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酮康唑通过抑制肾上腺11β-羟化酶来阻断人体皮质醇的分泌。

Ketoconazole blocks cortisol secretion in man by inhibition of adrenal 11 beta-hydroxylase.

作者信息

Engelhardt D, Dörr G, Jaspers C, Knorr D

出版信息

Klin Wochenschr. 1985 Jul 1;63(13):607-12. doi: 10.1007/BF01733014.

Abstract

We investigated basal and ACTH stimulated levels of cortisol, corticosterone, 17 alpha-hydroxyprogesterone, 11-deoxycortisol and 11-deoxycorticosterone as well as plasma levels of ACTH before and during the oral administration of ketoconazole in five patients with Cushing's syndrome (3 with bilateral adrenal hyperplasia, 1 with adrenal adenoma and 1 with adrenal carcinoma) and in three controls. The influence of ketoconazole on the transformation of 3H-17 alpha-hydroxyprogesterone to 3H-11-deoxycortisol and 3H-cortisol and of 3H-11-deoxycortisol to 3H-cortisol as well as of 3H-11-deoxycorticosterone to 3H-corticosterone was also examined in slices or homogenates of normal and hyperplastic adrenal tissue from four patients. Ketoconazole induced a rise of 11-deoxycortisol and 11-deoxycorticosterone, but not of cortisol and inconsistently of corticosterone which were increased by ACTH. Thus the ratio 11-deoxycortisol/cortisol rose more after ketoconazole than after ACTH and the ratio 11-deoxycorticosterone/corticosterone rose after ketoconazole but fell after ACTH. Plasma ACTH levels were stimulated 2-50 fold by ketoconazole. Incubation studies of adrenal tissue slices with 3H-17 alpha-hydroxyprogesterone showed that ketoconazole inhibited the transformation of 3H-17 alpha-hydroxyprogesterone to 3H-cortisol but not to 3H-11-deoxycortisol so that the ratio 3H-11-deoxycortisol/3H-cortisol increased 15-80 fold. After incubation of adrenal slices with 3H-11-deoxycortisol or 3H-11-deoxycorticosterone and ketoconazole, a 2-260 fold increase of the ratios 3H-11-deoxycortisol/3H-cortisol and 3H-11-deoxycorticosterone/3H-corticosterone were also found.

摘要

我们研究了5例库欣综合征患者(3例双侧肾上腺增生、1例肾上腺腺瘤和1例肾上腺皮质癌)及3例对照者在口服酮康唑之前及期间,皮质醇、皮质酮、17α-羟孕酮、11-脱氧皮质醇和11-脱氧皮质酮的基础水平及促肾上腺皮质激素(ACTH)刺激后的水平,以及血浆ACTH水平。我们还在4例患者的正常及增生肾上腺组织切片或匀浆中检测了酮康唑对3H-17α-羟孕酮向3H-11-脱氧皮质醇和3H-皮质醇转化、3H-11-脱氧皮质醇向3H-皮质醇转化以及3H-11-脱氧皮质酮向3H-皮质酮转化的影响。酮康唑导致11-脱氧皮质醇和11-脱氧皮质酮水平升高,但皮质醇水平未升高,皮质酮水平仅偶尔升高,而ACTH可使其升高。因此,酮康唑作用后11-脱氧皮质醇/皮质醇的比值升高幅度大于ACTH作用后,酮康唑作用后11-脱氧皮质酮/皮质酮的比值升高,而ACTH作用后该比值下降。酮康唑可使血浆ACTH水平升高2至50倍。用3H-17α-羟孕酮对肾上腺组织切片进行孵育研究表明,酮康唑抑制3H-17α-羟孕酮向3H-皮质醇的转化,但不抑制其向3H-11-脱氧皮质醇的转化,因此3H-11-脱氧皮质醇/3H-皮质醇的比值升高了15至80倍。用3H-11-脱氧皮质醇或3H-11-脱氧皮质酮与酮康唑对肾上腺切片进行孵育后,还发现3H-11-脱氧皮质醇/3H-皮质醇和3H-11-脱氧皮质酮/3H-皮质酮的比值分别升高了2至260倍。

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