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Effects of bone morphogenetic protein-4 on spatial memory and cholinergic expression in the dentate gyrus after fornix-fimbria transection in rats
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作者 Lei Liu Yilong Xue +3 位作者 Jingkun Pan Yazhuo Hu Yuhong Gao Yun Luo 《Neural Regeneration Research》 SCIE CAS CSCD 2008年第1期1-4,共4页
BACKGROUND: Previous experiments have confirmed bone morphogenetic proteins (BMPs) upregulate cholinergic expression in neurons isolated from the embryonic rat hippocampus and cerebral cortex. Therefore, BMPs could... BACKGROUND: Previous experiments have confirmed bone morphogenetic proteins (BMPs) upregulate cholinergic expression in neurons isolated from the embryonic rat hippocampus and cerebral cortex. Therefore, BMPs could be useful for treating Alzheimer's disease and other neurodegenerative diseases. OBJECTIVE: BMP-4 was infused into the hippocampal dentate gyrus of fomix-fimbria transected rats to test the effects of BMP-4 on cholinergic expression in dentate gyrus neurons, and to observe changes in spatial memory behavior. DESIGN: A randomized controlled animal experiment. SETTING: Department of Neurosurgery and Laboratory for Cell Biology, Institute of Geriatrics, General Hospital of Chinese PLA. MATERIALS: Twenty-seven healthy adult male Sprague Dawley (SD) rats, weighing 250-300 g, were provided by the Laboratory Animal Center of the General Hospital of Chinese PLA. Reagents: BMP-4 (B-2680, Sigma Company) and choline acetyl transferase (CHAT) antibody (AB5042, Chemicon Company) were used in this study. Equipments: a rat stereotaxic instrument (type: SN-2N, Narushige Group, Japan) and Image-prog-plus image analysis software (Media Cybernetics company, USA) were used in this study. The protocol was carried out in accordance with ethical guidelines for the use and care of animals. METHODS: This experiment was performed in the Institute of Geriatrics, General Hospital of Chinese PLA between July 2004 and March 2005. Rats were randomly divided into 4 groups: Alzheimer's disease group (n = 7), normal control group (n = 5), BMP-4-Alzheimer's disease group (n = 8), and model group (n = 7). In the Alzheimer's disease group, the left hippocampal fomix-fimbria of rats was transected to mimic Alzheimer's disease symptoms. In the BMP-4-Alzheimer's disease group, 1 μt L BMP-4 (10 mg/L) was perfused into the left dentate gyrus with a microinjector at 1 μ L/min. In the model group, 1 μ L saline was perfused into the same position by the same method. Twenty-eight days after injection, Morris water maze test was performed in all rats to test spatial memory. Time-to-platform and swim-path length were recorded. Immunohistochemical staining of cholinergic neurons was performed on brain sections containing dentate gyrus. The area covered by ChAT-positive cells was analyzed using an Image-prog-plus image analysis software. MAIN OUTCOME MEASURES: Area covered by ChAT-positive cells in the dentate gyrus. Time-to-platform and swim path-length. RESULTS: Twenty-seven rats were included in the final analysis. In the Alzheimer's disease group, the area covered by ChAT-positive cells was significantly smaller compared with the normal control group (F = 76.03, P 〈 0.01). The area covered by ChAT-positive cells was significantly larger in the BMP-4- Alzheimer's disease group than in the model group (F = 35.17, P 〈 0.05), but significantly smaller than in the normal control group (F = 40.17, P 〈 0.05). Time-to-platform and swim-path length were significantly longer in the Alzheimer's disease group than in the normal control group (F =24.62 and 631.58, respectively, both P 〈 0.05). Time-to-platform and swim-path length were significantly shorter in the BMP4-Alzheimer's disease group compared with the model group (F= 22.06 and 606.89, respectively P 〈 0.05). CONCLUSION: Injection of BMP-4 into the dentate gyrus of Alzheimer's disease model rats alleviates central cholinergic system injury and concomitantly improves spatial memory. 展开更多
关键词 senile dementia bone morphogenetic-protein-4 HIPPOCAMPUS dentate gyrus cholinergicneuron Alzheimer's disease
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慢性脑低灌注对2型糖尿病模型大鼠空间学习记忆能力的影响及胆碱能神经元损伤的机制探讨 被引量:3
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作者 李玉梅 张婷 +2 位作者 肖品品 张潇 付剑亮 《中国临床神经科学》 2013年第6期614-619,共6页
目的探讨2型糖尿病(DM)是否加重慢性脑低灌注(CCH)大鼠胆碱能神经元及空间学习记忆能力损伤。方法SD大鼠24只,随机分为4组(均n=6):①对照组(正常饮食+假手术);②DM组[高脂饮食+链脲佐菌素(STZ)];③CCH组[正常饮食+双... 目的探讨2型糖尿病(DM)是否加重慢性脑低灌注(CCH)大鼠胆碱能神经元及空间学习记忆能力损伤。方法SD大鼠24只,随机分为4组(均n=6):①对照组(正常饮食+假手术);②DM组[高脂饮食+链脲佐菌素(STZ)];③CCH组[正常饮食+双侧颈总动脉永久性结扎(2-VO)];④DM-CCH组(高脂饮食+STZ+2-VO)。采用Morris水迷宫测试各组大鼠学习记忆能力;免疫组化学法检测海马区乙酰胆碱转移酶(CHAT)阳性细胞表达和免疫印迹法检测海马ChAT相对表达量。结果DM+CCH组逃避潜伏期与对照组比较明显延长,第2-4天(P〈0.001)、第5天(P〈0.01);目标象限时『目】百分比明显低干对照组(P〈0.01)、DM组(P〈0.05)和CCH组(尸〈O.05)。DM+CCH组海马区ChAT阳性细胞表达明显减少,ChAT相对表达量较对照组显著减少(P〈0.01)、DM组(P〈0.05)和CCH组(P〈0.05)显著减少。结论DM可加重CCH大鼠的空间学习记忆能力障碍,可能与海马区胆碱能神经元损伤有关。 展开更多
关键词 糖尿病 慢性脑低灌注 认知功能障碍 乙酰胆碱转移酶 胆碱能神经元 空间学习记忆
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