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dc.contributor.authorKocyigit, Alper
dc.contributor.authorCevik, Mesut
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:48:15Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:48:15Z
dc.date.issued2015
dc.identifier.issn0011-2240
dc.identifier.issn1090-2392
dc.identifier.urihttps://dx.doi.org/10.1016/j.cryobiol.2015.05.068
dc.identifier.urihttps://hdl.handle.net/20.500.12418/7781
dc.descriptionWOS: 000358632700009en_US
dc.descriptionPubMed ID: 26025880en_US
dc.description.abstractThe present study examined the developmental capacity and cryotolerance of cultured bovine embryos in defined media (synthetic oviduct fluid, SOF) supplemented with insulin-like growth factor I (IGF-I) and leukemia inhibitor factor (LIF). The objectives of the present study were: (1) to examine the effects IGF-I and LIP on bovine embryo development potential and (2) to investigate the cryotolerance and survivability of vitrified blastocysts obtained from embryos cultured in a defined media. We studied the development of bovine embryos produced in vitro and cultured (in four different treatments) until Day 7 after fertilization. In Experiment 1, zygotes were cultured to the blastocyst stage and differentially stained for determine the count of cells. In Experiment 2, zygotes were vitrified before staining. LIF alone or combined with IGF-I was significantly effective on in vitro bovine embryo development especially ratio to reach blastocyst. The cells for both ICM and TE decreased by the effect of freezing in all treatment groups in the Experiment 2 compared with Experiment I. Interestingly, the LIF treatment showed fewest variations. In addition to this, for average number of ICM and TE cells, LIP treatment showed fewest variation compared with other treatments (ICM: 23.5 vs 19.5, TE: 53.6 vs 51). These results are the first to demonstrate that the addition of IGF-I along with LIP to the culture medium was found to be beneficial for bovine embryonic development based on cellular cryotolerance after vitrification. (C) 2015 Elsevier Inc. All rights reserved.en_US
dc.description.sponsorshipResearch Foundation of Ondokuz Mayis University, Samsun/TURKEY [ID: PYO.VET.1904.11.011]en_US
dc.description.sponsorshipStatement of funding: This work was funded by the Research Foundation of Ondokuz Mayis University, Samsun/TURKEY. This article was produced by the same name PhD thesis study. Project ID: PYO.VET.1904.11.011.en_US
dc.language.isoengen_US
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCEen_US
dc.relation.isversionof10.1016/j.cryobiol.2015.05.068en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBovine blastocysten_US
dc.subjectGrowth factoren_US
dc.subjectCytokineen_US
dc.subjectVitrificationen_US
dc.subjectCryotoleranceen_US
dc.titleEffects of leukemia inhibitory factor and insulin-like growth factor-I on the cell allocation and cryotolerance of bovine blastocystsen_US
dc.typearticleen_US
dc.relation.journalCRYOBIOLOGYen_US
dc.contributor.department[Kocyigit, Alper] Cumhuriyet Univ, Fac Vet Med, Dept Reprod & Artificial Inseminat, Sivas, Turkey -- [Cevik, Mesut] Ondokuz Mayis Univ, Dept Reprod & Artificial Inseminat, Fac Vet Med, Samsun, Turkeyen_US
dc.contributor.authorIDKOCYIGIT, Alper -- 0000-0001-9639-5497en_US
dc.identifier.volume71en_US
dc.identifier.issue1en_US
dc.identifier.endpage69en_US
dc.identifier.startpage64en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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