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Mechanisms Underlying Ectopic Persistent Tooth-Pulp Pain following Pulpal Inflammation

In order to clarify the peripheral mechanisms of ectopic persistent pain in a tooth pulp following pulpal inflammation of an adjacent tooth, masseter muscle activity, phosphorylated extracellular signal-regulated protein kinase (pERK) and TRPV1 immunohistochemistries and satellite cell activation us...

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Autores principales: Matsuura, Shingo, Shimizu, Kohei, Shinoda, Masamichi, Ohara, Kinuyo, Ogiso, Bunnai, Honda, Kuniya, Katagiri, Ayano, Sessle, Barry J., Urata, Kentaro, Iwata, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547043/
https://www.ncbi.nlm.nih.gov/pubmed/23341909
http://dx.doi.org/10.1371/journal.pone.0052840
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author Matsuura, Shingo
Shimizu, Kohei
Shinoda, Masamichi
Ohara, Kinuyo
Ogiso, Bunnai
Honda, Kuniya
Katagiri, Ayano
Sessle, Barry J.
Urata, Kentaro
Iwata, Koichi
author_facet Matsuura, Shingo
Shimizu, Kohei
Shinoda, Masamichi
Ohara, Kinuyo
Ogiso, Bunnai
Honda, Kuniya
Katagiri, Ayano
Sessle, Barry J.
Urata, Kentaro
Iwata, Koichi
author_sort Matsuura, Shingo
collection PubMed
description In order to clarify the peripheral mechanisms of ectopic persistent pain in a tooth pulp following pulpal inflammation of an adjacent tooth, masseter muscle activity, phosphorylated extracellular signal-regulated protein kinase (pERK) and TRPV1 immunohistochemistries and satellite cell activation using glial fibrillary acidic protein (GFAP) immunohistochemistry in the trigeminal ganglion (TG) were studied in the rats with molar tooth-pulp inflammation. And, Fluorogold (FG) and DiI were also used in a neuronal tracing study to analyze if some TG neurons innervate more than one tooth pulp. Complete Freund’s adjuvant (CFA) or saline was applied into the upper first molar tooth pulp (M1) in pentobarbital-anesthetized rats, and capsaicin was applied into the upper second molar tooth pulp (M2) on day 3 after the CFA or saline application. Mean EMG activity elicited in the masseter muscle by capsaicin application to M2 was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats. The mean number of pERK-immunoreactive (IR) TG cells was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats. Application of the satellite cell inhibitor fluorocitrate (FC) into TG caused a significant depression of capsaicin-induced masseter muscle activity and a significant reduction of satellite cell activation. The number of TRPV1-IR TG cells innervating M2 was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats, and that was decreased following FC injection into TG. Furthermore, 6% of TG neurons innervating M1 and/or M2 innervated both M1 and M2. These findings suggest that satellite cell activation following tooth pulp inflammation and innervation of multiple tooth pulps by single TG neurons may be involved in the enhancement of the activity of TG neurons innervating adjacent non-inflamed teeth that also show enhancement of TRPV1 expression in TG neurons, resulting in the ectopic persistent tooth-pulp pain following pulpal inflammation of adjacent teeth.
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spelling pubmed-35470432013-01-22 Mechanisms Underlying Ectopic Persistent Tooth-Pulp Pain following Pulpal Inflammation Matsuura, Shingo Shimizu, Kohei Shinoda, Masamichi Ohara, Kinuyo Ogiso, Bunnai Honda, Kuniya Katagiri, Ayano Sessle, Barry J. Urata, Kentaro Iwata, Koichi PLoS One Research Article In order to clarify the peripheral mechanisms of ectopic persistent pain in a tooth pulp following pulpal inflammation of an adjacent tooth, masseter muscle activity, phosphorylated extracellular signal-regulated protein kinase (pERK) and TRPV1 immunohistochemistries and satellite cell activation using glial fibrillary acidic protein (GFAP) immunohistochemistry in the trigeminal ganglion (TG) were studied in the rats with molar tooth-pulp inflammation. And, Fluorogold (FG) and DiI were also used in a neuronal tracing study to analyze if some TG neurons innervate more than one tooth pulp. Complete Freund’s adjuvant (CFA) or saline was applied into the upper first molar tooth pulp (M1) in pentobarbital-anesthetized rats, and capsaicin was applied into the upper second molar tooth pulp (M2) on day 3 after the CFA or saline application. Mean EMG activity elicited in the masseter muscle by capsaicin application to M2 was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats. The mean number of pERK-immunoreactive (IR) TG cells was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats. Application of the satellite cell inhibitor fluorocitrate (FC) into TG caused a significant depression of capsaicin-induced masseter muscle activity and a significant reduction of satellite cell activation. The number of TRPV1-IR TG cells innervating M2 was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats, and that was decreased following FC injection into TG. Furthermore, 6% of TG neurons innervating M1 and/or M2 innervated both M1 and M2. These findings suggest that satellite cell activation following tooth pulp inflammation and innervation of multiple tooth pulps by single TG neurons may be involved in the enhancement of the activity of TG neurons innervating adjacent non-inflamed teeth that also show enhancement of TRPV1 expression in TG neurons, resulting in the ectopic persistent tooth-pulp pain following pulpal inflammation of adjacent teeth. Public Library of Science 2013-01-16 /pmc/articles/PMC3547043/ /pubmed/23341909 http://dx.doi.org/10.1371/journal.pone.0052840 Text en © 2013 Matsuura et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Matsuura, Shingo
Shimizu, Kohei
Shinoda, Masamichi
Ohara, Kinuyo
Ogiso, Bunnai
Honda, Kuniya
Katagiri, Ayano
Sessle, Barry J.
Urata, Kentaro
Iwata, Koichi
Mechanisms Underlying Ectopic Persistent Tooth-Pulp Pain following Pulpal Inflammation
title Mechanisms Underlying Ectopic Persistent Tooth-Pulp Pain following Pulpal Inflammation
title_full Mechanisms Underlying Ectopic Persistent Tooth-Pulp Pain following Pulpal Inflammation
title_fullStr Mechanisms Underlying Ectopic Persistent Tooth-Pulp Pain following Pulpal Inflammation
title_full_unstemmed Mechanisms Underlying Ectopic Persistent Tooth-Pulp Pain following Pulpal Inflammation
title_short Mechanisms Underlying Ectopic Persistent Tooth-Pulp Pain following Pulpal Inflammation
title_sort mechanisms underlying ectopic persistent tooth-pulp pain following pulpal inflammation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547043/
https://www.ncbi.nlm.nih.gov/pubmed/23341909
http://dx.doi.org/10.1371/journal.pone.0052840
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