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Polyunsaturated Fatty Acids as Modulators of K(V)7 Channels

Voltage-gated potassium channels of the K(V)7 family are expressed in many tissues. The physiological importance of K(V)7 channels is evident from specific forms of disorders linked to dysfunctional K(V)7 channels, including variants of epilepsy, cardiac arrhythmia and hearing impairment. Thus, unde...

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Autores principales: Larsson, Johan E., Frampton, Damon J. A., Liin, Sara I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300222/
https://www.ncbi.nlm.nih.gov/pubmed/32595524
http://dx.doi.org/10.3389/fphys.2020.00641
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author Larsson, Johan E.
Frampton, Damon J. A.
Liin, Sara I.
author_facet Larsson, Johan E.
Frampton, Damon J. A.
Liin, Sara I.
author_sort Larsson, Johan E.
collection PubMed
description Voltage-gated potassium channels of the K(V)7 family are expressed in many tissues. The physiological importance of K(V)7 channels is evident from specific forms of disorders linked to dysfunctional K(V)7 channels, including variants of epilepsy, cardiac arrhythmia and hearing impairment. Thus, understanding how K(V)7 channels are regulated in the body is of great interest. This Mini Review focuses on the effects of polyunsaturated fatty acids (PUFAs) on K(V)7 channel activity and possible underlying mechanisms of action. By summarizing reported effects of PUFAs on K(V)7 channels and native K(V)7-mediated currents, we conclude that the generally observed effect is a PUFA-induced increase in current amplitude. The increase in current is commonly associated with a shift in the voltage-dependence of channel opening and in some cases with increased maximum conductance. Auxiliary KCNE subunits, which associate with K(V)7 channels in certain tissues, may influence PUFA effects, though findings are conflicting. Both direct and indirect activating PUFA effects have been described, direct effects having been most extensively studied on K(V)7.1. The negative charge of the PUFA head-group has been identified as critical for electrostatic interaction with conserved positively charged amino acids in transmembrane segments 4 and 6. Additionally, the localization of double bonds in the PUFA tail tunes the apparent affinity of PUFAs to K(V)7.1. Indirect effects include those mediated by PUFA metabolites. Indirect inhibitory effects involve K(V)7 channel degradation and re-distribution from lipid rafts. Understanding how PUFAs regulate K(V)7 channels may provide insight into physiological regulation of K(V)7 channels and bring forth new therapeutic strategies.
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spelling pubmed-73002222020-06-26 Polyunsaturated Fatty Acids as Modulators of K(V)7 Channels Larsson, Johan E. Frampton, Damon J. A. Liin, Sara I. Front Physiol Physiology Voltage-gated potassium channels of the K(V)7 family are expressed in many tissues. The physiological importance of K(V)7 channels is evident from specific forms of disorders linked to dysfunctional K(V)7 channels, including variants of epilepsy, cardiac arrhythmia and hearing impairment. Thus, understanding how K(V)7 channels are regulated in the body is of great interest. This Mini Review focuses on the effects of polyunsaturated fatty acids (PUFAs) on K(V)7 channel activity and possible underlying mechanisms of action. By summarizing reported effects of PUFAs on K(V)7 channels and native K(V)7-mediated currents, we conclude that the generally observed effect is a PUFA-induced increase in current amplitude. The increase in current is commonly associated with a shift in the voltage-dependence of channel opening and in some cases with increased maximum conductance. Auxiliary KCNE subunits, which associate with K(V)7 channels in certain tissues, may influence PUFA effects, though findings are conflicting. Both direct and indirect activating PUFA effects have been described, direct effects having been most extensively studied on K(V)7.1. The negative charge of the PUFA head-group has been identified as critical for electrostatic interaction with conserved positively charged amino acids in transmembrane segments 4 and 6. Additionally, the localization of double bonds in the PUFA tail tunes the apparent affinity of PUFAs to K(V)7.1. Indirect effects include those mediated by PUFA metabolites. Indirect inhibitory effects involve K(V)7 channel degradation and re-distribution from lipid rafts. Understanding how PUFAs regulate K(V)7 channels may provide insight into physiological regulation of K(V)7 channels and bring forth new therapeutic strategies. Frontiers Media S.A. 2020-06-11 /pmc/articles/PMC7300222/ /pubmed/32595524 http://dx.doi.org/10.3389/fphys.2020.00641 Text en Copyright © 2020 Larsson, Frampton and Liin. 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 Physiology
Larsson, Johan E.
Frampton, Damon J. A.
Liin, Sara I.
Polyunsaturated Fatty Acids as Modulators of K(V)7 Channels
title Polyunsaturated Fatty Acids as Modulators of K(V)7 Channels
title_full Polyunsaturated Fatty Acids as Modulators of K(V)7 Channels
title_fullStr Polyunsaturated Fatty Acids as Modulators of K(V)7 Channels
title_full_unstemmed Polyunsaturated Fatty Acids as Modulators of K(V)7 Channels
title_short Polyunsaturated Fatty Acids as Modulators of K(V)7 Channels
title_sort polyunsaturated fatty acids as modulators of k(v)7 channels
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300222/
https://www.ncbi.nlm.nih.gov/pubmed/32595524
http://dx.doi.org/10.3389/fphys.2020.00641
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