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Network pharmacology-based study on the mechanism of Schisandra chinensis for treating Alzheimer's disease

BACKGROUND: Alzheimer's disease (AD) is a mental illness that poses a serious threat to human health worldwide. Schisandra chinensis is a natural herb that can treat the effects of AD, but its specific mechanism is still unclear. The purpose of this study was to explore the potential components...

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Autores principales: Kun, Cheng, Feiyi, Sun, Jian, Dong, Feng, Chen, Guihua, Wu, Jiangping, Zhu, Jianwu, Ji, Hong, Liu, Xiaowei, Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282681/
https://www.ncbi.nlm.nih.gov/pubmed/32565596
http://dx.doi.org/10.4103/ijp.IJP_515_19
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author Kun, Cheng
Feiyi, Sun
Jian, Dong
Feng, Chen
Guihua, Wu
Jiangping, Zhu
Jianwu, Ji
Hong, Liu
Xiaowei, Han
author_facet Kun, Cheng
Feiyi, Sun
Jian, Dong
Feng, Chen
Guihua, Wu
Jiangping, Zhu
Jianwu, Ji
Hong, Liu
Xiaowei, Han
author_sort Kun, Cheng
collection PubMed
description BACKGROUND: Alzheimer's disease (AD) is a mental illness that poses a serious threat to human health worldwide. Schisandra chinensis is a natural herb that can treat the effects of AD, but its specific mechanism is still unclear. The purpose of this study was to explore the potential components and pharmacological pathways of S. chinensis in the treatment of AD. MATERIALS AND METHODS: In this study, we investigated the compound of S. chinensis and the effects of it on AD by network pharmacology. Meanwhile, the potential mechanism was proved in vitro. RESULTS: The results showed that S. chinensis contained 173 compounds. Compound-target network confirmed that (E)-9-Isopropyl-6-Methyl-5,9-Decadiene-2-One, 1-Phenyl-1,3-Butanedion, nootkatone and phenyl-2-Propanone were the main chemical constituents which highly aimed at APOE, CACNA1D, GRIN2A, and PTGS2. KEGG and GO enrichment analysis indicated that the main pathways involved neural-related signaling pathways and functions, such as nicotine addiction, GABAergic synapse, Ca(2+) signaling pathway, AD, and so on. Validation experiments showed that nootkatone was able to exert anti-apoptotic effects related to Ca(2+) signaling pathway by inhibiting nitric oxide production, enhancing the activity of antioxidant enzymes, upregulating the expression of anti-oxidation and anti-apoptotic proteins in vitro. CONCLUSIONS: These results illustrated that S. chinensis could regulate neuronal apoptosis through the calcium signaling pathway to exert anti-AD by integrating multi-component, multi-target and multi-pathway.
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spelling pubmed-72826812020-06-19 Network pharmacology-based study on the mechanism of Schisandra chinensis for treating Alzheimer's disease Kun, Cheng Feiyi, Sun Jian, Dong Feng, Chen Guihua, Wu Jiangping, Zhu Jianwu, Ji Hong, Liu Xiaowei, Han Indian J Pharmacol Experimental Research Article BACKGROUND: Alzheimer's disease (AD) is a mental illness that poses a serious threat to human health worldwide. Schisandra chinensis is a natural herb that can treat the effects of AD, but its specific mechanism is still unclear. The purpose of this study was to explore the potential components and pharmacological pathways of S. chinensis in the treatment of AD. MATERIALS AND METHODS: In this study, we investigated the compound of S. chinensis and the effects of it on AD by network pharmacology. Meanwhile, the potential mechanism was proved in vitro. RESULTS: The results showed that S. chinensis contained 173 compounds. Compound-target network confirmed that (E)-9-Isopropyl-6-Methyl-5,9-Decadiene-2-One, 1-Phenyl-1,3-Butanedion, nootkatone and phenyl-2-Propanone were the main chemical constituents which highly aimed at APOE, CACNA1D, GRIN2A, and PTGS2. KEGG and GO enrichment analysis indicated that the main pathways involved neural-related signaling pathways and functions, such as nicotine addiction, GABAergic synapse, Ca(2+) signaling pathway, AD, and so on. Validation experiments showed that nootkatone was able to exert anti-apoptotic effects related to Ca(2+) signaling pathway by inhibiting nitric oxide production, enhancing the activity of antioxidant enzymes, upregulating the expression of anti-oxidation and anti-apoptotic proteins in vitro. CONCLUSIONS: These results illustrated that S. chinensis could regulate neuronal apoptosis through the calcium signaling pathway to exert anti-AD by integrating multi-component, multi-target and multi-pathway. Wolters Kluwer - Medknow 2020 2020-06-03 /pmc/articles/PMC7282681/ /pubmed/32565596 http://dx.doi.org/10.4103/ijp.IJP_515_19 Text en Copyright: © 2020 Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Experimental Research Article
Kun, Cheng
Feiyi, Sun
Jian, Dong
Feng, Chen
Guihua, Wu
Jiangping, Zhu
Jianwu, Ji
Hong, Liu
Xiaowei, Han
Network pharmacology-based study on the mechanism of Schisandra chinensis for treating Alzheimer's disease
title Network pharmacology-based study on the mechanism of Schisandra chinensis for treating Alzheimer's disease
title_full Network pharmacology-based study on the mechanism of Schisandra chinensis for treating Alzheimer's disease
title_fullStr Network pharmacology-based study on the mechanism of Schisandra chinensis for treating Alzheimer's disease
title_full_unstemmed Network pharmacology-based study on the mechanism of Schisandra chinensis for treating Alzheimer's disease
title_short Network pharmacology-based study on the mechanism of Schisandra chinensis for treating Alzheimer's disease
title_sort network pharmacology-based study on the mechanism of schisandra chinensis for treating alzheimer's disease
topic Experimental Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282681/
https://www.ncbi.nlm.nih.gov/pubmed/32565596
http://dx.doi.org/10.4103/ijp.IJP_515_19
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