Using Zebrafish in Preclinical Drug Studies: Challenges and Opportunities

A. V. Kalueff, M. M. Kotova, A. N. Ikrin, T. O. Kolesnikova
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Abstract

Scientific relevance . Since fiscal and regulatory constraints substantially limit bioscreening in rodent models, a wider implementation of additional alternative models in preclinical studies of medicines is gaining momentum. These alternative models include aquatic vertebrates, such as zebrafish (Danio rerio). Aim. The study aimed to examine zebrafish models in terms of their performance in preclinical studies, their current uses, the challenges and opportunities in the field, and strategic directions for the development of preclinical testing in zebrafish. Discussion. Here, the authors summarise the key zebrafish tests that are currently used to assess a wide range of small molecules for their general and endocrine toxicity and effects on the survival of embryos and larvae. The review discusses the strengths and weaknesses of zebrafish models for preclinical testing of neurotropic agents. Additionally, the authors overview various methodological approaches to improving zebrafish toxicity testing. Overall, the use of zebrafish models is gradually becoming internationally established for laboratory testing of small molecules. Conclusions. A wider implementation of zebrafish models in pharmaceutical research and preclinical testing as an additional alternative to rodents, particularly in Russia, may significantly accelerate the development of novel medicinal products and foster a more comprehensive and adequate assessment of the biological risks associated with chemical substances.
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在临床前药物研究中使用斑马鱼:挑战和机遇
科学相关性。由于财政和监管限制极大地限制了啮齿动物模型的生物筛选,因此在药物临床前研究中更广泛地实施其他替代模型的势头正在增强。这些替代模型包括水生脊椎动物,如斑马鱼(Danio rerio)。的目标。本研究旨在研究斑马鱼模型在临床前研究中的表现、目前的用途、该领域的挑战和机遇,以及斑马鱼临床前测试发展的战略方向。讨论。在这里,作者总结了目前用于评估各种小分子的一般毒性和内分泌毒性以及对胚胎和幼虫存活的影响的关键斑马鱼试验。本文讨论了斑马鱼模型用于神经药物临床前试验的优缺点。此外,作者概述了改善斑马鱼毒性测试的各种方法方法。总的来说,斑马鱼模型的使用正在逐渐成为国际上建立的小分子实验室测试。结论。特别是在俄罗斯,在药物研究和临床前测试中更广泛地使用斑马鱼模型作为啮齿动物的额外替代品,可能会大大加快新型药品的开发,并促进对与化学物质相关的生物风险进行更全面和充分的评估。
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发文量
30
审稿时长
12 weeks
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