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Evaluation of photodynamic therapy on fibroblast viability and cytokine production

dc.contributor.authorGomes-Filho, Joao Eduardo [UNESP]
dc.contributor.authorSivieri-Araujo, Gustavo [UNESP]
dc.contributor.authorSipert, Carla Renata
dc.contributor.authorSilva Santos, Ludmilla Mota da [UNESP]
dc.contributor.authorAzevedo Queiroz, India Olinta de [UNESP]
dc.contributor.authorMartins, Christine Men [UNESP]
dc.contributor.authorCarmo Maia, Nayara Kivilla do [UNESP]
dc.contributor.authorAngelo Cintra, Luciano Tavares [UNESP]
dc.contributor.authorDezan-Junior, Eloi [UNESP]
dc.contributor.authorBagnato, Vanderlei Salvador
dc.contributor.authorChaves-Neto, Antonio Hernandes [UNESP]
dc.contributor.authorPenha de Oliveira, Sandra Helena [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2018-11-26T16:28:05Z
dc.date.available2018-11-26T16:28:05Z
dc.date.issued2016-03-01
dc.description.abstractBackground: The aim of this study was to evaluate the effects of photodynamic therapy with curcumin (PDT) comparatively to 5% sodium hypochlorite (NaOCl) and saline solution on cell viability and cytokine (IL-1 beta and IL-6) production by mouse fibroblasts. Methods: Sixty seconds of pre-irradiation time with curcumin 500 mg/L and Led wavelength (lambda) 480 nm, 72 J cm(2), for 300 s was used for PDT. Solutions were diluted in culture medium DMEM (1 x 10(4) cells) and placed into 24-well cell culture plates with mouse fibroblasts L-929. Culture medium was used as control. After 6,24 and 48 h, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay (MIT) was used to evaluate the cell viability and the supernatant was collected for cytokine evaluation using enzyme-linked immunosorbent assay (ELISA). The results were statistically analyzed by ANOVA and BonFerroni correction (p < 0.05) for MIT and Kruskal-Wallis test and Dunn (p < 0.05) for ELISA. Results: PDT and saline solution presented low cytotoxic effect similar to the control group (p > 0.05) while 5% NaOCl was more cytotoxic than PDT (p < 0.05) in all periods of time. All materials similarly expressed IL-1 beta and IL-6 regardless to the experimental period (p < 0.05). Conclusions: PDT with curcumin was not cytotoxic to L929 fibroblasts differently from 5% NaOCl. In all groups occurred similar expression of IL-1 beta and IL-6. (C) 2016 Elsevier B.V. All rights reserved.en
dc.description.affiliationSao Paulo State Univ, Aracatuba Sch Dent, Discipline Endodont, Dept Restorat Dent, Aracatuba, SP, Brazil
dc.description.affiliationUniv Sao Paulo, Sch Dent, Discipline Endodont, Dept Restorat Dent, Sao Paulo, SP, Brazil
dc.description.affiliationUniv Sao Paulo, Phys Inst Sao Carlos, Opt Grp, Sao Carlos, SP, Brazil
dc.description.affiliationSao Paulo State Univ, Aracatuba Sch Dent, Discipline Biochem, Dept Basic Sci, Aracatuba, SP, Brazil
dc.description.affiliationSao Paulo State Univ, Aracatuba Sch Dent, Discipline Pharmacol, Dept Basic Sci, Aracatuba, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Aracatuba Sch Dent, Discipline Endodont, Dept Restorat Dent, Aracatuba, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Aracatuba Sch Dent, Discipline Biochem, Dept Basic Sci, Aracatuba, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Aracatuba Sch Dent, Discipline Pharmacol, Dept Basic Sci, Aracatuba, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2011/23287-8
dc.description.sponsorshipIdFAPESP: 2012/12695-0
dc.description.sponsorshipIdFAPESP: 2012/06785-7
dc.format.extent97-100
dc.identifierhttp://dx.doi.org/10.1016/j.pdpdt.2016.01.007
dc.identifier.citationPhotodiagnosis And Photodynamic Therapy. Amsterdam: Elsevier Science Bv, v. 13, p. 97-100, 2016.
dc.identifier.doi10.1016/j.pdpdt.2016.01.007
dc.identifier.fileWOS000372376500015.pdf
dc.identifier.issn1572-1000
dc.identifier.urihttp://hdl.handle.net/11449/161333
dc.identifier.wosWOS:000372376500015
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofPhotodiagnosis And Photodynamic Therapy
dc.relation.ispartofsjr0,647
dc.rights.accessRightsAcesso abertopt
dc.sourceWeb of Science
dc.subjectEndodontic treatment
dc.subjectRoot canal irrigants
dc.subjectPhotodynamic therapy
dc.subjectCytotoxicity
dc.subjectCytokine
dc.titleEvaluation of photodynamic therapy on fibroblast viability and cytokine productionen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.author.lattes1743697225702984[11]
unesp.author.orcid0000-0002-8402-7408[2]
unesp.author.orcid0000-0001-6452-6990[7]
unesp.author.orcid0000-0001-6481-5506[11]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.departmentCiências Básicas - FOApt
unesp.departmentOdontologia Restauradora - FOApt

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