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大鼠肾脏缺血再灌注损伤模型的建立及稳定性观察 被引量:3

Kidney Ischemia-Reperfusion Injury Model in Rat and Observation of Its Stability
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摘要 目的通过大鼠自体原位肾移植建立肾脏缺血再灌注损伤(ischemia-reperfusion injury,IRI)模型,并观察其稳定性。方法雄性SD大鼠30只,假手术组(A组)10只,自体原位肾移植组(B组)10只,观察模型稳定性组(C组)10只。A组:不行左肾蒂血管阻断和灌注,无IRI,而单纯低温保存左肾4 h后结扎右肾蒂;B组和C组:左肾蒂血管阻断和灌注,低温保存4 h后结扎右肾蒂,开放血流。A组和B组取血和左肾检查,C组观察存活情况。结果B组4 h2、4 h的血肌酐、尿素氮水平明显高于A组,差异有显著性(p<0.01);A组大鼠肾脏未见明显病理改变,而B组呈典型的IRI改变;C组大鼠均健康存活2周,无感染发生。结论该大鼠肾脏IRI模型的建立操作简便,手术难度低、成功率高,稳定性良好,是研究肾移植IRI的理想动物模型。 Objective To establish a model of kidney ischemia-reperfusion injury(IRI) in rat with auto-orthotopic kidney transplantation, and to observe its stability. Methods Male Sprague-Dawley rats (n = 30) were divided into 3 groups: group A, sham operated group (n-- 10), group B, auto-orthotopic kidney transplantation group (n = 10) and group C, observation on the stability group (n = 10). Group A: The right kidney pedicle was ligated at 4 h after low-temperature preservation of the left kidney without occluding pedicle and perfusion. Group B: the left kidney pedicle was occluded, and the left kidney was perfused with low-temperature ( 1℃ to 4℃ ) sodium lactate Ringer' s solution by puncturing the left kidney artery, until it turned pale and the outflow from the left kidney vein became clear. Then the kidney artery and vein were repaired with atraumatic suture, The perfused kidney was preserved with the low-temperature preservation system for 4 hours, then reperfused after ligation of the right kidney pedicle. Blood and kidney sample were collected in group A and group B. In group C, the viability was observed, Results Group B had significantly higher serum ereatinine and BUN at 4 and 24 hours than that of group A (p 〈 0.01 ), Typical pathological changes of IRI were observed in group B, and no obvious changes in group A. All rats in group C had a healthy survival time over 14 days, without infection. Conclusion The model rats have advantages of mild operative difficulty, better stability, without the interference of graft rejection, and are more closely and successfully to simulate the process of lowtemperature preservation in clinical kidney transplantation. Therefore it is an ideal model for IRI studies in kidney transplantation.
出处 《中国比较医学杂志》 CAS 2006年第2期100-103,共4页 Chinese Journal of Comparative Medicine
关键词 再灌注损伤 肾移植 大鼠 SPRAGUE-DAWLEY 模型 动物 Reperfusion injury Kidney transplantation Rat, Sprague-Dawley Model, animaI
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参考文献10

  • 1Hariharan S, Johnson CP, Bresnahan BA. Improved graft survival after renal transplantation in the United States, 1988 to 1996[J]. N Engl J, 2000, 342:605-612.
  • 2Shoskes DA, Parfrey NA, Halloran PF. Increased major histocompatibility complex antigen expression in uni-lateral ischemia acute tubular necrosis in the mouse [J]. Transplant, 1990, 49: 201-207.
  • 3Azuma H, Nadeau K, Takada M, et al. Cellular molecular predictors of a single kidney[J].Transplant, 1997, 64:192-197.
  • 4张世林,闵志廉,朱有华.缺血再灌注损伤对移植肾的影响[J].肾脏病与透析肾移植杂志,1998,7(5):485-490. 被引量:5
  • 5Ojo AO, Wolfe RA, Held PJ, et al. Delayed graft function: risk factors and implications for renal allograft survival[J]. Transplant, 1997, 63:968-974.
  • 6Yokoyama H, Uchida K, Kobayashi T. Effect of prolonged delayed graft function on long term outcome in cadaveric kidney transplantation[J]. Clin Transplant, 1994,8: 101-106.
  • 7朱佳庚,张炜,钱立新,孟小鑫.一种大鼠肾移植模型的建立[J].中华实验外科杂志,2004,21(1):103-104. 被引量:29
  • 8胡建庭,赵高贤,李登宝.大鼠肾移植模型建立方法与比较[J].河南大学学报(医学科学版),2003,22(2):19-20. 被引量:6
  • 9刘小友,于立新,徐达传,孙煦勇,袁谦.大鼠肾脏移植的应用解剖[J].中国临床解剖学杂志,2004,22(3):307-309. 被引量:8
  • 10田龙,罗小敏,刘芸,金化民,王玲珑.大鼠自体原位肾移植缺血再灌注损伤模型的建立[J].武汉大学学报(医学版),2001,22(3):202-204. 被引量:8

二级参考文献22

  • 1罗小军,颜大胜.不阻断腹主动脉下腔静脉的大鼠原位肾脏移植术[J].中华显微外科杂志,1989,12(2):87-89. 被引量:1
  • 2于国中.小动物的肾移植[J].显微外科,1980,3:211-212.
  • 3Duminy F J. A new microvascular "Sleeve" anastomosis[J]. J Surg Res,1989,46: 189-194
  • 4Engelbrecht G, Delawir K, Francosis D, et al. New rapid technipue for renal transplantation in the rat[J]. Microsurgery, 1992,13:340 - 344.
  • 5J. Chin, R Zhong, Duff, and C. Stiller. Microsurgical Renal transplant models in rats: A Comparison of four anastomotic techniques[J]. Transplantation Proceedings, 1989,21 (2) : 3351 - 3352.
  • 6Fisher B, Lee S. Microvascular surgical techniques in research, with special reference to renal transplantation in the rat [J]. Surgery, 1965, 58(7): 904~914.
  • 7Fabre J, Lin SH, Morris P. Renal transplantation in the rat. Details of the techniques[J]. Aut NZ J Surg. 1971, 41(1): 69~75.
  • 8Zhang Z, Schlachta C, Stiller C, et al. Improved techniques for kidney transplantation in mice[J]. Microsurgery, 1995, 16(2): 103~109.
  • 9Jacobson JH, Suarez EL. Microsurgery in anastomosis of small vessels[J].Surgery Forum, 1960, 11: 243.
  • 10Ibrahim S, Jacobs F, Zukin Y, et al. Imumunohistochemical manifestation of unilateral ischemia. Clin Transplantation, 1996,10:646

共引文献46

同被引文献31

  • 1Gueler F, Gwinner W, Schwarz A, et al. Long-term effects of acute ischemia and reperfusion injury. Kidney Int, 2004, 66: 523-527.
  • 2Vargas GA, Hoeflich A, Jehle PM. Hepatocyte growth factor in renal failure: promise and reality. Kidney Int, 2000, 57: 1426-1436.
  • 3McMahon JM, Signori E, Wells KE, et al. Optimisation of electrotransfer of plasmid into skeletal muscle by pretreatment with hyaluronidase increased expression with reduced muscle damage. Gene Therapy, 2001, 8: 1264- 1270.
  • 4Tsujie M, Isaka Y, Nakamura H, et al. Electroporation-mediated gene transfer that targets glomeruli. J Am Soc Nephrol, 2001, 12: 949-954.
  • 5Herrero-Fresneda I, Torras J, Cruzado JM, et al. Do alloreactivity and prolonged cold ischemia cause different elementary lesions in chronic allograft nephropathy? Am J Pathol, 2003, 162:127-137.
  • 6Matsumoto K, Nakamura I. Hepatocyte growth factor: renotropic role and potential therapeutics for renal diseases. Kidney Int, 2001,59: 2023-2038.
  • 7Igawa T, Matsumoto K, Kanada S, et al. Hepatocyte growth factor may function as a renotropic factor may function as a renotropic factor for regeneration in rats with acute renal injury. Am J Physiol, 1993, 265: 639-644.
  • 8Liu ML, Mars WM, Zarnegar R, et al. Uptake and distribution of hepatocyte growth factor in nomal and regenerating adult rat liver. Am J Pathol, 1994, 144: 129- 140.
  • 9Dean DA, Machado-Aranda D, Blair-Parks K, et al. Electroporation as a method for high level nonviral gene transfer to the lung. Gene Therapy, 2002, 9: 1116-1119.
  • 10Daemen MA, Van't Veer C, Denecker G, et al. Inhibition of apoptosis induced by ischemia-reperfusion prevents inflammation. J Clin Invest, 1999, 104: 541-549.

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