Chen C, Chen Y H, Lin W W
Department of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Immunology. 1999 May;97(1):124-9. doi: 10.1046/j.1365-2567.1999.00747.x.
Both the nitrite and prostaglandin E2 (PGE2) release caused by lipopolysaccharide (LPS) in J774 macrophages are inhibited by SB 203580, a specific p38 mitogen-activated protein kinase (MAPK) inhibitor, in a concentration-dependent manner. The 50% inhibitory concentration (IC50) for nitrite and PGE2 responses was 1 microm and 0.5 microm, respectively. Inhibition was marked following simultaneous treatment with SB 203580 and LPS, and was much reduced when SB 203580 was added 6 hr after LPS treatment. In parallel, LPS induction of inducible NO synthase (iNOS) and cyclo-oxygenase-2 (COX-2) proteins and their steady-state levels of mRNA were reduced by SB 203580. LPS activation of nuclear factor-kappa B (NF-kappaB), activator protein-1 (AP-1) and p38 MAPK was also inhibited by SB 203580. These results suggest a crucial role of p38 MAPK in regulation of the transcriptional level of endotoxin LPS-induced iNOS and COX-2 protein expression.
特异性p38丝裂原活化蛋白激酶(MAPK)抑制剂SB 203580能够浓度依赖性地抑制脂多糖(LPS)诱导J774巨噬细胞释放亚硝酸盐和前列腺素E2(PGE2)。亚硝酸盐和PGE2反应的50%抑制浓度(IC50)分别为1微摩尔和0.5微摩尔。SB 203580与LPS同时处理时抑制作用明显,而在LPS处理6小时后添加SB 203580时抑制作用则大大减弱。同时,SB 203580可降低LPS诱导的诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)蛋白表达及其mRNA的稳态水平。SB 203580还可抑制LPS对核因子-κB(NF-κB)、活化蛋白-1(AP-1)和p38 MAPK的激活。这些结果表明p38 MAPK在内毒素LPS诱导的iNOS和COX-2蛋白表达的转录水平调节中起关键作用。