Evidence map›Paper›PMID 37814868›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2023

[Exploring the therapeutic mechanism of

Q Zhang, M Zhang, Y Liu, Y Wang, F Lv, Y Wang

Open access · greenAbstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. [Protective effect ofNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Article
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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

6 authors at 1 institution in 1 country.

Q ZhangDepartment of Traditional Chinese Medicine, Sixth Medical Center, General Hospital of the Chinese People's Liberation Army, Beijing 100048, China.
M ZhangTelemedicine Unit, Medical Security Centre, General Hospital of the Chinese People's Liberation Army, Beijing 100853, China.
Y LiuDepartment of Neurology, First Medical Center, General Hospital of the Chinese People's Liberation Army, Beijing 100853, China.
Y WangDepartment of Traditional Chinese Medicine, Sixth Medical Center, General Hospital of the Chinese People's Liberation Army, Beijing 100048, China.
F LvDepartment of Traditional Chinese Medicine, Sixth Medical Center, General Hospital of the Chinese People's Liberation Army, Beijing 100048, China.
Y WangDepartment of Traditional Chinese Medicine, Sixth Medical Center, General Hospital of the Chinese People's Liberation Army, Beijing 100048, China.
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the therapeutic mechanism of

methodsTCMSP and Batman-TCM databases were searched for the active ingredients and targets of LWSZD and a herb-active ingredient-target network was constructed, and the disease targets were obtained from the OMIM, Genecards and Gene databases.The common targets were imported into STRING database and Cytoscape software to screen the core therapeutic targets, and GO enrichment and KEGG pathway analyses were performed using DAVID database.Molecular docking of the main active ingredients of LWSZD and the core targets was conducted using AutoDock, and the results were verified by observing the therapeutic effects of LWSZD and zolpidem in a rat model of PI induced by bilateral ovariectomy and intraperitoneal p-chlorophenylalanine injection.

resultsA total of 99 active ingredients, 389 drug targets, 187 PI-related targets, and 15 drug-PI common targets were screened.The core active ingredients were armepavine, sanjoinenine and mairin, and the core targets included ESR1, SIRT1, SERPINE1, COMT and CCL2, which were involved in the positive regulation of transcription from RNA polymerase II promoter, signal transduction, response to drug and positive regulation of transcription and in the pathways of dopaminergic synapses, tyrosine metabolism and tryptophan metabolism.Molecular docking results showed that LWSZD had a strong binding with ESR1, SIRT1 and SERPINE1 and was comparable to zolpidem.In the rat models of PI, treatment with LWSZD effectively alleviated the symptoms of insomnia (

conclusionThe active ingredients armepavine, sanjoinenine and mairin in LWSZD may synergistically regulate the expressions of ESR1, SIRT1 and SERPINE1 to improve PI in rats.

Indexed as

Animal ExperimentationDrugs, Chinese HerbalSleep Initiation and Maintenance DisordersAnimalsBetulinic AcidFemaleMolecular Docking SimulationNetwork PharmacologyPerimenopauseRatsSirtuin 1ZolpidemBetulinic AcidDrugs, Chinese HerbalSirtuin 1Zolpidemanimal experimentLiuwei Suanzao decoctionmolecular dockingnetwork pharmacologyperimenopausal insomnia

Identifiers

PMID37814868
PMCPMC10563099
OpenAlexW4387472546

What OpenQuestion 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 OpenQuestion graph.