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Facial expressions of pain: the role of the serotonergic system

RATIONALE: Although interest in the neurobiology of facial communication of pain has increased over the last decades, little is known about which neurotransmitter systems might be involved in regulating facial expressions of pain. OBJECTIVES: We aim to investigate whether the serotonergic system (5-...

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Autores principales: Kunz, Miriam, Bär, Karl-Jürgen, Karmann, Anna J., Wagner, Gerd, Lautenbacher, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10640419/
https://www.ncbi.nlm.nih.gov/pubmed/37676276
http://dx.doi.org/10.1007/s00213-023-06455-y
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author Kunz, Miriam
Bär, Karl-Jürgen
Karmann, Anna J.
Wagner, Gerd
Lautenbacher, Stefan
author_facet Kunz, Miriam
Bär, Karl-Jürgen
Karmann, Anna J.
Wagner, Gerd
Lautenbacher, Stefan
author_sort Kunz, Miriam
collection PubMed
description RATIONALE: Although interest in the neurobiology of facial communication of pain has increased over the last decades, little is known about which neurotransmitter systems might be involved in regulating facial expressions of pain. OBJECTIVES: We aim to investigate whether the serotonergic system (5-HT), which has been implicated in various aspects of pain processing as well as in behavioral response inhibition, might play a role in facial expressions of pain. Using acute tryptophan depletion (ATD) to manipulate 5-HT function, we examined its effects on facial and subjective pain responses. METHODS: In a double-blind, placebo-controlled within-subject design, 27 participants received either an ATD or a control drink in two separate sessions. Approximately 5-h post-oral consumption, we assessed pain thresholds (heat, pressure) as well as facial and subjective responses to phasic heat pain. Moreover, situational pain catastrophizing and mood were assessed as affective state indicators. RESULTS: ATD neither influenced pain thresholds nor self-report ratings, nor catastrophizing or mood. Only facial responses were significantly affected by ATD. ATD led to a decrease in pain-indicative as well as in pain-non-indicative facial responses to painful heat, compared to the control condition. CONCLUSIONS: Decrease in brain 5-HT synthesis via ATD significantly reduced facial responses to phasic heat pain; possibly due to (i) diminished disposition to display social behavior or due to (ii) decreased facilitation of excitatory inputs to the facial motor neuron.
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spelling pubmed-106404192023-11-14 Facial expressions of pain: the role of the serotonergic system Kunz, Miriam Bär, Karl-Jürgen Karmann, Anna J. Wagner, Gerd Lautenbacher, Stefan Psychopharmacology (Berl) Original Investigation RATIONALE: Although interest in the neurobiology of facial communication of pain has increased over the last decades, little is known about which neurotransmitter systems might be involved in regulating facial expressions of pain. OBJECTIVES: We aim to investigate whether the serotonergic system (5-HT), which has been implicated in various aspects of pain processing as well as in behavioral response inhibition, might play a role in facial expressions of pain. Using acute tryptophan depletion (ATD) to manipulate 5-HT function, we examined its effects on facial and subjective pain responses. METHODS: In a double-blind, placebo-controlled within-subject design, 27 participants received either an ATD or a control drink in two separate sessions. Approximately 5-h post-oral consumption, we assessed pain thresholds (heat, pressure) as well as facial and subjective responses to phasic heat pain. Moreover, situational pain catastrophizing and mood were assessed as affective state indicators. RESULTS: ATD neither influenced pain thresholds nor self-report ratings, nor catastrophizing or mood. Only facial responses were significantly affected by ATD. ATD led to a decrease in pain-indicative as well as in pain-non-indicative facial responses to painful heat, compared to the control condition. CONCLUSIONS: Decrease in brain 5-HT synthesis via ATD significantly reduced facial responses to phasic heat pain; possibly due to (i) diminished disposition to display social behavior or due to (ii) decreased facilitation of excitatory inputs to the facial motor neuron. Springer Berlin Heidelberg 2023-09-07 2023 /pmc/articles/PMC10640419/ /pubmed/37676276 http://dx.doi.org/10.1007/s00213-023-06455-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Investigation
Kunz, Miriam
Bär, Karl-Jürgen
Karmann, Anna J.
Wagner, Gerd
Lautenbacher, Stefan
Facial expressions of pain: the role of the serotonergic system
title Facial expressions of pain: the role of the serotonergic system
title_full Facial expressions of pain: the role of the serotonergic system
title_fullStr Facial expressions of pain: the role of the serotonergic system
title_full_unstemmed Facial expressions of pain: the role of the serotonergic system
title_short Facial expressions of pain: the role of the serotonergic system
title_sort facial expressions of pain: the role of the serotonergic system
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10640419/
https://www.ncbi.nlm.nih.gov/pubmed/37676276
http://dx.doi.org/10.1007/s00213-023-06455-y
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