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Quantitative Metabolomics by 1H-NMR and LC-MS/MS Confirms Altered Metabolic Pathways in Diabetes

机译:通过1H-NMR和LC-MS / MS进行的定量代谢组学证实了糖尿病患者代谢途径的改变

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Insulin is as a major postprandial hormone with profound effects on carbohydrate, fat, and protein metabolism. In the absence of exogenous insulin, patients with type 1 diabetes exhibit a variety of metabolic abnormalities including hyperglycemia, glycosurea, accelerated ketogenesis, and muscle wasting due to increased proteolysis. We analyzed plasma from type 1 diabetic (T1D) humans during insulin treatment (I+) and acute insulin deprivation (I-) and non-diabetic participants (ND) by 1H nuclear magnetic resonance spectroscopy and liquid chromatography-tandem mass spectrometry. The aim was to determine if this combination of analytical methods could provide information on metabolic pathways known to be altered by insulin deficiency. Multivariate statistics differentiated proton spectra from I- and I+ based on several derived plasma metabolites that were elevated during insulin deprivation (lactate, acetate, allantoin, ketones). Mass spectrometry revealed significant perturbations in levels of plasma amino acids and amino acid metabolites during insulin deprivation. Further analysis of metabolite levels measured by the two analytical techniques indicates several known metabolic pathways that are perturbed in T1D (I-) (protein synthesis and breakdown, gluconeogenesis, ketogenesis, amino acid oxidation, mitochondrial bioenergetics, and oxidative stress). This work demonstrates the promise of combining multiple analytical methods with advanced statistical methods in quantitative metabolomics research, which we have applied to the clinical situation of acute insulin deprivation in T1D to reflect the numerous metabolic pathways known to be affected by insulin deficiency.
机译:胰岛素是一种重要的餐后激素,对碳水化合物,脂肪和蛋白质代谢具有深远的影响。在没有外源胰岛素的情况下,1型糖尿病患者会表现出多种代谢异常,包括高血糖,糖尿,加速生酮以及由于蛋白水解增加引起的肌肉消耗。我们通过 1 H核磁共振波谱法和液相色谱分析了胰岛素治疗(I +),急性胰岛素剥夺(I-)和非糖尿病参与者(ND)期间1型糖尿病(T1D)人的血浆串联质谱。目的是确定分析方法的这种组合是否可以提供有关已知因胰岛素缺乏而改变的代谢途径的信息。多元统计量基于几种在胰岛素剥夺过程中升高的血浆代谢物(乳酸,乙酸盐,尿囊素,酮),将质子谱与I-和I +区分开。质谱分析显示胰岛素剥夺期间血浆氨基酸和氨基酸代谢物水平显着扰动。通过两种分析技术测得的代谢物水平的进一步分析表明,T1D(I-)受干扰的几种已知代谢途径(蛋白质合成和分解,糖异生,生酮作用,氨基酸氧化,线粒体生物能学和氧化应激)。这项工作证明了在定量代谢组学研究中将多种分析方法与先进的统计方法相结合的希望,我们已将其应用于T1D急性胰岛素缺乏的临床情况,以反映已知受胰岛素缺乏影响的众多代谢途径。

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