Garcia M, Rochefort H
Steroids. 1977 Jan;29(1):111-26. doi: 10.1016/0039-128x(77)90114-3.
In the immature rat uterus, occupation of the androgen and estrogen receptor sties after injection of 5 alpha dihydrotestosterone (DHT = 17beta - hydroxy-5alpha-androstan-3-one) were compared to the biological responses induced by the androgen on protein synthesis. Injection of 100 mug DHT induced a maximal occupation of androgen receptor sites (RA) but was totally ineffective in translocating the estrogen receptor sites and in increasing general protein synthesis. Conversely, high doses of androgen (greater than or equal to 3 mg) translocated the estrogen receptor (RE) and stimulated general protein synthesis. In addition, these high doses induced a specific uterine protein undistinguishable from that induced by estradiol treatment (IP). These results strongly suggest that the uterotrophic response of the uterus to androgen is correlated with the nuclear transreceptor which is present in much smaller amounts.
在未成熟大鼠子宫中,将注射5α-二氢睾酮(DHT = 17β-羟基-5α-雄甾烷-3-酮)后雄激素和雌激素受体位点的占据情况与雄激素对蛋白质合成诱导的生物学反应进行了比较。注射100μg DHT可诱导雄激素受体位点(RA)的最大占据,但在转运雌激素受体位点和增加总体蛋白质合成方面完全无效。相反,高剂量雄激素(≥3mg)可转运雌激素受体(RE)并刺激总体蛋白质合成。此外,这些高剂量诱导产生一种与雌二醇处理诱导的子宫特异性蛋白(IP)无法区分的蛋白。这些结果强烈表明,子宫对雄激素的子宫营养反应与含量少得多的核转受体相关。