Exploring Cannabis sativa L for Anti-Alzheimer Potential: An Extensive Computational Study including Molecular Docking, Molecular Dynamics, and ADMET Assessments.

IF 1.9 4区 医学 Q3 CHEMISTRY, MEDICINAL
Hassan Nour, Imane Yamari, Oussama Abchir, Nouh Mounadi, Abdelouahid Samadi, Salah Belaidi, Samir Chtita
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引用次数: 0

Abstract

Introduction: Cholinesterase enzymes play a pivotal role in hydrolyzing acetylcholine, a neurotransmitter crucial for memory and cognition, into its components, acetic acid, and choline. A primary approach in addressing Alzheimer's disease symptoms is by inhibiting the action of these enzymes.

Methods: With this context, our study embarked on a mission to pinpoint potential Cholinesterase (ChE) inhibitors using a comprehensive computational methodology. A total of 49 phytoconstituents derived from Cannabis sativa L underwent in silico screening via molecular docking, pharmacokinetic and pharmacotoxicological analysis, to evaluate their ability to inhibit cholinesterase enzymes. Out of these, two specific compounds, namely tetrahydrocannabivarin and Δ-9- tetrahydrocannabinol, belonging to cannabinoids, stood out as prospective therapeutic agents against Alzheimer's due to their potential as cholinesterase inhibitors. These candidates showcased commendable binding affinities with the cholinesterase enzymes, highlighting their interaction with essential enzymatic residues.

Results: They were predicted to exhibit greater binding affinities than Rivastigmine and Galantamine. Their ADMET assessments further classified them as viable oral pharmaceutical drugs. They are not expected to induce any mutagenic or hepatotoxic effects and cannot produce skin sensitization. In addition, these phytoconstituents are predicted to be BBB permeable and can reach the central nervous system (CNS) and exert their therapeutic effects. To delve deeper, we explored molecular dynamics (MD) simulations to examine the stability of the complex formed between the best candidate (Δ-9-tetrahydrocannabinol) and the target proteins under simulated biological conditions. The MD study affirmed that the ligand-ChE recognition is a spontaneous reaction leading to stable complexes.

Conclusion: Our research outcomes provide valuable insights, offering a clear direction for the pharmaceutical sector in the pursuit of effective anti-Alzheimer treatments.

探索大麻L抗阿尔茨海默病的潜力:包括分子对接,分子动力学和ADMET评估的广泛计算研究。
胆碱酯酶在乙酰胆碱水解过程中起关键作用,乙酰胆碱是一种对记忆和认知至关重要的神经递质,其成分为乙酸和胆碱。解决阿尔茨海默病症状的主要方法是抑制这些酶的作用。方法:在这种背景下,我们的研究开始了一项任务,即使用综合计算方法确定潜在的胆碱酯酶(ChE)抑制剂。通过分子对接、药代动力学和药物毒理学分析,对49种大麻植物成分进行了硅筛选,以评价其抑制胆碱酯酶的能力。其中,两种特定的化合物,即四氢大麻素和Δ-9-四氢大麻酚,属于大麻素,由于其作为胆碱酯酶抑制剂的潜力,作为治疗阿尔茨海默氏症的前瞻性药物脱颖而出。这些候选物显示出与胆碱酯酶的良好结合亲和力,突出了它们与必需酶残基的相互作用。结果:预测它们比利瓦斯汀和加兰他明具有更强的结合亲和力。它们的ADMET评估进一步将它们归类为可行的口服药物。它们不会引起任何诱变或肝毒性作用,也不会产生皮肤致敏。此外,这些植物成分被预测为血脑屏障可渗透,可到达中枢神经系统(CNS)并发挥其治疗作用。为了深入研究,我们探索了分子动力学(MD)模拟,以检查在模拟生物条件下最佳候选蛋白(Δ-9-tetrahydrocannabinol)和目标蛋白之间形成的复合物的稳定性。MD研究证实配体- che识别是一个自发反应,导致稳定的配合物。结论:我们的研究结果提供了有价值的见解,为制药行业寻求有效的抗阿尔茨海默病治疗提供了明确的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicinal Chemistry
Medicinal Chemistry 医学-医药化学
CiteScore
4.30
自引率
4.30%
发文量
109
审稿时长
12 months
期刊介绍: Aims & Scope Medicinal Chemistry a peer-reviewed journal, aims to cover all the latest outstanding developments in medicinal chemistry and rational drug design. The journal publishes original research, mini-review articles and guest edited thematic issues covering recent research and developments in the field. Articles are published rapidly by taking full advantage of Internet technology for both the submission and peer review of manuscripts. Medicinal Chemistry is an essential journal for all involved in drug design and discovery.
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