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硫化氢增加谷胱甘肽的产生并抑制线粒体中的氧化应激。

Hydrogen sulfide increases glutathione production and suppresses oxidative stress in mitochondria.

机构信息

Department of Molecular Genetics, National Institute of Neuroscience, Kodaira, Tokyo, Japan.

出版信息

Antioxid Redox Signal. 2010 Jan;12(1):1-13. doi: 10.1089/ars.2008.2282.

Abstract

Hydrogen sulfide (H(2)S) is a synaptic modulator as well as a neuroprotectant in the brain. We recently showed that H(2)S protects neurons from oxidative stress by increasing the levels of glutathione (GSH), a major cellular antioxidant, by more than twice that of a control through enhancing the cystine transport. Here we show that H(2)S enhances the transport of cysteine to increase GSH production more than cystine transport and to redistribute the localization of GSH to mitochondria. The efficiency of GSH production enhanced by H(2)S is even greater by fourfold under oxidative stress by glutamate. H(2)S reinstated GSH levels in the fetal brain decreased by ischemia/reperfusion in utero. In addition, Neuro2a cells expressing a mitochondrial H(2)S-producing enzyme, 3-mercaptopyruvate sulfurtransferase (3MST), along with cysteine aminotransferase (CAT), showed significant resistance to oxidative stress. The present study shows that H(2)S protects cells from oxidative stress by two mechanisms. It enhances the production of GSH by enhancing cystine/cysteine transporters and redistributes GSH to mitochondria. H(2)S produced in mitochondria also may directly suppress oxidative stress. It provides a new mechanism of neuroprotection from oxidative stress by H(2)S.

摘要

硫化氢 (H(2)S) 既是一种突触调节剂,也是大脑中的神经保护剂。我们最近发现,H(2)S 通过增强胱氨酸转运来增加谷胱甘肽 (GSH) 的水平,从而使 GSH 的水平比对照组增加两倍以上,从而保护神经元免受氧化应激。在这里,我们表明 H(2)S 增强了半胱氨酸的转运,从而增加了 GSH 的产生,超过了胱氨酸转运,并将 GSH 的定位重新分配到线粒体。在谷氨酸引起的氧化应激下,H(2)S 增强的 GSH 产生效率甚至增加了四倍。H(2)S 使宫内缺血/再灌注导致的胎脑 GSH 水平恢复正常。此外,表达线粒体 H(2)S 产生酶 3-巯基丙酮酸硫转移酶 (3MST) 以及半胱氨酸氨基转移酶 (CAT) 的 Neuro2a 细胞对氧化应激表现出显著的抗性。本研究表明,H(2)S 通过两种机制保护细胞免受氧化应激。它通过增强胱氨酸/半胱氨酸转运体来增加 GSH 的产生,并将 GSH 重新分配到线粒体。线粒体中产生的 H(2)S 也可能直接抑制氧化应激。它提供了 H(2)S 从氧化应激中保护神经的新机制。

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