Recipes for creating animal models of diabetic cardiovascular disease

被引:184
作者
Hsueh, Willa
Abel, E. Dale
Breslow, Jan L.
Maeda, Nobuyo
Davis, Richard C.
Fisher, Edward A.
Dansky, Hayes
McClain, Donald A.
McIndoe, Richard
Wassef, Momtaz K.
Rabadan-Diehl, Cristina
Goldberg, Ira J.
机构
[1] Columbia Univ, Dept Med, New York, NY 10032 USA
[2] NYU, Sch Med, Leon H Charney Div Cardiol, Marc & Ruti Bell Program Vasc Biol,Dept Med, New York, NY 10032 USA
[3] Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA 30912 USA
[4] NHLBI, Div Heart & Vasc Dis, Bethesda, MD 20892 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Div Endocrinol Diabet & Hypertens, Los Angeles, CA USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Cardiol, Los Angeles, CA USA
[7] Univ Utah, Div Endocrinol Metab & Diabet, Salt Lake City, UT USA
[8] Univ Utah, Program Human Mol Biol & Genet, Salt Lake City, UT USA
[9] Rockefeller Univ, Biochem Genet & Metab Lab, New York, NY 10021 USA
[10] Univ N Carolina, Dept Pathol & Lab Med, Chapel Hill, NC USA
关键词
atherosclerosis; diabetes mellitus; diabetic cardiomyopathy; transgenic mice;
D O I
10.1161/01.RES.0000266449.37396.1f
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
For more than 50 years, investigators have unsuccessfully tried to recreate in experimental animals the cardiovascular complications of diabetes seen in humans. In particular, accelerated atherosclerosis and dilated cardiomyopathy, the major causes of mortality in patients with diabetes, have been conspicuously absent in many mouse models of the disease. Under the auspices of the NIH, the Animal Models of Diabetic Complications Consortium has worked to address this issue. This effort has focused on the development of mouse models because of the high level of genomic information available and the many well-developed genetic manipulations that may be performed in mice. Importantly, the consortium has also worked to standardize many methods to assess metabolic and cardiovascular end points for measurement of the diabetic state and its macrovascular complications. Finally, for maximum benefits from these animal models in the study of atherosclerosis and of other diabetic complications, the consortium has created a system for sharing both the animal models and the accumulated phenotypic data with the greater scientific community.
引用
收藏
页码:1415 / 1427
页数:13
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