Activation of PPARα by Wy-14643 ameliorates systemic lipopolysaccharide-induced acute lung injury

被引:24
作者
Yoo, Seong Ho [1 ,2 ]
Abdelmegeed, Mohamed A. [3 ]
Song, Byoung-Joon [3 ]
机构
[1] Seoul Natl Univ, Coll Med, Seoul Natl Univ Hosp, Biomed Res Inst, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Inst Forens Med, Seoul 110744, South Korea
[3] NIAAA, Lab Membrane Biochem & Biophys, Bethesda, MD USA
基金
新加坡国家研究基金会;
关键词
Peroxisome proliferator-activated receptor-alpha; Lipopolysaccharide; Acute lung injury; Cytokines; Nitroxidative stress; INFLAMMATION; EXPRESSION; AGONIST;
D O I
10.1016/j.bbrc.2013.05.073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Acute lung injury (ALI) is a major cause of mortality and morbidity worldwide. The activation of peroxisome proliferator-activated receptor-alpha (PPAR alpha) 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 PPAR alpha 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 PPAR alpha 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 PPAR alpha might have a therapeutic effect on LPS-induced ALI. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:366 / 371
页数:6
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