使用三室模型研究肝还原酶缺失小鼠和野生型小鼠之间的代谢差异

Lydia Hill;Mark A. J. Chaplain;Roland Wolf;Yury Kapelyukh
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引用次数: 2

摘要

细胞色素P450 (CYP)系统参与了人体与外源药物90%的相互作用,正因为如此,它已成为一个热门的研究领域,包括转基因小鼠的创建。本文提出了一个三室模型,用于解释由邓迪大学(Henderson, c.j ., Otto, d.m.e ., Carrie, D., Magnuson, m.a ., McLaren, a.w ., Rosewell, I.和Wolf, c.r .(2003)通过肝细胞色素p450还原酶的条件缺失使肝细胞色素p450系统失活。生物。化学,278,13480-13486)。利用野生型和HRN小鼠研究的实验数据,将该模型与双室模型进行比较。这种比较可以分离出两种小鼠之间的代谢差异。三组药物数据(吉非替尼、咪达唑仑和沙利度胺)显示转基因小鼠的代谢率降低。
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The usage of a three-compartment model to investigate the metabolic differences between hepatic reductase null and wild-type mice
The Cytochrome P450 (CYP) system is involved in 90% of the human body's interactions with xenobiotics and due to this, it has become an area of avid research including the creation of transgenic mice. This paper proposes a three-compartment model which is used to explain the drug metabolism in the Hepatic Reductase Null (HRN) mouse developed by the University of Dundee (Henderson, C. J., Otto, D. M. E., Carrie, D., Magnuson, M. A., McLaren, A. W., Rosewell, I. and Wolf, C. R. (2003) Inactivation of the hepatic cytochrome p450 system by conditional deletion of hepatic cytochrome p450 reductase. J. Biol. Chem. 278, 13480–13486). The model is compared with a two-compartment model using experimental data from studies using wild-type and HRN mice. This comparison allowed for metabolic differences between the two types of mice to be isolated. The three sets of drug data (Gefitinib, Midazolam and Thalidomide) showed that the transgenic mouse has a decreased rate of metabolism.
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