The histopathological evaluation of effects of application of the bovine amniotic fluid with graft on peri-implant bone regeneration

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dc.authorid0000-0002-7536-7064en_US
dc.authorid0000-0003-3815-8543en_US
dc.authorid0000-0002-8407-5792en_US
dc.authorid0000-0002-4907-6159en_US
dc.authorid0000-0001-6513-0226en_US
dc.authorid0000-0003-4750-9798en_US
dc.authorid0000-0003-3944-1957en_US
dc.contributor.authorİstek, Özmen
dc.contributor.authorTanrısever, Murat
dc.contributor.authorEröksüz, Hatice
dc.contributor.authorKarabulut, Burak
dc.contributor.authorÖzcan, Erhan Cahit
dc.contributor.authorBingül, Muhammet Bahattin
dc.contributor.authorGüler, Rıdvan
dc.contributor.authorDündar, Serkan
dc.date.accessioned2023-10-26T08:01:25Z
dc.date.available2023-10-26T08:01:25Z
dc.date.issued2023en_US
dc.departmentDicle Üniversitesi, Diş Hekimliği Fakültesi, Ağız-Diş-Çene Hastalıkları ve Cerrahisi Bölümüen_US
dc.description.abstractThis study aimed to determine the effects of bovine amniotic fluid combined with bone graft in treating peri-implant bone defects with guided bone regeneration. Twenty female Sprague–Dawley rats were divided into two groups. Bone sockets with a diameter of 4 mm in the coronal part and a diameter of 2.5 mm in the apical part of the implant were created into the corticocancellous bone in the metaphyseal parts of the right tibia bones of all subjects. Implants with a length of 4 mm and a diameter of 2.5 mm were placed in the bone sockets. In the sham surgery group (n = 10) was the circumferential bone defect equivalent to half of the 4-mm implant length, which occurred between the implant and the bone, filled with bovine xenograft. Bovine xenografts were filled with amniotic fluid mixture in the experimental group (n = 10). After 8 weeks of recovery, all rats were sacrificed. The implants were extracted from the soft tissues and the surrounding bone. Subsequently, the bones were decalcified and prepared for histological analysis. The percentage of newly regenerated bone (NRB) formation and fibrosis in the bone defect area around the implant was calculated from all sections. NRB was found in 37.4±4.4% of controls and 41.4±2.63% of test animals (P<0.05 and P=0.024, respectively). Fibrosis formation was found at a rate of 38.6±5.06% in the control group and 33.2±5.38% in the test group (P<0.05 and P=0.033, respectively). It was considered that combining bovine amniotic fluid with bone transplant could be a useful way of treating bone abnormalities.en_US
dc.identifier.citationİstek, Ö., Tanrısever, M., Eröksüz, H., Karabulut, B., Özcan, E. C., Bingül, M. B. ve diğerleri. (2023). The histopathological evaluation of effects of application of the bovine amniotic fluid with graft on peri-implant bone regeneration. Kafkas Universitesi Veteriner Fakultesi Dergisi, 23(5), 551-556.en_US
dc.identifier.doi10.9775/kvfd.2023.30031
dc.identifier.endpage556en_US
dc.identifier.issn1300-6045
dc.identifier.issue5en_US
dc.identifier.scopus2-s2.0-85172341821
dc.identifier.scopusqualityQ3
dc.identifier.startpage551en_US
dc.identifier.urihttps://vetdergikafkas.org/uploads/pdf/pdf_KVFD_3032.pdf
dc.identifier.urihttps://hdl.handle.net/11468/12950
dc.identifier.volume23en_US
dc.identifier.wosWOS:001074211700001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthorGüler, Rıdvan
dc.language.isoenen_US
dc.publisherKafkas Universitesi Veteriner Fakultesien_US
dc.relation.ispartofKafkas Universitesi Veteriner Fakultesi Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBone graften_US
dc.subjectBovine amniotic fluiden_US
dc.subjectGuided bone regenerationen_US
dc.subjectPeri-implant bone defecten_US
dc.subjectTibial boneen_US
dc.titleThe histopathological evaluation of effects of application of the bovine amniotic fluid with graft on peri-implant bone regenerationen_US
dc.titleThe histopathological evaluation of effects of application of the bovine amniotic fluid with graft on peri-implant bone regeneration
dc.typeArticleen_US

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