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Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease

Alzheimer's disease (AD) is a common neurodegenerative disease, characterized by cognitive dysfunction; however, the therapeutic strategies are not fully understood. Huang-Lian-Jie-Du-Decoction (HLJDD) is a famous traditional Chinese herbal formula that has been widely used clinically to treat...

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Autores principales: Liu, Yan, Du, Ting, Zhang, Wenlong, Lu, Weiye, Peng, Zhichao, Huang, Shuqiong, Sun, Xiangdong, Zhu, Xiaoqin, Chen, Chaojun, Qian, Linchao, Wen, Lei, Xu, Pingyi, Zhang, Yunlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875425/
https://www.ncbi.nlm.nih.gov/pubmed/31781354
http://dx.doi.org/10.1155/2019/8340192
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author Liu, Yan
Du, Ting
Zhang, Wenlong
Lu, Weiye
Peng, Zhichao
Huang, Shuqiong
Sun, Xiangdong
Zhu, Xiaoqin
Chen, Chaojun
Qian, Linchao
Wen, Lei
Xu, Pingyi
Zhang, Yunlong
author_facet Liu, Yan
Du, Ting
Zhang, Wenlong
Lu, Weiye
Peng, Zhichao
Huang, Shuqiong
Sun, Xiangdong
Zhu, Xiaoqin
Chen, Chaojun
Qian, Linchao
Wen, Lei
Xu, Pingyi
Zhang, Yunlong
author_sort Liu, Yan
collection PubMed
description Alzheimer's disease (AD) is a common neurodegenerative disease, characterized by cognitive dysfunction; however, the therapeutic strategies are not fully understood. Huang-Lian-Jie-Du-Decoction (HLJDD) is a famous traditional Chinese herbal formula that has been widely used clinically to treat dementia. Recently, according to previous study and our clinical practice, we generate a new modification of HLJDD (named modified-HLJDD). In this study, we indicated that modified-HLJDD attenuated learning and memory deficiencies in Aβ(1-42) oligomer-induced AD model, and we confirmed the exact metabolites in modified-HLJDD solution, as compared with HLJDD by UHPLC-Q-TOF-MS. Using GC-Q-TOF/MS-based metabolomics, we identified adenosine as the potential significant metabolite, responsible for modified-HLJDD regulating energy metabolism and synaptic plasticity in AD model. We also revealed that the potential underlying mechanism of modified-HLJDD in AD model may involve NMDA receptor-mediated glutamatergic transmission and adenosine/ATPase/AMPK cascade. Moreover, we also indicated the differential gut microbiota which mainly involved Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria at the phylum level upon modified-HLJDD treatment in AD model. Based on the correlation of metabolomic analysis with microbiome analysis, we clarified that Dorea is the most affected microbiota with adenosine upon modified-HLJDD treatment in AD model. Thus, our study suggests that modified-HLJDD may serve as a potential therapeutic drug in treating AD.
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spelling pubmed-68754252019-11-28 Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease Liu, Yan Du, Ting Zhang, Wenlong Lu, Weiye Peng, Zhichao Huang, Shuqiong Sun, Xiangdong Zhu, Xiaoqin Chen, Chaojun Qian, Linchao Wen, Lei Xu, Pingyi Zhang, Yunlong Oxid Med Cell Longev Research Article Alzheimer's disease (AD) is a common neurodegenerative disease, characterized by cognitive dysfunction; however, the therapeutic strategies are not fully understood. Huang-Lian-Jie-Du-Decoction (HLJDD) is a famous traditional Chinese herbal formula that has been widely used clinically to treat dementia. Recently, according to previous study and our clinical practice, we generate a new modification of HLJDD (named modified-HLJDD). In this study, we indicated that modified-HLJDD attenuated learning and memory deficiencies in Aβ(1-42) oligomer-induced AD model, and we confirmed the exact metabolites in modified-HLJDD solution, as compared with HLJDD by UHPLC-Q-TOF-MS. Using GC-Q-TOF/MS-based metabolomics, we identified adenosine as the potential significant metabolite, responsible for modified-HLJDD regulating energy metabolism and synaptic plasticity in AD model. We also revealed that the potential underlying mechanism of modified-HLJDD in AD model may involve NMDA receptor-mediated glutamatergic transmission and adenosine/ATPase/AMPK cascade. Moreover, we also indicated the differential gut microbiota which mainly involved Firmicutes, Bacteroidetes, Proteobacteria, and Actinobacteria at the phylum level upon modified-HLJDD treatment in AD model. Based on the correlation of metabolomic analysis with microbiome analysis, we clarified that Dorea is the most affected microbiota with adenosine upon modified-HLJDD treatment in AD model. Thus, our study suggests that modified-HLJDD may serve as a potential therapeutic drug in treating AD. Hindawi 2019-11-03 /pmc/articles/PMC6875425/ /pubmed/31781354 http://dx.doi.org/10.1155/2019/8340192 Text en Copyright © 2019 Yan Liu et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Yan
Du, Ting
Zhang, Wenlong
Lu, Weiye
Peng, Zhichao
Huang, Shuqiong
Sun, Xiangdong
Zhu, Xiaoqin
Chen, Chaojun
Qian, Linchao
Wen, Lei
Xu, Pingyi
Zhang, Yunlong
Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease
title Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease
title_full Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease
title_fullStr Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease
title_full_unstemmed Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease
title_short Modified Huang-Lian-Jie-Du Decoction Ameliorates Aβ Synaptotoxicity in a Murine Model of Alzheimer's Disease
title_sort modified huang-lian-jie-du decoction ameliorates aβ synaptotoxicity in a murine model of alzheimer's disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875425/
https://www.ncbi.nlm.nih.gov/pubmed/31781354
http://dx.doi.org/10.1155/2019/8340192
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