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氨鲁米特对正常男性睾丸类固醇生成的急性影响。

Acute effects of aminoglutethimide on testicular steroidogenesis in normal men.

作者信息

Santen R J, Cohn N, Misbin R, Samojlik E, Foltz E

出版信息

J Clin Endocrinol Metab. 1979 Oct;49(4):631-4. doi: 10.1210/jcem-49-4-631.

Abstract

Aminoglutethimide (AG), a known adrenal inhibitor, was administered acutely to normal men in order to study its effects on testicular steroidogenesis. Sixteen subjects between the ages of 21--30 yr received either placebo or 1250 mg AG in divided doses during a 24-h period. To reduce the contribution of adrenal steroids, adrenal function was inhibited in both groups of men by the administration of dexamethasone (2 mg) on the night of the experiment. As a result, mean morning plasma cortisol levels fell to less than 2 micrograms/100 ml. AG blunted the normal diurnal rise in testosterone, which was observed in men receiving placebo, and significantly suppressed the levels of this androgen at 0700 and 0900 h. Estradiol concentrations fell to a greater extent than those of testosterone. The differences between the placebo and drug treatment groups were significant at all time points except 1900 h. A pattern similar to that of estradiol was observed for plasma estrone. When the overall effect of AG administration was examined by analysis of variance, the differences in the levels of all three steroids produced by treatment were highly significant (P less than 0.01 to less than 0.001). After the inhibition of testosterone and estradiol levels, LH and FSH concentrations were significantly (P less than 0.01 and P less than 0.001, respectively) higher in men receiving AG than in those given placebo. However, the data exhibited a large variance due to pulsatile gonadotropin secretion. These observations suggested that AG induces an acute inhibition of testicular steroidogenesis and probably also of the aromatization of testosterone to estradiol.

摘要

氨鲁米特(AG)是一种已知的肾上腺抑制剂,对正常男性进行急性给药以研究其对睾丸类固醇生成的影响。16名年龄在21至30岁之间的受试者在24小时内分剂量接受了安慰剂或1250毫克AG。为了减少肾上腺类固醇的影响,在实验当晚两组男性均通过给予地塞米松(2毫克)抑制肾上腺功能。结果,早晨血浆皮质醇平均水平降至低于2微克/100毫升。AG抑制了接受安慰剂的男性中观察到的睾酮正常昼夜升高,并在0700和0900时显著抑制了这种雄激素的水平。雌二醇浓度下降的幅度大于睾酮。除1900时外,安慰剂组和药物治疗组之间的差异在所有时间点均具有显著性。血浆雌酮观察到与雌二醇相似的模式。通过方差分析检查AG给药的总体效果时,治疗产生的所有三种类固醇水平差异均具有高度显著性(P小于0.01至小于0.001)。在抑制睾酮和雌二醇水平后,接受AG的男性中LH和FSH浓度显著高于接受安慰剂的男性(分别为P小于0.01和P小于0.001)。然而,由于促性腺激素的脉冲式分泌,数据显示出较大的变异性。这些观察结果表明,AG诱导睾丸类固醇生成急性抑制,可能还抑制睾酮向雌二醇的芳香化作用。

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