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Azithromycin inhibits nontypeable Haemophilus influenzae-induced MUC5AC expression and secretion via inhibition of activator protein-1 in human airway epithelial cells
- Source :
- European journal of pharmacology. 644(1-3):209-214
- Publication Year :
- 2010
- Publisher :
- Elsevier BV, 2010.
-
Abstract
- 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.<br />European journal of pharmacology, 644(1-3), pp.209-214; 2010
- Subjects :
- Haemophilus Infections
Immunomodulatory effect
Biology
Azithromycin
Mucin 5AC
medicine.disease_cause
Cystic fibrosis
Haemophilus influenzae
Microbiology
Clarithromycin
Cell Line, Tumor
medicine
otorhinolaryngologic diseases
Humans
RNA, Messenger
Pharmacology
Chronic obstructive pulmonary disease
Respiratory disease
Respiratory infection
Epithelial Cells
medicine.disease
Anti-Bacterial Agents
Transcription Factor AP-1
Mucus
medicine.anatomical_structure
Immunology
Mucin
Macrolides
Diffuse panbronchiolitis
medicine.drug
Respiratory tract
Subjects
Details
- Language :
- English
- ISSN :
- 00142999
- Volume :
- 644
- Issue :
- 1-3
- Database :
- OpenAIRE
- Journal :
- European journal of pharmacology
- Accession number :
- edsair.doi.dedup.....57768db68b2e0f9b4c47a8ef61a32478