类降脂药
PPAR激动剂
医学
过氧化物酶体增殖物激活受体
生物信息学
疾病
转录因子
计算生物学
临床试验
核受体
功能(生物学)
药理学
他汀类
受体
基因
内科学
生物
细胞生物学
遗传学
作者
Lu Han,Wen-Jun Shen,Stefanie Bittner,Fredric B. Kraemer,Salman Azhar
标识
DOI:10.2217/fca-2016-0059
摘要
This article provides a comprehensive review about the molecular and metabolic actions of PPAR-α. It describes its structural features, ligand specificity, gene transcription mechanisms, functional characteristics and target genes. In addition, recent progress with the use of loss of function and gain of function mouse models in the discovery of diverse biological functions of PPAR-α, particularly in the vascular system and the status of the development of new single, dual, pan and partial PPAR agonists (PPAR modulators) in the clinical management of metabolic diseases are presented. This review also summarizes the clinical outcomes from a large number of clinical trials aimed at evaluating the atheroprotective actions of current clinically used PPAR-α agonists, fibrates and statin–fibrate combination therapy.
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