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High-throughput liquid chromatography mass-spectrometry-driven lipidomics discover metabolic biomarkers and pathways as promising targets to reveal the therapeutic effects of the Shenqi pill

机译:高通量液相色谱法质谱型脂质族学发现代谢生物标志物和途径作为揭示神奇丸的治疗效果的有前途的靶标

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摘要

Lipidomics, a branch of metabonomics, could provide a powerful technique for discovery of lipid molecules to reveal disease status and drug efficacy. The Shenqi pill (SQP) is a representative prescription for clinical application in the prevention and treatment of kidney-yang deficiency syndrome (KYDS). However, its effect mechanism is still not clear. This article aims to reveal the intervention effect of SQP on KYDS from the perspective of lipid metabolism. In this study, SQP was used to intervene in the rat model of KYDS, on the foundation of successfully replicating the rat model of KYDS induced by corticosterone. The MetaboAnalyst tool was used for analysis of the serum metabolic profile and pattern recognition of KYDS model, based on UPLC-SYNAPT-G2-Si-HDMS. Finally, twenty-two potential lipid biomarkers related to the KYDS model were characterized, and the effects of SQP on regulating potential lipid markers in serum of KYDS model were analyzed. There were 10 biomarkers and seven metabolic pathways closely related to SQP therapy for KYDS were found. The action mechanism and targets of SQP in treating KYDS were explored based on high-throughput lipidomics. This work could provide valuable data and scientific evidence in subsequent studies for the treatment of KYDS.
机译:脂多元族学,一种代谢物理学,可以提供一种发现脂质分子的强大技术,以揭示疾病状态和药物效能。神奇丸(SQP)是肾脏缺乏综合征(KYDS)预防和治疗临床应用的代表性处方。但是,它的效果机制仍然不明确。本文旨在从脂质代谢的角度揭示SQP对KYDS的干预效果。在该研究中,SQP用于干预Kyds的大鼠模型,以成功复制皮质酮诱导的Kyds大鼠模型。基于UPLC-Synapt-G2-Si-HDMS,MetaboAnalyst工具用于分析Kyds模型的血清代谢型材和模式识别。最后,分析了与KYDS模型相关的二十二个潜在的脂质生物标志物,分析了SQP对Kyds模型血清调节潜在脂质标志物的影响。发现了10个生物标志物,发现了与KYDS的SQP疗法密切相关的七种代谢途径。基于高通量脂肪族学,探讨了SQP治疗KYDS的动作机制和目标。这项工作可以在随后的kyds研究中提供有价值的数据和科学证据。

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