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首页|期刊导航|中国药理学通报|牡荆素减轻小鼠溃疡性结肠炎的药效作用及机制研究

牡荆素减轻小鼠溃疡性结肠炎的药效作用及机制研究

孙阿宁 任改艳 邓超 张晶晶 王峥涛 窦薇

中国药理学通报Issue(12):1677-1680,1681,5.
中国药理学通报Issue(12):1677-1680,1681,5.DOI:10.3969/j.issn.1001-1978.2014.12.012

牡荆素减轻小鼠溃疡性结肠炎的药效作用及机制研究

Effects and mechanisms of vitexin against ulcerative colitis in mice

孙阿宁 1任改艳 2邓超 3张晶晶 3王峥涛 3窦薇1

作者信息

  • 1. 中国药科大学生药学研究室,江苏 南京 210038
  • 2. 上海中医药大学中药研究所中药标准化教育部重点实验室暨上海市复方中药重点实验室,上海 201203
  • 3. 上海中医药大学中药研究所中药标准化教育部重点实验室暨上海市复方中药重点实验室,上海 201203
  • 折叠

摘要

Abstract

Aim To evaluate the effect and mecha-nism of vitexin in a mouse model of DSS-induced ulcer-ative colitis (UC).Methods C57BL/6 mice were randomly placed into three groups: normal control group,DSS group and DSS +Vitexin group.Mice coli-tis was induced by adding 4% dextran sulphate sodium (DSS)into the drinking water for seven days.Vitexin was administered once a day along with DSS treatment. Mice were monitored daily with body weight change and diarrhea symptoms.After sacrifice,colon was re-moved and fixed in 1 0% (W/V)buffered formalin for hematoxylin-eosin (H&E)staining.Histological dam-age was assessed as a combined score of inflammatory cell infiltration and mucosal damage.The remaining colon pieces were collected to measure the activity of myeloperoxidase (MPO)by ELISA method and to de-termine the mRNA expression of TNF-α,IL-6 and COX-2.Results None of the mice receiving vehicle alone exhibited body weight loss and mucosal disrup-tion at any point during the study.Vitexin treatment significantly ameliorated DSS-induced body weight loss and histological score.The activity of MPO and the mRNA expression of TNF-α,IL-6 and COX-2 were markedly inhibited by vitexin treatment.Conclusion Vitexin ameliorates DSS-induced colitis through sup-pressing leukocyte infiltration and pro-inflammatory mediators production.

关键词

牡荆素/溃疡性结肠炎/葡聚糖硫酸钠/MPO/TNF-α/IL-6/COX-2

Key words

vitexin/ulcerative colitis/dextran sul-phate sodium/MPO/TNF-α/IL-6/COX-2

分类

医药卫生

引用本文复制引用

孙阿宁,任改艳,邓超,张晶晶,王峥涛,窦薇..牡荆素减轻小鼠溃疡性结肠炎的药效作用及机制研究[J].中国药理学通报,2014,(12):1677-1680,1681,5.

基金项目

国家自然科学基金资助项目(No 81273572);上海市教委科研创新项目(No 13YZ043);上海市自然科学基金资助项目 ()

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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