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曲洛司坦与正常下丘脑-垂体-睾丸轴

Trilostane and the normal hypothalamic-pituitary-testicular axis.

作者信息

Semple C G, Weir S W, Thomson J A, Beastall G H

出版信息

Clin Endocrinol (Oxf). 1982 Jul 1;17(1):99-102. doi: 10.1111/j.1365-2265.1982.tb02639.x.

Abstract

Trilostane, a competitive inhibitor of the 3 beta-hydroxysteroid dehydrogenase enzyme system, has adrenal blocking activity and has been used to treat Cushing's syndrome and other disease. To investigate is effect on the normal human hypothalamic-pituitary-testicular axis, trilostane (initially 240 mg/day) was given to ten healthy adult males, the dose increasing at weekly intervals by 240 mg/day up to 960 mg/day. When chromatography was used to remove trilostane and metabolites from the assay system, serum testosterone was found to fall on trilostane therapy (P less than 0.01) and this was accompanied by a rise in LH (P less than 0.01). The responses of FSH and LH to LHRH were unaffected by treatment. It is concluded that trilostane inhibits human testicular 3 beta-hydroxysteroid dehydrogenase and male patients on trilostane should be monitored for sexual dysfunction and impairment of testicular steroidogenesis.

摘要

曲洛司坦是3β-羟基类固醇脱氢酶系统的竞争性抑制剂,具有肾上腺阻断活性,已被用于治疗库欣综合征和其他疾病。为研究其对正常人类下丘脑-垂体-睾丸轴的影响,对10名健康成年男性给予曲洛司坦(初始剂量为240毫克/天),剂量每周增加240毫克/天,直至960毫克/天。当使用色谱法从检测系统中去除曲洛司坦及其代谢产物时,发现血清睾酮在曲洛司坦治疗时下降(P<0.01),同时LH升高(P<0.01)。FSH和LH对LHRH的反应不受治疗影响。结论是曲洛司坦抑制人类睾丸3β-羟基类固醇脱氢酶,接受曲洛司坦治疗的男性患者应监测性功能障碍和睾丸类固醇生成受损情况。

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