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The Non-Peptide Arginine-Vasopressin v1a Selective Receptor Antagonist, SR49059, Blocks the Rewarding, Prosocial, and Anxiolytic Effects of 3,4-Methylenedioxymethamphetamine and Its Derivatives in Zebra Fish

Bibliographic Data

ID15522700
AuthorsLuisa Ponzoni (0000-0002-0652-0766, Fondazione Umberto Veronesi), Daniela Braida (0000-0002-5867-1902, University of Milan), Gianpietro Bondiolotti (0000-0002-0872-6725, University of Milan), Mariaelvina Sala (0000-0001-9310-958X, National Research Council, corresponding author)
Year2017
Volume8
Pages146-146
Publication date2017-08-13
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2017.00146
PMID28855876
OpenAlexW2740318118
LanguageEN
Citations received1
References cited6

3,4-Methylenedioxymethamphetamine (MDMA) and its derivatives, 2,5-dimethoxy-4-bromo-amphetamine hydrobromide (DOB) and para -methoxyamphetamine (PMA), are recreational drugs whose pharmacological effects have recently been attributed to serotonin 5HT 2A/C receptors. However, there is growing evidence that the oxytocin (OT)/vasopressin system can modulate some the effects of MDMA. In this study, MDMA (2.5-10 mg/kg), DOB (0.5 mg/kg), or PMA (0.005, 0.1, or 0.25 mg/kg) were administered intramuscularly to adult zebra fish, alone or in combination with the V 1a vasopressin antagonist, SR49059 (0.01-1 ng/kg), before carrying out conditioned place preference (CPP), social preference, novel tank diving, and light-dark tests in order to evaluate subsequent rewarding, social, and emotional-like behavior. The combination of SR49059 and each drug progressively blocked: (1) rewarding behavior as measured by CPP in terms of time spent in drug-paired compartment; (2) prosocial effects measured on the basis of the time spent in the proximity of a nacre fish picture; and (3) anxiolytic effects in terms of the time spent in the upper half of the novel tank and in the white compartment of the tank used for the light-dark test. Antagonism was obtained at SR49059 doses which, when given alone, did not change motor function. In comparison with a control group, receiving vehicle alone, there was a three to five times increase in the brain release of isotocin (the analog of OT in fish) after treatment with the most active doses of MDMA (10 mg/kg), DOB (0.5 mg/kg), and PMA (0.1 mg/kg) as evaluated by means of bioanalytical reversed-phase high-performance liquid chromatography. Taken together, these findings show that the OT/vasopressin system is involved in the rewarding, prosocial, and anxiolytic effects of MDMA, DOB, and PMA in zebra fish and underline the association between this system and the behavioral alterations associated with disorders related to substance abuse

5-HT receptor · Amphetamine · Antagonist · Anxiolytic · Dopamine · MDMA · Neuropeptide · Oxytocin · Receptor · Receptor antagonist · Serotonin · Vasopressin · Medicine · Memory and Neural Mechanisms · Neuroendocrine regulation and behavior · Neuroscience · Psychology · Zebrafish Biomedical Research Applications · Internal Medicine · Pharmacology

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Citations per year0.25
Citation span2022 - 2022 (1)
Highly citedNo

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