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Manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ACE2) in heart failure

Angiotensin converting enzyme 2 (ACE2), is a monocarboxypeptidase which metabolizes several peptides including the degradation of Ang II, a peptide with vasoconstrictive/proliferative/effects, to generate Ang 1–7, which acting through its receptor Mas exerts vasodilatory/anti-proliferative actions....

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Autores principales: Patel, Vaibhav B., Putko, Brendan, Wang, Zuocheng, Zhong, Jiu-Chang, Oudit, Gavin Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185729/
https://www.ncbi.nlm.nih.gov/pubmed/32362932
http://dx.doi.org/10.1016/j.ddstr.2013.11.001
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author Patel, Vaibhav B.
Putko, Brendan
Wang, Zuocheng
Zhong, Jiu-Chang
Oudit, Gavin Y.
author_facet Patel, Vaibhav B.
Putko, Brendan
Wang, Zuocheng
Zhong, Jiu-Chang
Oudit, Gavin Y.
author_sort Patel, Vaibhav B.
collection PubMed
description Angiotensin converting enzyme 2 (ACE2), is a monocarboxypeptidase which metabolizes several peptides including the degradation of Ang II, a peptide with vasoconstrictive/proliferative/effects, to generate Ang 1–7, which acting through its receptor Mas exerts vasodilatory/anti-proliferative actions. The classical pathway of the RAS involving the ACE-Ang II-AT(1) receptor axis is antagonized by the second arm constituted by the ACE2-Ang 1–7/Mas receptor axis. Loss of ACE2 enhances the adverse pathological remodeling susceptibility to pressure-overload and myocardial infarction. Human recombinant ACE2 is also a negative regulator of Ang II-induced myocardial hypertrophy, fibrosis and diastolic dysfunction and suppresses pressure-overload induced heart failure. Due to its characteristics, the ACE2-Ang 1–7/Mas axis may represent new possibilities for developing novel therapeutic strategies for the treatment of heart failure. Human recombinant ACE2 has been safely administered to healthy human volunteers intravenously resulting in sustained lowering of plasma Ang II levels. In this review, we will summarize the beneficial effects of ACE2 in heart disease and the potential use of human recombinant ACE2 as a novel therapy for heart failure.
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spelling pubmed-71857292020-04-28 Manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ACE2) in heart failure Patel, Vaibhav B. Putko, Brendan Wang, Zuocheng Zhong, Jiu-Chang Oudit, Gavin Y. Drug Discov Today Ther Strateg Heart Failure Angiotensin converting enzyme 2 (ACE2), is a monocarboxypeptidase which metabolizes several peptides including the degradation of Ang II, a peptide with vasoconstrictive/proliferative/effects, to generate Ang 1–7, which acting through its receptor Mas exerts vasodilatory/anti-proliferative actions. The classical pathway of the RAS involving the ACE-Ang II-AT(1) receptor axis is antagonized by the second arm constituted by the ACE2-Ang 1–7/Mas receptor axis. Loss of ACE2 enhances the adverse pathological remodeling susceptibility to pressure-overload and myocardial infarction. Human recombinant ACE2 is also a negative regulator of Ang II-induced myocardial hypertrophy, fibrosis and diastolic dysfunction and suppresses pressure-overload induced heart failure. Due to its characteristics, the ACE2-Ang 1–7/Mas axis may represent new possibilities for developing novel therapeutic strategies for the treatment of heart failure. Human recombinant ACE2 has been safely administered to healthy human volunteers intravenously resulting in sustained lowering of plasma Ang II levels. In this review, we will summarize the beneficial effects of ACE2 in heart disease and the potential use of human recombinant ACE2 as a novel therapy for heart failure. Elsevier Ltd. 2012 2014-01-24 /pmc/articles/PMC7185729/ /pubmed/32362932 http://dx.doi.org/10.1016/j.ddstr.2013.11.001 Text en Copyright © 2013 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Heart Failure
Patel, Vaibhav B.
Putko, Brendan
Wang, Zuocheng
Zhong, Jiu-Chang
Oudit, Gavin Y.
Manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ACE2) in heart failure
title Manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ACE2) in heart failure
title_full Manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ACE2) in heart failure
title_fullStr Manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ACE2) in heart failure
title_full_unstemmed Manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ACE2) in heart failure
title_short Manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ACE2) in heart failure
title_sort manipulating angiotensin metabolism with angiotensin converting enzyme 2 (ace2) in heart failure
topic Heart Failure
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185729/
https://www.ncbi.nlm.nih.gov/pubmed/32362932
http://dx.doi.org/10.1016/j.ddstr.2013.11.001
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