Antiviral effects of Jinxin oral liquid against respiratory syncytial virus infection in the BALB/c mice model

被引:23
作者
Chen, Zheng-Guang [1 ,2 ]
Luo, Hui [3 ]
Wang, Shou-Chuan [1 ,2 ]
Xu, Jian-Ya [1 ,2 ]
Li, Jia-Xi [4 ]
机构
[1] Nanjing Univ Chinese Med, Inst Pediat, Nanjing 210029, Jiangsu, Peoples R China
[2] Jingsu Key Lab Pediat Resp Dis, Nanjing 210029, Jiangsu, Peoples R China
[3] Childrens Hosp Zhengzhou, Tradit Chinese Med Dept, Zhengzhou 450000, Peoples R China
[4] Shenzhen Childrens Hosp, Tradit Chinese Med Dept, Shenzhen 518000, Peoples R China
基金
中国国家自然科学基金;
关键词
Jinxin oral liquid; Respiratory syncytial virus; TLR3; IRF3; SOCS1; TOLL-LIKE RECEPTOR; HOST-DEFENSE; INTERFERON; ACTIVATION; IRF;
D O I
10.1016/j.jep.2015.01.002
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharrnacological relevance: Jinxin oral liquid (JOL) is used in traditional Chinese medicine (TCM) to treat influenza, cough, asthma, and viral pneumonia, on the basis of Ma Xing Shi Gan Tang (MXSGT) and the clinical experience of Professor Wang Shouchuan, one of the most prestigious pediatricians in China. Aim of study: To investigate the anti-inflammatory and antiviral activities of JUL in mice infected with respiratory syncytial virus (RSV). Materials and methods: Mice were orally administered JUL at doses of 27.6 g kg(-1) d(-1) and 55.2 g kg(-1) d(-1) for 1, 3, or 6 d after RSV challenge. The viral loads in the lung tissue were measured by real-time RT-PCR. The levels of IFN-beta in bronchoalveolar lavage fluid (BLAF) and lung tissue were detected by ELISA and real-time RT-PCR, respectively. The mRNA and protein expression of TLR3, IRF3, and SOCS1 were detected by real-time RT-PCR and western blot, respectively. The protein expression of phoshorylated-IRF3 (p-IRF3) was detected by western blot. Results: JUL significantly ameliorated lung inflammation in RSV-infected mice, and significantly reduced the viral load in the lung tissues. On days 2 and 4 after infection, the mRNA and protein expression of IFN-beta, TLR3, IRF3 (p-IRF3), and SOCS1 were significantly downregulated in RSV-infected mice treated with JUL However, 7 d after infection, JUL significantly upregulated the RSV-induced decrease in IFN-beta, TLR3, and IRF3 (p-IRF3), but reduced SOCS1 expression. Conclusions: JUL ameliorated lung inflammation and inhibited virus replication significantly in RSV-infected mice. During early stage infection, the effect of JUL was improved through inhibition of the TLR3-IRF3-IFN-13 signaling pathway and the expression of SOCS1, whereas during the later stage of infection, JUL upregulated the expression of key signaling molecules in the TLR3 signaling pathway and downregulated the expression of SOCS1. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:287 / 295
页数:9
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