Nitric oxide-related products and myeloperoxidase in bronchoalveolar lavage fluids from patients with ALI activate NF-kappa B in alveolar cells and monocytes

被引:17
作者
Nys, A
Preiser, JC
Deby-Dupont, G
Habraken, Y
Mathy-Hartert, A
Damas, P
Lamy, A
机构
[1] Univ Hosp Liege, Dept Anesthesia & Intens Care Med, Liege, Belgium
[2] Univ Liege, Ctr Oxygen Res & Dev, Liege, Belgium
[3] Univ Liege, Lab Fundamental Virol, Liege, Belgium
关键词
intensive care; bronchoalveolar lavage; neutrophils; reactive oxygen species; peroxynitrite; transcription factor;
D O I
10.1016/j.vph.2005.08.007
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
An increased production of NO. and peroxynitrite in lungs has been suspected during acute lung injury (ALI) in humans, and recent studies provided evidence for an alveolar production of nitrated compounds. We observed increased concentrations of nitrites/nitrates, nitrated proteins and markers of neutrophil degranulation (myeloperoxidase, elastase and lactoferrine) in the fluids recovered from bronchoalveolar lavage fluids (BALF) of patients with ALI and correlated these changes to the number of neutrophils and the severity of the ALI. We also observed that BALFs stimulated the DNA-binding activity of the nuclear transcription factor kappa B (NF-kappa B) as detected by electrophoretic mobility shift assay in human alveolar cells (A549) and monocytes (THP1). The level of activation of the NF-kappa B-binding activity was correlated to the concentration of nitrated proteins and myeloperoxidase. Furthermore, in vitro studies confirmed that NO.-derived species (peroxynitrite and nitrites) and the neutrophil enzyme myeloperoxidase by themselves increased the activation of NF-kappa B, thereby arguing for an in vivo pathogenetic role of NO.-related products and neutrophil enzymes to human ALI. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:425 / 433
页数:9
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