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Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning

To adapt to variable environments, humans regulate their behavior by modulating gains in sensory-to-motor processing. In this study, we measured a simple eye movement, the ocular following response (OFR), in monkeys to study the neuronal basis of adaptive motor learning in the visuomotor processing...

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Autores principales: Takemura, Aya, Ofuji, Tomoyo, Miura, Kenichiro, Kawano, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244411/
https://www.ncbi.nlm.nih.gov/pubmed/28102342
http://dx.doi.org/10.1038/srep40939
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author Takemura, Aya
Ofuji, Tomoyo
Miura, Kenichiro
Kawano, Kenji
author_facet Takemura, Aya
Ofuji, Tomoyo
Miura, Kenichiro
Kawano, Kenji
author_sort Takemura, Aya
collection PubMed
description To adapt to variable environments, humans regulate their behavior by modulating gains in sensory-to-motor processing. In this study, we measured a simple eye movement, the ocular following response (OFR), in monkeys to study the neuronal basis of adaptive motor learning in the visuomotor processing stream. The medial superior temporal (MST) area of the cerebral cortex is a critical site for contextual gain modulation of the OFR. However, the role of MST neurons in adaptive gain modulation of the OFR remains unknown. We adopted a velocity step-down sequence paradigm that was designed to promote adaptive gain modulation of the OFR to investigate the role of the dorsal MST (MSTd) in adaptive motor learning. In the initial learning stage, we observed a reduction in the OFR but no significant change in the “open-loop” responses for the majority of the MSTd neurons. However, in the late learning stage, some MSTd neurons exhibited significantly enhanced “closed-loop” responses in association with increases in retinal error velocity. These results indicate that the MSTd area primarily encodes visual motion, suggesting that MSTd neurons function upstream of the motor learning site to provide sensory signals to the downstream structures involved in adaptive motor learning.
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spelling pubmed-52444112017-01-23 Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning Takemura, Aya Ofuji, Tomoyo Miura, Kenichiro Kawano, Kenji Sci Rep Article To adapt to variable environments, humans regulate their behavior by modulating gains in sensory-to-motor processing. In this study, we measured a simple eye movement, the ocular following response (OFR), in monkeys to study the neuronal basis of adaptive motor learning in the visuomotor processing stream. The medial superior temporal (MST) area of the cerebral cortex is a critical site for contextual gain modulation of the OFR. However, the role of MST neurons in adaptive gain modulation of the OFR remains unknown. We adopted a velocity step-down sequence paradigm that was designed to promote adaptive gain modulation of the OFR to investigate the role of the dorsal MST (MSTd) in adaptive motor learning. In the initial learning stage, we observed a reduction in the OFR but no significant change in the “open-loop” responses for the majority of the MSTd neurons. However, in the late learning stage, some MSTd neurons exhibited significantly enhanced “closed-loop” responses in association with increases in retinal error velocity. These results indicate that the MSTd area primarily encodes visual motion, suggesting that MSTd neurons function upstream of the motor learning site to provide sensory signals to the downstream structures involved in adaptive motor learning. Nature Publishing Group 2017-01-19 /pmc/articles/PMC5244411/ /pubmed/28102342 http://dx.doi.org/10.1038/srep40939 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Takemura, Aya
Ofuji, Tomoyo
Miura, Kenichiro
Kawano, Kenji
Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning
title Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning
title_full Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning
title_fullStr Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning
title_full_unstemmed Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning
title_short Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning
title_sort neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244411/
https://www.ncbi.nlm.nih.gov/pubmed/28102342
http://dx.doi.org/10.1038/srep40939
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