Renwick A G
Clinical Pharmacology Group, University of Southampton, United Kingdom.
Regul Toxicol Pharmacol. 1999 Oct;30(2 Pt 2):S79-86. doi: 10.1006/rtph.1999.1330.
Noncancer effects are considered to show thresholds, such that no effect would be produced when the intake is below the threshold. Application of a 100-fold uncertainty factor to the no-observed-adverse-effect level (NOAEL) for the critical effect in animal studies provides an estimate of an intake for sensitive humans (the acceptable daily intake or ADI) without significant adverse health effects. The risks of intakes by humans above the ADI theoretically move the most sensitive subjects from negligible risk to possible risk. An increase in intake above the ADI would move the population distribution of internal dose toward the dose-response curve for sensitive subjects. The proportion of a population affected depends on the magnitude of the excess intake, the relationship of the NOAEL and the biological threshold in animals, and the coefficient of variation for the kinetic parameters (e.g., clearance and bioavailability) which determine the internal dose in humans. The severity of any effect in sensitive and high-intake individuals depends on the magnitude of the excess intake, the nature of the critical effect, and the slope of the dose-response relationship.
非致癌效应被认为存在阈值,即摄入量低于阈值时不会产生效应。在动物研究中,对关键效应的未观察到有害作用水平(NOAEL)应用100倍的不确定性系数,可得出敏感人群的摄入量估计值(每日可接受摄入量或ADI),且不会产生显著的健康不良影响。理论上,人类摄入量超过ADI会使最敏感的个体从可忽略风险转变为可能有风险。摄入量超过ADI会使体内剂量的人群分布向敏感个体的剂量反应曲线移动。受影响人群的比例取决于过量摄入量的大小、动物中NOAEL与生物学阈值的关系以及决定人体内部剂量的动力学参数(如清除率和生物利用度)的变异系数。敏感个体和高摄入量个体中任何效应的严重程度取决于过量摄入量的大小、关键效应的性质以及剂量反应关系的斜率。