Evidence map›Paper›PMID 19170661›Full record

ArticleAlcoholism, clinical and experimental research2009

Quantitative lipid metabolomic changes in alcoholic micropigs with fatty liver disease.

Angela M Zivkovic, J Bruce German, Farah Esfandiari, Charles H Halsted

Abstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

  1. Methionine metabolism, functions, and application in swine.Animal nutrition (Zhongguo xu mu shou yi xue hui) · 2025
    Review
  2. Review
  3. Preparation of Active Peptides fromMolecules (Basel, Switzerland) · 2022
    Article
  4. DNA Methylation in Nonalcoholic Fatty Liver Disease.International journal of molecular sciences · 2020
    Review
  5. Review
  6. Article
  7. Molecular Pathogenesis of NASH.International journal of molecular sciences · 2016
    Review
  8. Potential epigenetic mechanism in non-alcoholic Fatty liver disease.International journal of molecular sciences · 2015
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Nutritional deficiencies and phospholipid metabolism.International journal of molecular sciences · 2011
    Review
  15. Metabolomics for assessment of nutritional status.Current opinion in clinical nutrition and metabolic care · 2009
    Review
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 at 1 institution in 1 country.

Angela M ZivkovicDepartment of Entomology, University of California Davis, Davis, California 95616, USA. amzivkovic@ucdavis.edu
J Bruce German
Farah Esfandiari
Charles H Halsted
University of California, Davis · US

Funding

Workshop on Environmental Technology Transfer and EntrepreneurshipP42ES004699 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI VASYLIEVA, NATALIA · 1987 to 2021
$50.1M
UC Davis Center for Children's Environmental Health (CCEH)P01ES011269 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI VAN DE WATER, JUDY A. · 2001 to 2018
$12.5M
NIEHS Center for Health Effects of AgrochemicalsP30ES005707 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI MATSUMURA, FUMIO NONE · 1992 to 2006
$9.9M
NIAAA NIH HHS AA RO-114545NIEHS NIH HHS P01 ES011269NIEHS NIH HHS P01 ES11269NIEHS NIH HHS P30 ES005707NIEHS NIH HHS P42 ES004699NIEHS NIH HHS P42 ES04699
6 · The paper itself

Abstract

backgroundChronic ethanol consumption coupled with folate deficiency leads to rapid liver fat accumulation and progression to alcoholic steatohepatitis (ASH). However, the specific effects of alcohol on key liver lipid metabolic pathways involved in fat accumulation are unknown. It is unclear whether lipid synthesis, lipid export, or a combination of both is contributing to hepatic steatosis in ASH.

methodsIn this study we estimated the flux of fatty acids (FA) through the stearoyl-CoA desaturase (SCD), phosphatidylethanolamine-N-methyltransferase (PEMT), and FA elongation pathways in relation to liver triacylglycerol (TG) content in Yucatan micropigs fed a 40% ethanol folate-deficient diet with or without supplementation with S-adenosyl methionine (SAM) compared with controls. Flux through the SCD and PEMT pathways was used to assess the contribution of lipid synthesis and lipid export respectively on the accumulation of fat in the liver. Liver FA composition within TG, cholesterol ester (CE), phosphatidylethanolamine, and phosphatidylcholine classes was quantified by gas chromatography.

resultsAlcoholic pigs had increased liver TG content relative to controls, accompanied by increased flux through the SCD pathway as indicated by increases in the ratios of 16:1n7 to 16:0 and 18:1n9 to 18:0. Conversely, flux through the elongation and PEMT pathways was suppressed by alcohol, as indicated by multiple metabolite ratios. SAM supplementation attenuated the TG accumulation associated with alcohol.

conclusionsThese data provide an in vivo examination of liver lipid metabolic pathways confirming that both increased de novo lipogenesis (e.g., lipid synthesis) and altered phospholipid metabolism (e.g., lipid export) contribute to the excessive accumulation of lipids in liver affected by ASH.

Indexed as

MetabolomicsAlcoholismAnimalsCholesterol EstersDisease Models, AnimalEthanolFatty AcidsFatty LiverFatty Liver, AlcoholicLipid MetabolismMalePhosphatidylcholinesPhosphatidylethanolamine N-MethyltransferasePhosphatidylethanolaminesStearoyl-CoA DesaturaseSwineCholesterol EstersEthanolFatty AcidsPhosphatidylcholinesphosphatidylethanolaminePhosphatidylethanolamine N-MethyltransferasePhosphatidylethanolaminesStearoyl-CoA DesaturaseTriglycerides

Identifiers

PMID19170661
PMCPMC3939313
OpenAlexW1995773171

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.