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缺血后处理减轻大鼠后肢缺血再灌注后肺损伤的实验研究 被引量:3

Ischemic Postconditioning Attenuated Lung Injury Induced by Ischemia-reperfusion in the Hind Limbs of Rats
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摘要 目的探讨缺血后处理(I-postC)对大鼠双侧后肢缺血再灌注(I/R)后肺损伤的影响及意义。方法阻断肾下腹主动脉建立大鼠双侧后肢I/R损伤模型。48只大鼠随机分为3组:缺血再灌注(I/R)组、缺血预处理(IPC)组及I-postC组,每组再随机分为两个亚组(n=8),并分别于再灌注后12h,24h取标本。观察肺组织形态学、湿/干重比、丙二醛(MDA)及髓过氧化物酶(MPO)的变化。原位杂交和逆转录多聚酶链反应(RT-PCR)方法检测肺组织中细胞间黏附分子1(ICAM-1)的mRNA表达,Western blot检测ICAM-1蛋白表达。结果IPC组和I-postC组的各项指标均明显减少,与I/R组比较差异十分显著(P<0.01),但两组之间差异不显著(P>0.05)。结论I-postC能减轻大鼠双侧后肢缺血再灌注后肺损伤,与IPC可能存在共同的作用机制。 Objective To study the effect of ischemic postconditioning(I-postC)on the lung injury following ischemia-reperfusion(I/R)in the hind limbs of rats.Methods The rat model of hind limbs I/R injury was established by subrenal abdominal aorta cross-clamping for 4 hours.48 rats were divided into 3 groups:I/R group,IPC and I-postC group.Each group received 4 hours of ischemia and then 12 hours or 24 hours of reperfusion respectively.The tissue morphology,wet-to-dry weight(W/D)ratio,malondialdehyde(MDA)and myeloperoxidase(MPO)in lung were compared.The mRNA expression of ICAM-1 in lung was also studied by RT-PCR or in situ hybridization.The protein product was detected by Western blot.Results In IPC and I-postC group,all parameters decreased significantly compared with I/R ischemia group(P〈 0.01).There was no significantly difference between the IPC and I-postC group(P 〈0.05).Conclusion I-postC can attenuate lung injury following skeletal muscle I/R in the hind limbs of rats,which maybe accomplished by inhibition of adhesion and infiltration of polymorphonuclear neutrophil(PMN).
出处 《中国医科大学学报》 CAS CSCD 北大核心 2010年第4期245-247,共3页 Journal of China Medical University
基金 国家自然科学基金资助项目(30600631 30672048)
关键词 缺血后处理 缺血再灌注 骨骼肌 肺损伤 ischemic postconditioning ischemia-reperfusion skeletal muscle lung injury
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  • 1[1]Tassiopoulos AK, Carlin RE, Gao Y, et al. Role of nitric oxide and tumor necrosis factor on lung injury caused by ischemia/reperfusion of the lower extremities [ J ]. J Vasc Surg , 1997, 26 (4): 647 -656.
  • 2[2]Kyriakides C, Austen W, Wang Y, et al. Skeletal muscle reperfusion injury is mediated by neutrophils and the complement membrane attack complex[J]. Am J Physiol, 1999, 277 (6 Pt 1 ):C1263 - C1268.
  • 3[3]Anderson BO, Brown JM, Harken AH, et al. Mechanisms of neutrophilmediated tissue injury [ J ]. J Surg Res, 1991, 51 ( 2 ):170 - 179.
  • 4[4]Gaines GC, Welborn MB, Moldawer LL,et al. Attenuation of skeletal muscle ischemia/reperfusion injury by inhibition of tumor necrosis factor[J]. J Vasc Surg, 1999, 29(2): 370 -376.
  • 5[5]Kelly KJ, Williams WW, Colvin RB, et al. Intercellular adhesion molecule-l-deficient mice are protected against ischemic renal injury [J]. J Clin Invest, 1996, 97(4): 1056 -1063.

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