Facultad de Ciencias Veterinarias, INITRA, Cátedra de Teriogenología, Universidad de Buenos Aires, Buenos Aires, Argentina.
Reprod Domest Anim. 2024 Sep;59(9):e14720. doi: 10.1111/rda.14720.
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.
据报道,在冷冻保存液中添加抗氧化剂可以改善精子解冻后的质量,并提高人工授精后的繁殖性能。因此,本研究的目的是评估在冷冻液中添加左旋肉碱和丙酮酸,或在解冻后添加到样本中,是否可以提高马精液的解冻后质量。因此,在实验 1 中,使用 EDTA-葡萄糖基础稀释液(含 20%卵黄和 5%二甲基甲酰胺)(EDTA 对照组)、脱脂奶基础稀释液(含 20%卵黄和 5%二甲基甲酰胺)(奶对照组)、添加 50mM 左旋肉碱和 10mM 丙酮酸的稀释液 1(EDTA-左旋肉碱-丙酮酸)和添加 50mM 左旋肉碱和 10mM 丙酮酸的稀释液 2(奶-左旋肉碱-丙酮酸)对种马精液进行冷冻保存。在实验 2 中,向使用稀释液 1 和 2(EDTA 对照组和奶对照组)冷冻保存的样本中添加 50mM 左旋肉碱和 10mM 丙酮酸。解冻后评估精子运动参数、DNA 碎片化、膜脂质过氧化、顶体状态和活力。在存在或不存在左旋肉碱和丙酮酸的情况下冷冻保存的样本之间,以及在解冻后添加这些成分的样本之间,大多数运动参数、DNA 碎片化、膜脂质过氧化、顶体状态和活力均无显著差异(p>0.05)。解冻后,在添加左旋肉碱和丙酮酸的奶基稀释液中冷冻保存的样本的平均速度更高(p<0.05),侧向头部位移幅度也更高(p<0.05)。在冷冻液中添加 50mM 左旋肉碱和 10mM 丙酮酸,无论是在冷冻前添加还是解冻后添加,都不会对精子造成损害;然而,它并没有改善马精子的活力、活力、顶体和 DNA 完整性,也没有降低解冻后的膜脂质过氧化。