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基于生物信息学分析及对脂多糖刺激巨噬细胞的药理作用,茶成分具有抗2019冠状病毒病(COVID-19)靶点。

Tea Ingredients Have Anti-coronavirus Disease 2019 (COVID-19) Targets Based on Bioinformatics Analyses and Pharmacological Effects on LPS-Stimulated Macrophages.

作者信息

Wang Lei, Tao Qing, Wang Zhiguo, Shi Jianfeng, Yan Wei, Zhang Li, Sun Yaoxiang, Yao Xiaoming

机构信息

Department of Clinical Laboratory, Jiangsu Province Hospital on Integration of Chinese and Western Medicine, Jiangsu Province Academy of Traditional Chinese Medicine, Nanjing, China.

Center for Translational Medicine and Jiangsu Key Laboratory of Molecular Medicine, Department of Basic Medicine, Medical School of Nanjing University, Nanjing, China.

出版信息

Front Nutr. 2022 May 20;9:875765. doi: 10.3389/fnut.2022.875765. eCollection 2022.

DOI:10.3389/fnut.2022.875765
PMID:35669076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9163550/
Abstract

Coronavirus disease 2019 (COVID-19) is a contagious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that caused millions of deaths and lacks treatment. Although several studies have focused on the major component of green tea, epigallocatechin 3-gallate (EGCG), which is efficient in preventing COVID-19, systemic analyses of the anti-COVID-19 potential of green tea remain insufficient. Here, we co-analyzed the target genes of tea ingredients and COVID-19 signature genes and found that epigallocatechin 3-acetalbehyde was capable of reversing the major molecular processes of COVID-19 (MAPK and NF-κB activation). These findings were further supported by Western blotting (WB), immunofluorescence, and quantitative polymerase chain reaction (qPCR) in LPS-stimulated macrophages. Moreover, using molecular docking analysis, we identified three tea ingredients ((-)-catechin gallate, D-(+)-cellobiose, and EGCG) that may interact with the vital SARS-CoV-2 protein, 5R84, compared with the qualified 5R84 ligand WGS. Thus, our results indicated that tea ingredients have the potential to treat COVID-19 by suppressing the COVID-19 signature genes and interacting with the vital SARS-CoV-2 protein.

摘要

2019冠状病毒病(COVID-19)是一种由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的传染病,已导致数百万人死亡且缺乏治疗方法。尽管有几项研究聚焦于绿茶的主要成分表没食子儿茶素没食子酸酯(EGCG),其在预防COVID-19方面具有功效,但对绿茶抗COVID-19潜力的系统分析仍然不足。在此,我们共同分析了茶成分的靶基因和COVID-19特征基因,发现表没食子儿茶素3 - 乙醛能够逆转COVID-19的主要分子过程(丝裂原活化蛋白激酶和核因子κB激活)。在脂多糖刺激的巨噬细胞中进行的蛋白质印迹法(WB)、免疫荧光和定量聚合酶链反应(qPCR)进一步支持了这些发现。此外,通过分子对接分析,我们鉴定出三种茶成分((-)-儿茶素没食子酸酯、D-(+)-纤维二糖和EGCG),与合格的5R84配体WGS相比,它们可能与重要的SARS-CoV-2蛋白5R84相互作用。因此,我们的结果表明茶成分有可能通过抑制COVID-19特征基因并与重要的SARS-CoV-2蛋白相互作用来治疗COVID-19。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/6244cec9f9da/fnut-09-875765-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/3ac5c3d50d5e/fnut-09-875765-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/f10190495960/fnut-09-875765-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/8e56259df22a/fnut-09-875765-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/ae56ff05a46a/fnut-09-875765-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/6244cec9f9da/fnut-09-875765-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/3ac5c3d50d5e/fnut-09-875765-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/f10190495960/fnut-09-875765-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/8e56259df22a/fnut-09-875765-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/ae56ff05a46a/fnut-09-875765-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b14/9163550/6244cec9f9da/fnut-09-875765-g0005.jpg

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