Evidence map›Paper›PMID 36462937›Full record

ArticleAlcohol, clinical & experimental research2023

Influence of early-life adversity on responses to acute and chronic ethanol in female mice.

Agbonlahor Okhuarobo, Maggie Angelo, Jessica L Bolton, Catherine Lopez, Ighodaro Igbe, Tallie Z Baram, Candice Contet

Open access · hybridAbstract read
In one paragraph

Article in Alcohol, clinical & experimental research, 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
1.2field-weighted citation impact, top 26% of its field
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, 10 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. KAlcohol (Fayetteville, N.Y.) · 2025
    Article
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  11. Chronic MAP4343 reverses escalated alcohol drinking in a mouse model of alcohol use disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
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 at 4 institutions in 2 countries.

Agbonlahor OkhuaroboDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, California, USA.
Maggie AngeloDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, California, USA.
Jessica L BoltonDepartments of Anatomy/Neurobiology and Pediatrics, University of California-Irvine, Irvine, California, USA.
Catherine LopezDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, California, USA.
Ighodaro IgbeDepartment of Pharmacology & Toxicology, Faculty of Pharmacy, University of Benin, Benin City, Nigeria.
Tallie Z BaramDepartments of Anatomy/Neurobiology and Pediatrics, University of California-Irvine, Irvine, California, USA.
Candice ContetDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, California, USA.ORCID 0000-0002-4459-9540
Scripps Research Institute · USGeorgia State University · USUniversity of Benin · NGUniversity of California, Irvine · US

Funding

Viral Vector CoreP60AA006420 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI AMANDA J ROBERTS · 2003 to 2026
$46.3M
SYSTEMIC NEUROPHARMACOLOGYP50AA006420 · NIAAA · SCRIPPS RESEARCH INSTITUTE · PI RIVIER, CATHERINE L · 1985 to 2002
$5.1M
Activation of the parasubthalamic nucleus in alcohol dependenceR01AA026685 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI Jeffery Lee Dunning · 2018 to 2026
$3.0M
Adaptations to chronic activation of BK channels by ethanol: Contribution to dependence and toleranceR33AA027636 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI CONTET, CANDICE · 2022 to 2024
$1.6M
Novel circuit mechanism of alcohol dependence vulnerability following early-life adversityR21AA027372 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI CONTET, CANDICE · 2020 to 2021
$476k
Adaptations to chronic activation of BK channels by ethanol: Contribution to dependence and toleranceR21AA027636 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI CONTET, CANDICE · 2020 to 2021
$473k
NIAAA NIH HHS P50 AA006420NIAAA NIH HHS P60 AA006420NIAAA NIH HHS R01 AA026685NIAAA NIH HHS R21 AA027372NIAAA NIH HHS R21 AA027636NIAAA NIH HHS R33 AA027636
6 · The paper itself

Abstract

backgroundStressful early-life experiences increase the risk of developing an alcohol use disorder. We previously found that male C57BL/6J mice reared under limited bedding and nesting (LBN) conditions, a model of early-life adversity, escalate their ethanol intake in limited-access two-bottle choice (2BC) sessions faster than control (CTL)-reared counterparts when exposed to chronic intermittent ethanol (CIE) vapor inhalation. However, the alcohol consumption of female littermates was not affected by LBN or CIE. In the present study, we sought to determine whether this phenotype reflected a general insensitivity of female mice to the influence of early-life stress on alcohol responses.

methodsIn a first experiment, CTL and LBN females with a history of 2BC combined or not with CIE were tested in affective and nociceptive assays during withdrawal. In a second group of CTL and LBN females, we examined ethanol-induced antinociception, sedation, plasma clearance, and c-Fos induction.

resultsIn females withdrawn from chronic 2BC, CIE increased digging, reduced grooming, and increased immobility in the tail suspension test regardless of early-life history. In contrast, LBN rearing lowered mechanical nociceptive thresholds regardless of CIE exposure. In females acutely treated with ethanol, LBN rearing facilitated antinociception and delayed the onset of sedation without influencing ethanol clearance rate or c-Fos induction in the paraventricular nucleus of the hypothalamus, paraventricular nucleus of the thalamus, central nucleus of the amygdala, or auditory cortex.

conclusionCIE withdrawal produced multiple indices of negative affect in C57BL/6J females, suggesting that their motivation to consume alcohol may differ from air-exposed counterparts despite equivalent intake. Contrasted with our previous findings in males, LBN-induced mechanical hyperalgesia in chronic alcohol drinkers was specific to females. Lower nociceptive thresholds combined with increased sensitivity to the acute antinociceptive effect of ethanol may contribute to reinforcing ethanol consumption in LBN females but are not sufficient to increase their intake.

Indexed as

AlcoholismStress, PsychologicalAlcohol DrinkingAnimalsEthanolFemaleMiceMice, Inbred C57BLProto-Oncogene Proteins c-fosEthanolProto-Oncogene Proteins c-fosearly-life stresshyperkatifeiapainresiliencevulnerability

Identifiers

PMID36462937
PMCPMC9992294
OpenAlexW4310668245

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.