Dose-response studies on promoting and anticarcinogenic effects of phenobarbital and DDT in the rat hepatocarcinogenesis

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Abstract
Possible discrepancy between the dose level required for promoting action, when given after initiation process, and that needed to exert an anticarcinogenic effect when given simultaneously with a carcinogen, of hepatic promoters were investigated in an attempt to obtain a practical threshold dose of promoters. Phenobarbital (PB) and DDT were used as promoters and 3''-methyl-4-(dimethylamino)azobenzene (3''-Me-DAB) was used as the carcinogen. Male weanling rats were treated with 600 ppm 3''-Me-DAB for 3 wk followed by a diet containing a promoter at various dose levels (5-500 ppm), or the animals were treated with a low dose (100 ppm) of 3''-Me-DAB plus a promoter at various dose levels (20-500 ppm). The effects of promoters were measured by scoring size and number of enzyme-altered islands at weeks 12 and 24 of rat age. The promoting effect of PB and DDT was demonstrated in dose-dependent fashion, in the dose range of 10-500 ppm and 20-500 ppm, respectively. Promoters given simultaneously with a low dose of carcinogen enhanced the carcinogenesis at all the dose levels tested, quite in contrast with their inhibitory effect on carcinogenesis when given together with relatively high doses of carcinogens.

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