Fast lidocaine block of cardiac and skeletal muscle sodium channels: one site with two routes of access.
about
Quinine blocks specific gap junction channel subtypesSodium channel molecular conformations and antiarrhythmic drug affinityThe hitchhiker's guide to the voltage-gated sodium channel galaxyHyperkalemic cardioplegia for adult and pediatric surgery: end of an era?Interaction of batrachotoxin with the local anesthetic receptor site in transmembrane segment IVS6 of the voltage-gated sodium channelClassification of drugs based on properties of sodium channel inhibition: a comparative automated patch-clamp studyMolecular determinants of drug access to the receptor site for antiarrhythmic drugs in the cardiac Na+ channel.Charged tetracaine as an inactivation enhancer in batrachotoxin-modified Na+ channels.State-dependent block underlies the tissue specificity of lidocaine action on batrachotoxin-activated cardiac sodium channels.Dual actions of procainamide on batrachotoxin-activated sodium channels: open channel block and prevention of inactivationDissecting lidocaine action: diethylamide and phenol mimic separate modes of lidocaine block of sodium channels from heart and skeletal muscleMolecular action of lidocaine on the voltage sensors of sodium channelsPermeation of large tetra-alkylammonium cations through mutant and wild-type voltage-gated sodium channels as revealed by relief of block at high voltageLocal anesthetics as effectors of allosteric gating. Lidocaine effects on inactivation-deficient rat skeletal muscle Na channels.Novel molecular determinants in the pore region of sodium channels regulate local anesthetic binding.Mechanism of action of sodium channel blocker insecticides (SCBIs) on insect sodium channels.The sodium channel as a target for local anesthetic drugs.Outward stabilization of the S4 segments in domains III and IV enhances lidocaine block of sodium channels.Block of voltage-dependent calcium channels by aliphatic monoamines.Conotoxins as sensors of local pH and electrostatic potential in the outer vestibule of the sodium channel.Amine blockers of the cytoplasmic mouth of sodium channels: a small structural change can abolish voltage dependence.Multiple open channel states revealed by lidocaine and QX-314 on rat brain voltage-dependent sodium channels.Multiple inhibitory actions of lidocaine on Torpedo nicotinic acetylcholine receptors transplanted to Xenopus oocytes.Quaternary ammonium block of mutant Na+ channels lacking inactivation: features of a transition-intermediate mechanism.Protonation state of inhibitors determines interaction sites within voltage-gated sodium channels.
P2860
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P2860
Fast lidocaine block of cardiac and skeletal muscle sodium channels: one site with two routes of access.
description
1993 nî lūn-bûn
@nan
1993 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Fast lidocaine block of cardia ...... ite with two routes of access.
@ast
Fast lidocaine block of cardia ...... ite with two routes of access.
@en
Fast lidocaine block of cardia ...... ite with two routes of access.
@nl
type
label
Fast lidocaine block of cardia ...... ite with two routes of access.
@ast
Fast lidocaine block of cardia ...... ite with two routes of access.
@en
Fast lidocaine block of cardia ...... ite with two routes of access.
@nl
prefLabel
Fast lidocaine block of cardia ...... ite with two routes of access.
@ast
Fast lidocaine block of cardia ...... ite with two routes of access.
@en
Fast lidocaine block of cardia ...... ite with two routes of access.
@nl
P2860
P1433
P1476
Fast lidocaine block of cardia ...... site with two routes of access
@en
P2093
P2860
P356
10.1016/S0006-3495(93)81042-7
P407
P577
1993-07-01T00:00:00Z