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Excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a TMS-EEG study

Threat detection is essential for protecting individuals from adverse situations, in which a network of amygdala, limbic regions and dorsomedial prefrontal cortex (dmPFC) regions are involved in fear processing. Excitability regulation in the dmPFC might be crucial for fear processing, while abnorma...

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Autores principales: Gonzalez-Escamilla, Gabriel, Chirumamilla, Venkata C., Meyer, Benjamin, Bonertz, Tamara, von Grotthus, Sarah, Vogt, Johannes, Stroh, Albrecht, Horstmann, Johann-Philipp, Tüscher, Oliver, Kalisch, Raffael, Muthuraman, Muthuraman, Groppa, Sergiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162240/
https://www.ncbi.nlm.nih.gov/pubmed/30267020
http://dx.doi.org/10.1038/s41598-018-32781-9
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author Gonzalez-Escamilla, Gabriel
Chirumamilla, Venkata C.
Meyer, Benjamin
Bonertz, Tamara
von Grotthus, Sarah
Vogt, Johannes
Stroh, Albrecht
Horstmann, Johann-Philipp
Tüscher, Oliver
Kalisch, Raffael
Muthuraman, Muthuraman
Groppa, Sergiu
author_facet Gonzalez-Escamilla, Gabriel
Chirumamilla, Venkata C.
Meyer, Benjamin
Bonertz, Tamara
von Grotthus, Sarah
Vogt, Johannes
Stroh, Albrecht
Horstmann, Johann-Philipp
Tüscher, Oliver
Kalisch, Raffael
Muthuraman, Muthuraman
Groppa, Sergiu
author_sort Gonzalez-Escamilla, Gabriel
collection PubMed
description Threat detection is essential for protecting individuals from adverse situations, in which a network of amygdala, limbic regions and dorsomedial prefrontal cortex (dmPFC) regions are involved in fear processing. Excitability regulation in the dmPFC might be crucial for fear processing, while abnormal patterns could lead to mental illness. Notwithstanding, non-invasive paradigms to measure excitability regulation during fear processing in humans are missing. To address this challenge we adapted an approach for excitability characterization, combining electroencephalography (EEG) and transcranial magnetic stimulation (TMS) over the dmPFC during an instructed fear paradigm, to dynamically dissect its role in fear processing. Event-related (ERP) and TMS-evoked potentials (TEP) were analyzed to trace dmPFC excitability. We further linked the excitability regulation patterns to individual MRI-derived gray matter structural integrity of the fear network. Increased cortical excitability was demonstrated to threat (T) processing in comparison to no-threat (NT), reflected by increased amplitude of evoked potentials. Furthermore, TMS at dmPFC enhanced the evoked responses during T processing, while the structural integrity of the dmPFC and amygdala predicted the excitability regulation patterns to fear processing. The dmPFC takes a special role during fear processing by dynamically regulating excitability. The applied paradigm can be used to non-invasively track response abnormalities to threat stimuli in healthy subjects or patients with mental disorders.
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spelling pubmed-61622402018-10-02 Excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a TMS-EEG study Gonzalez-Escamilla, Gabriel Chirumamilla, Venkata C. Meyer, Benjamin Bonertz, Tamara von Grotthus, Sarah Vogt, Johannes Stroh, Albrecht Horstmann, Johann-Philipp Tüscher, Oliver Kalisch, Raffael Muthuraman, Muthuraman Groppa, Sergiu Sci Rep Article Threat detection is essential for protecting individuals from adverse situations, in which a network of amygdala, limbic regions and dorsomedial prefrontal cortex (dmPFC) regions are involved in fear processing. Excitability regulation in the dmPFC might be crucial for fear processing, while abnormal patterns could lead to mental illness. Notwithstanding, non-invasive paradigms to measure excitability regulation during fear processing in humans are missing. To address this challenge we adapted an approach for excitability characterization, combining electroencephalography (EEG) and transcranial magnetic stimulation (TMS) over the dmPFC during an instructed fear paradigm, to dynamically dissect its role in fear processing. Event-related (ERP) and TMS-evoked potentials (TEP) were analyzed to trace dmPFC excitability. We further linked the excitability regulation patterns to individual MRI-derived gray matter structural integrity of the fear network. Increased cortical excitability was demonstrated to threat (T) processing in comparison to no-threat (NT), reflected by increased amplitude of evoked potentials. Furthermore, TMS at dmPFC enhanced the evoked responses during T processing, while the structural integrity of the dmPFC and amygdala predicted the excitability regulation patterns to fear processing. The dmPFC takes a special role during fear processing by dynamically regulating excitability. The applied paradigm can be used to non-invasively track response abnormalities to threat stimuli in healthy subjects or patients with mental disorders. Nature Publishing Group UK 2018-09-28 /pmc/articles/PMC6162240/ /pubmed/30267020 http://dx.doi.org/10.1038/s41598-018-32781-9 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
Gonzalez-Escamilla, Gabriel
Chirumamilla, Venkata C.
Meyer, Benjamin
Bonertz, Tamara
von Grotthus, Sarah
Vogt, Johannes
Stroh, Albrecht
Horstmann, Johann-Philipp
Tüscher, Oliver
Kalisch, Raffael
Muthuraman, Muthuraman
Groppa, Sergiu
Excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a TMS-EEG study
title Excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a TMS-EEG study
title_full Excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a TMS-EEG study
title_fullStr Excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a TMS-EEG study
title_full_unstemmed Excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a TMS-EEG study
title_short Excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a TMS-EEG study
title_sort excitability regulation in the dorsomedial prefrontal cortex during sustained instructed fear responses: a tms-eeg study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162240/
https://www.ncbi.nlm.nih.gov/pubmed/30267020
http://dx.doi.org/10.1038/s41598-018-32781-9
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