Di Lascio Gabriella, Harmelin Guy, Targetti Mattia, Nanni Cristina, Bianchi Giacomo, Gasbarri Tommaso, Gelsomino Sandro, Bani Daniele, Orlandini Sandra Zecchi, Bonacchi Massimo
Department of Medical & Surgical Critical Area, Cardiac Surgery Unit, University of Florence, 50141 Florence, Italy.
Tex Heart Inst J. 2012;39(4):488-99.
We sought to determine whether skeletal myoblasts, wild-type or engineered to express relaxin, might improve myocardial viability and performance in a rat model of chronic myocardial infarction. Our purpose was to investigate a potential new therapy for heart failure. From October 2005 through September 2009, we surgically induced acute myocardial infarction in 80 male Wistar rats. Thirty days after surgery, the rats underwent reoperation for the retrograde coronary venous infusion of skeletal myoblasts, relaxin, or both. The animals were randomly assigned to 4 experimental groups: R1 (the control group, which underwent saline-solution infusion), R2 (systemic relaxin therapy), R3 (myoblast infusion), and R4 (myoblast infusion and systemic relaxin therapy). Echocardiography, positron emission tomography, and cellular and histologic analysis were performed at 4 established time points. Mortality rates were similar among the groups. Postinfarction echocardiographic evaluation revealed similar left ventricular dysfunction. Viable myocardium, evaluated with positron emission tomography, was analogous. After therapy, the echocardiographic values of cardiac function improved significantly (P<0.05) in all groups except R1. Myocardial viability volume increased significantly in groups R3 and R4 (P<0.05) but was unchanged in groups R2 and R1. In group R4, the echocardiographic and positron emission tomographic results improved significantly (P<0.001). Histologic analysis showed that myoblasts settled in regions of ischemic scarring, especially when combined with relaxin. The retrograde venous route is safe, effective, and clinically feasible for cell delivery. Myoblasts and relaxin are better than either alone in terms of myocardial viability and performance improvement.
我们试图确定野生型或经基因工程改造以表达松弛素的骨骼肌成肌细胞,是否能改善慢性心肌梗死大鼠模型的心肌活力和功能。我们的目的是研究一种潜在的心力衰竭新疗法。从2005年10月至2009年9月,我们通过手术诱导80只雄性Wistar大鼠发生急性心肌梗死。术后30天,大鼠接受再次手术,通过逆行冠状静脉输注骨骼肌成肌细胞、松弛素或两者。动物被随机分为4个实验组:R1(对照组,接受盐溶液输注)、R2(全身松弛素治疗组)、R3(成肌细胞输注组)和R4(成肌细胞输注及全身松弛素治疗组)。在4个既定时间点进行超声心动图、正电子发射断层扫描以及细胞和组织学分析。各组的死亡率相似。梗死后超声心动图评估显示左心室功能障碍相似。用正电子发射断层扫描评估的存活心肌情况类似。治疗后,除R1组外,所有组的心脏功能超声心动图值均显著改善(P<0.05)。R3组和R4组的心肌存活体积显著增加(P<0.05),而R2组和R1组未改变。在R4组,超声心动图和正电子发射断层扫描结果显著改善(P<0.001)。组织学分析表明,成肌细胞定位于缺血性瘢痕区域,尤其是与松弛素联合使用时。逆行静脉途径用于细胞递送是安全、有效的,且在临床上可行。在改善心肌活力和功能方面,成肌细胞和松弛素联合使用比单独使用任何一种都更好。