Nuclear receptors as drug targets in cholestatic liver diseases

Clin Liver Dis. 2013 May;17(2):161-89. doi: 10.1016/j.cld.2012.12.001.

Abstract

Cholestatic liver diseases encompass a wide spectrum of disorders with different causes, resulting in impaired bile flow and accumulation of bile acids and other potentially hepatotoxic cholephils. The understanding of the molecular mechanisms of bile formation and cholestasis has recently improved significantly through new insights into nuclear receptor (patho)biology. Nuclear receptors are ligand-activated transcription factors, which act as central players in the regulation of genes responsible for elimination and detoxification of biliary constituents accumulating in cholestasis. They also control other pathophysiologic processes such as inflammation, fibrogenesis, and carcinogenesis involved in the pathogenesis and disease progression of cholestasis liver diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Bile Acids and Salts / biosynthesis*
  • Cholagogues and Choleretics / therapeutic use
  • Cholestasis / drug therapy*
  • Cholestasis / genetics
  • Cholestasis / metabolism*
  • Constitutive Androstane Receptor
  • Homeostasis / drug effects
  • Humans
  • Ligands
  • Peroxisome Proliferator-Activated Receptors / metabolism
  • Pregnane X Receptor
  • Receptors, Calcitriol / genetics
  • Receptors, Calcitriol / metabolism
  • Receptors, Cytoplasmic and Nuclear / agonists
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Receptors, Glucocorticoid / metabolism
  • Receptors, Steroid / genetics
  • Receptors, Steroid / metabolism
  • Signal Transduction / drug effects*
  • Signal Transduction / genetics
  • Ursodeoxycholic Acid / therapeutic use

Substances

  • Bile Acids and Salts
  • Cholagogues and Choleretics
  • Constitutive Androstane Receptor
  • Ligands
  • Peroxisome Proliferator-Activated Receptors
  • Pregnane X Receptor
  • Receptors, Calcitriol
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Glucocorticoid
  • Receptors, Steroid
  • farnesoid X-activated receptor
  • Ursodeoxycholic Acid