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2型糖尿病患者氧化应激的氨基酸特征:靶向探索性代谢组学研究

Amino Acid Signature of Oxidative Stress in Patients with Type 2 Diabetes: Targeted Exploratory Metabolomic Research.

作者信息

Bala Cornelia G, Rusu Adriana, Ciobanu Dana, Bucsa Camelia, Roman Gabriela

机构信息

Department of Diabetes and Nutrition Diseases, "Iuliu Hatieganu" University of Medicine and Pharmacy, 400006 Cluj-Napoca, Romania.

Drug Information Research Centre, "Iuliu Hatieganu" University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.

出版信息

Antioxidants (Basel). 2021 Apr 15;10(4):610. doi: 10.3390/antiox10040610.

Abstract

Oxidative stress plays a key role in the development of chronic diabetes-related complications. Previous metabolomic studies showed a positive association of diabetes and insulin resistance with branched-chain amino acids (AAs) and aromatic AAs. The purpose of this research is to identify distinct metabolic changes associated with increased oxidative stress, as assessed by nitrotyrosine levels, in type 2 diabetes (T2DM). Serum samples of 80 patients with insulin-treated T2DM are analyzed by AA-targeted metabolomics using ultrahigh-performance liquid chromatography/mass spectrometry. Patients are divided into two groups based on their nitrotyrosine levels: the highest level of oxidative stress (Q4 nitrotyrosine) and lower levels (Q1-Q3 nitrotyrosine). The identification of biomarkers is performed in MetaboAnalyst version 5.0 using a t-test corrected for false discovery rate, unsupervised principal component analysis and supervised partial least-squares discriminant analysis (PLS-DA). Four AAs have significantly different levels between the groups for highest and lower oxidative stress. Cysteine, phenylalanine and tyrosine are substantially increased while citrulline is decreased (-value <0.05 and variable importance in the projection [VIP] >1). Corresponding pathways that might be disrupted in patients with high oxidative stress are phenylalanine, tyrosine and tryptophan biosynthesis, arginine biosynthesis, phenylalanine metabolism, cysteine and methionine metabolism and tyrosine metabolism.

摘要

氧化应激在慢性糖尿病相关并发症的发展中起关键作用。先前的代谢组学研究表明,糖尿病和胰岛素抵抗与支链氨基酸(AAs)及芳香族氨基酸呈正相关。本研究的目的是确定与2型糖尿病(T2DM)中通过硝基酪氨酸水平评估的氧化应激增加相关的独特代谢变化。使用超高效液相色谱/质谱联用的AA靶向代谢组学方法分析了80例接受胰岛素治疗的T2DM患者的血清样本。根据患者的硝基酪氨酸水平将其分为两组:氧化应激水平最高组(Q4硝基酪氨酸)和较低水平组(Q1-Q3硝基酪氨酸)。使用针对错误发现率校正的t检验、无监督主成分分析和有监督偏最小二乘判别分析(PLS-DA)在MetaboAnalyst 5.0版本中进行生物标志物鉴定。在氧化应激水平最高组和较低组之间,有四种氨基酸的水平存在显著差异。半胱氨酸、苯丙氨酸和酪氨酸大幅增加,而瓜氨酸减少(p值<0.05且投影变量重要性[VIP]>1)。在高氧化应激患者中可能被破坏的相应途径有苯丙氨酸、酪氨酸和色氨酸生物合成、精氨酸生物合成、苯丙氨酸代谢、半胱氨酸和甲硫氨酸代谢以及酪氨酸代谢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/8071553/8a64e3ca4a73/antioxidants-10-00610-g001.jpg

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