REGIONAL INCREASES IN RAT NASAL EPITHELIAL-CELL PROLIFERATION FOLLOWING ACUTE AND SUBCHRONIC INHALATION OF FORMALDEHYDE

被引:116
作者
MONTICELLO, TM [1 ]
MILLER, FJ [1 ]
MORGAN, KT [1 ]
机构
[1] CHEM IND INST TOXICOL,POB 12137,6 DAVIS DR,RES TRIANGLE PK,NC 27709
关键词
D O I
10.1016/0041-008X(91)90246-B
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Short-term studies (9 days) in the rat have demonstrated that formaldehyde-induced nasal epithelial lesions are associated with increases in surface epithelial cell proliferation rates. The present studies were designed, in part, to investigate cell proliferation rates in the nasal epithelium of rats exposed to formaldehyde for a longer duration in order to determine if correlations exist between (1) the concentration-response in cell proliferation rate with the previously published formaldehyde bioassay tumor response; (2) sites of increased cell proliferation and the regions of the nasal passages that exhibit formaldehyde-induced cytotoxicity; and (3) sites of increased cell proliferation and the regions of the rat nasal passages previously determined to be most susceptible to neoplasia (i.e., the lateral meatus and nasal septum of the anterior nasal passages). Another important endpoint of this study was to provide data for a comparison of formaldehyde-induced responses in rats with previous findings in rhesus monkeys. Fischer-344 rats were exposed to 0, 0.7, 2, 6, 10, or 15 ppm formaldehyde for up to 6 weeks and pulse labeled with tritiated thymidine prior to each scheduled termination. Exposure to formaldehyde at 6 ppm or higher induced site-specific lesions in the nasal respiratory epithelium and was associated with increases in cell proliferation rate which remained statistically elevated throughout the 6 weeks. While a direct correlation between sites susceptible to formaldehyde-induced nasal cancer and increased cell proliferation was not evident, results from the present studies did demonstrate a clear correlation between sites of cellular injury and increases in cell proliferation and a concentration-dependent response which correlated with the previously published formaldehyde bioassay tumor response. Furthermore, this work demonstrated that form-aldehyde-induced responses in rats exposed to 6 ppm were morphologically similar to those reported in the rhesus monkey; however, the distribution of lesions between the two species differed significantly. © 1991.
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页码:409 / 421
页数:13
相关论文
共 42 条
[1]  
ALBERT RE, 1982, J NATL CANCER I, V68, P597
[2]   TOO MANY RODENT CARCINOGENS - MITOGENESIS INCREASES MUTAGENESIS [J].
AMES, BN ;
GOLD, LS .
SCIENCE, 1990, 249 (4972) :970-971
[3]  
BLAIR A, 1986, J NATL CANCER I, V76, P1071
[4]   UPTAKE OF INHALED GASES BY NOSE [J].
BRAIN, JD .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1970, 79 (03) :529-&
[5]   CONSIDERATION OF BOTH GENOTOXIC AND NONGENOTOXIC MECHANISMS IN PREDICTING CARCINOGENIC POTENTIAL [J].
BUTTERWORTH, BE .
MUTATION RESEARCH, 1990, 239 (02) :117-132
[6]   COVALENT BINDING OF INHALED FORMALDEHYDE TO DNA IN THE NASAL-MUCOSA OF FISCHER 344 RATS - ANALYSIS OF FORMALDEHYDE AND DNA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AND PROVISIONAL PHARMACOKINETIC INTERPRETATION [J].
CASANOVA, M ;
DEYO, DF ;
HECK, HD .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1989, 12 (03) :397-417
[7]   NASAL CAVITY DEPOSITION, HISTOPATHOLOGY, AND CELL-PROLIFERATION AFTER SINGLE OR REPEATED FORMALDEHYDE EXPOSURES IN B6C3F1 MICE AND F344 RATS [J].
CHANG, JCF ;
GROSS, EA ;
SWENBERG, JA ;
BARROW, CS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1983, 68 (02) :161-176
[8]   PHARMACOKINETICS, BIOCHEMICAL-MECHANISM AND MUTATION ACCUMULATION - A COMPREHENSIVE MODEL OF CHEMICAL CARCINOGENESIS [J].
CONOLLY, RB ;
REITZ, RH ;
CLEWELL, HJ ;
ANDERSEN, ME .
TOXICOLOGY LETTERS, 1988, 43 (1-3) :189-200
[9]  
CONOLLY RB, 1988, COMMENTS TOXICOL, V2, P305
[10]  
CRADDOCK VM, 1976, LIVER CELL CANCER, P153