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Novel RAAS agonists and antagonists: clinical applications and controversies
The renin–angiotensin–aldosterone system (RAAS) regulates blood pressure homeostasis and vascular injury and repair responses. The RAAS was originally thought to be an endocrine system critically important in regulating blood pressure homeostasis. Yet, important local forms of the RAAS have been des...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7097622/ https://www.ncbi.nlm.nih.gov/pubmed/25666495 http://dx.doi.org/10.1038/nrendo.2015.6 |
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author | Romero, Cesar A. Orias, Marcelo Weir, Matthew R. |
author_facet | Romero, Cesar A. Orias, Marcelo Weir, Matthew R. |
author_sort | Romero, Cesar A. |
collection | PubMed |
description | The renin–angiotensin–aldosterone system (RAAS) regulates blood pressure homeostasis and vascular injury and repair responses. The RAAS was originally thought to be an endocrine system critically important in regulating blood pressure homeostasis. Yet, important local forms of the RAAS have been described in many tissues, which are mostly independent of the systemic RAAS. These systems have been associated with diverse physiological functions, but also with inflammation, fibrosis and target-organ damage. Pharmacological modulation of the RAAS has brought about important advances in preventing morbidity and mortality associated with cardiovascular disease. Yet, traditional RAAS blockers such as angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs) only reduce the risk of disease progression in patients with established cardiovascular or renal disease by ∼20% compared with other therapies. As more components of the RAAS are described, other potential therapeutic targets emerge, which could provide improved cardiovascular and renal protection beyond that provided by an ACE inhibitor or ARB. This Review summarizes the present and future pharmacological manipulation of this important system. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nrendo.2015.6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7097622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70976222020-03-26 Novel RAAS agonists and antagonists: clinical applications and controversies Romero, Cesar A. Orias, Marcelo Weir, Matthew R. Nat Rev Endocrinol Article The renin–angiotensin–aldosterone system (RAAS) regulates blood pressure homeostasis and vascular injury and repair responses. The RAAS was originally thought to be an endocrine system critically important in regulating blood pressure homeostasis. Yet, important local forms of the RAAS have been described in many tissues, which are mostly independent of the systemic RAAS. These systems have been associated with diverse physiological functions, but also with inflammation, fibrosis and target-organ damage. Pharmacological modulation of the RAAS has brought about important advances in preventing morbidity and mortality associated with cardiovascular disease. Yet, traditional RAAS blockers such as angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs) only reduce the risk of disease progression in patients with established cardiovascular or renal disease by ∼20% compared with other therapies. As more components of the RAAS are described, other potential therapeutic targets emerge, which could provide improved cardiovascular and renal protection beyond that provided by an ACE inhibitor or ARB. This Review summarizes the present and future pharmacological manipulation of this important system. SUPPLEMENTARY INFORMATION: The online version of this article (doi:10.1038/nrendo.2015.6) contains supplementary material, which is available to authorized users. Nature Publishing Group UK 2015-02-10 2015 /pmc/articles/PMC7097622/ /pubmed/25666495 http://dx.doi.org/10.1038/nrendo.2015.6 Text en © Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 2015 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Romero, Cesar A. Orias, Marcelo Weir, Matthew R. Novel RAAS agonists and antagonists: clinical applications and controversies |
title | Novel RAAS agonists and antagonists: clinical applications and controversies |
title_full | Novel RAAS agonists and antagonists: clinical applications and controversies |
title_fullStr | Novel RAAS agonists and antagonists: clinical applications and controversies |
title_full_unstemmed | Novel RAAS agonists and antagonists: clinical applications and controversies |
title_short | Novel RAAS agonists and antagonists: clinical applications and controversies |
title_sort | novel raas agonists and antagonists: clinical applications and controversies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7097622/ https://www.ncbi.nlm.nih.gov/pubmed/25666495 http://dx.doi.org/10.1038/nrendo.2015.6 |
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