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Phenolic Extracts from Extra Virgin Olive Oils Inhibit Dipeptidyl Peptidase IV Activity: In Vitro Cellular and In Silico Molecular Modeling Investigations

机译:来自特级初榨橄榄油的酚类提取物抑制二肽基肽酶IV活性:体外细胞和硅的分子建模研究

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摘要

Two extra virgin olive oil (EVOO) phenolic extracts (BUO and OMN) modulate DPP-IV activity. The in vitro DPP-IV activity assay was performed at the concentrations of 1, 10, 100, 500, and 1000 μg/mL, showing a dose-dependent inhibition by 6.8 ± 1.9, 17.4 ± 6.1, 37.9 ± 2.4, 57.8 ± 2.9, and 81 ± 1.4% for BUO and by 5.4 ± 1.7, 8.9 ± 0.4, 28.4 ± 7.2, 52 ± 1.3, and 77.5 ± 3.5% for OMN. Moreover, both BUO and OMN reduced the DPP-IV activity expressed by Caco-2 cells by 2.9 ± 0.7, 44.4 ± 0.7, 61.2 ± 1.8, and 85 ± 4.2% and by 3 ± 1.9, 35 ± 9.4, 60 ± 7.2, and 82 ± 2.8%, respectively, at the same doses. The concentration of the most abundant and representative secoiridoids within both extracts was analyzed by nuclear magnetic resonance (1H-NMR). Oleuropein, oleacein, oleocanthal, hydroxytyrosol, and tyrosol, tested alone, reduced the DPP-IV activity, with IC50 of 472.3 ± 21.7, 187 ± 11.4, 354.5 ± 12.7, 741.6 ± 35.7, and 1112 ± 55.6 µM, respectively. Finally, in silico molecular docking simulations permitted the study of the binding mode of these compounds.
机译:两个特级初榨橄榄油(EVOO)酚类提取物(Buo和Omn)调节DPP-IV活性。体外DPP-IV活性测定法在1,10,100,500和1000μg/ mL的浓度下进行,显示剂量依赖性抑制6.8±1.9,17.4±6.1,37.9±2.4,57.8±2.9 Buo的81±1.4%和5.4±1.7,8.9±0.4,28.4±7.2,52±1.3和77.5±3.5%用于OMN。此外,BUO和OMN都将CACO-2细胞表达的DPP-IV活性降低了2.9±0.7,44.4±0.7,61.2±1.8,以及85±4.2%和3±1.9,35±9.4,60±7.2,分别为同一剂量82±2.8%。通过核磁共振(1H-NMR)分析了两种提取物中最丰富和代表性的SecoIridoid的浓度。橄榄苦苷,oleacein,oleocanthal,羟基酪醇,和酪醇,单独测试,分别减少DPP-IV活性,其IC 50的472.3±21.7 187±11.4,354.5±12.7,741.6±35.7,和1112±55.6微米。最后,在硅的分子对接模拟中允许研究这些化合物的结合模式。

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