Soto Maira, diZerega Gere, Rodgers Kathleen E
Department of Pharmacology, College of Medicine, Center for Innovation in Brain Science, University of Arizona, Tucson, AZ, USA.
USBiotest, San Luis Obispo, CA, USA.
J Renin Angiotensin Aldosterone Syst. 2020 Oct-Dec;21(4):1470320320972018. doi: 10.1177/1470320320972018.
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).
在新冠疫情之后,很明显需要有能够减少感染对患者造成损害的疗法。引发急性呼吸窘迫综合征(ARDS)的感染尤其具有破坏性,因为肺部损伤非常严重且难以处理。血管紧张素(1-7)[A(1-7)]已在多种疾病模型中显示出对肺部健康和结构具有保护作用。也有证据表明,A(1-7)可以调节免疫功能,并保护各个器官(肺、肾和心脏)免受氧化损伤和炎症侵害。在此,我们着重阐述开发针对肾素血管紧张素系统(RAS)保护分支的新型疗法的理由。