Yoneyama M, Ogata A, Hiraga K
Food Chem Toxicol. 1985 Aug;23(8):733-6. doi: 10.1016/0278-6915(85)90266-2.
The binding of [14C]thiabendazole ([14C]TBZ) to macromolecules in the liver, foetus and other tissues was investigated in Jcl:ICR mice on day 13 of gestation. TBZ suspended in olive oil was given orally in a dose of 1 g/kg body weight (5 microCi/mouse) and the mice (in groups of three) were killed 0.5, 1, 3, 6, 24 and 96 hr later. The bound radioactivity in the liver and foetus was at a maximum between 3 and 24 hr after treatment. The rate of decrease of the bound radioactivity was slower than that of total radioactivity. Bound radioactivity was also present in other tissues (including kidney, lung, heart, placenta and spleen). The level of bound radioactivity was measured in the liver and foetuses after oral administration of teratogenic doses of 200-1600 mg/kg. Disproportionate increases in bound radioactivity were observed in both tissues after administration of the highest dose.
在妊娠第13天的Jcl:ICR小鼠中,研究了[14C]噻苯达唑([14C]TBZ)与肝脏、胎儿及其他组织中大分子的结合情况。将悬浮于橄榄油中的TBZ以1 g/kg体重(5微居里/小鼠)的剂量口服给药,然后在给药后0.5、1、3、6、24和96小时处死小鼠(每组3只)。肝脏和胎儿中结合的放射性在治疗后3至24小时达到最大值。结合放射性的下降速率比总放射性的下降速率慢。其他组织(包括肾脏、肺、心脏、胎盘和脾脏)中也存在结合放射性。口服200 - 1600 mg/kg致畸剂量后,测定肝脏和胎儿中结合放射性的水平。给予最高剂量后,在这两种组织中均观察到结合放射性不成比例的增加。