针灸治疗原发性抑郁症的核心穴位研究:结合数据挖掘和网络针灸学分析

Unveiling core acupoints in acupuncture treatment for primary depressive disorder: integrating data mining and network acupuncture-based analysis

  • 摘要:
    目的 通过数据挖掘和网络分析,识别针灸治疗原发性抑郁障碍(PDD)的核心穴位处方并阐明其分子机制。
    方法 系统检索PubMed、Embase、Ovid Technologies、Web of Science、Cochrane Library、中国知网、维普数据库、万方数据库和中国生物医学文献服务系统自建库至2025年1月31日发表的针灸治疗PDD的临床研究文献。采用描述性统计、高频穴位分析、度与介数中心性分析及核心穴位处方挖掘以确定PDD治疗的优势配伍。通过网络针灸学预测核心穴位处方的治疗靶点。进行蛋白质-蛋白质相互作用(PPI)网络与分子复合物检测(MCODE)分析以确定关键靶点和功能模块。通过基因本体(GO)和京都基因与基因组百科全书(KEGG)通路分析探究核心穴位处方治疗PDD的潜在生物学机制。
    结果 分析共纳入了57个穴位处方。核心处方包括百会(GV20)、印堂(GV29)、内关(PC6)、合谷(LI4)和神门(HT7)。网络针灸学鉴定出88个潜在治疗靶点(其中79个与PDD重叠)。PPI网络分析揭示了关键靶点,包括白细胞介素(IL)-6、IL-1β、肿瘤坏死因子(TNF)-α、Toll样受体4(TLR4)、IL-10、脑源性神经营养因子(BDNF)、转化生长因子(TGF)-β1、C-X-C基序趋化因子配体10(CXCL10)、丝裂原活化蛋白激酶3(MAPK3)和一氧化氮合酶1(NOS1)。MCODE模块分析识别出三个功能一致的簇:炎症-稳态(评分为6.571)、可塑性-神经传递(评分为3.143)和氧化应激(评分为3.000)。GO和KEGG富集分析表明,主要通路涉及MAPK、磷酸肌醇3-激酶/蛋白激酶B(PI3K/Akt)和缺氧诱导因子(HIF)-1等,提示其作用机制涉及神经炎症调节、神经可塑性恢复以及免疫-氧化应激稳态的调控。
    结论 本研究揭示了针灸通过多层次作用机制缓解抑郁症状,主要涉及抑制神经炎症、增强神经可塑性及调节氧化应激,系统阐明了针灸的抗抑郁作用,并为进一步的机制研究提供了新靶点。

     

    Abstract:
    Objective To identify core acupoint patterns and elucidate the molecular mechanisms of acupuncture for primary depressive disorder (PDD) through data mining and network analysis.
    Methods A comprehensive literature search was conducted across PubMed, Embase, Ovid Technologies (OVID), Web of Science, Cochrane Library, China National Knowledge Infrastructure (CNKI), China National Knowledge Infrastructure Database (VIP), Wanfang Data, and SinoMed Database from database foundation to January 31, 2025, for clinical studies on acupuncture treatment of PDD. Descriptive statistics, high-frequency acupoint analysis, degree and betweenness centrality evaluation, and core acupoint prescription mining identified predominant therapeutic combinations for PDD. Network acupuncture was used to predict therapeutic target for the core acupoint prescription. Subsequent protein-protein interaction (PPI) network and molecular complex detection (MCODE) analyses were conducted to identify the key targets and functional modules. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses explored the underlying biological mechanisms of the core acupoint prescription in treating PDD.
    Results A total of 57 acupoint prescriptions underwent systematic analysis. The core therapeutic combinations comprised Baihui (GV20), Yintang (GV29), Neiguan (PC6), Hegu (LI4), and Shenmen (HT7). Network acupuncture analysis identified 88 potential therapeutic targets (79 overlapping with PDD), while PPI network analysis revealed central regulatory nodes, including interleukin (IL)-6, IL-1β, tumor necrosis factor (TNF)-α, toll-like receptor 4 (TLR4), IL-10, brain-derived neurotrophic factor (BDNF), transforming growth factor (TGF)-β1, C-X-C motif chemokine ligand 10 (CXCL10), mitogen-activated protein kinase 3 (MAPK3), and nitric oxide synthase 1 (NOS1). MCODE-based modular analysis further elucidated three functionally coherent clusters: inflammation-homeostasis (score = 6.571), plasticity-neurotransmission (score = 3.143), and oxidative stress (score = 3.000). GO and KEGG analyses demonstrated significant enrichment of the MAPK, phosphoinositide 3-kinase/protein kinase B (PI3K/Akt), and hypoxia-inducible factor (HIF)-1 signaling pathways. These mechanistic insights suggested that the antidepressant effects mediated through mechanisms of neuroinflammatory regulation, neuroplasticity restoration, and immune-oxidative stress homeostasis.
    Conclusion This study reveals that acupuncture alleviates depression through a multi-level mechanism, primarily involving the neuroinflammation suppression, neuroplasticity enhancement, and oxidative stress regulation. These findings systematically clarify the underlying mechanisms of acupuncture’s antidepressant effects and identify novel therapeutic targets for further mechanistic research.

     

/

返回文章
返回