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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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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. |
format | Online Article Text |
id | pubmed-6396052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
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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