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将人类精子显微注射到仓鼠卵的卵周隙中:与人类精子穿透无透明带仓鼠卵的比较。

Microinjection of human sperm into perivitelline space of hamster eggs: comparison with zona-free hamster egg penetration of human sperm.

作者信息

Chen S U, Yang Y S, Ho H N, Hwang J L, Hong T S, Lin H R, Huang S C, Lee T Y

机构信息

Department of Obstetrics/Gynecology, College of Medicine, National Taiwan University, Taipei, Republic of China.

出版信息

Arch Androl. 1993 May-Jun;30(3):201-7. doi: 10.3109/01485019308987757.

Abstract

Micromanipulation of human sperm and oocyte has been utilized to facilitate fertilization of those patients with male factor due to oligoasthenospermia or those patients with repeated fertilization failure in an in vitro fertilization (IVF) program. Before manipulating human gametes, one needs experience with animal models. Our objective was to perform subzonal insertion of human sperm into hamster eggs and to compare the result with that of sperm penetration assay (SPA) using zona-free hamster eggs. Semen samples were obtained from 15 fertile donors with normal semen analysis and the motile sperm were collected by swim-up procedure. Microinjection was performed by injecting a varied number of sperm into the perivitelline space of 222 hamster eggs pretreated with sucrose solution (0.1 M). The rate of damage of eggs during microinjection was 7.2% (16/222). The rates of penetration in the microinjection group were 5.1% (4/79) for 1-5 sperm injected, 10.9% (11/101) for 6-10 sperm injected, and 11.5% (3/26) for 11-15 sperm injected. The average rate of penetration per egg was 8.7% (18/206), and the polyspermic rate was 11.1% (2/18). Simultaneously SPA was performed in each sample of semen as a positive control, and the average rate of penetration of SPA was 51.4% (108/210). The rate of penetration in the microinjection group was significantly smaller (p < .05) than that in the SPA group. Whether the penetration rate and polyspermic rate in a hamster model reflect similar results in human oocyte requires further investigation. However, the hamster egg provides an ideal model to develop a micromanipulation technique for human beings.

摘要

人类精子和卵母细胞的显微操作已被用于帮助那些因少弱精子症而存在男性因素的患者或那些在体外受精(IVF)程序中反复受精失败的患者实现受精。在对人类配子进行操作之前,需要有动物模型的经验。我们的目标是将人类精子亚 zona 插入仓鼠卵,并将结果与使用无透明带仓鼠卵的精子穿透试验(SPA)的结果进行比较。精液样本取自 15 名精液分析正常的可育供者,通过上浮法收集活动精子。通过将不同数量的精子注射到用蔗糖溶液(0.1 M)预处理的 222 个仓鼠卵的卵周间隙中来进行显微注射。显微注射过程中卵的损伤率为 7.2%(16/222)。显微注射组中,注射 1 - 5 个精子时的穿透率为 5.1%(4/79),注射 6 - 10 个精子时为 10.9%(11/101),注射 11 - 15 个精子时为 11.5%(3/26)。每个卵的平均穿透率为 8.7%(18/206),多精受精率为 11.1%(2/18)。同时,对每个精液样本进行 SPA 作为阳性对照,SPA 的平均穿透率为 51.4%(108/210)。显微注射组的穿透率明显低于 SPA 组(p <.05)。仓鼠模型中的穿透率和多精受精率是否反映人类卵母细胞的类似结果需要进一步研究。然而,仓鼠卵为开发人类显微操作技术提供了一个理想模型。

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