Effect of alterations in follicular steroidogenesis on the nuclear and cytoplasmic maturation of ovine oocytes.

J C Osborn, R M Moor, I M Crosby
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Abstract

The effects of inhibitors of follicular steroidogenesis on biochemical changes occurring in oocytes maturing in vitro were studied using radiolabelling and polyacrylamide gel electrophoresis. These effects were correlated with previously investigated developmental abnormalities induced by the same inhibitors. The most severe effects were generated by inhibition of 17 alpha-hydroxylase with the drug SU10603 which resulted in a greatly increased ratio of progesterone to testosterone and oestrogen. Such treatment halved the rate of meiotic maturation. Treated oocytes were analysed individually on SDS-PAGE gels and quantitative analysis showed that the drug had induced synthetic abnormalities even in those oocytes that resumed meiosis. This conclusion was confirmed by separation of oocyte proteins on two-dimensional gels. The effects of SU were reduced by delaying addition of the drug until 6h after the beginning of maturation but were not alleviated by the addition of exogenous oestrogen to the culture medium. When oocytes from SU-treated follicles were transferred to inseminated, recipient ewes and recovered 24h later, two-dimensional electrophoresis again revealed abnormalities in their protein synthetic patterns. Almost total abolition of steroid secretion by aminoglutethimide (AG) had much less effect on oocyte protein synthesis, although the proportion of oocytes maturing was reduced from 65% to 46%. The aromatase inhibitor, androstatriendione (AST) although eliminating follicular oestrogen secretion, had no effect on the rate of maturation and very little effect on protein synthesis. These results correlate well with the effects of steroid inhibitors on fertilization and early cleavage.

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卵泡甾体生成改变对绵羊卵母细胞核和细胞质成熟的影响。
采用放射性标记和聚丙烯酰胺凝胶电泳技术研究了卵泡甾体生成抑制剂对体外成熟卵母细胞生化变化的影响。这些影响与先前研究的由相同抑制剂引起的发育异常相关。SU10603对17 α -羟化酶的抑制作用最为严重,导致孕酮与睾酮和雌激素的比例显著升高。这样的处理使减数分裂成熟的速度减半。在SDS-PAGE凝胶上对处理后的卵母细胞进行单独分析,定量分析表明,即使在恢复减数分裂的卵母细胞中,药物也引起了合成异常。卵母细胞蛋白在二维凝胶上的分离证实了这一结论。将SU的作用推迟到成熟开始后6小时,可以降低SU的作用,但在培养基中添加外源雌激素并不能减轻SU的作用。当将su处理过的卵泡中的卵母细胞转移到受精卵受体母羊体内并在24小时后恢复时,二维电泳再次显示其蛋白质合成模式异常。氨酰硫胺(AG)几乎完全消除了类固醇分泌,但对卵母细胞蛋白质合成的影响要小得多,尽管成熟卵母细胞的比例从65%降至46%。芳香酶抑制剂雄甾烯二酮(AST)虽然能消除卵泡雌激素分泌,但对成熟速度没有影响,对蛋白质合成的影响也很小。这些结果与类固醇抑制剂对受精和早期卵裂的影响密切相关。
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