The purpose of this study was to evaluate the viability and subsequent developmental ability of porcine germinal vesicle（GV） oocytes vitrified step-wise exposure to cryoprotectants. Oocytes were transferred to a vit...The purpose of this study was to evaluate the viability and subsequent developmental ability of porcine germinal vesicle（GV） oocytes vitrified step-wise exposure to cryoprotectants. Oocytes were transferred to a vitrification solution composed of 10% ethylene glycol（EG）,10% dimethyl sulfoxide（DMSO）, 300 g/L-1 Ficoll and 0.5 mol/L-1 sucrose（EDFS40） in a direct manner （non-preequilibrium） or in step-wise manner（ single- and two-step preequilibrium）. After vitrification and storage in liquid nitrogen, the oocytes were thawed,washed and in vitro maturation, fertilization and culture. In the non-preequilibrium group, the rates of post-thawed oocytes surviving, maturing to metaphase-Ⅱ, cleavage rate and blastocysts rate was significantly lower than that of sigle- and two-step preequilubrium groups（P<0.05）. In the single- and two- step groups, the rates of metaphase-Ⅱ stage were 46.8%, 42.7% and 49.7%, respectively, the rates which developed to blastocysts were 10.5%,11.1% and 14.8%, respectivaly. In the non-vitrified control group,the rates of oocytes maturing to metaphase-Ⅱ, developing to blastocysts was significantly higher than that vitrified groups（P<0.05）. The present study shows that the vitrification of porcine GV oocytes by a step-wise method involving two-steps preequilibrium may have advantage in maintaining the viability and subsequent production of blastocysts.展开更多
基金Item supported by international coopera-tion programme of science and technology of Shanghai (No.015407005)
文摘The purpose of this study was to evaluate the viability and subsequent developmental ability of porcine germinal vesicle（GV） oocytes vitrified step-wise exposure to cryoprotectants. Oocytes were transferred to a vitrification solution composed of 10% ethylene glycol（EG）,10% dimethyl sulfoxide（DMSO）, 300 g/L-1 Ficoll and 0.5 mol/L-1 sucrose（EDFS40） in a direct manner （non-preequilibrium） or in step-wise manner（ single- and two-step preequilibrium）. After vitrification and storage in liquid nitrogen, the oocytes were thawed,washed and in vitro maturation, fertilization and culture. In the non-preequilibrium group, the rates of post-thawed oocytes surviving, maturing to metaphase-Ⅱ, cleavage rate and blastocysts rate was significantly lower than that of sigle- and two-step preequilubrium groups（P<0.05）. In the single- and two- step groups, the rates of metaphase-Ⅱ stage were 46.8%, 42.7% and 49.7%, respectively, the rates which developed to blastocysts were 10.5%,11.1% and 14.8%, respectivaly. In the non-vitrified control group,the rates of oocytes maturing to metaphase-Ⅱ, developing to blastocysts was significantly higher than that vitrified groups（P<0.05）. The present study shows that the vitrification of porcine GV oocytes by a step-wise method involving two-steps preequilibrium may have advantage in maintaining the viability and subsequent production of blastocysts.
