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Distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks
The cerebellum plays a crucial role in motor learning and it acts as a predictive controller. Modeling it and embedding it into sensorimotor tasks allows us to create functional links between plasticity mechanisms, neural circuits and behavioral learning. Moreover, if applied to real-time control of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340181/ https://www.ncbi.nlm.nih.gov/pubmed/25762922 http://dx.doi.org/10.3389/fncom.2015.00024 |
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author | Casellato, Claudia Antonietti, Alberto Garrido, Jesus A. Ferrigno, Giancarlo D'Angelo, Egidio Pedrocchi, Alessandra |
author_facet | Casellato, Claudia Antonietti, Alberto Garrido, Jesus A. Ferrigno, Giancarlo D'Angelo, Egidio Pedrocchi, Alessandra |
author_sort | Casellato, Claudia |
collection | PubMed |
description | The cerebellum plays a crucial role in motor learning and it acts as a predictive controller. Modeling it and embedding it into sensorimotor tasks allows us to create functional links between plasticity mechanisms, neural circuits and behavioral learning. Moreover, if applied to real-time control of a neurorobot, the cerebellar model has to deal with a real noisy and changing environment, thus showing its robustness and effectiveness in learning. A biologically inspired cerebellar model with distributed plasticity, both at cortical and nuclear sites, has been used. Two cerebellum-mediated paradigms have been designed: an associative Pavlovian task and a vestibulo-ocular reflex, with multiple sessions of acquisition and extinction and with different stimuli and perturbation patterns. The cerebellar controller succeeded to generate conditioned responses and finely tuned eye movement compensation, thus reproducing human-like behaviors. Through a productive plasticity transfer from cortical to nuclear sites, the distributed cerebellar controller showed in both tasks the capability to optimize learning on multiple time-scales, to store motor memory and to effectively adapt to dynamic ranges of stimuli. |
format | Online Article Text |
id | pubmed-4340181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43401812015-03-11 Distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks Casellato, Claudia Antonietti, Alberto Garrido, Jesus A. Ferrigno, Giancarlo D'Angelo, Egidio Pedrocchi, Alessandra Front Comput Neurosci Neuroscience The cerebellum plays a crucial role in motor learning and it acts as a predictive controller. Modeling it and embedding it into sensorimotor tasks allows us to create functional links between plasticity mechanisms, neural circuits and behavioral learning. Moreover, if applied to real-time control of a neurorobot, the cerebellar model has to deal with a real noisy and changing environment, thus showing its robustness and effectiveness in learning. A biologically inspired cerebellar model with distributed plasticity, both at cortical and nuclear sites, has been used. Two cerebellum-mediated paradigms have been designed: an associative Pavlovian task and a vestibulo-ocular reflex, with multiple sessions of acquisition and extinction and with different stimuli and perturbation patterns. The cerebellar controller succeeded to generate conditioned responses and finely tuned eye movement compensation, thus reproducing human-like behaviors. Through a productive plasticity transfer from cortical to nuclear sites, the distributed cerebellar controller showed in both tasks the capability to optimize learning on multiple time-scales, to store motor memory and to effectively adapt to dynamic ranges of stimuli. Frontiers Media S.A. 2015-02-25 /pmc/articles/PMC4340181/ /pubmed/25762922 http://dx.doi.org/10.3389/fncom.2015.00024 Text en Copyright © 2015 Casellato, Antonietti, Garrido, Ferrigno, D'Angelo and Pedrocchi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Casellato, Claudia Antonietti, Alberto Garrido, Jesus A. Ferrigno, Giancarlo D'Angelo, Egidio Pedrocchi, Alessandra Distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks |
title | Distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks |
title_full | Distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks |
title_fullStr | Distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks |
title_full_unstemmed | Distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks |
title_short | Distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks |
title_sort | distributed cerebellar plasticity implements generalized multiple-scale memory components in real-robot sensorimotor tasks |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4340181/ https://www.ncbi.nlm.nih.gov/pubmed/25762922 http://dx.doi.org/10.3389/fncom.2015.00024 |
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