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作 者:杜红蕾[1] 宋春雨[1] 王泽宇[2] 魏春杰[2] 韩凤[2] 杨晓玉[2] 盛宝英[2]
机构地区:[1]佳木斯大学,黑龙江佳木斯154002 [2]佳木斯大学附属第一医院神经内科,黑龙江佳木斯154002
出 处:《现代生物医学进展》2015年第21期4020-4024,共5页Progress in Modern Biomedicine
基 金:黑龙江省教育厅科学技术研究项目(12531698);黑龙江省高校科技创新团队项目(2012TD013);佳木斯大学研究生创新基金(LZR2014_018)
摘 要:目的:观察神经干细胞对AD大鼠海马周围微环境中SNAP-25表达及其认知功能的影响。方法:取成年雄性Wistar大鼠30只,随机分为对照组、AD模型组、细胞移植组,每组10只。采用凝聚态Aβ1-42注射到大鼠海马组织内建立阿尔茨海默病(AD)大鼠动物模型,通过Y迷宫测试大鼠学习记忆能力和Western blot技术检测大鼠海马组织内SNAP-25的表达。结果:Y迷宫测试结果显示术后4周时AD模型组和细胞移植组大鼠学习记忆均低于对照组,与AD模型组比较,细胞移植组大鼠学习记忆能力明显高于AD模型组,差异有统计学意义(P<0.05);Western blot检测结果显示术后4周时AD模型组和细胞移植组大鼠海马组织内SNAP-25蛋白表达量均低于对照组,与AD模型组比较,细胞移植组大鼠海马组织SNAP-25蛋白表达量高于AD模型组差异有统计学意义(P<0.05)。结论:移植的NSCs可改善AD大鼠的学习和记忆能力,其机制可能是通过改变海马区周围的微环境并上调了海马组织内SNAP-25表达。Objective: To investigate the effects of neural stem cells in rat hippocampal AD surrounding microenvironment SNAP-25 expression and cognitive function. Methods: 30 Adult male Wistar rats were randomly divided into control group, AD model group, cell transplantation groups of 10. Aβ1-42 injection to establish the use of condensed matter senile dementia (AD) in the hip- pocampus of rats rat model of learning and memory in rats by Y-maze test, SNAP-25 expression within the Western blot technique rat hippocampus. Results: Y maze test results show after 4 weeks when AD model group and cell transplantation group learning and memo- ry in rats were lower than the control group, compared with the AD model group, cell transplantation group learning and memory abili- ties of rats was significantly higher than AD model group, the difference statistically significant (P〈0.05); Western blot test results show after 4 weeks AD model group and cell transplantation in the rat hippocampus SNAP-25 protein expression levels than the control group, compared with the AD model group, cell transplanted rat SNAP-25 protein expression in hippocampal tissues than AD model group, the difference was statistically significant (P〈0.05). Conclusion: Transplanted neural stem cells can improve learning and memory in AD rats, and its mechanism may be by altering the microenvironment surrounding the hippocampus and raised the SNAP 25- expression within the hippocampus.
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