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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:...

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Detalles Bibliográficos
Autores principales: Kutlu, Munir Gunes, Tat, Jennifer, Christensen, Brooke A., Zachry, Jennifer E., Calipari, Erin S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
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.
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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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