Guang'anmen Hospital, China Academy of Chinese Medicine Sciences, Beijing, China.
PLoS One. 2024 Nov 19;19(11):e0310960. doi: 10.1371/journal.pone.0310960. eCollection 2024.
The 5-hydroxytryptamine (5-HT) and dopamine (DA) receptors have emerged as significant targets for therapeutic intervention in psychiatric disorders. Currently, the efficacy of psychiatric drugs is limited by challenges in achieving desired outcomes, the occurrence of adverse effects, dependence, and withdrawal reactions. Consequently, there is a pressing need for the development of safe and effective therapeutic agents for psychiatric disorders. To explore the potential effects of natural product extracts as therapeutic agents for psychiatric disorders, 73 active ingredients from natural medicine extracts were screened to identify potential inhibitors of the serotonin 2A receptor (5-HT2AR) and dopamine D2 receptor (DRD2) using computerized virtual molecular docking. The most effective inhibitor of 5-HT2AR and DRD2 among these natural extracts was then evaluated for its drug-like properties using ADMET analysis, and its mechanisms of antagonism on DRD2 and 5-HT2AR were studied through molecular dynamics simulation. Risperidone was used as a positive control drug. The results showed that ruscogenin (RUS) was the most effective inhibitor of 5-HT2AR and DRD2, possessing favorable drug-like properties (most values of ADMET analysis were within the optimal range). When compared to risperidone, RUS exhibited more stable root mean square deviation (RMSD) plots, lower root mean square fluctuation (RMSF) values from residues 50 to 260, stronger hydrogen bonding interactions, higher compactness, a smaller solvent-accessible surface area (SASA) value, and lower binding free energy (-43.81 kcal/mol vs. -35.68 kcal/mol). RUS also demonstrated inhibitory effects on DRD2, as indicated by stable RMSD plots, low RMSF values from residues 50 to 250, strong hydrogen bonding interactions, high compactness, a small SASA value, and low binding free energy (-35.00 kcal/mol). Consequently, this research suggests that RUS, a natural pharmaceutical extract, is a promising candidate for further validation through clinical studies, representing a potential development of a therapeutic agent targeting psychiatric disorders.
5-羟色胺(5-HT)和多巴胺(DA)受体已成为治疗精神疾病的重要靶点。目前,精神药物的疗效受到实现预期效果、产生不良反应、依赖性和戒断反应等挑战的限制。因此,迫切需要开发安全有效的精神疾病治疗药物。为了探索天然产物提取物作为精神疾病治疗药物的潜在作用,使用计算机虚拟分子对接筛选了 73 种天然药物提取物中的活性成分,以鉴定潜在的 5-羟色胺 2A 受体(5-HT2AR)和多巴胺 D2 受体(DRD2)抑制剂。然后,使用 ADMET 分析评估这些天然提取物中对 5-HT2AR 和 DRD2 抑制作用最强的化合物的类药性,并通过分子动力学模拟研究其对 DRD2 和 5-HT2AR 的拮抗机制。利培酮被用作阳性对照药物。结果表明,榕树根素(RUS)是对 5-HT2AR 和 DRD2 抑制作用最强的化合物,具有良好的类药性(ADMET 分析的大多数值均在最佳范围内)。与利培酮相比,RUS 的均方根偏差(RMSD)图更稳定,残基 50 到 260 之间的均方根波动(RMSF)值更低,氢键相互作用更强,紧凑性更高,溶剂可及表面积(SASA)值更小,结合自由能更低(-43.81 kcal/mol 对-35.68 kcal/mol)。RUS 对 DRD2 也具有抑制作用,表现为 RMSD 图稳定,残基 50 到 250 之间的 RMSF 值低,氢键相互作用强,紧凑性高,SASA 值小,结合自由能低(-35.00 kcal/mol)。因此,这项研究表明,榕树根素,一种天然药物提取物,是通过临床研究进一步验证的有前途的候选药物,代表了一种针对精神疾病的治疗药物的潜在发展。