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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/14961
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dc.contributor.authorKanno, Claudia M.-
dc.contributor.authorOliveira, José Américo de-
dc.contributor.authorGarcia, José Fernando-
dc.contributor.authorCastro, Alvimar Lima de-
dc.contributor.authorCrivelini, Marcelo Macedo-
dc.date.accessioned2013-09-30T18:29:09Z-
dc.date.accessioned2014-05-20T13:43:00Z-
dc.date.accessioned2016-10-25T16:57:40Z-
dc.date.available2013-09-30T18:29:09Z-
dc.date.available2014-05-20T13:43:00Z-
dc.date.available2016-10-25T16:57:40Z-
dc.date.issued2008-01-01-
dc.identifierhttp://dx.doi.org/10.1902/jop.2008.070267-
dc.identifier.citationJournal of Periodontology. Chicago: Amer Acad Periodontology, v. 79, n. 1, p. 114-122, 2008.-
dc.identifier.issn0022-3492-
dc.identifier.urihttp://hdl.handle.net/11449/14961-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/14961-
dc.description.abstractBackground: The purpose of this experimental study was to evaluate the collagen fiber distribution histologically after phenytoin, cyclosporin, or nifedipine therapy and to correlate it with collagen I and matrix metalloproteinase (MMP)-1 and -2 gene expression levels.Methods: Gingival samples from the canine area were obtained from 12 male monkeys (Cebus apella). The mesial part of each sample was assessed by reverse transcription-polymerase chain reaction, whereas the distal part was processed histologically for picrosirius red and hematoxylin and eosin stainings, as well as for collagen IV immunostaining. One week after the first biopsy, the animals were assigned to three groups that received daily oral dosages of cyclosporin, phenytoin, or nifedipine for 120 days. Additional gingival samples were obtained on days 52 and 120 of treatment from two animals from each group on the opposite sides from the first biopsies.Results: Picrosirius red staining showed a predominance of mature collagen fibers in the control group. Conversely, there was an enlargement of areas occupied by immature collagen fibers in all groups at days 52 and 120, which was not uniform over each section. There was a general trend to lower levels of MMP-1 gene expression on day 52 and increased levels on day 120. Phenytoin led to increased levels of MMP-2 and collagen I gene expression on day 120, whereas the opposite was observed in the nifedipine group.Conclusion: Cyclosporin, phenytoin, and nifedipine led to phased and drug-related gene expression patterns, resulting in impaired collagen metabolism, despite the lack of prominent clinical signs.en
dc.format.extent114-122-
dc.language.isoeng-
dc.publisherAmer Acad Periodontology-
dc.sourceWeb of Science-
dc.subjectcollagen type Ien
dc.subjectcyclosporinen
dc.subjectgingival overgrowth/chemically induceden
dc.subjectmatrix metalloproteinaseen
dc.subjectnifedipineen
dc.subjectphenytoinen
dc.titleEffects of cyclosporin, phenytoin, and nifedipine on the synthesis and degradation of gingival collagen in tufted capuchin monkeys (Cebus apella): Histochemical and MMP-1 and -2 and collagen I gene expression analysesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationSão Paulo State Univ, Sch Dent, Postgrad Program, BR-16015050 Aracatuba, SP, Brazil-
dc.description.affiliationSão Paulo State Univ, Sch Dent, Dept Basic Sci, BR-16015050 Aracatuba, SP, Brazil-
dc.description.affiliationSão Paulo State Univ, Sch Dent, Sch Vet Med, Dept Anim Prod & Hlth, BR-16015050 Aracatuba, SP, Brazil-
dc.description.affiliationSão Paulo State Univ, Sch Dent, Dept Oral Pathol, BR-16015050 Aracatuba, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Sch Dent, Postgrad Program, BR-16015050 Aracatuba, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Sch Dent, Dept Basic Sci, BR-16015050 Aracatuba, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Sch Dent, Sch Vet Med, Dept Anim Prod & Hlth, BR-16015050 Aracatuba, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Sch Dent, Dept Oral Pathol, BR-16015050 Aracatuba, SP, Brazil-
dc.identifier.doi10.1902/jop.2008.070267-
dc.identifier.wosWOS:000252256100015-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Periodontology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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