肺痹汤2号对二氧化硫染毒小鼠肺氧化损伤的干预研究
Study on the impact of Feibitang-2 on SO2 induced oxidative stress mice
目的:观察肺痹汤2号对于二氧化硫染毒小鼠肺损伤的影响。方法:本实验建立了SO2(28±2mg/m3)吸入染毒的小鼠模型,并分别对中药治疗组与中药预防组进行了14天和28天的中药干预后,对小鼠肺组织丙二醇(MDA)、谷胱甘肽(GSH)含量和谷胱甘肽过氧化物酶(GSH-Px)、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)的活性影响进行检测,并对肺组织进行病理切片观察。结果:与空白组小鼠相比,模型组小鼠肺组织的MDA含量极显著升高(P<0.001),GSH含量与CAT的活性极显著降低(P<0.001),GSH-Px、SOD的活性显著降低(P<0.05)。中药治疗组、中药预防组小鼠与模型组小鼠相比,MDA含量减少,GSH含量提高,GSH-Px、SOD、CAT的活性有所恢复,但均不具有统计学差异。结论:肺痹汤2号可以促进SO2染毒小鼠肺组织炎性渗出的吸收,对SO2染毒小鼠肺组织的氧化损伤有一定的保护作用。
Mice were exposed to SO2 (28±2mg/m3) to induce oxidative stress; Traditional Chinese medicine (TCM) treatment group received intragastric administration of Feibitang-2 for 14 days and TCM prevention group received intragastric administration of Feibitang-2 for 28 days. Thereafter the mice were tested of the amount of content of propylene glycol (MDA) and glutathione (GSH) in lung tissues, and the impact on activity of glutathione peroxidase (GSH Px), superoxide dismutase (SOD) and catalase (CAT); pathological biopsy of lung tissues of the mice was observed. Results Comparing with control group, the amount of content of MDA in lung tissues of model group increased very significantly (P<0.001), GSH content and CAT activity decreased very significantly (P<0.001), the activity of GSH-Px, SOD decreased significantly (P<0.05). Comparing with model group, the amount of content of MDA of TCM treatment group and TCM prevention group decreased, GSH content increased, the activity of GSH-Px, SOD, and CAT recovered to some extent, though not statistically significant. Conclusions Feibitang-2 can improve the absorption of inflammatory exudation in lung tissues caused by SO2 exposure on mice; it also has a certain protective effect on oxidative stress of lung tissues caused by SO2 exposure.
曹芳、王玮、吴志松、马瑞鸿、焦扬
医药卫生理论中医学基础医学
二氧化硫肺痹汤2号抗氧化损伤实验研究
Sulfur dioxide Feibitang-2 Anti oxidative stress Experimental study
曹芳,王玮,吴志松,马瑞鸿,焦扬.肺痹汤2号对二氧化硫染毒小鼠肺氧化损伤的干预研究[EB/OL].(2016-08-10)[2025-08-04].http://www.paper.edu.cn/releasepaper/content/201608-71.点此复制
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