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Endothelial dysfunction in small arteries and early signs of atherosclerosis in ApoE knockout rats
Endothelial dysfunction is recognized as a major contributor to atherosclerosis and has been suggested to be evident far before plaque formation. Endothelial dysfunction in small resistance arteries has been suggested to initiate long before changes in conduit arteries. In this study, we address ear...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499202/ https://www.ncbi.nlm.nih.gov/pubmed/32943715 http://dx.doi.org/10.1038/s41598-020-72338-3 |
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author | Berenji Ardestani, Simin Eftedal, Ingrid Pedersen, Michael Jeppesen, Per Bendix Nørregaard, Rikke Matchkov, Vladimir V. |
author_facet | Berenji Ardestani, Simin Eftedal, Ingrid Pedersen, Michael Jeppesen, Per Bendix Nørregaard, Rikke Matchkov, Vladimir V. |
author_sort | Berenji Ardestani, Simin |
collection | PubMed |
description | Endothelial dysfunction is recognized as a major contributor to atherosclerosis and has been suggested to be evident far before plaque formation. Endothelial dysfunction in small resistance arteries has been suggested to initiate long before changes in conduit arteries. In this study, we address early changes in endothelial function of atherosclerosis prone rats. Male ApoE knockout (KO) rats (11- to 13-weeks-old) were subjected to either a Western or standard diet. The diet intervention continued for a period of 20–24 weeks. Endothelial function of pulmonary and mesenteric arteries was examined in vitro using an isometric myograph. We found that Western diet decreased the contribution of cyclooxygenase (COX) to control the vascular tone of both pulmonary and mesenteric arteries. These changes were associated with early stage atherosclerosis and elevated level of plasma total cholesterol, LDL and triglyceride in ApoE KO rats. Chondroid-transformed smooth muscle cells, calcifications, macrophages accumulation and foam cells were also observed in the aortic arch from ApoE KO rats fed Western diet. The ApoE KO rats are a new model to study endothelial dysfunction during the earlier stages of atherosclerosis and could help us improve preclinical drug development. |
format | Online Article Text |
id | pubmed-7499202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74992022020-09-22 Endothelial dysfunction in small arteries and early signs of atherosclerosis in ApoE knockout rats Berenji Ardestani, Simin Eftedal, Ingrid Pedersen, Michael Jeppesen, Per Bendix Nørregaard, Rikke Matchkov, Vladimir V. Sci Rep Article Endothelial dysfunction is recognized as a major contributor to atherosclerosis and has been suggested to be evident far before plaque formation. Endothelial dysfunction in small resistance arteries has been suggested to initiate long before changes in conduit arteries. In this study, we address early changes in endothelial function of atherosclerosis prone rats. Male ApoE knockout (KO) rats (11- to 13-weeks-old) were subjected to either a Western or standard diet. The diet intervention continued for a period of 20–24 weeks. Endothelial function of pulmonary and mesenteric arteries was examined in vitro using an isometric myograph. We found that Western diet decreased the contribution of cyclooxygenase (COX) to control the vascular tone of both pulmonary and mesenteric arteries. These changes were associated with early stage atherosclerosis and elevated level of plasma total cholesterol, LDL and triglyceride in ApoE KO rats. Chondroid-transformed smooth muscle cells, calcifications, macrophages accumulation and foam cells were also observed in the aortic arch from ApoE KO rats fed Western diet. The ApoE KO rats are a new model to study endothelial dysfunction during the earlier stages of atherosclerosis and could help us improve preclinical drug development. Nature Publishing Group UK 2020-09-17 /pmc/articles/PMC7499202/ /pubmed/32943715 http://dx.doi.org/10.1038/s41598-020-72338-3 Text en © The Author(s) 2020 Open AccessThis 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 Berenji Ardestani, Simin Eftedal, Ingrid Pedersen, Michael Jeppesen, Per Bendix Nørregaard, Rikke Matchkov, Vladimir V. Endothelial dysfunction in small arteries and early signs of atherosclerosis in ApoE knockout rats |
title | Endothelial dysfunction in small arteries and early signs of atherosclerosis in ApoE knockout rats |
title_full | Endothelial dysfunction in small arteries and early signs of atherosclerosis in ApoE knockout rats |
title_fullStr | Endothelial dysfunction in small arteries and early signs of atherosclerosis in ApoE knockout rats |
title_full_unstemmed | Endothelial dysfunction in small arteries and early signs of atherosclerosis in ApoE knockout rats |
title_short | Endothelial dysfunction in small arteries and early signs of atherosclerosis in ApoE knockout rats |
title_sort | endothelial dysfunction in small arteries and early signs of atherosclerosis in apoe knockout rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499202/ https://www.ncbi.nlm.nih.gov/pubmed/32943715 http://dx.doi.org/10.1038/s41598-020-72338-3 |
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