Neal P, Baker T G, McNatty K P, Scaramuzzi R J
J Endocrinol. 1975 Apr;65(1):19-25. doi: 10.1677/joe.0.0650019.
The response of mouse ovaries maintained in organ culture to prostaglandin E-2 (PGE2) and prostaglandin F-2alpha (F2alpha) was assessed using quantitative histological and radioimmunoassay procedures. Prostaglandin E2 induced histological changes in the cultured follicles comparable to those induced by human chorionic gonadotrophin (HCG) and the increase in the number of oocytes undergoing preovulatory maturation over the control value was the same irrespective of the treatment (PGE2 alone, HCG alone, or PGE2+HCG). The amount of progesterone/ml of culture medium was also significantly higher with these preparations than in control cultures (about 125 ng/ml compared with 57 ng/ml). By contrast, 5 mug PGF2alpha/ml medium increased neither the number of oocytes undergoing maturation nor the concentration of progesterone in the culture medium. The latter increased when the dose of PGF2alpha was increased to 30 mug/ml, although the proportion of oocytes beyond the dictyate stage remained at the control level. There was no augmentation in the response (above the level for HCG alone) when HCG and PGF2alpha were added to the explant medium simultaneously. These results are discussed in terms of the possible mechanism of action of the various preparations.
采用定量组织学和放射免疫分析方法,评估了器官培养中维持的小鼠卵巢对前列腺素E-2(PGE2)和前列腺素F-2α(F2α)的反应。前列腺素E2在培养卵泡中诱导的组织学变化与人类绒毛膜促性腺激素(HCG)诱导的变化相当,且无论处理方式如何(单独使用PGE2、单独使用HCG或PGE2+HCG),经历排卵前成熟的卵母细胞数量相对于对照值的增加是相同的。与对照培养相比,这些处理组的每毫升培养基中孕酮的量也显著更高(约125纳克/毫升,而对照为57纳克/毫升)。相比之下,每毫升培养基中5微克的PGF2α既没有增加成熟卵母细胞的数量,也没有增加培养基中孕酮的浓度。当PGF2α的剂量增加到30微克/毫升时,后者有所增加,尽管处于双线期后的卵母细胞比例仍保持在对照水平。当将HCG和PGF2α同时添加到外植体培养基中时,反应没有增强(高于单独使用HCG的水平)。根据各种制剂可能的作用机制对这些结果进行了讨论。