首页|紫草素(shikonin)抗奥密克戎毒株的实验研究及机制分析

紫草素(shikonin)抗奥密克戎毒株的实验研究及机制分析

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目的 探讨右旋体紫草素(shikonin)抗奥密克戎毒株的药理作用和对新型冠状病毒主蛋白酶的抑制活性。方法 使用奥密克戎毒株BA。2。2转染的Vero细胞模型检测shikonin的抗病毒活性;利用体外主蛋白酶荧光偏振模型测试shikonin对于新型冠状病毒主蛋白酶的抑制活性,实验以奈玛特韦为阳性对照化合物。结果 Vero细胞模型药理活性测试发现shikonin具有抑制奥密克戎毒株核酸复制的作用;而在体外荧光偏振模型活性测试实验中,shikonin在20、50 μM药物浓度并未表现出对主蛋白酶的显著抑制活性。结论 紫草素(shikonin)在细胞水平的实验中表现出抗奥密克戎毒株的药理活性,但其可能是主蛋白酶的非特异性抑制剂,抗病毒的作用机理极可能为抑制新型冠状病毒RNA聚合酶。
Preliminary study on Activity of Shikonin against Omicron Subvariant and Mechanism Analysis
Objective To investigate the pharmacological activity of shikonin against Omicron strain and the inhibitory effect on the main protease of the novel coronavirus.Methods The antiviral activity of shikonin was tested using the Vero cell model trans-fected with the omicron BA.2.2 strain,and then nirmatrelvir was used as a positive control compound,and the inhibitory activity of shikonin against the novel coronavirus main protease was tested by using main protease fluorescence polarisation screening model in vitro.Results The extracorporal pharmacological activity test used Vero cell model showed that shikonin had the effect of inhibiting nucleic acid replication of the omicron strain,but shikonin did not show significant inhibitory activity against the main protease at the 20μM、50μM concentrations in a fluorescence polarisation screening model activity test.Conclusion Shikonin has pharmacological activity against the omicron strain at the cellular level,but it may be a non-specific inhibitor of the main prote-ase,and the mechanism of antiviral action is most likely to inhibit the novel coronavirus RNA polymerase.

shikoninOmicron SubvariantRNA polymerasemain proteasefluorescence polarisation screening modelmolec-ular dock

王秀民、谢小华、孙永、袁媛、崔志梅、张涛、苏彦雷、孙殿兴、吴红海、张晶

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石家庄市中医院,河北石家庄 050011

河北省人民医院,河北石家庄 050051

安徽省疾病预防控制中心,安徽合肥 230601

联勤保障部队第九八○医院,河北石家庄 050082

中国医学科学院、北京协和医学院医药生物技术研究所,北京 100050

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紫草素 奥密克戎毒株 RNA聚合酶 主蛋白酶 荧光偏振筛选模型 分子对接

2024

中华中医药学刊
中华中医药学会 ,辽宁中医药大学

中华中医药学刊

CSTPCD北大核心
影响因子:1.007
ISSN:1673-7717
年,卷(期):2024.42(9)