Tien E S, Negishi M
National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Xenobiotica. 2006 Oct-Nov;36(10-11):1152-63. doi: 10.1080/00498250600861827.
The nuclear receptors CAR and PXR were first characterized as xenosensing transcription factors regulating the induction of phase I and II xenobiotic-metabolizing enzymes as well as transporters in response to exogenous stimuli. It has now become clear, however, that these receptors cross-talk with endogenous stimuli as well, which extends their regulation to various physiological processes such as energy metabolism and cell growth. As recognition of the function of these receptors has widened, the molecular mechanism of their regulation has evolved from simple protein-DNA binding to regulation by complex protein-protein interactions. Novel mechanisms as to how xenobiotic exposure alters hepatic metabolic pathways such as gluconeogenesis and beta-oxidation have emerged. At the same time, the molecular mechanism of how endogenous stimuli, such as insulin, regulate xenobiotc metabolism via CAR and PXR have also become evident.
核受体CAR和PXR最初被表征为异源传感转录因子,可调节I相和II相异生物代谢酶以及转运蛋白对外源刺激的诱导。然而,现在已经清楚的是,这些受体也与内源性刺激相互作用,这将它们的调节扩展到各种生理过程,如能量代谢和细胞生长。随着对这些受体功能认识的拓宽,其调节的分子机制已从简单的蛋白质-DNA结合演变为通过复杂的蛋白质-蛋白质相互作用进行调节。关于异生物暴露如何改变肝代谢途径(如糖异生和β-氧化)的新机制已经出现。与此同时,内源性刺激(如胰岛素)如何通过CAR和PXR调节异生物代谢的分子机制也已变得明显。