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Lowering dietary phosphorus concentrations reduces kidney calcification, but does not adversely affect growth, mineral metabolism, and bone development in growing rabbits

Published online by Cambridge University Press:  09 March 2007

J. Ritskes-Hoitinga*
Affiliation:
Biomedical Laboratory, Faculty of Health Sciences, University of Southern Denmark, Winsloewparken 23, DK-5000, Odense C, Denmark
H. N. A. Grooten
Affiliation:
Department of Laboratory Animal Science, Utrecht University, Utrecht, The Netherlands
K. J. H. Wienk
Affiliation:
Department of Laboratory Animal Science, Utrecht University, Utrecht, The Netherlands
M. Peters
Affiliation:
Central Animal Facility, Wageningen University, Wageningen, The Netherlands
A. G. Lemmens
Affiliation:
Department of Laboratory Animal Science, Utrecht University, Utrecht, The Netherlands
A. C. Beynen
Affiliation:
Department of Large Animal Medicine, Utrecht University, Utrecht, The Netherlands
*
*Corresponding author: Dr Merel Ritskes-Hoitinga, fax +45 65 90 68 21, email [email protected]
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Abstract

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New Zealand White rabbits were used to investigate the influence of increasing dietary P concentrations on growth performance, mineral balance, kidney calcification and bone development. The minimum dietary P requirement of 0·22% (National Research Council) is usually exceeded in commercial natural-ingredient chows, leading to undesirable kidney calcifications. In order to study the optimal dietary P level, rabbits were fed semi-purified diets with four different P levels (0·1, 0·2, 0·4, and 0·8%; w/w) at a constant dietary Ca concentration (0·5%) during an 8-week period. Body weight and growth were not influenced by the dietary P level. During two periods (days 20–23 and 48–51), faeces and urine were collected quantitatively for the analysis of Ca, Mg and P and balances were calculated. Increased dietary P intake caused increased urinary and faecal P excretion and P apparent absorption and retention. Faecal Ca excretion increased with higher dietary P levels, whereas urinary Ca excretion reacted inversely. The apparent absorption of Ca became reduced at higher dietary P concentrations, but Ca retention was unchanged. The response of Mg was in a similar direction to that of the Ca balance. Kidney mineral content increased with higher dietary P levels, indicating the presence of calcified deposits. Nephrocalcinosis became more severe in kidney cortex and medulla at increasing dietary P levels, as was confirmed by histological analysis. Femur bone length was not differentially influenced by dietary P. Bone density (g/cm3) of the femur diaphysis became significantly lower at the 0·8% dietary P level as compared with the 0·2% P group only. The bone Mg content was significantly increased on the 0·8% P diet, both in the diaphysis and epiphysis. Plasma P concentration increased and plasma Ca decreased with higher dietary P levels, whereas plasma Mg levels were unaffected. The present study shows that the current recommended minimum dietary P level of 0·2% for rabbits, as advised by the National Research Council in 1977, leads to a normal growth and bone development, but also causes some degree of kidney calcifications at a dietary Ca level of 0·5%. As the dietary P level of 0·1% virtually prevented kidney calcification and at the same time did not give evidence for any deleterious effects on growth and bone development, this indicates that the current recommended dietary P level for rabbits should be regarded as a maximum advisable concentration, and that a lower P level may be more optimal.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2004

References

Berg, D, Jackl, G, Kollmer, WE & Schmahl, W (1979) Calcium intestinal resorption and accumulation in the tissues during nutrition with a P-enriched diet. Calcif Tissue Int 27, Suppl., A3 Abstr.Google Scholar
Chapin, RE & Smith, SE (1967 a) Calcium requirement of growing rabbits. J Anim Sci 26, 6771.CrossRefGoogle ScholarPubMed
Chapin, RE & Smith, SE (1967 b) High phosphorus diets fed to growing rabbits. Cornell Vet 57, 492500.Google ScholarPubMed
Heinemann, WW, Ensminger, ME, Ham, WE & Oldfield, JE (1957) The effect of phosphate fertilization of alfalfa on growth, reproduction, and body composition of domestic rabbits. J Anim Sci 16, 467475.CrossRefGoogle Scholar
Hoek, AC, Lemmens, AG, Mullink, JWMA & Beynen, AC (1988) Influence of dietary calcium:phosphorus ratio on mineral excretion and nephrocalcinosis in female rats. J Nutr 118, 12101216.CrossRefGoogle ScholarPubMed
Jowsey, J & Balasubramaniam, P (1972) Effect of phosphate supplements on soft-tissue calcification and bone turnover. Clin Sci 42, 289299.CrossRefGoogle ScholarPubMed
Lang, J (1981) The nutrition of the commercial rabbit. Part 1. Nutr Abstr Rev 51B, 197225.Google Scholar
Mathieu, LG & Smith, SE (1961) Phosphorus requirements of growing rabbits. J Anim Sci 20, 510513.CrossRefGoogle Scholar
National Research Council(1977) The Nutrient Requirements of Rabbits. Washington, DC: National Academy of Sciences.Google Scholar
National Research Council(1995) Nutrient Requirements of Laboratory Animals. Washington, DC: National Academy of Sciences.Google Scholar
Ritskes-Hoitinga, J & Beynen, AC (1992) Nephrocalcinosis in the rat: a literature review. Prog Food Nutr Sci 16, 85124.Google ScholarPubMed
Ritskes-Hoitinga, J, Lemmens, AG, Danse, LHJC & Beynen, AC (1989) Phosphorus-induced nephrocalcinosis and kidney function in female rats. J Nutr 119, 14231431.CrossRefGoogle ScholarPubMed
Ritskes-Hoitinga, J, Mathot, JNJJ, Lemmens, AG, Danse, LH, Meijer, GW, Van Tintelen, G & Beynen, AC (1993) Long-term phosphorus restriction prevents corticomedullary nephrocalcinosis and sustains reproductive performance but delays bone mineralization in rats. J Nutr 123, 754763.CrossRefGoogle ScholarPubMed
Ritskes-Hoitinga, J, Mathot, JNJJ, Van Zutphen, LFM & Beynen, AC (1992) Inbred strains of rats have differential sensitivity to dietary phosphorus-induced nephrocalcinosis. J Nutr 122, 16821692.CrossRefGoogle ScholarPubMed
Schoenmakers, ACM, Ritskes-Hoitinga, J, Lemmens, AG & Beynen, AC (1989) The influence of dietary phosphorus restriction on calcium and phosphorus metabolism in rats. Int J Vitam Nutr Res 59, 200206.Google ScholarPubMed
Shoback, DM & Strewler, GJ (2000) Disorders of the parathyroids and calcium metabolism. In Pathophysiology of Disease, 3rd ed. pp., 405415 [McPhee, SJ, Lingappa, VR, Ganong, WF and Lange, JD, editors]. New York: McGraw-Hill.Google Scholar
Van der Meer, R, de Vries, H, West, CE & De Waard, H (1985) Casein-induced hypercholesterolemia in rabbits is calcium-dependent. Atherosclerosis 56, 139147.CrossRefGoogle ScholarPubMed
Zemel, MB (1988) Calcium utilization: effect of varying level and source of dietary protein. Am J Clin Nutr 48, 880883.CrossRefGoogle ScholarPubMed