Purpose To investigate the effects of cryo-storage duration in liquid nitrogen on oocyte cryo-survival, fertilization and embryonic development following vitrification and warming. Methods Mature mouse oocytes were vitrified with McGill Cryoleaf and stored in liquid nitrogen for a period of 8-10 days, 90-92 days and 180-182 days, respectively. After warming, the survived oocytes were inseminated by intracytoplasmic sperm injection (ICSI) and cultured for 120 h. The rates of oocyte cryo-survival, cleavage and embryonic development were compared.
Result(s)The oocyte cryo-survival rate declined following cryo-storage duration for 180-182 days (90.4±7.9%) compared to that of the other two groups (97.4±3.0% and 98.0± 3.3%). The fertilization rate in the group of 180-182 days (66.6±22.0%) was also significantly reduced (P<0.05) compared with the groups of 8-10 days (92.2±10.8%) and 90-92 days (94.7±9.1%). In addition, the number of embryos developed to the blastocyst stage declined significantly (P<0.05) following long cryo-storage duration (72.1± 8.2%, 25.2±3.8% and 5.5±13.6%, respectively). Conclusion(s) The cryo-survival, fertilization rate and embryonic development of mouse oocytes are affected significantly, in an adverse manner, by the cryo-storage duration in liquid nitrogen.