De Coster R, Caers I, Haelterman C, Debroye M
Eur J Clin Pharmacol. 1985;29(4):489-93. doi: 10.1007/BF00613467.
The effect of a single oral dose of 400 mg ketoconazole, given as an 80 mg/ml suspension, on total and physiologically free (i.e. non-sex hormone-bound) testosterone and 17 beta-oestradiol has been investigated in 6 healthy male volunteers. The two steroids fell to nadir levels of 18 and 60% of their respective initial concentrations 6 hours after drug intake, and then completely recovered. Although in vitro slight displacement of testosterone from the sex-hormone binding globulin, by high doses of ketoconazole was found, the physiologically free concentration of testosterone in vivo was closely correlated with that of the total hormone, suggesting that there is no direct interference with sex-hormone binding globulin in vivo. Plasma LH and FSH were not significantly modified by treatment. The effect of ketoconazole on plasma oestradiol levels was less pronounced and was not clearly related to a block of the aromatase system, as reported in vitro.
以80mg/ml悬浮液形式口服400mg酮康唑单剂量对6名健康男性志愿者的总睾酮、生理游离睾酮(即非性激素结合睾酮)和17β-雌二醇的影响已得到研究。服药6小时后,这两种甾体激素降至各自初始浓度的最低点,分别为18%和60%,随后完全恢复。尽管在体外发现高剂量酮康唑可使睾酮从性激素结合球蛋白上稍有解离,但体内睾酮的生理游离浓度与总激素浓度密切相关,这表明酮康唑在体内对性激素结合球蛋白没有直接干扰。治疗后血浆促黄体生成素(LH)和促卵泡生成素(FSH)无明显改变。酮康唑对血浆雌二醇水平的影响较小,且与体外报道的对芳香化酶系统的阻断无明显关系。