Kuwaki K, Komatsu K, Sohma H, Abe T
Department of Thoracic and Cardiovascular Surgery, Sapporo Medical University School of Medicine, Hokkaido, Japan.
Thorac Cardiovasc Surg. 1999 Apr;47(2):67-72. doi: 10.1055/s-2007-1013113.
We investigated the effect of lazaroid U74389G, a potent inhibitor of lipid peroxidation, on ischemia-reperfusion injury at three different doses in the rat orthotopic left lung transplantation model.
Four groups of reperfused lungs were studied. In group I (control) donor lungs were transplanted after 12 hours of preservation in University of Wisconsin (UW) solution at 4 degrees C. In groups II, III, and IV, lazaroid was used as an additive to UW solution at concentrations of 30 micromol/L, 50 micromol/L, and 100 micromol/L, respectively, and was also administered intravenously to the recipients 30 minutes before reperfusion after 12 hours of storage in the UW solution at 4 degrees C.
After 1 hour of reperfusion, gas exchange function (p < 0.01), tissue lipid peroxide levels (p < 0.05) and histologic damage in reperfused lung allografts (p< 0.05) were significantly improved in lazaroid-treated group IV compared with control group I.
These findings suggest that lazaroid U74389G ameliorates ischemia-reperfusion injury in rat lung transplants by inhibiting lipid peroxidation.
我们在大鼠原位左肺移植模型中,研究了脂质过氧化的强效抑制剂拉扎罗类药物U74389G在三种不同剂量下对缺血再灌注损伤的影响。
对四组再灌注肺进行了研究。第一组(对照组),供体肺在4℃的威斯康星大学(UW)溶液中保存12小时后进行移植。在第二、三、四组中,拉扎罗类药物分别以30微摩尔/升、50微摩尔/升和100微摩尔/升的浓度作为添加剂加入UW溶液中,并且在4℃的UW溶液中保存12小时后,在再灌注前30分钟静脉注射给受体。
再灌注1小时后,与第一对照组相比,第四组拉扎罗类药物治疗组的气体交换功能(p < 0.01)、组织脂质过氧化物水平(p < 0.05)和再灌注肺同种异体移植的组织学损伤(p < 0.05)均有显著改善。
这些发现表明,拉扎罗类药物U74389G通过抑制脂质过氧化减轻大鼠肺移植中的缺血再灌注损伤。