The selective mineralocorticoid receptor modulator AZD9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone

被引:16
作者
Bamberg, Krister [1 ]
William-Olsson, Lena [1 ]
Johansson, Ulrika [1 ]
Jansson-Lofmark, Rasmus [2 ]
Hartleib-Geschwindner, Judith [1 ]
机构
[1] AstraZeneca, IMED Biotech Unit, Cardiovasc Renal & Metab, Biosci CKD, Molndal, Sweden
[2] AstraZeneca, IMED Biotech Unit, Cardiovasc Renal & Metab, Drug Metab & Pharmacokinet, Molndal, Sweden
关键词
Aldosterone; AZD9977; fludrocortisone; mineralocorticoid receptor ligand; urinary electrolytes; ANTAGONISTS; ACTIVATION; ASSAY;
D O I
10.1177/1470320319827449
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Introduction: AZD9977 is a novel mineralocorticoid receptor (MR) modulator, which in preclinical studies demonstrated organ protection without affecting aldosterone-regulated urinary electrolyte excretion. However, when tested in humans, using fludrocortisone as an MR agonist, AZD9977 exhibited similar effects on urinary Na+/K+ ratio as eplerenone. The aim of this study is to understand whether the contradictory results seen in rats and humans are due to the mineralocorticoid used. Materials and methods: Rats were treated with single doses of AZD9977 or eplerenone in combination with either aldosterone or fludrocortisone. Urine was collected for five to six hours and total amounts excreted Na+ and K+ were assessed. Results: AZD9977 dose-dependently increased urinary Na+/K+ ratio in rats when tested against fludrocortisone, but not when tested against aldosterone. Eplerenone dose-dependently increased urinary Na+/K+ ratio when tested against fludrocortisone as well as aldosterone. Conclusions: The data suggest that the contrasting effects of AZD9977 on urinary electrolyte excretion observed in rats and humans are due to the use of the synthetic mineralocorticoid fludrocortisone. Future clinical studies are required to confirm the reduced electrolyte effects of AZD9977 and the subsequent lower predicted hyperkalemia risk.
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页数:6
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