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Registros recuperados : 12 | |
1. |  | MARINHO, L. R. S.; CASALI, R.; DRUM, J. N.; ZAGO, F. C.; MEZZALIRA, J. C.; FORELL, F.; MEZZALIRA, A. Toxidade do etanol a 0,1% no cultivo de embriões bovinos produzidos in vitro. In: SEMINÁRIO REGIONAL DOS PÓS-GRADUANDOS EM CIÊNCIAS AGRÁRIAS, 3., 2010, Lages, SC. Anais... Lages: UDESC, 2010. Biblioteca(s): Epagri-Sede. |
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2. |  | TRINDADE, J.; NEVES, F. P.; PINTO, C. E.; BREMM, C.; MEZZALIRA, J. C.; NADIN, L. B.; GENRO, T. C. M.; GONDA, H. L.; CARVALHO, P. C. F. Daily Forage Intake by Cattle on Natural Grassland: Response to Forage Allowance and Sward Structure. Rangeland Ecology & Management, Davis, CA, USA, v. 69, n. 1, p. 59-67, 2016. Biblioteca(s): Epagri-Sede. |
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3. |  | SOARES, A. B.; CARVALHO, P. C. de F.; NABINGER, C.; TRINDADE, J. P. P.; TRINDADE, J. K. da; MEZZALIRA, J. C. Dinâmica da composição botânica numa pastagem natural sob efeito de diferentes ofertas de forragem. Ciência Rural, Santa Maria, v. 41, n. 8., p. 1459-1465, ago. 2011. Biblioteca(s): Epagri-Sede. |
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4. |  | MEZZALIRA, J. C.; PINTO, M. G. L.; ZAGO, F. C.; SILVA, A. M.; ALBINO, N.; KLEIN, N.; BORDIGNON, V.; OHLWEILER, L. U.; MEZZALIRA, A. Prenancy of cloned embryos a freemartin cow and endangered breed. In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA DE TECNOLOGIA DE EMBRIÕES, 25., 2011, Cumbuco, CE. [Anais...]. Porto Alegre, RS: UFRGS, 2011. p. 444. Biblioteca(s): Epagri-Sede. |
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5. |  | MEZZALIRA, J. C.; OHLWEILER, L. U.; URIO, M.; GAUDENCIO NETO, S.; MARINHO, L. R. S.; ZAGO, F. C.; FORELL, F.; BERTOLINI, M.; MEZZALIRA, A. Effect of nitrocooler negative pressure and recovery internal on cryotolerance of bovine in vitroproduced embryos. In: ANNUAL CONFERECE OF IETS, ., 2010, Cordoba, Argentina. Proceedings... Sydney, Australia: CSIRO, 2010. p. 210. Biblioteca(s): Epagri-Sede. |
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6. |  | MACHADO JR., J.; URIO, M.; AGUIAR, L. H. de; FORELL, F.; FRAJBLAT, M.; OHLWEILER, L. U.; MEZZALIRA, J. C.; MEZZALIRA, A. Mice embryos cryopreservation: Vitrification or ultra-Rapid freezing? Acta Scientiae Veterinariae, Porto Alegre, RS, v. 38, n. 3/4, p. 357-362, 2010. Biblioteca(s): Epagri-Sede. |
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7. |  | MEZZALIRA, J. C.; CARVALHO, P. C. de F.; TRINDADE, J. K. da; BREMM, C.; FONSECA, L.; AMARAL, M. F. do; REFFATTI, M. V. Produção animal e vegetal em pastagem nativa manejada sob diferentes ofertas de forragem por bovinos. Ciência Rural, Santa Maria, v. 42, n. 7, p. 1264-1270, jul. 2012. Biblioteca(s): Epagri-Sede. |
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8. |  | SANTOS, R. M. dos; BARRETA, M. H.; FRAJBLAT, M.; CUCCO, D. C.; MEZZALIRA, J. C.; BUNN, S.; CRUZ, F. B.; VIEIRA, A. D.; MEZZALIRA, A. Vacuum-cooled liquid nitrogen increases the developmental ability of vitrified-warmed bovine oocytes. Ciencia Rural, Santa Maria, v. 36, n. 5, p. 1501-1506, set./out. 2006. Biblioteca(s): Epagri-Sede. |
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9. |  | TRINDADE, J.; PINTO, C. E.; NEVES, F. P.; MEZZALIRA, J. C.; BREMM, C.; GENRO, T. C. M.; TISCHLER, M. R.; NABINGER, C.; GONDA, H. L.; CARVALHO, P. C. F. Forage Allowance as a Target of Grazing Management: Implications on Grazing Time and Forage Searching. Rangeland Ecology & Management, Littleton, Colorado, USA, v. 65, n. 4, p. 382-393, 2012. Biblioteca(s): Epagri-Sede. |
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10. |  | GERGER, R. P. C.; FORELL, F.; MEZZALIRA, J. C.; ZAGO, F. C.; VIEIRA, F. K.; MACHADO JÚNIOR, J.; OHLWEILER, L. U.; RAUBER, L. P.; RODRIGUES, J. L. R.; AMBRÓSIO, C. E.; MIGLINO, M. A.; MEZZALIRA, A.; BERTOLINI, M. Effect of Fusion-Activation Interval and Embryo Aggregation on In Vitro and In Vivo Development of Cloned Bovine Embryos Produced by Handmade Cloning. In: ANNUAL CONFERENCE OF IETS, 2010, Córdoba, Argentina. Proceedings... Sydney, Austrália: Csiro, 2010. p. 185-186. Biblioteca(s): Epagri-Sede. |
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11. |  | CARVALHO, P. C. F.; MEZZALIRA, J. C.; FONSECA, L.; WESP, C. L.; TRINDADE, J. K.; NEVES, F. P.; PINTO, C. E.; AMARAL, M. F.; BREMM, C.; AMARAL, G. A.; SANTOS, D. T.; CHOPA, F. S.; GONDA, H.; NABINGER, C.; POLI, C. H. E. C. Do bocado ao sitio de pastejo: manejo em 3D para compatibilizar a estrutura do pasto e o processo de pastejo. In: SIMPÓSIO DE FORRAGICULTURA, 7. CONGRESSO DE FORRAGICULTURA E PASTAGENS, 3., 2009, Lavras, MG. [Anais...]. Lavras, MG: UFLA, 2009. p. 175-198. Biblioteca(s): Epagri-Sede. |
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12. |  | ORTIGARI JÚNIOR, I.; GERGER, R. P. C.; RIBEIRO, E. S.; MEZZALIRA, J. C.; ZAGO, F. C.; GAUDÊNCIO NETO, S.; OHLWEILER, L. U.; MARTINS, L. T.; BERTOLINI, L. R.; FORELL, F.; COSTA, U. M.; LOPES, R. F. F.; RODRIGUES, J. L.; AMBRÓSIO, C. E.; MIGLINO, M. A.; MEZZALIRA, A.; BERTOLINI, M. Efeito da evolução técnica na eficiência na clonagem por handmade cloning em bovinos. In: REUNIÃO ANUAL DA SOCIEDADE BRASILERIA DE TECNOLOGIA DE EMBRIÕES, 24., 2010, Porto de Galinhas, PE. Anais... Porto Alegre, RS: UFRGS, 2010. p. 803. Biblioteca(s): Epagri-Sede. |
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Registros recuperados : 12 | |
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Registro Completo
Biblioteca(s): |
Epagri-Sede. |
Data corrente: |
10/08/2011 |
Data da última atualização: |
10/08/2011 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Circulação/Nível: |
-- - -- |
Autoria: |
MEZZALIRA, J. C.; OHLWEILER, L. U.; URIO, M.; GAUDENCIO NETO, S.; MARINHO, L. R. S.; ZAGO, F. C.; FORELL, F.; BERTOLINI, M.; MEZZALIRA, A. |
Afiliação: |
Epagri |
Título: |
Effect of nitrocooler negative pressure and recovery internal on cryotolerance of bovine in vitroproduced embryos. |
Ano de publicação: |
2010 |
Fonte/Imprenta: |
In: ANNUAL CONFERECE OF IETS, ., 2010, Cordoba, Argentina. Proceedings... Sydney, Australia: CSIRO, 2010. p. 210. |
Idioma: |
Inglês |
Conteúdo: |
Exposing bovine embryos and porcine oocytes to hydrostatic pressure has been shown to increase cryosurvival, possibly by a resulting expression of stress tolerance proteins. This study aimed to evaluate the effect of the negative pressure stress condition (a 5¨Cmin long embryo exposure to a negative pressure,) and the interval between vacuum exposure and vitrification (40 min or 2 h) on survival of bovine IVP embryos. The negative pressure was achieved with the same apparatus used previously for the cryopreservation of embryos (¡ä¡äNitrocooler¡ä¡ä; Mezzalira et al. 2009 Reprod Fert Dev (1) 134), in which a negative pressure (vacuum) is applied to liquid nitrogen to increase the cooling rate through the slush phenomenon, except that, in this study, the vacuum was applied to the chamber without liquid nitrogen, at room temperature. Grades 1 and 2 bovine IVP expanded blastocysts were allocated to one of five experimental groups: embryos in vitro-cultured as fresh (Control) or after vitrification (Vitri); and embryos subjected to the negative pressure for 5 min and then in vitro¨Ccultured as fresh (NP¨Cfresh) or after vitrification performed 40 min (NP¨CVitri¨C40min) or 2 h (NP-Vitri-2h) following the vacuum exposure. Embryos were vitrified in pulled glass micropipettes in a solution with 20% ethylene glycol + 20% dimethylsulfoxide + 20% fetal bovine serum and rewarmed in decreasing sucrose concentrations (Mezzalira et al. 1999 Acta Scientiae Veterinariae (27) 262¨C262). In vitro culture was carried out in all treatments for 72 h for the assessment of re¨Cexpansion and hatching rates, which were analyzed by the chi¨Csquare test, for P<0.05. No differences in re¨Cexpansion rates were observed between groups. However, the vitrification of embryos after 2 h of exposure to a 5¨Cmin long negative pressure (NP¨CVitri¨C2h) improved embryo survival expressed by a higher hatching rate than for embryos vitrified without vacuum exposure (Vitri) or after 40 min following the 5¨Cmin long exposure to vacuum. In addition, hatching rates in group NP¨CVitri¨C2h was similar to those for fresh embryos (Control and NP¨Cfresh). Our results indicated that a short exposure of embryos to a negative pressure can improve cryotolerance following vitrification, which is dependent on the time interval between NP exposure and cryopreservation. Bovine IVP embryos should be allowed to recover for at least two hours after NP exposure before the increase in cryotolerance is achieved. MenosExposing bovine embryos and porcine oocytes to hydrostatic pressure has been shown to increase cryosurvival, possibly by a resulting expression of stress tolerance proteins. This study aimed to evaluate the effect of the negative pressure stress condition (a 5¨Cmin long embryo exposure to a negative pressure,) and the interval between vacuum exposure and vitrification (40 min or 2 h) on survival of bovine IVP embryos. The negative pressure was achieved with the same apparatus used previously for the cryopreservation of embryos (¡ä¡äNitrocooler¡ä¡ä; Mezzalira et al. 2009 Reprod Fert Dev (1) 134), in which a negative pressure (vacuum) is applied to liquid nitrogen to increase the cooling rate through the slush phenomenon, except that, in this study, the vacuum was applied to the chamber without liquid nitrogen, at room temperature. Grades 1 and 2 bovine IVP expanded blastocysts were allocated to one of five experimental groups: embryos in vitro-cultured as fresh (Control) or after vitrification (Vitri); and embryos subjected to the negative pressure for 5 min and then in vitro¨Ccultured as fresh (NP¨Cfresh) or after vitrification performed 40 min (NP¨CVitri¨C40min) or 2 h (NP-Vitri-2h) following the vacuum exposure. Embryos were vitrified in pulled glass micropipettes in a solution with 20% ethylene glycol + 20% dimethylsulfoxide + 20% fetal bovine serum and rewarmed in decreasing sucrose concentrations (Mezzalira et al. 1999 Acta Scientiae Veterinariae (27) 262¨C262). In vitr... Mostrar Tudo |
Palavras-Chave: |
Bovine; Cryotolerance; Embryos; Nitrocooler; Pressure. |
Categoria do assunto: |
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Marc: |
LEADER 03090naa a2200181 a 4500 001 1079201 005 2011-08-10 008 2010 bl uuuu u00u1 u #d 100 1 $aEpagri 245 $aEffect of nitrocooler negative pressure and recovery internal on cryotolerance of bovine in vitroproduced embryos. 260 $c2010 520 $aExposing bovine embryos and porcine oocytes to hydrostatic pressure has been shown to increase cryosurvival, possibly by a resulting expression of stress tolerance proteins. This study aimed to evaluate the effect of the negative pressure stress condition (a 5¨Cmin long embryo exposure to a negative pressure,) and the interval between vacuum exposure and vitrification (40 min or 2 h) on survival of bovine IVP embryos. The negative pressure was achieved with the same apparatus used previously for the cryopreservation of embryos (¡ä¡äNitrocooler¡ä¡ä; Mezzalira et al. 2009 Reprod Fert Dev (1) 134), in which a negative pressure (vacuum) is applied to liquid nitrogen to increase the cooling rate through the slush phenomenon, except that, in this study, the vacuum was applied to the chamber without liquid nitrogen, at room temperature. Grades 1 and 2 bovine IVP expanded blastocysts were allocated to one of five experimental groups: embryos in vitro-cultured as fresh (Control) or after vitrification (Vitri); and embryos subjected to the negative pressure for 5 min and then in vitro¨Ccultured as fresh (NP¨Cfresh) or after vitrification performed 40 min (NP¨CVitri¨C40min) or 2 h (NP-Vitri-2h) following the vacuum exposure. Embryos were vitrified in pulled glass micropipettes in a solution with 20% ethylene glycol + 20% dimethylsulfoxide + 20% fetal bovine serum and rewarmed in decreasing sucrose concentrations (Mezzalira et al. 1999 Acta Scientiae Veterinariae (27) 262¨C262). In vitro culture was carried out in all treatments for 72 h for the assessment of re¨Cexpansion and hatching rates, which were analyzed by the chi¨Csquare test, for P<0.05. No differences in re¨Cexpansion rates were observed between groups. However, the vitrification of embryos after 2 h of exposure to a 5¨Cmin long negative pressure (NP¨CVitri¨C2h) improved embryo survival expressed by a higher hatching rate than for embryos vitrified without vacuum exposure (Vitri) or after 40 min following the 5¨Cmin long exposure to vacuum. In addition, hatching rates in group NP¨CVitri¨C2h was similar to those for fresh embryos (Control and NP¨Cfresh). Our results indicated that a short exposure of embryos to a negative pressure can improve cryotolerance following vitrification, which is dependent on the time interval between NP exposure and cryopreservation. Bovine IVP embryos should be allowed to recover for at least two hours after NP exposure before the increase in cryotolerance is achieved. 653 $aBovine 653 $aCryotolerance 653 $aEmbryos 653 $aNitrocooler 653 $aPressure 773 $tIn: ANNUAL CONFERECE OF IETS, ., 2010, Cordoba, Argentina. Proceedings... Sydney, Australia: CSIRO, 2010. p. 210.
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