Evidence map›Paper›PMID 36687218›Full record

ArticleMediators of inflammation2023

Integrative Analysis of Transcriptome and Metabolome to Illuminate the Protective Effects of Didymin against Acute Hepatic Injury.

Lijun Pang, Yuhua Xiong, Zhongwen Feng, Cuiyu Li, Bin Fang, Quanfang Huang, Xing Lin

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. 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

7 authors at 2 institutions in 1 country.

Lijun PangGuangxi Medical University, Nanning 530021, China.
Yuhua XiongGuangxi Medical University, Nanning 530021, China.ORCID https://orcid.org/0000-0002-3215-4157
Zhongwen FengGuangxi Medical University, Nanning 530021, China.
Cuiyu LiGuangxi Medical University, Nanning 530021, China.
Bin FangGuangxi Medical University, Nanning 530021, China.
Quanfang HuangThe First Affiliated Hospital of Guangxi University of Chinese Medicine, Nanning 530023, China.ORCID https://orcid.org/0000-0002-9008-8741
Xing LinGuangxi Medical University, Nanning 530021, China.ORCID https://orcid.org/0000-0002-9794-829X
Guangxi Medical University · CNGuangxi University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Based on the multiomics analysis, this study is aimed at investigating the underlying mechanism of didymin against acute liver injury (ALI). The mice were administrated with didymin for 2 weeks, followed by injection with lipopolysaccharide (LPS) plus D-galactosamine (D-Gal) to induce ALI. The pathological examination revealed that didymin significantly ameliorated LPS/D-Gal-induced hepatic damage. Also, it markedly reduced proinflammatory cytokines release by inhibiting the TLR4/NF-

Indexed as

NF-kappa BProto-Oncogene Proteins c-akt1-Acylglycerophosphocholine O-AcyltransferaseAnimalsFlavonoidsGlycerophospholipidsGlycosidesGroup IV Phospholipases A2LipopolysaccharidesLiverMetabolomeMicePhosphatidylinositol 3-KinasesToll-Like Receptor 4Transcriptome1-Acylglycerophosphocholine O-AcyltransferasedidyminFlavonoidsGlycerophospholipidsGlycosidesGroup IV Phospholipases A2LipopolysaccharidesLPCAT3 protein, mouseNF-kappa BPhosphatidylinositol 3-KinasesPla2g4b protein, mouseProto-Oncogene Proteins c-aktToll-Like Receptor 4

Identifiers

PMID36687218
PMCPMC9851790
OpenAlexW4315777241

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.