Local Application of a New Chalconic Derivative (Chalcone T4) Reduces Inflammation and Oxidative Stress in a Periodontitis Model in Rats
| dc.contributor.author | Camilli, Angelo Constantino [UNESP] | |
| dc.contributor.author | de Godoi, Mariely Araújo [UNESP] | |
| dc.contributor.author | Costa, Vitória Bonan [UNESP] | |
| dc.contributor.author | Fernandes, Natalie Aparecida Rodrigues [UNESP] | |
| dc.contributor.author | Cirelli, Giovani [UNESP] | |
| dc.contributor.author | da Silva, Larissa Kely Faustino [UNESP] | |
| dc.contributor.author | Assis, Letícia Ribeiro [UNESP] | |
| dc.contributor.author | Regasini, Luis Octavio [UNESP] | |
| dc.contributor.author | Guimarães-Stabili, Morgana Rodrigues [UNESP] | |
| dc.contributor.institution | Universidade Estadual Paulista (UNESP) | |
| dc.date.accessioned | 2025-04-29T18:05:36Z | |
| dc.date.issued | 2024-10-01 | |
| dc.description.abstract | Chalcones 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.affiliation | Department of Diagnosis and Surgery School of Dentistry at Araraquara São Paulo State University (UNESP), SP | |
| dc.description.affiliation | Department of Chemistry and Environmental Sciences Institute of Biosciences Humanities and Exact Sciences São Paulo State University (UNESP), SP | |
| dc.description.affiliationUnesp | Department of Diagnosis and Surgery School of Dentistry at Araraquara São Paulo State University (UNESP), SP | |
| dc.description.affiliationUnesp | Department of Chemistry and Environmental Sciences Institute of Biosciences Humanities and Exact Sciences São Paulo State University (UNESP), SP | |
| dc.identifier | http://dx.doi.org/10.3390/antiox13101192 | |
| dc.identifier.citation | Antioxidants, v. 13, n. 10, 2024. | |
| dc.identifier.doi | 10.3390/antiox13101192 | |
| dc.identifier.issn | 2076-3921 | |
| dc.identifier.scopus | 2-s2.0-85207667006 | |
| dc.identifier.uri | https://hdl.handle.net/11449/297112 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Antioxidants | |
| dc.source | Scopus | |
| dc.subject | antioxidant activity | |
| dc.subject | chalcone | |
| dc.subject | periodontitis | |
| dc.subject | topical application | |
| dc.title | Local Application of a New Chalconic Derivative (Chalcone T4) Reduces Inflammation and Oxidative Stress in a Periodontitis Model in Rats | en |
| dc.type | Artigo | pt |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 149311d1-6d9c-48c7-a080-10aa2b8bf4f4 | |
| relation.isAuthorOfPublication.latestForDiscovery | 149311d1-6d9c-48c7-a080-10aa2b8bf4f4 | |
| relation.isOrgUnitOfPublication | ca4c0298-cd82-48ee-a9c8-c97704bac2b0 | |
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| unesp.author.orcid | 0000-0003-4985-443X[1] | |
| unesp.author.orcid | 0009-0007-9632-2213[6] | |
| unesp.author.orcid | 0000-0001-9869-8934[7] | |
| unesp.author.orcid | 0000-0001-8574-0670[8] | |
| unesp.author.orcid | 0000-0002-1297-9717[9] | |
| unesp.campus | Universidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquara | pt |
| unesp.campus | Universidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Preto | pt |
