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Development Features on the Selection of Animal Models for Teratogenic Testing
Sofia Alves-Pimenta1,2, Bruno Colaço1,2, Paula A Oliveira2,3,4,5
1Department of Animal Science, School of Agrarian and Veterinary Sciences (CECAV), University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal.
Methods in Molecular Biology (Clifton, N.J.)
|January 29, 2024
Summary
Animal models are crucial for teratogenic testing, with invertebrates and non-mammalian vertebrates offering efficient, ethical screening. Understanding developmental pathways optimizes compound safety and market speed.
Area of Science:
- Developmental toxicology
- Comparative embryology
- Animal model systems
Background:
- Animal models are essential for teratogenic testing of new substances.
- Similar developmental processes in animals aid human safety assessments.
- Embryology advances highlight sensitivity to toxicity during development.
Purpose of the Study:
- Outline essential developmental periods in various animal models for teratogenic testing.
- Compare species' similarities, differences, advantages, and disadvantages.
- Highlight specific sensitivities for teratogenic testing across models.
Main Methods:
- Categorize animal models into invertebrate, non-mammalian vertebrate, and mammalian species.
- Detail specific examples within each category (e.g., Eisenia fetida, Xenopus laevis, Mus musculus).
- Discuss regulatory requirements and the increasing use of alternative models.
Main Results:
- Invertebrates (e.g., Eisenia fetida, C. elegans, D. melanogaster) offer rapid results and fewer ethical concerns.
- Non-mammalian vertebrates (e.g., Xenopus laevis, Danio rerio) assess later development with reduced ethical demands.
- Mammals (e.g., Mus musculus, Rattus norvegicus) are vital for complex, late-stage development but face ethical and cost limitations for screening.
Conclusions:
- Invertebrate and non-mammalian vertebrate models are valuable for high-throughput screening due to cost-effectiveness and ethical advantages.
- Improved understanding of developmental pathways enhances human translation and reduces animal use.
- Optimized animal model selection improves compound safety profiles and accelerates market entry.
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