Low Level Laser Therapy Reduces the Development of Lung Inflammation Induced by Formaldehyde Exposure

被引:48
作者
da Silva, Cristiane Miranda [1 ]
Leal, Mayara Peres [1 ]
Brochetti, Robson Alexandre [1 ]
Braga, Tarcio [2 ]
Vitoretti, Luana Beatriz [1 ]
Saraiva Camara, Niels Olsen [2 ]
Damazo, Amilcar Sabino [3 ]
Ligeiro-de-Oliveira, Ana Paula [1 ]
Chavantes, Maria Cristina [4 ]
Lino-dos-Santos-Franco, Adriana [1 ]
机构
[1] Univ Nove de Julho UNINOVE, Post Grad Program Biophoton Appl Hlth Sci, Sao Paulo, Brazil
[2] Univ Sao Paulo, Dept Immunol, Sao Paulo, Brazil
[3] Fed Univ Cuiaba, Dept Basic Sci Hlth, Fac Med Sci, Cuiaba, Brazil
[4] Univ Nove de Julho UNINOVE, Post Grad Program Med, Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
ALLERGIC-ASTHMA; MAST-CELLS; RAT MODEL; LLLT; GRANULOPOIESIS; NEUTROPHILS; PRODUCTS; RELEASE; MARROW; TISSUE;
D O I
10.1371/journal.pone.0142816
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lung diseases constitute an important public health problem and its growing level of concern has led to efforts for the development of new therapies, particularly for the control of lung inflammation. Low Level Laser Therapy (LLLT) has been highlighted as a non-invasive therapy with few side effects, but its mechanisms need to be better understood and explored. Considering that pollution causes several harmful effects on human health, including lung inflammation, in this study, we have used formaldehyde (FA), an environmental and occupational pollutant, for the induction of neutrophilic lung inflammation. Our objective was to investigate the local and systemic effects of LLLT after FA exposure. Male Wistar rats were exposed to FA (1%) or vehicle (distillated water) during 3 consecutive days and treated or not with LLLT (1 and 5 hours after each FA exposure). Non-manipulated rats were used as control. 24 h after the last FA exposure, we analyzed the local and systemic effects of LLLT. The treatment with LLLT reduced the development of neutrophilic lung inflammation induced by FA, as observed by the reduced number of leukocytes, mast cells degranulated, and a decreased myeloperoxidase activity in the lung. Moreover, LLLT also reduced the microvascular lung permeability in the parenchyma and the intrapulmonary bronchi. Alterations on the profile of inflammatory cytokines were evidenced by the reduced levels of IL-6 and TNF-alpha and the elevated levels of IL-10 in the lung. Together, our results showed that LLLT abolishes FA-induced neutrophilic lung inflammation by a reduction of the inflammatory cytokines and mast cell degranulation. This study may provide important information about the mechanisms of LLLT in lung inflammation induced by a pollutant.
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页数:16
相关论文
共 34 条
[1]   Low-level laser therapy can reduce lipopolysaccharide-induced contractile force dysfunction and TNF-α levels in rat diaphragm muscle [J].
Aimbire, F. ;
Lopes-Martins, R. A. B. ;
Castro-Faria-Neto, H. C. ;
Albertini, R. ;
Chavantes, M. C. ;
Pacheco, M. T. T. ;
Leonardo, P. S. L. M. ;
Iversen, V. V. ;
Bjordal, J. M. .
LASERS IN MEDICAL SCIENCE, 2006, 21 (04) :238-244
[2]   Effect of LLLT Ga-Al-As (685 nm) on LPS-induced inflammation of the airway and lung in the rat [J].
Aimbire, F ;
Albertine, R ;
de Magalhaes, RG ;
Lopes-Martins, RAB ;
Castro-Faria-Neto, HC ;
Zângaro, RA ;
Chavantes, MC ;
Pacheco, MTT .
LASERS IN MEDICAL SCIENCE, 2005, 20 (01) :11-20
[3]  
Avci P, 2013, SEMIN CUTAN MED SURG, V32, P41
[4]   Neutrophils, from Marrow to Microbes [J].
Borregaard, Niels .
IMMUNITY, 2010, 33 (05) :657-670
[5]  
Carlson Ryan M, 2004, Dermatitis, V15, P169, DOI 10.2310/6620.2004.04021
[6]  
Chavantes M.C, 2005, PHOTOMED LASER SURG, V1, P113
[7]  
de Lima FM, 2014, J LASERS MED SCI, V5, P63
[8]   Low-level laser therapy (LLLT) acts as cAMP-elevating agent in acute respiratory distress syndrome [J].
de Lima, Flavia Mafra ;
Moreira, Leonardo M. ;
Villaverde, A. B. ;
Albertini, Regiane ;
Castro-Faria-Neto, Hugo C. ;
Aimbire, Flavio .
LASERS IN MEDICAL SCIENCE, 2011, 26 (03) :389-400
[9]   CXCR4 is a key regulator of neutrophil release from the bone marrow under basal and stress granulopoiesis conditions [J].
Eash, Kyle J. ;
Means, Jacquelyn M. ;
White, Douglas W. ;
Link, Daniel C. .
BLOOD, 2009, 113 (19) :4711-4719
[10]  
Faradzheva N A, 2007, Probl Tuberk Bolezn Legk, P50