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首页> 外文期刊>Infection and immunity >In vivo protective effect of lipopolysaccharide against Pseudomonas aeruginosa exotoxin A in mice.
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In vivo protective effect of lipopolysaccharide against Pseudomonas aeruginosa exotoxin A in mice.

机译:脂多糖对小鼠铜绿假单胞菌外毒素A的体内保护作用。

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Lipopolysaccharide (LPS) treatment of mice 1 to 5 days prior to administration of Pseudomonas aeruginosa exotoxin A (PA) induced full or partial protection against PA intoxication. The optimal LPS dose that induced resistance was 50 to 100 micrograms per mouse. Simultaneous administration of LPS and PA to mice, however, increased their sensitivity to PA two- to fourfold. Mice pretreated with LPS demonstrated a markedly enhanced clearance rate of 125I-labeled PA from peripheral blood, livers, and kidneys. In mice exposed to LPS and PA simultaneously, the rate of elimination of labeled PA was lower than that in control mice. While protein synthesis was inhibited significantly in livers and other organs of PA-exposed mice, in LPS-pretreated mice, PA-induced inhibition of protein synthesis was either diminished or totally prevented and elongation factor 2 (EF2) levels were normal. In mice treated only with LPS, enhanced protein synthesis and increased levels of EF2 were observed, suggesting that LPS protection against PA intoxication was perhaps a consequence of excessive amounts of EF2 induced by LPS.
机译:在给予铜绿假单胞菌外毒素A(PA)之前1-5天,对小鼠进行脂多糖(LPS)处理可诱导部分或全部保护免受PA中毒。诱导抗性的最佳LPS剂量为每只小鼠50至100微克。同时向小鼠施用LPS和PA,将其对PA的敏感性提高了2到4倍。用LPS预处理的小鼠表现出125I标记的PA从外周血,肝脏和肾脏的清除率显着提高。在同时暴露于LPS和PA的小鼠中,标记的PA的消除速率低于对照小鼠。虽然在PA暴露的小鼠的肝脏和其他器官中蛋白质合成受到显着抑制,但在LPS预处理的小鼠中,PA诱导的蛋白合成抑制被减弱或完全被阻止,并且伸长因子2(EF2)水平正常。在仅用LPS治疗的小鼠中,观察到蛋白质合成增强和EF2水平升高,这表明LPS对PA中毒的保护作用可能是LPS诱导的过量EF2的结果。

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