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CIB1沉默表达对大鼠脑缺血-再灌注损伤后Caspase-3 mRNA表达影响
引用本文:吴日乐,贾锋,冯勇,王宇,江基尧,殷玉华.CIB1沉默表达对大鼠脑缺血-再灌注损伤后Caspase-3 mRNA表达影响[J].昆明医学院学报,2010,31(10):7-11.
作者姓名:吴日乐  贾锋  冯勇  王宇  江基尧  殷玉华
作者单位:[1]内蒙古自治区医院神经外科,内蒙古呼和浩特010010 [2]上海交通大学附属仁济医院神经外科,上海200127
基金项目:2008年上海市基础研究重点资助项目
摘    要:目的探讨钙离子结合蛋白(calcium and integrin-binding protein,CIB1)双链RNA(CIB1.siRNA)对大鼠脑缺血-再灌注损伤的作用.方法 SD大鼠120只,随机分成三组(每组40只):假手术组(S组)、局灶性脑缺血-再灌注组(A组)、局灶性脑缺血-再灌注+CIB1-siRNA组(B组).A组、B组行大脑中动脉阻断,阻断1 h再开放,制备大鼠局灶性脑缺血-再灌注模型,B组在缺血前即刻、16、24 h水压法尾静脉注射CIB1-siRNA 2.5 mg/kg(用PBS稀释至10 mL),S组给予等量PBS,S组只作切口,不作缺血再灌注.S组、B组、A组分别于再灌注1、5、11、23、47 h各处死8只大鼠,断头取脑,计算脑梗塞体积比,用RT-PCR法测定脑缺血半影区Caspase-3 mRNA表达水平.结果 B组、A组再灌注23 h时脑梗塞体积比达到高峰,再灌注47 h脑梗塞体积比均高于S组(P〈0.01);与A组比较,B组脑梗塞体积比增加(P〈0.01).A组和B组再灌注5 h时Caspase-3 mRNA表达高峰,B组各时间段Caspase-3 mRNA表达均强于A组.结论 CIB1-siRNA预先给药可加重大鼠脑缺血再灌注损伤.

关 键 词:CIB1沉默  大鼠  缺血-再灌注损伤

Effect of CIB1 Silence on the Expression of Caspase-3 in Brain Tissues of Rats with Brain Ischemia-reperfuslon Injury
WU Ri-le,JIA Feng,FENG Yong,WANG Yu,JIANG Ji-yao,YIN Yu-hua.Effect of CIB1 Silence on the Expression of Caspase-3 in Brain Tissues of Rats with Brain Ischemia-reperfuslon Injury[J].Journal of Kunming Medical College,2010,31(10):7-11.
Authors:WU Ri-le  JIA Feng  FENG Yong  WANG Yu  JIANG Ji-yao  YIN Yu-hua
Institution:1.Dept.of Neurosurgery,The People's Hospital of Inner Mongolia Autonomous Region,Hohhot Inner Mongolia 010010;2.Dept.of Neurosurgery,Shanghai Renji Hospital,School of Medicine,Shanghai Jiaotong University,Shanghai 200127,China)
Abstract:Objective To investigate the protective effect of CIB1-siRNA pretreatment on the brain against ischemia-reperfusion in rats.Methods 120 male SD rats weighing 290~310 g were randomly divided into 3 groups:sham operation group(S group,n=40);middle cerebral artery occlusion group(MCAO)(A group,n=40)and CIB1-siRNA +MCAO group(B group,n=40).The middle cerebral arteries of rats in A group and B group were blocked,MCAO was maintained for 1 h and the nylon thread was withdrawn to allow reperfusion.In B group,CIB1-siRNA solution(2.5 mg/kg)was given i.v.immediately before MCAO,at 24 h and 16 h after MCAO.In S group,the internal carotid artery was exposed but no MCAO was performed,and PBS solution was given instead of CIB1-siRNA solution.The animals in all groups were killed at 1,5,11,23 and 47 h after reperfusion(n=8 at each time point).Brains were immediately removed and sliced.The infarct size was estimated by using Kontron IBAS 2.5 image auto-analysis system.The Caspase-3 mRNA expression was measured by RT-PCR.Results The infarct size of rats in A group and B group reached the peak at 23 h after reperfusion,and was significantly bigger than that in S group at 47 h after reperfusion(P〈0.01).The infarct size of rats in B group was significantly bigger than that in A group(P〈0.01).The expression of Caspase-3 protein in A group and B group reached the peak at 23 h after reperfusion.The expression levels of Caspase-3 protein in B group was higher than that in A group.Conclusion CIB1-siRNA pretreatment can aggravate the brain I/R injury to some extent.
Keywords:CIBI silenc  Rat  Ischemia-reperfusion injury
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