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基于网络药理学探讨淫羊藿苷通过 BDNF-TrkB 通路治疗抑郁症的作用机制。

Exploring the mechanism of Icariin in the treatment of depression through BDNF-TrkB pathway based on network pharmacology.

机构信息

School of Pharmacy, North China University of Science and Technology, Tangshan, 063210, Hebei Province, China.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2024 Jan;397(1):463-478. doi: 10.1007/s00210-023-02615-1. Epub 2023 Jul 20.

Abstract

Depression has increasingly become a disease that seriously harms people's mental health around the world. Icariin is the main active component of Epimedii Herba and effective on protecting the central nervous system. The purpose of this study was to explore the mechanism of icariin against depression based on network pharmacology and molecular docking. The potential targets related to icariin and depression were obtained by accessing network databases. The Metascape database was used for the enrichment analysis of GO function and KEGG pathways. A common target-pathway network was constructed using Cytoscape 3.9.0 software. Schrödinger Maestro 12.8 was adopted to evaluate the binding ability of icariin to core targets. Mice were induced by the chronic unpredictable mild stress (CUMS) model, and the prediction results of this study were verified by in vivo experiments. A total of 109 and 3294 targets were identified in icariin and depression, respectively. The common target-pathway network was constructed, and 7 core target genes were obtained. The molecular docking results of the 7 core target genes with icariin showed good affinity. In a CUMS-induced depression model, we found that icariin could effectively improve depression-like behavior of mice, increase the expression of monoamine neurotransmitters 5-hydroxytryptamine, dopamine, and norepinephrine, decrease the secretion of inflammatory factors tumor necrosis factor-α, interleukin-6, and interleukin-1β, and upregulate the relative expression levels of BDNF, p-TrkB/TrkB, p-Akt/Akt, p-CREB/CREB, MAPK3, MAPK1, Bcl-2, EGFR, and mTOR. The results suggest that icariin has certain antidepressant effects, and may be mediated by the BDNF-TrkB signaling pathway. It provides new ideas for the treatment of depression in the future.

摘要

抑郁症日益成为一种严重危害全球人类精神健康的疾病。淫羊藿苷是淫羊藿的主要活性成分,具有保护中枢神经系统的作用。本研究旨在基于网络药理学和分子对接探讨淫羊藿苷抗抑郁的作用机制。通过访问网络数据库获得与淫羊藿苷和抑郁症相关的潜在靶点。使用 Metascape 数据库对 GO 功能和 KEGG 通路进行富集分析。使用 Cytoscape 3.9.0 软件构建共同靶点-通路网络。采用 Schrödinger Maestro 12.8 评估淫羊藿苷与核心靶点的结合能力。采用慢性不可预知性温和应激(CUMS)模型诱导小鼠,并通过体内实验验证本研究的预测结果。共鉴定出淫羊藿苷 109 个和抑郁症 3294 个靶标。构建共同靶点-通路网络,获得 7 个核心靶标基因。7 个核心靶基因与淫羊藿苷的分子对接结果显示出良好的亲和力。在 CUMS 诱导的抑郁模型中,我们发现淫羊藿苷能有效改善小鼠的抑郁样行为,增加 5-羟色胺、多巴胺和去甲肾上腺素等单胺神经递质的表达,减少肿瘤坏死因子-α、白细胞介素-6 和白细胞介素-1β等炎症因子的分泌,并上调 BDNF、p-TrkB/TrkB、p-Akt/Akt、p-CREB/CREB、MAPK3、MAPK1、Bcl-2、EGFR 和 mTOR 的相对表达水平。结果表明,淫羊藿苷具有一定的抗抑郁作用,可能通过 BDNF-TrkB 信号通路介导。为今后抑郁症的治疗提供了新的思路。

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