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Efficacy of Female Rat Models in Translational Cardiovascular Aging Research

Cardiovascular disease is the leading cause of death in women in the United States. Aging is a primary risk factor for the development of cardiovascular disease as well as cardiovascular-related morbidity and mortality. Aging is a universal process that all humans undergo; however, research in aging...

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Detalles Bibliográficos
Autores principales: Rice, K. M., Fannin, J. C., Gillette, C., Blough, E. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294461/
https://www.ncbi.nlm.nih.gov/pubmed/25610649
http://dx.doi.org/10.1155/2014/153127
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author Rice, K. M.
Fannin, J. C.
Gillette, C.
Blough, E. R.
author_facet Rice, K. M.
Fannin, J. C.
Gillette, C.
Blough, E. R.
author_sort Rice, K. M.
collection PubMed
description Cardiovascular disease is the leading cause of death in women in the United States. Aging is a primary risk factor for the development of cardiovascular disease as well as cardiovascular-related morbidity and mortality. Aging is a universal process that all humans undergo; however, research in aging is limited by cost and time constraints. Therefore, most research in aging has been done in primates and rodents; however it is unknown how well the effects of aging in rat models translate into humans. To compound the complication of aging gender has also been indicated as a risk factor for various cardiovascular diseases. This review addresses the systemic pathophysiology of the cardiovascular system associated with aging and gender for aging research with regard to the applicability of rat derived data for translational application to human aging.
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spelling pubmed-42944612015-01-21 Efficacy of Female Rat Models in Translational Cardiovascular Aging Research Rice, K. M. Fannin, J. C. Gillette, C. Blough, E. R. J Aging Res Review Article Cardiovascular disease is the leading cause of death in women in the United States. Aging is a primary risk factor for the development of cardiovascular disease as well as cardiovascular-related morbidity and mortality. Aging is a universal process that all humans undergo; however, research in aging is limited by cost and time constraints. Therefore, most research in aging has been done in primates and rodents; however it is unknown how well the effects of aging in rat models translate into humans. To compound the complication of aging gender has also been indicated as a risk factor for various cardiovascular diseases. This review addresses the systemic pathophysiology of the cardiovascular system associated with aging and gender for aging research with regard to the applicability of rat derived data for translational application to human aging. Hindawi Publishing Corporation 2014 2014-12-31 /pmc/articles/PMC4294461/ /pubmed/25610649 http://dx.doi.org/10.1155/2014/153127 Text en Copyright © 2014 K. M. Rice et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Rice, K. M.
Fannin, J. C.
Gillette, C.
Blough, E. R.
Efficacy of Female Rat Models in Translational Cardiovascular Aging Research
title Efficacy of Female Rat Models in Translational Cardiovascular Aging Research
title_full Efficacy of Female Rat Models in Translational Cardiovascular Aging Research
title_fullStr Efficacy of Female Rat Models in Translational Cardiovascular Aging Research
title_full_unstemmed Efficacy of Female Rat Models in Translational Cardiovascular Aging Research
title_short Efficacy of Female Rat Models in Translational Cardiovascular Aging Research
title_sort efficacy of female rat models in translational cardiovascular aging research
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294461/
https://www.ncbi.nlm.nih.gov/pubmed/25610649
http://dx.doi.org/10.1155/2014/153127
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