反调节肾素-血管紧张素系统:COVID-19领域中一个意想不到的盟友。

The Counter-Regulatory Renin-Angiotensin System: A Surprising Ally in the Field of COVID-19.

作者信息

Palacios Cruz Mariali, Castellar-Lopez Jairo, Manuel Pretelt Juan, Y Chang Aileen, Mendoza-Torres Evelyn

机构信息

Grupo de Investigación Avanzada en Biomedicina, Faculty of Health, Exact and Natural Sciences. Universidad Libre Seccional Barranquilla, Barranquilla, Colombia.

Internal Medicine Program, Faculty of Health, Exact and Natural Sciences, Universidad Libre de Colombia, Seccional Barranquilla-Colombia.

出版信息

Infect Disord Drug Targets. 2025 Jul 30. doi: 10.2174/0118715265352715250717101135.

Abstract

INTRODUCTION

Over the past four years, SARS-CoV-2 and COVID-19 have become global health crises, spurring extensive research on virus behavior, complications, and treatments. The virus interacts with a component of the renin-angiotensin system (RAS), altering inflammatory, hyper-trophic, and hemodynamic responses via binding to ACE2 found in organs like the heart, lungs, and kidneys.

OBJECTIVE

This review explores the RAS-COVID-19 interplay, focusing on key molecules like ACE2, Ang-(1-7), and Ang-(1-9), influencing susceptibility, severity, and treatments. It seeks to clar-ify ACE2's dual role in viral entry and protection and assess the therapeutic potential of balancing Ang-(1-7) and Ang-(1-9) to prevent disease progression and related complications.

METHODS

Studies were chosen through a systematic search in databases, such as PubMed, Scopus, and Web of Science. The inclusion criteria were centered on peer-reviewed research that explored the relationship between SARS-CoV-2 and important RAS molecules, including ACE2, Ang-(1-7), and Ang-(1-9), seeking information on therapies, severity, and susceptibility. Non-peer-reviewed ar-ticles and those lacking focus on RAS-COVID-19 interplay were excluded. Titles and abstracts were screened, followed by full-text assessment and data extraction for analysis Results: Some studies indicate that the peptides Ang-(1-7) and Ang-(1-9) could provide protective effects against heart-related complications by counteracting the harmful impacts of the angiotensin II pathway, which is often exacerbated by SARS-CoV-2. Ang-(1-7) and Ang-(1-9) are recognized for promoting vasodilation, reducing inflammation, and preventing fibrosis, which can mitigate the heart damage typically associated with COVID-19.

DISCUSSION

ACE2, a component of the non-canonical RAS, is closely linked to SARS-CoV-2 and plays a pivotal role in the pathophysiology of COVID-19. Ang-(1-9) and Ang-(1-7) are produced by ACE2 and have demonstrated positive cardiovascular effects. In the context of COVID-19, Ang-(1-7) has shown protective effects in preclinical studies and clinical trials; however, more evidence is needed to support this effect.

CONCLUSION

Further research, including clinical trials, is vital to understand and develop precise therapies for COVID-19 and similar infectious diseases.

摘要

引言

在过去四年中,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)和冠状病毒病(COVID-19)已成为全球健康危机,激发了对病毒行为、并发症和治疗方法的广泛研究。该病毒与肾素-血管紧张素系统(RAS)的一个成分相互作用,通过与心脏、肺和肾脏等器官中发现的血管紧张素转换酶2(ACE2)结合,改变炎症、肥大和血流动力学反应。

目的

本综述探讨RAS与COVID-19之间的相互作用,重点关注ACE2、血管紧张素(1-7)[Ang-(1-7)]和血管紧张素(1-9)[Ang-(1-9)]等关键分子,这些分子会影响易感性、疾病严重程度和治疗方法。本综述旨在阐明ACE2在病毒进入和保护方面的双重作用,并评估平衡Ang-(1-7)和Ang-(1-9)以预防疾病进展和相关并发症的治疗潜力。

方法

通过在PubMed、Scopus和Web of Science等数据库中进行系统检索来选择研究。纳入标准集中在同行评审的研究上,这些研究探讨了SARS-CoV-2与重要的RAS分子(包括ACE2、Ang-(1-7)和Ang-(1-9))之间的关系,以获取有关治疗方法、疾病严重程度和易感性的信息。非同行评审的文章以及那些未关注RAS与COVID-19相互作用的文章被排除。先筛选标题和摘要,然后进行全文评估和数据提取以进行分析。结果:一些研究表明,Ang-(1-7)和Ang-(1-9)肽可以通过抵消血管紧张素II途径的有害影响来预防与心脏相关的并发症,而血管紧张素II途径通常会因SARS-CoV-2而加剧。Ang-(1-7)和Ang-(1-9)因能促进血管舒张、减轻炎症和预防纤维化而闻名,这些作用可以减轻通常与COVID-19相关的心脏损伤。

讨论

ACE2作为非经典RAS的一个成分,与SARS-CoV-2密切相关,在COVID-19的病理生理学中起关键作用。Ang-(1-9)和Ang-(1-7)由ACE2产生,并已证明具有积极的心血管效应。在COVID-19的背景下,Ang-(1-7)在临床前研究和临床试验中已显示出保护作用;然而,还需要更多证据来支持这一作用。

结论

包括临床试验在内的进一步研究对于理解和开发针对COVID-19及类似传染病的精确治疗方法至关重要。

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