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TRPV1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats

Pain in masticatory muscles is among the most prominent symptoms of temperomandibular disorders (TMDs) that have diverse and complex etiology. A common complaint of TMD is that unilateral pain of craniofacial muscle can cause a widespread of bilateral pain sensation, although the underlying mechanis...

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Autores principales: Simonic-Kocijan, Suncana, Zhao, Xuehong, Liu, Wen, Wu, Yuwei, Uhac, Ivone, Wang, KeWei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880456/
https://www.ncbi.nlm.nih.gov/pubmed/24377488
http://dx.doi.org/10.1186/1744-8069-9-68
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author Simonic-Kocijan, Suncana
Zhao, Xuehong
Liu, Wen
Wu, Yuwei
Uhac, Ivone
Wang, KeWei
author_facet Simonic-Kocijan, Suncana
Zhao, Xuehong
Liu, Wen
Wu, Yuwei
Uhac, Ivone
Wang, KeWei
author_sort Simonic-Kocijan, Suncana
collection PubMed
description Pain in masticatory muscles is among the most prominent symptoms of temperomandibular disorders (TMDs) that have diverse and complex etiology. A common complaint of TMD is that unilateral pain of craniofacial muscle can cause a widespread of bilateral pain sensation, although the underlying mechanism remains unknown. To investigate whether unilateral inflammation of masseter muscle can cause a bilateral allodynia, we generated masseter muscle inflammation induced by unilateral injection of complete Freund’s adjuvant (CFA) in rats, and measured the bilateral head withdrawal threshold at different time points using a von Frey anesthesiometer. After behavioral assessment, both right and left trigeminal ganglia (TRG) were dissected and examined for histopathology and transient receptor potential vanilloid 1 (TRPV1) mRNA expression using quantitative real-time PCR analysis. A significant increase in TRPV1 mRNA expression occurred in TRG ipsilateral to CFA injected masseter muscle, whereas no significant alteration in TRPV1 occurred in the contralateral TRG. Interestingly, central injection of TRPV1 antagonist 5-iodoresiniferatoxin into the hippocampus significantly attenuated the head withdrawal response of both CFA injected and non-CFA injected contralateral masseter muscle. Our findings show that unilateral inflammation of masseter muscle is capable of inducing bilateral allodynia in rats. Upregulation of TRPV1 at the TRG level is due to nociception caused by inflammation, whereas contralateral nocifensive behavior in masticatory muscle nociception is likely mediated by central TRPV1, pointing to the involvement of altered information processing in higher centers.
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spelling pubmed-38804562014-01-05 TRPV1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats Simonic-Kocijan, Suncana Zhao, Xuehong Liu, Wen Wu, Yuwei Uhac, Ivone Wang, KeWei Mol Pain Research Pain in masticatory muscles is among the most prominent symptoms of temperomandibular disorders (TMDs) that have diverse and complex etiology. A common complaint of TMD is that unilateral pain of craniofacial muscle can cause a widespread of bilateral pain sensation, although the underlying mechanism remains unknown. To investigate whether unilateral inflammation of masseter muscle can cause a bilateral allodynia, we generated masseter muscle inflammation induced by unilateral injection of complete Freund’s adjuvant (CFA) in rats, and measured the bilateral head withdrawal threshold at different time points using a von Frey anesthesiometer. After behavioral assessment, both right and left trigeminal ganglia (TRG) were dissected and examined for histopathology and transient receptor potential vanilloid 1 (TRPV1) mRNA expression using quantitative real-time PCR analysis. A significant increase in TRPV1 mRNA expression occurred in TRG ipsilateral to CFA injected masseter muscle, whereas no significant alteration in TRPV1 occurred in the contralateral TRG. Interestingly, central injection of TRPV1 antagonist 5-iodoresiniferatoxin into the hippocampus significantly attenuated the head withdrawal response of both CFA injected and non-CFA injected contralateral masseter muscle. Our findings show that unilateral inflammation of masseter muscle is capable of inducing bilateral allodynia in rats. Upregulation of TRPV1 at the TRG level is due to nociception caused by inflammation, whereas contralateral nocifensive behavior in masticatory muscle nociception is likely mediated by central TRPV1, pointing to the involvement of altered information processing in higher centers. BioMed Central 2013-12-30 /pmc/articles/PMC3880456/ /pubmed/24377488 http://dx.doi.org/10.1186/1744-8069-9-68 Text en Copyright © 2013 Simonic-Kocijan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Simonic-Kocijan, Suncana
Zhao, Xuehong
Liu, Wen
Wu, Yuwei
Uhac, Ivone
Wang, KeWei
TRPV1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats
title TRPV1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats
title_full TRPV1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats
title_fullStr TRPV1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats
title_full_unstemmed TRPV1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats
title_short TRPV1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats
title_sort trpv1 channel-mediated bilateral allodynia induced by unilateral masseter muscle inflammation in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880456/
https://www.ncbi.nlm.nih.gov/pubmed/24377488
http://dx.doi.org/10.1186/1744-8069-9-68
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