首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >The Effectiveness and Mechanism ofToona sinensisExtract Inhibit Attachment of Pandemic Influenza A (H1N1) Virus
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The Effectiveness and Mechanism ofToona sinensisExtract Inhibit Attachment of Pandemic Influenza A (H1N1) Virus

机译:香椿提取物抑制大流行性甲型流感病毒(H1N1)的附着作用及其机制

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TSL-1 is a fraction of the aqueous extract from the tender leaf ofToona sinensis Roem, a nutritious vegetable. The pandemic influenza A (H1N1) virus is a recently described, rapidly contagious respiratory pathogen which can cause acute respiratory distress syndrome (ARDS) and poses a major public health threat. In this study, we found that TSL-1 inhibited viral yields on MDCK plaque formation by pandemic influenza A (H1N1) virus on infected A549 cells with high selectivity index. Meanwhile, TSL-1 also suppressed viral genome loads in infected A549 cells, quantified by qRT-PCR. This study further demonstrated that TSL-1 inhibited pandemic influenza A (H1N1) virus activity through preventing attachment of A549 cells but not penetration. TSL-1 inhibited viral attachment through significant downregulation of adhesion molecules and chemokines (VCAM-1, ICAM-1, E-selectin, IL-8, and fractalkine) compared to Amantadine. Our results suggest that TSL-1 may be used as an alternative treatment and prophylaxis against pandemic influenza A (H1N1) virus.
机译:TSL-1是营养植物香椿的嫩叶中水提取物的一部分。大流行性甲型流感(H1N1)病毒是最近描述的一种具有快速传染性的呼吸道病原体,可引起急性呼吸窘迫综合征(ARDS),并构成主要的公共健康威胁。在这项研究中,我们发现TSL-1在高选择性指数感染的A549细胞上抑制了大流行性流感A(H1N1)病毒对MDCK斑块形成的病毒产量。同时,TSL-1还抑制了被感染的A549细胞中的病毒基因组负荷,通过qRT-PCR定量。这项研究进一步证明,TSL-1通过阻止A549细胞附着而不是穿透来抑制大流行性甲型流感病毒(H1N1)的活性。与金刚烷胺相比,TSL-1通过显着下调粘附分子和趋化因子(VCAM-1,ICAM-1,E-选择素,IL-8和fractalkine)抑制病毒附着。我们的结果表明,TSL-1可用作替代治疗和预防大流行性甲型流感(H1N1)病毒。

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