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Published ahead of print on January 15, 2004, doi:10.1164/rccm.200308-1104OC
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American Journal of Respiratory and Critical Care Medicine Vol 169. pp. 822-828, (2004)
© 2004 American Thoracic Society


Original Article

Improvement of Alveolar Glutathione and Lung Function but Not Oxidative State in Cystic Fibrosis

Matthias Griese, Jan Ramakers, Angela Krasselt, Vitaliy Starosta, Silke van Koningsbruggen, Rainald Fischer, Felix Ratjen, Bernhard Müllinger, Rudolf M. Huber, Konrad Maier, Ernst Rietschel and Gerhard Scheuch

Department of Pediatrics, Ludwig Maximilians University, Munich; Department of Nutrition, University of Hohenheim, Hohenheim; Department of Pediatrics, University of Cologne, Cologne; Inamed, Gauting; Department of Internal Medicine, Ludwig Maximilians University, Munich; Department of Pediatrics, University of Essen, Essen; and Institute for Inhalation Biology, GSF-Research Center for Environment and Health, Neuherberg, Germany

Correspondence and requests for reprints should be addressed to Matthias Griese, M.D., Dr. von Haunersches Kinderspital, Ludwig-Maximilians-University, Lindwurmstrasse 4, D-80337 Munich, Germany. E-mail: matthias.griese{at}med.uni-muenchen.de

Chronic neutrophilic inflammation leads to oxidative damage, which may play an important role in the pathogenesis of cystic fibrosis lung disease. Bronchoalveolar lavage levels of the antioxidant glutathione are diminished in patients with cystic fibrosis. Here we evaluated the effects of glutathione aerosol on lower airway glutathione levels, lung function, and oxidative status. Pulmonary deposition of a radiolabeled monodisperse aerosol generated with a Pari LC Star nebulizer (Allergy Asthma Technology, Morton Grove, IL) connected to an AKITA inhalation device (Inamed, Gauting, Germany) was determined in six patients. In 17 additional patients bronchoalveolar lavage fluid was assessed before and after 14 days of inhalation with thrice-daily doses of 300 or 450 mg of glutathione. Intrathoracic deposition was 86.3 ± 1.4% of the emitted dose. Glutathione concentration in lavage 1 hour postinhalation was increased three- to fourfold and was still almost doubled 12 hours postinhalation. FEV1 transiently dropped after inhalation but increased compared with pretreatment values after 14 days (p < 0.001). This improvement was not related to the lavage content of oxidized proteins and lipids, which did not change with treatment. These results show that, using a new inhalation device with high efficacy, glutathione treatment of the lower airways is feasible. Reversion of markers of oxidative injury may need longer treatment, higher doses, or different types of antioxidants.

Key Words: aerosol • antioxidant • bronchoalveolar lavage fluid • deposition • neutrophils




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