## Abstract Up to now, the metabolism of hispidulin (5,7,4′‐trihydroxy‐6‐methoxyflavone), a potent ligand of the central human benzodiazepine receptor, has not been investigated. To elucidate the metabolism of hispidulin in the large intestine, its biotransformation by the pig caecal microflora was
The pig caecum model: A suitable tool to study the intestinal metabolism of flavonoids
✍ Scribed by Samira Labib; Annette Erb; Michael Kraus; Thomas Wickert; Elke Richling
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 850 KB
- Volume
- 48
- Category
- Article
- ISSN
- 1613-4125
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✦ Synopsis
Abstract
Pig caecum was used under anaerobic conditions to metabolize flavonoids from several classes, i. e., chrysin 1, naringenin 2, quercetin 3, and hesperetin 4. Whereas chrysin 1 was not converted by the pig intestinal flora under the experimental conditions used, naringenin 2 was transformed to 3‐(4‐hydroxyphenyl)‐propionic acid and 3‐phenylpropionic acid. Quercetin 3 was metabolized to phloroglucinol, 3,4‐dihydroxyphenylacetic acid, and 3,4‐dihydroxytoluene. Hesperetin 4 was degraded via eriodictyol to 3‐(3‐hydroxyphenyl)‐propionic acid and phloroglucinol. Structural elucidation of the formed metabolites was performed by high‐performance liquid chromatography – diode array detection (HPLC–DAD) as well as HPLC‐electrospray ionization – mass spectrometry (ESI‐MS (MS)) and high resolution gas chromatography‐mass spectrometry (HRGC‐MS) analyses. The time course of microbial conversion of 2–4 was determined by HPLC‐DAD analysis, revealing slow degradation of 2 and rapid transformation of 3 and 4. The results lead to the conclusion that the pig caecum model is a suitable ex vivo model for studying the intestinal degradation of flavonoids.
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