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Integration of 1H NMR and UPLC-Q-TOF/MS for a Comprehensive Urinary Metabonomics Study on a Rat Model of Depression Induced by Chronic Unpredictable Mild Stress

机译:1H NMR和UPLC-Q-TOF / MS的集成用于慢性不可预测的轻度应激引起的抑郁模型的综合泌尿代谢组学研究

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摘要

Depression is a type of complex psychiatric disorder with long-term, recurrent bouts, and its etiology remains largely unknown. Here, an integrated approach utilizing 1H NMR and UPLC-Q-TOF/MS together was firstly used for a comprehensive urinary metabonomics study on chronic unpredictable mild stress (CUMS) treated rats. More than twenty-nine metabolic pathways were disturbed after CUMS treatment and thirty-six potential biomarkers were identified by using two complementary analytical technologies. Among the identified biomarkers, nineteen (>10, 11, >16, 17, 21–25, and >27–36) were firstly reported as potential biomarkers of CUMS-induced depression. Obviously, this paper presented a comprehensive map of the metabolic pathways perturbed by CUMS and expanded on the multitude of potential biomarkers that have been previously reported in the CUMS model. Four metabolic pathways, including valine, leucine and isoleucine biosynthesis; phenylalanine, tyrosine and tryptophan biosynthesis; tryptophan metabolism; synthesis and degradation of ketone bodies had the deepest influence in the pathophysiologic process of depression. Fifteen potential biomarkers (>1–>2, >4–>6, >15, >18, >20–>23, >27, >32, >35–>36) involved in the above four metabolic pathways might become the screening criteria in clinical diagnosis and predict the development of depression. Moreover, the results of Western blot analysis of aromatic L-amino acid decarboxylase (DDC) and indoleamine 2, 3-dioxygenase (IDO) in the hippocampus of CUMS-treated rats indicated that depletion of 5-HT and tryptophan, production of 5-MT and altered expression of DDC and IDO together played a key role in the initiation and progression of depression. In addition, none of the potential biomarkers were detected by NMR and LC-MS simultaneously which indicated the complementary of the two kinds of detection technologies. Therefore, the integration of 1H NMR and UPLC-Q-TOF/MS in metabonomics study provided an approach to identify the comprehensive potential depression-related biomarkers and helpful in further understanding the underlying molecular mechanisms of depression through the disturbance of metabolic pathways.
机译:抑郁症是一种复杂的精神疾病,具有长期反复发作的症状,其病因仍然未知。在这里,首先将结合使用 1 NMR和UPLC-Q-TOF / MS的综合方法用于对慢性不可预测的轻度应激(CUMS)治疗的大鼠进行尿液代谢组学研究。 CUMS治疗后,超过29个代谢途径受到干扰,并使用两种互补的分析技术鉴定了36种潜在的生物标志物。在确定的生物标记物中,首先报告了十九种(> 10、11, > 16、17、21–25,和> 27-36 ) CUMS诱发抑郁症的生物标志物。显然,本文介绍了CUMS干扰的代谢途径的完整图谱,并扩展了先前在CUMS模型中报道的多种潜在生物标记物。四个代谢途径,包括缬氨酸,亮氨酸和异亮氨酸的生物合成;苯丙氨酸,酪氨酸和色氨酸的生物合成;色氨酸代谢酮体的合成和降解在抑郁症的病理生理过程中影响最深。十五种潜在的生物标记(> 1 – > 2 ,> 4 – > 6 ,> 15 ,< strong> 18 ,> 20 – > 23 ,> 27 ,> 32 ,> 35 – > 36 )可能成为临床诊断的筛查标准并预测抑郁症的发生。此外,对经CUMS治疗的大鼠海马中的芳香族L-氨基酸脱羧酶(DDC)和吲哚胺2、3-二加氧酶(IDO)的蛋白质印迹分析结果表明,5-HT和色氨酸耗竭,产生了5- MT和DDC和IDO的表达改变共同在抑郁症的发生和发展中起关键作用。此外,NMR和LC-MS均未同时检测到潜在的生物标志物,这表明两种检测技术的互补。因此, 1 1 H NMR和UPLC-Q-TOF / MS在代谢组学研究中的整合提供了一种识别与抑郁症相关的潜在生物标志物的方法,并有助于通过以下方式进一步了解抑郁症的潜在分子机制代谢途径的紊乱。

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