首页> 外文期刊>Phytomedicine : >Olea europaea leaf (Ph.Eur.) extract as well as several of its isolated phenolics inhibit the gout-related enzyme xanthine oxidase.
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Olea europaea leaf (Ph.Eur.) extract as well as several of its isolated phenolics inhibit the gout-related enzyme xanthine oxidase.

机译:油橄榄叶(Ph.Eur。)提取物及其几种酚类物质可抑制痛风相关酶黄嘌呤氧化酶。

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In Mediterranean folk medicine Olea europaea L. leaf (Ph.Eur.) preparations are used as a common remedy for gout. In this in vitro study kinetic measurements were performed on both an 80% ethanolic (v/v) Olea europaea leaf dry extract (OLE) as well as on nine of its typical phenolic constituents in order to investigate its possible inhibitory effects on xanthine oxidase (XO), an enzyme well known to contribute significantly to this pathological process. Dixon and Lineweaver-Burk plot analysis were used to determine K(i) values and the inhibition mode for the isolated phenolics, which were analysed by RP-HPLC for standardisation of OLE. The standardised OLE as well as some of the tested phenolics significantly inhibited the activity of XO. Among these, the flavone aglycone apigenin exhibited by far the strongest effect on XO with a K(i) value of 0.52 muM. In comparison, the known synthetic XO inhibitor allopurinol, used as a reference standard, showed a K(i) of 7.3 muM. Although the phenolic secoiridoid oleuropein, the main ingredient of the extract (24.8%), had a considerable higher K(i) value of 53.0 muM, it still displayed a significant inhibition of XO. Furthermore, caffeic acid (K(i) of 11.5 muM; 1.89% of the extract), luteolin-7-O-beta-D-glucoside (K(i) of 15.0 muM; 0.86%) and luteolin (K(i) of 2.9 muM; 0.086%) also contributed significantly to the XO inhibiting effect of OLE. For oleuropein, a competitive mode of inhibition was found, while all other active substances displayed a mixed mode of inhibition. Tyrosol, hydroxytyrosol, verbascoside, and apigenin-7-O-beta-D-glucoside, which makes up for 0.3% of the extract, were inactive in all tested concentrations. Regarding the pharmacological in vitro effect of apigenin-7-O-beta-D-glucoside, it has to be considered that it is transformed into the active apigenin aglycone in the mammalian body, thus also contributing substantially to the anti-gout activity of olive leaves. For the first time, this study provides a rational basis for the traditional use of olive leaves against gout in Mediterranean folk medicine.
机译:在地中海民间医学中,油橄榄(Olea europaea L. leaf)(Ph.Eur。)制剂被用作痛风的常用疗法。在这项体外研究中,对80%乙醇(v / v)油橄榄叶干提取物(OLE)及其9种典型酚类成分进行了动力学测量,以研究其对黄嘌呤氧化酶的可能抑制作用( XO),一种众所周知的酶,可大大促进这一病理过程。使用Dixon和Lineweaver-Burk图分析来确定分离的酚类的K(i)值和抑制模式,并通过RP-HPLC对OLE的标准化进行了分析。标准化的OLE以及一些经过测试的酚类均显着抑制XO的活性。其中,黄酮苷元芹菜素对XO的作用最强,K(i)值为0.52μM。相比之下,用作参考标准的已知合成XO抑制剂别嘌呤醇的K(i)为7.3μM。尽管提取物的主要成分酚类类香豆油类橄榄苦苷(占24.8%)具有较高的K(i)值(53.0μM),但仍显示出对XO的显着抑制作用。此外,咖啡酸(K(i)为11.5μM;占提取物的1.89%),木犀草素7-O-β-D-葡萄糖苷(K(i)为15.0μM; 0.86%)和木犀草素(K(i) 2.9μM; 0.086%)也显着促进了OLE的XO抑制作用。对于橄榄苦苷,发现了竞争性抑制模式,而所有其他活性物质均表现出混合抑制模式。占提取物的0.3%的酪醇,羟基酪醇,马齿bas苷和芹菜素7-O-β-D-葡萄糖苷在所有测试浓度下均无活性。关于芹菜素-7-O-β-D-葡萄糖苷的体外药理作用,必须考虑将其转化为哺乳动物体内的活性芹菜素糖苷配基,因此也对橄榄的抗痛风活性有重要贡献。树叶。这项研究首次为地中海民间医学中橄榄叶对痛风的传统使用提供了合理的基础。

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