Volume 43, Issue 9 pp. 1071-1082
Original Article

MAG-EPA resolves lung inflammation in an allergic model of asthma

C. Morin

C. Morin

SCF Pharma, Ste-Luce, QC, Canada

Department of Physiology and Biophysics, Faculty of Medicine and Health Sciences, Sherbrooke, QC, Canada

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S. Fortin

S. Fortin

SCF Pharma, Ste-Luce, QC, Canada

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A. M. Cantin

A. M. Cantin

Department of Medicine, Respiratory Division, Université de Sherbrooke, Sherbrooke, QC, Canada

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É. Rousseau

Corresponding Author

É. Rousseau

Department of Physiology and Biophysics, Faculty of Medicine and Health Sciences, Sherbrooke, QC, Canada

Correspondence: Dr Éric Rousseau, Department of Physiology and Biophysics, Faculty of Medicine and Health Sciences, Université de Sherbrooke, 3001, 12th Avenue North, Sherbrooke, QC, Canada J1H 5N4.

E-mail: [email protected]

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First published: 22 June 2013
Citations: 31

Summary

Background

Asthma is a chronic disease characterized by airways hyperresponsiveness, inflammation and airways remodelling involving reversible bronchial obstruction. Omega-3 fatty acids and their derivatives are known to reduce inflammation in several tissues including lung.

Objectives

The effects of eicosapentaenoic acid monoacylglyceride (MAG-EPA), a newly synthesized EPA derivative, were determined on the resolution of lung inflammation and airway hyperresponsiveness in an in vivo model of allergic asthma.

Methods

Ovalbumin (OVA)-sensitized guinea-pigs were treated or not with MAG-EPA administered per os. Isometric tension measurements, histological analyses, homogenate preparation for Western blot experiments or total RNA extraction for RT-PCR were performed to assess the effect of MAG-EPA treatments.

Results

Mechanical tension measurements revealed that oral MAG-EPA treatments reduced methacholine (MCh)-induced bronchial hyperresponsiveness in OVA-sensitized guinea-pigs. Moreover, MAG-EPA treatments also decreased Ca2+ hypersensitivity of bronchial smooth muscle. Histological analyses and leucocyte counts in bronchoalveolar lavages revealed that oral MAG-EPA treatments led to less inflammatory cell recruitment in the lung of OVA-sensitized guinea-pigs when compared with lungs from control animals. Results also revealed a reduction in mucin production and MUC5AC expression level in OVA-sensitized animals treated with MAG-EPA. Following MAG-EPA treatments, the transcript levels of pro-inflammatory markers such as IL-5, eotaxin, IL-13 and IL-4 were markedly reduced. Moreover, per os MAG-EPA administrations reduced COX2 over-expression in OVA-sensitized animals.

Conclusion and Clinical Relevance

We demonstrate that MAG-EPA reduces airway hyperresponsiveness and lung inflammation in OVA-sensitized animals, a finding consistent with a decrease in IL-4, IL-5, IL-13, COX-2 and MUC5AC expression levels in the lung. The present data suggest that MAG-EPA represents a new potential therapeutic strategy for resolving inflammation in allergic asthma.

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