Original Article
Similar Ethanol Drinking in Adolescent and Adult C57BL/6J Mice After Chronic Ethanol Exposure and Withdrawal
Article first published online: 8 JAN 2013
DOI: 10.1111/acer.12056
Copyright © 2013 by the Research Society on Alcoholism
Issue

Alcoholism: Clinical and Experimental Research
Early View (Online Version of Record published before inclusion in an issue)
Additional Information
How to Cite
Carrara-Nascimento, P. F., Lopez, M. F., Becker, H. C., Olive, M. F. and Camarini, R. (2013), Similar Ethanol Drinking in Adolescent and Adult C57BL/6J Mice After Chronic Ethanol Exposure and Withdrawal. Alcoholism: Clinical and Experimental Research. doi: 10.1111/acer.12056
Publication History
- Article first published online: 8 JAN 2013
- Manuscript Accepted: 11 OCT 2012
- Manuscript Received: 15 MAY 2012
Funded by
- Fundação de Amparo à Pesquisa do Estado de São Paulo. Grant Numbers: AA013852, AA014095
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
- Conselho Nacional de Desenvolvimento Científico e Tecnológico
- Abstract
- Article
- References
- Cited By
Keywords:
- Ethanol Drinking;
- Chronic Ethanol Exposure;
- Adolescent;
- Withdrawal;
- C57BL/6J mice
Background
Increasing evidence shows that excessive alcohol consumption during adolescence increases vulnerability to alcohol use disorders in adulthood. The aim of this study was to examine differences between adolescent and adult C57BL/6J mice in drinking behavior and blood ethanol (EtOH) concentrations (BECs) after chronic EtOH exposure and withdrawal.
Methods
Male adolescent (PND = 28 to 30) and adult (PND = 70) C57BL/6J mice were allowed to consume EtOH in a 2-bottle choice paradigm (15% EtOH vs. water) for 3 weeks (Baseline drinking, Test 1, and Test 2), which were interspersed with 2 cycles (Cycles I and II) of chronic EtOH vapor or air inhalation (16 hours) and withdrawal (8 hours). BECs were determined during both cycles.
Results
Chronic EtOH exposure led to increased EtOH intake during Test 1 and Test 2 in both adolescent and adult mice compared with air-exposed controls, and no differences between age groups were observed. During Cycle I adult mice showed higher BECs compared with adolescents. During Cycle II, BECs were lower in adult mice as compared to Cycle I, and BECs in adolescent mice did not change between the 2 cycles.
Conclusions
Chronic EtOH exposure followed by withdrawal periods increases EtOH consumption similarly in both adolescent and adult mice, despite differences in BECs.

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