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Potential Serotonin 5-HT2A Receptor Agonist of Psychoactive Components of Silene undulata Aiton: LC-MS/MS, ADMET, and Molecular Docking Studies.

Maram B Alhawarri, Suleiman Olimat

Current Pharmaceutical Biotechnology January 1, 2025 DOI: 10.2174/0113892010299804240324140017 (opens in new tab) via PubMed

Summary

AI-generated from the abstract

An extract of the plant Silene undulata, traditionally used to induce vivid dreams, contains 51 phytochemicals including the β-carboline alkaloids norharman, harmalol, harmaline, harmine, and ibogaine. Computer simulations predicted that harmaline, harmalol, and ibogaine bind to the serotonin 5-HT2A receptor with affinities comparable to LSD, suggesting they may act as agonists. The compounds also showed favorable predicted pharmacokinetic properties. These results support the plant's historical psychoactive use and point to potential therapeutic applications, though further research is needed.

Study at a glance

Characteristics Experimental study with computational analysis Peer reviewed
Keywords Admet. Lc-ms/ms Silene undulata Chemical profiling Molecular docking
Citations 10
Key finding The β-carboline alkaloids harmaline, harmalol, and ibogaine from Silene undulata show predicted binding affinities to the serotonin 5-HT2A receptor comparable to LSD, supporting the plant's traditional use as a dream-inducing psychoactive agent.

Abstract

Silene undulata is historically used for inducing vivid and prophetic lucid dreams, but limited information exists on its phytochemical composition and potential pharmacological properties. This study aimed to investigate the phytochemical composition of S. undulata through LC-MS/MS analysis and explore its potential serotonergic activity, which could support and confirm the traditional use of S. undulata as a dream-inducing plant. LC-MS/MS analysis was conducted on S. undulata extract, identifying 51 phytochemicals, including norharman, harmalol, harmaline, harmine, and ibogaine alkaloids. ADMET and Molecular docking investigations were employed to assess the serotonergic potential of these compounds. The analysis revealed the presence of β-carboline alkaloids, such as norharman, harmalol, harmaline, harmine, and ibogaine, within S. undulata extract. ADMET analysis showed that these compounds have a favourable pharmacokinetic properties. In addition, molecular docking investigations showed that harmaline (-8.90 Kcal/mol), harmalol (-8.56 Kcal/mol), and ibogaine (-8.75 Kcal/mol) exhibited binding affinities comparable to the control molecule, LSD (-9.14 Kcal/mol), indicating potential agonistic activity at serotonin 5-HT2A receptor. These findings provide insights into the potential therapeutic benefits of S. undulata, supporting its traditional use as a psychoactive plant. This study investigated the chemical constituents and potential serotonergic agonist activity of S. undulata for the first time. While promising, further research is necessary to uncover additional medicinal properties associated with the identified phytochemical components.

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