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Chronic Intermittent Ethanol Vapor Exposure Paired with Two-Bottle Choice to Model Alcohol Use Disorder
Published on: June 23, 2023
Alcohol dependence and free-choice drinking in mice
1Charleston Alcohol Research Center, Department of Psychiatry and Behavioral Sciences, Medical University of South Carolina, 67 President St., RM 471, MSC 861, Charleston, SC 29425, USA.
Chronic intermittent ethanol (CIE) exposure in mice leads to increased alcohol drinking, mimicking human alcoholism. This model reveals neuroadaptations in brain signaling, offering insights for developing effective alcohol dependence treatments.
Area of Science:
- Neuroscience
- Pharmacology
- Addiction Research
Background:
- Alcohol dependence is a significant global health issue.
- Animal models are essential for understanding the neurobiology of alcoholism.
- A key feature of alcoholism is escalating alcohol consumption over time.
Purpose of the Study:
- To describe the chronic intermittent ethanol (CIE) exposure and free-choice drinking model in mice.
- To highlight the utility of this model for studying the mechanisms of excessive alcohol consumption.
- To discuss the translational potential of findings from this model to human alcoholism.
Main Methods:
- Mice undergo chronic intermittent ethanol (CIE) exposure to induce dependence.
- Voluntary ethanol drinking is assessed using a limited access procedure (2-hour access).
- Neuroadaptations in glutamatergic and corticotropin-releasing factor signaling are investigated.
Main Results:
- Dependent mice exhibit significantly increased voluntary ethanol intake compared to non-dependent controls.
- Elevated blood and brain ethanol concentrations are observed in dependent mice.
- Neuroadaptations in specific brain signaling pathways are linked to increased drinking behavior.
Conclusions:
- The CIE and free-choice drinking model effectively replicates key features of human alcohol dependence.
- This model provides valuable insights into the neurobiological mechanisms underlying excessive alcohol consumption.
- Findings from this model have translational potential for developing novel therapeutic strategies for alcohol dependence.
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