肝肠循环
脂肪性肝炎
内科学
脂肪变性
胆汁酸
内分泌学
FGF19型
G蛋白偶联胆汁酸受体
化学
脂肪肝
生物
医学
受体
成纤维细胞生长因子
疾病
作者
Justine Gillard,Laure‐Alix Clerbaux,Maxime Nachit,Christine Sempoux,Bart Staels,Laure B. Bindels,Anne Tailleux,Isabelle A. Leclercq
出处
期刊:JHEP reports
[Elsevier BV]
日期:2021-10-14
卷期号:4 (1): 100387-100387
被引量:92
标识
DOI:10.1016/j.jhepr.2021.100387
摘要
This study clearly demonstrates that the alterations of enterohepatic bile acids significantly contribute to the development of non-alcoholic steatohepatitis in relevant preclinical models. Indeed, experimental modulation of bile acid composition restored perturbed FXR and TGR5 signaling and prevented non-alcoholic steatohepatitis and associated metabolic disorders.
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