Evidence map›Paper›PMID 32158448›Full record

ArticleFrontiers in immunology2020

Mangiferin Attenuates LPS/D-GalN-Induced Acute Liver Injury by Promoting HO-1 in Kupffer Cells.

Sen Yang, Ge Kuang, Liangke Zhang, Shengwang Wu, Zizuo Zhao, Bin Wang, Xinru Yin, Xia Gong, Jingyuan Wan

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.9field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
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  8. Mangiferin Ameliorates CClJournal of inflammation research · 2024
    Article
  9. Article
  10. Review
  11. Mangiferin: the miraculous xanthone with diverse pharmacological properties.Naunyn-Schmiedeberg's archives of pharmacology · 2023
    Review
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  14. 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

9 authors at 3 institutions in 1 country.

Sen YangChongqing Key Laboratory of Biochemistry and Molecular Pharmacology, Chongqing Medical University, Chongqing, China.
Ge KuangChongqing Key Laboratory of Biochemistry and Molecular Pharmacology, Chongqing Medical University, Chongqing, China.
Liangke ZhangChongqing Key Laboratory of Biochemistry and Molecular Pharmacology, Chongqing Medical University, Chongqing, China.
Shengwang WuDepartment of Anatomy, Chongqing Medical University, Chongqing, China.
Zizuo ZhaoDepartment of Anesthesiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Bin WangDepartment of Anesthesiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Xinru YinDepartment of Gastroenterology, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing, China.
Xia GongDepartment of Anatomy, Chongqing Medical University, Chongqing, China.
Jingyuan WanChongqing Key Laboratory of Biochemistry and Molecular Pharmacology, Chongqing Medical University, Chongqing, China.
Chongqing Medical University · CNDaping Hospital · CNFirst Affiliated Hospital of Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute liver injury and its terminal phase, hepatic failure, trigger a series of complications, including hepatic encephalopathy, systematic inflammatory response syndrome, and multiorgan failure, with relatively high morbidity and mortality. Liver transplantation is the ultimate intervention, but the shortage of donor organs has limited clinical success. Mangiferin (MF), a xanthone glucoside, has been reported to have excellent anti-inflammatory efficacy. Here, a lipopolysaccharide (LPS)/D-galactosamine (D-GalN)-induced acute liver injury mouse model was established to investigate the protective role of MF and the underlying mechanisms of action. Pretreatment with MF improved survival, decreased serum aminotransferase activities, and inhibited hepatic TNF-α production in LPS/D-GalN-challenged mice. Through Kupffer cell (KC) deletion by GdCl

Indexed as

AnimalsAnti-Inflammatory AgentsChemical and Drug Induced Liver InjuryGalactosamineHeme Oxygenase-1Kupffer CellsLipopolysaccharidesLiverMembrane ProteinsMiceMice, Inbred BALB CModels, AnimalNF-kappa BPrimary Cell CultureProtective AgentsSignal TransductionAnti-Inflammatory AgentsGalactosamineHeme Oxygenase-1Hmox1 protein, mouseLipopolysaccharidesmangiferinMembrane ProteinsNF-kappa BProtective AgentsTlr4 protein, mouseToll-Like Receptor 4Tumor Necrosis Factor-alphaXanthonesacute liver injuryheme oxygenase-1 (HO-1)lipopolysaccharide/D-galactosamine (LPS/D-GalN)mangiferinTNF-α

Identifiers

PMID32158448
PMCPMC7052129
OpenAlexW3006690479

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.