Liu Renping, Wang Peihong, Wu Caiqing, Chen Juan, Li Chengxin, Xie Yongtao, Wang Qi, Liu Jianming, He Huan, Zhu Jing
Medical Experiment Education Department, Medical College of Nanchang University, Nanchang, Jiangxi 330031, P.R. China.
Department of Pharmacology, Jiangxi Medical College, Shangrao, Jiangxi 334000, P.R. China.
Exp Ther Med. 2018 Apr;15(4):3385-3391. doi: 10.3892/etm.2018.5851. Epub 2018 Feb 8.
Willd (HDW) is a constituent of several Chinese medicines used clinically to treat inflammatory diseases, including airway inflammation. The aim of the present study was to investigate whether HDW serves a protective role in suppressing chronic airway inflammation and its underlying mechanisms. A mouse model of chronic smoking was induced via exposure to cigarette smoke (CS) for 30 days, increasing the exposure time for up to 5 min per day and the administration of lipopolysaccharide (LPS). Mice were gavaged with HDW (50 or 100 mg/kg body weight), dexamethasone (1 mg/kg body weight) or normal saline (NS, 0.9%) 1 h prior to CS challenge. Compared with CS and LPS (SL)-induced mice, the levels of interleukin (IL)-1β, tumor necrosis factor-α and transforming growth factor-β in bronchoalveolar lavage fluid from HDW+SL mice were significantly decreased and IL-10 was markedly reduced. Histological examination of the lung tissues revealed that HDW treatment alleviates airway inflammation. In addition, the administration of HDW to human bronchial epithelial BEAS-2B cells suppressed the activity of the nuclear factor (NF)-κB signaling pathway. The results of the present study demonstrate that HDW has a therapeutic effect in COPD and the underlying mechanism may be attributed to inhibition of the NF-κB pathway.
威灵仙(HDW)是几种临床上用于治疗炎症性疾病(包括气道炎症)的中药的成分。本研究的目的是探讨HDW在抑制慢性气道炎症中是否起保护作用及其潜在机制。通过每天暴露于香烟烟雾(CS)30天,每天增加暴露时间至5分钟并给予脂多糖(LPS),诱导慢性吸烟小鼠模型。在CS攻击前1小时,给小鼠灌胃HDW(50或100mg/kg体重)、地塞米松(1mg/kg体重)或生理盐水(NS,0.9%)。与CS和LPS(SL)诱导的小鼠相比,HDW+SL小鼠支气管肺泡灌洗液中白细胞介素(IL)-1β、肿瘤坏死因子-α和转化生长因子-β水平显著降低,IL-10明显升高。肺组织的组织学检查显示,HDW治疗减轻了气道炎症。此外,将HDW给予人支气管上皮BEAS-2B细胞可抑制核因子(NF)-κB信号通路的活性。本研究结果表明,HDW对慢性阻塞性肺疾病具有治疗作用,其潜在机制可能归因于对NF-κB通路的抑制。