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Dopaminergic Plasticity in the Bilateral Hippocampus Following Threat Reversal in Humans
When a cue no longer predicts a threat, a diminished ability to extinguish or reverse this association is thought to increase risk for stress-related disorders. Despite the clear clinical relevance, the mediating neurochemical mechanisms of threat reversal have received relatively little study. One...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203150/ https://www.ncbi.nlm.nih.gov/pubmed/32376865 http://dx.doi.org/10.1038/s41598-020-63977-7 |
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author | Lissemore, Jennifer I. Nagano-Saito, Atsuko Smart, Kelly Gravel, Paul Leyton, Marco Benkelfat, Chawki |
author_facet | Lissemore, Jennifer I. Nagano-Saito, Atsuko Smart, Kelly Gravel, Paul Leyton, Marco Benkelfat, Chawki |
author_sort | Lissemore, Jennifer I. |
collection | PubMed |
description | When a cue no longer predicts a threat, a diminished ability to extinguish or reverse this association is thought to increase risk for stress-related disorders. Despite the clear clinical relevance, the mediating neurochemical mechanisms of threat reversal have received relatively little study. One neurotransmitter implicated in rodent research of changing associations with threat is dopamine. To study whether dopamine is involved in threat reversal in humans, we used high-resolution positron emission tomography (PET) coupled with (18)F-fallypride. Twelve healthy volunteers (6 F/6 M) underwent three PET scans: (i) at baseline, (ii) following threat conditioning (the response to a cue associated with electric wrist shock), and (iii) following threat reversal (the response to the same cue now associated with safety). We observed moderate evidence of reduced dopamine D2/3 receptor availability, consistent with greater dopamine release, in the bilateral anterior hippocampus following threat reversal, in response to a safety cue that was previously associated with threat, as compared to both baseline and during exposure to the same cue prior to threat reversal. These findings offer the first preliminary evidence that the response to a previously threatening cue that has since become associated with safety involves dopaminergic neurotransmission within the hippocampus in healthy humans. |
format | Online Article Text |
id | pubmed-7203150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72031502020-05-12 Dopaminergic Plasticity in the Bilateral Hippocampus Following Threat Reversal in Humans Lissemore, Jennifer I. Nagano-Saito, Atsuko Smart, Kelly Gravel, Paul Leyton, Marco Benkelfat, Chawki Sci Rep Article When a cue no longer predicts a threat, a diminished ability to extinguish or reverse this association is thought to increase risk for stress-related disorders. Despite the clear clinical relevance, the mediating neurochemical mechanisms of threat reversal have received relatively little study. One neurotransmitter implicated in rodent research of changing associations with threat is dopamine. To study whether dopamine is involved in threat reversal in humans, we used high-resolution positron emission tomography (PET) coupled with (18)F-fallypride. Twelve healthy volunteers (6 F/6 M) underwent three PET scans: (i) at baseline, (ii) following threat conditioning (the response to a cue associated with electric wrist shock), and (iii) following threat reversal (the response to the same cue now associated with safety). We observed moderate evidence of reduced dopamine D2/3 receptor availability, consistent with greater dopamine release, in the bilateral anterior hippocampus following threat reversal, in response to a safety cue that was previously associated with threat, as compared to both baseline and during exposure to the same cue prior to threat reversal. These findings offer the first preliminary evidence that the response to a previously threatening cue that has since become associated with safety involves dopaminergic neurotransmission within the hippocampus in healthy humans. Nature Publishing Group UK 2020-05-06 /pmc/articles/PMC7203150/ /pubmed/32376865 http://dx.doi.org/10.1038/s41598-020-63977-7 Text en © The Author(s) 2020 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 Lissemore, Jennifer I. Nagano-Saito, Atsuko Smart, Kelly Gravel, Paul Leyton, Marco Benkelfat, Chawki Dopaminergic Plasticity in the Bilateral Hippocampus Following Threat Reversal in Humans |
title | Dopaminergic Plasticity in the Bilateral Hippocampus Following Threat Reversal in Humans |
title_full | Dopaminergic Plasticity in the Bilateral Hippocampus Following Threat Reversal in Humans |
title_fullStr | Dopaminergic Plasticity in the Bilateral Hippocampus Following Threat Reversal in Humans |
title_full_unstemmed | Dopaminergic Plasticity in the Bilateral Hippocampus Following Threat Reversal in Humans |
title_short | Dopaminergic Plasticity in the Bilateral Hippocampus Following Threat Reversal in Humans |
title_sort | dopaminergic plasticity in the bilateral hippocampus following threat reversal in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203150/ https://www.ncbi.nlm.nih.gov/pubmed/32376865 http://dx.doi.org/10.1038/s41598-020-63977-7 |
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