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Genome-Linked Toxic Responses to Dietary Iron OverloadCenter for Food Safety and Applied Nutrition, Food and Drug Administration, Washington, D.C. 20204, PVW{at}CFSAN.FDA.GOV
Center for Food Safety and Applied Nutrition, Food and Drug Administration, Washington, D.C. 20204
National Center for Toxicological Research, Jefferson, Arkansas 72079
National Center for Toxicological Research, Jefferson, Arkansas 72079
National Center for Toxicological Research, Jefferson, Arkansas 72079
National Center for Toxicological Research, Jefferson, Arkansas 72079
National Center for Toxicological Research, Food and Drug Administration, Jefferson, Arkansas 72079 Genome-related differences to Fe overload between and within rodent species were evaluated in the present study. Male B6C3F, mice, yellow and black C5YSF1 mice, and Fischer 344 (F344) rats were fed AIN-76A diets containing 35 (control), 1,500, 3,500, 5,000, or 10,000 µg carbonyl Fe/g for 12 wk. No effects on body weight gain were observed in the B6C3F, and black C5YSF, mice, whereas at all doses of Fe above the control, weight gain was reduced in yellow C5YSF1 mice and F344 rats. At the 10,000 µg Fe/g dose, 9 of 12 rats died, but there was no mortality among the mice. In all animals, there was a dose-related increase in liver nonheme Fe, and the Fe was stored in hepatocytes predominantly in the periportal region. There was significant hypertrophy of the hepatocytes in both B6C3F, mice and F344 rats fed the 10,000 µg Fe/g diet. PCNA assays showed significant stimulatory effects of the high dose of Fe on hepatocyte proliferation in the F344 rats and the C5YSF, mice but not in the B6C3F, mice. In the rat, there was pancreatic atrophy with loss of both endocrine and exocrine tissue. Morphometric evaluation of pancreas showed fewer β cells in B6C3F, and yellow C5YSF1 mice but not in the black C5YSF 1 mice. There were fewer islets in the yellow C5YSF1 mice, and total and mean islet areas were smaller than in the control mice. Rats in the 10,000 µg Fe/g dose group had markedly exacerbated dose-dependent nephropathy and changes in glomerular and tubular epithelium associated with Fe accumulation. The rats also showed degeneration of the germinal epithelium of the testis, formation of multinucleated giant cells, and lack of mature sperm.
Key Words: Iron toxicity • hepatocellular hemosiderosis • proliferating cell nuclear antigen • hepatocellular hypertrophy • pancreatic atrophy • β cells • nephropathy • testicular atrophy
Toxicologic Pathology, Vol. 25, No. 6,
556-564 (1997) This article has been cited by other articles:
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