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The therapeutic effects of sodium cromoglycate against influenza A virus H5N1 in mice

OBJECTIVES: To identify the protective role of sodium cromoglycate in mice during influenza virus infection. DESIGN: H5N1 virus‐infected mice were treated with the mast cell stabilizer sodium cromoglycate (SCG) to investigate its therapeutic effect. SAMPLE: The nose, trachea and lungs from mice were...

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Detalles Bibliográficos
Autores principales: Han, Deping, Wei, Tangting, Zhang, Siyi, Wang, Ming, Tian, Haiyan, Cheng, Jinlong, Xiao, Jin, Hu, Yanxin, Chen, Mingyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687497/
https://www.ncbi.nlm.nih.gov/pubmed/26176755
http://dx.doi.org/10.1111/irv.12334
Descripción
Sumario:OBJECTIVES: To identify the protective role of sodium cromoglycate in mice during influenza virus infection. DESIGN: H5N1 virus‐infected mice were treated with the mast cell stabilizer sodium cromoglycate (SCG) to investigate its therapeutic effect. SAMPLE: The nose, trachea and lungs from mice were collected. MAIN OUTCOME MEASURES: Virus replication and host responses were determined by plaque assay, quantitative PCR, immunohistochemistry, and histology. RESULTS: SCG‐treated mice survived better than did PBS‐treated mice after H5N1 virus infection. Mild pathological changes with fewer inflammatory cell infiltration and fewer virus antigens were observed in the nose, trachea, and lungs of SCG‐treated mice on days 3 and 5 post‐infection. However, no significant changes in viral load in the lungs were detected between SCG‐ and PBS‐treated mice. Furthermore, significantly decreased expression of interleukin‐6, tumor necrosis factor‐a, Toll‐like receptor 3, and TIR‐domain‐containing adapter‐inducing interferon‐b was detected in the lungs of SCG‐treated mice, and no higher expression of interferon‐c was detected. CONCLUSION: These results suggest that SCG has therapeutic roles in H5N1 virus‐infected mice by alleviating the inflammatory response rather than inhibition of viral replication in the lungs.