Protocols for the Evaluation of Neurodevelopmental Alterations in Rabbit Models and .

Front Toxicol

BCNatal-Barcelona Center for Maternal-Fetal and Neonatal Medicine (Hospital Clínic and Hospital Sant Joan de Déu), Fetal i+D Fetal Medicine Research Center, IDIBAPS, University of Barcelona, Center for Biomedical Research on Rare Diseases (CIBER-ER), Barcelona, Spain.

Published: July 2022

AI Article Synopsis

  • - The rabbit model is increasingly valued in neurodevelopmental studies due to its closer resemblance to human brain development compared to rodents.
  • - The publication outlines 14 detailed protocols focusing on various toxicological endpoints to evaluate neurodevelopmental adverse effects in rabbits, spanning from the neonatal phase to long-term assessments.
  • - Each protocol includes expected control values, troubleshooting tips, and addresses techniques like neurosphere assays, behavioral tests, and neurohistopathological evaluations, making it a thorough resource for researchers.

Article Abstract

The rabbit model is gaining importance in the field of neurodevelopmental evaluation due to its higher similarity to humans in terms of brain development and maturation than rodents. In this publication, we detailed 14 protocols covering toxicological relevant endpoints for the assessment of neurodevelopmental adverse effects in the rabbit species. These protocols include both and techniques, which also cover different evaluation time-points, the neonatal period, and long-term examinations at postnatal days (PNDs) 50-70. Specifically, the protocols (P) included are as follows: neurosphere preparation (GD30/PND0; P2) and neurosphere assay (P3), behavioral ontogeny (PND1; P4), brain obtaining and brain weight measurement at two different ages: PND1 (P5) and PND70 (P12), neurohistopathological evaluations after immersion fixation for neurons, astrocytes, oligodendrocytes and microglia (PND1; P6-9) or perfusion fixation (PND70; P12), motor activity (P11, open field), memory and sensory function (P11, object recognition test), learning (P10, Skinner box), and histological evaluation of plasticity (P13 and P14) through dendritic spines and perineuronal nets. The expected control values and their variabilities are presented together with the information on how to troubleshoot the most common issues related to each protocol. To sum up, this publication offers a comprehensive compilation of reliable protocols adapted to the rabbit model for neurodevelopmental assessment in toxicology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9355155PMC
http://dx.doi.org/10.3389/ftox.2022.918520DOI Listing

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