Hostname: page-component-7479d7b7d-wxhwt Total loading time: 0 Render date: 2024-07-13T11:21:30.087Z Has data issue: false hasContentIssue false

The influence of previous iron intake on the estimation of bioavailability of Fe from a test meal given to rats

Published online by Cambridge University Press:  09 March 2007

Susan J. Fairweather-Tait
Affiliation:
AFRC Food Research Institute, Colney Lane, Norwich NR4 7UA
A. J. A. Wright
Affiliation:
AFRC Food Research Institute, Colney Lane, Norwich NR4 7UA
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. Iron retention and its subsequent distribution from 3 g 59Fe extrinsically-labelled wholewheat flour in rats given a low (8 μg Fe/g)- or high (566 μg Fe/g)-Fe diet during the previous 3 d was measured (Expt 1). The mean (with se) proportion of Fe retained from wholewheat flour was 0.46 (0.04) in the group given the low-Fe diet and 0.15 (0.01) in the group given the high-Fe diet (P < 0.001). There was no difference in distribution of absorbed 59Fe in the tissues examined.

2. The procedure was repeated in rats given diets containing a range of Fe concentrations, groups 1–6 respectively: 8, 77, 136, 334, 566, 1270 μg Fe/g (Expt 2). The mean (with se) proportions of Fe retained in groups 1–6 respectively were 0.60 (0.02), 0.34 (0.02), 0.30 (0.02), 0.20 (0.20), 0.17 (0.02), 0.09 (0.01). Regression analysis showed that Fe retention was a function of the logarithm of the Fe concentration of the diet consumed before the test meal (R -0.997, P < 0.0001) where Fe retained (μg) = 95–28 log10 Fe concentration of diet.

3. Rats were given a low-, medium- or high-Fe diet (8, 136 or 1270 μg Fe/g respectively) for 1 or 2 d instead of 3 d before measuring Fe retention from 3 g wholewheat flour (Expt 3). The mean (with se) proportions of Fe retained in rats given the low-, medium- or high-Fe diets for I d were 0.45 (0.02), 0.25 (0.02) and 0.13 (0.01) (P < 0.001) and for 2 d 0.47 (0.03), 0.31 (0.03) and 0.18 (0.02) (P < 0.001). There were no significant differences in Fe retention from animals given similar diets for 1 or 2 d before the test meal. As in Expt 2 regression analysis showed a highly-significant relationship between Fe retention and the logarithm of the previous dietary Fe concentration in both sets of groups.

4. It was concluded that the amount of Fe retained by rats from a 3 g meal of wholewheat flour depended on the previous dietary Fe intake. Only one meal in the previous 24 h was required to influence the ‘mucosal setting’ since there was no difference in response between rats preloaded for 1 or 2 d before the test meal.

Type
Papers of direct relevance to Clinical and Human Nutrition
Copyright
Copyright © The Nutrition Society 1984

References

Bothwell, T. H., Pirzio-Biroli, G. & Finch, C. A. (1958). Journal of Laboratory and Clinical Medicine 51, 2436.Google Scholar
Callender, S. T. E. (1970). In Iron Deficiency, p. 75. [Hallberg, L., Harveth, H.–G. and Vannotti, A., editors]. London: Academic Press.Google Scholar
Greenberger, N. J., Balcerzak, S. P. & Ackerman, G. A. (1969). Journal of Laboratory and Clinical Medicine 73, 711721.Google Scholar
Hegenauer, J., Ripley, L. & Saltman, P. (1977). In Proteins of Iron Metabolism, pp. 403410 [Brown, E.B., Aisen, P., Fielding, J. and Crichton, R. R., editors]. London: Grune & Stratton.Google Scholar
Linder, M. C., Dunn, V., Isaacs, E., Jones, D., Lim, S., Van Volkom, M. & Munro, H. N. (1975). American Journal of Physiology 228, 196204.CrossRefGoogle Scholar
Moore, C. V. (1964). Iron Metabolism, p. 241. Berlin: Springer–Verlag.CrossRefGoogle Scholar
Pearson, W. N., Reich, M., Frank, H. & Salamat, L. (1967). Journal of Nutrition 92, 5365.CrossRefGoogle Scholar
Pollack, S., Kaufman, R. M. & Crosby, W. H. (1964). Science 144, 10151016.CrossRefGoogle Scholar
Quastler, H., Bensted, J. P. M., Lamerton, L. F. & Simpson, S. M. (1959). British Journal of Radiology 32, 501509.CrossRefGoogle Scholar
Snedecor, G. W. & Cochrane, W. G. (1973). Statistical Methods, 6th ed., p. 59. Ames, Iowa: Iowa State University Press.Google Scholar
Solomons, N. W., Pineda, O., Viteri, F. & Sandstead, H. H. (1983). Journal of Nutrition 113, 337349.CrossRefGoogle Scholar
University of California (1981). In BMDP Statistical Software [Dixon, W. J., editor]. London: University of California Press.Google Scholar
Wheby, M. S. & Crosby, W. H. (1963). Blood 22, 416428.CrossRefGoogle Scholar