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. 1986 Nov;69:109–117. doi: 10.1289/ehp.8669109

Chronic bioassays of chlorinated humic acids in B6C3F1 mice.

B L Van Duuren, S Melchionne, I Seidman, M A Pereira
PMCID: PMC1474334  PMID: 2949967

Abstract

Humic acids (Fluka), chlorinated to carbon:chlorine (C:Cl) ratios of 1:1 and 1:0.3, were administered to B6C3F1 mice, 50 males and 50 females per group, in the drinking water at a total organic carbon (TOC) level of 0.5 g/L. The mice were 6 to 8 weeks old at the beginning of the bioassays. The doses used were based on short-term (8 weeks) evaluations for toxicity, palatability, and weight gain. The chronic bioassays included the following control groups: unchlorinated humic acids (0.5 g/L), no-treatment (100 males and 100 females), dibromoethane (DBE, 2.0 mM in drinking water; positive control) and 0.44% sodium chloride in drinking water, i.e., at the same concentration as those receiving chlorinated humic acids. The chlorinated humic acids were prepared freshly and chemically assayed once per week. All chemicals were, with the exception of DBE, administered for 24 months; DBE was administered for 18 months. The volumes of solutions consumed were measured once weekly. All treatment groups showed normal weight gain except the DBE group. At the completion of exposure, the animals were sacrificed and necropsied, and tissue sections were taken for histopathology. No markedly significant increases in tumor incidences were evident in any of the organs and tissues examined in the chlorinated humic acid groups compared to unchlorinated humic acids and the no-treatment control groups. DBE caused the expected high incidence of squamous carcinomas of the forestomach. The chlorinated humic acids tested contained direct-acting alkylating agents, based on their reactivity with p-nitrobenzylpyridine (PNBP), and showed mutagenic activity in S. typhimurium.

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Selected References

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  1. Ames B. N., Mccann J., Yamasaki E. Methods for detecting carcinogens and mutagens with the Salmonella/mammalian-microsome mutagenicity test. Mutat Res. 1975 Dec;31(6):347–364. doi: 10.1016/0165-1161(75)90046-1. [DOI] [PubMed] [Google Scholar]
  2. Bull R. J., Robinson M., Meier J. R., Stober J. Use of biological assay systems to assess the relative carcinogenic hazards of disinfection by-products. Environ Health Perspect. 1982 Dec;46:215–227. doi: 10.1289/ehp.8246215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cameron T. P., Hickman R. L., Kornreich M. R., Tarone R. E. History, survival, and growth patterns of B6C3F1 mice and F344 rats in the National Cancer Institute Carcinogenesis Testing Program. Fundam Appl Toxicol. 1985 Jun;5(3):526–538. doi: 10.1016/0272-0590(85)90100-9. [DOI] [PubMed] [Google Scholar]
  4. Kool H. J., Kuper F., van Haeringen H., Koeman J. H. A carcinogenicity study with mutagenic organic concentrates of drinking-water in the Netherlands. Food Chem Toxicol. 1985 Jan;23(1):79–85. doi: 10.1016/0278-6915(85)90224-8. [DOI] [PubMed] [Google Scholar]
  5. Maltoni C., Lefemine G. Carcinogenicity bioassays of vinyl chloride: current results. Ann N Y Acad Sci. 1975 Jan 31;246:195–218. doi: 10.1111/j.1749-6632.1975.tb51094.x. [DOI] [PubMed] [Google Scholar]
  6. Meier J. R., Lingg R. D., Bull R. J. Formation of mutagens following chlorination of humic acid. A model for mutagen formation during drinking water treatment. Mutat Res. 1983 Jul;118(1-2):25–41. doi: 10.1016/0165-1218(83)90113-1. [DOI] [PubMed] [Google Scholar]
  7. Van Duuren B. L., Seidman I., Melchionne S., Kline S. A. Carcinogenicity bioassays of bromoacetaldehyde and bromoethanol--potential metabolites of dibromoethane. Teratog Carcinog Mutagen. 1985;5(6):393–403. doi: 10.1002/tcm.1770050603. [DOI] [PubMed] [Google Scholar]
  8. Viola P. L., Bigotti A., Caputo A. Oncogenic response of rat skin, lungs, and bones to vinyl chloride. Cancer Res. 1971 May;31(5):516–522. [PubMed] [Google Scholar]
  9. Ward J. M., Goodman D. G., Squire R. A., Chu K. C., Linhart M. S. Neoplastic and nonneoplastic lesions in aging (C57BL/6N x C3H/HeN)F1 (B6C3F1) mice. J Natl Cancer Inst. 1979 Sep;63(3):849–854. doi: 10.1093/jnci/63.3.849. [DOI] [PubMed] [Google Scholar]

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