PERIPHERAL P2X7 RECEPTOR-INDUCED MECHANICAL HYPERALGESIA IS MEDIATED BY BRADYKININ

被引:18
作者
Teixeira, J. M. [1 ]
de Oliveira-Fusaro, M. C. G. [2 ]
Parada, C. A. [1 ]
Tambeli, C. H. [1 ]
机构
[1] State Univ Campinas UNICAMP, Inst Biol, Dept Struct & Funct Biol, BR-13083862 Campinas, SP, Brazil
[2] State Univ Campinas UNICAMP, Fac Sci Appl, BR-13484350 Limeira, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
P2X7; receptor; BzATP; mechanical hyperalgesia; inflammatory mediators; pro-inflammatory cytokines; TUMOR-NECROSIS-FACTOR; INDUCED INFLAMMATORY HYPERALGESIA; P2X(7) RECEPTOR; EXTRACELLULAR ATP; MICROGLIAL CELLS; FACTOR-ALPHA; NEUROPATHIC PAIN; OXIDIZED ATP; TEMPOROMANDIBULAR-JOINT; IL-1-BETA RELEASE;
D O I
10.1016/j.neuroscience.2014.06.057
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
P2X7 receptors play an important role in inflammatory hyperalgesia, but the mechanisms involved in their hyperalgesic role are not completely understood. In this study, we hypothesized that P2X7 receptor activation induces mechanical hyperalgesia via the inflammatory mediators bradykinin, sympathomimetic amines, prostaglandin E-2 (PGE(2)), and pro-inflammatory cytokines and via neutrophil migration in rats. We found that 2'(3')-O-(4-benzoylbenzoyl)adenosine 5'-triphosphate triethylammonium salt (BzATP), the most potent P2X7 receptor agonist available, induced a dose-dependent mechanical hyperalgesia that was blocked by the P2X7 receptor-selective antagonist A-438079 but unaffected by the P2X1,3,2/3 receptor antagonist TNP-ATP. These findings confirm that, although BzATP also acts at both P2X1 and P2X3 receptors, BzATP-induced hyperalgesia was mediated only by P2X7 receptor activation. Co-administration of selective antagonists of bradykinin B-1 (Des-Arg(8)-Leu(9)-BK (DALBK)) or B-2 receptors (bradyzide), beta(1) (atenolol) or beta(2) adrenoceptors (ICI 118,551), or local pre-treatment with the cyclooxygenase inhibitor indomethacin or the nonspecific selectin inhibitor fucoidan each significantly reduced BzATP-induced mechanical hyperalgesia in the rat hind paw. BzATP also induced the release of the pro-inflammatory cytokines tumor necrosis factor alpha (TNF-alpha), interleukin (IL)-1 beta, IL-6 and cytokine-induced neutrophil chemoattractant-1 (CINC-1), an effect that was significantly reduced by A-438079. Co-administration of DALBK or bradyzide with BzATP significantly reduced BzATP-induced IL-1 beta and CINC-1 release. These results indicate that peripheral P2X7 receptor activation induces mechanical hyperalgesia via inflammatory mediators, especially bradykinin, which may contribute to pro-inflammatory cytokine release. These pro-inflammatory cytokines in turn may mediate the contributions of PGE(2), sympathomimetic amines and neutrophil migration to the mechanical hyperalgesia induced by local P2X7 receptor activation. (C) 2014 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:163 / 173
页数:11
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