Cardiac autonomic nerve fiber regeneration in chronic heart failure Do Akt gene-transduced mesenchymal stem cells promote repair?
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文摘
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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
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Neural Regeneration Research
,2010,5(1):28-34 【核心库】
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DOI
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10.3969/j.issn.1673-5374.2010.01.005
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关键词
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mesenchymal stem cells
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Akt gene transfection
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chronic heart failure
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neural regeneration
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autonomic nerve system
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地址
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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
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语种
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英文 |
文献类型
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研究性论文 |
ISSN
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1673-5374 |
学科
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神经病学与精神病学 |
基金
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Scientific Research Program of Higher Education Institute in Liaoning Province
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文献收藏号
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CSCD:3821755
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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
次
|
|
|
|
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
次
|
|
|
|
3.
Pittenger MF. Mesenchymal stem cells and their potential as cardiac therapeutics.
CIRCULATION RESEARCH,2004,95:9-20
|
CSCD被引
95
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
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
次
|
|
|
|
17.
Lefrak EA. A clinicopathologic analysis of adriamycin cardiotoxicity.
CANCER,1973,32:302-314
|
CSCD被引
18
次
|
|
|
|
18.
Singal PK. Doxorubicin-induced cardiomyopathy.
New England Journal of Medicine,1998,339:900-905
|
CSCD被引
44
次
|
|
|
|
19.
Arola OJ. Acute doxorubicin cardiotoxicity involves cardiomyocyte apoptosis.
CANCER RESEARCH,2000,60:1789-1792
|
CSCD被引
16
次
|
|
|
|
20.
Kumar D. Apoptosis in adriamycin cardiomyopathy and its modulation by probucol.
Antioxidants and Redox Signaling,2001,3:135-145
|
CSCD被引
10
次
|
|
|
|
|