PENGARUH WAKTU EKUILIBRASI TERHADAP KUALITAS SEMEN BEKU BABI LANDRACE DALAM PENGENCER DURASPERM TERMODIFIKASI (Effect of equilibration time on the quality of landrace boar frozen semen in modified durasperm extender)

Sofia Marlize, T. M. Hine, W. Nalley
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Abstract

This study aims to determine the effect of equilibration time on the quality of landrace spermatozoa both pre- and post-freezing and to find the best equilibration time. The materials used is fresh semen collected from a 2,5 years old landrace boar. Collecting was carried out twice per week using the glove hand method. Semen of good quality (sperm motility ≥70%, sperm concentration ≥200 x 106 cells/ml, and percentage of sperm abnormalities ≤15%) was diluted with durasperm that had been modified with lontar fruit juice, while the cryoprotectants used glycerol and sucrose. Holding time was carried out for 2 hour at 27-28°C, centrifuged at 2000 rpm for 15 minutes, and the sperm sediment was diluted with the same diluent. After that, the liquid semen was packed in a 0.5 mL straw and equilibrated at 3-5°C for 1 (P1), 2 (P2), or 3 hours (P3). The freezing of semen was carried out on the surface of liquid nitrogen at a distance of 5 cm for 10 minutes, and then stored in a liquid nitrogen container. Thawing is done by placing the frozen semen straws in warm water (37°C) for 30 seconds. The research data were analyzed with analysis of variance and continued with the Duncan test. The results showed that the equilibration time at 2 hours (P2) gave the best results (P<0,05) with the mean percentage of motility, viability, abnormality, intact plasma membrane and recovery rate respectively were 30,62%, 58,21%, 4,68%, 58,94% and 43,74%. It was concluded that the equilibration time did not affect the quality of pre-freezing spermatozoa, but it did affect the quality of post-freezing spermatozoa with the best equilibration time to maintain the quality of frozen semen of landrace boar was 2 hours.
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PENGARUH WAKTU EKUILIBRASI TERHADAP KUALITAS SEMEN BEKU BABI LANDRACE DALAM PENGENCER DURASPERM TERMODIFIKASI (平衡时间对改良杜拉胚乳扩展剂中陆地公猪冷冻精液质量的影响)
本研究旨在确定平衡时间对地方精子冷冻前后质量的影响,并寻找最佳的平衡时间。所使用的材料是从一只25岁的长白猪身上采集的新鲜精液。采用手套手法每周采集两次。优质精液(精子活力≥70%,精子浓度≥200 × 106个细胞/ml,精子异常百分比≤15%)用龙塔果汁修饰的硬膜稀释,冷冻保护剂使用甘油和蔗糖。在27-28℃下保温2小时,2000 rpm离心15分钟,用相同的稀释液稀释精子沉淀物。之后,将液体精液装入0.5 mL吸管中,在3-5°C下平衡1 (P1)、2 (P2)或3小时(P3)。将精液在液氮表面5 cm处冷冻10分钟,然后保存在液氮容器中。解冻是通过将冷冻的精液吸管放入温水(37°C) 30秒来完成的。对研究数据进行方差分析,并继续进行Duncan检验。结果表明,平衡时间为2 h (P2)时效果最佳(P< 0.05),平均活力、活力、异常率、完整质膜率和恢复率分别为30、62%、58、21%、4、68%、58、94%和43、74%。综上所述,平衡时间对冷冻前精子质量无影响,但对冷冻后精子质量有影响,维持长白猪冷冻精液质量的最佳平衡时间为2小时。
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