Document Detail


Chronobiology of alcohol: studies in C57BL/6J and DBA/2J inbred mice.
MedLine Citation:
PMID:  23313401     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Human alcoholics display dramatic disruptions of circadian rhythms that may contribute to the maintenance of excessive drinking, thus creating a vicious cycle. While clinical studies cannot establish direct causal mechanisms, recent animal experiments have revealed bidirectional interactions between circadian rhythms and ethanol intake, suggesting that the chronobiological disruptions seen in human alcoholics are mediated in part by alterations in circadian pacemaker function. The present study was designed to further explore these interactions using C57BL/6J (B6) and DBA/2J (D2) inbred mice, two widely employed strains differing in both circadian and alcohol-related phenotypes. Mice were maintained in running-wheel cages with or without free-choice access to ethanol and exposed to a variety of lighting regimens, including standard light-dark cycles, constant darkness, constant light, and a "shift-lag" schedule consisting of repeated light-dark phase shifts. Relative to the standard light-dark cycle, B6 mice showed reduced ethanol intake in both constant darkness and constant light, while D2 mice showed reduced ethanol intake only in constant darkness. In contrast, shift-lag lighting failed to affect ethanol intake in either strain. Access to ethanol altered daily activity patterns in both B6 and D2 mice, and increased activity levels in D2 mice, but had no effects on other circadian parameters. Thus, the overall pattern of results was broadly similar in both strains, and consistent with previous observations that chronic ethanol intake alters circadian activity patterns while environmental perturbation of circadian rhythms modulates voluntary ethanol intake. These results suggest that circadian-based interventions may prove useful in the management of alcohol use disorders.
Authors:
Alan M Rosenwasser; Michael C Fixaris
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, N.I.H., Extramural     Date:  2013-01-10
Journal Detail:
Title:  Physiology & behavior     Volume:  110-111     ISSN:  1873-507X     ISO Abbreviation:  Physiol. Behav.     Publication Date:  2013 Feb 
Date Detail:
Created Date:  2013-04-01     Completed Date:  2013-09-24     Revised Date:  2014-02-20    
Medline Journal Info:
Nlm Unique ID:  0151504     Medline TA:  Physiol Behav     Country:  United States    
Other Details:
Languages:  eng     Pagination:  140-7     Citation Subset:  IM    
Copyright Information:
Copyright © 2013 Elsevier Inc. All rights reserved.
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MeSH Terms
Descriptor/Qualifier:
Alcohol Drinking / psychology*
Animals
Central Nervous System Depressants / pharmacology
Chronobiology Phenomena / physiology*
Circadian Rhythm / physiology*
Drinking
Ethanol / pharmacology
Lighting
Male
Mice
Mice, Inbred C57BL
Mice, Inbred DBA
Motor Activity / physiology
Photoperiod
Species Specificity
Grant Support
ID/Acronym/Agency:
R21 AA013893/AA/NIAAA NIH HHS; U01 AA13641/AA/NIAAA NIH HHS
Chemical
Reg. No./Substance:
0/Central Nervous System Depressants; 3K9958V90M/Ethanol
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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