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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Structure Characterization and Action Mechanism of an Antiaging New Compound from Gastrodia elata Blume
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Structure Characterization and Action Mechanism of an Antiaging New Compound from Gastrodia elata Blume

机译:来自胃脂榆树抗衰芽新化合物的结构特征及作用机制

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A new compound, bis(4-hydroxybenzyl)ether mono-β-L-galactopyranoside (1), was isolated from the rhizome of Gastrodia elata Blume. Its structure was elucidated using extensive spectroscopic analysis, including 1D and 2D NMR, HR-ESI-TOF-MS, and chemical derivatization. Compound 1 extended the replicative lifespan of K6001 and the chronological lifespan of YOM36 yeast strains. To understand the mechanism of action, oxidative stress assessment, reactive oxygen species (ROS) and malondialdehyde (MDA) levels, catalase (CAT) and total glutathione peroxidase (GPx) activity assays, and replicative lifespan assay of sod1, sod2, uth1, and skn7 yeast mutant strains were performed. Results indicated the significant increase in the survival rate of yeast under oxidative stress after treatment with 1. ROS and MDA levels were reduced significantly. Meanwhile, the activity of CAT and GPx was significantly increased. The lifespan of sod1, sod2, uth1, and skn7 mutants of K6001 was not affected by 1. Furthermore, we investigated the gene expression related to longevity after administrating 1. The significant increase of Sir2 and reduction of Uth1 gene expression in the 1-treated group were observed. These results indicated that antioxidative stress played an important role in the antiaging effect of 1; Sir2 and Uth1 genes were involved in antiaging effects of 1.
机译:新化合物,双(4-羟基苄基)醚醚单β-L-半乳糖醇素(1)与胃脂菌的根茎分离出来。使用广泛的光谱分析阐明其结构,包括1D和2D NMR,HR-ESI-TOF-MS和化学衍生化。化合物1延伸了K6001的重复寿命和YOM36酵母菌株的年代寿命。要了解作用的机制,氧化应激评估,反应性氧物质(ROS)和丙二醛(MDA)水平,过氧化氢酶(CAT)和总谷胱甘肽过氧化物酶(GPX)活性测定和SOD1,SOD2,Uth1和的重复寿命测定进行SKN7酵母突变体菌株。结果表明,用1.ROS和MDA水平显着降低了氧化胁迫下酵母在氧化胁迫下的成活率显着增加。同时,CAT和GPX的活性显着增加。 K6001的SOD1,SOD2,UTH1和SKN7突变体的寿命不受1.此外,我们研究了在施用后与寿命相关的基因表达。在1-处理的1-处理过的SIR2和Uth1基因表达的显着增加和Uth1基因表达的显着增加观察团。这些结果表明,抗氧化应力在1的抗氧化作用中发挥了重要作用; SiR2和Uth1基因参与1的抗衰次效应。

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