Lack of Association Between Adiponectin Levels and Atherosclerosis in Mice

被引:55
作者
Nawrocki, Andrea R. [3 ,4 ]
Hofmann, Susanna M. [8 ]
Teupser, Daniel [10 ]
Basford, Joshua E. [8 ]
Durand, Jorge L. [5 ,6 ]
Jelicks, Linda A. [5 ,6 ]
Woo, Connie W. [11 ,12 ,13 ,14 ]
Kuriakose, George [11 ,12 ,13 ,14 ]
Factor, Stephen M. [7 ]
Tanowitz, Herbert B. [7 ]
Hui, David Y. [9 ]
Tabas, Ira [11 ,12 ,13 ,14 ]
Scherer, Philipp E. [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Touchstone Diabet Ctr, Dept Internal Med, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Touchstone Diabet Ctr, Dept Cell Biol, Dallas, TX 75390 USA
[3] Merck Res Labs, Dept Obes, Rahway, NJ USA
[4] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USA
[5] Albert Einstein Coll Med, Dept Physiol, Bronx, NY 10467 USA
[6] Albert Einstein Coll Med, Dept Biophys, Bronx, NY 10467 USA
[7] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10467 USA
[8] Univ Cincinnati, Coll Med, Dept Internal Med, Div Endocrinol, Cincinnati, OH USA
[9] Univ Cincinnati, Coll Med, Dept Pathol, Cincinnati, OH USA
[10] Univ Leipzig, Inst Lab Med Clin Chem & Mol Diagnost, Leipzig, Germany
[11] Columbia Univ, Dept Physiol, New York, NY 10027 USA
[12] Columbia Univ, Dept Med, New York, NY 10027 USA
[13] Columbia Univ, Dept Pathol, New York, NY 10027 USA
[14] Columbia Univ, Dept Cell Biol, New York, NY 10027 USA
基金
瑞士国家科学基金会;
关键词
atherosclerosis; diabetes mellitus; insulin resistance; metabolism; low-density lipoprotein receptor; adiponectin; ACTIVATED-RECEPTOR-GAMMA; ADIPOSE-SPECIFIC PROTEIN; MYOCARDIAL-INFARCTION; MACROPHAGE APOPTOSIS; INSULIN SENSITIVITY; PPAR-GAMMA; LESIONS; RESISTANCE; TISSUE; MOUSE;
D O I
10.1161/ATVBAHA.109.195826
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective-Adiponectin is an adipocyte-derived, secreted protein that is implicated in protection against a cluster of related metabolic disorders. Mice lacking adiponectin display impaired hepatic insulin sensitivity and respond only partially to peroxisome proliferator-activated receptor gamma agonists. Adiponectin has been associated with antiinflammatory and antiatherogenic properties; however, the direct involvement of adiponectin on the atherogenic process has not been studied. Methods and Results-We crossed adiponectin knockout mice (Adn(-/-)) or mice with chronically elevated adiponectin levels (Adn(Tg)) into the low-density lipoprotein receptor-null (Ldlr(-/-)) and the apoliprotein E-null (Apoe(-/-)) mouse models. Adiponectin levels did not correlate with a suppression of the atherogenic process. Plaque volume in the aortic root, cholesterol accumulation in the aorta, and plaque morphology under various dietary conditions were not affected by circulating adiponectin levels. In light of the strong associations reported for adiponectin with cardiovascular disease in humans, the lack of a phenotype in gain-and loss-of-function studies in mice suggests a lack of causation for adiponectin in inhibiting the buildup of atherosclerotic lesions. Conclusion-These data indicate that the actions of adiponectin on the cardiovascular system are complex and multifaceted, with a minimal direct impact on atherosclerotic plaque formation in preclinical rodent models. (Arterioscler Thromb Vasc Biol. 2010; 30: 1159-1165.)
引用
收藏
页码:1159 / U182
页数:19
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