Evidence map›Paper›PMID 37038793›Full record

ArticleTechnology and health care : official journal of the European Society for Engineering and Medicine2023

Investigation on the mechanism of Ginkgo Folium in the treatment of Non-alcoholic Fatty Liver Disease by strategy of network pharmacology and molecular docking.

Yuanfang Sun, Leqi Wang, Lijing Du, Huajun Yu, Yan Tian, Huizi Jin, Shasha Li, Shikai Yan, Xue Xiao

Open access · bronzeAbstract read
In one paragraph

Article in Technology and health care : official journal of the European Society for Engineering and Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. International journal of molecular sciences · 2026
    Article
  2. Active Components ofAntioxidants (Basel, Switzerland) · 2026
    Article
  3. 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

9 authors at 3 institutions in 1 country.

Yuanfang SunGuangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Leqi WangGuangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Lijing DuSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.
Huajun YuGuizhou Jingcheng Pharmaceutical Co., Ltd., Guiyang, Guizhou, China.
Yan TianGuizhou Jingcheng Pharmaceutical Co., Ltd., Guiyang, Guizhou, China.
Huizi JinSchool of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.
Shasha LiThe Second Clinical College of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Shikai YanGuangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Xue XiaoGuangdong Pharmaceutical University, Guangzhou, Guangdong, China.
Guangzhou University of Chinese Medicine · CNShanghai Jiao Tong University · CNGuangdong Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGinkgo Folium has a favorable effect on non-alcoholic fatty live disease (NAFLD), but its mechanism remains unclear.

objectiveThe aim of this study is to reveal the underlying mechanism of Ginkgo Folium in the treatment of NAFLD.

methodsIngredients of Ginkgo Folium and ingredients-related genes were collected from TCMSP database and SwissTargetPrediction website, respectively. Genecards database was used to obtain NAFLD-related genes. Next, the protein-protein interaction network and key ingredients-genes network were constructed via Cytoscape3.7.0. Based on the Metascape website, gene ontology function analysis and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis were carried out for key genes. Finally, molecular docking was performed to present the interaction between components and genes using AutoDock Vina 1.1.2.

resultsEighteen active ingredients and 10 target genes were screened from Ginkgo Folium. AKT1, TNF, EGFR, PTGS2, MAPK8, PPAγ, APP, ESR1, HIFα and PPAα were considered as potential therapeutic targets. These target genes were mainly enriched in insulin resistance, HIF-1, adipocytokine and AMPK signaling pathways. Molecular docking results suggested that Ginkgo Folium active ingredients including luteolin-4'-glucoside, sesamin, luteolin, chryseriol, isorhamnetin and laricitrin showed strong binding capacities with AKT1.

conclusionThe study showed that multi-components in Ginkgo Folium interacted with AKT1 and regulated AKT-AMPK/HIF pathway to alleviate NAFLD. Our findings provided an essential role and basis for new anti-NAFLD drug discovery and further research on Ginkgo Folium.

Indexed as

Network PharmacologyNon-alcoholic Fatty Liver DiseaseAMP-Activated Protein KinasesGinkgo bilobaHumansLuteolinMolecular Docking SimulationAMP-Activated Protein KinasesLuteolinaction mechanismmolecular dockingnetwork pharmacologynon-alcoholic fatty live disease

Identifiers

PMID37038793
PMCPMC10200225
OpenAlexW4362696364

What OpenQuestion holds

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LicenceCC BY-NC
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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.