Lecavalier P, Chu I, Yagminas A, Villeneuve D C, Poon R, Feeley M, Håkansson H, Ahlborg U G, Valli V E, Bergman A, Seegal R F, Kennedy S W
Health Protection Branch, Health Canada, Ottawa, Ontario, Canada.
J Toxicol Environ Health. 1997 Jun 27;51(3):265-77. doi: 10.1080/00984109708984026.
The subchronic toxicity of 2,2',3,3',4,4'-hexachlorobiphenyl (PCB 128) was investigated in rats following dietary exposure at 0, 0.05, 0.5, 5, or 50 ppm for 13 wk. The growth rate was not affected by treatment and no apparent clinical signs of toxicity were observed. There was a significant increase in liver weight in the 50 ppm females. The liver ethoxyresorufin deethylase (EROD) activity was increased by five- and fourfold in the highest dose males and females, respectively, while aminopyrine demethylase (ADPM) activity was significantly increased only in the highest dose females. Liver vitamin A was significantly reduced in the highest dose females. No other biochemical or hematological effects were observed. Treatment-related histopathological changes were seen in the thyroid and liver, and to a lesser extent in the bone marrow and thymus. Residue data showed a dose-dependent accumulation of PCB 128 in the following tissues: fat, liver, kidney, brain, spleen, and serum, with the highest concentration being found in fat followed by liver and kidney. Based on these data, the no-observable-adverse-effect level of PCB 128 was judged to be 0.5 ppm in diet or 42 micrograms/kg body weight.
研究了大鼠经口摄入0、0.05、0.5、5或50 ppm的2,2',3,3',4,4'-六氯联苯(PCB 128)13周后的亚慢性毒性。生长速率不受处理影响,未观察到明显的毒性临床体征。50 ppm组的雌性大鼠肝脏重量显著增加。最高剂量组的雄性和雌性大鼠肝脏乙氧基异吩唑酮脱乙基酶(EROD)活性分别增加了五倍和四倍,而氨基比林脱甲基酶(ADPM)活性仅在最高剂量组的雌性大鼠中显著增加。最高剂量组的雌性大鼠肝脏维生素A显著降低。未观察到其他生化或血液学影响。在甲状腺和肝脏中观察到与处理相关的组织病理学变化,在骨髓和胸腺中观察到的变化程度较小。残留数据显示,PCB 128在以下组织中呈剂量依赖性蓄积:脂肪、肝脏、肾脏、脑、脾和血清,其中脂肪中的浓度最高,其次是肝脏和肾脏。基于这些数据,PCB 128的无可见有害作用水平被判定为饮食中0.5 ppm或体重42微克/千克。