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Antioxidant and antiglycation properties of triterpenoid saponins from Aralia taibaiensis traditionally used for treating diabetes mellitus

机译:传统上用于治疗糖尿病的太白檀木三萜皂苷的抗氧化和抗糖基化特性

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摘要

Our previous study has demonstrated that the antidiabetic activity of the extract of root bark of Aralia taibaiensis (EAT) was correlated with its combined antioxidant and antiglycation properties. To confirm further the constituents responsible, 12 triterpenoid saponins were isolated from EAT and examined for their antioxidant and antiglycation activities. The antioxidant activities of the pure compounds and EAT were evaluated by studying the inhibition of lipid peroxidation in rat liver microsomes induced by ascorbate/Fe2+, cumine hydroperoxide (CHP) or CCl4/reduced form of nicotinamide-adenine dinucleotide phosphate (NADPH). The antioxidant capacities were also evaluated by studying the scavenging of 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical. The antiglycation activities of the pure compounds and EAT were evaluated by hemoglobin-δ-gluconolactone (δ-Glu) assay, bovine serum albumin (BSA)-glucose assay and N-acetyl-glycyllysine methyl ester (GK peptide)-ribose assay. EAT outperformed other compounds in all the assays. The compounds with best antioxidant (TA7, TA24 and TA35) and antiglycation (TA21, TA9 and TA24) activities in different assays were screened out. The results suggest that the antioxidant and antiglycation properties of EAT could be explained, at least in part, by the synergistic effect of pure compounds isolated from it.
机译:我们以前的研究表明,台湾Ar木根皮提取物的抗糖尿病活性与其抗氧化和抗糖化特性有关。为了进一步确定负责的成分,从EAT中分离了12种三萜皂苷,并检查了它们的抗氧化和抗糖化活性。通过研究抗坏血酸/ Fe 2 + ,氢过氧化异丙苯(CHP)或CCl 4 诱导的大鼠肝微粒体脂质过氧化的抑制作用,评估纯化合物和EAT的抗氧化活性。烟酰胺-腺嘌呤二核苷酸磷酸(NADPH)的亚型/还原形式。还通过研究清除2,2-二苯基-1-吡啶并肼基(DPPH)自由基来评估其抗氧化能力。通过血红蛋白-δ-葡萄糖酸内酯(δ-Glu)测定,牛血清白蛋白(BSA)-葡萄糖测定和N-乙酰基-甘氨酸赖氨酸甲酯(GK肽)-核糖测定来评估纯化合物和EAT的抗糖化活性。在所有检测中,EAT的性能均优于其他化合物。筛选出在不同测定中具有最佳抗氧化剂(TA7,TA24和TA35)和抗糖基化(TA21,TA9和TA24)活性的化合物。结果表明,EAT的抗氧化和抗糖基化特性至少可以通过从其中分离出的纯化合物的协同作用来解释。

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  • 来源
    《Redox Report》 |2010年第1期|20-28|共9页
  • 作者单位

    Department of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, P.R. China;

    Department of Toxicology, Faculty of Preventive Medicine, Fourth Military Medical University, Xi'an, P.R. China;

    Department of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, P.R. China;

    Department of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, P.R. China;

    Department of Toxicology, Faculty of Preventive Medicine, Fourth Military Medical University, Xi'an, P.R. China;

    Department of Toxicology, Faculty of Preventive Medicine, Fourth Military Medical University, Xi'an, P.R. China;

    Department of Toxicology, Faculty of Preventive Medicine, Fourth Military Medical University, Xi'an, P.R. China;

    Clinical Laboratory, Xijing Hospital, Fourth Military Medical University, Xi'an, P.R. China;

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