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在Tris稀释液中添加α-亚麻酸可提高冻融公牛精液质量。

Alpha-linolenic acid supplementation in tris extender can improve frozen-thawed bull semen quality.

作者信息

Kaka A, Wahid H, Rosnina Y, Yimer N, Khumran A M, Behan A A, Ebrahimi M

机构信息

Department of Veterinary Clinical Studies, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Serdang, Malaysia; Sindh Agriculture University, Tando jam, Pakistan.

出版信息

Reprod Domest Anim. 2015 Feb;50(1):29-33. doi: 10.1111/rda.12445. Epub 2014 Nov 3.

DOI:10.1111/rda.12445
PMID:25366298
Abstract

The study was conducted to evaluate the effects of α-linolenic acid (ALA) on frozen-thawed quality and fatty acid composition of bull sperm. For that, twenty-four ejaculates obtained from three bulls were diluted in a Tris extender containing 0 (control), 3, 5, 10 and 15 ng/ml of ALA. Extended semen was incubated at 37°C for 15 min, to allow absorption of ALA by sperm cell membrane. The sample was chilled for 2 h, packed into 0.25-ml straws and frozen in liquid nitrogen for 24 h. Subsequently, straws were thawed and evaluated for total sperm motility (computer-assisted semen analysis), membrane functional integrity (hypo-osmotic swelling test), viability (eosin-nigrosin), fatty acid composition (gas chromatography) and lipid peroxidation (thiobarbituric acid-reactive substances (TBARS)). A higher (p < 0.05) percentage of total sperm motility was observed in ALA groups 5 ng/ml (47.74 ± 07) and 10 ng/ml (44.90 ± 0.7) in comparison with control (34.53 ± 3.0), 3 ng/ml (34.40 ± 2.6) and 15 ng/ml (34.60 ± 2.9). Still, the 5 ng/ml ALA group presented a higher (p < 0.05) percentage of viable sperms (74.13 ± 0.8) and sperms with intact membrane (74.46 ± 09) than all other experimental groups. ALA concentration and lipid peroxidation in post-thawed sperm was higher in all treated groups when compared to the control group. As such, the addition of 5 ng/ml of ALA to Tris extender improved quality of frozen-thawed bull spermatozoa.

摘要

本研究旨在评估α-亚麻酸(ALA)对公牛精子冻融质量和脂肪酸组成的影响。为此,从三头公牛采集的24份精液样本,分别用含有0(对照)、3、5、10和15 ng/ml ALA的Tris稀释液进行稀释。稀释后的精液在37°C下孵育15分钟,以使精子细胞膜吸收ALA。样本冷却2小时后,装入0.25 ml的细管中,并在液氮中冷冻24小时。随后,将细管解冻,并对精子的总活力(计算机辅助精液分析)、膜功能完整性(低渗肿胀试验)、活力(伊红-黑色素染色)、脂肪酸组成(气相色谱法)和脂质过氧化(硫代巴比妥酸反应物质(TBARS))进行评估。与对照组(34.53±3.0)、3 ng/ml组(34.40±2.6)和15 ng/ml组(34.60±2.9)相比,5 ng/ml(47.74±0.7)和10 ng/ml(44.90±0.7)的ALA组观察到更高(p<0.05)的总精子活力百分比。此外,5 ng/ml ALA组的活精子(74.13±0.8)和膜完整精子(74.46±0.9)百分比高于所有其他实验组。与对照组相比,所有处理组解冻后精子中的ALA浓度和脂质过氧化水平更高。因此,在Tris稀释液中添加5 ng/ml的ALA可提高冻融后公牛精子的质量。

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