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Reward expectation extinction restructures and degrades CA1 spatial maps through loss of a dopaminergic reward proximity signal
Hippocampal place cells support reward-related spatial memories by forming a cognitive map that over-represents reward locations. The strength of these memories is modulated by the extent of reward expectation during encoding. However, the circuit mechanisms underlying this modulation are unclear. H...
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/PMC9636178/ https://www.ncbi.nlm.nih.gov/pubmed/36333323 http://dx.doi.org/10.1038/s41467-022-34465-5 |
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author | Krishnan, Seetha Heer, Chad Cherian, Chery Sheffield, Mark E. J. |
author_facet | Krishnan, Seetha Heer, Chad Cherian, Chery Sheffield, Mark E. J. |
author_sort | Krishnan, Seetha |
collection | PubMed |
description | Hippocampal place cells support reward-related spatial memories by forming a cognitive map that over-represents reward locations. The strength of these memories is modulated by the extent of reward expectation during encoding. However, the circuit mechanisms underlying this modulation are unclear. Here we find that when reward expectation is extinguished in mice, they remain engaged with their environment, yet place cell over-representation of rewards vanishes, place field remapping throughout the environment increases, and place field trial-to-trial reliability decreases. Interestingly, Ventral Tegmental Area (VTA) dopaminergic axons in CA1 exhibit a ramping reward-proximity signal that depends on reward expectation and inhibiting VTA dopaminergic neurons largely replicates the effects of extinguishing reward expectation. We conclude that changing reward expectation restructures CA1 cognitive maps and determines map reliability by modulating the dopaminergic VTA-CA1 reward-proximity signal. Thus, internal states of high reward expectation enhance encoding of spatial memories by reinforcing hippocampal cognitive maps associated with reward. |
format | Online Article Text |
id | pubmed-9636178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96361782022-11-06 Reward expectation extinction restructures and degrades CA1 spatial maps through loss of a dopaminergic reward proximity signal Krishnan, Seetha Heer, Chad Cherian, Chery Sheffield, Mark E. J. Nat Commun Article Hippocampal place cells support reward-related spatial memories by forming a cognitive map that over-represents reward locations. The strength of these memories is modulated by the extent of reward expectation during encoding. However, the circuit mechanisms underlying this modulation are unclear. Here we find that when reward expectation is extinguished in mice, they remain engaged with their environment, yet place cell over-representation of rewards vanishes, place field remapping throughout the environment increases, and place field trial-to-trial reliability decreases. Interestingly, Ventral Tegmental Area (VTA) dopaminergic axons in CA1 exhibit a ramping reward-proximity signal that depends on reward expectation and inhibiting VTA dopaminergic neurons largely replicates the effects of extinguishing reward expectation. We conclude that changing reward expectation restructures CA1 cognitive maps and determines map reliability by modulating the dopaminergic VTA-CA1 reward-proximity signal. Thus, internal states of high reward expectation enhance encoding of spatial memories by reinforcing hippocampal cognitive maps associated with reward. Nature Publishing Group UK 2022-11-04 /pmc/articles/PMC9636178/ /pubmed/36333323 http://dx.doi.org/10.1038/s41467-022-34465-5 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 Krishnan, Seetha Heer, Chad Cherian, Chery Sheffield, Mark E. J. Reward expectation extinction restructures and degrades CA1 spatial maps through loss of a dopaminergic reward proximity signal |
title | Reward expectation extinction restructures and degrades CA1 spatial maps through loss of a dopaminergic reward proximity signal |
title_full | Reward expectation extinction restructures and degrades CA1 spatial maps through loss of a dopaminergic reward proximity signal |
title_fullStr | Reward expectation extinction restructures and degrades CA1 spatial maps through loss of a dopaminergic reward proximity signal |
title_full_unstemmed | Reward expectation extinction restructures and degrades CA1 spatial maps through loss of a dopaminergic reward proximity signal |
title_short | Reward expectation extinction restructures and degrades CA1 spatial maps through loss of a dopaminergic reward proximity signal |
title_sort | reward expectation extinction restructures and degrades ca1 spatial maps through loss of a dopaminergic reward proximity signal |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636178/ https://www.ncbi.nlm.nih.gov/pubmed/36333323 http://dx.doi.org/10.1038/s41467-022-34465-5 |
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