非酒精性脂肪肝
发病机制
脂肪肝
过氧化物酶体增殖物激活受体
胰岛素抵抗
炎症
脂肪生成
脂质代谢
核受体
医学
氧化应激
生物
内科学
内分泌学
转录因子
生物信息学
疾病
癌症研究
受体
糖尿病
脂肪组织
生物化学
基因
作者
Hao Chen,Huabing Tan,Juan Wan,Yong Zeng,Jincheng Wang,Haichuan Wang,Xiaojie Lu
标识
DOI:10.1016/j.pharmthera.2023.108391
摘要
Non-alcoholic fatty liver disease (NAFLD), currently the leading cause of global chronic liver disease, has emerged as a major public health problem, more efficient therapeutics of which are thus urgently needed. Peroxisome proliferator-activated receptor γ (PPAR-γ), ligand-activated transcription factors of the nuclear hormone receptor superfamily, is considered a crucial metabolic regulator of hepatic lipid metabolism and inflammation. The role of PPAR-γ in the pathogenesis of NAFLD is gradually being recognized. Here, we outline the involvement of PPAR-γ in the pathogenesis of NAFLD through adipogenesis, insulin resistance, inflammation, oxidative stress, endoplasmic reticulum stress, and fibrosis. In addition, the evidence for PPAR-γ- targeted therapy for NAFLD are summarized. Altogether, PPAR-γ is a promising therapeutic target for NAFLD, and the development of drugs that can balance the beneficial and undesirable effects of PPAR-γ will bring new light to NAFLD patients.
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