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Pathophysiology of the atherosclerotic rabbit.

The pathophysiology and histopathology caused by feeding rabbits a diet containing 2% cholesterol is described. Cholesterol deposition was seen in almost all organs after 15 weeks on the diet. Lesions were seen as early as 7 weeks in the aorta and pulmonary vessels and by 11 weeks in the small intra...

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Detalles Bibliográficos
Autores principales: Lee, R J, Zaidi, I H, Baky, S H
Formato: Texto
Lenguaje:English
Publicado: 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637257/
https://www.ncbi.nlm.nih.gov/pubmed/720316
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author Lee, R J
Zaidi, I H
Baky, S H
author_facet Lee, R J
Zaidi, I H
Baky, S H
author_sort Lee, R J
collection PubMed
description The pathophysiology and histopathology caused by feeding rabbits a diet containing 2% cholesterol is described. Cholesterol deposition was seen in almost all organs after 15 weeks on the diet. Lesions were seen as early as 7 weeks in the aorta and pulmonary vessels and by 11 weeks in the small intramyocardial arteries and arterioles. Evidence of myocardial ischemia could be elicited by stressing the heart by electrical pacing at rapid rates or by administration of pharmacological agents which increased oxygen consumption (isoproterenol) or decreased oxygen supply (ergonovine). Susceptibility to such stress was increased by isovolumic hemodilution which decreased the oxygen-carrying capacity of the blood. Myocardial fibrosis and infarction were evident by 15 weeks on the diet and cardiac reserve was depleted by 25 weeks as evidenced by the presence of ascites in all animals examined. The preliminary results reported here suggest that further evaluation of the atherosclerotic rabbit as a cardiac toxicity model is warranted.
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spelling pubmed-16372572006-11-17 Pathophysiology of the atherosclerotic rabbit. Lee, R J Zaidi, I H Baky, S H Environ Health Perspect Research Article The pathophysiology and histopathology caused by feeding rabbits a diet containing 2% cholesterol is described. Cholesterol deposition was seen in almost all organs after 15 weeks on the diet. Lesions were seen as early as 7 weeks in the aorta and pulmonary vessels and by 11 weeks in the small intramyocardial arteries and arterioles. Evidence of myocardial ischemia could be elicited by stressing the heart by electrical pacing at rapid rates or by administration of pharmacological agents which increased oxygen consumption (isoproterenol) or decreased oxygen supply (ergonovine). Susceptibility to such stress was increased by isovolumic hemodilution which decreased the oxygen-carrying capacity of the blood. Myocardial fibrosis and infarction were evident by 15 weeks on the diet and cardiac reserve was depleted by 25 weeks as evidenced by the presence of ascites in all animals examined. The preliminary results reported here suggest that further evaluation of the atherosclerotic rabbit as a cardiac toxicity model is warranted. 1978-10 /pmc/articles/PMC1637257/ /pubmed/720316 Text en
spellingShingle Research Article
Lee, R J
Zaidi, I H
Baky, S H
Pathophysiology of the atherosclerotic rabbit.
title Pathophysiology of the atherosclerotic rabbit.
title_full Pathophysiology of the atherosclerotic rabbit.
title_fullStr Pathophysiology of the atherosclerotic rabbit.
title_full_unstemmed Pathophysiology of the atherosclerotic rabbit.
title_short Pathophysiology of the atherosclerotic rabbit.
title_sort pathophysiology of the atherosclerotic rabbit.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637257/
https://www.ncbi.nlm.nih.gov/pubmed/720316
work_keys_str_mv AT leerj pathophysiologyoftheatheroscleroticrabbit
AT zaidiih pathophysiologyoftheatheroscleroticrabbit
AT bakysh pathophysiologyoftheatheroscleroticrabbit