Cargando…

Rehearsal initiates systems memory consolidation, sleep makes it last

After encoding, memories undergo a transitional process termed systems memory consolidation. It allows fast acquisition of new information by the hippocampus, as well as stable storage in neocortical long-term networks, where memory is protected from interference. Whereas this process is generally t...

Descripción completa

Detalles Bibliográficos
Autores principales: Himmer, L., Schönauer, M., Heib, D. P. J., Schabus, M., Gais, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482015/
https://www.ncbi.nlm.nih.gov/pubmed/31032406
http://dx.doi.org/10.1126/sciadv.aav1695
_version_ 1783413820365996032
author Himmer, L.
Schönauer, M.
Heib, D. P. J.
Schabus, M.
Gais, S.
author_facet Himmer, L.
Schönauer, M.
Heib, D. P. J.
Schabus, M.
Gais, S.
author_sort Himmer, L.
collection PubMed
description After encoding, memories undergo a transitional process termed systems memory consolidation. It allows fast acquisition of new information by the hippocampus, as well as stable storage in neocortical long-term networks, where memory is protected from interference. Whereas this process is generally thought to occur slowly over time and sleep, we recently found a rapid memory systems transition from hippocampus to posterior parietal cortex (PPC) that occurs over repeated rehearsal within one study session. Here, we use fMRI to demonstrate that this transition is stabilized over sleep, whereas wakefulness leads to a reset to naïve responses, such as observed during early encoding. The role of sleep therefore seems to go beyond providing additional rehearsal through memory trace reactivation, as previously thought. We conclude that repeated study induces systems consolidation, while sleep ensures that these transformations become stable and long lasting. Thus, sleep and repeated rehearsal jointly contribute to long-term memory consolidation.
format Online
Article
Text
id pubmed-6482015
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-64820152019-04-26 Rehearsal initiates systems memory consolidation, sleep makes it last Himmer, L. Schönauer, M. Heib, D. P. J. Schabus, M. Gais, S. Sci Adv Research Articles After encoding, memories undergo a transitional process termed systems memory consolidation. It allows fast acquisition of new information by the hippocampus, as well as stable storage in neocortical long-term networks, where memory is protected from interference. Whereas this process is generally thought to occur slowly over time and sleep, we recently found a rapid memory systems transition from hippocampus to posterior parietal cortex (PPC) that occurs over repeated rehearsal within one study session. Here, we use fMRI to demonstrate that this transition is stabilized over sleep, whereas wakefulness leads to a reset to naïve responses, such as observed during early encoding. The role of sleep therefore seems to go beyond providing additional rehearsal through memory trace reactivation, as previously thought. We conclude that repeated study induces systems consolidation, while sleep ensures that these transformations become stable and long lasting. Thus, sleep and repeated rehearsal jointly contribute to long-term memory consolidation. American Association for the Advancement of Science 2019-04-24 /pmc/articles/PMC6482015/ /pubmed/31032406 http://dx.doi.org/10.1126/sciadv.aav1695 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Himmer, L.
Schönauer, M.
Heib, D. P. J.
Schabus, M.
Gais, S.
Rehearsal initiates systems memory consolidation, sleep makes it last
title Rehearsal initiates systems memory consolidation, sleep makes it last
title_full Rehearsal initiates systems memory consolidation, sleep makes it last
title_fullStr Rehearsal initiates systems memory consolidation, sleep makes it last
title_full_unstemmed Rehearsal initiates systems memory consolidation, sleep makes it last
title_short Rehearsal initiates systems memory consolidation, sleep makes it last
title_sort rehearsal initiates systems memory consolidation, sleep makes it last
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482015/
https://www.ncbi.nlm.nih.gov/pubmed/31032406
http://dx.doi.org/10.1126/sciadv.aav1695
work_keys_str_mv AT himmerl rehearsalinitiatessystemsmemoryconsolidationsleepmakesitlast
AT schonauerm rehearsalinitiatessystemsmemoryconsolidationsleepmakesitlast
AT heibdpj rehearsalinitiatessystemsmemoryconsolidationsleepmakesitlast
AT schabusm rehearsalinitiatessystemsmemoryconsolidationsleepmakesitlast
AT gaiss rehearsalinitiatessystemsmemoryconsolidationsleepmakesitlast