Division of Science Integration, National Institute for Occupational Safety and Health, 1090 Tusculum Ave, MS C-15, Cincinnati, OH, USA.
Risk Anal. 2020 Dec;40(12):2561-2571. doi: 10.1111/risa.13547. Epub 2020 Jul 6.
Uncertainty in model predictions of exposure response at low exposures is a problem for risk assessment. A particular interest is the internal concentration of an agent in biological systems as a function of external exposure concentrations. Physiologically based pharmacokinetic (PBPK) models permit estimation of internal exposure concentrations in target tissues but most assume that model parameters are either fixed or instantaneously dose-dependent. Taking into account response times for biological regulatory mechanisms introduces new dynamic behaviors that have implications for low-dose exposure response in chronic exposure. A simple one-compartment simulation model is described in which internal concentrations summed over time exhibit significant nonlinearity and nonmonotonicity in relation to external concentrations due to delayed up- or downregulation of a metabolic pathway. These behaviors could be the mechanistic basis for homeostasis and for some apparent hormetic effects.
模型预测低暴露下的暴露反应的不确定性是风险评估中的一个问题。特别感兴趣的是生物系统中作为外部暴露浓度函数的一种物质的内部分布浓度。基于生理学的药代动力学 (PBPK) 模型允许估计靶组织中的内部暴露浓度,但大多数模型假设模型参数要么是固定的,要么是瞬间剂量依赖性的。考虑到生物调节机制的反应时间会引入新的动态行为,这些行为对慢性暴露下的低剂量暴露反应有影响。本文描述了一个简单的单室模拟模型,由于代谢途径的延迟上调或下调,内部浓度随时间的总和与外部浓度之间表现出显著的非线性和非单调关系。这些行为可能是体内平衡和某些明显的兴奋效应的机制基础。