Department of Cardiovascular Surgery, Inselspital, Bern University Hospital, Bern, Switzerland; Department for BioMedical Research, University of Bern, Bern, Switzerland.
Center of Laboratory Medicine, University Institute of Clinical Chemistry, University Hospital, Inselspital, Bern, Switzerland.
J Heart Lung Transplant. 2019 Jul;38(7):767-777. doi: 10.1016/j.healun.2019.03.004. Epub 2019 Mar 13.
Donation after circulatory death (DCD) could significantly improve cardiac graft availability. However, DCD hearts undergo potentially deleterious warm ischemia/reperfusion (I/R). As endothelial damage is a key factor in cardiac I/R injury, we aimed to investigate the tolerance of cardiac and endothelial function after various durations of warm ischemia to improve the timing and choice of cardioprotective therapies.
Isolated, working rat hearts were perfused for 20 minutes aerobically, then underwent various periods of warm global ischemia and either 30 or 60 minutes of reperfusion.
Compared with non-ischemic hearts, recovery of left ventricular work (heart rate-developed pressure product) was significantly reduced at 60 minutes of reperfusion with ≥27 minutes of ischemia (p <0.05 for all), but was unchanged after 21 or 24 minutes of ischemia. Markers of cell death and edema significantly increased with ≥27-minute ischemia compared with non-ischemic hearts (p <0.05 for all). Endothelial-dependent vasodilation was significantly impaired compared with non-ischemic hearts with ≥24 minutes of ischemia, whereas endothelial-independent vasodilation was impaired with ≥27 minutes of ischemia (p <0.05 for all). Furthermore, with ≥24 minutes of ischemia, superoxide production by nitric oxide synthase and peroxynitrite levels were significantly increased compared with non-ischemic hearts, suggesting endothelial nitric oxide synthase (eNOS) uncoupling (p <0.05 for both).
The first signs of endothelial dysfunction after cardiac ischemia occur with less ischemia than cardiac functional alterations, and may result from increased eNOS uncoupling. Strategies aimed at improving eNOS coupling may thus help to optimize both endothelial and myocardial recovery, ultimately facilitating DCD heart transplantation.
心脏死亡后捐献(DCD)可以显著提高心脏移植物的可获得性。然而,DCD 心脏经历潜在的有害热缺血/再灌注(I/R)。由于内皮损伤是心脏 I/R 损伤的关键因素,我们旨在研究不同时间的热缺血后心脏和内皮功能的耐受性,以改善心脏保护治疗的时机和选择。
分离的、工作状态的大鼠心脏在有氧条件下灌注 20 分钟,然后经历不同时间的热全缺血,再灌注 30 或 60 分钟。
与非缺血心脏相比,缺血时间≥27 分钟时,60 分钟再灌注时左心室工作(心率-压力乘积)的恢复明显降低(p<0.05),但缺血时间为 21 或 24 分钟时则不变。与非缺血心脏相比,缺血时间≥27 分钟时细胞死亡和水肿标志物明显增加(p<0.05)。与非缺血心脏相比,缺血时间≥24 分钟时内皮依赖性血管舒张明显受损,而内皮非依赖性血管舒张则在缺血时间≥27 分钟时受损(p<0.05)。此外,与非缺血心脏相比,缺血时间≥24 分钟时一氧化氮合酶的超氧化物产生和过氧亚硝酸盐水平明显增加,表明内皮型一氧化氮合酶(eNOS)解偶联(p<0.05)。
心脏缺血后内皮功能障碍的第一个迹象发生在比心脏功能改变更少的缺血时间,可能是由于 eNOS 解偶联增加所致。旨在改善 eNOS 偶联的策略可能有助于优化内皮和心肌恢复,最终促进 DCD 心脏移植。