Co-carcinogenic Effect of Retinyl Acetate on Forestomach Carcinogenesis of Male F344 Rats Induced with Butylated Hydroxyanisole

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Induction of cell proliferation in the forestomach of F344 rats following subchronic administration of styrene 7,8-oxide and butylated hydroxyanisole.

The question addressed was whether stimulation of cell proliferation could be responsible for tumor induction in the forestomach by styrene 7,8-oxide (SO). Male F344 rats were treated for 4 weeks with 0, 137, 275, and 550 mg/kg SO by p.o. gavage 3 times/week. Positive controls received 0, 0.5, 1, and 2% butylated hydroxyanisole (BHA) in the diet for 4 weeks. Twenty-four h before termination of ...

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Induction of Cell Proliferation in the Forestomach of F344 Rats FoUowing Subchronic Administration of Styrene 7,8-0xide and Butylated Hydroxyanisole

for the 2% diet). to protein in vivo (20, 21). lt is possible, therefore, that SO and BHA were carcinogenic in the forestomach via a similar "nongenotoxic" mechanism of action, i.e., the stimulation 01' cell division induced by cytotoxicity and regenerative hyperplasia. This mechanism has been postulated for various forestomach carcinogens (22). BHA was demonstrated to have a strong hyperplasio...

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Induction of Cell Proliferation in the Forestomach of F344 Rats Following Subchronic Administration of Styrà ̈ne7,8-Oxide and Butylated Hydroxyanisole

The question addressed was whether stimulation of cell proliferation could be responsible for tumor induction in the forestomach by styrà ̈ne 7,8-oxide (SO). Male F344 rats were treated for 4 weeks with 0, 137, 275, and 550 mg/kg SO by p.o. gavage 3 times/week. Positive controls received 0, 0.5, 1, and 2% butylated hydroxyanisole (BHA) in the diet for 4 weeks. Twenty-four h before termination of...

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Different Modifying Response of Butylated Hydroxyanisole, Butylated Hydroxytoluene, and Other Antioxidants in A'jjV-Dibutylnitrosamine Esophagus and Forestomach Carcinogenesis of Rats1

The modifying effects of antioxidants were examined in a carcinogenesis system after \, V-ililnilvlniinisamiiic treatment. Male F344 rats were given 0.05% V, Vdilnilylnhrosarnmiin their drinking water for 4 wk and then treated with basal diet containing 2% butylated hydroxyanisole (BHA), 1% butylated hydroxytoluene (BHT) with 7 ppm vitamin K, 0.8% ethoxyquin, 5% sodium L-ascorbate, 57. sodium e...

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ژورنال

عنوان ژورنال: Japanese Journal of Cancer Research

سال: 1988

ISSN: 0910-5050

DOI: 10.1111/j.1349-7006.1988.tb01594.x