Assessment of the mutagenic potential of Cr(VI) in the oral mucosa of Big Blue® transgenic F344 rats

被引:24
作者
Thompson, Chad M. [1 ]
Young, Robert R. [2 ]
Suh, Mina [3 ]
Dinesdurage, Harshini R. [2 ]
Elbekai, Reem H. [2 ]
Harris, Mark A. [1 ]
Rohr, Annette C. [4 ]
Proctor, Deborah M. [3 ]
机构
[1] ToxStrategies Inc, Katy, TX 77494 USA
[2] BioReliance, Rockville, MD USA
[3] ToxStrategies Inc, Mission Viejo, CA USA
[4] Elect Power Res Inst, Palo Alto, CA USA
关键词
hexavalent chromium [Cr(VI); Big Blue((R)); transgenic rat; 4-nitroquinoline-1-oxide; mode of action; in vivo mutation; oral cavity; HEXAVALENT CHROMIUM; DRINKING-WATER; INTESTINAL EPITHELIA; INDUCED MUTATIONS; B6C3F1; MICE; CARCINOGENESIS; EXPOSURE; SALIVA; MODEL; CANCER;
D O I
10.1002/em.21952
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Exposure to high concentrations of hexavalent chromium [Cr(VI)] in drinking water was associated with an increased incidence of oral tumors in F344 rats in a 2-year cancer bioassay conducted by the National Toxicology Program. These tumors primarily occurred at 180 ppm Cr(VI) and appeared to originate from the gingival mucosa surrounding the upper molar teeth. To investigate whether these tumors could have resulted from a mutagenic mode of action (MOA), a transgenic mutation assay based on OECD Test Guideline 488 was conducted in Big Blue((R)) TgF344 rats. The mutagenic oral carcinogen 4-nitroquinoline-1-oxide (4-NQO) served as a positive control. Mutant frequency was measured in the inner gingiva with adjacent palate, and outer gingiva with adjacent buccal tissue. Exposure to 10 ppm 4-NQO in drinking water for 28 days increased mutant frequency in the cII transgene significantly, from 39.1 +/- 7.5 x 10(-6) to 688 +/- 250 x 10(-6) in the gingival/buccal region, and from 49.8 +/- 17.8 x 10(-6) to 1818 +/- 362 x 10(-6) in the gingival/palate region. Exposure to 180 ppm Cr(VI) in drinking water for 28 days did not significantly increase the mutant frequency in the gingival/buccal (44.4 +/- 25.4 x 10(-6)) or the gingival/palate (57.8 +/- 9.1 x 10(-6)) regions relative to controls. These data indicate that high (approximate to 180,000 times expected human exposure), tumorigenic concentrations of Cr(VI) did not significantly increase mutations in the gingival epithelium, and suggest that Cr(VI) does not act by a mutagenic MOA in the rat oral cavity. Environ. Mol. Mutagen. 56:621-628, 2015. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:621 / 628
页数:8
相关论文
共 60 条
[1]  
[Anonymous], 2013, OECD GUIDELINE TESTI
[2]  
[Anonymous], 2011, Guide for the Care and Use o f Laboratory Animals
[3]  
[Anonymous], TRANSG ROD SOM GERM
[4]   4-Nitroquinoline 1-oxide forms 8-hydroxydeoxyguanosine in human fibroblasts through reactive oxygen species [J].
Arima, Yaeno ;
Nishigori, Chikako ;
Takeuchi, Toru ;
Oka, Shigenori ;
Morimoto, Kanehisa ;
Utani, Atsushi ;
Miyachi, Yoshiki .
TOXICOLOGICAL SCIENCES, 2006, 91 (02) :382-392
[5]   DIFFERENTIAL TOXICITY AND CLEARANCE KINETICS OF CHROMIUM(III) OR CHROMIUM(VI) IN MICE [J].
BRYSON, WG ;
GOODALL, CM .
CARCINOGENESIS, 1983, 4 (12) :1535-1539
[6]   Analysis of repair and mutagenesis of chromium-induced DNA damage in yeast, mammalian cells, and transgenic mice [J].
Cheng, L ;
Liu, SJ ;
Dixon, K .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1998, 106 :1027-1032
[7]  
Cheng Lei, 2000, Journal of Environmental Pathology Toxicology and Oncology, V19, P239
[8]  
de Almeida Patricia Del Vigna, 2008, J Contemp Dent Pract, V9, P72
[9]   THE USE OF SHUTTLE VECTORS FOR MUTATION ANALYSIS IN TRANSGENIC MICE AND RATS [J].
DYCAICO, MJ ;
PROVOST, GS ;
KRETZ, PL ;
RANSOM, SL ;
MOORES, JC ;
SHORT, JM .
MUTATION RESEARCH, 1994, 307 (02) :461-478
[10]  
Enviromental Protection Agency, 2012, HUMAN HLTH SCOPING D