Department of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Transplantation. 2011 Oct 27;92(8):858-63. doi: 10.1097/TP.0b013e31822d8778.
The use of non-heart-beating donors (NHBD) has come into practice to resolve the shortage of donor lungs. This study investigated whether hypothermic machine perfusion (HMP) can improve the quality of NHBD lungs.
An uncontrolled NHBD model was achieved in male Lewis rats. Ninety minutes after cardiac arrest, HMP was performed for 60 min at 6°C to 10°C. The first study investigated the physiological lung functions during HMP and the lung tissue energy levels before and after HMP. The second study divided the rats into three groups (n=6 each): no ischemia group; 90-min warm ischemia+60-min HMP+120-min static cold storage (SCS) (HMP group); and 90-min warm ischemia+180-min SCS group. All lungs were reperfused for 60 min at 37°C. Lung functions were evaluated at given timings throughout the experiments. Oxidative damage during reperfusion was evaluated immunohistochemically with a monoclonal antibody against 8-hydroxy-2'-deoxyguanosine.
The first study revealed that lung functions were stable during HMP. Lung tissue energy levels decreased during warm ischemia but were significantly increased by HMP (P<0.05). The second study confirmed that HMP significantly decreased pulmonary vascular resistance, increased pulmonary compliance, and improved pulmonary oxygenation. The ratio of 8-hydroxy-2'-deoxyguanosine positive cells to total cells significantly increased in the SCS group (P<0.01).
Short-term HMP improved lung tissue energy levels that decreased during warm ischemia and ameliorated ischemia-reperfusion injury with decreased production of reactive oxygen species.
为了解决供体肺短缺的问题,已经开始使用无心跳供体(NHBD)。本研究旨在探讨低温机器灌注(HMP)是否能改善 NHBD 肺的质量。
采用雄性 Lewis 大鼠建立非控制性 NHBD 模型。心脏停搏 90 分钟后,在 6°C 至 10°C 下进行 HMP 60 分钟。第一项研究在 HMP 期间调查了肺的生理功能以及 HMP 前后肺组织的能量水平。第二项研究将大鼠分为三组(每组 6 只):无缺血组;90 分钟热缺血+60 分钟 HMP+120 分钟静态冷保存(SCS)(HMP 组);90 分钟热缺血+180 分钟 SCS 组。所有肺在 37°C 下再灌注 60 分钟。在整个实验过程中,在特定时间点评估肺功能。用单克隆抗体 8-羟基-2'-脱氧鸟苷检测再灌注期间的氧化损伤。
第一项研究显示,HMP 期间肺功能稳定。热缺血期间肺组织能量水平降低,但 HMP 显著增加(P<0.05)。第二项研究证实,HMP 显著降低肺血管阻力,增加肺顺应性,改善肺氧合。SCS 组 8-羟基-2'-脱氧鸟苷阳性细胞与总细胞的比值显著增加(P<0.01)。
短期 HMP 可改善热缺血期间降低的肺组织能量水平,并通过减少活性氧的产生来改善缺血再灌注损伤。