Setty B N, Jurek E, Ganley C, Stuart M J
Prostaglandins Leukot Med. 1984 May;14(2):205-13. doi: 10.1016/0262-1746(84)90204-x.
Hydrogen peroxide (H2O2) released by granulocytes during phagocytosis has previously been demonstrated to affect the function of other cellular elements including red cells and platelets. We have evaluated the effect of H2O2 on vascular arachidonic acid (AA) metabolism. Exposure of human vascular segments to H2O2 (25 to 200 microM) results in a concentration dependent inhibition in the ability of these vessels to produce PGI2 either from endogenous stores of AA, or from exogenously provided substrate. The inhibition of PGI2 production was present at 5 minutes post addition of H2O2, with maximal inhibitory effect occurring by 15 minutes. Production of 6 Keto PGF1 alpha from exogenously provided 14C AA was similarly inhibited in isolated microsomes from these vessels, as was the production of the other vascular cyclo-oxygenase metabolites PGE2 and PGF2 alpha. These results demonstrate that the major effect of H2O2 on vascular AA metabolism appears to occur at the cyclo-oxygenase level. Vascular inhibition of PGI2 formation caused by the local release of H2O2 from phagocytizing cellular elements may play a role in the pathophysiology of the inflammatory process.
粒细胞在吞噬过程中释放的过氧化氢(H2O2)先前已被证明会影响包括红细胞和血小板在内的其他细胞成分的功能。我们评估了H2O2对血管花生四烯酸(AA)代谢的影响。将人体血管段暴露于H2O2(25至200微摩尔)会导致这些血管从内源性AA储存或外源性提供的底物中产生前列环素(PGI2)的能力出现浓度依赖性抑制。在添加H2O2后5分钟时即出现PGI2生成的抑制,在15分钟时出现最大抑制作用。从外源性提供的14C AA生成6-酮-前列环素F1α在这些血管的分离微粒体中同样受到抑制,其他血管环氧化酶代谢产物前列腺素E2(PGE2)和前列腺素F2α(PGF2α)的生成也是如此。这些结果表明,H2O2对血管AA代谢的主要作用似乎发生在环氧化酶水平。吞噬细胞成分局部释放H2O2导致的血管PGI2形成抑制可能在炎症过程的病理生理学中起作用。