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Hippocampal CA1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex
The hippocampus is an essential brain area for learning and memory. However, the network mechanisms underlying memory storage, consolidation and retrieval remain incompletely understood. Place cell sequences during theta oscillations are thought to be replayed during non-theta states to support cons...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430812/ https://www.ncbi.nlm.nih.gov/pubmed/30902981 http://dx.doi.org/10.1038/s41467-019-09280-0 |
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author | Chenani, Alireza Sabariego, Marta Schlesiger, Magdalene I. Leutgeb, Jill K. Leutgeb, Stefan Leibold, Christian |
author_facet | Chenani, Alireza Sabariego, Marta Schlesiger, Magdalene I. Leutgeb, Jill K. Leutgeb, Stefan Leibold, Christian |
author_sort | Chenani, Alireza |
collection | PubMed |
description | The hippocampus is an essential brain area for learning and memory. However, the network mechanisms underlying memory storage, consolidation and retrieval remain incompletely understood. Place cell sequences during theta oscillations are thought to be replayed during non-theta states to support consolidation and route planning. In animals with medial entorhinal cortex (MEC) lesions, the temporal organization of theta-related hippocampal activity is disrupted, which allows us to test whether replay is also compromised. Two different analyses—comparison of co-activation patterns between running and rest epochs and analysis of the recurrence of place cell sequences—reveal that the enhancement of replay by behavior is reduced in MEC-lesioned versus control rats. In contrast, the degree of intrinsic network structure prior and subsequent to behavior remains unaffected by MEC lesions. The MEC-dependent temporal coordination during theta states therefore appears to facilitate behavior-related plasticity, but does not disrupt pre-existing functional connectivity. |
format | Online Article Text |
id | pubmed-6430812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64308122019-03-25 Hippocampal CA1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex Chenani, Alireza Sabariego, Marta Schlesiger, Magdalene I. Leutgeb, Jill K. Leutgeb, Stefan Leibold, Christian Nat Commun Article The hippocampus is an essential brain area for learning and memory. However, the network mechanisms underlying memory storage, consolidation and retrieval remain incompletely understood. Place cell sequences during theta oscillations are thought to be replayed during non-theta states to support consolidation and route planning. In animals with medial entorhinal cortex (MEC) lesions, the temporal organization of theta-related hippocampal activity is disrupted, which allows us to test whether replay is also compromised. Two different analyses—comparison of co-activation patterns between running and rest epochs and analysis of the recurrence of place cell sequences—reveal that the enhancement of replay by behavior is reduced in MEC-lesioned versus control rats. In contrast, the degree of intrinsic network structure prior and subsequent to behavior remains unaffected by MEC lesions. The MEC-dependent temporal coordination during theta states therefore appears to facilitate behavior-related plasticity, but does not disrupt pre-existing functional connectivity. Nature Publishing Group UK 2019-03-22 /pmc/articles/PMC6430812/ /pubmed/30902981 http://dx.doi.org/10.1038/s41467-019-09280-0 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Chenani, Alireza Sabariego, Marta Schlesiger, Magdalene I. Leutgeb, Jill K. Leutgeb, Stefan Leibold, Christian Hippocampal CA1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex |
title | Hippocampal CA1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex |
title_full | Hippocampal CA1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex |
title_fullStr | Hippocampal CA1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex |
title_full_unstemmed | Hippocampal CA1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex |
title_short | Hippocampal CA1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex |
title_sort | hippocampal ca1 replay becomes less prominent but more rigid without inputs from medial entorhinal cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430812/ https://www.ncbi.nlm.nih.gov/pubmed/30902981 http://dx.doi.org/10.1038/s41467-019-09280-0 |
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