Evidence map›Paper›PMID 40757754›Full record

ArticleAlcohol, clinical & experimental research2025

High-throughput quantitation of acetaldehyde and ethanol in mice using gas chromatography/mass spectrometry positive chemical ionization.

Yu-Hong Lin, Cheng Chen, Shoupeng Wei, Guillot Adrien, Bryan Mackowiak, Hongna Pan, Yaojie Fu, Luca Maccioni, Tianyi Ren, Li Zhang and 3 more

Abstract read
In one paragraph

Article in Alcohol, clinical & experimental research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

13 authors.

Yu-Hong LinLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.ORCID 0009-0002-3458-799X
Cheng ChenLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.
Shoupeng WeiLaboratory of Integrative Neuroscience, NIAAA/NIH, Bethesda, Maryland, USA.
Guillot AdrienLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.ORCID 0000-0002-6002-9986
Bryan MackowiakLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.ORCID 0000-0001-9840-2013
Hongna PanLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.
Yaojie FuLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.
Luca MaccioniLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.
Tianyi RenLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.
Li ZhangLaboratory of Integrative Neuroscience, NIAAA/NIH, Bethesda, Maryland, USA.
Joseph HibbelnUniversity of Bristol, Bristol, UK.
Robert PawloskyOffice of Scientific Director, DICBR, NIAAA/NIH, Bethesda, Maryland, USA.
Bin GaoLaboratory of Liver Diseases, NIAAA/NIH, Bethesda, Maryland, USA.

Funding

Immunity, liver injury and repairZ01AA000368 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI GAO, BIN · 2002 to 2008
$1.2M
Intramural NIH HHS Z01 AA000368NIAAA NIH HHS AA000368
6 · The paper itself

Abstract

backgroundAcetaldehyde, an immediate ethanol metabolite, mediates many ethanol-induced behavioral effects and is both psychoactive and toxic to animals and humans. Monitoring the kinetics of acetaldehyde using rodent models of alcohol misuse is essential for understanding and managing ethanol-associated diseases. However, quantitation of acetaldehyde in biological specimens after alcohol consumption has been challenging due to its high volatility, relatively low concentrations, and strong reactivity toward biochemical molecules. It was necessary to develop and establish an accurate and high-throughput method to quantitate acetaldehyde and ethanol.

methodsGas chromatography/mass spectrometry in positive chemical ionization mode coupled with a 111-vial headspace autosampler was employed to quantitate acetaldehyde and ethanol using

resultsThe method was validated and applied to quantitate acetaldehyde and ethanol in blood and tissues from multiple mouse studies on ethanol metabolism. Acetaldehyde and ethanol were well-resolved from chromatographic interferences with linear ranges of 6.25-800 μM for acetaldehyde and 1.25-160 mM for ethanol. Both regression coefficients for calibration curves were >0.999. The within- and between-run precisions for ethanol in plasma, whole blood, and serum were all <5.0%, and for acetaldehyde in plasma and serum were <9.0%, while in whole blood it was 19.2%. Sample throughput was on the order of 60 samples per 15 h daily, with a maximum of 111 per batch.

conclusionsDespite some limitations, this validated method proved to be specific, accurate, and reproducible for high-throughput quantitation of acetaldehyde and ethanol in rodent plasma, whole blood, serum, and visceral organs.

Indexed as

AcetaldehydeEthanolGas Chromatography-Mass SpectrometryHigh-Throughput Screening AssaysAnimalsMaleMiceMice, Inbred C57BLAcetaldehydeEthanoldirect PCA procedureplasmaselected ion monitoringserumwhole blood

Identifiers

PMID40757754
PMCPMC12463767

What Socratic holds

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LicenceCC BY
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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 Socratic graph.