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Alcohol-induced behavioral changes in zebrafish: The role of dopamine D2-like receptors.
- Source :
-
Psychopharmacology [Psychopharmacology (Berl)] 2016 Jun; Vol. 233 (11), pp. 2119-2128. Date of Electronic Publication: 2016 Mar 09. - Publication Year :
- 2016
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Abstract
- Rationale: The dopaminergic system has been proposed to mediate alcohol-induced locomotor activity, yet the mechanisms underlying this behavioral response remain poorly understood.<br />Objectives: This study was conducted to investigate the role of dopamine D2-like receptors in mediating alcohol-induced behavioral responses.<br />Methods: In experiment 1, we examined the effects of high concentrations (0, 2.5, 5, 10 μM) of haloperidol on motor responses. In experiment 2, we examined the effects of low concentrations (0, 0.625, 1.25, 2.5 μM) of haloperidol on anxiety-like behavioral responses using the novel tank test. In experiment 3, we examined the effect of pre-treating zebrafish with different concentrations of haloperidol (0, 0.625, 2.5 μM) and subsequently exposing them to 0 or 1 % alcohol.<br />Results: In experiment 1, haloperidol induced an inverted U-shaped concentration-dependent increase in locomotor activity. In experiment 2, haloperidol (2.5 μM) reduced the absolute turn angle and freezing behavior in a new environment. In experiment 3, acute alcohol exposure significantly increased locomotor activity and decreased anxiety-like behavioral responses. Pre-treating zebrafish with the lower dose of haloperidol (0.625 μM) abolished the alcohol-induced locomotor activity, without altering anxiety-like behavioral responses. However, pre-treating with the higher dose of haloperidol (2.5 μM) abolished both alcohol-induced increase of locomotor activity and reduction of anxiety-like behavioral responses.<br />Conclusion: The results suggest alcohol-induced locomotor hyperactivity in zebrafish is mediated via activation of dopamine D2-like receptors, whereas anxiety-like behavioral responses may only be altered by a high haloperidol concentration, at which dose the drug may affect receptors other than D2-R.
- Subjects :
- Animals
Anti-Anxiety Agents pharmacology
Anxiety chemically induced
Anxiety psychology
Central Nervous System Depressants antagonists & inhibitors
Dopamine Antagonists pharmacology
Dose-Response Relationship, Drug
Ethanol antagonists & inhibitors
Haloperidol antagonists & inhibitors
Haloperidol pharmacology
Locomotion drug effects
Motor Activity drug effects
Behavior, Animal drug effects
Central Nervous System Depressants pharmacology
Ethanol pharmacology
Receptors, Dopamine D2 drug effects
Zebrafish physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1432-2072
- Volume :
- 233
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Psychopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 26955840
- Full Text :
- https://doi.org/10.1007/s00213-016-4264-3