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Highly potent anti-HIV-1 activity isolated from fermented Polygonum tinctorium Aiton.

机译:从发酵的何首乌A中分离出的高效抗HIV-1活性。

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A water-soluble extract of fermented Polygonum tinctorium Aiton (Polygonaceae) called Sukumo, exhibited a potent inhibitory activity against HIV type 1 in vitro. The extract potently suppressed acute HIV-1 (III(B)) infection in MT-4 cells with EC(50) values of 0.5mug/ml but exhibited low cytotoxicity to MT-4 cells even at a high concentration (CC(50)>1000mug/ml). It also inhibited giant cell formation in co-cultures of HIV-infected cells and uninfected Molt-4 cells. Sukumo extract was found to interact with both the viral envelope glycoprotein and cellular receptors, thus blocking virus-cell binding and virus-induced syncytium formation. There was a good correlation between the extract's anti-HIV-1 activity and its inhibitory effects on HIV-1 binding. It also suppressed replication of herpes simplex virus type 1 in Vero cells with an EC(50) of 11.56mug/ml. On the other hand, there was no appreciable activity against influenza A virus, poliovirus or SARS corona virus when tested at concentrations ranging from 3.2-400mug/ml as shown by microscopic image analysis for cytopathic effect (CPE). Physico-chemical studies revealed that the anti-HIV activity in the extract was essentially maintained after boiling at 100 degrees C in 1N HCl or 1N NaOH, and after treatment with 100mM NaIO(4). The inhibitory activity of the extract was also not reduced after pronase digestion. The active factor in the extract is likely to be a novel compound(s) having a polyanionic substructure and a molecular weight of 10,000-50,000.
机译:被称为Sukumo的发酵的何首乌(Polygonaceae)的水溶性提取物在体外表现出对1型HIV的有效抑制活性。该提取物可有效抑制MT-4细胞中的急性HIV-1(III(B))感染,其EC(50)值为0.5mug / ml,但即使在高浓度下也对MT-4细胞具有低细胞毒性(CC(50)) > 1000mug / ml)。在HIV感染的细胞和未感染的Molt-4细胞的共培养中,它也抑制了巨细胞的形成。发现Sukumo提取物与病毒包膜糖蛋白和细胞受体都相互作用,从而阻断了病毒与细胞的结合以及病毒诱导的合胞体的形成。提取物的抗HIV-1活性与其对HIV-1结合的抑制作用之间存在良好的相关性。它还以11.56mug / ml的EC(50)抑制了Vero细胞中1型单纯疱疹病毒的复制。另一方面,如显微镜图像分析所显示的细胞病变效应(CPE)所示,当浓度范围为3.2-400μg/ ml时,对甲型流感病毒,脊髓灰质炎病毒或SARS冠状病毒没有明显的活性。物理化学研究表明,提取液中的抗HIV活性在1N HCl或1N NaOH中于100摄氏度煮沸后,以及用100mM NaIO(4)处理后,基本上得以维持。链酶消化后,提取物的抑制活性也没有降低。提取物中的活性因子可能是具有聚阴离子亚结构且分子量为10,000-50,000的新型化合物。

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