首页> 外文期刊>Theriogenology >Cryopreservation and ensuing in vitro fertilization ability of boar spermatozoa from epididymides stored at 4degree C.
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Cryopreservation and ensuing in vitro fertilization ability of boar spermatozoa from epididymides stored at 4degree C.

机译:从4°C储存的附睾中冷冻保存公猪精子并确保其体外受精能力。

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摘要

The effect of storing boar epididymides at 4鳦 for a few days on post-thaw motility and in vitro fertilization (IVF) potential of spermatozoa recovered from these epididymides was studied. 20 pairs of epididymides were recovered from Large White boars at slaughter, and spermatozoa were immediately collected from one of each pair and frozen (controls). The remaining epididymides were cooled to 4?and stored for 1, 2 or 4 days after which spermatozoa were collected and frozen (experimental groups). In control samples, sperm motility was well maintained during the dilution procedure, but declined after freezing and thawing, while in the experimental groups sperm motility decreased immediately after collection (P<0.01). IVF experiments showed that penetration rates of spermatozoa from epididymides stored for 1, 2 or 4 days (12, 13 and 2% respectively) were lower (P<0.05) than those of control samples (40%). Oocyte penetration rate ability seemed to be reflected by acrosome integrity. The motility ofspermatozoa with the ability to penetrate oocytes from the 1- and 2-day stored groups did not differ from that of controls. The motility of spermatozoa lacking penetration ability gradually decreased as storage period increased. Control and experimentalgroups had high rates of monospermic penetration (64-90%) and male pronuclear formation (67-71%).
机译:研究了将野猪附睾在4℃下保存几天对解冻后运动性和从这些附睾中回收的精子体外受精(IVF)潜力的影响。从大白公猪宰杀中回收了20对附睾,并立即从每对中收集精子并冷冻(对照)。将其余的附睾冷却至4℃并保存1、2或4天,然后收集并冷冻精子(实验组)。在对照样品中,精子活力在稀释过程中保持良好,但在冷冻和融化后下降,而在实验组中,精子活力在收集后立即下降(P <0.01)。体外受精实验表明,从附睾中储存1、2或4天(分别为12%,13%和2%)的精子穿透率低于对照样品(40%)(P <0.05)。卵母细胞渗透率能力似乎由顶体完整性反映。具有1天和2天储存组的卵母细胞渗透能力的精子运动与对照组没有差异。缺乏穿透能力的精子活力随着贮藏期的增加而逐渐降低。对照组和实验组的单精子穿透率较高(64-90%),男性核形成率较高(67-71%)。

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