Deferoxamine reduces tissue injury and lethality in LPS-treated mice

Marisa Vulcano , Roberto P. Meiss , Martı́n A. Isturiz
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引用次数: 53

Abstract

We studied the effect of deferoxamine (DFX), an iron chelator, which can also act as a free radical scavenger, in an experimental murine model of sepsis. In vivo studies demonstrated that pretreatment of mice with DFX reduces tumor necrosis factor alpha (TNF-α) serum levels and increases the rate of survival of mice inoculated with lethal doses of lipopolysaccharide (LPS) or Escherichia coli O111:B4. By using the iron chelated form of DFX (ferrioxamine) the same results were obtained, suggesting that in this model, DFX could act as a free radical scavenger. On the other hand, DFX prevents mortality induced either by LPS or murine recombinant TNF-α in D(+)-galactosamine (GalN)-sensitized mice. These protective actions of DFX correlate with an attenuated tissue damage observed in lungs, livers and kidneys of LPS-treated animals and GalN-sensitized mice inoculated with TNF-α.

去铁胺减少lps处理小鼠的组织损伤和致死率
我们研究了去铁胺(DFX),一种铁螯合剂,也可以作为自由基清除剂,在实验小鼠脓毒症模型中的作用。体内研究表明,DFX预处理小鼠可降低血清中肿瘤坏死因子α (TNF-α)水平,并提高小鼠接种致死剂量脂多糖(LPS)或大肠杆菌O111:B4的存活率。使用铁螯合形式的DFX(铁胺)获得了相同的结果,表明在该模型中,DFX可以作为自由基清除剂。另一方面,DFX在D(+)-半乳糖胺(GalN)致敏小鼠中可防止LPS或小鼠重组TNF-α引起的死亡。DFX的这些保护作用与lps处理动物和接种TNF-α的galn致敏小鼠的肺、肝脏和肾脏中观察到的组织损伤减弱相关。
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