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

被引:39
|
作者
Aimbire, F
Albertine, R
de Magalhaes, RG
Lopes-Martins, RAB
Castro-Faria-Neto, HC
Zângaro, RA
Chavantes, MC
Pacheco, MTT
机构
[1] Univ Vale Paraiba, Inst Pesquisa & Desenvolvimento, Farmacol Lab, BR-12240000 Sao Jose Dos Campos, SP, Brazil
[2] Univ Vale Paraiba, Inst Pesquisa & Desenvolvimento, LASER, BR-12240000 Sao Jose Dos Campos, SP, Brazil
[3] Fiocruz MS, Inst Oswaldo Cruz, Lab Fisiol & Farmacodinam, BR-21045900 Rio De Janeiro, Brazil
[4] Inst Coracao, Dept Laser Biomed, Sao Paulo, Brazil
关键词
lung; hyperreactivity; low level laser therapy; LPS; prostanoids;
D O I
10.1007/s10103-005-0339-9
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
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/cm(2), 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 PGE(2) and TXA(2) 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.
引用
收藏
页码:11 / 20
页数:10
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