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揭示睡茄对神经元细胞结构和突触发生的影响:体外联合网络药理学方法。

Unveiling the effect of Withania somnifera on neuronal cytoarchitecture and synaptogenesis: A combined in vitro and network pharmacology approach.

机构信息

Department of Anatomy, Dongguk University College of Medicine, Gyeongju, Republic of Korea.

Department of Pharmacy, BGC Trust University Bangladesh, Chittagong, Bangladesh.

出版信息

Phytother Res. 2022 Jun;36(6):2524-2541. doi: 10.1002/ptr.7466. Epub 2022 Apr 20.

DOI:10.1002/ptr.7466
PMID:35443091
Abstract

Withania somnifera (WS), is known for its remarkable contribution in herbal medicine and Ayurveda, which is therapeutically applied to improve memory and anxiety in patients. However, the pharmacological details of this plant on memory boosting yet remained undefined. This study provides mechanistic insights on the effect of ethanol solution extract of the whole plant of WS (WSEE) on neuritogenesis by combining in vitro and in silico network pharmacology approaches. WSEE promoted significant neuronal growth through early differentiation, axodendritic arborization, and synaptogenesis on primary hippocampal neurons. The network pharmacological study confirmed that the neuritogenic activity is potentially mediated by modulating the neurotrophin signaling pathway, where NRTK1 (TrkA) was revealed as the primary target of WS secondary metabolites. This neurotrophic activity of WSEE was significantly stifled by the presence of TrkA inhibitor, which further confirms the TrkA-dependent activity of WSEE. In addition, a molecular docking study suggested steroidal lactones present in the WS might act as nerve growth factor (NGF)-mimetics, activating TrkA by binding to the NGF-binding domain. As a whole, the findings of the study suggest a significant role of WSEE on neuritogenesis and its potential to function as a therapeutic agent and in drug designing for the prevention and treatment of memory-related neurological disorders.

摘要

睡茄(Withania somnifera,WS)以其在草药学和阿育吠陀医学中的卓越贡献而闻名,被广泛应用于改善患者的记忆力和焦虑症。然而,这种植物在增强记忆力方面的药理学细节尚未明确。本研究通过结合体外和基于网络的药理学方法,提供了关于 WS 全株乙醇溶液提取物(WSEE)在神经突生成方面的作用的机制见解。WSEE 通过在原代海马神经元上的早期分化、轴突树突分支和突触发生,促进了显著的神经元生长。网络药理学研究证实,神经突生成活性可能是通过调节神经营养因子信号通路来介导的,其中 NRTK1(TrkA)被揭示为 WS 次生代谢物的主要靶点。WSEE 的这种神经营养活性被 TrkA 抑制剂的存在显著抑制,这进一步证实了 WSEE 的 TrkA 依赖性活性。此外,分子对接研究表明,WS 中存在的甾体内酯可能作为神经生长因子(NGF)类似物,通过与 NGF 结合域结合来激活 TrkA。总的来说,该研究的结果表明 WSEE 在神经突生成中的重要作用及其作为治疗剂和药物设计用于预防和治疗与记忆相关的神经紊乱的潜力。

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