Clark J H, Guthrie S C
J Steroid Biochem. 1983 May;18(5):513-7. doi: 10.1016/0022-4731(83)90124-3.
The ability of clomiphene and its isomers to cause estrogenic responses during the neonatal period in the rat was examined. Rats were injected s.c. with clomiphene (CL), zuclomiphene (ZUC) or enclomiphene (ENC) on days 1,3, and 5 of life and the stimulation of the reproductive tract and estrogen receptor binding was observed. Uterine weight and DNA content were increased significantly by day 7 in animals treated with clomiphene or zuclomiphene. Uterine epithelial hypertrophy was present in all groups by day 10 and hyperplasia was present in the animals treated with ZUC and CL. The time of vaginal opening was greatly accelerated in all drug treated groups with the earliest day of opening occurring on day 7. Ovarian hemorrhage and blood in the periovarian sac occurred between days 12-14 and continued to be present through day 25. Drug treatment caused the estrogen receptor to accumulate in the nuclear fraction of the uterus and to be depleted from the cytosol fraction. We conclude that clomiphene administered to neonatal rats causes estrogenic stimulation of the reproductive tract in a fashion similar to other estrogens. This stimulation may account for the reproductive tract abnormalities which develop in rats treated with those drugs during the neonatal period.
研究了克罗米芬及其异构体在新生大鼠新生儿期引起雌激素反应的能力。在出生后第1、3和5天给大鼠皮下注射克罗米芬(CL)、组氨瑞林(ZUC)或恩氯米芬(ENC),并观察生殖道的刺激情况和雌激素受体结合情况。到第7天时,用克罗米芬或组氨瑞林处理的动物子宫重量和DNA含量显著增加。到第10天时,所有组均出现子宫上皮肥大,用ZUC和CL处理的动物出现增生。所有药物处理组阴道开口时间均大大提前,最早在第7天开口。卵巢出血和卵巢周围囊内积血发生在第12 - 14天,并持续到第25天。药物处理导致雌激素受体在子宫的核部分积累,并从胞质部分耗尽。我们得出结论,给新生大鼠施用克罗米芬会以类似于其他雌激素的方式引起生殖道的雌激素刺激。这种刺激可能是新生期用这些药物处理的大鼠出现生殖道异常的原因。