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Developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury

BACKGROUND: It is widely believed that atherosclerotic plaque rupture and subsequent thrombosis leads to acute coronary events and stroke. However, study of the mechanism and treatment of human plaque rupture is hampered by lack of a suitable animal model. Our aim was to develop a novel animal model...

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Detalles Bibliográficos
Autores principales: Fang, Shun-Miao, Zhang, Qing-Hua, Jiang, Zhi-Xin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2682487/
https://www.ncbi.nlm.nih.gov/pubmed/19344521
http://dx.doi.org/10.1186/1423-0127-16-39
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author Fang, Shun-Miao
Zhang, Qing-Hua
Jiang, Zhi-Xin
author_facet Fang, Shun-Miao
Zhang, Qing-Hua
Jiang, Zhi-Xin
author_sort Fang, Shun-Miao
collection PubMed
description BACKGROUND: It is widely believed that atherosclerotic plaque rupture and subsequent thrombosis leads to acute coronary events and stroke. However, study of the mechanism and treatment of human plaque rupture is hampered by lack of a suitable animal model. Our aim was to develop a novel animal model of atherosclerotic plaque rupture to facilitate the study of human plaque disruption and thrombosis. METHODS: 28 healthy male New Zealand white rabbits were randomly divided into two groups: rabbits in group A (n = 12) were only fed a high-fat diet for eight weeks; rabbits in group B (n = 16) underwent cold-induced endothelial injury with liquid nitrogen, then were given a high-fat diet for eight weeks. After completion of the preparatory regimen, triggering of plaque rupture was attempted by local injection of liquid nitrogen in both groups. RESULTS: All rabbits in group B had disrupted plaques or rupture-driven occlusive thrombus formation, but none in group A showed any effects. More importantly, the cold-induced plaques in our model were reminiscent of human atherosclerotic plaques in terms of architecture, cellular composition, growth characteristics, and patterns of lipid accumulation. CONCLUSION: We successfully developed a novel rabbit model of atherosclerotic plaque rupture and thrombosis, which is simple, fast, inexpensive, and reproducible, and has a low mortality and a high yield of triggering. This model will allow us to better understand the mechanism of human plaque rupture and also to develop plaque-stabilizing therapies.
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spelling pubmed-26824872009-05-15 Developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury Fang, Shun-Miao Zhang, Qing-Hua Jiang, Zhi-Xin J Biomed Sci Research BACKGROUND: It is widely believed that atherosclerotic plaque rupture and subsequent thrombosis leads to acute coronary events and stroke. However, study of the mechanism and treatment of human plaque rupture is hampered by lack of a suitable animal model. Our aim was to develop a novel animal model of atherosclerotic plaque rupture to facilitate the study of human plaque disruption and thrombosis. METHODS: 28 healthy male New Zealand white rabbits were randomly divided into two groups: rabbits in group A (n = 12) were only fed a high-fat diet for eight weeks; rabbits in group B (n = 16) underwent cold-induced endothelial injury with liquid nitrogen, then were given a high-fat diet for eight weeks. After completion of the preparatory regimen, triggering of plaque rupture was attempted by local injection of liquid nitrogen in both groups. RESULTS: All rabbits in group B had disrupted plaques or rupture-driven occlusive thrombus formation, but none in group A showed any effects. More importantly, the cold-induced plaques in our model were reminiscent of human atherosclerotic plaques in terms of architecture, cellular composition, growth characteristics, and patterns of lipid accumulation. CONCLUSION: We successfully developed a novel rabbit model of atherosclerotic plaque rupture and thrombosis, which is simple, fast, inexpensive, and reproducible, and has a low mortality and a high yield of triggering. This model will allow us to better understand the mechanism of human plaque rupture and also to develop plaque-stabilizing therapies. BioMed Central 2009-04-04 /pmc/articles/PMC2682487/ /pubmed/19344521 http://dx.doi.org/10.1186/1423-0127-16-39 Text en Copyright © 2009 Fang 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 Research
Fang, Shun-Miao
Zhang, Qing-Hua
Jiang, Zhi-Xin
Developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury
title Developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury
title_full Developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury
title_fullStr Developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury
title_full_unstemmed Developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury
title_short Developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury
title_sort developing a novel rabbit model of atherosclerotic plaque rupture and thrombosis by cold-induced endothelial injury
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2682487/
https://www.ncbi.nlm.nih.gov/pubmed/19344521
http://dx.doi.org/10.1186/1423-0127-16-39
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