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PPARγas a Potential Target to Treat Airway Mucus Hypersecretion in Chronic Airway Inflammatory Diseases
Author(s) -
Yongchun Shen,
Lei Chen,
Tao Wang,
Fuqiang Wen
Publication year - 2012
Publication title -
ppar research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 49
eISSN - 1687-4765
pISSN - 1687-4757
DOI - 10.1155/2012/256874
Subject(s) - medicine , immunology , mucin , mucus , airway , inflammation , cystic fibrosis , transcription factor , peroxisome proliferator activated receptor , lung , asthma , receptor , pathology , biology , ecology , biochemistry , surgery , gene
Airway mucus hypersecretion (AMH) is a key pathophysiological feature of chronic airway inflammatory diseases such as bronchial asthma, cystic fibrosis, and chronic obstructive pulmonary disease. AMH contributes to the pathogenesis of chronic airway inflammatory diseases, and it is associated with reduced lung function and high rates of hospitalization and mortality. It has been suggested that AMH should be a target in the treatment of chronic airway inflammatory diseases. Recent evidence suggests that a key regulator of airway inflammation, hyperresponsiveness, and remodeling is peroxisome proliferator-activated receptor gamma (PPAR γ ), a ligand-activated transcription factor that regulates adipocyte differentiation and lipid metabolism. PPAR γ is expressed in structural, immune, and inflammatory cells in the lung. PPAR γ is involved in mucin production, and PPAR γ agonists can inhibit mucin synthesis both in vitro and in vivo . These findings suggest that PPAR γ is a novel target in the treatment of AMH and that further work on this transcription factor may lead to new therapies for chronic airway inflammatory diseases.

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