| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1220584 | Journal of Pharmaceutical and Biomedical Analysis | 2016 | 8 Pages |
•Provide new data about the metabolism of NAR while crossing the stomach and colon.•Elucidate which metabolites may be responsible for biological effects attributed to NAR.•Provide a wide metabolic profile of NAR by combining two analytical techniques.•A LC-ESI-LQT-Orbitrab-MS enable us to accurately identify NAR metabolites.•A LC-ESI-MS/MS enabled us to accurately idenfify and quantify NAR metabolites.
Several biological activities (antioxidant, anti-inflammatory, anticarcinogenic) are attributed to naringenin (NAR)—a predominant flavonoid of citrus fruit and tomato—despite its low bioavailability after ingestion. NAR undergoes extensive metabolism when crossing the gastrointestinal tract, resulting in enteric, hepatic and microbial metabolites, some of them with recognized beneficial effects on human health. This study sought to provide new insights into the metabolism of NAR in regions of the gastrointestinal tract where it has been less studied: the stomach and colon. With this purpose, liquid chromatography coupled with an electrospray ionization hybrid linear ion trap quadrupole Orbitrap mass spectrometry technique (LC-ESI-LTQ-Orbitrap-MS) was used for an accurate identification of NAR metabolites, and liquid chromatography/electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) on a triple quadrupole was used for their identification and quantification. The combination of both analytical techniques provided a broader metabolic profile of NAR. As far as we know, this is the first in-depth metabolic profiling study of NAR in the stomach of mice. Three of the metabolites determined using the LC-LTQ-Orbitrap could not be identified by LC-ESI-MS/MS in stomach perfusion samples: apigenin, 3-(4-hydroxyphenyl) propionic acid and phloroglucinol. The number of colonic metabolites determined using the LTQ-Orbitrap-MS was more than twice the number identified by LC-ESI-MS/MS.
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