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Transcutaneous vagus nerve stimulation and extinction of prepared fear: A conceptual non-replication
Transcutaneous stimulation of the auricular branch of the vagus nerve (tVNS) may accelerate fear extinction in healthy humans. Here, we aimed to investigate this hypothesis in healthy young participants in a prepared learning paradigm, using spider pictures as conditioned stimuli. After a fear condi...
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/PMC6068181/ https://www.ncbi.nlm.nih.gov/pubmed/30065275 http://dx.doi.org/10.1038/s41598-018-29561-w |
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author | Burger, Andreas M. Van Diest, Ilse van der Does, Willem Hysaj, Marsida Thayer, Julian F. Brosschot, Jos F. Verkuil, Bart |
author_facet | Burger, Andreas M. Van Diest, Ilse van der Does, Willem Hysaj, Marsida Thayer, Julian F. Brosschot, Jos F. Verkuil, Bart |
author_sort | Burger, Andreas M. |
collection | PubMed |
description | Transcutaneous stimulation of the auricular branch of the vagus nerve (tVNS) may accelerate fear extinction in healthy humans. Here, we aimed to investigate this hypothesis in healthy young participants in a prepared learning paradigm, using spider pictures as conditioned stimuli. After a fear conditioning phase, participants were randomly allocated to receive tVNS (final N = 42) or sham stimulation (final N = 43) during an extinction phase. Conditioned fear was assessed using US expectancy ratings, skin conductance and fear potentiated startle responses. After successful fear acquisition, participants in both groups showed a reduction of fear over the course of the extinction phase. There were no between-group differences in extinction rates for physiological indices of fear. Contrary to previous findings, participants in the tVNS condition also did not show accelerated declarative extinction learning. Participants in the tVNS condition did have lower initial US expectancy ratings for the CS− trials than those who received sham stimulation, which may indicate an enhanced processing of safety cues due to tVNS. In conclusion, the expected accelerated extinction due to tVNS was not observed. The results from this study call for more research on the optimal tVNS stimulation intensity settings. |
format | Online Article Text |
id | pubmed-6068181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60681812018-08-03 Transcutaneous vagus nerve stimulation and extinction of prepared fear: A conceptual non-replication Burger, Andreas M. Van Diest, Ilse van der Does, Willem Hysaj, Marsida Thayer, Julian F. Brosschot, Jos F. Verkuil, Bart Sci Rep Article Transcutaneous stimulation of the auricular branch of the vagus nerve (tVNS) may accelerate fear extinction in healthy humans. Here, we aimed to investigate this hypothesis in healthy young participants in a prepared learning paradigm, using spider pictures as conditioned stimuli. After a fear conditioning phase, participants were randomly allocated to receive tVNS (final N = 42) or sham stimulation (final N = 43) during an extinction phase. Conditioned fear was assessed using US expectancy ratings, skin conductance and fear potentiated startle responses. After successful fear acquisition, participants in both groups showed a reduction of fear over the course of the extinction phase. There were no between-group differences in extinction rates for physiological indices of fear. Contrary to previous findings, participants in the tVNS condition also did not show accelerated declarative extinction learning. Participants in the tVNS condition did have lower initial US expectancy ratings for the CS− trials than those who received sham stimulation, which may indicate an enhanced processing of safety cues due to tVNS. In conclusion, the expected accelerated extinction due to tVNS was not observed. The results from this study call for more research on the optimal tVNS stimulation intensity settings. Nature Publishing Group UK 2018-07-31 /pmc/articles/PMC6068181/ /pubmed/30065275 http://dx.doi.org/10.1038/s41598-018-29561-w 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 Burger, Andreas M. Van Diest, Ilse van der Does, Willem Hysaj, Marsida Thayer, Julian F. Brosschot, Jos F. Verkuil, Bart Transcutaneous vagus nerve stimulation and extinction of prepared fear: A conceptual non-replication |
title | Transcutaneous vagus nerve stimulation and extinction of prepared fear: A conceptual non-replication |
title_full | Transcutaneous vagus nerve stimulation and extinction of prepared fear: A conceptual non-replication |
title_fullStr | Transcutaneous vagus nerve stimulation and extinction of prepared fear: A conceptual non-replication |
title_full_unstemmed | Transcutaneous vagus nerve stimulation and extinction of prepared fear: A conceptual non-replication |
title_short | Transcutaneous vagus nerve stimulation and extinction of prepared fear: A conceptual non-replication |
title_sort | transcutaneous vagus nerve stimulation and extinction of prepared fear: a conceptual non-replication |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068181/ https://www.ncbi.nlm.nih.gov/pubmed/30065275 http://dx.doi.org/10.1038/s41598-018-29561-w |
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