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Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms

Due to the scarcity of therapeutic approaches for COVID-19, we investigated the antiviral and anti-inflammatory properties of curcumin against SARS-CoV-2 using in vitro models. The cytotoxicity of curcumin was evaluated using MTT assay in Vero E6 cells. The antiviral activity of this compound agains...

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Autores principales: Marín-Palma, Damariz, Tabares-Guevara, Jorge H., Zapata-Cardona, María I., Flórez-Álvarez, Lizdany, Yepes, Lina M., Rugeles, Maria T., Zapata-Builes, Wildeman, Hernandez, Juan C., Taborda, Natalia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618354/
https://www.ncbi.nlm.nih.gov/pubmed/34833991
http://dx.doi.org/10.3390/molecules26226900
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author Marín-Palma, Damariz
Tabares-Guevara, Jorge H.
Zapata-Cardona, María I.
Flórez-Álvarez, Lizdany
Yepes, Lina M.
Rugeles, Maria T.
Zapata-Builes, Wildeman
Hernandez, Juan C.
Taborda, Natalia A.
author_facet Marín-Palma, Damariz
Tabares-Guevara, Jorge H.
Zapata-Cardona, María I.
Flórez-Álvarez, Lizdany
Yepes, Lina M.
Rugeles, Maria T.
Zapata-Builes, Wildeman
Hernandez, Juan C.
Taborda, Natalia A.
author_sort Marín-Palma, Damariz
collection PubMed
description Due to the scarcity of therapeutic approaches for COVID-19, we investigated the antiviral and anti-inflammatory properties of curcumin against SARS-CoV-2 using in vitro models. The cytotoxicity of curcumin was evaluated using MTT assay in Vero E6 cells. The antiviral activity of this compound against SARS-CoV-2 was evaluated using four treatment strategies (i. pre–post infection treatment, ii. co-treatment, iii. pre-infection, and iv. post-infection). The D614G strain and Delta variant of SARS-CoV-2 were used, and the viral titer was quantified by plaque assay. The anti-inflammatory effect was evaluated in peripheral blood mononuclear cells (PBMCs) using qPCR and ELISA. By pre–post infection treatment, Curcumin (10 µg/mL) exhibited antiviral effect of 99% and 99.8% against DG614 strain and Delta variant, respectively. Curcumin also inhibited D614G strain by pre-infection and post-infection treatment. In addition, curcumin showed a virucidal effect against D614G strain and Delta variant. Finally, the pro-inflammatory cytokines (IL-1β, IL-6, and IL-8) released by PBMCs triggered by SARS-CoV-2 were decreased after treatment with curcumin. Our results suggest that curcumin affects the SARS-CoV-2 replicative cycle and exhibits virucidal effect with a variant/strain independent antiviral effect and immune-modulatory properties. This is the first study that showed a combined (antiviral/anti-inflammatory) effect of curcumin during SARS-CoV-2 infection. However, additional studies are required to define its use as a treatment for the COVID-19.
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spelling pubmed-86183542021-11-27 Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms Marín-Palma, Damariz Tabares-Guevara, Jorge H. Zapata-Cardona, María I. Flórez-Álvarez, Lizdany Yepes, Lina M. Rugeles, Maria T. Zapata-Builes, Wildeman Hernandez, Juan C. Taborda, Natalia A. Molecules Article Due to the scarcity of therapeutic approaches for COVID-19, we investigated the antiviral and anti-inflammatory properties of curcumin against SARS-CoV-2 using in vitro models. The cytotoxicity of curcumin was evaluated using MTT assay in Vero E6 cells. The antiviral activity of this compound against SARS-CoV-2 was evaluated using four treatment strategies (i. pre–post infection treatment, ii. co-treatment, iii. pre-infection, and iv. post-infection). The D614G strain and Delta variant of SARS-CoV-2 were used, and the viral titer was quantified by plaque assay. The anti-inflammatory effect was evaluated in peripheral blood mononuclear cells (PBMCs) using qPCR and ELISA. By pre–post infection treatment, Curcumin (10 µg/mL) exhibited antiviral effect of 99% and 99.8% against DG614 strain and Delta variant, respectively. Curcumin also inhibited D614G strain by pre-infection and post-infection treatment. In addition, curcumin showed a virucidal effect against D614G strain and Delta variant. Finally, the pro-inflammatory cytokines (IL-1β, IL-6, and IL-8) released by PBMCs triggered by SARS-CoV-2 were decreased after treatment with curcumin. Our results suggest that curcumin affects the SARS-CoV-2 replicative cycle and exhibits virucidal effect with a variant/strain independent antiviral effect and immune-modulatory properties. This is the first study that showed a combined (antiviral/anti-inflammatory) effect of curcumin during SARS-CoV-2 infection. However, additional studies are required to define its use as a treatment for the COVID-19. MDPI 2021-11-16 /pmc/articles/PMC8618354/ /pubmed/34833991 http://dx.doi.org/10.3390/molecules26226900 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Marín-Palma, Damariz
Tabares-Guevara, Jorge H.
Zapata-Cardona, María I.
Flórez-Álvarez, Lizdany
Yepes, Lina M.
Rugeles, Maria T.
Zapata-Builes, Wildeman
Hernandez, Juan C.
Taborda, Natalia A.
Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms
title Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms
title_full Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms
title_fullStr Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms
title_full_unstemmed Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms
title_short Curcumin Inhibits In Vitro SARS-CoV-2 Infection In Vero E6 Cells through Multiple Antiviral Mechanisms
title_sort curcumin inhibits in vitro sars-cov-2 infection in vero e6 cells through multiple antiviral mechanisms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618354/
https://www.ncbi.nlm.nih.gov/pubmed/34833991
http://dx.doi.org/10.3390/molecules26226900
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