Evidence map›Paper›PMID 37606869›Full record

ArticleChinese journal of integrative medicine2023

Network Pharmacology and Experimental Validation to Explore Mechanism of Tetrahydropalmatine on Acute Myocardial Ischemia.

Po-Li Lin, Jun-Ling Cao, Ping Ren, Jia-Li Chen, Bo-Ya Cao, Ping He, Chang-Hui Zheng, Qi-Wen Li, Wei Wang, Jian Zhang

Abstract read
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In one paragraph

Article in Chinese journal of integrative medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.2field-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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 2 institutions in 1 country.

Po-Li LinSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Jun-Ling CaoSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Ping RenSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Jia-Li ChenSchool of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China.
Bo-Ya CaoSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Ping HeSchool of Life Sciences, Beijing University of Chinese Medicine, Beijing, 100029, China.
Chang-Hui ZhengSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Qi-Wen LiSchool of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Wei WangSchool of Basic Medical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, 510006, China.
Jian ZhangSchool of Life Sciences, Beijing University of Chinese Medicine, Beijing, 100029, China. zhangjian@bucm.edu.cn.
Beijing University of Chinese Medicine · CNGuangzhou University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the potential molecular mechanism of tetrahydropalmatine (THP) on acute myocardial ischemia (AMI).

methodsFirst, the target genes of THP and AMI were collected from SymMap Database, Traditional Chinese Medicine Database and Analysis Platform, and Swiss Target Prediction, respectively. Then, the overlapping target genes between THP and AMI were evaluated for Grene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis and protein-protein interaction network analysis. The binding affinity between the protein and THP was assessed by molecular docking. Finally, the protective effects of THP on AMI model and oxygen and glucose deprivation (OGD) model of H9C2 cardiomyocyte were explored and the expression levels of target genes were detected by RT-qPCR in vivo and in vitro.

resultsMMP9, PPARG, PTGS2, SLC6A4, ESR1, JAK2, GSK3B, NOS2 and AR were recognized as hub genes. The KEGG enrichment analysis results revealed that the potential target genes of THP were involved in the regulation of PPAR and hormone pathways. THP improved the cardiac function, as well as alleviated myocardial cell damage. Furthermore, THP significantly decreased the RNA expression levels of MMP9, PTGS2, SLC6A4, GSK3B and ESR1 (P<0.05, P<0.01) after AMI. In vitro, THP significantly increased H9C2 cardiomyocyte viability (P<0.05, P<0.01) and inhibited the RNA expression levels of PPARG, ESR1 and AR (P<0.05, P<0.01) in OGD model.

conclusionsTHP could improve cardiac function and alleviate myocardial injury in AMI. The underlying mechanism may be inhibition of inflammation, the improvement of energy metabolism and the regulation of hormones.

Indexed as

Drugs, Chinese HerbalMyocardial IschemiaBerberine AlkaloidsCyclooxygenase 2GlucoseHumansMatrix Metalloproteinase 9Molecular Docking SimulationNetwork PharmacologyPPAR gammaRNASerotonin Plasma Membrane Transport ProteinsBerberine AlkaloidsCyclooxygenase 2Drugs, Chinese HerbalGlucoseMatrix Metalloproteinase 9PPAR gammaRNASerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, humantetrahydropalmatineacute myocardial infarctionenergy metabolismhormoneinflammationtetrahydropalmatine

Identifiers

PMID37606869
OpenAlexW4386046315

What Socratic holds

Textmetadata
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 Socratic graph.