Publication:
Treatment with melatonin enhances the embryo quality and the development of vitrified/warmed eight cell mouse embryos by solid surface vitrification (SSV)

dc.contributor.coauthorCaglar, Kubra
dc.contributor.coauthorArat, Sezen
dc.contributor.departmentN/A
dc.contributor.departmentN/A
dc.contributor.kuauthorKocabay, Ahmet
dc.contributor.kuauthorTaşkın, Ali Cihan
dc.contributor.kuprofileOther
dc.contributor.kuprofileOther
dc.contributor.researchcenterKoç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
dc.contributor.researchcenterKoç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
dc.contributor.schoolcollegeinstituteN/A
dc.contributor.schoolcollegeinstituteN/A
dc.contributor.yokid291296
dc.contributor.yokidN/A
dc.date.accessioned2024-11-10T00:09:49Z
dc.date.issued2020
dc.description.abstractBACKGROUND: Melatonin is an endocrine hormone secreted from the pineal gland located outside the blood-brain barrier. OBJECTIVE: In this study, in vitro propagated eight-cell mouse embryos were vitrified by the Solid Surface Vitrification (SSV) method and after thawing, their in vitro development and embryo qualities in melatonin added media were investigated. METHODS: Pronuclear stage embryos obtained from super ovulated B6CBAF1/J strain mice, were cultured until the eight-cell stage. Then these eight-cell embryos were vitrified by the SSV method and after thawing, cultured in melatonin added media at 37 degrees C and 5 %CO2 conditions until the blastocyst stage. RESULT: In the experimental period, in vitro embryo development rates of the control, SSV and +10(-12) M melatonin groups were observed as 97%, 86% and 93%, respectively. CONCLUSION: Our results indicated that melatonin addition slightly increased the development rates and total cell numbers of embryos vitrified by the SSV method.
dc.description.indexedbyScopus
dc.description.indexedbyWoS
dc.description.issue2
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsorshipRepublic of Turkey Ministry of Development
dc.description.sponsorshipTUBITAK - The Scientific and Technological Research Council of Turkey [TOVAG 114O638] The authors gratefully acknowledge use of the services and facilities of the Koc University Research Center for Translational Medicine (KUTTAM), funded by the Republic of Turkey Ministry of Development. The content is solely the responsibility of the authors and does not necessarily represent the official views of the Ministry of Development. This research was supported by a grant from TUBITAK - The Scientific and Technological Research Council of Turkey (Grant Number: TOVAG 114O638). This manuscript is derived from the Master's thesis of Kubra Caglar.
dc.description.volume41
dc.identifier.doiN/A
dc.identifier.eissn1742-0644
dc.identifier.issn0143-2044
dc.identifier.scopus2-s2.0-85106554057
dc.identifier.uriN/A
dc.identifier.urihttps://hdl.handle.net/20.500.14288/17180
dc.identifier.wos534629500002
dc.keywordsMelatonin
dc.keywordsVitrification
dc.keywordsSSV
dc.keywordsMouse
dc.keywordsEight-cell stage
dc.keywordsEmbryo development
dc.keywordsGene-expression profiles
dc.keywordsIn-vitro
dc.keywordsEquilibration time
dc.keywordsCulture-medium
dc.keywordsPronuclear
dc.keywordsStage
dc.keywordsSurvival
dc.keywordsOocyte
dc.keywordsCryopreservation
dc.keywordsSupplementation
dc.languageEnglish
dc.publisherCryo Letters
dc.sourceCryoletters
dc.subjectBiology
dc.subjectPhysiology
dc.titleTreatment with melatonin enhances the embryo quality and the development of vitrified/warmed eight cell mouse embryos by solid surface vitrification (SSV)
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0003-3196-821X
local.contributor.authorid0000-0002-2365-7246
local.contributor.kuauthorKocabay, Ahmet
local.contributor.kuauthorTaşkın, Ali Cihan

Files