Literature DB >> 1516771

Hepatocarcinogenicity of chloral hydrate, 2-chloroacetaldehyde, and dichloroacetic acid in the male B6C3F1 mouse.

F B Daniel1, A B DeAngelo, J A Stober, G R Olson, N P Page.   

Abstract

The chlorinated acetaldehydes, chloral hydrate (CH) and 2-chloroacetaldehyde (CAA), have been identified as chlorination by-products in finished drinking water supplies. Although both chemicals are genotoxic, their potential for carcinogenicity had not been adequately explored. The studies reported here are chronic bioassays conducted with male B6C3F1 mice exposed to levels of 1 g/liter CH and 0.1 g/liter CAA via the drinking water for 104 weeks. Distilled water (H2O) served as the untreated control and dichloroacetic acid (DCA; 0.5 g/liter), another chlorine disinfection by-product, was included. The mean daily ingested doses were approximately 166 mg/kg/day for CH, 17 mg/kg/day for CAA, and 93 mg/kg/day for DCA. Evaluations included mortality, body weight, organ weights, gross pathology, and histopathology. The primary target organ was the liver as the organ weights and pathological changes in the other organs (spleen, kidneys, and testes) were comparable between the treated groups and the H2O control group. Liver weights were increased for all three test chemicals at the terminal euthanasia with the greatest increase seen in the CH and DCA groups. Hepatocellular necrosis was induced by all three test chemicals, and it was also most prevalent and severe in the CH and DCA groups. A significant increase in the prevalence of liver tumors was seen for all three chemicals. The strongest response was with DCA, in which 63% of the 104-week survivors had hepatocellular carcinomas (carcinomas) and 42% possessed hepatocellular adenomas (adenomas) and the combined prevalence for carcinomas plus adenoma was 75%. The corresponding prevalence rate for carcinomas, adenomas, and combined tumors were 46, 29, and 71%; 31, 8, and 38%; and 10, 5, and 15% for CH, CAA, and H2O, respectively. In addition to the tumors we evaluated the prevalence of a possible preneoplastic lesion, the hepatocellular hyperplastic nodule (nodules), a lesion which occurred in all three treated groups but not in the H2O group.

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Year:  1992        PMID: 1516771     DOI: 10.1016/0272-0590(92)90147-a

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  25 in total

1.  Dichloroacetate- and Trichloroacetate-Induced Modulation of Superoxide Dismutase, Catalase, and Glutathione Peroxidase Activities and Glutathione Level in the livers of Mice after Subacute and Subchronic exposure.

Authors:  Ezdihar A Hassoun; Jacquelyn Cearfoss
Journal:  Toxicol Environ Chem       Date:  2011-02       Impact factor: 1.437

2.  The induction of phagocytic activation by mixtures of the water chlorination by-products, dichloroacetate- and trichloroacetate, in mice after subchronic exposure.

Authors:  Ezdihar A Hassoun; Jacquelyn Cearfoss; Brian Musser; Sarah Krispinsky; Noor Al-Hassan; Ming-Cheh Liu
Journal:  J Biochem Mol Toxicol       Date:  2013-02-21       Impact factor: 3.642

3.  Chloral hydrate in pediatric magnetic resonance imaging: evaluation of a 10-year sedation experience administered by radiologists.

Authors:  Jorge Delgado; Rodrigo Toro; Simon Rascovsky; Andres Arango; Gabriel J Angel; Victor Calvo; Jorge A Delgado
Journal:  Pediatr Radiol       Date:  2014-08-21

4.  The induction of tumor necrosis factor-alpha, superoxide anion, myeloperoxidase, and superoxide dismutase in the peritoneal lavage cells of mice after prolonged exposure to dichloroacetate and trichloroacetate.

Authors:  Ezdihar A Hassoun; Jessica Spildener; Jacquelyn Cearfoss
Journal:  J Biochem Mol Toxicol       Date:  2010 Mar-Apr       Impact factor: 3.642

5.  2-Chloroacetaldehyde-induced cerebral glutathione depletion and neurotoxicity.

Authors:  C Sood; P J O'Brien
Journal:  Br J Cancer Suppl       Date:  1996-07

6.  F344/NTac Rats Chronically Exposed to Bromodichloroacetic Acid Develop Mammary Adenocarcinomas With Mixed Luminal/Basal Phenotype and Tgfβ Dysregulation.

Authors:  J B Harvey; H-H L Hong; S Bhusari; T-V Ton; Y Wang; J F Foley; S D Peddada; M Hooth; M DeVito; A Nyska; A R Pandiri; M J Hoenerhoff
Journal:  Vet Pathol       Date:  2015-03-02       Impact factor: 2.221

7.  Do Antioxidant Enzymes and Glutathione Play Roles in the Induction of Hepatic Oxidative Stress in Mice upon Subchronic Exposure to Mixtures of Dichloroacetate and Trichloroacetate?

Authors:  Ezdihar Hassoun; Jacquelyn Cearfoss
Journal:  Toxicol Environ Chem       Date:  2014-03       Impact factor: 1.437

8.  Dichloroacetate- and trichloroacetate-induced oxidative stress in the hepatic tissues of mice after long-term exposure.

Authors:  Ezdihar A Hassoun; Jacquelyn Cearfoss; Jessica Spildener
Journal:  J Appl Toxicol       Date:  2010-07       Impact factor: 3.446

9.  Evaluation of maternal and embryotoxic effects following the treatment of chloral hydrate in Drosophila melanogaster.

Authors:  Arif Ayar; Deniz Altun Çolak; Handan Uysal
Journal:  Cytotechnology       Date:  2014-08-07       Impact factor: 2.058

10.  Aqueous date fruit extract protects against lipid peroxidation and improves antioxidant status in the liver of rats subchronically exposed to trichloroacetic acid.

Authors:  Amira El Arem; Emna Behija Saafi; Fatma Ghrairi; Amira Thouri; Mouna Zekri; Amel Ayed; Abdelfattah Zakhama; Lotfi Achour
Journal:  J Physiol Biochem       Date:  2014-02-27       Impact factor: 4.158

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