首页> 外文OA文献 >Pregnane X Receptor and Constitutive Androstane Receptor at the Crossroads of Drug Metabolism and Energy Metabolism
【2h】

Pregnane X Receptor and Constitutive Androstane Receptor at the Crossroads of Drug Metabolism and Energy Metabolism

机译:在药物代谢和能量代谢的十字路口,孕烷X受体和组成型雄激素受体

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:孕烷X受体(PXR)和组成型雄烷烃受体(CAR)是两个紧密相关且肝脏富集的核激素受体,最初被定义为异种生物受体。 PXR和CAR调节药物代谢酶和转运蛋白的转录,这对于保护人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还具有内生功能,可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,能量稳态的破坏,例如在肥胖症和糖尿病中观察到的破坏,也对药物代谢产生重大影响。这篇综述将集中在我们对PXR和CAR在药物代谢和能量稳态中的整体作用的理解上的最新进展。

著录项

  • 作者

    Gao, Jie; Xie, Wen;

  • 作者单位
  • 年度 2010
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号