Poiger H, Schlatter C
Nature. 1979 Oct 25;281(5733):706-7. doi: 10.1038/281706a0.
Apart from its high toxicity, the chemical stability and persistence of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in the environment bring about additional hazards. However, until now there has been no evidence for degradation of this dioxin in biological systems, and it is considered unusual that a compound which is insusceptible to biological attack should be so extremely toxic. In in vitro studies with microsomal preparation from mouse, rat and rabbit liver, as well as in vivo, no metabolite of TCDD has been detected by several workers. Recent data, showing a lower toxicity of TCDD in rats after stimulation of the hepatic mixed-function oxidase, suggested possible metabolic transformation of this compound. In the present study, we used tritiated TCDD to search for metabolites in the bile of rats and found marked changes in lipophilicity and mobility in TLC of the excreted radioactivity. Treatment with diazomethane yielded at least two new compounds. These observations hinted at the formation of phenolic hydroxyl groups in the dioxin molecule.
除了具有高毒性外,2,3,7,8-四氯二苯并-对-二噁英(TCDD)在环境中的化学稳定性和持久性还带来了其他危害。然而,到目前为止,尚无证据表明这种二噁英在生物系统中会降解,而且一种不易受到生物攻击的化合物却具有极高的毒性,这被认为是不寻常的。在对小鼠、大鼠和兔肝脏微粒体制剂进行的体外研究以及体内研究中,多位研究人员均未检测到TCDD的代谢产物。最近的数据表明,在刺激肝脏混合功能氧化酶后,TCDD对大鼠的毒性降低,这表明该化合物可能发生了代谢转化。在本研究中,我们使用氚标记的TCDD在大鼠胆汁中寻找代谢产物,发现在薄层色谱(TLC)中排泄的放射性物质的亲脂性和迁移率发生了显著变化。用重氮甲烷处理产生了至少两种新化合物。这些观察结果暗示二噁英分子中形成了酚羟基。