The peroxisome proliferator-activated receptors in cardiovascular diseases: experimental benefits and clinical challenges

被引:66
作者
Cheang, Wai San [1 ,2 ]
Tian, Xiao Yu [3 ]
Wong, Wing Tak [3 ]
Huang, Yu [1 ,2 ]
机构
[1] Chinese Univ Hong Kong, Shenzhen Res Inst, Inst Vasc Med, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, Hong Kong, Hong Kong, Peoples R China
[3] Houston Methodist Res Inst, Dept Cardiovasc Sci, Houston, TX USA
关键词
TYPE-2; DIABETES-MELLITUS; PROTECTS ENDOTHELIAL FUNCTION; PPAR-ALPHA/GAMMA AGONIST; E-KNOCKOUT MICE; MYOCARDIAL-INFARCTION; GAMMA-AGONIST; DELTA AGONIST; CONCISE GUIDE; FATTY-ACIDS; ATTENUATES ATHEROSCLEROSIS;
D O I
10.1111/bph.13029
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The peroxisome proliferator-activated receptors, PPAR, PPAR/ and PPAR, are ligand-activated transcriptional factors belonging to the nuclear receptors superfamily and they are known to play important roles in glucose and lipid metabolism. Experimental studies in animal models of metabolic diseases have also revealed that activation of PPARs protects against the vascular complications of diabetes, hypertension, atherosclerosis, myocardial infarction and stroke, through exerting their anti-inflammatory, anti-atherogenic and antioxidant effects. In clinical trials and post-market surveillance, agonists of PPARs have been shown to effectively prevent cardiovascular events. However, adverse effects, particularly for PPAR agonists, are also observed with the use of investigational PPAR agonists and even some approved drugs. Further exploration of underlying mechanisms is needed to develop novel ways of PPAR activation without causing serious side effects. This article reviews the cardiovascular effects of PPARs, with emphasis on the therapeutic potential of PPAR agonists in combating metabolic vascular diseases. Linked ArticlesThis article is part of a themed section on Chinese Innovation in Cardiovascular Drug Discovery. To view the other articles in this section visit http://dx. doi. org/10.1111/bph. 2015.172. issue-23
引用
收藏
页码:5512 / 5522
页数:11
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