Intra-articular human deciduous dental pulp stem cell administration vs. pharmacological therapy in experimental osteoarthritis rat model

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dc.contributor(LG) Lab. Genéticapt_BR
dc.contributor.authorMaldonado, D. Correapt_BR
dc.contributor.authorNicoliche, T.pt_BR
dc.contributor.authorFaber, J.pt_BR
dc.contributor.authorKerkis, Irinapt_BR
dc.contributor.authorSaez, D. Martinezpt_BR
dc.contributor.authorSasaki, R. Tetsuopt_BR
dc.contributor.authorSilva, M. Cavenaghi Pereira dapt_BR
dc.date.accessioned2021-06-11T17:12:51Z-
dc.date.available2021-06-11T17:12:51Z-
dc.date.issued2021pt_BR
dc.identifier.citationMaldonado D.C, Nicoliche T., Faber J., Kerkis I, Saez D.M, Sasaki R.T, et al. Intra-articular human deciduous dental pulp stem cell administration vs. pharmacological therapy in experimental osteoarthritis rat model. Eur. Rev. Med. Pharmacol. Sci.. 2021 ;25(9):3546-3556. doi:10.26355/eurrev_202105_25837.pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/3827-
dc.description.abstractOBJECTIVE: The aim of the present study was to compare the molecular and morphological effects of diacerein and glucosamine-chondroitin drug treatment and intra-articular injection herapy of human deciduous dental pulp stem cells (hDPSCs) in a rat knee model of induced osteoarthritis OA. MATERIALS AND METHODS: Thirty-six adult male rats were randomly separated into six groups: Control group without induction of OA, osteoarthritis group 60 induction of OA, saline gavage started on day 14 and performed for 60 days, followed by euthanasia, osteoarthritis group induction of OA and euthanasia after 14 days, diacerein group, glucosamine-chondroitin group, and mesenchymal stem cell group. The drug-treated groups were gavaged with 50 mg/kg of diacerein and 400/500 mg/kg of glucosamine-chondroitin starting on dat 14 for 60 days. The cell therapy-treated group received an intra-articular single dose of 8 × 105 hDPSCs on day 14, and euthanasia was performed after 60 days. Lateral femoral condyles were collected and prepared for immunohistochemistry and light microscopy procedures. RESULTS: The morphological features and immunoexpression of SOX-5, IHH, MMP-8, MMP-13, and Type II collagen were statistically analysed. Our data suggest that hDPSC therapy contributes more actively and effectively in the structural reorganization of lateral femoral condyles. In contrast, the glucosamine-chondroitin sulphate treatment was more effective in inflammatory control, while diacerein showed better results associated with the maintenance of the primordial cartilage. CONCLUSIONS: The positive therapeutic effect of daily administered conventional drugs can be confirmed in a rat model of OA. However, one single dose of locally administered hDPSCs provides significant improvement in tissue regeneration in an OA model.pt_BR
dc.description.sponsorship(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulopt_BR
dc.format.extent3546-3556pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofEuropean Review for Medical and Pharmacological Sciencespt_BR
dc.rightsRestricted accesspt_BR
dc.titleIntra-articular human deciduous dental pulp stem cell administration vs. pharmacological therapy in experimental osteoarthritis rat modelpt_BR
dc.typeArticlept_BR
dc.identifier.doi10.26355/eurrev_202105_25837pt_BR
dc.identifier.urlhttps://doi.org/10.26355/eurrev_202105_25837pt_BR
dc.contributor.external(UNIFESP) Universidade Federal de São Paulopt_BR
dc.contributor.external(UNIFAL-MG) Universidade Federal de Alfenaspt_BR
dc.contributor.external(UFMT) Universidade Federal de Mato Grossopt_BR
dc.identifier.citationvolume25pt_BR
dc.identifier.citationissue9pt_BR
dc.subject.keywordOsteoarthritispt_BR
dc.subject.keywordGlucosaminept_BR
dc.subject.keywordChondroitinpt_BR
dc.subject.keywordDental pulp stem cellspt_BR
dc.relation.ispartofabbreviatedEur Rev Med Pharmacol Scipt_BR
dc.identifier.citationabntv. 25, n. 9, p. 3546-3556pt_BR
dc.identifier.citationvancouver2021 ;25(9):3546-3556pt_BR
dc.contributor.butantanKerkis, Irina|:Pesquisador:Docente permanente PPGTOX|:Lab. Genéticapt_BR
dc.sponsorship.butantanFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)¦¦2018/11235-2pt_BR
dc.sponsorship.butantanFundação Butantan¦¦pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
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item.languageiso639-1English-
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