Bala Cornelia G, Rusu Adriana, Ciobanu Dana, Bucsa Camelia, Roman Gabriela
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.
Antioxidants (Basel). 2021 Apr 15;10(4):610. doi: 10.3390/antiox10040610.
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.
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。