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Diurnal Variation in Trigeminal Pain Sensitivity in Mice
Management of time and circadian disruption is an extremely important factor in basic research on pain and analgesia. Although pain is known to vary throughout the day, the mechanism underlying this circadian variation remains largely unknown. In this study, we hypothesized that the process of pain...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365185/ https://www.ncbi.nlm.nih.gov/pubmed/34408624 http://dx.doi.org/10.3389/fnins.2021.703440 |
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author | Niiro, Ayako Ohno, Sachi N. Yamagata, Kanae A. Yamagata, Kazuaki Tomita, Kazuo Kuramoto, Eriko Oda, Yoshiaki Nakamura, Takahiro J. Nakamura, Wataru Sugimura, Mitsutaka |
author_facet | Niiro, Ayako Ohno, Sachi N. Yamagata, Kanae A. Yamagata, Kazuaki Tomita, Kazuo Kuramoto, Eriko Oda, Yoshiaki Nakamura, Takahiro J. Nakamura, Wataru Sugimura, Mitsutaka |
author_sort | Niiro, Ayako |
collection | PubMed |
description | Management of time and circadian disruption is an extremely important factor in basic research on pain and analgesia. Although pain is known to vary throughout the day, the mechanism underlying this circadian variation remains largely unknown. In this study, we hypothesized that the process of pain transmission to the central nervous system (after receiving nociceptive stimuli from outside the body) would show day-night differences. Ten-week-old male mice were kept under a strict 12/12-h light/dark cycle for at least 10 days. Formalin was then injected into the second branch region of the trigeminal nerve and the duration of pain-related behaviors (PRBs) was assessed. Immunohistochemical staining was then performed, and the c-Fos-immunopositive cells in the trigeminal spinal tract subnucleus caudalis (Sp5C) were counted. The results showed that the duration of PRBs was longer and the number of c-Fos immunopositive cells in the Sp5C was higher at nighttime than during the day. In addition, the trigeminal ganglia (TG) were extracted from the mice and examined by quantitative real-time PCR to evaluate the daytime and nighttime expression of nociceptive receptors. The results showed that the mRNA expression of transient receptor potential ankyrin 1 in the TG was significantly higher at night than during the day. These results suggest that pain in the trigeminal nerve region is more intense at nighttime, when rodents are active, than during the daytime, partly due to differences in nociceptor expression. |
format | Online Article Text |
id | pubmed-8365185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83651852021-08-17 Diurnal Variation in Trigeminal Pain Sensitivity in Mice Niiro, Ayako Ohno, Sachi N. Yamagata, Kanae A. Yamagata, Kazuaki Tomita, Kazuo Kuramoto, Eriko Oda, Yoshiaki Nakamura, Takahiro J. Nakamura, Wataru Sugimura, Mitsutaka Front Neurosci Neuroscience Management of time and circadian disruption is an extremely important factor in basic research on pain and analgesia. Although pain is known to vary throughout the day, the mechanism underlying this circadian variation remains largely unknown. In this study, we hypothesized that the process of pain transmission to the central nervous system (after receiving nociceptive stimuli from outside the body) would show day-night differences. Ten-week-old male mice were kept under a strict 12/12-h light/dark cycle for at least 10 days. Formalin was then injected into the second branch region of the trigeminal nerve and the duration of pain-related behaviors (PRBs) was assessed. Immunohistochemical staining was then performed, and the c-Fos-immunopositive cells in the trigeminal spinal tract subnucleus caudalis (Sp5C) were counted. The results showed that the duration of PRBs was longer and the number of c-Fos immunopositive cells in the Sp5C was higher at nighttime than during the day. In addition, the trigeminal ganglia (TG) were extracted from the mice and examined by quantitative real-time PCR to evaluate the daytime and nighttime expression of nociceptive receptors. The results showed that the mRNA expression of transient receptor potential ankyrin 1 in the TG was significantly higher at night than during the day. These results suggest that pain in the trigeminal nerve region is more intense at nighttime, when rodents are active, than during the daytime, partly due to differences in nociceptor expression. Frontiers Media S.A. 2021-08-02 /pmc/articles/PMC8365185/ /pubmed/34408624 http://dx.doi.org/10.3389/fnins.2021.703440 Text en Copyright © 2021 Niiro, Ohno, Yamagata, Yamagata, Tomita, Kuramoto, Oda, Nakamura, Nakamura and Sugimura. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Niiro, Ayako Ohno, Sachi N. Yamagata, Kanae A. Yamagata, Kazuaki Tomita, Kazuo Kuramoto, Eriko Oda, Yoshiaki Nakamura, Takahiro J. Nakamura, Wataru Sugimura, Mitsutaka Diurnal Variation in Trigeminal Pain Sensitivity in Mice |
title | Diurnal Variation in Trigeminal Pain Sensitivity in Mice |
title_full | Diurnal Variation in Trigeminal Pain Sensitivity in Mice |
title_fullStr | Diurnal Variation in Trigeminal Pain Sensitivity in Mice |
title_full_unstemmed | Diurnal Variation in Trigeminal Pain Sensitivity in Mice |
title_short | Diurnal Variation in Trigeminal Pain Sensitivity in Mice |
title_sort | diurnal variation in trigeminal pain sensitivity in mice |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365185/ https://www.ncbi.nlm.nih.gov/pubmed/34408624 http://dx.doi.org/10.3389/fnins.2021.703440 |
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