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利用高分辨质谱分析橄榄果次生物和代谢产物作为橄榄油急性摄入生物标志物—研究个体间差异的一种方法。

High Resolution Mass Spectrometric Analysis of Secoiridoids and Metabolites as Biomarkers of Acute Olive Oil Intake-An Approach to Study Interindividual Variability in Humans.

机构信息

iBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal.

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisboa, Portugal.

出版信息

Mol Nutr Food Res. 2018 Jan;62(2). doi: 10.1002/mnfr.201700065. Epub 2017 Dec 19.

Abstract

SCOPE

Phenolic compounds are minor components of extra virgin olive oil (EVOO). Secoiridoids are the major components contributing to the phenolic content of EVOO. Information is lacking regarding their potential as biomarkers for EVOO intake.

METHODS AND RESULTS

Healthy volunteers (n = 9) ingested 50 mL of EVOO in a single dose containing 322 mg kg total phenolic content (caffeic acid equivalents) and 6 mg 20 g hydroxytyrosol and its derivatives. Plasma is collected before (0 h) and at 0.5, 1, 2, 4, and 6 h after ingestion. Urine samples are collected prior to ingestion (0 h) and at 0-4, 4-8, 8-15, and 15-24 h. Samples are analyzed by UPLC coupled with an Exactive Orbitrap MS. Partial least squares discriminant analysis with orthogonal signal correction is applied to screen for metabolites that allow sample discrimination. Plasma biomarkers and urine biomarkers are selected although individual variability is observed among volunteers. Results are in accordance with in vitro experiments performed (in vitro digestion and hepatic microsomal activity assays).

CONCLUSIONS

Plasma (elenolic acid + H ; p-HPEA-EA + H + glucuronide) and urinary (3,4-DHPEA-EA, 3,4-DHPEA-EA + H +glucuronide, methyl 3,4-DHPEA-EA + H +glucuronide) secoiridoid compounds are selected as biomarkers to monitor EVOO intake showing good predictive ability according to multivariate analysis.

摘要

范围

酚类化合物是特级初榨橄榄油(EVOO)的微量成分。赛尔维奥里多苷是赋予 EVOO 酚类含量的主要成分。关于它们作为 EVOO 摄入的生物标志物的潜力的信息尚不清楚。

方法和结果

健康志愿者(n=9)单次摄入 50 毫升 EVOO,其中含有 322 毫克/千克总酚含量(咖啡酸当量)和 6 毫克 20 克羟基酪醇及其衍生物。在摄入前(0 小时)和摄入后 0.5、1、2、4 和 6 小时采集血浆。在摄入前(0 小时)和摄入后 0-4、4-8、8-15 和 15-24 小时采集尿液样本。通过 UPLC 与 Exactive Orbitrap MS 联用分析样品。应用偏最小二乘判别分析加正交信号校正筛选允许样品区分的代谢物。尽管志愿者个体间存在差异,但仍选择血浆生物标志物和尿液生物标志物。结果与体外实验(体外消化和肝微粒体活性测定)一致。

结论

血浆(阿魏酸+H;p-HPEA-EA+H+葡萄糖醛酸)和尿液(3,4-DHPEA-EA、3,4-DHPEA-EA+H+葡萄糖醛酸、甲基 3,4-DHPEA-EA+H+葡萄糖醛酸)中的赛尔维奥里多苷化合物被选为监测 EVOO 摄入的生物标志物,根据多元分析显示出良好的预测能力。

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