Fern M, Rose D P, Fern E B
Obstet Gynecol. 1978 May;51(5):541-4. doi: 10.1097/00006250-197805000-00005.
Plasma dehydroepiandrosterone (DHEA), its sulfate ester (DHEAS), and androstenedione (A2), delta5-pregnenolone (delta5-P), and 17 alpha-hydroxypregnenolone were measured in women using estrogen-containing oral contraceptives and in female controls of similar age. All three androgenic steroids and their two C21 precursors were reduced in the oral contraceptive users compared with the controls. It is concluded that oral contraceptives cause a decrease in plasma DHEA, DHEAS, and A2, one possible mechanism for which is the inhibition of delta5-P synthesis from cholesterol.
对使用含雌激素口服避孕药的女性及其年龄相仿的女性对照者,测定了血浆脱氢表雄酮(DHEA)、其硫酸酯(DHEAS)、雄烯二酮(A2)、δ5-孕烯醇酮(δ5-P)和17α-羟孕烯醇酮。与对照者相比,口服避孕药使用者的所有三种雄激素类固醇及其两种C21前体均降低。得出的结论是,口服避孕药会导致血浆DHEA、DHEAS和A2降低,其一种可能机制是抑制胆固醇合成δ5-P。