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Limbic and cortical control of phonation for speech in response to a public speech preparation stressor
Knowledge on brain networks subserving vocalization in vocally healthy individuals under various task conditions is scarce but paramount to understand voice disorders. The aims of our study were to determine (1) the effect of social-evaluative stress on the central neural control of phonation underl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572327/ https://www.ncbi.nlm.nih.gov/pubmed/31049806 http://dx.doi.org/10.1007/s11682-019-00102-x |
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author | Dietrich, Maria Andreatta, Richard D. Jiang, Yang Stemple, Joseph C. |
author_facet | Dietrich, Maria Andreatta, Richard D. Jiang, Yang Stemple, Joseph C. |
author_sort | Dietrich, Maria |
collection | PubMed |
description | Knowledge on brain networks subserving vocalization in vocally healthy individuals under various task conditions is scarce but paramount to understand voice disorders. The aims of our study were to determine (1) the effect of social-evaluative stress on the central neural control of phonation underlying speech production; and (2) the neural signature, personality profile, and aerodynamic vocal function in relation to salivary cortisol responses. Thirteen vocally healthy females underwent an event-related sparse-sampling fMRI protocol consisting of voiced and whispered sentence productions with and without exposure to the social-evaluative stressor public speaking anticipation. Participants completed a personality questionnaire, rating scales of negative emotional state, and provided salivary cortisol samples. In the total sample, the task contrast of voiced productions revealed that stressor exposure resulted in a peak activation in the right caudate with concomitant deactivations in the bilateral pgACC and aMCC, and right IFG, BA 9, BA 10, insula, putamen, and thalamus. There were individual differences in stressor-induced brain activations as a function of stress reactivity with greater cortisol reactivity linked with lower laryngeal motor cortex activity and lower scores on aspects of extraversion. Our data confirm that stress alters the phonatory control for speech production through limbic-motor interactions. The findings support the Trait Theory of Voice Disorders (Roy and Bless 2000) and help provide critical insights to the study of voice disorders such as primary muscle tension dysphonia. |
format | Online Article Text |
id | pubmed-7572327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-75723272020-10-20 Limbic and cortical control of phonation for speech in response to a public speech preparation stressor Dietrich, Maria Andreatta, Richard D. Jiang, Yang Stemple, Joseph C. Brain Imaging Behav Original Research Knowledge on brain networks subserving vocalization in vocally healthy individuals under various task conditions is scarce but paramount to understand voice disorders. The aims of our study were to determine (1) the effect of social-evaluative stress on the central neural control of phonation underlying speech production; and (2) the neural signature, personality profile, and aerodynamic vocal function in relation to salivary cortisol responses. Thirteen vocally healthy females underwent an event-related sparse-sampling fMRI protocol consisting of voiced and whispered sentence productions with and without exposure to the social-evaluative stressor public speaking anticipation. Participants completed a personality questionnaire, rating scales of negative emotional state, and provided salivary cortisol samples. In the total sample, the task contrast of voiced productions revealed that stressor exposure resulted in a peak activation in the right caudate with concomitant deactivations in the bilateral pgACC and aMCC, and right IFG, BA 9, BA 10, insula, putamen, and thalamus. There were individual differences in stressor-induced brain activations as a function of stress reactivity with greater cortisol reactivity linked with lower laryngeal motor cortex activity and lower scores on aspects of extraversion. Our data confirm that stress alters the phonatory control for speech production through limbic-motor interactions. The findings support the Trait Theory of Voice Disorders (Roy and Bless 2000) and help provide critical insights to the study of voice disorders such as primary muscle tension dysphonia. Springer US 2019-05-02 2020 /pmc/articles/PMC7572327/ /pubmed/31049806 http://dx.doi.org/10.1007/s11682-019-00102-x Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Research Dietrich, Maria Andreatta, Richard D. Jiang, Yang Stemple, Joseph C. Limbic and cortical control of phonation for speech in response to a public speech preparation stressor |
title | Limbic and cortical control of phonation for speech in response to a public speech preparation stressor |
title_full | Limbic and cortical control of phonation for speech in response to a public speech preparation stressor |
title_fullStr | Limbic and cortical control of phonation for speech in response to a public speech preparation stressor |
title_full_unstemmed | Limbic and cortical control of phonation for speech in response to a public speech preparation stressor |
title_short | Limbic and cortical control of phonation for speech in response to a public speech preparation stressor |
title_sort | limbic and cortical control of phonation for speech in response to a public speech preparation stressor |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572327/ https://www.ncbi.nlm.nih.gov/pubmed/31049806 http://dx.doi.org/10.1007/s11682-019-00102-x |
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