A novel therapeutic target, GPR43; where it stands in drug discovery

Arch Pharm Res. 2012 Sep;35(9):1505-9. doi: 10.1007/s12272-012-0900-6.

Abstract

With growing interest in human microbiome for its implication in metabolic disorders, inflammatory diseases, immune disorders and so forth, understanding the biology at the interface of the gut flora and the host becomes very important for identifying novel therapeutic avenues. GPR43 has been deorphanized and the metabolites of microbiome, such as short-chain fatty acids, serve as its natural ligands. There are numerous reports that GPR43 might be a crucial link to the novel therapies for the unmet medical needs and many drug discovery organizations are making their moves in response.

Publication types

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

MeSH terms

  • Adipogenesis / drug effects*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Drug Discovery
  • Drugs, Investigational / pharmacology*
  • Drugs, Investigational / therapeutic use
  • Humans
  • Ligands
  • Lipolysis / drug effects*
  • Metabolic Syndrome / drug therapy
  • Metabolic Syndrome / metabolism
  • Molecular Targeted Therapy
  • Overweight / drug therapy
  • Overweight / immunology
  • Overweight / metabolism
  • Receptors, Cell Surface / agonists*
  • Receptors, Cell Surface / antagonists & inhibitors*
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Drugs, Investigational
  • FFA2R protein, human
  • Ligands
  • Receptors, Cell Surface