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

dc.contributor.authorSudano, Mateus Jose [UNESP]
dc.contributor.authorPaschoal, Daniela Martins [UNESP]
dc.contributor.authorRascado, Tatiana da Silva [UNESP]
dc.contributor.authorOna Magalhaes, Luis Carlos [UNESP]
dc.contributor.authorCrocomo, Leticia Ferrari [UNESP]
dc.contributor.authorde Lima-Neto, Joao Ferreira [UNESP]
dc.contributor.authorLandim-Alvarenga, Fernanda da Cruz [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2013-09-30T18:29:06Z
dc.date.accessioned2014-05-20T13:42:17Z
dc.date.available2013-09-30T18:29:06Z
dc.date.available2014-05-20T13:42:17Z
dc.date.issued2011-04-15
dc.description.abstractThe 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.en
dc.description.affiliationUNESP, São Paulo State Univ, Sch Vet Med & Anim Sci, FMVZ,Dept Anim Reprod & Vet Radiol, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, São Paulo State Univ, Sch Vet Med & Anim Sci, FMVZ,Dept Anim Reprod & Vet Radiol, BR-18618970 Botucatu, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 07/57766-4
dc.description.sponsorshipIdFAPESP: 08/51378-5
dc.format.extent1211-1220
dc.identifierhttp://dx.doi.org/10.1016/j.theriogenology.2010.11.033
dc.identifier.citationTheriogenology. New York: Elsevier B.V., v. 75, n. 7, p. 1211-1220, 2011.
dc.identifier.doi10.1016/j.theriogenology.2010.11.033
dc.identifier.fileWOS000289180900005.pdf
dc.identifier.issn0093-691X
dc.identifier.urihttp://hdl.handle.net/11449/14698
dc.identifier.wosWOS:000289180900005
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofTheriogenology
dc.relation.ispartofjcr2.136
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectPhenazine ethosulfateen
dc.subjectFetal calf serumen
dc.subjectCryotoleranceen
dc.subjectEmbryo cultureen
dc.subjectEmbryo survivalen
dc.titleLipid content and apoptosis of in vitro-produced bovine embryos as determinants of susceptibility to vitrificationen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
unesp.author.orcid0000-0002-6174-3153[5]
unesp.campusUniversidade Estadual Paulista (Unesp), Faculdade de Medicina Veterinária e Zootecnia, Botucatupt
unesp.departmentReprodução Animal e Radiologia Veterinária - FMVZpt

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