Alcohol abstinence precipitates alcohol seeking and aversion-resistant intake in association with increased BNST activity.
Marie A Doyle, Hye Jean Yoon, Megan E Altemus, Anika S Park, Martha E Troutman, Laura Grunenkovaite, Danielle N Adank, Caitlyn M Edwards, Nia A Chetkovich, Sabrina D Hallal and 4 more
Article in Molecular psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
2 · The registry
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Marcela Brissova · 2012 to 2026
$29.3M
VAREC Research CoreP60AA031124 · NIAAA · VANDERBILT UNIVERSITY · PI Danny G. Winder · 2024 to 2026
$7.1M
Alcohol action on extended amygdala glutamate synapsesR37AA019455 · NIAAA · VANDERBILT UNIVERSITY · PI WINDER, DANNY G. · 2015 to 2024
$3.9M
Circuit control of motivation to take and seek alcoholR01AA030931 · NIAAA · VANDERBILT UNIVERSITY · PI Erin Calipari · 2023 to 2026
$2.3M
Mesocortical neuromodulation in punishment-resistant alcohol drinkingR01AA030115 · NIAAA · VANDERBILT UNIVERSITY · PI Cody Siciliano · 2022 to 2026
$2.1M
8/8: INIA Stress and Chronic Alcohol Interactions: Cross-species plasticity signatures of alcohol and stressU01AA029971 · NIAAA · VANDERBILT UNIVERSITY · PI Cody Siciliano · 2022 to 2026
$2.0M
Alcohol action on extended amygdala glutamate synapsesR01AA019455 · NIAAA · VANDERBILT UNIVERSITY · PI WINDER, DANNY G. · 2010 to 2014
$1.8M
Defining the role of cortical circuit dynamics in learning and addictionR00DA045103 · NIDA · VANDERBILT UNIVERSITY · PI SICILIANO, CODY · 2020 to 2022
$764k
Defining the role of cortical circuit dynamics in learning and addictionK99DA045103 · NIDA · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SICILIANO, CODY · 2018 to 2019
$366k
The role of BNST PKCdelta neurons in compulsive ethanol intakeK99AA031509 · NIAAA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Marie Althea Doyle · 2025 to 2026
$313k
Defining the cell-type specific control of alcohol drinkingF31AA030916 · NIAAA · VANDERBILT UNIVERSITY · PI Hye Jean Yoon · 2023 to 2026
$152k
Investigating the role of BNST GluN2D subunit-containing NMDARs in ethanol-induced plasticity and behaviorF32AA029592 · NIAAA · VANDERBILT UNIVERSITY · PI DOYLE, MARIE ALTHEA · 2021 to 2022
$133k
NIAAA NIH HHS F31 AA030901NIAAA NIH HHS F31 AA030916NIAAA NIH HHS F32 AA029592NIAAA NIH HHS F32 AA031404NIAAA NIH HHS K99 AA031509NIAAA NIH HHS P60 AA031124NIAAA NIH HHS R01 AA019455NIAAA NIH HHS R01 AA030115NIAAA NIH HHS R01 AA030931NIAAA NIH HHS R37 AA019455NIAAA NIH HHS U01 AA029971NIDA NIH HHS K99 DA045103NIDA NIH HHS R00 DA045103NIDDK NIH HHS P30 DK020593U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) DK020593U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) DK135073U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA019455U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA029592U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA029971U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA030115U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA030901U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA030916U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA030931U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA031124U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA031404U.S. Department of Health & Human Services | NIH | National Institute on Alcohol Abuse and Alcoholism (NIAAA) AA031509U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) DA045103
6 · The paper itself
Abstract
Alcohol Use Disorder (AUD) is defined by a common diagnostic framework, yet individuals show diverse drinking patterns and relapse vulnerabilities during abstinence, reflecting neurobiological heterogeneity. The bed nucleus of the stria terminalis (BNST) is well positioned to contribute to this variability. To understand how BNST activity co-segregates with individual alcohol behavior trajectories, we used the Structured Tracking of Alcohol Reinforcement (STAR) operant task to phenotype C57BL/6J mice as high, low, or aversion-resistant ethanol drinkers. During initial self-administration, dBNST cFos+ counts correlated with intake, linking dBNST activation to operant drinking. Using in vivo fiber photometry, we found that aversion-resistant drinkers displayed elevated dBNST calcium transients during drinking bouts despite similar intake across groups, consistent with heightened dBNST recruitment. Forced abstinence uncovered prominent phenotype-specific adaptations, where ethanol seeking during protracted, but not early, abstinence predicted aversion-resistant intake. High and low drinkers reduced seeking behavior across abstinence, whereas aversion-resistant drinkers persisted. Consistently, dBNST calcium transients increased during protracted abstinence seeking only in aversion-resistant drinkers, highlighting phenotype-specific plasticity. Comparing mice exposed to abstinence versus only operant training showed that abstinence itself potentiates aversion-resistant intake. Finally, these dBNST dynamics were ethanol-specific, as saccharin drinking more closely reflected activity for high drinkers. Together, these findings reveal that ethanol abstinence precipitates ethanol seeking and aversion-resistant intake, associated with phenotypic dBNST calcium dynamics. Because causality was not established, future studies are needed to define mechanistic contributions of dBNST activity to phenotypic behaviors. By uncovering how dBNST activity adapts in aversion-resistant drinkers, this work offers insight into AUD heterogeneity.
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.
Alcohol abstinence precipitates alcohol seeking and aversion-resistant intake in association with increased BNST activity. · full record | Socratic