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一种非靶向代谢组学方法应用于研究三种不同生物活性植物提取物在人血样中的生物利用度和代谢。

An untargeted metabolomics approach applied to the study of the bioavailability and metabolism of three different bioactive plant extracts in human blood samples.

机构信息

Department of Analytical Chemistry, University of Granada, 18071 Granada, Spain.

Institute of Research, Development and Innovation in Biotechnology of Elche (IDiBE) and Molecular and Cell Biology Institute (IBMC), Miguel Hernández University (UMH), 03202 Elche, Spain.

出版信息

Food Funct. 2024 Sep 16;15(18):9176-9190. doi: 10.1039/d4fo01522c.

Abstract

Advances in the understanding of bioavailability and metabolism of bioactive compounds have been achieved primarily through targeted or semi-targeted metabolomics approaches using the hypothesis of potential metabolized compounds. The recent development of untargeted metabolomics approaches can present great advantages in this field, such as in the discovery of new metabolized compounds or to study the metabolism of compounds from multiple matrices simultaneously. Thus, this study proposes the use of an untargeted metabolomics strategy based on HPLC-ESI-QTOF-MS for the study of bioavailability and metabolism of bioactive compounds from different vegetal sources. Specifically, this study has been applied to plasma samples collected in an acute human intervention study using three matrices (, and ). This approach allowed the selection of those significant variables associated with exogenous metabolites derived from the consumption of bioactive compounds for their subsequent identification. As a result, 14, 25 and 3 potential metabolites associated with supplement intake were significantly detected in the plasma samples from volunteers who ingested the (HS), (SM) and (TC) extracts. Furthermore, values have been computed for each detected compound. The results highlight the potential of untargeted metabolomics for rapid and comprehensive analysis when working with a wide range of exogenous metabolites from different plant sources in biological samples.

摘要

生物活性化合物的生物利用度和代谢的理解的进展主要是通过使用潜在代谢化合物的假设的靶向或半靶向代谢组学方法来实现的。最近开发的非靶向代谢组学方法在该领域具有很大的优势,例如可以发现新的代谢物,或者同时研究来自多种基质的化合物的代谢。因此,本研究提出了一种基于 HPLC-ESI-QTOF-MS 的非靶向代谢组学策略,用于研究来自不同植物源的生物活性化合物的生物利用度和代谢。具体来说,本研究应用于急性人体干预研究中采集的血浆样本,使用了三种基质(、和)。这种方法允许选择与生物活性化合物消耗相关的外源性代谢物的显著变量,以便对其进行后续鉴定。结果,在摄入 HS、SM 和 TC 提取物的志愿者的血浆样本中,检测到与补充剂摄入相关的 14、25 和 3 个潜在代谢物。此外,还计算了每个检测到的化合物的 值。结果突出表明,在生物样本中处理来自不同植物源的广泛外源性代谢物时,非靶向代谢组学具有快速和全面分析的潜力。

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