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

Detalhes bibliográficos
Autor(a) principal: Almeida Filho, Daniel Gomes de
Data de Publicação: 2021
Outros Autores: Koike, Bruna Del Vechio, Billwiller, Francesca, Farias, Kelly Soares, Sales, Igor Rafael Praxedes de, Luppi, Pierre-Hervé, Ribeiro, Sidarta Tollendal Gomes, Queiroz, Claudio Marcos Teixeira de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/handle/123456789/32768
Resumo: 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 Almeida Filho, Daniel Gomes deKoike, Bruna Del VechioBillwiller, FrancescaFarias, Kelly SoaresSales, Igor Rafael Praxedes deLuppi, Pierre-HervéRibeiro, Sidarta Tollendal GomesQueiroz, Claudio Marcos Teixeira de2021-06-24T12:39:09Z2021-06-24T12:39:09Z2021-06-22ALMEIDA-FILHO, Daniel Gomes de; KOIKE, Bruna del Vechio; BILLWILLER, Francesca; FARIAS, Kelly Soares; SALES, Igor Rafael Praxedes de; LUPPI, Pierre-Hervé; RIBEIRO, Sidarta; QUEIROZ, Claudio Marcos. Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation. Scientific Reports, [S. l.], v. 11, n. 1, p. 13078. jun. 2021. Doi: http://dx.doi.org/10.1038/s41598-021-91659-5. Disponível em: https://www.nature.com/articles/s41598-021-91659-5. Acesso em: 24 jun. 2021.https://repositorio.ufrn.br/handle/123456789/3276810.1038/s41598-021-91659-5Springer Science and Business Media LLCAttribution 3.0 Brazilhttp://creativecommons.org/licenses/by/3.0/br/info:eu-repo/semantics/openAccessHippocampusTheta rhythmSleep, REMSpatial learningGyrus cinguliHippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidationinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleHippocampal (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 phenomenonengreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNORIGINALHippocampus‑retrosplenialCortex_Queiroz_2021.pdfHippocampus‑retrosplenialCortex_Queiroz_2021.pdfHippocampus‑retrosplenialCortex_Queiroz_2021application/pdf2985296https://repositorio.ufrn.br/bitstream/123456789/32768/1/Hippocampus%e2%80%91retrosplenialCortex_Queiroz_2021.pdf04efac4a271d701071fc853d2072d25cMD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8914https://repositorio.ufrn.br/bitstream/123456789/32768/2/license_rdf4d2950bda3d176f570a9f8b328dfbbefMD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81484https://repositorio.ufrn.br/bitstream/123456789/32768/3/license.txte9597aa2854d128fd968be5edc8a28d9MD53123456789/327682021-06-24 09:39:10.5oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2021-06-24T12:39:10Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.pt_BR.fl_str_mv 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
spellingShingle Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation
Almeida Filho, Daniel Gomes de
Hippocampus
Theta rhythm
Sleep, REM
Spatial learning
Gyrus cinguli
title_short 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_sort Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation
author Almeida Filho, Daniel Gomes de
author_facet Almeida Filho, Daniel Gomes de
Koike, Bruna Del Vechio
Billwiller, Francesca
Farias, Kelly Soares
Sales, Igor Rafael Praxedes de
Luppi, Pierre-Hervé
Ribeiro, Sidarta Tollendal Gomes
Queiroz, Claudio Marcos Teixeira de
author_role author
author2 Koike, Bruna Del Vechio
Billwiller, Francesca
Farias, Kelly Soares
Sales, Igor Rafael Praxedes de
Luppi, Pierre-Hervé
Ribeiro, Sidarta Tollendal Gomes
Queiroz, Claudio Marcos Teixeira de
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Almeida Filho, Daniel Gomes de
Koike, Bruna Del Vechio
Billwiller, Francesca
Farias, Kelly Soares
Sales, Igor Rafael Praxedes de
Luppi, Pierre-Hervé
Ribeiro, Sidarta Tollendal Gomes
Queiroz, Claudio Marcos Teixeira de
dc.subject.por.fl_str_mv Hippocampus
Theta rhythm
Sleep, REM
Spatial learning
Gyrus cinguli
topic Hippocampus
Theta rhythm
Sleep, REM
Spatial learning
Gyrus cinguli
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
publishDate 2021
dc.date.accessioned.fl_str_mv 2021-06-24T12:39:09Z
dc.date.available.fl_str_mv 2021-06-24T12:39:09Z
dc.date.issued.fl_str_mv 2021-06-22
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.citation.fl_str_mv ALMEIDA-FILHO, Daniel Gomes de; KOIKE, Bruna del Vechio; BILLWILLER, Francesca; FARIAS, Kelly Soares; SALES, Igor Rafael Praxedes de; LUPPI, Pierre-Hervé; RIBEIRO, Sidarta; QUEIROZ, Claudio Marcos. Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation. Scientific Reports, [S. l.], v. 11, n. 1, p. 13078. jun. 2021. Doi: http://dx.doi.org/10.1038/s41598-021-91659-5. Disponível em: https://www.nature.com/articles/s41598-021-91659-5. Acesso em: 24 jun. 2021.
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/handle/123456789/32768
dc.identifier.doi.none.fl_str_mv 10.1038/s41598-021-91659-5
identifier_str_mv ALMEIDA-FILHO, Daniel Gomes de; KOIKE, Bruna del Vechio; BILLWILLER, Francesca; FARIAS, Kelly Soares; SALES, Igor Rafael Praxedes de; LUPPI, Pierre-Hervé; RIBEIRO, Sidarta; QUEIROZ, Claudio Marcos. Hippocampus-retrosplenial cortex interaction is increased during phasic REM and contributes to memory consolidation. Scientific Reports, [S. l.], v. 11, n. 1, p. 13078. jun. 2021. Doi: http://dx.doi.org/10.1038/s41598-021-91659-5. Disponível em: https://www.nature.com/articles/s41598-021-91659-5. Acesso em: 24 jun. 2021.
10.1038/s41598-021-91659-5
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http://creativecommons.org/licenses/by/3.0/br/
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