Cargando…
The human thalamus orchestrates neocortical oscillations during NREM sleep
A hallmark of non-rapid eye movement sleep is the coordinated interplay of slow oscillations (SOs) and sleep spindles. Traditionally, a cortico-thalamo-cortical loop is suggested to coordinate these rhythms: neocortically-generated SOs trigger spindles in the thalamus that are projected back to neoc...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445182/ https://www.ncbi.nlm.nih.gov/pubmed/36064855 http://dx.doi.org/10.1038/s41467-022-32840-w |
_version_ | 1784783370725621760 |
---|---|
author | Schreiner, Thomas Kaufmann, Elisabeth Noachtar, Soheyl Mehrkens, Jan-Hinnerk Staudigl, Tobias |
author_facet | Schreiner, Thomas Kaufmann, Elisabeth Noachtar, Soheyl Mehrkens, Jan-Hinnerk Staudigl, Tobias |
author_sort | Schreiner, Thomas |
collection | PubMed |
description | A hallmark of non-rapid eye movement sleep is the coordinated interplay of slow oscillations (SOs) and sleep spindles. Traditionally, a cortico-thalamo-cortical loop is suggested to coordinate these rhythms: neocortically-generated SOs trigger spindles in the thalamus that are projected back to neocortex. Here, we used intrathalamic recordings from human epilepsy patients to test this canonical interplay. We show that SOs in the anterior thalamus precede neocortical SOs (peak −50 ms), whereas concurrently-recorded SOs in the mediodorsal thalamus are led by neocortical SOs (peak +50 ms). Sleep spindles, detected in both thalamic nuclei, preceded their neocortical counterparts (peak −100 ms) and were initiated during early phases of thalamic SOs. Our findings indicate an active role of the anterior thalamus in organizing sleep rhythms in the neocortex and highlight the functional diversity of thalamic nuclei in humans. The thalamic coordination of sleep oscillations could have broad implications for the mechanisms underlying memory consolidation. |
format | Online Article Text |
id | pubmed-9445182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-94451822022-09-07 The human thalamus orchestrates neocortical oscillations during NREM sleep Schreiner, Thomas Kaufmann, Elisabeth Noachtar, Soheyl Mehrkens, Jan-Hinnerk Staudigl, Tobias Nat Commun Article A hallmark of non-rapid eye movement sleep is the coordinated interplay of slow oscillations (SOs) and sleep spindles. Traditionally, a cortico-thalamo-cortical loop is suggested to coordinate these rhythms: neocortically-generated SOs trigger spindles in the thalamus that are projected back to neocortex. Here, we used intrathalamic recordings from human epilepsy patients to test this canonical interplay. We show that SOs in the anterior thalamus precede neocortical SOs (peak −50 ms), whereas concurrently-recorded SOs in the mediodorsal thalamus are led by neocortical SOs (peak +50 ms). Sleep spindles, detected in both thalamic nuclei, preceded their neocortical counterparts (peak −100 ms) and were initiated during early phases of thalamic SOs. Our findings indicate an active role of the anterior thalamus in organizing sleep rhythms in the neocortex and highlight the functional diversity of thalamic nuclei in humans. The thalamic coordination of sleep oscillations could have broad implications for the mechanisms underlying memory consolidation. Nature Publishing Group UK 2022-09-05 /pmc/articles/PMC9445182/ /pubmed/36064855 http://dx.doi.org/10.1038/s41467-022-32840-w Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Schreiner, Thomas Kaufmann, Elisabeth Noachtar, Soheyl Mehrkens, Jan-Hinnerk Staudigl, Tobias The human thalamus orchestrates neocortical oscillations during NREM sleep |
title | The human thalamus orchestrates neocortical oscillations during NREM sleep |
title_full | The human thalamus orchestrates neocortical oscillations during NREM sleep |
title_fullStr | The human thalamus orchestrates neocortical oscillations during NREM sleep |
title_full_unstemmed | The human thalamus orchestrates neocortical oscillations during NREM sleep |
title_short | The human thalamus orchestrates neocortical oscillations during NREM sleep |
title_sort | human thalamus orchestrates neocortical oscillations during nrem sleep |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445182/ https://www.ncbi.nlm.nih.gov/pubmed/36064855 http://dx.doi.org/10.1038/s41467-022-32840-w |
work_keys_str_mv | AT schreinerthomas thehumanthalamusorchestratesneocorticaloscillationsduringnremsleep AT kaufmannelisabeth thehumanthalamusorchestratesneocorticaloscillationsduringnremsleep AT noachtarsoheyl thehumanthalamusorchestratesneocorticaloscillationsduringnremsleep AT mehrkensjanhinnerk thehumanthalamusorchestratesneocorticaloscillationsduringnremsleep AT staudigltobias thehumanthalamusorchestratesneocorticaloscillationsduringnremsleep AT schreinerthomas humanthalamusorchestratesneocorticaloscillationsduringnremsleep AT kaufmannelisabeth humanthalamusorchestratesneocorticaloscillationsduringnremsleep AT noachtarsoheyl humanthalamusorchestratesneocorticaloscillationsduringnremsleep AT mehrkensjanhinnerk humanthalamusorchestratesneocorticaloscillationsduringnremsleep AT staudigltobias humanthalamusorchestratesneocorticaloscillationsduringnremsleep |