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A-Type K(V) Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction
A-type voltage-gated potassium (Kv) channels are major regulators of neuronal excitability that have been mainly characterized in the central nervous system. By contrast, there is a paucity of knowledge about the molecular physiology of these Kv channels in the peripheral nervous system, including h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6088260/ https://www.ncbi.nlm.nih.gov/pubmed/30127716 http://dx.doi.org/10.3389/fnmol.2018.00253 |
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author | Zemel, Benjamin M. Ritter, David M. Covarrubias, Manuel Muqeem, Tanziyah |
author_facet | Zemel, Benjamin M. Ritter, David M. Covarrubias, Manuel Muqeem, Tanziyah |
author_sort | Zemel, Benjamin M. |
collection | PubMed |
description | A-type voltage-gated potassium (Kv) channels are major regulators of neuronal excitability that have been mainly characterized in the central nervous system. By contrast, there is a paucity of knowledge about the molecular physiology of these Kv channels in the peripheral nervous system, including highly specialized and heterogenous dorsal root ganglion (DRG) neurons. Although all A-type Kv channels display pore-forming subunits with similar structural properties and fast inactivation, their voltage-, and time-dependent properties and modulation are significantly different. These differences ultimately determine distinct physiological roles of diverse A-type Kv channels, and how their dysfunction might contribute to neurological disorders. The importance of A-type Kv channels in DRG neurons is highlighted by recent studies that have linked their dysfunction to persistent pain sensitization. Here, we review the molecular neurophysiology of A-type Kv channels with an emphasis on those that have been identified and investigated in DRG nociceptors (Kv1.4, Kv3.4, and Kv4s). Also, we discuss evidence implicating these Kv channels in neuropathic pain resulting from injury, and present a perspective of outstanding challenges that must be tackled in order to discover novel treatments for intractable pain disorders. |
format | Online Article Text |
id | pubmed-6088260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60882602018-08-20 A-Type K(V) Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction Zemel, Benjamin M. Ritter, David M. Covarrubias, Manuel Muqeem, Tanziyah Front Mol Neurosci Neuroscience A-type voltage-gated potassium (Kv) channels are major regulators of neuronal excitability that have been mainly characterized in the central nervous system. By contrast, there is a paucity of knowledge about the molecular physiology of these Kv channels in the peripheral nervous system, including highly specialized and heterogenous dorsal root ganglion (DRG) neurons. Although all A-type Kv channels display pore-forming subunits with similar structural properties and fast inactivation, their voltage-, and time-dependent properties and modulation are significantly different. These differences ultimately determine distinct physiological roles of diverse A-type Kv channels, and how their dysfunction might contribute to neurological disorders. The importance of A-type Kv channels in DRG neurons is highlighted by recent studies that have linked their dysfunction to persistent pain sensitization. Here, we review the molecular neurophysiology of A-type Kv channels with an emphasis on those that have been identified and investigated in DRG nociceptors (Kv1.4, Kv3.4, and Kv4s). Also, we discuss evidence implicating these Kv channels in neuropathic pain resulting from injury, and present a perspective of outstanding challenges that must be tackled in order to discover novel treatments for intractable pain disorders. Frontiers Media S.A. 2018-08-06 /pmc/articles/PMC6088260/ /pubmed/30127716 http://dx.doi.org/10.3389/fnmol.2018.00253 Text en Copyright © 2018 Zemel, Ritter, Covarrubias and Muqeem. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Zemel, Benjamin M. Ritter, David M. Covarrubias, Manuel Muqeem, Tanziyah A-Type K(V) Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction |
title | A-Type K(V) Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction |
title_full | A-Type K(V) Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction |
title_fullStr | A-Type K(V) Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction |
title_full_unstemmed | A-Type K(V) Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction |
title_short | A-Type K(V) Channels in Dorsal Root Ganglion Neurons: Diversity, Function, and Dysfunction |
title_sort | a-type k(v) channels in dorsal root ganglion neurons: diversity, function, and dysfunction |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6088260/ https://www.ncbi.nlm.nih.gov/pubmed/30127716 http://dx.doi.org/10.3389/fnmol.2018.00253 |
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