Zebrafishlab, Veterinary Physiology and Biochemistry, Department of Veterinary Sciences, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium.
Zebrafishlab, Veterinary Physiology and Biochemistry, Department of Veterinary Sciences, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium; Systemic Physiological and Ecotoxicological Research (SPHERE), Department of Biology, University of Antwerp, Groenenborgerlaan 171, 2020 Antwerp, Belgium.
Aquat Toxicol. 2018 Jul;200:1-12. doi: 10.1016/j.aquatox.2018.04.009. Epub 2018 Apr 21.
The adverse outcome pathway (AOP) framework can be used to help support the development of alternative testing strategies aimed at predicting adverse outcomes caused by triggering specific toxicity pathways. In this paper, we present a case-study demonstrating the selection of alternative in chemico assays targeting the molecular initiating events of established AOPs, and evaluate use of the resulting data to predict higher level biological endpoints. Based on two AOPs linking inhibition of the deiodinase (DIO) enzymes to impaired posterior swim bladder inflation in fish, we used in chemico enzyme inhibition assays to measure the molecular initiating events for an array of 51 chemicals. Zebrafish embryos were then exposed to 14 compounds with different measured inhibition potentials. Effects on posterior swim bladder inflation, predicted based on the information captured by the AOPs, were evaluated. By linking the two datasets and setting thresholds, we were able to demonstrate that the in chemico dataset can be used to predict biological effects on posterior chamber inflation, with only two outliers out of the 14 tested compounds. Our results show how information organized using the AOP framework can be employed to develop or select alternative assays, and successfully forecast downstream key events along the AOP. In general, such in chemico assays could serve as a first-tier high-throughput system to screen and prioritize chemicals for subsequent acute and chronic fish testing, potentially reducing the need for long-term and costly toxicity tests requiring large numbers of animals.
不良结局途径(AOP)框架可用于支持开发旨在预测特定毒性途径引发的不良结局的替代测试策略。在本文中,我们展示了一个案例研究,该研究演示了针对既定 AOP 的分子起始事件选择替代化学分析方法,并评估了使用这些数据预测更高水平生物学终点的情况。基于将脱碘酶(DIO)酶抑制与鱼类后游泳囊充气受损联系起来的两个 AOP,我们使用化学抑制测定法来测量 51 种化学物质的分子起始事件。然后,将斑马鱼胚胎暴露于 14 种具有不同测量抑制潜力的化合物中。根据 AOP 捕获的信息预测对后游泳囊充气的影响。通过将两个数据集联系起来并设置阈值,我们能够证明化学数据集可用于预测对后腔充气的生物学影响,在测试的 14 种化合物中只有两种异常值。我们的结果表明,如何使用 AOP 框架组织信息可以用于开发或选择替代测定方法,并成功预测 AOP 中的下游关键事件。通常,此类化学分析方法可以作为一种用于筛选和优先考虑化学物质的高通量系统,用于随后的急性和慢性鱼类测试,从而可能减少对需要大量动物的长期和昂贵毒性测试的需求。