Pre- and Post-Thaw Addition of L-Carnitine and Pyruvate: Effect on Stallion Sperm Parameters.

IF 1.6 3区 农林科学 Q2 AGRICULTURE, DAIRY & ANIMAL SCIENCE Reproduction in Domestic Animals Pub Date : 2024-09-01 DOI:10.1111/rda.14720
Mariana Caldevilla, Alejandro Ferrante, Débora M Neild
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Abstract

The addition of antioxidants to cryopreservation media reportedly improves sperm post-thaw quality and reproductive performance after artificial insemination. Therefore, the objectives of this study were to evaluate if the addition of L-carnitine and pyruvate to freezing media, or their addition to samples after thawing, improves the post-thaw quality of equine spermatozoa. Thus, in Experiment 1, stallion semen samples were cryopreserved in: (1) EDTA-glucose-based extender with 20% egg yolk and 5% dimethylformamide (EDTA control); (2) skim milk-based extender with 20% egg yolk and 5% dimethylformamide (milk control); (3) Extender 1 supplemented with 50 mM L-carnitine and 10 mM pyruvate (EDTA-carnitine-pyruvate); and (4) Extender 2 supplemented with 50 mM L-carnitine and 10 mM pyruvate (milk-carnitine-pyruvate). In Experiment 2, 50 mM L-carnitine and 10 mM pyruvate were added post-thaw to samples cryopreserved with extenders 1 and 2 (EDTA control and milk control). Sperm kinematic parameters, DNA fragmentation, membrane lipid peroxidation, acrosome status and viability were evaluated after thawing. No significant differences (p > 0.05) were observed for most of the kinematic parameters, DNA fragmentation, membrane lipid peroxidation, acrosome status and viability of spermatozoa, between the samples frozen in the presence or absence of L-carnitine and pyruvate, nor between the samples after the post-thaw addition of these components. A higher (p < 0.05) mean velocity and higher (p < 0.05) amplitude of lateral head displacement were observed in the samples frozen in the milk-based extender with the addition of L-carnitine and pyruvate after thawing. The addition of 50 mM L-carnitine and 10 mM pyruvate, either to the freezing extenders or after thawing, was not deleterious for sperm; however, it did not improve equine sperm motility, viability, acrosome and DNA integrity, nor decrease membrane lipid peroxidation after thawing.

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解冻前和解冻后添加左旋肉碱和丙酮酸:对种马精子参数的影响。
据报道,在冷冻保存介质中添加抗氧化剂可提高精子解冻后的质量和人工授精后的繁殖性能。因此,本研究的目的是评估在冷冻培养基中添加左旋肉碱和丙酮酸,或在解冻后向样本中添加这两种物质是否能提高马精子的解冻后质量。因此,在实验 1 中,种马精液样本在以下培养基中冷冻保存:(1) 以乙二胺四乙酸(EDTA)-葡萄糖为基础,添加 20% 蛋黄粉和 5% 二甲基甲酰胺(EDTA 对照组);(2) 以脱脂奶为基础,添加 20% 蛋黄粉和 5% 二甲基甲酰胺(牛奶对照组);(3) 添加 50 毫摩尔左旋肉碱和 10 毫摩尔丙酮酸的扩展剂 1(乙二胺四乙酸-肉碱-丙酮酸);以及 (4) 添加 50 毫摩尔左旋肉碱和 10 毫摩尔丙酮酸的扩展剂 2(牛奶-肉碱-丙酮酸)。在实验 2 中,使用扩展剂 1 和扩展剂 2(EDTA 对照组和牛奶对照组)冷冻保存的样本在解冻后加入 50 mM 左旋肉碱和 10 mM 丙酮酸。解冻后对精子运动参数、DNA 断裂、膜脂过氧化、顶体状态和存活率进行了评估。在有左旋肉碱和丙酮酸或没有左旋肉碱和丙酮酸的情况下冷冻的样本之间,以及在解冻后添加这些成分的样本之间,精子的大多数运动参数、DNA片段、膜脂过氧化、顶体状态和存活率均无明显差异(p > 0.05)。较高(p
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来源期刊
Reproduction in Domestic Animals
Reproduction in Domestic Animals 农林科学-奶制品与动物科学
CiteScore
3.00
自引率
5.90%
发文量
238
审稿时长
4-8 weeks
期刊介绍: The journal offers comprehensive information concerning physiology, pathology, and biotechnology of reproduction. Topical results are currently published in original papers, reviews, and short communications with particular attention to investigations on practicable techniques. Carefully selected reports, e. g. on embryo transfer and associated biotechnologies, gene transfer, and spermatology provide a link between basic research and clinical application. The journal applies to breeders, veterinarians, and biologists, and is also of interest in human medicine. Interdisciplinary cooperation is documented in the proceedings of the joint annual meetings. Fields of interest: Animal reproduction and biotechnology with special regard to investigations on applied and clinical research.
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