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Coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks

The cerebellum is thought to mediate sensorimotor adaptation through the acquisition of internal models of the body-environment interaction. These representations can be of two types, identified as forward and inverse models. The first predicts the sensory consequences of actions, while the second p...

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Autores principales: Passot, Jean-Baptiste, Luque, Niceto R., Arleo, Angelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711060/
https://www.ncbi.nlm.nih.gov/pubmed/23874289
http://dx.doi.org/10.3389/fncom.2013.00095
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author Passot, Jean-Baptiste
Luque, Niceto R.
Arleo, Angelo
author_facet Passot, Jean-Baptiste
Luque, Niceto R.
Arleo, Angelo
author_sort Passot, Jean-Baptiste
collection PubMed
description The cerebellum is thought to mediate sensorimotor adaptation through the acquisition of internal models of the body-environment interaction. These representations can be of two types, identified as forward and inverse models. The first predicts the sensory consequences of actions, while the second provides the correct commands to achieve desired state transitions. In this paper, we propose a composite architecture consisting of multiple cerebellar internal models to account for the adaptation performance of humans during sensorimotor learning. The proposed model takes inspiration from the cerebellar microcomplex circuit, and employs spiking neurons to process information. We investigate the intrinsic properties of the cerebellar circuitry subserving efficient adaptation properties, and we assess the complementary contributions of internal representations by simulating our model in a procedural adaptation task. Our simulation results suggest that the coupling of internal models enhances learning performance significantly (compared with independent forward and inverse models), and it allows for the reproduction of human adaptation capabilities. Furthermore, we provide a computational explanation for the performance improvement observed after one night of sleep in a wide range of sensorimotor tasks. We predict that internal model coupling is a necessary condition for the offline consolidation of procedural memories.
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spelling pubmed-37110602013-07-19 Coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks Passot, Jean-Baptiste Luque, Niceto R. Arleo, Angelo Front Comput Neurosci Neuroscience The cerebellum is thought to mediate sensorimotor adaptation through the acquisition of internal models of the body-environment interaction. These representations can be of two types, identified as forward and inverse models. The first predicts the sensory consequences of actions, while the second provides the correct commands to achieve desired state transitions. In this paper, we propose a composite architecture consisting of multiple cerebellar internal models to account for the adaptation performance of humans during sensorimotor learning. The proposed model takes inspiration from the cerebellar microcomplex circuit, and employs spiking neurons to process information. We investigate the intrinsic properties of the cerebellar circuitry subserving efficient adaptation properties, and we assess the complementary contributions of internal representations by simulating our model in a procedural adaptation task. Our simulation results suggest that the coupling of internal models enhances learning performance significantly (compared with independent forward and inverse models), and it allows for the reproduction of human adaptation capabilities. Furthermore, we provide a computational explanation for the performance improvement observed after one night of sleep in a wide range of sensorimotor tasks. We predict that internal model coupling is a necessary condition for the offline consolidation of procedural memories. Frontiers Media S.A. 2013-07-15 /pmc/articles/PMC3711060/ /pubmed/23874289 http://dx.doi.org/10.3389/fncom.2013.00095 Text en Copyright © 2013 Passot Luque and Arleo. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Passot, Jean-Baptiste
Luque, Niceto R.
Arleo, Angelo
Coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks
title Coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks
title_full Coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks
title_fullStr Coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks
title_full_unstemmed Coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks
title_short Coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks
title_sort coupling internal cerebellar models enhances online adaptation and supports offline consolidation in sensorimotor tasks
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711060/
https://www.ncbi.nlm.nih.gov/pubmed/23874289
http://dx.doi.org/10.3389/fncom.2013.00095
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