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Beyond reward prediction errors: the role of dopamine in movement kinematics

We recorded activity of dopamine (DA) neurons in the substantia nigra pars compacta in unrestrained mice while monitoring their movements with video tracking. Our approach allows an unbiased examination of the continuous relationship between single unit activity and behavior. Although DA neurons sho...

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Autores principales: Barter, Joseph W., Li, Suellen, Lu, Dongye, Bartholomew, Ryan A., Rossi, Mark A., Shoemaker, Charles T., Salas-Meza, Daniel, Gaidis, Erin, Yin, Henry H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444742/
https://www.ncbi.nlm.nih.gov/pubmed/26074791
http://dx.doi.org/10.3389/fnint.2015.00039
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author Barter, Joseph W.
Li, Suellen
Lu, Dongye
Bartholomew, Ryan A.
Rossi, Mark A.
Shoemaker, Charles T.
Salas-Meza, Daniel
Gaidis, Erin
Yin, Henry H.
author_facet Barter, Joseph W.
Li, Suellen
Lu, Dongye
Bartholomew, Ryan A.
Rossi, Mark A.
Shoemaker, Charles T.
Salas-Meza, Daniel
Gaidis, Erin
Yin, Henry H.
author_sort Barter, Joseph W.
collection PubMed
description We recorded activity of dopamine (DA) neurons in the substantia nigra pars compacta in unrestrained mice while monitoring their movements with video tracking. Our approach allows an unbiased examination of the continuous relationship between single unit activity and behavior. Although DA neurons show characteristic burst firing following cue or reward presentation, as previously reported, their activity can be explained by the representation of actual movement kinematics. Unlike neighboring pars reticulata GABAergic output neurons, which can represent vector components of position, DA neurons represent vector components of velocity or acceleration. We found neurons related to movements in four directions—up, down, left, right. For horizontal movements, there is significant lateralization of neurons: the left nigra contains more rightward neurons, whereas the right nigra contains more leftward neurons. The relationship between DA activity and movement kinematics was found on both appetitive trials using sucrose and aversive trials using air puff, showing that these neurons belong to a velocity control circuit that can be used for any number of purposes, whether to seek reward or to avoid harm. In support of this conclusion, mimicry of the phasic activation of DA neurons with selective optogenetic stimulation could also generate movements. Contrary to the popular hypothesis that DA neurons encode reward prediction errors, our results suggest that nigrostriatal DA plays an essential role in controlling the kinematics of voluntary movements. We hypothesize that DA signaling implements gain adjustment for adaptive transition control, and describe a new model of the basal ganglia (BG) in which DA functions to adjust the gain of the transition controller. This model has significant implications for our understanding of movement disorders implicating DA and the BG.
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spelling pubmed-44447422015-06-12 Beyond reward prediction errors: the role of dopamine in movement kinematics Barter, Joseph W. Li, Suellen Lu, Dongye Bartholomew, Ryan A. Rossi, Mark A. Shoemaker, Charles T. Salas-Meza, Daniel Gaidis, Erin Yin, Henry H. Front Integr Neurosci Neuroscience We recorded activity of dopamine (DA) neurons in the substantia nigra pars compacta in unrestrained mice while monitoring their movements with video tracking. Our approach allows an unbiased examination of the continuous relationship between single unit activity and behavior. Although DA neurons show characteristic burst firing following cue or reward presentation, as previously reported, their activity can be explained by the representation of actual movement kinematics. Unlike neighboring pars reticulata GABAergic output neurons, which can represent vector components of position, DA neurons represent vector components of velocity or acceleration. We found neurons related to movements in four directions—up, down, left, right. For horizontal movements, there is significant lateralization of neurons: the left nigra contains more rightward neurons, whereas the right nigra contains more leftward neurons. The relationship between DA activity and movement kinematics was found on both appetitive trials using sucrose and aversive trials using air puff, showing that these neurons belong to a velocity control circuit that can be used for any number of purposes, whether to seek reward or to avoid harm. In support of this conclusion, mimicry of the phasic activation of DA neurons with selective optogenetic stimulation could also generate movements. Contrary to the popular hypothesis that DA neurons encode reward prediction errors, our results suggest that nigrostriatal DA plays an essential role in controlling the kinematics of voluntary movements. We hypothesize that DA signaling implements gain adjustment for adaptive transition control, and describe a new model of the basal ganglia (BG) in which DA functions to adjust the gain of the transition controller. This model has significant implications for our understanding of movement disorders implicating DA and the BG. Frontiers Media S.A. 2015-05-27 /pmc/articles/PMC4444742/ /pubmed/26074791 http://dx.doi.org/10.3389/fnint.2015.00039 Text en Copyright © 2015 Barter, Li, Lu, Bartholomew, Rossi, Shoemaker, Salas-Meza, Gaidis and Yin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Barter, Joseph W.
Li, Suellen
Lu, Dongye
Bartholomew, Ryan A.
Rossi, Mark A.
Shoemaker, Charles T.
Salas-Meza, Daniel
Gaidis, Erin
Yin, Henry H.
Beyond reward prediction errors: the role of dopamine in movement kinematics
title Beyond reward prediction errors: the role of dopamine in movement kinematics
title_full Beyond reward prediction errors: the role of dopamine in movement kinematics
title_fullStr Beyond reward prediction errors: the role of dopamine in movement kinematics
title_full_unstemmed Beyond reward prediction errors: the role of dopamine in movement kinematics
title_short Beyond reward prediction errors: the role of dopamine in movement kinematics
title_sort beyond reward prediction errors: the role of dopamine in movement kinematics
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444742/
https://www.ncbi.nlm.nih.gov/pubmed/26074791
http://dx.doi.org/10.3389/fnint.2015.00039
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