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黄芩苷对FM1肺炎小鼠肺损伤的作用机制研究

万巧凤 顾立刚 殷胜骏 吴珺 邱泽计

中国药理学通报2012,Vol.28Issue(2):208-212,5.
中国药理学通报2012,Vol.28Issue(2):208-212,5.DOI:10.3969/j.issn.1001-1978.2012.02.014

黄芩苷对FM1肺炎小鼠肺损伤的作用机制研究

Mechanism of Baicalin on lung tissue injuryof mice with FM1 induced pneumonia

万巧凤 1顾立刚 2殷胜骏 1吴珺 1邱泽计1

作者信息

  • 1. 北京中医药大学中医药抗病毒教育部重点实验室,北京,100029
  • 2. 宁夏医科大学,宁夏,银川,750004
  • 折叠

摘要

Abstract

Aim To explore mechanism of BAI on lung tissue injury of mice with FM1 induced pneumonia. Methods 96 ICR mice were randomly divided into normal group, model group, RBVgroup (100 mg · kg-1 · d-1 ), BAI groups ( 1500,750,375 mg · kg-1 · d-1 ),with 16 mice in each group. The model of mouse influenza virus pneumonia was prepared by infection of influenza virus strain A/FM/l/47( H1N1 ). Model mice were treated with different doses of BAI by intragastric administration. The pathological change of lung injury was observed; RT-PCR was adopted to determine the mRNA expressions of c-jun and c-fos; Western blot was used to determine the protein expressions of c-jun and p-c-jun; ELISA was applied to test the inflammatory cytokines in lung tissue homogenate.Results Compared with the model, BAI, at doses 750 mg ·kg-1 and 375 mg·kg-1, obviously alleviated the pathological change of lung injury, significantly down-regulated mRNA expressions of c-jun and c-fos ( P < 0. 05 , P < 0. 01 ), significantly downregulated protein expressions of c-jun and p-c-jun( P < 0. 01 )and also inhibited secretions of TNF-α and IL-1 β( P < 0. 01 ). Conclusions BAI can alleviate inflammatory pathological injury induced by FM1. It may inhibit the high expression of transcription factor AP-1 induced by influenza virus infection to decrease the secretion of inflammatory cytokines, and plays the function of anti-influenza virus infection.

关键词

黄芩苷/甲型流感病毒FM1/肺炎/c-jun/c-fos/RT-PCR/Western/blot

Key words

Baicalin/ influenza virus FM1/ pneumonia/c-jun/ c-fos/ RT-PCR/ Western blot

分类

医药卫生

引用本文复制引用

万巧凤,顾立刚,殷胜骏,吴珺 ,邱泽计..黄芩苷对FM1肺炎小鼠肺损伤的作用机制研究[J].中国药理学通报,2012,28(2):208-212,5.

基金项目

国家自然科学基金资助项目(No 30772872) (No 30772872)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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