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Effect of level of dietary calcium on the skeleton of the rat

Published online by Cambridge University Press:  09 March 2007

Joyce Toothill
Affiliation:
National Institute for Research in Dairying, Shinfield, Reading
Zena D. Hosking
Affiliation:
National Institute for Research in Dairying, Shinfield, Reading
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Abstract

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1. The total body calcium (Expt 1) of litter-mate male rats given a diet adequate in phosphorus and high (0·74%) or low (0·13%) in Ca from the age of 3 weeks was determined after 21, 48 and 60 weeks on the diet. In Expt 2, the ash content of ten groups of bones from 10-week-old rats given these same diets for 7 weeks was studied to ascertain whether all groups were equally affected by the difference in dietary Ca level. Four groups of bones, i.e. skull and mandibles, vertebras, the shafts and the ends of long bones, were consequently chosen for examination in Expt 3 where their growth and composition were studied in rats given the Ca diets for 24, 48 or 60 weeks from the age of 3 weeks.

2. Total body Ca (Expt 1), expressed as g Ca or as a percentage of the net body-weight or of net dry, fat-free carcass weight, was always significantly higher in rats given the higher level of Ca. The dietary effect was greatest after 21 weeks.

3. The higher level of dietary Ca led to a highly significant increase in the weight of the dry, fat-free bone and in the percentage ash content of all ten bone groups after 7 weeks (Expt 2). The greater treatment differences in ash content occurred with the less well mineralized bones.

4. In Expt 3, irrespective of diet, the four groups of bones developed at different rates. In rats given the diets for 24 weeks or longer, the vertebras and the shafts of long bones showed the greatest proportional increase in weight of dry, fat-free bone and ash relative to the corresponding values for 3-week-old rats; the greatest change in percentage ash content occurred in the ends of the long bones.

5. Increasing the level of Ca in the diet increased the weight of the dry, fat-free bone and its ash content. The effect of diet decreased with increasing time on the diets, in general persisting most strongly in the skull and mandibles and declining most rapidly in the ends of the long bones. The percentage Ca and P content of the bone ash was only slightly affected by diet and, except for the Ca in the ash of vertebras, significant differences were only found in the composition of the ash of bones from 27-week-old rats.

Type
Research Article
Copyright
Copyright © The Nutrition Society 1968

References

Benzie, D., Boyne, A. W., Dalgarno, A. C., Duckworth, J., Hill, R. & Walker, D. M. (1955). J. agric. Sci., Camb. 46, 425.CrossRefGoogle Scholar
Bessey, O. A., King, C. G., Quinn, E. J. & Sherman, H. C. (1935). J. biol. Chem. 111, 115.CrossRefGoogle Scholar
Blair, R. & Benzie, D. (1964). Br. J. Nutr. 18, 91.CrossRefGoogle Scholar
Blair, R., Diack, J. R. B. & MacPherson, R. M. (1963). Br. J. Nutr. 17, 19.CrossRefGoogle Scholar
de Loureiro, J. A. (1931). Archivo Patol. 3, 72.Google Scholar
Ellinger, G. M., Duckworth, J., Dalgarno, A. C. & Quenouille, M. H. (1952). Br. J. Nutr. 6, 235.CrossRefGoogle Scholar
Hanson, W. C. (1950). J. Sci. Fd Agric. 1, 172.CrossRefGoogle Scholar
Henry, K. M. & Kon, S. K. (1953). Br. J. Nutr. 7, 147.CrossRefGoogle Scholar
Henry, K. M., Kon, S. K., Todd, P. E. E., Toothill, J. & Tomlin, D. H. (1960). Acta biochim. pol. 7, 167.Google Scholar
Kitson, R. E. & Mellon, M. G. (1944). Ind. Engng Chem. analyt. Edn 16, 379.CrossRefGoogle Scholar
Lanford, C. S., Campbell, H. L. & Sherman, H. C. (1941). J. biol. Chem. 137, 627.CrossRefGoogle Scholar
Lanford, C. S. & Sherman, H. C. (1938). J. biol. Chem. 126, 381.CrossRefGoogle Scholar
McCrudden, F. H. (1911). J. biol. Chem. 10, 187.CrossRefGoogle Scholar
McKinlay, H. (1951). J. Anim. Techns Ass. 2, no. 2, p. 2.Google Scholar
Menczel, J., Schraer, R., Pakis, G., Posner, A. S. & Likins, R. C. (1963). Proc. Soc. exp. Biol. Med. 112, 128.CrossRefGoogle Scholar
Mitchell, H. H., Hamilton, T. S., Steggarda, F. R. & Bean, H. W. (1945). J. biol. Chem. 158, 625.CrossRefGoogle Scholar
Schraer, H., Siar, W. J. & Schraer, R. (1963). Archs Biochem. Biophys. 100, 393.CrossRefGoogle Scholar
Sherman, H. C. & Booher, L. E. (1931). J. biol. Chem. 93, 93.CrossRefGoogle Scholar
Sherman, H. C. & MacLeod, F. L. (1925). J. biol. Chem. 64, 429.CrossRefGoogle Scholar
Taylor, T. G. & Moore, J. H. (1954). Br. J. Nutr. 8, 112.CrossRefGoogle Scholar
Toepfer, E. W. & Sherman, H. C. (1936). J. biol. Chem. 115, 685.CrossRefGoogle Scholar
Whitcher, L. B., Booher, L. E. & Sherman, H. C. (1936). J. biol. Chem. 115, 679.CrossRefGoogle Scholar
Williams, D. E., Mason, R. L. & McDonald, B. B. (1964). J. Nutr. 84, 373.CrossRefGoogle Scholar