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甘草酸对水痘-带状疱疹病毒的体外抗病毒活性。

Antiviral activity of glycyrrhizin against varicella-zoster virus in vitro.

作者信息

Baba M, Shigeta S

出版信息

Antiviral Res. 1987 Feb;7(2):99-107. doi: 10.1016/0166-3542(87)90025-8.

Abstract

One of the plant extracts, glycyrrhizin (GL) was investigated for its antiviral action on varicella-zoster virus (VZV) in vitro. When human embryonic fibroblast (HEF) cells were treated with GL after inoculation of virus (post-treatment), the average 50%-inhibitory dose (ID50) for five VZV strains was 0.71 mM, and the selectivity index (ratio of ID50 for host-cell DNA synthesis to ID50 for VZV replication) was 30. GL was also effective against VZV replication when HEF cells were treated 24 h before the inoculation (pretreatment). Furthermore, at a concentration of 2.4 mM GL inactivated more than 99% of virus particles within 30 min at 37 degrees C. In combination with other anti-herpes drugs (acyclovir, adenine arabinoside, bromovinyldeoxyuridine, and phosphonoformate) or human native beta-interferon, GL had an additive or slightly synergistic effect on VZV replication. The mechanism of anti-VZV action is still unclear. We postulate that GL inhibits the penetration, uncoating or release of virus particles.

摘要

研究了一种植物提取物甘草甜素(GL)在体外对水痘-带状疱疹病毒(VZV)的抗病毒作用。当在接种病毒后(治疗后)用GL处理人胚成纤维细胞(HEF)时,五种VZV毒株的平均50%抑制剂量(ID50)为0.71 mM,选择性指数(宿主细胞DNA合成的ID50与VZV复制的ID50之比)为30。当在接种前24小时(预处理)用GL处理HEF细胞时,GL对VZV复制也有效。此外,在37℃下,2.4 mM的GL浓度在30分钟内可使99%以上的病毒颗粒失活。与其他抗疱疹药物(阿昔洛韦、阿糖腺苷、溴乙烯脱氧尿苷和膦甲酸)或人天然β-干扰素联合使用时,GL对VZV复制具有相加或轻微协同作用。抗VZV作用的机制仍不清楚。我们推测GL抑制病毒颗粒的穿透、脱壳或释放。

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