Version 1
: Received: 24 October 2016 / Approved: 24 October 2016 / Online: 24 October 2016 (05:50:30 CEST)
How to cite:
Tsai, M.-K.; Lin, Y.-C.; Lin, C.-H.; Huang, M.-Y.; Lee, M.-S.; Kuo, C.-H.; Hung, C.-H.; Kuo, P.-L. The Effects of Asthma Medications on Reactive Oxygen Species Production in Human Monocytes. Preprints2016, 2016100101. https://doi.org/10.20944/preprints201610.0101.v1
Tsai, M.-K.; Lin, Y.-C.; Lin, C.-H.; Huang, M.-Y.; Lee, M.-S.; Kuo, C.-H.; Hung, C.-H.; Kuo, P.-L. The Effects of Asthma Medications on Reactive Oxygen Species Production in Human Monocytes. Preprints 2016, 2016100101. https://doi.org/10.20944/preprints201610.0101.v1
Tsai, M.-K.; Lin, Y.-C.; Lin, C.-H.; Huang, M.-Y.; Lee, M.-S.; Kuo, C.-H.; Hung, C.-H.; Kuo, P.-L. The Effects of Asthma Medications on Reactive Oxygen Species Production in Human Monocytes. Preprints2016, 2016100101. https://doi.org/10.20944/preprints201610.0101.v1
APA Style
Tsai, M. K., Lin, Y. C., Lin, C. H., Huang, M. Y., Lee, M. S., Kuo, C. H., Hung, C. H., & Kuo, P. L. (2016). The Effects of Asthma Medications on Reactive Oxygen Species Production in Human Monocytes. Preprints. https://doi.org/10.20944/preprints201610.0101.v1
Chicago/Turabian Style
Tsai, M., Chih-Hsing Hung and Po-Lin Kuo. 2016 "The Effects of Asthma Medications on Reactive Oxygen Species Production in Human Monocytes" Preprints. https://doi.org/10.20944/preprints201610.0101.v1
Abstract
Asthma is a chronic inflammatory airway disease induced by many environmental factors. The inhalation of allergens and pollutants promote the reactive oxygen species (ROS) production leading to airway inflammation, hyper-responsiveness and remodeling in allergic asthma. The effects of asthma medications on ROS production are unclear. The present study investigated the anti-ROS effects of current asthma medications including inhaled corticosteroid (ICS; budesonide and fluticasone), leukotriene receptor antagonist (LTRA; montelukast), long acting β2 agonists (LABAs; salmeterol and formoterol) and a new extra-LABA (indacaterol). The human monocyte cell line THP-1 cells were pre-treated with different concentrations of the asthma medications at different time-points after hydrogen peroxide (H2O2) stimulation. H2O2production was measured with DCFH-DA by flow cytometry. Montelukast, fluticasone and salmeterol suppressed H2O2-induced ROS production. Indacaterol enhanced H2O2-induced ROS production. Budesonide and formoterol alone had no anti-ROS effects, but the combination of these two drugs significantly suppressed H2O2-induced ROS production. Different asthma medications have different anti-ROS effects on monocytes. The combination therapy with LABA and ICS seemed not be the only choice for asthma control. Montelukast may be also a good supplemental treatment for the poorly-controlled asthma because of its powerful anti-ROS effects. Our findings provide a novel therapeutic view in asthma.
Biology and Life Sciences, Immunology and Microbiology
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.