正常人19-羟基雄烯二酮的分泌调节。

H Morita, T Mune, K Yasuda, L B Mercado-Asis, M Murayama, N Yamakita, S Miyazaki, K Miura
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引用次数: 6

摘要

为评价19-羟基雄烯二酮(19-OH-AD)的分泌调节作用,测定50例正常人acth -肾上腺轴及肾素-血管紧张素系统刺激抑制试验前后的血药浓度。血浆19-OH-AD基础水平与血浆肾素活性(PRA)和血浆醛固酮浓度(PAC)均无相关性,但与血浆皮质醇水平呈正相关。0.25 mg ACTH-(1-24)刺激血浆19-OH-AD, 1 mg地塞米松(DEX)抑制血浆皮质醇和PAC。另一方面,单独静置2小时或静脉注射40 mg速尿加静置2小时,血浆19-OH-AD和皮质醇未升高,但PRA和PAC升高。静脉滴注呋塞米加3 mg去氧苄啶预处理2小时,血浆19-OH-AD和皮质醇也无反应,但PRA和PAC升高。口服卡托普利25 mg,吡格酮3 mg预处理1 h,血浆19-OH-AD和皮质醇无变化,但PAC降低。这些结果表明19-OH-AD的分泌主要受acth -肾上腺轴而非肾素-血管紧张素系统的控制。
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Secretory regulation of 19-hydroxyandrostenedione in normal man.

To evaluate the secretory regulation of 19-hydroxyandrostenedione (19-OH-AD), its plasma concentration was measured before and after stimulation and inhibition tests for the ACTH-adrenal axis and the renin-angiotensin system in 50 normal subjects. Basal levels of plasma 19-OH-AD did not correlate with either those of plasma renin activity (PRA) or the plasma aldosterone concentration (PAC), but positively correlated with those of plasma cortisol. Plasma 19-OH-AD was stimulated by 0.25 mg ACTH-(1-24) and was suppressed by 1 mg dexamethasone (DEX) as were plasma cortisol and PAC. On the other hand, with 2-h standing alone or iv 40 mg furosemide plus 2-h standing, plasma 19-OH-AD and cortisol did not increase but PRA and PAC did. With iv furosemide plus 2-h standing with 3 mg DEX pretreatment, plasma 19-OH-AD and cortisol did not respond either, but PRA and PAC increased. With 25 mg oral captopril following 1-h standing with 3 mg DEX pretreatment, plasma 19-OH-AD and cortisol did not change but PAC decreased. These results indicate that the secretion of 19-OH-AD is mainly under the control of the ACTH-adrenal axis rather than the renin-angiotensin system.

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