Bile acids and their nuclear receptor FXR: Relevance for hepatobiliary and gastrointestinal disease

被引:168
作者
Gadaleta, Raffaella M. [1 ,2 ,3 ]
van Mil, Saskia W. C. [2 ]
Oldenburg, Bas [1 ]
Siersema, Peter D. [1 ]
Klomp, Leo W. J. [2 ]
van Erpecum, Karel J. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Gastroenterol & Hepatol, NL-3508 GA Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Metab & Endocrine Dis, NL-3508 GA Utrecht, Netherlands
[3] Consorzio Mario Negri Sud, Lab Lipid Metab & Canc, Sta Maria Imbaro, Ch, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2010年 / 1801卷 / 07期
关键词
Bile acid; Carcinogenesis; Enterohepatic circulation; Farnesoid X Receptor; Inflammation; FARNESOID-X-RECEPTOR; FAMILIAL INTRAHEPATIC CHOLESTASIS; NEGATIVE FEEDBACK-REGULATION; SALT EXPORT PUMP; ALPHA-OST-BETA; NF-KAPPA-B; CANALICULAR MEMBRANE; BARRETTS-ESOPHAGUS; ATP8B1; DEFICIENCY; BINDING-PROTEIN;
D O I
10.1016/j.bbalip.2010.04.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The nuclear receptor Farnesoid X Receptor (FXR) critically regulates nascent bile formation and bile acid enterohepatic circulation. Bile acids and FXR play a pivotal role in regulating hepatic inflammation and regeneration as well as in regulating extent of inflammatory responses, barrier function and prevention of bacterial translocation in the intestinal tract. Recent evidence suggests, that the bile acid-FXR interaction is involved in the pathophysiology of a wide range of diseases of the liver, biliary and gastrointestinal tract, such as cholestatic and inflammatory liver diseases and hepatocellular carcinoma, inflammatory bowel disease and inflammation-associated cancer of the colon and esophagus. In this review we discuss current knowledge of the role the bile acid-FXR interaction has in (patho)physiology of the liver, biliary and gastrointestinal tract, and proposed underlying mechanisms, based on in vitro data and experimental animal models. Given the availability of highly potent synthetic FXR agonists, we focus particularly on potential relevance for human disease. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:683 / 692
页数:10
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