Investigating the Potential Anti-Alzheimer’s Disease Mechanism of Marine Polyphenols: Insights from Network Pharmacology and Molecular Docking

• Published in: Marine drugs 2023-11, Vol.21 (11), p.580
• Main Authors: Youn, Kumju, Ho, Chi-Tang, Jun, Mira
• Format: Article
• Language: English
• Subjects: 8,8′-bieckol; AKT1 protein; Algae; Alzheimer's disease; Care and treatment; Dementia; dieckol; Disease prevention; eckol; Encyclopaedias; Encyclopedias; Enzymes; Epidermal growth factor receptors; ESR1 protein; Genes; Genomes; Health aspects; Kinases; MAP kinase; marine polyphenols; Marine resources; Molecular docking; network pharmacology; Neurodegenerative diseases; Ontology; Pharmacology; Phosphorylation; Physiological aspects; Plasma; Polyphenols; Protein-tyrosine kinase; Proteins; Rap1 protein; Tyrosine
• ISSN: 1660-3397; 1660-3397
• DOI: 10.3390/md21110580

Marine polyphenols, including eckol(EK), dieckol(DK), and 8,8’-bieckol(BK), have attracted attention as bioactive ingredients for preventing Alzheimer’s disease (AD). Since AD is a multifactorial disorder, the present study aims to provide an unbiased elucidation of unexplored targets of AD mechanisms and a systematic prediction of effective preventive combinations of marine polyphenols. Based on the omics data between each compound and AD, a protein–protein interaction (PPI) network was constructed to predict potential hub genes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed to provide further biological insights. In the PPI network of the top 10 hub genes, AKT1, SRC, EGFR, and ESR1 were common targets of EK and BK, whereas PTGS2 was a common target of DK and BK. GO and KEGG pathway analysis revealed that the overlapped genes between each compound and AD were mainly enriched in EGFR tyrosine kinase inhibitor resistance, the MAPK pathway, and the Rap1 and Ras pathways. Finally, docking validation showed stable binding between marine polyphenols and their top hub gene via the lowest binding energy and multiple interactions. The results expanded potential mechanisms and novel targets for AD, and also provided a system-level insight into the molecular targets of marine polyphenols against AD.