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Closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach
Block of voltage-gated potassium (Kv) channels has been demonstrated to affect neuronal activity described as increasing excitability. The effect has been associated with a closed-state dependent block. However, the block of Kv channels in e.g. local anesthetic and antiarrhythmics, is open state-dep...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546692/ https://www.ncbi.nlm.nih.gov/pubmed/31160624 http://dx.doi.org/10.1038/s41598-019-44564-x |
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author | Ågren, Richard Nilsson, Johanna Århem, Peter |
author_facet | Ågren, Richard Nilsson, Johanna Århem, Peter |
author_sort | Ågren, Richard |
collection | PubMed |
description | Block of voltage-gated potassium (Kv) channels has been demonstrated to affect neuronal activity described as increasing excitability. The effect has been associated with a closed-state dependent block. However, the block of Kv channels in e.g. local anesthetic and antiarrhythmics, is open state-dependent. Since the reduced excitability in this case mainly is due to sodium channel block, the role of the Kv channel block is concealed. The present investigation aims to analyse the specific role of state-dependent Kv channel block for excitability. Using a computational approach, with introduced blocked states in the Kv channel of the Frankenhaeuser-Huxley axon membrane model, we calculated the effects on threshold, firing and presynaptic Ca influx. The Ca influx was obtained from an N-type Cav channel model linked to the Frankenhaeuser-Huxley membrane. The results suggested that a selective block of open Kv channels decreased the rate of repetitive firing and the consequent Ca influx, thus challenging the traditional view. In contrast, presence of a closed-state block, increased the firing rate and the Ca influx. These findings propose that Kv channel block may either increase or decrease cellular excitability, thus highlighting the importance of further investigating the role of state-specific blocking mechanisms. |
format | Online Article Text |
id | pubmed-6546692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65466922019-06-10 Closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach Ågren, Richard Nilsson, Johanna Århem, Peter Sci Rep Article Block of voltage-gated potassium (Kv) channels has been demonstrated to affect neuronal activity described as increasing excitability. The effect has been associated with a closed-state dependent block. However, the block of Kv channels in e.g. local anesthetic and antiarrhythmics, is open state-dependent. Since the reduced excitability in this case mainly is due to sodium channel block, the role of the Kv channel block is concealed. The present investigation aims to analyse the specific role of state-dependent Kv channel block for excitability. Using a computational approach, with introduced blocked states in the Kv channel of the Frankenhaeuser-Huxley axon membrane model, we calculated the effects on threshold, firing and presynaptic Ca influx. The Ca influx was obtained from an N-type Cav channel model linked to the Frankenhaeuser-Huxley membrane. The results suggested that a selective block of open Kv channels decreased the rate of repetitive firing and the consequent Ca influx, thus challenging the traditional view. In contrast, presence of a closed-state block, increased the firing rate and the Ca influx. These findings propose that Kv channel block may either increase or decrease cellular excitability, thus highlighting the importance of further investigating the role of state-specific blocking mechanisms. Nature Publishing Group UK 2019-06-03 /pmc/articles/PMC6546692/ /pubmed/31160624 http://dx.doi.org/10.1038/s41598-019-44564-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ågren, Richard Nilsson, Johanna Århem, Peter Closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach |
title | Closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach |
title_full | Closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach |
title_fullStr | Closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach |
title_full_unstemmed | Closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach |
title_short | Closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach |
title_sort | closed and open state dependent block of potassium channels cause opposing effects on excitability – a computational approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546692/ https://www.ncbi.nlm.nih.gov/pubmed/31160624 http://dx.doi.org/10.1038/s41598-019-44564-x |
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