Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1016/j.theriogenology.2010.11.033 |
Texto Completo: | http://dx.doi.org/10.1016/j.theriogenology.2010.11.033 http://hdl.handle.net/11449/14698 |
Resumo: | The objective was to evaluate supplementation of fetal calf serum (FCS) and phenazine ethosulfate (PES), a metabolic regulator that inhibits fatty acid synthesis, in culture media during in vitro production (IVP) of bovine embryos. Taking oocyte fertilization (n = 4,320) as Day 0, four concentrations of FCS (0, 2.5, 5, and 10%) and three periods of exposure to PES (without addition-Control; after 60 h-PES Day 2.5 of embryo culture; and after 96 h-PES Day 4) were evaluated. Increasing FCS concentration in the culture media enhanced lipid accumulation (P < 0.05), increased apoptosis in fresh (2.5%: 19.1 +/- 1.8 vs 10%: 28.4 +/- 2.3, P < 0.05; mean +/- SEM) and vitrified (2.5%: 42.8 +/- 2.7 vs 10%: 69.2 +/- 3.4, P < 0.05) blastocysts, and reduced blastocoele re-expansion after vitrification (2.5%: 81.6 +/- 2.5 vs 10%: 67.3 +/- 3.5, P < 0.05). The addition of PES in culture media, either from Days 2.5 or 4, reduced lipid accumulation (P < 0.05) and increased blastocoele re-expansion after vitrification (Control: 72.0 +/- 3.0 vs PES Day 2.5: 79.9 +/- 2.8 or PES Day 4: 86.2 +/- 2.4, P < 0.05). However, just the use of PES from D4 reduced apoptosis in vitrified blastocysts (Control: 52.0 +/- 3.0 vs PES Day 4: 39.2 +/- 2.4, P < 0.05). Independent of FCS withdrawal or PES addition to culture media, the in vivo control group had lesser lipid accumulation, a lower apoptosis rate, and greater cryotolerance (P < 0.05). The increased lipid content was moderately correlated with apoptosis in vitrified blastocysts (r = 0.64, P = 0.01). In contrast, the increased apoptosis in fresh blastocysts was strongly correlated with apoptosis in vitrified blastocysts (r = 0.94, P < 0.0001). Therefore, using only 2.5% FCS and the addition of PES from Day 4, increased the survival of IVP embryos after vitrification. Moreover, embryo quality, represented by the fresh apoptosis rate, was better than lipid content for predicting embryo survival after vitrification. (C) 2011 Elsevier B.V. All rights reserved. |
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Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrificationPhenazine ethosulfateFetal calf serumCryotoleranceEmbryo cultureEmbryo survivalThe objective was to evaluate supplementation of fetal calf serum (FCS) and phenazine ethosulfate (PES), a metabolic regulator that inhibits fatty acid synthesis, in culture media during in vitro production (IVP) of bovine embryos. Taking oocyte fertilization (n = 4,320) as Day 0, four concentrations of FCS (0, 2.5, 5, and 10%) and three periods of exposure to PES (without addition-Control; after 60 h-PES Day 2.5 of embryo culture; and after 96 h-PES Day 4) were evaluated. Increasing FCS concentration in the culture media enhanced lipid accumulation (P < 0.05), increased apoptosis in fresh (2.5%: 19.1 +/- 1.8 vs 10%: 28.4 +/- 2.3, P < 0.05; mean +/- SEM) and vitrified (2.5%: 42.8 +/- 2.7 vs 10%: 69.2 +/- 3.4, P < 0.05) blastocysts, and reduced blastocoele re-expansion after vitrification (2.5%: 81.6 +/- 2.5 vs 10%: 67.3 +/- 3.5, P < 0.05). The addition of PES in culture media, either from Days 2.5 or 4, reduced lipid accumulation (P < 0.05) and increased blastocoele re-expansion after vitrification (Control: 72.0 +/- 3.0 vs PES Day 2.5: 79.9 +/- 2.8 or PES Day 4: 86.2 +/- 2.4, P < 0.05). However, just the use of PES from D4 reduced apoptosis in vitrified blastocysts (Control: 52.0 +/- 3.0 vs PES Day 4: 39.2 +/- 2.4, P < 0.05). Independent of FCS withdrawal or PES addition to culture media, the in vivo control group had lesser lipid accumulation, a lower apoptosis rate, and greater cryotolerance (P < 0.05). The increased lipid content was moderately correlated with apoptosis in vitrified blastocysts (r = 0.64, P = 0.01). In contrast, the increased apoptosis in fresh blastocysts was strongly correlated with apoptosis in vitrified blastocysts (r = 0.94, P < 0.0001). Therefore, using only 2.5% FCS and the addition of PES from Day 4, increased the survival of IVP embryos after vitrification. Moreover, embryo quality, represented by the fresh apoptosis rate, was better than lipid content for predicting embryo survival after vitrification. (C) 2011 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)UNESP, São Paulo State Univ, Sch Vet Med & Anim Sci, FMVZ,Dept Anim Reprod & Vet Radiol, BR-18618970 Botucatu, SP, BrazilUNESP, São Paulo State Univ, Sch Vet Med & Anim Sci, FMVZ,Dept Anim Reprod & Vet Radiol, BR-18618970 Botucatu, SP, BrazilFAPESP: 07/57766-4FAPESP: 08/51378-5Elsevier B.V.Universidade Estadual Paulista (Unesp)Sudano, Mateus Jose [UNESP]Paschoal, Daniela Martins [UNESP]Rascado, Tatiana da Silva [UNESP]Ona Magalhaes, Luis Carlos [UNESP]Crocomo, Leticia Ferrari [UNESP]de Lima-Neto, Joao Ferreira [UNESP]Landim-Alvarenga, Fernanda da Cruz [UNESP]2013-09-30T18:29:06Z2014-05-20T13:42:17Z2013-09-30T18:29:06Z2014-05-20T13:42:17Z2011-04-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1211-1220application/pdfhttp://dx.doi.org/10.1016/j.theriogenology.2010.11.033Theriogenology. New York: Elsevier B.V., v. 75, n. 7, p. 1211-1220, 2011.0093-691Xhttp://hdl.handle.net/11449/1469810.1016/j.theriogenology.2010.11.033WOS:000289180900005WOS000289180900005.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengTheriogenology2.136info:eu-repo/semantics/openAccess2024-09-09T14:01:08Zoai:repositorio.unesp.br:11449/14698Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-09T14:01:08Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification |
title |
Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification |
spellingShingle |
Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification Sudano, Mateus Jose [UNESP] Phenazine ethosulfate Fetal calf serum Cryotolerance Embryo culture Embryo survival Sudano, Mateus Jose [UNESP] Phenazine ethosulfate Fetal calf serum Cryotolerance Embryo culture Embryo survival |
title_short |
Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification |
title_full |
Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification |
title_fullStr |
Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification |
title_full_unstemmed |
Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification |
title_sort |
Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification |
author |
Sudano, Mateus Jose [UNESP] |
author_facet |
Sudano, Mateus Jose [UNESP] Sudano, Mateus Jose [UNESP] Paschoal, Daniela Martins [UNESP] Rascado, Tatiana da Silva [UNESP] Ona Magalhaes, Luis Carlos [UNESP] Crocomo, Leticia Ferrari [UNESP] de Lima-Neto, Joao Ferreira [UNESP] Landim-Alvarenga, Fernanda da Cruz [UNESP] Paschoal, Daniela Martins [UNESP] Rascado, Tatiana da Silva [UNESP] Ona Magalhaes, Luis Carlos [UNESP] Crocomo, Leticia Ferrari [UNESP] de Lima-Neto, Joao Ferreira [UNESP] Landim-Alvarenga, Fernanda da Cruz [UNESP] |
author_role |
author |
author2 |
Paschoal, Daniela Martins [UNESP] Rascado, Tatiana da Silva [UNESP] Ona Magalhaes, Luis Carlos [UNESP] Crocomo, Leticia Ferrari [UNESP] de Lima-Neto, Joao Ferreira [UNESP] Landim-Alvarenga, Fernanda da Cruz [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Sudano, Mateus Jose [UNESP] Paschoal, Daniela Martins [UNESP] Rascado, Tatiana da Silva [UNESP] Ona Magalhaes, Luis Carlos [UNESP] Crocomo, Leticia Ferrari [UNESP] de Lima-Neto, Joao Ferreira [UNESP] Landim-Alvarenga, Fernanda da Cruz [UNESP] |
dc.subject.por.fl_str_mv |
Phenazine ethosulfate Fetal calf serum Cryotolerance Embryo culture Embryo survival |
topic |
Phenazine ethosulfate Fetal calf serum Cryotolerance Embryo culture Embryo survival |
description |
The objective was to evaluate supplementation of fetal calf serum (FCS) and phenazine ethosulfate (PES), a metabolic regulator that inhibits fatty acid synthesis, in culture media during in vitro production (IVP) of bovine embryos. Taking oocyte fertilization (n = 4,320) as Day 0, four concentrations of FCS (0, 2.5, 5, and 10%) and three periods of exposure to PES (without addition-Control; after 60 h-PES Day 2.5 of embryo culture; and after 96 h-PES Day 4) were evaluated. Increasing FCS concentration in the culture media enhanced lipid accumulation (P < 0.05), increased apoptosis in fresh (2.5%: 19.1 +/- 1.8 vs 10%: 28.4 +/- 2.3, P < 0.05; mean +/- SEM) and vitrified (2.5%: 42.8 +/- 2.7 vs 10%: 69.2 +/- 3.4, P < 0.05) blastocysts, and reduced blastocoele re-expansion after vitrification (2.5%: 81.6 +/- 2.5 vs 10%: 67.3 +/- 3.5, P < 0.05). The addition of PES in culture media, either from Days 2.5 or 4, reduced lipid accumulation (P < 0.05) and increased blastocoele re-expansion after vitrification (Control: 72.0 +/- 3.0 vs PES Day 2.5: 79.9 +/- 2.8 or PES Day 4: 86.2 +/- 2.4, P < 0.05). However, just the use of PES from D4 reduced apoptosis in vitrified blastocysts (Control: 52.0 +/- 3.0 vs PES Day 4: 39.2 +/- 2.4, P < 0.05). Independent of FCS withdrawal or PES addition to culture media, the in vivo control group had lesser lipid accumulation, a lower apoptosis rate, and greater cryotolerance (P < 0.05). The increased lipid content was moderately correlated with apoptosis in vitrified blastocysts (r = 0.64, P = 0.01). In contrast, the increased apoptosis in fresh blastocysts was strongly correlated with apoptosis in vitrified blastocysts (r = 0.94, P < 0.0001). Therefore, using only 2.5% FCS and the addition of PES from Day 4, increased the survival of IVP embryos after vitrification. Moreover, embryo quality, represented by the fresh apoptosis rate, was better than lipid content for predicting embryo survival after vitrification. (C) 2011 Elsevier B.V. All rights reserved. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-04-15 2013-09-30T18:29:06Z 2013-09-30T18:29:06Z 2014-05-20T13:42:17Z 2014-05-20T13:42:17Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.theriogenology.2010.11.033 Theriogenology. New York: Elsevier B.V., v. 75, n. 7, p. 1211-1220, 2011. 0093-691X http://hdl.handle.net/11449/14698 10.1016/j.theriogenology.2010.11.033 WOS:000289180900005 WOS000289180900005.pdf |
url |
http://dx.doi.org/10.1016/j.theriogenology.2010.11.033 http://hdl.handle.net/11449/14698 |
identifier_str_mv |
Theriogenology. New York: Elsevier B.V., v. 75, n. 7, p. 1211-1220, 2011. 0093-691X 10.1016/j.theriogenology.2010.11.033 WOS:000289180900005 WOS000289180900005.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Theriogenology 2.136 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1211-1220 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1822183849432449024 |
dc.identifier.doi.none.fl_str_mv |
10.1016/j.theriogenology.2010.11.033 |