Oxidative stress modulates theophylline effects on steroid responsiveness.

Biochem Biophys Res Commun

National Heart & Lung Institute, Airways Disease Section, Imperial College London, Guy-Scadding Building, Dovehouse Steet, London SW3 6LY, UK.

Published: December 2008

AI Article Synopsis

  • Oxidative stress makes it harder for certain medicines to work in chronic illnesses like asthma and COPD.
  • A low level of a substance called theophylline can help these medicines work better in cells that are stressed by oxidation.
  • The study shows that theophylline changes how genes act in both normal and stressed cells, which might help improve the effects of anti-inflammatory medicines.

Article Abstract

Oxidative stress is a central factor in many chronic inflammatory diseases such as severe asthma and chronic obstructive pulmonary disease (COPD). Oxidative stress reduces the anti-inflammatory corticosteroid action and may therefore contribute to the relative corticosteroid insensitivity seen in these diseases. Low concentrations of theophylline can restore the anti-inflammatory action of corticosteroids in oxidant exposed cells, however the mechanism remains unknown. Here, we demonstrate that a low concentration of theophylline restores corticosteroid repression of pro-inflammatory mediator release and histone acetylation in oxidant exposed cells. Global gene expression analysis shows that theophylline regulates distinct pathways in naïve and oxidant exposed cells and reverses oxidant mediated modulated of pathways. Furthermore, quantitative chemoproteomics revealed that theophylline has few high affinity targets in naive cells but an elevated affinity in oxidant stressed cells. In conclusion, oxidative stress alters theophylline binding profile and gene expression which may result in restoration of corticosteroid function.

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Source
http://dx.doi.org/10.1016/j.bbrc.2008.10.065DOI Listing

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