Murray F Jay, Roth Randy N, Nicolich Mark J, Gray Thomas M, Simpson Barry J
Murray & Associates, 5529 Perugia Circle, San Jose, CA 95138, USA.
Regul Toxicol Pharmacol. 2013 Nov 1;67(2 Suppl):S46-59. doi: 10.1016/j.yrtph.2013.05.003. Epub 2013 May 13.
In response to the US EPA HPV Challenge Program, this study was conducted to: (1) evaluate the relationship between PAC content and the developmental toxicity of high-boiling petroleum substances (HBPS) and (2) develop mathematical models to predict the developmental toxicity of similar untested substances based on their aromatic ring class (ARC) profiles. For this investigation, 68 developmental toxicity studies were reviewed. The ARC models relied on data from 21 rat dermal developmental toxicity studies conducted with similar experimental designs to ensure a consistent data set for comparison. The most sensitive general endpoints of developmental toxicity (i.e., decreased fetal survival and growth) were chosen for modeling. The ARC models demonstrated a strong correlation between the predicted vs. observed values for specific sensitive endpoints of these developmental toxicities (percent resorptions, r=0.99; live fetuses per litter, r=0.98; fetal body weight, r=0.94). Such associations provide a promising approach for predicting the developmental toxicity of untested HBPS. Efforts to corroborate the ARC models using test substances that were not used to build the ARC models produced mixed results, and further development and refinement of the ARC models is recommended before they can be reliably applied to all HBPS.
针对美国环境保护局(EPA)的人类乳头瘤病毒(HPV)挑战计划,开展了本研究,目的是:(1)评估多环芳烃(PAC)含量与高沸点石油物质(HBPS)发育毒性之间的关系;(2)基于其芳香环类别(ARC)概况,建立数学模型以预测类似未测试物质的发育毒性。为此项调查,回顾了68项发育毒性研究。ARC模型依赖于21项大鼠皮肤发育毒性研究的数据,这些研究采用了相似的实验设计,以确保有一组一致的数据集用于比较。选择发育毒性最敏感的一般终点(即胎儿存活率和生长率降低)进行建模。ARC模型显示,这些发育毒性特定敏感终点的预测值与观察值之间存在很强的相关性(吸收百分比,r = 0.99;每窝活胎数,r = 0.98;胎儿体重,r = 0.94)。这种关联为预测未测试的HBPS的发育毒性提供了一种有前景的方法。使用未用于构建ARC模型的测试物质来确证ARC模型的努力产生了混合结果,建议在ARC模型能够可靠地应用于所有HBPS之前,对其进行进一步开发和完善。