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P2X7 受体诱导的大鼠颞下颌关节疼痛依赖于炎症机制和 C 纤维敏化。

P2X7-induced nociception in the temporomandibular joint of rats depends on inflammatory mechanisms and C-fibres sensitization.

机构信息

Faculdade São Leopoldo Mandic, Área de Fisiologia, Instituto de Pesquisas São Leopoldo Mandic, Campinas, Brazil.

Laboratory of Orofacial Pain, Department of Physiology, Piracicaba Dental School, State University of Campinas (UNICAMP), Piracicaba, Brazil.

出版信息

Eur J Pain. 2021 May;25(5):1107-1118. doi: 10.1002/ejp.1732. Epub 2021 Feb 5.

Abstract

BACKGROUND

P2X7 receptors are responsible for triggering inflammatory responses contributing to processes of pain in articular tissues. This study aimed to investigate whether the activation of the P2X7 receptor located in the temporomandibular joint (TMJ) tissues induces nociception through an inflammatory mechanisms and/or the activation of C-fibres (small-diameter primary afferents) of rats' TMJ.

METHODS

The TMJ hypernociception induced by the activation of P2X7 receptor was assessed by measuring the behavioural nociceptive responses. After behavioural experiments, the animals were terminally anaesthetized and periarticular tissues were removed and homogenate for enzyme-linked immunosorbent assay, leukocyte infiltration and western blotting analysis.

RESULTS

The nonselective P2X7 receptor agonist BzATP induced a dose-dependent TMJ nociception, which was blocked by the selective P2X7 receptor antagonist A-438079. The co-administration of the selective β2-adrenoceptor antagonist (ICI-118,551) and the pre-treatment with cyclooxygenase inhibitor indomethacin or with the nonspecific selectin inhibitor Fucoidan significantly reduced BzATP-induced TMJ nociception. BzATP also induced an increase of pro-inflammatory cytokines TNFα, IL-1β and CINC-1 levels, as well as leukocyte recruitment in TMJ tissue, effects that were reduced by A-438079. Moreover BzATP-induced TMJ nociception was inhibited in rats neonatal-treated with Capsaicin (depleting C-fibers). Finally, BzATP-induced an increase in TRPV1 expression in TMJ tissue.

CONCLUSIONS

These findings suggest that P2X7 receptor activation in TMJ of rats induces nociceptive responses mediated by sympathomimetic amines, prostaglandins, leukocyte migration and increased levels of pro-inflammatory cytokines. Furthermore, the P2X7 receptor activation induces nociceptive responses dependent on the activation of the primary afferent nociceptors of rats' TMJ.

SIGNIFICANCE

The activation of P2X7 receptors has an essential role in TMJ nociception and could be an interesting target to control the inflammatory pain in temporomandibular disorders.

摘要

背景

P2X7 受体负责触发炎症反应,从而导致关节组织疼痛过程。本研究旨在探讨位于颞下颌关节(TMJ)组织中的 P2X7 受体的激活是否通过炎症机制和/或 TMJ 大鼠 C 纤维(小直径初级传入纤维)的激活来诱导伤害感受。

方法

通过测量行为性疼痛反应来评估 P2X7 受体激活引起的 TMJ 超敏反应。行为实验后,麻醉处死动物,取出关节周围组织,进行酶联免疫吸附试验、白细胞浸润和 Western blot 分析。

结果

非选择性 P2X7 受体激动剂 BzATP 诱导剂量依赖性 TMJ 伤害感受,该感受可被选择性 P2X7 受体拮抗剂 A-438079 阻断。选择性β2-肾上腺素能受体拮抗剂(ICI-118,551)的共给药和环氧化酶抑制剂吲哚美辛或非特异性选择素抑制剂 Fucoidan 的预处理显著降低了 BzATP 诱导的 TMJ 伤害感受。BzATP 还诱导 TMJ 组织中促炎细胞因子 TNFα、IL-1β 和 CINC-1 水平的增加以及白细胞募集,这些作用可被 A-438079 减弱。此外,Capsaicin(耗尽 C 纤维)处理的新生大鼠的 BzATP 诱导的 TMJ 伤害感受受到抑制。最后,BzATP 诱导 TMJ 组织中 TRPV1 表达增加。

结论

这些发现表明,大鼠 TMJ 中 P2X7 受体的激活诱导伤害感受反应,该反应由拟交感胺、前列腺素、白细胞迁移和促炎细胞因子水平升高介导。此外,P2X7 受体的激活诱导伤害感受反应依赖于大鼠 TMJ 初级传入伤害感受器的激活。

意义

P2X7 受体的激活在 TMJ 伤害感受中起重要作用,可能是控制颞下颌关节紊乱炎症性疼痛的一个有趣靶点。

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