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补肺活血胶囊减轻小鼠PM2.5诱导的肺部炎症

Bufei Huoxue Capsule Attenuates PM2.5-Induced Pulmonary Inflammation in Mice.

作者信息

Jing Yue, Zhang Hongchun, Cai Zhe, Zhao Yukun, Wu Ye, Zheng Xuan, Liu Ying, Qin Yuying, Gu Mingjie, Jin Jin

机构信息

Graduate School, Beijing University of Chinese Medicine, 11 North 3rd Ring East Road, Chaoyang District, Beijing 100029, China; National Clinical Research Center for Respiratory Diseases and Traditional Chinese Medicine Department of Pulmonary Diseases, China-Japan Friendship Hospital, 2 Yinghua Dongjie, Hepingli, Chaoyang District, Beijing 100029, China.

National Clinical Research Center for Respiratory Diseases and Traditional Chinese Medicine Department of Pulmonary Diseases, China-Japan Friendship Hospital, 2 Yinghua Dongjie, Hepingli, Chaoyang District, Beijing 100029, China.

出版信息

Evid Based Complement Alternat Med. 2017;2017:1575793. doi: 10.1155/2017/1575793. Epub 2017 Feb 27.

Abstract

Atmospheric fine particulate matter 2.5 (PM 2.5) may carry many toxic substances on its surface and this may pose a public health threat. Epidemiological research indicates that cumulative ambient PM2.5 is correlated to morbidity and mortality due to pulmonary and cardiovascular diseases and cancer. Mitigating the toxic effects of PM2.5 is therefore highly desired. Bufei Huoxue (BFHX) capsules have been used in China to treat pulmonary heart disease (cor pulmonale). Thus, we assessed the effects of BFHX capsules on PM2.5-induced pulmonary inflammation and the underlying mechanisms of action. Using Polysearch and Cytoscape 3.2.1 software, pharmacological targets of BFHX capsules in atmospheric PM2.5-related respiratory disorders were predicted and found to be related to biological pathways of inflammation and immune function. In a mouse model of PM2.5-induced inflammation established with intranasal instillation of PM2.5 suspension, BFHX significantly reduced pathological response and inflammatory mediators including IL-4, IL-6, IL-10, IL-8, TNF-, and IL-1. BFHX also reduced keratinocyte growth factor (KGF), secretory immunoglobulin A (sIgA), and collagen fibers deposition in lung and improved lung function. Thus, BFHX reduced pathological responses induced by PM2.5, possibly via regulation of inflammatory mediators in mouse lungs.

摘要

大气细颗粒物2.5(PM 2.5)表面可能携带多种有毒物质,这可能对公众健康构成威胁。流行病学研究表明,环境中PM2.5的累积量与肺部、心血管疾病及癌症导致的发病率和死亡率相关。因此,减轻PM2.5的毒性作用非常必要。补肺活血(BFHX)胶囊在中国已被用于治疗肺心病。因此,我们评估了BFHX胶囊对PM2.5诱导的肺部炎症的影响及其潜在作用机制。使用Polysearch和Cytoscape 3.2.1软件,预测了BFHX胶囊在大气PM2.5相关呼吸系统疾病中的药理靶点,发现其与炎症和免疫功能的生物学途径有关。在用滴鼻法给小鼠滴注PM2.5悬浮液建立的PM2.5诱导炎症小鼠模型中,BFHX显著减轻了病理反应和炎症介质水平,这些炎症介质包括白细胞介素-4(IL-4)、白细胞介素-6(IL-6)、白细胞介素-10(IL-10)、白细胞介素-8(IL-8)、肿瘤坏死因子-α(TNF-α)和白细胞介素-1(IL-1)。BFHX还降低了角质形成细胞生长因子(KGF)、分泌型免疫球蛋白A(sIgA)水平,并减少了肺中胶原纤维沉积,改善了肺功能。因此,BFHX可能通过调节小鼠肺中的炎症介质减轻了PM2.5诱导的病理反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4ae/5350288/686a4ef83edb/ECAM2017-1575793.001.jpg

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