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含卵磷酯酶和过氧化氢酶的精液稀释液和用不同增强缓冲液进行第二次稀释对冷藏犬精子质量的影响。

Effects of a lecithin and catalase containing semen extender and a second dilution with different enhancing buffers on the quality of cold-stored canine spermatozoa.

机构信息

Centre for Artificial Insemination and Embryo Transfer, University of Veterinary Science, Vienna, Austria.

出版信息

Theriogenology. 2011 Apr 1;75(6):1095-103. doi: 10.1016/j.theriogenology.2010.11.018. Epub 2011 Feb 4.

Abstract

In the present study, a diluent containing 0.8% lecithin (Minitube®, Tiefenbach, G) for the cold storage of canine semen was compared to a Tris-egg yolk extender (TRIS-EY) containing 20% egg yolk. For this purpose, aliquots of 10 mixed ejaculates (main fractions) were either diluted with TRIS-EY or with three lecithin extenders containing 0.8% lecithin with or without catalase and tyrosine. All samples were examined by computer assisted sperm analysis (CASA), chlortetracycline assay (CTC) and flow cytometry, sperm chromatin structure assay (SCSA) and zona pellucida binding assay (ZBA). Samples were then cold stored for 8 d and examinations repeated at days 3 and 8. Measurement in the CASA were repeated daily and prior to measurement, each sample was diluted with each of 4 enhancers with or without acetylcarnitine. The use of an enhancer proved to be essential for all extenders and after 8 d of cooling, progressive motility (P) and viability (V) still averaged > 70% and > 80% with the lecithin extenders containing additives, whereas with TRIS-EY and without additives it was significantly lower (P < 0.05). The percentage of capacitated spermatozoa did not differ between extender groups and there was no significant increase in acrosome reactions (AR) within 3 d. The chromatin status of cells was not changed by cooling within 8 d. The ZBA showed that with additives, significantly more spermatozoa bound to oocytes when a lecithin extender with additives was used (P < 0.05). In conclusion, the 0.8% lecithin extender containing catalase, conserved P and V during 8 d of cold storage better than the TRIS-EY extender, however, only when an enhancer was used; addition of acetylcarnitine to the enhancer did not further improve semen quality. The here introduced lecithin extender / enhancer combination is a useful tool for prolonged storage of cooled semen with excellent longevity and binding ability; addition of tyrosine to the extender did not improve semen quality.

摘要

在本研究中,将含有 0.8%卵磷酯(Minitube®,Tiefenbach,G)的稀释剂与含有 20%卵黄的 Tris-卵黄稀释剂(TRIS-EY)进行比较,用于犬精液的冷藏。为此,将 10 份混合精液(主要部分)的等分试样分别用 TRIS-EY 或三种含有 0.8%卵磷酯的卵磷酯稀释剂稀释,其中含有或不含有过氧化氢酶和酪氨酸。所有样品均通过计算机辅助精子分析(CASA)、金霉素试验(CTC)和流式细胞术、精子染色质结构分析(SCSA)和透明带结合试验(ZBA)进行检查。然后将样品冷藏 8 天,并在第 3 天和第 8 天重复检查。CASA 中的测量每天重复一次,在测量之前,每个样品都用含有或不含有乙酰肉碱的 4 种增强剂中的每一种进行稀释。事实证明,所有稀释剂都必须使用增强剂,经过 8 天的冷却后,含添加剂的卵磷酯稀释剂的精子活力(P)和活力(V)仍平均> 70%和> 80%,而 TRIS-EY 且无添加剂时,其含量显著降低(P < 0.05)。在不同的稀释剂组中,具有授精能力的精子百分比没有差异,并且在 3 天内顶体反应(AR)没有显著增加。在 8 天内,细胞的染色质状态没有因冷却而改变。透明带结合试验显示,当使用含有添加剂的卵磷酯稀释剂时,显著有更多的精子与卵母细胞结合(P < 0.05)。结论是,含有过氧化氢酶的 0.8%卵磷酯稀释剂在 8 天的冷藏过程中保持了精子的活力(P)和活力(V),优于 TRIS-EY 稀释剂,但是只有在使用增强剂的情况下;将乙酰肉碱添加到增强剂中并不能进一步提高精液质量。这里介绍的卵磷酯稀释剂/增强剂组合是一种有用的工具,可用于延长冷藏精液的储存时间,具有出色的寿命和结合能力;向稀释剂中添加酪氨酸不能提高精液质量。

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