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Self-configuring feedback loops for sensorimotor control

How dynamic interactions between nervous system regions in mammals performs online motor control remains an unsolved problem. In this paper, we show that feedback control is a simple, yet powerful way to understand the neural dynamics of sensorimotor control. We make our case using a minimal model c...

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Detalles Bibliográficos
Autores principales: Verduzco-Flores, Sergio Oscar, De Schutter, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699696/
https://www.ncbi.nlm.nih.gov/pubmed/36373657
http://dx.doi.org/10.7554/eLife.77216
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author Verduzco-Flores, Sergio Oscar
De Schutter, Erik
author_facet Verduzco-Flores, Sergio Oscar
De Schutter, Erik
author_sort Verduzco-Flores, Sergio Oscar
collection PubMed
description How dynamic interactions between nervous system regions in mammals performs online motor control remains an unsolved problem. In this paper, we show that feedback control is a simple, yet powerful way to understand the neural dynamics of sensorimotor control. We make our case using a minimal model comprising spinal cord, sensory and motor cortex, coupled by long connections that are plastic. It succeeds in learning how to perform reaching movements of a planar arm with 6 muscles in several directions from scratch. The model satisfies biological plausibility constraints, like neural implementation, transmission delays, local synaptic learning and continuous online learning. Using differential Hebbian plasticity the model can go from motor babbling to reaching arbitrary targets in less than 10 min of in silico time. Moreover, independently of the learning mechanism, properly configured feedback control has many emergent properties: neural populations in motor cortex show directional tuning and oscillatory dynamics, the spinal cord creates convergent force fields that add linearly, and movements are ataxic (as in a motor system without a cerebellum).
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spelling pubmed-96996962022-11-26 Self-configuring feedback loops for sensorimotor control Verduzco-Flores, Sergio Oscar De Schutter, Erik eLife Computational and Systems Biology How dynamic interactions between nervous system regions in mammals performs online motor control remains an unsolved problem. In this paper, we show that feedback control is a simple, yet powerful way to understand the neural dynamics of sensorimotor control. We make our case using a minimal model comprising spinal cord, sensory and motor cortex, coupled by long connections that are plastic. It succeeds in learning how to perform reaching movements of a planar arm with 6 muscles in several directions from scratch. The model satisfies biological plausibility constraints, like neural implementation, transmission delays, local synaptic learning and continuous online learning. Using differential Hebbian plasticity the model can go from motor babbling to reaching arbitrary targets in less than 10 min of in silico time. Moreover, independently of the learning mechanism, properly configured feedback control has many emergent properties: neural populations in motor cortex show directional tuning and oscillatory dynamics, the spinal cord creates convergent force fields that add linearly, and movements are ataxic (as in a motor system without a cerebellum). eLife Sciences Publications, Ltd 2022-11-14 /pmc/articles/PMC9699696/ /pubmed/36373657 http://dx.doi.org/10.7554/eLife.77216 Text en © 2022, Verduzco-Flores and De Schutter https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Verduzco-Flores, Sergio Oscar
De Schutter, Erik
Self-configuring feedback loops for sensorimotor control
title Self-configuring feedback loops for sensorimotor control
title_full Self-configuring feedback loops for sensorimotor control
title_fullStr Self-configuring feedback loops for sensorimotor control
title_full_unstemmed Self-configuring feedback loops for sensorimotor control
title_short Self-configuring feedback loops for sensorimotor control
title_sort self-configuring feedback loops for sensorimotor control
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9699696/
https://www.ncbi.nlm.nih.gov/pubmed/36373657
http://dx.doi.org/10.7554/eLife.77216
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