Cargando…

Treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via BDNF/TrkB pathway

Stress-related memory deficit is correlated with dendritic spine loss. Physical exercise improves memory function and promotes spinogenesis. However, no studies have been performed to directly observe exercise-related effects on spine dynamics, in association with memory function. This study utilize...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, K, Zhang, L, Tan, M, Lai, C S W, Li, A, Ren, C, So, K-F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416682/
https://www.ncbi.nlm.nih.gov/pubmed/28323283
http://dx.doi.org/10.1038/tp.2017.41
_version_ 1783233797282594816
author Chen, K
Zhang, L
Tan, M
Lai, C S W
Li, A
Ren, C
So, K-F
author_facet Chen, K
Zhang, L
Tan, M
Lai, C S W
Li, A
Ren, C
So, K-F
author_sort Chen, K
collection PubMed
description Stress-related memory deficit is correlated with dendritic spine loss. Physical exercise improves memory function and promotes spinogenesis. However, no studies have been performed to directly observe exercise-related effects on spine dynamics, in association with memory function. This study utilized transcranial two-photon in vivo microscopy to investigate dendritic spine formation and elimination in barrel cortex of mice under physical constrain or naive conditions, followed by memory performance in a whisker-dependent novel texture discrimination task. We found that stressed mice had elevated spine elimination rate in mouse barrel cortex plus deficits in memory retrieval, both of which can be rescued by chronic exercise on treadmill. Exercise also elevated brain-derived neurotrophic factor (BDNF) expression in barrel cortex. The above-mentioned rescuing effects for both spinognesis and memory function were abolished after inhibiting BDNF/tyrosine kinase B (TrkB) pathway. In summary, this study demonstrated the improvement of stress-associated memory function by exercise via facilitating spine retention in a BDNF/TrkB-dependent manner.
format Online
Article
Text
id pubmed-5416682
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-54166822017-05-12 Treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via BDNF/TrkB pathway Chen, K Zhang, L Tan, M Lai, C S W Li, A Ren, C So, K-F Transl Psychiatry Original Article Stress-related memory deficit is correlated with dendritic spine loss. Physical exercise improves memory function and promotes spinogenesis. However, no studies have been performed to directly observe exercise-related effects on spine dynamics, in association with memory function. This study utilized transcranial two-photon in vivo microscopy to investigate dendritic spine formation and elimination in barrel cortex of mice under physical constrain or naive conditions, followed by memory performance in a whisker-dependent novel texture discrimination task. We found that stressed mice had elevated spine elimination rate in mouse barrel cortex plus deficits in memory retrieval, both of which can be rescued by chronic exercise on treadmill. Exercise also elevated brain-derived neurotrophic factor (BDNF) expression in barrel cortex. The above-mentioned rescuing effects for both spinognesis and memory function were abolished after inhibiting BDNF/tyrosine kinase B (TrkB) pathway. In summary, this study demonstrated the improvement of stress-associated memory function by exercise via facilitating spine retention in a BDNF/TrkB-dependent manner. Nature Publishing Group 2017-03 2017-03-21 /pmc/articles/PMC5416682/ /pubmed/28323283 http://dx.doi.org/10.1038/tp.2017.41 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Chen, K
Zhang, L
Tan, M
Lai, C S W
Li, A
Ren, C
So, K-F
Treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via BDNF/TrkB pathway
title Treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via BDNF/TrkB pathway
title_full Treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via BDNF/TrkB pathway
title_fullStr Treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via BDNF/TrkB pathway
title_full_unstemmed Treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via BDNF/TrkB pathway
title_short Treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via BDNF/TrkB pathway
title_sort treadmill exercise suppressed stress-induced dendritic spine elimination in mouse barrel cortex and improved working memory via bdnf/trkb pathway
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5416682/
https://www.ncbi.nlm.nih.gov/pubmed/28323283
http://dx.doi.org/10.1038/tp.2017.41
work_keys_str_mv AT chenk treadmillexercisesuppressedstressinduceddendriticspineeliminationinmousebarrelcortexandimprovedworkingmemoryviabdnftrkbpathway
AT zhangl treadmillexercisesuppressedstressinduceddendriticspineeliminationinmousebarrelcortexandimprovedworkingmemoryviabdnftrkbpathway
AT tanm treadmillexercisesuppressedstressinduceddendriticspineeliminationinmousebarrelcortexandimprovedworkingmemoryviabdnftrkbpathway
AT laicsw treadmillexercisesuppressedstressinduceddendriticspineeliminationinmousebarrelcortexandimprovedworkingmemoryviabdnftrkbpathway
AT lia treadmillexercisesuppressedstressinduceddendriticspineeliminationinmousebarrelcortexandimprovedworkingmemoryviabdnftrkbpathway
AT renc treadmillexercisesuppressedstressinduceddendriticspineeliminationinmousebarrelcortexandimprovedworkingmemoryviabdnftrkbpathway
AT sokf treadmillexercisesuppressedstressinduceddendriticspineeliminationinmousebarrelcortexandimprovedworkingmemoryviabdnftrkbpathway