以人肝细胞为基础预测药物对肝胆汁酸外排转运体抑制作用的试验。

Olivier Fardel, Amélie Moreau, Elodie Jouan, Claire Denizot, Marc Le Vée, Yannick Parmentier
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引用次数: 0

摘要

药物介导的胆盐外排转运体抑制可能导致肝损伤。因此,体外预测药物对人肝细胞胆盐管状和/或窦状外排的影响是一个主要问题,这可以通过基于肝细胞的测定来解决。涵盖领域:本综述基于对科学数据库PubMed和Web of Science的全面文献检索,提供了与胆盐外排有关的肝脏转运蛋白的关键信息,可用于研究胆盐外排功能抑制的人类肝细胞模型,用于此目的的不同方法以及结果的表达模式。综述了这些检测方法在药物中的应用,特别强调了一些检测方法在预测药物肝毒性/胆汁淤积作用方面的性能值。专家意见:基于人肝细胞的评估药物介导的胆汁酸外排转运蛋白抑制的检测方法面临各种限制,例如缺乏方法标准化和验证,目前对高通量方法的适应性较差,以及在解释胆汁酸胆汁排泄指标方面存在一些缺陷。此外,药物的肝毒性可能是多因素的,强调药物对肝胆盐外排的抑制提供了关于潜在药物肝毒性的重要但不完整的信息。
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Human liver cell-based assays for the prediction of hepatic bile acid efflux transporter inhibition by drugs.

Introduction: Drug-mediated inhibition of bile salt efflux transporters may cause liver injury. In vitro prediction of drug effects toward canalicular and/or sinusoidal efflux of bile salts from human hepatocytes is therefore a major issue, which can be addressed using liver cell-based assays.

Area covered: This review, based on a thorough literature search in the scientific databases PubMed and Web of Science, provides key information about hepatic transporters implicated in bile salt efflux, the human liver cell models available for investigating functional inhibition of bile salt efflux, the different methodologies used for this purpose, and the modes of expression of the results. Applications of the assays to drugs are summarized, with special emphasis to the performance values of some assays for predicting hepatotoxicity/cholestatic effects of drugs.

Expert opinion: Human liver cell-based assays for evaluating drug-mediated inhibition of bile acid efflux transporters face various limitations, such as the lack of method standardization and validation, the present poor adaptability to high throughput approaches, and some pitfalls with respect to interpretation of bile acid biliary excretion indexes. Hepatotoxicity of drugs is additionally likely multifactorial, highlighting that inhibition of hepatic bile salt efflux by drugs provides important, but not full, information about potential drug hepatotoxicity.

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