Translational evidence for increased central amygdala IL-6 activity in alcohol dependence

Alcohol use disorder (AUD) is one of the most prevalent mental health disorders worldwide yet effective therapeutics remain limited. Mounting evidence indicates that dysregulated immune signaling in the brain plays a role in AUD pathophysiology. Activation of pro-inflammatory pathways like the interleukin-6 (IL-6) pathway represents a potential point of convergence between synaptic dysfunction and motivational changes in AUD that remain undiscovered. Thus, using a translational neuroscience approach and well-established model of chronic alcohol intake, we investigated the cell-type specific role of IL-6 signaling in the central amygdala, a critical region in the development and maintenance of alcohol dependence. We demonstrate that chronic alcohol exposure recruits IL-6-related pathways in humans and rodents via astrocytic, neuronal, and microglial mechanisms, and that IL-6 inhibits central amygdala GABAergic transmission. Notably, systemic administration of an IL-6 receptor antibody decreased alcohol drinking in alcohol-dependent female mice. Collectively, our findings support IL-6 inhibition as a novel-neuroimmune-targeted therapeutic strategy to reduce excessive drinking in the context of AUD.

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Publication Details

Journal
Journal of Neuroinflammation
Published
2026-05-22
DOI
https://doi.org/10.1186/s12974-026-03868-2
Primary Topic
Neurotransmitter Receptor Influence on Behavior
Type
article
Field-Weighted Citation Impact
0.00

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article

Translational evidence for increased central amygdala IL-6 activity in alcohol dependence

Sophia Khom, Roman Vlkolinský, Marina Guizzetti, Jessica A. Cucinello‐Ragland et al.
Journal of Neuroinflammation
Neurotransmitter Receptor Influence on Behavior
article

Translational evidence for increased central amygdala IL-6 activity in alcohol dependence

Sophia Khom, Roman Vlkolinský, Marina Guizzetti, Jessica A. Cucinello‐Ragland, Larry Rodriguez, Taylor Fitzpatrick‐Schmidt, Nihal A. Salem, Michal Bajo, Joel G. Hashimoto, Michela Palmisano, Celsey M. St. Onge, Bryan Cruz, Vittoria Borgonetti, Amanda J. Roberts, Tali Nadav, R Dayne Mayfield, Scott Edwards, Chloe Erikson, Christopher S. Oleata, Marisa Roberto
article en

Abstract

Alcohol use disorder (AUD) is one of the most prevalent mental health disorders worldwide yet effective therapeutics remain limited. Mounting evidence indicates that dysregulated immune signaling in the brain plays a role in AUD pathophysiology. Activation of pro-inflammatory pathways like the interleukin-6 (IL-6) pathway represents a potential point of convergence between synaptic dysfunction and motivational changes in AUD that remain undiscovered. Thus, using a translational neuroscience approach and well-established model of chronic alcohol intake, we investigated the cell-type specific role of IL-6 signaling in the central amygdala, a critical region in the development and maintenance of alcohol dependence. We demonstrate that chronic alcohol exposure recruits IL-6-related pathways in humans and rodents via astrocytic, neuronal, and microglial mechanisms, and that IL-6 inhibits central amygdala GABAergic transmission. Notably, systemic administration of an IL-6 receptor antibody decreased alcohol drinking in alcohol-dependent female mice. Collectively, our findings support IL-6 inhibition as a novel-neuroimmune-targeted therapeutic strategy to reduce excessive drinking in the context of AUD.

Journal of Neuroinflammation
University of Siena (IT), Scripps Research Institute (US), University of Vienna (AT), University of Tennessee Health Science Center (US), Oregon Health & Science University (US), VA Portland Health Care System (US), Louisiana State University Health Sciences Center New Orleans (US), The University of Texas at Austin (US)
U.S. Department of Veterans Affairs, National Institute on Alcohol Abuse and Alcoholism, National Institute on Drug Abuse
Good health and well-being
Openalex Percentile: Top 7%
Neurotransmitter Receptor Influence on Behavior
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