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Network pharmacology and metabolomics analysis of Tinospora cordifolia reveals BACE1 and MAOB as potential therapeutic targets for neuroprotection in Alzheimer’s disease

Title: Network pharmacology and metabolomics analysis of Tinospora cordifolia reveals BACE1 and MAOB as potential therapeutic targets for neuroprotection in Alzheimer’s disease
Authors: S. Amrutha; Chandran S. Abhinand; Shubham Sukerndeo Upadhyay; Ravishankar Parvaje; Thottethodi Subrahmanya Keshava Prasad; Prashant Kumar Modi
Source: Scientific Reports, Vol 15, Iss 1, Pp 1-23 (2025)
Publisher Information: Nature Portfolio, 2025.
Publication Year: 2025
Collection: LCC:Medicine; LCC:Science
Subject Terms: Tinospora cordifolia; Medhya rasayana; Untargeted metabolomics; Neuroprotection; Therapeutic targets; Medicine; Science
Description: Abstract Tinospora cordifolia has been used for thousands of years to treat various health conditions, including neurodegenerative diseases. The study aimed to elucidate the mechanism of action and protein targets of T. cordifolia in the context of Alzheimer’s disease through untargeted metabolomics and network pharmacology. LC–MS/MS analysis resulted in 1186 metabolites, including known bioactive compounds such as liquiritin, Plastoquinone 3, and Shoyuflavone A, to name a few. The network pharmacology analysis highlighted the metabolite-protein interaction with the enrichment of 591 human proteins, including neurotransmitter receptors and other regulatory proteins. Pathway analysis highlighted the enrichment of cAMP, mTOR, MAPK, and PI3K-Akt signaling pathways along with cholinergic, dopaminergic, serotonergic, glutamatergic synapse, and apoptosis. The docking results suggest that T. cordifolia metabolites could interact with key Alzheimer’s disease targets BACE1 and MAO-B, suggesting its role in neuroprotection. These findings provide insights into the biochemical pathways underlying T. cordifolia’s therapeutic effects and provides a foundation for future exploration of T. cordifolia in the context of translational research.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2045-2322
Relation: https://doaj.org/toc/2045-2322
DOI: 10.1038/s41598-025-92756-5
Access URL: https://doaj.org/article/e7d509bcefde43eb8f7a93cdeb6ef8a4
Accession Number: edsdoj.7d509bcefde43eb8f7a93cdeb6ef8a4
Database: Directory of Open Access Journals