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Tandem internal models execute motor learning in the cerebellum
In performing skillful movement, humans use predictions from internal models formed by repetition learning. However, the computational organization of internal models in the brain remains unknown. Here, we demonstrate that a computational architecture employing a tandem configuration of forward and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048491/ https://www.ncbi.nlm.nih.gov/pubmed/29941578 http://dx.doi.org/10.1073/pnas.1716489115 |
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author | Honda, Takeru Nagao, Soichi Hashimoto, Yuji Ishikawa, Kinya Yokota, Takanori Mizusawa, Hidehiro Ito, Masao |
author_facet | Honda, Takeru Nagao, Soichi Hashimoto, Yuji Ishikawa, Kinya Yokota, Takanori Mizusawa, Hidehiro Ito, Masao |
author_sort | Honda, Takeru |
collection | PubMed |
description | In performing skillful movement, humans use predictions from internal models formed by repetition learning. However, the computational organization of internal models in the brain remains unknown. Here, we demonstrate that a computational architecture employing a tandem configuration of forward and inverse internal models enables efficient motor learning in the cerebellum. The model predicted learning adaptations observed in hand-reaching experiments in humans wearing a prism lens and explained the kinetic components of these behavioral adaptations. The tandem system also predicted a form of subliminal motor learning that was experimentally validated after training intentional misses of hand targets. Patients with cerebellar degeneration disease showed behavioral impairments consistent with tandemly arranged internal models. These findings validate computational tandemization of internal models in motor control and its potential uses in more complex forms of learning and cognition. |
format | Online Article Text |
id | pubmed-6048491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-60484912018-07-17 Tandem internal models execute motor learning in the cerebellum Honda, Takeru Nagao, Soichi Hashimoto, Yuji Ishikawa, Kinya Yokota, Takanori Mizusawa, Hidehiro Ito, Masao Proc Natl Acad Sci U S A Biological Sciences In performing skillful movement, humans use predictions from internal models formed by repetition learning. However, the computational organization of internal models in the brain remains unknown. Here, we demonstrate that a computational architecture employing a tandem configuration of forward and inverse internal models enables efficient motor learning in the cerebellum. The model predicted learning adaptations observed in hand-reaching experiments in humans wearing a prism lens and explained the kinetic components of these behavioral adaptations. The tandem system also predicted a form of subliminal motor learning that was experimentally validated after training intentional misses of hand targets. Patients with cerebellar degeneration disease showed behavioral impairments consistent with tandemly arranged internal models. These findings validate computational tandemization of internal models in motor control and its potential uses in more complex forms of learning and cognition. National Academy of Sciences 2018-07-10 2018-06-25 /pmc/articles/PMC6048491/ /pubmed/29941578 http://dx.doi.org/10.1073/pnas.1716489115 Text en Copyright © 2018 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Honda, Takeru Nagao, Soichi Hashimoto, Yuji Ishikawa, Kinya Yokota, Takanori Mizusawa, Hidehiro Ito, Masao Tandem internal models execute motor learning in the cerebellum |
title | Tandem internal models execute motor learning in the cerebellum |
title_full | Tandem internal models execute motor learning in the cerebellum |
title_fullStr | Tandem internal models execute motor learning in the cerebellum |
title_full_unstemmed | Tandem internal models execute motor learning in the cerebellum |
title_short | Tandem internal models execute motor learning in the cerebellum |
title_sort | tandem internal models execute motor learning in the cerebellum |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048491/ https://www.ncbi.nlm.nih.gov/pubmed/29941578 http://dx.doi.org/10.1073/pnas.1716489115 |
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