Visuomotor Adaptation Modulates the Clustering of Sleep Spindles Into Trains

Sleep spindles are thought to promote memory consolidation. Recently, we have shown that visuomotor adaptation (VMA) learning increases the density of spindles and promotes the coupling between spindles and slow oscillations, locally, with the level of spindle-SO synchrony predicting overnight memor...

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Main Authors: Agustín Solano, Luis A. Riquelme, Daniel Perez-Chada, Valeria Della-Maggiore
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-03-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2022.803387/full
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author Agustín Solano
Luis A. Riquelme
Daniel Perez-Chada
Valeria Della-Maggiore
author_facet Agustín Solano
Luis A. Riquelme
Daniel Perez-Chada
Valeria Della-Maggiore
author_sort Agustín Solano
collection DOAJ
description Sleep spindles are thought to promote memory consolidation. Recently, we have shown that visuomotor adaptation (VMA) learning increases the density of spindles and promotes the coupling between spindles and slow oscillations, locally, with the level of spindle-SO synchrony predicting overnight memory retention. Yet, growing evidence suggests that the rhythmicity in spindle occurrence may also influence the stabilization of declarative and procedural memories. Here, we examined if VMA learning promotes the temporal organization of sleep spindles into trains. We found that VMA increased the proportion of spindles and spindle-SO couplings in trains. In agreement with our previous work, this modulation was observed over the contralateral hemisphere to the trained hand, and predicted overnight memory retention. Interestingly, spindles grouped in a cluster showed greater amplitude and duration than isolated spindles. The fact that these features increased as a function of train length, provides evidence supporting a biological advantage of this temporal arrangement. Our work opens the possibility that the periodicity of NREM oscillations may be relevant in the stabilization of procedural memories.
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spelling doaj.art-be2b234b154046bbab5428bd8eff55d02022-12-21T19:27:30ZengFrontiers Media S.A.Frontiers in Neuroscience1662-453X2022-03-011610.3389/fnins.2022.803387803387Visuomotor Adaptation Modulates the Clustering of Sleep Spindles Into TrainsAgustín Solano0Luis A. Riquelme1Daniel Perez-Chada2Valeria Della-Maggiore3IFIBIO Houssay, Department of Physiology, School of Medicine, University of Buenos Aires, Buenos Aires, ArgentinaIFIBIO Houssay, Department of Physiology, School of Medicine, University of Buenos Aires, Buenos Aires, ArgentinaDepartment of Internal Medicine, Pulmonary and Sleep Medicine Service, Austral University Hospital, Buenos Aires, ArgentinaIFIBIO Houssay, Department of Physiology, School of Medicine, University of Buenos Aires, Buenos Aires, ArgentinaSleep spindles are thought to promote memory consolidation. Recently, we have shown that visuomotor adaptation (VMA) learning increases the density of spindles and promotes the coupling between spindles and slow oscillations, locally, with the level of spindle-SO synchrony predicting overnight memory retention. Yet, growing evidence suggests that the rhythmicity in spindle occurrence may also influence the stabilization of declarative and procedural memories. Here, we examined if VMA learning promotes the temporal organization of sleep spindles into trains. We found that VMA increased the proportion of spindles and spindle-SO couplings in trains. In agreement with our previous work, this modulation was observed over the contralateral hemisphere to the trained hand, and predicted overnight memory retention. Interestingly, spindles grouped in a cluster showed greater amplitude and duration than isolated spindles. The fact that these features increased as a function of train length, provides evidence supporting a biological advantage of this temporal arrangement. Our work opens the possibility that the periodicity of NREM oscillations may be relevant in the stabilization of procedural memories.https://www.frontiersin.org/articles/10.3389/fnins.2022.803387/fullhumanmotor learningsleepspindle trainslow oscillation
spellingShingle Agustín Solano
Luis A. Riquelme
Daniel Perez-Chada
Valeria Della-Maggiore
Visuomotor Adaptation Modulates the Clustering of Sleep Spindles Into Trains
Frontiers in Neuroscience
human
motor learning
sleep
spindle train
slow oscillation
title Visuomotor Adaptation Modulates the Clustering of Sleep Spindles Into Trains
title_full Visuomotor Adaptation Modulates the Clustering of Sleep Spindles Into Trains
title_fullStr Visuomotor Adaptation Modulates the Clustering of Sleep Spindles Into Trains
title_full_unstemmed Visuomotor Adaptation Modulates the Clustering of Sleep Spindles Into Trains
title_short Visuomotor Adaptation Modulates the Clustering of Sleep Spindles Into Trains
title_sort visuomotor adaptation modulates the clustering of sleep spindles into trains
topic human
motor learning
sleep
spindle train
slow oscillation
url https://www.frontiersin.org/articles/10.3389/fnins.2022.803387/full
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AT danielperezchada visuomotoradaptationmodulatestheclusteringofsleepspindlesintotrains
AT valeriadellamaggiore visuomotoradaptationmodulatestheclusteringofsleepspindlesintotrains