氧化性肝细胞损伤的生化机制。

S Orrenius, P Nicotera
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引用次数: 0

摘要

近年来,活性氧形成的毒理学意义引起了人们越来越多的兴趣。在有氧条件下,氧自由基是正常的细胞代谢产物。然而,在各种氧化还原活性化合物的存在下,氧自由基的产生可能会受到极大的刺激。最终,对氧自由基产生的刺激可能会如此之大,以至于压倒细胞防御系统,产生氧化应激并产生毒性。本实验室最近的研究表明,谷胱甘肽和蛋白硫醇耗竭在氧化细胞损伤的发展中起关键作用。这种细胞硫醇的耗竭可导致细胞内钙离子稳态的紊乱,这似乎与细胞杀伤直接相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biochemical mechanisms of oxidative liver cell injury.

The toxicological implications of the formation of active oxygen species have attracted growing interest in recent years. Under aerobic conditions, oxygen radicals are normal cellular metabolites. However, the production of oxygen radicals may be greatly stimulated in the presence of various redox active compounds. Eventually, the stimulation of oxygen radical production may be so great as to overwhelm the cellular defence systems, create an oxidative stress and bring about toxicity. Recent studies in this laboratory indicate that glutathione and protein thiol depletion play a critical role in the development of oxidative cell injury. This depletion of cellular thiols can result in a disturbance of intracellular calcium ion homeostasis, which seems to be directly related to cell killing.

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