异丙酚对兔缺血/再灌注损伤心肌半胱天冬酶12的影响
二异丙酚;心肌再灌注损伤;半胱天冬酶12;凋亡,,二异丙酚;心肌再灌注损伤;半胱天冬酶12;凋亡,【摘要】,【关键词】,1材料与方法,2
【摘要】 目的 观察异丙酚对兔缺血/再灌注损伤心肌半胱天冬酶12(caspase12)的影响,从内质网角度探讨异丙酚对减少缺血/再灌注损伤心肌细胞凋亡的机制。方法 健康雄性新西兰大白兔24只,体重2.1~2.3 kg。随机分为假手术组(Sham组)、缺血/再灌注组(I/R组)和异丙酚组(P组)(每组8只)。术中胸膜破裂和死亡者不纳入实验,再按照随机原则在相同条件下予以补齐。实验结束后取左心室缺血/再灌注区心肌组织,免疫组织化学方法检测caspase12、半胱天冬酶3(caspase3),用Motic 6.0图像分析系统进行处理,比较各观测指标平均光密度值(Average optical value AO值);用流式细胞检测技术(flow cytometry,FCM)及DNA原位末端缺口标记法(TUNEL法)检测缺血/再灌注区心肌细胞凋亡。结果 Sham组caspase12、caspase3低表达;FCM检测有少量凋亡早期细胞,TUNEL染色见少量阳性细胞;与Sham组比较,I/R组和P组caspase12、caspase3表达增加(P<0.05),FCM检测和TUNEL染色见凋亡细胞数增加(P<0.05);与I/R组比较,P组Caspase12、Caspase3表达下降(P<0.05),FCM和TUNEL染色见凋亡心肌细胞数减少(P<0.05)。结论 抑制caspase12介导的caspase级联反应性凋亡途径的激活是异丙酚减少缺血/再灌注损伤心肌细胞凋亡的机制之一。【关键词】 二异丙酚;心肌再灌注损伤;半胱天冬酶12;凋亡
The effects of propofol on the caspase cascade reaction induced by caspase12 in myocardial ischemiareperfusion injury
DONG Zhenming,REN Jianjun.
Department of Anesthesiology,The Second Hospital of Hebei Medical University,Shijiazhuang 050000
【Abstract】 Objective To investigate the effect of propofol on the caspase12 in ischemiareperfusion myocardium,to elucidate the protective mechanism of propofol on myocardial tissue underwent ischemiareperfusion in rabbit heart.Methods Twentyfour healthy male white rabbits (4 months of age) weighting 2.1~2.3 kg were randomly divided into sham operation group,ischemiareperfusion group and propofol group.The rabbits were anesthetized with 3% pentobarbital 30 mg/kg,to make the model of ischemiareperfusion injury according to the referent literatures. The propofol (2.5 mg·kg·-1·h-1) was infused through the vein at the edge of ear,then infusing it at the dose of 5 mg·kg-1·h-1 continuesly to the end of experiment.The tissues of ischemiareperfusion region were taken to detect the expression of caspase12,caspase3 by immunohistochemistry and to analyze them with Motic 6.0 image analysis system,and to detect the I/R myocardial apoptosis by flow cytometry and TUNEL staining methods.Results The caspase12 and caspase3 expresses in a low level,a few apoptotic cells were detected by FCM and the TUNEL staining in sham operation group.As compared with that in sham operation group,the expression of caspase12 and caspase3 in I/R group and propofol group were higher (P<0.05);the apoptotic cells detected by FCM and TUNNEL methods were significantly increased,as compared with those of sham operation group (P<0.05).As compared with those of I/R group,the levels of caspase12 and caspase3 in propofol group were lower than that of I/R group,the percentage of apoptotic cells was lower than that of I/R group (P<0.05).Conclusion Propofol can decrease the number of apoptotic cells of the ischemiareperfusion myocardium,inhibit the caspase cascade reaction induced by caspase12,which is one of the protective mechanisms of propofol. ......
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