Donate Help Contact The AHA Sign In Home
American Heart Association
Arteriosclerosis, Thrombosis, and Vascular Biology
Search: search_blue_button Advanced Search
Arteriosclerosis, Thrombosis, and Vascular Biology. 2007;27:453
doi: 10.1161/01.ATV.0000257138.15250.48
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Eitzman, D. T.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Eitzman, D. T.
Related Collections
Right arrow Regulation of Hemostasis and Thrombosis: Murine Models
Right arrowRelated Article
(Arteriosclerosis, Thrombosis, and Vascular Biology. 2007;27:453.)
© 2007 American Heart Association, Inc.


ATVB In Focus

Regulation of Hemostasis and Thrombosis

Insights from Murine Models

Daniel T. Eitzman

From the Division of Cardiovascular Medicine, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor.

Correspondence to Daniel T. Eitzman, MD, 1150 W. Medical Center Dr., 7301 MSRB III, Ann Arbor, MI 48109-0644. E-mail deitzman@umich.edu


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 

This issue of Arteriosclerosis, Thrombosis, and Vascular Biology contains the first of a series of articles describing the use of murine models to explore the regulation of hemostasis and thrombosis.

See page 454

Thrombotic complications of atherosclerosis, such as myocardial infarction and stroke, remain the leading cause of mortality in the Western world. Despite advances in therapies such as statins, which retard the progression of atherosclerosis and reduce vascular complications, myocardial infarction and stroke continue to dominate the healthcare system. Thus there is an urgent need to develop effective chronic therapeutic interventions for prevention of these thrombotic vascular complications. Current treatment is limited in part because of insufficient knowledge regarding the important regulatory factors in atherothrombosis and also because therapies targeting this process may also impair hemostasis leading to bleeding complications. Therapeutic interventions are similarly limited for prophylaxis of deep venous thrombosis and thrombi occurring in the atrial appendages. It is also likely that different factors affect the predisposition to thrombosis in different disease states and vascular beds, and that disease-specific antithrombotic treatments will be necessary.

Because thrombosis appears to be affected by many factors, including circulating blood cells, the vessel wall, blood flow patterns, and many other unknown elements, an in vivo model may be required to accurately assess the impact of potential important regulatory factors. Because mice are particularly amenable to genetic manipulation, the mouse has become a valuable tool to study thrombosis. There are now several models of induced and spontaneous thrombosis available in the mouse. The . . . [Full Text of this Article]


Related Article:

Heparin Cofactor II Modulates the Response to Vascular Injury
Douglas M. Tollefsen
Arterioscler Thromb Vasc Biol 2007 27: 454-460. [Abstract] [Full Text] [PDF]