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大鼠移植动脉硬化加快模型的建立 被引量:2

Promoted transplant arteriosclerosis in a rat aortic model
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摘要 目的 建立一种简捷 ,有代表性且稳定的移植物动脉硬化模型。方法 将SD大鼠的腹主动脉分别冷缺血 1、2 4、48h行SD→SD及SD→Wistar的原位腹主动脉移植 ,观察术后植入段血管病理改变、TGF β1表达及手术前后过氧化脂质的变化。结果 SD→SD及SD→Wistar缺血1h组分别于术后 10周及 6周见内膜明显增厚 ,而缺血 2 4h组只需 2周 ;各组移植后 2h过氧化脂质均明显高于术前 ,术后 4、2 4h与术前比差异无显著性 (P >0 .0 5 ) ;强化缺血组TGF β1不论是SD→SD还是SD→Wistar均于术后 1周即出现高表达。结论 以SD/Wistar作为供 /受体行腹主动脉移植 ,强化冷缺血损伤 ,可加快移植物动脉硬化 ,可望成为新型慢排模型。 Objective To establish a novel,representative and steady transplant arteriosclerosis model.Methods Abdominal aorta grafts from SD rats were cold stored for 1,24,or 48 h before being orthopically transplanted to SD or Wistar recipients.The pathohistological changes and the expression of TGF-β1 of the grafts were observed.The changes of serum lipid peroxides pre- and post-transplantation were also measured.Results The intimal thickness of SD→SD and SD→Wistar ischemia for 1 h was significantly greated than that of pre-transplantation in 10 weeks and 6 weeks respectively,whereas grafts with 24 h of ischemia developed pronounced thickening in 2 weeks.Serum levels of lipid peroxides were significantly higher in 2 h post-transplantation in all groups than pre-transplantation,but there was no significant different pre- and 4 or 24 h post-transplantation.The staining intensity of TGF-β1 in 24 and 48 h of ischemia was stronger one week after transplantation regardless of syngeneic or allogeneic transplants.Conclusion The transplantation of abdominal aorta grafts used SD/Wistar as donors and recipients with prolonged cold ischemia time is sufficient to promote the development of transplant arteriosclerosis.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2003年第7期663-665,F003,共4页 Chinese Journal of Experimental Surgery
关键词 大鼠 主动脉移植 动脉硬化 动物模型 移植物慢性失功 Aorta Transplantation Arteriosclerosis Model,animal
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  • 1杨晓玲,赵迅霞,王菲,李桂忠,张鸣号,曹军.实验大鼠动脉粥样硬化模型的建立[J].宁夏医学院学报,2007,29(4):350-351. 被引量:31
  • 2Joosten SA,van Kooten C,Paul LC.Pathogenesis of chronic allograft rejection.Transpl Int,2003,16:137-145.
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  • 4Sayegh MH,Carpenter CB.Transplantation 50 years later-progress,challenges,and promises.N Engl J Med,2004,351:2761-2766.
  • 5Libby P,Pober JS.Chronic rejection.Immunity,2001,14:387-397.
  • 6Hu Y,Davison F,Ludewig B,et al.Smooth muscle cells in transplant atherosclerotic lesions are originated from recipients,but not bone marrow progenitor cells.Circulation,2002,106:1834-1839.
  • 7Sinclair AH,Berta P,Palmer MS,et al.A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif.Nature,1990,346:240-244.
  • 8Bradbury MW,Isola LM,Gordon JW.Enzymatic amplification of a Y chromosome repeat in a single blastomere allows identification of the sex of preimplantation mouse embryos.PNAS,1990,87:4053-4057.
  • 9李迎新,黄霖.动脉粥样硬化动物模型制作方法的介绍[J].中国比较医学杂志,2008,18(5):70-73. 被引量:13
  • 10闫盛,郝斌.动脉粥样硬化动物模型研究现状[J].山西医药杂志(下半月),2008,37(8):731-733. 被引量:2

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