Elami Amir, Gavish Zohar, Korach Amit, Houminer Esther, Schneider Aviva, Schwalb Herzl, Arav Amir
The Department of Cardiothoracic Surgery and the Joseph Lunenfeld Cardiac Surgery Research Center, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
J Thorac Cardiovasc Surg. 2008 Mar;135(3):666-72, 672.e1. doi: 10.1016/j.jtcvs.2007.08.056.
Long-term organ preservation for transplantation may allow optimal donor-recipient matching with potential reduction in the incidence and severity of rejection. Complete cessation of metabolism may be obtained by freezing. Previous attempts to freeze intact mammalian hearts were limited to -3.6 degrees C, restricting tissue ice content to 34%. We hypothesized that our method will allow recovery of function of the intact rat heart after freezing to -8 degrees C, a temperature at which most of the tissue water is frozen.
Isolated rat hearts were attached to a Langendorff apparatus. After normothermic perfusion, cold cardioplegia was induced followed by perfusion with a cryoprotecting agent. Hearts were than frozen to -8 degrees C (45 +/- 8 minutes), thawed, and reperfused (60 minutes).
All frozen and thawed hearts regained normal electric activity. At -8 degrees C, ice content was 64.36% +/- 13%. The use of 10% ethylene glycol for cryoprotection (n = 13) resulted in recovery (mean +/- standard deviation) of 49.7% +/- 21.8% of +dP/dt, 48.0% +/- 23.5% of -dP/dt, 65.2% +/- 30.8% of coronary flow, and 50.4% +/- 23.9% of left ventricular developed pressure. Hearts in this group (n = 4) maintained 81.3% +/- 10% viability compared with 69.3% +/- 14% (not significant) in control hearts kept at 0 degrees C for the same duration. Energy stores, represented by adenosine triphosphate and phosphocreatine, were depleted to 12.2 +/- 6.1 micromol/g dry weight and 22.5 +/- 6.4 micromol/g dry weight, respectively, compared with 19.0 +/- 2.5 micromol/g dry weight and 36.6 +/- 3.0 micromol/g dry weight, respectively (P < .05) in the control hearts. The integrity of muscle fibers and intracellular organelles after thawing and reperfusion was demonstrated by electron microscopy.
We demonstrate for the first time the feasibility of functional recovery after freezing and thawing of the isolated rat heart while maintaining structural integrity and viability.
长期保存用于移植的器官可能会实现供体与受体的最佳匹配,并有可能降低排斥反应的发生率和严重程度。通过冷冻可使新陈代谢完全停止。此前将完整的哺乳动物心脏冷冻的尝试仅限于-3.6摄氏度,这使得组织中的冰含量限制在34%。我们推测,我们的方法将使完整的大鼠心脏在冷冻至-8摄氏度(此时大部分组织水分已冻结)后恢复功能。
将离体大鼠心脏连接到Langendorff装置上。在常温灌注后,诱导冷停搏,随后灌注冷冻保护剂。然后将心脏冷冻至-8摄氏度(45±8分钟),解冻并再灌注(60分钟)。
所有冷冻和解冻后的心脏都恢复了正常电活动。在-8摄氏度时,冰含量为64.36%±13%。使用10%乙二醇进行冷冻保护(n = 13)后,+dP/dt恢复了49.7%±21.8%,-dP/dt恢复了48.0%±23.5%,冠状动脉血流恢复了65.2%±30.8%,左心室舒张末压恢复了50.4%±23.9%。该组心脏(n = 4)的存活率维持在81.3%±10%,而在0摄氏度下保存相同时间的对照心脏存活率为69.3%±14%(无显著差异)。以三磷酸腺苷和磷酸肌酸表示的能量储备分别降至12.2±6.1微摩尔/克干重和22.5±6.4微摩尔/克干重,而对照心脏分别为19.0±2.5微摩尔/克干重和36.6±3.0微摩尔/克干重(P <.05)。解冻和再灌注后肌肉纤维和细胞内细胞器的完整性通过电子显微镜得以证实。
我们首次证明了离体大鼠心脏冷冻和解冻后功能恢复的可行性,同时保持了结构完整性和存活率。