Evidence map›Paper›PMID 32724826›Full record

ArticleJournal of diabetes research2020

A Network-Based Approach to Explore the Mechanism and Bioactive Compounds of Erzhi Pill against Metabolic Dysfunction-Associated Fatty Liver Disease.

Shaojie Huang, Fei Mu, Fei Li, Wenjun Wang, Haixia Chen, Lu Lei, Yang Ma, Yi Ding, Jingwen Wang

Abstract read
In one paragraph

Article in Journal of diabetes research, 2020. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
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.

Shaojie HuangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.ORCID https://orcid.org/0000-0002-6400-7389
Fei MuDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.ORCID https://orcid.org/0000-0001-5706-8864
Fei LiDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Wenjun WangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Haixia ChenDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Lu LeiDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Yang MaDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.
Yi DingDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.ORCID https://orcid.org/0000-0002-2158-3108
Jingwen WangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.ORCID https://orcid.org/0000-0002-3450-9046

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erzhi pill (EZP), a classical traditional Chinese medicine prescription, exerts a potent hepatoprotective effect against metabolic dysfunction-associated fatty liver disease (MAFLD), previously known as nonalcoholic fatty liver disease (NAFLD). However, the mechanism and bioactive compounds underlying the hepatoprotective effect of EZP have not been fully elucidated. In this study, a systematic analytical platform was built to explore the mechanism and bioactive compounds of EZP against MAFLD. This was carried out through target prediction, protein-protein interaction (PPI) network construction, gene ontology, KEGG pathway enrichment, and molecular docking. According to the topological parameters of the PPI network, compound-target-pathway network, 9 targets, and 11 bioactive compounds were identified as core targets and bioactive compounds for molecular docking. The results showed that EZP exerts anti-MAFLD effects through a multicomponent, multitarget, multipathway manner, and luteolin and linarin may be the bioactive compounds of EZP. This study provides further research insights and helps explore the hepatoprotective mechanism of EZP.

Indexed as

Molecular Docking SimulationProtein Interaction MapsDrugs, Chinese HerbalHumansLiverMedicine, Chinese TraditionalNon-alcoholic Fatty Liver DiseaseDrugs, Chinese Herbalerzhi pill

Identifiers

PMID32724826
PMCPMC7382733

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.