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Morphofunctional Characterization of Cooled Sperm With Different Extenders to Use in Equine-Assisted Reproduction

Florez-Rodriguez, Shirley Andrea, de Arruda, Rubens Paes, Alves, Maíra Bianchi Rodrigues, Affonso, Fernanda Jordão, Carvalho, Henrique Fulaneti, Lemes, Kleber Menegon, Lançoni, Renata, de Andrade, André Furugen Cesar, Celeghini, Eneiva Carla Carvalho
Journal of equine veterinary science 2014 v.34 no.7 pp. 911-917
Pisum sativum, acrosome, agglutinins, analysis of variance, assisted reproductive technologies, bovine serum albumin, chromatin, cooling, fluorescein, iodides, membrane potential, microscopy, mitochondrial membrane, plasma membrane, propidium, semen, semen extenders, sex determination analysis, skim milk, sperm motility, stallions, toluidine blue
The aim of this study was to assess extenders for cooling equine semen at 5°C and to be used in assisted reproductive technologies (ARTs). Four ejaculates were obtained from each of four stallions. Gel-free semen was diluted in three different extenders: (1) SMK, an opaque skim milk–based extender; (2) SMT, a skim milk (65%) and Tyrode medium (35%); and (3) BSAG, a clear extender containing 1% bovine serum albumin. Samples were packaged (10 mL; 50 × 106 sperm/mL) and stored in a cooling device at 5°C for 12 hours. Analyses were done at 0, 4, 8, and 12 hours after cooling. Semen was analyzed for sperm motility characteristics using a computer-assisted sperm analysis, for plasma membrane and acrosome integrity and mitochondrial membrane potential, using fluorescent probes (propidium iodide, Hoechst 33342, fluorescein isothiocyanate–conjugated Pisum sativum agglutinin, and 5,5′,6,6′-tetrachloro-1,1′,3,3′-tetraethylbenzimidazolyl carbocyanine iodide [JC-1]). Morphology was evaluated with differential interference contrast microscopy and sperm chromatin integrity by the toluidine blue technique. Data were analyzed by analysis of variance and by Tukey test, with time as a repeated measure (SAS, 1998), when P < .05 was significant. In general, milk-based extenders (SMT and SMK) showed improved maintenance of semen quality compared with BSAG. Finally, the addition of skim milk to equine semen extender for cooling at 5°C for 12 hours seems to play a crucial role in sperm preservation. Although, optically clearer extenders are desired for use in ARTs, such as sperm sexing, the milk-free extender (BSAG) is less efficient for cooled-stored equine semen.