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The effect of alcoholic beverages on iron and zinc metabolism in the rat

Published online by Cambridge University Press:  09 March 2007

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

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1. Male Wistar rats (approximately 200 g) were given distilled water and a semi-synthetic control diet for 6 d. On day 7, 37 kBq 65Zn were administered intramuscularly and the rats were given distilled water, beer, cider, red wine, whisky or ethanol as their only source of fluid. The wine, whisky and ethanol were diluted so that each of the beverages contained a similar ethanol concentration (approximately 30 g/1). Food and fluid intake, growth rate and whole-body 65Zn were measured regularly over 11 d, after which animals were killed and blood haemoglobin (Hb) concentration, liver iron stores and the Zn concentration in testes determined.

2. There were no differences in body-weight gain or food intake between groups but fluid intake for the beer group was considerably higher than that for the other groups.

3. There was a significant effect of the type of alcoholic beverage consumed on whole-body 65Zn retention. Rats given whisky had a smaller daily loss of 65Zn than those given water, beer or cider. The ethanol group also showed a lower rate of 65Zn loss compared with the water group. The observed changes in whole-body 65Zn retention could be explained by an adverse influence of ethanol on Zn absorption from the diet.

4. Blood Hb and testes Zn concentration were similar in all groups but the type of liquid consumed influenced liver Fe levels. The cider group had the lowest liver Fe values and the ethanol group the highest values.

5. It is apparent from the present study that ethanol and alcoholic beverages affect Zn and Fe metabolism, but that the effects of ethanol are moderated by other components of the alcoholic beverages.

Type
Clinical and Human Nutrition papers: Studies Relevant to Human Nutrition
Copyright
Copyright © The Nutrition Society 1988

References

Ahmed, S. B. & Russell, R. M. (1982). Journal of Laboratory and Clinical Medicine 100, 211217.Google Scholar
Antonson, D. L. & Vanderhoof, J. A. (1983). Digestive Diseases and Sciences 28, 604608.CrossRefGoogle Scholar
Carey, M. A., Jones, J. D. & Gastineau, C. F. (1971). Journal of American Medical Association 216, 17661769.CrossRefGoogle Scholar
Charlton, R. W., Jacobs, P., Seftel, H. & Bothwell, T. H. (1964). British Medical Journal ii, 14271429.CrossRefGoogle Scholar
Dinsmore, W., Callender, M. E., McMaster, D., Todd, S. J. & Love, A. H. G. (1985). Digestion 32, 238242.CrossRefGoogle Scholar
Fairweather-Tait, S. J. & Wright, A. J. A. (1984). British Journal of Nutrition 51, 185191.CrossRefGoogle Scholar
Fairweather-Tait, S. J., Wright, A. J. A., Cooke, J. & Franklin, J. (1985). British Journal of Nutrition 54, 401413.CrossRefGoogle Scholar
Gillooly, M., Bothwell, T. H., Charlton, R. W., Torrance, J. D., Bezwoda, W. R., MacPhail, A. P., Derman, D. P., Novelli, L., Morrall, P. & Mayet, F. (1984). British Journal of Nutrition 51, 3746.CrossRefGoogle Scholar
Helwig, H. L., Hoffer, E. M., Thielen, W. C., Alcocer, A. E., Hotelling, D. R., Rogers, W. H. & Lench, J. (1966). American Journal of Clinical Pathology 45, 156159.CrossRefGoogle Scholar
Hillman, R. S. (1975). Annals of the New York Academy of Science 252, 297306.CrossRefGoogle Scholar
Kahn, A. M., Helwig, H. L., Redeker, A. G. & Reynolds, T. B. (1965). American Journal of Clinical Pathology 44, 426435.CrossRefGoogle Scholar
McDonald, J. T. & Margen, S. (1980). American Journal of Clinical Nutrition 33, 10961102.CrossRefGoogle Scholar
MacDonald, R. A. & Pechet, G. S. (1964). Proceedings of the Society of Experimental Biology and Medicine 117, 5456.CrossRefGoogle Scholar
Mills, P. R., Fell, G. S., Bessent, R. G., Nelson, L. M. & Russell, R. I. (1983). Clinical Science 64, 527535.CrossRefGoogle Scholar
Prasad, A. S., Oberleas, D., Wolf, P. & Horwitz, J. P. (1967). Journal of Clinical Investigation 46, 549557.CrossRefGoogle Scholar
Richterich, R. & Colombo, J. P. (1981). Clinical Chemistry, pp. 543546. Chichester: John Wiley & Sons..Google Scholar
Silverman, B. & Rivlin, R. S. (1982). Journal of Nutrition 112, 744749.CrossRefGoogle Scholar
Sorensen, E. W. (1966). Acta Medica Scandinavica 180, 241244.CrossRefGoogle Scholar
Sullivan, J. F. (1962). Quarterly Journal of Studies on Alcohol 23, 216220.CrossRefGoogle Scholar
Sullivan, J. F. & Lankford, H. G. (1965). American Journal of Clinical Nutrition 17, 5763.Google Scholar
Vallee, B. L., Wacher, W. E., Bartholomay, A. F. & Hoch, F. L. (1957). New England Journal of Medicine 257, 10551065.CrossRefGoogle Scholar