TIME COURSE OF OZONE-INDUCED NEUTROPHILIA IN NORMAL HUMANS

被引:121
作者
SCHELEGLE, ES
SIEFKIN, AD
MCDONALD, RJ
机构
[1] UNIV CALIF DAVIS,SCH MED,DEPT MED,DAVIS,CA 95616
[2] UNIV CALIF DAVIS,SCH MED,DEPT PEDIAT,DAVIS,CA 95616
来源
AMERICAN REVIEW OF RESPIRATORY DISEASE | 1991年 / 143卷 / 06期
关键词
D O I
10.1164/ajrccm/143.6.1353
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Five normal human subjects were exposed for 1 h to filtered air (FA) once and to 0.3 ppm O3 on 3 separate days. Bronchbalveolar lavage (BAL) fluid was obtained < 1 h after FA and either < 1, 6, or 24 h after O3 exposure. FEV1 was measured before the exposures and the BAL. The first aliquot [proximal airway (PA) sample] was analyzed separately from the pooled Aliquots 2 through 4 [distal airway and alveolar surface (DAAS) sample]. The data from the PA and DAAS samples were then combined to calculate the values that would have been obtained by pooling all BAL washes. FEV1 was significantly (p < 0.05) decreased 1 h after O3 exposure, but it returned to preexposure values at 6 and 24 h after O3. The percent of neutrophils in the PA sample was significantly elevated at < 1 h (3.7%) at 6 h (16.5%), and at 24 h (9.2%) after O3. The percent of neutrophils in the DAAS sample and calculated pooled values were significantly elevated at 6 h (4.1 and 7.6%) and at 24 h (5.1 and 5.8%) after O3. These data demonstrate that O3-induced symptoms, FEV1 decrements, and airway neutrophilia follow different time courses and indicate that the pooling of BAL washes may obscure the detection of an O3-induced bronchiolitis. The degree of neutrophilia in the BAL did not correlate with the sensitivity of the individual subjects when measured by acute changes in FEV1, suggesting a dichotomy of pathways that result in O3-induced airway neutrophilia and pulmonary function decrements.
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页码:1353 / 1358
页数:6
相关论文
共 22 条
[1]   DETECTION OF OZONE TOXICITY DURING CONTINUOUS EXERCISE VIA THE EFFECTIVE DOSE CONCEPT [J].
ADAMS, WC ;
SAVIN, WM ;
CHRISTO, AE .
JOURNAL OF APPLIED PHYSIOLOGY, 1981, 51 (02) :415-422
[2]  
BORG GUNNAR, 1961, K FYSIOGR SALLSKA PETS I LUND FORHANDL, V31, P105
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]  
CASTLEMAN WL, 1980, AM J PATHOL, V98, P811
[5]  
DAVIS GS, 1982, AM REV RESPIR DIS, V126, P611
[6]   EFFECTS OF O3 INHALATION DURING EXERCISE ON PULMONARY-FUNCTION AND BLOOD BIOCHEMISTRY [J].
DELUCIA, AJ ;
ADAMS, WC .
JOURNAL OF APPLIED PHYSIOLOGY, 1977, 43 (01) :75-81
[7]  
DUDDRIDGE M, 1988, THORAX, V43, P822
[8]  
Folinsbee L.J., 1978, ENV STRESS INDIVIDUA, P125
[9]  
GREEN JF, 1990, FASEB J, V4, pA1101
[10]   COMPARISON OF ACUTE OZONE-INDUCED NASAL AND PULMONARY INFLAMMATORY RESPONSES IN RATS [J].
HOTCHKISS, JA ;
HARKEMA, JR ;
SUN, JD ;
HENDERSON, RF .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1989, 98 (02) :289-302