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己酮可可碱可增加精子穿透去透明带仓鼠卵母细胞的能力,而不增加顶体反应。

Pentoxifylline increases sperm penetration into zona-free hamster oocytes without increasing the acrosome reaction.

作者信息

Morales P, Llanos M, Yovich J L, Cummins J M, Vigil P

机构信息

Unit of Reproduction and Development, Faculty of Biological Sciences, P. Catholic University of Chile, Santiago.

出版信息

Andrologia. 1993 Nov-Dec;25(6):359-62. doi: 10.1111/j.1439-0272.1993.tb02743.x.

Abstract

Several drugs have been used to stimulate human sperm motility, including 3-deoxy-adenosine, caffeine, and pentoxifylline. Pentoxifylline is an inhibitor of the phosphodiesterase and may stimulate sperm motility by increasing the intracellular levels of cAMP. In this study we have evaluated the effect of pentoxifylline in the outcome of the sperm penetration assay into zona-free hamster oocytes. Twenty-seven semen samples, obtained for diagnostic purposes, were used. After the motile sperm were selected by the swim-up technique, the samples were divided into two aliquots. One aliquot was incubated with 1 mg ml-1 of pentoxifylline at 37 degrees C, 5% CO2 for 30 min. The control aliquot was incubated with culture medium. The samples were then washed and resuspended in fresh, pentoxifylline-free medium, at a sperm concentration of 10 x 10(6) cells ml-1. One hundred microlitres of each sperm suspension was then deposited under oil and 30-40 zona-free hamster oocytes were added. After 6 h of gamete coincubation, the percentage of penetrated oocytes and the number of decondensed sperm heads were evaluated. The percentage of acrosome-reacted sperm was evaluated using the Pisum sativum lectin. The percentage of zona-free hamster oocytes penetrated was increased after pentoxifylline-treatment. The percentage of acrosome reacted sperm and the number of decondensed sperm heads per egg were not different between the control and the pentoxifylline-treated groups. The results suggest that the beneficial effect of pentoxifylline upon the sperm cells is not mediated by stimulation of the acrosome reaction.

摘要

几种药物已被用于刺激人类精子活力,包括3-脱氧腺苷、咖啡因和己酮可可碱。己酮可可碱是一种磷酸二酯酶抑制剂,可能通过增加细胞内cAMP水平来刺激精子活力。在本研究中,我们评估了己酮可可碱对精子穿透无透明带仓鼠卵母细胞试验结果的影响。使用了为诊断目的而获取的27份精液样本。通过上浮技术选择活动精子后,将样本分成两份。一份在37℃、5%二氧化碳条件下与1mg/ml己酮可可碱孵育30分钟。对照份与培养基孵育。然后将样本洗涤并重悬于新鲜的、不含己酮可可碱的培养基中,精子浓度为10×10⁶个细胞/ml。然后将每份精子悬液100微升置于油下,并加入30 - 40个无透明带仓鼠卵母细胞。配子共孵育6小时后,评估穿透卵母细胞的百分比和去浓缩精子头的数量。使用豌豆凝集素评估顶体反应精子的百分比。己酮可可碱处理后,无透明带仓鼠卵母细胞的穿透百分比增加。对照和己酮可可碱处理组之间,顶体反应精子的百分比和每个卵的去浓缩精子头数量没有差异。结果表明,己酮可可碱对精子细胞的有益作用不是通过刺激顶体反应介导的。

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