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转甲基化抑制剂对仓鼠精子顶体反应的抑制作用。

Inhibition of the hamster sperm acrosome reaction by transmethylation inhibitors.

作者信息

Meizel S

出版信息

J Exp Zool. 1981 Sep;217(3):443-6. doi: 10.1002/jez.1402170316.

Abstract

Two inhibitors of somatic cell transmethylation, homocysteine thiolactone (Hcy) and 3--deazadenosine (3--DZA), inhibited the acrosome reactions of hamster sperm in vitro. Hcy (250 microM) or 3--DZA (200 microM) inhibited acrosome reactions by approximately 30% after 4 hours of incubation with washed sperm in a capacitating medium containing epinephrine, taurine, and bovine serum albumin. Inhibition by 3--DZA decreased by 5 hours, but inhibition by Hcy did not. Incubation of sperm with the combination of both inhibitors inhibited acrosome reactions by nearly 60% at 4 hours, and did not appreciably decrease with time up to 5 hours. These results are the first to demonstrate that such inhibitors can interfere with the acrosome reaction and taken together with the effects of Hcy and 3--DZA on somatic cells, suggest that sperm protein and/or phospholipid transmethylation is/are involved in capacitation and/or the acrosome reaction.

摘要

两种体细胞转甲基化抑制剂,即同型半胱氨酸硫内酯(Hcy)和3 - 去氮腺苷(3 - DZA),在体外抑制了仓鼠精子的顶体反应。在含有肾上腺素、牛磺酸和牛血清白蛋白的获能培养基中,将洗涤后的精子与Hcy(250微摩尔)或3 - DZA(200微摩尔)孵育4小时后,它们对顶体反应的抑制率约为30%。3 - DZA的抑制作用在5小时后减弱,但Hcy的抑制作用没有减弱。将精子与两种抑制剂联合孵育,在4小时时对顶体反应的抑制率接近60%,并且在长达5小时的时间内没有明显下降。这些结果首次证明此类抑制剂可干扰顶体反应,并且结合Hcy和3 - DZA对体细胞的作用表明,精子蛋白和/或磷脂转甲基化参与了获能和/或顶体反应。

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