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Electroacupuncture Mitigates Hippocampal Cognitive Impairments by Reducing BACE1 Deposition and Activating PKA in APP/PS1 Double Transgenic Mice

Increased amyloid-β (Aβ) plaque deposition is thought to be the main cause of Alzheimer’s disease (AD). β-Site amyloid precursor protein cleaving enzyme 1 (BACE1) is the key protein involved in Aβ peptide generation. Excessive expression of BACE1 might cause overproduction of neurotoxins in the cent...

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Published in:Journal of neural transplantation & plasticity 2019-01, Vol.2019 (2019), p.1-12
Main Authors: Xiang, Dulian, Li, Zhigang, Xu, Anping, Cao, Jin, Zhou, You, Guo, Yu, Shao, Shujun, Tang, Yinshan, Wu, Jihong
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container_issue 2019
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container_title Journal of neural transplantation & plasticity
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creator Xiang, Dulian
Li, Zhigang
Xu, Anping
Cao, Jin
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Shao, Shujun
Tang, Yinshan
Wu, Jihong
description Increased amyloid-β (Aβ) plaque deposition is thought to be the main cause of Alzheimer’s disease (AD). β-Site amyloid precursor protein cleaving enzyme 1 (BACE1) is the key protein involved in Aβ peptide generation. Excessive expression of BACE1 might cause overproduction of neurotoxins in the central nervous system. Previous studies indicated that BACE1 initially cleaves the amyloid precursor protein (APP) and may subsequently interfere with physiological functions of proteins such as PKA, which is recognized to be closely associated with long-term potentiation (LTP) level and can effectively ameliorate cognitive impairments. Therefore, revealing the underlying mechanism of BACE1 in the pathogenesis of AD might have a significant impact on the future development of therapeutic agents targeting dementia. This study examined the effects of electroacupuncture (EA) stimulation on BACE1, APP, and p-PKA protein levels in hippocampal tissue samples. Memory and learning abilities were assessed using the Morris water maze test after EA intervention. Immunofluorescence, immunohistochemistry, and western blot were employed to assess the distribution patterns and expression levels of BACE1, APP, and p-PKA, respectively. The results showed the downregulation of BACE1 and APP and the activation of PKA by EA. In summary, EA treatment might reduce BACE1 deposition in APP/PS1 transgenic mice and regulate PKA and its associated substrates, such as LTP to change memory and learning abilities.
doi_str_mv 10.1155/2019/2823679
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subjects Acupuncture
Advertising executives
Alzheimer's disease
Amyloid beta-protein
Amyloid beta-Protein Precursor - genetics
Amyloid Precursor Protein Secretases - metabolism
Animals
Antibodies
Aspartic Acid Endopeptidases - metabolism
Brain
Cognitive Dysfunction - metabolism
Cognitive Dysfunction - therapy
Cyclic AMP-Dependent Protein Kinases - metabolism
Dementia
Disease Models, Animal
Electroacupuncture
Enzymes
Genetic engineering
Hippocampus - metabolism
Immunohistochemistry
Kinases
Male
Maze Learning - physiology
Memory
Mice
Mice, Transgenic
Neurodegeneration
Older people
Peptides
Phosphorylation
Physiological aspects
Presenilin-1 - genetics
Proteins
Transgenic animals
title Electroacupuncture Mitigates Hippocampal Cognitive Impairments by Reducing BACE1 Deposition and Activating PKA in APP/PS1 Double Transgenic Mice
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