韩宇牛附睾尾部冻融精子深度子宫人工授精后受孕率的提高

Sung-Sik Kang, U. Kim, J. Ahn, J. Won, Sang-Rae Cho
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引用次数: 1

摘要

本文研究了深子宫人工授精(DUAI)是否能提高韩宇牛附睾精子人工授精(AI)的受孕率。同步88头韩宇奶牛的发情周期,17头奶牛采用DUAI法结合ES进行人工授精,20头奶牛采用子宫体(BUAI)法结合ES进行人工授精,51头奶牛采用BUAI法进行人工授精作为对照,使用1头成熟公牛冷冻解冻后的射精精子。DUAI法的妊娠率(58.8%)高于BUAI法(25.0%,p = 0.0498)。分别在解冻后和孵育3、6小时后检测ES的运动性。解冻后即刻、孵育后3、6 h,对照组精子快速进行活力显著高于ES组(p < 0.05)。孵育6 h后ES组的直线速度和平均路径速度显著低于对照组(p < 0.05)。ES侧头的线性度和振幅均低于6 h时(p < 0.05)。解冻后即刻和3 h时,鞭毛搏动交叉频率和ES的高激活率均低于对照精子(p < 0.05)。这些运动参数表明,与对照精子相比,ES精子的运动能力和受精能力较低。冻融和孵育3 h后,ES中带完整顶体的活精子比例显著低于射精精子(p < 0.05)。我们的研究结果表明,尽管ES的运动能力、生存能力和受精能力较低,但DUAI方法可以克服ES的低妊娠率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improvement of pregnancy rate after deep uterine artificial insemination with frozen-thawed cauda epididymal spermatozoa in Hanwoo cattle
In the present study, we examined if deep uterine artificial insemination (DUAI) can improve the pregnancy rate of artificial insemination (AI) using epididymal spermatozoa (ES) in Hanwoo cattle. The estrus cycles of 88 Hanwoo cows were synchronized, and 17 cows were artificially inseminated using the DUAI method with ES, 20 cows were artificially inseminated via the uterine body (BUAI) method with ES, and as a control, 51 cows were inseminated by using the BUAI method with ejaculated spermatozoa from 1 proven bull after frozen thawing. The pregnancy rate of the DUAI method (58.8%) was higher than that of the BUAI method (25.0%, p = 0.0498). The motility of ES was examined immediately after thawing and after 3 and 6 h of incubation. The rapid progressive sperm motility of the control group was significantly higher than that of the ES group immediately after thawing and after 3 and 6 h of incubation (p < 0.05). The straight line velocity and average path velocity of the ES group after 6 h of incubation were significantly lower than those in the control group (p < 0.05). The linearity and amplitude of lateral head of ES were lower than those at 6 h (p < 0.05). The flagellar beat cross frequency and hyperactivation of ES were lower than the control spermatozoa immediately after thawing and at 3 h (p < 0.05). These motility parameters suggested that ES had a low motility and fertilization ability compared to the control spermatozoa. After frozen-thawing and 3 h of incubation, the percentage of live spermatozoa with intact acrosomes in the ES was significantly lower than that in ejaculated spermatozoa (p < 0.05). Our findings suggested that the DUAI method can overcome the low pregnancy rate of ES, despite the low motility, viability, and fertilization ability of ES.
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