Evidence map›Paper›PMID 41679356›Full record

ArticleAlcohol (Fayetteville, N.Y.)2026

CeA-projecting VTA neurons contribute to alcohol withdrawal-induced anxiety-like behavior in male and female rats.

Scott B Klinefelter, Loren Johnson, Shealan C Cruise, Sydney Vita, Candace Weeden, Maria E Secci, Nicholas W Gilpin, Elizabeth M Avegno

Abstract read
In one paragraph

Article in Alcohol (Fayetteville, N.Y.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Scott B KlinefelterDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Loren JohnsonDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Shealan C CruiseDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Sydney VitaDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Candace WeedenDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Maria E SecciDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Nicholas W GilpinDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA; Alcohol and Drug Abuse Center of Excellence, Louisiana State University Health Sciences Center School of Medicine, New Orleans, LA, 70112, USA; Veterans Affairs Southeast Louisiana Healthcare System, New Orleans, LA, 70112, USA.
Elizabeth M AvegnoDepartment of Physiology, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA; Alcohol and Drug Abuse Center of Excellence, Louisiana State University Health Sciences Center School of Medicine, New Orleans, LA, 70112, USA. Electronic address: eavegn@lsuhsc.edu.

Funding

Orexin modulation of brain reward-brain stress system interactions in alcohol withdrawal anxietyK01AA028541 · NIAAA · LSU HEALTH SCIENCES CENTER · PI Elizabeth Minor Avegno · 2022 to 2026
$818k
NIAAA NIH HHS K01 AA028541
6 · The paper itself

Abstract

Alcohol use disorder often causes patients to experience negative affect during withdrawal, and anxiety is positively correlated with relapse during abstinence. The neural adaptations that occur during the transition to dependence are not entirely understood, but they may include interactions between mesolimbic reward circuits and brain stress circuits. Previously, we demonstrated that chronic alcohol exposure leads to activation of ventral tegmental area (VTA) neurons projecting to the central amygdala (CeA) during acute withdrawal, raising the possibility that these cells may underlie some behavioral changes observed during alcohol withdrawal. Here, we investigated the role of VTA-CeA circuitry in anxiety-like behavior during acute alcohol withdrawal in rats. Using a dual virus approach to transfect CeA-projecting VTA neurons with excitatory or inhibitory DREADDs, we demonstrate that VTA-CeA circuit activation increases anxiety-like behavior in otherwise experimentally naïve adult male and female Wistar rats, and that VTA-CeA circuit inhibition rescues increased anxiety-like behavior during acute withdrawal from chronic alcohol exposure. Collectively, the results of these experiments suggest that VTA-CeA circuitry may contribute to anxiety-like behavior and may serve as a target for alleviating alcohol withdrawal-induced anxiety.

Indexed as

AnxietyCentral Amygdaloid NucleusEthanolNeuronsSubstance Withdrawal SyndromeVentral Tegmental AreaAnimalsFemaleMaleRatsRats, WistarEthanolAlcoholAnxietyCentral amygdalaRatsVentral tegmental areaWithdrawal

Identifiers

PMID41679356
PMCPMC13353520

What Socratic holds

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Registered trials

None linked

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.