LACK OF RENAL TUMOR-INITIATING ACTIVITY OF A SINGLE DOSE OF POTASSIUM BROMATE, A GENOTOXIC RENAL CARCINOGEN IN MALE F344/NCR RATS

被引:22
作者
KURATA, Y
DIWAN, BA
WARD, JM
机构
[1] NCI,DIV CANC ETIOL,COMP CARCINOGENESIS LAB,TUMOUR PATHOL & PATHOGENESIS SECT,FREDERICK,MD 21702
[2] PRI DYNCORP,BIOL CARCINOGENESIS & DEV PROGRAM,FREDERICK,MD 21702
[3] NCI,FREDERICK CANC RES & DEV CTR,FREDERICK,MD 21702
关键词
D O I
10.1016/0278-6915(92)90041-I
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The renal tumour-initiating activity of potassium bromate (KBrO3), a known genotoxic rat renal carcinogen, was investigated in male F344/NCr rats. 6-wk-old rats were given KBrO3 intragastrically as a single dose of 300 mg/kg body weight, which was confirmed by our preliminary toxicity study as a maximum tolerated single dose for this strain of rat. Starting 2 wk after KBrO3 treatment, groups of 39 rats received either a basal diet or a diet containing 4000 ppm barbital sodium (BBNa) as a promoting regimen and were killed at 30, 52, or 104 wk. Control rats received either dietary BBNa (4000 ppm) or the basal diet alone from wk 2 to 52 or 104 wk. Nephropathy was observed in all rats treated with KBrO3 followed by BBNa at 30 wk and in rats receiving BBNa alone, but not in rats exposed to KBrO3 alone. Dysplastic renal tubular cell foci (DTF), putative preneoplastic renal tubular cell lesions were found associated with nephropathy in rats exposed to KBrO3 followed by BBNa from 47 wk. The incidences and multiplicities of DTF and renal tubular cell tumours observed from 31 to 104 wk revealed no initiating effect of KBrO3 treatment. These results indicate that the KBrO3 dose of 300 mg/kg did not initiate renal carcinogenesis.
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页码:251 / 259
页数:9
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