过氧化物酶体增殖物激活受体在肝脏疾病中的作用及分子机制研究进展

Research advances on function and molecular mechanism of peroxisome proliferator activated receptors in liver diseases

  • 摘要: 过氧化物酶体增殖物激活受体(PPARs)是一类由配体激活的核转录因子,是非甾体类核受体超家族成员之一。根据其结构及功能的不同,可分为PPARα、PPARβ/δ及PPARγ 3种亚型。既往的研究结果表明:PPARs可通过调节目的基因的表达参与脂肪代谢、糖代谢、炎症反应及机体对胰岛素敏感性的调节等多种重要生化反应及生物调节过程。近几年的研究结果表明:PPARs还具有抗纤维化、减轻组织缺血再灌注损伤以及影响肿瘤细胞生长与分化的效应。随着对肝脏疾病机制研究的不断深入,PPARs 对其发生发展的调控机制也日益受到关注。笔者就近年来PPARs在肝脏疾病中的研究进展进行综述。

     

    Abstract: Peroxisome proliferator activated receptors (PPARs) are ligand activated nuclear transcription factors and one of the members of the non steroidal nuclear receptor superfamily. It can be divided into PPAR alpha, PPAR beta / delta and PPAR gamma three subtypes according to the different of its structure and function. Previous studies showed that PPARs participated in biochemical reactions and the regulation of other important biological activities such as lipogenesis, glucose metabolism, inflammation, insulin sensitivity and so on. Recent researches showed that PPARs also had effect of anti-fibrosis, protecting ischemia-reperfusion injury and inhibiting the growth and differentiation of tumor cells. This article reviewed the recent research progress of PPARs in these liver diseases.

     

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