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机构地区:[1]贵州医科大学附院病理科,贵州贵阳550004 [2]贵州医科大学地方病与少数民族性疾病教育部重点实验室,贵州贵阳550004
出 处:《贵州医科大学学报》2016年第12期1376-1381,共6页Journal of Guizhou Medical University
基 金:国家自然科学基金(81260173);教育部"长江学者和创新团队发展计划资助"(IRT13058);贵州省科技计划[黔科合重大专项字(2014)6008号];贵州省创新计划项目[黔教合协同创新中心(2014)06]
摘 要:目的:探讨β-淀粉样蛋白(Aβ)对原代培养海马神经细胞中沉默信息调节因子(SIRTs)表达的影响。方法:分离出生24 h内SD乳鼠大脑海马区域,培养原代神经细胞,CCK-8试验观察0、0.1、0.2、0.5、1.0、1.5及2.0μmol/L Aβ寡聚体(AβOs)对细胞增殖的影响,选取恰当浓度的AβOs进行后续实验;将实验分为对照组(Control)和Aβ组,Aβ组给AβOs处理24 h后,运用Western blotting方法及Realtime PCR方法检测SIRT1、SIRT3、SIRT4及SIRT5的蛋白及mRNA表达水平。结果:CCK-8结果显示,0.5μmol/L AβOs作用于大鼠原代海马神经细胞24 h时细胞存活率明显低于对照组(P<0.05),且不影响细胞的存活率;0.5μmol/L AβOs处理大鼠原代海马神经细胞24 h后,与Control相比,SIRT1、SIRT3、SIRT4及SIRT5蛋白及mRNA表达水平均不同程度降低(P<0.05或0.01)。结论:AβOs可使海马神经细胞中SIRTs蛋白及mRNA表达水平降低,这可能与AD病人发病后学习记忆能力减退有关。Objective: To investigate the effect of β-amyloid peptide (Aβ) on expressions of silent information regulators (SIRTs) in rat primary hippocampal neurons. Methods: Rat primary neurons were prepared and cultured from the brain hippocampus of newborn (within 24 h) SD rats. Cell Counting Kit-8 (CCK-8) was employed to detect the effect of 0, 0.1, 0.2, 0.5, 1.0, 1.5 and 2. 0 p.moL/ L Aβ oligomers (AβOs) on proliferation of neurons. The appropriate concentration of A βOs was select- ed for subsequent experiments. Rat primary hippoeampal neurons were divided into control group and A β group which was treated with A β for 24 h. The protein and mRNA expressions of SIRT1, SIRT3, SIRT4 and SIRT5 were detected by Western blotting and real-time PCR. Results: According to CCK- 8 results, 0. 5 μmol/L AβOs was selected for subsequent experiments. The protein and mRNA expres- sion of SIRT1, SIRT3, SIRT4 and SIRT5 were significantly attenuated when the cells treated with 0.5 μmol/L AβOs for 24 h. Conclusions: AβOs can reduce the levels of protein and mRNA of SIRTs in rat primary hippocampal neurons, which might be a mechanism of cognitive deficit of AD.
关 键 词:阿尔茨海默病 β-淀粉样肽1-42 海马神经元 沉默信息调节因子
分 类 号:R749.1[医药卫生—神经病学与精神病学] R34-33[医药卫生—临床医学]
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