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Cardiac and vascular phenotypes in the apolipoprotein E-deficient mouse
Cardiovascular death is frequently associated with atherosclerosis, a chronic multifactorial disease and a leading cause of death worldwide. Genetically engineered mouse models have proven useful for the study of the mechanisms underlying cardiovascular diseases. The apolipoprotein E-deficient mouse...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306747/ https://www.ncbi.nlm.nih.gov/pubmed/22330242 http://dx.doi.org/10.1186/1423-0127-19-22 |
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author | Vasquez, Elisardo C Peotta, Veronica A Gava, Agata L Pereira, Thiago MC Meyrelles, Silvana S |
author_facet | Vasquez, Elisardo C Peotta, Veronica A Gava, Agata L Pereira, Thiago MC Meyrelles, Silvana S |
author_sort | Vasquez, Elisardo C |
collection | PubMed |
description | Cardiovascular death is frequently associated with atherosclerosis, a chronic multifactorial disease and a leading cause of death worldwide. Genetically engineered mouse models have proven useful for the study of the mechanisms underlying cardiovascular diseases. The apolipoprotein E-deficient mouse has been the most widely used animal model of atherosclerosis because it rapidly develops severe hypercholesterolemia and spontaneous atherosclerotic lesions similar to those observed in humans. In this review, we provide an overview of the cardiac and vascular phenotypes and discuss the interplay among nitric oxide, reactive oxygen species, aging and diet in the impairment of cardiovascular function in this mouse model. |
format | Online Article Text |
id | pubmed-3306747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33067472012-03-18 Cardiac and vascular phenotypes in the apolipoprotein E-deficient mouse Vasquez, Elisardo C Peotta, Veronica A Gava, Agata L Pereira, Thiago MC Meyrelles, Silvana S J Biomed Sci Review Cardiovascular death is frequently associated with atherosclerosis, a chronic multifactorial disease and a leading cause of death worldwide. Genetically engineered mouse models have proven useful for the study of the mechanisms underlying cardiovascular diseases. The apolipoprotein E-deficient mouse has been the most widely used animal model of atherosclerosis because it rapidly develops severe hypercholesterolemia and spontaneous atherosclerotic lesions similar to those observed in humans. In this review, we provide an overview of the cardiac and vascular phenotypes and discuss the interplay among nitric oxide, reactive oxygen species, aging and diet in the impairment of cardiovascular function in this mouse model. BioMed Central 2012-02-13 /pmc/articles/PMC3306747/ /pubmed/22330242 http://dx.doi.org/10.1186/1423-0127-19-22 Text en Copyright ©2012 Vasquez et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Vasquez, Elisardo C Peotta, Veronica A Gava, Agata L Pereira, Thiago MC Meyrelles, Silvana S Cardiac and vascular phenotypes in the apolipoprotein E-deficient mouse |
title | Cardiac and vascular phenotypes in the apolipoprotein E-deficient mouse |
title_full | Cardiac and vascular phenotypes in the apolipoprotein E-deficient mouse |
title_fullStr | Cardiac and vascular phenotypes in the apolipoprotein E-deficient mouse |
title_full_unstemmed | Cardiac and vascular phenotypes in the apolipoprotein E-deficient mouse |
title_short | Cardiac and vascular phenotypes in the apolipoprotein E-deficient mouse |
title_sort | cardiac and vascular phenotypes in the apolipoprotein e-deficient mouse |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3306747/ https://www.ncbi.nlm.nih.gov/pubmed/22330242 http://dx.doi.org/10.1186/1423-0127-19-22 |
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