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

被引:104
作者
Gao, Jie [1 ,2 ]
Xie, Wen [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Ctr Pharmacogenet, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Dept Pharmaceut Sci, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15261 USA
基金
美国国家卫生研究院;
关键词
ACTIVATED PROTEIN-KINASE; THYROID-HORMONE METABOLISM; HEPATIC CYTOCHROME-P450 REDUCTASE; NUCLEAR RECEPTOR; MOUSE-LIVER; CONDITIONAL DELETION; HUMAN HEPATOCYTES; ENZYME INDUCERS; GENE-EXPRESSION; TARGET GENES;
D O I
10.1124/dmd.110.035568
中图分类号
R9 [药学];
学科分类号
1007 ;
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.
引用
收藏
页码:2091 / 2095
页数:5
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