核受体
过氧化物酶体增殖物激活受体
受体
转录因子
葡萄糖稳态
炎症
激素
基因亚型
病态的
生物
过氧化物酶体
PPAR激动剂
心肌梗塞
过氧化物酶体增殖物激活受体δ
内科学
生物信息学
内分泌学
医学
生物化学
胰岛素抵抗
糖尿病
基因
作者
Kay‐Dietrich Wagner,Nicole Wagner
摘要
Peroxisome proliferator-activated receptors (PPARs) belong to the nuclear hormone receptor family. They are ligand-activated transcription factors and exist in three different isoforms, PPARα (NR1C1), PPARβ/δ (NR1C2), and PPARγ (NR1C3). PPARs regulate a variety of functions, including glucose and lipid homeostasis, inflammation, and development. They exhibit tissue and cell type-specific expression patterns and functions. Besides the established notion of the therapeutic potential of PPAR agonists for the treatment of glucose and lipid disorders, more recent data propose specific PPAR ligands as potential therapies for cardiovascular diseases. In this review, we focus on the knowledge of PPAR function in myocardial infarction, a severe pathological condition for which therapeutic use of PPAR modulation has been suggested.
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