Al-Hasani S, Trotnow S, Barthel M
Geburtshilfe Frauenheilkd. 1982 Dec;42(12):848-52. doi: 10.1055/s-2008-1037170.
Rabbit embryos were successfully frozen at the 8-cell stage, employing a rapid and a slow freezing-thawing program. They were then stored at -196 degrees C (liquid nitrogen) for 10 to 60 days. After thawing the embryos were examined for viability in vitro and in vivo. Using the slow program B 82.5% were morphologically intact, compared to only 69.3% after the rapid procedure (program A). 88.8% of the group first mentioned above, and 56.8% of the latter developed to the blastocyst stage after 4 to 5 days in culture. The implantation rate was 18.1%, when embryos were transferred to minus 18 hours asynchronous recipients, after thawing. With 40%, a significantly higher implantation rate could be achieved, when the embryos were transferred to minus 24 hours asynchronous foster mothers. 18 viable young were born 30 to 32 days after transfer.
采用快速和慢速冻融程序,兔胚胎在8细胞阶段成功冷冻。然后将它们储存在-196℃(液氮)中10至60天。解冻后,对胚胎进行体外和体内活力检查。使用慢速程序B,82.5%的胚胎形态完整,而快速程序(程序A)后只有69.3%。上述第一组的88.8%和后者的56.8%在培养4至5天后发育到囊胚阶段。解冻后将胚胎转移到相差18小时的同期受体时,着床率为18.1%。当胚胎转移到相差24小时的同期代孕母兔时,着床率可显著提高到40%。转移后30至32天出生了18只存活幼崽。