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Farnesoid X receptor agonist for the treatment of liver and metabolic disorders: focus on 6-ethyl-CDCA.

Abstract
6-ethyl-chedeoxycholic acid (6E-CDCA) is a farnesoid X receptor (FXR) ligand endowed with agonistic activity under development for treatment of cholestatic liver diseases including primary biliary cirrhosis (PBC) and liver-related metabolic disorders including non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH). FXR is a bile sensor that acts in coordination with other nuclear receptors to regulate essential steps of bile acid uptake, metabolism and excretion. 6E-CDCA has been investigated in preclinical models of cholestasis, liver fibrosis and diet-induced atherosclerosis. In a phase II clinical trial in patients with PBC, 6E-CDCA met the primary endpoint of a reduction in alkaline phosphatase levels but safety data indicated that the drug exacerbated pruritus, one of the main symptoms of PBC, suggesting that 6E-CDCA or FXR are mediators of pruritus in humans. Treatment of patients with diabetes and liver steatosis resulted in amelioration of insulin sensitivity despite a reduction a slight reduction in HDL and increased levels of LDL were observed. These side effects on bile acids and lipid metabolism were all predicted by pre-clinical studies, suggesting that potent FXR ligands hold promise but potential side effects might limit their development.
AuthorsS Fiorucci, S Cipriani, A Mencarelli, F Baldelli, G Bifulco, A Zampella
JournalMini reviews in medicinal chemistry (Mini Rev Med Chem) Vol. 11 Issue 9 Pg. 753-62 (Aug 2011) ISSN: 1875-5607 [Electronic] Netherlands
PMID21707532 (Publication Type: Journal Article)
Chemical References
  • Hypoglycemic Agents
  • Receptors, Cytoplasmic and Nuclear
  • obeticholic acid
  • farnesoid X-activated receptor
  • Chenodeoxycholic Acid
Topics
  • Animals
  • Chenodeoxycholic Acid (analogs & derivatives, chemistry, pharmacokinetics, therapeutic use)
  • Clinical Trials as Topic
  • Disease Models, Animal
  • Drug Evaluation, Preclinical
  • Humans
  • Hypoglycemic Agents (chemistry, pharmacokinetics, therapeutic use)
  • Liver Diseases (drug therapy)
  • Metabolic Diseases (drug therapy)
  • Receptors, Cytoplasmic and Nuclear (agonists, metabolism)

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