Inhalation of glycopyrronium inhibits cigarette smoke-induced acute lung inflammation in a murine model of COPD

被引:31
|
作者
Shen, Liang-liang [1 ,2 ]
Liu, Ya-nan [1 ,2 ]
Shen, Hui-juan [2 ]
Wen, Chong
Jia, Yong-liang [2 ]
Dong, Xin-wei [2 ]
Jin, Fang
Chen, Xiao-ping [3 ,4 ]
Sun, Yun [1 ]
Xie, Qiang-min [2 ,5 ]
机构
[1] Yangzhou Univ, Coll Med, Yangzhou City 225001, Jiangsu, Peoples R China
[2] Zhejiang Univ, Sch Med, State Food & Drug Adm China, Zhejiang Resp Drugs Res Lab, Hangzhou 310058, Zhejiang, Peoples R China
[3] Shanghai Inst Pharmaceut Ind, Shanghai 200040, Peoples R China
[4] Jiashilianbo Med Sci & Tech Co, Beijing 100080, Peoples R China
[5] Zhejiang Univ, Lab Anim Ctr, Hangzhou 310058, Zhejiang, Peoples R China
关键词
Glycopyrronium bromide; Drug delivery; Muscarinic receptor antagonist; Cigarette smoke; Airway inflammation; COPD; OBSTRUCTIVE PULMONARY-DISEASE; NONNEURONAL CHOLINERGIC SYSTEM; ONCE-DAILY NVA237; OXIDATIVE STRESS; MATRIX METALLOPROTEINASES; ACETYLCHOLINE; TIOTROPIUM; AIRWAYS; PHARMACOKINETICS; PATHOGENESIS;
D O I
10.1016/j.intimp.2013.12.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Glycopyrronium bromide (GB) is a muscarinic receptor antagonist that has been used as a long-acting bronchodilator in chronic obstructive pulmonary disease (COPD) patients. The aim of this study was to investigate the anti-inflammatory activity of inhaled GB in a cigarette smoke-induced acute lung inflammation mouse model. We found that aerosol pre-treatment with GB suppresses the accumulation of neutrophils and macrophages in the bronchoalveolar lavage fluid (BALF) in cigarette smoke (CS)-exposed mice. GB at doses of 300 and 600 mu g/ml significantly inhibited the CS-induced increases in the mRNA and protein expression levels of interleukin (IL)-1 beta tumor necrosis factor (TNF)-alpha, monocyte chemotactic protein (MCP)-1 and transforming growth factor (TGF)-beta 1 in lung tissues and the BALF. Moreover, GB at a dose of 600 mu g/ml significantly inhibited the CS-induced changes in glutathione (GSH) and myeloperoxidase (MPO) activities in the BALF, decreased the CS-induced expression of matrix metalloproteinases (MMP)-9, and increased the CS-induced expression of tissue inhibitor of metalloproteinases (TIMP)-1, as determined through the immunohistochemical staining of lung tissue. Our results demonstrate the beneficial effects of inhaled GB on the inflammatory reaction in COPD. (C) 2013 Published by Elsevier B.V.
引用
收藏
页码:358 / 364
页数:7
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