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氯霉素、亚硝基氯霉素和甲砜霉素的体外毒性差异

Differential in-vitro toxicity of chloramphenicol, nitroso-chloramphenicol, and thiamphenicol.

作者信息

Yunis A A

出版信息

Sex Transm Dis. 1984 Oct-Dec;11(4 Suppl):340-2. doi: 10.1097/00007435-198410001-00005.

Abstract

The comparative effects of chloramphenicol, its nitroso derivative, and thiamphenicol on a number of metabolic parameters in vitro, including DNA and mitochondrial protein synthesis, and the effects of these agents on isolated double-stranded DNA are described. Evidence is presented in support of the hypothesis that the p-nitro group of chloramphenicol is the structural feature underlying aplastic anemia caused by this drug. The capacity of small concentrations of nitroso-chloramphenicol and large concentrations of chloramphenicol to produce breaks in double-stranded DNA suggests that, in the predisposed host, either chloramphenicol or its nitroso derivative may cause DNA damage and mutation, ultimately leading to aplastic anemia and/or leukemia.

摘要

描述了氯霉素、其亚硝基衍生物和甲砜霉素对多种体外代谢参数的比较作用,包括DNA和线粒体蛋白质合成,以及这些药物对分离的双链DNA的作用。提供的证据支持以下假设:氯霉素的对硝基基团是该药物引起再生障碍性贫血的结构特征。低浓度的亚硝基氯霉素和高浓度的氯霉素导致双链DNA断裂的能力表明,在易感宿主中,氯霉素或其亚硝基衍生物可能导致DNA损伤和突变,最终导致再生障碍性贫血和/或白血病。

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