In vitro developmental competence of alpaca (Vicugna pacos) and llama (Lama glama) oocytes after parthenogenetic activation

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datacite.alternateIdentifier.citationSMALL RUMINANT RESEARCH,Vol.133,148-152,2015
datacite.alternateIdentifier.doi10.1016/j.smallrumres.2015.08.014
datacite.creatorRuiz, Jaime
datacite.creatorLandeo, Leandra
datacite.creatorMendoza, Jose
datacite.creatorCorrea, Jorge
datacite.creatorSilva Jiménez, Mauricio
datacite.creatorRatto, Marcelo H.
datacite.date2015
datacite.subject.englishAlpaca
datacite.subject.englishLlama
datacite.subject.englishOocytes
datacite.subject.englishChemical activation
datacite.subject.englishBlastocyst
datacite.titleIn vitro developmental competence of alpaca (Vicugna pacos) and llama (Lama glama) oocytes after parthenogenetic activation
dc.date.accessioned2021-04-30T16:58:26Z
dc.date.available2021-04-30T16:58:26Z
dc.description.abstractThe study was designed to compare the cleavage and blastocysts rate of in vitro matured alpaca and llama oocytes after chemical activation. Alpaca (n=90) and llama (n=85) ovaries were collected at a local slaughterhouse and transported within 2-3 h to the laboratory. Cumulus oocyte complexes (COCs) were aspirated from follicles 2-6 mm in diameter and classified according to the number of cumulus cell layers and cytoplasm morphology. A total of 350 and 4000005 were collected from the alpaca and llama abattoir-derived ovaries, respectively (average, 3.8 vs. 4.7COCs per ovary, respectively). Only category 1 and 2COCs collected from alpaca (n=280) and llama (n=340) were in vitro matured for 26-28 h in medium TCM 199 at 39 degrees C in an atmosphere of 5% CO2 in humidified air. After in vitro maturation, oocytes were denuded of cumulus cells by vortex agitation, for 2 min in mSOF-HEPES solution at 0.1% hyaluronidase. Mature (MB) alpaca (n=224) and llama (n=240) oocytes were activated using 5 mu M lonomycin in SOF-HEPES supplemented with 1 mg/ml BSA at room temperature for 4 min followed by incubation in mSOF-IVC supplemented with 3 mg/ml BSA, 2 mM 6-dimethylaminopurine (6-DMAP) and 12.5 mu M cytochalasin B for 3 h at 39 degrees C in an atmosphere of 5% O-2,5% CO2 and 90% N-2 in humidified air. Then, oocytes were transferred to 40 mu l drops of mSOF-IVC supplemented with 3 mg/ml BSA and cultured for 8 days at 39 degrees C in an atmosphere of 5% O-2, 5% CO2 and 90% N-2 in humidified air. A greater proportion of category 3COCs was collected from alpaca than llama ovaries; however, there were not significant differences in the remaining COCs categories between species. A total of 224 and 240 alpaca and llama matured oocytes were chemically activated, respectively. Cleavage (62.5 +/- 2.7 vs. 66.6 +/- 5.2), morula (47.0 +/- 2.0 vs. 45.8 +/- 1.4) and blastocyst (22.5 +/- 13 vs. 18.7 +/- 1.0) development rate did not differ between groups. In conclusion, alpaca and llama oocytes can be effectively activated after a sequential incubation with 5 mu M lonomycin and 2 mM 6-DMAP/12.5 mu M cytochalasin B resulting in consistent in vitro embryo development rates that could be used to assess oocyte viability/functionality after in vitro maturation or cryopreservation. (C) 2015 Elsevier B.V. All rights reserved.
dc.identifier.urihttp://repositoriodigital.uct.cl/handle/10925/3686
dc.language.isoen
dc.publisherELSEVIER SCIENCE BV
dc.sourceSMALL RUMINANT RESEARCH
oaire.resourceTypeArticle
uct.catalogadorWOS
uct.indizacionSCI
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