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P(2)Y(2) Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats

PURPOSE: P(2)Y(2) receptors (P(2)Y(2)Rs) are among the various receptors that play an important role in nociception. The goal of this research was to investigate possible P(2)Y(2)R expression changes in the trigeminal ganglion (TRG) in bilateral masseter muscle (MM) hypersensitivity following unilat...

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Autores principales: Tariba Knežević, Petra, Vukman, Robert, Uhač, Mia, Illeš, Davor, Kovačević Pavičić, Daniela, Simonić-Kocijan, Sunčana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280063/
https://www.ncbi.nlm.nih.gov/pubmed/32581574
http://dx.doi.org/10.2147/JPR.S239831
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author Tariba Knežević, Petra
Vukman, Robert
Uhač, Mia
Illeš, Davor
Kovačević Pavičić, Daniela
Simonić-Kocijan, Sunčana
author_facet Tariba Knežević, Petra
Vukman, Robert
Uhač, Mia
Illeš, Davor
Kovačević Pavičić, Daniela
Simonić-Kocijan, Sunčana
author_sort Tariba Knežević, Petra
collection PubMed
description PURPOSE: P(2)Y(2) receptors (P(2)Y(2)Rs) are among the various receptors that play an important role in nociception. The goal of this research was to investigate possible P(2)Y(2)R expression changes in the trigeminal ganglion (TRG) in bilateral masseter muscle (MM) hypersensitivity following unilateral MM inflammation. The impact of unilateral intramasseteric administration of P(2)Y(2)R antagonist on bilateral MM hypersensitivity was also explored. MATERIALS AND METHODS: Bilateral MM hypersensitivity was provoked by unilateral intramasseteric injection of complete Freund’s adjuvant (CFA). The head withdrawal threshold (HWT) was assessed bilaterally 4 days later. Bilateral TRG and MM isolation were followed, and quantitative real-time polymerase chain reaction (qRT-PCR) and histopathological analysis were carried out on these tissues, respectively. The involvement of P(2)Y(2)Rs in nocifensive behavior was evaluated by administering two doses of P(2)Y(2)R antagonist AR-C118925 (0.2 or 1 mg/100 μL) in inflamed MM 4 days post-CFA administration. Bilateral HWT was assessed at different time points following antagonist injection. RESULTS: qRT-PCR analysis demonstrated P(2)Y(2)R up-regulation in TRG ipsilateral to the site of CFA administration. Compared to the controls, both doses of AR-C118925 injected ipsilateral to the TRG increased the bilateral HWT at 30, 60, 90, and 120 minutes after antagonist administration. CONCLUSION: The findings suggest that P(2)Y(2)Rs may affect MM inflammatory hypersensitivity owing to its up-regulation in the TRG in MM inflammatory pain states.
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spelling pubmed-72800632020-06-23 P(2)Y(2) Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats Tariba Knežević, Petra Vukman, Robert Uhač, Mia Illeš, Davor Kovačević Pavičić, Daniela Simonić-Kocijan, Sunčana J Pain Res Original Research PURPOSE: P(2)Y(2) receptors (P(2)Y(2)Rs) are among the various receptors that play an important role in nociception. The goal of this research was to investigate possible P(2)Y(2)R expression changes in the trigeminal ganglion (TRG) in bilateral masseter muscle (MM) hypersensitivity following unilateral MM inflammation. The impact of unilateral intramasseteric administration of P(2)Y(2)R antagonist on bilateral MM hypersensitivity was also explored. MATERIALS AND METHODS: Bilateral MM hypersensitivity was provoked by unilateral intramasseteric injection of complete Freund’s adjuvant (CFA). The head withdrawal threshold (HWT) was assessed bilaterally 4 days later. Bilateral TRG and MM isolation were followed, and quantitative real-time polymerase chain reaction (qRT-PCR) and histopathological analysis were carried out on these tissues, respectively. The involvement of P(2)Y(2)Rs in nocifensive behavior was evaluated by administering two doses of P(2)Y(2)R antagonist AR-C118925 (0.2 or 1 mg/100 μL) in inflamed MM 4 days post-CFA administration. Bilateral HWT was assessed at different time points following antagonist injection. RESULTS: qRT-PCR analysis demonstrated P(2)Y(2)R up-regulation in TRG ipsilateral to the site of CFA administration. Compared to the controls, both doses of AR-C118925 injected ipsilateral to the TRG increased the bilateral HWT at 30, 60, 90, and 120 minutes after antagonist administration. CONCLUSION: The findings suggest that P(2)Y(2)Rs may affect MM inflammatory hypersensitivity owing to its up-regulation in the TRG in MM inflammatory pain states. Dove 2020-06-03 /pmc/articles/PMC7280063/ /pubmed/32581574 http://dx.doi.org/10.2147/JPR.S239831 Text en © 2020 Tariba Knežević et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Tariba Knežević, Petra
Vukman, Robert
Uhač, Mia
Illeš, Davor
Kovačević Pavičić, Daniela
Simonić-Kocijan, Sunčana
P(2)Y(2) Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats
title P(2)Y(2) Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats
title_full P(2)Y(2) Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats
title_fullStr P(2)Y(2) Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats
title_full_unstemmed P(2)Y(2) Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats
title_short P(2)Y(2) Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats
title_sort p(2)y(2) receptors mediate masseter muscle mechanical hypersensitivity in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280063/
https://www.ncbi.nlm.nih.gov/pubmed/32581574
http://dx.doi.org/10.2147/JPR.S239831
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