Instituto de Investigación e Innovación Biomédica de Cádiz (INiBICA), Hospital Universitario Puerta del Mar, Universidad de Cádiz, Cádiz, Spain.
Division of Food and Nutrition Science, Department of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Methods Mol Biol. 2023;2571:115-122. doi: 10.1007/978-1-0716-2699-3_11.
The circulating metabolome of human peripheral blood provides valuable information to investigate the molecular mechanisms underlying the development of diseases and to discover candidate biomarkers. In particular, erythrocytes have been proposed as potential systemic indicators of the metabolic and redox status of the organism. To accomplish wide-coverage metabolomics analysis, the combination of complementary analytical techniques is necessary to manage the physicochemical complexity of the human metabolome. Herein, we describe an untargeted metabolomics method to capture the plasmatic and erythroid metabolomes based on ultrahigh-performance liquid chromatography coupled to high-resolution mass spectrometry, combining reversed-phase liquid chromatography and hydrophilic interaction liquid chromatography. The method provides comprehensive metabolomics fingerprinting of plasma and erythrocyte samples, thereby enabling the elucidation of the distinctive metabolic disturbances behind childhood obesity and associated comorbidities, such as insulin resistance.
人体外周血的循环代谢组为研究疾病发展的分子机制和发现候选生物标志物提供了有价值的信息。特别是,红细胞被认为是机体代谢和氧化还原状态的潜在系统指标。为了实现广泛的代谢组学分析,有必要结合互补的分析技术来处理人体代谢组的物理化学复杂性。在此,我们描述了一种基于超高效液相色谱与高分辨率质谱联用,结合反相液相色谱和亲水相互作用液相色谱的靶向代谢组学方法,以捕获血浆和红细胞代谢组。该方法提供了血浆和红细胞样本的全面代谢组学指纹图谱,从而能够阐明儿童肥胖症及其相关并发症(如胰岛素抵抗)背后的独特代谢紊乱。