Effect of beta2-adrenergic agonists on eosinophil adhesion, superoxide anion generation, and degranulation

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Abstract

Background Eosinophils play important roles in the development of asthma exacerbation. Viral infection is a major cause of asthma exacerbation, and the expression of IFN-γ-inducible protein of 10 kDa (IP-10) and cysteinyl leukotrienes (cysLTs) is up-regulated in virus-induced asthma. As β2-adrenergic agonists, such as formoterol or salbutamol, are used to treat asthma exacerbation, we examined whether formoterol or salbutamol could modify eosinophil functions such as adhesiveness, particularly those activated by cysLTs or IP-10. Methods Eosinophils were isolated from the blood of healthy subjects and were pre-incubated with either formoterol or salbutamol, and subsequently stimulated with IL-5, LTD<inf>4</inf>, or IP-10. Adhesion of eosinophils to intercellular cell adhesion molecule (ICAM)-1 was measured using eosinophil peroxidase assays. The generation of eosinophil superoxide anion (O<inf>2</inf><sup>-</sup>) was examined based on the superoxide dismutase-inhibitable reduction of cytochrome C. Eosinophil-derived neurotoxin (EDN) release was evaluated by ELISA as a marker of degranulation. Results Neither formoterol nor salbutamol suppressed the spontaneous adhesion of eosinophils to ICAM-1. However, when eosinophils were activated by IL-5, LTD<inf>4</inf>, or IP-10, formoterol, but not salbutamol, suppressed the adhesion to ICAM-1. Formoterol also suppressed IL-5, LTD<inf>4</inf>, or IP-10 induced eosinophil O<inf>2</inf><sup>-</sup> generation or EDN release. Conclusions These findings suggest that formoterol, but not salbutamol, suppresses eosinophil functions enhanced by IL-5, LTD<inf>4</inf>, or IP-10. As these factors are involved in the development of asthma exacerbation, our results strongly support the hypothesis that administration of formoterol is a novel strategy for treating asthma exacerbation.

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APA

Noguchi, T., Nakagome, K., Kobayashi, T., Ueda, Y., Soma, T., Nakamoto, H., & Nagata, M. (2015). Effect of beta2-adrenergic agonists on eosinophil adhesion, superoxide anion generation, and degranulation. Allergology International, 64, S46–S53. https://doi.org/10.1016/j.alit.2015.05.009

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