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Multi-modal neuroprotection of L. against Alzheimer's disease: and study. | LitMetric

AI Article Synopsis

  • L. is a medicinal plant being studied for its potential effects on Alzheimer's disease (AD), with a focus on its leaves and flowers, using various methanol, ethanol, and ethyl extracts.
  • Molecular docking studies identified three key phytochemicals—protoberberine, protopine, and codeine—that show strong binding affinities and the ability to target multiple enzymes involved in AD, such as AChE and BACE-1.
  • The extracts demonstrated promising antioxidant and anti-cholinesterase activities, supporting the hypothesis of L.'s anti-AD properties, but further validation is recommended for a complete assessment.

Article Abstract

L. is a medicinal plant, but its impact on Alzheimer's disease (AD) is right now undetermined. We intended to investigate the in-vitro anti-AD potential of leaves and flowers of methanol, ethanol, and ethyl extracts and to identify multi-modal anti-AD phytochemicals by computational approaches. Molecular docking of 196 phytochemicals identified three hit phytochemicals (protoberberine, protopine, and codeine) with higher binding affinity and multi-targeting ability toward AChE, BChE, BACE-1, and GSK-3β. Further MM-GBSA assays confirmed the integrity of these phytochemicals as the hit phytochemicals. However, these phytochemicals demonstrated favorable pharmacokinetics (PK) and drugable properties having no toxicity. Molecular dynamics simulations confirmed the binding strength of the hit phytoconstituents in the active pockets of AChE, BChE, BACE-1, and GSK-3β with multi-targeting inhibitory activities. All the extracts exhibited dose-dependent antioxidant and anti-cholinesterase activities supporting the results in the context of oxidative stress and cholinergic pathways. Our results offer scientific validation of the anti-AD properties of L. and identified protoberberine, protopine, and codeine that could be used for the development of multi-modal inhibitors of AChE, BChE, BACE-1, and GSK-3β to combat AD. Additional validation is recommended to ensure a thorough assessment in the present research.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11402773PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e37178DOI Listing

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