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五种精液稀释剂对冷冻解冻马附睾精子质量影响的比较

Comparison of the Effects of Five Semen Extenders on the Quality of Frozen-Thawed Equine Epididymal Sperm.

作者信息

Neuhauser Stefanie, Bollwein Heinrich, Siuda Matthias, Handler Johannes

机构信息

Pferdezentrum Bad Saarow, Equine Reproduction Unit, Freie Universität Berlin, Bad Saarow, Germany.

Clinic of Reproductive Medicine, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.

出版信息

J Equine Vet Sci. 2019 Aug;79:1-8. doi: 10.1016/j.jevs.2019.05.002. Epub 2019 May 16.

Abstract

Cryopreservation of epididymal sperm allows the saving of genetic material in case of unexpected death or emergency castration. The aim of the present study was the comparison of five different combinations of extenders commercially available for equine frozen semen processing for cryopreservation of epididymal sperm. Epididymal sperm were harvested from gonads of 10 healthy stallions after routine castration by retrograde flush technique. Then, samples were split and diluted with (1) INRA96 + INRA Freeze, (2) BotuSemen + BotuCRIO, (3) EquiPlus + Gent Freeze, (4) EquiPlus + EquiPlus Freeze, and (5) Gent + Gent Freeze. Extenders 1 and 2 showed higher values for total and progressive motility after thawing compared with extender 4 (P < .05). Extender 3 was in between 1 and 2 (P > .05), and extender 5 resulted in the lowest values (P < .05). The subpopulation of viable frozen-thawed sperm with high mitochondrial membrane potential and low intracellular calcium content was higher using extender 1 compared with extenders 3, 4, and 5 (P < .05) and higher in extender 2 compared with extenders 4 and 5 immediately after thawing (P < .05). After 1 hour of incubation, this subpopulation yielded the highest values in extender 2 (P < .05). Immediately after thawing, extender 1 yielded higher values for percentage of DFI and mean DFI than extenders 3, 4, and 5 (P < .05). Following 1 hour of incubation after thawing, sperm processed with extender 1 resulted in the highest values for percentage of DFI and mean DFI (P < .05). Using extender 2, mean DFI values were lower than those in extender 1 and higher than the extenders 3, 4, and 5 (P < .05). The study revealed that according to the examined sperm quality parameters, freezing extenders (extender 1, extender 2) using low concentrations of glycerol either combined with or without methylformamide were beneficial for cryopreservation of stallion epididymal sperm. For processing of stallion epididymal sperm, an extender containing milk proteins (extenders 1-4) for initial dilution after sperm harvesting is preferable to an extender including egg yolk (extender 5).

摘要

附睾精子的冷冻保存可在意外死亡或紧急去势情况下保存遗传物质。本研究的目的是比较市售的五种不同组合的稀释液,这些稀释液用于马冷冻精液处理以冷冻保存附睾精子。通过逆行冲洗技术,从10匹健康种马的性腺中采集附睾精子,常规去势后进行。然后,将样本分开并用以下稀释液稀释:(1)INRA96 + INRA Freeze,(2)BotuSemen + BotuCRIO,(3)EquiPlus + Gent Freeze,(4)EquiPlus + EquiPlus Freeze,以及(5)Gent + Gent Freeze。与稀释液4相比,稀释液1和2解冻后的总活力和前向运动率更高(P <.05)。稀释液3介于1和2之间(P >.05),稀释液5的值最低(P <.05)。使用稀释液1时,线粒体膜电位高且细胞内钙含量低的冷冻解冻后活精子亚群比稀释液3、4和5更高(P <.05),解冻后立即使用稀释液2时,该亚群比稀释液4和5更高(P <.05)。孵育1小时后,该亚群在稀释液2中产生的值最高(P <.05)。解冻后立即使用稀释液1时,DFI百分比和平均DFI的值高于稀释液3、4和5(P <.05)。解冻后孵育1小时后,用稀释液1处理的精子的DFI百分比和平均DFI的值最高(P <.05)。使用稀释液2时,平均DFI值低于稀释液1,高于稀释液第三、4和5(P <.05)。该研究表明,根据所检测的精子质量参数,使用低浓度甘油(无论是否与甲酰胺组合)的冷冻稀释液(稀释液1、稀释液2)有利于种马附睾精子的冷冻保存。对于种马附睾精子的处理,在精子采集后用于初始稀释的含有乳蛋白的稀释液(稀释液1 - 4)比含有蛋黄的稀释液(稀释液5)更可取。

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