帮助 关于我们

返回检索结果

Cardiac autonomic nerve fiber regeneration in chronic heart failure Do Akt gene-transduced mesenchymal stem cells promote repair?

查看参考文献56篇

文摘 BACKGROUND: Transplantation of Akt-over-expressing mesenchymal stem cells (Akt-MSCs) has been shown to repair infarcted myocardium and improve cardiac function. However, little is known about the therapeutic effects of Akt-MSCs on cardiac autonomic neuropathy in chronic heart failure (CHF). OBJECTIVE: The present study used adriamycin-induced CHF rat models to observe the effect of Akt-MSCs on cardiac autonomic nervous regeneration and the factors mediating this effect. DESIGN, TIME AND SETTING: A randomized, controlled animal experiment was performed at the Central Laboratory of Basic Medical College, China Medical University, between September 2008 and April 2009.MATERIALS: Rabbit anti-choline acetyltransferase (ChAT), growth associated protein-43 (GAP-43), synaptophysin (SYN) polyclonal antibodies and the secondary antibody (goat anti-rabbit IgG) were purchased from Boster, China. Cat-A-Kit assay system was provided by Amersham, USA.METHODS: (1) Adult rat MSCs were isolated and cultured for the preparation of Akt-MSCs. (2) Forty male Wistar rats were intramyocardially administered adriamycin at 2 mg/kg over 3 days for a total of five times and once a week for additional five times thereafter to establish CHF models. At 2 weeks after final adriamycin treatment, 34 successful CHF rat models were randomized to three groups: Akt-MSCs (n = 11), simple MSCs (s-MSCs, n =11), and control (n = 12). Each group was intravenously administered Akt-MSCs (2×10~6 cells in 100 μL PBS), s-MSCs (2×10~6 cells in 100 μL PBS) or equal volume of phosphate buffered saline, once a day for a total of three times. MAIN OUTCOME MEASURES: At 4 weeks after final adriamycin treatment, myocardial norepinephrine (NE) content was detected using a Cat-A-Kit assay system. Myocardial ChAT, SYN and GAP-43 were performed by immunohistochemistry and Western blot analysis. Prior to, 2 and 4 weeks after adriamycin treatment, echocardiographic examination was performed and left ventricular ejection fraction (LVEF) was determined. RESULTS: Myocardial NE content, as well as SYN-positive and GAP-43-positive nerve fiber density and expression, and LVEF, was the greatest in the Akt-MSCs group, followed by the s-MSCs group, and lastly the control group (P < 0.05 or P < 0.01). ChAT expression was similar between Akt-MSCs and s-MSCs groups, but it was higher compared with the control group (P < 0.05). NE contents were negatively correlated to LVEF (r = -0.64, P = 0.015). CONCLUSION: Transplantation of MSCs, in particular Akt-MSCs, promotes cardiac nervous regeneration in failing heart, which might be mediated by GAP-43.
来源 Neural Regeneration Research ,2010,5(1):28-34 【核心库】
DOI 10.3969/j.issn.1673-5374.2010.01.005
关键词 mesenchymal stem cells ; Akt gene transfection ; chronic heart failure ; neural regeneration ; autonomic nerve system
地址

1. Department of Cardiology, the First Affiliated Hospital of China Medical University, Liaoning, Shenyang, 110001  

2. Department of Cardiology, the People's Hospital of Liaoning Province, Liaoning, Shenyang, 110016  

3. Shenyang Normal University, Liaoning, Shenyang, 110034

语种 英文
文献类型 研究性论文
ISSN 1673-5374
学科 神经病学与精神病学
基金 Scientific Research Program of Higher Education Institute in Liaoning Province
文献收藏号 CSCD:3821755

参考文献 共 56 共3页

1.  Braunwald E. Congestive heart failure:fifty years of progress. CIRCULATION,2000,102(20 Suppl 4):IV14-IV23 CSCD被引 50    
2.  Aydin M. Cardiac autonomic activity in obstructive sleep apnea:time-dependent and spectral analysis of heart rate variability using 24-hour Hoher electrocardiograms. Texas Heart Institute Journal,2004,31(2):132-136 CSCD被引 11    
3.  Pittenger MF. Mesenchymal stem cells and their potential as cardiac therapeutics. CIRCULATION RESEARCH,2004,95:9-20 CSCD被引 95    
4.  Amado LC. Cardiac repair with intramyocardial injection of allogeneic mesenchymal stem cells after myocardial infarction. Proceedings of the National Academy of Sciences(USA),2005,102(32):11474-11479 CSCD被引 51    
5.  Tomita S. Improved heart function with myogenesis and angiogenesis after autologous porcine bone marrow stromal cell transplantation. Journal of Thoracic and Cardiovascular Surgery,2002,123:1132-1140 CSCD被引 88    
6.  Gojo S. In vivo cardiovasculogenesis by direct injection of isolated adult mesenchymal stem cells. Experimental Cell Research,2003,288:51-59 CSCD被引 29    
7.  Dai W. Allogeneic mesenchymal stem cell transplantation in postinfarcted rat myocardium:short-and long-term effects. CIRCULATION,2005,112:214-223 CSCD被引 66    
8.  Kong HL. Cell multiplication,apoptosis and p-Akt protein expression of bone mesenchymal stem cells of rat under hypoxia environment. Journal of Nanjing Medical University,2007,21(4):233-239 CSCD被引 4    
9.  Kong HL. Apoptosis and proliferation of rat bone marrow mesenchymal stem cells transfected by Akt gene under hypoxia. Zhongguo Zuzhi Huaxue yu Xibao Huaxue Zazhi,2008,17(3):225-231 CSCD被引 1    
10.  Noiseux N. Mesenchymal stem cells overexpressing Akt dramatically repair infarcted myocardium and improve cardiac function despite infrequent cellular fusion or differentiation. Molecular Therapy,2006,14(6):840-850 CSCD被引 22    
11.  Gnecchi M. Evidence supporting paracrine hypothesis for Akt-modified mesenchymal stem cell-mediated cardiac protection and functional improvement. FASEB JOURNAL,2006,20(6):661-669 CSCD被引 53    
12.  Mirotsou M. Secreted frizzled related protein 2 (Sfrp2) is the key Akt-mesenchymal stem cell-released paracrine factor mediating myocardial survival and repair. Proceedings of the National Academy of Sciences(USA),2007,104(5):1643-1648 CSCD被引 14    
13.  Teraoka K. Progressive cardiac dysfunction in adriamycin-induced cardiomyopathy rats. European Journal of heart failure,2000,2(4):373-378 CSCD被引 13    
14.  Li SG. A modified rat model of dilated cardiomyopathy induced by adriamycin. Zhongguo Bijiao Yixue Zazhi,2006,16(7):415-418 CSCD被引 2    
15.  Liang C. Alterations by norepinephrine of cardiac sympathetic nerve terminal function and myocardial beta-adrenergic receptor sensitivity in the ferret:normalization by antioxidant vitamins. CIRCULATION,2000,102(1):96-103 CSCD被引 3    
16.  Yang XP. Echocardiographic assessment of cardiac function in conscious and anesthetized mice. American Journal of Physiology,1999,277:H1967-H1974 CSCD被引 5    
17.  Lefrak EA. A clinicopathologic analysis of adriamycin cardiotoxicity. CANCER,1973,32:302-314 CSCD被引 18    
18.  Singal PK. Doxorubicin-induced cardiomyopathy. New England Journal of Medicine,1998,339:900-905 CSCD被引 44    
19.  Arola OJ. Acute doxorubicin cardiotoxicity involves cardiomyocyte apoptosis. CANCER RESEARCH,2000,60:1789-1792 CSCD被引 16    
20.  Kumar D. Apoptosis in adriamycin cardiomyopathy and its modulation by probucol. Antioxidants and Redox Signaling,2001,3:135-145 CSCD被引 10    
引证文献 6

1 赵颖军 Akt基因转染的骨髓间充质干细胞对心力衰竭大鼠的心脏自主神经保护效应 广东医学,2010,31(23):3027-3029
CSCD被引 0 次

2 孔宏亮 人参皂甙Rbl对阿霉素心力衰竭大鼠致心脏纤维化因子表达的影响 南京医科大学学报. 自然科学版,2012,32(1):26-29
CSCD被引 10

显示所有6篇文献

论文科学数据集
PlumX Metrics
相关文献

 作者相关
 关键词相关
 参考文献相关

版权所有 ©2008 中国科学院文献情报中心 制作维护:中国科学院文献情报中心
地址:北京中关村北四环西路33号 邮政编码:100190 联系电话:(010)82627496 E-mail:cscd@mail.las.ac.cn 京ICP备05002861号-4 | 京公网安备11010802043238号