反调节性肾素-血管紧张素系统:COVID-19领域的惊人盟友。

Mariali Palacios Cruz, Jairo Castellar-Lopez, Juan Manuel Pretelt, Aileen Y Chang, Evelyn Mendoza-Torres
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引用次数: 0

摘要

在过去四年中,SARS-CoV-2和COVID-19已成为全球健康危机,促使人们对病毒行为、并发症和治疗进行了广泛的研究。该病毒与肾素-血管紧张素系统(RAS)的一种成分相互作用,通过与心脏、肺和肾脏等器官中的ACE2结合,改变炎症、肥厚和血流动力学反应。目的:探讨RAS-COVID-19相互作用,重点关注ACE2、Ang-(1-7)、Ang-(1-9)等关键分子对易感性、严重程度和治疗的影响。该研究旨在阐明ACE2在病毒进入和保护中的双重作用,并评估平衡Ang-(1-7)和Ang-(1-9)预防疾病进展和相关并发症的治疗潜力。方法:通过系统检索PubMed、Scopus和Web of Science等数据库选择研究。纳入标准以同行评议的研究为中心,这些研究探讨了SARS-CoV-2与重要RAS分子(包括ACE2、Ang-(1-7)和Ang-(1-9))之间的关系,以寻求有关治疗、严重程度和易感性的信息。未经过同行评审的文章和缺乏对RAS-COVID-19相互作用的关注的文章被排除在外。结果:一些研究表明,肽Ang-(1-7)和Ang-(1-9)可通过抵消血管紧张素II通路的有害影响,对心脏相关并发症提供保护作用,而血管紧张素II通路通常会因SARS-CoV-2而加剧。Ang-(1-7)和Ang-(1-9)被认为可以促进血管舒张、减少炎症和预防纤维化,从而减轻与COVID-19相关的心脏损伤。讨论:ACE2是非规范RAS的一个组成部分,与SARS-CoV-2密切相关,在COVID-19的病理生理中发挥关键作用。Ang-(1-9)和Ang-(1-7)由ACE2产生,并显示出积极的心血管作用。在COVID-19背景下,Ang-(1-7)在临床前研究和临床试验中显示出保护作用;然而,需要更多的证据来支持这种效果。结论:进一步的研究,包括临床试验,对于了解和开发COVID-19和类似传染病的精确治疗方法至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Counter-Regulatory Renin-Angiotensin System: A Surprising Ally in the Field of COVID-19.

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.

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