New Cardiovascular and Pulmonary Therapeutic Strategies Based on the Angiotensin-Converting Enzyme 2/Angiotensin-(1–7)/Mas Receptor Axis

Angiotensin (Ang)-(1–7) is now recognized as a biologically active component of the renin-angiotensin system (RAS). The discovery of the angiotensin-converting enzyme homologue ACE2 revealed important metabolic pathways involved in the Ang-(1–7) synthesis. This enzyme can form Ang-(1–7) from Ang II...

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Main Authors: Anderson J. Ferreira, Tatiane M. Murça, Rodrigo A. Fraga-Silva, Carlos Henrique Castro, Mohan K. Raizada, Robson A. S. Santos
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:International Journal of Hypertension
Online Access:http://dx.doi.org/10.1155/2012/147825
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author Anderson J. Ferreira
Tatiane M. Murça
Rodrigo A. Fraga-Silva
Carlos Henrique Castro
Mohan K. Raizada
Robson A. S. Santos
author_facet Anderson J. Ferreira
Tatiane M. Murça
Rodrigo A. Fraga-Silva
Carlos Henrique Castro
Mohan K. Raizada
Robson A. S. Santos
author_sort Anderson J. Ferreira
collection DOAJ
description Angiotensin (Ang)-(1–7) is now recognized as a biologically active component of the renin-angiotensin system (RAS). The discovery of the angiotensin-converting enzyme homologue ACE2 revealed important metabolic pathways involved in the Ang-(1–7) synthesis. This enzyme can form Ang-(1–7) from Ang II or less efficiently through hydrolysis of Ang I to Ang-(1–9) with subsequent Ang-(1–7) formation. Additionally, it is well established that the G protein-coupled receptor Mas is a functional ligand site for Ang-(1–7). The axis formed by ACE2/Ang-(1–7)/Mas represents an endogenous counter regulatory pathway within the RAS whose actions are opposite to the vasoconstrictor/proliferative arm of the RAS constituted by ACE/Ang II/AT1 receptor. In this review we will discuss recent findings concerning the biological role of the ACE2/Ang-(1–7)/Mas arm in the cardiovascular and pulmonary system. Also, we will highlight the initiatives to develop potential therapeutic strategies based on this axis.
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issn 2090-0384
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publishDate 2012-01-01
publisher Wiley
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series International Journal of Hypertension
spelling doaj-art-f513b43cb05f4b57ba69243db59772802025-02-03T01:12:07ZengWileyInternational Journal of Hypertension2090-03842090-03922012-01-01201210.1155/2012/147825147825New Cardiovascular and Pulmonary Therapeutic Strategies Based on the Angiotensin-Converting Enzyme 2/Angiotensin-(1–7)/Mas Receptor AxisAnderson J. Ferreira0Tatiane M. Murça1Rodrigo A. Fraga-Silva2Carlos Henrique Castro3Mohan K. Raizada4Robson A. S. Santos5Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, BrazilDepartment of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, BrazilDepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, BrazilDepartment of Physiology Sciences, Federal University of Goiás, 74.001-970 Goiânia, GO, BrazilDepartment of Physiology and Functional Genomics, College of Medicine, University of Florida, 32.610 Gainesville, FL, USADepartment of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais, 31.270-901 Belo Horizonte, MG, BrazilAngiotensin (Ang)-(1–7) is now recognized as a biologically active component of the renin-angiotensin system (RAS). The discovery of the angiotensin-converting enzyme homologue ACE2 revealed important metabolic pathways involved in the Ang-(1–7) synthesis. This enzyme can form Ang-(1–7) from Ang II or less efficiently through hydrolysis of Ang I to Ang-(1–9) with subsequent Ang-(1–7) formation. Additionally, it is well established that the G protein-coupled receptor Mas is a functional ligand site for Ang-(1–7). The axis formed by ACE2/Ang-(1–7)/Mas represents an endogenous counter regulatory pathway within the RAS whose actions are opposite to the vasoconstrictor/proliferative arm of the RAS constituted by ACE/Ang II/AT1 receptor. In this review we will discuss recent findings concerning the biological role of the ACE2/Ang-(1–7)/Mas arm in the cardiovascular and pulmonary system. Also, we will highlight the initiatives to develop potential therapeutic strategies based on this axis.http://dx.doi.org/10.1155/2012/147825
spellingShingle Anderson J. Ferreira
Tatiane M. Murça
Rodrigo A. Fraga-Silva
Carlos Henrique Castro
Mohan K. Raizada
Robson A. S. Santos
New Cardiovascular and Pulmonary Therapeutic Strategies Based on the Angiotensin-Converting Enzyme 2/Angiotensin-(1–7)/Mas Receptor Axis
International Journal of Hypertension
title New Cardiovascular and Pulmonary Therapeutic Strategies Based on the Angiotensin-Converting Enzyme 2/Angiotensin-(1–7)/Mas Receptor Axis
title_full New Cardiovascular and Pulmonary Therapeutic Strategies Based on the Angiotensin-Converting Enzyme 2/Angiotensin-(1–7)/Mas Receptor Axis
title_fullStr New Cardiovascular and Pulmonary Therapeutic Strategies Based on the Angiotensin-Converting Enzyme 2/Angiotensin-(1–7)/Mas Receptor Axis
title_full_unstemmed New Cardiovascular and Pulmonary Therapeutic Strategies Based on the Angiotensin-Converting Enzyme 2/Angiotensin-(1–7)/Mas Receptor Axis
title_short New Cardiovascular and Pulmonary Therapeutic Strategies Based on the Angiotensin-Converting Enzyme 2/Angiotensin-(1–7)/Mas Receptor Axis
title_sort new cardiovascular and pulmonary therapeutic strategies based on the angiotensin converting enzyme 2 angiotensin 1 7 mas receptor axis
url http://dx.doi.org/10.1155/2012/147825
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