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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sg-ntu-dr.10356-821542022-02-16T16:29:02Z The cerebellum linearly encodes whisker position during voluntary movement Chen, Susu Augustine, George James Chadderton, Paul Lee Kong Chian School of Medicine (LKCMedicine) whisker system cerebellum 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. NRF (Natl Research Foundation, S’pore) Published version 2016-08-15T08:19:40Z 2019-12-06T14:47:40Z 2016-08-15T08:19:40Z 2019-12-06T14:47:40Z 2015 Journal Article Chen, S., Augustine, G. J., & Chadderton, P. (2016). The cerebellum linearly encodes whisker position during voluntary movement. eLife, 5, e10509-. https://hdl.handle.net/10356/82154 http://hdl.handle.net/10220/41132 10.7554/eLife.10509 26780828 en eLife © 2015, Chen et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited. 16 p. application/pdf |
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whisker system cerebellum Chen, Susu Augustine, George James Chadderton, Paul The cerebellum linearly encodes whisker position during voluntary movement |
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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. |
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Lee Kong Chian School of Medicine (LKCMedicine) |
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Lee Kong Chian School of Medicine (LKCMedicine) Chen, Susu Augustine, George James Chadderton, Paul |
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Article |
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Chen, Susu Augustine, George James Chadderton, Paul |
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Chen, Susu |
title |
The cerebellum linearly encodes whisker position during voluntary movement |
title_short |
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_sort |
cerebellum linearly encodes whisker position during voluntary movement |
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2016 |
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https://hdl.handle.net/10356/82154 http://hdl.handle.net/10220/41132 |
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1725985506237349888 |