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Expectancy-related changes in firing of dopamine neurons depend on hippocampus
The orbitofrontal cortex (OFC) and hippocampus (HC) are both implicated in forming the cognitive or task maps that support flexible behavior. Previously, we used the dopamine neurons as a sensor or tool to measure the functional effects of OFC lesions (Takahashi et al., 2011). We recorded midbrain d...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541105/ https://www.ncbi.nlm.nih.gov/pubmed/37781610 http://dx.doi.org/10.1101/2023.07.19.549728 |
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author | Takahashi, Yuji K. Zhang, Zhewei Montesinos-Cartegena, Marlian Kahnt, Thorsten Langdon, Angela J. Schoenbaum, Geoffrey |
author_facet | Takahashi, Yuji K. Zhang, Zhewei Montesinos-Cartegena, Marlian Kahnt, Thorsten Langdon, Angela J. Schoenbaum, Geoffrey |
author_sort | Takahashi, Yuji K. |
collection | PubMed |
description | The orbitofrontal cortex (OFC) and hippocampus (HC) are both implicated in forming the cognitive or task maps that support flexible behavior. Previously, we used the dopamine neurons as a sensor or tool to measure the functional effects of OFC lesions (Takahashi et al., 2011). We recorded midbrain dopamine neurons as rats performed an odor-based choice task, in which errors in the prediction of reward were induced by manipulating the number or timing of the expected rewards across blocks of trials. We found that OFC lesions ipsilateral to the recording electrodes caused prediction errors to be degraded consistent with a loss in the resolution of the task states, particularly under conditions where hidden information was critical to sharpening the predictions. Here we have repeated this experiment, along with computational modeling of the results, in rats with ipsilateral HC lesions. The results show HC also shapes the map of our task, however unlike OFC, which provides information local to the trial, the HC appears to be necessary for estimating the upper-level hidden states based on the information that is discontinuous or separated by longer timescales. The results contrast the respective roles of the OFC and HC in cognitive mapping and add to evidence that the dopamine neurons access a rich information set from distributed regions regarding the predictive structure of the environment, potentially enabling this powerful teaching signal to support complex learning and behavior. |
format | Online Article Text |
id | pubmed-10541105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-105411052023-10-01 Expectancy-related changes in firing of dopamine neurons depend on hippocampus Takahashi, Yuji K. Zhang, Zhewei Montesinos-Cartegena, Marlian Kahnt, Thorsten Langdon, Angela J. Schoenbaum, Geoffrey bioRxiv Article The orbitofrontal cortex (OFC) and hippocampus (HC) are both implicated in forming the cognitive or task maps that support flexible behavior. Previously, we used the dopamine neurons as a sensor or tool to measure the functional effects of OFC lesions (Takahashi et al., 2011). We recorded midbrain dopamine neurons as rats performed an odor-based choice task, in which errors in the prediction of reward were induced by manipulating the number or timing of the expected rewards across blocks of trials. We found that OFC lesions ipsilateral to the recording electrodes caused prediction errors to be degraded consistent with a loss in the resolution of the task states, particularly under conditions where hidden information was critical to sharpening the predictions. Here we have repeated this experiment, along with computational modeling of the results, in rats with ipsilateral HC lesions. The results show HC also shapes the map of our task, however unlike OFC, which provides information local to the trial, the HC appears to be necessary for estimating the upper-level hidden states based on the information that is discontinuous or separated by longer timescales. The results contrast the respective roles of the OFC and HC in cognitive mapping and add to evidence that the dopamine neurons access a rich information set from distributed regions regarding the predictive structure of the environment, potentially enabling this powerful teaching signal to support complex learning and behavior. Cold Spring Harbor Laboratory 2023-07-21 /pmc/articles/PMC10541105/ /pubmed/37781610 http://dx.doi.org/10.1101/2023.07.19.549728 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Article Takahashi, Yuji K. Zhang, Zhewei Montesinos-Cartegena, Marlian Kahnt, Thorsten Langdon, Angela J. Schoenbaum, Geoffrey Expectancy-related changes in firing of dopamine neurons depend on hippocampus |
title | Expectancy-related changes in firing of dopamine neurons depend on hippocampus |
title_full | Expectancy-related changes in firing of dopamine neurons depend on hippocampus |
title_fullStr | Expectancy-related changes in firing of dopamine neurons depend on hippocampus |
title_full_unstemmed | Expectancy-related changes in firing of dopamine neurons depend on hippocampus |
title_short | Expectancy-related changes in firing of dopamine neurons depend on hippocampus |
title_sort | expectancy-related changes in firing of dopamine neurons depend on hippocampus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541105/ https://www.ncbi.nlm.nih.gov/pubmed/37781610 http://dx.doi.org/10.1101/2023.07.19.549728 |
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