4.7 Article

Translational Structural and Functional Signatures of Chronic Alcohol Effects in Mice

Journal

BIOLOGICAL PSYCHIATRY
Volume 91, Issue 12, Pages 1039-1050

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2022.02.013

Keywords

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Funding

  1. National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health [16658]
  2. Freiburg
  3. NeuroTime Erasmus1: Erasmus Mundus program of the European Commission

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This study establishes brain-wide fingerprints of alcohol effects in mice using structural and functional magnetic resonance imaging and connectome mapping. The findings show that alcohol affects both brain structure and function, and provide insights into the impact of alcohol on inflammation and different brain networks.
BACKGROUND: Alcohol acts as an addictive substance that may lead to alcohol use disorder. In humans, magnetic resonance imaging showed diverse structural and functional brain alterations associated with this complex pathology. Single magnetic resonance imaging modalities are used mostly but are insufficient to portray and understand the broad neuroadaptations to alcohol. Here, we combined structural and functional magnetic resonance imaging and connectome mapping in mice to establish brain-wide fingerprints of alcohol effects with translatable potential. METHODS: Mice underwent a chronic intermittent alcohol drinking protocol for 6 weeks before being imaged under medetomidine anesthesia. We performed open-ended multivariate analysis of structural data and functional connectivity mapping on the same subjects. RESULTS: Structural analysis showed alcohol effects for the prefrontal cortex/anterior insula, hippocampus, and somatosensory cortex. Integration with microglia histology revealed distinct alcohol signatures, suggestive of advanced (prefrontal cortex/anterior insula, somatosensory cortex) and early (hippocampus) inflammation. Functional analysis showed major alterations of insula, ventral tegmental area, and retrosplenial cortex connectivity, impacting communication patterns for salience (insula), reward (ventral tegmental area), and default mode (retrosplenial cortex) networks. The insula appeared as a most sensitive brain center across structural and functional analyses. CONCLUSIONS: This study demonstrates alcohol effects in mice, which possibly underlie lower top-down control and impaired hedonic balance documented at the behavioral level, and aligns with neuroimaging findings in humans despite the potential limitation induced by medetomidine sedation. This study paves the way to identify further biomarkers and to probe neurobiological mechanisms of alcohol effects using genetic and pharmacological manipulations in mouse models of alcohol drinking and dependence.

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