A chinese herbal formula ameliorates COPD by inhibiting the inflammatory response via downregulation of p65, JNK, and p38
- Publisher:
- Elsevier
- Publication Type:
- Journal Article
- Citation:
- Phytomedicine, 2021, 83, pp. 153475
- Issue Date:
- 2021-01-20
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Li, J | |
dc.contributor.author | Xie, Y | |
dc.contributor.author | Zhao, P | |
dc.contributor.author | Qin, Y | |
dc.contributor.author | Oliver, BG | |
dc.contributor.author | Tian, Y | |
dc.contributor.author | Li, S | |
dc.contributor.author | Wang, M | |
dc.contributor.author | Liu, X | |
dc.date.accessioned | 2021-09-25T22:07:45Z | |
dc.date.available | 2021-01-17 | |
dc.date.available | 2021-09-25T22:07:45Z | |
dc.date.issued | 2021-01-20 | |
dc.identifier.citation | Phytomedicine, 2021, 83, pp. 153475 | |
dc.identifier.issn | 0944-7113 | |
dc.identifier.issn | 1618-095X | |
dc.identifier.uri | http://hdl.handle.net/10453/150702 | |
dc.description.abstract | Background Bufei Yishen formula (BYF), a traditional Chinese medicine (TCM), is an effective therapeutic strategy for patients with chronic obstructive pulmonary disease (COPD). Purpose To evaluate the efficacy of BYF and investigate its therapeutic mechanisms. Methods A total of 134 patients completed the study: 68 patients treated by BYF combined with conventional Western medicine in the trial group; and 66 patients treated using conventional Western medicine in the control group. The efficacy of BYF was evaluated by a subgroup analysis of data obtained from a four-center, open-label, randomized controlled trial of comprehensive TCM interventions. A rat model of COPD was treated with the key active molecules (KAM) of BYF for 8 weeks. An in vitro model of COPD was also treated with KAM. Results Patients treated with BYF had reduced frequency of acute exacerbation of COPD (p < 0.001) and duration (p = 0.028), dyspnea scale (p = 0.007), 6-min walking distance (p = 0.048). There were no differences observed in forced vital capacity in one second (FVC), forced expiratory volume in one second (FEV1), and FEV1 percentage of the predicted value (FEV1%). The five KAM of BYF (KAM-BYF) improved lung function, including tidal volume, minute ventilation, peak expiratory flow, FVC, FEV0.1, and FEV0.3, and pathological changes in COPD rats. Treatment with KAM-BYF markedly decreased the levels of interleukin 6 (IL6), tumor necrosis factor-α (TNF-α), matrix metalloproteinase 9 (MMP9), and MMP12 in serum and bronchial alveolar lavage fluid. In airway epithelial cells, KAM-BYF decreased the levels of TNF-α-induced IL8 and IL6. Finally, we discovered that the anti-inflammatory effects of KAM-BYF in COPD rats and BEAS-2Bs were mediated through inhibition of nuclear factor-kappaB (NF-κB) p65, c-Jun NH2-terminal kinase (JNK), and p38 mitogen-activated protein kinase signaling. Conclusions BYF exerts beneficial effects in patients with COPD via inhibition of inflammation. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | Elsevier | |
dc.relation.ispartof | Phytomedicine | |
dc.relation.isbasedon | 10.1016/j.phymed.2021.153475 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 0607 Plant Biology, 1104 Complementary and Alternative Medicine, 1115 Pharmacology and Pharmaceutical Sciences | |
dc.subject.classification | Medicinal & Biomolecular Chemistry | |
dc.subject.mesh | Bronchoalveolar Lavage Fluid | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Rats, Sprague-Dawley | |
dc.subject.mesh | Pulmonary Disease, Chronic Obstructive | |
dc.subject.mesh | MAP Kinase Kinase 4 | |
dc.subject.mesh | p38 Mitogen-Activated Protein Kinases | |
dc.subject.mesh | Tumor Necrosis Factor-alpha | |
dc.subject.mesh | NF-kappa B | |
dc.subject.mesh | Drugs, Chinese Herbal | |
dc.subject.mesh | Treatment Outcome | |
dc.subject.mesh | Down-Regulation | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Female | |
dc.subject.mesh | Male | |
dc.subject.mesh | Aged | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Bronchoalveolar Lavage Fluid | |
dc.subject.mesh | Down-Regulation | |
dc.subject.mesh | Drugs, Chinese Herbal | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | MAP Kinase Kinase 4 | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | NF-kappa B | |
dc.subject.mesh | Pulmonary Disease, Chronic Obstructive | |
dc.subject.mesh | Rats, Sprague-Dawley | |
dc.subject.mesh | Treatment Outcome | |
dc.subject.mesh | Tumor Necrosis Factor-alpha | |
dc.subject.mesh | p38 Mitogen-Activated Protein Kinases | |
dc.title | A chinese herbal formula ameliorates COPD by inhibiting the inflammatory response via downregulation of p65, JNK, and p38 | |
dc.type | Journal Article | |
utslib.citation.volume | 83 | |
utslib.location.activity | Germany | |
utslib.for | 0607 Plant Biology | |
utslib.for | 1104 Complementary and Alternative Medicine | |
utslib.for | 1115 Pharmacology and Pharmaceutical Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Strength - CHT - Health Technologies | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Life Sciences | |
pubs.organisational-group | /University of Technology Sydney/Centre for Health Technologies (CHT) | |
utslib.copyright.status | open_access | * |
pubs.consider-herdc | false | |
dc.date.updated | 2021-09-25T22:07:42Z | |
pubs.publication-status | Published | |
pubs.volume | 83 |
Abstract:
Background
Bufei Yishen formula (BYF), a traditional Chinese medicine (TCM), is an effective therapeutic strategy for patients with chronic obstructive pulmonary disease (COPD).
Purpose
To evaluate the efficacy of BYF and investigate its therapeutic mechanisms.
Methods
A total of 134 patients completed the study: 68 patients treated by BYF combined with conventional Western medicine in the trial group; and 66 patients treated using conventional Western medicine in the control group. The efficacy of BYF was evaluated by a subgroup analysis of data obtained from a four-center, open-label, randomized controlled trial of comprehensive TCM interventions. A rat model of COPD was treated with the key active molecules (KAM) of BYF for 8 weeks. An in vitro model of COPD was also treated with KAM.
Results
Patients treated with BYF had reduced frequency of acute exacerbation of COPD (p < 0.001) and duration (p = 0.028), dyspnea scale (p = 0.007), 6-min walking distance (p = 0.048). There were no differences observed in forced vital capacity in one second (FVC), forced expiratory volume in one second (FEV1), and FEV1 percentage of the predicted value (FEV1%). The five KAM of BYF (KAM-BYF) improved lung function, including tidal volume, minute ventilation, peak expiratory flow, FVC, FEV0.1, and FEV0.3, and pathological changes in COPD rats. Treatment with KAM-BYF markedly decreased the levels of interleukin 6 (IL6), tumor necrosis factor-α (TNF-α), matrix metalloproteinase 9 (MMP9), and MMP12 in serum and bronchial alveolar lavage fluid. In airway epithelial cells, KAM-BYF decreased the levels of TNF-α-induced IL8 and IL6. Finally, we discovered that the anti-inflammatory effects of KAM-BYF in COPD rats and BEAS-2Bs were mediated through inhibition of nuclear factor-kappaB (NF-κB) p65, c-Jun NH2-terminal kinase (JNK), and p38 mitogen-activated protein kinase signaling.
Conclusions
BYF exerts beneficial effects in patients with COPD via inhibition of inflammation.
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