Zhao Lin-Ru, He Pan, Li Jie, Zhang Ya-Jun, Jiang Jing-Xing, Wu Ying-Ru, Zhang Yue, Li Jia, Liu Cong, Hao Xu-Liang
Shanxi University of Chinese Medicine Jinzhong 030619, China.
Shanxi University Taiyuan 030006, China.
Zhongguo Zhong Yao Za Zhi. 2022 Apr;47(7):1921-1931. doi: 10.19540/j.cnki.cjcmm.20211230.702.
With the ultra high performance liquid chromatography-quadruple-electrostatic field orbitrap high resolution mass spectrometry(UHPLC-Q Exactive Orbitrap-MS)-based metabonomics technology, this study aims to analyze the effect of Chaiqin Ningshen Granules(CNG) on endogenous metabolites in insomnia rats of liver depression syndrome and explore the sleep-improving mechanism of this prescription. Parachlorophenylalanine(PCPA, ip) and chronic stimulation were combined to induce insomnia of liver depression pattern in rats, and the effect of CNG on the macroscopic signs, hemorheology, and neurotransmitters in the hippocampus of insomnia rats of liver depression syndrome was observed. After the administration, rat hippocampus was collected for liquid chromatography-mass spectrometry(LC-MS) analysis of the metabolomics. Principal component analysis(PCA), partial least squares discriminant analysis(PLS-DA), and orthogonal partial least squares discriminant analysis(OPLS-DA) were employed for analyzing the metabolites in rat hippocampus and screening potential biomarkers. MetPA was used to yield the related metabolic pathways and metabolic networks. The results show that the drugs can significantly improve the mental state, liver depression, and blood stasis of rats, significantly increase the content of 5-hydroxytryptamine(5-HT) and gamma aminobutyric acid(GABA) in hippocampus(except low-dose CNG), and significantly reduce the content of glucose(Glu)(except low-dose CNG). Among them, estazolam and high-dose CNG had better effect than others. Metabolomics analysis yielded 27 potential biomarkers related to insomnia. MetPA analysis showed 4 metabolic pathways of estazolam in intervening insomnia and 3 metabolic pathways of high-dose CNG in intervening insomnia, involving purine metabolism, glycerophospholipid metabolism, histidine metabolism, and caffeine metabolism. CNG can alleviate insomnia by regulating endogenous differential metabolites and further related metabolic pathways. The result lays a basis for further elucidating the mechanism of CNG in improving sleep.
本研究采用基于超高效液相色谱 - 四极杆 - 静电场轨道阱高分辨质谱(UHPLC - Q Exactive Orbitrap - MS)的代谢组学技术,旨在分析柴芩宁神颗粒(CNG)对肝郁证失眠大鼠体内内源性代谢物的影响,探讨该方剂改善睡眠的作用机制。采用对氯苯丙氨酸(PCPA,腹腔注射)联合慢性刺激诱导大鼠肝郁型失眠,观察CNG对肝郁证失眠大鼠宏观体征、血液流变学及海马区神经递质的影响。给药后,采集大鼠海马进行代谢组学的液相色谱 - 质谱(LC - MS)分析。采用主成分分析(PCA)、偏最小二乘法判别分析(PLS - DA)和正交偏最小二乘法判别分析(OPLS - DA)对大鼠海马中的代谢物进行分析并筛选潜在生物标志物。利用MetPA生成相关代谢途径和代谢网络。结果显示,药物可显著改善大鼠精神状态、肝郁及血瘀情况,显著提高海马中5 - 羟色胺(5 - HT)和γ - 氨基丁酸(GABA)含量(低剂量CNG除外),显著降低葡萄糖(Glu)含量(低剂量CNG除外)。其中,艾司唑仑和高剂量CNG效果优于其他药物。代谢组学分析得出27个与失眠相关的潜在生物标志物。MetPA分析显示艾司唑仑干预失眠有4条代谢途径,高剂量CNG干预失眠有3条代谢途径,涉及嘌呤代谢、甘油磷脂代谢、组氨酸代谢和咖啡因代谢。CNG可通过调节内源性差异代谢物及进一步的相关代谢途径缓解失眠。该结果为进一步阐明CNG改善睡眠的机制奠定了基础。