Unveiling Neuroprotective Potential of Spice Plant-Derived Compounds against Alzheimer’s Disease: Insights from Computational Studies

• Published in: International journal of alzheimer's disease 2023-09, Vol.2023, p.1-19
• Main Authors: Alom, Md. Murshid, Bonna, Rejwana Parvin, Islam, Ariful, Alom, Md. Wasim, Rahman, Md. Ekhtiar, Faruqe, Md Omar, Khalekuzzaman, Md, Zaman, Rashed, Islam, Md. Asadul
• Format: Article
• Language: English
• Subjects: Acetylcholinesterase; Advertising executives; Alzheimer's disease; Analysis; Binding energy; Brain research; Clinical trials; Cognitive ability; Computational neuroscience; Computer simulation; Dementia; Donepezil; Force and energy; Free energy; Global health; Hydrogen; Hydrogen bonds; Inhibitors; Ligands; Mathematical analysis; Medical research; Medicine, Experimental; Memory; Molecular dynamics; Neurodegenerative diseases; Neuroprotection; Pharmacokinetics; Phytochemicals; Plants; Principal components analysis; Protein binding; Proteins; Public health; Quercetin; Simulation; Simulation methods; Software; Surface area
• ISSN: 2090-8024; 2090-0252; 2090-0252
• DOI: 10.1155/2023/8877757

Alzheimer’s disease (AD) is a serious threat to the global health care system and is brought on by a series of factors that cause neuronal dysfunction and impairment in memory and cognitive decline. This study investigated the therapeutic potential of phytochemicals that belong to the ten regularly used spice plants, based on their binding affinity with AD-associated proteins. Comprehensive docking studies were performed using AutoDock Vina in PyRx followed by molecular dynamic (MD) simulations using AMBER 14. The docking study of the chosen molecules revealed the binding energies of their interactions with the target proteins, while MD simulations were carried out to verify the steadiness of bound complexes. Through the Lipinski filter and admetSAR analysis, the chosen compounds’ pharmacokinetic characteristics and drug likeness were also examined. The pharmacophore mapping study was also done and analyzed for best selected molecules. Additionally, principal component analysis (PCA) was used to examine how the general motion of the protein changed. The results showed quercetin and myricetin to be potential inhibitors of AChE and alpha-amyrin and beta-chlorogenin to be potential inhibitors of BuChE, exhibiting best binding energies comparable to those of donepezil, used as a positive control. The multiple descriptors from the simulation study, root mean square deviation (RMSD), root mean square fluctuation (RMSF), hydrogen bond, radius of gyration (Rg), and solvent-accessible surface areas (SASA), confirm the stable nature of the protein-ligand complexes. Molecular mechanic Poisson-Boltzmann surface area (MM-PBSA) binding free energy calculations indicated the energetically favorable binding of the ligands to the protein. Finally, according to pharmacokinetic properties and drug likeness, characteristics showed that quercetin and myricetin for AChE and alpha-amyrin and beta-chlorogenin for BuChE were found to be the most effective agents for treating the AD.