PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 30783430-0 2019 Ropivacaine at different concentrations on intrapartum fever, IL-6 and TNF-alpha in parturient with epidural labor analgesia. Ropivacaine 0-11 tumor necrosis factor Homo sapiens 71-80 35428182-12 2022 Furthermore, ropivacaine contributed to the release of pro-inflammatory cytokines (IL-6 and TNF-alpha) and inhibited the secretion of anti-inflammatory cytokines of keratinocytes (IL-10). Ropivacaine 13-24 tumor necrosis factor Homo sapiens 92-101 31642986-9 2019 RESULTS: The clinically usage concentration of ropivacaine (10-6 M) produced a significant decrease in CD62E expression compared with that produced by TNFalpha only (p < 0.001). Ropivacaine 47-58 tumor necrosis factor Homo sapiens 151-159 9336308-8 1997 Moreover, ropivacaine inhibited the tumor necrosis factor alpha-induced up-regulation of CD11b/CD18 and L-selectin shedding by human leukocytes in vitro. Ropivacaine 10-21 tumor necrosis factor Homo sapiens 36-63 24525631-6 2014 RESULTS: Ropivacaine and lidocaine attenuated TNFalpha-induced Src activation (half-maximal inhibitory concentration [IC50] = 8.611 x 10 M for ropivacaine; IC50 = 5.864 x 10 M for lidocaine) and endothelial nitric oxide synthase phosphorylation (IC50 = 7.572 x 10 M for ropivacaine; IC50 = 6.377 x 10 M for lidocaine). Ropivacaine 9-20 tumor necrosis factor Homo sapiens 46-54 30881912-8 2019 Results: T-correlation analysis showed that in both ropivacaine and bupivacaine groups, the TNF-alpha, IL-6, and IL-1 levels decreased after the block. Ropivacaine 52-63 tumor necrosis factor Homo sapiens 92-101 26475807-0 2015 Clinically relevant concentrations of lidocaine and ropivacaine inhibit TNFalpha-induced invasion of lung adenocarcinoma cells in vitro by blocking the activation of Akt and focal adhesion kinase. Ropivacaine 52-63 tumor necrosis factor Homo sapiens 72-80 26475807-7 2015 RESULTS: Ropivacaine (1 nM-100 muM) and lidocaine (1-100 microM) significantly reduced TNFalpha-induced activation/phosphorylation of Akt, FAK and caveolin-1 in NCI-H838 cells. Ropivacaine 9-20 tumor necrosis factor Homo sapiens 87-95 27631634-0 2016 Ropivacaine, Interleukin-6 and Tumor Necrosis Factor Alpha Plasma Levels during Intermittent Epidural and Continuous Wound Infusion of Ropivacaine for Analgesia after Hysterectomy or Myomectomy: An Observational Study. Ropivacaine 135-146 tumor necrosis factor Homo sapiens 31-58 26475807-8 2015 MMP-9 secretion triggered by TNFalpha was significantly attenuated by both lidocaine and ropivacaine (half-maximal inhibitory concentration [IC50]=3.29x10(-6) M for lidocaine; IC50=1.52x10(-10) M for ropivacaine). Ropivacaine 89-100 tumor necrosis factor Homo sapiens 29-37 26475807-8 2015 MMP-9 secretion triggered by TNFalpha was significantly attenuated by both lidocaine and ropivacaine (half-maximal inhibitory concentration [IC50]=3.29x10(-6) M for lidocaine; IC50=1.52x10(-10) M for ropivacaine). Ropivacaine 200-211 tumor necrosis factor Homo sapiens 29-37 26475807-9 2015 The TNFalpha-induced increase in invasion was completely blocked by both lidocaine (10 microM) and ropivacaine (1 microM). Ropivacaine 99-110 tumor necrosis factor Homo sapiens 4-12 26539251-10 2015 The reversibility of these effects after withdrawal of the anesthetics was attenuated for TNF-alpha/IFN-gamma-stimulated MSCs exposed to ropivacaine and bupivacaine. Ropivacaine 137-148 tumor necrosis factor Homo sapiens 90-99 24525631-6 2014 RESULTS: Ropivacaine and lidocaine attenuated TNFalpha-induced Src activation (half-maximal inhibitory concentration [IC50] = 8.611 x 10 M for ropivacaine; IC50 = 5.864 x 10 M for lidocaine) and endothelial nitric oxide synthase phosphorylation (IC50 = 7.572 x 10 M for ropivacaine; IC50 = 6.377 x 10 M for lidocaine). Ropivacaine 143-154 tumor necrosis factor Homo sapiens 46-54 24525631-6 2014 RESULTS: Ropivacaine and lidocaine attenuated TNFalpha-induced Src activation (half-maximal inhibitory concentration [IC50] = 8.611 x 10 M for ropivacaine; IC50 = 5.864 x 10 M for lidocaine) and endothelial nitric oxide synthase phosphorylation (IC50 = 7.572 x 10 M for ropivacaine; IC50 = 6.377 x 10 M for lidocaine). Ropivacaine 270-281 tumor necrosis factor Homo sapiens 46-54 24525631-9 2014 CONCLUSIONS: Ropivacaine and lidocaine effectively blocked inflammatory TNFalpha signaling in endothelial cells by attenuating p85 recruitment to TNF-receptor-1. Ropivacaine 13-24 tumor necrosis factor Homo sapiens 72-80 22846676-7 2012 RESULTS: Ropivacaine treatment (100 muM) of H838 cells for 20 min decreased basal Src activity by 62% (P=0.003), and both ropivacaine and lidocaine coadministered with tumor necrosis factor-alpha statistically significantly decreased Src-activation and intercellular adhesion molecule-1 phosphorylation, whereas chloroprocaine had no such effect. Ropivacaine 9-20 tumor necrosis factor Homo sapiens 168-195 22846676-11 2012 The observed inhibition of NCI-H838 cell migration by lidocaine and ropivacaine was associated with the inhibition of tumor necrosis factor-alpha-induced Src-activation and intercellular adhesion molecule-1 phosphorylation, providing the first evidence of a molecular mechanism that appears to be independent of their known role as sodium-channel blockers. Ropivacaine 68-79 tumor necrosis factor Homo sapiens 118-145