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Postranslational Modification of Ion Channels in Colonic Inflammation

Voltage-gated ion channels are key regulators of cell excitability. There is significant evidence that these channels are subject to modulation by redox status of the cells. Here we review the post-translational modifications of ion channels that occur in colonic inflammation. The redox mechanisms i...

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Detalles Bibliográficos
Autores principales: Akbarali, Hamid I., Kang, Minho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598435/
https://www.ncbi.nlm.nih.gov/pubmed/26411766
http://dx.doi.org/10.2174/1570159X13666150304001739
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author Akbarali, Hamid I.
Kang, Minho
author_facet Akbarali, Hamid I.
Kang, Minho
author_sort Akbarali, Hamid I.
collection PubMed
description Voltage-gated ion channels are key regulators of cell excitability. There is significant evidence that these channels are subject to modulation by redox status of the cells. Here we review the post-translational modifications of ion channels that occur in colonic inflammation. The redox mechanisms involve tyrosine nitration, covalent modification of cysteine residues and sulfhydration by hydrogen sulfide in experimental colitis. In the setting of colonic inflammation, modifications of cysteine and tyrosine are likely to occur at several sites within the same channel complex. In this review we describe alterations in channel function due to specific modifications of tyrosine and cysteine residues by reactive nitrogen, oxygen and hydrogen-sulfide resulting in altered motility.
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spelling pubmed-45984352015-10-13 Postranslational Modification of Ion Channels in Colonic Inflammation Akbarali, Hamid I. Kang, Minho Curr Neuropharmacol Article Voltage-gated ion channels are key regulators of cell excitability. There is significant evidence that these channels are subject to modulation by redox status of the cells. Here we review the post-translational modifications of ion channels that occur in colonic inflammation. The redox mechanisms involve tyrosine nitration, covalent modification of cysteine residues and sulfhydration by hydrogen sulfide in experimental colitis. In the setting of colonic inflammation, modifications of cysteine and tyrosine are likely to occur at several sites within the same channel complex. In this review we describe alterations in channel function due to specific modifications of tyrosine and cysteine residues by reactive nitrogen, oxygen and hydrogen-sulfide resulting in altered motility. Bentham Science Publishers 2015-03 2015-03 /pmc/articles/PMC4598435/ /pubmed/26411766 http://dx.doi.org/10.2174/1570159X13666150304001739 Text en ©2015 Bentham Science Publishers http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Akbarali, Hamid I.
Kang, Minho
Postranslational Modification of Ion Channels in Colonic Inflammation
title Postranslational Modification of Ion Channels in Colonic Inflammation
title_full Postranslational Modification of Ion Channels in Colonic Inflammation
title_fullStr Postranslational Modification of Ion Channels in Colonic Inflammation
title_full_unstemmed Postranslational Modification of Ion Channels in Colonic Inflammation
title_short Postranslational Modification of Ion Channels in Colonic Inflammation
title_sort postranslational modification of ion channels in colonic inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598435/
https://www.ncbi.nlm.nih.gov/pubmed/26411766
http://dx.doi.org/10.2174/1570159X13666150304001739
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