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http://hdl.handle.net/1843/45492
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DC Field | Value | Language |
---|---|---|
dc.creator | Francine Benetti | pt_BR |
dc.creator | André Luiz Fraga Briso | pt_BR |
dc.creator | Araújo Lopes | pt_BR |
dc.creator | Carminatti | pt_BR |
dc.creator | Conti | pt_BR |
dc.creator | Marjorie de Oliveira Gallinari | pt_BR |
dc.creator | Edilson Ervolino | pt_BR |
dc.creator | Luciano Tavares Angelo Cintra | pt_BR |
dc.date.accessioned | 2022-09-24T20:53:45Z | - |
dc.date.available | 2022-09-24T20:53:45Z | - |
dc.date.issued | 2019-07-19 | - |
dc.citation.volume | 52 | pt_BR |
dc.citation.issue | 12 | pt_BR |
dc.citation.spage | 1723 | pt_BR |
dc.citation.epage | 1737 | pt_BR |
dc.identifier.doi | https://doi.org/10.1111/iej.13190 | pt_BR |
dc.identifier.issn | 01432885 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/1843/45492 | - |
dc.description.resumo | AimTo investigate hydrogen peroxide (H2O2)-inducedresponsiveness in pulp cells using heme oxygenase-1(HO-1) immunolabelling, Jun-D immunolabelling tostudy the effects of H2O2on odontoblastic differentiationand CD90+/CD73+/CD105+/CD45 cell counting forin vivoidentification of mesenchymal stem cells in thepulp.MethodologyThe maxillary molars of 50 rats weretreated with a bleaching gel (35% H2O2,1930 min) orplacebo gel (control groups). At 2, 3, 7, 15 and 30 daysafter the treatment (n=10), inflammation in pulp tissuewas analysed by haematoxylin–eosin staining, HO-1-and Jun-D-immunolabelled cells were counted ineach third of the pulp chamber, and the number ofCD90+/CD73+/CD105+/CD45 cells was quantified byimmunofluorescence. The results were assessed using thePairedt-test or Wilcoxon signed-rank test (P<0.05).ResultsSignificant H2O2-induced inflammation wasnoted at 2 and 3 days (P<0.05), with tertiary den-tine formation occurring from 7 days. The bleachedspecimens had greater HO-1 immunolabelling in themiddle and cervical thirds of the coronal pulp at 2and 3 days, in all thirds at 7 days, and in the occlu-sal third at 15 days (P<0.05), and significantnuclear Jun-D immunolabelling in the cervical thirdat 2 and 3 days and in the occlusal and middle thirdsat 7 days (P<0.05). Bleached and control groupshad low numbers of CD90+/CD73+/CD105+/CD45 cells in the pulp at all periods (P>0.05).ConclusionsPulp cells responded to oxidative stressby expressing HO-1 during the post-bleaching inflam-mation phase until the beginning of the repair phase.Jun-D expression occurred during the reduction ofinflammation and the beginning of tertiary dentine production. The presence of oxidative stress did notinfluence the number of CD90+/CD73+/CD105+/CD45 cells identifiedin vivo in the dental pulp | pt_BR |
dc.description.sponsorship | CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico | pt_BR |
dc.description.sponsorship | FAPESP - Fundação de Amparo à Pesquisa do Estado de São Paulo | pt_BR |
dc.format.mimetype | pt_BR | |
dc.language | eng | pt_BR |
dc.publisher | Universidade Federal de Minas Gerais | pt_BR |
dc.publisher.country | Brasil | pt_BR |
dc.publisher.department | FAO - DEPARTAMENTO DE ODONTOLOGIA RESTAURADORA | pt_BR |
dc.publisher.initials | UFMG | pt_BR |
dc.relation.ispartof | International Endodontic Journal | pt_BR |
dc.rights | Acesso Restrito | pt_BR |
dc.subject | Dental pulp | pt_BR |
dc.subject | Dental bleaching | pt_BR |
dc.subject | Hemeoxygenase-1 | pt_BR |
dc.subject | hydrogen peroxide | pt_BR |
dc.subject | Jun-D | pt_BR |
dc.subject | Stem cells | pt_BR |
dc.subject.other | Dental pulp cavity | pt_BR |
dc.subject.other | Tooth bleaching | pt_BR |
dc.subject.other | Heme oxygenase-1 | pt_BR |
dc.subject.other | Hydrogen peroxide | pt_BR |
dc.subject.other | Stem cells | pt_BR |
dc.title | In vivo analysis of the presence of heme oxygenase-1, transcription factor Jun-D and CD90+/CD73+/CD105+/CD45- cells in the pulp of bleached teeth | pt_BR |
dc.type | Artigo de Periódico | pt_BR |
dc.url.externa | https://onlinelibrary.wiley.com/doi/full/10.1111/iej.13190 | pt_BR |
Appears in Collections: | Artigo de Periódico |
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