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Updated: May 23, 2026

Murine Drinking Models in the Development of Pharmacotherapies for Alcoholism: Drinking in the Dark and Two-bottle Choice
Published on: January 7, 2019
Ivermectin reduces alcohol intake and preference in mice
Megan M Yardley1, Letisha Wyatt, Sheraz Khoja
1Department of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, 1985 Zonal Avenue, Los Angeles, CA 90033, USA.
Ivermectin (IVM) significantly reduced alcohol consumption in mice across multiple models. This suggests IVM may be a promising therapeutic strategy for alcohol use disorders (AUDs).
Area of Science:
- Neuroscience
- Pharmacology
- Addiction Research
Background:
- High rates of therapeutic failure in alcohol use disorder (AUD) management necessitate novel interventions.
- Ivermectin (IVM), an antiparasitic drug, was previously found to antagonize ethanol's effects on P2X4 receptors.
- This interaction suggested a potential role for IVM in reducing alcohol consumption.
Purpose of the Study:
- To investigate the efficacy of ivermectin (IVM) in reducing alcohol intake.
- To evaluate IVM's effects across various alcohol self-administration models in mice.
- To determine the dose-dependency and temporal profile of IVM's effects on alcohol consumption.
Main Methods:
- Male and female C57BL/6 mice were used in several alcohol self-administration paradigms.
- Ivermectin (1.25-10 mg/kg, intraperitoneal) was administered.
- Alcohol consumption, binge drinking, and operant self-administration of alcohol and sucrose were measured.
Main Results:
- Ivermectin significantly reduced 24-h alcohol consumption and binge drinking.
- Operant alcohol self-administration was dose-dependently reduced by IVM.
- IVM also reduced saccharin consumption but not sucrose self-administration, indicating some specificity.
Conclusions:
- Ivermectin effectively reduces alcohol intake in multiple preclinical models of alcohol consumption.
- The findings support the potential of ivermectin as a novel therapeutic agent for alcohol use disorders.
- Further research into IVM's mechanisms and clinical efficacy for AUDs is warranted.
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