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Isochlorogenic acid C prevents enterovirus 71 infection via modulating redox homeostasis of glutathione
Enterovirus 71 (EV71) is a key pathogen of hand, foot and mouth disease (HFMD) in children under 6 years of age. The antiviral potency of antioxidant isochlorogenic acid C (ICAC) extracted from foods was evaluated in cellular and animal models. First, the cytotoxicity of ICAC on Vero cells was inves...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701158/ https://www.ncbi.nlm.nih.gov/pubmed/29176678 http://dx.doi.org/10.1038/s41598-017-16446-7 |
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author | Cao, Zeyu Ding, Yue Cao, Liang Ding, Gang Wang, Zhenzhong Xiao, Wei |
author_facet | Cao, Zeyu Ding, Yue Cao, Liang Ding, Gang Wang, Zhenzhong Xiao, Wei |
author_sort | Cao, Zeyu |
collection | PubMed |
description | Enterovirus 71 (EV71) is a key pathogen of hand, foot and mouth disease (HFMD) in children under 6 years of age. The antiviral potency of antioxidant isochlorogenic acid C (ICAC) extracted from foods was evaluated in cellular and animal models. First, the cytotoxicity of ICAC on Vero cells was investigated. The viral plaques, cytopathic effects and yield induced by EV71 infection were obviously reduced by ICAC, which was consistent with the investigation of VP1 transcripts and protein expression. Moreover, the mortality, weight loss and limb paralysis of mice caused by EV71 challenge were remarkably relieved by ICAC injection, which was achieved through decreases in the viral load and cytokine secretion in the mouse brain. Further biochemical assays showed that ICAC modulated several antioxidant enzymes involved in reduced and oxidized glutathione (GSH and GSSG) homeostasis, including glutathione reductase (GR), glutathione peroxidase (GPX), and glucose-6-phosphate dehydrogenase (G6PD), resulting in restoration of the GSH/GSSG ratio and reactive oxygen species (ROS) level. Finally, the antiviral effects of ICAC were dose-dependently disrupted by BSO, a biosynthesis inhibitor of GSH. This study indicated that ICAC acted as an antioxidant and prevented EV71 infection by modulating the redox homeostasis of glutathione. |
format | Online Article Text |
id | pubmed-5701158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57011582017-11-30 Isochlorogenic acid C prevents enterovirus 71 infection via modulating redox homeostasis of glutathione Cao, Zeyu Ding, Yue Cao, Liang Ding, Gang Wang, Zhenzhong Xiao, Wei Sci Rep Article Enterovirus 71 (EV71) is a key pathogen of hand, foot and mouth disease (HFMD) in children under 6 years of age. The antiviral potency of antioxidant isochlorogenic acid C (ICAC) extracted from foods was evaluated in cellular and animal models. First, the cytotoxicity of ICAC on Vero cells was investigated. The viral plaques, cytopathic effects and yield induced by EV71 infection were obviously reduced by ICAC, which was consistent with the investigation of VP1 transcripts and protein expression. Moreover, the mortality, weight loss and limb paralysis of mice caused by EV71 challenge were remarkably relieved by ICAC injection, which was achieved through decreases in the viral load and cytokine secretion in the mouse brain. Further biochemical assays showed that ICAC modulated several antioxidant enzymes involved in reduced and oxidized glutathione (GSH and GSSG) homeostasis, including glutathione reductase (GR), glutathione peroxidase (GPX), and glucose-6-phosphate dehydrogenase (G6PD), resulting in restoration of the GSH/GSSG ratio and reactive oxygen species (ROS) level. Finally, the antiviral effects of ICAC were dose-dependently disrupted by BSO, a biosynthesis inhibitor of GSH. This study indicated that ICAC acted as an antioxidant and prevented EV71 infection by modulating the redox homeostasis of glutathione. Nature Publishing Group UK 2017-11-24 /pmc/articles/PMC5701158/ /pubmed/29176678 http://dx.doi.org/10.1038/s41598-017-16446-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cao, Zeyu Ding, Yue Cao, Liang Ding, Gang Wang, Zhenzhong Xiao, Wei Isochlorogenic acid C prevents enterovirus 71 infection via modulating redox homeostasis of glutathione |
title | Isochlorogenic acid C prevents enterovirus 71 infection via modulating redox homeostasis of glutathione |
title_full | Isochlorogenic acid C prevents enterovirus 71 infection via modulating redox homeostasis of glutathione |
title_fullStr | Isochlorogenic acid C prevents enterovirus 71 infection via modulating redox homeostasis of glutathione |
title_full_unstemmed | Isochlorogenic acid C prevents enterovirus 71 infection via modulating redox homeostasis of glutathione |
title_short | Isochlorogenic acid C prevents enterovirus 71 infection via modulating redox homeostasis of glutathione |
title_sort | isochlorogenic acid c prevents enterovirus 71 infection via modulating redox homeostasis of glutathione |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701158/ https://www.ncbi.nlm.nih.gov/pubmed/29176678 http://dx.doi.org/10.1038/s41598-017-16446-7 |
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