Aldosterone and D-glucose stimulate the proliferation of human cardiac myofibroblasts in vitro

被引:87
作者
Neumann, S
Huse, K
Semrau, R
Diegeler, A
Gebhardt, R
Buniatian, GH
Scholz, GH
机构
[1] Univ Leipzig, Dept Internal Med 3, D-04103 Leipzig, Germany
[2] Univ Leipzig, Dept Internal Med 2, D-04103 Leipzig, Germany
[3] Univ Leipzig, Dept Heart & Cardiovasc Surg, D-04103 Leipzig, Germany
[4] Univ Leipzig, Inst Biochem, D-04103 Leipzig, Germany
[5] Univ Cologne, Dept Radiat Oncol, Cologne, Germany
[6] Univ Cologne, Inst Mol Biotechnol, Cologne, Germany
关键词
aldosterone; glucose; cardiac myofibroblasts; human;
D O I
10.1161/hy0302.105295
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The renin-angiotensin-aldosterone-system appears to be involved in the development of cardiac fibrosis in rodents, characterized by nonepithelial cell proliferation and changes in the extracellular matrix. The aim of our study was to investigate the effect of high aldosterone concentrations on the proliferation of human cardiac interstitial cells in vitro. In addition, the effect of D-glucose as another risk factor for Fibrosis, eg, in the diabetic heart, was investigated. Human cardiac myofibroblast cultures were established, and growth rates were measured by WST-1 assay in fetal calf scrum-free Dulbecco's modified Eagle's medium (DMEM). Cells in culture showed a significant increase in number between 24 to 72 hours of cultivation under basal conditions (DMEM, 10% fetal calf serum). Aldosterone at high concentrations (10(-8) and 10(-7) mol/L) significantly (P < 0.01) increased the proliferation of cultured cardiac myofibroblasts. Comparable effects were observed after incubation of the cells with high D-glucose concentrations (15 and 25 mmol/L, P < 0.01). No additive growth stimulation was evident when the cells were incubated in medium containing both aldosterone and D-glucose. These results suggest a role for aldosterone and glucose in mediating the cardiac fibrosis through stimulation of myofibroblast growth in patients with dysregulated renin-angiotensin-aldosterone-system (especially hyperaldosteronism) and impaired glucose homeostasis.
引用
收藏
页码:756 / 760
页数:5
相关论文
共 37 条
[31]   HIGH GLUCOSE-INDUCED PROLIFERATION IN MESANGIAL CELLS IS REVERSED BY AUTOCRINE TGF-BETA [J].
WOLF, G ;
SHARMA, K ;
YING, C ;
ERICKSEN, M ;
ZIYADEH, FN .
KIDNEY INTERNATIONAL, 1992, 42 (03) :647-656
[32]   Aldosterone mediates angiotensin II-stimulated rat vascular smooth muscle cell proliferation [J].
Xiao, F ;
Puddefoot, JR ;
Vinson, GP .
JOURNAL OF ENDOCRINOLOGY, 2000, 165 (02) :533-536
[33]   Role of PKC and TGF-β receptor in glucose-induced proliferation of smooth muscle cells [J].
Yasuda, Y ;
Nakamura, J ;
Hamada, Y ;
Nakayama, M ;
Chaya, S ;
Naruse, K ;
Nakashima, E ;
Kato, K ;
Kamiya, H ;
Hotta, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 281 (01) :71-77
[34]   DETERMINANTS OF CARDIAC FIBROSIS IN EXPERIMENTAL HYPERMINERALOCORTICOID STATES [J].
YOUNG, M ;
HEAD, G ;
FUNDER, J .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1995, 269 (04) :E657-E662
[35]   Cardiac steroidogenesis in the normal and failing heart [J].
Young, MJ ;
Clyne, CD ;
Cole, TJ ;
Funder, JW .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (11) :5121-5126
[36]  
Yusuf S, 2000, NEW ENGL J MED, V342, P145
[37]   Limitation of excessive extracellular matrix turnover may contribute to survival benefit of spironolactone therapy in patients with congestive heart failure - Insights from the Randomized Aldactone Evaluation Study (RALES) [J].
Zannad, F ;
Alla, F ;
Dousset, B ;
Perez, A ;
Pitt, B .
CIRCULATION, 2000, 102 (22) :2700-2706