Cargando…

Offline low-frequency rTMS of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability

Motor skills are acquired and refined across alternating phases of practice (online) and subsequent consolidation in the absence of further skill execution (offline). Both stages of learning are sustained by dynamic interactions within a widespread motor learning network including the premotor and p...

Descripción completa

Detalles Bibliográficos
Autores principales: Psurek, Felix, King, Bradley Ross, Classen, Joseph, Rumpf, Jost-Julian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683442/
https://www.ncbi.nlm.nih.gov/pubmed/34921224
http://dx.doi.org/10.1038/s41598-021-03737-3
_version_ 1784617419689426944
author Psurek, Felix
King, Bradley Ross
Classen, Joseph
Rumpf, Jost-Julian
author_facet Psurek, Felix
King, Bradley Ross
Classen, Joseph
Rumpf, Jost-Julian
author_sort Psurek, Felix
collection PubMed
description Motor skills are acquired and refined across alternating phases of practice (online) and subsequent consolidation in the absence of further skill execution (offline). Both stages of learning are sustained by dynamic interactions within a widespread motor learning network including the premotor and primary motor cortices. Here, we aimed to investigate the role of the dorsal premotor cortex (dPMC) and its interaction with the primary motor cortex (M1) during motor memory consolidation. Forty-eight healthy human participants (age 22.1 ± 3.1 years) were assigned to three different groups corresponding to either low-frequency (1 Hz) repetitive transcranial magnetic stimulation (rTMS) of left dPMC, rTMS of left M1, or sham rTMS. rTMS was applied immediately after explicit motor sequence training with the right hand. Motor evoked potentials were recorded before training and after rTMS to assess potential stimulation-induced changes in corticospinal excitability (CSE). Participants were retested on motor sequence performance after eight hours to assess consolidation. While rTMS of dPMC significantly increased CSE and rTMS of M1 significantly decreased CSE, no CSE modulation was induced by sham rTMS. However, all groups demonstrated similar significant offline learning indicating that consolidation was not modulated by the post-training low-frequency rTMS intervention despite evidence of an interaction of dPMC and M1 at the level of CSE. Motor memory consolidation ensuing explicit motor sequence training seems to be a rather robust process that is not affected by low-frequency rTMS-induced perturbations of dPMC or M1. Findings further indicate that consolidation of explicitly acquired motor skills is neither mediated nor reflected by post-training CSE.
format Online
Article
Text
id pubmed-8683442
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-86834422021-12-20 Offline low-frequency rTMS of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability Psurek, Felix King, Bradley Ross Classen, Joseph Rumpf, Jost-Julian Sci Rep Article Motor skills are acquired and refined across alternating phases of practice (online) and subsequent consolidation in the absence of further skill execution (offline). Both stages of learning are sustained by dynamic interactions within a widespread motor learning network including the premotor and primary motor cortices. Here, we aimed to investigate the role of the dorsal premotor cortex (dPMC) and its interaction with the primary motor cortex (M1) during motor memory consolidation. Forty-eight healthy human participants (age 22.1 ± 3.1 years) were assigned to three different groups corresponding to either low-frequency (1 Hz) repetitive transcranial magnetic stimulation (rTMS) of left dPMC, rTMS of left M1, or sham rTMS. rTMS was applied immediately after explicit motor sequence training with the right hand. Motor evoked potentials were recorded before training and after rTMS to assess potential stimulation-induced changes in corticospinal excitability (CSE). Participants were retested on motor sequence performance after eight hours to assess consolidation. While rTMS of dPMC significantly increased CSE and rTMS of M1 significantly decreased CSE, no CSE modulation was induced by sham rTMS. However, all groups demonstrated similar significant offline learning indicating that consolidation was not modulated by the post-training low-frequency rTMS intervention despite evidence of an interaction of dPMC and M1 at the level of CSE. Motor memory consolidation ensuing explicit motor sequence training seems to be a rather robust process that is not affected by low-frequency rTMS-induced perturbations of dPMC or M1. Findings further indicate that consolidation of explicitly acquired motor skills is neither mediated nor reflected by post-training CSE. Nature Publishing Group UK 2021-12-17 /pmc/articles/PMC8683442/ /pubmed/34921224 http://dx.doi.org/10.1038/s41598-021-03737-3 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Psurek, Felix
King, Bradley Ross
Classen, Joseph
Rumpf, Jost-Julian
Offline low-frequency rTMS of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability
title Offline low-frequency rTMS of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability
title_full Offline low-frequency rTMS of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability
title_fullStr Offline low-frequency rTMS of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability
title_full_unstemmed Offline low-frequency rTMS of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability
title_short Offline low-frequency rTMS of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability
title_sort offline low-frequency rtms of the primary and premotor cortices does not impact motor sequence memory consolidation despite modulation of corticospinal excitability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683442/
https://www.ncbi.nlm.nih.gov/pubmed/34921224
http://dx.doi.org/10.1038/s41598-021-03737-3
work_keys_str_mv AT psurekfelix offlinelowfrequencyrtmsoftheprimaryandpremotorcorticesdoesnotimpactmotorsequencememoryconsolidationdespitemodulationofcorticospinalexcitability
AT kingbradleyross offlinelowfrequencyrtmsoftheprimaryandpremotorcorticesdoesnotimpactmotorsequencememoryconsolidationdespitemodulationofcorticospinalexcitability
AT classenjoseph offlinelowfrequencyrtmsoftheprimaryandpremotorcorticesdoesnotimpactmotorsequencememoryconsolidationdespitemodulationofcorticospinalexcitability
AT rumpfjostjulian offlinelowfrequencyrtmsoftheprimaryandpremotorcorticesdoesnotimpactmotorsequencememoryconsolidationdespitemodulationofcorticospinalexcitability