Inhaled glucocorticosteroids decrease hydrogen peroxide level in expired air condensate in asthmatic patients

被引:55
作者
Antczak, A
Kurmanowska, Z
Kasielski, M
Nowak, D
机构
[1] Med Univ Lodz, Dept Pneumonol & Allergol, PL-90153 Lodz, Poland
[2] Med Univ Lodz, Dept Physiol, PL-90153 Lodz, Poland
关键词
bronchial asthma; airway inflammation; hydrogen peroxide; expired air; breath condensate; inhaled glucocorticosteroids;
D O I
10.1053/rmed.1999.0801
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
H2O2 is elevated in the exhaled air condensate in several inflammatory disorders of the lung, including bronchial asthma. and thus may reflect inflammatory processes in the airways. Exhaled H2O2 may be used to guide the antiinflammatory treatment of patients with asthma. Therefore in this study we analysed the effect of inhaled glucocorticosteroid beclomethasone for 4 weeks on H2O2 level in the exhaled air condensate. Seventeen asthmatics and 10 healthy subjects were included to the study. Eleven patients were given inhaled beclomethasone and six were given placebo (3M Health Care). In all patients pulmonary function rests were performed. H2O2 in the expired air condensate was measured spectrofluorimetically (homovanillic acid method). Inhaled beclomethasone significantly decreased H2O2 in the expired air condensate in the active-treatment group, with a fall from baseline on day 1 which remained on day 43 (follow-up) (P < 0.05), Exhaled H2O2 in the active-treatment group was significantly lower than that in placebo group (P < 0.05). A negative correlation between H2O2 and forced expiratory volume in 1 sec (FEVl) on day 29 was observed. The decrease in exhaled H2O2 in the active-treatment group was accompanied by an improvement in pulmonary function tests results. Inhaled glucocorticoids reduce the level of H2O2 in the expired air condensate of asthmatic patients over a 4-week period and this may reflect their anti-inflammatory activity in lung diseases.
引用
收藏
页码:416 / 421
页数:6
相关论文
共 37 条
[1]
Abraham W M, 1994, Adv Prostaglandin Thromboxane Leukot Res, V22, P131
[2]
[Anonymous], 1987, AM REV RESPIR DIS, V136, P1285
[3]
Increased hydrogen peroxide and thiobarbituric acid-reactive products in expired breath condensate of asthmatic patients [J].
Antczak, A ;
Nowak, D ;
Shariati, B ;
Krol, M ;
Piasecka, G ;
Kurmanowska, Z .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (06) :1235-1241
[4]
EFFICACY AND SAFETY OF INHALED CORTICOSTEROIDS IN ASTHMA - REPORT OF A WORKSHOP HELD IN EZE, FRANCE, OCTOBER 1992 [J].
BARNES, PJ ;
PEDERSEN, S .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 148 (04) :S1-S26
[5]
REACTIVE OXYGEN SPECIES AND AIRWAY INFLAMMATION [J].
BARNES, PJ .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 9 (03) :235-243
[6]
ANTIINFLAMMATORY ACTIONS OF STEROIDS - MOLECULAR MECHANISMS [J].
BARNES, PJ ;
ADCOCK, I .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1993, 14 (12) :436-441
[7]
BECASLEY R, 1989, AM REV RESPIR DIS, V139, P806
[8]
EOSINOPHILIC INFLAMMATION IN ASTHMA [J].
BOUSQUET, J ;
CHANEZ, P ;
LACOSTE, JY ;
BARNEON, G ;
GHAVANIAN, N ;
ENANDER, I ;
VENGE, P ;
AHLSTEDT, S ;
SIMONYLAFONTAINE, J ;
GODARD, P ;
MICHEL, FB .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 323 (15) :1033-1039
[9]
ENHANCED SUPEROXIDE PRODUCTION BY ALVEOLAR MACROPHAGES AND AIR-SPACE CELLS, AIRWAY INFLAMMATION, AND ALVEOLAR MACROPHAGE DENSITY CHANGES AFTER SEGMENTAL ANTIGEN BRONCHOPROVOCATION IN ALLERGIC SUBJECTS [J].
CALHOUN, WJ ;
REED, HE ;
MOEST, DR ;
STEVENS, CA .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 145 (02) :317-325
[10]
ENHANCED ALVEOLAR CELL LUMINOL-DEPENDENT CHEMILUMINESCENCE IN ASTHMA [J].
CLUZEL, M ;
DAMON, M ;
CHANEZ, P ;
BOUSQUET, J ;
DEPAULET, AC ;
MICHEL, FB ;
GODARD, P .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1987, 80 (02) :195-201