首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Efficacy of treatment with the iron (III) complex of diethylenetriamine pentaacetic acid in mice and primates inoculated with live lethal dose 100 Escherichia coli.
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Efficacy of treatment with the iron (III) complex of diethylenetriamine pentaacetic acid in mice and primates inoculated with live lethal dose 100 Escherichia coli.

机译:用二乙烯三胺五乙酸铁(III)络合物治疗活致命剂量100大肠杆菌的小鼠和灵长类动物的疗效。

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摘要

The iron (III) complex of diethylenetriamine pentaacetic acid (DTPA iron [III]) protected mice and baboons from the lethal effects of an infusion with live LD100 Escherichia coli. In mice, optimal results were obtained when DTPA iron (III) was administered two or more hours after infection. Prevention of death occurred in spite of the fact that the adverse effects of TNF-alpha were well underway in the mouse model. The half-life of DTPA iron (III) was 51 +/- 9 min in normal baboons; primary clearance was consistent with glomerular filtration. In septic baboons, survival was observed after administration of two doses of DTPA iron (III) at 2.125 mg/kg, the first one given before, or as late as 2 h after, severe hypotension. Administration of DTPA iron (III) did not alter mean systemic arterial pressure, but did protect baboons in the presence of high levels of TNF-alpha and free radical overproduction. Furthermore, exaggerated production of nitric oxide was attenuated. The mechanism of protection with DTPA iron (III) is not obvious. Because of its ability to interact in vitro with free radicals, its poor cell permeability, and its short half-life, we postulate that DTPA iron (III) and/or its reduced form may have protected the mice and baboons by sequestration and subsequent elimination of free radicals (including nitric oxide) from their systems.
机译:二亚乙基三胺五乙酸的铁(III)配合物(DTPA铁[III])保护小鼠和狒狒免受输注活LD100大肠杆菌的致死作用。在小鼠中,感染后两个小时或更长时间施用DTPA铁(III)可获得最佳结果。尽管在小鼠模型中TNF-α的不良反应正在进行中,但仍可以预防死亡。在正常狒狒中,DTPA铁(III)的半衰期为51 +/- 9分钟。主要清除率与肾小球滤过一致。在化脓性狒狒中,在以2.125 mg / kg的剂量服用两剂DTPA铁(III)后观察到存活,第一剂在严重低血压发生之前或迟于2小时出现。施用DTPA铁(III)不会改变平均全身动脉压,但是在存在高水平的TNF-α和自由基过度生产的情况下,确实可以保护狒狒。此外,一氧化氮的过量产生被减弱。 DTPA铁(III)的保护机理并不明显。由于它在体外与自由基相互作用的能力,较差的细胞通透性和较短的半衰期,我们推测DTPA铁(III)和/或其还原形式可能通过螯合和随后的消除作用保护了小鼠和狒狒系统中的自由基(包括一氧化氮)。

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