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Effect of selective cyclooxygenase-2 inhibition on the development of ligature-induced periodontitis in rats

dc.contributor.authorHolzhausen, M.
dc.contributor.authorRossa, C.
dc.contributor.authorMarcantonio, E.
dc.contributor.authorNassar, P. O.
dc.contributor.authorSpolidório, Denise Madalena Palomari [UNESP]
dc.contributor.authorSpolidório, Luis Carlos [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:45:45Z
dc.date.available2014-05-20T13:45:45Z
dc.date.issued2002-09-01
dc.description.abstractBackground: the purpose of this study was to evaluate the effect of a selective cyclooxygenase-2 inhibitor on the progression of alveolar bone loss in an experimental periodontitis model in rats.Methods: One hundred eighty (180) Wistar rats were separated into 3 experimental groups. Cotton ligatures were placed at the gingival margin level of lower right first molars. The rats were randomly assigned to one of the following groups that received: a daily oral dose of 10 mg/kg body weight of celecoxib (Ce1); 20 mg/kg body weight of celecoxib (Ce2); or 10 ml/kg of saline solution (C). Serum levels of celecoxib and white blood cell count were determined. Standardized digital radiographs were taken after sacrifice at 3, 5, 10, 18, and 30 days to measure the amount of bone loss around the mesial root surface of the first molar tooth in each rat.Results: Two-way analysis of variance (ANOVA) indicated that groups treated with celecoxib had significantly less bone loss compared to controls (P <0.0001) and that there was a significant interaction between treatment with celecoxib and time (P <0.03). Post-hoc comparisons showed that in both groups treated with celecoxib, the bone loss became significant only after 10 days of ligature placement, while in the control group it was already significant after 5 days. However, differences in mean bone loss between control and Ce1 were significant only at 18 days and, between control and Ce2, at 5 and 18 days. There was no significant difference in bone loss among experimental groups at the end of the experimental period.Conclusion: These data provide evidence that systemic therapy with celecoxib can modify the progression of experimentally induced periodontitis in rats.en
dc.description.affiliationUNESP, Fac Odontol Araraquara, Dept Patol Oral, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationState Univ São Paulo, Dept Periodontol, Araraquara Dent Sch, Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Odontol Araraquara, Dept Patol Oral, BR-14801903 Araraquara, SP, Brazil
dc.description.affiliationUnespState Univ São Paulo, Dept Periodontol, Araraquara Dent Sch, Araraquara, SP, Brazil
dc.format.extent1030-1036
dc.identifierhttp://dx.doi.org/10.1902/jop.2002.73.9.1030
dc.identifier.citationJournal of Periodontology. Chicago: Amer Acad Periodontology, v. 73, n. 9, p. 1030-1036, 2002.
dc.identifier.doi10.1902/jop.2002.73.9.1030
dc.identifier.issn0022-3492
dc.identifier.lattes2640929291808415
dc.identifier.urihttp://hdl.handle.net/11449/16121
dc.identifier.wosWOS:000178011800009
dc.language.isoeng
dc.publisherAmer Acad Periodontology
dc.relation.ispartofJournal of Periodontology
dc.relation.ispartofjcr3.392
dc.relation.ispartofsjr1,408
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectalveolar bone loss/prevention and controlpt
dc.subjectcyclooxygenase inhibitorspt
dc.subjectanimal studiespt
dc.subjectperiodontitis/prevention and controlpt
dc.titleEffect of selective cyclooxygenase-2 inhibition on the development of ligature-induced periodontitis in ratsen
dc.typeArtigopt
dcterms.licensehttp://www.joponline.org/userimages/ContentEditor/1124388816475/Instructions_to_Authors.pdf
dcterms.rightsHolderAmer Acad Periodontology
dspace.entity.typePublication
relation.isDepartmentOfPublicationb3ba3d9c-022e-4521-8805-0bcceea7372e
relation.isDepartmentOfPublication.latestForDiscoveryb3ba3d9c-022e-4521-8805-0bcceea7372e
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.author.lattes2640929291808415
unesp.author.lattes7634063102292261[2]
unesp.author.orcid0000-0003-2376-1024[5]
unesp.author.orcid0000-0003-1705-5481[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentDiagnóstico e Cirurgia - FOARpt
unesp.departmentFisiologia e Patologia - FOARpt

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