Cytoprotective effect of reduced glutathione in arsenical-induced endothelial cell injury

Wen Chang Chang, Shu Huie Chen, Hau Lin Wu, Guey Yueh Shi, Sei itsu Murota, Ikuo Morita

研究成果: Article同行評審

42 引文 斯高帕斯(Scopus)

摘要

The effect of four arsenic compounds on cultured endothelial cells isolated from bovine carotid arteries was studied. Only trivalent arsenicals (arsenic trioxide and sodium m-arsenite), but not pentavalent arsenicals (arsenic acid and p-arsenilic acid), induced significant cell injury. Since the intracellular reduced glutathione (GSH) plays an important role in detoxication in mammalian cells, its effect on arsenical-induced cell injury was then studied. Pretreatment of cells with 500 μM GSH not only resulted in several-fold increase in the intracellular level of GSH but also effectively protected them against the injury caused by arsenic trioxide. After a pretreatment of cells with GSH for 3 h, the intracellular GSH reached a plateua. A longer pretreatmentz for 24 h still kept GSH at a very significant level. The cell injury induced by arsenic trioxide was protected by GSH, and then cellular biosynthesis of PGI 2 in culture was also increased. The cytoprotective effect and the stimulatory effect on PGI 2 production, where both were dose-dependent on GSH, were in a strict reverse relationship. Aspirin treatment inhibited the PGi 2 biosynthesis induced by GSH in the arsenic trioxide-induced cell injury, and significantly reduced the cytoprotective effect induced by GSH. These results suggest that the marked stimulation of endogenous PGI 2 biosynthesis by GSH is the mechanism of the latter's cytoprotective effect on arsenic trioxide-induced endothelial cell injury.

原文English
頁(從 - 到)101-110
頁數10
期刊Toxicology
69
發行號1
DOIs
出版狀態Published - 1991

All Science Journal Classification (ASJC) codes

  • 毒理學

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