中国梧桐提取物体外抑制SARS-CoV-2和炎症。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-09-07 DOI:10.1080/13880209.2023.2253841
Juncheng Ma, Juanru Wei, Gang Chen, Xiaowei Yan, Hechun Sun, Ning Li
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摘要

背景:严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)仍在快速传播。目前,尚没有相关的研究基于桑草科植物Thesium chinense Turcz抗病毒作用。目的:研究黄芪提取物的抗病毒和抗炎作用。材料与方法:研究三叶草乙醇提取物(药物浓度分别为80、160、320、640、960 μg/mL)对SARS-CoV-2的抗进入和复制作用。以Remdesivir (20.74 μM)为阳性对照,以Vero细胞为宿主细胞,采用实时定量聚合酶链反应(RT-PCR)和Western blotting检测病毒核衣壳蛋白(NP)的表达水平。将RAW264.7细胞作为脂多糖(LPS)诱导下的抗炎实验模型,采用酶联免疫吸附法(ELISA)检测其肿瘤坏死因子-α (TNF-α)和白细胞介素-6 (IL-6)的表达水平。结果:三叶草乙醇提取物显著抑制SARS-CoV-2复制(最大有效浓度的一半,EC50: 259.3 μg/mL)和进入Vero细胞(EC50: 359.1 μg/mL),显著降低lps刺激RAW264.7细胞产生的IL-6和TNF-α水平。石油醚(EC50: 163.6 μg/mL)、乙酸乙酯(EC50: 22.92 μg/mL)和正丁醇(EC50: 56.8 μg/mL)提取物对Vero细胞的SARS-CoV-2复制有较弱的抑制作用,并降低lps刺激RAW264.7细胞产生的IL-6和TNF-α水平。结论:中华弓形虫可能是抗SARS-CoV-2的潜在候选药物,并正在成为治疗COVID-19的候选中药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Extracts of Thesium chinense inhibit SARS-CoV-2 and inflammation in vitro.

Context: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is still spreading rapidly. Relevant research based on the antiviral effects of Thesium chinense Turcz (Santalaceae) was not found.

Objective: To investigate the antiviral and anti-inflammatory effects of extracts of T. chinense.

Materials and methods: To investigate the anti-entry and replication effect of the ethanol extract of T. chinense (drug concentration 80, 160, 320, 640, 960 μg/mL) against the SARS-CoV-2. Remdesivir (20.74 μM) was used as positive control, and Vero cells were used as host cells to detect the expression level of nucleocapsid protein (NP) in the virus by real-time quantitative polymerase chain reaction (RT-PCR) and Western blotting. RAW264.7 cells were used as an anti-inflammatory experimental model under lipopolysaccharide (LPS) induction, and the expression levels of tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6) were detected by enzyme-linked immunosorbent assay (ELISA).

Results: The ethanol extract of T. chinense significantly inhibited the replication (half maximal effective concentration, EC50: 259.3 μg/mL) and entry (EC50: 359.1 μg/mL) of SARS-CoV-2 into Vero cells, and significantly reduced the levels of IL-6 and TNF-α produced by LPS-stimulated RAW264.7 cells. Petroleum ether (EC50: 163.6 μg/mL), ethyl acetate (EC50: 22.92 μg/mL) and n-butanol (EC50: 56.8 μg/mL) extracts showed weak inhibition of SARS-CoV-2 replication in Vero cells, and reduced the levels of IL-6 and TNF-α produced by LPS-stimulated RAW264.7 cells.

Conclusion: T. chinense can be a potential candidate to fight SARS-CoV-2, and is becoming a traditional Chinese medicine candidate for treating COVID-19.

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