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Gallic Acid Content in Taiwanese Teas at Different Degrees of Fermentation and Its Antioxidant Activity by Inhibiting PKC delta Activation: In Vitro and in Silico Studies

机译:通过抑制PKC DELTA活化的不同发酵度的台湾茶及其抗氧化活性的加仑酸含量:体外和硅研究

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摘要

Teas can be classified according to their degree of fermentation, which has been reported to affect both the bioactive components in the teas and their antioxidative activity. In this study, four kinds of commercial Taiwanese tea at different degrees of fermentation, which include green (non-fermented), oolong (semi-fermented), black (fully fermented), and Pu-erh (post-fermented) tea, were profiled for catechin levels by using high performance liquid chromatography (HPLC). The result indicated that the gallic acid content in tea was directly proportional to the degree of fermentation in which the lowest and highest gallic acid content were 1.67 and 21.98 mg/g from green and Pu-erh tea, respectively. The antioxidative mechanism of the gallic acid was further determined by in vitro and in silico analyses. In vitro assays included the use of phorbol ester-induced macrophage RAW264.7 cell model for determining the inhibition of reactive oxygen species (ROS) production, and PKC delta and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase subunit (p47) activations. The results showed that only at a concentration of 5.00 mu M could gallic acid significantly (p < 0.05) reduce ROS levels in phorbol ester-activated macrophages. Moreover, protein immunoblotting expressed similar results in which activations of PKC delta and p47 were only significantly (p < 0.05) attenuated by 5.00 mu M treatment. Lastly, in silico experiments further revealed that gallic acid could block PKC delta activation by occupying the phorbol ester binding sites of the protein.
机译:茶可以根据其发酵程度进行分类,据报道,据报道,以影响茶和抗氧化活性的生物活性成分。在这项研究中,包括绿色(非发酵),乌龙(半发酵),黑色(全发酵)和Pu-erh(发酵后)茶的四种商业台湾茶通过使用高效液相色谱法(HPLC)对儿茶素水平进行分析。结果表明,茶中的没药物含量与发酵程度成比例,其中最低和最高的无碱酸含量为1.67和21.98mg / g,绿色和普洱茶。通过体外和硅分析进一步测定无氧化酸的抗氧化机制。体外测定包括使用Phorbol酯诱导的巨噬细胞Raw264.7细胞模型来确定反应性氧(ROS)生产的抑制,以及PKC Delta和烟酰胺腺嘌呤二核苷酸磷酸酯(NADPH)氧化酶亚基(P47)活化。结果表明,只有5.00μm的浓度可以显着才能显着(p <0.05)减少博士酯活化巨噬细胞中的ROS水平。此外,蛋白质免疫印迹表达了类似的结果,其中PKC Delta和P47的活性仅显着(P <0.05)减去5.00μm的处理。最后,在硅实验中,进一步揭示了通过占据蛋白质的Phorbol酯结合位点来阻断PKC Delta活化。

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