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敏感性分析在大鼠四氯化碳生理药代动力学模型中的应用。

Applications of sensitivity analysis to a physiologically based pharmacokinetic model for carbon tetrachloride in rats.

作者信息

Evans M V, Crank W D, Yang H M, Simmons J E

机构信息

PKB/ETD/HERL United States Environmental Protection Agency, Research Triangle Park, North Carolina 27711.

出版信息

Toxicol Appl Pharmacol. 1994 Sep;128(1):36-44. doi: 10.1006/taap.1994.1177.

Abstract

Physiologically based pharmacokinetic (PBPK) models developed from gas uptake experiments have been used to estimate metabolic parameters for volatile organic compounds. Due to the potential application of PBPK models to estimate metabolic bioactivation constants in humans, it is important to understand the complex nature of these models and the resulting estimates. Adult male F344 rats (165-205 g) were individually exposed to carbon tetrachloride (CCl4) in gas uptake systems. Three rats at each concentration were exposed for 6 hr to initial concentrations of 25, 100, 250, and 1000 ppm CCl4. Partition coefficient determinations were performed by the vial equilibration technique and used as model inputs. Computer optimizations with the means of each initial chamber concentration at each time point resulted in an estimate of Vmax of 0.11 mg/hr (Vmaxc = 0.37 mg/hr/kg) and Km of 1.3 mg/liter. To determine the effect of individual animal variation in Vmax, optimizations were also performed with the mean +/- SD, resulting in Vmax estimates of 0.09 and 0.12 mg/hr, respectively. Similar analysis resulted in Km estimates of 0.98 and 1.58 mg/liter. The results of the sensitivity analysis were concentration dependent for CCl4. These results show Vmax and Km to be most accurately detected at lower initial chamber concentrations. Results of the sensitivity analysis at the lowest concentration established the following model input hierarchy: blood to air partition > fat partition and fat volume fraction > slowly perfused partition, ventilation rate, cardiac output, fat blood flow percentage > liver blood flow percentage and slowly perfused blood flow percentage. Further sensitivity analysis determined Vmax and Km to be highly correlated when using gas uptake technology and point to the need to an independent estimate for either constant. In summary, the application of sensitivity analysis to PBPK modeling resulted in an increased understanding of factors governing the estimation of metabolic parameters.

摘要

基于气体摄取实验建立的生理药代动力学(PBPK)模型已被用于估算挥发性有机化合物的代谢参数。由于PBPK模型在估算人体代谢生物活化常数方面的潜在应用,了解这些模型的复杂性质以及由此产生的估算值非常重要。成年雄性F344大鼠(165 - 205克)在气体摄取系统中分别暴露于四氯化碳(CCl4)。每个浓度下的三只大鼠暴露于25、100、250和1000 ppm CCl4的初始浓度6小时。通过小瓶平衡技术进行分配系数测定,并将其用作模型输入。在每个时间点对每个初始腔室浓度的平均值进行计算机优化,得出Vmax估计值为0.11毫克/小时(Vmaxc = 0.37毫克/小时/千克),Km为1.3毫克/升。为了确定个体动物Vmax变化的影响,还使用平均值±标准差进行了优化,得出Vmax估计值分别为0.09和0.12毫克/小时。类似分析得出Km估计值为0.98和1.58毫克/升。四氯化碳的敏感性分析结果与浓度有关。这些结果表明,在较低的初始腔室浓度下,Vmax和Km能被最准确地检测到。最低浓度下的敏感性分析结果确定了以下模型输入层次结构:血 - 气分配系数>脂肪分配系数和脂肪体积分数>缓慢灌注分配系数、通气率、心输出量、脂肪血流量百分比>肝血流量百分比和缓慢灌注血流量百分比。进一步的敏感性分析表明,使用气体摄取技术时,Vmax和Km高度相关,这表明需要对任一常数进行独立估计。总之,将敏感性分析应用于PBPK建模有助于加深对控制代谢参数估算因素的理解。

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