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Connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury
BACKGROUND: Clinically, it is well known that injury of mandibular nerve fiber induces persistent ectopic pain which can spread to a wide area of the orofacial region innervated by the uninjured trigeminal nerve branches. However, the exact mechanism of such persistent ectopic orofacial pain is not...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955997/ https://www.ncbi.nlm.nih.gov/pubmed/27030716 http://dx.doi.org/10.1177/1744806916633704 |
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author | Kaji, Kaori Shinoda, Masamichi Honda, Kuniya Unno, Syumpei Shimizu, Noriyoshi Iwata, Koichi |
author_facet | Kaji, Kaori Shinoda, Masamichi Honda, Kuniya Unno, Syumpei Shimizu, Noriyoshi Iwata, Koichi |
author_sort | Kaji, Kaori |
collection | PubMed |
description | BACKGROUND: Clinically, it is well known that injury of mandibular nerve fiber induces persistent ectopic pain which can spread to a wide area of the orofacial region innervated by the uninjured trigeminal nerve branches. However, the exact mechanism of such persistent ectopic orofacial pain is not still known. The present study was undertaken to determine the role of connexin 43 in the trigeminal ganglion on mechanical hypersensitivity in rat whisker pad skin induced by inferior alveolar nerve injury. Here, we examined changes in orofacial mechanical sensitivity following inferior alveolar nerve injury. Furthermore, changes in connexin 43 expression in the trigeminal ganglion and its localization in the trigeminal ganglion were also examined. In addition, we investigated the functional significance of connexin 43 in relation to mechanical allodynia by using a selective gap junction blocker (Gap27). RESULTS: Long-lasting mechanical allodynia in the whisker pad skin and the upper eyelid skin, and activation of satellite glial cells in the trigeminal ganglion, were induced after inferior alveolar nerve injury. Connexin 43 was expressed in the activated satellite glial cells encircling trigeminal ganglion neurons innervating the whisker pad skin, and the connexin 43 protein expression was significantly increased after inferior alveolar nerve injury. Administration of Gap27 in the trigeminal ganglion significantly reduced satellite glial cell activation and mechanical hypersensitivity in the whisker pad skin. Moreover, the marked activation of satellite glial cells encircling trigeminal ganglion neurons innervating the whisker pad skin following inferior alveolar nerve injury implies that the satellite glial cell activation exerts a major influence on the excitability of nociceptive trigeminal ganglion neurons. CONCLUSIONS: These findings indicate that the propagation of satellite glial cell activation throughout the trigeminal ganglion via gap junctions, which are composed of connexin 43, plays a pivotal role in ectopic mechanical hypersensitivity in whisker pad skin following inferior alveolar nerve injury. |
format | Online Article Text |
id | pubmed-4955997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-49559972016-08-12 Connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury Kaji, Kaori Shinoda, Masamichi Honda, Kuniya Unno, Syumpei Shimizu, Noriyoshi Iwata, Koichi Mol Pain Research Article BACKGROUND: Clinically, it is well known that injury of mandibular nerve fiber induces persistent ectopic pain which can spread to a wide area of the orofacial region innervated by the uninjured trigeminal nerve branches. However, the exact mechanism of such persistent ectopic orofacial pain is not still known. The present study was undertaken to determine the role of connexin 43 in the trigeminal ganglion on mechanical hypersensitivity in rat whisker pad skin induced by inferior alveolar nerve injury. Here, we examined changes in orofacial mechanical sensitivity following inferior alveolar nerve injury. Furthermore, changes in connexin 43 expression in the trigeminal ganglion and its localization in the trigeminal ganglion were also examined. In addition, we investigated the functional significance of connexin 43 in relation to mechanical allodynia by using a selective gap junction blocker (Gap27). RESULTS: Long-lasting mechanical allodynia in the whisker pad skin and the upper eyelid skin, and activation of satellite glial cells in the trigeminal ganglion, were induced after inferior alveolar nerve injury. Connexin 43 was expressed in the activated satellite glial cells encircling trigeminal ganglion neurons innervating the whisker pad skin, and the connexin 43 protein expression was significantly increased after inferior alveolar nerve injury. Administration of Gap27 in the trigeminal ganglion significantly reduced satellite glial cell activation and mechanical hypersensitivity in the whisker pad skin. Moreover, the marked activation of satellite glial cells encircling trigeminal ganglion neurons innervating the whisker pad skin following inferior alveolar nerve injury implies that the satellite glial cell activation exerts a major influence on the excitability of nociceptive trigeminal ganglion neurons. CONCLUSIONS: These findings indicate that the propagation of satellite glial cell activation throughout the trigeminal ganglion via gap junctions, which are composed of connexin 43, plays a pivotal role in ectopic mechanical hypersensitivity in whisker pad skin following inferior alveolar nerve injury. SAGE Publications 2016-03-29 /pmc/articles/PMC4955997/ /pubmed/27030716 http://dx.doi.org/10.1177/1744806916633704 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Kaji, Kaori Shinoda, Masamichi Honda, Kuniya Unno, Syumpei Shimizu, Noriyoshi Iwata, Koichi Connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury |
title | Connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury |
title_full | Connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury |
title_fullStr | Connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury |
title_full_unstemmed | Connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury |
title_short | Connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury |
title_sort | connexin 43 contributes to ectopic orofacial pain following inferior alveolar nerve injury |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955997/ https://www.ncbi.nlm.nih.gov/pubmed/27030716 http://dx.doi.org/10.1177/1744806916633704 |
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