Evidence map›Paper›PMID 41262411›Full record

ArticleBrain communications2025

The effect of chronic stress and chronic alcohol intake on behaviour, brain volume, and functional connectivity in a longitudinal rat model.

Jalil Rasgado-Toledo, Diego Angeles-Valdez, César J Carranza-Aguilar, Alejandra Lopez-Castro, Luis A Trujillo-Villarreal, David Medina-Sánchez, Mariana S Serrano-Ramirez, A Débora Elizarrarás-Herrera, Sarael Alcauter, Ilse Delint-Ramirez and 4 more

Abstract read
In one paragraph

Article in Brain communications, 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

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

14 authors.

Jalil Rasgado-ToledoInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.ORCID https://orcid.org/0000-0001-5216-7177
Diego Angeles-ValdezInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.ORCID https://orcid.org/0000-0001-8029-8369
César J Carranza-AguilarInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.
Alejandra Lopez-CastroInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.
Luis A Trujillo-VillarrealInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.
David Medina-SánchezInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.
Mariana S Serrano-RamirezInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.
A Débora Elizarrarás-HerreraInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.
Sarael AlcauterInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.
Ilse Delint-RamirezDepartments of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Ranier GutierrezDepartment of Pharmacology, Laboratory of Neurobiology of Appetite, Center for Research and Advanced Studies of the National Polytechnic Institute, Mexico City 07360, Mexico.
Gabriel A DevenyiDepartment of Psychiatry, McGill University, Montreal, QC, Canada H3A 1A1.ORCID https://orcid.org/0000-0002-7766-1187
M Mallar ChakravartyDepartment of Psychiatry, McGill University, Montreal, QC, Canada H3A 1A1.
Eduardo A Garza-VillarrealInstitute of Neurobiology, Universidad Nacional Autónoma de México campus Juriquilla, Santiago de Querétaro, Querétaro 76230, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathological chronic stress is stress exceeding the organism's ability to cope physiologically, which may act as a risk factor in the onset and relapse of alcohol use disorder. Chronic-restraint stress (CRS) and ethanol intake are independently known to induce changes in brain structure and function, however, their combined effects on neurodevelopment over long periods of time remains largely unexplored. We conducted an in vivo longitudinal rat model with three main goals. 1) to determine if chronic stress increases ethanol intake; 2) to determine the effect of chronic- stress and ethanol intake in behavioural measures, brain structure, and function; and 3) to investigate the effect of sex. This observational study included Wistar rats assigned to four groups: 1) ethanol consumption (EtOH+/CRS-), 2) stress exposure (EtOH-/CRS+), 3) both ethanol and stress exposure (EtOH+/CRS+), and 4) control group (EtOH-/CRS-). Our results showed that chronic stress did not affect ethanol intake but led to reduced body weight gain, elevated corticosterone levels, and impaired recognition memory. Structural MRI revealed that both exposures produced additive brain volume changes in olfactory bulb, orbitofrontal cortex, caudate-putamen, hippocampus, and cerebellum. Functional connectivity analysis using network-based statistics identified disrupted cortical-subcortical connections. Results found here were sex-dependent in terms of volumetric changes (higher effects on males) and functional connectivity (higher effects on females). Findings suggest sex-dependent mechanisms where both chronic- ethanol intake and stress affect brain plasticity during neurodevelopment. Understanding region-specific vulnerabilities is crucial for addressing alcohol use disorders and stress-related neuropathology.

Indexed as

alcohol use disorder (AUD)animal modelschronic restraint stress (CRS)IA2BClongitudinal MRI

Identifiers

PMID41262411
PMCPMC12624392

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Registered trials

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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 OpenQuestion graph.