Takahashi S
First Department of Surgery, Hirosaki University School of Medicine, Japan.
Nihon Kyobu Geka Gakkai Zasshi. 1993 Jun;41(6):995-1007.
Some effectiveness of free radical scavengers for the prevention of reperfusion injury are reported, however those scavengers do not perfectly repel the reperfusion injury and do not widely used to avoid that insult. This study was undertaken to assess why free radical scavengers do not be so effective to prevent the reperfusion injury. The heart-lung transplantation was performed according to the method of Schäfers. Explanted heart-lung block was immersed and preserved in the University of Wisconsin solution excluding allopurinol for just 4 hours at 4 degrees C. The recipients were divided into three groups: group I (n = 8), mimetic group with lactated Ringer's solution, group II (n = 7), animals treated with allopurinol, and group III (n = 7), animals treated with superoxide dismutase (SOD) and catalase (CAT). All scavengers were administered during preservation and reperfusion process. Graft function was evaluated by max dp/dt and partial pressure of oxygen in pulmonary venous blood. Free radicals generated in the plasma obtained from the pulmonary vein and coronary sinus were measured, using electron spin resonance (ESR) spectrometry and the production of free radicals from the neutrophils obtained from the pulmonary vein was measured by chemiluminescence. In group II and III, the grafts got significantly better restore than in group I in cardiac and respiratory function until 30 min after reperfusion, but the graft's function in group I gradually detenorated at 60 min after reperfusion. ESR spectra were deteriorated and indicated a hyperfine splitting constant of aN = 1.55 mT, aH beta = 0.28 mT suggesting the presence of PBN-OH, ESR signals were significantly higher and showed a marked increase in group I than in group II after reperfusion.(ABSTRACT TRUNCATED AT 250 WORDS)
据报道,自由基清除剂在预防再灌注损伤方面有一定效果,然而这些清除剂并不能完全抵御再灌注损伤,也未被广泛用于避免这种损伤。本研究旨在评估自由基清除剂预防再灌注损伤效果不佳的原因。心肺移植按照施费尔斯的方法进行。取出的心肺块在不含别嘌呤醇的威斯康星大学溶液中于4℃浸泡保存4小时。受体被分为三组:第一组(n = 8),用乳酸林格氏液的模拟组;第二组(n = 7),用别嘌呤醇治疗的动物组;第三组(n = 7),用超氧化物歧化酶(SOD)和过氧化氢酶(CAT)治疗的动物组。所有清除剂均在保存和再灌注过程中给予。通过最大dp/dt和肺静脉血氧分压评估移植物功能。使用电子自旋共振(ESR)光谱法测量从肺静脉和冠状窦获得的血浆中产生的自由基,并通过化学发光法测量从肺静脉获得的中性粒细胞产生的自由基。在第二组和第三组中,直到再灌注后30分钟,移植物的心脏和呼吸功能恢复明显优于第一组,但第一组移植物的功能在再灌注后60分钟逐渐恶化。ESR光谱恶化,表明超精细分裂常数aN = 1.55 mT,aHβ = 0.28 mT,提示存在PBN - OH,再灌注后第一组的ESR信号明显更高且显著增加,高于第二组。(摘要截短于250字)