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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/14644
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dc.contributor.authorGreen, R. E.-
dc.contributor.authorSantos, B. F. S.-
dc.contributor.authorSicherle, C. C.-
dc.contributor.authorLandim-Alvarenga, Fernanda da Cruz-
dc.contributor.authorBicudo, Sony Dimas-
dc.date.accessioned2013-09-30T18:28:48Z-
dc.date.accessioned2014-05-20T13:42:08Z-
dc.date.accessioned2016-10-25T16:57:02Z-
dc.date.available2013-09-30T18:28:48Z-
dc.date.available2014-05-20T13:42:08Z-
dc.date.available2016-10-25T16:57:02Z-
dc.date.issued2009-06-01-
dc.identifierhttp://dx.doi.org/10.1111/j.1439-0531.2008.01088.x-
dc.identifier.citationReproduction In Domestic Animals. Malden: Wiley-blackwell Publishing, Inc, v. 44, n. 3, p. 406-410, 2009.-
dc.identifier.issn0936-6768-
dc.identifier.urihttp://hdl.handle.net/11449/14644-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/14644-
dc.description.abstractThe aim of this study was to evaluate the viability in the effect of open pulled straw (OPS) vitrification procedure of sheep embryos after direct transference. Embryos were produced in vivo and cryopreserved in slow freezing or OPS vitrification. The survival rates of cryopreserved embryos were compared to non-frozen standard pattern. In a first set of experiments, embryos at morula and blastocyst stages were dived in ethylene glycol (1.5 M) and frozen in an automatic freezer. After being thawed, they were directly or indirectly transferred to ewes recipient. A second group of embryos were drawn into OPS and plunged into liquid nitrogen after being exposed at room temperature for 1 min and 45 s in 10% EG plus 10% dimethyl sulphoxide (DMSO), then again for 30 s in 20% EG + 20% DMSO + 0.5 M sucrose. After being warmed, embryos were also directly transferred using a French mini straw as the catheter for the transplantation process or after in vitro dilution of cryoprotectants (two-step-process). No significant difference was observed among fresh, frozen or vitrified embryos on pregnancy rate (50.0%, 38.6% and 55.8%). However, when we evaluated only the direct transference, the pregnancy rate of OPS vitrified embryos was higher than that of frozen embryos (57.1% vs 34.8%) (p = 0.07). In addition, vitrified morulae had a higher pregnancy rate than the one with frozen embryos (64.0% vs 38.9%) (p = 0.07). Finally, our results indicate that OPS vitrification technique in association with direct transference improves the viability of sheep embryos with potential applications to field conditions.en
dc.format.extent406-410-
dc.language.isoeng-
dc.publisherWiley-Blackwell Publishing, Inc-
dc.sourceWeb of Science-
dc.titleViability of OPS Vitrified Sheep Embryos After Direct Transferen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationVet Med & Anim Sci Univ, Dept Vet Reprod & Radiol, UNESP, Fac Vet Med & Anim Sci, BR-18618000 Botucatu, SP, Brazil-
dc.description.affiliationUnespVet Med & Anim Sci Univ, Dept Vet Reprod & Radiol, UNESP, Fac Vet Med & Anim Sci, BR-18618000 Botucatu, SP, Brazil-
dc.identifier.doi10.1111/j.1439-0531.2008.01088.x-
dc.identifier.wosWOS:000266031500008-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofReproduction in Domestic Animals-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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