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七氟醚预处理对局灶性脑缺血再灌注损伤大鼠海马TREK-1表达的影响
引用本文:周俊,姚尚龙,杨承祥,仲吉英,高润兴,李云.七氟醚预处理对局灶性脑缺血再灌注损伤大鼠海马TREK-1表达的影响[J].中华麻醉学杂志,2010,30(4).
作者姓名:周俊  姚尚龙  杨承祥  仲吉英  高润兴  李云
作者单位:1. 佛山市第一人民医院麻醉科,528000
2. 华中科技大学同济医学院附属协和医院麻醉科,武汉市,430022
摘    要:目的 探讨七氟醚预处理对局灶性脑缺血再灌注损伤大鼠海马机械敏感性钾通道TREK-1表达的影响.方法 健康雄性SD大鼠36只,体重240~280 g,随机分为3组(n=12):假手术组(S组)、局灶性脑缺血再灌注组(l/R组)和七氟醚预处理组(Sevo组).结扎右侧颈总动脉、颈外动脉,采用线栓法阻断颈内动脉2 h,再灌注24 h制备大鼠局灶性脑缺血再灌注损伤模型;Sevo组于缺血前1 h经半密闭的吸入箱持续吸入含2.5%七氟醚的02;S组仅分离并结扎右侧颈总动脉、颈外动脉,不置入线栓.各组于再灌注24 h时行神经功能缺陷评分后断头取脑,TIC染色后测定脑梗死体积,采用RT-PCR法测定海马TREK-1 mRNA的表达.结果 与S组相比,I/R组和Sevo组神经功能缺陷评分和脑梗死体积比升高(P<0.01);与I/R组相比,Sevo组神经功能缺陷评分和脑梗死体积比降低,海马TREK-1 mRNA表达上调(P<0.05).结论 七氟醚预处理可通过激活海马TREK-1减轻大鼠局灶性脑缺血再灌注损伤.

关 键 词:麻醉药  吸入  缺血预处理  梗死  大脑中动脉  钾通道  双孔  海马

Effect of sevoflurane preconditioning on TREK-1 channel expression in hippocampus after focal cerebral ischemia-reperfusion in rats
ZHOU Jun,YAO Shang-long,YANG Cheng-xiang,ZHONG Ji-ying,GAO Run-xing,LI Yun.Effect of sevoflurane preconditioning on TREK-1 channel expression in hippocampus after focal cerebral ischemia-reperfusion in rats[J].Chinese Journal of Anesthesilolgy,2010,30(4).
Authors:ZHOU Jun  YAO Shang-long  YANG Cheng-xiang  ZHONG Ji-ying  GAO Run-xing  LI Yun
Abstract:Objective To investigate the effect of sevoflurane preconditioning on TREK-1 channel expression in hippocampus after focal cerebral ischemia-reperfusion (I/R)in rats and the mechanism.Methods Thirty-six male SD rats weighing 240-280 g were randomly divided into 3 groups(n=12 each):group Ⅰ sham operation (group S),group Ⅱ I/R and group Ⅲ sevoflurane preconditioning (group Sevo).Focal cerebral ischemia was produced by inserting a 4-0 nylon thread with rounded tip into right internal jugular vein.The nylon thread was the nylon thread Wag about 18-20 Innl.The right middle cerebral artery(MCA)Wag occluded for 2 h and then released for 24 h reperfusion.The Sevo group inhaled 2.4% sevoflurane for 30 min at l h before ischemia.Neurological deftcits were assessed and scored at the end of 24 h reperfusion (the higher was the score,the severer was the deficit).The cerebral infarct size was determined by TTC staining and the TREK-1 mRNA in hippocampus by RT-PCR.Results The cerebral infarct size was significantly smaller and the neurological deficit scores were significantly lower in Sevo group than in I/R group.The TREK-1 mBNA expression was significantly up-regulated in Sevo group as compared with I/R group.Conclusion Sevoflurane preconditioning Can protect the brain against I/R injury by activating TREK-1 in hippocampus.
Keywords:Inhalation anesthetics  Ischemic preconditioning  Infarction  middle cerebral artery  Potassium channels  tandem pore domain  Hippocampus
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