| Literature DB >> 23727576 |
Seong Ho Yoo1, Mohamed A Abdelmegeed, Byoung-Joon Song.
Abstract
Acute lung injury (ALI) is a major cause of mortality and morbidity worldwide. The activation of peroxisome proliferator-activated receptor-α (PPARα) by its ligands, which include Wy-14643, has been implicated as a potential anti-inflammatory therapy. To address the beneficial efficacy of Wy-14643 for ALI along with systemic inflammation, the in vivo role of PPARα activation was investigated in a mouse model of lipopolysaccharide (LPS)-induced ALI. Using age-matched Ppara-null and wild-type mice, we demonstrate that the activation of PPARα by Wy-14643 attenuated LPS-mediated ALI. This was evidenced histologically by the significant alleviation of inflammatory manifestations and apoptosis observed in the lung tissues of wild-type mice, but not in the corresponding Ppara-null mice. This protective effect probably resulted from the inhibition of LPS-induced increases in pro-inflammatory cytokines and nitroxidative stress levels. These results suggest that the pharmacological activation of PPARα might have a therapeutic effect on LPS-induced ALI.Entities:
Keywords: ALI; Acute lung injury; Cytokines; LPS; Lipopolysaccharide; MDA; Nitroxidative stress; PPARα; Peroxisome proliferator-activated receptor-α; STAT1; acute lung injury; lipopolysaccharide; malondialdehyde; peroxisome proliferator-activated receptor-α; signal transducer and activator of transcription 1
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Year: 2013 PMID: 23727576 PMCID: PMC3869643 DOI: 10.1016/j.bbrc.2013.05.073
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575