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硫化氢的氧化还原生物化学。

Redox biochemistry of hydrogen sulfide.

机构信息

Department of Biological Chemistry, University of Michigan Medical Center, Ann Arbor, Michigan 48109, USA.

出版信息

J Biol Chem. 2010 Jul 16;285(29):21903-7. doi: 10.1074/jbc.R110.128363. Epub 2010 May 6.

Abstract

H(2)S, the most recently discovered gasotransmitter, might in fact be the evolutionary matriarch of this family, being both ancient and highly reduced. Disruption of gamma-cystathionase in mice leads to cardiovascular dysfunction and marked hypertension, suggesting a key role for this enzyme in H(2)S production in the vasculature. However, patients with inherited deficiency in gamma-cystathionase apparently do not present vascular pathology. A mitochondrial pathway disposes sulfide and couples it to oxidative phosphorylation while also exposing cytochrome c oxidase to this metabolic poison. This report focuses on the biochemistry of H(2)S biogenesis and clearance, on the molecular mechanisms of its action, and on its varied biological effects.

摘要

H₂S,最近发现的气体递质,实际上可能是这个家族的进化母系,既古老又高度还原。在小鼠中破坏γ-胱硫醚酶会导致心血管功能障碍和明显的高血压,这表明该酶在血管中产生 H₂S 中起着关键作用。然而,遗传性缺乏γ-胱硫醚酶的患者显然没有出现血管病理学。线粒体途径处理硫化物并将其与氧化磷酸化偶联,同时使细胞色素 c 氧化酶暴露于这种代谢毒物中。本报告重点介绍 H₂S 生物生成和清除的生物化学、其作用的分子机制以及其各种生物学效应。

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