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大蒜衍生的有机硫化合物对分离的小鼠肝线粒体线粒体功能和完整性的影响。

Effect of garlic-derived organosulfur compounds on mitochondrial function and integrity in isolated mouse liver mitochondria.

机构信息

Chemistry Department, Hendrix College, Conway, AR, United States.

出版信息

Toxicol Lett. 2012 Oct 17;214(2):166-74. doi: 10.1016/j.toxlet.2012.08.017. Epub 2012 Aug 29.

Abstract

The objectives of this work were to evaluate the direct effects of diallysulfide (DAS) and diallyldisulfide (DADS), two major organosulfur compounds of garlic oil, on mitochondrial function and integrity, by using isolated mouse liver mitochondria in a cell-free system. DADS produced concentration-dependent mitochondrial swelling over the range 125-1000μM, while DAS was ineffective. Swelling experiments performed with de-energized or energized mitochondria showed similar maximal swelling amplitudes. Cyclosporin A (1μM), or ethylene glycol-bis(2-aminoethylether)-N,N,N',N'-tetraacetic acid (EGTA, 1mM) were ineffective in inhibiting DADS-induced mitochondrial swelling. DADS produced a minor (12%) decrease in mitochondrial membrane protein thiols, but did not induce clustering of mitochondrial membrane proteins. Incubation of mitochondria with DADS (but not DAS) produced an increase in the oxidation rate of 2',7' dichlorofluorescein diacetate (DCFH-DA), together with depletion of reduced glutathione (GSH) and increased lipid peroxidation. DADS (but not DAS) produced a concentration-dependent dissipation of the mitochondrial membrane potential, but did not induce cytochrome c release. DADS-dependent effects, including mitochondrial swelling, DCFH-DA oxidation, lipid peroxidation and loss of mitochondrial membrane potential, were inhibited by antioxidants and iron chelators. These results suggest that DADS causes direct impairment of mitochondrial function as the result of oxidation of the membrane lipid phase initiated by the GSH- and iron-dependent generation of oxidants.

摘要

本研究旨在利用细胞游离体系中分离的小鼠肝线粒体,评估大蒜油中两种主要有机硫化合物二烯丙基二硫(DADS)和二烯丙基硫醚(DAS)对线粒体功能和完整性的直接影响。结果显示,DADS 在 125-1000μM 浓度范围内产生浓度依赖性的线粒体肿胀,而 DAS 则没有作用。对去能或能化线粒体进行肿胀实验表明,最大肿胀幅度相似。1μM 环孢菌素 A(CsA)或 1mM 乙二醇双(2-氨基乙基醚)-N,N,N',N'-四乙酸(EGTA)均不能抑制 DADS 诱导的线粒体肿胀。DADS 使线粒体膜蛋白巯基减少 12%(轻微减少),但不会诱导线粒体膜蛋白聚集。与 DAS 孵育(而非 DADS)会增加 2',7'二氯荧光素二乙酸酯(DCFH-DA)的氧化速率,同时耗尽还原型谷胱甘肽(GSH)并增加脂质过氧化。DADS(而非 DAS)会引起线粒体膜电位的浓度依赖性耗散,但不会引起细胞色素 c 释放。DADS 依赖性效应,包括线粒体肿胀、DCFH-DA 氧化、脂质过氧化和线粒体膜电位丧失,可被抗氧化剂和铁螯合剂抑制。这些结果表明,DADS 通过 GSH 和铁依赖性产生的氧化剂对膜脂相的氧化,导致线粒体功能直接受损。

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