Literature DB >> 31471460

Role of Voltage-Gated Sodium Channels in the Mechanism of Ether-Induced Unconsciousness.

Nicholas Denomme1, Jacob M Hull1, George A Mashour2.   

Abstract

Despite continuous clinical use for more than 170 years, the mechanism of general anesthetics has not been completely characterized. In this review, we focus on the role of voltage-gated sodium channels in the sedative-hypnotic actions of halogenated ethers, describing the history of anesthetic mechanisms research, the basic neurobiology and pharmacology of voltage-gated sodium channels, and the evidence for a mechanistic interaction between halogenated ethers and sodium channels in the induction of unconsciousness. We conclude with a more integrative perspective of how voltage-gated sodium channels might provide a critical link between molecular actions of the halogenated ethers and the more distributed network-level effects associated with the anesthetized state across species.
Copyright © 2019 by The Author(s).

Entities:  

Year:  2019        PMID: 31471460     DOI: 10.1124/pr.118.016592

Source DB:  PubMed          Journal:  Pharmacol Rev        ISSN: 0031-6997            Impact factor:   25.468


  3 in total

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3.  The T-type calcium channel isoform Cav3.1 is a target for the hypnotic effect of the anaesthetic neurosteroid (3β,5β,17β)-3-hydroxyandrostane-17-carbonitrile.

Authors:  Tamara Timic Stamenic; Simon Feseha; Francesca M Manzella; Damon Wallace; Davis Wilkey; Timothy Corrigan; Hanna Fiedler; Patricia Doerr; Kathiresan Krishnan; Yogendra H Raol; Douglas F Covey; Vesna Jevtovic-Todorovic; Slobodan M Todorovic
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  3 in total

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