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Exploring the mechanism of Semen Strychni in treating amyotrophic lateral sclerosis based on network pharmacology

Semen Strychni (SS), known as an agonist of central nervous system, is a traditional herb widely used in treating amyotrophic lateral sclerosis (ALS) in small doses to relieve muscle weakness and improve muscle strength. However, the potential mechanisms and the main components of SS in treating ALS...

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Autores principales: Tang, Xiaohui, Zhan, Yingshi, Yang, Biying, Du, Baoxin, Huang, Jingyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10489316/
https://www.ncbi.nlm.nih.gov/pubmed/37682161
http://dx.doi.org/10.1097/MD.0000000000035101
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author Tang, Xiaohui
Zhan, Yingshi
Yang, Biying
Du, Baoxin
Huang, Jingyan
author_facet Tang, Xiaohui
Zhan, Yingshi
Yang, Biying
Du, Baoxin
Huang, Jingyan
author_sort Tang, Xiaohui
collection PubMed
description Semen Strychni (SS), known as an agonist of central nervous system, is a traditional herb widely used in treating amyotrophic lateral sclerosis (ALS) in small doses to relieve muscle weakness and improve muscle strength. However, the potential mechanisms and the main components of SS in treating ALS remain unclear. To explore the underlying mechanism of SS in treating ALS based on network pharmacology and molecular docking. The active components of SS were obtained using TCMSP, Herb, ETCM, and BATMAN-TCM. The targets of SS were gained from PharmMapper. The targets of ALS were searched on Genecards, Drugbank, DisGeNET, OMIM, TTD and GEO database. After obtaining the coincidence targets, we submitted them to the STRING database to build a protein-protein interaction network. Gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were performed subsequently. The active components and targets were further investigated using molecular docking technology. 395 targets of SS and 1925 targets of ALS were obtained with 125 common targets. The protein-protein interaction analysis indicated that SRC, AKT1, MAPK1, EGFR, and HSP90AA1 received the higher degree value and were considered the central genes. The Ras, PI3K-Akt, and MAPK signaling pathway could be involved in the treatment of ALS. Brucine-N-oxide obtained the lowest binding energy in molecular docking. This study explored the mechanism of SS in the treatment of ALS and provides a new perspective for future study. However, further experimental studies are needed to validate the therapeutic effect.
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spelling pubmed-104893162023-09-09 Exploring the mechanism of Semen Strychni in treating amyotrophic lateral sclerosis based on network pharmacology Tang, Xiaohui Zhan, Yingshi Yang, Biying Du, Baoxin Huang, Jingyan Medicine (Baltimore) Research Article: Observational Study Semen Strychni (SS), known as an agonist of central nervous system, is a traditional herb widely used in treating amyotrophic lateral sclerosis (ALS) in small doses to relieve muscle weakness and improve muscle strength. However, the potential mechanisms and the main components of SS in treating ALS remain unclear. To explore the underlying mechanism of SS in treating ALS based on network pharmacology and molecular docking. The active components of SS were obtained using TCMSP, Herb, ETCM, and BATMAN-TCM. The targets of SS were gained from PharmMapper. The targets of ALS were searched on Genecards, Drugbank, DisGeNET, OMIM, TTD and GEO database. After obtaining the coincidence targets, we submitted them to the STRING database to build a protein-protein interaction network. Gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis were performed subsequently. The active components and targets were further investigated using molecular docking technology. 395 targets of SS and 1925 targets of ALS were obtained with 125 common targets. The protein-protein interaction analysis indicated that SRC, AKT1, MAPK1, EGFR, and HSP90AA1 received the higher degree value and were considered the central genes. The Ras, PI3K-Akt, and MAPK signaling pathway could be involved in the treatment of ALS. Brucine-N-oxide obtained the lowest binding energy in molecular docking. This study explored the mechanism of SS in the treatment of ALS and provides a new perspective for future study. However, further experimental studies are needed to validate the therapeutic effect. Lippincott Williams & Wilkins 2023-09-08 /pmc/articles/PMC10489316/ /pubmed/37682161 http://dx.doi.org/10.1097/MD.0000000000035101 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle Research Article: Observational Study
Tang, Xiaohui
Zhan, Yingshi
Yang, Biying
Du, Baoxin
Huang, Jingyan
Exploring the mechanism of Semen Strychni in treating amyotrophic lateral sclerosis based on network pharmacology
title Exploring the mechanism of Semen Strychni in treating amyotrophic lateral sclerosis based on network pharmacology
title_full Exploring the mechanism of Semen Strychni in treating amyotrophic lateral sclerosis based on network pharmacology
title_fullStr Exploring the mechanism of Semen Strychni in treating amyotrophic lateral sclerosis based on network pharmacology
title_full_unstemmed Exploring the mechanism of Semen Strychni in treating amyotrophic lateral sclerosis based on network pharmacology
title_short Exploring the mechanism of Semen Strychni in treating amyotrophic lateral sclerosis based on network pharmacology
title_sort exploring the mechanism of semen strychni in treating amyotrophic lateral sclerosis based on network pharmacology
topic Research Article: Observational Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10489316/
https://www.ncbi.nlm.nih.gov/pubmed/37682161
http://dx.doi.org/10.1097/MD.0000000000035101
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