Hassoun E A
University of Baghdad, Department of Toxicology, College of Pharmacy, Iraq.
Arch Toxicol. 1987 Dec;61(2):145-9. doi: 10.1007/BF00661373.
Interactions of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), and other ligands of the Ah-receptor, had been studied in vivo, in pregnant NMRI mice, and in vitro, in the fetal thymus organ culture system. Benzo(a)pyrene (BP) increased TCDD-induced fetolethality, whereas it did not affect the rate of cleft palate formation. This may indicate that the mechanism of TCDD-induced fetal death is different from that of TCDD-induced cleft palate. 2,3,7,8-Tetrachlorodibenzofuran (TCDBF) and 3,3',4,4'-tetrachloroazoxybenzene (TCAOB) were added together to the thymus organ culture, each at a concentration that caused about 25-50% lymphoid development inhibition. Such treatment resulted in an additive effect of about 75%. Similarly, when the slightly toxic beta-naphthoflavone (BN) was added together with TCDD to the same culture system, it caused a significant increase in the lymphoid inhibitory effect of the latter compound. These may all suggest a common mechanism of action for TCDD and other ligands, which may involve a direct interaction with the receptors present in the thymus.
在怀孕的NMRI小鼠体内以及在胎儿胸腺器官培养系统中对2,3,7,8-四氯二苯并-对-二噁英(TCDD)及芳烃受体的其他配体之间的相互作用进行了研究。苯并(a)芘(BP)增加了TCDD诱导的胚胎致死率,而它并不影响腭裂形成的发生率。这可能表明TCDD诱导胎儿死亡的机制与TCDD诱导腭裂的机制不同。将2,3,7,8-四氯二苯并呋喃(TCDBF)和3,3',4,4'-四氯偶氮苯(TCAOB)以各自导致约25%-50%淋巴细胞发育抑制的浓度一起添加到胸腺器官培养物中。这样的处理导致了约75%的相加效应。同样,当将低毒的β-萘黄酮(BN)与TCDD一起添加到同一培养系统中时,它使后一种化合物的淋巴细胞抑制作用显著增强。这些可能都表明TCDD和其他配体存在共同的作用机制,这可能涉及与胸腺中存在的受体直接相互作用。