Short-term inhalation exposure of healthy and compromised rats and mice to fine and ultrafine carbon particles

被引:8
作者
Arts, JHE
Spoor, SM
Muijser, H
机构
[1] TNO, Nutr & Food Res Inst, Dept Target Organ Toxicol, NL-3700 AJ Zeist, Netherlands
[2] Univ Calif Irvine, Irvine, CA USA
[3] RIVM, Natl Inst Publ Hlth & Environm, Hlth Effects Res Lab, Bilthoven, Netherlands
关键词
D O I
10.1080/08958378.2000.11463221
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Epidemiological studies have consistently shown associations between acute pulmonary effects and relatively low levels of ambient particulate matter (PM). The present study was carried out to examine the pulmonary toxicity of inhaled fine (FCB) and ultrafine carbon (UFC) particles as model compounds for carbonaceous (primary) PM, and to identify whether particle sizer particle number, and/or mass could be critical in inducing the deleterious effects. Healthy and compromised rats and mice were exposed for 4 h/day during 3 consecutive days to 10(4) or 10(5) fine carbon black (similar to 300-500 nm), or 10(5) or 10(6) ultrafine carbon (similar to 30-60 nm) particles/cm(3), covering a mass range of about 10 to 10,000 mu g/m(3). Separate groups of rats were also exposed to a combination of FCB and fine ammonium nitrate at similar number and mass concentrations. Animals were sacrificed the day after the last exposure to determine their pulmonary responses using bronchoalveolar lavage fluid (BALF) analysis and lung histopathology. Exposure to FCB resulted in early signs of lung injury. Effects were not enhanced in compromised animals when compared to healthy animals. Exposure to UFC particles at similar and higher number concentrations did not induce any biologically relevant changes. These data may indicate that at number concentrations occurring in ambient air, the size of the particles (in air) is more important than their number.
引用
收藏
页码:261 / 266
页数:6
相关论文
共 14 条
[1]   A MULTIPLE-PATH MODEL OF PARTICLE DEPOSITION IN THE RAT LUNG [J].
ANJILVEL, S ;
ASGHARIAN, B .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1995, 28 (01) :41-50
[2]  
Cassee F. R., 1999, 650010018 RIVM
[3]   Comparison of the uptake of fine and ultrafine TiO2 in a tracheal explant system [J].
Churg, A ;
Stevens, B ;
Wright, JL .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1998, 274 (01) :L81-L86
[4]   Ultrafine (nanometre) particle mediated lung injury [J].
Donaldson, K ;
Li, XY ;
MacNee, W .
JOURNAL OF AEROSOL SCIENCE, 1998, 29 (5-6) :553-560
[5]   INCREASED PULMONARY TOXICITY OF ULTRAFINE PARTICLES .1. PARTICLE CLEARANCE, TRANSLOCATION, MORPHOLOGY [J].
FERIN, J ;
OBERDORSTER, G ;
PENNEY, DP ;
SODERHOLM, SC ;
GELEIN, R ;
PIPER, HC .
JOURNAL OF AEROSOL SCIENCE, 1990, 21 (03) :381-384
[6]   PULMONARY RETENTION OF ULTRAFINE AND FINE PARTICLES IN RATS [J].
FERIN, J ;
OBERDORSTER, G ;
PENNEY, DP .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 6 (05) :535-542
[7]   INCREASED EXPRESSION OF MANGANESE-CONTAINING SUPEROXIDE-DISMUTASE IN RAT LUNGS AFTER INHALATION OF INFLAMMATORY AND FIBROGENIC MINERALS [J].
JANSSEN, YMW ;
MARSH, JP ;
DRISCOLL, KE ;
BORM, PJA ;
OBERDORSTER, G ;
MOSSMAN, BT .
FREE RADICAL BIOLOGY AND MEDICINE, 1994, 16 (03) :315-322
[8]   Free radical activity and pro-inflammatory effects of particulate air pollution (PM(10)) in vivo and in vitro [J].
Li, XY ;
Gilmour, PS ;
Donaldson, K ;
MacNee, W .
THORAX, 1996, 51 (12) :1216-1222
[9]  
MACNEE W, 1997, ANN OCCUP HYG S1, V41, P7
[10]   CORRELATION BETWEEN PARTICLE-SIZE, IN-VIVO PARTICLE PERSISTENCE, AND LUNG INJURY [J].
OBERDORSTER, G ;
FERIN, J ;
LEHNERT, BE .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1994, 102 :173-179