Department of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
J Heart Lung Transplant. 2012 Oct;31(10):1136-42. doi: 10.1016/j.healun.2012.07.006. Epub 2012 Aug 22.
Warm ischemia-reperfusion injury related to donation after cardiac death is a crucial issue in transplantation. Because surfactant function deteriorates in lungs during warm ischemia, we hypothesized pre-recovery surfactant inhalation would mitigate warm ischemia-reperfusion injury.
We rendered donor dogs cardiac dead and left them at room temperature. All animals received ventilation for 60 minutes starting at 240 minutes after cardiac arrest. The animals were divided into 2 groups: NS (normal saline, n = 7) group, which received aerosolized normal saline, and SF (surfactant; n = 5), which received aerosolized surfactant. The lungs were flushed and procured, and the left lung was transplanted into recipient dogs. At 45 minutes of reperfusion, the right pulmonary artery was ligated, and the left transplanted lung function was evaluated.
In the NS group, 2 of 7 dogs died at 75 minutes after reperfusion, whereas all 5 animals in the SF group survived for 240 minutes after reperfusion. The SF group showed significantly better dynamic compliance, oxygenation, and wet-to-dry weight ratio. Furthermore, the SF group had higher levels of high-energy phosphates in the lung tissues and lower levels of interleukin-8, tumor necrosis factor-α, and protein in the bronchoalveolar lavage fluid. Histologically, the lungs in the SF group showed fewer signs of interstitial edema and hemorrhage and significantly less neutrophilic sequestration than those of the NS group.
Our results indicated pre-recovery surfactant inhalation improved graft function, maintained adenine nucleotide levels, and prevented alveolar-capillary barrier leakage, resulting in the attenuation of warm ischemia-reperfusion injury.
与心脏死亡后供体相关的热缺血再灌注损伤是移植中的一个关键问题。由于在热缺血期间肺表面活性剂功能恶化,我们假设复苏前肺表面活性剂吸入将减轻热缺血再灌注损伤。
我们使供体犬心脏死亡,并将其置于室温下。所有动物在心脏骤停后 240 分钟开始通气 60 分钟。动物分为 2 组:NS(生理盐水,n = 7)组,接受雾化生理盐水;SF(表面活性剂;n = 5)组,接受雾化表面活性剂。冲洗并采集肺部,并将左肺移植到受体犬中。在再灌注 45 分钟时,结扎右肺动脉,并评估左移植肺功能。
在 NS 组中,7 只狗中有 2 只在再灌注后 75 分钟死亡,而 SF 组中的 5 只动物在再灌注后 240 分钟全部存活。SF 组的动态顺应性、氧合和湿重/干重比明显更好。此外,SF 组肺组织中的高能磷酸水平更高,支气管肺泡灌洗液中的白细胞介素-8、肿瘤坏死因子-α和蛋白水平更低。组织学上,SF 组的肺间质水肿和出血迹象以及中性粒细胞隔离明显少于 NS 组。
我们的结果表明,复苏前肺表面活性剂吸入可改善移植物功能,维持腺嘌呤核苷酸水平,并防止肺泡毛细血管屏障渗漏,从而减轻热缺血再灌注损伤。