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Impact of Short-Term Treatment with Telmisartan on Cerebral Arterial Remodeling in SHR
BACKGROUND AND PURPOSE: Chronic hypertension decreases internal diameter of cerebral arteries and arterioles. We recently showed that short-term treatment with the angiotensin II receptor blocker telmisartan restored baseline internal diameter of small cerebral arterioles in spontaneously hypertensi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198293/ https://www.ncbi.nlm.nih.gov/pubmed/25333878 http://dx.doi.org/10.1371/journal.pone.0110766 |
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author | Foulquier, Sébastien Lartaud, Isabelle Dupuis, François |
author_facet | Foulquier, Sébastien Lartaud, Isabelle Dupuis, François |
author_sort | Foulquier, Sébastien |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Chronic hypertension decreases internal diameter of cerebral arteries and arterioles. We recently showed that short-term treatment with the angiotensin II receptor blocker telmisartan restored baseline internal diameter of small cerebral arterioles in spontaneously hypertensive rats (SHR), via reversal of structural remodeling and inhibition of the angiotensin II vasoconstrictor response. As larger arteries also participate in the regulation of cerebral circulation, we evaluated whether similar short-term treatment affects middle cerebral arteries of SHR. METHODS: Baseline internal diameters of pressurised middle cerebral arteries from SHR and their respective controls, Wistar Kyoto rats (WKY) and responses to angiotensin II were studied in a small vessel arteriograph. Pressure myogenic curves and passive internal diameters were measured following EDTA deactivation, and elastic modulus from stress-strain relationships. RESULTS: Active baseline internal diameter was 23% lower in SHR compared to WKY, passive internal diameter (EDTA) 28% lower and elastic modulus unchanged. Pressure myogenic curves were shifted to higher pressure values in SHR. Telmisartan lowered blood pressure but had no effect on baseline internal diameter nor on structural remodeling (passive internal diameter and elastic modulus remained unchanged compared to SHR). Telmisartan shifted the pressure myogenic curve to lower pressure values than SHR. CONCLUSION: In the middle cerebral arteries of SHR, short-term treatment with telmisartan had no effect on structural remodeling and did not restore baseline internal diameter, but allowed myogenic tone to adapt towards lower pressure values. |
format | Online Article Text |
id | pubmed-4198293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41982932014-10-21 Impact of Short-Term Treatment with Telmisartan on Cerebral Arterial Remodeling in SHR Foulquier, Sébastien Lartaud, Isabelle Dupuis, François PLoS One Research Article BACKGROUND AND PURPOSE: Chronic hypertension decreases internal diameter of cerebral arteries and arterioles. We recently showed that short-term treatment with the angiotensin II receptor blocker telmisartan restored baseline internal diameter of small cerebral arterioles in spontaneously hypertensive rats (SHR), via reversal of structural remodeling and inhibition of the angiotensin II vasoconstrictor response. As larger arteries also participate in the regulation of cerebral circulation, we evaluated whether similar short-term treatment affects middle cerebral arteries of SHR. METHODS: Baseline internal diameters of pressurised middle cerebral arteries from SHR and their respective controls, Wistar Kyoto rats (WKY) and responses to angiotensin II were studied in a small vessel arteriograph. Pressure myogenic curves and passive internal diameters were measured following EDTA deactivation, and elastic modulus from stress-strain relationships. RESULTS: Active baseline internal diameter was 23% lower in SHR compared to WKY, passive internal diameter (EDTA) 28% lower and elastic modulus unchanged. Pressure myogenic curves were shifted to higher pressure values in SHR. Telmisartan lowered blood pressure but had no effect on baseline internal diameter nor on structural remodeling (passive internal diameter and elastic modulus remained unchanged compared to SHR). Telmisartan shifted the pressure myogenic curve to lower pressure values than SHR. CONCLUSION: In the middle cerebral arteries of SHR, short-term treatment with telmisartan had no effect on structural remodeling and did not restore baseline internal diameter, but allowed myogenic tone to adapt towards lower pressure values. Public Library of Science 2014-10-15 /pmc/articles/PMC4198293/ /pubmed/25333878 http://dx.doi.org/10.1371/journal.pone.0110766 Text en © 2014 Foulquier et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Foulquier, Sébastien Lartaud, Isabelle Dupuis, François Impact of Short-Term Treatment with Telmisartan on Cerebral Arterial Remodeling in SHR |
title | Impact of Short-Term Treatment with Telmisartan on Cerebral Arterial Remodeling in SHR |
title_full | Impact of Short-Term Treatment with Telmisartan on Cerebral Arterial Remodeling in SHR |
title_fullStr | Impact of Short-Term Treatment with Telmisartan on Cerebral Arterial Remodeling in SHR |
title_full_unstemmed | Impact of Short-Term Treatment with Telmisartan on Cerebral Arterial Remodeling in SHR |
title_short | Impact of Short-Term Treatment with Telmisartan on Cerebral Arterial Remodeling in SHR |
title_sort | impact of short-term treatment with telmisartan on cerebral arterial remodeling in shr |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198293/ https://www.ncbi.nlm.nih.gov/pubmed/25333878 http://dx.doi.org/10.1371/journal.pone.0110766 |
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