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庚酸雌二醇雌激素活性的实验研究结果。

Experimental findings on the estrogenic activity of estradiol enantate.

作者信息

Wiemeyer J C, Guerreiro R B, Fernandez M, Sagasta C L

出版信息

Arzneimittelforschung. 1986 Nov;36(11):1667-70.

PMID:3814224
Abstract

In a first attempt to find out the estrogenic activity of the monthly injectable contraceptive composed of dihydroxyprogesterone acetophenide 150 mg + estradiol enantate 10 mg (Perlutal, Topasel), estradiol enantate (estra-1,3,5(10)-triene-3-ol-17 beta-heptanoat), estradiol benzoate and ethinylestradiol were compared in rats of the Chbb: THOM species. Estradiol benzoate potency was significantly higher than that of estradiol enantate: 20.34 (15.57-26.31) times in the vaginal cornification test in castrated females; 2.21 (1.63-2.98) times in the uterine weight test also in castrated rats and 2.91 (1.86-4.54) times in the vaginal opening test in immature rats. Ethinylestradiol, orally administered in the first two tests, was less active than the other two parenterally given substances; it overcame them in the vaginal opening test, when all substances were perivaginally administered. The duration of action of equivalent doses on the vaginal smear in castrated females resulted higher for estradiol enantate: 2.52 times more than estradiol benzoate and 5.2 times more than ethinylestradiol. Based on these results and on preexistent literature, the estradiol enantate dosis which would be sufficient to obtain the endometrial proliferation in women was extrapolated and compared with those already established of estradiol benzoate and ethinylestradiol. Finally, the possibility that the estrogenic potency of the injectable contraceptive treatment can be similar or lower than the oral one with pills containing ethinylestradiol 0.030-0.050 mg is discussed.

摘要

为了首次探究由150毫克醋炔诺酮+10毫克戊酸雌二醇组成的每月注射用避孕药(Perlutal,Topasel)的雌激素活性,在Chbb:THOM品系大鼠中比较了戊酸雌二醇(estra-1,3,5(10)-三烯-3-醇-17β-庚酸酯)、苯甲酸雌二醇和炔雌醇。苯甲酸雌二醇的效力显著高于戊酸雌二醇:在去势雌性大鼠的阴道角化试验中高20.34(15.57 - 26.31)倍;在去势大鼠的子宫重量试验中高2.21(1.63 - 2.98)倍;在未成熟大鼠的阴道开口试验中高2.91(1.86 - 4.54)倍。在前两项试验中口服的炔雌醇,其活性低于另外两种经肠胃外给药的物质;当所有物质经阴道周围给药时,在阴道开口试验中它超过了这两种物质。等效剂量对去势雌性大鼠阴道涂片的作用持续时间,戊酸雌二醇更长:比苯甲酸雌二醇多2.52倍,比炔雌醇多5.2倍。基于这些结果和已有文献,推算出足以使女性子宫内膜增殖的戊酸雌二醇剂量,并与已确定的苯甲酸雌二醇和炔雌醇剂量进行比较。最后,讨论了注射用避孕药治疗的雌激素效力可能与含0.030 - 0.050毫克炔雌醇的口服避孕药相似或更低的可能性。

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