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Detection of Urine Metabolites in a Rat Model of Chronic Fatigue Syndrome before and after Exercise

机译:运动前后慢性疲劳综合征大鼠模型中尿液代谢物的检测

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摘要

Purpose. The aim of the present study was to elucidate the metabolic mechanisms associated with chronic fatigue syndrome (CFS) via an analysis of urine metabolites prior to and following exercise in a rat model. Methods. A rat model of CFS was established using restraint-stress, forced exercise, and crowded and noisy environments over a period of 4 weeks. Behavioral experiments were conducted in order to evaluate the model. Urine metabolites were analyzed via gas chromatography-mass spectrometry (GC-MS) in combination with multivariate statistical analysis before and after exercise. Results. A total of 20 metabolites were detected in CFS rats before and after exercise. Three metabolic pathways (TCA cycle; alanine, aspartate, and glutamate metabolism; steroid hormone biosynthesis) were significantly impacted before and after exercise, while sphingolipid metabolism alone exhibited significant alterations after exercise only. Conclusion. In addition to metabolic disturbances involving some energy substances, alterations in steroid hormone biosynthesis and sphingolipid metabolism were detected in CFS rats. Sphingosine and 21-hydroxypregnenolone may be key biomarkers of CFS, potentially offering evidence in support of immune dysfunction and hypothalamic-pituitary-adrenal (HPA) axis hypoactivity in patients with CFS.
机译:目的。本研究的目的是通过分析大鼠模型运动前后的尿代谢产物,阐明与慢性疲劳综合症(CFS)相关的代谢机制。方法。在4周的时间内使用束缚压力,强迫运动以及拥挤而嘈杂的环境建立了CFS大鼠模型。进行行为实验以评估模型。运动前后通过气相色谱-质谱联用(GC-MS)分析尿液代谢物,并进行多元统计分析。结果。运动前后,在CFS大鼠中共检测到20种代谢产物。运动前后三个代谢途径(TCA循环;丙氨酸,天冬氨酸和谷氨酸代谢;类固醇激素的生物合成)受到显着影响,而仅鞘脂代谢仅在运动后表现出显着变化。结论。除涉及某些能量物质的代谢紊乱外,在CFS大鼠中还检测到类固醇激素生物合成和鞘脂代谢的改变。鞘氨醇和21-羟基孕烯醇酮可能是CFS的关键生物标志物,可能为支持CFS患者的免疫功能障碍和下丘脑-垂体-肾上腺(HPA)轴功能减退提供证据。

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