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Dopamine subsystems that track internal states

Food and water are rewarding in part because they satisfy our internal needs(1,2). Dopaminergic neurons in the ventral tegmental area (VTA) are activated by gustatory rewards(3–5), but how animals learn to associate these oral cues with the delayed physiological effects of ingestion is unknown. Here...

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Autores principales: Grove, James C. R., Gray, Lindsay A., La Santa Medina, Naymalis, Sivakumar, Nilla, Ahn, Jamie S., Corpuz, Timothy V., Berke, Joshua D., Kreitzer, Anatol C., Knight, Zachary A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365689/
https://www.ncbi.nlm.nih.gov/pubmed/35831501
http://dx.doi.org/10.1038/s41586-022-04954-0
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author Grove, James C. R.
Gray, Lindsay A.
La Santa Medina, Naymalis
Sivakumar, Nilla
Ahn, Jamie S.
Corpuz, Timothy V.
Berke, Joshua D.
Kreitzer, Anatol C.
Knight, Zachary A.
author_facet Grove, James C. R.
Gray, Lindsay A.
La Santa Medina, Naymalis
Sivakumar, Nilla
Ahn, Jamie S.
Corpuz, Timothy V.
Berke, Joshua D.
Kreitzer, Anatol C.
Knight, Zachary A.
author_sort Grove, James C. R.
collection PubMed
description Food and water are rewarding in part because they satisfy our internal needs(1,2). Dopaminergic neurons in the ventral tegmental area (VTA) are activated by gustatory rewards(3–5), but how animals learn to associate these oral cues with the delayed physiological effects of ingestion is unknown. Here we show that individual dopaminergic neurons in the VTA respond to detection of nutrients or water at specific stages of ingestion. A major subset of dopaminergic neurons tracks changes in systemic hydration that occur tens of minutes after thirsty mice drink water, whereas different dopaminergic neurons respond to nutrients in the gastrointestinal tract. We show that information about fluid balance is transmitted to the VTA by a hypothalamic pathway and then re-routed to downstream circuits that track the oral, gastrointestinal and post-absorptive stages of ingestion. To investigate the function of these signals, we used a paradigm in which a fluid’s oral and post-absorptive effects can be independently manipulated and temporally separated. We show that mice rapidly learn to prefer one fluid over another based solely on its rehydrating ability and that this post-ingestive learning is prevented if dopaminergic neurons in the VTA are selectively silenced after consumption. These findings reveal that the midbrain dopamine system contains subsystems that track different modalities and stages of ingestion, on timescales from seconds to tens of minutes, and that this information is used to drive learning about the consequences of ingestion.
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spelling pubmed-93656892022-08-12 Dopamine subsystems that track internal states Grove, James C. R. Gray, Lindsay A. La Santa Medina, Naymalis Sivakumar, Nilla Ahn, Jamie S. Corpuz, Timothy V. Berke, Joshua D. Kreitzer, Anatol C. Knight, Zachary A. Nature Article Food and water are rewarding in part because they satisfy our internal needs(1,2). Dopaminergic neurons in the ventral tegmental area (VTA) are activated by gustatory rewards(3–5), but how animals learn to associate these oral cues with the delayed physiological effects of ingestion is unknown. Here we show that individual dopaminergic neurons in the VTA respond to detection of nutrients or water at specific stages of ingestion. A major subset of dopaminergic neurons tracks changes in systemic hydration that occur tens of minutes after thirsty mice drink water, whereas different dopaminergic neurons respond to nutrients in the gastrointestinal tract. We show that information about fluid balance is transmitted to the VTA by a hypothalamic pathway and then re-routed to downstream circuits that track the oral, gastrointestinal and post-absorptive stages of ingestion. To investigate the function of these signals, we used a paradigm in which a fluid’s oral and post-absorptive effects can be independently manipulated and temporally separated. We show that mice rapidly learn to prefer one fluid over another based solely on its rehydrating ability and that this post-ingestive learning is prevented if dopaminergic neurons in the VTA are selectively silenced after consumption. These findings reveal that the midbrain dopamine system contains subsystems that track different modalities and stages of ingestion, on timescales from seconds to tens of minutes, and that this information is used to drive learning about the consequences of ingestion. Nature Publishing Group UK 2022-07-13 2022 /pmc/articles/PMC9365689/ /pubmed/35831501 http://dx.doi.org/10.1038/s41586-022-04954-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Grove, James C. R.
Gray, Lindsay A.
La Santa Medina, Naymalis
Sivakumar, Nilla
Ahn, Jamie S.
Corpuz, Timothy V.
Berke, Joshua D.
Kreitzer, Anatol C.
Knight, Zachary A.
Dopamine subsystems that track internal states
title Dopamine subsystems that track internal states
title_full Dopamine subsystems that track internal states
title_fullStr Dopamine subsystems that track internal states
title_full_unstemmed Dopamine subsystems that track internal states
title_short Dopamine subsystems that track internal states
title_sort dopamine subsystems that track internal states
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9365689/
https://www.ncbi.nlm.nih.gov/pubmed/35831501
http://dx.doi.org/10.1038/s41586-022-04954-0
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