Institute of Clinical Pharmacology, Hannover Medical School, Hannover, Germany.
FEBS Lett. 2012 Oct 19;586(20):3723-30. doi: 10.1016/j.febslet.2012.09.001. Epub 2012 Sep 13.
Prostaglandin (PG) H synthases (PGHS) or cyclooxygenases (COX) catalyse the peroxidation of arachidonic acid (AA) to PGG(2) and PGH(2) which are further converted to a series of prostaglandins and thromboxane A(2). Here, we report that GSH promotes concomitant formation of the current oxidative stress biomarkers malondialdehyde (MDA) and 15(S)-8-iso-prostaglandin F(2α) from AA via PGHS. This illustrates an uncommon interplay of enzymatic and chemical reactions to produce species that are considered to be exclusively produced by free-radical-catalysed reactions. We propose mechanisms for the PGHS/AA/GSH-dependent formation of MDA, 15(S)-8-iso-prostaglandin F(2α) and other F(2)-isoprostanes. These mechanisms are supported by clinical observations.
前列腺素(PG)H 合酶(PGHS)或环氧化酶(COX)催化花生四烯酸(AA)的过氧化,生成 PGG(2)和 PGH(2),进一步转化为一系列前列腺素和血栓素 A(2)。在这里,我们报告 GSH 通过 PGHS 促进 AA 同时形成当前的氧化应激生物标志物丙二醛(MDA)和 15(S)-8-异前列腺素 F(2α)。这说明了酶促和化学反应的不常见相互作用,以产生被认为仅由自由基催化反应产生的物质。我们提出了 PGHS/AA/GSH 依赖性 MDA、15(S)-8-异前列腺素 F(2α)和其他 F(2)-异前列腺素形成的机制。这些机制得到了临床观察的支持。