Cargando…

Short Duration Repetitive Transcranial Electrical Stimulation During Sleep Enhances Declarative Memory of Facts

Transcranial electrical stimulation (tES) during sleep has been shown to successfully modulate memory consolidation. Here, we tested the effect of short duration repetitive tES (SDR-tES) during a daytime nap on the consolidation of declarative memory of facts in healthy individuals. We use a previou...

Descripción completa

Detalles Bibliográficos
Autores principales: Cellini, Nicola, Shimizu, Renee E., Connolly, Patrick M., Armstrong, Diana M., Hernandez, Lexus T., Polakiewicz, Anthony G., Estrada, Rolando, Aguilar-Simon, Mario, Weisend, Michael P., Mednick, Sara C., Simons, Stephen B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474382/
https://www.ncbi.nlm.nih.gov/pubmed/31031612
http://dx.doi.org/10.3389/fnhum.2019.00123
_version_ 1783412623799222272
author Cellini, Nicola
Shimizu, Renee E.
Connolly, Patrick M.
Armstrong, Diana M.
Hernandez, Lexus T.
Polakiewicz, Anthony G.
Estrada, Rolando
Aguilar-Simon, Mario
Weisend, Michael P.
Mednick, Sara C.
Simons, Stephen B.
author_facet Cellini, Nicola
Shimizu, Renee E.
Connolly, Patrick M.
Armstrong, Diana M.
Hernandez, Lexus T.
Polakiewicz, Anthony G.
Estrada, Rolando
Aguilar-Simon, Mario
Weisend, Michael P.
Mednick, Sara C.
Simons, Stephen B.
author_sort Cellini, Nicola
collection PubMed
description Transcranial electrical stimulation (tES) during sleep has been shown to successfully modulate memory consolidation. Here, we tested the effect of short duration repetitive tES (SDR-tES) during a daytime nap on the consolidation of declarative memory of facts in healthy individuals. We use a previously described approach to deliver the stimulation at regular intervals during non-rapid eye movement (NREM) sleep, specifically stage NREM2 and NREM3. Similar to previous studies using tES, we find enhanced memory performance compared to sham both after sleep and 48 h later. We also observed an increase in the proportion of time spent in NREM3 sleep and SDR-tES boosted the overall rate of slow oscillations (SOs) during NREM2/NREM3 sleep. Retrospective investigation of brain activity immediately preceding stimulation suggests that increases in the SO rate are more likely when stimulation is delivered during quiescent and asynchronous periods of activity in contrast to other closed-loop approaches which target phasic stimulation during ongoing SOs.
format Online
Article
Text
id pubmed-6474382
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-64743822019-04-26 Short Duration Repetitive Transcranial Electrical Stimulation During Sleep Enhances Declarative Memory of Facts Cellini, Nicola Shimizu, Renee E. Connolly, Patrick M. Armstrong, Diana M. Hernandez, Lexus T. Polakiewicz, Anthony G. Estrada, Rolando Aguilar-Simon, Mario Weisend, Michael P. Mednick, Sara C. Simons, Stephen B. Front Hum Neurosci Neuroscience Transcranial electrical stimulation (tES) during sleep has been shown to successfully modulate memory consolidation. Here, we tested the effect of short duration repetitive tES (SDR-tES) during a daytime nap on the consolidation of declarative memory of facts in healthy individuals. We use a previously described approach to deliver the stimulation at regular intervals during non-rapid eye movement (NREM) sleep, specifically stage NREM2 and NREM3. Similar to previous studies using tES, we find enhanced memory performance compared to sham both after sleep and 48 h later. We also observed an increase in the proportion of time spent in NREM3 sleep and SDR-tES boosted the overall rate of slow oscillations (SOs) during NREM2/NREM3 sleep. Retrospective investigation of brain activity immediately preceding stimulation suggests that increases in the SO rate are more likely when stimulation is delivered during quiescent and asynchronous periods of activity in contrast to other closed-loop approaches which target phasic stimulation during ongoing SOs. Frontiers Media S.A. 2019-04-12 /pmc/articles/PMC6474382/ /pubmed/31031612 http://dx.doi.org/10.3389/fnhum.2019.00123 Text en Copyright © 2019 Cellini, Shimizu, Connolly, Armstrong, Hernandez, Polakiewicz, Estrada, Aguilar-Simon, Weisend, Mednick and Simons. 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
Cellini, Nicola
Shimizu, Renee E.
Connolly, Patrick M.
Armstrong, Diana M.
Hernandez, Lexus T.
Polakiewicz, Anthony G.
Estrada, Rolando
Aguilar-Simon, Mario
Weisend, Michael P.
Mednick, Sara C.
Simons, Stephen B.
Short Duration Repetitive Transcranial Electrical Stimulation During Sleep Enhances Declarative Memory of Facts
title Short Duration Repetitive Transcranial Electrical Stimulation During Sleep Enhances Declarative Memory of Facts
title_full Short Duration Repetitive Transcranial Electrical Stimulation During Sleep Enhances Declarative Memory of Facts
title_fullStr Short Duration Repetitive Transcranial Electrical Stimulation During Sleep Enhances Declarative Memory of Facts
title_full_unstemmed Short Duration Repetitive Transcranial Electrical Stimulation During Sleep Enhances Declarative Memory of Facts
title_short Short Duration Repetitive Transcranial Electrical Stimulation During Sleep Enhances Declarative Memory of Facts
title_sort short duration repetitive transcranial electrical stimulation during sleep enhances declarative memory of facts
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474382/
https://www.ncbi.nlm.nih.gov/pubmed/31031612
http://dx.doi.org/10.3389/fnhum.2019.00123
work_keys_str_mv AT cellininicola shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT shimizureneee shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT connollypatrickm shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT armstrongdianam shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT hernandezlexust shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT polakiewiczanthonyg shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT estradarolando shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT aguilarsimonmario shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT weisendmichaelp shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT mednicksarac shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts
AT simonsstephenb shortdurationrepetitivetranscranialelectricalstimulationduringsleepenhancesdeclarativememoryoffacts