Hostname: page-component-848d4c4894-mwx4w Total loading time: 0 Render date: 2024-06-26T00:09:01.310Z Has data issue: false hasContentIssue false

The effect of wheat bran on the absorption and accumulation of cadmium in rats

Published online by Cambridge University Press:  09 March 2007

Anncatherine Moberg
Affiliation:
Department of Nutritional Research, University of Umeå, S-901 87 Umeå, Sweden
Göran Hallmans
Affiliation:
Department of Pathology, University of Umeå, S-901 87 Umeå, Sweden
Rolf Sjöström
Affiliation:
Biophysics Laboratory, University of Umeå, S-901 87 Umeå, Sweden
Kenneth R. Wing
Affiliation:
Department of Oral Roentgenology, University of Umeå, S-901 87 Umeå, Sweden
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

1. The major purpose of the present study was to determine whether the addition of wheat bran to endosperm crisp bread in a composite diet given to rats for 6 weeks causes an increase in the accumulation of cadmium in the rats due to the Cd content in the bran, or whether binding factors in the bran, such as dietary fibre and phytic acid, reduce or prevent the accumulation of this Cd. A second purpose was to determine whether the accumulation of Cd can be estimated by measuring the absorption of 199Cd given in a single meal of the diet.

2. Three groups of eight rats were fed on one of three diets. Half of each diet consisted of a basal mixture of starch, protein, oil, minerals and vitamins. The remainder consisted of crisp breads based on refined wheat flour (endosperm group), wheat flour + bran in equal amounts (bran group) and wheat flour + Cd to give a Cd content similar to that of the bran group (endosperm + Cd group). After 41 d on the diets, the rats were deprived of food but not water for 12 h and then given a 5 g test meal of their respective diets with 109Cd added. After 3 h the remaining 109Cd-labelled diets were replaced with the unlabelled diets for 3 h before the rats were killed.

3. The total Cd contents in the wall of the proximal small intestine, including mucus, and in the liver and kidneys were highest in the endosperm + Cd group and lowest in the endosperm group. The amounts of Cd in the intestinal wall, including mucus, and in the liver and kidneys which derived from the test meal (calculated from 109Cd accumulation) were significantly higher in the endosperm + Cd group than in either of the other two groups. The concentration of Cd in the organs of the bran group which derived from the test meal was not significantly greater than that in the endosperm group.

4. The individual variation in Cd content in the liver and kidneys make it very difficult to demonstrate differences in Cd accumulation from the relatively low, naturally occurring Cd concentrations in the diets. Differences in the absorption of 109Cd from test meals indicate that very little of the Cd in bran is available for absorption.

Type
Clinical and Human Nutrition papers: Other Studies Relevant to Human Nutrition
Copyright
Copyright © The Nutrition Society 1987

References

REFERENCES

Andersson, A. (1982). Svensk Veterinärtidning. 34, 481485.Google Scholar
Andersson, A. & Pettersson, O. (1981). Swedish Journal of Agriculture Research 11, 4955.Google Scholar
Asp, N.-G., Johansson, C.-G., Hallmer, H. & Siljeström, M. (1983). Journal of Agricultural and Food Chemistry 31, 476482.CrossRefGoogle Scholar
Björn-Rasmussen, E. (1983). Lancet i, 914916.CrossRefGoogle Scholar
Björn-Rasmussen, E., Hallberg, L. & Walker, R. B. (1972). American Journal of Clinical Nutrition 25, 317323.CrossRefGoogle Scholar
Bjorn-Rasmussen, E., Hallberg, L. & Walker, R. B. (1973). American Journal of Clinical Nutrition 26, 13111319.CrossRefGoogle Scholar
Ellis, R., Morris, E. R. & Philpot, C. (1977). Analytical Biochemistry 77, 536539.CrossRefGoogle Scholar
Engstöm, B. & Norberg, G. F. (1979). Acta Pharmacologica et Toxicologica 45, 315324.CrossRefGoogle Scholar
Evans, G. W. & Johnson, P. E. (1977). American Journal of Clinical Nutrition 30, 873878.CrossRefGoogle Scholar
Friberg, L., Piscator, M., Nordberg, G. F. & Kjellstöm, T. (1974). Cadmium in the Environment, 2nd ed. Cleveland, Ohio: CRC Press.Google Scholar
Jackl, G. A., Rambeck, W. A. & Kollmer, W. E. (1985). Biological Trace Element Research 7, 6974.CrossRefGoogle Scholar
Jorhem, L., Mattsson, P. & Slorach, S. (1984). Vär Föda 36 Suppl.3.Google Scholar
Kiyozumi, M., Miyata, K., Takahashi, Y., Mizunaga, F., Mishima, M., Noda, S., Nakagawa, M. & Kojima, S. (1982). Chemical and Pharmaceutical Bulletin 30, 44944499.CrossRefGoogle Scholar
Omori, M. & Muto, Y. (1977). Journal of Nutritional Science and Vitaminolog 23, 361373.CrossRefGoogle Scholar
Ovesen, L., Bendtsen, F., Tage-Jensen, U., Pedersen, N. T., Gram, B. R. & June, S. J. (1986). Gastroenterology 90, 958962.CrossRefGoogle Scholar
Quarterman, J. (1984). In Trace Elements in Man and Animals – TEMA 5, pp. 400401 [Mills, C. F., Bremner, I. and Chesters, J. K., editors]. Aberdeen: Commonwealth Agricultural Bureaux.Google Scholar
Rose, H. E. & Quarterman, J. (1984). Environmental Research 35, 482489.CrossRefGoogle Scholar
Sandberg, A.-S., Hasselblad, C., Hasselblad, K. & Hultén, L. (1982). British Journal of Nutrition 48, 185191.CrossRefGoogle Scholar
Sandström, B.-M., Arvidsson, B., Cederblad, Ä. & Björn-Rasmussen, E. (1980). American Journal of Clinical Nutrition 33, 739745.CrossRefGoogle Scholar
Simpson, K. M., Morris, E. R. & Cook, J. D. (1981). American Journal of Clinical Nutrition 34, 14691478.CrossRefGoogle Scholar