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首页> 外文期刊>International journal of molecular medicine >Antiviral activity of Isatis indigotica root-derived clemastanin?B against human and avian influenza A and B viruses in vitro
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Antiviral activity of Isatis indigotica root-derived clemastanin?B against human and avian influenza A and B viruses in vitro

机译:板蓝根来源的clemastanin?B对人和禽流感A和B病毒的体外抗病毒活性

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摘要

Clemastanin?B, 7S,8R,8'R-(-)-lariciresinol-4,4'-bis-O-β-D-glucopyranoside, is one of the major lignans extracted from Isatis indigotica root (IIR). In this study, the anti-influenza activities of clemastanin?B were evaluated in?vitro. Clemastanin?B was found to inhibit different subtypes of human (H1N1, including swine-origin H1N1; H3N2 and influenza?B) and avian influenza viruses (H6N2, H7N3, H9N2) at different magnitudes of activity (IC50 0.087-0.72?mg/ml) while this compound was inactive against respiratory syncytial virus (RSV), adenovirus?3 (ADV3), parainfluenza virus?3 (PIV3), enterovirus?71 (EV71) and human rhinovirus (HRV). An apparent virus titer reduction was detected when MDCK cells were treated with clemastanin?B after viral infection, particularly at the early stage, and the ribonucleoprotein (RNP) of the influenza virus was retained in the nucleus after treatment with clemastanin?B. These results demonstrated that clemastanin?B targets viral endocytosis, uncoating or RNP export from the nucleus. Furthermore, treatment with clemastanin?B did not easily result in the emergence of viral drug resistance. The effects of clemastanin?B demonstrated in this study may promote the antiviral study of IIR, but additional studies are required to define the anti-influenza mechanism(s).
机译:Clemastanin?B,7S,8R,8'R-(-)-lariciresinol-4,4'-bis-O-β-D-吡喃葡萄糖苷是从板蓝根中提取的主要木脂素之一。在这项研究中,体外评估了clemastanin?B的抗流感活性。发现Clemastanin?B可以以不同的活性水平抑制人的不同亚型(H1N1,包括猪源性H1N1,H3N2和流感B)和禽流感病毒(H6N2,H7N3,H9N2)(IC50为0.087-0.72?mg /该化合物对呼吸道合胞病毒(RSV),腺病毒3(ADV3),副流感病毒3(PIV3),肠病毒71(EV71)和人鼻病毒(HRV)没有活性。当病毒感染后,尤其是在早期,用clemastanin?B处理MDCK细胞时,发现病毒滴度明显降低,并且用clemastanin?B处理后,流感病毒的核糖核蛋白(RNP)保留在细胞核中。这些结果表明,clemastanin?B靶向病毒内吞,脱壳或RNP从细胞核输出。此外,使用clemastanin?B的治疗不容易导致病毒耐药性的出现。本研究中证实的clemastanin?B的作用可能会促进IIR的抗病毒研究,但还需要进行其他研究来确定抗流感机制。

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