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Metabolomic Study of Collagen-Induced Arthritis in Rats and the Interventional Effects of Huang-Lian-Jie-Du-Tang, a Traditional Chinese Medicine

机译:胶原蛋白诱导的大鼠关节炎的代谢组研究及黄连杰 - 杜堂,中医介入作用

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摘要

Huang-Lian-Jie-Du-Tang (HLJDT) is a traditional Chinese medicine (TCM) with anti-inflammatory activity. The present study used a metabolomic approach based on LC-Q-TOF-MS to profile rheumatoid-arthritis- (RA-) related metabolic changes and to investigate the interventional mechanisms of HLJDT in collagen-induced arthritis rats. Forty male Wistar rats were randomly divided into five groups: (1) a model group, (2) a normal control group, (3) a dexamethasone group, (4) a HLJDT group, and (5) a group that received 13 components of HLJDT. Plasma samples were collected 8, 15, and 22 days after the rats were injected with bovine type II collagen. By combining variable importance in the projection values with partial least squares discriminant analysis, 18 potential biomarkers were identified in the plasma samples. The biomarkers were primarily involved in glycerophospholipid metabolism, fatty acid metabolism, tryptophan metabolism, linoleic acid metabolism, phenylalanine metabolism, purine metabolism, arachidonic acid metabolism, and bile acid biosynthesis. Using the potential biomarkers as a screening index, the results suggest that HLJDT can potentially reverse the process of RA by partially regulating fatty acid oxidation and arachidonic acid metabolism. This study demonstrates that a metabolomic strategy is useful for identifying potential RA biomarkers and investigating the underlying mechanisms of a TCM in RA treatment.
机译:Huang-lian-du-Tang(HLJDT)是一种中药(TCM),具有抗炎活动。本研究采用基于LC-Q-TOF-MS的代谢组方法来概述类风湿性关节炎 - (RA-)相关的代谢变化,并研究HLJDT在胶原蛋白诱导的关节炎大鼠中的介入机制。将40只雄性Wistar大鼠随机分为五组:(1)模型组,(2)正常对照组,(3)一种地塞米松组,(4)HLJDT组,以及收到13个组分的组HLJDT。在用牛II型胶原蛋白注射大鼠后8,15和22天收集血浆样品。通过将具有部分最小二乘判别分析的投影值中的变量重要性组合,在等离子体样品中鉴定了18个潜在的生物标志物。生物标志物主要参与甘油磷脂代谢,脂肪酸代谢,色氨酸代谢,亚油酸代谢,苯丙氨酸代谢,嘌呤代谢,花生酸代谢和胆汁酸生物合成。使用潜在的生物标志物作为筛选指标,结果表明HLJDT通过部分调节脂肪酸氧化和花生酸代谢来妨碍RA的过程。本研究表明,代原味策略可用于鉴定潜在的RA生物标志物并研究TCM在RA治疗中的潜在机制。

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