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| Registros recuperados : 5 | |
| 1. |  | PINHEIRO, J. B. S.; SOUZA-FABJAN, J. M. G.; CORREIA, L. F. L.; OLIVEIRA, M. E. F.; FONSECA, J. F. da. Differences between 5- and 6-day progestogen-based oestrus induction protocol in Saanen and Toggenburg goats. Reproduction, Fertility, and Development, v. 33, n. 2, p. 166, 2021. Edição dos Proceedings of the 47th Annual Conference of the International Embryo Technology (IETS) Virtual Meeting, January 18-21, 2021.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 2. | | SOUZA-FABJANA, J. M. G.; BATISTA, R. I. T. P.; CORREIA, L. F. L; PARAMIO, M. T.; FONSECA, J. F. da; FREITAS, V. J. F.; MERMILLOD, P. In vitro production of small ruminant embryos: latest improvements and further research. Reproduction, Fertility and Development, v. 33, n. 2, p. 31-54, Jan. 2021.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 3. | | BRAIR, V. L.; MAIA, A. L. R. S.; CORREIA, L. F. L.; BARBOSA, N. O.; SANTOS, J. D. R.; BRANDÃO, F. Z.; FONSECA, J. F. da; BATISTA, R. I. T. P.; SOUZA-FABJAN, J. M. G. Gene expression patterns of in vivo-derived sheep blastocysts is more affected by vitrification than slow freezing technique. Cryobiology, v. 95, p. 110-115, 2020.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 4. | | MAIA, A. L. R. S.; ARRAIS, A. M.; PRELLWITZ, L.; BATISTA, R. I. T. P.; FIGUEIRA, L. M.; CORREIA, L. F. L.; FONSECA, J. F. da; SOUZA-FABJAN, J. M. G. Embryo development is impaired in goats that are treated for hydrometra and subsequently subjected to superovulation. Veterinary Record, v. 187, n. 10, e88, Aug. 2020.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 5. | | BRAIR, V. L.; MAIA, A. L. R. e S.; CORREIA, L. F. L.; PRELLWITZ, L.; PAULA, C. J. C. de; SANTOS, J. D. R.; BRANDÃO, F. Z.; FONSECA, J. F. da; BATISTA, R. I. T. P.; SOUZA-FABJAN, J. M. G. de. Vitrification technique improves more alterations on gene expression of in vivo-derived sheep blastocysts than slow freezing. Animal Reproduction, v. 17, n. 3, 2020. Edição dos Abstracts of the 34nd Annual Meeting of the Brazilian Embryo Technology Society (SBTE), 2020 (online).| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| Registros recuperados : 5 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Caprinos e Ovinos. Para informações adicionais entre em contato com cnpc.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Caprinos e Ovinos. |
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Data corrente: |
03/08/2020 |
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Data da última atualização: |
03/08/2020 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 2 |
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Autoria: |
BRAIR, V. L.; MAIA, A. L. R. S.; CORREIA, L. F. L.; BARBOSA, N. O.; SANTOS, J. D. R.; BRANDÃO, F. Z.; FONSECA, J. F. da; BATISTA, R. I. T. P.; SOUZA-FABJAN, J. M. G. |
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Afiliação: |
VIVIANE L. BRAIR, Universidade Federal Fluminense (UFF) - Niterói, RJ, Brazil; ANA LUCIA R. S. MAIA, Universidade Federal Fluminense (UFF) - Niterói, RJ, Brazil; LUCAS FRANCISCO L. CORREIA, Universidade Federal Fluminense (UFF) - Niterói, RJ, Brazil; NATHALIA O. BARBOSA, Universidade Federal Fluminense (UFF) - Niterói, RJ, Brazil; JULIANA D. R. SANTOS, Universidade Federal Fluminense (UFF) - Niterói, RJ, Brazil; FELIPE Z. BRANDÃO, Universidade Federal Fluminense (UFF) - Niterói, RJ, Brazil; JEFERSON FERREIRA DA FONSECA, CNPC; RIBRIO IVAN T. P. BATISTA, Universidade Federal Fluminense (UFF) - Niterói, RJ, Brazil; JOANNA M. G. SOUZA-FABJAN, Universidade Federal Fluminense (UFF) - Niterói, RJ, Brazil. |
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Título: |
Gene expression patterns of in vivo-derived sheep blastocysts is more affected by vitrification than slow freezing technique. |
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Ano de publicação: |
2020 |
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Fonte/Imprenta: |
Cryobiology, v. 95, p. 110-115, 2020. |
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DOI: |
https://doi.org/10.1016/j.cryobiol.2020.05.009 |
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Idioma: |
Inglês |
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Conteúdo: |
Transfer of fresh sheep embryos frequently results in higher pregnancy rate compared to cryopreserved ones, possibly due to a failure in the communication between the cryopreserved embryo and the endometrium during pre-implantation and pregnancy establishment. Thus, this study assessed the effect of sheep embryo cryopres-ervation (slow freezing or vitrification) on embryo survival rate and expression of genes related to trophectoderm differentiation (CDX2), pluripotency maintenance (NANOG), cell proliferation (TGFB1), mitochondrial activity (NRF1) and apoptosis (BAX and BCL2). Superovulation (n ¼32 ewes) was performed and embryos were transcervically collected. One hundred good quality (Grade I and II) embryos were allocated into three groups: fresh embryos (CTL; n ¼15), slow freezing (SF; n ¼42) or vitrification (VT; n ¼43). After thawing/warming, three pools of five blastocysts per group were used for RT-qPCR; the remaining 55 embryos were cultured in vitro in SOFaa medium at 38.5 �C and 5% CO2 (SF: n ¼27 and VT: n ¼28). Survival rate of SF and VT were, respectively, 29.6% (8/27) and 14.2% (4/28) at 24 h; and 48.1% (13/27) and 32.1% (9/28) at 48 h (P >0.05). Only CDX2 was affected (up-regulated, P <0.05) in both groups compared to CTL. The BAX transcript was upregulated in VT, compared to SF group. The VT increased (P <0.05) the expression of all genes, except for NANOG and NRF1, when compared to the CTL. In conclusion, although in vitro survival was similar between techniques, VT led to increased changes in blastocyst gene expression compared to CTL and SF. MenosTransfer of fresh sheep embryos frequently results in higher pregnancy rate compared to cryopreserved ones, possibly due to a failure in the communication between the cryopreserved embryo and the endometrium during pre-implantation and pregnancy establishment. Thus, this study assessed the effect of sheep embryo cryopres-ervation (slow freezing or vitrification) on embryo survival rate and expression of genes related to trophectoderm differentiation (CDX2), pluripotency maintenance (NANOG), cell proliferation (TGFB1), mitochondrial activity (NRF1) and apoptosis (BAX and BCL2). Superovulation (n ¼32 ewes) was performed and embryos were transcervically collected. One hundred good quality (Grade I and II) embryos were allocated into three groups: fresh embryos (CTL; n ¼15), slow freezing (SF; n ¼42) or vitrification (VT; n ¼43). After thawing/warming, three pools of five blastocysts per group were used for RT-qPCR; the remaining 55 embryos were cultured in vitro in SOFaa medium at 38.5 �C and 5% CO2 (SF: n ¼27 and VT: n ¼28). Survival rate of SF and VT were, respectively, 29.6% (8/27) and 14.2% (4/28) at 24 h; and 48.1% (13/27) and 32.1% (9/28) at 48 h (P >0.05). Only CDX2 was affected (up-regulated, P <0.05) in both groups compared to CTL. The BAX transcript was upregulated in VT, compared to SF group. The VT increased (P <0.05) the expression of all genes, except for NANOG and NRF1, when compared to the CTL. In conclusion, although in vitro survival was similar between... Mostrar Tudo |
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Palavras-Chave: |
Apoptosis regulator; Embryo cryopreservation; Embryonic metabolism; Reproductive biotechnologies. |
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Thesaurus NAL: |
Embryo implantation; Embryo transfer; Ewes. |
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Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
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Marc: |
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024 7 $ahttps://doi.org/10.1016/j.cryobiol.2020.05.009$2DOI
100 1 $aBRAIR, V. L.
245 $aGene expression patterns of in vivo-derived sheep blastocysts is more affected by vitrification than slow freezing technique.$h[electronic resource]
260 $c2020
520 $aTransfer of fresh sheep embryos frequently results in higher pregnancy rate compared to cryopreserved ones, possibly due to a failure in the communication between the cryopreserved embryo and the endometrium during pre-implantation and pregnancy establishment. Thus, this study assessed the effect of sheep embryo cryopres-ervation (slow freezing or vitrification) on embryo survival rate and expression of genes related to trophectoderm differentiation (CDX2), pluripotency maintenance (NANOG), cell proliferation (TGFB1), mitochondrial activity (NRF1) and apoptosis (BAX and BCL2). Superovulation (n ¼32 ewes) was performed and embryos were transcervically collected. One hundred good quality (Grade I and II) embryos were allocated into three groups: fresh embryos (CTL; n ¼15), slow freezing (SF; n ¼42) or vitrification (VT; n ¼43). After thawing/warming, three pools of five blastocysts per group were used for RT-qPCR; the remaining 55 embryos were cultured in vitro in SOFaa medium at 38.5 �C and 5% CO2 (SF: n ¼27 and VT: n ¼28). Survival rate of SF and VT were, respectively, 29.6% (8/27) and 14.2% (4/28) at 24 h; and 48.1% (13/27) and 32.1% (9/28) at 48 h (P >0.05). Only CDX2 was affected (up-regulated, P <0.05) in both groups compared to CTL. The BAX transcript was upregulated in VT, compared to SF group. The VT increased (P <0.05) the expression of all genes, except for NANOG and NRF1, when compared to the CTL. In conclusion, although in vitro survival was similar between techniques, VT led to increased changes in blastocyst gene expression compared to CTL and SF.
650 $aEmbryo implantation
650 $aEmbryo transfer
650 $aEwes
653 $aApoptosis regulator
653 $aEmbryo cryopreservation
653 $aEmbryonic metabolism
653 $aReproductive biotechnologies
700 1 $aMAIA, A. L. R. S.
700 1 $aCORREIA, L. F. L.
700 1 $aBARBOSA, N. O.
700 1 $aSANTOS, J. D. R.
700 1 $aBRANDÃO, F. Z.
700 1 $aFONSECA, J. F. da
700 1 $aBATISTA, R. I. T. P.
700 1 $aSOUZA-FABJAN, J. M. G.
773 $tCryobiology$gv. 95, p. 110-115, 2020.
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