Azithromycin inhibits nontypeable Haemophilus influenzae-induced MUC5AC expression and secretion via inhibition of activator protein-1 in human airway epithelial cells

被引:30
作者
Araki, Nobuko [1 ]
Yanagihara, Katsunori [1 ,2 ]
Morinaga, Yoshitomo [1 ,2 ]
Yamada, Koichi [1 ,2 ]
Nakamura, Shigeki [2 ]
Yamada, Yasuaki [1 ]
Kohno, Shigeru [2 ,3 ]
Kamihira, Shimeru [1 ]
机构
[1] Nagasaki Univ, Dept Lab Med, Grad Sch Biomed Sci, Nagasaki 8528102, Japan
[2] Nagasaki Univ, Dept Internal Med 2, Grad Sch Biomed Sci, Nagasaki 8528102, Japan
[3] Nagasaki Univ, Global COE Program, Nagasaki 8528102, Japan
关键词
Mucus; Mucin; Chronic obstructive pulmonary disease; Immunomodulatory effect; Macrolides; NF-KAPPA-B; CYSTIC-FIBROSIS; MUCIN TRANSCRIPTION; NCI-H292; CELLS; CLARITHROMYCIN; ERYTHROMYCIN; RESPONSES; DISEASE; TRIAL;
D O I
10.1016/j.ejphar.2010.06.056
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nontypeable Haemophilus influenzae (NTHi) is one of the most common pathogens in chronic airway infections and exacerbation. The hallmark of chronic respiratory diseases, including cystic fibrosis, diffuse panbronchiolitis and chronic obstructive pulmonary disease, is mucin overproduction. Prolonged macrolide antibiotic therapy at low doses is known to improve clinical outcome in patients with chronic respiratory diseases via anti-inflammatory effects. In this study, we investigated the effects of macrolide therapy on NTHi-induction of the MUC5AC mucin in human airway epithelial cells. A 15-membered macrolide, azithromycin, but not a 14-membered macrolide, clarithromycin, inhibited NTHi-induction of MUC5AC at both the mRNA and protein levels through selective suppression of activation of the transcription factor activator protein-1. Our findings suggest that each macrolide affects MUC5AC production in different ways and that azithromycin is more suitable for the treatment of NTHi-induced respiratory infection. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:209 / 214
页数:6
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