Evidence map›Paper›PMID 28839246›Full record

ArticleScientific reports2017

Activation of autophagy attenuates EtOH-LPS-induced hepatic steatosis and injury through MD2 associated TLR4 signaling.

Xiaoxia Kong, Ying Yang, Li Ren, Tuo Shao, Fengyuan Li, Cuiqing Zhao, Liming Liu, Hongyu Zhang, Craig J McClain, Wenke Feng

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  13. Autophagy in liver diseases.World journal of hepatology · 2021
    Review
  14. Article
  15. Hepatoprotective Effects of theEvidence-based complementary and alternative medicine : eCAM · 2021
    Article
  16. Article
  17. Oxidative medicine and cellular longevity · 2020
    Article
  18. Review
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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

10 authors at 2 institutions in 2 countries.

Xiaoxia KongSchool of Basic Medical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China. kongxx@wmu.edu.cn.
Ying YangSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Li Ren1st Affiliate Hospital, Xi'an Jiaotong University, Xi'an, China.
Tuo ShaoDepartments of Pharmacology and Toxicology and Medicine, University of Louisville Alcohol Research Center, University of Louisville Hepatobiology & Toxicology Program, University of Louisville, Louisville, USA.
Fengyuan LiDepartments of Pharmacology and Toxicology and Medicine, University of Louisville Alcohol Research Center, University of Louisville Hepatobiology & Toxicology Program, University of Louisville, Louisville, USA.
Cuiqing ZhaoSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Liming LiuDepartments of Pharmacology and Toxicology and Medicine, University of Louisville Alcohol Research Center, University of Louisville Hepatobiology & Toxicology Program, University of Louisville, Louisville, USA.
Hongyu ZhangSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Craig J McClainDepartments of Pharmacology and Toxicology and Medicine, University of Louisville Alcohol Research Center, University of Louisville Hepatobiology & Toxicology Program, University of Louisville, Louisville, USA.
Wenke FengSchool of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China. wenke.feng@louisville.edu.
University of Louisville · USWenzhou Medical University · CN

Funding

Mechanisms of Probiotics in Alcoholic Liver DiseaseR01AA023190 · NIAAA · UNIVERSITY OF LOUISVILLE · PI FENG, WENKE · 2015 to 2024
$3.5M
Mechanisms for alcohol induced gut barrier dysfunction in ALDR01AA023681 · NIAAA · UNIVERSITY OF LOUISVILLE · PI MCCLAIN, CRAIG J. · 2014 to 2018
$1.6M
FGF21 and adipose lipolysis in alcoholic fatty liverR21AA022416 · NIAAA · UNIVERSITY OF LOUISVILLE · PI FENG, WENKE · 2014 to 2015
$388k
Dietary Fat and Alcoholic Liver DiseaseI01BX002996 · VA · LOUISVILLE VA MEDICAL MEDICAL CENTER · PI MCCLAIN, CRAIG J. · 2017 to 2020
–
BLRD VA I01 BX002996NIAAA NIH HHS R01 AA023190NIAAA NIH HHS R01 AA023681NIAAA NIH HHS R21 AA022416
6 · The paper itself

Abstract

Autophagy serves as a protective mechanism to degrade damaged organelles and proteins. Acute alcohol exposure is known to activate the hepatic autophagy response, whereas chronic alcohol exposure slows autophagosome formation along with an elevation of gut-derived endotoxin. In the current study, we examined whether lipopolysaccharide (LPS) administration decreased autophagic response in the liver of mice treated by short-term alcohol and whether activation of autophagy by rapamycin attenuates EtOH-LPS-induced liver steatosis and injury. We demonstrated that ten-day alcohol feeding primed the liver to LPS-induced lipid accumulation and liver injury with significantly increased hepatic steatosis and serum AST level as well as hepatic cellular NF-κB activation. LPS increased alcohol-mediated reactive oxygen species (ROS) formation while reducing autophagy activation. These deleterious effects were attenuated by rapamycin administration in mice. The protective effects of rapamycin are associated with decreased cellular MD2/TLR4 expression and interaction in Raw264.7 cells. Taken together, our results demonstrated that enhanced gut-derived LPS decreases the hepatic autophagosome numbers in response to alcohol exposure, and activation of autophagy by rapamycin protects from EtOH-LPS-induced liver injury, probably through reduced macrophage expression and interaction of TLR4/MD2 signaling complex.

Indexed as

AutophagySignal TransductionAnimalsAspartate AminotransferasesEthanolFatty LiverImmunosuppressive AgentsLipopolysaccharidesLymphocyte Antigen 96MiceNF-kappa BRAW 264.7 CellsReactive Oxygen SpeciesSirolimusToll-Like Receptor 4Aspartate AminotransferasesEthanolImmunosuppressive AgentsLipopolysaccharidesLy96 protein, mouseLymphocyte Antigen 96NF-kappa BReactive Oxygen SpeciesSirolimusTlr4 protein, mouseToll-Like Receptor 4

Identifiers

PMID28839246
PMCPMC5571015
OpenAlexW2749083840

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.