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Use of local melatonin with xenogeneic bone graft to treat critical-size bone defects in rats with osteoporosis: a randomized study

dc.contributor.authorCosta, Karen Laurene Dalla
dc.contributor.authorAbreu, Letícia Furtado
dc.contributor.authorTolomei, Camila Barreto
dc.contributor.authorEleutério, Rachel Gomes
dc.contributor.authorBasting, Rosanna
dc.contributor.authorBalbinot, Gabriela
dc.contributor.authorCollares, Fabrício Mezzomo
dc.contributor.authorLopes, Pedro
dc.contributor.authorVeiga, Nelio
dc.contributor.authorFernandes, Gustavo Vicentis Oliveira
dc.contributor.authorPeruzzo, Daiane Cristina
dc.date.accessioned2024-06-18T16:02:22Z
dc.date.available2024-06-18T16:02:22Z
dc.date.issued2024-05-13
dc.description.abstractThe aim of this study was to evaluate the effect of local administration of melatonin (MLT) on molecular biomarkers and calvaria bone critical defects in female rats with or without osteoporosis, associated or not with a xenogeneic biomaterial. Forty-eight female rats were randomly divided into two groups: (O) ovariectomized and (S) placebo groups. After 45 days of osteoporosis induction, two critical-size defects (5 mm diameter) were created on the calvaria. The groups were subdivided according to the following treatment: (C) Clot, MLT, MLT associated with Bio-Oss® (MLTBO), and Bio-Oss® (BO). After 45 days, the defect samples were collected and processed for microtomography, histomorphometry, and biomolecular analysis (Col-I, BMP-2, and OPN). All animals had one femur harvested to confirm the osteoporosis. Microtomography analysis demonstrated a bone mineral density reduction in the O group. Regarding bone healing, the S group presented greater filling of the defects than the O group; however, in the O group, the defects treated with MLT showed higher mineral filling than the other treatments. There was no difference between the treatments performed in the S group (p = 0.05). Otherwise, O-MLT had neoformed bone higher than in the other groups (p = 0.05). The groups that did not receive biomaterial demonstrated lower levels of Col-I secretion; S-MLT and S-MLTBO presented higher levels of OPN, while O-C presented statistically lower results (p < 0.05); O-BO showed greater BMP-2 secretion (p < 0.05). In the presence of ovariectomy-induced osteoporosis, MLT treatment increased the newly formed bone area, regulated the inflammatory response, and increased OPN expression.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.3390/jfb15050124pt_PT
dc.identifier.eid85195109478
dc.identifier.issn2079-4983
dc.identifier.pmid38786635
dc.identifier.urihttp://hdl.handle.net/10400.14/45523
dc.identifier.wos001233126400001
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectCritical-size defectspt_PT
dc.subjectBone mineral densitypt_PT
dc.subjectMelatoninpt_PT
dc.subjectBone regenerationpt_PT
dc.subjectIn vivo studypt_PT
dc.titleUse of local melatonin with xenogeneic bone graft to treat critical-size bone defects in rats with osteoporosis: a randomized studypt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage16pt_PT
oaire.citation.issue5pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleJournal of Functional Biomaterialspt_PT
oaire.citation.volume15pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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