Dybing E, Doe J, Groten J, Kleiner J, O'Brien J, Renwick A G, Schlatter J, Steinberg P, Tritscher A, Walker R, Younes M
National Institute of Public Health, Department of Environmental Medicine, PO Box 4404 Nydalen, N-0403, Oslo, Norway.
Food Chem Toxicol. 2002 Feb-Mar;40(2-3):237-82. doi: 10.1016/s0278-6915(01)00115-6.
Hazard characterisation of low molecular weight chemicals in food and diet generally use a no-observed-adverse-effect level (NOAEL) or a benchmark dose as the starting point. For hazards that are considered not to have thresholds for their mode of action, low-dose extrapolation and other modelling approaches may be applied. The default position is that rodents are good models for humans. However, some chemicals cause species-specific toxicity syndromes. Information on quantitative species differences is used to modify the default uncertainty factors applied to extrapolate from experimental animals to humans. A central theme for extrapolation is unravelling the mode of action for the critical effects observed. Food can be considered as an extremely complex and variable chemical mixture. Interactions among low molecular weight chemicals are expected to be rare given that the exposure levels generally are far below their NOAELs. Hazard characterisation of micronutrients must consider that adverse effects may arise from intakes that are too low (deficiency) as well as too high (toxicity). Interactions between different nutrients may complicate such hazard characterisations. The principle of substantial equivalence can be applied to guide the hazard identification and hazard characterisation of macronutrients and whole foods. Macronutrients and whole foods must be evaluated on a case-by-case basis and cannot follow a routine assessment protocol.
食品和饮食中低分子量化学物质的危害特征描述通常以未观察到有害作用水平(NOAEL)或基准剂量为起点。对于那些被认为其作用方式没有阈值的危害,可能会应用低剂量外推法和其他建模方法。默认的观点是啮齿动物是人类的良好模型。然而,一些化学物质会导致物种特异性的毒性综合征。关于定量物种差异的信息被用于修改从实验动物外推至人类时所应用的默认不确定性因素。外推的一个核心主题是阐明所观察到的关键效应的作用方式。食品可被视为一种极其复杂且多变的化学混合物。鉴于暴露水平通常远低于其未观察到有害作用水平,低分子量化学物质之间的相互作用预计很少见。微量营养素的危害特征描述必须考虑到摄入量过低(缺乏)以及过高(毒性)都可能产生不良影响。不同营养素之间的相互作用可能会使此类危害特征描述变得复杂。实质等同性原则可用于指导常量营养素和全食品的危害识别及危害特征描述。常量营养素和全食品必须逐案评估,不能遵循常规评估方案。