Boric Acid Improved Cryopreserved Mouse Embryo Development

dc.contributor.authorid0000-0002-2365-7246
dc.contributor.coauthoraskin, A. C.
dc.contributor.departmentN/A
dc.contributor.kuauthorKocabay, Ahmet
dc.contributor.kuprofileOther
dc.contributor.researchcenterKoç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
dc.contributor.schoolcollegeinstituteN/A
dc.date.accessioned2025-01-19T10:32:33Z
dc.date.issued2023
dc.description.abstractBoric acid (BA) is an essential trace element that is required to support the metabolic pathways in plants, humans, and animals. The present study investigates the in vitro development and quality of single-cell mouse embryos in a BA-added culture medium after cryopreservation using the solid-surface vitrification method. For this purpose, the pronuclear-stage embryos derived from superovulated C57Bl/6j mouse strains and the one-cell embryos were then cryopreserved using the solid-surface vitrification (SSV) method. After thawing, the embryos were cultured in a BA-added medium at 37 degrees C in a 5% CO2 environment until the blastocyst stage. The resulting in vitro development rates of the embryos in the control group, SSV group, and SSV + 1.62 x 10-4 mu M BA group were 68.11% (36/59), 40.16% (16/48), and 64.92% (28/48) respectively, indicating that the BA supported the in vitro development of the embryos cryopreserved using the SSV method. Our results suggest that the addition of boric acid to the culture media increased the development rate of the embryos that were vitrified using the SSV method.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue9
dc.description.publisherscopeInternational
dc.description.sponsorsThe authors gratefully acknowledge the 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.
dc.description.volume202
dc.identifier.doi10.1007/s12011-023-03990-9
dc.identifier.eissn1559-0720
dc.identifier.issn0163-4984
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85178440204
dc.identifier.urihttps://doi.org/10.1007/s12011-023-03990-9
dc.identifier.urihttps://hdl.handle.net/20.500.14288/26443
dc.identifier.wos1113155300001
dc.keywordsBoric acid
dc.keywordsVitrification
dc.keywordsSSV
dc.keywordsMouse
dc.languageen
dc.publisherSpringernature
dc.relation.grantnoKoc University Research Center for Translational Medicine - Republic of Turkey Ministry of Development
dc.sourceBiological Trace Element Research
dc.subjectBiochemistry
dc.subjectMolecular biology
dc.titleBoric Acid Improved Cryopreserved Mouse Embryo Development
dc.typeJournal Article

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