螺内酯治疗对妊娠期肾素-醛固酮系统的影响。

R Lammintausta, R Erkkola
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引用次数: 0

摘要

10例孕妇服用螺内酯(100mg / d)治疗2周。对妊娠水肿患者进行持续长期的钠治疗。此外,补充钾(30 mmol/天),直到螺内酯治疗开始。接受治疗的患者尿醛固酮平均排泄量(dU-Aldo)比未怀孕的患者高10倍以上。卡侬酮是螺内酯在血浆中的有效转化产物,与未怀孕的受试者一样,在3天内达到稳定水平。服用螺内酯两周内dU-Aldo下降36% (p < 0.05)。因此,低临床剂量的螺内酯对醛固酮分泌的抑制也很明显。尿钾排泄量(dU-K)在第1天下降(p < 0.05),并在螺内酯治疗1周内继续下降21% (p < 0.001)。dU-K的下降反映了在研究开始时停止补充钾。尿钠排泄未见变化。血浆肾素活性(PRA)在一周内升高79%,PRA与dU-Aldo呈负相关(p < 0.001)。在我们的研究中,钠尿不能解释PRA的增加。我们的研究显示了醛固酮的另一种反馈效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of spironolactone treatment on the renin-aldosterone system during pregnancy.

Ten pregnant patients were treated with spironolactone (100 mg daily) for two weeks. The patients were on a continuous long-term saluretic therapy for pregnancy edema. In addition, a potassium supplementation (30 mmol/day) was given until the beginning of spironolactone treatment. The patients thus treated had a mean urinary aldosterone excretion (dU-Aldo) of more than ten-fold in comparison to that of non pregnant state. Canrenone, the effective conversion product of spironolactone in plasma, reached its steady state level in three days as in non-pregnant subjects. dU-Aldo decreased in two weeks during the spironolactone by 36% (p less than 0.05). The inhibition of aldosterone secretion is thus evident also after a low clinical dose of spironolactone. Urinary potassium excretion (dU-K) decreased during the 1st day (p less than 0.05) and continued to decrease during one week of spironolactone therapy by a total of 21% (p less than 0.001). The decrease in dU-K reflects the cessation of potassium supplements in the beginning of the study. No changes in urinary sodium excretion were found. Plasma renin activity (PRA) increased in one week by 79 per cent and the changes of PRA and dU-Aldo showed inverse correlation (p less than 0.001). In our study natriuresis, cannot explain the increase of PRA. Our study suggests another feedback effect of aldosterone.

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