Lopukhin S Y, Onsager D R, Conhaim R L, Southard J H, Love R B
Department of Surgery, University of Wisconsin-Madison, 53792, USA.
Ann Thorac Surg. 1999 Jan;67(1):203-7. doi: 10.1016/s0003-4975(98)01038-8.
A limitation to fully using lung transplantation for patients with end-stage lung diseases is short, safe preservation time (4 to 6 hours). Our goal is to extend this to 24 hours or more, which would greatly improve clinical lung transplantation.
We used the isolated perfused rat lung to test how two preservation solutions (low potassium dextran and University of Wisconsin solution) affected quality of lungs after 6, 12, and 24 hours of preservation. Also, we tested modifications of the University of Wisconsin solution, including reversing the ratio of Na/K, the addition of 1.5 mmol/L calcium, and the combination of calcium and butanedione monoxime, agents that improve cardiac preservation. After preservation at 4 degrees C, lungs were reperfused at 37 degrees C with a physiologically balanced solution. Pulmonary artery flow rate, airway peak inspiratory pressure, and tissue edema were used to assess degree of preservation and reperfusion injury.
Low potassium dextran solution gave poor preservation (decreased pulmonary artery flow, tissue edema) after 12 hours of cold storage. There were no differences between regular and reversed Na/K ratio University of Wisconsin solutions at 12 or 24 hours of preservation. Addition of calcium had no beneficial effect on lung preservation. However, University of Wisconsin solution with calcium and butanedione monoxime gave excellent 24-hour cold storage, with pulmonary artery flow rate, tissue edema, and airway peak inspiratory pressure equal to control (0 hours of preservation) lungs.
The University of Wisconsin solution appears capable of lung preservation for up to 24 hours if modified to contain calcium and butanedione monoxime. The mechanism of action of butanedione monoxime may be related to the suppression of smooth muscle contraction resulting in vasodilation of the cold-stored lung on reperfusion.
终末期肺病患者充分利用肺移植的一个限制因素是安全保存时间短(4至6小时)。我们的目标是将其延长至24小时或更长时间,这将极大地改善临床肺移植。
我们使用离体灌注大鼠肺来测试两种保存液(低钾右旋糖酐和威斯康星大学保存液)在保存6、12和24小时后对肺质量的影响。此外,我们还测试了威斯康星大学保存液的改良配方,包括颠倒钠/钾比例、添加1.5 mmol/L钙以及将钙与丁二酮肟联合使用,丁二酮肟是可改善心脏保存的药物。在4℃保存后,肺在37℃用生理平衡溶液进行再灌注。用肺动脉流速、气道峰值吸气压力和组织水肿来评估保存和再灌注损伤的程度。
低钾右旋糖酐溶液在冷藏12小时后保存效果不佳(肺动脉血流减少、组织水肿)。在保存12或24小时时,常规和颠倒钠/钾比例的威斯康星大学保存液之间没有差异。添加钙对肺保存没有有益影响。然而,含有钙和丁二酮肟的威斯康星大学保存液在24小时冷藏后效果极佳,肺动脉流速、组织水肿和气道峰值吸气压力与对照(保存0小时)肺相当。
如果改良后的威斯康星大学保存液含有钙和丁二酮肟,似乎能够将肺保存长达24小时。丁二酮肟的作用机制可能与抑制平滑肌收缩有关,从而导致再灌注时冷藏肺血管舒张。