Literature DB >> 12750748

NTP Carcinogenesis Bioassay of Melamine (CAS No. 108-78-1) in F344/N Rats and B6C3F1 Mice (Feed Study).

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Abstract

A NTP Carcinogenesis bioassay of melamine (>95% pure), a chemical intermediate in the manufacture of amino resins and plastics, was conducted by feeding diets containing 2,250 or 4,500 ppm melamine to groups of 50 male F344/N rats and 50 B6C3F1 mice of each sex for 103 weeks. Groups of 49 male rats, 50 female rats, 49 male mice, and 50 female mice served as controls. Mean body weights of dosed rats of each sex were lower than those of the controls after week 20. Survival of high-dose male rats was significantly lower (P</=0.05) than that of the controls. Survival of all other dosed rat groups was comparable with that of the respective controls. Transitional-cell carcinomas in the urinary bladder of male rats occurred with a statistically significant positive trend (P</=0.002; controls, 0/45; low-dose, 0/50; high-dose, 8/49, 16%) and the incidence in the high-dose group was significantly higher (P</=0.016) than that in the controls. A transitional-cell papilloma was observed in the urinary bladder of an additional high-dose male rat. These tumors were not observed in statistically significant proportions in female rats. Seven of the eight high-dose male rats with the transitional-cell carcinomas also had bladder stones. An association (P</=0.001) was found between bladder stones and bladder tumors in male rats. Chronic inflammation, distinguishable from the nephropathy observed in aging F344/N rats, was significantly increased (P</=0.01) in the kidney of dosed female rats (controls, 4/50,8%; low-dose, 17/50, 34%; high-dose, 41/50, 82%) and is attributed to the administration of melamine. The mean body weight of high-dose male mice was lower than that of controls after week 50 of the study. The mean body weights of dosed and control female mice were comparable throughout the study. Survival of high-dose male mice was significantly less (P<0.02) than that of the controls. Survival of all other dosed groups was similar to that of the respective controls. Acute and chronic inflammation and epithelial hyperplasia of the urinary bladder were found in increased incidence in dosed male mice. The incidence of bladder stones in dosed male mice was increased relative to controls (control, 2/45, 4%; low dose, 40/47, 85%; high-dose, 41/45, 93%); however, there was no evidence of bladder tumor development in this species. Also, four high-dose female mice had bladder stones without any tumors. Under the conditions of this bioassay, melamine was carcinogenic for male F344/N rats, causing transitional-cell carcinomas in the urinary bladder. With one exception, urinary bladder stones were observed in male rats that had transitional-cell carcinomas. Melamine was not carcinogenic for female F344/N rats or for B6C3F1 mice of either sex. Levels of Evidence of Carcinogenicity: Male Rats: Positive Female Rats: Negative Male Mice: Negative Female Mice: Negative Synonyms: 2,4,6-triamino-s-triazine; cyanurotriamide

Entities:  

Year:  1983        PMID: 12750748

Source DB:  PubMed          Journal:  Natl Toxicol Program Tech Rep Ser        ISSN: 0888-8051


  8 in total

1.  Dose-response assessment of nephrotoxicity from a 7-day combined exposure to melamine and cyanuric acid in F344 rats.

Authors:  Cristina C Jacob; Renate Reimschuessel; Linda S Von Tungeln; Greg R Olson; Alan R Warbritton; David G Hattan; Frederick A Beland; Gonçalo Gamboa da Costa
Journal:  Toxicol Sci       Date:  2010-10-28       Impact factor: 4.849

Review 2.  Melamine-related kidney stones and renal toxicity.

Authors:  Rishikesh P Dalal; David S Goldfarb
Journal:  Nat Rev Nephrol       Date:  2011-03-22       Impact factor: 28.314

3.  Dose-response assessment of nephrotoxicity from a twenty-eight-day combined-exposure to melamine and cyanuric acid in F344 rats.

Authors:  Gonçalo Gamboa da Costa; Cristina C Jacob; Linda S Von Tungeln; Nicholas R Hasbrouck; Greg R Olson; David G Hattan; Renate Reimschuessel; Frederick A Beland
Journal:  Toxicol Appl Pharmacol       Date:  2012-05-02       Impact factor: 4.219

Review 4.  Melamine toxicity.

Authors:  Carl G Skinner; Jerry D Thomas; John D Osterloh
Journal:  J Med Toxicol       Date:  2010-03

5.  Risks associated with melamine and related triazine contamination of food.

Authors:  Re Baynes; Je Riviere
Journal:  Emerg Health Threats J       Date:  2009-11-10

6.  Long-term follow-up of nephrotoxicity in rats administered both melamine and cyanuric acid.

Authors:  Takahiro Yasui; Takahiro Kobayashi; Atsushi Okada; Shuzo Hamamoto; Masahito Hirose; Kentaro Mizuno; Yasue Kubota; Yukihiro Umemoto; Noriyasu Kawai; Keiichi Tozawa; Bing Gao; Kenjiro Kohri
Journal:  BMC Res Notes       Date:  2014-02-08

7.  The melamine incident: implications for international food and feed safety.

Authors:  Céline Marie-Elise Gossner; Jørgen Schlundt; Peter Ben Embarek; Susan Hird; Danilo Lo-Fo-Wong; Jose Javier Ocampo Beltran; Keng Ngee Teoh; Angelika Tritscher
Journal:  Environ Health Perspect       Date:  2009-08-06       Impact factor: 9.031

8.  Evaluation of renal toxicity by combination exposure to melamine and cyanuric Acid in male sprague-dawley rats.

Authors:  Ji Yeon Son; Yoon Jong Kang; Kyeong Seok Kim; Tae Hyung Kim; Sung Kwang Lim; Hyun Jung Lim; Tae Cheon Jeong; Dal Woong Choi; Kyu Hyuck Chung; Byung Mu Lee; Hyung Sik Kim
Journal:  Toxicol Res       Date:  2014-06
  8 in total

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