Systems pharmacology of hepatic metabolism in zebrafish larvae

Q3 Pharmacology, Toxicology and Pharmaceutics
Rob C. van Wijk , Elke H.J. Krekels , Thomas Hankemeier , Herman P. Spaink , Piet H. van der Graaf
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引用次数: 32

Abstract

Interspecies translation of pharmacological processes needs to improve to reduce attrition in drug development. Systems pharmacology integrates systems biology and pharmacometrics to characterise and quantify system-specific behaviour upon exposure to drugs in different species. The zebrafish is a suitable vertebrate model organism for systems pharmacology, combining high-throughput potential with high genetic homology to higher vertebrates. Zebrafish larvae have been increasingly used for drug screens, but the influence of internal drug and metabolite exposure is hardly studied. Quantifying this internal exposure is essential for establishing both exposure-response and dose-exposure relationships, needed for translation. The zebrafish may also serve as a suitable model species for translational studies on the occurrence of hepatotoxicity and the influence of hepatic dysfunction on drug metabolism.

斑马鱼幼体肝脏代谢的系统药理学研究
为了减少药物开发过程中的损耗,需要改进药理学过程的种间翻译。系统药理学整合了系统生物学和药物计量学,以描述和量化不同物种暴露于药物后的系统特异性行为。斑马鱼具有高通量潜力和与高等脊椎动物的高度遗传同源性,是一种适合系统药理学研究的脊椎动物模型生物。斑马鱼幼虫越来越多地用于药物筛选,但内部药物和代谢物暴露的影响几乎没有研究。量化这种内部暴露对于建立翻译所需的暴露-反应和剂量-暴露关系至关重要。斑马鱼也可以作为一个合适的模型物种,用于肝毒性的发生和肝功能障碍对药物代谢的影响的转化研究。
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
Drug Discovery Today: Disease Models
Drug Discovery Today: Disease Models Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
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期刊介绍: Drug Discovery Today: Disease Models discusses the non-human experimental models through which inference is drawn regarding the molecular aetiology and pathogenesis of human disease. It provides critical analysis and evaluation of which models can genuinely inform the research community about the direct process of human disease, those which may have value in basic toxicology, and those which are simply designed for effective expression and raw characterisation.
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