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Physiology and Pathophysiology of Sodium Channel Inactivation.
- Source :
-
Current topics in membranes [Curr Top Membr] 2016; Vol. 78, pp. 479-509. Date of Electronic Publication: 2016 Jul 05. - Publication Year :
- 2016
-
Abstract
- Voltage-gated sodium channels are present in different tissues within the human body, predominantly nerve, muscle, and heart. The sodium channel is composed of four similar domains, each containing six transmembrane segments. Each domain can be functionally organized into a voltage-sensing region and a pore region. The sodium channel may exist in resting, activated, fast inactivated, or slow inactivated states. Upon depolarization, when the channel opens, the fast inactivation gate is in its open state. Within the time frame of milliseconds, this gate closes and blocks the channel pore from conducting any more sodium ions. Repetitive or continuous stimulations of sodium channels result in a rate-dependent decrease of sodium current. This process may continue until the channel fully shuts down. This collapse is known as slow inactivation. This chapter reviews what is known to date regarding, sodium channel inactivation with a focus on various mutations within each NaV subtype and with clinical implications.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Subjects :
- Action Potentials drug effects
Action Potentials physiology
Animals
Central Nervous System metabolism
Central Nervous System physiopathology
Humans
Neurotoxins chemistry
Neurotoxins metabolism
Neurotoxins pharmacology
Protein Isoforms antagonists & inhibitors
Protein Isoforms metabolism
Protein Subunits antagonists & inhibitors
Protein Subunits metabolism
Voltage-Gated Sodium Channel Blockers chemistry
Voltage-Gated Sodium Channel Blockers metabolism
Voltage-Gated Sodium Channel Blockers pharmacology
Voltage-Gated Sodium Channels chemistry
Voltage-Gated Sodium Channels metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1063-5823
- Volume :
- 78
- Database :
- MEDLINE
- Journal :
- Current topics in membranes
- Publication Type :
- Academic Journal
- Accession number :
- 27586293
- Full Text :
- https://doi.org/10.1016/bs.ctm.2016.04.001