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Motor Planning, Not Execution, Separates Motor Memories

Recent theories of limb control emphasize motor cortex as a dynamical system, with planning setting the initial neural state, and execution arising from the self-limiting evolution of the intrinsic neural dynamics. Therefore, movements that share an initial trajectory but then diverge might have dif...

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Detalles Bibliográficos
Autores principales: Sheahan, Hannah R., Franklin, David W., Wolpert, Daniel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167294/
https://www.ncbi.nlm.nih.gov/pubmed/27817979
http://dx.doi.org/10.1016/j.neuron.2016.10.017
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author Sheahan, Hannah R.
Franklin, David W.
Wolpert, Daniel M.
author_facet Sheahan, Hannah R.
Franklin, David W.
Wolpert, Daniel M.
author_sort Sheahan, Hannah R.
collection PubMed
description Recent theories of limb control emphasize motor cortex as a dynamical system, with planning setting the initial neural state, and execution arising from the self-limiting evolution of the intrinsic neural dynamics. Therefore, movements that share an initial trajectory but then diverge might have different neural states during the execution of the identical initial trajectories. We hypothesized that motor adaptation maps neural states to changes in motor command. This predicts that two opposing perturbations, which interfere when experienced over the same movement, could be learned if each is associated with a different plan even if not executed. We show that planning, but not executing, different follow-through movements allow opposing perturbations to be learned simultaneously over the same movement. However, no learning occurs if different follow throughs are executed, but not planned prior to movement initiation. Our results suggest neural, rather than physical states, are the critical factor associated with motor adaptation.
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spelling pubmed-51672942016-12-22 Motor Planning, Not Execution, Separates Motor Memories Sheahan, Hannah R. Franklin, David W. Wolpert, Daniel M. Neuron Report Recent theories of limb control emphasize motor cortex as a dynamical system, with planning setting the initial neural state, and execution arising from the self-limiting evolution of the intrinsic neural dynamics. Therefore, movements that share an initial trajectory but then diverge might have different neural states during the execution of the identical initial trajectories. We hypothesized that motor adaptation maps neural states to changes in motor command. This predicts that two opposing perturbations, which interfere when experienced over the same movement, could be learned if each is associated with a different plan even if not executed. We show that planning, but not executing, different follow-through movements allow opposing perturbations to be learned simultaneously over the same movement. However, no learning occurs if different follow throughs are executed, but not planned prior to movement initiation. Our results suggest neural, rather than physical states, are the critical factor associated with motor adaptation. Cell Press 2016-11-23 /pmc/articles/PMC5167294/ /pubmed/27817979 http://dx.doi.org/10.1016/j.neuron.2016.10.017 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Report
Sheahan, Hannah R.
Franklin, David W.
Wolpert, Daniel M.
Motor Planning, Not Execution, Separates Motor Memories
title Motor Planning, Not Execution, Separates Motor Memories
title_full Motor Planning, Not Execution, Separates Motor Memories
title_fullStr Motor Planning, Not Execution, Separates Motor Memories
title_full_unstemmed Motor Planning, Not Execution, Separates Motor Memories
title_short Motor Planning, Not Execution, Separates Motor Memories
title_sort motor planning, not execution, separates motor memories
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5167294/
https://www.ncbi.nlm.nih.gov/pubmed/27817979
http://dx.doi.org/10.1016/j.neuron.2016.10.017
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