PPAR激动剂
过氧化物酶体增殖物激活受体
炎症
脂质代谢
受体
核受体
生物
阿尔法(金融)
细胞因子
葡萄糖稳态
平衡
兴奋剂
过氧化物酶体增殖物激活受体δ
内分泌学
转录因子
内科学
药理学
免疫学
医学
胰岛素抵抗
生物化学
糖尿病
基因
护理部
患者满意度
结构效度
作者
Caroline Duval,Giulia Chinetti,François Trottein,Jean‐Charles Fruchart,Bart Staels
标识
DOI:10.1016/s1471-4914(02)02385-7
摘要
Peroxisome proliferator-activated receptors (PPARs) are lipid-activated transcription factors that regulate lipid and lipoprotein metabolism, glucose homeostasis and inflammation. The PPAR family consists of three proteins, alpha, beta/delta and gamma. Recent data suggest that PPAR alpha and gamma activation decreases atherosclerosis progression not only by correcting metabolic disorders, but also through direct effects on the vascular wall. PPARs modulate the recruitment of leukocytes to endothelial cells, control the inflammatory response and lipid homeostasis of monocytes/macrophages and regulate inflammatory cytokine production by smooth muscle cells. Experiments using animal models of atherosclerosis and clinical studies in humans strongly support an anti-atherosclerotic role for PPAR alpha and gamma in vivo. Thus, PPARs remain attractive therapeutic targets for the development of drugs used in the treatment of chronic inflammatory diseases such as atherosclerosis. Future research will aim for the development of more potent drugs with co-agonist activity on PPAR alpha, PPAR beta/delta and/or PPAR gamma as well as tissue and target gene-selective PPAR receptor modulators (SPPARMs).
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