Evidence map›Paper›PMID 41332614›Full record

ArticlebioRxiv : the preprint server for biology2025

Impact of chronic alcohol and stress on mid-life cognition and locus coeruleus integrity.

O Revka, S J Belculfine, L Fitts, K E Nippert, Caf Teves, P M Reis, S Tenney, B E Packer, I Garcia Alvarez, O Milstein and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

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.

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

5 · Who and what money

Authors and funding

13 authors.

O RevkaDepartment of Biology, University of Massachusetts Amherst.
S J BelculfineDepartment of Biology, University of Massachusetts Amherst.
L FittsDepartment of Biology, University of Massachusetts Amherst.
K E NippertDepartment of Biology, University of Massachusetts Amherst.
Caf TevesDepartment of Biology, University of Massachusetts Amherst.
P M ReisDepartment of Biology, University of Massachusetts Amherst.
S TenneyDepartment of Biology, University of Massachusetts Amherst.
B E PackerDepartment of Biology, University of Massachusetts Amherst.
I Garcia AlvarezDepartment of Psychological and Brain Sciences, University of Massachusetts Amherst.
O MilsteinDepartment of Biology, University of Massachusetts Amherst.
M Coutinho da SilvaDepartment of Biology, University of Massachusetts Amherst.
D E MoormanDepartment of Psychological and Brain Sciences, University of Massachusetts Amherst.ORCID 0000-0002-5755-0789
E M VazeyDepartment of Biology, University of Massachusetts Amherst.ORCID 0000-0003-3311-9414

Funding

4/8: INIA Stress and Chronic Alcohol Interactions: Impact of stress mediated locus coeruleus dysregulation on cognitive control and excessive drinkingU01AA025481 · NIAAA · UNIVERSITY OF MASSACHUSETTS AMHERST · PI DAVID E MOORMAN, Elena Vazey · 2017 to 2026
$4.2M
NIAAA NIH HHS U01 AA025481
6 · The paper itself

Abstract

Background: Excessive alcohol consumption and stress are associated with structural and functional alterations in the brain and impaired cognition. However, the persistence of long-term neural impacts after alcohol and stress are less understood. This study investigated midlife cognition and neuropathological changes following a history of alcohol and stress exposure. Methods: C57BL/6J mice acclimated to ethanol drinking (15% v/v) before exposure to four cycles of alternating chronic intermittent ethanol (CIE) vapor exposure and repeated forced swim stress (FSS), with control groups exposed to air and no stress (AIR/NS). After three months of abstinence, mice were evaluated at midlife (11 months old) on volitional drinking and a final CIE/FSS challenge for stress induced drinking. Spatial learning and cognitive flexibility were assessed using the Barnes maze before brains were collected to evaluate locus coeruleus integrity at 12 months old. Results: CIE/FSS increased volitional alcohol intake, and this drinking phenotype persisted through to midlife despite extended abstinence. CIE/FSS mice showed intact spatial learning but impaired flexibility in the Barnes maze reversal phase. Flexibility impairments were driven by decreased time in the target quadrant and increased errors during the reversal test compared to AIR/NS. Furthermore, CIE/FSS mice showed pathological measures of reduced locus coeruleus integrity common to dementia related disorders, including elevated markers of oxidative stress, apoptosis and reduced autoinhibitory function. Conclusions: Our findings highlight the long-lasting impact of alcohol and stress exposure on cognition, with flexibility impairments persisting into midlife. In addition to cognitive changes, alcohol and stress history produced pathological changes in the locus coeruleus, an area known to mediate cognitive flexibility via its forebrain projections. Together, these results give an insight into the long-lasting impacts of chronic alcohol and stress and how they may accelerate age-related cognitive decline.

Indexed as

agingalcohol use disorder (AUD)cognitive flexibilitydementiareversal learning

Identifiers

PMID41332614
PMCPMC12667861

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.