Metabolomic study of lipids in serum for biomarker discovery in Alzheimer's disease using direct infusion mass spectrometry

被引:86
作者
Gonzalez-Dominguez, R. [1 ,2 ,3 ,4 ]
Garcia-Barrera, T. [1 ,2 ,3 ,4 ]
Gomez-Ariza, J. L. [1 ,2 ,3 ,4 ]
机构
[1] Univ Huelva, Fac Expt Sci, Dept Chem, Huelva 21007, Spain
[2] Univ Huelva, Fac Expt Sci, CCMM, Huelva 21007, Spain
[3] Univ Huelva, Huelva 21007, Spain
[4] Univ Huelva, Res Ctr Hlth & Environm CYSMA, Huelva 21007, Spain
关键词
Alzheimer's disease; Direct infusion mass spectrometry; Lipidomics; Biomarkers; FATTY-ACID AMIDES; HUMAN BRAIN; IDENTIFICATION; ELECTROSPRAY; OLEAMIDE; NEURODEGENERATION; PHOSPHOLIPASE-D1; PATHOGENESIS; INVOLVEMENT; METABOLITES;
D O I
10.1016/j.jpba.2014.05.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, we demonstrated the potential of direct infusion mass spectrometry for the lipidomic characterization of Alzheimer's disease. Serum samples were extracted for lipids recovery, and directly analyzed using an electrospray source. Metabolomic fingerprints were subjected to multivariate analysis in order to discriminate between groups of patients and healthy controls, and then some key-compounds were identified as possible markers of Alzheimer's disease. Major differences were found in lipids, although some low molecular weight metabolites also showed significant changes. Thus, important metabolic pathways involved in neurodegeneration could be studied on the basis of these perturbations, such as membrane breakdown (phospholipids and diacylglycerols), oxidative stress (prostaglandins, imidazole and histidine), alterations in neurotransmission systems (oleamide and putrescine) and hyperammonaemia (guanidine and arginine). Moreover, it is noteworthy that some of these potential biomarkers have not been previously described for Alzheimer's disease. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:321 / 326
页数:6
相关论文
共 57 条
[1]   CEREBROSPINAL-FLUID TAURINE IN ALZHEIMERS-DISEASE [J].
ALOM, J ;
MAHY, JN ;
BRANDI, N ;
TOLOSA, E .
ANNALS OF NEUROLOGY, 1991, 30 (05) :735-735
[2]   IDENTIFICATION OF FATTY-ACID AMIDES IN HUMAN-PLASMA [J].
ARAFAT, ES ;
TRIMBLE, JW ;
ANDERSEN, RN ;
DASS, C ;
DESIDERIO, DM .
LIFE SCIENCES, 1989, 45 (18) :1679-1687
[3]   Prostaglandins and other lipid mediators in Alzheimer's disease [J].
Bazan, NG ;
Colangelo, V ;
Lukiw, WJ .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2002, 68-9 :197-210
[4]  
Bet L, 1999, NEUROSCI RES COMMUN, V25, P33, DOI 10.1002/(SICI)1520-6769(199907/08)25:1<33::AID-NRC4>3.3.CO
[5]  
2-C
[6]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[7]   Diacylglycerol, when simplicity becomes complex [J].
Carrasco, Silvia ;
Merida, Isabel .
TRENDS IN BIOCHEMICAL SCIENCES, 2007, 32 (01) :27-36
[8]   Presynaptic serotonergic markers in community-acquired cases of Alzheimer's disease: Correlations with depression and neuroleptic medication [J].
Chen, CPLH ;
Alder, JT ;
Bowen, DM ;
Esiri, MM ;
McDonald, B ;
Hope, T ;
Jobst, KA ;
Francis, PT .
JOURNAL OF NEUROCHEMISTRY, 1996, 66 (04) :1592-1598
[9]   Current trends and future requirements for the mass spectrometric investigation of microbial, mammalian and plant metabolomes [J].
Dunn, Warwick B. .
PHYSICAL BIOLOGY, 2008, 5 (01)
[10]   Metabolomics: Current analytical platforms and methodologies [J].
Dunn, WB ;
Ellis, DI .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2005, 24 (04) :285-294