Evidence map›Paper›PMID 35067174›Full record

ArticleBioengineered2022

Utilizing network pharmacology and experimental validation to explore the potential molecular mechanisms of BanXia-YiYiRen in treating insomnia.

Liang Wang, Peng Wang, Yingfan Chen, Chen Li, Xuelin Wang, Yin Zhang, Shaodan Li, Minghui Yang

Open access · goldAbstract readValidation StudyVideo-Audio Media
In one paragraph

Article in Bioengineered, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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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.

Liang WangChinese PLA Medical School, Beijing, People's Republic of China.
Peng WangChinese PLA Medical School, Beijing, People's Republic of China.
Yingfan ChenChinese PLA Medical School, Beijing, People's Republic of China.
Chen LiChinese PLA Medical School, Beijing, People's Republic of China.
Xuelin WangChinese PLA Medical School, Beijing, People's Republic of China.
Yin ZhangDepartment of Traditional Chinese Medicine, Chinese PLA General Hospital, Beijing, People's Republic of China.
Shaodan LiDepartment of Traditional Chinese Medicine, Chinese PLA General Hospital, Beijing, People's Republic of China.
Minghui YangDepartment of Traditional Chinese Medicine, Chinese PLA General Hospital, Beijing, People's Republic of China.
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BanXia-YiYiRen (Pinellia Ternata and Coix Seed, BX-YYR) has been clinically proven to be an effective Chinese medicine compatible with the treatment of insomnia. However, the underlying mechanism of BX-YYR against insomnia remains unclear. This study aimed to explore the pharmacological mechanisms of BX-YYR in treating insomnia based on network pharmacology and experimental validation. The drug-disease targets were obtained using publicly available databases. The analysis revealed 21 active compounds and 101 potential targets of BX-YYR from the pharmacological database of Chinese medicine system and analysis platform (TCMSP) and 1020 related targets of insomnia from the GeneCards and Online Mendelian Inheritance in Man (OMIM) databases. Furthermore, 38 common targets of BX-YYR against insomnia were identified, and these common targets were used to construct a protein-protein interaction (PPI) network. The visual PPI network was constructed by Cytoscape software. The top three genes from PPI according to degree value are FOS, AKT1, and CASP3. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment were applied to reveal the potential targets and signaling pathways involved in BX-YYR against insomnia, especially the serotonergic pathway. In addition, molecular docking revealed that baicalein, beta-sitosterol, and stigmasterol displayed strong binding to AKT1, FOS, PRKCA, and VEGFA. Experimental study found that BX-YYR against insomnia might play a role in improving sleep by modulating the serotonergic pathway. In summary, our findings revealed the underlying mechanism of BX-YYR against insomnia and provided an objective basis for further experimental study and clinical application.

Indexed as

Drugs, Chinese HerbalMolecular Docking SimulationNetwork PharmacologySleep Initiation and Maintenance DisordersAnimalsHumansMaleProtein Interaction MapsRatsRats, WistarDrugs, Chinese Herbal5-HTBanXia-YiYiRenexperimental verificationinsomniamechanism of actionmolecular dockingnetwork pharmacologyserotonergic pathway

Identifiers

PMID35067174
PMCPMC8974230
OpenAlexW4206943962

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.