Boric Acid Improved Cryopreserved Mouse Embryo Development
dc.contributor.authorid | 0000-0002-2365-7246 | |
dc.contributor.coauthor | askin, A. C. | |
dc.contributor.department | N/A | |
dc.contributor.kuauthor | Kocabay, Ahmet | |
dc.contributor.kuprofile | Other | |
dc.contributor.researchcenter | Koç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM) | |
dc.contributor.schoolcollegeinstitute | N/A | |
dc.date.accessioned | 2025-01-19T10:32:33Z | |
dc.date.issued | 2023 | |
dc.description.abstract | Boric 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.indexedby | WoS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 9 | |
dc.description.publisherscope | International | |
dc.description.sponsors | The 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.volume | 202 | |
dc.identifier.doi | 10.1007/s12011-023-03990-9 | |
dc.identifier.eissn | 1559-0720 | |
dc.identifier.issn | 0163-4984 | |
dc.identifier.quartile | Q2 | |
dc.identifier.scopus | 2-s2.0-85178440204 | |
dc.identifier.uri | https://doi.org/10.1007/s12011-023-03990-9 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/26443 | |
dc.identifier.wos | 1113155300001 | |
dc.keywords | Boric acid | |
dc.keywords | Vitrification | |
dc.keywords | SSV | |
dc.keywords | Mouse | |
dc.language | en | |
dc.publisher | Springernature | |
dc.relation.grantno | Koc University Research Center for Translational Medicine - Republic of Turkey Ministry of Development | |
dc.source | Biological Trace Element Research | |
dc.subject | Biochemistry | |
dc.subject | Molecular biology | |
dc.title | Boric Acid Improved Cryopreserved Mouse Embryo Development | |
dc.type | Journal Article |