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The effects of sugar-beet fibre and wheat bran on iron and zinc absorption in rats

Published online by Cambridge University Press:  09 March 2007

Susan J. Fairweather-Tait
Affiliation:
AFRC Institute of Food Research, Colney Lane, Norwich NR4 7UA
A. J. A. Wright
Affiliation:
AFRC Institute of Food Research, Colney Lane, Norwich NR4 7UA
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Abstract

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The addition of 1 g sugar-beet fibre (Beta Fibre) to 3 g semi-synthetic diet resulted in a 54% increase in iron and a 39% increase in zinc absorption in rats. The same amount of non-starch polysaccharides fed as wheat bran (1.9 g) had no effect on Fe absorption but reduced Zn absorption by 9%. The inhibitory effect of wheat bran is probably due to its high phytate content, but there is, as yet, no explanation for the enhancement of Fe and Zn absorption caused by Beta Fibre. If the effect also occurs in man, it will have important implications for high-fibre diets and mineral nutrition.

Type
Minerals: Absorption and Bioavailability
Copyright
Copyright © The Nutrition Society 1990

References

Bailey, N. T. J. (1964). Statistical Methods in Biology, pp. 4749. London: Hodder and Stoughton.Google Scholar
Bjorn-Rasmussen, E., Hallberg, L. & Walker, R. B. (1973). Food iron absorption in man. II. Isotopic exchange of iron between labeled foods and between a food and an iron salt. American Journal of Clinical Nutrition 26, 13111319.CrossRefGoogle Scholar
Cook, J. D., Noble, N. L., Merck, T. A., Lynch, A. R. & Petersburg, S. J. (1983). Effect of fiber on nonheme iron absorption. Gastroenterology 85, 13541358.CrossRefGoogle ScholarPubMed
Englyst, H., Wiggins, H. S. & Cummings, J. H. (1982). Determination of the non-starch polysaccharides in plant foods by gas-liquid chromatography of constituent sugar as alditol acetates. Analyst 107, 307318.CrossRefGoogle ScholarPubMed
Fairweather-Tait, S. J. & Southon, S. (1989). Studies of iron: zinc interactions in adult rats and the effect of iron fortification of two commercial infant weaning products on iron and zinc status of weanling rats. Journal of Nutrition 119, 599606.CrossRefGoogle ScholarPubMed
Fairweather-Tait, S. J. & Wright, A. J. A. (1984). The influence of previous iron intake on the estimation of bioavailability of Fe from a test meal given to rats. British Journal of Nutrition 51, 185191.CrossRefGoogle ScholarPubMed
Fairweather-Tait, S. J. & Wright, A. J. A. (1985). Iron availability from peas (Pisum satirum) and bread containing added pea testa in rats. British Journal of Nutrition 53, 193197.CrossRefGoogle Scholar
Harland, B. F. & Oberleas, D. (1986). Anion-exchange method for determination of phytate in foods: collaborative study. Journal of the Association of Official Analytical Chemists 69, 667670.Google ScholarPubMed
Morris, E. R. & Ellis, R. (1976). Isolation of monoferric phytate from wheat bran and its biological value as an iron source to the rat. Journal of Nutrition 106, 753760.CrossRefGoogle ScholarPubMed
Sandström, B., Davidsson, L., Kivistö, B., Hasselblad, C. & Cederblad, Å. (1987). The effect of vegetables and beet fibre on the absorption of zinc in humans from composite meals. British Journal of Nutrition 58, 4957.CrossRefGoogle ScholarPubMed