Aug 2026· Biomolecules· Vol 16, pp. 1230· 0 citations· 71 references
Medicine
TL;DR
The behavioral effects of ketamine are presented and the methodologies used in the search for novel rapid-acting antidepressant drugs (RAADs) are discussed, which inspired a new model for the search for rapid-acting ketamine-like antidepressants.
Abstract
The use of animal models to study mental illnesses, such as depression, requires proper standardization and extensive expertise. Achieving good construct, face, and predictive validity in depression models is quite challenging. Currently, only a few environmental models, mostly based on chronic stress, and a limited number of genetic models fulfill these criteria. In the quest for new antidepressants, initial screening tests are employed as a preliminary step in research. While these tests do not always meet the requirements of a disease model, they are useful for the early identification of substances that may have antidepressant potential, paving the way for further studies based on established models. This approach to discovering antidepressants was originally designed for traditional medications, which typically act by modulating serotonergic, noradrenergic, and dopaminergic systems, and require multi-week administration to produce a therapeutic effect. In contrast, the new antidepressant ketamine offers rapid therapeutic effects following a single dose and exhibits distinctive behavioral outcomes in both screening tests and animal depression models. These effects have inspired a new model for the search for rapid-acting ketamine-like antidepressants. This review presents the behavioral effects of ketamine and discusses the methodologies used in the search for novel rapid-acting antidepressant drugs (RAADs).
A synthesis of animal models of depression, including stress paradigms, developmental and genetic models, neuroendocrine manipulations, immune-based, metabolic and hormone-related models, are provided.
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A comprehensive and updated overview of the principal experimental models of depression in mice and rats, including stress-based (learned helplessness, chronic unpredictable mild stress, early-life stress, early-life stress, and social defeat), surgical, pharmacological, and genetic models are provided.
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