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Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro

Stress has been proven to modulate an individual’s immune system through the release of pituitary and adrenal hormones such as the catecholamines, growth hormone, and glucocorticoids. These signal molecules can significantly alter the host immune system and make it susceptible to viral infection. In...

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Autores principales: Luo, Zhuo, Liu, Li-Fang, Wang, Xiao-Hua, Li, Wen, Jie, Chong, Chen, Huan, Wei, Fan-Qin, Lu, Dan-Hua, Yan, Chang-Yu, Liu, Bo, Kurihara, Hiroshi, Li, Yi-Fang, He, Rong-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374342/
https://www.ncbi.nlm.nih.gov/pubmed/30792656
http://dx.doi.org/10.3389/fphar.2019.00078
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author Luo, Zhuo
Liu, Li-Fang
Wang, Xiao-Hua
Li, Wen
Jie, Chong
Chen, Huan
Wei, Fan-Qin
Lu, Dan-Hua
Yan, Chang-Yu
Liu, Bo
Kurihara, Hiroshi
Li, Yi-Fang
He, Rong-Rong
author_facet Luo, Zhuo
Liu, Li-Fang
Wang, Xiao-Hua
Li, Wen
Jie, Chong
Chen, Huan
Wei, Fan-Qin
Lu, Dan-Hua
Yan, Chang-Yu
Liu, Bo
Kurihara, Hiroshi
Li, Yi-Fang
He, Rong-Rong
author_sort Luo, Zhuo
collection PubMed
description Stress has been proven to modulate an individual’s immune system through the release of pituitary and adrenal hormones such as the catecholamines, growth hormone, and glucocorticoids. These signal molecules can significantly alter the host immune system and make it susceptible to viral infection. In this study, we investigate whether epigoitrin, a natural alkaloid from Isatis indigotica, provides protection against influenza infection by reducing the host’s susceptibility to influenza virus under stress and its underlying mechanism. To support it, the mouse restraint stress model and the corticosterone-induced stress model were employed. Our results demonstrated that epigoitrin significantly decreased the susceptibility of restraint mice to influenza virus, evidenced by lowered mortality, attenuated inflammation, and decreased viral replications in lungs. Further results revealed that epigoitrin reduced the protein expression of mitofusin-2 (MFN2), which elevated mitochondria antiviral signaling (MAVS) protein expression and subsequently increased the production of IFN-β and interferon inducible transmembrane 3 (IFITM3), thereby helping to fight viral infections. In conclusion, our study indicated that epigoitrin could reduce the susceptibility to influenza virus via mitochondrial antiviral signaling.
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spelling pubmed-63743422019-02-21 Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro Luo, Zhuo Liu, Li-Fang Wang, Xiao-Hua Li, Wen Jie, Chong Chen, Huan Wei, Fan-Qin Lu, Dan-Hua Yan, Chang-Yu Liu, Bo Kurihara, Hiroshi Li, Yi-Fang He, Rong-Rong Front Pharmacol Pharmacology Stress has been proven to modulate an individual’s immune system through the release of pituitary and adrenal hormones such as the catecholamines, growth hormone, and glucocorticoids. These signal molecules can significantly alter the host immune system and make it susceptible to viral infection. In this study, we investigate whether epigoitrin, a natural alkaloid from Isatis indigotica, provides protection against influenza infection by reducing the host’s susceptibility to influenza virus under stress and its underlying mechanism. To support it, the mouse restraint stress model and the corticosterone-induced stress model were employed. Our results demonstrated that epigoitrin significantly decreased the susceptibility of restraint mice to influenza virus, evidenced by lowered mortality, attenuated inflammation, and decreased viral replications in lungs. Further results revealed that epigoitrin reduced the protein expression of mitofusin-2 (MFN2), which elevated mitochondria antiviral signaling (MAVS) protein expression and subsequently increased the production of IFN-β and interferon inducible transmembrane 3 (IFITM3), thereby helping to fight viral infections. In conclusion, our study indicated that epigoitrin could reduce the susceptibility to influenza virus via mitochondrial antiviral signaling. Frontiers Media S.A. 2019-02-07 /pmc/articles/PMC6374342/ /pubmed/30792656 http://dx.doi.org/10.3389/fphar.2019.00078 Text en Copyright © 2019 Luo, Liu, Wang, Li, Jie, Chen, Wei, Lu, Yan, Liu, Kurihara, Li and He. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Luo, Zhuo
Liu, Li-Fang
Wang, Xiao-Hua
Li, Wen
Jie, Chong
Chen, Huan
Wei, Fan-Qin
Lu, Dan-Hua
Yan, Chang-Yu
Liu, Bo
Kurihara, Hiroshi
Li, Yi-Fang
He, Rong-Rong
Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro
title Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro
title_full Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro
title_fullStr Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro
title_full_unstemmed Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro
title_short Epigoitrin, an Alkaloid From Isatis indigotica, Reduces H1N1 Infection in Stress-Induced Susceptible Model in vivo and in vitro
title_sort epigoitrin, an alkaloid from isatis indigotica, reduces h1n1 infection in stress-induced susceptible model in vivo and in vitro
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6374342/
https://www.ncbi.nlm.nih.gov/pubmed/30792656
http://dx.doi.org/10.3389/fphar.2019.00078
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