Evidence map›Paper›PMID 37573960›Full record

ArticlePhysiology & behavior2023

Sex differences in ethanol consumption and drinking despite negative consequences following adolescent social isolation stress in male and female rats.

Bryan D McElroy, Chen Li, Nicholas S McCloskey, Lynn G Kirby

Abstract read
In one paragraph

Article in Physiology & behavior, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  7. Role of serotonin neurons in the dorsal raphe nucleus in heroin self-administration and punishment.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
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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

4 authors.

Bryan D McElroyCenter for Substance Abuse Research, Lewis Katz School of Medicine at Temple University Philadelphia, PA, 19140, United States of America. Electronic address: bryan.mcelroy@temple.edu.
Chen LiCenter for Substance Abuse Research, Lewis Katz School of Medicine at Temple University Philadelphia, PA, 19140, United States of America.
Nicholas S McCloskeyCenter for Substance Abuse Research, Lewis Katz School of Medicine at Temple University Philadelphia, PA, 19140, United States of America.
Lynn G KirbyCenter for Substance Abuse Research, Lewis Katz School of Medicine at Temple University Philadelphia, PA, 19140, United States of America.

Funding

Pilot Projects Core (PPC)P30DA013429 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI Munir Gunes Kutlu · 2000 to 2026
$34.6M
TRAINING PROGRAM: DRUGS OF ABUSE RELATED NEUROPEPTIDEST32DA007237 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI ELLEN M UNTERWALD · 1988 to 2026
$10.6M
Regulation of 5-HT circuits by CRF and GABA in opioid addiction and stress-induced relapseR01DA045771 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI KIRBY, LYNN G · 2019 to 2023
$1.9M
Exploring Sex-Differences and a Role for the 5-HT System in Early-Life Stress-Induced Compulsive Ethanol Consumption in AdulthoodF31AA030477 · NIAAA · TEMPLE UNIV OF THE COMMONWEALTH · PI MCELROY, BRYAN D · 2022 to 2023
$66k
NIAAA NIH HHS F31 AA030477NIDA NIH HHS P30 DA013429NIDA NIH HHS R01 DA045771NIDA NIH HHS T32 DA007237
6 · The paper itself

Abstract

Alcohol use disorder (AUD) is a debilitating psychiatric disorder characterized by drinking despite negative social and biological consequences. AUDs make up 71% of substance use disorders, with relapse rates as high as 80%. Current treatments stem from data conducted largely in males and fail to target the psychological distress motivating drinking in stress-vulnerable and at-risk populations. Here we employed a rat model and hypothesized that early life stress would reveal sex differences in ethanol intake and drinking despite negative consequences in adulthood. Rats were group housed or isolated postweaning to evaluate sex and stress effects on ethanol consumption in homecage drinking, self-administration (SA), and punished SA (drinking despite negative consequences) in adulthood. Stressed rats showed elevated homecage ethanol intake, an effect more pronounced in females. During SA, males were more sensitive to stress-induced elevations of drinking over time, but females drank more overall. Stressed rats, regardless of sex, responded more for ethanol than their non-stressed counterparts. Stressed females showed greater resistance to punishment-suppressed SA than stressed males, indicating a more stress-resistant drinking phenotype. Results support our hypothesis that adolescent social isolation stress enhances adult ethanol intake in a sex- and model-dependent manner with females being especially sensitive to early life stress-induced elevations in ethanol intake and punished SA in adulthood. Our findings echo the clinical literature which indicates that stress-vulnerable populations are more likely to 'self-medicate' with substances. Elucidating a potential mechanism that underlies why vulnerable populations 'self-medicate' with alcohol can lead towards developing catered pharmacotherapeutics that could reduce punishment-resistant drinking and relapse.

Indexed as

Alcohol DrinkingEthanolSelf AdministrationSex CharacteristicsSocial IsolationStress, PsychologicalAnimalsCentral Nervous System DepressantsDisease Models, AnimalFemaleMalePunishmentRatsCentral Nervous System DepressantsEthanolEarly life stressEthanolOperant conditioningPunishment-resistant drinkingSex differences

Identifiers

PMID37573960
PMCPMC10592127

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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.