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Therapeutic Advances in Respiratory Disease
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Article

Erdosteine enhances airway response to salbutamol in patients with mild-to-moderate COPD

R W Dal Negro1*, Maria Visconti2, Fiorenza Trevisan2, Stefano Bertacco2, Claudio Micheletto2, and Silvia Tognella2

1 Lung Department, Orlandi General Hospital, Bussolengo, Verona, Italy
2 Orlandi General Hospital, UOC Pneumologia

* To whom correspondence should be addressed.


   Abstract

Background: Oxidative stress is presumed to impair {beta}-adenoceptor function and airway patency. Erdosteine (E), a mucomodulatory compound, has shown important antioxidant properties.

Methods: The objective was to assess the effect of antioxidant interventions on short-term airway response to salbutamol in non-reversible mild-to-moderate COPD patients. Thirty COPD patients (GOLD class 1–2), current smoker (≥10 pack/year), randomly received E 300 mg, N-acetylcysteine (NAC) 600 mg, or placebo, twice daily for ten days. Reversibility to salbutamol 200 µg was tested in baseline, after four and ten days of each treatment. ROS and 8-isoprostane blood levels were measured on the same days. Between-treatment comparison was performed by ANOVA and t-test or Wilcoxon test, and p < 0.05 assumed. E enhanced FEV1 reversibility after four and ten days significantly (+5.1% and +5.0%; both p < 0.01 vs. placebo), while NAC only showed a transient effect at day 4 (+3.0%, p < 0.05), but not at day 10 (+1.3%, p = ns).

Results: E and NAC caused significant drops in ROS blood levels after four and ten days (p < 0.001 and p < 0.0001 vs. placebo). In contrast to NAC, E lowered 8-isoprostane levels substantially for ten days (p = 0.017 and p = 0.0004 vs. placebo, respectively). Only E restored significantly short-term reversibility in COPD patients previously unresponsive to {beta}2-adrenergics.

Conclusions: This effect seems more related to the peculiar protection against lipid peroxidation rather than to the scavenging activity, which proves equal to that of NAC. E provides a sort of indirect bronchodilation through 're-sensitisation' of {beta}2-adrenoceptors. Once confirmed in further controlled studies, it may be useful in long-term treatment of COPD.

Key Words: antioxidants, b2-adrenoceptors, COPD (chronic obstructive pulmonary disease), mucolytics, lipid peroxidation, reversibility test

First published on September 3, 2008, doi:10.1177/1753465808096109

Therapeutic Advances in Respiratory Disease 2008;2:271.

A more recent version of this article appeared on October 1, 2008


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