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基于超高效液相色谱-四极杆飞行时间质谱联用技术的(Craib)B. L. Burtt提取物对阿尔茨海默病影响的代谢组学研究

A UPLC-Q-TOF/MS-Based Metabolomics Study on the Effect of (Craib) B. L. Burtt Extract on Alzheimer's Disease.

作者信息

Wang Yang-Yang, Zhou Ning, Si Yan-Po, Bai Zhi-Yao, Li Meng, Feng Wei-Sheng, Zheng Xiao-Ke

机构信息

Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou 450046, China.

The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou 450046, China.

出版信息

Evid Based Complement Alternat Med. 2021 May 28;2021:8868690. doi: 10.1155/2021/8868690. eCollection 2021.

Abstract

A UPLC-Q-TOF/MS-based metabolomics study was carried out to explore the intervening mechanism of (Craib) B. L. Burtt (CF) extract on Alzheimer's disease (AD). The AD model group consisted of senescence-accelerated mouse prone 8 (SAMP8) mice, and the control group consisted of senescence-accelerated mouse resistant 1 (SAMR1) mice. UPLC-Q-TOF/MS detection, multivariate statistical analysis, and pathway enrichment were jointly performed to research the change in metabolite profiling in the urine of AD mice. The result suggested that the metabolite profiling of SAMP8 mice significantly changed at the sixth month compared with SAMR1 mice of the same age, and the principal component analysis (PCA) score scatter plots of the CF group closely resembled those of the control and positive drug (huperzine A, HA) group. A total of 28 metabolites were considered potential biomarkers associated with the metabolism of beta-alanine, glycine, serine, threonine, cysteine, methionine, arginine, proline, and purines in AD mice. Furthermore, the CF group was clustered with the control and positive group and was clearly separated from the model group in the heat map. In conclusion, significant anti-AD effects were firstly observed in mice after treatment with the CF extract, and the urinary metabolomics approach assisted with dissecting the underlying mechanism.

摘要

开展了一项基于超高效液相色谱-四极杆飞行时间质谱联用(UPLC-Q-TOF/MS)的代谢组学研究,以探索[(Craib)B. L. Burtt(CF)提取物]对阿尔茨海默病(AD)的干预机制。AD模型组由快速老化小鼠易感8型(SAMP8)小鼠组成,对照组由快速老化小鼠抗性1型(SAMR1)小鼠组成。联合进行UPLC-Q-TOF/MS检测、多元统计分析和通路富集,以研究AD小鼠尿液中代谢物谱的变化。结果表明,与同龄的SAMR1小鼠相比,SAMP8小鼠在第6个月时代谢物谱发生了显著变化,CF组的主成分分析(PCA)得分散点图与对照组和阳性药物(石杉碱甲,HA)组的散点图非常相似。共有28种代谢物被认为是与AD小鼠中β-丙氨酸、甘氨酸、丝氨酸、苏氨酸、半胱氨酸、蛋氨酸、精氨酸、脯氨酸和嘌呤代谢相关的潜在生物标志物。此外,在热图中,CF组与对照组和阳性组聚类在一起,并与模型组明显分开。总之,首次观察到CF提取物处理后的小鼠具有显著的抗AD作用,并且尿液代谢组学方法有助于剖析其潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b1b/8177975/19f2bb2bbebd/ECAM2021-8868690.001.jpg

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