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内源性一氧化氮在非创伤性缺血预处理中对兔肺的保护作用
引用本文:伊力亚尔·夏合丁,罗洞波,陈雪鸿,刘春生,阿不都艾尼·吐尔洪,温浩.内源性一氧化氮在非创伤性缺血预处理中对兔肺的保护作用[J].中华器官移植杂志,2006,27(2):102-104.
作者姓名:伊力亚尔·夏合丁  罗洞波  陈雪鸿  刘春生  阿不都艾尼·吐尔洪  温浩
作者单位:1. 830054,乌鲁木齐,新疆医科大学第一附属医院胸外科
2. 新疆医科大学附属肿瘤医院胸肝外科
3. 830054,乌鲁木齐,新疆医科大学第一附属医院动物实验中心
4. 830054,乌鲁木齐,新疆医科大学第一附属医院普外科
基金项目:国家人事部留学人员科技活动择优资助项目([2003]50)
摘    要:目的探讨内源性一氧化氮(NO)在非创伤性缺血预处理(N—WIP)中对兔肺缺血/再灌注(I/R)损伤的保护作用及可能机制。方法采用N-WIP及经典缺血预处理(C-IP)的动物模型,比较两种缺血预处理方法中内源性NO对兔肺在缺血/再灌注损伤中的保护效应。将40只大白兔随机平均分为4组:对照组、I/R组、C—IP组和NWIP组。对比观察各组血清及肺组织中NO2^-/NO3^-、丙二醛(MDA)含量及超氧化物歧化酶(SOD)活性以及肺湿/干重比。结果N—WIP组和C-IP组的兔肺再灌注后NO2^-/NO3^-含量均高于I/R组(P〈0.01),甚至高于对照组(P〈0.05)。两种缺血预处理组SOD活性均高于I/R组(P〈0.01),肺湿/干重比和MDA含量均低于I/R组(P〈0.05,P〈0.01)。结论N-WIP与C-IP对移植肺在缺血/再灌注损伤中具有同等强度的保护作用。其机制可能是通过诱发内源性一氧化氮(NO)舒张血管,从而起到保护血管内皮的效应。

关 键 词:缺血预处理  再灌注损伤    一氧化氮
收稿时间:2005-04-26
修稿时间:2005-04-26

Protective effects of endothelia-derived nitric oxide on rabbit lung ischemia/reperfusion injury in non-traumatic ischemic preconditioning
ILYAR Shey-hidin, LUO Dong-bo, CHEN Xue-hong, et al.Protective effects of endothelia-derived nitric oxide on rabbit lung ischemia/reperfusion injury in non-traumatic ischemic preconditioning[J].Chinese Journal of Organ Transplantation,2006,27(2):102-104.
Authors:ILYAR Shey-hidin  LUO Dong-bo  CHEN Xue-hong  
Institution:Department of Thoracic Surgery, The First Affiliated Hospital, Xinjiang Medical University, Urumqi 830054, China
Abstract:Objective To investigate the protective effect of endothelia-derived nitric oxide(NO) on donor lung ischemia/reperfusion (I/R) injury in non-traumatic ischemic preconditioning(N-WIP) and the possible mechanism.Methods Two animal models of N-WIP and classical ischemic preconditioning(C-IP) were used and the protective effects of endothelia-derived NO on rabbit lung I/R injury were compared in those two IP methods.Forty New Zealand White rabbits were randomly divided into 4 groups(n=10 each): control group(C),I/R group,C-IP group,and N-WIP group.Lung injury was assessed by activities of superoxide dismutase (SOD),level of NO~-_2/NO~-_3 and malondialdehyde(MDA) and wet to dry weight ratio(W/D) in serum and lung tissues.Results The content of NO~-_2/NO~-_3 in serum and lung tissues in N-WIP group and C-IP group were both significantly higher than those in I/R group(P<(0.01)),even higher than in group C(P<(0.05)). The activity of SOD in two IP groups were both significantly higher than in I/R group(P<(0.01)). W/D and the levels of MDA in N-WIP group and C-IP group were significantly lower than in I/R group(P<(0.05),P<(0.01)).Conclusions Both N-WIP of hind limbs and C-IP of lung may have a similar protective effect against lung I/R injury. The mechanism may be related to pulmonary arterial endothelia-derived NO induced pulmonary artery relaxation to protect pulmonary vascular endothelial cells.
Keywords:Ischemic preconditioning  Reperfusion injury  Lung  Nitric oxide
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