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利用ADMET分析和分子对接阐明一种含大麻草药疗法(Suk-Saiyasna)抑制乙酰胆碱酯酶的神经保护机制。

Utilizing ADMET Analysis and Molecular Docking to Elucidate the Neuroprotective Mechanisms of a Cannabis-Containing Herbal Remedy (Suk-Saiyasna) in Inhibiting Acetylcholinesterase.

作者信息

Sumontri Suwimon, Eiamart Wanna, Tadtong Sarin, Samee Weerasak

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Srinakharinwirot University, Nakhon Nayok 26120, Thailand.

Technical and Planning Division, Department of Thai Traditional and Alternative Medicine, Ministry of Public Health, Nonthaburi 11000, Thailand.

出版信息

Int J Mol Sci. 2025 Mar 29;26(7):3189. doi: 10.3390/ijms26073189.

Abstract

Alzheimer's disease is characterized by the degeneration of cholinergic neurons, which is primarily driven by the acetylcholinesterase (AChE) enzyme and oxidative stress. This study investigated the therapeutic potential of the cannabis-containing herbal remedy Suk-Saiyasna in alleviating amyloid β42 (Aβ42)-induced cytotoxicity in SH-SY5Y cells. The DPPH radical-scavenging activity and inhibitory effects on AChE were evaluated in vitro. The AChE inhibitory potential of 167 ligands, including cannabinoids, flavonoids, terpenoids, and alkaloids derived from Suk-Saiyasna, was assessed using ADMET analysis and molecular docking techniques. The results demonstrated that the Suk-Saiyasna extract exhibited a DPPH radical scavenging effect with an IC value of 27.40 ± 1.15 µg/mL and notable AChE inhibitory activity with an IC of 1.25 ± 0.35 mg/mL. Importantly, at a concentration of 1 µg/mL, the extract significantly protected cells from Aβ42-induced stress compared to controls. Docking studies revealed that delta-9-tetrahydrocannabinol (Δ-THC), mesuaferrone B, piperine, β-sitosterol, and chlorogenic acid exhibited substantial binding affinities to AChE, surpassing reference drugs like galantamine and rivastigmine. Furthermore, in silico ADMET predictions indicated that Δ-THC and piperine possessed favorable pharmacokinetic profiles, including solubility, absorption, and blood-brain barrier permeability, with no neurotoxicity or carcinogenicity associated with Δ-THC.

摘要

阿尔茨海默病的特征是胆碱能神经元退化,这主要由乙酰胆碱酯酶(AChE)和氧化应激驱动。本研究调查了含大麻草药疗法Suk-Saiyasna在减轻淀粉样β42(Aβ42)诱导的SH-SY5Y细胞毒性方面的治疗潜力。体外评估了其对DPPH自由基的清除活性和对AChE的抑制作用。使用ADMET分析和分子对接技术评估了167种配体(包括源自Suk-Saiyasna的大麻素、黄酮类化合物、萜类化合物和生物碱)的AChE抑制潜力。结果表明,Suk-Saiyasna提取物表现出DPPH自由基清除作用,IC值为27.40±1.15μg/mL,并且具有显著的AChE抑制活性,IC为1.25±0.35mg/mL。重要的是,在浓度为1μg/mL时,与对照组相比,该提取物能显著保护细胞免受Aβ42诱导的应激。对接研究表明,δ-9-四氢大麻酚(Δ-THC)、铁力木酮B、胡椒碱、β-谷甾醇和绿原酸与AChE表现出很强的结合亲和力,超过了加兰他敏和卡巴拉汀等参考药物。此外,计算机辅助ADMET预测表明,Δ-THC和胡椒碱具有良好的药代动力学特征,包括溶解性、吸收性和血脑屏障通透性,且Δ-THC无神经毒性或致癌性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4120/11989231/2fe1e02c4bc8/ijms-26-03189-g001.jpg

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