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Immunohistochemical, tomographic and histological study on onlay bone graft remodeling. Part II: Calvarial bone

dc.contributor.authorPedrosa Júnior, Wagner Fernandes
dc.contributor.authorOkamoto, Roberta [UNESP]
dc.contributor.authorFaria, Paulo Esteves Pinto
dc.contributor.authorArnez, Maya Fernanda Manfrin
dc.contributor.authorXavier, Samuel Porfírio
dc.contributor.authorSalata, Luiz Antonio
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:24:01Z
dc.date.available2014-05-27T11:24:01Z
dc.date.issued2009-11-01
dc.description.abstractObjectives: Little information is available on the molecular events that occur during graft incorporation over time. The calvarial bone (Cb) grafts have been reported to produce greater responses compared with other donor regions in maxillofacial reconstructions, but the scientific evidences for this are still lacking. The objectives of this study are (1) to study the morphological pattern of Cb onlay bone grafts and compare them with the biological events through immunohistochemical responses and (2) to establish the effects of perforations in maintaining the volume and bone density of the receptor bed. Material and methods: Sixty New Zealand White rabbits were submitted to Cb onlay bone grafts on the mandible. In 30 rabbits, the receptor bed was perforated (perforated group), while for the remaining animals the bed was kept intact (non-perforated group). Six animals from each group were sacrificed at 5, 7, 10, 20 and 60 days after surgery. Histological sections from the grafted area were prepared for immunohistochemical and histological analyses. Immuno-labeling was found for proteins Osteoprotegerin (OPG), receptor activator of nuclear factor-κβ ligand (RANKL), alkaline phosphatase (ALP), osteopontin (OPN), vascular endothelial growth factor (VEGF), tartrate-resistant acid phosphatase (TRAP), Type I collagen (COL I) and osteocalcin (OC). The tomography examination [computerized tomography (CT) scan] was conducted just after surgery and at the sacrifice. Results: The histological findings revealed that the perforations contributed to higher bone deposition during the initial stages at the graft-receptor bed interface, accelerating the graft incorporation process. The results of the CT scan showed lower resorption for the perforated group (P≤0.05), and both groups showed high bone density rates at 60 days. This set of evidences is corroborated by the immunohistochemical outcomes indicating that proteins associated with revascularization and osteogenesis (VEGF, OPN, TRAP and ALP) were found in higher levels in the perforated group. Conclusions: These findings indicate that the bone volume of calvarial grafts is better maintained when the receptor bed is perforated, probably resulting from more effective graft revascularization and greater bone deposition. The process of bone resorption peaked between 20 and 60 days post-operatively in both groups although significantly less in the perforated group. © 2009 John Wiley & Sons A/S.en
dc.description.affiliationDept. of Oral and Maxillofacial Surgery and Periodontics Faculty of Dentistry of Ribeirao Preto University of Sao Paulo at Ribeirao Preto, Av. Do Cafe, S/n - Campus USP, 14040-904 - Ribeirão Preto SP
dc.description.affiliationDepartment of Oral and Maxillofacial Surgery Faculty of Dentistry of Araçatuba University of the State of São Paulo, Araçatuba, SP
dc.format.extent1254-1264
dc.identifierhttp://dx.doi.org/10.1111/j.1600-0501.2009.01747.x
dc.identifier.citationClinical Oral Implants Research, v. 20, n. 11, p. 1254-1264, 2009.
dc.identifier.doi10.1111/j.1600-0501.2009.01747.x
dc.identifier.issn0905-7161
dc.identifier.issn1600-0501
dc.identifier.lattes1566928219828056
dc.identifier.scopus2-s2.0-70350035562
dc.identifier.urihttp://hdl.handle.net/11449/71219
dc.language.isoeng
dc.relation.ispartofClinical Oral Implants Research
dc.relation.ispartofjcr4.305
dc.relation.ispartofsjr2,462
dc.relation.ispartofsjr2,462
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.subjectBone graft
dc.subjectCalvarial bone
dc.subjectCT imaging
dc.subjectImmunohistochemistry
dc.subjectRevascularization
dc.subjectacid phosphatase
dc.subjectacid phosphatase tartrate resistant isoenzyme
dc.subjectalkaline phosphatase
dc.subjectcollagen type 1
dc.subjectisoenzyme
dc.subjectosteocalcin
dc.subjectosteoclast differentiation factor
dc.subjectosteopontin
dc.subjectosteoprotegerin
dc.subjecttartrate-resistant acid phosphatase
dc.subjectvasculotropin A
dc.subjectanimal
dc.subjectbone development
dc.subjectbone regeneration
dc.subjectbone transplantation
dc.subjectcomparative study
dc.subjectcomputer assisted tomography
dc.subjectgraft survival
dc.subjectimmunohistochemistry
dc.subjectmale
dc.subjectmetabolism
dc.subjectmethodology
dc.subjectnonparametric test
dc.subjectosteolysis
dc.subjectphysiology
dc.subjectrabbit
dc.subjectskull
dc.subjectAcid Phosphatase
dc.subjectAlkaline Phosphatase
dc.subjectAnimals
dc.subjectBone Resorption
dc.subjectBone Transplantation
dc.subjectCollagen Type I
dc.subjectGraft Survival
dc.subjectIsoenzymes
dc.subjectMale
dc.subjectOsseointegration
dc.subjectOsteocalcin
dc.subjectOsteogenesis
dc.subjectOsteopontin
dc.subjectOsteoprotegerin
dc.subjectRabbits
dc.subjectRANK Ligand
dc.subjectSkull
dc.subjectStatistics, Nonparametric
dc.subjectTomography, X-Ray Computed
dc.subjectVascular Endothelial Growth Factor A
dc.titleImmunohistochemical, tomographic and histological study on onlay bone graft remodeling. Part II: Calvarial boneen
dc.typeArtigopt
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.author.lattes1566928219828056
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.departmentCiências Básicas - FOApt

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