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Multiplex Brain Proteomic Analysis Revealed the Molecular Therapeutic Effects of Buyang Huanwu Decoction on Cerebral Ischemic Stroke Mice

Stroke is the second-leading cause of death worldwide, and tissue plasminogen activator (TPA) is the only drug used for a limited group of stroke patients in the acute phase. Buyang Huanwu Decoction (BHD), a traditional Chinese medicine prescription, has long been used for improving neurological fun...

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Autores principales: Chen, Hong-Jhang, Shen, Yuh-Chiang, Shiao, Young-Ji, Liou, Kuo-Tong, Hsu, Wei-Hsiang, Hsieh, Pei-Hsuan, Lee, Chi-Ying, Chen, Yet-Ran, Lin, Yun-Lian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619651/
https://www.ncbi.nlm.nih.gov/pubmed/26492191
http://dx.doi.org/10.1371/journal.pone.0140823
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author Chen, Hong-Jhang
Shen, Yuh-Chiang
Shiao, Young-Ji
Liou, Kuo-Tong
Hsu, Wei-Hsiang
Hsieh, Pei-Hsuan
Lee, Chi-Ying
Chen, Yet-Ran
Lin, Yun-Lian
author_facet Chen, Hong-Jhang
Shen, Yuh-Chiang
Shiao, Young-Ji
Liou, Kuo-Tong
Hsu, Wei-Hsiang
Hsieh, Pei-Hsuan
Lee, Chi-Ying
Chen, Yet-Ran
Lin, Yun-Lian
author_sort Chen, Hong-Jhang
collection PubMed
description Stroke is the second-leading cause of death worldwide, and tissue plasminogen activator (TPA) is the only drug used for a limited group of stroke patients in the acute phase. Buyang Huanwu Decoction (BHD), a traditional Chinese medicine prescription, has long been used for improving neurological functional recovery in stroke. In this study, we characterized the therapeutic effect of TPA and BHD in a cerebral ischemia/reperfusion (CIR) injury mouse model using multiplex proteomics approach. After the iTRAQ-based proteomics analysis, 1310 proteins were identified from the mouse brain with <1% false discovery rate. Among them, 877 quantitative proteins, 10.26% (90/877), 1.71% (15/877), and 2.62% (23/877) of the proteins was significantly changed in the CIR, BHD treatment, and TPA treatment, respectively. Functional categorization analysis showed that BHD treatment preserved the integrity of the blood–brain barrier (BBB) (Alb, Fga, and Trf), suppressed excitotoxicity (Grm5, Gnai, and Gdi), and enhanced energy metabolism (Bdh), thereby revealing its multiple effects on ischemic stroke mice. Moreover, the neurogenesis marker doublecortin was upregulated, and the activity of glycogen synthase kinase 3 (GSK-3) and Tau was inhibited, which represented the neuroprotective effects. However, TPA treatment deteriorated BBB breakdown. This study highlights the potential of BHD in clinical applications for ischemic stroke.
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spelling pubmed-46196512015-10-29 Multiplex Brain Proteomic Analysis Revealed the Molecular Therapeutic Effects of Buyang Huanwu Decoction on Cerebral Ischemic Stroke Mice Chen, Hong-Jhang Shen, Yuh-Chiang Shiao, Young-Ji Liou, Kuo-Tong Hsu, Wei-Hsiang Hsieh, Pei-Hsuan Lee, Chi-Ying Chen, Yet-Ran Lin, Yun-Lian PLoS One Research Article Stroke is the second-leading cause of death worldwide, and tissue plasminogen activator (TPA) is the only drug used for a limited group of stroke patients in the acute phase. Buyang Huanwu Decoction (BHD), a traditional Chinese medicine prescription, has long been used for improving neurological functional recovery in stroke. In this study, we characterized the therapeutic effect of TPA and BHD in a cerebral ischemia/reperfusion (CIR) injury mouse model using multiplex proteomics approach. After the iTRAQ-based proteomics analysis, 1310 proteins were identified from the mouse brain with <1% false discovery rate. Among them, 877 quantitative proteins, 10.26% (90/877), 1.71% (15/877), and 2.62% (23/877) of the proteins was significantly changed in the CIR, BHD treatment, and TPA treatment, respectively. Functional categorization analysis showed that BHD treatment preserved the integrity of the blood–brain barrier (BBB) (Alb, Fga, and Trf), suppressed excitotoxicity (Grm5, Gnai, and Gdi), and enhanced energy metabolism (Bdh), thereby revealing its multiple effects on ischemic stroke mice. Moreover, the neurogenesis marker doublecortin was upregulated, and the activity of glycogen synthase kinase 3 (GSK-3) and Tau was inhibited, which represented the neuroprotective effects. However, TPA treatment deteriorated BBB breakdown. This study highlights the potential of BHD in clinical applications for ischemic stroke. Public Library of Science 2015-10-22 /pmc/articles/PMC4619651/ /pubmed/26492191 http://dx.doi.org/10.1371/journal.pone.0140823 Text en © 2015 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chen, Hong-Jhang
Shen, Yuh-Chiang
Shiao, Young-Ji
Liou, Kuo-Tong
Hsu, Wei-Hsiang
Hsieh, Pei-Hsuan
Lee, Chi-Ying
Chen, Yet-Ran
Lin, Yun-Lian
Multiplex Brain Proteomic Analysis Revealed the Molecular Therapeutic Effects of Buyang Huanwu Decoction on Cerebral Ischemic Stroke Mice
title Multiplex Brain Proteomic Analysis Revealed the Molecular Therapeutic Effects of Buyang Huanwu Decoction on Cerebral Ischemic Stroke Mice
title_full Multiplex Brain Proteomic Analysis Revealed the Molecular Therapeutic Effects of Buyang Huanwu Decoction on Cerebral Ischemic Stroke Mice
title_fullStr Multiplex Brain Proteomic Analysis Revealed the Molecular Therapeutic Effects of Buyang Huanwu Decoction on Cerebral Ischemic Stroke Mice
title_full_unstemmed Multiplex Brain Proteomic Analysis Revealed the Molecular Therapeutic Effects of Buyang Huanwu Decoction on Cerebral Ischemic Stroke Mice
title_short Multiplex Brain Proteomic Analysis Revealed the Molecular Therapeutic Effects of Buyang Huanwu Decoction on Cerebral Ischemic Stroke Mice
title_sort multiplex brain proteomic analysis revealed the molecular therapeutic effects of buyang huanwu decoction on cerebral ischemic stroke mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619651/
https://www.ncbi.nlm.nih.gov/pubmed/26492191
http://dx.doi.org/10.1371/journal.pone.0140823
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