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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9365689 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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