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Compound stimulus extinction reduces spontaneous recovery in humans
Fear-related behaviors are prone to relapse following extinction. We tested in humans a compound extinction design (“deepened extinction”) shown in animal studies to reduce post-extinction fear recovery. Adult subjects underwent fear conditioning to a visual and an auditory conditioned stimulus (CSA...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749731/ https://www.ncbi.nlm.nih.gov/pubmed/26572649 http://dx.doi.org/10.1101/lm.039479.115 |
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author | Coelho, Cesar A.O. Dunsmoor, Joseph E. Phelps, Elizabeth A. |
author_facet | Coelho, Cesar A.O. Dunsmoor, Joseph E. Phelps, Elizabeth A. |
author_sort | Coelho, Cesar A.O. |
collection | PubMed |
description | Fear-related behaviors are prone to relapse following extinction. We tested in humans a compound extinction design (“deepened extinction”) shown in animal studies to reduce post-extinction fear recovery. Adult subjects underwent fear conditioning to a visual and an auditory conditioned stimulus (CSA and CSB, respectively) separately paired with an electric shock. The target CS (CSA) was extinguished alone followed by compound presentations of the extinguished CSA and nonextinguished CSB. Recovery of conditioned skin conductance responses to CSA was reduced 24 h after compound extinction, as compared with a group who received an equal number of extinction trials to the CSA alone. |
format | Online Article Text |
id | pubmed-4749731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47497312016-12-01 Compound stimulus extinction reduces spontaneous recovery in humans Coelho, Cesar A.O. Dunsmoor, Joseph E. Phelps, Elizabeth A. Learn Mem Brief Communication Fear-related behaviors are prone to relapse following extinction. We tested in humans a compound extinction design (“deepened extinction”) shown in animal studies to reduce post-extinction fear recovery. Adult subjects underwent fear conditioning to a visual and an auditory conditioned stimulus (CSA and CSB, respectively) separately paired with an electric shock. The target CS (CSA) was extinguished alone followed by compound presentations of the extinguished CSA and nonextinguished CSB. Recovery of conditioned skin conductance responses to CSA was reduced 24 h after compound extinction, as compared with a group who received an equal number of extinction trials to the CSA alone. Cold Spring Harbor Laboratory Press 2015-12 /pmc/articles/PMC4749731/ /pubmed/26572649 http://dx.doi.org/10.1101/lm.039479.115 Text en © 2015 Coelho et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Brief Communication Coelho, Cesar A.O. Dunsmoor, Joseph E. Phelps, Elizabeth A. Compound stimulus extinction reduces spontaneous recovery in humans |
title | Compound stimulus extinction reduces spontaneous recovery in humans |
title_full | Compound stimulus extinction reduces spontaneous recovery in humans |
title_fullStr | Compound stimulus extinction reduces spontaneous recovery in humans |
title_full_unstemmed | Compound stimulus extinction reduces spontaneous recovery in humans |
title_short | Compound stimulus extinction reduces spontaneous recovery in humans |
title_sort | compound stimulus extinction reduces spontaneous recovery in humans |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749731/ https://www.ncbi.nlm.nih.gov/pubmed/26572649 http://dx.doi.org/10.1101/lm.039479.115 |
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