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作 者:赵丹[1] 袁林辉[2] 张静[2] 张平[3] 余鹏[2] 肖凡[2] 胡小玲[1] 胡衍辉[2]
机构地区:[1]江西省肿瘤医院麻醉科,南昌市330000 [2]南昌大学第二附属医院麻醉科 [3]南昌大学第一临床医学院
出 处:《临床麻醉学杂志》2017年第7期688-692,共5页Journal of Clinical Anesthesiology
基 金:江西省卫计委项目(20165284)
摘 要:目的评价七氟醚后处理对大鼠脑缺血-再灌注时氧化应激及炎症反应的影响,以探讨其脑保护机制。方法健康雄性清洁级SD大鼠36只,12~14周龄,体重220~260g,采用随机数字表法分为假手术组(Sham组)、脑缺血-再灌注组(IR组)和脑缺血-再灌注+七氟醚后处理组(SPC组),每组12只。制备大鼠脑缺血-再灌注损伤模型,缺血30min后再灌注24h。Sham组不阻塞大脑中动脉;IR组:建立脑缺血-再灌注损伤模型;SPC组于再灌注即刻给予2.6%七氟醚吸入15min。再灌注末处死各组大鼠,断头取出脑组织。采用Western blot法检测Iba-1和HO-1蛋白含量;并测定脑组织中活性氧(ROS)含量,丙二醛(MDA)、TNF-α、IL-1β浓度和超氧化物歧化酶(SOD)活性。结果 IR组和SPC组脑皮质Iba-1蛋白含量明显高于Sham组(P<0.05),SPC组Iba-1蛋白含量明显低于IR组(P<0.05)。与Sham组比较,IR组和SPC组ROS含量和MDA、TNF-α、IL-1β浓度明显升高,SOD活性和HO-1蛋白含量明显降低(P<0.05)。SPC组ROS含量和MDA、TNF-α、IL-1β浓度明显低于IR组,SPC组SOD活性和HO-1蛋白含量明显高于IR组(P<0.05)。结论七氟醚后处理能抑制脑缺血-再灌注时诱发的小胶质细胞激活,减轻脑组织氧化应激及炎症反应,从而减轻脑缺血-再灌注损伤,发挥其脑保护作用。Objective To investigate the effects of sevoflurane post-conditioning on oxidative stress and inflammatory reaction during rat cerebral ischemia-reperfusion,and to explore its cerebral protective mechanism.Methods Thirty-six health male Sprague-Dawley rats(aged 12-14 weeks,weighing 220-260g)were randomly divided into 3 groups(n=12 each):sham control group(group Sham),cerebral ischemia-reperfusion group(group IR),sevoflurane post-conditioning group(group SPC).Cerebral ischemia-reperfusion model was established,ischemia for 30 min followed by reperfusion 24 h.Rat middle cerebral artery was not occluded in group Sham.Cerebral ischemia-reperfusion model was established in group IR.Group SPC was subjected to 2.6% sevoflurane for 15 min in the beginning of reperfusion.At the end of reperfusion,rats were cut off the head to take out the brain tissue.The expression level of Iba-1and HO-1proteins was measured by western blot.The levels of reactive oxygen species(ROS),malondialdehyde(MDA),TNF-α,IL-1βand the activity of superoxide dismutase(SOD)were evaluated.Results Compared with group Sham,the expression of cerebral cortex Iba-1protein was higher than that in groups IR and SPC(P〈0.05),the expression of Iba-1 protein in group SPC was lower than that in group IR(P〈0.05).Compared with group Sham,the contents of ROS,MDA,TNF-αand IL-1β were increased in groups IR and SPC(P〈0.05),but the activity of SOD and expression of HO-1protein were decreased(P〈0.05).And the contents of ROS,MDA,TNF-αand IL-1β in group SPC were less than those in group IR,the activity of SOD and expression of HO-1protein in group SPC were higher than those in group IR.Conclusion Sevoflurane post-conditioning can mitigate the microglia activation,reduce cerebral oxidative stress and inflammation,thus protect rat cerebral against ischemia reperfusion injury.
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