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Ouabain is a potent inhibitor of aldosterone secretion and angiotensin action in the human adrenal.

作者信息

Antonipillai I, Schick K, Horton R

机构信息

Department of Medicine, University of Southern California School of Medicine, Los Angeles 90033, USA.

出版信息

J Clin Endocrinol Metab. 1996 Jun;81(6):2335-7. doi: 10.1210/jcem.81.6.8964873.

DOI:10.1210/jcem.81.6.8964873
PMID:8964873
Abstract

Digitalis glycosides and a putative ouabain-like substance act by inhibiting Na,K-adenosine triphosphatases and could regulate aldosterone secretion. We studied the effects of ouabain on basal and angiotensin II (AII)-induced aldosterone in rat and human adrenal glomerulosa cells. In the rat, ouabain at doses as high as 10(-4) mol/L had no effect on basal aldosterone secretion, but caused a dose-related inhibition of AII and ACTH secretion. In human glomerulosa cells, ouabain was 1000 times more potent on both basal and AII stimulation, with action at 10(-8) mol/L. The effect of ACTH was also blunted by 10(-8)-10(-7) mol/L ouabain. However, the effect of potassium (8.7 mmol/L) on aldosterone was not altered by these doses of ouabain. These results suggest that nanomolar levels of ouabain can reduce aldosterone secretion from human zona glomerulosa cells.

摘要

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引用本文的文献

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Minireview: potassium channels and aldosterone dysregulation: is primary aldosteronism a potassium channelopathy?综述:钾离子通道与醛固酮失调:原发性醛固酮增多症是否为钾离子通道病?
Endocrinology. 2014 Jan;155(1):47-55. doi: 10.1210/en.2013-1733. Epub 2013 Dec 20.