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Preliminary study of Yinhuapinggan granule against H1N1 influenza virus infection in mice through inhibition of apoptosis. | LitMetric

AI Article Synopsis

  • YHPG is a traditional Chinese medicine used to treat fever, cough, and viral pneumonia, and this study aims to explore its antiviral effects against H1N1 influenza virus in mice.
  • YHPG showed a dose-dependent reduction in lung index and viral load in infected mice, with higher doses leading to improved lung health and increased immune tissue sizes.
  • The mechanism appears to involve regulating apoptosis by reducing levels of Bax and caspase-3 and increasing Bcl-2 expression, suggesting that YHPG could be a potential antiviral treatment for influenza.

Article Abstract

Context: Yinhuapinggan granule (YHPG) is frequently used for treating fever, cough, and viral pneumonia in traditional Chinese medicine.

Objective: This study investigated the antiviral effects of YHPG in H1N1 influenza virus (IFV)-infected mice and its possible mechanism.

Materials And Methods: ICR mice were intranasally infected with 10 LD viral dose of IFV and then oral administration of YHPG (6, 12, and 18 g/kg) or oseltamivir (positive control) once a day for 2 or 4 consecutive days, six mice in each group. The lung, spleen and thymus indexes of IFV-infected mice, the expression of viral loads and pathological changes in lung tissues were performed to evaluate the antiviral effects of YHPG. Real-time PCR, immunohistochemistry and western blot assays were used to determine the expression of Bax, Bcl-2 and caspase-3.

Results: LD in mice was 10/0.02 mL. YHPG (6, 12, and 18 g/kg) dose-dependently decreased the lung index and viral load; the inhibition ratio of lung index was 5.31, 18.22, and 34.06%, respectively. Further detection revealed that YHPG (12 and 18 g/kg) significantly attenuated lung pathological changes, and increased the spleen and thymus indexes. Moreover, YHPG significantly down-regulated the mRNA and protein expression of Bax and caspase-3 in lung tissues of mice infected with IFV, and up-regulated the expression of Bcl-2.

Conclusions: YHPG has significant antiviral effects in IFV-infected mice, partially by inhibiting influenza virus replication and regulating the occurrence of apoptosis induced by influenza virus infection, suggesting that YHPG may be a promising antiviral agent with potential clinical application prospects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534346PMC
http://dx.doi.org/10.1080/13880209.2020.1818792DOI Listing

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