Evidence map›Paper›PMID 41778075›Full record

ArticleAddiction neuroscience2025

Concurrent consumption of ethanol and corticosterone during adolescence alters neuroimmune sensitivity in Sprague Dawley rats.

Ashley Lutzke, Ariana L Velazquez, Sarah Trapp, Andrew S Vore, Hannah E Burzynski, Maeve E Johnston, Terrence Deak

Abstract read
In one paragraph

Article in Addiction neuroscience, 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
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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

7 authors.

Ashley LutzkeDevelopmental Exposure Alcohol Research Center, Behavioral Neuroscience Program, Department of Psychology, Binghamton, NY 13902-6000, United States.ORCID 0000-0002-6496-5819
Ariana L VelazquezDevelopmental Exposure Alcohol Research Center, Behavioral Neuroscience Program, Department of Psychology, Binghamton, NY 13902-6000, United States.
Sarah TrappDevelopmental Exposure Alcohol Research Center, Behavioral Neuroscience Program, Department of Psychology, Binghamton, NY 13902-6000, United States.
Andrew S VoreDevelopmental Exposure Alcohol Research Center, Behavioral Neuroscience Program, Department of Psychology, Binghamton, NY 13902-6000, United States.
Hannah E BurzynskiDevelopmental Exposure Alcohol Research Center, Behavioral Neuroscience Program, Department of Psychology, Binghamton, NY 13902-6000, United States.
Maeve E JohnstonDevelopmental Exposure Alcohol Research Center, Behavioral Neuroscience Program, Department of Psychology, Binghamton, NY 13902-6000, United States.
Terrence DeakDevelopmental Exposure Alcohol Research Center, Behavioral Neuroscience Program, Department of Psychology, Binghamton, NY 13902-6000, United States.

Funding

Social Anxiety, Stress and Ethanol Sensitivity in Adolescence and AdulthoodP50AA017823 · NIAAA · UPSTATE MEDICAL UNIVERSITY · PI J. DAVID JENTSCH · 2009 to 2026
$30.5M
Development and Neuroadaptations in Alcohol and Addictions (DNA2)T32AA025606 · NIAAA · STATE UNIVERSITY OF NY,BINGHAMTON · PI J. DAVID JENTSCH · 2017 to 2026
$2.7M
CNS-mediated fever after Adolescent Intermittent EthanolR01AA030469 · NIAAA · STATE UNIVERSITY OF NY,BINGHAMTON · PI Terrence Deak · 2023 to 2026
$1.7M
NIAAA NIH HHS P50 AA017823NIAAA NIH HHS R01 AA030469NIAAA NIH HHS T32 AA025606
6 · The paper itself

Abstract

Chronic stress and alcohol consumption influence various features of neuroimmune reactivity, including neurobehavioral outcomes, induction of neuroimmune genes, blood-brain barrier (BBB) permeability, and core body temperature regulation. The goal of the present studies was to characterize a novel model of chronic ethanol intake in which exogenous corticosterone (CORT), a principal end-product of the Hypothalamic-Pituitary-Adrenal (HPA) axis, was co-consumed in 10 % ethanol. In adolescence (P28-32), pair-housed Sprague-Dawley rats were given a single bottle containing 10 % ethanol with varying concentrations of CORT (0, 25, 50, or 100μg/mL) for 48 h, followed by 48 h of tap water. This four-day sequence was repeated for 12 cycles, ending in early adulthood (P76-80). In Experiment 1, following CORT and ethanol exposure, rats were challenged with restraint stress (30 min), and changes in neuroimmune gene expression were evaluated. Rats with a history of 10 % ethanol + 100μg/mL CORT showed increased interleukin (IL)-6 mRNA expression in the hippocampus relative to water comparators. Experiment 2 probed BBB permeability after perfusion with FITC-labeled dextran (20 kDa), and no changes were found. Remaining experiments evaluated the effects of ethanol/CORT drinking on ethanol-induced hypothermia (Experiment 3) and polyinosinic:polycytidylic acid (Poly I:C)-induced fever (Experiment 4). In females, ethanol consumption (regardless of CORT) delayed return to baseline following the hypothermic response, and in males, 25μg/mL CORT exclusively suppressed fever following Poly I:C challenge. Together, these findings validate a concurrent exposure model of intermittent CORT and ethanol which is translationally relevant to the adolescent experience, and uncovered ethanol- and CORT-induced changes in adult neuroimmune reactivity.

Indexed as

Adolescent ethanol exposureBBB permeabilityCorticosterone consumptionEthanol-induced hypothermiaNeuroimmunePoly I:C fever

Identifiers

PMID41778075
PMCPMC12952763

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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.