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dc.contributor.authorLeao, B. C. S.-
dc.contributor.authorRocha-Frigoni, N. A. S.-
dc.contributor.authorCabral, E. C.-
dc.contributor.authorCoelho, M. B.-
dc.contributor.authorFerreira, C. R.-
dc.contributor.authorEberlin, M. N.-
dc.contributor.authorAccorsi, M. F.-
dc.contributor.authorNogueira, E.-
dc.contributor.authorMingoti, G. Z.-
dc.date.accessioned2015-10-21T13:10:08Z-
dc.date.accessioned2016-10-25T20:59:41Z-
dc.date.available2015-10-21T13:10:08Z-
dc.date.available2016-10-25T20:59:41Z-
dc.date.issued2015-07-01-
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0093691X15001272-
dc.identifier.citationTheriogenology. New York: Elsevier Science Inc, v. 84, n. 1, p. 127-136, 2015.-
dc.identifier.issn0093-691X-
dc.identifier.urihttp://hdl.handle.net/11449/128469-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/128469-
dc.description.abstractThe aim of this study was to evaluate the effect of supplementing serum-containing media with a mixture of cis- and trans-9,11- and -10,12-conjugated isomers of linoleic acid (CIA) during different steps of the in vitro production (IVM, IVC, or IVM IVC) of bovine embryos on their embryonic development, cryotolerance, and lipid profile. To evaluate the impact of the CIA on membrane lipids, such as phosphatidylcholine (PC) and sphingomyelin (SM), the embryos'lipid profiles were obtained using matrix-assisted laser desorption ionization mass spectrometry. The cleavage rates (78.6%-84.8%) and blastocyst development (44.8%-51.2%) remained unaltered. The postthawing reexpansion rates were higher (P < 0.05) when the CIA was added to the IVM medium (82.6%) or to the IVM + IVC medium (83.8%) than the control (69.3%) or IVC medium (63.0%). Changes in the blastocysts'lipid profile occurred when supplementation was restricted to the IVM or IVC medium. However, the most prominent effects of the CIA on the embryonic PC and SM profiles were observed when the supplement was added to IVM + IVC media, which was an increase in the level of highly unsaturated PCs containing 36 or 38 carbons, which are likely to contain CIA residues. These results showed that the molecular mechanism resulting in the improved cryosurvival, observed with CIA supplementation during bovine embryonic in vitro production, was related to the composition of structural lipids of cellular membranes and is dependent on the treatment length. Monitoring the lipid profile of embryonic membranes may improve the CIA supplementation strategy and facilitate the development of new IVC systems to improve the cryopreservation of bovine embryos and those of other domestic species.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent127-136-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectBovine embryoen
dc.subjectConjugated linoleic aciden
dc.subjectIn vitro productionen
dc.subjectMass spectrometryen
dc.subjectLipid profileen
dc.subjectCryosurvivalen
dc.titleImproved embryonic cryosurvival observed after in vitro supplementation with conjugated linoleic acid is related to changes in the membrane lipid profileen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)-
dc.description.affiliationUniversidade Estadual Paulista (UNESP) - School of Veterinary Medicine, Department of Animal Health, Laboratory of Physiology of Reproduction, Araçatuba, São Paulo, Brazil-
dc.description.affiliationUniversity of Campinas (UNICAMP) - ThoMSon Mass Spectrometry Laboratory, Chemistry Institute, Campinas, São Paulo, Brazil-
dc.description.affiliationBrazilian Agricultural Research Corporation, EMBRAPA Pantanal, Corumbá, Mato Grosso do Sul, Brazil-
dc.description.affiliationUnespUniversidade Estadual Paulista (UNESP) - School of Veterinary Medicine, Department of Animal Health, Laboratory of Physiology of Reproduction, Araçatuba, São Paulo, Brazil-
dc.identifier.doihttp://dx.doi.org/10.1016/j.theriogenology.2015.02.023-
dc.identifier.wosWOS:000355572900017-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofTheriogenology-
dc.identifier.orcid0000-0002-3059-4458pt
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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