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Quality control of refrigerated and cryopreserved semen using computer-assisted sperm analysis (CASA), viable staining and standardized fertilization in African catfish (Clarias gariepinus)

机译:使用计算机辅助精子分析(CASA),可行的染色和标准化施肥对非洲cat鱼(Clarias gariepinus)进行冷冻和冷冻精液质量控制

摘要

A new integrated approach including computer-assisted sperm analysis (CASA), viability staining and fertilization was used to study the quality of cryodiluents used in fish sperm cryopreservation. As an example the sperm quality of an African catfish, Clarias gariepinus (Burchell, 1822), was assessed by its fertilizing ability, motility and viability at day 0 (fresh), after 2 days' storage at 4 degreesC and after 2 days, 5 months and 10 months frozen at -196 degreesC using solutions containing dimethyl sulphoxide (DMSO) or glycerol as permeating cryoprotectants. Four of the best freezing solutions were used, namely, Steyn's extender (S1, S4) and Mounib's extender (M3, M4) associating 10% hen's egg yolk. Progressive sperm movement measured by CASA and expressed by the straight line velocity (VSL), the average path velocity (VAP) and the curvilinear velocity (VCL) was highly correlated with hatching rates obtained from fertilization using minimal sperm:egg ratios. After 2 days, the motility of spermatozoa frozen with DMSO and 10% egg yolk had deteriorated less than that of spermatozoa stored at 4 degreesC. Post-thaw hatching rates reflected the post-thaw sperm viability, which was cryodiluent dependent: 14.9+/-2.0% (S4), 17.0+/-4.2% (S1), 25.9+/-3.7% (M4) and 52.1+/-3.4% (M3) after 5 months of cryopreservation. The percent motility of 10-months-frozen spermatozoa was high in M3 (70.7+/-11.4%) and M4 (64.0+/-2.0%) cryoprotected sperm when measured between 5 and 20 sec after activation, but decreased rapidly to 24.3+/-8.3% (M3) and 23.0+/-9.0% (M4) between 21 and 35 sec after activation. Mounib's extender (M3, M4) provided the best cryoprotection to the spermatozoa for all post-thaw sperm quality measurements and at all freezing durations. Sperm motility was positively related to fertility. Our method will make it possible to develop even better extenders and cryoprotectants.
机译:一种新的综合方法,包括计算机辅助精子分析(CASA),活力染色和受精,用于研究鱼精子冷冻保存中使用的冷冻稀释剂的质量。例如,非洲cat鱼(Clarias gariepinus,Burchell,1822年)的精子质量通过在0℃(新鲜),在4℃下保存2天和在2天之后5的受精能力,运动性和活力进行评估。使用含有二甲基亚砜(DMSO)或甘油作为防冻剂的溶液在-196摄氏度下冷冻15个月和10个月。使用了四种最佳的冷冻溶液,分别是Steyn的增量剂(S1,S4)和Mounib的增量剂(M3,M4),可将10%的母鸡卵黄结合在一起。通过CASA测量并以直线速度(VSL),平均路径速度(VAP)和曲线速度(VCL)表示的渐进式精子运动与以最小精子:卵子比率从受精获得的孵化率高度相关。 2天后,用DMSO和10%蛋黄冷冻的精子的运动性恶化小于在4℃下储存的精子的运动性。解冻后的孵化率反映了解冻后精子的活力,这取决于冷冻稀释剂:14.9 +/- 2.0%(S4),17.0 +/- 4.2%(S1),25.9 +/- 3.7%(M4)和52.1+冷冻保存5个月后,-/ 3.4%(M3)。冷冻后10个月冷冻的精子的活力百分比在激活后5到20秒内测量时在M3(70.7 +/- 11.4%)和M4(64.0 +/- 2.0%)冷冻保护的精子中较高,但迅速下降至24.3+激活后21到35秒之间,误差为--8.3%(M3)和23.0 +/- 9.0%(M4)。 Mounib的补充剂(M3,M4)可在所有解冻后的精子质量测量和所有冷冻期间为精子提供最佳的冷冻保护。精子活力与生育能力呈正相关。我们的方法将有可能开发出更好的增量剂和防冻剂。

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