Farnesoid X Receptor an Emerging Target to Combat Obesity

Dig Dis. 2017;35(3):185-190. doi: 10.1159/000450909. Epub 2017 Mar 1.

Abstract

Obesity and its associated diseases, including type 2 diabetes, have reached epidemic levels worldwide. However, available treatment options are limited and ineffective in managing the disease. There is therefore an urgent need for the development of new pharmacological solutions. The bile acid (BA) Farnesoid X receptor (FXR) has recently emerged as an attractive candidate. Initially described for their role in lipid and vitamin absorption from diet, BAs are hormones with powerful effects on whole body lipid and glucose metabolism. In this review, we focus on FXR and how 2 decades of work on this receptor, both in rodents and humans, have led to the development of drug agonists with potential use in humans for treatment of conditions ranging from obesity-associated diseases to BA dysregulation.

Publication types

  • Review

MeSH terms

  • Animals
  • Benzene Derivatives / therapeutic use
  • Bile Acids and Salts / biosynthesis
  • Bile Acids and Salts / blood
  • Humans
  • Molecular Targeted Therapy*
  • Obesity / drug therapy
  • Obesity / metabolism*
  • Receptors, Cytoplasmic and Nuclear / agonists
  • Receptors, Cytoplasmic and Nuclear / metabolism*

Substances

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