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Antiviral Activities of Quercetin and Isoquercitrin Against Human Herpesviruses

We previously reported that the ethyl acetate (EtOAc) fraction of a 70% ethanol extract of Elaeocarpus sylvestris (ESE) inhibits varicella-zoster virus (VZV) and human cytomegalovirus (HCMV) replication in vitro. PGG (1,2,3,4,6-penta-O-galloyl-ß-D-glucose) is a major chemical constituent of the EtOA...

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Autores principales: Kim, Chae Hyun, Kim, Jung-Eun, Song, Yoon-Jae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287991/
https://www.ncbi.nlm.nih.gov/pubmed/32443914
http://dx.doi.org/10.3390/molecules25102379
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author Kim, Chae Hyun
Kim, Jung-Eun
Song, Yoon-Jae
author_facet Kim, Chae Hyun
Kim, Jung-Eun
Song, Yoon-Jae
author_sort Kim, Chae Hyun
collection PubMed
description We previously reported that the ethyl acetate (EtOAc) fraction of a 70% ethanol extract of Elaeocarpus sylvestris (ESE) inhibits varicella-zoster virus (VZV) and human cytomegalovirus (HCMV) replication in vitro. PGG (1,2,3,4,6-penta-O-galloyl-ß-D-glucose) is a major chemical constituent of the EtOAc fraction of ESE that inhibits VZV but not HCMV replication. In this study, we comprehensively screened the chemical compounds identified in the EtOAc fraction of ESE for potential antiviral properties. Among the examined compounds, quercetin and isoquercitrin displayed potent antiviral activities against both VZV and HCMV with no significant cytotoxic effects. Both compounds strongly suppressed the expression of VZV and HCMV immediate–early (IE) genes. Our collective results indicated that, in addition to PGG, quercetin and isoquercitrin are bioactive compounds in the EtOAc fraction of ESE that effectively inhibit human herpesvirus replication.
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spelling pubmed-72879912020-06-15 Antiviral Activities of Quercetin and Isoquercitrin Against Human Herpesviruses Kim, Chae Hyun Kim, Jung-Eun Song, Yoon-Jae Molecules Article We previously reported that the ethyl acetate (EtOAc) fraction of a 70% ethanol extract of Elaeocarpus sylvestris (ESE) inhibits varicella-zoster virus (VZV) and human cytomegalovirus (HCMV) replication in vitro. PGG (1,2,3,4,6-penta-O-galloyl-ß-D-glucose) is a major chemical constituent of the EtOAc fraction of ESE that inhibits VZV but not HCMV replication. In this study, we comprehensively screened the chemical compounds identified in the EtOAc fraction of ESE for potential antiviral properties. Among the examined compounds, quercetin and isoquercitrin displayed potent antiviral activities against both VZV and HCMV with no significant cytotoxic effects. Both compounds strongly suppressed the expression of VZV and HCMV immediate–early (IE) genes. Our collective results indicated that, in addition to PGG, quercetin and isoquercitrin are bioactive compounds in the EtOAc fraction of ESE that effectively inhibit human herpesvirus replication. MDPI 2020-05-20 /pmc/articles/PMC7287991/ /pubmed/32443914 http://dx.doi.org/10.3390/molecules25102379 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Chae Hyun
Kim, Jung-Eun
Song, Yoon-Jae
Antiviral Activities of Quercetin and Isoquercitrin Against Human Herpesviruses
title Antiviral Activities of Quercetin and Isoquercitrin Against Human Herpesviruses
title_full Antiviral Activities of Quercetin and Isoquercitrin Against Human Herpesviruses
title_fullStr Antiviral Activities of Quercetin and Isoquercitrin Against Human Herpesviruses
title_full_unstemmed Antiviral Activities of Quercetin and Isoquercitrin Against Human Herpesviruses
title_short Antiviral Activities of Quercetin and Isoquercitrin Against Human Herpesviruses
title_sort antiviral activities of quercetin and isoquercitrin against human herpesviruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7287991/
https://www.ncbi.nlm.nih.gov/pubmed/32443914
http://dx.doi.org/10.3390/molecules25102379
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