Journal article
Mechanism of sodium channel block by local anesthetics, antiarrhythmics, and anticonvulsants
Abstract
Local anesthetics, antiarrhythmics, and anticonvulsants include both charged and electroneutral compounds that block voltage-gated sodium channels. Prior studies have revealed a common drug-binding region within the pore, but details about the binding sites and mechanism of block remain unclear. Here, we use the x-ray structure of a prokaryotic sodium channel, NavMs, to model a eukaryotic channel and dock representative ligands. These include …
Authors
Tikhonov DB; Zhorov BS
Journal
Journal of General Physiology, Vol. 149, No. 4, pp. 465–481
Publisher
Rockefeller University Press
Publication Date
April 3, 2017
DOI
10.1085/jgp.201611668
ISSN
0022-1295
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AcetamidesAnesthetics, LocalAnimalsAnti-Arrhythmia AgentsAnticonvulsantsBenzhydryl CompoundsBinding SitesCarbamazepineCocaineHumansLacosamideLamotrigineLidocaineMolecular Docking SimulationNAV1.4 Voltage-Gated Sodium ChannelPhenolsPhenytoinPiperazinesProtein BindingPyrimidinesQuinidineSodium Channel BlockersTriazines