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Fertility of frozen-thawed stallion semen cannot be predicted by the currently used laboratory methods

机译:当前使用的实验室方法无法预测冷冻解冻的公马精液的生育能力

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摘要

The aim of the project was to use current simple and practical laboratory tests and compare results with the foaling rates of mares inseminated with commercially produced frozen semen. In Exp. 1, semen was tested from 27 and in Exp. 2 from 23 stallions; 19 stallions participated in both experiments. The mean number of mares per stallion in both experiments was 37 (min. 7, max. 121). Sperm morphology was assessed and bacterial culture performed once per stallion. In Exp. 1, progressive motility after 0, 1, 2, 3, and 4 h of incubation using light microscopy, motility characteristics measured with an automatic sperm analyzer, plasma membrane integrity using carboxyfluorescein diacetate/propidium iodide (CFDA/PI) staining and light microscopy, plasma membrane integrity using PI staining and a fluorometer, plasma membrane integrity using a resazurin reduction test, and sperm concentration were evaluated. In Exp. 2, the same tests as in Exp. 1 and a hypo-osmotic swelling test (HOST) using both light microscopy and a fluorometer were performed immediately after thawing and after a 3-h incubation. Statistical analysis was done separately to all stallions and to those having ≥ 20 mares; in addition, stallions with foaling rates < 60 or ≥ 60% were compared. In Exp. 1, progressive motility for all stallions after a 2 – 4-h incubation correlated with the foaling rate (correlation coefficients 0.39 – 0.51), (p < 0.05). In stallions with > 20 mares, the artificial insemination dose showed a correlation coefficient of -0.58 (p < 0.05). In Exp. 2, the HOST immediately after thawing showed a negative correlation with foaling rate (p < 0.05). No single test was consistently reliable for predicting the fertilizing capacity of semen, since the 2 experiments yielded conflicting results, although the same stallions sometimes participated in both. This shows the difficulty of frozen semen quality control in commercially produced stallion semen, and on the other hand, the difficulty of conducting fertility trials in horses.
机译:该项目的目的是使用当前简单而实用的实验室测试,并将结果与​​用商业化生产的冷冻精液授精的母马的产驹率进行比较。在实验中1,精液从27开始进行实验。 23种种马中的2种; 19个种马参加了两个实验。在两个实验中,每匹公马的平均母马数为37(最小7,最大121)。评估精子形态,每个种马进行一次细菌培养。在实验中1,使用光学显微镜孵育0、1、2、3和4小时后的进行性运动,使用自动精子分析仪测量的运动特性,使用二乙酸羧基荧光素/碘化丙啶(CFDA / PI)染色和光学显微镜的质膜完整性,使用PI染色和荧光计测量血浆膜完整性,使用刃天青还原试验检测血浆膜完整性,并评估精子浓度。在实验中2,与Exp。中相同的测试。融化后和孵育3小时后立即进行光学显微镜检查和荧光计进行图1和低渗透溶胀试验(HOST)。对所有公马和≥20匹母马进行统计分析;此外,还比较了驹率<60或≥60%的种马。在实验中如图1所示,孵育2 – 4-h后所有种马的渐进运动能力与马驹生成率相关(相关系数0.39 – 0.51),(p <0.05)。在母马数大于20的种马中,人工授精剂量的相关系数为-0.58(p <0.05)。在实验中如图2所示,融化后的HOST与产驹率呈负相关(p <0.05)。尽管这两次实验有时会产生相同的结果,但没有两次测试能够一致可靠地预测精液的受精能力。这表明在商业生产的种马精液中冷冻精液质量控制很困难,另一方面,在马中进行生育力试验也很困难。

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