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Electroacupuncture Attenuates Learning and Memory Impairment via PI3K/Akt Pathway in an Amyloid β(25-35)-Induced Alzheimer's Disease Mouse Model

The main characteristic of Alzheimer's disease (AD) is the progressive decline of learning and memory ability. Electroacupuncture (EA) may improve AD-related learning and memory ability. However, the underlying molecular mechanism of action remains unclear. The objective of the present study wa...

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Autores principales: Shao, Si-Mai, Park, Kyung Hye, Yuan, Ye, Zhang, Zijuan, You, Yanwen, Zhang, Zhenqiang, Hao, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033336/
https://www.ncbi.nlm.nih.gov/pubmed/35463064
http://dx.doi.org/10.1155/2022/3849441
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author Shao, Si-Mai
Park, Kyung Hye
Yuan, Ye
Zhang, Zijuan
You, Yanwen
Zhang, Zhenqiang
Hao, Li
author_facet Shao, Si-Mai
Park, Kyung Hye
Yuan, Ye
Zhang, Zijuan
You, Yanwen
Zhang, Zhenqiang
Hao, Li
author_sort Shao, Si-Mai
collection PubMed
description The main characteristic of Alzheimer's disease (AD) is the progressive decline of learning and memory ability. Electroacupuncture (EA) may improve AD-related learning and memory ability. However, the underlying molecular mechanism of action remains unclear. The objective of the present study was to assess the effects and the molecular mechanism of EA on learning and memory in an amyloid β(25-35) (Aβ(25-35)) induced AD mouse model. The AD model was established by intracerebroventricular (ICV) administration of Aβ(25-35) oligomers. AD mice were electroacupunctured with wisdom three-needle combined with Baihui (GV20) five times per week for three consecutive weeks. The Morris water maze (MWM) and Y maze tests were applied to evaluate spatial learning and memory ability. A transmission electron microscope (TEM) was used to measure mitochondria and autophagy of hippocampal neurons, and western blot was applied to observe molecular changes in the mice hippocampus. The results suggested that EA treatment significantly alleviated learning and memory impairment related to AD, reduced mitochondria damage, improved autophagy, increased mitochondrial protein 2 (Mfn2), Beclin 1, and LC3B, and decreased the expressions of fission protein 1 (Fis1) level. Furthermore, EA further upregulated the protein expression of phosphatidylinositol 3-kinase (PI3K) and the ratio of p-Akt/Akt in the hippocampus of AD mice. This study demonstrates that EA treatment attenuates cognitive deficits, modulates mitochondrial fusion and fission, and enhances autophagy via the PI3K/Akt pathway in a mouse AD model.
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spelling pubmed-90333362022-04-23 Electroacupuncture Attenuates Learning and Memory Impairment via PI3K/Akt Pathway in an Amyloid β(25-35)-Induced Alzheimer's Disease Mouse Model Shao, Si-Mai Park, Kyung Hye Yuan, Ye Zhang, Zijuan You, Yanwen Zhang, Zhenqiang Hao, Li Evid Based Complement Alternat Med Research Article The main characteristic of Alzheimer's disease (AD) is the progressive decline of learning and memory ability. Electroacupuncture (EA) may improve AD-related learning and memory ability. However, the underlying molecular mechanism of action remains unclear. The objective of the present study was to assess the effects and the molecular mechanism of EA on learning and memory in an amyloid β(25-35) (Aβ(25-35)) induced AD mouse model. The AD model was established by intracerebroventricular (ICV) administration of Aβ(25-35) oligomers. AD mice were electroacupunctured with wisdom three-needle combined with Baihui (GV20) five times per week for three consecutive weeks. The Morris water maze (MWM) and Y maze tests were applied to evaluate spatial learning and memory ability. A transmission electron microscope (TEM) was used to measure mitochondria and autophagy of hippocampal neurons, and western blot was applied to observe molecular changes in the mice hippocampus. The results suggested that EA treatment significantly alleviated learning and memory impairment related to AD, reduced mitochondria damage, improved autophagy, increased mitochondrial protein 2 (Mfn2), Beclin 1, and LC3B, and decreased the expressions of fission protein 1 (Fis1) level. Furthermore, EA further upregulated the protein expression of phosphatidylinositol 3-kinase (PI3K) and the ratio of p-Akt/Akt in the hippocampus of AD mice. This study demonstrates that EA treatment attenuates cognitive deficits, modulates mitochondrial fusion and fission, and enhances autophagy via the PI3K/Akt pathway in a mouse AD model. Hindawi 2022-04-15 /pmc/articles/PMC9033336/ /pubmed/35463064 http://dx.doi.org/10.1155/2022/3849441 Text en Copyright © 2022 Si-Mai Shao et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shao, Si-Mai
Park, Kyung Hye
Yuan, Ye
Zhang, Zijuan
You, Yanwen
Zhang, Zhenqiang
Hao, Li
Electroacupuncture Attenuates Learning and Memory Impairment via PI3K/Akt Pathway in an Amyloid β(25-35)-Induced Alzheimer's Disease Mouse Model
title Electroacupuncture Attenuates Learning and Memory Impairment via PI3K/Akt Pathway in an Amyloid β(25-35)-Induced Alzheimer's Disease Mouse Model
title_full Electroacupuncture Attenuates Learning and Memory Impairment via PI3K/Akt Pathway in an Amyloid β(25-35)-Induced Alzheimer's Disease Mouse Model
title_fullStr Electroacupuncture Attenuates Learning and Memory Impairment via PI3K/Akt Pathway in an Amyloid β(25-35)-Induced Alzheimer's Disease Mouse Model
title_full_unstemmed Electroacupuncture Attenuates Learning and Memory Impairment via PI3K/Akt Pathway in an Amyloid β(25-35)-Induced Alzheimer's Disease Mouse Model
title_short Electroacupuncture Attenuates Learning and Memory Impairment via PI3K/Akt Pathway in an Amyloid β(25-35)-Induced Alzheimer's Disease Mouse Model
title_sort electroacupuncture attenuates learning and memory impairment via pi3k/akt pathway in an amyloid β(25-35)-induced alzheimer's disease mouse model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033336/
https://www.ncbi.nlm.nih.gov/pubmed/35463064
http://dx.doi.org/10.1155/2022/3849441
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