过氧化物酶体增殖物激活受体
葡萄糖稳态
过氧化物酶体
脂质代谢
生物
内分泌学
脂肪肝
受体
内科学
生物信息学
能量稳态
核受体
平衡
糖尿病
疾病
生物化学
胰岛素抵抗
医学
转录因子
基因
作者
Vanessa Dubois,Jérôme Eeckhoute,Philippe Lefèbvre,Bart Staels
摘要
Peroxisome proliferator–activated receptors (PPARs) regulate energy metabolism and hence are therapeutic targets in metabolic diseases such as type 2 diabetes and non-alcoholic fatty liver disease. While they share anti-inflammatory activities, the PPAR isotypes distinguish themselves by differential actions on lipid and glucose homeostasis. In this Review we discuss the complementary and distinct metabolic effects of the PPAR isotypes together with the underlying cellular and molecular mechanisms, as well as the synthetic PPAR ligands that are used in the clinic or under development. We highlight the potential of new PPAR ligands with improved efficacy and safety profiles in the treatment of complex metabolic disorders.
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