Evidence map›Paper›PMID 37350000›Full record

ArticleCombinatorial chemistry & high throughput screening2024

Study of Active Phytochemicals and Mechanisms of Cnidii Fructus in Treating Osteoporosis Based on HPLC-Q-TOF-MS/MS and Network Pharmacology.

Yincong Xu, Shuai Zhang, Shinong Yuan, Yanlei Su, Yuqian Jia, Yajing Zhang, Xuhong Duan

Abstract read
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In one paragraph

Article in Combinatorial chemistry & high throughput screening, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Review
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

7 authors at 6 institutions in 1 country.

Yincong XuDepartment of Ophthalmology, The First Hospital of Hebei Medical University, Shijiazhuang, 050200, China.
Shuai ZhangDepartment of Ophthalmology, The First Hospital of Hebei Medical University, Shijiazhuang, 050200, China.
Shinong YuanCollege of Pharmacy, Hebei University of Chinese Medicine, Shijiazhuang, 050200, P.R. China.
Yanlei SuBethune Internation Peace Hospital (The 980st Hospital of the PLA Joint Logistics Support Force), Shijiazhuang, 050082, P.R. China.
Yuqian JiaCollege of Pharmacy, Hebei University of Chinese Medicine, Shijiazhuang, 050200, P.R. China.
Yajing ZhangCollege of Pharmacy, Hebei University of Chinese Medicine, Shijiazhuang, 050200, P.R. China.
Xuhong DuanCollege of Pharmacy, Hebei University of Chinese Medicine, Shijiazhuang, 050200, P.R. China.
Hebei University of Chinese Medicine · CNBethune International Peace Hospital · CNFirst Affiliated Hospital of Hebei Medical University · CNHebei Medical University · CNHebei Science and Technology Department · CNHospital of Hebei Province · CN

Funding

basic scientific research business cost project of provincial universities in 2022 JCYJ2022001, JCYJ2022002Hebei administration of traditional Chinese Medicine 2022099, 2023120Science and Technology Project of Hebei Education Department BJK2023098
6 · The paper itself

Abstract

introductionThis study aimed to clarify the anti-osteoporosis mechanism of Cnidii Fructus (CF) via network pharmacology and experimental verification.

methodsHPLC fingerprints combined with HPLC-Q-TOF-MS/MS analysis confirmed common components (CC

resultsIn this study, 17 compounds from CF were identified by HPLC-Q-TOF-MS/MS and HPLC fingerprints and then were further screened key compounds and potential targets by PPI analysis, ingredient-target network and hub network. The key compounds were SCZ10 (Diosmin), SCZ16 (Pabulenol), SCZ6 (Osthenol), SCZ8 (Bergaptol) and SCZ4 (Xanthotoxol). The potential targets were SRC, MAPK1, PIK3CA, AKT1 and HSP90AA1. Molecular docking further analysis indicated that the five key compounds have a good binding affinity with related proteins. CCK8 assays, TRAP staining experiments, and ALP activity assays concluded that osthenol and bergaptol inhibited osteoclast formation and promoted osteoblast bone formation to improve osteoporosis.

conclusionBased on network pharmacology and in vitro experiments analysis, this study revealed that CF possessed an anti-OP effect, and its potential therapeutic effect may be involved with osthenol and bergaptol from CF.

Indexed as

Drugs, Chinese HerbalMolecular Docking SimulationNetwork PharmacologyOsteoporosisPhytochemicalsTandem Mass SpectrometryAnimalsChromatography, High Pressure LiquidFruitHumansMiceDrugs, Chinese HerbalPhytochemicalsCnidii fructusHPLC fingerprintsHPLC-Q-TOF-MS/MSin vitro experiments.network pharmacologyosteoporosis

Identifiers

PMID37350000
OpenAlexW4381716661

What OpenQuestion holds

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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.