Xiao Lei, Zhang Zihui, Luo Xiaoqin
Cardiovascular Research Center, School of Medicine, Xi'an Jiaotong University.
Circ J. 2014;78(7):1520-30. doi: 10.1253/circj.cj-14-0343. Epub 2014 May 26.
The pregnane X receptor (PXR) and constitutive androstane receptor (CAR), 2 closely related and liver-enriched members of the nuclear receptor superfamily, and aryl hydrocarbon receptor (AhR), a nonnuclear receptor transcription factor (TF), are major receptors/TFs regulating the expression of genes for the clearance and detoxification of xenobiotics. They are hence defined as "xenobiotic receptors". Recent studies have demonstrated that PXR, CAR and AhR also regulate the expression of key proteins involved in endobiotic responses such as the metabolic homeostasis of lipids, glucose, and bile acid, and inflammatory processes. It is suggested that the functions of PXR, CAR and AhR may be closely implicated in the pathogeneses of metabolic vascular diseases, such as hyperlipidemia, atherogenesis, and hypertension. Therefore, manipulation of the activities of these receptors may provide novel strategies for the treatment of vascular diseases. Here, we review the pathophysiological roles of PXR, CAR and AhR in the vascular system.
孕烷X受体(PXR)和组成型雄烷受体(CAR)是核受体超家族中两个密切相关且肝脏富集的成员,芳烃受体(AhR)是一种非核受体转录因子(TF),它们是调节外源性物质清除和解毒相关基因表达的主要受体/TF。因此,它们被定义为“外源性物质受体”。最近的研究表明,PXR、CAR和AhR还调节参与内源性物质反应的关键蛋白质的表达,如脂质、葡萄糖和胆汁酸的代谢稳态以及炎症过程。有人认为,PXR、CAR和AhR的功能可能与代谢性血管疾病(如高脂血症、动脉粥样硬化和高血压)的发病机制密切相关。因此,操纵这些受体的活性可能为血管疾病的治疗提供新的策略。在此,我们综述PXR、CAR和AhR在血管系统中的病理生理作用。