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10.1016/j.phrs.2020.104850

http://scihub22266oqcxt.onion/10.1016/j.phrs.2020.104850
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32360580!7192119!32360580
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suck abstract from ncbi


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pmid32360580      Pharmacol+Res 2020 ; 158 (ä): 104850
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  • Liu Shen capsule shows antiviral and anti-inflammatory abilities against novel coronavirus SARS-CoV-2 via suppression of NF-kappaB signaling pathway #MMPMID32360580
  • Ma Q; Pan W; Li R; Liu B; Li C; Xie Y; Wang Z; Zhao J; Jiang H; Huang J; Shi Y; Dai J; Zheng K; Li X; Yang Z
  • Pharmacol Res 2020[Aug]; 158 (ä): 104850 PMID32360580show ga
  • 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-alpha, IL-6, IL-1beta, 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-kappaB/MAPK signaling pathway was detected by western blot and it was found that LS could inhibit the expression of p-NF-kappaB p65, p-IkappaBalpha and p-p38 MAPK, while increasing the expression of IkappaBalpha. 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-kappaB/MAPK signaling pathway in vitro, making its promising candidate treatment for controlling COVID-19 disease.
  • |Adenosine Monophosphate/analogs & derivatives/pharmacology[MESH]
  • |Alanine/analogs & derivatives/pharmacology[MESH]
  • |Animals[MESH]
  • |Anti-Inflammatory Agents/pharmacology[MESH]
  • |Antiviral Agents/pharmacology[MESH]
  • |Betacoronavirus/*drug effects[MESH]
  • |COVID-19[MESH]
  • |Cell Proliferation/drug effects[MESH]
  • |Cells, Cultured[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Complex Mixtures/*pharmacology[MESH]
  • |Coronavirus Infections/virology[MESH]
  • |Humans[MESH]
  • |Inflammation Mediators/metabolism[MESH]
  • |NF-kappa B/*antagonists & inhibitors/*metabolism[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/virology[MESH]
  • |SARS-CoV-2[MESH]
  • |Signal Transduction/*drug effects[MESH]


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