Evaluation of chondrogenesis and osteogenesis via Wnt/?-Catenin, S100 immunoexpression and histomorphometry in fetal rats following maternal uterine artery ligation

dc.contributor.authorUslu, Serap
dc.contributor.authorÖktem, Gülperi
dc.contributor.authorOltulu, Fatih
dc.contributor.authorDemir, Kenan
dc.contributor.authorİrban, Arzu
dc.contributor.authorBasdemir, Gulcin
dc.contributor.authorİnce, Ümit
dc.date.accessioned2025-05-10T13:59:53Z
dc.date.issued2020
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractAim: The aim of this study is to investigate the effects of intrauterine growth retardation depending onmaternal uterine artery ligation model, Wnt/?-catenin and S100 expression immunohistochemistry andhistomorphometrically on growth plate and bone tissue of fetal rats.Materials and Methods: Maternal rats were randomly divided into 3 groups (n=5). No surgery oranesthesia were applied in control group. Bilaterally the maternal uterine arteries were ligated ongestational day 18 in experimental group. Although all surgical procedures were performed in shamgroup, the uterine artery ligation were not made. Fetuses were taken on gestational day 20,thicknesses of growth plate and zones, trabecular number and thickness and cortical thickness wereevaluated with the histomorphometrically in samples from left proximal tibia. The expressions of ?catenin and S100 immunohistochemically were evaluated in the growth plate.Results: Thicknesses of growth plate (p<0.01), proliferation zone (p<0.05) and degeneration zone(p<0.01) were measured significantly thinner in experimental group than the others and thicknesses ofhypertrophic zones were lesser than the control and sham group, but the results were not statisticallysignificant (p>0.05). Also trabecular numbers were lower (p<0.01) and trabecular thickness were alsothinner (p<0.05) in experimental group. Expression of ?-catenin was declined and S100 expressionwas increased in experimental group.Conclusion: We conclude that maternal uterine artery ligation, leads to shortness of growth plate anddegenerated bone architecture because of Wnt/?-catenin signaling pathway.
dc.identifier.endpage46
dc.identifier.issn1016-9113
dc.identifier.issn2147-6500
dc.identifier.issue1
dc.identifier.startpage39
dc.identifier.trdizinid386620
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/386620
dc.identifier.urihttps://hdl.handle.net/20.500.14730/3874
dc.identifier.volume59
dc.indekslendigikaynakTR-Dizin
dc.language.isoen
dc.relation.ispartofEge Tıp Dergisi
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_TR-Dizin_20250302
dc.subjectBiyoloji
dc.subjectTıbbi Araştırmalar Deneysel
dc.subjectZooloji
dc.titleEvaluation of chondrogenesis and osteogenesis via Wnt/?-Catenin, S100 immunoexpression and histomorphometry in fetal rats following maternal uterine artery ligation
dc.typeArticle

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