Dobrev I D, Andersen M E, Yang R S
Center for Environmental Toxicology and Technology, Department of Environmental Health, Colorado State University, Fort Collins 80523, USA.
Arch Toxicol. 2001 May;75(3):134-44. doi: 10.1007/s002040100216.
The volatile organic solvents trichloroethylene (TCE), tetrachloroethylene (perchloroethylene, PERC), and 1,1,1-trichloroethane (methylchloroform, MC) are widely distributed environmental pollutants and common contaminants of many chemical waste sites. To investigate the mode of pharmacokinetic interactions among TCE, PERC, and MC and to calculate defined "interaction thresholds", gas-uptake experiments were performed using a closed-chamber exposure system. In each experiment, two rats (Fischer 344, male, 8-9 weeks old) were exposed to different initial concentrations of TCE, PERC, and MC, applied singly or as a mixture, and their concentration in the gas phase of the chamber was monitored over a period of 6 h. A physiologically based pharmacokinetic (PBPK) model was developed to test multiple mechanisms of inhibitory interactions, i.e., competitive, non-competitive, or uncompetitive. All mixture exposure data were accurately described by a system of equations in which a PBPK model was provided for each chemical and each was regarded as an inhibitor of the others' metabolism. Sensitivity-analysis techniques were used to investigate the impact of key parameters on model output and optimize experimental design. Model simulations indicated that, among these three chemicals, the inhibition was competitive. The PBPK model was extended to assess occupationally relevant exposures at or below the current threshold-limit values (TLVs). Based on 10% elevation in TCE blood levels as a criterion for significant interaction and assuming TCE exposure is set at TLV of 50 ppm, the calculated interaction thresholds for PERC and MC were 25 and 135 ppm, respectively. TLV exposures to binary TCE/PERC mixture were below the 10% significance level. The interaction threshold for TCE and MC co-exposure would be reached at 50 and 175 ppm, respectively. Such interactive PBPK models should be of value in risk assessment of occupational and environmental exposure to solvent mixtures.
挥发性有机溶剂三氯乙烯(TCE)、四氯乙烯(全氯乙烯,PERC)和1,1,1 - 三氯乙烷(甲基氯仿,MC)是广泛分布的环境污染物,也是许多化学废物场地的常见污染物。为了研究TCE、PERC和MC之间的药代动力学相互作用模式,并计算特定的“相互作用阈值”,使用密闭腔室暴露系统进行了气体摄取实验。在每个实验中,将两只大鼠(Fischer 344,雄性,8 - 9周龄)暴露于不同初始浓度的TCE、PERC和MC,单独或混合使用,并在6小时内监测腔室气相中它们的浓度。建立了基于生理的药代动力学(PBPK)模型来测试抑制相互作用的多种机制,即竞争性、非竞争性或反竞争性。所有混合物暴露数据都通过一个方程组准确描述,其中为每种化学物质提供了一个PBPK模型,并且每种物质都被视为其他物质代谢的抑制剂。使用敏感性分析技术来研究关键参数对模型输出的影响并优化实验设计。模型模拟表明,在这三种化学物质中,抑制作用是竞争性的。PBPK模型被扩展以评估当前阈限值(TLV)及以下与职业相关的暴露。以TCE血药浓度升高10%作为显著相互作用的标准,并假设TCE暴露设定为50 ppm的TLV,计算得出的PERC和MC的相互作用阈值分别为25 ppm和135 ppm。二元TCE/PERC混合物的TLV暴露低于10%的显著水平。TCE和MC共同暴露的相互作用阈值分别在50 ppm和175 ppm时达到。这种交互式PBPK模型在职业和环境中溶剂混合物暴露的风险评估中应该具有价值。