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机构地区:[1]山西医科大学 [2]山西医科大学基础医学院老年研究所,山西太原030001
出 处:《中国现代医生》2010年第7期7-8,15,共3页China Modern Doctor
摘 要:目的探讨胰高血糖素样多肽1(GLP-1)对链尿佐菌素(STZ)所诱导的阿尔茨海默病(AD)样大鼠实验动物模型在行为学和病理学的作用。方法将24只大鼠随机平均分成对照组、AD模型组和GLP-1保护组。对照组侧脑室予以注射生理盐水;AD模型组侧脑室注射STZ;GLP-1保护组侧脑室注射STZ+GLP-1。Morris水迷宫检测学习记忆功能。结果Morris水迷宫定位航行实验,AD模型组的逃避潜伏期比对照组和GLP-1保护组的都长,而对照组与GLP-1保护组间的逃避潜伏期无差异;空间探索实验,对照组、AD模型组和GLP-1保护组在原平台象限游泳时间与总时间比分别为(49.00±3.04)%、(28.92±4.08)%、(32.30±4.52)%。结论GLP-1能改善AD模型大鼠的学习记忆功能。Objective To study protective effect of GLP-1 (glucagon-like peptide-1 ) on behavior and pathology in Alzheimer disease(AD) rats induced by streptozocin(STZ ). Methods Twenty-four rats were randomly divided into three groups:control group, AD model group and GLP-1 protection group. The control group received intracerebroventricular injection of saline. The AD model group received intracerebroven- tricular injection of STZ,and the GLP-1 protection group received intracerebroventricular injection of STZ plus GLP-1. The capacity of learn- ing and memory of the rats was detected by Morris water maze. Results In Morris water maze place navigation test, the escape latency of the AD model group was longer than that of the control group and GLP-1 protection group each day(P〈0.05),with no significant difference in the escape latency between the control and GLP-1 protection groups. In the space exploration test,the percentage in the platform quadrant of all the three groups was(49.00±3.04)%, (28.92± 4.08)% and(32.30±4.52)%,respectively. Conclusion GLP-1 can enhance the capacity of learning and memory of the rats induced by STZ in Morris water maze.
分 类 号:R749.16[医药卫生—神经病学与精神病学]
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