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肌痛性脑脊髓炎患者和健康志愿者中色氨酸代谢物的非靶向代谢组学与定量分析:一项使用高分辨率质谱的比较研究

Untargeted Metabolomics and Quantitative Analysis of Tryptophan Metabolites in Myalgic Encephalomyelitis Patients and Healthy Volunteers: A Comparative Study Using High-Resolution Mass Spectrometry.

作者信息

Abujrais Sandy, Vallianatou Theodosia, Bergquist Jonas

机构信息

Analytical Chemistry and Neurochemistry, Department of Chemistry─BMC, Uppsala University, Box 599, 751 24 Uppsala, Sweden.

The ME/CFS Collaborative Research Centre at Uppsala University, 751 24 Uppsala, Sweden.

出版信息

ACS Chem Neurosci. 2024 Oct 2;15(19):3525-3534. doi: 10.1021/acschemneuro.4c00444. Epub 2024 Sep 20.

Abstract

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a chronic, complex illness characterized by severe and often disabling physical and mental fatigue. So far, scientists have not been able to fully pinpoint the biological cause of the illness and yet it affects millions of people worldwide. To gain a better understanding of ME/CFS, we compared the metabolic networks in the plasma of 38 ME/CFS patients to those of 24 healthy control participants. This involved an untargeted metabolomics approach in addition to the measurement of targeted substances including tryptophan and its metabolites, as well as tyrosine, phenylalanine, B vitamins, and hypoxanthine using liquid chromatography coupled to mass spectrometry. We observed significant alterations in several metabolic pathways, including the vitamin B3, arginine-proline, and aspartate-asparagine pathways, in the untargeted analysis. The targeted analysis revealed changes in the levels of 3-hydroxyanthranilic acid, 3-hydroxykynurenine, hypoxanthine, and phenylalanine in ME/CFS patients compared to the control group. These findings suggest potential alterations in immune system response and oxidative stress in ME/CFS patients.

摘要

肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)是一种慢性、复杂的疾病,其特征是严重且常常使人衰弱的身心疲劳。到目前为止,科学家们尚未能够完全确定该疾病的生物学病因,但它却影响着全球数百万人。为了更好地了解ME/CFS,我们将38名ME/CFS患者血浆中的代谢网络与24名健康对照参与者的代谢网络进行了比较。这除了使用液相色谱-质谱联用技术测量包括色氨酸及其代谢物、酪氨酸、苯丙氨酸、B族维生素和次黄嘌呤在内的目标物质外,还采用了非靶向代谢组学方法。在非靶向分析中,我们观察到包括维生素B3、精氨酸-脯氨酸和天冬氨酸-天冬酰胺途径在内的几种代谢途径有显著改变。靶向分析显示,与对照组相比,ME/CFS患者中3-羟基邻氨基苯甲酸、3-羟基犬尿氨酸、次黄嘌呤和苯丙氨酸的水平发生了变化。这些发现表明ME/CFS患者的免疫系统反应和氧化应激可能发生了改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddb7/11450765/9d193f373478/cn4c00444_0001.jpg

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