Metabolomics reveals significant impairments in the immune system of the APP/PS1 transgenic mice of Alzheimer's disease

被引:25
|
作者
Gonzalez-Dominguez, Raul [1 ,2 ,3 ,4 ]
Garcia-Barrera, Tamara [1 ,2 ,3 ,4 ]
Vitorica, Javier [5 ,6 ,7 ]
Luis Gomez-Ariza, Jose [1 ,2 ,3 ,4 ]
机构
[1] Univ Huelva, Fac Expt Sci, Dept Chem, Campus El Carmen, Huelva 21007, Spain
[2] Univ Huelva, Fac Expt Sci, CCMM, Huelva 21007, Spain
[3] Univ Huelva, Campus Excellence Int CeiA3, Huelva 21007, Spain
[4] Univ Huelva, Res Ctr Hlth & Environm CYSMA, Huelva 21007, Spain
[5] Univ Seville, Fac Pharm, Dept Bioquim Bromatol Toxicol & Med Legal, Seville, Spain
[6] Ctr Invest Biomed Red Enfermedades Neurodegenerat, Seville, Spain
[7] Univ Seville, CSIC, Hosp Univ Virgen del Rocio, Inst Biomed Sevilla IBiS, Seville, Spain
关键词
Alzheimer's disease; APP/PS1; Metabolomics; Spleen; Thymus; MASS-SPECTROMETRY; OXIDATIVE STRESS; HUMAN BRAIN; GLUTATHIONE; PERFORMANCE; MODEL; MOUSE; CARNITINE; BIOMARKER; RESPONSES;
D O I
10.1002/elps.201400450
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Inflammatory processes and other failures related to the immune system are common features associated with Alzheimer's disease (AD), in both brain and the peripheral system. Thus, the study of the main organs of the immune system may have a great potential for the elucidation of pathological mechanisms underlying these abnormalities. This is the first metabolomic investigation performed in spleen and thymus from transgenic mice of AD. Tissues were fingerprinted using a metabolomic platform comprising GC-MS and ultra-HPLC-MS. Multivariate statistics demonstrated significant differences in numerous metabolites between the APP/PS1 mice and wild-type controls, and it was proven that multiple biochemical pathways are disturbed in these organs including abnormal metabolism of phospholipids, energy deficiencies, altered homeostasis of amino acids, oxidative stress, and others. Therefore, these findings highlight the importance of the proper metabolic functioning of peripheral immune system in the development of neurodegenerative disorders such as AD.
引用
收藏
页码:577 / 587
页数:11
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