# Unveiling the pathways of Xuanbai Chengqi Decoction in obese asthma: from immune modulation to microbial restoration

**Authors:** Ke Lu, Chen Li, Qingxiang Zhang, HongXiang Li, Chen Ding, Lu Zhang, Feng Cao

PMC · DOI: 10.3389/fnut.2026.1710739 · Frontiers in Nutrition · 2026-01-23

## TL;DR

This study explores how Xuanbai Chengqi Decoction treats obese asthma by balancing immune responses and restoring gut microbes.

## Contribution

The study reveals a novel mechanism of XBCQD in treating obese asthma through immune modulation and microbial restoration.

## Key findings

- XBCQD reduces lung inflammation and serum IgE levels in obese asthmatic mice.
- XBCQD restores beneficial gut bacteria and increases short-chain fatty acids in the intestines.
- XBCQD regulates Th17/Treg immune imbalance via the SCFAs/GPR43/NLRP3 pathway.

## Abstract

Obesity asthma is a unique asthma phenotype, which has the characteristics of aggravation of clinical symptoms, change of immune response, and resistance to standard treatment. Obese asthma, as a clinical refractory asthma type, urgently needs effective and side-effect-free treatment. Xuanbai Chengqi Decoction (XBCQD) is a traditional Chinese medicine prescription widely used in the treatment of lung diseases, including asthma in China. However, the efficacy and mechanism of obese asthma remain to be explored.

To elucidate the therapeutic effect of XBCQD on obese asthma and reveal its mechanism.

Network pharmacology was used to predict the potential therapeutic targets and pathways of XBCQD in the treatment of obese asthma. We established a mouse model of obese asthma by feeding a high-fat diet combined with intraperitoneal injection of ovalbumin (OVA) to induce sensitization, and then intervened with intragastric administration of high, medium, and low doses of XBCQD. During the modeling period, lung function and body weight of mice were used to evaluate the preparation of the obese asthma model. H&E staining, RT-qPCR, ELISA, Western blot, and flow cytometry were used to quantify Th cell subsets, 16S rRNA sequencing was used to determine microbial composition, and GC/MS was used to detect the content of short-chain fatty acids in intestinal contents to explore the mechanism of Xuanbai Chengqi Decoction on obese asthma.

Network pharmacology showed that XBCQD may improve obese asthma by affecting core targets such as IL-6, TNF, and Caspase1, and through signaling pathways such as the IL-17 signaling pathway, AGE-RAGE signaling pathway, TNF signaling pathway, and Th17 cell differentiation. Experimental studies have found that XBCQD can alleviate the symptoms of obese asthma and lung inflammation, reduce serum IgE, reduce the expression of IL-6, IL-17, and IL-23 in serum, to reduce lung inflammation induced by obese asthma in mice; flow cytometry of spleen tissue showed that XBCQD reduced the proportion of Th17 cells and restored the proportion of Treg cells. Proteomics showed that XBCQD inhibited the expression of NLRP3, Caspase-1, and IL-1β by up-regulating the expression of GPR43, thereby inhibiting Th17-related protein RORγt and restoring Treg-related protein Foxp3, thereby regulating immune imbalance. At the same time, XBCQD restored the intestinal microbial species, and restored the beneficial bacteria such as Dubosiella, Akkermansia_muciniphila, Rikenella, which were reduced in obese asthmatic mice, and increased the content of acetic acid, propionic acid, and butyric acid in intestinal flora metabolites.

XBCQD regulates Th17/Treg immune imbalance in obese asthma by improving intestinal microecology and regulating SCFAs/GPR43/NLRP3 pathway. These findings provide new pharmacological evidence for its clinical application in obese asthma.

Diagram illustrating a study on the effects of Xuanbai Chengqi decoction on obese asthma. It consists of four panels: network pharmacology prediction, experimental procedure, results, and conclusion. The first panel shows Venn diagrams, networks, and graphs of medicinal compounds. The second outlines the experimental process with herbs and test subjects. The third details results, including lab equipment, graphs, and effects on asthma symptoms and cellular pathways. The fourth concludes with diagrams depicting biological processes influenced by the treatment, emphasizing cellular and microbial changes.

## Linked entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569], TNF (tumor necrosis factor) [NCBI Gene 7124], Caspase1 (caspase-1) [NCBI Gene 692604], IL17A (interleukin 17A) [NCBI Gene 3605], IL37 (interleukin 37) [NCBI Gene 27178], IL1B (interleukin 1 beta) [NCBI Gene 3553], NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548], Caspase1 (caspase-1) [NCBI Gene 692604], FFAR2 (free fatty acid receptor 2) [NCBI Gene 2867], FOXP3 (forkhead box P3) [NCBI Gene 50943]
- **Diseases:** asthma (MONDO:0004979)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Renbp (renin binding protein) [NCBI Gene 19703] {aka Age, Rnbp}, Foxp3 (forkhead box P3) [NCBI Gene 20371] {aka JM2, scurfin, sf}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Ffar2 (free fatty acid receptor 2) [NCBI Gene 233079] {aka GPCR43, Gpr43}, Il23a (interleukin 23, alpha subunit p19) [NCBI Gene 83430] {aka IL-23, p19}, Nlrp3 (NLR family, pyrin domain containing 3) [NCBI Gene 216799] {aka AGTAVPRL, AII/AVP, Cias1, FCAS, FCU, MWS}, Casp1 (caspase 1) [NCBI Gene 12362] {aka ICE, Il1bc}, Ager (advanced glycosylation end product-specific receptor) [NCBI Gene 11596] {aka RAGE}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Serpinb1-ps1 (serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene) [NCBI Gene 282665] {aka EID, ovalbumin}
- **Diseases:** lung diseases (MESH:D008171), lung inflammation (MESH:D011014), asthmatic (MESH:D013224), asthma (MESH:D001249), Obese asthma (MESH:D009765)
- **Chemicals:** acetic acid (MESH:D019342), H&amp;E (MESH:D006371), butyric acid (MESH:D020148), SCFAs (MESH:D005232), propionic acid (MESH:C029658)
- **Species:** Akkermansia muciniphila (species) [taxon 239935], Rikenella (genus) [taxon 28138], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12875951/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC12875951/full.md

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Source: https://tomesphere.com/paper/PMC12875951