Essential roles of bile acids and their nuclear receptors, FXR and PXR, in the cholestatic liver disease

被引:3
|
作者
Han, Bumin [1 ]
Kim, Byung-Kwon [1 ]
Kim, Kyumin [1 ]
Fang, Sungsoon [1 ]
机构
[1] Sejong Univ, Coll Life Sci, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Bile acids; Farnesoid X receptor; Pregnane X receptor; PRIMARY BILIARY-CIRRHOSIS; URSODEOXYCHOLIC ACID; HCO3-UMBRELLA; PATHOGENESIS; INJURY;
D O I
10.1080/19768354.2016.1211175
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Bile acids (BAs) are steroid acids found predominantly in the bile of mammals and other vertebrates. Though BAs have been known as digestive juice, recent studies have revealed that BAs act as signaling molecules to control metabolism and inflammation. Today, BAs are considered as potential therapeutic molecules for treatment of complex metabolic liver disease. However, the detergent properties of BAs lead to hepatic injury and intrahepatic cholestasis when BAs are accumulated in the liver with impaired bile flow into gall bladder. Cholestasis is a pathological condition of hepatic retention of cytotoxic bile acids. To date, hydrophilic ursodeoxycholic acid has been currently used to treat cholestasis, but the efficacy of UDCA for cholestasis is still limited. Given that BAs are endogenous ligands of several nuclear receptors, including Farnesoid X receptor and Pregnane X receptor, novel synthetic ligands for those nuclear receptors are promising for the treatment of cholestatic liver diseases.
引用
收藏
页码:175 / 178
页数:4
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