Controlled Reperfusion Strategies Improve Cardiac Hemodynamic Recovery after Warm Global Ischemia in an Isolated, Working Rat Heart Model of Donation after Circulatory Death (DCD)

被引:15
作者
Farine, Emilie [1 ,2 ]
Niederberger, Petra [1 ,2 ]
Wyss, Rahel K. [1 ,2 ]
Mendez-Carmona, Natalia [1 ,2 ]
Gahl, Brigitta [1 ,2 ]
Fiedler, Georg M. [3 ]
Carrel, Thierry P. [1 ,2 ]
Stahel, Hendrik T. Tevaearai [1 ,2 ]
Longnus, Sarah L. [1 ,2 ]
机构
[1] Bern Univ Hosp, Inselspital, Clin Cardiovasc Surg, Bern, Switzerland
[2] Univ Bern, Dept Clin Res, Bern, Switzerland
[3] Univ Hosp Bern, Inselspital, Ctr Lab Med, Univ Inst Clin Chem, Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
acidic reperfusion; cardioprotection; donation after circulatory death; heart transplantation; hypoxia; ischemia reperfusion injury; mechanical postconditioning; mild hypothermia; MITOCHONDRIAL PERMEABILITY TRANSITION; ACUTE MYOCARDIAL-INFARCTION; CARDIOPROTECTIVE THERAPIES; POSTCONDITIONING PROTECTS; MILD HYPOTHERMIA; LOW-PRESSURE; INJURY; TRANSPLANTATION; PERFUSION; CARDIOMYOCYTE;
D O I
10.3389/fphys.2016.00543
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Aims: Donation after circulatory death (DCD) could improve cardiac graft availability, which is currently insufficient to meet transplant demand. However, DCD organs undergo an inevitable period of warm ischemia and most cardioprotective approaches can only be applied at reperfusion (procurement) for ethical reasons. We investigated whether modifying physical conditions at reperfusion, using four different strategies, effectively improves hemodynamic recovery after warm ischemia. Methods and Results: Isolated hearts of male Wistar rats were perfused in working-mode for 20 min, subjected to 27 min global ischemia (37 degrees C), and 60 min reperfusion (n = 43). Mild hypothermia (30 degrees C, 10 min), mechanical postconditioning (MPC; 2x 30 s reperfusion/30 s ischemia), hypoxia (no O-2, 2 min), or low pH (pH 6.87.4, 3 min) was applied at reperfusion and compared with controls (i.e., no strategy). After 60 min reperfusion, recovery of left ventricular work (developed pressure*heart rate; expressed as percent of pre-ischemic value) was significantly greater for mild hypothermia (62 +/- 7%), MPC (65 +/- 8%) and hypoxia (61 +/- 11%; p < 0.05 for all), but not for low pH (45 +/- 13%), vs. controls (44 +/- 7%). Increased hemodynamic recovery was associated with greater oxygen consumption (mild hypothermia, MPC) and coronary perfusion (mild hypothermia, MPC, hypoxia), and with reduced markers of necrosis (mild hypothermia, MPC, hypoxia) and mitochondrial damage (mild hypothermia, hypoxia). Conclusions: Brief modifications in physical conditions at reperfusion, such as hypothermia, mechanical postconditioning, and hypoxia, improve post-ischemic hemodynamic function in our model of DCD. Cardioprotective reperfusion strategies applied at graft procurement could improve DCD graft recovery and limit further injury; however, optimal clinical approaches remain to be characterized.
引用
收藏
页数:11
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