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黄芩根中植物黄酮5,7,4'-三羟基-8-甲氧基黄酮对甲型(H3N2)和乙型流感病毒的抗病毒活性

Antiviral activity of plant flavonoid, 5,7,4'-trihydroxy-8-methoxyflavone, from the roots of Scutellaria baicalensis against influenza A (H3N2) and B viruses.

作者信息

Nagai T, Suzuki Y, Tomimori T, Yamada H

机构信息

Oriental Medicine Research Center, Kitasato Institute, Tokyo, Japan.

出版信息

Biol Pharm Bull. 1995 Feb;18(2):295-9. doi: 10.1248/bpb.18.295.

Abstract

We investigated effects of isoscutellarein-8-methylether (5,7,4'-trihydroxy-8-methoxyflavone, F36) from the roots of Scutellaria baicalensis on the single-cycle replication of mouse-adapted influenza viruses A/Guizhou/54/89 (H3N2 subtype) and B/Ibaraki/2/85 in Madin-Darby canine kidney (MDCK) cells. The agent suppressed replication of these viruses from 6 to 12 h after incubation in a dose-dependent manner by 50% at 20 microM and 90% at 40 microM, respectively. F36 (50 microM) reduced the release of B/Ibaraki virus in the medium by 90-93% when it was added to the MDCK cells at 0 to 4 h after incubation. The cell-associated virus determined by sialidase activity was also reduced by the treatment at 0 to 4 h. F36 (120 microM) inhibited the low pH-dependent membrane fusion of both the viruses with the liposome containing mixed gangliosides from bovine brain. However, the agent little affected the hemagglutination and RNA-dependent RNA polymerase activities of these viruses in vitro. These results suggest that F36 inhibits the replication of A/Guizhou and B/Ibaraki viruses at least partly by inhibiting the fusion of viral envelopes with the endosome/lysosome membrane which occurs at the early stage of the virus infection cycle. F36 (0.5 mg/kg) showed no antiviral activity against A/Guizhou and B/Ibaraki viruses in mice when administered intranasally 5 min prior to virus inoculation, whereas it significantly inhibited their proliferation in the mouse lung when administered intranasally 7 times (total 3.5 mg/kg) from 18 h before to 54 h after virus infection.

摘要

我们研究了从黄芩根中提取的异黄芩素-8-甲醚(5,7,4'-三羟基-8-甲氧基黄酮,F36)对适应小鼠的甲型流感病毒A/贵州/54/89(H3N2亚型)和乙型流感病毒B/茨城县/2/85在犬肾传代细胞(MDCK)中单次循环复制的影响。该药物在孵育6至12小时后以剂量依赖性方式抑制这些病毒的复制,在20微摩尔时抑制50%,在40微摩尔时抑制90%。当在孵育后0至4小时将F36(50微摩尔)添加到MDCK细胞中时,其可使培养基中B/茨城县病毒的释放减少90%至93%。在0至4小时进行处理也可减少通过唾液酸酶活性测定的细胞相关病毒。F36(120微摩尔)抑制了这两种病毒与含有来自牛脑的混合神经节苷脂的脂质体的低pH依赖性膜融合。然而,该药物在体外对这些病毒的血凝和RNA依赖性RNA聚合酶活性影响很小。这些结果表明,F36至少部分通过抑制病毒包膜与在病毒感染周期早期发生的内体/溶酶体膜的融合来抑制A/贵州和B/茨城县病毒的复制。当在病毒接种前5分钟经鼻给药时,F36(0.5毫克/千克)对小鼠体内的A/贵州和B/茨城县病毒没有抗病毒活性,而当在病毒感染前18小时至感染后54小时经鼻给药7次(总量3.5毫克/千克)时,它可显著抑制它们在小鼠肺中的增殖。

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