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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/129711
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dc.contributor.authorMartinho, Frederico Canato-
dc.contributor.authorNascimento, Gustavo G.-
dc.contributor.authorLeite, Fabio R. M.-
dc.contributor.authorGomes, Ana P. M.-
dc.contributor.authorFreitas, Lilian F.-
dc.contributor.authorCamoes, Izabel C. G.-
dc.date.accessioned2015-10-22T06:35:14Z-
dc.date.accessioned2016-10-25T21:16:10Z-
dc.date.available2015-10-22T06:35:14Z-
dc.date.available2016-10-25T21:16:10Z-
dc.date.issued2015-02-01-
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0099239914009340-
dc.identifier.citationJournal Of Endodontics. New York: Elsevier Science Inc, v. 41, n. 2, p. 169-175, 2015.-
dc.identifier.issn0099-2399-
dc.identifier.urihttp://hdl.handle.net/11449/129711-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/129711-
dc.description.abstractIntroduction: This clinical study assessed the influence of different intracanal medications on Th1-type and Th2-type cytokine responses in apical periodontitis and monitored the levels of bacteria from primarily infection during endodontic procedures. Methods: Thirty primarily infected teeth were randomly divided into 3 groups according to the medication selected: chlorhexidine (CHX), 2% CHX gel; Ca(OH)2/SSL, Ca(OH)2 + SSL; and Ca(OH)2/CHX, Ca(OH)2 + 2% CHX gel (all, n = 10). Bacterial sample was collected from root canals, and the interstitial fluid was sampled from lesions. Culture techniques were used to determine bacterial counts (colony-forming units/mL). Th1 (tumor necrosis factor-a, interferon-gamma, and interleukin [IL]-2) and Th2 cytokines (IL-4, IL-5, and IL-13) were measured by enzyme-linked immunosorbent assay. Results: All intracanal medication protocols were effective in reducing the bacterial load from root canals (all P < .05) and lowering the levels of Th1-type cytokines in apical lesions (all P < .05), with no differences between them (P > .05). Both Ca(OH)2 treatment protocols significantly increased the levels of Th2-type cytokines (P < .05), with no differences between them (P > .05). Thus, chlorhexidine medication showed the lowest effectiveness in increasing the levels of Th2-type cytokine. After treatment, regardless of the type of medication, the linear regression analysis indicated the down-regulation of Th2-type cytokines by Th1-type cytokines. Conclusions: All intracanal medication protocols were effective in reducing bacterial load and lowering the levels of Th1-type cytokines. Thus, the use of Ca(OH)2 medications contributed to the increase in the Th2-type cytokine response in apical periodontitis.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent169-175-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectDisinfectionen
dc.subjectendodonticsen
dc.subjectmedicationen
dc.subjectroot canalen
dc.titleClinical Influence of Different Intracanal Medications on Th1-type and Th2-type Cytokine Responses in Apical Periodontitisen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniv Fed Pelotas-
dc.contributor.institutionUniversidade Federal Fluminense (UFF)-
dc.description.affiliationUNESP UNIV Estadual Paulista, Endodont Div, Dept Restorat Dent, Sao Paulo, Brazil-
dc.description.affiliationState Univ Campinas UNICAMP, Endodont Div, Dept Restorat Dent, Piracicaba Dent Sch, Sao Paulo, Brazil-
dc.description.affiliationUniv Fed Pelotas, Sch Dent, Dept Semiol &Clin, Periodont Div, Pelotas, RS, Brazil-
dc.description.affiliationFluminense Fed Univ UFF, Dept Restorat Dent, Endodont Div, Niteroi, RJ, Brazil-
dc.description.affiliationUnespUNESP UNIV Estadual Paulista, Endodont Div, Dept Restorat Dent, Sao Paulo, Brazil-
dc.description.sponsorshipIdFAPESP: 2012/19536-5-
dc.description.sponsorshipIdFAPESP: 2013/04354-1-
dc.description.sponsorshipIdCNPq: 23038009469/2012-24-
dc.identifier.doihttp://dx.doi.org/10.1016/j.joen.2014.09.028-
dc.identifier.wosWOS:000349424300006-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal Of Endodontics-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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