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作 者:王珂[1] 郭海龙[1] 桑国俊[1] 赵兴绪[2]
机构地区:[1]甘肃省畜牧兽医研究所,甘肃平凉744000 [2]甘肃农业大学动物医学院,甘肃兰州700070
出 处:《动物医学进展》2009年第3期40-43,共4页Progress In Veterinary Medicine
基 金:甘肃省生物工程项目;“牛胚胎规模化生产及相关新技术开发”项目
摘 要:采用OPS管和GMP管对GV期的牛的卵母细胞进行玻璃化冷冻。在不同的前处理液中平衡5min,然后在冷冻液(EFS30,EFS40,EDFS30或EDFS40)中平衡30s,进行OPS法和GMP法玻璃化冷冻保存。结果显示,OPS法用EFS40液和EDFS40液冷冻后形态正常卵率为69.6%和76.1%,2组差异显著(P<0.05),成熟率最高达19.2%和33.3%,2组差异显著(P<0.05);GMP法用EFS40液和EDFS40液冷冻后形态正常卵率最高达75.6%和80.8%,2组差异显著(P<0.05),成熟率最高达15.6%和34.9%,2组差异显著(P<0.05)。而采用EDFS40液,OPS法和GMP法对GV期卵母细胞体外发育的影响差异均不显著,但GMP法的冷冻效率较高。表明采用EDFS40液GMP法对GV期卵母细胞的冷冻效率优于OPS法。Cow GV(germinal vesicle) stage oocytes were respectively vitrified in EFS30, EFS40, EDFS30 and EDFS40 by a two-step method with the different carrier(OPS&GMP). Kept in pre-balance solution in 5 minutes and different frozen solutions in 30 s, the cow GV oocytes were vitrified with OPS&GMP. In cow GV oocytes vitrified by OPS, 69.6% oocytes were morphologically normal in EFS40 solution after thawing and 76.1% in EDFS40 solution (P〈0.05). The mature rate was 17.2% in EFS40 solution and 35% in EDFS40 solution (P〈0.05). While in bovine's GV oocytes vitrified by GMP, 75.6% oocytes were morphologically normal in EFS40 solution and 80.8% in EDFS40 solution (P〈0.05), the mature rate was 15.6% in EFS40 solution after thawing and 34.9% in EDFS40 solution (P〈0.05). Effects of carrier (OPS&GMP) on verifications of cow GV oocytes were not significantly different (P〉0.05),but effects of cow GV oocytes vitrified in EDFS40 by the two-step method with GMP were better than that in others.
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