法尼甾体X受体
G蛋白偶联胆汁酸受体
内科学
脂肪变性
内分泌学
非酒精性脂肪肝
胆汁酸
硼胆酸
脂肪性肝炎
脂肪肝
炎症
生物
核受体
兴奋剂
受体
医学
生物化学
基因
转录因子
疾病
作者
Xiaoxin X. Wang,Cen Xie,Andrew E. Libby,Suman Ranjit,Jonathan Levi,Komuraiah Myakala,Kanchan Bhasin,Bryce A. Jones,David J. Orlicky,Shogo Takahashi,Alexander Dvornikov,David E. Kleiner,Stephen M. Hewitt,Luciano Adorini,Jeffrey B. Kopp,Kristopher W. Krausz,Avi Z. Rosenberg,James L. McManaman,Charles E. Robertson,Diana Ir,Daniel N. Frank,Yuhuan Luo,Frank J. Gonzalez,Enrico Gratton,Moshe Levi
标识
DOI:10.1016/j.jbc.2022.102530
摘要
Nonalcoholic steatohepatitis (NASH) is the most common chronic liver disease in the US, partly due to the increasing incidence of metabolic syndrome, obesity, and type 2 diabetes. The roles of bile acids and their receptors, such as the nuclear receptor farnesoid X receptor (FXR) and the G protein-coupled receptor TGR5, on the development of NASH are not fully clear. C57BL/6J male mice fed a Western diet (WD) develop characteristics of NASH, allowing determination of the effects of FXR and TGR5 agonists on this disease. Here we show that the FXR-TGR5 dual agonist INT-767 prevents progression of WD-induced hepatic steatosis, inflammation, and fibrosis, as determined by histological and biochemical assays and novel label-free microscopy imaging techniques, including third harmonic generation, second harmonic generation, and fluorescence lifetime imaging microscopy. Furthermore, we show INT-767 decreases liver fatty acid synthesis and fatty acid and cholesterol uptake, as well as liver inflammation. INT-767 markedly changed bile acid composition in the liver and intestine, leading to notable decreases in the hydrophobicity index of bile acids, known to limit cholesterol and lipid absorption. In addition, INT-767 upregulated expression of liver p-AMPK, SIRT1, PGC-1α, and SIRT3, which are master regulators of mitochondrial function. Finally, we found INT-767 treatment reduced WD-induced dysbiosis of gut microbiota. Interestingly, the effects of INT-767 in attenuating NASH were absent in FXR-null mice, but still present in TGR5-null mice. Our findings support treatment and prevention protocols with the dual FXR-TGR5 agonist INT-767 arrest progression of WD-induced NASH in mice mediated by FXR-dependent, TGR5-independent mechanisms.