质谱成像揭示小鼠脑内特定区域脂质变化对依非韦伦治疗的反应

Nav Raj Phulara, Apurv Rege, Charles J. Bieberich, Herana Kamal Seneviratne
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摘要

依非韦伦(EFV)是治疗人类免疫缺陷病毒感染的常用药物,已知会对大脑产生不良影响。虽然已知 EFV 与血浆脂质水平异常有关,但 EFV 治疗后脑组织中单个脂质分子的空间定位变化仍有待探索。在这项研究中,我们采用了基质辅助激光解吸电离质谱成像方法来确定小鼠大脑在接受 EFV 治疗后特定区域的脂质变化。我们检测了小鼠大脑中磷脂酰胆碱(PC)、鞘磷脂(SM)、神经酰胺磷脂酰肌醇(PI-Cer)和己基甘油酰胺(HexCer)分子的独特空间定位模式。有趣的是,PC(32:0)、PC(38:5)和SM(36:1;O2)在EFV处理的小鼠大脑海马区显示出较高的丰度,而PI-Cer(38:8)在EFV处理的小鼠大脑海马区显示出较低的丰度。此外,我们还观察到 PC(38:6)、PC(40:6)和 PI-Cer(40:3)在经 EFV 处理的小鼠大脑丘脑区含量较低。此外,与对照组相比,SM(40:1;O2)、SM(42:2;O2)、SM(42:1;O2)、SM(43:2;O2)和SM(43:1;O2)在EFV处理小鼠大脑的胼胝体区域均有积累。然而,HexCer(42:1;O3)在EFV处理后的胼胝体区域出现了耗竭。为了描述包括脂质代谢酶在内的蛋白质的表达模式对 EFV 处理的反应,我们采用了基于质谱的蛋白质组学方法。结果发现,12 种脑部蛋白质的表达水平在 EFV 治疗后显著下降。综合来看,这些多组学数据为了解 EFV 对脑脂质代谢的影响提供了重要的启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mass Spectrometry Imaging Reveals Region-Specific Lipid Alterations in the Mouse Brain in Response to Efavirenz Treatment

Mass Spectrometry Imaging Reveals Region-Specific Lipid Alterations in the Mouse Brain in Response to Efavirenz Treatment
Efavirenz (EFV) is a commonly used drug to treat human immunodeficiency virus infection and is known to exert adverse effects on the brain. Although it is known that EFV is associated with abnormal plasma lipid levels, the changes in the spatial localization of individual lipid molecules in brain tissue following EFV treatment are yet to be explored. In this study, we employed a matrix-assisted laser desorption/ionization mass spectrometry imaging approach to determine region-specific lipid alterations in mouse brains following EFV treatment. We detected unique spatial localization patterns of phosphatidylcholine (PC), sphingomyelin (SM), ceramide phosphoinositol (PI-Cer), and hexosylceramide (HexCer) molecules in the mouse brain. Interestingly, PC(32:0), PC(38:5), and SM(36:1;O2) showed high abundance in the hippocampus region, whereas PI-Cer(38:8) exhibited low abundance in the hippocampus region of the EFV-treated mouse brains. Additionally, we observed low abundance of PC(38:6), PC(40:6), and PI-Cer(40:3) in the thalamus region of the EFV-treated mouse brains. Furthermore, SM(40:1;O2), SM(42:2;O2), SM(42:1;O2), SM(43:2;O2), and SM(43:1;O2) exhibited their accumulation in the corpus callosum region of the EFV-treated mouse brains as compared to controls. However, HexCer(42:1;O3) exhibited depletion in the corpus callosum region in response to EFV treatment. To characterize the expression patterns of proteins, including lipid metabolizing enzymes, in response to EFV treatment, mass spectrometry-based proteomics was utilized. From these, the expression levels of 12 brain proteins were found to be significantly decreased following EFV treatment. Taken together, these multiomics data provide important insights into the effects of EFV on brain lipid metabolism.
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