Evidence map›Paper›PMID 37089711›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2023

Pharmacodynamic Material Basis and Potential Mechanism Study of Spatholobi Caulis in Reversing Osteoporosis.

Jianpeng Xiao, Wei Shang, Zhiming Zhao, Jun Jiang, Jianping Chen, Hui Cai, Jinjin He, Zhihui Cai, Zihan Zhao

Open access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-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

3 citing papers in PubMed, 10 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

9 authors at 3 institutions in 2 countries.

Jianpeng XiaoDepartment of TCM, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, China.ORCID https://orcid.org/0000-0002-3267-9746
Wei ShangDepartment of TCM, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, China.
Zhiming ZhaoDepartment of TCM, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, China.
Jun JiangDepartment of TCM, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, China.ORCID https://orcid.org/0000-0002-6342-165X
Jianping ChenSchool of Chinese Medicine, The University of Hong Kong, 10 Sassoon Road, Pokfulam, Hong Kong, China.ORCID https://orcid.org/0000-0001-6494-5271
Hui CaiDepartment of TCM, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, China.ORCID https://orcid.org/0000-0002-1146-8747
Jinjin HeSchool of Pharmacy, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, Jiangsu, China.ORCID https://orcid.org/0000-0002-6532-3295
Zhihui CaiSchool of Pharmacy, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, Jiangsu, China.
Zihan ZhaoSchool of Pharmacy, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, Jiangsu, China.
Jiangsu University · CNNanjing General Hospital of Nanjing Military Command · CNUniversity of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To elucidate the mechanism of Spatholobi Caulis (SC) in treating osteoporosis (OP) integrated zebrafish model and bioinformatics. Methods: Skeleton staining coupled with image quantification was performed to evaluate the effects of SC on skeleton mineralization area (SSA) and total optical density (TOD). Zebrafish locomotor activity was monitored using the EthoVision XT. Bioactive compounds of SC and their corresponding protein targets were acquired from Traditional Chinese Medicine Systems Pharmacology (TCMSP) database. Potential therapeutic targets for OP were summarized through retrieving 5 databases, and then, the overlapping genes between SC and OP were acquired. The core genes were selected by CytoHubba. Subsequently, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway and Gene Ontology (GO) functional analysis of the intersection target genes were carried out by R software. Finally, the molecular docking simulation was manipulated between the ingredients and the hub genes. Results: Compared with the model group, SC significantly increased the SSA and TOD at 10 mg/mL and improved the locomotor activity in a dose-dependent manner ( Conclusion: SC had the hierarchical network characteristics of "multicomponents/multitargets/multifunctions/multipathways" in reversing OP, but AGE-RAGE signaling pathway may be the main regulatory mechanism.

Identifiers

PMID37089711
PMCPMC10121353
OpenAlexW4365504353

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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.