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纸质出版日期:2013
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王成阳, 李泽庚, 刘向国, 等. 六味补气胶囊对COPD肺气虚证模型STAT4,STAT6蛋白表达影响[J]. 中国实验方剂学杂志, 2013,19(21):194-198.
WANG Cheng-yang, LI Ze-geng, LIU Xiang-guo, et al. Effect of Liuwei Buqi Capsule on Expression of STAT4, STAT6 Protein in Rats Model with FQDS of COPD[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(21): 194-198.
王成阳, 李泽庚, 刘向国, 等. 六味补气胶囊对COPD肺气虚证模型STAT4,STAT6蛋白表达影响[J]. 中国实验方剂学杂志, 2013,19(21):194-198. DOI: 10.11653/syfj2013210194.
WANG Cheng-yang, LI Ze-geng, LIU Xiang-guo, et al. Effect of Liuwei Buqi Capsule on Expression of STAT4, STAT6 Protein in Rats Model with FQDS of COPD[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(21): 194-198. DOI: 10.11653/syfj2013210194.
目的: 观察六味补气胶囊对慢性阻塞性肺疾病(COPD)肺气虚证模型大鼠细胞信号转导转录因子(STAT)4
STAT6蛋白表达影响及机制。 方法: 将大鼠随机分为正常组、模型组、六味补气胶囊高剂量组(六高组)、六味补气胶囊低剂量组(六低组)、金水宝胶囊组(中药对照)、脾氨肽组(西药对照)
每组12只。除正常组外
其余大鼠采用烟熏加脂多糖(LPS)气管滴入方法建立COPD肺气虚证大鼠模型
模型复制成功第28天给药
各组给药剂量为:正常组、模型组:生理盐水0.09 g·kg-1;六高组:六味补气胶囊0.16 g·kg-1;六低组:六味补气胶囊0.04 g·kg-1;金水宝组:金水宝49.5 mg·kg-1
脾氨肽组:灌服脾氨肽0.033 mg·kg-1
1次/d
连续给药14 d。观察各组大鼠肺组织STAT4
STAT6蛋白表达变化。 结果: 与正常组比较
STAT4蛋白在COPD肺气虚证大鼠肺组织中表达的阳性面积增加、平均光密度增强 (P<0.01)
而STAT6蛋白表达的阳性面积减小、平均光密度降低(P<0.01);经六味补气胶囊等药治疗后
较之模型组
各治疗组STAT4的表达面积减小、强度减弱
STAT6的表达面积扩大(P<0.05)
各治疗组之间无明显差异。 结论: 六味补气胶囊可抑制COPD肺气虚证大鼠肺组织中STAT4蛋白表达
促进STAT6蛋白的表达。
Objective: To observe the influence of Liuwei Buqi capsule(LBC) on the expression of STAT4 and STAT6 protein and to study the therapeutic effects and possible mechanism in rat model with Fei-qi deficiency syndrome(FQDS) of chronic obstructive pulmonary disease(COPD). Method: The rats were randomly divided into normal group
model group
high dose of Liuwei Buqi group (0.16 g·kg-1)
low dose of Liuwei Buqi capsule group (0.04 g·kg-1)
Jinshuibao capsule group(49.5 mg·kg-1)
spleen aminopeptidase group(0.033 mg·kg-1)
(n=12). The rat model of lung deficiency of COPD was established by smoking rats and dripping the LPS into the trachea. At twenty-eight days after the modeling. corresponding drugs were given.The expression of STAT4 and STAT6 protein of lung tissue was observed. Result: Compared with the normal control group
the average optical density of STAT4 protein in lung tissue and the positive area in model group increased markedly
STAT6 protein decreased (P<0.01).Compared with the model group
the positive area of STAT4 became smaller and the average optical density became weaker
the positive area of STAT6 increased;meanwhile
no statistical significance was found among the treatment groups. Conclusion: The LBC can inhibit the expression of STAT4 protein
and promote the expression of STAT6 protein.
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