首页|苏黄止咳胶囊中白花前胡甲素对咳嗽变异性哮喘的改善作用

苏黄止咳胶囊中白花前胡甲素对咳嗽变异性哮喘的改善作用

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目的 探讨苏黄止咳胶囊中白花前胡甲素对咳嗽变异性哮喘(CVA)的影响.方法 将大鼠随机分为正常组、模型组、地塞米松组(0.5 mg/kg)、苏黄止咳胶囊组(7 g/kg)和白花前胡甲素低、中、高剂量组(15、30、60 mg/kg),采用腹腔注射致敏剂(1 mg/mL卵清蛋白和 10 mg/mL氢氧化铝)和雾化吸入 1%卵清蛋白的方法构建CVA大鼠模型,第 14 天起灌胃给予相应剂量药物,给药 14d后,HE、Masson和PAS染色观察肺组织病理变化,血细胞分析仪检测大鼠支气管肺泡灌洗液(BALF)中炎症细胞数,ELISA法检测BALF中IL-4、IL-5、IL-13、MUC5AC水平.采用脂多糖(LPS)诱导建立RAW264.7 细胞炎症模型,分别以 4、8、16 μmol/L白花前胡甲素和 0.25 mg/mL苏黄止咳胶囊处理,Griess法检测细胞中NO水平,荧光显微镜下观察细胞中ROS表达.RT-qPCR法检测肺组织和细胞中 IL-6、IL-1β、COX-2、iNOS、PPAR-γ mRNA 表达,Western blot 法检测肺组织和细胞中 p-P65、P65、p-IκBα、IκBα、NLRP3、caspase-1(p20)、IL-1β蛋白表达.结果 体内实验结果表明,白花前胡甲素能减少CVA大鼠咳嗽次数(P<0.01),延长咳嗽潜伏期(P<0.05,P<0.01),减少BALF中嗜酸性粒细胞和中性粒细胞数(P<0.05,P<0.01),降低BALF中IL-4、IL-5、IL-13、MUC5AC水平(P<0.01)和肺组织中IL-6、IL-1β、COX-2、iNOS mRNA表达(P<0.05,P<0.01),降低 P65、IκBα 蛋白磷酸化及 NLRP3、caspase-1(p20)、IL-1β 蛋白表达(P<0.05,P<0.01).体外实验结果表明,白花前胡甲素能抑制LPS诱导的RAW264.7 细胞中NO的释放,降低细胞中ROS水平(P<0.01);降低细胞中IL-1β、COX-2、iNOS mRNA表达(P<0.05,P<0.01),升高PPAR-γ mRNA表达(P<0.05),降低P65、IκBα蛋白磷酸化和NLRP3 蛋白表达(P<0.05,P<0.01).结论 白花前胡甲素可能是通过抑制NF-κB信号通路活化并降低NLRP3 炎症小体的表达,发挥抗炎和止咳作用,从而改善咳嗽变异性哮喘,是苏黄止咳胶囊的主要止咳功效成分之一.
Ameliorative effects of praeruptorin A from Suhuang antitussive capsules on cough variant asthma
AIM To explore the effects of praeruptorin A from Suhuang antitussive capsules on cough variant asthma(CVA).METHODS The rats were randomly divided into the normal group,the model group,the dexamethasone group(0.5 mg/kg),the Suhuang antitussive capsules group(7 g/kg)and the low,medium and high dose praeruptorin A groups(15,30 and 60 mg/kg).The rat model of CVA was established by intraperitoneal injection of sensitizer(1 mg/mL ovalbumin and 10 mg/mL aluminum hydroxide)and aerosol inhalation of 1%ovalbumin followed by the corresponding dosing of drugs by gavage initiated on the 14th day.Another 14 days later,the rats had their pathological pulmonary changes observed by HE,Masson and PAS stainings;their number of inflammatory cells in bronchoalveolar lavage fluid(BALF)detected by hematology analyzer;and their levels of IL-4,IL-5,IL-13 and MUC5AC in BALF detected by ELISA.The RAW264.7 cell inflammatory model induced by lipopolysaccharide(LPS)was treated with 4,8,16 μmol/L praeruptorin A or 0.25 mg/mL Suhuang antitussive capsules,respectively.And the cells had their NO level detected by Griess method,and their ROS expression observed using fluorescence microscopy.The detections of the pulmonary and cellular mRNA expressions of IL-6,IL-1β,COX-2,iNOS and PPAR-γ by RT-qPCR;and the protein expressions of p-P65,P65,p-IκBα,IκBα,NLRP3,caspase-1(p20)and IL-1β by Western blot were conducted in both the cells and the rats.RESULTS The in vivo result showed that praeruptorin A reduced the cough frequency(P<0.01);prolonged the cough latency(P<0.05,P<0.01);reduced the number of eosinophils and neutrophils in BALF(P<0.05,P<0.01);decreased the levels of IL-4,IL-5,IL-13 and MUC5AC in BALF and the pulmonary mRNA expressions of IL-6,IL-1β,COX-2 and iNOS(P<0.05,P<0.01);and decreased the phosphorylation of P65 and IκBα protein and NLRP3,caspase-1(p20)and IL-1β protein expressions(P<0.05,P<0.01)as well.The in vitro result showed that praeruptorin A inhibited the release of LPS-induced NO and reduce the ROS level(P<0.01);decreased the mRNA expressions of IL-1β,COX-2 and iNOS(P<0.05,P<0.01);increased PPAR-γ mRNA expression(P<0.05),and decreased the phosphorylation of P65 and IκBα protein and the expression of NLRP3 protein(P<0.05,P<0.01).CONCLUSION Praeruptorin A,one of the main antitussive components of Suhuang antitussive capsules,may improve CVA because of its anti-inflammatory and antitussive role by inhibiting the activation of NF-κB signaling pathway and reducing the expression of NLRP3 inflammatory corpuscles.

praeruptorin ASuhuang antitussive capsulescough variant asthma(CVA)NF-κBNLRP3inflammation

赵子瑶、江宏、欧永玉、陈孝源、吴楠、白子玉、张之昊、谭宁华

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中国药科大学中药学院,江苏 南京 211198

扬子江药业集团北京海燕药业有限公司,北京 102206

白花前胡甲素 苏黄止咳胶囊 咳嗽变异性哮喘(CVA) NF-κB NLRP3 炎症

国家自然科学基金项目

32070356

2024

中成药
国家食品药品监督管理局,信息中心中成药信息站,上海中药行业协会

中成药

CSTPCD北大核心
影响因子:1.217
ISSN:1001-1528
年,卷(期):2024.46(9)
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