首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >High-throughput serum metabolomics analysis of gouty arthritis rat treated by total saponins of Rhizoma Dioscoreae Makino by UPLC-Q/TOF-MS
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High-throughput serum metabolomics analysis of gouty arthritis rat treated by total saponins of Rhizoma Dioscoreae Makino by UPLC-Q/TOF-MS

机译:UPLC-Q / TOF-MS对Rhizoma dioscoreae Makino的总皂苷治疗痛风性关节炎大鼠的高通量血清代谢组学分析

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摘要

Rhizoma Dioscoreae Makino (RDM) is effective in treating gouty arthritis (GA) and hyperuricacidemia, especially in promoting uric acid excretion and reducing the inflammatory reaction. Bioactive constituents in RDM are mainly steroidal saponins such as dioscin, trillin, protodioscin and protogracillin. However, the mechanism of its anti-GA action is still unclear, owing to the complex pathological and physiological characteristics of GA, and integration of RDM with multiple components, multiple targets and multiple pathways. Herein, a GA rat model was induced with mono-sodium urate (MSU), and RDM reduced inflammation of rat synovium tissue. Through metabolomics analysis, 35 potential biomarkers with significant changes involved in the pathogenesis of GA induced by MSU were identified, and perturbations were restored after RDM treatment. The most correlated pathways involved in D-galac-tose, D-mannose, D-glucose, myoinositol, Phosphatidylcholine (PC) (16:0/16:0), LysoPC (15:0), phosphatidic acid (PA) [18:1(9Z)/18:1(11Z)] and glutathione induced by MSU were galactose metabolism, inositol phosphate metabolism, glycerophospholipid metabolism and glutathione metabolism, and the derivations of all those biomarkers could be regulated by RDM treatment. RDM has a therapeutic effect on GA by intervening in changes in endogenous metabolisms and the related metabolic pathways.
机译:Rhizoma Dioscoreae Makino(RDM)可有效治疗痛风性关节炎(GA)和高刺激血症,特别是在促进尿酸排泄并降低炎症反应方面。 RDM中的生物活性成分主要是甾体皂苷,如Dioscin,Trillin,Protodioscin和Protogracillin。然而,由于Ga的复杂病理和生理特性,其抗GA动作的机制仍然不清楚,并且RDM与多个组分,多个靶标和多种途径的整合。在此,用单钠尿酸钠(MSU)诱导GA大鼠模型,RDM降低大鼠臂膜组织的炎症。通过代谢组科分析,鉴定了35例潜在的MSU诱导的GA发病机制涉及显着变化的生物标志物,并在RDM处理后恢复扰动。涉及D-加拉克延伸,D-甘露糖,D-葡萄糖,肌肌醇,磷脂酰胆碱(PC)(16:0/16:0),溶胶(15:0),磷脂酸(PA)[18] :1(9Z)/ 18:1(11Z)]和MSU诱导的谷胱甘肽是半乳糖代谢,肌醇磷酸盐代谢,甘油磷脂代谢和谷胱甘肽代谢,并且所有这些生物标志物的衍生物可以通过RDM处理来调节。通过干预内源性代谢和相关代谢途径的变化,RDM对GA具有治疗效果。

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