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低剂量大肠杆菌溶血素诱导兔肺产生白三烯和羟基二十碳四烯酸

Leukotriene and hydroxyeicosatetraenoic acid generation elicited by low doses of Escherichia coli hemolysin in rabbit lungs.

作者信息

Grimminger F, Walmrath D, Birkemeyer R G, Bhakdi S, Seeger W

机构信息

Department of Internal Medicine, Justus-Liebig-University, Giessen, Federal Republic of Germany.

出版信息

Infect Immun. 1990 Aug;58(8):2659-63. doi: 10.1128/iai.58.8.2659-2663.1990.

DOI:10.1128/iai.58.8.2659-2663.1990
PMID:2115026
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC258869/
Abstract

Low doses of Escherichia coli hemolysin cause thromboxane-mediated hypertension and vascular leakage in blood-free perfused rabbit lungs (W. Seeger, H. Walter, N. Suttorp, M. Muhly, and S. Bhakdi, J. Clin. Invest. 84:220-227, 1989). The recirculating buffer medium and bronchoalveolar lavage fluid from lungs exposed to hemolysin (2.5 hemolytic units per ml) in the presence of cyclooxygenase inhibitor were analyzed for leukotrienes (LTs) and hydroxyeicosatetraenoic acids (HETEs) by reverse-phase and straight-phase high-pressure liquid chromatographic techniques combined with UV spectrum analysis and post-high-pressure liquid chromatography radioimmunoassay. A rapid release of large amounts of cysteinyl-LTs and leukotriene B4 (LTB4) into the intravascular space was noted (total sum, approximately 4 to 5 micrograms). Similar quantities have hitherto been elicited only by high concentrations of the artificial calcium ionophore A 23187. Moreover, a marked liberation of 5-HETE and 12-hydroxyheptadecatrienoic acid into the buffer medium occurred, whereas LTB4 represented the predominant compound in the lavage fluid. The hemolysin-induced burst of LT and HETE generation preceded the onset of vascular leakage. The outstanding capacity of E. coli hemolysin to produce the liberation of potent lipid mediators is probably relevant to the pathways of vascular injury and amplification of inflammatory events during severe infection with hemolytic E. coli strains.

摘要

低剂量的大肠杆菌溶血素可导致无血灌注兔肺中血栓素介导的高血压和血管渗漏(W. 西格、H. 瓦尔特、N. 苏托普、M. 穆利和S. 巴克迪,《临床研究杂志》84:220 - 227,1989年)。采用反相和正相高压液相色谱技术结合紫外光谱分析及高压液相色谱后放射免疫测定法,对在环氧化酶抑制剂存在的情况下暴露于溶血素(每毫升2.5个溶血单位)的肺的再循环缓冲介质和支气管肺泡灌洗液中的白三烯(LTs)和羟基二十碳四烯酸(HETEs)进行了分析。结果发现大量的半胱氨酰白三烯和白三烯B4(LTB4)迅速释放到血管内空间(总量约为4至5微克)。迄今为止,只有高浓度的人工钙离子载体A 23187才能引发类似数量的释放。此外,5 - HETE和12 - 羟基十七碳三烯酸大量释放到缓冲介质中,而LTB4是灌洗液中的主要化合物。溶血素诱导的LT和HETE生成爆发先于血管渗漏的发生。大肠杆菌溶血素产生强效脂质介质释放的显著能力可能与溶血性大肠杆菌菌株严重感染期间的血管损伤途径和炎症事件放大有关。

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