Absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal CaCo-2/TC7 cell model

Flavonoids are biologically active compounds in food with potential health effects. We have used the CaCo-2 cell monolayer model to study the absorption and metabolism of two flavonols, a class of flavonoids, specifically kaempferol and galangin. Metabolism experiments allowed identification of five...

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Main Authors: Robert Barrington, Gary Williamson, Richard N. Bennett, Barry D. Davis, Jennifer S. Brodbelt, Paul A. Kroon
Format: Article
Language:English
Published: Elsevier 2009-01-01
Series:Journal of Functional Foods
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1756464608000121
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spelling doaj-d8a680315bd9459ba22627e83c96b2b22021-04-29T04:39:32ZengElsevierJournal of Functional Foods1756-46462009-01-01117487Absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal CaCo-2/TC7 cell modelRobert Barrington0Gary Williamson1Richard N. Bennett2Barry D. Davis3Jennifer S. Brodbelt4Paul A. Kroon5Institute of Food Research, Norwich Research Park, Norwich NR4 7UA, UKProctor Food Science Department, University of Leeds, Leeds LS2 9JT, UKInstitute of Food Research, Norwich Research Park, Norwich NR4 7UA, UKDepartment of Chemistry and Biochemistry, The University of Texas at Austin, 1 University Station A5300, Austin, TX 78712, USADepartment of Chemistry and Biochemistry, The University of Texas at Austin, 1 University Station A5300, Austin, TX 78712, USAInstitute of Food Research, Norwich Research Park, Norwich NR4 7UA, UK; Corresponding author: Tel.: +44 (0) 1603 255236; fax: +44 (0) 1603 507723.Flavonoids are biologically active compounds in food with potential health effects. We have used the CaCo-2 cell monolayer model to study the absorption and metabolism of two flavonols, a class of flavonoids, specifically kaempferol and galangin. Metabolism experiments allowed identification of five kaempferol conjugates: 3-, 7- and 4′-glucuronide, a sulphate and a glucurono-sulphate; and four galangin conjugates: 3-, 5- and 7-glucuronides, and a sulphate, using specific enzyme hydrolysis, HPLC–MS, and HPLC with post-column metal complexation/tandem MS. Transport studies showed that the flavonols were conjugated inside the cells then transported across the monolayer or effluxed back to the apical side. Sulphated conjugates were preferentially effluxed back to the apical side, whereas glucuronides were mostly transported to the basolateral side. For kaempferol, a small amount of the unconjugated aglycone permeated in both directions, indicating some passive diffusion. When kaempferol-3-glucuronide and quercetin 7-sulphate were applied to either side of the cells, no permeation in either direction was observed, indicating that conjugates cannot re-cross the cell monolayer. Formation of apical kaempferol-7- and 4′-glucuronides was readily saturated, whereas formation of other conjugates at the apical side and all at the basolateral side increased with increasing concentration of kaempferol, implying different transporters are responsible at the apical and basolateral sides. The results highlight the important but complex metabolic changes occurring in flavonoids during absorption.http://www.sciencedirect.com/science/article/pii/S1756464608000121PolyphenolsFavonolsHuman metabolismQuercetinBioavailabilityGlucuronide
collection DOAJ
language English
format Article
sources DOAJ
author Robert Barrington
Gary Williamson
Richard N. Bennett
Barry D. Davis
Jennifer S. Brodbelt
Paul A. Kroon
spellingShingle Robert Barrington
Gary Williamson
Richard N. Bennett
Barry D. Davis
Jennifer S. Brodbelt
Paul A. Kroon
Absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal CaCo-2/TC7 cell model
Journal of Functional Foods
Polyphenols
Favonols
Human metabolism
Quercetin
Bioavailability
Glucuronide
author_facet Robert Barrington
Gary Williamson
Richard N. Bennett
Barry D. Davis
Jennifer S. Brodbelt
Paul A. Kroon
author_sort Robert Barrington
title Absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal CaCo-2/TC7 cell model
title_short Absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal CaCo-2/TC7 cell model
title_full Absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal CaCo-2/TC7 cell model
title_fullStr Absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal CaCo-2/TC7 cell model
title_full_unstemmed Absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal CaCo-2/TC7 cell model
title_sort absorption, conjugation and efflux of the flavonoids, kaempferol and galangin, using the intestinal caco-2/tc7 cell model
publisher Elsevier
series Journal of Functional Foods
issn 1756-4646
publishDate 2009-01-01
description Flavonoids are biologically active compounds in food with potential health effects. We have used the CaCo-2 cell monolayer model to study the absorption and metabolism of two flavonols, a class of flavonoids, specifically kaempferol and galangin. Metabolism experiments allowed identification of five kaempferol conjugates: 3-, 7- and 4′-glucuronide, a sulphate and a glucurono-sulphate; and four galangin conjugates: 3-, 5- and 7-glucuronides, and a sulphate, using specific enzyme hydrolysis, HPLC–MS, and HPLC with post-column metal complexation/tandem MS. Transport studies showed that the flavonols were conjugated inside the cells then transported across the monolayer or effluxed back to the apical side. Sulphated conjugates were preferentially effluxed back to the apical side, whereas glucuronides were mostly transported to the basolateral side. For kaempferol, a small amount of the unconjugated aglycone permeated in both directions, indicating some passive diffusion. When kaempferol-3-glucuronide and quercetin 7-sulphate were applied to either side of the cells, no permeation in either direction was observed, indicating that conjugates cannot re-cross the cell monolayer. Formation of apical kaempferol-7- and 4′-glucuronides was readily saturated, whereas formation of other conjugates at the apical side and all at the basolateral side increased with increasing concentration of kaempferol, implying different transporters are responsible at the apical and basolateral sides. The results highlight the important but complex metabolic changes occurring in flavonoids during absorption.
topic Polyphenols
Favonols
Human metabolism
Quercetin
Bioavailability
Glucuronide
url http://www.sciencedirect.com/science/article/pii/S1756464608000121
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