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Reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior

A key function of the nervous system is producing adaptive behavior across changing conditions, like physiological state. Although states like thirst and hunger are known to impact decision-making, the neurobiology of this phenomenon has been studied minimally. Here, we tracked evolving preference f...

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Autores principales: Ottenheimer, David J., Wang, Karen, Tong, Xiao, Fraser, Kurt M., Richard, Jocelyn M., Janak, Patricia H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673692/
https://www.ncbi.nlm.nih.gov/pubmed/33148649
http://dx.doi.org/10.1126/sciadv.abc9321
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author Ottenheimer, David J.
Wang, Karen
Tong, Xiao
Fraser, Kurt M.
Richard, Jocelyn M.
Janak, Patricia H.
author_facet Ottenheimer, David J.
Wang, Karen
Tong, Xiao
Fraser, Kurt M.
Richard, Jocelyn M.
Janak, Patricia H.
author_sort Ottenheimer, David J.
collection PubMed
description A key function of the nervous system is producing adaptive behavior across changing conditions, like physiological state. Although states like thirst and hunger are known to impact decision-making, the neurobiology of this phenomenon has been studied minimally. Here, we tracked evolving preference for sucrose and water as rats proceeded from a thirsty to sated state. As rats shifted from water choices to sucrose choices across the session, the activity of a majority of neurons in the ventral pallidum, a region crucial for reward-related behaviors, closely matched the evolving behavioral preference. The timing of this signal followed the pattern of a reward prediction error, occurring at the cue or the reward depending on when reward identity was revealed. Additionally, optogenetic stimulation of ventral pallidum neurons at the time of reward was able to reverse behavioral preference. Our results suggest that ventral pallidum neurons guide reward-related decisions across changing physiological states.
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spelling pubmed-76736922020-11-24 Reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior Ottenheimer, David J. Wang, Karen Tong, Xiao Fraser, Kurt M. Richard, Jocelyn M. Janak, Patricia H. Sci Adv Research Articles A key function of the nervous system is producing adaptive behavior across changing conditions, like physiological state. Although states like thirst and hunger are known to impact decision-making, the neurobiology of this phenomenon has been studied minimally. Here, we tracked evolving preference for sucrose and water as rats proceeded from a thirsty to sated state. As rats shifted from water choices to sucrose choices across the session, the activity of a majority of neurons in the ventral pallidum, a region crucial for reward-related behaviors, closely matched the evolving behavioral preference. The timing of this signal followed the pattern of a reward prediction error, occurring at the cue or the reward depending on when reward identity was revealed. Additionally, optogenetic stimulation of ventral pallidum neurons at the time of reward was able to reverse behavioral preference. Our results suggest that ventral pallidum neurons guide reward-related decisions across changing physiological states. American Association for the Advancement of Science 2020-11-04 /pmc/articles/PMC7673692/ /pubmed/33148649 http://dx.doi.org/10.1126/sciadv.abc9321 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Ottenheimer, David J.
Wang, Karen
Tong, Xiao
Fraser, Kurt M.
Richard, Jocelyn M.
Janak, Patricia H.
Reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior
title Reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior
title_full Reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior
title_fullStr Reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior
title_full_unstemmed Reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior
title_short Reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior
title_sort reward activity in ventral pallidum tracks satiety-sensitive preference and drives choice behavior
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673692/
https://www.ncbi.nlm.nih.gov/pubmed/33148649
http://dx.doi.org/10.1126/sciadv.abc9321
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