Evidence map›Paper›PMID 33517789›Full record

ArticleDrug delivery2021

Study on mechanism of matrine in treatment of COVID-19 combined with liver injury by network pharmacology and molecular docking technology.

Fangzhou Liu, Yuanbai Li, Yang Yang, Meng Li, Yu Du, Yiying Zhang, Jing Wang, Yujing Shi

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
  2. Exploring the Therapeutic Potential ofMolecules (Basel, Switzerland) · 2024
    Article
  3. Article
  4. Potential Hepatoprotective Effects ofAntioxidants (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
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  13. 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

8 authors at 1 institution in 1 country.

Fangzhou LiuInstitute of Information on Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China.
Yuanbai LiInstitute of Information on Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China.
Yang YangInstitute of Information on Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China.
Meng LiInstitute of Information on Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China.
Yu DuInstitute of Information on Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China.
Yiying ZhangInstitute of Information on Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China.
Jing WangInstitute of Information on Traditional Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, China.
Yujing ShiInstitute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to investigate the pharmacological mechanism of matrine in treatment of COVID-19 combined with liver injury. Potential targets related to matrine, COVID-19 and liver injury were identified from several databases. We constructed PPI network and screened the core targets according to the degree value. Then, GO and KEGG enrichment were carried out. Molecular docking technology was used to verify the affinity between matrine and the crystal structure of core target protein. Finally, real-time RT-PCR was used to detect the effects of matrine on hub gene expression in liver tissue of liver injury mice and lung tissue of lung injury mice to further confirm the results of network pharmacological analysis. The results show that six core targets including AKT1, TP53, TNF, IL6, BCL2L1 and ATM were identified. The potential therapeutic mechanism of matrine on COVID-19 combined with liver injury is closely related to regulate antiviral process, improve immune system and regulate the level of inflammatory factors. Molecular docking showed that matrine could spontaneously bind to the receptor protein and had strong binding force. Real-time RT-PCR demonstrated that matrine could significantly reduce the expression of AKT1, TP53, TNF, IL6 and ATM in mice with liver injury or lung injury (P < 0.05), and increase the expression of BCL2L1 to a certain extent (P > 0.05). Our results indicate that matrine can achieve simultaneous intervention of COVID-19 combined with liver injury by multi-dimensional pharmacological mechanism.

Indexed as

COVID-19 Drug TreatmentAlkaloidsAnimalsAntiviral AgentsChemical and Drug Induced Liver InjuryCOVID-19Dose-Response Relationship, DrugHumansLipopolysaccharidesLiverMaleMatrinesMiceMice, Inbred C57BLMolecular Docking SimulationQuinolizinesAlkaloidsAntiviral AgentsLipopolysaccharidesMatrinesQuinolizinesCOVID-19liver injuryMatrinemolecular dockingnetwork pharmacologyreal-time RT-PCR

Identifiers

PMID33517789
PMCPMC8735880
OpenAlexW3126833332

What OpenQuestion holds

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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.