摘要
目的:观察重组人血小板活化因子乙酰水解酶(rPAF-AH)对阿尔茨海默病(Alzheimer's disease,AD)小鼠认知功能的改善。方法:取昆明小鼠80只,分为正常对照组、模型对照组、rPAF-AH用药组和金纳多治疗组(每组20只),通过海马注射B.淀粉样蛋白(β-amyloid protein,AB)制备出AD小鼠模型,尾静脉注射rPAF-AH 7 d后观测AD小鼠水迷宫神经行为学的改变。采用Westem blotting研究小鼠大脑海马AB的表达及活性,同时与金纳多注射液及假手术对照组比较。结果:水迷宫试验显示,rPAF-AH处理组小鼠60s内跨越平台的次数和在目标象限的探索时间均明显增加(P<0.01)。western blotting结果显示,rPAF-AH处理可降低小鼠大脑海马AB的表达及活性水平(P<0.05)。结论:重组人PAF-AH处理对AD小鼠有一定的保护作用,这可能得益于其抑制了Aβ蛋白的高表达。
Objective:To study the effects of recombinant human platelet-activating factor acetylhydrolase (rPAF-AH) on improving cognition in mice with Alzheimer's disease (AD). Methods: A total of 80 Kunming mice were allocated to normal control group (n = 20), model control group (n = 20), rPAF-AH group (n = 20) and Ginaton group ( n = 20) , respectively. The AD model was established via hippocampal injection of [5-amyloid protein in mice. This was followed by obsetvation of behavioral changes in the water maze test at day 7 after injection with rPAF-AH. Western blotting was employed to determine the hippocampus AI3 protein expression and activity, which allowed comparison with Ginaton group and model control group. Results: The results of Morris water maze test showed that rPAF-AH markedly increased the number of movement across the platform in 60 s and the duration for exploring in the target quadrant ( both P 〈0. 05 ). Western blotting indicated that rPAF-AH reduced A[3 expression and activity ( both P 〈 0.05 ). Conclusion : The treatment with rPAF-AH that protects from injury of AD in mice could be attributed to suppression of A~ expression.
出处
《广州医学院学报》
2013年第4期18-21,共4页
Academic Journal of Guangzhou Medical College
基金
广州医学院博士启动资助项目(编号:2012C29)
广州市卫生局医药卫生科技项目(编号:2013A010025)