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使用四种不同商业介质进行密度梯度离心后,对人类精子的正常形态、DNA片段化及透明质酸结合能力的评估。

Evaluation of normal morphology, DNA fragmentation, and hyaluronic acid binding ability of human spermatozoa after using four different commercial media for density gradient centrifugation.

作者信息

Lee Dayong, Jee Byung Chul

机构信息

Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam, Korea.

出版信息

Clin Exp Reprod Med. 2019 Mar;46(1):8-13. doi: 10.5653/cerm.2019.46.1.8. Epub 2019 Mar 1.

Abstract

OBJECTIVE

Density gradient centrifugation (DGC) is frequently used to isolate high-motility fractions of spermatozoa. We compared the efficacy of four DGC media in terms of the percentage of morphologically normal spermatozoa, DNA fragmentation level, and hyaluronic acid (HA) binding ability.

METHODS

Thirty men with a total motile spermatozoa count >80 million participated. Semen samples were divided into four aliquots, which were processed using PureSperm, PureCeption, Sidney, and SpermGrad media, respectively. The DNA fragmentation level was measured using the Halosperm assay kit and HA binding ability was measured using the HBA assay kit.

RESULTS

The mean percentage of morphologically normal spermatozoa was significantly enhanced after DGC using all four media (10.3%, 9.9%, 9.8%, and 10.7%, respectively; p<0.05 for each when compared with 6.9% in raw semen). The DNA fragmentation level was significantly reduced after DGC using PureSperm, PureCeption, and SpermGrad media (6.0%, 6.5%, and 4.9%, respectively; p<0.05 for each when compared with 11.2% in raw semen), but not after DGC using Sidney media (8.5%, p>0.05). HA binding ability did not change after DGC using any of the four media.

CONCLUSION

The four media were equally effective for obtaining a sperm fraction with highly motile, morphologically normal sperm. Pure-Sperm, PureCeption, and SpermGrad media were equally effective for acquiring a sperm fraction with less DNA fragmentation.

摘要

目的

密度梯度离心法(DGC)常用于分离高活力精子部分。我们比较了四种DGC培养基在形态正常精子百分比、DNA片段化水平和透明质酸(HA)结合能力方面的效果。

方法

30名总活动精子数>8000万的男性参与。精液样本分为四个等分试样,分别使用PureSperm、PureCeption、Sidney和SpermGrad培养基进行处理。使用Halosperm检测试剂盒测量DNA片段化水平,使用HBA检测试剂盒测量HA结合能力。

结果

使用所有四种培养基进行DGC后,形态正常精子的平均百分比均显著提高(分别为10.3%、9.9%、9.8%和10.7%;与未处理精液中的6.9%相比,每种培养基处理后的p值均<0.05)。使用PureSperm、PureCeption和SpermGrad培养基进行DGC后,DNA片段化水平显著降低(分别为6.0%、6.5%和4.9%;与未处理精液中的11.2%相比,每种培养基处理后的p值均<0.05),但使用Sidney培养基进行DGC后未降低(8.5%,p>0.05)。使用四种培养基中的任何一种进行DGC后,HA结合能力均未改变。

结论

这四种培养基在获得具有高活力、形态正常精子的精子部分方面同样有效。Pure-Sperm、PureCeption和SpermGrad培养基在获得DNA片段化较少的精子部分方面同样有效。

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