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Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation

Hippocampal (HPC) theta oscillation during post-training rapid eye movement (REM) sleep supports spatial learning. Theta also modulates neuronal and oscillatory activity in the retrosplenial cortex (RSC) during REM sleep. To investigate the relevance of theta-driven interaction between these two reg...

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Autores principales: de Almeida-Filho, Daniel Gomes, Koike, Bruna Del Vechio, Billwiller, Francesca, Farias, Kelly Soares, de Sales, Igor Rafael Praxedes, Luppi, Pierre-Hervé, Ribeiro, Sidarta, Queiroz, Claudio Marcos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219679/
https://www.ncbi.nlm.nih.gov/pubmed/34158548
http://dx.doi.org/10.1038/s41598-021-91659-5
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author de Almeida-Filho, Daniel Gomes
Koike, Bruna Del Vechio
Billwiller, Francesca
Farias, Kelly Soares
de Sales, Igor Rafael Praxedes
Luppi, Pierre-Hervé
Ribeiro, Sidarta
Queiroz, Claudio Marcos
author_facet de Almeida-Filho, Daniel Gomes
Koike, Bruna Del Vechio
Billwiller, Francesca
Farias, Kelly Soares
de Sales, Igor Rafael Praxedes
Luppi, Pierre-Hervé
Ribeiro, Sidarta
Queiroz, Claudio Marcos
author_sort de Almeida-Filho, Daniel Gomes
collection PubMed
description Hippocampal (HPC) theta oscillation during post-training rapid eye movement (REM) sleep supports spatial learning. Theta also modulates neuronal and oscillatory activity in the retrosplenial cortex (RSC) during REM sleep. To investigate the relevance of theta-driven interaction between these two regions to memory consolidation, we computed the Granger causality within theta range on electrophysiological data recorded in freely behaving rats during REM sleep, both before and after contextual fear conditioning. We found a training-induced modulation of causality between HPC and RSC that was correlated with memory retrieval 24 h later. Retrieval was proportional to the change in the relative influence RSC exerted upon HPC theta oscillation. Importantly, causality peaked during theta acceleration, in synchrony with phasic REM sleep. Altogether, these results support a role for phasic REM sleep in hippocampo-cortical memory consolidation and suggest that causality modulation between RSC and HPC during REM sleep plays a functional role in that phenomenon.
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spelling pubmed-82196792021-06-24 Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation de Almeida-Filho, Daniel Gomes Koike, Bruna Del Vechio Billwiller, Francesca Farias, Kelly Soares de Sales, Igor Rafael Praxedes Luppi, Pierre-Hervé Ribeiro, Sidarta Queiroz, Claudio Marcos Sci Rep Article Hippocampal (HPC) theta oscillation during post-training rapid eye movement (REM) sleep supports spatial learning. Theta also modulates neuronal and oscillatory activity in the retrosplenial cortex (RSC) during REM sleep. To investigate the relevance of theta-driven interaction between these two regions to memory consolidation, we computed the Granger causality within theta range on electrophysiological data recorded in freely behaving rats during REM sleep, both before and after contextual fear conditioning. We found a training-induced modulation of causality between HPC and RSC that was correlated with memory retrieval 24 h later. Retrieval was proportional to the change in the relative influence RSC exerted upon HPC theta oscillation. Importantly, causality peaked during theta acceleration, in synchrony with phasic REM sleep. Altogether, these results support a role for phasic REM sleep in hippocampo-cortical memory consolidation and suggest that causality modulation between RSC and HPC during REM sleep plays a functional role in that phenomenon. Nature Publishing Group UK 2021-06-22 /pmc/articles/PMC8219679/ /pubmed/34158548 http://dx.doi.org/10.1038/s41598-021-91659-5 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
de Almeida-Filho, Daniel Gomes
Koike, Bruna Del Vechio
Billwiller, Francesca
Farias, Kelly Soares
de Sales, Igor Rafael Praxedes
Luppi, Pierre-Hervé
Ribeiro, Sidarta
Queiroz, Claudio Marcos
Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation
title Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation
title_full Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation
title_fullStr Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation
title_full_unstemmed Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation
title_short Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation
title_sort hippocampus-retrosplenial cortex interaction is increased during phasic rem and contributes to memory consolidation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219679/
https://www.ncbi.nlm.nih.gov/pubmed/34158548
http://dx.doi.org/10.1038/s41598-021-91659-5
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