Influence of Transplantation of Allogenic Bone Marrow Mononuclear Cells on the Left Ventricular Remodeling of Rat after Acute Myocardial Infarction

被引:3
|
作者
张瑞成 [1 ]
董念国 [1 ]
侯剑峰 [2 ]
法宪恩 [2 ]
机构
[1] Department of Cardiovascular Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
[2] Department of Cardiovascular Surgery, No. 2 Affiliated Hospital of Zhengzhou University
关键词
bone marrow mononuclear cell; cell transplantation; rat; acute myocardial infarction; ventricular remodeling;
D O I
暂无
中图分类号
R542.22 [];
学科分类号
1002 ; 100201 ;
摘要
To probe into the influence of transplantation of allogenic bone marrow mononuclear cells (BM-MNCs) on the left ventricular remodeling of rat after acute myocardial infarction (AMI), 60 male Wistar rats were evenly divided into three groups at random: control group 1, control group 2 and transplantation group. In control group 1, chest was opened without ligation of coronary artery; in control group 2 and transplantation group, the left anterior descending branch of coronary artery was ligated to establish AMI model. Prepared culture medium and allogenic BM-MNCs suspension were respectively implanted the surrounding area of infracted cardiac muscle via epicardium of con-trol group 2 and transplantation group. Four weeks after the operation, the osteopontin gene (OPN mRNA, P<0.01), typeⅠcollagen (P<0.01) and angiotensin Ⅱ (AngⅡ, P<0.01) content in the left ventricular non-infracted myocardium, and the AngⅡ density in blood plasma (P<0.05) of trans-plantation group and control group 2 were all significantly higher than that of control group 1. In the transplantation group, the myocardial OPN mRNA, type Ⅰ collagen and Ang Ⅱ content of non-infracted zone in left ventricle, and the AngⅡ concentration in blood plasma were all signifi-cantly lower than those of control group 2 (P<0.05 for all). It is concluded that allogenic BM-MNCs transplantation may ease left ventricular remodeling after AMI by inhibiting the synthesis of typeⅠ collagen in the cardiac muscle and down-regulating the expression of AngⅡ and OPN gene.
引用
收藏
页码:696 / 699
页数:4
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