Abstract

BackgroundAllergic asthma is an inflammatory disease resulting from continued or intermittent allergen exposure, and allergic rhinitis can be trigger of asthma. The main mechanism of these disease is allergic reaction and immune response dysregulation. Co-Q10 is an enzyme cofactor in mitochondria can control asthma and allergic rhinitis symptoms. In the present study, we determined that the CoQ10-induced anti-allergic effects were mediated by up-regulation of Nrf2.MethodsAnimal models of allergic rhinitis and allergic asthma were produced and treated with Co-Q10, Co-Q10 and O-3, Co-Q10 and Mg-S. Bronchoalveolar lavage fluid was collected from animal models, and IL-4, 5, 13, INF-y, Eicosanoids, IgE, EPO, and histamine production were measured. Also, COX-2, CCL24, CCL11, Nrf2, Eotaxin, Cytb, COX1 and ND1 genes expressions and histopathology were studied. BALf's cells were collected by tracheostomy and used in slide producing by cytospine. Cytokines, Eicosanoids, IgE, EPO, and histamine were measured by ELISA method. Gene expression was done by Real-time PCR.ResultsCo-Q10 with two supplementation (Mg-S and O-3) modulate MRC, BALf eosinophils, eosinophilic inflammation related genes (eotaxin, CCL11 and CCL24), peribronchial and perivascular inflammation, EPO, type 2 cytokines (IL-4, 5 and 13), IgE, histamine, Cyc-LT and LTB4 as main allergic bio-factors. Importantly, Co-Q10 treatment increased Nrf2 expression and Nrf2 induced antioxidant genes, glutathione redox and inhibited inflammation, oxidative stress injury, Th2 cytokines production and attenuated allergic inflammatory responses.ConclusionNrf2 is activated in response to allergen, induces resistance against the rhinitis and asthma development and plays an essential role in broncho-protection. Co-Q10 increases the Nrf2 expression and the Nrf2 over-expression has strong effect in control of type2 cytokines, allergic mediators and inflammatory factors that lead to harnessing of allergy and asthma.Graphic abstract

Highlights

  • Asthma is a complex chronic inflammatory disease of the bronchi

  • It is recognized that asthma is a chronic inflammatory disease resulting from continued or intermittent allergen exposure, and allergic rhinitis can be trigger of asthma

  • The eosinophil percentage were significantly decreased by three treatment (Co-Q10: 38 ± 5%, Co-Q10, O-3: 28 ± 9%, Co-Q10, Magnesium sulfate (Mg-S): 37 ± 2%) on day 31 compared to non-treated asthmatic group (P < 0.05) (Fig. 2)

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Summary

Introduction

Asthma is a complex chronic inflammatory disease of the bronchi. It is recognized that asthma is a chronic inflammatory disease resulting from continued or intermittent allergen exposure, and allergic rhinitis can be trigger of asthma. The most common allergic diseases include allergic rhinitis, conjunctivitis, allergic asthma, atopic dermatitis, food allergy, and anaphylaxis. Allergic asthma is an inflammatory disease resulting from continued or intermittent allergen exposure, and allergic rhinitis can be trigger of asthma. The main mechanism of these disease is allergic reaction and immune response dysregulation. Co-Q10 is an enzyme cofactor in mitochondria can control asthma and allergic rhinitis symptoms. We determined that the CoQ10-induced anti-allergic effects were mediated by up-regulation of Nrf

Methods
Results
Conclusion
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