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The Macaque Cerebellar Flocculus Outputs a Forward Model of Eye Movement

The central nervous system (CNS) achieves fine motor control by generating predictions of the consequences of the motor command, often called forward models of the movement. These predictions are used centrally to detect not-self generated sensations, to modify ongoing movements, and to induce motor...

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Autores principales: Kim, Gyutae, Laurens, Jean, Yakusheva, Tatyana A., Blazquez, Pablo M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460257/
https://www.ncbi.nlm.nih.gov/pubmed/31024268
http://dx.doi.org/10.3389/fnint.2019.00012
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author Kim, Gyutae
Laurens, Jean
Yakusheva, Tatyana A.
Blazquez, Pablo M.
author_facet Kim, Gyutae
Laurens, Jean
Yakusheva, Tatyana A.
Blazquez, Pablo M.
author_sort Kim, Gyutae
collection PubMed
description The central nervous system (CNS) achieves fine motor control by generating predictions of the consequences of the motor command, often called forward models of the movement. These predictions are used centrally to detect not-self generated sensations, to modify ongoing movements, and to induce motor learning. However, finding a neuronal correlate of forward models has proven difficult. In the oculomotor system, we can identify neuronal correlates of forward models vs. neuronal correlates of motor commands by examining neuronal responses during smooth pursuit at eccentric eye positions. During pursuit, torsional eye movement information is not present in the motor command, but it is generated by the mechanic of the orbit. Importantly, the directionality and approximate magnitude of torsional eye movement follow the half angle rule. We use this rule to investigate the role of the cerebellar flocculus complex (FL, flocculus and ventral paraflocculus) in the generation of forward models of the eye. We found that mossy fibers (input elements to the FL) did not change their response to pursuit with eccentricity. Thus, they do not carry torsional eye movement information. However, vertical Purkinje cells (PCs; output elements of the FL) showed a preference for counter-clockwise (CCW) eye velocity [corresponding to extorsion (outward rotation) of the ipsilateral eye]. We hypothesize that FL computes an estimate of torsional eye movement since torsion is present in PCs but not in mossy fibers. Overall, our results add to those of other laboratories in supporting the existence in the CNS of a predictive signal constructed from motor command information.
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spelling pubmed-64602572019-04-25 The Macaque Cerebellar Flocculus Outputs a Forward Model of Eye Movement Kim, Gyutae Laurens, Jean Yakusheva, Tatyana A. Blazquez, Pablo M. Front Integr Neurosci Neuroscience The central nervous system (CNS) achieves fine motor control by generating predictions of the consequences of the motor command, often called forward models of the movement. These predictions are used centrally to detect not-self generated sensations, to modify ongoing movements, and to induce motor learning. However, finding a neuronal correlate of forward models has proven difficult. In the oculomotor system, we can identify neuronal correlates of forward models vs. neuronal correlates of motor commands by examining neuronal responses during smooth pursuit at eccentric eye positions. During pursuit, torsional eye movement information is not present in the motor command, but it is generated by the mechanic of the orbit. Importantly, the directionality and approximate magnitude of torsional eye movement follow the half angle rule. We use this rule to investigate the role of the cerebellar flocculus complex (FL, flocculus and ventral paraflocculus) in the generation of forward models of the eye. We found that mossy fibers (input elements to the FL) did not change their response to pursuit with eccentricity. Thus, they do not carry torsional eye movement information. However, vertical Purkinje cells (PCs; output elements of the FL) showed a preference for counter-clockwise (CCW) eye velocity [corresponding to extorsion (outward rotation) of the ipsilateral eye]. We hypothesize that FL computes an estimate of torsional eye movement since torsion is present in PCs but not in mossy fibers. Overall, our results add to those of other laboratories in supporting the existence in the CNS of a predictive signal constructed from motor command information. Frontiers Media S.A. 2019-04-05 /pmc/articles/PMC6460257/ /pubmed/31024268 http://dx.doi.org/10.3389/fnint.2019.00012 Text en Copyright © 2019 Kim, Laurens, Yakusheva and Blazquez. 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) and the copyright owner(s) 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
Kim, Gyutae
Laurens, Jean
Yakusheva, Tatyana A.
Blazquez, Pablo M.
The Macaque Cerebellar Flocculus Outputs a Forward Model of Eye Movement
title The Macaque Cerebellar Flocculus Outputs a Forward Model of Eye Movement
title_full The Macaque Cerebellar Flocculus Outputs a Forward Model of Eye Movement
title_fullStr The Macaque Cerebellar Flocculus Outputs a Forward Model of Eye Movement
title_full_unstemmed The Macaque Cerebellar Flocculus Outputs a Forward Model of Eye Movement
title_short The Macaque Cerebellar Flocculus Outputs a Forward Model of Eye Movement
title_sort macaque cerebellar flocculus outputs a forward model of eye movement
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6460257/
https://www.ncbi.nlm.nih.gov/pubmed/31024268
http://dx.doi.org/10.3389/fnint.2019.00012
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