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Drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants

Current pain classifications use 1.0-kg palpation of the masseter muscle to distinguish between “pain patients” and “healthy controls” but a thorough understanding of the normal physiological responses to various somatosensory stimuli is lacking. The aim of this study was to investigate somatosensor...

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Autores principales: Hayakawa, Hidetoshi, Iida, Takashi, Honda-Sakaki, Mika, Masuda, Manabu, Svensson, Peter, Komiyama, Osamu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136476/
https://www.ncbi.nlm.nih.gov/pubmed/34012096
http://dx.doi.org/10.1038/s41598-021-89937-3
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author Hayakawa, Hidetoshi
Iida, Takashi
Honda-Sakaki, Mika
Masuda, Manabu
Svensson, Peter
Komiyama, Osamu
author_facet Hayakawa, Hidetoshi
Iida, Takashi
Honda-Sakaki, Mika
Masuda, Manabu
Svensson, Peter
Komiyama, Osamu
author_sort Hayakawa, Hidetoshi
collection PubMed
description Current pain classifications use 1.0-kg palpation of the masseter muscle to distinguish between “pain patients” and “healthy controls” but a thorough understanding of the normal physiological responses to various somatosensory stimuli is lacking. The aim of this study was to investigate somatosensory function of the skin over the masseter muscle in healthy participants that were divided into a masseter pain prone group (MPP) (n = 22) and non-MPP group (n = 22), according to the response to a 1.0-kg palpation. Quantitative sensory testing (QST) was performed at the skin above the right masseter muscle (homotopic). In an additional experiment, 13 individuals each from MPP and non-MPP received application of 60% topical lidocaine tape to the skin over the masseter muscle for 30 min. Immediately after, mechanical pain sensitivity (MPS), dynamic mechanical allodynia, and pressure pain threshold were tested. Homotopic MPS was significantly higher and PPTs significantly lower in MPP than in N-MPP (P < 0.05). Strikingly, no other differences in QST outcomes were observed between the groups (P > 0.05). After lidocaine application, no significant differences in homotopic MPS were observed between groups. The presence or absence of acute provoked pain in masseter muscle is exclusively associated with differences in homotopic MPS which is decreased following topical anesthesia.
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spelling pubmed-81364762021-05-25 Drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants Hayakawa, Hidetoshi Iida, Takashi Honda-Sakaki, Mika Masuda, Manabu Svensson, Peter Komiyama, Osamu Sci Rep Article Current pain classifications use 1.0-kg palpation of the masseter muscle to distinguish between “pain patients” and “healthy controls” but a thorough understanding of the normal physiological responses to various somatosensory stimuli is lacking. The aim of this study was to investigate somatosensory function of the skin over the masseter muscle in healthy participants that were divided into a masseter pain prone group (MPP) (n = 22) and non-MPP group (n = 22), according to the response to a 1.0-kg palpation. Quantitative sensory testing (QST) was performed at the skin above the right masseter muscle (homotopic). In an additional experiment, 13 individuals each from MPP and non-MPP received application of 60% topical lidocaine tape to the skin over the masseter muscle for 30 min. Immediately after, mechanical pain sensitivity (MPS), dynamic mechanical allodynia, and pressure pain threshold were tested. Homotopic MPS was significantly higher and PPTs significantly lower in MPP than in N-MPP (P < 0.05). Strikingly, no other differences in QST outcomes were observed between the groups (P > 0.05). After lidocaine application, no significant differences in homotopic MPS were observed between groups. The presence or absence of acute provoked pain in masseter muscle is exclusively associated with differences in homotopic MPS which is decreased following topical anesthesia. Nature Publishing Group UK 2021-05-19 /pmc/articles/PMC8136476/ /pubmed/34012096 http://dx.doi.org/10.1038/s41598-021-89937-3 Text en © The Author(s) 2021 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 Article
Hayakawa, Hidetoshi
Iida, Takashi
Honda-Sakaki, Mika
Masuda, Manabu
Svensson, Peter
Komiyama, Osamu
Drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants
title Drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants
title_full Drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants
title_fullStr Drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants
title_full_unstemmed Drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants
title_short Drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants
title_sort drop homotopic effects of masseter-muscle pain on somatosensory sensitivity in healthy participants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136476/
https://www.ncbi.nlm.nih.gov/pubmed/34012096
http://dx.doi.org/10.1038/s41598-021-89937-3
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