SPECIES-DIFFERENCES IN IMPAIRMENT AND RECOVERY OF ALVEOLAR MACROPHAGE FUNCTIONS FOLLOWING SINGLE AND REPEATED OZONE EXPOSURES

被引:26
作者
OOSTING, RS
VANGOLDE, LMG
VERHOEF, J
VANBREE, L
机构
[1] NATL INST PUBL HLTH & ENVIRONM PROTECT,TOXICOL LAB,POB 1,3720 BA BILTHOVEN,NETHERLANDS
[2] STATE UNIV UTRECHT,VET BIOCHEM LAB,UTRECHT,NETHERLANDS
[3] STATE UNIV UTRECHT,EYKMAN WINKLER LAB MED MICROBIOL,UTRECHT,NETHERLANDS
关键词
D O I
10.1016/0041-008X(91)90299-T
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Effects of single (0.4 ppm for 3, 6, or 12 hr) and repeated (0.4 ppm, 12 hr/day for 3 or 7 days) in vivo ozone exposures on rat and mouse alveolar macrophage functions and cell number were investigated. Single ozone exposure of rats resulted in a small (∼15%) decrease in Fc-receptor-mediated phagocytosis and phorbol ester-induced superoxide production by the alveolar macrophages and was followed by recovery above control levels within 12 hr of exposure. Repeated exposures of rats for up to 7 days did not alter alveolar macrophage functions, with the exception of the effects of 3 days of exposure on superoxide production (71 ± 9% as compared with the controls). In mice, significant changes in alveolar macrophage functions were not observed until 12 hr of exposure (at that timepoint phagocytosis was 74 ± 2%). Repeated ozone exposures of mice did not cause a further decrease in phagocytosis (at Day 7, 74 ± 14%). Both after 3 and 7 days of repeated ozone exposure of mice, superoxide production by the alveolar macrophages was inhibited ∼50%. In rats and mice, repeated ozone exposures led to an increase in the number of alveolar macrophages. In mice, this increase appeared at a later time point (at Day 7 vs Day 3) and was less pronounced (at Day 7, 139 ± 9% vs 179 ± 17%) as compared with rats. In summary, our data show that rat and mouse alveolar macrophages have different susceptibilities to both single and repeated in vivo ozone exposures. © 1991.
引用
收藏
页码:170 / 178
页数:9
相关论文
共 30 条
[1]   DECREASED SUPEROXIDE ANION RADICAL PRODUCTION BY RAT ALVEOLAR MACROPHAGES FOLLOWING INHALATION OF OZONE OR NITROGEN-DIOXIDE [J].
AMORUSO, MA ;
WITZ, G ;
GOLDSTEIN, BD .
LIFE SCIENCES, 1981, 28 (20) :2215-2221
[2]   RAT LUNG RECOVERY FROM 3 DAYS OF CONTINUOUS EXPOSURE TO 0.75-PPM OZONE [J].
BASSETT, DJP ;
BOWENKELLY, E ;
ELBON, CL ;
REICHENBAUGH, SS .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1988, 25 (03) :329-347
[3]  
CANNING B J, 1990, American Review of Respiratory Disease, V141, pA250
[4]   ENHANCED PHAGOCYTOSIS BY ALVEOLAR MACROPHAGES INDUCED BY SHORT-TERM OZONE INSULT [J].
CHRISTMAN, CA ;
SCHWARTZ, LW .
ENVIRONMENTAL RESEARCH, 1982, 28 (02) :241-250
[5]   STUDY OF THE EFFECTS OF OZONE IN EMPHYSEMATOUS RATS [J].
DORMANS, JAMA ;
VANBREE, L ;
BOERE, AJF ;
MARRA, M ;
ROMBOUT, PJA .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1989, 26 (01) :1-18
[6]   ACUTE AND SUBCHRONIC OZONE INHALATION IN THE RABBIT - RESPONSE OF ALVEOLAR MACROPHAGES [J].
DRISCOLL, KE ;
VOLLMUTH, TA ;
SCHLESINGER, RB .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1987, 21 (1-2) :27-43
[7]  
DRISCOLL KE, 1988, INHAL TOXICOL, V1, P109
[9]  
GILMOUR M I, 1989, American Review of Respiratory Disease, V139, pA276
[10]   ADVERSE INFLUENCE OF OZONE ON PULMONARY BACTERICIDAL ACTIVITY OF MURINE LUNG [J].
GOLDSTEIN, E ;
TYLER, WS ;
HOEPRICH, PD ;
EAGLE, C .
NATURE, 1971, 229 (5282) :262-+