2013Journal of Jiangsu UniversityRequires access

Effects of vitrifying mouse embryos from different periods and different sources

Jiabo Hu

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Abstract

Objective: To compare the post-thaw survival rate and the success rate in continuing to grow to blastocyst of vitrified mouse embryos from different periods and different sources.Methods: The 2-cell,4-cell,8-cell period mouse embryos were obtained through fertilization in vitro and in vivo respectively.These embryos were vitrified and thawed.We got the rate of their survival and blastocyst formation.And,we took those fresh embryos as the control group.Results: The survival rate of blastocyst formation of post-thaw 2-cell,4-cell and 8-cell period embryos from fertilization in vitro and in vivo were 70.67%/65.33% and 72.06%/67.62%,88.00%/81.33% and 89.71%/83.82% and 93.33%/92.00% and 94.12%/94.12% respectively.The blastocyst formation rate in the phrase of 2-cell and 4-cell frozen embryos was lower than the control group(P0.05).No significant difference was found between the group of 8-cell frozen embryos and the control group.In addition,fertilization modes had no significant effect on the survival rate and the blastocyst formation rate(P0.05).Conclusion: Vitrification technology is an effective method in preserving mouse embryos.And the 8-cell period embryos might have the best cryopreservation effect.

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Objective: To compare the post-thaw survival rate and the success rate in continuing to grow to blastocyst of vitrified mouse embryos from different periods and different sources.Methods: The 2-cell,4-cell,8-cell period mouse embryos were obtained through fertilization in vitro and in vivo respectively.These embryos were vitrified and thawed.We got the rate of their survival and blastocyst formation.And,we took those fresh embryos as the control group.Results: The survival rate of blastocyst formation of post-thaw 2-cell,4-cell and 8-cell period embryos from fertilization in vitro and in vivo were 70.67%/65.33% and 72.06%/67.62%,88.00%/81.33% and 89.71%/83.82% and 93.33%/92.00% and 94.12%/94.12% respectively.The blastocyst formation rate in the phrase of 2-cell and 4-cell frozen embryos was lower than the control group(P0.05).No significant difference was found between the group of 8-cell frozen embryos and the control group.In addition,fertilization modes had no significant effect on the survival rate and the blastocyst formation rate(P0.05).Conclusion: Vitrification technology is an effective method in preserving mouse embryos.And the 8-cell period embryos might have the best cryopreservation effect.

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Available abstract

Objective: To compare the post-thaw survival rate and the success rate in continuing to grow to blastocyst of vitrified mouse embryos from different periods and different sources.Methods: The 2-cell,4-cell,8-cell period mouse embryos were obtained through fertilization in vitro and in vivo respectively.These embryos were vitrified and thawed.We got the rate of their survival and blastocyst formation.And,we took those fresh embryos as the control group.Results: The survival rate of blastocyst formation of post-thaw 2-cell,4-cell and 8-cell period embryos from fertilization in vitro and in vivo were 70.67%/65.33% and 72.06%/67.62%,88.00%/81.33% and 89.71%/83.82% and 93.33%/92.00% and 94.12%/94.12% respectively.The blastocyst formation rate in the phrase of 2-cell and 4-cell frozen embryos was lower than the control group(P0.05).No significant difference was found between the group of 8-cell frozen embryos and the control group.In addition,fertilization modes had no significant effect on the survival rate and the blastocyst formation rate(P0.05).Conclusion: Vitrification technology is an effective method in preserving mouse embryos.And the 8-cell period embryos might have the best cryopreservation effect.

Key concepts: Blastocyst, Andrology, Embryo, Vitrification, Cryopreservation, Human fertilization, Biology, Embryo cryopreservation

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