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Simultaneous lipidomic and transcriptomic profiling in mouse brain punches of acute epileptic seizure model compared to controls

机译:与对照组相比急性癫痫发作模型的小鼠脑冲孔同时进行脂质组学和转录组学分析

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摘要

In this study, we report the development of a dual extraction protocol for RNA and lipids, including phospholipids, endocannabinoids, and arachidonic acid, at high spatial resolution, e.g., brain punches obtained from whole frozen brains corresponding to four brain subregions: dorsal hippocampus, ventral hippocampus, basolateral amygdala, and hypothalamus. This extraction method combined with LC/multiple reaction monitoring for lipid quantifi­cation and quantitative PCR for RNA investigation allows lipidomic and transcriptomic profiling from submilligram amounts of tissue, thus benefiting the time and animal costs for analysis and the data reliability due to prevention of biological variability between animal batches and/or tissue heterogeneity, as compared with profiling in distinct animal batches. Moreover, the method allows a higher extraction efficiency and integrity preservation for RNA, while allowing concurrently quantitative analysis of low and high abundant lipids. The method was applied for brain punches obtained 1 h after kainic acid-induced epileptic seizures in mice (n = 10) compared with controls (n = 10), and enabled the provision of valuable new insights into the subregional lipid and RNA changes with epilepsy, highlighting its potential as a new viable tool in quantitative neurobiology.
机译:在这项研究中,我们报告了在高空间分辨率下针对RNA和脂质(包括磷脂,内源性大麻素和花生四烯酸)的双重提取方案的开发,例如,从对应于四个脑子区域的整个冷冻大脑中获得的脑冲头:背侧海马区,腹侧海马,基底外侧杏仁核和下丘脑。这种提取方法结合LC /多重反应监测进行脂质定量和定量PCR进行RNA研究,可从亚毫克量的组织进行脂质组和转录组谱分析,从而避免了生物之间的生物学差异,从而节省了分析的时间和动物成本以及数据可靠性与不同动物批次中的配置文件相比,动物批次和/或组织异质性。此外,该方法可以提高RNA的提取效率和完整性,同时可以同时定量分析低脂和高脂脂质。该方法适用于海藻酸诱导的小鼠癫痫发作(n = 10)与对照组(n = 10)相比在1小时后获得的脑电击,并为癫痫的次区域脂质和RNA变化提供了有价值的新见解,强调了其作为定量神经生物学新可行工具的潜力。

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