首页|复方佛耳草合剂对慢性阻塞性肺疾病大鼠TLR4/MyD88/NF-κB信号通路的影响

复方佛耳草合剂对慢性阻塞性肺疾病大鼠TLR4/MyD88/NF-κB信号通路的影响

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目的 探讨复方佛耳草合剂对慢性阻塞性肺疾病(COPD)大鼠TLR4/MyD88/NF-κB信号通路的影响.方法 大鼠随机分为空白组(10 只)和造模组(50 只),造模组连续 12 周采用香烟烟雾联合气管注射LPS建立COPD大鼠模型.将造模成功的大鼠随机分为模型组、地塞米松组(0.5 mg/kg)和复方佛耳草合剂低、中、高剂量组(6.8、13.6、27.2 g/kg),每组 10 只.给药干预24 周后,采用动物肺功能仪检测大鼠肺功能,HE染色法观察肺组织病理变化,ELISA法检测血清TNF-α、IL-1β、IL-6、MDA水平及SOD活性,RT-qPCR法检测肺组织TLR4、MyD88、NF-κB及caspase-3 mRNA表达,Western blot法检测肺组织TLR4、MyD88、NF-κB及TNF-α蛋白表达.结果 与空白组比较,模型组大鼠存在肺通气功能障碍,肺组织和支气管受损明显,SOD活性降低(P<0.01),血清TNF-α、IL-1β、IL-6 及MDA水平升高(P<0.01),肺组织TLR4、MyD88、NF-κB、caspase-3 mRNA表达和TLR4、MyD88、NF-κB、TNF-α蛋白表达均升高(P<0.01);与模型组比较,复方佛耳草合剂各剂量组均能够改善肺功能指标,修复受损肺组织,降低血清TNF-α、IL-1β、IL-6及MDA水平(P<0.05,P<0.01),降低肺组织TLR4、MyD88、NF-κB、caspase-3 mRNA表达和 TLR4、MyD88、NF-κB、TNF-α 蛋白表达(P<0.05,P<0.01),且复方佛耳草合剂的作用呈剂量依赖性.结论 复方佛耳草合剂可改善慢性阻塞性肺疾病大鼠的肺功能障碍与病理损伤,其机制可能与调控TLR4/MyD88/NF-κB信号通路相关.
Effects of Compound Fo'ercao Mixture on TLR4/MyD88/NF-κB signaling pathway in a rat model of chronic obstructive pulmonary disease
AIM To explore the effect of Compound Fo'ercao Mixture on TLR4/MyD88/NF-κB signaling pathway in a rat model of chronic obstructive pulmonary disease(COPD).METHODS Rats were randomly divided into the blank group(n=10),and the model group(n=50)for the establishment of a rat model of COPD by 12-week cigarette smoke exposure combined with intratracheal injection of LPS.The successful rat models were randomly divided into the model group,the dexamethasone group(0.5 mg/kg)and the low,medium and high dose Compound Fo'ercao Mixture groups(6.8,13.6 and 27.2 g/kg),with 10 rats in each group.After 24 weeks of drug intervention,the rats had their lung function detected by animal lung function meter;their pathological changes of lung tissue observed by HE staining;their serum TNF-α,IL-1β,IL-6,and MDA levels and SOD activity detected by ELISA;their pulmonary mRNA expressions of TLR4,MyD88,NF-κB and caspase-3 detected by RT-qPCR;and their pulmonary protein expressions of TLR4,MyD88,NF-κB and TNF-α detected by Western blot.RESULTS Compared with the blank group,the model group displayed obviously pulmonary ventilation dysfunction,damaged lung tissue and bronchus,decreased SOD activity(P<0.01);increased serum TNF-α,IL-1β,IL-6 and MDA levels(P<0.01);and increased pulmonary expressions of TLR4,MyD88,NF-κB and caspase-3 mRNA and TLR4,MyD88,NF-κB and TNF-α proteins(P<0.01).Compared with the model group,all Compound Fo'ercao Mixture groups shared improvement in lung function indices levels and lung tissue damage;decrease in the levels of serum TNF-α,IL-1β,IL-6 and MDA(P<0.05,P<0.01);and decrease in the pulmonary expressions of TLR4,MyD88,NF-κB and caspase-3 mRNA and TLR4,MyD88,NF-κB and TNF-α protein(P<0.05,P<0.01)in a dose-dependent manner.CONCLUSION Compound Fo'ercao Mixture can improve the lung dysfunction and pathological injury in a rat model of COPD,and its mechanism may be associated with the regulated TLR4/MyD88/NF-κB signaling pathway.

Compound Fo'ercao Mixturechronic obstructive pulmonary diseaseoxidative stressinflammatory factorTLR4/MyD88/NF-κB signaling pathway

廖健杉、折哲、李凤森、石克华

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上海中医药大学附属市中医医院,上海 200071

上海中医药大学附属第七人民医院,上海 200137

新疆维吾尔自治区中医医院,新疆 乌鲁木齐 830000

复方佛耳草合剂 慢性阻塞性肺疾病 氧化应激 炎症因子 TLR4/MyD88/NF-κB信号通路

国家中医药局专项

JDZX2015231

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(3)
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