Ramhøj Louise, Axelstad Marta, Baert Yoni, Cañas-Portilla Ana I, Chalmel Frédéric, Dahmen Lars, De La Vieja Antonio, Evrard Bertrand, Haigis Ann-Cathrin, Hamers Timo, Heikamp Kim, Holbech Henrik, Iglesias-Hernandez Patricia, Knapen Dries, Marchandise Lorna, Morthorst Jane E, Nikolov Nikolai Georgiev, Nissen Ana C V E, Oelgeschlaeger Michael, Renko Kostja, Rogiers Vera, Schüürmann Gerrit, Stinckens Evelyn, Stub Mette H, Torres-Ruiz Monica, Van Duursen Majorie, Vanhaecke Tamara, Vergauwen Lucia, Wedebye Eva Bay, Svingen Terje
Research Group for Molecular and Reproductive Toxicology, National Food Institute, Technical University of Denmark, Kgs. Lyngby, Denmark.
Department In Vitro Toxicology and Dermato-cosmetology (IVTD), Vrije Universiteit Brussel, Jette, Belgium.
Front Toxicol. 2023 May 17;5:1189303. doi: 10.3389/ftox.2023.1189303. eCollection 2023.
Current test strategies to identify thyroid hormone (TH) system disruptors are inadequate for conducting robust chemical risk assessment required for regulation. The tests rely heavily on histopathological changes in rodent thyroid glands or measuring changes in systemic TH levels, but they lack specific new approach methodologies (NAMs) that can adequately detect TH-mediated effects. Such alternative test methods are needed to infer a causal relationship between molecular initiating events and adverse outcomes such as perturbed brain development. Although some NAMs that are relevant for TH system disruption are available-and are currently in the process of regulatory validation-there is still a need to develop more extensive alternative test batteries to cover the range of potential key events along the causal pathway between initial chemical disruption and adverse outcomes in humans. This project, funded under the Partnership for the Assessment of Risk from Chemicals (PARC) initiative, aims to facilitate the development of NAMs that are specific for TH system disruption by characterizing mechanisms of action that can be targeted by testing strategies. We will develop and improve human-relevant test systems to capture effects on important areas of the TH system. Furthermore, we will elaborate on important species differences in TH system disruption by incorporating non-mammalian vertebrate test species alongside classical laboratory rat species and human-derived assays.
当前用于识别甲状腺激素(TH)系统干扰物的测试策略,不足以进行监管所需的可靠化学风险评估。这些测试严重依赖啮齿动物甲状腺的组织病理学变化或测量全身TH水平的变化,但它们缺乏能够充分检测TH介导效应的特定新方法(NAMs)。需要此类替代测试方法来推断分子起始事件与诸如脑发育受扰等不良后果之间的因果关系。尽管有一些与TH系统干扰相关的NAMs可供使用,且目前正处于监管验证过程中,但仍需要开发更广泛的替代测试组合,以涵盖从最初的化学干扰到人类不良后果的因果途径中一系列潜在关键事件。该项目由化学品风险评估伙伴关系(PARC)倡议资助,旨在通过表征可被测试策略靶向的作用机制,推动开发针对TH系统干扰的NAMs。我们将开发并改进与人类相关的测试系统,以捕捉对TH系统重要区域的影响。此外,我们将通过纳入非哺乳动物脊椎动物测试物种以及经典实验大鼠物种和人类衍生试验,阐述TH系统干扰中重要的物种差异。