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

机译:暴露于铜绿假单胞菌细菌后小鼠肺中自由基生成的体内证据:ESR自旋捕获研究

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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 α-(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 Hβ =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.
机译:在铜绿假单胞菌诱导的啮齿动物性肺炎模型中,认为自由基与疾病发病机理显着相关。但是,到目前为止,还没有直接证据表明体内存在自由基。在这里,我们使用电子自旋共振(ESR)和与α-(4-吡啶基-1-氧化物)-N-叔丁基硝酮的体内自旋捕获来研究小鼠模型中自由基的产生。我们检测并鉴定了体内脂质衍生的自由基的产生(N = 14.86±0.03 G和Hβ= 2.48±0.09 G)。为了进一步研究脂质自由基产生的机制,我们使用了调节剂和敲除小鼠。我们发现,使用GdCl3(吞噬性有毒物),NADPH-氧化酶敲除小鼠(Nox2-/-),别嘌呤醇(黄嘌呤氧化酶抑制剂)和Desferal(金属螯合剂)时,脂质自由基的产生减少了。急性肺损伤的组织病理学和生物学指标明显改善。我们的研究表明,脂质衍生的自由基形成是由NADPH-氧化酶和黄嘌呤氧化酶激活介导的,并且金属催化的羟基自由基样物质在铜绿假单胞菌引起的肺损伤中起重要作用。

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