Desrois M, Piccardo A, Zogheib E, Dalmasso C, Lan C, Fourré D, Cozzone P J, Caus T, Bernard M
Aix-Marseille Université, CNRS, CRMBM UMR 7339 Marseille, France.
Service de Chirurgie Cardiaque, CHU Amiens-Picardie, Amiens, France.
Transplant Proc. 2014 Dec;46(10):3314-8. doi: 10.1016/j.transproceed.2014.04.021.
We measured the functional and metabolic status of hearts submitted to normothermic ischemia before preservation through the use of an ex vivo pig heart model to assess the feasibility of donation after cardiac death (DCD) in heart transplantation.
Ten pigs were separated into 2 groups: control (n = 6, brain-dead group) and DCD (n = 4, heart donation after cardiac death). In the control group, hearts were excised 20 minutes after the brachiocephalic trunk cross-clamping and were immediately reperfused. In DCD, hearts were excised 20 minutes after exsanguination and asphyxia, stored in the Centre de Résonance Magnétique Biologique et Médicale (CRMBM) solution for 2 hours, and then were reperfused. Cardioplegic arrest was induced with the use of 1 L of CRMBM solution (4°C) and the heart was reperfused for 60 minutes through the use of an ex vivo perfusion system in Langendorff mode with normothermic autologous blood. During reperfusion, functional parameters were analyzed. Biochemical assays were performed in myocardial effluents and freeze-clamped hearts.
No electromechanical activity was found in DCD compared with control. Creatine kinase (CK) was higher at 2 minutes of reperfusion in DCD versus control (P = .005). Adenosine triphosphate was lower in DCD versus control (P = .0019). Malondialdehyde, an oxidative stress index, was present only in DCD. The nitric oxide (NO) pathway was impaired in DCD versus control, with lower eNOS expression (P < .0001) and total nitrate concentration content (P = .04).
We reported no cardiac functional and metabolic recovery in the DCD group after normothermic ischemia and reperfusion, which indicates that a single immersion of the cardiac graft during storage does not provide an optimal protection. New strategies in heart preservation are necessary for recruiting heart donation after cardiac death.
我们通过使用离体猪心模型,测量了在保存前经历常温缺血的心脏的功能和代谢状态,以评估心脏移植中心源性死亡后捐赠(DCD)的可行性。
将10只猪分为2组:对照组(n = 6,脑死亡组)和DCD组(n = 4,心源性死亡后心脏捐赠)。在对照组中,在头臂干交叉钳夹20分钟后切除心脏并立即进行再灌注。在DCD组中,放血和窒息20分钟后切除心脏,在生物与医学磁共振中心(CRMBM)溶液中保存2小时,然后进行再灌注。使用1升CRMBM溶液(4°C)诱导心脏停搏,并通过使用Langendorff模式的离体灌注系统用常温自体血使心脏再灌注60分钟。在再灌注期间,分析功能参数。在心肌流出液和冷冻钳夹的心脏中进行生化测定。
与对照组相比,DCD组未发现电机械活动。再灌注2分钟时,DCD组的肌酸激酶(CK)高于对照组(P = .005)。DCD组的三磷酸腺苷低于对照组(P = .0019)。氧化应激指标丙二醛仅在DCD组中存在。与对照组相比,DCD组的一氧化氮(NO)途径受损,内皮型一氧化氮合酶(eNOS)表达较低(P < .0001),总硝酸盐浓度含量较低(P = .04)。
我们报告常温缺血和再灌注后DCD组心脏功能和代谢未恢复,这表明在保存期间心脏移植物的单次浸泡不能提供最佳保护。需要新的心脏保存策略来招募心源性死亡后的心脏捐赠。