Probing the Molecular Mechanisms of Kratom's Antipsychotic Effects through a Multi-modal Computational Approach.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Current pharmaceutical design Pub Date : 2025-01-01 DOI:10.2174/0113816128335217241031033104
Supra Wimbarti, Trina Ekawati Tallei, B H Ralph Kairupan, Nova Hellen Kapantow, Dewi Ekatanti, Rizka Fatriani, Wisnu Ananta Kusuma, Fatimawali -, Ismail Celik
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Abstract

Background: Psychosis, marked by detachment from reality, includes symptoms like hallucinations and delusions. Traditional herbal remedies like kratom are gaining attention for psychiatric conditions. This was aimed at comprehending the molecular mechanisms of Kratom's antipsychotic effects utilizing a multi-modal computational approach.

Materials and methods: This study employed network pharmacology followed by molecular docking and molecular dynamics simulation study to investigate the potential antipsychotic properties of kratom compounds by identifying their key molecular targets and interactions.

Results: Compounds present in kratom interact with a variety of receptors and proteins that play a pivotal role in neurotransmission, neurodevelopment, and cellular signaling. These interactions, particularly with dopamine and serotonin receptors, various proteins, and pathways, suggest a complex influence on psychiatric conditions. Both mitragynine and zotepine (an atypical antipsychotic drug) display significant binding affinities for 5HTR2A receptors, suggesting their potential for modulating related physiological pathways. Mitragynine displayed higher flexibility in binding compared to zotepine, which showed a more stable interaction. Hydrogen bond analysis revealed a more variable interaction profile for mitragynine than zotepine.

Conclusion: The research findings suggest that the interaction between kratom compounds and essential brain receptors could influence psychiatric conditions. Notably, both mitragynine (a key kratom component) and zotepine (an antipsychotic) bind to the 5HTR2A receptor, suggesting the potential for kratom to modulate similar pathways. Interestingly, mitragynine's flexible binding mode compared to zotepine might indicate a more diverse range of effects. Overall, the findings suggest complex interactions between kratom and the brain's signaling system, warranting further investigation into its potential therapeutic effects.

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用多模态计算方法探讨克拉通抗精神病作用的分子机制。
背景:精神病以脱离现实为特征,包括幻觉和妄想等症状。像克拉通这样的传统草药治疗精神疾病越来越受到关注。目的是利用多模态计算方法来理解Kratom抗精神病作用的分子机制。材料与方法:本研究采用网络药理学、分子对接、分子动力学模拟研究等方法,通过鉴定克拉藤类化合物的关键分子靶点和相互作用,探讨其潜在的抗精神病作用。结果:kratom中存在的化合物与多种受体和蛋白质相互作用,在神经传递、神经发育和细胞信号传导中起关键作用。这些相互作用,特别是与多巴胺和血清素受体、各种蛋白质和途径的相互作用,表明对精神疾病有复杂的影响。米特拉吉宁和左替平(一种非典型抗精神病药物)对5HTR2A受体显示出显著的结合亲和力,表明它们可能调节相关的生理通路。与佐替平相比,米特拉金的结合灵活性更高,相互作用更稳定。氢键分析显示米特拉金的相互作用谱比左替平更可变。结论:研究结果提示,克拉通化合物与脑基本受体的相互作用可能影响精神疾病。值得注意的是,米特ragynine (kratom的关键成分)和zotepine(一种抗精神病药物)都与5HTR2A受体结合,这表明kratom可能调节类似的途径。有趣的是,与左替平相比,米特ragynine灵活的结合模式可能表明其作用范围更广。总的来说,这些发现表明kratom和大脑信号系统之间存在复杂的相互作用,值得进一步研究其潜在的治疗效果。
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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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