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本文引用的文献

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Elevated thromboxane levels in the rat during endotoxic shock: protective effects of imidazole, 13-azaprostanoic acid, or essential fatty acid deficiency.内毒素休克期间大鼠血栓素水平升高:咪唑、13-氮杂前列腺酸或必需脂肪酸缺乏的保护作用。
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Induction of immunity against lethal Haemophilus influenzae type b infection by Escherichia coli core lipopolysaccharide.大肠杆菌核心脂多糖诱导针对致死性b型流感嗜血杆菌感染的免疫
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Effectiveness of steroid/antibiotic treatment in primates administered LD100 Escherichia coli.类固醇/抗生素治疗对接受致死剂量100的大肠杆菌的灵长类动物的有效性。
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Lung injury and lung lysosomal enzyme release during endotoxemia.内毒素血症期间的肺损伤和肺溶酶体酶释放。
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Two interacting mutations causing temperature-sensitive phosphatidylglycerol synthesis in Escherichia coli membranes.两个相互作用的突变导致大肠杆菌细胞膜中温度敏感型磷脂酰甘油的合成。
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Endotoxic immunity.内毒素免疫
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Treatment of gram-negative bacteremia and shock with human antiserum to a mutant Escherichia coli.用人抗突变型大肠杆菌抗血清治疗革兰氏阴性菌血症和休克。
N Engl J Med. 1982 Nov 11;307(20):1225-30. doi: 10.1056/NEJM198211113072001.
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Immunobiologically active lipid A analogs synthesized according to a revised structural model of natural lipid A.根据天然脂质A的修订结构模型合成的具有免疫生物学活性的脂质A类似物。
Infect Immun. 1984 Jul;45(1):293-6. doi: 10.1128/iai.45.1.293-296.1984.
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Biological activities of synthetic lipid A analogs: pyrogenicity, lethal toxicity, anticomplement activity, and induction of gelation of Limulus amoebocyte lysate.合成脂多糖A类似物的生物学活性:致热性、致死毒性、抗补体活性及鲎试剂凝胶化诱导作用。
Infect Immun. 1984 May;44(2):421-6. doi: 10.1128/iai.44.2.421-426.1984.
10
Influence of fine structure of lipid A on Limulus amebocyte lysate clotting and toxic activities.脂多糖A的精细结构对鲎试剂凝血及毒性活性的影响。
Infect Immun. 1984 Aug;45(2):350-5. doi: 10.1128/iai.45.2.350-355.1984.

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.

DOI:10.1128/iai.55.10.2471-2476.1987
PMID:3308707
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC260732/
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。