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柴葛芩连汤对幼年小鼠肺炎模型治疗作用及其机制
引用本文:边红恩,陈团营.柴葛芩连汤对幼年小鼠肺炎模型治疗作用及其机制[J].中国实验方剂学杂志,2020,26(4):23-28.
作者姓名:边红恩  陈团营
作者单位:河南中医药大学 第二附属医院, 郑州 450000,河南中医药大学 第二附属医院, 郑州 450000
基金项目:河南省科技厅技术研究计划项目(142300410070)
摘    要:目的:观察柴葛芩连汤对肺炎幼年小鼠(幼鼠)模型的治疗作用,并探讨其相关的作用机制。方法:以金黄色葡萄球菌经幼鼠鼻孔缓慢滴入小鼠鼻腔内的方法复制肺炎模型,造模成功后将幼鼠随机分为模型组、克林霉素组、柴葛芩连汤高、低剂量组,并以假手术组作为阴性组。造模后当天开始给药,柴葛芩连汤高、低剂量200,100 mg·kg^-1,克林霉素120 mg·kg^-1。每天观察幼鼠状况,5 d后对每组幼鼠的肺脏进行菌落计数,采用酶联免疫吸附测定(ELISA)检测每组小鼠的肺脏灌洗液中白细胞介素(IL)-16,肿瘤坏死因子(TNF)-α的表达水平,采用实时荧光定量聚合酶链式反应(Real-time PCR)及蛋白免疫印迹法(Western blot)测量幼鼠肺中肿瘤坏死因子受体(TNFR)1,半胱氨酸的天冬氨酸蛋白水解酶(Caspase)-3,Caspase-7 mRNA及蛋白的表达,并观察肺脏的病理学改变。结果:与假手术组比较,造模幼鼠呼吸状态及活动状态较差,给药后均有不同程度改善,其中以柴葛芩连汤高剂量组存活率较高。与假手术组比较,模型组幼鼠肺内菌落计数均有所增加;与模型组比较,克林霉素组、柴葛芩连汤高剂量组肺内菌落计数改善较明显(P<0.05,P<0.01)。与假手术组比较,模型组IL-16,TNF-α的表达水平及肺中TNFR1,Caspase-3,Caspase-7 mRNA和蛋白的表达水平均显著升高(P<0.01),而与模型组比较,克林霉素组、柴葛芩连汤高、低剂量组IL-16,TNF-α的表达水平及肺中TNFR1,Caspase-3,Caspase-7 mRNA和蛋白的表达水平均明显下降(P<0.05,P<0.01),且肺脏病理学改变有所改善,克林霉素组、柴葛芩连汤高剂量组改善较明显。结论:柴葛芩连汤对金黄色葡萄球菌肺炎幼鼠模型具有一定的治疗作用,该作用可能与调控TNFR1,Caspase-3,Caspase-7通路,减少IL-16,TNF-α的分泌,增强对金黄色葡萄球菌的清除有关。

关 键 词:肺炎幼年小鼠模型  柴葛芩连汤  金黄色葡萄球菌  白细胞介素-16(IL-16)  肿瘤坏死因子受体1
收稿时间:2019/6/5 0:00:00

Therapeutic Effect and Mechanism of Chaige Qinlian Tang on Young Mouse MRSA Pneumonia Model
BIAN Hong-en and CHEN Tuan-ying.Therapeutic Effect and Mechanism of Chaige Qinlian Tang on Young Mouse MRSA Pneumonia Model[J].China Journal of Experimental Traditional Medical Formulae,2020,26(4):23-28.
Authors:BIAN Hong-en and CHEN Tuan-ying
Institution:Second Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450000, China and Second Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou 450000, China
Abstract:Objective:To explore the therapeutic effect and mechanism of Chaige Qinlian Tang on pneumonia in young mice.Method:The pneumonia model was duplicated by slowly dripping Staphylococcus aureus into the nasal cavity of mice.After successful modeling,the mice were randomly divided into model group,clindamycin group,and high and low-dose Chaige Qinlian Tang groups,with sham operation group as negative control group.The rats were given 200 mg·kg^-1 high-dose Chaige Qinlian Tang,100 mg·kg^-1 low-dose Chaige Qinlian Tang and 120 mg·kg^-1 clindamycin.The mice were observed every day.Colonies were counted in the lungs of each group five days later.The expression levels of interleukin(IL)-16,tumor necrosis factor(TNF)-αin lung lavage fluid of each group were determined by enzyme linked immunosorbent assay(ELISA).Real-time fluorescent quantitative polymerase chain reaction(Real-time PCR)and Western blot were used to measure the expression levels of IL-16,TNF-αin lung lavage fluid of each group.The expressions of tumor necrosis factor receptor(TNFR)1,Caspase-3 and Caspase-7 in lung and the pathological changes of lung were observed.Result:Compared with the sham operation group,the respiratory state and the activity state of the model mice were worse,and the survival rate was higher in the high-dose Chaige Qinlian Tang group.Compared with the sham operation group,the pulmonary colony counts in the model group and treatment groups were increased,compared with the model group,the lung colony counts in clindamycin group and high-dose Chaige Qinlian Tang group were improved significantly(P<0.05,P<0.01).Compared with the control group,the expression levels of IL-16,TNF-α,TNFR1,Caspase-3,Caspase-7 mRNA and protein in the lung of model group and treatment groups were significantly increased(P<0.01).Compared with model group,the expression levels of IL-16,TNF-αand TNFR1,Caspase-3,Caspase-7 in the lung of clindamycin group and high and low-dose Chaige Qinlian Tang groups were significantly increased(P<0.01).The expression levels of protein and mRNA were significantly decreased(P<0.05,P<0.01),and the pathological changes of lung were improved,especially in clindamycin group and high-dose Chaige Qinlian Tang group.Conclusion:Chaige Qinlian Tang has a certain therapeutic effect on Staphylococcus aureus pneumonia in young mice.This effect may be related to regulating TNFR1,Caspase-3 and Caspase-7 pathways,reducing the secretion of IL-16 and TNF-alpha,and enhancing the clearance of staphylococcus aureus.
Keywords:pneumonia young mice model  Chaige Qinlian Tang  staphylococcus aureus  interleukin-16(IL-16)  tumor necrosis factor receptor 1(TNFR1)
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