Bufei Huoxue capsule attenuates COPD-related inflammation and regulates intestinal microflora, metabolites
Background: Bufei Huoxue capsule (BFHX) is widely used for the clinical treatment of chronic obstructive pulmonary disease (COPD) in China.Objectives: The aim of this study is to explore the effects on COPD and the underlying mechanism of BFHX.The process and methods: In this study, we established a COPD mouse model through cigarette smoke (CS) exposure in combination with lipopolysaccharide (LPS) intratracheal instillation. Subsequently, BFHX was orally administrated to COPD mice, and their pulmonary function, lung pathology, and lung inflammation, including bronchoalveolar lavage fluid (BALF) cell count and classification and cytokines, were analyzed. In addition, the anti-oxidative stress ability of BFHX was detected by Western blotting, and the bacterial diversity, abundance, and fecal microbiome were examined using 16S rRNA sequencing technology.Outcome: BFHX was shown to improve pulmonary function, suppress lung inflammation, decrease emphysema, and increase anti-oxidative stress, whereas 16S rRNA sequencing indicated that BFHX can dynamically regulate the diversity, composition, and distribution of the intestinal flora microbiome and regulate the lysine degradation and phenylalanine metabolism of COPD mice. These results highlight another treatment option for COPD and provide insights into the mechanism of BFHX..
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:15 |
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| Enthalten in: |
Frontiers in Pharmacology - 15(2024) |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Yuanyuan Li [VerfasserIn] |
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| Links: |
doi.org [kostenfrei] |
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| Themen: |
Bufei Huoxue capsule |
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| doi: |
10.3389/fphar.2024.1270661 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
DOAJ091509823 |
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| 520 | |a Background: Bufei Huoxue capsule (BFHX) is widely used for the clinical treatment of chronic obstructive pulmonary disease (COPD) in China.Objectives: The aim of this study is to explore the effects on COPD and the underlying mechanism of BFHX.The process and methods: In this study, we established a COPD mouse model through cigarette smoke (CS) exposure in combination with lipopolysaccharide (LPS) intratracheal instillation. Subsequently, BFHX was orally administrated to COPD mice, and their pulmonary function, lung pathology, and lung inflammation, including bronchoalveolar lavage fluid (BALF) cell count and classification and cytokines, were analyzed. In addition, the anti-oxidative stress ability of BFHX was detected by Western blotting, and the bacterial diversity, abundance, and fecal microbiome were examined using 16S rRNA sequencing technology.Outcome: BFHX was shown to improve pulmonary function, suppress lung inflammation, decrease emphysema, and increase anti-oxidative stress, whereas 16S rRNA sequencing indicated that BFHX can dynamically regulate the diversity, composition, and distribution of the intestinal flora microbiome and regulate the lysine degradation and phenylalanine metabolism of COPD mice. These results highlight another treatment option for COPD and provide insights into the mechanism of BFHX. | ||
| 650 | 4 | |a Bufei Huoxue capsule | |
| 650 | 4 | |a chronic obstructive pulmonary disease | |
| 650 | 4 | |a inflammation | |
| 650 | 4 | |a intestinal flora | |
| 650 | 4 | |a metabolites | |
| 653 | 0 | |a Therapeutics. Pharmacology | |
| 700 | 0 | |a Jiali Chen |e verfasserin |4 aut | |
| 700 | 0 | |a Yue Xing |e verfasserin |4 aut | |
| 700 | 0 | |a Jian Wang |e verfasserin |4 aut | |
| 700 | 0 | |a Qiuling Liang |e verfasserin |4 aut | |
| 700 | 0 | |a Jiamin Zeng |e verfasserin |4 aut | |
| 700 | 0 | |a Siyi Wang |e verfasserin |4 aut | |
| 700 | 0 | |a Qiong Yang |e verfasserin |4 aut | |
| 700 | 0 | |a Jianing Lu |e verfasserin |4 aut | |
| 700 | 0 | |a Jieying Hu |e verfasserin |4 aut | |
| 700 | 0 | |a Wenju Lu |e verfasserin |4 aut | |
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