Barnea E R, Maheux R, Caldwell B V, DeFazio J, DeCherney A H, Naftolin F
J Endocrinol Invest. 1985 Aug;8(4):297-302. doi: 10.1007/BF03348501.
A dose response curve for LRFD6a-a potent LRF agonist-was established in normal midluteal phase women. At low doses (3-10 micrograms) an acute stimulatory effect on gonadotropins and ovarian steroidogenesis of estradiol and progesterone was observed. Despite large increases in circulating gonadotropins following the highest dose (30 micrograms LRFD6a), no acute changes in plasma steroids were noted. A sharp drop in progesterone was present after 3 days, with significant shortening of the cycle in 3 of 4 subjects in the group. While the stimulatory effect may be due to gonadotropin release and local action, the luteolytic effect observed is suggested to be a consequence of the direct inhibitory effect of the analog on ovarian function.
在正常黄体中期的女性中建立了LRFD6a(一种强效促黄体生成素释放因子激动剂)的剂量反应曲线。在低剂量(3 - 10微克)时,观察到对促性腺激素以及雌二醇和孕酮的卵巢甾体生成有急性刺激作用。尽管在最高剂量(30微克LRFD6a)后循环促性腺激素大幅增加,但未观察到血浆类固醇有急性变化。3天后孕酮急剧下降,该组4名受试者中有3名的月经周期显著缩短。虽然刺激作用可能是由于促性腺激素释放和局部作用,但观察到的黄体溶解作用被认为是该类似物对卵巢功能直接抑制作用的结果。