Multifaceted Computational Approach to Explore Nardostachys Jatamansi Neuroprotective Phytochemicals as Potential MAO-B Inhibitors for Parkinson’s Disease

Publish Year: 1404
نوع سند: مقاله ژورنالی
زبان: English
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JR_CHM-9-9_005

تاریخ نمایه سازی: 30 تیر 1404

Abstract:

Parkinson’s disease is a progressive neurodegenerative disorder characterized by the loss of dopaminergic neurons and motor dysfunction, in which MAO-B plays a crucial role by catalyzing the breakdown of dopamine and generating oxidative stress. MAO-B inhibition is a well-established strategy for managing Parkinson’s disease symptoms and slowing disease progression. Given its traditional claims in Ayurvedic medicine for the treatment of neurological disorders, Nardostachys jatamansi was selected for in silico screening to explore its neuroprotective potential. A total of ۲۵ phytochemicals were evaluated using computational tools. All compounds satisfied Lipinski’s Rule of Five and Jorgensen’s Rule of Three, indicating favorable oral bioavailability and drug likeness. Molecular docking studies revealed that the phytochemicals jatamansinone (-۹.۷۲۹ kcal/mol), eselin (-۹.۱۳۸ kcal/mol), and jatamansinol (-۸.۹۷۹ kcal/mol) exhibited strong binding affinities with MAO-B, comparable to the reference inhibitor safinamide (-۱۰.۶۶ kcal/mol). These phytochemicals effectively occupied the active site, interacting with key residues such as Tyr۳۲۶, and extended into both the entrance and substrate cavities, suggesting a mechanism of inhibition similar to that of safinamide. Furthermore, ۱۰۰ ns molecular dynamics simulations demonstrated stable interactions and minimal structural changes in the MAO-B-ligand complexes throughout the simulation trajectory. Prediction of Activity Spectra for Substances (PASS) analysis predicted a wide range of neuroprotective properties of these phytochemicals, including antioxidant, anti-inflammatory, neurotransmitter-modulating, and motor-stabilizing activities. Their predicted ability to influence the serotonin and GABA pathways further highlights their potential as promising natural agents for the treatment or prevention of Parkinson’s disease and related neurodegenerative disorders.

Authors

Trupti Pratik Durgawale

Department of Pharmaceutical chemistry Krishna Institute of Pharmacy Krishna Vishwa Vidyapeeth (Deemed to be University) Karad Maharashtra ۴۱۵۵۳۹, India

Wurood A Shihab

Department of Pharmacology, Chitwaan Medical College (CMC), Gandhi Nagar, Gujarat ۳۸۲۰۱۰, India

Mohd Masih Uzzaman Khan

Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, Qassim University, Buraidah ۵۱۴۵۲, Saudi Arabia

Hassan A Madkhali

Department of Pharmacology and Toxicology, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia

Mohd Nazam Ansari

Department of Pharmacology and Toxicology, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia

Susithra Ethiraj

College of Pharmacy, University Accreditation Coordinator, Sri Venkateswaraa University, Red Hills, Chennai, Padianallur, Tamil Nadu ۶۰۰۰۶۷, India

Mirza Shahed Baig

Department of Pharmaceutical Chemistry, Y. B. Chavan College of Pharmacy, Aurangabad ۴۳۱۰۰۱, India

Thukani Sathanantham Shanmugarajan

Department of Pharmaceutics, School of Pharmaceutical Sciences, Vels Institute of Science, Technology and Advanced Studies (VISTAS). PV Vaithiyalingam Rd, Velan Nagar, Krishna Puram, Pallavaram, Chennai, ۶۰۰۱۱۷, Tamil Nadu, India

Kirti Naik

Department of Pharmacognosy, Bharati Vidyapeeth’s College of Pharmacy, Navi Mumbai, India

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