INTERACTIONS OF XENOBIOTICS IN THE RESPIRATORY-TRACT FOLLOWING NONINHALATION ROUTES OF EXPOSURE

被引:1
作者
BRITTEBO, EB
BRANDT, I
机构
[1] Department of Pharmacology and Toxicology, Uppsala Biomedical Centre, Uppsala, S-75123, SLU
关键词
D O I
10.1093/ije/19.Supplement_1.S24
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Compounds of highly variable structure may induce toxic effects and tumours in the respiratory tract following peroral or parenteral administration in experimental animals. Such compounds are used in industrial processes or may be present in the food as contaminants or pesticide residues. This review gives examples of selective metabolism and toxicity of chemicals in different segments of the respiratory tract. Many of these compounds require metabolic activation to exert toxicity. Accordingly, the susceptibility of the respiratory tract to the effects of such agents may be influenced by other compounds modulating the activity of activating xenobiotic metabolizing enzymes. Dietary factors may alter the susceptibility to experimental lung carcinogenesis also via other mechanisms. As concluded from experimental data, the human lung may be exposed to a wide array of potentially toxic compounds present in the diet or the environment. Such exposures may constitute confounding factors in low-risk lung cancer epidemiology. © 1990 Oxford University Press.
引用
收藏
页码:S24 / S31
页数:8
相关论文
共 66 条
[1]   Pulmonary tumors in mice I The susceptibility of the lungs of albino mice to the carcinogenic action of 1, 2, 5 6-dibenzanthracene [J].
Andervont, HB .
PUBLIC HEALTH REPORTS, 1937, 52 :212-221
[2]   METABOLISM OF 2-ACETYLAMINOFLUORENE BY CLARA CELLS, TYPE-II CELLS AND ALVEOLAR MACROPHAGES ISOLATED FROM RABBIT LUNG, AND USE OF A NEW CHAMBER INCUBATION MUTAGENICITY TEST SYSTEM [J].
AUNE, T ;
DEVEREUX, TR ;
TVEITO, K .
CELL BIOLOGY AND TOXICOLOGY, 1985, 1 (03) :109-122
[3]   LUNG CARCINOGENESIS BY PROCARBAZINE CHLORATE IN BALB/C MICE [J].
BACCI, M ;
CAVALIERE, A ;
FRATINI, D .
CARCINOGENESIS, 1982, 3 (01) :71-73
[4]   METABOLISM OF 2,6-DICHLOROBENZONITRILE, 2,6-DICHLOROTHIOBENZAMIDE IN RODENTS AND GOATS [J].
BAKKE, JE ;
LARSEN, GL ;
STRUBLE, C ;
FEIL, VJ ;
BRANDT, I ;
BRITTEBO, EB .
XENOBIOTICA, 1988, 18 (09) :1063-1075
[5]   SITES FOR XENOBIOTIC ACTIVATION AND DETOXICATION WITHIN THE RESPIRATORY-TRACT - IMPLICATIONS FOR CHEMICALLY-INDUCED TOXICITY [J].
BARON, J ;
BURKE, JP ;
GUENGERICH, FP ;
JAKOBY, WB ;
VOIGT, JM .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1988, 93 (03) :493-505
[6]   EVIDENCE FOR CLARA CELL AS A SITE OF CYTOCHROME P450-DEPENDENT MIXED-FUNCTION OXIDASE ACTIVITY IN LUNG [J].
BOYD, MR .
NATURE, 1977, 269 (5630) :713-715
[7]  
BOYD MR, 1980, CRC CRIT R TOXICOL, P105
[8]   PCB METHYL SULFONES AND RELATED-COMPOUNDS - IDENTIFICATION OF TARGET-CELLS AND TISSUES IN DIFFERENT SPECIES [J].
BRANDT, I ;
BERGMAN, A .
CHEMOSPHERE, 1987, 16 (8-9) :1671-1676
[9]   IRREVERSIBLE BINDING AND TOXICITY OF THE HERBICIDE DICHLOBENIL (2,6-DICHLOROBENZONITRILE) IN THE OLFACTORY MUCOSA OF MICE [J].
BRANDT, I ;
BRITTEBO, EB ;
FEIL, VJ ;
BAKKE, JE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 103 (03) :491-501
[10]   DISTRIBUTION OF THE CARCINOGENIC TRYPTOPHAN PYROLYSIS PRODUCT TRP-P-1 IN CONTROL, 9-HYDROXYELLIPTICINE AND BETA-NAPHTHOFLAVONE PRETREATED MICE [J].
BRANDT, I ;
GUSTAFSSON, JA ;
RAFTER, J .
CARCINOGENESIS, 1983, 4 (10) :1291-1296