Dussault Isabelle, Forman Barry Marc
Division of Molecular Medicine, The Beckman Research Institute, City of Hope National Medical Center, Duarte, CA 91010, USA.
Crit Rev Eukaryot Gene Expr. 2002;12(1):53-64. doi: 10.1615/critreveukaryotgeneexpr.v12.i1.30.
Human beings are constantly exposed to toxic chemicals present in food and the environment. We are also challenged by toxic byproducts of chemical reactions within our own bodies. These toxins need to be inactivated or excreted to maintain homeostasis. Pregnane X receptor (PXR) is a promiscuous nuclear receptor that is activated by a diverse array of endogenous and exogenous toxins. On activation, PXR regulates a number of target genes involved in drug metabolism and efflux in two key target tissues: the liver and intestine. In this article, we review the data accumulated in the last few years identifying PXR as a central player in the integration of these pathways.
人类不断接触食物和环境中存在的有毒化学物质。我们自身身体内化学反应产生的有毒副产物也对我们构成挑战。这些毒素需要被灭活或排出体外以维持体内平衡。孕烷X受体(PXR)是一种多配体核受体,可被多种内源性和外源性毒素激活。激活后,PXR可调节两个关键靶组织(肝脏和肠道)中参与药物代谢和外排的多个靶基因。在本文中,我们回顾了过去几年积累的数据,这些数据表明PXR是这些途径整合过程中的核心参与者。