温热增精剂对猪采集后精子质量的影响

K. W. Lovercamp, A. Giri
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摘要

在养猪业中用于人工授精(AI)的精液通常被收集到一个装有空收集袋的温暖的精液收集杯中。如果环境温度与收集时加热的收集杯和精液的温度不密切匹配,那么由于温度冲击,可能会对精子细胞的活力和形态产生负面影响。本研究的目的是确定将猪精液直接收集到加热至38.5°C的精液扩展器中是否会影响收集后的精子质量。7头性成熟的伯克夏×杜洛克杂交公猪每周采集一次精液,连续采集4周。每隔一次采集,将公猪的精液收集到加热到38.5°C的收集杯和塑料收集袋中,其中要么不含精液扩展剂(对照组),要么含有100毫升加热到38.5°C的市售长期精液扩展剂(治疗组)。收集和处理后,将精液延长至37.5 × 106个/mL,在精液冷却器中保存6天,温度为17°C。分别于第0天(采集日)和第6天进行运动和形态学评价。无x天治疗效果(P > 0.05)。治疗组与对照组精子活力(82.2 vs. 75.2%)和精子进行性活力(64.1 vs. 53.5%)差异有统计学意义(P = 0.03)。与对照组相比,治疗组正常精子形态无差异(P = 0.96)(89.1比89.0%)。这些数据表明,与加热到38.5°C不含精液扩展剂的收集杯和塑料收集袋中收集的猪精液相比,将含有100毫升精液扩展剂的收集杯和塑料收集袋中收集的猪精液具有更高的运动和逐渐运动的精子百分比。
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Effect of warmed semen extender on boar sperm quality post-collection
Semen used for artificial insemination (AI) in the swine industry is typically collected into a warmed semen collection cup containing an empty collection bag. If the ambient temperature does not closely match the temperature of the warmed collection cup and semen at the time of collection then negative effects to the motility and morphology of the sperm cells may occur due to temperature shock. The purpose of this research was to determine if collecting boar semen directly into semen extender warmed to 38.5°C would affect sperm quality post-collection. Sexually mature Berkshire x Duroc crossbred boars (n = 7) were semen collected once per week for four consecutive weeks. Every other collection, the boar's ejaculate was collected into a collection cup and plastic collection bag warmed to 38.5°C containing either no semen extender (control) or 100 mLs of a commercially available long-term semen extender warmed to 38.5°C (treatment). Following collection and processing, the semen was extended to 37.5 × 106 sperm/mL and stored for 6 days post-collection in a semen cooler at 17°C. Motility and morphology were evaluated on day 0 (day of collection) and day 6. There was no day x treatment effect (P > 0.05). Statistical differences (P = 0.03) were found between the treatment and control for sperm motility (82.2 vs. 75.2%) and sperm progressive motility (64.1 vs. 53.5%). No differences (P = 0.96) were present for normal sperm morphology in the treatment compared to the control (89.1 vs. 89.0%). These data suggest that boar semen ejaculates collected into a collection cup and plastic collection bag containing 100 mLs of semen extender warmed to 38.5°C will have greater percentages of motile and progressively motile sperm compared to boar sperm collected into a collection cup and plastic collection bag warmed to 38.5°C containing no semen extender.
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