基于代谢组学和网络药理学的五味子 "汗浸法 "加工品镇痛机理研究

Caiyao Han, Guo Feng, Chenchen Ren, Wei Li, Wen Liu, Gang Liu, Xueli Song, Ju Zhang, Yan Lei, Zhengyan He, Tingting Liu, Kexin Ma, Jinxin Hou
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引用次数: 0

摘要

背景:RWI 具有镇痛作用,与 4-吡哆酸、l-谷氨酸和γ-氨基丁酸等代谢物有关。它参与精氨酸和脯氨酸代谢、精氨酸生物合成以及丙氨酸、天冬氨酸和谷氨酸代谢。在网络药理学中,RWI 与疼痛疾病有 404 个共同靶点,筛选出 8 个核心靶点,包括 SRC、STAT3 和 HSP90AA1。GO功能富集分析发现,RWI对蛋白质磷酸化和异生物刺激反应等分子过程、受体复合物和膜筏等细胞组成以及酶结合等分子功能都有影响。KEGG 通路富集分析获得了 193 个通路。与代谢组学分析结果相同,精氨酸脯氨酸代谢和氮代谢参与了同一条通路。目的:探讨经 "汗浸法 "处理的 RWI 的镇痛效果和治疗机制。材料与方法用醋酸进行扭转实验。利用 1H-NMR 技术对血清样本进行代谢组学分析,并通过网络药理学进行基因本体(GO)和京都基因组百科全书(KEGG)分析,筛选 RWI 与疼痛疾病的交叉靶点。结果显示RWI 具有镇痛作用,并与 4-吡哆酸、l-谷氨酸和矢车菊碱等代谢物有关。它参与精氨酸和脯氨酸代谢、精氨酸生物合成以及丙氨酸、天门冬氨酸和谷氨酸代谢。在网络药理学中,RWI 与疼痛疾病有 404 个共同靶点,筛选出 8 个核心靶点,包括 SRC、STAT3 和 HSP90AA1。GO功能富集分析发现,RWI对蛋白质磷酸化和异生物刺激反应等分子过程、受体复合物和膜筏等细胞组成以及酶结合等分子功能都有影响。KEGG 通路富集分析获得了 193 个通路。与代谢组学分析结果相同,精氨酸脯氨酸代谢和氮代谢参与了同一条通路。结论RWI 具有镇痛作用,其治疗机制主要涉及精氨酸和脯氨酸代谢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Analgesic Mechanism of Radix Wikstroemia indica “Sweat Soaking Method” Processed Product Based on Metabolomics and Network Pharmacology
Background: RWI has an analgesic effect and is related to metabolites such as 4-pyridoxic acid, l-glutamic acid, and agmatine. It is involved in arginine and proline metabolism, arginine biosynthesis, and alanine, aspartate, and glutamate metabolism. In network pharmacology, there were 404 common targets between RWI and pain diseases, and eight core targets were screened, including SRC, STAT3, and HSP90AA1. GO functional enrichment analysis found that RWI had effects on molecular processes such as protein phosphorylation and response to xenobiotic stimulus, cell composition such as receptor complex and membrane raft, and molecular functions such as enzyme binding. KEGG pathway enrichment analysis obtained 193 pathways. Arginine proline metabolism and nitrogen metabolism are involved in the same pathway as metabolomic analysis. Purpose: To explore the analgesic effect and therapeutic mechanism of RWI processed by “Sweat soaking method”. Materials and methods: The torsion experiment was carried out with acetic acid. The metabolomic analysis of serum samples was carried out based on 1H-NMR technology, and the intersection targets of RWI and pain diseases were screened by network pharmacology for gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. Results: RWI has an analgesic effect and is related to metabolites such as 4-pyridoxic acid, l-glutamic acid, and agmatine. It is involved in arginine and proline metabolism, arginine biosynthesis, and alanine, aspartate, and glutamate metabolism. In network pharmacology, there were 404 common targets between RWI and pain diseases, and eight core targets were screened, including SRC, STAT3, and HSP90AA1. GO functional enrichment analysis found that RWI had effects on molecular processes such as protein phosphorylation and response to xenobiotic stimulus, cell composition such as receptor complex and membrane raft, and molecular functions such as enzyme binding. KEGG pathway enrichment analysis obtained 193 pathways. Arginine proline metabolism and nitrogen metabolism are involved in the same pathway as metabolomic analysis. Conclusion: RWI has an analgesic effect, and its therapeutic mechanism mainly involves arginine and proline metabolism.
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