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Kv7 and Kv11 channels in myometrial regulation
Ion channels play a key role in defining myometrial contractility. Modulation of ion channel populations is proposed to underpin gestational changes in uterine contractility associated with the transition from uterine quiescence to active labour. Of the myriad ion channels present in the uterus, thi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165302/ https://www.ncbi.nlm.nih.gov/pubmed/24121285 http://dx.doi.org/10.1113/expphysiol.2013.075754 |
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author | Greenwood, Iain A Tribe, Rachel M |
author_facet | Greenwood, Iain A Tribe, Rachel M |
author_sort | Greenwood, Iain A |
collection | PubMed |
description | Ion channels play a key role in defining myometrial contractility. Modulation of ion channel populations is proposed to underpin gestational changes in uterine contractility associated with the transition from uterine quiescence to active labour. Of the myriad ion channels present in the uterus, this article will focus upon potassium channels encoded by the KCNQ genes and ether-à-go-go-related (ERG) genes. Voltage-gated potassium channels encoded by KCNQ and ERG (termed Kv7 and Kv11, respectively) are accepted as major determinants of neuronal excitability and the duration of the cardiac action potential. However, there is now growing appreciation that these ion channels have a major functional impact in vascular and non-vascular smooth muscle. Moreover, Kv7 channels may be potential therapeutic targets for the treatment of preterm labour. |
format | Online Article Text |
id | pubmed-4165302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41653022014-10-08 Kv7 and Kv11 channels in myometrial regulation Greenwood, Iain A Tribe, Rachel M Exp Physiol Symposium Reports Ion channels play a key role in defining myometrial contractility. Modulation of ion channel populations is proposed to underpin gestational changes in uterine contractility associated with the transition from uterine quiescence to active labour. Of the myriad ion channels present in the uterus, this article will focus upon potassium channels encoded by the KCNQ genes and ether-à-go-go-related (ERG) genes. Voltage-gated potassium channels encoded by KCNQ and ERG (termed Kv7 and Kv11, respectively) are accepted as major determinants of neuronal excitability and the duration of the cardiac action potential. However, there is now growing appreciation that these ion channels have a major functional impact in vascular and non-vascular smooth muscle. Moreover, Kv7 channels may be potential therapeutic targets for the treatment of preterm labour. Blackwell Publishing Ltd 2014-03-01 2013-10-11 /pmc/articles/PMC4165302/ /pubmed/24121285 http://dx.doi.org/10.1113/expphysiol.2013.075754 Text en © 2013 The Authors. Experimental Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Symposium Reports Greenwood, Iain A Tribe, Rachel M Kv7 and Kv11 channels in myometrial regulation |
title | Kv7 and Kv11 channels in myometrial regulation |
title_full | Kv7 and Kv11 channels in myometrial regulation |
title_fullStr | Kv7 and Kv11 channels in myometrial regulation |
title_full_unstemmed | Kv7 and Kv11 channels in myometrial regulation |
title_short | Kv7 and Kv11 channels in myometrial regulation |
title_sort | kv7 and kv11 channels in myometrial regulation |
topic | Symposium Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165302/ https://www.ncbi.nlm.nih.gov/pubmed/24121285 http://dx.doi.org/10.1113/expphysiol.2013.075754 |
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