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Distinct dynamics of neuronal activity during concurrent motor planning and execution

The smooth conduct of movements requires simultaneous motor planning and execution according to internal goals. So far it remains unknown how such movement plans are modified without interfering with ongoing movements. Previous studies have isolated planning and execution-related neuronal activity b...

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Autores principales: Eriksson, David, Heiland, Mona, Schneider, Artur, Diester, Ilka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433382/
https://www.ncbi.nlm.nih.gov/pubmed/34508073
http://dx.doi.org/10.1038/s41467-021-25558-8
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author Eriksson, David
Heiland, Mona
Schneider, Artur
Diester, Ilka
author_facet Eriksson, David
Heiland, Mona
Schneider, Artur
Diester, Ilka
author_sort Eriksson, David
collection PubMed
description The smooth conduct of movements requires simultaneous motor planning and execution according to internal goals. So far it remains unknown how such movement plans are modified without interfering with ongoing movements. Previous studies have isolated planning and execution-related neuronal activity by separating behavioral planning and movement periods in time by sensory cues. Here, we separate continuous self-paced motor planning from motor execution statistically, by experimentally minimizing the repetitiveness of the movements. This approach shows that, in the rat sensorimotor cortex, neuronal motor planning processes evolve with slower dynamics than movement-related responses. Fast-evolving neuronal activity precees skilled forelimb movements and is nested within slower dynamics. We capture this effect via high-pass filtering and confirm the results with optogenetic stimulations. The various dynamics combined with adaptation-based high-pass filtering provide a simple principle for separating concurrent motor planning and execution.
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spelling pubmed-84333822021-09-24 Distinct dynamics of neuronal activity during concurrent motor planning and execution Eriksson, David Heiland, Mona Schneider, Artur Diester, Ilka Nat Commun Article The smooth conduct of movements requires simultaneous motor planning and execution according to internal goals. So far it remains unknown how such movement plans are modified without interfering with ongoing movements. Previous studies have isolated planning and execution-related neuronal activity by separating behavioral planning and movement periods in time by sensory cues. Here, we separate continuous self-paced motor planning from motor execution statistically, by experimentally minimizing the repetitiveness of the movements. This approach shows that, in the rat sensorimotor cortex, neuronal motor planning processes evolve with slower dynamics than movement-related responses. Fast-evolving neuronal activity precees skilled forelimb movements and is nested within slower dynamics. We capture this effect via high-pass filtering and confirm the results with optogenetic stimulations. The various dynamics combined with adaptation-based high-pass filtering provide a simple principle for separating concurrent motor planning and execution. Nature Publishing Group UK 2021-09-10 /pmc/articles/PMC8433382/ /pubmed/34508073 http://dx.doi.org/10.1038/s41467-021-25558-8 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 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
Eriksson, David
Heiland, Mona
Schneider, Artur
Diester, Ilka
Distinct dynamics of neuronal activity during concurrent motor planning and execution
title Distinct dynamics of neuronal activity during concurrent motor planning and execution
title_full Distinct dynamics of neuronal activity during concurrent motor planning and execution
title_fullStr Distinct dynamics of neuronal activity during concurrent motor planning and execution
title_full_unstemmed Distinct dynamics of neuronal activity during concurrent motor planning and execution
title_short Distinct dynamics of neuronal activity during concurrent motor planning and execution
title_sort distinct dynamics of neuronal activity during concurrent motor planning and execution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433382/
https://www.ncbi.nlm.nih.gov/pubmed/34508073
http://dx.doi.org/10.1038/s41467-021-25558-8
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