The development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyrene

Yong Zhang1, Kenneth S Ramos1,21Department of Biochemistry and Molecular Biology, University of Louisville School of Medicine, Louisville, KY, USA; 2Center for Genetics and Molecular Medicine, University of Louisville, Louisville, KY, USAAbstract: Cigarette smoking has been strongly associated with...

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Main Authors: Yong Zhang, Kenneth S Ramos
Format: Article
Language:English
Published: Dove Medical Press 2008-10-01
Series:Vascular Health and Risk Management
Subjects:
Online Access:https://www.dovepress.com/the-development-of-abdominal-aortic-aneurysms-in-mice-is-enhanced-by-b-peer-reviewed-article-VHRM
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spelling doaj-9719b77cdf704642acf8fa92dd35acf52020-11-25T01:43:55ZengDove Medical PressVascular Health and Risk Management1178-20482008-10-01Volume 4109511021770The development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyreneYong ZhangKenneth S RamosYong Zhang1, Kenneth S Ramos1,21Department of Biochemistry and Molecular Biology, University of Louisville School of Medicine, Louisville, KY, USA; 2Center for Genetics and Molecular Medicine, University of Louisville, Louisville, KY, USAAbstract: Cigarette smoking has been strongly associated with abdominal aortic aneurysm (AAA), but the components of tobacco smoke involved in AAA have not been identified. Benzo(a)pyrene (BaP) is an important constituent in cigarette smoke capable of induction of alterations strikingly similar to the pathological changes seen during AAA development. We therefore hypothesized that BaP exposure contributes to the development of AAA. In this study, C57/B6J mice were treated with vehicle, angiotensin II (AngII) (0.72 mg/kg/day), BaP (10 mg/kg/week), or the combination of AngII and BaP, for 5 weeks, and then examined for incidence of AAA and pathological changes of the aortic wall. Results showed that incidence of AAA formation in C57/B6J mice treated with BaP and AngII was significantly higher than that in AngII-treated mice (7 of 12 compared to 2 of 12). Further, five mice in the group treated with AngII/BaP and one in the group treated with AngII exhibited AAA rupture and hematoma. BaP caused macrophage infi ltration, disarray of elastic lamella, and loss of vascular smooth muscle cells (VSMCs). We conclude that BaP aggravates AAA formation and rupture in C57/B6J mice by promoting macrophage infi ltration, degeneration of elastic lamella, and loss of VSMCs in the aortic wall.Keywords: abdominal aortic aneurysm, benzo(a)pyrene, cigarette smoking, aorta, C57B/6J micehttps://www.dovepress.com/the-development-of-abdominal-aortic-aneurysms-in-mice-is-enhanced-by-b-peer-reviewed-article-VHRMAbdominal Aortic AneurysmBenzo(a)pyrenCigarette SmokingAortaC57B/6J Mice
collection DOAJ
language English
format Article
sources DOAJ
author Yong Zhang
Kenneth S Ramos
spellingShingle Yong Zhang
Kenneth S Ramos
The development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyrene
Vascular Health and Risk Management
Abdominal Aortic Aneurysm
Benzo(a)pyren
Cigarette Smoking
Aorta
C57B/6J Mice
author_facet Yong Zhang
Kenneth S Ramos
author_sort Yong Zhang
title The development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyrene
title_short The development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyrene
title_full The development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyrene
title_fullStr The development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyrene
title_full_unstemmed The development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyrene
title_sort development of abdominal aortic aneurysms in mice is enhanced by benzo(a)pyrene
publisher Dove Medical Press
series Vascular Health and Risk Management
issn 1178-2048
publishDate 2008-10-01
description Yong Zhang1, Kenneth S Ramos1,21Department of Biochemistry and Molecular Biology, University of Louisville School of Medicine, Louisville, KY, USA; 2Center for Genetics and Molecular Medicine, University of Louisville, Louisville, KY, USAAbstract: Cigarette smoking has been strongly associated with abdominal aortic aneurysm (AAA), but the components of tobacco smoke involved in AAA have not been identified. Benzo(a)pyrene (BaP) is an important constituent in cigarette smoke capable of induction of alterations strikingly similar to the pathological changes seen during AAA development. We therefore hypothesized that BaP exposure contributes to the development of AAA. In this study, C57/B6J mice were treated with vehicle, angiotensin II (AngII) (0.72 mg/kg/day), BaP (10 mg/kg/week), or the combination of AngII and BaP, for 5 weeks, and then examined for incidence of AAA and pathological changes of the aortic wall. Results showed that incidence of AAA formation in C57/B6J mice treated with BaP and AngII was significantly higher than that in AngII-treated mice (7 of 12 compared to 2 of 12). Further, five mice in the group treated with AngII/BaP and one in the group treated with AngII exhibited AAA rupture and hematoma. BaP caused macrophage infi ltration, disarray of elastic lamella, and loss of vascular smooth muscle cells (VSMCs). We conclude that BaP aggravates AAA formation and rupture in C57/B6J mice by promoting macrophage infi ltration, degeneration of elastic lamella, and loss of VSMCs in the aortic wall.Keywords: abdominal aortic aneurysm, benzo(a)pyrene, cigarette smoking, aorta, C57B/6J mice
topic Abdominal Aortic Aneurysm
Benzo(a)pyren
Cigarette Smoking
Aorta
C57B/6J Mice
url https://www.dovepress.com/the-development-of-abdominal-aortic-aneurysms-in-mice-is-enhanced-by-b-peer-reviewed-article-VHRM
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