首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Antiviral activity of 1-docosanol an inhibitor of lipid-enveloped viruses including herpes simplex.
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Antiviral activity of 1-docosanol an inhibitor of lipid-enveloped viruses including herpes simplex.

机译:1-二十二烷醇的抗病毒活性这是一种脂质包裹的病毒(包括单纯疱疹)的抑制剂。

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摘要

This article reports that 1-docosanol, a 22-carbon-long saturated alcohol, exerts a substantial inhibitory effect on replication of certain viruses (e.g., herpes simplex virus and respiratory syncytial virus) within primary target cells in vitro. To study the basis for its viral inhibitory activity, a suspension of 1-docosanol was formulated in an inert and nontoxic surfactant, Pluronic F-68; this suspension exerted potent inhibitory activity on the ability of susceptible viruses to infect cultured target cells. Susceptible viruses included wild-type herpes simplex viruses 1 and 2 as well as acyclovir-resistant herpes simplex virus 2 and also respiratory syncytial virus--all of which are lipid-enveloped. In contrast, nonenveloped poliovirus was not susceptible to the inhibitory action of 1-docosanol. Although the precise mechanism has yet to be defined, current evidence suggests that 1-docosanol inhibits viral replication by interfering with the early intracellular events surrounding viral entry into target cells. It is possible that interaction between the highly lipophilic compound and components of target cell membranes renders such target cells less susceptible to viral fusion and/or entry. If this mechanism proves to be correct, 1-docosanol may provide a broad spectrum activity against many different viruses, especially those with lipid-containing envelopes.
机译:本文报道了1-二十二烷醇(一种22碳长的饱和醇)在体外对某些病毒(例如单纯疱疹病毒和呼吸道合胞病毒)的复制具有实质性的抑制作用。为了研究其病毒抑制活性的基础,将1-二十二烷醇的悬浮液配制成惰性无毒的表面活性剂Pluronic F-68;该悬浮液对易感病毒感染培养的靶细胞的能力具有强大的抑制作用。易感病毒包括野生型单纯疱疹病毒1和2以及抗阿昔洛韦的单纯疱疹病毒2以及呼吸道合胞病毒-所有这些都被脂质包裹。相比之下,非包膜脊髓灰质炎病毒对1-二十二烷醇的抑制作用不敏感。尽管尚未确定确切的机制,但目前的证据表明1-二十二烷醇可通过干扰病毒进入靶细胞的早期细胞内事件来抑制病毒复制。高度亲脂性化合物与靶细胞膜成分之间的相互作用可能会使此类靶细胞不易受到病毒融合和/或进入。如果这种机制被证明是正确的,则1-二十二烷醇可以提供针对许多不同病毒的广谱活性,尤其是那些带有脂质包裹物的病毒。

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