Yu Wei, Yang Wei, Zhao Ming-Yan, Meng Xiang-Lin
Department of Intensive Care Unit, First Affiliated Hospital of Harbin Medical University, Harbin, China.
Front Pharmacol. 2020 Sep 25;11:554783. doi: 10.3389/fphar.2020.554783. eCollection 2020.
Chronic glomerulonephritis (CGN) as the culprit of kidney failure can increase the mortality of critically ill patients and seriously threatens people's health all over the world. This study using metabolomics strategy is to reveal the potential therapeutic mechanism-related targets to evaluate the effects of rhein (RH) on CGN rats. Changes of serum metabolites and pathways were analyzed by non-targeted metabolomic method based on liquid chromatography-mass spectrometry (LC-MS) combined with ingenuity pathway analysis. In addition, the levels of biochemical indicators were also detected. A total of 25 potential biomarkers were identified to express serum metabolic turbulence in CGN animal model, and then 16 biomarkers were regulated by RH trending to the normal states. From metabolite enrichment and pathway analysis, pharmacological activity of RH on CGN were mainly involved in six vital metabolic pathways including phenylalanine, tyrosine and tryptophan biosynthesis, phenylalanine metabolism, arachidonic acid metabolism, tricarboxylic acid cycle (TCA cycle), alanine, aspartate, and glutamate metabolism, arginine and proline metabolism. It suggested CGN treatment with RH, which may be mediated interference with metabolic pathway such as amino acid metabolism, arachidonic acid metabolism, and TCA cycle to regulating inflammation, oxidation response and immune regulation against CGN. It showed that metabolomics method offer deeply insight into the therapeutic mechanisms of natural product.
慢性肾小球肾炎(CGN)作为肾衰竭的罪魁祸首,可增加重症患者的死亡率,并严重威胁着全世界人们的健康。本研究采用代谢组学策略,旨在揭示潜在的治疗机制相关靶点,以评估大黄酸(RH)对CGN大鼠的影响。基于液相色谱-质谱联用(LC-MS)的非靶向代谢组学方法结合 Ingenuity 通路分析,分析血清代谢物和通路的变化。此外,还检测了生化指标水平。共鉴定出25种潜在生物标志物,以表达CGN动物模型中的血清代谢紊乱,随后16种生物标志物受RH调节趋于正常状态。通过代谢物富集和通路分析,RH对CGN的药理活性主要涉及六个重要代谢途径,包括苯丙氨酸、酪氨酸和色氨酸生物合成、苯丙氨酸代谢、花生四烯酸代谢、三羧酸循环(TCA循环)、丙氨酸、天冬氨酸和谷氨酸代谢、精氨酸和脯氨酸代谢。这表明用RH治疗CGN,可能是通过干扰氨基酸代谢、花生四烯酸代谢和TCA循环等代谢途径,来调节针对CGN的炎症、氧化反应和免疫调节。结果表明,代谢组学方法为深入了解天然产物的治疗机制提供了依据。