Ketamine-induced NMDA receptor hypofunction alters social and locomotor behavior in adult zebrafish
Matheus Gallas‐lopes, Dagobert Müller, Thailana Stahlhofer-Buss, Leonardo M. Bastos, Sofia Z. Becker, Samara Machado Bruck, Ângelo Piato, Ana Paula Herrmann
bioRxiv (Cold Spring Harbor Laboratory) September 17, 2025 preprint DOI: 10.1101/2025.09.16.676572 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Experimental study |
|---|---|
| Population | Adult zebrafish |
| Intervention | Ketamine |
| Dose | 10, 20, or 40 mg/L |
| Duration | 5-day or 14-day exposure, with testing 48 hours after final treatment |
| Topics | Ketamine Esketamine |
| Keywords | Neurochemical Zebrafish Nmda receptor Locomotor activity Behavioral sensitization Animal model Antipsychotic Psychosis Schizophrenia object-oriented programming Model organism Behavioral syndrome Fish <actinopterygii> Escape response Rodent Pharmacology |
| Key findings | Ketamine induced acute, concentration-dependent reductions in social interaction and increases in locomotor activity and rotational behavior in zebrafish, but these effects did not sensitize with repeated exposure or persist after a 48-hour washout. |
Abstract
ABSTRACT Background NMDA receptor antagonists, such as ketamine, are widely used to model schizophrenia-related phenotypes in preclinical studies. While zebrafish have emerged as a promising model organism for neuropsychiatric research, few studies have characterized their behavioral responses to repeated ketamine exposure.
Methods: Three independent experiments were conducted to evaluate the acute, repeated and sustained behavioral effects of ketamine in adult zebrafish. In Experiment I, fish were exposed to 10, 20, or 40 mg/L ketamine once daily for five days, and submitted to the social preference (SPT) and open tank (OTT) tests on days 1 and 5, and re-exposed and re-tested on day 7 after a 48-hour washout. Experiments II and III assessed whether behavioral changes persisted following 5- or 14-day exposure protocols, with testing conducted 48 hours after the final treatment.
Results: Ketamine induced robust, concentration-dependent alterations in Experiment I: it reduced social interaction and increased locomotor activity in the SPT on all experimental days, while increased rotational behavior in the OTT on days 1 and 5. These effects did not intensify over repeated exposure and were not sustained after a 48-hour washout in either protocol (Experiments II and III).
Conclusions: The results support the utility of zebrafish for modeling acute behavioral responses to NMDA receptor antagonism, capturing features of schizophrenia-like phenotypes. However, no evidence of behavioral sensitization or lasting disruption was observed, diverging from rodent studies. Future studies should incorporate antipsychotic validation, neurochemical analyses, and alternative exposure strategies to further develop zebrafish as a translational model for psychiatric research.
Comparable studies
Other preclinical and animal studies on ketamine, most cited first.
| Study | Year | Design | Participants |
|---|---|---|---|
| mTOR-Dependent Synapse Formation Underlies the Rapid Antidepressant Effects of NMDA Antagonists Rats | 2010 | Observational study | |
| Activation of Glutamatergic Neurotransmission by Ketamine: A Novel Step in the Pathway from NMDA Receptor Blockade to Dopaminergic and Cognitive Disruptions Associated with the Prefrontal Cortex Conscious rats | 1997 | Dose-response study with microdialysis and behavioral testing | |
| NMDAR inhibition-independent antidepressant actions of ketamine metabolites Mice | 2016 | Preclinical study | |
| The dissociative anaesthetics, ketamine and phencyclidine, selectively reduce excitation of central mammalian neurones by N‐methyl‐aspartate Spinal neurons in decerebrate or pentobarbitone-anaesthetized cats and rats | 1983 | Experimental study | |
| R-ketamine: a rapid-onset and sustained antidepressant without psychotomimetic side effects Mice | 2015 | Experimental study |
Citations in the library
Cites 14
- Ketamine-Induced Loss of Phenotype of Fast-Spiking Interneurons Is Mediated by NADPH-Oxidase Science December 6, 2007
- Reviewing the ketamine model for schizophrenia Journal of Psychopharmacology November 20, 2013
- Is the Acute NMDA Receptor Hypofunction a Valid Model of Schizophrenia? Schizophrenia Bulletin September 28, 2011
- Rodent ketamine depression-related research: Finding patterns in a literature of variability Behavioural Brain Research August 13, 2019
- Glutamate NMDA Receptor Antagonists with Relevance to Schizophrenia: A Review of Zebrafish Behavioral Studies. Current Neuropharmacology March 4, 2022
and 9 more in the library