Evidence map›Paper›PMID 37674371›Full record

ArticlePharmaceutical biology2023

Mechanism investigation of Duhuo Jisheng pill against rheumatoid arthritis based on a strategy for the integration of network pharmacology, molecular docking and

Ping Xin, Xiaoyun Xu, Huaxi Zhang, Yuezhou Hu, Chengjie Deng, Shiqin Sun, Shuang Liu, Xuegang Zhou, Hongxing Ma, Xiaoliang Li

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 5 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

10 authors at 4 institutions in 1 country.

Ping XinCollege of Pharmacy, Harbin Medical University, Daqing, PR China.
Xiaoyun XuCollege of Pharmacy, Harbin Medical University, Daqing, PR China.
Huaxi ZhangCollege of Pharmacy, Harbin Medical University, Daqing, PR China.
Yuezhou HuCollege of Pharmacy, Harbin Medical University, Daqing, PR China.
Chengjie DengCollege of Pharmacy, Harbin Medical University, Daqing, PR China.
Shiqin SunScience and Education Department, Nanjing Lishui People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, Nanjing, PR China.
Shuang LiuCollege of Pharmacy, Harbin Medical University, Daqing, PR China.
Xuegang ZhouCollege of Pharmacy, Harbin Medical University, Daqing, PR China.
Hongxing MaClinical Laboratory Department, Nanjing Lishui People's Hospital, Zhongda Hospital Lishui Branch, Southeast University, Nanjing, PR China.
Xiaoliang LiKey Laboratory of Tropical Translational Medicine of Ministry of Education, Hainan Provincial Key Laboratory for Research and Development of Tropical Herbs, Haikou Key Laboratory of Li Nationality Medicine, School of Pharmacy, Hainan Medical University, Haikou, PR China.
Harbin Medical University · CNHainan Medical University · CNLishui City People's Hospital · CNSoutheast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextDuhuo Jisheng pill (DHJS) is a classic traditional Chinese medicine (TCM) formula for rheumatoid arthritis (RA). The effective components and therapeutic mechanisms of DHJS for treating RA are still unclear.

objectiveTo explore the potential mechanism of DHJS against RA by means of network pharmacology and experimental verification. MATERIALS AND

methodsA network pharmacology and molecular docking analysis based on phytochemistry was used to elucidate the mechanism of DHJS against RA. The targets of DHJS anti-RA active ingredient were obtained by searching TCMSP, ETCM and TCMSID. The RA model induced by collagen was established in Wistar rats. The rats in the DHJS group were administered doses of 0.5, 1.0 and 2.0 g/kg for a period of 10 d. The expression of targets was measured with Western blot.

resultsNetwork pharmacology analysis showed that the anti-RA effect of DHJS was mediated by targets involved in immunity, inflammation and apoptosis, as well as PI3K-Akt and NF-κB signalling pathways. Of 2.0 g/kg DHJS significantly alleviated the ankle inflammation (IL-6: 62.73 ± 8.39 pg/mL, IL-1β: 50.49 ± 11.47 pg/mL, TNF-α: 16.88 ± 3.05 pg/mL, IL-17A: 12.55 ± 1.87 pg/mL, IL-10: 16.24 ± 3.00 pg/mL), comparing with the model group (IL-6: 92.02 ± 13.25 pg/mL, IL-1β: 71.85 ± 4.12 pg/mL, TNF-α: 25.64 ± 3.69 pg/mL, IL-17A: 22.14 ± 4.56 pg/mL, IL-10: 9.51 ± 3.03 pg/mL) (

conclusionsDHJS could alleviate the collagen-induced arthritis (CIA) by the PI3K/AKT/NF-κB signalling pathway.

Indexed as

Arthritis, RheumatoidNF-kappa BAnimalsDrugs, Chinese HerbalInflammationInterleukin-10Interleukin-17Interleukin-6Molecular Docking SimulationNetwork PharmacologyPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRatsRats, WistarTumor Necrosis Factor-alphaDrugs, Chinese Herbalduhuo jishengInterleukin-10Interleukin-17Interleukin-6NF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTumor Necrosis Factor-alphabioinformation technologymolecular mechanismPI3K/AKT/NF-κB pathwayTraditional Chinese medicine

Identifiers

PMID37674371
PMCPMC10486301
OpenAlexW4386505452

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.