Antiviral Effect of Cimicifugin from Cimicifuga foetida Against Human Respiratory Syncytial Virus

被引:3
作者
Wang, Kuo-Chih [1 ]
Chang, Jung-San [2 ,4 ]
Lin, Liang-Tzung [5 ]
Chiang, Lien-Chai [3 ]
Lin, Chun-Ching [1 ]
机构
[1] Kaohsiung Med Univ, Coll Pharm, Sch Pharm, Grad Inst Nat Prod, Kaohsiung 80708, Taiwan
[2] Kaohsiung Med Univ, Sch Med, Coll Med, Dept Renal Care, Kaohsiung 80708, Taiwan
[3] Kaohsiung Med Univ, Sch Med, Coll Med, Dept Microbiol, Kaohsiung 80708, Taiwan
[4] Kaohsiung Med Univ Hosp, Dept Internal Med, Div Gastroenterol, Kaohsiung 80708, Taiwan
[5] IWK Hlth Ctr, Dept Pediat, Halifax, NS B3K 6R8, Canada
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2012年 / 40卷 / 05期
关键词
Cimicifugin; Respiratory Syncytial Virus (RSV); Antiviral; Viral Attachment; Viral Internalization; Interferon-beta; TUMOR-NECROSIS-FACTOR; NEUTRALIZING ANTIBODY; FUSION GLYCOPROTEIN; PREVENTION; INFECTION; ALPHA;
D O I
10.1142/S0192415X12500760
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Human respiratory syncytial virus (RSV) causes serious infection of the lower respiratory tract in children and an effective antiviral therapy against the viral pathogen remains unavailable. We previously demonstrated that the oriental medicinal plant, Cimicifuga foetida L. (C. foetida), possessed inhibitory activity against RSV. Since cimicifugin is a major constituent of C. foetida, we sought to examine in this study its anti-RSV effect on both the human upper (HEp-2) and lower (A549) respiratory tract cell lines. Results revealed that cimicifugin dose-dependently inhibited RSV-induced plaque formation in both HEp-2 and A549 cells (p < 0.0001), with a superior effect in the latter cell type (p < 0.0001). The antiviral activity of cimicifugin was time-dependent (p < 0.0001) and was most effective when cells were treated with the compound before viral inoculation. Additional experiments demonstrated that cimicifugin could inhibit viral attachment (p < 0.0001) and viral internalization (p < 0.0001). Furthermore, the drug could potentiate heparin's effect against attachment of RSV, particularly in A549 cells. Enzyme-linked immunosorbent assay (ELISA) analysis of antiviral cytokines induction revealed that cimicifugin could also stimulate epithelial cells to secrete IFN-beta to counteract viral infection. Taken together, these results indicate that cimicifugin is an efficient antiviral agent against RSV infection. We suggest that cimicifugin might be useful for the management of RSV pathogenesis.
引用
收藏
页码:1033 / 1045
页数:13
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