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

被引:16
作者
Antonipillai, I [1 ]
Schick, K [1 ]
Horton, R [1 ]
机构
[1] UNIV SO CALIF, SCH MED,DEPT MED,DIV ENDOCRINOL DIABET HYPERTENS, LOS ANGELES, CA 90033 USA
关键词
D O I
10.1210/jc.81.6.2335
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
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页码:2335 / 2337
页数:3
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