Superovulated hamster oocytes were frozen by 2 M DMSO. 89% (499/561) o
f the oocytes survived freezing and thawing. A hamster-ICSI assay was
performed to evaluate the ability of frozen-thawed oocytes to develop
male pronuclei. 46% (58/127) of the oocytes had male pronuclear format
ion following injection of single human sperm into the cytoplasm of fr
ozen-thawed oocytes. There was no significant difference in male pronu
clear formation as compared with fresh oocytes. This study shows that
hamster oocytes conserved their ability to support human sperm head de
condensation and male pronuclear formation following freezing-thawing.