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Pharmacologic targeting of endothelial Ca(2+)-activated K(+) channels: A strategy to improve cardiovascular function
Endothelial small and intermediate-conductance, Ca(2+)-activated K(+) channels (KCa2.3 and KCa3.1, respectively) play an important role in the regulation of vascular function and systemic blood pressure. Growing evidence indicates that they are intimately involved in agonist-evoked vasodilation of s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972810/ https://www.ncbi.nlm.nih.gov/pubmed/29577810 http://dx.doi.org/10.1080/19336950.2018.1454814 |
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author | Mathew John, Cini Khaddaj Mallat, Rayan George, Grace Kim, Taeyeob Mishra, Ramesh C. Braun, Andrew P. |
author_facet | Mathew John, Cini Khaddaj Mallat, Rayan George, Grace Kim, Taeyeob Mishra, Ramesh C. Braun, Andrew P. |
author_sort | Mathew John, Cini |
collection | PubMed |
description | Endothelial small and intermediate-conductance, Ca(2+)-activated K(+) channels (KCa2.3 and KCa3.1, respectively) play an important role in the regulation of vascular function and systemic blood pressure. Growing evidence indicates that they are intimately involved in agonist-evoked vasodilation of small resistance arteries throughout the circulation. Small molecule activators of KCa2.x and 3.1 channels, such as SKA-31, can acutely inhibit myogenic tone in isolated resistance arteries, induce effective vasodilation in intact vascular beds, such as the coronary circulation, and acutely decrease systemic blood pressure in vivo. The blood pressure-lowering effect of SKA-31, and early indications of improvement in endothelial dysfunction suggest that endothelial KCa channel activators could eventually be developed into a new class of endothelial targeted agents to combat hypertension or atherosclerosis. This review summarises recent insights into the activation of endothelial Ca(2+) activated K(+) channels in various vascular beds, and how tools, such as SKA-31, may be beneficial in disease-related conditions. |
format | Online Article Text |
id | pubmed-5972810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-59728102018-05-31 Pharmacologic targeting of endothelial Ca(2+)-activated K(+) channels: A strategy to improve cardiovascular function Mathew John, Cini Khaddaj Mallat, Rayan George, Grace Kim, Taeyeob Mishra, Ramesh C. Braun, Andrew P. Channels (Austin) Review Endothelial small and intermediate-conductance, Ca(2+)-activated K(+) channels (KCa2.3 and KCa3.1, respectively) play an important role in the regulation of vascular function and systemic blood pressure. Growing evidence indicates that they are intimately involved in agonist-evoked vasodilation of small resistance arteries throughout the circulation. Small molecule activators of KCa2.x and 3.1 channels, such as SKA-31, can acutely inhibit myogenic tone in isolated resistance arteries, induce effective vasodilation in intact vascular beds, such as the coronary circulation, and acutely decrease systemic blood pressure in vivo. The blood pressure-lowering effect of SKA-31, and early indications of improvement in endothelial dysfunction suggest that endothelial KCa channel activators could eventually be developed into a new class of endothelial targeted agents to combat hypertension or atherosclerosis. This review summarises recent insights into the activation of endothelial Ca(2+) activated K(+) channels in various vascular beds, and how tools, such as SKA-31, may be beneficial in disease-related conditions. Taylor & Francis 2018-04-16 /pmc/articles/PMC5972810/ /pubmed/29577810 http://dx.doi.org/10.1080/19336950.2018.1454814 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Mathew John, Cini Khaddaj Mallat, Rayan George, Grace Kim, Taeyeob Mishra, Ramesh C. Braun, Andrew P. Pharmacologic targeting of endothelial Ca(2+)-activated K(+) channels: A strategy to improve cardiovascular function |
title | Pharmacologic targeting of endothelial Ca(2+)-activated K(+) channels: A strategy to improve cardiovascular function |
title_full | Pharmacologic targeting of endothelial Ca(2+)-activated K(+) channels: A strategy to improve cardiovascular function |
title_fullStr | Pharmacologic targeting of endothelial Ca(2+)-activated K(+) channels: A strategy to improve cardiovascular function |
title_full_unstemmed | Pharmacologic targeting of endothelial Ca(2+)-activated K(+) channels: A strategy to improve cardiovascular function |
title_short | Pharmacologic targeting of endothelial Ca(2+)-activated K(+) channels: A strategy to improve cardiovascular function |
title_sort | pharmacologic targeting of endothelial ca(2+)-activated k(+) channels: a strategy to improve cardiovascular function |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5972810/ https://www.ncbi.nlm.nih.gov/pubmed/29577810 http://dx.doi.org/10.1080/19336950.2018.1454814 |
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