Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Sign In to gain access to subscriptions and/or personal tools.
Toxicologic Pathology
This Article
Right arrow Free Full Text Free
Right arrow Free Full Text (Free PDF) Free
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Boor, P. J.
Right arrow Articles by Gong, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Boor, P. J.
Right arrow Articles by Gong, B.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Articles

Role of the Media in Vascular Injury: Atherosclerosis and Dissection

Paul J. Boor, Yonzhen Yang and Bin Gong

Department of Pathology, University of Texas Medical Branch, Galveston, Texas, 77555, USA

Correspondence: Address correspondence to: Paul J. Boor, Department of Pathology, University of Texas Medical Branch at Galveston, 301 University Blvd, Galveston, Texas 77555-0609, USA; e-mail:pboor{at}utmb.edu

Although a metabolic role for endothelium in toxic injury has been well established, a similar role has not been as thoroughly explored for the vascular media. In this study two forms of vascular medial involvement in toxic injury are examined. Early atherosclerotic plaques are studied by immunohistochemistry for an {alpha} class glutathione-S-transferase (GST) isozyme known as hGSTA4-4, which has preferential metabolic activity for {alpha}, β-unsaturated aldehydes derived from lipid peroxidation, especially 4-hydroxy-2-nonenal. Findings in human plaque indicate that hGST A4-4 is highly upregulated in vascular smooth muscle cells (VSMCs) within the plaque and in the medial VSMCs underlying plaque. Endothelial cells, while not expressing hGST A4-4 distant from plaques, were found to express the isozyme in cytoplasm overlying plaque. In a series of second experiments, we illustrate a developmental model of dissecting aortic aneurysm (DAA) obtained by administering semicarbazide, an inhibitor of the little-studied VSMC enzyme semicarbazide-sensitive amine oxidase (SSAO), to pregnant rats during the last trimester of development. Newborn rats consistently developed DAA which is characterized by splitting of media of ascending thoracic aorta and extensive blood collections surrounding the vessel. These experimental examples emphasize the potential role of the media in toxic insults to blood vessels. Also, the potential importance of toxic injury to developing blood vessels by in utero exposure to xenobiotic substances is illustrated.

Key Words: Toxicology • aorta • vascular media • vascular smooth muscle cells • atherosclerosis • glutathione-S-transferase • semicarbazide-sensitive amine oxidase • dissecting aortic aneurysm

Abbreviations: DAA, Dissecting Aortic Aneurysm • VSMC, vascular smooth muscle cell • GST, glutathione-S-transferase • 4-HNE, 4-hydroxy-2-nonenal • SSAO, semicarbazide-sensitive amine oxidase • VAP-1, vascular adhesion protein-1 • H+E, hematoxylin and eosin

Toxicologic Pathology, Vol. 34, No. 1, 33-38 (2006)
DOI: 10.1080/01926230500369907


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?