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首页> 外文期刊>Journal of Applied Ichthyology >Sperm motility and fertilizing ability of frozen spermatozoa of males (XY) and neomales (XX) of perch (Perca fluviatilis)
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Sperm motility and fertilizing ability of frozen spermatozoa of males (XY) and neomales (XX) of perch (Perca fluviatilis)

机译:鲈(Perca fluviatilis)的男性(XY)和新男性(XX)的冷冻精子的精子运动能力和受精能力

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摘要

The objective of this study was to freeze sperm of sex-reversed females (neomales) of perch and to test their fertilization ability. Sperm used was testicular (TSN), collected from females that have been inverted by means of externally administered 17-alpha methyltestosterone. Sperm collected from intact males (SSNM) of the same origin were used as control. Prior to freezing, both TSN and SSNM were diluted into 300 m m glucose solution at the ratio of 1 : 6 and DMSO was used as cryoprotectant (10% final concentration). Crypreservation was performed in 0.5 ml straws placed into a polystyrene box, three cm above the liquid nitrogen level for 10 min and thereafter transferred fully into liquid nitrogen. Samples were thawed in 40pC water bath for 8 s and used for the fertilization experiments. Spermatozoa concentration of fresh TSN and SSNM were estimated with 45.3 x 10# and 37.8 x 10# spermatozoa mlp#, respectively. Both sperm velocity and motility showed significant decreases in the TSN (134.6 om sp# and 12.8%) compared to the SSNM (203.2 om sp# and 94.7%) at 10 s after sperm activation. However, no differences were observed in terms of hatching rates between fresh TSN and SSNM (42.5 vs 49.3%) at fertilization densities of 12 x 10e spermatozoa per egg. Frozen/thawed SSNM exhibited similar hatching rates at 12 x 10e and 2.4 x 10e spermatozoa per egg (37.2% vs 29.1%). Hatching rates for frozen/thawed TSN were about 7.3% with 12 x 10e spermatozoa per egg and did not show any difference at 2.4 x 10e spermatozoa per egg (6.6%). Stripped sperm of normal perch can be successfully frozen. Squeezing of the testes is not a good method for collection of testicular sperm resulting into low velocity, motility and hatching rate. To understand the influences of neomales on sperm quality on reproductive success further studies should be performed addressing a full assay of motility and fertility criteria when using stripped sperm from normal males and neomales. Additionally, the results indicate that many of sex reversed perch neomales are not able to release sperm and that for further studies some well spermiating neomales must to be selected.
机译:这项研究的目的是冻结鲈鱼性别反转雌性(线虫)的精子并测试其受精能力。所使用的精子是睾丸(TSN),从通过外部给药的17-α甲基睾丸激素倒转的雌性体内收集。从相同来源的完整雄性(SSNM)收集的精子用作对照。冷冻之前,将TSN和SSNM均以1:6的比例稀释到300 m m葡萄糖溶液中,并将DMSO用作冷冻保护剂(最终浓度为10%)。在置于液氮水平三厘米处的聚苯乙烯盒中的0.5 ml吸管中进行低温保存10分钟,然后将其完全转移至液氮中。将样品在40pC水浴中融化8 s,用于施肥实验。新鲜TSN和SSNM的精子浓度分别估计为45.3 x 10#和37.8 x 10#精子mlp#。精子活化后10 s,与SSNM(203.2 om sp#和94.7%)相比,TSN的精子速度和运动力均显着下降(134.6 om sp#和12.7%)。但是,在每个鸡蛋12 x 10e精子的受精密度下,新鲜TSN和SSNM之间的孵化率没有差异(42.5对49.3%)。冷冻/解冻的SSNM在每个鸡蛋12 x 10e和2.4 x 10e精子时显示出相似的孵化率(37.2%对29.1%)。冷冻/解冻的TSN的孵化率约为7.3%,每个鸡蛋含12 x 10e精子,而每个鸡蛋2.4 x 10e精子(6.6%)则无差异。正常鲈鱼的精子剥落可以成功冷冻。挤压睾丸不是收集睾丸精子的好方法,因为睾丸精子的速度,运动性和孵化率低。为了了解新雄性对精子质量对生殖成功的影响,当使用从正常雄性和新雄性中提取的精子时,应进行进一步的研究,以对运动性和生育力标准进行全面测定。此外,结果表明,许多性反转的鲈鱼新男性无法释放精子,并且有待进一步研究,以选择一些精子繁殖的新男性。

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