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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. chinen...

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Autores principales: Ma, Juncheng, Wei, Juanru, Chen, Gang, Yan, Xiaowei, Sun, Hechun, Li, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10486283/
https://www.ncbi.nlm.nih.gov/pubmed/37675874
http://dx.doi.org/10.1080/13880209.2023.2253841
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author Ma, Juncheng
Wei, Juanru
Chen, Gang
Yan, Xiaowei
Sun, Hechun
Li, Ning
author_facet Ma, Juncheng
Wei, Juanru
Chen, Gang
Yan, Xiaowei
Sun, Hechun
Li, Ning
author_sort Ma, Juncheng
collection PubMed
description 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, EC(50): 259.3 μg/mL) and entry (EC(50): 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 (EC(50): 163.6 μg/mL), ethyl acetate (EC(50): 22.92 μg/mL) and n-butanol (EC(50): 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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spelling pubmed-104862832023-09-09 Extracts of Thesium chinense inhibit SARS-CoV-2 and inflammation in vitro Ma, Juncheng Wei, Juanru Chen, Gang Yan, Xiaowei Sun, Hechun Li, Ning Pharm Biol Research Article 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, EC(50): 259.3 μg/mL) and entry (EC(50): 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 (EC(50): 163.6 μg/mL), ethyl acetate (EC(50): 22.92 μg/mL) and n-butanol (EC(50): 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. Taylor & Francis 2023-09-07 /pmc/articles/PMC10486283/ /pubmed/37675874 http://dx.doi.org/10.1080/13880209.2023.2253841 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Article
Ma, Juncheng
Wei, Juanru
Chen, Gang
Yan, Xiaowei
Sun, Hechun
Li, Ning
Extracts of Thesium chinense inhibit SARS-CoV-2 and inflammation in vitro
title Extracts of Thesium chinense inhibit SARS-CoV-2 and inflammation in vitro
title_full Extracts of Thesium chinense inhibit SARS-CoV-2 and inflammation in vitro
title_fullStr Extracts of Thesium chinense inhibit SARS-CoV-2 and inflammation in vitro
title_full_unstemmed Extracts of Thesium chinense inhibit SARS-CoV-2 and inflammation in vitro
title_short Extracts of Thesium chinense inhibit SARS-CoV-2 and inflammation in vitro
title_sort extracts of thesium chinense inhibit sars-cov-2 and inflammation in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10486283/
https://www.ncbi.nlm.nih.gov/pubmed/37675874
http://dx.doi.org/10.1080/13880209.2023.2253841
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