莱菔硫烷
机制(生物学)
因子(编程语言)
化学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019年冠状病毒病(COVID-19)
病毒学
生物
医学
生物化学
内科学
物理
计算机科学
疾病
量子力学
传染病(医学专业)
程序设计语言
作者
Ziqi Yan,Weifeng Liang,Lingxiang Zhu,Ivana Kreso,Venesa Romero,Melisa Smith,Yin Chen
标识
DOI:10.35534/jrbtm.2024.10010
摘要
It is well established that Nrf2 plays a crucial role in anti-oxidant and anti-inflammatory functions. However, its antiviral capabilities remain less explored. Despite this, several Nrf2 activators have demonstrated anti-SARS-CoV-2 properties, though the mechanisms behind these effects are not fully understood. In this study, using two mouse models of SARS-CoV-2 infection, we observed that the absence of Nrf2 significantly increased viral load and altered inflammatory responses. Additionally, we evaluated five Nrf2 modulators. Notably, epigallocatechin gallate (EGCG), sulforaphane (SFN), and dimethyl fumarate (DMF) exhibited significant antiviral effects, with SFN being the most effective. SFN did not impact viral entry but appeared to inhibit the main protease (M
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