Effect of LLLT Ga–Al–As (685 nm) on LPS-induced inflammation of the airway and lung in the rat

被引:0
|
作者
F. Aimbire
R. Albertine
R. G. de. Magalhães
R. A. B. Lopes-Martins
H. C. Castro-Faria-Neto
R. A. Zângaro
M. C. Chavantes
M. T. T. Pacheco
机构
[1] Universidade do Vale do Paraíba Av: Shishima Hifumi,Laboratório de Farmacologia e LASER, Instituto de Pesquisa & Desenvolvimento
[2] Instituto Oswaldo Cruz,Laboratório de Fisiologia e Farmacodinâmica
[3] FIOCRUZ,Departamento de Laser em Biomedicina
[4] Instituto do Coração,undefined
来源
Lasers in Medical Science | 2005年 / 20卷
关键词
Lung; Hyperreactivity; Low level laser therapy; LPS; Prostanoids;
D O I
暂无
中图分类号
学科分类号
摘要
The purpose of this study was to investigate the effect of low level laser therapy (LLLT) on male Wistar rat trachea hyperreactivity (RTHR), bronchoalveolar lavage (BAL) and lung neutrophils influx after Gram-negative bacterial lipopolyssacharide (LPS) intravenous injection. The RTHR, BAL and lung neutrophils influx were measured over different intervals of time (90 min, 6 h, 24 h and 48 h). The energy density (ED) that produced an anti-inflammatory effect was 2.5 J/cm2, reducing the maximal contractile response and the sensibility of trachea rings to methacholine after LPS. The same ED produced an anti-inflammatory effect on BAL and lung neutrophils influx. The Celecoxib COX-2 inhibitor reduced RTHR and the number of cells in BAL and lung neutrophils influx of rats treated with LPS. Celecoxib and LLLT reduced the PGE2 and TXA2 levels in the BAL of LPS-treated rats. Our results demonstrate that LLLT produced anti-inflammatory effects on RTHR, BAL and lung neutrophils influx in association with inhibition of COX-2-derived metabolites.
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页码:11 / 20
页数:9
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