Nichols John W, Fitzsimmons Patrick N, Whiteman Frank W
Mid-Continent Ecology Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Duluth, Minnesota, 55804, USA.
Toxicol Sci. 2004 Feb;77(2):219-29. doi: 10.1093/toxsci/kfh032. Epub 2003 Dec 2.
A physiologically based toxicokinetic (PBTK) model for dietary uptake of hydrophobic organic compounds by fish was used to simulate dosing scenarios commonly encountered in experimental and field studies. Simulations were initially generated for the model compound [UL-(14)C] 2,2',5,5'-tetrachlorobiphenyl ([(14)C] PCB 52). Steady-state exposures were simulated by calculating chemical concentrations in tissues of the predator corresponding to an equilibrium distribution between the fish and water (termed the bioconcentration or BCF residue data set). This residue data set was then varied in a proportional manner until whole-body chemical concentrations exhibited no net change for each set of exposure conditions. For [(14)C] PCB 52, the proportional increase in BCF residues (termed the biomagnification factor or BMF) required to achieve steady state in a food-only exposure was 2.24, while in a combined food and water exposure the BMF was 3.11. Additional simulations for the food and water exposure scenario were obtained for a set of hypothetical organic compounds with increasing log K(OW) values. Using gut permeability coefficients determined for [(14)C] PCB 52, predicted BMFs increased with chemical log K(OW), achieving levels much higher than those reported in field sampling efforts. BMFs comparable to measured values were obtained by reducing permeability coefficients within each gut segment in a log K(OW)-dependent manner. This predicted decrease in chemical permeability is consistent with earlier work, suggesting that dietary absorption of hydrophobic compounds by fish is controlled in part by factors that vary with chemical log K(OW). Relatively low rates of metabolism or growth were shown to have a substantial impact on steady-state biomagnification of chemical residues.
一个用于模拟鱼类通过饮食摄取疏水性有机化合物的基于生理的毒代动力学(PBTK)模型,被用来模拟实验和现场研究中常见的给药场景。最初针对模型化合物[UL-(14)C] 2,2',5,5'-四氯联苯([(14)C] PCB 52)进行了模拟。通过计算捕食者组织中的化学浓度来模拟稳态暴露,该浓度对应于鱼和水之间的平衡分布(称为生物浓缩或BCF残留数据集)。然后以成比例的方式改变这个残留数据集,直到每组暴露条件下全身化学浓度没有净变化。对于[(14)C] PCB 52,在仅通过食物暴露达到稳态所需的BCF残留的成比例增加(称为生物放大因子或BMF)为2.24,而在食物和水联合暴露中BMF为3.11。针对一组log K(OW)值不断增加的假设有机化合物,获得了食物和水暴露场景的额外模拟结果。利用针对[(14)C] PCB 52测定的肠道渗透系数,预测的BMF随着化学物质的log K(OW)增加,达到的水平远高于现场采样研究中报告的水平。通过以log K(OW)依赖的方式降低每个肠道段内的渗透系数,获得了与测量值相当的BMF。这种预测的化学物质渗透性降低与早期工作一致,表明鱼类对疏水性化合物的饮食吸收部分受随化学物质log K(OW)变化的因素控制。相对较低的代谢或生长速率被证明对化学残留物的稳态生物放大有重大影响。