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运用毒代动力学-毒效动力学模型识别和预测迟发性死亡。

Identifying and Predicting Delayed Mortality with Toxicokinetic-Toxicodynamic Models.

机构信息

DEBtox Research, Stevensweert, The Netherlands.

出版信息

Environ Toxicol Chem. 2024 May;43(5):1030-1035. doi: 10.1002/etc.5833. Epub 2024 Feb 28.

Abstract

The prevalence of standardized toxicity testing in ecotoxicology has largely obscured the notion that toxicity is a function of time as well. The necessity of considering time is vividly demonstrated by observations of delayed mortality, that is, deaths continue to occur even when animals are no longer exposed to a toxicant. In this contribution, I explore to what extent toxicokinetic-toxicodynamic (TKTD) models from the framework of the General Unified Threshold model for Survival (GUTS) can capture delayed mortality, and to what extent this phenomenon can be predicted from short-term standard tests. I use a previously published data set for fluoroquinolones in Daphnia magna that shows strongly delayed mortality (using immobilization as a proxy for death). The model analysis shows that the GUTS stochastic death models can capture delayed mortality in the complete data set with a long recovery phase, but that the delayed effects would not have been predicted from a 2-day standard test. The study underlines the limited information content of standard acute test designs. Toxicokinetic-toxicodynamic modeling offers a handle on the time aspects of toxicity but cannot always be relied on to provide accurate extrapolations based on severely limited standard tests. The phenomenon of delayed toxicity requires more structured study to clarify its prevalence and impact; I discuss several avenues for further investigation. Environ Toxicol Chem 2024;43:1030-1035. © 2024 SETAC.

摘要

毒理学中标准化毒性测试的盛行在很大程度上掩盖了这样一种观点,即毒性也是时间的函数。即使动物不再接触有毒物质,也会持续发生延迟性死亡,这一观察结果生动地证明了需要考虑时间这一点。在本研究中,我探讨了生存的一般统一阈值模型(GUTS)框架中的毒代动力学-毒效动力学(TKTD)模型在多大程度上可以捕捉延迟性死亡,以及这种现象在多大程度上可以从短期标准测试中预测。我使用了先前发表的关于氟喹诺酮类药物对大型溞的数据集,该数据集显示出强烈的延迟性死亡(使用固定作为死亡的替代物)。模型分析表明,GUTS 随机死亡模型可以用长时间恢复期来捕捉完整数据集的延迟性死亡,但从 2 天的标准测试中无法预测出延迟效应。该研究强调了标准急性测试设计的信息量有限。毒代动力学-毒效动力学模型提供了毒性时间方面的处理方法,但不能总是依赖它根据严重受限的标准测试提供准确的外推。延迟毒性现象需要更系统的研究来澄清其普遍性和影响;我讨论了进一步研究的几个途径。环境毒理化学 2024;43:1030-1035。©2024 SETAC。

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