Abstract | PURPOSE: METHODS: We determined the counts of Th17 and Treg cells in the serum of 15 COPD and 10 healthy subjects. Then, cigarette smoke extract-induced COPD mice were gavaged with low, middle, and high doses of XBCQ, respectively. Weight loss, pulmonary function and inflammation, Th17/Treg ratio, and gut microbiota were measured to evaluate the efficacy of XBCQ on COPD. RESULTS:
COPD patients had a higher Th17/Treg ratio in the serum than healthy controls, which was consistent with the results in the lung and colon of COPD mice. The middle dose of XBCQ (M-XBCQ) significantly decreased the weight loss and improved the pulmonary function (FEV0.2/FVC) in COPD mice. Moreover, M-XBCQ alleviated lung inflammation by rectifying the Th17/Treg imbalance, reducing the expressions of TNF-α, IL-1β, and MMP-9, and suppressing inflammatory cells infiltration. Meanwhile, M-XBCQ greatly improved the microbial homeostasis in COPD mice by accumulating probiotic Gordonibacter and Akkermansia but inhibiting the growth of pathogenic Streptococcus, which showed significant correlations with pulmonary injury. CONCLUSION: Oral M-XBCQ could alleviate COPD exacerbations by reshaping the gut microbiota and improving the Th17/Treg balance, which aids in elucidating the mechanism through which XBCQ as a therapy for COPD.
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Authors | Yongan Wang, Na Li, Qiuyi Li, Zirui Liu, Yalan Li, Jingwei Kong, Ruijuan Dong, Dongyu Ge, Jie Li, Guiying Peng |
Journal | International journal of chronic obstructive pulmonary disease
(Int J Chron Obstruct Pulmon Dis)
2021
Vol. 16
Pg. 3317-3335
ISSN: 1178-2005 [Electronic] New Zealand |
PMID | 34916790
(Publication Type: Journal Article)
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Copyright | © 2021 Wang et al. |
Chemical References |
- Drugs, Chinese Herbal
- xuanbai chengqi
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Topics |
- Animals
- Disease Models, Animal
- Drugs, Chinese Herbal
- Gastrointestinal Microbiome
- Humans
- Mice
- Pneumonia
(drug therapy, metabolism, prevention & control)
- Pulmonary Disease, Chronic Obstructive
(metabolism)
- T-Lymphocytes, Regulatory
- Th17 Cells
(metabolism)
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