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Xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation
An overarching consequence of traumatic brain injury (TBI) is the cognitive impairment. It may hinder individual performance of daily tasks and determine people's subjective well-being. The damage to synaptic plasticity, one of the key mechanisms of cognitive dysfunction, becomes the potential...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641112/ https://www.ncbi.nlm.nih.gov/pubmed/29069769 http://dx.doi.org/10.18632/oncotarget.18895 |
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author | Zhou, Jing Liu, Tao Cui, Hanjin Fan, Rong Zhang, Chunhu Peng, Weijun Yang, Ali Zhu, Lin Wang, Yang Tang, Tao |
author_facet | Zhou, Jing Liu, Tao Cui, Hanjin Fan, Rong Zhang, Chunhu Peng, Weijun Yang, Ali Zhu, Lin Wang, Yang Tang, Tao |
author_sort | Zhou, Jing |
collection | PubMed |
description | An overarching consequence of traumatic brain injury (TBI) is the cognitive impairment. It may hinder individual performance of daily tasks and determine people's subjective well-being. The damage to synaptic plasticity, one of the key mechanisms of cognitive dysfunction, becomes the potential therapeutic strategy of TBI. In this study, we aimed to investigate whether Xuefu Zhuyu Decoction (XFZYD), a traditional Chinese medicine, provided a synaptic regulation to improve cognitive disorder following TBI. Morris water maze and modified neurological severity scores were performed to assess the neurological and cognitive abilities. The PubChem Compound IDs of the major compounds of XFZYD were submitted into BATMAN-TCM, an online bioinformatics analysis tool, to predict the druggable targets related to synaptic function. Furthermore, we validated the prediction through immunohistochemical, RT-PCR and western blot analyses. We found that XFZYD enhanced neuroprotection, simultaneously improved learning and memory performances in controlled cortical impact rats. Bioinformatics analysis revealed that the improvements of XFZYD implied the Long-term potentiation relative proteins including NMDAR1, CaMKII and GAP-43. The further confirmation of molecular biological studies confirmed that XFZYD upregulated the mRNA and protein levels of NMDAR1, CaMKII and GAP-43. Pharmacological synaptic regulation of XFZYD could provide a novel therapeutic strategy for cognitive impairment following TBI. |
format | Online Article Text |
id | pubmed-5641112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56411122017-10-24 Xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation Zhou, Jing Liu, Tao Cui, Hanjin Fan, Rong Zhang, Chunhu Peng, Weijun Yang, Ali Zhu, Lin Wang, Yang Tang, Tao Oncotarget Research Paper An overarching consequence of traumatic brain injury (TBI) is the cognitive impairment. It may hinder individual performance of daily tasks and determine people's subjective well-being. The damage to synaptic plasticity, one of the key mechanisms of cognitive dysfunction, becomes the potential therapeutic strategy of TBI. In this study, we aimed to investigate whether Xuefu Zhuyu Decoction (XFZYD), a traditional Chinese medicine, provided a synaptic regulation to improve cognitive disorder following TBI. Morris water maze and modified neurological severity scores were performed to assess the neurological and cognitive abilities. The PubChem Compound IDs of the major compounds of XFZYD were submitted into BATMAN-TCM, an online bioinformatics analysis tool, to predict the druggable targets related to synaptic function. Furthermore, we validated the prediction through immunohistochemical, RT-PCR and western blot analyses. We found that XFZYD enhanced neuroprotection, simultaneously improved learning and memory performances in controlled cortical impact rats. Bioinformatics analysis revealed that the improvements of XFZYD implied the Long-term potentiation relative proteins including NMDAR1, CaMKII and GAP-43. The further confirmation of molecular biological studies confirmed that XFZYD upregulated the mRNA and protein levels of NMDAR1, CaMKII and GAP-43. Pharmacological synaptic regulation of XFZYD could provide a novel therapeutic strategy for cognitive impairment following TBI. Impact Journals LLC 2017-06-30 /pmc/articles/PMC5641112/ /pubmed/29069769 http://dx.doi.org/10.18632/oncotarget.18895 Text en Copyright: © 2017 Zhou et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Zhou, Jing Liu, Tao Cui, Hanjin Fan, Rong Zhang, Chunhu Peng, Weijun Yang, Ali Zhu, Lin Wang, Yang Tang, Tao Xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation |
title | Xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation |
title_full | Xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation |
title_fullStr | Xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation |
title_full_unstemmed | Xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation |
title_short | Xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation |
title_sort | xuefu zhuyu decoction improves cognitive impairment in experimental traumatic brain injury via synaptic regulation |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641112/ https://www.ncbi.nlm.nih.gov/pubmed/29069769 http://dx.doi.org/10.18632/oncotarget.18895 |
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