Effective-Component Compatibility of Bufei Yishen Formula III Protects Lung Air-Blood Barrier by Regulating the Oxidative Stress: via the Nuclear Factor-E2-Related Factor 2 Pathway.

IF 2.7 3区 医学 Q2 RESPIRATORY SYSTEM
Kexin Xu, Xuejie Shao, Ruilong Lu, Yixi Liao, Yakun Zhao, Bo Wang, Zhiguang Qiu, Yange Tian
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引用次数: 0

Abstract

Purpose: Bufei Yishen formula (BYF) is an effective treatment strategy for chronic obstructive pulmonary disease (COPD). Effective-component compatibility of BYF III (ECC-BYF III), composed of 5 active ingredients (ginsenoside Rh1, paeonol, astragaloside, icariin and nobiletin) from BYF, has similar effects to BYF in intervening COPD. The abnormal structure and hypofunction of lung air-blood barrier induces inefficiency gas exchange and promotes development of COPD. However, the role of ECC-BYF III in the air-blood barrier remains unknown. This study dedicated to exploring the effect and mechanism of ECC-BYF III improve structure and function of lung air-blood barrier in COPD.

Methods: A COPD rat model was established to study the treatment of ECC-BYF III against COPD. The protective effect of ECC-BYF III on COPD was evaluated through pulmonary function and lung tissue pathology. The structure damage of the lung air-blood barrier was assessed using electron microscopy and immunofluorescence. Finally, we proved the regulating effect of ECC-BYF III in oxidative via the Nrf2 pathway.

Results: The ECC-BYF III could significantly alleviate reduced pulmonary function, decrease damage of lung tissue and regulate oxidative stress in COPD rats. And ECC-BYF III reduced thickness of respiratory membrane, ameliorated damage of pulmonary capillary endothelial cells (PCECs) and alveolar epithelial cells (AECs) in COPD rats. Also, ECC-BYF III protected the function and normal cell morphology of type I alveolar epithelial cell (AT I) and type II alveolar epithelial cell (AT II) in COPD rats. Lastly, ECC-BYF III was indicated to adjust the Nrf2 pathway to improve oxidative stress and protect lung air-blood barrier in COPD rats.

Conclusion: ECC-BYF III protects lung air-blood barrier in COPD by regulating oxidative stress via Nrf2 pathway.

补肺益肾配方III通过调节氧化应激保护肺气血屏障:通过核因子- e2相关因子2途径。
目的:补肺益肾方是治疗慢性阻塞性肺疾病(COPD)的有效方法。BYF III的有效成分相容性(ECC-BYF III)由参皂苷Rh1、丹皮酚、黄芪甲苷、淫羊藿苷、苦楝素5种有效成分组成,其干预COPD的作用与BYF相似。肺气血屏障结构异常、功能低下导致气体交换效率低下,促进COPD的发展。然而,ECC-BYF III在气血屏障中的作用尚不清楚。本研究旨在探讨ECC-BYF III改善COPD患者肺气血屏障结构和功能的作用及机制。方法:建立慢性阻塞性肺疾病大鼠模型,研究ECC-BYF III对慢性阻塞性肺疾病的治疗作用。通过肺功能和肺组织病理评价ECC-BYF III对COPD的保护作用。电镜和免疫荧光观察肺气血屏障结构损伤情况。最后,我们通过Nrf2途径证明了ECC-BYF III对氧化的调节作用。结果:ECC-BYF III能显著缓解COPD大鼠肺功能减退,减轻肺组织损伤,调节氧化应激。ECC-BYF III可降低COPD大鼠呼吸膜厚度,改善肺毛细血管内皮细胞(PCECs)和肺泡上皮细胞(AECs)损伤。此外,ECC-BYF III还能保护COPD大鼠I型肺泡上皮细胞(AT I)和II型肺泡上皮细胞(AT II)的功能和正常细胞形态。最后,研究表明ECC-BYF III可调节Nrf2通路,改善COPD大鼠氧化应激,保护肺气血屏障。结论:ECC-BYF III通过Nrf2途径调节氧化应激,对COPD肺气血屏障具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
10.70%
发文量
372
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal of therapeutics and pharmacology focusing on concise rapid reporting of clinical studies and reviews in COPD. Special focus will be given to the pathophysiological processes underlying the disease, intervention programs, patient focused education, and self management protocols. This journal is directed at specialists and healthcare professionals
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