Sperm cryopreservation with supplementation of a-tocopherol and ascorbic acid in freezing media increase sperm function and fertility rate in Atlantic salmon (Salmo salar)

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datacite.alternateIdentifier.citationAquaculture, Vol.493, 1-8en_US
datacite.alternateIdentifier.doi10.1016/j.aquaculture.2018.04.046en_US
datacite.creatorFigueroa Villalobos, Elías
datacite.creatorFarias, J.G.
datacite.creatorLee Estevez, M.
datacite.creatorValdebenito Isler, Iván
datacite.creatorRisopatron, J.
datacite.creatorMagnotti, C.
datacite.creatorRomero, J.
datacite.creatorWatanabe, I.
datacite.creatorOliveira, R.P.S.
datacite.date2018
datacite.subjectDefensas antioxidantesen_US
datacite.subjectÁcido ascórbicoen_US
datacite.subjectCriopreservaciónen_US
datacite.subjectSalmo Salaren_US
datacite.titleSperm cryopreservation with supplementation of a-tocopherol and ascorbic acid in freezing media increase sperm function and fertility rate in Atlantic salmon (Salmo salar)en_US
dc.date.accessioned2020-07-07T15:25:20Z
dc.date.available2020-07-07T15:25:20Z
dc.description.abstractThe use of α-tocopherol and ascorbic acid in freezing medium prevents lipoperoxidation and damage by ROS (reactive oxygen species); however, the effects of these antioxidants in salmonid spermatozoa have not been studied. In this work the protective effects of antioxidants on the enzymatic activity and fertilization capacity of frozen Atlantic salmon spermatozoa were studied. Spermatozoa were frozen in Cortland® medium supplemented with 1.3 M DMSO, 0.3 M glucose, 2% BSA and different concentrations of α-tocopherol and ascorbic acid; spermatozoa frozen without antioxidants were used as control and fresh sperm. Samples loaded in 0.5 ml plastic straws were frozen at 68 °C/min (Freeze Control®). Thawing was carried out at 35 °C and post-thawing lipid peroxidation (LPO) was evaluated along with Glutathione (GSH/GSSG) levels; and Glutathione peroxidase (GPx) and Catalase (CAT) activity. Additionally, percentage of motility, mitochondrial membrane potential (ΔΨM), and fertilization rate were assessed. Results showed significantly lower LPO values (expressed as malondialdehyde concentration) in spermatozoa cryopreserved with α-tocopherol (0.1 mM and 0.5 mM) and with combinations of α-tocopherol/ascorbic acid (0.1 mM/1.0 mM and 0.5 mM/10 mM ratios) (p <.05). Moreover, spermatozoa frozen with α-tocopherol/ascorbic acid also exhibited significantly higher GPx and CAT activity as well as GSH/GSSG ratio compared to controls (p <.05). The production of O2 − i also decreased with the combined treatment, however, no statistically significant difference was found compared to controls. Consistently with the improvement in antioxidant defences, the percentage of motility and ΔΨM were highest and significantly different in spermatozoa cryopreserved with α-tocopherol/ascorbic acid 0.1 mM/1.0 mM compared to controls, supporting the significantly higher fertilization rate exhibited by spermatozoa under the same treatmenten_US
dc.formatPDFen_US
dc.identifier.urihttp://repositoriodigital.uct.cl/handle/10925/2260
dc.language.isoenen_US
dc.rightsObra bajo licencia Creative Commons 3.0en_US
oaire.resourceTypeArtículo de Revistaen_US
uct.catalogadormlmen_US
uct.comunidadRecursos Naturalesen_US
uct.disciplinaBiología Marinaen_US
uct.indizacionSCOPUSen_US
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