孔令娜, 耿美玉, 牟亮, 辛现良, 杨楠, 左萍萍. 酸性寡糖对阿尔茨海默病模型小鼠脑内基因表达的影响J. 药学学报, 2005, 40(12): 1105-1109.
引用本文: 孔令娜, 耿美玉, 牟亮, 辛现良, 杨楠, 左萍萍. 酸性寡糖对阿尔茨海默病模型小鼠脑内基因表达的影响J. 药学学报, 2005, 40(12): 1105-1109.
KONG Ling-na, GENG Mei-yu, MU Liang, XIN Xian-liang, YANG Nan, ZUO Ping-ping. Effects of acidic oligose on differentially expressed genes in the mice model of Alzheimer’s disease by microarrayJ. Acta Pharmaceutica Sinica, 2005, 40(12): 1105-1109.
Citation: KONG Ling-na, GENG Mei-yu, MU Liang, XIN Xian-liang, YANG Nan, ZUO Ping-ping. Effects of acidic oligose on differentially expressed genes in the mice model of Alzheimer’s disease by microarrayJ. Acta Pharmaceutica Sinica, 2005, 40(12): 1105-1109.

酸性寡糖对阿尔茨海默病模型小鼠脑内基因表达的影响

Effects of acidic oligose on differentially expressed genes in the mice model of Alzheimer’s disease by microarray

  • 摘要: 目的应用基因芯片检测酸性寡糖971对阿尔茨海默病(AD)模型小鼠脑内基因表达谱的影响。方法 Balb/c小鼠随机分为对照组、AD模型组(β-AP25-35侧脑室注射)和971给药组,采用Morris水迷宫测试小鼠行为学改变;提取各组小鼠大脑皮层总RNA,与含有1 176个基因的cDNA表达谱芯片进行杂交。并用RT-PCR对其中5个基因表达进行验证。结果AD模型组寻找平台潜伏期比对照组显著延长,给予971可使其明显缩短。基因芯片结果显示,模型组与对照组存在表达差异的基因共有31个,其中上调19个,下调12个;给药组与模型组存在表达差异的基因共有17个,其中上调13个,下调4个。RT-PCR结果显示基因变化趋势与芯片结果相符。结论酸性寡糖971改善AD模型小鼠学习记忆功能可能与DNA损伤修复、神经生长、突触可塑性、免疫应答等相关基因的表达变化有一定关系。

     

    Abstract: AimTo investigate the molecular mechanism of protective effect of acidic oligose 971 on Alzheimer’s disease mouse model by using microarray. MethodsBalb/c mice were randomly divided into control group, β-AP25-35 icv injected group and 971-treated group. The learning-memory ability of mice was tested by Morris water maze experiment. Total RNA of the cerebral cortex was extracted from the mice of each group. cDNA microarrays containing 1 176 genes were used to investigate the gene expression pattern of each group. Expressions of 5 genes were randomly selected for further confirmation by RT-PCR. ResultsIcv injection of β-AP25-35 caused significant impairments in spatial and working memory performances of mice in Morris water maze and which were relieved by the treatment of 971. Up- and down- regulated genes were 19 and 12 in β-AP25-35-injected group vs control group, respectively. Up- and down- regulated genes were 13 and 4, respectively, in 971-treated group vsβ-AP25-35-injected group. RT-PCR results indicated that 5 genes showed identical results to that of the microarray. ConclusionThe protective effect of 971 on learning and memory ability of β-AP25-35-treated mouse may be related to the expression changes of genes involved in cell cycle, DNA repair, nerve growth, synaptic plasticity and immune response, etc.

     

/

返回文章
返回