Pulmonary glutathione levels in acute episodes of farmer's lung

Citation
J. Behr et al., Pulmonary glutathione levels in acute episodes of farmer's lung, AM J R CRIT, 161(6), 2000, pp. 1968-1971
Citations number
26
Categorie Soggetti
Cardiovascular & Respiratory Systems","da verificare
Journal title
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
ISSN journal
1073449X → ACNP
Volume
161
Issue
6
Year of publication
2000
Pages
1968 - 1971
Database
ISI
SICI code
1073-449X(200006)161:6<1968:PGLIAE>2.0.ZU;2-D
Abstract
Acute episodes of farmer's lung (FL) are associated with activation and mig ration of neutrophils into the lungs, causing oxidative stress. We conducte d a study to evaluate the effect of episodes of FL on antioxidant defense o f the lung by glutathione (GSH). A total of 15 patients with symptomatic FL (one female and 14 males, age 42 +/- 1 yr [mean +/- SEM]) underwent a stan dardized hay exposure test for 1 h and were then monitored through lung fun ction measurements for 6 h, after which bronchoalveolar lavage (BAL) was pe rformed. As a control, 10 asymptomatic farmers (AF) (two males and eight fe males, age 43 +/- 1 yr) underwent the same diagnostic procedures. At 3 to 6 h after antigen exposure, the lung function of FL patients was significant ly impaired (VC: -31 +/- 4%; single-breath diffusing capacity of carbon mon oxide [DLCO]: -17 +/- 3%; and PaO2: -14 +/- 2%, all versus baseline, wherea s in AF, only minor changes occurred VC: -4 +/- 5%; DLCO: -9 +/- 3%, and Pa O2: -5 +/- 2%, all versus baseline). The number of neutrophils in bronchoal veolar ravage fluid was increased in FL patients as compared with AF (29 +/ - 7 x 104/ml versus 10 +/- 7 x 10(4)/ml, p < 0.05). The concentrations of t otal and reduced glutathione (GSH, and GSH, respectively) in epithelial lin ing fluid were decreased in FL patients and increased in AF (GSHT: 292.5 +/ - 27.5 mu M versus 1,185.0 +/- 189.9 mu M, respectively, p < 0.001; GSH: 25 6.8 +/- 22.1 mu M versus 1,054.5 +/- 172.9 mu M, respectively, p < 0.001). These findings suggest that the individual ability to upregulate GSH in the alveolar space in response to an inflammatory stimulus may have implicatio ns for the development of symptomatic FL. We conclude that intrapulmonary G SH levels are distinctly different in patients with FL and AF, and that the regulation of GSH may play an important role in the pathogenesis of FL.