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脂质X可改善肺动脉高压,并保护绵羊免于因内毒素导致死亡。

Lipid X ameliorates pulmonary hypertension and protects sheep from death due to endotoxin.

作者信息

Golenbock D T, Will J A, Raetz C R, Proctor R A

机构信息

Department of Medicine, University of Wisconsin, Madison 53706.

出版信息

Infect Immun. 1987 Oct;55(10):2471-6. doi: 10.1128/iai.55.10.2471-2476.1987.

Abstract

Lipid X (2,3-diacylglucosamine-1-phosphate) is a novel monosaccharide precursor of lipid A that has some of the physiologic activities of endotoxin but little toxicity. To determine whether lipid X would interfere with the toxic effects of endotoxin, we pretreated sheep with either 100 or 200 micrograms of lipid X per kg of body weight and then challenged them with a potentially fatal dose of Escherichia coli endotoxin (20 micrograms/kg). Twenty-one sheep underwent pulmonary artery catheterization and were monitored for changes in pulmonary artery pressure, temperature, pH, partial O2 pressure, partial CO2 pressure, blood pressure, and cell counts over 7 h. Overall mortality for control animals was 37% versus 5.3% for pretreated animals. None of the 13 animals pretreated with 100 micrograms of lipid X per kg died. These differences in survival were significant (P less than 0.05). Animals pretreated with 100 micrograms of lipid X per kg had significantly lower pulmonary artery pressure during both phases 1 and 2 of endotoxin-induced pulmonary artery hypertension. A higher dose of lipid X, 200 micrograms/kg, produced pulmonary hypertension. Perhaps because lipid X is a subunit of lipid A, lipid X shows a partial pyrogenic effect while also decreasing the pyrogenic activity of complete lipopolysaccharide (LPS). Lipid X did not prevent endotoxin-induced neutropenia or moderate hypotension in response to LPS. Lipid X is a potential prototype compound for a new type of chemotherapy directed at blocking the harmful effects of LPS during bacterial septicemia.

摘要

脂质X(2,3 - 二酰基葡糖胺 - 1 - 磷酸)是一种新型的脂质A单糖前体,具有内毒素的一些生理活性,但毒性很小。为了确定脂质X是否会干扰内毒素的毒性作用,我们以每千克体重100或200微克的脂质X预处理绵羊,然后用潜在致命剂量的大肠杆菌内毒素(20微克/千克)对其进行攻击。21只绵羊接受了肺动脉插管,并在7小时内监测肺动脉压力、体温、pH值、氧分压、二氧化碳分压、血压和细胞计数的变化。对照动物的总体死亡率为37%,而预处理动物为5.3%。每千克体重用100微克脂质X预处理的13只动物中无一死亡。这些生存差异具有显著性(P小于0.05)。每千克体重用100微克脂质X预处理的动物在内毒素诱导的肺动脉高压的第1和第2阶段肺动脉压力均显著较低。更高剂量的脂质X,即200微克/千克,会导致肺动脉高压。也许因为脂质X是脂质A的一个亚基,脂质X显示出部分致热作用,同时也降低了完整脂多糖(LPS)的致热活性。脂质X不能预防内毒素诱导的中性粒细胞减少或对LPS的中度低血压反应。脂质X是一种潜在的原型化合物,可用于一种新型化疗,旨在在细菌性败血症期间阻断LPS的有害作用。

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