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Acute behavioral effects of deliriant hallucinogens atropine and scopolamine in adult zebrafish.

Andrey D. Volgin, Oleg A. Yakovlev, Konstantin A. Demin, Polina A. Alekseeva, Allan V. Kalueff

Behavioural Brain Research February 1, 2019 DOI: 10.1016/j.bbr.2018.10.033 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Observational animal study (acute dose-response behavioral experiment) Peer reviewed
Population Adult zebrafish (Danio rerio)
Interventions Atropine Scopolamine
Dose Atropine 60, 90 and 120 mg/L; scopolamine 60, 120, 180 and 240 mg/L
Measures Novel tank test (NTT), light-dark test (LDT), shoaling test
Topics Anxiety
Keywords Atropine Deliriant hallucinogens Locomotion Scopolamine Zebrafish
Key findings Atropine at 90 mg/L mildly increased novel tank locomotor activity, scopolamine at 120 mg/L produced anxiety-like novel tank effects without affecting other behaviors, and both drugs disrupted shoaling behavior. The authors argue these results indicate complex, partially overlapping deliriant-like effects and support zebrafish as a potential screening model for cholinergic deliriants.

Abstract

Atropine and scopolamine are classical muscarinic cholinergic antagonists that exert multiple CNS effects. Belonging to a group of deliriant hallucinogens, these drugs induce delirium-like hallucinations, hyperactivity, altered affective states and amnesia. However, as deliriants remain the least studied group of hallucinogens, their complex and poorly understood profiles necessitate further clinical and preclinical studies. The zebrafish (Danio rerio) is rapidly emerging as a powerful model organism for translational neuropsychopharmacology research. Here, we characterize acute behavioral effects of atropine (60, 90 and 120 mg/L) and scopolamine (60, 120, 180 and 240 mg/L) in adult zebrafish subjected to the novel tank (NTT), light-dark (LDT) and shoaling tests. Overall, atropine at 90 mg/L only mildly increased the NTT locomotor activity, scopolamine at 120 mg/L produced anxiogenic-like NTT effects without affecting other behaviors, and both drugs similarly disrupted zebrafish group behavior in the shoaling test. Collectively, this supports complex and partially overlapping deliriant-like effects of acute atropine and scopolamine in zebrafish. The behavioral sensitivity to these drugs suggests zebrafish as potential screens for cholinergic deliriant psychotropic agents, also necessitating further cross-species in-vivo experimental studies.

Comparable studies

Other preclinical and animal studies on anxiety, most cited first.

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