Cargando…
Electroacupuncture Ameliorates Learning and Memory and Improves Synaptic Plasticity via Activation of the PKA/CREB Signaling Pathway in Cerebral Hypoperfusion
Electroacupuncture (EA) has shown protective effects on cognitive decline. However, the underlying molecular mechanisms are ill-understood. The present study was undertaken to determine whether the cognitive function was ameliorated in cerebral hypoperfusion rats following EA and to investigate the...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088321/ https://www.ncbi.nlm.nih.gov/pubmed/27829866 http://dx.doi.org/10.1155/2016/7893710 |
_version_ | 1782464070724616192 |
---|---|
author | Zheng, Cai-Xia Lu, Min Guo, Ya-Bi Zhang, Feng-Xia Liu, Hua Guo, Feng Huang, Xiao-Lin Han, Xiao-Hua |
author_facet | Zheng, Cai-Xia Lu, Min Guo, Ya-Bi Zhang, Feng-Xia Liu, Hua Guo, Feng Huang, Xiao-Lin Han, Xiao-Hua |
author_sort | Zheng, Cai-Xia |
collection | PubMed |
description | Electroacupuncture (EA) has shown protective effects on cognitive decline. However, the underlying molecular mechanisms are ill-understood. The present study was undertaken to determine whether the cognitive function was ameliorated in cerebral hypoperfusion rats following EA and to investigate the role of PKA/CREB pathway. We used a rat 2-vessel occlusion (2VO) model and delivered EA at Baihui (GV20) and Dazhui (GV14) acupoints. Morris water maze (MWM) task, electrophysiological recording, Golgi silver stain, Nissl stain, Western blot, and real-time PCR were employed. EA significantly (1) ameliorated the spatial learning and memory deficits, (2) alleviated long-term potentiation (LTP) impairment and the reduction of dendritic spine density, (3) suppressed the decline of phospho-CREB (pCREB) protein, brain-derived neurotrophic factor (BDNF) protein, and microRNA132 (miR132), and (4) reduced the increase of p250GAP protein of 2VO rats. These changes were partially blocked by a selective protein kinase A (PKA) inhibitor, N-[2-(p-bromocinnamylamino)ethyl]-5-isoquinoline-sulfonamide (H89), suggesting that the PKA/CREB pathway is potentially involved in the effects of EA. Moreover, any significant damage to the pyramidal cell layer of CA1 subregion was absent. These results demonstrated that EA could ameliorate learning and memory deficits and alleviate hippocampal synaptic plasticity impairment of cerebral hypoperfusion rats, potentially mediated by PKA/CREB signaling pathway. |
format | Online Article Text |
id | pubmed-5088321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-50883212016-11-09 Electroacupuncture Ameliorates Learning and Memory and Improves Synaptic Plasticity via Activation of the PKA/CREB Signaling Pathway in Cerebral Hypoperfusion Zheng, Cai-Xia Lu, Min Guo, Ya-Bi Zhang, Feng-Xia Liu, Hua Guo, Feng Huang, Xiao-Lin Han, Xiao-Hua Evid Based Complement Alternat Med Research Article Electroacupuncture (EA) has shown protective effects on cognitive decline. However, the underlying molecular mechanisms are ill-understood. The present study was undertaken to determine whether the cognitive function was ameliorated in cerebral hypoperfusion rats following EA and to investigate the role of PKA/CREB pathway. We used a rat 2-vessel occlusion (2VO) model and delivered EA at Baihui (GV20) and Dazhui (GV14) acupoints. Morris water maze (MWM) task, electrophysiological recording, Golgi silver stain, Nissl stain, Western blot, and real-time PCR were employed. EA significantly (1) ameliorated the spatial learning and memory deficits, (2) alleviated long-term potentiation (LTP) impairment and the reduction of dendritic spine density, (3) suppressed the decline of phospho-CREB (pCREB) protein, brain-derived neurotrophic factor (BDNF) protein, and microRNA132 (miR132), and (4) reduced the increase of p250GAP protein of 2VO rats. These changes were partially blocked by a selective protein kinase A (PKA) inhibitor, N-[2-(p-bromocinnamylamino)ethyl]-5-isoquinoline-sulfonamide (H89), suggesting that the PKA/CREB pathway is potentially involved in the effects of EA. Moreover, any significant damage to the pyramidal cell layer of CA1 subregion was absent. These results demonstrated that EA could ameliorate learning and memory deficits and alleviate hippocampal synaptic plasticity impairment of cerebral hypoperfusion rats, potentially mediated by PKA/CREB signaling pathway. Hindawi Publishing Corporation 2016 2016-10-18 /pmc/articles/PMC5088321/ /pubmed/27829866 http://dx.doi.org/10.1155/2016/7893710 Text en Copyright © 2016 Cai-Xia Zheng 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 Zheng, Cai-Xia Lu, Min Guo, Ya-Bi Zhang, Feng-Xia Liu, Hua Guo, Feng Huang, Xiao-Lin Han, Xiao-Hua Electroacupuncture Ameliorates Learning and Memory and Improves Synaptic Plasticity via Activation of the PKA/CREB Signaling Pathway in Cerebral Hypoperfusion |
title | Electroacupuncture Ameliorates Learning and Memory and Improves Synaptic Plasticity via Activation of the PKA/CREB Signaling Pathway in Cerebral Hypoperfusion |
title_full | Electroacupuncture Ameliorates Learning and Memory and Improves Synaptic Plasticity via Activation of the PKA/CREB Signaling Pathway in Cerebral Hypoperfusion |
title_fullStr | Electroacupuncture Ameliorates Learning and Memory and Improves Synaptic Plasticity via Activation of the PKA/CREB Signaling Pathway in Cerebral Hypoperfusion |
title_full_unstemmed | Electroacupuncture Ameliorates Learning and Memory and Improves Synaptic Plasticity via Activation of the PKA/CREB Signaling Pathway in Cerebral Hypoperfusion |
title_short | Electroacupuncture Ameliorates Learning and Memory and Improves Synaptic Plasticity via Activation of the PKA/CREB Signaling Pathway in Cerebral Hypoperfusion |
title_sort | electroacupuncture ameliorates learning and memory and improves synaptic plasticity via activation of the pka/creb signaling pathway in cerebral hypoperfusion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088321/ https://www.ncbi.nlm.nih.gov/pubmed/27829866 http://dx.doi.org/10.1155/2016/7893710 |
work_keys_str_mv | AT zhengcaixia electroacupunctureameliorateslearningandmemoryandimprovessynapticplasticityviaactivationofthepkacrebsignalingpathwayincerebralhypoperfusion AT lumin electroacupunctureameliorateslearningandmemoryandimprovessynapticplasticityviaactivationofthepkacrebsignalingpathwayincerebralhypoperfusion AT guoyabi electroacupunctureameliorateslearningandmemoryandimprovessynapticplasticityviaactivationofthepkacrebsignalingpathwayincerebralhypoperfusion AT zhangfengxia electroacupunctureameliorateslearningandmemoryandimprovessynapticplasticityviaactivationofthepkacrebsignalingpathwayincerebralhypoperfusion AT liuhua electroacupunctureameliorateslearningandmemoryandimprovessynapticplasticityviaactivationofthepkacrebsignalingpathwayincerebralhypoperfusion AT guofeng electroacupunctureameliorateslearningandmemoryandimprovessynapticplasticityviaactivationofthepkacrebsignalingpathwayincerebralhypoperfusion AT huangxiaolin electroacupunctureameliorateslearningandmemoryandimprovessynapticplasticityviaactivationofthepkacrebsignalingpathwayincerebralhypoperfusion AT hanxiaohua electroacupunctureameliorateslearningandmemoryandimprovessynapticplasticityviaactivationofthepkacrebsignalingpathwayincerebralhypoperfusion |