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      Journal of Pain Research (submit here)

      This international, peer-reviewed Open Access journal by Dove Medical Press focuses on reporting of high-quality laboratory and clinical findings in all fields of pain research and the prevention and management of pain. Sign up for email alerts here.

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      Is Open Access

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

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          Abstract

          Purpose

          P 2Y 2 receptors (P 2Y 2Rs) are among the various receptors that play an important role in nociception. The goal of this research was to investigate possible P 2Y 2R 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 2Y 2R 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 2Y 2Rs in nocifensive behavior was evaluated by administering two doses of P 2Y 2R 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 2Y 2R 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 2Y 2Rs may affect MM inflammatory hypersensitivity owing to its up-regulation in the TRG in MM inflammatory pain states.

          Most cited references34

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          Mechanisms of release of nucleotides and integration of their action as P2X- and P2Y-receptor activating molecules.

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            Contribution of the activation of satellite glia in sensory ganglia to pathological pain.

            Peripheral tissue injury/inflammation can alter the properties of somatic sensory pathways, resulting in behavioral hypersensitivity and pathological and/or chronic pain, including increased responses to pain caused by both noxious stimuli (hyperalgesia) and normally innocuous stimuli (allodynia). Although there are increasing reports that glia in the spinal cord contribute to the maintenance of pathological pain, recent evidence suggests that activation of satellite glia in sensory ganglia may also play an important role in the development of hyperalgesia and allodynia. There is evidence that non-synaptically released chemical mediators derived from both neurons and satellite glia may trigger chronic pain via autocrine and/or paracrine mechanisms and that augmented excitability of primary afferent neurons results in changes in central pain-signaling neurons (central sensitization). The focus of the present review is on the contribution of the activation of satellite glia in sensory ganglia to pathological pain. In addition, we discuss potential therapeutic targets in satellite glia-neuronal interactions for the prevention of pathological pain.
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              Peripheral and central mechanisms of orofacial inflammatory pain.

              Many orofacial pain conditions involve inflammation of orofacial tissues and they range from acute pulpitis (toothache) and mucositis to chronic arthritic conditions affecting the temporomandibular joint (TMJ). This article reviews the peripheral and central neural mechanisms involved in orofacial inflammatory pain states, including the integral role that peripheral and central sensitization play in the pain features that characterize these states. It also outlines the recent evidence for the contribution of non-neural processes, especially those involving glial cells. Copyright © 2011 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                J Pain Res
                J Pain Res
                JPR
                jpainres
                Journal of Pain Research
                Dove
                1178-7090
                03 June 2020
                2020
                : 13
                : 1323-1333
                Affiliations
                [1 ]Department of Prosthodontics, Faculty of Dental Medicine, University of Rijeka , Rijeka, Croatia
                [2 ]Department of Prosthodontics, Clinic of Dental Medicine, Clinical Hospital Center Rijeka , Rijeka, Croatia
                [3 ]Department of Orthodontics, Clinic of Dental Medicine, Clinical Hospital Center Rijeka , Rijeka, Croatia
                [4 ]Department of Removable Prosthodontics, School of Dental Medicine, University of Zagreb , Zagreb, Croatia
                Author notes
                Correspondence: Sunčana Simonić-Kocijan Department of Prosthodontics, Faculty of Dental Medicine, University of Rijeka , Krešimirova 40, Rijeka51000, CroatiaTel +385 51 345 633Fax +385 51 345 630 Email suncanask@uniri.hr
                Author information
                http://orcid.org/0000-0001-6333-8533
                http://orcid.org/0000-0002-0671-9820
                http://orcid.org/0000-0002-1360-3279
                http://orcid.org/0000-0002-8117-9203
                http://orcid.org/0000-0002-8323-6515
                Article
                239831
                10.2147/JPR.S239831
                7280063
                ebacb2c1-2771-4ec3-ba28-9b5713f7c97b
                © 2020 Tariba Knežević et al.

                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).

                History
                : 24 November 2019
                : 07 May 2020
                Page count
                Figures: 5, References: 38, Pages: 11
                Funding
                Funded by: University of Rijeka, Croatia
                This study was part of the project “Ethiopathogenesis of Orofacial Pain” at the University of Rijeka, Croatia and was funded within it.
                Categories
                Original Research

                Anesthesiology & Pain management
                facial pain,masticatory muscles,temporomandibular disorders,trigeminal ganglion

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