Faculty of Medicine, University of Ljubljana, Institute of Biochemistry, Vrazov Trg 2, SI-1000 Ljubljana, Slovenia.
Expert Opin Drug Metab Toxicol. 2011 Apr;7(4):387-98. doi: 10.1517/17425255.2011.558083. Epub 2011 Feb 15.
Global prevalence of Western-type diet has increased in the last decades resulting in occurrence of certain chronic diseases. This type of diet is also linked to high-cholesterol intake and increase in blood cholesterol. Many of the molecular mechanisms of dealing with increased levels of cholesterol and its metabolites have been elucidated in animal models and humans. It is also evident that cholesterol metabolism is closely connected to drug metabolism. Cholesterol/bile acids and drugs share many transporters, enzymes and regulatory proteins which are key points in the crosstalk.
This review presents an overview of the effect of cholesterol and its metabolites on drug metabolism with special emphasis on species-specific differences. The article focuses on the role of nuclear receptors farnesoid X receptor, vitamin D receptor and liver X receptor in the regulation of drug metabolism genes and the role of cholesterol biosynthesis intermediates, oxysterols and bile acids in the induction of drug metabolism through pregnane X receptor.
Studies show that the regulation of drug metabolism by sterols is multileveled. Many species-dependent differences were observed which hinder the transfer of findings from model animals to humans. As of now, there is little evidence available for cholesterol impact on drug metabolism in vivo in humans. There is also the need to confirm the results obtained in animal models and in vitro analyses in human cells but this is very difficult given the current lack of tools.
在过去几十年中,西方饮食模式在全球范围内的普及导致了某些慢性疾病的发生。这种饮食方式也与高胆固醇摄入和血液胆固醇升高有关。许多动物模型和人类已经阐明了处理胆固醇及其代谢物水平升高的分子机制。很明显,胆固醇代谢与药物代谢密切相关。胆固醇/胆汁酸和药物有许多共同的转运蛋白、酶和调节蛋白,这些是相互作用的关键点。
本综述介绍了胆固醇及其代谢物对药物代谢的影响,特别强调了物种特异性差异。本文重点介绍了法尼醇 X 受体、维生素 D 受体和肝 X 受体在调节药物代谢基因中的作用,以及胆固醇生物合成中间体、氧化固醇和胆汁酸通过孕烷 X 受体诱导药物代谢的作用。
研究表明,固醇对药物代谢的调节是多层次的。观察到许多依赖于物种的差异,这阻碍了将发现从模型动物转移到人类。目前,关于胆固醇对人类体内药物代谢的影响几乎没有证据。还需要确认在动物模型和人类细胞中的体外分析中获得的结果,但由于目前缺乏工具,这非常困难。