4.7 Article

Acute Administration of Ethanol and of a D1-Receptor Antagonist Affects the Behavior and Neurochemistry of Adult Zebrafish

Journal

BIOMEDICINES
Volume 10, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/biomedicines10112878

Keywords

alcohol abuse; alcoholism; ethanol; ethyl alcohol; dopamine; shoaling; zebrafish

Funding

  1. NSERC (Canada) [311637]
  2. University of Toronto Mississauga Distinguished Professorship Award
  3. UTM Provostial Grant

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This study investigates the effects of acute alcohol administration in zebrafish, suggesting that alcohol may influence behavior through dopaminergic mechanisms. Significant interactions and main effects of alcohol and D1-R antagonist are found on behavioral phenotypes and neurochemical levels, hinting at potential strain differences in identifying molecular mechanisms underlying acute alcohol effects.
Alcohol abuse represents major societal problems, an unmet medical need resulting from our incomplete understanding of the mechanisms underlying alcohol's actions in the brain. To uncover these mechanisms, animal models have been proposed. Here, we explore the effects of acute alcohol administration in zebrafish, a promising animal model in alcohol research. One mechanism via which alcohol may influence behavior is the dopaminergic neurotransmitter system. As a proof-of-concept analysis, we study how D1 dopamine-receptor antagonism may alter the effects of acute alcohol on the behavior of adult zebrafish and on whole brain levels of neurochemicals. We conduct these analyses using a quasi-inbred strain, AB, and a genetically heterogeneous population SFWT. Our results uncover significant alcohol x D1-R antagonist interaction and main effects of these factors in shoaling, but only additive effects of these factors in measures of exploratory behavior. We also find interacting and main effects of alcohol and the D1-R antagonist on dopamine and DOPAC levels, but only alcohol effects on serotonin. We also uncover several strain dependent effects. These results demonstrate that acute alcohol may act through dopaminergic mechanisms for some but not all behavioral phenotypes, a novel discovery, and also suggest that strain differences may, in the future, help us identify molecular mechanisms underlying acute alcohol effects.

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