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内毒素诱导的针对金黄色葡萄球菌的肺部抗菌防御抑制。

Endotoxin-induced suppression of pulmonary antibacterial defenses against Staphylococcus aureus.

作者信息

Harris S E, Nelson S, Astry C L, Bainton B G, Summer W R

机构信息

Department of Pulmonary/Critical Care Medicine, Louisiana State University Medical Center, New Orleans 70112.

出版信息

Am Rev Respir Dis. 1988 Dec;138(6):1439-43. doi: 10.1164/ajrccm/138.6.1439.

DOI:10.1164/ajrccm/138.6.1439
PMID:3059896
Abstract

In order to evaluate the effect of endotoxin on lung host defenses, Sprague-Dawley rats were intravenously injected with either placebo or 5 mg/kg of Escherichia coli lipopolysaccharide B. Two hours after treatment, animals were challenged with Staphylococcus aureus by either low dose aerosol inhalation or high dose intratracheal instillation of the bacteria into the lungs. Quantitative lung bacteriologic examination and bronchoalveolar lavage (BAL) for total and differential cell counts were performed immediately (zero hour) and at 4 h after bacterial challenge. Lung phagocytic defenses against aerosolized S. aureus challenges are provided solely by the alveolar macrophage (AM) in the absence of inflammation. In aerosol-challenged control rats, 20.6 +/- 2.0% of the initial deposited bacterial challenge remained viable in the lung at 4 h. Animals pretreated with endotoxin, however, showed a significant decrease in pulmonary bactericidal activity (31.3 +/- 3.4% bacteria remaining at 4 h), indicating a defect in alveolar macrophage (AM) function. Further assessment of the bactericidal oxidative metabolism of endotoxin-treated AM by luminol-enhanced chemiluminescence indicated an increased production of free radical oxygen species when compared with control nontreated cells in both the unstimulated (66 +/- 4 versus 38 +/- 7 x 10(3) cpm in control) and stimulated (250.5 +/- 17.1 versus 147.1 +/- 6.2 x 10(3) cpm in control) states. Total and differential cell counts in both control and endotoxin-treated aerosol-challenged rats were similar.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了评估内毒素对肺部宿主防御功能的影响,将Sprague-Dawley大鼠静脉注射安慰剂或5mg/kg的大肠杆菌脂多糖B。治疗两小时后,通过低剂量气溶胶吸入或高剂量气管内注入金黄色葡萄球菌对动物进行攻击。在细菌攻击后立即(零小时)和4小时进行肺部细菌定量检查以及支气管肺泡灌洗(BAL)以进行总细胞计数和分类细胞计数。在没有炎症的情况下,肺部对雾化金黄色葡萄球菌攻击的吞噬防御仅由肺泡巨噬细胞(AM)提供。在雾化攻击的对照大鼠中,初始沉积的细菌攻击中有20.6±2.0%在4小时时在肺部仍存活。然而,用内毒素预处理的动物肺部杀菌活性显著降低(4小时时剩余31.3±3.4%的细菌),表明肺泡巨噬细胞(AM)功能存在缺陷。通过鲁米诺增强化学发光对经内毒素处理的AM的杀菌氧化代谢进行进一步评估表明,与未处理的对照细胞相比,在未刺激状态(对照中为66±4对38±7 x 10(3) cpm)和刺激状态(对照中为250.5±17.1对147.1±6.2 x 10(3) cpm)下,自由基氧物种的产生均增加。对照和经内毒素处理的雾化攻击大鼠中的总细胞计数和分类细胞计数相似。(摘要截断于250字)

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