1. Academic Validation
  2. Effects and mechanism of Qingke Pingchuan granules against influenza virus infection

Effects and mechanism of Qingke Pingchuan granules against influenza virus infection

  • Arch Virol. 2024 May 28;169(6):130. doi: 10.1007/s00705-024-06053-z.
Linqing He # 1 Jiarui Cao # 1 Xiaolin Xie 1 Yayun Zhang 2 Xue Zhang 2 Hengbin Wang 2 Lingman Ma 3
Affiliations

Affiliations

  • 1 School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Road, Nanjing, Jiangsu Province, 211198, China.
  • 2 Lei Yun Shang Pharmaceutical Group Co., Ltd, Suzhou, 215009, China.
  • 3 School of Life Science and Technology, China Pharmaceutical University, 639 Longmian Road, Nanjing, Jiangsu Province, 211198, China. 1620174416@cpu.edu.cn.
  • # Contributed equally.
Abstract

Qingke Pingchuan granules (QPGs), which contain Houttuynia cordata Thunb, Fritillaria cirrhosa, fired licorice, and fired bitter almonds, among other components, can clear heat and ventilate the lungs, relieving cough and asthma. Clinically, QPGs are mainly used to treat cough, asthma, fever and other discomforts caused by acute or chronic bronchitis. In this study, the Antiviral activity of QPGs against respiratory syncytial virus (RSV), influenza A virus A/FM/1/47 (H1N1), oseltamivir-resistant H1N1, A/Beijing/32/92 (H3N2), Sendai virus, and human adenovirus type 3 in Hep-2 or MDCK cells was evaluated using the CCK-8 method, and the cytotoxicity of QPGs to these two cell lines was tested. The effect of QPGs on mice infected with influenza A virus A/FM/1/47 (H1N1) was evaluated by measuring body weight, survival time, and survival rate, as well as virus titers and lesions in the lungs and levels of inflammatory factors in serum. In addition, the expression of TLR-7-My88-NF-κB signaling pathway-related proteins in lung tissues was analyzed by Western blotting and qRT-PCR. The results showed that QPGs had a potent inhibitory effect on the six viruses tested in vitro. Interestingly, QPGs also displayed particularly pronounced Antiviral activity against H1N1-OC, similar to that of oseltamivir, a well-known Antiviral drug. QPGs effectively protected mice from Infection by H1N1, as indicated by significantly increased body weights, survival times, and survival rates and reduced lung virus titers of inflammatory factors and lung tissue injury. The levels of TLR-7-MyD88-NF-κB-pathway-related proteins in the lung tissue of infected mice were found to be decreased after QPG treatment, thereby alleviating lung injury caused by excessive release of inflammatory factors. Taken together, these findings indicate that QPGs have satisfactory activity against Influenza Virus infection.

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