11β-hydroxysteroid dehydrogenase type 1 gene expression is increased in ascending aorta tissue of metabolic syndrome patients with coronary artery disease

被引:10
作者
Atalar, F. [1 ]
Vural, B. [2 ]
Ciftci, C. [3 ]
Demirkan, A. [2 ,4 ]
Akan, G. [5 ]
Susleyici-Duman, B. [6 ]
Gunay, D. [7 ]
Akpinar, B. [8 ,9 ]
Sagbas, E. [8 ,9 ]
Ozbek, U. [2 ]
Buyukdevrim, A. S. [10 ]
机构
[1] Istanbul Univ, Inst Child Hlth, Dept Growth Dev & Pediat Endocrinol, Istanbul, Turkey
[2] Istanbul Univ, Inst Expt Med, Dept Genet, Istanbul, Turkey
[3] Istanbul Bilim Univ, Fac Med, Dept Cardiol, Istanbul, Turkey
[4] Erasmus Univ, Div Genet Epidemiol, Med Ctr, Dept Epidemiol & Biostat, Rotterdam, Netherlands
[5] Istanbul Bilim Univ, Fac Med, Dept Med Biol & Genet, Istanbul, Turkey
[6] Marmara Univ, Sci & Art Fac, Dept Biol, Istanbul, Turkey
[7] Florence Nightingale Hosp, Biochem Lab, Istanbul, Turkey
[8] Istanbul Bilim Univ, Fac Med, Dept Cardiovasc Surg, Istanbul, Turkey
[9] Istanbul Bilim Univ, Fac Med, Florence Nightingale Hosp, Istanbul, Turkey
[10] Turkish Diabet Consortium, Istanbul, Turkey
关键词
11 beta-hydroxysteroid dehydrogenase type 1; Ascending aorta; Glucocorticoids; Epicardial adipose tissue; Metabolic syndrome; Coronary artery disease; EPICARDIAL ADIPOSE-TISSUE; DIET-INDUCED OBESITY; STROMAL CELLS; IN-VIVO; FAT; DIFFERENTIATION; HEART; MICE; ATHEROSCLEROSIS; INFLAMMATION;
D O I
10.4238/2012.August.31.10
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
11 beta-hydroxysteroid dehydrogenase type 1 (11 beta-HSD-1) activity and mRNA levels are increased in visceral and subcutaneous adipose tissues of metabolic syndrome subjects. We analyzed 11 beta-HSD-1 expression in human epicardial adipose (EA) and ascending aorta (AA) tissues of metabolic syndrome patients and examined their contribution to the development of coronary atherosclerosis. The 11 beta-HSD-1 expression was evaluated by qRT-PCR in EA and AA tissues of 20 metabolic syndrome patients with coronary artery disease (metabolic syndrome group) and 10 non-metabolic syndrome patients without coronary artery disease (controls). 11 beta-HSD-1 expression was increased in EA and AA tissues of the metabolic syndrome group (4.1-and 5.5-fold, respectively). A significant positive correlation was found between 11 beta-HSD-1 expression in EA tissue and waist hip ratio and 11 beta-HSD-1 expression in AA tissue and body mass index, while a negative correlation was found between 11 beta-HSD-1 expression in EA tissue and HDL. Expression of CD68, a macrophage marker, was significantly increased in both tissues of the metabolic syndrome group; it was 2-fold higher in AA tissue compared to EA tissue in the metabolic syndrome group. Our findings of increased expression of 11 beta-HSD-1 and CD68 in AA tissue of the metabolic syndrome group lead us to suggest that they contribute to coronary atherosclerosis in metabolic syndrome. This positive correlation between obesity markers and 11 beta-HSD-1 in AA and EA tissues strengthens the evidence that 11 beta-HSD-1 has a role in metabolic syndrome. To the best of our knowledge, this is the first report showing 11 beta-HSD-1 and CD68 expression in AA tissue of metabolic syndrome patients. We suggest that there is tissue-specific expression of 11 beta-HSD-1 in metabolic syndrome and associated cardiovascular disorders.
引用
收藏
页码:3122 / 3132
页数:11
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