# Effects of Modified Gamchogeongang-Tang on Lung Injury in a Chronic Obstructive Pulmonary Disease Mice Model: An Experimental Study

**Authors:** Won-Kyung Yang, Jin Hoo Kim, Seung-Hyung Kim, Su Won Lee, In Chul Jung, Seong-Cheon Woo, Yang Chun Park

PMC · DOI: 10.3390/ph19010187 · 2026-01-21

## TL;DR

This study shows that modified Gamchogeongang-Tang reduces lung injury and inflammation in a mouse model of COPD.

## Contribution

The study demonstrates the anti-inflammatory effects of GGS01 in a COPD mouse model through multiple experimental techniques.

## Key findings

- GGS01 reduced neutrophil levels and immune cell activity in bronchoalveolar lavage fluid and lung tissue.
- GGS01 inhibited the increase of pro-inflammatory cytokines like IL-1α, TNF-α, and IL-17A.
- Histological lung tissue damage scores and MUC5AC mRNA expression were significantly reduced by GGS01.

## Abstract

Objectives: This study evaluated the effects of modified Gamchogeongang-tang (GGS01) on lung injury using a COPD mouse model. Methods: C57BL/6 mice were exposed to cigarette smoke extract and lipopolysaccharide and treated with GGS01 (100, 200, or 400 mg/kg). Bronchoalveolar lavage fluid (BALF) and lung tissue were analyzed using cytospin, enzyme-linked immunosorbent assay, real-time polymerase chain reaction (PCR), flow cytometry analysis, hematoxylin and eosin (H&E) and Masson’s trichrome staining, and immune histology fluorescent staining. Results: GGS01 significantly inhibited the increase in neutrophils in BALF, decreased immune cell activity in BALF and lung tissue, and inhibited the increase in the levels of IL-1α, TNF-α, IL-17A, MIP2, and CXCL-1 in BALF. Conclusions: Real-time PCR analysis showed that MUC5AC mRNA expression in lung tissue significantly decreased compared with the control group. The score of histological analysis of lung tissue damage was significantly reduced, and a decrease in IRAK1 and TNF-α expression in lung tissue was observed.

## Linked entities

- **Genes:** MUC5AC (mucin 5AC, oligomeric mucus/gel-forming) [NCBI Gene 4586], IRAK1 (interleukin 1 receptor associated kinase 1) [NCBI Gene 3654], TNF (tumor necrosis factor) [NCBI Gene 7124]
- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002)

## Full-text entities

- **Genes:** Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Muc5ac (mucin 5, subtypes A and C, tracheobronchial/gastric) [NCBI Gene 17833] {aka 2210005L13Rik, MGM}, Il1a (interleukin 1 alpha) [NCBI Gene 16175] {aka Il-1a}, Irak1 (interleukin-1 receptor-associated kinase 1) [NCBI Gene 16179] {aka IRAK, IRAK-1, IRAK1-S, IRAK1b, Il1rak, Plpk}, Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Cxcl2 (C-X-C motif chemokine ligand 2) [NCBI Gene 20310] {aka CINC-2a, GROb, Gro2, MIP-2, MIP-2a, Mgsa-b}, Cxcl1 (C-X-C motif chemokine ligand 1) [NCBI Gene 14825] {aka Fsp, Gro1, KC, Mgsa, N51, Scyb1}
- **Diseases:** COPD (MESH:D029424), Lung Injury (MESH:D055370)
- **Chemicals:** lipopolysaccharide (MESH:D008070), GGS01 (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12844599/full.md

---
Source: https://tomesphere.com/paper/PMC12844599