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A triple distinction of cerebellar function for oculomotor learning and fatigue compensation

The cerebellum implements error-based motor learning via synaptic gain adaptation of an inverse model, i.e. the mapping of a spatial movement goal onto a motor command. Recently, we modeled the motor and perceptual changes during learning of saccadic eye movements, showing that learning is actually...

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Autores principales: Masselink, Jana, Cheviet, Alexis, Froment-Tilikete, Caroline, Pélisson, Denis, Lappe, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456158/
https://www.ncbi.nlm.nih.gov/pubmed/37540726
http://dx.doi.org/10.1371/journal.pcbi.1011322
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author Masselink, Jana
Cheviet, Alexis
Froment-Tilikete, Caroline
Pélisson, Denis
Lappe, Markus
author_facet Masselink, Jana
Cheviet, Alexis
Froment-Tilikete, Caroline
Pélisson, Denis
Lappe, Markus
author_sort Masselink, Jana
collection PubMed
description The cerebellum implements error-based motor learning via synaptic gain adaptation of an inverse model, i.e. the mapping of a spatial movement goal onto a motor command. Recently, we modeled the motor and perceptual changes during learning of saccadic eye movements, showing that learning is actually a threefold process. Besides motor recalibration of (1) the inverse model, learning also comprises perceptual recalibration of (2) the visuospatial target map and (3) of a forward dynamics model that estimates the saccade size from corollary discharge. Yet, the site of perceptual recalibration remains unclear. Here we dissociate cerebellar contributions to the three stages of learning by modeling the learning data of eight cerebellar patients and eight healthy controls. Results showed that cerebellar pathology restrains short-term recalibration of the inverse model while the forward dynamics model is well informed about the reduced saccade change. Adaptation of the visuospatial target map trended in learning direction only in control subjects, yet without reaching significance. Moreover, some patients showed a tendency for uncompensated oculomotor fatigue caused by insufficient upregulation of saccade duration. According to our model, this could induce long-term perceptual compensation, consistent with the overestimation of target eccentricity found in the patients’ baseline data. We conclude that the cerebellum mediates short-term adaptation of the inverse model, especially by control of saccade duration, while the forward dynamics model was not affected by cerebellar pathology.
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spelling pubmed-104561582023-08-26 A triple distinction of cerebellar function for oculomotor learning and fatigue compensation Masselink, Jana Cheviet, Alexis Froment-Tilikete, Caroline Pélisson, Denis Lappe, Markus PLoS Comput Biol Research Article The cerebellum implements error-based motor learning via synaptic gain adaptation of an inverse model, i.e. the mapping of a spatial movement goal onto a motor command. Recently, we modeled the motor and perceptual changes during learning of saccadic eye movements, showing that learning is actually a threefold process. Besides motor recalibration of (1) the inverse model, learning also comprises perceptual recalibration of (2) the visuospatial target map and (3) of a forward dynamics model that estimates the saccade size from corollary discharge. Yet, the site of perceptual recalibration remains unclear. Here we dissociate cerebellar contributions to the three stages of learning by modeling the learning data of eight cerebellar patients and eight healthy controls. Results showed that cerebellar pathology restrains short-term recalibration of the inverse model while the forward dynamics model is well informed about the reduced saccade change. Adaptation of the visuospatial target map trended in learning direction only in control subjects, yet without reaching significance. Moreover, some patients showed a tendency for uncompensated oculomotor fatigue caused by insufficient upregulation of saccade duration. According to our model, this could induce long-term perceptual compensation, consistent with the overestimation of target eccentricity found in the patients’ baseline data. We conclude that the cerebellum mediates short-term adaptation of the inverse model, especially by control of saccade duration, while the forward dynamics model was not affected by cerebellar pathology. Public Library of Science 2023-08-04 /pmc/articles/PMC10456158/ /pubmed/37540726 http://dx.doi.org/10.1371/journal.pcbi.1011322 Text en © 2023 Masselink et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Masselink, Jana
Cheviet, Alexis
Froment-Tilikete, Caroline
Pélisson, Denis
Lappe, Markus
A triple distinction of cerebellar function for oculomotor learning and fatigue compensation
title A triple distinction of cerebellar function for oculomotor learning and fatigue compensation
title_full A triple distinction of cerebellar function for oculomotor learning and fatigue compensation
title_fullStr A triple distinction of cerebellar function for oculomotor learning and fatigue compensation
title_full_unstemmed A triple distinction of cerebellar function for oculomotor learning and fatigue compensation
title_short A triple distinction of cerebellar function for oculomotor learning and fatigue compensation
title_sort triple distinction of cerebellar function for oculomotor learning and fatigue compensation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10456158/
https://www.ncbi.nlm.nih.gov/pubmed/37540726
http://dx.doi.org/10.1371/journal.pcbi.1011322
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