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Vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model

Vascular calcification is a risk factor for cardiovascular and kidney diseases. Medial calcification may differently affect the arterial tree depending on vessel location and smooth muscle injury. The aim was to map the anatomical distribution of vascular calcifications on different arteries and art...

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Autores principales: Muyor, Karen, Laget, Jonas, Cortijo, Irene, Duranton, Flore, Jover, Bernard, Argilés, Àngel, Gayrard, Nathalie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279329/
https://www.ncbi.nlm.nih.gov/pubmed/35831341
http://dx.doi.org/10.1038/s41598-022-15739-w
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author Muyor, Karen
Laget, Jonas
Cortijo, Irene
Duranton, Flore
Jover, Bernard
Argilés, Àngel
Gayrard, Nathalie
author_facet Muyor, Karen
Laget, Jonas
Cortijo, Irene
Duranton, Flore
Jover, Bernard
Argilés, Àngel
Gayrard, Nathalie
author_sort Muyor, Karen
collection PubMed
description Vascular calcification is a risk factor for cardiovascular and kidney diseases. Medial calcification may differently affect the arterial tree depending on vessel location and smooth muscle injury. The aim was to map the anatomical distribution of vascular calcifications on different arteries and artery locations, in cultured artery rings (ex vivo) and in a rat model of elastocalcinosis (in vivo). Vascular calcification was assessed histologically (von Kossa staining of the media) and by calcium content measurement. Arteries of different sizes were harvested from untreated rats for ring culture and from the vitamin D(3)-nicotine (VDN) rat model for direct observation. When cultured in pro-calcifying conditions, thoracic aorta exhibited similar calcification from the arch to the diaphragm. Calcification increased in abdominal aorta along with the reduction in cross sectional area. Carotid and renal arteries exhibited similar ex vivo calcification. In VDN rats, calcification was greater in carotid artery than in aorta, and was accompanied by fibrosis and apoptosis. Ex vivo, calcification was increased by the induction of lesions on arteries. Along the vascular tree, calcification of the arterial wall increases with the narrowing of vessels in ex vivo ring culture and in vivo. The observed differences represent local susceptibility of the vessels to the calcifying processes.
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spelling pubmed-92793292022-07-15 Vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model Muyor, Karen Laget, Jonas Cortijo, Irene Duranton, Flore Jover, Bernard Argilés, Àngel Gayrard, Nathalie Sci Rep Article Vascular calcification is a risk factor for cardiovascular and kidney diseases. Medial calcification may differently affect the arterial tree depending on vessel location and smooth muscle injury. The aim was to map the anatomical distribution of vascular calcifications on different arteries and artery locations, in cultured artery rings (ex vivo) and in a rat model of elastocalcinosis (in vivo). Vascular calcification was assessed histologically (von Kossa staining of the media) and by calcium content measurement. Arteries of different sizes were harvested from untreated rats for ring culture and from the vitamin D(3)-nicotine (VDN) rat model for direct observation. When cultured in pro-calcifying conditions, thoracic aorta exhibited similar calcification from the arch to the diaphragm. Calcification increased in abdominal aorta along with the reduction in cross sectional area. Carotid and renal arteries exhibited similar ex vivo calcification. In VDN rats, calcification was greater in carotid artery than in aorta, and was accompanied by fibrosis and apoptosis. Ex vivo, calcification was increased by the induction of lesions on arteries. Along the vascular tree, calcification of the arterial wall increases with the narrowing of vessels in ex vivo ring culture and in vivo. The observed differences represent local susceptibility of the vessels to the calcifying processes. Nature Publishing Group UK 2022-07-13 /pmc/articles/PMC9279329/ /pubmed/35831341 http://dx.doi.org/10.1038/s41598-022-15739-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Muyor, Karen
Laget, Jonas
Cortijo, Irene
Duranton, Flore
Jover, Bernard
Argilés, Àngel
Gayrard, Nathalie
Vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model
title Vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model
title_full Vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model
title_fullStr Vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model
title_full_unstemmed Vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model
title_short Vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model
title_sort vascular calcification in different arterial beds in ex vivo ring culture and in vivo rat model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9279329/
https://www.ncbi.nlm.nih.gov/pubmed/35831341
http://dx.doi.org/10.1038/s41598-022-15739-w
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