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Alcohol Dependence Modifies Brain Networks Activated During Withdrawal and Reaccess: A c-Fos–Based Analysis in Mice

  • Author Footnotes
    1 AVR and CAOC contributed equally to this work.
    Alison V. Roland
    Footnotes
    1 AVR and CAOC contributed equally to this work.
    Affiliations
    Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, North Carolina
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  • Author Footnotes
    1 AVR and CAOC contributed equally to this work.
    Cesar A.O. Coelho
    Footnotes
    1 AVR and CAOC contributed equally to this work.
    Affiliations
    Neuroscience and Mental Health, The Hospital for Sick Children, Toronto, Ontario, Canada
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  • Harold L. Haun
    Affiliations
    Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, North Carolina
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  • Carol A. Gianessi
    Affiliations
    Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, North Carolina
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  • Marcelo F. Lopez
    Affiliations
    Charleston Alcohol Research Center, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina

    Charleston Alcohol Research Center, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina
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  • Shannon D’Ambrosio
    Affiliations
    Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, North Carolina
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  • Samantha N. Machinski
    Affiliations
    Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, North Carolina
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  • Christopher D. Kroenke
    Affiliations
    Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon

    Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, Oregon

    Advanced Imaging Research Center, Oregon Health & Science University, Portland, Oregon
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  • Paul W. Frankland
    Affiliations
    Neuroscience and Mental Health, The Hospital for Sick Children, Toronto, Ontario, Canada

    Department of Physiology, University of Toronto, Toronto, Ontario, Canada

    Department of Psychology, University of Toronto, Toronto, Ontario, Canada

    Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada
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  • Howard C. Becker
    Affiliations
    Charleston Alcohol Research Center, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina

    Charleston Alcohol Research Center, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, Charleston, South Carolina

    Department of Neuroscience, Medical University of South Carolina, Charleston, South Carolina

    Ralph H. Johnson Department of Veterans Affairs Medical Center, Charleston, South Carolina
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  • Thomas L. Kash
    Correspondence
    Address correspondence to Thomas L. Kash, Ph.D.
    Affiliations
    Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, North Carolina

    Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill, North Carolina
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  • Author Footnotes
    1 AVR and CAOC contributed equally to this work.

      Abstract

      Background

      High-level alcohol consumption causes neuroplastic changes in the brain that promote pathological drinking behavior. Some of these changes have been characterized in defined brain circuits and cell types, but unbiased approaches are needed to explore broader patterns of adaptations.

      Methods

      We used whole-brain c-Fos mapping and network analysis to assess patterns of neuronal activity during alcohol withdrawal and following reaccess in a well-characterized model of alcohol dependence. Mice underwent 4 cycles of chronic intermittent ethanol to increase voluntary alcohol consumption, and a subset underwent forced swim stress to further escalate consumption. Brains were collected either 24 hours (withdrawal) or immediately following a 1-hour period of alcohol reaccess. c-fos counts were obtained for 110 brain regions using iDISCO and ClearMap. Then, we classified mice as high or low drinkers and used graph theory to identify changes in network properties associated with high-drinking behavior.

      Results

      During withdrawal, chronic intermittent ethanol mice displayed widespread increased c-Fos expression relative to air-exposed mice, independent of forced swim stress. Reaccess drinking reversed this increase. Network modularity, a measure of segregation into communities, was increased in high-drinking mice after alcohol reaccess relative to withdrawal. The cortical amygdala showed increased cross-community coactivation during withdrawal in high-drinking mice, and cortical amygdala silencing in chronic intermittent ethanol mice reduced voluntary drinking.

      Conclusions

      Alcohol withdrawal in dependent mice causes changes in brain network organization that are attenuated by reaccess drinking. Olfactory brain regions, including the cortical amygdala, drive some of these changes and may play an important but underappreciated role in alcohol dependence.

      Keywords

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