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Short-Range Temporal Interactions in Sleep; Hippocampal Spike Avalanches Support a Large Milieu of Sequential Activity Including Replay

Hippocampal neural systems consolidate multiple complex behaviors into memory. However, the temporal structure of neural firing supporting complex memory consolidation is unknown. Replay of hippocampal place cells during sleep supports the view that a simple repetitive behavior modifies sleep firing...

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Detalles Bibliográficos
Autores principales: Mahoney, J. Matthew, Titiz, Ali S., Hernan, Amanda E., Scott, Rod C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750866/
https://www.ncbi.nlm.nih.gov/pubmed/26866597
http://dx.doi.org/10.1371/journal.pone.0147708
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author Mahoney, J. Matthew
Titiz, Ali S.
Hernan, Amanda E.
Scott, Rod C.
author_facet Mahoney, J. Matthew
Titiz, Ali S.
Hernan, Amanda E.
Scott, Rod C.
author_sort Mahoney, J. Matthew
collection PubMed
description Hippocampal neural systems consolidate multiple complex behaviors into memory. However, the temporal structure of neural firing supporting complex memory consolidation is unknown. Replay of hippocampal place cells during sleep supports the view that a simple repetitive behavior modifies sleep firing dynamics, but does not explain how multiple episodes could be integrated into associative networks for recollection during future cognition. Here we decode sequential firing structure within spike avalanches of all pyramidal cells recorded in sleeping rats after running in a circular track. We find that short sequences that combine into multiple long sequences capture the majority of the sequential structure during sleep, including replay of hippocampal place cells. The ensemble, however, is not optimized for maximally producing the behavior-enriched episode. Thus behavioral programming of sequential correlations occurs at the level of short-range interactions, not whole behavioral sequences and these short sequences are assembled into a large and complex milieu that could support complex memory consolidation.
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spelling pubmed-47508662016-02-26 Short-Range Temporal Interactions in Sleep; Hippocampal Spike Avalanches Support a Large Milieu of Sequential Activity Including Replay Mahoney, J. Matthew Titiz, Ali S. Hernan, Amanda E. Scott, Rod C. PLoS One Research Article Hippocampal neural systems consolidate multiple complex behaviors into memory. However, the temporal structure of neural firing supporting complex memory consolidation is unknown. Replay of hippocampal place cells during sleep supports the view that a simple repetitive behavior modifies sleep firing dynamics, but does not explain how multiple episodes could be integrated into associative networks for recollection during future cognition. Here we decode sequential firing structure within spike avalanches of all pyramidal cells recorded in sleeping rats after running in a circular track. We find that short sequences that combine into multiple long sequences capture the majority of the sequential structure during sleep, including replay of hippocampal place cells. The ensemble, however, is not optimized for maximally producing the behavior-enriched episode. Thus behavioral programming of sequential correlations occurs at the level of short-range interactions, not whole behavioral sequences and these short sequences are assembled into a large and complex milieu that could support complex memory consolidation. Public Library of Science 2016-02-11 /pmc/articles/PMC4750866/ /pubmed/26866597 http://dx.doi.org/10.1371/journal.pone.0147708 Text en © 2016 Mahoney et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Mahoney, J. Matthew
Titiz, Ali S.
Hernan, Amanda E.
Scott, Rod C.
Short-Range Temporal Interactions in Sleep; Hippocampal Spike Avalanches Support a Large Milieu of Sequential Activity Including Replay
title Short-Range Temporal Interactions in Sleep; Hippocampal Spike Avalanches Support a Large Milieu of Sequential Activity Including Replay
title_full Short-Range Temporal Interactions in Sleep; Hippocampal Spike Avalanches Support a Large Milieu of Sequential Activity Including Replay
title_fullStr Short-Range Temporal Interactions in Sleep; Hippocampal Spike Avalanches Support a Large Milieu of Sequential Activity Including Replay
title_full_unstemmed Short-Range Temporal Interactions in Sleep; Hippocampal Spike Avalanches Support a Large Milieu of Sequential Activity Including Replay
title_short Short-Range Temporal Interactions in Sleep; Hippocampal Spike Avalanches Support a Large Milieu of Sequential Activity Including Replay
title_sort short-range temporal interactions in sleep; hippocampal spike avalanches support a large milieu of sequential activity including replay
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750866/
https://www.ncbi.nlm.nih.gov/pubmed/26866597
http://dx.doi.org/10.1371/journal.pone.0147708
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