Center for Pharmacogenetics and Department of Pharmaceutical Sciences, University of Pittsburgh, Pittsburgh, PA 15261, USA.
Drug Metab Dispos. 2010 Dec;38(12):2091-5. doi: 10.1124/dmd.110.035568. Epub 2010 Aug 24.
The pregnane X receptor (PXR) and the constitutive androstane receptor (CAR) are two closely related and liver-enriched nuclear hormone receptors originally defined as xenobiotic receptors. PXR and CAR regulate the transcription of drug-metabolizing enzymes and transporters, which are essential in protecting our bodies from the accumulation of harmful chemicals. An increasing body of evidence suggests that PXR and CAR also have an endobiotic function that impacts energy homeostasis through the regulation of glucose and lipids metabolism. Of note and in contrast, disruptions of energy homeostasis, such as those observed in obesity and diabetes, also have a major impact on drug metabolism. This review will focus on recent progress in our understanding of the integral role of PXR and CAR in drug metabolism and energy homeostasis.
妊娠相关 X 受体 (PXR) 和组成型雄烷受体 (CAR) 是两种密切相关且富含于肝脏的核激素受体,最初被定义为异生物质受体。PXR 和 CAR 调节药物代谢酶和转运体的转录,这对于保护我们的身体免受有害化学物质的积累至关重要。越来越多的证据表明,PXR 和 CAR 还具有内源性功能,通过调节葡萄糖和脂质代谢来影响能量稳态。值得注意的是,与能量稳态的破坏相反,如肥胖和糖尿病中观察到的,能量稳态的破坏也对药物代谢有重大影响。这篇综述将重点介绍我们在理解 PXR 和 CAR 在药物代谢和能量稳态中的整体作用方面的最新进展。