| Literature DB >> 31421226 |
Maria Cecilia Manenti Alexandre1, Niuany Viel Mendes2, Carolina Antunes Torres2, Samira Leila Baldin2, Henrique Teza Bernardo2, Rahisa Scussel3, Suelen Baggio4, Ben Hur Marins Mussulini5, Kamila Cagliari Zenki4, Maria Inês da Rosa6, Eduardo Pacheco Rico7.
Abstract
Binge drinking is defined as the infrequent consumption of excessive doses of alcohol in a short period of time. Zebrafish is a reliable model to investigate ethanol consumption impact on the CNS, including reward signaling like dopaminergic neurotransmission system. The aim of this study was to evaluate zebrafish brain dopaminergic parameters after intermittent weekly ethanol exposure (WEE), which mimics binge drinking. Thus, adult zebrafish were exposed to ethanol (1.4% v/v) for 30 min, once a week for three consecutive weeks. The groups were divided according to different time points after the third exposure and name as follow: immediately (WEEI), two days (WEE-2), and nine days (WEE-9) after last exposure to ethanol. Brain dopaminergic function was assessed by the activity of the dopamine transporters (DAT); monoamine oxidase (MAO) activity; dopamine and noradrenaline levels by chromatography. The WEE-I and WEE-2 groups presented a significant increase in DAT activity. The MAO activity was decreased for WEE-2 and WEE-9 groups. The WEE-2 and WEE-9 groups presented an increase in brain dopamine levels, while noradrenaline levels were not affected. Therefore, dopaminergic parameters are still altered two and nine days after the last ethanol exposure in this binge experimental model, resulting in a modulatory event in this neurotransmission pathway.Entities:
Keywords: Brain; Catecholamine; Dopamine transporter; Monoamine oxidase; Weekly ethanol exposure; Zebrafish
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Year: 2019 PMID: 31421226 DOI: 10.1016/j.ntt.2019.106822
Source DB: PubMed Journal: Neurotoxicol Teratol ISSN: 0892-0362 Impact factor: 3.763