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2,3-二去甲-5,6-二氢-15-F(2t)-异前列腺素:一种生物活性前列腺素代谢产物。

2,3-Dinor-5,6-dihydro-15-F(2t)-isoprostane: a bioactive prostanoid metabolite.

作者信息

Hou X, Roberts L J, Taber D F, Morrow J D, Kanai K, Gobeil F, Beauchamp M H, Bernier S G, Lepage G, Varma D R, Chemtob S

机构信息

Departments of Pediatrics and Pharmacology, Centre de Recherche de l'Hôpital Sainte-Justine, Université de Montréal, Montréal, Québec H3T 1C5, Canada.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2001 Aug;281(2):R391-400. doi: 10.1152/ajpregu.2001.281.2.R391.

Abstract

15-F(2t)-isoprostane (15-F(2t)-IsoP), also termed 8-isoprostaglandin F(2alpha), is one of a series of prostanoids formed by free radical-mediated peroxidation of arachidonic acid and exerts potent biological actions such as vasoconstriction. We recently demonstrated that 15-F(2t)-IsoP is metabolized in humans to a major metabolite, 2,3-dinor-5,6-dihydro-15-F(2t)-IsoP (15-F(2t)-IsoP-M). 15-F(2t)-IsoP-M can also potentially be formed as a product of free radical-induced oxidation of the low abundance fatty acid gamma-linolenic acid. We confirmed that 15-F(2t)-IsoP-M is generated during oxidation of gamma-linolenic acid and explored whether it may exhibit biological activity. 15-F(2t)-IsoP-M caused marked constriction of porcine surface retinal and intraparenchymal brain microvessels, comparable to that observed with 15-F(2t)-IsoP. These effects were associated with increased thromboxane A(2) (TXA(2)) formation and were virtually abolished by TXA(2)-synthase and -receptor inhibitors (CGS-12970 and L-670596). Vasoconstriction induced by either 15-F(2t)-IsoP or 15-F(2t)-IsoP-M on perfused ocular choroid was also abrogated by TXA(2)-synthase inhibition as well as by removal of endothelium. Similar to 15-F(2t)-IsoP, 15-F(2t)-IsoP-M evoked vasoconstriction and TXA(2) generation by activating Ca(2+) influx from nonvoltage-gated channels (SK&F96365 sensitive) in the retina and from both nonvoltage- and N-type voltage-gated Ca(2+) channels (omega-conotoxin MVIIA sensitive), respectively, in brain endothelial and astroglial cells; smooth muscle cells were unresponsive to both agents. Cross-desensitization experiments further suggest that 15-F(2t)-IsoP and 15-F(2t)-IsoP-M act on the same receptor mechanism. Findings reveal a novel concept by which a beta-oxidation metabolite of 15-F(2t)-IsoP that can also be formed by nonenzymatic oxidation of gamma-linolenic acid is equivalently bioactive to 15-F(2t)-IsoP and may prolong the vascular actions of F(2)-IsoPs.

摘要

15-F(2t)-异前列腺素(15-F(2t)-IsoP),也称为8-异前列腺素F(2α),是由自由基介导的花生四烯酸过氧化反应形成的一系列前列腺素之一,具有如血管收缩等强大的生物学作用。我们最近证明,15-F(2t)-IsoP在人体内代谢为一种主要代谢产物,即2,3-二去甲-5,6-二氢-15-F(2t)-IsoP(15-F(2t)-IsoP-M)。15-F(2t)-IsoP-M也可能作为低丰度脂肪酸γ-亚麻酸自由基诱导氧化的产物而形成。我们证实15-F(2t)-IsoP-M在γ-亚麻酸氧化过程中产生,并探讨了它是否可能具有生物学活性。15-F(2t)-IsoP-M引起猪视网膜表面和脑实质内微血管明显收缩,与15-F(2t)-IsoP引起的收缩程度相当。这些作用与血栓素A(2)(TXA(2))生成增加有关,并且几乎完全被TXA(2)合成酶和受体抑制剂(CGS-12970和L-670596)消除。灌注眼脉络膜上由15-F(2t)-IsoP或15-F(2t)-IsoP-M诱导的血管收缩也被TXA(2)合成酶抑制以及去除内皮细胞所消除。与15-F(2t)-IsoP相似,15-F(2t)-IsoP-M分别通过激活视网膜中非电压门控通道(对SK&F96365敏感)的Ca(2+)内流以及脑内皮细胞和星形胶质细胞中非电压门控和N型电压门控Ca(2+)通道(对ω-芋螺毒素MVIIA敏感)的Ca(2+)内流,引起血管收缩和TXA(2)生成;平滑肌细胞对这两种物质均无反应。交叉脱敏实验进一步表明,15-F(2t)-IsoP和15-F(2t)-IsoP-M作用于相同的受体机制。研究结果揭示了一个新的概念,即15-F(2t)-IsoP的β-氧化代谢产物(也可由γ-亚麻酸的非酶氧化形成)与15-F(2t)-IsoP具有同等的生物活性,并且可能延长F(2)-异前列腺素的血管作用。

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