MALDI Mass Spectrometric Imaging of Lipids in Rat Brain Injury Models

被引:107
作者
Hankin, Joseph A. [1 ]
Farias, Santiago E. [1 ]
Barkley, Robert M. [1 ]
Heidenreich, Kim [1 ]
Frey, Lauren C. [3 ]
Hamazaki, Kei [2 ]
Kim, Hee-Yong [2 ]
Murphy, Robert C. [1 ]
机构
[1] Univ Colorado Denver, Dept Pharmacol, Aurora, CO USA
[2] NIAAA, Lab Mol Signaling, NIH, Bethesda, MD USA
[3] Univ Colorado Denver, Dept Neurol, Aurora, CO USA
基金
美国国家卫生研究院;
关键词
MALDI; IMS; Imaging mass spectrometry; Sublimation; Brain; Phosphatidylcholine; Ceramide; Traumatic brain injury; Ischemia reperfusion; Brain injury; Alkali metal adduct images; CA1; Hippocampus damage; GERBIL HIPPOCAMPUS; FOREBRAIN ISCHEMIA; MATRIX; PHOSPHOLIPIDS; TISSUE; DAMAGE; IMS;
D O I
10.1007/s13361-011-0122-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Matrix-assisted laser desorption ionization/ionization imaging mass spectrometry (MALDI IMS) with a time-of-flight analyzer was used to characterize the distribution of lipid molecular species in the brain of rats in two injury models. Ischemia/reperfusion injury of the rat brain after bilateral occlusion of the carotid artery altered appearance of the phospholipids present in the hippocampal region, specifically the CA1 region. These brain regions also had a large increase in the ion abundance at m/z 548.5 and collisional activation supported identification of this ion as arising from ceramide (d18:1/18:0), a lipid known to be associated with cellular apoptosis. Traumatic brain injury model in the rat was examined by MALDI IMS and the area of damage also showed an increase in ceramide (d18:1/18:0) and a remarkable loss of signal for the potassium adduct of the most abundant phosphocholine molecular species 16:0/18:1 (PC) with a corresponding increase in the sodium adduct ion. This change in PC alkali attachment ion was suggested to be a result of edema and influx of extracellular fluid likely through a loss of Na/K-ATPase caused by the injury. These studies reveal the value of MALDI IMS to examine tissues for changes in lipid biochemistry and will provide data needed to eventually understand the biochemical mechanisms relevant to tissue injury.
引用
收藏
页码:1014 / 1021
页数:8
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