dc.contributor.author | Cevik, Mesut | |
dc.contributor.author | Tas, Arzu | |
dc.contributor.author | Akkoc, Tolga | |
dc.contributor.author | Bagis, Haydar | |
dc.contributor.author | Arat, Sezen | |
dc.date.accessioned | 2020-06-21T15:12:38Z | |
dc.date.available | 2020-06-21T15:12:38Z | |
dc.date.issued | 2009 | |
dc.identifier.issn | 1300-0128 | |
dc.identifier.uri | https://doi.org/10.3906/vet-0803-5 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12712/19039 | |
dc.description | BAGIS/0000-0002-1140-8058; | en_US |
dc.description | WOS: 000271745600005 | en_US |
dc.description.abstract | The 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(2) 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 mu m) for 25 mu s 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(2), 5% O(2), and 89% N(2) in humidified air at 39 degrees 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. | en_US |
dc.description.sponsorship | University of Ondokuz MayisOndokuz Mayis University [VET-011]; TUBITAKTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [TOVAG-104O360] | en_US |
dc.description.sponsorship | We wish to thank Dr. M. A. Cengiz for statistical analysis and S. Sekmen and G. Turgut for technical assistance. This study was supported by the University of Ondokuz Mayis (grant no: VET-011) and TUBITAK, (grant no: TOVAG-104O360) and was performed at TUBITAK-MRC, Genetic Engineering and Biotechnology Institute in Turkey. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Scientific Technical Research Council Turkey-Tubitak | en_US |
dc.relation.isversionof | 10.3906/vet-0803-5 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Maturation | en_US |
dc.subject | in vitro fertilization | en_US |
dc.subject | parthenogenetic oocyte activation | en_US |
dc.subject | embryo culture | en_US |
dc.title | A comparative study of parthenogenetic activation and in vitro fertilization of in vitro matured bovine oocytes | en_US |
dc.type | article | en_US |
dc.contributor.department | OMÜ | en_US |
dc.identifier.volume | 33 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.startpage | 393 | en_US |
dc.identifier.endpage | 399 | en_US |
dc.relation.journal | Turkish Journal of Veterinary & Animal Sciences | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |