Gañán N, González R, Sestelo A, Garde J J, Sánchez I, Aguilar J M, Gomendio M, Roldan E R S
Reproductive Ecology and Biology Group, Museo Nacional de Ciencias Naturales (CSIC), 28006 Madrid, Spain.
Theriogenology. 2009 Aug;72(3):341-52. doi: 10.1016/j.theriogenology.2009.03.002. Epub 2009 May 1.
There is limited information on bobcat ejaculate traits and sperm cryopreservation and fertilizing ability. Bobcats were electroejaculated under general anesthesia in November (autumn) and April (spring), and endocrine and sperm traits were characterized. Testosterone (mean+/-SEM: 0.90+/-0.15 ng/mL) was not different between sampling times, but cortisol (average: 13.95+/-1.73 microg/dL) was significantly higher in April. Average number of spermatozoa was 10.0+/-3.4 x 10(6) sperm/ejaculate, with values being significantly higher in April. Sperm motility (average 55.7+/-5.8% motile sperm) was not different between sampling times. The proportion of normal spermatozoa in the ejaculate (average: 14.7+/-2.1%) was significantly higher in April, but the percentage of spermatozoa with intact acrosomes (average: 43.7+/-3.8%) was significantly higher in autumn. Spermatozoa were cryopreserved in a Tes-Tris-based diluent (TEST) or Biladyl, both containing 20% egg yolk and 4% glycerol. Diluted sperm were loaded into straws, refrigerated using a programmable thermoblock with a dry chamber, frozen in nitrogen vapors, thawed, and incubated in F-10 medium with 5% fetal bovine serum for up to 3h. After cryopreservation in TEST, there were about 50% motile sperm upon thawing, and survival was high during incubation post-thaw. Cryopreservation in Biladyl led to similar results, but motility decreased substantially during incubation post-thaw. Bobcat spermatozoa fertilized domestic cat oocytes matured in vitro. Fertilization rates were higher for sperm collected in April and cryopreserved in TEST (46%) than for those cryopreserved using Biladyl (<3%). Fertilized oocytes cleaved in culture, and some (27%) reached the morula stage. This study has allowed us to gain further baseline information on bobcat reproduction, explore sperm cryopreservation conditions, and show that fertilizing capacity can be tested using in vitro-matured cat oocytes. These results will be important for future conservation efforts.
关于短尾猫射精特征、精子冷冻保存及受精能力的信息有限。在11月(秋季)和4月(春季)对短尾猫进行全身麻醉后进行电刺激采精,并对内分泌和精子特征进行了表征。两次采样时睾酮水平(均值±标准误:0.90±0.15 ng/mL)无差异,但4月的皮质醇水平(均值:13.95±1.73 μg/dL)显著更高。平均精子数量为10.0±3.4×10⁶个精子/次射精,4月的数值显著更高。两次采样时精子活力(平均55.7±5.8%有活力精子)无差异。射精中正常精子的比例(平均:14.7±2.1%)在4月显著更高,但顶体完整的精子百分比(平均:43.7±3.8%)在秋季显著更高。精子保存在基于Tes-Tris的稀释液(TEST)或Biladyl中,两者均含有20%蛋黄和4%甘油。将稀释后的精子装入细管,使用带干燥腔的可编程热块冷藏,在液氮蒸汽中冷冻,解冻后在含5%胎牛血清的F-10培养基中孵育长达3小时。在TEST中冷冻保存后,解冻时有约50%的有活力精子,解冻后孵育期间存活率较高。在Biladyl中冷冻保存导致类似结果,但解冻后孵育期间活力大幅下降。短尾猫精子使体外成熟的家猫卵母细胞受精。4月采集并在TEST中冷冻保存的精子受精率(46%)高于使用Biladyl冷冻保存的精子(<3%)。受精的卵母细胞在培养中分裂,一些(27%)达到桑椹胚阶段。这项研究使我们能够获得关于短尾猫繁殖的更多基线信息,探索精子冷冻保存条件,并表明可以使用体外成熟的猫卵母细胞测试受精能力。这些结果对未来的保护工作将很重要。