Anti-influenza virus effects of crude phenylethanoid glycosides isolated from ligustrum purpurascens via inducing endogenous interferon-γ
Anti-influenza virus effects of crude phenylethanoid glycosides isolated from ligustrum purpurascens via inducing endogenous interferon-γ
复制标题
从女贞中分离的粗苯乙醇苷通过诱导内源性干扰素-γ的抗流感病毒作用。
DOI:
10.1016/j.jep.2015.07.019
复制
发表时间:
2016-02-17
影响因子:
5.4
通讯作者:
He, Zhen-dan
中科院分区:
文献类型:
--
作者:
Hu, Xiao-peng;Shao, Min-ming;He, Zhen-dan
Ethnopharmacological relevance: Ligustrum purpurascens Y.C. Yang (Oleaceae) is traditionally recorded as "Ku Ding Cha", a kind of functional tea in southern China for about two thousand years, which has been reported with sore throat alleviating and pathogenic heat expelling effects. However, there are no scientific studies demonstrating its antiviral activity. The aim of the study: This study is aimed at investigating the anti-influenza virus effects of phenylethanoid glycosides isolated from L. purpurascens (LPG) as well as its corresponding mechanisms.Materials and methods: In vitro, hemagglutination assay was employed to detect the influenza virus titer; In vivo, C57BL/6J mice were given oral administration of LPG (100 mg/kg, 300 mg/kg, 900 mg/kg) or ribavirin (100 mg/kg) once daily for 5 successive days. Meanwhile, on the second day, mice were infected intranasally (i.n.) with A/FM/1/47 H1N1 virus. Mice survival rate and other clinical index were monitored for 15 days. Infected mice were sacrificed to measure the lung lesion and stained with hematoxylineosin. Flow cytometry analyses spleen lymphocytes and interferon-gamma (IFN-gamma) level. The IFN-gamma knockout mice (IFN-gamma(-/-) mice, C57BL/6J) which had been verified lacking IFN-gamma through Western Blot, were applied in the death-protection test to identify the role of IFN-gamma played in LPG antiviral effect.Results: In vitro, LPG at 0.5 mg/ml inhibited Influenza A Virus H1N1 type (H1N1) infection of MDCK cells. In vivo, LPG at 300 and 900 mg/kg significantly decreased the mouse lung index (p < 0.05), alleviated influenza-induced lethality and clinical symptoms, and therefore enhanced mouse survival (p