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Dietary fibre reduced phenolic acid production from rutin in an ex vivo fermentation model

Published online by Cambridge University Press:  15 April 2015

B. Mansoorian
Affiliation:
Human Nutrition, School of Medicine, College of Medical, Veterinary & Life Sciences University of Glasgow, New Lister Building, Glasgow Royal Infirmary, 10–16 Alexandra Parade, Glasgow City, G31 2ER, Scotland, United Kingdom
A. L. Garcia
Affiliation:
Human Nutrition, School of Medicine, College of Medical, Veterinary & Life Sciences University of Glasgow, New Lister Building, Glasgow Royal Infirmary, 10–16 Alexandra Parade, Glasgow City, G31 2ER, Scotland, United Kingdom
E. Combet
Affiliation:
Human Nutrition, School of Medicine, College of Medical, Veterinary & Life Sciences University of Glasgow, New Lister Building, Glasgow Royal Infirmary, 10–16 Alexandra Parade, Glasgow City, G31 2ER, Scotland, United Kingdom
C. A. Edwards
Affiliation:
Human Nutrition, School of Medicine, College of Medical, Veterinary & Life Sciences University of Glasgow, New Lister Building, Glasgow Royal Infirmary, 10–16 Alexandra Parade, Glasgow City, G31 2ER, Scotland, United Kingdom
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2015 

The health effects of foods rich in polyphenols and fibre are well established but the mechanisms of action are not fully understood. Fibre and polyphenols are usually eaten as part of a meal or even in the same food, but their bioavailability and metabolism have up until now been studied separately. It is therefore important to understand their interactions when combined. Most polyphenols have low bioavailability in the upper gut and fibres are undigested in the small intestine. Both food components reach the colon, where they are metabolised by the colonic bacteria into bioactive compounds e.g. phenolic acids (PA) and short chain fatty acids (SCFA). Raftiline, pectin and ispaghula are dietary fibres with different physicochemical properties, which may modulate colonic bacteria in different ways. Rutin, a polyphenol ubiquitous in plant foods, escapes absorption in the small intestine due to its rhamlose-containing glycosidic moiety. We aimed to study the effect of the interaction between the fibres raftiline, pectin and ispaghula and the polyphenol rutin on PA and SCFA production.

In an ex-vivo fermentation model, 24 h batch cultures of human faecal samples from volunteers (n = 10, 19–33y old) following a 3-day low polyphenol diet were investigated. The cultures were incubated with different combinations of fibres (raftiline, pectin and ispaghula; 1 g/50mL) and rutin (28 μmol/L)(Reference Jaganath, Mullen and Edwards1). Samples were obtained at 0, 2, 4, 6 and 24 h and stored at −80 °C. PA analysis was carried out using GC-MS(Reference Combet, Lean and Boyle2) and SCFA by GC-FID(Reference Edwards, Gibson and Champ3).

The faecal fermentation of rutin resulted in the production of phenylacetic acid (PAA), 4-hydroxybenzoic acid (4-OHBA), 3-hydroxyphenylacetic acid (3-OHPAA), 4-hydroxyphenylacetic acid (4-OHPAA), 3,4-dihydroxyphenylacetic acid (3,4-diOHPAA), 3-hydroxyphenylpropionic acid (3-OHPPA) and 4-hydroxyphenylpropionic acid (4-OHPPA). At 24 h, fermentation with raftiline and pectin inhibited the total phenolic acid formation p = 0·0001 to the same extent (85·5% and 78·3% respectively while fermentation with ispaghula led to a lesser inhibition of PA formation (33·7%, p = 0·03). After 24 h, all fibres significantly reduced PAA and 3,4-diOHPAA formation (Table) as well as the inhibition of 3-OHPAA and 4-OHPAA by pectin and raftiline. There was no impact of rutin on SCFA production.

Values are expressed as mean (SD) for duplicates (n = 10). * Values are significantly different at p < 0·05 (paired t-test for each fibre against rutin).

Dietary fibres inhibit the release of PA from rutin, which is related to the fermentation related mechanisms. This needs to be taken into account when considering the potential health benefits of foods rich in polyphenolics and fibre.

References

1.Jaganath, IB, Mullen, W, Edwards, CA et al. (2006). Free Radic Res 40, 1035–46.Google Scholar
2.Combet, E, Lean, M, Boyle, JG et al. (2011). Clin Chim Acta 412, 165169.Google Scholar
3.Edwards, CA, Gibson, G, Champ, M, et al. (1996). J. Sci. Food Agric. 71, 209217.Google Scholar