PUBLICATION

Screening for drugs to reduce zebrafish aggression identifies caffeine and sildenafil

Authors
Gutiérrez, H.C., Vacca, I., Schoenmacker, G., Cleal, M., Tochwin, A., O'Connor, B., Young, A.M.J., Vasquez, A.A., Winter, M.J., Parker, M.O., Norton, W.H.J.
ID
ZDB-PUB-191106-14
Date
2019
Source
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology   30: 17-29 (Journal)
Registered Authors
Norton, Will
Keywords
Aggression, Behaviour, Caffeine, Drug screen, Sildenafil, Zebrafish
MeSH Terms
  • Age Factors
  • Aggression/drug effects*
  • Aggression/physiology
  • Aggression/psychology*
  • Animals
  • Brain/drug effects
  • Brain/metabolism
  • Caffeine/pharmacology*
  • Central Nervous System Stimulants/pharmacology
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical/methods
  • Reaction Time/drug effects*
  • Reaction Time/physiology
  • Sildenafil Citrate/pharmacology*
  • Vasodilator Agents/pharmacology
  • Zebrafish
PubMed
31679888 Full text @ Eur Neuropsychopharmacol
Abstract
Although aggression is a common symptom of psychiatric disorders the drugs available to treat it are non-specific and can have unwanted side effects. In this study we have used a behavioural platform in a phenotypic screen to identify drugs that can reduce zebrafish aggression without affecting locomotion. In a three tier screen of ninety-four drugs we discovered that caffeine and sildenafil can selectively reduce aggression. Caffeine also decreased attention and increased impulsivity in the 5-choice serial reaction time task whereas sildenafil showed the opposite effect. Imaging studies revealed that both caffeine and sildenafil are active in the zebrafish brain, with prominent activation of the thalamus and cerebellum evident. They also interact with 5-HT neurotransmitter signalling. In summary, we have demonstrated that juvenile zebrafish are a suitable model to screen for novel drugs to reduce aggression, with the potential to uncover the neural circuits and signalling pathways that mediate such behavioural effects.
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