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Establishing a Dual Murine Model to Explore the Interactions Between Diabetes and Periodontitis in Mice

dc.contributor.authorSilva, Bárbara R. [UNESP]
dc.contributor.authorHidalgo, Marco A. R. [UNESP]
dc.contributor.authorSilva, Renata C. L. [UNESP]
dc.contributor.authorde Avila, Erica D. [UNESP]
dc.contributor.authorFuentes, Deivys L. P. [UNESP]
dc.contributor.authorCarlos, Iracilda Z. [UNESP]
dc.contributor.authorFigueiredo, Ingrid D. [UNESP]
dc.contributor.authorCerri, Estela S. [UNESP]
dc.contributor.authorCerri, Paulo S. [UNESP]
dc.contributor.authorBaviera, Amanda M. [UNESP]
dc.contributor.authorde Molon, Rafael Scaf [UNESP]
dc.contributor.authorScarel-Caminaga, Raquel M. [UNESP]
dc.date.accessioned2026-06-26T17:24:10Z
dc.date.issued2025-06-11
dc.description.abstractThis study aimed to develop and validate a dual murine model integrating a high-fat diet (HFD) and a single streptozotocin (STZ) dose to induce diabetes mellitus (DM), alongside periodontitis (Perio) induced by ligature placement and oral inoculation with <i>Porphyromonas gingivalis</i> (<i>P. gingivalis</i>). The goal was to mimic human pathological conditions, creating a physiologically relevant environment to study the interplay between DM and Perio. A total of 128 six-week-old male C57BL/6J mice were randomly divided into four groups: Control, DM, Perio, and DM-P. DM was induced by HFD and STZ injection, and Perio by ligature placement and <i>P. gingivalis</i> infection. Evaluations occurred at baseline and days 7, 14, and 21. Alveolar bone loss was assessed by micro-computed tomography, and inflammation was examined histologically. DM mice showed elevated glucose levels and insulin resistance. Perio and DM-P groups experienced significant bone loss compared with Control and DM groups. The morphometric analysis revealed abundant inflammatory cells and reduced collagen fibers in Perio and DM-P groups, especially at day 7. This dual murine model successfully replicated the key features of DM and Perio, maintaining overall health of the animals, and good tolerability by those subjects to the stress of both interventional procedures.
dc.description.affiliationDepartment of Morphology, Genetics, Orthodontics and Pediatric Dentistry, School of Dentistry at Araraquara, São Paulo State University—UNESP, Araraquara 14801-903, SP, Brazil;, barbara.roque@unesp.br, (B.R.S.);, marco.rimachi@unesp.br, (M.A.R.H.);, renata.cl.silva@unesp.br, (R.C.L.S.);, estela.sasso@unesp.br, (E.S.C.);, paulo.cerri@unesp.br, (P.S.C.)
dc.description.affiliationDepartment of Diagnosis and Surgery, School of Dentistry at Araçatuba, Sao Paulo State University—UNESP, Araçatuba 16015-050, SP, Brazil;, erica.avila@unesp.br
dc.description.affiliationDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University—UNESP, Araraquara 14800-903, SP, Brazil;, deivys.leandro@unesp.br, (D.L.P.F.);, iracilda.zeppone@unesp.br, (I.Z.C.);, ingrid.delbone@unesp.br, (I.D.F.);, amanda.baviera@unesp.br, (A.M.B.)
dc.description.affiliationUnespDepartment of Morphology, Genetics, Orthodontics and Pediatric Dentistry, School of Dentistry at Araraquara, São Paulo State University—UNESP, Araraquara 14801-903, SP, Brazil;, barbara.roque@unesp.br, (B.R.S.);, marco.rimachi@unesp.br, (M.A.R.H.);, renata.cl.silva@unesp.br, (R.C.L.S.);, estela.sasso@unesp.br, (E.S.C.);, paulo.cerri@unesp.br, (P.S.C.)
dc.description.affiliationUnespDepartment of Diagnosis and Surgery, School of Dentistry at Araçatuba, Sao Paulo State University—UNESP, Araçatuba 16015-050, SP, Brazil;, erica.avila@unesp.br
dc.description.affiliationUnespDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University—UNESP, Araraquara 14800-903, SP, Brazil;, deivys.leandro@unesp.br, (D.L.P.F.);, iracilda.zeppone@unesp.br, (I.Z.C.);, ingrid.delbone@unesp.br, (I.D.F.);, amanda.baviera@unesp.br, (A.M.B.)
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1189680332
dc.identifier.dimensionspub.1189680332
dc.identifier.doi10.3390/ijms26125611
dc.identifier.issn1661-6596
dc.identifier.issn1422-0067
dc.identifier.orcid0000-0001-5521-424X
dc.identifier.orcid0000-0003-0161-3872
dc.identifier.orcid0000-0003-4240-9317
dc.identifier.orcid0000-0001-6681-1269
dc.identifier.orcid0000-0002-0084-3468
dc.identifier.orcid0000-0003-1558-2894
dc.identifier.orcid0000-0001-5756-5828
dc.identifier.orcid0000-0003-0987-5295
dc.identifier.orcid0000-0003-1110-6233
dc.identifier.orcid0000-0001-5068-0268
dc.identifier.orcid0000-0003-2678-0431
dc.identifier.pmcidPMC12192739
dc.identifier.pmid40565075
dc.identifier.urihttps://hdl.handle.net/11449/326748
dc.publisherMDPI
dc.relation.ispartofInternational Journal of Molecular Sciences; n. 12; v. 26; p. 5611
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceDimensions
dc.titleEstablishing a Dual Murine Model to Explore the Interactions Between Diabetes and Periodontitis in Mice
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
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relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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