Tevaearai Hendrik T, Walton G Brant, Eckhart Andrea D, Keys Janelle R, Koch Walter J
Departments of Surgery and Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA.
J Thorac Cardiovasc Surg. 2002 Dec;124(6):1149-56. doi: 10.1067/mtc.2002.127315.
Recent studies have demonstrated cardiac improvement in patients supported with a ventricular assist device, suggesting that reverse remodeling and myocardial recovery are possible. We developed an animal model of cardiac unloading by adapting a heterotopic transplantation technique and used it to examine the pattern of functional recovery in the left ventricle of the failing heart.
Heart failure was induced in adult New Zealand rabbits by coronary artery ligation with subsequent myocardial infarction. Animals undergoing sham operation served as a control group. After 4 weeks or 3 months, failing hearts were transplanted into the necks of recipient rabbits. A left ventricular latex balloon connected to subcutaneous tubing allowed repeated physiologic analysis on days 1 and after transplantation and then every 5 days until day 30.
Contractility (left ventricular dP/dt(max)) and relaxation (left ventricular dP/dt(min)) were significantly lower in transplanted postinfarction hearts as compared to control hearts immediately after transplantation. Both left ventricular dP/dt(max) and left ventricular dP/dt(min) responses to increased preload and to beta-adrenergic stimulation progressively improved to a significantly higher level after 30 days of left ventricular unloading for the hearts that were transplanted 4 weeks after myocardial infarction. However, this functional improvement was not detected in failing hearts transplanted 3 months after infarction.
This model of cardiac unloading appears at least partially to mimic conditions of ventricular assist devices. If performed early in the development of heart failure, it permits improvement of contractile dysfunction and restoration of cardiac responsiveness to mechanical and beta-adrenergic stimulation. Therefore this model may constitute a novel alternative in the study of reverse remodeling in unloaded failing hearts.
近期研究表明,接受心室辅助装置支持的患者心脏功能有所改善,这表明逆向重构和心肌恢复是可能的。我们通过改良异位移植技术建立了心脏卸载动物模型,并用于研究衰竭心脏左心室的功能恢复模式。
通过冠状动脉结扎及随后的心肌梗死诱导成年新西兰兔发生心力衰竭。接受假手术的动物作为对照组。4周或3个月后,将衰竭心脏移植到受体兔颈部。连接皮下管道的左心室乳胶球囊可在移植后第1天及之后每隔5天直至第30天进行重复生理分析。
与移植后即刻的对照心脏相比,移植后的梗死心脏收缩性(左心室dP/dt(max))和舒张性(左心室dP/dt(min))显著降低。对于心肌梗死后4周移植的心脏,在左心室卸载30天后,左心室dP/dt(max)和左心室dP/dt(min)对增加前负荷和β-肾上腺素能刺激的反应逐渐改善至显著更高水平。然而,在梗死后3个月移植的衰竭心脏中未检测到这种功能改善。
这种心脏卸载模型似乎至少部分模拟了心室辅助装置的情况。如果在心力衰竭发展早期进行,它可以改善收缩功能障碍并恢复心脏对机械和β-肾上腺素能刺激的反应性。因此,该模型可能成为研究卸载衰竭心脏逆向重构的一种新的替代方法。