19‐去甲雄烯二酮(4‐estene‐3,17‐dione)抑制猪卵母细胞体外成熟

S. Daniel, M. Khalil, D. Armstrong
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引用次数: 11

摘要

最近的研究表明,19-去甲雄烯二酮是猪卵泡液的主要甾体成分;然而,对其在卵泡功能调节中的作用知之甚少。本研究旨在探讨19-去甲雄烯二酮对猪卵母细胞体外成熟的影响。从中等(直径3 - 6毫米)大小的青春期前猪卵泡中分离卵母细胞-卵丘复合物,在有或没有二丁基环AMP ((Bu)2cAMP, 1毫米)和有或没有睾酮(5 × 10−7米)或19-去甲雄烯二酮(5 × 10−7米)的培养基中孵育12小时。仅在培养基中,70.8%的卵母细胞自发恢复减数分裂,这表明发生了生发囊泡破裂。(Bu)2cAMP抑制卵母细胞成熟(44.6%成熟)。虽然类固醇单独影响成熟,但睾酮和19-去甲雄烯二酮都增强了(Bu)2cAMP的作用(分别为22.5%和19.6%)。睾酮和19-去甲雄烯二酮对(Bu) 2camp抑制的卵母细胞成熟的影响呈剂量依赖性,两种激素的作用无显著差异。19-去甲雄烯二酮的作用是可逆的,并且依赖于完整积云的存在。羟氟他胺(SCH-16423)是一种已知能阻断雄激素受体的非甾体化合物,它能消除睾丸激素和19-去甲雄烯二酮对生发囊泡破裂的影响,表明这些类固醇的作用确实是雄激素性的。本研究结果提示,19-去甲雄烯二酮可能在调节猪卵母细胞成熟过程中具有重要的生理意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
19‐Norandrostenedione (4‐estrene‐3,17‐dione) Inhibits Porcine Oocyte Maturation In Vitro
Recent work has shown that 19-norandrostenedione is a major steroidal component of porcine follicular fluid; however, little is known about its role(s) in the regulation of follicular function. This study was designed to examine the effect of 19-norandrostenedione on porcine oocyte maturation in vitro. Oocyte-cumulus complexes were isolated from medium (3–6-mm diameter)-sized prepubertal pig follicles and incubated for 12 h in medium with or without dibutyryl cyclic AMP ((Bu)2cAMP, 1 mM) with or without testosterone (5 x 10−7 M) or 19-norandrostenedione (5 x 10−7 M). In medium alone, 70.8% of oocytes spontaneously resumed meiosis as evidenced by the occurrence of germinal vesicle breakdown. Oocyte maturation was inhibited by (Bu)2cAMP (44.6% of oocytes matured). Although neither steroid alone affected maturation, both testosterone and 19-norandrostenedione enhanced the effect of (Bu)2cAMP (22.5 and 19.6%, respectively, resumed meiosis). The effects of testosterone and 19-norandrostenedione on (Bu)2cAMP-inhibited oocyte maturation were dose dependent and there was no significant difference between the actions of the steroids. The effect of 19-norandrostenedione was reversible and dependent on the presence of an intact cumulus. Hydroxyflutamide (SCH-16423), a nonsteroidal compound known to block androgen receptors, abolished the effects of both testosterone and 19-norandrostenedione on germinal vesicle breakdown, indicating that the actions of these steroids are truly androgenic. The results of this study suggest that 19-norandrostenedione may be of physiological importance in the regulation of porcine oocyte maturation.
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