In vivo evidence of free radical generation in the mouse lung after exposure to Pseudomonas aeruginosa bacterium: An ESR spin-trapping investigation

被引:6
作者
Sato, Keizo [2 ]
Corbett, Jean [1 ]
Mason, Ronald P. [1 ]
Kadiiska, Maria B. [1 ]
机构
[1] NIEHS, Lab Toxicol & Pharmacol, NIH, Res Triangle Pk, NC 27709 USA
[2] Kyushu Univ Hlth & Welf, Sch Pharmaceut Sci, Dept Biochem 1, Nobeoka, Japan
基金
美国国家卫生研究院;
关键词
free radicals; mice; Pseudomonas aeruginosa pneumonia; NADPH-oxidase; xanthine-oxidase; XANTHINE-OXIDASE; LIPID-PEROXIDATION; GENE-EXPRESSION; NADPH OXIDASE; HOST-DEFENSE; NITRIC-OXIDE; INJURY; DESFERRIOXAMINE; RESONANCE; CELLS;
D O I
10.3109/10715762.2012.667089
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
In the Pseudomonas aeruginosa-induced rodent pneumonia model, it is thought that free radicals are significantly associated with the disease pathogenesis. However, until now there has been no direct evidence of free radical generation in vivo. Here we used electron spin resonance (ESR) and in vivo spin trapping with alpha-(4-pyridyl-1-oxide)-N-tert-butylnitrone to investigate free radical production in a murine model. We detected and identified generation of lipid-derived free radicals in vivo (a(N) = 14.86 +/- 0.03 G and a(H)beta = 2.48 +/- 0.09 G). To further investigate the mechanism of lipid radical production, we used modulating agents and knockout mice. We found that with GdCl3 (phagocytic toxicant), NADPH-oxidase knockout mice (Nox2(-/-)), allopurinol (xanthine-oxidase inhibitor) and Desferal (metal chelator), generation of lipid radicals was decreased; histopathological and biological markers of acute lung injury were noticeably improved. Our study demonstrates that lipid-derived free radical formation is mediated by NADPH-oxidase and xanthine-oxidase activation and that metal-catalysed hydroxyl radical-like species play important roles in lung injury caused by Pseudomonas aeruginosa.
引用
收藏
页码:645 / 655
页数:11
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