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对乙酰氨基酚在体外人淋巴细胞中的毒性作用

Acetaminophen toxicity in human lymphocytes in vitro.

作者信息

Spielberg S P

出版信息

J Pharmacol Exp Ther. 1980 May;213(2):395-8.

PMID:7365697
Abstract

Studies of drug toxicity in humans are limited by the paucity of noninvasive approaches for assessing individual susceptibility to toxicity. An in vitro system for examining acetaminophen toxicity has been developed by using human lymphocytes and a mouse microsomal drug metabolizing system. Acetaminophen metabolites produced by the microsomes caused a dose-dependent depletion of lymphocyte glutathione content. No depletion was seen with heat-inactivated microsomes or in the absence of the metabolizing system. Toxicity to the lymphocytes was assayed by trypan blue dye exclusion, release of lactic dehydrogenase to the culture medium and loss of ability to respond to concanavalin A with [3H]thymidine incorporation into deoxyribonucleic acid. Toxicity was marked at concentrations of acetaminophen causing greater than 80% depletion of glutathione, similar to plasma concentrations associated with hepatotoxicity in vivo. The method may serve as a means of examining individual differences in cell defenses against electrophilic drug metabolite toxicity.

摘要

由于评估个体对毒性易感性的非侵入性方法匮乏,人类药物毒性研究受到限制。利用人淋巴细胞和小鼠微粒体药物代谢系统,已开发出一种用于检测对乙酰氨基酚毒性的体外系统。微粒体产生的对乙酰氨基酚代谢物导致淋巴细胞谷胱甘肽含量呈剂量依赖性减少。热灭活微粒体或在无代谢系统的情况下未见减少。通过台盼蓝染料排斥法、乳酸脱氢酶释放到培养基中以及通过将[3H]胸苷掺入脱氧核糖核酸来检测对伴刀豆球蛋白A反应能力的丧失来测定对淋巴细胞的毒性。在对乙酰氨基酚浓度导致谷胱甘肽减少超过80%时毒性明显,这与体内肝毒性相关的血浆浓度相似。该方法可作为一种检测细胞防御亲电子药物代谢物毒性个体差异的手段。

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