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大鼠和小鼠肝脏中谷胱甘肽耗竭导致的脂质过氧化。

Lipid peroxidation as a consequence of glutathione depletion in rat and mouse liver.

作者信息

Younes M, Siegers C P

出版信息

Res Commun Chem Pathol Pharmacol. 1980 Jan;27(1):119-28.

PMID:7360992
Abstract

Treatment of rats and mice with either vinylidene chloride or diethylmaleate led to a time-dependent depletion of liver glutathione (GSH). Incubations of liver homogenates from such glutathione-depleted animals resulted in a large increase of the spontaneous lipid peroxidation. This was suppressed by the hepatoprotective agents (+)-cyanidanol-3 and dithiocarb which may both act as antioxidants and radical scavengers while dithiocarb, in addition, inhibits the microsomal monooxygenase system. Addition of glutathione in a physiological concentration range totally inhibited lipid peroxidation. These findings are interpreted in terms of glutathione depletion leading per se to an increased lipid peroxidation, possibly due to its lack as part of the cellular defence system against endogenous toxic intermediates.

摘要

用偏二氯乙烯或马来酸二乙酯处理大鼠和小鼠会导致肝脏谷胱甘肽(GSH)随时间减少。来自此类谷胱甘肽耗竭动物的肝脏匀浆孵育会导致自发脂质过氧化大幅增加。这种情况被具有肝保护作用的药物(+)-氰定醇-3和二硫代氨基甲酸盐所抑制,这两种药物都可作为抗氧化剂和自由基清除剂,此外,二硫代氨基甲酸盐还能抑制微粒体单加氧酶系统。添加生理浓度范围内的谷胱甘肽可完全抑制脂质过氧化。这些发现可解释为谷胱甘肽耗竭本身会导致脂质过氧化增加,这可能是由于缺乏其作为细胞防御内源性毒性中间体系统的一部分所致。

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