KCNQ3 is the principal target of retigabine in CA1 and subicular excitatory neurons
Author:
Affiliation:
1. Department of Physiology and Neurobiology, University of Connecticut, Storrs, Connecticut
2. Department of Neuroscience, University of Naples Federico II, Naples, Italy
Abstract
Funder
HHS | NIH | National Institute of Neurological Disorders and Stroke
HHS | NIH | National Heart, Lung, and Blood Institute
Publisher
American Physiological Society
Subject
Physiology,General Neuroscience
Link
https://journals.physiology.org/doi/pdf/10.1152/jn.00564.2020
Reference40 articles.
1. The mechanism of action of retigabine (ezogabine), a first-in-class K+ channel opener for the treatment of epilepsy
2. Potent KCNQ2/3-Specific Channel Activator Suppresses In Vivo Epileptic Activity and Prevents the Development of Tinnitus
3. Acute Effects of Riluzole and Retigabine on Axonal Excitability in Patients With Amyotrophic Lateral Sclerosis: A Randomized, Double-Blind, Placebo-Controlled, Crossover Trial
4. Ezogabine (KCNQ2/3 channel opener) prevents delayed activation of meningeal nociceptors if given before but not after the occurrence of cortical spreading depression
5. Neuropathic pain and Kv7 voltage-gated potassium channels: The potential role of Kv7 activators in the treatment of neuropathic pain
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3. Combinations of classical and non-classical voltage dependent potassium channel openers suppress nociceptor discharge and reverse chronic pain signs in a rat model of Gulf War illness;NeuroToxicology;2022-12
4. Removal of KCNQ2 from parvalbumin-expressing interneurons improves anti-seizure efficacy of retigabine;Experimental Neurology;2022-09
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