Evidence map›Paper›PMID 41519234›Full record

ArticleThe Journal of nutrition2026

Dietary Ethanolamine Increases Hepatic Lipid Accumulation in Mice Fed a High-Fat Diet.

Courtney M Holdaway, Amy Vo, Kelly-Ann Leonard, Randal Nelson, Aducio Thiesen, Yi Fan, Camila S Marcolla, Robin D Clugston, Benjamin P Willing, Rene L Jacobs

Abstract read
In one paragraph

Article in The Journal of nutrition, 2026. 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
–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

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

10 authors.

Courtney M HoldawayDepartment of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada.
Amy VoDepartment of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada.
Kelly-Ann LeonardDepartment of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada.
Randal NelsonDepartment of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada.
Aducio ThiesenDepartment of Laboratory Medicine, University of Alberta, Edmonton, Canada.
Yi FanDepartment of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada; Agricultural and Agri-food Canada, Lacombe, Alberta, Canada.
Camila S MarcollaDepartment of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada.
Robin D ClugstonDepartment of Physiology, University of Alberta, Edmonton, Canada.
Benjamin P WillingDepartment of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada.
Rene L JacobsDepartment of Agricultural, Food & Nutritional Science, University of Alberta, Edmonton, Canada. Electronic address: rjacobs@ualberta.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEthanolamine (Etn), a precursor of phosphatidylethanolamine (PE), may alter hepatic lipid homeostasis and gut health; its dietary effects remain undefined.

objectiveThe objective of this study was to determine the effects of dietary Etn on lipid and glucose metabolism and liver/gut health in high-fat diet (HFD)-fed mice, complemented by in vitro hepatocyte assays.

methodsTen-wk-old C57BL/6 mice (20 male, 18 female) were fed ad libitum HFD (45% energy from fat) with [Ethanolamine supplementation (ES-group)] or without (CON-group) Etn (8 g/kg diet) for 10 wk. Outcomes included body/liver weight, glucose tolerance test (GTT) results, plasma phosphatidylcholine (PC)/cholesteryl ester (CE)/triacylglycerol (TG) concentrations, hepatic TG/PC/PE concentrations, hepatic endoplasmic reticulum (ER)-stress, and inflammation markers, jejunal morphology/barrier/inflammation genes, and fecal microbiota (α/β diversity). HuH7 cells received 20 μM or 5 mM Etn to assess TG/PC/PE synthesis. STATISTICS: repeated-measures analysis of variance (ANOVA) (GTT), t-test or Wilcoxon (other endpoints), permutational multivariate analysis of variance (PERMANOVA) (β diversity); α=0.05.

resultsES increased hepatic TG in females by 230% compared with CON (P = 0.001), and trended higher in males (P = 0.054); hepatic PC and PE masses were unchanged. In ES males, GTT area under the curve decreased by 22.6% (P = 0.037), and plasma PC, CE, and TG were reduced by: PC -16.6%, CE -24.5%, TG -25.9%, respectively (all P < 0.05). ES males showed higher hepatic Tnf and Cd68 and increased C/EBP homologous protein (CHOP) (all P < 0.05). In vitro, Etn did not alter hepatocellular TG, PC, or PE synthesis (all P > 0.05). Female ES mice exhibited altered fecal β-diversity (PERMANOVA P = 0.006) with early jejunal inflammatory signals (Tnf ↑; P = 0.055).

conclusionsDietary Etn modifies hepatic lipid storage and gut microbiota in a sex-dependent manner and improves glucose tolerance in males, whereas in vitro data indicate no direct effect on hepatocyte lipid synthesis.

Indexed as

Diet, High-FatEthanolamineLipid MetabolismLiverAnimalsEndoplasmic Reticulum StressFemaleGastrointestinal MicrobiomeHepatocytesHumansMaleMiceMice, Inbred C57BLEthanolamineethanolaminemetabolic dysfunction-associated steatotic liver disease (MASLD)microbiomephosphatidylethanolamine (PE)phospholipids

Identifiers

PMID41519234
PMCPMC13014508

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.