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Dopamine in the dorsal bed nucleus of stria terminalis signals Pavlovian sign-tracking and reward violations
Midbrain and striatal dopamine signals have been extremely well characterized over the past several decades, yet novel dopamine signals and functions in reward learning and motivation continue to emerge. A similar characterization of real-time sub-second dopamine signals in areas outside of the stri...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219648/ https://www.ncbi.nlm.nih.gov/pubmed/37232554 http://dx.doi.org/10.7554/eLife.81980 |
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author | Gyawali, Utsav Martin, David A Sun, Fangmiao Li, Yulong Calu, Donna |
author_facet | Gyawali, Utsav Martin, David A Sun, Fangmiao Li, Yulong Calu, Donna |
author_sort | Gyawali, Utsav |
collection | PubMed |
description | Midbrain and striatal dopamine signals have been extremely well characterized over the past several decades, yet novel dopamine signals and functions in reward learning and motivation continue to emerge. A similar characterization of real-time sub-second dopamine signals in areas outside of the striatum has been limited. Recent advances in fluorescent sensor technology and fiber photometry permit the measurement of dopamine binding correlates, which can divulge basic functions of dopamine signaling in non-striatal dopamine terminal regions, like the dorsal bed nucleus of the stria terminalis (dBNST). Here, we record GRAB(DA) signals in the dBNST during a Pavlovian lever autoshaping task. We observe greater Pavlovian cue-evoked dBNST GRAB(DA) signals in sign-tracking (ST) compared to goal-tracking/intermediate (GT/INT) rats and the magnitude of cue-evoked dBNST GRAB(DA) signals decreases immediately following reinforcer-specific satiety. When we deliver unexpected rewards or omit expected rewards, we find that dBNST dopamine signals encode bidirectional reward prediction errors in GT/INT rats, but only positive prediction errors in ST rats. Since sign- and goal-tracking approach strategies are associated with distinct drug relapse vulnerabilities, we examined the effects of experimenter-administered fentanyl on dBNST dopamine associative encoding. Systemic fentanyl injections do not disrupt cue discrimination but generally potentiate dBNST dopamine signals. These results reveal multiple dBNST dopamine correlates of learning and motivation that depend on the Pavlovian approach strategy employed. |
format | Online Article Text |
id | pubmed-10219648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-102196482023-05-27 Dopamine in the dorsal bed nucleus of stria terminalis signals Pavlovian sign-tracking and reward violations Gyawali, Utsav Martin, David A Sun, Fangmiao Li, Yulong Calu, Donna eLife Neuroscience Midbrain and striatal dopamine signals have been extremely well characterized over the past several decades, yet novel dopamine signals and functions in reward learning and motivation continue to emerge. A similar characterization of real-time sub-second dopamine signals in areas outside of the striatum has been limited. Recent advances in fluorescent sensor technology and fiber photometry permit the measurement of dopamine binding correlates, which can divulge basic functions of dopamine signaling in non-striatal dopamine terminal regions, like the dorsal bed nucleus of the stria terminalis (dBNST). Here, we record GRAB(DA) signals in the dBNST during a Pavlovian lever autoshaping task. We observe greater Pavlovian cue-evoked dBNST GRAB(DA) signals in sign-tracking (ST) compared to goal-tracking/intermediate (GT/INT) rats and the magnitude of cue-evoked dBNST GRAB(DA) signals decreases immediately following reinforcer-specific satiety. When we deliver unexpected rewards or omit expected rewards, we find that dBNST dopamine signals encode bidirectional reward prediction errors in GT/INT rats, but only positive prediction errors in ST rats. Since sign- and goal-tracking approach strategies are associated with distinct drug relapse vulnerabilities, we examined the effects of experimenter-administered fentanyl on dBNST dopamine associative encoding. Systemic fentanyl injections do not disrupt cue discrimination but generally potentiate dBNST dopamine signals. These results reveal multiple dBNST dopamine correlates of learning and motivation that depend on the Pavlovian approach strategy employed. eLife Sciences Publications, Ltd 2023-05-26 /pmc/articles/PMC10219648/ /pubmed/37232554 http://dx.doi.org/10.7554/eLife.81980 Text en © 2023, Gyawali et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Gyawali, Utsav Martin, David A Sun, Fangmiao Li, Yulong Calu, Donna Dopamine in the dorsal bed nucleus of stria terminalis signals Pavlovian sign-tracking and reward violations |
title | Dopamine in the dorsal bed nucleus of stria terminalis signals Pavlovian sign-tracking and reward violations |
title_full | Dopamine in the dorsal bed nucleus of stria terminalis signals Pavlovian sign-tracking and reward violations |
title_fullStr | Dopamine in the dorsal bed nucleus of stria terminalis signals Pavlovian sign-tracking and reward violations |
title_full_unstemmed | Dopamine in the dorsal bed nucleus of stria terminalis signals Pavlovian sign-tracking and reward violations |
title_short | Dopamine in the dorsal bed nucleus of stria terminalis signals Pavlovian sign-tracking and reward violations |
title_sort | dopamine in the dorsal bed nucleus of stria terminalis signals pavlovian sign-tracking and reward violations |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10219648/ https://www.ncbi.nlm.nih.gov/pubmed/37232554 http://dx.doi.org/10.7554/eLife.81980 |
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