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The cerebellum linearly encodes whisker position during voluntary movement

Active whisking is an important model sensorimotor behavior, but the function of the cerebellum in the rodent whisker system is unknown. We have made patch clamp recordings from Purkinje cells in vivo to identify whether cerebellar output encodes kinematic features of whisking including the phase an...

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Detalles Bibliográficos
Autores principales: Chen, Susu, Augustine, George J, Chadderton, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737656/
https://www.ncbi.nlm.nih.gov/pubmed/26780828
http://dx.doi.org/10.7554/eLife.10509
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author Chen, Susu
Augustine, George J
Chadderton, Paul
author_facet Chen, Susu
Augustine, George J
Chadderton, Paul
author_sort Chen, Susu
collection PubMed
description Active whisking is an important model sensorimotor behavior, but the function of the cerebellum in the rodent whisker system is unknown. We have made patch clamp recordings from Purkinje cells in vivo to identify whether cerebellar output encodes kinematic features of whisking including the phase and set point. We show that Purkinje cell spiking activity changes strongly during whisking bouts. On average, the changes in simple spike rate coincide with or slightly precede movement, indicating that the synaptic drive responsible for these changes is predominantly of efferent (motor) rather than re-afferent (sensory) origin. Remarkably, on-going changes in simple spike rate provide an accurate linear read-out of whisker set point. Thus, despite receiving several hundred thousand discrete synaptic inputs across a non-linear dendritic tree, Purkinje cells integrate parallel fiber input to generate precise information about whisking kinematics through linear changes in firing rate. DOI: http://dx.doi.org/10.7554/eLife.10509.001
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spelling pubmed-47376562016-02-04 The cerebellum linearly encodes whisker position during voluntary movement Chen, Susu Augustine, George J Chadderton, Paul eLife Neuroscience Active whisking is an important model sensorimotor behavior, but the function of the cerebellum in the rodent whisker system is unknown. We have made patch clamp recordings from Purkinje cells in vivo to identify whether cerebellar output encodes kinematic features of whisking including the phase and set point. We show that Purkinje cell spiking activity changes strongly during whisking bouts. On average, the changes in simple spike rate coincide with or slightly precede movement, indicating that the synaptic drive responsible for these changes is predominantly of efferent (motor) rather than re-afferent (sensory) origin. Remarkably, on-going changes in simple spike rate provide an accurate linear read-out of whisker set point. Thus, despite receiving several hundred thousand discrete synaptic inputs across a non-linear dendritic tree, Purkinje cells integrate parallel fiber input to generate precise information about whisking kinematics through linear changes in firing rate. DOI: http://dx.doi.org/10.7554/eLife.10509.001 eLife Sciences Publications, Ltd 2016-01-19 /pmc/articles/PMC4737656/ /pubmed/26780828 http://dx.doi.org/10.7554/eLife.10509 Text en © 2015, Chen et al 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
Chen, Susu
Augustine, George J
Chadderton, Paul
The cerebellum linearly encodes whisker position during voluntary movement
title The cerebellum linearly encodes whisker position during voluntary movement
title_full The cerebellum linearly encodes whisker position during voluntary movement
title_fullStr The cerebellum linearly encodes whisker position during voluntary movement
title_full_unstemmed The cerebellum linearly encodes whisker position during voluntary movement
title_short The cerebellum linearly encodes whisker position during voluntary movement
title_sort cerebellum linearly encodes whisker position during voluntary movement
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737656/
https://www.ncbi.nlm.nih.gov/pubmed/26780828
http://dx.doi.org/10.7554/eLife.10509
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