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Age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels

Age and hypertension are major causes of large artery remodeling and stiffening, a cardiovascular risk factor for heart and kidney damage. The aged spontaneously hypertensive rat (SHR) model is recognized for human cardiovascular pathology, but discrepancies appeared in studies of arterial stiffness...

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Autores principales: Lindesay, George, Ragonnet, Christophe, Chimenti, Stefano, Villeneuve, Nicole, Vayssettes‐Courchay, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886171/
https://www.ncbi.nlm.nih.gov/pubmed/27233301
http://dx.doi.org/10.14814/phy2.12805
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author Lindesay, George
Ragonnet, Christophe
Chimenti, Stefano
Villeneuve, Nicole
Vayssettes‐Courchay, Christine
author_facet Lindesay, George
Ragonnet, Christophe
Chimenti, Stefano
Villeneuve, Nicole
Vayssettes‐Courchay, Christine
author_sort Lindesay, George
collection PubMed
description Age and hypertension are major causes of large artery remodeling and stiffening, a cardiovascular risk factor for heart and kidney damage. The aged spontaneously hypertensive rat (SHR) model is recognized for human cardiovascular pathology, but discrepancies appeared in studies of arterial stiffness. We performed experiments using a robust analysis via echo tracking in 20‐week adult (n = 8) and 80‐week‐old SHR (n = 7), with age‐matched normotensive Wistar Kyoto rats (WKY, n = 6;6) at basal and matched levels of blood pressure (BP). After anesthesia with pentobarbital, abdominal aortic diameter and pressure were recorded and BP was decreased by clonidine i.v. At basal BP, aortic pulse distension, compliance, and distensibility (AD) were reduced and stiffness index increased with age and hypertension and further altered with age + hypertension. When BP was adjusted in SHR to that of normotensive rats (130 mmHg), there was no difference between 20‐week‐old SHR and WKY. Importantly, the age effect was maintained in both WKY and SHR and accentuated by hypertension in old rats. At 130 mmHg, with similar pulse pressure in the four groups, AD (kPa(−3)) = 24.2 ± 1 in 20 weeks WKY, 19.7 ± 1.4 in 20 weeks SHR, 12.4 ± 1.3 in 80 weeks WKY and 6.6 ± 0.6 in 80 weeks SHR; distension = 7.6 ± 0.4%, 6.7 ± 0.6%, 3.7 ± 0.3%, and 1.8 ± 0.2% in the same groups. In conclusion, reduced distensibility, that is, stiffening due to age is clearly shown here in both WKY and SHR as well as a synergistic effect of age and hypertension. This technique will allow new studies on the mechanisms responsible and drug intervention.
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spelling pubmed-48861712016-08-17 Age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels Lindesay, George Ragonnet, Christophe Chimenti, Stefano Villeneuve, Nicole Vayssettes‐Courchay, Christine Physiol Rep Original Research Age and hypertension are major causes of large artery remodeling and stiffening, a cardiovascular risk factor for heart and kidney damage. The aged spontaneously hypertensive rat (SHR) model is recognized for human cardiovascular pathology, but discrepancies appeared in studies of arterial stiffness. We performed experiments using a robust analysis via echo tracking in 20‐week adult (n = 8) and 80‐week‐old SHR (n = 7), with age‐matched normotensive Wistar Kyoto rats (WKY, n = 6;6) at basal and matched levels of blood pressure (BP). After anesthesia with pentobarbital, abdominal aortic diameter and pressure were recorded and BP was decreased by clonidine i.v. At basal BP, aortic pulse distension, compliance, and distensibility (AD) were reduced and stiffness index increased with age and hypertension and further altered with age + hypertension. When BP was adjusted in SHR to that of normotensive rats (130 mmHg), there was no difference between 20‐week‐old SHR and WKY. Importantly, the age effect was maintained in both WKY and SHR and accentuated by hypertension in old rats. At 130 mmHg, with similar pulse pressure in the four groups, AD (kPa(−3)) = 24.2 ± 1 in 20 weeks WKY, 19.7 ± 1.4 in 20 weeks SHR, 12.4 ± 1.3 in 80 weeks WKY and 6.6 ± 0.6 in 80 weeks SHR; distension = 7.6 ± 0.4%, 6.7 ± 0.6%, 3.7 ± 0.3%, and 1.8 ± 0.2% in the same groups. In conclusion, reduced distensibility, that is, stiffening due to age is clearly shown here in both WKY and SHR as well as a synergistic effect of age and hypertension. This technique will allow new studies on the mechanisms responsible and drug intervention. John Wiley and Sons Inc. 2016-05-27 /pmc/articles/PMC4886171/ /pubmed/27233301 http://dx.doi.org/10.14814/phy2.12805 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Lindesay, George
Ragonnet, Christophe
Chimenti, Stefano
Villeneuve, Nicole
Vayssettes‐Courchay, Christine
Age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels
title Age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels
title_full Age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels
title_fullStr Age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels
title_full_unstemmed Age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels
title_short Age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels
title_sort age and hypertension strongly induce aortic stiffening in rats at basal and matched blood pressure levels
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886171/
https://www.ncbi.nlm.nih.gov/pubmed/27233301
http://dx.doi.org/10.14814/phy2.12805
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