GPR120 agonism as a countermeasure against metabolic diseases

Drug Discov Today. 2014 May;19(5):670-9. doi: 10.1016/j.drudis.2013.11.021. Epub 2013 Dec 4.

Abstract

Obesity, type 2 diabetes mellitus and cardiovascular disease are at epidemic proportions in developed nations globally, representing major causes of ill-health and premature death. The search for drug targets to counter the growing prevalence of metabolic diseases has uncovered G-protein-coupled receptor 120 (GPR120). GPR120 agonism has been shown to improve inflammation and metabolic health on a systemic level via regulation of adiposity, gastrointestinal peptide secretion, taste preference and glucose homeostasis. Therefore, GPR120 agonists present as a novel therapeutic option that could be exploited for the treatment of impaired metabolic health. This review summarizes the current knowledge of GPR120 functionality and the potential applications of GPR120-specific agonists for the treatment of disease states such as obesity, type 2 diabetes mellitus and cardiovascular disease.

Publication types

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

MeSH terms

  • Animals
  • Biphenyl Compounds / chemistry
  • Biphenyl Compounds / pharmacology
  • Biphenyl Compounds / therapeutic use
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / metabolism
  • Humans
  • Metabolic Diseases / drug therapy*
  • Metabolic Diseases / metabolism
  • Obesity / drug therapy
  • Obesity / metabolism
  • Phenylpropionates / chemistry
  • Phenylpropionates / pharmacology
  • Phenylpropionates / therapeutic use
  • Receptors, G-Protein-Coupled / agonists*
  • Receptors, G-Protein-Coupled / metabolism

Substances

  • 3-(4-((4-fluoro-4'-methyl-(1,1'-biphenyl)-2-yl)methoxy)phenyl)propanoic acid
  • Biphenyl Compounds
  • FFAR4 protein, human
  • Phenylpropionates
  • Receptors, G-Protein-Coupled