Lipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrification

Detalhes bibliográficos
Autor(a) principal: Sudano, Mateus Jose [UNESP]
Data de Publicação: 2011
Outros Autores: 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]
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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spelling 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
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dc.identifier.doi.none.fl_str_mv 10.1016/j.theriogenology.2010.11.033