Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/34905
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dc.contributor.authorDenadai-Souza, Alexandre [UNIFESP]
dc.contributor.authorMartin, Laurence
dc.contributor.authorPaula, Marco A. Vieira de
dc.contributor.authorAvellar, Maria Christina Werneck [UNIFESP]
dc.contributor.authorMuscara, Marcelo N.
dc.contributor.authorVergnolle, Nathalie
dc.contributor.authorCenac, Nicolas
dc.date.accessioned2016-01-24T14:27:15Z-
dc.date.available2016-01-24T14:27:15Z-
dc.date.issued2012-06-01
dc.identifierhttp://dx.doi.org/10.1002/art.34345
dc.identifier.citationArthritis and Rheumatism. Hoboken: Wiley-Blackwell, v. 64, n. 6, p. 1848-1858, 2012.
dc.identifier.issn0004-3591
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/34905-
dc.description.abstractObjective To determine whether activation of transient receptor potential vanilloid 4 (TRPV-4) induces inflammation in the rat temporomandibular joint (TMJ), and to assess the effects of TRPV-4 agonists and proinflammatory mediators, such as a protease-activated receptor 2 (PAR-2) agonist, on TRPV-4 responses. Methods Four hours after intraarticular injection of carrageenan into the rat joints, expression of TRPV-4 and PAR-2 in trigeminal ganglion (TG) neurons and in the TMJs were evaluated by real-time reverse transcriptionpolymerase chain reaction and immunofluorescence, followed by confocal microscopy. the functionality of TRPV-4 and its sensitization by a PAR-2activating peptide (PAR-2AP) were analyzed by measuring the intracellular Ca2+ concentration in TMJ fibroblast-like synovial cells or TG neurons. Plasma extravasation, myeloperoxidase activity, and the head-withdrawal threshold (index of mechanical allodynia) were evaluated after intraarticular injection of selective TRPV-4 agonists, either injected alone or coinjected with PAR-2AP. Results in the rat TMJs, TRPV-4 and PAR-2 expression levels were up-regulated after the induction of inflammation. Two TRPV-4 agonists specifically activated calcium influx in TMJ fibroblast-like synovial cells or TG neurons. in vivo, the agonists triggered dose-dependent increases in plasma extravasation, myeloperoxidase activity, and mechanical allodynia. in synovial cells or TG neurons, pretreatment with PAR-2AP potentiated a TRPV-4 agonistinduced increase in [Ca2+]i. in addition, TRPV-4 agonistinduced inflammation was potentiated by PAR-2AP in vivo. Conclusion in this rat model, TRPV-4 is expressed and functional in TG neurons and synovial cells, and activation of TRPV-4 in vivo causes inflammation in the TMJ. Proinflammatory mediators, such as PAR-2 agonists, sensitize the activity of TRPV-4. These results identify TRPV-4 as an important signal of inflammation in the joint.en
dc.description.sponsorshipINSERM-Avenir
dc.description.sponsorshipBettencourt-Schueller Foundation
dc.description.sponsorshipFoundation for Medical Research
dc.description.sponsorshipAgence Nationale de la Recherche
dc.description.sponsorshipCanadian Institute of Health Research
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.format.extent1848-1858
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofArthritis and Rheumatism
dc.rightsAcesso aberto
dc.titleRole of transient receptor potential vanilloid 4 in rat joint inflammationen
dc.typeArtigo
dc.rights.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUniv Toulouse 3
dc.contributor.institutionCNRS
dc.contributor.institutionUniv Calgary
dc.description.affiliationUniv São Paulo, São Paulo, Brazil
dc.description.affiliationUniversidade Federal de São Paulo, São Paulo, Brazil
dc.description.affiliationUniv Toulouse 3, Ctr Physiopathol Toulouse Purpan, INSERM, U1043, F-31062 Toulouse, France
dc.description.affiliationCNRS, U5282, Toulouse, France
dc.description.affiliationUniv Calgary, Calgary, AB, Canada
dc.description.affiliationUnifespUniversidade Federal de São Paulo, São Paulo, Brazil
dc.description.sponsorshipIDFAPESP: 2009/12375-3
dc.identifier.doi10.1002/art.34345
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000304522100018
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