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The Mechanisms of Bushen-Yizhi Formula as a Therapeutic Agent against Alzheimer’s Disease
Bushen-Yizhi prescription (BSYZ) has been an effective traditional Chinese medicine (TCM) prescription in treating Alzheimer’s disease (AD) for hundreds of years. However, the underlying mechanisms have not been fully elucidated yet. In this work, a systems pharmacology approach was developed to rev...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814461/ https://www.ncbi.nlm.nih.gov/pubmed/29449587 http://dx.doi.org/10.1038/s41598-018-21468-w |
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author | Cai, Haobin Luo, Yunxia Yan, Xin Ding, Peng Huang, Yujie Fang, Shuhuan Zhang, Rong Chen, Yunbo Guo, Zhouke Fang, Jiansong Wang, Qi Xu, Jun |
author_facet | Cai, Haobin Luo, Yunxia Yan, Xin Ding, Peng Huang, Yujie Fang, Shuhuan Zhang, Rong Chen, Yunbo Guo, Zhouke Fang, Jiansong Wang, Qi Xu, Jun |
author_sort | Cai, Haobin |
collection | PubMed |
description | Bushen-Yizhi prescription (BSYZ) has been an effective traditional Chinese medicine (TCM) prescription in treating Alzheimer’s disease (AD) for hundreds of years. However, the underlying mechanisms have not been fully elucidated yet. In this work, a systems pharmacology approach was developed to reveal the underlying molecular mechanisms of BSYZ in treating AD. First, we obtained 329 candidate compounds of BSYZ by in silico ADME/T filter analysis and 138 AD-related targets were predicted by our in-house WEGA algorithm via mapping predicted targets into AD-related proteins. In addition, we elucidated the mechanisms of BSYZ action on AD through multiple network analysis, including compound-target network analysis and target-function network analysis. Furthermore, several modules regulated by BSYZ were incorporated into AD-related pathways to uncover the therapeutic mechanisms of this prescription in AD treatment. Finally, further verification experiments also demonstrated the therapeutic effects of BSYZ on cognitive dysfunction in APP/PS1 mice, which was possibly via regulating amyloid-β metabolism and suppressing neuronal apoptosis. In conclusion, we provide an integrative systems pharmacology approach to illustrate the underlying therapeutic mechanisms of BSYZ formula action on AD. |
format | Online Article Text |
id | pubmed-5814461 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58144612018-02-21 The Mechanisms of Bushen-Yizhi Formula as a Therapeutic Agent against Alzheimer’s Disease Cai, Haobin Luo, Yunxia Yan, Xin Ding, Peng Huang, Yujie Fang, Shuhuan Zhang, Rong Chen, Yunbo Guo, Zhouke Fang, Jiansong Wang, Qi Xu, Jun Sci Rep Article Bushen-Yizhi prescription (BSYZ) has been an effective traditional Chinese medicine (TCM) prescription in treating Alzheimer’s disease (AD) for hundreds of years. However, the underlying mechanisms have not been fully elucidated yet. In this work, a systems pharmacology approach was developed to reveal the underlying molecular mechanisms of BSYZ in treating AD. First, we obtained 329 candidate compounds of BSYZ by in silico ADME/T filter analysis and 138 AD-related targets were predicted by our in-house WEGA algorithm via mapping predicted targets into AD-related proteins. In addition, we elucidated the mechanisms of BSYZ action on AD through multiple network analysis, including compound-target network analysis and target-function network analysis. Furthermore, several modules regulated by BSYZ were incorporated into AD-related pathways to uncover the therapeutic mechanisms of this prescription in AD treatment. Finally, further verification experiments also demonstrated the therapeutic effects of BSYZ on cognitive dysfunction in APP/PS1 mice, which was possibly via regulating amyloid-β metabolism and suppressing neuronal apoptosis. In conclusion, we provide an integrative systems pharmacology approach to illustrate the underlying therapeutic mechanisms of BSYZ formula action on AD. Nature Publishing Group UK 2018-02-15 /pmc/articles/PMC5814461/ /pubmed/29449587 http://dx.doi.org/10.1038/s41598-018-21468-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cai, Haobin Luo, Yunxia Yan, Xin Ding, Peng Huang, Yujie Fang, Shuhuan Zhang, Rong Chen, Yunbo Guo, Zhouke Fang, Jiansong Wang, Qi Xu, Jun The Mechanisms of Bushen-Yizhi Formula as a Therapeutic Agent against Alzheimer’s Disease |
title | The Mechanisms of Bushen-Yizhi Formula as a Therapeutic Agent against Alzheimer’s Disease |
title_full | The Mechanisms of Bushen-Yizhi Formula as a Therapeutic Agent against Alzheimer’s Disease |
title_fullStr | The Mechanisms of Bushen-Yizhi Formula as a Therapeutic Agent against Alzheimer’s Disease |
title_full_unstemmed | The Mechanisms of Bushen-Yizhi Formula as a Therapeutic Agent against Alzheimer’s Disease |
title_short | The Mechanisms of Bushen-Yizhi Formula as a Therapeutic Agent against Alzheimer’s Disease |
title_sort | mechanisms of bushen-yizhi formula as a therapeutic agent against alzheimer’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5814461/ https://www.ncbi.nlm.nih.gov/pubmed/29449587 http://dx.doi.org/10.1038/s41598-018-21468-w |
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