Abstract

The behavioural impacts of prenatal exposure to ethanol include a lower IQ, learning problems, anxiety and conduct disorders. Several components of the neurochemical network could contribute to the long-lasting effects of ethanol embryonic exposure. Adenosine is an important neuromodulator, that has been indicated to be affected by acute and chronic exposure to ethanol. Here, embryos of zebrafish exposed to 1% ethanol during the developmental stages of gastrula/segmentation or pharyngula exhibited anxiolytic effect, increased aggressiveness, and decreased social interaction. The exposure during pharyngula stage was able to affect all behavioural parameters analysed at 3 months-post fertilization (mpf), while the treatment during gastrula stage affected the anxiety and social interaction parameters. The aggressiveness was the only behavioural effect of early ethanol exposure that lasted to 12 mpf. The use of a specific inhibitor of adenosine production, the inhibitor of ecto-5′-nucleotidase (AMPCP/150 mg/kg), and the specific inhibitor of adenosine degradation, the inhibitor of adenosine deaminase, EHNA (100 mg/kg) did not affect the effects over anxiety. However, AMPCP at 3 mpf, but not EHNA, reversed aggressive parameters. AMPCP also recovered the social interaction parameter at 3 mpf in animals treated in both stages, while EHNA recovered this parameter just in those animals treated with ethanol during the gastrula stage. These results suggest that long-lasting behavioural effects of ethanol can be modulated by intervention on ecto-5′-nucleotidase and adenosine deaminase activities.

Highlights

  • The behavioural impacts of prenatal exposure to ethanol include a lower IQ, learning problems, anxiety and conduct disorders

  • EHNA administration significantly reduced the mean velocity of animals treated with 1% ethanol at pharyngula at 3 mpf (P = 0.03) (Fig. 2A)

  • The inhibitors of ecto-5′-nucleotidase (AMPCP) and adenosine deaminase (EHNA) alone did not generate a significant effect on any locomotor parameter when compared to the water/ saline group (Figs. 1, 2)

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Summary

Introduction

The behavioural impacts of prenatal exposure to ethanol include a lower IQ, learning problems, anxiety and conduct disorders. AMPCP recovered the social interaction parameter at 3 mpf in animals treated in both stages, while EHNA recovered this parameter just in those animals treated with ethanol during the gastrula stage These results suggest that long-lasting behavioural effects of ethanol can be modulated by intervention on ecto-5′nucleotidase and adenosine deaminase activities. The ability of adenosine to modulate the major neurotransmitter systems related to common cognitive and behavioural consequences of early ethanol exposure brings the attention to the possible involvement of this nucleoside on these long-term effects. Because adenosine is a potent neuromodulator and ethanol is able to affect several neurotransmitters modulated by adenosine and the purinergic system itself, the objective of this research was to investigate and understand the possible effects of interventions on enzymes involved in adenosine production and degradation over the long-lasting behavioural effects caused by ethanol exposure in different stages of early development

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