FXR Agonists as Therapeutic Agents for Non-alcoholic Fatty Liver Disease

被引:100
|
作者
Carr, Rotonya M. [1 ]
Reid, Andrea E. [2 ]
机构
[1] Univ Penn, Div Gastroenterol, Philadelphia, PA 19104 USA
[2] Washington DC VA Med Ctr, Gastroenterol Hepatol & Nutr Sect, Washington, DC 20422 USA
基金
美国国家卫生研究院;
关键词
FXR; Obetacholic acid; Bile acid; NAFLD; NASH; Alcoholic hepatitis; FARNESOID-X-RECEPTOR; PLACEBO-CONTROLLED TRIAL; BILE-ACID RECEPTOR; HEPATIC STEATOSIS; NUCLEAR RECEPTOR; INSULIN-RESISTANCE; VITAMIN-E; URSODEOXYCHOLIC ACID; METABOLIC SYNDROME; OBETICHOLIC ACID;
D O I
10.1007/s11883-015-0500-2
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Non-alcoholic fatty liver disease (NAFLD) is the hepatic manifestation of the metabolic syndrome and a risk factor for both cardiovascular and hepatic related morbidity and mortality. The increasing prevalence of this disease requires novel therapeutic approaches to prevent disease progression. Farnesoid X receptors are bile acid receptors with roles in lipid, glucose, and energy homeostasis. Synthetic farnesoid X receptor (FXR) agonists have been developed to specifically target these receptors for therapeutic use in NAFL D patients. Here, we present a review of bile acid physiology and how agonismof FXR receptors has been examined in preclinical and clinical NAFLD. Early evidence suggests a potential role for synthetic FXR agonists in the management of NAFLD; however, additional studies are needed to clarify their effects on lipid and glucose parameters in humans.
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收藏
页数:14
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