The human histamine H3 receptor couples to GIRK channels in Xenopus oocytes

Eur J Pharmacol. 2007 Jul 19;567(3):206-10. doi: 10.1016/j.ejphar.2007.04.032. Epub 2007 Apr 30.

Abstract

The histamine H(3) receptor mediates inhibitory responses in the nervous system. Here, we demonstrate the coupling of the human histamine H(3) receptor to G protein-coupled inward rectifier potassium (GIRK) channels in Xenopus oocytes, using voltage-clamp. The histamine H(3) receptor agonist (R)-alpha-methylhistamine increased GIRK currents with an EC(50) of 2.5 nM. The response to (R)-alpha-methylhistamine was inhibited by the specific antagonist/inverse agonist clobenpropit. GIRK channels represent a novel effector pathway for the histamine H(3) receptor, also suggesting the use of electrophysiology assays in histamine H(3) receptor drug screening, allowing for the resolution of G protein activation kinetics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Electrophysiology
  • G Protein-Coupled Inwardly-Rectifying Potassium Channels / physiology*
  • Histamine Agonists / pharmacology
  • Histamine Antagonists / pharmacology
  • Humans
  • Imidazoles / pharmacology
  • Methylhistamines / pharmacology
  • Oocytes / metabolism*
  • Patch-Clamp Techniques
  • Receptors, Histamine H3 / drug effects
  • Receptors, Histamine H3 / physiology*
  • Thiourea / analogs & derivatives
  • Thiourea / pharmacology
  • Xenopus

Substances

  • G Protein-Coupled Inwardly-Rectifying Potassium Channels
  • Histamine Agonists
  • Histamine Antagonists
  • Imidazoles
  • Methylhistamines
  • Receptors, Histamine H3
  • alpha-methylhistamine
  • Thiourea
  • clobenpropit