Conversion of major soy isoflavone glucosides and aglycones in in vitro intestinal models. Issue 3 (18th November 2013)
- Record Type:
- Journal Article
- Title:
- Conversion of major soy isoflavone glucosides and aglycones in in vitro intestinal models. Issue 3 (18th November 2013)
- Main Title:
- Conversion of major soy isoflavone glucosides and aglycones in in vitro intestinal models
- Authors:
- Islam, Mohammed A.
Punt, Ans
Spenkelink, Bert
Murk, Albertinka J.
Rolaf van Leeuwen, F. X.
Rietjens, Ivonne M. C. M. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mnfr2105-sec-0010" sec-type="section"> <title>Scope</title> <p>This study compares conversion of three major soy isoflavone glucosides and their aglycones in a series of in vitro intestinal models.</p> </sec> <sec id="mnfr2105-sec-0020" sec-type="section"> <title>Methods and results</title> <p>In an in vitro human digestion model isoflavone glucosides were not deconjugated, whereas studies in a Caco‐2 transwell model confirmed that deconjugation is essential to facilitate transport across the intestinal barrier. Deconjugation was shown upon incubation of the isoflavone glucosides with rat as well as human intestinal S9. In incubations with rat intestinal S9 lactase phlorizin hydrolase, glucocerebrosidase, and cytosolic broad‐specific β‐glucosidase all contribute significantly to deconjugation, whereas in incubations with human intestinal S9 deconjugation appeared to occur mainly through the activity of broad‐specific β‐glucosidase. Species differences in glucuronidation and sulfation were limited and generally within an order of magnitude with 7‐<italic>O</italic>‐glucuronides being the major metabolites for all three isoflavone aglycones and the glucuronidation during first pass metabolism being more efficient in rats than in humans. Comparison of the catalytic efficiencies reveals that deconjugation is less efficient than conjugation confirming that aglycones are unlikely to<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mnfr2105-sec-0010" sec-type="section"> <title>Scope</title> <p>This study compares conversion of three major soy isoflavone glucosides and their aglycones in a series of in vitro intestinal models.</p> </sec> <sec id="mnfr2105-sec-0020" sec-type="section"> <title>Methods and results</title> <p>In an in vitro human digestion model isoflavone glucosides were not deconjugated, whereas studies in a Caco‐2 transwell model confirmed that deconjugation is essential to facilitate transport across the intestinal barrier. Deconjugation was shown upon incubation of the isoflavone glucosides with rat as well as human intestinal S9. In incubations with rat intestinal S9 lactase phlorizin hydrolase, glucocerebrosidase, and cytosolic broad‐specific β‐glucosidase all contribute significantly to deconjugation, whereas in incubations with human intestinal S9 deconjugation appeared to occur mainly through the activity of broad‐specific β‐glucosidase. Species differences in glucuronidation and sulfation were limited and generally within an order of magnitude with 7‐<italic>O</italic>‐glucuronides being the major metabolites for all three isoflavone aglycones and the glucuronidation during first pass metabolism being more efficient in rats than in humans. Comparison of the catalytic efficiencies reveals that deconjugation is less efficient than conjugation confirming that aglycones are unlikely to enter the systemic circulation.</p> </sec> <sec id="mnfr2105-sec-0030" sec-type="section"> <title>Conclusion</title> <p>Altogether, the data point at possible differences in the characteristics for intestinal conversion of the major soy isoflavones between rat and human, especially with respect to their deconjugation.</p> </sec> </abstract> … (more)
- Is Part Of:
- Molecular nutrition & food research. Volume 58:Issue 3(2014:Mar.)
- Journal:
- Molecular nutrition & food research
- Issue:
- Volume 58:Issue 3(2014:Mar.)
- Issue Display:
- Volume 58, Issue 3 (2014)
- Year:
- 2014
- Volume:
- 58
- Issue:
- 3
- Issue Sort Value:
- 2014-0058-0003-0000
- Page Start:
- 503
- Page End:
- 515
- Publication Date:
- 2013-11-18
- Subjects:
- Food -- Biotechnology -- Periodicals
Food -- Microbiology -- Periodicals
Nutrition -- Periodicals
Food -- Toxicology -- Periodicals
Nutrition -- Periodicals
Food Microbiology -- Periodicals
Food Technology -- Periodicals
Molecular Biology -- Periodicals
664.0705 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/mnfr.201300390 ↗
- Languages:
- English
- ISSNs:
- 1613-4125
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817992
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3214.xml