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作 者:隋海娟[1] 马瑞国 刘佳颖[3] 刘卓[1] 闫恩志[1] 金英[1]
机构地区:[1]辽宁医学院药理学教研室 [2]锦州奥鸿药业有限责任公司 [3]辽宁医学院医疗学院,锦州121001
出 处:《中药药理与临床》2015年第6期27-30,共4页Pharmacology and Clinics of Chinese Materia Medica
基 金:辽宁省科学技术基金项目(2013022008)
摘 要:目的:探讨知母皂苷(SAa B)对Aβ_(1-42)诱导的皮层神经元损伤是否有保护作用。方法:MTT法测皮层神经元细胞存活率;免疫荧光染色法检测神经元突触素(SYP)、突触后致密蛋白95(PSD-95)表达的改变。Western印迹法检测神经元SYP、PSD-95、p-Akt473、p-m TOR蛋白表达水平表达的改变。结果:Aβ_(1-42)作用48 h可使大鼠大脑皮层神经元细胞存活率明显降低,使神经元SYP、PSD-95、p-Akt473和p-m TOR蛋白表达明显降低。SAa B(0.01,0.1,1,5,10μmol/L)可明显对抗Aβ_(1-42)引起的神经元细胞存活率下降,并呈一定浓度依赖性。SAa B也可使SYP、PSD-95、p-Akt473和p-m TOR蛋白表达明显增加。结论:知母皂苷能够抑制Aβ_(1-42)诱导的皮层神经元突触损伤,这种作用可能与PI3K/Akt/m TOR信号转导通路有关。Objective:To investigate whether saponin B can protect cortical neurons from Aβ1-42 induced synaptic damage. Methods: The cell via- bility was assessed by MTT assay. Immunstaining were used for SYP and PSD-95 protein expression. The protein expression of SYP, PSD- 95, p-Akt473 and p-mTOR were determined by Western blotting. Results: The decrease of cell viability and the decrease of SYP, PSD-95, p-Akt473 and p-mTOR protein in cultured cortical neurons were observed incubated with A13142 for 48 h compared with the normal controls. SAaB (0.01, 0.1, 1, 5, 10 βmoL/L) inhibited Aβ1-42-induced decrease in cell viability, and showed a dose-dependent. SAaB induced the increases of SYP, PSD-95, p-Akt473 and p-roTOR protein expression. Conclusion:SAaB can inhibited the Aβ1-42-induced synaptic damage in cultured cortical neurons, which mainly via activated P13K/Akt/mTOR signal pathway.
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