4.6 Article

Effects of acute and chronic arecoline in adult zebrafish: Anxiolytic-like activity, elevated brain monoamines and the potential role of microglia

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pnpbp.2020.109977

Keywords

Zebrafish; Arecoline; CNS; Anxiety; Genomic effects

Funding

  1. Southwest University Zebrafish Platform Construction Funds
  2. Special Rector's Productivity Fellowship for SPSU PhD Students
  3. Russian Science Foundation [19-15-00053]
  4. St. Petersburg State University (St. Petersburg, Russia) [51130521]
  5. Institute of Physiology and Basic Medicine (Novosibirsk, Russia) [AAAA-A16-116021010228-0]
  6. St. Petersburg State University [51143531]
  7. Russian Science Foundation [19-15-00053] Funding Source: Russian Science Foundation

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Arecoline is a naturally occurring psychoactive alkaloid with effects on nicotinic and muscarinic receptors. Studies on zebrafish showed that acute and chronic arecoline treatments induced anxiolytic-like behavior, altered neurotransmitter levels, and activated specific genes related to brain function and immune response, suggesting potential for developing novel anxiolytic drugs based on arecoline-like molecules.
Arecoline is a naturally occurring psychoactive alkaloid with partial agonism at nicotinic and muscarinic acetylcholine receptors. Arecoline consumption is widespread, making it the fourth (after alcohol, nicotine and caffeine) most used substance by humans. However, the mechanisms of acute and chronic action of arecoline in-vivo remain poorly understood. Animal models are a valuable tool for CNS disease modeling and drug screening. Complementing rodent studies, the zebrafish (Danio rerio) emerges as a promising novel model organism for neuroscience research. Here, we assessed the effects of acute and chronic arecoline on adult zebrafish behavior and physiology. Overall, acute and chronic arecoline treatments produced overt anxiolytic-like behavior (without affecting general locomotor activity and whole-body cortisol levels), with similar effects also caused by areca nut water extracts. Acute arecoline at 10 mg/L disrupted shoaling, increased social preference, elevated brain norepinephrine and serotonin levels and reduced serotonin turnover. Acute arecoline also upregulated early protooncogenes c-fos and c-jun in the brain, whereas chronic treatment with 1 mg/L elevated brain expression of microglia-specific biomarker genes egr2 and ym1 (thus, implicating microglial mechanisms in potential effects of long-term arecoline use). Finally, acute 2-h discontinuation of chronic arecoline treatment evoked withdrawal-like anxiogenic behavior in zebrafish. In general, these findings support high sensitivity of zebrafish screens to arecoline and related compounds, and reinforce the growing utility of zebrafish for probing molecular mechanisms of CNS drugs. Our study also suggests that novel anxiolytic drugs can eventually be developed based on arecoline-like molecules, whose integrative mechanisms of CNS action may involve monoaminergic and neuro-immune modulation.

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