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Effect of zinc deficiency on the weight, cellularity and zinc concentration of different skeletal muscles in the post-weanling rat*

Published online by Cambridge University Press:  09 March 2007

Mary J. O'Leary
Affiliation:
Department of Food Science and Nutrition, University of Minnesota, St Paul, Minnesota 55108 and Veterans Administration Medical Center, Minneapolis, Minnesota 55417, USA
C. J. McClaln
Affiliation:
Department of Food Science and Nutrition, University of Minnesota, St Paul, Minnesota 55108 and Veterans Administration Medical Center, Minneapolis, Minnesota 55417, USA
P. V. J. Hegarty
Affiliation:
Department of Food Science and Nutrition, University of Minnesota, St Paul, Minnesota 55108 and Veterans Administration Medical Center, Minneapolis, Minnesota 55417, USA
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Abstract

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Zinc-deficient (ZD), weight-restricted (WR), pair-fed (PF) and ad lib. -fed (AL) Sprague-Dawley male rats were killed after feeding the respective Zn-deficient and Zn-supplemented diets from 3 to 8 weeks of age. Animals killed at the start of the experiment served as a baseline control (BC).

Four different skeletal muscles – biceps brachii, soleus, plantaris and extensor digitorum longus (EDL) – were studied for changes in weight, the number and diameter of muscle fibres and Zn concentration.

The soleus muscle had the highest concentration of Zn. It was the only muscle to reduce its Zn concentration due to Zn deficiency.

There was a loss of muscle fibres during normal growth (groups BC v. AL) in the soleus muscle (P < 0.05). The estimated length of muscle and the diameter of the muscle fibres in all four muscles increased significantly (P < 0.001). Therefore postweanling growth appears to occur as a result of longitudinal and transverse increases in the dimensions of these muscles.

The reduction in muscle fibre number in ZD rats compared to BC animals may occur within the range of expected fibre loss during normal growth. Fibre loss in ZD rats may be more affected by feeding-pattern-dependent metabolic changes than by a deficiency of Zn per se (groups ZD v. WR). Soleus fibre loss in ZD rats may be related to the high Zn concentration in this muscle.

The effect of Zn deficiency per se on muscle fibre diameter may be inaccurately interpreted by comparing the ZD animals with their PF and AL controls. There was no significant difference in fibre diameter in any of the four muscles when ZD and WF rats were compared.

Type
Papers on General Nutrition
Copyright
Copyright © The Nutrition Society 1979

References

Ariano, M. A., Armstrong, R. B. & Edgerton, V. R. (1973). J. Histochem. Cytochem 21, 51.CrossRefGoogle Scholar
Bedi, K. S., Mahon, M. & Smart, J. L. (1978). Proc. Nutr. Soc. 37, 59A.Google Scholar
Bendall, J. R. & Voyle, C. A. (1967). J. Fd Technol. 2, 259.CrossRefGoogle Scholar
Bernhart, F. W. & Tomarelli, R. M. (1966). J. Nutr. 89, 495.CrossRefGoogle Scholar
Burleigh, I. G. (1974). Biol. Rev. 49, 267.CrossRefGoogle Scholar
Cassens, R. G., Hoekstra, W. G., Faltin, E. C. & Briskey, E. J. (1967). Am. J. Physiol. 212, 688.CrossRefGoogle Scholar
Chesters, R. K. & Quarterman, J. (1970). Br. J. Nutr. 24, 1061.CrossRefGoogle Scholar
Florence, E. & Quarterman, J. (1972). Br. J. Nutr. 28, 63.CrossRefGoogle Scholar
Greene, E. C. (1959). Anatomy of the Rat, p. 31. New York: Hafner.Google Scholar
Hambidge, M. K. & Walravens, P. A. (1976). In Trace Elements in Human Health and Disease. Vol. 1. Zinc and Copper, p. 21 [Prasad, A. S. and Oberleas, D., editors]. New York: Academic Press.Google Scholar
Heffron, J. J. A. & Hegarty, P. V. J. (1974). Comp. Biochem. Physiol. 49A, 43.CrossRefGoogle Scholar
Hsu, J. M. & Anthony, W. L. (1975). J. Nutr. 105, 26.CrossRefGoogle Scholar
Huber, A. M. & Gershoff, S. N. (1973). J. Nutr. 103, 1175.CrossRefGoogle Scholar
Inokuchi, S., Ishikawa, H., Iwamoto, S. & Kimura, T. (1975). Hum. Biol. 47, 231.Google Scholar
Kang, H. K., Harvey, P. N., Valentine, J. L. & Swendseid, M. E. (1977). Clin. Chem. 23, 1834.CrossRefGoogle Scholar
Kim, K. O. & Hegarty, P. V. J. (1978). Proc. Nutr. Soc. 37, 114A.Google Scholar
Kirchgessner, M., Roth, H. P., Spoeri, R., Schnegg, A., Kellner, R. J. & Weigand, E. (1977). Nutr. Metab. 21, 119.CrossRefGoogle Scholar
Layman, D. K. (1978). Biochemical and morphological changes in skeletal muscle fibers during normal growth and prolonged starvation. PhD Thesis, University of Minnesota.Google Scholar
Layman, D. K., Hegarty, P. V. J. & Swan, P. B. (1979). J. Anat. (In the Press).Google Scholar
Lee, G. L. (1968). Manual of Histologic Staining Methods, 3rd ed., p. 94. New York: McGraw-Hill.Google Scholar
Miller, E. R., Luecke, R. W., Ullrey, D. E., Baltzer, B. V., Bradley, B. L. & Hoefer, J. A. (1968). J. Nurr. 95, 278.Google Scholar
Montgomery, R. D. (1962). J. Clin. Path. 15, 511.CrossRefGoogle Scholar
Prasad, A. S. (1976). In Trace Elements in Human Health and Disease. Vol. 1. Zinc and Copper, p. 1 [Prasad, A. S. and Oberleas, D., editors]. New York: Academic Press.Google Scholar
Rayne, J. & Crawford, G. N. C. (1975). J. Anat. 119, 347.Google Scholar
Rowe, R. W. D. (1968). J. exp. Zool. 167, 353.CrossRefGoogle Scholar
Rowe, R. W. D. & Goldspink, G. (1969). J. Anat. 104, 519.Google Scholar
Sandstead, H. H. (1973). Am. J. clin. Nutr. 26, 1251.CrossRefGoogle Scholar
Stickland, N. C., Widdowson, E. M. & Goldspink, G. (1975). Br. J. Nurr. 34, 421.CrossRefGoogle Scholar
Thompson, E. H., Levine, A. S., Hegarty, P. V. J. & Allen, C. E. (1979). J. Anim. Sci. 48, 328.CrossRefGoogle Scholar
Underwood, E. J. (1977). In Trace Elements in Human and Animal Nutrition. New York: Academic Press.Google Scholar