Polygalasaponin F treats mice with pneumonia induced by influenza virus
Autor: | Jin-Yuan Liu, Fang Zhao, Pei-Ping Xu, Yi Ye, Hui-Xian Wang |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Oseltamivir Immunology medicine.disease_cause Virus Mice 03 medical and health sciences chemistry.chemical_compound Influenza A Virus H1N1 Subtype 0302 clinical medicine Orthomyxoviridae Infections Interferon medicine Influenza A virus Animals Pharmacology (medical) Lung Pharmacology Mice Inbred BALB C Respiratory tract infections Signaling pathway business.industry Pneumonia Saponins medicine.disease Triterpenes 030104 developmental biology chemistry Cytokines Original Article Female Tumor necrosis factor alpha Polygalasaponin F Influenza virus business Viral load 030217 neurology & neurosurgery Signal Transduction medicine.drug |
Zdroj: | Inflammopharmacology |
ISSN: | 1568-5608 0925-4692 |
DOI: | 10.1007/s10787-019-00633-1 |
Popis: | Background Influenza is an acute viral respiratory illness that causes high morbidity and mortality globally. Therapeutic actions are limited to vaccines and a few anti-viral drugs. Polygala (P.) japonica herba is rich in Polygalasaponin F (PSF, C53H86O23), used for acute bronchitis, pharyngitis, pneumonia, amygdalitis, and respiratory tract infections treatment in China. Hypercytokinemia is often correlated with severe pneumonia caused by several influenza viruses. PSF was reported to have anti-inflammatory effects and its mechanism is associated with the nuclear factor (NF)-κB signaling pathway. The action of PSF to alleviate pulmonary inflammation caused by influenza A virus (IAV) infection requires careful assessment. In the present study, we evaluated the effect and mechanism of PSF on mice with pneumonia caused by influenza H1N1 (A/FM/1/47). Methods Mice were infected intranasally with fifteen 50% mouse lethal challenge doses (MLD50) of influenza virus. BALB/c mice were treated with PSF or oseltamivir (oral administration) for 2 h post-infection and received concomitant treatment for 5 days after infection. On day 6 post-infection, 10 mice per group were killed to collect related samples, measure body weight and lung wet weight, and detect the viral load, cytokine, prostaglandins, pathological changes, and cell pathway protein expression in the lungs. In addition, the survival experiments were carried out to investigate the survival of mice. The expression profile of cell pathway proteins was detected and analyzed using a broad pathway antibody array and confirmed the findings from the array by western blotting. Results Polygalasaponin F and oseltamivir can protect against influenza viral infection in mice. PSF and oseltamivir significantly relieved the signs and symptoms, reduced body weight loss, and improved the survival rate of H1N1-infected mice. Moreover, PSF efficiently decreased the level of interleukin (IL)-1β, tumor necrosis factor (TNF)-α, IL-4, interferon (IFN)-γ, thromboxane A2 (TXA2), and prostaglandin E2 (PGE2) in lung tissues of mice infected with influenza virus (p |
Databáze: | OpenAIRE |
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