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Effect of dietary calcium level on mineral and trace element utilization from a rapeseed (Brassica napus L.) diet fed to ileum-fistulated pigs

Published online by Cambridge University Press:  09 March 2007

Torben Larsen
Affiliation:
National Institute of Animal Science, Animal Physiology and Biochemistry, Foulum, PO Box 39, 8830 Tjele, Denmark
Brittmarie Sandstrom
Affiliation:
Research Department of Human Nutrition, Royal Veterinary and Agricultural University, Rolighedsvej 25, DK-1958 Frederiksberg C, Denmark
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Abstract

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The bioavailability of intrinsic minerals in rapeseed (Brassica napus L.) meal was studied in growing, fistulated pigs. Furthermore, the effect on mineral availability of an extrinsic Ca supply to this diet, high in phytate, was observed. Comparisons between small intestinal and total gastrointestinal absorption were accomplished for minerals and other dietary components. N retention increased as the dietary Ca intake increased, but dropped, in general significantly, throughout the experimental period, indicating that factors other than protein were limiting for growth. The highest dietary Ca level increased the absorption and retention of Ca and Mg. In contrast, addition of CaCO3 did not influence the apparent absorption and retention of P, Fe, Zn, Cu and Mn. The majority of observed blood variables was not affected by the Ca content of the diet. Zn status-related variables were, however, thoroughly depressed by duration of the experiment and it seems probable that the amount of absorbed Zn was a factor limiting growth. Total gastrointestinal balances showed a Zn retention of 4.7 mg/d, which accounted for 13.6 % of that ingested. This low absorption of Zn may have been due to the high intrinsic content of phytate. Apparent absorption of organic matter, ash, N and S was significantly greater calculated from faecal contents than from ileal contents, indicating a disappearance of material in the caecum–colon section of the gastrointestinal tract. The minerals which were studied showed the opposite pattern: apparent small intestinal absorption was larger than total intestinal absorption, suggesting that the caecal–colon region takes part in mineral turnover.

Type
Effects of Diet on Trace Element Nutriton
Copyright
Copyright © The Nutrition Society 1993

References

REFERENCES

Agergaard, N. (1979). Alkaline phosphatase in pigs. Studies of alkaline phosphatase isoenzymes in blood and tissues. Thesis. The Royal Veterinary and Agricultural University, Copenhagen, Denmark.Google Scholar
Boisen, S. (1987). Fytinsyre og fytaseaktivitet i foderstoffer. National Institute of Animal Science. Communication no. 675. Foulum DK-8833, Denmark: National Institute of Animal Science.Google Scholar
Borg Jensen, B. (1987). Effect of feed composition on the microbial activity in various segments of the digestive tract of pigs. Proceedings of 38th Annual Meeting of the European Association for Animul Production, Lisbon, p. 362. Rome: EAAP.Google Scholar
Bowers, G. N. & McComb, R. B. (1975). Measurement of total alkaline phosphatase activity in human serum. Clinical Chemistry 21, 1988 1995.CrossRefGoogle ScholarPubMed
Cousins, R. J. (1985). Absorption, transport, and hepatic metabolism of copper and zinc: special reference to metallothionein and ceruloplasmin. Physiological Reviews 65, 238309.CrossRefGoogle ScholarPubMed
Davies, N. T., Carswell, A. J. P. & Mills, C. F. (1985). The effects of variation in dietary calcium intake on the phytate-zinc interaction in rats. In Trace Elements in Man and Animals TEMA 5, p. 456 [Mills, C. F., Bremner, I. and Chesters, J. K., editors]. Farnham Royal: C.A.B. Publications.Google Scholar
Davies, N. T. & Olpin, S. E. (1979). Studies on the phytate: zinc molar concentrations in diets as a determinant of Zn availability to young rats. British Journal of Nutririon 41, 591603.CrossRefGoogle ScholarPubMed
Fordyce, E. J., Forbes, R. M., Robbins, K. R. & Erdman, J. W. Jr (1987). Phytate*calcium/zinc molar ratios: are they predictive of zinc bioavaihbility. Journal of Food Science 52, 440444.CrossRefGoogle Scholar
Foster, D. M., Aamodt, R. L., Henkin, R. I. & Berman, M. (1979). Zinc metabolism in humans: a kinetic model. Americun Journui of Physiology 237, R 340–R 349.Google ScholarPubMed
Hoekstra, W. G., Faltin, E. C., Lin, C. W., Roberts, H. F. and Grummer, R. H. (1967). Zinc deficiency in reproducing gilts fed a diet high in calcium and its effect on tissue zinc and blood serum alkaline phosphatase. Journal of Animal Science 26, 13481357.CrossRefGoogle ScholarPubMed
Just, A., Jsrgensen, H., Fernandez, J. A., Bech-Andersen, S. & Enggaard Hansen, N. (1983). The chemical composition, digestibility, energy and protein value of different feedstuffs for pigs. Beretning fra Statens Husdyrbrugsforsøg no. 556. Copenhagen: National Institute for Animal Science.Google Scholar
Low, A. G., Partridge, I. G. & Sambrook, I. E. (1978). Studies on digestion and absorption in the intestines of growing pigs. 2. Measurements of the flow of dry matter, ash and water. British Journal of Nutririon 39, 515526.CrossRefGoogle ScholarPubMed
Luecke, R. W., Hoefer, J. A., Brammel, W. S. & Schmidt, D. A. (1957). Calcium and zinc in parakeratosis of swine. Journal of Animal Science 16, 311.CrossRefGoogle Scholar
Leucke, R. W., Hoefer, J. A., Brammel, W. S. & Thorp, F. Jr (1956). Mineral interrelationship in parakeratosis of swine. Journal of Animal Science 15, 347351.CrossRefGoogle Scholar
Moore, J. H. & Tyler, C. (1955 a). Studies on the intestinal absorption and excretion of calcium and phosphorus in the pig. 1. A critical study of the Bergeim technique for investigating the intestinal absorption and excretion British Journal of Nutrition 9, 8193.CrossRefGoogle ScholarPubMed
Moore, J. H. & Tyler, C. (1955 b). Studies on the intestinal absorption and excretion of calcium and phosphorus in the pig. 2. The intestinal absorption and excretion of radioactive calcium and phosphorus. British Journal of Nutrition 9, 8193.CrossRefGoogle ScholarPubMed
Morris, E. R. & Ellis, R. (1980). Effect of dietary phytate/zinc molar ratio on growth and bone zine response of rats fed semipurified diets. Journal of Nutrition 110, 10371045.CrossRefGoogle Scholar
Nes, P. (1979). Routine measurements of total sulphur in biological material. New Zealand Journal of Science 22, 269272.Google Scholar
Oberleas, D., Muhrer, M. E. & O'Dell, B. L. (1962). Effects of phytic acid on zinc availability and parakeratosis in swine. Journal of Animal Science 21, 5761.CrossRefGoogle Scholar
O'Dell, B. L. & Savage, J. E. (1957). Potassium, zinc and distillers dried solubles as supplements to a purified diet. Poultry Science 36, 459460.CrossRefGoogle Scholar
O'Dell, B. L. & Savage, J. E. (1960). Effect of phytic acid on zinc availability. Proceedings of the Society for Experimental Biology and Medicine 103, 304 306.Google ScholarPubMed
O'Dell, B. L., Yohe, J. M. & Savage, J. E. (1964). Zinc availability in the chick as affected by phytate, calcium and ethylenediaminetetraacetate. Poultry Science 43, 415419.CrossRefGoogle Scholar
Pierce, A. B., Doige, C. E., Bell, J. M. & Owen, B. D. (1977). Availability of phytate phosphorus to the growing pig receiving isonitrogenous diets based on wheat or corn. Canadian Journal of Anitnal Science 57, 573583.CrossRefGoogle Scholar
Pointillart, A. (1985). Magnesium metabolism in the growing pig. Magnesium Deficiency. First European Congress on Magnesium, Lisbon, pp. 6365. [Halpern, M. J. and Durlach, J, editors ]. Basel: Karger.CrossRefGoogle Scholar
Pointillart, A., Fourdin, A. & Fontaine, N. (1987). Importance of cereal phytase activity for phytate phosphorus utilization by growing pigs fed diets containing triticale or corn. Journal of Nutrition 117, 907913.CrossRefGoogle ScholarPubMed
Sandberg, A.-S. & Ahderinne, R. (1986). HPLC method for determination of inositol tri-, tetra-, penta-, and hexaphosphates in foods and intestinal content. Journal of Food Science 51, 547550.CrossRefGoogle Scholar
Sandberg, A.-S. & Andersson, H. (1988). Effect of dietary phytase on the digestion of phytate in the stomach and small intestine of humans. Journal of Nutrition 118, 469473.CrossRefGoogle ScholarPubMed
SandbergA,-S. A,-S., Anderson, H., Carlsson, N.-G. & Sandström, (1987). Degradation products of bran phytate formed during digestion in the human small intestine: effects of extrusion cooking on digestibility. Journal of Nutrition 117, 20612065.CrossRefGoogle ScholarPubMed
Sandström, B., Cederblad, Å., Kivisto, B., Stenquist, B. & Andersson, H. (1986). Retention of zinc and calcium from the human colon. Americun Journal of Clinical Nutrition 44, 501504.CrossRefGoogle ScholarPubMed
SAS Institute Inc. (1985). SAS Users Guide: Stutisticaf Version 5. Cary, N. C.: SAS Institute Inc.Google Scholar
Smith, W. H., Plumlee, M. P. & Beeson, W. M. (1962). Effect of source of protein on zinc requirement of the growing pig. Journal of Animal Science 21, 399405.CrossRefGoogle Scholar
Stuffins, C. B. (1967). The determination of phosphate and calcium in feeding stuffs. Analyst 92, 107111.CrossRefGoogle ScholarPubMed
Sullivan, J. F., Williams, R. V., Wisecarver, J., Etzel, K., Jetton, M. M. & Magee, D. F. (1981). The zinc content of bile and pancreatic juice in zinc-deficient swine. Proceedings of the Society for Experimental Biology and Medicine 116, 3943.CrossRefGoogle Scholar
Tucker, H. F. & Salmon, W. D. (1955). Parakeratosis or zinc deficiency disease in the pig. Proceedings ofSociety for Experimental Biology and Medicine 88, 613616.CrossRefGoogle ScholarPubMed
Whiting, F. & Bezeau, L. M. (1958). The calcium, phosphorus and zinc balance in pigs as influenced by the weight of pigs and the level of calcium, zinc and vitamin D in the ration. Canadian Journal of Animal Science 38, 109117.CrossRefGoogle Scholar