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首页> 外文期刊>Journal of reproduction and fertility >Potassium ions modulate expression of mouse sperm fertilizing ability, acrosome reaction and hyperactivated motility in vitro
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Potassium ions modulate expression of mouse sperm fertilizing ability, acrosome reaction and hyperactivated motility in vitro

机译:钾离子调节体外小鼠精子受精能力,顶体反应和超活化运动的表达

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Summary. In K+-free medium, epididymal sperm suspensions, whether washed free of epididymally-derived K+ or not, were unable to penetrate washed cumulus masses; some penetration of zona-free eggs was obtained with unwashed sperm suspensions, while washed samples were generally non-fertilizing. Within 5 min of K+ introduction, however, spermatozoa were able to fertilize intact eggs rapidly and synchronously, indicating that K+ was not required for capacitation. Measurements of extracellular K+ concentrations in these experiments indicate that 0·1–0·15 mm-K+ is sufficient to support sperm:egg fusion, but concentrations >0·15 mm are required for penetration of cumulus-intact eggs. When medium of normal osmolality (318 mosmol) but elevated K+/Na+ ratio (27·7 mm/125 mm) was compared with control medium (2·7/150), the former promoted lower rates of penetration after both 30 and 120 min preincubation (8 and 10%, respectively) than those obtained with control medium (45 and 95%). Upon reduction to the ratio in control media, however, the fertilizing potential of these suspensions was equivalent to control samples: relatively slow and asynchronous penetration after 30 min preincubation (50%) and rapid, synchronous penetration after 120 min (92%). Thus there was no evidence of a shortening of sperm capacitation time, but rather a suppression of fertilizing potential in the presence of elevated K+. Uterine sperm samples recovered shortly after mating gave similar results when tested in these media 30 and 120 min after release from the male tract. Preincubation of epididymal samples in high K+ (27-7 mm) hyperosmolal media (368 mosmol) for 30 min significantly shortened sperm capacitation as shown by rapid penetration of intact eggs (94%) after reduction in osmolality, but this appeared to be a non-specific effect; high Na+ (175 mm) hyperosmolal medium had a similar effect (98% of eggs fertilized). Acrosome loss and hyperactivated motility were significantly lower in media with very low or very high K+ concentrations but, after alteration to control medium values, increased to levels similar to those obtained with control samples. It is proposed that the relatively high K+ concentrations found in female tract fluids ( ~ 20–30 mm) may serve to modulate fertilizing potential of spermatozoa in vivo.
机译:概要。在无K +的培养基中,附睾的精子悬浮液,无论是否经过附睾来源的K +冲洗,都无法渗透到冲洗的卵丘块中。未清洗的精子悬浮液可渗透到一些无盐卵,而清洗后的样品通常不受精。然而,在引入K +的5分钟内,精子能够快速而同步地使完整卵受精,这表明获能不需要K +。在这些实验中对细胞外K +浓度的测量表明,0·1–0·15 mm-K +足以支持精子:卵的融合,但要穿透完整卵卵则需要大于0·15 mm的浓度。当将正常渗透压(318摩尔)但K + / Na +比(27·7 mm / 125 mm)升高的介质与对照介质(2·7/150)进行比较时,前者在30和120分钟后促进较低的渗透率预孵育(分别为8%和10%),而不是对照培养基(分别为45和95%)。但是,降低至对照培养基中的比例后,这些悬浮液的受精潜力与对照样品相同:预孵育30分钟后相对缓慢且异步渗透(50%),120分钟后快速同步渗透(92%)。因此,没有证据显示精子获能时间缩短,而是在钾离子浓度升高时抑制了受精潜力。交配后不久回收的子宫精子样本在从雄性管道释放后的30和120分钟内在这些培养基中进行测试时,得到的结果相似。附睾样品在高K +(27-7 mm)高渗介质(368 mosmol)中预孵育30分钟可显着缩短精子获能能力,这是渗透压降低后完整卵(94%)的快速渗透所显示的,但这似乎是不可行的。特效;高Na +(175毫米)高渗性介质具有类似的效果(98%的受精卵)。在极低或非常高的K +浓度的培养基中,顶体损失和过度活化的运动显着降低,但在改变为对照培养基值后,其升高至与对照样品相似的水平。有人认为,女性尿液中的相对较高的K +浓度(〜20–30 mm)可能用于调节体内精子的受精潜力。

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