Iliodromitis Efstathios K, Georgiadis Michael, Cohen Michael V, Downey James M, Bofilis Elias, Kremastinos Dimitrios T
Second University Department of Cardiology, Medical School, Attikon General Hospital, University of Athens, Athens, Greece.
Basic Res Cardiol. 2006 Nov;101(6):502-7. doi: 10.1007/s00395-006-0606-3. Epub 2006 Jul 7.
Post-conditioning in the early reperfusion period confers protection to the heart after a potentially lethal episode of prolonged ischemia. Protection from this novel intervention has been documented in rat, rabbit and canine hearts, but one group has reported that it is ineffective in pigs, a large-animal species that should be most relevant to humans. We hypothesized that this negative result was related to an inappropriate post-conditioning protocol rather than the species. The present study, therefore, tested whether an effective post-conditioning protocol could be identified that limits infarct size in anesthetized pigs. Domestic Landrace pigs weighing 25-29 kg were anesthetized, and after a mid-sternal thoracotomy and pericardiotomy the left anterior descending coronary artery was ligated for 60 min followed by 3 h of reperfusion. Three groups were studied: control group (n = 5) with no other intervention, 4-30 PostC group (n = 5) with 4 cycles of 30-s reperfusion/30-s ischemia, and 8-30 PostC group (n = 6) with 8 cycles of 30-s reperfusion/30-s ischemia. The two post-conditioning protocols started immediately after termination of the 60-min coronary occlusion. Region at risk and infarct size were delineated with the aid of pre-mortem monastral blue injection and postmortem staining with triphenyltetrazolium chloride, respectively. In control hearts 33.5 +/- 7.6% of the risk zone infarcted and 36.7 +/- 3.7% in the 4-30 PostC group (P = NS). But there was only 10.5 +/- 0.5% infarction in the 8-30 PostC group (P < 0.01 vs. the other two groups). Post-conditioning confers protection in pigs but requires more than 4 ischemia/reperfusion cycles. Post-conditioning may protect by inhibiting mitochondrial permeability transition pore formation by keeping the heart acidotic as it is reoxygenated. If true, then it would be difficult to employ too many occlusion cycles.
早期再灌注期的后适应可在长时间缺血这一潜在致死性发作后为心脏提供保护。大鼠、兔和犬的心脏已证实可从这种新干预措施中获得保护,但有一组报告称其在猪(一种与人类最为相关的大型动物)中无效。我们推测这一阴性结果与不恰当的后适应方案有关,而非物种问题。因此,本研究测试了是否能确定一种有效的后适应方案,以限制麻醉猪的梗死面积。对体重25 - 29千克的家系长白猪进行麻醉,经胸骨正中切开术和心包切开术后,结扎左前降支冠状动脉60分钟,随后再灌注3小时。研究分为三组:对照组(n = 5),无其他干预;4 - 30后适应组(n = 5),进行4个周期的30秒再灌注/30秒缺血;8 - 30后适应组(n = 6),进行8个周期的30秒再灌注/30秒缺血。两种后适应方案在60分钟冠状动脉闭塞结束后立即开始。借助尸前注射莫那斯特蓝和尸后用氯化三苯基四氮唑染色分别界定危险区域和梗死面积。对照组心脏梗死面积为危险区域的33.5±7.6%,4 - 30后适应组为36.7±3.7%(P = 无显著差异)。但8 - 30后适应组梗死面积仅为10.5±0.5%(与其他两组相比,P < 0.01)。后适应可为猪提供保护,但需要超过4个缺血/再灌注周期。后适应可能通过在心脏复氧时使其保持酸中毒状态来抑制线粒体通透性转换孔的形成从而发挥保护作用。如果属实,那么采用过多的闭塞周期将很困难。