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About:
Liu Shen capsule shows antiviral and anti-inflammatory abilities against novel coronavirus SARS-CoV-2 via suppression of NF-κB signaling pathway
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Liu Shen capsule shows antiviral and anti-inflammatory abilities against novel coronavirus SARS-CoV-2 via suppression of NF-κB signaling pathway
Creator
Liu, Bin
Li, Xiaobo
Xie, C
Pan, Weiqi
Li, Chufang
Zhao, Jin
Yang, Zifeng
Jiang, Haiming
Li, Runfeng
Huang, Jicheng
Shi, Yongxia
Zheng, Kui
Dai, Jun
Li, Liu
Li, Ma
Liu D #, Bin
Ma, Qinhai
Shen, Liu
Shi, Huang
Wang, Zhoulang
Xie, Yuqi
Source
Elsevier; Medline; PMC; WHO
abstract
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has spread worldwide through person-to-person contact, causing a public health emergency of international concern. At present, there is no specific antiviral treatment recommended for SARS-CoV-2 infection. Liu Shen capsule (LS), a traditional Chinese medicine, has been proven to have a wide spectrum of pharmacological properties, such as anti-inflammatory, antiviral and immunomodulatory activities. However, little is known about the antiviral effect of LS against SARS-CoV-2. Herein, the study was designed to investigate the antiviral activity of SARS-CoV-2 and its potential effect in regulating the host’s immune response. The inhibitory effect of LS against SARS-CoV-2 replication in Vero E6 cells was evaluated by using the cytopathic effect (CPE) and plaque reduction assay. The number of virions of SARS-CoV-2 was observed under transmission electron microscope after treatment with LS. Proinflammatory cytokine expression levels upon SARS-CoV-2 infection in Huh-7 cells were measured by real-time quantitative PCR assays. The results showed that LS could significantly inhibit SARS-CoV-2 replication in Vero E6 cells, and reduce the number of virus particles and it could markedly reduce pro-inflammatory cytokines (TNF-α, IL-6, IL-1β, IL-8, CCL-2/MCP-1 and CXCL-10/IP-10) production at the mRNA levels. Moreover, the expression of the key proteins in the NF-κB/MAPK signaling pathway was detected by western blot and it was found that LS could inhibit the expression of p-NF-κB p65, p-IκBα and p-p38 MAPK, while increasing the expression of IκBα. These findings indicate that LS could inhibit SARS-CoV-2 virus infection via downregulating the expression of inflammatory cytokines induced virus and regulating the activity of NF-κB/MAPK signaling pathway in vitro, making its promising candidate treatment for controlling COVID-19 disease.
has issue date
2020-04-30
(
xsd:dateTime
)
bibo:doi
10.1016/j.phrs.2020.104850
bibo:pmid
32360580
has license
no-cc
sha1sum (hex)
69382cbac0bbdd2437414b92b122815b44d4cf46
schema:url
https://doi.org/10.1016/j.phrs.2020.104850
resource representing a document's title
Liu Shen capsule shows antiviral and anti-inflammatory abilities against novel coronavirus SARS-CoV-2 via suppression of NF-κB signaling pathway
has PubMed Central identifier
PMC7192119
has PubMed identifier
32360580
schema:publication
Pharmacol Res
resource representing a document's body
covid:69382cbac0bbdd2437414b92b122815b44d4cf46#body_text
is
schema:about
of
named entity 'anti-inflammatory'
named entity 'NF-κB'
named entity 'anti-inflammatory'
named entity 'signaling pathway'
named entity 'Liu'
named entity 'antiviral'
named entity 'NF-B'
named entity 'signaling pathway'
named entity 'SARS-CoV-2'
named entity 'coronavirus'
named entity 'TEM'
named entity 'virus'
named entity 'antiviral'
named entity 'antiviral treatment'
named entity 'Suzhou'
named entity 'Vero E6'
named entity 'virus entry'
named entity 'Dulbecco's modified Eagle's medium'
named entity 'TCID50'
named entity 'inflammation'
named entity 'IL-6'
named entity 'virus'
named entity 'ICU'
named entity 'antiviral activity'
named entity 'pro-inflammatory'
named entity 'cell death'
named entity 'SARS-CoV-2'
named entity 'Coronaviruses'
named entity 'Huh-7'
named entity 'aetiology'
named entity 'NF-κB'
named entity 'infection'
named entity 'IFN-γ'
named entity 'Thermo Fisher'
named entity 'transcription factor'
named entity 'p38 MAPK'
named entity 'CCL-2'
named entity 'anserine'
named entity 'MERS-CoV'
named entity 'antiviral'
named entity 'ICU'
named entity 'IκBα'
named entity 'coronaviruses'
named entity 'infection'
named entity 'Vero E6'
named entity 'Vero E6'
named entity 'virus'
named entity 'Wuhan'
named entity 'MAPK signaling pathway'
named entity 'SARS-CoV-2'
named entity 'SARS-CoV-2'
named entity 'immune response'
named entity 'PBS'
named entity 'cytokines'
named entity 'significant difference'
named entity 'IFN-γ'
named entity 'Vero E6'
named entity 'viruses'
named entity 'infection'
named entity 'viruses'
named entity 'pneumonia'
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