Skip to content

Mechanistic Insights on the Neuro-Modulatory Potential of Cannabis sativa: A Network Pharmacology- and Molecular Dynamics Simulation-Based Approach

Christina Peter, Halimat Yusuf Lukman, Nosipho Wendy S’thebe, Usman Abiola Sanni, Saheed Sabiu

Pharmacognosy Journal September 19, 2025 DOI: 10.5530/pj.2025.17.51 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Computational network pharmacology and molecular dynamics simulation study Peer reviewed
Topics Cannabis
Key points The authors report that cannabis metabolites modulate central nervous system neurotransmitter genes and receptors, with CNR1 and GRM2 as hub targets in the neuroactive ligand receptor pathway. Cholesterol and campesterol showed lower binding free energies to CNR1 than the reference antidepressant anandamide, while nerolidol bound GRM2 less strongly than anandamide. The authors interpret these stable binding interactions as suggestive of a mechanistic basis for cannabis effects on brain activity during depression and chronic use.

Abstract

Background: Although, studies have reported the use of cannabis as a temporary antidepressant and implicated its chronic use in neurological diseases, the exact mechanisms through which these happen remain elusive.Objective: This study aims to investigate the neuro-modulatory potential of cannabis as antidepressant and its role in neurological disorders Methodology: Network pharmacology and molecular dynamics simulation were employed to unveil the mechanism of cannabis as a temporary antidepressant and potential agent implicated in neurological disorders.Results: A total of 156 cannabis metabolites were retrieved from data mining.22 genes were common in cannabis metabolites and central nervous system (CNS) neurotransmitters' genes.Glutamate receptor activity and neuroactive ligand receptor activity (NALR) were the most enriched biological process and signalling pathway, respectively, with cannabinoid receptor 1 (CNR1) and glutamate metabotropic receptor 2 (GRM2) being the hub targets in the NALR pathway.A probe into the structural stability of top-ranked metabolites identified cholesterol-CNR1 (-73.88 kcal/mol) and campesterol-CNR1 (-65.96kcal/mol) with lower free binding energy than reference antidepressant drug (anandamide) (-65.08 kcal/mol), whereas for GRM2, the binding free energy of nerolidol (-43.57kcal/mol) which was the least among the top ranked metabolites was higher compared to anandamide (-58.78 kcal/mol).Conclusion: Data from this study shows that the profiled cannabis metabolites displayed modulatory effects on key neurotransmitters of the CNS and their receptors and formed stable binding interaction with genes implicated in brain functioning suggestive of the mechanistic effect of cannabis on brain activity during depression and chronic use.

Citations in the library

Explore topics