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Dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior
Dopamine release in the nucleus accumbens (NAc) is causally linked to adaptive aversive learning, and its dysregulation is a core phenotype in anxiety and stress disorders. Here, we record NAc core dopamine during a task where mice learn to discriminate between cues signaling two types of outcomes:...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528296/ https://www.ncbi.nlm.nih.gov/pubmed/37543945 http://dx.doi.org/10.1016/j.celrep.2023.112948 |
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author | Kutlu, Munir Gunes Tat, Jennifer Christensen, Brooke A. Zachry, Jennifer E. Calipari, Erin S. |
author_facet | Kutlu, Munir Gunes Tat, Jennifer Christensen, Brooke A. Zachry, Jennifer E. Calipari, Erin S. |
author_sort | Kutlu, Munir Gunes |
collection | PubMed |
description | Dopamine release in the nucleus accumbens (NAc) is causally linked to adaptive aversive learning, and its dysregulation is a core phenotype in anxiety and stress disorders. Here, we record NAc core dopamine during a task where mice learn to discriminate between cues signaling two types of outcomes: (1) footshock presentation and (2) footshock omission. We show that dopamine release is evoked by footshock omission. This dopamine response is largest when the omission is unexpected and decreases over learning, and artificially increasing this signal disrupts discrimination learning. Conversely, optogenetic inhibition of dopamine responses to the footshock itself impairs learning. Finally, theory-driven computational modeling suggests that these effects can be explained by dopamine signaling the perceived saliency of predicted aversive events. Together, we elucidate the role of NAc dopamine in aversive learning and offer potential avenues for understanding the neural mechanisms involved in anxiety and stress disorders. |
format | Online Article Text |
id | pubmed-10528296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-105282962023-09-27 Dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior Kutlu, Munir Gunes Tat, Jennifer Christensen, Brooke A. Zachry, Jennifer E. Calipari, Erin S. Cell Rep Article Dopamine release in the nucleus accumbens (NAc) is causally linked to adaptive aversive learning, and its dysregulation is a core phenotype in anxiety and stress disorders. Here, we record NAc core dopamine during a task where mice learn to discriminate between cues signaling two types of outcomes: (1) footshock presentation and (2) footshock omission. We show that dopamine release is evoked by footshock omission. This dopamine response is largest when the omission is unexpected and decreases over learning, and artificially increasing this signal disrupts discrimination learning. Conversely, optogenetic inhibition of dopamine responses to the footshock itself impairs learning. Finally, theory-driven computational modeling suggests that these effects can be explained by dopamine signaling the perceived saliency of predicted aversive events. Together, we elucidate the role of NAc dopamine in aversive learning and offer potential avenues for understanding the neural mechanisms involved in anxiety and stress disorders. 2023-08-29 2023-08-05 /pmc/articles/PMC10528296/ /pubmed/37543945 http://dx.doi.org/10.1016/j.celrep.2023.112948 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Kutlu, Munir Gunes Tat, Jennifer Christensen, Brooke A. Zachry, Jennifer E. Calipari, Erin S. Dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior |
title | Dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior |
title_full | Dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior |
title_fullStr | Dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior |
title_full_unstemmed | Dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior |
title_short | Dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior |
title_sort | dopamine release at the time of a predicted aversive outcome causally controls the trajectory and expression of conditioned behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10528296/ https://www.ncbi.nlm.nih.gov/pubmed/37543945 http://dx.doi.org/10.1016/j.celrep.2023.112948 |
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