4.5 Article

The effect of an oral anti-oxidant, N-Acetyl-cysteine, on inflammatory and oxidative markers in pulmonary sarcoidosis

Journal

RESPIRATORY MEDICINE
Volume 112, Issue -, Pages 106-111

Publisher

W B SAUNDERS CO LTD
DOI: 10.1016/j.rmed.2016.01.011

Keywords

Sarcoidosis; N-Acetyl-Cysteine; Oxidative stress

Funding

  1. American Thoracic Society/Foundation for Sarcoidosis Research
  2. NIH/NCATS Colorado CTSA [UL1 TR001082]

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Background: Oxidative stress (OS) has been shown to play a role in the pathogenesis of sarcoidosis and previous studies have shown that anti-oxidants can reduce markers of oxidative stress and inflammation in the peripheral blood of sarcoidosis subjects. We investigated the effect of N-Acetyl-Cysteine (NAC) on oxidative stress and inflammatory markers in the lungs of sarcoidosis patients. Methods: We randomized 11 sarcoidosis subjects to active therapy and 3 to placebo for 8 weeks in a double blinded study. Bronchoscopy with bronchoalveolar lavage was performed pre and post therapy. Our primary endpoint was TNF-alpha production from stimulated and unstimulated BAL cells. Secondary outcomes included measures of oxidative stress (GSH, 8-OHdG) levels in the BAL. In-vitro studies were also performed to assess the effect of NAC on lipopolysaccharide stimulated BAL cell production of TNF-alpha. Results: Eight subjects in the active group and 2 in the placebo group completed the study protocol. Eight weeks of oral NAC did not have a significant impact on TNF-alpha levels from BAL cells in-vivo in spite of a 59% increase in BAL GSH levels. Our in vitro studies showed a significant decline in TNF-alpha production from LPS stimulated BAL cells treated with 5 and 10 mM of NAC. Conclusions: Oral NAC increased GSH levels but failed to suppress in-vivo TNF-alpha production in contrast to effects in-vitro. Anti-oxidant therapy may still play a role in the management of sarcoidosis but therapy with better bioavailability or potency is needed to suppress the lung inflammatory response. (C) 2016 Elsevier Ltd. All rights reserved.

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