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Quantitative analysis of phospholipids containing arachidonate and docosahexaenoate chains in microdissected regions of mouse brain

机译:小鼠大脑显微解剖区域中包含花生四烯酸和二十二碳六烯酸链的磷脂的定量分析

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摘要

Phospholipids containing polyunsaturated fatty acyl chains are prevalent among brain lipids, and regional differences in acyl chain distribution appear to have both functional and pathological significance. A method is described in which the combined application of GC and multiple reaction monitoring (MRM) MS yielded precise relative quantitation and approximate absolute quantitation of lipid species containing a particular fatty acyl chain in milligram-sized tissue samples. The method uses targeted MRM to identify specific molecular species of glycerophosphocholine lipids, glycerophospho-ethanolamine lipids, glycerophosphoinositol lipids, glycerophosphoserine lipids, glycero-phosphoglycerol lipids, and phosphatidic acids that contain esterified arachidonate (AA) and docosahexaenoate (DHA) separated during normal phase LC/MS/MS analysis. Quantitative analysis of the AA and DHA in the LC fractions is carried out using negative ion chemical ionization GC/MS and stable isotope dilution strategies. The method has been applied to assess the glycerophospholipid molecular species containing AA and DHA in microdissected samples of murine cerebral cortex and hippocampus. Results demonstrate the potential of this approach to identify regional differences in phospholipid concentration and reveal differences in specific phospholipid species between cortex and hippocampus. These differences may be related to the differential susceptibility of different brain regions to neurodegenerative disorders.
机译:含有多不饱和脂肪酰基链的磷脂在脑脂质中普遍存在,酰基链分布的区域差异似乎具有功能和病理意义。描述了一种方法,其中GC和多反应监测(MRM)MS的组合应用可对毫克大小的组织样品中包含特定脂肪酰基链的脂质种类进行精确的相对定量和近似绝对定量。该方法使用目标MRM来识别在正常阶段分离的包含酯化花生四烯酸(AA)和二十二碳六烯酸(DHA)分离的甘油磷酸胆碱脂,甘油磷酸肌醇脂,甘油磷酸丝氨酸脂,甘油磷酸甘油脂和磷脂酸的特定分子种类/ MS / MS分析。 LC馏分中AA和DHA的定量分析使用负离子化学电离GC / MS和稳定的同位素稀释策略进行。该方法已用于评估小鼠大脑皮层和海马体显微解剖样品中含有AA和DHA的甘油磷脂分子种类。结果证明了这种方法在识别磷脂浓度的区域差异以及揭示皮质和海马之间特定磷脂种类差异方面的潜力。这些差异可能与不同大脑区域对神经退行性疾病的敏感性不同有关。

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