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Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward

Dopamine signaling from the ventral tegmental area (VTA) plays critical roles in reward-related behaviors, but less is known about the functions of neighboring VTA GABAergic neurons. We show here that a primary target of VTA GABA projection neurons is the ventral pallidum (VP). Activity of VTA-to-VP...

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Autores principales: Zhou, Wen-Liang, Kim, Kristen, Ali, Farhan, Pittenger, Steven T., Calarco, Cali A., Mineur, Yann S., Ramakrishnan, Charu, Deisseroth, Karl, Kwan, Alex C., Picciotto, Marina R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581470/
https://www.ncbi.nlm.nih.gov/pubmed/36260661
http://dx.doi.org/10.1126/sciadv.abm5217
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author Zhou, Wen-Liang
Kim, Kristen
Ali, Farhan
Pittenger, Steven T.
Calarco, Cali A.
Mineur, Yann S.
Ramakrishnan, Charu
Deisseroth, Karl
Kwan, Alex C.
Picciotto, Marina R.
author_facet Zhou, Wen-Liang
Kim, Kristen
Ali, Farhan
Pittenger, Steven T.
Calarco, Cali A.
Mineur, Yann S.
Ramakrishnan, Charu
Deisseroth, Karl
Kwan, Alex C.
Picciotto, Marina R.
author_sort Zhou, Wen-Liang
collection PubMed
description Dopamine signaling from the ventral tegmental area (VTA) plays critical roles in reward-related behaviors, but less is known about the functions of neighboring VTA GABAergic neurons. We show here that a primary target of VTA GABA projection neurons is the ventral pallidum (VP). Activity of VTA-to-VP–projecting GABA neurons correlates consistently with size and palatability of the reward and does not change following cue learning, providing a direct measure of reward value. Chemogenetic stimulation of this GABA projection increased activity of a subset of VP neurons that were active while mice were seeking reward. Optogenetic stimulation of this pathway improved performance in a cue-reward task and maintained motivation to work for reward over days. This VTA GABA projection provides information about reward value directly to the VP, likely distinct from the prediction error signal carried by VTA dopamine neurons.
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spelling pubmed-95814702022-10-26 Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward Zhou, Wen-Liang Kim, Kristen Ali, Farhan Pittenger, Steven T. Calarco, Cali A. Mineur, Yann S. Ramakrishnan, Charu Deisseroth, Karl Kwan, Alex C. Picciotto, Marina R. Sci Adv Neuroscience Dopamine signaling from the ventral tegmental area (VTA) plays critical roles in reward-related behaviors, but less is known about the functions of neighboring VTA GABAergic neurons. We show here that a primary target of VTA GABA projection neurons is the ventral pallidum (VP). Activity of VTA-to-VP–projecting GABA neurons correlates consistently with size and palatability of the reward and does not change following cue learning, providing a direct measure of reward value. Chemogenetic stimulation of this GABA projection increased activity of a subset of VP neurons that were active while mice were seeking reward. Optogenetic stimulation of this pathway improved performance in a cue-reward task and maintained motivation to work for reward over days. This VTA GABA projection provides information about reward value directly to the VP, likely distinct from the prediction error signal carried by VTA dopamine neurons. American Association for the Advancement of Science 2022-10-19 /pmc/articles/PMC9581470/ /pubmed/36260661 http://dx.doi.org/10.1126/sciadv.abm5217 Text en Copyright © 2022 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 NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Neuroscience
Zhou, Wen-Liang
Kim, Kristen
Ali, Farhan
Pittenger, Steven T.
Calarco, Cali A.
Mineur, Yann S.
Ramakrishnan, Charu
Deisseroth, Karl
Kwan, Alex C.
Picciotto, Marina R.
Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward
title Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward
title_full Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward
title_fullStr Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward
title_full_unstemmed Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward
title_short Activity of a direct VTA to ventral pallidum GABA pathway encodes unconditioned reward value and sustains motivation for reward
title_sort activity of a direct vta to ventral pallidum gaba pathway encodes unconditioned reward value and sustains motivation for reward
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581470/
https://www.ncbi.nlm.nih.gov/pubmed/36260661
http://dx.doi.org/10.1126/sciadv.abm5217
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