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Metabolomic Study to Evaluate the Transformations of Extra-Virgin Olive Oil’s Antioxidant Phytochemicals During In Vitro Gastrointestinal Digestion

机译:代谢组学研究评估体外胃肠道消化过程中特级初榨橄榄油的抗氧化植物化学物质的转化

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摘要

In this work, different commercial extra-virgin olive oils (EVOO) were subjected to in vitro gastrointestinal digestion and the changes in bioactive compounds were evaluated by ultra-high-pressure liquid chromatography coupled with quadrupole-time-of-flight mass spectrometry, using untargeted metabolomics. As expected, raw EVOO samples were abundant in total sterols (on average: 3007.4 mg equivalents/kg) and tyrosol equivalents (on average: 334.1 mg equivalents/kg). However, the UHPLC-QTOF screening allowed us to annotate 309 compounds, with a large abundance of sterols (219 compounds), followed by polyphenols (67 compounds) and terpenoids. The in vitro gastrointestinal digestion was found to affect the phytochemical composition of the different EVOO samples. In particular, both unsupervised and supervised statistics depicted the modifications of the bioactive profile following gastric and pancreatic phases. Overall, the compounds which resulted as the most affected by the in vitro digestion were flavonoids (cyanidin and luteolin equivalents), whilst relatively high % bioaccessibility values were recorded for tyrosol equivalents during the pancreatic phase (on average, 66%). In this regard, oleuropein-aglycone (i.e., the major phenolic compound in EVOO) was converted to hydroxytyrosol, moving from an average value of 1.3 (prior to the in vitro digestion) up to 9.7 mg equivalents/kg during the pancreatic step. As proposed in the literature, the increase in hydroxytyrosol might be the result of the combined effect of lipase(s) activity and acidic conditions. Taken together, the present findings corroborate the suitability of untargeted metabolomics coupled to in vitro digestion methods to investigate the bioaccessibility of phenolic compounds. In this regard, a significant impact of in vitro gastrointestinal digestion on polyphenolic profiles has been detected, thus suggesting the need to account for actual bioaccessibility values rather than just considering the amounts in the raw commodity.
机译:在这项工作中,对不同的商业特级初榨橄榄油(EVOO)进行了体外胃肠消化,并通过超高压液相色谱结合四极杆飞行时间质谱对生物活性化合物的变化进行了评估,方法是:非靶向代谢组学。不出所料,原始EVOO样品中的总固醇(平均:3007.4 mg当量/ kg)和酪醇当量(平均:334.1 mg当量/ kg)丰富。但是,UHPLC-QTOF筛选允许我们注释309种化合物,其中包含大量的固醇(219种化合物),然后是多酚(67种化合物)和萜类化合物。发现体外胃肠消化影响不同EVOO样品的植物化学组成。特别地,无监督和有监督的统计都描述了胃和胰腺期后生物活性特征的改变。总体而言,受体外消化影响最大的化合物是类黄酮(花青素和木犀草素当量),而在胰腺期,酪醇当量的相对生物利用度百分比相对较高(平均为66%)。在这方面,将橄榄苦苷糖苷配基(即,EVOO中的主要酚类化合物)转化为羟基酪醇,在胰脏步骤中从平均值1.3(在体外消化之前)上升至9.7mg当量/ kg。如文献中所提出的,羟基酪醇的增加可能是脂肪酶活性和酸性条件共同作用的结果。综上所述,本研究结果证实了结合体外消化方法研究酚类化合物的生物可利用性的非靶向代谢组学的适用性。在这方面,已经检测到体外胃肠道消化对多酚谱的显着影响,因此表明需要考虑实际的生物利用度值,而不仅仅是考虑原料商品中的含量。

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