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Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events

The hippocampus is critical to the temporal organization of our experiences. Although this fundamental capacity is conserved across modalities and species, its underlying neuronal mechanisms remain unclear. Here we recorded hippocampal activity as rats remembered an extended sequence of nonspatial e...

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Autores principales: Shahbaba, Babak, Li, Lingge, Agostinelli, Forest, Saraf, Mansi, Cooper, Keiland W., Haghverdian, Derenik, Elias, Gabriel A., Baldi, Pierre, Fortin, Norbert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825855/
https://www.ncbi.nlm.nih.gov/pubmed/35136052
http://dx.doi.org/10.1038/s41467-022-28057-6
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author Shahbaba, Babak
Li, Lingge
Agostinelli, Forest
Saraf, Mansi
Cooper, Keiland W.
Haghverdian, Derenik
Elias, Gabriel A.
Baldi, Pierre
Fortin, Norbert J.
author_facet Shahbaba, Babak
Li, Lingge
Agostinelli, Forest
Saraf, Mansi
Cooper, Keiland W.
Haghverdian, Derenik
Elias, Gabriel A.
Baldi, Pierre
Fortin, Norbert J.
author_sort Shahbaba, Babak
collection PubMed
description The hippocampus is critical to the temporal organization of our experiences. Although this fundamental capacity is conserved across modalities and species, its underlying neuronal mechanisms remain unclear. Here we recorded hippocampal activity as rats remembered an extended sequence of nonspatial events unfolding over several seconds, as in daily life episodes in humans. We then developed statistical machine learning methods to analyze the ensemble activity and discovered forms of sequential organization and coding important for order memory judgments. Specifically, we found that hippocampal ensembles provide significant temporal coding throughout nonspatial event sequences, differentiate distinct types of task-critical information sequentially within events, and exhibit theta-associated reactivation of the sequential relationships among events. We also demonstrate that nonspatial event representations are sequentially organized within individual theta cycles and precess across successive cycles. These findings suggest a fundamental function of the hippocampal network is to encode, preserve, and predict the sequential order of experiences.
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spelling pubmed-88258552022-02-18 Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events Shahbaba, Babak Li, Lingge Agostinelli, Forest Saraf, Mansi Cooper, Keiland W. Haghverdian, Derenik Elias, Gabriel A. Baldi, Pierre Fortin, Norbert J. Nat Commun Article The hippocampus is critical to the temporal organization of our experiences. Although this fundamental capacity is conserved across modalities and species, its underlying neuronal mechanisms remain unclear. Here we recorded hippocampal activity as rats remembered an extended sequence of nonspatial events unfolding over several seconds, as in daily life episodes in humans. We then developed statistical machine learning methods to analyze the ensemble activity and discovered forms of sequential organization and coding important for order memory judgments. Specifically, we found that hippocampal ensembles provide significant temporal coding throughout nonspatial event sequences, differentiate distinct types of task-critical information sequentially within events, and exhibit theta-associated reactivation of the sequential relationships among events. We also demonstrate that nonspatial event representations are sequentially organized within individual theta cycles and precess across successive cycles. These findings suggest a fundamental function of the hippocampal network is to encode, preserve, and predict the sequential order of experiences. Nature Publishing Group UK 2022-02-08 /pmc/articles/PMC8825855/ /pubmed/35136052 http://dx.doi.org/10.1038/s41467-022-28057-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shahbaba, Babak
Li, Lingge
Agostinelli, Forest
Saraf, Mansi
Cooper, Keiland W.
Haghverdian, Derenik
Elias, Gabriel A.
Baldi, Pierre
Fortin, Norbert J.
Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events
title Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events
title_full Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events
title_fullStr Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events
title_full_unstemmed Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events
title_short Hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events
title_sort hippocampal ensembles represent sequential relationships among an extended sequence of nonspatial events
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825855/
https://www.ncbi.nlm.nih.gov/pubmed/35136052
http://dx.doi.org/10.1038/s41467-022-28057-6
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