Major Alterations of Phosphatidylcholine and Lysophosphotidylcholine Lipids in the Substantia Nigra Using an Early Stage Model of Parkinson's Disease

被引:55
|
作者
Farmer, Kyle [1 ]
Smith, Catherine A. [1 ]
Hayley, Shawn [1 ]
Smith, Jeffrey [2 ,3 ]
机构
[1] Carleton Univ, Dept Neurosci, Ottawa, ON K1S 5B6, Canada
[2] Carleton Univ, Dept Chem, Ottawa, ON K1S 5B6, Canada
[3] Carleton Univ, Inst Biochem, Ottawa, ON K1S 5B6, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
lipidomic profile; Parkinson's disease; early stage model; 6-hydroxydopamine; HPLC-ESI-MS; MS; RAT MODEL; INDUCED APOPTOSIS; MOUSE MODEL; TIME-COURSE; LYSOPHOSPHATIDYLCHOLINE; DOPAMINE; ACTIVATION; ALPHA; 6-HYDROXYDOPAMINE; CHEMOATTRACTANT;
D O I
10.3390/ijms160818865
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Parkinson's disease (PD) is a progressive neurodegenerative disease affecting the nigrostriatal pathway, where patients do not manifest motor symptoms until >50% of neurons are lost. Thus, it is of great importance to determine early neuronal changes that may contribute to disease progression. Recent attention has focused on lipids and their role in pro- and anti-apoptotic processes. However, information regarding the lipid alterations in animal models of PD is lacking. In this study, we utilized high performance liquid chromatography electrospray ionization tandem mass spectrometry (HPLC-ESI-MS/MS) and novel HPLC solvent methodology to profile phosphatidylcholines and sphingolipids within the substantia nigra. The ipsilateral substantia nigra pars compacta was collected from rats 21 days after an infusion of 6-hydroxydopamine (6-OHDA), or vehicle into the anterior dorsal striatum. We identified 115 lipid species from their mass/charge ratio using the LMAPS Lipid MS Predict Database. Of these, 19 lipid species (from phosphatidylcholine and lysophosphotidylcholine lipid classes) were significantly altered by 6-OHDA, with most being down-regulated. The two lipid species that were up-regulated were LPC (16:0) and LPC (18:1), which are important for neuroinflammatory signalling. These findings provide a first step in the characterization of lipid changes in early stages of PD-like pathology and could provide novel targets for early interventions in PD.
引用
收藏
页码:18865 / 18877
页数:13
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