解表清里方干预甲型H1N1流行性感冒小鼠的抗病毒作用机制
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

国家重点研发计划“中医药现代化”重点专项(2022YFC3500800);中国中医科学院流感防治技术体系(ZZ13-025-06)


Mechanism of Antiviral Action of Jiebiao Qingli Fang in Mice with Influenza A(H1N1)
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    目的:探讨解表清里方对甲型H1N1流行性感冒小鼠的抗病毒作用机制。方法:用随机数字法将36只7周龄雌性BalB/c小鼠随机分为空白组、模型组、西药组及解表清里方高剂量组、中剂量组、低剂量组,每组6只。空白组给予等量生理盐水滴鼻,其余组小鼠给予甲型流感病毒液于左侧鼻孔滴鼻,每只50 μL。造模2 h后,西药组给予0.037 5 g/(kg·d)磷酸奥司他韦灌胃;解表清里方高剂量组、中剂量组、低剂量组分别给予6.05 g/(kg·d)、3.02 g/(kg·d)、1.51 g/(kg·d)解表清里方灌胃。空白组及模型组同时给予生理盐水0.2 mL灌胃,均1次/d,连续5 d。对比各组肺指数、胸腺指数和脾脏指数,肺组织病理变化,肺组织中乳动物雷帕霉素靶蛋白(mTOR)表达,肺悬液中病毒基因及磷脂酰肌醇3激酶(PI3K)、蛋白激酶B(AKT)、糖原合酶激酶3β(GSK-3β)mRNA表达,肺组织中PI3K、AKT、GSK-3β蛋白表达。结果:动物实验结果显示,与模型组相比,西药组和中药高剂量组能降低小鼠肺指数(P<0.05),其他组别能降低肺指数、升高胸腺指数和脾脏指数,但差异无统计学意义(P>0.05);解表清里方高、中剂量组能减轻小鼠肺部病变程度,西药组、解表清里方高、中剂量组能降低小鼠肺组织中M、NS2病毒基因复制水平(P<0.01或P<0.05);西药组和解表清里方高剂量组能降低小鼠肺组织中mTOR表达水平;西药组、解表清里方高剂量和中剂量组均能显著下调PI3K、AKT和GSK-3β蛋白和mRNA的表达水平(P<0.01或P<0.05)解表清里方低剂量组在各个方面与模型组相差不显著。结论:解表清里方甲型H1N1流感小鼠有抗病毒作用,其作用机制可能与抑制PI3K/AKT/GSK-3β信号通路中关键蛋白PI3K、AKT、GSK-3β、mTOR表达有关。

    Abstract:

    To investigate the mechanism of the antiviral action of Jiebiao Qingli Fang in mice with influenza A(H1N1).Methods:Thirty-six 7-week-old female BalB/c mice were randomly divided into the blank group,the model group,the western medicine group,and the high-dose,medium-dose,and low-dose groups of Jiebiao Qingli Fang by the random number method,with six mice in each group.The blank group was given an equal amount of saline nasal drops,and the rest of the mice were given influenza A virus solution in the left nostril at 50 μL.After 2 h of modeling,0.037 5 g/(kg·d) of oseltamivir phosphate was administered by gavage in the western medicine group,and 6.05 g/(kg·d),3.02 g/(kg·d),and 1.51 g/(kg·d) of Jiebiao Qingli Fang were administered to the high-dose group,the medium-dose group,and the low-dose group by gavage,respectively.The blank group and the model group were daily given saline 0.2 mL by gavage at the same time for five consecutive days.Lung index,thymus index,spleen index,pathological changes of lung tissue,expression of mammalian target of rapamycin(mTOR) in lung tissue,mRNA expression of the viral genes and phosphatidylinositol 3-kinase(PI3K),protein kinase B(AKT),and glycogen synthase kinase 3 beta(GSK-3β) in lung suspension,and protein expression of PI3K,AKT,and GSK-3β in lung tissue were compared between the two groups.Results:The results of animal experiments showed that compared with the model group,the western medicine group and the high-dose group of Jiebiao Qingli Fang were able to reduce the lung index of mice(P<0.05),and the other groups were able to reduce the lung index and increase the thymus index and spleen index,but the differences were not statistically significant(P>0.05).The high-dose and medium-dose groups of Jiebiao Qingli Fang were able to reduce the degree of lung lesions in mice,while the western medicine group and the high-dose and medium-dose groups of Jiebiao Qingli Fang were able to reduce the M and NS2 viral gene replication levels in lung tissue of mice(P<0.01 or P<0.05).The western medicine group and the high-dose group of Jiebiao Qingli Fang could reduce the expression level of mTOR in the lung tissue of mice.The western medicine group and the high-dose and medium-dose groups of Jiebiao Qingli Fang could significantly down-regulate the protein and mRNA expression levels of PI3K,AKT,and GSK-3β(P<0.01 or P<0.05).The difference between the low-dose group of Jiebiao Qingli Fang and the model group was not significant in all aspects.Conclusion:Jiebiao Qingli Fang has antiviral effects on mice with influenza A(H1N1),and its mechanism of action may be related to the inhibition of the expression of the key proteins PI3K,AKT,GSK-3β,and mTOR in the PI3K/AKT/GSK-3β signaling pathway.

    参考文献
    相似文献
    引证文献
引用本文

马一川,姚睿祺,明雨,晁燕,张洪春.解表清里方干预甲型H1N1流行性感冒小鼠的抗病毒作用机制[J].世界中医药,2024,(14).

复制
相关视频

分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2023-12-18
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2024-08-06
  • 出版日期:
文章二维码