Evidence map›Paper›PMID 36566207›Full record

ArticleChinese medicine2022

Integrating network pharmacology, UPLC-Q-TOF-MS and molecular docking to investigate the effect and mechanism of Chuanxiong Renshen decoction against Alzheimer's disease.

Zhuo Jun Shen, Yun Bo Fu, Jin Ling Hou, Lu Ning Lin, Xiao Yan Wang, Chang Yu Li, Yuan Xiao Yang

Open access · goldAbstract read
In one paragraph

Article in Chinese medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 23 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

7 authors at 2 institutions in 1 country.

Zhuo Jun Shen *School of Pharmacy, Hangzhou Medical College, Hangzhou, China.
Yun Bo Fu *Department of Pharmacy, Zhejiang Chinese Medical University, Hangzhou, China.
Jin Ling HouSchool of Pharmacy, Hangzhou Medical College, Hangzhou, China.
Lu Ning LinDepartment of Pharmacy, Zhejiang Chinese Medical University, Hangzhou, China.
Xiao Yan WangSchool of Pharmacy, Hangzhou Medical College, Hangzhou, China.
Chang Yu LiDepartment of Pharmacy, Zhejiang Chinese Medical University, Hangzhou, China. lcyzcmu@sina.com.
Yuan Xiao YangSchool of Basic Medical Sciences and Forensic Medicine, Hangzhou Medical College, Hangzhou, China. yyx104475@163.com.ORCID http://orcid.org/0000-0002-6182-7306
Hangzhou Medical College · CNZhejiang Chinese Medical University · CN

Funding

China Ministry of Education industry-University Cooperative Education Program 202102242039Special Funds for the Basic Research and Development Program in the Central Non-profit Research Institutesof China KYZD202006Zhejiang Province Traditional Chinese Medicine Science and Technology Project 2019ZA077Zhejiang Xinmiao Talents Program 2022R424B010
6 · The paper itself

Abstract

BACKGROUND AND

aimChuanxiong Renshen decoction (CRD) is a traditional Chinese medicine compound used to treat Alzheimer's disease (AD). However, the effects and active ingredients of CRD and its mechanism have not been clarified. We aimed to determine the neuroprotective effects of CRD in a triple-transgenic mouse model of AD (3 × Tg-AD) and investigate the possible active ingredients and their mechanisms.

methodsMorris water maze (MWM) tests were used to determine the protective effect of CRD on learning and memory ability. Afterward, we used brain tissue staining, immunofluorescent staining and western blotting to detect the neuroprotective effects of CRD. Ultraperformance liquid-chromatography-quadrupole-time-of-flight tandem mass spectrometry (UPLC-Q-TOF-MS) was applied to determine the ingredients of CRD, and the potential AD targets were obtained from DisGeNET and the GeneCards database. The protein‒protein interaction (PPI) network was built with the additional use of STRING 11.0. Metascape was used in the pathway enrichment analysis. Discovery Studio 2016 (DS) software was used to analyze the binding ability of CRD and AD-related genes. Finally, we verified the regulatory effect of CRD on the predicted core targets EGFR and CASP3 by western blotting.

resultsOur study indicated that CRD can significantly improve learning and memory, reduce the expression of Aβ and protect neurons. A total of 95 ingredients were identified in the CRD. Then, 25 ingredients were identified in serum, and 5 ingredients were identified in the brain tissue homogenate. PPI network analysis identified CASP3, EGFR, APP, CNR1, HIF1A, PTGS2 and MTOR as hub targets. KEGG and GO analyses revealed that the TNF signaling pathway and MAPK signaling pathway were enriched in multiple targets. The results of molecular docking proved that the binding of the ingredients with potential key targets was excellent. The western blotting results showed that CRD could significantly reduce the expression of CASP3 and EGFR in the hippocampus of 3 × Tg-AD mice. Combined with literature analysis, we assumed the neuroprotective effect of CRD on AD may occur through regulation of the MAPK signaling pathway.

conclusionCRD significantly alleviated injury in 3 × Tg-AD mice. The possible active ingredients are ferulic acid, rutin, ginsenoside Rg1 and panaxydol. The therapeutic effect of CRD on AD is achieved through the downregulation of CASP3 and EGFR. The neuroprotective effect of CRD on AD may occur through regulation of the MAPK signaling pathway.

Indexed as

Alzheimer's disease (AD)1Chuanxiong Renshen decoction (CRD)2Molecular docking5Network pharmacology4Ultraperformance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UPLC-Q–TOF–MS)3

Identifiers

PMID36566207
PMCPMC9789652
OpenAlexW4312203469

What OpenQuestion holds

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LicenceCC BY
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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.