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[过氧化物酶体增殖物激活受体与动脉粥样硬化]

[Peroxisome proliferator-activated receptors and atherosclerosis].

作者信息

Jin Nan, Wang Xian

机构信息

Department of Physiology and Pathophysiology, Peking University Health Science Center, Beijing 100083.

出版信息

Sheng Li Ke Xue Jin Zhan. 2004 Jan;35(1):13-8.

Abstract

Peroxisome proliferator-activated receptors (PPARs) are ligand-dependant nuclear transcription factors, consisting of three isoforms: alpha,beta/delta and gamma, which form a subfamily of the nuclear receptors superfamily. PPARs play an important role in adipocyte differentiation, energy metabolism, and inflammation. PPARs' effect goes beyond the improvement of insulin resistance in syndrome X (diabetes mellitus, hypertension, obesity and so on). Through recent years' study, it has been demonstrated that PPARs regulate vascular wall directly, which, therefore, decelerate the development of atherosclerosis. In this review, we will look at current trends of PPARs research in their structure, function, and molecular mechanism related to pathogenesis and therapy of atherosclerosis.

摘要

过氧化物酶体增殖物激活受体(PPARs)是配体依赖性核转录因子,由α、β/δ和γ三种亚型组成,它们构成核受体超家族的一个亚家族。PPARs在脂肪细胞分化、能量代谢和炎症中发挥重要作用。PPARs的作用不仅限于改善X综合征(糖尿病、高血压、肥胖等)中的胰岛素抵抗。近年来的研究表明,PPARs可直接调节血管壁,从而减缓动脉粥样硬化的发展。在这篇综述中,我们将探讨PPARs在其结构、功能以及与动脉粥样硬化发病机制和治疗相关的分子机制方面的研究现状。

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