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The availability of zinc in endosperm, whole grain and bran-enriched wheat crispbreads fed to rats on a Zn-deficient diet

Published online by Cambridge University Press:  09 March 2007

Göran Hallmans
Affiliation:
Departments of Nutritional Research, University of Umeå, S-901 87 Umeå, Sweden Departments of Pathology, University of Umeå, S-901 87 Umeå, Sweden
Rolf Sjöström
Affiliation:
Departments of Biophysics Laboratory, University of Umeå, S-901 87 Umeå, Sweden
Lars Wetter
Affiliation:
Departments of Pathology, University of Umeå, S-901 87 Umeå, Sweden Departments of Plastic Surgery, University of Umeå, S-901 87 Umeå, Sweden
Kenneth R. Wing
Affiliation:
Departments of Oral Radiology, University of Umeå, S-901 87 Umeå, Sweden
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Abstract

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The hypothesis that factors such as dietary fibre and phytate in wheat bran limit the availability of Zn was tested in growing rats fed on low-Zn diets with different wheat crispbreads as the major source of Zn. Six groups of six weanling male rats each were fed on 5 parts semi-synthetic Zn-deficient diet and 1 part wheat-endosperm crispbread for 1 week. At the beginning of the second week, the crispbread in the diet of five groups was exchanged for crispbread made using one of the following wheat flours: (1) whole grain, (2) bran-enriched whole grain, (3) endosperm with Zn added to the whole-grain level, (4) endosperm with Zn added to the bran-enriched level, (5) whole grain with Zn added to the bran-enriched level. These diets were given ad lib. together with deionized water for 2.5 weeks. The relative absorption of Zn was lowest from the three non-supplemented diets (75–82%). All the added Zn was absorbed. As appetite, body-weight increase, Zn absorption, Zn retention and the Zn concentrations in serum and bone differed only slightly among groups fed on diets with similar Zn concentrations, it is concluded that factors such as dietary fibre or phytate in wheat bran limit the availability of Zn in wheat crispbreads very little when all the Zn is needed for growth and development in rats.

Type
Research Article
Copyright
Copyright © The Nutrition Society 1989

References

REFERENCES

Asp, N.-G., Johansson, C.G., Hallmer, H. & Siljeström, M. (1983). Rapid enzymatic assay of insoluble and soluble dietary fiber. Journal of Agricultural and Food Chemistry 31, 476482.CrossRefGoogle ScholarPubMed
Bagheri, S.M. & Gueguen, L. (1981). Influence of wheat bran diets containing unequal amounts of calcium, magnesium, phosphorus and zinc upon the absorption of these minerals in rats. Nutrition Reports International 24, 4756.Google Scholar
Becker, W.M. & Hoekstra, W.G. (1971). The intestinal absorption of zinc. In Trace Elements and Radionuclides. Intestinal Absorption of Metal Ions, pp. 229–256 [Skornya, S.C. and Waldron-Edward, D., editors]. Oxford: Pergamon Press.Google Scholar
Chesters, J.K. & Quarterman, J. (1970). Effects of zinc deficiency on food intake and feeding patterns of rats. British Journal of Nutrition 24, 10611069.CrossRefGoogle ScholarPubMed
Davies, N.T., Carswell, A.J.P. & Mills, C.F. (1985). The effect of variation in dietary calcium intake on the phytate–zinc interaction in rats. In Trace Elements in Man and Animals—TEMA 5 pp. 456–457 [Mills, C.F., Bremner, I. and Chesters, J.K., editors]. Aberdeen: Commonwealth Agricultural Bureaux.Google Scholar
Davies, N.T., Hristic, V. & Flett, A.A. (1977). Phytate rather than fibre in bran as the major determinant of zinc availability to rats. Nutrition Reports International 15, 207214.Google Scholar
Davies, N.T. & Nightingale, R. (1975). The effects of phytate on the intestinal absorption and secretion of zinc, and whole-body retention of Zn, copper, iron and manganese in rats. British Journal of Nutrition 34, 243258.Google Scholar
Davies, N.T. & Olpin, S.E. (1979). Studies on the phytate: zinc molar contents in diets as a determinant of Zn availability to young rats. British Journal of Nutrition 41, 590603.CrossRefGoogle ScholarPubMed
Ellis, R., Morris, E.R. & Philpot, C. (1977). Quantitative determination of phytate in the presence of high inorganic phosphate. Analytical Biochemistry 2, 536539.CrossRefGoogle Scholar
Evans, G.W., Grace, C.I. & Hahn, C. (1973). Homeostatic regulation of zinc absorption in the rat. Proceedings of the Society for Experimental Biology and Medicine 143, 723725.Google Scholar
Hallmans, G. (1978). Absorption of topically applied zinc and changes in zinc metabolism during wound healing. Acta Dermato-Venereologica 58, Suppl. 80.Google Scholar
Hallmans, G., Nilsson, U., Sjöström, R., Wetter, L. & Wing, K. (1987). The importance of the body's need for zinc in determining Zn availability in food: a principle demonstrated in the rat. British Journal of Nutrition 58, 5964.CrossRefGoogle ScholarPubMed
Hallmans, G. & Wing, K. (1978). Effects of early wound healing and wound treatment with zinc tape on intestinal absorption and distribution of zinc in rats. Acta Chirurgica Scandinavica 144, 431439.Google Scholar
House, W.A., Welch, R.M. & van Campen, D.R. (1982). Effect of phytic acid on the absorption, distribution and exogenous excretion of zinc in rats. Journal of Nutrition 112, 941953.Google Scholar
Morris, R.M. & Ellis, R. (1980). Bioavailability to rats of iron and zinc in wheat bran: response to low-phytate bran and effect of the phytate/zinc molar ratio. Journal of Nutrition 110, 20002010.Google Scholar
Reinhold, J.G., Nasr, K., Lahimgarzadeh, A. & Hedayati, H. (1973). Effects of purified phytate and phytate-rich bread upon metabolism of zinc, calcium, phosphorus and nitrogen in man. Lancet 1, 283288.CrossRefGoogle ScholarPubMed
Sandberg, A.-S., Hasselblad, C., Hasselblad, K. & Hulten, L. (1982). The effect of wheat bran on the absorption of minerals in the small intestine. British Journal of Nutrition 48, 185191.CrossRefGoogle ScholarPubMed
Sandström, B., Arvidsson, B., Cederblad, Å. & Björn-Rasmussen, E. (1980). Zinc absorption from composite meals. I. The significance of wheat extraction rate, zinc, calcium, and protein content in meals based on bread. American Journal of Clinical Nutrition 33, 739745.CrossRefGoogle ScholarPubMed
Snedecor, G. & Cochran, W. (1967). Statistical Methods, 6th ed. Ames, Iowa: Iowa State University Press.Google Scholar
Weigand, E. & Kirchgessner, M. (1976a). Radioisotope dilution technique for determination of zinc absorption in vivo. Nutrition and Metabolism 20, 307313.Google Scholar
Weigand, E. & Kirchgessner, M. (1976b). 65Zn-labelled tissue zinc for determination of endogenous fecal excretion in growing rats. Nutrition and Metabolism 20, 314320.Google Scholar
Weigand, E. & Kirchgessner, M. (1978). Homeostatic adjustments in zinc digestion to widely varying dietary zinc intake. Nutrition and Metabolism 22, 101112.Google Scholar
Williams, R.B. & Mills, C.F. (1970). The experimental production of zinc deficiency in the rat. British Journal of Nutrition 24, 9891003.Google Scholar