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

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....

Full description

Bibliographic Details
Main Authors: Yue Jing, Hongchun Zhang, Zhe Cai, Yukun Zhao, Ye Wu, Xuan Zheng, Ying Liu, Yuying Qin, Mingjie Gu, Jin Jin
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Evidence-Based Complementary and Alternative Medicine
Online Access:http://dx.doi.org/10.1155/2017/1575793
id doaj-61299629505947388566bf2b3295a53e
record_format Article
spelling doaj-61299629505947388566bf2b3295a53e2020-11-24T22:41:34ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882017-01-01201710.1155/2017/15757931575793Bufei Huoxue Capsule Attenuates PM2.5-Induced Pulmonary Inflammation in MiceYue Jing0Hongchun Zhang1Zhe Cai2Yukun Zhao3Ye Wu4Xuan Zheng5Ying Liu6Yuying Qin7Mingjie Gu8Jin Jin9Graduate School, Beijing University of Chinese Medicine, 11 North 3rd Ring East Road, Chaoyang District, Beijing 100029, ChinaNational 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, ChinaClinical Research Institute, China-Japan Friendship Hospital, 2 Yinghua Dongjie, Hepingli, Chaoyang District, Beijing 100029, ChinaInstitute of Basic Theory for Chinese Medicine, China Academy of Chinese Medical Science, 16 Dongzhimennei Nanxiaojie, Dongcheng District, Beijing 100700, ChinaSchool of Environment, State Key Joint Laboratory of Environment Simulation and Pollution Control, Tsinghua University, Beijing 100084, ChinaSchool of Environment, State Key Joint Laboratory of Environment Simulation and Pollution Control, Tsinghua University, Beijing 100084, ChinaGeriatrics, China-Japan Friendship Hospital, 2 Yinghua Dongjie, Hepingli, Chaoyang District, Beijing 100029, ChinaGraduate School, Beijing University of Chinese Medicine, 11 North 3rd Ring East Road, Chaoyang District, Beijing 100029, ChinaGraduate School, Beijing University of Chinese Medicine, 11 North 3rd Ring East Road, Chaoyang District, Beijing 100029, ChinaGraduate School, Beijing University of Chinese Medicine, 11 North 3rd Ring East Road, Chaoyang District, Beijing 100029, ChinaAtmospheric 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-α, and IL-1β. 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.http://dx.doi.org/10.1155/2017/1575793
collection DOAJ
language English
format Article
sources DOAJ
author Yue Jing
Hongchun Zhang
Zhe Cai
Yukun Zhao
Ye Wu
Xuan Zheng
Ying Liu
Yuying Qin
Mingjie Gu
Jin Jin
spellingShingle Yue Jing
Hongchun Zhang
Zhe Cai
Yukun Zhao
Ye Wu
Xuan Zheng
Ying Liu
Yuying Qin
Mingjie Gu
Jin Jin
Bufei Huoxue Capsule Attenuates PM2.5-Induced Pulmonary Inflammation in Mice
Evidence-Based Complementary and Alternative Medicine
author_facet Yue Jing
Hongchun Zhang
Zhe Cai
Yukun Zhao
Ye Wu
Xuan Zheng
Ying Liu
Yuying Qin
Mingjie Gu
Jin Jin
author_sort Yue Jing
title Bufei Huoxue Capsule Attenuates PM2.5-Induced Pulmonary Inflammation in Mice
title_short Bufei Huoxue Capsule Attenuates PM2.5-Induced Pulmonary Inflammation in Mice
title_full Bufei Huoxue Capsule Attenuates PM2.5-Induced Pulmonary Inflammation in Mice
title_fullStr Bufei Huoxue Capsule Attenuates PM2.5-Induced Pulmonary Inflammation in Mice
title_full_unstemmed Bufei Huoxue Capsule Attenuates PM2.5-Induced Pulmonary Inflammation in Mice
title_sort bufei huoxue capsule attenuates pm2.5-induced pulmonary inflammation in mice
publisher Hindawi Limited
series Evidence-Based Complementary and Alternative Medicine
issn 1741-427X
1741-4288
publishDate 2017-01-01
description 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-α, and IL-1β. 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.
url http://dx.doi.org/10.1155/2017/1575793
work_keys_str_mv AT yuejing bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT hongchunzhang bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT zhecai bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT yukunzhao bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT yewu bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT xuanzheng bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT yingliu bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT yuyingqin bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT mingjiegu bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
AT jinjin bufeihuoxuecapsuleattenuatespm25inducedpulmonaryinflammationinmice
_version_ 1725701824694976512