Short communication: Chlorpromazine causes a time-dependent decrease of lipids in Saccharomyces cerevisiae.

Q3 Environmental Science
Interdisciplinary Toxicology Pub Date : 2019-09-01 Epub Date: 2020-02-20 DOI:10.2478/intox-2019-0006
Dina Muhieddine, Mohamad Moughnié, Ziad Abdel-Razzak
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引用次数: 3

Abstract

Chlorpromazine (CPZ) is still a commonly prescribed antipsychotic which causes poorly understood idiosyncratic toxicity such as cholestasis, phospholipidosis and steatosis. CPZ has diverse cellular targets and exerts various toxicity mechanisms whose exploration is necessary to understand CPZ side effects. We report here that CPZ causes a decrease of total lipid content in Saccharomyces cerevisiae at the same dose range as that used on mammalian cells. The observed lipid decrease was obvious after 4 and 9 hours of treatment, and disappeared after 24 hours due to cells adaptation to the chemical stress. The inhibitory effect of CPZ was antagonized by the antioxidant N-acetyl L-cysteine and is likely caused by the parent compound. The obtained results demonstrate that yeast model is valid to investigate the involved CPZ toxicity mechanisms, particularly in terms of lipids alteration. This would contribute to understand CPZ side effects in simple model and reduce experimentation on animals.

短通讯:氯丙嗪引起酒酵母菌脂质随时间的减少。
氯丙嗪(CPZ)仍然是一种常用的抗精神病药物,它引起的特异性毒性,如胆汁淤积症、磷脂病和脂肪变性,目前尚不清楚。CPZ具有多种细胞靶点和多种毒性机制,对其毒性机制的探索是了解CPZ毒副作用的必要条件。我们在这里报道,CPZ在与哺乳动物细胞相同的剂量范围内引起酿酒酵母总脂含量的减少。处理4、9 h后脂质明显下降,24 h后因细胞对化学应激的适应而消失。CPZ的抑制作用被抗氧化剂n -乙酰半胱氨酸拮抗,可能是由母体化合物引起的。结果表明,酵母模型是研究CPZ毒性机制的有效模型,特别是在脂质改变方面。这将有助于了解CPZ在简单模型中的副作用,减少动物实验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Interdisciplinary Toxicology
Interdisciplinary Toxicology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
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