4.7 Article

Carcinogenicity of glycidamide in B6C3F1 mice and F344/N rats from a two-year drinking water exposure

期刊

FOOD AND CHEMICAL TOXICOLOGY
卷 86, 期 -, 页码 104-115

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2015.09.017

关键词

Acrylamide; Glycidamide; Tumorigenicity; Mice; Rats; Bioassay

资金

  1. Interagency Agreement between the National Institute of Environmental Health Sciences
  2. National Toxicology Program
  3. U.S. Food and Drug Administration, National Center for Toxicological Research (NCTR/FDA IAG) [224-12-0003]
  4. U.S. Food and Drug Administration, National Center for Toxicological Research (NIH/NTP IAG) [AES12013]
  5. Fundacao para a Ciencia e a Tecnologia, Portugal [RECI/QEQ-MED/0330/2012, UID/QUI/00100/2013]
  6. Fundação para a Ciência e a Tecnologia [RECI/QEQ-MED/0330/2012] Funding Source: FCT

向作者/读者索取更多资源

Acrylamide is a contaminant in baked and fried starchy foods, roasted coffee, and cigarette smoke. Previously we reported that acrylamide is a multi-organ carcinogen in B6C3F(1) mice and F344/N rats, and hypothesized that acrylamide is activated to an ultimate carcinogen through metabolism to the epoxide glycidamide. We have now examined the carcinogenic effects of glycidamide administered at 0, 0.0875, 0.175, 0.35 and 0.70 mM in drinking water to the same strains of rodents for two years. In male and female mice, there were significant increases in tumors of the Harderian gland, lung, forestomach, and skin. Female mice also had an increased incidence of tumors of the mammary gland and ovary. In male and female rats, there were significant increases in thyroid gland and oral cavity neoplasms and mononuclear cell leukemia. Male rats also had increases in tumors of the epididymis/testes and heart, while female rats demonstrated increases in tumors of the mammary gland, clitoral gland, and forestomach. A similar spectrum of tumors was obtained in mice and rats administered acrylamide. These data indicate that, under the conditions of these bioassays, acrylamide is efficiently metabolized to glycidamide and that the carcinogenic activity of acrylamide is due to its conversion into glycidamide. Published by Elsevier Ltd.

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