Evidence map›Paper›PMID 35790996›Full record

ArticleNutrition & metabolism2022

Absolute quantitative lipidomics reveals lipids profiling in liver of mice with early-stage alcoholic liver disease.

Fei Zhao, Jun Chen, Rui Guo, Jinyan Zhu, Weijia Gu, Songtao Li, Jiaomei Li

Open access · goldAbstract read
In one paragraph

Article in Nutrition & metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  7. Liquid Chromatography/Tandem Mass Spectrometry Analysis ofAntioxidants (Basel, Switzerland) · 2024
    Article
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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.

Fei Zhao *School of Public Health, Zhejiang Chinese Medical University, 488 Binwen Road, Hangzhou, 310053, China.
Jun Chen *School of Public Health, Zhejiang Chinese Medical University, 488 Binwen Road, Hangzhou, 310053, China.
Rui GuoSchool of Public Health, Zhejiang Chinese Medical University, 488 Binwen Road, Hangzhou, 310053, China.
Jinyan ZhuSchool of Public Health, Zhejiang Chinese Medical University, 488 Binwen Road, Hangzhou, 310053, China.
Weijia GuSchool of Public Health, Zhejiang Chinese Medical University, 488 Binwen Road, Hangzhou, 310053, China.
Songtao LiSchool of Public Health, Zhejiang Chinese Medical University, 488 Binwen Road, Hangzhou, 310053, China. lisongtao@zcmu.edu.cn.
Jiaomei LiSchool of Public Health, Zhejiang Chinese Medical University, 488 Binwen Road, Hangzhou, 310053, China. jiaomeili90@163.com.
Zhejiang Chinese Medical University · CN

Funding

National Natural Science Foundation of China 82103843Research Project of Zhejiang Chinese Medical University 2021RCZXZK13Special Support Program for High Level Talents in Zhejiang Province ZJWR0308092
6 · The paper itself

Abstract

backgroundAlcoholic liver disease (ALD) is one of the most prevalent chronic liver disease worldwide. Alcohol-induced alterations in hepatic lipids play an important role in ALD develpoment and progression. The present study aimed to thoroughly describe the changes of lipid profiling in liver of mice with early-stage alcoholic liver disease.

methodsC57BL/6J male mice aged 7-week were randomized into alcohol-fed (AF) group and pair-fed control group (PF) (n = 10 per group). The early stage of ALD was induced with Lieber-DeCarli liquid diet. The lipids profiling was analyzed by absolute quantitative lipidomics with UHPLC-QTRAP-MS/MS.

resultsAlcohol intake significantly increased the levels of alanine aminotransferase (ALT) in plasma, and tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and triacylglycerols (TAG) levels in liver. Lipidomis analyses showed that 41 TAGs were up-regulated and 8 TAGs were down-regulated in response to alcohol intake. The 8 decreased TAGs were with more double bond, longer carbon chain length and mostly contained docosahexaenoic acid (C22:6n-3) and eicosapentaenoic acid (C20:5n-3), compared with the up-regulated TAGs. Furthermore, the down-regulated TAG(56:9)_FA20:5 was inversely associated with ALT and IL-6 levels. In addition, several altered lysophosphatidylcholines (LPC), lysophosphatidylethanolamines (LPE) and hexosylceramides (HCER) were all significantly decreased in response to alcohol consumption, especially HCer(18:1/22:0), with the top reduction among all the down-regulated lipids.

conclusionsThese findings suggest that not only the up-regulated lipids, alcohol-induced reduction in some specific lipids might also contribute to the ALD development, especially TAG(56:9)_FA20:5 and HCer(18:1/22:0). Their physiological functions and effects on ALD development warrants further investigation.

Indexed as

Alcoholic liver diseaseAlcohol intakeFree fatty acidsLipidomicsTriglyceride

Identifiers

PMID35790996
PMCPMC9254412
OpenAlexW4283821231

What OpenQuestion 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 OpenQuestion graph.