1993Journal of Reproduction and DevelopmentOpen access

Stage-Dependent Viability of Mouse Preimplantation Embryos Vitrified with Sugar-containing Solutions.

Norihiro Tada, Masahiro Sato, Egon Amann, Shyoso OGAWA

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Abstract

The aim of the work is to determine the susceptibility of mouse preimplantation embryos to vitrification at different developmental stages. The experiment was carried out in embryos at 1-cell, morula and blastocyst stages. As a vitrification solution, a mixture of 2.5 M dimethylsulphoxide + 2.5 M propylene glycol (DP), DP + 1.0 M sucrose (DPS) or DP + 0.16 M raffinose (DPR), was used. The in vitro survival, evaluated by the development into a late blastocyst stage in vitro, of control and vitrified mouse embryos was examined. A high survival rate (80%) after vitrification was obtained for 1-cell embryos after a 15 sec-exposure to DPS. High survival rates for morulae (91-96%) and relatively low survival rates for blastocysts (30-55%) were observed after vitrification in either DPS or DPR after short exposures (within 30 sec). In vivo survival rate for each embryos vitrified in DPS by a short exposure (within 30 sec) at 1-cell, morula or blastocyst stage was 56, 53 or 40%. Though the rates for 1-cell and molura stages were comparable with those in control embryos (55 and 58%), the rate for blastocyst stage was significantly lower (P<0.05) than that in control embryos (56%). Thus, the proposed vitrification procedure can be useful in the cryopreservation of mouse preimplantation embryos at 1-cell and morula stages.

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What this paper is about

The aim of the work is to determine the susceptibility of mouse preimplantation embryos to vitrification at different developmental stages. The experiment was carried out in embryos at 1-cell, morula and blastocyst stages. As a vitrification solution, a mixture of 2.5 M dimethylsulphoxide + 2.5 M propylene glycol (DP), DP + 1.0 M sucrose (DPS) or DP + 0.16 M raffinose (DPR), was used. The in vitro survival, evaluated by the development into a late blastocyst stage in vitro, of control and vitrified mouse embryos was examined. A high survival rate (80%) after vitrification was obtained for 1-cell embryos after a 15 sec-exposure to DPS. High survival rates for morulae (91-96%) and relatively low survival rates for blastocysts (30-55%) were observed after vitrification in either DPS or DPR after short exposures (within 30 sec). In vivo survival rate for each embryos vitrified in DPS by a short exposure (within 30 sec) at 1-cell, morula or blastocyst stage was 56, 53 or 40%. Though the rates for 1-cell and molura stages were comparable with those in control embryos (55 and 58%), the rate for blastocyst stage was significantly lower (P<0.05) than that in control embryos (56%). Thus, the proposed vitrification procedure can be useful in the cryopreservation of mouse preimplantation embryos at 1-cell and morula stages.

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Available abstract

The aim of the work is to determine the susceptibility of mouse preimplantation embryos to vitrification at different developmental stages. The experiment was carried out in embryos at 1-cell, morula and blastocyst stages. As a vitrification solution, a mixture of 2.5 M dimethylsulphoxide + 2.5 M propylene glycol (DP), DP + 1.0 M sucrose (DPS) or DP + 0.16 M raffinose (DPR), was used. The in vitro survival, evaluated by the development into a late blastocyst stage in vitro, of control and vitrified mouse embryos was examined. A high survival rate (80%) after vitrification was obtained for 1-cell embryos after a 15 sec-exposure to DPS. High survival rates for morulae (91-96%) and relatively low survival rates for blastocysts (30-55%) were observed after vitrification in either DPS or DPR after short exposures (within 30 sec). In vivo survival rate for each embryos vitrified in DPS by a short exposure (within 30 sec) at 1-cell, morula or blastocyst stage was 56, 53 or 40%. Though the rates for 1-cell and molura stages were comparable with those in control embryos (55 and 58%), the rate for blastocyst stage was significantly lower (P<0.05) than that in control embryos (56%). Thus, the proposed vitrification procedure can be useful in the cryopreservation of mouse preimplantation embryos at 1-cell and morula stages.

Key concepts: Vitrification, Blastocyst, Andrology, Embryo, Cryopreservation, Biology, Embryo cryopreservation, Survival rate

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