Aerobic Exercise Reduces Asthma Phenotype by Modulation of the Leukotriene Pathway

Leukotrienes (LTs) play a central role in asthma. Low- to moderate-intensity aerobic exercise (AE) reduces asthmatic inflammation in clinical studies and in experimental models. This study investigated whether AE attenuates LT pathway activation in an ovalbumin (OVA) model of asthma. Sixty-four male...

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Veröffentlicht in:Frontiers in immunology 2016-06, Vol.7, p.237-237
Hauptverfasser: Alberca-Custódio, Ricardo Wesley, Greiffo, Flávia Regina, MacKenzie, BreAnne, Oliveira-Junior, Manoel Carneiro, Andrade-Sousa, Adilson Santos, Graudenz, Gustavo Silveira, Santos, Angela Batista Gomes, Damaceno-Rodrigues, Nilsa Regina, Castro-Faria-Neto, Hugo Caire, Arantes-Costa, Fernanda Magalhaes, Martins, Milton De Arruda, Abbasi, Asghar, Lin, Chin Jia, Idzko, Marco, Ligeiro Oliveira, Ana Paula, Northoff, Hinnak, Vieira, Rodolfo Paula
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Sprache:eng
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Zusammenfassung:Leukotrienes (LTs) play a central role in asthma. Low- to moderate-intensity aerobic exercise (AE) reduces asthmatic inflammation in clinical studies and in experimental models. This study investigated whether AE attenuates LT pathway activation in an ovalbumin (OVA) model of asthma. Sixty-four male, BALB/c mice were distributed into Control, Exercise (Exe), OVA, and OVA + Exe groups. Treadmill training was performed at moderate intensity, 5×/week, 1 h/session for 4 weeks. Quantification of bronchoalveolar lavage (BAL) cellularity, leukocytes, airway remodeling, interleukin (IL)-5, IL-13, cysteinyl leukotriene (CysLT), and leukotriene B4 (LTB4) in BAL was performed. In addition, quantitative analyses on peribronchial leukocytes and airway epithelium for LT pathway agents: 5-lypoxygenase (5-LO), LTA4 hydrolase (LTA4H), CysLT1 receptor, CysLT2 receptor, LTC4 synthase, and LTB4 receptor 2 (BLT2) were performed. Airway hyperresponsiveness (AHR) to methacholine (MCh) was assessed via whole body plethysmography. AE decreased eosinophils (p  0.001), lymphocytes (p 
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2016.00237