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Antipsychotics inhibit TREK but not TRAAK channels.

AbstractSchizophrenia is a chronic mental illness affecting 0.4% of the population. Existing antipsychotic drugs are mainly used to treat positive symptoms such as hallucinations but have only poor effects on negative symptoms such as cognitive deficits or depression. TREK and TRAAK channels are two P domain background potassium channels activated by polyunsaturated fatty acids and mechanical stress. TREK but not TRAAK channels are regulated by Gs- and Gq-coupled pathways. The inactivation of the TREK-1 but not the TRAAK channel in mice results in a depression-resistant phenotype. In addition, it has been shown that antidepressants such as fluoxetine or paroxetine directly inhibit TREK channel activity. Here we show that different antipsychotic drugs directly inhibit TREK currents with IC(50) values of approximately 1 to approximately 20 microM. No effect is seen on TRAAK channel activity. We conclude that TREK channels might be involved in the therapeutic action of antipsychotics or in their secondary effects. Furthermore, TREK channels could play a role in the pathophysiology of psychiatric disorders such as depression and schizophrenia.
AuthorsSusanne Thümmler, Fabrice Duprat, Michel Lazdunski (Affiliation: Institut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique, UMR 6097, Université de Nice-Sophia Antipolis, 660 Route des Lucioles, Sophia-Antipolis, 06560 Valbonne, France.)
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 354 Issue 1 Pg. 284-9 (Mar 2 2007) ISSN: 0006-291X United States
PMID17222806 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antipsychotic Agents
  • KCNK4 protein, human
  • Potassium Channels
  • Potassium Channels, Tandem Pore Domain
  • potassium channel protein TREK-1
Topics
  • Animals
  • Antipsychotic Agents (administration & dosage)
  • COS Cells
  • Cercopithecus aethiops
  • Dose-Response Relationship, Drug
  • Ion Channel Gating (drug effects, physiology)
  • Membrane Potentials (physiology)
  • Potassium Channels (drug effects, physiology)
  • Potassium Channels, Tandem Pore Domain (antagonists & inhibitors, drug effects, physiology)