Niemelä A O
J Steroid Biochem. 1986 Mar;24(3):709-13. doi: 10.1016/0022-4731(86)90847-2.
Regulation of avidin accumulation by prostaglandins (PGs) and their inhibitors was studied in chick oviduct organ culture. Avidin was induced neither by progesterone nor PGF2 alpha in the oviduct of immature chicks. By progesterone and PGs, a high avidin synthesis was induced when the chicks received diethylstilbestrol (DES) for 7 days. Enhanced avidin production was observed by PGF2 alpha, PGE1 and PGE2, whereas PGA2 and PGB2 had a slight inhibitory effect and PGA1 and PGB1 had no effect on avidin production. PGF2 alpha was most effective at a concentration of 10-20 micrograms/ml. The effects of progesterone and PGF2 alpha were not additive. Mefenamic acid, at concentrations of 40 and 60 micrograms/ml, inhibited 50 and 85%, respectively, of the avidin synthesis induced by progesterone, whereas the inhibition of the total protein synthesis was only 20%, and this only by the higher concentration of the drug. Tolfenamic and meclofenamic acid were also inhibitory in the case of progestin-induced avidin synthesis. These studies indicate that the PGs (F2 alpha, E1 and E2) might be involved in the avidin induction in the chick differentiated oviduct. The specific inhibition of the progesterone-dependent avidin synthesis by the PG inhibitors suggests that PGs may be connected with the progesterone action in the oviduct. We propose that the avidin synthesis by the chick oviduct might be considered as a model system for studying PG effects on the synthesis of a specific protein.
在鸡输卵管器官培养中研究了前列腺素(PGs)及其抑制剂对抗生物素蛋白积累的调节作用。在未成熟雏鸡的输卵管中,孕酮和前列腺素F2α均未诱导抗生物素蛋白的产生。当雏鸡接受己烯雌酚(DES)处理7天时,孕酮和PGs可诱导高抗生物素蛋白合成。观察到前列腺素F2α、前列腺素E1和前列腺素E2可增强抗生物素蛋白的产生,而前列腺素A2和前列腺素B2有轻微抑制作用,前列腺素A1和前列腺素B1对抗生物素蛋白的产生无影响。前列腺素F2α在浓度为10 - 20微克/毫升时最有效。孕酮和前列腺素F2α的作用不是相加的。甲芬那酸在浓度为40和60微克/毫升时,分别抑制孕酮诱导的抗生物素蛋白合成的50%和85%,而对总蛋白合成的抑制仅为20%,且仅在较高药物浓度时出现这种情况。托芬那酸和甲氯芬那酸对孕激素诱导的抗生物素蛋白合成也有抑制作用。这些研究表明,PGs(F2α、E1和E2)可能参与了鸡分化输卵管中抗生物素蛋白的诱导。PG抑制剂对孕酮依赖性抗生物素蛋白合成的特异性抑制表明,PGs可能与输卵管中孕酮的作用有关。我们提出,鸡输卵管的抗生物素蛋白合成可被视为研究PGs对特定蛋白质合成影响的模型系统。