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Qingfei Xiaoyan Wan alleviates asthma through multi-target network regulation

BACKGROUND: Qingfei Xiaoyan Wan (QFXY), a traditional Chinese formula, is widely used for relieving cough, asthma, upper respiratory tract infection, bronchitis, pneumonia, and etc. in clinic. Comparing with other anti-asthma drugs, it is characterised with moderate and persistent efficacy as well a...

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Autores principales: Zhao, Zhenying, Miao, Yingbo, Pan, Pengwei, Cheng, Binfeng, Bai, Gang, Wu, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765495/
https://www.ncbi.nlm.nih.gov/pubmed/23919426
http://dx.doi.org/10.1186/1472-6882-13-206
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author Zhao, Zhenying
Miao, Yingbo
Pan, Pengwei
Cheng, Binfeng
Bai, Gang
Wu, Hong
author_facet Zhao, Zhenying
Miao, Yingbo
Pan, Pengwei
Cheng, Binfeng
Bai, Gang
Wu, Hong
author_sort Zhao, Zhenying
collection PubMed
description BACKGROUND: Qingfei Xiaoyan Wan (QFXY), a traditional Chinese formula, is widely used for relieving cough, asthma, upper respiratory tract infection, bronchitis, pneumonia, and etc. in clinic. Comparing with other anti-asthma drugs, it is characterised with moderate and persistent efficacy as well as few side effects, however, the underlying action mechanism still remains elusive. This study aimed to identify QFXY multi-target network regulation as an asthma controller. METHODS: This study established asthma model induced by histamine phosphate and acetylcholine chloride (His&Ach) in guinea pigs, which then were administered orally with QFXY. Hematoxylin-Eosin staining sections were applied for evaluating QFXY effect. In both Model and QFXY groups, customized microarrays and 2D electrophoresis were adopted to detect differentially expressed genes (diff genes) and proteins (diff proteins) respectively, and some diff proteins were identified with MALDI-TOF/MS. The checked diff genes and proteins underwent Cluster, GO and KEGG analysis. Based on GAD and HPRD databases, QFXY-asthma target regulation network was constructed. RESULTS: His&Ach-induced asthma model of guinea pigs was established. HE sections presented anti-inflammation and anti-remodelling effects of QFXY. Comparing with the Model group, 55 diff genes and 6 diff proteins were identified in QFXY group. Validation by qPCR and Western blot showed the microarray and 2D data reliable. Furthermore, QFXY-asthma target regulation network was achieved. CONCLUSIONS: A primarily combined genomic and proteomic screening of QFXY targets displayed a series of candidate genes and proteins, which indicated that the effect of QFXY relied on the combined mechanism, anti-inflammation and anti-remodelling, as well as influencing signal transduction in vivo.
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spelling pubmed-37654952013-09-08 Qingfei Xiaoyan Wan alleviates asthma through multi-target network regulation Zhao, Zhenying Miao, Yingbo Pan, Pengwei Cheng, Binfeng Bai, Gang Wu, Hong BMC Complement Altern Med Research Article BACKGROUND: Qingfei Xiaoyan Wan (QFXY), a traditional Chinese formula, is widely used for relieving cough, asthma, upper respiratory tract infection, bronchitis, pneumonia, and etc. in clinic. Comparing with other anti-asthma drugs, it is characterised with moderate and persistent efficacy as well as few side effects, however, the underlying action mechanism still remains elusive. This study aimed to identify QFXY multi-target network regulation as an asthma controller. METHODS: This study established asthma model induced by histamine phosphate and acetylcholine chloride (His&Ach) in guinea pigs, which then were administered orally with QFXY. Hematoxylin-Eosin staining sections were applied for evaluating QFXY effect. In both Model and QFXY groups, customized microarrays and 2D electrophoresis were adopted to detect differentially expressed genes (diff genes) and proteins (diff proteins) respectively, and some diff proteins were identified with MALDI-TOF/MS. The checked diff genes and proteins underwent Cluster, GO and KEGG analysis. Based on GAD and HPRD databases, QFXY-asthma target regulation network was constructed. RESULTS: His&Ach-induced asthma model of guinea pigs was established. HE sections presented anti-inflammation and anti-remodelling effects of QFXY. Comparing with the Model group, 55 diff genes and 6 diff proteins were identified in QFXY group. Validation by qPCR and Western blot showed the microarray and 2D data reliable. Furthermore, QFXY-asthma target regulation network was achieved. CONCLUSIONS: A primarily combined genomic and proteomic screening of QFXY targets displayed a series of candidate genes and proteins, which indicated that the effect of QFXY relied on the combined mechanism, anti-inflammation and anti-remodelling, as well as influencing signal transduction in vivo. BioMed Central 2013-08-06 /pmc/articles/PMC3765495/ /pubmed/23919426 http://dx.doi.org/10.1186/1472-6882-13-206 Text en Copyright © 2013 Zhao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhao, Zhenying
Miao, Yingbo
Pan, Pengwei
Cheng, Binfeng
Bai, Gang
Wu, Hong
Qingfei Xiaoyan Wan alleviates asthma through multi-target network regulation
title Qingfei Xiaoyan Wan alleviates asthma through multi-target network regulation
title_full Qingfei Xiaoyan Wan alleviates asthma through multi-target network regulation
title_fullStr Qingfei Xiaoyan Wan alleviates asthma through multi-target network regulation
title_full_unstemmed Qingfei Xiaoyan Wan alleviates asthma through multi-target network regulation
title_short Qingfei Xiaoyan Wan alleviates asthma through multi-target network regulation
title_sort qingfei xiaoyan wan alleviates asthma through multi-target network regulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3765495/
https://www.ncbi.nlm.nih.gov/pubmed/23919426
http://dx.doi.org/10.1186/1472-6882-13-206
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