常艳芬, 宫文霞, 郑艳红, 李建伟, 周玉枝, 秦雪梅, 杜冠华. 黄芩醇提物干预D-半乳糖致衰老大鼠的尿液代谢组学研究J. 药学学报, 2016,51(1): 86-92. doi: 10.16438/j.0513-4870.2015-0597
引用本文: 常艳芬, 宫文霞, 郑艳红, 李建伟, 周玉枝, 秦雪梅, 杜冠华. 黄芩醇提物干预D-半乳糖致衰老大鼠的尿液代谢组学研究J. 药学学报, 2016,51(1): 86-92. doi: 10.16438/j.0513-4870.2015-0597
CHANG Yan-fen, GONG Wen-xia, ZHENG Yan-hong, LI Jian-wei, ZHOU Yu-zhi, QIN Xue-mei, DU Guan-hua. Urinary metabolomics study of the effects of Scutellaria baicalensis Georgi ethanol extract on D-galactose-induced ratsJ. Acta Pharmaceutica Sinica, 2016,51(1): 86-92. doi: 10.16438/j.0513-4870.2015-0597
Citation: CHANG Yan-fen, GONG Wen-xia, ZHENG Yan-hong, LI Jian-wei, ZHOU Yu-zhi, QIN Xue-mei, DU Guan-hua. Urinary metabolomics study of the effects of Scutellaria baicalensis Georgi ethanol extract on D-galactose-induced ratsJ. Acta Pharmaceutica Sinica, 2016,51(1): 86-92. doi: 10.16438/j.0513-4870.2015-0597

黄芩醇提物干预D-半乳糖致衰老大鼠的尿液代谢组学研究

Urinary metabolomics study of the effects of Scutellaria baicalensis Georgi ethanol extract on D-galactose-induced rats

  • 摘要: 研究黄芩对D-半乳糖致衰老模型大鼠的影响, 初步探讨黄芩的抗衰老作用机制。将SD大鼠随机分为5组, 即空白组、模型组、黄芩低、中、高剂量 (分别为50、100和200 mg·kg-1) 组, 采用皮下注射D-半乳糖 (100 mg·kg-1) 法, 建立亚急性衰老大鼠模型, 并分别评价衰老大鼠的空间学习记忆能力 (Morris water maze) 和自主活动 (open-field test)。采用代谢组学技术对模型大鼠尿液进行NMR数据采集并结合多元统计分析, 探讨抗衰老机制。结果表明, 黄芩3个剂量均能改善衰老大鼠的行为能力。多元统计分析结果显示, 黄芩低中高剂量组能使衰老大鼠尿液中柠檬酸、丙酮酸、乳酸、泛酸、三甲胺和β-羟基丁酸等6个标志物发生不同程度的回调, 主要涉及能量代谢、糖代谢和肠菌代谢等代谢途径的调节, 表明黄芩发挥抗衰老作用与这些途径相关。

     

    Abstract: The purpose of this study is to evaluate the anti-aging effects and reveal the underlying mechanism of Scutellaria baicalensis Georgi ethanol extract (SBG) in D-galactose-induced rats. Fifty rats were randomly divided into five groups: vehicle control group, D-galactose group, and D-galactose combined with 50, 100, 200 mg·kg-1 SBG. A rat aging model was induced by injecting subcutaneously D-galactose (100 mg·kg-1) for ten weeks. At the tenth week, the locomotor activity (in open-field test) and the learning and memory abilities (in Morris water maze test) were examined respectively. The urine was collected using metabolic cages and analyzed by high-resolution 1H NMR spectroscopy combined with multivariate statistical analyses. The SBG at doses of 50, 100 and 200 mg·kg-1 treatments groups could significantly ameliorate aging process in rats' cognitive performance. The 50, 100, 200 mg·kg-1 SBG regulated citrate, pyruvate, lactate, trimethylamine (TMA), pantothenate, β-hydroxybutyrate in urine favorably toward the control group. These biochemical changes are related to the disturbance in energy metabolism, glycometabolism and microbiome metabolism, which is helpful to further understanding the D-galactose induced aging rats and the therapeutic mechanism of SBG.

     

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