Evidence map›Paper›PMID 31521175›Full record

ArticleLipids in health and disease2019

Variations in hepatic lipid species of age-matched male mice fed a methionine-choline-deficient diet and housed in different animal facilities.

Lisa Rein-Fischboeck, Elisabeth M Haberl, Rebekka Pohl, Susanne Feder, Gerhard Liebisch, Sabrina Krautbauer, Christa Buechler

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Lisa Rein-FischboeckDepartment of Internal Medicine I, Regensburg University Hospital, D-93042, Regensburg, Germany.
Elisabeth M HaberlDepartment of Internal Medicine I, Regensburg University Hospital, D-93042, Regensburg, Germany.
Rebekka PohlDepartment of Internal Medicine I, Regensburg University Hospital, D-93042, Regensburg, Germany.
Susanne FederDepartment of Internal Medicine I, Regensburg University Hospital, D-93042, Regensburg, Germany.
Gerhard LiebischInstitute of Clinical Chemistry and Laboratory Medicine, Regensburg University Hospital, Regensburg, Germany.
Sabrina KrautbauerInstitute of Clinical Chemistry and Laboratory Medicine, Regensburg University Hospital, Regensburg, Germany.
Christa BuechlerDepartment of Internal Medicine I, Regensburg University Hospital, D-93042, Regensburg, Germany. christa.buechler@klinik.uni-regensburg.de.ORCID http://orcid.org/0000-0002-5635-3994
University Hospital Regensburg · DE

Funding

Deutsche Forschungsgemeinschaft BU 1141/12-1 BU 1141/13-1
6 · The paper itself

Abstract

backgroundNon-alcoholic steatohepatitis (NASH) is a common disease and feeding mice a methionine-choline-deficient (MCD) diet is a frequently used model to study its pathophysiology. Genetic and environmental factors influence NASH development and liver lipid content, which was studied herein using C57BL/6 J mice bred in two different animal facilities.

methodsAge-matched male C57BL/6 J mice bred in two different animal facilities (later on referred to as WT1 and WT2) at the University Hospital of Regensburg were fed identical MCD or control chows for 2 weeks. Hepatic gene and protein expression and lipid composition were determined.

resultsNASH was associated with increased hepatic triglycerides, which were actually higher in WT1 than WT2 liver in both dietary groups. Cholesterol contributes to hepatic injury but was only elevated in WT2 NASH liver. Ceramides account for insulin resistance and cell death, and ceramide species d18:1/16:0 and d18:1/18:0 were higher in the NASH liver of both groups. Saturated sphingomyelins only declined in WT1 NASH liver. Lysophosphatidylcholine concentrations were quite normal in NASH and only one of the 12 altered phosphatidylcholine species declined in NASH liver of both groups. Very few phosphatidylethanolamine, phosphatidylserine, and phosphatidylinositol species were comparably regulated in NASH liver of both animal groups. Seven of these lipid species declined and two increased in NASH. Notably, hepatic mRNA expression of proinflammatory (F4/80, CD68, IL-6, TNF and chemerin) and profibrotic genes (TGF beta and alpha SMA) was comparable in WT1 and WT2 mice.

conclusionsMice housed and bred in different animal facilities had comparable disease severity of NASH whereas liver lipids varied among the groups. Thus, there was no specific lipid signature for NASH in the MCD model.

Indexed as

ActinsAnimal ExperimentationAnimalsCalcium-Binding ProteinsCeramidesCholesterolCholine DeficiencyDietDisease Models, AnimalGene Expression RegulationInterleukin-6LiverLysophosphatidylcholinesMaleMethionineMiceActinsAdgre1 protein, mousealpha-smooth muscle actin, mouseCalcium-Binding ProteinsCeramidesCholesterolInterleukin-6interleukin-6, mouseLysophosphatidylcholinesMethioninephosphatidylethanolaminePhosphatidylethanolaminesPhosphatidylinositolsPhosphatidylserinesReceptors, G-Protein-CoupledSphingomyelinsTransforming Growth Factor betaTriglyceridesCeramideChemerin, PhosphatidylcholineCholesterol

Identifiers

PMID31521175
PMCPMC6745065
OpenAlexW2972532512

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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 OpenQuestion graph.