| Literature DB >> 26702150 |
Rui-Ming Liu1, Stephanie Eldridge2, Nobuo Watanabe3, Jessy Deshane2, Hui-Chien Kuo4, Chunsun Jiang2, Yong Wang2, Gang Liu2, Lisa Schwiebert5, Toshio Miyata3, Victor J Thannickal2.
Abstract
Asthma is one of the most common respiratory diseases. Although progress has been made in our understanding of airway pathology and many drugs are available to relieve asthma symptoms, there is no cure for chronic asthma. Plasminogen activator inhibitor 1 (PAI-1), a primary inhibitor of tissue-type and urokinase-type plasminogen activators, has pleiotropic functions besides suppression of fibrinolysis. In this study, we show that administration of TM5275, an orally effective small-molecule PAI-1 inhibitor, 25 days after ovalbumin (OVA) sensitization-challenge, significantly ameliorated airway hyperresponsiveness in an OVA-induced chronic asthma model. Furthermore, we show that TM5275 administration significantly attenuated OVA-induced infiltration of inflammatory cells (neutrophils, eosinophils, and monocytes), the increase in the levels of OVA-specific IgE and Th2 cytokines (IL-4 and IL-5), the production of mucin in the airways, and airway subepithelial fibrosis. Together, the results suggest that the PAI-1 inhibitor TM5275 may have therapeutic potential for asthma through suppressing eosinophilic allergic response and ameliorating airway remodeling.Entities:
Keywords: animal model; plasminogen activator inhibitor 1; plasminogen activator inhibitor 1 inhibitor
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Year: 2015 PMID: 26702150 PMCID: PMC4754904 DOI: 10.1152/ajplung.00217.2015
Source DB: PubMed Journal: Am J Physiol Lung Cell Mol Physiol ISSN: 1040-0605 Impact factor: 5.464