用于生态毒理学风险评估的化学品敏感性变异的来源和影响。

V E Forbes
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引用次数: 10

摘要

个人对有毒化学品反应的差异有几个原因,其中最重要的是遗传差异、环境影响(包括产妇影响和历史因素)和测量误差。有效的风险评估要求对毒物反应(例如LD50、EC50、LOEC、NOEC)的估计是精确的,即具有较窄的置信限,可重复的,即不同实验室必须获得相同或非常相似的结果,并且准确的,即它们必须提供毒物对实际生态系统影响的合理近似值。确定上述变异源中哪一个对毒物反应的影响最大,对生态毒理学试验的设计和解释都有影响。例如,如果遗传影响具有压倒一切的重要性,那么控制基因型(通过使用克隆或近交系)可以提高精度,但当目的是估计整个物种的毒性反应时,则以准确性为代价。同样,如果环境影响在控制对毒物的反应方面是最重要的,那么在标准温度、光线和食物制度下进行实验可能会提供高度可重复的测试结果,而这些结果与自然界中种群的反应几乎没有关系。虽然毫无疑问,控制变异的遗传和环境来源的标准生态毒理学测试准则(例如经合发组织)的发展已导致风险评估实践的改进,但进一步的进展将需要更复杂的方法来处理这些不确定性来源。有必要采用更系统的方法来量化毒性反应变异性的来源,并在关键风险评估终点正式结合与每个来源相关的误差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sources and implications of variability in sensitivity to chemicals for ecotoxicological risk assessment.

Variability among individuals in their responses to toxic chemicals arises from several sources, the most important of which are genetic differences, environmental influences (including maternal effects and historical factors) and measurement error. Effective risk assessment requires that estimates of toxicant response (e.g., LD50, EC50, LOEC, NOEC) are precise--that is, have narrow confidence limits-, repeatable--that is, different laboratories must obtain the same or very similar result-, and accurate--that is, they must provide a reasonable approximation of the effects of toxicants on real ecological systems. Determining which of the above-mentioned sources of variability has the greatest influence on toxicant response has implications for both the design and interpretation of ecotoxicological tests. If, for example, genetic influences are of overriding importance, controlling genotype (by using clones or inbred strains) can lead to greater precision but at the expense of accuracy when the objective is to estimate toxicant response for the species as a whole. Likewise, if environmental influences are of primary importance in controlling the response to toxicants, performing experiments under a standard temperature, light, and food regime may provide highly repeatable test results that have little relevance to the responses of populations in nature. Although there is little doubt that the development of standard ecotoxicological test guidelines (e.g., by the OECD), that control genetic and environmental sources of variability, has led to improvements in the practice of risk assessment, further advances will require a more sophisticated approach for dealing with these sources of uncertainty. There is a need for more systematic approaches for quantifying the sources of variability in toxicant response and for formally combining the error associated with each source in key risk assessment endpoints.

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