Publication:
A Comparative Study of Parthenogenetic Activation and In Vitro Fertilization of In Vitro Matured Bovine Oocytes

dc.authorscopusid23396214300
dc.authorscopusid24472081300
dc.authorscopusid23767133200
dc.authorscopusid55919600100
dc.authorscopusid6603553213
dc.contributor.authorÇevi̇k, M.
dc.contributor.authorTas Ekiz, A.
dc.contributor.authorAkkoç, T.
dc.contributor.authorBaǧiş, H.
dc.contributor.authorArat, S.
dc.date.accessioned2020-06-21T15:12:38Z
dc.date.available2020-06-21T15:12:38Z
dc.date.issued2009
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Çevi̇k] Mesut, Faculty of Veterinary Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Tas Ekiz] Arzu, TUBITAK Marmara Research Center, Gebze, Kocaeli, Turkey; [Akkoç] Tolga, TUBITAK Marmara Research Center, Gebze, Kocaeli, Turkey; [Baǧiş] Haydar, TUBITAK Marmara Research Center, Gebze, Kocaeli, Turkey; [Arat] Sezen, TUBITAK Marmara Research Center, Gebze, Kocaeli, Turkeyen_US
dc.description.abstractThe objective of this study was to determine the effects of 3 chemical agents used sequentially and electrical stimuli on parthenogenetic activation of in vitro matured bovine oocytes and comparison with a standard IVF protocol for embryo developmental rates. For this purpose, oocytes were matured in tissue culture medium-199 (TCM-199) at 39 °C and 5% of CO<inf>2</inf> in humidified air. For IVF, matured oocytes were fertilized in Modified Tyrode-Lactate Medium. In the parthenogenetic activation process, direct current (DC) was pulsed (133 V/500 μm) for 25 μs and oocytes were sequentially activated with calcium ionophore (CaI) for 10 min, cycloheximide (CHX) + cytochalasin D for 1 h, and CHX for 5 h. After that, all embryos (both IVF and parthenogenetic) were cultured in G1.3/G2.3 media containing 6% CO<inf>2</inf>, 5% O<inf>2</inf>, and 89% N<inf>2</inf> in humidified air at 39 °C. Cleavage rate was not significantly different following parthenogenetic activation compared to IVF (P > 0.05). Morula, blastocyst development, and blastocyst cell numbers were not also significantly different between parthenogenetic activation and IVF (P > 0.05). These results showed that bovine oocyte activation with electrical stimulation and chemical agents gave the desirable results, and the culture medium (G1.3/G2.3) supported both parthenogenetic and IVF embryo development. © TÜBİTAK.en_US
dc.identifier.doi10.3906/vet-0803-5
dc.identifier.endpage399en_US
dc.identifier.issn1300-0128
dc.identifier.issn1303-6181
dc.identifier.issue5en_US
dc.identifier.scopus2-s2.0-77449106118
dc.identifier.scopusqualityQ3
dc.identifier.startpage393en_US
dc.identifier.urihttps://doi.org/10.3906/vet-0803-5
dc.identifier.volume33en_US
dc.identifier.wosWOS:000271745600005
dc.identifier.wosqualityQ3
dc.language.isotren_US
dc.publisherTÜBİTAK erdin@metu.edu.tren_US
dc.relation.ispartofTurkish Journal of Veterinary & Animal Sciencesen_US
dc.relation.journalTurkish Journal of Veterinary & Animal Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectEmbryo Cultureen_US
dc.subjectIn Vitro Fertilizationen_US
dc.subjectMaturationen_US
dc.subjectParthenogenetic Oocyte Activationen_US
dc.titleA Comparative Study of Parthenogenetic Activation and In Vitro Fertilization of In Vitro Matured Bovine Oocytesen_US
dc.title.alternativeİn Vitro Mature Edilmiş Sıǧır Oositlerinin Partenogenetik Aktivasyonu ve İn Vitro Fertilizasyonunun Karşılaptırmalı Çalışmasıen_US
dc.typeArticleen_US
dspace.entity.typePublication

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