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中国精品科技期刊2020
武万兴,段志辉,薛璃轩,等. 基于网络药理学研究灵芝-西洋参-冬虫夏草复方增强免疫力活性及作用机制[J]. 食品工业科技,2023,44(8):392−404. doi: 10.13386/j.issn1002-0306.2022060329.
引用本文: 武万兴,段志辉,薛璃轩,等. 基于网络药理学研究灵芝-西洋参-冬虫夏草复方增强免疫力活性及作用机制[J]. 食品工业科技,2023,44(8):392−404. doi: 10.13386/j.issn1002-0306.2022060329.
WU Wanxing, DUAN Zhihui, XUE Lixuan, et al. Immunity Enhancement Activity and Mechanism of Ganoderma lucidum-Panax quiquefolium L.-Cordyceps sinensis compound Based on Network Pharmacology[J]. Science and Technology of Food Industry, 2023, 44(8): 392−404. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022060329.
Citation: WU Wanxing, DUAN Zhihui, XUE Lixuan, et al. Immunity Enhancement Activity and Mechanism of Ganoderma lucidum-Panax quiquefolium L.-Cordyceps sinensis compound Based on Network Pharmacology[J]. Science and Technology of Food Industry, 2023, 44(8): 392−404. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022060329.

基于网络药理学研究灵芝-西洋参-冬虫夏草复方增强免疫力活性及作用机制

Immunity Enhancement Activity and Mechanism of Ganoderma lucidum-Panax quiquefolium L.-Cordyceps sinensis compound Based on Network Pharmacology

  • 摘要: 本研究系统评价了灵芝西洋参冬虫夏草复方(以下简称“复方”)的增强免疫力功能,并采用网络药理学探究其作用机制。分别考察复方的NK细胞活性、迟发型变态反应、脾淋巴细胞增殖能力和单核-巨噬细胞吞噬能力以评估其增强免疫力活性。体外和体内结果表明:复方低、中、高剂量组(0.4、0.8、2.4 g/kg)均可以显著增加NK细胞活性(P<0.001),中、高剂量组均能显著增加迟发型变态反应(P<0.001),低剂量组可以显著增加巨噬细胞吞噬能力(P<0.05)。利用多个在线数据库收集复方的活性成分、作用靶点及疾病靶点。使用Cytoscape、STRING 等软件构建复方-靶点-疾病网络与蛋白质相互作用网络,并运用Metascape对靶点基因进行GO与KEGG富集分析。网络药理学分析结果表明:该复方通过花生四烯酸、过氧麦角甾醇、胆固醇棕榈酸酯、PQ-2、环氧灵芝醇C、麦角甾-7,9,22-三烯-3-醇、麦角甾烷-7,22-二烯-3β-醇等活性物质,作用于NK细胞和T细胞的蛋白激酶B(AKT1)、表皮生长因子受体(EGFR)、非受体酪氨酸激酶(SRC)等靶点,调控肿瘤、FOXO、Th17、NK细胞等信号通路协同发挥增强免疫力作用。同时本研究初步揭示了复方增强免疫力的多组分、多靶点、多通路的协同作用机制,为后续深入研究其分子机制和应用提供了新思路和理论依据。

     

    Abstract: In this study, the immunity enhancement activity of Ganoderma lucidum-Cordyceps sinensis-Panax quiquefolium L. compound (here in after referred to as "compound") was systematically evaluated, and its mechanism was explored by network pharmacology. The NK cell activity, delayed allergic reaction, spleen lymphocyte proliferation and monocyte-macrophage phagocytosis of compound were investigated to evaluate its immunity enhancement activity. The results in vivo and in vitro indicated the low, medium and high dose groups (0.4, 0.8, 2.4 g/kg) of compound could significantly increase NK cell activity (P<0.001), the medium and high dose groups could significantly increase the delayed allergic reaction activity (P<0.001), and the low dose group could significantly increase the phagocytic index of monocyte-macrophage (P<0.05). The active ingredients, action targets and disease targets of the compound were collected by multiple online databases and document retrieval. Cytoscape and STRING were utilized to construct the interaction network between compound-target-disease network and protein, GO and KEGG enrichment analysis of target genes performed by Metascape. The results of network pharmacological analysis indicated that the compound could act on 94 targets such as protein kinase B (AKT1), epidermal growth factor receptor (EGFR) and non-receptor tyrosine kinase (SRC) of NK cells and T cells by active substances such as arachidonic acid, peroxyergosterol, cholesterol palmitate, PQ-2, epoxy ganoderma alcohol C, ergosterol-7,9,22-triene-3-alcohol, ergosteran-7,22-diene-3β-alcohol and other active compounds, regulate 1382 GO items, including tumor regulation, FOXO, Th17 and NK cells and 171 signal channel to synergistically enhance immunity. Meanwhile, this study preliminarily revealed the synergistic mechanism of multi-components, multi-targets and multi-pathways of the compound to immunity enhancement, which could provide new ideas and theoretical basis for further study in its molecular mechanism and application.

     

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