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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >NMR-Based Metabonomic Study Reveals Intervention Effects of Polydatin on Potassium Oxonate-Induced Hyperuricemia in Rats
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NMR-Based Metabonomic Study Reveals Intervention Effects of Polydatin on Potassium Oxonate-Induced Hyperuricemia in Rats

机译:基于NMR的代谢性研究揭示了多达丁对大鼠红豆酸诱导的高尿酸血症的干预作用

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Previous studies have disclosed the antihyperuricemic effect of polydatin, a natural precursor of resveratrol; however, the mechanisms of action still remain elusive. The present study was undertaken to evaluate the therapeutic effects and the underlying mechanisms of polydatin on potassium oxonate-induced hyperuricemia in rats through metabonomic technology from a holistic view. Nuclear magnetic resonance (NMR) spectroscopy was applied to capture the metabolic changes in sera and urine collected from rats induced by hyperuricemia and polydatin treatment. With multivariate data analysis, significant metabolic perturbations were observed in hyperuricemic rats compared with the healthy controls. A total of eleven and six metabolites were identified as differential metabolites related to hyperuricemia in serum and urine of rats, respectively. The proposed pathways primarily included branched-chain amino acid (BCAA) metabolism, glycolysis, the tricarboxylic acid cycle, synthesis and degradation of ketone bodies, purine metabolism, and intestinal microflora metabolism. Additionally, some metabolites indicated the risk of renal injury induced by hyperuricemia. Polydatin significantly lowered the levels of serum uric acid, creatinine, and blood urea nitrogen and alleviated the abnormal metabolic status in hyperuricemic rats by partially restoring the balance of the perturbed metabolic pathways. Our findings shed light on the understanding of the pathophysiological process of hyperuricemia and provided a reference for revealing the metabolic mechanism produced by polydatin in the treatment of hyperuricemia.
机译:以前的研究已经公开了多达丁的抗静电血糖作用,白藜芦醇的天然前体;然而,行动机制仍然难以捉摸。本研究进行了通过从整体视野中的代谢族技术来评估多达汀对大鼠钾诱导的大鼠钾诱导的高尿尿症的治疗效果和潜在机制。施用核磁共振(NMR)光谱法捕获由高尿酸血症和多达汀治疗诱导的大鼠收集的血清和尿液中的代谢变化。随着多元数据分析,与健康对照相比,在高尿动大鼠中观察到显着的代谢扰动。将11种和六种代谢物鉴定为与大鼠血清和尿液中的高尿酸血症相关的差异代谢物。所提出的途径主要包括支链氨基酸(BCAA)代谢,糖酵解,三羧酸循环,酮体的合成和降解,嘌呤代谢和肠道微生物代谢。此外,一些代谢产物表明高尿酸血症诱导的肾损伤风险。多达汀显着降低了血清尿酸,肌酐和血尿尿素氮的水平,通过部分恢复扰动代谢途径的平衡来缓解高尿动大鼠的异常代谢状态。我们的研究结果阐明了对高尿酸血症病理生理过程的理解,并为揭示了多达丁治疗高尿酸血症的代谢机制提供了参考。

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