非酒精性脂肪肝
胰岛素抵抗
内科学
内分泌学
安普克
脂肪变性
血脂异常
脂肪肝
氧化应激
医学
脂质代谢
炎症
糖尿病
生物
疾病
生物化学
酶
蛋白激酶A
作者
Lijuan Liu,Weiming Sun,Xulei Tang,Donghu Zhen,Conghui Guan,Songbo Fu,Jinjin Liu
标识
DOI:10.1016/j.mce.2024.112337
摘要
Nonalcoholic fatty liver disease (NAFLD) is one of the most common chronic liver diseases worldwide; however, effective intervention strategies for NAFLD are still unavailable. The present study sought to investigate the efficacy of chiglitazar, a pan-PPAR agonist, in protecting against NAFLD in mice and its underlying molecular mechanism. Male C57BL/6 J mice were fed a high-fat diet (HFD) for 8 weeks to generate NAFLD and the HFD was continued for an additional 10 weeks in the absence or presence of 5 mg/kg/d or 10 mg/kg/d chiglitazar by gavage. Chiglitazar significantly improved dyslipidemia and insulin resistance, ameliorated hepatic steatosis and reduced liver inflammation and oxidative stress in NAFLD mice. RNA-seq revealed that chiglitazar alleviated HFD-induced NAFLD in mice through multiple pathways, including fatty acid metabolism regulation, insulin signaling pathway, and AMPK signaling pathway. This study demonstrated the potential therapeutic effect of chiglitazar on NAFLD. Chiglitazar ameliorated NAFLD by modulating multiple pathways.
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