首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >High‐throughput lipidomics analysis to discover lipid biomarkers and profiles as potential targets for evaluating efficacy of Kai‐Xin‐San against APP/PS1 transgenic mice based on UPLC–Q/TOF–MS
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High‐throughput lipidomics analysis to discover lipid biomarkers and profiles as potential targets for evaluating efficacy of Kai‐Xin‐San against APP/PS1 transgenic mice based on UPLC–Q/TOF–MS

机译:高通量脂质谱系分析发现脂质生物标志物和曲线作为评估KAI-XIN-SAN对APP / PS1转基因小鼠的潜在目标的潜在靶标,基于UPLC-Q / TOF-MS评估APP / PS1转基因小鼠的疗效

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摘要

Abstract Lipid metabolism has a significant function in the central nervous system and Alzheimer's disease (AD) is an age‐related senile disease characterized by central nerve degeneration. The pathological development of AD is closely related to lipid metabolism disorders. To reveal the influence of Kai‐Xin‐San (KXS) on lipid metabolism in APP/PSI transgenic mice and potential therapeutic targets for treating AD, brain tissue samples were collected and analyzed by high‐throughput lipidomics based on UPLC–Q/TOF‐MS. The collected raw data were processed by multivariate data analysis to discover the potential biomarkers and lipid metabolic profiles. Compared with the control wild‐type mouse group, nine potential lipid biomarkers were found in the AD model group, of which seven were up‐regulated and two were down‐regulated. Orally administrated KXS can reverse the changes in these potential biomarkers. Compared with the model group, a total of six differential metabolites showed a recovery trend and may be potential targets for KXS to treat AD. This study showed that high‐throughput lipidomics can be used to discover the perturbed pathways and lipid biomarkers as potential targets to reveal the therapeutic effects of KXS.
机译:摘要脂质代谢在中枢神经系统中具有重要功能,阿尔茨海默病(AD)是一种与中枢神经变性的年龄相关的老年疾病。 AD的病理发展与脂质代谢障碍密切相关。为了揭示Kai-Xin-San(KXS)对APP / PSI转基因小鼠的脂质代谢的影响以及治疗AD的潜在治疗靶标,基于UPLC-Q / TOF的高通量脂质学分析并分析脑组织样品。多发性硬化症。通过多变量数据分析处理收集的原始数据,以发现潜在的生物标志物和脂质代谢谱。与对照野生型小鼠组相比,在广告模型组中发现了九个潜在的脂质生物标志物,其中七个被上调,两个被测调节。口服管理的KX可以扭转这些潜在的生物标志物的变化。与模型组相比,共六种差分代谢物显示出恢复趋势,并且可能是治疗广告的KX的潜在目标。该研究表明,高通量的脂质族学可用于发现扰动的途径和脂质生物标志物,作为揭示KXS治疗效果的潜在靶标。

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