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Analysis of Phospholipids in Rat Brain Using Liquid Chromatography–Mass Spectrometry
Author(s) -
Norris Carmen,
Fong Bertram,
MacGibbon Alastair,
McJarrow Paul
Publication year - 2009
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/s11745-009-3357-8
Subject(s) - glycerophospholipid , chromatography , chemistry , ethanolamine , tandem mass spectrometry , mass spectrometry , liquid chromatography–mass spectrometry , sphingomyelin , glycerophospholipids , choline , phosphatidylcholine , biochemistry , phospholipid , membrane
The brain is a lipid‐rich organ containing complex polar lipids including phospholipids (PLs) and sphingolipids. These lipids are involved in the structure and function of cell membranes in the brain. We developed a fast and efficient liquid chromatography–tandem mass spectrometry (LC–MS/MS) method to quantify five different classes of PLs [Choline glycerophospholipid (consists of phosphatidyl choline and plasmenyl choline in these samples), ethanolamine glycerophospholipid (consist of phosphatidyl ethanolamine and plasmenyl ethanolamine in these samples), phosphatidyl serine, phosphatidyl inositol, and sphingomyelin] in the brain tissues of 80‐day‐old Wistar rats. The PLs were extracted from rat brain using chloroform/methanol/water. After separation using a hydrophilic high performance liquid chromatography column, PL‐class‐specific fragmentation (head group identification) with a tandem mass spectrometer in positive ion mode was utilized to measure changes in the relative concentration of the five PL classes. The advantage of this approach was its improved specificity over previously reported LC–MS methods. The method had good repeatability (coefficient of variation 3–9%, excluding phosphatidyl inositol) and recovery (92–103%) and compared well with more laborious traditional methods.