# Multi-Targeted Therapeutic Mechanisms of Huangqi Guizhi Wuwu Decoction Against Rheumatoid Arthritis: An Integrated Approach Combining Serum Pharmacochemistry, Network Pharmacology, Metabolomics, and Experimental Validation

**Authors:** Zihua Xu, Zhenshu Li, Jiameng Qu, Chen Liang, Yingshi Zhang, Qingchun Zhao, Qing Li

PMC · DOI: 10.3390/ph19020236 · Pharmaceuticals · 2026-01-29

## TL;DR

This study explores how a traditional Chinese medicine formula treats rheumatoid arthritis by identifying its active components and mechanisms through multiple scientific methods.

## Contribution

The study identifies key active components and their multi-target mechanisms in a traditional Chinese medicine formula for rheumatoid arthritis.

## Key findings

- HGWD contains 25 absorbed compounds that target TNF, IL-17, and MAPK pathways.
- HGWD reduces joint inflammation and pro-inflammatory cytokines in arthritis rats.
- Four active components show anti-inflammatory effects comparable to the full extract.

## Abstract

Background: The pathogenesis of rheumatoid arthritis (RA) is closely related to multiple disorders in the immune and metabolic systems, which indicates that a multi-target therapy strategy may have advantages over traditional single-target therapy. Huangqi Guizhi Wuwu Decoction (HGWD), as a classic traditional Chinese medicine formula that has been used to treat RA in clinic, is a potential source of multi-target natural medicine. However, its active components and mechanism of action still need further research. Methods: This study combined serum pharmacochemistry, non-targeted metabonomics, network pharmacology, and experimental verification and comprehensively analyzed the therapeutic mechanism and pharmacodynamic basis of HGWD. Results: Through HPLC-Q-TOF-MS/MS, a total of 99 chemical components were identified. Among them, 25 prototype compounds were absorbed into the systemic circulation. The study of network pharmacology indicates that these compounds are concentrated in TNF, IL-17, and MAPK signaling pathways. In collagen-induced arthritis rats, HGWD can effectively alleviate joint inflammation, inhibit the production of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6, IL-17), block the activation of the MAPK pathway, and restore 13 abnormal metabolic markers related to lipid and amino acid metabolism. In addition, the researchers identified and verified the combination of four active components (calycosin, paeoniflorin, 6-gingerol, and formononetin) in vitro, and its anti-inflammatory and anti-migration activities were equivalent to or stronger than those of the complete extract. Pharmacokinetic analysis also confirmed that these components were fully exposed in vivo. Conclusions: These findings reveal the mechanism of multi-component therapy of HGWD and identify the potential bioactive components, which can be used to develop multi-target therapeutic drugs for RA based on natural products.

## Linked entities

- **Chemicals:** calycosin (PubChem CID 5280448), paeoniflorin (PubChem CID 442534), 6-gingerol (PubChem CID 3473), formononetin (PubChem CID 5280378), IL-6 (PubChem CID 165368475)
- **Diseases:** rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Genes:** Lox (lysyl oxidase) [NCBI Gene 24914] {aka H-rev142, Rrg1}, Cpox (coproporphyrinogen oxidase) [NCBI Gene 304024], MAPK3 (mitogen-activated protein kinase 3) [NCBI Gene 5595] {aka ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1}, Cd4 (Cd4 molecule) [NCBI Gene 24932] {aka W3/25, p55}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 83785] {aka VEGF-A, VEGF111, VEGF164, VPF, Vegf}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, Trav12-3 (T cell receptor alpha variable 12-3) [NCBI Gene 691058] {aka RGD1564212}, Il17a (interleukin 17A) [NCBI Gene 301289] {aka CTLA-8, IL-17, IL-17A, Il17}, Jun (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 24516], Mapk14 (mitogen activated protein kinase 14) [NCBI Gene 81649] {aka CRK1, CSBP, CSPB1, Csbp1, Csbp2, Exip}, Il6 (interleukin 6) [NCBI Gene 24498] {aka ILg6, Ifnb2}, TNF (tumor necrosis factor) [NCBI Gene 280943] {aka TNF-a, TNF-alpha, TNFa}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Mapk8 (mitogen-activated protein kinase 8) [NCBI Gene 116554] {aka JNK}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, Il1b (interleukin 1 beta) [NCBI Gene 24494] {aka IL-1F2}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}, JUN (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3725] {aka AP-1, AP1, c-Jun, cJUN, p39}, Crp (C-reactive protein) [NCBI Gene 25419] {aka Aa1249, Ab1-341, Ab2-196, Ac1-114, Ac1262, Ac2-069}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** tuberculosis (MESH:D014376), peripheral neuropathy (MESH:D010523), inflammatory cytokines (MESH:D000080424), motor dysfunction (MESH:D000068079), erythema (MESH:D004890), synovial hyperplasia (MESH:D006965), MS (MESH:D009103), joint destruction (MESH:D008105), immune dysregulation (OMIM:614878), joint deformation (MESH:D016916), RA (MESH:D001172), Arthritis (MESH:D001168), toxicity (MESH:D064420), rheumatoid factor (MESH:D001171), joint pain (MESH:D018771), bone (MESH:D001847), synovitis (MESH:D013585), infections (MESH:D007239), ankle swelling (MESH:D016512), autoimmune disease (MESH:D001327), weight gain (MESH:D015430), pannus (MESH:C537858), cartilage (MESH:D002357), metabolic abnormalities (MESH:D008659), arthritic (MESH:D015535), pain (MESH:D010146), metabolic disturbances (MESH:D024821), Inflammatory (MESH:D007249), injury to (MESH:D014947), hepatitis C (MESH:D019698), hepatitis B (MESH:D006509), swelling (MESH:D004487), cardiopulmonary complications (MESH:D006323)
- **Chemicals:** nucleosides (MESH:D009705), IS (MESH:D007455), paraformaldehyde (MESH:C003043), lipid (MESH:D008055), albiflorin (MESH:C014959), LPS (MESH:D008070), 6-methylcoumarin (MESH:C018096), citrate (MESH:D019343), CO2 (MESH:D002245), protocatechuic acid (MESH:C009091), flavonoids (MESH:D005419), DMSO (MESH:D004121), heparin sodium (MESH:D006493), PVDF (MESH:C024865), L-tryptophan (MESH:D014364), PBS (MESH:D007854), eosin (MESH:D004801), hematoxylin (MESH:D006416), 2-methylcitrate (MESH:C031605), penicillin (MESH:D010406), sulfanilamide (MESH:D000077145), H&amp;E (MESH:D006371), crystal violet (MESH:D005840), eicosanoids (MESH:D015777), hippurate (MESH:C030514), 4-aminobutanoate (-), arginine (MESH:D001120), monoterpenes (MESH:D039821), phenylalanine (MESH:D010649), phenols (MESH:D010636), triterpenoids (MESH:D014315), MTT (MESH:C070243), amino acid (MESH:D000596), phosphoric acid (MESH:C030242), geniposide (MESH:C007835), leukotrienes (MESH:D015289), cinnamic acid (MESH:C029010), Paeoniflorin (MESH:C015423), arachidonic acid (MESH:D016718), isoflurane (MESH:D007530), Griess reagent (MESH:C095000), 6-Gingerol (MESH:C007845), Formononetin (MESH:C007768), D-gluconic acid (MESH:C030691), MTX (MESH:D008727), water (MESH:D014867), azelaic acid (MESH:C010038), 6-shogaol (MESH:C040115), NO (MESH:D009569), ethanol (MESH:D000431), glutamate (MESH:D018698), N-(1-naphthyl) ethylenediamine dihydrochloride (MESH:C008588), N-acetyl-L-glutamate (MESH:C016195), kynurenine (MESH:D007737), SDS (MESH:D012967), alkaloids (MESH:D000470), acetic acid (MESH:D019342), phenylacetylglycine (MESH:C022050), P (MESH:D010758), sugars (MESH:D000073893)
- **Species:** Bos taurus (bovine, species) [taxon 9913], gut metagenome (species) [taxon 749906], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Astragalus membranaceus (species) [taxon 649199], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** P0010S
- **Cell lines:** MH7A — Homo sapiens (Human), Transformed cell line (CVCL_0427), RAW264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943270/full.md

## References

82 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943270/full.md

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Source: https://tomesphere.com/paper/PMC12943270