Cargando…

Phase-based coordination of hippocampal and neocortical oscillations during human sleep

During sleep, new memories undergo a gradual transfer from hippocampal (HPC) to neocortical (NC) sites. Precisely timed neural oscillations are thought to mediate this sleep-dependent memory consolidation, but exactly how sleep oscillations instantiate the HPC-NC dialog remains elusive. Employing ov...

Descripción completa

Detalles Bibliográficos
Autores principales: Cox, Roy, Rüber, Theodor, Staresina, Bernhard P., Fell, Juergen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170909/
https://www.ncbi.nlm.nih.gov/pubmed/32313064
http://dx.doi.org/10.1038/s42003-020-0913-5
_version_ 1783523971866558464
author Cox, Roy
Rüber, Theodor
Staresina, Bernhard P.
Fell, Juergen
author_facet Cox, Roy
Rüber, Theodor
Staresina, Bernhard P.
Fell, Juergen
author_sort Cox, Roy
collection PubMed
description During sleep, new memories undergo a gradual transfer from hippocampal (HPC) to neocortical (NC) sites. Precisely timed neural oscillations are thought to mediate this sleep-dependent memory consolidation, but exactly how sleep oscillations instantiate the HPC-NC dialog remains elusive. Employing overnight invasive electroencephalography in ten neurosurgical patients, we identified three broad classes of phase-based communication between HPC and lateral temporal NC. First, we observed interregional phase synchrony for non-rapid eye movement (NREM) spindles, and N2 and rapid eye movement (REM) theta activity. Second, we found asymmetrical N3 cross-frequency phase-amplitude coupling between HPC slow oscillations (SOs) and NC activity spanning the delta to high-gamma/ripple bands, but not in the opposite direction. Lastly, N2 theta and NREM spindle synchrony were themselves modulated by HPC SOs. These forms of interregional communication emphasize the role of HPC SOs in the HPC-NC dialog, and may offer a physiological basis for the sleep-dependent reorganization of mnemonic content.
format Online
Article
Text
id pubmed-7170909
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-71709092020-04-29 Phase-based coordination of hippocampal and neocortical oscillations during human sleep Cox, Roy Rüber, Theodor Staresina, Bernhard P. Fell, Juergen Commun Biol Article During sleep, new memories undergo a gradual transfer from hippocampal (HPC) to neocortical (NC) sites. Precisely timed neural oscillations are thought to mediate this sleep-dependent memory consolidation, but exactly how sleep oscillations instantiate the HPC-NC dialog remains elusive. Employing overnight invasive electroencephalography in ten neurosurgical patients, we identified three broad classes of phase-based communication between HPC and lateral temporal NC. First, we observed interregional phase synchrony for non-rapid eye movement (NREM) spindles, and N2 and rapid eye movement (REM) theta activity. Second, we found asymmetrical N3 cross-frequency phase-amplitude coupling between HPC slow oscillations (SOs) and NC activity spanning the delta to high-gamma/ripple bands, but not in the opposite direction. Lastly, N2 theta and NREM spindle synchrony were themselves modulated by HPC SOs. These forms of interregional communication emphasize the role of HPC SOs in the HPC-NC dialog, and may offer a physiological basis for the sleep-dependent reorganization of mnemonic content. Nature Publishing Group UK 2020-04-20 /pmc/articles/PMC7170909/ /pubmed/32313064 http://dx.doi.org/10.1038/s42003-020-0913-5 Text en © The Author(s) 2020 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
Cox, Roy
Rüber, Theodor
Staresina, Bernhard P.
Fell, Juergen
Phase-based coordination of hippocampal and neocortical oscillations during human sleep
title Phase-based coordination of hippocampal and neocortical oscillations during human sleep
title_full Phase-based coordination of hippocampal and neocortical oscillations during human sleep
title_fullStr Phase-based coordination of hippocampal and neocortical oscillations during human sleep
title_full_unstemmed Phase-based coordination of hippocampal and neocortical oscillations during human sleep
title_short Phase-based coordination of hippocampal and neocortical oscillations during human sleep
title_sort phase-based coordination of hippocampal and neocortical oscillations during human sleep
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170909/
https://www.ncbi.nlm.nih.gov/pubmed/32313064
http://dx.doi.org/10.1038/s42003-020-0913-5
work_keys_str_mv AT coxroy phasebasedcoordinationofhippocampalandneocorticaloscillationsduringhumansleep
AT rubertheodor phasebasedcoordinationofhippocampalandneocorticaloscillationsduringhumansleep
AT staresinabernhardp phasebasedcoordinationofhippocampalandneocorticaloscillationsduringhumansleep
AT felljuergen phasebasedcoordinationofhippocampalandneocorticaloscillationsduringhumansleep