Deep Brain Magnetic Stimulation Promotes Neurogenesis and Restores Cholinergic Activity in a Transgenic Mouse Model of Alzheimer's Disease

被引:34
作者
Zhen, Junli [1 ,2 ,3 ]
Qian, Yanjing [1 ,2 ]
Fu, Jian [3 ]
Su, Ruijun [1 ,2 ]
An, Haiting [1 ,2 ]
Wang, Wei [1 ,2 ]
Zheng, Yan [1 ,2 ]
Wang, Xiaomin [1 ,2 ]
机构
[1] Capital Med Univ, Dept Neurobiol, Key Lab Neurodegenerat Disorders, Minist Educ, Beijing, Peoples R China
[2] Beijing Inst Brain Disorders, Beijing, Peoples R China
[3] Hebei Med Univ, Hosp 2, Shijiazhuang, Peoples R China
来源
FRONTIERS IN NEURAL CIRCUITS | 2017年 / 11卷
关键词
Alzheimer's disease; hippocampus; cognition; neurogenesis; cholinergic activity; ADULT HIPPOCAMPAL NEUROGENESIS; CELLS; BETA; ENHANCEMENT; SURVIVAL; MICE; BRDU;
D O I
10.3389/fncir.2017.00048
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is characterized by progressive decline of memory and cognitive functions. Deep magnetic stimulation (DMS), a noninvasive and nonpharmacological brain stimulation, has been reported to alleviate stress-related cognitive impairment in neuropsychiatric disorders. Our previous study also discovered the preventive effect of DMS on cognitive decline in an AD mouse model. However, the underlying mechanism must be explored further. In this study, we investigated the effect of DMS on spatial learning and memory functions, neurogenesis in the dentate gyrus (DG), as well as expression and activity of the cholinergic system in a transgenic mouse model of AD (5XFAD). Administration of DMS effectively improved performance in spatial learning and memory of 5XFAD mice. Furthermore, neurogenesis in the hippocampal DG of DMS-treated 5XFAD mice was clearly enhanced. In addition, DMS significantly raised the level of acetylcholine and prevented the increase in acetylcholinesterase activity as well as the decrease in acetyltransferase activity in the hippocampus of 5XFAD mice. These findings indicate that DMS may be a promising noninvasive tool for treatment and prevention of AD cognitive impairment by promoting neurogenesis and enhancing cholinergic system function.
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页数:8
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