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Metabolomic Profiling of Human Spermatozoa in Idiopathic Asthenozoospermia Patients Using Gas Chromatography-Mass Spectrometry

机译:气相色谱-质谱法对特发性弱精子症患者精子的代谢组学分析

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摘要

The purpose of this study was to describe the first metabolic profile of human sperm cells through the application of an untargeted platform based on gas chromatography-mass spectrometry (GC-MS). Sperm cell samples from patients diagnosed with idiopathic asthenozoospermia (n = 30) and healthy subjects (n = 30) were analyzed using a nontargeted metabolomics method based on GC-MS spectroscopy. The mass spectrometric data were collected using multivariate and univariate analyses to identify metabolites related to idiopathic asthenozoospermia. By using metabolomic strategies, we identified 33 metabolites, 27 of which were decreased in the idiopathic asthenozoospermia group compared with the normozoospermic group and six were increased in idiopathic asthenozoospermia. With respect to human sperm cells, some of these metabolites are reported here for the first time. Pathways for nucleoside, amino acid and energy metabolism, and the Krebs cycle were disturbed and were associated with idiopathic asthenozoospermia. The metabolic profiling provides an important first step in studying the pathophysiological mechanisms involved in IAS, and the identified metabolites may become potential biomarkers for its diagnosis and treatment.
机译:这项研究的目的是通过应用基于气相色谱-质谱(GC-MS)的非靶向平台来描述人类精子细胞的第一个代谢特征。使用基于GC-MS光谱的非靶向代谢组学方法分析了诊断为特发性弱精子症(n = 30)和健康受试者(n = 30)的精子细胞样品。使用多变量和单变量分析收集质谱数据,以鉴定与特发性弱精子症相关的代谢物。通过使用代谢组学策略,我们确定了33种代谢物,其中特发性弱精子症患者中有27种代谢物减少,而特发性弱精子症患者中有6种增加。关于人类精子细胞,其中一些代谢产物首次在此报道。核苷,氨基酸和能量代谢的途径以及克雷布斯循环受到干扰,并与特发性弱精子症有关。代谢谱分析为研究IAS涉及的病理生理机制提供了重要的第一步,并且鉴定出的代谢物可能成为其诊断和治疗的潜在生物标志物。

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