval calculations for both incremental DFS and DFT support the conclusion that a dentifrice containing 0.3% triclosan and 2.0% PVM/MA copolymer in a 0.331% NaF/silica (1500 ppm F) base provides a level of anticaries efficacy which is "at least as good as" that provided by a dentifrice containing 1500 NaF/silica, without those additive agents. Triclosan 127-136 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 8838968-5 1996 The effect of urinary trypsin inhibitor on the production of prostaglandin E2 (PGE2) from myometrial cultures stimulated by IL-8, IL-1 and LPS was verified. Dinoprostone 61-77 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8838968-5 1996 The effect of urinary trypsin inhibitor on the production of prostaglandin E2 (PGE2) from myometrial cultures stimulated by IL-8, IL-1 and LPS was verified. Dinoprostone 79-83 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8568122-2 1996 IL-8 inhibits MCAF-induced histamine release from basophils. Histamine 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8931954-7 1996 Following 4 days of maturation with ATRA, the cells would increase F-actin content in response to interleukin-8, ingest latex beads, migrate in a chemotaxis chamber, reduce NBT, and express CD11b. Tretinoin 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 98-111 8720280-5 1996 Alveolar macrophages cultured in vitro from the asbestos-exposed individuals spontaneously released significant amounts of the neutrophil chemotaxin, interleukin-8 (IL-8). Asbestos 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 8720280-5 1996 Alveolar macrophages cultured in vitro from the asbestos-exposed individuals spontaneously released significant amounts of the neutrophil chemotaxin, interleukin-8 (IL-8). Asbestos 48-56 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 8720280-7 1996 In vitro experiments confirmed that crocidolite or chrysotile asbestos could stimulate the release of IL-8 from mononuclear phagocytes in a dose-dependent fashion. Asbestos, Crocidolite 36-47 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 9238883-11 1996 The confidence interval calculations for both incremental DFS and DFT support the conclusion that a dentifrice containing 0.3% triclosan and 2.0% PVM/MA copolymer in a 0.243% NaF/silica (1100 ppm F) base provides a level of anticaries efficacy which is "at least as good as" that provided by a dentifrice containing 1100 NaF/silica without those additive agents. Triclosan 127-136 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 9238883-11 1996 The confidence interval calculations for both incremental DFS and DFT support the conclusion that a dentifrice containing 0.3% triclosan and 2.0% PVM/MA copolymer in a 0.243% NaF/silica (1100 ppm F) base provides a level of anticaries efficacy which is "at least as good as" that provided by a dentifrice containing 1100 NaF/silica without those additive agents. copolymer 153-162 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 9238884-11 1996 The confidence interval calculations for both incremental DFS and DFT support the conclusion that a dentifrice containing 0.3% triclosan and 2.0% PVM/MA copolymer in a 0.331% NaF/silica (1500 ppm F) base provides a level of anticaries efficacy which is "at least as good as" that provided by a dentifrice containing 1500 NaF/silica, without those additive agents. copolymer 153-162 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 8558067-10 1996 Mutations of one of the residues in this region, Leu-25 in IL-8, to tyrosine (which is conserved at this position in CC chemokines) enables the mutant IL-8 to bind CC chemokine receptor-1 (CC-CKR-1) and introduces monocyte chemoattractant activity. Leucine 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 8942140-8 1996 Furthermore, the levels of interleukin-8 and neutrophil chemotactic activity in the bronchoalveolar lavage fluid of cryptogenic organizing pneumonia patients with bronchoalveolar lavage fluid neutrophilia were significantly decreased following treatment with erythromycin. Erythromycin 259-271 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 8558067-10 1996 Mutations of one of the residues in this region, Leu-25 in IL-8, to tyrosine (which is conserved at this position in CC chemokines) enables the mutant IL-8 to bind CC chemokine receptor-1 (CC-CKR-1) and introduces monocyte chemoattractant activity. Leucine 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 8558067-10 1996 Mutations of one of the residues in this region, Leu-25 in IL-8, to tyrosine (which is conserved at this position in CC chemokines) enables the mutant IL-8 to bind CC chemokine receptor-1 (CC-CKR-1) and introduces monocyte chemoattractant activity. Tyrosine 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 8558067-10 1996 Mutations of one of the residues in this region, Leu-25 in IL-8, to tyrosine (which is conserved at this position in CC chemokines) enables the mutant IL-8 to bind CC chemokine receptor-1 (CC-CKR-1) and introduces monocyte chemoattractant activity. Tyrosine 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 8722494-11 1996 MK-886 also inhibited synovial production of two other pleiotrophic cytokines which it regulates, IL-6 and IL-8. MK-886 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 8942140-10 1996 It is possible that cryptogenic organizing pneumonia is caused by neutrophil-mediated inflammation, and that the favorable clinical effect of erythromycin is due to inhibition of neutrophil accumulation in the peripheral airways through a biological activity other than bacteriostasis, e.g., local suppression of interleukin-8 production. Erythromycin 142-154 C-X-C motif chemokine ligand 8 Homo sapiens 313-326 8734298-11 1996 In particular, TNF and IL-8 plasma levels as well as LPS-induced monocytic production of these cytokines ex vivo have been correlated with the production of ROS by stimulated PMN and with the lung injury score in patients with Adult Respiratory Distress Syndrom (ARDS). Reactive Oxygen Species 157-160 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 8747002-0 1996 Modulation of IL-1 beta, IL-6, IL-8, TNF-alpha, and TGF-beta secretions by alveolar macrophages under NO2 exposure. Nitrogen Dioxide 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 8747002-7 1996 Exposure for 30 min to NO2 induced a significant decrease of LPS-stimulated IL-1 Beta, IL-6, IL-8, and TNF-alpha (p < .05). Nitrogen Dioxide 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 8747002-10 1996 NO2 exposure of LPS-stimulated AM resulted in a functional impairment of AM after NO2 exposure regarding IL-1 beta, IL-6, IL-8, and TNF-alpha. Nitrogen Dioxide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 8883016-14 1996 In addition, the higher release of IL-1 beta and IL-8 by PMO isolated from G-PDF suggests a stronger intra-abdominal activation of PMO, with G-PDF acting as a chemical inflammatory agent. g-pdf 75-80 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 8734298-8 1996 TNF, GM-CSF and IL-8 strongly primed a subpopulation of PMN to produce H2O2 in response to fMLP, while IL-1 alpha, IL-1 beta and IL-6 failed to do so. Hydrogen Peroxide 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 8734298-9 1996 Furthermore, the addition of TNF, GM-CSF or IL-8 to whole blood increased the capacity of a subpopulation of PMN to bind N-formyl peptides, a phenomenon that could account for the strong H2O2 production in response to fMLP following priming by the cytokines. n-formyl peptides 121-138 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 8734298-9 1996 Furthermore, the addition of TNF, GM-CSF or IL-8 to whole blood increased the capacity of a subpopulation of PMN to bind N-formyl peptides, a phenomenon that could account for the strong H2O2 production in response to fMLP following priming by the cytokines. Hydrogen Peroxide 187-191 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 8734298-13 1996 In particular, in HIV infected patients we demonstrated a decrease of H2O2 production by PMN in whole blood after ex vivo priming by IL-8 and TNF followed by fMLP stimulation. Hydrogen Peroxide 70-74 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 8833992-0 1996 Interleukin 1 beta, tumor necrosis factor alpha, and interleukin 8 in bronchoalveolar lavage fluid of patients with diffuse panbronchiolitis: a potential mechanism of macrolide therapy. Macrolides 167-176 C-X-C motif chemokine ligand 8 Homo sapiens 53-66 8833992-8 1996 In addition, the concentration of IL-8 in alveolar macrophages obtained from 2 volunteers before and after oral erythromycin administration also decreased ex vivo. Erythromycin 112-124 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 8618875-3 1995 Maximal IL-8 production was seen when 40 mM salt was added (375 mosM) and was equal to IL-8 induced by endotoxin or IL-1 alpha. Salts 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 8618875-5 1995 Hyperosmolar NaCl also induced IL-8 and increased steady-state levels of IL-8 mRNA similar to those induced by IL-1 alpha. Sodium Chloride 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 8618875-5 1995 Hyperosmolar NaCl also induced IL-8 and increased steady-state levels of IL-8 mRNA similar to those induced by IL-1 alpha. Sodium Chloride 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 8618875-6 1995 IL-8 gene expression was elevated for 96 hr in peripheral blood mononuclear cells incubated with hyperosmolar NaCl. Sodium Chloride 110-114 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8618875-7 1995 In human THP-1 macrophagic cells, osmotic stimulation with KI, NaI, or NaCl also induced IL-8 production. KS I 59-61 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 8618875-7 1995 In human THP-1 macrophagic cells, osmotic stimulation with KI, NaI, or NaCl also induced IL-8 production. Sodium Iodide 63-66 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 8618875-7 1995 In human THP-1 macrophagic cells, osmotic stimulation with KI, NaI, or NaCl also induced IL-8 production. Sodium Chloride 71-75 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 8618875-9 1995 Using specific blockade of this kinase, a dose-response inhibition of hyperosmolar NaCl-induced IL-8 synthesis was observed, similar to that in cells stimulated with IL-1. Sodium Chloride 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 8647994-4 1995 NHKs secreted detectable levels of IL-8, but not of IL-6, and IL-8 secretion increased over 20 fold by stimulation with 10 nM of phorbol 12-myristate 13-acetate (PMA). Tetradecanoylphorbol Acetate 129-160 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 8526925-1 1995 Fluoride (NaF) (5-15 mM) activated the 22Na+ uptake by human red blood cells (RBC). Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 10-13 8526925-4 1995 The NaF-induced 22Na+ uptake was sensitive to tetrodotoxin (TTX), pertussis toxin but not to amiloride nor valinomycin. Tetrodotoxin 46-58 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 8526925-4 1995 The NaF-induced 22Na+ uptake was sensitive to tetrodotoxin (TTX), pertussis toxin but not to amiloride nor valinomycin. Tetrodotoxin 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 8526925-4 1995 The NaF-induced 22Na+ uptake was sensitive to tetrodotoxin (TTX), pertussis toxin but not to amiloride nor valinomycin. Amiloride 93-102 C-X-C motif chemokine ligand 8 Homo sapiens 4-7 8526925-6 1995 Thus, the TTX-sensitive Na(+)-transport system is present in the RBC membrane in an inactive form which could be activated with NaF by a mechanism involving G-protein(s) but not the depolarization. Tetrodotoxin 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 8723018-10 1995 Basal adenylyl cyclase activity increased from 33.1 +/- 2.6 40 +/- 2.4 pmol/mg protein per min; a significant increase in activity stimulated by isoproterenol (from 41.5 +/- 3.1 to 61 +/- 3.8 pmol/mg protein per min) and by NaF (from 71.8 +/- 2.7 to 85.3 +/- 3.5 pmol/mg protein per min) was also observed. Isoproterenol 145-158 C-X-C motif chemokine ligand 8 Homo sapiens 224-227 8647994-4 1995 NHKs secreted detectable levels of IL-8, but not of IL-6, and IL-8 secretion increased over 20 fold by stimulation with 10 nM of phorbol 12-myristate 13-acetate (PMA). Tetradecanoylphorbol Acetate 129-160 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 8647994-4 1995 NHKs secreted detectable levels of IL-8, but not of IL-6, and IL-8 secretion increased over 20 fold by stimulation with 10 nM of phorbol 12-myristate 13-acetate (PMA). Tetradecanoylphorbol Acetate 162-165 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 8647994-4 1995 NHKs secreted detectable levels of IL-8, but not of IL-6, and IL-8 secretion increased over 20 fold by stimulation with 10 nM of phorbol 12-myristate 13-acetate (PMA). Tetradecanoylphorbol Acetate 162-165 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 8595612-10 1995 Up-regulation of CD11b, down-regulation of L-s and release of IL8 were inversely related to heparin concentration (r = 0.87, P < 0.05). Heparin 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 8587236-0 1995 Interleukin-1-induced IL-8 and IL-6 gene expression and production in human mesangial cells is differentially regulated by cAMP. Cyclic AMP 123-127 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 8587236-2 1995 The objective of this study was to investigate the role of cAMP in the regulation of IL-6 and IL-8 gene expression and peptide production in IL-1 stimulated human MC. Cyclic AMP 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 8587236-9 1995 Taken together, our results demonstrate that cAMP differentially regulates IL-6 and IL-8 production in IL-1-stimulated human MC. Cyclic AMP 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 9053741-3 1995 Trifluoperazine, N-(6-aminohexyl)-5-chloro-1- naphthalenesulphonamide (W-7), fendiline and calmidazolium themselves had no effect on basal IP formation, but concentration-dependently (1-30 microM) potentiated ATP-, NaF- and A23187-stimulated IP formation. n-(6-aminohexyl)-5-chloro-1- naphthalenesulphonamide 17-69 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 7497463-3 1995 In this paper, data are summarized revealing the ability of WBH to induce elevated plasma levels of granulocyte-colony stimulating factor (G-CSF), interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10), and tumor necrosis factor-alpha (TNF-alpha) within hours of WBH. wbh 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 201-214 7497463-3 1995 In this paper, data are summarized revealing the ability of WBH to induce elevated plasma levels of granulocyte-colony stimulating factor (G-CSF), interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10), and tumor necrosis factor-alpha (TNF-alpha) within hours of WBH. wbh 60-63 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 8595612-3 1995 DESIGN: In a series of experiments, we examined the effect of heparin (4 U/ml) comparing it with ethylenediamine tetra-acetate (EDTA, 1.5 mg/ml) and citrate mixture (100 microliters/ml), heparin dose-response, IL8 (human recombinant IL8) dose-response and protamine (80 micrograms/ml) neutralisation of heparin (4 U/ml) using donor blood (total of 38). Heparin 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 210-213 8595612-3 1995 DESIGN: In a series of experiments, we examined the effect of heparin (4 U/ml) comparing it with ethylenediamine tetra-acetate (EDTA, 1.5 mg/ml) and citrate mixture (100 microliters/ml), heparin dose-response, IL8 (human recombinant IL8) dose-response and protamine (80 micrograms/ml) neutralisation of heparin (4 U/ml) using donor blood (total of 38). Heparin 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 233-236 7592725-8 1995 Thus, phosphatidic acid and lysophosphatidic acid, similarly to other physiological chemoattractants (e.g. C5a and interleukin-8), induce cell migration by an haptotactic mechanism. Phosphatidic Acids 6-23 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 7580291-3 1995 Histamine, but not PAF or endothelin-1, showed a dose-dependent stimulatory effect on the release of interleukin-6, interleukin-8 and granulocyte-macrophage colony-stimulating factor by normal and transformed human bronchial epithelial cells when studied 6 h after the treatment. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 7499684-6 1995 Allergen challenge after exposure to both air and NO2 significantly (p < 0.05) increased levels of MCT, but not MPO and IL-8 in the nasal lavage fluid. Nitrogen Dioxide 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 7594569-7 1995 The experiments presented here demonstrate that Fas Ag ligation alone led to production of IL-8 by colonic epithelial cells and represented another function mediated by Fas Ag in addition to apoptosis. ammonium ferrous sulfate 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 7578017-2 1995 This receptor (ET-IL-8RA) displayed functional properties similar to those of the native receptor in neutrophils in that exposure to IL-8 stimulated GTPase activity, phosphoinositide (PI) hydrolysis, intracellular calcium mobilization, and degranulation in a pertussis toxin (PTx) susceptible fashion. Calcium 214-221 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 7578017-5 1995 Staurosporine totally blocked PMA-induced phosphorylation but only partially inhibited IL-8-mediated phosphorylation. Staurosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 7586450-3 1995 We hypothesized that human endothelial cells deprived of oxygen would secrete IL-8, which might translate into elevated IL-8 production after cardiac ischemia. Oxygen 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 7586450-3 1995 We hypothesized that human endothelial cells deprived of oxygen would secrete IL-8, which might translate into elevated IL-8 production after cardiac ischemia. Oxygen 57-63 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 7592725-8 1995 Thus, phosphatidic acid and lysophosphatidic acid, similarly to other physiological chemoattractants (e.g. C5a and interleukin-8), induce cell migration by an haptotactic mechanism. lysophosphatidic acid 28-49 C-X-C motif chemokine ligand 8 Homo sapiens 115-128 7559482-9 1995 Examination of additional IL-8-based mutants in the colony formation assay, which centered on the perturbation of the amino-terminal "ELR" motif, resulted in the observation that the highly active IL-8 mutant required both aspartic acid at amino acid residue 4 and either glutamine or asparagine at residue 6. Aspartic Acid 223-236 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 7559482-9 1995 Examination of additional IL-8-based mutants in the colony formation assay, which centered on the perturbation of the amino-terminal "ELR" motif, resulted in the observation that the highly active IL-8 mutant required both aspartic acid at amino acid residue 4 and either glutamine or asparagine at residue 6. Glutamine 272-281 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 7559482-9 1995 Examination of additional IL-8-based mutants in the colony formation assay, which centered on the perturbation of the amino-terminal "ELR" motif, resulted in the observation that the highly active IL-8 mutant required both aspartic acid at amino acid residue 4 and either glutamine or asparagine at residue 6. Asparagine 285-295 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Calcitriol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 8634157-1 1995 PURPOSE: To evaluate the efficacy of a sodium fluoride (NaF)/silica/xylitol dentifrice compared with that of a positive control NaF/silica dentifrice on caries increments in school children over a 3-year period in an area without an optimal level of fluoride in the drinking water (mean level <0.1 ppm). Sodium Fluoride 39-54 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 8634157-1 1995 PURPOSE: To evaluate the efficacy of a sodium fluoride (NaF)/silica/xylitol dentifrice compared with that of a positive control NaF/silica dentifrice on caries increments in school children over a 3-year period in an area without an optimal level of fluoride in the drinking water (mean level <0.1 ppm). Fluorides 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 7575485-9 1995 Calyculin A also acted synergistically with IL-1 or TNF alpha to cause a 2-fold potentiation of IL-1- or TNF alpha-induced IL-8 mRNA and peptide and RANTES mRNA expression. calyculin A 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Phorbol Esters 169-182 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Phorbol Esters 169-182 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Tetradecanoylphorbol Acetate 184-187 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 7670094-8 1995 Calcitriol does not alter the expression of any of these mRNAs, and only the stimulation of IL-8 mRNA by sodium butyrate is recovered. Butyric Acid 105-120 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Calcitriol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Calcitriol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Tretinoin 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Tretinoin 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 8593446-0 1995 Effect of theophylline on the production of interleukin-1 beta, tumor necrosis factor-alpha, and interleukin-8 by human peripheral blood mononuclear cells. Theophylline 10-22 C-X-C motif chemokine ligand 8 Homo sapiens 97-110 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Tretinoin 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 8593446-7 1995 rhIL-1 beta induced IL-8 production in a dose-dependent manner at concentrations of 1-100 units/ml, and theophylline (particularly at concentrations of 50 and 100 micrograms/ml), increased IL-8 production in the presence of rhIL-1 beta. Theophylline 104-116 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Butyric Acid 26-41 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Butyric Acid 26-41 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Butyric Acid 26-41 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Tretinoin 127-129 C-X-C motif chemokine ligand 8 Homo sapiens 51-64 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Tretinoin 127-129 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 7489182-9 1995 Lexipafant treatment significantly reduced serum IL-8 (P = 0.038), and IL-6 declined on day 1. lexipafant 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 7670094-4 1995 Calcitriol, 9 cis-RA, and sodium butyrate increase interleukin-8 (IL-8) mRNA expression, and pretreatment with these agents or RA potentiates the stimulation of IL-8 by phorbol ester (TPA). Tretinoin 127-129 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 7489942-0 1995 Interleukin 8 secretion by colonic crypt cells in vitro: response to injury suppressed by butyrate and enhanced in inflammatory bowel disease. Butyrates 90-98 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 7556959-5 1995 Transcapillary diffusion of sodium fluorescein (NaF) was quantitated by video densitometry in the skin in all subjects on the 4th treatment day. Fluorescein 28-46 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 7557080-8 1995 The chemokines IL-8 and IL-10, but not RANTES, increased [Ca2+]i in intraepithelial lymphocytes; this calcium mobilization was not affected by ethylene glycol-bis(beta-aminoethyl ether)-N,N,N",N"-tetraacetic acid, indicating that calcium is released from intracellular sources. Calcium 102-109 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 7557080-8 1995 The chemokines IL-8 and IL-10, but not RANTES, increased [Ca2+]i in intraepithelial lymphocytes; this calcium mobilization was not affected by ethylene glycol-bis(beta-aminoethyl ether)-N,N,N",N"-tetraacetic acid, indicating that calcium is released from intracellular sources. Calcium 230-237 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 7558346-2 1995 The aim of our study was to investigate whether MC are able to produce IL-8 after direct stimulation with clinically relevant bacteria. Methylcholanthrene 48-50 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 7558346-3 1995 We observed a significant IL-8 response by the MC which were directly stimulated with viable staphylococci. Methylcholanthrene 47-49 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 7559807-6 1995 Phosphorylation may not act directly on latent transcription factors, since bromophenacyl bromide, an inhibitor for the release of arachidonic acid from phorbol-12 myristate 13-acetate (PMA)-stimulated HL 60 cells, markedly depressed the induced mRNAs for IL-8, TNF-alpha, and IL-1 alpha and -beta. Tetradecanoylphorbol Acetate 186-189 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 7559807-0 1995 Inhibition of the arachidonic acid pathway prevents induction of IL-8 mRNA by phorbol ester and changes the release of IL-8 from HL 60 cells: differential inhibition of induced expression of IL-8, TNF-alpha, IL-1 alpha, and IL-1 beta. Arachidonic Acid 18-34 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 7559807-0 1995 Inhibition of the arachidonic acid pathway prevents induction of IL-8 mRNA by phorbol ester and changes the release of IL-8 from HL 60 cells: differential inhibition of induced expression of IL-8, TNF-alpha, IL-1 alpha, and IL-1 beta. Arachidonic Acid 18-34 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 8543371-6 1995 Pretreatment of neutrophils with the serine protease inhibitors PMSF or 3,4-DCI significantly reduced chemotaxis to C5a, fMLP and IL-8. Phenylmethylsulfonyl Fluoride 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 8543371-6 1995 Pretreatment of neutrophils with the serine protease inhibitors PMSF or 3,4-DCI significantly reduced chemotaxis to C5a, fMLP and IL-8. 3,4-dichloroisocoumarin 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 7560091-5 1995 NECA 10 microM evoked IL-8 release from HMC-1, but CGS21680 10 microM had no effect. Adenosine-5'-(N-ethylcarboxamide) 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 7559807-0 1995 Inhibition of the arachidonic acid pathway prevents induction of IL-8 mRNA by phorbol ester and changes the release of IL-8 from HL 60 cells: differential inhibition of induced expression of IL-8, TNF-alpha, IL-1 alpha, and IL-1 beta. Arachidonic Acid 18-34 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 7559807-0 1995 Inhibition of the arachidonic acid pathway prevents induction of IL-8 mRNA by phorbol ester and changes the release of IL-8 from HL 60 cells: differential inhibition of induced expression of IL-8, TNF-alpha, IL-1 alpha, and IL-1 beta. Phorbol Esters 78-91 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 7559807-6 1995 Phosphorylation may not act directly on latent transcription factors, since bromophenacyl bromide, an inhibitor for the release of arachidonic acid from phorbol-12 myristate 13-acetate (PMA)-stimulated HL 60 cells, markedly depressed the induced mRNAs for IL-8, TNF-alpha, and IL-1 alpha and -beta. 4-bromophenacyl bromide 76-97 C-X-C motif chemokine ligand 8 Homo sapiens 256-260 7560091-7 1995 Both theophylline and enprofylline 300 micro completely blocked the release of IL-8 by NECA. Theophylline 5-17 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 7559807-8 1995 In contrast, ETYA increased the induced IL-8 RNA levels and stimulated the release for IL-8. ETYA 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 7560091-7 1995 Both theophylline and enprofylline 300 micro completely blocked the release of IL-8 by NECA. enprofylline 22-34 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 7559807-8 1995 In contrast, ETYA increased the induced IL-8 RNA levels and stimulated the release for IL-8. ETYA 13-17 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 7559807-10 1995 However, the release of IL-8 protein was regulated by indomethacin and ketoconazole. Indomethacin 54-66 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 7559807-10 1995 However, the release of IL-8 protein was regulated by indomethacin and ketoconazole. Ketoconazole 71-83 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 7559807-11 1995 Our results indicate that arachidonic acid metabolites are mediators in the signal transduction pathway of IL-8 expression and that the involved second messengers are different from those which are important for the induction of TNF-alpha and IL-1 beta expression. Arachidonic Acid 26-42 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 8845742-4 1995 in the human microglia cells ammonia decreased the constitutive secretion of interleukin-6, but it enhanced the stimulated (interleukin-1 alpha, tumor necrosis factor-alpha, gamma-interferon and gamma-interferon + tumor necrosis factor-alpha) secretion of interleukin-8. Ammonia 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 256-269 8576944-3 1995 Here we demonstrate that the four Ca(2+)-channel blockers, Amlodipine, Felodipine, Isradipine and Manidipine, at nanomolar concentrations, activate the transcription of the genes encoding IL-6 and IL-8 in primary human VSMC and fibroblasts. Amlodipine 59-69 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 8576944-3 1995 Here we demonstrate that the four Ca(2+)-channel blockers, Amlodipine, Felodipine, Isradipine and Manidipine, at nanomolar concentrations, activate the transcription of the genes encoding IL-6 and IL-8 in primary human VSMC and fibroblasts. Felodipine 71-81 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 8576944-3 1995 Here we demonstrate that the four Ca(2+)-channel blockers, Amlodipine, Felodipine, Isradipine and Manidipine, at nanomolar concentrations, activate the transcription of the genes encoding IL-6 and IL-8 in primary human VSMC and fibroblasts. Isradipine 83-93 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 8576944-3 1995 Here we demonstrate that the four Ca(2+)-channel blockers, Amlodipine, Felodipine, Isradipine and Manidipine, at nanomolar concentrations, activate the transcription of the genes encoding IL-6 and IL-8 in primary human VSMC and fibroblasts. manidipine 98-108 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 8845742-5 1995 In the astroglioma cell line, the stimulated release of tumor necrosis factor-alpha, interleukin-6 and interleukin-8 was diminished by ammonium acetate. ammonium acetate 135-151 C-X-C motif chemokine ligand 8 Homo sapiens 103-116 7575568-0 1995 Nitric oxide regulates IL-8 expression in melanoma cells at the transcriptional level. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 7575568-1 1995 We investigated the role of nitric oxide (NO) in the expression of interleukin-8 (IL-8) in the human melanoma cell line, G361. Nitric Oxide 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 7575568-1 1995 We investigated the role of nitric oxide (NO) in the expression of interleukin-8 (IL-8) in the human melanoma cell line, G361. Nitric Oxide 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 7575682-4 1995 Whereas migration by formyl-methionyl-leucyl-phenylalanine (fMLP)- or interleukin-8-activated electroporated neutrophils was strongly inhibited by ryanodine, chemotaxis induced by protein kinase C activators was not affected. Ryanodine 147-156 C-X-C motif chemokine ligand 8 Homo sapiens 70-83 7575568-5 1995 The nitric oxide synthase inhibitor, NG-amino-L-homoarginine (NAHA), inhibited TNF-alpha-stimulated IL-8 promoter activity by 60%. Nitric Oxide 4-16 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 7575568-5 1995 The nitric oxide synthase inhibitor, NG-amino-L-homoarginine (NAHA), inhibited TNF-alpha-stimulated IL-8 promoter activity by 60%. ng-amino-l-homoarginine 37-60 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 7575568-5 1995 The nitric oxide synthase inhibitor, NG-amino-L-homoarginine (NAHA), inhibited TNF-alpha-stimulated IL-8 promoter activity by 60%. naha 62-66 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 7486675-0 1995 IL-8 induces calcium mobilization in interleukin-2-activated natural killer cells independently of inositol 1,4,5 trisphosphate. Calcium 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8549642-5 1995 Consistent with the effects on endothelin and ATP, NaF-induced inositol phosphate formation was also inhibited by cAMP generating agents to a similar extent. Adenosine Triphosphate 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 8549642-5 1995 Consistent with the effects on endothelin and ATP, NaF-induced inositol phosphate formation was also inhibited by cAMP generating agents to a similar extent. Inositol Phosphates 63-81 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 8549642-5 1995 Consistent with the effects on endothelin and ATP, NaF-induced inositol phosphate formation was also inhibited by cAMP generating agents to a similar extent. Cyclic AMP 114-118 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 7545393-5 1995 We show that pyrrolidine dithiocarbamate strongly reduces the TNF alpha-mediated induction of E-selectin, VCAM-1, ICAM-1, PAI-1, tissue factor, IL-8 and I kappa B-alpha. pyrrolidine dithiocarbamic acid 13-40 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 7677475-3 1995 METHODS: This initial study evaluated the impact of heparin-bonded CPB circuits on production of the cytokines interleukin-1 (IL-1), tumor necrosis factor-alpha (TNF-a), IL-6, and IL-8 in adults undergoing complex cardiac operations with prolonged CPB. Heparin 52-59 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 7677475-6 1995 RESULTS: The levels of IL-6 and IL-8 increased in a time-dependent fashion in both groups, but the response was significantly less over time in the heparin-bonded group (p < 0.05) for both IL-6 and IL-8. Heparin 148-155 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 8846658-1 1995 Sodium Fluoride (NaF) is the only medication so far clinically available with a bone formation stimulating property, through its peculiar mitogenic dose-dependent action on the osteoblast cell line. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 7669585-4 1995 Histological examination of the site of injection of CHO clones transfected with hu-IL-8, hu-MIP-1 alpha or mu-MIP-1 alpha showed predominantly neutrophilic infiltration. cho 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 8846658-7 1995 Third, if one wants to avoid a calcium shift from cortical to trabecular bone and osteomalacia, one should use small doses of NaF, of the order of 50 mg/day. Calcium 31-38 C-X-C motif chemokine ligand 8 Homo sapiens 126-129 11540313-4 1995 A new treatment program entailing intermittent slow release sodium fluoride (SR-NaF) with continuous calcium citrate may capture desirable qualities of fluoride without toxic effects, and be therapeutically efficacious in postmenopausal osteoporosis. Sodium Fluoride 60-75 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 8575568-5 1995 Incubation of the epithelial cultures in the presence of 0.1-10 micrograms.mL-1 erythromycin significantly blocked the HIE-induced release of IL-6, IL-8, and sICAM-1, at all concentrations of erythromycin investigated. Erythromycin 80-92 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 8523463-4 1995 CINC is a rat equivalent of human interleukin-8. Zinc 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 7642293-5 1995 The synthesis of IL-6 and IL-8 was also stimulated by 10 and 100 micrograms of both LPSs per ml, but IL-8 synthesis was not stimulated with E-LPS at 1 microgram/ml. lpss 84-88 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 7642293-6 1995 Secretion of IL-6 and IL-8 into the culture medium was detected at 6 and 3 h, respectively, after exposure to P-LPS (10 micrograms/ml). p-lps 110-115 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 7657801-8 1995 A second mechanism for trophozoite-induced IL-8 production involves trophozoite-target cell contact via a galactose-inhibitable amebic adherence protein, and appears to be mediated through increased intracellular calcium levels. Galactose 106-115 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 7657801-8 1995 A second mechanism for trophozoite-induced IL-8 production involves trophozoite-target cell contact via a galactose-inhibitable amebic adherence protein, and appears to be mediated through increased intracellular calcium levels. Calcium 213-220 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 7594798-5 1995 After treatment with macrolide antibiotics, significant reductions in the concentrations of defensins, IL-8 and neutrophil numbers in BALF of DPB patients were observed. Macrolides 21-30 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 11540313-4 1995 A new treatment program entailing intermittent slow release sodium fluoride (SR-NaF) with continuous calcium citrate may capture desirable qualities of fluoride without toxic effects, and be therapeutically efficacious in postmenopausal osteoporosis. Calcium Citrate 101-116 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 11540313-4 1995 A new treatment program entailing intermittent slow release sodium fluoride (SR-NaF) with continuous calcium citrate may capture desirable qualities of fluoride without toxic effects, and be therapeutically efficacious in postmenopausal osteoporosis. Fluorides 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 7576392-9 1995 The polyampholyte-NaF delivery system with 1100 ppm F- was equivalent to the 2800 ppm F- dentifrice. polyampholyte 4-17 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 7543020-5 1995 Induction of IL-8 was UV-B dose dependent and blocked by cyclohexamide, indicating that de novo protein synthesis is required for its expression. 4-[2-(3,5-dimethyl-2-oxocyclohexyl)-2-hydroxyethyl]piperidine-2,6-dione 57-70 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 7487568-1 1995 Fluoride-mediated inhibition of peroxidase potential activity in human saliva was investigated using NaF, NH4F, CaF2, Na2PO3F (MFP), SnF2 and TiF4. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 7543732-5 1995 Apigenin also inhibited IL-1 alpha-induced prostaglandin synthesis and TNF-alpha-induced IL-6 and IL-8 production, suggesting that the hydroxyflavones may act as general inhibitors of cytokine-induced gene expression. hydroxyflavones 135-150 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 7626291-9 1995 We did, however, demonstrate a dose-dependent decrease in IL-8 release and IL-8 mRNA induction in RSV-infected epithelial treated with the antioxidants dimethyl sulfoxide (DMSO) or 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). Dimethyl Sulfoxide 152-170 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 7626291-9 1995 We did, however, demonstrate a dose-dependent decrease in IL-8 release and IL-8 mRNA induction in RSV-infected epithelial treated with the antioxidants dimethyl sulfoxide (DMSO) or 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). Dimethyl Sulfoxide 152-170 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 7626291-9 1995 We did, however, demonstrate a dose-dependent decrease in IL-8 release and IL-8 mRNA induction in RSV-infected epithelial treated with the antioxidants dimethyl sulfoxide (DMSO) or 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). Dimethyl Sulfoxide 172-176 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 7626291-9 1995 We did, however, demonstrate a dose-dependent decrease in IL-8 release and IL-8 mRNA induction in RSV-infected epithelial treated with the antioxidants dimethyl sulfoxide (DMSO) or 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). Dimethyl Sulfoxide 172-176 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 7626291-9 1995 We did, however, demonstrate a dose-dependent decrease in IL-8 release and IL-8 mRNA induction in RSV-infected epithelial treated with the antioxidants dimethyl sulfoxide (DMSO) or 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). 5,5-dimethyl-1-pyrroline-1-oxide 181-213 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 7626291-9 1995 We did, however, demonstrate a dose-dependent decrease in IL-8 release and IL-8 mRNA induction in RSV-infected epithelial treated with the antioxidants dimethyl sulfoxide (DMSO) or 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). 5,5-dimethyl-1-pyrroline-1-oxide 181-213 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 7626291-9 1995 We did, however, demonstrate a dose-dependent decrease in IL-8 release and IL-8 mRNA induction in RSV-infected epithelial treated with the antioxidants dimethyl sulfoxide (DMSO) or 5,5-dimethyl-1-pyrroline-N-oxide (DMPO). 5,5-dimethyl-1-pyrroline-1-oxide 215-219 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 7487568-2 1995 At pH 5.5 and for a 20 mM F concentration, the inhibition percentages increased from 2% for MFP and 5% for CaF2 to 61% for NaF and 65% for NH4F, while a 100% inhibition was observed at 10 mM for TiF4 and at 5 mM for SnF2. Fluorine 26-27 C-X-C motif chemokine ligand 8 Homo sapiens 123-126 8546810-9 1995 Addition of TSH (1 mU/ml) produced an increase in the level of IL-1 alpha mRNA in primary TFC and HTori3 cells, at 12 and 24 h. TSH had no significant effect on the expression of IL-6 or IL-8 mRNA. Thyrotropin 12-15 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 8528601-0 1995 Pharmacological modulation of IL-6 and IL-8 secretion by the H1-antagonist decarboethoxy-loratadine and dexamethasone by human mast and basophilic cell lines. decarboethoxy-loratadine 75-99 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 7622884-6 1995 Interleukin-8 (IL-8) and leukotriene B4 (LTB4) were released in greater quantities by adult monocytes in response to either GBS or lipopolysaccharide. gbs 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 7622884-6 1995 Interleukin-8 (IL-8) and leukotriene B4 (LTB4) were released in greater quantities by adult monocytes in response to either GBS or lipopolysaccharide. gbs 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 7622884-9 1995 IL-8 and LTB4 accounted for the majority of chemoattractant activity released in response to GBS. gbs 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7622884-10 1995 Decreased production of LTB4 and IL-8 may contribute to the neonate"s poor host response to GBS. gbs 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 8570304-6 1995 Proinflammatory cytokines and proteinases were generally elevated, and interleukin-8 (IL-8) concentration correlated inversely with oxygen saturation (SaO2). Oxygen 132-138 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 8570304-6 1995 Proinflammatory cytokines and proteinases were generally elevated, and interleukin-8 (IL-8) concentration correlated inversely with oxygen saturation (SaO2). Oxygen 132-138 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 8570304-6 1995 Proinflammatory cytokines and proteinases were generally elevated, and interleukin-8 (IL-8) concentration correlated inversely with oxygen saturation (SaO2). sao2 151-155 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 8570304-6 1995 Proinflammatory cytokines and proteinases were generally elevated, and interleukin-8 (IL-8) concentration correlated inversely with oxygen saturation (SaO2). sao2 151-155 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 7546131-6 1995 Results of studies have varied, but the largest ever double-blind NaF/SMFP head-to-head dentifrice trial yet published (Stephen et al., 1994) has indicated a 6.4% significant benefit in favor of NaF (in silica) over SMFP. Silicon Dioxide 203-209 C-X-C motif chemokine ligand 8 Homo sapiens 195-198 7546131-8 1995 In relation to root caries, Jensen and Kohout (1988) reported a 41.4% DFS significant reduction in subjects who used a NaF/silica dentifrice at 1100 ppm F, over a one-year period. Silicon Dioxide 123-129 C-X-C motif chemokine ligand 8 Homo sapiens 119-122 7677428-5 1995 Patients who had high blood levels of pentachlorophenol and abnormal lymphocyte stimulation also had increased proportions of blood monocytes in blood (p < .05), as well as increased IL-8 serum levels (p < .02). Pentachlorophenol 38-55 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 7555210-0 1995 Cefodizime modulates in vitro tumor necrosis factor-alpha, interleukin-6 and interleukin-8 release from human peripheral monocytes. cefodizime 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 7670776-2 1995 Significant stimulation of IL-1ra and sTNFR p75 as well as inhibition of IL-8 production of PBMC were associated with clinical improvement observed in patients treated with MTX. Methotrexate 173-176 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 7789553-6 1995 A significant positive correlation was observed between the levels of reactive oxygen species and IL-8. Reactive Oxygen Species 70-93 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 7540987-0 1995 Upregulation of interleukin-8 receptor in human polymorphonuclear neutrophils by formyl peptide and lipopolysaccharide. formyl peptide 81-95 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 7577839-4 1995 IL-8 production in PBMC was closely related to the clinical severity of psoriasis and to the response to treatment, including systemic methotrexate (MTX) treatment and tonsillectomy. Methotrexate 135-147 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7577839-4 1995 IL-8 production in PBMC was closely related to the clinical severity of psoriasis and to the response to treatment, including systemic methotrexate (MTX) treatment and tonsillectomy. Methotrexate 149-152 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7615975-4 1995 Transforming growth factor (TGF)-alpha, epidermal growth factor, and phorbol myristate acetate also enhanced the secretion of VPF/VEGF by keratinocytes; in contrast, a number of other cytokines including interleukin (IL)-1, IL-6, IL-8, tumor necrosis factor-alpha, interferon-gamma, and transforming growth factor-beta did not induce VPF/VEGF secretion. Tetradecanoylphorbol Acetate 69-94 C-X-C motif chemokine ligand 8 Homo sapiens 230-234 7637390-1 1995 Interleukin-8 (IL-8) mRNA was rapidly, but not permanently, induced at high levels by phorbol-12myristate-13acetate (PMA) in HL60 cells. Tetradecanoylphorbol Acetate 86-115 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 7637390-1 1995 Interleukin-8 (IL-8) mRNA was rapidly, but not permanently, induced at high levels by phorbol-12myristate-13acetate (PMA) in HL60 cells. Tetradecanoylphorbol Acetate 86-115 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 7637390-1 1995 Interleukin-8 (IL-8) mRNA was rapidly, but not permanently, induced at high levels by phorbol-12myristate-13acetate (PMA) in HL60 cells. Tetradecanoylphorbol Acetate 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 7637390-1 1995 Interleukin-8 (IL-8) mRNA was rapidly, but not permanently, induced at high levels by phorbol-12myristate-13acetate (PMA) in HL60 cells. Tetradecanoylphorbol Acetate 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 7637390-3 1995 However, the rate of transient induction kinetics was modulated by cycloheximide (CHX) indicating that secondary response genes are involved in the regulation of IL-8 RNA levels. Cycloheximide 67-80 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 7637390-3 1995 However, the rate of transient induction kinetics was modulated by cycloheximide (CHX) indicating that secondary response genes are involved in the regulation of IL-8 RNA levels. Cycloheximide 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 7794282-0 1995 Nitric oxide regulation of IL-8 expression in human endothelial cells. Nitric Oxide 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 7794282-2 1995 We examined the role of nitric oxide (NO) in IL-8 regulation. Nitric Oxide 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 7794282-3 1995 The NO synthase inhibitor, (L)-NG-nitroarginine methyl ester (L-NAME), inhibited the TNF-stimulated IL-8 production in the human endothelial cell line, ECV304, in a dose-dependent manner without affecting cellular viability (TNF alone, 5.5 +/- 0.9 ng/ml; TNF + 5 mM L-NAME, 2.4 +/- 0.5 ng/ml). (l)-ng-nitroarginine methyl ester 27-60 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 7794282-3 1995 The NO synthase inhibitor, (L)-NG-nitroarginine methyl ester (L-NAME), inhibited the TNF-stimulated IL-8 production in the human endothelial cell line, ECV304, in a dose-dependent manner without affecting cellular viability (TNF alone, 5.5 +/- 0.9 ng/ml; TNF + 5 mM L-NAME, 2.4 +/- 0.5 ng/ml). NG-Nitroarginine Methyl Ester 62-68 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 7794282-4 1995 Moreover, exogenously added NO produced by the spontaneous NO generating compounds, S-Nitroso-N-acetyl-D,L-pennicillamine (SNAP) and Ethanamine, 2,2"-(hydroxynitrosohydrazono)bis- (DETA NONOate), induced a dose-dependent release of IL-8 from these cells. s-nitroso-n-acetyl-d,l-pennicillamine 84-121 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 7794282-4 1995 Moreover, exogenously added NO produced by the spontaneous NO generating compounds, S-Nitroso-N-acetyl-D,L-pennicillamine (SNAP) and Ethanamine, 2,2"-(hydroxynitrosohydrazono)bis- (DETA NONOate), induced a dose-dependent release of IL-8 from these cells. 2,2"-(hydroxynitrosohydrazono)bis- (deta nonoate 145-193 C-X-C motif chemokine ligand 8 Homo sapiens 232-236 7794282-5 1995 Maximal stimulation of IL-8 was found to be 1.2 +/- 0.1 ng/ml with the 1 mM concentration of SNAP and 1.6 +/- 0.1 ng/ml with the 2 mM concentration of DETA NONOate. 2,2'-(hydroxynitrosohydrazono)bis-ethanamine 151-163 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 7759889-0 1995 Increased cell-associated IL-8 in human exudative and A23187-treated peripheral blood neutrophils. Calcimycin 54-60 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 7759889-5 1995 Furthermore, cell-associated IL-8 in peripheral blood neutrophils increased 20-fold during incubation at 37 degrees C in vitro and was increased over 200-fold after treatment with the Ca2+ ionophore A23187. Calcimycin 199-205 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 7737976-2 1995 This study defines an important region between Cys7 and Cys50 that, together with the Glu4-Leu5-Arg6 sequence of the NH2 terminus, accounts for the high affinity binding of IL-8 to the IL-8 A receptor on leukocytes. CYS7 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 7759889-6 1995 More than 35% of the cell-associated IL-8 could be released by stimulation with either Ca2+ ionophore A23187 or phorbol myristate acetate. Calcimycin 102-108 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 7759889-6 1995 More than 35% of the cell-associated IL-8 could be released by stimulation with either Ca2+ ionophore A23187 or phorbol myristate acetate. Tetradecanoylphorbol Acetate 112-137 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 7759889-7 1995 IL-8 was localized by sucrose gradient centrifugation to a subcellular fraction of heterogeneous, light membranous organelles. Sucrose 22-29 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7759889-8 1995 The accumulation of IL-8 within these organelles is inhibited by cycloheximide but not actinomycin D, suggesting that IL-8 accumulation is under translational, rather than transcriptional control. Cycloheximide 65-78 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 7759889-8 1995 The accumulation of IL-8 within these organelles is inhibited by cycloheximide but not actinomycin D, suggesting that IL-8 accumulation is under translational, rather than transcriptional control. Cycloheximide 65-78 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 7590784-9 1995 Similarly, a 300-fold molar excess of anti-IL-8 antibody [10(-5) M] was necessary to abrogate the increase in cytosolic free calcium in neutrophils stimulated with 4 x 10(-8) M rhIL-8. Calcium 125-132 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 7590896-3 1995 Oxyradical production is one of the lytic mechanisms used by phagocytes, and IL-8 is shown to activate this function, which does not occur if neutrophils are pretreated with the protein kinase C inhibitor, staurosporine, but is increased by R59022, a dyacylglycerol kinase inhibitor. Staurosporine 206-219 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 7590896-3 1995 Oxyradical production is one of the lytic mechanisms used by phagocytes, and IL-8 is shown to activate this function, which does not occur if neutrophils are pretreated with the protein kinase C inhibitor, staurosporine, but is increased by R59022, a dyacylglycerol kinase inhibitor. R 59022 241-247 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 7590896-4 1995 The IL-8 effect is mediated by protein kinase C, which is potentiated by the calcium flux induced by the interaction between antibody coating tumour target and Fc gamma RIII on effector cells, as previously demonstrated. Calcium 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 7790770-6 1995 However, neutrophils pretreated with interleukin-8 ingested IgA-opsonized microspheres and released superoxide when exposed to IgA antibody-antigen complexes. Superoxides 100-110 C-X-C motif chemokine ligand 8 Homo sapiens 37-50 7763262-0 1995 Regulation of interleukin-8 gene expression by all-trans retinoic acid. Tretinoin 57-70 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 7763262-1 1995 We have studied the relationship between interleukin-8 (IL-8) and interleukin-1 alpha (IL-1 alpha) release after stimulation with all-trans retinoic acid (ATRA) and tumor necrosis factor-alpha (TNF-alpha) in the human epithelial ovarian cancer cell line HOC-7. Tretinoin 140-153 C-X-C motif chemokine ligand 8 Homo sapiens 41-54 7763262-1 1995 We have studied the relationship between interleukin-8 (IL-8) and interleukin-1 alpha (IL-1 alpha) release after stimulation with all-trans retinoic acid (ATRA) and tumor necrosis factor-alpha (TNF-alpha) in the human epithelial ovarian cancer cell line HOC-7. Tretinoin 140-153 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 7763262-1 1995 We have studied the relationship between interleukin-8 (IL-8) and interleukin-1 alpha (IL-1 alpha) release after stimulation with all-trans retinoic acid (ATRA) and tumor necrosis factor-alpha (TNF-alpha) in the human epithelial ovarian cancer cell line HOC-7. Tretinoin 155-159 C-X-C motif chemokine ligand 8 Homo sapiens 41-54 7763262-1 1995 We have studied the relationship between interleukin-8 (IL-8) and interleukin-1 alpha (IL-1 alpha) release after stimulation with all-trans retinoic acid (ATRA) and tumor necrosis factor-alpha (TNF-alpha) in the human epithelial ovarian cancer cell line HOC-7. Tretinoin 155-159 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 7763262-2 1995 Both IL-1 alpha and IL-8 protein release were enhanced by treatment with ATRA and TNF-alpha after 48 h exposure. Tretinoin 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 7763262-3 1995 Blocking of IL-1 alpha activity in HOC-7 cells with either IL-1 receptor antagonist (IL-1ra) or a neutralizing antibody directed against IL-1 alpha resulted in a dose-dependent decrease of IL-8 release by ATRA, TNF-alpha and IL-1 alpha treated HOC-7 cells. Tretinoin 205-209 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 7737976-2 1995 This study defines an important region between Cys7 and Cys50 that, together with the Glu4-Leu5-Arg6 sequence of the NH2 terminus, accounts for the high affinity binding of IL-8 to the IL-8 A receptor on leukocytes. CYS7 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 8589272-2 1995 Upon granulocytic differentiation with all-trans retinoic acid (ATRA) or the combination of ATRA and granulocyte-colony-stimulating factor (G-CSF), significant amounts of IL-1 beta and IL-8 mRNAs accumulated in both cell types. Tretinoin 49-62 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 7614647-0 1995 Methylprednisolone inhibits increase of interleukin 8 and 6 during open heart surgery. Methylprednisolone 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 7614647-3 1995 This prospective study was conducted to investigate whether methylprednisolone (MP) pretreatment (30 mg.kg-1 before CPB and before declamping of aorta) influenced the production of IL-8 and 6 in the peripheral circulation in 27 patients undergoing elective coronary artery bypass surgery. Methylprednisolone 60-78 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 7614647-3 1995 This prospective study was conducted to investigate whether methylprednisolone (MP) pretreatment (30 mg.kg-1 before CPB and before declamping of aorta) influenced the production of IL-8 and 6 in the peripheral circulation in 27 patients undergoing elective coronary artery bypass surgery. Methylprednisolone 80-82 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 8589272-2 1995 Upon granulocytic differentiation with all-trans retinoic acid (ATRA) or the combination of ATRA and granulocyte-colony-stimulating factor (G-CSF), significant amounts of IL-1 beta and IL-8 mRNAs accumulated in both cell types. Tretinoin 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 7738357-0 1995 Interleukin-8 and GRO alpha prime human neutrophils for superoxide anion production and induce up-regulation of N-formyl peptide receptors. Superoxides 56-72 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 7539029-9 1995 It is interesting that the major structural difference between IL-8 and PF4 is the presence of the NH2-terminal ELR (Glu-Leu-Arg) motif that precedes the first cysteine amino acid residue of IL-8 and is important in ligand/receptor interactions. Glutamic Acid 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7539029-9 1995 It is interesting that the major structural difference between IL-8 and PF4 is the presence of the NH2-terminal ELR (Glu-Leu-Arg) motif that precedes the first cysteine amino acid residue of IL-8 and is important in ligand/receptor interactions. leucylarginine 121-128 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7539029-9 1995 It is interesting that the major structural difference between IL-8 and PF4 is the presence of the NH2-terminal ELR (Glu-Leu-Arg) motif that precedes the first cysteine amino acid residue of IL-8 and is important in ligand/receptor interactions. cysteine amino acid 160-179 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7539029-9 1995 It is interesting that the major structural difference between IL-8 and PF4 is the presence of the NH2-terminal ELR (Glu-Leu-Arg) motif that precedes the first cysteine amino acid residue of IL-8 and is important in ligand/receptor interactions. cysteine amino acid 160-179 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 7542063-3 1995 IL-4, but not SCF, enhanced ionomycin-induced transcription and secretion of several genes, including the cytokines IL-3, IL-4, granulocyte/macrophage-colony-stimulating factor, IL-8 and the receptor for IL-6 in the human HMC-1 mast cell line. Ionomycin 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 7542097-0 1995 Expression of granulocyte/macrophage-colony-stimulating factor, interleukin-8 and RANTES in the bronchial epithelium of mild asthmatics is down-regulated by inhaled beclomethasone dipropionate. Beclomethasone 165-192 C-X-C motif chemokine ligand 8 Homo sapiens 64-77 7722453-6 1995 By this measure, IL-8- or LTB4-treated PMN adhered loosely to fibrin, since 10 kD rhodamine-polyethylene glycol permeated into the contact zones between these cells and the underlying fibrin gel. rhodamine-polyethylene glycol 82-111 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 7722453-7 1995 PMN stimulated with FMLP and IL-8, or FMLP and LTB4, exhibited very little migration through fibrin gels, and three times as many of these cells excluded 10 kD rhodamine-polyethylene glycol from their zones of contact with fibrin as PMN stimulated with IL-8 or LTB4 alone. rhodamine-polyethylene glycol 160-189 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 7722326-9 1995 The MBP-stimulated production of IL-8 was inhibited by actinomycin D, but not by cyclosporin A. Dactinomycin 55-68 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 7738357-3 1995 IL-8 and GRO alpha themselves did not stimulate production of significant amounts of superoxide anions but potentiated N-formyl peptide-induced superoxide anion production in a concentration-dependent manner. n-formyl peptide 119-135 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7738357-4 1995 Binding measurements by flow cytometry at 37 degrees C with fluorescein-labeled N-formyl peptide revealed enhanced total N-formyl peptide binding after pretreatment of neutrophils with IL-8 and GRO alpha. Fluorescein 60-71 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 7738357-4 1995 Binding measurements by flow cytometry at 37 degrees C with fluorescein-labeled N-formyl peptide revealed enhanced total N-formyl peptide binding after pretreatment of neutrophils with IL-8 and GRO alpha. n-formyl peptide 80-96 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 7738357-4 1995 Binding measurements by flow cytometry at 37 degrees C with fluorescein-labeled N-formyl peptide revealed enhanced total N-formyl peptide binding after pretreatment of neutrophils with IL-8 and GRO alpha. n-formyl peptide 121-137 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 7738357-6 1995 This study indicates that IL-8 and GRO alpha, in addition to their known chemotactic activity, prime neutrophils for superoxide anion production, presumably by up-regulating the number of receptors for strong superoxide-anion-triggering stimuli. Superoxides 117-133 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 7738357-6 1995 This study indicates that IL-8 and GRO alpha, in addition to their known chemotactic activity, prime neutrophils for superoxide anion production, presumably by up-regulating the number of receptors for strong superoxide-anion-triggering stimuli. Superoxides 209-225 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 7740640-1 1995 In order to evaluate the effect of sodium fluoride (NaF) on bone biomechanical competence, iliac crest biopsies were taken before and after one year of treatment in 12 osteoporotic patients, and before and after five years of treatment in 14 patients. Sodium Fluoride 35-50 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 7706709-4 1995 Stimulation of T lymphocytes or T cell clones with IL-8 led to generation of inositol trisphosphate and calcium flux. inositol 1,2,3-trisphosphate 77-99 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 7706709-4 1995 Stimulation of T lymphocytes or T cell clones with IL-8 led to generation of inositol trisphosphate and calcium flux. Calcium 104-111 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 7706709-5 1995 In addition, when T cells were prelabeled with [3H]oleic acid, IL-8 caused a long lasting, time- and dose-related increase in [3H]phosphatidylethanol (PtE), indicating activation of phospholipase D (PLD). [3h]oleic acid 47-61 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7706709-5 1995 In addition, when T cells were prelabeled with [3H]oleic acid, IL-8 caused a long lasting, time- and dose-related increase in [3H]phosphatidylethanol (PtE), indicating activation of phospholipase D (PLD). [3h]phosphatidylethanol 126-149 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7706709-5 1995 In addition, when T cells were prelabeled with [3H]oleic acid, IL-8 caused a long lasting, time- and dose-related increase in [3H]phosphatidylethanol (PtE), indicating activation of phospholipase D (PLD). pte 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7535813-6 1995 Staurosporine inhibits freshly isolated T lymphocyte chemotaxis toward IL-8, whereas tyrphostin 23 inhibits chemotaxis of overnight cultured and anti-CD3-activated T lymphocytes toward IL-1 alpha. Staurosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 7615691-4 1995 Pretreatment of polymorphonuclear leucocytes with 50 microM BAPTA/AM, an intracellular calcium chelator, lowered the basal level in cell calcium and inhibited the transient calcium rise stimulated by 2 nM interleukin-8, 2 nM C5a, and 10 nM N-formylmethionyl-leucyl-phenylalanine. N-Formylmethionine Leucyl-Phenylalanine 240-278 C-X-C motif chemokine ligand 8 Homo sapiens 205-218 7751024-3 1995 Stimulation of non-IL-4-treated cells with ionomycin (10 microM) for periods of 30 min to 8 hr induced expression of mRNA encoding IL-3, IL-4 and IL-8 but was without effect on levels of mRNA for tumour necrosis factor (TNF)-alpha or beta-actin. Ionomycin 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 7615691-1 1995 Chemoattractants such as interleukin-8, C5a and N-formylmethionyl-leucyl-phenylalanine induce a cytosolic calcium rise involved in triggering the secretory functions of human polymorphonuclear leucocytes. Calcium 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 25-38 7615691-4 1995 Pretreatment of polymorphonuclear leucocytes with 50 microM BAPTA/AM, an intracellular calcium chelator, lowered the basal level in cell calcium and inhibited the transient calcium rise stimulated by 2 nM interleukin-8, 2 nM C5a, and 10 nM N-formylmethionyl-leucyl-phenylalanine. 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid 60-65 C-X-C motif chemokine ligand 8 Homo sapiens 205-218 7609578-8 1995 NaF (10 mM), which stimulates ACh release, produced parallel increases in EPPs and perineural Ca2+ currents. Acetylcholine 30-33 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 7875467-6 1995 Activation of PKC by phorbol myristate acetate also stimulated IL-8 production; however, the effects of IL-1 beta or TNF-alpha did not require PKC, as shown by the PKC inhibitor staurosporin or PKC depletion. Tetradecanoylphorbol Acetate 21-46 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7875467-8 1995 However, induction of IL-8 by IL-1 beta or TNF-alpha was reduced by the PTK inhibitors herbimycin (by 79% or 89%, respectively) and genistein (by > 95%). herbimycin 87-97 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 7875467-8 1995 However, induction of IL-8 by IL-1 beta or TNF-alpha was reduced by the PTK inhibitors herbimycin (by 79% or 89%, respectively) and genistein (by > 95%). Genistein 132-141 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 7751024-5 1995 More notably, the IL-4 treatment produced a pronounced elevation of mRNA for IL-3 and IL-8 when the cells were subsequently activated with ionomycin. Ionomycin 139-148 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 21556582-6 1995 Similar changes in IL-6 and IL-8 mRNA expression were noted when NUGC3 cells were cultured with paraformaldehyde-fixed 3T3 cells or the 3T3 membrane fraction, thereby supporting this notion. paraform 96-112 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 7531692-3 1995 Examination of the sequences of the CXC chemokines reveals that the highly conserved leucine, corresponding to Leu25 in IL-8, is always replaced by tyrosine in CC chemokines. Leucine 85-92 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 7864891-2 1995 Phorbol 12, 13 dibutyrate did not affect the IL-4-induced B cell growth; however, it reversed the IL-8-mediated inhibition, and this reversal was blocked by H7 (a protein kinase C inhibitor), but not by H8 (a protein kinase A inhibitor). Phorbol 12,13-Dibutyrate 0-25 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 7620820-0 1995 Inhibitory effect of FUT-175 on the production of interleukin 8 and polymorphonuclear leukocyte elastase. nafamostat 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 7531692-3 1995 Examination of the sequences of the CXC chemokines reveals that the highly conserved leucine, corresponding to Leu25 in IL-8, is always replaced by tyrosine in CC chemokines. Tyrosine 148-156 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 7531692-10 1995 Additionally, the Leu25-->Tyr mutation introduces a novel monocyte chemoattractant activity into IL-8. Tyrosine 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 7531692-11 1995 We therefore studied the displacement of [125I]MIP-1 alpha by IL-8 Leu25-->Tyr from the CC-CKR-1 receptor. Tyrosine 78-81 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 7531627-0 1995 IL-8/IL-8 receptor expression in psoriasis and the response to systemic tacrolimus (FK506) therapy. Tacrolimus 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7531627-0 1995 IL-8/IL-8 receptor expression in psoriasis and the response to systemic tacrolimus (FK506) therapy. Tacrolimus 72-82 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 7531627-0 1995 IL-8/IL-8 receptor expression in psoriasis and the response to systemic tacrolimus (FK506) therapy. Tacrolimus 84-89 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7531627-0 1995 IL-8/IL-8 receptor expression in psoriasis and the response to systemic tacrolimus (FK506) therapy. Tacrolimus 84-89 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 7531627-5 1995 IL-8 mRNA was not detected in the skin of any patient after the start of systemic tacrolimus therapy; IL-1 beta, IL-6 and IFN-gamma transcripts were also reduced. Tacrolimus 82-92 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7531627-8 1995 Estimation of circulating IL-8 levels by enzyme immunoassay showed that all patients with detectable IL-8 before treatment had decreased levels in response to treatment with tacrolimus; reductions in PASI scores were accompanied by decreases in IL-8 levels, that varied both in rate and extent. Tacrolimus 174-184 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 7531627-8 1995 Estimation of circulating IL-8 levels by enzyme immunoassay showed that all patients with detectable IL-8 before treatment had decreased levels in response to treatment with tacrolimus; reductions in PASI scores were accompanied by decreases in IL-8 levels, that varied both in rate and extent. Tacrolimus 174-184 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 7531627-8 1995 Estimation of circulating IL-8 levels by enzyme immunoassay showed that all patients with detectable IL-8 before treatment had decreased levels in response to treatment with tacrolimus; reductions in PASI scores were accompanied by decreases in IL-8 levels, that varied both in rate and extent. Tacrolimus 174-184 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 7531627-11 1995 They further suggest that interference with IL-8 production and/or that of other key chemokines may be an important mechanism underlying the therapeutic efficacy of tacrolimus, and other agents such as cyclosporin A, with similar molecular actions. Tacrolimus 165-175 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 7531627-11 1995 They further suggest that interference with IL-8 production and/or that of other key chemokines may be an important mechanism underlying the therapeutic efficacy of tacrolimus, and other agents such as cyclosporin A, with similar molecular actions. Cyclosporine 202-215 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 7531729-5 1995 When tested at 5 x 10(-9) mol/L, the decrease in histamine release by RANTES was 69.2% +/- 3.5%, by MIP-1 alpha 48.8% +/- 3.1%, by MIP-1 beta 42.9% +/- 3.1%, by PF4 56.5% +/- 2.9%, by IL-8 41.2% +/- 2.2, by CTAP III 27% +/- 4.4%, and by IP-10 15.3% +/- 2.6%. Histamine 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 184-188 7531729-10 1995 We have therefore characterized RANTES, MIP-1 alpha, MIP-1 beta, CTAP III, PF4, IL-8, and IP-10 as inhibitors of MCAF-induced histamine release. Histamine 126-135 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 7759774-0 1995 Enhancement of polymorphonuclear cell phagocytosis by lipid A-activated monocytes via cell-to-cell contact: a possible role for membrane-associated interleukin-6 and interleukin-8. Lipid A 54-61 C-X-C motif chemokine ligand 8 Homo sapiens 166-179 7822801-5 1995 Morphine but not opioid peptides interfered with activation and/or chemotaxis of the granulocytes induced by TNF-alpha, IL-1 alpha, IL-8, and FMLP (chemotactic peptide). Morphine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 7860742-7 1995 M. tuberculosis and its cell wall components lipoarabinomannan (LAM), lipomannan (LM), and phosphoinositolmannoside (PIM) stimulated IL-8 protein release and mRNA expression in vitro from alveolar macrophages, but deacylated LAM did not. lipoarabinomannan 45-62 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 7860742-7 1995 M. tuberculosis and its cell wall components lipoarabinomannan (LAM), lipomannan (LM), and phosphoinositolmannoside (PIM) stimulated IL-8 protein release and mRNA expression in vitro from alveolar macrophages, but deacylated LAM did not. lipoarabinomannan 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 7860742-7 1995 M. tuberculosis and its cell wall components lipoarabinomannan (LAM), lipomannan (LM), and phosphoinositolmannoside (PIM) stimulated IL-8 protein release and mRNA expression in vitro from alveolar macrophages, but deacylated LAM did not. lipomannan 70-80 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 7860742-7 1995 M. tuberculosis and its cell wall components lipoarabinomannan (LAM), lipomannan (LM), and phosphoinositolmannoside (PIM) stimulated IL-8 protein release and mRNA expression in vitro from alveolar macrophages, but deacylated LAM did not. lipomannan 82-84 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 7812007-4 1995 IL-8, NAP-2, and GRO alpha stimulated similar increases in the level of cytoplasmic free calcium. Calcium 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7860742-7 1995 M. tuberculosis and its cell wall components lipoarabinomannan (LAM), lipomannan (LM), and phosphoinositolmannoside (PIM) stimulated IL-8 protein release and mRNA expression in vitro from alveolar macrophages, but deacylated LAM did not. phosphatidylinositol mannoside 91-115 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 7860742-7 1995 M. tuberculosis and its cell wall components lipoarabinomannan (LAM), lipomannan (LM), and phosphoinositolmannoside (PIM) stimulated IL-8 protein release and mRNA expression in vitro from alveolar macrophages, but deacylated LAM did not. phosphatidylinositol mannoside 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 7829234-8 1995 In the absence of stimuli, TAM produced higher levels, compared to monocytes, of IL-6 and IL-8 but not of IL-1 and TNF. tam 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 7812007-6 1995 In contrast, only IL-8 enhanced the formation of phosphatidylethanol (PEt), the product catalyzed by phospholipase D (PLD) in the presence of ethanol. phosphatidylethanol 49-68 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 7812007-6 1995 In contrast, only IL-8 enhanced the formation of phosphatidylethanol (PEt), the product catalyzed by phospholipase D (PLD) in the presence of ethanol. Ethanol 61-68 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 7812007-7 1995 The formation of PEt stimulated by IL-8 was inhibited by pertussis toxin and the tyrosine kinase inhibitors erbstatin and herbimycin A. erbstatin 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 7851404-6 1995 The 72-residue interleukin-8 sequence starts with a serine residue, which can be oxidised under mild conditions to give a reactive glyoxylyl function which is then reacted with a nucleophilic fluorescein derivative. Serine 52-58 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 7851404-6 1995 The 72-residue interleukin-8 sequence starts with a serine residue, which can be oxidised under mild conditions to give a reactive glyoxylyl function which is then reacted with a nucleophilic fluorescein derivative. Fluorescein 192-203 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 7812007-7 1995 The formation of PEt stimulated by IL-8 was inhibited by pertussis toxin and the tyrosine kinase inhibitors erbstatin and herbimycin A. herbimycin 122-134 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 7812007-8 1995 The ability of IL-8 to stimulate the activity of PLD was additively enhanced, or primed, by cytochalasin B and by tumor necrosis factor alpha. Cytochalasin B 92-106 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 7618641-3 1995 HD using PMMA dialyzers also increased plasma IL-8 levels and induced slight expression of IL-8 mRNA. Polymethyl Methacrylate 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 7618641-3 1995 HD using PMMA dialyzers also increased plasma IL-8 levels and induced slight expression of IL-8 mRNA. Polymethyl Methacrylate 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 8624224-9 1995 The following can be concluded from this study: 1) silica based dentifrices containing MFP and NaF are effective at remineralizing caries-like lesions in both enamel and dentin; 2) there was no statistical difference between NaF and MFP in their ability to promote remineralization; and 3) pyrophosphate does not interfere with the remineralizing effects of NaF. Silicon Dioxide 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 7813101-3 1995 Spontaneous and lipopolysaccharide (LPS)-induced IL-8 release was significantly higher in PBM isolated from patients with IgA nephropathy (IgAN) and membranous nephropathy (MN) compared with normal controls. pbm 90-93 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 7558620-3 1995 Transcapillary diffusion of intravenously injected sodium fluorescein (NaF) was quantitated by videodensitometry in terms of fluorescent light intensities (FLIs) 5, 10, 20, 30, 60, 120, 180 and 300 s after the first appearance of the dye. Fluorescein 51-69 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 7559262-3 1995 Procaterol inhibited IL-8- and C5a-induced basophil migration in a dose-dependent fashion; 10(-7) M of procaterol reduced 30% of migration induced by both factors. Procaterol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 7559262-3 1995 Procaterol inhibited IL-8- and C5a-induced basophil migration in a dose-dependent fashion; 10(-7) M of procaterol reduced 30% of migration induced by both factors. Procaterol 103-113 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 8562581-2 1995 In the intact cell, NaF +/- aluminum was shown to activate various signal transduction pathways and indirect evidence is in line with effector mechanisms involving regulation of G-protein activity. Aluminum 28-36 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 8562581-4 1995 NaF was shown to reduce intracellular ATP levels and to suppress agonist-induced protein tyrosine phosphorylation and reactive oxygen species formation. Adenosine Triphosphate 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8562581-4 1995 NaF was shown to reduce intracellular ATP levels and to suppress agonist-induced protein tyrosine phosphorylation and reactive oxygen species formation. Tyrosine 89-97 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8562581-4 1995 NaF was shown to reduce intracellular ATP levels and to suppress agonist-induced protein tyrosine phosphorylation and reactive oxygen species formation. Reactive Oxygen Species 118-141 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8562581-5 1995 NaF led to in situ activation of nitrogen activated protein kinase, phospholipase A2 and PtdIns-phospholipase C. Addition of AlCl(3) or deferoxamine, a chelator of aluminum, had little or no effect on NaF mediated enzyme activation. Aluminum Chloride 125-132 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8562581-5 1995 NaF led to in situ activation of nitrogen activated protein kinase, phospholipase A2 and PtdIns-phospholipase C. Addition of AlCl(3) or deferoxamine, a chelator of aluminum, had little or no effect on NaF mediated enzyme activation. Deferoxamine 136-148 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8562581-5 1995 NaF led to in situ activation of nitrogen activated protein kinase, phospholipase A2 and PtdIns-phospholipase C. Addition of AlCl(3) or deferoxamine, a chelator of aluminum, had little or no effect on NaF mediated enzyme activation. Deferoxamine 136-148 C-X-C motif chemokine ligand 8 Homo sapiens 201-204 8562581-5 1995 NaF led to in situ activation of nitrogen activated protein kinase, phospholipase A2 and PtdIns-phospholipase C. Addition of AlCl(3) or deferoxamine, a chelator of aluminum, had little or no effect on NaF mediated enzyme activation. Aluminum 164-172 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8562581-6 1995 The results suggest that at least some of the pleiotropic effects of NaF in intact cells may not be mediated by G-protein activation but rather by depletion of ATP which is essential for protein phosphorylation reactions. Adenosine Triphosphate 160-163 C-X-C motif chemokine ligand 8 Homo sapiens 69-72 7837814-0 1995 Functional properties of HL60 cells matured with all-trans-retinoic acid and DMSO: differences in response to interleukin-8 and fMLP. Tretinoin 49-72 C-X-C motif chemokine ligand 8 Homo sapiens 110-123 7699821-4 1995 IL-8 increased significantly after the start of CPB and reached a peak at 10 minutes after release of the aortic cross-clamp, remaining significantly elevated until 10 minutes after the end of CPB (P < 0.05). cpb 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7837814-9 1995 Cells matured with DMSO responded to both IL-8 and fMLP in an equal manner with 1.6-fold increases in F-actin. Dimethyl Sulfoxide 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 7837814-10 1995 The 2 h migration for ATRA induced cells was 124 microns in response to IL-8, 107 microns with fMLP, and 105 microns in buffer. Tretinoin 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 7837814-11 1995 DMSO induced cells migrated 89 microns in response to IL-8, 106 microns with fMLP, and 66 microns in buffer. Dimethyl Sulfoxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 7837814-13 1995 In summary, HL60 cells cultured in ATRA develop greater functional maturity than those cultured in DMSO, and a greater responsiveness to IL-8 than fMLP, a finding distinct from previously reported work in neutrophils. Tretinoin 35-39 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 7699821-4 1995 IL-8 increased significantly after the start of CPB and reached a peak at 10 minutes after release of the aortic cross-clamp, remaining significantly elevated until 10 minutes after the end of CPB (P < 0.05). cpb 193-196 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7699821-7 1995 This study demonstrates elevated TNF alpha and IL-8 levels during CPB followed by increases of the neutrophil and the granulocyte elastase, which may be of importance in the systemic inflammatory response to CPB, especially in the development of postperfusion lung injury. cpb 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 22827272-6 1995 IL-8 production by TCC from the ocular fluid was further up-regulated upon stimulatation with PHA, but was suppressed by FK506 and hydrocortisone, though not by diclofenac sodium. Tacrolimus 121-126 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 7770008-1 1995 AlCl3, BeCl2 and NaF do not influence the insulin binding of Tetrahymena immediately after treatment, but 24 h later insulin binding is decreased or increased by NaF in a dose-dependent manner, AlCl3 barely influences the binding, and BeCl2 increases it. Aluminum Chloride 194-199 C-X-C motif chemokine ligand 8 Homo sapiens 162-165 7476567-1 1995 Previous findings provided evidence that bacterial lipopolysaccharide (LPS)-activated human monocytes are able to upregulate autologous polymorphonuclear (PMN) phagocytic ability via cell-to-cell contact mechanisms mediated by membrane (m)-associated cytokines (CKs), such as tumour necrosis factor (TNF)-alpha, interleukin (IL)-1 alpha, IL-1 beta, IL-6 and IL-8. bacterial lipopolysaccharide 41-69 C-X-C motif chemokine ligand 8 Homo sapiens 358-362 8587625-3 1995 A significant increase in GBM 35sulfate uptake was only seen when the glomeruli were cultured with the addition of IL-8 as compared with control cultures: 10.8 +/- (SEM) 1.7 and 7.9 +/- 1.4 cpm/micrograms GBM protein, respectively (p < 0.005). 35sulfate 30-39 C-X-C motif chemokine ligand 8 Homo sapiens 115-119 8587625-4 1995 IL-8 reproduces the effect of the reported supernatant factor on the GBM 35sulfate uptake. 35sulfate 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8587625-5 1995 Because IL-8 was detected in the supernatant of peripheral mononuclear cell cultures from idiopathic minimal-lesion nephrotic syndrome patients in relapse and because the increased GBM 35sulfate incorporation induced by the supernatant factor has been abolished by the addition to the culture media of anti-IL-8 neutralizing antibodies, we postulate that IL-8 is the previously described supernatant factor. 35sulfate 185-194 C-X-C motif chemokine ligand 8 Homo sapiens 8-12 22827272-6 1995 IL-8 production by TCC from the ocular fluid was further up-regulated upon stimulatation with PHA, but was suppressed by FK506 and hydrocortisone, though not by diclofenac sodium. Hydrocortisone 131-145 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 22827272-6 1995 IL-8 production by TCC from the ocular fluid was further up-regulated upon stimulatation with PHA, but was suppressed by FK506 and hydrocortisone, though not by diclofenac sodium. Diclofenac 161-178 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 22827272-7 1995 Colchicine rather increased IL-8 production by these TCC. Colchicine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 7571853-18 1995 EM and Roxythromycin, suppressed IL-8 production in Pseudomonas-stimulated neutrophils in a dose-dependent manner. Erythromycin 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 7571853-18 1995 EM and Roxythromycin, suppressed IL-8 production in Pseudomonas-stimulated neutrophils in a dose-dependent manner. roxythromycin 7-20 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 7571853-19 1995 1 alpha, 25-dihydroxy vitamin D3 also inhibited neutrophil-derived IL-8. Calcitriol 0-32 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 7502507-4 1995 Liberation of cytokines (IL-1, IL-6, IL-8) stimulates prostanoid synthesis in the decidua and amnion, as well as migration of granulocytes into the cervix. Prostaglandins 54-64 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 7828901-2 1994 The cDNA encodes a predicted sequence of 114 amino acids and contains the Cys motif C-X-C found in other members of the alpha-chemokine family which also includes interleukin 8 (IL-8). Cysteine 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 163-176 7806518-4 1994 While the basic fold is similar to that seen for interleukin-8 (IL-8) (Clore, G. M., Appella, E., Yamada, M., Matsushima, K., and Gronenborn, A. M. (1990) Biochemistry, 29, 1689-1696), there are differences in the ELR motif (residues 6-8), the turn involving residues 31-36, which is linked to the NH2-terminal region through the 9-35 disulfide bond. Disulfides 335-344 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 7828901-2 1994 The cDNA encodes a predicted sequence of 114 amino acids and contains the Cys motif C-X-C found in other members of the alpha-chemokine family which also includes interleukin 8 (IL-8). Cysteine 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 7821808-1 1994 The nucleotide (nt) sequence encoding the ovine homologue of interleukin-8 (IL-8) was determined. Nucleotides 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 7527448-5 1994 These IL-8R-B-specific mAbs were able to inhibit up to 90 and 50% of the 125I-labeled IL-8 binding to 293-27 cells and human neutrophils, respectively. Iodine-125 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 7821808-1 1994 The nucleotide (nt) sequence encoding the ovine homologue of interleukin-8 (IL-8) was determined. Nucleotides 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 7524649-6 1994 DHA also limited cytokine-stimulated endothelial cell expression of E-selectin and intercellular adhesion molecule 1 and the secretion of IL-6 and IL-8 into the medium but not the surface expression of constitutive surface molecules. Docosahexaenoic Acids 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 7949145-7 1994 Inhibition of PA formation, by the presence of ethanol, also inhibited the oxidative burst stimulation by IL-8. Phosphatidic Acids 14-16 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 7949145-7 1994 Inhibition of PA formation, by the presence of ethanol, also inhibited the oxidative burst stimulation by IL-8. Ethanol 47-54 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 7949145-9 1994 Collectively, these data show that IL-8 stimulates the metabolism of choline-containing phosphoglycerides in human PMN and support a role for PA in the signaling mechanisms used by IL-8 to stimulate PMN function. Choline 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 7949145-9 1994 Collectively, these data show that IL-8 stimulates the metabolism of choline-containing phosphoglycerides in human PMN and support a role for PA in the signaling mechanisms used by IL-8 to stimulate PMN function. Glycerophospholipids 88-105 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 7949145-9 1994 Collectively, these data show that IL-8 stimulates the metabolism of choline-containing phosphoglycerides in human PMN and support a role for PA in the signaling mechanisms used by IL-8 to stimulate PMN function. Phosphatidic Acids 142-144 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 7949145-9 1994 Collectively, these data show that IL-8 stimulates the metabolism of choline-containing phosphoglycerides in human PMN and support a role for PA in the signaling mechanisms used by IL-8 to stimulate PMN function. Phosphatidic Acids 142-144 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 7988196-16 1994 CONCLUSIONS: We conclude that asthmatics exposed to ozone develop a significant BALF neutrophilia and increased levels of the cytokines, IL-8 and IL-6. Ozone 52-57 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 7798535-7 1994 Treatment with inhaled beclomethasone dipropionate 500 micrograms twice a day led to a significant decrease in both the expression of GM-CSF (p < 0.01) and IL-8 (p < 0.02) and the number of EG2-staining cells (p < 0.01) in the epithelium. Beclomethasone 23-50 C-X-C motif chemokine ligand 8 Homo sapiens 159-163 7798535-10 1994 Also, beclomethasone dipropionate may inhibit eosinophil activation partly by downregulating the expression of GM-CSF and IL-8 in the bronchial epithelium. Beclomethasone 6-33 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 7875261-5 1994 We also determined the local effect of intratracheal administration of leumedin NPC 15669, an inhibitor of neutrophil recruitment, on IL-8- and Pseudomonas-induced neutrophil accumulation. Leumedin 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 7858873-14 1994 NaF (20 mM) and thrombin (EC50 0.4 u ml-1) also induced inositol phosphate formation in HUVEC. Inositol Phosphates 56-74 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 7525815-4 1994 On the other hand, an immunosuppressant, FK506, and a glucocorticoid inhibit the gene transcription as well as the production of IL-8. Tacrolimus 41-46 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 7525817-5 1994 For example, treatments of neutrophils with interleukin-8 (IL-8) or granulocyte colony-stimulating factor (G-CSF) potentiated the P-selectin-induced O2- production. Superoxides 149-151 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 7525817-5 1994 For example, treatments of neutrophils with interleukin-8 (IL-8) or granulocyte colony-stimulating factor (G-CSF) potentiated the P-selectin-induced O2- production. Superoxides 149-151 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 7754458-3 1994 Fluoride gel (1.1% NaF) was applied to the facial tooth surfaces of 10 elderly nursing home residents using a sponge-type intraoral applicator (IA). Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 7927762-5 1994 Preincubation of the cells with the protein tyrosine kinase inhibitors lavendustin A and tyrphostin 25 led to a reduction of the toxin-mediated effects on IL-8 release and IL-8 mRNA expression when Luk-PV and Alv were used as stimuli. lavendustin A 71-84 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 7927762-5 1994 Preincubation of the cells with the protein tyrosine kinase inhibitors lavendustin A and tyrphostin 25 led to a reduction of the toxin-mediated effects on IL-8 release and IL-8 mRNA expression when Luk-PV and Alv were used as stimuli. lavendustin A 71-84 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 7927762-5 1994 Preincubation of the cells with the protein tyrosine kinase inhibitors lavendustin A and tyrphostin 25 led to a reduction of the toxin-mediated effects on IL-8 release and IL-8 mRNA expression when Luk-PV and Alv were used as stimuli. Tyrphostins 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 7927762-5 1994 Preincubation of the cells with the protein tyrosine kinase inhibitors lavendustin A and tyrphostin 25 led to a reduction of the toxin-mediated effects on IL-8 release and IL-8 mRNA expression when Luk-PV and Alv were used as stimuli. Tyrphostins 89-99 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 7927772-5 1994 PMBC elicited large amounts of these cytokines, as well as IL-8 and TNF-beta, with an optimal release after 48 to 96 h. The most abundant cytokine produced in response to ETA was IL-8. pmbc 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 7927772-5 1994 PMBC elicited large amounts of these cytokines, as well as IL-8 and TNF-beta, with an optimal release after 48 to 96 h. The most abundant cytokine produced in response to ETA was IL-8. pmbc 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 7930619-4 1994 In this study, we demonstrate that adenosine inhibits the production of TNF-alpha, IL-6, and IL-8 by LPS-activated human monocytes with a differential potency. Adenosine 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 7930619-8 1994 In contrast, adenosine enhanced production of IL-6 and IL-8 by monocytes stimulated with IL-1 beta. Adenosine 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 7930619-9 1994 Furthermore, only 2-chloroadenosine, but not NECA, strongly inhibited cytokine-induced IL-6 and IL-8 production. 2-Chloroadenosine 18-35 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 7853122-9 1994 These results indicate that IL-8 production by HGF is synergistically stimulated by specific cytokines, IL-1 beta and TNF-alpha, and suggest that these stimulatory effects are down-regulated by IFN-gamma at the transcriptional level through PGE2-independent pathways. Dinoprostone 241-245 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 7943343-2 1994 TNF-alpha increased IL-8 mRNA and protein expression in HAEC in a concentration- and time-dependent manner and these effects were inhibited by dexamethasone (1 microM). Dexamethasone 143-156 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 7943343-5 1994 A549 cells also increased IL-8 secretion and mRNA after incubation of TNF-alpha, with inhibition by dexamethasone. Dexamethasone 100-113 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 7943343-4 1994 TNF-alpha-induced IL-8 mRNA expression showed a biphasic response in HAEC, with an early increase at 2 h followed by a sustained increase from 8 h, which was abolished by the addition of cycloheximide, suggesting that the synthesis of another protein was involved. Cycloheximide 187-200 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 7919340-0 1994 Histamine induces interleukin-8 secretion by endothelial cells. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 7919340-4 1994 The results showed that histamine increased the secretion and the mRNA expression of IL-8 by EC. Histamine 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 7919350-2 1994 Previous studies with the chemokine interleukin-8 (IL-8) had shown that the N-terminal region preceding the first cysteine residue was critical in defining neutrophil-activating properties. Cysteine 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 36-49 7919340-5 1994 Histamine-induced IL-8 production was (1) dose-dependent (at a dose > or = 10(-6) mol/L), (2) potentialized by costimulation with tumor necrosis factor (TNF)-alpha, (3) inhibited by H1 or H2 histamine receptor antagonists, and (4) significantly increased 4 hours after the initial stimulation. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 7919350-2 1994 Previous studies with the chemokine interleukin-8 (IL-8) had shown that the N-terminal region preceding the first cysteine residue was critical in defining neutrophil-activating properties. Cysteine 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 7919340-6 1994 These data suggest that histamine may be involved in the control of the late inflammatory reaction associated to allergic disorders through IL-8 secretion by EC. Histamine 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 7925583-0 1994 Staurosporine restores signaling and inhibits interleukin-8-induced chemotactic desensitization. Staurosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 7925583-5 1994 Using two-dimensional analysis we have shown that IL-8 induced a rapid serine/threonine phosphorylation of a number of neutrophil substrates the most prominent being phosphoprotein 39 (pp39), extracellular signal-related kinase-1, pp55 and pp66. Serine 71-77 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 7835945-0 1994 Pentoxifylline in vivo down-regulates the release of IL-1 beta, IL-6, IL-8 and tumour necrosis factor-alpha by human peripheral blood mononuclear cells. Pentoxifylline 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 7925583-5 1994 Using two-dimensional analysis we have shown that IL-8 induced a rapid serine/threonine phosphorylation of a number of neutrophil substrates the most prominent being phosphoprotein 39 (pp39), extracellular signal-related kinase-1, pp55 and pp66. Threonine 78-87 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 7925583-8 1994 When neutrophils were pretreated with staurosporine, prior to desensitization, phosphorylation of pp39 was observed upon restimulation with IL-8. Staurosporine 38-51 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 7925583-10 1994 Thus, homologous desensitization of neutrophils in response to IL-8 does not result from changes in receptor expression, but rather from a staurosporine-sensitive inactivation of subsequent signal transduction. Staurosporine 139-152 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7835984-4 1994 By analogy with the most prevalent form of hIL-8, a 72 amino acid form of oIL-8 was expressed as a fusion protein containing glutathione-S-transferase and purified by affinity chromatography on a glutathione-Sepharose column yielding 8 mg IL-8/L broth culture. Oils 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 7835984-4 1994 By analogy with the most prevalent form of hIL-8, a 72 amino acid form of oIL-8 was expressed as a fusion protein containing glutathione-S-transferase and purified by affinity chromatography on a glutathione-Sepharose column yielding 8 mg IL-8/L broth culture. Oils 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 7835945-3 1994 Due to the therapeutic implications, the present study addressed the in vivo effects of PTX on the release of TNF-alpha, IL-1 beta, IL-6 and IL-8 by human peripheral blood mononuclear cells (PBMC). Pentoxifylline 88-91 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 7835945-4 1994 When PBMC were obtained from healthy volunteers ingesting 5 x 400 mg PTX orally for 2 days, the ability of PBMC cultured for 24 hr to release TNF-alpha was significantly reduced, while secretion of IL-1 beta, IL-6 and IL-8 was not affected. Pentoxifylline 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 218-222 7835945-9 1994 However, when PBMC were incubated with PTX for 24 hr, PTX removed thereafter by medium change and cells further cultured, the production not only of TNF-alpha but also of IL-1 beta, IL-6 and IL-8 was reduced, demonstrating that PTX exerts diverse (inhibitory) effects on cytokine release by PBMC. Pentoxifylline 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 7835945-9 1994 However, when PBMC were incubated with PTX for 24 hr, PTX removed thereafter by medium change and cells further cultured, the production not only of TNF-alpha but also of IL-1 beta, IL-6 and IL-8 was reduced, demonstrating that PTX exerts diverse (inhibitory) effects on cytokine release by PBMC. Pentoxifylline 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 7835945-9 1994 However, when PBMC were incubated with PTX for 24 hr, PTX removed thereafter by medium change and cells further cultured, the production not only of TNF-alpha but also of IL-1 beta, IL-6 and IL-8 was reduced, demonstrating that PTX exerts diverse (inhibitory) effects on cytokine release by PBMC. Pentoxifylline 54-57 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 7853361-1 1994 A light addressable potentiometric sensor was used to measure acetylcholinesterase (AChE) activity in order to evaluate the protective effects of quaternary compounds and NaF against enzyme phosphorylation and aging by two organophosphates. Organophosphates 223-239 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 7927669-0 1994 Role of interleukin-8 (IL-8) and an inhibitory effect of erythromycin on IL-8 release in the airways of patients with chronic airway diseases. Erythromycin 57-69 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 7927669-5 1994 When anti-human IL-8 immunoglobulin G was used for neutralizing neutrophil chemotactic factor (NCF) activities in BAL fluids, the mean reduction rate of NCF activities in CAD+PA patients was significantly higher than that in CAD-PA patients. cad+pa 171-177 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 7927669-5 1994 When anti-human IL-8 immunoglobulin G was used for neutralizing neutrophil chemotactic factor (NCF) activities in BAL fluids, the mean reduction rate of NCF activities in CAD+PA patients was significantly higher than that in CAD-PA patients. cad-pa 225-231 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 7927669-7 1994 Treatment with erythromycin caused significant reductions of neutrophil numbers, IL-8/albumin ratios, and NE/albumin ratios in BAL fluids from these patients. Erythromycin 15-27 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 7927669-8 1994 To elucidate the mechanism of erythromycin therapy, we also examined whether erythromycin suppressed IL-8 production by human alveolar macrophages and neutrophils in vitro. Erythromycin 77-89 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 7927669-9 1994 We demonstrated a moderate inhibitory effect of erythromycin on IL-8 production in Pseudomonas-stimulated neutrophils but not in alveolar macrophages. Erythromycin 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 7853361-4 1994 Sodium fluoride (NaF), the most effective protectant against phosphorylation and aging, and the quaternary ammonium compounds reduced significantly AChE inhibition by DFP and paraoxon, to similar degrees. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 7927669-11 1994 The clinical efficacy of erythromycin therapy for CAD patients might be partly mediated through a reduced IL-8 production, diminishing neutrophil accumulation and NE release in the airways. Erythromycin 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 7962609-6 1994 H pylori induced IL-8 secretion was reduced by heat killing, sonication, freeze thawing or formalin fixation of the bacteria. Formaldehyde 91-99 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 7947352-5 1994 Specifically, RU486 (at concentrations of 1-100 nM) exerts pure antagonist actions by almost completely reversing the inhibitory effects of the glucocorticoid dexamethasone (Dex) on the release of monocyte/macrophages-derived lymphokines, such as IL-1, IL-6, IL-8 and tumor necrosis factor-alpha (TNF-alpha). Mifepristone 14-19 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 7930675-5 1994 As such, auranofin was also studied for its effect on IL-8 production. Auranofin 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 7930675-6 1994 Auranofin and staurosporine, inhibitors of protein kinase C, inhibited phorbol-myristate-acetate-stimulated IL-8 production. Auranofin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 7930675-6 1994 Auranofin and staurosporine, inhibitors of protein kinase C, inhibited phorbol-myristate-acetate-stimulated IL-8 production. Staurosporine 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 7930675-6 1994 Auranofin and staurosporine, inhibitors of protein kinase C, inhibited phorbol-myristate-acetate-stimulated IL-8 production. Tetradecanoylphorbol Acetate 71-96 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 8089496-0 1994 Asbestos stimulates IL-8 production from human lung epithelial cells. Asbestos 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 8089496-4 1994 That the membrane signaling events responsible for asbestos-induced IL-8 production are distinct from those responsible for IL-8 induction by cytokines was confirmed by using membrane-stabilizing agents and protein synthesis inhibitors. Asbestos 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 8089498-6 1994 In the presence of cytochalasin B, only fMLP and C5a caused the activation of phospholipase D in intact leukocytes and enhanced desensitization of IL-8 and C5a but not fMLP receptors. Cytochalasin B 19-33 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 7523800-0 1994 Modulation of IL-8, IL-1 beta, and G-CSF secretion by all-trans retinoic acid in acute promyelocytic leukemia. Tretinoin 64-77 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 7947352-5 1994 Specifically, RU486 (at concentrations of 1-100 nM) exerts pure antagonist actions by almost completely reversing the inhibitory effects of the glucocorticoid dexamethasone (Dex) on the release of monocyte/macrophages-derived lymphokines, such as IL-1, IL-6, IL-8 and tumor necrosis factor-alpha (TNF-alpha). Dexamethasone 159-172 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 7947352-5 1994 Specifically, RU486 (at concentrations of 1-100 nM) exerts pure antagonist actions by almost completely reversing the inhibitory effects of the glucocorticoid dexamethasone (Dex) on the release of monocyte/macrophages-derived lymphokines, such as IL-1, IL-6, IL-8 and tumor necrosis factor-alpha (TNF-alpha). Dexamethasone 174-177 C-X-C motif chemokine ligand 8 Homo sapiens 259-263 7947352-6 1994 Dex decreased in a dose-dependent manner the release of the above four lymphokines, with an ID50 of 0.9 +/- 0.1, 4.76 +/- 0.4, 9.8 +/- 1.8, and 1.16 +/- 0.2 nM for IL-1, IL-6, IL-8 and TNF-alpha, respectively. Dexamethasone 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 176-180 8077662-5 1994 Furthermore, cyclosporin A, but not rapamycin, blocked the synergistic induction of IL-8 expression achieved with anti-CD3 and anti-CD28 costimulation. Cyclosporine 13-26 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 8069926-4 1994 In this report, we show that the IFN-gamma-dependent inhibition of IL-8 release by PMN stimulated with lipopolysaccharide (LPS), tumor necrosis factor (TNF), and/or interleukin-1 beta (IL-1 beta), but not with Y-IgG, is a transient phenomenon. y-igg 210-215 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 8083528-9 1994 Monocytes or monocyte tumor cells produce MCP-1 and/or IL-8 in response to cytokines, virus, double stranded RNA, bacterial endotoxin, mitogen or phorbol ester. Phorbol Esters 146-159 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 7972371-3 1994 The association constant of NaF with AlPcSn in aqueous solution was measured as 500 +/- 20 M-1. alpcsn 37-43 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 8090031-2 1994 Monocytes express the esterase isoenzyme (termed "monocyte-specific esterase", MSE) that can be inhibited by NaF in the alpha-naphthyl acetate cytochemical staining. alpha-naphthyl acetate 120-142 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 7962965-5 1994 Etretinate was shown to have an effect on either IL-1 alpha or IL-8 secretion in unstimulated NHKs. Etretinate 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 7962965-6 1994 In HSC-1, a human squamous cell carcinoma cell line cultured in 20% FCS/DMEM, inhibited IL-1 alpha secretion and enhanced IL-8 secretion. dmem 72-76 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 7962965-8 1994 Stimulation of NHKs with PMA significantly enhanced IL-1 alpha and IL-8 secretion, and these effects were inhibited by etretinate. Etretinate 119-129 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 8074242-0 1994 Hyperoxia stimulates interleukin-8 release from alveolar macrophages and U937 cells: attenuation by dexamethasone. Dexamethasone 100-113 C-X-C motif chemokine ligand 8 Homo sapiens 21-34 8062926-4 1994 Sulfatides enhanced expression of tumor necrosis factor, interleukin-8, and interleukin-1 beta, but not interleukin-12/natural killer cell stimulating factor mRNAs. Sulfoglycosphingolipids 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 8074242-9 1994 Finally, dexamethasone at concentrations of 10 microM, 1 microM, and 100 nM markedly reduced hyperoxia-induced IL-8 release and mRNA synthesis by U937 cells. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 8074242-10 1994 We conclude that IL-8 may be important in the pathogenesis of pulmonary oxygen toxicity and that therapeutic concentrations of dexamethasone can suppress production of this cytokine. Oxygen 72-78 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 7989497-8 1994 The perivascular location of IL-8 throughout the stages of the human menstrual cycle is consistent with its proposed biological role as a modulator of endometrial function, especially synergism with prostaglandin E and the transmigration of leukocytes. Prostaglandins E 199-214 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 8034699-3 1994 We then analyzed these receptor mutants for their ability to mobilize intracellular calcium upon stimulation with 10 nM IL-8. Calcium 84-91 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 7972306-8 1994 Application of NaF (20 mM) for 4 min as a rinse significantly enhanced all of the sweet compounds by at least 23%, except for 10 mM sodium saccharin and 6.5 mM D-tryptophan, while all control compounds were suppressed. Saccharin 132-148 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 7972306-8 1994 Application of NaF (20 mM) for 4 min as a rinse significantly enhanced all of the sweet compounds by at least 23%, except for 10 mM sodium saccharin and 6.5 mM D-tryptophan, while all control compounds were suppressed. D-Tryptophan 160-172 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 8034626-6 1994 No effects of the Rap1A mutants on cell viability, proliferation, expression of cell-surface markers, or phorbol 12-myristate 13-acetate-stimulated interleukin-8 generation were detected. Tetradecanoylphorbol Acetate 105-136 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 7967357-5 1994 Elevated urinary IL-8 levels during the acute phase or exacerbations were found to be decreased during spontaneous or steroid pulse therapy-induced convalescence in all patients examined. Steroids 118-125 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 8034699-6 1994 Our study shows that, besides the extracellular domain cysteines which may be critical for the overall folding of the receptor, three residues, Arg-199, Arg-203, and Asp-265, are important for IL-8 binding and IL-8-mediated signal transduction. Arginine 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 8034699-6 1994 Our study shows that, besides the extracellular domain cysteines which may be critical for the overall folding of the receptor, three residues, Arg-199, Arg-203, and Asp-265, are important for IL-8 binding and IL-8-mediated signal transduction. Arginine 144-147 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 8034699-6 1994 Our study shows that, besides the extracellular domain cysteines which may be critical for the overall folding of the receptor, three residues, Arg-199, Arg-203, and Asp-265, are important for IL-8 binding and IL-8-mediated signal transduction. Arginine 153-156 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 8034699-6 1994 Our study shows that, besides the extracellular domain cysteines which may be critical for the overall folding of the receptor, three residues, Arg-199, Arg-203, and Asp-265, are important for IL-8 binding and IL-8-mediated signal transduction. Aspartic Acid 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 8034699-6 1994 Our study shows that, besides the extracellular domain cysteines which may be critical for the overall folding of the receptor, three residues, Arg-199, Arg-203, and Asp-265, are important for IL-8 binding and IL-8-mediated signal transduction. Aspartic Acid 166-169 C-X-C motif chemokine ligand 8 Homo sapiens 210-214 7976312-1 1994 Interleukin-8 induces chemotaxis of neutrophils, basophils and T-lymphocytes, releases intracellular enzymes from neutrophils and histamine from basophils, and regulates the adhesion of neutrophils. Histamine 130-139 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 7865076-5 1994 Significantly more fluoride was found in plaque from subjects who were using the NaF dentifrices than in plaque from subjects who were using Na2FPO3 dentifrices of the same F content. Fluorides 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 7519403-8 1994 Dexamethasone also inhibited the induction of IL-6 and IL-8 RNA by IL-1 and TNF. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 7519401-6 1994 Cheek cells exhibited a low endogenous rate of oxygen consumption, which was stimulated by glucose or succinate and inhibited by KCN or NaF. Oxygen 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 7519403-3 1994 Dexamethasone blocks the induction of IL-6 and IL-8 by IL-1 or TNF. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 7519403-4 1994 In these studies, we determined whether dexamethasone interferes with the upregulation of IL-6 and IL-8 by downregulating expression of the IL-1 or TNF receptor genes. Dexamethasone 40-53 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 8089604-24 1994 Thrombin, LPS, interleukin-8 and ET-1, known calcium agonists could increase intracellular calcium in fibroblasts, amnion and uterine myocytes. Calcium 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 8089604-24 1994 Thrombin, LPS, interleukin-8 and ET-1, known calcium agonists could increase intracellular calcium in fibroblasts, amnion and uterine myocytes. Calcium 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 7517209-6 1994 In addition, supernatants of purified B-CLL cells cultured in the presence of 12-O-tetradecanoylphorbol-13-acetate showed chemotactic activity towards neutrophils; this activity was neutralized in the presence of an anti-IL-8 antiserum. Tetradecanoylphorbol Acetate 78-114 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 7922784-0 1994 Dexamethasone regulates IL-1 beta and TNF-alpha-induced interleukin-8 production in human bone marrow stromal and osteoblast-like cells. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 7922784-1 1994 We have investigated both constitutive- and cytokine-induced secretion of interleukin-8 (IL-8) and its regulation by dexamethasone and 17 beta-estradiol in normal human bone marrow stromal (HBMS), osteoblast-like cells (hOB), and osteosarcoma MG-63 cells. Estradiol 135-152 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 7922784-6 1994 Dexamethasone (10(-7) M) significantly inhibited IL-1 beta plus TNF-alpha stimulated IL-8 production in HBMS, MG-63, and hOB cells. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 7818993-3 1994 AFC-ME, but not AFC, inhibited NaF- and PMA-stimulated superoxide release. afc-me 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 8003341-0 1994 Leukotriene B4 stimulates human polymorphonuclear leukocytes to synthesize and release interleukin-8 in vitro. Leukotriene B4 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 87-100 7818993-3 1994 AFC-ME, but not AFC, inhibited NaF- and PMA-stimulated superoxide release. N-acetyl-S-farnesylcysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 7818993-3 1994 AFC-ME, but not AFC, inhibited NaF- and PMA-stimulated superoxide release. Superoxides 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 7948754-0 1994 Measurement of cell migration stimulated by interleukin 8: use of ATP chemiluminescence. Adenosine Triphosphate 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 44-57 7525460-0 1994 Interleukin-8 and RANTES induce the adhesion of the human basophilic cell line KU-812 to human endothelial cell monolayers. ku-812 79-85 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8088360-3 1994 Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. Cyclosporine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 8088360-3 1994 Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. Cyclosporine 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 8088360-3 1994 Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. Calcitriol 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 8088360-3 1994 Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. Calcitriol 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 8088360-3 1994 Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. calcipotriene 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 8088360-3 1994 Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. calcipotriene 26-38 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 8088360-3 1994 Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. Anthralin 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 88-101 8088360-3 1994 Cyclosporine, calcitriol, calcipotriol or dithranol caused a dose-dependent decrease in interleukin-8 binding to cultured human keratinocytes, while interleukin-8 binding to granulocytes was not affected. Anthralin 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 149-162 8013067-6 1994 In addition, IL-8 stimulated smooth muscle cells to produce prostaglandin E2, which can inhibit IL-8-induced smooth muscle cell proliferation. Dinoprostone 60-76 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 8013067-6 1994 In addition, IL-8 stimulated smooth muscle cells to produce prostaglandin E2, which can inhibit IL-8-induced smooth muscle cell proliferation. Dinoprostone 60-76 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 8013067-7 1994 In the presence of indomethacin (5 mumol/L), IL-8 (1 nmol/L) stimulated an increase in human and rat aortic smooth muscle cell number during a 3-day period of incubation by 61 +/- 16% and 59 +/- 7% (n = 4), respectively. Indomethacin 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 8013067-9 1994 Moreover, IL-8 stimulated rat aortic smooth muscle cell migration by 20-fold over the control value, with an EC50 value of 0.83 nmol/L; this chemotactic activity of IL-8 was also potentiated by indomethacin. Indomethacin 194-206 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 8013067-9 1994 Moreover, IL-8 stimulated rat aortic smooth muscle cell migration by 20-fold over the control value, with an EC50 value of 0.83 nmol/L; this chemotactic activity of IL-8 was also potentiated by indomethacin. Indomethacin 194-206 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 8027219-2 1994 We study here the regulation of the PiP2 cascade by TSH, ATP, NaF, and bradykinin. Phosphatidylinositol 4,5-Diphosphate 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 8027219-4 1994 Activation of the PiP2 cascade by TSH (10 mU/mL), NaF, bradykinin, ionomycin, and 12-O-tetradecanoylphorbol-13-acetate stimulates iodide organification. Phosphatidylinositol 4,5-Diphosphate 18-22 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 7912755-10 1994 Culture supernatants from blasts cultured with or without TPA showed the production of large amounts of IL-8, IL-6, TNF-alpha, MIP-1 alpha, IL-10 and interferon gamma and modest amounts of IL-1 alpha, GM-CSF and stem cell factor. Tetradecanoylphorbol Acetate 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 8003341-2 1994 Here we examine whether PMN synthesize and release IL-8 in response to stimulation by leukotriene B4 (LTB4). Leukotriene B4 86-100 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 8003341-10 1994 Northern blot analysis of total RNA from PMN using a 30 mer oligonucleotide for IL-8 demonstrated increased mRNA expression in LTB4-stimulated PMN compared with untreated PMN. Oligonucleotides 60-75 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 8004813-4 1994 In contrast, IL-10 was weakly expressed when fibroblasts were stimulated with LPS, IL-1 alpha or tumour necrosis factor-alpha (TNF-alpha), but the expression was enhanced in the presence of cycloheximide combined with optimal concentrations of LPS, IL-1 alpha or TNF-alpha, IL-1 alpha was a more potent stimulator than LPS for GM-CSF, IL-6, IL-8 and IL-10 expression, but not for IL-1 alpha and IL-1 beta. Cycloheximide 190-203 C-X-C motif chemokine ligand 8 Homo sapiens 341-345 8200045-5 1994 When the MLR was performed in the presence of NMA (500 microM), the production of IL-8 increased twofold (P < 0.05) and ENA-78 increased fivefold (P < 0.05), while MCP-1 and MIP-1 alpha were not significantly altered. nma 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 8200045-6 1994 These findings suggest that NMA, an inhibitor of the L-arginine metabolic pathway, may regulate the production of specific C-X-C chemokines, IL-8 and ENA-78, during a MLR. nma 28-31 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 8200045-6 1994 These findings suggest that NMA, an inhibitor of the L-arginine metabolic pathway, may regulate the production of specific C-X-C chemokines, IL-8 and ENA-78, during a MLR. Arginine 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 8004813-6 1994 Dexamethasone suppressed both gene expression and protein production of GM-CSF, IL-6 and IL-8 when fibroblasts were exposed to IL-1 alpha. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 7960166-2 1994 The objective was to compare the effect of four dose levels of sodium monofluorophosphate (SMFP) and a single dose level of sodium fluoride (NaF) on DMFS, DMFT, and DFS Interproximal indices. Sodium Fluoride 124-139 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 7960166-5 1994 Results indicated that the 2000 ppm F NaF group had significantly smaller DMFS increment than the 2000 ppm F SMFP group p < 0.005. dmfs 74-78 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 7960166-6 1994 The 2000 ppm F NaF group demonstrated an 18 per cent (26 per cent for children > 10 years at baseline) reduction in DMFS over the 1500 ppm F SMFP group, the 2500 ppm F group a 15 per cent (19 per cent) reduction, and the 2000 ppm F SMFP a 5 per cent (9 per cent) reduction. dmfs 119-123 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 7514637-0 1994 Zymosan-induced IL-8 release from human neutrophils involves activation via the CD11b/CD18 receptor and endogenous platelet-activating factor as an autocrine modulator. Zymosan 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 8188340-6 1994 Furthermore, the addition of TNF, GM-CSF, or IL-8 to whole blood increased the capacity of a subpopulation of PMN to bind N-formyl peptides, a phenomenon that could account, at least in part, for the strong H2O2 production in response to FMLP after priming by the cytokines. n-formyl peptides 122-139 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 8188340-6 1994 Furthermore, the addition of TNF, GM-CSF, or IL-8 to whole blood increased the capacity of a subpopulation of PMN to bind N-formyl peptides, a phenomenon that could account, at least in part, for the strong H2O2 production in response to FMLP after priming by the cytokines. Hydrogen Peroxide 207-211 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 8188340-5 1994 TNF, GM-CSF, and IL-8 strongly primed a subpopulation of PMN to produce H2O2 in response to N-formyl-methionyl-leucyl-phenylalanine (FMLP), while IL-1 alpha, IL-1 beta, and IL-6 failed to do so. Hydrogen Peroxide 72-76 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 8188340-5 1994 TNF, GM-CSF, and IL-8 strongly primed a subpopulation of PMN to produce H2O2 in response to N-formyl-methionyl-leucyl-phenylalanine (FMLP), while IL-1 alpha, IL-1 beta, and IL-6 failed to do so. N-Formylmethionine Leucyl-Phenylalanine 133-137 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 7514637-1 1994 We have investigated mechanisms that regulate the generation of IL-8 by human neutrophils on contact with zymosan particles in vitro. Zymosan 106-113 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 8006454-5 1994 Sodium lauryl sulfate, phenol, and croton oil induced increases in IL-8 production at non-cytotoxic concentrations in semi-confluent human keratinocyte cultures. Sodium Dodecyl Sulfate 0-21 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 7514637-2 1994 Zymosan stimulated IL-8 production, which increased with increasing particle numbers and was abolished by the protein synthesis inhibitor cycloheximide. Zymosan 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 8006454-5 1994 Sodium lauryl sulfate, phenol, and croton oil induced increases in IL-8 production at non-cytotoxic concentrations in semi-confluent human keratinocyte cultures. Phenol 23-29 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 7514637-2 1994 Zymosan stimulated IL-8 production, which increased with increasing particle numbers and was abolished by the protein synthesis inhibitor cycloheximide. Cycloheximide 138-151 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 8006454-5 1994 Sodium lauryl sulfate, phenol, and croton oil induced increases in IL-8 production at non-cytotoxic concentrations in semi-confluent human keratinocyte cultures. Croton Oil 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 7514637-3 1994 IL-8 was detectable in culture supernatant at 8 h reaching a maximum at 24 h. In all further experiments IL-8 was measured at 24 h. mAbs to neutrophil CD18 (60.3 and 6.5E) caused a marked suppression of IL-8 generation, but only if added up to 2 h after zymosan stimulation. Zymosan 254-261 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8006454-9 1994 Studies using neutralizing antibodies to tumor necrosis factor alpha and IL-1 alpha demonstrated that IL-8 induction by croton oil and phenol occurred directly rather than through autocrine circuits. Croton Oil 120-130 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 8006454-9 1994 Studies using neutralizing antibodies to tumor necrosis factor alpha and IL-1 alpha demonstrated that IL-8 induction by croton oil and phenol occurred directly rather than through autocrine circuits. Phenol 135-141 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 7514637-4 1994 An anti-CD11b mAb (KIM 225) substantially inhibited zymosan-induced IL-8 release. Zymosan 52-59 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 7514637-6 1994 Two selective platelet-activating factor (PAF) receptor antagonists, WEB 2086 and UK 74505, produced a profound suppression of IL-8 generation, when added within 30 min to 1 h of zymosan stimulation. Zymosan 179-186 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 7514637-8 1994 FMLP, PAF, and a stable PAF agonist did not stimulate significant IL-8 production, however, a calcium ionophore (A23187) did induce IL-8 release and this was suppressed by UK 74505. Calcium 94-101 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 7514637-8 1994 FMLP, PAF, and a stable PAF agonist did not stimulate significant IL-8 production, however, a calcium ionophore (A23187) did induce IL-8 release and this was suppressed by UK 74505. Calcimycin 113-119 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 8195701-0 1994 Role of the mevalonate pathway of isoprenoid synthesis in IL-8 generation by activated monocytic cells. Mevalonic Acid 12-22 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 7514637-9 1994 We conclude that zymosan-induced IL-8 generation involves stimulation of the neutrophil via a CD11b/CD18 receptor resulting in beta 2-integrin mediated activation of signal transduction mechanisms that leads to cytokine synthesis. Zymosan 17-24 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 8195701-0 1994 Role of the mevalonate pathway of isoprenoid synthesis in IL-8 generation by activated monocytic cells. Terpenes 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 8195701-5 1994 Under these conditions interleukin-8 (IL-8) production was attenuated (by 50-90%) in response to lipopolysaccharide, granulocyte-macrophage colony-stimulating factor, and phorbol myristate acetate. Tetradecanoylphorbol Acetate 171-196 C-X-C motif chemokine ligand 8 Homo sapiens 23-36 8204599-0 1994 1H NMR studies of interleukin 8 analogs: characterization of the domains essential for function. Hydrogen 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 8195701-5 1994 Under these conditions interleukin-8 (IL-8) production was attenuated (by 50-90%) in response to lipopolysaccharide, granulocyte-macrophage colony-stimulating factor, and phorbol myristate acetate. Tetradecanoylphorbol Acetate 171-196 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8195701-6 1994 Coincubation of reductase inhibitor-treated cells with mevalonate prevented the attenuation of IL-8 production by reductase inhibitors. Mevalonic Acid 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 8195701-7 1994 The effects of isoprenoid depletion on cytokine production were selective: IL-1 beta generation was not inhibited but the production of IL-6 and IL-8 was concomitantly suppressed. Terpenes 15-25 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 8195701-9 1994 We conclude that isoprenoid generation through the mevalonate pathway is a requirement for IL-8 induction by activated monocytic cells in vitro. Terpenes 17-27 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 8195701-9 1994 We conclude that isoprenoid generation through the mevalonate pathway is a requirement for IL-8 induction by activated monocytic cells in vitro. Mevalonic Acid 51-61 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 8204599-1 1994 1H NMR studies were carried out on interleukin 8 (IL-8) analogs in order to probe the structural features that are essential for receptor binding and function. Hydrogen 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 8204599-1 1994 1H NMR studies were carried out on interleukin 8 (IL-8) analogs in order to probe the structural features that are essential for receptor binding and function. Hydrogen 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 8164648-8 1994 First, the N51/IL-8I hybrid in which the N51/KC sequence between cysteines 2 and 3 (or first disulfide bond) is replaced by the corresponding sequence in IL-8 shows IL-8-like properties, indicating that this region is important for specific receptor recognition. Disulfides 93-102 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 7922353-5 1994 RESULTS: Using affinity co-electrophoresis we found that interleukin-8 preferentially bound a subfraction of heparin that also showed increased affinity for melanoma growth stimulating activity (also known as MGSA, GRO or GRO alpha). Heparin 109-116 C-X-C motif chemokine ligand 8 Homo sapiens 57-70 7922353-8 1994 This observation led to predictions about the relative affinities of heparan sulfate for interleukin-8 and platelet factor 4, predictions that were confirmed by further binding assays. Heparitin Sulfate 69-84 C-X-C motif chemokine ligand 8 Homo sapiens 89-124 7513312-7 1994 GM-CSF and G-CSF pretreatment increased the fluoride (NaF)-induced chemiluminescence response by up to 10-fold; the serine/threonine phosphatase inhibitor okadaic acid inhibited GM-CSF- and G-CSF-induced priming. Fluorides 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 7513312-7 1994 GM-CSF and G-CSF pretreatment increased the fluoride (NaF)-induced chemiluminescence response by up to 10-fold; the serine/threonine phosphatase inhibitor okadaic acid inhibited GM-CSF- and G-CSF-induced priming. Okadaic Acid 155-167 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 7513312-8 1994 NaF-induced histamine release was enhanced up to 60 and 30% by GM-CSF and G-CSF priming, respectively. Histamine 12-21 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8164648-5 1994 Third, although the changes in intracellular Ca2+ of fura-2/AM-preloaded human neutrophils elicited by N51/KC and IL-8 are similar, pretreatment of the cells with N51/KC did not result in a loss of response to a subsequent treatment with IL-8; in contrast, treatment with IL-8 did result in the subsequent desensitization to N51/KC. Fura-2 53-59 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 8175759-2 1994 A glucocorticoid, dexamethasone, inhibited the production of a leukocyte chemotactic cytokine, interleukin 8 (IL-8), as well as mRNA expression by a glioblastoma cell line, T98G, stimulated with interleukin 1 (IL-1). Dexamethasone 18-31 C-X-C motif chemokine ligand 8 Homo sapiens 95-108 8175759-2 1994 A glucocorticoid, dexamethasone, inhibited the production of a leukocyte chemotactic cytokine, interleukin 8 (IL-8), as well as mRNA expression by a glioblastoma cell line, T98G, stimulated with interleukin 1 (IL-1). Dexamethasone 18-31 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 8175759-3 1994 Dexamethasone also inhibited IL-8 promoter-driven chloramphenicol acetyltransferase (CAT) activities induced by IL-1, suggesting that dexamethasone inhibited IL-8 production mainly at the transcriptional level. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 8175759-3 1994 Dexamethasone also inhibited IL-8 promoter-driven chloramphenicol acetyltransferase (CAT) activities induced by IL-1, suggesting that dexamethasone inhibited IL-8 production mainly at the transcriptional level. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 8175759-3 1994 Dexamethasone also inhibited IL-8 promoter-driven chloramphenicol acetyltransferase (CAT) activities induced by IL-1, suggesting that dexamethasone inhibited IL-8 production mainly at the transcriptional level. Dexamethasone 134-147 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 8175759-3 1994 Dexamethasone also inhibited IL-8 promoter-driven chloramphenicol acetyltransferase (CAT) activities induced by IL-1, suggesting that dexamethasone inhibited IL-8 production mainly at the transcriptional level. Dexamethasone 134-147 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 8175759-6 1994 Trimerized kappa B sequence in the IL-8 gene was enough for conferring the induction by IL-1 and inhibition by dexamethasone of CAT activity. Dexamethasone 111-124 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 8175759-8 1994 Collectively, dexamethasone interfered with the binding of the most essential transcription factor, NF-kappa B, to its cognate cis-element, thereby suppressing the transcription of IL-8 gene. Dexamethasone 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 181-185 8166094-2 1994 and a 0.05% sodium fluoride (NaF) rinse would significantly reduce decalcification when compared with manual toothbrushing only (control group) or manual toothbrushing and daily use of a NaF rinse (rinse group). Sodium Fluoride 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 8166094-2 1994 and a 0.05% sodium fluoride (NaF) rinse would significantly reduce decalcification when compared with manual toothbrushing only (control group) or manual toothbrushing and daily use of a NaF rinse (rinse group). Sodium Fluoride 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 187-190 8072242-9 1994 Finally, the effect of IL-8 on the 35sulfate turnover of the glomerular basement membrane (GBM) sulfated compounds was evaluated in vitro. 35sulfate 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 8072242-10 1994 A significant decrease in the percentage of residual 35sulfate incorporated in the GBM (41 +/- 5, mean +/- SEM) was observed in cultures treated with IL-8 as compared to those that were not treated with IL-8 (58 +/- 8, P < 0.01). 35sulfate 53-62 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 8164648-8 1994 First, the N51/IL-8I hybrid in which the N51/KC sequence between cysteines 2 and 3 (or first disulfide bond) is replaced by the corresponding sequence in IL-8 shows IL-8-like properties, indicating that this region is important for specific receptor recognition. Cysteine 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 8162169-1 1994 The cellular effects of sodium fluoride (NaF) on human bone cells in vitro have been variable and dependent on the culture system used. Sodium Fluoride 24-39 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 8091005-1 1994 To elucidate the relationship between active oxygen and interleukin 8 (IL-8) in patients with septic adult respiratory distress syndrome (ARDS), we determined the serum levels of alpha-tocopherol, which has an antioxidant action, and IL-8 in seven patients with this disease. Oxygen 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 56-69 8091005-1 1994 To elucidate the relationship between active oxygen and interleukin 8 (IL-8) in patients with septic adult respiratory distress syndrome (ARDS), we determined the serum levels of alpha-tocopherol, which has an antioxidant action, and IL-8 in seven patients with this disease. Oxygen 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 8091005-3 1994 A significant correlation was found between serum alpha-tocopherol level and IL-8 level (r = -0.758, p = 0.0473). alpha-Tocopherol 50-66 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 8091005-4 1994 These findings suggest that IL-8 activates neutrophils, which produce active oxygen. Oxygen 77-83 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 8011012-3 1994 The influence of cefodizime (CAS 69739-16-8), a new broad spectrum cephalosporin with immunostimulatory effects, and ceftriaxone on the production of GM-CSF and IL-8 in HBEC primary cultures was investigated. cefodizime 17-27 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 8162169-7 1994 In the presence of 1,25-dihydroxycholecalciferol (10(-9) mol/l), NaF enhanced alkaline phosphatase (p < 0.05, N = 8), procollagen type I propeptide (p < 0.05, N = 7) and osteocalcin (p < 0.05, N = 7) production by hMS(OB) cells but not by hOB cells. Calcitriol 19-48 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 8162169-7 1994 In the presence of 1,25-dihydroxycholecalciferol (10(-9) mol/l), NaF enhanced alkaline phosphatase (p < 0.05, N = 8), procollagen type I propeptide (p < 0.05, N = 7) and osteocalcin (p < 0.05, N = 7) production by hMS(OB) cells but not by hOB cells. propeptide 140-150 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 8163658-2 1994 Incubation of human endothelial cells (ECs) in hypoxia, PO2 approximately 14-18 Torr, led to time-dependent release of IL-8 antigen into the conditioned medium; this was accompanied by increased chemotactic activity for PMNs, blocked by antibody to IL-8. PO-2 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 8163658-2 1994 Incubation of human endothelial cells (ECs) in hypoxia, PO2 approximately 14-18 Torr, led to time-dependent release of IL-8 antigen into the conditioned medium; this was accompanied by increased chemotactic activity for PMNs, blocked by antibody to IL-8. PO-2 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 249-253 8144938-4 1994 The protein synthesis inhibitor, cycloheximide, had no detectable effect on levels of IL-8 mRNA expression in PMN incubated in medium alone; however, cycloheximide could selectively modulate IL-8 mRNA transcription in PMN, depending on the cytokine used. Cycloheximide 33-46 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 8144938-4 1994 The protein synthesis inhibitor, cycloheximide, had no detectable effect on levels of IL-8 mRNA expression in PMN incubated in medium alone; however, cycloheximide could selectively modulate IL-8 mRNA transcription in PMN, depending on the cytokine used. Cycloheximide 150-163 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 8144935-6 1994 The t1/2 of MIP-1 alpha, MIP-1 beta, and IL-8 mRNA from PMNs treated for 4 h with LPS before actinomycin-D (Ac-D) addition were approximately 40 min, 1.7 h, and 2 h, respectively, whereas the t1/2 from PMNs stimulated for 8 h before Ac-D were 2, 2, and > 9 h, respectively. Dactinomycin 108-112 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 8144935-6 1994 The t1/2 of MIP-1 alpha, MIP-1 beta, and IL-8 mRNA from PMNs treated for 4 h with LPS before actinomycin-D (Ac-D) addition were approximately 40 min, 1.7 h, and 2 h, respectively, whereas the t1/2 from PMNs stimulated for 8 h before Ac-D were 2, 2, and > 9 h, respectively. Actinium 108-110 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 8144938-5 1994 Cycloheximide did not affect or alter IL-8 mRNA induction in IL-2-treated PMN but abrogated it in granulocyte macrophage-CSF-treated PMN and super-induced the level of IL-8 mRNA in C. albicans-treated PMN. Cycloheximide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 8144935-6 1994 The t1/2 of MIP-1 alpha, MIP-1 beta, and IL-8 mRNA from PMNs treated for 4 h with LPS before actinomycin-D (Ac-D) addition were approximately 40 min, 1.7 h, and 2 h, respectively, whereas the t1/2 from PMNs stimulated for 8 h before Ac-D were 2, 2, and > 9 h, respectively. Deuterium 105-106 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 8140420-2 1994 An IL-8 analog was chemically synthesized, with the amide nitrogen of leucine-25 methylated to selectivity block formation of hydrogen bonds between monomers and thereby prevent dimerization. Amides 52-57 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 8140420-2 1994 An IL-8 analog was chemically synthesized, with the amide nitrogen of leucine-25 methylated to selectivity block formation of hydrogen bonds between monomers and thereby prevent dimerization. Nitrogen 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 8140420-2 1994 An IL-8 analog was chemically synthesized, with the amide nitrogen of leucine-25 methylated to selectivity block formation of hydrogen bonds between monomers and thereby prevent dimerization. Leucine 70-77 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 8140420-2 1994 An IL-8 analog was chemically synthesized, with the amide nitrogen of leucine-25 methylated to selectivity block formation of hydrogen bonds between monomers and thereby prevent dimerization. Hydrogen 126-134 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 8120414-0 1994 Actin polymerization, calcium-transients, and phospholipid metabolism in human neutrophils after stimulation with interleukin-8 and N-formyl peptide. Phospholipids 46-58 C-X-C motif chemokine ligand 8 Homo sapiens 114-127 7510691-0 1994 The interleukin-8 AP-1 and kappa B-like sites are genetic end targets of FK506-sensitive pathway accompanied by calcium mobilization. Tacrolimus 73-78 C-X-C motif chemokine ligand 8 Homo sapiens 4-17 7510691-0 1994 The interleukin-8 AP-1 and kappa B-like sites are genetic end targets of FK506-sensitive pathway accompanied by calcium mobilization. Calcium 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 4-17 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Tacrolimus 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Tacrolimus 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Tetradecanoylphorbol Acetate 151-182 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Tetradecanoylphorbol Acetate 151-182 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Tetradecanoylphorbol Acetate 184-187 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Tetradecanoylphorbol Acetate 184-187 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Calcium 193-200 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Calcium 193-200 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Ionomycin 219-228 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 7510691-2 1994 We observed that FK506 suppressed the transcription of a chemotactic cytokine, interleukin-8 (IL-8) in a human T cell line, Jurkat cells, activated by phorbol 12-myristate 13-acetate (PMA) and calcium (Ca2+) ionophore (ionomycin). Ionomycin 219-228 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 7510691-3 1994 By deleted and mutated analysis of the IL-8 promoters, the AP-1 and kappa B-like sites were identified as the responsive elements for PMA and ionomycin. Ionomycin 142-151 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 7510691-7 1994 Furthermore, we confirmed the previous report that FK506 suppressed the PMA/ionomycin-induced activation through authentic kappa B site of immunoglobulin (Ig) gene, to which NF-kappa B binding was also decreased by FK506, indicating that both IL-8 kappa B-like site and Ig kappa B site are FK506-sensitive in spite of the difference of binding factors. Tacrolimus 51-56 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 7510691-7 1994 Furthermore, we confirmed the previous report that FK506 suppressed the PMA/ionomycin-induced activation through authentic kappa B site of immunoglobulin (Ig) gene, to which NF-kappa B binding was also decreased by FK506, indicating that both IL-8 kappa B-like site and Ig kappa B site are FK506-sensitive in spite of the difference of binding factors. Ionomycin 76-85 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 7510691-7 1994 Furthermore, we confirmed the previous report that FK506 suppressed the PMA/ionomycin-induced activation through authentic kappa B site of immunoglobulin (Ig) gene, to which NF-kappa B binding was also decreased by FK506, indicating that both IL-8 kappa B-like site and Ig kappa B site are FK506-sensitive in spite of the difference of binding factors. Tacrolimus 215-220 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 7510691-7 1994 Furthermore, we confirmed the previous report that FK506 suppressed the PMA/ionomycin-induced activation through authentic kappa B site of immunoglobulin (Ig) gene, to which NF-kappa B binding was also decreased by FK506, indicating that both IL-8 kappa B-like site and Ig kappa B site are FK506-sensitive in spite of the difference of binding factors. Tacrolimus 215-220 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 7510691-8 1994 Our results indicate that not only the reported IL-2 NF-AT and NFIL-2A sites and Ig kappa B site, but also the IL-8 AP-1 and kappa B-like sites are terminals of FK506-sensitive pathway involving Ca2+ mobilization. Tacrolimus 161-166 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 8198453-0 1994 [Fluticasone propionate reduced the production of GM-CSF, IL-6 and IL-8 generated from cultured nasal epithelial cells]. Fluticasone 1-23 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 8118041-9 1994 Both intracellular H2O2 and phagocytosis assays from group III but not groups I-II showed exaggerated upregulation when exposed to NaF (4 mmol/L). Hydrogen Peroxide 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 8206512-0 1994 Inhibition of interleukin-8 expression by dexamethasone in human cultured airway epithelial cells. Dexamethasone 42-55 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 8206512-3 1994 We have investigated the effect of dexamethasone on IL-8 expression in primary cultured HAEC obtained from transplantation donors. Dexamethasone 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 8206512-6 1994 Dexamethasone suppressed IL-8 mRNA expression and protein synthesis dose-dependently in both resting and stimulated HAEC. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 8206512-7 1994 The half-life of IL-8 mRNA determined in the presence of actinomycin D was less than 1 hr, and dexamethasone preincubation had no effect on mRNA stability. Dactinomycin 57-70 C-X-C motif chemokine ligand 8 Homo sapiens 17-21 9522744-0 1994 Fluoride profiles of enamel following topical application of neutral and acidulated NaF solution using x-ray photoelectron spectroscopy (ESCA)--an in vitro study. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 84-87 8142378-7 1994 When the incubation medium was supplemented with NaF and AlCl3, and maintained in the dark, both 2-azido[3H]ADP and 8-azido[3H]ADP were able to elicit inhibition of F1-ATPase activity, exactly like ADP did. 2-azido[3h]adp 97-111 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 8142378-7 1994 When the incubation medium was supplemented with NaF and AlCl3, and maintained in the dark, both 2-azido[3H]ADP and 8-azido[3H]ADP were able to elicit inhibition of F1-ATPase activity, exactly like ADP did. 8-azido[3h]adp 116-130 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 8142378-7 1994 When the incubation medium was supplemented with NaF and AlCl3, and maintained in the dark, both 2-azido[3H]ADP and 8-azido[3H]ADP were able to elicit inhibition of F1-ATPase activity, exactly like ADP did. Adenosine Diphosphate 108-111 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 8117443-0 1994 Interleukin-1-mediated release of interleukin-8 by asbestos-stimulated human pleural mesothelial cells. Asbestos 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 8117443-4 1994 Suspensions of amosite, chrysotile, or crocidolite asbestos in concentrations as low as 5 micrograms/ml enhanced release of IL-8 from HPMC during 6 h of incubation at 37 degrees C. Electron microscopy of asbestos-treated HPMC showed that the cells avidly engulfed each of the different types of asbestos fibers. Asbestos, Amosite 15-22 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8117443-4 1994 Suspensions of amosite, chrysotile, or crocidolite asbestos in concentrations as low as 5 micrograms/ml enhanced release of IL-8 from HPMC during 6 h of incubation at 37 degrees C. Electron microscopy of asbestos-treated HPMC showed that the cells avidly engulfed each of the different types of asbestos fibers. Asbestos, Crocidolite 39-59 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8117443-4 1994 Suspensions of amosite, chrysotile, or crocidolite asbestos in concentrations as low as 5 micrograms/ml enhanced release of IL-8 from HPMC during 6 h of incubation at 37 degrees C. Electron microscopy of asbestos-treated HPMC showed that the cells avidly engulfed each of the different types of asbestos fibers. Asbestos 51-59 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8117443-4 1994 Suspensions of amosite, chrysotile, or crocidolite asbestos in concentrations as low as 5 micrograms/ml enhanced release of IL-8 from HPMC during 6 h of incubation at 37 degrees C. Electron microscopy of asbestos-treated HPMC showed that the cells avidly engulfed each of the different types of asbestos fibers. hydroxypropylmethylcellulose-lactose matrix 134-138 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 8117443-6 1994 Identity of IL-8 in HPMC supernatants was established by absorption with an antibody to IL-8. hydroxypropylmethylcellulose-lactose matrix 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 12-16 8117443-6 1994 Identity of IL-8 in HPMC supernatants was established by absorption with an antibody to IL-8. hydroxypropylmethylcellulose-lactose matrix 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 8117443-7 1994 Preincubation of HPMC with IL-1 receptor antagonist (IL-1ra) significantly decreased release of IL-8 after stimulation with amosite or crocidolite asbestos. hydroxypropylmethylcellulose-lactose matrix 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 8117443-7 1994 Preincubation of HPMC with IL-1 receptor antagonist (IL-1ra) significantly decreased release of IL-8 after stimulation with amosite or crocidolite asbestos. Asbestos, Amosite 124-131 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 8117443-7 1994 Preincubation of HPMC with IL-1 receptor antagonist (IL-1ra) significantly decreased release of IL-8 after stimulation with amosite or crocidolite asbestos. Asbestos, Crocidolite 135-155 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 8117443-8 1994 We conclude that HPMC release IL-8 in response to asbestos stimulation and that the response is, in part, mediated by IL-1, mainly in the form of IL-1 alpha. hydroxypropylmethylcellulose-lactose matrix 17-21 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 8117443-8 1994 We conclude that HPMC release IL-8 in response to asbestos stimulation and that the response is, in part, mediated by IL-1, mainly in the form of IL-1 alpha. Asbestos 50-58 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 8031999-8 1994 Of three disease-modifying drugs tested, dexamethasone and gold sodium thiomalate (GST) inhibited the production of IL-8 and MCP-1, while methotrexate (MTX) was inactive. Dexamethasone 41-54 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 8031999-8 1994 Of three disease-modifying drugs tested, dexamethasone and gold sodium thiomalate (GST) inhibited the production of IL-8 and MCP-1, while methotrexate (MTX) was inactive. sodium thiomalate 64-81 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 8031999-8 1994 Of three disease-modifying drugs tested, dexamethasone and gold sodium thiomalate (GST) inhibited the production of IL-8 and MCP-1, while methotrexate (MTX) was inactive. Gold Sodium Thiomalate 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 8031999-9 1994 Dexamethasone reduced the production of MCP-1 and IL-8 by 20-65% and 60-80%, respectively, whilst GST inhibited MCP-1 and IL-8 synthesis in suboptimally, but not in optimally stimulated synoviocytes. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 8133058-6 1994 We observed complete cross-competition of unlabeled IL-8 with 125I-labeled-NAP-2 and of unlabeled NAP-2 with 125I-labeled IL-8, indicating the absence of monospecific binding sites for either chemokine. Iodine-125 109-113 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 8120414-2 1994 Stimulation of human neutrophils with IL-8 induced a rapid polymerization of actin as detected by 7-nitrobenz-2-oxa-1,3-diazol-(NBD)-phallacidin staining of f-actin and reduction of monitored right-angle light scatter. 7-nitrobenz-2-oxa-1,3-diazol-(nbd) 98-132 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8120414-2 1994 Stimulation of human neutrophils with IL-8 induced a rapid polymerization of actin as detected by 7-nitrobenz-2-oxa-1,3-diazol-(NBD)-phallacidin staining of f-actin and reduction of monitored right-angle light scatter. phallacidin 133-144 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8120414-6 1994 Moreover, [32P]phosphatidic acid (PA) production stimulated by IL-8 was minimal and transient as compared to the response activated by N-formyl peptide. [32p]phosphatidic acid 10-32 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 8120414-6 1994 Moreover, [32P]phosphatidic acid (PA) production stimulated by IL-8 was minimal and transient as compared to the response activated by N-formyl peptide. Protactinium 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 8120414-9 1994 This study indicates that IL-8 is a potent activator of intracellular events presumably required for chemotaxis, but a relatively weak activator for events associated with superoxide anion generation and proinflammatory activity. Superoxides 172-188 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 7735949-8 1994 Therefore, ET-1-treated monocytes probably upregulate neutrophil superoxide production via a mechanism which includes IL-8. Superoxides 65-75 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 8032126-2 1994 Sodium fluoride (NaF) did not affect the extracellular pH of sperm, except that a slight acidification was caused by the 250 mM dose only. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 8032126-6 1994 Sperm glutathione levels also showed a time-dependent decrease with complete depletion after 20 min indicating rapid glutathione oxidation in detoxification of the NaF. Glutathione 6-17 C-X-C motif chemokine ligand 8 Homo sapiens 164-167 8032126-6 1994 Sperm glutathione levels also showed a time-dependent decrease with complete depletion after 20 min indicating rapid glutathione oxidation in detoxification of the NaF. Glutathione 117-128 C-X-C motif chemokine ligand 8 Homo sapiens 164-167 8145725-5 1994 Halothane (1%) increased basal as well as isoprenaline-, NaF-, cholera toxin-, and guanylylimidodiphosphate [Gpp(NH)p]-stimulated adenylate cyclase in human myocardial membranes (p < 0.05). Halothane 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 7907421-4 1994 A ligand for p185, neu-activating factor (NAF), specifically binds to neu receptor and increases the p185c-neu tyrosine phosphorylation in vitro and in vivo in a dose-dependent manner. Tyrosine 111-119 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 7508438-0 1994 Sulfatides trigger increase of cytosolic free calcium and enhanced expression of tumor necrosis factor-alpha and interleukin-8 mRNA in human neutrophils. Sulfoglycosphingolipids 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 7515597-5 1994 This method was applied to cloning of a cDNA encoding interleukin 8 (IL-8) from a cDNA library prepared from phorbol myristate acetate-treated U937 cells. Tetradecanoylphorbol Acetate 109-134 C-X-C motif chemokine ligand 8 Homo sapiens 54-67 7515597-5 1994 This method was applied to cloning of a cDNA encoding interleukin 8 (IL-8) from a cDNA library prepared from phorbol myristate acetate-treated U937 cells. Tetradecanoylphorbol Acetate 109-134 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 7908651-1 1994 Porphyromonas gingivalis fimbriae as well as synthetic peptides that mimic the fimbrial subunit protein, which includes the amino acid sequence XLTXXLTXXNXX, induced high production of proinflammatory cytokines such as interleukin-1 beta, interleukin-6, interleukin-8, tumor necrosis factor-alpha in human peripheral blood monocyte/macrophage cultures. Peptides 55-63 C-X-C motif chemokine ligand 8 Homo sapiens 254-296 7508438-9 1994 Sulfatides also triggered an increase of tumor necrosis factor-alpha and interleukin-8 mRNAs in neutrophils. Sulfoglycosphingolipids 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 8027281-4 1994 In endometrium, the stage of the menstrual cycle did not affect IL-8 production but a 10(-6) M concentration of progesterone or dexamethasone significantly reduced the concentration of IL-8 in medium after 24 h. After a further 24 h with lipopolysaccharide (LPS) stimulation, only MPA and dexamethasone inhibited production significantly. Progesterone 112-124 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 8027281-6 1994 The IL-8 produced in uterine tissues might act synergistically with prostaglandin E (PGE), a likely site for this interaction being blood vessels where PGE production is also repressed by progesterone. Prostaglandins E 68-83 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 8027281-4 1994 In endometrium, the stage of the menstrual cycle did not affect IL-8 production but a 10(-6) M concentration of progesterone or dexamethasone significantly reduced the concentration of IL-8 in medium after 24 h. After a further 24 h with lipopolysaccharide (LPS) stimulation, only MPA and dexamethasone inhibited production significantly. Dexamethasone 128-141 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 8027281-6 1994 The IL-8 produced in uterine tissues might act synergistically with prostaglandin E (PGE), a likely site for this interaction being blood vessels where PGE production is also repressed by progesterone. Prostaglandins E 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 8027281-6 1994 The IL-8 produced in uterine tissues might act synergistically with prostaglandin E (PGE), a likely site for this interaction being blood vessels where PGE production is also repressed by progesterone. Prostaglandins E 152-155 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 8027281-4 1994 In endometrium, the stage of the menstrual cycle did not affect IL-8 production but a 10(-6) M concentration of progesterone or dexamethasone significantly reduced the concentration of IL-8 in medium after 24 h. After a further 24 h with lipopolysaccharide (LPS) stimulation, only MPA and dexamethasone inhibited production significantly. Dexamethasone 289-302 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 8027281-6 1994 The IL-8 produced in uterine tissues might act synergistically with prostaglandin E (PGE), a likely site for this interaction being blood vessels where PGE production is also repressed by progesterone. Progesterone 188-200 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 8027281-5 1994 In chorion cells, IL-8 production was significantly decreased by both MPA and dexamethasone in the LPS stimulated cells but the reduction in the first 24 h was not significant. Dexamethasone 78-91 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 8113959-0 1994 Liposomal muramyl tripeptide up-regulates interleukin-1 alpha, interleukin-1 beta, tumor necrosis factor-alpha, interleukin-6 and interleukin-8 gene expression in human monocytes. muramyl tripeptide 10-28 C-X-C motif chemokine ligand 8 Homo sapiens 130-143 8193081-0 1994 Regulatory effects of 1,25-dihydroxyvitamin D3 and a novel vitamin D3 analogue MC903 on secretion of interleukin-1 alpha (IL-1 alpha) and IL-8 by normal human keratinocytes and a human squamous cell carcinoma cell line (HSC-1). Cholecalciferol 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 8193081-5 1994 In the present study, we investigated the effects of 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) and its analogue MC903 on IL-1 alpha and IL-8 secretion by human keratinocytes in vitro. Calcitriol 53-79 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 8193081-5 1994 In the present study, we investigated the effects of 1,25-dihydroxyvitamin D3 (1,25(OH)2D3) and its analogue MC903 on IL-1 alpha and IL-8 secretion by human keratinocytes in vitro. Calcitriol 79-90 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 8193081-10 1994 Stimulation of NHKs with phorbol 12-myristate 13-acetate(PMA) and lipopolysaccharide(LPS) resulted in an increase of IL-8 and decrease of IL-1 alpha in the culture supernatants. Tetradecanoylphorbol Acetate 25-56 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 8193081-10 1994 Stimulation of NHKs with phorbol 12-myristate 13-acetate(PMA) and lipopolysaccharide(LPS) resulted in an increase of IL-8 and decrease of IL-1 alpha in the culture supernatants. Tetradecanoylphorbol Acetate 57-60 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 8193081-11 1994 Addition of 1,25(OH)2D3 or MC903 inhibited the increased secretion of IL-8 but restored decreased secretion of IL-1 alpha from stimulated NHKs dose dependently. Calcitriol 12-23 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 8193081-11 1994 Addition of 1,25(OH)2D3 or MC903 inhibited the increased secretion of IL-8 but restored decreased secretion of IL-1 alpha from stimulated NHKs dose dependently. calcipotriene 27-32 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 8193081-12 1994 Hydrocortisone and cyclosporin A showed similar inhibitory effects on PMA/LPS-increased IL-8 secretion from NHKs but had little effect of restoring IL-1 alpha. Hydrocortisone 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 8193081-12 1994 Hydrocortisone and cyclosporin A showed similar inhibitory effects on PMA/LPS-increased IL-8 secretion from NHKs but had little effect of restoring IL-1 alpha. Cyclosporine 19-32 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 8193081-12 1994 Hydrocortisone and cyclosporin A showed similar inhibitory effects on PMA/LPS-increased IL-8 secretion from NHKs but had little effect of restoring IL-1 alpha. Tetradecanoylphorbol Acetate 70-73 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 8113959-4 1994 Monocyte interleukin (IL)-1 alpha, IL-1 beta, IL-6, IL-8 and tumor necrosis factor (TNF)-alpha expression were all up-regulated after a 2-h incubation with L-MTP-PE. L-MTP-PE 156-164 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 8307164-3 1994 A peptide corresponding to residues 1-40 of the IL-8 type 1 receptor (IL8-r1) was titrated into a sample of uniformly 15N-labeled IL-8. 15n 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 8202627-0 1994 Inhibition of IL-6 and IL-8 production in human fibroblast cell lines by 1,25 (OH)2 vitamin D3 and two of its analogs with lower calcemic activity. Calcitriol 73-94 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 8202627-1 1994 In human fibroblast cultures TPA increased IL-6 and IL-8 production. Tetradecanoylphorbol Acetate 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 8307164-3 1994 A peptide corresponding to residues 1-40 of the IL-8 type 1 receptor (IL8-r1) was titrated into a sample of uniformly 15N-labeled IL-8. 15n 118-121 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 8001052-5 1994 Data from these studies established the ability of the in vitro model to provide reproducible results, to demonstrate significant dose-related differences in the effects of both NaF- and Na2PO3F-containing treatments on dentin fluoride uptake and demineralization, and to detect a fluoride-induced reduction in dentin caries, relative to a nonfluoride control, similar to results established in a clinical trial. Fluorides 227-235 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 8276881-14 1994 The ability of LPS to induce IL-8 expression was suppressed by recombinant human IL-4 and dexamethasone in a concentration-dependent manner. Dexamethasone 90-103 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 8073837-7 1994 IL-8 and huGRO mRNAs were constitutively produced in KC, as was demonstrated after incubation with cycloheximide. Cycloheximide 99-112 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8187790-0 1993 Inhibition of endotoxin-induced interleukin 8 release by teicoplanin in human whole blood. Teicoplanin 57-68 C-X-C motif chemokine ligand 8 Homo sapiens 32-45 8281849-6 1994 At the cellular level, 5-aminosalicylic acid inhibited phorbol myristate acetate (100 ng/ml)-activated superoxide generation to 82.3 +/- 9.3%, the formylmethionyl leucyl peptide (10(-5) M) to 61.0 +/- 6.8%, and the NaF (20 mM)-stimulated production to 32.3 +/- 3.2% (mean +/- SD, P < 0.01). Mesalamine 23-44 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 8281849-6 1994 At the cellular level, 5-aminosalicylic acid inhibited phorbol myristate acetate (100 ng/ml)-activated superoxide generation to 82.3 +/- 9.3%, the formylmethionyl leucyl peptide (10(-5) M) to 61.0 +/- 6.8%, and the NaF (20 mM)-stimulated production to 32.3 +/- 3.2% (mean +/- SD, P < 0.01). Tetradecanoylphorbol Acetate 55-80 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 8281849-6 1994 At the cellular level, 5-aminosalicylic acid inhibited phorbol myristate acetate (100 ng/ml)-activated superoxide generation to 82.3 +/- 9.3%, the formylmethionyl leucyl peptide (10(-5) M) to 61.0 +/- 6.8%, and the NaF (20 mM)-stimulated production to 32.3 +/- 3.2% (mean +/- SD, P < 0.01). Superoxides 103-113 C-X-C motif chemokine ligand 8 Homo sapiens 215-218 8085219-1 1994 Fluoridated toothpicks (John O. Butler Co.), containing an average of 0.80 mg F as NaF, demonstrated a quick F release in vitro after 1 min immersion in distilled water (0.13 mg; 16%). Water 163-168 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 8244994-3 1993 In lipopolysaccharide-stimulated human whole blood, the OH radical scavenger dimethyl sulfoxide (Me2SO) dramatically inhibited (approximately 90%) IL-8 production, but had minimal effects on the production of tumor necrosis factor, interleukin 1 beta (IL-1), and IL-6. oh radical 56-66 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 8244994-3 1993 In lipopolysaccharide-stimulated human whole blood, the OH radical scavenger dimethyl sulfoxide (Me2SO) dramatically inhibited (approximately 90%) IL-8 production, but had minimal effects on the production of tumor necrosis factor, interleukin 1 beta (IL-1), and IL-6. Dimethyl Sulfoxide 77-95 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 8244994-3 1993 In lipopolysaccharide-stimulated human whole blood, the OH radical scavenger dimethyl sulfoxide (Me2SO) dramatically inhibited (approximately 90%) IL-8 production, but had minimal effects on the production of tumor necrosis factor, interleukin 1 beta (IL-1), and IL-6. me2so 97-102 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 8244994-4 1993 To determine whether NADPH-oxidase-generated free radicals were critical in the regulation of IL-8, studies were performed using blood from patients with chronic granulomatous disease. Free Radicals 45-58 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 8244994-5 1993 In both normal individuals and patients with chronic granulomatous disease, production of IL-8 could be initiated with lipopolysaccharide, phytohemagglutinin, or aggregated immune complexes, and this production could be inhibited by Me2SO (1% v/v). me2so 233-238 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 8244994-7 1993 In the human hepatoma cell line Hep-G2, Me2SO dose-dependently inhibited tumor necrosis factor-stimulated IL-8 production, with a 74 +/- 1% reduction observed at a Me2SO concentration of 1%. me2so 40-45 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 8244994-7 1993 In the human hepatoma cell line Hep-G2, Me2SO dose-dependently inhibited tumor necrosis factor-stimulated IL-8 production, with a 74 +/- 1% reduction observed at a Me2SO concentration of 1%. me2so 164-169 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 8244994-8 1993 Direct exposure to ROI demonstrated that H2O2 stimulated IL-8 production in a dose-dependent manner in Hep-G2 cells, A549 pulmonary type II epithelial cells, and human skin fibroblasts; this induction could be prevented by addition of catalase. Hydrogen Peroxide 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 8124912-5 1993 However, a correlation was observed between SF levels of IL-8 with those of lactate, LDH, beta 2-microglobulin and glucose. Lactic Acid 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 8262617-0 1994 Lipoteichoic acid induces secretion of interleukin-8 from human blood monocytes: a cellular and molecular analysis. lipoteichoic acid 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 39-52 8262617-6 1994 The expression of IL-8 mRNA from LTA- but not lipopolysaccharide (LPS)-treated PBM was superinduced by concomitant treatment with cycloheximide, indicating that the expression of IL-8 mRNA from LTA-treated PBM was negatively controlled by repressor proteins. Cycloheximide 130-143 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 8262617-6 1994 The expression of IL-8 mRNA from LTA- but not lipopolysaccharide (LPS)-treated PBM was superinduced by concomitant treatment with cycloheximide, indicating that the expression of IL-8 mRNA from LTA-treated PBM was negatively controlled by repressor proteins. Cycloheximide 130-143 C-X-C motif chemokine ligand 8 Homo sapiens 179-183 8254194-11 1994 However, treatment of monocytes with cycloheximide resulted in the superinduction of IL-8 compared with control monocytes. Cycloheximide 37-50 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 7885789-0 1994 Urine interleukin-6 and interleukin-8 in children with acute pyelonephritis, in relation to DMSA scintigraphy in the acute phase and at 1-year follow-up. Technetium Tc 99m Dimercaptosuccinic Acid 92-96 C-X-C motif chemokine ligand 8 Homo sapiens 24-37 7885789-2 1994 The urine IL-6 and IL-8/creatinine quotients were also related to the urine N-acetyl-beta-D-glucosaminidase (NAG) and albumin/creatinine quotients. Creatinine 126-136 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 7809956-2 1994 Adenylate cyclase sensitivity to sodium inhibition was different upon cyclase stimulation with 1-isoproterenol, Gpp(NH)p and NaF. Sodium 33-39 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 8253721-6 1993 The identical effects of GTP gamma S and NaF suggest that the GTP-sensitive element is a heterotrimeric G-protein. Guanosine Triphosphate 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 8267589-6 1993 Activators of protein kinase C, phorbol myristate acetate (PMA) and 1-oleyl-2-acetyl-sn-glycerol (OAG), inhibited cytosolic Ca(2+)-increase completely when induced by IL-8 and by 68-82% in the case of fMLP. Tetradecanoylphorbol Acetate 32-57 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 8267589-6 1993 Activators of protein kinase C, phorbol myristate acetate (PMA) and 1-oleyl-2-acetyl-sn-glycerol (OAG), inhibited cytosolic Ca(2+)-increase completely when induced by IL-8 and by 68-82% in the case of fMLP. Tetradecanoylphorbol Acetate 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 8267589-6 1993 Activators of protein kinase C, phorbol myristate acetate (PMA) and 1-oleyl-2-acetyl-sn-glycerol (OAG), inhibited cytosolic Ca(2+)-increase completely when induced by IL-8 and by 68-82% in the case of fMLP. 1-oleyl-2-acetyl-sn-glycerol 68-96 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 8267589-6 1993 Activators of protein kinase C, phorbol myristate acetate (PMA) and 1-oleyl-2-acetyl-sn-glycerol (OAG), inhibited cytosolic Ca(2+)-increase completely when induced by IL-8 and by 68-82% in the case of fMLP. 1-oleoyl-2-acetylglycerol 98-101 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 8116830-2 1993 This study was designed to investigate the relationship between chronic alcohol ingestion and cessation with respect to release of interleukin-6 (IL-6) and interleukin-8 (IL-8) using highly specific and sensitive ELISA assays, as well as a functional assay, natural killer cell cytotoxic activity. Alcohols 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 156-169 8116830-2 1993 This study was designed to investigate the relationship between chronic alcohol ingestion and cessation with respect to release of interleukin-6 (IL-6) and interleukin-8 (IL-8) using highly specific and sensitive ELISA assays, as well as a functional assay, natural killer cell cytotoxic activity. Alcohols 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 171-175 8124912-5 1993 However, a correlation was observed between SF levels of IL-8 with those of lactate, LDH, beta 2-microglobulin and glucose. Glucose 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 8138326-4 1993 In the recent past, meta-analytic techniques employed on data concerning > 14,000 clinical trial subjects from 12 studies, have established that the use of NaF in a correctly formulated silica base provides superior caries protection than does either an NaF + SMFP, or SMFP dentifrice. Silicon Dioxide 189-195 C-X-C motif chemokine ligand 8 Homo sapiens 159-162 8244273-0 1993 Production of chemotactic factor, interleukin-8, from hepatocytes exposed to ethanol. Ethanol 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 34-47 8244273-7 1993 These results suggest that a major part of the proteinous chemotactic factors released from hepatocytes exposed to ethanol could be a dimer form of interleukin-8, one of the proinflammatory cytokines, possibly contributing to the pathogenesis of alcoholic hepatitis. Ethanol 115-122 C-X-C motif chemokine ligand 8 Homo sapiens 148-161 8187790-4 1993 Interleukin 8 concentrations increased over time up to 24 h. When LPS was preincubated with teicoplanin (antibiotic: LPS ratio 20:1, w/w), interleukin 8 concentrations were found significantly (p < 0.05) reduced at 4, 8 and 24 h after LPS challenge. Teicoplanin 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8187790-4 1993 Interleukin 8 concentrations increased over time up to 24 h. When LPS was preincubated with teicoplanin (antibiotic: LPS ratio 20:1, w/w), interleukin 8 concentrations were found significantly (p < 0.05) reduced at 4, 8 and 24 h after LPS challenge. Teicoplanin 92-103 C-X-C motif chemokine ligand 8 Homo sapiens 139-152 8187790-6 1993 In this experiment model, a teicoplanin:LPS ratio 100-fold less than the ratio achievable in plasma of septic shock patients was able to reduce interleukin 8, which has been correlated with the severity of septic disease. Teicoplanin 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 144-157 8245474-2 1993 We show that after GM-CSF treatment, the exposure of human neutrophils to IL-8 results in the synthesis of leukotriene (LT)B4 and platelet-activating factor. Leukotrienes 107-118 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 8245474-4 1993 Accordingly, IL-8 induced a substantial release of 3H-arachidonic acid in GM-CSF-treated PMN. 3h-arachidonic acid 51-70 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 8245474-8 1993 Finally, pertussis toxin and the 5-LO translocation inhibitor, MK-886, both blocked the IL-8-elicited 5-LO activation. MK-886 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 8245475-4 1993 Competition binding with 125I-labeled IL-8, however, showed large differences for several of the IL-8 mutants between alpha and beta receptors. Iodine-125 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8245475-4 1993 Competition binding with 125I-labeled IL-8, however, showed large differences for several of the IL-8 mutants between alpha and beta receptors. Iodine-125 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 8245475-10 1993 If the ELR sequence of IL-8 was substituted with alanines or if the carboxyl terminus distal to C50 was replaced with the MGSA sequence, a reduction occurred in binding competition. Alanine 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 8123758-5 1993 Cd, over a wide range of concentrations, did induce human PBMC to produce large amounts of bioactive IL-8, the maximal induction being observed at 10(-4) M. The production was inhibited specifically by a metal chelating agent, ethylenediaminetetraacetic acid (EDTA). Edetic Acid 260-264 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 8123758-0 1993 Cadmium induces interleukin-8 production in human peripheral blood mononuclear cells with the concomitant generation of superoxide radicals. Cadmium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 16-29 8123758-6 1993 Steady level of IL-8 mRNA increased within 30 min after the addition of Cd and reached a maximal level at 2 h, decreasing thereafter. Cadmium 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 8123758-4 1993 Hence, in this study we investigated whether Cd induced IL-8 production in human peripheral blood mononuclear cells (PBMC). Cadmium 45-47 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 8123758-8 1993 Concomitantly with the induction of IL-8, within 10 min Cd generated reactive oxygen intermediates (ROI) in human PBMC. Cadmium 56-58 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 8123758-5 1993 Cd, over a wide range of concentrations, did induce human PBMC to produce large amounts of bioactive IL-8, the maximal induction being observed at 10(-4) M. The production was inhibited specifically by a metal chelating agent, ethylenediaminetetraacetic acid (EDTA). Cadmium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 8123758-5 1993 Cd, over a wide range of concentrations, did induce human PBMC to produce large amounts of bioactive IL-8, the maximal induction being observed at 10(-4) M. The production was inhibited specifically by a metal chelating agent, ethylenediaminetetraacetic acid (EDTA). Edetic Acid 227-258 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 8123758-8 1993 Concomitantly with the induction of IL-8, within 10 min Cd generated reactive oxygen intermediates (ROI) in human PBMC. reactive oxygen intermediates 69-98 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 8123758-10 1993 This notion was also supported by our findings that a superoxide generating agent, paraquat, induced IL-8 production in human PBMC and that NAC blocked this paraquat-induced IL-8 production. Superoxides 54-64 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 8123758-10 1993 This notion was also supported by our findings that a superoxide generating agent, paraquat, induced IL-8 production in human PBMC and that NAC blocked this paraquat-induced IL-8 production. Superoxides 54-64 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 8123758-10 1993 This notion was also supported by our findings that a superoxide generating agent, paraquat, induced IL-8 production in human PBMC and that NAC blocked this paraquat-induced IL-8 production. Paraquat 83-91 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 8123758-10 1993 This notion was also supported by our findings that a superoxide generating agent, paraquat, induced IL-8 production in human PBMC and that NAC blocked this paraquat-induced IL-8 production. Paraquat 83-91 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 8123758-10 1993 This notion was also supported by our findings that a superoxide generating agent, paraquat, induced IL-8 production in human PBMC and that NAC blocked this paraquat-induced IL-8 production. Paraquat 157-165 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 8023744-4 1993 One of the peptides, IL-8(3-25), inhibited the neutrophil chemotactic activity of recombinant IL-8 (rIL-8) which had been preheated to 40 degrees C but did not reduce neutrophil chemokinesis, or the chemotactic activity of unheated rIL-8, FMLP, C5a or LTB4. ril-8 100-105 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 8108182-0 1993 Induction of interleukin-8 expression in neuroblastoma cells by retinoic acid: implication of leukocyte chemotaxis and activation. Tretinoin 64-77 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 8108182-6 1993 RA-treated but not untreated SK-N-SH cells expressed IL-8 mRNA in a time- and dose-dependent fashion. Tretinoin 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 8108182-7 1993 As determined by ELISA, IL-8 levels were detectable in the culture supernatants from RA-treated, but not untreated, neuroblastoma cells (2.65 +/- 0.43 versus 0.05 +/- 0.04 ng/mL). Tretinoin 85-87 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 8108182-10 1993 These results suggest that RA-induced neuroblastoma cell differentiation is associated with production of functional IL-8, which may be involved in the leukocyte infiltration and activation resulting in tumor regression. Tretinoin 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 8304046-1 1993 In this study we tested the effects of sodium fluoride (NaF) in serum-free cultures of human marrow stromal osteoblast-like [hMS(OB)] cells. Sodium Fluoride 39-54 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 8304046-3 1993 NaF alone did not increase type I collagen production, but in the presence of 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] (10(-9) M), NaF enhanced type I collagen production in a dose-dependent way to 300% of 1,25-(OH)2D3-treated control cultures. 1,25-dihydroxyvitamin d3 [1,25-(oh)2d3 78-116 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 8304046-3 1993 NaF alone did not increase type I collagen production, but in the presence of 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] (10(-9) M), NaF enhanced type I collagen production in a dose-dependent way to 300% of 1,25-(OH)2D3-treated control cultures. Calcitriol 104-116 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 8023744-4 1993 One of the peptides, IL-8(3-25), inhibited the neutrophil chemotactic activity of recombinant IL-8 (rIL-8) which had been preheated to 40 degrees C but did not reduce neutrophil chemokinesis, or the chemotactic activity of unheated rIL-8, FMLP, C5a or LTB4. ril-8 100-105 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 7988766-0 1993 Fluoride release in vitro from various glass ionomer cements and resin composites after exposure to NaF solutions. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 7988766-8 1993 After exposure to NaF, the fluoride release was significantly higher for the silver cermet material than for the other glass ionomers tested. Fluorides 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 7988766-8 1993 After exposure to NaF, the fluoride release was significantly higher for the silver cermet material than for the other glass ionomers tested. silver cermet 77-90 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 8214944-4 1993 Therefore, we conducted a prospective study in order to investigate whether methylprednisolone (MP) pretreatment (30 mg/kg) could influence the appearance of IL-8 (a recently discovered cytokine with potent neutrophil-chemotactic activity) in the peripheral circulation. Methylprednisolone 76-94 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 8406851-9 1993 Moreover, the presence of a primed subpopulation of blood PMN with respect to H2O2 production indicates that IL-8 may contribute to the neutrophil-mediated process in the pathogenesis of ARDS and pneumonia. Hydrogen Peroxide 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 8413306-1 1993 The interleukin-8 promoter is transcriptionally activated by interleukin-1, tumor necrosis factor alpha, phorbol myristate acetate, or hepatitis B virus X protein through a sequence located between positions -91 and -71. Tetradecanoylphorbol Acetate 105-130 C-X-C motif chemokine ligand 8 Homo sapiens 4-17 8400299-10 1993 In leukemic cells expressing the IL-8 receptor, IL-8 induced cytosolic free calcium changes, indicating activation of the classical signaling pathway. Calcium 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 8400299-10 1993 In leukemic cells expressing the IL-8 receptor, IL-8 induced cytosolic free calcium changes, indicating activation of the classical signaling pathway. Calcium 76-83 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 8400301-9 1993 IL-8 caused a rapid increase in neutrophil intracellular calcium that could be completely inhibited by the chelating agent 1,2-bis(o-aminophenoxy)ethane-N,N-N",N"-tetraacetic acid (BAPTA). Calcium 57-64 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8400301-9 1993 IL-8 caused a rapid increase in neutrophil intracellular calcium that could be completely inhibited by the chelating agent 1,2-bis(o-aminophenoxy)ethane-N,N-N",N"-tetraacetic acid (BAPTA). 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid 123-179 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8400301-9 1993 IL-8 caused a rapid increase in neutrophil intracellular calcium that could be completely inhibited by the chelating agent 1,2-bis(o-aminophenoxy)ethane-N,N-N",N"-tetraacetic acid (BAPTA). 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid 181-186 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8400301-10 1993 However, BAPTA-treated neutrophils retained the ability to increase F-actin in response to IL-8. 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid 9-14 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 8400301-11 1993 Similar results were seen with fMLP, indicating that, similar to fMLP, the IL-8-induced actin response is mediated through pertussis-toxin-sensitive G-proteins but is neither dependent on PKC nor increases in cytosolic calcium. Calcium 219-226 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 7694480-3 1993 In particular, we assessed whether dexamethasone was capable of inhibiting the tumor necrosis factor-alpha (TNF-alpha)-mediated secretion of interleukin-6 (IL-6), interleukin-8 (IL-8), and granulocyte colony-stimulating factor (G-CSF) by a human bronchial epithelial cell line (BEAS-2B). Dexamethasone 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 163-176 7694480-3 1993 In particular, we assessed whether dexamethasone was capable of inhibiting the tumor necrosis factor-alpha (TNF-alpha)-mediated secretion of interleukin-6 (IL-6), interleukin-8 (IL-8), and granulocyte colony-stimulating factor (G-CSF) by a human bronchial epithelial cell line (BEAS-2B). Dexamethasone 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 178-182 7694480-7 1993 Although dexamethasone appeared to reduce both the secretion of immunoreactive IL-8 and accumulation of IL-8 mRNA, the inhibitory effects did not reach statistical significance. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 7694480-7 1993 Although dexamethasone appeared to reduce both the secretion of immunoreactive IL-8 and accumulation of IL-8 mRNA, the inhibitory effects did not reach statistical significance. Dexamethasone 9-22 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 29016269-6 1993 In the presence of NaCl, Na2SO4, MgClg, CaCl2, NaF and urea, the adsorption was slightly affected. Sodium Chloride 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 29016269-6 1993 In the presence of NaCl, Na2SO4, MgClg, CaCl2, NaF and urea, the adsorption was slightly affected. sodium sulfate 25-31 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 8228330-13 1993 Cycloheximide treatment blocked this IL-8 protein induction. Cycloheximide 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 7902747-3 1993 Noradrenaline-, ATP-, histamine- and glutamate-evoked [3H]-inositol phosphate accumulations were potentiated to varying degrees in PKC-depleted cultures whilst those evoked by carbachol and NaF were reduced and unchanged respectively. Norepinephrine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 190-193 7902747-3 1993 Noradrenaline-, ATP-, histamine- and glutamate-evoked [3H]-inositol phosphate accumulations were potentiated to varying degrees in PKC-depleted cultures whilst those evoked by carbachol and NaF were reduced and unchanged respectively. Adenosine Triphosphate 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 190-193 7902747-3 1993 Noradrenaline-, ATP-, histamine- and glutamate-evoked [3H]-inositol phosphate accumulations were potentiated to varying degrees in PKC-depleted cultures whilst those evoked by carbachol and NaF were reduced and unchanged respectively. Histamine 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 190-193 7902747-3 1993 Noradrenaline-, ATP-, histamine- and glutamate-evoked [3H]-inositol phosphate accumulations were potentiated to varying degrees in PKC-depleted cultures whilst those evoked by carbachol and NaF were reduced and unchanged respectively. Glutamic Acid 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 190-193 7691110-9 1993 Rhamnolipids and MEP were found to stimulate the copious release of IL-8, GM-CSF, and IL-6 from epithelial cells, in a steroid-sensitive fashion. Steroids 119-126 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 8214944-4 1993 Therefore, we conducted a prospective study in order to investigate whether methylprednisolone (MP) pretreatment (30 mg/kg) could influence the appearance of IL-8 (a recently discovered cytokine with potent neutrophil-chemotactic activity) in the peripheral circulation. Methylprednisolone 96-98 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 8413215-4 1993 A nuclear complex was induced in phorbol myristate acetate-treated Jurkat T cells which bound specifically to the kappa B site of the IL-8 promoter and was inhibited by addition of purified I kappa B alpha to the reaction mixture. Tetradecanoylphorbol Acetate 33-58 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 8413215-10 1993 Antisense oligonucleotides to RelA, but not NFKB1, inhibited phorbol myristate acetate-induced IL-8 production in Jurkat T lymphocytes. Oligonucleotides 10-26 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 8413215-10 1993 Antisense oligonucleotides to RelA, but not NFKB1, inhibited phorbol myristate acetate-induced IL-8 production in Jurkat T lymphocytes. Tetradecanoylphorbol Acetate 61-86 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 8219478-8 1993 IL-8 was not influenced by GH or IGF-I, was slightly but not significantly increased by PTH(1-34) and was reduced by 1,25(OH)2D3 and 17 beta-oestradiol at supraphysiological doses. beta-oestradiol 136-151 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8399143-7 1993 On the basis of the conservation of four cysteine residues, the two molecules are to be classified within the C-X-C chemokine family, including IL-8. Cysteine 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 8103045-2 1993 We have previously demonstrated that a basic amino acid residue of interleukin (IL)-8, namely Arg-6, is critical for the binding of IL-8 to its receptor. Amino Acids, Basic 39-55 C-X-C motif chemokine ligand 8 Homo sapiens 67-85 8103045-2 1993 We have previously demonstrated that a basic amino acid residue of interleukin (IL)-8, namely Arg-6, is critical for the binding of IL-8 to its receptor. Amino Acids, Basic 39-55 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 8103045-2 1993 We have previously demonstrated that a basic amino acid residue of interleukin (IL)-8, namely Arg-6, is critical for the binding of IL-8 to its receptor. Arginine 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 67-85 8103045-2 1993 We have previously demonstrated that a basic amino acid residue of interleukin (IL)-8, namely Arg-6, is critical for the binding of IL-8 to its receptor. Arginine 94-97 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 8103045-4 1993 To identify this key residue, we systematically mutated to Ala all acidic residues present on the ligand accessible surface of IL-8 receptor type A. Alanine 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 8103045-7 1993 These data suggest that Lys-11 recruits a new and favorable interaction with IL-8 (analogous to that of IL-8 receptor type B with IL-8) or that the cavity created by mutating Asp-11 to Ala is particularly deleterious. lys-11 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 8103045-7 1993 These data suggest that Lys-11 recruits a new and favorable interaction with IL-8 (analogous to that of IL-8 receptor type B with IL-8) or that the cavity created by mutating Asp-11 to Ala is particularly deleterious. lys-11 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 8103045-7 1993 These data suggest that Lys-11 recruits a new and favorable interaction with IL-8 (analogous to that of IL-8 receptor type B with IL-8) or that the cavity created by mutating Asp-11 to Ala is particularly deleterious. lys-11 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 7488352-1 1993 The 10 pivotal caries clinical studies employed in a recent meta-analysis to compare the anticaries efficacy of sodium fluoride (NaF) and sodium monofluorophosphate (MFP) dentifrices were subjected to a critical review. Sodium Fluoride 112-127 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 8142610-6 1993 However, PQ potentiated the production of IL-8 in the presence of 1 ng/ml of endotoxin (lipopolysaccharide, LPS). Paraquat 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 7488354-1 1993 The comparison of the anticaries efficacy of dentifrices containing sodium fluoride (NaF) and sodium monofluorophosphate (SMFP) has recently been addressed through a meta-analysis of published head-to-head clinical trials. Sodium Fluoride 68-83 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 8396851-5 1993 RESULTS: Significant quantities of interleukin-8 were produced by the tissue, and the data indicate that cervical explants from pregnant and nonpregnant women behave in a similar way when challenged by phorbol myristate acetate but that the postmenopausal cervix loses its capacity for interleukin-8 production. Tetradecanoylphorbol Acetate 202-227 C-X-C motif chemokine ligand 8 Homo sapiens 35-48 8396851-6 1993 CONCLUSIONS: Human cervix is capable of producing large amounts of interleukin-8 in vitro, and it may be influenced by the steroid hormones. Steroids 123-139 C-X-C motif chemokine ligand 8 Homo sapiens 67-80 8396001-8 1993 LTB4, IL-8, and PLA2 levels were elevated in patients with NIP; LTB4 and PLA2 levels correlated with absolute neutrophil count, and IL-8 correlated with alveolar-arterial oxygen pressure difference. Oxygen 171-177 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 8142610-0 1993 The pneumotoxicant paraquat induces IL-8 mRNA in human mononuclear cells and pulmonary epithelial cells. Paraquat 19-27 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 8142610-3 1993 We have studied the effect of PQ on the expression of the neutrophil chemotactic cytokine, IL-8, by human peripheral blood mononuclear cells (PBMC). Paraquat 30-32 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 8216423-8 1993 We confirmed that the majority of the neutrophil-stimulating activity was IL-8 by 3 different approaches: cross-desensitization experiments with IL-8, melanoma growth-stimulatory activity, and neutrophil-activating peptide 2, stimulation of calcium mobilization in cells transfected with the IL-8 receptor complementary DNA, and inhibition of the activity following pretreatment of the supernatants with an anti-IL-8 antibody. Calcium 241-248 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 8142610-8 1993 Stimulation of IL-8 mRNA by PQ was suppressed by IL-4 and by free radical scavengers (dimethylsulfoxide, mannitol). Paraquat 28-30 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 8142610-5 1993 While PQ did stimulate the appearance of IL-8 mRNA, no significant production of IL-8 protein was detected. Paraquat 6-8 C-X-C motif chemokine ligand 8 Homo sapiens 41-45 8142610-8 1993 Stimulation of IL-8 mRNA by PQ was suppressed by IL-4 and by free radical scavengers (dimethylsulfoxide, mannitol). Dimethyl Sulfoxide 86-103 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 8142610-8 1993 Stimulation of IL-8 mRNA by PQ was suppressed by IL-4 and by free radical scavengers (dimethylsulfoxide, mannitol). Mannitol 105-113 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 8142610-9 1993 Increased IL-8 expression by PQ was also observed in the human pulmonary epithelial cell line A549 indicating that the effect of PQ was not specific for PBMC. Paraquat 29-31 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 8142610-9 1993 Increased IL-8 expression by PQ was also observed in the human pulmonary epithelial cell line A549 indicating that the effect of PQ was not specific for PBMC. Paraquat 129-131 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 8142610-10 1993 These findings suggest that IL-8 might be involved in the pulmonary effects of PQ and that its production might be stimulated following an oxidative insult, and might clarify the pathogenetic mechanisms of adult respiratory distress syndrome (ARDS) or oxidant-induced pulmonary fibrosis. Paraquat 79-81 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 8342895-9 1993 In addition, CSR-CSA cycle length correlated with LECT (r = 0.939, p < 0.001). Cyclosporine 17-20 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 8359798-7 1993 The alcohol-dependent control group and the normal volunteer controls had mean interleukin-8 concentrations of 106 +/- 28 pg/ml and 10 +/- 5 pg/ml, respectively. Alcohols 4-11 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 8245177-1 1993 In human monocytes phorbol-12-myristate 13-acetate (PMA) did not induce IL-6 but it increased IL-1 beta and IL-8 mRNA levels. Tetradecanoylphorbol Acetate 19-50 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 8245177-1 1993 In human monocytes phorbol-12-myristate 13-acetate (PMA) did not induce IL-6 but it increased IL-1 beta and IL-8 mRNA levels. Tetradecanoylphorbol Acetate 52-55 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 8360485-9 1993 Exposure of the two melanoma cell lines in vitro to antisense oligonucleotides targeted against two different sites of human IL-8 mRNA-inhibited cell proliferation, colony formation in soft agar, and secretion of IL-8 protein into culture supernatant in a dose dependent fashion. Oligonucleotides 62-78 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 8360485-9 1993 Exposure of the two melanoma cell lines in vitro to antisense oligonucleotides targeted against two different sites of human IL-8 mRNA-inhibited cell proliferation, colony formation in soft agar, and secretion of IL-8 protein into culture supernatant in a dose dependent fashion. Oligonucleotides 62-78 C-X-C motif chemokine ligand 8 Homo sapiens 213-217 8345201-13 1993 Interestingly, in contrast to the regulation of monocyte-derived IL-8 by PGE2, PGE2 treatment of PMN failed to inhibit the generation of LPS-induced IL-8. Dinoprostone 73-77 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 8345201-7 1993 Because PMN and monocytes share the same stem cell, and monocyte-derived IL-8 is regulated by prostaglandin E2 (PGE2), glucocorticoids (dexamethasone; DEX) and the T-Lymphocyte-derived IL-4, we postulated that PMN-derived IL-8 production may be regulated in a similar manner. Dinoprostone 94-110 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 8345201-7 1993 Because PMN and monocytes share the same stem cell, and monocyte-derived IL-8 is regulated by prostaglandin E2 (PGE2), glucocorticoids (dexamethasone; DEX) and the T-Lymphocyte-derived IL-4, we postulated that PMN-derived IL-8 production may be regulated in a similar manner. Dinoprostone 112-116 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 8345201-7 1993 Because PMN and monocytes share the same stem cell, and monocyte-derived IL-8 is regulated by prostaglandin E2 (PGE2), glucocorticoids (dexamethasone; DEX) and the T-Lymphocyte-derived IL-4, we postulated that PMN-derived IL-8 production may be regulated in a similar manner. Dexamethasone 136-149 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 8345201-7 1993 Because PMN and monocytes share the same stem cell, and monocyte-derived IL-8 is regulated by prostaglandin E2 (PGE2), glucocorticoids (dexamethasone; DEX) and the T-Lymphocyte-derived IL-4, we postulated that PMN-derived IL-8 production may be regulated in a similar manner. Dextromethorphan 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 8345201-11 1993 DEX and IL-4 in concentrations of 10(-6) M and 10 ng/ml resulted in maximal inhibition of LPS-induced PMN-derived IL-8, respectively. Dextromethorphan 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 8345201-12 1993 Moreover, both DEX and IL-4 administration could be delayed 4 hr post-stimulation with LPS and result in significant suppression of PMN-derived IL-8. Dextromethorphan 15-18 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 8394087-3 1993 Detailed analysis of phorbol 12-myristate 13-acetate-treated THP-1 cells showed an increased PBR expression and the rise came along with an increase of CD11a and CD11b antigens and a secretion of macrophagic cytokines tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-1 beta and IL-8. Tetradecanoylphorbol Acetate 21-52 C-X-C motif chemokine ligand 8 Homo sapiens 287-291 8162335-0 1993 ETH615, a synthetic inhibitor of leukotriene biosynthesis and function, also inhibits the production of and biological responses towards interleukin-8. ETH 615 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 137-150 8105874-3 1993 Apart from G-CSF, IL-8 was the weakest priming agent and was weaker than GM-CSF in priming arachidonic acid metabolism stimulated by calcium ionophore. Arachidonic Acid 91-107 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 8105874-3 1993 Apart from G-CSF, IL-8 was the weakest priming agent and was weaker than GM-CSF in priming arachidonic acid metabolism stimulated by calcium ionophore. Calcium 133-140 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 8162335-6 1993 These results further support the concept of a cytokine-leukotriene regulatory circuit and encourage the establishment of clinical trials testing the effect of ETH615 on inflammatory skin diseases, which are characterized by high levels of interleukin-8 and leukotriene B4 in lesional skin. ETH 615 160-166 C-X-C motif chemokine ligand 8 Homo sapiens 240-253 8162335-0 1993 ETH615, a synthetic inhibitor of leukotriene biosynthesis and function, also inhibits the production of and biological responses towards interleukin-8. Leukotrienes 33-44 C-X-C motif chemokine ligand 8 Homo sapiens 137-150 8162335-1 1993 ETH615 (4-(2-quinolylmethoxy)-N-(3-fluorobenzyl-phenyl-amino-methyl -4- benzoic-acid), a synthetic inhibitor of leukotriene B4 production and activities, was tested for its effect on the production of and biological responses towards human interleukin-8. ETH 615 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 240-253 8162335-2 1993 We found that ETH615 inhibits lipopolysaccharide-induced (LPS-induced) expression of interleukin-8 messenger-RNA (mRNA) and interleukin-8 production in human peripheral blood mononuclear cells. ETH 615 14-20 C-X-C motif chemokine ligand 8 Homo sapiens 85-98 8162335-2 1993 We found that ETH615 inhibits lipopolysaccharide-induced (LPS-induced) expression of interleukin-8 messenger-RNA (mRNA) and interleukin-8 production in human peripheral blood mononuclear cells. ETH 615 14-20 C-X-C motif chemokine ligand 8 Homo sapiens 124-137 8162335-3 1993 We also observed that ETH615 completely inhibited interleukin-8 as well as leukotriene B4 directed chemotaxis of human neutrophils in a dose-dependent manner. ETH 615 22-28 C-X-C motif chemokine ligand 8 Homo sapiens 50-63 8406585-0 1993 Interleukin-8 primes human neutrophils for enhanced superoxide anion production. Superoxides 52-68 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8406585-2 1993 In this study, we investigated the effect of recombinant human (rh) IL-8 on superoxide (O2-) production by neutrophils. Superoxides 76-86 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 8406585-2 1993 In this study, we investigated the effect of recombinant human (rh) IL-8 on superoxide (O2-) production by neutrophils. Superoxides 88-90 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 8406585-5 1993 Recombinant human IL-8 increased both the maximal rate and the total O2- production, but did not prolong the response to FMLP. Superoxides 69-71 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 8335925-7 1993 The levels of MCP-1 and IL-8 protein from mixed lymphocyte reaction supernatants as measured by specific ELISA were positively correlated with the proliferative response as measured by [3H]TdR uptake. Tritium 186-188 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 8335897-3 1993 In this study we tested the hypothesis that RPM-mediated therapeutic effects on accelerated rejection may be linked to decreased expression of protein encoded by gro/melanoma-growth stimulatory activity gene (KC) and macrophage inflammatory protein-2 (MIP-2) genes, the operational rat homologues of the human intercrine-alpha cytokines with proinflammatory IL-8-like neutrophil activation/chemotactic properties. Sirolimus 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 358-362 8346230-0 1993 Binding to heparan sulfate or heparin enhances neutrophil responses to interleukin 8. Heparitin Sulfate 11-26 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 8346230-0 1993 Binding to heparan sulfate or heparin enhances neutrophil responses to interleukin 8. Heparin 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 71-84 8346230-1 1993 The interaction of interleukin 8 (IL-8) with heparin was studied by using synthetic IL-8 analogs with C- and N-terminal truncations. Heparin 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 19-32 8346230-1 1993 The interaction of interleukin 8 (IL-8) with heparin was studied by using synthetic IL-8 analogs with C- and N-terminal truncations. Heparin 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 8346230-5 1993 When IL-8 was applied together with heparan sulfate, neutrophil chemotaxis in vitro was enhanced up to 4-fold, and the stimulus-dependent increase in cytosolic free Ca2+ increased markedly in both rate and peak value. Heparitin Sulfate 36-51 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 8346230-10 1993 Taken together, these results suggest that heparan sulfate, which is present on the endothelial cell surface and in the basement membrane, may have a dual function in diapedesis, promotion of IL-8-dependent transmigration of neutrophils, and protection of the tissue microenvironment from damage by lytic enzymes released from the migrating cells. Heparitin Sulfate 43-58 C-X-C motif chemokine ligand 8 Homo sapiens 192-196 8335923-2 1993 For example, after exposure to the inflammatory particulate stimulus zymosan (or its derivative beta 1,3-glucan), monocyte/macrophages synthesize and release lysosomal hydrolases, mobilize arachadonic acid, and secrete cytokines such as TNF-alpha and IL-8. Zymosan 69-76 C-X-C motif chemokine ligand 8 Homo sapiens 251-255 8360592-4 1993 RA differentially modulated the expression of interleukin-1 beta (IL-1 beta), IL-6, and IL-8 mRNAs depending on the inducing stimulus. Tretinoin 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 8360592-5 1993 While phorbol myristate acetate-induced IL-1 beta and IL-8 mRNA expression was increased by RA (IL-6 could not be induced by this pathway in monocytes), IL-1 beta-induced expression of IL-1 beta and IL-8 was markedly reduced and IL-6 gene expression was almost completely suppressed. Tetradecanoylphorbol Acetate 6-31 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 8393671-1 1993 NaF stimulation produces a strong dichlorofluorescin (DCFH) dye oxidation signal in HL-60 and PLB-985 human myeloid leukemia cells. 2',7'-dichlorofluorescein 34-52 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8393671-1 1993 NaF stimulation produces a strong dichlorofluorescin (DCFH) dye oxidation signal in HL-60 and PLB-985 human myeloid leukemia cells. DCFH 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8393671-4 1993 NaF-stimulated DCFH oxidation appears to occur via a pathway that is distinct from respiratory burst oxidant-mediated DCFH oxidation. DCFH 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8335897-11 1993 In contrast, the allografts from RPM-treated hosts showed essentially no neutrophil infiltration and minor, focal staining for IL-8 and IFN-gamma. Sirolimus 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 8397092-2 1993 Histamine (EC50 6.5 microM), bradykinin (EC50 9.7 nM), carbachol (EC50 10 microM), substance P and NaF all produced concentration dependent [3H]inositol phosphate formation in these cells. Tritium 141-143 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 8397092-2 1993 Histamine (EC50 6.5 microM), bradykinin (EC50 9.7 nM), carbachol (EC50 10 microM), substance P and NaF all produced concentration dependent [3H]inositol phosphate formation in these cells. Inositol Phosphates 144-162 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 8335897-13 1993 It also documents a novel effect of RPM in vivo, which results in the suppression of intragraft IL-8-like and CTL-dependent mRNA/protein production and diminished neutrophil infiltration; these may contribute to the striking efficacy of RPM therapy in sensitized graft recipients. Sirolimus 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 8335897-13 1993 It also documents a novel effect of RPM in vivo, which results in the suppression of intragraft IL-8-like and CTL-dependent mRNA/protein production and diminished neutrophil infiltration; these may contribute to the striking efficacy of RPM therapy in sensitized graft recipients. Sirolimus 237-240 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 8335079-6 1993 Furthermore, native IL-8 was found to specifically bind CsA, whereas biologically inactive analogs of CsA were not bound by IL-8. Cyclosporine 56-59 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 8319811-0 1993 Calcium ionophore A23187 induces interleukin-8 gene expression and protein secretion in human monocytic cells. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 8335079-7 1993 Putative binding sites for CsA on IL-8 could be identified on the basis of structural similarities between IL-8 and cyclophilin. Cyclosporine 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 8319811-0 1993 Calcium ionophore A23187 induces interleukin-8 gene expression and protein secretion in human monocytic cells. Calcimycin 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 8335079-7 1993 Putative binding sites for CsA on IL-8 could be identified on the basis of structural similarities between IL-8 and cyclophilin. Cyclosporine 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 8335079-9 1993 We conclude that the specific binding of CsA to IL-8 may explain some of the anti-inflammatory effects of CsA. Cyclosporine 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 8319811-3 1993 Bacterial lipopolysaccharide endotoxin (LPS) or phorbol myristate acetate (PMA) alone induced suboptimal expression as assessed by Northern blotting; however, preincubation of cells with PMA followed by endotoxin induced much higher levels of IL-8 mRNA. lipopolysaccharide endotoxin 10-38 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 8391481-0 1993 Functions of interleukin-8 are mediated through thiol group(s) of IL-8 receptor in human polymorphonuclear neutrophils. Sulfhydryl Compounds 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 13-26 8319811-3 1993 Bacterial lipopolysaccharide endotoxin (LPS) or phorbol myristate acetate (PMA) alone induced suboptimal expression as assessed by Northern blotting; however, preincubation of cells with PMA followed by endotoxin induced much higher levels of IL-8 mRNA. Tetradecanoylphorbol Acetate 48-73 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 8335079-9 1993 We conclude that the specific binding of CsA to IL-8 may explain some of the anti-inflammatory effects of CsA. Cyclosporine 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 8319811-3 1993 Bacterial lipopolysaccharide endotoxin (LPS) or phorbol myristate acetate (PMA) alone induced suboptimal expression as assessed by Northern blotting; however, preincubation of cells with PMA followed by endotoxin induced much higher levels of IL-8 mRNA. Tetradecanoylphorbol Acetate 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 8391481-0 1993 Functions of interleukin-8 are mediated through thiol group(s) of IL-8 receptor in human polymorphonuclear neutrophils. Sulfhydryl Compounds 48-53 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 8391481-1 1993 Effects of 5,5"-dithio-bis(2-nitrobenzoic acid) on IL-8 receptor. Dithionitrobenzoic Acid 11-47 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 8319811-3 1993 Bacterial lipopolysaccharide endotoxin (LPS) or phorbol myristate acetate (PMA) alone induced suboptimal expression as assessed by Northern blotting; however, preincubation of cells with PMA followed by endotoxin induced much higher levels of IL-8 mRNA. Tetradecanoylphorbol Acetate 187-190 C-X-C motif chemokine ligand 8 Homo sapiens 243-247 8326131-5 1993 This antiserum was found to block, in a dose-dependent manner, 1) zymosan-induced neutrophil chemotaxis, 2) C5a-induced enzyme release from neutrophils, and 3) C5a-induced cytokine production (IL-6 and IL-8) from human monocytes in vitro. Zymosan 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 8319811-4 1993 Incubation of the cells with the calcium ionophore A23187 resulted in consistent increased IL-8 gene expression comparable to that of cells treated with endotoxin alone. Calcium 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 8319811-4 1993 Incubation of the cells with the calcium ionophore A23187 resulted in consistent increased IL-8 gene expression comparable to that of cells treated with endotoxin alone. Calcimycin 51-57 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 8319811-5 1993 In addition to inducing IL-8 mRNA this calcium ionophore also induced IL-8 protein synthesis as assessed by immunofluorescence and secretion as detected by ELISA. Calcium 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 8319811-5 1993 In addition to inducing IL-8 mRNA this calcium ionophore also induced IL-8 protein synthesis as assessed by immunofluorescence and secretion as detected by ELISA. Calcium 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 8319811-6 1993 These results indicate that increases in intracellular calcium result in IL-8 gene expression and protein secretion. Calcium 55-62 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 8391481-5 1993 Treatment of neutrophils with 5,5"-dithio-bis(2-nitrobenzoic acid), a thiol-specific modifier, at the concentrations of 0.4 mM and 1 mM reduced IL-8 binding ability and IL-8-induced migration of the cells by 45% and 65%, respectively. Dithionitrobenzoic Acid 30-65 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 8391481-5 1993 Treatment of neutrophils with 5,5"-dithio-bis(2-nitrobenzoic acid), a thiol-specific modifier, at the concentrations of 0.4 mM and 1 mM reduced IL-8 binding ability and IL-8-induced migration of the cells by 45% and 65%, respectively. Dithionitrobenzoic Acid 30-65 C-X-C motif chemokine ligand 8 Homo sapiens 169-173 8391481-5 1993 Treatment of neutrophils with 5,5"-dithio-bis(2-nitrobenzoic acid), a thiol-specific modifier, at the concentrations of 0.4 mM and 1 mM reduced IL-8 binding ability and IL-8-induced migration of the cells by 45% and 65%, respectively. Sulfhydryl Compounds 70-75 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 8391481-7 1993 All the evidence suggests that one or more critical thiol residues are located in the IL-8 binding site of the receptor which are indispensible for normal functions of IL-8. Sulfhydryl Compounds 52-57 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 8391481-7 1993 All the evidence suggests that one or more critical thiol residues are located in the IL-8 binding site of the receptor which are indispensible for normal functions of IL-8. Sulfhydryl Compounds 52-57 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 7686853-4 1993 In terms of maximal adherence inhibition, a rank list was found in the order of N-formyl-Met-Leu-Phe > C5adesArg > interleukin-8 > C5a > or = leukotriene B4, whereas platelet-activating factor, and lipopolysaccharide showed no inhibition. N-Formylmethionine Leucyl-Phenylalanine 80-100 C-X-C motif chemokine ligand 8 Homo sapiens 121-134 8325620-5 1993 In contrast, moderate elevations in the levels of circulating interleukin-8 were seen in alcoholic cirrhosis (geometric mean = 93 ng/L; confidence interval = 40 to 213) and in alcoholic patients undergoing alcohol withdrawal (geometric mean = 137 ng/L; confidence interval = 72 to 259). Alcohols 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 62-75 8336074-3 1993 Lung giant cell carcinoma-derived chemotactic protein (LUCT)/IL-8 and fMet-Leu-Phe stimulate phosphorylation of a 64-kd protein (p64) in 32P-labeled human polymorphonuclear leukocytes (PMNs). Phosphorus-32 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 0-53 8336074-3 1993 Lung giant cell carcinoma-derived chemotactic protein (LUCT)/IL-8 and fMet-Leu-Phe stimulate phosphorylation of a 64-kd protein (p64) in 32P-labeled human polymorphonuclear leukocytes (PMNs). Phosphorus-32 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 8323978-0 1993 Characterization of interleukin-8 receptors in human neutrophil membranes: regulation by guanine nucleotides. Guanine Nucleotides 89-108 C-X-C motif chemokine ligand 8 Homo sapiens 20-33 8336074-3 1993 Lung giant cell carcinoma-derived chemotactic protein (LUCT)/IL-8 and fMet-Leu-Phe stimulate phosphorylation of a 64-kd protein (p64) in 32P-labeled human polymorphonuclear leukocytes (PMNs). Phosphorus-32 137-140 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 8371232-5 1993 Before the treatment with colchicine, the neutrophil chemotactic and activating peptide, interleukin 8 (IL-8), was the major neutrophil chemotaxin within the SF. Colchicine 26-36 C-X-C motif chemokine ligand 8 Homo sapiens 89-102 8371232-5 1993 Before the treatment with colchicine, the neutrophil chemotactic and activating peptide, interleukin 8 (IL-8), was the major neutrophil chemotaxin within the SF. Colchicine 26-36 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 8371232-7 1993 Our data indicate that IL-8 was the major neutrophil chemotaxin in the SF, and that while the condition was alleviated with colchicine, the underlying disorder still existed, with the potential that discontinuance of the colchicine would result in the unrestrained action of the IL-8. Colchicine 221-231 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 8503562-0 1993 Changes in cell population and tumor necrosis factor, interleukin-6, and interleukin-8 in malignant pleural effusions after treatment with intrapleural tetracycline. Tetracycline 152-164 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 8503562-8 1993 The results suggest that TC intrapleural injection induces the release of cytokines (IL-6 and TNF), which are markers of an inflammatory response, and releases IL-8, which attracts neutrophils into the pleural space, which may be the mechanism of the sclerosing effect of TC. Tetracycline 25-27 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 8506955-7 1993 Stimulation of HPMC with combinations of IL-1 beta and TNF-alpha resulted in a synergistic increase in IL-8 release. hydroxypropylmethylcellulose-lactose matrix 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 8506955-10 1993 These data demonstrate that HPMC synthesize IL-8 and that its release can be regulated as a result of induction of mRNA expression and de novo protein synthesis by other cytokines. hydroxypropylmethylcellulose-lactose matrix 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 8347559-3 1993 The binding of 125I-labeled rabbit IL-8 to rabbit neutrophils was inhibited by unlabeled human IL-8 as well as rabbit IL-8 but not by another leucocyte chemotactic cytokine (chemokine), monocyte chemotactic and activating factor. Iodine-125 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 8393062-4 1993 32P-Labeled PMNs were stimulated with LUCT/IL-8, fMLP, leukotriene B4, or C5a, and phosphorylated proteins were analyzed by two-dimensional electrophoresis and autoradiography. Phosphorus-32 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8396484-7 1993 The IP formation elicited by NaF was inhibited by PMA and octylindolactam V with a comparable IC50 value of 7.5 nM while was unchanged after ATP pretreatment. Adenosine Triphosphate 141-144 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 8358540-18 1993 The EC50 value for NaF-stimulated IPn accumulation in control cells was 10.5 +/- 1.1 mm and the maximum response was 136 +/- 41% over basal after 20 min incubation. isoamyl nitrite 34-37 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 8358540-19 1993 In histamine desensitized HeLa cells the EC50 value for NaF was 12.3 +/- 0.4 mM after 20 min stimulation,which was not significantly different from the value obtained in control cells. Histamine 3-12 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 8358540-20 1993 The maximum NaF stimulated IPn formation in desensitized cells of 68 +/- 23% over basal occurred at 15 -20 mM and was significantly lower (P<0.01) than that obtained in control cells.7. isoamyl nitrite 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 8344709-5 1993 The intradermal injection of recombinant human (rh)IL-8 induced a dose-dependent accumulation of intravenously administered [111In]eosinophils into the skin sites over 4 hr. Indium-111 125-130 C-X-C motif chemokine ligand 8 Homo sapiens 51-55 8323978-3 1993 The present study characterizes IL-8 receptors in isolated PMN membrane fractions and shows direct regulation of these receptors by guanine nucleotides. Guanine Nucleotides 132-151 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 8323978-9 1993 Treatment of membranes with the nonhydrolyzable analogs of GTP, GMP-PNP and GTP gamma S, inhibited the binding of [125I]IL-8. Guanosine Triphosphate 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 8323978-9 1993 Treatment of membranes with the nonhydrolyzable analogs of GTP, GMP-PNP and GTP gamma S, inhibited the binding of [125I]IL-8. Guanylyl Imidodiphosphate 64-71 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 8323978-9 1993 Treatment of membranes with the nonhydrolyzable analogs of GTP, GMP-PNP and GTP gamma S, inhibited the binding of [125I]IL-8. Guanosine Triphosphate 76-79 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 8323978-10 1993 GMP-PNP decreased the affinity of the IL-8 receptor by approx. Guanylyl Imidodiphosphate 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8496597-0 1993 Differential action of cycloheximide and activation stimuli on transcription of tumor necrosis factor-alpha, IL-1 beta, IL-8, and P53 genes in human monocytes. Cycloheximide 23-36 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 8323978-12 1993 These findings demonstrate that IL-8 receptors in PMN membranes are of high affinity and are convertible to a low-affinity state in the presence of guanine nucleotides, suggesting a direct role for G proteins in transmembrane signaling by this cytokine. Guanine Nucleotides 148-167 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 8490165-8 1993 IL-8 synthesis after aspirin ingestion was inhibited by 90% (P < .01) as compared with the preaspirin stimulation. Aspirin 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 8367538-5 1993 This effect was qualitatively similar to that induced by NaF, suggesting that quercetin may, like NaF, also inhibit type I photooxidations, which contribute to hemolysis. Quercetin 78-87 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 8463247-1 1993 We have previously shown that the residues Glu4-Leu5-Arg6 (ELR) preceding the first cysteine at the N terminus of the 72-residue form of interleukin-8 (IL-8) are essential for receptor binding and neutrophil activation (Clark-Lewis, I., Schumacher, C., Baggiolini, M., and Moser, B. Cysteine 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 137-150 8490165-3 1993 In this study, we show that platelets activated with either adenosine-5"-diphosphate or epinephrine induce IL-8 secretion by EC. Adenosine Diphosphate 60-84 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 8490165-3 1993 In this study, we show that platelets activated with either adenosine-5"-diphosphate or epinephrine induce IL-8 secretion by EC. Epinephrine 88-99 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 8218944-6 1993 In competition experiments using [125I]-Gro beta-Tyr, unlabelled IL-8 and Gro beta-Tyr generated superposable displacement curves (IC50: 0.69 +/- 0.15 nM and 0.42 +/- 0.11 nM, respectively). beta-tyr 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 8475106-1 1993 Amino acid deletion and mutagenesis experiments have indicated that the sequences Glu-Leu-Arg (ELR) preceding the first cysteine at the N terminus of interleukin 8 (IL-8) is required for receptor binding and neutrophil activation. Glu-Leu-Arg 82-93 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 8475106-1 1993 Amino acid deletion and mutagenesis experiments have indicated that the sequences Glu-Leu-Arg (ELR) preceding the first cysteine at the N terminus of interleukin 8 (IL-8) is required for receptor binding and neutrophil activation. Glu-Leu-Arg 82-93 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 8475106-1 1993 Amino acid deletion and mutagenesis experiments have indicated that the sequences Glu-Leu-Arg (ELR) preceding the first cysteine at the N terminus of interleukin 8 (IL-8) is required for receptor binding and neutrophil activation. Cysteine 120-128 C-X-C motif chemokine ligand 8 Homo sapiens 150-163 8475106-1 1993 Amino acid deletion and mutagenesis experiments have indicated that the sequences Glu-Leu-Arg (ELR) preceding the first cysteine at the N terminus of interleukin 8 (IL-8) is required for receptor binding and neutrophil activation. Cysteine 120-128 C-X-C motif chemokine ligand 8 Homo sapiens 165-169 8494532-6 1993 Both IL8 (class I)- and TNF (class II)-stimulated Cl- efflux exhibited similar sensitivity to inhibition by different types of ion transport inhibitors [ethacrynic acid (EA), amiloride, 4-acetamido-4"-isothiocyanatostilbene-2,2"-disulfonic acid, anthracene-9-carboxylic acid, and 4-4"-diisothiocyanatostilbene-2,2"-disulfonic acid]. Ethacrynic Acid 153-168 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 8494532-6 1993 Both IL8 (class I)- and TNF (class II)-stimulated Cl- efflux exhibited similar sensitivity to inhibition by different types of ion transport inhibitors [ethacrynic acid (EA), amiloride, 4-acetamido-4"-isothiocyanatostilbene-2,2"-disulfonic acid, anthracene-9-carboxylic acid, and 4-4"-diisothiocyanatostilbene-2,2"-disulfonic acid]. Ethacrynic Acid 170-172 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 8494532-6 1993 Both IL8 (class I)- and TNF (class II)-stimulated Cl- efflux exhibited similar sensitivity to inhibition by different types of ion transport inhibitors [ethacrynic acid (EA), amiloride, 4-acetamido-4"-isothiocyanatostilbene-2,2"-disulfonic acid, anthracene-9-carboxylic acid, and 4-4"-diisothiocyanatostilbene-2,2"-disulfonic acid]. Amiloride 175-184 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 8494532-6 1993 Both IL8 (class I)- and TNF (class II)-stimulated Cl- efflux exhibited similar sensitivity to inhibition by different types of ion transport inhibitors [ethacrynic acid (EA), amiloride, 4-acetamido-4"-isothiocyanatostilbene-2,2"-disulfonic acid, anthracene-9-carboxylic acid, and 4-4"-diisothiocyanatostilbene-2,2"-disulfonic acid]. 4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic Acid 186-244 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 8494532-6 1993 Both IL8 (class I)- and TNF (class II)-stimulated Cl- efflux exhibited similar sensitivity to inhibition by different types of ion transport inhibitors [ethacrynic acid (EA), amiloride, 4-acetamido-4"-isothiocyanatostilbene-2,2"-disulfonic acid, anthracene-9-carboxylic acid, and 4-4"-diisothiocyanatostilbene-2,2"-disulfonic acid]. 9-anthroic acid 246-274 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 8494532-6 1993 Both IL8 (class I)- and TNF (class II)-stimulated Cl- efflux exhibited similar sensitivity to inhibition by different types of ion transport inhibitors [ethacrynic acid (EA), amiloride, 4-acetamido-4"-isothiocyanatostilbene-2,2"-disulfonic acid, anthracene-9-carboxylic acid, and 4-4"-diisothiocyanatostilbene-2,2"-disulfonic acid]. 4-4"-diisothiocyanatostilbene-2,2"-disulfonic acid 280-330 C-X-C motif chemokine ligand 8 Homo sapiens 5-8 8386224-2 1993 Addition of NaF to intact cells resulted in an increase in the release of inositol phosphates (450% of control values; EC50 of approximately 8 mM). Inositol Phosphates 74-93 C-X-C motif chemokine ligand 8 Homo sapiens 12-15 8386224-3 1993 Inclusion of U-73122, an aminosteroid inhibitor of guanine nucleotide-regulated PIC activity in these cells, resulted in a dose-dependent inhibition of NaF-stimulated inositol lipid hydrolysis (IC50 of approximately 3.5 microM). 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 8386224-3 1993 Inclusion of U-73122, an aminosteroid inhibitor of guanine nucleotide-regulated PIC activity in these cells, resulted in a dose-dependent inhibition of NaF-stimulated inositol lipid hydrolysis (IC50 of approximately 3.5 microM). Guanine Nucleotides 51-69 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 8386224-3 1993 Inclusion of U-73122, an aminosteroid inhibitor of guanine nucleotide-regulated PIC activity in these cells, resulted in a dose-dependent inhibition of NaF-stimulated inositol lipid hydrolysis (IC50 of approximately 3.5 microM). inositol lipid 167-181 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 8386224-4 1993 When added to digitonin-permeabilized cells, NaF or guanosine-5"-O-thiotriphosphate (GTP gamma S) resulted in a three- and sevenfold enhancement, respectively, of inositol phosphate release. Digitonin 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 8386224-4 1993 When added to digitonin-permeabilized cells, NaF or guanosine-5"-O-thiotriphosphate (GTP gamma S) resulted in a three- and sevenfold enhancement, respectively, of inositol phosphate release. Guanosine 5'-O-(3-Thiotriphosphate) 85-96 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 8386224-4 1993 When added to digitonin-permeabilized cells, NaF or guanosine-5"-O-thiotriphosphate (GTP gamma S) resulted in a three- and sevenfold enhancement, respectively, of inositol phosphate release. Inositol Phosphates 163-181 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 8386224-5 1993 In the combined presence of optimal concentrations of NaF and GTP gamma S, inositol phosphate release was less than additive, indicative of a common site of action. Inositol Phosphates 75-93 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 8386224-6 1993 Inclusion of 2-5 mM concentrations of guanosine-5"-O-(2-thiodiphosphate) (GDP beta S) fully blocked phosphoinositide hydrolysis elicited by GTP gamma S, whereas that induced by NaF was partially inhibited (65%). guanosine 5'-O-(2-thiodiphosphate) 74-84 C-X-C motif chemokine ligand 8 Homo sapiens 177-180 8386224-6 1993 Inclusion of 2-5 mM concentrations of guanosine-5"-O-(2-thiodiphosphate) (GDP beta S) fully blocked phosphoinositide hydrolysis elicited by GTP gamma S, whereas that induced by NaF was partially inhibited (65%). Sulfur 83-84 C-X-C motif chemokine ligand 8 Homo sapiens 177-180 8386224-7 1993 However, preincubation of the cells with GDP beta S resulted in a greater reduction in the ability of NaF to stimulate inositol phosphate release (87% inhibition). guanosine 5'-O-(2-thiodiphosphate) 41-51 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 8386224-7 1993 However, preincubation of the cells with GDP beta S resulted in a greater reduction in the ability of NaF to stimulate inositol phosphate release (87% inhibition). Inositol Phosphates 119-137 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 8386224-8 1993 Both GTP gamma S and NaF-stimulated inositol phosphate release were inhibited by inclusion of 10 microM U-73122 (54-71%). Inositol Phosphates 36-54 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 8386224-8 1993 Both GTP gamma S and NaF-stimulated inositol phosphate release were inhibited by inclusion of 10 microM U-73122 (54-71%). 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 104-111 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 8386224-10 1993 These results indicate that in SK-N-SH cells, little evidence exists for direct stimulation of PIC by NaF and that the majority of inositol phosphate release that occurs in the presence of NaF can be attributed to activation of Gp. Inositol Phosphates 131-149 C-X-C motif chemokine ligand 8 Homo sapiens 189-192 8385495-1 1993 Sodium fluoride (NaF) alone below the concentration of 10 mM had no effect on platelet intracellular Ca2+ ([Ca2+]i). Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 8385495-4 1993 NaF was also effective in inhibiting thrombin- or U-46619-induced Mn2+ entry. Manganese(2+) 66-70 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8385495-5 1993 This inhibitory effect of NaF on Ca2+ influx occurred after a lag of at least 30 s. However, Ca2+ influx induced by ionomycin-induced Ca2+ depletion or by thapsigargin, a Ca(2+)-ATPase inhibitor, was only partially suppressed by NaF treatment. Ionomycin 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 8385495-5 1993 This inhibitory effect of NaF on Ca2+ influx occurred after a lag of at least 30 s. However, Ca2+ influx induced by ionomycin-induced Ca2+ depletion or by thapsigargin, a Ca(2+)-ATPase inhibitor, was only partially suppressed by NaF treatment. Ionomycin 116-125 C-X-C motif chemokine ligand 8 Homo sapiens 229-232 8385495-5 1993 This inhibitory effect of NaF on Ca2+ influx occurred after a lag of at least 30 s. However, Ca2+ influx induced by ionomycin-induced Ca2+ depletion or by thapsigargin, a Ca(2+)-ATPase inhibitor, was only partially suppressed by NaF treatment. Thapsigargin 155-167 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 8463247-1 1993 We have previously shown that the residues Glu4-Leu5-Arg6 (ELR) preceding the first cysteine at the N terminus of the 72-residue form of interleukin-8 (IL-8) are essential for receptor binding and neutrophil activation (Clark-Lewis, I., Schumacher, C., Baggiolini, M., and Moser, B. Cysteine 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 152-156 8463247-7 1993 The most potent were IL-8(6-72), with Arg6 at the N terminus, and IL-8,AAR(7-72) with N-terminal Ala4-Ala5 instead of Glu4-Leu5. ala4-ala5 97-106 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 8104581-10 1993 NaF-treated plasma gave a significant underestimation of 3OHB. 3ohb 57-61 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8344717-8 1993 The optimal concentration in the chemotactic activity of CT/IL-8, equivalent to that of bacterial chemotactic peptide fMet-Leu-Phe (10 nM), was found to be 5 nM. Leucine 123-126 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 8344717-8 1993 The optimal concentration in the chemotactic activity of CT/IL-8, equivalent to that of bacterial chemotactic peptide fMet-Leu-Phe (10 nM), was found to be 5 nM. Phenylalanine 127-130 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 8458381-0 1993 Human peripheral blood eosinophils produce and release interleukin-8 on stimulation with calcium ionophore. Calcium 89-96 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 8458381-2 1993 Following in vitro culture of 99% pure eosinophils with calcium ionophore, released IL-8 was detectable by enzyme-linked immunosorbent assay in supernatants. Calcium 56-63 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 8458381-4 1993 Furthermore, eosinophil production of IL-8 in the presence of calcium ionophore could be inhibited with the immunomodulating agent cyclosporin A and the protein synthesis inhibitor cycloheximide. Calcium 62-69 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8458381-4 1993 Furthermore, eosinophil production of IL-8 in the presence of calcium ionophore could be inhibited with the immunomodulating agent cyclosporin A and the protein synthesis inhibitor cycloheximide. Cyclosporine 131-144 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8458381-4 1993 Furthermore, eosinophil production of IL-8 in the presence of calcium ionophore could be inhibited with the immunomodulating agent cyclosporin A and the protein synthesis inhibitor cycloheximide. Cycloheximide 181-194 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8458381-5 1993 In addition, following stimulation of highly purified blood eosinophils with calcium ionophore, IL-8 mRNA was detectable after polymerase chain reaction amplification. Calcium 77-84 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 8458381-6 1993 In comparison with other cells on stimulation with calcium ionophore, eosinophils produce about half as much IL-8 as neutrophils but significantly more than purified T cells. Calcium 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 8458381-8 1993 Finally, following calcium ionophore stimulation blood eosinophils were shown to contain cytoplasmic IL-8 by employing a monoclonal antibody against IL-8 in conjunction with immunohistochemistry. Calcium 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 8458381-8 1993 Finally, following calcium ionophore stimulation blood eosinophils were shown to contain cytoplasmic IL-8 by employing a monoclonal antibody against IL-8 in conjunction with immunohistochemistry. Calcium 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 8464050-1 1993 The backbone dynamics of the cytokine interleukin-8, a symmetric homodimer of overall molecular mass 16 kDa, has been investigated at pH 5.2 by means of 15N relaxation measurements using heteronuclear two-dimensional inverse detected 1H-15N spectroscopy. 15n 153-156 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 7681085-4 1993 Calcitriol was used to induce a high level of CD14 expression in the human monocyte-like cell line THP-1, resulting in enhanced responses of these cells to LPS-LBP complexes manifested by enhanced binding of LPS and a decrease in the amount of LPS needed to induce IL-8 release. Calcitriol 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 265-269 8454590-6 1993 Incubation of neutrophils with sulfhydryl group-modifying reagents, N-ethylmaleimide and diazene dicarboxylic acid bis-N,N-dimethylamide (diamide), severely impaired the binding of 125I-IL-8 to neutrophils. Ethylmaleimide 68-84 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 8454590-6 1993 Incubation of neutrophils with sulfhydryl group-modifying reagents, N-ethylmaleimide and diazene dicarboxylic acid bis-N,N-dimethylamide (diamide), severely impaired the binding of 125I-IL-8 to neutrophils. Diamide 89-136 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 8454590-7 1993 Treatment with 0.8 mM N-ethylmaleimide and 0.4 mM diamide inhibit binding of 125I-IL-8 to the neutrophils by 62 and 60%, respectively. Ethylmaleimide 22-38 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 8454590-7 1993 Treatment with 0.8 mM N-ethylmaleimide and 0.4 mM diamide inhibit binding of 125I-IL-8 to the neutrophils by 62 and 60%, respectively. Diamide 50-57 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 8454590-11 1993 At a concentration of 0.4 mM, N-ethylmaleimide reduced the IL-8-induced (10 micrograms/ml) release of myeloperoxidase by 50%. Ethylmaleimide 30-46 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 8454590-13 1993 Finally, N-ethylmaleimide severely affected the overall binding and total uptake of 125I-IL-8 to the neutrophils at 37 degrees C, a condition required for receptor-mediated internalization of the ligand and recycling of the receptor to the surface of neutrophils. Ethylmaleimide 9-25 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 8464050-1 1993 The backbone dynamics of the cytokine interleukin-8, a symmetric homodimer of overall molecular mass 16 kDa, has been investigated at pH 5.2 by means of 15N relaxation measurements using heteronuclear two-dimensional inverse detected 1H-15N spectroscopy. Hydrogen 234-236 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 7680648-5 1993 Preincubation of the cells with cycloheximide "superinduced" the level of IL-8 mRNA stimulated by TNF alpha and IL-1 beta and RANTES mRNA stimulated by IL-1 beta, but decreased the expression of RANTES mRNA in response to TNF alpha. Cycloheximide 32-45 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 8464050-1 1993 The backbone dynamics of the cytokine interleukin-8, a symmetric homodimer of overall molecular mass 16 kDa, has been investigated at pH 5.2 by means of 15N relaxation measurements using heteronuclear two-dimensional inverse detected 1H-15N spectroscopy. 15n 237-240 C-X-C motif chemokine ligand 8 Homo sapiens 38-51 8381770-8 1993 Inhibitory effects were obtained when GTP-binding protein functions were stimulated with sodium fluoride (NaF). Sodium Fluoride 89-104 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 8384238-4 1993 IFN-gamma also induced priming toward the stimulant NaF, a direct activator of guanine nucleotide regulatory proteins. Guanine Nucleotides 79-97 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 8382247-2 1993 NaF and FMLP stimulated superoxide release from both groups of cells, but the response was attenuated in RA-differentiated cells. Superoxides 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 8382840-6 1993 Using three different techniques--the E. coli killing assay (8 patients), the production of reactive oxygen as determined by cytochrome c reduction (7 patients) and chemiluminescence (8 patients)--a significant stimulation of neutrophil function at a concentration of 10 nm IL-8 was found in all test systems. reactive oxygen 92-107 C-X-C motif chemokine ligand 8 Homo sapiens 274-278 8384226-6 1993 RESULTS: Nedocromil sodium inhibited the chemotactic response toward FMLP and NAF/IL-8 of GM-CSF primed eosinophils approximately 60% (inhibitory concentration of 50% [IC50] approximately 1 to 10 nmol/L), whereas these responses of IL-3 primed eosinophils was completely inhibited (IC50 approximately 1 nmol/L). Nedocromil 9-26 C-X-C motif chemokine ligand 8 Homo sapiens 78-81 8384226-6 1993 RESULTS: Nedocromil sodium inhibited the chemotactic response toward FMLP and NAF/IL-8 of GM-CSF primed eosinophils approximately 60% (inhibitory concentration of 50% [IC50] approximately 1 to 10 nmol/L), whereas these responses of IL-3 primed eosinophils was completely inhibited (IC50 approximately 1 nmol/L). Nedocromil 9-26 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 7679201-1 1993 Conflicting evidence has been reported concerning the mutagenicity of sodium fluoride (NaF), especially clastogenicity at concentrations of more than 1 mM. Sodium Fluoride 70-85 C-X-C motif chemokine ligand 8 Homo sapiens 87-90 8382084-5 1993 Additionally, NaF and A23187 completely abrogated adenosine inhibition of fMLP-stimulated neutrophil adherence. Adenosine 50-59 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 8381837-4 1993 Bacterial toxins such as cholera toxin or pertussis toxin inhibited IL-8-induced chemokinetic activity, suggesting the involvement of guanine nucleotide-binding (G) proteins in IL-8 signal transduction in these cells. Guanine Nucleotides 134-152 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 8381837-4 1993 Bacterial toxins such as cholera toxin or pertussis toxin inhibited IL-8-induced chemokinetic activity, suggesting the involvement of guanine nucleotide-binding (G) proteins in IL-8 signal transduction in these cells. Guanine Nucleotides 134-152 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 8381837-9 1993 Various concentrations of IL-8 enhanced the binding of GTP-gamma 35 S to IANK cell membranes, which further indicates the coupling of G proteins to IL-8 receptors in IANK cells. Guanosine Triphosphate 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 8381837-9 1993 Various concentrations of IL-8 enhanced the binding of GTP-gamma 35 S to IANK cell membranes, which further indicates the coupling of G proteins to IL-8 receptors in IANK cells. Guanosine Triphosphate 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 8383457-10 1993 However, NaF and forskolin stimulation of cAMP was markedly decreased in the treated group. Cyclic AMP 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 8441897-5 1993 Significantly higher amounts of alkali soluble fluoride were formed on the enamel from the 2% and 0.2% NaF solutions, as compared with the control. Fluorides 47-55 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 8432783-6 1993 Cotreatment of chorion cells or decidual cells with IL-1 beta and actinomycin D or cycloheximide abrogated IL-8 production. Dactinomycin 66-79 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 8432783-6 1993 Cotreatment of chorion cells or decidual cells with IL-1 beta and actinomycin D or cycloheximide abrogated IL-8 production. Cycloheximide 83-96 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 8431115-4 1993 Steroids greatly reduced the clinical response to endotoxin and attenuated the appearance of tumor necrosis factor, IL-6, and IL-8 in the circulation. Steroids 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 8473010-7 1993 Further observations revealed that, in human PMN, degradation of IL-8 mRNA is finely regulated, and that cycloheximide (CHX), an inhibitor of protein synthesis, super-induces the mRNA accumulation for IL-8 in a dose- and time-dependent manner. Cycloheximide 105-118 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 8473010-7 1993 Further observations revealed that, in human PMN, degradation of IL-8 mRNA is finely regulated, and that cycloheximide (CHX), an inhibitor of protein synthesis, super-induces the mRNA accumulation for IL-8 in a dose- and time-dependent manner. Cycloheximide 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 8473010-7 1993 Further observations revealed that, in human PMN, degradation of IL-8 mRNA is finely regulated, and that cycloheximide (CHX), an inhibitor of protein synthesis, super-induces the mRNA accumulation for IL-8 in a dose- and time-dependent manner. Cycloheximide 120-123 C-X-C motif chemokine ligand 8 Homo sapiens 201-205 8441897-6 1993 There was also a significant increase in the firmly bound fluoride after treatment with the neutral 2% NaF solution. Fluorides 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 8418897-6 1993 Enzyme activity was markedly inhibited by NaF, not influenced by excess glycerophosphate and slightly attenuated by propranolol, an inhibitor of PA phosphohydrolase in other systems. Propranolol 116-127 C-X-C motif chemokine ligand 8 Homo sapiens 42-45 8381283-0 1993 Studies on the regulatory mechanisms of interleukin-8 gene expression in resting and IFN-gamma-treated neutrophils: evidence on the capability of staurosporine of inducing the production of interleukin-8 by human neutrophils. Staurosporine 146-159 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 8381283-0 1993 Studies on the regulatory mechanisms of interleukin-8 gene expression in resting and IFN-gamma-treated neutrophils: evidence on the capability of staurosporine of inducing the production of interleukin-8 by human neutrophils. Staurosporine 146-159 C-X-C motif chemokine ligand 8 Homo sapiens 190-203 7524285-0 1993 L-arginine/nitric oxide pathway: a possible signal transduction mechanism for the regulation of the chemokine IL-8 in human mesangial cells. Arginine 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 7524285-0 1993 L-arginine/nitric oxide pathway: a possible signal transduction mechanism for the regulation of the chemokine IL-8 in human mesangial cells. Nitric Oxide 11-23 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 8380724-0 1993 Interleukin-8-stimulated polyphosphoinositide hydrolysis in human peripheral blood lymphocytes. Phosphatidylinositol Phosphates 25-45 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 8380724-1 1993 We have attempted to provide evidence for the production of inositol phosphate (IP) metabolites as an indication of specific receptor-mediated signal transduction in human peripheral blood lymphocytes (PBL) in response to interleukin-8 (IL-8). Inositol Phosphates 60-78 C-X-C motif chemokine ligand 8 Homo sapiens 222-235 8380724-1 1993 We have attempted to provide evidence for the production of inositol phosphate (IP) metabolites as an indication of specific receptor-mediated signal transduction in human peripheral blood lymphocytes (PBL) in response to interleukin-8 (IL-8). Inositol Phosphates 60-78 C-X-C motif chemokine ligand 8 Homo sapiens 237-241 8380724-1 1993 We have attempted to provide evidence for the production of inositol phosphate (IP) metabolites as an indication of specific receptor-mediated signal transduction in human peripheral blood lymphocytes (PBL) in response to interleukin-8 (IL-8). Inositol Phosphates 80-82 C-X-C motif chemokine ligand 8 Homo sapiens 222-235 8380724-1 1993 We have attempted to provide evidence for the production of inositol phosphate (IP) metabolites as an indication of specific receptor-mediated signal transduction in human peripheral blood lymphocytes (PBL) in response to interleukin-8 (IL-8). Inositol Phosphates 80-82 C-X-C motif chemokine ligand 8 Homo sapiens 237-241 8380724-4 1993 Compared with phytohemagglutinin (PHA), which stimulated an increase in IP metabolites and, specifically, IP3 by greater than threefold, human recombinant (hr) IL-8 (1 nmol/L) also stimulated an increase in IP metabolites, as measured by HPLC, and a greater than threefold increase in IP3. Inositol 1,4,5-Trisphosphate 285-288 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 7901957-15 1993 We showed that mRNA for IL-8 could be expressed in highly purified T lymphocytes only upon stimulation with ionomycin and PHA or PMA and PHA, and to a lesser extent PMA and IL-2. Ionomycin 108-117 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 8273591-1 1993 Several protein kinase inhibitors (PKIs) were investigated for their effects on IL-1 beta, TNF alpha and PMA-induced IL-8 production from human umbilical vein endothelial cells (HUVEC). Tetradecanoylphorbol Acetate 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 7908198-4 1993 It was of interest to note that serum IL-8 levels were increased transiently after abstinence from alcohol in patients with alcoholic hepatitis. Alcohols 99-106 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8273591-3 1993 Staurosporine, a potent but non-specific inhibitor of protein kinases, inhibited PMA-induced (IC50 2 nM) but not IL-1 beta or TNF alpha (IC50 > 200 nM) induced IL-8 production. Staurosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 8443122-1 1993 Few known genes (IL-2, members of the IL-8 family, interferon-gamma) are induced in T cells only through the combined effect of phorbol myristic acetate (PMA) and a Ca(2+)-ionophore, and expression of only these genes can be fully suppressed by Cyclosporin A (CyA). phorbol myristic acetate 128-152 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8273591-5 1993 However, the macrolide protein kinase inhibitor geldanamycin (IC50 = 30 nM), but not the closely related analog herbimycin A (5-500 nM), inhibited IL-8 production by 60%. geldanamycin 48-60 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 8273591-6 1993 Northern blot analysis of IL-8 mRNA revealed that staurosporine suppressed mRNA increase following stimulation by PMA but not by IL-1. Staurosporine 50-63 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 8420495-11 1993 CONCLUSION: Based on these results, we speculate that, although IL-8 may exert a synergistic effect with C5a/C5a des Arg in the induction of transepidermal leukocyte chemotaxis, it constitutes a proinflammatory cytokine that is involved in the production of the persistent inflammatory changes characterized by a T-lymphocyte infiltration. Arginine 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 8457524-1 1993 In the present study the effect of replacement of dietary fat by palm oil in the normal Western diet on the in vitro release of the inflammatory cytokines tumour necrosis factor (TNF), interleukin (IL)-6 and IL-8 was examined. Palm Oil 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 7506142-8 1993 The release of tumour necrosis factor-alpha (TNF-alpha) initiates the release of interleukin-1 and interleukin-8, which in turn liberate cyclo-oxygenase metabolites and sympathomimetic amines, respectively. Amines 185-191 C-X-C motif chemokine ligand 8 Homo sapiens 99-112 7514580-0 1993 Effect of tenoxicam and indomethacin on the chemotaxis induced by substance P and interleukin-8 on human monocytes and polymorphonuclear cells. tenoxicam 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 7514580-0 1993 Effect of tenoxicam and indomethacin on the chemotaxis induced by substance P and interleukin-8 on human monocytes and polymorphonuclear cells. Indomethacin 24-36 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 8420406-9 1993 TNF, IL-6, and IL-8 in BAL fluid supernatant concentrations increased in a time and exposure-dependent fashion after zinc oxide welding fume exposure. Zinc Oxide 117-127 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 8402812-6 1993 While the numerical difference in efficacy between NaF and SMFP measured between 5 and 10% (total DMFS) over a 2- to 3-year clinical period, this could be expected, on theoretical grounds, to propagate to substantially larger differences (e.g. 10-20%) over 10-20 years. dmfs 98-102 C-X-C motif chemokine ligand 8 Homo sapiens 51-54 7514580-3 1993 We investigated in vitro the effect of two non-steroidal antiinflammatory drugs, tenoxicam and indomethacin, on the chemotactic effect of substance P and interleukin-8 at concentrations that can be reached in the synovial fluid of arthritic patients. tenoxicam 81-90 C-X-C motif chemokine ligand 8 Homo sapiens 154-167 8443122-1 1993 Few known genes (IL-2, members of the IL-8 family, interferon-gamma) are induced in T cells only through the combined effect of phorbol myristic acetate (PMA) and a Ca(2+)-ionophore, and expression of only these genes can be fully suppressed by Cyclosporin A (CyA). Tetradecanoylphorbol Acetate 154-157 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 7514580-3 1993 We investigated in vitro the effect of two non-steroidal antiinflammatory drugs, tenoxicam and indomethacin, on the chemotactic effect of substance P and interleukin-8 at concentrations that can be reached in the synovial fluid of arthritic patients. Indomethacin 95-107 C-X-C motif chemokine ligand 8 Homo sapiens 154-167 8443122-1 1993 Few known genes (IL-2, members of the IL-8 family, interferon-gamma) are induced in T cells only through the combined effect of phorbol myristic acetate (PMA) and a Ca(2+)-ionophore, and expression of only these genes can be fully suppressed by Cyclosporin A (CyA). Cyclosporine 245-258 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8443122-1 1993 Few known genes (IL-2, members of the IL-8 family, interferon-gamma) are induced in T cells only through the combined effect of phorbol myristic acetate (PMA) and a Ca(2+)-ionophore, and expression of only these genes can be fully suppressed by Cyclosporin A (CyA). Cyclosporine 260-263 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 8429521-6 1993 However, IL-8 production by neonatal CBMCs was down-regulated by dexamethasone, a glucocorticoid which is clinically administered to mothers to promote fetal lung maturity in preterm delivery. cbmcs 37-42 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 8427047-1 1993 The anabolic effects of sodium fluoride (NaF) on trabecular bone mass in osteoporosis is now well established. Sodium Fluoride 24-39 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 8429521-6 1993 However, IL-8 production by neonatal CBMCs was down-regulated by dexamethasone, a glucocorticoid which is clinically administered to mothers to promote fetal lung maturity in preterm delivery. Dexamethasone 65-78 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 8461565-1 1993 The future of sodium fluoride (NaF), the most potent osteoblast stimulator known to man, is in the balance. Sodium Fluoride 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 18475524-0 1993 The effect of inhibition of leukotriene synthesis on the activity of interleukin-8 and granulocyte-macrophage colony-stimulating factor. Leukotrienes 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 69-82 18475524-1 1993 The cytokines interleukin-8 (IL-8) and granulocyte-macrophage colony-stimulating factor (GM-CSF) enhanced the extracellular release of arachidonate metabolites from ionophore-stimulated neutrophils by 145 +/- 10% (mean +/- S.E.M., n = 13) and 182 +/- 11% (n = 16), respectively. Arachidonic Acid 135-147 C-X-C motif chemokine ligand 8 Homo sapiens 14-27 18475524-1 1993 The cytokines interleukin-8 (IL-8) and granulocyte-macrophage colony-stimulating factor (GM-CSF) enhanced the extracellular release of arachidonate metabolites from ionophore-stimulated neutrophils by 145 +/- 10% (mean +/- S.E.M., n = 13) and 182 +/- 11% (n = 16), respectively. Arachidonic Acid 135-147 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 18475524-3 1993 Neither inhibitor affected the upregulation of CD11b beta(2)-integrin expression or priming of superoxide generation stimulated by IL-8 and GM-CSF. Superoxides 95-105 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 8216828-3 1993 Our findings demonstrate that PBMC adherent to either plastic or physiological surfaces in combination with an inflammatory agonist is both a potent and efficacious signal for the expression and production of the neutrophil chemotactic/activating cytokine, IL-8. PBMC 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 257-261 8380937-1 1993 Whereas we observed previously that concentrations of the lipoxygenase inhibitor nordihydroguaiaretic acid that inhibited leukotriene B4 release from lipopolysaccharide-stimulated human alveolar macrophages in vitro also inhibited subsequent interleukin-8 release, we hypothesized that leukotriene B4 release was required for the release of interleukin-8. Masoprocol 81-106 C-X-C motif chemokine ligand 8 Homo sapiens 242-255 21043600-3 1993 Phorbol myristate acetate (PMA; a PKC activator), sodium fluoride (NaF; a putative G protein activator), ADP and collagen stimulated the uptake of [(45)Ca(2+)] by platelets in dose-dependent manners. Sodium Fluoride 50-65 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 21043600-5 1993 PMA-stimulated and NaF-stimulated [(45)Ca(2+)] uptake was inhibited in concentration-dependent manners by the PKC inhibitor, staurosporine. Staurosporine 125-138 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 8380937-0 1993 The effect of inhibition of leukotriene B4 release on lipopolysaccharide-induced production of neutrophil attractant/activation protein-1 (interleukin-8) by human alveolar macrophages. Leukotriene B4 28-42 C-X-C motif chemokine ligand 8 Homo sapiens 139-152 8380937-1 1993 Whereas we observed previously that concentrations of the lipoxygenase inhibitor nordihydroguaiaretic acid that inhibited leukotriene B4 release from lipopolysaccharide-stimulated human alveolar macrophages in vitro also inhibited subsequent interleukin-8 release, we hypothesized that leukotriene B4 release was required for the release of interleukin-8. Masoprocol 81-106 C-X-C motif chemokine ligand 8 Homo sapiens 341-354 1334090-13 1992 The enzyme was inhibited by sphingosine and chloropromazine, and less potently, by propranolol and NaF. Sphingosine 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 8256463-5 1993 Fluorescent light intensity is, however, significantly increased, indicating an increased transcapillary diffusion of sodium fluorescein (NaF) as a marker for enhanced leakage of the capillaries in the early stage of the disease. Fluorescein 118-136 C-X-C motif chemokine ligand 8 Homo sapiens 138-141 1334781-7 1992 IL-8 had apparent BCA, which was not so high as that of C5a. alpha-bromocinnamaldehyde 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1281554-5 1992 An IL-8 antisense oligonucleotide specifically blocked the production of monocyte-induced angiogenic activity. Oligonucleotides 18-33 C-X-C motif chemokine ligand 8 Homo sapiens 3-7 1332845-2 1992 Pretreatment of pituitary cell cultures with NaF (a guanyl nucleotide binding protein activator, 10 mM, 3 h) also decreased subsequent GnRH-stimulated LH release, and in addition, provoked a decrease in GnRH receptor number, an increase in GnRH receptor affinity, reduction of GnRH-stimulated IP production to basal levels, and an increase in the amount of LH released in response to stimulation with the calcium ionophore A23187. Luteinizing Hormone 151-153 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 1281615-4 1992 Repeat fluorescein angiograms 6 weeks after placing angiogenic doses of rIL-8 demonstrated significant regression (P = 0.01) of the vascularity present at 2 weeks, suggesting that IL-8 angiogenesis undergoes dynamic modulation similar to that normally seen in wound healing. Fluorescein 7-18 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 1332845-2 1992 Pretreatment of pituitary cell cultures with NaF (a guanyl nucleotide binding protein activator, 10 mM, 3 h) also decreased subsequent GnRH-stimulated LH release, and in addition, provoked a decrease in GnRH receptor number, an increase in GnRH receptor affinity, reduction of GnRH-stimulated IP production to basal levels, and an increase in the amount of LH released in response to stimulation with the calcium ionophore A23187. Luteinizing Hormone 357-359 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 1332845-2 1992 Pretreatment of pituitary cell cultures with NaF (a guanyl nucleotide binding protein activator, 10 mM, 3 h) also decreased subsequent GnRH-stimulated LH release, and in addition, provoked a decrease in GnRH receptor number, an increase in GnRH receptor affinity, reduction of GnRH-stimulated IP production to basal levels, and an increase in the amount of LH released in response to stimulation with the calcium ionophore A23187. Calcium 405-412 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 1332845-2 1992 Pretreatment of pituitary cell cultures with NaF (a guanyl nucleotide binding protein activator, 10 mM, 3 h) also decreased subsequent GnRH-stimulated LH release, and in addition, provoked a decrease in GnRH receptor number, an increase in GnRH receptor affinity, reduction of GnRH-stimulated IP production to basal levels, and an increase in the amount of LH released in response to stimulation with the calcium ionophore A23187. Calcimycin 423-429 C-X-C motif chemokine ligand 8 Homo sapiens 45-48 1332845-6 1992 GnRH-stimulated LH release was inhibited immediately after NaF pretreatment (1 microM GnRH-stimulated LH release in NaF-pretreated cells was 65% of control levels). Luteinizing Hormone 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 1332845-6 1992 GnRH-stimulated LH release was inhibited immediately after NaF pretreatment (1 microM GnRH-stimulated LH release in NaF-pretreated cells was 65% of control levels). Luteinizing Hormone 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 1332845-6 1992 GnRH-stimulated LH release was inhibited immediately after NaF pretreatment (1 microM GnRH-stimulated LH release in NaF-pretreated cells was 65% of control levels). Luteinizing Hormone 102-104 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 1332845-6 1992 GnRH-stimulated LH release was inhibited immediately after NaF pretreatment (1 microM GnRH-stimulated LH release in NaF-pretreated cells was 65% of control levels). Luteinizing Hormone 102-104 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 1332845-8 1992 A23187-provoked LH release was enhanced immediately after NaF pretreatment (30 microM A23187-stimulated LH release in NaF-pretreated cells was 170% of control levels). Calcimycin 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 1332845-8 1992 A23187-provoked LH release was enhanced immediately after NaF pretreatment (30 microM A23187-stimulated LH release in NaF-pretreated cells was 170% of control levels). Calcimycin 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 1332845-8 1992 A23187-provoked LH release was enhanced immediately after NaF pretreatment (30 microM A23187-stimulated LH release in NaF-pretreated cells was 170% of control levels). Luteinizing Hormone 16-18 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 1332845-8 1992 A23187-provoked LH release was enhanced immediately after NaF pretreatment (30 microM A23187-stimulated LH release in NaF-pretreated cells was 170% of control levels). Calcimycin 86-92 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 1332845-8 1992 A23187-provoked LH release was enhanced immediately after NaF pretreatment (30 microM A23187-stimulated LH release in NaF-pretreated cells was 170% of control levels). Calcimycin 86-92 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 1332845-8 1992 A23187-provoked LH release was enhanced immediately after NaF pretreatment (30 microM A23187-stimulated LH release in NaF-pretreated cells was 170% of control levels). Luteinizing Hormone 104-106 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 1332845-8 1992 A23187-provoked LH release was enhanced immediately after NaF pretreatment (30 microM A23187-stimulated LH release in NaF-pretreated cells was 170% of control levels). Luteinizing Hormone 104-106 C-X-C motif chemokine ligand 8 Homo sapiens 118-121 1332845-10 1992 Furthermore, both NaF and GnRH pretreatment still provoked a decrease in gonadotrope responsiveness when IP production was inhibited by the phospholipase C inhibitor U-73122. 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 166-173 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1292643-3 1992 Levels of IL-8 were significantly correlated with the influx of neutrophils, plasma protein extravasation and with the PaO2/FiO2 ratio. pao2 119-123 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 1292643-3 1992 Levels of IL-8 were significantly correlated with the influx of neutrophils, plasma protein extravasation and with the PaO2/FiO2 ratio. fio2 124-128 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 1331181-4 1992 DMSO was found to directly inhibit IL-8 expression at the level of transcription. Dimethyl Sulfoxide 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 1331181-5 1992 Furthermore, this effect was not LPS-specific, in that IL-8 production was reduced by DMSO to a similar extent upon stimulation of blood with phytohemagglutinin, aggregated immune complexes, TNF, or IL-1 beta. Dimethyl Sulfoxide 86-90 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 1331181-6 1992 Other oxygen radical scavengers that have been shown to inhibit OH.-dependent reactions (dimethyl thiourea, thiourea, mannitol, and ethanol) also inhibited IL-8 production. Reactive Oxygen Species 6-20 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 1331181-0 1992 Oxygen radical scavengers selectively inhibit interleukin 8 production in human whole blood. Reactive Oxygen Species 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 46-59 1331181-6 1992 Other oxygen radical scavengers that have been shown to inhibit OH.-dependent reactions (dimethyl thiourea, thiourea, mannitol, and ethanol) also inhibited IL-8 production. 1,3-dimethylthiourea 89-106 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 1331181-2 1992 scavenger dimethyl sulfoxide (DMSO) was found to dose-dependently inhibit interleukin 8 (IL-8) production in LPS-stimulated human whole blood. Dimethyl Sulfoxide 10-28 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 1331181-2 1992 scavenger dimethyl sulfoxide (DMSO) was found to dose-dependently inhibit interleukin 8 (IL-8) production in LPS-stimulated human whole blood. Dimethyl Sulfoxide 10-28 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 1331181-6 1992 Other oxygen radical scavengers that have been shown to inhibit OH.-dependent reactions (dimethyl thiourea, thiourea, mannitol, and ethanol) also inhibited IL-8 production. Thiourea 98-106 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 1331181-2 1992 scavenger dimethyl sulfoxide (DMSO) was found to dose-dependently inhibit interleukin 8 (IL-8) production in LPS-stimulated human whole blood. Dimethyl Sulfoxide 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 74-87 1331181-2 1992 scavenger dimethyl sulfoxide (DMSO) was found to dose-dependently inhibit interleukin 8 (IL-8) production in LPS-stimulated human whole blood. Dimethyl Sulfoxide 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 1331181-6 1992 Other oxygen radical scavengers that have been shown to inhibit OH.-dependent reactions (dimethyl thiourea, thiourea, mannitol, and ethanol) also inhibited IL-8 production. Mannitol 118-126 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 1331181-3 1992 At a concentration of 1% (vol/vol), DMSO blocked IL-8 release by approximately 90% in the presence of 1 microgram/ml LPS at a 24-h time point, but did not affect cell viability or reduce the production of tumor necrosis factor (TNF), interleukin 6, or interleukin-1 beta (IL-1 beta). Dimethyl Sulfoxide 36-40 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 1331181-6 1992 Other oxygen radical scavengers that have been shown to inhibit OH.-dependent reactions (dimethyl thiourea, thiourea, mannitol, and ethanol) also inhibited IL-8 production. Ethanol 132-139 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 1331181-7 1992 Conversely, addition of H2O2 caused a dose-dependent stimulation of IL-8 release. Hydrogen Peroxide 24-28 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 1331181-8 1992 These results provide evidence that reactive oxygen metabolites play an important role in the regulation of IL-8 production and suggest that reduction of IL-8 release may contribute to the beneficial effects of antioxidants in experimental models of inflammation and ischemia/reperfusion injury. Oxygen 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 1382479-0 1992 Interleukin-8 and RANTES inhibit basophil histamine release induced with monocyte chemotactic and activating factor/monocyte chemoattractant peptide-1 and histamine releasing factor. Histamine 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1383321-3 1992 After pretreatment with IL-3, significant histamine release was observed with 10(-8) M and 10(-7) M IL-8 and 10(-7) M NAP-2, but not with the other peptides. Histamine 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 1383321-4 1992 At higher concentrations (10(-6) M), however, all IL-8 analogs, as well as the unrelated cationic peptides poly-D-lysine, histone VS, and lysozyme, induced histamine release to variable degrees. Histamine 156-165 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 1383321-8 1992 IL-8 and, to a lesser extent, NAP-2 led to a transient rise of cytosolic free calcium concentration ([Ca2+]i), which was independent of a preexposure to IL-3. Calcium 78-85 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1401924-6 1992 Maximum accumulation of IL-8 mRNA was observed after 6 h of incubation with LR, and the elevation persisted over 24 h. Inhibition of protein synthesis by cycloheximide resulted in superinduction of IL-8 mRNAs by LR. Cycloheximide 154-167 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 1401924-6 1992 Maximum accumulation of IL-8 mRNA was observed after 6 h of incubation with LR, and the elevation persisted over 24 h. Inhibition of protein synthesis by cycloheximide resulted in superinduction of IL-8 mRNAs by LR. Cycloheximide 154-167 C-X-C motif chemokine ligand 8 Homo sapiens 198-202 1401924-9 1992 Gel shift assays with oligonucleotides containing the consensus NF-kappa B binding sequences of the IL-8 and Ig kappa light chain genes showed enhanced binding activity in nuclear extracts from cells incubated with LR. Oligonucleotides 22-38 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 1402020-4 1992 Thus, the increase was due to extra- and intracellular cooperative mobilization of Ca2+, as supported by the reduced effect of IL-8 on [Ca2+]i after quenching with Mn2+. Manganese(2+) 164-168 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 1438244-7 1992 Treatment of membranes with digitonin resulted in the preferential solubilization of a single receptor species, corresponding to p44, that bound GRO alpha and NAP-2 with low affinity (Kd = 30 nM) and IL-8 with high affinity (Kd = 0.4 nM). Digitonin 28-37 C-X-C motif chemokine ligand 8 Homo sapiens 200-204 1438244-8 1992 Exposure of neutrophil membranes to 100 microM guanosine 5"-[gamma-thio]triphosphate led to a 75-fold increase of the Kd in approximately 60% of the IL-8 receptors. Guanosine 5'-O-(3-Thiotriphosphate) 47-84 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 1438244-11 1992 These results demonstrate that human neutrophils bear two classes of receptors for GRO alpha, NAP-2, and IL-8 (p70 and p44) that may differ in their mode of interaction with GTP regulatory proteins. Guanosine Triphosphate 174-177 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 1415104-6 1992 The tyrosylprotein sulfotransferase enzyme required Triton X-100, MnCl2 and 5"-AMP, and obtained optimum activity at pH 6.8 in the presence of 0.5% Triton X-100, 20 mM MnCl2, 50 mM NaF, and 2 mM 5"-AMP. Octoxynol 52-64 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 1382479-1 1992 The objective of this study was to investigate the effect of interleukin-8 (IL-8) and RANTES on basophil histamine release induced with monocyte chemoattractant peptide-1 (MCP-1) and crude histamine releasing factor (HRF). Histamine 105-114 C-X-C motif chemokine ligand 8 Homo sapiens 61-74 1415104-6 1992 The tyrosylprotein sulfotransferase enzyme required Triton X-100, MnCl2 and 5"-AMP, and obtained optimum activity at pH 6.8 in the presence of 0.5% Triton X-100, 20 mM MnCl2, 50 mM NaF, and 2 mM 5"-AMP. manganese chloride 66-71 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 1415104-6 1992 The tyrosylprotein sulfotransferase enzyme required Triton X-100, MnCl2 and 5"-AMP, and obtained optimum activity at pH 6.8 in the presence of 0.5% Triton X-100, 20 mM MnCl2, 50 mM NaF, and 2 mM 5"-AMP. Adenosine Monophosphate 76-82 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 1382479-2 1992 IL-8 induced low levels of histamine release (8.5 +/- 0.5%) from basophils obtained from only six of 20 donors at high concentrations (10(-6) M). Histamine 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1415104-6 1992 The tyrosylprotein sulfotransferase enzyme required Triton X-100, MnCl2 and 5"-AMP, and obtained optimum activity at pH 6.8 in the presence of 0.5% Triton X-100, 20 mM MnCl2, 50 mM NaF, and 2 mM 5"-AMP. Octoxynol 148-160 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 1415104-6 1992 The tyrosylprotein sulfotransferase enzyme required Triton X-100, MnCl2 and 5"-AMP, and obtained optimum activity at pH 6.8 in the presence of 0.5% Triton X-100, 20 mM MnCl2, 50 mM NaF, and 2 mM 5"-AMP. manganese chloride 168-173 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 1415104-6 1992 The tyrosylprotein sulfotransferase enzyme required Triton X-100, MnCl2 and 5"-AMP, and obtained optimum activity at pH 6.8 in the presence of 0.5% Triton X-100, 20 mM MnCl2, 50 mM NaF, and 2 mM 5"-AMP. Adenosine Monophosphate 195-201 C-X-C motif chemokine ligand 8 Homo sapiens 181-184 1382479-4 1992 However, both IL-8 and RANTES inhibited MCP-1 and HRF-induced histamine release from basophils dose-dependently at concentrations of 10(-9) to 10(-7) M. Basophils from all donors showed a significant inhibitory response (greater than 15%). Histamine 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 1382479-9 1992 IL-8 inhibited histamine release induced with all three peaks of HRF. Histamine 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1382479-10 1992 The inhibition of histamine release by IL-8 was significantly higher in normal subjects than in allergic patients (59 +/- 9% versus 31 +/- 7%, P less than 0.05). Histamine 18-27 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 1522134-6 1992 Treatment of amnion cells stimulated by IL-1 beta with cycloheximide resulted in increased IL-8 production, while incubation of IL-1 beta treated amnion cells with actinomycin D resulted in a concentration-dependent decrease in detectable amounts of IL-8. Cycloheximide 55-68 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 1397489-9 1992 The enzyme shows a molecular weight of 57 kDa, is insensitive to NaF, hydrolyzes p-nitro-phenylphosphate and o-c-phenylphosphate; ATP, a-naphthyl-phosphate and beta-glycerolphosphate are also dephosphorylated. o-c-phenylphosphate 109-128 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 1522134-6 1992 Treatment of amnion cells stimulated by IL-1 beta with cycloheximide resulted in increased IL-8 production, while incubation of IL-1 beta treated amnion cells with actinomycin D resulted in a concentration-dependent decrease in detectable amounts of IL-8. Cycloheximide 55-68 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 1383379-10 1992 IL-8 inhibited this IgE production without affecting IgM, IgG1, IgG2, IgG3, IgG4, or IgA production, whereas IFN-gamma, IFN-alpha, or prostaglandin E2 (PGE2) failed to do so. Dinoprostone 152-156 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1522134-6 1992 Treatment of amnion cells stimulated by IL-1 beta with cycloheximide resulted in increased IL-8 production, while incubation of IL-1 beta treated amnion cells with actinomycin D resulted in a concentration-dependent decrease in detectable amounts of IL-8. Dactinomycin 164-177 C-X-C motif chemokine ligand 8 Homo sapiens 91-95 1522134-6 1992 Treatment of amnion cells stimulated by IL-1 beta with cycloheximide resulted in increased IL-8 production, while incubation of IL-1 beta treated amnion cells with actinomycin D resulted in a concentration-dependent decrease in detectable amounts of IL-8. Dactinomycin 164-177 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 1381398-6 1992 In contrast, two other neutrophil agonists 1-0-alkyl-2-acetyl sn-glycero-3-phosphocholine and granulocyte-macrophage-CSF, which, like IL-8, are produced by activated HUVEC, as well as the leukocyte-derived chemoattractant leukotriene B4, exerted minimal inhibitory effects on adhesion. 1-0-alkyl-2-acetyl sn-glycero-3-phosphocholine 43-89 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 1381398-6 1992 In contrast, two other neutrophil agonists 1-0-alkyl-2-acetyl sn-glycero-3-phosphocholine and granulocyte-macrophage-CSF, which, like IL-8, are produced by activated HUVEC, as well as the leukocyte-derived chemoattractant leukotriene B4, exerted minimal inhibitory effects on adhesion. Leukotriene B4 222-236 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 1325308-0 1992 Signal transduction pathways leading to the production of IL-8 by human monocytes are differentially regulated by dexamethasone. Dexamethasone 114-127 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 1325308-3 1992 We have now examined the effect of dexamethasone on the LPS-induced and other signal transduction pathways leading to the production of IL-8 by human monocytes. Dexamethasone 35-48 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 1325308-4 1992 Dexamethasone inhibited the production of IL-8 stimulated with a cyclic adenosine monophosphate analog or LPS. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 1325308-4 1992 Dexamethasone inhibited the production of IL-8 stimulated with a cyclic adenosine monophosphate analog or LPS. Cyclic AMP 65-95 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 1325308-6 1992 These results suggest that the signal transduction pathways leading to the production of IL-8 by human monocytes are differentially regulated by dexamethasone. Dexamethasone 145-158 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 1422951-1 1992 Clinical studies on the use of sodium fluoride (NaF) in osteoporotic patients have demonstrated increased spinal bone mass without a reduction in vertebral fracture incidence, and a trend towards reduced appendicular bone mass with an increase in peripheral fracture incidence. Sodium Fluoride 31-46 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 1477297-5 1992 Taken together, these results suggest that the stimulation of the IL-8 or gro beta receptor evokes three similar responses, but that only the activation of the IL-8 receptor and not that of gro beta results in elevated CD11b expression and calcium mobilization in human neutrophils. Calcium 240-247 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 1477297-5 1992 Taken together, these results suggest that the stimulation of the IL-8 or gro beta receptor evokes three similar responses, but that only the activation of the IL-8 receptor and not that of gro beta results in elevated CD11b expression and calcium mobilization in human neutrophils. Calcium 240-247 C-X-C motif chemokine ligand 8 Homo sapiens 160-164 1522234-5 1992 We now show that isolated human blood monocytes respond to such an oxygen stress with augmented production of IL-8. Oxygen 67-73 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 1522234-11 1992 The association of anoxic preconditioning and oxygen stress with augmented production of monocyte-derived IL-8 support the potential role for ischemia-reperfusion and hyperoxia-induced IL-8 production in vivo, providing a possible mechanism for PMN migration/activation in disease states characterized by altered tissue oxygenation. Oxygen 46-52 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 1522234-11 1992 The association of anoxic preconditioning and oxygen stress with augmented production of monocyte-derived IL-8 support the potential role for ischemia-reperfusion and hyperoxia-induced IL-8 production in vivo, providing a possible mechanism for PMN migration/activation in disease states characterized by altered tissue oxygenation. Oxygen 46-52 C-X-C motif chemokine ligand 8 Homo sapiens 185-189 1522286-0 1992 Distribution of fluoride in saliva and plaque fluid after a 0.048 mol/L NaF rinse. Fluorides 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 1325836-10 1992 However, when the phosphatase inhibitors NaF and sodium orthovanadate were included in the assay systems, phosphatidic acid was detected in addition to diradylglycerol. Phosphatidic Acids 106-123 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 1325836-10 1992 However, when the phosphatase inhibitors NaF and sodium orthovanadate were included in the assay systems, phosphatidic acid was detected in addition to diradylglycerol. diarachidonyl diglyceride 152-167 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 1323612-0 1992 Recombinant tumor necrosis factor-alpha potentiates neutrophil degranulation in response to host defense cytokines neutrophil-activating peptide 2 and IL-8 by modulating intracellular cyclic AMP levels. Cyclic AMP 184-194 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 1643627-4 1992 (a) IL-8 poly A+ mRNA was detected in 2 of 2 low grade astrocytomas, 1 of 2 anaplastic astrocytomas, and 6 of 6 glioblastomas. Poly A 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 1358240-3 1992 The drugs sodium aurothiomalate, D-penicillamine and sulphasalazine were all able to modulate IL-8 mRNA synthesis in and protein secretion from endothelial cells. Gold Sodium Thiomalate 10-31 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 1358240-3 1992 The drugs sodium aurothiomalate, D-penicillamine and sulphasalazine were all able to modulate IL-8 mRNA synthesis in and protein secretion from endothelial cells. Penicillamine 33-48 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 1358240-3 1992 The drugs sodium aurothiomalate, D-penicillamine and sulphasalazine were all able to modulate IL-8 mRNA synthesis in and protein secretion from endothelial cells. Sulfasalazine 53-67 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 1358240-5 1992 In endothelial cells, treatment with hydrocortisone led to a linear suppression of IL-8 production in concentrations ranging from 0.5 micrograms/ml up to 500 micrograms/ml. Hydrocortisone 37-51 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 1358240-7 1992 By contrast, 5-aminosalicylic acid induced a threefold increase in the IL-8 release. Mesalamine 13-34 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 1358240-8 1992 In peripheral blood mononuclear cells it was only possible to suppress the IL-8 production by hydrocortisone treatment. Hydrocortisone 94-108 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 1326018-1 1992 The effect of protease inhibitors on the intracellular production of free radicals was investigated by measuring chemiluminescence (CL) elicited from phagocytosed luminol-bound microspheres (Lumispheres) in human neutrophils stimulated with formylmethionyl-leucyl-phenylalanine (fMLP), interleukin-8 (IL-8), phorbol 12-myristate 13-acetate, or diacylglycerol. Free Radicals 69-82 C-X-C motif chemokine ligand 8 Homo sapiens 286-299 1326018-1 1992 The effect of protease inhibitors on the intracellular production of free radicals was investigated by measuring chemiluminescence (CL) elicited from phagocytosed luminol-bound microspheres (Lumispheres) in human neutrophils stimulated with formylmethionyl-leucyl-phenylalanine (fMLP), interleukin-8 (IL-8), phorbol 12-myristate 13-acetate, or diacylglycerol. Free Radicals 69-82 C-X-C motif chemokine ligand 8 Homo sapiens 301-305 1326018-3 1992 Compared to control buffer without protease inhibitor, gabexate mesylate (322 micrograms/ml) caused about a 10-fold increase in intracellular CL in stimulated neutrophils, and ulinastatin (3100 U/ml) a twofold increase in neutrophils stimulated with fMLP or IL-8. Gabexate 55-72 C-X-C motif chemokine ligand 8 Homo sapiens 258-262 1512465-0 1992 Interleukin-8 stimulates calcium transients and promotes epidermal cell proliferation. Calcium 25-32 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1512465-8 1992 Polyclonal anti-IL-8 antibody blocked IL-8-induced calcium changes and proliferation. Calcium 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 1512465-8 1992 Polyclonal anti-IL-8 antibody blocked IL-8-induced calcium changes and proliferation. Calcium 51-58 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 1392258-3 1992 A retrospective assessment was made of clinical data collected from our observations of 389 osteoporotics treated with fluoride 30 +/- 8 mg/day (mean +/- SD) (equivalent to 66 +/- 17 mg NaF/day) and calcium 1500 mg/day for 28 +/- 18 months. Fluorides 119-127 C-X-C motif chemokine ligand 8 Homo sapiens 186-189 1323613-0 1992 Retinoic acid and phorbol ester synergistically up-regulate IL-8 expression and specifically modulate protein kinase C-epsilon in human skin fibroblasts. Tretinoin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 1323613-0 1992 Retinoic acid and phorbol ester synergistically up-regulate IL-8 expression and specifically modulate protein kinase C-epsilon in human skin fibroblasts. Phorbol Esters 18-31 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 1323613-3 1992 TPA (as previously reported) and RA both induced IL-8 mRNA and protein in a time- and dose-dependent manner. Tretinoin 33-35 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 1323613-4 1992 IL-8 mRNA induction by TPA (10 nM) was maximal (15-fold) within 6 h, and returned to baseline within 24 h of treatment, although maximal induction (10-fold) by RA (1 microM) did not occur until 24 h posttreatment. Tretinoin 160-162 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1323613-5 1992 Induction of IL-8 by TPA was blocked by 1-(5-isoquinolinyl-sulfonyl)-2-methylpiperazine, which inhibits PKC and cAMP-dependent protein kinases (PKA), but not by N-(2-ganidinoethyl)-5-isoquinoline sulfonamide, which preferentially inhibits PKA, consistent with the participation of PKC in the induction of IL-8 by TPA. 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine 40-87 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 1323613-5 1992 Induction of IL-8 by TPA was blocked by 1-(5-isoquinolinyl-sulfonyl)-2-methylpiperazine, which inhibits PKC and cAMP-dependent protein kinases (PKA), but not by N-(2-ganidinoethyl)-5-isoquinoline sulfonamide, which preferentially inhibits PKA, consistent with the participation of PKC in the induction of IL-8 by TPA. 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine 40-87 C-X-C motif chemokine ligand 8 Homo sapiens 305-309 1323613-5 1992 Induction of IL-8 by TPA was blocked by 1-(5-isoquinolinyl-sulfonyl)-2-methylpiperazine, which inhibits PKC and cAMP-dependent protein kinases (PKA), but not by N-(2-ganidinoethyl)-5-isoquinoline sulfonamide, which preferentially inhibits PKA, consistent with the participation of PKC in the induction of IL-8 by TPA. n-(2-ganidinoethyl)-5-isoquinoline sulfonamide 161-207 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 1323613-6 1992 In contrast, induction of IL-8 by RA was inhibited by both 1-(5-isoquinoline sulfonamide and N-(2-gamidinoethyl)-5-isoquinoline sulfonamide, suggesting the participation of PKA in the induction of IL-8 by RA. Tretinoin 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 1323613-6 1992 In contrast, induction of IL-8 by RA was inhibited by both 1-(5-isoquinoline sulfonamide and N-(2-gamidinoethyl)-5-isoquinoline sulfonamide, suggesting the participation of PKA in the induction of IL-8 by RA. Tretinoin 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 1323613-6 1992 In contrast, induction of IL-8 by RA was inhibited by both 1-(5-isoquinoline sulfonamide and N-(2-gamidinoethyl)-5-isoquinoline sulfonamide, suggesting the participation of PKA in the induction of IL-8 by RA. 1-(5-isoquinoline sulfonamide 59-88 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 1323613-6 1992 In contrast, induction of IL-8 by RA was inhibited by both 1-(5-isoquinoline sulfonamide and N-(2-gamidinoethyl)-5-isoquinoline sulfonamide, suggesting the participation of PKA in the induction of IL-8 by RA. 1-(5-isoquinoline sulfonamide 59-88 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 1323613-6 1992 In contrast, induction of IL-8 by RA was inhibited by both 1-(5-isoquinoline sulfonamide and N-(2-gamidinoethyl)-5-isoquinoline sulfonamide, suggesting the participation of PKA in the induction of IL-8 by RA. n-(2-gamidinoethyl)-5-isoquinoline sulfonamide 93-139 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 1323613-6 1992 In contrast, induction of IL-8 by RA was inhibited by both 1-(5-isoquinoline sulfonamide and N-(2-gamidinoethyl)-5-isoquinoline sulfonamide, suggesting the participation of PKA in the induction of IL-8 by RA. n-(2-gamidinoethyl)-5-isoquinoline sulfonamide 93-139 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 1323613-6 1992 In contrast, induction of IL-8 by RA was inhibited by both 1-(5-isoquinoline sulfonamide and N-(2-gamidinoethyl)-5-isoquinoline sulfonamide, suggesting the participation of PKA in the induction of IL-8 by RA. Tretinoin 205-207 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 1323613-8 1992 Induction of IL-8 by RA also did not appear to be mediated indirectly through induction of IL-1, because addition of IL-1R antagonist did not block IL-8 induction by RA. Tretinoin 21-23 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 1323613-9 1992 RA and TPA added in combination synergistically enhanced expression of IL-8 mRNA, measured at 6 (2-fold) and 24 h (10-fold) posttreatment. Tretinoin 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 1497091-6 1992 In addition, when neutrophils were treated with cycloheximide, there was evidence for "superinduction" of steady-state levels of IL-8 mRNA and inhibition of antigenic IL-8 production. Cycloheximide 48-61 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 1497091-6 1992 In addition, when neutrophils were treated with cycloheximide, there was evidence for "superinduction" of steady-state levels of IL-8 mRNA and inhibition of antigenic IL-8 production. Cycloheximide 48-61 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 1503884-2 1992 Interleukin-8, released from mononuclear cells that have been exposed to urate and other crystals, is a potent chemotaxin and activator of neutrophils. Uric Acid 73-78 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1639472-4 1992 IL-8 is detected by enzyme-linked immunosorbent assay within 2 h of stimulation, with steady a increase in its level through 72 h. Further studies demonstrated that LPS could serve as a primary stimulus for the expression of IL-8, since LPS challenge in the presence of cycloheximide resulted in superinduction of bone marrow mononuclear cell-derived IL-8 mRNA. Cycloheximide 270-283 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1639472-4 1992 IL-8 is detected by enzyme-linked immunosorbent assay within 2 h of stimulation, with steady a increase in its level through 72 h. Further studies demonstrated that LPS could serve as a primary stimulus for the expression of IL-8, since LPS challenge in the presence of cycloheximide resulted in superinduction of bone marrow mononuclear cell-derived IL-8 mRNA. Cycloheximide 270-283 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 1639472-4 1992 IL-8 is detected by enzyme-linked immunosorbent assay within 2 h of stimulation, with steady a increase in its level through 72 h. Further studies demonstrated that LPS could serve as a primary stimulus for the expression of IL-8, since LPS challenge in the presence of cycloheximide resulted in superinduction of bone marrow mononuclear cell-derived IL-8 mRNA. Cycloheximide 270-283 C-X-C motif chemokine ligand 8 Homo sapiens 225-229 1506514-2 1992 Calcium uptake was measured by treatment of the model plaques with [45Ca]-CaCl2 solutions with or without NaF. Calcium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 1612748-7 1992 IL-8 levels appeared to correlate significantly with lactate levels and inversely with leukocyte and platelet numbers and mean arterial pressure. Lactic Acid 53-60 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1644918-5 1992 Binding between NAP-1 and antibody is strong, since 8 M urea at neutral or alkaline pH did not release NAP-1. Urea 56-60 C-X-C motif chemokine ligand 8 Homo sapiens 16-21 1644918-6 1992 However, at pH 2.0 in 9 M urea approximately 15% of the total NAP-1 could be dissociated from the complex. Urea 26-30 C-X-C motif chemokine ligand 8 Homo sapiens 62-67 1634507-4 1992 By thin layer chromatography and reverse-phase high pressure liquid chromatography, we demonstrated that PAF synthesized by human PMN stimulated with IL-8 is heterogeneous: the 2-acetylated phospholipids having the biological and physicochemical characteristics of PAF include the 1-O-alkyl form, which is produced in large extent (51%), and the 1-acyl form (20%). 2-acetylated phospholipids 177-203 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 1634507-4 1992 By thin layer chromatography and reverse-phase high pressure liquid chromatography, we demonstrated that PAF synthesized by human PMN stimulated with IL-8 is heterogeneous: the 2-acetylated phospholipids having the biological and physicochemical characteristics of PAF include the 1-O-alkyl form, which is produced in large extent (51%), and the 1-acyl form (20%). 1-hexadecyl-2-acetyl-glycero-3-phosphocholine 281-284 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 1634507-4 1992 By thin layer chromatography and reverse-phase high pressure liquid chromatography, we demonstrated that PAF synthesized by human PMN stimulated with IL-8 is heterogeneous: the 2-acetylated phospholipids having the biological and physicochemical characteristics of PAF include the 1-O-alkyl form, which is produced in large extent (51%), and the 1-acyl form (20%). alkyl 285-290 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 1325732-2 1992 In 0.5 mM external Ca2+, NaF inhibited PTH release and lowered the cAMP content by 50-70% of the effects attained with 3.0 mM Ca2+. Cyclic AMP 67-71 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 1325732-4 1992 It seems likely that NaF activates the inhibitory G1-protein involved in the regulation of cAMP generation. Cyclic AMP 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 1325732-6 1992 Inhibition of PTH release by NaF probably results from the combined effects on [Ca2+]i and cAMP content. Cyclic AMP 91-95 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 1422225-6 1992 rhIL-8 was assessed for biological efficacy by three criteria: (a) ability to induce chemotaxis in human neutrophils, (b) ability to induce oxygen burst metabolism, and (c) ability to be recognized by purified rabbit antibody generated against monocyte-derived IL-8. Oxygen 140-146 C-X-C motif chemokine ligand 8 Homo sapiens 2-6 1321178-0 1992 Protective effect of nedocromil sodium on the interleukin-1-induced production of interleukin-8 in human bronchial epithelial cells. Nedocromil 21-38 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 1321178-7 1992 Nedocromil sodium reduced the IL-1-induced release of IL-8 in a dose-dependent manner, but concentrations of the compounds, up to 10(-5) mol/L, did not affect the constitutive production of this cytokine. Nedocromil 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 1613466-3 1992 Although these proteins copurified with MCP-1 and IL-8 on heparin-Sepharose, they could be separated by cation-exchange fast protein liquid chromatography and reverse-phase high-performance liquid chromatography. Sepharose 66-75 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 1640174-2 1992 Pretreatment of neutrophils with cytochalasin B abolished the LAI effect of IL-8, suggesting a microfilament-dependent mechanism. Cytochalasin B 33-47 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 1322442-2 1992 An increase in the cytosolic free calcium concentration ([Ca2+]i) was greater in IL-8T- than in IL-8M- or IL-8E-activated HNs, and IL-8T was more potent than either IL-8M or IL-8E in sequentially desensitizing the HNs to the effects of the other IL-8 forms. Calcium 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 81-86 1322442-2 1992 An increase in the cytosolic free calcium concentration ([Ca2+]i) was greater in IL-8T- than in IL-8M- or IL-8E-activated HNs, and IL-8T was more potent than either IL-8M or IL-8E in sequentially desensitizing the HNs to the effects of the other IL-8 forms. Calcium 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 131-136 1322442-2 1992 An increase in the cytosolic free calcium concentration ([Ca2+]i) was greater in IL-8T- than in IL-8M- or IL-8E-activated HNs, and IL-8T was more potent than either IL-8M or IL-8E in sequentially desensitizing the HNs to the effects of the other IL-8 forms. Calcium 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 1322442-3 1992 IL-8 induced a time- and concentration-dependent (0.1-100 nM) increase in the production of inositol 1,4,5-trisphosphate (IP3) in HNs. Inositol 1,4,5-Trisphosphate 92-120 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1322442-3 1992 IL-8 induced a time- and concentration-dependent (0.1-100 nM) increase in the production of inositol 1,4,5-trisphosphate (IP3) in HNs. Inositol 1,4,5-Trisphosphate 122-125 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1322442-4 1992 U-73122 (1-[6-[[17 beta-3-methoxyestra-1,3,5(10)-trien-17- yl]amino]hexyl]-1H-pyrrole-2,5-dione), a potent inhibitor of phospholipase C-catalyzed events in HNs, suppressed IL-8-triggered IP3 production, increased [Ca2+]i and granule exocytosis in HNs. 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1322442-4 1992 U-73122 (1-[6-[[17 beta-3-methoxyestra-1,3,5(10)-trien-17- yl]amino]hexyl]-1H-pyrrole-2,5-dione), a potent inhibitor of phospholipase C-catalyzed events in HNs, suppressed IL-8-triggered IP3 production, increased [Ca2+]i and granule exocytosis in HNs. 1-[6-[[17 beta-3-methoxyestra-1,3,5(10)-trien-17- yl]amino]hexyl 9-73 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1322442-4 1992 U-73122 (1-[6-[[17 beta-3-methoxyestra-1,3,5(10)-trien-17- yl]amino]hexyl]-1H-pyrrole-2,5-dione), a potent inhibitor of phospholipase C-catalyzed events in HNs, suppressed IL-8-triggered IP3 production, increased [Ca2+]i and granule exocytosis in HNs. maleimide 75-95 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1640174-3 1992 Interleukin-8 induced a rapid increase (less than or equal to 15 s) in the polymerization of actin filaments in human neutrophils that was blocked by pretreatment with cytochalasin B. Cytochalasin B 168-182 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1640174-7 1992 We suggest that the ability of IL-8 and certain other leukocyte agonists to regulate the actin polymer network of neutrophils may play an important role in adhesive interactions with the vascular endothelium. Polymers 95-102 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 1591007-4 1992 In this study, we examine the role of amiloride for the regulation of AM-derived interleukin (IL)-8, tumor necrosis factor (TNF), IL-6, and IL-1 beta. Amiloride 38-47 C-X-C motif chemokine ligand 8 Homo sapiens 81-99 18965453-2 1992 Uranium(VI) is selectively separated and/or pre-concentrated from a volume up to 20 ml on an activated silica gel microcolumn (2 x 40 mm) from a medium of 0.03M EDTA, 0.06M tartrate, and/or 0.05M NaF at pH = 9.3. Uranium 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 196-199 1591007-5 1992 Amiloride in concentrations of 10(-4) to 10(-6) M, concentrations capable of being achieved in the distal airways via nebulization, were shown to inhibit lipopolysaccharide-stimulated, AM-derived IL-8 and TNF in both a time- and dose-dependent fashion. Amiloride 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 1591007-6 1992 In addition, 5-(N,N-hexamethylene) amiloride hydrochloride, an amiloride analogue with specific sodium channel antiport inhibition, resulted in a similar dose-dependent suppression of lipopolysaccharide-stimulated, AM-derived IL-8 production. 5-(n,n-hexamethylene) amiloride hydrochloride 13-58 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 1591007-6 1992 In addition, 5-(N,N-hexamethylene) amiloride hydrochloride, an amiloride analogue with specific sodium channel antiport inhibition, resulted in a similar dose-dependent suppression of lipopolysaccharide-stimulated, AM-derived IL-8 production. Amiloride 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 1591007-7 1992 Furthermore, the suppressive effect of amiloride appeared to be at the level of mRNA for IL-8, TNF, IL-1 beta, and IL-6, whereas steady-state levels of beta-actin mRNA remained unaltered. Amiloride 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 1597151-5 1992 Sodium fluoride (NaF)-stimulated IP accumulation was also inhibited by U-73122 (from 1539 +/- 132 dpm to 414 +/- 21 dpm) while LH release increased from 22.9 +/- 1.4% total cellular LH to 28.0 +/- 2.2%. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 1597151-5 1992 Sodium fluoride (NaF)-stimulated IP accumulation was also inhibited by U-73122 (from 1539 +/- 132 dpm to 414 +/- 21 dpm) while LH release increased from 22.9 +/- 1.4% total cellular LH to 28.0 +/- 2.2%. 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione 71-78 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 1597151-5 1992 Sodium fluoride (NaF)-stimulated IP accumulation was also inhibited by U-73122 (from 1539 +/- 132 dpm to 414 +/- 21 dpm) while LH release increased from 22.9 +/- 1.4% total cellular LH to 28.0 +/- 2.2%. Luteinizing Hormone 127-129 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 1597151-9 1992 These results demonstrate that GnRH- as well as NaF-stimulated LH release can be uncoupled from IP production calling to question the role of IP3 as a second messenger for GnRH-stimulated LH release. Luteinizing Hormone 63-65 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 1315831-8 1992 Lineweaver-Burk analysis of the kinetics of PIP kinase assayed in the presence of 0.03 to 0.7 mM ATP showed that 10 nM IL-8 increased the Vmax of the enzyme 38 to 70.5%, with no significant change in the apparent Km for ATP or for PIP. Adenosine Triphosphate 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 1631484-3 1992 More fluoride was deposited on the enamel from the neutral 2% NaF solution than from the Duraphat treatment. Fluorides 5-13 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 1631484-7 1992 Duraphat-treated samples submerged in water after the exposure lost only about 50% of the deposited fluoride, whereas samples treated with 2% NaF are known to lose all their fluoride under similar circumstances, a condition which may be related to the favorable clinical effect of Duraphat. Fluorides 174-182 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 1631484-7 1992 Duraphat-treated samples submerged in water after the exposure lost only about 50% of the deposited fluoride, whereas samples treated with 2% NaF are known to lose all their fluoride under similar circumstances, a condition which may be related to the favorable clinical effect of Duraphat. sodium fluoride topical preparation 281-289 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 1593135-2 1992 Since binding inhibition tests indicated that three monoclonal antibodies (mAbs; BS-1, WS-4, WS-6) blocked the binding of 125I-labelled IL-8 to neutrophils, we tested an ELISA using these mAbs as primary antibodies, rabbit anti-IL-8 Ab as the secondary antibody, and alkaline phosphatase-labelled goat anti-rabbit Ab as the conjugate. Tungsten 87-89 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 1593135-2 1992 Since binding inhibition tests indicated that three monoclonal antibodies (mAbs; BS-1, WS-4, WS-6) blocked the binding of 125I-labelled IL-8 to neutrophils, we tested an ELISA using these mAbs as primary antibodies, rabbit anti-IL-8 Ab as the secondary antibody, and alkaline phosphatase-labelled goat anti-rabbit Ab as the conjugate. Tungsten 93-95 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 1315831-8 1992 Lineweaver-Burk analysis of the kinetics of PIP kinase assayed in the presence of 0.03 to 0.7 mM ATP showed that 10 nM IL-8 increased the Vmax of the enzyme 38 to 70.5%, with no significant change in the apparent Km for ATP or for PIP. Adenosine Triphosphate 220-223 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 1315831-10 1992 The microfilament disrupter, cytochalasin b, inhibited IL-8 induced stimulation of PIP kinase. Cytochalasin B 29-43 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 1398515-5 1992 Supernatants of TPA-stimulated Co cells contained the cytokines IL2, IL3, IL4 and IL8, whereas these cytokines were not detected in the supernatants of untreated cells. Tetradecanoylphorbol Acetate 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 1578146-6 1992 IL-8 release was dependent on FMLP-induced de novo protein synthesis because it was inhibited by cycloheximide, was paralleled by enhanced expression of IL-8 mRNA and was potentiated from two- to sixfold after preincubation of PMN with cytochalasin B. Cycloheximide 97-110 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1578146-6 1992 IL-8 release was dependent on FMLP-induced de novo protein synthesis because it was inhibited by cycloheximide, was paralleled by enhanced expression of IL-8 mRNA and was potentiated from two- to sixfold after preincubation of PMN with cytochalasin B. Cytochalasin B 236-250 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1315244-4 1992 We show that 3 h pretreatment of pituitary cell cultures with 10 mM NaF (a G protein activator), resulted in decreased gonadotrope responsiveness to subsequent GnRH treatment (3 h, 100 nM; 34.4 +/- 1.6% vs. 23.4 +/- 1.5% of total cellular LH). Luteinizing Hormone 239-241 C-X-C motif chemokine ligand 8 Homo sapiens 68-71 1315244-5 1992 NaF-provoked gonadotrope desensitization to GnRH also occurred in the presence of 3 mM EGTA and in cells which had been depleted of protein kinase C. Desensitization to GnRH did not occur in response to pretreatment with (Bu)2cAMP (8 h, 1 mM). Egtazic Acid 87-91 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 1315244-5 1992 NaF-provoked gonadotrope desensitization to GnRH also occurred in the presence of 3 mM EGTA and in cells which had been depleted of protein kinase C. Desensitization to GnRH did not occur in response to pretreatment with (Bu)2cAMP (8 h, 1 mM). (bu)2camp 221-230 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 1315244-8 1992 In contrast, 3 h NaF (10 mM) pretreatment enhanced responsiveness of the gonadotrope to the Ca2+ ionophore A23187 in a protein kinase C- and cAMP-dependent manner. Calcimycin 107-113 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 1315244-8 1992 In contrast, 3 h NaF (10 mM) pretreatment enhanced responsiveness of the gonadotrope to the Ca2+ ionophore A23187 in a protein kinase C- and cAMP-dependent manner. Cyclic AMP 141-145 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 1315244-10 1992 These data suggest that G protein activation by NaF provokes gonadotrope desensitization to GnRH stimulation by both decreasing receptor numbers and by uncoupling of the receptors from inositol phosphate production. Inositol Phosphates 185-203 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 1556187-2 1992 We found that instillation of crocidolite asbestos into the pleural space of rabbits led to the appearance in pleural liquid of chemotactic activity for neutrophils, and that this chemotactic activity was inhibited significantly by a neutralizing antibody to human interleukin 8 (IL-8). Asbestos, Crocidolite 30-50 C-X-C motif chemokine ligand 8 Homo sapiens 265-278 1569349-5 1992 The IL-8 elevation, however, was remarkably suppressed by infusion of a steroid into the mother to promote fetal lung maturation. Steroids 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 1592440-0 1992 Molecular analysis of the inhibition of interleukin-8 production by dexamethasone in a human fibrosarcoma cell line. Dexamethasone 68-81 C-X-C motif chemokine ligand 8 Homo sapiens 40-53 1592440-1 1992 In order to analyse the effects of glucocorticoids on interleukin-8 (IL-8) production more precisely, we examined the effects of dexamethasone on IL-8 production at the molecular level in a human fibrosarcoma cell line, 8387, which IL-1 induces to express IL-8 messenger RNA (mRNA) and to secrete IL-8. Dexamethasone 129-142 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 1592440-1 1992 In order to analyse the effects of glucocorticoids on interleukin-8 (IL-8) production more precisely, we examined the effects of dexamethasone on IL-8 production at the molecular level in a human fibrosarcoma cell line, 8387, which IL-1 induces to express IL-8 messenger RNA (mRNA) and to secrete IL-8. Dexamethasone 129-142 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 1592440-1 1992 In order to analyse the effects of glucocorticoids on interleukin-8 (IL-8) production more precisely, we examined the effects of dexamethasone on IL-8 production at the molecular level in a human fibrosarcoma cell line, 8387, which IL-1 induces to express IL-8 messenger RNA (mRNA) and to secrete IL-8. Dexamethasone 129-142 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 1592440-2 1992 Over a wide dose range, dexamethasone inhibited IL-8 production induced by IL-1 alpha stimulation. Dexamethasone 24-37 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 1592440-3 1992 Northern blotting analysis showed that dexamethasone also inhibited the IL-8 mRNA accumulation in a similar dose-related manner. Dexamethasone 39-52 C-X-C motif chemokine ligand 8 Homo sapiens 72-76 1592440-4 1992 Nuclear run-off assay revealed that dexamethasone decreased the transcription of the IL-8 gene and the degree of inhibition of transcription correlated well with the inhibition of IL-8 production, suggesting that the action of glucocorticoids is mainly at the transcriptional level. Dexamethasone 36-49 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 1551879-4 1992 We have studied, by monitoring the activation-dependent tryptophan fluorescence of transducin T alpha subunit, the pF (-log[F-]) and pH dependencies of the kinetics of activation and deactivation of T alpha GDP in the presence of NaF and aluminum or beryllium salts. Guanosine Diphosphate 207-210 C-X-C motif chemokine ligand 8 Homo sapiens 230-233 1533644-4 1992 The addition of aluminium chloride to 15 microM reduced the concentration of NaF required for 50% inhibition to 0.76 +/- 0.21 mM (n = 10). Aluminum Chloride 16-34 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 1556187-2 1992 We found that instillation of crocidolite asbestos into the pleural space of rabbits led to the appearance in pleural liquid of chemotactic activity for neutrophils, and that this chemotactic activity was inhibited significantly by a neutralizing antibody to human interleukin 8 (IL-8). Asbestos, Crocidolite 30-50 C-X-C motif chemokine ligand 8 Homo sapiens 280-284 1315451-0 1992 Acquisition of alkali-soluble fluoride by enamel through treatment with NaF-containing toothpastes in vitro. Fluorides 30-38 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 1592976-3 1992 This micro-analytical technique was used for investigation of the effects of dentifrice formulations containing NaF, xylitol, or NaF/xylitol on plaque acid metabolism. plaque acid 144-155 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 1315451-1 1992 The first aim of the present study was to examine if alkali-soluble fluoride (calcium fluoride-like material and adsorbed fluoride) forms when a NaF-containing toothpaste is applied on human enamel surface in vitro. Fluorides 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 145-148 1315451-1 1992 The first aim of the present study was to examine if alkali-soluble fluoride (calcium fluoride-like material and adsorbed fluoride) forms when a NaF-containing toothpaste is applied on human enamel surface in vitro. Calcium Fluoride 78-94 C-X-C motif chemokine ligand 8 Homo sapiens 145-148 1315451-1 1992 The first aim of the present study was to examine if alkali-soluble fluoride (calcium fluoride-like material and adsorbed fluoride) forms when a NaF-containing toothpaste is applied on human enamel surface in vitro. Fluorides 86-94 C-X-C motif chemokine ligand 8 Homo sapiens 145-148 1315451-8 1992 The clinical effect of a NaF-containing toothpaste may thus well depend on an initial formation of alkali-soluble fluoride. Fluorides 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 1347804-4 1992 Choriodecidual cells in culture produced substantial amounts of interleukin-8; release was inhibited by progesterone and stimulated by the antiprogestagen mifepristone. Progesterone 104-116 C-X-C motif chemokine ligand 8 Homo sapiens 64-77 1347804-4 1992 Choriodecidual cells in culture produced substantial amounts of interleukin-8; release was inhibited by progesterone and stimulated by the antiprogestagen mifepristone. Mifepristone 155-167 C-X-C motif chemokine ligand 8 Homo sapiens 64-77 1347804-6 1992 Since prostaglandin E and interleukin-8 have synergistic effects, we suggest that interleukin-8 activity is the final common step of prostaglandin and antiprogestagen action in parturition. Prostaglandins E 6-21 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 1347804-6 1992 Since prostaglandin E and interleukin-8 have synergistic effects, we suggest that interleukin-8 activity is the final common step of prostaglandin and antiprogestagen action in parturition. Prostaglandins 6-19 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 1546956-8 1992 GTP[35S] binding to the membranes was also stimulated by two IL-8-related cytokines, neutrophil-activating peptide 2 (NAP-2) and melanoma growth-stimulatory activity (gro/MGSA). Guanosine Triphosphate 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 1540395-2 1992 Phorbol 12-myristate 13-acetate (PMA), alpha-thrombin, and sodium fluoride (NaF), a direct G-protein activator, produced a rapid and time-dependent translocation of PKC from the cytosol to the membrane. Tetradecanoylphorbol Acetate 0-31 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 1540395-2 1992 Phorbol 12-myristate 13-acetate (PMA), alpha-thrombin, and sodium fluoride (NaF), a direct G-protein activator, produced a rapid and time-dependent translocation of PKC from the cytosol to the membrane. Sodium Fluoride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 1540395-3 1992 Activation of PKC by brief pretreatment of human umbilical vein endothelial cell (HUVEC) monolayers with PMA resulted in the inhibition of NaF-induced inositol phosphate increases and attenuation of both alpha-thrombin- and NaF-activated increases in intracellular Ca2+ (Ca2+i). Tetradecanoylphorbol Acetate 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 1540395-3 1992 Activation of PKC by brief pretreatment of human umbilical vein endothelial cell (HUVEC) monolayers with PMA resulted in the inhibition of NaF-induced inositol phosphate increases and attenuation of both alpha-thrombin- and NaF-activated increases in intracellular Ca2+ (Ca2+i). Tetradecanoylphorbol Acetate 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 224-227 1540395-3 1992 Activation of PKC by brief pretreatment of human umbilical vein endothelial cell (HUVEC) monolayers with PMA resulted in the inhibition of NaF-induced inositol phosphate increases and attenuation of both alpha-thrombin- and NaF-activated increases in intracellular Ca2+ (Ca2+i). Inositol Phosphates 151-169 C-X-C motif chemokine ligand 8 Homo sapiens 139-142 1540395-8 1992 Staurosporine, a potent PKC inhibitor, at concentrations that inhibited PKC-induced phosphorylation of histone-1, augmented both alpha-thrombin- and NaF-induced production of inositol phosphates but markedly inhibited alpha-thrombin-, NaF-, and A23187-induced PGI2 synthesis. Staurosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 149-152 1540395-8 1992 Staurosporine, a potent PKC inhibitor, at concentrations that inhibited PKC-induced phosphorylation of histone-1, augmented both alpha-thrombin- and NaF-induced production of inositol phosphates but markedly inhibited alpha-thrombin-, NaF-, and A23187-induced PGI2 synthesis. Staurosporine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 235-238 1540395-8 1992 Staurosporine, a potent PKC inhibitor, at concentrations that inhibited PKC-induced phosphorylation of histone-1, augmented both alpha-thrombin- and NaF-induced production of inositol phosphates but markedly inhibited alpha-thrombin-, NaF-, and A23187-induced PGI2 synthesis. Inositol Phosphates 175-194 C-X-C motif chemokine ligand 8 Homo sapiens 149-152 1529797-0 1992 Interleukin-8 stimulates the formation of 15-hydroxy-eicosatetraenoic acid by human neutrophils in vitro. 15-hydroxy-eicosatetraenoic acid 42-74 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1529797-1 1992 Interleukin-8 (IL-8), is a potent activator of polymorphonuclear leukocyte (PMN) functions including chemotaxis, superoxide anion production, and enzyme release and it is also chemotactic for lymphocytes. Superoxides 113-129 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1529797-1 1992 Interleukin-8 (IL-8), is a potent activator of polymorphonuclear leukocyte (PMN) functions including chemotaxis, superoxide anion production, and enzyme release and it is also chemotactic for lymphocytes. Superoxides 113-129 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 1529797-2 1992 Additionally, it has recently been shown that IL-8 stimulates the formation of 5-lipoxygenase (LO) products of arachidonic acid (AA) by human PMNs. Arachidonic Acid 111-127 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 1529797-5 1992 Then IL-8 was added in biologically relevant concentrations ranging from 0.1 to 100 ng/ml and incubation was carried out for 5 min at 37 degrees C. Lipids were then extracted from supernatants, and eicosanoids were determined by quantitative RP-HPLC. Eicosanoids 198-209 C-X-C motif chemokine ligand 8 Homo sapiens 5-9 1546956-3 1992 To examine whether IL-8 receptors are coupled to activation of guanine-nucleotide-binding proteins (G-proteins), we have investigated the influence of IL-8 on GTP hydrolysis by and guanosine 5"-[gamma-[35S]thio]triphosphate (GTP[35S]) binding to purified human neutrophil plasma membranes. Guanosine Triphosphate 159-162 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 1546956-3 1992 To examine whether IL-8 receptors are coupled to activation of guanine-nucleotide-binding proteins (G-proteins), we have investigated the influence of IL-8 on GTP hydrolysis by and guanosine 5"-[gamma-[35S]thio]triphosphate (GTP[35S]) binding to purified human neutrophil plasma membranes. Guanosine Triphosphate 159-162 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 1546956-7 1992 High-affinity binding of GTP[35S] to neutrophil plasma membranes was stimulated half-maximally and maximally (up to 5-fold) by IL-8 at about 10 nM and 100 nM respectively. Guanosine Triphosphate 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 1546956-7 1992 High-affinity binding of GTP[35S] to neutrophil plasma membranes was stimulated half-maximally and maximally (up to 5-fold) by IL-8 at about 10 nM and 100 nM respectively. Sulfur-35 29-32 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 1546956-8 1992 GTP[35S] binding to the membranes was also stimulated by two IL-8-related cytokines, neutrophil-activating peptide 2 (NAP-2) and melanoma growth-stimulatory activity (gro/MGSA). Sulfur-35 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 1505106-4 1992 The results showed a significant increase in NAP-1 production by synovial fluid MC when compared to peripheral blood MC. Methylcholanthrene 80-82 C-X-C motif chemokine ligand 8 Homo sapiens 45-50 1617494-2 1992 As the bioavailability of sodium fluoride (NaF) can be impaired by concomitant absorption of calcium, both drugs have to be ingested separately. Sodium Fluoride 26-41 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 1617494-2 1992 As the bioavailability of sodium fluoride (NaF) can be impaired by concomitant absorption of calcium, both drugs have to be ingested separately. Calcium 93-100 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 1732379-11 1992 The observed ability of dapsone to inhibit neutrophil chemotaxis under agarose to FMLP and interleukin-8 may also be explained by interference with integrin-mediated adherence required for motility in this assay system. Dapsone 24-31 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 1547561-5 1992 When a combination of NaF and mannose was used, the blood glucose concentration was relatively stable but slightly higher than nonpreserved samples for the next 24 h. However, samples containing mannose were unsuitable for electrolyte analysis. Glucose 58-65 C-X-C motif chemokine ligand 8 Homo sapiens 22-25 1547561-6 1992 We conclude that a combination of D-mannose and NaF may be a better preservative for blood glucose than either compound alone. Glucose 91-98 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 1518180-7 1992 Inositol metabolism and Ca mobilization in response to thrombin, STA2, or NaF were also investigated in patient A,B, and impaired aggregation to A23187 in patient C. The responses were normal in patient A, suggested that CO activity did not affect them. Inositol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 1728298-0 1992 Regulation of human alveolar macrophage- and blood monocyte-derived interleukin-8 by prostaglandin E2 and dexamethasone. Dinoprostone 85-101 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 1309557-14 1992 Stimulated mesothelial cells also expressed an inducible mRNA transcript that hybridized with a specific oligonucleotide probe for human NAP-1/IL-8. Oligonucleotides 105-120 C-X-C motif chemokine ligand 8 Homo sapiens 137-142 1309557-14 1992 Stimulated mesothelial cells also expressed an inducible mRNA transcript that hybridized with a specific oligonucleotide probe for human NAP-1/IL-8. Oligonucleotides 105-120 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 1729366-7 1992 Metabolically labeled IL-1 beta-stimulated chondrocytes synthesize IL-8 de novo, which comigrates on SDS-PAGE with IL-8 produced by synovial fibroblasts. Sodium Dodecyl Sulfate 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 1728298-0 1992 Regulation of human alveolar macrophage- and blood monocyte-derived interleukin-8 by prostaglandin E2 and dexamethasone. Dexamethasone 106-119 C-X-C motif chemokine ligand 8 Homo sapiens 68-81 1728298-4 1992 In this investigation, we describe the effects of prostaglandin E2 (PGE2) and dexamethasone (Dex) on IL-8 mRNA and protein expression from lipopolysaccharide (LPS)-treated human peripheral blood monocytes (PBM) and alveolar macrophages (AM). Dinoprostone 50-66 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 1728298-4 1992 In this investigation, we describe the effects of prostaglandin E2 (PGE2) and dexamethasone (Dex) on IL-8 mRNA and protein expression from lipopolysaccharide (LPS)-treated human peripheral blood monocytes (PBM) and alveolar macrophages (AM). Dinoprostone 68-72 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 1728298-4 1992 In this investigation, we describe the effects of prostaglandin E2 (PGE2) and dexamethasone (Dex) on IL-8 mRNA and protein expression from lipopolysaccharide (LPS)-treated human peripheral blood monocytes (PBM) and alveolar macrophages (AM). Dexamethasone 78-91 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 1728298-4 1992 In this investigation, we describe the effects of prostaglandin E2 (PGE2) and dexamethasone (Dex) on IL-8 mRNA and protein expression from lipopolysaccharide (LPS)-treated human peripheral blood monocytes (PBM) and alveolar macrophages (AM). Dexamethasone 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 1728298-5 1992 We demonstrate the dose-dependent suppression of IL-8 from LPS-stimulated PBM by PGE2. Dinoprostone 81-85 C-X-C motif chemokine ligand 8 Homo sapiens 49-53 1728298-6 1992 Treatment of stimulated PBM with 10(-6) M PGE2 resulted in maximal inhibition, causing 60% suppression of both IL-8 mRNA and extracellular protein levels. pbm 24-27 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 1728298-6 1992 Treatment of stimulated PBM with 10(-6) M PGE2 resulted in maximal inhibition, causing 60% suppression of both IL-8 mRNA and extracellular protein levels. Dinoprostone 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 1728298-8 1992 Treatment of LPS-stimulated PBM and AM with Dex (10(-6) to 10(-8) M) resulted in 75% decline in IL-8 mRNA and extracellular protein from either cell population. Dexamethasone 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 1728298-9 1992 Pretreatment of PBM with PGE2 or Dex 1 or 2 h before LPS stimulation caused a significant suppression of steady-state IL-8 mRNA levels; however, administration of either of these modulators 1 or 2 h after LPS stimulation failed to have an inhibitory effect. pbm 16-19 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 1728298-9 1992 Pretreatment of PBM with PGE2 or Dex 1 or 2 h before LPS stimulation caused a significant suppression of steady-state IL-8 mRNA levels; however, administration of either of these modulators 1 or 2 h after LPS stimulation failed to have an inhibitory effect. Dinoprostone 25-29 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 1728298-9 1992 Pretreatment of PBM with PGE2 or Dex 1 or 2 h before LPS stimulation caused a significant suppression of steady-state IL-8 mRNA levels; however, administration of either of these modulators 1 or 2 h after LPS stimulation failed to have an inhibitory effect. Dexamethasone 33-36 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 1511463-9 1992 Supernatants from OK432-stimulated mononuclear cells, as determined by enzyme-linked immunosorbent assays and radioimmunoassays, contained high levels of interleukin-8 (IL-8; 1567 +/- 145 pg/ml) and tumor necrosis factor (TNF alpha; 2105 +/- 152 pg/ml), low levels of leukotriene B4 (800 +/- 45 pg/ml) and IL-1 beta (180 +/- 22 pg/ml), but interferon gamma was not detectable. Leukotriene B4 268-282 C-X-C motif chemokine ligand 8 Homo sapiens 154-167 1370208-4 1992 Dexamethasone (1 mumol/L) concordantly repressed expression of GM-CSF, NAP-1/IL-8 and IL-6. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 71-76 1370208-4 1992 Dexamethasone (1 mumol/L) concordantly repressed expression of GM-CSF, NAP-1/IL-8 and IL-6. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 77-81 1370208-9 1992 Further experiments showed that dexamethasone downregulates expression of GM-CSF, NAP-1/IL-8, and IL-6 mainly by decreasing the mRNA stability of these cytokines, and that the dexamethasone-mediated repression of cytokine expression depends on ongoing protein and RNA syntheses. Dexamethasone 32-45 C-X-C motif chemokine ligand 8 Homo sapiens 82-87 1370208-9 1992 Further experiments showed that dexamethasone downregulates expression of GM-CSF, NAP-1/IL-8, and IL-6 mainly by decreasing the mRNA stability of these cytokines, and that the dexamethasone-mediated repression of cytokine expression depends on ongoing protein and RNA syntheses. Dexamethasone 32-45 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 1370208-9 1992 Further experiments showed that dexamethasone downregulates expression of GM-CSF, NAP-1/IL-8, and IL-6 mainly by decreasing the mRNA stability of these cytokines, and that the dexamethasone-mediated repression of cytokine expression depends on ongoing protein and RNA syntheses. Dexamethasone 176-189 C-X-C motif chemokine ligand 8 Homo sapiens 82-87 1370208-9 1992 Further experiments showed that dexamethasone downregulates expression of GM-CSF, NAP-1/IL-8, and IL-6 mainly by decreasing the mRNA stability of these cytokines, and that the dexamethasone-mediated repression of cytokine expression depends on ongoing protein and RNA syntheses. Dexamethasone 176-189 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 1425895-1 1992 Sodium fluoride (NaF) is used in the treatment of axial osteoporosis and so is mostly given to old patients. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 1423439-4 1992 Under the pH cycling conditions of the present study, the NaF dentifrice and mouthwash were observed to have a considerably higher uptake of fluoride in the lesion than the MFP dentifrice. Fluorides 141-149 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 1309871-3 1992 Moreover, postreceptor stimulation of superoxide production by NaF (a G protein activator), but not by phorbol myristate acetate, was significantly inhibited by SC-41930, indicating that SC-41930 may act via attenuation of a G protein-mediated signal transduction. Superoxides 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 1537591-3 1992 Co-incubation of neutrophils with neomycin and the direct G-protein activator sodium fluoride (NaF) resulted in an enhanced leukotriene formation at 0.5 mM neomycin and an inhibition at a concentration of 10 mM. Neomycin 34-42 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 1537591-3 1992 Co-incubation of neutrophils with neomycin and the direct G-protein activator sodium fluoride (NaF) resulted in an enhanced leukotriene formation at 0.5 mM neomycin and an inhibition at a concentration of 10 mM. Sodium Fluoride 78-93 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 1537591-3 1992 Co-incubation of neutrophils with neomycin and the direct G-protein activator sodium fluoride (NaF) resulted in an enhanced leukotriene formation at 0.5 mM neomycin and an inhibition at a concentration of 10 mM. Leukotrienes 124-135 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 1537591-3 1992 Co-incubation of neutrophils with neomycin and the direct G-protein activator sodium fluoride (NaF) resulted in an enhanced leukotriene formation at 0.5 mM neomycin and an inhibition at a concentration of 10 mM. Neomycin 156-164 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 1537591-5 1992 However, pretreatment of neutrophils with 10 mM neomycin followed by the addition of NaF or FMLP resulted in an enhanced generation of leukotrienes. Leukotrienes 135-147 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 1740648-0 1992 Heterogeneity in the mobilization of cytoplasmic calcium by human polymorphonuclear leukocytes in response to fMLP, C5a and IL-8/NAP-1. Calcium 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 1740648-0 1992 Heterogeneity in the mobilization of cytoplasmic calcium by human polymorphonuclear leukocytes in response to fMLP, C5a and IL-8/NAP-1. Calcium 49-56 C-X-C motif chemokine ligand 8 Homo sapiens 129-134 1726709-1 1991 Interleukin-8 (IL-8) stimulated an increase in cytoplasmic-free Ca2+ ([Ca2+]i) and intracellular pH (pHi) in parallel at low concentrations (0.5 to 5 ng/mL), and stimulated O2- release and membrane depolarization in parallel at high concentrations (50 to 5,000 ng/mL). Oxygen 173-175 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1720306-0 1991 Induction of members of the IL-8/NAP-1 gene family in human T lymphocytes is suppressed by cyclosporin A. Cyclosporine 91-104 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 1720306-0 1991 Induction of members of the IL-8/NAP-1 gene family in human T lymphocytes is suppressed by cyclosporin A. Cyclosporine 91-104 C-X-C motif chemokine ligand 8 Homo sapiens 33-38 1726709-4 1991 In addition, IL-8 was found to be a potent priming agent and to enhance O2- release stimulated by FMLP. Oxygen 72-74 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 1439483-0 1992 Interleukin-8 in inflammatory rheumatic diseases: synovial fluid levels, relation to rheumatoid factors, production by mononuclear cells, and effects of gold sodium thiomalate and methotrexate. Gold Sodium Thiomalate 153-175 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1439483-5 1992 Gold sodium thiomalate (GST) and methotrexate (MTX) inhibited the spontaneous and stimulated IL-8 production by PBMC by 55-86% at 50 and 10 micrograms/ml, respectively. Gold Sodium Thiomalate 0-22 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 1439483-5 1992 Gold sodium thiomalate (GST) and methotrexate (MTX) inhibited the spontaneous and stimulated IL-8 production by PBMC by 55-86% at 50 and 10 micrograms/ml, respectively. Methotrexate 33-45 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 1439483-5 1992 Gold sodium thiomalate (GST) and methotrexate (MTX) inhibited the spontaneous and stimulated IL-8 production by PBMC by 55-86% at 50 and 10 micrograms/ml, respectively. Methotrexate 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 1439483-6 1992 Two main conclusions were drawn: (1) rheumatoid factors appeared to be a major cause of enhanced IL-8 production in seropositive RA, and (2) inhibition of IL-8-mediated neutrophil migration and activation could be part of the mechanism of action of GST and MTX. Methotrexate 257-260 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 1492198-3 1992 The mentioned fact supported authors to study the impact of short-term 24 hrs sodium fluoride (NaF) action in concentration range of 0-500 mg.1(-1) drinking water in the frame of so-called minimal testing set (analysis of chromosomal aberrations in human peripheral lymphocytes, Ames test). Sodium Fluoride 78-93 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 1492198-3 1992 The mentioned fact supported authors to study the impact of short-term 24 hrs sodium fluoride (NaF) action in concentration range of 0-500 mg.1(-1) drinking water in the frame of so-called minimal testing set (analysis of chromosomal aberrations in human peripheral lymphocytes, Ames test). Drinking Water 148-162 C-X-C motif chemokine ligand 8 Homo sapiens 95-98 1492198-7 1992 Yet one order higher NaF concentration than its application norm 1 mg.l-1 (i.e. 11 mg.l-1) has induced the occurrence of 3.8% ABB after single addition for 24 hrs to the "healthy" blood cultivated in vitro at short-term. ABB 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 1492198-10 1992 Thus the two orders higher NaF concentration (110.0 mg.l-1) resulted in a strong increase of cells with chromosomal aberrations for all of indicators observed; e.g. 27.5% ABB. ABB 171-174 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 1958385-7 1991 The adherence of Am resulted in the induction of de novo IL-8 mRNA synthesis, as this mRNA accumulation was completely abrogated by actinomycin D. Dactinomycin 132-145 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 1774379-6 1991 Two recently isolated fluoride-resistant S. mutans strains produced more lactate and demineralized enamel more than did two recently isolated S. mutans strains from normal human subjects, both in the presence of 0 and 0.05 mmol/L NaF. Fluorides 22-30 C-X-C motif chemokine ligand 8 Homo sapiens 230-233 1726709-1 1991 Interleukin-8 (IL-8) stimulated an increase in cytoplasmic-free Ca2+ ([Ca2+]i) and intracellular pH (pHi) in parallel at low concentrations (0.5 to 5 ng/mL), and stimulated O2- release and membrane depolarization in parallel at high concentrations (50 to 5,000 ng/mL). Oxygen 173-175 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 1726709-2 1991 IL-8-induced O2- release was potentiated by tumor necrosis factor (TNF), granulocyte-macrophage colony-stimulating factor (GM-CSF), and granulocyte-CSF (G-CSF) in a dose-dependent manner, whereas it was inhibited by cyclic AMP agonists. Cyclic AMP 216-226 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1663497-2 1991 Diazepam also inhibited the superoxide production induced by FMLP, NaF, and A23187, but not that induced by PMA whose stimulant action was insensitive even to 10(-4) M diazepam. Diazepam 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 1665748-11 1991 Addition of 10 mM NaF at the plateau phase of [3H]-IP1 accumulation induced by 1 mM histamine resulted in a further increase in the level of [3H]-IP1. Tritium 47-49 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1665748-11 1991 Addition of 10 mM NaF at the plateau phase of [3H]-IP1 accumulation induced by 1 mM histamine resulted in a further increase in the level of [3H]-IP1. Isopenicillin N 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1665748-11 1991 Addition of 10 mM NaF at the plateau phase of [3H]-IP1 accumulation induced by 1 mM histamine resulted in a further increase in the level of [3H]-IP1. Histamine 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1665748-11 1991 Addition of 10 mM NaF at the plateau phase of [3H]-IP1 accumulation induced by 1 mM histamine resulted in a further increase in the level of [3H]-IP1. Tritium 142-144 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1665748-11 1991 Addition of 10 mM NaF at the plateau phase of [3H]-IP1 accumulation induced by 1 mM histamine resulted in a further increase in the level of [3H]-IP1. Isopenicillin N 146-149 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1665748-12 1991 The level of [3H]-IP1 in the presence of histamine + NaF was 1.4 +/- 0.2 fold of that of the sum of the responses to histamine and NaF acting alone (basal levels subtracted). [3h]-ip1 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 1665748-12 1991 The level of [3H]-IP1 in the presence of histamine + NaF was 1.4 +/- 0.2 fold of that of the sum of the responses to histamine and NaF acting alone (basal levels subtracted). [3h]-ip1 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 1752461-4 1991 NaF stimulated adenylate cyclase activity was inhibited by 50% at 2.5 mmol/l EGTA. Egtazic Acid 77-81 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 1663497-2 1991 Diazepam also inhibited the superoxide production induced by FMLP, NaF, and A23187, but not that induced by PMA whose stimulant action was insensitive even to 10(-4) M diazepam. Superoxides 28-38 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 1960255-4 1991 Results showed that lesions treated with the triclosan-fluoride product were remineralized 18.0 +/- 23.4% compared with 19.0 +/- 32.3% from a 1100-ppm F (NaF) positive control. triclosan-fluoride 45-63 C-X-C motif chemokine ligand 8 Homo sapiens 154-157 1723766-6 1991 Treatment with NaF/AlCl3, which uncouples G protein-mediated responses, caused significant attenuation of the relaxation responses to ADO, NECA, and CAD. Aluminum Chloride 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 15-18 1664043-1 1991 The interaction of the vitamin D receptor with a vitamin D-responsive element (VDRE) derived from the human osteocalcin promoter in vitro has been shown to require a nuclear accessory factor (NAF) derived from monkey kidney cells. Vitamin D 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 1664043-7 1991 NAF is a protein of 55 kDa, as assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and cross-linking experiments suggest that the VDR and NAF together form a heterodimer on a single VDRE with a mol wt of 103 kDa. Sodium Dodecyl Sulfate 43-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 1664043-7 1991 NAF is a protein of 55 kDa, as assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and cross-linking experiments suggest that the VDR and NAF together form a heterodimer on a single VDRE with a mol wt of 103 kDa. polyacrylamide 66-80 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 1800124-0 1991 Stimulation of miniature end-plate potential frequency by fluoride may involve activation of protein kinase C. NaF caused a dose-dependent rise in miniature end-plate potential (MEPP) frequency at the frog neuromuscular junction. Fluorides 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 1660854-2 1991 Similar data were observed for the direct G-protein activator sodium fluoride (NaF). Sodium Fluoride 62-77 C-X-C motif chemokine ligand 8 Homo sapiens 79-82 1681733-5 1991 Using the same antibody, IL-8 was immunoprecipitated from the supernatants of TNF-stimulated 35S-labelled keratinocytes, and a single 7-kd band product detected by SDS-PAGE. Sulfur-35 93-96 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 1681733-5 1991 Using the same antibody, IL-8 was immunoprecipitated from the supernatants of TNF-stimulated 35S-labelled keratinocytes, and a single 7-kd band product detected by SDS-PAGE. Sodium Dodecyl Sulfate 164-167 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 1681733-6 1991 In keeping with these biological activities and protein data, Northern blot analysis of total cellular RNA extracted from keratinocyte monolayers hybridized with a 32P-labelled 1-kb cDNA to IL-8 mRNA, revealed induction of the IL-8 gene in the presence of TNF-alpha and IL-1 beta, but not IFN-gamma. Phosphorus-32 164-167 C-X-C motif chemokine ligand 8 Homo sapiens 190-194 1681733-6 1991 In keeping with these biological activities and protein data, Northern blot analysis of total cellular RNA extracted from keratinocyte monolayers hybridized with a 32P-labelled 1-kb cDNA to IL-8 mRNA, revealed induction of the IL-8 gene in the presence of TNF-alpha and IL-1 beta, but not IFN-gamma. Phosphorus-32 164-167 C-X-C motif chemokine ligand 8 Homo sapiens 227-231 1918013-1 1991 In order to identify residues required for the binding of interleukin-8 (IL-8) to its receptor, mutants were constructed in which clusters of charged amino acids were systematically replaced with alanine along the entire IL-8 sequence. Alanine 196-203 C-X-C motif chemokine ligand 8 Homo sapiens 58-71 1918013-1 1991 In order to identify residues required for the binding of interleukin-8 (IL-8) to its receptor, mutants were constructed in which clusters of charged amino acids were systematically replaced with alanine along the entire IL-8 sequence. Alanine 196-203 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 1918013-2 1991 The mutants were tested for their ability to induce a receptor-mediated rise in cytosolic free Ca2+, a property of wild-type IL-8 which can readily be detected by flow cytometry using neutrophils loaded with the calcium probe Indo-1. Calcium 212-219 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 1918955-6 1991 Moreover, RA synovial fluid chemotactic activity for PMN in these fluids was inhibited 40 +/- 5% upon incubation with neutralizing polyclonal antibody to IL-8. Radium 10-12 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 1918955-12 1991 These results suggest that macrophage-derived IL-8 may play an important role in the recruitment of PMN in synovial inflammation associated with RA. Radium 145-147 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 1930284-7 1991 Analysis of inhibition kinetics further showed that (a) the reversible inhibition of both ComEst and MonEst by sodium fluoride (NaF) was noncompetitive (with Ki values of 1.28 and 0.01 mM, respectively, indicating a marked difference in sensitivity); (b) the inhibition of MonEst by PMSF was of "mixed" noncompetitive-competitive type; and (c) that DEPC exerted noncompetitive inhibition with similar Ki values (0.05 mM) for both esterase species. Sodium Fluoride 111-126 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 1930284-7 1991 Analysis of inhibition kinetics further showed that (a) the reversible inhibition of both ComEst and MonEst by sodium fluoride (NaF) was noncompetitive (with Ki values of 1.28 and 0.01 mM, respectively, indicating a marked difference in sensitivity); (b) the inhibition of MonEst by PMSF was of "mixed" noncompetitive-competitive type; and (c) that DEPC exerted noncompetitive inhibition with similar Ki values (0.05 mM) for both esterase species. Phenylmethylsulfonyl Fluoride 283-287 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 1653806-13 1991 Cyclosporines partially inhibited O2- formations induced by NaF and gamma-hexachlorocyclohexane. Cyclosporins 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 1911878-6 1991 On the other hand, with agonists that can by-pass (at least partially) the receptor-transductor-effector sequence, such as high-dose thrombin, PMA, NaF, only the exposure of fibrinogen receptors is blocked by ajoene. ajoene 209-215 C-X-C motif chemokine ligand 8 Homo sapiens 148-151 1653806-13 1991 Cyclosporines partially inhibited O2- formations induced by NaF and gamma-hexachlorocyclohexane. Superoxides 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 1716285-0 1991 IL-8 inhibits histamine release from human basophils induced by histamine-releasing factors, connective tissue activating peptide III, and IL-3. Histamine 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1891716-2 1991 Neutrophils express receptors for IL-8 that are coupled to guanine nucleotide-binding proteins (G proteins); binding of IL-8 to its receptor induces the mobilization of intracellular calcium stores. Calcium 183-190 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 1716285-2 1991 We now report the effect of IL-8 upon HRF-, connective tissue activating peptide III (CTAP III)-, and IL-3-induced histamine release from human basophils. Histamine 115-124 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 1716285-4 1991 When basophils were preincubated with IL-8 (10(-7) to 10(-11) M) for 5 min, followed by a 40-min incubation with HRF, histamine release was significantly inhibited in 20 of 25 donors. Histamine 118-127 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 1716285-5 1991 Inhibition was observed at as little as 10(-11) M IL-8, with maximal inhibition being attained at 10(-9) M. HRF-containing supernatants contain a mixture of different histamine-releasing moieties. Histamine 167-176 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 1716285-7 1991 Histamine release produced by two different HRF-containing chromatographic fractions (HRFvoid and HRFpeak 2) and purified CTAP-III (5 micrograms/ml) was inhibited by IL-8 in 10 of 12 donors, three of three donors, and seven of 10 donors, respectively. Histamine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 1716285-8 1991 IL-3 (5000 U/ml)-dependent histamine release was inhibited by IL-8 in all subjects tested. Histamine 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 1840701-6 1991 Mammalian cells transfected with the IL-8 receptor cDNA clone bind IL-8 with high affinity and respond specifically to IL-8 by transiently mobilizing calcium. Calcium 150-157 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 1840701-6 1991 Mammalian cells transfected with the IL-8 receptor cDNA clone bind IL-8 with high affinity and respond specifically to IL-8 by transiently mobilizing calcium. Calcium 150-157 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 1840701-6 1991 Mammalian cells transfected with the IL-8 receptor cDNA clone bind IL-8 with high affinity and respond specifically to IL-8 by transiently mobilizing calcium. Calcium 150-157 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 1922513-2 1991 When blood was preserved in microtest tubes coated with sodium fluoride (NaF) and measured after 1 hour at room temperature, the glucose level decreased by 7 to 36%. Sodium Fluoride 56-71 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 1922513-2 1991 When blood was preserved in microtest tubes coated with sodium fluoride (NaF) and measured after 1 hour at room temperature, the glucose level decreased by 7 to 36%. Glucose 129-136 C-X-C motif chemokine ligand 8 Homo sapiens 73-76 1891716-2 1991 Neutrophils express receptors for IL-8 that are coupled to guanine nucleotide-binding proteins (G proteins); binding of IL-8 to its receptor induces the mobilization of intracellular calcium stores. Calcium 183-190 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 1856599-6 1991 Antigenic and bioactive IL-8 were significantly apparent by 4-8 h, respectively, and increased significantly to maximal levels by 24 h. Furthermore, adherent PBMC IL-8 gene expression was suppressed by either concomitant treatment with actinomycin-D or cycloheximide, yet specific neutralizing antibodies directed against either IL-1 beta or tumor necrosis factor (TNF)-alpha failed to alter adherence-induced steady-state IL-8 mRNA levels. Dactinomycin 236-249 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 1939046-0 1991 Effect of sodium lauryl sulfate on the uptake of fluoride from NaF and MFP by etched enamel in vitro. Sodium Dodecyl Sulfate 10-31 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 1939046-0 1991 Effect of sodium lauryl sulfate on the uptake of fluoride from NaF and MFP by etched enamel in vitro. Fluorides 49-57 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 1856599-6 1991 Antigenic and bioactive IL-8 were significantly apparent by 4-8 h, respectively, and increased significantly to maximal levels by 24 h. Furthermore, adherent PBMC IL-8 gene expression was suppressed by either concomitant treatment with actinomycin-D or cycloheximide, yet specific neutralizing antibodies directed against either IL-1 beta or tumor necrosis factor (TNF)-alpha failed to alter adherence-induced steady-state IL-8 mRNA levels. Dactinomycin 236-249 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 1856599-6 1991 Antigenic and bioactive IL-8 were significantly apparent by 4-8 h, respectively, and increased significantly to maximal levels by 24 h. Furthermore, adherent PBMC IL-8 gene expression was suppressed by either concomitant treatment with actinomycin-D or cycloheximide, yet specific neutralizing antibodies directed against either IL-1 beta or tumor necrosis factor (TNF)-alpha failed to alter adherence-induced steady-state IL-8 mRNA levels. Dactinomycin 236-249 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 1856599-6 1991 Antigenic and bioactive IL-8 were significantly apparent by 4-8 h, respectively, and increased significantly to maximal levels by 24 h. Furthermore, adherent PBMC IL-8 gene expression was suppressed by either concomitant treatment with actinomycin-D or cycloheximide, yet specific neutralizing antibodies directed against either IL-1 beta or tumor necrosis factor (TNF)-alpha failed to alter adherence-induced steady-state IL-8 mRNA levels. Cycloheximide 253-266 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 1856599-6 1991 Antigenic and bioactive IL-8 were significantly apparent by 4-8 h, respectively, and increased significantly to maximal levels by 24 h. Furthermore, adherent PBMC IL-8 gene expression was suppressed by either concomitant treatment with actinomycin-D or cycloheximide, yet specific neutralizing antibodies directed against either IL-1 beta or tumor necrosis factor (TNF)-alpha failed to alter adherence-induced steady-state IL-8 mRNA levels. Cycloheximide 253-266 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 1856599-6 1991 Antigenic and bioactive IL-8 were significantly apparent by 4-8 h, respectively, and increased significantly to maximal levels by 24 h. Furthermore, adherent PBMC IL-8 gene expression was suppressed by either concomitant treatment with actinomycin-D or cycloheximide, yet specific neutralizing antibodies directed against either IL-1 beta or tumor necrosis factor (TNF)-alpha failed to alter adherence-induced steady-state IL-8 mRNA levels. Cycloheximide 253-266 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 1912761-2 1991 During 12 h following a dose of SR-NaF, serum fluoride levels could be largely kept within the therapeutic window (believed to be 95-190 ng/ml or 5-10 mumol/l). Fluorides 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 35-38 1715699-0 1991 Interleukin 8-inhibitor and inducer of histamine and leukotriene release in human basophils. Histamine 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1715699-0 1991 Interleukin 8-inhibitor and inducer of histamine and leukotriene release in human basophils. Leukotrienes 53-64 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 1715699-1 1991 We have shown previously that interleukin 8 (IL-8) induces histamine and leukotriene release in human basophils exposed to interleukin 3 (IL-3). Histamine 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 1715699-1 1991 We have shown previously that interleukin 8 (IL-8) induces histamine and leukotriene release in human basophils exposed to interleukin 3 (IL-3). Histamine 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 1715699-1 1991 We have shown previously that interleukin 8 (IL-8) induces histamine and leukotriene release in human basophils exposed to interleukin 3 (IL-3). Leukotrienes 73-84 C-X-C motif chemokine ligand 8 Homo sapiens 30-43 1715699-1 1991 We have shown previously that interleukin 8 (IL-8) induces histamine and leukotriene release in human basophils exposed to interleukin 3 (IL-3). Leukotrienes 73-84 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 1651933-12 1991 The tyrosine phosphatase was inhibited by ammonium molybdate (IC50 of 2 microM), sodium vanadate (IC50 of 150 microM) and the divalent cations Mg2+, Mn2+, and Ca2+ at millimolar concentrations, but not by 100 microM ZnCl or 10 mM NaF. ammonium molybdate 42-60 C-X-C motif chemokine ligand 8 Homo sapiens 230-233 1651933-12 1991 The tyrosine phosphatase was inhibited by ammonium molybdate (IC50 of 2 microM), sodium vanadate (IC50 of 150 microM) and the divalent cations Mg2+, Mn2+, and Ca2+ at millimolar concentrations, but not by 100 microM ZnCl or 10 mM NaF. Vanadates 81-96 C-X-C motif chemokine ligand 8 Homo sapiens 230-233 1651933-12 1991 The tyrosine phosphatase was inhibited by ammonium molybdate (IC50 of 2 microM), sodium vanadate (IC50 of 150 microM) and the divalent cations Mg2+, Mn2+, and Ca2+ at millimolar concentrations, but not by 100 microM ZnCl or 10 mM NaF. magnesium ion 143-147 C-X-C motif chemokine ligand 8 Homo sapiens 230-233 1651933-12 1991 The tyrosine phosphatase was inhibited by ammonium molybdate (IC50 of 2 microM), sodium vanadate (IC50 of 150 microM) and the divalent cations Mg2+, Mn2+, and Ca2+ at millimolar concentrations, but not by 100 microM ZnCl or 10 mM NaF. Manganese(2+) 149-153 C-X-C motif chemokine ligand 8 Homo sapiens 230-233 1654060-2 1991 We report that sodium fluoride (NaF), a potent activator of cellular guanine nucleotide-binding proteins, affected time- and concentration-dependent generation of prostacyclin (PGI2) by cultured human umbilical vein endothelial cells without evidence of cellular toxicity detected by 51Cr or lactate dehydrogenase release. Sodium Fluoride 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 1654060-2 1991 We report that sodium fluoride (NaF), a potent activator of cellular guanine nucleotide-binding proteins, affected time- and concentration-dependent generation of prostacyclin (PGI2) by cultured human umbilical vein endothelial cells without evidence of cellular toxicity detected by 51Cr or lactate dehydrogenase release. Guanine Nucleotides 69-87 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 1654060-2 1991 We report that sodium fluoride (NaF), a potent activator of cellular guanine nucleotide-binding proteins, affected time- and concentration-dependent generation of prostacyclin (PGI2) by cultured human umbilical vein endothelial cells without evidence of cellular toxicity detected by 51Cr or lactate dehydrogenase release. Epoprostenol 163-175 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 1654060-2 1991 We report that sodium fluoride (NaF), a potent activator of cellular guanine nucleotide-binding proteins, affected time- and concentration-dependent generation of prostacyclin (PGI2) by cultured human umbilical vein endothelial cells without evidence of cellular toxicity detected by 51Cr or lactate dehydrogenase release. Epoprostenol 177-181 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 1654060-3 1991 PGI2 synthesis by NaF-stimulated endothelial cells was associated with increases in arachidonate release, phosphoinositide hydrolysis, generation of inositol phosphates, and accumulation of diacylglycerol. Epoprostenol 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1654060-3 1991 PGI2 synthesis by NaF-stimulated endothelial cells was associated with increases in arachidonate release, phosphoinositide hydrolysis, generation of inositol phosphates, and accumulation of diacylglycerol. Arachidonic Acid 84-96 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1654060-3 1991 PGI2 synthesis by NaF-stimulated endothelial cells was associated with increases in arachidonate release, phosphoinositide hydrolysis, generation of inositol phosphates, and accumulation of diacylglycerol. Phosphatidylinositols 106-122 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1654060-3 1991 PGI2 synthesis by NaF-stimulated endothelial cells was associated with increases in arachidonate release, phosphoinositide hydrolysis, generation of inositol phosphates, and accumulation of diacylglycerol. Inositol Phosphates 149-168 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1654060-3 1991 PGI2 synthesis by NaF-stimulated endothelial cells was associated with increases in arachidonate release, phosphoinositide hydrolysis, generation of inositol phosphates, and accumulation of diacylglycerol. Diglycerides 190-204 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 1912761-4 1991 Compared to SR-NaF, IR-NaF caused a significantly higher peak fluoride concentration in serum (322 vs. 158 ng/ml), and greater area under the curve (2269 vs. 1321 ng.h/ml) and urinary fluoride (6.72 vs. 3.80 mg/12 h). Fluorides 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 1912761-4 1991 Compared to SR-NaF, IR-NaF caused a significantly higher peak fluoride concentration in serum (322 vs. 158 ng/ml), and greater area under the curve (2269 vs. 1321 ng.h/ml) and urinary fluoride (6.72 vs. 3.80 mg/12 h). Fluorides 184-192 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 1912761-5 1991 Thus, fluoride absorption from IR-NaF was twice as high as that from SR-NaF. Fluorides 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 34-37 1912761-5 1991 Thus, fluoride absorption from IR-NaF was twice as high as that from SR-NaF. Strontium 69-71 C-X-C motif chemokine ligand 8 Homo sapiens 72-75 1650387-10 1991 Intravenous administration of [Ser-IL-8]72 yielded similar results. Serine 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 1650387-13 1991 Intradermal injections of [Ala-IL-8]77 or [Ser-IL-8]72 induced dose-dependent PMN accumulation, which also was significantly reduced by i.v. Alanine 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 1650387-13 1991 Intradermal injections of [Ala-IL-8]77 or [Ser-IL-8]72 induced dose-dependent PMN accumulation, which also was significantly reduced by i.v. Serine 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 1856209-2 1991 The production of IL-8 is usually not constitutive and can be induced rapidly and abundantly in different cell types by a variety of stimuli such as lipopolysaccharide, interleukin-1, tumor necrosis factor-alpha as well as a tumor promotor phorbol myristate acetate. Tetradecanoylphorbol Acetate 240-265 C-X-C motif chemokine ligand 8 Homo sapiens 18-22 2059236-3 1991 Because the release of monocyte-derived neutrophil chemotactic activity was markedly diminished by pretreatment of the monocytes with cycloheximide, and was completely removed from conditioned media by adsorption to heparin-agarose, we addressed the possibility that monocyte-derived neutrophil chemotactic factor/interleukin-8 (IL-8), a heparin-binding neutrophil-activating polypeptide, might modulate these activities. Heparin 216-223 C-X-C motif chemokine ligand 8 Homo sapiens 329-333 2059236-5 1991 In addition, an IL-8-specific antibody markedly inhibited the neutrophil-activating capacity of the conditioned media from monocytes activated by urate crystals, as well as by inflammatory silica crystals. Uric Acid 146-151 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 2059236-5 1991 In addition, an IL-8-specific antibody markedly inhibited the neutrophil-activating capacity of the conditioned media from monocytes activated by urate crystals, as well as by inflammatory silica crystals. Silicon Dioxide 189-195 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 1882646-0 1991 Release of fluoride and metal ions from root surfaces after topical application of TiF4, SnF2, and NaF in vitro. Fluorides 11-19 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 1937585-3 1991 The buffy-coat cellular expression of neutrophil chemotactic/activating factor/interleukin 8 (IL-8) and monocyte chemotactic/activating protein (MCP-1) mRNA were time and dose-dependent in response to either lipopolysaccharide or zymosan stimulation. Zymosan 230-237 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 1921160-2 1991 Dexamethasone treatment of mesangial cells induced partial inhibition of the release of extracellular IL-8, while cell-associated IL-8 and IL-8 mRNA were not significantly altered. Dexamethasone 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 2037605-10 1991 Stimulation of neutrophils with NAP-1/IL-8 resulted in desensitization toward a subsequent challenge with NAP-2 or gro/MGSA as shown by the rise in cytosolic free calcium. Calcium 163-170 C-X-C motif chemokine ligand 8 Homo sapiens 32-37 2037605-10 1991 Stimulation of neutrophils with NAP-1/IL-8 resulted in desensitization toward a subsequent challenge with NAP-2 or gro/MGSA as shown by the rise in cytosolic free calcium. Calcium 163-170 C-X-C motif chemokine ligand 8 Homo sapiens 38-42 1873480-5 1991 Therefore, we addressed the question of whether the clinical improvement of psoriatic patients during CsA therapy may be due to an inhibition of NAP-1/IL-8 production and secretion from monocytes. Cyclosporine 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 145-150 1873480-5 1991 Therefore, we addressed the question of whether the clinical improvement of psoriatic patients during CsA therapy may be due to an inhibition of NAP-1/IL-8 production and secretion from monocytes. Cyclosporine 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 1652553-6 1991 Neither chemiluminescence by PMN nor platelet aggregation showed a similar pattern compared to the mediator release: PMN preincubated with FMLP followed by NaF resulted in a second chemiluminescence response; the aggregation of platelets which were preincubated with thrombin was partially inhibited by the addition of NaF. platensimycin 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 319-322 1882646-0 1991 Release of fluoride and metal ions from root surfaces after topical application of TiF4, SnF2, and NaF in vitro. Metals 24-29 C-X-C motif chemokine ligand 8 Homo sapiens 99-102 1827816-3 1991 However T cells stimulated with a combination of PMA and ionomycin or PMA and PHA expressed IL-8 mRNA in a PMA dose-dependent manner and maximally after 3 to 6 h of culture. Ionomycin 57-66 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 1827816-6 1991 In addition, immunoprecipitation analysis of PMA/ionomycin-treated T cell lysates detected only minor levels of cellular IL-8 Ag thereby suggesting that in T cells, the production of IL-8 was inhibited at the posttranscriptional level. Tetradecanoylphorbol Acetate 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 1827816-6 1991 In addition, immunoprecipitation analysis of PMA/ionomycin-treated T cell lysates detected only minor levels of cellular IL-8 Ag thereby suggesting that in T cells, the production of IL-8 was inhibited at the posttranscriptional level. Ionomycin 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 1827816-6 1991 In addition, immunoprecipitation analysis of PMA/ionomycin-treated T cell lysates detected only minor levels of cellular IL-8 Ag thereby suggesting that in T cells, the production of IL-8 was inhibited at the posttranscriptional level. Ionomycin 49-58 C-X-C motif chemokine ligand 8 Homo sapiens 183-187 1851210-3 1991 Ethanol exposure reduced guanosine 5"-O-(3-thiotriphosphate) [GTP(S)]- and, to a lesser extent, NaF/AlCl3-stimulated phosphoinositide hydrolysis, whereas it had no effect on the enzymatic activity of a phosphatidylinositol 4,5-bisphosphate-specific phospholipase C. [3H]Bradykinin binding in the absence of GTP(S) was not influenced by ethanol exposure. Ethanol 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 1851210-3 1991 Ethanol exposure reduced guanosine 5"-O-(3-thiotriphosphate) [GTP(S)]- and, to a lesser extent, NaF/AlCl3-stimulated phosphoinositide hydrolysis, whereas it had no effect on the enzymatic activity of a phosphatidylinositol 4,5-bisphosphate-specific phospholipase C. [3H]Bradykinin binding in the absence of GTP(S) was not influenced by ethanol exposure. Aluminum Chloride 100-105 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 1851210-3 1991 Ethanol exposure reduced guanosine 5"-O-(3-thiotriphosphate) [GTP(S)]- and, to a lesser extent, NaF/AlCl3-stimulated phosphoinositide hydrolysis, whereas it had no effect on the enzymatic activity of a phosphatidylinositol 4,5-bisphosphate-specific phospholipase C. [3H]Bradykinin binding in the absence of GTP(S) was not influenced by ethanol exposure. Phosphatidylinositols 117-133 C-X-C motif chemokine ligand 8 Homo sapiens 96-99 1945816-8 1991 The slabs treated with 2% NaF and then 1 mol/L KOH would contain the KOH-insoluble fluoride. potassium hydroxide 69-72 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 1945816-8 1991 The slabs treated with 2% NaF and then 1 mol/L KOH would contain the KOH-insoluble fluoride. Fluorides 83-91 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 1945816-9 1991 Those treated with only 2% NaF would, in addition, contain KOH-soluble fluoride. potassium hydroxide 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 1945816-9 1991 Those treated with only 2% NaF would, in addition, contain KOH-soluble fluoride. Fluorides 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 2007851-6 1991 IL-8 levels peaked at 2 h in subjects given either endotoxin alone or endotoxin/pentoxifylline, falling towards baseline by 5 h. Subjects given endotoxin/ibuprofen had a more sustained rise in IL-8 with peak levels 2.8- and 2.5-fold higher at 3 h compared to endotoxin alone (p = 0.048) or endotoxin/pentoxifylline (p = 0.023), respectively. Pentoxifylline 300-314 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 1802021-2 1991 However, tetraplatin was a much more potent inhibitor than cisplatin, with its I50 values being 1/25, 1/45, and 1/130 that of cisplatin in the presence of DA/Gpp(NH)p, NaF/AlCl3, and forskolin/Gpp(NH)p respectively. ormaplatin 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 1802021-2 1991 However, tetraplatin was a much more potent inhibitor than cisplatin, with its I50 values being 1/25, 1/45, and 1/130 that of cisplatin in the presence of DA/Gpp(NH)p, NaF/AlCl3, and forskolin/Gpp(NH)p respectively. Cisplatin 59-68 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 1802021-2 1991 However, tetraplatin was a much more potent inhibitor than cisplatin, with its I50 values being 1/25, 1/45, and 1/130 that of cisplatin in the presence of DA/Gpp(NH)p, NaF/AlCl3, and forskolin/Gpp(NH)p respectively. Cisplatin 126-135 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 1802021-2 1991 However, tetraplatin was a much more potent inhibitor than cisplatin, with its I50 values being 1/25, 1/45, and 1/130 that of cisplatin in the presence of DA/Gpp(NH)p, NaF/AlCl3, and forskolin/Gpp(NH)p respectively. Phosphorus 14-15 C-X-C motif chemokine ligand 8 Homo sapiens 168-171 1680309-7 1991 Higher concentrations of BeSO4 precipitated tubulin, an effect which was not affected by Mg2+, partially prevented but not reversed by MAPs, and prevented or reversed by either NaF or nucleotides at adequate concentrations. beryllium sulfate 25-30 C-X-C motif chemokine ligand 8 Homo sapiens 177-180 2007851-6 1991 IL-8 levels peaked at 2 h in subjects given either endotoxin alone or endotoxin/pentoxifylline, falling towards baseline by 5 h. Subjects given endotoxin/ibuprofen had a more sustained rise in IL-8 with peak levels 2.8- and 2.5-fold higher at 3 h compared to endotoxin alone (p = 0.048) or endotoxin/pentoxifylline (p = 0.023), respectively. Pentoxifylline 80-94 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 2007851-6 1991 IL-8 levels peaked at 2 h in subjects given either endotoxin alone or endotoxin/pentoxifylline, falling towards baseline by 5 h. Subjects given endotoxin/ibuprofen had a more sustained rise in IL-8 with peak levels 2.8- and 2.5-fold higher at 3 h compared to endotoxin alone (p = 0.048) or endotoxin/pentoxifylline (p = 0.023), respectively. Ibuprofen 154-163 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 2007851-6 1991 IL-8 levels peaked at 2 h in subjects given either endotoxin alone or endotoxin/pentoxifylline, falling towards baseline by 5 h. Subjects given endotoxin/ibuprofen had a more sustained rise in IL-8 with peak levels 2.8- and 2.5-fold higher at 3 h compared to endotoxin alone (p = 0.048) or endotoxin/pentoxifylline (p = 0.023), respectively. Ibuprofen 154-163 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 1674864-3 1991 On the other hand, pretreatment of MKN-45 cells with retinoic acid (RA) significantly enhanced histamine-induced increase of cyclic AMP production, although the cyclic AMP response to either forskolin or NaF was not affected. Tretinoin 68-70 C-X-C motif chemokine ligand 8 Homo sapiens 204-207 1674864-3 1991 On the other hand, pretreatment of MKN-45 cells with retinoic acid (RA) significantly enhanced histamine-induced increase of cyclic AMP production, although the cyclic AMP response to either forskolin or NaF was not affected. Cyclic AMP 161-171 C-X-C motif chemokine ligand 8 Homo sapiens 204-207 2039486-0 1991 1,25(OH)2-D3 is a potent regulator of interleukin-1 induced interleukin-8 expression and production. Calcitriol 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 60-73 2039486-3 1991 We studied the possible effect of an endogenous immune modulator 1,25(OH)2-cholecalciferol (1,25(OH)2-D3) on the IL-1-induced IL-8-production by several types of cells. 1,25(oh)2-cholecalciferol 65-90 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 2039486-3 1991 We studied the possible effect of an endogenous immune modulator 1,25(OH)2-cholecalciferol (1,25(OH)2-D3) on the IL-1-induced IL-8-production by several types of cells. Calcitriol 92-104 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 2039486-4 1991 1,25(OH)2-D3 inhibited the IL-1-alpha induced IL-8 production and mRNA expression in keratinocytes, fibroblasts and PBMC, but not in endothelial cells. Calcitriol 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Arginine 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Arginine 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Leucine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Leucine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Leucine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Leucine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Leucine 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Arginine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 65-78 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Arginine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Arginine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Arginine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1828038-1 1991 Plasmin mainly cleaved the Arg5-Ser6 bond of Arg-Val-Leu-Pro-Arg-interleukin-8 (AVLPR-IL-8) produced by human dermal fibroblasts, which resulted in the conversion of AVLPR-IL-8 to IL-8 and the inactive pentapeptide, though a minor cleavage of AVLPR-IL-8 by plasmin at Lys8-Glu9 bond occurred. Arginine 45-48 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 1893074-4 1991 Southern blot analyses of plasmids containing IL-1 beta and IL-8 gave positive results with the 3" degenerate probe, 5"-acr-dTATTTATTN, clearly showing that the very short probe approach can be used in this type of analysis. 5"-acr-dtatttattn 117-134 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 2045129-0 1991 Interleukin-3, interleukin-8, FMLP and C5a enhance the release of leukotrienes from neutrophils of patients with atopic dermatitis. Leukotrienes 66-78 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 1878329-2 1991 In the test group (n = 123, biweekly mouthrinsing with a 2% solution of mineralizing agent and 0.2% NaF solution) the percentage reduction in increment of both EFDS and DFS was high, whereas in the control group (n = 123, biweekly mouthrinsing with placebo and 0.2% NaF solutions) the incidence for symptoms of caries disease did not differ from that normally found in this age cohort. aspartyl-phenylalanine 169-172 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 2007851-6 1991 IL-8 levels peaked at 2 h in subjects given either endotoxin alone or endotoxin/pentoxifylline, falling towards baseline by 5 h. Subjects given endotoxin/ibuprofen had a more sustained rise in IL-8 with peak levels 2.8- and 2.5-fold higher at 3 h compared to endotoxin alone (p = 0.048) or endotoxin/pentoxifylline (p = 0.023), respectively. Pentoxifylline 300-314 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 2007851-8 1991 This trend reflected the increased release of IL-8 by the subjects receiving ibuprofen compared to pentoxifylline (1.9-fold higher; p = 0.024). Ibuprofen 77-86 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 1850243-5 1991 However, propranolol induced a similar dose-dependent inhibition of O2- generation in neutrophils stimulated with either FMLP + cytochalasin B or with 20.0 mM NaF. Propranolol 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 159-162 1873359-8 1991 An eventual decrease in the recovery of rTNF after collection of blood was prevented in the oxalate/NaF tubes. Oxalates 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 2007144-5 1991 Synthetic and recombinant NAP-1/IL-8 were equally active on human neutrophil granulocytes as determined by measuring the induction of cytosolic free calcium, elastase release, and chemotaxis. Calcium 149-156 C-X-C motif chemokine ligand 8 Homo sapiens 26-31 2007144-5 1991 Synthetic and recombinant NAP-1/IL-8 were equally active on human neutrophil granulocytes as determined by measuring the induction of cytosolic free calcium, elastase release, and chemotaxis. Calcium 149-156 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 1850243-1 1991 Relatively high levels of propranolol (170 microM) markedly attenuated the generation of 1,2 diacylglycerol in neutrophils stimulated with either FMLP plus cytochalasin B or with 20.0 mM NaF. Propranolol 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 187-190 1850243-1 1991 Relatively high levels of propranolol (170 microM) markedly attenuated the generation of 1,2 diacylglycerol in neutrophils stimulated with either FMLP plus cytochalasin B or with 20.0 mM NaF. 1,2-diacylglycerol 89-107 C-X-C motif chemokine ligand 8 Homo sapiens 187-190 2055605-6 1991 The assay was able to detect IL-8 when the samples were prepared in either normal saline, RPMI, or human plasma. rpmi 90-94 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 1899427-10 1991 The production of NAP-1/IL-8 was markedly reduced by dexamethasone in phagocytosis-stimulated PBMC, and almost totally inhibited in SFMC obtained from joints after intraarticular administration of betamethasone. Dexamethasone 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 1899427-10 1991 The production of NAP-1/IL-8 was markedly reduced by dexamethasone in phagocytosis-stimulated PBMC, and almost totally inhibited in SFMC obtained from joints after intraarticular administration of betamethasone. Betamethasone 197-210 C-X-C motif chemokine ligand 8 Homo sapiens 18-23 1899427-10 1991 The production of NAP-1/IL-8 was markedly reduced by dexamethasone in phagocytosis-stimulated PBMC, and almost totally inhibited in SFMC obtained from joints after intraarticular administration of betamethasone. Betamethasone 197-210 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 1899427-11 1991 By contrast, the cyclooxygenase inhibitor, indomethacin, tended to increase the NAP-1/IL-8 yield from PBMC in culture. Indomethacin 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 1899427-11 1991 By contrast, the cyclooxygenase inhibitor, indomethacin, tended to increase the NAP-1/IL-8 yield from PBMC in culture. Indomethacin 43-55 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 1846901-0 1991 Recombinant human interleukin-8 is a potent activator of canine neutrophil aggregation, migration, and leukotriene B4 biosynthesis. Leukotriene B4 103-117 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 1848431-4 1991 In this study, we cocultured neutrophils with 35S-sulfate-labeled cartilage and found that the addition of recombinant human IL-8 (rHuIL-8) caused rapid, neutrophil-mediated cartilage degradation that was the result of induction of neutrophil degranulation by the cytokine. 35s-sulfate 46-57 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 1901832-4 1991 The combined incubation of platelets with PCB and sodium fluoride (NaF), an activator of G-proteins, resulted in synergistic 12-HETE generation compared to stimulation with NaF or PCB alone. Polychlorinated Biphenyls 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 1901832-4 1991 The combined incubation of platelets with PCB and sodium fluoride (NaF), an activator of G-proteins, resulted in synergistic 12-HETE generation compared to stimulation with NaF or PCB alone. Polychlorinated Biphenyls 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 173-176 1901832-4 1991 The combined incubation of platelets with PCB and sodium fluoride (NaF), an activator of G-proteins, resulted in synergistic 12-HETE generation compared to stimulation with NaF or PCB alone. Sodium Fluoride 50-65 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 1901832-4 1991 The combined incubation of platelets with PCB and sodium fluoride (NaF), an activator of G-proteins, resulted in synergistic 12-HETE generation compared to stimulation with NaF or PCB alone. Sodium Fluoride 50-65 C-X-C motif chemokine ligand 8 Homo sapiens 173-176 1901832-4 1991 The combined incubation of platelets with PCB and sodium fluoride (NaF), an activator of G-proteins, resulted in synergistic 12-HETE generation compared to stimulation with NaF or PCB alone. 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid 125-132 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 1901832-4 1991 The combined incubation of platelets with PCB and sodium fluoride (NaF), an activator of G-proteins, resulted in synergistic 12-HETE generation compared to stimulation with NaF or PCB alone. Polychlorinated Biphenyls 180-183 C-X-C motif chemokine ligand 8 Homo sapiens 67-70 1899427-7 1991 In addition to LPS, rheumatoid factor-containing immune complexes, zymosan, and IL-1 were highly effective in inducing NAP-1/IL-8 production, while IL-3, GM-CSF, tumor necrosis factor (TNF), and IL-2 were somewhat less potent. Zymosan 67-74 C-X-C motif chemokine ligand 8 Homo sapiens 119-124 1899427-7 1991 In addition to LPS, rheumatoid factor-containing immune complexes, zymosan, and IL-1 were highly effective in inducing NAP-1/IL-8 production, while IL-3, GM-CSF, tumor necrosis factor (TNF), and IL-2 were somewhat less potent. Zymosan 67-74 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 1899427-10 1991 The production of NAP-1/IL-8 was markedly reduced by dexamethasone in phagocytosis-stimulated PBMC, and almost totally inhibited in SFMC obtained from joints after intraarticular administration of betamethasone. Dexamethasone 53-66 C-X-C motif chemokine ligand 8 Homo sapiens 18-23 1790390-1 1991 Fifty-two postmenopausal women (mean age 60 +/- 5 years) with low BMD (less than -2SD of young adult values) but who had not experienced previous crush fracture were treated with 50 mg of sodium fluoride (NaF), 1 g of calcium and 400 IU of vitamin D2 per day for 2 years. Sodium Fluoride 188-203 C-X-C motif chemokine ligand 8 Homo sapiens 205-208 1703410-6 1991 O2- formation stimulated by complement C5a, concanavalin A, NaF, A 23187, phorbol myristate acetate and arachidonic acid was not affected by Bt2cCMP. Superoxides 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 1903636-5 1991 Retinoic acid treatment, in a time- and concentration-dependent manner, led to a decrease in phospholipase C activity when stimulated with either GTP gamma S or NaF, both of which activate the enzyme via the G-protein. Tretinoin 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 161-164 2070378-4 1991 NaF treatment resulted in mean fluoride concentrations of 7,818 ppm. Fluorides 31-39 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2176614-3 1990 In the presence of poly(dT).r(pA)10 template.primer complex and NaF, we observed AMP, ADP, ATP, PPi and dATP to be competitive inhibitors of the FK-catalyzed DNA polymerization. Adenosine Monophosphate 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 1752702-2 1991 Exposure of human peripheral blood monocytes to MPG in vitro induced high levels of mRNA transcripts for IL-8 and MCP, as assessed by Northern blot analysis. (9H-purin-6-yl)thiomethyl glutamate 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 1812910-9 1991 In contrast to the latter effects, a dual-active NaF+MFP dentifrice in a calcium abrasive system exhibited decreased efficacy relative to a silica abrasive formulation due to incompatibility of free fluoride ion. Calcium 73-80 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 1812910-9 1991 In contrast to the latter effects, a dual-active NaF+MFP dentifrice in a calcium abrasive system exhibited decreased efficacy relative to a silica abrasive formulation due to incompatibility of free fluoride ion. Fluorides 199-207 C-X-C motif chemokine ligand 8 Homo sapiens 49-52 1937907-1 1991 Simultaneous stimulation of human neutrophils (PMN) with the receptor-mediated activator formyl-met-leu-phe (FMLP) and the G protein activator sodium fluoride (NaF) resulted in the synergistic generation of leukotrienes. N-Formylmethionine Leucyl-Phenylalanine 89-107 C-X-C motif chemokine ligand 8 Homo sapiens 160-163 1937907-1 1991 Simultaneous stimulation of human neutrophils (PMN) with the receptor-mediated activator formyl-met-leu-phe (FMLP) and the G protein activator sodium fluoride (NaF) resulted in the synergistic generation of leukotrienes. Sodium Fluoride 143-158 C-X-C motif chemokine ligand 8 Homo sapiens 160-163 1937907-1 1991 Simultaneous stimulation of human neutrophils (PMN) with the receptor-mediated activator formyl-met-leu-phe (FMLP) and the G protein activator sodium fluoride (NaF) resulted in the synergistic generation of leukotrienes. Leukotrienes 207-219 C-X-C motif chemokine ligand 8 Homo sapiens 160-163 1937907-2 1991 Activation of human platelets with thrombin and NaF showed an additive formation of 12-HETE. 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid 84-91 C-X-C motif chemokine ligand 8 Homo sapiens 48-51 27467661-4 1991 Included among these is a distinct isoenzyme (group), defined by IEF with acidic isoelectric points (pI) of approximately 6.0, that is characterized by its strong staining intensity and inhibition by sodium fluoride (NaF). Sodium Fluoride 200-215 C-X-C motif chemokine ligand 8 Homo sapiens 217-220 2176614-3 1990 In the presence of poly(dT).r(pA)10 template.primer complex and NaF, we observed AMP, ADP, ATP, PPi and dATP to be competitive inhibitors of the FK-catalyzed DNA polymerization. Adenosine Diphosphate 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 2176614-3 1990 In the presence of poly(dT).r(pA)10 template.primer complex and NaF, we observed AMP, ADP, ATP, PPi and dATP to be competitive inhibitors of the FK-catalyzed DNA polymerization. Adenosine Triphosphate 91-94 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 2176614-3 1990 In the presence of poly(dT).r(pA)10 template.primer complex and NaF, we observed AMP, ADP, ATP, PPi and dATP to be competitive inhibitors of the FK-catalyzed DNA polymerization. 2'-deoxyadenosine triphosphate 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 2097295-0 1990 Effect of exogenous prostaglandin E2 and actinomycin D on plasma leakage induced by neutrophil-activating peptide-1/interleukin-8. Dinoprostone 20-36 C-X-C motif chemokine ligand 8 Homo sapiens 84-115 2097295-0 1990 Effect of exogenous prostaglandin E2 and actinomycin D on plasma leakage induced by neutrophil-activating peptide-1/interleukin-8. Dinoprostone 20-36 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 2097295-0 1990 Effect of exogenous prostaglandin E2 and actinomycin D on plasma leakage induced by neutrophil-activating peptide-1/interleukin-8. Dactinomycin 41-54 C-X-C motif chemokine ligand 8 Homo sapiens 84-115 2097295-0 1990 Effect of exogenous prostaglandin E2 and actinomycin D on plasma leakage induced by neutrophil-activating peptide-1/interleukin-8. Dactinomycin 41-54 C-X-C motif chemokine ligand 8 Homo sapiens 116-129 2097295-3 1990 Co-injection of prostaglandin E2 (PGE2) extended the threshold of inflammatory activity of NAP-1/IL-8 to less than 10(-13) moles/site and caused approximately three-fold increases in neutrophil accumulation and ten-fold increases in plasma leakage at the higher doses of NAP-1/IL-8 examined. Dinoprostone 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 91-96 2097295-3 1990 Co-injection of prostaglandin E2 (PGE2) extended the threshold of inflammatory activity of NAP-1/IL-8 to less than 10(-13) moles/site and caused approximately three-fold increases in neutrophil accumulation and ten-fold increases in plasma leakage at the higher doses of NAP-1/IL-8 examined. Dinoprostone 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 2097295-3 1990 Co-injection of prostaglandin E2 (PGE2) extended the threshold of inflammatory activity of NAP-1/IL-8 to less than 10(-13) moles/site and caused approximately three-fold increases in neutrophil accumulation and ten-fold increases in plasma leakage at the higher doses of NAP-1/IL-8 examined. Dinoprostone 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 271-276 2126013-6 1990 Similar results were obtained when ATP was depleted by incubation of cells either under a N2-atmosphere or in the presence of NaN3 and NaF. Adenosine Triphosphate 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 135-138 2097295-3 1990 Co-injection of prostaglandin E2 (PGE2) extended the threshold of inflammatory activity of NAP-1/IL-8 to less than 10(-13) moles/site and caused approximately three-fold increases in neutrophil accumulation and ten-fold increases in plasma leakage at the higher doses of NAP-1/IL-8 examined. Dinoprostone 16-32 C-X-C motif chemokine ligand 8 Homo sapiens 277-281 2097295-3 1990 Co-injection of prostaglandin E2 (PGE2) extended the threshold of inflammatory activity of NAP-1/IL-8 to less than 10(-13) moles/site and caused approximately three-fold increases in neutrophil accumulation and ten-fold increases in plasma leakage at the higher doses of NAP-1/IL-8 examined. Dinoprostone 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 91-96 2097295-3 1990 Co-injection of prostaglandin E2 (PGE2) extended the threshold of inflammatory activity of NAP-1/IL-8 to less than 10(-13) moles/site and caused approximately three-fold increases in neutrophil accumulation and ten-fold increases in plasma leakage at the higher doses of NAP-1/IL-8 examined. Dinoprostone 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 2097295-3 1990 Co-injection of prostaglandin E2 (PGE2) extended the threshold of inflammatory activity of NAP-1/IL-8 to less than 10(-13) moles/site and caused approximately three-fold increases in neutrophil accumulation and ten-fold increases in plasma leakage at the higher doses of NAP-1/IL-8 examined. Dinoprostone 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 271-276 2097295-3 1990 Co-injection of prostaglandin E2 (PGE2) extended the threshold of inflammatory activity of NAP-1/IL-8 to less than 10(-13) moles/site and caused approximately three-fold increases in neutrophil accumulation and ten-fold increases in plasma leakage at the higher doses of NAP-1/IL-8 examined. Dinoprostone 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 277-281 2173722-5 1990 Release of NAP-1 was stimulus specific because A23187 evoked the release of LTB4 but not NAP-1, whereas LPS and zymosan induced the release of both LTB4 and NAP-1. Calcimycin 47-53 C-X-C motif chemokine ligand 8 Homo sapiens 11-16 2170531-5 1990 Pretreatment of neutrophils with either GM-CSF or TNF-alpha dose-dependently enhanced the production of superoxide induced by NaF, as determined by the superoxide dismutase-inhibitable reduction of ferricytochrome c. Superoxides 104-114 C-X-C motif chemokine ligand 8 Homo sapiens 126-129 2173722-0 1990 Macrophages cultured in vitro release leukotriene B4 and neutrophil attractant/activation protein (interleukin 8) sequentially in response to stimulation with lipopolysaccharide and zymosan. Zymosan 182-189 C-X-C motif chemokine ligand 8 Homo sapiens 99-112 2173722-1 1990 The capacity of lipopolysaccharide (LPS), zymosan, and calcium ionophore A23187 to induce neutrophil chemotactic activity (NCA), leukotriene B4 (LTB4), and neutrophil attractant/activation protein (NAP-1) release from human alveolar macrophages (AM) retrieved from normal nonsmokers was evaluated. Calcimycin 73-79 C-X-C motif chemokine ligand 8 Homo sapiens 198-203 2173722-5 1990 Release of NAP-1 was stimulus specific because A23187 evoked the release of LTB4 but not NAP-1, whereas LPS and zymosan induced the release of both LTB4 and NAP-1. Zymosan 112-119 C-X-C motif chemokine ligand 8 Homo sapiens 11-16 2173722-8 1990 Preincubation of AM with nordihydroguiaretic acid (10(-4) M) completely abolished the appearance of NCA, LTB4, and NAP-1 in supernatants of AM challenged with LPS. Masoprocol 25-49 C-X-C motif chemokine ligand 8 Homo sapiens 115-120 2173722-9 1990 Therefore, LPS and zymosan particles were potent stimuli of the sequential release of LTB4 and NAP-1 from AM. Zymosan 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 2170531-5 1990 Pretreatment of neutrophils with either GM-CSF or TNF-alpha dose-dependently enhanced the production of superoxide induced by NaF, as determined by the superoxide dismutase-inhibitable reduction of ferricytochrome c. Carbon 82-83 C-X-C motif chemokine ligand 8 Homo sapiens 126-129 2212672-4 1990 The IL-8 isolated from each of these cell types is a mixture of two IL-8 polypeptides, one consisting of 72 amino acids (herein called [ser-IL-8]72) and the other 77 amino acids (an N-terminal extended form herein called [ala-IL-8]77). Serine 136-139 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 2212672-4 1990 The IL-8 isolated from each of these cell types is a mixture of two IL-8 polypeptides, one consisting of 72 amino acids (herein called [ser-IL-8]72) and the other 77 amino acids (an N-terminal extended form herein called [ala-IL-8]77). Alanine 222-225 C-X-C motif chemokine ligand 8 Homo sapiens 4-8 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Cytochalasin B 45-59 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 2096385-1 1990 Cytotoxicity of sodium fluoride (NaF) on human diploid cells in exponential growth was investigated using a) Flow 1000 cells, passage No. Sodium Fluoride 16-31 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Serine 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Serine 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Serine 82-85 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Alanine 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Alanine 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Alanine 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 2212672-13 1990 Our data suggest that [ala-IL-8]77 and [ser-IL-8]72 have qualitatively similar and potentially complex biological activities, and that full activation of IL-8 requires cleavage to the [ser-IL-8]72 form. Alanine 23-26 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 2212672-13 1990 Our data suggest that [ala-IL-8]77 and [ser-IL-8]72 have qualitatively similar and potentially complex biological activities, and that full activation of IL-8 requires cleavage to the [ser-IL-8]72 form. Serine 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 2212672-13 1990 Our data suggest that [ala-IL-8]77 and [ser-IL-8]72 have qualitatively similar and potentially complex biological activities, and that full activation of IL-8 requires cleavage to the [ser-IL-8]72 form. Serine 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 2212672-13 1990 Our data suggest that [ala-IL-8]77 and [ser-IL-8]72 have qualitatively similar and potentially complex biological activities, and that full activation of IL-8 requires cleavage to the [ser-IL-8]72 form. Serine 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 2212672-13 1990 Our data suggest that [ala-IL-8]77 and [ser-IL-8]72 have qualitatively similar and potentially complex biological activities, and that full activation of IL-8 requires cleavage to the [ser-IL-8]72 form. Serine 185-188 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 2212672-5 1990 IL-8 derived from T lymphocytes and monocytes is predominantly [ser-IL-8]72, whereas endothelial-derived IL-8 is highly enriched (greater than 80%) in [ala-IL-8]77. Serine 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 2212672-5 1990 IL-8 derived from T lymphocytes and monocytes is predominantly [ser-IL-8]72, whereas endothelial-derived IL-8 is highly enriched (greater than 80%) in [ala-IL-8]77. Serine 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 2212672-5 1990 IL-8 derived from T lymphocytes and monocytes is predominantly [ser-IL-8]72, whereas endothelial-derived IL-8 is highly enriched (greater than 80%) in [ala-IL-8]77. Serine 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 2212672-5 1990 IL-8 derived from T lymphocytes and monocytes is predominantly [ser-IL-8]72, whereas endothelial-derived IL-8 is highly enriched (greater than 80%) in [ala-IL-8]77. Serine 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 2212672-7 1990 Thrombin was found to efficiently convert [ala-IL-8]77 to [ser-IL-8]72. Alanine 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 2212672-7 1990 Thrombin was found to efficiently convert [ala-IL-8]77 to [ser-IL-8]72. Alanine 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 2212672-7 1990 Thrombin was found to efficiently convert [ala-IL-8]77 to [ser-IL-8]72. Serine 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 2212672-7 1990 Thrombin was found to efficiently convert [ala-IL-8]77 to [ser-IL-8]72. Serine 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 2212672-9 1990 In competitive binding assays using 125I[ala-IL-8]77 neutrophils exhibited a twofold preference for [ser-IL-8]72 over [ala-IL-8]77. Alanine 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 2212672-9 1990 In competitive binding assays using 125I[ala-IL-8]77 neutrophils exhibited a twofold preference for [ser-IL-8]72 over [ala-IL-8]77. Alanine 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 2212672-9 1990 In competitive binding assays using 125I[ala-IL-8]77 neutrophils exhibited a twofold preference for [ser-IL-8]72 over [ala-IL-8]77. Alanine 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 2212672-9 1990 In competitive binding assays using 125I[ala-IL-8]77 neutrophils exhibited a twofold preference for [ser-IL-8]72 over [ala-IL-8]77. Serine 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 2212672-9 1990 In competitive binding assays using 125I[ala-IL-8]77 neutrophils exhibited a twofold preference for [ser-IL-8]72 over [ala-IL-8]77. Serine 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 2212672-9 1990 In competitive binding assays using 125I[ala-IL-8]77 neutrophils exhibited a twofold preference for [ser-IL-8]72 over [ala-IL-8]77. Serine 101-104 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 2212672-11 1990 However, [ser-IL-8]72 was approximately 10-fold more potent than [ala-IL-8]77 in these assays (ED50 approximately 0.3 nM for [ser-IL-8]72 vs approximately 3 nM for [ala-IL-8]77. Serine 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 2212672-11 1990 However, [ser-IL-8]72 was approximately 10-fold more potent than [ala-IL-8]77 in these assays (ED50 approximately 0.3 nM for [ser-IL-8]72 vs approximately 3 nM for [ala-IL-8]77. Alanine 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 2212672-11 1990 However, [ser-IL-8]72 was approximately 10-fold more potent than [ala-IL-8]77 in these assays (ED50 approximately 0.3 nM for [ser-IL-8]72 vs approximately 3 nM for [ala-IL-8]77. Alanine 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 2212672-11 1990 However, [ser-IL-8]72 was approximately 10-fold more potent than [ala-IL-8]77 in these assays (ED50 approximately 0.3 nM for [ser-IL-8]72 vs approximately 3 nM for [ala-IL-8]77. Alanine 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 2212672-11 1990 However, [ser-IL-8]72 was approximately 10-fold more potent than [ala-IL-8]77 in these assays (ED50 approximately 0.3 nM for [ser-IL-8]72 vs approximately 3 nM for [ala-IL-8]77. Serine 126-129 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Cytochalasin B 45-59 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 2212672-12 1990 Both forms of IL-8 promoted degranulation of cytochalasin B-treated neutrophils [[ser-IL-8]72 (ED50 greater than 10 nM) was two- to three-fold more potent than [ala-IL-8]77], although in this regard they were less active than FMLP. Cytochalasin B 45-59 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 1699135-3 1990 Interleukin-8 is a chemoattractant for T cells and neutrophils and is a member of a superfamily of soluble molecules related by a conserved motif containing four cysteine residues. Cysteine 162-170 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 2241978-3 1990 Purification by anti NAP-1/IL-8 affinity chromatography and reversed phase HPLC revealed a single peak showing a single line upon SDS-PAGE corresponding to a Mr of 8000. Sodium Dodecyl Sulfate 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 21-26 2241978-3 1990 Purification by anti NAP-1/IL-8 affinity chromatography and reversed phase HPLC revealed a single peak showing a single line upon SDS-PAGE corresponding to a Mr of 8000. Sodium Dodecyl Sulfate 130-133 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 2136468-6 1990 The combination of calcium, small doses of vitamin D, NaF and exercise used in the treatment of diabetic osteoporoses leads in general to a significant rise of the calcium serum level, an insignificant rise of the phosphorus level and it reduces alkaline phosphatase activity. Calcium 164-171 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 2080951-11 1990 After administration of the products, fluoride appeared in blood with a lag time smaller than 0.05 h and invaded the blood with a t1/2 from 0.07 to 0.12 h. The Cmax of fluoride in plasma was 412-466 ng/ml at a tmax of 0.5-0.7 h. The AUCs of fluoride after Na2FPO3 solution and after Na2FPO3 tablets were within the 0.80-1.20 bioequivalence limits with regard to the AUC after NaF solution. Fluorides 168-176 C-X-C motif chemokine ligand 8 Homo sapiens 376-379 2080951-11 1990 After administration of the products, fluoride appeared in blood with a lag time smaller than 0.05 h and invaded the blood with a t1/2 from 0.07 to 0.12 h. The Cmax of fluoride in plasma was 412-466 ng/ml at a tmax of 0.5-0.7 h. The AUCs of fluoride after Na2FPO3 solution and after Na2FPO3 tablets were within the 0.80-1.20 bioequivalence limits with regard to the AUC after NaF solution. Fluorides 168-176 C-X-C motif chemokine ligand 8 Homo sapiens 376-379 2080951-13 1990 In the 24 h following the administration, the urinary excretion of fluoride accounted for 51 +/- 10%, 46 +/- 6% and 47 +/- 8% of the administered dose, respectively for NaF solution, Na2FPO3 solution and Na2FPO3 + Ca tablets. Fluorides 67-75 C-X-C motif chemokine ligand 8 Homo sapiens 169-172 2200823-7 1990 The IL-4-induced inhibition of IL-8 mRNA expression was dependent on protein synthesis, as the suppressive effects of IL-4 were significantly negated by the addition of cycloheximide. Cycloheximide 169-182 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 2134272-9 1990 The most commonly used fluoride mouth-rinsing solution for daily use is 0.05-0.1% NaF in neutral or weak acid solution. Fluorides 23-31 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 2134272-9 1990 The most commonly used fluoride mouth-rinsing solution for daily use is 0.05-0.1% NaF in neutral or weak acid solution. weak acid 100-109 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 9995899-0 1990 Excited-state absorption by Eu2+ in NaF and KMgF3. europium(2+) 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 2148657-2 1990 NaF (mM) completely inhibits the Ca-ATP-ase activity in presence of 0.02% tween-20. Polysorbates 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2148657-3 1990 The inhibition is time- and NaF-concentration-dependent and increases as affected by AlCl3 (microM). Aluminum Chloride 85-90 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 2148657-4 1990 The potentiated action of AlCl3 depends on the NaF concentration. Aluminum Chloride 26-31 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 2148657-6 1990 NaF inhibits the Ca-ATP-ase competitively with respect to ATP, but NaF plus AlCl3 make the inhibition combined. Adenosine Triphosphate 20-23 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2148657-7 1990 The affinity of the Ca-ATP-ase to the NaF + AlCl3 complex, but not to NaF decreases by 5 mM with an increase of the Pi concentration. Aluminum Chloride 44-49 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 2148657-8 1990 NaF probably interacts with the ATP-binding site and the NaF + AlCl3 complex interacts with the phosphate-binding site of the ATP-ase. Adenosine Triphosphate 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2148657-8 1990 NaF probably interacts with the ATP-binding site and the NaF + AlCl3 complex interacts with the phosphate-binding site of the ATP-ase. Aluminum Chloride 63-68 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 2148657-8 1990 NaF probably interacts with the ATP-binding site and the NaF + AlCl3 complex interacts with the phosphate-binding site of the ATP-ase. Phosphates 96-105 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 2384626-7 1990 The slabs treated with 2% NaF and then with 1 mol/L KOH would contain the KOH-insoluble fluoride. potassium hydroxide 74-77 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 2384626-7 1990 The slabs treated with 2% NaF and then with 1 mol/L KOH would contain the KOH-insoluble fluoride. Fluorides 88-96 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 2384626-8 1990 Those treated with only 2% NaF would, in addition, contain KOH-soluble fluoride. potassium hydroxide 59-62 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 2384626-8 1990 Those treated with only 2% NaF would, in addition, contain KOH-soluble fluoride. Fluorides 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 2168414-3 1990 Although NaF induced the mobilization of Ca2+ from intracellular storage sites in fura2-loaded platelets, it failed to raise pHi as determined from the fluorescence of 2,7-bis-(2-carboxyethyl)-5(6)-carboxyfluorescein-loaded platelets. Fura-2 82-87 C-X-C motif chemokine ligand 8 Homo sapiens 9-12 2168414-4 1990 Furthermore, when thrombin (0.1 unit/ml) or the phorbol ester 12-O-tetradecanoylphorbol 13-acetate (TPA) had raised pHi from 7.13 +/- 0.05 to 7.35 +/- 0.07 (n = 30), addition of NaF (2.5-10 mM) rapidly restored pHi to values found before stimulation. Tetradecanoylphorbol Acetate 100-103 C-X-C motif chemokine ligand 8 Homo sapiens 178-181 2168414-5 1990 Conversely, preincubation of platelets with low concentrations of NaF (2.5 mM) completely prevented alkalinization in response to thrombin or TPA. Tetradecanoylphorbol Acetate 142-145 C-X-C motif chemokine ligand 8 Homo sapiens 66-69 2168414-8 1990 In order to investigate whether the NaF effect was attributable to a G protein, platelets were preincubated with N-ethylmaleimide (50 microM), which is known to inhibit the adenylyl cyclase-inhibitory G protein. Ethylmaleimide 113-129 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 2168414-9 1990 N-Ethylmaleimide treatment not only prevented inhibition of adenylyl cyclase by epinephrine but also completely reversed the inhibitory effect of NaF on the Na+/H+ exchanger. Ethylmaleimide 0-16 C-X-C motif chemokine ligand 8 Homo sapiens 146-149 2384166-1 1990 Activation of transducin-GDP by NaF is mainly mediated by aluminofluorde or beryllofluoride complexes acting as GTP gamma-phosphate analogs. aluminofluorde 58-72 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 2384166-1 1990 Activation of transducin-GDP by NaF is mainly mediated by aluminofluorde or beryllofluoride complexes acting as GTP gamma-phosphate analogs. beryllium fluoride 76-91 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 2136468-6 1990 The combination of calcium, small doses of vitamin D, NaF and exercise used in the treatment of diabetic osteoporoses leads in general to a significant rise of the calcium serum level, an insignificant rise of the phosphorus level and it reduces alkaline phosphatase activity. Phosphorus 214-224 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 2162138-3 1990 Inhibition of isoproterenol-sensitive adenylate cyclase activity could be demonstrated by serum dilutions or IgG in 52% (26 of 50) of the patients; basal and NaF-stimulated activities, in contrast, were unaffected. Isoproterenol 14-27 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 2384166-1 1990 Activation of transducin-GDP by NaF is mainly mediated by aluminofluorde or beryllofluoride complexes acting as GTP gamma-phosphate analogs. gtp gamma-phosphate 112-131 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 2384166-2 1990 In millimolar magnesium, NaF at concentrations above 3 mM is active even in the absence of aluminium or beryllium. Magnesium 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 2384166-2 1990 In millimolar magnesium, NaF at concentrations above 3 mM is active even in the absence of aluminium or beryllium. Aluminum 91-100 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 2384166-2 1990 In millimolar magnesium, NaF at concentrations above 3 mM is active even in the absence of aluminium or beryllium. Beryllium 104-113 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 2384166-5 1990 We propose that at high NaF concentrations, 3 hydrogen-bonded fluorides in the gamma-phosphate site of T alpha GDP entrap a magnesium counterion and this induces the transconformation to the T alpha GTP form. Hydrogen 46-54 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 2384166-5 1990 We propose that at high NaF concentrations, 3 hydrogen-bonded fluorides in the gamma-phosphate site of T alpha GDP entrap a magnesium counterion and this induces the transconformation to the T alpha GTP form. Fluorides 62-71 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 2384166-5 1990 We propose that at high NaF concentrations, 3 hydrogen-bonded fluorides in the gamma-phosphate site of T alpha GDP entrap a magnesium counterion and this induces the transconformation to the T alpha GTP form. Phosphates 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 2384166-5 1990 We propose that at high NaF concentrations, 3 hydrogen-bonded fluorides in the gamma-phosphate site of T alpha GDP entrap a magnesium counterion and this induces the transconformation to the T alpha GTP form. Guanosine Diphosphate 111-114 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 2384166-5 1990 We propose that at high NaF concentrations, 3 hydrogen-bonded fluorides in the gamma-phosphate site of T alpha GDP entrap a magnesium counterion and this induces the transconformation to the T alpha GTP form. Magnesium 124-133 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 2384166-5 1990 We propose that at high NaF concentrations, 3 hydrogen-bonded fluorides in the gamma-phosphate site of T alpha GDP entrap a magnesium counterion and this induces the transconformation to the T alpha GTP form. Guanosine Triphosphate 199-202 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 2133180-5 1990 Taking a value of 1.00 for F absorption from sodium fluoride (NaF) in water, relative values of 0.58 and 0.32 were obtained for tea ingestion on a fasting stomach, and together with solid food, respectively. Water 70-75 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 2386484-1 1990 In isolated cells from the avian supra-orbital nasal gland, used as a model for exocrine ion secretion, addition of NaF (2-15 mM) produced a slow Al3(+)-enhanced increase in intracellular Ca2+ concn. al3(+) 146-152 C-X-C motif chemokine ligand 8 Homo sapiens 116-119 2163626-1 1990 Potent inhibition of IL-8-induced PBL migration was observed following exposure of PBL to PTX and CTX (1 pM to 0.1 microM), 8-bromo cyclic adenosine monophosphate (cAMP; 1 nM to 1 microM), H7 (1 pM to 0.1 microM), sphingosine (0.1 microM to 100 microM) and the novel pkC inhibitors Ro 31-7549 and Ro 31-8220 (10 pM to 1 microM) for 10 min. 8-Bromo Cyclic Adenosine Monophosphate 124-162 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 2163626-1 1990 Potent inhibition of IL-8-induced PBL migration was observed following exposure of PBL to PTX and CTX (1 pM to 0.1 microM), 8-bromo cyclic adenosine monophosphate (cAMP; 1 nM to 1 microM), H7 (1 pM to 0.1 microM), sphingosine (0.1 microM to 100 microM) and the novel pkC inhibitors Ro 31-7549 and Ro 31-8220 (10 pM to 1 microM) for 10 min. Cyclic AMP 164-168 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 2163626-1 1990 Potent inhibition of IL-8-induced PBL migration was observed following exposure of PBL to PTX and CTX (1 pM to 0.1 microM), 8-bromo cyclic adenosine monophosphate (cAMP; 1 nM to 1 microM), H7 (1 pM to 0.1 microM), sphingosine (0.1 microM to 100 microM) and the novel pkC inhibitors Ro 31-7549 and Ro 31-8220 (10 pM to 1 microM) for 10 min. Sphingosine 214-225 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 2133180-7 1990 Through another bioavailability experiment it was shown that the absorption of F (from MFP) in milk, is as high as that of F (from NaF) in water. Water 139-144 C-X-C motif chemokine ligand 8 Homo sapiens 131-134 1692318-1 1990 Treatment of intact human umbilical vein endothelial cells with NaF results in a dose-dependent biphasic response in both prostacyclin and inositol phosphate production: the stimulation observed with 10-20 mM NaF decreases with higher concentrations. Epoprostenol 122-134 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 2161898-3 1990 Fibrosarcoma-derived MCAF specifically competed with THP-1 (a human monocytic cell line)-derived 125I-labeled MCAF in binding to human PBMC, whereas a similar basic heparin-binding leukocyte chemoattractant, IL-8, did not. Iodine-125 97-101 C-X-C motif chemokine ligand 8 Homo sapiens 208-212 1692318-1 1990 Treatment of intact human umbilical vein endothelial cells with NaF results in a dose-dependent biphasic response in both prostacyclin and inositol phosphate production: the stimulation observed with 10-20 mM NaF decreases with higher concentrations. Epoprostenol 122-134 C-X-C motif chemokine ligand 8 Homo sapiens 209-212 1692318-4 1990 Guanosine 5"-O-(3-thiotriphosphate) (GTP gamma S) also causes a dose-dependent biphasic response in inositol phosphate formation in permeabilized cells and homogenates; a higher inhibitory concentration of GTP gamma S abolishes the stimulation of inositol phosphate production by low NaF concentrations. Guanosine 5'-O-(3-Thiotriphosphate) 0-35 C-X-C motif chemokine ligand 8 Homo sapiens 284-287 1692318-4 1990 Guanosine 5"-O-(3-thiotriphosphate) (GTP gamma S) also causes a dose-dependent biphasic response in inositol phosphate formation in permeabilized cells and homogenates; a higher inhibitory concentration of GTP gamma S abolishes the stimulation of inositol phosphate production by low NaF concentrations. Guanosine 5'-O-(3-Thiotriphosphate) 37-48 C-X-C motif chemokine ligand 8 Homo sapiens 284-287 1692318-1 1990 Treatment of intact human umbilical vein endothelial cells with NaF results in a dose-dependent biphasic response in both prostacyclin and inositol phosphate production: the stimulation observed with 10-20 mM NaF decreases with higher concentrations. Inositol Phosphates 139-157 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 1692318-4 1990 Guanosine 5"-O-(3-thiotriphosphate) (GTP gamma S) also causes a dose-dependent biphasic response in inositol phosphate formation in permeabilized cells and homogenates; a higher inhibitory concentration of GTP gamma S abolishes the stimulation of inositol phosphate production by low NaF concentrations. Inositol Phosphates 100-118 C-X-C motif chemokine ligand 8 Homo sapiens 284-287 1692318-4 1990 Guanosine 5"-O-(3-thiotriphosphate) (GTP gamma S) also causes a dose-dependent biphasic response in inositol phosphate formation in permeabilized cells and homogenates; a higher inhibitory concentration of GTP gamma S abolishes the stimulation of inositol phosphate production by low NaF concentrations. Guanosine Triphosphate 37-40 C-X-C motif chemokine ligand 8 Homo sapiens 284-287 2186041-2 1990 This polypeptide has been iodinated by chloramine-T methodology (350 Ci/mM), and specific receptors for MDNCF/IL-8 have been detected on human neutrophils, U937 cells, THP-1 cells, and dimethyl sulfoxide-differentiated HL-60 cells. Dimethyl Sulfoxide 185-203 C-X-C motif chemokine ligand 8 Homo sapiens 104-109 1692318-1 1990 Treatment of intact human umbilical vein endothelial cells with NaF results in a dose-dependent biphasic response in both prostacyclin and inositol phosphate production: the stimulation observed with 10-20 mM NaF decreases with higher concentrations. Inositol Phosphates 139-157 C-X-C motif chemokine ligand 8 Homo sapiens 209-212 2186041-2 1990 This polypeptide has been iodinated by chloramine-T methodology (350 Ci/mM), and specific receptors for MDNCF/IL-8 have been detected on human neutrophils, U937 cells, THP-1 cells, and dimethyl sulfoxide-differentiated HL-60 cells. Dimethyl Sulfoxide 185-203 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 1692318-4 1990 Guanosine 5"-O-(3-thiotriphosphate) (GTP gamma S) also causes a dose-dependent biphasic response in inositol phosphate formation in permeabilized cells and homogenates; a higher inhibitory concentration of GTP gamma S abolishes the stimulation of inositol phosphate production by low NaF concentrations. Sulfur 47-48 C-X-C motif chemokine ligand 8 Homo sapiens 284-287 1692318-5 1990 A high concentration of NaF furthermore inhibits the non-G-protein-dependent activation of phospholipase C by deoxycholate. Deoxycholic Acid 110-122 C-X-C motif chemokine ligand 8 Homo sapiens 24-27 2186041-5 1990 The receptor for MDNCF/IL-8 is apparently glycosylated since ligand binding is inhibited by the presence of wheat germ agglutinin, a lectin with a binding specificity for N-acetylglucosamine and neuraminic acid. Acetylglucosamine 171-190 C-X-C motif chemokine ligand 8 Homo sapiens 17-22 1692318-2 1990 High concentrations of NaF furthermore reduce thrombin- or A23187-stimulated prostacyclin production. Calcimycin 59-65 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 2186041-5 1990 The receptor for MDNCF/IL-8 is apparently glycosylated since ligand binding is inhibited by the presence of wheat germ agglutinin, a lectin with a binding specificity for N-acetylglucosamine and neuraminic acid. Acetylglucosamine 171-190 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 1692318-6 1990 NaF also induces a dose-dependent biphasic response in cyclic AMP formation in intact cells, indicating that the inhibition of phospholipase C at higher NaF concentrations does not result from a rise in cyclic AMP. Cyclic AMP 55-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 2186041-5 1990 The receptor for MDNCF/IL-8 is apparently glycosylated since ligand binding is inhibited by the presence of wheat germ agglutinin, a lectin with a binding specificity for N-acetylglucosamine and neuraminic acid. Neuraminic Acids 195-210 C-X-C motif chemokine ligand 8 Homo sapiens 17-22 2186041-5 1990 The receptor for MDNCF/IL-8 is apparently glycosylated since ligand binding is inhibited by the presence of wheat germ agglutinin, a lectin with a binding specificity for N-acetylglucosamine and neuraminic acid. Neuraminic Acids 195-210 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 2186041-7 1990 125I-MDNCF/IL-8 bound to human neutrophils is rapidly internalized and subsequently released from cells as trichloroacetic acid-soluble radioactivity. Trichloroacetic Acid 107-127 C-X-C motif chemokine ligand 8 Homo sapiens 5-10 2186041-7 1990 125I-MDNCF/IL-8 bound to human neutrophils is rapidly internalized and subsequently released from cells as trichloroacetic acid-soluble radioactivity. Trichloroacetic Acid 107-127 C-X-C motif chemokine ligand 8 Homo sapiens 11-15 1692318-2 1990 High concentrations of NaF furthermore reduce thrombin- or A23187-stimulated prostacyclin production. Epoprostenol 77-89 C-X-C motif chemokine ligand 8 Homo sapiens 23-26 1692318-3 1990 Direct assay of phospholipase C activity in cell homogenates shows a similar biphasic response to NaF, also after chelation of Ca2+; addition of AlCl3 shifts the inhibition toward lower NaF concentrations. Aluminum Chloride 145-150 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 1692318-3 1990 Direct assay of phospholipase C activity in cell homogenates shows a similar biphasic response to NaF, also after chelation of Ca2+; addition of AlCl3 shifts the inhibition toward lower NaF concentrations. Aluminum Chloride 145-150 C-X-C motif chemokine ligand 8 Homo sapiens 186-189 2096963-1 1990 The formulation for the controlled release of NaF from matrix tablets using Methyl cellulose to prepare chewable NaF tablets for the prevention of dental caries is developed. Methylcellulose 76-92 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 2110856-1 1990 The oral administration of sodium fluoride (NaF) (40 mumol/100 body weight [bw]) to fasting rats produced an immediate fall in insulin levels and the consequent increase in glycemia. Sodium Fluoride 27-42 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 2110856-5 1990 One hour after the intake of 60 mg of NaF, fasting human volunteers showed increased fluoride (5-15 microM) together with a significant fall of plasma insulin levels. Fluorides 85-93 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 2328269-2 1990 Basal and forskolin-stimulated adenylate cyclase activity were significantly lower in the PTSD group whereas aluminum chloride plus sodium fluoride (AlCl3/NaF)- and prostaglandin E1 (PGE1)-stimulated responses were normal. Sodium Fluoride 132-147 C-X-C motif chemokine ligand 8 Homo sapiens 155-158 2096963-1 1990 The formulation for the controlled release of NaF from matrix tablets using Methyl cellulose to prepare chewable NaF tablets for the prevention of dental caries is developed. Methylcellulose 76-92 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 2324203-3 1990 The FRED was shown to act as a signal sequence, targeting NAF to the lumen of the ER, by the fact that NAF acquired N-linked carbohydrate chains. n-linked carbohydrate 116-137 C-X-C motif chemokine ligand 8 Homo sapiens 58-61 2324203-3 1990 The FRED was shown to act as a signal sequence, targeting NAF to the lumen of the ER, by the fact that NAF acquired N-linked carbohydrate chains. n-linked carbohydrate 116-137 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 2324203-6 1990 By using a combination of sedimentation velocity centrifugation and immunoprecipitation assays using polyclonal and conformation-specific monoclonal antibodies it was found that extracellular NAF consisted of a mixture of monomers, disulfide-linked dimers, and tetramers. Disulfides 232-241 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 2329325-4 1990 The decrease in glucose concentration was less with increasing amounts of NaF but could not be totally abolished. Glucose 16-23 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 2182761-4 1990 Tricine-SDS-PAGE analysis gave a single line at Mr 5.3 kD (NAP-1/IL-8 = 5.8 kD). Tricine SDS 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 59-64 2182761-4 1990 Tricine-SDS-PAGE analysis gave a single line at Mr 5.3 kD (NAP-1/IL-8 = 5.8 kD). Tricine SDS 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 2155963-9 1990 Enhancement of PMN anti-Candida activity and release of azurophilic enzymes from PMN by MDNCF/IL-8 were inhibited in the presence of colchicine, which is a known inhibitor of degranulation. Colchicine 133-143 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 2155963-10 1990 These results suggest that MDNCF/IL-8 induced antifungal action of PMN via oxygen-independent pathways. Oxygen 75-81 C-X-C motif chemokine ligand 8 Homo sapiens 27-32 2155963-10 1990 These results suggest that MDNCF/IL-8 induced antifungal action of PMN via oxygen-independent pathways. Oxygen 75-81 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 2155963-11 1990 Furthermore, MDNCF/IL-8 induction of anti-Candida action by PMN was inhibited by pretreatment with Bordetella pertussis toxin, suggesting that enhancement of PMN antifungal activity by MDNCF/IL-8, as well as by FMLP, may be mediated by a GTP-binding protein. Guanosine Triphosphate 238-241 C-X-C motif chemokine ligand 8 Homo sapiens 13-18 2155963-11 1990 Furthermore, MDNCF/IL-8 induction of anti-Candida action by PMN was inhibited by pretreatment with Bordetella pertussis toxin, suggesting that enhancement of PMN antifungal activity by MDNCF/IL-8, as well as by FMLP, may be mediated by a GTP-binding protein. Guanosine Triphosphate 238-241 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 2155963-11 1990 Furthermore, MDNCF/IL-8 induction of anti-Candida action by PMN was inhibited by pretreatment with Bordetella pertussis toxin, suggesting that enhancement of PMN antifungal activity by MDNCF/IL-8, as well as by FMLP, may be mediated by a GTP-binding protein. Guanosine Triphosphate 238-241 C-X-C motif chemokine ligand 8 Homo sapiens 185-190 2155963-11 1990 Furthermore, MDNCF/IL-8 induction of anti-Candida action by PMN was inhibited by pretreatment with Bordetella pertussis toxin, suggesting that enhancement of PMN antifungal activity by MDNCF/IL-8, as well as by FMLP, may be mediated by a GTP-binding protein. Guanosine Triphosphate 238-241 C-X-C motif chemokine ligand 8 Homo sapiens 191-195 2339639-1 1990 To assess whether an interval of a few hours would be advisable between an intake of sodium fluoride (NaF) and that of calcium salts when treating osteoporotic patients with vertebral collapse, we carried out three pharmacokinetic studies in 12 healthy fasting volunteer subjects to compare the fluoride bioavailability provided by NaF alone and NaF combined with two calcium salts. Sodium Fluoride 85-100 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 2339639-1 1990 To assess whether an interval of a few hours would be advisable between an intake of sodium fluoride (NaF) and that of calcium salts when treating osteoporotic patients with vertebral collapse, we carried out three pharmacokinetic studies in 12 healthy fasting volunteer subjects to compare the fluoride bioavailability provided by NaF alone and NaF combined with two calcium salts. Fluorides 92-100 C-X-C motif chemokine ligand 8 Homo sapiens 102-105 2339639-2 1990 The results were as follows: (1) When NaF is accompanied by calcium, the fluoride peak level is lower and delayed. Calcium 60-67 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 2155963-8 1990 However, MDNCF/IL-8 was capable of releasing azurophilic enzymes from cytochalasin B-treated PMN into the extracellular space. Cytochalasin B 70-84 C-X-C motif chemokine ligand 8 Homo sapiens 9-14 2155963-8 1990 However, MDNCF/IL-8 was capable of releasing azurophilic enzymes from cytochalasin B-treated PMN into the extracellular space. Cytochalasin B 70-84 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 2155963-9 1990 Enhancement of PMN anti-Candida activity and release of azurophilic enzymes from PMN by MDNCF/IL-8 were inhibited in the presence of colchicine, which is a known inhibitor of degranulation. Colchicine 133-143 C-X-C motif chemokine ligand 8 Homo sapiens 88-93 2339639-2 1990 The results were as follows: (1) When NaF is accompanied by calcium, the fluoride peak level is lower and delayed. Fluorides 73-81 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 2339624-5 1990 Urinary fluoride levels were higher in the MFP than in the NaF group (9.6 +/- 3.5 vs. 6.8 +/- 3.4 at one year, p = 0.003), suggesting that this difference in efficacy and tolerance is related to a better bioavailability of fluoride provided by MFP than by NaF. Fluorides 8-16 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 2339639-4 1990 (3) The areas under the curves obtained with each of the three preparations were not significantly different, but 24-h urinary fluoride was significantly lower in volunteers receiving simultaneously NaF and calcium salts than in volunteers receiving only NaF. Fluorides 127-135 C-X-C motif chemokine ligand 8 Homo sapiens 199-202 2339640-1 1990 The gastrointestinal absorption of enteric-coated (EC) tablets of sodium fluoride (NaF) with respect to different time schedules of administration of calcium supplements in solution was tested. Sodium Fluoride 66-81 C-X-C motif chemokine ligand 8 Homo sapiens 83-86 2153604-8 1990 The increase of intracellular cAMP levels caused by dibutyryl cAMP (5 x 10(-4) M), Ro-20 1724 (10(-4) M), forskolin (5 x 10(-6) M), NaF (2 x 10(-3) M) reduced, but MIX (5 x 10(-5) M) increased tritium release elicited by ES and K+. Cyclic AMP 30-34 C-X-C motif chemokine ligand 8 Homo sapiens 132-135 2302176-3 1990 With 10 mM-NaF, a concentration unable to induce any measurable Ca2+ mobilization (as measured with Indo 1), addition of AlCl3 potentiated platelet aggregation, thromboxane synthesis, diacylglycerol formation and p43 phosphorylation, without any increase in intracellular Ca2+. Aluminum Chloride 121-126 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 2403554-3 1990 The radiolabeled MDNCF/IL 8 molecules after internalization were proteolytically degraded, and trichloroacetic acid-soluble molecules were released into the culture medium starting at 60 min. Trichloroacetic Acid 95-115 C-X-C motif chemokine ligand 8 Homo sapiens 17-22 2403554-8 1990 Ammonium chloride reduced the MDNCF/IL 8-induced neutrophil chemotactic response in a dose-dependent fashion. Ammonium Chloride 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 30-35 2403554-8 1990 Ammonium chloride reduced the MDNCF/IL 8-induced neutrophil chemotactic response in a dose-dependent fashion. Ammonium Chloride 0-17 C-X-C motif chemokine ligand 8 Homo sapiens 36-40 1966131-0 1990 Production of superoxide anion and hydrogen peroxide by human neutrophilic granulocytes during chemotactic migration towards f-Met-Leu-Phe, C5a, leukotriene B4, monocyte-derived chemotaxin/IL-8 and platelet-activating factor. Superoxides 14-30 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 1966131-0 1990 Production of superoxide anion and hydrogen peroxide by human neutrophilic granulocytes during chemotactic migration towards f-Met-Leu-Phe, C5a, leukotriene B4, monocyte-derived chemotaxin/IL-8 and platelet-activating factor. Hydrogen Peroxide 35-52 C-X-C motif chemokine ligand 8 Homo sapiens 189-193 2161489-2 1990 In the presence of NaF which is a selective inhibitor of 3"----5"-exonuclease center, AMP is an inhibitor of polymerization competitive with respect to dATP. Adenosine Monophosphate 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 2105325-5 1990 Sodium fluoride (NaF), at concentrations known to activate guanine nucleotide regulatory proteins (G proteins), directly stimulated HUVEC PGI2 synthesis in a dose-dependent and time-dependent manner (20 mM NaF, 4.4 +/- 0.5-fold increase at 10 min, 11.9 +/- 1.5-fold increase at 30 min). Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 2105325-5 1990 Sodium fluoride (NaF), at concentrations known to activate guanine nucleotide regulatory proteins (G proteins), directly stimulated HUVEC PGI2 synthesis in a dose-dependent and time-dependent manner (20 mM NaF, 4.4 +/- 0.5-fold increase at 10 min, 11.9 +/- 1.5-fold increase at 30 min). Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 206-209 2105325-5 1990 Sodium fluoride (NaF), at concentrations known to activate guanine nucleotide regulatory proteins (G proteins), directly stimulated HUVEC PGI2 synthesis in a dose-dependent and time-dependent manner (20 mM NaF, 4.4 +/- 0.5-fold increase at 10 min, 11.9 +/- 1.5-fold increase at 30 min). Epoprostenol 138-142 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 2170638-3 1990 Basal, forskolin, A1/NaF- and GppNHp-stimulated cyclic AMP synthesis in membranes from transformed cell lines was identical for schizophrenic and control subjects. Cyclic AMP 48-58 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 2402188-1 1990 In isolated guinea pig gastric chief cells, sodium fluoride (NaF) stimulated a monophasic increase in diacylglycerol accumulation, while cholecystokinin (CCK) strongly stimulated its biphasic accumulation. Sodium Fluoride 44-59 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 2402188-1 1990 In isolated guinea pig gastric chief cells, sodium fluoride (NaF) stimulated a monophasic increase in diacylglycerol accumulation, while cholecystokinin (CCK) strongly stimulated its biphasic accumulation. Diglycerides 102-116 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 2402188-3 1990 Lanthanum chloride (La3+) effectively blocked NaF-stimulated increase in [Ca2+]i, but it blocked only CCK-stimulated late sustained phase of [Ca2+]i increase. lanthanum chloride 0-18 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 2402188-3 1990 Lanthanum chloride (La3+) effectively blocked NaF-stimulated increase in [Ca2+]i, but it blocked only CCK-stimulated late sustained phase of [Ca2+]i increase. lanthanum(3+) 20-24 C-X-C motif chemokine ligand 8 Homo sapiens 46-49 2402188-4 1990 The effect of NaF on pepsinogen secretion was enhanced in the presence of 100 microM AlCl3. Aluminum Chloride 85-90 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 2402188-6 1990 These results suggest that NaF may activate a pertussis-toxin insensitive guanine nucleotide regulatory protein (G protein) coupled to a signal transducing mechanism which seems to be distinct from that activated by CCK, thereby inducing increases in diacylglycerol accumulation, Ca2+ influx and pepsinogen secretion in guinea pig gastric chief cells. Diglycerides 251-265 C-X-C motif chemokine ligand 8 Homo sapiens 27-30 1688564-9 1990 Further, dose-response studies showed that sodium fluoride (NaF), activator of G-binding proteins, and ouabain, inhibitor of Na+/H+ pump, increased levels of IL-6 mRNA. Sodium Fluoride 43-58 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 2161489-2 1990 In the presence of NaF which is a selective inhibitor of 3"----5"-exonuclease center, AMP is an inhibitor of polymerization competitive with respect to dATP. 2'-deoxyadenosine triphosphate 152-156 C-X-C motif chemokine ligand 8 Homo sapiens 19-22 33771440-6 2021 RESULTS: Both conventional hydrogels (etafilcon A, omafilcon A) and two of the four silicone hydrogels tested (balafilcon A, comfilcon A), exhibited some uptake of IL-1beta, IL-8 or TNF-alpha (p < 0.05). Silicones 84-92 C-X-C motif chemokine ligand 8 Homo sapiens 174-178 33814546-8 2021 Aripiprazole was also associated with reduced concentrations of the inflammatory cytokines interleukin-8 and tumor necrosis factor (P < 0.01) during the first 8 weeks of treatment in medication-naive patients with FES. Aripiprazole 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 33807391-0 2021 IL-8 as a Potential Therapeutic Target for Periodontitis and Its Inhibition by Caffeic Acid Phenethyl Ester In Vitro. caffeic acid phenethyl ester 79-107 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 33807391-6 2021 IL-8 mRNA expression was analyzed in saliva-stimulated THP-1 cells treated with CAPE and the heme oxygenase-1 (HO-1) inhibitor tin-protoporphyrin (SnPP). caffeic acid phenethyl ester 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 33807391-6 2021 IL-8 mRNA expression was analyzed in saliva-stimulated THP-1 cells treated with CAPE and the heme oxygenase-1 (HO-1) inhibitor tin-protoporphyrin (SnPP). tin protoporphyrin IX 127-145 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 33807391-6 2021 IL-8 mRNA expression was analyzed in saliva-stimulated THP-1 cells treated with CAPE and the heme oxygenase-1 (HO-1) inhibitor tin-protoporphyrin (SnPP). S-Nitroso-N-propionyl-D,L-penicillamine 147-151 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 33807391-10 2021 However, the IKK inhibitor BMS-345541, NF-kappaB inhibitor BAY 11-7082, and CAPE attenuated saliva-induced IL-8 expression. 3-(4-methylphenylsulfonyl)-2-propenenitrile 59-70 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 33807391-10 2021 However, the IKK inhibitor BMS-345541, NF-kappaB inhibitor BAY 11-7082, and CAPE attenuated saliva-induced IL-8 expression. caffeic acid phenethyl ester 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 33807391-13 2021 The targeted suppression of IL-8 production using CAPE reduces inflammation and periodontitis. caffeic acid phenethyl ester 50-54 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 33779714-8 2021 At the same time, fasudil led to the reduction of IL-1beta, TNF-alpha, IL-6 and IL-8 mRNA levels in insulin-treated cells. fasudil 18-25 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 33777193-7 2021 Furthermore, miR-23 overexpression suppressed inflammation via reducing TNF-alpha, IL-1beta and IL-8 expression levels compared with the NC mimic group. mir-23 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 33589388-1 2021 18F-fluorodeoxyglucose (18F-FDG) and 18F-sodium fluoride (18F-NaF) are front-runners in PET. 18f-sodium fluoride 37-56 C-X-C motif chemokine ligand 8 Homo sapiens 62-65 33589389-1 2021 PET imaging with 18F-sodium fluoride (NaF), combined with computed tomography or magnetic resonance, is a sensitive method of assessing bone turnover. 18f-sodium fluoride 17-36 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 33816157-1 2021 Background: The present study aimed to investigate the clinical implication of F-18 sodium fluoride (NaF) positron emission tomography/computed tomography (PET/CT) for assessing the disease activity of rheumatoid arthritis. f-18 sodium fluoride 79-99 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 33816157-11 2021 Conclusions: Summed joint uptake on F-18 NaF PET/CT had a strong positive correlation with DAS28-ESR and accurately predicted high disease activity. das28-esr 91-100 C-X-C motif chemokine ligand 8 Homo sapiens 41-44 33801712-10 2021 The acrylic resin containing 10 wt% NaF released a high amount of ions over a period of 1 week (1.58 microg/cm2), but the amount of released ions decreased rapidly after 14 days of storage. Acrylic Resins 4-17 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 33815104-4 2021 We showed that METH and HIV-Tat damaged the BBB in vitro, producing abnormal cell morphology, increased apoptosis, reduced protein expression of the tight junctions (TJ) including Junctional adhesion molecule A (JAMA) and Occludin, and a junctional associated protein Zonula occludens 1 (ZO1), and increased the flux of sodium fluorescein (NaF) across the hCMEC/D3 cells monolayer. Methamphetamine 15-19 C-X-C motif chemokine ligand 8 Homo sapiens 340-343 33767939-3 2021 The aim of this study was to investigate the therapeutic effects of the combination of erythropoietin and methylprednisolone in the treatment of ischemia-reperfusion injury to the spinal cord and to analyze its effects on the levels of interleukin-1 beta (IL-1beta), interleukin-1 receptor antagonist (IL-1RA), and interleukin-8 (IL-8). Methylprednisolone 106-124 C-X-C motif chemokine ligand 8 Homo sapiens 315-328 33767939-3 2021 The aim of this study was to investigate the therapeutic effects of the combination of erythropoietin and methylprednisolone in the treatment of ischemia-reperfusion injury to the spinal cord and to analyze its effects on the levels of interleukin-1 beta (IL-1beta), interleukin-1 receptor antagonist (IL-1RA), and interleukin-8 (IL-8). Methylprednisolone 106-124 C-X-C motif chemokine ligand 8 Homo sapiens 330-334 33816541-14 2021 The increase in IL-8 was significantly correlated with decreases in total cholesterol (R 2 = 0.24; P = 0.008), LDL-C (R 2 = 0.17; P = 0.031) and glucose (R 2 = 0.44; P = 0.0001). Cholesterol 74-85 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 33816541-14 2021 The increase in IL-8 was significantly correlated with decreases in total cholesterol (R 2 = 0.24; P = 0.008), LDL-C (R 2 = 0.17; P = 0.031) and glucose (R 2 = 0.44; P = 0.0001). ldl-c 111-116 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 33816541-14 2021 The increase in IL-8 was significantly correlated with decreases in total cholesterol (R 2 = 0.24; P = 0.008), LDL-C (R 2 = 0.17; P = 0.031) and glucose (R 2 = 0.44; P = 0.0001). Glucose 145-152 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 33815104-9 2021 Further, 8-Br-ADPR attenuated the effects of METH and HIV-Tat on the BBB in tree shrews-namely, down-regulated TJ protein expression and increased BBB permeability to Evans blue (EB) and NaF. 8-br-adpr 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 187-190 33815104-6 2021 Pretreatment with n-acetylcysteine amide (NACA) alleviated the oxidative stress response and BBB damage characterized by improving cell morphology, viability, apoptosis levels, TJ protein expression levels, and NaF flux. N-Acetylcysteinamide 18-40 C-X-C motif chemokine ligand 8 Homo sapiens 211-214 33815104-6 2021 Pretreatment with n-acetylcysteine amide (NACA) alleviated the oxidative stress response and BBB damage characterized by improving cell morphology, viability, apoptosis levels, TJ protein expression levels, and NaF flux. N-Acetylcysteinamide 42-46 C-X-C motif chemokine ligand 8 Homo sapiens 211-214 33798967-9 2021 The results of the autopsy and laboratory tests in the present cases and those of cultured cell experiments indicated that CNS disorders caused by CNS stimulants such as amphetamines led to changes in IL-6 as an immune response, which suggests that IL-8 may help protect nerve cells in cases involving heat stroke and stimulants. Amphetamines 170-182 C-X-C motif chemokine ligand 8 Homo sapiens 249-253 33767707-7 2021 Compared to that in control patients, the expression of interleukin (IL)-8 and TLR7 pathway molecules in B-cells was higher in patients with pSS-associated thrombocytopenia. pss 141-144 C-X-C motif chemokine ligand 8 Homo sapiens 56-74 33778274-8 2021 Results: First, the reduced mitochondrial membrane potential (DeltaPsim) and secretion of proinflammatory factors (IL-1beta, IL-8, and MCP-1) induced by TNF-alpha were significantly reversed by treatment with Feprazone. Feprazone 209-218 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 32796483-1 2020 OBJECTIVES: To evaluate the interobserver agreement and the diagnostic performance in F-sodium fluoride (F-NaF) PET/computed tomography (CT) for the detection of skull-base bone invasion (SBBI) and osseous metastases in patients with newly diagnosed nasopharyngeal carcinoma (NPC). f-sodium fluoride 86-103 C-X-C motif chemokine ligand 8 Homo sapiens 107-110 33778827-10 2020 The results of ELLISA and Western blot showed that compared with the untreated group, the treatment groups inhibited the expression of inflammatory factors IL-6, IL-1beta and TNF-alpha, and promoted the expression of IL-8, and the effect of EDTA+HA group was much more significant(P<0.05). Edetic Acid 241-245 C-X-C motif chemokine ligand 8 Homo sapiens 217-221 33807929-5 2021 Losartan attenuated the AT-II-stimulated production of vascular endothelial growth factor-A (VEGF-A) and interleukin-8 and suppressed lenvatinib-mediated autocrine VEGF-A production in HCC cells. Losartan 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 105-118 33379200-7 2020 Iron oxide increased IL-8 production while silica also induced significant production of IL-1beta. ferric oxide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 33379200-8 2020 Both iron oxide and silica enhanced LPS-induced production of TNF-alpha, IL-1beta, IL-6 and IL-8 in THP-1 cells with most of these responses replicated in PBMCs. ferric oxide 5-15 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 33379200-8 2020 Both iron oxide and silica enhanced LPS-induced production of TNF-alpha, IL-1beta, IL-6 and IL-8 in THP-1 cells with most of these responses replicated in PBMCs. Silicon Dioxide 20-26 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 33237239-12 2020 An application of topical NaF varnishes was effective in reducing TSL and enamel roughness after erosion challenges, being the CCP-ACP/NaF varnish more effective than NaF varnish and water after 3 days of erosion. ccp 127-130 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 33237239-12 2020 An application of topical NaF varnishes was effective in reducing TSL and enamel roughness after erosion challenges, being the CCP-ACP/NaF varnish more effective than NaF varnish and water after 3 days of erosion. acp 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 33237239-12 2020 An application of topical NaF varnishes was effective in reducing TSL and enamel roughness after erosion challenges, being the CCP-ACP/NaF varnish more effective than NaF varnish and water after 3 days of erosion. Water 183-188 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 33033709-7 2020 Notably, the mRNA level of interleukin-8 (IL-8)/CXCL8 was highly elevated in 15d-PGJ2-stimulated MCF-7 cells. 9-deoxy-delta-9-prostaglandin D2 81-85 C-X-C motif chemokine ligand 8 Homo sapiens 27-40 33033709-7 2020 Notably, the mRNA level of interleukin-8 (IL-8)/CXCL8 was highly elevated in 15d-PGJ2-stimulated MCF-7 cells. 9-deoxy-delta-9-prostaglandin D2 81-85 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 33033709-7 2020 Notably, the mRNA level of interleukin-8 (IL-8)/CXCL8 was highly elevated in 15d-PGJ2-stimulated MCF-7 cells. 9-deoxy-delta-9-prostaglandin D2 81-85 C-X-C motif chemokine ligand 8 Homo sapiens 48-53 33033709-8 2020 15d-PGJ2-induced up-regulation of IL-8/CXCL8 expression was abrogated by silencing of Snail short interfering RNA. 15-deoxy-delta(12,14)-prostaglandin J2 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 33033709-8 2020 15d-PGJ2-induced up-regulation of IL-8/CXCL8 expression was abrogated by silencing of Snail short interfering RNA. 15-deoxy-delta(12,14)-prostaglandin J2 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 39-44 33033709-11 2020 Taken together, above findings suggest that 15d-PGJ2 induces EMT through up-regulation of Snail expression and subsequent production of CXCL8 as a putative activator of fibroblasts, which may contribute to tumor-stroma interaction in inflammatory breast cancer microenvironment. 9-deoxy-delta-9-prostaglandin D2 48-52 C-X-C motif chemokine ligand 8 Homo sapiens 136-141 33824247-3 2020 TCS markedly downregulated IL-6, IL-8, and IL-15 in human periodontal ligament fibroblasts (HPDLFs) treated with LPS-PG. Triclosan 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 29261619-2 2018 Bone scintigraphy with [Tc]hydroxymethylene diphosphonate (Tc-HDP) and [F]sodium fluoride (F-NaF) have been investigated in the noninvasive diagnosis of transthyretin (ATTR)-related cardiac amyloidosis. [f]sodium fluoride 71-89 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 32244040-7 2020 THC and CBD (both at 10 muM) attenuated TLR3/4-induced IRF3 activation and induction of CXCL10/IFN-beta, while both phytocannabinoids failed to impact TLR4-induced IkappaB-alpha degradation and TNF-alpha/CXCL8 expression. Dronabinol 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 204-209 32244040-7 2020 THC and CBD (both at 10 muM) attenuated TLR3/4-induced IRF3 activation and induction of CXCL10/IFN-beta, while both phytocannabinoids failed to impact TLR4-induced IkappaB-alpha degradation and TNF-alpha/CXCL8 expression. Cannabidiol 8-11 C-X-C motif chemokine ligand 8 Homo sapiens 204-209 29743070-3 2018 We have previously demonstrated that hydrogen sulfide (H2S) can inhibit ASM cell proliferation and CXCL8 release, from cells isolated from non-smokers. Hydrogen Sulfide 37-53 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 29743070-3 2018 We have previously demonstrated that hydrogen sulfide (H2S) can inhibit ASM cell proliferation and CXCL8 release, from cells isolated from non-smokers. Hydrogen Sulfide 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 99-104 29743070-6 2018 Proliferation and cytokine release (IL-6 and CXCL8) of ASM was induced by FCS, and measured by bromodeoxyuridine incorporation and ELISA, respectively. Bromodeoxyuridine 95-112 C-X-C motif chemokine ligand 8 Homo sapiens 45-50 26820827-6 2016 5-HT-induced elevation of IL-8 at both mRNA and protein levels was observed, which was inhibited by TEMPOL (a free radical scavenger), and inhibitors for p38 MAPK (SB203580) and ERK (U0126), in line with the time-dependent phosphorylation of p38 MAPK and ERK. tempol 100-106 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 26246181-0 2016 Poly-L-Arginine Acts Synergistically with LPS to Promote the Release of IL-6 and IL-8 via p38/ERK Signaling Pathways in NCI-H292 Cells. polyarginine 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 81-85 26246181-2 2016 The pharmacological function of MBP can be mimicked by poly-L-arginine (PLA), however, the potential signaling mechanisms of LPS-PLA-induced release of the inflammatory cytokines interleukin (IL)-6 and IL-8 remain unclear. polyarginine 55-70 C-X-C motif chemokine ligand 8 Homo sapiens 202-206 26295910-8 2015 Finally, the analysis of blood specimens stored with and without preservatives in both groups suggests that specimens stored with NaF/KOx maintain mephedrone stability better than those stored with EDTA (p<0.001) and those stored without preservatives (p<0.0001), therefore, we strongly recommend in order to maintain the highest mephedrone stability in blood, to store specimens at -20 C adding NaF/KOx as preservative. mephedrone 147-157 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 25589619-6 2015 Dabrafenib and trametinib in BRAF V600E/K, and trametinib in BRAF wild-type tumor cells induced apoptosis markers, upregulated HLA molecule expression, and downregulated certain immunosuppressive factors such as PD-L1, IL1, IL8, NT5E, and VEGFA. trametinib 47-57 C-X-C motif chemokine ligand 8 Homo sapiens 224-227 24099766-0 2013 NOD2 triggers PGE2 synthesis leading to IL-8 activation in Staphylococcus aureus-infected human conjunctival epithelial cells. Dinoprostone 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 24099766-2 2013 As in some cell types both the bacteria may induce the release of prostaglandin E2 (PGE2) and PGE2 may affect the expression of IL-8, we aimed at investigating whether in human conjunctival cells infected with S. aureus or P. aeruginosa the activation of IL-8 transcription was mediated by PGE2 and which were the underlying molecular mechanisms. Dinoprostone 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 24099766-2 2013 As in some cell types both the bacteria may induce the release of prostaglandin E2 (PGE2) and PGE2 may affect the expression of IL-8, we aimed at investigating whether in human conjunctival cells infected with S. aureus or P. aeruginosa the activation of IL-8 transcription was mediated by PGE2 and which were the underlying molecular mechanisms. Dinoprostone 94-98 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 24099766-3 2013 We found that S. aureus, but not P. aeruginosa, triggered IL-8 activation by increasing COX-2 expression and PGE2 levels in a time-dependent manner. Dinoprostone 109-113 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 23861935-7 2013 Stimulation with the corresponding agonists Pam3CSK4, poly(I:C), LPS, R-837 and iE-DAP, respectively, induced IL-6, IL-8 and GM-CSF release and up-regulation of ICAM-1 and HLA-DR, while poly(I:C) also affected the release of eotaxin and RANTES. alpha,beta-diacryloxypropionic acid 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 27667548-5 2016 Furthermore, baicalein blocked the TNF-alpha-induced expression of NF-kappaB target genes involved in anti-apoptosis (cIAP-1, cIAP-2, FLIP and BCL-2), proliferation (COX-2, cyclin D1 and c-Myc), invasion (MMP-9), angiogenesis (VEGF) and major inflammatory cytokines (IL-8 and MCP1). baicalein 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 267-271 25589619-6 2015 Dabrafenib and trametinib in BRAF V600E/K, and trametinib in BRAF wild-type tumor cells induced apoptosis markers, upregulated HLA molecule expression, and downregulated certain immunosuppressive factors such as PD-L1, IL1, IL8, NT5E, and VEGFA. dabrafenib 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 224-227 26820827-6 2016 5-HT-induced elevation of IL-8 at both mRNA and protein levels was observed, which was inhibited by TEMPOL (a free radical scavenger), and inhibitors for p38 MAPK (SB203580) and ERK (U0126), in line with the time-dependent phosphorylation of p38 MAPK and ERK. SB 203580 164-172 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 20218345-8 2010 CONCLUSION: LX inhibits TLR-mediated production of both proinflammatory (IL-1, IL-6, IL-8, IL-12, TNFalpha) and anti-inflammatory (IL-10) cytokinesby PBMC of healthy subjects in vitro. lx 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 26820827-6 2016 5-HT-induced elevation of IL-8 at both mRNA and protein levels was observed, which was inhibited by TEMPOL (a free radical scavenger), and inhibitors for p38 MAPK (SB203580) and ERK (U0126), in line with the time-dependent phosphorylation of p38 MAPK and ERK. U 0126 183-188 C-X-C motif chemokine ligand 8 Homo sapiens 26-30 9860036-8 1998 Within-treatment comparisons suggested that mometasone furoate reduced the antigen-induced late-phase response for IL-6, IL-8, and eosinophils compared with pretreatment. Mometasone Furoate 44-62 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 19180502-10 2009 After up-regulation of NOD-2 by TLR ligands, its ligand muramyl dipeptide (MDP) increased the expression of IL-6 and IL-8 via p38 and NF-kappaB. Acetylmuramyl-Alanyl-Isoglutamine 56-73 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 19180502-10 2009 After up-regulation of NOD-2 by TLR ligands, its ligand muramyl dipeptide (MDP) increased the expression of IL-6 and IL-8 via p38 and NF-kappaB. Acetylmuramyl-Alanyl-Isoglutamine 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 9269788-7 1997 Compared with vehicle control, pretreatment with SDZ MRL 953 markedly reduced the release of TNF-alpha, IL-1beta, IL-8, IL-6, and G-CSF, but augmented the increase in granulocyte counts to endotoxin. Sulfadiazine 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 16946614-0 2006 The protective effect of TiF4, SnF2 and NaF on erosion of enamel by hydrochloric acid in vitro measured by white light interferometry. Hydrochloric Acid 68-85 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 14561211-13 2002 It has been shown that macrolides inhibit the production of IL-8 and IL-1beta and the expression of ICAM-1, suggesting that macrolides block the aforementioned dual positive feedback system of neutrophil recruitment and thereby exert their clinical efficacy in the treatment of chronic sinusitis. Macrolides 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 14561211-13 2002 It has been shown that macrolides inhibit the production of IL-8 and IL-1beta and the expression of ICAM-1, suggesting that macrolides block the aforementioned dual positive feedback system of neutrophil recruitment and thereby exert their clinical efficacy in the treatment of chronic sinusitis. Macrolides 124-134 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 8584542-5 1995 When compared to air-exposed cells, NO2 induced increases in IL-6 (23.4-fold) and IL-8 (30.9-fold) mRNA abundance. Nitrogen Dioxide 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 9860036-11 1998 CONCLUSION: These results suggest that the clinical activity of mometasone furoate nasal spray in seasonal allergic rhinitis is likely due, in part, to a reduction in the levels of histamine in nasal secretions related to the early phase response, and reductions in IL-6, IL-8, and eosinophils during the late phase response. Mometasone Furoate 64-82 C-X-C motif chemokine ligand 8 Homo sapiens 272-276 8584542-6 1995 The NO2-dependent increases in mRNA expression reached a maximum between 0 and 1 h post exposure and returned to baseline levels within 24 h. IL-6 and IL-8 proteins as measured by enzyme-linked immunosorbent assays (ELISA) were also elevated in supernatants recovered from NO2-exposed BEAS-2B cells. Nitrogen Dioxide 4-7 C-X-C motif chemokine ligand 8 Homo sapiens 151-155 9860036-11 1998 CONCLUSION: These results suggest that the clinical activity of mometasone furoate nasal spray in seasonal allergic rhinitis is likely due, in part, to a reduction in the levels of histamine in nasal secretions related to the early phase response, and reductions in IL-6, IL-8, and eosinophils during the late phase response. Histamine 181-190 C-X-C motif chemokine ligand 8 Homo sapiens 272-276 34289309-11 2022 Furthermore, CD142 silencing-induced IL-8 degradation was recovered by treatment of autophagy inhibitor 3-MA. 3-methyladenine 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 34609586-10 2022 In the exposed group a positive correlation between serum copper, arsenic and serum ICAM and IL8 was found. Copper 58-64 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 34609586-10 2022 In the exposed group a positive correlation between serum copper, arsenic and serum ICAM and IL8 was found. Arsenic 66-73 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 34609586-13 2022 CONCLUSION: Occupational exposure to copper and arsenic was associated with ventilatory and radiological impairment, with a corresponding increase in the serum level of ICAM-1 and IL8, which can be used as biomarkers for pulmonary impairment among copper smelter workers. Copper 37-43 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 34609586-13 2022 CONCLUSION: Occupational exposure to copper and arsenic was associated with ventilatory and radiological impairment, with a corresponding increase in the serum level of ICAM-1 and IL8, which can be used as biomarkers for pulmonary impairment among copper smelter workers. Arsenic 48-55 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 34609586-13 2022 CONCLUSION: Occupational exposure to copper and arsenic was associated with ventilatory and radiological impairment, with a corresponding increase in the serum level of ICAM-1 and IL8, which can be used as biomarkers for pulmonary impairment among copper smelter workers. Copper 248-254 C-X-C motif chemokine ligand 8 Homo sapiens 180-183 34844316-7 2022 Inflammatory response analysis revealed BCB combustion aerosols to cause a mild increase in CXCL1 and CXCL8 levels, but in the case of SPR combustion aerosol, a decrease compared to control was observed. Bromocholine bromide 40-43 C-X-C motif chemokine ligand 8 Homo sapiens 102-107 34890707-0 2022 Nicotine stimulates IL-8 expression via ROS/NF-kappaB and ROS/MAPK/AP-1 axis in human gastric cancer cells. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 34890707-3 2022 The role of nicotine in IL-8 expression and the underlying mechanism is currently unknown. Nicotine 12-20 C-X-C motif chemokine ligand 8 Homo sapiens 24-28 34890707-4 2022 Here, we examined the effects of nicotine on IL-8 expression and explored the potential mechanisms in gastric cancer cells. Nicotine 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 34890707-5 2022 We found that nicotine increases IL-8 expression. Nicotine 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 33-37 34890707-9 2022 AGS gastric cancer cells pretreated with nicotine stimulate angiogenesis in the tumor microenvironment, partially abrogated by silencing IL-8 in AGS cells. Nicotine 41-49 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 34890707-10 2022 In this study, we found that nicotine induces IL-8 expression via ROS/NF-kappaB and ROS/MAPK (Erk1/2, p38)/AP-1 axis in gastric cancer cells, thus stimulating endothelial cell proliferation and angiogenesis in the tumor microenvironment. Nicotine 29-37 C-X-C motif chemokine ligand 8 Homo sapiens 46-50 34800781-0 2022 The modulating effect of methoxy-derivatives of 2"-hydroxychalcones on the release of IL-8, MIF, VCAM-1 and ICAM-1 by colon cancer cells. 2'-hydroxychalcone 48-67 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 34971958-10 2022 The p38 inhibitor SB203580 inhibited the secretion of IL-8, slightly inhibited the secretion of IL-6, and did not affect NF-kappaB activity. SB 203580 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 34781073-2 2022 DESIGN: Ameloblast-like cells (LS8 cells) were exposed to various concentrations of sodium fluoride (NaF) for up to 48 h. Runx2 expression was downregulated by gene silencing, and Foxo1 expression was up- and downregulated by gene overexpression and silencing, respectively. Sodium Fluoride 84-99 C-X-C motif chemokine ligand 8 Homo sapiens 101-104 34781073-10 2022 CONCLUSION: The results indicated that NaF reduces Runx2 expression in LS8 cells and that decreased Foxo1/Runx2 expression induced by high fluoride is a cause of low KLK4 expression. Fluorides 139-147 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 34236247-9 2022 17,18-EpETE significantly inhibited tumor necrosis factor (TNF)-alpha-induced production of interleukin (IL)-6 , IL-8, and mucin from cultured human airway epithelial cells dose dependently, and these antiinflammatory effects on cytokine production were abolished by GW1100, a selective GPR40 antagonist. 17,18-epoxy-5,8,11,14-eicosatetraenoic acid 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 34236247-9 2022 17,18-EpETE significantly inhibited tumor necrosis factor (TNF)-alpha-induced production of interleukin (IL)-6 , IL-8, and mucin from cultured human airway epithelial cells dose dependently, and these antiinflammatory effects on cytokine production were abolished by GW1100, a selective GPR40 antagonist. GW1100 267-273 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 34593533-2 2022 METHODS: We performed 18F-sodium fluoride (18F-NaF) positron emission tomography/CT in patients with mild to moderate AS (peak aortic jet velocity between 2 and 4 m/s) and high versus low Lp(a) (>50 mg/dL vs <50 mg/dL, respectively). 18f-sodium fluoride 22-41 C-X-C motif chemokine ligand 8 Homo sapiens 47-50 34593533-10 2022 Linear regression analysis showed valvular calcium score to be the only significant determinant of valvular 18F-NaF uptake (beta=0.63; 95% CI 0.38 to 0.88 per 1000 Agatston unit increase, p<0.001). Calcium 43-50 C-X-C motif chemokine ligand 8 Homo sapiens 112-115 34763226-3 2022 At present, the objective of this study was to investigate the relationship between down-regulation of IKBKG gene expression and hepatocyte senescence induced by sodium fluoride (NaF). Sodium Fluoride 162-177 C-X-C motif chemokine ligand 8 Homo sapiens 179-182 34614305-11 2022 RESULTS: Imiquimod significantly inhibited the activity of tyrosinase activity and decreased melanin content in melanocytes and significantly increased apoptosis and IL-6, IL-8, and sICAM-1 production in melanocytes. Imiquimod 9-18 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 34170488-4 2022 We aimed to study the effect of RGZ onto inflammation-induced secretion of CXCL10, IFNgamma, TNFalpha, interleukin (IL)-6 and IL-8 by human CD4 + T and DCs, and onto IFNgamma/TNFalpha-dependent signaling in human cardiomyocytes associated with chemokine release. Rosiglitazone 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 34170488-8 2022 In human cardiomyocytes, RGZ impaired IFNgamma/TNFalpha signal transduction, blocking the phosphorylation/nuclear translocation of signal transducer and activator of transcription 1 (Stat1) and nuclear factor-kB (NF-kB), in association with a significant decrease in CXCL10 expression, IL-6 and IL-8 release. Rosiglitazone 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 295-299 34755269-11 2022 After colchicine treatment, patients had higher BUN and lower serum levels of IL-8, IL-12p70, and IL-17A. Colchicine 6-16 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 34651203-15 2022 HIF-1 activation increased IL-1beta and IL-8 in human uroepithelial cells treated with high glucose concentration. Glucose 92-99 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 34763226-7 2022 RESULTS: The number of senescence-positive cells in rat liver tissues was increased as well as the level of IL-8 and the expression levels of p16, p21 and IKBKG in fluoride exposure to rat depending on the fluoride concentration. Fluorides 164-172 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 34763226-7 2022 RESULTS: The number of senescence-positive cells in rat liver tissues was increased as well as the level of IL-8 and the expression levels of p16, p21 and IKBKG in fluoride exposure to rat depending on the fluoride concentration. Fluorides 206-214 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 34838662-8 2022 Long time to return of spontaneous circulation and high lactate level at admission were associated with increased complement activation (TCC and C3bc), pro-inflammatory cytokines (IL-6, IL-8) and endothelial injury (syndecan-1) at admission. Lactic Acid 56-63 C-X-C motif chemokine ligand 8 Homo sapiens 186-190 34883095-6 2022 Moreover, exposure to DPAA at 50 microM for 96 h or 10 microM for 288 h in NHA induced hypersecretion of cytokines induced in DPAA-exposed NRA (MCP-1, adrenomedullin, FGF-2, CXCL1, and IL-6), and IL-8 besides into culture medium. diphenylarsinic acid 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 34883095-6 2022 Moreover, exposure to DPAA at 50 microM for 96 h or 10 microM for 288 h in NHA induced hypersecretion of cytokines induced in DPAA-exposed NRA (MCP-1, adrenomedullin, FGF-2, CXCL1, and IL-6), and IL-8 besides into culture medium. nha 75-78 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 34930349-1 2021 BACKGROUND: To investigate the role of adenosine monophosphate (AMP)-activated protein kinase (AMPK) on the production of interleukin (IL)-8, monocyte chemoattractant protein (MCP)-1, prostaglandin E2 and F2alpha induced by IL-1beta in endometrial stromal cells (ESCs) following treatment with 5-aminoimidazole-4- carboxamide ribonucleoside (AICAR). 5-aminoimidazole-4- carboxamide ribonucleoside 294-340 C-X-C motif chemokine ligand 8 Homo sapiens 122-140 34936813-8 2022 mTOR inhibitor rapamycin significantly suppressed the elevation of IL-6, IL-8, and VEGF stimulated by 7-KC. Sirolimus 15-24 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 34936813-10 2022 Conclusions: Inhibition of mTOR signaling pathway suppressed the elevation of inflammatory cytokines IL-6, IL-8, and the angiogenic agent VEGF induced by 7-KC. 7-ketocholesterol 154-158 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 34930349-1 2021 BACKGROUND: To investigate the role of adenosine monophosphate (AMP)-activated protein kinase (AMPK) on the production of interleukin (IL)-8, monocyte chemoattractant protein (MCP)-1, prostaglandin E2 and F2alpha induced by IL-1beta in endometrial stromal cells (ESCs) following treatment with 5-aminoimidazole-4- carboxamide ribonucleoside (AICAR). Adenosine 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 122-140 34930349-1 2021 BACKGROUND: To investigate the role of adenosine monophosphate (AMP)-activated protein kinase (AMPK) on the production of interleukin (IL)-8, monocyte chemoattractant protein (MCP)-1, prostaglandin E2 and F2alpha induced by IL-1beta in endometrial stromal cells (ESCs) following treatment with 5-aminoimidazole-4- carboxamide ribonucleoside (AICAR). Adenosine Monophosphate 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 122-140 34941893-5 2021 Additionally, high concentrations of capsaicin (0.02-2 mM) damage enterocytes (Caco-2 and HT-29) as indicated by cell viability test, supernatant cytokine (IL-8), transepithelial electrical resistance (TEER) and transepithelial FITC-dextran (4.4 kDa) but were attenuated by Lactobacillus condition media (LCM) from both probiotic-strains. Capsaicin 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 34930349-1 2021 BACKGROUND: To investigate the role of adenosine monophosphate (AMP)-activated protein kinase (AMPK) on the production of interleukin (IL)-8, monocyte chemoattractant protein (MCP)-1, prostaglandin E2 and F2alpha induced by IL-1beta in endometrial stromal cells (ESCs) following treatment with 5-aminoimidazole-4- carboxamide ribonucleoside (AICAR). acadesine 342-347 C-X-C motif chemokine ligand 8 Homo sapiens 122-140 34930349-3 2021 We examined the effects of IL-1beta, IL-1 ra and AICAR on the production of IL-8, MCP-1, PGE2 and PGF2alpha in human ESCs. Radium 42-44 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 34930349-3 2021 We examined the effects of IL-1beta, IL-1 ra and AICAR on the production of IL-8, MCP-1, PGE2 and PGF2alpha in human ESCs. acadesine 49-54 C-X-C motif chemokine ligand 8 Homo sapiens 76-80 34977169-8 2021 Results: AEDPPE significantly promoted the migration and invasion of HTR-8/SVneo cells, and it decreased the expression of interleukins 1 beta (IL-1beta), interleukin 6 (IL-6), and interleukin 8 (IL-8). aedppe 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 181-194 34977169-8 2021 Results: AEDPPE significantly promoted the migration and invasion of HTR-8/SVneo cells, and it decreased the expression of interleukins 1 beta (IL-1beta), interleukin 6 (IL-6), and interleukin 8 (IL-8). aedppe 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 196-200 34975472-0 2021 UDCA Inhibits Hypoxic Hepatocellular Carcinoma Cell-Induced Angiogenesis Through Suppressing HIF-1alpha/VEGF/IL-8 Intercellular Signaling. Ursodeoxycholic Acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 34918964-8 2021 Results: Our findings showed that inhalation of CBD was able to not only limit the tumor growth but also to alter the dynamics of TME by repressing P-selectin, apelin, and interleukin (IL)-8, as well as blocking a key immune checkpoint-indoleamine 2,3-dioxygenase (IDO). Cannabidiol 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 172-190 34943253-8 2021 Exposure to low doses of CAP enhanced the proliferation rate of cells and stimulated the expression of key genes (KGF, MMP2, GMCSF, IL-6, and IL-8) in fibroblasts, indicating the activation and initiation of the skin repair process. cap 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 34975472-7 2021 In HCC cells, UDCA inhibited hypoxia-induced upregulation of VEGF and IL-8 both in mRNA and protein levels. Ursodeoxycholic Acid 14-18 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 34975889-0 2021 Antcin K Inhibits TNF-alpha, IL-1beta and IL-8 Expression in Synovial Fibroblasts and Ameliorates Cartilage Degradation: Implications for the Treatment of Rheumatoid Arthritis. antcin K 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 34975472-8 2021 UDCA also inhibited IL-8-induced angiogenesis in vitro and in vivo through suppressing IL-8-induced phosphorylation of ERK. Ursodeoxycholic Acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 20-24 34975889-3 2021 In our analysis of the mechanism of action, Antcin K inhibited the expression of three cytokines (tumor necrosis factor alpha (TNF-alpha), interleukin 1 beta (IL-1beta) and IL-8) in human RASFs; cytokines that are crucial to RA synovial inflammation. antcin K 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 34975472-8 2021 UDCA also inhibited IL-8-induced angiogenesis in vitro and in vivo through suppressing IL-8-induced phosphorylation of ERK. Ursodeoxycholic Acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 87-91 34975889-6 2021 The inhibitory effects of Antcin K upon TNF-alpha, IL-1beta and IL-8 expression in human RASFs was achieved through the downregulation of the FAK, PI3K, AKT and NF-kappaB signaling cascades. antcin K 26-34 C-X-C motif chemokine ligand 8 Homo sapiens 64-68 34975472-12 2021 Transfection of the HIF-1alpha overexpression plasmid reversed the effects of UDCA on hypoxic HCC cell-induced angiogenesis, HRE activity, and expressions of IL-8 and VEGF. Ursodeoxycholic Acid 78-82 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 34975472-13 2021 Conclusions: Our results demonstrated that UDCA could inhibit hypoxic HCC cell-induced angiogenesis through suppressing HIF-1alpha/VEGF/IL-8-mediated intercellular signaling between HCC cells and endothelial cells. Ursodeoxycholic Acid 43-47 C-X-C motif chemokine ligand 8 Homo sapiens 136-140 34915624-14 2021 In addition, MSC may improve the steroid resistance by reducing the expression of IL-8. Steroids 33-40 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 34944509-11 2021 High doses of vitamin D supplementation led to a significant decrease in pro-inflammatory cytokines (IFN- , TNF-alpha, IL-1beta, IL-6, IL-8, and IL-17) and high-sensitivity C-reactive protein (hsCRP), whereas the production of anti-inflammatory cytokines (IL-10, IL-5) was up-regulated. Vitamin D 14-23 C-X-C motif chemokine ligand 8 Homo sapiens 135-139 34886812-12 2021 Simultaneously, acacetin reduced mesothelial cell-induced transcripts and production of pro-inflammatory cytokine IL-6 and IL-8 in ovarian cancer cells. acacetin 16-24 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 34943075-12 2021 Our results revealed that administration of Rg3 diminished the production of interleukin 8 (IL-8) and matrix metallopeptidase 9 (MMP-9) in chondrocytes via SIRT1/PGC-1alpha/SIRT3/p38 MAPK/NF-kappaB signaling in response to TNF-alpha stimulation. ginsenoside Rg3 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 77-90 34943075-12 2021 Our results revealed that administration of Rg3 diminished the production of interleukin 8 (IL-8) and matrix metallopeptidase 9 (MMP-9) in chondrocytes via SIRT1/PGC-1alpha/SIRT3/p38 MAPK/NF-kappaB signaling in response to TNF-alpha stimulation. ginsenoside Rg3 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 34888674-9 2022 Also, NAA/Cr ratio was positively correlated with circulating IL-8 levels (rho = 0.26, P = 0.04). N-acetylaspartate 6-9 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 34888674-9 2022 Also, NAA/Cr ratio was positively correlated with circulating IL-8 levels (rho = 0.26, P = 0.04). Chromium 10-12 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 34959964-6 2021 RESULTS: Vivomixx supplementation induced a better response to PCV13 immunization, as shown by greater change in anti-Pn CPS13 IgG and increase in salivary IgA, IL-10 and IL-8. vivomixx 9-17 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 34957146-8 2021 The levels of IL-8 and TNF-alpha were positively correlated with OSDI scores (p = 0.046, p = 0.043, respectively) and negatively correlated with f-NIKBUT and FBUT (p = 0.026, p = 0.006, respectively). fbut 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 14-18 34950134-8 2021 Imiquimod also reduced poly(I:C)-induced pro-inflammatory cytokines including IL-1beta, IL-6, IL-8, and IL-33. Imiquimod 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 34956864-6 2021 Results: In pre-treatment biopsies, TREM1 and known TREM-1 inducible cytokines (IL1B, IL8) were discovered by a statistical ranking procedure as top genes for which high expression was associated with reduced response to NAC, but only in the context of immunologically "hot" tumors otherwise associated with a high NAC response rate. nac 221-224 C-X-C motif chemokine ligand 8 Homo sapiens 86-89 34943719-6 2021 Herein, we demonstrated that dexamethasone binds with high affinity to interlukin-1 (IL-1), IL-6, IL-8, IL-12, IL-21, INF2, TGFbeta-1, INF-gamma, CXCL8, some of the receptors, IL-1R, IL-21R, IFNGR, INFAR, IL-6alphaR-gp130, ST2 and the SARS-CoV-2 protein NSP macro X, and 3CLpro, forming stable drug-protein complexes. Dexamethasone 29-42 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 34943719-6 2021 Herein, we demonstrated that dexamethasone binds with high affinity to interlukin-1 (IL-1), IL-6, IL-8, IL-12, IL-21, INF2, TGFbeta-1, INF-gamma, CXCL8, some of the receptors, IL-1R, IL-21R, IFNGR, INFAR, IL-6alphaR-gp130, ST2 and the SARS-CoV-2 protein NSP macro X, and 3CLpro, forming stable drug-protein complexes. Dexamethasone 29-42 C-X-C motif chemokine ligand 8 Homo sapiens 146-151 34950134-8 2021 Imiquimod also reduced poly(I:C)-induced pro-inflammatory cytokines including IL-1beta, IL-6, IL-8, and IL-33. Poly I-C 23-32 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 34878076-1 2021 This randomized three-armed controlled clinical trial compared the effect of titanium tetrafluoride (TiF4) and sodium fluoride (NaF) varnishes on caries control in smooth surfaces of permanent dentition and children"s acceptability. Sodium Fluoride 111-126 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 34941711-0 2021 Indoxyl Sulfate Elevated Lnc-SLC15A1-1 Upregulating CXCL10/CXCL8 Expression in High-Glucose Endothelial Cells by Sponging MicroRNAs. Indican 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 59-64 34688024-1 2021 The positron emitters (18F-Sodium Fluoride (NaF)) and X-rays used in Positron emission tomography (PET) combined with computed tomography (PET/CT) imaging have a high radiation dose, which results in a high patient dose. 18f-sodium fluoride 23-42 C-X-C motif chemokine ligand 8 Homo sapiens 44-47 34941711-7 2021 We discovered that lnc-SLC15A1-1 expression was significantly increased upon IS treatment in comparison with high glucose alone, and then cascaded the signal of chemokines CXCL10 and CXCL8 via sponging miR-27b, miR-297, and miR-150b. Glucose 114-121 C-X-C motif chemokine ligand 8 Homo sapiens 183-188 34175752-2 2021 The LiCl, NaOH, and NaF salts are used as the source of Li+ and Na+ ions in the LDI of the dipeptides. Dipeptides 91-101 C-X-C motif chemokine ligand 8 Homo sapiens 20-23 34175752-4 2021 The characteristic peak, related to (dipeptide-H + 2Na)+ species, is observed in the mass spectrum of Phe-Ala and Tyr-Ala dipeptides in the presence of NaF, while the breaking of the peptide bond (OC-NH) occurs for the Phe-Phe in the presence of the aforementioned salts. Dipeptides 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 34175752-4 2021 The characteristic peak, related to (dipeptide-H + 2Na)+ species, is observed in the mass spectrum of Phe-Ala and Tyr-Ala dipeptides in the presence of NaF, while the breaking of the peptide bond (OC-NH) occurs for the Phe-Phe in the presence of the aforementioned salts. 2-NAPHTHALENEMETHANOL 51-54 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 34175752-4 2021 The characteristic peak, related to (dipeptide-H + 2Na)+ species, is observed in the mass spectrum of Phe-Ala and Tyr-Ala dipeptides in the presence of NaF, while the breaking of the peptide bond (OC-NH) occurs for the Phe-Phe in the presence of the aforementioned salts. Phenylalanine 102-105 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 34175752-4 2021 The characteristic peak, related to (dipeptide-H + 2Na)+ species, is observed in the mass spectrum of Phe-Ala and Tyr-Ala dipeptides in the presence of NaF, while the breaking of the peptide bond (OC-NH) occurs for the Phe-Phe in the presence of the aforementioned salts. Alanine 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 34175752-4 2021 The characteristic peak, related to (dipeptide-H + 2Na)+ species, is observed in the mass spectrum of Phe-Ala and Tyr-Ala dipeptides in the presence of NaF, while the breaking of the peptide bond (OC-NH) occurs for the Phe-Phe in the presence of the aforementioned salts. Tyr-Ala 114-121 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 34175752-4 2021 The characteristic peak, related to (dipeptide-H + 2Na)+ species, is observed in the mass spectrum of Phe-Ala and Tyr-Ala dipeptides in the presence of NaF, while the breaking of the peptide bond (OC-NH) occurs for the Phe-Phe in the presence of the aforementioned salts. Dipeptides 122-132 C-X-C motif chemokine ligand 8 Homo sapiens 152-155 34175752-6 2021 The mass spectra of the dipeptides, recorded in the presence of LiCl, are crowded compared to those recorded in the presence of NaF and NaOH showing the effect of the type of alkali salt on the dipeptide fragmentation. Dipeptides 194-203 C-X-C motif chemokine ligand 8 Homo sapiens 128-131 34885572-2 2021 The electrical conductivity of molten cryolite mixtures NaF-AlF3-CaF2-Al2O3 with cryolite ratio (CR) of 2.1-3.0 and content of CaF2 and Al2O3, up to 8 wt%, was measured at the temperatures from liquidus to 1300 K. Based on the experimental results, a multifunctional equation for the electrical conductivity of oxide-fluoride cryolite melts was evaluated. aluminum fluoride 60-64 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 34885572-2 2021 The electrical conductivity of molten cryolite mixtures NaF-AlF3-CaF2-Al2O3 with cryolite ratio (CR) of 2.1-3.0 and content of CaF2 and Al2O3, up to 8 wt%, was measured at the temperatures from liquidus to 1300 K. Based on the experimental results, a multifunctional equation for the electrical conductivity of oxide-fluoride cryolite melts was evaluated. Oxides 311-316 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 34885572-2 2021 The electrical conductivity of molten cryolite mixtures NaF-AlF3-CaF2-Al2O3 with cryolite ratio (CR) of 2.1-3.0 and content of CaF2 and Al2O3, up to 8 wt%, was measured at the temperatures from liquidus to 1300 K. Based on the experimental results, a multifunctional equation for the electrical conductivity of oxide-fluoride cryolite melts was evaluated. Fluorides 317-325 C-X-C motif chemokine ligand 8 Homo sapiens 56-59 34885572-5 2021 The activation energy of electrical conductivity for molten NaF-AlF3 mixtures with CR 3.0 and 2.1, determined by the most mobile cations Na+, increased from 15.8 kJ/mol up to 18.5 kJ/mol. aluminum fluoride 64-68 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 34885572-5 2021 The activation energy of electrical conductivity for molten NaF-AlF3 mixtures with CR 3.0 and 2.1, determined by the most mobile cations Na+, increased from 15.8 kJ/mol up to 18.5 kJ/mol. Chromium 83-85 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 34885572-7 2021 Based on the ratio of the activation energies of the electrical conductivity and the viscous flow, the correlation between the electrical conductivity and viscosity of molten cryolite mixtures NaF-AlF3-CaF2-Al2O3 was illustrated. cryolite 175-183 C-X-C motif chemokine ligand 8 Homo sapiens 193-196 34876290-8 2022 Interleukin-8 was upregulated after leptin and dimethyl itaconate treatment at 6 hours (FC 26.35 at D4, P <= .001, and FC 23.26 at D3, P = .006). dimethyl itaconate 47-65 C-X-C motif chemokine ligand 8 Homo sapiens 0-13 34180760-15 2021 This study provides a theoretical basis for elucidating the mechanism of mepivacaine-induced nerve cell damage, and overexpressed miR-183-5p likely become a novel strategy to combat mepivacaine-induced nerve damage.Abbreviations:miRNA: Micro RNA; PDCD4: Programmed Cell Death 4; MDA: Malondialdehyde; SOD: Superoxide Dismutase; ROS: Reactive Oxygen Species; WT: Wild Type; Mut: Mutant; UTR: Untranslated Region; IL-6: Interleukin-6; IL-1beta: Interleukin-1beta; TNF-alpha: Tumor Necrosis Factor-alpha; IL-8: Interleukin-8; COX-2: Cyclooxygenase-2; iNOS: inducible NOS; MEP: Mepivacaine. mir-183-5p 130-140 C-X-C motif chemokine ligand 8 Homo sapiens 502-506 34560176-10 2021 Also, our results strongly suggested that BF4 also inhibits the endogenous cellular PC1/3 activity in Caco-2 cells, since PC1/3 inhibition by BF4 causes a large increase in IL-8 and IL-1beta secretion in Caco-2 cells. fluoroboric acid 142-145 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 34560176-10 2021 Also, our results strongly suggested that BF4 also inhibits the endogenous cellular PC1/3 activity in Caco-2 cells, since PC1/3 inhibition by BF4 causes a large increase in IL-8 and IL-1beta secretion in Caco-2 cells. fluoroboric acid 42-45 C-X-C motif chemokine ligand 8 Homo sapiens 173-177 34180760-15 2021 This study provides a theoretical basis for elucidating the mechanism of mepivacaine-induced nerve cell damage, and overexpressed miR-183-5p likely become a novel strategy to combat mepivacaine-induced nerve damage.Abbreviations:miRNA: Micro RNA; PDCD4: Programmed Cell Death 4; MDA: Malondialdehyde; SOD: Superoxide Dismutase; ROS: Reactive Oxygen Species; WT: Wild Type; Mut: Mutant; UTR: Untranslated Region; IL-6: Interleukin-6; IL-1beta: Interleukin-1beta; TNF-alpha: Tumor Necrosis Factor-alpha; IL-8: Interleukin-8; COX-2: Cyclooxygenase-2; iNOS: inducible NOS; MEP: Mepivacaine. mir-183-5p 130-140 C-X-C motif chemokine ligand 8 Homo sapiens 508-521 34506261-8 2021 Argon increased the proliferation of cardiomyocytes induced by OGD, decreased the release of LDH in cell culture medium, increased miR-21 expression in cells, decreased the expression of miR-21 target proteins PDCD4 and PTEN, decreased the levels of inflammatory factors (interleukin-1beta (IL-1beta), interleukin-6 (IL-6), and interleukin-8 (IL-8)) and oxidative stress factors (ROS and MDA), increased the SOD content, and decreased the cell apoptosis rate. Argon 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 328-341 34402375-6 2021 Firstly, we found that Tamsulosin reduced high glucose-induced expressions of TNF-alpha, IL-6, and IL-8. Tamsulosin 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 34402375-6 2021 Firstly, we found that Tamsulosin reduced high glucose-induced expressions of TNF-alpha, IL-6, and IL-8. Glucose 47-54 C-X-C motif chemokine ligand 8 Homo sapiens 99-103 34308769-8 2021 At the same time, sulforaphane weakened the ability of LPS to induce production of inflammatory cytokines (IL-1beta, IL-6, IL-8 and TNF-alpha) and the pro-apoptotic caspases-3 and -9. sulforaphane 18-30 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 34506261-8 2021 Argon increased the proliferation of cardiomyocytes induced by OGD, decreased the release of LDH in cell culture medium, increased miR-21 expression in cells, decreased the expression of miR-21 target proteins PDCD4 and PTEN, decreased the levels of inflammatory factors (interleukin-1beta (IL-1beta), interleukin-6 (IL-6), and interleukin-8 (IL-8)) and oxidative stress factors (ROS and MDA), increased the SOD content, and decreased the cell apoptosis rate. Argon 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 343-347 34847866-0 2021 pERK-mediated IL8 secretion can enhance the migration, invasion, and cisplatin resistance of CD10-positive oral cancer cells. Cisplatin 69-78 C-X-C motif chemokine ligand 8 Homo sapiens 14-17 34847866-4 2021 We hypothesized that IL8 might regulate migration, invasion, and cisplatin resistance of CD10-positive oral cancer cells through the ERK pathway. Cisplatin 65-74 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 34847866-11 2021 IL8 secreted by CD10H HN6 promoted migration and invasion and restored tumor chemosensitivity via the p-ERK signaling pathway, while the inhibition of IL8 increased the chemosensitivity to cisplatin. Cisplatin 189-198 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 34847866-11 2021 IL8 secreted by CD10H HN6 promoted migration and invasion and restored tumor chemosensitivity via the p-ERK signaling pathway, while the inhibition of IL8 increased the chemosensitivity to cisplatin. Cisplatin 189-198 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 34847866-12 2021 CONCLUSIONS: IL8 secretion by CD10 positive cells promotes migration, invasion, and cisplatin resistance of OSCC via the p-ERK signaling pathway. Cisplatin 84-93 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 34670781-8 2021 Accordingly, ectopic expression of CXCL8 in ALKBH5-deficient GBM cells partially restored TAM recruitment and tumor progression. tam 90-93 C-X-C motif chemokine ligand 8 Homo sapiens 35-40 34459104-8 2021 Treatment of HFLS-RA cells with OMTH prevented TNF-alpha mediated elevation of IL-1beta, IL-6 and IL-8. omth 32-36 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 34643021-4 2021 Moreover, we demonstrated, for the first time in human adipocytes, that cells exposure to PA induced gene expression of proinflammatory cytokines TNF-alpha, IL-6, IL-8, and MCP-1. Palmitic Acid 90-92 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 34851004-0 2022 Sulfation pattern dependent Iron (III) mediated interleukin-8 glycan binding. Iron 28-32 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 34851004-0 2022 Sulfation pattern dependent Iron (III) mediated interleukin-8 glycan binding. Polysaccharides 62-68 C-X-C motif chemokine ligand 8 Homo sapiens 48-61 34851004-1 2022 Cytokines such as interleukin-8 activate the immune system during infection and interact with sulfated glycosaminoglycans with specific sulfation patterns. Glycosaminoglycans 103-121 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 34851004-3 2022 We evaluated the effect of both hyaluronan sulfation pattern and Fe3+ on interleukin-8 binding by electrochemical impedance spectroscopy and surface characterizations. Hyaluronic Acid 32-42 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 34851004-3 2022 We evaluated the effect of both hyaluronan sulfation pattern and Fe3+ on interleukin-8 binding by electrochemical impedance spectroscopy and surface characterizations. ferric sulfate 65-69 C-X-C motif chemokine ligand 8 Homo sapiens 73-86 34083105-0 2021 Corrigendum to "IL-8 negatively regulates ABCA1 expression and cholesterol efflux via upregulating miR-183 in THP-1 macrophage-derived foam cells" (Cytokine 122 (2019) 154385). Cholesterol 63-74 C-X-C motif chemokine ligand 8 Homo sapiens 16-20 34626802-5 2021 The IFNgamma-induced IL-8 expression is dependent on JAK1, STAT1, and p65 NFkappaB, and is associated with an increased occupancy of K314/315 acetylated p65 NFkappaB and Ser-727 phosphorylated STAT1 at the IL-8 promoter. Serine 170-173 C-X-C motif chemokine ligand 8 Homo sapiens 21-25 34308659-5 2021 Methyl mercury treatment significantly induced the adhesion of monocyte to HMEC-1 endothelial cells, a critical step in atherosclerosis, while also upregulating the expression of proinflammatory cytokines interleukin-6, interleukin-8. methyl mercury 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 220-233 34780879-6 2021 Fluoride reduced mitochondrial antioxidant enzyme activities and SOD2 acetylation by downregulating Sirt3 expression in the brains of mice and NaF-treated SH-SY5Y cells. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 143-146 34780879-7 2021 Moreover, fluoride lowered mtDNA transcription and induced mitochondrial dysfunction along with increased FoxO3A acetylation in the brains of mice and NaF-treated SH-SY5Y cells. Fluorides 10-18 C-X-C motif chemokine ligand 8 Homo sapiens 151-154 34636179-11 2021 Interleukin-6 (IL-6) and IL-8 production by stimulated ECs were unaltered by incubation with macrolides, whereas Clarithromycin exposure significantly decreased IL-6 gene expression. Clarithromycin 113-127 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 34153179-10 2021 However, ASA was inflammatory above its therapeutic window, increasing the levels of PGE2 and IL-8 above those seen with bradykinin stimulation alone. Aspirin 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 34607230-8 2021 Besides, in patients, receiving lovastatin the CRP, IL-6, IL-8 levels were significantly decreased from T1 to T3 than to the control group. Lovastatin 32-42 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 34626802-5 2021 The IFNgamma-induced IL-8 expression is dependent on JAK1, STAT1, and p65 NFkappaB, and is associated with an increased occupancy of K314/315 acetylated p65 NFkappaB and Ser-727 phosphorylated STAT1 at the IL-8 promoter. Serine 170-173 C-X-C motif chemokine ligand 8 Homo sapiens 206-210 34950767-4 2021 Using the human keratinocyte-derived cell line HaCaT, the present in vitro studies indicate that pretreatment of HaCaT keratinocytes with PAFR agonist ester can synergize with low fluences of UVB to generate high levels of MVP as well as IL-8 protein. Esters 151-156 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 34019775-6 2021 CoCl2 caused an increase of IL-8 in HaCaT cells, while the induction of also IL-13 and IL-1beta was observed in THP-1 cells and co-cultures. cobaltous chloride 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 28-32 34879788-4 2021 Generalized estimating equation was used to evaluate the association between exposure to PM2.5 and NO2 and the following serum cytokine levels on the 7 days preceding clinical assessment and serum collection: MCP1, IL-6, IL-8, IL-10, IL-17, IFN-alpha, and TNF-alpha. pm2.5 89-94 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 34879788-4 2021 Generalized estimating equation was used to evaluate the association between exposure to PM2.5 and NO2 and the following serum cytokine levels on the 7 days preceding clinical assessment and serum collection: MCP1, IL-6, IL-8, IL-10, IL-17, IFN-alpha, and TNF-alpha. Nitrogen Dioxide 99-102 C-X-C motif chemokine ligand 8 Homo sapiens 221-225 34798932-4 2021 The pro-inflammatory response in terms of IL-8 expression was strongest in cells exposed to Bentonite, whereas surface modification resulted in decreased toxicity in both cell lines when exposed to Nanofil9 and NanofilSE3000. Bentonite 92-101 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 34666245-6 2021 Here, we show that Trelagliptin mitigates IL-1beta-induced production of inflammatory cytokines such as interleukin 6 (IL-6), interleukin 8 (IL-8), and tumor necrosis factor-alpha (TNF-alpha) in human chondrocytes. trelagliptin 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 126-139 34666245-6 2021 Here, we show that Trelagliptin mitigates IL-1beta-induced production of inflammatory cytokines such as interleukin 6 (IL-6), interleukin 8 (IL-8), and tumor necrosis factor-alpha (TNF-alpha) in human chondrocytes. trelagliptin 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 34856488-5 2021 The results showed that endosulfan significantly promoted cell proliferation, accompanied with the decrease of p27 mRNA expression and the increase in the mRNA expression levels of p21 and inflammatory factors IL-6/IL-8. Endosulfan 24-34 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 34624807-9 2021 CONCLUSION: This systematic review broadly reports that, in contrast to other classes of phytochemicals, flavonoids have the greatest therapeutic potential against arthritis by modulating the expression of pro-inflammatory TNF-alpha, IL-1beta, IL-6, IL-8, and IL-17, as well as anti-inflammatory IL-2 and IL-10 cytokines, through the suppression of dynamic inflammatory biomarkers. Flavonoids 105-115 C-X-C motif chemokine ligand 8 Homo sapiens 250-254 34941643-1 2021 This report describes the significance of the kinetic parameters (k-values) obtained from the analysis of dynamic positron emission tomography (PET) scans using the Hawkins model describing the pharmacokinetics of sodium fluoride ((18F)NaF) to understand bone physiology. Sodium Fluoride 214-229 C-X-C motif chemokine ligand 8 Homo sapiens 236-239 34697842-3 2021 Results of ELISA experiments revealed that Garcinia kola extract (6.25, 12.5, and 25 mug/ml) and garcinoic acid (1.25, 2.5, and 5 muM) significantly reduced SARS-CoV-2 spike protein S1-induced secretion of TNFalpha, IL-6, IL-1beta, and IL-8 in PBMCs. garcinoic acid 97-111 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 34933727-9 2021 Other pivotal features of melatonin are its anti-inflammatory properties, which decrease pro-inflammatory cytokines expression and factors such as IL-8, IL-6, and TNF. Melatonin 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 34943473-3 2021 In addition, recent studies have suggested that microcalcification revealed by 18F-sodium fluoride (NaF) may be more sensitive at detecting atherogenic changes compared to FDG-PET. 18f-sodium fluoride 79-98 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 34880922-6 2021 Noscapine can reduce endothelial cell migration in the brain by inhibiting endothelial cell activator interleukin 8 (IL-8). Noscapine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 102-115 34880922-6 2021 Noscapine can reduce endothelial cell migration in the brain by inhibiting endothelial cell activator interleukin 8 (IL-8). Noscapine 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 117-121 34885115-15 2021 CAFs derived from Osimertinib-resistant cells secreted more IL-6, IL-8, and hepatocyte growth factor (HGF), expressed stronger CAF markers including alpha-smooth muscle actin (alpha-SMA), fibroblast activation protein (FAP) plus platelet-derived growth factor receptor (PDGFR), and enhanced stemness and Osimertinib resistance in NSCLC cells. osimertinib 18-29 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 34943005-6 2021 Using ELISA, we demonstrate that the disulfide bridge between the enzymatic cysteines is required to allow improved TLR4-dependent IL-8 secretion. Disulfides 37-46 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 34943005-6 2021 Using ELISA, we demonstrate that the disulfide bridge between the enzymatic cysteines is required to allow improved TLR4-dependent IL-8 secretion. Cysteine 76-85 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 34826187-9 2022 Taken together, these observations suggest that SIRT1 stabilized through phosphorylation on serine 27 exerts oncogenic effects at least partly through deacetylation-dependent activation of Snail and subsequent transcription of IL-6 and IL-8 in human colon cancer cells. Serine 92-98 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 34884486-11 2021 Preincubation with heparin, autotaxin (ATX) inhibitor HA130 or lysophosphatidic acid (LPA) receptor antagonist Ki16425 reduced PLA1A-induced-secretion of IL-8. Heparin 19-26 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 34886097-7 2021 In addition, both SK-119 and SH-29 were able to reduce DPM-induced IL-8 hypersecretion in pharmacologically relevant concentrations. sk-119 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 34886097-7 2021 In addition, both SK-119 and SH-29 were able to reduce DPM-induced IL-8 hypersecretion in pharmacologically relevant concentrations. sh-29 29-34 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 34886097-7 2021 In addition, both SK-119 and SH-29 were able to reduce DPM-induced IL-8 hypersecretion in pharmacologically relevant concentrations. dpm 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 34884486-11 2021 Preincubation with heparin, autotaxin (ATX) inhibitor HA130 or lysophosphatidic acid (LPA) receptor antagonist Ki16425 reduced PLA1A-induced-secretion of IL-8. HA130 54-59 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 34884486-11 2021 Preincubation with heparin, autotaxin (ATX) inhibitor HA130 or lysophosphatidic acid (LPA) receptor antagonist Ki16425 reduced PLA1A-induced-secretion of IL-8. lysophosphatidic acid 63-84 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 34884486-11 2021 Preincubation with heparin, autotaxin (ATX) inhibitor HA130 or lysophosphatidic acid (LPA) receptor antagonist Ki16425 reduced PLA1A-induced-secretion of IL-8. lysophosphatidic acid 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 34884486-11 2021 Preincubation with heparin, autotaxin (ATX) inhibitor HA130 or lysophosphatidic acid (LPA) receptor antagonist Ki16425 reduced PLA1A-induced-secretion of IL-8. 3-(4-(4-((1-(2-chlorophenyl)ethoxy)carbonyl amino)-3-methyl-5-isoxazolyl) benzylsulfanyl) propanoic acid 111-118 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 34582847-5 2021 LPC stimulation resulted in elevated secretion of interleukin (IL)-6 and IL-8 in HUVECs, accompanied with the activation of ER stress and NF-kappaB pathway. lpc 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 73-77 34834886-13 2021 In addition, magnolol displayed inhibitory effects towards IL-1beta, IL-8 and TNF-alpha released from lipopolysaccharide (LPS)-stimulated human neutrophils, while honokiol only decreased IL-1beta secretion, compared to the untreated control. magnolol 13-21 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 34869555-9 2021 Results: Compared with the fasting group, the CHO group exhibited a decrease in interleukin 6 (IL-6) levels on days 1 and 7 (75.47 and 7.06 pg/mL, respectively), IL-8 levels on day 1 (274.61 pg/mL) and tumour necrosis factor (TNF) levels on days 1, 3, and 7 (11.16, 9.55, and 9.67 pg/mL, respectively). CAV protocol 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 34869555-13 2021 Conclusion: Preoperative CHO and drinking water are associated with decreased levels of IL-6, IL-8, and TNF. CAV protocol 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 34869555-13 2021 Conclusion: Preoperative CHO and drinking water are associated with decreased levels of IL-6, IL-8, and TNF. Water 42-47 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 34833991-12 2021 Finally, the pro-inflammatory cytokines (IL-1beta, IL-6, and IL-8) released by PBMCs triggered by SARS-CoV-2 were decreased after treatment with curcumin. Curcumin 145-153 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 34799554-4 2021 ADT induced the secretion of WNT4 which upon engagement of TCF7L1 in prostate cancer cells, enhanced IL-8 and CXCR2 expressions. adt 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 101-105 34816902-2 2021 This study aimed to compare the effects of conventional (sodium fluoride (NaF)) and stannous fluoride (SnF2)-containing dentifrices on reducing erosive tooth wear (ETW). Sodium Fluoride 57-72 C-X-C motif chemokine ligand 8 Homo sapiens 74-77 34732192-0 2021 Nicotine regulates autophagy of human periodontal ligament cells through alpha7 nAchR that promotes secretion of inflammatory factors IL-1beta and IL-8. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 34785925-8 2021 Furthermore, blocking Stat3 signaling pathway by treatment with TSA and/or small molecule compound Stattic of an p-Stat3 inhibitor effectively abrogated LPS-induced tumorosphere forming with decrease of IL-6, IL-8 and stemness biomarkers CD44, SOX-2 expression. trichostatin A 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 209-213 34785925-10 2021 TSA could prevent, at least in part, the LPS-induced malignant transformation by targeting p-Stat3/c-Myc signaling pathway and reducing inflammatory IL-6, IL-8. trichostatin A 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 34769415-6 2021 In addition, pretreatment with naringenin might inhibit the secretion of TNF-alpha, IL-6, and IL-8, as well as the proteins cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) via the suppression of NF-kappaB and mitogen-activated protein kinase (MAPK) signaling in ethanol-stimulated stomach epithelial KATO III cells. naringenin 31-41 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 34668373-9 2021 The significant increase in endocytosed Ta-Au resulted in a 20% decrease in viability, and a 4-fold increase in IL-8 cytokine secretion when cultured on soft PU SDCs at ALI. ta-au 40-45 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 34732192-3 2021 To investigated the mechanism through which nicotine regulates autophagy of human periodontal ligament cells (hPDLCs) through the alpha7 nicotinic acetylcholine receptor (alpha7 nAChR) and how autophagy further regulates the release of IL-1beta and IL-8 secretion in hPDLCs. Nicotine 44-52 C-X-C motif chemokine ligand 8 Homo sapiens 249-253 34732192-7 2021 RT-qPCR and ELISA results revealed a noticeable rise in the release of inflammatory factors IL-1beta and IL-8 from hPDLCs in response to nicotine. Nicotine 137-145 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 34732192-8 2021 RT-qPCR and ELISA results showed that nicotine can significantly up-regulate the release of inflammatory factors IL-1beta and IL-8 in hPDLCs, and this effect can be inhibited by 3-MA (p < 0.05). Nicotine 38-46 C-X-C motif chemokine ligand 8 Homo sapiens 126-130 34726293-9 2022 RESULTS AND DISCUSSION: After 12 weeks, the ethosuximide group showed a statistically and significantly greater reduction in the serum levels of TNF-alpha, IL-6, IL-8, faecal myeloperoxidase and faecal NGAL in comparison with the control group after the treatment. Ethosuximide 44-56 C-X-C motif chemokine ligand 8 Homo sapiens 162-166 34795863-6 2021 A subsequent functional assay using the MDA-MB-231 cell line demonstrated that the d-galactal-benzimidazole hybrid and the analogous galactoside derivative reduced the secretion of the proinflammatory cytokines interleukin-6 (IL-6) and IL-8 in a dose-dependent manner. d-galactal-benzimidazole 83-107 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 34795863-6 2021 A subsequent functional assay using the MDA-MB-231 cell line demonstrated that the d-galactal-benzimidazole hybrid and the analogous galactoside derivative reduced the secretion of the proinflammatory cytokines interleukin-6 (IL-6) and IL-8 in a dose-dependent manner. Galactosides 133-144 C-X-C motif chemokine ligand 8 Homo sapiens 236-240 34539828-4 2021 ALA/DHLA reduce the levels of pro-inflammatory cytokines (IL-1beta, IL-6, IL-8 and IL-17), while increasing the secretion of anti-inflammatory cytokines (IL-10). Thioctic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 34126877-8 2021 O3-induced pro-inflammatory gene expression for CXCL2 and CXCL8/IL8 was further enhanced in NLRP2 knockout cells, suggesting a negative regulatory role. Ozone 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 58-63 34126877-8 2021 O3-induced pro-inflammatory gene expression for CXCL2 and CXCL8/IL8 was further enhanced in NLRP2 knockout cells, suggesting a negative regulatory role. Ozone 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 64-67 34126877-9 2021 Reconstitution of NLRP2 KO cells with K1019R mutant NLRP2 partially blocked SecoA adduction and enhanced O3-induced IL-8 release as compared to wild type NLRP2. Ozone 105-107 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 34601318-1 2021 OBJECTIVE: Sodium fluoride (NaF) plays an important role in preventing dental caries. Sodium Fluoride 11-26 C-X-C motif chemokine ligand 8 Homo sapiens 28-31 34310083-11 2021 Azithromycin concentration was positively correlated with IL-8 (r = 0.38, p = 0.03), IL1a (r = 0.39, p = 0.03), and IL-1b (r = 0.36, p = 0.04) in amniotic fluid. Azithromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 58-62 34499917-8 2021 Hcy exposure increased CBS protein expression, hydrogen sulfide levels and pro-inflammatory cytokines, modulating CBS by silencing did not alter H2S levels, but inhibition of CSE with PAG inhibited H2S production and decreased cytokine (IL-6 and IL-8) levels. Homocysteine 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 246-250 34837919-12 2021 A significant decrease in NAF was also observed in Temozolomide (p < 0.05) and Opuntiol (p < 0.05) treated cells. Temozolomide 51-63 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 34837919-12 2021 A significant decrease in NAF was also observed in Temozolomide (p < 0.05) and Opuntiol (p < 0.05) treated cells. opuntiol 79-87 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 34507119-4 2021 First, we evaluated the effect of lupeol (100 microM) on inflammatory response induced by lipopolysaccharide (LPS) in retinal pigment epithelium cells (ARPE-19) by measuring levels of released interleukins (IL-6 and IL-8). lupeol 34-40 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 34507119-8 2021 Treatment with lupeol (100 microM) significantly decreased IL-6 and IL-8 levels in comparison to untreated LPS-activated ARPE-19 cells. lupeol 15-21 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 34725321-12 2021 In addition, activation of the CXCL8 receptor CXCR1 during thapsigargin exposure supported subsequent sphere formation by cancer cells. Thapsigargin 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 31-36 34539828-4 2021 ALA/DHLA reduce the levels of pro-inflammatory cytokines (IL-1beta, IL-6, IL-8 and IL-17), while increasing the secretion of anti-inflammatory cytokines (IL-10). dihydrolipoic acid 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 34600651-7 2021 CB-B inhibited the release of cytokine IL-8, and both products were effective in restoring the TEER. cb-b 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 34609010-7 2021 Our results showed that berberine-LCNs significantly reduced the expression of CCl-20, CXCL-8 and HO-1 at dose of 5microM. Berberine 24-33 C-X-C motif chemokine ligand 8 Homo sapiens 87-93 34059950-8 2021 RESULTS: VEGF, MCP-1, IL-8, and IL-6 levels in the aqueous humor of patients with RVO-ME were significantly higher compared with control and were positively correlated with the CRTBT. rvo-me 82-88 C-X-C motif chemokine ligand 8 Homo sapiens 22-26 34059950-12 2021 CONCLUSION: VEGF, MCP-1, IL-8, and IL-6 levels were significantly increased in patients with RVO-ME and were positively correlated with ME. rvo-me 93-99 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 34609010-7 2021 Our results showed that berberine-LCNs significantly reduced the expression of CCl-20, CXCL-8 and HO-1 at dose of 5microM. lcns 34-38 C-X-C motif chemokine ligand 8 Homo sapiens 87-93 34609010-8 2021 Collectively, our findings suggest that berberine-LCNs have inhibitory effect on inflammation/oxidative stress related cytokines i.e. CCL20, CXCL-8, and HO-1 which could be a novel therapeutic target for the management of lung cancer. Berberine 40-49 C-X-C motif chemokine ligand 8 Homo sapiens 141-147 34609010-11 2021 Our study showed that Berberine LCNs significantly downregulate the expression of CXCL-8, CCL-20 and HO-1 which suggests that Berberine loaded nanoparticles could be a promising therapeutic alternative for the management of lung cancer. berberine lcns 22-36 C-X-C motif chemokine ligand 8 Homo sapiens 82-88 34609010-11 2021 Our study showed that Berberine LCNs significantly downregulate the expression of CXCL-8, CCL-20 and HO-1 which suggests that Berberine loaded nanoparticles could be a promising therapeutic alternative for the management of lung cancer. Berberine 126-135 C-X-C motif chemokine ligand 8 Homo sapiens 82-88 34438042-2 2021 Here we demonstrate that the hydrophobic bile acid, deoxycholic acid (DCA), stimulated the production of IL-6 and IL-8 mRNA and protein in Het-1A, a model of normal oesophageal cells. Bile Acids and Salts 41-50 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 34438042-2 2021 Here we demonstrate that the hydrophobic bile acid, deoxycholic acid (DCA), stimulated the production of IL-6 and IL-8 mRNA and protein in Het-1A, a model of normal oesophageal cells. Deoxycholic Acid 52-68 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 34438042-2 2021 Here we demonstrate that the hydrophobic bile acid, deoxycholic acid (DCA), stimulated the production of IL-6 and IL-8 mRNA and protein in Het-1A, a model of normal oesophageal cells. Deoxycholic Acid 70-73 C-X-C motif chemokine ligand 8 Homo sapiens 114-118 34438042-3 2021 DCA-induced production of IL-6 and IL-8 was attenuated by pharmacologic inhibition of the Protein Kinase C (PKC), MAP kinase, tyrosine kinase pathways, by the cholesterol sequestering agent, methyl-beta-cyclodextrin (MCD) and by the hydrophilic bile acid, ursodeoxycholic acid (UDCA). Deoxycholic Acid 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 35-39 34438042-4 2021 The cholesterol-interacting agent, nystatin, which binds cholesterol without removing it from the membrane, synergized with DCA to induce IL-6 and IL-8. Cholesterol 4-15 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 34628106-5 2021 In human placental tissue culture, treatment with BHB suppressed the secretion levels of inflammatory cytokines, such as interleukin (IL)-1beta, IL-6, and IL-8, but did not affect the mRNA expression levels of NLRP3 inflammasome-associated factors. 3-Hydroxybutyric Acid 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 34438042-4 2021 The cholesterol-interacting agent, nystatin, which binds cholesterol without removing it from the membrane, synergized with DCA to induce IL-6 and IL-8. Nystatin 35-43 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 34438042-4 2021 The cholesterol-interacting agent, nystatin, which binds cholesterol without removing it from the membrane, synergized with DCA to induce IL-6 and IL-8. Deoxycholic Acid 124-127 C-X-C motif chemokine ligand 8 Homo sapiens 147-151 34438042-7 2021 while knockdown of caveolin-1 expression using siRNA resulted in a decreased level of IL-8 production in response to DCA. Deoxycholic Acid 117-120 C-X-C motif chemokine ligand 8 Homo sapiens 86-90 34438042-8 2021 Taken together, these results demonstrate that DCA stimulates IL-6 and IL-8 production in oesophageal cells via lipid raft-associated signaling. Deoxycholic Acid 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 34771621-4 2021 In this study, we show that gemcitabine stimulates the expression of pro-inflammatory cytokines, such as IL6 and IL8, under the influence of the CD95/CD95L system and the pharmacological inhibitor, sCD95Fc, substantially reduced the expression in two PDAC cell lines, PancTuI-luc and A818-4. gemcitabine 28-39 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 34106437-5 2021 Progesterone stimulation decreased the expression of TLR2, TLR5, and Nod2 genes (alone and/or in combination with TLR/NLR agonists) and decreased the expression of IL-1beta and IL-8 genes increased by stimulation with specific agonists for TLR2, TLR4, TLR5, Nod1, and Nod2. Progesterone 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 34106437-6 2021 Moreover, progesterone decreased thrombin-induced IL-8 gene expression. Progesterone 10-22 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 34533029-3 2021 In our study, miR-10a-5p overexpression inhibited the proliferation, migration, and IL-6/IL-8 level of LX-2 and human liver cancer fibroblasts (HLCFs) cells. mir-10a-5p 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 89-93 34455857-3 2021 Methods: In a multicenter cross-sectional observational cohort study, patients with TAVI or bioprosthetic SAVR underwent baseline echocardiography, CT angiography and 18F-sodium fluoride (18F-NaF) positron emission tomography (PET). 18f-sodium fluoride 167-186 C-X-C motif chemokine ligand 8 Homo sapiens 192-195 34715784-5 2021 IL-6 and IL-8 as pro-inflammatory cytokines released during surgery, were lowered in mean 28-fold and 52-fold during the Catuvab procedure, respectively, whereas Catumaxomab antibody was detected in 8 of 16 of the final EC products at a considerable decreased and uncritical residual amount (37 ng in mean). catuvab 121-128 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 34835369-8 2021 Overexpression of the mouse macrophage inflammatory protein 2 mRNA in the colon as a functional homolog of human interleukin-8 was decreased by the orally administered EPS. eps 168-171 C-X-C motif chemokine ligand 8 Homo sapiens 113-126 34769627-7 2021 Naive THP-1 cells produced significantly elevated levels of IL-1beta, IL-8, and TNF-alpha when exposed to ethyl maltol and hexanal. ethyl maltol 106-118 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 34737896-8 2021 We found that pentosidine induced upregulation of CXCL2, IL8, and MMP12 mRNA expression (inflammatory and elastotic markers, respectively). pentosidine 14-25 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 34768873-8 2021 Graphene exposure (10 microg/mL) for 24 h significantly increased levels of pro-inflammatory cytokines IFNgamma, IL-8, IL-17, IL-6, IL-9, MIP-1alpha, and Eotaxin. Graphite 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 113-117 34769627-7 2021 Naive THP-1 cells produced significantly elevated levels of IL-1beta, IL-8, and TNF-alpha when exposed to ethyl maltol and hexanal. n-hexanal 123-130 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 34622888-5 2021 Based on MD simulations, we propose that the magnitude of cation excess (which is salt specific) depends on the ability of the electrolyte to perturb the water network at the DNA interface: In the NaF atmosphere, the ions reduce the strength of interactions between water and the DNA more than in case of a NaCl electrolyte. Salts 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 197-200 34622888-5 2021 Based on MD simulations, we propose that the magnitude of cation excess (which is salt specific) depends on the ability of the electrolyte to perturb the water network at the DNA interface: In the NaF atmosphere, the ions reduce the strength of interactions between water and the DNA more than in case of a NaCl electrolyte. Water 154-159 C-X-C motif chemokine ligand 8 Homo sapiens 197-200 34622888-5 2021 Based on MD simulations, we propose that the magnitude of cation excess (which is salt specific) depends on the ability of the electrolyte to perturb the water network at the DNA interface: In the NaF atmosphere, the ions reduce the strength of interactions between water and the DNA more than in case of a NaCl electrolyte. Water 266-271 C-X-C motif chemokine ligand 8 Homo sapiens 197-200 34666750-10 2021 LABA/GCS attenuation of Poly I:C or imiquimod-induced IL-6 and IL-8 were potentiated with ABCC4 and PDE4 inhibition, which was greater when ABCC4 and PDE4 inhibition was combined. Imiquimod 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 34666758-12 2021 TNF-alpha or flagellin-induced IL-8 levels were also significantly reduced with SC79 treatment. SC79 80-84 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 34666750-10 2021 LABA/GCS attenuation of Poly I:C or imiquimod-induced IL-6 and IL-8 were potentiated with ABCC4 and PDE4 inhibition, which was greater when ABCC4 and PDE4 inhibition was combined. Poly I 24-30 C-X-C motif chemokine ligand 8 Homo sapiens 63-67 34590836-7 2021 Also, we found that AZ3451 attenuated ox-LDL-induced expression and production of pro-inflammatory cytokines such as interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-alpha), and interleukin-8 (IL-8). AZ3451 20-26 C-X-C motif chemokine ligand 8 Homo sapiens 184-197 34590836-7 2021 Also, we found that AZ3451 attenuated ox-LDL-induced expression and production of pro-inflammatory cytokines such as interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-alpha), and interleukin-8 (IL-8). AZ3451 20-26 C-X-C motif chemokine ligand 8 Homo sapiens 199-203 34733807-8 2021 The univariate analysis showed that there were significant differences between the PB group and the non-PB group in LDH, D-dimer, CD3+CD4+(%), CD3+CD4+/CD3+CD8+, CD3 count, CD4 count, CD8 count, complement 3, IL8, IL-1beta, IL-2, IL-10 (P < 0.05). pladienolide B 83-85 C-X-C motif chemokine ligand 8 Homo sapiens 209-212 34733276-8 2021 In vitro treatment of PBMCs from either SLE patients or healthy controls with 17beta-estradiol at physiological concentration (~50 pg/ml) also significantly increased secretion of many pro-inflammatory cytokines and chemokines (IL-6, IL-12, IL-17, IL-8, IFN-gamma; MIP1alpha, and MIP1beta) in both groups. Estradiol 78-94 C-X-C motif chemokine ligand 8 Homo sapiens 248-252 34655103-11 2022 LPS exposure evoked viability reduction, increased LDH release and apoptosis, and induced production of inflammatory cytokines (IL-6, IL-8, and MCP-1) and MUC5AC hypersecretion in human AECs, which were alleviated by euxanthone. euxanthone 217-227 C-X-C motif chemokine ligand 8 Homo sapiens 134-138 34681839-2 2021 Gold standard therapy temozolomide (TMZ) is known to induce upregulation of IL8/CXCL2/CXCR2 signaling that promotes tumor progression and angiogenesis. Temozolomide 22-34 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 34681839-2 2021 Gold standard therapy temozolomide (TMZ) is known to induce upregulation of IL8/CXCL2/CXCR2 signaling that promotes tumor progression and angiogenesis. Temozolomide 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 76-79 34754605-3 2021 During the past decade, numerous papers have described a major role for sodium 18F-fluoride (NaF) as another tracer for assessing this vascular disease. SODIUM FLUORIDE F-18 72-91 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 34425162-4 2021 Pretreatment of HNE cells with the specific vacuolar H+-ATPase inhibitor bafilomycin A1 reduced the RV-C03 RNA levels in the ASL; inflammatory cytokines, including interleukin (IL)-1beta, IL-6 and IL-8, in the supernatant; the mRNA expression of the RV-C receptor cadherin-related family member 3 (CDHR3) in the cells; and the number of acidic endosomes where RV-B RNA enters the cytoplasm. bafilomycin A1 73-87 C-X-C motif chemokine ligand 8 Homo sapiens 197-201 34659651-0 2021 18F-Sodium Fluoride (NaF) Uptake in Calcified Bladder Carcinoma: Double Density Sign 18F-Sodium fluoride (NaF) is primarily a skeletal imaging agent which can be localized in extraosseous calcified foci. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 34659651-0 2021 18F-Sodium Fluoride (NaF) Uptake in Calcified Bladder Carcinoma: Double Density Sign 18F-Sodium fluoride (NaF) is primarily a skeletal imaging agent which can be localized in extraosseous calcified foci. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 34659651-0 2021 18F-Sodium Fluoride (NaF) Uptake in Calcified Bladder Carcinoma: Double Density Sign 18F-Sodium fluoride (NaF) is primarily a skeletal imaging agent which can be localized in extraosseous calcified foci. 18f-sodium fluoride 85-104 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 34659651-0 2021 18F-Sodium Fluoride (NaF) Uptake in Calcified Bladder Carcinoma: Double Density Sign 18F-Sodium fluoride (NaF) is primarily a skeletal imaging agent which can be localized in extraosseous calcified foci. 18f-sodium fluoride 85-104 C-X-C motif chemokine ligand 8 Homo sapiens 106-109 34672097-8 2022 The expression of IL8 gene was reduced by all applied concentrations of ClO2 . Chlorous acid 72-76 C-X-C motif chemokine ligand 8 Homo sapiens 18-21 34601878-9 2021 This result is explained by different interactions of each salt with the micelle: whereas NaF interacts primarily with PEO chains, NaCl may also partition to the PPO/PEO interface in low levels, increasing micelle surface tension, scission energy, and contour length. Salts 59-63 C-X-C motif chemokine ligand 8 Homo sapiens 90-93 34754406-15 2021 Severity of mucosal inflammatory changes is proportional to luminal (NO), which might be tied to IL-8 production. Phenobarbital 60-67 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 34643794-14 2022 In addition, bevacizumab reduced the secretion of IL-8 and TNFalpha after Poly I:C stimulation at selected time points. Poly I-C 74-82 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 34690806-10 2021 Transfection with small interfering RNA (siRNA) targeting STIM1 and pretreatment with NAC alleviated CSE-induced increase in intracellular Ca2+ levels and IL-8 expression. Acetylcysteine 86-89 C-X-C motif chemokine ligand 8 Homo sapiens 155-159 34637509-9 2022 Specific fatty acids including 14:0 and long chain n-6 fatty acids being negatively and positively, respectively, associated with IL-8 were also found to be positively associated with SAA. Fatty Acids 9-20 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 34637509-9 2022 Specific fatty acids including 14:0 and long chain n-6 fatty acids being negatively and positively, respectively, associated with IL-8 were also found to be positively associated with SAA. Fatty Acids, Omega-6 51-66 C-X-C motif chemokine ligand 8 Homo sapiens 130-134 34690806-0 2021 Cigarette Smoke Promotes Interleukin-8 Production in Alveolar Macrophages Through the Reactive Oxygen Species/Stromal Interaction Molecule 1/Ca2+ Axis. Oxygen 95-101 C-X-C motif chemokine ligand 8 Homo sapiens 25-38 34690806-4 2021 Our results showed that the reactive oxygen species (ROS)/STIM1/Ca2+ axis played a critical role in CS-induced secretion of interleukin (IL)-8 in human alveolar macrophages. Reactive Oxygen Species 28-51 C-X-C motif chemokine ligand 8 Homo sapiens 124-142 34680563-7 2021 L-HCV promotes cell growth and alters cell adhesion and chemokine signaling via CXCL8-mediated-SRC regulation. l-hcv 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 34625847-9 2022 The average interleukin-8 (IL-8) concentrations were significantly lower in the fluorometholone (4.80 pg/mL), ketorolac tromethamine (4.84 pg/mL), and fluorometholone + ketorolac tromethamine (4.68 pg/mL) groups than in the control group (6.83 pg/mL). Fluorometholone 80-95 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 34625847-9 2022 The average interleukin-8 (IL-8) concentrations were significantly lower in the fluorometholone (4.80 pg/mL), ketorolac tromethamine (4.84 pg/mL), and fluorometholone + ketorolac tromethamine (4.68 pg/mL) groups than in the control group (6.83 pg/mL). Fluorometholone 80-95 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 34625847-9 2022 The average interleukin-8 (IL-8) concentrations were significantly lower in the fluorometholone (4.80 pg/mL), ketorolac tromethamine (4.84 pg/mL), and fluorometholone + ketorolac tromethamine (4.68 pg/mL) groups than in the control group (6.83 pg/mL). Ketorolac Tromethamine 110-132 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 34625847-9 2022 The average interleukin-8 (IL-8) concentrations were significantly lower in the fluorometholone (4.80 pg/mL), ketorolac tromethamine (4.84 pg/mL), and fluorometholone + ketorolac tromethamine (4.68 pg/mL) groups than in the control group (6.83 pg/mL). Ketorolac Tromethamine 110-132 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 34625847-9 2022 The average interleukin-8 (IL-8) concentrations were significantly lower in the fluorometholone (4.80 pg/mL), ketorolac tromethamine (4.84 pg/mL), and fluorometholone + ketorolac tromethamine (4.68 pg/mL) groups than in the control group (6.83 pg/mL). Fluorometholone 151-166 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 34625847-9 2022 The average interleukin-8 (IL-8) concentrations were significantly lower in the fluorometholone (4.80 pg/mL), ketorolac tromethamine (4.84 pg/mL), and fluorometholone + ketorolac tromethamine (4.68 pg/mL) groups than in the control group (6.83 pg/mL). Fluorometholone 151-166 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 34625847-9 2022 The average interleukin-8 (IL-8) concentrations were significantly lower in the fluorometholone (4.80 pg/mL), ketorolac tromethamine (4.84 pg/mL), and fluorometholone + ketorolac tromethamine (4.68 pg/mL) groups than in the control group (6.83 pg/mL). Ketorolac Tromethamine 169-191 C-X-C motif chemokine ligand 8 Homo sapiens 12-25 34625847-9 2022 The average interleukin-8 (IL-8) concentrations were significantly lower in the fluorometholone (4.80 pg/mL), ketorolac tromethamine (4.84 pg/mL), and fluorometholone + ketorolac tromethamine (4.68 pg/mL) groups than in the control group (6.83 pg/mL). Ketorolac Tromethamine 169-191 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 34625847-11 2022 CONCLUSION: Preoperative fluorometholone instillation reduced IL-8, and ketorolac tromethamine instillation reduced IL-8 and PGE2, in aqueous humor of patients undergoing femtosecond laser surgery, with the combination of both eyedrops being more effective than either alone. Fluorometholone 25-40 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 34625847-11 2022 CONCLUSION: Preoperative fluorometholone instillation reduced IL-8, and ketorolac tromethamine instillation reduced IL-8 and PGE2, in aqueous humor of patients undergoing femtosecond laser surgery, with the combination of both eyedrops being more effective than either alone. Ketorolac Tromethamine 72-94 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 34626114-6 2022 The results of q-PCR analysis showed that metformin reduced NF-kappaB mediated inflammatory response including decreased level of pro-inflammatory cytokine IL-8 and increased expression of anti-inflammatory cytokine IL-10 in gut of the fish with natural aging and poly I:C-injected 6-month-old fish. Metformin 42-51 C-X-C motif chemokine ligand 8 Homo sapiens 156-160 34690806-4 2021 Our results showed that the reactive oxygen species (ROS)/STIM1/Ca2+ axis played a critical role in CS-induced secretion of interleukin (IL)-8 in human alveolar macrophages. Reactive Oxygen Species 53-56 C-X-C motif chemokine ligand 8 Homo sapiens 124-142 34690806-11 2021 Furthermore, pretreatment with SKF-96365 and 2-APB, the inhibitors of Ca2+ influx, suppressed CSE-induced secretion of IL-8. 1-(2-(3-(4-methoxyphenyl)propoxy)-4-methoxyphenylethyl)-1H-imidazole 31-40 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 34690806-11 2021 Furthermore, pretreatment with SKF-96365 and 2-APB, the inhibitors of Ca2+ influx, suppressed CSE-induced secretion of IL-8. 2-aminoethoxydiphenyl borate 45-50 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 34690806-12 2021 In conclusion, our study demonstrates that CSE-induced ROS production may increase the expression of STIM1 in macrophages, which further promotes the release of IL-8 by regulating Ca2+ entry. Reactive Oxygen Species 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 161-165 34303665-1 2021 The aim of the current study was to perform a meta-analysis of randomized clinical trials regarding the effect of resveratrol in decreasing the levels of inflammatory cytokines, including interleukin (IL)-1, IL-6, IL-8, and tumor necrosis factor (TNF)-alpha in a combination of inflammatory diseases. Resveratrol 114-125 C-X-C motif chemokine ligand 8 Homo sapiens 214-218 34690948-12 2021 Serum IL-8 levels were significantly lower after FMT than at baseline, but IL-4, IL-6, IL-10, and IL-12p70 levels were not noticeably changed. fmt 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 6-10 34638448-5 2021 Increasing levels of IL6, IL8, CXCL16, MPIF1, and YKL40 correlated with increasing levels of ceramide in both cohorts. Ceramides 93-101 C-X-C motif chemokine ligand 8 Homo sapiens 26-29 34289703-1 2021 OBJECTIVE: 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) imaging is thought to visualize active atherosclerotic plaque calcification. 18f-sodium fluoride 11-30 C-X-C motif chemokine ligand 8 Homo sapiens 36-39 34671275-13 2021 CXCL8, IL6, and IL1B were increased by the MRTF-SRF inhibitor CCG-1423 and by MRTF-A silencing in hCASMCs, but depolymerization of actin, known to inhibit MRTF activity, had no stimulatory effect, an exception being IL1B. CCG 1423 62-70 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 34115201-10 2021 RESULTS: The dentifrices placebo and NaF in the low flow presented lower SMH and higher Ra in T3 and lower Ca% compared to the same dentifrices in normal flow. Radium 88-90 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 34688464-5 2021 The results suggested that Neo decreased the levels of interleukin IL-1beta, IL-6, IL-8, TNF-alpha, MMP-3, MMP-9 and MMP-13 in FLSs. neohesperidin 27-30 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 34115201-10 2021 RESULTS: The dentifrices placebo and NaF in the low flow presented lower SMH and higher Ra in T3 and lower Ca% compared to the same dentifrices in normal flow. Triiodothyronine 94-96 C-X-C motif chemokine ligand 8 Homo sapiens 37-40 34308732-7 2021 Quercetin decreased the production of IL-1beta, IL-6, IL-8, TNF-alpha, iNOS, and COX-2, as well as signal transduction via the Akt/AMPK/mTOR pathway. Quercetin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 34555226-3 2021 Prior studies indicated that IL-8-induced heterologous desensitization of the beta2-adrenergic receptor (beta2 -AR) led to decreased beta-agonist-induced mobilization of cyclic adenosine monophosphate (cAMP). Adenosine 177-186 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 34555226-3 2021 Prior studies indicated that IL-8-induced heterologous desensitization of the beta2-adrenergic receptor (beta2 -AR) led to decreased beta-agonist-induced mobilization of cyclic adenosine monophosphate (cAMP). Cyclic AMP 202-206 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 34189835-3 2021 Exposure to Pb nanoparticles for 24 h at a concentration of 100 mug/ml induced interleukin-8 (IL-8) expression in dTHP-1 cells. Lead 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 79-92 34189835-3 2021 Exposure to Pb nanoparticles for 24 h at a concentration of 100 mug/ml induced interleukin-8 (IL-8) expression in dTHP-1 cells. Lead 12-14 C-X-C motif chemokine ligand 8 Homo sapiens 94-98 34615379-7 2021 PRO reduced the cytokine levels of TNF-alpha, IL-12 and IL-8 and inhibited tyrosinase. Proline 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 34403670-5 2021 More interestingly, the higher MW digesta fraction containing the partially degraded EPS-LM showed even stronger inhibiting activity than the original EPS-LM on the LPS-induced pro-inflammatory responses in THP-1 cell culture, including NF-kappaB activation, release of NO, TNF-alpha and IL-8. eps 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 288-292 34431007-4 2021 It was found that different concentrations of melatonin could significantly inhibit the expression levels of NFkappaB and its downstream cytokines, including IL6 and IL8 in Caco-2 cells (*P < 0.05, **P < 0.01), 3D intestinal organoids (*P < 0.05, **P < 0.01) and intestinal explants (*P < 0.05, **P < 0.01). Melatonin 46-55 C-X-C motif chemokine ligand 8 Homo sapiens 166-169 34431007-5 2021 Melatonin abolished the activation of LPS on the expression levels of NFkappaB, IL6, and IL8 in three intestinal models (*P < 0.05, **P < 0.01, ***P < 0.001). Melatonin 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 89-92 34143519-9 2021 We also found significant changes in the cytokine profile after radioiodine ablation, including the decrease of tumor necrosis factor-alpha and IL-8 (P < 0.001, P < 0.001, respectively), and increase of IL-2R (P < 0.001). Iodine-131 64-75 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34398388-4 2021 BBB integrity and function were assessed via transendothelial electrical resistance (TEER) and paracellular flux of sodium fluorescein (NaF, 376 Da). Fluorescein 116-134 C-X-C motif chemokine ligand 8 Homo sapiens 136-139 34514543-10 2021 Conversely, alpha7 nAChR-specific agonist GTS-21 diminished the release of interleukin-1beta (IL-1beta), IL-6, IL-8, and tumor necrosis factor-alpha (TNFalpha) in SH-SY5Y cells under inflammatory conditions. 3-(2,4-dimethoxybenzylidene)anabaseine 42-48 C-X-C motif chemokine ligand 8 Homo sapiens 111-115 34601834-11 2021 CONCLUSION: Sodium fluoride (NaF) should be used as preservative to avoid ethanol neo-genesis during storage and transportation of blood samples for alcohol analysis. Sodium Fluoride 12-27 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 34601834-11 2021 CONCLUSION: Sodium fluoride (NaF) should be used as preservative to avoid ethanol neo-genesis during storage and transportation of blood samples for alcohol analysis. Ethanol 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 29-32 34127514-6 2021 Compared with the non-IPA group, the proven/probable IPA group showed significantly elevated levels of IL-6 and IL-8 in both serum and BALF, which were positively correlated with galactomannan levels. galactomannan 179-192 C-X-C motif chemokine ligand 8 Homo sapiens 112-116 34638857-8 2021 Furthermore, IL-8/MCP-1 mRNA/protein was amplified in monocytic cells following stimulation with TNF-alpha in the presence of H2O2 or hypoxia (p 0.0001). Hydrogen Peroxide 126-130 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 34333067-3 2021 A 24 hour exposure increased IL-8 release at an SDS concentration >=0.63 mM (0.018%, w/v). Sodium Dodecyl Sulfate 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 29-33 34151709-6 2021 We showed that sodium fluoride (NaF) reduces cell viability in a concentration-dependent manner (p < 0.05) up to a 96-h time-point when compared to control. Sodium Fluoride 15-30 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 34216363-11 2021 Secondly, the excessive production of inflammatory factors (IL-1beta, IL-8, and MCP-1) and adhesion molecules (ICAM-1 and VCAM-1) triggered by propofol was pronouncedly inhibited by Benzbromarone. Propofol 143-151 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 34216363-11 2021 Secondly, the excessive production of inflammatory factors (IL-1beta, IL-8, and MCP-1) and adhesion molecules (ICAM-1 and VCAM-1) triggered by propofol was pronouncedly inhibited by Benzbromarone. Benzbromarone 182-195 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 34603464-0 2021 Polyphyllin I Inhibits Propionibacterium acnes-Induced IL-8 Secretion in HaCaT Cells by Downregulating the CD36/NOX1/ROS/NLRP3/IL-1beta Pathway. polyphyllin I 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 34468398-9 2021 TSH levels were inversely correlated with IL-8 (r = -0.248), IL-10 (r = -0.253), IL-15 (r = -0.213), IP-10 (r = -0.334) and GM-CSF (r = -0.254). Thyrotropin 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 34584119-8 2021 Moreover, metformin also triggered mRNA expression of the proinflammatory cytokines IL1B, CXCL8 and growth factor GDF15 in human uroepithelial cells. Metformin 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 90-95 34231590-7 2021 Our work confirms that Na3FeF6 undergoes conversion into NaF and Fe(s) nanoparticles. na3fef6 23-30 C-X-C motif chemokine ligand 8 Homo sapiens 57-60 34611474-8 2021 Treatment with Imipridones decreased CCL3/MIP-1 alpha, VEGF, CXCL14/BRAK, IL-8/CXCL8, and Prolactin and increased CXCL5/ENA-78. imipridones 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 34611474-8 2021 Treatment with Imipridones decreased CCL3/MIP-1 alpha, VEGF, CXCL14/BRAK, IL-8/CXCL8, and Prolactin and increased CXCL5/ENA-78. imipridones 15-26 C-X-C motif chemokine ligand 8 Homo sapiens 79-84 34611476-9 2021 There was an increase in IL-8 by oxaliplatin and increase in ferritin by cisplatin which may contribute to cancer cell survival. Oxaliplatin 33-44 C-X-C motif chemokine ligand 8 Homo sapiens 25-29 34603464-4 2021 Reactive oxygen species (ROS) acts as a trigger for the production of IL-8 and activates theNLRP3 inflammasome. Reactive Oxygen Species 0-23 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 34603464-4 2021 Reactive oxygen species (ROS) acts as a trigger for the production of IL-8 and activates theNLRP3 inflammasome. Reactive Oxygen Species 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 34355225-7 2021 The interleukin (IL)-1beta-induced release of inflammatory cytokines IL-8 and tumor necrosis factor (TNF)-alpha in human chondrosarcoma cells was inhibited by monapurpureusone (8) and monascuspirolide B (14). Monascuspirolide B 184-202 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 34355225-7 2021 The interleukin (IL)-1beta-induced release of inflammatory cytokines IL-8 and tumor necrosis factor (TNF)-alpha in human chondrosarcoma cells was inhibited by monapurpureusone (8) and monascuspirolide B (14). monapurpureusone 159-175 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 34536415-8 2022 RESULTS: Mutant HCK lacking the C-terminal inhibitory tyrosine Tyr522 exhibited increased kinase activity and enhanced myeloid cell priming, migration and effector functions, such as production of the inflammatory cytokines IL-1beta, IL-6, IL-8 and TNFalpha and production of reactive oxygen species. Tyrosine 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 240-244 34632188-7 2021 Furthermore, 1,4-naphthoquinone potently suppressed the production and secretion of key proinflammatory cytokine proteins IL-8, IL-1beta, IL-10, TNF-alpha, and IL-6 in LPS-stimulated PMA-induced human THP-1 macrophages. 1,4-naphthoquinone 13-31 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 34579097-7 2021 For metabolic and inflammatory factors, the participants in the CR-RS group showed significant decreases in low density lipoprotein cholesterol (-0.40 mmol/L) and interleukin-8 (-0.73 mmol/L). cr-rs 64-69 C-X-C motif chemokine ligand 8 Homo sapiens 163-176 34519008-1 2021 BACKGROUND: While (18F)-fluordeoxyglucose ((18F)FDG) uptake is associated with arterial inflammation, (18F)-sodium fluoride ((18F)NaF) is a marker for arterial micro-calcification. (18f)-sodium fluoride 102-123 C-X-C motif chemokine ligand 8 Homo sapiens 130-133 34524489-4 2022 18F-sodium fluoride (NaF) PET/CT is an excellent bone-seeking agent superior to conventional bone scan in CKD patients due to its high bone uptake, rapid single-pass extraction, and minimal binding to serum proteins. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 21-24 34493652-3 2021 We demonstrate that selective zwitterion-anion interactions simultaneously control salt partitioning and diffusivity, with the permeabilities of NaClO4, NaI, NaBr, NaCl, NaF, and Na2SO4 spanning roughly three orders of magnitude over a wide range of feed concentrations. Anions 41-46 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 34493652-3 2021 We demonstrate that selective zwitterion-anion interactions simultaneously control salt partitioning and diffusivity, with the permeabilities of NaClO4, NaI, NaBr, NaCl, NaF, and Na2SO4 spanning roughly three orders of magnitude over a wide range of feed concentrations. Salts 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 170-173 34493195-7 2022 RESULTS: We filtered out 6 pivotal ingredients from QFPDD by using the bioinformatics method, namely quercetin, luteolin, berberine, hederagenin, shionone and kaempferol, which can inhibit the highly expressed genes (i.e. CXCR4, ICAM1, CXCL8, CXCL10, IL6, IL2, CCL2, IL1B, IL4, IFNG) in severe COVID-19 patients. Quercetin 101-110 C-X-C motif chemokine ligand 8 Homo sapiens 236-241 34495872-7 2021 Administration of IPI504 at 0.5-5 muM can significantly inhibit the induction of IL-1beta, IL-6, IL-8, MCP-1 and VEGFA in senescent ARPE-19 and the senescence-mediated migration of retinal capillary endothelial cells in vitro. tanespimycin 18-24 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 34568366-5 2021 Results: IL-6, IL-8, IP-10, and MCP-1 in aqueous humor of DME vitrectomized eyes were significantly higher than in non-vitrectomized DME eyes, while VEGF was lower than in non-vitrectomized DME eyes. dme 58-61 C-X-C motif chemokine ligand 8 Homo sapiens 15-19 34493195-7 2022 RESULTS: We filtered out 6 pivotal ingredients from QFPDD by using the bioinformatics method, namely quercetin, luteolin, berberine, hederagenin, shionone and kaempferol, which can inhibit the highly expressed genes (i.e. CXCR4, ICAM1, CXCL8, CXCL10, IL6, IL2, CCL2, IL1B, IL4, IFNG) in severe COVID-19 patients. hederagenin 133-144 C-X-C motif chemokine ligand 8 Homo sapiens 236-241 34493195-7 2022 RESULTS: We filtered out 6 pivotal ingredients from QFPDD by using the bioinformatics method, namely quercetin, luteolin, berberine, hederagenin, shionone and kaempferol, which can inhibit the highly expressed genes (i.e. CXCR4, ICAM1, CXCL8, CXCL10, IL6, IL2, CCL2, IL1B, IL4, IFNG) in severe COVID-19 patients. shionone 146-154 C-X-C motif chemokine ligand 8 Homo sapiens 236-241 34493195-7 2022 RESULTS: We filtered out 6 pivotal ingredients from QFPDD by using the bioinformatics method, namely quercetin, luteolin, berberine, hederagenin, shionone and kaempferol, which can inhibit the highly expressed genes (i.e. CXCR4, ICAM1, CXCL8, CXCL10, IL6, IL2, CCL2, IL1B, IL4, IFNG) in severe COVID-19 patients. kaempferol 159-169 C-X-C motif chemokine ligand 8 Homo sapiens 236-241 34572676-5 2021 The biomedical field has the highest need of AMPs as it possesses prominent desirable activity against HIV-1, skin cancer, breast cancer, in Behcet"s disease treatment, as well as in reducing the release of inflammatory cells such as TNFalpha, IL-8, and IL-1beta, enhancing the production of anti-inflammatory cytokines such as IL-10 and GM-CSF, and in wound healing properties. Adenylyl sulfate 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 244-248 34566947-12 2021 Protease allergen of nTyr-p3 significantly increased the levels of pro-inflammatory cytokines (IL-6 and TNF-alpha), chemokine (IL-8), and IL-1beta in epithelial cells. ntyr-p3 21-28 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 34566947-17 2021 Among the pharmacologic inhibitors, the most effective inhibitor of the nTyr-p3 in the induction of IL-8 or IL-1beta levels was GB88 followed by SBTI, MAPK/ERK, ERK, and p38 inhibitors. ntyr-p3 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 34566947-17 2021 Among the pharmacologic inhibitors, the most effective inhibitor of the nTyr-p3 in the induction of IL-8 or IL-1beta levels was GB88 followed by SBTI, MAPK/ERK, ERK, and p38 inhibitors. GB88 128-132 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 34493195-7 2022 RESULTS: We filtered out 6 pivotal ingredients from QFPDD by using the bioinformatics method, namely quercetin, luteolin, berberine, hederagenin, shionone and kaempferol, which can inhibit the highly expressed genes (i.e. CXCR4, ICAM1, CXCL8, CXCL10, IL6, IL2, CCL2, IL1B, IL4, IFNG) in severe COVID-19 patients. Luteolin 112-120 C-X-C motif chemokine ligand 8 Homo sapiens 236-241 34493195-7 2022 RESULTS: We filtered out 6 pivotal ingredients from QFPDD by using the bioinformatics method, namely quercetin, luteolin, berberine, hederagenin, shionone and kaempferol, which can inhibit the highly expressed genes (i.e. CXCR4, ICAM1, CXCL8, CXCL10, IL6, IL2, CCL2, IL1B, IL4, IFNG) in severe COVID-19 patients. Berberine 122-131 C-X-C motif chemokine ligand 8 Homo sapiens 236-241 34572313-12 2021 In conclusion, we discovered that cross-talk between FcgammaRIII engagement-induced Syk-ERK and PMA-induced PKC signaling pathways augment NET formation of dHL-60 via increased ROS generation and pro-inflammatory cytokines, IL-8 and TNF-alpha, production. Tetradecanoylphorbol Acetate 96-99 C-X-C motif chemokine ligand 8 Homo sapiens 224-228 34557089-0 2021 Platinum Accumulation and Cancer-Related Fatigue, Correlation With IL-8, TNF-alpha and Hemocytes. Platinum 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 34557089-7 2021 Mediating effect analysis showed that increased IL-8 concentration mediated 57.4%, while decreased erythrocyte count mediated 24.1% of the C-Pt effect on CRF. c-pt 139-143 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 34557089-8 2021 Platinum accumulation may involve increasing IL-8, cause inflammation or aggravate anemia, which in combination lead to CRF. Platinum 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 45-49 34573967-6 2021 The serum IL-8 and TNF-alpha concentration measured in the OC Group was significantly higher than in the BOC Group (p < 0.05). boc 105-108 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 34482382-3 2021 By analyzing transcriptome of enzalutamide-resistant prostate cancer cells, we found that resistance was conferred by a mild caspase-8 upregulation that in turn led to NF-kappaB activation and the subsequent upregulation of the downstream IL-8. enzalutamide 30-42 C-X-C motif chemokine ligand 8 Homo sapiens 239-243 34482382-7 2021 Collectively, our work demonstrates that enzalutamide-resistance is mediated by caspase-8 upregulation and the consequent increase in NF-kappaB/IL-8 mediated survival signaling, highlighting caspase-8 and NF-kappaB as potential therapeutic targets to overcome enzalutamide-resistance in CRPC. enzalutamide 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34080770-7 2021 Meanwhile, we demonstrated that miR-486-3p regulates NaF-induced upregulation of CyclinD1 by directly targeting its 3"-untranslated region (3"-UTR). p-Bis(2-chloroethyl)amino-o-methoxyphenylalanine 40-42 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 34280354-5 2021 In addition, the expression of various genes involved in carcinogenesis, namely, NFE2L2 (antioxidative response), CXCL8 (inflammation), CDH1 (cell adhesion), MMP9 (tissue remodeling) and MKI67 (cell proliferation) were altered in cholangiocytes treated with DCM. Methylene Chloride 258-261 C-X-C motif chemokine ligand 8 Homo sapiens 114-119 34280354-7 2021 In malignant cell lines (HuCCA-1 and RMCCA-1), DCM treatment resulted in increased CXCL8 and MMP9 transcription and decreased CDH1 transcription accompanied by increased invasion and migration capabilities of these cells. Methylene Chloride 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 83-88 34080770-6 2021 Further, we verified that sodium fluoride (NaF) decreases miR-486-3p expression in human osteoblasts and overexpression of miR-486-3p reduces fluoride-induced osteoblast proliferation and activation. Sodium Fluoride 26-41 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 34412775-9 2021 The fluorine mainly as the formation of substantial NaF and CaF2 in the residual ash. Fluorine 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 52-55 34080770-6 2021 Further, we verified that sodium fluoride (NaF) decreases miR-486-3p expression in human osteoblasts and overexpression of miR-486-3p reduces fluoride-induced osteoblast proliferation and activation. Fluorides 142-150 C-X-C motif chemokine ligand 8 Homo sapiens 43-46 34080770-7 2021 Meanwhile, we demonstrated that miR-486-3p regulates NaF-induced upregulation of CyclinD1 by directly targeting its 3"-untranslated region (3"-UTR). mir-486 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 53-56 34610759-3 2021 Results: MiR-101-3p was increased in the NS patients and the dysregulation of miR-101-3p was associated with levels of procalcitonin, CRP, IL-8 and TNF-alpha. mir-101-3p 78-88 C-X-C motif chemokine ligand 8 Homo sapiens 139-143 34610759-5 2021 The silenced miR-101-3p reversed the increased levels of TNF-alpha and IL-8 caused by lipopolysaccharide in vitro. mir-101-3p 13-23 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 34502382-10 2021 These results suggest that PAI-1 and IL-8 produced by OSCC contribute to the differentiation of monocytes to CD206+ TAMs. tams 116-120 C-X-C motif chemokine ligand 8 Homo sapiens 37-41 34497153-9 2021 IPA analysis revealed ibuprofen having modulating effects on inflammation-related pathways such as integrin, IL-8, ERK/MAPK and cAMP-mediated signalling pathways. Ibuprofen 22-31 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 34252445-3 2021 Based on our experimental data, 24 hours after treatment with fusarotoxins, hydrogen peroxide levels, intracellular oxidative stress and the amounts of inflammatory interleukins IL-6 and IL-8 significantly increased. fusarotoxins 62-74 C-X-C motif chemokine ligand 8 Homo sapiens 187-191 34512648-8 2021 In preterm infants, exposure to HCA was associated with elevations in 8 immune proteins on postnatal day 5 (BDNF, C3, C5a, C9, IL-8, MCP-1, MIP-1beta and MMP-9) when compared to preterm infants who were not exposed. hca 32-35 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 34415898-9 2021 Overall, IL-4 levels did not change significantly over time in either group; however, patients within the CE3b group showed a significant decrease of IL-1ra, IL-6, IL-8, G-CSF, IFN-gamma, IP-10, MCP-1, MIP-1alpha, FGF at T1 compared to T0 (p<=0.042). ce3b 106-110 C-X-C motif chemokine ligand 8 Homo sapiens 164-168 34513587-7 2021 In this article we intend to present different patterns of OA (mild to severe stages of OA) that we had observed on 18F-Sodium Fluoride (18F-NaF) PET/MRI. 18f-sodium fluoride 116-135 C-X-C motif chemokine ligand 8 Homo sapiens 141-144 34426617-4 2021 The DMEK group exhibited significantly lower concentrations of several pro-inflammatory cytokines, such as IL-1beta, IL-5, IL-6, IL-10, and IL-8, and granulocyte colony stimulating factor than the BK group. dmek 4-8 C-X-C motif chemokine ligand 8 Homo sapiens 140-144 34504537-8 2021 EFE inhibited the expression of MMP-1, MMP-3, and proinflammatory cytokines (TNF-alpha, IL-6, and IL-8) in IL-1beta-stimulated HGFs through the inhibition of IL-1beta-induced MAPK/STAT-3 activation. EFE 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 98-102 34412678-10 2021 In addition, we discovered that ASFV infection is involved in the regulation of chemokine expression in PAMs, and the chemokines, such as C-X-C motif chemokine 8 (CXCL8) and CXCL10, were upregulated after infection. c-x-c 138-143 C-X-C motif chemokine ligand 8 Homo sapiens 163-168 34497913-3 2021 The significant amplifying actions of two PAHs, dibenzo(a,l)pyrene (DB(a,l)P) at 50 nM and dibenzo(a,i)pyrene (DB(a,i)P) at 2 muM for 48 h, for IL-8 protein release induced by mite antigens in epithelial cells were observed for the first time. dibenzo(a,l)pyrene 48-66 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34497913-3 2021 The significant amplifying actions of two PAHs, dibenzo(a,l)pyrene (DB(a,l)P) at 50 nM and dibenzo(a,i)pyrene (DB(a,i)P) at 2 muM for 48 h, for IL-8 protein release induced by mite antigens in epithelial cells were observed for the first time. dibenzo(a,l)pyrene 68-76 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34497913-3 2021 The significant amplifying actions of two PAHs, dibenzo(a,l)pyrene (DB(a,l)P) at 50 nM and dibenzo(a,i)pyrene (DB(a,i)P) at 2 muM for 48 h, for IL-8 protein release induced by mite antigens in epithelial cells were observed for the first time. dibenzo(a,i)pyrene 91-109 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34497913-3 2021 The significant amplifying actions of two PAHs, dibenzo(a,l)pyrene (DB(a,l)P) at 50 nM and dibenzo(a,i)pyrene (DB(a,i)P) at 2 muM for 48 h, for IL-8 protein release induced by mite antigens in epithelial cells were observed for the first time. dibenzo(a,i)pyrene 111-119 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34445582-6 2021 An experiment with an antibody array for 25 angiogenesis-related proteins revealed that only interleukin-8 expression was significantly upregulated in HUVECs treated with ADSC-LPS-exo. adsc-lps 171-179 C-X-C motif chemokine ligand 8 Homo sapiens 93-106 34445558-11 2021 The conditioned medium obtained from IronQ-treated PBMCs contained high levels of interleukin 8 (IL-8), IL-10, urokinase-type-plasminogen-activator (uPA), matrix metalloproteinases-9 (MMP-9), and tumor necrosis factor-alpha (TNF-alpha), as well as augmented migration and capillary network formation of HUVECs and fibroblast cells, in vitro. ironq 37-42 C-X-C motif chemokine ligand 8 Homo sapiens 82-95 34445558-11 2021 The conditioned medium obtained from IronQ-treated PBMCs contained high levels of interleukin 8 (IL-8), IL-10, urokinase-type-plasminogen-activator (uPA), matrix metalloproteinases-9 (MMP-9), and tumor necrosis factor-alpha (TNF-alpha), as well as augmented migration and capillary network formation of HUVECs and fibroblast cells, in vitro. ironq 37-42 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 34445390-6 2021 LPS-induced activation of NFAT-regulated cytokines (IL-6 and IL-8) is inhibited by treatment of cells with VIVIT. NFAT Inhibitor 107-112 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 34429629-11 2021 In DNPCs, ATP and IL-1alpha induced the expression of IL-8 and CXCL-1. Adenosine Triphosphate 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 34441355-2 2021 With regard to tracer, there has been a shift from using mainly 18F-fluorodeoxyglucose (FDG), indicating inflammation, to applying predominantly 18F-sodium fluoride (NaF) due to its high affinity for arterial wall microcalcification and more consistent association with cardiovascular risk factors. 18f-sodium fluoride 145-164 C-X-C motif chemokine ligand 8 Homo sapiens 166-169 34452455-7 2021 When the models were challenged with a combination of the bacterial toxins LPS and ATP, a release of the proinflammatory cytokines IL-1beta and IL-8 was observed, confirming that the model can generate an immune response. Adenosine Triphosphate 83-86 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34286584-0 2021 Nanoparticles for Directed Immunomodulation: Mannose-Functionalized Glycodendrimers Induce Interleukin-8 in Myeloid Cell Lines. Mannose 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 91-104 34286584-3 2021 This design enhanced glycodendrimer bioactivity and led to complex functional effects in myeloid cells, with specific induction of interleukin-8 expression by mannose glycodendrimers detected in HL-60 and THP-1 cells. mannose glycodendrimers 159-182 C-X-C motif chemokine ligand 8 Homo sapiens 131-144 34363384-8 2021 Knockdown of IL-8 abolished Lefty-regulated sunitinib sensitivity of RCC cells. Sunitinib 44-53 C-X-C motif chemokine ligand 8 Homo sapiens 13-17 34318676-0 2021 Experimental and Computational Exploration of the NaF-ThF4 Fuel System: Structure and Thermochemistry. thf4 54-58 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 34443321-3 2021 The effect of BBR on AA/LPS activated proinflammatory markers including TNF-alpha, MCP-1, IL-8 and COX-2 was measured by ELISA or quantitative real-time PCR. Berberine 14-17 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 34318676-3 2021 The phase equilibria in the 10-50 mol % ThF4 and 85-95 mol % ThF4 regions of the NaF-ThF4 phase diagram were measured using differential scanning calorimetry, as were the mixing enthalpies at 1266 K of (NaF/ThF4) = (0.8:0.2), (0.7:0.3) mixtures. thf4 61-65 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 34318676-3 2021 The phase equilibria in the 10-50 mol % ThF4 and 85-95 mol % ThF4 regions of the NaF-ThF4 phase diagram were measured using differential scanning calorimetry, as were the mixing enthalpies at 1266 K of (NaF/ThF4) = (0.8:0.2), (0.7:0.3) mixtures. thf4 85-89 C-X-C motif chemokine ligand 8 Homo sapiens 81-84 34443321-5 2021 AA/ LPS-induced TNF-alpha, MCP-1, IL-6, IL-8, and COX-2 markers were markedly attenuated by BBR treatment in THP-1 cells by inhibiting NF-kappaB translocation into the nucleus. Berberine 92-95 C-X-C motif chemokine ligand 8 Homo sapiens 40-44 34229236-8 2021 Present article highlights new mechanistic insights through which DMB inhibits ROS/RNS, oxidative stress, mitochondrial dysfunctions and neuroinflammation such as NFkappaB, TNF-alpha, IL-6 and IL-8, cytokinin. demethyleneberberine 66-69 C-X-C motif chemokine ligand 8 Homo sapiens 193-197 34348775-1 2021 BACKGROUND: Silver diamine fluoride (SDF) and sodium fluoride (NaF) are widely used for caries management. Sodium Fluoride 46-61 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 34424286-6 2021 Results: In the MDR-PA group, significantly (P < 0.05) increased expression of IL-6, IL-8, IL-10, IL-1beta, and TNF-alpha was observed in comparison with the S-PA group. mdr-pa 16-22 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 34424286-6 2021 Results: In the MDR-PA group, significantly (P < 0.05) increased expression of IL-6, IL-8, IL-10, IL-1beta, and TNF-alpha was observed in comparison with the S-PA group. s-pa 158-162 C-X-C motif chemokine ligand 8 Homo sapiens 85-89 34372688-10 2021 IL-1beta-induced inflammation, assessed by IL-1beta, IL-8, and tumour necrosis factor alpha (TNF-alpha) upregulation, was alleviated by suramin treatment. Suramin 136-143 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 34459125-8 2021 Subsequently, TNF-alpha, IL-1beta, and lactate activated CAFs, and facilitated the secretion of IL-6, IL-7, IL-8, CCL5, and transforming growth factor-beta1 from CAFs. Lactic Acid 39-46 C-X-C motif chemokine ligand 8 Homo sapiens 108-112 34241784-4 2021 Characellide A induces a concentration- and time-dependent CXCL8, IL-6 and TNF-alpha release from PBMC. characellide a 0-14 C-X-C motif chemokine ligand 8 Homo sapiens 59-64 34097917-6 2021 RESULTS: IL-8 urinary levels were increased in patients with T2D and diabetic kidney disease, with the highest urinary IL-8 levels found in the patients with the largest decline in glomerular filtration rate, with an increased albumin/creatine ratio and the worst renal outcome. Creatine 235-243 C-X-C motif chemokine ligand 8 Homo sapiens 9-13 34097917-8 2021 High glucose elicits abundant IL-8 secretion in cultured human immortalized podocytes in vitro. Glucose 5-12 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 34439789-6 2021 Significant correlations were found with PHE volume for IL-6, IL-10 and CCL2 at day 1-2 and with relative PHE at days 7-8 or 9-10 for IL-1beta, IL-6, IL-8, and IL-10. Phenylalanine 106-109 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 34355287-8 2021 Moreover, BDMC-A treatment downregulated MMP-9, VEGF, TGF- beta, IL-6 and IL-8 and upregulated TIMP-2 levels. bdmc-a 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 34296555-8 2021 The concentrations of Cr, Ni, and Au ions in the saliva were positively correlated with IL-8. Chromium 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 34296555-8 2021 The concentrations of Cr, Ni, and Au ions in the saliva were positively correlated with IL-8. Gold 34-36 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 34296555-10 2021 CONCLUSION: Increased concentrations of metal ions, especially Ni, in saliva were positively correlated with IL-8 and showed positive correlations with the severity of OLL. Metals 40-45 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 34361481-5 2021 MAO coatings were successfully prepared on the surface of Zn-Mn-Mg alloys by MAO in silicate-based solutions with different NaF concentrations. 5'-DEOXY-5'-[N-METHYL-N-(2-AMINOOXYETHYL) AMINO]ADENOSINE 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 34361481-5 2021 MAO coatings were successfully prepared on the surface of Zn-Mn-Mg alloys by MAO in silicate-based solutions with different NaF concentrations. zn-mn 58-63 C-X-C motif chemokine ligand 8 Homo sapiens 124-127 34361481-6 2021 The microstructure and phase composition of MAO coatings prepared on Zn-Mn-Mg alloys with different NaF concentrations in the electrolyte was examined by a scanning electron microscope and X-ray diffraction. 5'-DEOXY-5'-[N-METHYL-N-(2-AMINOOXYETHYL) AMINO]ADENOSINE 44-47 C-X-C motif chemokine ligand 8 Homo sapiens 100-103 34361481-11 2021 The highest corrosion rate can be achieved after MAO treatment, with an electrolyte concentration of 1.5 g/L NaF in Hank"s solution. 5'-DEOXY-5'-[N-METHYL-N-(2-AMINOOXYETHYL) AMINO]ADENOSINE 49-52 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 34110092-7 2021 Our findings suggest that p-gliadin composed of supramolecular structures triggers significant mRNA up-regulation (p < 0.05) of pro-apoptotic biomarkers (ratio Bcl2/Bak-1), chemokines (CCL2, CCL3, CCL4, CCL5, CXCL8) and the chemokine receptor CXCR3. p-gliadin 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 209-214 34250537-0 2021 Stabilizing Na metal anode with NaF interface on spent cathode carbon from aluminum electrolysis. Carbon 63-69 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 34361481-11 2021 The highest corrosion rate can be achieved after MAO treatment, with an electrolyte concentration of 1.5 g/L NaF in Hank"s solution. hank"s solution 116-131 C-X-C motif chemokine ligand 8 Homo sapiens 109-112 34250537-0 2021 Stabilizing Na metal anode with NaF interface on spent cathode carbon from aluminum electrolysis. Aluminum 75-83 C-X-C motif chemokine ligand 8 Homo sapiens 32-35 34250537-1 2021 We report the synthesis of spent cathode carbon (SCC) with a NaF interface from aluminum electrolysis, and its application as a Na metal anode host. Carbon 41-47 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 34250537-1 2021 We report the synthesis of spent cathode carbon (SCC) with a NaF interface from aluminum electrolysis, and its application as a Na metal anode host. Aluminum 80-88 C-X-C motif chemokine ligand 8 Homo sapiens 61-64 34368356-10 2021 NaF is effective in enhancing the enamel/dentin bond durability and also helps create a high quality of ARBZ to improve the clinical success of restorations. arbz 104-108 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 34438645-6 2021 Proteomics analysis of cytokines showed that niacin supplementation increased the expression of duodenal transforming growth factor-beta (TGF-beta), jejunal interleukin-10 (IL-10) and ileal interleukin-6 (IL-6) (p < 0.05), and reduced the expression of ileal interleukin-8 (IL-8) (p < 0.05) compared with the control diet. Niacin 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 253-272 34438645-6 2021 Proteomics analysis of cytokines showed that niacin supplementation increased the expression of duodenal transforming growth factor-beta (TGF-beta), jejunal interleukin-10 (IL-10) and ileal interleukin-6 (IL-6) (p < 0.05), and reduced the expression of ileal interleukin-8 (IL-8) (p < 0.05) compared with the control diet. Niacin 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 274-278 34439757-6 2021 Additionally, the RA-RF significantly reduced ROS production, IL-6, IL-8, TNF-alpha, and COX-2. rosmarinic acid 18-20 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 34369925-6 2021 Similar percent drops in metabolic activity of the iHCEC and pHCEC occurred after exposure to BAK, H2O2, or SDS, and the most significant changes in cytokine release occurred for IL-6 and IL-8. Hydrogen Peroxide 99-103 C-X-C motif chemokine ligand 8 Homo sapiens 188-192 34292876-7 2021 Agomelatine also suppressed the expression of TNF-alpha, IL-8, and IL-12, which are proinflammatory cytokines that promote endothelial dysfunction and atherogenesis. agomelatine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 34350063-4 2021 Alternol triggered ICD in prostate cancer cells, as evidenced by the release of damage-associated molecular patterns (DAMPs) (i.e., calreticulin, CALR; high mobility group protein B1, HMGB1; and adenosine triphosphate, ATP) and pro-inflammatory cytokine (i.e., interleukin (IL)-1alpha, IL-1beta, IL-6, and IL-8) expression. Alternol 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 306-310 34371919-6 2021 We showed that although TNF-alpha secretion was downregulated in both LPS-activated MPhi subtypes by caffeine, the secretion of IL-8, IL-6, and IL-1beta as well as the expression of Nod-like receptors was enhanced in M-MPhis, while it did not change in GM-MPhis. Caffeine 101-109 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 34280220-3 2021 TG6-44 significantly decreased A/X31-induced ROS and virus-induced inflammatory mediators in THP-1 cells (IL-6, IFN-gamma, MCP-1, TNF-alpha, MIP-1beta) and in human PBMC (IL-6, IL-8, TNF-alpha, MCP-1). 6-O-phosphono-D-tagatose 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 34299258-5 2021 Resveratrol inhibited degranulation and expression of cytokines and chemokines such as CXCL8, CCL2, CCL3, CCL4, and TNF-alpha in a dose-dependent manner. Resveratrol 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 87-92 34281061-3 2021 In monocytes/macrophages, vitamin D suppresses the production of the inflammatory cytokines TNF-alpha, IL-1beta, IL-6, and IL-8. Vitamin D 26-35 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 34299030-8 2021 TNFalpha stimulated the cytokine expression in FLS, and NDMVs down-regulated TNFalpha-induced expression of IL-5, IL-6, IL-8, MCP-1, IFNgamma and MIP-1beta. ndmvs 56-61 C-X-C motif chemokine ligand 8 Homo sapiens 120-124 34305638-16 2021 During alcohol detoxification, LS, transaminases, TGF- beta, IL-6, IL-8 and VEGF decreased significantly. Alcohols 7-14 C-X-C motif chemokine ligand 8 Homo sapiens 67-71 34262692-11 2021 Interleukin (IL)-8, IL-10, IL-1alpha, and tissue inhibitor of metalloproteinase (TIMP)-1 concentrations were significantly increased in the culture medium of cells exposed to PM2.5, and budesonide significantly reduced the changes in IL-8, IL-1alpha, and TIMP-1. Budesonide 186-196 C-X-C motif chemokine ligand 8 Homo sapiens 0-18 34262692-11 2021 Interleukin (IL)-8, IL-10, IL-1alpha, and tissue inhibitor of metalloproteinase (TIMP)-1 concentrations were significantly increased in the culture medium of cells exposed to PM2.5, and budesonide significantly reduced the changes in IL-8, IL-1alpha, and TIMP-1. Budesonide 186-196 C-X-C motif chemokine ligand 8 Homo sapiens 234-238 34114792-7 2021 Markedly, NCO-sP(EO-stat-PO)-rich samples induced a significantly reduced release of proinflammatory cytokines, IL-1beta, IL-6, and IL-8. nco-sp 10-16 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 34114792-7 2021 Markedly, NCO-sP(EO-stat-PO)-rich samples induced a significantly reduced release of proinflammatory cytokines, IL-1beta, IL-6, and IL-8. eo-stat-po 17-27 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 34152720-5 2021 Our results demonstrated that treatment with baicalein protects T98G cells from H2O2-induced damage, delays cell senescence, inhibits the secretion of SASP (IL-6, IL-8, TNF-alpha, CXCL1, and MMP-1), and inhibits SASP-related pathways NF-kappaB and JAK2/STAT1. baicalein 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 34227646-3 2021 It was observed that the expression of IL-1beta, IL-6, IL-8 and TNFalpha in LPS-induced HGFs was significantly downregulated by RSV in a dose-dependent manner. Resveratrol 128-131 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 34227646-6 2021 Subsequently, it was demonstrated treatment with PI3K/AKT pathway inhibitor (LY294002) or Wnt/beta-catenin pathway inhibitor (Dickkopf-1, DKK-1) could further enhance the anti-inflammatory and antioxidant effects of RSV by downregulating the expression of IL-1beta, IL-6, IL-8 and TNFalpha, and the production of MDA, and increasing the activity of SOD and GSH-Px in LPS-induced HGFs. 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one 77-85 C-X-C motif chemokine ligand 8 Homo sapiens 272-276 34227646-6 2021 Subsequently, it was demonstrated treatment with PI3K/AKT pathway inhibitor (LY294002) or Wnt/beta-catenin pathway inhibitor (Dickkopf-1, DKK-1) could further enhance the anti-inflammatory and antioxidant effects of RSV by downregulating the expression of IL-1beta, IL-6, IL-8 and TNFalpha, and the production of MDA, and increasing the activity of SOD and GSH-Px in LPS-induced HGFs. Resveratrol 216-219 C-X-C motif chemokine ligand 8 Homo sapiens 272-276 34414894-6 2021 Budesonide reduced synthesis of interleukin 4 (IL-4), CXCL8, tumor necrosis factor alpha (TNFalpha) by NK and NKT-like cells, as well as production of interferon gamma (IFNgamma) by NK cells. Budesonide 0-10 C-X-C motif chemokine ligand 8 Homo sapiens 54-59 34787252-2 2021 The specimens were exposed to mesoporous silica (MS) nanocomposites containing fluoride by association with titanium tetrafluoride (TiF4) or sodium fluoride (NaF). Sodium Fluoride 141-156 C-X-C motif chemokine ligand 8 Homo sapiens 158-161 34222847-10 2021 A decrease from baseline was higher in the NTZ group for d-Dimer (p = 0.001), US-RCP (p < 0.002), TNF (p < 0.038), IL-6 (p < 0.001), IL-8 (p = 0.014), HLA DR. on CD4+ T lymphocytes (p < 0.05), CD38 in CD4+ and CD8+ T (both p < 0.05), and CD38 and HLA-DR. on CD4+ (p < 0.01). nitazoxanide 43-46 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 34277625-4 2021 Here, we show that IL-8 secreted from CAFs could activate normal ovarian fibroblasts (NFs) through multiple signaling and that IL-8 stimulated malignant growth of ovarian cancer cells in animals and increased the IC50 of cisplatin (CDDP) in ovarian cancer cells. Cisplatin 221-230 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 34277625-4 2021 Here, we show that IL-8 secreted from CAFs could activate normal ovarian fibroblasts (NFs) through multiple signaling and that IL-8 stimulated malignant growth of ovarian cancer cells in animals and increased the IC50 of cisplatin (CDDP) in ovarian cancer cells. Cisplatin 221-230 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 34277625-4 2021 Here, we show that IL-8 secreted from CAFs could activate normal ovarian fibroblasts (NFs) through multiple signaling and that IL-8 stimulated malignant growth of ovarian cancer cells in animals and increased the IC50 of cisplatin (CDDP) in ovarian cancer cells. Cisplatin 232-236 C-X-C motif chemokine ligand 8 Homo sapiens 19-23 34277625-4 2021 Here, we show that IL-8 secreted from CAFs could activate normal ovarian fibroblasts (NFs) through multiple signaling and that IL-8 stimulated malignant growth of ovarian cancer cells in animals and increased the IC50 of cisplatin (CDDP) in ovarian cancer cells. Cisplatin 232-236 C-X-C motif chemokine ligand 8 Homo sapiens 127-131 34414894-8 2021 The combination of azithromycin and budesonide had a more pronounced inhibitory effect on the production of IL-4 and CXCL8 by NK and NKT-like cells than the effect of these drugs alone. Azithromycin 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 117-122 34414894-7 2021 Azithromycin suppressed production of IL-4 and CXCL8 by NK and NKT-like cells, and theophylline inhibited IL-4 synthesis by these lymphocytes. Azithromycin 0-12 C-X-C motif chemokine ligand 8 Homo sapiens 47-52 34414894-8 2021 The combination of azithromycin and budesonide had a more pronounced inhibitory effect on the production of IL-4 and CXCL8 by NK and NKT-like cells than the effect of these drugs alone. Budesonide 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 117-122 34414894-9 2021 The combination of theophylline and budesonide suppressed synthesis of IL-4 and CXCL8 by NK and NKT-like cells, as well as the production of TNFalpha and IFNgamma by NK cells stronger than budesonide alone. Theophylline 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 34203170-3 2021 We observed the secretion of inflammatory cytokines such as tumor necrosis factor-alpha (TNF-alpha), interleukin (IL)-6, and IL-8 by treating FLA-AA to human dermal fibroblasts, as well as macrophages. fla-aa 142-148 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 34414894-9 2021 The combination of theophylline and budesonide suppressed synthesis of IL-4 and CXCL8 by NK and NKT-like cells, as well as the production of TNFalpha and IFNgamma by NK cells stronger than budesonide alone. Budesonide 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 80-85 34106680-0 2021 Mid-Infrared Luminescence of the High Stability Perovskite CsPb1-xErxBr3-ZrF4-BaF2-LaF3-AlF3-NaF Fluoride Glass. Fluorides 97-105 C-X-C motif chemokine ligand 8 Homo sapiens 93-96 34212232-1 2021 This study aimed to formulate a hybrid coating material (HC) and to modify this HC with fluoride (NaF) and stannous (SnCl2) ions, directly or encapsulated in nano containers, testing the effects of these materials against dental erosion and erosion-abrasion. Fluorides 88-96 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 34372493-6 2021 Plasma IL-8, Ccl2, VEGF, and 8-isoprostane loaded onto one factor that was highest in the HIV+/METH+ group (p < 0.047) reflecting worse inflammation, vascular injury, and oxidative stress. Methamphetamine 95-99 C-X-C motif chemokine ligand 8 Homo sapiens 7-11 34234508-10 2021 Conclusion: We found that metabolites in phospholipid groups had strong associations with multiple inflammatory biomarkers, especially CRP, SAA and IL-8. Phospholipids 41-53 C-X-C motif chemokine ligand 8 Homo sapiens 148-152 34199005-11 2021 In contrast, an inflammatory response in A549 cells was more evident after exposure toward aerosols of nano-scaled filler combustion, whereas the thermal decomposition of PE-based materials revealed an impaired IL-8 secretion. Polyethylene 171-173 C-X-C motif chemokine ligand 8 Homo sapiens 211-215 34168274-8 2021 The hub targets for aspirin in preventing preeclampsia were tumor protein p53 (TP53), C-X-C motif chemokine ligand 8 (CXCL8), mitogen-activated protein kinase 3 (MAPK3), mitogen-activated protein kinase 1 (MAPK1), mitogen-activated protein kinase 14 (MAPK14), epidermal growth factor receptor (EGFR), estrogen receptor (ESR1), and prostaglandin-endoperoxide synthase 2 (PTGS2). Aspirin 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 86-116 34172787-9 2021 IL-8, alpha1AT, ferritin, CRP and LDH levels were higher in silicosis than in those exposed to silica without silicosis. Silicon Dioxide 95-101 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 34168274-8 2021 The hub targets for aspirin in preventing preeclampsia were tumor protein p53 (TP53), C-X-C motif chemokine ligand 8 (CXCL8), mitogen-activated protein kinase 3 (MAPK3), mitogen-activated protein kinase 1 (MAPK1), mitogen-activated protein kinase 14 (MAPK14), epidermal growth factor receptor (EGFR), estrogen receptor (ESR1), and prostaglandin-endoperoxide synthase 2 (PTGS2). Aspirin 20-27 C-X-C motif chemokine ligand 8 Homo sapiens 118-123 34284965-13 2022 CONCLUSION: Our work demonstrated that CXCL8 may be a potential molecule to be targeted for the treatment of PTX-resistant TNBC. Paclitaxel 109-112 C-X-C motif chemokine ligand 8 Homo sapiens 39-44 34284965-0 2022 CXCL8 Facilitates the Survival and Paclitaxel-Resistance of Triple-Negative Breast Cancers. Paclitaxel 35-45 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 34179086-5 2021 RT-qPCR was used to detect the mRNA expression of inflammatory cytokines (CCL2, IL-8, CCL4) and genes associated with angiogenesis (VEGF, ANG-1, ANG-2) in early EPCs after treatment of LPC (10 mug/ml) or phosphatidylcholine (PC, 10 mug/ml, control). Lysophosphatidylcholines 185-188 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 34284965-1 2022 BACKGROUND: This study aimed to demonstrate CXCL8 expression in TNBC tissues and cells, and elucidate the functional mechanism of CXCL8 in paclitaxel (PTX)-resistant TNBC. Paclitaxel 139-149 C-X-C motif chemokine ligand 8 Homo sapiens 44-49 34284965-1 2022 BACKGROUND: This study aimed to demonstrate CXCL8 expression in TNBC tissues and cells, and elucidate the functional mechanism of CXCL8 in paclitaxel (PTX)-resistant TNBC. Paclitaxel 139-149 C-X-C motif chemokine ligand 8 Homo sapiens 130-135 34284965-1 2022 BACKGROUND: This study aimed to demonstrate CXCL8 expression in TNBC tissues and cells, and elucidate the functional mechanism of CXCL8 in paclitaxel (PTX)-resistant TNBC. Paclitaxel 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 44-49 34284965-1 2022 BACKGROUND: This study aimed to demonstrate CXCL8 expression in TNBC tissues and cells, and elucidate the functional mechanism of CXCL8 in paclitaxel (PTX)-resistant TNBC. Paclitaxel 151-154 C-X-C motif chemokine ligand 8 Homo sapiens 130-135 34284965-5 2022 The protein expression and distribution of CXCL8 were examined by immunohistochemistry, MTT assay and colony formation assay were performed to determine cell viability of TNBC cells treated with PTX. Paclitaxel 195-198 C-X-C motif chemokine ligand 8 Homo sapiens 43-48 34284965-10 2022 CXCL8 was upregulated in PTX-resistant TNBC cells. Paclitaxel 25-28 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 34284965-11 2022 Knockdown of CXCL8 increased the sensitivity of TNBC cells to PTX. Paclitaxel 62-65 C-X-C motif chemokine ligand 8 Homo sapiens 13-18 34284965-12 2022 Mechanically, CXCL8 deficiency regulated PTX resistance in TNBC cells via cell apoptosis signaling pathway. Paclitaxel 41-44 C-X-C motif chemokine ligand 8 Homo sapiens 14-19 34234773-6 2021 Ultimately, one of the pathways through which CLEC12A regulates uric acid crystal-stimulated release of IL-8 by neutrophils is through a p38/PI3K-Akt signaling pathway. Uric Acid 64-73 C-X-C motif chemokine ligand 8 Homo sapiens 104-108 34204387-4 2021 18F-sodium fluoride (18F-NaF)-positron emission tomography (PET) is an emerging imaging modality with the potential for early diagnosis and monitoring of bone diseases through the detection of subtle metabolic changes. 18f-sodium fluoride 0-19 C-X-C motif chemokine ligand 8 Homo sapiens 25-28 34114445-0 2021 Effect of interferon combined with entecavir on serum IL-8, CRP and INF-gamma levels in patients with chronic hepatitis B. entecavir 35-44 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 34257799-14 2021 The concentrations of IL-1beta, IL-6, and IL-8 in the plasma were all decreased upon ZnO administration. Zinc Oxide 85-88 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 34177139-4 2021 CS is marked by elevated levels of inflammatory cytokines, mainly interleukin-6 (IL-6), IL-8, IL-10, tumour necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma). Cesium 0-2 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 34179086-5 2021 RT-qPCR was used to detect the mRNA expression of inflammatory cytokines (CCL2, IL-8, CCL4) and genes associated with angiogenesis (VEGF, ANG-1, ANG-2) in early EPCs after treatment of LPC (10 mug/ml) or phosphatidylcholine (PC, 10 mug/ml, control). Phosphatidylcholines 204-223 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 34179166-10 2021 Flu Avert treatment resulted in the modulation of IL-8, CCL2, and CXCL9 starting at days 5 and 6 post-treatment. flu avert 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 34204056-3 2021 The ellagitannins (1 and 2) were evaluated on its inhibitory activities of the enzyme 5alpha-reductase and tumor necrosis factor (TNF)-alpha, its interleukin (IL)-1beta, IL-6, and IL-8 production, and its anti-proliferation and apoptosis induction in prostate cells that show hypertrophy (RWPE-1 cell). Hydrolyzable Tannins 4-17 C-X-C motif chemokine ligand 8 Homo sapiens 180-184 34201243-6 2021 Quantitative RT-PCR analysis revealed that irinotecan at 15 microM was able to amplify the antiviral response (i.e., interferon-stimulated gene expression) of HSF exposed to PIC and reduce the expression of pro-inflammatory genes (CXCL8, IL-6 and COX-2) upon IL-1beta treatment. Irinotecan 43-53 C-X-C motif chemokine ligand 8 Homo sapiens 231-236 34108889-7 2021 iSN04 treatment recovered the deteriorated differentiation of plural DM myoblasts by downregulating myostatin and interleukin-8 (IL-8). isn04 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 114-127 34086734-0 2021 Dose- and time-dependent changes in viability and IL-6, CXCL8 and CCL2 production by HaCaT-cells exposed to cobalt. Cobalt 108-114 C-X-C motif chemokine ligand 8 Homo sapiens 56-61 34086734-12 2021 A linear mixed statistical model showed that cobalt exposure induces increase in IL-6, CXCL8 and CCL2 production over time and whereas increase of IL-6 and a decrease of CCL2 was associated with increasing cobalt chloride concentrations. Cobalt 45-51 C-X-C motif chemokine ligand 8 Homo sapiens 87-92 34082514-0 2021 Incidental Skeletal Findings on Sodium-fluoride Positron Emission Tomography: A Collection of Benign Tumors Sodium-fluoride (NaF) positron emission tomography (PET) is a sensitive method to detect altered bone mineralization. Sodium Fluoride 32-47 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 34082514-0 2021 Incidental Skeletal Findings on Sodium-fluoride Positron Emission Tomography: A Collection of Benign Tumors Sodium-fluoride (NaF) positron emission tomography (PET) is a sensitive method to detect altered bone mineralization. Sodium Fluoride 108-123 C-X-C motif chemokine ligand 8 Homo sapiens 125-128 32890135-10 2021 BOS with lower CCSP also induced Interleukin-8 and reduced vascular endothelial growth factor. N-[4-(Aminosulfonyl)phenyl]-2-Mercaptobenzamide 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 33-46 34082668-11 2021 CONCLUSION: MMP2, CXCL8, PIK3R3, ITGB3, and LEF1 may play roles in the efficacy of vemurafenib treatment in melanoma; for example, MMP2 and PIK3R3 are likely associated with vemurafenib resistance. Vemurafenib 83-94 C-X-C motif chemokine ligand 8 Homo sapiens 18-23 34114392-6 2021 RESULTS: The results showed that BYF, BJF and YZF treatment strongly decreased the CSE-induced secretion of interleukin (IL)-6, IL-8, tumor necrosis factor-alpha and matrix metalloproteinase-9 by THP-1 cells. bjf 38-41 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 34114392-6 2021 RESULTS: The results showed that BYF, BJF and YZF treatment strongly decreased the CSE-induced secretion of interleukin (IL)-6, IL-8, tumor necrosis factor-alpha and matrix metalloproteinase-9 by THP-1 cells. yzf 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 33577242-8 2021 With a BG concentration of 2.5%, IL-6 and IL-8 concentrations were smaller compared with the control group without BG after 2 days" incubation. O(6)-benzylguanine 7-9 C-X-C motif chemokine ligand 8 Homo sapiens 42-46 34108889-7 2021 iSN04 treatment recovered the deteriorated differentiation of plural DM myoblasts by downregulating myostatin and interleukin-8 (IL-8). isn04 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 129-133 34063134-0 2021 Interleukin-6 and Interleukin-8 Regulate STAT3 Activation Migration/Invasion and EMT in Chrysophanol-Treated Oral Cancer Cell Lines. chrysophanic acid 88-100 C-X-C motif chemokine ligand 8 Homo sapiens 18-31 34071008-0 2021 Allicin Could Potentially Alleviate Oral Cancer Pain by Inhibiting "Pain Mediators" TNF-alpha, IL-8, and Endothelin. allicin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 34071008-6 2021 Allicin inhibited both gene and protein expression of TNF-alpha, IL-8, and endothelin in both cancer cells and cancer stem cells. allicin 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 34093525-4 2021 Using human monocyte/macrophage-like Thp-1 cells and human primary monocytes and macrophages, we were able to determine that a substantial part of early phagocytic cell activation, including NF-kappaB activation and IL-8 production, by live H. pylori is triggered by bacterial heptose metabolites. Heptoses 277-284 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 34063134-6 2021 However, the effect of chrysophanol on the production of IL-6 and IL-8 is unknown. chrysophanic acid 23-35 C-X-C motif chemokine ligand 8 Homo sapiens 66-70 34063134-9 2021 Our results showed that treatment with chrysophanol significantly decreased the expression of IL-6 and IL-8, as well as the invasion ability of oral cancer cells. chrysophanic acid 39-51 C-X-C motif chemokine ligand 8 Homo sapiens 103-107 34063134-11 2021 Mechanistically, chrysophanol inhibited IL-6- and IL-8-induced invasion and STAT3 phosphorylation. chrysophanic acid 17-29 C-X-C motif chemokine ligand 8 Homo sapiens 50-54 34602387-5 2021 The mRNA expression of TNF-alpha, IL-8 and IL-1beta in the azithromycin group was lower than that in the control group (P<0.05). Azithromycin 59-71 C-X-C motif chemokine ligand 8 Homo sapiens 34-38 34173106-4 2021 HUVEC cells cultured in the presence of high glucose concentration (30 mmol/ml) and treated with CXCL8 (50 ng/ml) demonstrated more intensive proliferation, migration, and p-ERK/ERK, p-P38/P38, and p-JNK/JNK ratios and significantly lower apoptosis rate than control cells (high glucose, no treatment) and cells treated with CXCL8 and transfected with microRNA-126-mimic. Glucose 45-52 C-X-C motif chemokine ligand 8 Homo sapiens 97-102 34084299-7 2021 Patients with abnormal DMSA had significantly higher serum IL-6 and IL-8 compared with those with normal DMSA scan (187.1 +- 113.1 ng/mL vs. 396.1 +- 246.0 ng/mL, P = 0.005; and 165 +- 76.1 ng/mLvs. Succimer 23-27 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 35513145-11 2022 Exposure of cells to large PS particles (500-5000 nm) upregulated interleukin-8 and the effect was enhanced at 24 h. Overall, the study demonstrated that smaller aminated particles were most toxic to hepatocytes, but larger particles induced apoptotic cell death or an inflammatory response depending on the length of exposure. Phosphorus 27-29 C-X-C motif chemokine ligand 8 Homo sapiens 66-79 34981477-0 2021 The Role of Chemokines in Cardiovascular Diseases and the Therapeutic Effect of Curcumin on CXCL8 and CCL2 as Pathological Chemokines in Atherosclerosis. Curcumin 80-88 C-X-C motif chemokine ligand 8 Homo sapiens 92-97 34237749-10 2021 The presence of the copper ions prevented the dramatic increase of pro-inflammatory cytokines (interleukin (IL)-6 and IL-8) and transforming growth factor beta-1 that followed skin burning. Copper 20-26 C-X-C motif chemokine ligand 8 Homo sapiens 118-122 35489096-3 2022 With the first platform, the recognition layer consisted with immobilised IL-8 on aminothiol modified gold electrodes. Aminothiol 82-92 C-X-C motif chemokine ligand 8 Homo sapiens 74-78 35398417-4 2022 Here, we evaluated the associations between PM10, NO2 and O3 exposure (on the day of the blood sample collection and on the day before, and the mean annual residential level) and levels of the inflammatory biomarkers high-sensitivity C-reactive protein (hsCRP), interleukin (IL)-1beta, IL-6, IL-8, IL-10, IL-17A, IL-22, and tumor necrosis factor alpha. pm10 44-48 C-X-C motif chemokine ligand 8 Homo sapiens 292-296 35489096-7 2022 A side-by-side comparison showed that aminothiol/activated MWCNTs/anti-IL-8 based impedimetric immunosensor exhibits high reproducibility (The relative standard deviation (R.S.D) = 3.2%, n = 3) with high stability. Aminothiol 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 71-75 35537534-3 2022 Then, the synergistic effects of NaF nanoparticles and DCV on adhesive performance were studied in terms of fluoride (F-) ion release, antibacterial activity, hydrophilicity, surface potential, cytotoxicity, and bonding strength. Fluorides 108-116 C-X-C motif chemokine ligand 8 Homo sapiens 33-36 35452830-12 2022 CONCLUSION: CRRT with topical citrate + low-dose LMW heparin-calcium anticoagulation in the treatment of patients with SAP reduces the levels of WBC, CRP, and PCT and the concentrations of cytokines, including IL-6, IL-8, and TNF-alpha. Citric Acid 30-37 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 35452830-12 2022 CONCLUSION: CRRT with topical citrate + low-dose LMW heparin-calcium anticoagulation in the treatment of patients with SAP reduces the levels of WBC, CRP, and PCT and the concentrations of cytokines, including IL-6, IL-8, and TNF-alpha. Calcium 61-68 C-X-C motif chemokine ligand 8 Homo sapiens 216-220 35599022-6 2022 Microvessels exhibited physiological relevant trans-endothelial electrical resistance (TEER), were leak-tight for 10 kDa dextran-Alexa 647 and strongly limited the permeability of sodium fluorescein (NaF). Fluorescein 180-198 C-X-C motif chemokine ligand 8 Homo sapiens 200-203 35537534-1 2022 OBJECTIVE: Aiming to achieve improved antibacterial performance for dental application, sodium fluoride (NaF) nanoparticles and photopolymerizable N,N-dodecylvinylimidazole (DCV) were co-introduced into resin adhesives at different ratios. Sodium Fluoride 88-103 C-X-C motif chemokine ligand 8 Homo sapiens 105-108 35352237-6 2022 Furthermore, quercetin decreased the pro-inflammatory cell environment upon LPS-induced endothelial activation, in terms of tumor necrosis factor- alpha (TNF-alpha), interleukin-6 (IL-6), interleukin-8 (IL-8), and sVCAM-1 expression. Quercetin 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 188-201 35352237-6 2022 Furthermore, quercetin decreased the pro-inflammatory cell environment upon LPS-induced endothelial activation, in terms of tumor necrosis factor- alpha (TNF-alpha), interleukin-6 (IL-6), interleukin-8 (IL-8), and sVCAM-1 expression. Quercetin 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 203-207 35537534-5 2022 The cationic quaternary ammonium group could reduce the burst release of negative F- ion for the adhesive at a NaF/DCV ratio (1:1, 2 wt%), hence achieving both non-contact and contact antibacterial activity in an extended term without causing cytotoxicity. quaternary ammonium 13-32 C-X-C motif chemokine ligand 8 Homo sapiens 111-114 35384906-10 2022 Recently, 18F-sodium fluoride (NaF) has been used for detection and quantification of molecular calcification in the plaques. 18f-sodium fluoride 10-29 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 34991200-0 2022 Effect of long-chain inorganic polyphosphate treated with wheat phytase on IL-8 signaling in HT-29 cells. Polyphosphates 31-44 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 34991200-1 2022 Objective: This study was performed to investigate the potential effect of wheat phytase on long-chain inorganic polyphosphate (polyP)-mediated IL-8 signaling in an intestinal epithelial cell line, HT-29 cells. Polyphosphates 113-126 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34991200-1 2022 Objective: This study was performed to investigate the potential effect of wheat phytase on long-chain inorganic polyphosphate (polyP)-mediated IL-8 signaling in an intestinal epithelial cell line, HT-29 cells. Polyphosphates 128-133 C-X-C motif chemokine ligand 8 Homo sapiens 144-148 34991200-6 2022 Moreover, the 24 h exposure of cells to enzyme-treated 50 mM polyP1150 reduced the secretion of IL-8 and the activation of NF-kB by 9 and 19%, respectively, compared to the intact substrate. polyp1150 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 35452996-7 2022 Evaluation of the cell death phenotype revealed that glutaminolysis inhibitory treatment with CB839 or a low-glutamine medium significantly promoted the proliferation of beta-galactosidase-positive and IL-6/IL-8 secretory cells among X-irradiated tumor cells, corresponding to an increase in the senescent cell population. CB-839 94-99 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 35452996-7 2022 Evaluation of the cell death phenotype revealed that glutaminolysis inhibitory treatment with CB839 or a low-glutamine medium significantly promoted the proliferation of beta-galactosidase-positive and IL-6/IL-8 secretory cells among X-irradiated tumor cells, corresponding to an increase in the senescent cell population. Glutamine 109-118 C-X-C motif chemokine ligand 8 Homo sapiens 207-211 35170144-10 2022 Sputum inflammatory markers interleukin-1beta (P < 0.001), interleukin-8 (P < 0.001) and tumour necrosis factor-alpha (P = 0.003) were lower with gentamicin. Gentamicins 146-156 C-X-C motif chemokine ligand 8 Homo sapiens 59-72 35623041-0 2022 Signaling via dopamine and adenosine receptors modulate viral peptide-specific and T-cell IL-8 response in COVID-19. Dopamine 14-22 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 35623041-0 2022 Signaling via dopamine and adenosine receptors modulate viral peptide-specific and T-cell IL-8 response in COVID-19. Adenosine 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 35623041-6 2022 We have found that (i) patients show marked IL-8 but not IL-17A responses; (ii) these responses are restricted by HLA-DR; and (iii) IL-8 responses are abrogated by a dopamine D2 like receptor (D2R) agonist, ropinirole, and an adenosine A2a receptor (A2aR) antagonist, istradefylline. Dopamine 166-174 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 35623041-6 2022 We have found that (i) patients show marked IL-8 but not IL-17A responses; (ii) these responses are restricted by HLA-DR; and (iii) IL-8 responses are abrogated by a dopamine D2 like receptor (D2R) agonist, ropinirole, and an adenosine A2a receptor (A2aR) antagonist, istradefylline. ropinirole 207-217 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 35623041-6 2022 We have found that (i) patients show marked IL-8 but not IL-17A responses; (ii) these responses are restricted by HLA-DR; and (iii) IL-8 responses are abrogated by a dopamine D2 like receptor (D2R) agonist, ropinirole, and an adenosine A2a receptor (A2aR) antagonist, istradefylline. istradefylline 268-282 C-X-C motif chemokine ligand 8 Homo sapiens 132-136 35605724-10 2022 Copper exposure stimulated 16HBE cells to release proinflammatory IL-6 and IL-8. Copper 0-6 C-X-C motif chemokine ligand 8 Homo sapiens 75-79 35603939-11 2022 In HCT116 cells, tunicamycin increased the expression of Grp78, Gro-alpha and IL-8 in a concentration-dependent manner. Tunicamycin 17-28 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 35603939-12 2022 Furthermore, p38 MAPK inhibitor significantly inhibited the upregulation of Gro-alpha and IL-8 induced by tunicamycin. Tunicamycin 106-117 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 35631467-8 2022 Further analysis of unique compounds found in A. dracunculus showed that farnesene, a compound with a similar hydrocarbon structure as lipoxin A4, inhibited Ca2+ influx induced in human neutrophils by fMLF (IC50 = 1.2 muM), WKYMVM (IC50 = 1.4 muM), or interleukin 8 (IC50 = 2.6 muM). Sesquiterpenes 73-82 C-X-C motif chemokine ligand 8 Homo sapiens 252-265 35589610-0 2022 Ladarixin, an inhibitor of IL-8 receptors CXCR1 and CXCR2, in new-onset type 1 diabetes: a multicenter, randomized, double-blind, placebo-controlled trial. 2'-((4'-trifluoromethanesulfonyloxy)phenyl)-N-methanesulfonylpropionamide 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 27-31 35631269-2 2022 In this study, the ability to regulate the production of IL-8 of the water-soluble non-starch polysaccharide (WS-NSP) from taro corm (Tc-WS-NSP) extracted using a conventional (CE) or improved conventional (ICE) extraction method, of the probiotics Lactobacillus acidophilus, Bifidobacterium breve, and Bifidobacterium infantis, and their synbiotic mixtures were evaluated. ws-nsp 110-116 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 35631269-2 2022 In this study, the ability to regulate the production of IL-8 of the water-soluble non-starch polysaccharide (WS-NSP) from taro corm (Tc-WS-NSP) extracted using a conventional (CE) or improved conventional (ICE) extraction method, of the probiotics Lactobacillus acidophilus, Bifidobacterium breve, and Bifidobacterium infantis, and their synbiotic mixtures were evaluated. Water 69-74 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 35631269-2 2022 In this study, the ability to regulate the production of IL-8 of the water-soluble non-starch polysaccharide (WS-NSP) from taro corm (Tc-WS-NSP) extracted using a conventional (CE) or improved conventional (ICE) extraction method, of the probiotics Lactobacillus acidophilus, Bifidobacterium breve, and Bifidobacterium infantis, and their synbiotic mixtures were evaluated. Tungsten 137-139 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 35631269-2 2022 In this study, the ability to regulate the production of IL-8 of the water-soluble non-starch polysaccharide (WS-NSP) from taro corm (Tc-WS-NSP) extracted using a conventional (CE) or improved conventional (ICE) extraction method, of the probiotics Lactobacillus acidophilus, Bifidobacterium breve, and Bifidobacterium infantis, and their synbiotic mixtures were evaluated. Starch 87-93 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 35631269-5 2022 The ability demonstrated by the Tc-WS-NSPs, the probiotics, and their synbiotics mixtures to downregulate IL-8 production in the presence of an NEC-positive-associated pathogen may be useful in the development of novel prophylactic agents against NEC. tc-ws 32-37 C-X-C motif chemokine ligand 8 Homo sapiens 106-110 35631269-2 2022 In this study, the ability to regulate the production of IL-8 of the water-soluble non-starch polysaccharide (WS-NSP) from taro corm (Tc-WS-NSP) extracted using a conventional (CE) or improved conventional (ICE) extraction method, of the probiotics Lactobacillus acidophilus, Bifidobacterium breve, and Bifidobacterium infantis, and their synbiotic mixtures were evaluated. Polysaccharides 94-108 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 35570777-9 2022 The relationships of IL-6 and IL-8 in ME/CFS and S-ME/CFS participants also differed from Cs. 2-(N-morpholino)ethanesulfonic acid 49-53 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 35503917-4 2022 A pathway to obtain single crystals was shown by growing NaSrY(BO3)2 and NaSrYb(BO3)2 by the top seeded solution growth method with Na2O-B2O3-NaF flux. sodium oxide 132-136 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 35589431-1 2022 AIM: To investigate if the pattern of fluorine-18-labelled sodium fluoride (18F-NaF) uptake on integrated positron-emission tomography (PET)/magnetic resonance imaging (MRI) of bone marrow lesions (BML) and osteophytes differs between different knee compartments. Fluorine 38-46 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 35589431-1 2022 AIM: To investigate if the pattern of fluorine-18-labelled sodium fluoride (18F-NaF) uptake on integrated positron-emission tomography (PET)/magnetic resonance imaging (MRI) of bone marrow lesions (BML) and osteophytes differs between different knee compartments. Sodium Fluoride 59-74 C-X-C motif chemokine ligand 8 Homo sapiens 80-83 35503917-4 2022 A pathway to obtain single crystals was shown by growing NaSrY(BO3)2 and NaSrYb(BO3)2 by the top seeded solution growth method with Na2O-B2O3-NaF flux. boron oxide 137-141 C-X-C motif chemokine ligand 8 Homo sapiens 142-145 35574627-8 2022 Also, curcumin supplementation elicited significant improvements in MVC (WMD = 3.10 nm, 95% CI (1.45-4.75)) and ROM (WMD = 6.49 , 95% CI (3.91-9.07)), although no significant changes in IL-6 and IL-8 levels were found. Curcumin 6-14 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 35576915-11 2022 CONCLUSION: Our results show that active tVNS led to an immediate increase in the serum concentrations of certain pro-inflammatory cytokines such as IL-1beta, IL-6, and/or IL-8 in two independent cohorts of healthy study participants. tvns 41-45 C-X-C motif chemokine ligand 8 Homo sapiens 172-176 35625855-7 2022 In RASF, THC (>=5 microM) increased intracellular calcium levels/PoPo3 uptake in a TRPA1-dependent manner and reduced interleukin-8 (IL-8) and matrix metalloprotease 3 (MMP-3) production at high concentrations (25 microM). Dronabinol 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 118-131 35570014-1 2022 OBJECTIVES: The objectives of this study were to compare the amount of fluoride delivered via a topical application of 38% silver diamine fluoride (SDF) solution and 5% sodium fluoride (NaF) varnish as well as to determine the amount of 38% SDF solution delivered using various micro-applicators. Fluorides 71-79 C-X-C motif chemokine ligand 8 Homo sapiens 186-189 35570014-1 2022 OBJECTIVES: The objectives of this study were to compare the amount of fluoride delivered via a topical application of 38% silver diamine fluoride (SDF) solution and 5% sodium fluoride (NaF) varnish as well as to determine the amount of 38% SDF solution delivered using various micro-applicators. Sodium Fluoride 169-184 C-X-C motif chemokine ligand 8 Homo sapiens 186-189 35570014-2 2022 METHODS: The weights of 38% SDF (Saforide) and 5% NaF (Duraphat) applied to the occlusal surface of an extracted human upper first premolar with a regular-size (2.50-mm tip diameter) micro-applicator were measured using an electronic-analytical balance. sodium fluoride topical preparation 55-63 C-X-C motif chemokine ligand 8 Homo sapiens 50-53 35570014-6 2022 RESULTS: The mean weights of the fluoride delivered via the SDF solution and NaF varnish were 0.25 +- 0.07 mg and 0.49 +- 0.08 mg, respectively (P < .001). Fluorides 33-41 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 35625855-7 2022 In RASF, THC (>=5 microM) increased intracellular calcium levels/PoPo3 uptake in a TRPA1-dependent manner and reduced interleukin-8 (IL-8) and matrix metalloprotease 3 (MMP-3) production at high concentrations (25 microM). Dronabinol 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 133-137 35570279-5 2022 RESULTS: HRV-Cs infect and propagate in fully differentiated HBE cells and significantly increase the secretion of IFN-lambda1, CCL5, IP10, IL-6, IL-8, and MCP-1. hrv-cs 9-15 C-X-C motif chemokine ligand 8 Homo sapiens 146-150 35570014-0 2022 Fluoride Delivered via a Topical Application of 38% SDF and 5% NaF. Fluorides 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 35546010-0 2022 Ozone improved the wound healing in type 2 diabetics via down-regulation of IL- 8, 10 and induction of FGFR expression. Ozone 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 76-81 35521772-10 2022 The concentrations of follicular IL-6, IL-8 and mature IL-18 were significantly higher in PCOS group and were positively correlated with the levels of fatty acids. Fatty Acids 151-162 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 35624784-4 2022 CDCA treatment provoked ROS production, followed by IL-8 and ICAM-1 expression in hepatocytes within 8 h, which accelerated 24 h post-treatment. Chenodeoxycholic Acid 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 52-56 35624784-7 2022 In contrast, SP treatment reduced ROS production and blocked IL-8/ICAM-1 in CDCA-injured hepatocytes. Chenodeoxycholic Acid 76-80 C-X-C motif chemokine ligand 8 Homo sapiens 61-65 35535007-10 2022 IL-8 concentration in cultures stimulated with talc and adenocarcinoma supernatant was higher compared to cultures stimulated with talc only. Talc 47-51 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 35521772-11 2022 Moreover, oleic acid stimulation upregulated the transcription levels of IL-6 and IL-8 via ERK1/2 signaling pathways in KGN cells. Oleic Acid 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 82-86 35600871-11 2022 Additionally, TNF-alpha-induced IL-8 production in BEAS-2B cells was not completely inhibited by Dex, while R406 markedly promoted the anti-inflammatory effect of Dex. Dexamethasone 97-100 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 35600871-11 2022 Additionally, TNF-alpha-induced IL-8 production in BEAS-2B cells was not completely inhibited by Dex, while R406 markedly promoted the anti-inflammatory effect of Dex. Dexamethasone 163-166 C-X-C motif chemokine ligand 8 Homo sapiens 32-36 35315502-4 2022 In the present study, the efficacy of co-targeting IL-6 and IL-8 in human ovarian cancer cells by bazedoxifene (Baze) + SCH527123 (SCH) treatment was examined. bazedoxifene 98-110 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 35571237-5 2022 In vitro, miR-150-5p overexpression decreased the contents of inflammatory factors interleukin- (IL-) 6, IL-8 along with cyclooxygenase-2 (COX-2), and endoplasmic reticulum (ER) stress markers glucose-regulated protein (GRP) 78 and C/-EBP homologous protein (CHOP) and promoted cell migrate. mir-150-5p 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 35247648-5 2022 There are four cysteine residues forming two disulfide linkage and 14 basic amino acid residues which result in a very basic property for the binding of IL-8 to heparan sulfate-proteoglycan. Cysteine 15-23 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 35247648-5 2022 There are four cysteine residues forming two disulfide linkage and 14 basic amino acid residues which result in a very basic property for the binding of IL-8 to heparan sulfate-proteoglycan. Disulfides 45-54 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 35247648-5 2022 There are four cysteine residues forming two disulfide linkage and 14 basic amino acid residues which result in a very basic property for the binding of IL-8 to heparan sulfate-proteoglycan. Amino Acids, Basic 70-86 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 35247648-5 2022 There are four cysteine residues forming two disulfide linkage and 14 basic amino acid residues which result in a very basic property for the binding of IL-8 to heparan sulfate-proteoglycan. Heparitin Sulfate 161-176 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 35278812-7 2022 Nitrites significantly correlated with IL-8 during relapse. Nitrites 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 35421827-3 2022 Using Sprague-Dawley rats exposed to sodium fluoride (NaF) from gestation through delivery until the neonatal offspring reached six months of age as an in vivo model. Sodium Fluoride 37-52 C-X-C motif chemokine ligand 8 Homo sapiens 54-57 35421827-8 2022 Mechanistically, V-ATPase B2 overexpression and ATP effectively restored V-ATPase expression, reducing NaF-induced lysosomal alkalinization while increasing lysosomal degradation capacity. Adenosine Triphosphate 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 103-106 35412656-9 2022 Additionally, ectoine reduces production of AREG and interleukin-8 by CF primary bronchial epithelial cells. ectoine 14-21 C-X-C motif chemokine ligand 8 Homo sapiens 53-66 34989247-8 2022 We propose that sample tubes containing NaF-EDTA-citrate be used for the measurement of uric acid in patients administered rasburicase. Uric Acid 88-97 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 35506423-6 2022 Secondly, Everolimus significantly reduced the expressions of the pro-inflammatory cytokines interleukin (IL)-6, tumor necrosis factor-alpha (TNF-alpha), and IL-8. Everolimus 10-20 C-X-C motif chemokine ligand 8 Homo sapiens 158-162 35429917-9 2022 RESULTS: In LMM, a two-fold increase in urinary cesium (Cs) and chromium (Cr) was statistically associated with -35.22% (95% confidence interval (CI): -53.17, -10.40) changes in interleukin 6 (IL-6) and -11.13% (95 %CI: -20.67, -0.44) in IL-8. Cesium 48-54 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 35429917-9 2022 RESULTS: In LMM, a two-fold increase in urinary cesium (Cs) and chromium (Cr) was statistically associated with -35.22% (95% confidence interval (CI): -53.17, -10.40) changes in interleukin 6 (IL-6) and -11.13% (95 %CI: -20.67, -0.44) in IL-8. Cesium 56-58 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 35429917-9 2022 RESULTS: In LMM, a two-fold increase in urinary cesium (Cs) and chromium (Cr) was statistically associated with -35.22% (95% confidence interval (CI): -53.17, -10.40) changes in interleukin 6 (IL-6) and -11.13% (95 %CI: -20.67, -0.44) in IL-8. Chromium 64-72 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 35429917-9 2022 RESULTS: In LMM, a two-fold increase in urinary cesium (Cs) and chromium (Cr) was statistically associated with -35.22% (95% confidence interval (CI): -53.17, -10.40) changes in interleukin 6 (IL-6) and -11.13% (95 %CI: -20.67, -0.44) in IL-8. Chromium 74-76 C-X-C motif chemokine ligand 8 Homo sapiens 238-242 35315502-4 2022 In the present study, the efficacy of co-targeting IL-6 and IL-8 in human ovarian cancer cells by bazedoxifene (Baze) + SCH527123 (SCH) treatment was examined. bazedoxifene 112-116 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 35315502-4 2022 In the present study, the efficacy of co-targeting IL-6 and IL-8 in human ovarian cancer cells by bazedoxifene (Baze) + SCH527123 (SCH) treatment was examined. 2-hydroxy-N,N-dimethyl-3-(2-((1-(5-methylfuran-2-yl)propyl)amino)-3,4-dioxocyclobut-1-enylamino)benzamide 120-129 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 35315502-4 2022 In the present study, the efficacy of co-targeting IL-6 and IL-8 in human ovarian cancer cells by bazedoxifene (Baze) + SCH527123 (SCH) treatment was examined. 2-hydroxy-N,N-dimethyl-3-(2-((1-(5-methylfuran-2-yl)propyl)amino)-3,4-dioxocyclobut-1-enylamino)benzamide 131-134 C-X-C motif chemokine ligand 8 Homo sapiens 60-64 35315502-8 2022 Compared with the DMSO control, the combination of IL-6/glycoprotein 130 inhibitor Baze and IL-8 inhibitor SCH synergistically inhibited cell viability in ovarian cancer cells. 2-hydroxy-N,N-dimethyl-3-(2-((1-(5-methylfuran-2-yl)propyl)amino)-3,4-dioxocyclobut-1-enylamino)benzamide 107-110 C-X-C motif chemokine ligand 8 Homo sapiens 92-96 35437207-7 2022 RESULTS: EKH significantly induced IL-6 and IL-8 in NHDF and HMVEC-dBl. 5-Chlorotubercidin 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 44-48 35403296-9 2022 After vitamin D supplementation for 90 days, T2DM patients had a 2-fold increase of GSH levels, from 2.72 +- 0.84 to 5.76 +- 3.19 mumol/ml, the concentration of MCP-1 decreased from 51.11 +- 20.86 to 25.42 +- 13.06 pg/ml, and IL-8 also decreased from 38.21 +- 21.76 to 16.05 +- 8.99 pg/ml. Vitamin D 6-15 C-X-C motif chemokine ligand 8 Homo sapiens 226-230 35403296-10 2022 In conclusion, our study demonstrated that vitamin D could regulate the production of GSH, thereby reducing the serum levels of MCP-1 and IL-8, alleviating oxidative stress and inflammation, providing evidence of the necessity and feasibility of adjuvant vitamin D treatment among patients with T2DM. Vitamin D 43-52 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 35150143-6 2022 White blood cells, neutrophils, platelets, erythrocyte sedimentation rate (ESR), and the levels of interleukin-8 significantly decreased in the nano-curcumin group compared to the placebo after 10 days of intervention (p = .024, p = .045, p = .017, p = .041, and p = .004, respectively). Curcumin 149-157 C-X-C motif chemokine ligand 8 Homo sapiens 99-112 35150143-16 2022 For the first time, this trial was conducted to determine the effect of nano-curcumin on hematological indices and the serum levels of presepsin and IL-8. nano-curcumin 72-85 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 35487914-6 2022 IL8-targeted by RNA interference or reparixin reversed chemotherapy resistance with limited toxicity in vivo and vitro experiments. reparixin 36-45 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 35306372-3 2022 Photochemical oxidation of isoprene leads to the formation of hydroperoxides, environmental oxidants that lead to inflammatory (IL-8) and adaptive (HMOX1) gene expression in human airway epithelial cells (HAEC). isoprene 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 35306372-3 2022 Photochemical oxidation of isoprene leads to the formation of hydroperoxides, environmental oxidants that lead to inflammatory (IL-8) and adaptive (HMOX1) gene expression in human airway epithelial cells (HAEC). Hydrogen Peroxide 62-76 C-X-C motif chemokine ligand 8 Homo sapiens 128-132 35563819-10 2022 The infiltration of T cells into the epidermis was reduced when ALA was added to the culture medium, and significant decreases in the levels of inflammatory cytokines and chemokines such as CXCL1, interleukin-6 (IL-6) and interleukin-8 (IL-8) were consequently measured in psoriatic substitutes supplemented with this n-3 PUFA. alpha-Linolenic Acid 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 222-235 35563819-10 2022 The infiltration of T cells into the epidermis was reduced when ALA was added to the culture medium, and significant decreases in the levels of inflammatory cytokines and chemokines such as CXCL1, interleukin-6 (IL-6) and interleukin-8 (IL-8) were consequently measured in psoriatic substitutes supplemented with this n-3 PUFA. alpha-Linolenic Acid 64-67 C-X-C motif chemokine ligand 8 Homo sapiens 237-241 35352794-8 2022 ER stress inducer significantly increased while ER stress inhibitor TUDCA significantly decreased the expression and secretion of TNF-alpha, IL-1beta and IL-8 in THP-1 cells treated by LPS. ursodoxicoltaurine 68-73 C-X-C motif chemokine ligand 8 Homo sapiens 154-158 35352794-10 2022 Furthermore, p38 inhibitor SB203580 inhibited the production and secretion of TNF-alpha, IL-1beta and IL-8 in THP-1 cells treated with LPS. SB 203580 27-35 C-X-C motif chemokine ligand 8 Homo sapiens 102-106 35563797-9 2022 Six months after completion of the BPA treatment, there was a decrease in concentrations of IL-6 ( = -1.61 (-3.11; -0.20); p = 0.03), of IL8 ( = -3.24 (-7.72; 0.82); p = 0.01), and of ET-1 ( = -0.47 (-0.96; 0.05); p = 0.005). bisphenol A 35-38 C-X-C motif chemokine ligand 8 Homo sapiens 138-141 35216930-1 2022 OBJECTIVES: The aim of this study was to describe the potential of 18F-sodium fluoride (18F-NaF) positron emission tomography (PET) to identify graft vasculopathy and to investigate the influence of coronary artery bypass graft (CABG) surgery on native coronary artery disease activity and progression. 18f-sodium fluoride 67-86 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 35509603-15 2022 HIF-1a stimulation by dimethyloxalylglycine (DMOG) could restore IL-8 secretion in SLC16A3 downregulated cells. oxalylglycine 22-43 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 35509603-15 2022 HIF-1a stimulation by dimethyloxalylglycine (DMOG) could restore IL-8 secretion in SLC16A3 downregulated cells. oxalylglycine 45-49 C-X-C motif chemokine ligand 8 Homo sapiens 65-69 35199431-6 2022 As proven, weak ion solvation/desolvation of tetrahydrofuran greatly facilitates fast-ion diffusion at the SEI/electrolyte interface and homogeneous SEI with well-distributed NaF and organic components ensures fast Na+ diffusion through the SEI layer and a stable interface. tetrahydrofuran 45-60 C-X-C motif chemokine ligand 8 Homo sapiens 175-178 35443035-7 2022 Moreover, ATP and ADP were significantly positively correlated with the Positive and Negative Symptom Scale (PANSS) item "lack of judgment and insight"; IL-1beta, IL-12 and TNF-alpha were significantly positively correlated with "tension" and "depression"; and "disorientation" and "poor attention" were correlated significantly with IL-6 and IL-8. Adenosine Triphosphate 10-13 C-X-C motif chemokine ligand 8 Homo sapiens 343-347 35509853-9 2022 Additionally, miR-141-3p could reduce IL-6 and IL-8. mir-141-3p 14-24 C-X-C motif chemokine ligand 8 Homo sapiens 47-51 35593365-12 2022 The results indicated that quercetin and wogonin had better affinity with CXCL8, CCL2 or IL1B. Quercetin 27-36 C-X-C motif chemokine ligand 8 Homo sapiens 74-79 35593365-12 2022 The results indicated that quercetin and wogonin had better affinity with CXCL8, CCL2 or IL1B. wogonin 41-48 C-X-C motif chemokine ligand 8 Homo sapiens 74-79 35593365-14 2022 The expression CXCL8, CCL2 or IL1B were down-regulated after quercetin or wogonin treating, compared with LPS-induced A549 cells (P < 0.01). Quercetin 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 35593365-14 2022 The expression CXCL8, CCL2 or IL1B were down-regulated after quercetin or wogonin treating, compared with LPS-induced A549 cells (P < 0.01). wogonin 74-81 C-X-C motif chemokine ligand 8 Homo sapiens 15-20 35441257-2 2022 Nicotine has been shown to stimulate the production of cytokines that are priming agents for inflammation that induces tissue destruction, such as IL-1beta, IL-6, and IL-8, by gingival keratinocytes and human gingival fibroblasts (HGF). Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 35441257-8 2022 Nicotine elevated the expression of pro-inflammatory cytokines TNF-alpha, IL-1beta, IL-6, IL-8, and IL-17 and decreased the anti-inflammatory IL-10 in HGFs at 24 and 72 h. Boric acid at 100 ng/mL in the medium prevented the changes induced by nicotine alone. Nicotine 0-8 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 35563697-10 2022 Our multiplex ELISA data revealed that CBD and THC significantly diminished the levels of IL-6, IL-8, and tumor necrosis factor-alpha (TNF-alpha) after LPS treatment in THP-1 macrophages and HBECs. Cannabidiol 39-42 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 35563697-10 2022 Our multiplex ELISA data revealed that CBD and THC significantly diminished the levels of IL-6, IL-8, and tumor necrosis factor-alpha (TNF-alpha) after LPS treatment in THP-1 macrophages and HBECs. Dronabinol 47-50 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 35460727-9 2022 Increased uric acid levels were positively correlated with mucosal neutrophil numbers and IFN-gamma, IL-17A, IL-1beta, and IL-8 mRNA levels. Uric Acid 10-19 C-X-C motif chemokine ligand 8 Homo sapiens 123-127 35443035-7 2022 Moreover, ATP and ADP were significantly positively correlated with the Positive and Negative Symptom Scale (PANSS) item "lack of judgment and insight"; IL-1beta, IL-12 and TNF-alpha were significantly positively correlated with "tension" and "depression"; and "disorientation" and "poor attention" were correlated significantly with IL-6 and IL-8. Adenosine Diphosphate 18-21 C-X-C motif chemokine ligand 8 Homo sapiens 343-347 35460727-13 2022 Glutathione treatment reduced IL-8 mRNA expression in cultured nasal polyp tissues. Glutathione 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 35456686-7 2022 Furthermore, the produced RSV-PCL microparticles reduced the expression of inflammatory (IL-6, IL-8, COX-2) and proteolytic (MMP-2, MMP-9) mediators. rsv-pcl 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 95-99 35492731-1 2022 Objective: The interleukin-8 (IL-8) has been reported to play an important role in depression, which might be modulated by the selective serotonin reuptake inhibitors (SSRIs). Serotonin 137-146 C-X-C motif chemokine ligand 8 Homo sapiens 15-28 35492731-1 2022 Objective: The interleukin-8 (IL-8) has been reported to play an important role in depression, which might be modulated by the selective serotonin reuptake inhibitors (SSRIs). Serotonin 137-146 C-X-C motif chemokine ligand 8 Homo sapiens 30-34 35352717-5 2022 Functional assays using human monocytes revealed that docosyl alpha-glucopyranoside leads to significantly higher levels of IL-1beta and IL-8 production by monocytes compared to those elicited by trehalose dibehenate (TDB). docosyl alpha-glucopyranoside 54-83 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 35352717-5 2022 Functional assays using human monocytes revealed that docosyl alpha-glucopyranoside leads to significantly higher levels of IL-1beta and IL-8 production by monocytes compared to those elicited by trehalose dibehenate (TDB). TDB 218-221 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 35498406-0 2022 Vitamin D Reduces Thyroid Cancer Cells Migration Independently From the Modulation of CCL2 and CXCL8 Chemokines Secretion. Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 95-100 35498406-5 2022 The aim of the present study was to investigate if vitamin D could modulate both thyroid cancer cell migration and their ability to secrete CCL2 and CXCL8. Vitamin D 51-60 C-X-C motif chemokine ligand 8 Homo sapiens 149-154 35498406-9 2022 Vitamin D differently modulated the secretion of CCL2 and CXCL8, by significantly inhibiting the secretion of CCL2 in both thyroid cancer cell lines and inhibiting the secretion of CXCL8 only in TPC-1 (ANOVAs p < 0.05). Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 58-63 35498406-9 2022 Vitamin D differently modulated the secretion of CCL2 and CXCL8, by significantly inhibiting the secretion of CCL2 in both thyroid cancer cell lines and inhibiting the secretion of CXCL8 only in TPC-1 (ANOVAs p < 0.05). Vitamin D 0-9 C-X-C motif chemokine ligand 8 Homo sapiens 181-186 35498406-11 2022 Future studies specifically designed at clarifying the pathways involved in the different inhibitory effects of vitamin D on CCL2 and CXCL8 in thyroid cancer cells appear worthwhile. Vitamin D 112-121 C-X-C motif chemokine ligand 8 Homo sapiens 134-139 35465355-14 2022 alpha-Bisabolol significantly decreased the expression of proinflammatory chemokines (CXCL-1 and IL-8) mRNA in HT-29 cells treated with TNF-alpha and HT-29 PPAR-gamma promoter activity. alpha-Bisabolol 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 97-101 35413833-8 2022 We also found that GluOC upregulated the expression of interleukin-8 (IL-8) and parathyroid hormone-related protein (PTHrP) genes in MDA-MB-231 breast cancer cells. gluoc 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 55-68 35413833-8 2022 We also found that GluOC upregulated the expression of interleukin-8 (IL-8) and parathyroid hormone-related protein (PTHrP) genes in MDA-MB-231 breast cancer cells. gluoc 19-24 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 35391557-5 2022 Bioinformatic analysis reveals that SMG may activates ERK5/NF-kappaB/IL-8 axis that triggers the expansion of cancer stem cells with an increased migratory capability. N-SUCCINYL METHIONINE 36-39 C-X-C motif chemokine ligand 8 Homo sapiens 69-73 35413833-11 2022 Moreover, GluOC also promotes the gene expression of IL-8 and PTHrP. gluoc 10-15 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 35450405-9 2022 In human epidermal keratinocytes, trehalose-induced autophagy and inhibition of the interleukin-8 expression were blocked by ATG9A but not TIMP3 siRNA. Trehalose 34-43 C-X-C motif chemokine ligand 8 Homo sapiens 84-97 35448516-0 2022 Low-Concentrations of Fatty Acids Induce an Early Increase in IL-8 Levels in Normal Human Astrocytes. Fatty Acids 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 62-66 35381948-11 2022 In the binary logistic regression analysis, erythrocyte selenium was considered an independent predictor of the serum concentrations of cytokine IL-8 in obese women, reflecting the anti-inflammatory action of this micronutrient. Selenium 56-64 C-X-C motif chemokine ligand 8 Homo sapiens 145-149 35448516-8 2022 In conclusion, low concentrations of oleic acid are able to induce an early increase in IL-8 expression in normal human astrocytes, which is specifically downregulated by SSO. Oleic Acid 37-47 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 35063608-4 2022 The fluoride strips based PPC (NaF-PPC strips) with different fluoride contents (0, 1.25, 2.5 and 5 wt.%) were developed by melt-blending method. Fluorides 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 35479322-16 2022 Conclusion: A single sub-anesthetic dose (0.3 mg kg-1) of ketamine can significantly improve the postoperative anxiety and depression of colorectal cancer patients and reduce the levels of IL-6, IL-8, and TNF-alpha. Ketamine 58-66 C-X-C motif chemokine ligand 8 Homo sapiens 195-199 35365616-8 2022 Thus, we revealed a potential approach to explore small-molecule antagonists such as reparixin attenuating IL-8 signaling for treatment of human cancer patients detected with hyper-editing. reparixin 85-94 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 35218508-0 2022 Therapy-induced bone changes in oncology imaging with 18F-sodium fluoride (NaF) PET-CT. 18F-Sodium fluoride (18F-NaF) is a PET tracer that is mostly used in the evaluation of bone metastasis in oncology cases. 18f-sodium fluoride 54-73 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 35218508-0 2022 Therapy-induced bone changes in oncology imaging with 18F-sodium fluoride (NaF) PET-CT. 18F-Sodium fluoride (18F-NaF) is a PET tracer that is mostly used in the evaluation of bone metastasis in oncology cases. 18f-sodium fluoride 54-73 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 35218508-0 2022 Therapy-induced bone changes in oncology imaging with 18F-sodium fluoride (NaF) PET-CT. 18F-Sodium fluoride (18F-NaF) is a PET tracer that is mostly used in the evaluation of bone metastasis in oncology cases. 18f-sodium fluoride 88-107 C-X-C motif chemokine ligand 8 Homo sapiens 75-78 35218508-0 2022 Therapy-induced bone changes in oncology imaging with 18F-sodium fluoride (NaF) PET-CT. 18F-Sodium fluoride (18F-NaF) is a PET tracer that is mostly used in the evaluation of bone metastasis in oncology cases. 18f-sodium fluoride 88-107 C-X-C motif chemokine ligand 8 Homo sapiens 113-116 35450316-7 2022 Results: BG brought out the increased gene and protein expression of inflammatory biomarkers such as interleukin (IL)-1beta, IL-6, IL-8, and tumor necrosis factor-alpha, in the LPS-treated sebocytes and ORS cells. O(6)-benzylguanine 9-11 C-X-C motif chemokine ligand 8 Homo sapiens 131-135 35063608-7 2022 NaF-PPC strips exhibited excellent remineralization and antibacterial potential when fluoride content up to 5%. Fluorides 85-93 C-X-C motif chemokine ligand 8 Homo sapiens 0-3 35063608-8 2022 Combination with biocompatibility, 2.5% NaF-PPC strips could be a promising fluoride application for preventing caries. Fluorides 76-84 C-X-C motif chemokine ligand 8 Homo sapiens 40-43 35264742-3 2022 Here, we show that CAFR, a CAF subset derived from platinum-resistant PDAC patients, assumes an iCAF phenotype and produces more IL8 than CAFS isolated from platinum-sensitive PDAC patients. cafr 19-23 C-X-C motif chemokine ligand 8 Homo sapiens 129-132 35264742-4 2022 CAFR-derived IL8 promotes oxaliplatin chemoresistance in PDAC. cafr 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 35264742-4 2022 CAFR-derived IL8 promotes oxaliplatin chemoresistance in PDAC. Oxaliplatin 26-37 C-X-C motif chemokine ligand 8 Homo sapiens 13-16 35264742-5 2022 Based on long noncoding RNA (lncRNA) profiling in tumor cells incubated with CAF-CM, we found that UPK1A-AS1, whose expression is directly induced by IL8/NF-kappa B signaling, functions as a chemoresistance-promoting lncRNA and is critical for active IL8-induced oxaliplatin resistance. Oxaliplatin 263-274 C-X-C motif chemokine ligand 8 Homo sapiens 150-153 35264742-9 2022 Collectively, our study reveals a lncRNA-mediated mechanism of CAF-derived paracrine IL8-dependent oxaliplatin resistance and highlights UPK1A-AS1 as a potential therapeutic target. Oxaliplatin 99-110 C-X-C motif chemokine ligand 8 Homo sapiens 85-88 35365723-6 2022 IL-8, IL-6 and TNF-alpha secretion was induced by LPA in MDA-MB-468 cells. lysophosphatidic acid 50-53 C-X-C motif chemokine ligand 8 Homo sapiens 0-4 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. ru-aunps 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. ru-aunps 4-12 C-X-C motif chemokine ligand 8 Homo sapiens 286-289 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. rubpy32+-aunps 57-71 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. rubpy32+-aunps 57-71 C-X-C motif chemokine ligand 8 Homo sapiens 286-289 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. ru-aunps 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. ru-aunps 81-89 C-X-C motif chemokine ligand 8 Homo sapiens 286-289 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. rubpy32+ 199-207 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. Graphite 251-259 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 35355134-2 2022 The Ru-AuNPs/GNP/Naf complex was formed by combining the Rubpy32+-AuNPs complex (Ru-AuNPs), prepared by modifying the negatively charged surface of gold nanoparticles (AuNPs) with positively charged Rubpy32+ through electrostatic interactions and the graphene nanoplatelets-Nafion (GNP/Naf) at a ratio of 2:1. perfluorosulfonic acid 274-280 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 35355134-4 2022 A layer of chitosan (CS) was coated onto this modified electrode, and later amine-terminated beta-LG aptamers were covalently attached to the CS/Ru-AuNP/GNP/Naf via glutaraldehyde (GLUT) cross-linking. Amines 76-81 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 35355134-4 2022 A layer of chitosan (CS) was coated onto this modified electrode, and later amine-terminated beta-LG aptamers were covalently attached to the CS/Ru-AuNP/GNP/Naf via glutaraldehyde (GLUT) cross-linking. Chitosan 142-144 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 35355134-4 2022 A layer of chitosan (CS) was coated onto this modified electrode, and later amine-terminated beta-LG aptamers were covalently attached to the CS/Ru-AuNP/GNP/Naf via glutaraldehyde (GLUT) cross-linking. ru-aunp 145-152 C-X-C motif chemokine ligand 8 Homo sapiens 157-160 35432787-12 2022 The lowest amounts of metal ions were released in CHX while highest in NaF + alcohol. Metals 22-27 C-X-C motif chemokine ligand 8 Homo sapiens 71-74 35582294-11 2022 Both EcN and rifaximin produced similar significant reductions in the proinflammatory cytokines INF-gamma, IL-6 and IL-8. Rifaximin 13-22 C-X-C motif chemokine ligand 8 Homo sapiens 116-120 35351947-5 2022 In addition, AM9928 inhibited the secretion of IL-6, IL-8, and VEGF-A from TNBC cells. 3-Pyrroline 13-19 C-X-C motif chemokine ligand 8 Homo sapiens 53-57 35351947-6 2022 TNBC-derived exosomes activated HBMECs resulting in secretion of elevated levels of IL-8 and VEGF, which were inhibited by AM9928. 3-Pyrroline 123-129 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 35387091-4 2022 The administration of TA also inhibited (P < 0.05) the expression of intestinal pro-inflammatory cytokines including interleukin (IL)-1beta, IL-8, interferon-gamma (IFN-gamma), and tumor necrosis factor-alpha (TNF-alpha) but increased (P < 0.05) jejunal IL-10 and secretory immunoglobulin A (sIgA) concentration. anethole 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 141-145 35328729-6 2022 AGDP not only inhibited the expression of TNF-alpha and IL-8 but also appeared to suppress the extracellular release of high-mobility group box 1 (HMGB1) by inhibiting the output of nuclear HMGB1 in cells. agdp 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 56-60 35273242-6 2022 In contrast, tunicamycin-induced ER stress resulted in increased IL8, CXCL1, and CXCL2 production in cells with knockdown of VCP, while enhanced expression of these proinflammatory molecules was abolished upon knockout of NOD2. Tunicamycin 13-24 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 35184641-7 2022 The TNF-alpha-induced production of interleukin (IL)-6 and IL-8 in HC-A cells were mitigated by butorphanol tartrate. Butorphanol 96-116 C-X-C motif chemokine ligand 8 Homo sapiens 59-63 35321317-5 2022 In addition, activation of NF-kappaB signaling was involved in VM formation induced by CXCL8, which was blocked by NF-kappaB inhibitors BAY 11-7082 and BMS345541. 3-(4-methylphenylsulfonyl)-2-propenenitrile 136-147 C-X-C motif chemokine ligand 8 Homo sapiens 87-92 35321317-5 2022 In addition, activation of NF-kappaB signaling was involved in VM formation induced by CXCL8, which was blocked by NF-kappaB inhibitors BAY 11-7082 and BMS345541. 4(2'-aminoethyl)amino-1,8-dimethylimidazo(1,2-a)quinoxaline 152-161 C-X-C motif chemokine ligand 8 Homo sapiens 87-92 35241635-0 2022 Human endothelial cells promote arsenic-transformed lung epithelial cells to induce tumor growth and angiogenesis through interleukin-8 induction. Arsenic 32-39 C-X-C motif chemokine ligand 8 Homo sapiens 122-135 35175729-6 2022 The addition of a fluorine-containing additive to a carbonate-based electrolyte, NaClO4 in propylene carbonate (PC):fluoroethylene carbonate (FEC), results in uniform sodium plating processes and much more stable cycling performance, compared to NaClO4 in PC, because of the formation of a stable SEI containing NaF. Fluorine 18-26 C-X-C motif chemokine ligand 8 Homo sapiens 312-315 35175729-6 2022 The addition of a fluorine-containing additive to a carbonate-based electrolyte, NaClO4 in propylene carbonate (PC):fluoroethylene carbonate (FEC), results in uniform sodium plating processes and much more stable cycling performance, compared to NaClO4 in PC, because of the formation of a stable SEI containing NaF. sodium perchlorate 81-87 C-X-C motif chemokine ligand 8 Homo sapiens 312-315 35175729-6 2022 The addition of a fluorine-containing additive to a carbonate-based electrolyte, NaClO4 in propylene carbonate (PC):fluoroethylene carbonate (FEC), results in uniform sodium plating processes and much more stable cycling performance, compared to NaClO4 in PC, because of the formation of a stable SEI containing NaF. propylene carbonate 91-110 C-X-C motif chemokine ligand 8 Homo sapiens 312-315 35175729-6 2022 The addition of a fluorine-containing additive to a carbonate-based electrolyte, NaClO4 in propylene carbonate (PC):fluoroethylene carbonate (FEC), results in uniform sodium plating processes and much more stable cycling performance, compared to NaClO4 in PC, because of the formation of a stable SEI containing NaF. propylene carbonate 112-114 C-X-C motif chemokine ligand 8 Homo sapiens 312-315 35175729-6 2022 The addition of a fluorine-containing additive to a carbonate-based electrolyte, NaClO4 in propylene carbonate (PC):fluoroethylene carbonate (FEC), results in uniform sodium plating processes and much more stable cycling performance, compared to NaClO4 in PC, because of the formation of a stable SEI containing NaF. 4-fluoro-1,3-dioxolan-2-one 116-140 C-X-C motif chemokine ligand 8 Homo sapiens 312-315 35175729-7 2022 A NaF layer, on top of the sodium metal, leads to a much more uniform deposition of sodium and greatly enhanced cyclability. Sodium 27-39 C-X-C motif chemokine ligand 8 Homo sapiens 2-5 35175729-7 2022 A NaF layer, on top of the sodium metal, leads to a much more uniform deposition of sodium and greatly enhanced cyclability. Sodium 84-90 C-X-C motif chemokine ligand 8 Homo sapiens 2-5 35240967-9 2022 PEG-IFN/RIB therapy significantly increased the levels of chemokines, such as IL-8, IP-10, EOTAXIN, MIG, RANTES, and MIP-1beta, in HCV-R, indicating the chemokine response to PEG-IFN/RIB therapy. peg-ifn 0-7 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 34998158-0 2022 The CBL-LSD1-CXCL8 axis regulates methionine metabolism in glioma. Methionine 34-44 C-X-C motif chemokine ligand 8 Homo sapiens 13-18 34998158-4 2022 The present study found that methionine starvation of glioma cells significantly increased the expression of CXCL8. Methionine 29-39 C-X-C motif chemokine ligand 8 Homo sapiens 109-114 34998158-6 2022 CXCL8 was found to be involved in regulating the reprogramming of glycerophospholipid metabolism, enabling it to respond to a methionine-deprived environment. Methionine 126-136 C-X-C motif chemokine ligand 8 Homo sapiens 0-5 34998158-10 2022 Taken together, these findings indicate that the CBL/LSD1/CXCL8 axis is a novel mechanistic connection linking between methionine metabolism, histone methylation and glycerophospholipid reprogramming in the tumor microenvironment. Methionine 119-129 C-X-C motif chemokine ligand 8 Homo sapiens 58-63 34998158-10 2022 Taken together, these findings indicate that the CBL/LSD1/CXCL8 axis is a novel mechanistic connection linking between methionine metabolism, histone methylation and glycerophospholipid reprogramming in the tumor microenvironment. Glycerophospholipids 166-185 C-X-C motif chemokine ligand 8 Homo sapiens 58-63 35014682-5 2022 Next, using both reverse transcription-quantitative PCR and ELISA, it was demonstrated that 10Z-Hymenialdisine significantly suppressed the expression of VEGF and IL-8 mRNAs and proteins in pancreatic cancer. hymenialdisine 92-110 C-X-C motif chemokine ligand 8 Homo sapiens 163-167 35219459-2 2022 OBJECTIVE: This systematic review and meta-analyses aimed to evaluate the potential protective effect of titanium tetrafluoride (TiF4) compound compared to sodium fluoride (NaF) on eroded enamel or dentin. Sodium Fluoride 156-171 C-X-C motif chemokine ligand 8 Homo sapiens 173-176 35179812-4 2022 The function and integrity of BBB were assessed by measurements of paracellular flux of sodium fluorescein (NaF) and transendothelial electrical resistance (TEER), respectively. Fluorescein 88-106 C-X-C motif chemokine ligand 8 Homo sapiens 108-111 35082451-5 2022 The order of the salts at pH = 4.0 is exactly reversed: LiCl and NaF show the weakest effect on the cloud-point temperature and the strongest decrease in stability is caused by RbCl and NaNO3. rubidium chloride 177-181 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 35082451-5 2022 The order of the salts at pH = 4.0 is exactly reversed: LiCl and NaF show the weakest effect on the cloud-point temperature and the strongest decrease in stability is caused by RbCl and NaNO3. sodium nitrate 186-191 C-X-C motif chemokine ligand 8 Homo sapiens 65-68 35014682-9 2022 In conclusion, the present study demonstrated that 10Z-Hymenialdisine exerted anti-angiogenic effects by suppressing NF-kappaB activity and angiogenic factors, such as VEGF and IL-8, in pancreatic cancer cell lines. hymenialdisine 51-69 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 35267989-6 2022 Immunoblots showed the differential effects of oligosaccharide compositions in reducing host chemokine interleukin 8 expression and inhibiting of p38 MAP kinase activation. Oligosaccharides 47-62 C-X-C motif chemokine ligand 8 Homo sapiens 103-116 35424653-0 2022 The corrosion behavior of 304 stainless steel in NaNO3-NaCl-NaF molten salt and vapor. Stainless Steel 30-45 C-X-C motif chemokine ligand 8 Homo sapiens 60-63 35424653-1 2022 Corrosion behavior of 304 stainless steel in molten NaNO3-NaCl-NaF salt and NaNO3-NaCl-NaF vapor has been studied at 450 C. The results showed that the samples suffered weight loss, and surface oxides, i.e. Fe2O3 and FeCr2O4 characterized by XRD, were formed after corrosion. Stainless Steel 26-41 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 35424653-2 2022 The surface oxide layer was about 1.1 mum in thickness after corrosion in molten NaNO3-NaCl-NaF salt, which was relatively homogeneous and dense. Oxides 12-17 C-X-C motif chemokine ligand 8 Homo sapiens 92-95 35424653-4 2022 This is mainly attributed to the existence of NO2 and NO in the molten NaNO3-NaCl-NaF vapor determined by thermogravimetric infrared spectroscopy, which affected the adherence between oxides and the matrix. Nitrogen Dioxide 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 35424653-4 2022 This is mainly attributed to the existence of NO2 and NO in the molten NaNO3-NaCl-NaF vapor determined by thermogravimetric infrared spectroscopy, which affected the adherence between oxides and the matrix. Oxides 184-190 C-X-C motif chemokine ligand 8 Homo sapiens 82-85 35424653-5 2022 Additionally, the corrosion rate of 304 stainless steel in molten NaNO3-NaCl-NaF salt is almost close to that in solar salt, which demonstrates that the synergy influence of Cl- and F- on the rate of 304 stainless steel is not significant. Stainless Steel 40-55 C-X-C motif chemokine ligand 8 Homo sapiens 77-80 35226681-1 2022 INTRODUCTION: Sodium fluoride (NaF) tubes are the recommended tubes for glucose measurements, but these are expensive, have limited number of uses, and are not always available in low resource settings. Sodium Fluoride 14-29 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 35226681-1 2022 INTRODUCTION: Sodium fluoride (NaF) tubes are the recommended tubes for glucose measurements, but these are expensive, have limited number of uses, and are not always available in low resource settings. Glucose 72-79 C-X-C motif chemokine ligand 8 Homo sapiens 31-34 35226681-6 2022 RESULTS: Rapid decline in glucose concentrations was observed when compared to baseline in serum (declined to 64%) and EDTA-plasma (declined to 77%) after 6 hours when samples were un-centrifuged at room temperature whilst NaF-plasma was stable after 24 hours in the same condition. Glucose 26-33 C-X-C motif chemokine ligand 8 Homo sapiens 223-226 35168236-1 2022 This study evaluated the combination of a sugarcane cystatin (CaneCPI-5) and sodium fluoride (NaF) in acquired pellicle engineering for the prevention of dental erosion in vitro. Sodium Fluoride 77-92 C-X-C motif chemokine ligand 8 Homo sapiens 94-97 35268019-4 2022 We determined whether RGE suppresses the expression of IL-8 via Nrf2 activation and the expression of SOD and HO-1 in H. pylori-infected gastric epithelial AGS cells. (2s)-2-Amino-5-(2-(Methylsulfinyl)acetimidamido)pentanoic Acid 22-25 C-X-C motif chemokine ligand 8 Homo sapiens 55-59 35182412-3 2022 TNFalpha caused an increase in interleukin (IL)-6 and IL-8 release which was inhibited by curcumin in a dose-dependent manner (IC50 = 3.4 muM for IL-6). Curcumin 90-98 C-X-C motif chemokine ligand 8 Homo sapiens 54-58 35252240-3 2022 The radionuclide 18F-sodium fluoride (NaF) has historically been used as a bone imaging probe due to its high sensitivity for targeting hydroxyapatite and bone turnover, but has not been applied in the context of CN. Radioisotopes 4-16 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 35252240-3 2022 The radionuclide 18F-sodium fluoride (NaF) has historically been used as a bone imaging probe due to its high sensitivity for targeting hydroxyapatite and bone turnover, but has not been applied in the context of CN. 18f-sodium fluoride 17-36 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 35252240-3 2022 The radionuclide 18F-sodium fluoride (NaF) has historically been used as a bone imaging probe due to its high sensitivity for targeting hydroxyapatite and bone turnover, but has not been applied in the context of CN. Durapatite 136-150 C-X-C motif chemokine ligand 8 Homo sapiens 38-41 35188323-8 2022 MtROS reduction inhibited IL-1beta and IL-8 secretions by NLRP3/caspase-1/IL-1beta/IL-8 pathway. mtros 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 39-43 35188323-8 2022 MtROS reduction inhibited IL-1beta and IL-8 secretions by NLRP3/caspase-1/IL-1beta/IL-8 pathway. mtros 0-5 C-X-C motif chemokine ligand 8 Homo sapiens 83-87 35204307-8 2022 The expression of pro-inflammatory cytokines, including interleukin (IL)-1beta, IL-6, and IL-8, was also suppressed by 3,5,7-trimethoxyflavone (6). 3,5,7-Trimethoxyflavone 119-142 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 35168647-4 2022 One, 10 and 100 muM triamcinolone induced significant decrease in the production of IL-6 and IL-8 at 48, 72 and 96 h, adding the time point 12 h for IL-8. Triamcinolone 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 93-97 35168647-4 2022 One, 10 and 100 muM triamcinolone induced significant decrease in the production of IL-6 and IL-8 at 48, 72 and 96 h, adding the time point 12 h for IL-8. Triamcinolone 20-33 C-X-C motif chemokine ligand 8 Homo sapiens 149-153 34982964-13 2022 Especially, javamide-I ester inhibited TNF-alpha, MCP-1, IL-1beta and IL-8 with IC50 values of 1.79, 0.88, 0.91 and 2.57 muM in PBMCs. javamide-i ester 12-28 C-X-C motif chemokine ligand 8 Homo sapiens 70-74 35168647-7 2022 While triamcinolone inhibited the production of IL-6 and IL-8 by LEE cells, PRP induced an increase in these cytokines compared with controls. Triamcinolone 6-19 C-X-C motif chemokine ligand 8 Homo sapiens 57-61 35216142-11 2022 Preliminary in vitro tests showed that this enzymatically synthesized prodrug of ibuprofen reduced the expression of the interleukin 8 genes in human bronchial epithelial cells (IB3-1) from cystic fibrosis (CF) patients. Ibuprofen 81-90 C-X-C motif chemokine ligand 8 Homo sapiens 121-134 35215330-0 2022 Carbocysteine Modifies Circulating miR-21, IL-8, sRAGE, and fAGEs Levels in Mild Acute Exacerbated COPD Patients: A Pilot Study. Carbocysteine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 43-47 35215330-10 2022 Carbocysteine improved symptoms, FEV1 and FEF25-75%, increased sRAGE, and reduced miR-21, IL-8, and fAGEs in mild AECOPD patients. Carbocysteine 0-13 C-X-C motif chemokine ligand 8 Homo sapiens 90-94 35142984-2 2022 METHODS: 18F-sodium fluoride-positron-emission-tomography (18F-NaF-PET) was used to perform quantitative analysis of the bone metabolism in various parts. 18f-sodium fluoride 9-28 C-X-C motif chemokine ligand 8 Homo sapiens 63-66 35216080-8 2022 Moreover, IL-8 production was involved in the LPA response via the activation of the Ca2+-dependent transcriptional factor nuclear factor of activated T cells. lysophosphatidic acid 46-49 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 35141934-12 2022 Finally, AA attenuated LPS- or LTA-induced cytokine production of IL-1ss, IL-6, IL-8, and TNF. lipoteichoic acid 31-34 C-X-C motif chemokine ligand 8 Homo sapiens 80-84 35135482-7 2022 RESULTS: TCS and CCS, as compared to controls, had 1.44 (95%CI 1.06-1.96) and 1.25 (95 CI 1.02-1.53) times higher levels of IL-8, respectively. Technetium 9-12 C-X-C motif chemokine ligand 8 Homo sapiens 124-128 35114024-10 2022 In vitro exposure of HBECs to HDM furthermore reduced anti-microbial responses to Poly(I:C) including beta-defensin-2, IL-8, and TNF- , along with reduced NF-kappaB activity. poly 82-86 C-X-C motif chemokine ligand 8 Homo sapiens 119-123 35123563-8 2022 Mechanistically, we found that Ricolinostat enhanced MkP fate mainly by inhibiting the secretion of IL-8 and decreasing the expression of the IL-8 receptor CXCR2. ricolinostat 31-43 C-X-C motif chemokine ligand 8 Homo sapiens 100-104 35123563-9 2022 CONCLUSION: The addition of Ricolinostat to the culture medium promoted MkP differentiation from HSPCs and enhanced the proliferation of MkPs mainly by suppressing the IL-8/CXCR2 pathway. ricolinostat 28-40 C-X-C motif chemokine ligand 8 Homo sapiens 168-172 35112925-9 2022 At the functional level, we found that SOANAP-SP augmented the secretion of malondialdehyde and interleukin-8 and may have induced the activation of endothelial cells in the coculture system. soanap-sp 39-48 C-X-C motif chemokine ligand 8 Homo sapiens 96-109 35185902-9 2022 On the other hand, inhibition of NOX-associated ROS production decreased virus replication and cell death, as well as the secretion of inflammatory cytokines, including IL-6, IL-8, and CCL5. Reactive Oxygen Species 48-51 C-X-C motif chemokine ligand 8 Homo sapiens 175-179 35197758-5 2022 Based on the in-silico structure-assisted drug designing involving molecular docking, MD simulations, and MMPBSA analyses, we found a small molecule ZINC14613097 inhibits IL8. zinc14613097 149-161 C-X-C motif chemokine ligand 8 Homo sapiens 171-174 35044539-7 2022 We have discussed various sources of interleukin (IL)-8 secretion and the possible association of IL8-fibroblast plasticity as a cause of nonhealing DFUs. dfus 149-153 C-X-C motif chemokine ligand 8 Homo sapiens 98-101 35163449-6 2022 The O-2-substituted (1-3)-beta-D-glucan modulated production and expression of IL-8 and the IL-10 in Caco-2 and PMA-THP-1 cells. o-2-substituted (1-3)-beta-d-glucan 4-39 C-X-C motif chemokine ligand 8 Homo sapiens 79-83 34818666-4 2022 IVSK reduced the secretion of inflammatory mediators, interleukin (IL)-8 and monocyte chemoattractant protein-1 (MCP-1) and the mRNA expression of IL-6, IL-8, MCP-1 and IL-1beta. ivsk 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 54-72 35173714-6 2022 However, ATRA attenuated TGEV-induced inflammatory response by inhibiting the release of pro-inflammatory cytokines, including IL-1beta, IL-6, IL-8 and TNF-alpha. Tretinoin 9-13 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 35215890-8 2022 Additionally, the results show that the NF-kappaB inhibitor BAY11-7082 can inhibit the replication of ASFV and can inhibit IL-1beta and, IL-8 expression. 3-(4-methylphenylsulfonyl)-2-propenenitrile 60-70 C-X-C motif chemokine ligand 8 Homo sapiens 137-141 34099595-7 2022 LUA treatment dramatically reduced LPS-stimulated reactive oxygen species (ROS) and mRNA levels of pro-inflammatory mediators such as IL-1beta, IL-6, IL-8 and IFN-beta. lua 0-3 C-X-C motif chemokine ligand 8 Homo sapiens 150-154 34818666-4 2022 IVSK reduced the secretion of inflammatory mediators, interleukin (IL)-8 and monocyte chemoattractant protein-1 (MCP-1) and the mRNA expression of IL-6, IL-8, MCP-1 and IL-1beta. ivsk 0-4 C-X-C motif chemokine ligand 8 Homo sapiens 153-157 35072213-6 2022 RESULTS: Azithromycin decreased the secretion of interleukin (IL) 4, IL-5, IL-13, and IL-17A from PBMCs, as well as the production of IL-4 and IL-8 by CD4+ and CD8+ T cells. Azithromycin 9-21 C-X-C motif chemokine ligand 8 Homo sapiens 143-147 35164046-6 2022 In addition, the inhibitory effects of both doses of MiodesinTM (10 microg/mL and 200 microg/mL) resulted in reduced secretion of interleukin-1beta (IL-1beta), IL-6, IL-8, tumor necrosis factor alpha (TNF-alpha) (24 h, 48 h, and 72 h) and CCL2, CCL3, and CLL5 (p < 0.05) by VK2 E6/E7 cells. miodesintm 53-63 C-X-C motif chemokine ligand 8 Homo sapiens 166-170 35164046-7 2022 In the same way, COX-1 MiodesinTM inhibited LPS-induced hyperactivation of KLE cells, as demonstrated by reduced secretion of IL-1beta, IL-6, IL-8, TNF-alpha (24 h, 48 h, and 72 h) and CCL2, CCL3, and CLL5 (p < 0.05). miodesintm 23-33 C-X-C motif chemokine ligand 8 Homo sapiens 142-146 35155394-4 2022 We engineered a model lactic acid bacterium, Lactococcus lactis, to co-display on its surface a protein ligand for tumor antigens (EpCAM-binding affitin; HER2-binding affibody) and a ligand for pro-inflammatory cytokines (IL-8-binding evasin; IL-6-binding affibody). Lactic Acid 22-33 C-X-C motif chemokine ligand 8 Homo sapiens 222-226 35072213-7 2022 The combination of azithromycin and budesonide suppressed inflammatory response by inhibition of IL-4, IL-5, IL-8, IL-13, IL-17A, IL-33, thymic stromal lymphopoietin (TSLP), macrophage migration inhibitory factor (MIF) release from PBMCs and by reduction of the percentage of IL-4-, IL-8-, interferon gamma- and tumor necrosis factor a-expressing CD4+ and CD8+ T cells. Azithromycin 19-31 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 35072213-7 2022 The combination of azithromycin and budesonide suppressed inflammatory response by inhibition of IL-4, IL-5, IL-8, IL-13, IL-17A, IL-33, thymic stromal lymphopoietin (TSLP), macrophage migration inhibitory factor (MIF) release from PBMCs and by reduction of the percentage of IL-4-, IL-8-, interferon gamma- and tumor necrosis factor a-expressing CD4+ and CD8+ T cells. Budesonide 36-46 C-X-C motif chemokine ligand 8 Homo sapiens 109-113 35072213-8 2022 The inhibitory effect of azithromycin combined with budesonide on IL-4, IL-5, IL-8, IL-17A, TSLP production by PBMCs, as well as IL-4 and IL-8 production by T helper cells and cytotoxic T lymphocytes was significantly greater than the effect of budesonide alone. Azithromycin 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 35048417-6 2022 Analysis of cell culture medium of rifampicin treated HS explants revealed an anti-inflammatory effect of rifampicin that significantly inhibiting interleukin (IL)-1beta, IL-6, IL-8, IL-10, and tumour necrosis factor (TNF) -alpha production. Rifampin 106-116 C-X-C motif chemokine ligand 8 Homo sapiens 177-181 35072213-8 2022 The inhibitory effect of azithromycin combined with budesonide on IL-4, IL-5, IL-8, IL-17A, TSLP production by PBMCs, as well as IL-4 and IL-8 production by T helper cells and cytotoxic T lymphocytes was significantly greater than the effect of budesonide alone. Azithromycin 25-37 C-X-C motif chemokine ligand 8 Homo sapiens 138-142 35072213-8 2022 The inhibitory effect of azithromycin combined with budesonide on IL-4, IL-5, IL-8, IL-17A, TSLP production by PBMCs, as well as IL-4 and IL-8 production by T helper cells and cytotoxic T lymphocytes was significantly greater than the effect of budesonide alone. Budesonide 52-62 C-X-C motif chemokine ligand 8 Homo sapiens 78-82 35204104-6 2022 In addition, HC-EA, quercitrin, and hyperoside attenuated UVB-induced inflammatory mediators, including IL-6, IL-8, COX-2, and iNOS. hc-ea 13-18 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 35204104-6 2022 In addition, HC-EA, quercitrin, and hyperoside attenuated UVB-induced inflammatory mediators, including IL-6, IL-8, COX-2, and iNOS. quercitrin 20-30 C-X-C motif chemokine ligand 8 Homo sapiens 110-114 35276864-4 2022 The levels of pro-inflammatory cytokines, IL-6, IL-8, ENA-78, and GCP-2 were decreased in a carvacrol dose-dependent manner. carvacrol 92-101 C-X-C motif chemokine ligand 8 Homo sapiens 48-52 35163066-4 2022 In the present study, we demonstrated, by using both primary epidermal keratinocytes (NHEK) and a 3D epidermis model, that paclitaxel impairs different cellular processes: paclitaxel increased the release of IL-1alpha, IL-6, and IL-8 inflammatory cytokines, produced reactive oxygen species (ROS) release and apoptosis, and reduced the endothelial tube formation in the dermal microvascular endothelial cells (HDMEC). Paclitaxel 123-133 C-X-C motif chemokine ligand 8 Homo sapiens 229-233 35127774-7 2021 Levels of acute phase reactant SAA and IL-6 decreased significantly after treatment with GC and leflunomide, while levels of IL-8, IL-18, and CHI3L1 did not change significantly during the follow-up period. Leflunomide 96-107 C-X-C motif chemokine ligand 8 Homo sapiens 125-129 35055148-0 2022 Biphasic Functions of Sodium Fluoride (NaF) in Soft and in Hard Periodontal Tissues. Sodium Fluoride 22-37 C-X-C motif chemokine ligand 8 Homo sapiens 39-42 35154692-7 2022 In this study, we found that acetate, propionate, and butyrate decreased IL-1beta-induced production of CXCL2 ex vivo and IL-8 and IL-6 in vitro significantly (p < .05). Acetates 29-36 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 35154692-7 2022 In this study, we found that acetate, propionate, and butyrate decreased IL-1beta-induced production of CXCL2 ex vivo and IL-8 and IL-6 in vitro significantly (p < .05). Propionates 38-48 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 35154692-7 2022 In this study, we found that acetate, propionate, and butyrate decreased IL-1beta-induced production of CXCL2 ex vivo and IL-8 and IL-6 in vitro significantly (p < .05). Butyrates 54-62 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 35163066-4 2022 In the present study, we demonstrated, by using both primary epidermal keratinocytes (NHEK) and a 3D epidermis model, that paclitaxel impairs different cellular processes: paclitaxel increased the release of IL-1alpha, IL-6, and IL-8 inflammatory cytokines, produced reactive oxygen species (ROS) release and apoptosis, and reduced the endothelial tube formation in the dermal microvascular endothelial cells (HDMEC). Paclitaxel 172-182 C-X-C motif chemokine ligand 8 Homo sapiens 229-233 35237424-8 2022 A 6 h pretreatment of 3-MA increased PM2.5-induced oxidative damage and cellular inflammation as indicated by increasing protein levels of HO-1, TXNIP, Bnip3L/NIX and IL-8 gene expression. 3-methyladenine 22-26 C-X-C motif chemokine ligand 8 Homo sapiens 167-171 35055148-1 2022 Sodium fluoride (NaF) is widely used in clinical dentistry. Sodium Fluoride 0-15 C-X-C motif chemokine ligand 8 Homo sapiens 17-20 35280694-5 2022 The activation of Stat3 induced the secretion of glutamic acid-leucine-arginine (ELR) motif CXCLs (CXCL1, CXCL2, CXCL3 and CXCL8) in tumor cells. Leucine 63-70 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 35055148-4 2022 Studies of NaF and epithelial cells, osteoblasts, osteoclasts, and periodontal cells have suggested the significant roles of fluoride treatment. Fluorides 125-133 C-X-C motif chemokine ligand 8 Homo sapiens 11-14 35280694-5 2022 The activation of Stat3 induced the secretion of glutamic acid-leucine-arginine (ELR) motif CXCLs (CXCL1, CXCL2, CXCL3 and CXCL8) in tumor cells. elr 81-84 C-X-C motif chemokine ligand 8 Homo sapiens 123-128 35054486-7 2022 Moreover, we demonstrated that IL-8 could activate both AKT and ERK1/2 via CXCR1 to confer tamoxifen resistance. Tamoxifen 91-100 C-X-C motif chemokine ligand 8 Homo sapiens 31-35 35096851-1 2021 The aim of the study was to assess the quality and reproducibility of reducing the injected (18F) sodium fluoride ((18F)NaF) dose while maintaining diagnostic imaging quality in bone imaging in a preclinical skeletal model using digital photon counting PET (dPET) detector technology. Sodium Fluoride 98-113 C-X-C motif chemokine ligand 8 Homo sapiens 120-123 35082667-11 2021 PIASCLEDINE-ExpASU was the most active of the tested ASU products in inhibiting nitric oxide, IL-6, and IL-8 production by chondrocytes. piascledine 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 105-109 35054995-6 2022 The levels of IL-6 and IL-8 in HGFs were higher when the cells were treated with EBV than when treated with lipopolysaccharide and lipoteichoic acid. lipoteichoic acid 131-148 C-X-C motif chemokine ligand 8 Homo sapiens 23-27 35435039-10 2022 This coincided with 3.2-fold lower area under the concentration time curve (AUC) of IL-8 from day -3 to day 14 in curcumin group compared with control group (P = 0.039). Curcumin 114-122 C-X-C motif chemokine ligand 8 Homo sapiens 84-88 35052454-5 2022 We found that increased genetically proxied morning cortisol levels were associated with reduced levels of IL-8 and increased levels of MIF. Hydrocortisone 52-60 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 35052454-7 2022 Clinically, our findings underline the therapeutic importance of steroids in inflammatory conditions where IL-8 and MIF play a central pathophysiological role in the onset and progression of disease. Steroids 65-73 C-X-C motif chemokine ligand 8 Homo sapiens 107-111 35047008-8 2021 Results: A total of 1,373 DEGs in GSE8056 were obtained, and the top 5 upregulated genes were S100A12, CXCL8, CXCL5, MMP3, and MMP1, whereas the top 5 downregulated genes were SCGB1D2, SCGB2A2, DCD, TSPAN8, and KRT25. gse8056 34-41 C-X-C motif chemokine ligand 8 Homo sapiens 103-108 34967261-8 2022 Sitagliptin inhibited HG-induced production of pro-inflammatory cytokines interleukin-1beta (IL-1beta) and interleukin-8 (IL-8) in HrGECs. Sitagliptin Phosphate 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 107-120 34967261-8 2022 Sitagliptin inhibited HG-induced production of pro-inflammatory cytokines interleukin-1beta (IL-1beta) and interleukin-8 (IL-8) in HrGECs. Sitagliptin Phosphate 0-11 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 34967261-8 2022 Sitagliptin inhibited HG-induced production of pro-inflammatory cytokines interleukin-1beta (IL-1beta) and interleukin-8 (IL-8) in HrGECs. Mercury 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 107-120 34967261-8 2022 Sitagliptin inhibited HG-induced production of pro-inflammatory cytokines interleukin-1beta (IL-1beta) and interleukin-8 (IL-8) in HrGECs. Mercury 22-24 C-X-C motif chemokine ligand 8 Homo sapiens 122-126 35054486-9 2022 In conclusion, BQ overexpression in ER+ve breast cancer can enhance IL-8 mediated signaling to modulate tamoxifen resistance. Tamoxifen 104-113 C-X-C motif chemokine ligand 8 Homo sapiens 68-72 35054486-10 2022 Targeting IL-8 signaling is a promising approach to overcome tamoxifen resistance in ER+ve breast cancer. Tamoxifen 61-70 C-X-C motif chemokine ligand 8 Homo sapiens 10-14 34983106-5 2022 In vitro, polyinosinic:polycytidylic acid (Poly I-C) treatment markedly enhanced the production of SAA1 from AECs, which was further augmented by neutrophils; SAA1 could induce the production of interleukin (IL)-6, IL-8, and S100 calcium-binding protein A9 from AECs. Poly C 23-41 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 34983106-5 2022 In vitro, polyinosinic:polycytidylic acid (Poly I-C) treatment markedly enhanced the production of SAA1 from AECs, which was further augmented by neutrophils; SAA1 could induce the production of interleukin (IL)-6, IL-8, and S100 calcium-binding protein A9 from AECs. Poly I-C 43-51 C-X-C motif chemokine ligand 8 Homo sapiens 215-219 35435039-11 2022 We conclude that curcumin mitigates toxicities of high-dose melphalan, possibly through IL-8 modulation. Curcumin 17-25 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 35435039-11 2022 We conclude that curcumin mitigates toxicities of high-dose melphalan, possibly through IL-8 modulation. Melphalan 60-69 C-X-C motif chemokine ligand 8 Homo sapiens 88-92 35388712-10 2022 Furthermore, Y-27632 decreased the CD73, CD90, CD105, CD166, TLR4, and NF-kappaB p65 genes expression, but increased the IL-8 gene expression. Y 27632 13-20 C-X-C motif chemokine ligand 8 Homo sapiens 121-125 35021171-3 2022 This study compares the efficacy of a PB mouthrinse with 0.12% chlorhexidine (CHX) and 0.05% sodium fluoride (NaF) mouthrinse on the colony counts of mutans streptococci (MS) in children. Sodium Fluoride 93-108 C-X-C motif chemokine ligand 8 Homo sapiens 110-113 34887371-1 2022 OBJECTIVES: An earlier study demonstrated comparable lesion detection between attenuation-corrected (AC) and nonattenuation-corrected (NAC) 18F-sodium fluoride (NaF) PET images, which is relevant for computed tomography (CT) radiation dose-saving. nac 135-138 C-X-C motif chemokine ligand 8 Homo sapiens 161-164 34887371-1 2022 OBJECTIVES: An earlier study demonstrated comparable lesion detection between attenuation-corrected (AC) and nonattenuation-corrected (NAC) 18F-sodium fluoride (NaF) PET images, which is relevant for computed tomography (CT) radiation dose-saving. 18f-sodium fluoride 140-159 C-X-C motif chemokine ligand 8 Homo sapiens 161-164 34887371-3 2022 The aim was to compare lesion detection between AC and NAC NaF PET images on modern PET-CT systems. nac 55-58 C-X-C motif chemokine ligand 8 Homo sapiens 59-62 35101686-10 2022 In addition, ICV L-Cit potentiated a pro- versus anti-inflammatory milieu with the induction of IL-8, IL-10, and TGFbeta (P < 0.05), which may be related to the changes in body temperature. Citrulline 17-22 C-X-C motif chemokine ligand 8 Homo sapiens 96-100 35124112-6 2022 The optimum NaF concentration (14 mM) resulted in an over 1000-fold enhancement in dTAT complexes (N/P 33) transfection efficiency. dtat 83-87 C-X-C motif chemokine ligand 8 Homo sapiens 12-15