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用射出的精子对大鼠和小鼠卵子进行体外受精以及能量来源对大鼠卵子体外受精的影响。

In vitro fertilization of rat and mouse eggs by ejaculated sperm and the effect of energy sources on in vitro fertilization of rat eggs.

作者信息

Tsunoda Y, Chang M C

出版信息

J Exp Zool. 1975 Jul;193(1):79-86. doi: 10.1002/jez.1401930107.

DOI:10.1002/jez.1401930107
PMID:1141844
Abstract

In vitro fertilization of rat and mouse eggs by ejaculated or epididymal spermatozoa in chemically defined media was studied. Penetration rates by ejaculated sperm was very low (0 to 8%) in the rat, but 11 to 41% of eggs were penetrated by ejaculated sperm in the mouse. The optimal concentration of sperm for in vitro fertilization appears to be similar whether ejaculated or epididymal sperm were used. The time of sperm penetration in the mouse eggs, however, was delayed for one-half to one hour when ejaculated sperm were used. The importance of sodium pyruvate, sodium lactate and glucose in the medium containing bovine serum albumin for in vitro fertilization of rat eggs was examined. When rat eggs in cumulus clot were exposed to epididymal sperm preincubated for five hours, the presence of sodium pyruvate, sodium lactate and glucose was found to play an important role. When exposed to non-incubated epididymal sperm sodium pyruvate could be omitted without much decline of the fertilization rate. When the denuded eggs were exposed to non-incubated sperm, penetration rates were very low (0 and 5%) in the absence of pyruvate. It appears that although lactate, pyruvate and glucose are all important for in vitro fertilization of rat eggs, pyruvate can be supplied by the follicular cells surrounding the eggs.

摘要

研究了在化学成分明确的培养基中,用射出的或附睾的精子对大鼠和小鼠卵子进行体外受精的情况。大鼠中,射出精子的穿透率非常低(0%至8%),但在小鼠中,11%至41%的卵子被射出精子穿透。无论使用射出的还是附睾的精子,体外受精的最佳精子浓度似乎相似。然而,当使用射出精子时,精子穿透小鼠卵子的时间延迟了半小时到一小时。研究了含有牛血清白蛋白的培养基中丙酮酸钠、乳酸钠和葡萄糖对大鼠卵子体外受精的重要性。当卵丘凝块中的大鼠卵子暴露于预先孵育5小时的附睾精子时,发现丙酮酸钠、乳酸钠和葡萄糖的存在起着重要作用。当暴露于未孵育的附睾精子时,可以省略丙酮酸钠而受精率没有太大下降。当裸卵暴露于未孵育的精子时,在没有丙酮酸盐的情况下穿透率非常低(0%和5%)。似乎虽然乳酸、丙酮酸和葡萄糖对大鼠卵子的体外受精都很重要,但丙酮酸可以由卵子周围的卵泡细胞提供。

相似文献

1
In vitro fertilization of rat and mouse eggs by ejaculated sperm and the effect of energy sources on in vitro fertilization of rat eggs.用射出的精子对大鼠和小鼠卵子进行体外受精以及能量来源对大鼠卵子体外受精的影响。
J Exp Zool. 1975 Jul;193(1):79-86. doi: 10.1002/jez.1401930107.
2
Penetration of hamster and pig zona-free eggs by boar ejaculated spermatozoa preincubated in vitro.体外预孵育的公猪射出精子对仓鼠和猪去透明带卵的穿透情况。
Int J Fertil. 1981;26(2):101-6.
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In vitro fertilization of hamster eggs by ejaculated or epididymal spermatozoa in the presence of male accessory secretions.在雄性附属性腺分泌物存在的情况下,用射出的或附睾精子对仓鼠卵进行体外受精。
J Exp Zool. 1977 Sep;201(3):445-9. doi: 10.1002/jez.1402010311.
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Sperm concentration dependency in the fertilization and zonae sperm binding properties of mouse eggs inseminated in vitro.体外受精的小鼠卵子受精及透明带精子结合特性中的精子浓度依赖性
J Exp Zool. 1976 Apr;196(1):27-37. doi: 10.1002/jez.1401960104.
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The importance of the presence of metabolizable sugars in a medium for in vitro fertilization of hamster eggs with postovulatory oviduct contents.可代谢糖在用于用排卵后输卵管内容物对仓鼠卵进行体外受精的培养基中的存在的重要性。
J Exp Zool. 1982 Apr 10;220(2):261-5. doi: 10.1002/jez.1402200215.
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The male factor in fertilization of rat eggs in vitro.
J Exp Zool. 1981 Sep;217(3):399-402. doi: 10.1002/jez.1402170310.
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Inhibition of in vitro fertilization of mouse eggs: 3-quinuclidinyl benzilate specifically blocks penetration of zonae pellucidae by mouse spermatozoa.抑制小鼠卵子的体外受精:二苯羟乙酸-3-喹咛环酯特异性阻断小鼠精子穿透透明带。
J Exp Zool. 1981 Apr;216(1):159-67. doi: 10.1002/jez.1402160117.
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Rate of egg penetration in vitro accelerated by T/t locus in the mouse.小鼠中T/t基因座加速体外卵子穿透率。
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Capacitation of hamster spermatozoa with the divalent cation chelators D-penicillamine, L-histidine, and L-cysteine in a protein-free culture medium.在无蛋白培养基中用二价阳离子螯合剂D-青霉胺、L-组氨酸和L-半胱氨酸使仓鼠精子获能。
Gamete Res. 1989 Jun;23(2):159-70. doi: 10.1002/mrd.1120230203.
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Purification of binder of sperm protein 1 (BSP1) and its effects on bovine in vitro embryo development after fertilization with ejaculated and epididymal sperm.精子蛋白1(BSP1)结合物的纯化及其对经射精精子和附睾精子受精后的牛体外胚胎发育的影响。
Theriogenology. 2016 Feb;85(3):540-54. doi: 10.1016/j.theriogenology.2015.09.044. Epub 2015 Oct 9.

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