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大鼠胰十二指肠移植缺血-再灌注损伤模型的建立 被引量:5

Establishment of ischemia-reperfusion injury model of pancreaticoduodenal transplantation in rats
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摘要 目的 探索胰腺移植缺血 再灌注损伤 (I RI)的发生机制及防治措施。方法 采用双套管 +移植物腹主动脉三通管外接法完成大鼠全胰十二指肠同种异体移植动物模型。实验分为A、B组 ,每组 15只 ,分别于术后 6、2 4h处死。处死时检测非空腹血糖 ,并行移植物组织学观察。结果  3 0次实验中 ,总手术时间仅为 2h左右 ,移植手术成功率 10 0 %。排除因套管内血栓形成引起移植物失功的 3例外 ,其余受试大鼠血糖水平均在术后 6或 2 4h降至正常 ,移植胰功能存活率为90 % (2 7/3 0 )。A、B两组组织学改变符合I RI病生特点。结论 本模型操作简便、稳定 ,不需阻断体循环 ,具有术后移植物功能恢复早的优点 。 Objective To explore the mechanism and prevention ischemia reperfusion injury (I RI) of pancreas transplantation.Methods The animal model of whole pancreaticoduodenal allotransplantation was developed by using the technique of dual cannula combined with abdominal aorta connected with te.All recipient rats divided into group A ( n =15) and B ( n =15) were respectively sacrificed at 6 h and 24 h after transplantation to examine glucose level of non fasting blood samples and histological changes of graft.Results 30 operations were performed.The total procedure of transplantation lasted about 2 h.The successful rate of operation was elevated to 100%.Except 3 cases of graft non function because of thrombosis in cannula,the glucose level of the remaining recipients was reduced to normal level at posttransplantaion 6 h or 24 h.The survival rate of graft function was 90% (27/30).The histological changes of two groups were coincident with those characteristic of I RI.Conclusion It is a simple and stable model without blocking systemic circulation.This model could recover the function of graft in advanced.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2003年第10期944-945,共2页 Chinese Journal of Experimental Surgery
关键词 胰腺移植 十二指肠移植 再灌注损伤 发生机制 防治 大鼠 Pancreas Transplantation Reperfusion injury Mode,animal
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参考文献1

  • 1Sun Lee, Kenneth SKT, Koopmans H, et al. Pancreaticoduodenal transplantation in the rat. Transplantation, 1972, 13:421-425.

同被引文献36

  • 1倪晓光,关凤林,刘忠,陈海龙,尚东,王长淼.大鼠全胰十二指肠移植术并发症的分析及预防[J].大连医科大学学报,2001,23(1):43-44. 被引量:1
  • 2朱兴国,田清水,陈彦,李德春.大鼠胰十二指肠移植动物模型的制作[J].中华实验外科杂志,2005,22(4):496-497. 被引量:15
  • 3虞俊波,徐泽宽.肠造瘘式大鼠胰十二指肠移植模型的建立[J].中华实验外科杂志,2006,23(1):109-109. 被引量:3
  • 4Alain LM, Michel G, Antel A, et al. Multiple pathways to allograft rejection. Transplantation, 2002, 73:1373-1381.
  • 5Sekine Y, Yasufuku K, Heidler KM, et al. Monocyte chemoattractant protein-1 and RANTES are chemotactic for graft infiltrating lymphocytes during acute lung allograft rejection. Am J Respir Cell Mol Biol,2000, 23: 719-726.
  • 6Nakhleh RE, Sutherland DER, Tzardis P, et al. Correlation of rejection of the duodenum with rejection of the pancreas in a pig model of pancreaticoduodenal transplantation. Translplantation, 1993, 56: 1353-1356.
  • 7John AB, Robert MS. Chemokines/chemokine receptors play an important role in the continuum of acute to chronic lung allograft rejection.Current Opinion in Organ Transplantation, 2004, 9:350-360.
  • 8Mulligan H, McDuffie JE, Shanley TP, et al. Role of RANTES in experimental cardiac allograft rejection. Exp Mol Pathol, 2000, 69: 167-174.
  • 9Sekine Y, Yasufuku K, Heidler KM, et al. Monocyte chemoattractant protein-1and RANTES are chemotactic for graft infiltrating lymphocytes during acute lung allograft rejection. Am J Respir Cell Mol Biol,2000, 23: 719-726.
  • 10Shoskes DA. Effect of bioflavonoids quercetin and curcumin on ischemic renal injury: a new class of renoprotective agents. Transplantation, 1998, 66:147-152.

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