作者: E. Mocé , E. Blanch , A. Talaván , M. P. Viudes de Castro
DOI: 10.1071/RD14009
关键词: Anatomy 、 Animal science 、 Litter (animal) 、 Reproductive biology 、 Reproductive technology 、 Human fertilization 、 Biology 、 Spermatogenesis 、 Cryopreservation 、 Liquid nitrogen 、 Embryo culture
摘要: The freezing step of the cryopreservation protocol negatively influences quality and fertilising ability rabbit spermatozoa. This study determines effect different rates on spermatozoa cryopreserved with dimethylsulfoxide (DMSO) (1.75M) sucrose (0.05M). Ejaculates from meat line males (n=12) were pooled each pool (n=7) was split into four aliquots. One group straws (control, C) frozen in static liquid nitrogen vapour (5cm above nitrogen, 10min) other groups at (°Cmin(-1)) -6°C to -100°C using a programmable freezer: slow (-15°Cmin(-1), S), medium (-40°Cmin(-1), M) or fast (-60°Cmin(-1), F). After thawing (50°C, 12s), highest (P<0.05) C M samples lowest S F samples. presented litter sizes (P≤0.05) fertility whilst exhibited values. In conclusion, rate affects both frozen-thawed spermatozoa, (-15°Cmin(-1)) (-60°Cmin(-1)) being detrimental for ability.