Department of Clinical Studies - New Bolton Center, University of Pennsylvania School of Veterinary Medicine, Kennett Square, PA, 19348, USA.
Department of Clinical Studies - New Bolton Center, University of Pennsylvania School of Veterinary Medicine, Kennett Square, PA, 19348, USA.
Theriogenology. 2025 Jan 1;231:29-35. doi: 10.1016/j.theriogenology.2024.10.006. Epub 2024 Oct 9.
Intracytoplasmic sperm injection (ICSI) is a valuable assisted reproduction technology in clinical practice, especially when semen availability is limited. Since the number of sperm required per ICSI cycle is much less than the number of sperm available in a standard straw of frozen semen, refreezing semen at lower sperm concentrations could yield multiple straws for ICSI use. However, there is little data on the effect of sperm refreezing on ICSI outcomes, especially on the effect of extender used for refreezing. The objective of the present study was to evaluate the effect of refreezing extender on stallion sperm quality and embryo production after ICSI. Semen was frozen in a low egg yolk/glycerol/amide extender (Extender 1), then thawed, re-extended, and refrozen in each of three extenders. When sperm were refrozen in Extender 1, the cleavage rate was lower (P < 0.05) and the blastocyst development rate tended to be lower (P = 0.06) than for the once-frozen sperm. In contrast, when sperm were refrozen in high egg yolk/glycerol (Extender 2) or low egg yolk/milk/glycerol (Extender 3) extenders, cleavage and blastocyst development rates did not differ significantly from those for the once-frozen semen. Notably, sperm refrozen in Extender 1, which yielded the lowest ICSI outcomes, showed the highest sperm motility and viability, demonstrating that traditional measures of sperm quality were inadequate to assess the suitability of refrozen sperm for ICSI. In a follow-up experiment conducted to evaluate the effects of Extenders 1 and 3 when used for once-frozen semen, cleavage and blastocyst rates did not differ between extenders. In conclusion, the extender used to initially freeze stallion sperm may not significantly affect ICSI outcomes; however, the extender used for refreezing can significantly affect embryo production. Refrozen stallion semen can be effectively used for ICSI when low egg yolk/milk/glycerol extender is used for refreezing. Until further research is available, use of extenders without amides is recommended when refreezing stallion semen for ICSI.
胞浆内精子注射(ICSI)是临床实践中一种有价值的辅助生殖技术,特别是在精液供应有限时。由于每个 ICSI 周期所需的精子数量远少于标准冷冻精液吸管中的精子数量,因此可以降低精子浓度重新冷冻精液,以产生多个用于 ICSI 的吸管。然而,关于精子再冷冻对 ICSI 结果的影响,特别是对再冷冻用稀释液的影响的数据很少。本研究的目的是评估再冷冻稀释液对种马精子质量和 ICSI 后胚胎生产的影响。精子先用低卵黄/甘油/酰胺稀释液(稀释液 1)冷冻,然后解冻,再用三种稀释液中的每一种进行再扩展和再冷冻。当精子在稀释液 1 中再冷冻时,卵裂率较低(P<0.05),囊胚发育率也较低(P=0.06),而一次冷冻的精子则没有这种情况。相比之下,当精子在高卵黄/甘油(稀释液 2)或低卵黄/牛奶/甘油(稀释液 3)稀释液中再冷冻时,卵裂和囊胚发育率与一次冷冻的精液没有显著差异。值得注意的是,在再冷冻的精子中,精子活力和活力最高的精子是在稀释液 1 中再冷冻的,这表明传统的精子质量评估方法不足以评估再冷冻精子用于 ICSI 的适宜性。在后续的实验中,评估了稀释液 1 和 3 用于一次冷冻精液的效果,结果显示两种稀释液的卵裂率和囊胚率没有差异。总之,最初冷冻种马精子的稀释液可能不会显著影响 ICSI 结果;然而,用于再冷冻的稀释液会显著影响胚胎的产生。当使用低卵黄/牛奶/甘油稀释液再冷冻时,可有效用于 ICSI 的冷冻种马精子。在进一步的研究结果可用之前,建议在为 ICSI 再冷冻种马精液时使用不含酰胺的稀释液。