睾酮在体外抑制人野生型和嵌合型醛固酮合成酶活性

C. Fardella, A. Vecchiola, Cristóbal A. Fuentes, Isidora Solar, C. Campino, C. Carvajal, C. Lagos
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引用次数: 0

摘要

我们最近报道了在体外,野生型(ASWT)和嵌合醛固酮合成酶(ASCE)酶被黄体酮抑制,而雌二醇没有作用。为了探索睾酮对野生型和嵌合型醛固酮合成酶的直接作用,我们使用含有ASWT或ASWT完整cdna的载体瞬时转染HEK-293细胞进行了体外实验。在有或没有增加睾酮剂量的情况下,用脱氧皮质酮(DOC)培养,评估睾酮对AS酶活性的影响。采用HPLC-MS/MS法测定醛固酮产量。在两种酶的活性位点内进行睾酮对接。在该系统中,睾酮抑制ASWT (5 μM抑制90%,IC50=1.690 μM)的效果和效力高于ASCE (5 μM抑制80%,IC50=3.176 μM)。我们的研究结果显示睾酮对ASWT或ASCE酶合成醛固酮有抑制作用。该效应是睾酮作用的一种新的调控机制,可能影响原发性醛固酮增多症的筛查和诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Testosterone inhibits Human Wild-Type and Chimeric Aldosterone Synthase Activity In-vitro
We have recently reported that in vitro, the wild-type (ASWT) and chimeric aldosterone synthase (ASCE) enzymes are inhibited by progesterone and estradiol had no effect. To explore the direct action of testosterone on wild-type and chimeric aldosterone synthase enzymes, we carried out an in vitro assay using HEK-293 cells transiently transfected with vectors containing the full ASWT or ASWT cDNAs. The effect of testosterone on AS enzyme activities was evaluated incubating with deoxycorticosterone (DOC) with or without increasing doses of testosterone. Aldosterone production was measured by HPLC-MS/MS. Docking of testosterone within the active sites of both enzymes was performed. In this system, testosterone inhibited ASWT, (90% inhibition at 5 μM, IC50=1.690 μM) with higher efficacy and potency than the ASCE (80% inhibition at 5 μM, IC50=3.176 μM). Our results show an inhibitory effect of testosterone on aldosteronesynthesis by ASWT or ASCE enzyme. This effect is a novel regulatory mechanism of testosterone action, which could affect the screening and diagnosis of primary aldosteronism.
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