摘要
目的:研究β-淀粉样蛋白1-42(Aβ1-42)寡聚体诱导痴呆大鼠脑海马区的Bcl-2表达和caspase-3活性变化及其意义.方法:采用Morris水迷宫法筛选出逃避潜伏期少于60 s的60只SD雄性大鼠随机分为4组,即正常对照组、PBS对照组、Aβ1-42纤维组、Aβ1-42寡聚体组.通过脑立体定位仪将Aβ1-42纤维体、Aβ1-42寡聚体注入大鼠右侧脑室,制备AD大鼠模型.RT-PCR法检测大鼠海马Bcl-2 mRNA、caspase-3 mRNA的表达,用免疫印迹测定大鼠海马区Bcl-2蛋白表达和caspase-3活性.结果:与正常对照组及PBS对照组比较,模型组大鼠海马区Bcl-2 mRNA和Bcl-2蛋白表达较低,Aβ1-42纤维组Bcl-2的蛋白表达高于Aβ1-42寡聚体组;Aβ1-42寡聚体组的caspase-3 mRNA表达以及caspase-3蛋白活性高于Aβ1-42纤维组.结论:Aβ1-42寡聚体可下调Bcl-2表达,活化caspase-3.
Objective: To study the expression of Bcl-2 and the activation of caspase-3 of the hippocampus in Alzheimer's disease (AD) rat model induced by Aβ1-42 oligomer and its significance. Methods: Morris water maze method was used to screen the experimental animal. 60 rats (the escape latency less than 60 s) were randomly divided into four groups (n= 15) : a normal group, a PBS control group, Aβ1-42 fiber group and Aβ1-42 oligomers group. The Aβ1-42 fiber body and Aβ1-42 oligomers were injected into rat right cerebral ventricle for preparation AD rat model; PBS control group injected with PBS; normal group without any treatment. RT-PCR method was used to detect the expression of Bcl-2 mRNA and caspase-3 mRNA of the hippocampus in AD rats, and Western blotting assay was used to detect Bcl-2 protein expression and activity of caspase-3 protein in the rat hippocampus. Results: Compared with the normal group and PBS control group, the expression levels of Bcl-2 mRNA and Bcl-2 protein in the hippocampus was down-regulated in the model group rats, the expression level of Bcl-2 protein was higher in Aβ1-42 fiber group than in Aβ1-42 oligomers group; the expression of caspase-3 mRNA and the activity of caspase-3 protein in Aβ1-42 oligomers group was increased compared with the Aβ1-42 fiber group. Conclusion: Aβ1-42 oligomers can reduce Bcl-2 protein expression, and increase the activity of caspase-3 protein.
出处
《解剖学杂志》
CAS
CSCD
北大核心
2014年第2期181-184,共4页
Chinese Journal of Anatomy
基金
国家自然科学基金(81260174)
2012年广西硕士研究生科研创新项目(YCSW2012108)