Gut-liver axis in the progression of nonalcoholic fatty liver disease: From the microbial derivatives-centered perspective

被引:18
作者
Luo, Lijun
Chang, Yongchun
Sheng, Li
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Dept Drug Metab, Beijing, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing Key Lab Nonclin Drug Metab & PK PD Study, Beijing, Peoples R China
关键词
NAFLD; MAFLD; Microbiota; Derivatives; Metabolites; DIET-INDUCED STEATOHEPATITIS; RECEPTOR 2-DEFICIENT MICE; BILE-ACID SEQUESTRATION; HEPATIC STEATOSIS; URSODEOXYCHOLIC ACID; INSULIN-RESISTANCE; OBETICHOLIC ACID; KUPFFER CELLS; FXR AGONIST; MOUSE MODEL;
D O I
10.1016/j.lfs.2023.121614
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Nonalcoholic fatty liver disease (NAFLD) is one of the world's most common chronic liver diseases. However, its pathogenesis remains unclear. With the deepening of research, NAFLD is considered a metabolic syndrome associated with the environment, heredity, and metabolic disorders. Recently, the close relationship between the intestinal microbiome and NAFLD has been discovered, and the theory of the "gut-liver axis" has been proposed. In short, the gut bacteria directly reach the liver via the portal vein through the damaged intestinal wall or indirectly participate in the development of NAFLD through signaling pathways mediated by their components and metabolites. This review focuses on the roles of microbiota-derived lipopolysaccharide, DNA, peptidoglycan, bile acids, short-chain fatty acids, endogenous ethanol, choline and its metabolites, indole and its derivatives, and bilirubin and its metabolites in the progression of NAFLD, which may provide significative insights into the pathogenesis, diagnosis, and treatment for this highly prevalent liver disease.
引用
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页数:12
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