Shinada T, Yokota Y, Igarashi M
Fertil Steril. 1978 Jan;29(1):84-7.
The inhibitory effect of various gestagens upon the pregnenolone 3 beta-ol-dehydrogenase-delta5-4-isomerase system in 10,000 X g supernatants of human corpora lutea of the menstrual cycle has been investigated in in vitro experiments. The Km value for pregnenolone was 1.3 X 10(-6) M. All gestations reduced the rate of conversion of pregnenolone to progesterone. As compared with controls, average relative rates of reaction with additives were as follows: progesterone, 47%; 17-hydroxyprogesterone, 64% norethisterone, 33%; chlormadinone acetate, 47% medroxyprogesterone acetate, 53%; dydrogesterone, 62%; and allylestrenol, 74%. The data substantiate that natural or synthetic gestagens, at least in vitro, inhibit the conversion of pregnenolone to progesterone by human corpora lutea and that natural progesterone itself is a potent inhibitor which appears to acut noncompetitively (K1 =2.2 X 10(-5) M).
在体外实验中,研究了各种孕激素对月经周期中人类黄体10,000 X g上清液中孕烯醇酮3β-醇-脱氢酶-δ5-4-异构酶系统的抑制作用。孕烯醇酮的Km值为1.3 X 10(-6) M。所有孕激素均降低了孕烯醇酮向孕酮的转化速率。与对照组相比,添加物的平均相对反应速率如下:孕酮,47%;17-羟孕酮,64%;炔诺酮,33%;醋酸氯地孕酮,47%;醋酸甲羟孕酮,53%;地屈孕酮,62%;烯丙雌醇,74%。数据证实,天然或合成孕激素至少在体外可抑制人类黄体将孕烯醇酮转化为孕酮,且天然孕酮本身就是一种强效抑制剂,似乎以非竞争性方式起作用(K1 =2.2 X 10(-5) M)。