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作 者:郝莉[1] 徐玉英[1] 任秀花[2] 张志雄[3] 高崎 顾慧芬
机构地区:[1]河南中医学院基础医学院,郑州450052 [2]郑州大学基础医学院,郑州450001 [3]上海中医药大学基础医学院,上海201203 [4]上海杏灵科技药业有限公司,上海200127
出 处:《中药药理与临床》2015年第3期96-100,共5页Pharmacology and Clinics of Chinese Materia Medica
基 金:上海市科委科研计划项目资助(项目批准号09ZR1432100);河南中医学院科研苗圃项目资助(MP2012-03)
摘 要:目的:探讨银杏酮酯(Ginkgo biloba extract,GBE50)对自然衰老大鼠学习记忆及海马、前额叶皮层c-fos、Caspase-3和Caspase-8表达的影响。方法:21月龄大鼠随机分为模型组、银杏酮酯组和阳性药银杏叶提取物组,1月龄大鼠作为正常组。其中正常组和模型组用1%羧甲基纤维素钠灌胃,银杏酮酯组和银杏叶提取物组分别予100 mg/kg的药物灌胃60天。新物体识别实验检测学习记忆,免疫组织化学方法检测海马CA1区和前额叶皮层c-fos和Caspase-8的蛋白水平,免疫印迹方法检测海马和前额叶皮层Caspase-3蛋白表达。结果:新物体识别实验结果显示:与模型组相比,100mg/kg银杏酮酯和银杏叶提取物可使大鼠的分辨指数和优先指数明显升高。免疫组织化学结果显示:与模型组相比,100mg/kg银杏酮酯和银杏叶提取物可使海马CA1区和前额叶皮层cfos表达增加,Caspase-8表达降低。免疫印迹结果显示:与模型组相比,100mg/kg银杏酮酯和银杏叶提取物组可使海马和前额叶皮层Caspase-3蛋白表达下降。结论:100mg/kg的银杏酮酯可以改善自然衰老大鼠学习记忆缺陷,这种改善可能与上调自然衰老大鼠海马和前额叶皮层c-fos表达,降低Caspase-3和Caspase-8蛋白水平有关。Objective: To investigate effects of Ginkgo biloba extract (GBES0)on learning and memory in natural aging rats, and the role of c-fos, Caspase-3 and Caspase-8 in the hippocampal and prefrontal cortex. Method: 21-month-old rats were randomly divided into three groups: model group, GBES0 group and positive control(extract of Ginkgo biloba, EGB761 )group, 1 month rats were as normal group. The rats in GBE50 and EGB761 groups received 100 mg/kg GBES0 and EGB761 respectively. The rats in the normal and model groups received solvent ( 1% CMC-Na + ) by intragastric administration for 60 days. Novel object recognition task (NORT) was used to measure learning and memo- ~y; Imunohistochemical staining was used to test e-fos, Caspase-3 and Caspase-8 in the hippocampal and prefrontal cortex. Results: NORT result showed that compared with the model group, the discrimination index and the priority index also increased significantly in the GBE50 and EGB761 groups (P 〈 0, 05 ). Imunohistochemical staining result showed that e-los increased and Caspase-8 decreased respectively in the hippocampal CA1 and prefrontal cortex after GBE50 and EGB761 (100mg/kg) treatment for 60 days ( P 〈 0. 05 ). Western blot displayed that compared with the model group, Caspase-3 and Caspase-8 decreased in the hippocampal and prefrontal cortex after GBE50 and EGB761 (100mg/kg) treatment for 60 days ( P 〈 0.05 ). Conclusion: 100mg/kg GBE50 might improve age-dependent learning and memory deficit, and this might related to the increased expression of c-fos and the decreased expression of Caspase-3 and Caspase-8 in the hippoeampal and prefrontal cortex.
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