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Spatiotemporal Dynamics of Sleep Spindle Sources Across NREM Sleep Cycles

The existence of two different types of sleep spindles (slow and fast) is well-established, according to their topographical distribution at scalp- and cortical-level. Our aim was to provide a systematic investigation focused on the temporal evolution of sleep spindle sources during non-rapid eye mo...

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Autores principales: Alfonsi, Valentina, D’Atri, Aurora, Gorgoni, Maurizio, Scarpelli, Serena, Mangiaruga, Anastasia, Ferrara, Michele, De Gennaro, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635592/
https://www.ncbi.nlm.nih.gov/pubmed/31354426
http://dx.doi.org/10.3389/fnins.2019.00727
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author Alfonsi, Valentina
D’Atri, Aurora
Gorgoni, Maurizio
Scarpelli, Serena
Mangiaruga, Anastasia
Ferrara, Michele
De Gennaro, Luigi
author_facet Alfonsi, Valentina
D’Atri, Aurora
Gorgoni, Maurizio
Scarpelli, Serena
Mangiaruga, Anastasia
Ferrara, Michele
De Gennaro, Luigi
author_sort Alfonsi, Valentina
collection PubMed
description The existence of two different types of sleep spindles (slow and fast) is well-established, according to their topographical distribution at scalp- and cortical-level. Our aim was to provide a systematic investigation focused on the temporal evolution of sleep spindle sources during non-rapid eye movement (NREM) sleep. Spindle activity was recorded and automatically detected in 20 healthy subjects. Low resolution brain electromagnetic tomography (LORETA) was applied for the EEG source localization. Aiming to evaluate the time course of the detected slow and fast spindle sources, we considered the first four NREM sleep cycles and divided each cycle into five intervals of equal duration. We confirmed the preferential localization in the frontal (Brodmann area 10) and parietal (Brodmann area 7) cortical regions, respectively for slow (11.0–12.5) and fast (13.0–14.5) spindles. Across subsequent NREM sleep episodes, the maximal source activation remained systematically located in Brodmann area 10 and Brodmann area 7, showing the topographical stability of the detected generators. However, a different time course was observed as a function of the type of spindles: a linear decrease across subsequent cycles was found for slow spindle but not for fast spindle source. The intra-cycle variations followed a “U” shaped curve for both spindle source, with a trough around third and fourth interval (middle part) and the highest values at the beginning and the end of the considered temporal window. We confirmed the involvement of the frontal and parietal brain regions in spindle generation, showing for the first time their changes within and between consecutive NREM sleep episodes. Our results point to a correspondence between the scalp-recorded electrical activity and the underlying source topography, supporting the notion that spindles are not uniform phenomena: complex region- and time-specific patterns are involved in their generation and manifestation.
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spelling pubmed-66355922019-07-26 Spatiotemporal Dynamics of Sleep Spindle Sources Across NREM Sleep Cycles Alfonsi, Valentina D’Atri, Aurora Gorgoni, Maurizio Scarpelli, Serena Mangiaruga, Anastasia Ferrara, Michele De Gennaro, Luigi Front Neurosci Neuroscience The existence of two different types of sleep spindles (slow and fast) is well-established, according to their topographical distribution at scalp- and cortical-level. Our aim was to provide a systematic investigation focused on the temporal evolution of sleep spindle sources during non-rapid eye movement (NREM) sleep. Spindle activity was recorded and automatically detected in 20 healthy subjects. Low resolution brain electromagnetic tomography (LORETA) was applied for the EEG source localization. Aiming to evaluate the time course of the detected slow and fast spindle sources, we considered the first four NREM sleep cycles and divided each cycle into five intervals of equal duration. We confirmed the preferential localization in the frontal (Brodmann area 10) and parietal (Brodmann area 7) cortical regions, respectively for slow (11.0–12.5) and fast (13.0–14.5) spindles. Across subsequent NREM sleep episodes, the maximal source activation remained systematically located in Brodmann area 10 and Brodmann area 7, showing the topographical stability of the detected generators. However, a different time course was observed as a function of the type of spindles: a linear decrease across subsequent cycles was found for slow spindle but not for fast spindle source. The intra-cycle variations followed a “U” shaped curve for both spindle source, with a trough around third and fourth interval (middle part) and the highest values at the beginning and the end of the considered temporal window. We confirmed the involvement of the frontal and parietal brain regions in spindle generation, showing for the first time their changes within and between consecutive NREM sleep episodes. Our results point to a correspondence between the scalp-recorded electrical activity and the underlying source topography, supporting the notion that spindles are not uniform phenomena: complex region- and time-specific patterns are involved in their generation and manifestation. Frontiers Media S.A. 2019-07-10 /pmc/articles/PMC6635592/ /pubmed/31354426 http://dx.doi.org/10.3389/fnins.2019.00727 Text en Copyright © 2019 Alfonsi, D’Atri, Gorgoni, Scarpelli, Mangiaruga, Ferrara and De Gennaro. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Alfonsi, Valentina
D’Atri, Aurora
Gorgoni, Maurizio
Scarpelli, Serena
Mangiaruga, Anastasia
Ferrara, Michele
De Gennaro, Luigi
Spatiotemporal Dynamics of Sleep Spindle Sources Across NREM Sleep Cycles
title Spatiotemporal Dynamics of Sleep Spindle Sources Across NREM Sleep Cycles
title_full Spatiotemporal Dynamics of Sleep Spindle Sources Across NREM Sleep Cycles
title_fullStr Spatiotemporal Dynamics of Sleep Spindle Sources Across NREM Sleep Cycles
title_full_unstemmed Spatiotemporal Dynamics of Sleep Spindle Sources Across NREM Sleep Cycles
title_short Spatiotemporal Dynamics of Sleep Spindle Sources Across NREM Sleep Cycles
title_sort spatiotemporal dynamics of sleep spindle sources across nrem sleep cycles
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635592/
https://www.ncbi.nlm.nih.gov/pubmed/31354426
http://dx.doi.org/10.3389/fnins.2019.00727
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