Program in Biology, New York University Abu Dhabi, Saadiyat Island, United Arab Emirates.
Curr Protoc. 2021 Sep;1(9):e231. doi: 10.1002/cpz1.231.
The use of whole animal models in toxicological studies is essential for understanding the physiological responses caused by chemical exposures. However, such studies can face reproducibility challenges due to unaccounted experimental parameters that can have a marked influence on toxicological outcomes. Zebrafish embryos and larvae are a popular vertebrate animal model for studying cellular, tissue, and organ responses to toxicant exposures. Despite the popularity of this system, standardized protocols that control for the influence of various experimental parameters and culture conditions on the toxicological response in these animals have not been widely adopted, making it difficult to compare findings from different laboratories. Here, we describe a detailed approach for designing and optimizing protocols to assess the impact of chemical exposures on the development and survival of zebrafish embryos and larvae. We first describe our standard procedure to determine two key toxicological thresholds, the maximum tolerable concentration (MTC) and the lethal concentration (LC , defined as that in which 50% of larvae die), in response to an exposure that persists from early development through larval maturation. We then describe two protocols to systematically test how key experimental parameters, including genetic background, culture media, animal density, volume, plate material, and developmental stage in which the embryos are exposed, alter the MTC and LC . Finally, we provide a step-by-step guide to assess the interaction between two chemicals using this model. These protocols will guide the standardization of toxicological studies using zebrafish and maximize reproducibility. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Zebrafish embryo collection and culture, and establishment of the MTC and LC Basic Protocol 2: Evaluation of the impact of culture conditions on toxicant responses of zebrafish embryo and larvae Basic Protocol 3: Identification of the developmental window of sensitivity to toxicant exposure Basic Protocol 4: Testing interaction between multiple toxicants.
在毒理学研究中使用整体动物模型对于理解化学暴露引起的生理反应至关重要。然而,由于未考虑到对毒理学结果有显著影响的实验参数,此类研究可能会面临可重复性挑战。斑马鱼胚胎和幼虫是研究细胞、组织和器官对毒物暴露反应的一种常用脊椎动物动物模型。尽管该系统很受欢迎,但尚未广泛采用标准化方案来控制各种实验参数和培养条件对这些动物毒理学反应的影响,这使得难以比较不同实验室的研究结果。在这里,我们描述了一种详细的方法,用于设计和优化方案,以评估化学暴露对斑马鱼胚胎和幼虫发育和存活的影响。我们首先描述了我们确定两个关键毒理学阈值(最大耐受浓度(MTC)和致死浓度(LC,定义为 50%幼虫死亡的浓度)的标准程序,以应对从早期发育到幼虫成熟持续暴露的情况。然后,我们描述了两种方案,以系统地测试包括遗传背景、培养基、动物密度、体积、板材料以及暴露胚胎的发育阶段在内的关键实验参数如何改变 MTC 和 LC。最后,我们提供了使用该模型评估两种化学物质相互作用的分步指南。这些方案将指导使用斑马鱼进行毒理学研究的标准化,并最大限度地提高可重复性。