Electroacupuncture Enhances Cognition by Promoting Brain Glucose Metabolism and Inhibiting Inflammation in the APP/PS1 Mouse Model of Alzheimer's Disease: A Pilot Study

被引:27
作者
Xu, Anping [1 ]
Tang, Yinshan [2 ]
Zeng, Qingtao [3 ]
Wang, Xin [4 ]
Tian, Huiling [1 ]
Zhou, You [2 ]
Li, Zhigang [1 ]
机构
[1] Beijing Univ Chinese Med, Sch Acupuncture Moxibust & Tuina, Beijing 100029, Peoples R China
[2] Zhejiang Univ, Dept Rehabil & Tradit Chinese Med, Affiliated Hosp 2, Sch Med, Hangzhou, Zhejiang, Peoples R China
[3] Beijing Inst Graph Commun, Informat Engn Inst, Beijing, Peoples R China
[4] Capital Med Univ, Beijing Hosp Tradit Chinese Med, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; cognition; electroacupuncture; F-18-FDG PET; frontal lobe; glucose metabolism neuroinflammation; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; GOVERNOR VESSEL; FRONTAL-CORTEX; MEMORY; IMPAIRMENT; ACUPOINT; RECOMMENDATIONS; ACUPUNCTURE;
D O I
10.3233/JAD-200242
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Alzheimer's disease (AD) is a neurodegenerative disease, yet there is no effective treatment. Electroacupuncture (EA) is a complementary alternative medicine approach. In clinical and animal studies, EA promotes cognition in AD and vascular dementia. It has been previously reported that cognitive decline in AD might be closely related to reduced glucose intake in the brain. It is worth mentioning that the regions of glucose hypometabolism are usually found to be associated with neuroinflammation. Objective: This study is to explore whether the protective mechanism of EA on cognition is related to the regulation of glucose metabolism and neuroinflammation. Methods: APP/PS1 mice were randomly divided into AD group and the treatment (AD + EA) group. In the AD + EA group, EA was applied on Baihui (GV20) and Yintang (GV29) for 20 min and then pricked at Shuigou (GV26), once every alternate day for 4 weeks. Morris water maze (MWM) tests were performed to evaluate the effects of EA treatment on cognitive functions. F-18-FDG PET, immunofluorescence, and western blot were used to examine the mechanisms underlying EA effects. Results: From MWM tests, EA treatment significantly improved cognition of APP/PS1 mice. From the F-18-FDG PET, the levels of uptake rate of glucose in frontal lobe were higher than the AD group after EA. From immunofluorescence and western blot, amyloid(A beta) and neuroinflammation were reduced after EA. Conclusion: These results suggest that EA may prevent cognitive decline in AD mouse models by enhancing glucose metabolism and inhibiting inflammation-mediated A beta deposition in the frontal lobe.
引用
收藏
页码:387 / 400
页数:14
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