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血清脂质组学研究揭示红景天提取物对阿尔茨海默病大鼠的保护作用。

Serum lipidomics study reveals protective effects of Rhodiola crenulata extract on Alzheimer's disease rats.

机构信息

Department of Biomedical Engineering, School of Medical Devices, Shenyang Pharmaceutical University, Shenyang 110016, China.

Hainan Institute for Drug Control, Haikou 570311, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Nov 20;1158:122346. doi: 10.1016/j.jchromb.2020.122346. Epub 2020 Aug 26.

Abstract

Alzheimer's disease (AD) is a chronic and progressive neurodegenerative disorder. Rhodiola crenulata extract (RCE) has shown its protective effects on AD, however, the underlying mechanism is still unclear. In this work, serum lipidomics was conducted to reveal the action mechanism of RCE on AD by HPLC coupled with Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). The animal model of AD was reproduced by intrahippocampal injection of Aβ in rats. The novel object recognition test and passive avoidance test were performed to evaluate the protective effects of RCE on AD rats. The differences of lipid metabolism profiles in rats were evaluated by multivariate statistical analysis. Then, the potential lipid biomarkers were identified and the possible mechanism of RCE on AD was elucidated by metabolic pathways analysis. As a result, twenty-eight lipids with significant differences between the control group and the model group were screened out. With the treatment of RCE, 19 lipids in AD rats showed a trend of callback to the normal levels. The results of pathway analysis indicated that the protective effects of RCE on AD might be closely related to the regulation of linoleic acid metabolism, α-linoleic acid metabolism, sphingolipid metabolism and ether lipid metabolism. In conclusion, this study provides a new perspective on the potential intervention mechanism of RCE for AD treatment.

摘要

阿尔茨海默病(AD)是一种慢性且进行性的神经退行性疾病。红景天提取物(RCE)已显示出对 AD 的保护作用,但作用机制尚不清楚。在这项工作中,通过 HPLC 与傅里叶变换离子回旋共振质谱(FT-ICR MS)联用进行血清脂质组学研究,以揭示 RCE 对 AD 的作用机制。通过向大鼠海马内注射 Aβ 复制 AD 动物模型。通过新物体识别测试和被动回避测试来评估 RCE 对 AD 大鼠的保护作用。通过多变量统计分析评估大鼠脂质代谢谱的差异。然后,通过代谢途径分析鉴定潜在的脂质生物标志物,并阐明 RCE 对 AD 的可能作用机制。结果,筛选出对照组和模型组之间有 28 种脂质存在显著差异。用 RCE 治疗后,AD 大鼠的 19 种脂质有回调到正常水平的趋势。途径分析的结果表明,RCE 对 AD 的保护作用可能与调节亚油酸代谢、α-亚油酸代谢、鞘脂代谢和醚脂代谢密切相关。总之,本研究为 RCE 治疗 AD 的潜在干预机制提供了新的视角。

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