Poon R, Lecavalier P, Mueller R, Valli V E, Procter B G, Chu I
Environmental Health Directorate and Food Directorate, Health Protection Branch, Ottawa, Ontario, Canada.
Food Chem Toxicol. 1997 Feb;35(2):225-39. doi: 10.1016/s0278-6915(96)00064-6.
The subchronic oral toxicity of di(2-ethylhexyl) phthalate (DEHP) and di-n-octyl phthalate (DNOP) was studied. Groups of 10 male and 10 female Sprague-Dawley rats were administered DEHP in the diet at 0, 5, 50, 500 or 5000 ppm for 13 wk. In a separate study, groups of 10 male and 10 female Sprague-Dawley rats were given DNOP (5, 50, 500 and 5000 ppm) in the diet while control groups received basal diet containing 4% corn oil and positive control groups were fed a diet containing 5000 ppm DEHP. Growth rate and food consumption were not affected by treatment with either compound. Hepatomegaly was observed in the highest dose groups of both sexes administered DEHP but not in the DNOP-treated animals. At the highest dose, DNOP caused threefold (females) and 12-fold (males) increases in liver ethoxyresorufin-O-deethylase activity while DEHP did not. Mild changes in serum biochemistries were mostly confined to rats in the highest dose group of DEHP, and included increased serum albumin and albumin/globulin ratio in both sexes and decreased cholesterol in female rats. Mild vacuolations in the Sertoli cells were observed in male rats exposed to 500 ppm DEHP. At 5000 ppm DEHP, there was mild to moderate seminiferous tubule atrophy and Sertoli cell vacuolation in males, and rats of both sexes showed hepatic peroxisome proliferation. Both DEHP and DNOP at 5000 ppm caused mild histological changes in the thyroid consisting of reduced follicle size and colloid density, and the liver consisting of endothelial nuclear prominence, nuclear hyperchromicity and anisokaryosis. There was accentuation of zonation of the hepatic lobules and increased perivenous cytoplasmic vacuolation in DNOP-treated rats. Trace quantities (3-5 ppm) of DEHP and DNOP were detected in the liver, and 15-31 ppm were found in adipose tissue of the highest dose groups. The no observed-effect-level was judged to be 50 ppm in the diet or 3.7 mg/kg body weight/day for DEHP, and 500 ppm or 36.8 mg/kg body weight/day for DNOP.
研究了邻苯二甲酸二(2-乙基己基)酯(DEHP)和邻苯二甲酸二正辛酯(DNOP)的亚慢性经口毒性。将10只雄性和10只雌性斯普拉格-道利大鼠分为几组,在饲料中分别给予0、5、50、500或5000 ppm的DEHP,持续13周。在另一项研究中,将10只雄性和10只雌性斯普拉格-道利大鼠分为几组,在饲料中给予DNOP(5、50、500和5000 ppm),而对照组接受含4%玉米油的基础饲料,阳性对照组喂食含5000 ppm DEHP的饲料。两种化合物处理均未影响生长速率和食物消耗量。给予DEHP的两性最高剂量组均观察到肝肿大,但DNOP处理的动物未出现。在最高剂量下,DNOP使肝脏乙氧基异吩嗪酮-O-脱乙基酶活性增加了三倍(雌性)和十二倍(雄性),而DEHP则没有。血清生化指标的轻微变化主要局限于DEHP最高剂量组的大鼠,包括两性血清白蛋白和白蛋白/球蛋白比值升高,以及雌性大鼠胆固醇降低。暴露于500 ppm DEHP的雄性大鼠睾丸支持细胞出现轻度空泡化。在5000 ppm DEHP时,雄性大鼠出现轻度至中度曲细精管萎缩和支持细胞空泡化,两性大鼠均出现肝脏过氧化物酶体增殖。5000 ppm的DEHP和DNOP均引起甲状腺轻度组织学变化,表现为滤泡大小和胶体密度降低,肝脏表现为内皮细胞核突出、核深染和核大小不一。DNOP处理的大鼠肝小叶的带区化加重,静脉周围细胞质空泡化增加。在最高剂量组的肝脏中检测到痕量(3-5 ppm)的DEHP和DNOP,在脂肪组织中检测到15-31 ppm。DEHP的未观察到有害作用水平判定为饲料中50 ppm或体重3.7 mg/kg/天,DNOP为500 ppm或体重36.8 mg/kg/天。