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Mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction
KEY POINTS: Directionality, inherent to movements, has behavioural and neuronal correlates. Direction of vestibular stimulation determines motor learning efficiency. Vestibulo‐ocular reflex gain–increase correlates with Purkinje cell simple spike potentiation. The locus of neural correlates for vest...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538199/ https://www.ncbi.nlm.nih.gov/pubmed/28586131 http://dx.doi.org/10.1113/JP274346 |
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author | Voges, Kai Wu, Bin Post, Laura Schonewille, Martijn De Zeeuw, Chris I. |
author_facet | Voges, Kai Wu, Bin Post, Laura Schonewille, Martijn De Zeeuw, Chris I. |
author_sort | Voges, Kai |
collection | PubMed |
description | KEY POINTS: Directionality, inherent to movements, has behavioural and neuronal correlates. Direction of vestibular stimulation determines motor learning efficiency. Vestibulo‐ocular reflex gain–increase correlates with Purkinje cell simple spike potentiation. The locus of neural correlates for vestibulo‐ocular reflex adaptation is paradigm specific. ABSTRACT: Compensatory eye movements elicited by head rotation, also known as vestibulo‐ocular reflex (VOR), can be adapted with the use of visual feedback. The cerebellum is essential for this type of movement adaptation, although its neuronal correlates remain to be clarified. In the present study, we show that the direction of vestibular input determines the magnitude of eye movement adaptation induced by mismatched visual input in mice, with larger changes during contraversive head rotation. Moreover, the location of the neural correlate of this changed behaviour depends on the type of paradigm. Gain–increase paradigms induce increased simple spike (SS) activity in ipsilateral cerebellar Purkinje cells (PC), which is in line with eye movements triggered by optogenetic PC activation. By contrast, gain–decrease paradigms do not induce changes in SS activity, indicating that the murine vestibulo‐cerebellar cortical circuitry is optimally designed to enhance ipsiversive eye movements. |
format | Online Article Text |
id | pubmed-5538199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55381992017-08-04 Mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction Voges, Kai Wu, Bin Post, Laura Schonewille, Martijn De Zeeuw, Chris I. J Physiol Neuroscience ‐ Behavioural/Systems/Cognitive KEY POINTS: Directionality, inherent to movements, has behavioural and neuronal correlates. Direction of vestibular stimulation determines motor learning efficiency. Vestibulo‐ocular reflex gain–increase correlates with Purkinje cell simple spike potentiation. The locus of neural correlates for vestibulo‐ocular reflex adaptation is paradigm specific. ABSTRACT: Compensatory eye movements elicited by head rotation, also known as vestibulo‐ocular reflex (VOR), can be adapted with the use of visual feedback. The cerebellum is essential for this type of movement adaptation, although its neuronal correlates remain to be clarified. In the present study, we show that the direction of vestibular input determines the magnitude of eye movement adaptation induced by mismatched visual input in mice, with larger changes during contraversive head rotation. Moreover, the location of the neural correlate of this changed behaviour depends on the type of paradigm. Gain–increase paradigms induce increased simple spike (SS) activity in ipsilateral cerebellar Purkinje cells (PC), which is in line with eye movements triggered by optogenetic PC activation. By contrast, gain–decrease paradigms do not induce changes in SS activity, indicating that the murine vestibulo‐cerebellar cortical circuitry is optimally designed to enhance ipsiversive eye movements. John Wiley and Sons Inc. 2017-07-10 2017-08-01 /pmc/articles/PMC5538199/ /pubmed/28586131 http://dx.doi.org/10.1113/JP274346 Text en © 2017 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience ‐ Behavioural/Systems/Cognitive Voges, Kai Wu, Bin Post, Laura Schonewille, Martijn De Zeeuw, Chris I. Mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction |
title | Mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction |
title_full | Mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction |
title_fullStr | Mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction |
title_full_unstemmed | Mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction |
title_short | Mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction |
title_sort | mechanisms underlying vestibulo‐cerebellar motor learning in mice depend on movement direction |
topic | Neuroscience ‐ Behavioural/Systems/Cognitive |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538199/ https://www.ncbi.nlm.nih.gov/pubmed/28586131 http://dx.doi.org/10.1113/JP274346 |
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