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Smith and Cabral (1980) exposed female Agus and Wistar rats to diets containing 100 mg/kg HCB for<br />

up to 90 or 75 weeks, respectively. An increased incidence of liver tumors (histological type not<br />

specified) due to HCB exposure was observed in both Agus and Wistar rats; tumor incidence was<br />

14/14 and 4/6, respectively, compared to 0/12 and 0/4, respectively, in the control animals.<br />

Male and female Syrian golden hamsters were exposed to diet containing 0, 200 or 400 mg/kg diet<br />

HCB for 90 days; 25-50 animals/group were sacrificed on the 91st day (Lambrecht et al., 1982). The<br />

remaining 25 animals/group were placed on control diet and sacrificed at 6 week intervals up to 1 year.<br />

Hepatoma incidence in the 200 and 400 mg/kg diet groups was 1/13 and 1/20, respectively, for males<br />

and 1/15 and 1/7, respectively for females. No hepatomas were noted in 43-50 control animals for<br />

each sex.<br />

Male and female Sprague-Dawley rats (94/sex/group) were fed diets containing 0, 75 or 150 mg/kg<br />

diet HCB for up to 2 years (Lambrecht et al., 1983a, b, 1986). Four animals/sex/group were killed at<br />

0, 1,2,3,4,8,16,32 and 64 weeks. Treatment-related increases in the incidence of hepatic tumors<br />

(hepatomas, hemangiomas, hepatocarcinomas and bile duct adenomas/carcinomas) and renal-cell<br />

adenomas were noted in both male and female animals. Tumor incidence data is noted in Table 3.<br />

Table 3.<br />

Hexachlorobenzene-induced hepatic tumors in male and female Sprague-Dawley rats<br />

(Lambrecht et al., 1983 a,b; 1986)<br />

Dose group<br />

(mg/kg diet)<br />

Tumor type<br />

Tumor incidence<br />

males females<br />

0 hepatoma/hemangioma 0/54 0/52<br />

75 10/52 23/56<br />

150 11/56 35/55<br />

0 hepatocarcinoma 0/54 0/52<br />

75 3/52 36/56<br />

150 4/56 48/55<br />

0 bile duct adenoma/carcinoma 0/54 1/52<br />

75 2/52 19/56<br />

150 2/56 29/55<br />

0 renal-cell adenomas 7/54 1/52<br />

75 41/52 7/56<br />

150 42/56 15/55<br />

Arnold et al. (1985) conducted two studies on the effects of chronic feeding of HCB in Sprague-<br />

Dawley rats. In the first study, male and female Sprague-Dawley rats were fed diets containing 0, 0.32,<br />

1.6, 8 or 40 mg/kg diet HCB for 3 months after weaning. Group sizes were 40/sex except for the<br />

control and high-dose groups (64 and 66/sex, respectively). After 3 months, the F 0 rats were bred and<br />

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