Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways

Yinghua Li,* Zhengfang Lin,* Min Guo, Mingqi Zhao, Yu Xia, Changbing Wang, Tiantian Xu, Bing Zhu Center Laboratory, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China *These authors contributed equally to this work Introduction: As a therapeuti...

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Autores principales: Li Y, Lin Z, Guo M, Zhao M, Xia Y, Wang C, Xu T, Zhu B
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Publicado: Dove Medical Press 2018
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spelling oai:doaj.org-article:6c60bda584094bb5885a5e409d69e0742021-12-02T04:47:11ZInhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways1178-2013https://doaj.org/article/6c60bda584094bb5885a5e409d69e0742018-04-01T00:00:00Zhttps://www.dovepress.com/inhibition-of-h1n1-influenza-virus-induced-apoptosis-by-functionalized-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Yinghua Li,* Zhengfang Lin,* Min Guo, Mingqi Zhao, Yu Xia, Changbing Wang, Tiantian Xu, Bing Zhu Center Laboratory, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China *These authors contributed equally to this work Introduction: As a therapeutic antiviral agent, the clinical application of amantadine (AM) is limited by the emergence of drug-resistant viruses. To overcome the drug-resistant viruses and meet the growing demand of clinical diagnosis, the use of biological nanoparticles (NPs) has increased in order to develop novel anti-influenza drugs. The antiviral activity of selenium NPs with low toxicity and excellent activities has attracted increasing attention for biomedical intervention in recent years.Methods and results: In the present study, surface decoration of selenium NPs by AM (Se@AM) was designed to reverse drug resistance caused by influenza virus infection. Se@AM with less toxicity remarkably inhibited the ability of H1N1 influenza to infect host cells through suppression of the neuraminidase activity. Moreover, Se@AM could prevent H1N1 from infecting Madin Darby Canine Kidney cell line and causing cell apoptosis supported by DNA fragmentation and chromatin condensation. Furthermore, Se@AM obviously inhibited the generation of reactive oxygen species and activation of phosphorylation of AKT.Conclusion: These results demonstrate that Se@AM is a potentially efficient antiviral pharmaceutical agent for H1N1 influenza virus. Keywords: selenium nanoparticles, amantadine, influenza virus, apoptosis, nanodrugLi YLin ZGuo MZhao MXia YWang CXu TZhu BDove Medical PressarticleSelenium nanoparticlesAmantadineInfluenza virusApoptosisMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 13, Pp 2005-2016 (2018)
institution DOAJ
collection DOAJ
language EN
topic Selenium nanoparticles
Amantadine
Influenza virus
Apoptosis
Medicine (General)
R5-920
spellingShingle Selenium nanoparticles
Amantadine
Influenza virus
Apoptosis
Medicine (General)
R5-920
Li Y
Lin Z
Guo M
Zhao M
Xia Y
Wang C
Xu T
Zhu B
Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways
description Yinghua Li,* Zhengfang Lin,* Min Guo, Mingqi Zhao, Yu Xia, Changbing Wang, Tiantian Xu, Bing Zhu Center Laboratory, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China *These authors contributed equally to this work Introduction: As a therapeutic antiviral agent, the clinical application of amantadine (AM) is limited by the emergence of drug-resistant viruses. To overcome the drug-resistant viruses and meet the growing demand of clinical diagnosis, the use of biological nanoparticles (NPs) has increased in order to develop novel anti-influenza drugs. The antiviral activity of selenium NPs with low toxicity and excellent activities has attracted increasing attention for biomedical intervention in recent years.Methods and results: In the present study, surface decoration of selenium NPs by AM (Se@AM) was designed to reverse drug resistance caused by influenza virus infection. Se@AM with less toxicity remarkably inhibited the ability of H1N1 influenza to infect host cells through suppression of the neuraminidase activity. Moreover, Se@AM could prevent H1N1 from infecting Madin Darby Canine Kidney cell line and causing cell apoptosis supported by DNA fragmentation and chromatin condensation. Furthermore, Se@AM obviously inhibited the generation of reactive oxygen species and activation of phosphorylation of AKT.Conclusion: These results demonstrate that Se@AM is a potentially efficient antiviral pharmaceutical agent for H1N1 influenza virus. Keywords: selenium nanoparticles, amantadine, influenza virus, apoptosis, nanodrug
format article
author Li Y
Lin Z
Guo M
Zhao M
Xia Y
Wang C
Xu T
Zhu B
author_facet Li Y
Lin Z
Guo M
Zhao M
Xia Y
Wang C
Xu T
Zhu B
author_sort Li Y
title Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways
title_short Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways
title_full Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways
title_fullStr Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways
title_full_unstemmed Inhibition of H1N1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ROS-mediated AKT signaling pathways
title_sort inhibition of h1n1 influenza virus-induced apoptosis by functionalized selenium nanoparticles with amantadine through ros-mediated akt signaling pathways
publisher Dove Medical Press
publishDate 2018
url https://doaj.org/article/6c60bda584094bb5885a5e409d69e074
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