4.7 Article

LC-ESI-LTQ-Orbitrap-MS for Profiling the Distribution of Oleacein and Its Metabolites in Rat Tissues

期刊

ANTIOXIDANTS
卷 10, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/antiox10071083

关键词

biotransformation; extra virgin olive oil; hydroxytyrosol; phenolic compound; secoiridoid

资金

  1. CICYT [AGL2016-75329-R]
  2. CIBEROBN from the Instituto de Salud Carlos III
  3. ISCIII from the Ministerio de Ciencia, Innovacion y Universidades (AEI/FEDER, UE)
  4. Generalitat de Catalunya (GC) [2017SGR 196]
  5. Consejo Nacional de Ciencia y Tecnologia (CONACYT) of Mexico
  6. Ministry of Science Innovation and Universities [RYC-2016-19355]

向作者/读者索取更多资源

Using LC-ESI-LTQ-Orbitrap-MS analysis, this study found that oleacein (OLEA) and its metabolites were distributed in various tissues, with unmetabolized OLEA notably present in the heart, suggesting potential implications for cardiovascular disease prevention. The detection of high levels of hydroxytyrosol (OH-TY) and OLEA + CH3 in the small intestine, liver, and plasma, as well as the identification of nine OLEA metabolites, provides deeper insights into the metabolism and tissue distribution of OLEA, contributing to the understanding of its health effects.
The purpose of this work was to study the distribution of oleacein (OLEA) and its metabolites in rat plasma and different tissues, namely brain, heart, kidney, liver, lung, small intestine, spleen, stomach, skin, and thyroid, following the acute intake of a refined olive oil containing 0.3 mg/mL of OLEA. For this purpose, a distribution kinetics study was carried out. The plasma and tissues were collected at 1, 2, and 4.5 h after the intervention, and analyzed by LC-ESI-LTQ-Orbitrap-MS. Unmetabolized OLEA was detected in the stomach, small intestine, liver, plasma and, most notably, the heart. This finding may be useful for the development of new applications of OLEA for cardiovascular disease prevention. Noteworthy are also the high levels of hydroxytyrosol (OH-TY) and OLEA + CH3 found in the small intestine, liver, and plasma, and the detection of nine OLEA metabolites, five of them arising from conjugation reactions. Liver, heart, spleen, and lungs were the target tissues where the metabolites were most distributed. However, it is important to note that OH-TY, in our experimental conditions, was not detected in any target tissue (heart, spleen, thyroids, lungs, brain, and skin). These results shed further light on the metabolism and tissue distribution of OLEA and contribute to understanding the mechanisms underlying its effect in human health.

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