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

Biochim Biophys Acta. 2010 Jul;1801(7):683-92. doi: 10.1016/j.bbalip.2010.04.006. Epub 2010 Apr 23.

Abstract

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.

Publication types

  • Review

MeSH terms

  • Animals
  • Bacterial Translocation
  • Bile / metabolism
  • Bile Acids and Salts / metabolism*
  • Gastrointestinal Diseases / metabolism*
  • Gastrointestinal Diseases / physiopathology
  • Humans
  • Intestinal Mucosa / metabolism
  • Intestines / physiopathology
  • Liver / metabolism
  • Liver / physiopathology
  • Liver Diseases / metabolism*
  • Liver Diseases / physiopathology
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Regeneration

Substances

  • Bile Acids and Salts
  • Receptors, Cytoplasmic and Nuclear
  • farnesoid X-activated receptor