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Velocity storage mechanism drives a cerebellar clock for predictive eye velocity control

Predictive motor control is ubiquitously employed in animal kingdom to achieve rapid and precise motor action. In most vertebrates large, moving visual scenes induce an optokinetic response (OKR) control of eye movements to stabilize vision. In goldfish, the OKR was found to be predictive after a pr...

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Autores principales: Miki, Shuntaro, Urase, Kohei, Baker, Robert, Hirata, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181809/
https://www.ncbi.nlm.nih.gov/pubmed/32332917
http://dx.doi.org/10.1038/s41598-020-63641-0
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author Miki, Shuntaro
Urase, Kohei
Baker, Robert
Hirata, Yutaka
author_facet Miki, Shuntaro
Urase, Kohei
Baker, Robert
Hirata, Yutaka
author_sort Miki, Shuntaro
collection PubMed
description Predictive motor control is ubiquitously employed in animal kingdom to achieve rapid and precise motor action. In most vertebrates large, moving visual scenes induce an optokinetic response (OKR) control of eye movements to stabilize vision. In goldfish, the OKR was found to be predictive after a prolonged exposure to temporally periodic visual motion. A recent study showed the cerebellum necessary to acquire this predictive OKR (pOKR), but it remained unclear as to whether the cerebellum alone was sufficient. Herein we examined different fish species known to share the basic architecture of cerebellar neuronal circuitry for their ability to acquire pOKR. Carps were shown to acquire pOKR like goldfish while zebrafish and medaka did not, demonstrating the cerebellum alone not to be sufficient. Interestingly, those fish that acquired pOKR were found to exhibit long-lasting optokinetic after nystagmus (OKAN) as opposed to those that didn’t. To directly manipulate OKAN vestibular-neurectomy was performed in goldfish that severely shortened OKAN, but pOKR was acquired comparable to normal animals. These results suggest that the neuronal circuitry producing OKAN, known as the velocity storage mechanism (VSM), is required to acquire pOKR irrespective of OKAN duration. Taken together, we conclude that pOKR is acquired through recurrent cerebellum-brainstem parallel loops in which the cerebellum adjusts VSM signal flow and, in turn, receives appropriately timed eye velocity information to clock visual world motion.
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spelling pubmed-71818092020-04-29 Velocity storage mechanism drives a cerebellar clock for predictive eye velocity control Miki, Shuntaro Urase, Kohei Baker, Robert Hirata, Yutaka Sci Rep Article Predictive motor control is ubiquitously employed in animal kingdom to achieve rapid and precise motor action. In most vertebrates large, moving visual scenes induce an optokinetic response (OKR) control of eye movements to stabilize vision. In goldfish, the OKR was found to be predictive after a prolonged exposure to temporally periodic visual motion. A recent study showed the cerebellum necessary to acquire this predictive OKR (pOKR), but it remained unclear as to whether the cerebellum alone was sufficient. Herein we examined different fish species known to share the basic architecture of cerebellar neuronal circuitry for their ability to acquire pOKR. Carps were shown to acquire pOKR like goldfish while zebrafish and medaka did not, demonstrating the cerebellum alone not to be sufficient. Interestingly, those fish that acquired pOKR were found to exhibit long-lasting optokinetic after nystagmus (OKAN) as opposed to those that didn’t. To directly manipulate OKAN vestibular-neurectomy was performed in goldfish that severely shortened OKAN, but pOKR was acquired comparable to normal animals. These results suggest that the neuronal circuitry producing OKAN, known as the velocity storage mechanism (VSM), is required to acquire pOKR irrespective of OKAN duration. Taken together, we conclude that pOKR is acquired through recurrent cerebellum-brainstem parallel loops in which the cerebellum adjusts VSM signal flow and, in turn, receives appropriately timed eye velocity information to clock visual world motion. Nature Publishing Group UK 2020-04-24 /pmc/articles/PMC7181809/ /pubmed/32332917 http://dx.doi.org/10.1038/s41598-020-63641-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Miki, Shuntaro
Urase, Kohei
Baker, Robert
Hirata, Yutaka
Velocity storage mechanism drives a cerebellar clock for predictive eye velocity control
title Velocity storage mechanism drives a cerebellar clock for predictive eye velocity control
title_full Velocity storage mechanism drives a cerebellar clock for predictive eye velocity control
title_fullStr Velocity storage mechanism drives a cerebellar clock for predictive eye velocity control
title_full_unstemmed Velocity storage mechanism drives a cerebellar clock for predictive eye velocity control
title_short Velocity storage mechanism drives a cerebellar clock for predictive eye velocity control
title_sort velocity storage mechanism drives a cerebellar clock for predictive eye velocity control
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181809/
https://www.ncbi.nlm.nih.gov/pubmed/32332917
http://dx.doi.org/10.1038/s41598-020-63641-0
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