Cargando…
Anodal Transcranial Direct Current Stimulation Can Improve Spatial Learning and Memory and Attenuate Aβ(42) Burden at the Early Stage of Alzheimer’s Disease in APP/PS1 Transgenic Mice
Alzheimer’s disease (AD) is an irreversible progressive neurodegenerative disease. Intervention in the early stage of AD is a new path for AD treatment that is being explored. The behavioral and pathological effects of anodal transcranial direct current stimulation (AtDCS) at the early stage of AD i...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239315/ https://www.ncbi.nlm.nih.gov/pubmed/32595486 http://dx.doi.org/10.3389/fnagi.2020.00134 |
_version_ | 1783536670601117696 |
---|---|
author | Luo, Yinpei Yang, Wenjuan Li, Nian Yang, Xiufang Zhu, Binglian Wang, Cong Hou, Wensheng Wang, Xing Wen, Huizhong Tian, Xuelong |
author_facet | Luo, Yinpei Yang, Wenjuan Li, Nian Yang, Xiufang Zhu, Binglian Wang, Cong Hou, Wensheng Wang, Xing Wen, Huizhong Tian, Xuelong |
author_sort | Luo, Yinpei |
collection | PubMed |
description | Alzheimer’s disease (AD) is an irreversible progressive neurodegenerative disease. Intervention in the early stage of AD is a new path for AD treatment that is being explored. The behavioral and pathological effects of anodal transcranial direct current stimulation (AtDCS) at the early stage of AD in the mouse model, amyloid precursor protein (APP)/presenilin-1 (PS1) transgenic mice, were investigated based on our previous studies. Thirty-three 6-month-old male APP/PS1 mice were randomly divided into the model group (AD group), model + sham stimulation group (ADST group) and stimulation group (ADT group). Eleven 6-month-old male C57 wild-type mice were randomly selected as a control group (CTL group). The ADT group received 10 AtDCS sessions. The Morris water maze (MWM) task and novel object recognition (NOR) task were used to test mouse memory. Nissl staining, Western blot (WB), immunohistochemistry and immunofluorescence staining of β-amyloid (Aβ(42)), glial fibrillary acidic protein (GFAP) and NF200 were conducted for pathological analysis. The ADT group and the CTL group had a shorter escape latency and more platform-region crossings than the AD group and ADST group in the MWM. There was no significant difference in the discrimination index among the groups in the NOR task. Pathological analysis showed visible differences between the AD group and ADT group. This study revealed that early-stage APP/PS1 transgenic mice did not show recognition memory impairment. AtDCS effectively improved spatial learning and memory in the early-stage APP/PS1 transgenic mouse model of AD, alleviating Aβ burden and having a protective effect on neurons. AtDCS could improve AD-related symptoms by activating many glial cells to promote the degradation and clearance of Aβ or directly affecting production and degradation of Aβ to reduce glial activation. AtDCS is an effective means of early intervention in the early stage of AD. |
format | Online Article Text |
id | pubmed-7239315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72393152020-06-26 Anodal Transcranial Direct Current Stimulation Can Improve Spatial Learning and Memory and Attenuate Aβ(42) Burden at the Early Stage of Alzheimer’s Disease in APP/PS1 Transgenic Mice Luo, Yinpei Yang, Wenjuan Li, Nian Yang, Xiufang Zhu, Binglian Wang, Cong Hou, Wensheng Wang, Xing Wen, Huizhong Tian, Xuelong Front Aging Neurosci Neuroscience Alzheimer’s disease (AD) is an irreversible progressive neurodegenerative disease. Intervention in the early stage of AD is a new path for AD treatment that is being explored. The behavioral and pathological effects of anodal transcranial direct current stimulation (AtDCS) at the early stage of AD in the mouse model, amyloid precursor protein (APP)/presenilin-1 (PS1) transgenic mice, were investigated based on our previous studies. Thirty-three 6-month-old male APP/PS1 mice were randomly divided into the model group (AD group), model + sham stimulation group (ADST group) and stimulation group (ADT group). Eleven 6-month-old male C57 wild-type mice were randomly selected as a control group (CTL group). The ADT group received 10 AtDCS sessions. The Morris water maze (MWM) task and novel object recognition (NOR) task were used to test mouse memory. Nissl staining, Western blot (WB), immunohistochemistry and immunofluorescence staining of β-amyloid (Aβ(42)), glial fibrillary acidic protein (GFAP) and NF200 were conducted for pathological analysis. The ADT group and the CTL group had a shorter escape latency and more platform-region crossings than the AD group and ADST group in the MWM. There was no significant difference in the discrimination index among the groups in the NOR task. Pathological analysis showed visible differences between the AD group and ADT group. This study revealed that early-stage APP/PS1 transgenic mice did not show recognition memory impairment. AtDCS effectively improved spatial learning and memory in the early-stage APP/PS1 transgenic mouse model of AD, alleviating Aβ burden and having a protective effect on neurons. AtDCS could improve AD-related symptoms by activating many glial cells to promote the degradation and clearance of Aβ or directly affecting production and degradation of Aβ to reduce glial activation. AtDCS is an effective means of early intervention in the early stage of AD. Frontiers Media S.A. 2020-05-13 /pmc/articles/PMC7239315/ /pubmed/32595486 http://dx.doi.org/10.3389/fnagi.2020.00134 Text en Copyright © 2020 Luo, Yang, Li, Yang, Zhu, Wang, Hou, Wang, Wen and Tian. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Luo, Yinpei Yang, Wenjuan Li, Nian Yang, Xiufang Zhu, Binglian Wang, Cong Hou, Wensheng Wang, Xing Wen, Huizhong Tian, Xuelong Anodal Transcranial Direct Current Stimulation Can Improve Spatial Learning and Memory and Attenuate Aβ(42) Burden at the Early Stage of Alzheimer’s Disease in APP/PS1 Transgenic Mice |
title | Anodal Transcranial Direct Current Stimulation Can Improve Spatial Learning and Memory and Attenuate Aβ(42) Burden at the Early Stage of Alzheimer’s Disease in APP/PS1 Transgenic Mice |
title_full | Anodal Transcranial Direct Current Stimulation Can Improve Spatial Learning and Memory and Attenuate Aβ(42) Burden at the Early Stage of Alzheimer’s Disease in APP/PS1 Transgenic Mice |
title_fullStr | Anodal Transcranial Direct Current Stimulation Can Improve Spatial Learning and Memory and Attenuate Aβ(42) Burden at the Early Stage of Alzheimer’s Disease in APP/PS1 Transgenic Mice |
title_full_unstemmed | Anodal Transcranial Direct Current Stimulation Can Improve Spatial Learning and Memory and Attenuate Aβ(42) Burden at the Early Stage of Alzheimer’s Disease in APP/PS1 Transgenic Mice |
title_short | Anodal Transcranial Direct Current Stimulation Can Improve Spatial Learning and Memory and Attenuate Aβ(42) Burden at the Early Stage of Alzheimer’s Disease in APP/PS1 Transgenic Mice |
title_sort | anodal transcranial direct current stimulation can improve spatial learning and memory and attenuate aβ(42) burden at the early stage of alzheimer’s disease in app/ps1 transgenic mice |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239315/ https://www.ncbi.nlm.nih.gov/pubmed/32595486 http://dx.doi.org/10.3389/fnagi.2020.00134 |
work_keys_str_mv | AT luoyinpei anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT yangwenjuan anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT linian anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT yangxiufang anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT zhubinglian anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT wangcong anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT houwensheng anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT wangxing anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT wenhuizhong anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice AT tianxuelong anodaltranscranialdirectcurrentstimulationcanimprovespatiallearningandmemoryandattenuateab42burdenattheearlystageofalzheimersdiseaseinappps1transgenicmice |