Cargando…

Promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training

Inhibiting fear-related thoughts and defensive behaviors when they are no longer appropriate to the situation is a prerequisite for flexible and adaptive responding to changing environments. Such inhibition of defensive systems is mediated by ventromedial prefrontal cortex (vmPFC), limbic basolatera...

Descripción completa

Detalles Bibliográficos
Autores principales: Szeska, Christoph, Richter, Jan, Wendt, Julia, Weymar, Mathias, Hamm, Alfons O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992620/
https://www.ncbi.nlm.nih.gov/pubmed/32001763
http://dx.doi.org/10.1038/s41598-020-58412-w
_version_ 1783492867606446080
author Szeska, Christoph
Richter, Jan
Wendt, Julia
Weymar, Mathias
Hamm, Alfons O.
author_facet Szeska, Christoph
Richter, Jan
Wendt, Julia
Weymar, Mathias
Hamm, Alfons O.
author_sort Szeska, Christoph
collection PubMed
description Inhibiting fear-related thoughts and defensive behaviors when they are no longer appropriate to the situation is a prerequisite for flexible and adaptive responding to changing environments. Such inhibition of defensive systems is mediated by ventromedial prefrontal cortex (vmPFC), limbic basolateral amygdala (BLA), and brain stem locus-coeruleus noradrenergic system (LC-NAs). Non-invasive, transcutaneous vagus nerve stimulation (tVNS) has shown to activate this circuit. Using a multiple-day single-cue fear conditioning and extinction paradigm, we investigated long-term effects of tVNS on inhibition of low-level amygdala modulated fear potentiated startle and cognitive risk assessments. We found that administration of tVNS during extinction training facilitated inhibition of fear potentiated startle responses and cognitive risk assessments, resulting in facilitated formation, consolidation and long-term recall of extinction memory, and prevention of the return of fear. These findings might indicate new ways to increase the efficacy of exposure-based treatments of anxiety disorders.
format Online
Article
Text
id pubmed-6992620
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-69926202020-02-05 Promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training Szeska, Christoph Richter, Jan Wendt, Julia Weymar, Mathias Hamm, Alfons O. Sci Rep Article Inhibiting fear-related thoughts and defensive behaviors when they are no longer appropriate to the situation is a prerequisite for flexible and adaptive responding to changing environments. Such inhibition of defensive systems is mediated by ventromedial prefrontal cortex (vmPFC), limbic basolateral amygdala (BLA), and brain stem locus-coeruleus noradrenergic system (LC-NAs). Non-invasive, transcutaneous vagus nerve stimulation (tVNS) has shown to activate this circuit. Using a multiple-day single-cue fear conditioning and extinction paradigm, we investigated long-term effects of tVNS on inhibition of low-level amygdala modulated fear potentiated startle and cognitive risk assessments. We found that administration of tVNS during extinction training facilitated inhibition of fear potentiated startle responses and cognitive risk assessments, resulting in facilitated formation, consolidation and long-term recall of extinction memory, and prevention of the return of fear. These findings might indicate new ways to increase the efficacy of exposure-based treatments of anxiety disorders. Nature Publishing Group UK 2020-01-30 /pmc/articles/PMC6992620/ /pubmed/32001763 http://dx.doi.org/10.1038/s41598-020-58412-w 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
Szeska, Christoph
Richter, Jan
Wendt, Julia
Weymar, Mathias
Hamm, Alfons O.
Promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training
title Promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training
title_full Promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training
title_fullStr Promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training
title_full_unstemmed Promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training
title_short Promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training
title_sort promoting long-term inhibition of human fear responses by non-invasive transcutaneous vagus nerve stimulation during extinction training
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992620/
https://www.ncbi.nlm.nih.gov/pubmed/32001763
http://dx.doi.org/10.1038/s41598-020-58412-w
work_keys_str_mv AT szeskachristoph promotinglongterminhibitionofhumanfearresponsesbynoninvasivetranscutaneousvagusnervestimulationduringextinctiontraining
AT richterjan promotinglongterminhibitionofhumanfearresponsesbynoninvasivetranscutaneousvagusnervestimulationduringextinctiontraining
AT wendtjulia promotinglongterminhibitionofhumanfearresponsesbynoninvasivetranscutaneousvagusnervestimulationduringextinctiontraining
AT weymarmathias promotinglongterminhibitionofhumanfearresponsesbynoninvasivetranscutaneousvagusnervestimulationduringextinctiontraining
AT hammalfonso promotinglongterminhibitionofhumanfearresponsesbynoninvasivetranscutaneousvagusnervestimulationduringextinctiontraining