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

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 simi...

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Autores principales: Bamberg, Krister, William-Olsson, Lena, Johansson, Ulrika, Jansson-Löfmark, Rasmus, Hartleib-Geschwindner, Judith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396052/
https://www.ncbi.nlm.nih.gov/pubmed/30813831
http://dx.doi.org/10.1177/1470320319827449
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author Bamberg, Krister
William-Olsson, Lena
Johansson, Ulrika
Jansson-Löfmark, Rasmus
Hartleib-Geschwindner, Judith
author_facet Bamberg, Krister
William-Olsson, Lena
Johansson, Ulrika
Jansson-Löfmark, Rasmus
Hartleib-Geschwindner, Judith
author_sort Bamberg, Krister
collection PubMed
description 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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spelling pubmed-63960522019-03-04 The selective mineralocorticoid receptor modulator AZD9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone Bamberg, Krister William-Olsson, Lena Johansson, Ulrika Jansson-Löfmark, Rasmus Hartleib-Geschwindner, Judith J Renin Angiotensin Aldosterone Syst Short Communication 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. SAGE Publications 2019-02-28 /pmc/articles/PMC6396052/ /pubmed/30813831 http://dx.doi.org/10.1177/1470320319827449 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Short Communication
Bamberg, Krister
William-Olsson, Lena
Johansson, Ulrika
Jansson-Löfmark, Rasmus
Hartleib-Geschwindner, Judith
The selective mineralocorticoid receptor modulator AZD9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone
title The selective mineralocorticoid receptor modulator AZD9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone
title_full The selective mineralocorticoid receptor modulator AZD9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone
title_fullStr The selective mineralocorticoid receptor modulator AZD9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone
title_full_unstemmed The selective mineralocorticoid receptor modulator AZD9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone
title_short The selective mineralocorticoid receptor modulator AZD9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone
title_sort selective mineralocorticoid receptor modulator azd9977 reveals differences in mineralocorticoid effects of aldosterone and fludrocortisone
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396052/
https://www.ncbi.nlm.nih.gov/pubmed/30813831
http://dx.doi.org/10.1177/1470320319827449
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