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Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction
Fear extinction does not prevent post-traumatic stress or have long-term therapeutic benefits in fear-related disorders unless extinction memories are easily retrieved at later encounters with the once-threatening stimulus. Previous research in rodents has pointed towards a role for spontaneous pref...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191435/ https://www.ncbi.nlm.nih.gov/pubmed/30327462 http://dx.doi.org/10.1038/s41467-018-06785-y |
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author | Gerlicher, A. M. V. Tüscher, O. Kalisch, R. |
author_facet | Gerlicher, A. M. V. Tüscher, O. Kalisch, R. |
author_sort | Gerlicher, A. M. V. |
collection | PubMed |
description | Fear extinction does not prevent post-traumatic stress or have long-term therapeutic benefits in fear-related disorders unless extinction memories are easily retrieved at later encounters with the once-threatening stimulus. Previous research in rodents has pointed towards a role for spontaneous prefrontal activity occurring after extinction learning in stabilizing and consolidating extinction memories. In other memory domains spontaneous post-learning activity has been linked to dopamine. Here, we show that a neural activation pattern — evoked in the ventromedial prefrontal cortex (vmPFC) by the unexpected omission of the feared outcome during extinction learning — spontaneously reappears during postextinction rest. The number of spontaneous vmPFC pattern reactivations predicts extinction memory retrieval and vmPFC activation at test 24 h later. Critically, pharmacologically enhancing dopaminergic activity during extinction consolidation amplifies spontaneous vmPFC reactivations and correspondingly improves extinction memory retrieval at test. Hence, a spontaneous dopamine-dependent memory consolidation-based mechanism may underlie the long-term behavioral effects of fear extinction. |
format | Online Article Text |
id | pubmed-6191435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61914352018-10-19 Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction Gerlicher, A. M. V. Tüscher, O. Kalisch, R. Nat Commun Article Fear extinction does not prevent post-traumatic stress or have long-term therapeutic benefits in fear-related disorders unless extinction memories are easily retrieved at later encounters with the once-threatening stimulus. Previous research in rodents has pointed towards a role for spontaneous prefrontal activity occurring after extinction learning in stabilizing and consolidating extinction memories. In other memory domains spontaneous post-learning activity has been linked to dopamine. Here, we show that a neural activation pattern — evoked in the ventromedial prefrontal cortex (vmPFC) by the unexpected omission of the feared outcome during extinction learning — spontaneously reappears during postextinction rest. The number of spontaneous vmPFC pattern reactivations predicts extinction memory retrieval and vmPFC activation at test 24 h later. Critically, pharmacologically enhancing dopaminergic activity during extinction consolidation amplifies spontaneous vmPFC reactivations and correspondingly improves extinction memory retrieval at test. Hence, a spontaneous dopamine-dependent memory consolidation-based mechanism may underlie the long-term behavioral effects of fear extinction. Nature Publishing Group UK 2018-10-16 /pmc/articles/PMC6191435/ /pubmed/30327462 http://dx.doi.org/10.1038/s41467-018-06785-y Text en © The Author(s) 2018 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/. |
spellingShingle | Article Gerlicher, A. M. V. Tüscher, O. Kalisch, R. Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction |
title | Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction |
title_full | Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction |
title_fullStr | Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction |
title_full_unstemmed | Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction |
title_short | Dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction |
title_sort | dopamine-dependent prefrontal reactivations explain long-term benefit of fear extinction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6191435/ https://www.ncbi.nlm.nih.gov/pubmed/30327462 http://dx.doi.org/10.1038/s41467-018-06785-y |
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