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Influence of semen processing technique on human sperm DNA integrity.

机译:精液加工技术对人类精子DNA完整性的影响。

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OBJECTIVES: To compare the effects of density-gradient centrifugation and swim-up technique on sperm DNA integrity. METHODS: Semen samples (n = 22) were obtained from consecutive nonazoospermic men presenting for infertility evaluation. Individual samples were divided into three aliquots (whole semen, density-gradient centrifugation, and swim-up) for subsequent analysis of sperm motility and DNA integrity. Sperm DNA integrity was evaluated by flow cytometry analysis of acridine orange-treated spermatozoa and expressed as the percentage of spermatozoa demonstrating denatured DNA. RESULTS: Mean sperm motility (+/-SEM) improved significantly after processing with two-layer density-gradient and swim-up compared with whole semen (65.6% +/- 4.0% and 73.0% +/- 3.0% versus 52.0% +/- 3.6%, respectively, P <0.005), with no significant difference in motility between Percoll-treated and swim-up-treated spermatozoa. In contrast, the percentage of spermatozoa with denatured DNA was reduced significantly in swim-up-treated but not in Percoll-treated spermatozoa compared with whole semen (4.8% +/- 1. 2% and 13.6% +/- 3.6% versus 10.1% +/- 2.3%, respectively, P <0. 0001). CONCLUSIONS: Although density-gradient centrifugation is comparable to swim-up technique in recovering spermatozoa with enhanced motility, spermatozoa recovered after swim-up possess higher DNA integrity. These data urge us to reexamine our current sperm processing techniques in order to minimize sperm DNA damage.
机译:目的:比较密度梯度离心法和游泳法对精子DNA完整性的影响。方法:从连续进行不育评估的无精子症男性中获取精液样本(n = 22)。将各个样品分成三等份(全精液,密度梯度离心和上清液),用于随后的精子活力和DNA完整性分析。通过流式细胞术分析a啶橙处理的精子来评估精子DNA的完整性,并表示为精子的百分数,表明变性DNA。结果:与全精液相比,采用两层密度梯度和上浮法处理后,平均精子活力(+/- SEM)显着提高(65.6%+/- 4.0%和73.0%+/- 3.0%vs 52.0%+ /-分别为3.6%,P <0.005),经Percoll处理和经游泳处理的精子的运动力无显着差异。相比之下,与全精液相比,经游泳处理的精子中具有变性DNA的精子百分比显着降低,但经Percoll处理的精子中的百分比未降低(4.8%+/-1。2%和13.6%+/- 3.6%对10.1)。 %+/- 2.3%,分别P <0。0001)。结论:虽然密度梯度离心法可与游动技术相媲美,以提高活力,但游动后恢复的精子具有更高的DNA完整性。这些数据促使我们重新检查我们目前的精子加工技术,以最大程度地减少精子DNA损伤。

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