Evidence map›Paper›PMID 40598199›Full record

ArticleChinese medicine2025

Multi-omics and network pharmacology reveal Huayu-Tongbi decoction reduced arthritis-related bone erosion.

Bozhen Chen, Lu Yang, Houchun Wang, Peng Yu, Mengyang Ma, Meiqi Chen, Yingyan Zhou, Jiaqi Wu, Huasheng Liang, Maojie Wang and 4 more

Abstract read
In one paragraph

Article in Chinese medicine, 2025. 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. Review
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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

14 authors.

Bozhen Chen *Second Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Lu Yang *Second Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Houchun WangSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Peng YuSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Mengyang MaSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Meiqi ChenSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Yingyan ZhouSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Jiaqi WuSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Huasheng LiangSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Maojie WangSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Runyue HuangSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Yiting HeSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Qingchun HuangSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China.
Xiaohong HeSecond Clinical Medical College of Guangzhou University of Chinese Medicine, No.111, Dade Road, Yuexiu District, Guangzhou City, 510120, Guangdong, People's Republic of China. wdtsxh521@126.com.ORCID http://orcid.org/0000-0002-3921-1564

Funding

Guangdong Basic and Applied Basic Research Foundation 2020B1515130005Guangdong Provincial Hospital of Chinese Medicine YN2023MB15Guangdong Provincial Hospital of Chinese Medicine YN2024GZRPY027Guangdong Provincial Key laboratory of Chinese Medicine for Prevention and Treatment of Refractory Chronic Diseases 2023KT15525Guangzhou Science and Technology Planing Project 2024A04J3382Guangzhou Science and Technology Planing Project No.2025A03J4076National Natural Science Foundation of China 82174285Natural Science Foundation of Guangdong Province No. 2024A1515012464
6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA), an autoimmune disorder marked by joint inflammation and bone destruction, lacks effective therapies targeting bone erosion. Huayu-Tongbi decoction (HT), a traditional Chinese medicine (TCM) herbal decoction, has been used as a complementary treatment for RA, yet the mechanisms of its active components and multitarget therapeutic effects remain unclear. MATERIALS AND

methodsAn adjuvant-induced arthritis (AIA) model was established in rats, and enzyme-linked immunosorbent assay, histopathological staining, and micro-Computed Tomography to assess the effects of HT on joint inflammation and bone erosion. Furthermore, serum pharmacochemistry combined with network pharmacology identified the HT's active ingredients and targets. In vitro multi-omics study revealed the decoction's effect and underlying mechanisms in osteoclastic differentiation.

resultsHT significantly reduced joint inflammation and bone erosion in AIA rats. Serum pharmacochemistry identified 44 absorbed components in HT, and network pharmacology analysis predicted 89 key targets of HT related to RA. In vitro experiments demonstrated that HT inhibited RANKL-induced osteoclastic differentiation through multiple pathways, such as PPAR pathway, AA metabolism, and NF-κB pathway.

conclusionThis study confirmed the beneficial effects of HT in experimental arthritis and explored the specific mechanisms involved. HT inhibited osteoclastic differentiation through multiple targets and pathways to reduced bone destructions, providing a potential therapeutic strategy for preventing RA-related bone erosion.

Indexed as

Bone erosionHuayu-Tongbi decoctionMultiomicsNetwork pharmacologyRheumatoid arthritisTraditional Chinese Medicine

Identifiers

PMID40598199
PMCPMC12220612

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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.