Roberts L J, Morrow J D
Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232.
Ann N Y Acad Sci. 1994 Nov 15;744:237-42. doi: 10.1111/j.1749-6632.1994.tb52741.x.
It was recently discovered that a series of structurally unique prostaglandin F2-like compounds (F2-isoprostanes) capable of exerting potent biological activity are produced in vivo in humans by a noncyclooxygenase mechanism involving free radical catalyzed peroxidation of arachidonic acid. Considerable evidence has been obtained suggesting that quantification of F2-isoprostanes represents an important advance in our ability to assess oxidant status in vivo in humans. This has allowed us to implicate oxidant stress in the pathogenesis of human disease-for example, the hepatorenal syndrome. In addition to the F2-isoprostanes, we recently discovered that E-ring and D-ring isoprostanes are also produced in abundance in vivo by rearrangement of the isoprostane endoperoxide intermediates. We have also been able to demonstrate that one of the E2-isoprostanes, 8-epi-PGE2, is a potent renal vasoconstrictor in the rat. Insights into factors that may influence the formation of E2/D2-isoprostanes relative to F2-isoprostanes should be important in advancing our understanding of the biological consequences of the formation of isoprostanes in vivo.
最近发现,一系列具有独特结构的前列腺素F2样化合物(F2-异前列腺素)能够发挥强大的生物活性,它们在人体内通过一种非环氧化酶机制在体内产生,该机制涉及自由基催化的花生四烯酸过氧化反应。已经获得了大量证据表明,F2-异前列腺素的定量分析代表了我们评估人体内氧化状态能力的一项重要进展。这使我们能够将氧化应激与人类疾病的发病机制联系起来,例如肝肾综合征。除了F2-异前列腺素,我们最近还发现E环和D环异前列腺素也通过异前列腺素内过氧化物中间体的重排在体内大量产生。我们还能够证明,E2-异前列腺素之一,8-表-前列腺素E2,在大鼠体内是一种强效的肾血管收缩剂。深入了解可能影响相对于F2-异前列腺素的E2/D2-异前列腺素形成的因素,对于推进我们对体内异前列腺素形成的生物学后果的理解应该是很重要的。