Freezing-free preservation of human spermatozoa--a pilot study.

Jonathan M Riel, Thomas T F Huang, Monika A Ward
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引用次数: 4

Abstract

This study tested a method for maintaining human spermatozoa without freezing for subsequent use in intracytoplasmic sperm injection (ICSI). We demonstrated that human sperm stored in electrolyte-free solution maintain their motility and viability for at least 4 and 6 weeks, respectively. We also have shown that preserved spermatozoa are fully functional in ICSI. Sperm chromosome analysis after injection of human sperm into mouse oocytes revealed that two weeks of storage does not negatively affect sperm DNA integrity. A mouse model was used to analyze the ability of preserved sperm to participate in normal embryogenesis. Mouse sperm preserved in electrolyte-free solution in a similar manner as human sperm maintained motility for up to 3 weeks. When mouse spermatozoa stored for 1 week were injected into the oocytes by ICSI, they yielded normal blastoctysts and normal viable fetuses. The results of the study bear significance for human assisted reproduction technologies (ART) and provide clinicians and infertile patients with a new method that can simplify sperm preparation for ICSI, assisting men who are unable to provide semen on the day of assisted fertilization.

人类精子的无冷冻保存——初步研究。
本研究测试了一种不冷冻保存人类精子的方法,用于后续的卵胞浆内单精子注射(ICSI)。我们证明,储存在无电解质溶液中的人类精子分别保持至少4周和6周的活力和活力。我们也证明了在ICSI中保存的精子具有完全的功能。将人类精子注射到小鼠卵母细胞后,精子染色体分析显示,两周的储存不会对精子DNA完整性产生负面影响。用小鼠模型分析保存精子参与正常胚胎发生的能力。小鼠精子以与人类精子类似的方式保存在无电解质溶液中,最长可保持3周的活力。将储存1周的小鼠精子通过ICSI注射到卵母细胞中,产生正常的囊胚和正常的活胎。本研究结果对人类辅助生殖技术(ART)具有重要意义,为临床医生和不孕症患者提供了一种简化ICSI精子准备的新方法,为辅助受精当天无法提供精液的男性提供帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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