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作 者:王世玉[1] 崔昕龙[2] 薛富善[2] 刘和平[3] 李瑞萍[2] 刘高谱 杨桂珍[2] 孙超[2] 廖旭[2]
机构地区:[1]卫生部中日友好医院麻醉科,北京100029 [2]中国医学科学院,北京协和医学院整形外科医院麻醉科,100144 [3]新乡医学院第三附属医院麻醉科,453003
出 处:《国际麻醉学与复苏杂志》2016年第12期1057-1062,1067,共7页International Journal of Anesthesiology and Resuscitation
基 金:国家自然科学基金(30972836,81170128);河南省教育厅自然科学研究计划项目基金(2011A320011)
摘 要:目的评估联合应用肢体远隔缺血后处理(remote ischemic postconditioning,RIP)和吗啡后处理能否获得增强的心肌保护作用。方法采用大鼠在体心肌缺血,再灌注损伤(ischemia/reperfusion injury,I/RI)模型,采用随机数字表法将60只大鼠分为6组(每组10只):空白对照组(Sham组)、缺血/再灌注(ischemia/reperfusion,I/R)组(I/R组)、缺血预处理(ischemic preconditioning,IPC)组(IPC组)、肢体RIP组(RIP组)、吗啡后处理组(M组)以及联合应用肢体RIP和吗啡后处理组(M+RIP组)。实验中连续监测心律失常情况,计算缺血期和再灌注早期的心律失常评分,检测血清肌酸激酶同工酶(ereatine kinase MB,CK-MB)和心脏肌钙蛋白I(cardiac troponin I,cTnI)浓度,并采用伊文蓝和氯化三苯基四氮唑(triphenyltetrazolium chloride,TYC)双重染色法测定心肌梗死面积。结果I/R组、IPC组、RIP组、M组和M+RIP组的心肌梗死面积分别是(56.0±9.1)%、(23.9±5.5)%、(40.4±11.1)%、(47.7±9.3)%和(27.2±6.7)%。与I/R组比较,M+RIP组再灌注早期心律失常发生率和心律失常评分、血清CK-MB和cTnI浓度以及心肌梗死面积均明显降低(P〈0.05);这些参数在IPC组和M+RIP组之间差异无统计学意义(P〉O.05)。结论在大鼠在体心肌I/RI模型,联合应用肢体RIP和吗啡后处理可获得增强的心肌保护作用,其心肌保护作用类似于IPC。Objective To determine whether combined morphine and limb remote ischemic postconditioning could provide an enhanced protection against myocardial ischemia/reperfusion injury. Methods Using rat in vivo myocardio ischemia/reperfusion injury(I/RI) model, sixty male SD rats were allocated into six groups(n=10) by random number method: control group (group sham), ischema/reperfusion(I/R) group(group I/R), ischemic preconditioning group(group IPC), remote ischemic postconditioning group(group RIP), morphine postconditioning group (group M), and combined morphine and remote ischemic postconditioning groups (group M+ RIP). Arrhythmias were monitored continuously during the experiment and scored in early I/R period. Serum creatine kinase MB (CK-MB) and cardiac troponin I(cTnI) levels were assayed. The infarction area was determined by Evans blue and triphenyltetrazolium chloride(TYC) staining method. Results The infarction area was (56.0±9.1)%, (23.9±5.5)%, (40.4±11.1)%, (47.7±9.3)% and (27.2±6.7)% in the I/R, IPC, RIP, M and M+RIP groups, respectively. The infarction area, serum CK-MB, cTnI level, incidence and score of arrhythmias during early reperfusion period were significantly reduced in group M+RIP compared to group I/R (P〈0.05), butshowed no significant differences between IPC and M+RIP groups (P〉0.05). Conclusions This experiment demonstrates that combined morphine and limb remote ischemic postconditioning provides an enhanced protection against myocardial I/RI which is comparable to ischemic preconditioning.
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