Angiogenic and cardiac functional effects of dual gene transfer of VEGF-A165 and PDGF-BB after myocardial infarction

被引:24
作者
Hao, XJ
Månsson-Broberg, A
Blomberg, P
Dellgren, G
Siddiqui, AJ
Grinnemo, KH
Wärdell, E
Sylvén, C
机构
[1] Karolinska Inst, Dept Cardiol, Stockholm, Sweden
[2] Karolinska Univ Hosp, Stockholm, Sweden
[3] Karolinska Inst, NOVUM, Gene Therapy Ctr, Stockholm, Sweden
[4] Karolinska Inst, Dept Cardiothorac Surg & Anaesthesiol, Stockholm, Sweden
关键词
angiogenesis; arteriogenesis; VEGF-A(165); PDGF-BB; plasmid; myocardial infarction;
D O I
10.1016/j.bbrc.2004.07.101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Therapeutic angiogenesis is a potential treatment modality for myocardial ischemia. phVEGF-A(165), phPDGF-BB, or a combination of the two were injected into the myocardial infarct border zone in rats 7 days after ligation of the coronary left anterior descending artery. Cardiac function was measured by echocardiography. Hearts were harvested 1 and 4 weeks after plasmid injection. phVEGF-A(165) increased capillary density more than phPDGF-BB, and phPDGF-BB preferentially stimulated arteriolar growth. The combination increased both capillaries and arterioles but did not enhance angiogenesis any more than single plasmid treatments did. VEGF-A(165) and the combination of phVEGF-A(165) and phPDGF-BB counteracted left ventricular dilatation after I week but did not counteract further deterioration. (C) 2004 Published by Elsevier Inc.
引用
收藏
页码:292 / 296
页数:5
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