Evidence map›Paper›PMID 22307928›Full record

ArticleHepatology (Baltimore, Md.)2012

Interstrain differences in liver injury and one-carbon metabolism in alcohol-fed mice.

Masato Tsuchiya, Cheng Ji, Oksana Kosyk, Svitlana Shymonyak, Stepan Melnyk, Hiroshi Kono, Volodymyr Tryndyak, Levan Muskhelishvili, Igor P Pogribny, Neil Kaplowitz and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Pooled it
  2. Natural variation suggests candidate genes underlying Caenorhabditis elegans susceptibility to diverse toxicants.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  3. Natural variation suggests candidate genes underlyingbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Gut microbiota in liver disease: too much is harmful, nothing at all is not helpful either.American journal of physiology. Gastrointestinal and liver physiology · 2019
    Review
  12. Article
  13. Alcoholic liver disease: Utility of animal models.World journal of gastroenterology · 2018
    Review
  14. Heritability of the aged glutathione phenotype is dependent on tissue of origin.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. 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

11 authors at 5 institutions in 2 countries.

Masato TsuchiyaDepartment of Environmental Sciences and Engineering, University of North Carolina, Chapel Hill, NC 27599, USA.
Cheng Ji
Oksana Kosyk
Svitlana Shymonyak
Stepan Melnyk
Hiroshi Kono
Volodymyr Tryndyak
Levan Muskhelishvili
Igor P Pogribny
Neil Kaplowitz
Ivan Rusyn
University of North Carolina at Chapel Hill · USNational Center for Toxicological Research · USUniversity of Southern California · USUniversity of Arkansas for Medical Sciences · USUniversity of Yamanashi · JP

Funding

USC RESEARCH CENTER FOR LIVER DISEASES: PILOT PROGRAMSP30DK048522 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KAPLOWITZ, NEIL · 1995 to 2020
$21.8M
Homocysteine, ER Stress and Alcoholic Liver Injury.R01AA014428 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JI, CHENG, KAPLOWITZ, NEIL · 2004 to 2014
$3.7M
Bioengineering partnership to improve chemical hazard testing paradigmsR01ES015241 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RUSYN, IVAN · 2008 to 2012
$3.1M
Metabolomic and Toxicogenetic Study of Ethanol ToxicityR01AA016258 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI RUSYN, IVAN · 2005 to 2009
$2.5M
Role of aberrant regulation of organelle stress responses in alcohol-induced liveR01AA018846 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JI, CHENG · 2009 to 2012
$1.5M
Effect of HIV protease inhibitor on alcohol induced ER stress and liver injury.R01AA018612 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JI, CHENG · 2010 to 2013
$1.5M
NIAAA NIH HHS R01 AA014428NIAAA NIH HHS R01 AA016258NIAAA NIH HHS R01 AA018612NIAAA NIH HHS R01 AA018846NIDDK NIH HHS P30 DK048522NIEHS NIH HHS R01 ES015241
6 · The paper itself

Abstract

unlabelledAlcoholic liver injury is a major public health issue worldwide. Even though the major mechanisms of this disease have been established over the past decades, little is known about genetic susceptibility factors that may predispose individuals who abuse alcoholic beverages to liver damage and subsequent pathological conditions. We hypothesized that a panel of genetically diverse mouse strains may be used to examine the role of endoplasmic reticulum (ER) stress and one-carbon metabolism in the mechanism of interindividual variability in alcoholic liver injury. We administered alcohol (up to 27 mg/kg/d) in a high-fat diet using an intragastric intubation model for 28 days to male mice from 14 inbred strains (129S1/SvImJ, AKR/J, BALB/cJ, BALB/cByJ, BTBR T+tf/J, C3H/HeJ, C57BL/10J, DBA/2J, FVB/NJ, KK/HIJ, MOLF/EiJ, NZW/LacJ, PWD/PhJ, and WSB/EiJ). Profound interstrain differences (more than 3-fold) in alcohol-induced steatohepatitis were observed among the strains in spite of consistently high levels of urine alcohol that were monitored throughout the study. We found that ER stress genes were induced only in strains with the most liver injury. Liver glutathione and methyl donor levels were affected in all strains, albeit to a different degree. The most pronounced effects that were closely associated with the degree of liver injury were hyperhomocysteinemia and strain-dependent differences in expression patterns of one-carbon metabolism-related genes.

conclusionOur data demonstrate that strain differences in alcohol-induced liver injury and steatosis are striking and independent of alcohol exposure and the most severely affected strains exhibit major differences in the expression of ER stress markers and genes of one-carbon metabolism.

Indexed as

AlcoholsAnimalsBiopsy, NeedleBlotting, WesternDisease Models, AnimalFatty Liver, AlcoholicImmunohistochemistryLipid PeroxidationMaleMethionineMiceMice, Inbred BALB CMice, Inbred C3HMice, Inbred C57BLMice, Inbred DBAMice, Inbred StrainsAlcoholsMethionineOne-Carbon Group Transferases

Identifiers

PMID22307928
PMCPMC3350836
OpenAlexW2082498487

What OpenQuestion holds

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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.