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Hippocampal awake replay in fear memory retrieval

Hippocampal place cells are key to episodic memories. How these cells participate in memory retrieval remains unclear. Here, after rats acquired a fear memory by receiving mild foot-shocks at a shock zone of a track, we analyzed place cells when the animals were placed back to the track and displaye...

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Detalles Bibliográficos
Autores principales: Wu, Chun-Ting, Haggerty, Daniel, Kemere, Caleb, Ji, Daoyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373994/
https://www.ncbi.nlm.nih.gov/pubmed/28218916
http://dx.doi.org/10.1038/nn.4507
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author Wu, Chun-Ting
Haggerty, Daniel
Kemere, Caleb
Ji, Daoyun
author_facet Wu, Chun-Ting
Haggerty, Daniel
Kemere, Caleb
Ji, Daoyun
author_sort Wu, Chun-Ting
collection PubMed
description Hippocampal place cells are key to episodic memories. How these cells participate in memory retrieval remains unclear. Here, after rats acquired a fear memory by receiving mild foot-shocks at a shock zone of a track, we analyzed place cells when the animals were placed back to the track and displayed an apparent memory retrieval behavior: avoidance of the shock zone. We found that place cells representing the shock zone were reactivated, despite the fact that the animals did not enter the shock zone. This reactivation occurred in ripple-associated awake replay of place cell sequences encoding the paths from the animal’s current positions to the shock zone, but not in place cell sequences within individual cycles of theta oscillation. The result reveals a specific place cell pattern underlying the inhibitory avoidance behavior and provides strong evidence for the involvement of awake replay in fear memory retrieval.
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spelling pubmed-53739942017-08-20 Hippocampal awake replay in fear memory retrieval Wu, Chun-Ting Haggerty, Daniel Kemere, Caleb Ji, Daoyun Nat Neurosci Article Hippocampal place cells are key to episodic memories. How these cells participate in memory retrieval remains unclear. Here, after rats acquired a fear memory by receiving mild foot-shocks at a shock zone of a track, we analyzed place cells when the animals were placed back to the track and displayed an apparent memory retrieval behavior: avoidance of the shock zone. We found that place cells representing the shock zone were reactivated, despite the fact that the animals did not enter the shock zone. This reactivation occurred in ripple-associated awake replay of place cell sequences encoding the paths from the animal’s current positions to the shock zone, but not in place cell sequences within individual cycles of theta oscillation. The result reveals a specific place cell pattern underlying the inhibitory avoidance behavior and provides strong evidence for the involvement of awake replay in fear memory retrieval. 2017-02-20 2017-04 /pmc/articles/PMC5373994/ /pubmed/28218916 http://dx.doi.org/10.1038/nn.4507 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Wu, Chun-Ting
Haggerty, Daniel
Kemere, Caleb
Ji, Daoyun
Hippocampal awake replay in fear memory retrieval
title Hippocampal awake replay in fear memory retrieval
title_full Hippocampal awake replay in fear memory retrieval
title_fullStr Hippocampal awake replay in fear memory retrieval
title_full_unstemmed Hippocampal awake replay in fear memory retrieval
title_short Hippocampal awake replay in fear memory retrieval
title_sort hippocampal awake replay in fear memory retrieval
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5373994/
https://www.ncbi.nlm.nih.gov/pubmed/28218916
http://dx.doi.org/10.1038/nn.4507
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