Journal of Embryo Transfer 2010; 25(3): 189-193
Published online September 30, 2010
Copyright © The Korean Society of Animal Reproduction and Biotechnology.
조상래, 최선호, 최창용, 손준규, 이풍연, 고응규, 김현종, 연성흠, 손동수
농촌진흥청 국립축산과학원 가축유전자원시험장
We investigated the cleavage rate and blastocyst yield for each culture condition to enhance tolerance of cryo-preservation of bovine IVF embryo with relatively lower cryo-tolerance compared to in vivo embryo. The cleavage rate and blastocysts yield for CR1aa, IVMD, IVD, CR1aa+10% FBS were 73.2, 69.3, 72.8, 68.5% and 44.1, 30.8, 33.3, 48.0%, respectively. The values did not differ among each treatments without serum. For embryo vitrification, In vivo and In vitro blastocysts were exposed to VS1(10% glycerin, 0.1 M glucose, 0.1 M sucrose, PEG 1%) for 5 min, and VS2 (10% glycerin, 10% EG, 0.2 M glucose, 0.2 M sucrose, PEG 2%) for 5 min and then VS3 (10% glycerin, 30% EG, 0.3 M glucose, 0.3 M sucrose, PEG 3%) for 1 min. The exposed embryos were then loaded into the 0.25 ml plastic straws and then plunged into liquid nitrogen. The straws were held for period of 1 to 2 weeks before thawing. In embryo viability, no differences in blastocyst re-expansion rates were found between in vivo and in vitro embryos. whereas expansion-BL rates was significantly higher for in vivo-derived embryos (72.7%) when compared to in vitro-derived embryos (51.4%), respectively (P<0.05). In conclusion, our results indicate that combined use of CRIaa culture medium with vitrification might enhance tolerance of cryopreservation for bovine IVF embryo production.
Keywords: bovine, embryos, in vitro, in vivo, cryopreservation
Journal of Embryo Transfer 2010; 25(3): 189-193
Published online September 30, 2010
Copyright © The Korean Society of Animal Reproduction and Biotechnology.
조상래, 최선호, 최창용, 손준규, 이풍연, 고응규, 김현종, 연성흠, 손동수
농촌진흥청 국립축산과학원 가축유전자원시험장, 농촌진흥청 국립축산과학원 가축유전자원시험장, 농촌진흥청 국립축산과학원 가축유전자원시험장, 농촌진흥청 국립축산과학원 가축유전자원시험장, 농촌진흥청 국립축산과학원 가축유전자원시험장, 농촌진흥청 국립축산과학원 가축유전자원시험장, 농촌진흥청 국립축산과학원 가축유전자원시험장, 농촌진흥청 국립축산과학원 가축유전자원시험장, 농촌진흥청 국립축산과학원 가축유전자원시험장
조상래, 최선호, 최창용, 손준규, 이풍연, 고응규, 김현종, 연성흠, 손동수
농촌진흥청 국립축산과학원 가축유전자원시험장
We investigated the cleavage rate and blastocyst yield for each culture condition to enhance tolerance of cryo-preservation of bovine IVF embryo with relatively lower cryo-tolerance compared to in vivo embryo. The cleavage rate and blastocysts yield for CR1aa, IVMD, IVD, CR1aa+10% FBS were 73.2, 69.3, 72.8, 68.5% and 44.1, 30.8, 33.3, 48.0%, respectively. The values did not differ among each treatments without serum. For embryo vitrification, In vivo and In vitro blastocysts were exposed to VS1(10% glycerin, 0.1 M glucose, 0.1 M sucrose, PEG 1%) for 5 min, and VS2 (10% glycerin, 10% EG, 0.2 M glucose, 0.2 M sucrose, PEG 2%) for 5 min and then VS3 (10% glycerin, 30% EG, 0.3 M glucose, 0.3 M sucrose, PEG 3%) for 1 min. The exposed embryos were then loaded into the 0.25 ml plastic straws and then plunged into liquid nitrogen. The straws were held for period of 1 to 2 weeks before thawing. In embryo viability, no differences in blastocyst re-expansion rates were found between in vivo and in vitro embryos. whereas expansion-BL rates was significantly higher for in vivo-derived embryos (72.7%) when compared to in vitro-derived embryos (51.4%), respectively (P<0.05). In conclusion, our results indicate that combined use of CRIaa culture medium with vitrification might enhance tolerance of cryopreservation for bovine IVF embryo production.
Keywords: bovine, embryos, in vitro, in vivo, cryopreservation
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pISSN: 2671-4639
eISSN: 2671-4663