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应对未来的大流行:基于 A 型原花青素的广谱抗病毒药物(BSAAs)。

Tackling the Future Pandemics: Broad-Spectrum Antiviral Agents (BSAAs) Based on A-Type Proanthocyanidins.

机构信息

Department of Life Sciences and Systems Biology, University of Turin, Via Quarello 15/a, 10135 Turin, Italy.

Department of Molecular Medicine, University of Padua, 35121 Padua, Italy.

出版信息

Molecules. 2022 Nov 30;27(23):8353. doi: 10.3390/molecules27238353.

Abstract

A-type proanthocyanidins (PAC-As) are plant-derived natural polyphenols that occur as oligomers or polymers of flavan-3-ol monomers, such as (+)-catechin and (-)-epicatechin, connected through an unusual double A linkage. PAC-As are present in leaves, seeds, flowers, bark, and fruits of many plants, and are thought to exert protective natural roles against microbial pathogens, insects, and herbivores. Consequently, when tested in isolation, PAC-As have shown several biological effects, through antioxidant, antibacterial, immunomodulatory, and antiviral activities. PAC-As have been observed in fact to inhibit replication of many different human viruses, and both enveloped and non-enveloped DNA and RNA viruses proved sensible to their inhibitory effect. Mechanistic studies revealed that PAC-As cause reduction of infectivity of viral particles they come in contact with, as a result of their propensity to interact with virion surface capsid proteins or envelope glycoproteins essential for viral attachment and entry. As viral infections and new virus outbreaks are a major public health concern, development of effective Broad-Spectrum Antiviral Agents (BSAAs) that can be rapidly deployable even against future emerging viruses is an urgent priority. This review summarizes the antiviral activities and mechanism of action of PAC-As, and their potential to be deployed as BSAAs against present and future viral infections.

摘要

A型原花青素(PAC-As)是植物来源的天然多酚类化合物,以黄烷-3-醇单体(如(+)-儿茶素和(-)-表儿茶素)的低聚物或聚合物形式存在,通过不寻常的双 A 键连接。PAC-As 存在于许多植物的叶、种子、花、树皮和果实中,被认为对微生物病原体、昆虫和草食动物具有保护天然作用。因此,当单独测试时,PAC-As 表现出多种生物学效应,通过抗氧化、抗菌、免疫调节和抗病毒活性。事实上,已经观察到 PAC-As 抑制许多不同人类病毒的复制,并且包膜和非包膜 DNA 和 RNA 病毒都对其抑制作用敏感。机制研究表明,PAC-As 导致其接触的病毒颗粒感染性降低,这是由于它们与病毒衣壳表面衣壳蛋白或包膜糖蛋白相互作用的倾向,这些蛋白对于病毒附着和进入至关重要。由于病毒感染和新的病毒爆发是一个主要的公共卫生关注点,因此开发有效的广谱抗病毒药物(BSAAs),即使针对未来出现的新兴病毒也能迅速部署,这是当务之急。本综述总结了 PAC-As 的抗病毒活性和作用机制,以及将其作为 BSAAs 用于当前和未来病毒感染的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/905f/9736452/3ad5c4f5e87d/molecules-27-08353-g001.jpg

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