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体外获能过程中人类精子运动的变化。

Changes in human sperm motion during capacitation in vitro.

作者信息

Morales P, Overstreet J W, Katz D F

机构信息

Department of Obstetrics and Gynecology, University of California, Davis 95616.

出版信息

J Reprod Fertil. 1988 May;83(1):119-28. doi: 10.1530/jrf.0.0830119.

Abstract

Spermatozoa from 10 fertile donors and from 10 patients with infertile marriages were washed and centrifuged (time zero, T0), and incubated in vitro in capacitation media for 6 h (T6), or 24 h (T24). At each time individual spermatozoa were classified as being morphologically normal or abnormal, and their movement characteristics were determined using high-speed videomicrography. Zona-free hamster oocytes were added to the T24 sperm suspensions. At all times, morphologically normal spermatozoa from donors and patients swam faster and had greater rolling frequency, flagellar beat frequency and amplitude than did abnormally shaped cells. Morphologically normal spermatozoa from donors exhibited a significant change in their movement pattern at T6. This change, which resembles hyperactivation in other species, was characterized by higher values of amplitude of lateral head displacement, and lower values of linearity, beat frequency and flagellar curvature ratio. In contrast, normal spermatozoa from patients showed only a decrease in straight line velocity at T6, with no other significant changes in movement characteristics. No changes in sperm movement could be demonstrated for the abnormal cells in either group of subjects. In sperm suspensions from donors and patients examined at T24, sperm vigour declined regardless of the morphological type. Spermatozoa from all 10 donors were able to penetrate the zona-free hamster oocytes, but spermatozoa from 5 of the 10 patients failed to penetrate oocytes. Correlations between hamster oocyte penetration and indicators of sperm vigour were demonstrated only for spermatozoa of patients.

摘要

对来自10名有生育能力的供体以及10名不育婚姻患者的精子进行洗涤和离心(时间零点,T0),然后在体外获能培养基中孵育6小时(T6)或24小时(T24)。在每个时间点,将单个精子分类为形态正常或异常,并使用高速摄像显微镜确定其运动特征。将无透明带仓鼠卵母细胞添加到T24精子悬液中。在所有时间点,供体和患者的形态正常精子比形态异常的细胞游动速度更快,滚动频率、鞭毛摆动频率和振幅更大。供体的形态正常精子在T6时运动模式发生显著变化。这种变化类似于其他物种的超激活,其特征是头部侧向位移幅度值较高,而直线性、摆动频率和鞭毛曲率比值较低。相比之下,患者的正常精子在T6时仅直线速度下降,运动特征无其他显著变化。两组受试者中形态异常的细胞均未表现出精子运动的变化。在T24检查的供体和患者的精子悬液中,无论形态类型如何,精子活力均下降。10名供体的所有精子均能穿透无透明带仓鼠卵母细胞,但10名患者中有5名患者的精子未能穿透卵母细胞。仅在患者精子中证明了仓鼠卵母细胞穿透与精子活力指标之间的相关性。

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