Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/199036
Type: Artigo de periódico
Title: P2x3 And P2x2/3 Receptors Mediate Mechanical Hyperalgesia Induced By Bradykinin, But Not By Pro-inflammatory Cytokines, Pge₂ Or Dopamine.
Author: de Oliveira Fusaro, Maria Cláudia Gonçalves
Pelegrini-da-Silva, Adriana
Araldi, Dionéia
Parada, Carlos Amílcar
Tambeli, Cláudia Herrera
Abstract: Activation of peripheral P2X3 and P2X2/3 receptors by endogenous ATP is essential to the development of inflammatory hyperalgesia. We have previously demonstrated that this essential role of P2X3 and P2X2/3 receptors in the development of mechanical hyperalgesia induced by the inflammatory agent carrageenan is mediated by an indirect sensitization of the primary afferent nociceptors dependent on the previous release of tumor necrosis factor alpha (TNF-α) and by a direct sensitization of the primary afferent nociceptors. Therefore, in this study we asked whether activation of P2X3 and P2X2/3 receptors contribute to the mechanical hyperalgesia induced by the inflammatory mediators involved in carrageenan-induced mechanical hyperalgesia, such as bradykinin, tumor necrosis factor alpha (TNF-α), interleukin-1 beta (IL-1β), interleukin-6 (IL-6), chemokine-induced chemoattractant-1 (CINC-1), prostaglandin E₂ (PGE₂) and dopamine. Co-administration of the non-selective P2X3 receptor antagonist TNP-ATP or the selective P2X3 and P2X2/3 receptor antagonist A-317491 with bradykinin, but not with TNF-α, IL-1β, IL-6, CINC-1, PGE₂ or dopamine, prevented in a dose-dependent manner the mechanical hyperalgesia. We also verified whether the activation of P2X3 and P2X2/3 receptors by endogenous ATP contributes to bradykinin-induced mechanical hyperalgesia via neutrophil migration and/or cytokine release. Co-administration of TNP-ATP or A-317491 did not affect either neutrophil migration or the increased concentration of TNF-α, IL-1β, IL-6 and CINC-1 induced by bradykinin. These findings demonstrate that the activation of P2X3 and P2X2/3 receptors by endogenous ATP mediates bradykinin-induced mechanical hyperalgesia by a mechanism that does not depend on neutrophil migration or cytokines release.
Subject: Adenosine Triphosphate
Animals
Bradykinin
Cell Movement
Cytokines
Dinoprostone
Dopamine
Hyperalgesia
Inflammation
Inflammation Mediators
Male
Nerve Tissue Proteins
Neurons
Neutrophils
Pain Measurement
Purinergic P2x Receptor Antagonists
Rats
Rats, Wistar
Receptors, Purinergic P2x2
Receptors, Purinergic P2x3
Subcutaneous Tissue
Synaptic Transmission
Rights: fechado
Identifier DOI: 10.1016/j.ejphar.2010.09.037
Address: http://www.ncbi.nlm.nih.gov/pubmed/20868656
Date Issue: 2010
Appears in Collections:Unicamp - Artigos e Outros Documentos

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