Nelson B K
National Institute for Occupational Safety and Health, Division of Biomedical and Behavioral Science, Cincinnati, OH 45226.
Neurotoxicol Teratol. 1991 Nov-Dec;13(6):569-73. doi: 10.1016/0892-0362(91)90039-y.
Numerous factors must be considered in selecting exposure parameters for developmental neurotoxicity investigations. Whether employing a single dose during pregnancy, or continuous exposure from prepregnancy through early postnatal developmental periods, the following primary factors should be addressed: 1) Purpose of the study; 2) pharmacokinetics/pharmacodynamics; 3) biotransformation; 4) genotypic variables; 5) limiting factors, including the availability of test compounds for evaluation; and, 6) several general, miscellaneous factors. Whether a single, large dose of an exogenous agent is more toxic to the developing nervous system than a series of smaller doses depends upon the interaction of the physicochemical, pharmacokinetic, and pharmacodynamic properties of the agent with the genotypic features of the test organism.
在选择发育神经毒性研究的暴露参数时,必须考虑众多因素。无论是在孕期采用单剂量,还是从孕前到产后早期发育阶段进行持续暴露,都应考虑以下主要因素:1)研究目的;2)药代动力学/药效学;3)生物转化;4)基因型变量;5)限制因素,包括用于评估的受试化合物的可获得性;以及6)一些一般的、杂项因素。单一高剂量外源性物质对发育中的神经系统是否比一系列较小剂量更具毒性,取决于该物质的物理化学、药代动力学和药效学特性与受试生物体基因型特征之间的相互作用。