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酮康唑及其他咪唑类杀菌剂对睾酮生物合成的影响。

Effect of ketoconazole and other imidazole fungicides on testosterone biosynthesis.

作者信息

Schürmeyer T, Nieschlag E

出版信息

Acta Endocrinol (Copenh). 1984 Feb;105(2):275-80. doi: 10.1530/acta.0.1050275.

Abstract

A single oral dose of 400 mg ketoconazole, a broad-spectrum antifungal drug, administered orally to 5 young men induced a drop in serum and saliva testosterone into the range of hypogonadism, while LH, FSH and prolactin levels remained unchanged. In vitro studies with mouse Leydig cells demonstrated a direct reversible inhibition of testosterone biosynthesis by ketoconazole. Comparative studies with chemically related compounds showed similar effects on testosterone production of mouse Leydig cells by isoconazole, miconazole, econazole and clotrimazole, while metronidazole and levamisole were without influence on testosterone biosynthesis. Since all tested imidazoles which suppress testosterone production have as a common feature a phenylated side chain of the imidazole molecule, this indicates a structure/activity relationship for the effects observed.

摘要

对5名年轻男性口服单剂量400毫克酮康唑(一种广谱抗真菌药物)后,血清和唾液睾酮水平降至性腺功能减退范围,而促黄体生成素(LH)、促卵泡生成素(FSH)和催乳素水平保持不变。对小鼠睾丸间质细胞的体外研究表明,酮康唑可直接可逆地抑制睾酮生物合成。与化学相关化合物的比较研究表明,异康唑、咪康唑、益康唑和克霉唑对小鼠睾丸间质细胞的睾酮生成有类似影响,而甲硝唑和左旋咪唑对睾酮生物合成无影响。由于所有测试的抑制睾酮生成的咪唑类药物都有一个共同特征,即咪唑分子的苯基化侧链,这表明所观察到的效应存在结构/活性关系。

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