Kasai M, Hamaguchi Y, Zhu S E, Miyake T, Sakurai T, Machida T
Laboratory of Animal Science, College of Agriculture, Kochi University, Japan.
Biol Reprod. 1992 Jun;46(6):1042-6. doi: 10.1095/biolreprod46.6.1042.
Rabbit morulae were exposed to a vitrification solution-modified PBS [PB1] medium containing 40% ethylene glycol + 18% Ficoll + 0.3 M sucrose (EFS) for 2, 5, or 10 min at 20 degrees C and were vitrified in liquid nitrogen. When morulae were rapidly warmed, 96% had an intact zona pellucida. When embryos were cultured after removal of the mucin coat, high proportions of them formed blastocoel (79-100%), but the percentage of embryos developed to fully expanded blastocysts decreased with increased exposure time 87%, 40%, and 17%). The survival rate of morulae vitrified after removal of the mucin coat was lower than that of mucin-intact embryos. To assess the development potential in vivo, 131 embryos were vitrified after 2 min of exposure to EFS solution; all the embryos were recovered and 120 were transferred to recipients without removal of the mucin coat, resulting in 78 (65%) full-term fetuses or young. This simple method, which yields high survival both in vitro and in vivo, will be of practical use for vitrifying rabbit embryos.
将兔桑椹胚置于含有40%乙二醇+18%聚蔗糖+0.3M蔗糖(EFS)的玻璃化溶液改良PBS [PB1]培养基中,于20℃下处理2、5或10分钟,然后在液氮中进行玻璃化处理。当桑椹胚快速复温时,96%的胚透明带完整。当去除黏液膜后培养胚胎时,大部分胚胎形成了囊胚腔(79 - 100%),但随着暴露时间增加,发育为完全扩张囊胚的胚胎百分比下降(87%、40%和17%)。去除黏液膜后玻璃化的桑椹胚存活率低于黏液膜完整的胚胎。为评估体内发育潜能,131枚胚胎在暴露于EFS溶液2分钟后进行玻璃化处理;所有胚胎均被回收,120枚未去除黏液膜被移植到受体体内,产下78只(65%)足月胎儿或幼崽。这种在体外和体内均能产生高存活率的简单方法,将在兔胚胎玻璃化中具有实际应用价值。