Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14365/4112
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dc.contributor.authorVatansever, H. Seda-
dc.contributor.authorÖzbilgin, Kemal-
dc.contributor.authorÖztatlıcı, Mustafa-
dc.contributor.authorTemel, Merve-
dc.contributor.authorİnan, Sevinç-
dc.date.accessioned2023-06-16T15:06:56Z-
dc.date.available2023-06-16T15:06:56Z-
dc.date.issued2020-
dc.identifier.issn2147-9607-
dc.identifier.urihttps://doi.org/10.34087/cbusbed.830175-
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/418030-
dc.identifier.urihttps://hdl.handle.net/20.500.14365/4112-
dc.description.abstractObjective: Ovarian cryopreservation is a useful alternative for fertility preservation in assisted reproductivetechnologies. In spite of many advances in the vitrification procedure, this technique is still considered experimental. Therefore in this study, we aimed to investigate the expressions of mitochondrial fusion (MFN1, MFN2 and OPA1), fission (DRP1), mitophagy (PARKIN, PINK1) and transport (MIRO-1, MILTON) proteins in ovarian tissues by qPCR technique after vitrification.Materials and Methods: To investigate the mitochondrial dynamics after vitrification, the ovaries were recoveredfrom 6-8 week old healthy female mice (No: 12) and were divided into vitrification and control groups. Vitrification carried out using ethylene glycol, dimethylsulfoxide and sucrose. After total RNA isolation from ovaries in control and vitrification groups, qPCR technique was performed to determine the expression rate of target genes. The relative gene expressions of the target genes were evaluated according to 2???Ct method.Results: Histological evaluation revealed that ovaries in the control group were shown normal morphology while the tissue integrity of the ovaries in the vitrification group is disrupted, some follicles are degenerated and granulosa cells were shed into antrum. According to our qPCR results, outer membran fusion proteins MFN1 gene expression decreased 1.12 fold and inner membran protein OPA-1 increased 1,36 fold in the vitrification group compared the control group. The mitochondrial fission protein DRP-1 gene expression increased 1.20 fold in the vitrification group. The mitophagy proteins PINK-1 and PARKIN genes expressions decreased 1.34 and 3.75 fold respectively in the vitrification group. The transport proteins; MIRO-1 gene expression decreased 1.16 fold but MILTON (TRAK-1) gene expression sharply increased 2,28 fold compared the control group.Conclusion: The alternation of the mitochondrial dynamics related gene expressions may lead a decrease in themitochondrial function during the ovarian vitrification and may reduce the potential of oocyte maturation and embryo development.en_US
dc.language.isoenen_US
dc.relation.ispartofCelal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleThe Effects of Ovarian Vitrification on Mitochondrial Fusion (mfn-1, Mfn 2 and Opa-1), Fission (dnm-1), Mitophagy (parkin, Pink-1) Andtransport (miro-1, Milton) Proteinsen_US
dc.typeArticleen_US
dc.identifier.doi10.34087/cbusbed.830175-
dc.departmentİzmir Ekonomi Üniversitesien_US
dc.identifier.volume7en_US
dc.identifier.issue4en_US
dc.identifier.startpage544en_US
dc.identifier.endpage550en_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.trdizinid418030en_US
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
crisitem.author.dept09.01. Basic Medical Sciences-
Appears in Collections:TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection
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