Exploring antiviral effect and mechanism of Jinye Baidu granules(JYBD) against influenza A virus through network pharmacology and in vitro and in vivo experiments

被引:0
作者
Chen, Zhixuan [1 ,2 ,3 ]
Mo, Qinxian [1 ,2 ,3 ,4 ]
Luo, Siqi [1 ,2 ,3 ]
Liang, Jinlong [1 ,2 ,3 ]
Li, Yinyan [1 ,2 ,3 ]
Gao, Yinhuang [1 ,2 ,3 ]
Zhang, Chunyu [1 ,2 ,3 ]
Jiang, Linrui [1 ,2 ,3 ]
Ma, Jun [4 ]
Yang, Sizu [1 ,2 ,3 ]
Jiang, Feng [1 ,2 ,3 ]
Liu, Menghua [1 ,2 ,3 ]
Liu, Shuwen [1 ,2 ,3 ]
Yang, Jie [1 ,2 ,3 ]
机构
[1] Southern Med Univ, NMPA Key Lab Res & Evaluat Drug Metab, Sch Pharmaceut Sci, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Screening, Guangzhou 510515, Peoples R China
[3] Southern Med Univ, Sch Pharmaceut Sci, Guangdong Hongkong Macao Joint Lab New Drug Screen, Guangzhou 510515, Guangdong, Peoples R China
[4] Sinopharm Zhonglian Pharmaceut Co Ltd, Wuhan 430000, Peoples R China
关键词
Influenza A virus; Jinye Baidu granules; Chemical profile; Potential mechanism; Inflammatory response; ACTIVATED PROTEIN-KINASE; INHIBITION; EXPRESSION; RESISTANCE; MICE;
D O I
10.1016/j.jep.2024.118720
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Jinye Baidu granules (JYBD) have been used to treat acute respiratory tract infections and demonstrated clinical efficacy for the treatment of emerging or epidemic respiratory viruses such as SARS-CoV-2 and influenza virus. Aim of the study: This study is to investigate the antiviral effect of JYBD against influenza A viruses (IAV) in vitro and in vivo and elucidate its underlying mechanism. Materials and methods: Ultra-high-performance liquid chromatography connected with Orbitrap mass spectrometer (UHPLC-Orbitrap MS) was employed to describe the chemical profile of JYBD. The potential pathways and targets involved in JYBD against IAV infection were predicted by network pharmacology. The efficacy and mechanism of JYBD were validated through both in vivo and in vitro experiments. Moreover, combination therapy with JYBD and the classic anti-influenza drugs was also investigated. Results: A total of 126 compounds were identified by UHPLC-Orbitrap MS, of which 9 compounds were unambiguously confirmed with reference standards. JYBD could significantly inhibit the replication of multiple strains of IAV, especially oseltamivir-resistant strains. The results of qRT-PCR and WB demonstrated that JYBD could inhibit the excessive induction of pro-inflammatory cytokines induced by IAV infection and regulate inflammatory response through inhibiting JAK/STAT, NF-kappa B and MAPK pathways. Moreover, both JYBD monotherapy or in combination with oseltamivir could alleviate IAV-induced severe lung injury in mice. Conclusions: JYBD could inhibit IAV replication and mitigate virus-induced excessive inflammatory response. Combinations of JYBD and neuraminidase inhibitors conferred synergistic suppression of IAV both in vitro and in vivo. It might provide a scientific basis for clinical applications of JYBD against influenza virus infected diseases.
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页数:16
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