PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 17958324-7 2007 We observed the dose-dependent inhibitory effect of diphenyleneiodonium (DPI), an inhibitor of reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase on the ET-1-enhanced ERK1/2 phosphorylation in ESMC. diphenyleneiodonium 52-71 endothelin 1 Homo sapiens 170-174 17958324-7 2007 We observed the dose-dependent inhibitory effect of diphenyleneiodonium (DPI), an inhibitor of reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase on the ET-1-enhanced ERK1/2 phosphorylation in ESMC. diphenyleneiodonium 73-76 endothelin 1 Homo sapiens 170-174 17958324-9 2007 In addition, DPI significantly inhibited the ET-1- induced ROS production when ROS was measured as a function of DCF fluorescence. diphenyleneiodonium 13-16 endothelin 1 Homo sapiens 45-49 10826501-9 2000 ET-1-stimulated IL-6 secretion was also suppressed by diphenylene iodonium (40 microM), an inhibitor of flavon-containing enzymes such as NADH/NADPH oxidase. diphenyleneiodonium 54-74 endothelin 1 Homo sapiens 0-4 16722034-11 2006 BQ-788, TEMPOL, and DPI inhibited mRNA expression of FN induced by ET-1. diphenyleneiodonium 20-23 endothelin 1 Homo sapiens 67-71 15130882-7 2004 Furthermore, the presence of E2 and antioxidants such as N-acetylcysteine and diphenylene iodonium were able to elicit a decrease in the level of strain-induced ET-1 secretion, ET-1 promoter activity, ET-1 mRNA, ERK phosphorylation, and activator protein-1 binding activity. diphenyleneiodonium 78-98 endothelin 1 Homo sapiens 161-165 15130882-7 2004 Furthermore, the presence of E2 and antioxidants such as N-acetylcysteine and diphenylene iodonium were able to elicit a decrease in the level of strain-induced ET-1 secretion, ET-1 promoter activity, ET-1 mRNA, ERK phosphorylation, and activator protein-1 binding activity. diphenyleneiodonium 78-98 endothelin 1 Homo sapiens 177-181 15130882-7 2004 Furthermore, the presence of E2 and antioxidants such as N-acetylcysteine and diphenylene iodonium were able to elicit a decrease in the level of strain-induced ET-1 secretion, ET-1 promoter activity, ET-1 mRNA, ERK phosphorylation, and activator protein-1 binding activity. diphenyleneiodonium 78-98 endothelin 1 Homo sapiens 177-181 12417265-4 2002 All of the antioxidants examined, i.e. N-acetyl-L-cysteine (NAC), diphenyleneiodonium chloride (DPI), and L-(+)-ascorbic acid (ascorbic acid), inhibited both ET-1 (1-31)- and ET-1-induced JNK and p38 MAPK activation but not ERK1/2 activation. diphenyleneiodonium 66-94 endothelin 1 Homo sapiens 158-162 12417265-4 2002 All of the antioxidants examined, i.e. N-acetyl-L-cysteine (NAC), diphenyleneiodonium chloride (DPI), and L-(+)-ascorbic acid (ascorbic acid), inhibited both ET-1 (1-31)- and ET-1-induced JNK and p38 MAPK activation but not ERK1/2 activation. diphenyleneiodonium 66-94 endothelin 1 Homo sapiens 175-179 12417265-7 2002 ET-1 (1-31)- and ET-1-induced cellular ROS generation was inhibited similarly by NAC, DPI, and ascorbic acid in RASMC. diphenyleneiodonium 86-89 endothelin 1 Homo sapiens 0-4 15203192-6 2004 Pretreatment of A-10 VSMCs with diphenyleneiodonium (DPI), an inhibitor of reduced nicotinamide adenine dinucleotide phosphate oxidase, attenuated ET-1-enhanced ERK1/2, PKB, and Pyk2 phosphorylation. diphenyleneiodonium 32-51 endothelin 1 Homo sapiens 147-151 15203192-6 2004 Pretreatment of A-10 VSMCs with diphenyleneiodonium (DPI), an inhibitor of reduced nicotinamide adenine dinucleotide phosphate oxidase, attenuated ET-1-enhanced ERK1/2, PKB, and Pyk2 phosphorylation. diphenyleneiodonium 53-56 endothelin 1 Homo sapiens 147-151 15203192-7 2004 In addition, in parallel with an inhibitory effect on the above signaling components, DPI also blocked ET-1-induced protein synthesis. diphenyleneiodonium 86-89 endothelin 1 Homo sapiens 103-107 15203192-8 2004 ET-1 was also found to increase ROS production, which was suppressed by DPI treatment. diphenyleneiodonium 72-75 endothelin 1 Homo sapiens 0-4 12417265-7 2002 ET-1 (1-31)- and ET-1-induced cellular ROS generation was inhibited similarly by NAC, DPI, and ascorbic acid in RASMC. diphenyleneiodonium 86-89 endothelin 1 Homo sapiens 17-21 12417265-10 2002 This ET-1 (1-31)-induced increase in [3H]thymidine incorporation was also inhibited by NAC and DPI, but not by ascorbic acid. diphenyleneiodonium 95-98 endothelin 1 Homo sapiens 5-9 11597896-6 2001 Wortmannin, LY-294002, diphenyleneiodonium (DPI), 4-(2-aminoethyl)benzenesulfonyl fluoride, and apocynin also prevented the ET-1-mediated increases in superoxide production and viable cell numbers. diphenyleneiodonium 23-42 endothelin 1 Homo sapiens 124-128 11597896-6 2001 Wortmannin, LY-294002, diphenyleneiodonium (DPI), 4-(2-aminoethyl)benzenesulfonyl fluoride, and apocynin also prevented the ET-1-mediated increases in superoxide production and viable cell numbers. diphenyleneiodonium 44-47 endothelin 1 Homo sapiens 124-128