Evidence map›Paper›PMID 26088166›Full record

ArticleBrain pathology (Zurich, Switzerland)2016

Astrocyte Dysfunction Induced by Alcohol in Females but Not Males.

Clare J Wilhelm, Joel G Hashimoto, Melissa L Roberts, Shelley H Bloom, Melissa R Andrew, Kristine M Wiren

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

55 citing papers in PubMed, 69 citations in OpenAlex.

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  13. Effect of menstrual cycle on rewarding properties of alcohol cues in women.Psychology of addictive behaviors : journal of the Society of Psychologists in Addictive Behaviors · 2024
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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

6 authors at 3 institutions in 1 country.

Clare J WilhelmVA Portland Health Care System, Portland, OR.
Joel G HashimotoVA Portland Health Care System, Portland, OR.
Melissa L RobertsVA Portland Health Care System, Portland, OR.
Shelley H BloomVA Portland Health Care System, Portland, OR.
Melissa R AndrewCincinnati Center for Growth Disorders, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Kristine M WirenVA Portland Health Care System, Portland, OR.
VA Portland Health Care System · USOregon Health & Science University · USCincinnati Children's Hospital Medical Center · US

Funding

Translational measures of risk for excessive alcohol consumptionP60AA010760 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI TAMARA J. PHILLIPS · 2006 to 2026
$34.5M
Mouse Genetic Models for Alcohol ResearchR24AA020245 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI PHILLIPS, TAMARA J. · 2011 to 2020
$2.3M
Epigenetics underlies long-term risk of relapse during abstinenceR01AA021468 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI GUIZZETTI, MARINA · 2013 to 2017
$1.5M
Sex dependent astrocyte activation and alcohol-induced neurotoxicityR21AA018420 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI WIREN, KRISTINE M. · 2009 to 2010
$346k
BLRD VA I01 BX001172BLRD VA IK2 BX001294NIAAA NIH HHS P60 AA010760NIAAA NIH HHS R01 AA021468NIAAA NIH HHS R21 AA018420NIAAA NIH HHS R24 AA020245
6 · The paper itself

Abstract

Chronic alcohol abuse is associated with brain damage in a sex-specific fashion, but the mechanisms involved are poorly described and remain controversial. Previous results have suggested that astrocyte gene expression is influenced by ethanol intoxication and during abstinence in vivo. Here, bioinformatic analysis of astrocyte-enriched ethanol-regulated genes in vivo revealed ubiquitin pathways as an ethanol target, but with sexually dimorphic cytokine signaling and changes associated with brain aging in females and not males. Consistent with this result, astrocyte activation was observed after exposure in female but not male animals, with reduced S100β levels in the anterior cingulate cortex and increased GFAP(+) cells in the hippocampus. In primary culture, the direct effects of chronic ethanol exposure followed by recovery on sex-specific astrocyte function were examined. Male astrocyte responses were consistent with astrocyte deactivation with reduced GFAP expression during ethanol exposure. In contrast, female astrocytes exhibited increased expression of Tnf, reduced expression of the neuroprotective cytokine Tgfb1, disrupted bioenergetics and reduced excitatory amino acid uptake following exposure or recovery. These results indicate widespread astrocyte dysfunction in ethanol-exposed females and suggest a mechanism that may underlie increased vulnerability to ethanol-induced neurotoxicity in females.

Indexed as

Sex CharacteristicsAnimalsAstrocytesCentral Nervous System DepressantsEthanolFemaleGene Expression ProfilingHippocampusMaleMiceTranscriptomeCentral Nervous System DepressantsEthanolalcoholastrocyteglutamate uptakesexually dimorphictumor necrosis factor

Identifiers

PMID26088166
PMCPMC8028916
OpenAlexW1515859801

What OpenQuestion holds

Textmetadata
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.