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Intestinal zinc transfer by everted gut sacs from rats given diets containing different amounts and types of dietary fibre

Published online by Cambridge University Press:  09 March 2007

C. J. Seal
Affiliation:
Department of Agricultural Biochemistry and Nutrition, University of Newcastle upon Tyne, Newcastle upon Tyne NE1 7RU
J. C. Mathers
Affiliation:
Department of Agricultural Biochemistry and Nutrition, University of Newcastle upon Tyne, Newcastle upon Tyne NE1 7RU
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Abstract

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Two experiments were carried out in which rats were offered diets containing different amounts and types of dietary fibre, i.e. commercial stock diet and three semi-purified diets containing no fibre, 200 g wheat bran or 200 g pectin/kg. Dietary inclusion of fibre, and especially pectin, stimulated large bowel fermentation, as indicated by caecal hypertrophy and reduced caecal pH. After 3 weeks, mucosal:serosal zinc transfer and Zn accumulation by tissue were measured using the everted-gut-sac technique. In Expt 2, incubations were carried out in the presence and absence of 0.25 mm-ouabain to assess the importance of transfer by Na+, K+-ATPase-dependent mechanisms, and some observations on glucose transport were also made. Ouabain reduced rates of transfer of both Zn and glucose and also tissue Zn accumulation. There were no significant differences in rates of Zn transfer by everted sacs from duodenal, ileal and colonic sites, but accumulation of Zn by tissue was a more important fate than transfer across the serosal surface, and accumulation by duodenal tissue was approximately twice as great as by other tissues. Mucosal:serosal transfer of glucose by ileal tissue was much more sensitive to ouabain than was Zn transfer. Previous diet appeared to alter the capacity of the intestinal tissue to transfer Zn, with the highest rates of transfer being by colonic tissue from pectin-fed rats.

Type
Research Article
Copyright
Copyright © The Nutrition Society 1989

References

REFERENCES

Aldor, T.A.M. & Moore, E.W. (1970). Magnesium absorption by everted sacs of rat intestine and colon. Gastroenterology 59, 745753.CrossRefGoogle ScholarPubMed
Ammann, P., Rizzoli, R. & Fleisch, H. (1986). Calcium absorption in the rat large intestine in vivo: availability of dietary calcium. American Journal of Physiology 251, G14G18.Google ScholarPubMed
Anderson, D.M.W., Busuttil, A., Kempson, S.A. & Penman, D.W. (1986). Transmission electron microscopy of jejunum, ileum, and caecum tissue from rats fed with gum arabic, karaya and tragacanth. Toxicology 41, 7582.CrossRefGoogle ScholarPubMed
Antonson, D.L., Barak, A.J. & Vanderhoof, J.A. (1979). Determination of the site of zinc absorption in rat small intestine. Journal of Nutrition 109, 142147.CrossRefGoogle ScholarPubMed
Arduser, F., Wolffram, S. & Scharrer, E. (1985). Active absorption of selenate by rat ileum. Journal of Nutrition 115, 12031208.CrossRefGoogle ScholarPubMed
Bertoni, G., Watson, M.J., Savage, G.P. & Armstrong, D.G. (1976). The movements of minerals in the digestive tract of dry and lactating Jersey cows. 2. Net movements of Cu, Fe, Mn and Zn. Zootecnica e Nutrizione Animale 11, 185191.Google Scholar
Brown, R.C., Kelleher, J. & Losowsky, M.S. (1979). The effect of pectin on the structure and function of the rat small intestine. British Journal of Nutrition 42, 357365.CrossRefGoogle ScholarPubMed
Cheng, B.-Q., Trimble, R.P., Illman, P.J., Stone, B.A. & Topping, D.L. (1987). Comparative effects of dietary wheat bran and its morphological components (aleurone and pericarp-seed coat) on volatile fatty acid concentrations in the rat. British Journal of Nutrition 57, 6976.CrossRefGoogle ScholarPubMed
Cousins, R.J. (1986). Zinc metabolism—coordinate regulation as related to cellular function. In Proceedings of the XIII International Congress of Nutrition, pp. 500–504 [Taylor, T.G. and Jenkins, N.K., editors]. London: John Libbey.Google Scholar
Cummings, J.H. (1981). Dietary fibre. British Medical Bulletin 37, 6570.CrossRefGoogle ScholarPubMed
Cummings, J.H. (1984). Constipation, dietary fibre and the control of large bowel function. Postgraduate Medical Journal 60, 811819.CrossRefGoogle ScholarPubMed
Cummings, J.H., Southgate,, D.A.T., Branch, W.J., Wiggins, H.S., Houston, H., Jenkins,, D.J.A., Jivraj, T. & Hill, M.J. (1979). The digestion of pectin in the human gut and its effects on calcium absorption and large bowel function. British Journal of Nutrition 41, 477485.CrossRefGoogle ScholarPubMed
Davies, N.T. (1980). Studies on the absorption of zinc by rat intestine. British Journal of Nutrition 43, 189203.CrossRefGoogle ScholarPubMed
Davies, N.T. & Nightingale, R. (1975). The effects of phytate on intestinal absorption and secretion of zinc and whole body retention of zinc, copper, iron and manganese in rats. British Journal of Nutrition 34, 243258.CrossRefGoogle ScholarPubMed
Davies, N.T. & Reid, H. (1979). An evaluation of the phytate, zinc, copper, iron and manganese contents of, and Zn availability from, soya-based textured-vegetable-protein meat-substitutes or meat-extenders. British Journal of Nutrition 41, 579589.CrossRefGoogle ScholarPubMed
Demigne, C. & Remesey, C. (1985). Stimulation of absorption of volatile fatty acids and minerals in the caecum of rats adapted to a very high fibre diet. Journal of Nutrition 115, 5360.CrossRefGoogle Scholar
Emes, J.H. & Arthur, D. (1975). The site of zinc absorption in the rat small intestine. Proceedings of the Society for Experimental Biology and Medicine 148, 8688.CrossRefGoogle ScholarPubMed
Englyst, H.N. & Cummings, J.H. (1984). Simplified method for the measurement of total non-starch polysaccharides by gas–liquid chromatography of constituent sugars as alditol acetates. Analyst 109, 937942.CrossRefGoogle Scholar
Englyst, H.N. & Cummings, J.H. (1985). Digestion of the polysaccharides of some cereal foods in the human small intestine. American Journal of Clinical Nutrition 42, 778787.CrossRefGoogle ScholarPubMed
Evans, G.W., Grace, C.I. & Hahn, C. (1973). Homeostatic regulation of zinc absorption in the rat. Proceedings of the Society for Experimental Biology and Medicine 143, 723725.CrossRefGoogle ScholarPubMed
Evans, G.W. & Johnson, E.C. (1981). Effect of iron, vitamin B6 and picolinic acid on zinc absorption in the rat. Journal of Nutrition 111, 6875.CrossRefGoogle ScholarPubMed
Fairweather-Tait, S.J. & Wright, A.J.A. (1985). The effect of ‘fibre-filler’ (F-plan diet) on iron, zinc and calcium absorption in rats. British Journal of Nutrition 54, 585592.CrossRefGoogle ScholarPubMed
Flanagan, P.R., Haist, J. & Valberg, L.S. (1983). Zinc absorption, intraluminal zinc and intestinal metallothionein levels in zinc-deficient and zinc-replete rodents. Journal of Nutrition 113, 962972.CrossRefGoogle ScholarPubMed
Ghishan, F.K. & Sobo, G. (1983). Intestinal maturation: in vivo zinc transport. Pediatric Research 17, 148151.CrossRefGoogle ScholarPubMed
Goodlad, J.S. & Mathers, J.C. (1988). Effects of food carbohydrates on large intestinal fermentation in vitro. Proceedings of the Nutrition Society 47, 176A.Google Scholar
Grace, N.D. (1975). Studies on the flow of zinc, cobalt, copper and manganese along the digestive tract of sheep given perennial ryegrass, or white or red clover. British Journal of Nutrition 34, 7382.CrossRefGoogle ScholarPubMed
Hoadley, J.E., Leinart, A.S. & Cousins, R.J. (1987). Kinetic analysis of zinc uptake and serosal transfer by vascularly perfused rat intestine. American Journal of Physiology 252, G825G831.Google ScholarPubMed
Jacobs, L.R. (1983). Modulation of mucosal cell proliferation in the intestine of rats fed a wheat bran diet. American Journal of Clinical Nutrition 37, 954960.CrossRefGoogle ScholarPubMed
James, W.P.T., Branch, W.J. & Southgate, D.A.T. (1978). Calcium binding by dietary fibre. Lancet i, 638.CrossRefGoogle Scholar
Key, F.B. & Mathers, J.C. (1987). Response of rat caecal metabolism to varying proportions of white and wholemeal bread. Proceedings of the Nutrition Society 46, 11A.Google Scholar
Kowarski, S., Blair-Stanek, C.S. & Schachter, D. (1974). Active transport of zinc and identification of zinc-binding proteins in rat jejunal mucosa. American Journal of Physiology 226, 401407.CrossRefGoogle ScholarPubMed
Lonnerdal, B., Stanislowski, A.G. & Hurley, L.S. (1980). Isolation of a low molecular weight zinc binding ligand from human milk. Journal of Inorganic Biochemistry 12, 7178.CrossRefGoogle ScholarPubMed
McCance, R.A. & Widdowson, E.M. (1942a). Mineral metabolism of healthy adults on white and brown bread dietaries. Journal of Physiology 101, 4485.CrossRefGoogle Scholar
McCance, R.A. & Widdowson, E.M. (1942b). Mineral metabolism on dephytinised bread. Journal of Physiology 101, 304313.CrossRefGoogle Scholar
Meneely, R. & Ghishan, F.K. (1982). In vivo intestinal zinc transport in rats: normal and growth retarded. Journal of Pediatric Gastroenterology and Nutrition 1, 119124.CrossRefGoogle ScholarPubMed
Methfessel, A.H. & Spencer, H. (1973). Zinc metabolism in the rat. Intestinal absorption of zinc. Journal of Applied Physiology 34, 5862.CrossRefGoogle ScholarPubMed
Oberleas, D., Muhrer, M.E. & O'Dell, B.L. (1966). Dietary metal-complexing agents and zinc availability in the rat. Journal of Nutrition 90, 5662.CrossRefGoogle ScholarPubMed
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, 304306.CrossRefGoogle ScholarPubMed
Partridge, I.G. (1978). Studies on digestion and absorption in the intestines of growing pigs. 4. Effects of dietary cellulose and sodium levels on mineral absorption. British Journal of Nutrition 39, 539545.CrossRefGoogle ScholarPubMed
Pearson, W.N., Schwink, T. & Reich, M. (1966). In vitro studies on zinc in the rat. In Zinc Metabolism, pp. 239–249 [Prasad, A.S., editor]. Springfield, Illinois: C. C. Thomas.Google Scholar
Sandstrom, B., Cederblad, A., Kivisto, B., Stenquist, B. & Anderson, H. (1986). Retention of zinc and calcium from the human colon. American Journal of Clinical Nutrition 44, 501504.CrossRefGoogle ScholarPubMed
Schiau, S.-Y. & Chang, G.W. (1986). Effects of certain dietary fibres on apparent permeability of the rat intestine. Journal of Nutrition 116, 223232.CrossRefGoogle Scholar
Seal, C.J. & Heaton, F.W. (1983). Chemical factors affecting the intestinal absorption of zinc in vitro and in vivo. British Journal of Nutrition 50, 317324.CrossRefGoogle ScholarPubMed
Seal, C.J. & Heaton, F.W. (1985). Effect of dietary picolinic acid on the metabolism of exogenous and endogenous zinc in the rat. Journal of Nutrition 115, 986993.CrossRefGoogle Scholar
Seal, C.J. & Heaton, F.W. (1987). Zinc transfer among proteins in rat duodenal mucosa. Annals of Nutrition and Metabolism 31, 5560.CrossRefGoogle Scholar
Seal, C.J. & Mathers, J.C. (1987). Na+-K+-ATPase-dependent zinc transfer by everted gut sacs from rats given different amounts and types of dietary fibre. Proceedings of the Nutrition Society 46, 54A.Google Scholar
Solomons, N.W. (1986). Zinc bioavailability to humans. In Proceedings of the XIII International Congress of Nutrition, pp. 504–508. [Taylor, T.G. and Jenkins, N.K., editors]. London: John Libbey.Google Scholar
Underwood, E.J. (1977). Zinc. In Trace Elements in Human and Animal Nutrition, 4th ed. New York: Academic Press.Google Scholar
Vahouny, G.V., Cassidy, M.M., Lightfoot, F., Grau, L. & Kritchevsky, D. (1981). Ultrastructural modifications of intestinal and colonic mucosa induced by free or bound bile acids. Cancer Research 41, 37643765.Google ScholarPubMed
Wapnir, R.A., Garcia-Aranda, J.A., Mevorach, E.K. & Lifshitz, F. (1985). Differential absorption of zinc and low molecular weight ligands in the rat gut in protein–energy malnutrition. Journal of Nutrition 115, 900908.CrossRefGoogle ScholarPubMed
Wilson, T.H. & Wiseman, G. (1954). The use of sacs of everted small intestine for the study of the transference of substances from the mucosal to the serosal surface. Journal of Physiology 123, 116125.CrossRefGoogle Scholar
Wise, A. (1983). Dietary factors determining the biological activities of phytate. Nutrition Abstracts and Reviews 53, 791806.Google Scholar
Wyatt, G.M., Bayliss, C.E. & Holcroft, J.D.A. (1986). A change in human faecal flora in response to inclusion of gum arabic in the diet. British Journal of Nutrition 55, 261266.CrossRefGoogle ScholarPubMed
Wyatt, G.M., Horn, N., Gee, J.M. & Johnson, I.T. (1988). Intestinal microflora and gastrointestinal adaptation in the rat in response to non-digestible dietary polysaccharides. British Journal of Nutrition 60, 197207.CrossRefGoogle ScholarPubMed