HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Augmentation of M-type (KCNQ) potassium channels as a novel strategy to reduce stroke-induced brain injury.

Abstract
Cerebral ischemic stroke is a worldwide cause of mortality/morbidity and thus an important focus of research to decrease the severity of brain injury. Therapeutic options for acute stroke are still limited. In neurons throughout the brain, "M-type" K(+) currents, underlain by KCNQ subunits 2-5, play dominant roles in control over excitability, and are thus implicated in myriad neurological and psychiatric disorders. Although KCNQ channel openers, such as retigabine, have emerged as anti-epilepsy drugs, their effects on ischemic injury remain unknown. Here, we investigated the protective effects of M-channel openers on stroke-induced brain injury in mouse photothrombotic and middle cerebral artery occlusion (MCAo) models. Both photothrombosis and MCAo led to rapid, predictable, and consistently sized necrotic brain lesions, inflammatory responses, and behavioral deficits. Administration of three distinct M-channel openers at 0-6 h after ischemic injury significantly decreased brain infarct size and inflammation, and prevented neurological dysfunction, although they were more effective when administered 0-3 h poststroke. Thus, we show beneficial effects against stroke-induced brain injury and neuronal death through pharmacological regulation of ion channels that control neuronal excitability.
AuthorsSonya M Bierbower, Frank S Choveau, James D Lechleiter, Mark S Shapiro
JournalThe Journal of neuroscience : the official journal of the Society for Neuroscience (J Neurosci) Vol. 35 Issue 5 Pg. 2101-11 (Feb 04 2015) ISSN: 1529-2401 [Electronic] United States
PMID25653366 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
CopyrightCopyright © 2015 the authors 0270-6474/15/352101-11$15.00/0.
Chemical References
  • 10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenone
  • Anthracenes
  • Carbamates
  • KCNQ Potassium Channels
  • Phenylenediamines
  • Potassium Channel Blockers
  • ezogabine
Topics
  • Animals
  • Anthracenes (administration & dosage, pharmacology, therapeutic use)
  • Carbamates (administration & dosage, pharmacology, therapeutic use)
  • Drug Therapy, Combination
  • Infarction, Middle Cerebral Artery (drug therapy)
  • KCNQ Potassium Channels (agonists, antagonists & inhibitors)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Phenylenediamines (administration & dosage, pharmacology, therapeutic use)
  • Potassium Channel Blockers (administration & dosage, pharmacology, therapeutic use)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: