GLP-1 receptor agonists: effects on the progression of non-alcoholic fatty liver disease

被引:33
作者
Liu, Jia [1 ]
Wang, Guang [1 ]
Jia, Yumei [1 ]
Xu, Yuan [1 ]
机构
[1] Capital Med Univ, Beijing Chaoyang Hosp, Dept Endocrinol, Beijing 100020, Peoples R China
关键词
non-alcoholic fatty liver disease; glucagon-like peptide-1; lipid metabolism; GLUCAGON-LIKE PEPTIDE-1; DIET-INDUCED OBESITY; HEPATIC STEATOSIS; INSULIN-RESISTANCE; OXIDATIVE STRESS; STEATOHEPATITIS; ADIPONECTIN; CELLS; RISK; PATHOGENESIS;
D O I
10.1002/dmrr.2580
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Non-alcoholic fatty liver disease (NAFLD) is one of the most common liver diseases, and its incidence has been increasing recently. In addition to hepatic complications, NAFLD is also recognized as an independent risk factor for cardiovascular disease. Unfortunately, the current therapies for NAFLD display variable efficacy; a novel and effective drug is urgently needed. Glucagon-like peptide-1 (GLP-1), a receptor agonist is a new drug approved for treating type 2 diabetes. Recently, these types of agents have shown a novel therapeutic effect on NAFLD. However, the mechanisms of GLP-1 receptor agonists on the treatment of NAFLD have not yet been explained precisely. Recent studies have demonstrated that GLP-1 reverses the progression of NAFLD not only indirectly through an incretin effect that improves key parameters involved in NAFLD, but also a direct effect on lipid metabolism of hepatocytes and inflammation in liver. In this review, we provided an overview of the role and mechanisms of GLP-1 in the therapy of NAFLD. Copyright (c) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:329 / 335
页数:7
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