Dhar J D, Mishra R, Setty B S
Division of Endocrinology, Central Drug Research Institute, Lucknow, India.
Endocr Res. 1998 May;24(2):159-69. doi: 10.1080/07435809809135525.
Recent studies have indicated that estrogen has a stimulatory influence on the male reproductive tract. Evidence includes the presence of measurable levels of estrogen in the circulation, retention of exogenous estrogen, and presence of estrogen receptors in the male accessory sex organs during prepubertal life. In the present study, estrogen antagonists (CDRI-85/287 and centchroman) have been used to examine this concept by antagonising estrogen action at critical stages in the life in rat. Centchroman or 85/287 administration to 14 day old rats for 7 days did not alter gonadal or accessory organ weight. In contrast, in 21 day old castrated rats, treatment with either compound from day 28-35 of life stimulated an increase in all organ weights. When administered to normal rats during the critical phase of transition, i.e. days 30-60 of life, both testis and accessory organs showed an increase in weight. In contrast castrated rats treated with estrogen alone or in combination with 85/287 from days 37-45 of life and sacrificed on day 46 did not show any change, but 85/287 per se markedly reduced the weight of accessory organs. In adult castrated rats, the potency of DHT as a promoter of growth was potentiated by estradiol. Compound 85/287 negated the estradiol-induced increase. Glycerylphosphorylcholine (GPC) and sialic acid levels showed about 100% increase, with both high and low doses of 85/287 (treated from 30-60 days of life), However, centchroman (CDRI-67/20) was less potent in this regard. The effect of estrogen antagonists in relation to epididymal physiology during different phases of life in the rat is discussed.
最近的研究表明,雌激素对雄性生殖道有刺激作用。证据包括循环系统中可测量水平雌激素的存在、外源性雌激素的潴留,以及青春期前雄性附属生殖器官中雌激素受体的存在。在本研究中,已使用雌激素拮抗剂(CDRI-85/287和醋甲醚)通过在大鼠生命的关键阶段拮抗雌激素作用来检验这一概念。给14日龄大鼠连续7天给予醋甲醚或85/287,未改变性腺或附属器官的重量。相比之下,在21日龄去势大鼠中,从生命的第28至35天用这两种化合物中的任何一种进行治疗,都会刺激所有器官重量增加。在生命的关键转变期,即第30至60天,给正常大鼠给药时,睾丸和附属器官的重量均增加。相比之下,在生命的第37至45天单独用雌激素或与85/287联合处理并在第46天处死的去势大鼠未显示任何变化,但85/287本身显著降低了附属器官的重量。在成年去势大鼠中,雌二醇增强了双氢睾酮作为生长促进剂的效力。化合物85/287抵消了雌二醇诱导的增加。高剂量和低剂量的85/287(从生命的第30至60天开始处理)均使甘油磷酸胆碱(GPC)和唾液酸水平升高约100%,然而,在这方面醋甲醚(CDRI-67/20)的效力较低。本文讨论了雌激素拮抗剂在大鼠生命不同阶段对附睾生理学的影响。