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作 者:陆姚[1,2] 胡军[1] 张野[1] 董春山 余骏马
机构地区:[1]安徽医科大学第二附属医院麻醉科,安徽合肥230601 [2]安徽医科大学第三附属医院麻醉科,安徽合肥230061
出 处:《中国药理学通报》2013年第12期1707-1710,共4页Chinese Pharmacological Bulletin
基 金:国家自然科学基金课题(No 81100105)
摘 要:目的探讨脊髓中枢阿片受体在远端缺血预处理减轻大鼠心肌缺血/再灌注损伤中的作用。方法建立鞘内置管和心肌缺血/再灌注损伤模型。大鼠随机分为10组,每组6只:对照组(CON组);远端缺血预处理组(RIPC组);NM组(naloxone methiodide,非特异性阿片受体阻断剂,20μg·kg-1)、nor-BNI组(nor-binaltorphimine,κ阿片受体阻断剂,15nmol)、CTOP组(μ阿片受体阻断剂,15 nmol)和NTD组(naltrindole,δ阿片受体阻断剂,15 nmol);NM+RIPC组、nor-BNI+RIPC组、CTOP+RIPC组和NTD+RIPC组。远端缺血预处理是心脏缺血前经3个循环的左侧股动脉缺血5min和再灌注5 min。左冠状动脉缺血30 min,再灌注120min诱导心肌缺血/再灌注损伤。观察指标包括:血流动力学指标;心肌缺血危险区(AAR)、梗死区(IS)的体积、心肌梗死面积以IS/AAR表示。结果与CON组相比,RIPC组、nor-BNI+RIPC组和NTD+RIPC组的IS和IS/AAR均明显下降(P<0.01);与RIPC组比较,NM+RIPC组和CTOP+RIPC组的IS和IS/AAR均明显升高(P<0.01)。各组在各时点的MAP、HR和RPP比较差异无统计学意义(P>0.05)。结论脊髓中枢μ阿片受体可能参与介导远端缺血预处理减轻大鼠心肌缺血/再灌注损伤中的作用,并不涉及κ和δ阿片受体。Aim To investigate the role of spinal cord opioid receptors in the protective effects of remote is- chemic preconditioning against myocardial ischemia- reperfusion injury in rats. Methods Intrathecal cath- eter placement and myocardial ischemia-reperfusion models were established, and rats were randomly as- signed to 10 groups: control group( CON ) , remote is- chemic preconditioning group ( RIPC ); intrathecal naloxone methiodide group( NM, a non-selective opi- oid receptor antagonist, 20 μg· kg^-1) , intrathecal nor-Binahorphimine group( nor-BNI, a κ opioid recep- tor antagonist, 15 nmol), intrathecal CTOP group ( CTOP, a μ opioid receptor antagonist, 15 nmol) , in- trathecal nahrindole group ( NTD, a δ opioid receptor antagonist, 15 nmol), intrathecal 20 μg · kg^-1 NM + RIPC group( NM + RIPC ) , intrathecal 15 nmol nor- BNI + RIPC group ( nor-BNI + RIPC), intrathecal 15 nmol CTOP + RIPC group ( CTOP + RIPC ), and intrath-ecal 15 nmol NTD + RIPC group( NTD + RIPC ). In- dicators to be observed were composed of hemodynamic values, the volume of area at risk(AAR) , infarct size (IS) , and the area of myocardial infarction, demon- strated by 1S/AAR. Results Compared with CON group, the volume of IS and IS/AAR was reduced in RIPC, nor-BNI + RIPC and NTD + RIPC group (P 〈 0.01 ) ; the protective effects of RIPC was abolished by pretreatment with NM and CTOP (P 〈 0.01 ). There was no significant statistical difference in other observed data among all groups. Conclusion opioid receptor of spinal cord is probablely involved in the protective effects of remote ischemic preconditioning a- gainst myocardial ischemia-reperfusion injury.
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