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Respir Res ; 23(1): 128, 2022 May 20.
Article in English | MEDLINE | ID: mdl-35596212

ABSTRACT

BACKGROUND: Pulmonary fibrosis is a progressive and usually lethal pulmonary disease. Despite considerable research efforts, no effective therapeutic strategy for pulmonary fibrosis has been developed. NecroX-5 has been reported to possess anti-inflammatory, anti-oxidative and anti-tumor activities. In the present study, we aimed to determine whether NecroX-5 exhibits antifibrotic property in bleomycin (BLM)-induced pulmonary fibrosis. RESULTS: We found that pre-treatment with NecroX-5 alleviated inflammatory response, reduced oxidative stress, inhibited epithelial-mesenchymal transition (EMT), and ameliorated pulmonary fibrosis in vivo and in vitro. Our data further indicated that NecroX-5 substantially reduced activation of NLRP3 inflammasome and TGF-ß1/Smad2/3 signaling in vivo and in vitro. Additionally, NLRP3 overexpression significantly reversed the protective effects of NecroX-5 in lung epithelial cells exposed to BLM. CONCLUSIONS: Overall, our results demonstrate the potent antifibrotic properties of NecroX-5 and its therapeutic potential for pulmonary fibrosis.


Subject(s)
Epithelial-Mesenchymal Transition , Heterocyclic Compounds, 4 or More Rings , NLR Family, Pyrin Domain-Containing 3 Protein , Pulmonary Fibrosis , Sulfones , Animals , Bleomycin , Epithelial-Mesenchymal Transition/drug effects , Heterocyclic Compounds, 4 or More Rings/pharmacology , Mice , NLR Family, Pyrin Domain-Containing 3 Protein/metabolism , Pulmonary Fibrosis/chemically induced , Pulmonary Fibrosis/drug therapy , Pulmonary Fibrosis/pathology , Sulfones/pharmacology , Transforming Growth Factor beta1/metabolism
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