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ACE2 and COVID-19 and the resulting ARDS
This article reviews the correlation between ACE2 and COVID-19 and the resulting acute respiratory distress syndrome (ARDS). ACE2 is a crucial component of the renin-angiotensin system (RAS). The classical ACE-angiotensin Ⅱ (Ang II)-angiotensin type 1 receptor (AT1R) axis and the ACE2-Ang(1-7)-Mas c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016912/ https://www.ncbi.nlm.nih.gov/pubmed/32522846 http://dx.doi.org/10.1136/postgradmedj-2020-137935 |
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author | Zhang, Xiaoqing Li, Shuren Niu, Shaoqian |
author_facet | Zhang, Xiaoqing Li, Shuren Niu, Shaoqian |
author_sort | Zhang, Xiaoqing |
collection | PubMed |
description | This article reviews the correlation between ACE2 and COVID-19 and the resulting acute respiratory distress syndrome (ARDS). ACE2 is a crucial component of the renin-angiotensin system (RAS). The classical ACE-angiotensin Ⅱ (Ang II)-angiotensin type 1 receptor (AT1R) axis and the ACE2-Ang(1-7)-Mas counter-regulatory axis play an essential role in RAS system. ACE2 antagonises the activation of the classical RAS ACE-Ang II-AT1R axis and protects against lung injury. Similar to severe acute respiratory syndrome-related coronavirus, 2019 novel coronavirus (2019-nCoV) also uses ACE2 for cell entry. ARDS is a clinical high-mortality disease which is probably due to the excessive activation of RAS caused by 2019-nCoV infection, and ACE2 has a protective effect on ARDS caused by COVID-19. Because of these protective effects of ACE2 on ARDS, the development of drugs enhancing ACE2 activity may become one of the most promising approaches for the treatment of COVID-19 in the near future. In the meantime, however, the use of RAS blockers such as ACE inhibitors and angiotensin II receptor blockers that inhibit the damaging (ACE-Ang II) arm of the RAS cascade in the lung may also be promising. Trial registration number: NCT04287686. |
format | Online Article Text |
id | pubmed-10016912 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100169122023-05-23 ACE2 and COVID-19 and the resulting ARDS Zhang, Xiaoqing Li, Shuren Niu, Shaoqian Postgrad Med J Review This article reviews the correlation between ACE2 and COVID-19 and the resulting acute respiratory distress syndrome (ARDS). ACE2 is a crucial component of the renin-angiotensin system (RAS). The classical ACE-angiotensin Ⅱ (Ang II)-angiotensin type 1 receptor (AT1R) axis and the ACE2-Ang(1-7)-Mas counter-regulatory axis play an essential role in RAS system. ACE2 antagonises the activation of the classical RAS ACE-Ang II-AT1R axis and protects against lung injury. Similar to severe acute respiratory syndrome-related coronavirus, 2019 novel coronavirus (2019-nCoV) also uses ACE2 for cell entry. ARDS is a clinical high-mortality disease which is probably due to the excessive activation of RAS caused by 2019-nCoV infection, and ACE2 has a protective effect on ARDS caused by COVID-19. Because of these protective effects of ACE2 on ARDS, the development of drugs enhancing ACE2 activity may become one of the most promising approaches for the treatment of COVID-19 in the near future. In the meantime, however, the use of RAS blockers such as ACE inhibitors and angiotensin II receptor blockers that inhibit the damaging (ACE-Ang II) arm of the RAS cascade in the lung may also be promising. Trial registration number: NCT04287686. Oxford University Press 2020-06-10 /pmc/articles/PMC10016912/ /pubmed/32522846 http://dx.doi.org/10.1136/postgradmedj-2020-137935 Text en © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Review Zhang, Xiaoqing Li, Shuren Niu, Shaoqian ACE2 and COVID-19 and the resulting ARDS |
title | ACE2 and COVID-19 and the resulting ARDS |
title_full | ACE2 and COVID-19 and the resulting ARDS |
title_fullStr | ACE2 and COVID-19 and the resulting ARDS |
title_full_unstemmed | ACE2 and COVID-19 and the resulting ARDS |
title_short | ACE2 and COVID-19 and the resulting ARDS |
title_sort | ace2 and covid-19 and the resulting ards |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016912/ https://www.ncbi.nlm.nih.gov/pubmed/32522846 http://dx.doi.org/10.1136/postgradmedj-2020-137935 |
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