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Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion

Obstructive sleep apnea syndrome (OSA) promotes aortic dilatation, increased stiffness and accelerated atherosclerosis, but the mechanisms of vascular remodelling are not known. We aimed to assess vascular remodelling, its mechanisms, and the effect of mesenchymal stem cells (MSC) infusions in a cli...

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Autores principales: Rubies, Cira, Dantas, Ana-Paula, Batlle, Montserrat, Torres, Marta, Farre, Ramon, Sangüesa, Gemma, Montserrat, Josep M., Mont, Lluis, Almendros, Isaac, Guasch, Eduard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685984/
https://www.ncbi.nlm.nih.gov/pubmed/31391506
http://dx.doi.org/10.1038/s41598-019-47813-1
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author Rubies, Cira
Dantas, Ana-Paula
Batlle, Montserrat
Torres, Marta
Farre, Ramon
Sangüesa, Gemma
Montserrat, Josep M.
Mont, Lluis
Almendros, Isaac
Guasch, Eduard
author_facet Rubies, Cira
Dantas, Ana-Paula
Batlle, Montserrat
Torres, Marta
Farre, Ramon
Sangüesa, Gemma
Montserrat, Josep M.
Mont, Lluis
Almendros, Isaac
Guasch, Eduard
author_sort Rubies, Cira
collection PubMed
description Obstructive sleep apnea syndrome (OSA) promotes aortic dilatation, increased stiffness and accelerated atherosclerosis, but the mechanisms of vascular remodelling are not known. We aimed to assess vascular remodelling, its mechanisms, and the effect of mesenchymal stem cells (MSC) infusions in a clinically relevant rat model of chronic OSA involving recurrent airway obstructions leading thoracic pressure swings and intermittent hypoxia/hypercapnia (OSA-rats). Another group of rats were placed in the same setup without air obstructions (Sham-rats) and were considered controls. Our study demonstrates that chronic, non-invasive repetitive airway obstructions mimicking OSA promote remarkable structural changes of the descending thoracic aorta such as eccentric aortic hypertrophy due to an increased wall thickness and lumen diameter, an increase in the number of elastin fibers which, in contrast, get ruptured, but no changes in tunica media fibrosis. As putative molecular mechanisms of the OSA-induced vascular changes we identified an increase in reactive oxygen species and renin-angiotensin system markers and an imbalance in oxide nitric synthesis. Our results also indicate that MSC infusion blunts the OSA-related vascular changes, most probably due to their anti-inflammatory properties.
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spelling pubmed-66859842019-08-12 Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion Rubies, Cira Dantas, Ana-Paula Batlle, Montserrat Torres, Marta Farre, Ramon Sangüesa, Gemma Montserrat, Josep M. Mont, Lluis Almendros, Isaac Guasch, Eduard Sci Rep Article Obstructive sleep apnea syndrome (OSA) promotes aortic dilatation, increased stiffness and accelerated atherosclerosis, but the mechanisms of vascular remodelling are not known. We aimed to assess vascular remodelling, its mechanisms, and the effect of mesenchymal stem cells (MSC) infusions in a clinically relevant rat model of chronic OSA involving recurrent airway obstructions leading thoracic pressure swings and intermittent hypoxia/hypercapnia (OSA-rats). Another group of rats were placed in the same setup without air obstructions (Sham-rats) and were considered controls. Our study demonstrates that chronic, non-invasive repetitive airway obstructions mimicking OSA promote remarkable structural changes of the descending thoracic aorta such as eccentric aortic hypertrophy due to an increased wall thickness and lumen diameter, an increase in the number of elastin fibers which, in contrast, get ruptured, but no changes in tunica media fibrosis. As putative molecular mechanisms of the OSA-induced vascular changes we identified an increase in reactive oxygen species and renin-angiotensin system markers and an imbalance in oxide nitric synthesis. Our results also indicate that MSC infusion blunts the OSA-related vascular changes, most probably due to their anti-inflammatory properties. Nature Publishing Group UK 2019-08-07 /pmc/articles/PMC6685984/ /pubmed/31391506 http://dx.doi.org/10.1038/s41598-019-47813-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rubies, Cira
Dantas, Ana-Paula
Batlle, Montserrat
Torres, Marta
Farre, Ramon
Sangüesa, Gemma
Montserrat, Josep M.
Mont, Lluis
Almendros, Isaac
Guasch, Eduard
Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion
title Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion
title_full Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion
title_fullStr Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion
title_full_unstemmed Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion
title_short Aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion
title_sort aortic remodelling induced by obstructive apneas is normalized with mesenchymal stem cells infusion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685984/
https://www.ncbi.nlm.nih.gov/pubmed/31391506
http://dx.doi.org/10.1038/s41598-019-47813-1
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