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作 者:张燕[1] 王震虹[1] 何振洲[1] 忻纪华[1]
机构地区:[1]上海交通大学医学院附属仁济医院南院麻醉科,上海201112
出 处:《中国医药导报》2015年第31期4-7,12,F0003,共6页China Medical Herald
基 金:国家自然科学基金项目(81300996);上海交通大学医学院科学技术基金资助项目(12XJ10054)
摘 要:目的探讨大鼠前脑缺血再灌注(I/R)损伤后,Kappa阿片受体(KOR)激动剂Salvinorin A(SA)减轻脑水肿的机制。方法成年健康雄性Sprague-Dawley(SD)大鼠随机分为5组(n=10):假手术组、I/R组、DMSO(SA溶剂)组、SA组和Norbinaltorphimine(nor-BIN,KOR拮抗剂)+SA组。夹闭双侧颈动脉联合低血压诱发前脑缺血10 min,在缺血后即刻给予DMSO、SA和nor-BIN+SA。再灌注后24 h处死大鼠,取其海马组织做病理,采用末端转移酶d UTP缺口末端标记(TUNEL)及免疫组织化学检测AQP4蛋白水平,用干-湿重法评估脑含水量。结果与假手术组比较,I/R组海马脑含水量增加(P<0.01);SA组和I/R组相比,海马脑含水量显著下降(P<0.01);nor-BIN+SA组脑含水量显著高于SA组(P<0.05)。前脑缺血再灌注后24 h,与I/R和DMSO组比较,SA组显著减少海马神经细胞坏死和凋亡(P<0.01),而nor-BIN可抵消这一作用。与假手术组比较,海马的AQP4蛋白水平,在I/R组显著增加(P<0.01);与I/R组比较,SA组显著下降(P<0.01);nor-BIN+SA组AQP4的蛋白水平和SA组相比明显增加(P<0.05)。结论 SA可以明显减轻前脑缺血后的脑水肿,减轻脑损伤,抑制AQP4的蛋白水平,其作用可能和KOR相关。Objective To discuss the mechanism of Kappa opioid receptor(KOR) agonist Salvinorin A(SA) on decreasing brain edema after forebrain ischemia-reperfusion(I/R) injury in rats. Methods Male Sprague-Dawley rats were divided into 5 groups(n=10): sham operation group,I/R group,DMSO(vehicle) group,SA group and Norbinaltorphimine(nor-BIN,KOR antagonist) +SA group. Forebrain ischemia was performed by low artery pressure with bilateral carotid artery occlusion for 10 minutes. Intervenes(DMSO,SA,nor-BIN+SA) were performed after forebrain ischemia instantly.The animals were sacrificed 24 hours after reperfusion. The hippocampus was taken for pathology,and Td T-mediated d UTP nick end labeling(TUNEL) and immunohistochemical test were used for AQP4 detection. The wet-dry weight method was used to assess brain water content. Results Compared with sham operation group,hippocampus water content increased in I/R group(P〈 0.01). Hippocampus water content was significantly lower in SA group than that in I/R group(P 〈0.01). Hippocampus water content was significantly higher in nor-BIN+SA group than that in SA group(P〈 0.05). Compared with I/R and DMSO groups,hippocampus neurosis and apoptosis were alleviated significantly with treatment of SA 24 h after forebrain I/R(P〈 0.01),which effect was blunted by nor-BIN. Compared with sham operation group,AQP4 expressed in hippocampus was promoted by I/R(P〈 0.01). Compared with I/R group,AQP4 expressed was depressed in SA group(P〈 0.01). The expression of AQP4 increased significantly with treatment of norBIN+SA compared with SA(P〈 0.05). Conclusion SA can reduce cerebral edema after forebrain ischemia and brain damage by inhibition of AQP4. Its mechanism may be correlated with KOR.
关 键 词:脑缺血再灌注 脑水肿 脑损伤 κ阿片受体激动剂 水通道蛋白4
分 类 号:R743.3[医药卫生—神经病学与精神病学]
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