Logo do repositório

Local Application of a New Chalconic Derivative (Chalcone T4) Reduces Inflammation and Oxidative Stress in a Periodontitis Model in Rats

dc.contributor.authorCamilli, Angelo Constantino [UNESP]
dc.contributor.authorde Godoi, Mariely Araújo [UNESP]
dc.contributor.authorCosta, Vitória Bonan [UNESP]
dc.contributor.authorFernandes, Natalie Aparecida Rodrigues [UNESP]
dc.contributor.authorCirelli, Giovani [UNESP]
dc.contributor.authorda Silva, Larissa Kely Faustino [UNESP]
dc.contributor.authorAssis, Letícia Ribeiro [UNESP]
dc.contributor.authorRegasini, Luis Octavio [UNESP]
dc.contributor.authorGuimarães-Stabili, Morgana Rodrigues [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:05:36Z
dc.date.issued2024-10-01
dc.description.abstractChalcones are phenolic compounds with biological properties. This study had the aim to evaluate the effects of topical administration of a new synthetic chalcone, Chalcone T4, in an animal model of periodontitis induced by ligature. Forty rats were distributed in the following experimental groups: negative control (without periodontitis and topical application of distilled water), positive control (periodontitis and topical application of distilled water), chalcone I and II (periodontitis and topical application of 0.6 mg/mL and 1.8 mg/mL, respectively). Chalcone or distilled water was administered into the gingival sulcus of the first molars daily for 10 days, starting with the ligature installation. The following outcomes were evaluated: alveolar bone loss (µCT and methylene blue dye staining), quantification of osteoclasts (histomorphometry), cell infiltrate and collagen content (stereometry), gene expression of mediators (Nfact11, Tnf-α, Mmp-13, iNos, Sod and Nrf2) by (RT-qPCR); expression of BCL-2 and Caspase-1 (immunohistochemistry). Chalcone T4 inhibited bone resorption and prevented collagen matrix degradation. Reduction in the expression of inflammatory markers (Nfact11, Tnf-α, Mmp-13, and Caspase-1), attenuation of oxidative stress (iNOS reduction, and increase in Sod), and pro-apoptotic effect of the compound (BCL-2 reduction), were associated its effects on periodontal tissues. Topical application of Chalcone T4 prevented bone resorption and inflammation, demonstrating potential in the adjunctive treatment of periodontitis.en
dc.description.affiliationDepartment of Diagnosis and Surgery School of Dentistry at Araraquara São Paulo State University (UNESP), SP
dc.description.affiliationDepartment of Chemistry and Environmental Sciences Institute of Biosciences Humanities and Exact Sciences São Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Diagnosis and Surgery School of Dentistry at Araraquara São Paulo State University (UNESP), SP
dc.description.affiliationUnespDepartment of Chemistry and Environmental Sciences Institute of Biosciences Humanities and Exact Sciences São Paulo State University (UNESP), SP
dc.identifierhttp://dx.doi.org/10.3390/antiox13101192
dc.identifier.citationAntioxidants, v. 13, n. 10, 2024.
dc.identifier.doi10.3390/antiox13101192
dc.identifier.issn2076-3921
dc.identifier.scopus2-s2.0-85207667006
dc.identifier.urihttps://hdl.handle.net/11449/297112
dc.language.isoeng
dc.relation.ispartofAntioxidants
dc.sourceScopus
dc.subjectantioxidant activity
dc.subjectchalcone
dc.subjectperiodontitis
dc.subjecttopical application
dc.titleLocal Application of a New Chalconic Derivative (Chalcone T4) Reduces Inflammation and Oxidative Stress in a Periodontitis Model in Ratsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isAuthorOfPublication149311d1-6d9c-48c7-a080-10aa2b8bf4f4
relation.isAuthorOfPublication.latestForDiscovery149311d1-6d9c-48c7-a080-10aa2b8bf4f4
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.author.orcid0000-0003-4985-443X[1]
unesp.author.orcid0009-0007-9632-2213[6]
unesp.author.orcid0000-0001-9869-8934[7]
unesp.author.orcid0000-0001-8574-0670[8]
unesp.author.orcid0000-0002-1297-9717[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt

Arquivos