1Department of Neurosurgery, General Hospital of Chinese PLA, Beijing   100853, China

2Laboratory for Cell Biology, Institute of Geriatrics, General Hospital of Chinese PLA, Beijing   100853, China

Lei Liu☆, Studying for doctorate, Attending physician, Department of Neurosurgery, General Hospital of Chinese PLA, Beijing   100853, China Liu L, Xue YL, Pan JK, Hu YZ, Gao YH, Luo Y. Effects of bone morphogenetic protein-4 on spatial memory and cholinergic expression in the dentate gyrus after fornix-fimbria transection in rats. Neural Regen Res 2008;3(1):1-4

Abstract

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’s disease and other neurodegenerative diseases.

OBJECTIVE: BMP-4 was infused into the hippocampal dentate gyrus of fornix-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: Alzheimerdisease group (n = 7), normal control group (n = 5), BMP-4-Alzheimer disease group (n = 8), and model group (n = 7). In the Alzheimer disease group, the left hippocampal fornix-fimbria of rats was transected to mimic Alzheimer’s disease symptoms. In the BMP-4-Alzheimer disease group, 1 μL BMP-4 (10 mg/L) was perfused into the left dentate gyrus with a microinjector at 1 μL/min. In the model group, 1 μL 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 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 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  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  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  disease model rats alleviates central cholinergic system injury and concomitantly improves spatial memory.

Key Words: senile dementia; bone morphogenetic protein-4; hippocampus; dentate gyrus; cholinergic neuron; Alzheimer disease

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