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Chronic Stress Alters Spatial Representation and Bursting Patterns of Place Cells in Behaving Mice

Chronic uncontrollable stress has been shown to produce various physiological alterations and impair mnemonic functions in the rodent hippocampus. Impacts on neuronal activities, however, have not been well investigated. The present study examined dorsal CA1 place cells to elucidate the computationa...

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Autores principales: Park, Mijeong, Kim, Chong-Hyun, Jo, Seonmi, Kim, Eun Joo, Rhim, Hyewhon, Lee, C. Justin, Kim, Jeansok J., Cho, Jeiwon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637823/
https://www.ncbi.nlm.nih.gov/pubmed/26548337
http://dx.doi.org/10.1038/srep16235
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author Park, Mijeong
Kim, Chong-Hyun
Jo, Seonmi
Kim, Eun Joo
Rhim, Hyewhon
Lee, C. Justin
Kim, Jeansok J.
Cho, Jeiwon
author_facet Park, Mijeong
Kim, Chong-Hyun
Jo, Seonmi
Kim, Eun Joo
Rhim, Hyewhon
Lee, C. Justin
Kim, Jeansok J.
Cho, Jeiwon
author_sort Park, Mijeong
collection PubMed
description Chronic uncontrollable stress has been shown to produce various physiological alterations and impair mnemonic functions in the rodent hippocampus. Impacts on neuronal activities, however, have not been well investigated. The present study examined dorsal CA1 place cells to elucidate the computational changes associated with chronic stress effects on cognitive behaviors. After administering chronic restraint stress (CRS; 6 hours/day for ≥21 consecutive days) to adult male mice, several hippocampal characteristics were examined; i.e., spatial learning, in vitro synaptic plasticity, in vivo place cell recording, and western blot analysis to determine protein levels related to learning and memory. Behaviorally, CRS significantly impeded spatial learning but enhanced non-spatial cue learning on the Morris water maze. Physiologically, CRS reduced long-term potentiation (LTP) of Schaffer collateral/commisural-CA1 pathway, phospho-αCaMKII (alpha Ca2(+)/calmodulin-dependent protein kinase II) level in the hippocampus, and stability of spatial representation and the mean firing rates (FRs) of place cells. Moreover, the local cue-dependency of place fields was increased, and the intra-burst interval (IntraBI) between consecutive spikes within a burst was prolonged following CRS. These results extend the previous findings of stress impairing LTP and spatial learning to CRS modifying physical properties of spiking in place cells that contribute to changes in navigation and synaptic plasticity.
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spelling pubmed-46378232015-11-30 Chronic Stress Alters Spatial Representation and Bursting Patterns of Place Cells in Behaving Mice Park, Mijeong Kim, Chong-Hyun Jo, Seonmi Kim, Eun Joo Rhim, Hyewhon Lee, C. Justin Kim, Jeansok J. Cho, Jeiwon Sci Rep Article Chronic uncontrollable stress has been shown to produce various physiological alterations and impair mnemonic functions in the rodent hippocampus. Impacts on neuronal activities, however, have not been well investigated. The present study examined dorsal CA1 place cells to elucidate the computational changes associated with chronic stress effects on cognitive behaviors. After administering chronic restraint stress (CRS; 6 hours/day for ≥21 consecutive days) to adult male mice, several hippocampal characteristics were examined; i.e., spatial learning, in vitro synaptic plasticity, in vivo place cell recording, and western blot analysis to determine protein levels related to learning and memory. Behaviorally, CRS significantly impeded spatial learning but enhanced non-spatial cue learning on the Morris water maze. Physiologically, CRS reduced long-term potentiation (LTP) of Schaffer collateral/commisural-CA1 pathway, phospho-αCaMKII (alpha Ca2(+)/calmodulin-dependent protein kinase II) level in the hippocampus, and stability of spatial representation and the mean firing rates (FRs) of place cells. Moreover, the local cue-dependency of place fields was increased, and the intra-burst interval (IntraBI) between consecutive spikes within a burst was prolonged following CRS. These results extend the previous findings of stress impairing LTP and spatial learning to CRS modifying physical properties of spiking in place cells that contribute to changes in navigation and synaptic plasticity. Nature Publishing Group 2015-11-09 /pmc/articles/PMC4637823/ /pubmed/26548337 http://dx.doi.org/10.1038/srep16235 Text en Copyright © 2015, Macmillan Publishers Limited 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 Article
Park, Mijeong
Kim, Chong-Hyun
Jo, Seonmi
Kim, Eun Joo
Rhim, Hyewhon
Lee, C. Justin
Kim, Jeansok J.
Cho, Jeiwon
Chronic Stress Alters Spatial Representation and Bursting Patterns of Place Cells in Behaving Mice
title Chronic Stress Alters Spatial Representation and Bursting Patterns of Place Cells in Behaving Mice
title_full Chronic Stress Alters Spatial Representation and Bursting Patterns of Place Cells in Behaving Mice
title_fullStr Chronic Stress Alters Spatial Representation and Bursting Patterns of Place Cells in Behaving Mice
title_full_unstemmed Chronic Stress Alters Spatial Representation and Bursting Patterns of Place Cells in Behaving Mice
title_short Chronic Stress Alters Spatial Representation and Bursting Patterns of Place Cells in Behaving Mice
title_sort chronic stress alters spatial representation and bursting patterns of place cells in behaving mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4637823/
https://www.ncbi.nlm.nih.gov/pubmed/26548337
http://dx.doi.org/10.1038/srep16235
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