Franchi A M, Gonzalez E T, Gimeno M F, Gimeno A L
Prostaglandins. 1982 Dec;24(6):775-87. doi: 10.1016/0090-6980(82)90058-2.
The output of prostaglandin (PG) F and PGE-like material into the solution bathing uterine horns isolated from adult ovariectomized and immature rats under the influence of progesterone, was studied. The injection of progesterone (0.5; 1.0; 2.0 or 4.0 mg) 6 hours prior to sacrifice enhanced significantly the release of PGF-like substance without modifying that of PGE. The augmentation of PGF was detected as early as one hour after injecting 4.0 mg of progesterone and remained elevated at 2,4,6, 12 and 24 hours, following the treatment. Puromycin (50 mg/Kg), injected 6 hours before killing, failed to alter the release of PGF-like substance but clearly blocked the stimulating effect of the hormone. In addition, progesterone also enhanced significantly the release of PGF-like material by horns isolated from immature animals. The results suggest that progesterone receptors do not appear to be important for the described effect of the hormone because the preparations employed in the present study have a very small content of these receptors. Alternatively, it can be hypothesized that only a reduced number of progesterone receptors are sufficient for the action of the hormone augmenting the output of PGF-like material from the uterus.
研究了在孕酮作用下,成年去卵巢大鼠和未成年大鼠子宫角释放前列腺素(PG)F和PGE样物质的情况。处死前6小时注射孕酮(0.5、1.0、2.0或4.0毫克)可显著增强PGF样物质的释放,而不改变PGE的释放。注射4.0毫克孕酮后1小时即可检测到PGF的增加,且在处理后的2、4、6、12和24小时仍保持升高。处死前6小时注射嘌呤霉素(50毫克/千克)未能改变PGF样物质的释放,但明显阻断了激素的刺激作用。此外,孕酮还显著增强了从未成年动物分离出的子宫角释放PGF样物质的能力。结果表明,孕酮受体对于该激素的上述作用似乎并不重要,因为本研究中使用的制剂中这些受体的含量非常少。或者,可以假设仅减少数量的孕酮受体就足以使激素发挥作用,增加子宫中PGF样物质的输出。