McKinney J D, Fawkes J, Jordan S, Chae K, Oatley S, Coleman R E, Briner W
Environ Health Perspect. 1985 Sep;61:41-53. doi: 10.1289/ehp.856141.
TCDD and thyroxine have common molecular reactivity properties which enable them to present a planar face and lateral halogens in interactions with proteins. These molecular properties are consistent with the structure-toxicity relationship for TCDD and related compounds. Biological evidence is discussed including preliminary studies on the effects of TCDD exposure on tadpole growth and development which is consistent with the possible thyroxine-like activity of TCDD. The work suggests the possibility that toxicity is at least in part the expression of potent and persistent thyroid hormone activity (responses induced by TCDD which qualitatively correspond to those mediated by thyroid hormones). A mechanism for toxicity is proposed which involves receptor proteins; the planar aromatic system controls binding to cytosolic proteins and halogen substituents regulate binding to nuclear proteins. This simple model based on molecular reactivity sheds light on the diversified effects of TCDD and related compound toxicity and on certain thyroid hormone action. The model also permits predictions to be made with regard to the toxicity and thyroid hormone activity of untested compounds. In addition, the model suggests a general mechanism for hormone action based on metabolically regulated differential and cooperative protein receptor binding events in cellular compartments which can explain agonism, antagonism and potentiation within the framework of receptor occupancy theory.
2,3,7,8-四氯二苯并对二恶英(TCDD)和甲状腺素具有共同的分子反应特性,这使得它们在与蛋白质相互作用时能够呈现出一个平面表面和侧向卤素。这些分子特性与TCDD及相关化合物的结构-毒性关系一致。文中讨论了生物学证据,包括关于TCDD暴露对蝌蚪生长和发育影响的初步研究,这与TCDD可能具有的类甲状腺素活性相符。这项工作表明,毒性至少部分可能是强效且持久的甲状腺激素活性的表现(TCDD诱导的反应在性质上与甲状腺激素介导的反应相对应)。文中提出了一种涉及受体蛋白的毒性机制;平面芳香体系控制与胞质蛋白的结合,而卤素取代基调节与核蛋白的结合。这个基于分子反应性的简单模型揭示了TCDD及相关化合物毒性的多样化影响以及某些甲状腺激素的作用。该模型还允许对未测试化合物的毒性和甲状腺激素活性进行预测。此外,该模型提出了一种基于细胞区室中代谢调节的差异和协同蛋白受体结合事件的激素作用一般机制,这可以在受体占据理论的框架内解释激动作用、拮抗作用和增强作用。