Countermeasure and therapeutic: A(1–7) to treat acute respiratory distress syndrome due to COVID-19 infection

In the wake of the COVID-19 pandemic it has become clear that there is a need for therapies that are capable of reducing damage caused to patients from infections. Infections that induce Acute Respiratory Distress Syndrome (ARDS) are especially devastating because lung damage is so critical and diff...

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Main Authors: Maira Soto, Gere diZerega, Kathleen E Rodgers
Format: Article
Language:English
Published: SAGE Publications 2020-11-01
Series:Journal of the Renin-Angiotensin-Aldosterone System
Online Access:https://doi.org/10.1177/1470320320972018
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author Maira Soto
Gere diZerega
Kathleen E Rodgers
author_facet Maira Soto
Gere diZerega
Kathleen E Rodgers
author_sort Maira Soto
collection DOAJ
description In the wake of the COVID-19 pandemic it has become clear that there is a need for therapies that are capable of reducing damage caused to patients from infections. Infections that induce Acute Respiratory Distress Syndrome (ARDS) are especially devastating because lung damage is so critical and difficult to manage. Angiotensin (1–7) [A(1–7)] has already been shown to protect pulmonary health and architecture in various models of disease. There is also evidence that A(1–7) can modulate immune function and protect various organs (lung, kidney, and heart) from oxidative damage and inflammation. Here we focus on making a case for the development of novel therapies that target the protective arm of the Renin Angiotensin System (RAS).
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spelling doaj.art-59a7627eba214318be3e192edf1045972024-03-02T10:28:32ZengSAGE PublicationsJournal of the Renin-Angiotensin-Aldosterone System1752-89762020-11-012110.1177/1470320320972018Countermeasure and therapeutic: A(1–7) to treat acute respiratory distress syndrome due to COVID-19 infectionMaira Soto0Gere diZerega1Kathleen E Rodgers2Department of Pharmacology, College of Medicine, Center for Innovation in Brain Science, University of Arizona, Tucson, AZ, USAUSBiotest, San Luis Obispo, CA, USADepartment of Pharmacology, College of Medicine, Center for Innovation in Brain Science, University of Arizona, Tucson, AZ, USAIn the wake of the COVID-19 pandemic it has become clear that there is a need for therapies that are capable of reducing damage caused to patients from infections. Infections that induce Acute Respiratory Distress Syndrome (ARDS) are especially devastating because lung damage is so critical and difficult to manage. Angiotensin (1–7) [A(1–7)] has already been shown to protect pulmonary health and architecture in various models of disease. There is also evidence that A(1–7) can modulate immune function and protect various organs (lung, kidney, and heart) from oxidative damage and inflammation. Here we focus on making a case for the development of novel therapies that target the protective arm of the Renin Angiotensin System (RAS).https://doi.org/10.1177/1470320320972018
spellingShingle Maira Soto
Gere diZerega
Kathleen E Rodgers
Countermeasure and therapeutic: A(1–7) to treat acute respiratory distress syndrome due to COVID-19 infection
Journal of the Renin-Angiotensin-Aldosterone System
title Countermeasure and therapeutic: A(1–7) to treat acute respiratory distress syndrome due to COVID-19 infection
title_full Countermeasure and therapeutic: A(1–7) to treat acute respiratory distress syndrome due to COVID-19 infection
title_fullStr Countermeasure and therapeutic: A(1–7) to treat acute respiratory distress syndrome due to COVID-19 infection
title_full_unstemmed Countermeasure and therapeutic: A(1–7) to treat acute respiratory distress syndrome due to COVID-19 infection
title_short Countermeasure and therapeutic: A(1–7) to treat acute respiratory distress syndrome due to COVID-19 infection
title_sort countermeasure and therapeutic a 1 7 to treat acute respiratory distress syndrome due to covid 19 infection
url https://doi.org/10.1177/1470320320972018
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