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Cerebellar implementation of movement sequences through feedback

Most movements are not unitary, but are comprised of sequences. Although patients with cerebellar pathology display severe deficits in the execution and learning of sequences (Doyon et al., 1997; Shin and Ivry, 2003), most of our understanding of cerebellar mechanisms has come from analyses of singl...

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Autores principales: Khilkevich, Andrei, Zambrano, Juan, Richards, Molly-Marie, Mauk, Michael Dean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107335/
https://www.ncbi.nlm.nih.gov/pubmed/30063004
http://dx.doi.org/10.7554/eLife.37443
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author Khilkevich, Andrei
Zambrano, Juan
Richards, Molly-Marie
Mauk, Michael Dean
author_facet Khilkevich, Andrei
Zambrano, Juan
Richards, Molly-Marie
Mauk, Michael Dean
author_sort Khilkevich, Andrei
collection PubMed
description Most movements are not unitary, but are comprised of sequences. Although patients with cerebellar pathology display severe deficits in the execution and learning of sequences (Doyon et al., 1997; Shin and Ivry, 2003), most of our understanding of cerebellar mechanisms has come from analyses of single component movements. Eyelid conditioning is a cerebellar-mediated behavior that provides the ability to control and restrict inputs to the cerebellum through stimulation of mossy fibers. We utilized this advantage to test directly how the cerebellum can learn a sequence of inter-connected movement components in rabbits. We show that the feedback signals from one component are sufficient to serve as a cue for the next component in the sequence. In vivo recordings from Purkinje cells demonstrated that all components of the sequence were encoded similarly by cerebellar cortex. These results provide a simple yet general framework for how the cerebellum can use simple associate learning processes to chain together a sequence of appropriately timed responses.
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spelling pubmed-61073352018-08-27 Cerebellar implementation of movement sequences through feedback Khilkevich, Andrei Zambrano, Juan Richards, Molly-Marie Mauk, Michael Dean eLife Neuroscience Most movements are not unitary, but are comprised of sequences. Although patients with cerebellar pathology display severe deficits in the execution and learning of sequences (Doyon et al., 1997; Shin and Ivry, 2003), most of our understanding of cerebellar mechanisms has come from analyses of single component movements. Eyelid conditioning is a cerebellar-mediated behavior that provides the ability to control and restrict inputs to the cerebellum through stimulation of mossy fibers. We utilized this advantage to test directly how the cerebellum can learn a sequence of inter-connected movement components in rabbits. We show that the feedback signals from one component are sufficient to serve as a cue for the next component in the sequence. In vivo recordings from Purkinje cells demonstrated that all components of the sequence were encoded similarly by cerebellar cortex. These results provide a simple yet general framework for how the cerebellum can use simple associate learning processes to chain together a sequence of appropriately timed responses. eLife Sciences Publications, Ltd 2018-07-31 /pmc/articles/PMC6107335/ /pubmed/30063004 http://dx.doi.org/10.7554/eLife.37443 Text en © 2018, Khilkevich et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Khilkevich, Andrei
Zambrano, Juan
Richards, Molly-Marie
Mauk, Michael Dean
Cerebellar implementation of movement sequences through feedback
title Cerebellar implementation of movement sequences through feedback
title_full Cerebellar implementation of movement sequences through feedback
title_fullStr Cerebellar implementation of movement sequences through feedback
title_full_unstemmed Cerebellar implementation of movement sequences through feedback
title_short Cerebellar implementation of movement sequences through feedback
title_sort cerebellar implementation of movement sequences through feedback
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107335/
https://www.ncbi.nlm.nih.gov/pubmed/30063004
http://dx.doi.org/10.7554/eLife.37443
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