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机构地区:[1]重庆医科大学神经科学中心 [2]重庆医科大学基础医学院人体解剖学教研室,重庆400016
出 处:《重庆医科大学学报》2015年第5期662-665,共4页Journal of Chongqing Medical University
基 金:国家自然科学基金资助项目(编号:30970986、81371221);教育部“新世纪优秀人才支持计划”资助项目(编号:NCET-11-1084)
摘 要:目的:观察丙戊酸钠(valproic acid sodium salt,VPA)对阿尔茨海默病(Alzheimer’s disease,AD)模型小鼠脑内星形胶质细胞、脑源性神经营养因子(brain-derived neurotrophic factor,BDNF)和胶质细胞源性神经营养因子(glial cell line-derived neurotrophic factor,GDNF)的影响。方法:取3月龄的APP/PS1双转基因小鼠AD模型小鼠24只,按随机数字表法平均分为治疗组和对照组。VPA治疗组小鼠腹腔注射VPA 30 mg/(kg·d),对照组小鼠腹腔注射等量生理盐水,采用免疫组化学法观察2组小鼠皮质和海马区星形胶质细胞数量的变化,Western blot检测2组小鼠皮质和海马BDNF和GDNF的表达水平。结果:与对照组比较,VPA治疗组小鼠皮质和海马区星形胶质细胞标志物胶质纤维酸性蛋白(glial fibrillary acidic protein,GFAP)的阳性细胞数量均明显减少(t=5.476、8.793,P均=0.000),BDNF和GDNF表达水平均明显升高(t=4.303,P=0.001;t=2.376,P=0.032)。结论:VPA可抑制星形胶质细胞增生,提高神经营养因子的表达水平。Objective:To investigate the effect of valproic acid sodium salt(VPA)on astrocyte and neurotrophic factors in the brain of APP/PS1 double transgenic mice. Methods:Alzheimer's disease(AD)model was established with APP/PS1 double transgenic mice.Twenty-four mice(3-month-old)were randomly divided into a VPA group and a control group. The mice of VPA group and control group were intra peritoneally injected with VPA 30 mg/(kg·d)and the same amount of normal saline for 4 weeks. Immunohistochemistry staining was applied to detect the number of astrocytes,while Western blot was used to observe the expression of brain-derived neurotrophic factor(BDNF) and glial cell line-derived neurotrophic factor(GDNF). Results:Compared with those of control group,the number of positive cells of the astrocyte marker glial fibrillary acidic protein(GFAP)in the cortex and hippocampus of VPA treatment mice was significantly reduced(t=5.476,8.793,P〈0.001)and the expression levels of BDNF and GDNF were significantly increased(t=4.303,P=0.001;t=2.376,P=0.032). Conclusion:VPA can inhibit the proliferation of astrocytes,enhance the expression of neurotrophic factors.
关 键 词:阿尔茨海默病 丙戊酸钠 星形胶质细胞 神经营养因子
分 类 号:R394.3[医药卫生—医学遗传学] R741.05[医药卫生—基础医学]
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