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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: |
08/09/2017 |
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Data da última atualização: |
11/09/2017 |
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Autoria: |
KESKINTEPE, L.; MORTON, P. C.; SMITH, S. E.; TUCKER, M. J.; SIMPLICIO, A. A.; BRACKETT, B. G. |
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Afiliação: |
College of Veterinary Medicine, Athens, Georgia, USA, and Reproductive Biology Associates, Atlanta, Georgia, USA; CNPC. |
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Título: |
Caprine blastocyst formation following intracytoplasmic sperm injection and defined culture. |
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Ano de publicação: |
1997 |
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Fonte/Imprenta: |
Zygote, v. 5, n. 3, p. 261-265, Aug. 1997. |
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DOI: |
https://doi.org/10.1017/S0967199400003701 |
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Idioma: |
Inglês |
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Conteúdo: |
Abstract: Experiments were undertaken to develop intracytoplasmic sperm injection (ICSI) to produce caprine embryos out of the normal breeding season. Oocytes were obtained from 2?6 mm ovarian follicles at slaughter. Selected oocytes with two to four layers of cumulus cells were incubated in 1 ml of H-TCM 199 supplemented with 10 ?g each of oFSH and bLH (NHPP, NIDDK, NICHD, USDA) and 20% fetal bovine serum (FBS) in a thermos (38.5°C) for 4.5 h during transportation. Then, oocytes were transferred into 75 ?l of freshly prepared maturation medium under paraffin oil and a mixture of 5% O2, 5% CO2 and 90% N2. Approximately 26 h after recovery oocytes were denuded by incubation with hyaluronidase (100 IU/ml) and pipetting and held at 38.5°C for 90 min. Spermatozoa frozen in egg yolk extender were thawed in a 37°C water bath for 15s. Motile fractions were selected by swim-up, then incubated for 90 mm in TALP with 10 ?g heparin/ml. Each oocyte was positioned with its first polar body at 6 or 12 o'clock by a holding pipette. Sperm (1 ?l) were added to 10 ?l medium containing 10% polyvinylpyrrolidone. A sperm cell was aspirated into a pipette, and then injected head-first into the cytoplasm of an oocyte maintained in H-TCM 199 + 20% FBS at 37°C. Injected oocytes were transferred to HM and, after 90 min, cultured in 50 ?l of BSA-free synthetic oviduct fluid plus polyvinyl alcohol, citrate and non-essential amino acids. Results demonstrate that caprine blastocysts can be produced outside the breeding season by the use of frozen-thawed semen and injection of sperm cells with broken tails into ova followed by culture in defined medium. MenosAbstract: Experiments were undertaken to develop intracytoplasmic sperm injection (ICSI) to produce caprine embryos out of the normal breeding season. Oocytes were obtained from 2?6 mm ovarian follicles at slaughter. Selected oocytes with two to four layers of cumulus cells were incubated in 1 ml of H-TCM 199 supplemented with 10 ?g each of oFSH and bLH (NHPP, NIDDK, NICHD, USDA) and 20% fetal bovine serum (FBS) in a thermos (38.5°C) for 4.5 h during transportation. Then, oocytes were transferred into 75 ?l of freshly prepared maturation medium under paraffin oil and a mixture of 5% O2, 5% CO2 and 90% N2. Approximately 26 h after recovery oocytes were denuded by incubation with hyaluronidase (100 IU/ml) and pipetting and held at 38.5°C for 90 min. Spermatozoa frozen in egg yolk extender were thawed in a 37°C water bath for 15s. Motile fractions were selected by swim-up, then incubated for 90 mm in TALP with 10 ?g heparin/ml. Each oocyte was positioned with its first polar body at 6 or 12 o'clock by a holding pipette. Sperm (1 ?l) were added to 10 ?l medium containing 10% polyvinylpyrrolidone. A sperm cell was aspirated into a pipette, and then injected head-first into the cytoplasm of an oocyte maintained in H-TCM 199 + 20% FBS at 37°C. Injected oocytes were transferred to HM and, after 90 min, cultured in 50 ?l of BSA-free synthetic oviduct fluid plus polyvinyl alcohol, citrate and non-essential amino acids. Results demonstrate that caprine blastocysts can be produced outsi... Mostrar Tudo |
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Palavras-Chave: |
Animal embryos; Cleavage Stage; FSH; LH. |
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Thesagro: |
Caprino; Embrião animal. |
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Thesaurus NAL: |
Blastocystis; Goats; hyaluronoglucosaminidase; Ionophores; Pharmacology. |
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Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
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Marc: |
LEADER 02535naa a2200325 a 4500
001 2075267
005 2017-09-11
008 1997 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1017/S0967199400003701$2DOI
100 1 $aKESKINTEPE, L.
245 $aCaprine blastocyst formation following intracytoplasmic sperm injection and defined culture.
260 $c1997
520 $aAbstract: Experiments were undertaken to develop intracytoplasmic sperm injection (ICSI) to produce caprine embryos out of the normal breeding season. Oocytes were obtained from 2?6 mm ovarian follicles at slaughter. Selected oocytes with two to four layers of cumulus cells were incubated in 1 ml of H-TCM 199 supplemented with 10 ?g each of oFSH and bLH (NHPP, NIDDK, NICHD, USDA) and 20% fetal bovine serum (FBS) in a thermos (38.5°C) for 4.5 h during transportation. Then, oocytes were transferred into 75 ?l of freshly prepared maturation medium under paraffin oil and a mixture of 5% O2, 5% CO2 and 90% N2. Approximately 26 h after recovery oocytes were denuded by incubation with hyaluronidase (100 IU/ml) and pipetting and held at 38.5°C for 90 min. Spermatozoa frozen in egg yolk extender were thawed in a 37°C water bath for 15s. Motile fractions were selected by swim-up, then incubated for 90 mm in TALP with 10 ?g heparin/ml. Each oocyte was positioned with its first polar body at 6 or 12 o'clock by a holding pipette. Sperm (1 ?l) were added to 10 ?l medium containing 10% polyvinylpyrrolidone. A sperm cell was aspirated into a pipette, and then injected head-first into the cytoplasm of an oocyte maintained in H-TCM 199 + 20% FBS at 37°C. Injected oocytes were transferred to HM and, after 90 min, cultured in 50 ?l of BSA-free synthetic oviduct fluid plus polyvinyl alcohol, citrate and non-essential amino acids. Results demonstrate that caprine blastocysts can be produced outside the breeding season by the use of frozen-thawed semen and injection of sperm cells with broken tails into ova followed by culture in defined medium.
650 $aBlastocystis
650 $aGoats
650 $ahyaluronoglucosaminidase
650 $aIonophores
650 $aPharmacology
650 $aCaprino
650 $aEmbrião animal
653 $aAnimal embryos
653 $aCleavage Stage
653 $aFSH
653 $aLH
700 1 $aMORTON, P. C.
700 1 $aSMITH, S. E.
700 1 $aTUCKER, M. J.
700 1 $aSIMPLICIO, A. A.
700 1 $aBRACKETT, B. G.
773 $tZygote$gv. 5, n. 3, p. 261-265, Aug. 1997.
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