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机构地区:[1]齐鲁师范学院生物系,山东济南250013 [2]山东中医药大学基础医学院,山东济南250355 [3]山东省农业科学院可持续发展研究所,山东济南250100
出 处:《山东教育学院学报》2010年第6期39-42,共4页Journal of Shandong Education Institute
摘 要:目的:观察戊四氮(PTZ)致痫大鼠海马神经元caspase-3表达以及中药复方AAP的脑保护作用.方法:144只健康成年雄性Wistar大鼠随机分为对照组(CK组)、模型组(PTZ组)、中药大剂量组(AAPl组)、中药中剂量组(AAPm组)、中药小剂量组(AAPs组)和丙戊酸钠组(VPA组);每组各6只.CK组和PTZ组分别给予生理盐水(4mL/kg.d)灌胃;中药各组分别给予中药复方大、中、小剂量(10.26g/kg、5.13g/kg、2.56g/kg)灌胃,每天1次;VPA组腹腔注射VPA(20mg/kg.d).造模第一天,除CK组外,其余各组大鼠均腹腔注射戊四氮(PTZ)75mg/kg,观察记录大鼠行为学变化;于致痫后12h、2d、5d、7d相应时间点取材,制备脑标本;免疫组化检测caspase-3表达.结果:致痫后,除CK组外,其余各组海马区caspase-3阳性表达增强;7天,与PTZ组相比,AAPl组、AAPm组和AAPs组海马CA3区caspase-3阳性表达减弱(P<0.05).结论:caspase-3参与致痫大鼠海马神经元凋亡过程;AAP能降低caspase-3表达,减少神经元凋亡,有神经保护作用.objective:To investigate the effect of AAP,a Chinese medicine compound,on the expression of caspase-3 in hippocampus of epileptic rats induced by pentetrazole(PTZ).Methods:114 health mature male Wistar rats were randomly divided into 6 groups(n=6): Control group(CK group),model group(PTZ group),three AAP groups of high,medium and small doses(AAPl group,AAPm group,AAPs group),sodium valproate group(VPA group).Control group and model group by an intragastric administration of distilled water(4mL/kg·d).Three AAP groups by an intragastric administration at doses of 10.26g/kg,5.13g/kg,2.56g/kg respectively.VPA group by an intraperitoneal injection of sodium valproate(20mg/kg·d).For fhe first day of establishment of the models,seizure was induced by intraperitoneal injection with Pentylenetetrazol(75mg/kg)in all groups other than the control group.Behavioral observation was conducted with Yuhas 5-grade assessment during the establishment of the models.The rats were sacrificed,the brain tissues were sampled and sliced at 12h,2d,5d and 7d following seizures;the expression of caspase-3 was determined by immunohistochemistry.Results:Compared to CK group,theexpression of caspase-3 positive neurons in CA3 subfields increased in all groups;Compared to model group,the expression of caspase-3 positive neurons in CA3 subfields decreased in all the three AAP groups(P0.05).Conclusions:caspase-3 may play a role in the neuronal apoptosis in PTZ induced seizures,and AAP can reduce the expression of caspase-3 in hippocampus CA3 region in seizure rats,which indicates that AAP may have protective effect on brain damage induced by seizure.
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